Engineering Materials & Conc. Tech
Engineering Materials & Conc. Tech
COURSE:
(NDBCE, NDWSE & NDA)
YEAR I
SEMESTER I
Civil engineering is concerned with the design, construction, supervision, maintenance, repair
and demolition or recycling of the various components of the buildings, bridges, canals, roads,
dams, tunnel etc. there is therefore need to have good knowledge of materials to be used.
Thedesign, construction, maintenance, repair and demolition or recycling in engineering forms
the life cycle of a structure or building. Normally the key element in the filed practice is to deal
with different types of materials and their properties. Engineers must be able to select and use
materials and analyses their failure under varying conditions.This entails drawing up detail
specifications, selecting the materials and testing them for acceptance etc.
A number of decisions must be made when selecting materials to be incorporated into a design
which includes whether:
The materials can consistently be formed into the correct shape and dimensional tolerance
A material is compatible with and can be easily joined to other parts of an assembly (the
assembly in this context being an engineering structure).
Must have the correct properties for production and for subsequent use.
Must not fail in use, producing a liability i.e.the material must not fail under loads imposed on
the structure and must not deflect excessively.
The material must not degrade significantly during the intended life of the structure. The other
criterion could be water tightness, speed of construction, aesthetic considerations.
The cost of the processed material must be acceptable. The estimated cost of the structure must
not exceed the available money. Usually the cheapest design ischosen, however a correct
The choices of materials must be compatible with the environmental standards from raw
materials sources through manufacturing through product usage and to eventual discard.
If he / she are to effectively participate in the design of reliable and economical building and
civil engineering components, structures, systems and processes that use the wide spectrum of
materials
Engineering materials deals with the study of materials in respect of the following:
1. Civil engineering materials Examples: clay and its products, cement, lime, concrete,
mortar, timber etc.
2. Electrical engineering materials Examples copper, aluminium, iron and steel etc
3. Mechanical engineering materials Examples Cast iron, steel, lubricating materials etc.
The following properties of materials will be discussed; physical and mechanical properties of
engineering materials.
1. Density:
Density is defined as mass per unit volume for a material. The derived unit usually used by
engineers is the kg/m3. Relative density is the density of the material compared with the density
of the water at 4°C.
The formulae of density and relative density are:
Density (p) = Mass (m)/volume (V)
2. Electrical Conductivity:
Figure shows a piece of electrical cable. In this example copper wire has been chosen for the
conductor or core of the cable because copper has the property of very good electrical
conductivity.
Semiconductor materials are capable of having their conductors properties changed during
manufacture. Examples of semiconductor materials are silicon and germanium. They are used
extensively in the electronics industry in the manufacture of solid-state devices such as diodes,
thermistors, transistors and integrated circuits.
5. Thermal Conductivity:
This is the ability of the material to transmit heat energy by conduction. Figure shows a soldering
iron. The bit is made from copper which is a good conductor of heat and so will allow the heat
energy stored in it to travel easily down to the tip and into the work being soldered. The wooden
handle remains cool as it has a low thermal conductivity and resists the flow of heat energy.
6. Fusibility:
This is the ease with which materials will melt. It can be seen from figure that solder melts easily
and so has the property of high fusibility. On the other hand, fire bricks used for furnace linings
only melt at very high temperatures and so have the properties of low fusibility.
Such materials which only melt a very high temperatures are called refractory materials. These
must not be confused with materials which have a low thermal conductivity and used as thermal
The good magnetic conductors have low reluctance and examples are the ferromagnetic
materials which get their name from the fact that they are made from iron, steel and associated
alloying elements such as cobalt and nickel. All other materials are non-magnetic and offer a
high reluctance to the magnetic flux felid.
8. Temperature Stability:
Any changes in temperature can have very significant effects on the structure and properties of
materials. However, there are several effects can appear with changes in temperature such as
creep.For example gas-turbine blades. The creep rate increases if the temperature is raised, but
becomes less if the temperature is lowered.
2. Toughness:
It is the ability of the materials to withstand bending or it is the application of shear stresses
without fracture, so the rubbers and most plastic materials do not shatter, therefore they are
tough. For example, if a rod is made of high-carbon steel then it will be bend without breaking
under the impact of the hammer, while if a rod is made of glass then it will broke by impact
loading.
3. Malleability:
It is the capacity of substance to withstand deformation under compression without rupture or the
malleable material allows a useful amount of plastic deformation to occur under compressive
loading before fracture occurs. Such a material is required for manipulation by such processes as
forging, rolling and rivet heading.
4. Hardness:
It is the ability of a material to withstand scratching (abrasion) or indentation by another hard
body, it is an indication of the wear resistance of the material.
The ball only makes a small indentation in the hard material but it makes a very much deeper
impression in the softer material.
6. Stiffness:
It is the measure of a material‘s ability not to deflect under an applied load.
For example, steel is very much stronger than cast iron, then the cast iron is preferred for
machine beds and frames because it is more rigid and less likely to deflect with consequent loss
of alignment and accuracy.
8. Elasticity:
It is the ability of a material to deform under load and return to its original size and shape when
the load is removed. If it is made from an elastic material it will be the same length before and
after the load is applied, despite the fact that it will be longer whilst the load is being applied. All
materials possess elasticity to some degree and each has its own elastic limits.
9. Plasticity:
Under such conditions the material takes a permanent set and will not return to its original size
and shape when the load is removed. When a piece of mild steel is bent at right angles into the
shape of a bracket, it shows the property of plasticity since it does not spring back strength again.
10. Creep:
The permanent deformation (strain) of a material under steady load as a function of time is called
creep. Length of our waist belt increases after some duration is due to creep effect.
11. Fatigue:
The behavior of materials under fluctuating and reversing loads (or stresses) is termed as fatigue.
This behaviour is different from that under the steady load. Fatigue is, however, not a dynamic
effect. The rate of loading is usually not a factor is fatigue behavior. Fatigue behavior is
experienced by all materials whether metals, plastics, concretes, or composites.
1.0. Soils
Introduction
Every work of construction in civil engineering is built on soil or rock and in many instances are
also the raw materials of construction. The study of soil and rock materials is an important part
of a wider area of study often geotechnical engineering. There is no clear dividing line between
the areas of study of soil as a material and soil mechanics, and both are equally important.
Soil is the relatively loose mass of mineral and organic materials and sediments found above the
bedrock, which can be relatively easily broken down into its constituent mineral or organic
particles.
In civil engineering usage, the term soil describes the uncemented or weakly cemented material
overlaying the harder rock on the planet‘s surface. Soils exist in great variety and are the
accumulated result of May separate factors and process. Their characteristics depend on the
parent rocks from which they are derived; on the means of these rocks and the weathering of the
soils itself at its various stages of formation; on the means of transport bringing the soil in its
present location; on the manner of deposition of the soil; on its history of loading, drainage,
wetting and drying and on many other processes.
The parent rocks themselves occur in great variety. The rock may have formed by the cooling
and hardening of a molten material, this group being termed igneous rocks. The igneous rocks
Types of soils
Residual soils
When rocks are weathered and the product accumulates in place, without transport occurring the
products are described as residual soils. In a sense the humus bearing top soils and weathered
subsoils of any formation are residual soils but the term is usually used for rock products such as
laterites. Significant thicknesses of these soils are found in various parts of the world and from
their distribution it appears that the warm humid regions are not favorable to the kind of
weathering that produces residual soils.
Transported soils.
Glacially transported soils; this is common in cold hilly countries like Britain and the
Scandinavian countries where glacier (ice) runs down slopes wearing away the surface particles
and depositing them down the streams or low lying areas. Some of the glacial debris transported
will melt to water before final deposition and as a result of this is likely to be sorted in\to size
groups of sands and gravels stratified after the manner of the river deposits.
Water transported soils; soils formed by water-borne material tend to very erratically in
physical properties from place to place and depth, a consequence of the continual changes
occurring in the streams and rivers which formed them. Fast - flowing steep streams in mountain
areas transport al but the stages rock fragments down steam and the fragments become
progressively broken up, worn and deposited. As the steepness of the steam diminishes the larger
The mechanical process of abrasion and grinding accounts for most of the reduction in particle
sizes from the fragments of the parent rocks.
Soils transported by man; in the consideration of soils in relation to engineering works man
himself should be included as an agent of transportation. Soils which have been excavated from
one place and transported to and placed in another place are described as fills. Fills may be
materials other than soils.
To consider soils among the other civil engineering materials it is necessary to distinguish the
principal soil groups one from another as with other materials, to establish parameters by which
the behavior of soils can be described quantitatively. Engineering characteristics such as
permeability, compressibility and strength usually differ in value from point to point in a soil
mass and at any one point these characteristics differ with the direction in which they are
measured. Soils showing this behavior are described as anisotropic. If the characteristics were
practically unvarying in value through out a soil, it would be described as isotropic.
Many soils show a fabric of laminations, varves, fissures, organic matter or root networks. A
quantitative description of the engineering characteristics of a particular soil stratum taking
account of these features of fabric should apply convincing to the whole stratum as it exists in
activity of the civil or geotechnical engineer, namely site investigation or more particularly soil
exploration.
Given that all existing information about a site has been assembled, the extent of exploration will
depend on the character of the ground and the type of construction work to be under taken.
Geological and geographical mapping will supplement existing data and enable further water
condition are sufficiently described to allow safe and economical project design. The lateral
Soil profile
The results of a soil exploration are often presented in the form of a soil profile. Astone which is
distinguishable from the ground surface to the limit of depth of exploration is called the soil
profile. The variation with depth, of any property of the soil for example, water content or
density may be displayed by the curve as shown below.
V= VS + VW + Vair
Where;
Also; V = VS + Vv, is the absolute volume of solids or pore spaces in the sample.
The samediagrammatic form is suited to presenting the masses of the constituents of the sample
thus
M = MS + MW
Where;
PHASE RELATIONSHIP
Soils are generally composed of three distinct phases. These are solids, water and air. The space
occupied by water and air is defined as the void of the soil. The void may be partially or wholly
filled by water or air. A completely dry or completely saturated soil will have only two phases.
The components parts may be illustrated as shown by a phase diagram.
Porosity (n)
This is the ratio of the volume of voids to the total volume;
Bulk Density
Is the ratio of the total mass of soil to the total volume of the soil.
The term consistency refers to the relative ease with which a soil mass can be deformed and is
used to describe the degree of firmness of fine-grained soils for which consistency relates to a
large extent to water content. The four states of consistency suggested by Atterberg are indicated
below;
1. Casagrande Apparatus
The apparatus consists of a mechanical device consisting of a cup mounted on an edge pivot. The
cup rests on a hard rubber base. A mechanism enables the cup to be lifted by 10mm and dropped
on the base. The soil is put in cup and leveled off horizontally. The soil is divided by a standard
grooving tool through the pivot of the cup. The two halves of the soil flow together as the cup is
repeatedly dropped onto the base. The number of drops at the rate of two revolutions per second
required to close the groove over a distance of 13mm is recorded. The test is repeated over four
times and the water content is determined each time. The water content is plotted against log of
blows. The best straight line fitting the points is drawn. The moisture content at twenty five (25)
blow is the Liquid Limit of the soil.
To obtain the liquid limit, cone penetration is plotted against moisture content both on normal
scales to give the best fitting straight line. The moisture content corresponding to a cone
penetration of 20mm is taken as the liquid limit of the soil, which for all practical purposes is the
same as the LL determined by the Casagrande apparatus.
The Cone Penetrometer method gives a more consistent estimate of the LL than the Casagrande
apparatus, with greater repeatability and less operator susceptibility.
Shrinkage limit, ws
PARTICLE-SIZE DISTRIBUTION
The soil grading or the distribution of particle size is quantitatively determined by performing the
particle-size analysis, also called mechanical analysis, which is carried out in two parts: sieve
analysis and sedimentation analysis. The distribution of gravel and sand particles is determined
by sieve analysis and that of silt and clay by sedimentation analysis. Depending on the type of
soil and the extent of particle-size distribution required, mechanical analysis may involve both
sieving and sedimentation or it may be restricted to either of them. For gravel and sand, sieve
analysis alone will suffice, but if silt and clay are present, a combined sieve and sedimentation
analysis may be required. If soil is predominantly silty and or clayey, sedimentation alone will
do.
Procedure;
i. Oven-dry sample.
ii. Crush the oven-dried sample using rubber pestle and mortar.
iii. Determine mass of sample and label as Wtotal in (g).
iv. Then prepare a stack of sieve aperture sizes with larger opening sizes at the top and down to
the last one with smaller opening sizes.
v. Pour the soil slowly into the stack of sieves from the top and place the cover, put the stack
onto the sieve shaker (vibrator), tighten the clamps, adjust the time with 5 to 10 minutes and turn
it on.
vi. When time is out, take out and measure the mass of retained soil inside, from the top sieve
until the pan.
% Retained
Find cumulative percent of aggregate retained in each sieve.
Then % Cumulative Passing = 100% - % Cumulative Retained.
The position and general shape and slope of a curve indicate type and grading of the soil.
A curve lying higher up or to the left represents relatively finer material.
The gradation of soil is said to be either well graded or poorly graded.
A soil is well graded when there is a good representation of all the particle sizes from the
largest to the smallest.
A soil is poorly graded if there is an excess or a deficiency of certain particle sizes within
the limits of the minimum and maximum sizes, or if most of the particles are of about the
same sizes (uniformly graded).
D10 : Maximum size of the smallest 10% D10 : Effective size ( e.g. for permeability)
D30: Maximum size of the smallest 30% Cu : Coefficient of Uniformity = D60/D10
D50 : Maximum size of the smallest 50% Cc : Coefficient of Curvature = (D30)2/(D60*D10)
D60 : Maximum size of the smallest 60% (also called Cg : Coefficient of Gradation)
To be well graded, Cc must lie within 1 and 3 and in addition, Cu must be greater than 4 for
gravels and greater than 6 for sands. If all particles are of the same size, Cu is unity.
A low value of Cu indicates a uniform soil and a high value a well graded soil.
SOIL DESCRIPTION
A detailed description of the method of describing soils is contained in BS 5930. The basic soils
are boulders, cobbles, gravels, sand, silt and clay. Often soils appear in mixtures and are referred
to composite types.
In accordance to BS 5930, a soil is of basic type sand or gravel (coarse soil), if after removal of
boulders and cobbles, over 65% of the material is in the sand and gravel range. A soil is of basic
type silt or clay (fine grained soil) when over 35% of the soil is in the silt and clay range.
Composite soils are named as described in the table 1. Mixtures containing over 50% boulders
and cobbles are referred to as very coarse soils. The descriptions may be of the form COBBLES
with finer material or gravelly SAND with occasional cobbly BOULDERS.
The firmness or strength of the soil in the field can be assessed by means of tests
shown on Table 2 below.
SOIL STABILIZATION
Soil stabilization is a general term for any mechanical, physical, chemical or combined method
of changing a natural soil to meet an engineering purpose. Improvements include increasing the
weight bearing capacities, tensile strength and overall performance of in-situ soils, sands and
other waste materials in order to strengthen road surfaces.
Mechanical stabilization
The oldest types of soil stabilization are mechanical in nature. Mechanical solutions involve
physically changing the property of the soil somehow, in order to affect its gradation, solidity
and other characteristics. Dynamic compaction is one of the major types of soil stabilization; in
this procedure a heavy weight is dropped repeatedly onto the ground at regular intervals to quite
literally pound out deformities and ensure a uniformly packed surface. Vibro compaction is
another technique that works on similar principles, though it relies on vibration rather than
deformation through kinetic force to achieve its goals.
The soil stabilized with cement is known as soil cement. The cementing action is believed to be
the result of chemical reactions of cement with siliceous soil during hydration reaction. The
important factors affecting the soil cement are nature of soil content, conditions of mixing,
compaction, curing and admixtures used.
I. Type of soil: cement stabilization may be applied in fine or granular soil, however
granular is preferable for cement stabilization.
II. Quantity of cement: a large amount of cement is needed for the stabilization.
III. Quantity of water: Adequate water is needed for the stabilization.
IV. Mixing, compaction and curing: Adequate mixing, compaction and curing is needed for
cement stabilization.
V. Admixtures: cement has some important admixtures itself which helps them to create a
proper bond. These admixtures play vital role incase of reaction between cement and
water.
I. It is widely available
II. Cost is relatively low
III. It is highly durable
IV. Soil cement is quite weather resistant and strong
V. Granular soils with sufficient fines are ideally suited for cement stabilization as it
requires least amount of cement.
VI. Soil cement reduces the swelling characteristics of the soil.
VII. It is commonly used for stabilizing sandy and other low plasticity soils. Cement interacts
with the silt and clay fractions and reduces their affinity for water.
Slaked in lime is very effective in treating heavy plastic clayey soils. Lime may be used alone or
in combination with cement, bitumen or fly ash. Sandy soils can also be stabilized with these
combinations. Lime has been mainly used for stabilizing the road bases and the subgrade.
I. Type of soil: lime stabilization is useful for stabilization of clayey soils but it is not
effective for sandy soils.
II. The amount of lime required for stabilization varies between 2 to 10% of the soil.
III. Ratio of fly ash to lime: The ratio of fly ash to lime generally varies in between 3 to 5.
The fly ash used is about 10 to 20% of the soil weight.
IV. Different type of lime: The quick lime is more effective but for safety and convenience to
handle the hydrated lime is generally used.
V. Soil becomes more workable
VI. Strength is generally improved.
VII. Lime stabilization increases the compressive strength sometimes as high as 60 times.
VIII. It is not effective for sandy soils
I. Lime is produced by burning of lime stone in kilns, so that it is harmful for environment.
II. It needs more cost to burnt limestone
III. It is not effective for sandy soils.
IV. There is limited percentage of amount of lime required about 2 to 10% of the soil.
The addition of bitumen binder to a soil improves its properties considerably. If the bitumen
lacks cohesion, the bitumen coats the soil particles, binds them together and supplies cohesion.
Bitumen being a waterproof material, the mixture becomes less prone to the adverse effect
caused by ingress of water. If bitumen binder sprayed on dry surface of low-cost road it prevents
dust and stops the entry of moisture into the road.
2.1 Introductions
Definition; ―A clay is an earthly mineral mass or an earthly fragment rock capable of forming
with water a plastic paste which retains the shape impartial to it after it is allowed to dry out and
which acquires the hardness of stone after burning‖.
Clays and clay minerals have been mined since the Stone Age; today they are among the most
important minerals used by the building and manufacturing industries. The term clay is applied
both to minerals having a particle size of less than 2 micrometers and to the family of minerals
that have similar chemical composition and common crystal structural characteristics.
Thus clays may be composed of mixtures of finer grained clay minerals and clay-sized crytals of
other minerals such as quartz, carbonate, and metal oxides. Clay and clay minerals are found
mainly on or near the surface of the earth and are predominantly made of Silica (SiO2) and
Alumina (Al2O3).
2.2.1 Erosion
The transport and deposit of clays and clay minerals produced by eroding older continental and
marine rocks and soils are important cycles that form sedimentary rocks. The ancient
sedimentary rock record is composed of 70% mudstone (contains approximately 50% clay –
sized fragments) and shale (may contain clay – sized particles), Blats etc. today sedimentary
Environments that contain mud cover about 60% of marine continental shelves and 40% of deep
ocean basin. Clearly clays are critical components of both ancient and modern
sedimentaryenvironments.
Weathering of rocks and soil is the primary way that clay and clay minerals form at the Earth‘s
surface today. The weathering process involves physical disintegration and chemical
decomposition that change original minerals to clay minerals. Weathering is uneven and many
stages of breakdown may be found in the same clay sample. The type of clay minerals found in
weathering rocks strongly control how the weathered rock behaves under various climate
conditions.
Kaolinite is found in most weathering zones and soil profiles. Montmorillonite are common in
the lower parts of the weathering profiles nearer rock, where chemistry exerts a strong control on
mineralogy. Complex – mixed day minerals (such as illite-smectites) are abundant in day
assemblages that develop from mica-beating precursor rocks.
The characteristics common to all clay minerals derive from their chemical composition, layered
structure and size.
Water absorption =
Some clay swells easily and may double in thickness when wet. The process of swelling is
reversible and it depends on the environment factors
When a little clay is added to water, slurry forms because the clay distributes itself evenly
throughout the water. This property of clay is used by the paint industry to disperse pigments
evenly throughout paint.
A mixture of a lot of clay and water (little) results on a mild that can be shaped and dried to form
a relatively rigid solid. This property s exploited in the building industry and ceramic industry to
produce various clay products.
ENGINEERING MATERIALS & CONCRETE TECHNOLOGY
Page 43
Most clay minerals have the ability to soap up ions from a solution and release the ions later
when conditions change.
The ability of clay mineral structures to exchange ions relates to their charged surface.
Ions can be attracted to the surface of a clay particle or taken up within the structure of these
minerals.
Clays are classified in two ways; on the basis of their mode of formation and on the basis of
dominant characteristics
Residual clays are those that are found at the place of their formation. They generally form a
cover over the rock from which they have been formed as a result of weathering processes. Such
clays are pure in their composition, which is related broadly to the parent rock. China day in
generally a residual type of clay.Residual type of clay. Residual clays are less common in their
occurrence.
Transported clays are the most common type of clay and are formed by deposition of the
disintegrated clayed and other materials produced by wind, water and ice from the erosion of
rocks from different places.
On the basis of the dominant characteristics, which actually related to their composition they are
of four types.
This is the purest type of clay containing a very high percentage of a clay mineral Kaolinite
(orKaolin) – Al2Si2O5(OH)4. It is considered high clay and is used for the manufacture of
porcelain ware and other special products e.g. fine – resisting cement, white Portland cement,
etc.
Thesecontain silica and Alumina in very high proportions. These clays are capable of
withstanding very high-temperatures without deformation of shapes given to them. They are
mainly used for the manufacture of refactory bricks, which are very important lining material in
high-= temperature metallurgical, mechanical and chemical operations.
c) Vitrifying clays
Theseclays are rich in fluxing compounds like Iron Oxide and carbonates of Calcium and
Magnesium. They are easily fusible, that is cannot withstand high temperatures.
On heating to high temperatures, (above 110000), the fluxes get softened and form glass – like
material that acts as a strong binding agent between the other clay particles. This results in the
formation of a smooth – surfaced clay product.
The vitrifying clays, also called hard-burning clays, for the above reason are specially used for
the manufacture of facing bricks, flooring tiles, sewer pipes and other similar ornament and
dense clay products.
These are low grade clays, quite rich on a variety of components, chief among which are Silica,
Alumina, Oxides of Iron, Lime and Magnesia and Organic matter. It is the mutual proportion of
these components that defines their suitability or otherwise for making good quality bricks for
building construction.
The brick clays are generally of transported group of clays. By virtue of their common
occurrence, these have been widely used for making of building bricks and ordinary load bearing
or partition tiles.
Clay products are those materials (products) that are made from clay... construction materials
such as bricks, tiles, refractory bricks, earthenware and stoneware are example of clay products.
The brick is the most commonly used building material, though tiles, refractory blocks, earth
ware and stoneware serve different construction purpose. Bricks are commonly used for
constructing walls, columns, roofs, paving floors and as aggregate for concrete work in
foundations under – floors etc.
Tiles are thin slab of brick earth burnt in a kiln. Tiles are thinner than bricks and have a greater
tendency to crack and warp in drying than ordinary bricks and are more liable to breakage.
Therefore, greater care is needed in their manufacture. They should be dried in the shade,burnt
and cooled in specially made kilns.
The differenttypes of tiles are distinguished on the basis of their use. The five major classes
include; roofing tile, wall tiles, flooring tiles drain tiles and glazed earthen ware.
Roofing tiles form the single most important and most commonly used class of tiles. They are
used as alternatives to corrugated and plain G.I sheets and timber as roofing material, especially
on slopping roofs.
i. Plain tiles: measures about 25cm x 15cm o 28cm and from 10mm to 17mm thick.
These may have a continuous projection at one end or two small projecting nibs.
These nibs should not be less than 2cm wide and 1 cm deep. Camber should be
between 5mm and 10mm for handmade tiles. The camber could be reduced for
machine made tiles.
Diagram missing.
ii. Pot tiles: they are semicircular in section and taper along the length. Diameter at larger
end is about 23cm and at the smaller end it is about 20cm. rows of these tiles are laid
with the concave side up. Then rows of same tiles with convex sides up are laid to
cover the adjoining edges of every pair of the previously laid tiles.
Diagram missing
iii. Allahabad tiles: these consist of two sets of tiles. The lower ones are flat tiles with
upturned sides. End widths reduce from 27cm to 23cm and the length is about 38cm,
the cover tile is half round in section and tapers from 16.5cm to 12cm in diameter.
Taper allows the tile in the next course to fit in. half round tiles are moulded on a
potter‘s wheel as a round tapering cylindrical tile. Two longitudinal cuts are given to
the cylinder while still to dry. With this it is easy to break it into two semicircular tiles
after burning.
Diagram missing.
iv. Mangalore tiles: these are very common. They are flat pattern tiles with suitable key
projection. About 16 tiles are required to cover one square meter of roof. The
arrangement of Mangalore tiles on a slopping roof is shown below.
Diagram missing.
v. Pan tiles: the tiles are curved in section. These are 33cm to 38cm long and 23cm to
28cm wide. Implements needed for its moulding are mould, a horse, a bow and strike.
Diagram missing
b) Flooring Tiles
These tiles are flat and usually square or rectangular in shape and can be made in any clour or
geometric shape. The tiles should give a ringing sound when struck with each other, should not
absorbed more than 24% water, by weight and should have maximum resistance to impact.
c) Wall tiles
These are similar to floor tiles except for their design and burning. They are burnt at a
comparatively low temperature, glazed and burnt again at still low temperatures. They can be
made in different designs and colours and be built to any size. They are used on face work, to
some extent on arches for architectural ceilings, etc.
d) Drain tiles
These tiles are usually long curved sections of various shapes and sizes such as semi- circular, a
segment of a circular or circle. They are generally used for draining wastewater. If employed for
carrying sewage, glazed tiles are used.
In case of floating tiles, warpage should not exceed 2% along the edges and 1.5% along the
diagonal.
In case of terracing (flat tiles), maximum warpage should not exceed in any direction by 1%
Water absorption test for roofing, flooring and terracing tiles is carried out as follows:
Take six tiles and dry them in an oven at a temperature between 1000c and 1100c, until they
attain a constant wright and then cool.
Weigh tem (W1) and immerse them completely in clean water at temperaturebetween 240c and
300c for 24 hours.
Remove each specimen, wipe off the surface water with a damp cloth and weigh the specimen
within 3 minutes after removing the specimen from water (W2)
c) General quality
They should be free from irregularities such as bend, cracks, trusts etc.
i. Preparation of clay
The selected clay is made free from any impurity such as grit, pebbles and the clay is ground into
powder in a crushing roller or molls and then thoroughly pugged. For manufacture of superior
tiles, the powder is mixed with a large quantity of water in a tank, stirred and the mixture is
allowed to settle. The heavier particles sink to the bottom and the fine ones are runoff into a
lower tank, where the water is evaporated, and leaving fine clay ready for mixing. To make the
tiles hard and impervious, a mixture of ground glass and pottery ware may be added in the
required quantities to the clay of the tiles.
The tiles are moulded using any of the three methods namely; wooden patterns, potter‘s wheel or
mechanical method. The method used as mainly determined by the shape and cross section of the
tile required.
Two days after moulding, tile is slightly beaten with a flat wooden mallet to correct the
irregularity in shape due to warping. The tiles are lifted up on the next day andedges and under
surface scrapped. They are then placed on edge and left to any for about 2 days under shade (to
prevent warping and cracking when they are ready for loading in the kiln).
As outlined in the introduction, bricks are the most popular construction clay products. Bricks do
not require dressing like stones and the art of laying bricks is so simple that the brick work can
be carried out with the help of unskilled labourers. Also in places where stores are not easily
available, but there is plenty of clay suitable for manufacture of bricks can replace the functions
of the stones.
A good earth should be such that if can easily be moulded and dried without cracking and
warping. A good brick earth should be composed of Alumina, Silica and Silt (majorconstituents),
and iron oxide, magnetism oxide (magnesia), lime and sodium potash (minor constituents). All
the constituents should be in proper proportions to produce a brick with good quantities such as
hardness, controlled shrinkage, lack of cracks, controlled warping and dying, durability
resistance to heat, good binding properties, good colour, etc.
Homogenous
These are bricks where appearance and high strength are not importance. Common bricks are
used in inferior and temporary buildings, for internal walls where the bricks are generally hidden
from view, and may be used as aggregates (when crushed) for making concrete to be used in
foundation floors, etc.
b) Facing bricks
Facing bricks are used for decoration. These bricks are used in the exposed face of masonary
without any further surface protection.
The use of such bricks is economical where external plastering or rendering have to be
frequently renewed due to corrosive atmosphere and also for high – raise buildings.
These are also referred to as heavy duty bricks. They are characterized by high compressive
strength, low water absorption, high durability and high bulk density. They should be free from
cracks and other flaws.
These heavy –duty may have compressive strength as high as 44N/mm2 and water absorption as
low as 5% with the least efflorescence.
Such bricks are required for masonary in heavy engineering world such as bridge structures,
multi-storeyed buildings, and industrial foundations and in situations where construction has to
remain in contact with water.
Properties of bricks
Manufacture of bricks
i) Preparation of clay.
The top layer of soil (about 200mm depth) is taken out and throw – away and the soil below is
dug out and cleared off shore, pebbles, vegetable matter etc. all lumps are broken to powder
form.
The earth is then spread out to a depth of 600 to 1200mm and left to atmospheric action; this
process is known as weathering. This process can extend from a few weeks to some months and
imparts plasticity and strength to clay. It is at this stage that the earth soil is blended with
different types of earths such as sandy or calcareous clays in appropriate proportions with little
quantities of cocked, ash etc. to develop the essential qualities needed for moulding, drying and
burning of bricks.
The whole mass is mixed uniformly and proportionate quantity of water added. The earth is
covered up with cloth or mats.
The tempering process, which consists in kneading the earth under feet of men or cattle or use of
a pug mill to make it stiff and plastic, follows. Water is added from time to time and tempering
continued till a homogenous mass of earth is obtained.
After the earth is prepared, the, moulding of bricks is carried out either by hand or by machine.
Hand moulding usually adopted is either ground or table moulding. Amachine can be performed
either by the plastic method or the dry process method.
a) Natural drying; also referred to as hack drying consists of arrangement the wet bricks
in rows on their edges on slightly raised ground called hacks. A little space for
circulation of air is kept for each brick. It should be ensured that no sudden drying
ENGINEERING MATERIALS & CONCRETE TECHNOLOGY
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occurs, caused by direct sun and wind. A portable cover is also provided to protect
the bricks from rain. In places where temperature variations are too much, temporary
sheds are reacted for drying purposes
The bricks produced (air and sun dried) are adequately strong for construction of simple
structures.
b) Artificial drying; this method is used when bricks are required on large scale and at a
rapid rate. The heating of the brick is carried out in special driers such as tunnels or
chambers which receive heat from special furnaces, built for the purposes not flue
gases from the cooling chambers of a kiln and waste steam from the engines of
driving machinery.
iv. Burning /firing of bricks
Bricks after being moulded and dried are burnt on the kilns. The purpose of burning its o imparts
hardness and strength to the bricks and to increase the density of the bricks so that they will
absorb less quantity of water. The Kiln used may be of the clamp or open type, intermittent type
or continuous type, each with its pros and cons.
This is the commonest method employed for burning bricks (ordinary bricks).
The method of burning is suitable for burning only ordinary bricks and it is employed in rural
areas where transport charges of bricks from urban areas are high. Furth more, as the number of
bricks required for the construction of an ordinary building is small; it is not felt necessary to set
up bigger Kilns, which entail a huge expenditure. Clamp or Open Kilns are temporary structures
The size of the clamp depends on the number of bricks required. In a typical clamp, a slopping
ground is prepared in a trapezoidal shape, with the narrow end excavated below the ground and
the wider end is raised by filling. The slope angle is about 150.
In a clamp, fuel and bricks are arranged in alternate layers. On the sides and on top of the clamp,
some protection is provided by a coating of earth. The air –dried – bricks are arranged in layers
Advantages
bricksproduced are tough and strong (due to gradual burning and cooling )
Disadvantages
The process is very slow; therefore time required for burning is very long
The quality of bricks produced is not uniform (since the burning is not uniform)
Intermittent Kilns
Intermittent Kilns are permanent clamps and can be put to use for burning bricks, here the
burning is not continuous. Intermittent Kilns are made rectangular or circular in shape and may
be of ―upward drought‖ or ―downward drought‖ type. Brunt bricks from these Kilns can be made
only after a definite interval of time once they have been fired. (Brick supply is intermittent.)
Continuous Kilns
Continuous Kilns are those types from which it is possible the supply of bricks almost
continuously. This is because they consist of a number of chambers. Working in these chambers
is so arranged that at any given time if one chamber is being loaded with dried bricks, another
chamber may be in burning process and another in the un-loading process.
The specimen brick is first weighed dry (after drying in an oven between 100 and 1100c) - W1
Water absorption =
Soluble salts, if present in the bricks, cause efflorescence on the surface of the bricks
Procedure
Immerse the brick to be tested in water for 24hours and then taken out and allowed to dry in a
shade.
The absence of grey or white deposits on its surface indicates absence of soluble salts
If white deposits cover about 10% surface, theefflorescence is said to be slight and it is
considered moderate when the white deposits cover about 50% of the surface. Greater than 50%,
the efflorescence becomes heavy and is considered serous.
A good structure should be homogenous, compact and free from any deposits e.g. lumps, holds
etc.
The test is performed by striking two specimen bricks with one another; the bricks should not
break and a clear ringing sound should be produced
In this test, specimen brick should be closely inspected. It should be of standard size and its
shape should be truly rectangular with sharp edges
Twenty bricks of standard size are randomly selected and stacked length – wise, along the width
and along the height.
For good quality bricks, the results should be within the following permissible limits length;
3920mm; width 1740 to 1860mm; height: 1740 to 1860mm for bricks of standard size (190 X 90
X 90mm)
The frog of the brick is filled with a 1:3 mortar mix and the brick is stored under damp jute bags
for 24 hours, followed by immersion in clean water for three days.
The specimen is then paled between the plates of the compression testing machine
The load is applied axially at a uniform rate of 14N/mm2. The maximum lad at which the
specimen fails is noted for determination of the compressive strength of brick given by;
Compressive strength =
The crushing or compressive strength of common building bricks should not be less than
3.5N/mm2. Bricks of high quality do not have strength > 14N/mm2.
i. First class bricks: these bricks are of standard shape size. They are burnt in kilns. They
fulfill all desirable properties of bricks.
ii. Second class bricks: these bricks are ground moulded and burnt in kilns. The edges may
not be sharp anduniform. The surface may be somewhat rough. Such bricks are
commonly used for the construction of walls which are going to be plastered.
iii. Third class bricks: these are the over burnt bricks. They are dark in colour. The shape is
irregular. They are used as aggregates for concrete in foundations, floor and roads.
Uses of bricks
i. As building blocks.
ii. For lining of ovens, furnaces and chimneys
iii. For protecting steel columns from fire.
iv. As aggregates in providing water proofing to R.C.C roofs.
v. For pavers for footpaths and cycle tracks
vi. For lining sewer lines
3.0 Timbers
Introduction
Timber refers to wood used for construction works, in fact the word timber is derived from an
old English word ‗Timbrian‘ which means ‗to build‘. A tree that yields good wood for
construction is called ‗standing Timber‘. After felling a tree, its branches are cut and its stem is
roughly converted into pieces of suitable length, so that it can be transported to timber yard. This
form of timber is known as rough timber. By sawing , rough timber is converted into various
commercial sizes like planks, battens, posts, beams etc. such form of timber is known as
converted timber. Timber was used as building material even by primitive man. Many ancient
temples, places and bridges built with timber can be seen even today.
Classification of timber
Various bases are considered for the classification of timbers. The following are the important
basis
i. Mode of growth
ii. Modulus of elasticity
iii. Durability
iv. Grading
v. Availability
I. Classification based on mode of growth
a. Exogenous
b. Endogenous
(a) Exogenous trees: These trees grow outward by adding distinct consecutive ring every
year.
1.Coniferous
2.Deciduous
Coniferous tree are having cone shaped leaves and fruits. The leaves do not fall till new ones
are grown. They yield soft wood.
Deciduous trees are having broad leaves. These leaves fall in autumn and new ones appear in
springs. They yield hard wood and hence they are commonly used in building construction
The classification as soft wood and hard wood has commercial importance. The difference
between soft wood and hard wood is given below.
1.In soft wood annual rings are seen distinctly whereas in hard wood they are indistinct
2.The colour of soft wood is light whereas the color of hard wood is dark.
3.Soft woods have lesser strength in compression and shear compared to hard woods
4.Soft woods are light and hard woods are heavy.
5.Fire resistance of soft wood is poor compared to that of hard wood.
6.The structure of soft wood is reinous while structure of hard wood is close grained
The cross section of an exogenous tree is as shown in the fig. 1.9. The following components are
not visible to the naked eye
Group A: E = 12.5KN/mm2
III. Classification based on durability: Durability tests are conducted by the forest research
establishment. They bury test specimen of size 600 x 50 x 50mm in the ground to half
their length and observe their conditions regularly over several years. Then timbers are
classified as: high durability: average life between 5 to 10 years
IV. Classification based on grading: IS 883-1970 classifies the structural timber into their
grades select, grade-1 and grade-II respectively. The classification is based on
permissible stresses defects etc.
V. Classification based on availability: forest departments classify timbers based on the
availability as;
PROPERTIES OF TIMBER
Warping: Good timber does not warp under changing environmental conditions.
Abrasion: Good timber does not deteriorate due to wear. This property should be looked into, if
timber is to be used for flooring.
Strength: Timber should have high strength in bending, shear and direct compression.
Workability: Timber should be easily workable. It should not clog the saw.
Durability: Good timber is one which is capable of resisting the action of fungi and insects
attack
Defects: Good timber is free from defects like dead knots, shakes and cracks.
CONVERSION OF TIMBER:
The process by which timber is cut and sawn into suitable sections is known as the conversion.
Following important facts in connection with the conversion of timber are to be
remembered:
ORDINARY SAWING
Fig. 9-4 shows ordinary sawing or bastard sawing or flat sawing or slab sawing. The saw cuts are
tangential to the annual rings and right through the cross-section of timber piece. The log is
moved forward and backward on the platform of a sawing mill. Thus the parallel cuts are made
throughout the length of the log and parallel slices of planks are obtained.
This is a very easy and quick method of sawing and it is widely adopted in our country. It is also
most economical method and wastage of useful timber is minimum. However the planks
obtained by this method are liable to warp and twist as a result of unequal shrinkage. The outer
portion is of sap wood and it shrinks more.
QUARTER SAWING
The saw cuts are at right angles to each other. It may produce fine figure wood when adopted in
case of timber having no distinct medullary rays. In this method, there is a tendency for the
timber to bend in a transverse direction.
TANGENTIAL SAWING
Fig. 9-6 shows tangential sawing or plain sawing or flat grained sawing. The saw cuts are
tangential to the annual rings and they meet each other at right angles. This method is adopted
when the annual rings are very distinct and the medullary rays are not clearly defined.
The planks obtained by this sawing warp too much because the sections are weak as the
medullary rays which impart strength to the longitudinal fibres are cut. The timber obtained by
this method is unsuitable for flooring and it cannot be polished evenly.
During conversion, there will be loss of timber due to sawing and it may extend up to 40 per cent
in reduction of weight of log.
SEASONING OF TIMBER
Timber seasoning refers to the controlled drying of converted timber by natural or artificial
means.
a. To ensure that shrinkage takes place before timber is used. (To avoid distortion of
finished work).
b. To ensure that the moisture content of timber is below the dry rot safety line of
20%
c. To increase the strength of timber
d. To enable finishes like painting, varnishing, gluing, preservation etc.
e. To reduce timber weight for easy transportation
f. To make timber easily workable.
g. To reduce the risk of insect/fungal attack on timber.
A. Air/natural seasoning.
This is the method of seasoning, where timber is stacked in open sided sheds. Which
facilitate free air circulation within timber and afford it protection from sun and rain. When
choosing the site, the following factors should be born in mine.
(i) The site should be open, well drained and concreted to prevent vegetative
growth. Where cleanliness ought to be observed.
(ii) Brick piers should be constructed to keep the stack off the ground for the
good air circulation.
(iii)Stack the boards horizontally from the largest to the smallest, and once
piece separated by stickers at 25mm from each other to prevent distortion.
(iv) Pilling sticks (stickers) should be introduced between each layer at
approximately 600mm and should be of the same type of timber as that
being seasoned to avoid staining.
NB Hardwood boards converted using slab sawing should be stacked as they were converted
Conditions that affect the drying time of timber when air seasoned.
This is a method of drying timber in built up chambers, through which air of controlled humidity
and is circulated by powerful electric fans.
It is therefore a mechanized process commonly used for rapid seasoning timber especially for
internal use. This method can also be used in conjunction with air seasoning to achieve the
required moisture content.
This is a brick or concrete building to which the timber is packed similar to air seasoning.
Timber remains stationery during the seasoning process while the conditions are adjusted to the
correct levels as the drying process progresses. Inside the kiln, warm air is circulated by means
of fans, while steam or water vapour jets control humidity.
In this method, timber is dried out to required moisture content as tests are periodically carried
out to check on the progress of the drying process, which should be controlled to avoid impairing
timber by too rapid drying.
A progressive kiln is a drying tunnel where timber is packed and moved in trunks / trolleys
gradually from warm and humid to hot and dry conditions. They are normally used in situations
where there is need for constant supply of timber of the same species.
The drying schedules are such that when high steam is introduced, lower the heat. Reduced
steam, increase heat.
(a) Boiling. In this method timber is immersed in water and then water is boiled for 3 to 4
hours. Then it is dried slowly. Instead of boiling water hot steam may be circulated on
timber. The process of seasoning is fast, but costly.
(b) Chemical seasoning. In this method, the timber is immersed in a solution of suitable salt.
Then the timber is dried in a kiln. The preliminary treatment by chemical seasoning
ensures uniform seasoning of outer and inner parts of timber.
(c) Electrical seasoning. In this method high frequency alternate electric current is passed
through timber. Resistance to electric current is low when moisture content in timber is
high. As moisture content reduces the resistance reduces. Measure of resistance can be
used to stop seasoning at appropriate level.
However it is costly process. This technique has been tried in some plywood industries but not in
seasoning of timber on mass scale.
DEFECTS IN TIMBER
Various defects which are likely to occur in timber may be grouped into the following three.
(a). knots: when a tree grows, many of its branches fall and the stump of these branches in
the trunk is covered. In the sawn pieces of timber the stumps of fallen branches appear as
knots. Knots are dark and hard pieces. Grains are distorted in this portion. Figure 1.9 shows
some varieties of knots. If the knots are intact with surrounding wood, it is called live knot. If
it is not held firmly it is dead knot.
(b) Shakes. The shakes are cracks in the timber which appear due to excessive heat, frost or
twisting due to wind during the growth of a tree. Spending upon the shape and the
positions shakes can be classified as star shake, ring shakes and heart shakes (ref.
fig.1.10)
(d) Upsets: figure 1.12 shows a typical upset in a timber. This type of defects is due to
excessive compression in the tree when it was young. Upset is an injury by crushing. This
is also known as rupture.
(ii) Defects due to defective seasoning and conversion. If seasoning is not uniform, the
converted timber may warp and twist in various directions. Sometimes honey
combining and even cracks appear. This type of defects is more susceptible in case of
kiln seasoning. In the process of converting timber to commercial sizes and shapes
the following types of defects are likely to arise, chip marks, torn grain etc.
(iii) Defects due to fungi and insects attack. Fungi are minute microscopic plant
organism. They grow in wood if moisture content is more than 20oc and exposed to
air. Due to fungi attack rotting of wood, takes place. Wood becomes weak and stains
appear on it. Beetles, marine borers and termites (whit ants) are the insects which eat
wood and weaken the timber. Some woods like teak have chemicals in their
compositions and resist such attacks. Other woods are to be protected by chemical
treatment.
Dry rot; is the decomposition of felled timber by the action of various fungi which feed up on
the wood and reduces it to powdery condition. This disease highly destroys timber but charring,
painting or varnishing unseasoned timber can also cause dry rot. Dry can also be detected in
timber by scratching or tapping timber from one side and listening from one side if the noise is
heard easily then the timber internal decay.
Prevention of dry rot; These can be done by keeping timber in dry state with adequate
ventilation, reliable DPC layer and avoidance of any leakage to the timber.
Keep the timber at maximum moisture content of 20% to avoid the development of any fungi.
If dry rot is detected in timber, remove the affected one immediately and burn it off.
Wet rot; It is the decomposition of timber caused by dampness and moisture and by alternate
wetting and drying, these type of decay is not caused by fungal attack. It is commonly found in
living trees, the attack takes place through wounds in the bark by the access of water.
Prevention of wet rot; By using well-seasoned wood for both exterior and underground work.
Wood should be protected from moisture by tarring or painting
PRESERVATION OF TIMBER
Is the art of treating the timber with some chemicals so as to increase its life span. The major
aims of preserving timber are;
To protect the timber structure from the attack of destroying agencies such as fungi,
insects etc.
To lengthen the life of timber structures.
To make the timber structures durable.
Timber is to be seasoned well before application of preservatives. The following are the widely
used preservatives.
1. Tar oils
These are derived from coal and dark brown or black in colour. They are fairly permanent,
cheap, effective and easy to apply. They are however have a strong odor and are flammable.
They are used mainly for external use and the timber treated using tar oils will not accept finish
such as paint and varnish.
These are toxic chemicals which are mixed with a spirit that evaporates after the preservative has
been applied to the timber. They are the most expensive types of preservatives but considered to
be superior because of their excellent penetration properties.
1. Brush applications,
2. Dipping,
3. Open tank immersion,
4. Pressure application.
1. Brush Application;
In this method, timber is given one or two coats of the preservative with the help of a brush. This
is used for painting the ends of beams or base of poles and posts that go to the ground with coal
tar. The method is quite cheap. At the same time, it is not very effective.
2. Dipping Application;
The timber part to be treated is made to dip in the preservative and kept immersed in it for
various periods from a few hours to few days. It is used when organic preservative solvents are
to be applied.
In this way, the timber may actually suck a lot of preservatives and ensure complete penetration.
Softwoods (confiners) receive this type of treatment in a remarkable manner because their cells
are more permeable. The treatment has the disadvantage that it increases the weight of the treated
timber considerably.
The Full-Cell Process. The timber is placed in a large steel cylinder acting as a pressure vessel.
Vacuum is created and maintained for about one hour or more. After this, coal tar creosote oil or
any other suitable preservative, preheated to a required temperature, is forced into the cylinder
under sufficient pressure. This is continued till the required quantity of preservative has been
introduced into the timber. Thereafter, the pressure is reduced, and after giving some vacuum,
timber is taken out.
Empty cell method; no vacuum is created in the beginning. Instead, timber placed in the
pressure vessel is subjected to initial pressure while preservative is being introduced into the
cylinder. Once the vessel is full of preservative, full pressure is applied which forces the
preservative from the tank into the timber. After this, the pressure is released. This causes the air
compressed in the cells of timber to come out along with any excessive preservative.
The main advantage of pressure processes (of one type or another) is that they ensure a proper
and deeper penetration of preservative into the timber in a controlled manner.
Even those timbers which may not absorb preservatives in the open-tank process can be filled
with preservatives by this method.
Charring. It is a common method used for preserving timber poles and posts that are to be dug
into the ground. The outer part of the lower ends is charred (incompletely burnt) before insertion
into the ground. The charcoal layer so formed is an easy safeguard against attacks by fungi or
termite (as these organisms do not find any food in charcoal).
Uses of timber
Introduction
Stone is naturally available building which has been used from the early age of civilization. It is
available in the form of rocks, which is cut to required size and shape and used as a building
block.
A rock is commonly defined as a hard mass of mineral having as a rule, no definite external form
(shape) or chemical composition, but a mixture of two or more minerals. A mineral is a
substance, which is formed by the natural organic process and possesses a definite chemical
composition and molecular structure.
Building stones are those types of stones that possess such properties, which make them suitable
for building construction.
Type of stones
Stones used for civil engineering may be classified in the following three ways
- Geological
- Physical
- Chemical
Geological classification
Based on their origin of formation stones are classified into three main groups – igneous,
sedimentary and metamorphic rocks
(i) Igneous rocks. These rocks are formed by cooling and solidifying of the rock masses
from their molten magmatic condition of the material of the earth. Generally igneous
rocks are strong and durable. Granite, trap and basalt are the rocks belonging to this
category; granites are formed by slow cooling of the lava under thick cover on the
Physical classification
- Stratified rocks
- Unstratified rocks
- Foliated rocks
(i) Stratified rocks. These are rocks having layered structure. They possess planes of
stratification or cleavage. They can be easily split along these planes. Sand stones,
lime stones slate etc. are the examples of this class of stones
(ii) Unstratified rocks. These rocks are not stratified. They possess crystalline and
compact grains. They cannot be split in to thin slab. Granite, trap, marble etc. are the
examples of this type of rocks.
Chemical classification
On the basis of their chemical composition engineers prefer to classify rocks as:
- Silicious rocks
- Argillaceous rocks and
- Calcareous rocks.
(i) Silicious rocks. The main content of these rocks is silica. They are hard and durable
(ii) Argillaceous rocks. The main constituent of these rocks is argil i.e. clay. These stones
are hard and durable but they are brittle. They cannot withstand shock. Slates and
laterites are examples of this type of rocks
(iii) Calcareous rocks. The main constituent of these rocks is calcium carbonate.
Limestone is a calcareous rock of sedimentary origin while marble is a calcareous
rock of metamorphic origin.
PROPERTIES OF STONES
The following are the engineering and physical properties of the stones that should be looked
into before selecting them for engineering works:
1. Structure. The structure of the stone may be stratified (layered) or unstratified. Structured
stones should be easily dressed and suitable for super structure. Unstratified stones are hard and
difficult to dress. They are preferred for the foundation works.
2. Texture. Fine grained stones with homogeneous distribution look attractive and hence they
are used for carving. Such stones are usually strong and durable.
3. Density. Denser stones are stronger. Light weight stones are weak. Hence stones with specific
gravity less than 2.4 are considered unsuitable for buildings.
Slate 70 to 210
Marble 72
Sand stone 65
6. Hardness. It is an important property to be considered when stone is used for flooring and
pavement. For road works coefficient of hardness should be at least 17. For building works
stones with coefficient of hardness less than 14 should not be used.
8. Porosity and absorption. All stones have pores and hence absorb water. The reaction of
water with stone causes disintegration. Absorption test is specified as percentage of water
absorbed by the stone when it is immersed under water for 24 hours. For a good stone it should
be as small as possible and in no case more than 5.
9. Weathering. Rain and wind cause loss of good appearance of stones. Hence stones with good
weather resistance should be used for face works.
10. Toughness. The resistance to impact is called toughness. It is determined by impact test.
Stones with toughness index more than 19 are preferred for road works. Toughness index 13 to
19 is considered as medium tough and stones with toughness index less than 13 are poor stones.
11. Resistance to fire. Sand stones resist fire better. Argillaceous materials, though poor in
strength, are good in resisting fire.
12. Ease in dressing. Cost of dressing contributes to cost of stone masonry to a great extent.
Dressing is easy in stones with lesser strength. Hence an engineer should look into sufficient
strength rather than high strength while selecting stones for building works.
13. Seasoning. The stones obtained from quarry contain moisture in the pores. The strength of
the stone improves if this moisture is removed before using the stone. The process of removing
ENGINEERING MATERIALS & CONCRETE TECHNOLOGY
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moisture from pores is called seasoning. The best way of seasoning is to allow it to the action of
nature for 6 to 12 months. This is very much required in the case of laterite stones.
TESTS ON STONES:
To ascertain the required properties of stones, the following tests can be conducted:
Just like a sponge, porous rocks have the ability to absorb water and other liquids. Water-
absorbing rocks are formed from minerals that can hold water in their crystal structure or
between grain boundaries. Such water absorption is often accompanied by a change in the
crystal dimension that manifests itself as a swelling of the rock. These rocks, including
pumice and sandstone, increase in weight and size as they take in water. For the water
absorption test, the specimens are dried in an oven for a specified time and temperature and
then placed in a desiccators to cool. Immediately upon cooling the specimens are weighed.
The material is then emerged in water at agreed upon conditions, often 23°C for 24 hours or
This test is carried out on stones which are used as aggregates for road construction.
The test result indicate the suitability of stones against the grinding action under traffic.
The resistance of stones to impact is found by conducting tests in impacting testing machine .
This test is normally carried out on sand stones to check the presence of calcium carbonate,
which weakens the weather resisting quality. In this test, a sample of stone weighing about 50
to 100 gm is taken and kept in a solution of one per cent hydrochloric acid for seven days.
The solution is agitated at intervals. A good building stone maintains its sharp edges and
keeps its surface intact. If edges are broken and powder is formed on the surface, it indicates
the presence of calcium carbonate. Such stones will have poor weather resistance.
(i) Granite: Granites are intrusive igneous rocks. Their colour varies from light gray to pink.
The only natural stones harder than granite are diamonds, rubies, and sapphires. Therefore,
choose granite when permanence, enduring color and texture, and complete freedom from
deterioration and maintenance are prime requirements. Granite is highly heat, scratch and
stain resistant, and is commonly used to face commercial and institutional buildings and
ENGINEERING MATERIALS & CONCRETE TECHNOLOGY
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monuments. Commercially, the term ‗granite‘ includes a range of other types of non-granite
dimension stone including any feldspathic crystalline rocks or other igneous or metamorphic
rocks which possess qualities similar to granite‘s grainy, interlocking texture. Many
variations of granite appear on the commercial market with white, gray, pink, and red being
the most common primary colors.
The structure is crystalline, fine to coarse grained. They take polish well. They are hard
durable. The compressive strength is 100 to 250 N/mm2. Specific gravity: 2.64 and absorption
2
less than 1%.Crushing strength: 110 to 140 MN/m . Colour depends upon that of
feldspar and may be brown/ grey/ green or pink. Scientifically, an intrusive (plutonic) similar
stones such as gabbro, diabase, anorthosite, sodalite, gneiss, and basalt are sometimes
sold as ―granite‖ commercially.
They are used primarily for bridge piers, river walls, and for dams. They are used as kerbs
and pedestals. The use of granite for monumental and institutional buildings is common.
Polished granites are used as table tops, cladding for columns and wall. They are used as
coarse aggregates in concrete.
Gabbro: It is a dark-colored (mafic) intrusive rock that consists of dark grey feldspar and
black to dark green minerals such as amphibole and pyroxene.
To a geologist, the term ―black granite‖ would be an oxymoron, since by definition granite
must be light colored.
(ii) Basalt and Trap: These are extrusive igneous rocks. The structure is medium to fine
grained and compact. Their colour varies from dark gray to black. Fractures and joints are
(iv) Slate: These are metamorphic rocks. They are composed of quartz, mica and clay
minerals. While slate is primarily comprised of quartz and either muscovite or illite,
quantities of biotite, chlorite, hematite, and pyrite are also commonly present. Less
frequently, apatite, graphite, kaolin, magnetite, tourmaline, and zircon can be constituents, as
well. The structure is fine grained. They split along the planes of original bedding easily. The
colour varies from dark gray, greenish gray, purple gray to black. The specific gravity is 2.6
to 2.7. Compressive strength varies from 100 to 200 N/mm2. They are used as roofing tiles,
slabs, pavements etc. Slate is naturally found in an array of colors. The most common include
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black, gray, blue-gray, and mottled varieties. When iron compounds are present in the
formation, slate can take on hues of brick red, deep purple, or one of many shades of green.
(v) Laterite: It is a alteration product of a rock. It is having porous and sponges structure. It
contains high percentage of iron oxide. Its colour may be brownish, red, yellow, brown and
grey. Its specific gravity is 1.85 and compressive strength varies from 1.9 to 2.3 N/mm2. It
can be easily quarried in blocks. With seasoning it gains strength. When used as building
stone, its outer surface should be plastered.
(vi) Marble: This is a metamorphic rock. It can take good polish. It is available in different
pleasing colours like white and pink. Its specific gravity is 2.65 and compressive strength is
70–75 N/ mm2. It is used for facing and ornamental works. It is used for columns, flooring,
steps etc. Marble formed from very pure limestone is white, but the presence of other
minerals, as well as clay, silt and sand, can give it richly varied coloration. A wide variety of
marbles exist on the market, both foreign and domestic, and these can be drastically different
in density, hardness, porosity, and aesthetics.
(vii) Gneiss: It is a metamorphic rock. It is having fine to coarse grains. Alternative dark and
white bands are common. Light grey, pink, purple, greenish gray and dark grey coloured
varieties are available. These stones are not preferred because of deleterious constituents
present in it. They may be used in minor constructions. However hard varieties may be used
for buildings. The specific gravity varies from 2.5 to 3.0 and crushing strength varies from 50
to 200 N/mm2.
(viii) Quartzite: Quartzites are metamorphic rocks. The structure is fine to coarse grained
and often granular and branded. They are available in different colours like white, gray,
yellowish. Quartz is the chief constituent with feldspar and mica in small quantities. The
specific gravity varies from 2.55 to 2.65. Crushing strength varies from 50 to 300 N/mm2.
They are used as building blocks and slabs. They are also used as aggregates for concrete.
(i) Stone masonry is used for the construction of foundations, walls, columns and arches.
(iii) Stone slabs are used as damp proof courses, lintels and even as roofing materials.
(iv) Stones with good appearance are used for the face works of buildings. Polished marbles and
granite are commonly used for face works.
(v) Stones are used for paving of roads, footpaths and open spaces round the buildings.
(vi) Stones are also used in the constructions of piers and abutments of bridges, dams and
retaining walls.
(vii) Crushed stones with graved are used to provide base course for roads. When mixed with
tar they form finishing coat.
Aggregates are inert materials mixed with cement in the preparation of mortar or concrete.
However the aggregates may not completely be inert as in some cases their chemical
compositions may affect the properties of concrete in both its plastic and hardened states.
I. To improve both the volume stability and durability of the resulting concrete.
II. To reduce the cost of concrete. Most aggregates are natural materials which require only
extraction, washing and grading prior to transport to site.
III. Correctly graded aggregates produce workable yet cohesive concrete.
IV. To reduce the heat of hydration of concrete since they are normally chemically inert and
act as a heat sink for hydrating cement.
V. To reduce the shrinkage of concrete since most aggregates are not affected by water and
restrain shrinkage of the hydration cement.
VI. To control the surface hardness. Most aggregates have a better abrasion resistance the
hydrated cement but where heavy abrasion is anticipated, hard, high strength aggregates
such as granite or carborundum can be incorporated.
VII. For colour or light reflecting properties. Aggregates can be exposed for their visual
properties.
VIII. To control density of the concrete. Some light weight aggregates have densities below
5000kg/m3 while others have solid densities over 7000kg/m3. In general natural
aggregates have densities of 2600kg/m3 are widely used.
IX. To control fire. Light weight concretes are best in fire control because they transmit heat
most slowly than dense concrete.
Aggregate classification;
Aggregates are classified based on so many considerations, but here we are going to discuss
about their size, shape, unit weight and sources classifications in detail. An aggregate which has
substantial amounts of both fine and coarse aggregate is termed as an all-in aggregate.
Clay <0.002
Coarse Aggregate
These are the aggregates which have sizes more than 4.75 mm. In laboratories they are separated
as the aggregates which are retained on the BIS test sieve no. 480. Generally, broken stones are
used as the coarse aggregates.
Boulders >256mm
Size Use
50 to 75mm Roadwork
Cyclopean Aggregates
Rounded Aggregate
The rounded aggregates are completely shaped by attrition and available in the form of seashore
gravel. Rounded aggregates result the minimum percentage of voids (32 – 33%) hence gives
more workability. They require lesser amount of water-cement ratio. They are not considered for
high strength concrete because of poor interlocking behavior and weak bond strength.
Irregular Aggregates
The irregular or partly rounded aggregates are partly shaped by attrition and these are available
in the form of pit sands and gravel. Irregular aggregates may result 35- 37% of voids. These will
give lesser workability when compared to rounded aggregates. The bond strength is slightly
higher than rounded aggregates but not as required for high strength concrete.
Flaky Aggregates
When the aggregate thickness is small when compared with width and length of that aggregate it
is said to be flaky aggregate. Or in the other, when the least dimension of aggregate is less than
the 60% of its mean dimension then it is said to be flaky aggregate.
Lightweight concrete contains aggregate that is natural or synthetic which weighs less than 1100
kg/m3. The lightweight is due to the cellular or high internal porous microstructure, which gives
this type of aggregate a low bulk specific gravity. The most important aspect of lightweight
aggregate is the porosity. They have high absorption values, which require a modified approach
to concrete proportioning. For instance, slump loss in lightweight concrete due to absorption can
be an acute problem, which can be alleviated by prewetting (but not saturating) the aggregate
before batching.
This is composed of particles of high porosity resulting in low bulk density. The use of
lightweight aggregates reduces the dead weight of a structure, allowing the use of smaller
supporting members and foundations at reduced cost. It also gives improved thermal insulation.
Examples are; Slag, slate, pumice, sawdust and wood fibre, clinker and other light stones.
These are mainly used for the special purpose of screening radioactivity e.g. in nuclear plants.
Suitable aggregates are those with specific gravity greater than 4.0. These include certain
minerals like Hematite, barite magnetite, steel and iron punchings.
1. Natural aggregate: Native deposits with no change in their natural state other than
washing, crushing & grading. (Sand, gravel, crush stone).
2. Artificial aggregates: They are obtained either as a by-product or by a special
manufacturing process such as heating. (Blast furnace slag, expanded perlite)
SAMPLING
A test in the laboratory is carried out on the samples. So, certain precautions in obtaining a
sample must be taken to obtain ―representative sample‖. The main sample is made up of portions
drawn from different points.
1) Quartering:
2) Splitting:
Use the ―sample splitter‖ to divide the aggregate sample into two. Sample splitter is a box with
an even of chutes alternately discharging to two sides. The width of each chute should be greater
than 1.5 times the size of the largest aggregate size.
5.1 CEMENT
Cement is a commonly used binding material in the construction industry. The cement is
obtained by burning a mixture of calcareous (calcium) and argillaceous (clay) material at a very
high temperature and then grinding the clinker so produced to a fine powder. Today cement finds
extensive use in all types of construction works; in structures where high strength is required e.g.
bridge piers, light houses, lofty towers, and large structures such as bridges, silos, chimneys. And
also in structures exposed to the action of water, e.g. reservoirs, dams, dock yards etc. Cement
mortar, concrete, reinforced brick work, artificial stones, plastering, pointing and partition walls
are routinely used in buildings.
Cements used in construction industry may be classified as hydraulic and non-hydraulic. The
latter does not set and harden in water such as non-hydraulic lime or which are unstable in water,
e g. Plaster of Paris. The hydraulic cement set and hardens in water and gives a product which is
stable. Portland cement is one such.
The three constituents of hydraulic cements are lime, silica and alumina. In addition, most
Cements contain small proportions of iron oxide, magnesia, sulphur trioxide and alkalis.
8. Alkaline:
The various constituents combine in burning and form cement clinker. The compounds formed
in the burning process have the properties of setting and hardening in the presence of water.
They are known as Bogue compounds after the name of Bogue who identified them. Le-
Chatelier and Tornebohm have referred these compounds as Alite (C3S), Belite (C2S), Celite
(C3A) and Felite (C4AF). The following Bogue compounds are formed during clinkering process.
S.NO COMPOUND FORMULA NAME SYMBOL
1. Tricalcium silicate 3CaO.SiO2 Alite C3S
i. Tricalcium silicate(C3S)
Generates heat more rapidly
Hydrates more rapidly
Possesses less resistance to chemical attack
Develops early strength
ii. Dicalcium silicate(C2S)
Imparts ultimate strength to the cement
Offers more resistance to chemical attack
Hardens more slowly
Hydrates slowly
iii. Tricalcium aluminate (C3A)
Weak against sulphate attack
Reacts fastly, generating a large amount of heat
Does not contribute to develop strength
Causes initial setting of cement
iv. Tetra calcium aluminium ferrite (C4AF)
Poor cementing value
Reacts slowly, generating small amount of heat
Comparatively inactive
HYDRATION OF CEMENT
The chemical reaction between cement and water is known as hydration of cement. The
reaction takes place between the active components of cement (C4AF, C3A, C3S and C2S) and
water. The factors responsible for the physical properties of concrete are the extent of hydration
of cement and the resultant microstructure of the hydrated cement. When the cement comes in
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contact with water, the hydration products start depositing on the outer periphery of the nucleus
of hydrated cement. This reaction proceeds slowly for 2-5 hours and is called induction or
dormant period. As the hydration proceeds, the deposit of hydration products on the original
cement grain makes the diffusion of water to unhydrated nucleus more and more difficult,
consequently reducing the rate of hydration with time. At any stage of hydration, the cement
paste consists of gel (a fine-grained product of hydration having
large surface area collectively), the unreacted cement, calcium hydroxide, water and some
minor compounds. The crystals of the various resulting compounds gradually fill the space
originally occupied by water, resulting in the stiffening of the mass and subsequent development
of the strength.
RATE OF HYDRATION
The reaction of compound C3A with water is very fast and is responsible for flash setting of
cement (stiffening without strength development) and thus it will prevent the hydration of C3S
and C2S. However, calcium sulphate (CaSO4) present in the clinker dissolves immediately in
water and forms insoluble calcium sulphoaluminate. It deposits on the surface of C3A forming
a colloidal membrane and consequently retards the hydration of C3A. The amount of CaSO4 is
adjusted to leave a little excess of C3A to hydrate directly. This membrane in the process breaks
because of the pressure of the compounds formed during hydration and then again C3A becomes
active in the reaction.
The hardening of C3S can be said to be catalyzed by C3A and C3S becomes solely responsible
for gain of strength up to 28 days by growth and interlocking of C-S-H gel. The increase in
strength at later age is due to hydration of C2S.
The following physical properties should be checked before selecting a Portland cement for the
cement through 90 micron sieve or by surface area of cement in square centimeters per
should not be more than 10 percent. In terms of specific surface should not be less than
2250cm2/gm.
b) Setting time: A period of 30 minutes as minimum setting time for initial setting and a
provided the tests are conducted as per the procedure prescribed by IS 269-1967.
c) Soundness: Once the concrete has hardened it is necessary to ensure that no volumetric
changes take place. The cement is said to be unsound, if it exhibits volumetric instability
after hardening.
d) Crushing strength: For this mortar cubes are made with standard sand and tested in
compression testing machine as per the specification of IS code. The minimum strength
a) Fineness test: It is conducted by sieve analysis 100gms of cement is taken and sieved
through IS sieve No.9 for fifteen minutes. Residue on the sieve is weighed. This should
b) Setting time: Initial setting time and final setting are the two important physical
properties of cement. Initial setting time is the time taken by the cement from adding of
the water to starting of losing its plasticity. Vicat apparatus is used for finding the setting
times. Vicat apparatus consists of a movable rod to which any one of the three needles
mould is associated with this apparatus which is in the form of split cylinder.
Vicat apparatus
Before finding initial and final setting time it is necessary to determine water to be added to get
standard consistency. For this 300gms of cement is mixed with about 30% and cement paste
prepared is filled in the mould which rests on non-porous plate. The plunger is attached to the
movable rod of Vicat apparatus and gently lowered to touch the paste in the mould. Then the
plunger is allowed to move freely. If the penetration is 5mm to 7mm from the bottom of the
mould then cement is having standard consistency. If not, experiment is repeated with different
proportion of water fill water required for standard consistency is found. Then the tests for initial
standard consistency and vicat mould is completely filled and top surface is leveled. 1 mm
square needle is fixed to the rod and gently placed over the paste. Then it is freely allowed to
penetrate. In the beginning the needle penetrates the paste completely. As time lapses the paste
start losing its plasticity and offers resistance to penetration. When needle can penetrate up to 5
to 7mm above bottom of the paste experiment is stopped and time elapsed between the addition
Final setting time: The square needle is replaced with annular collar. Experiment is continued
by allowing this needle to freely move after gently touching the surface of the paste. Time
elapsed between the addition of water and the mark of needle but not of annular ring is found on
False set: No heat is evolved in a false set and the concrete can be re-mixed without adding
water. It occurs due to the conversion of un-hydrous/semi-hydrous gypsum to hydrous gypsum
(CaSO4.2H2O).
Flash Set: is due to absence of Gypsum. Specifically used for under water repair.
c) Soundness test: This test is conducted to find free lime in cement, which is not desirable.
Le Chatelier apparatus shown below is used for conducting this test. It consists of a split
brass mould of diameter 30mm and height 30mm. On either side of the split, there are
two indicators, with pointed ends. The ends of indicators are 165mm from the centre of
the mould.
Properly oiled Le Chatelier mould is placed on a glass plate and is filled completely with a
cement paste having 0.78 times the water required consistency. It is then covered with another
glass plate and a small weight is placed over it. Then the whole assembly is kept under water for
between the indicators. Then place the mould again in the water and heat the assembly such that
water reaches the boiling point in 30 minutes. Boil the water for one hour. The mould is removed
from water and allowed to cool. The distance between the two pointers is measured. The
difference between the two readings indicates the expansion of the cement due to the presence of
d) Crushing Strength Test For this 200gm of cement is mixed with 600gm of standard
cube mould of 70.6mm size (Area 5000mm2) kept on a steel plate and prodded with 25mm
standard steel rod 20 times within 8 seconds. Then the mould is placed on a standard vibrating
table that vibrates at a speed of 12000 + 400 vibration per minute. A hopper is secured at the top
and the remaining mortar is filled. The mould is vibrated for two minutes and hopper removed.
The top is finished with a knife or with a trowel and leveled. After 24 + 1 hour mould is removed
After specified period cubes are tested in compression testing machine, keeping the specimen on
its level edges. Average of three cubes is reported as crushing strength. The compressive strength
at the end of 3 days should not be less than 11.5 N/mm2 and that at the end of 7 days not less
MANUFACTURE OF CEMENT
i) Dry process
In this process lime stone and clay are ground separately to fine powders and are then mixed
together in the desired proportions. Water is then added to it so as to get a thick paste of which
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cakes are then made, dried and burnt in kilns. To the clinker obtained is added three to four
percent of gypsum and ground to very fine powder. This powder is cement ready for use.
This process is slow and costly. Also is difficult to have the correct proportion of constituents
and to do so is cumbersome operation. The quality of cement is not as good as that of the one
manufactured by the wet process. This method has, therefore, become obsolete and the wet
i) Collection of raw materials: Calcareous materials such as lime stone, marl, chalk etc
are quarried by blasting. Argillaceous materials such as clay, slate etc. are transported
desirable proportions are fed into ball mills. A little water too is added to it. Ball mill
is a rotating steel cylinder in which there are hardened steel balls. When the mill
rotates, the steel bails pulverize the raw material which forms into a solution with
water. The mixture is known as slurry. This slurry is then passed into storage tanks
known as silos where their proportioning is finally adjusted to ensure the correct
chemical composition. Corrected slurry is then fed into the rotary kiln for burning.
iii) Burning. Corrected slurry is fed at the higher end of the inclined rotary kiln whereas
from the lower end of the kiln flame is produced by injecting pulverized coal with a
blast of air. Rotary kiln is a steel tube lined with fire bricks. It is 90 to 120 metres
long and from 25 to 3.5 meters in diameter. The kiln is mounted on rollers at a
―nodules‖. The nodules gradually roll down passing through zones of rising
temperatures until they reach burning zone where they are finally burnt at 1500 to
16500C. At these temperatures ―nodules‖ change to clinkers. Clinkers are air cooled
iv) Grinding. Grinding of the clinker is done in large tube mills which are kept cool by
spraying water on them from outside. While grinding the clinker three to four percent
gypsum (calcium sulphate) is added so as to control the setting time of cement. Finely
STORAGE OF CEMENT
Portland cement is a finely ground material. It, therefore, readily absorbs moisture even from the
atmosphere. It is therefore essential to protect it from dampness during storage. Lack of proper
care may cause setting of cement or reduction in its strength due to partial setting. Following
i) Walls, roof and floor of the building in which cement is to be stored should be
ii) In case the cement store is newly constructed then its interior should have been
iii) Doors and windows should be properly fitted and should be kept shut.
iv) Except in case of dry concrete floor the cement bags should be stacked on wooden
planks.
v) The bags should be stacked away from walls. A space of 25cm all around should be
vii) Bags should be piled in header stretcher fashion and not more than 15 bags high
viii) While removing cement from store do not take out bags from one tier only. Step back
ix) Each incoming consignment should be stacked separately and a placard bearing date
of arrival of the consignment should be pinned to it. This would help in using cement
position for a long time while other consignments of cement come in and go out.
x) For temporary storage of cement at site of work, bags should not be stacked on the
ground. Minimum number of bags needed should be piled upon raised dry platform
USES OF CEMENT
Cement is used widely for the construction of various structures. Some of them are listed below:-
ii) Cement mortar is used for masonry work, plastering and pointing.
iii) Cement concrete is used for the construction of various structures like buildings,
iv) Cement is used to manufacture lamp posts, telephone posts, railway sleepers, piles
etc.
v) For manufacturing cement pipes, garden seats, dust bins, flower pots etc. cement is
commonly used.
vi) It is useful for the construction of roads, footpaths, courts for various sports etc
In addition to ordinary Portland cement there are many varieties of cement. Important varieties
The OPC- 53 is produced using a highly specialized process that allows optimum distribution of
each particle, thereby allowing superior crystalline structure and balanced composition. The
result is better strength and durability. OPC - 43 grade cement is produced by inter grinding of
clinker and gypsum, to an optimum fineness to ensure both strength & durability of concrete at
all ages, which it suitable for all construction works.
The cost of producing OPC is very low and available at the best quality because of the readily
available raw material in the area where it is produced. Being low cost cement it is widely used
in the production of concrete, which is the most popular material used for construction of roads,
houses, buildings, dams etc. Ordinary Portland cement is also used for mortars and in making
grouts.
ii) White cement. The cement when made free from colouring oxides of iron,
manganese and chromium results into white cement is used for the floor finishes,
plastering, omamental works etc. In swimming pools white cement is used to replace
iii) Coloured cement: The cement of desired colours are produced by intimately mixing
pigments with ordinary cement. The chromium oxide gives green colour. Cobalt
produce blue colour. Iron oxide with different proportion produce brown, red or
yellow colour. Addition of manganese dioxide gives black or brown coloured cement.
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These cements are used for giving finishing touches to floors, walls, window sills,
roofs etc. These cements are used for making terrazzo flooring, face plaster of walls
iv) Quick setting cement: Quick setting cement is produced by reducing the percentage
of gypsum and adding a small amount of aluminium sulphate during the manufacture
of cement. Finer grinding also adds to quick setting property. This cement starts
setting within 5 minutes after adding water and becomes hard mass within 30
v) Rapid hardening cement: This cement can be produced by increasing lime content
and burning at high temperature while manufacturing cement. Grinding to very fine is
also necessary. Though the initial and final setting time of this cement is the same as
that of Portland cement, it gains strength in early days. This property helps in earlier
removal of form works and speed in construction activity. It is suitable for repair of
roads and bridges and when load is applied in a short period of time.
vi) Low heat cement: In mass concrete works like construction of dams, heat produced
due to hydration of cement will not get dispersal easily. This may give rise to cracks.
Hence in such constructions it is preferable to use low heat cement. This cement
contains low percentage (5%) of tricalcium aluminate (C3A) and higher percentage
(46%) of dicalcium silicate (C2S). It is most suitable for large mass concrete works
vii) Pozzolana Cement: Pozzolana is a volcanic power found in italy. It can be processed
from shales and certain types of clay also. In this cement pozzolana material is 10 to
30 percent. It can resist action of sulphate. It releases less heat during setting. It
strength is low. It is used for mass concrete works. It is also used in sewage line
works.
viii) Expanding cement: This cement expands as it sets. This property is achieved by
adding expanding medium like sulpho aluminate and stabilizing agent to ordinary
bauxite. It is more resistant to sulphate and acid attack. It develops almost full
strength within 24 hours of adding water. It is used for under water works. It has low
heat evolution and is used in the places of mass concrete such as dams and in places
of high temperature.
x) Blast furnace cement: In the manufacture of pig iron, slag comes out as a waste
cement is produced. The properties of this cement are more or less same as ordinary
cement, but it is cheap, since it utilize waste product. This cement is durable but it
gains the strength slowly and hence needs longer period of curing.
xi) Acid Resistant Cement: This cement is produced by adding acid resistant aggregate
such as quartz, quartzite, sodium silicate or soluble glass. This cement has good
chemical factories.
C3A below five percent in ordinary cement this cement is produced. It is used in the
xiii) Fly Ash Blended Cement: Fly ash is byproduct in thermal stations. The particles of
fly ash are very minute and they fly in the air, creating air pollution problems.
Thermal power stations have to spend lot of money to arrest fly ash and dispose
safety. It is found that one of the best ways to dispose fly ash is to mix it with cement
in controlled condition and derive some of the beneficiary effects on cement. Now a
days cement factories produce the fly ash in their own thermal stations or borrow it
from other thermal stations and further process it to make it suitable to blend with
Fly ash blended cements have superior quality of resistance to weathering action. The ultimate
strength gained is the same as that with ordinary Portland cement. However strength gained in
5.2 LIME
Lime is a very important building and construction material, which has been in use since ancient
time for plastering, mortar and concrete works. Lime is still today as important building material
PROPERTIES OF LIME
Following are properties of lime, which makes it a very important engineering material:
(vi) Its shrinkage is comparatively low and hence masonry in lime mortar is more durable
USES OF LIME
(xii) When used in combination with cement, its properties are modified and a lot of
Lime does not occur in nature in a free state. It is obtained from substances having a lot of
calcareous content in it e.g. limestone, chalk. All these substances have calcium carbonate
(CaCO3) as the chief constituent. When heated, carbon dioxide and moisture are driven out
(i) Calcination. This is a process of heating the lime stone to redness in the presence of air
During calcination, carbon dioxide is driven off and calcium oxide is left as the final product,
which is lime.
(ii) Quicklime. Lime obtained from the calcination of pure limestone is known as quick lime.
This has a high affinity to water/moisture. It is essentially calcium oxide but sometimes small
(iii) Setting of lime. When lime is converted in to paste form and then exposed to the
(iv) Slaking/ slacking. Quick lime has a high affinity for moisture. Adding of water in
(v) Slaked lime. Water required for slaking lime is about 32% of the weight of quicklime.
lime, water required in the slaking is taken 2-3 times the volume of the quicklime.
Hydrated lime is then obtained in form of dry powder, which is sold in packed bags.
Slaked lime should be used fresh because it has the tendency to absorb carbonic acid
When slaked lime is converted into carbonate of lime, it becomes spoiled because it loses its
setting property and hence slaked lime should not be kept in a damp place.
CLASSIFICATION OF LIME
Composition of various limestone differs considerably and there are numbers of different kinds
of limes each having characteristic properties which influence the purposes for which they are
used.
iv) Magnesian
This lime contains less than 5% of impurities such as silica or alumina (in form of clay). In the
analysis, the specimen is shown consisting almost entirely of calcium oxide (about 93%). It
slakes rapidly, evolves much heat, and expands to 2-3 times its original bulk during slaking. It
has a high degree of plasticity (hence the name fat), is slow setting and very slow in hardening.
This stiffening can only occur when the lime is in contact with air.
Pure lime is white in colour, is used extensively for plastering, not so suitable for mortar because
This consists of more than 5% of the impurities of silica, alumina and iron oxide. It is therefore
less pure than fat lime. It contains about 82% of CaO. Characteristics are similar to those of fat
lime by on account of its impurities, it slakes less rapidly (resulting in a diminution of heat and
volume). Its iron content is responsible for its grey colour. Like fat lime, it sets and hardens
This class of lime is capable of setting and hardening when not in contact with air and even
submerged in water, hence the name hydraulic. Limestone from which hydraulic lime are
prepared contain varying properties of silica, and alumina in the form of clay and iron oxide. It
contains about 67% of CaO. The clay and iron oxide play an important part in the setting and
When the limestone is burnt, CO2 dioxide driven off and calcium oxide formed, it has a strong
affinity for clay, and combines with it to form silica and aluminates of lime.
If water is added to this burnt product after it has been finally ground, the mass begins to set an
harden as the water combines with the various products. This action is not dependent on the
presence of CO2 and therefore will continue even when air is not present. The setting and
hardening are similar to Portland cement. These hydraulic lime are subdivided into 4 types.
a) Feebly hydraulic lime: This contains less than 15% of silica and alumina. The rate of
mortar.
b) Moderately hydraulic lime: Alumina and silica content is about 15-25%. Slaking is
slow and expansion is small. It makes excellent mortar, is stronger than feebly hydraulic
c) Eminently or very hydraulic: This type contains 25-30% of the important constituents
is silica and alumina. Chemical composition is very similar to that of Portland cement
and screened before use to eliminate coarse un slaked particles. It closely resembles Portland
The rocks from which such limes are produced are known as magnesium limestone or dolomitic
they contain up to 45% magnesium carbonate. When calcinations takes place, the finished
Magnesium oxide has similar characteristics to calcium oxide although it slakes much more
quick. When more than 5% of magnesium oxide is present; the finished product is classified as
magnesium lime.
MANUFACTURE OF LIME
Following three distinct operations are involved in the manufacture process of lime:
The lime stones of required quality are collected at site of work. For fat lime, the percentage of
impurities in lime stones should not exceed 5 per cent. It is desirable to use comparatively pure
The calcination or burning of lime stones to bright red heat is the next important operation. The
fuel required for calcination of lime stones may consist of charcoal, coal, firewood or coal ashes.
The initial firing is achieved with the help of few chips of dry wood or cow-dung cakes. As in
case of bricks, the burning of lime stones can be achieved either in clamps or kilns. The clamps
The kilns are permanent structures and they may be of intermittent type or continuous type.
The burning of lime stones is thus carried out in one of the following:
(i) Clamps
Mortars may be defined as mixtures of sand, and binders such as lime or cement and water. The
mortar can also be defined as the bedding materials used for bricks, blocks and masonry in cases
The prime function of mortars is to take up tolerance between building units such as bricks,
blocks and stones. Before properties and uses of the different types of mortar are explained, let
us look closely the fine aggregate known as sand. Sand is used as an inert material in mortars and
concretes.
It is a form of silica (SiO2), which may be siliceous, argillaceous according to composition. Sand
particles consist of small grains of silica. It is mostly obtained from pits, shores, river beds and
sea beds. Sand is formed by the disintegration of rocks by weathering. Sand may be classified in
Pit sand is obtained by forming pits in to the soil and the sand excavated out. It is sharp, angular,
porous and free from harmful salts. Clay and impurities should be washed and screened.
coarse. There are chances of fine sand having silt and should therefore be washed out before use
Sea sand- This consists of fine rounded grains of brown colour and is collected from the sea
beach. Usually contain salt which attracts moisture from the atmosphere and causes
disintegration of work in which it is used. It can be used locally after it has been thoroughly
Stone dust- This is obtained during the crushing of stone to obtained coarse aggregates. This
size of stone dust is the size of sand. Stone dust from good quality stone is an excellent fine
aggregate. Using stone dust of the same stone, a mortar matching the colour of stone masonry
Sand may be divided in to three categories; fine sand, coarse sand and gravely sand. Fine sand is
used mostly for plaster work, coarse sand for masonry work and gravely sand for concrete work.
Bulking of sand
Bulking of sand means the increase in its volume. Fine aggregates or sand increases in volume
when it possesses some moisture. Bulking is due to formation of a thin film of water around the
fine aggregate or sand particles. Thickness of water around the fine aggregate goes on increasing
with moisture and consequently increase in volume continues. However, after a certain
percentage water, volume of sand starts decreasing with increasing amount of water and at a
(iv) Clay and soil are considered harmful ingredients; their amount should not exceed 4% in this
case of natural sand and ground gravel. In sand or grit obtained from stone (i.e. stone dust) their
(v) It should not be too fine. It should be coarse and clean and free from all sorts of deleterious
materials.
(vi) It should be well graded so that minimum voids are left in it. This amount will require a less
(i) Bulk-It increases the volume of the mortar and consequently makes mortar more
economical.
(ii) Sand prevents excessive shrinkage of the mortar. This aspect avoids cracking of the
(iii) It helps in the setting action of fat lime mortars. Atmospheric air containing carbon
dioxide can reach lime through voids of sand and cause its setting.
(iv) Strength of the mortar or concrete can be adjusted by addition of larger or smaller
amounts sand.
(v) Since sand is an inert material, it renders the structure more resistant against
atmosphere agencies.
Properties of mortar
(i) Good workability in the plastic state but with sufficient early stiffening to prevent
joint squeezing.
(ii) Good water retentivity (the mixing water should not bleed out)
(iii) Adequate cohesion in the plastic state to ease handling and reduce droppings.
(iv) Adequate adhesion to the bedded units both in the plastic and hardened state. the term
(vi) Durability should be sufficient with regard to the degree of exposure likely and any
(vii) Tolerable drying shrinkage and moisture movement where this relevant to the of
proposed work.
(viii) They should permit movement (unless this is negligible or movement joints are
take the form of micro crack within the mortar rather than cracking in the bricks or
blocks
In practice, any improvement in any one of these properties can readily be achieved by varying
the mix proportions or constituents but usually to the detriment of one or more of the other
(a) An increase in cement content results in a stronger mortar but drying shrinkage is
increased.
(b) The use of finer sand in a mix improves its cohesion, water retentivity and workability
(c) The cost of material is an important factor and there is usually the need to limit the
cement content (because it is the most expensive material) thus limiting the strength
Cement mortars
Cement mortars consists of a mixtures of cement, sand and water in suitable proportions. The
proportion of cement to sand by volume varies from 1:2 to 1:6 or even more. Cement mortar is
the strongest of all the mortars and is commonly used in work which is below the ground level
dpc, to very exposed work such us free standing walls and parapets to engineering constructions
with bricks of high strength (i.e. in load bearing wall, pillar columns etc.). All these are cases
Cement is measured in bags one cement bag is 50kg in weight and 351itres in volume (sand is
used in volume but allowance needs to be made for bulking). Cement and sand are mixed in
required proportions in dry states on an impervious platform. The contents are mixed two to
Dry mix can be taken in pans to the place of work and water added by the mason himself when
he intends to use it or water can be added at the mix place to achieve the required workability.
On big sites where water mortar supply is continuously required. Mixer machines may be used.
Any mixture containing cement should be used up within 2 hours of mixing. The addition of
further water after first mixing known as re-tempering should not be permitted. However,
mortar within permissible working period without detriment to the final strength of the mortar.
Mortar mixes are classified in BS 5628 part three cement sand mortars for masonry work varies
from1:2 to 1:8.
Lime mortars
In this type of mortars, lime (fat lime or hydraulic lime) is used as a binding material.
One of its characteristics is the continued strength development over long periods.
Slaked fat lime is used to prepare mortar to be used for plastering and hydraulic lime is used in
During setting, lime shrinks considerably and hence 2 to 3 times its volume of sand is added to
If fat lime is used in the mortar, it should be slaked before use. Fat lime mortar is unsuitable for
water logged and damp conditions. If hydraulic lime is used, proportion of lime to sand by
volume is above 1-2; this mortar should be used within one hour of fixing. This mortar can
withstand damp condition and is stronger than fat lime mortar. 1:2 or 1:3 lime sand mortar is
Lime mortar was once the principal material used for bedding and joining bricks, stones etc. it is
used less frequently now because it develops strength very slowly. If mixed by hand, the lime is
placed in heap, sprinkled with water and completely covered with the measured proportion of
sand. The lime expands and breaks in to small particles owing to the heat generated, this is
thorough disintegration of the lime. Unslaked lime particles of the lime in mortar may cause
damage to walling. It is necessary to pass it through a screen to eliminate unslaked lime particles.
After slaking, the material is turned over with a shovel or a boarded platform. More water is
added and the mixing continued until the mortar is of the right consistency, neither too stiff not
too plastic.
If mixed in a pug mill, the lime and sand are thoroughly ground and mixed after about 20
The mortar should be used fresh and just sufficient amount should be mixed for each day‘s use.
For other types of work, a strong mortar is both unnecessary and undesirable. Unfortunately, the
use much weaker cement mortars (i.e. low cement content) is not practicable because it results in
These deficiencies can be reduced by the inclusion of lime in the mortar thus explaining the
The lime increases the water retentively of the mortar, prevents excessive withdrawal of water
necessary for laying the units and for the hydration of the cement by units of high suction.
including lime, the ratio of sand to cement can be doubled i.e. twice that of a cement mortar.
Lime mortar is mixed as above and then gauge (add) to this mixture the necessary proportion of
Portland cement immediately before the mortar is required for use. Compo mortar is more open-
moderate or low strength. The proportions vary from 1 part cement to 2-3 parts to 6-9 parts sand.
MORTAR PLASTICISERS
Mortar plasticizers are liquids when added to water effervesce i.e. mixture becomes bubbly like
so water.
When used in small quantities, millions of minute bubbles form around the sand particles and so
Plasticity is increased so that there is no need to use lime. Plasterers do not adversely affect the
The application of interior and external finish to structure is usually the final phase in the
construction of buildings.
Functions of plaster
1) Strength. The strength of plaster should be less than that of background so as to allow
bonding.
2) Porosity. Both affect the adhesion of the plaster system to the background and there for
it‘s ultimate strength.
3) Bond. The plaster must be able to key to the plaster. The key may be provided artificially
by raking out the mortar joints on brickwork or naturally by the background material
itself as in the case of more fine concrete.
4) Trueness of construction. Since plaster is to provide a smooth surface excessive filling
of surface undulation may require a number of coats or very thick layers of plaster which
will affect its adhesion characteristics of the wall and the condition the wall shall be
subjected to control moisture movement.
PLASTERING PROCESS
A maximum of 3 coats are used for plastering and each having its own function.
Applying mortar coats on the surfaces of walls, columns, ceiling etc. to get smooth finish is
termed as plastering. Mortar used for plastering may be lime mortar, cement mortar and
lime cement mortar. Lime mortar used shall have fat lime to sand ratio of 1: 3 or 1: 4. If
hydraulic lime is used mix proportion (lime: sand) is 1:2. Cement mortar of 1: 4 or 1: 6 mix
is very commonly used for plastering, richer mix being used for outer walls. To combine the
cost effectiveness of lime mortar and good quality of cement mortar many use lime-cement
mortar of proportion (cement: lime: sand) of 1: 1: 6 or 1:1:8 or 1:2:8.
Method of Plastering:
The plastering could be done on the surfaces either in one, two and three coats. The plastering‘s
for two coats are as follows:
Defects in Plastering
The brickwork and plastering should be carried out in the best workmanship manner.
The bond of brickwork should be maintained properly.
The efflorescence is removed by rubbing brushes on damaged surfaces. A solution of one
part of HCl or H2SO4, and five parts of clean water is prepared and it is applied with the
help of brushes on affected area. The surface is washed and cleaned with water.
The bricks of superior nature should only be used for the brick work.
The water free from salts should be used for brick work and plastering work.
The surface to be plastered should be well watered so that it may not absorb water from
plaster.
The damp- proof courses should be provided at convenient places in buildings.
The overall construction should be such that the penetration of moisture is prevented.
The fresh plastered surface should be protected from surplus quantity of water such as
rain and excessive heat such as sun.
Lime mortar is usually applied in 3 coats while cement mortar is applied in two or three
coats for the stone and brick masonry. For concrete surfaces cement mortar may be applied
in two or three coats. For concrete building blocks many times only one coat of cement
mortar is applied. The first coat provides means of getting level surface. The final coat
provides smooth surface. If three coats are used second coat is known as floating coat. The
average thickness of first coat is 10 to 15 mm. Middle coat thickness is 6–8 mm. The final
coat is just 2 to 3 mm thick. If single coat is used its thickness is kept between 6 to 12 mm.
Such coats are used on concrete surfaces not exposed to rain. The mortar used for
plastering work can be classified into three categories:
1) Lime mortar: it consists of equal volume of lime and sand these two materials are
carefully ground in mortar mill. Flat lime is recommended for plastering work.
IV. Keene’s Plaster: This is the hard burnt or dead – burnt anhydrous gypsum plaster
obtained by heating gypsum to temperature of about 6000C to give relatively inert
product. An addition of 0.5 – 1.0% potash alum or potassium sulphate accelerator is
added to accelerate the rate of crystallization to produce setting when water is added. A
slow but continuous set occurs which makes it suitable for finishing only. Both classes C
and D plasters hydrate or set into the dehydrate form. Typical trade names of the class
include keene‘s cement, parian cement, superite.
However, if calcination of gypsum is carried out at a much higher temperature (e.g 1100
– 1200oC). Some decomposition into calcium oxide and sulphur trioxide occurs and solid
solution of CaO in CaSO4 if formed. This is the basis of the estrich gips, the germain
flooring, plaster which has a very slow set.
Concrete is a composite material composed mainly of water, aggregate, and cement. Often,
additives and reinforcements are included in the mixture to achieve the desired physical
properties of the finished material. When these ingredients are mixed together, they form a fluid
mass that is easily molded into shape. Over time, the cement forms a hard matrix which binds the
rest of the ingredients together into a durable stone-like material with many uses.
INGREDIENTS OF CONCRETE:
Cement: The cement powder, when mixed with water, forms a paste. This paste acts like
glue and holds or bonds the aggregates together.
Aggregates: Aggregates are of two basic types: COARSE: crushed rock, gravel or
screenings. FINE: fine and coarse sands and crusher fines.
Water: Water is mixed with the cement powder to form a paste which holds the aggregates
together like glue. Water must be clean, fresh and free from any dirt, unwanted chemicals
or rubbish that may affect concrete.
Admixtures: Admixtures are mixed into the concrete to change or alter its properties, ie
the time concrete takes to set and harden, or its workability.
i. Strength. Concrete should be able to withstand the stresses that it is subjected to. It
is quite strong in compression but weak in tension.
ii. Durability. It should be able to withstand the weathering action such as of wind,
rain, frost and variations of temperature.
iii. Density. The concrete should be well compacted so that there are no voids or
hollows left.
Advantages of Concrete
i. Ingredients of concrete are easily available in most of the places.
ii. Unlike natural stones, concrete is free from defects and flaws.
iii. Concrete can be manufactured to the desired strength with an economy.
iv. The durability of concrete is very high.
v. It can be cast to any desired shape.
vi. The casting of concrete can be done in the working site which makes it economical.
vii. The maintenance cost of concrete is almost negligible.
viii. The deterioration of concrete is not appreciable with age.
ix. Concrete makes a building fire-safe due to its noncombustible nature.
x. Concrete can withstand high temperatures.
xi. Concrete is resistant to wind and water. Therefore, it is very useful in storm shelters.
Disadvantages of Concrete
i. Compared to other binding materials, the tensile strength of concrete is relatively low.
ii. Concrete is less ductile.
iii. The weight of concrete is high compared to its strength.
iv. Concrete may contain soluble salts. Soluble salts cause efflorescence.
In order to obtain good workable concrete the properties used are classified into two states
which include;
The following are the properties of concrete when it is in its plastic or wet state;
Workability:
It is defined as the ease with which concrete can be mixed, transported, placed and
compacted fully without any segregation and bleeding. It depends on the quality of water
grading of aggregates and the percentage of fine materials in the mix.
Segregation:
Segregation can be defined as the separation of the constituent materials of concrete. A good
concrete is one in which all the ingredients are properly distributed to make a homogeneous
mixture. If a sample of concrete exhibits a tendency for separation of say, coarse aggregate from
the rest of the ingredients, then, that sample is said to be showing the tendency for segregation.
Such concrete is not only going to be weak; lack of homogeneity is also going to induce all
undesirable properties in the hardened concrete. There are considerable differences in the sizes
and specific gravities of the constituent ingredients of concrete. Therefore, it is natural that the
materials show a tendency to fall apart.
Segregation may be of three forms;
i. Firstly, the coarse aggregate separating out or settling down from the rest of the matrix,
ii. Secondly, the paste or matrix separating away from coarse aggregate.
iii. Thirdly, water separating out from the rest of the material being a material of lowest
specific gravity.
Segregation results in honey combing, decrease in density and ultimately loss of strength of
hardened concrete.
Fully cured, hardened concrete must be strong enough to withstand the structural and
service loads which will be applied to it and must be durable enough to withstand the
environmental exposure for which it is designed. If concrete is made with high-quality
materials and is properly proportioned, mixed, handled, placed and finished, it will be the
strongest and durable building material.
Strength: When we refer to concrete strength, we generally talk about the compressive
strength of concrete. Because concrete is strong in compression but relatively weak
in tension and bending. It mostly depends upon amount and type of cement used in concrete mix.
It is also affected by the water-cement ratio, mixing method, placing and curing.
Concrete tensile strength ranges from 7% to 12% of compressive strength. Both tensile strength
and bending strength can be increased by adding reinforcement.
Durability: Durability might be defined as the ability to maintain satisfactory performance over
extended service life. Different concretes require different degrees of durability depending on the
exposure environment and properties desired. Appropriate concrete ingredients, mix proportions,
finishes and curing practices can be adjusted on the basis of the required durability of concrete.
Shrinkage: Shrinkage is the volume decrease of concrete caused by drying and chemical
changes. In other words, the reduction of volume for the setting and hardening of concrete is
defined as shrinkage.
Water Tightness: Another property of concrete is water tightness. Sometimes, it‘s called
impermeability of concrete. Water tightness of concrete is directly related to the durability of
concrete. The lesser the permeability, the more the durability of concrete.
TYPES OF CONCRETE
1) Plain concrete
The plain concrete will have no reinforcement in it. The main constituents are the cement,
aggregates, and water. Most commonly used mix design is 1:2:4 which is the normal mix design.
The density of the plain concrete will vary between 2200 and 2500 Kg/meter cube. The
compressive strength is 200 to 500 kg/cm2. These types of concrete are mainly used in the
construction of the pavements and the buildings, especially in areas where there is less demand
of high tensile strength. The durability given by this type of concrete is satisfactory to high
extent.
2) Reinforced cement concrete (R.C.C)
This concrete wherein steel bars have been embedded to enable it take up tension/shear
stresses safely is known as reinforced cement concrete. It is used in the construction of all
sorts of buildings, bridges, arches, tanks and massive dams etc.
The reinforcement material for concrete should possess the following characteristics.
1. The coefficient of linear expansion of concrete and steel are almost the same. Therefore
no internal stresses are set up within reinforced concrete due to change in temperature.
2. The coating of cement on the surface of steel bars protects them from corrosion and
doesn‘t produce an adverse chemical effect.
3. The concrete while setting grips very first to the surface of steel bars. So the concrete is
able to transmit to the steel bars those stresses which cannot resist itself.
BAR NOTATIONS
Is fire resistant.
It doesn‘t rot or decay.
It is impermeable.
Does not develop cracks easily.
It is durable.
It is manufactured with high grade controlled concrete having three to four times the
strength of concrete normally used in R.C.C. High tensile steel with breaking strength
nearly four times the strength of the normal mild steel used in R.C.C. is used in case of
prestressed cement concrete.
Prestressed concrete is produced in factory. This is concrete in which high tensile wires are
pulled between two anchors. The concrete is cast to the required shape around this wire. The
wires are released from the anchors after the concrete has gained its strength and this is called
PRE-TENSIONING. In other cases the concrete is cast in wires before stressing them but the
wives are stressed before the real setting of concrete after the concrete has gained strength the
anchors are pulled and this is called POST-TENSIONING. In either case the tendency of the
Prestressed beams, girders, flooring, roofing, bridge girders, railway sleepers, fencing posts
and number of other components are extensively used.
Advantages
USES
Harsh mix. Have bigger or more coarse aggregates in the mix. Not easily workable.
Poor mix. Has poor proportions of ingredients sometimes used for binding
4) Aerated concrete
It is manufactured from calcareous and siliceous materials like cement, lime, pulverized
sand, fly-ash etc. Air cells are entrapped in it. Presence of air cells makes the material light,
impervious to water and a nice insulator. It can be produced in varying densities depending
upon the use to which it has to be put. It can be used from mere lining materials for cold
storages (because of its insulation properties) to load bearing slabs for roofs and floors. If
needed it could be reinforced like ordinary concrete.
5) Pre-packed concrete
6) Foam concrete
This light weight concrete is being produced in various varieties, having different
properties each suited for a specific purpose and possesses excellent heat insulation
properties, especially in lighter forms. It is used for heat insulation over roofs etc; light
weight partition walls, light weight roofs for factories and for light weight false ceiling.
7) Precast Concrete
Various structural elements can be made and cast in the factory as per the specifications and
brought to the site at the time of assembly. Such concrete units are called as the precast concrete.
The examples of precast concrete units are concrete blocks, the staircase units, precast walls and
poles, concrete lintels and many other elements. These units have the advantage of acquiring
speedy construction as only assemblage is necessary. As the manufacturing is done at site,
quality is assured. The only precaution taken is for their transportation.
9) Shotcrete Concrete
Here the concrete type differs in the way it is applied on the area to be cast. The concrete is shot
into the frame or the prepared structural formwork with the help of a nozzle. As the shooting is
carried out in a higher air pressure, the placing and the compaction process will be occurring at
the same time.
PRODUCTION OF CONCRETE
A good quality concrete is essentially a homogeneous mixture of cement, coarse and fine
aggregates and water which consolidates into a hard mass due to chemical action between
the cement and water. The stages of concrete production are: Batching or measurement of
materials, Mixing, Transporting, Placing, Compacting, Curing and Finishing.
1. Batching of materials
It is the process of measuring concrete mix ingredients either by volume or by weight and
introducing them into the mixture. Batching can be done in two ways.
a) Volume batching
i. Batching of cement: It is always measured by weight mostly used in terms of bags each
weighing 50 kg and volume of 35 litres (0.035m3). Cement should be batched by volume
because its weight per volume varies.
ii. Batching of aggregates: A gauge box is used for batching fine and coarse aggregates by
volume. The box shouldn‘t be too shallow and should be completely filled and the top be
struck off.
When batching by volume is used, possible sources of error could lead to variation in the amount
of aggregate in a specific volume and errors in measured volume. These errors often lead to
variations in the fresh and hardened properties of concrete as against specified characteristics
properties.
NB. The moisture present in aggregates and the bulking of sand must be accounted for while
using volume batching
Example
A concrete mix is specified to be 1:2:4 by volume with water content ratio of 0.6 also if the
moisture cement in fine aggregates is 6% with 20% bulking and water in the coarse aggregates is
1.5% by volume. Fine the quantities of different materials required for one bag of cement.
Solution
Ratio = 1:2:4
1 – Cement
2 – Sand
4 – Coarse aggregates
Water
1.5% =
= 22.86 litres.
b) Weight batching
In weight batching the ingredients of concrete are measured by weight generally is used in
construction where quality of concrete is required. Weight batching is more accurate than
volume batching. Large weight batching plants have automatic weighing equipment‘s and this
are supervised by experienced engineers, batching of concrete is based on bag of cement or its
multiplies unless bulking cement is used and weighed separately.
Nominal mix is batched by weight using regularly maintained and well-calibrated equipment,
therefore high degree of uniformity in proportion of the fresh and hardened state concrete can be
achieved.
Water for mixing is weighed out precisely as a function of the weight of cement used for each
mix proportion. Hence uniform water-cement ratio can be maintained, which plays an important
role in achieving strength of concrete.
The mixing operation consists of rotation or stirring, the objective being to coat the surface
of all aggregate particles with cement paste, and to blind all the ingredients of the concrete
into a uniform mass; this uniformity must not be disturbed by the process of discharging
from the mixer. The mixing may done by hand mixing and by mechanical means like,
Batch mixer, Tilting drum mixer, Non tilting drum mixer, Pan type mixer, Dual drum
mixer or Continuous mixers.
There are no general rules on the order of feeding the ingredients into the mixer as this
depend on the properties of the mixer and mix. Usually a small quantity of water is fed
first, followed by all the solids materials. If possible greater part of the water should also be
fed during the same time, the remainder being added after the solids. However, when using
very dry mixes in drum mixers it is necessary to feed the coarse aggregate just after the
small initial water feed in order to ensure that the aggregate surface is sufficiently wetted.
Methods of mixing
1. Hand mixing. It is used for small works and where machine (mixer) is not available.
Procedure.
For quality works mixing is carried out by mixer. Mixers can be broadly classified as batch
mixers and continuous mixers. The batch mixers produce concrete batch by batch with time
interval, whereas continuous mixers produce concrete continuously till plant is working.
Continuous mixers are used for large size works, e.g., dams.
a). Batch mixers are used for small and medium size works. Batch mixer may be of pan type or
drum type. The drum type may be further classified as tilting (T), non-tilting (NT), or reversing
(R) type, based on the technique of discharging the mixed concrete.
i) The tilting mixers may be hand fed or loader (skip) fed. The mixer is generally bowl shaped
or doubles conical frustum type. It can be tilted into different positions for charging, mixing and
discharging concrete. Blades are fixed inside the drum. The revolving drum with the mixing
blades gives lifting and free fall to the mix, combes and agitates it. The mixed concrete is
discharged from the open top of the drum by tilting it downwards. The concrete tips out rapidly
under gravity in an unsegregated mass as soon as the drum is tilted. These mixers may be used to
their advantage for mixes of low workability and containing large size aggregate. The
disadvantage of these mixers lies in the fact that some mortar adheres to the drum and is left out
in the drum during discharging.
ii) Non – tilting mixer. It consists of a Non-tilting cylindrical drum with blades inside and two
circular openings at the two ends. The drum rotates about a horizontal axis. The ingredients are
fed from one opening and the mix discharged from the other opening at the other end by at
inclined chute. The drawback is the segregation that occurs owing to slow rate of discharge.
iii) Reversing Drum Mixer. These are also known as forced action type mixers and are used for
3. Transportation of concrete
Concrete should be transported to the place of deposition at the earliest without the loss of
homogeneity obtained at the time of mixing. A maximum of 2 hours from the time of mixing is
permitted if trucks with agitator and 1 hour if trucks without agitators are used for transporting
concrete. Also it should be ensured that segregation does not take place during transportation and
placement. The methods adopted for transporting concrete depend upon the size and importance
of the job, the distance of the deposition place from the mixing place, and the nature of the
terrain. Some of the methods of transporting concrete are as below:
1. Irons pans used for small works and limited access however it is tedious slow and
costly.
2. Wheel barrows. Used for major quantities of works and for moderate distances.
3. Truck mixer. Used in big or large construction sites and very long distances.
4. Belt conveyors. Used for continuous vertical transportation of concrete at higher
levels it is advisable to cover it with sheets of metal to safe guard concrete from rain.
5. Chutes. Used when concrete is to be placed below the ground level chutes may be
made of corrugated iron sheets or timber.
6. Crane / Hoist. Used in tall structures to lift the concrete to the required height.
7. Pumps. Used when large quantities of concrete is to be transported locally to
congested sites concrete can be pumped to a distance of 300m horizontally or about
40 m vertically.
4. Placing of concrete.
To achieve quality concrete it should be placed with utmost care securing the homogeneity
achieved during mixing and the avoidance of segregation in transporting. Research has shown
5. Compaction of concrete.
Compaction is the process that expels entrapped air from freshly placed concrete and packs
the aggregate particles together so as to increase the density of the concrete.
A monolithic mass is created between the ends of the member, planned joints or both.
The formwork is completely filled to the intended level.
The entrapped air is expelled.
All reinforcement, tendons, ducts, anchorages and embedment‘s are completely
surrounded.
The specified finish to the formed surfaces of the member is provided.
The required properties of the concrete can be achieved.
6. Curing of Concrete
It is a process of keeping concrete wet to enable it to attain full strength. The process of keeping
concrete damp for this purpose is known as curing. The strength and hardness of concrete is due
to chemical reaction of cement and water. This reaction takes about 3 weeks, so curing should be
done for a period of 10 days – 3 weeks.
Reasons for curing concrete;
There are many methods of keeping concrete wet until, it gains its maximum strength and these
methods depend on climate conditions, the nature of the work and the cost. This methods
include.
1. Shading concrete.
2. Covering the surface with water proof paper, sand saw dust etc.
3. Sprinkling water on concrete surface.
4. Coating the concrete surface with layer of water proofing compounds.
5. Ponding
6. Hot water steam.
7. Drip irrigation.
7. Finishing of concrete
Concrete is basically used because of its high compressive strength. However, the finish of the
Ultimate product is not that pleasant. In past couple of decades efforts have been made to
develop surface finishes to give a better appearance to concrete surfaces and are as follows.
Formwork finishes: Concrete takes up the shape of the form, A variety of looks can be had to
the architects imagination. By careful preparation of formwork, proper mix design and good
workmanship smooth surfaces can be achieved. Prefabrication units can be produced to a fine
finish.
FORMWORK;
Workability of concrete is defined as the ease and homogeneity with which a freshly mixed
concrete or mortar can be mixed, placed, compacted and finished. Strictly, it is the amount
of useful internal work necessary to produce 100% compaction.
Workable concrete shows very less internal friction between particles and overcomes the
frictional resistance with just the amount of compacting efforts provided. Workability of the
concrete depends on a number of interrelating factors. Water content, aggregate properties, use
of admixtures, fineness of cement are the factors affecting workability.
1. Water content: The increase in water content increases the fluidity of the concrete thus
providing greater lubrication. This helps to increase the workability of the concrete.
Increasing the water content should be the last resort to improve the workability in the
concrete as this will seriously affect the strength of the concrete.
2. Size of aggregates: The surface area of bigger aggregates is less and hence less amount
of water is required for lubricating the surface to reduce the friction. Thus the concrete
having large sized aggregate is more workable (of course, within certain limits).
3. Mix proportions: Aggregate/ cement ratio is the measure of how lean or rich the
concrete is. If aggregate/ cement ratio is higher, the concrete becomes leaner. In lean
concrete less paste is available for the lubrication of the aggregate, while in rich concrete
with low a/c ratio, more paste is available which makes the mix more cohesive and hence
provides better workability.
4. Shape of aggregates: Rounded aggregates have considerably less surface area and less
voids in comparison to angular or flaky aggregates which provide better possibility of
overcoming the frictional resistance. Further, angular and flaky aggregates make concrete
very harsh.
5. Surface texture of aggregates: The aggregates having smooth or glossy texture have
less surface area compared to rough textured aggregates. This provides better workability
as less amount of water is required for lubricating effect. But, taking into account the
MEASUREMENTS OF WORKABILITY
a. Slump test
It is the most common method for measuring the workability of freshly mixed concrete. It can be
performed both in lab and at site. Uniformity of the concrete regarding workability and quality
A steel mould in the form of frustum of cone is used in slump test which has the top diameter of
100 mm, bottom diameter of 200 mm and the height is 300 mm. According to standard
specification, the maximum size of the aggregate in concrete that can be used to perform slump
test is restricted to 38 mm.
Apparatus
Iron pan to mix concrete, slump cone, spatula, trowels, tamping rod and graduated cylinder.
This test is generally carried out in laboratory but can be used in site also. It is particularly useful
for concrete mixes of very low workability (or very dry concrete) as they are insensitive to slump
test. This test works on the principle of determining the degree of compaction achieved by a
standard amount of work done by allowing the concrete to fall through a standard height.
Top
Topdiameter
diameter Bottom
Bottom
Top diameter
diameter
diameter Bottom
Top diameter
diameter Bottom
Top diam
diam
Container (mm)
(mm) (mm)
(mm)
(mm) Height
Height
(mm)
(mm)
(mm)(mm) Height
(mm)
(mm)
(mm
Apparatus;
i. Keep the apparatus on the ground and apply grease on the inner surface of the
cylinders.
ii. Measure the mass by weighing the cylinder accurately and fix the cylinder on the
base in such a way that the central points of hoppers and cylinder lie on one vertical
line and cover the cylinder with a plate.
iii. For each 5 kg of aggregate mixes are to be prepared with water-cement ratio by
weight with 2.5 kg sand and 1.25 kg of cement and then add required amount of
water thoroughly until and unless concrete appears to be homogeneous.
iv. The concrete is placed in the upper hopper gently so that no effort is applied to produce
compaction.
v. The bottom door is opened so that the concrete falls on the lower hopper. Again the
bottom door of the lower hopper is opened and the concrete falls on the cylinder.
vi. After removing the excess concrete by the help of blades, the weight of the cylinder
(known volume) is taken to nearest 10 grams. This weight is known as ―weight of
partially compacted concrete‖.
vii. The cylinder is emptied and then filled with the same sample rammed heavily so as to
obtain full compaction. The cylinder is weighed to nearest 10 grams. This weight is
known as ―weight of fully compacted concrete‖.
Procedure
Step 1: Initially the sheet metal slump cone is placed inside the cylinder container that is placed
in the consistometer. The cone is filled with four layers of concrete. Each concrete layer is one
fourth the height of the cone. Each layer after pouring is subjected to twenty-five tamping with
the standard tamping rod. The tamping is done with the rounded end of the rod. The strokes are
distributed in uniform manner. This must be done in such a way that the strokes conducted for
the second and the subsequent layers of concrete must penetrate the bottom layers. Once the final
layer has been placed and compacted, the concrete is struck off to make it in level with the help
These are materials other than water, cement and aggregates which are added to concrete mix to
provide special properties to concrete. Admixtures are added in small amounts before or during
the mixing stage of the concrete production. The purpose of the admixtures is to improve on
certain properties of freshly laid or hardened concrete.
Functions of admixtures
Types of Admixtures
This accelerates strength development in cold weather. Calcium chloride (Cacl2) increases rate of
heat liberation during the first few hours. It also accelerates setting, it however, may corrode
reinforcements when used and it also reduces resistance of concrete to sulphate attack.
Hydrochloric acid (Hcl) also reduces the resistance of the concrete to sulphate attack.
ii. Retarders:
Retarders generally slow down the hardening of the concrete paste. They are useful during
concreting in hot weather, when the normal setting time is shortened by higher temperatures
examples are sugar solute, zinc salt etc.
They are added as a means by which the water content of the concrete can be reduced without
suffering a loss in workability. Example hydroxylated carbonylic acid and their salts.
These prevent the absorption of rain water into the concrete e.g in concrete flat roof. The used
materials are usually vegetable/mineral oils.
v. Pore fillers
9.1 Introduction
They are the only bulk materials which have high strength in tension-even lead, the softest of the
metals commonly used in building has a tensile strength substantially in excess of that ordinary
concrete.
Their high strength is also matched by high stiffness (modules of elasticity – there is reasonable
correlation between strength and stiffness because both are related to metallic bond strength.
STEEL
The presence of carbon in iron leads to the formation of a non-metallic compound, iron carbide.
This is intensely hard and brittle and exists as very fine sheets interwoven with iron sheets to
form a compound called pearlite. Pearlite causes plastic flow or yield to occur much less readily
then in pure iron which contains no pealite. However, the presence of too much pearlite reduces
ductility, toughness and weld ability.
Low carbon steels include steels referred to as mild steel and high yield steels. They form a very
large proportion of the steel used in construction. They have moderate strength, good toughness,
ductility and welding properties on account of the fairly low proportion of pearlite. Examples
include weldable structural steels, cold rolled steel sections.
In addition to containing some carbon, low carbon steel present as a result of other elements,
some present as a result of the manufacturing process and others included to benefit certain
properties of the steel.
i) Sulphur and phosphorous These form precipitates of iron sulphites (FeS) and
phosphide (Fe3P) respectively, which cause embrittlement. These are therefore
restricted to about 0.05% in mild steel.
ii) Silicon when present in small quantities, it dissolves in the iron, increasing strength.
Large quantities cause embrittlement and hence silicon is normally restricted to about
0.2%.
Manganese- This is useful because it increase the yield strength and hardness of low carbon
steels. It also increases hardenability and may combine with sulphur to reduce brittleness caused
by the sulphur.
Nobium- this tends to produce smaller crystals (grains) resulting in increased yield stress
quantities may be up to 0.04%.
All metals used for engineering purposes are classified into 2 categories
i) Aluminium
ii) Copper
iii) Zinc
iv) Lead
v) Tin etc
Iron is never found pure in nature, it has to be extracted in the form of pig iron from the various
iron ores e.g.
Pig iron is the crudest form of iron while wrought iron is the purest form of iron.
Pig iron forms the basic material for the manufacture of cast, iron, wrought iron and steel. It
contains 92-95% iron, 3-4% carbon and the remainders are impurities like sulphur, manganese,
phosphates etc.
The main use is as base material for the manufacture of cast iron, wrought iron and mild steel by
refining. Pig iron is not used for structural purposes.
Iron ores obtained from mines in the form of boulders are broken up and crushed to pieces of
about 2.5cm. After crushing, ores are generally washed in a stream of water to remove impurities
like clay, loam and other materials called gangue materials.
Perforated trays may be kept to remove sand and pebbles. Magnetic separators may be used in
dry conditions to remove impurities.
Dressed ores are heated in the presence of air. This is called calcinations and is done to oxidize
the iron ores. Water and carbon dioxide are driven out by this process.
Dressed ores may be roasted to make them hot dry. Roasting drives away sulphur and/or volatile
materials from the ore. If iron ores is an oxide, roasting may be avoided.
Dressed and calcined ores are melted in a furnace known as blast furnace. The metal is separated
by melting from ores. This is known as smelting.
The blast furnace is a tall irregularly shaped vertical steel cylinder. The outer shell is steel plate
30-40mm thick and inside is lined with a lining of fire bricks. The height of cylinder is about
30m and diameter between 6-10m.
A mixture of dressed iron ores, fluxing material and fuel (coke) are prepared in required
proportions and fed into the blast furnace through the top and these descend through the cylinder.
The oxygen in the hot air blast combines with carbon in the coke fuel to form carbon dioxide
(C02) which under intense heat is further reduced to carbon monoxide (CO). both carbon and
carbon monoxide act as reducing agents and reduce the iron ore to metallic state. Reduction of
the ore starts at the top and continues as the charge descents further and as temperature in the ore
starts at the top and continues as the charge descents further and as temperature in the furnace
goes on increasing. By the time the charge reaches the bottom, reduction of the iron ore is almost
completed.
The following are the reactions that take place inside the furnace
3 Fe203+C 2Fe3O4 + CO
Fe3O4+4C 3Fe + 4 CO
At the bottom of the furnace, a temperature of 15000C is maintained. The charge fed from the top
gets completely reduced by that time and molten iron is tapped from the bottom of the furnace.
Slag which is formed during reduction also collects at the bottom but floats over molten metal.
Slag is formed by reacting the fluxing material and impurities the ore.
Limestone is the fluxing material used and coke is widely used as fuel. Fluxing materials is the
material, which can easily be fused. It fuses with the impurities in the iron one to form slag.
Blast furnaces are usually connected to other steel works where the molten pig may be directly
fed for further processing/ purification to prepare other types of steels. Alternatively the pig iron
is poured into mould and allowed to cool and solidify.
Electric reduction process adopted when electricity is cheaply and amply available. Furnace is
heated by means of electricity.
Low shaft blast furnace. Blast of enriched oxygen is used instead of usual hot air. Reduction of
iron ore is achieved in comparatively short period and shorter stack height.
Sponge iron process. Iron is directly obtained from ore. Ore is reduced at temperature below the
melting point. The product is called sponge iron, which is a porous mass of reduced iron with
some slag in it.
Pig iron classified mainly according to the percentage of carbon present in it. The carbon present
in the pig iron is in the form of combined carbon as well as free carbon.
Combined carbon makes the metal hard and gives it a fine crystalline structure. Free carbon also
termed as graphite or uncombined carbon makes the metal soft and gives it a coarse grained
structure.
This iron is only for making casting and is known as cast iron.
It is obtained from pig iron, which is resmelted to secure proper grade and carbon content and is
casted or moulded into desired shape castings.
It consist of a cylindrical shell, made of thick iron plate whose inside is lined with refractory
bricks and the inside diameter is about 1m and height varies from 4-7m.
This furnace does not work continuously. A charge is put in the furnace, which is melted and
discharged into moulds. This completes one cycle of operation in a cupola furnace.
The furnace is provided with a side door near the top for admitting fresh charge. Hot air is blown
into the furnace from near the bottom. The furnace is again cleaned thoroughly before a new
charge is admitted.
Separate tapping holes are provided at suitable heights from the bottom of the furnace for
draining out the slag and molten iron. Fuel used is mostly coke.
The furnace is filled with an intimate mixture of pig iron, scrap iron, limestone and coke in form
of alternate layers of coke and mixture of pig iron and scrap iron with limestone. Limestone is
used as a fluxing agent. Scrap iron is added to improve the quality of the resulting cast iron and
bring about economy in the cost of production.
The furnace is charged, it is fired and blast air is blown in near the bottom of the furnace under
pressure. The air is not preheated and the impurities in pig iron are removed by oxidation. Cold
air gets heated in the furnace as combustion of coke takes place in the furnace. High
temperatures cause pig iron to melt. Limestone acts as a flux to combine with impurities in the
pig iron and separate them as slag, which floats above the molten iron.
The impurities or pig iron ore are removed to some extent and relatively pure iron is obtained in
molten stage from the bottom of the furnace. Molten iron is led into moulds and cast. Iron
castings are obtained after its solidification. Slag is drained from the top of the molten iron at
regular intervals and disposed off as either waste or used in the manufacturer of slag cement.
Sulphur renders Cast 1ron hard and brittle and causes rapid solidification. It also causes defects
like blow holes and sand holes. It should not exceed 0.1%
Phosphorous – increased amount of phosphorous increase fluidity and renders cast iron brittle.
When its amount exceeds 0.3%, the resulting cast iron loses toughness and workability. For very
delicate and thin castings, percentage can be varied between 1 to 1.5%.
Silicon combines with part of the iron and forms a solid mass. It also removes carbon to some
extent. If its amount is less than 2.5%, silicon ensures better casting decreased shrinkage and
makes Cast 1ron soft.
Manganese – it renders cast iron hard and brittle. Should be restricted to less than 0.75% or so.
Cast iron is used for castings, rainwater pipes, gutters, gratings, railings, cisterns, manhole covers
and balustrades. It is also used for supports of heavy machinery, carriage wheels and bedplates.
It is a basic material for the manufacturer of wrought iron and mild steel
Is considered one of the purest forms of iron. Contains about 0.05% of carbon and 2.32 – 2.45%
for the rest of impurities. It is obtained by (i) the pudding process and (ii) Ashton process.
It is used for making roofing sheets, rods, gas and water pipes, boiler tubes, plain and ornamental
iron work such as grilles, gates and railings, window guard gratings and electro magnetism. It is
used for the manufacture of hardened steel. Use of wrought iron is being replaced by mild steel.
9.8 STEEL
Iron containing carbon varies in carbon content. From 2% to 4% it is known as cast iron, and that
containing 0.25% to 1.5% is known as steel.
There are seven processes or methods by which steel by which steel can be manufactured i.e.
Bessemer process
Cementation process
Crucible process
Duplex process
L.D process
This process may be basis or acidic. Basic open hearth is mostly used
The hearth of this furnace is filled with molten pig iron received from cupola or blast furnace
This process is named after the furnace used; the Bessemer Converter
Through the hearth, the mixture catches fire and because of the shape of the roof, it attacks the
molten mass on the hearth. This produce intense heat and impurities are oxidized. After this,
ferro–manganese and other substances are added to improve the quality. Aluminum is also added
to refine the grain of the molten metal and deoxidise it. The hearth is again for a few minutes.
Mechanical treatment is given to steel ingots to convert them into market or commercial forms.
The main object of mechanical treatment is to improve the quality of the metal by forcing its
particles closer. This may be through hot working hot working or cold working.
In cold working, the steel is shaped at room temperature and in hot working; the metal is heated
to a temperature above its re-crystallization temperature and then shaped.
Hot working is the most common method of working the steel. The following operations are
involved.
Essential difference between steel and cast iron is in the amount of carbon content. Steel gets
harder and tougher with the increase in carbon content. Up to 1.5% carbon content, all the carbon
gets into chemical combination with iron. Beyond that point, not all the carbon combines with
steel and the rest exists as graphite. At this stage metal falls into the category of cast iron. For a
material to be classified as steel, there should be no free graphite in it‘s composition.
- Structure is granular
- Tougher and more elastic than mild steels
- Easier to harden and to temper (heat steel to an appropriate temperature to toughen and
strengthen)
- More difficult to forge and weld
- Can be permanently magnetized
- Comparatively stronger in compression than in tension or in shear
- Withstand shocks and vibration better
Uses
- Essentially low carbon steel with carbon content less than 0.15% also termed as high
strength steel. Because of increased tensile strength, lesser weight of steel is used
compared to mild steel for the same jobs, the structure is thus lighter.
Properties
Uses
- Mild steel or high tension steel is embedded as reinforcement in concrete to make good
that deficiency of the plain concrete.
- Round bars, deformed bars (twisted) or ribbed bars are extensively used for that purpose.
Conversion of metal into their oxides and other compounds by natural agencies is called
corrosion – corrosion is also referred to as rust.
Steels suffer from rusting difficulty to the maximum extent. Preventive measures for rusting are
cold tar painting, electroplating, enameling, tinplating etc.
Corrosion takes place due to the chemical or electro- chemical reactions by which the metal is
converted into an oxide, salt or some other compounds. The substance resulting out of corrosion
is known as rust. The corrosion indicates the deterioration resulting out of corrosion is known as
rust. The corrosion indicates the deterioration and loss of metal due to chemical attack. The
corrosion may be dry corrosion or wet corrosion.
Corrosion taking place in the absence of electrolytes is known as dry corrosion. Electrolyte is a
substance which dissociates into ions in solution or when substance which deteriorate into ions in
solution or when fused thus becoming electrically conducting. If the electrolyte causing
corrosion is an aqueous solution s of acid salt or alkali, it is known as wet corrosion.
Tarring – iron is dipped in hot coal or tar so that a thin film of it sticks to the surface protecting
it from rust and corrosion.
Painting – paints, usually lead paints are applied to the surface to be escorted
Enameling- Enamel consists of high grade bases like zinc oxide or lead oxide ground in oil or
varnish – they dry slowly leaving a hard tough and elastic film which is smooth and durable.
Surfaces are washable and not affected by acids, alkalis, gases or steam.
Galvanizing – Depositing a fire film of zinc on the iron/ steel surface is called galvanizing.
Surface to be galvanized is first cleaned of all foreign matter by washing in acid and then with
clean water.
Surface is dried and then dripped in molten zinc. The film of zinc deposited on the surface
protects it in the atmosphere. Removal of the zinc film by wear or scratches exposes the surface
again to rust and corrosion.
Sheradising – Surface to be treated is cleaned of all foreign matter by washing it with acid
solution then clean water. It is dried and then covered with zinc dust. It is enclosed in steel boxes
to be heated in a furnace under controlled temperature. Molten zinc spreads over the whole
surface and on cooling, forms a thin protective layer. Sheradising gives better protection than
galvanizing.
Tin plating- surface cleared with acid wash and them with clean water. Surface is dried and then
dipped in a bath of molten tin. A protective layer is left on drying.
Angles with slots at regular intervals. Made to various sizes,. Punched steel straps are also
available for joints by tightening bolts and nuts.
These are good for assembly of structural components, scaffolds, benches or storage racks. Can
be used in combination with plywood, hardboards etc. they help in reducing cuttings costs and
time.
Like iron, non- ferrous metals also carry an equal importance in the field of their application.
9.1 Aluminium
Aluminium does not occur in pure form but is extracted from bauxite (A1203H20)
The extraction process consists of two operations only. Purification of the bauxite ore and
Electrolysis of the purified bauxite to get aluminium at about 10000C. This is expensive process
rendering aluminium a very expensive material.
i. Pure aluminium is a very soft metal and has to be alloyed with other metals to make it
useful for structural purpose.
ii. It is highly ductile and malleable metal
iii. Its melting point is 6580C and S.G 2.7
iv. It is a very light metal and resists corrosion very effectively
v. It is very tough and has high tensile strength
vi. Its colour is silvery white with a high lustre
vii. It can be rolled into sheets
9.1.2 Uses
i) When alloyed with other metals, it is used for making piston, cylinders in aeroplane
engines.
ii) Used for making electric cables
iii) Used for making automobile bodies, utensils etc
iv) Alumimium paints are made from it
v) Used as a protective coating to structural steel work
vi) Used for making show cases, high class doors and windows, furniture etc.
vii) Used for making structural members (profiles) for light construction work.
9.2 Copper
This is extracted from copper pyrite ores (CuFeS2). This ore contains about 30% copper
9.2.1 Properties
9.2.2 Uses
9.3 Lead
This metal does not occur in free state. It is extracted from an ore called galena (Pbs)
Roasting
Smelting and
9.3.1 Properties
9.3.2 Uses
Lead is mostly well in the form of oxide like white lead, red lead
9.4 Zinc
This metal does not occur in the Free State in nature but is obtained from calamine ore ZnCO3
and zinc blend ore.
The process of manufacture of zinc consists of reduction of the Zinc ores to the Oxide form. Zinc
oxide is then heated to 20000F in an electric furnace and pure zinc is liberated in the form of
vapour, which is then condensed. The condensed zinc is taken out of the chamber in liquid form,
skimmed and poured into moulds to form slabs or cast into ingots. The solidified zinc obtained is
called spelts. Zinc may also be obtained by electrolytic refining.
9.4.1 Properties
9.4.2 Uses
9.5 Tin
The process of extraction consists of crushing, roasting and then smelting the ore to a
temperature about 10000C in a blast or reverberatory furnace. The crude tin obtained is further
refined by heating or electrolysis.
9.5.1 Properties
i. When a tin bar is bent – a peculiar sound occurs which is also known as cry of tin
ii. Tin is a silvery – white, lustrous and malleable metal
iii. Melting temperature is 2320C
iv. It becomes brittle when heated to a temperature of about 2000C
v. It is not affected by dry air or pure water
vi. Its S.G is 7.30.
9.5.2 Uses
These include
9.6.1 Gold (Au) – used in making coins, jewellery, and decoration of porcelain and in the
electrical field.
9.6.3 Platinum (pt) – generally used as an alloy with gold, iridium and iron to produce more
useful metals, used for making jewellery, pen-points, scientific instruments, surgical instruments,
standard weights and temperature recording devices.
9.6.4 Cobalt – used widely in the preparation of special alloy steels, ceramic products and TV
articles.
9.6.6 Cadmium – pure metal carries very little application in industry but is used mostly in
alloyed form only.
9.6.7 Nickel (NI) – used widely as a protective coating on other metals also used in coins of
small denomination. Used is a variety of extremely important ferrous as well as non-ferrous
alloys.
9.6.8 Magnesium (Mg) – used in flash light photography fireworks and signaling purpose in the
army. In its pure form cannot be used for any engineering purposes but its alloy with other metal
are quite important.
9.6.9 Manganese (Mn) – used extensively in the manufacture of steel to act as a reducing agent.
It is added as an alloying element in steel to improve its strength, toughness and heat treatment
characteristics. Practically all commercial grades of steel contain manganese. It is also used in
electric batteries, paints and varnishes, staining agent etc.
9.7.1 Soldering – Parts of the metal to be joined are heated and an alloy (solder) (an alloy of lead
and tin) having its melting point lower than that of the parts to be soldered is applied over the
junction in the molten state.
9.7.2 Brazing – It adheres to the surfaces to be joined. It has poor tensile strength and serves
only to fill up the joint. Is similar to the operation of soldering but is done at a much higher
temperature (6000C – 11000C). It consists of a mixture of 1 part tin, 3 parts Zinc and 4 parts
copper. The blazing solder is applied to the joint in the presence of borax which acts as a flux.
The surface to be joined are held pressed firmly together until the brazing solder applied has
solidified. It is used in joining together iron, copper, brass etc.
9.7.3 Welding – is the process of joining metal to surfaces by the application of heat. The heat
for welding may be obtained by an electric ore, a gas flame or some chemical reaction.
9.1 Introduction
Plastics are available in market in a variety of forms to suit varied requirements. It is findings
newer usages in building construction and is just replacing many constructional materials like
timber and steel. It is being used to make fittings and fixtures to meet aesthetic requirements and
structural components to withstand wear and tear.
Shortage of conventional construction materials during the 2nd World War gave impetus to the
use of plastics in electrical and sanitary fittings like electric points, switches, holders, insulators,
cistern floats, W.C seats and domestic furniture.
Plastics are generally taken to imply a group of organic materials that become plastic on heating,
that they could be moulded to required shapes and on cooling down to normal temperatures
become rigid.
The term organic traditionally refers to materials which are derived from living materials e.g
timber, leather, cotton, wool but the term has come to be used for a wider range of materials
which in common with the above have properties dependant to a large degree on the presence of
carbon in their structural, therefore plastics, paints, adhesives, mastics and bitumen fall into this
larger group.
While traditional organic materials in the construction industry continue to be used at a steady
rate others such as plastics have enjoyed a spectacular rise in application and this trend is likely
to continue.
Plastics offer the advantage of low density, good resistance to the environment compared with
competitive materials and many forms require no maintenance in the short term.
The major problem of plastics is low stiffness and virtually all forms are combustible if not
flammable.
In energy terms, plastics may look expensive and subject to uncertainties arising from oil prices
fluctuations however, when their low density is considered, they become much more attractive.
Plastics – are natural or synthetic in origin. Natural plastics are found in cellulose, starch
compounds, in rubber latex and in natural resins e.g. shellac, copal, and rosin.
Cellulose – is the substance which forms the main structure of the cell walls of plants and to a
pol of glucose. For commercial use, it is obtained from the cotton plant, which is the purest
source, wood and straw. It is chemically classified as a carbohydrate.
Starch – is based on the glucose monomer and is present in plants as a as source of nutrients.
Proteins – are a group of organic nitrogenous components in polymerized form which make up
the structure of all plant and animal tissue. They are based on monomers of certain amino acids
sources of proteins; important in the early days if the plastic industry are casein (from milk) and
the bean.
Copal, rosin and rubber latex – are extracts of certain species of trees and Shellac is an
extractive certain insects.
All these naturally occurring polymers; cellulose, starch, proteins, rubber latex and resins have
which are called straight chain or linear molecular construction i.e the monomers are linked end
to end in a sit row. The polymer is simply made up of a series of these chains lying together with
their length parallel to a common axis but with their ends over lapping.
Plastics are organic substances prepared from natural or synthetic resins in which other materials
like fillers, solvents, plasticizers might have been added or not. In general terms, plastics may be
stated by compounds of carbon with other elements such as oxygen, hydrogen, nitrogen. Other
ingredients apart from the monomer base, which can be incorporated during the manufacture of
plastics to serve as some specific purpose are;-
Solvents – These give the material more plasticity during the manufacturing stage, usually to
facilitate moulding to the desired shape e.g acetone and chloroform.
Plasticisers – These are usually non-volatile organic solvents of high boiling point, added to
reduce brittleness and increase flexibility of the finished plastic material.
Fillers – these are added to modify one or more properties of the finished plastics materials e.g
reinforcing agent like glass fibre to improve strength, or wood flour to improve toughness or
asbestos confer heat resistance. Others are finely divided materials like china clay, talc added to
reduce wear and cost.
Catalysts – e.g either are used to assist and accelerate hardening of the plastic. They help in
quick and complete polymerization.
Pigments – These impart the desired colour of the plastics besides acting as filler e.g Zinc oxide
barytes.
Stabilizer – these interfere with thermal oxidation and slow down the degradation of plastics
during processing and use.
Lubricant – these are used on the surface of moulds to prevent plastics materials sticking to the
mould e.g graphite paraffin wax, etc.
i) Thermosetting plastics
ii) Thermoplastics.
These set into permanent shape when heat and pressure are applied to them. Once formed, they
can be re-softened by heat. These plastics have giant three dimensional molecules and cannot be
softened by heat. Therefore, the shape must be prepared prior to polymerization. The typical
molecules arrangement of the thermosetting plastic is with the monomers arranged to form a 2 or
3 dimension grid like structure with chains cross-linked.
Thermosetting plastics are soluble in alcohol and certain organic solvents when they are in the
thermosetting plastic stage. They have high strength and are insoluble in many organic solvents
such as benzene and acetone once formed. Examples are phenolformaldehyde,
ureaformaldehyde, polyester resins and epoxy resins. This property is utilized for making paints
and vanishes from these plastics. These plastics are strong, hard, durable and available in many
colours.
In general, thermosetting plastics are more heat stable and more resistant to solvent action than
thermoplastics.
9.4.2 Thermoplastics
Thermoplastics have long-chain molecules linked by weak electrostatic forces known as van der
weals forces. These forces weaken further on heating to softening as the distance between
molecules increase with small rises in temperatures hence the plastics exhibit substantial thermal
movement, e.g polyethylene (polythene), polyvinyl chloride, polystyrene, acrylic resins, nylon
and polytetra fluo ethylene.
Thermoplastics become soft when heated and harden when cooled regardless of the number of
times the process is repeated. The process of softening and hardening may be repeated for an
indefinite number of times. These plastics are thermoplastic because they are sensitive to heat
(i) Rigid plastic – Have high modules of elasticity, maintain their shape under external
stress normal as well as increased temperatures.
(ii) Semi-rigid plastics – Have medium modules of elasticity. Elongation under pressure
completely disappears when pressure removed.
(iii) Soft plastics – These have low modules of elasticity. Elongation under pressure
disappears slowly on removal of pressure.
(iv) Elastomers – These have soft and plastic materials having very low modules of
elasticity. The deform considerably under load and return to the original shape on
removal of the load Elongation can range up to 10 times their original dimensions.
Majority of plastics in everyday use are made from derivatives of coal tar, mineral oil
(petroleum) and natural gasses.
9.7 Properties
Plastics with a wide range of different properties are available. In general, plastics are;-
The method chosen depends upon the type of plastic i.e thermoplastics or thermosetting plastics
and shape of the finished product.
1. Blowing – Thermoplastic material is softened and then blown by air or steam into a
closed mould e.g jars, bottles, toys are casted by this method.
2. Casting – Molten plastic is poured into moulds which are normally made of lead. The
plastic cured at 700C for several days. During curing, low pressure may be applied if
necessary. The method is most suitable for cellulose plastics.
3. Calendering – Plastics material is made to pass through cylinders. 4 sets are kept heated
and last one kept cold. While passing through the first 3 sets, the plastic is turned into
thin sheets. Cooled while passing through the fourth cylinder. Some drums may be
provided with artistic des,,,, to reflect them on the finished product. If cloth is to be given
plastic coating, it is inserted along plastic material between the second and third heated
rollers.
4. Laminating – This processes is adopted in case of thermosetting plastics. Paper sheets,
asbestos are applied with this plastic to form plastic laminates. Thickness of sheets varies
from 0.12mm – 15mm. They possess excellent mechanical and electrical properties.
Due to the pleasing finished surface, they are used for ornamental and decorative
purposes.
5. Moulding – is the most common method for the fabrication of plastic articles. The
following are some of the commonly adopted moulding processes.
i. Compression moulding – This is the most widely used method of moulding and
is used for both thermosetting and thermoplastics. The moulds are preheated; the
plastic material is put in preheated moulds and the moulds are closed. 300 kg/cm.
(i) Most plastics cannot be used at higher temperatures. Thermoplastics generally cannot be
used above 1000C and thermosets above 1500C.
(ii) Most plastics possess low resistance.
(iii)They are not very hard.
(iv) Exhibit high creep.
(v) They have high coefficients of thermal expansion.
(i) Flooring: - thermoplastics or polyvinyl (PVC or PVA) are used for flooring in form of
sheets and tiles. Polyvinyl Chloride (PVC) is resistant to abrasion and is unaffected by
many chemicals.
(iii) Pipes:- plastic pipes are finding more and more usage in water supply, sanitation and
specialized industrial applications. Polythene and PVC pipes are the most extensively
used ones. Plastic pipes are excellent in use at low temperatures; they are ductile and can
be threaded.
(v) Concrete shuttering:- The moulds and forms of fibre reinforced plastic (FRP) give
concrete shapes of very high quality, very complicated concrete shapes can be moulded
in.
(vi) Other uses include doors and window frames, internal partitions and wall panelling,
structural sections, temporary shelters, water storage tanks, furniture items, polymer
membranes, polymers in civil engineering.
General
Painting is the application of a thin coating of material in a liquid as plastic condition to a surface
as a decorative or protective measure. The applied coating is normally required to dry out or
harden to form a solid film.
The coating applied can vary widely in its composition and chemical and physical proportions
depending on the:
Method of application
Materials used are of different classes such as paints, vanishes, stains, and preservatives.
In the early days of the craft, the painter mixed his own materials, the exact ingredients and their
proportions being to a certain extent trade secrets. Eventually, there appeared on the market the
ready mixed products made by specialist manufacturers to proprietary formulations or to the
larger customers specifications.
Simple classification of paints is difficult because of the range of products now available is so
vast. It is therefore important to take the manufacturer‘s instructions and recommendations
regarding selections, storage, preparation, application, subsequent treatment and maintenance of
their product seriously.
Functions of paints
Provide a protective layer on the material covered by excluding the atmosphere moisture,
chemical, fungi, and insects.
PAINT SYSTEM
Adequate preparation of the surface to be painted is very essential for success. The surface
should be smooth (not shiny for this would not give an adequate key), clean, dry and stable.
The paint film is built up with more than one coat i.e. priming coat, undercoat and a finishing
coat. The selection of a suitable type of each of these coats depends on the material of the surface
and its location (internal or external)
Each coat must be dry, hard and rubbed down with fine abrasive paper before the next is added.
Priming coat-this is the first layer of paint. It must suit the background and adhere to it and it
must be compatible with subsequent layers.
i. Give protection against corrosion of metals or against dampness, especially of site stored
joinery.
There are different types of primers for metals; timber and cement/lime plaster surfaces.
Undercoats
Undercoats tend to be heavily pigmented and usually need to be sealed against the weather by a
finishing coat.
Finishing coat
i. Gives the required characteristics to the painted surface (flat, eggshell or high gloss)
ii. Also gives the final colour
iii. In the case of exterior paints, finishing paints must also seal off the surface against the
weather and some elasticity may be desired
CONSTITUENTS OF PAINTS;
I. Base
The vehicle or medium is the liquid part of the paint. Its primary function is to:
Pigments are usually present in powder form in suspension in the vehicle; their function is to
provide the capacity (hiding power), colour of the paint film, to confer durability or corrosion
resistance to the surface painted or both. Pigments are in the main inert, white or coloured
powders e.g. metallic oxides or salts. They may sometimes have a chemical influence in the
hardening of the paint film. They are obtainable in powder form or are sometimes mixed with oil
or as a paste
Natural white pigments are barytes (barium sulphate), whiting or Paris white (chalk),
china clay or kaolin, terra alba or gypsum(calcium sulphate).Artificial white pigment
includes white lead(carbonate and hydroxide of lead), titanium oxide, zinc white (zinc
oxide) and antimony white (antimony oxide). In general, artificial whites give better
opacity than the natural whites.
Pigments of low opacity may be added to high opacity pigments to impart some other
desirable property e.g. make application easier, or assist suspension of the solid particles
in which case they are referred to as an extenders.
Black pigments include, carbon black, lampblack, vegetable black and all forms of
carbon obtained by burning organic matter in a restricted supply of air or oxygen.
The function of the thinners is to reduce consistency of the paint so that it can be easily applied
on the surface-it evaporates after the paint has been applied to the surface. It also helps the paint
to penetrate in to the surface to be painted.
A volatile solvent is a liquid which dissolves a substance (the film forming substance) but which
readily evaporates, leaving behind the dissolved substances unaltered chemically; these include
alcohols e.g. methylated spirit, naphthas and other coal far derivatives and other organic
chemicals.
A resin-is either a natural extract from certain trees e.g. copal or insects (shellac) or material
similar in character but synthetic in origin.
V. Driers
Are added in oil bound paints-these are usually oxides which will give out oxygen and thereby
increase the rate of oxidation of the binder and the rate of drying.
Fungicides and insecticides added to prevent attack by insects and to prevent formation of
moulds.
Oil vanish is a substantially transparent, pigment free composition of drying oils, natural or
synthetic resins and solvents.
Drying oil is an oil which has the property of hardening to a paint film when exposed to the
atmosphere wholly or partly by chemical action with absorbed oxygen. Dry oils may be natural
extract or synthetic and are mainly vegetable extracts such as linseed oil from the seed of the flux
plant, Tung oil from the seeds of certain trees and soya bean oil. These oils have to be processed
in such a way that their natural drying times are considerably reduced.
Extender-used to improve some of the properties of the paint, although they have little or no
pigmentary value and can be used to control amount of glows; addition of suitable filler can
considerably reduce cost and sometimes improve viscosity. Finish extenders can be up to 45%
and their particles are much larger than pigment particles.
TYPES OF PAINT
These were traditionally based on white lead dispersed in linseed oil medium (obtained from flax
plants) or Tung oil (obtained from soya beans). Oil paints dry by evaporation of the solvent and
by oxidation. Once hardened, oil based paint behave as thermosetting plastics, being resistant to
solution in the oils from which they were formed. Such paints form films in the can unless a
protective coating of say white spirit is applied. These take a very long time to dry, 3-12 hours
depending on temperature and humidity.
b) Synthetic paints
c) Water paints
These are also known as distempers and are mainly used in internal walls and ceilings. There are
several kinds and are prepared on site by adding water to a paste. They have a dry oil or varnish
medium emulsified in water containing glue or other derivatives.
The cheapest type is known as soft or ceiling distemper which contains only glue vehicle and
tinted powder chalk. Can be removed by washing or brushing and so is only used for ceilings.
Oil bound distemper is a better quality having a mixture of linseed oil pigment and extender. It
will withstand limited careful washing. Emulsion paint has superseded water paint. Another
types are cement types, often used externally. They contain white or coloured Portland cement
with a waterproof, accelerator and extender.
d) Emulsion paints
Emulsion paint has the pigments and the medium dispersed as small globules in water. Oil,
synthetic resin and bitumen are common mediums. Among the different emulsion paints are
alkyd, bitumen, and polyvinyl acetate and styrene emulsions. They are mainly used on wall
surfaces. Oil bound distemper in (c) above is a type of emulsion paint.
Finishes are usually `matt` (dull), `silk, or satin, thought some gloss paints are now available.
Drying times vary according to conditions-could be as low as one hour in a warm dry well
ventilated enclosure. In cold, damp conditions, they may take a very long time to set or fail to set
at all
Hardened film is fairly permeable, hence the paints can be applied to slightly damp
materials (e.g. new plaster) permitting subsequent drying of the background.
PVA emulsions are alkali resistant hence can be used on cement backgrounds subject to
some dampness.
Can be used externally. Lifetime is 4-7 years depending on quality
e) Cellulose paints
These are synthetically produced from cellulose compounds and most of them have to be applied
as a spray for they dry quickly by evaporation of the solvent. For example nitrocellulose is
produced by the action of nitric acid and sulphuric acid on a form of cellulose such as wood
pulp. It is highly explosive and dampers are added. The volatile material will be 70-80% of the
total, consisting of about seven different hydrocarbons. It forms a rapid drying paint suited to
such applications as spraying of motorcars and other manufactured items. A part from some
kinds containing metal powders (aluminium and bronze) they are not satisfactory for general
building work.
f) Varnishes
These are of two kinds, oil varnish and spirit varnish. They are used to give a transparent film to
surface. Oil varnish contains linseed oil or other drying oils, driers, synthetic or natural resins
and solvents. They dry by evaporation of the solvent and oxidation of the oil.
Spirit varnishes are solutions of shellac and other spirit resins dissolved in commercial alcohol.
g) Special paints
These include aluminium paint, anti-condensation paint, bituminous paint (the vehicle for this is
mainly bitumen and it provides a cheap method of protecting steel where appearance is
secondary) chlorinated rubber paint, fire resistance paints (these are used to increase the
a. Ferrous metals
The best time to paint steel is immediately after production though mill scale (iron oxide
produced during rolling) should be removed because it may lead to local corrosion and
may eventually flake off due to differential movement.
Corrosion should be removed either by sand papering or grit blasting or pickling
(treatment with hydrochloric/phosphoric acid).
Suitable primers, include red lead (lead oxide), zinc dust, zinc chromate and zinc
phosphate. On account of their toxicity, lead-based primers are not recommended for
used in domestic situations.
Afterwards, a decorative finish may be applied. Undercoats may or may not be excluded.
Generally, the more aggressive the environment the more coats should be given.
e. Plastics
The surface must be roughened first to give a mechanical key, and then afterwards painted.
Any paint film applied to damp materials and which is not appreciably permeably will
likely fail by softening, blistering, peeling, or flaking.
If the background is of an alkaline nature, the presence of moisture can cause bleaching
of certain pigments and softening of an oil bound film due to chemical action, with an
eventual break down. The softening action is known as alkali attack or saponification.
When an acid and an alkali react together, the result is a soap and water. This is known as
saponification. Lime mortars and plasters, Portland cement and asbestos cement develop
alkalis, especially when new. If such surfaces are coated with an oil-bound paint,
particularly in the presence of even small quantities of moisture, they will cause
saponification. The paint may blister in a mild attack or show yellow soapy runs in a
severe attack. The problem can be avoided by (i) allowing the background to dry
completely before printing (ii) by use of alkali resistant primers (iii) use of PVA emulsion
paints instead of oil based points.
Where soluble salts are present in the background materials, dampness can lead to their
crystallisation beneath a paint film which is not substantially permeable and can cause
unsightly efflorescence on the surface of permeable films.
Moulds can grow in damp conditions causing stains where a food source is available
such as carbohydrates (e.g. sapwood). These can be prevented by the use of antiseptic
solutions and eliminating the source of dampness.
This may be due to normal form of deterioration due to weathering or unsuitable paint
formulation, adulteration, wrong selection or application techniques or subsequent maltreatment.
(iv) Chalking
This describes erosion of paint film due to inadequate binder performance. It is caused by use of
paints containing either a poor quality binder or inadequate quantity of binder.
(iv) Bleaching
This result from the softening of a paint film due to an agency such as resinous or bituminous
matter acting as solvent on the binders. The solvent gradually penetrates the paint film and
causes staining and local break down (e.g. break down of an oil or resin film on timber due to
resin exuded from knots).
This can be prevented by the use of a suitable sealer as a barrier coat e.g. shellac` knotting`
applied to knots in timber or leafing aluminium paint on bitumen –coated surfaces.
(v) Sulphiding
This is the discolouration of certain paint films due to the conversion of compounds present to
the sulphide e.g. blackening of lead based paints due to lead sulphide formed by the action of
sulphurous fumes in an industrial atmosphere.
STORAGE OF PAINTS
Most paints are mixtures and their constituents are liable to separate out to form different layers
during storage. Thorough remixing should therefore be done before and during use.
Where skin form at the surface, it will usually re-dissolve on mixing in solvent paints. For non-
solvent paints, it should be removed by straining the paint through a fine –mesh fabric.
Hardness test
Drying test
Abrasion and alkalis resistance test
Bituminous materials are extensively used for roadway construction, primarily because of their
excellent binding characteristics, water proofing properties and relatively low cost. Bituminous
materials include: Bitumen, Asphalt and Tar.
Bituminous materials are being extensively used in damp proofing the basements, floors, roofs,
damp proof courses; painting timber and steel structural elements; as adhesives and caulking
compounds, and tars are used as binders in road works. When combined with aggregate these are
also used to provide floor surfaces. Bitumen is now more commonly used for building purposes
than is tar.
1) BITUMEN
It is the building materials in which it is obtained by the fractional distillation from crude
petroleum oils as an end product.
Bitumen is a noncrystalline solid or viscous material derived from petroleum, by natural or
refinery process and substantially soluble in carbon disulphide. It is asphalt in solid state and
mineral tar in semi fluid state. Bitumen is brown or black in colour.
The main constituent is petrolene a yellowish oily substance, an excess of which makes bitumen
to melt at low temperature and, asphaltene—hard black substance, an excess of which makes
bitumen brittle and non-plastic.
FORMS OF BITUMEN
Bitumen Emulsion is a liquid product containing bitumen to a great extent in an aqueous
medium. The bitumen which is in a very finely divided state (globules of about 2 micron
diameter) is kept suspended in the aqueous medium with the help of some suitable stabilizing
agents. Depending upon the stability of the protective coating of the emulsifying agent, the
emulsions are classed as rapid setting (RS), medium setting (MS) and slow setting (SS). These
emulsions are always stored in air tight drums.
Blown Bitumen is obtained by passing air under pressure at a higher temperature through
the bitumen. It can be used as roofing and damp-proofing felts, in the manufacture of pipe
asphalts and joint fillers, as heat insulating material, etc.
CLASSIFICATION OF BITUMEN
Natural Bitumen: Pure natural bitumen occurs rarely. Lime stones, sandstones and soils
impregnated with bitumen are frequently found. It originates from the accumulation of petroleum
in the top layers of earth crust through migration, filling pores and cavities of rocks, under the
action of high temperature and pressure. The natural bitumen is dark-brown in colour which on
heating gradually softens and passes to liquid state and on cooling solidifies. It is insoluble in
water but dissolves in carbon disulphide, chloroform, benzene and very little in gasoline. Natural
bitumen may be extracted from bituminous rocks by blowing in kettles or dissolving in organic
solvents (extraction).
Petroleum Bitumens are product of processing crude petroleum and its resinous residues.
These are classified as residual asphaltums, oxidized, cracked and extracted bitumens.
(ii) Based on consistency These are classified as solid, semi-solid and liquid bitumens.
(iii)Based on application Bitumens are classified as road construction bitumen, building
bitumen and roofing bitumen.
2) TAR
It is a dark (deep black) viscous liquid produced by destructive distillation of organic material
such as coal, oil, lignite and wool. Depending upon the source of origin it is classified as coal tar,
wood tar and mineral tar. Tar is restraint to petroleum-based solvents. It has very low bitumen
content.
Coal Tar: is obtained, as a byproduct in the destructive distillation of coal, or in the manufacture
of coal gas. It is heavy, strong smelling and black. These generally have high specific gravities
and viscosities, and good adhesive properties. On the further distillation of coal tar (from coal
Wood Tar is obtained by the destructive distillation of resinous wood (pine, etc.). It contains
creosote and as such is a very strong preservative. On further distillation wood tar produces
wood creosote. Compared to coal tar creosote, it is an inferior preservative for wood. The residue
left after the distillation is known as pitch. There are five grades of road tars:
RT-1: For surface painting under exceptionally cold weather conditions, hill roads at very high
elevations.
RT-2: For standard surface painting under normal climatic conditions.
RT-3: For surface painting and renewal coats and is also used for premixing chips in top courses.
RT-4: For premixing tar macadam (base course).
RT-5: For grouting.
Mineral Tar is obtained by the distillation of bituminous shales. Some examples are tarmac, tar
paving and tar macadam.
Tarmac is ironstone slag impregnated with tar oils. It is impervious to water and used in road
pavement.
Tar paving is a composition of limestone and coaltar. It is heated before use.
Tar Macadam is used for road pavement. Soft rock materials such as limestones blast furnance
cinder, etc. are heated in a furnace and then mixed with boiling coal tar, pitch and creosote oil.
The mix is applied in road soon after cooling and rolled.
PROPERTIES OF TAR
(i) It is more adhesive
(ii) It is less durable
(iii)It is harden quickly
(iv) Its setting time is more
(v) It contains high percentage of carbon
USES OF TAR
ENGINEERING MATERIALS & CONCRETE TECHNOLOGY
Page 224
(i) It is used in road constructions
(ii) It is also used for preserving woods/timbers
(iii)It is also used for filling leakages or cracks
(iv) It is also used for making paints
3) ASPHALT
Asphalt is a natural or artificial mixture in which bitumen is associated with inert mineral matter.
It is black or brownish black in colour. At temperature between 50–100°C it is in liquid state
whereas at temperature less than this it remains in solid state. Because it is a thermoplastic
material it softens as it is heated and hardens as it is cooled. It is the basic paving material in
use today.
Mastic Asphalt is also known as native asphalt. When obtained from lakes it is termed as lake
asphalt. It is used for making pavements, for water proofing of structure, stopping vibrations in
machine foundations, tunnels and subways, in manufacture of marine glue, and in lining
trenches.
PROPERTIES OF ASPHALT
(i) It is water proof and easily cleaned
(ii) It is durable and tough material
(iii)It is resilient and elastic in nature
(iv) It is good insulator of electricity, heat and sound
(v) It is good water resistance
(vi) It is not affected by certain chemicals
(vii) It is corrosion resistance
USES OF ASPHALT
13.1 General
Glass as a glazing material has remained unchallenged and seems likely to dominate this
field into the foreseable future because;-
Ordinary glass is based on silica (silicon dioxide) which is crystalline form, exists in a tetrahedral
array. If molten silica is cooled at normal rates from the liquid, an amorphous structure results,
which may be regarded as a heavily and randomly distorted form of the crystalline structure.
Silica, though forming the basis network of glass, is not used in the pure form because its
melting point is too high (about 17000C). Therefore, silica is modified by compounds such as
sodium carbonate. At high temperatures, sodium carbonate decomposes into sodium oxide, and
combines with some of the silica to form sodium disilicate. These chemical reactions disrupt
some of the rigid silicon-oxygen links. ‗Soda-glass‘ as the material is known, melts at a much
lower temperature, about 8000C. Soda glass is water soluble therefore, calcium carbonate is
added to stabilize the glass. Approximate composition of raw materials for typical soda – lime
glass is;-
PRINCIPAL CONSTITUENTS
Glass is obtained by fusion of silica, chalk (lime), potash, soda at over 1000oC. Functions of
the various important constituents of glass are;
1) Silica. It is the main constituent of all kinds of glass. Since it fuses at very high
temperatures some alkaline admixture like sodium carbonate or potassium carbonate
is added to it so as to make it fuse at lower temperatures.
2) Potash. This renders glass infusible and gives fire resisting properties to it.
3) Soda. It quickens fusion of glass and as such excess of it is harmful.
4) Lime. It imparts durability and toughness to glass
5) Lead oxide. It gives colour to glass and therefore its presence in glass is not much
desirable
6) Cullet. It is broken glass of the type desired to be manufactured that I added to the
raw materials to bring down the cost of production.
(i) Melting
(ii) Forming
(iii) Cooling
(iv) Finishing.
Raw materials are weighed and mixed in the correct proportions producing a mixture known as
frit. Waste broken glass ‗cullet‘ is recycled along with frit, usually the proportions of 80% frit
and 20% cullet. The mixture is heated to about 1500oC. The cullet melts first and permits
reaction and fusion of the remaining ingredients at temperature below melting point of pure
silica. The liquid is then cooled to a temperature of 10000C – 12000C where its viscosity is
sufficiently high for forming.
The final cooling shape after hardening must be gradual to prevent cracking and is referred to as
annealing.
Variations in the detailed procedure of manufacture and inclusion of special ingredients results in
different types of glass.
Classification of Glass
It is obtained from the fusion of a mixture of silica, lime, soda and alumina. Powdered glass too
may be added. This glass is also termed as soda ash glass, soda glass or soft glass.
It is used for glazing doors, windows and for making ordinary glass wares.
2) Lead glass
It is obtained from the fusion of a mixture of silica, lead and potash. Powdered glass too may be
added. This glass is also termed as flint glass.
Lead glass has highly shining appearance and takes good polish.
It is not affected by temperature. Cut glass work, electric bulbs and optical glass are made from
it.
3) Boro-silicate glass
It is obtained from the fusion of silica borax, lime and feldspar. Powdered glass too may be
added. This glass withstands high temperatures and as such laboratory equipment and cooking
utensils are made out of it.
Glass is marketed in various commercial forms to suit varying field requirements. Some
important commercial forms of glass are discussed below;
As the name suggests, this is made using the float process. The width is usually up to 1m and
length is limited only by handling considerations.
Molten glass is floated onto the surface of molten tin, and then allowed to cool. This produces
glass having flat parallel surfaces and the fire-finish associated with drawn sheet glass. This glass
is now used for general glazing purposes as well as mirrors, shop windows and in situation
where clear, undistorted vision is essential.
This type is dying out and is being replaced by float glass as new plants come on stream. The
surface is more variable than that of float glass. Normally graded into the following;-
OQ - Ordinary Quality
Viscous liquid glass at around 1000 – 12000C is drawn vertically to form a continuous sheet
passing through asbestos covered rollers (to prevent wasting) by iron grille bait dipped into the
molten glass and then slowly raised.
The sheet rises up to 9m, passing through a tower of water cooled chambers where it is annealed.
In emerging at the top, it is cut to the required length and trimmed. The surfaces of the glass are
never perfectly flat, resulting in slight distortion of vision but have a characteristic brilliance
known as a ‗fire finish‘.
The glass was formerly used in domestic dwelling, offices and factories.
This covers all glasses which are passed between rollers to give a specific surface finish whether
regular pattern or random diffusing surface. They are usually used where privacy or diffusion is
required or where specific decoration effects are required.
This method is principally used in the production of figured glass – that is where one or both
surfaces are textured or impressed with a pattern, which prevents clear vision through the glass.
In the original process, molten glass was poured a sheet of the required thickness. Any pattern on
the roller is impressed in the surface of the glass. The more recent system is to draw a sheet
horizontally between double rollers. Types of glass made by this method includes those known
as rolled, figured rolled, rough cast, cathedral and wired.
Though not specifically classified as a true safety glass, the presence of wires hold the glass
fragments together when breakage occurs in the event of bodily impact. However, the main use
of wired glass is to create fire resistant glazing systems.
Body coloured and tinted glass are produced by varying the constituents in the melting furnace.
The colour is present throughout the thickness of the glass. Different thickness of the same mix
will have different light and solar energy transmissions. Thicker glass will appear more strongly
coloured.
Body coloured/tinted glass are used either as solar control glasses where changes to the glass
composition increase the absorption, thus reducing the amount of light and total solar energy
transmitted. So called tinted glasses are used partly for decorative purposes.
(i) Coated glass – thin coatings are applied to large areas of flat glass. Coatings are applied
to alter the performance of the basic float glass that is light and radiant heat transmission,
light and radiant heat reflections and surface emissivity coatings have been developed to
have high transparency but high reflectivity of long wave radiation (low emissivity
coatings) to improve the thermal insulation properties of the treated glass.
More than one coating can be applied to the glass surface to give particular properties.
(ii) Toughened glass – The technique creates a state of high compressions in the outer
surfaces of the glass. Although most other characteristics remain unchanged, the tensile
strength is usually increased by 4-5 times that of annealed glass.
When broken, the toughened glass fractures into relatively small pieces usually in the form of
small cubes. The lengths of the cubes are normally the same as the thickness of the glass. These
cubes do not have the sharp blade-like edges and dagger points of broken annealed glass. Hence
it is regarded as a safety glazing material in the various codes of practice and standards.
All float and sheet glasses can be toughened. Wired glass cannot be satisfactorily toughened.
The glasses which are toughened must be cut to size; otherwise any attempt to work the glass
after toughening will cause the glass to shatter.
Toughened glass is usually used there a safe breaking pattern is required rather than for
additional strength.
(iii) Laminated glass
This is produced by bonding two glasses together with a plastic material or a resin. The layer,
which is usually polyvinyl butyral, can be either clear or tinted. The bonding is achieved by
heating the glass/interlayer sandwich and applying pressure.
Silvering is a chemical process normally used to create mirrors by depositing a layer of metallic
silver onto the surface of a piece of clear glass. The silver deposit usually protected by a layer of
copper which in turn is protected by a special paint coating. The silver surface is viewed through
the glass.
For special surfaces, front silvered mirrors can be produced. These have the reflective material
on the front surface of the glass.
13.3.8 Bent glass
This can be produced by heating most basic glasses to the point where they soften until they can
either be pressed or sag bent over suitable formers. Bent can be created in two planes.
This incorporates two or more glasses separated by spaces to create a cavity between successive
panes to form a unit. These are attached by suitable adhensive. Cavities range from 5-20mm.
These are made in a variety of patterns, sizes, colours and degrees of transparency. These units
are laid in a manner similar to that for normal building bricks using fine sand, lime; cement
mortar.
These can provide up to 60 min of stability/integrity when correctly formed. The following
approaches are relevant to increasing fire resistant;-
Glazing used in a structural manner must have the appropriate specifications, thickness and
bedding techniques to resist the applied forces. Loads to be resisted can be obtained from BS
6395: Loading for Building part 2: Code of Practice for Wing Loading.
Systems have been designed in such a way as to allow toughened glass plates to be assembled to
create continuous glass facades without the use of mullions and transoms.
The plates are usually bolted together using special metal patch fitting at their corners.
Edge finishes (flat ground, round beveled or bull nosed) may be achieved by grinding and
polishing.
Water jet cutters may be used to achieve holes and irregular shapes.