Relevant bibliographies by topics / Corrosion resistant materials

Academic literature on the topic 'Corrosion resistant materials'

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Published: 4 June 2021
Last updated: 30 July 2024

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Journal articles on the topic "Corrosion resistant materials"

1

Bond, S. H. "‘Corrosion resistant materials handbook’." British Corrosion Journal 21, no. 3 (January 1986): 148–50. http://dx.doi.org/10.1179/000705986798272145.

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Walker, P. A. "Corrosion resistant materials handbook." Materials & Design 8, no. 2 (March 1987): 129. http://dx.doi.org/10.1016/0261-3069(87)90126-9.

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3

Ndukwe, Agha Inya, Chukwuma Daniel Okolo, and Benjamin Uchenna Nwadirichi. "Overview of corrosion behaviour of ceramic materials in molten salt environments." Zastita Materijala 65, no. 2 (June 15, 2024): 202–12. http://dx.doi.org/10.62638/zasmat1128.

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This study reviewed previous studies between the years 2015 and 2021 on how ceramic materials degraded in the presence of molten salt environments. The processes of corrosion resistance of various ceramic compositions subjected to various molten salt compositions and temperatures were also scrutinized. The results offer important new insights into the variables affecting ceramics' corrosion behaviour and the production of corrosion products. The reported result reveals that the ceramic material with the composition (Sm0.5Sc0.5)2Zr2O7 performed better than that of Sm2Zr2O7 in terms of hot corrosion resistance in molten salt (V2O5 + Na2SO4). It has also been reported that corrosion behaviour is influenced by particle size. Notably, zirconia (n-YSZ) with nanoscale grain sizes was more susceptible to hot corrosion, which was explained by increased specific surface areas. On the other hand, sintering and additives have been found to enhance corrosion resistance. The Y-Y2Si2O7 ceramic's resistance to corrosion in (V2O5 + Na2SO4) molten salt was enhanced by the addition of alumina. The results of these investigations help us understand how corrosion works and what influences ceramic materials' susceptibility to deterioration in molten salt media. This information can direct the creation of more corrosive-resistant ceramic materials for use in high-temperature environments or molten salt-based energy systems, among other corrosive uses.
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Muradyan, Sarkis, M. V. Kostina, V. S. Kostina, Ludmila Rigina, and Viktor M. Timokhin. "Cast High-Strength Wear- and Corrosion-Resistant Austenitic Nitrogen Steel for Fittings Used in Shipbuilding." Key Engineering Materials 909 (February 4, 2022): 41–47. http://dx.doi.org/10.4028/p-iqrjh9.

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The paper presents the results of studies of a new cast high-strength austenitic corrosion-resistant steel, which can be successfully used in shipbuilding for the manufacture of fittings. The authors included data on the structural-phase state of steel, the results of evaluating the mechanical properties, wear and corrosion resistance of the metal of castings in the cast and heat-treated state. The mechanical properties of steel are considered in detail in a wide temperature range. The impact strength was considered at low temperatures and static strength at 20 to 350 ° C. It is shown that steel has higher mechanical and corrosive properties in a wide temperature range than those of traditional stainless steels. The corrosion resistance of steel is considered. This is intergranular and pitting corrosion; the main types of corrosion are peculiar for shipbuilding. It has been shown that cast steel is superior to traditional corrosion-resistant steels in pitting corrosion resistance estimated by the pitting coefficient PREN and the critical temperature of pitting. The new cast steel has the same wear resistance as Hadfield steel.
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Jacobson, Nathan D., and Jude Iroh. "Shape Memory Corrosion-Resistant Polymeric Materials." International Journal of Polymer Science 2021 (June 29, 2021): 1–18. http://dx.doi.org/10.1155/2021/5558457.

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Shape memory alloys, materials capable of being deformed and maintaining the deformation and additionally capable of returning to the initial position, are valued for a range of applications from actuators to flexible microdevices. Maintaining the properties that make them useful, their ability to deform and reform, requires that shape memory alloys must be protected against corrosion, in which the integration of shape memory polymers can act as a means of protection. Thus, this review is to highlight the utility of self-healing shape memory polymers as a means of corrosion inhibition. Therefore, this review discusses the benefits of utilizing self-healing shape memory polymers for the protection of shape memory, several types of self-healing polymers that could be used, means of improving or tailoring the polymers towards specific usages, and future prospects in designing a shape memory polymer for use in corrosion inhibition.
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6

Hihara, Lloyd H. "Advanced materials for corrosion resistant coatings." Corrosion Reviews 36, no. 2 (April 25, 2018): 115–16. http://dx.doi.org/10.1515/corrrev-2018-0005.

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Nurkulov, Fayzulla, Umida Ziyamukhamedova, Erkin Rakhmatov, and Jasur Nafasov. "Slowing down the corrosion of metal structures using polymeric materials." E3S Web of Conferences 264 (2021): 02055. http://dx.doi.org/10.1051/e3sconf/202126402055.

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This article examines the resistance of corrosion-resistant polymeric materials to chemical reagents and the degree of corrosion, taking into account the direction of corrosion processes. One of the main factors that determined the corrosion rate is air humidity and dust released into the atmosphere during industrial emissions. Mixtures based on polymer materials can be used to gum up chemical apparatus and equipment; for corrosion protection, expensive materials are required. The sample is conditioned for 30 months at (23 ± 2) 0С, relative humidity (50 ± 5) %, and the thickness of the sample is determined. Resistance to chemical reagents the change in mass of samples of polymeric materials at a temperature of 35 0C for 3 months was analyzed. It was also found that by determining the corrosion rate (grade St3) by storing steel plates in a different exposure environment for 50 days. As a result, the corrosion rate of steel anti-corrosion coatings is lower than the control sample. According to the data obtained, it was found that the chloro-sulfonated polyethylene compositions are resistant to various organic solvents, acids, alkalis, oxidizing agents, and others.
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Lee, Byoung Ho, Min Ho Jo, and Yun Ha Yoo. "The Effect of Flue Gas Environment on the Corrosion Behavior of the Sulfuric Acid Dew-Point Corrosion Resistant Steel." Materials Science Forum 941 (December 2018): 1705–9. http://dx.doi.org/10.4028/www.scientific.net/msf.941.1705.

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In order to compare the corrosion resistance of conventional low carbon steel, Cu containing low carbon steel for sulfuric acid dew-point corrosion inhibition, and stainless 409L, immersion tests were carried out in 50 wt.% sulfuric acid. The effects of HCl concentraion on the corrosion behavior in a fixed sulfuric acid concentration (16.9 vol.%) was also investigated by immersion test. In addition to immersion test, field test in a thermal plant was carried out for 10 months. As a result, it was confirmed that Cu-containing dew-point corrosion resistent steel has the highest corrosion resistance compared with other materials. To verify superior corrosion resistence of dew-point corrosion resistant steel, surface morpology after various test was observed by SEM. It was found that surface corroded product of the dew-point corrosion resistant steel was much denser and thicker compared with the other steel.
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9

Umraliev, Baurzhan T., Farit A. Agzamov, Malik Z. Taskinbaev, and Aydyngali K. Seitov. "Obtaining lightweighted cementing materials from local raw materials for cementing wells in corrosion-active environment." Kazakhstan journal for oil & gas industry 2, no. 1 (March 15, 2020): 70–82. http://dx.doi.org/10.54859/kjogi95610.

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The study is devoted to the analysis of the current conditions for cementing of deepwells in Western Kazakhstan and the development of the theoretical foundations for obtaining lightweight corrosion-resistant cementing materials using local raw materials. This paper presents the theoretical justification for reducing the density of grouting materials and increasing the corrosion resistance of the resulting grouting mortars and stone with the addition of natural carbonate materials for the presence of acidic aggressive components (hydrogen sulfide and carbon dioxide) in the formation fluids. To obtain a homogeneous dense structure of cement stone, disintegration technology is justified. During the research, both standard and special methods were used to study the properties of grouting materials in a corrosive environment. Processing of experimental data and planning of the experiment was carried out using methods of mathematical statistics.
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Qiu, Ming Min, Hao Wang, Xu Wu, Hong Qun Tang, and Guang Cai Su. "Study on the Corrosion Resistance of High Boron Iron-Based Alloy." Applied Mechanics and Materials 268-270 (December 2012): 326–29. http://dx.doi.org/10.4028/www.scientific.net/amm.268-270.326.

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Being compared with traditional wear resistant materials, the corrosion resistance of high boron iron-based alloy at 25°Cand at 60°Care researched respectively. The results show that the corrosion resistance of wear-resistant alloys decline at high temperature. At 25°C and at 60°C, though the corrosion resistance of high chromium cast iron is a little higher than that of high boron iron-based alloy in acid medium (PH=3), high boron iron-based alloy’s corrosion resistance is the best among these three materials in neutral medium (PH=7) and in alkaline medium (PH=12).
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Dissertations / Theses on the topic "Corrosion resistant materials"

1

Freeman, Richard. "Corrosion & wear resistant materials for ballscrew actuator components." Thesis, University of Wolverhampton, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307165.

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Conrad, Heidi Ann. "Electrochemically Deposited Metal Alloy-silicate Nanocomposite Corrosion Resistant Materials." Thesis, University of North Texas, 2013. https://digital.library.unt.edu/ark:/67531/metadc271794/.

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Zinc-nickel ?-phase silicate and copper-nickel silicate corrosion resistant coatings have been prepared via electrochemical methods to improve currently available corrosion resistant materials in the oil and gas industry. A layered silicate, montmorillonite, has been incorporated into the coatings for increased corrosion protection. For the zinc nickel silicate coatings, optimal plating conditions were determined to be a working pH range of 9.3 -9.5 with a borate based electrolyte solution, resulting in more uniform deposits and better corrosion protection of the basis metal as compared to acidic conditions. Quality, strongly adhering deposits were obtained quickly with strong, even overall coverage of the metal substrate. The corrosion current of the zinc-nickel-silicate coating is Icorr = 3.33E-6 for a borate based bath as compared to a zinc-nickel bath without silicate incorporation (Icorr = 3.52E-5). Step potential and direct potential methods were examined, showing a morphological advantage to step potential deposition. The effect of borate addition was examined in relation to zinc, nickel and zinc-nickel alloy deposition. Borate was found to affect the onset of hydrogen evolution and was examined for absorption onto the electrode surface. For copper-nickel silicate coatings, optimal conditions were determined to be a citrate based electrolytic bath, with pH = 6. The solutions were stable over time and strong adhering, compact particle deposits were obtained. The corrosion current of the copper-nickel-silicate coatings is Icorr = 3.86E-6 (copper-nickel coatings without silicate, Icorr = 1.78E-4). The large decrease in the corrosion current as the silicate is incorporated into the coating demonstrates the increase in corrosion resistance of the coatings with the incorporation of silicates.
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Bakare, Mayowa Sunday. "The effects of microstructural modifications on corrosion resistance of metallic corrosion resistant materials Inconel 625 and FeCrMoCB." Thesis, University of Nottingham, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.546474.

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Battu, Laurent P. "Corrosion resistance of modified [beta]-Eucryptite /." This resource online, 1991. http://scholar.lib.vt.edu/theses/available/etd-08142009-040239/.

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Battu, Laurent P. "Corrosion resistance of modified β-Eucryptite." Thesis, Virginia Tech, 1991. http://hdl.handle.net/10919/44206.

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The corrosion resistance of chemically modified β-eucryptite (Li0.41Mg0.035AlP0.52Si0.480₄) having low expansion anisotropy and a near zero coefficient of thennal expansion was evaluated. Samples were exposed to aqueous hydrochloride acid at temperatures up to 100°C and environments containing sodium sulfate up to l000°C. The corrosion resistance was characterized by dilatometry, scanning electron microscopy, X-ray diffraction, energy dispersive x-ray analysis, weight variations, and mechanical properties variations. The results show that modified β-eucryptite is more severely corroded than commercial lithium-alumina-silicate glass-ceramics when exposed to these environments. Aqueous HCI removes AIP04 from modified β-eucryptite leaving a very porous structure. Molten salt corrodes modified β-eucryptite by penetration of sodium and sulfur which form an alkali melt under the surface. The modulus of rupture and the Young's modulus are reduced by both types of corrosion.
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Leavitt, Leah A. "Biodegradable packaging for corrosion inhibition via supercriticial fluid." Diss., Columbia, Mo. : University of Missouri-Columbia, 2007. http://hdl.handle.net/10355/6013.

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Thesis (Ph. D.)--University of Missouri-Columbia, 2007.
The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file (viewed on December 28, 2007) Includes bibliographical references.
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Armani, Alessandro. "Development of corrosion resistant coatings using natural biopolymer and pollen." Thesis, KTH, Materialvetenskap, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-277932.

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Corrosion is a mechanism that highly reduces the lifetime of metals in different environments, especially in water or moisture environment. The worldwide maintenance cost due to corrosion is estimated in billions of dollars per year, and actual solutions in terms of coating usually contains toxic or environmentally harmful species. With an always increasing restriction by environmental restraints and regulations, a sustainable solution is urgently needed. Chitosan, easily obtained from chitin, the second most abundant biopolymer on earth, can be the solution to many problems. Crustacean shell waste is one of the major sources of chitin. Its resource efficiency, biocompatibility, and versatile physicochemical properties for chelation and crosslinking make chitosan a promising candidate as matrix material for biobased anticorrosive application. The purpose of the Master Thesis is to combine the properties of chitosan with the high porosity of bee pollen as anticorrosive agent carrier to obtain a fully sustainable solution for anticorrosive protection. The objective of this very ambitious project is to produce a composite material with a triple action: anticorrosive protection of metal surfaces, self-healing property of the coating and anti- biofouling activity. Results show that a biopolymer composite in forms of suspension or coatings with all desired components could be achieve. Specifically, a biopolymer nanocomposite composed of chitosan matrix, embedded with pollen grains that were loaded with anticorrosion agent 2- mercatobenzothiazole (MBT) in advance, and with zinc oxide nanoparticles have been produced. The physicochemical characterization of the biopolymer composite and its coatings, as well as electrochemical impedance spectroscopy (EIS) measurements on stainless steel plate with such coatings, suggest that a uniform and compact coating is obtained. Despite its good hydrophobicity with maximum contact angle 134.32 ± 3.84° with top coating, the chitosan nanocomposite coating is still permeable to water, partially because of the relatively big size of pollen (ca. 20 μm) that introduces gaps and interferes integrity of the coating. Therefore, a full immersion corrosion resistance is not achieved. In conclusion, phase transfer of hydrophobic pollen into hydrophilic chitosan matrix, MBT loading in pollen, ZnO encapsulation in chitosan, as well as crosslinking of chitosan, were successfully carried out. A coating based on such biopolymer nanocomposite is prepared on stainless steel and investigated on its anti-corrosion property. Future work will be choosing a proper sized pollen as a microcontainer to enhance the integrity of the coating, and eventually endow the coating with the three-in-one function, i.e., anticorrosion, antimicrobial, and self-healing.
Korrosion är en mekanism som kraftigt reducerar livslängden för metaller i olika miljöer, särskilt i vatten- eller fuktmiljö. De globala underhållskostnaderna på grund av korrosion uppskattas i miljarder dollar per år, och faktiska lösningar med avseende på beläggning innehåller vanligtvis giftiga eller miljöfarliga arter. Med en ständigt ökande begränsning genom miljörestriktioner och bestämmelser krävs det en hållbar lösning. Kitosan, den näst vanligaste biopolymeren, kan vara lösningen på många problem. Skaldjuravfall är en av de viktigaste källorna till kitosan. Dess resurseffektivitet, biokompatibilitet och mångsidiga fysikalisk-kemiska egenskaper för kelering och tvärbindning gör kitosan till en lovande kandidat som matrismaterial för biobaserade antikorrosiva applikationer. Syftet med denna masteruppsats är att kombinera egenskaperna hos kitosan med den höga porositeten hos bipollen som antikorrosivt medel för att erhålla en helt hållbar lösning för korrosionsskydd. Målet med detta mycket ambitiösa projekt är att producera ett sammansatt material med en tredubbel verkan: korrosionsskydd för metallytor, självhelande egenskap hos beläggningen och anti- biobeväxningsaktivitet. Resultaten visar att en biopolymerkomposit i form av suspension eller beläggningar med alla önskade komponenter kan uppnås. Specifikt har en biopolymer-nanokomposit sammansatt av kitosanmatris med inbäddade pollenkorn, som i förväg packats med antikorrosionsmedlet 2-mercaptobenzotiazol (MBT) och med zinkoxid-nanopartiklar, producerats. Den fysikalisk-kemiska karakteriseringen av biopolymerkompositen och dess beläggningar, liksom elektrokemiska impedansspektroskopimätningar (EIS) på rostfri stålplåt med sådana beläggningar tyder på att en enhetlig och kompakt beläggning erhålls. Trots sin goda hydrofobi med maximal kontaktvinkel 134,32 ± 3,84° med toppbeläggningen, är nanokompositbeläggningen av kitosan fortfarande permeabel för vatten, delvis på grund av den relativt stora storleken hos pollen (ca. 20 μm) som introducerar luckor och stör integriteten hos beläggningen. Därför uppnås inte en fullständig immersionskorrosionsbeständighet. Sammanfattningsvis genomfördes fasövergång av hydrofobt pollen till hydrofil kitosanmatris, MBT-packning i pollen, ZnO-inkapsling i kitosan, samt tvärbindning av kitosan med framgång. En beläggning baserad på sådan biopolymer-nanokomposit framställs på rostfritt stål och undersöks med avseende på dess korrosionsegenskaper. Framtida arbete kommer att bestå i att välja en lämplig storlek av pollen som en mikrobehållare för att förbättra beläggningens integritet, och så småningom förse beläggningen med tre-i-ett-funktionen, dvs.antikorrosion, antimikrobiell och självhelande.
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Cotterrell, M. H. "The influence of water composition on the pitting behaviour of newly developed corrosion resistant steels." Master's thesis, University of Cape Town, 1988. http://hdl.handle.net/11427/21134.

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Bibliography: pages 96-103.
The mechanisation of the working stapes in South African gold mines has required the introduction of a fundamentally new technology, hydro-power, in which machines are powered hydraulically using mine water fed from above ground. Mine water is aggressive and has a variable acidity and pH, and contains high concentrations of sulphate, chloride and nitrate ions. In order to minimise the pitting corrosion of piping and stoping machinery a compromise between selecting a suitable corrosion resistant material and treating the mine water to an acceptable level of corrosiveness is being sought.
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9

Tan, Swee Hain. "Organic corrosion inhibitors." Thesis, Tan, Swee Hain (1991) Organic corrosion inhibitors. PhD thesis, Murdoch University, 1991. https://researchrepository.murdoch.edu.au/id/eprint/333/.

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The overall aims of this thesis were to conduct a broad survey of possible organic corrosion inhibitors in near-neutral chloride solutions and to elucidate the mechanisms of such action. Altogether, 130 organic compounds were studied as possible corrosion inhibitors for pure iron, mild steel, copper and aluminium in aerated near-neutral (pH = 8.4) solutions containing 500 ppm NaCl and 100 ppm NaHCO, conditions often encountered in water-based automotive engine coolants. Inhibitor behaviour was investigated using steady-state electrochemical techniques including polarisation curves, Stern-Geary and corrosion potential (Em,) measurements. The organic compounds examined were found to be highly specific in their inhibitive action toward the metals studied. Typical examples of highly effective corrosion inhibitors were: sebacate and octanoate for pure iron; oleate and sebacate for mild steel; benzotriazole and 2-mercaptobenzothiazole for copper; and laurate and oleate for aluminium. E, was found to provide a rapid and convenient screening test for evaluating the inhibitor performance of organic compounds toward pure iron, mild steel and aluminium but was less useful for copper. Good organic inhibitors were found to act as anodic inhibitors toward pure iron and mild steel but as anodic or mixed-type inhibitors toward copper. For aluminium, the majority of the compounds studied were found to act as anodic inhibitors. However,However, it was also found that only pit initiation was inhibited, i.e. existing pits were not prevented from developing. Optical microscopy of pitted aluminium surfaces indicated their nature varied considerably with inhibition efficiency. The role of complex formation in organic corrosion inhibitors was found to vary with the metal. Complexation of either iron(I1) or iron(II1) ions was found to have an insignificant effect on mild steel. The corrosion rate of copper was found to increase with the copper(LI) complex stability, thus indicating complex formation to be the rate-determining step. For aluminium, the observed effects were found to depend on complex stability. For weak to moderate complexants, inhibitor efficiency (measured as E,,) increased with increasing complexation. However, very strong complexing agents were sufficiently stable to dissolve the aluminium oxide surface, leading to poor inhibition. Aluminium pit morphology was found, using scanning electron microscopy, to change from hemispherical in the uninhibited solution to irregular in the presence of complexing inhibitors. No simple relationships between inhibitor efficiency and molecular structure were found. However, carbon chain length, the nature of functional group(s) and their location in the molecule were found to be important but varied according to the metal. The inhibiting ability of sebacate (a straight chain C, dicarboxylate) was found not to be compromised by water movement (stirring) or pre-existing corrosion product layers. Immersion tests showed that passive film formation on mild steel in sebacate solution involved two stages and was complete only after -100 h immersion. The ion selective properties of several iron(II1) carboxylates and hydrated iron(II1) oxide films were studied by membrane potential measurements in neutral sodium chloride solutions. Some specimens were also studied by Mossbauer spectroscopy. These results show that dicarboxylates are good inhibitors toward mild steel because they form impermeable films. Poor inhibitor performance is associated with the anion selectivity of the film which in turn appears to be related to the film purity. A model is suggested for the inhibition mechanism of mild steel corrosion by dicarboxylates in aerated near-neutral chloride solutions.
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Tan, Swee Hain. "Organic corrosion inhibitors." Murdoch University, 1991. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20060818.150145.

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The overall aims of this thesis were to conduct a broad survey of possible organic corrosion inhibitors in near-neutral chloride solutions and to elucidate the mechanisms of such action. Altogether, 130 organic compounds were studied as possible corrosion inhibitors for pure iron, mild steel, copper and aluminium in aerated near-neutral (pH = 8.4) solutions containing 500 ppm NaCl and 100 ppm NaHCO,, conditions often encountered in water-based automotive engine coolants. Inhibitor behaviour was investigated using steady-state electrochemical techniques including polarisation curves, Stern-Geary and corrosion potential (Em,) measurements. The organic compounds examined were found to be highly specific in their inhibitive action toward the metals studied. Typical examples of highly effective corrosion inhibitors were: sebacate and octanoate for pure iron; oleate and sebacate for mild steel; benzotriazole and 2-mercaptobenzothiazole for copper; and laurate and oleate for aluminium. E, was found to provide a rapid and convenient screening test for evaluating the inhibitor performance of organic compounds toward pure iron, mild steel and aluminium but was less useful for copper. Good organic inhibitors were found to act as anodic inhibitors toward pure iron and mild steel but as anodic or mixed-type inhibitors toward copper. For aluminium, the majority of the compounds studied were found to act as anodic inhibitors. However,However, it was also found that only pit initiation was inhibited, i.e. existing pits were not prevented from developing. Optical microscopy of pitted aluminium surfaces indicated their nature varied considerably with inhibition efficiency. The role of complex formation in organic corrosion inhibitors was found to vary with the metal. Complexation of either iron(I1) or iron(II1) ions was found to have an insignificant effect on mild steel. The corrosion rate of copper was found to increase with the copper(LI) complex stability, thus indicating complex formation to be the rate-determining step. For aluminium, the observed effects were found to depend on complex stability. For weak to moderate complexants, inhibitor efficiency (measured as E,,) increased with increasing complexation. However, very strong complexing agents were sufficiently stable to dissolve the aluminium oxide surface, leading to poor inhibition. Aluminium pit morphology was found, using scanning electron microscopy, to change from hemispherical in the uninhibited solution to irregular in the presence of complexing inhibitors. No simple relationships between inhibitor efficiency and molecular structure were found. However, carbon chain length, the nature of functional group(s) and their location in the molecule were found to be important but varied according to the metal. The inhibiting ability of sebacate (a straight chain C, dicarboxylate) was found not to be compromised by water movement (stirring) or pre-existing corrosion product layers. Immersion tests showed that passive film formation on mild steel in sebacate solution involved two stages and was complete only after -100 h immersion. The ion selective properties of several iron(II1) carboxylates and hydrated iron(II1) oxide films were studied by membrane potential measurements in neutral sodium chloride solutions. Some specimens were also studied by Mossbauer spectroscopy. These results show that dicarboxylates are good inhibitors toward mild steel because they form impermeable films. Poor inhibitor performance is associated with the anion selectivity of the film which in turn appears to be related to the film purity. A model is suggested for the inhibition mechanism of mild steel corrosion by dicarboxylates in aerated near-neutral chloride solutions.
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Books on the topic "Corrosion resistant materials"

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J, De Renzo D., and Mellan Ibert, eds. Corrosion resistant materials handbook. 4th ed. Park Ridge, N.J., U.S.A: Noyes Data Corp., 1985.

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1911-, Sheppard Walter Lee, ed. Corrosion and chemical resistant masonry materials handbook. Park Ridge, N.J: Noyes Publications, 1986.

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Germany), Korrosionsschutzseminar (1995 Dresden. Korrosionsbeständige Werkstoffe für Chemie-, Energie- und Umwelttechnik: Korrosionsschutzseminar : Gemeinschaftsveranstaltung mit Krupp VDM GmbH, Werdohl, am 17.05.1995 in Dresden. Dresden: Das Institut, 1995.

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Germany), Korrosionsschutzseminar (1995 Dresden. Korrosionsbeständige Werkstoffe für Chemie-, Energie- und Umwelttechnik: Gemeinschaftsveranstaltung / Korrosionsschtzseminar am 22.09.1999 in Dresden. Wuppertal: TAW-Verl., 1999.

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Freeman, Richard. Corrosion and wear resistant materials for ballscrew actuator components. Wolverhampton: University of Wolverhampton, 1994.

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Cook, Ronald, and Viswanathan S. Saji. Corrosion protection and control using nanomaterials. Cambridge, UK: Woodhead Publishing, 2012.

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H, Nahm Alex, and United States. National Aeronautics and Space Administration., eds. Improved fracture toughness corrosion-resistant bearing material: Final report. [Cincinnati, Oh]: General Electric Co., Aircraft Engine Business Group, 1986.

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author, Schillmoller C. M., ed. Development of mechanized field girth welding of high-alloy corrosion-resistant pipeline materials. Toronto: Nickel Development Institute, 1992.

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European, Symposium on Corrosion Inhibitors (7th 1990 Ferrara Italy). 7th European Symposium on Corrosion Inhibitors: 153rd manifestation of the European Federation of Corrosion : proceedings, 17th-21st September 1990, Ferrara, Italy. Ferrara: Università di Ferrara, 1990.

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George, C. W. Fire retardant-caused corrosion: A 1986 field reassessment. [Ogden, Utah]: U.S. Dept. of Agriculture, Forest Service, Intermountain Research Station, 1988.

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Book chapters on the topic "Corrosion resistant materials"

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Zhang, Liwei, Kaiyuan Mei, Xiaowei Cheng, and Yongcun Feng. "Corrosion Control (I): Corrosion-Resistant Steel and Cement." In Engineering Materials, 81–98. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-2392-2_5.

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Asami, Katsuhiko, H. Habazaki, Akihisa Inoue, and Koji Hashimoto. "Recent Development of Highly Corrosion Resistant Bulk Glassy Alloys." In Materials Science Forum, 225–30. Stafa: Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-980-6.225.

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Orban, Radu L., Mariana Lucaci, Mario Rosso, and Marco Actis Grande. "NiAl Oxidation and Corrosion Resistant Coatings Obtained by Thermal Spraying." In Materials and Technologies, 273–76. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-460-x.273.

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Stinton, D. P., J. C. Mclaughlin, and L. Riester. "Fabrication and Testing of Corrosion Resistant Coatings." In 4th International Symposium on Ceramic Materials and Components for Engines, 1146–53. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2882-7_129.

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Seri, Osami. "Surface Treatment for Corrosion Resistant Aluminium Alloys by Removing Intermetallic Phases." In Materials Science Forum, 729–34. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/0-87849-408-1.729.

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Grubb, John, and James Rakowski. "Life-Cycle Costing Promotes Use of Corrosion-Resistant Alloys." In Rewas 2016: Towards Materials Resource Sustainability, 209–14. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119275039.ch30.

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Ishizaki, Takahiro, Yusaku Maruno, Kiyohiro Yabuuchi, Sosuke Kondo, and Akihiko Kimura. "Development of High Irradiation Resistant and Corrosion Resistant Oxide Dispersion Strengthened Austenitic Stainless Steels." In The Minerals, Metals & Materials Series, 605–15. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-67244-1_39.

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Ishizaki, Takahiro, Yusaku Maruno, Kiyohiro Yabuuchi, Sosuke Kondo, and Akihiko Kimura. "Development of High Irradiation Resistant and Corrosion Resistant Oxide Dispersion Strengthened Austenitic Stainless Steels." In The Minerals, Metals & Materials Series, 605–15. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-030-04639-2_39.

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Arulmurugan, B., M. Sathishkumar, K. Gokulkumar, K. Mageshkumar, P. Subramani, M. Venkateshkannan, Manikandan, and Arivazhagan. "Welding Metallurgy of Corrosion Resistant 21st Century Ni-Based Superalloy 686." In Advanced Manufacturing and Materials Science, 457–63. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-76276-0_47.

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Ishikawa, Yasunari, Jin Kawakita, and Seiji Kuroda. "Development of Corrosion and Wear Resistant Coatings by an Improved HVOF Spraying Process." In Materials Science Forum, 237–40. Stafa: Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-960-1.237.

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Conference papers on the topic "Corrosion resistant materials"

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Saal, James, Clara Nyby, John Scully, Wolfgang Windl, Christopher Taylor, John Vienna, Jie Lian, Gerald Frankel, and Joseph Ryan. "A New Paradigm for Designing Corrosion Resistant Materials." In Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.2257.

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Prakash, S. Shiva, M. K. Srinath, S. Praveen, M. Yukesh Narayanan, R. Bharath Raju, and Tauseef Ahmed. "A review on corrosion resistant materials and coatings." In INTERNATIONAL CONFERENCE ON EMERGING TRENDS IN ELECTRONICS AND COMMUNICATION ENGINEERING - 2023. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0215981.

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Bologna, Dominic J. "Corrosion Resistant Materials and Body Paint Systems for Automotive Applications." In 1986 SAE Automotive Corrosion and Prevention Conference and Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1986. http://dx.doi.org/10.4271/862015.

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Reddy, T. Ratna, Ch Indira Priyadarsini, and R. Navaneetha. "Design and analysis of impeller using corrosion resistant materials." In PROCEEDINGS OF THE 14TH ASIA-PACIFIC PHYSICS CONFERENCE. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0036476.

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Bunch, P. O., M. P. Hartmann, and T. A. Bednarowicz. "Corrosion/Galling Resistant Hardfacing Materials for Offshore Production Valves." In Offshore Technology Conference. Offshore Technology Conference, 1989. http://dx.doi.org/10.4043/6070-ms.

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Yin, Biao, Nicholas Josselyn, Ziming Zhang, Elke A. Rundensteiner, Thomas A. Considine, John V. Kelley, Berend C. Rinderspacher, Robert E. Jensen, and James F. Snyder. "MOSS: AI Platform for Discovery of Corrosion-Resistant Materials." In CIKM '23: The 32nd ACM International Conference on Information and Knowledge Management. New York, NY, USA: ACM, 2023. http://dx.doi.org/10.1145/3583780.3614748.

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Geethanjali, C. V., A. H. Riyas, and M. J. Deepa. "Hydrophobic and corrosion resistant composite hot-dip zinc coating for protection of steel." In 1st Corrosion and Materials Degradation Web Conference. Basel, Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/cmdwc2021-09969.

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Tuominen, Jari, Jonne Näkki, Juha Junkala, Juha Miettinen, Tuomo Peltola, and Petri Vuoristo. "Corrosion resistant laser coatings for hydraulic piston rods." In ICALEO® 2012: 31st International Congress on Laser Materials Processing, Laser Microprocessing and Nanomanufacturing. Laser Institute of America, 2012. http://dx.doi.org/10.2351/1.5062411.

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Smith, Cheryl Ann. "Investigation of Four Wear-Resistant Topcoat Materials with Zinc Nickel as the Corrosion-Resistant Undercoat." In Airframe Finishing, Maintenance & Repair Conference & Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1993. http://dx.doi.org/10.4271/931051.

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Razak, M. Hasbi A., and Nur Izyan Mukhtar. "Corrosion resistant alloy pipeline – Creating knowledge behind the scenes." In 4TH INTERNATIONAL CONFERENCE ON THE SCIENCE AND ENGINEERING OF MATERIALS: ICoSEM2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0029305.

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Reports on the topic "Corrosion resistant materials"

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D. K. McDonald, P. L. Daniel, and D. J. DeVault. Coal Ash Corrosion Resistant Materials Testing. Office of Scientific and Technical Information (OSTI), December 2007. http://dx.doi.org/10.2172/971251.

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D. K. McDonald, P. L. Daniel, and D. J. DeVault. Coal Ash Corrosion Resistant Materials Testing. Office of Scientific and Technical Information (OSTI), August 2003. http://dx.doi.org/10.2172/971330.

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R.B. Rebak. Selection of Corrosion Resistant Materials for Nuclear Waste Repositories. US: Yucca Mountain Project, Las Vegas, Nevada, August 2006. http://dx.doi.org/10.2172/894820.

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Stinton, D. P., T. M. Besmann, and S. Shanmugham. Development of oxidation/corrosion-resistant composite materials and interfaces. Office of Scientific and Technical Information (OSTI), June 1995. http://dx.doi.org/10.2172/115401.

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Tortorelli, P. F., P. S. Bishop, and J. R. DiStefano. Selection of corrosion-resistant materials for use in molten nitrate salts. Office of Scientific and Technical Information (OSTI), October 1989. http://dx.doi.org/10.2172/5236321.

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Stephenson, L. D., and Ashok Kumar. Corrosion-Resistant Materials for Water and Wastewater Treatment Plants at Fort Bragg. Fort Belvoir, VA: Defense Technical Information Center, June 2007. http://dx.doi.org/10.21236/ada507497.

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Zhang, Ying, and Jiahong Zhu. Development of Corrosion- and Erosion-Resistant Coatings for Advanced Ultra-Supercritical Materials. Office of Scientific and Technical Information (OSTI), December 2021. http://dx.doi.org/10.2172/1837063.

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Farmer, J., J. Choi, C. Saw, J. Haslem, D. Day, P. Hailey, T. Lian, et al. Iron-Based Amorphous-Metals: High-Performance Corrosion-Resistant Materials (HPCRM) Development Final Report. Office of Scientific and Technical Information (OSTI), March 2009. http://dx.doi.org/10.2172/950625.

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R. P. Martukanitz and S. Babu. Development of Advanced Wear and Corrosion Resistant Systems Through Laser Surface Alloying and Materials Simulations. Office of Scientific and Technical Information (OSTI), May 2007. http://dx.doi.org/10.2172/903051.

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Farmer, J., B. Brown, B. Bayles, T. Lemieux, J. Choi, L. Ajdelsztajn, J. Dannenberg, et al. DOE-DARPA High-Performance Corrosion-Resistant Materials (HPCRM), Annual HPCRM Team Meeting & Technical Review. Office of Scientific and Technical Information (OSTI), September 2007. http://dx.doi.org/10.2172/926057.

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