CSWIP 34U FEB 25 Part1
CSWIP 34U FEB 25 Part1
COURSE BRIEFING
START: 23 FEBRUARY 2025
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CSWIP 3.4U - Underwater Inspection
Controller
Contents
Section Subject
Preliminary pages
1 Engineering Offshore Structures
1.1 General background
1.2 Design specifications
1.3 Construction activity monitoring system
1.4 Guidance on design and construction
1.5 General design considerations
1.6 Pipelines
1.7 Offshore oil terminals
1.8 Future trends
2 Offshore Structures and Installations
2.1 Introduction
2.2 Steel production platforms
2.3 Terminology
2.4 Concrete and steel gravity platforms
2.5 Terminology associated with different offshore structures
2.6 Floating production storage and offloading units (FPSO)
2.7 Inspection of FPSO systems
3 Loading on Offshore Structures Engineering Concepts
3.1 General introduction
3.2 Properties of materials
3.3 Mechanisms of fracture
3.4 Stress concentration
3.5 Residual stresses
3.6 Forces on a structure
4 Deterioration of Offshore Steel Structures
4.1 General comments
4.2 Categories of deterioration and damage
4.3 Accidental damage
4.4 Corrosion
4.5 Fatigue
4.6 Wear
4.7 Embrittlement
4.8 Structural deterioration
4.9 Repairs to offshore structures
4.10 Repair inspection
15.1 Introduction
15.2 Advantages of video
15.3 Disadvantages of video
15.4 Videography systems
15.5 Video cameras
15.6 Video transmission standards
15.7 Video recording and storage
15.8 Ancillary video equipment
15.9 Deployment of underwater video
15.10 Preparation for deployment of underwater video
15.11 Practical techniques for underwater video inspection
15.12 Video commentary
15.13 Video pointer
15.14 Post-inspection
Course Objectives
To become competent to plan & co-ordinate a Subsea Inspection Programme
To become proficient in recording & processing data produced by Subsea Inspection Campaigns
To gain eligibility to sit the CSWIP 3.4U exam
Important note:
You must pass an end-of-course written examination to gain eligibility to take the CSWIP certification examination
This examination consists of:
Paper A – 50 multi-choice questions - 1hour 60% pass mark
Paper B – 10 written questions, one from a choice of two from 10 sections - 2 Hours 60% pass mark
You are allowed ONE re-test only should you fail this Exam (Test at the end of the course)
Practical Examination:
Data handling - 3 hours allowed for first part:
Data recording including data sheet & video log design
Your designed sheets will be photocopied & the originals handed back to you for your use
Report writing [300 - 500 words] - Audio commentary
Object description summary (approx. 150 words) - Telex/e-mail précis
Remainder consists of:
Work scheduling – 1hour 30mins
Isometric drawing evaluation – 1hour
Section 1
Engineering Offshore Structures
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1 Engineering Offshore Structures
1.1 General background
In the initial stages of development of offshore oil platforms, the designs evolved from
land-based structures and were constructed on site. During the 1950’s, Since then many
advances have been made, particularly in the field of materials. Governments’ legislation
has also played a role in shaping the design of production platforms.
Economics are very important and play a leading role in platform design. Not only
warrant the initial capital cost but will also guarantee a good income for a long period of
time. There is also a growing concern for the environment.
personnel qualifications.
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The Duty Holder is review of the current Safety Case at least every five years, or as
directed by the HSE. In addition, resubmit revisions that make a material change to the
HSE for acceptance (a material change such as significant modifications or repairs,
introduction of new activities, extension of life beyond original design life or major
changes in technology).
In addition to the Safety Case Regulations, the new goal-setting regulation (replacing the
previous prescriptive regulations) was introduced, as outlined below.
1.4.1 Guidance in UK regulations
The regulatory requirements for the asset integrity management of structures operated
on the UK specified in the following documents (Stacey, OMAE-49089):
The Offshore Installations (Safety Case) Regulations 2005 (SCR05), which make
preparation of a Safety Case a formal requirement (described above).
The Offshore Installations And Wells (Design And Construction, etc.) regulations 1996
(DCR), which require the Duty Holder to ensure that suitable arrangements are in place
for maintaining the integrity of the installation, through periodic assessments and
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The Pipelines Safety Regulations 1996 (PSR), which require the operator to ensure that
a pipeline has been designed adequately (it can withstand internal and external forces
arising from its operation); all hazards relating to the pipeline with the potential to cause
a major accident have been identified and the risks arising from those hazards have been
evaluated and that the Safety Management System is adequate.
The Provision And Use Of Work Equipment Regulations 1998 (PUWER), requires
employers to ensure that work equipment is fit for the purpose for which it is used;
Employers are required to identify and control potential risks from hazards due to
equipment failure; put in place appropriate inspection procedures after installation; and
appropriate inspection and maintenance procedure during service to ensure that the
work equipment is in efficient working order and in good repair.
ISO standards for offshore structures
Standards the ISO 19900 series giving guidance on the design, construction,
transportation, installation, integrity management and reassessment of offshore
installations.
Structures covered by these standards include: fixed steel structures; fixed concrete
structures; floating structures, such as FPSOs, semi-submersibles and spar platforms,
arctic structures and site-specific assessment of jack-up platforms.
The following ISO offshore structures standards have been published:
ISO 19900: 2002 General requirements.
ISO 19901 Specific requirements.
ISO 19901-1: 2005 Metocean design and operating considerations.
ISO 19901-2: 2004 Seismic design procedures and criteria.
ISO 19901-3: 2010 Topsides structures.
ISO 19901-4: 2003 Geotechnical and foundation design considerations.
ISO 19901-5: 2003 Weight control during engineering and construction.
ISO 19901-6: 2009 Marine operations.
ISO 19901-7: 2005 Station keeping systems for floating offshore structures and mobile
offshore units.
ISO 19902: 2007 Fixed steel offshore structures.
ISO 19903: 2006 Fixed concrete offshore structures.
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environments.
Mobile drilling units are jack-up or semi-submersible rigs, depending on water depth.
They can be used to drill production wells where size and economics of the reservoir do
not justify the installation of a platform.
1.8.2 Design practices
Fixed platforms are now lighter, slimmer and simpler than the giant platforms built in the
1970s.
General Background
Initially, design for offshore platforms taken from:
Civil engineering - Naval architecture.
The 1950’s saw new technology & many advances.
Structural design is also influenced by:
Government Legislation – Economics – Environment - Safety of Personnel.
Designers try to achieve a structure:
Elegant if possible - Conservative in material - Fit for purpose - Can operate for the design life - Safe to operate.
Within budget.
Quality Assurance (QA) function can be implemented. This can take the form of an Activity Monitoring
System:
Full certification by way of ‘As-built’ drawings.
Full material certification.
NDT - Inspection Certification – Personnel Qualifications.
With these engineering requirements in mind, design & structural engineers will be able to:
Obtain guidance as to what minimum standards are acceptable to the appropriate authority.
In 1988, a gas leak on the Piper (A) destroyed the platform & cost 167 lives.
A Public Enquiry, chaired by Lord Cullen, then made 106 recommendations aimed at improving safety.
The HSE developed “The Offshore Installations (Safety Case) Regulations” in 1992.
These require the Duty Holder to prepare Safety Cases for each installation in UK waters.
The HSE must accept these before operations are permitted.
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The Duty Holder has the ability to control major accident risks effectively.
This requires that the Duty Holder has identified the major hazards.
Implemented control measures to ensure that the risks are reduced to being: ‘as low as reasonably practicable’ (ALARP).
To be in compliance with all Statutory Provisions.
Make adequate arrangements for auditing & reporting.
The Duty Holder is to conduct a review of a Safety Case at least every 5 years or, as directed by the HSE.
Revisions that make a material change, are required to be re-submitted to the HSE.
A material change is one that changes the basis on which the original Safety Case was accepted:
Significant modifications or repairs.
Introduction of new activities.
Extension of design life. Major changes in technology.
Limit States.
ULS (Ultimate) Carrying loads.
FLS (Fatigue) Cyclic loading/unloading.
ALS (Accidental) Accident/failure.
SLS (Serviceability) Normal use or durability.
Offshore Pipelines are fabricated from high grade steel pipe (API-5LX).
Bitumen wrapped for corrosion prevention.
Coated with a layer of Gunite.
Sizes vary from 50mm to 914mm.
Wall thickness depends on pressure rating.
Temporary Topsides:
This design innovation allows for the removal of the derrick after drilling is completed.
Future Design Practices:
Continue to make structures slimmer & simpler.
The main emphasis to be the topside modules.
Greater use of sub-sea satellite technology.
These trends will help to reduce costs.
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Section 2
Offshore Structures and Installations
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2 Offshore Structures and Installations
2.1 Introduction
Some of the biggest installations are in the North Sea and consist of concrete gravity
structures.
Then there are the more common steel platforms, which can be of the eightlegged type
or may be of a lightweight four-legged variety. There are also jack-up rigs, which are
mobile, and tension leg platforms (TLP), which float.
Apart from these production facilities, there are also seabed wells, manifold centres and
thousands of kilometres of pipelines. Another common structure seen worldwide is the
single point mooring (SPM) which comes in a variety of designs, some of which
incorporate storage facilities.
2.2 Steel production platforms
With steel fixed platforms the jacket supports the superstructure, which contains all the
necessary facilities.
These types of platforms are sometimes referred to as steel piled structures because the
jacket is piled into the seabed. Once it is in the upright position, with piles either driven
through the legs or positioned around the main legs and driven through pile sleeves, so-
called skirt piles.
One example of the large fixed production platform is the Brent A, which is installed in
Shell-Expro’s Brent Field in the North Sea (figure 2.1).
An example of a lightweight platform servicing seabed wellheads and facilities is the
Gannet ‘A’ platform in Shell-Expro’s Gannet field in the central North Sea (Figure 2.2).
The structure is of the same basic design but not as massive as the production platform.
2.3 Terminology
The production platforms are the most massive installations and they may be of steel or
concrete construction, steel being the most prevalent. Both types have standard
components and a thorough working knowledge of this terminology is necessary to be
able to communicate with other engineers.
Figure 2.3 A steel platform.
Following is the common terminology for the components making up the steel sub-sea
structure:
Can: The vertical section making up a node, ie the main body of the node.
Conductor guide frame: Horizontal sections of framework, which restrain and guide
the conductors.
Leg or chord: Main vertical component, constructed from a number of sections welded
together, supporting the rest of the structure.
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Member: The horizontal, vertical diagonal or horizontal diagonal braces of the jacket.
Node: Point on the welded steel structure where two or more members meet and are
joined.
Pile guides: A steel cylinder that supports the pile while it is driven into the sea-bed.
Pile guides are mounted in clusters around each leg at various levels. They are usually
removed on completion of piling operations.
Pile sleeves: Long steel cylinders, grouped around the base of the legs into which the
piles are located before being driven into the sea-bed. The tops of the piles should be
level with the tops of the sleeves on completion of piling.
of disadvantages.
Stability problems during tow-out to site have to be counteracted by limiting the topside
weight, thus reducing the apparent advantage of large deck space fitted out in sheltered
waters.
The very heavy-lift derrick barges now available, thus reducing the cost of offshore steel
structure installations, and therefore, limiting the cost advantage of concrete
constructions.
Concretecannot withstand tensile forces, so the use of the base storage cells must be
carefully monitored at all times to avoid the storage of crude oil causing a build-up of
differential loadings between cells, thus causing excessive tensile stresses.
Also, pressure must not be allowed to build up in the cells; vapour pressure must not
exceed 2bar (30psi). Oil temperature in the cells must not exceed 38°C to avoid thermal
stresses. If crude oil is not carefully monitored, emulsions formed by the interaction of oil
and associated water can accumulate permanently within the cells.
Reservoir sand must not be allowed to accumulate and steps have to be taken to
eliminate this from the crude before it reaches the cells.
At least one of the main shafts will house utilities, and because it is some 100m tall and
very narrow, ventilating it is difficult, so breathing apparatus is issued to maintenance
staff working there, making routine maintenance and operations of the equipment
difficult.
Stagnant water accumulated in the structure encourages the growth of anaerobic
bacteria, which generate ideal conditions for the formation of sulphate reducing bacteria
(SRB).
The growth of SRB’s leads to the production of Hydrogen Sulphide (H2S), which
necessitates the creation of safety zones and special procedures to avoid risk to
personnel.
2.4.2 Basic components of a concrete gravity structure
Gravity structures may be made of steel or a mixture of steel and concrete, but the most
common is concrete. They are anchored to the seabed by their own mass, hence the
term gravity. Common features of this type of design are the large diameter columns
supporting the deck module and numerous ballast/storage cells making up the base.
Anchorage points (cachetage points)
Are an essential part of the tensioning components in pre and post-stressed concrete
structures. The anchorage point is cast into the concrete at the ends of the tensioning
tendon or bundle of tendons. It grips the tendon and thereby transfers the load from it to
the structural concrete. It is commonly encased in protective concrete domes
Breakwater walls
Are concrete walls in the splash zone, containing
cast in holes that dissipate the wave energy and
thus protect the structure within the walled area.
Tetra pods
Are four-legged concrete blocks that are used on
jetties and sea shores to break up the wave-slam.
Jarlan holes
Term used to describe the cast in holes in the
breakwater walls, used to break up waves to
reduce their force on the structure ahead.
Support columns
The concrete or steel columns supporting the deck module.
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Support domes
The tops of the tanks, at the base of the structure, which are used as buoyancy during
the launch of the structure, may then be used to store oil, water or drilling mud.
connected to seabed wells by flexible risers (Figures 2.19 and 2.20). Vessels may be
purpose built, or converted and may be mono-hulls or semisubmersible.
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Tankers, for example can be converted for this task relatively quickly and cheaply.
In this case they are usually known as Floating Production Storage and Offloading Units
(FPSO). These vessels are quite weather dependent, which is why purpose built vessels,
have been developed.
2.6 Floating production storage and offloading units (FPSO)
FPSO’s have been used since 1977 when the first was installed off Spain. A schematic of
an FPSO setup is shown in Figure 2.21.
Currently there are more than 650 sub-sea wells. These structures can offer advantages
over platforms to:
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2.7.2 Pipelines
Are used extensively for the transport of crude oil and gas. Traditional pipelines are
constructed of steel and may be made up of nominal 40 foot (12.0m) lengths of pipe
sections up to 3 feet (0.9m) in diameter which are
welded together. Grade of steel used AP1 5LX.
Alternatively, smaller diameter steel pipe up to 2
foot (0.6m) diameter can be laid up onto special
reels and then laid in long lengths off the back of
specially designed reel-laying vessels.
Modern developments in materials have led to the
widespread use of composite pipes made of a
variety of polymers. One such pipe is known as
Coflexip. This type of pipe is commonly laid from
specially designed reels off the back of suitable
vessels.
Figure 2.28 Gullfaks flowline bundle.
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Section 3
Loading on Offshore Structures
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3 Loading on Offshore Structures
3.1 General introduction
The strength a material needs to have and how thick it needs to be, stress, defined by
the load a material can support by area of the cross-section taking the load, is used.
Stress is used so that comparisons with loading on other structures, of different sizes and
shapes, can be made.
Stress is defined as the force (or load) divided by the cross-sectional area carrying that
load. Stress is denoted by the Greek letter (sigma) and is defined mathematically as:
or stress = Load or force = F/A
Area
Types of stress
Tensile stress: Load trying to pull a component apart,
Compressive stress: The opposite of tensile stress, in compression, a component or
structure is being pressed together
Bending: Structures are sometimes loaded so that they are subjected to a mixture of
tensile and compressive stresses. A simple beam supported at the ends and loaded in
the middle is a good example.
Adhesive
When two surfaces rub together it causes
friction and to explain this it is assumed that
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Abrasive wear
In the mechanism for abrasive wear, a hard particle in one surface indents, grooves
and then cuts material from the other surface. In service, the main cause of abrasion
between sliding metals is the presence on one of the two surfaces of particles of hard
materials, such as carbide in steels, work hardened wear fragments or hard oxide films.
The particles may also be air or waterborne dirt such as grit.
Wear caused by fatigue
When there is relative motion between two surfaces in contact, the state of stress at
any given point on or near the surfaces varies with time and this may cause fatigue, the
slow growth of cracks. The development of such cracks may eventually detach pieces of
material from the surfaces, thereby constituting wear.
Chemical and corrosive wear
Chemical effects are most commonly exemplified by the repeating cycle of the
formation, removal and reformation of oxides (Rust films).
4.7 Embrittlement
In service could come about due to incorrect welding procedures or by the absorption of
a gas, generally hydrogen. It has been encountered in natural gas pipelines and could
also come about from the absorption of hydrogen produced by an overprotective
impressed current corrosion protection system or associated with sour service. The
temperature of the environment affects the brittle behaviour of steel, brittle fracture
being more likely to occur at low temperatures.
4.8 Structural deterioration
Types of failures for offshore steel structures are divided the life of a structure into four
stages. At every stage defects leading to deterioration and then failure can occur.
4.8.1 Stage one – production of the raw materials
During the manufacturing of the raw
materials, several defects can be
included into what will become the
parent plate, pipe or profile. Defects
include laminations, pores, segregation
of undesirable inclusions, incorrect
chemical composition or heat treatment
condition.
laminations.
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the end result of a defect initiated at the fabrication stage. Fatigue is the major cause of
component failure in-service.
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This type of failure may be avoided if the crack is identified at an early stage, before it
propagates. It can be considered to be a notch at this stage and profile grinding will
remove this defect. This will reduce the weld throat thickness and the wall thickness,
however, provided this is kept within design parameters and a smooth profile is
achieved, the possibility of failure is more remote.
Corrosion
An important form of structural deterioration, which is covered in detail in sections 7-10.
Physical damage
This form of deterioration is generally caused by either collision or impact damage
caused by components being dropped. All accidental damageshould be reported
immediately so that it can be assessed.
The foundations of a structure are an obvious area susceptible to movement of material
on the seabed. Any movement is likely to weaken the foundations which, of course,
jeopardises the whole structure.
4.8.6 In-service defect categories that affect both steel and concrete
The in-service defects listed for steel can also affect concrete. Concrete structures may
suffer from cracks, the reinforcement may corrode and physical damage and scour is
also quite possible. Cracks in the concrete surface are less serious than cracks in steel
because offshore structures fall into the pre-stressed category and major components
are therefore kept in compression.
There are other considerations that do affect both steel and concrete structures and that
may cause defects in service:
Inter-tidal and splash zones
The inter-tidal and splash zones on any structure are regions of particular susceptibility
to deterioration:
Corrosion is more aggressive in this area and must be more carefully monitored.
Marine growth build-up is greater in the top 20m of the sea and is particularly dense in
the inter-tidal region. This will increase mass and drag in a part of the structure most
vulnerable to these effects. Marine growth may also affect corrosion rates.
The risk of physical damage is greater in this region due to the risk from floating
objects.
Risers
Are components common to both types of structures, although on concrete platforms
they may be installed inside the shaft. Risers are inspected annually because they can
suffer the same deterioration as pipelines. The clamps, guides and flanges are subjected
to the same regime.
Conductors and conductor guide frames
They are exposed to the same risk of failure as risers, perhaps more so as there are
greater vibrations possible with these components than the rest of the platform.
Furthermore, conductors are normally kept in place by guides rather than clamps, which
allow relative movement between the conductor and its guides; hence wear must be
monitored, as there is a real possibility for fatigue cracking to occur.
Caissons
The pump at about 18m water depth is commonly suspended from the surface inside the
caisson. Conditions at this point on the inside of the caisson are near perfect for
corrosion to progress at excessive rates. This has caused component failure on more
than one occasion.
Overloading
Changes in the working practices and other commercial factors may lead to extra items
of equipment being installed, such as a newer, bigger crane and needs carefully
monitored.
4.9 Repairs to offshore structures
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The Duty Holder’s engineering department will make a decision on what course of action
to take depending on the severity of the defect and its position on the structure. The
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and by evaporation from the surface. It is true to say that the less excess water in the
concrete mixture; the stronger the final material. Thus, it is beneficial in terms of
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material strength to limit the water to the minimum possible whilst still maintaining the
required workability.
If the water content is too high then proliferation of capillary voids will result in a porous
and weak material. Also, as the excess water migrates to the surface to be lost by
bleeding and evaporation, then volume shrinkage will occur in the outer layers of the
concrete. This shrinkage effectively tightens the surface of the concrete over the sub-
surface layers forming a skin of tensile stress. As concrete is relatively weak in tension
this often leads to plastic shrinkage cracking.
If there is embedded steelwork like reinforcement close to the surface of the concrete,
then excessive water may also lead to settlement of aggregate particles around the
steel. This may result in plastic settlement cracking which will mimic the pattern of
the reinforcement.
Hydration is an exothermic reaction – that is, it generates heat. If a large amount of
concrete is poured all at once then the heat produced during the hydration process
causes the sub-surface material to expand. Cooling at the surface causes contraction
and a skin of tensile stress forms. This may cause thermal cracking. Thermal cracking
may be avoided by limiting the bulk of each pour or by laying sacrificial chilled-water
pipes within the mould.
As the concrete hydrates it moves from a liquid state, gradually becoming increasingly
viscous until it sets as a solid. During this time the alkalinity stabilises at around pH
12.5.
After the concrete has set to a solid a period of curing continues during which silicon
polymers form. The initial cure phase is considered to last from a number of days to a
number of weeks, during which time the temperature and evaporation must be carefully
controlled.
In fact, concrete reaches around 70% of its final strength after the initial cure and around
90% of its final strength after about one month. After that the material very slowly
becomes harder and stronger, reaching full maturity after around 27 years.
To control temperature and evaporation during the post-placement cure, the concrete is
often protected from the environment by covering with fabric or plastic sheeting or using
spray system to reduce the likelihood of cracking.
Concrete slabs may be flooded with water during this time for the same reason (called
ponding). Vertical walls such as slip-formed structures may be painted with curing
compounds and curing compounds may be removed or left in place following the initial
cure.
5.4 Additives
Additives (termed admixtures) are chemicals that are added to the concrete mix to
enhance its properties or to change its workability or rate of hydration:
Plasticizers: By adding a plasticizer we may reduce the water content of the mix yet
still retain adequate workability during construction. For this reason, plasticizer is
sometimes referred to as water-reducer.
Accelerators/retarders: These chemicals change the rate of hydration to suit the
construction method used. It is sometimes critical to accurately control the rate at which
the concrete sets, eg when slip-forming.
Others: The final properties of the concrete may be enhanced by the addition of other
admixtures. For example, a water-retardant may be added to enhance resistance to
penetrating water.
5.5 Loading on concrete
Concrete is extremely strong when loaded in compression. It also has very good
compression stiffness. Unfortunately, it is relatively weak when loaded in tension or
shear.
Engineers may design a structure or a component to avoid loading the concrete in
tension or shear. For example, a concrete dam.
However, tension and shear cannot always be avoided by design. For example, when a
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beam is supported at either end and is loaded from above, we see that the lower face will
be in tension and that shear stress is imposed at either end.
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In this case, the concrete can be strengthened by embedding reinforcement or by using
a pre-stressed beam.
5.6 Types of concrete
There are several types of concrete that are commonly used in construction:
5.6.1 Grout
Grout is a mixture of cement and water. It may contain admixtures but does not contain
any aggregate.
It is obvious when we consider that the strength of concrete comes from its aggregate
that grout is not a strong material. It is, however, flexible and so is used where we
require some movement in the structure.
Typical applications for grout include:
Sealant, to seal construction joints.
Filler or packing material, between steel piles and the pile-sleeves.
Repair material, typically for relatively small areas of repair.
Grout is never used as a structural material.
5.6.2 Mortar
Mortar is a mixture of fine aggregate (sand), cement and water. It often also contains
admixtures.
Since mortar contains fine aggregate, it is stronger than grout but is still significantly
weaker than concrete. Like grout, it is used when some flexibility is required. It is often
used as a jointing material – effectively forming a flexible interface between two stiffer,
stronger components.
Typical applications for mortar include:
Jointing - Sealant - Filler or packing material - Repair material.
The same as for grout, mortar is not used as a structural material.
the high pH (around 12.5) of the material. This stimulates the formation of a passive
skin of Fe2O3 oxide around any embedded steelwork. As a result, the steel is passivated.
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It is very important that the passive environment around the reinforcement is maintained
and that no water is allowed to seep in around the steel.
The current standard relevant to concrete structures is EN 1992: Design of Concrete
Structures, (Eurocode 2). This standard replaces CP110 under which many existing
structures were built. Both standards require a minimum cover of 60mm over any
embedded steel reinforcement (between the steelwork and the outside environment) in
order to protect against water ingress causing loss of passivation.
If passivation is lost by water ingress causing chloride attack or by carbonation, then the
Fe2O3 oxide skin will be lost and replaced by Fe2+. This form of oxide expands as it forms,
creating an increase in volume of the oxide layer around the re-bar. This effectively
pushes the concrete apart in the area local to the corroding reinforcement.
A shear zone is created around the expanding oxide and the concrete will eventually fail
in shear. This failure is characterised by a crack along a 45° line to the action of the
shear stress. The resulting defect is therefore characterized by a 45° crack surrounding
material that has been pushed away from the surface of the concrete.
Depending upon the orientation of the
re-bar relative to the surface of the
concrete, this process will result in a
popout or delamination – see Figure
5.3.
A popout as the end of the re-bar pushes a cone of concrete away from the surface. A
delamination where a plate of material comes away from the surface. Both are forms
of spalling – a general term used to describe the loss of material from the surface of
concrete.
5.10.2 Columns
Columns of concrete structures may be dry or free-flooding. Indeed, there may be both
types on the same structure with one column acting as a utility shaft containing risers
and conductors. In such shafts, bacterial attack may lead to the release of hydrogen
sulphide gas and great care must be taken to ensure that the column is sufficiently
ventilated.
5.10.3 Expansion joints
Expansion joints are narrow gaps, which are sometimes left between large masses of
concrete to allow for thermal movement. Even if in-service thermal variations are not
significant, expansion joints may be required to allow for movement during the hydration
phase of the construction.
On offshore structures, expansion joints may allow for thermal movement caused by
storage of hot production fluids or to allow some structural flexibility.
Often, expansion joints will be sealed with a flexible sealant such as bitumen
5.10.4 Tow-out, placement and commissioning of concrete structures
Once completed, the structure is towed to location by tugs. When positioned correctly, it
is ballasted to sink gently to the seabed. The structure is maintained in an upright
orientation during this phase, limiting the imposed bending moments. Depending on the
nature of the substrate and underlying rock, the structure may sit directly on the bed of
the sea or on a prepared foundation (Base raft).
Once on the seabed, on-bottom mass is increased by further water ballasting and
possibly also solid ballasting using dense material such as iron ore. Suction anchors or
skirt piles may also be employed to aid stability.
It should be noted that not all of the cells in the caisson of the structure will be used for
ballast – cells are also available for storage of production fluids and product.
Loading of the deck, modules and superstructure may take place at the construction site
or at the final location utilising heavy-lift barges.
5.11 In-service deterioration of concrete structures
Concrete structures deteriorate by two means – physical and chemical attack:
5.11.1 Physical attack
Physical attacks include the following assaults:
Impact – the inter-tidal zone is most at risk of impact damage from floating objects.
Overload – eg storage cells need careful management to avoid overloading diaphragm
walls with hydrostatic imbalance.
Freeze/thaw cycles التجمد والذوبانcan attack the exposed part of the structure forcing
small crevices الشقوقand cracks to widen and eventually lead to spalling. تقشير
Expansion of reinforcement caused by corrosion can lead to cracking and spalling.
Abrasion – concrete is relatively easily abraded التاكلand care must be taken to avoid
any rubbing or fretting of concrete surfaces.
During the alkali-silica reaction, silica forms a gel and begins to absorb water.
The gel swells and starts to exert an internal pressure within the concrete. Gel may
weep )يسيل (يتسربfrom the surface of the concrete (exudation) and can lead to
expansion, cracking and spalling.
5.11.4 Sulphate attack
Seawater contains sulphates that, if allowed to penetrate into the concrete, will react
with the hydrated cement to form a crystalline solid called ettringite (calcium-
aluminium sulphate). This causes a volume expansion, leading to cracking and spalling.
5.11.5 Chloride attack
If seawater seeps next to the steel reinforcement within the concrete then chlorides will
destroy the passive iron (3) oxide skin. This will initialise the reinforcement corrosion
process– Reinforced concrete, eventually resulting in cracking and spalling.
5.11.6 Carbonation
If atmospheric carbon dioxide reaches the steel reinforcement within the concrete then
passivation will be lost in a similar way to chloride attack. This will eventually result in
reinforcement corrosion, cracking and spalling.
Although carbonation is a theoretical risk for an offshore structure, if it has been built
according to either EN 1992 or CP110, then the process would be too slow to pose any
real threat to an offshore structure, although a crack could theoretically speed up the
process.
5.11.7 Biological attack
Under anaerobic conditions, sulphate-reducing bacteria living in the small voids in the
concrete produce hydrogen sulphide. Some of this gas may escape to the surface of the
material and if allowed to build up, can pose تشكلa significant health risk.
However, some of the hydrogen sulphate may be captured by aerobic bacteria that
oxidise it to form sulphuric acid. This will dissolve away the carbonates from the
hydrated cement and weaken the material. Eventually this will lead to cracking and
spalling.
5.11.8 Corrosion of inset steelwork
If, for example, the anchor point for an external fixing such as a riser clamp should make
electrical contact with the embedded reinforcement, then a corrosion cell will form. In
this case, the embedded part of the inset steelwork becomes cathodic and the external
part of the steelwork becomes anodic, leading to accelerated corrosion.
5.12 Imperfections of concrete
The U.K. government has published an offshore technology report (OTH-84-206)
that categorises twenty six imperfections that may be seen on concrete structures. This
report defines three categories:
1 Category A: Defects. 2 Category B: Areas of Concern.
3 Category C: Blemishes.
These imperfections may be either a construction or an in-service imperfection
5.12.1 Category A: Defects
Category A (defects) usually require detailed investigation and are likely to generate an
intervention to repair the defect.
The category A (defects) are:
Cracks - Impact damage - Popouts – Delamination - Variable cover – Exposed –
reinforcement - Tearing - Poor repairs.
Popouts and delamination may be referred by the general term of spalling – the loss of
material from the surface of the concrete.
5.12.2 Cracks
Cracks may form because of:
Plastic shrinkage cracking.
Plastic settlement cracking.
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Thermal cracking.
Overload.
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Freeze/thaw cycles.
Alkali-aggregate reaction.
Settlement cracking.
Internal corrosion.
Sulphate attack.
Cracks may take the form of individual, distinct general cracks, or of a network more
fine pattern cracking – see Figure 5.18.
5.12.3 Category B: Areas of concern
These will usually be monitored but may require an intervention to repair.
The category B (areas of concern) are:
Embedded objects. Embedded objects (wood and wire-ties).
Recessed metal plates.
Cast-in sockets. Soft edges indicate that this is a cast-in socket
and not one that was drilled after the concrete had set.
Abrasion.
Water-jet damage.
Honeycombing. is caused by lack of consolidation during
placement
Due to the problems in navigating and location reporting when inspecting concrete
structures, very often ROVs are used in preference to divers.
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Invert
The lowest point of an opening or tunnel.
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Soffit
The underside of a concrete beam.
Jarlan hole
Perforation in a breakwater wall, used to dissipate the forces from wave action, some of
the force will be repelled and some will be admitted through the wall where the Venturi
principle dissipates the energy thus reducing the forces acting on the wall.
Laitance
This is a fine powdery substance, which accumulates on the surface of concrete as it
sets; it will need to be removed prior to any new pour being applied.
Exudation
Exudation consists of salts, which dissolve, in the concrete when fluid is passing through
a crack; it shows on the surface of the concrete as a whitish semi-fluid, which
accumulates around the crack.
Note: On the surface it will always run downwards, however in water it may drift
sideways or even upwards, owing to the fact that its density may be less than the water
around it.
Aggregate is a hard material that is responsible for the compression strength & stiffness of concrete.
Aggregates may be:
Quarried from land sites.
Manufactured by crushing larger rocks.
Harvested from beaches.
If from a beach, it may contain significant levels of salt, & must be washed thoroughly in fresh water
After concrete has set, a period of Curing continues, during which, silicon polymers form.
The initial cure may last from days to weeks.
Temperature & evaporation must be controlled.
70% of its final strength after the initial cure.
90% of its final strength after one month.
Full maturity after around 27 years.
Admixtures - chemicals added to the mix to enhance its properties, change its workability or hydration rate.
Plasticizers - added to reduce the water content.
Accelerators/Retarders - used to change the rate of hydration to suit the construction method.
Water-retardant - added to enhance resistance to penetrating water.
Concrete is strong when loaded in Compression.
Relatively weak when loaded in Tension or Shear.
Engineers design a structure to avoid loading it in tension or shear.
A concrete dam is often curved in order to translate the hydrostatic pressure on the convex side of the dam, into
compressive stress within the dam wall.
Grout is a mixture of cement & water.
It’s not a strong material, but it is flexible.
Used where some movement is required.
Typical applications include:
To seal construction joints.
Packing between piles & pile-sleeves.
Repair material, for relatively small areas.
Grout is never used as a structural material.
Plain Concrete is a mixture of sand, gravel, cement, water & often, admixtures.
The term ‘Plain Concrete’ refers to the fact that it does not contain any reinforcement.
Typical applications include:
Structural elements that are loaded in compression.
Repair material, typically for relatively large areas.
Reinforced Concrete.
Plain concrete with embedded steelwork.
The function of the steel is to take any tensile or shear loading.
Reinforcement is only laid in locations which will be subject to tension &/or shear.
Reinforcement-bar or Re-bar is, usually, round-section, ribbed bar with a diameter of between 10mm & 50mm
When first loaded, a reinforced component will deform as it takes the strain.
The concrete may crack as the re-bars take up any tensile or shear stresses.
This is common & is known as Settlement Cracking.
Re-bar is protected from corrosion due to the high pH.
This stimulates the formation of a passive skin of Fe2O3.
The passivation must be maintained & no water is allowed to seep in.
EN 1992 Design of Concrete Structures (Eurocode 2).
Replaces CP110 under which, many existing structures were built.
Both Standards require a minimum cover of 60mm over any steel reinforcement
If passivation is lost by water ingress causing Chloride attack, or by Carbonation, then the
Fe2O3 skin will be lost & replaced by Fe2+. This form of Ferrous Oxide expands as it forms, creating an increase in
volume of the oxide layer around the re-bar.
This pushes the concrete apart in the local area.
A Shear zone is created around the expanding oxide & the concrete will eventually fail in shear.
Depending upon the orientation of the re-bar, this process will result in either: Popout or a Delamination.
Both are forms of Spalling – a general term used to describe the loss of material from the surface.
Pre-stressed concrete contains steel rods or tendons that run within the component.
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Pulled to a predetermined tension & locked into anchor points (Cachetage Points).
The tension is calculated to be greater than any in-service tensile stress, so the concrete is kept in compression.
Pre-tensioned tendons are stressed before the concrete is placed.
Post-tensioned components are built with conduits within them.
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The tendon is placed within the conduit & stressed, using screwthreads or a stressing ram, after the concrete is placed.
Once the tendons are locked into the cachetage points, grout is injected into the conduit to protect the steel by
passivation.
As the concrete is maintained in a compressive load, this type should not exhibit any settlement or in-service cracking.
type of concrete covering of a pipeline, actually a form of mortar called Gunite.
Primary function is to control the buoyancy, to ensure sufficient on-bottom mass to maintain stability.
It has the secondary functions of:
Impact protection.
Corrosion protection.
Organic Polymers are often found associated with concrete structures, e.g. Epoxy.
Typical applications include:
As a sealant.
As repair material for relatively small areas.
As bonding material.
Injected into the surface of concrete to stabilise it.
Readily identified by their hard, glassy texture.
Before concrete can be placed, it must be produced, usually in bulk, in a concrete plant.
Such plant may be sited at the construction yard.
Structure is built in the upright orientation, from the ground upwards.
Smaller structures may be entirely constructed in the yard then towed out when completed.
With larger structures, once they reach a certain height the yard is flooded & the structure moved to sheltered water for completion
There are three basic methods used to place the concrete:
Pre-casting.
Fixed-shuttering.
Slip-form shuttering.
Pre-cast concrete is manufactured in a factory & used to produce multiple items of a certain design - pipe sections.
High-quality, re-usable moulds are used, which give a good surface finish.
With fixed-shuttering construction, walls, called Formwork, are built to contain the concrete while it sets.
Height is limited by the hydrostatic pressure exerted on the bottom of the formwork by the wet concrete.
When the concrete is placed within the formwork, it is consolidated by vibration or tamping.
When the concrete has set, formwork may be removed & reassembled higher up, ready for the next pour.
Formwork systems available:
Wooden formwork.
Versatile & useful for creating complex shapes.
Engineered formwork. Re-usable
steel/aluminium.
Plastic formwork.
Re-usable plastic modules.
Structural formwork.
Not removed after the
concrete has set – forms part of the reinforcing system.
Fixed-shuttering requires that each successive layer of
concrete sets sufficiently to allow for removal/reassembly of the formwork:
This causes a series of horizontal Construction Joints.
These are weak points in the structure in terms of lateralshear & are potential places where water may penetrate.
To seal the joint, it is often rebated then filled with sealant, such as grout, mortar, bitumen or epoxy.
when constructing tall components with unchanging shape, such as columns.
The formwork is built onto a jacking system.
Concrete is continually placed within the slip-form & as it fills with material, it is jacked upwards using hydraulic rams.
The typical rate of climb is 200 to 250mm per hour.
Slip-form is continually moving as the concrete is being placed.
There’s no construction joints.
As the slip-form moves upwards, the concrete exposed at the lower skirt tends to bulge slightly.
Gives rise to a characteristic feature of slip-form – regular horizontal ridges known as Weatherboarding.
Other features characteristic of slip-formed structures:
Irregular horizontal ridges caused by slight variations in the concrete & the construction process.
Vertical drag marks caused by minor debris being trapped between the formwork & the structure.
Without the Slip-forming method, offshore structures would simply take too long to build.
Jarlan Holes.
Sometimes found set into concrete breakwater walls & anti-scour fences.
At a critical velocity, the flow becomes turbulent & so dissipates the fluid energy, reducing the hydrodynamic loading.
Columns of concrete structures may be dry or free-flooding.
There may be both types on the same structure, with one acting as a utility shaft, containing risers & conductors.
In these, bacterial attack may lead to the release of H2S.
Great care taken to ensure that the column is ventilated.
Expansion Joints - narrow gaps, sometimes left between large masses of concrete to allow for thermal movement.
May be required to allow for movement during hydration.
Allow for thermal movement caused by storage of hot production fluids or to allow some structural flexibility.
They will be sealed with flexible sealant such as bitumen. structure is towed to location by tugs.
On location, it’s ballasted to sink to the seabed.
Depending on the nature of the substrate, the structure may sit directly on the seabed or on a Base Raft
Once on the seabed, mass is increased by water or iron ore.
Not all the cells will be used for ballast, some are available for storage of production fluids.
Loading the superstructure may take place at the construction site or at the final location using heavylift barges.
Concrete Structures deteriorate by two means:
Physical attack & Chemical attack:
Physical Attacks include:
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Impact Damage.
Overloading.
Freeze/Thaw Cycles.
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Corrosion of Reinforcement.
Abrasion.
Chemical Attacks include:
Alkali-aggregate Reaction (AAR).
Sulphate Attack.
Chloride Attack.
Carbonation.
Corrosion of Inset Steelwork.
Biological Attack.
Degradation of concrete by environmental action is termed, Weathering.
Alkali-Aggregate Reaction (AAR).
Aggregate containing silica will undergo alkalisilica reaction, this forms a gel & begins to absorb water.
The gel swells & exerts a pressure within the concrete.
Gel may weep from the surface of the concrete, termed Exudation, can lead to spalling.
Sulphate Attack.
Seawater contains sulphates, if allowed to penetrate into the concrete, will react with the hydrated cement to form a
crystalline solid (Ettringite).
This causes expansion, leading to cracking & spalling.
Chloride Attack.
If seawater seeps next to the reinforcement within concrete, Chlorides will destroy the passive Fe2O3 skin.
This initialises the reinforcement corrosion process, resulting in cracking & spalling.
Carbonation.
If atmospheric CO2 reaches the reinforcement within the concrete, passivation will be lost.
This will result in reinforcement corrosion, cracking & spalling Biological Attack.
Under Anaerobic conditions, sulphate-reducing bacteria living in the small voids in the concrete, produce H2S.
Some of the H2S may be captured by aerobic bacteria, that oxidise it to form Sulphuric Acid.
This dissolves away the carbonates from the cement & weakens the material, leading to cracking & spalling.
Corrosion of Inset Steelwork.
More likely than reinforcement corrosion.
Different types of steel components cast into the structure - riser clamps - steel skirts - towing eyes.
Should any of this be in contact with the internal reinforcement, the exposed steelwork acts as an anode & the
reinforcement becomes the cathode.
The U.K. Government has published an Offshore Technology Report that categorises 26
Imperfections that may be seen on concrete structures.
This report defines three categories:
Category A – Defects.
Category B - Areas of Concern.
Category C – Blemishes.
Each of these may be either, Construction or Inservice
Category A (Defects).
Usually require detailed investigation & are likely to generate an intervention to repair.
Crack.
Impact Damage.
Popout.
Delamination.
Variable Cover.
Exposed Reinforcement.
Tearing.
Poor Repair.
Tearing Premature movement of the shutter or slumping of the concrete whilst in a semi-liquid state Construction
Poor Repair Showing multiple defects In-Service
Regular Horizontal Ridges.
Concrete bulges slightly as it departs the lower skirt.
Irregular Horizontal Ridges.
Minor variations in the construction process & material.
Construction
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General Cracking:
Well-defined cracks, length, width & shape is apparent.
Pattern Cracking:
Forms a network best described by pattern & area.
When describing the width of cracks:
Fine cracks: < 1mm
Medium cracks: 1 to 2mm
Wide cracks: > 2mm
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Section 6
Marine Growth
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6 Marine Growth
Once any structure is placed into the sea, planktonic marine growth will colonise it. This
build-up will have two effects:
1 The profile area of any component presented to the water flow will be increased. This
will increase the force on the structure overall.
2 Marine growth will change the texture of the surface from a smooth, round steel or
painted surface, to a surface made much rougher by the presence of the marine growth
on it. This roughness will increase with time as the surface becomes more irregular due
to parts of the dead marine growth sloughing off. The effect of this is to increase the
Drag Coefficient.
Both these effects increase the force on the structure. Information on the types and
amounts of marine growth build-up is required to confirm or modify the design-
predicted loads on the structure (Figure 6.1).
Figure 6.1
These two effects of marine growth will have a knock-on effect on the structure that will
manifest itself by:
Producing an increase in mass without any significant change in stiffness.
This causes a reduction in the structure’s natural frequency.
Increasing the mass, there will be added slam effect and drag forces on the
structure. Marine growth, being most abundant (adj) غزيرة- وفيرةat and just below the
water level, coincides (v) يتطابق- يتزامن – يتوافقwith the zone of maximum wave and water
force. Therefore, the effects on the structure are increased in the region of maximum
water force.
Affecting the corrosion rate, either by accelerating or retarding it.
Reducing the effective area of the service inlets and outlets, hence reducing system
efficiency.
Obscuring the important features on the structure, such as diver orientation marks,
valve handles, anodes and similar objects.
Making inspection impossible before cleaning.
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The area between the surface and approximately 20m is known as the Photic Zone.
Below the Photic zone plants will not flourish.
Figure 6.14 gives a generally accepted representation of the combined effects of weight
and volume on the various types of marine fouling in British waters. This should be read
in conjunction with Table 6.1
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6.2.2 Temperature
A rise in water temperature will increase the growth rate of a colony; the growth rate
approximately doubles with a 10°C rise in temperature. There will of course be a limit
and most organisms cease growth at 30-35°C. As the temperature variation is greatest
near the surface, there is seasonal growth in the marine colonies near the surface and
continuous, slower growth as the depth increases.
6.2.3 Water current
The speed at which the water flows over the surface plays an important part in the type
of fouling colony that develops. There are two aspects to consider, the first being that of
the larvae attaching themselves to the structure.
1st aspect: Many larvae are unable to attach themselves at speeds greater than 1
knot. However, once attached, most fouling can withstand water currents of more than
6 knots.
The larvae can attach themselves to structures during slack flow periods, or in localised
spots of slower flow or dead water, such as crevices and locations between hard fouling.
2nd aspect: a strong current brings more food and growth is accelerated.
6.2.4 Salinity
In nearly fresh water, fouling is usually confined to algal slime. As the salinity
increases, so the amount and type of fouling increases. First hydroids and barnacles and
finally mussels occur. The normal salinity of seawater is about 3-3.5% and the size of
mussels, for example, increases five-fold from a salinity of 0.6-3.5%.
6.2.5 Food supply
Growth of the fouling is obviously dependent on the quantity of nutriment available.
Growth rates seem to be faster in coastal waters than those a few miles offshore
where the water is deeper. Investigations suggest that the slow currents that circulate
around platforms become enriched with nutriments from sewage and other waste that
will increase the growth rate.
6.2.6 Cathodic protection
In impressed current, on a limited amount of evidence, the marine growth rate is
increased.
77
Currently the mechanism that encourages an increased growth rate is not understood.
More data is required.
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Section 7
Corrosion
78
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7 Corrosion
7.1 Energy considerations in corrosion
Most materials react with their environment to change their structure.
The reaction in metals is called corrosion,
Reaction of Polymers (plastics) degradation
In concrete is named weathering.
Corrosion in metals is defined as the chemical or electrochemical reaction between
a metal and its environment, which leads to one of three consequences:
1 The removal of the metal.
2 The formation of an oxide.
3 The formation of another chemical compound.
This change in the metal will be expected if the thermodynamics (energy state) of the
system is considered.
The First Law of Thermodynamics states:
Energy can neither be created nor destroyed.
As a direct consequence of this law, when spontaneous changes occur they must follow a
rule, which is:
Whenever a spontaneous change occurs it must release free energy from the system
to the surrounding at constant temperature and pressure.
The overall charge on the atom is zero and an atom, so composed, has a negative
charge of electrons equal to the positive charge of the nucleus.
However, electrons can be added to or taken from the group that surrounds each
atom. When this happens, the overall charge on the atom is no longer zero. This
condition of the atom is called ionic.
If the atom loses an electron it becomes a positive ion, and the atom now has a
positive charge.
If the atom gains an electron it becomes a negative ion and now has a negative
charge.
The first step in the corrosion process is that metal atoms change their state from being
metallic (that is no charge on the atom) to being ionic (that is having a charge on the
atom) by losing at least one electron from the outer shell. The process of corrosion then
goes on at the atomic level, each atom losing one or more (usually no more than three)
electrons to become an ion.
7.3 The anodic reaction
The reaction in which the metal is changed from its metallic state to its ionic state is
known as the anodic reaction. It is part of an overall reaction involving the metal and
other species present in the environment. This process is also called oxidation.
The anodic reaction for iron releases two electrons, as shown in figure 7.3 which
represents a freely rusting iron surface immersed in seawater (the electrolyte).
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This is one part of the reaction in electrochemical corrosion that takes place in the
presence of an electrolyte; that is often water or a water-based solution of ionic
compounds, such as acids, bases or salts. The metal ion passes into solution and the
electron passes through the metal, that is not actually being corroded, that is; an electric
current flows as indicated in Figure 7.4.
The cathodic reaction
These free electrons, formed in the anode reaction, must be used up if the reaction is to
proceed. This part of the reaction in the electrochemical corrosion process, therefore
takes place at the site where the free electrons are neutralised and is known as the
cathodic reaction. Alternatively, reactions such as this that consume electrons are also
known as reduction reactions.
Typically, a complete reaction is for the free electrons to be taken up by positive ions and
atoms of oxygen in the electrolyte. This gives the oxygen a negative charge. Oxygen,
however, readily accepts the free electrons because its electron stability needs eight
electrons in its outer valence shell, yet occurs naturally with only six.
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Free electrons move through the metal cathode to its surface where negative ions form
and subsequently emit free electrons into the electrolyte where they combine with
elements creating different compounds. The site of this reaction is known as the
cathode.
The actual reduction reaction at the cathode will vary according to the composition of the
electrolyte. Hydrogen evolution is a common reaction when the electrolyte is acidic.
Oxygen reduction is also very common, since any aqueous solution in contact with air is
capable of producing this reaction.
It is, of course, the reaction encountered in seawater. Metal ion reduction is less common
and is normally found in chemical process streams. The common denominator with all
these reactions is that they consume electrons and this is the most important point to
note.
7.4 Electrochemical aspects of corrosion
A fundamental definition for corrosion is:
Corrosion is the degradation of a metal by an electrochemical reaction with its
environment.
For corrosion to take place four criteria must apply:
1 There must be an anode: This normally corrodes by loss of electrons.
2 There must be a cathode: This does not normally corrode.
3 There must be an electrolyte: This is the name given to a solution that conducts
electricity.
4 Pure distilled water is not an electrolyte while seawater is.
5 There must be an electrical connection between the anode and the cathode for the free
electrons to travel along.
These four elements are shown diagrammatically in Figure 7.7 and all electrochemical
corrosion takes place by setting up cells like this.
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As this is an electrochemical reaction and the chemistry has been touched on already a
few basic electrical definitions will round off this section.
7.5 Electric theory
Electricity is the passage of electrons between two defined points. This normally occurs
through a metal wire connecting the two points and is called a current.
Electricity can also pass through suitable aqueous solutions but the electrical charge is
then carried by ions.
The amount of charge carried by an electron is known and when a given electron flow is
passed at a constant rate it is measured in amperes and is given the symbol I.
In the MKS (metre, kilogram, second) system, one ampere is defined as that constant
current which, if maintained in each of two infinitely long straight parallel wires of
negligible cross-section; placed one metre apart, in a vacuum, will produce between the
wires a force of 2 x 10-7 Newtons per metre length.
The driving force causing this current to flow is the potential difference between two
points and is measured in volts, which has the symbol V.
In the MKS system this is defined as that difference of electrical potential between two
points of a wire carrying a constant current of 1 ampere when the power dissipation
between those points is 1 watt.
The flow of an electric charge is impeded by a quantity called resistance and between
any two points there is always some resistance to the passage of the current. The unit of
resistance is the ohm which has the symbol Ω.
The MKS system defines the unit of electrical resistance as being the resistance
between two points of a conductor when a constant potential difference of 1V, applied
between these points, produces in the conductor a current of 1A.
During the majority of this section all discussion and illustrations will be in terms of
electron or ion flow and as far as possible, positive and negative notations will be
avoided so as to avoid confusion, which often occurs when corrosion is studied.
This confusion arises because of an historical accident that resulted in producing what is
now called conventional current. Electron flow is exactly opposite to conventional
current, this is what causes the confusion as studies in corrosion so often involve
discussion on electron or ion flow.
To avoid such problems on corrosion only electron flow will be considered.
Figure 7.8 illustrates the two types of flow.
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Section 8
Types of Corrosion
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8 Types of Corrosion
8.1 Corrosion cells
There is some dissimilarity between the anode and the cathode, such as:
Dissimilar metals. (Galvanic Corrosion)
Dissimilar phases in the grains of the metal.
Dissimilar energy levels between the grain and the grain boundary of the metal.
Dissimilar ion concentrations.
Dissimilar oxygen concentrations.
8.4 Pitting
Pitting is localised corrosion that selectively attacks areas of a metal surface. Once
formed, corrosion pits propagate in the same way as crevice corrosion.
1- Consider the case of a water drop lying on the surface of a sheet of clean mild
steel.
2- The corrosion process initiates uniformly on the surface of the steel under the
water. This consumes oxygen (oxygen depletion layer (طبقة استنزاف االكسجينby
the normal cathode reaction in what is a neutral solution at this stage.
3- This causes an oxygen gradient to form within the water drop. It is obvious that
the wetted area around the water/air interface has more oxygen diffusion
from the air than the centre of the drop.
4- This concentration gradient anodically polarises the central region, which
dissolves.
5- The hydroxyl ions generated in the
centre of the drop at the cathode
diffuse inwards and react with iron
ions diffusing outwards, causing the
deposition ترسيبof insoluble غير قابل
للذوبانcorrosion product around the
depression, or pit.
مما يؤدى الى ترسب منتجات التاكل غير القابلة
للذوبان حول الpit .
6- This further retards تاخرthe diffusion
of oxygen, accelerates the anodic
process in the centre of the drop and
causes the reaction to be
autocatalytic. ذاتى التحفيز
Depending on the alloy system and corroding combination, the cracking can be
intergranular or trans granular. SCC cracks have the appearance of a brittle
mechanical fracture, which is readily observed in a scanning electron microscope, Figure
Material /Environment
Brass /Ammonia
Austenitic stainless steels /Chloride-containing solutions
High strength steels /Hydrogen
There are many similarities between corrosion fatigue and stress corrosion cracking, but
the most significant difference is that corrosion fatigue is under dynamic stress,
whereas SCC is under static stress.
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Fatigue affects all metals causing failure at stress levels well below the UTS. (ultimate
stress)
In aqueous environments it is frequently found that a metal’s fatigue resistance is
reduced, or even that it no longer has a fatigue limit.
Summarising the stages in the development of a fatigue crack yields:
Firstly the formation of slip bands.
Next very small cracks form in the order of 10nm long.
Then the extension of this crack along favourable paths.
Finally, macroscopic, 0.1 to 1mm crack propagation; in a direction at right angles to the
maximum principal stress that leads to failure.
Corrosion fatigue can occur in any of the three states indicated by the Pourbaix
Diagram. It can also occur at stress levels much lower than those for stress corrosion
cracking (SCC). It is also true that, while SCC growth rates are independent of the stress
intensity factor during much of the crack growth, fatigue crack growth is always effected
by it.
It is thought that the use of cathodic protection systems that place the metal in the
immune state and over time cause calcareous deposits to form, tend to inhibit تمنع
crack growth, ensuring that the structures are resistant to corrosion fatigue.
8.9 Erosion corrosion
A metal is being attacked because of the relative motion between an electrolyte and a
metal surface, which accelerates the rate of corrosion.
Examples of this type of corrosion are attributable المنسوبةto mechanical effects, such
as, wear, abrasion and scouring.
Soft metals, such as copper, brass, pure aluminium and lead are particularly vulnerable.
عرضة لهذا التاكل
Two main forms of erosion corrosion are:
1 Corrosion associated with laminar (رقائقfluid) flow.
2 Damage caused by impingement أصطدامin turbulent conditions.
A laminar flow will cause several effects:
Where the increased flow replenishes يجددaggressive عنيفions, such as chloride and
sulphide, this has a detrimental ضارeffect and corrosion rates increase.
If the flow contains any solid particles, protective layers may be scoured away causing
excessive corrosion.
The alternative to this is that it is sometimes possible in pipes for the deposit of silt to
be prevented, thus preventing the formation of any differential-aeration cells in the
crevices beneath.
A possible beneficial effect is that more oxygen is carried to the area, which minimises
the formation of differential-aeration cells that are normally a common cause of attack.
Another possible beneficial effect is where a steady supply of inhibitor is concentrated
within the flow, as in a pipeline for example.
These combined circumstances make the effects of laminar flow unpredictable.
Taking the case of turbulent flow, however, the situation is much more straightforward.
The fluid molecules now impinge directly on the metal causing wear. This obviously
increases the corrosion rate.
This effect can easily occur inside a pipe
because turbulence can be caused by sudden
changes in bore diameter, or direction:
(ie pipe bends), a badly fitted joint or gasket,
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The reaction of sulphate-reducing bacteria (SRB) under anaerobic (no oxygen present)
conditions.
- The most important of these are the bacteria Sporovibrio desulphuricans. These
thrive نما-تزدهرin the reduced oxygen conditions created under heavy accumulations of
marine growth, under thick deposits of corrosion products, or under mud.
- There are indications that, because oxygen is unable to diffuse through the heavy
marine growth, the effect of this organism is to take the place of oxygen in the usual
cathodic reaction.
By the formation of concentration cells around and under the organisms.
91
Fretting corrosion may also occur due to the continued movement of hard shelled
(mussels) creatures on the structure’s surface.
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8.12 Temperature
Most chemical reactions are speeded up by an increase in temperature. Hot risers,
exhaust and cooling-water dumps are all sites that can and do corrode more quickly than
other sections of offshore structures. Therefore, these components being more
susceptible must be inspected more regularly.
8.13 Water flow rate
In general, if the water flow is increased then the rate at which the metal is removed is
also increased. If there is impingement of the flow on the metal or aeration takes place
near the surface, then a very much larger rate of metal removal is experienced locally.
The pitting of ship’s propellers and pump and dredger impellers are general
examples of this.
8.14 The pH value of the water
The corrosion rate of metals is directly affected by the pH value of the electrolyte. Steel,
for example, corrodes least when in a solution that has a pH of between 11 and 12.
Water is a neutral molecule in which two atoms of hydrogen combine with one atom of
oxygen (H2O). There is a limited amount of dissociation ( انفصالseparation of positive
and negative charged ions in solution) into Hydrogen ions H+ and Hydroxyl ions OH.
Water represents a neutral substance as it contains both acid H + and alkali OH in equal
amounts.
This can be noted in the form of an equilibrium:
H2O is H+ + OH relationship between these elements forms the basis of a scale of
acidity.
All acids have one common property: that is the presence in aqueous مائىsolution of the
Hydrogen ion, whereas, alkali has Hydroxyl ions.
The opposite of acid is alkali (basic), which means that acids are neutralised by alkalis
The method of defining acidity is by means of a term called pH, which indicates the
amount of hydrogen activity. It is measured on a scale of 0-14.
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Section 9
Corrosion Protection
93
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9 Corrosion Protection
There are numerous methods for preventing corrosion including, coatings, inhibitors
(controlling the electrolyte), selective design, anodic protection and cathodic protection.
Before considering these methods a brief examination of the way in which the corrosion
process is influenced by the two main variables;
The electrode potential and the pH value will assist in understanding the various
protection methods.
These data are often presented in diagrammatic form known as Pourbaix Diagrams.
These diagrams are obtained from laboratory tests carried out under controlled
conditions of constant temperature and no flow.
There are three distinct possible states of corrosion depending on electrode potentials
and pH values:
Corrosion
At intermediate electrode potentials and over a very wide range of pH values corrosion
takes place and metal is removed.
Passivity
At higher electrode potentials and over a wide range of pH values, there is a passivity
region. This is the region in which a corrosion product film is formed, that in most cases
is an oxide film. It is worth noting that the diagram only indicates that an oxide film is
formed; it does not mean that the oxide film gives protection. The properties of the
film must be known in order to determine this.
Immunity
At low electrode potentials and over almost the whole of the pH range, the rate of
corrosion is so low that the metal is said to be immune.
9.1 Cathodic protection
Apart from the three stages indicated by Figure 9.0 it is also possible to determine basic
strategies for preventing corrosion.
Making the electrode potential more positive will produce passivation at point B.
Making the electrode potential more negative will produce immunity at point C.
Making the electrolyte more basic (Alkali) will produce passivation at point D.
acceptable corrosion rate. This level of current density will ensure the required
corrosion rate is achieved. All that remains is to read off from the graph the value of the
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the sacrificial system in that the structure is made to be the cathode. However in the
case of the ICCP system the necessary potential and current flow is provided by a DC
generator rather than by a galvanic coupling.
This system can be made to be self-adjusting by incorporating reference electrodes
into the circuit that measure potential. The potential can vary depending on the
circumstances; if the structure has a coating initially that in subsequent service becomes
damaged this will increase the exposed surface area needing to be protected. The
control unit can deal with this by increasing the current density. If on the other hand
there were a reduction in the surface area; as for instance a calcareous deposit building
up, there would be less surface area exposed and the current requirement would be less.
In both cases the reference electrode provides the means of monitoring the potential,
which varies proportionally according to the current.
Table 9.1 Advantages and disadvantages of ICCP.
The anode material is selected from the top of the Galvanic Series not the bottom.
Materials such as titanium, platinised niobium and lead/silver alloys are used.
The anode and supply cables are insulated from the structure to prevent any of the
problems associated with over-protection.
Noble metals, virtually non-consumable anodes, can be used in this system because
in electrolytes of pH 7 or less the anode reaction is the oxidation of water, rather than
metal dissolution:
2H2O = O2 + 4H+ + 4e-
In electrolytes of pH values greater than 7 (alkaline solutions) the reaction is the
oxidation of Hydroxyl ions:
4OH- O2 + 2H2O + 4e-
In seawater the reaction is usually oxidation of chloride ions to chloride gas:
2Cl- Cl2 + 2e
As indicated above the actual distribution of the anodes on any structure may be either:
Platform based
Here numerous anodes are attached to the structure at intervals around it in similar
fashion to sacrificial anodes but ensuring that they are insulated from the structure.
Figure 9.2 refers.
Two problems are associated with this method. One is the possibility of shadow areas
where inadequate protection is provided. This problem can be solved by the use of
sacrificial anodes complementing the ICCP system as indicated earlier.
The second problem is the possibility of current flowing directly from the anode to the
adjacent structure. This could cause embrittlement as discussed earlier and to avoid
this dielectric shields are employed to insulate the structure electrically. Also the
current is limited by design because each anode is positioned to provide adequate
protection for the local area only. This limits as well the possibility of embrittlement and
coating damage. See Figure 9.3
There is also a diver safety consideration in that these anodes are at about 80V potential
with some 1000A current. If divers are employed adjacent to any of the anodes they
should be isolated from the system.
Remote from the structure
A number of anodes may be placed on the seabed at a designated distance from the
structure.
97
This method avoids the possibility of current flowing directly from the anode to the
adjacent structure but there being fewer anodes the current density is higher and
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Reference or control electrodes are vital components of any ICCP system. They
determine the current required from the power source, without these items the system
cannot provide a quantifiable degree of protection. Figure 9.5 refers.
Spray coats utilise a specialised torch that is fed with wires of the coating metal that
are melted and blown out by it. The molten metal is expressed in the form of
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droplets travelling at 100-150m s-1 that flatten and adhere on impact with the
component Cladding uses metal skins laminated onto the component. The skin can be
applied by.
Rolling.
Explosive welding.
Buttering (building up a welded coat on the
surface to be protected).
Sheathing.
Aluminium roll-bonded to duralumin is marketed
as Alcad. Some offshore risers are sheathed with
monel (cupronickel) See Figure 9.7.
Diffusion requires the component to be heated to
just below the melting point of the coating metal
in the presence of the coating in powder form and in
an inert atmosphere. The component is allowed to
baste for several hours and the coating diffuses
into the surface of the component.
9.5 Inhibitors (controlling the electrolyte)
Remember the Pourbaix diagram indicates three
methods for preventing corrosion:
Making the electrode more positive.
Making the electrode more negative.
Changing the electrolyte pH.
This section will outline methods for changing the electrolyte.
Also remember there are four processes in metal corrosion:
The anodic reaction.
The cathodic reaction.
Ionic conduction through the electrolyte.
Electron conduction through the metal.
Only the first three are affected by the electrolyte, electron conduction through the
metal is not considered here. The properties of the electrolyte that can be affected by
using inhibitors are:
Conductivity of the electrolyte.
pH of the electrolyte.
Interaction of the electrolyte with the metal surface, attacking or strengthening
passive films.
As an example of how this can be achieved consider steel in seawater. If distilled water is
substituted for the seawater the conductivity and pH of the electrolyte is reduced and a
passive film will form on the surface of the steel.
9.6 Corrosion protection by design
The methods employed to protect structures from corrosion can be summarized thus:
Avoid all unnecessary bimetallic corrosion cells.
Avoid differential-aeration cells (crevices, debris traps, poor drainage, etc.).
Avoid stray currents from electrical machinery or conductors.
Choose the material with the best properties for the environment.
9.7 Anodic protection
In this method of corrosion protection a potential is applied to the anode that
maintains it in the passive range of the Pourbaix Diagram. This allows the formation of
a passive film that is robust enough to provide a barrier to the normal corrosion process.
However, this film is unreliable for steel in aqueous solutions and therefore is not used
on offshore structures.
100
Aluminium does form such a film naturally and some types of Aluminium can benefit
from this because the passive layer is sufficiently robust to be relied upon.
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Section 10
Corrosion Protection Monitoring
101
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10 Corrosion Protection Monitoring
Visual inspection and CP survey, ultrasonic thickness surveys, ROV inspection and
intelligence pigging are widely used subsea.
Chemical analyses and solid particle detection of samples collected from the pipeline at
the topsides will provide corrosion information to assess both topsides and subsea
pipelines.
The amount of current from sacrificial anodes or from an impressed current system
required for protection varies:
From metal to metal.
With the geometry of the structure.
With differences in sea water environment (temperature, pH value, etc).
With any other factors that affects the resistance of the circuit.
Since the amount of current required for the protection of any structure cannot be
accurately predicted or distributed evenly through the structure, the method of checking
for adequate protection is to measure the potential and current density around the
structure at various places.
10.1 Inspection requirements
Monitoring or inspection requirements for corrosion protection systems are therefore as
follows:
Visual inspections of both sacrificial and impressed current anodes for depletion.
Visual inspection of the electrical connections of the sacrificial system to see that it is
intact and of the impressed current system to ensure that there are no breaks in the
insulation of the supply cables or anode connections.
Potential measurements on the structure to confirm that it is still the cathode by
confirming the readings obtained are within protection parameters. (-800mV to -1100mV
generally).
Current density measurements to confirm that the impressed current system is
providing adequate protection.
Visual and ultrasonic inspection for corrosion damage including pitting and loss of wall
thickness.
The potential measurements usually referred to as cathode potential (CP) readings
are obtained by:
Taking contact readings with a CP meter:
Silver/silver-chloride (Ag/AgCl).
Copper/copper-sulphate (CSE) (this is more favoured for concrete structures).
10.3 High purity zinc electrodes (ZRE)
High purity zinc (99.9% pure) is most commonly used with remotely mounted monitoring
systems as shown in section 9, figure 9.6. The site for mounting the electrode is selected
because it is either a representative site, it is an area of marginal protection or it is an
area of high stress and it is installed as part of the impressed current system. The
electrode is connected to a meter in the surface control room.
10.5
up a visual inspection that had identified more corrosion than was anticipated. Specific
procedures will be provided for this type of survey.
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A monitored anode is a sacrificial anode that is
isolated electrically from the structure and is
connected via an insulated cable to the
surface control room. Thus the current can be
constantly monitored.
10.8 Procedure
The first part of the procedure proves that the K-series cells are chemically saturated and
sufficiently stable enough to be used as reference cells.
10.8.1 Proving the K-series cells
There are different types of cells available. One type is specifically designed for use with
a Bathycorrometer. This type has a solid polymer body protecting the K-series cell.
The procedure outlined below also applies to this type of cell; however, it is not
possible to visually confirm they are fully saturated with solution. They are sealed and
to confirm they are saturated, it is necessary to unscrew a sealing cap to gain access to
the solution reservoir.
Visually inspect the electrodes to ensure they are undamaged and full of solution. The
solution is potassium chloride (KCl) and if the solution is saturated or supersaturated
solid crystals may be seen in the phial.
(Commonly the phials are glass or clear plastic).
Label the electrodes and their wires 1, 2 and 3.
Soak the electrodes in the bucket for 24 hours, being careful to immerse each one only
as far as the filling hole in the phial.
While the electrodes continue to soak connect electrode 1 to the negative terminal of
the voltmeter and electrode, 2 to the positive terminal and record the reading.
Repeat the test with each permutation of electrodes.
1 and 3 & 2 and 3
Acceptable readings between any pair of electrodes is 0 ± 2MV.
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If all the readings are within this range any electrode may be used.
If one reading is out of this range the electrode not in that pair is the one to use.
If one reading is in range either of the electrodes in that pair can be used.
If all of the readings are out of range either replace all the K-series cells or flush out
the phials with pure distilled water, obtain a new saturated solution of potassium
chloride, refill the phials and re-test.
On completion of the entire procedure rinse the electrodes in fresh water.
The second part of the procedure confirms the calibration of the CP meter.
10.9 Calibration of the meter
The calibration procedure for a contact CP meter is basically the same whether
it is diver hand-held or ROV deployed.
10.9.1 Calibration of a Bathycorrometer
The calibration checking procedure is slightly different if the meter being calibrated is a
Bathycorrometer with the specifically designed screw-on cells. In this case the following
procedure applies.
As the electronic components in the Bathycorrometer can affect calibration it is
necessary to use a BCM Checker (supplied separately by the manufacturer) to check
there are no electrical faults in the unit before continuing with this procedure.
Separate instructions are supplied with this equipment so will not be detailed here.
Once satisfied that the electrical components are functioning correctly:
Fully charge the CP meter batteries and soak in fresh seawater (not drawn from the fire
main).
Remove the contact probe tip and white Delrin probe cone from the meter.
Screw the K-series reference electrode onto the Bathycorrometer in place of the Delrin
probe and probe cone tip.
Immerse the meter in the bucket at least far enough to submerge the semipermeable
membrane. Gently shake the unit to remove any air bubbles lodged in the holes. (The
meter display may be left out of the water to assist taking readings).
Allow time for the meter to stabilise (approximately 10 minutes).
The voltage potential between the reference electrode and the meter’s own Ag/AgCl
cell is read off the meter display directly.
Record the reading on the log.
Acceptable readings are +42mV +/-5mV. It should be noted that values will vary
dependent upon salinity and temperature of the seawater, see Figure 10.7
The calibration of other types of contact CP meters is by comparison.
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Note. If the reference electrodes used are Calomel cells (as opposed to Kseries) then
the expected reading will be 0 to - 10mV.
10.10 Operating procedures
To ensure that accuracy is maintained and that repeatable results are obtained,
CP monitoring methods should follow a procedure as follows.
Ensure any self-contained meters are fully charged and maintain a battery charging log.
(Usual requirements for charging batteries for battery operated equipment are 15 hours
from fully discharged. This will give 60 hours of continuous use).
Ensure the probe tip for contact meters is sharp (hand-held meters are usually supplied
with spare tips).
Soak meters and half-cells for a minimum of 30 minutes before use. (This allows time
for ion penetration through the semi-permeable membranes.)
Confirm the calibration of the system in use according to the appropriate calibration
procedure. Record the results on the appropriate log sheet.
Record meter serial number and any other specified details on the appropriate log
sheet.
Take a reference reading on zinc at the inspection site prior to starting the survey.
For each contact readings ensure there is correct metal-to-metal contact between the
probe tip and the cathode surface.
With proximity probe surveys ensure there is a solid electrical connection to the
structure connected to the positive terminal of the surface instrument.
For proximity probe readings ensure the standoff between the probe and the cathode is
correct, no more than 100mm away.
During the course of the survey ensure that each reading is correctly recorded on the
appropriate log.
On completion of the survey take another reference reading on zinc.
Recover the equipment, wash in fresh water, dry and store. Charge any battery-
operated equipment as necessary and complete the battery charging log.
Notes:
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Like MIG/MAG, TIG can also be used with different shielding gases:
Argon
For stainless steel, high carbon steel, aluminium and magnesium.
Helium/Argon mixes
For carbon steel, stainless steel, aluminium, copper and magnesium.
Variations
Include adding nitrogen to helium/argon mixes for welding copper and adding
hydrogen to helium/argon mixes for welding austenitic stainless steels.
Common faults associated with TIG welding are:
Excessive penetration - Arc strikes - Burn through - Incomplete penetration.
Tungsten inclusion – Porosity – Undercut - Oxide inclusions.
is particularly useful for welding thick steel sections and used extensively where long
continuous weld runs are to be made. The following photographs and drawings best
illustrate the equipment and process.
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The flux is in the form of powder or
granules continually fed over the work
area and the electric arc is formed
underneath so is totally submerged,
giving the process its name. Because of
this, personnel do not need eye protection
as the arc is not visible.
The process uses amperages in the range
of 100-2000amps, giving very high
current density to the electrode wire,
which produces the deep penetration and
weld dilution needed for thick section
steel.
11.8 Types of welded joint
There are approximately 110 different welded joint variations; the majority of which are
not seen in the construction of offshore structures. So it is necessary to have knowledge
of only five types of joint.
11.8.1 The butt joint - (not to be confused with a butt weld!)
The two components that make up this joint are fitted together end to end at an angle
of between 135-180°. This joint is used to join pipe sections end to end, welding plates
together and numerous other applications (Figure 11.11).
11.8.2 T Joint
The two components are fitted together at an angle of 5-90°. This configuration is found
on offshore jackets at nodes and in numerous other areas (Figure 11.12).
11.8.3 Lap joint
The two components are fitted one on top of the other. The angle between them is 0-5°
(Figure 11.13).
11.8.4 Corner joint
The two components are connected at the ends to make a joint at an angle between 30-
135° (Figure 11.14).
11.8.5 Cruciform joint
Joint made by welding two components to a third at right angles, on the same axis, on
opposite sides of the third component to form the shape of a cross (Figure 11.15).
As fillet welds are not used for structural joints that must withstand high stresses, the
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butt weld will be the type of weld most frequently inspected offshore. All nodes,
including any safety critical nodes on the structure, will be constructed using butt
welds.
11.10 Welding metallurgy علم المعادن
The mechanism by which welding takes place must be understood to achieve a weld
remains for design life of the structure.
The prime factor in welding is temperature. The various welding processes, types of
weld and types of joint are all designed so that the heat generated during the welding
process can be dissipated تبددuniformly as the molten metal cools after the weld metal is
deposited. Figure 11.17 shows how this occurs.
At point 1 within the molten weld pool, the temperature will be above the melting point
of the filler rod metal. The welding current and technique of the welder determine this
temperature.
The main heat flow away from the weld pool will be along the parent plate.
Between points 1 and 2, the temperature must raise above the parent metal melting
temperature so that fusion (ie melting the parent plate and mixing with the weld pool
metal), occurs.
This region (between points 1 and 2), is known as the fusion zone and can be readily
seen if a sample of the weld is sectioned, polished and etched.
The temperature then reduces from point 2-3, which is a region of the parent metal that
has sufficient heat input to cause grain structure modification, known as the heat
affected zone (HAZ).
HAZ
One of the means of making a material softer (often called annealing) is to heat it up
and allow it to cool slowly. A common example of this is copper pipes for domestic water
systems that are softened in this way in order to bend them to required shapes.
To achieve this softening effect a material has to be heated above its re-crystallisation
temperature (Trecry). Above this temperature, grains in the material will reform and
grow.
In Figure 11.17 this temperature is reached at point 3, so that the material between point
2 and 3 that has been raised above the re-crystallisation temperature will be liable to a
change of properties. This region can also be seen on a polished and etched sample of
the weld.
The temperature continues to fall between points 3 and 4, which is ambient temperature.
Figure 11.17 only shows what is happening along the line AA; but this happens
throughout the section. This leads to the different regions of the weld, as shown in Figure
11.18 and is a graphic indication of the way temperature gradients have to be managed
112
in any weld.
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This temperature management is as important for cooling as it is for heat energy input
into the weld. The cooling rate must be as controlled as the heat flow during the actual
welding. In general, fast cooling rates (often referred to as quenching), make the
material harder. In steel, this comes about by the formation of a structure known as
Martensite. Martensitic steel has a grain structure arranged in a regular lattice, which
makes the steel hard and less tough (ie less able to withstand crack propagation).
Note: If the cooling rate is not properly controlled and the material is allowed to quench,
it has the opposite effect to annealing outlined above.
11.11 Further considerations for weld control
While heat input and cooling rate control may be of paramount importance to the
finished quality of a weld, there are several other factors that must also be considered.
Defects, such as porosity, often arise in welds due to gas penetrating the weld pool
protection. Gases that are likely to be present in the weld are hydrogen, oxygen and
nitrogen. These are derived from the atmosphere, water, hydrocarbons (usually in the
form of grease and oil) and other oxides present in the vicinity of the weld because of a
lack of care in preparation, بسبب نقص االعدادnot ensuring that the weld area is clean and
dry.
These products get into the arc and provide a supply of gas that can be dissolved in the
liquid metal of the weld pool. On cooling, the solubility of the dissolved gas in metal
reduces and the gas comes out of solution to form bubbles trapped in the weld metal;
or sometimes, the gas diffuses into the parent metal. Hydrogen diffusing into the HAZ
will cause hydrogen embrittlement, which may lead to cracking.
The different temperatures in the regions around the weld will cause differential
expansion. On cooling, if cracking does not immediately occur in the weld or in the HAZ,
the material is put under a permanent stress, unless a stress relieving procedure is
specified. This state of stress is referred to as residual stress.
Normal working stress is imposed on top of and in addition to this residual stress, giving
an in-service stress that is higher than the normal design working stress. The effect of
residual stresses will be, at the very least, a reduction in the fatigue life of the joint. At
the moment, there is no way that these residual stresses can be measured during the
course of a routine inspection. (Alternating current field measurement (ACFM) may be
developed for this purpose).
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Filler bead
When the weld is made up of more than one pass of a filler rod the successive
passes are called filler beads.
Run or pass
Weld metal laid down in a single pass from a filler rod.
Weldment
An alternative term to describe the weld zone.
Fusion zone
The edge of the parent plate along the prepared face and the root face along
which the weld metal fuses with the parent plate.
Root bead
Weld bead laid into the root that protrudes beyond the back wall of the parent plate.
Run out length
The specified maximum lengths of weld run for a particular rod type.
In this case the International Institute of Welding (IIW) and BS EN ISO 5817:
2007 apply. In the same way that welding terms are defined in this standard, weld defect
terminology is also defined.
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Volumetric defects
Inclusions, porosity and other internal flaws, that have a large volume compared to
surface area, are in this category. They are 3-dimensional and will also include undercut
and lack of penetration. This category of defect is caused during fabrication, not in-
service.
Only a certain number of these standard terms apply to defects that may be found on
the surface of the weld accessible to the underwater inspector.
11.17 Cracks
These are linear discontinuities produced by fracture, cracks may be:
Longitudinal
- Transverse
- Crater
- Centreline
- Toe
- HAZ.
11.18 Cavities
A number of flaws are covered by this category.
Porosity: Linear or cluster
Gas pores that may be located in different locations.
Elongated cavities
A string of gas pores parallel to the weld axis.
Shrinkage cavity
A cavity caused by shrinkage of the weld metal while it is in a plastic state.
Crater
A depression caused by shrinkage at the end of a run if the heat is removed quickly.
117
Crater pipe
A hole in the centre of a crater, caused by shrinkage.
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11.19 Solid inclusions
Volumetric defects caused by solids trapped in the
weld pool before it solidifies.
11.20 Lack of fusion and penetration
Lack of fusion
The weld metal has not bonded.
Lack of sidewall fusion
No union between the weld metal and the parent
plate.
Lack of root fusion
No bonding at the root of the weld joint.
Incomplete root penetration
No weld metal extending into the root of the weld.
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11.21 Imperfect shapes
Excess weld metal
Weld metal lying outside the plane joining the toes.
Excess penetration
Excess weld metal protruding through the root.
Root concavity
A shallow groove in the root.
Incompletely filled groove
A groove caused by insufficient weld metal being laid onto the cap.
Undercut
A groove in the toe of the weld where the parent plate is gouged due to the welding
current.
Overlap
Weld metal spilled over from the cap onto the parent plate outside the line of the toe
that has not fused with the parent metal.
Burn through
This is a collapse in the weld pool caused by excessive penetration resulting in a hole in
the weld.
Unequal leg length
Not a standard term but internationally understood,
describing different leg lengths on a fillet weld, usually
a T joint.
Poor restart or poor stop/start
Not standard terms but internationally understood, an
irregular start or pick-up after one bead is ended or
interrupted and the next arc strike is imperfectly
aligned with the previous bead.
Misalignment
(Not a standard term but internationally understood),
poor fit-up resulting in the parent plates being out of
alignment either laterally or angularly.
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11.22 Miscellaneous
Stray flash or arc strike
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Burn marks on the parent metal caused by striking arcs with the welding rod off the line
of the weld; can sometimes be caused by arcing of the weld supply cable if the insulation
is damaged.
Excessive dressing
Grinding away too much weld metal and leaving the weld below the level of the surface
of the parent plate.
Grinding mark
Grooves or marks on the parent
plate caused by poorly controlled
grinding or surfacing tools.
Tool mark
Marks indented into the parent
plate caused by chipping
hammers or similar hand tools.
Hammer mark
Obvious damage caused by a
hammer blow.
Torn surface
Surface irregularity caused by
breaking off temporary
attachments, colloquially known,
though not always accurately, as
dog scars see below.
Surface pitting
Small depressions on the weld or parent plate.
Spatter
Spots of weld metal thrown out from the weld pool and attaching themselves to the
parent plate.
Dog scar - colloquial term, see above
A welding scar left over after removal of a dog, (a temporary metal fixing used to
stabilise the parent plates during the welding process).
11.23 Reporting defects in welds
As diver inspectors are concerned with in-service inspections, volumetric defects will
seldom be identified, as they are usually caused during fabrication.
Planar defects may be observed as these could be caused by stress or fatigue
failure leading to crack-like features becoming evident.
This type of discontinuity will be of most concern in the toe of the weld, which is also
the zone where it is most likely to be found. This is because at this point there is a region
that has been heated and melted causing grain structure changes as outlined earlier.
Also in this area, the geometry of the weld changes, which may create a notch effect;
that is an area where stress is increased above the average for the rest of the
component.
Any defects identified must be reported by recording at least:
1- Type of defect
Describe the defect with correct terminology.
2- Location
State the global location, ie what component is damaged, where on the component the
damage is (state the clock and or tape position relative to a known datum), give the
relative location, ie is it on the HAZ, in the toe, on the weld cap or in the parent plate.
3- Dimensions
State the start position and give length. If the defect is a crack-like feature state whether
it is continuous or branching, the orientation and if it is measurable give width and depth.
4- Description
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The sound wave so produced travels through the air at a speed of about 332m/sec, at
0°C, at sea level. We hear the sound when it hits a membrane in our ear and causes it to
vibrate.
Sound will travel through any medium that has molecules to move, but it travels faster
in more elastic materials because the vibrations are passed on more quickly. Sound
travels faster in water or metal than it does in air, as liquids and solids are more
elastic than air. The speed of sound increases with the stiffness, (elasticity) and
decreases with density, in fact, it’s actually the square root of the stiffness divided by
the density.
12.1.1 Frequency
As sound is a series of vibrations, one way of measuring it is to count the number of
vibrations per second - the frequency. Frequency is measured in Hertz. One vibration in
one second is one Hertz. Two vibrations in one second is two Hertz. Ten vibrations in one
second is 10 Hertz and 1000 vibrations in one second is 1000 Hertz or one kilohertz
(kHz). One million vibrations in one second is one Megahertz (MHz).
The higher the frequency - the higher the note sounds - the higher the pitch.
We can only hear sounds between certain frequencies - more than 16Hz and less than
20,000 Hertz. A dog whistle vibrating at 25,000 Hertz cannot be heard by humans, but
itcan be heard by the sensitive ears of a dog.
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Other animals can hear sounds at higher frequencies - bats can hear sound at 100,000
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Hertz.
A sound with frequencies above the upper range of human hearing 20KHZ is called
ultrasound. Sound below about 16 Hertz is called infrasound.
However, there is an advantage for the lower frequencies. The lower the frequency, the
more penetrating a sound wave is - that is why foghorns give out very low notes and
why the low throbbing notes from your neighbour’s stereo come through the wall rather
than the high notes. Elephants and hippos can communicate over distances of up to 30
kilometres using infrasound.
Practical ultrasonic testing, the frequency range used is between 0.5- 6MHz; the lower
frequencies between 0.5 - 1.5MHz are used for materials with large grain structures,
such as concrete or cast iron. Frequencies from 2 - 6MHz are used for testing
materials with fine grain structures including steel.
12.1.2 Velocity
So far, only the effects of the wave passing one point in the material have been
considered. However, the wave itself is passing through the material. Like a surface wave
on water, the water at any point goes up and down, but as well as this the wave travels
forward.
Ultrasonic waves travel through a material at the speed of sound for a given type of
wave in a given material. That is, the speed of sound is different for different types of
wave and the speed of travel is different in different materials.
12.1.3 Types of ultrasonic waves
Sound waves propagate through a material (liquid, solid or gas) by causing the atoms to
oscillate as the wave front passes through it. There are two types of wave that
propagate through the solid material and three types that travel along the surface
skin of the material.
The three types of surface wave have no application underwater and will not be
discussed further. The two types of wave that propagate through a solid are discussed
below.
Longitudinal/Compression waves
This type of wave is denoted by the symbol L,
with the addition of a letter V – VL we indicate
the velocity of propagation of
longitudinal/compression waves. With this type
of wave propagation, the direction of oscillation
of the atoms is the same as the wave
propagation see Figure 12.3.
Transverse/Shear waves
This type of wave is denoted by the symbol T, with
the addition of a letter V – VT we indicate the
velocity of propagation of these waves. With this
type of wave propagation, the direction of
oscillation of the atoms is at 90o to the wave
propagation see Figure 12.4.
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In order that ultrasonic sound waves can be used to measure depths and sizes within any
material, it is a fundamental principle that the velocity of the sound wave remains
constant for different samples of the same material. This is in fact the case; and
furthermore, the ultrasonic wave obeys the Laws of Light .
A summary of wave velocities of the various waves discussed here for a selection of
materials is shown in table 12.2
Note: Blank spaces in the VT column, this is because Shear waves cannot be produced in
liquids, solids or polymers such as Perspex or concrete.
12.2 Wavelength
A wave in the sea is a vibration of energy. As the wave passes a fixed point it produces
a constant rise and fall of energy.
A complete vibration is a change in energy from maximum to minimum and back to
maximum.
A wavelength is the distance a stress wave moves forward during one complete cycle.
It varies with the speed of sound and with the frequency. Wavelength is represented by
the Greek letter Lambda. We can work out wavelength if we know the speed and
frequency of a sound wave. Wavelength is the velocity in metres per second
divided by the frequency.
If we want to know the wavelength of a 2MHz compression wave travelling through
steel, we can again use the formula, as we know the compressional speed of sound in
steel, 5,940m/sec.
=5,940,000/2,000,000 = 2.97mm
If we want to know the wavelength of a shear wave of 2MHz in steel we can use the
formula again, we use the shear speed of sound in steel which is 3,250m/sec.
An easy way to remember how this formula works is to split it down
within a triangle - with the velocity, wavelength and frequency at the
corners.
If we want to work out wavelength we cover the wavelength symbol –
this leaves the V over ƒ.
The wavelength of an ultrasonic wave is important because the
shorter the wavelength, the smaller the flaws that can be discovered. Defects of a
diameter of less than half a wavelength may not show on the CRT. On the other hand,
the shorter the wavelength the less the ultrasound will penetrate the test material.
12.3 Further effects of ultrasonic properties in materials
As the ultrasonic signal passes through a material, a pressure or stress front will be
initiated in the material, which will present resistance to the passage of the sound wave
energy. The amount of resistance will depend on the properties of the material. This
is a useful parameter of a material and must be determined if the pressure or stress
magnitude of the ultrasonic wave is to be determined.
12.3.1 Acoustic impedance (Z)
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When the angle of incidence is 0°, the reflected angle is also 0°, so the wave is reflected
back along the incident direction. The wave is travelling in the same material; therefore,
there will be no change in wavelength of the signal or the mode of travel of the wave.
This is the ideal condition for thickness measurements using ultrasonic compression
waves.
12.4.2 Law of Refraction (Snell’s Law)
At an interface, part of the ultrasonic wave
is reflected and the rest will pass into the
second material. The path in the second
material will still be straight line, but the
direction of this wave will not be continuous
with the direction of the incident wave as it
will have been turned through an angle that
can be determined by Snell’s Law.
constantly receiving.
The electric isolation is achieved by provision of two co-axial connectors, one for transmit
and one for receive, while the acoustic barrier is generally a thin layer of cork.
A twin crystal probe is designed to minimise the problem of dead zone. A twin crystal
probe has two crystals mounted on perspex shoes angled inwards slightly to focus at
a set distance in the test material. Were the crystals not angled, the pulse would be
reflected straight back into the transmitting crystal.
12.6.6 Couplant
Ultrasonic testing cannot be carried out in air without the use of a suitable
coupling agent between the probe and the test surface. This is because the
mechanical pulses cannot travel across the small air gap that exists between
the two surfaces, because of the mismatch in acoustic impedance between the
shoe of the transducer and the air. For underwater inspection the seawater acts
as a couplant and aids the passage of ultrasound into the material.
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12.7 The sound beam
The spread of sound waves from a Piezo-electric crystal has been likened to the
beam of a torch, an elongated cone. Just as the intensity of light from a torch
diminishes with distance, so sound pulses get weaker the further they travel
from the crystal.
An acoustic sound wave has also previously been described as being a single
sinusoidal wave propagating through a material. These analogies do not
however present a totally true picture.
The sound produced from an ultrasonic crystal does not originate from a single
point but rather it is derived from many points along the surface of the Piezoelectric
crystal. This results in a sound field with many waves interacting or
interfering with each other.
After a time, the shock waves, or pulses, even out to form a continuous front.
The area between the crystal and the point where the wave front evens out is
what we call the Near Zone. Inside the Near Zone signals from a reflector bear
no accurate relation to the size of the reflector, as the sound vibrations are
going in all directions. This affects the accuracy of flaw sizing of small reflectors
inside the Near Zone.
The Near Zone of a crystal varies with the material being tested, but it can be
worked out by a formula:
Near Zone NZ= D2
4
12.8 Principles of ultrasonic testing
There are two basic principles of ultrasonic testing.
The first is based on the detection of a decrease in energy of the ultrasonic
beam due to absorption by the flaw.
As an example of this type of instrument, figure 12.23 shows the control panel
of a Krautkramer USM2
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The ultrasonic flaw detector, the UT set, sends a voltage down a coaxial cable
to the probe. The Piezo-electric crystal in the probe is hit by the voltage and
vibrates. The vibration creates an ultrasonic pulse, which enters the test
material. The pulse travels through the material until it strikes a reflector and is
reflected back to the probe.
It re-enters the probe, hits the crystal and vibrates it, causing it to generate a
voltage. The voltage causes a current which travels back to the flaw detector
along the cable. The set displays the time the pulse has taken through the test
material and back and the strength of the pulse as a signal on the CRT screen.
This is basically how a UT set works. It transmits energy into material via a
probe and measures the time in microseconds that the sound pulse takes to
return to the probe. The controls on the UT set are almost entirely concerned
with presenting a display on the CRT screen for the operator to interpret.
The cathode ray tube is a device for measuring very small periods of time. The
CRT displays electrical pulses on a screen in a linear time/distance relationship.
That is, the longer the distance on the screen time base (the X-axis), the longer
the time that has been measured.
On the Y-axis (vertical) the amplitude of the returning signal is indicated, the
higher the amplitude of this signal, the greater the strength of the reflected
signal. Of course, in the case of thickness measurements this will be the back
wall echo.
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12.9.5 Calibration and reference blocks
A-scan type instruments all require calibration before being used for testing.
Normally calibration will require the use of a calibration block, however a
reference block may be used if this is either specified or agreed by the client.
Reference blocks
These are manufactured for the client to agreed specifications and surface finish
and are used solely for a particular job and are not intended for any other
purpose. This is usually because they are intended for use on specialised steels
that would have different velocities.
Calibration blocks
There is several different calibration blocks available for ultrasonic testing.
The two most popular are; the IIW V1 and IIW V2 calibration blocks. A
calibration block is manufactured to standard specifications and to international
standards. It is produced from specified material and is machined to close
tolerances and laid down standard of surface finish.
All the dimensions on the block are also specified and it is used to calibrate
ultrasonic flaw detectors in general. V1 blocks are used on the surface to
calibrate A-scan units and V2 blocks are used subsea by divers for calibration
checks.
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Pre-calibration checks
For portable sets check the power supply is fully charged. Switch on the set and
allow it to warm up for 15 minutes, or the manufacturer’s recommended time.
This allows the CRT and other circuits to reach operating temperature and
stabilise.
CRT display
Adjust the focus and brilliance of the spot on the CRT screen. The spot will
normally not be visible, but will, however, appear as a line across the screen.
Use the delay control to adjust the time base to display the initial pulse (the
first transmitted pulse) on the screen.
Position the course range control to the required range. (This may be between
10mm and 1m depending on the actual instrument). Select and connect the
required probe. (For thickness measurement and lamination testing, this will be
a zero degrees or normal angle compression probe – either single or twin
crystal).
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wall echoes (BWE) so that they are equally spaced along the X-axis, then adjust
the second and fourth so that they are on the fifth and tenth divisions on the
reticule. Provided this is achieved, the time base is linear.
Linearity of amplification
Set the reject or suppression control to off or zero. Place the probe over the
1.5mm diameter hole on a V1 calibration block. Adjust the gain controls to
display the height of the reflected signal to 80% full screen height (FSH).
Note: The gain settings.
Use the fine (2dB or 1dB) gain control to increase the signal by 2dB.
This represents the difference in height between 80-100% that is a ratio of 4:5,
which will increase the signal on the screen by one quarter of its displayed
height and the signal should be at full screen height.
Readjust the fine gain control to attenuate the signal back to 80% full
screen height.
Attenuate the signal by 6dB.
This represents a decrease of a half and the signal therefore should reduce to
40% of full screen height.
Now attenuate a further 12dB.
This represents a decrease of one quarter of the displayed signal and the height
should then be 10% of the full screen height.
If the gain adjustment does not produce these results the amplifier is not linear
and the instrument must be recalibrated internally, which involves stripping it
down to readjust internal trim settings.
Calibration procedure for 100mm thickness.
Place the probe onto the face of a suitable calibration or reference block that is
25mm thick ensuring there is adequate coupling.
A number of back wall echoes should be displayed on the CRT screen. Adjust
the gain settings as necessary to display the second echo signal amplitude to
75% full screen height.
Adjust the fine range and delay controls to alter the screen display so that four
back wall echoes are shown, all equally spaced across the x-axis.
As the screen on the CRT has a reticule that is divided into 10 equal segments,
the four echoes are adjusted to 2.5, 5, 7.5, and 10 divisions along the x-axis.
sensitive setting as the minimum flaw size that may be achieved is of the order
of 1 to 2λ.
Whatever the required sensitivity is should be detailed in the workbook or the
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The probe is traversed along the weld until the signal from the flaw is
maximised. Further traversing of the probe will drop the signal height on the
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CRT in the same manner as for a 6dB drop but with angle probes the signal is
reduced to one tenth using a 20dB drop. This point can be plotted and the
defect size obtained by numerous such manipulations of the probe.
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