Academic literature on the topic 'Mechanism of cathodic reaction'

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Journal articles on the topic "Mechanism of cathodic reaction"

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ENDO, A. "Cathodic reaction mechanism for dense Sr-doped lanthanum manganite electrodes." Solid State Ionics 86-88 (July 1996): 1191–95. http://dx.doi.org/10.1016/0167-2738(96)00286-x.

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Sunarya, Yayan. "3-Mercaptopropionic Acid as Corrosion Inhibitor for Carbon Steel in CO2 Aerated 1% NaCl Solution with Buffer Control-pH." Molekul 13, no. 2 (2018): 98. http://dx.doi.org/10.20884/1.jm.2018.13.2.340.

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In this research, 3-Mercaptopropionic acid (MPA) as corrosion inhibitor of carbon steel in CO2 aerated 1% NaCl solution with buffer pH adjustment has been studied by means of electrochemical impedance (EIS) and polarization (Tafel plot). MPA was found to be an effective carbon steel inhibitor. Percentage inhibition efficiency (IE %) calculated by both Tafel plot and EIS, ranged from 85% to 90%. MPA was found to affect the cathodic processes and act as cathodic-type inhibitors. Mechanism of inhibit corrosion by adsorption mechanism leads to the formation of a protective chemisorbed film on the
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Ju, Hong, and Yan Li. "Coulostatic-Based Research on Corrosion Inhibition Mechanism of Three Inhibitors for Hot Dipped Coating Steels." Applied Mechanics and Materials 229-231 (November 2012): 87–90. http://dx.doi.org/10.4028/www.scientific.net/amm.229-231.87.

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The corrosion inhibition mechanism of three inhibitors for hot dipped coating steels in HCl acid was studied by coulostatic method. The results showed that the anodic Tafel slope ba and cathodic Tafel slope bc significantly increased with increasing of corrosion inhibitor concentration. While the corrosion current density Icorr decreases with the corrosion inhibition concentration increasing. And the inhibition efficiency increased with the inhibitor concentration. The inhibiting action of these compounds were attributed to blocking of the electrode surface by adsorption through its active cen
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Kuzminykh, Maria M., Victoria V. Panteleeva, and Anatoliy B. Shein. "CATHODIC HYDROGEN EVOLUTION ON IRON DISILICIDE. I. ALKALINE SOLUTION." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 62, no. 1 (2018): 38–45. http://dx.doi.org/10.6060/ivkkt.20196201.5745.

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The kinetics of hydrogen evolution reaction on FeSi2-electrode in 1.0 M NaOH solution has been studied using methods of polarization and impedance measurements. With the help of diagnostic criteria for the hydrogen evolution reaction mechanisms based on the analysis of the dependence of the parameters of the equivalent electric circuit on overvoltage, it was established that the reaction of hydrogen evolution on iron disilicide in the alkaline electrolyte proceeds along the discharge - electrochemical desorption route, where desorption is the rate-determining stage. Both stages are irreversibl
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Ambrosioni, Brice, Anthony Barthelemy, Dorin Bejan, and Nigel J. Bunce. "Electrochemical reduction of aqueous nitrate ion at tin cathodes." Canadian Journal of Chemistry 92, no. 3 (2014): 228–33. http://dx.doi.org/10.1139/cjc-2013-0406.

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The remediation of nitrate-contaminated water using electrochemical reduction at a tin cathode has previously been shown to give almost quantitative denitrification (removal of dissolved nitrogen species) under highly cathodic polarization. A particular focus of this project was to identify specific role(s) for tin in the reaction in the context of the previous literature. The current efficiency for denitrification was enhanced in alkaline solution, and the reaction was accelerated by the presence of small concentrations of Sn(II) salts, which are in a dynamic exchange between cathodic deposit
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Czelej, Kamil, Karol Cwieka, Juan C. Colmenares, and Krzysztof J. Kurzydlowski. "Atomistic insight into the electrode reaction mechanism of the cathode in molten carbonate fuel cells." Journal of Materials Chemistry A 5, no. 26 (2017): 13763–68. http://dx.doi.org/10.1039/c7ta02011b.

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The O-terminated octopolar NiO(111) is predicted to facilitate cathodic transformation of CO<sub>2</sub> to CO<sub>3</sub><sup>2−</sup> through sequential Mars-van Krevelen and Eley-Rideal mechanisms.
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Kuzminykh, Maria М., Viktoria V. Panteleeva, and Anatoliy B. Shein. "CATHODIC HYDROGEN EVOLUTION ON IRON DISILICIDE. II. ACIDIC SOLUTION." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 62, no. 2 (2019): 59–64. http://dx.doi.org/10.6060/ivkkt.20196202.5750.

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The kinetics of hydrogen evolution reaction on FeSi2-electrode in 0.5 M H2SO4 solution has been studied using methods of polarization and impedance measurements. With the help of diagnostic criteria for the hydrogen evolution reaction mechanisms based on the analysis of the dependence of the parameters of the equivalent electric circuit on overvoltage, it was established that the reaction of hydrogen evolution on iron disilicide in the sulfuric acid solution proceeds along the discharge - electrochemical desorption route, where desorption is the rate-determining stage. Both stages are irrevers
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He, Xiang Zhu, Wen Jun Zhang, and Yong Xiu Wang. "Electrodepositon and Properties of Ni-Diamond Composite Coatings." Advanced Materials Research 702 (May 2013): 176–80. http://dx.doi.org/10.4028/www.scientific.net/amr.702.176.

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Ni-diamond composite coatings are conducted by electrodepositon. The crystal structure and surface morphology of the composite coatings were examined with X-ray diffraction (XRD) and scanning electron microscopy (SEM) and the mechanism of Ni-diamond co-deposition is conducted by catholic polarization and cyclic voltammetry method. The result reveals that diamond particles are successfully embed in Ni matrix and the coatings have an amorphous structure. Cyclic voltammetry indicate that nickel deposition process is an irreversible electrode reaction and cathode polarization curve shift towards p
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Perevezentseva, D. O., and E. V. Gorchakov. "Electrochemical Response of Gold Nanoparticles at a Graphite Electrode." Advanced Materials Research 1040 (September 2014): 297–302. http://dx.doi.org/10.4028/www.scientific.net/amr.1040.297.

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The electrochemical activity of gold nanoparticles at graphite electrodes by the method of cyclic voltammetry is studied. In this article the nature of the supporting electrolyte, modification time of graphite electrode by gold nanoparticles and the potential range on the value of the “inverse” cathodic peak are investigated. The “inverse” cathodic peak of gold nanoparticles formed in the reaction mixture HAuCl4:Na3C6H5O7:NaBH4=1:1:4 is observed on the cathodic branch of cyclic voltamperegram at Ec = 0.05 V at graphite electrode. The mechanism of stepwise electrochemical oxidation and reductio
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Garcia-Costa, Alicia L., Andre Savall, Juan A. Zazo, Jose A. Casas, and Karine Groenen Serrano. "On the Role of the Cathode for the Electro-Oxidation of Perfluorooctanoic Acid." Catalysts 10, no. 8 (2020): 902. http://dx.doi.org/10.3390/catal10080902.

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Perfluorooctanoic acid (PFOA), C7F15COOH, has been widely employed over the past fifty years, causing an environmental problem because of its dispersion and low biodegradability. Furthermore, the high stability of this molecule, conferred by the high strength of the C-F bond makes it very difficult to remove. In this work, electrochemical techniques are applied for PFOA degradation in order to study the influence of the cathode on defluorination. For this purpose, boron-doped diamond (BDD), Pt, Zr, and stainless steel have been tested as cathodes working with BDD anode at low electrolyte conce
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Dissertations / Theses on the topic "Mechanism of cathodic reaction"

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Ina, Toshiaki. "Study on Cathodic Reaction Mechanism of All Solid State Electrochemical Devices." Kyoto University, 2012. http://hdl.handle.net/2433/157658.

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Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(人間・環境学)<br>甲第16947号<br>人博第590号<br>新制||人||141(附属図書館)<br>23||人博||590(吉田南総合図書館)<br>29622<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授 内本 喜晴, 教授 杉山 雅人, 教授 田部 勢津久, 准教授 藤原 直樹, 准教授 雨澤 浩史<br>学位規則第4条第1項該当
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Xiao, Yao. "Analysis for reaction mechanism of cathode materials for lithium-sulfur batteries." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263747.

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京都大学<br>新制・課程博士<br>博士(人間・環境学)<br>甲第23286号<br>人博第1001号<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授 内本 喜晴, 教授 田部 勢津久, 教授 高木 紀明<br>学位規則第4条第1項該当<br>Doctor of Human and Environmental Studies<br>Kyoto University<br>DFAM
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Williams, Robert Earl Jr. "Simulation and Characterization of Cathode Reactions in Solid Oxide Fuel Cells." Diss., Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/16309.

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In this study, we have developed a dense La0.85Sr0.15MnO3-δ (LSM) Ce0.9Gd0.1O1.95 (GDC) composite electrode system for studying the surface modification of cathodes. The LSM and GDC grains in the composite were well defined and distinguished using energy dispersive x-ray (EDX) analysis. The specific three-phase boundary (TPB) length per unit electrode surface area was systematically controlled by adjusting the LSM to GDC volume ratio of the composite from 40% up to 70%. The TPB length for each tested sample was determined through stereological techniques and used to correlate the cell perfor
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Phillips, Janice Paige. "Rearrangements of Radical Anions Generated from Cyclopropyl Ketones." Diss., Virginia Tech, 1998. http://hdl.handle.net/10919/40178.

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Cyclopropyl-containing substrates have been frequently utilized as "probes" for the detection of SET pathways in organic and biorganic systems. These reactions are based on the cyclorpropylcarbinyl - homoallyl rearrangement, which is fast and essentially irreversible. The implicit assumption in such studies is that if a "radical" species is produced, it will undergo ring opening. We have found that there are two important factors to consider in the design of SET probes: 1) ring strain, the thermodynamic driving force for the rearrangement, and 2) resonance energy, which may
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Tuerxun, Feilure. "Elucidation of reaction mechanism at the anode/electrolyte interface and cathode material for rechargeable magnesium battery." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263749.

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京都大学<br>新制・課程博士<br>博士(人間・環境学)<br>甲第23288号<br>人博第1003号<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授 内本 喜晴, 教授 高木 紀明, 教授 中村 敏浩<br>学位規則第4条第1項該当<br>Doctor of Human and Environmental Studies<br>Kyoto University<br>DFAM
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Komatsu, Hideyuki. "Elucidation of Reaction Mechanism for High Energy Cathode Materials in Lithium Ion Battery using Advanced Analysis Technologies." Kyoto University, 2019. http://hdl.handle.net/2433/242753.

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Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(人間・環境学)<br>甲第21876号<br>人博第905号<br>新制||人||216(附属図書館)<br>2018||人博||905(吉田南総合図書館)<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授 内本 喜晴, 教授 田部 勢津久, 教授 吉田 鉄平<br>学位規則第4条第1項該当
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Fu, Qiang [Verfasser], and H. [Akademischer Betreuer] Ehrenberg. "Reaction mechanism study of vanadium pentoxide as cathode material for beyond-Li energy storage via in operando techniques / Qiang Fu ; Betreuer: H. Ehrenberg." Karlsruhe : KIT-Bibliothek, 2019. http://d-nb.info/1189212447/34.

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Herle, Jan van Van herle Jan Van herle Jan Van herle Jan. "Oxygen reduction reaction mechanisms at solid fuel cell cathodes /." [S.l.] : [s.n.], 1993. http://library.epfl.ch/theses/?nr=1187.

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Сачанова, Юлія Іванівна. "Електрохімічне формування покривів сплавами і композитами Fe–Co–Mo(MoOₓ)". Thesis, Національний технічний університет "Харківський політехнічний інститут", 2020. http://repository.kpi.kharkov.ua/handle/KhPI-Press/43990.

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Дисертація на здобуття наукового ступеня кандидата технічних наук за спеціальністю 05.17.03 – Технічна електрохімія. – Національний технічний уні-верситет “Харківський політехнічний інститут”, Харків, 2019. Дисертаційну роботу присвячено розробці технології електроосадження функціональних покривів сплавами заліза з кобальтом і молібденом з комплек-сних цитратних електролітів. За результатами аналізу іонних рівноваг і кінетичних закономірностей встановлено, що молібден відновлюється у сплав з ферумом та кобальтом до металевого стану з гетероядерних комплексів через утворення проміжних сполук як
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Rattakham, Krittin. "Mechanism of Cathodic Prevention of Carbon Steel in Concrete." Scholar Commons, 2017. http://scholarcommons.usf.edu/etd/6630.

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In this work, I aim to clarify the mechanism that allows steel to attain higher chloride threshold as it is cathodically polarized. Specifically, I seek to provide empirical information on whether an intrinsic (predominantly interfacial effects of polarization) or an extrinsic (predominantly concentration changes due to polarization) mechanism may be dominant in the beneficial effect of polarization. I carried out this experiment with 12 identical concrete specimens, each with a cast-in steel plate, constantly exposed them to high-chloride environment. The specimens were divided into 4 triplic
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Books on the topic "Mechanism of cathodic reaction"

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Halevi, E. Amitai, ed. Orbital Symmetry and Reaction Mechanism. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-83568-1.

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Halevi, E. Amitai. Orbital symmetry and reaction mechanism: The OCAMS view. Springer-Verlag, 1992.

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Crowley, John N. A study of reaction mechanism by matrix isolation/FTIR spectroscopy. University of East Anglia, 1987.

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Gao, Ying. Investigations on the mechanism of the Belousov-Zhabotinsky oscillating reaction. Cuvillier Verlag, 1994.

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Arve, Kalle. Catalytic diesel exhaust aftertreatment: From reaction mechanism to reactor design. Åbo Akademis förlag, 2005.

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Dhatt, Harjot S. The mechanism and nonlinear dynamics of the chlorite-lodide reaction. Laurentian University, 1996.

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Bittker, David A. Detailed mechanism for oxidation of benzene. National Aeronautics and Space Administration, 1990.

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Grzybowski, Bartosz A. Chemistry in motion: Reaction-diffusion systems for micro- and nanotechnology. Wiley, 2009.

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Wilkins, Ralph G. Kinetics and mechanism of reactions of transition metal complexes. 2nd ed. VCH, 1991.

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Lurmann, Frederick W. A surrogate species chemical reaction mechanism for urban-scale air quality simulation models. U.S. Environmental Protection Agency, Atmospheric Sciences Research Laboratory, 1987.

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Book chapters on the topic "Mechanism of cathodic reaction"

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Krishtalik, L. I. "Mechanism of an Elementary Act and the Kinetics of the Cathodic Evolution of Hydrogen." In Charge Transfer Reactions in Electrochemical and Chemical Processes. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-8718-3_6.

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Yamada, Atsuo. "Olivine Phosphate Cathode Materials, Reactivity and Reaction Mechanisms." In Batteries for Sustainability. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-5791-6_14.

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Minges, Mary V., Claire J. Starrs, and J. Christopher Perry. "Reaction Formation (Defense Mechanism)." In Encyclopedia of Personality and Individual Differences. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-24612-3_1420.

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Saha, Goutam Kumar. "Mechanism of Allergic Reaction." In Dust Allergy: Cause & Concern. Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-1825-1_4.

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García Melchor, Max. "The Negishi Reaction Mechanism." In A Theoretical Study of Pd-Catalyzed C-C Cross-Coupling Reactions. Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01490-6_4.

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Minges, Mary V., Claire J. Starrs, and J. Christopher Perry. "Reaction Formation (Defense Mechanism)." In Encyclopedia of Personality and Individual Differences. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-28099-8_1420-1.

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Yang, Ruixin, Chun Wang, and Zonglin Jiang. "Genetic Algorithm Applied in Optimizing Reaction Mechanism Based on Reduced Reaction Mechanism." In Advances in Natural Computation, Fuzzy Systems and Knowledge Discovery. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-70665-4_196.

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Brown, J. B. "Mechanism of the Kober Reaction." In Ciba Foundation Symposium - Estimation of Steroid Hormones (Book I of Colloquia on Endocrinology, Vol. 2). John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470718773.ch12.

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Zhao, Zuzhen, and Pei Kang Shen. "Mechanism of Oxygen Reduction Reaction." In Electrochemical Oxygen Reduction. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6077-8_2.

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Yamada, Atsuo. "Olivine Olivine Phosphate Cathode Materials olivine phosphate cathode materials , Reactivity and Reaction Mechanisms." In Encyclopedia of Sustainability Science and Technology. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0851-3_499.

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Conference papers on the topic "Mechanism of cathodic reaction"

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Yunovich, Mark, and Neil G. Thompson. "AC Corrosion: Mechanism and Proposed Model." In 2004 International Pipeline Conference. ASMEDC, 2004. http://dx.doi.org/10.1115/ipc2004-0574.

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Corrosion caused by the discharge of 60 Hz AC current from a pipeline in a high voltage AC (HVAC) corridor has been discussed and studied over the past 20 or more years. More recent studies in Europe have specifically addressed these corrosion issues following several failures attributed to the presence of AC discharge from the pipeline. Very few corrosion failures in North America have been specifically attributed to what is termed AC-enhanced corrosion (ACEC). One missing area of research is well-controlled laboratory experiments in soil environments. This study proposed a mechanism of ACEC
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Tarhini, Ali A., and Ramsey F. Hamade. "Cathodic Disbondment of Rubber/Steel Adhesive Bonds Modeled as Liquid-Solid Reactions." In ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-63307.

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Under cathodic conditions, rubber/steel adhesive bonded joints have been documented to ‘weaken’ due to attack by the generated alkali. If this were to occur under the action of cleavage mechanical loads, the bonds are likely to completely ‘delaminate’ causing the bonded constituents to physically separate. These two modes of disbondment are referred to as ‘weakening’ and ‘delamination’, respectively. Previously, Hamade and coworkers have implemented empirical and semi-empirical approaches to modeling cathodic disbondment of adhesive joints. Here, a method is presented to simulate bond weakenin
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Saji, Genn. "Degradation of Aged Plants by Corrosion: Radiation-Induced Corrosion Cells Inducing “Long-Cell” Action." In 17th International Conference on Nuclear Engineering. ASMEDC, 2009. http://dx.doi.org/10.1115/icone17-75712.

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In the previous papers, the author has established various ‘long cell’ corrosion configurations that should exist in nuclear power plants. With these corrosion mechanisms in place, the plant can be characterized as an assembly of gigantic short-circuited electrical batteries, inducing electrochemical corrosion at localized anodic sites. If these corrosion cells are involved at nuclear power plants, macroscopic electrochemical potential differences must be demonstrated between anodic sites where dissolution of metal (i.e. corrosion) is taking place and cathodic sites where deposition (also call
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Saji, Genn. "“Long-Cell Action” Corrosion: A Basic Mechanism Hidden Behind Components Degradation Issues in Nuclear Power Plants." In 14th International Conference on Nuclear Engineering. ASMEDC, 2006. http://dx.doi.org/10.1115/icone14-89350.

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In spite of industries’ effort over the last 40 years, corrosion-related issues continue to be one of the largest unresolved problems for nuclear power plants worldwide. There are several types of strange corrosion phenomena from the point of view of our current understanding of corrosion science established in other fields. Some of these are IGSCC, PWSCC, AOA, and FAC (Erosion-Corrosion). Through studying and coping with diverse corrosion phenomena, the author believes that they share a common basis with respect to the assumed corrosion mechanism (e.g., ‘local cell action’ hypothesis). In gen
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Baek, Seung-Wook, Joongmyeon Bae та Jung Hyun Kim. "Oxygen Reduction Mechanism at Sm0.5Sr0.5CoO3−δ/Sm0.2Ce0.8O1.9 Composite Cathode for Solid Oxide Fuel Cell". У ASME 2008 6th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2008. http://dx.doi.org/10.1115/fuelcell2008-65059.

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The oxygen reduction mechanism at porous Sm0.5Sr0.5CoO3−δ/Sm0.2Ce0.8O1.9 composite cathode, in which Sm0.5Sr0.5CoO3−δ is a perovskite type mixed ionic and electronic conductor (MIEC), was studied with respect to the oxygen partial pressure and temperature. Symmetric half cells with Sm0.2Ce0.8O1.9 electrolyte were prepared, and cathode behavior was measured by using electrochemical impedance spectroscopy at frequency range of 0.1Hz∼5MHz and temperature range of 400∼900°C. Oxygen partial pressure range for the measurement was from 0.0002 to 1atm. In present research, reaction model based on the
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Alqahtani, Noora, Jiahui Qi, Aboubakr M. Abdullah, Nicholas J. Laycock, and Mary P. Ryan. "The Formation of Sulfide Scales on Carbon Steel in Saturated H2S." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2020. http://dx.doi.org/10.29117/quarfe.2020.0057.

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There are three contributing elements of corrosion of Carbon Steel in H₂ S environment: the effect of H2S on water chemistry; electrochemical reactions of the bare iron surface (both anodic and cathodic processes); and the formation and growth of corrosion product layers. The electrochemical reaction commonly contains three stages: first, the reactant transported from the solution (bulk) to the metal surface; then the transfer of the charge reaction on the surface, followed by the reaction product transported away from the iron surface to the bulk solution or the formation and development of t
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Izzo, John R., Kyle N. Grew, and Wilson K. S. Chiu. "Strontium-Doped Lanthanum Manganate Cathode Degradation Due to a Decomposed Hydrogen Peroxide Oxidant Feed Stream." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-68424.

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Decomposed hydrogen peroxide (H2O2) contains excess moisture and stabilizers that can deteriorate SOFC performance and durability markedly in the cathode. A numerical study is performed for a strontium-doped lanthanum manganate and yttria stabilized zirconia (LSM-YSZ) composite cathode using an oxidant stream consisting of a 20% O2 and 80% H2O mixture to study the detailed reaction mechanism and local transport and polarization phenomena. Specifically the 1-D cathode model couples multi-component gas and charge transport with an oxygen reduction mechanism. The model is validated with data from
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Fischer, Katharina, and Joerg R. Seume. "Location and Magnitude of Heat Sources in Solid Oxide Fuel Cells." In ASME 2006 4th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2006. http://dx.doi.org/10.1115/fuelcell2006-97167.

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The correct prediction of the temperature distribution is a prerequisite for the reliable determination of species and current distributions in any solid oxide fuel cell (SOFC) model. It is even more crucial if the model is intended for the analysis of thermo-mechanical stresses. This paper addresses the different mechanisms of heat generation and absorption in the fuel cell. Particular attention is paid to the heating associated with the oxidation of hydrogen, which is commonly assigned to the interface between electrolyte and anode in SOFC modeling. But for a detailed determination of the te
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Saji, Genn. "Radiation-Induced Electrolytic Corrosion of LWRS: (Part 1) — Basic Mechanism and Implications in Degradation Phenomena." In 2016 24th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icone24-60894.

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The author recently found that there should exist a “radiation-induced electrolytic (RIE)” mechanism in the reactor water inducing severe interaction between structural materials and their environments in aged LWRs. This mechanism was identified while trying to theoretically reconstruct the potential differences observed in two in-pile test loops; NRI-Rez in Czech Republic and INCA Loop in Sweden. These results are indicating that the in-core potential is approximately 0.1/0.4volt higher, in BWR(NWC)/PWR water chemistry respectively, when compared to the out-core regions. Through modeling stud
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Izzo, John R., Kyle N. Grew, and Wilson K. S. Chiu. "Effect of Excess Moisture on an Oxygen Reduction Reaction Mechanism in the Yttria Stabilized Zirconia and Strontium-Doped Lanthanum Manganite SOFC Composite Cathode." In ASME 2009 7th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2009. http://dx.doi.org/10.1115/fuelcell2009-85124.

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Air-Independent solid oxide fuel cell (SOFC) systems are primarily used in naval applications. In this study a decomposed hydrogen peroxide (H2O2) stream is used as the oxidant. The fully decomposed diluted H2O2 oxidant stream contains 20% O2 and 80% H2O, and this water content is the basis for the studies performed. A computational model has been developed that couples local gas and charge transport with a detailed oxygen reduction mechanism and considers surface coverages in the presence of excess moisture. The model is used to study the detailed reaction mechanism and the performance of the
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Reports on the topic "Mechanism of cathodic reaction"

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Schulze, Roland K. Uranium-hydrogen reaction mechanism and numerical model. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1617331.

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Ziaul Huque. Mathematically Reduced Chemical Reaction Mechanism Using Neural Networks. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/947008.

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Nelson Butuk. Mathematically Reduced Chemical Reaction Mechanism Using Neural Networks. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/875887.

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Nelson Butuk. Mathematically Reduced Chemical Reaction Mechanism Using Neural Networks. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/902508.

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Nelson Butuk. Mathematically Reduced Chemical Reaction Mechanism Using Neural Networks. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/881862.

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Hartman, F. C. Rubisco Mechanism: Dissection of the Enolization Partial Reaction. Final Report. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/824531.

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Rice, Betsy M., William Mattson, John Grosh, and S. F. Trevino. A Molecular Dynamics Study of Detonation. 2. The Reaction Mechanism. Defense Technical Information Center, 1996. http://dx.doi.org/10.21236/ada305237.

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Longfellow, C. A. Reaction mechanism studies of unsaturated molecules using photofragment translational spectroscopy. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/266645.

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McNicholas, Michael. On the mechanism of the Diels-Alder reaction--dimerization of trans-phenylbutadiene. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.972.

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Wang, Hai. Development of a Comprehensive and Predictive Reaction Mechanism of Liquid Hydrocarbon Combustion. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada464234.

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