Metal Processing
Metal Processing
(AS852-CO2)
Lecture : 3 H/W Year: I
Practical :1/3 H/W Part: II
Course Objectives:
Objectives of the course is to provide the knowledge on basic principles of materials processing and their applications for
materials characterization.
Course Contents:
I. Processing of metals [8 Hrs.]
1.1 Solidification nucleation, crystal growth, grain structure, solidification defects (shrinkage, gas porosity) concept of
solidification of metals, cooling curves, driving force for solidification.
1.2 Casting Expendable mold casting(sand casting, plaster casting, shell casting investment casting), Non-expendable mold
casting, Evaporative pattern casting - lost-foam casting and full-mold casting.
1.3 Extrusion advantages of extrusion process, hot, cold and warm extrusion, micro-extrusion, extrusion defects
1.4 Drawing Processing of drawing, cold drawing and hot drawing, precautions and limitation
1.5 Forging Hot, warm and cold forging, advantages & disadvantages,
1.6 Rolling advantages and disadvantages of hot and cold rolling, terminologies, different types of rolling, assumptions of metal
rolling, defects in rolled products
1.7 Powder metallurgy process, importance and applications of powder metallurgy, advantages and disadvantages.
1.8 Fabrication through welding methods, glass and plastic welding fabrication, welding defects, Weld quality assurance, and
safety issues during fabrication through welding.
Materials processing
•Materials processing is defined as the series of steps or “unit operations”
used in the manufacture of raw-materials into finished goods. The
operations involve a succession of industrial processes with various
mechanical or chemical procedures, usually produced in large quantities or
batches.
• Industrial materials are defined as those used in the manufacture of
“hard”goods, such as more or less durable machines and equipment
produced for industry and consumers, as contrasted with disposable “soft”
goods, such as chemicals, foodstuffs, pharmaceuticals, and apparel.
✓ Lies above H-in ECS and ✓ Lies below H-in ECS and cannot displace
displace H2 gas from mineral acids. (dil. HCl H2 gas from mineral acids. (dil. HCl or
or dil. H2SO4) dil. H2SO4)
✓ eg: Li, Na, Mg, K, Fe, Zn , Pb etc.. ✓ eg: Cu, Hg, Ag, Au, Pt etc..
Mines Metal Ore Crushing and Pulverisation
Concentrated ore
Heat treatment
Calcination or Roasting
• Below the melting point, the energy of liquid becomes more than that of the
solid so below the melting point, the solid becomes more stable than liquid
• At melting point both liquid and solid have equal energy therefore both are
equally stable, hence no solidification or melting will occur at the melting point,
liquid will remain liquid and solid will remain solid at the melting point.
•Monomer attachment: Individual atoms or molecules are added to the surface of the nucleus one by
one. This is a common mechanism for crystal growth.
•Cluster attachment: Groups of atoms or molecules (clusters) can attach to the surface of the nucleus,
leading to faster growth. This is sometimes observed in the formation of nanoparticles.
•Oriented attachment: Two or more nuclei can merge together in a specific orientation, resulting in a
larger and more ordered structure. This is a common mechanism for the growth of biological tissues.
The interplay between nucleation and growth determines the final size, shape, and morphology of the new
phase. Understanding these mechanisms is crucial in various fields, such as materials science,
nanotechnology, and crystallography.
Nucleation and Crystals Growth
Solidification occurs by nucleation and crystals growth
• At the solidification temperature, atoms from the liquid like
molten metal, began to bond together and starts to form crystals.
• The moment a crystal begins to grow is known as nucleation and
the point is the nucleation point. Nucleation is the first step in
crystal growth. It's the process by which a small group of atoms or
molecules come together and arrange themselves in a specific
pattern. This pattern is the same as the pattern of the Multiple
crystals that will eventually begins to grow in the liquid phase.
• Final size of the individual crystals depends on the number of
nucleation point.
• The crystals increase in size by the progressive addition of atoms
and grow until they interrupt the adjacent crystal.
• Nucleation and crystal growth can happen in a variety of ways,
depending on the material and the conditions. For example,
crystals can grow from a solution, from a melt, or from a vapor.
a) nucleation of crystal b) crystal growth
They can also grow on a surface, such as the inside of a
container.
• The size, shape, and purity of crystals are all important
properties that can be affected by the way they grow. Nucleation
and crystal growth are therefore important processes in many
different fields, including materials science, chemistry, and
engineering. c) crystal growth d) grain boundaries
Ostwald ripening and Kirkendall growth principle
➢ fundamental mechanisms that explain the evolution of microstructures in materials, but they operate in different
ways and have distinct applications
➢ Driving force: Ostwald ripening is driven by differences in surface energy, while the Kirkendall effect is driven by
differences in diffusion rates.
➢ Outcome: Ostwald ripening leads to size changes within a single phase, while the Kirkendall effect leads to
changes in interface position and potentially new phases being formed.
Ostwald ripening: Kirkendall growth:
•Mechanism: Smaller particles dissolve faster than larger •Mechanism: When two materials with different diffusion rates
ones due to higher surface energy. Dissolved material are joined in contact, the faster diffusing species migrates into
diffuses and deposits onto bigger particles, leading to growth the slower diffusing material, creating voids at the interface. The
of the larger particles and shrinkage of the smaller ones. material on the slower side fills these voids, leading to an overall
•Applications: growth of the interface on the slower side.
Grain growth in materials: Controlling grain size in metals •Applications:
and ceramics influences properties like strength, ductility, and •Solid-state bonding: Joining dissimilar materials without
conductivity. Ostwald ripening can be used to achieve melting relies on the Kirkendall effect to create interdiffused
specific grain sizes. layers at the interface, ensuring strong bonds.
Production of monodisperse nanoparticles: Ostwald •Formation of metallic alloys: Diffusion of different metals at
ripening can help narrow down the size range, yielding more different rates leads to characteristic intermetallic phases with
uniform nanoparticle suspensions. desired properties.
Photovoltaic materials: Tailoring the size and distribution of •Microelectronic devices: Controlling the diffusion of dopants
pores in solar cell materials can enhance light absorption and in semiconductors is crucial for creating specific electrical
charge transport. characteristics. The Kirkendall effect plays a role in this process.
Grain types structure
❖ Grain types and structure play a crucial role in metal processing, significantly impacting the final properties and
performance of the metal product.
❖ Metals are not made up of uniform, amorphous blobs of atoms. Instead, they are comprised of tiny crystalline regions
called grains. Each grain is a single crystal, meaning its atoms are arranged in a repeating, ordered pattern.
❖ The boundaries between grains are called grain boundaries, where the crystallographic orientation of the neighboring
grains changes abruptly. These boundaries can significantly affect the mechanical and physical properties of the metal.
Polycrystalline – solidifies
the metal containing many
crystals
Grains-crystals in solidified
metal
Grain boundaries- the
surface between the grains
Factors Influencing Grain Structure:
The type and size of grains in a metal are influenced by various
The factors which determine
factors, including:
the rate of phase change are:
•Cooling rate: Faster cooling typically leads to smaller grains.
❖ The rate of nucleation i.e.
•Presence of impurities: Impurities can hinder grain
the no. of nuclei formed
growth, resulting in finer structures.
in unit volume
•Deformation processes: Cold working can break down grains
❖ The rate of growth i.e.
and refine the structure.
rate of increase in radius
•Heat treatment: Annealing can promote grain growth, while
with time
recrystallization can create new, smaller grains.
Shrinkage
Shrinkage - Most materials contract or shrink during solidification and cooling.
Shrinkage is the result of:
– Contraction of the liquid as it cools prior to its solidification
– Contraction during phase change from a liquid to solid
– Contraction of the solid as it continues to cool to ambient temperature.
• Shrinkage can sometimes cause cracking to occur in component as it solidifies.
• Since the coolest area of a volume of liquid is where it contacts a mold or die, solidification usually begins first at this
surface.
• As the crystals grow inward, the material continues to shrink.
• If the solid surface is too rigid and will not deform to accommodate the internal shrinkage, the stresses can become
high enough to exceed the tensile strength of the material and cause a crack to form.
• Shrinkage cavitation sometimes occurs because as a material solidifies inward, shrinkage occurred to such an extent
that there is not enough atoms present to fill the available space and a void is left
Shrinkage porosity
• This shrinkage defect is a characteristic for the central regions of castings (ingots) of the alloys with a wide
temperature range of solidification. In these castings “feeding” melt is not able to infiltrate through the
interlacing dendrites. The local micro-spaces between the dendrites arm remain isolated from the melt in riser
forming micro-cavities or shrinkage porosity.
• Gas pores, entrapped in the solid structure of a casting, arise from different origins. Generally the Gas (Hydrogen)
dissolved in the liquid during melting and when it cools down and solidifies hydrogen solubility decreases and it is
forced out from the melt. The gas bubbles are trapped by the dendrites, forming gas porosity.
Cooling curves
Pure metal solidifies at a constant If a pure metal cools rapidly and
temperature equal to its freezing does not contain any impurities as
point(melting point) nucleus to start solidifiction may cool
as in the fig.
Cooling curve for pure metals
❖ Casting and solidification are most
often used for making complex
shapes that would be difficult or
uneconomical to make by other
methods, and remain among the
most important commercial
processes for many materials.
❖ The modern science of
solidification started in the 1940s,
when engineers and scientists
began to use analytical
mathematical models to describe
solidification phenomena.
Solidification of Metals
Solidification
❖ Solidification, is a phase transition in which a liquid turns into a
solid when its temperature is lowered below its freezing point.
• Solidification is applied to a wide range of
materials from metals and alloys to ceramics and
polymers.
• Major practical application of solidification – Casting
Thermodynamically, both liquid and solid have equal energy at melting point
and therefore both are equally stable at melting point.
➢ Freezing (solidification) is almost always an exothermic process,
meaning that as liquid changes into solid, heat is released.
➢ This heat must be continually removed from the freezing liquid or the
freezing process will stop.
➢ The energy released upon freezing is a latent heat and is the entropy part.
➢ Some under-cooling will be essential for solidification.
➢ Solidification occurs by two process : nucleation and growth.
COOLING CURVES
❑ A cooling curve is a graphical plot of the changes in temperature with time for a material over the entire
temperature range through which it cools.
❑ Under equilibrium, all metals exhibits a definite melting and freezing points. If a cooling curve is plotted for pure
metal it will show horizontal line of melting and freezing temperature.
Freezing point
➢ In alloys solidification doesnot take place at
constant temperature
➢ Solidification occurs in a range of temperature so a
pattern will be formed
COOLING CURVE WITH UNDERCOOLING (Supercooling)
Undercooling or supercooling is the process of lowering the temperature of a liquid or a gas below its freezing
point without it changing into solid.
DRIVING FORCE FOR SOLIDIFICATION
Solidification is undoubtedly the most important processing route for
metals and alloys. As in fig.
Tf , ΔG = 0 so that
Where ΔHf is the latent heat of fusion and ΔSf is the positive for
melting
❖ the sand used is finer than sand casting sand and is mixed
with a resin so that it can be heated by the pattern and
hardened into a shell around the pattern.
➢ Investment casting derives its name from the fact that the pattern is invested, or surrounded,
with a refractory material.
➢ the wax patterns require extreme care for they are not strong enough to withstand forces
encountered during the mold making.
➢ generally used for small castings an expensive process compare to sand casting and die
casting.
➢ can incorporate intricate contours, excellent finish, so require little or no rework once cast
➢ this process has been used to produce aircraft door frames, blades for gas
turbines, in jewelry etc.
Non-expendable mold casting
Non-expendable mold casting differs from expendable processes in that the mold need
not be reformed after each production cycle. This technique includes
: permanent, die, centrifugal, and continuous casting.
❑ the most common process uses gravity to fill the mold. However, gas pressure or
a vacuum are also used.
❑ common casting metals are aluminium, magnesium and copper alloys. Other
materials include tin, zinc and lead alloys and iron and steel are also cast in graphite
molds.
The permanent molding process
Die casting
✓ metal is poured into the center of the mold at its axis of rotation.
Due to centrifugal force the liquid metal is thrown out towards the
periphery.
✓ Small art pieces such as jewelry are often cast by this method
Features of Centrifugal Casting
• Size limits are upto 3 m (10 feet) diameter and 15 m (50 feet)
length.
Lost-foam casting
Lost-foam casting is a type of evaporative-pattern casting process that is similar to investment casting except foam
is used for the pattern instead of wax. This process takes advantage of the low boiling point of foam to simplify the
investment casting process by removing the need to melt the wax out of the mold.
Full-mold casting
Full-mold casting is an evaporative-pattern casting process which is a combination of sand casting and lost - foam
casting. It uses an expanded polystyrene foam pattern which is then surrounded by sand, much like sand casting. The
metal is then poured directly into the mold, which vaporizes the foam upon contact