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Report Assignment 1
GROUP 12
GROUP PERSONNEL:
ANDREAS EXA SAPUTRA (1606834522)
DANDY FADHILAH (1606890233)
KANTIA SIDIQ PERMANA (1606905361)
KIRANA WIDIANI LESTARI (1606826880)
RIEDO DEVARA YUSHARYAHYA (1606895354)
TETRA MUTIARA AFIFAH (1606828841)
Corrosion costs around 170 billion in industrial costs. The oil industry
with complex and demanding product techniques, and environmental challenges
of failing components takes the average portion of these costs. A study revealed
that corrosion of piping and pipeline in the oil and gas industry was a major
problem. Preventing corrosion is vital in every step in the production of oil and
gas (Denis, 1994).
Treatment, protection, and restoration metal has been studied and conducted
but there still has not been found the true cure for all this problem. The problem
that often occurs at this time is caused by the presence of microbes that are carried
along by the fluid, as well as the components of the fluid that are corrosive (H2S
corrosion). To overcome this corrosion, the most commonly used
countermeasures are cutting the part of the pipe that has been corroded, but the
disadvantage is that the costs will be very large. As for the use of cathodic
inhibitors but cannot optimally protect the pipe from corrosion and its use is done
continuously. Lastly, with coating but it’s difficult for the inside of the pipe.
Therefore, a survey was conducted to determine the needs of oil and gas
industry producers. A series of questions are submitted to the respondent directly
and indirectly; through online forms. From the data, we get the specifications
desired and expected by the oil and gas industry producers in this new product.
Each question is classified based on product aspects. The four main aspects
are expected to be core decisions in the final product specifications. Each need is
sorted to identify the most important customer needs and choose which ones need
to be prioritized and which ones do not. The first most important aspect is
performance protection against corrosion, including the frequency of use,
protection of metal, protecting from acid and microbes, place of use, durability,
and taking a short period of time to start acting. The second aspect is retailing, it is
expected that existing products have relatively affordable prices. The third aspect
is handling, the product is expected to be easy to use both in terms of maintenance
and post-corrosion handling. The last aspect is the expected value of the product,
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which is biodegradable, so that the finished product will not be an impurity to the
environment.
Product specifications describe the things that must be done by a product
and are intended to quantify consumer needs so that they can provide direction for
product design. Specifications consist of metrics and metric values whose values
are always followed by the appropriate unit.
After defining and quantifying the needs and specifying every aspect in
quantitative data, then benchmarking is done to clearly see the position of own
product and to find an opportunity based on quantitative data of the existing
products. To do that, benchmarking the similar products that exists in the market,
like corrosion inhibitor product (NALCO 2833, GORCARD 566, Z50-Fluid) and
coating product (Hempacore) has been done. By comparing those data, own
product finds the excitement inside of it, including the cheaper price, the cleaner
raw material, and so on.
Based on benchmarking data, anti-corrosion product ideally has the
retention time and curing time of 120-240 minutes, film persistency of 28-32
N/m2s, corrodent diffusivity of 4.8 x 10-10 m2/s, neutral acidity, room
temperature vapor pressure, good compatibility in the system, fast-acting,
biodegradable, with the price of 700-800 USD/ L.
The proposed product is targeted to piping and pipeline corrosion, this
specification are proved to be better than benchmarking data, therefore proposed
product is forecasted to satisfy the needs of market.
In conclusion, fast-acting biodegradable compound for metal treatment is
strongly suggested to become the solution of corrosion problems in piping and
pipeline.
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LIST OF FIGURES
Figure 1.1. Pie Chart of Metallic Corrosion Cost in the United States ................... 4
Figure 2.1. Schematic of How Inhibitor Film Prevents Water Contacting a Metal
Surface................................................................................................................... 12
Figure 2.2. A Typical Coating System for Marine and Industrial Applications ..... 8
Figure 2.3. Impressed Current Cathodic Protection System ................................. 12
Figure 2.4. Surface Before and After Commercial Rust Conversion Treatment .. 13
Figure 2.5. Molecular Structure of Tannic Acid ................................................... 14
Figure 2.6. Schematic of Action of Oil Field Corrosion Inhibitor ........................ 16
Figure 2.7. Coating Global Market Trend in 2016 ............................................... 19
Figure 2.8. Synthesis Procedure of Rust Converter .............................................. 22
Figure 3.1. Respondents’ Frequency..................................................................... 29
Figure 3.2. Respondents’ Common Types of Corrosion ...................................... 30
Figure 3.3. Grouping Types of Corrosion ............................................................. 30
Figure 3.4. Respondents’ Corrosion Site in Pipes ................................................ 31
Figure 3.5. Respondents’ Corrosion Protection Methods ..................................... 31
Figure 3.6. Respondents’ Choice of Corrosion Protection Product’s Notable
Aspects .................................................................................................................. 32
Figure 3.7. Respondents’ Corrosion Countermeasure .......................................... 33
Figure 3.8. Respondents’ Corrosion Restoration Method ..................................... 33
Figure 3.9. Respondents’ Choice of Corrosion Restoration Product’s Notable
Aspects .................................................................................................................. 34
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LIST OF TABLES
Table 1.1. Diagram of Metallic Corrosion Cost in the United States ..................... 4
Table 2.1. Organic Coating ................................................................................... 17
Table 2.2. Local Toxic Level in Phosphating System .......................................... 25
Table 3.1. Customer Needs Interpretation ............................................................ 35
Table 3.2. List of Customer Needs........................................................................ 38
Table 3.3. Category of Customer Needs and Needs Rank .................................... 38
Table 4.1. List of Specification Metrics ................................................................ 40
Table 4. 2 List of Metrics ...................................................................................... 43
Table 4.3. Benchmarking table ............................................................................. 49
Table 4. 4 Specifications list table ........................................................................ 55
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Figure 1.1. Pie Chart of Metallic Corrosion Cost in the United States
(Source: https://sellmyhou.se/)
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Oil and gas industry deals with high number of metals corrodent, such as
H2S and CO2. As oil and gas may contain corrodents, it is necessary to control the
composition of those acid chemicals so that the quality of metal in the piping and
pipeline can be maintained.
There are many methods available to control corrosion on metal piping
and pipeline, for example by doing routine checking in a certain period of time or
by applying metal protection compound like coatings as primary mitigation, and
cathodic protection method as the secondary mitigation.
As countermeasures of dealing with corrosion, science continues to
develop today to create new innovations in corrosion protection products, ranging
from protective coating technology as metal pre-treatment before usage, material
selection of corrosion inhibitors, remote real-time maintenance and checking, and
other efforts to reduce the corrosion rate.
1.2 Product Usage (Formulation of Problem)
In overcoming the problems that occur due to corrosion, metal treatment
routine can be done continuously. However, some treatments may possess specific
disadvantages according to the chemical used as the anti-corrosion compound. For
example, by giving a metal anti-rust coating, there are shortcomings such as anti-
rust coating base compounds are not so environmentally friendly. So that if the
anti-rust layer is in contact with the environment, it will have a negative impact on
the surrounding environment, especially when they are difficult to decompose and
considered toxic to the health of living things. Easy-peel-off coatings can also
become an issue as they have the potential to get exposed to environment and will
be contaminate the surroundings.
One effort that can be done to reduce the above problems is to do metal
treatment with materials that are environmentally friendly or often called
biodegradable. Biodegradable is one method that is being explored by research to
preserve the environment and reduce waste that is harmful to the environment due
to the biodegrable nature this is easily broken down by the environment and also
microorganisms and also does not pollute the environment so it is safe for health.
The next characteristic possessed by biodegradable is that it is easy to react when
used so it does not need to wait long until the material contained is active.
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CHAPTER 2
REVIEW OF LITERATURE
And overall
𝐶𝑂2 + 𝐻2 𝑂 + 𝐹𝑒 → 𝐹𝑒𝐶𝑂3 + 𝐻2 (2.4)
2.1.1.2 Hydrogen Sulfide
According to Oilfieldwiki Inc, Hydrogen Sulfide is another problem in oil
and gas industry. Hydrogen sulfide forms a weak acidwhen dissolved in water, it
is a source of hydrogen ions and turns corrosive. The forms of this corrosion are
uniform, pitting, and cracking.
2.1.1.3 Oxygen
Oxygen is a strong oxidant that reacts with the metal very quickly and may
acceleratethe anodic destruction of metal. The presence of oxygen magnifies the
corrosive effects of the acid gases (H2S and CO2). The forms of corrosion
associated with oxygen are mainly uniform corrosion and pitting-type corrosion
(Satyendra, 2015).
2.1.1.4 Two Metal Galvanic Action
According to Mckey and Worthington (1936), contact between two metals
that have a difference potential and exposed to the electrolyte environment will
cause the metal to corrode. In this situation, metal with a negative potential
becomes the anode and begins to rust. Anodes lose metal ions to balance the flow
of electrons, because metals are made up of crystals, many of such cells are set up,
causing intergranular corrosion. In addition, electrochemical potential differences
can also produce crevice and cause pitting corrosion. This crevice will be where
oxygen dissolves in the liquid which is stagnant and causes corrosion destruction
under the pipe.
2.1.1.5 Fluid Flow
The presence of turbulence fluid flow with solids which are carried in the
fluid can cause erosion corrosion. This corrosion is caused by damage to the
protective layer in the pipe. The protective layer is a thin film that serves to
stabilize the corrosion reaction and slow it down. This form of corrosion is
recognized as being caused by wear on the pipe walls (Lecan et al, 2013).
2.1.1.6 Biofilm
A biofilm is a complex aggregation of microorganisms growing on a solid
substrate. Biofilms are characterized by structural heterogeneity, genetic diversity,
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Othercriteria for fast acting is how effective the performance of our product is
when used in emergency.
2.4 Basic Principle of Metal Treatment Compound
2.4.1 Corrosion Inhibitor
Corrosion inhibitors are chemical compounds that are added to a fluid to
reduce the rate of corrosion in materials in contact with the fluid. For example, an
inhibitor will be injected into the stream of hydrocarbons (oil or gas) near to the
wellhead to reduce corrosion in the steel of the pipeline. The composition of the
flow from the wellhead can vary greatly, with the water content varying from
between 1 and 99%, for example, and this has a significant effect on the natural
corrosion potential in the untreated system. Other factors, such as temperature and
pressure also affect corrosion rates (Hobbs, 2014). While corrosion inhibitors are
effective against 𝐶𝑂2 𝑎𝑛𝑑 𝐻2 𝑆,if oxygen is present they are either ineffective or
require very high concentrations to achieve the desired inhibited corrosion rate
(Winning, et al, 2010). In these conditions, scavengers are used to remove the
oxygen. Also, any water injected into the well would be treated to remove oxygen
before injection.
The main mechanisms for internal corrosion of pipelines are aqueous
corrosion caused by soluble corrosive gas, such as carbon dioxide, hydrogen
sulphide, or oxygen, and corrosion influenced by microorganisms. The water can
arise from being part of the original reservoir products (formation water) or from
water injection used to increase pressure. Corrosion Inhibitor are adsorbed on the
surface of the corroding metal, creating in this way a tight protective film as
illustrated in Figure 2.1.
Figure 2.1. Schematic of How Inhibitor Film Prevents Water Contacting a Metal Surface
(Source: Hobbs, 2014)
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prepared surface. Generally, a spray gun is used to generate the required heat for
melting through combustion of gases, electric arc or plasma.
Cladding is the bonding together of dissimilar metals. It is achieved by
rolling of two sheets of metal together. The principle of cladding includes hot-roll
bonding, cold roll bonding, explosive bonding, and weld cladding. For example, a
nickel and steel sheets 21 are hot rolled to get a composite nickel-steel sheet.
Similarly, high strength aluminum alloys are clad with commercially pure
aluminum to have a good barrier to corrosion.
Vapor deposited coatings are accomplished in a high vacuum chamber.
There are mainly two types of vapor deposition: physical vapor deposition (PVD)
and chemical vapor deposition (CVD). Usually, the coating material is vaporized
by heating electrically and the vapors are allowed to deposit on the part to be
protected. The major vapor deposition method are sputtering, evaporation, ion
plating (all of which are PVD processes) and CVD. The species to be deposited is
transferred and deposited in the form of individual atoms or molecules. The most
important advantage of vapor deposited thin coating is that it is pore free and
highly dense. However, its application in corrosion protection is limited since this
method is more expensive compared to other methods.
Ion implantation and laser processing are two surface modification
methods accomplished using high-energy or particle beam. High-energy ion
beams are used to modify surfaces to combat issues related to corrosion and wear.
By ion implantation, it is possible to enhance the passivation characteristics or
create a novel material. Ion implantation commonly finds its application in
semiconductor industry. Lasers with output power 0.5 to 10 kW can be employed
to engineer the metallurgical structure of a surface and tailor its surface property
by leaving its bulk properties intact. Laser processing helps to produce corrosion
resistant surface layers. Transformation hardening, surface melting, and surface
alloying achieve laser processing
2.4.2.2 Inorganic Coatings
Nonmetallic inorganic coatings include ceramic coatings, conversion
coatings, and anodized coatings. One of the most widely used ceramic coatings is
zinc silicates. These Sol-gel based silica and titania coatings are another type of
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inorganic coatings. The inorganic particles in the sol gel coatings generally act as
a good barrier against corrosive species. But, the sol gel coatings cannot be
prepared in the thickness required for very high corrosion resistance since it is
prone to have cracks in the coating.
Next, Phosphate coating and chromate conversion coatings are two largely
used inorganic conversion coatings. Phosphate coating is produced on the metal
surface by immersion the metal in a bath mainly contains phosphoric acid and
other chemicals. During the immersion, the metal reacts with phosphoric acid and
other chemical contained in the bath and produce a crystalline insoluble protective
phosphate layer. Phosphate conversion coatings are generally used to improve the
corrosion resistance and the adhesion of paints. Commonly used phosphate
conversion coatings are zinc phosphate, iron phosphates, and manganese
phosphates. The basic principle involves in any phosphate coating is the
precipitation of a divalent metal and phosphate ions (𝑃𝑂43− ) on a metal surface.
The phosphate conversion coatings can be applied either by spraying or by
immersion.
Chromate conversion coatings are produced on the metal surface by a
chemical or electrochemical treatment of the metals or metallic coatings in
solutions containing hexavalent chromium (𝐶𝑟 6+ ) and other components.
Chromate conversion coatings are primarily applied to improve the corrosion
resistance of the metal and to improve the adhesion of paints on the metal surface.
Chromate conversion coatings are applied by both spraying and immersion
methods. However, various governments and regulatory bodies recommend the
replacement of chromate conversion coating with some other green alternative
since hexavalent chromium is carcinogenic and toxic.
Anodizing is one of the most important surface modifications carried out
for aluminum alloys for improving the corrosion resistance and other purposes.
Aluminum oxide (𝐴𝑙2 𝑂3) films are formed on the surface when aluminum and
aluminum alloys are polarized anodically in electrolyte solutions. Since all of the
anodic process form porous 𝐴𝑙2 𝑂3films, it is required to seal the pores by
immersion the coated materials in hot water. The hot water treatment would
hydrate the coating and seal the pores by forming 𝐴𝑙2 𝑂3 . 𝐻2 𝑂.
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Figure 2.2. A Typical Coating System for Marine and Industrial Applications
(Source: https://www.steelconstruction.info, .n .d)
Prior to the application of a primer, the substrates to be coated should be
cleaned neatly and pretreated to improve the adhesion of the subsequent coatings.
Generally, sand blasting, polishing with emery sheets and pickling are employed
for surface finishing. Next, the primer is the base coat on which the rest of the
coating system is applied and hence it should have strong adhesion to the surface
of the substrate. The primer generally contains some inhibitive pigments and these
pigments used to passivate the metal surface and improve its corrosion resistance.
A primer should protect the surface for many days or months prior to the
application of top coats and thus the primer coat should be highly adherent and
inert.
The next layer is intermediate coating which is to increase the thickness of
the coating system and resist the infiltration of corrosive species to the metal
surface. The major use of intermediate coats is to build up the thickness of the
coating, Improve the chemical resistance of the coating, Retard the moisture vapor
transfer, Increase the electrical resistance of the coating, Improve the adhesion
between the primer and topcoat.
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The topcoat is the final finish coat it is always exposed to the external
environment. The topcoat should have required colour and gloss to please the eyes
of an observer. It is the first line of defense against corrosion in a coating system
and hence it should have enough barrier property to impede the transport of
aggressive species through the coating system. The important function of a
topcoat is to provide A resistant seal for the coating system, Initial barrier to the
external environment, Good resistance to water, chemicals, and weather, Strong
and wear resistant surface, Aesthetic look to the coating system, High resistance
to ultraviolet radiation. The above-mentioned coating system is not necessary for
all applications.
Different combinations of coating system can be obtained depending upon
the corrosive situations. Even a single coat can function satisfactorily for some
corrosive environment. Sometimes a single coating formulation applied in more
than two coats can provide required protection for metals and alloys.
2.4.3 Cathodic protection
Cathodic protection is an electrical method of control or preventing
external corrosion of pipeline steels and other metallic structures buried in soil or
submerged in water (Bushman, 2012). The cathodic protection principle is based
on reversibility of electron flow to prevent current leaving the corroding area or
moving the equilibrium potential of the structure to be protected to a more
electron negative value (lower potential) and supply external source of current to
flow into the structure (Talbot, 1998). The principle of cathodic protection can be
explained with electrochemical reactions. In corrosion of iron, the metal ion enters
solution at the anodic areas in a quantity equals to cathodic reactions and flow to
the cathodic areas so that electrons on both sides are balanced.
At the anodic areas, atoms of metal release electron to become metal ions
as shown below
2𝑀 → 2𝑀+ + 2𝑒 − (2.5)
M is the metal atom, 𝑀+ is the metal ion and 𝑒 − is electron.
A general reaction at the anode where iron is corroding in non-acidic
environment such as water or soil electrolyte is represented as:
𝐹 → 𝐹 2+ + 2𝑒 − (2.6)
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The reaction released free electron that remains in the structure of the
metal and the metal ions move away from the metal structure and enter the
environment where it is consumed at the cathodic area.
At cathodic area in acidic solution in the presence of water, the reaction is
represented as:
2𝐻 + + 2𝑒 − → 𝐻2 (2.7)
The reaction produced two hydrogen ions to form two atoms of hydrogen.
Another possible cathodic reaction in aerated water or soil that is non-acidic
where oxygen is dissolved in a solution and consumed but still corrosion occur at
the anode and not at the cathodic is represented as:
𝑂2 + 2𝐻2 𝑂+4𝑒 − → 4𝑂𝐻 − (2.8)
The whole of equations (2) to (4) which are electrochemical reactions that
occur during corrosion process can be summarized into one equation as shown:
2𝐹𝑒 + 2𝐻2 𝑂 + 𝑂2 → 2𝐹𝑒(𝑂𝐻)2 (2.9)
There are basically two techniques of applying cathodic protection to
protect structures, namely sacrificial anode and impressed current techniques.
2.4.3.1 Sacrifial Anode
Sacrificial anode system involves connection of a more negative
electrochemical metallic anode with the intended structure to be protected via a
wire to complete the circuit. The method of protection requires no external power
source but based on the natural potential existing between sacrificial anode and
protected structure. For sacrificial anode system, the metallic anode dissolves, get
consumed gradually and the current flow from the anode through the soil
(electrolyte) down to the protected structure because of natural potential
difference between the protected structure and the metallic anode (Ameh, et al,
2017).
Metallic anodes commonly used in the protection of steel structures are
magnesium, zinc and aluminum and their selection depend largely on electrolyte
conductivity or resistivity. Thus, magnesium is most suitable in seawater;
aluminum in freshwater but zinc can be used in both seawater and land. It is less
expensive to install, lower maintenance cost and the current distribution to the
intended structure is quite uniform and therefore pose no risk of overprotection
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and potential coating damage. However, the current output delivery is small
compared to impressed current system, so it is only effective for smaller structure.
One other obvious disadvantage of the protection system is that the sacrificial
anode gradually gets consumed, thus needing replacement after depletion (Ameh,
et al, 2017).
2.4.3.2 Impressed Current
Impressed current cathodic protection system uses highly energized (inert)
anodes such as silicon cast iron, graphite, platinum clad, silicon mixed metal
oxide, and niobium coated wire which are then connected to positive terminal of
the power source (rectifier) and to the anode while structure intended to be
protected is connected to the power source negative terminal. The original power
source which is alternative current is converted to direct current by a rectifier
(Bushman,2012). The inert anode for the impressed current system remained
undissolved and non-consumed throughout the protection period but in the
process the inert anode causes hydrogen gas evolution reaction at the anodic
region. For structures’ potential to be lowered or cathodically protected, the
structures must be in contact with power source and in electrolytic environment.
The impressed current cathodic protection system delivers adequate
power output and therefore used for protection of larger structures and several
kilometers of pipelines. Above all, the inert anodes are not consumed, hence
requires no replacement. But the current distribution is usually not uniform
leading to overprotection and coating damages of structures that are in closed
proximity to the power source if not insulated. It has become necessary to
critically evaluate design processes of cathodic protection system due to rising
corrosion and increasing pipelines construction and installation in very harsh
environment owing to remote oil and gas exploitation and exploration (Ameh, et
al, 2017).
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Figure 2.4. Surface Before and After Commercial Rust Conversion Treatment
(Source: Viswanathan, 2019)
Rust converter reduces the corrosion rate of rusted metals either when used
alone or in combination with a primer . In practical applications, an initial rust
converting coating will be followed by a topcoat. For performance improvement,
additives such as active agent, catalytic agent, corrosion inhibitor, penetrating
agent and wetting agent, are added in commercial rust converting paint
formulation (Marco et al, 1994).
2.4.5.1 Tannins-Based
Tannin and its derivatives are the major group of chemicals investigated
for rust converter applications. On reaction with iron oxides, tannin-based
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compounds can form iron tannates that appear as a blue/ black protective layer on
the surface. The performance of these compounds depends on several parameters
such as the type of tannin used, concentration, pH, time of exposure, reaction
time, nature of co-additives, application method, the extent of corrosion happened,
electrolyte aggressiveness and contamination grades of the rusted steel.
(Viswanathan S.Saji, 2019)
Tannins (hydrolysable and condensed tannins) are high molecular weight
polyphenolic compounds. Tannic acid, the most widely investigated tannin (Fig.
2.5) is a hydrolysable tannin (ß-1,2,3,4,6-digalloyl-O-D-glucose) with
approximate empirical formula 𝐶76 𝐻52 𝑂46. Due to the presence of ortho −OH
groups on the aromatic rings, tannic acid can chelate with metal ions forming a
highly crosslinked network of ferric tannates.
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even higher) a partially hydrolyzed ferric tannate complex and some 𝐹𝑒 2+ in the
form of hydrated polymeric ferrous tannate are obtained. These phases do not
provide corrosion protection (Jaen et al, 2011)
2.4.5.2 Phosphoric Acid-Based
Leonard said, 𝐻3 𝑃𝑂4 insufficient amount can act as a rust remover,
converter, and inhibitor in paint compositions. The use of 𝐻3 𝑃𝑂4in rust converter
formulations is based on its ability to form water-insoluble iron phosphate
(𝐹𝑒3 (𝑃𝑂4 )2 ) on steel surface. A waterborne epoxy ester resin rust converting
primer containing TiO2, bentonite, and 𝐻3 𝑃𝑂4 showed good physical and
corrosion-resistant properties.
Almeida et al. explained the mechanism of phosphoric acid pretreatment
for rusted surfaces. On reaction with rust, phosphoric acid can give amorphous or
crystalline iron phosphates and that depends strongly on the concentration of the
phosphoric acid solution. For a surface that corroded for 10 months in an
atmosphere with low level of contamination, phosphoric acid solutions of ca.
7.5wt.% not converted residual rust eficiently whereas at a higher concertation
(14.6%), formation of a less adherent bluish-white film was formed corresponding
to the formation of vivianite [𝐹𝑒3 (𝑃𝑂4 )2.8𝐻2 𝑂]. At concentration > 33.2%, a
vitreous dark brown film was formed which exhibited more and more cracks,
discontinuities and higher acidity as the concentration increased.
Phosphoric acid can react with different components of rust and can give
rise to various iron phosphates [𝐹𝑒(𝐻2 𝑃𝑂4 )2 , 𝐹𝑒(𝐻2 𝑃𝑂4 )2 and𝐹𝑒3 (𝐻2 𝑃𝑂4 )8].
The dihydric phosphates formed can be converted into indissoluble phosphates
(FeHPO4, 𝐹𝑒3 (𝑃𝑂4 )2, and FPO4 ) with time (Burtnieks, 1975)
2.5 Product Trends
2.5.1. Corrosion Inhibitor
Typical corrosion inhibitors used in oil and gas industries revolve around
organic compounds and are employed in small concentrations (less than 0.1 %).
Often categorized as mixed inhibitors, they adsorb on steel surfaces and inhibit
anodic and cathodic reactions. It also displaces adsorbed water molecules from the
surface and are referred as filming inhibitors. (Palmer, Hedges and Dawson,
2004).
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Almost all organic inhibitors are highly polar functional compounds, with
many being based on nitrogen, such as amines, amides, imidazolines or
quaternary ammonium salts, and include salts of nitrogenous molecules with
carboxylic acids, poly-oxyalkylated nitrogen containing compounds, nitrogen
heterocyclics and compounds containing P, S, and O (Palmer, Hedges and
Dawson, 2004).
Furthermore, the molecules also have a hydrocarbon chain attached, at
which the length varies (carbon numbers between 12 and 18). The active group
provides the ability to displace water and cause adsorption onto the metal surface.
The hydrocarbon causes the molecule to be partially oil soluble and attracts crude
oil molecules from the process stream. The inhibitor molecule protects metal the
surface by providing a barrier from the corrosive water phase. (Palmer, Hedges
and Dawson, 2004).
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100
80
60
40
20
0
North America South America Middle East Europe North Africa Asia
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Mineral acids such hydrochloric acids, sulphuric acid, and phosphoric acid
are usually used for surface finishing process. Exposure usually is accidental and
often is due to inadequate use of protective measures. Acid burns are a unique
clinical entity. Dilute solutions deeply penetrate before dissociating, thus causing
delayed injury and symptoms.
Organic acid such as tannic acid is another type of corrosion inhibitor,
however tannic acid and water expectably reduces the pH level below 7, leading
to a far more acidic environment which has adverse consequences. The shift in the
pH is often too sudden to sustain a constant population.
Another example of chemical rust removing agent is hydroxyethane
diphosphonic acid (HEDPA). According to Rao et al (2012), chemical processing
of HEDPA (>5vol.%) at high temperature (> 40oC-55oC) produces strong pungent
smell and unpleasant cleaning environment. In contrast of what usually chemical
contributes to living beings’ mortality, low concentration (<0.5wt.%) of HEDPA
improved seeds germination and plants growth. However high concentration of
HEDPA produces reverse effect.
2.6.4 Coating Pigments
Pigments are inorganic or organic compounds that provide colors to the
coating. Color and visible opacity is necessary to observe coating flow and
durability. However, pigments often contain heavy metals such as cadmium, lead,
zinc, chromium and cobalt. According to Porwal (2015), The World Health
Organization (WHO) has reported a 20%-40% increased risk of certain types of
cancer for those who come into regular contact with, or work with paint.
2.6.5 Phosphate Coatings
There are several operations to be done as surface preparation to give
protective coatings to the metal. The most common one is phosphate coating
which promotes adhesion of organic coating onto metal surface and retard
corrosion. The process consists of a series of chemicals and rinse baths and most
of the hazardous waste produced in a metal finishing facility comes from waste
water generated by the rinsing operations that follow cleaning and plating.
The mechanism of phosphate of processing is to coat metal with phosphate
containing mixture of hopeite and phosphophyllite layer after immersion in a
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The waste outlet contains wastewater from processing steps, solid rust
residue from steel sheet during pre-degreasing operation, sludge precipitate from
phosphating, and slime from neutralization process for wastewater treatment.
According to Weng (1998), Total calculated of wastewater may numbered up to
20,800 𝑔/𝑚2 and solid residue up to 49.0 𝑔/𝑚2 . Unlike the wastewater
discharge, solid residue cannot be absorbed by the environment. A single-factor
analysis of LTL (Local Toxic Level) is conducted from wastewater, and the
results are listed in Table 2.2. The average LTL value is 1.6 ppm/ppm, which
demonstrates wastewater must be treated before disposal.
Table 2.2. Local Toxic Level in Phosphating System
Substance 𝐹 𝑃𝑂43− 𝑆𝑂42+ 𝑍𝑛2+ 𝑀𝑛2+ 𝑁𝑖 2+ Oil Suspended Average
Solids
LTL 1.3 2.9 1.5 2.1 1.3 1.4 1.1 1.3 1.6
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CHAPTER 3
MARKET NEEDS ANALYSIS
interviews. We also obtain additional literature from the interviews with some
experts and professionals that interacts with piping and pipelines in oil and gas
field. Those customer voices are affecting the sustainability of product design and
development.
To understand what customer needs, first we ought to define our customer
specifically. The customers include both those who will buy the product and those
who will use the product. Therefore, we gather information from, industry
professionals as user of the product and experts related to this field. Here are the
results of the survey.
3.1.2.1. Usage Frequency of Anti-Corrosion Protection
Continues (remote)
monitoring
(Tentative) Depends on
22%
the case
34%
Once in a month
11%
Twice in a month
11%
22%
3 bulan sekali
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Stress Corrosion
Cracking
Localised Corrosion
12%
25%
6%
Crevice Corrosion
6%
CO2 Corrosion
25%
37% general corrosion
acidic corrosion
microbial corrosion
38%
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Internal flowline
41% 41%
Pipe Support
external flowline
18%
Brushing
27%
40% Sprinkle
Painting
Spraying
13%
injection
13% 7%
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Fast-Acting
21% Durable
28%
3% Heat Resistant
7% Non-Volatile
No Smell
17% 24%
Economic
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rust converter
22%
rust remover
17%
brushing
spraying
25% 58%
roll on
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9%
Fast-acting
18%
46% Durable
Odorless
Non-volatile
27%
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Table 3.1. Customer Needs Interpretation (Continued.)
No. Questions Answers Needs
As Cutting off part of the
countermeasure(s) pipe
of corrosion on Blasting
Anti-Corrosion Treatment
pipe, which
that uses mechanical handling
9 method(s) listed
as post corrosion
below are usually
Coating countermeasure
used?
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CHAPTER 4
PRODUCT SPECIFICATIONS
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Table 4. 2 List of Metrics
Metrics
Com-
Film Diffu Con- pound Wet-
Tough- Pre- Reacti- Heat Hydrolytic Degradation
No List of Needs Time Persis- sivi- centra- res- tabi- Price
ness ssure vity Resistance activity rate
tency ty tion pond lity
time
mi Charge
days years N/m2.s m2/s mol/L [M]/s N/m J/m3 Pa keff o
C/Watt USD %
n (electron)
Product Performance / Functionality
Anti-Corrosion
Treatment
1 • •
Compound that can
be used continuously
Anti-Corrosion
Treatment
Compound that can
2 •
protect metals from
various types of
corrosion
Anti-Corrosion
Treatment
Compound that can
3 •
protect metals from
corrosion in acidic
environment
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Table 4.2. List of Metrics (Continued.)
Metrics
Com-
Con-
Film pound Wet-
Diffus cen- Tough- Pre- Reacti- Heat Hydrolytic Degradation
No List of Needs Time Persis- res- tabi- Price
-sivity tra- ness ssure vity Resistance activity rate
tency pond lity
tion
time
mol/ Charge
min days years N/m2.s m2/s [M]/s N/m J/m3 Pa keff o
C/Watt USD %
L (electron)
Anti-Corrosion
Treatment
Compound that
4 can protect metals •
from corrosion in
microbial
environment
Anti-Corrosion
Treatment
Compound that
5 can be applied on •
any part of the
pipeline and/or
piping
Anti-Corrosion
6 Treatment that is • • • •
durable
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Table 4.2. List of Metrics (Continued.)
Metrics
Com-
Con-
Film pound Wet-
Diffus cen- Tough- Pre- Reacti- Heat Hydrolytic Degradation
No List of Needs Time Persis- res- tabi- Price
ivi-ty tra- ness ssure vity Resistance activity rate
tency pond lity
tion
time
mol/ Charge
min days years N/m2.s m2/s [M]/s N/m J/m3 Pa keff o
C/Watt USD %
L (electron)
Anti-Corrosion
Protection
Compound that is
7 compatible with •
the fluids carried
by the pipeline
and/or piping
Anti-Corrosion
Protection
8 •
Compound that
resists heat
Anti-Corrosion
Treatment
Compound that
9 •
takes a short
period of time to
start acting
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Table 4.2. List of Metrics (Continued.)
Metrics
Com-
Con-
Film pound Wet-
Diffus cen- Tough- Pre- Reacti- Heat Hydrolytic Degradation
No List of Needs Time Persis- res- tabi- Price
ivi-ty tra- ness ssure vity Resistance activity rate
tency pond lity
tion
time
mol/ Charge
min days years N/m2.s m2/s [M]/s N/m J/m3 Pa keff o
C/Watt USD %
L (electron)
Retailing
Anti-Corrosion
Treatment
10 Compound that •
has a relatively
affordable price
Added Value
Anti-Corrosion
Treatment
11 • •
Compound that is
biodegradable
Handling
Anti-Corrosion
12 Protection Method •
that is simple to do
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Table 4.2. List of Metrics (Continued.)
Metrics
Com-
Con-
Film pound Wet-
Diffus cen- Tough- Pre- Reacti- Heat Hydrolytic Degradation
No List of Needs Time Persis- res- tabi- Price
ivi-ty tra- ness ssure vity Resistance activity rate
tency pond lity
tion
time
mol/ Charge
min days years N/m2.s m2/s [M]/s N/m J/m3 Pa keff o
C/Watt USD mol/g.day
L (electron)
Anti-Corrosion
Treatment that
uses mechanical
13 •
handling as post-
corrosion
countermeasure
(Source: Private Data, 2019)
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Scores
Needs Metric Needs Competitor
No. Needs Description Specification Own
Group Unit Rank NALCO CORGARD Z50- Hempacor
Product
2833 566 Fluid e
Anti-Corrosion
Performa
Product
Retention time
Treatment Compound
nce
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fluid
Scores
Needs Metric Needs Competitor
No. Needs Description Specification Own
Group Unit Rank NALCO CORGARD Z50- Hempacor
Product
2833 566 Fluid e
pH level of the
Product Performance
anti-corrosion
Anti-Corrosion treatment
[H+]
(continued)
Treatment compound
Compound that can Local oxygen (mol/L) 10-14-10- 10-10-
3 5 10-7 12,5 10-8-10-6 10-9-10-6
protect metals from concentration on 10-9
corrosion in acidic the protection mol/L
environment film of anti-
corrosion
compound
Anti-Corrosion
Treatment Corrodent
Compound that can diffusivity from
4 protect metals from the fluid to the m2/s 5 2.10-10 N/a N/a N/a N/a
corrosion in metal (on the
microbial protection film)
environment
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Scores
Needs Needs Metric Needs Competitors
No. Specification Own
Group Description Unit Rank NALCO CORGARD Z50-
Product Hempacore
2833 566 Fluid
Anti-Corrosion
Performance
Treatment
(continued)
Wettability
Product
Compound that
of corrosion 5
5 can be applied N/m ••• •• • ••• ••
prevention
on any part of
compound
the pipeline
and/or piping
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Scores
Needs Needs Metric Needs Competitors
No. Specification Own
Group Description Unit Rank NALCO CORGARD Z50-
product Hempacore
2833 566 Fluid
Product
Anti- Toughness of
Performan
Corrosion anti-
ce 6 J/m3 5 ••• ••• •• •• ••
Treatment that corrosion
(continued
is durable agent
)
Vapor
pressure of
anti- 3.10-4 at 1,3.10-4 4,84.10-3 at
MmHg N/a N/a
corrosion 27oC at 21oC 25,3oC
protection
compound
Life time of
anti-
years 3 - - - 3
corrosion
coating-type
Life time of
anti- minutes 240 180 210-220 130 -
corrosion
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(corrosion
inhibitor)
Scores
Needs
Needs Needs Metric Competitor
No. Specification Own
Group Description Unit Rank NALCO CORGARD Z50-
Product Hempacore
2833 566 Fluid
Anti-Corrosion
Protection
Performance
(continued)
Compound that
Product
is compatible Reactivity 5
7 keff <1 N/a N/a 0,8 -
with the fluids with fluids
carried by the
pipeline and/or
piping
Thermal
Anti-Corrosion resistance of
Protection anti- o 4 0,085-
8 C/Watt 0,09 0,042 0,067 N/a
Compound that corrosion 0,091
resists heat protective
compound
Anti-Corrosion Anti- 5 2 for CI
9 minutes 5-6 2 3-5 180
Treatment corrosion 60 for
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Need Scores
Needs Specificat Metric Competitors
No. Needs Description s Own
Group ion Unit NALCO CORGA
Rank Product Z50- Fluid Hempacore
2833 RD 566
Anti-Corrosion
Retailin
value
Hydrolytic Charge
11 Treatment Compound 2 • - - N/a -
d
activity (electron)
that is biodegradable
Degradati
on rate in
% • - - • •
microbial
digestion
3-8 for CI Continuous
Handlin
Anti-Corrosion
Applicatio 120 (per when
12 Protection Method Minutes 5 3-12 8-15 120 (per km)
g
anti-corrosion
treatment
Anti-Corrosion [H+]
(continued)
compound
Treatment Compound
Local oxygen (mol/L)
3 that can protect metals 5 10-7 10-14-10-12,5 10-7
concentration on
from corrosion in acidic mol/L
the protection
environment
film of anti-
corrosion
compound
Anti-Corrosion Corrodent
Treatment Compound diffusivity from
m2/s 1.10-10-5.10-
4 that can protect metals the fluid to the 5 2.10-10 N/a 10
from corrosion in metal (on the
microbial environment protection film)
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Anti-Corrosion
Wettability of
Treatment Compound
corrosion 5
5 that can be applied on N/m ••• •-••• •••
prevention
any part of the pipeline
compound
and/or piping
Toughness of anti-
uct
6 Treatment that is 5
corrosion agent
durable
Vapor pressure of anti- >10-3 at >10-4 at
3.10-4 at
corrosion protection MmHg room room
27oC
compound temperature temperature
Life time of anti-
years 3 1-2 3-5
corrosion coating-type
Life time of anti-
corrosion (corrosion minutes 240 30-120 120-240
inhibitor)
Anti-Corrosion
Protection Compound 5
7 Reactivity with fluids keff <1 0,7-0,8 0,8<x<1
that is compatible with
the fluids carried by the
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Anti-
Anti-Corrosion
Performance
Anti-Corrosion
Retailing
•• •
de
ue
11 2 0-••
d
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CHAPTER 5
CONCLUSION
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REFERENCES
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http://www.environment911.org/Environmental_Issues_With_Galvanizing
[Accessed 18 Feb. 2019].
Hobbs. (2014) Reliable Corrosion Inhibition In the Oil and Gas Industry.
[Online] Available at: http://www.hse.gov.uk/research/rrpdf/rr1023.pdf
[Accessed 17 Feb 2019]
Impressed Current Cathodic Protection System for Corrosion Prevention in
Buried Pipelines of Balochistan, Pakistan. IOP Conference Series: Materials
Science and Engineering, IOP Publishing.
ISPAT. (2015). Oxygen and Steels .[Online] available at:
https://ispatguru.com/oxygen-and-steels/ [Accessed on 17 February 2019]
J.A. Jaén, J. De Obaldía, M.V. Rodríguez.(2011) Application of Mössbauer
Spectroscopy to the Study of Tannins Inhibition of Iron and Steel Corrosion.
[Online] Available at: https://doi.org/10.1016/j.porgcoat.2018.11.013
[Accessed on 17 February 2019]
J.F. Marco, J. Dávalos, M. Gracia, J.R. Gancedo, (1994). Corrosion Studies of
Iron and Its Alloys Of 57Fe Mössbauer Spectroscopy. [Online] Available at:
https://link.springer.com/article/10.1007%2FBF02074263 [Accessed on 17
February 2019]
J. S. Mandke. (1990). Corrosion Causes Most Pipeline Failures In Gulf Of
Mexico. [Online] available at:https://www.ogj.com/articles/print/volume-
88/issue-44/in-this-issue/pipeline/corrosion-causes-most-pipeline-failures-
in-gulf-of-mexico.html [Accessed on 18 February 2019]
Joanna Brzeszcz, Anna Turkiewicz.(2015). Corrosion Inhibitors Application in
Oil Industry. [Online] available at: [Accessed on 17 February 2019]
Jom. (2013). Corrosion in the Oil and Gas Industry: An Increasing Challenge for
Materials [Online] Available at:
https://link.springer.com/article/10:1007/s11837-013-0675-3 [Accessed on
17 February 2019]
Khan, M. S., et al. (2018). Efficiency and Cost Analysis of Power Sources .
Lecan et al. (2013). Corrosion Problems During Oil and Gas Production and Its
Mitigation.
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APPENDICES
APPENDIX A.
SURVEY QUESTIONNAIRE
1. Informasi Responden
a. Nama Lengkap :
________________________________________
b. Pekerjaan :
________________________________________
c. Region Operasional Perusahaan : Onshore / Offshore
d. Apakah pekerjaan anda berhubungan dengan piping di
industri atau transportasi pipeline?
a) Berhubungan langsung.
b) Tidak berhubungan.
c) Tidak berhubungan langsung, namun memiliki
pengetahuan tentang proteksi dan restorasi bahan
logam.
2. Current Problems
3. Pencegahan Korosi
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4. Penanggulangan Korosi
Penanggulangan korosi di sini dimaksudkan sebagai upaya restorari
dari logam pada piping maupun pipeline yang sudah berkarat.
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