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Relevant bibliographies by topics / Reduction (Chemistry) Electrolytic reduction

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Academic literature on the topic 'Reduction (Chemistry) Electrolytic reduction'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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Journal articles on the topic "Reduction (Chemistry) Electrolytic reduction"

1

Knittel, Dierk, and V. Suryanarayana Rao. "Electrolytic reduction of azidochalcones." Monatshefte für Chemie - Chemical Monthly 117, no. 10 (October 1986): 1185–93. http://dx.doi.org/10.1007/bf00811331.

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Merica, Simona G., Wojceich Jedral, Susan Lait, Peter Keech, and Nigel J. Bunce. "Electrochemical reduction and oxidation of DDT." Canadian Journal of Chemistry 77, no. 7 (July 1, 1999): 1281–87. http://dx.doi.org/10.1139/v99-113.

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Electrolysis has been studied as a possible method to treat DDT wastes. In methanol, the major process was dehydrochlorination to DDE followed by further reduction. In an aqueous emulsion containing 1% heptane and 0.1% Triton SP-175®, DDT was reduced at a deposited lead electrode with sodium sulphate as the supporting electrolyte by sequential hydrodechlorination of the aliphatic chlorine atoms. An excellent material balance was achieved, but the current efficiency was poor, even at low current densities. Electrooxidation of DDT was also investigated; in aqueous solutions or emulsion, little oxidation occurred because of competing oxidation of water at the highly positive potentials needed to oxidize DDT. In acetonitrile, electrooxidation occurred with high current efficiency by way of "electrochemical combustion" of DDT and its intermediate oxidation products to CO2. We conclude that development of an electrolytic technology for destroying DDT wastes is unlikely.Key words: electroreduction, electrooxidation, voltammetry, surfactant media.

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Li, Tengfei, Yang Cao, Jingfu He, and Curtis P. Berlinguette. "Electrolytic CO2 Reduction in Tandem with Oxidative Organic Chemistry." ACS Central Science 3, no. 7 (June 28, 2017): 778–83. http://dx.doi.org/10.1021/acscentsci.7b00207.

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Ouyang, Yixin, Yehui Zhang, Peter S. Rice, Li Shi, Jinlan Wang, and P. Hu. "Electrochemical CO2 reduction: water/catalyst interface versus polymer/catalyst interface." Journal of Materials Chemistry A 9, no. 32 (2021): 17474–80. http://dx.doi.org/10.1039/d1ta04867h.

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Alkaline polymer electrolyte electrolytic cells (APEECs) have the potential to replace aqueous-phase CO2 electrolyzer. Full reaction kinetics at polymer/copper interface is obtained to present a fundamental understanding of the superiority of APEECs.

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Weekes, David M., Danielle A. Salvatore, Angelica Reyes, Aoxue Huang, and Curtis P. Berlinguette. "Electrolytic CO2 Reduction in a Flow Cell." Accounts of Chemical Research 51, no. 4 (March 23, 2018): 910–18. http://dx.doi.org/10.1021/acs.accounts.8b00010.

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Hlavatý, Jaromír. "Electrolytic reduction of o-nitrobenzyl thiocyanate in buffered solutions on mercury." Collection of Czechoslovak Chemical Communications 50, no. 1 (1985): 33–41. http://dx.doi.org/10.1135/cccc19850033.

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The o-nitrobenzyl thiocyanate (I) behaves differently on the DME and on a large mercury pool electrode. Polarography did not give a sufficiently clear explanation of the reaction mechanism, only the preparative experiments yielded useful results. Whereas polarographic curves in solutions of Britton-Robinson buffer system with 50% by vol. ethanol exhibit two cathodic waves within the pH region 1-12, corresponding according to their height ratio to an uptake of 4 e and 2 e respectively, the controlled potential preparation electrolysis (CPE) and coulometry results indicate a more complicated reaction path. In the CPE carried out at the concentration of I 1 . 10 -2 mol/l the electroreductive splitting of CH2-SCN occurs as the first step. Nitrobenzyl radicals so formed react in the follow-up dimerization resulting in dibenzyl or toluene structures. Simultaneously or at a later stage the completion of the electrolytic reduction of the nitro group proceeds to the hydroxylamino group. In solution of 9 > pH > 1 the CPE of nitro compound I takes place by an ECEC mechanism yielding dibenzodiazocine III, its N-oxide IV and 2,2'-dimethylazoxybenzene (V). In course of preparative electrolysis in strongly acidic medium 2-amino-benzo(l,3)-thiazine-l-oxide (II) is formed by an EC mechanism.

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Moore, William, Wade Henke, Davide Lionetti, Victor Day, and James Blakemore. "Single-Electron Redox Chemistry on the [Cp*Rh] Platform Enabled by a Nitrated Bipyridyl Ligand." Molecules 23, no. 11 (November 2, 2018): 2857. http://dx.doi.org/10.3390/molecules23112857.

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[Cp*Rh] complexes (Cp* = pentamethylcyclopentadienyl) are attracting renewed interest in coordination chemistry and catalysis, but these useful compounds often undergo net two-electron redox cycling that precludes observation of individual one-electron reduction events. Here, we show that a [Cp*Rh] complex bearing the 4,4′-dinitro-2,2′-bipyridyl ligand (dnbpy) (3) can access a distinctive manifold of five oxidation states in organic electrolytes, contrasting with prior work that found no accessible reductions in aqueous electrolyte. These states are readily generated from a newly isolated and fully characterized rhodium(III) precursor complex 3, formulated as [Cp*Rh(dnbpy)Cl]PF6. Single-crystal X-ray diffraction (XRD) data, previously unavailable for the dnbpy ligand bound to the [Cp*Rh] platform, confirm the presence of both [η5-Cp*] and [κ2-dnbpy]. Four individual one-electron reductions of 3 are observed, contrasting sharply with the single two-electron reductions of other [Cp*Rh] complexes. Chemical preparation and the study of the singly reduced species with electronic absorption and electron paramagnetic resonance spectroscopies indicate that the first reduction is predominantly centered on the dnbpy ligand. Comparative cyclic voltammetry studies with [NBu4][PF6] and [NBu4][Cl] as supporting electrolytes indicate that the chloride ligand can be lost from 3 by ligand exchange upon reduction. Spectroelectrochemical studies with ultraviolet (UV)-visible detection reveal isosbestic behavior, confirming the clean interconversion of the reduced forms of 3 inferred from the voltammetry with [NBu4][PF6] as supporting electrolyte. Electrochemical reduction in the presence of triethylammonium results in an irreversible response, but does not give rise to catalytic H2 evolution, contrasting with the reactivity patterns observed in [Cp*Rh] complexes bearing bipyridyl ligands with less electron-withdrawing substituents.

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Gilbert, David M., and Tom C. Sale. "Sequential Electrolytic Oxidation and Reduction of Aqueous Phase Energetic Compounds." Environmental Science & Technology 39, no. 23 (December 2005): 9270–77. http://dx.doi.org/10.1021/es051452k.

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Yan, Xiao Y., and Derek J. Fray. "Direct electrolytic reduction of solid alumina using molten calcium chloride-alkali chloride electrolytes." Journal of Applied Electrochemistry 39, no. 8 (February 11, 2009): 1349–60. http://dx.doi.org/10.1007/s10800-009-9808-3.

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Xie, Kaiyu, and Ali Reza Kamali. "Electro-reduction of hematite using water as the redox mediator." Green Chemistry 21, no. 2 (2019): 198–204. http://dx.doi.org/10.1039/c8gc02756k.

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Dissertations / Theses on the topic "Reduction (Chemistry) Electrolytic reduction"

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Su, Yuhlong Oliver. "Electrochemistry of metalloporphyrins and their catalytic reduction of oxygen at carbon electrodes /." The Ohio State University, 1985. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487260135354882.

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Dai, Congxia. "An advanced data acquisition system & noise analysis on the aluminum reduction process." Morgantown, W. Va. : [West Virginia University Libraries], 2003. http://etd.wvu.edu/templates/showETD.cfm?recnum=2850.

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Thesis (M.S.)--West Virginia University, 2003.
Title from document title page. Document formatted into pages; contains ix, 82 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 75-78).

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Cuzan, Olesea. "Synthesis and characterization of new transition metal complexes for catalytic oxidation and electrolytic proton reduction." Thesis, Aix-Marseille, 2016. http://www.theses.fr/2016AIXM4356/document.

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De nos jours, la capacité à synthétiser de nouveaux catalyseurs métallique bioinspirés pour améliorer et élargir le spectre d'activité catalytique est d’une importance capitale pour une chimie respectueuse de notre environnement.Cette thèse se concentre sur la conception de nouveaux complexes de métaux de transition (cuivre et palladium) basés sur deux classes différentes de ligands organiques : les benzotriazolyle-phénolates et les phosphonates. La synthèse et la caractérisation de nouveaux composés a été réalisée par différentes méthodes physico-chimiques (électrochimie, EPR, UV-vis, IR, cristallographie aux rayons X) et la chimie théorique. La génération et la caractérisation des différentes espèces réduites et oxydées nous ont aidés dans la détermination des mécanismes possible. Les composés obtenus ont été utilisés avec succès comme catalyseurs dans divers procédés tels que: la production d'hydrogène, l'oxydation d'alcool et le clivage d'ADN
Nowadays, the ability to synthesize new bioinspired metal catalysts to improve and broaden the spectrum of catalytic activity is of paramount importance for sustainable chemistry respectful for our environment. This thesis is focused on the design of transition metal complexes (copper and palladium) based on two different classes of organic ligands: benzotriazolyl-phenolates and phosphonates.Different original complexes based on palladium and copper were synthetized from benzotriazolyl-phenolate and phosphonates ligands. The characterization of the new compounds was performed by different physical and physico-chemical methods (electrochemistry, EPR, UV-vis, IR, X-ray crystallography) and quantum chemistry. The generation and characterization of different reduced and oxidized species helped us in the possible mechanisms determination. The obtained compounds were successfully employed as catalysts in different processes as: hydrogen production, alcohol oxidation and DNA cleavage

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Cherednik, Avital, Anders Abrahamsson, and Bjarne Falk. "Oxygen Reduction Catalysts in Alkaline Electrolyte." Thesis, KTH, Skolan för kemi, bioteknologi och hälsa (CBH), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-277116.

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Alkaline fuel cells are a promising technology, with their sturdy design and many applications they are held back mostly by their cost. By introducing a catalyst, the activation energy of the cell can be reduced to an overcomable amount. Unfortunately, due to the high cost and sparse availability of the most used catalyst metal today, platinum, it has become apparent that a new suitable catalyst must be found in order to make the fuel cells economically feasible. Silver and palladium have been proposed as promising alternatives, sharing a majority of the traits but with a fraction of the cost. The original aim of this project was to study the performance of electrodes in an alkaline electrolyte loaded with different ratios of palladium and silver. However, due to the COVID-19 situation the project was not able to be completed and the aim of the project changed. The new aim was divided into two parts. The first one being to study how the initial concentration of silver ions affects the size of the obtained particles. This was achieved by a radiolysis-based method of synthesis in an aqueous solution. The second aim was to study the performance of the electrodes loaded with different amounts of silver and different average particle size. However, this part was not possible to conduct either. Therefore, results from a previous study performed by I. L. Soroka et al. was used for discussion. The results point towards a lower initial concentration achieving a smaller average particle size and a lower loading of catalyst on the electrode can be compensated by a smaller average particle size of the catalyst.

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Zhang, Yun. "Mass Spectrometric Analysis of Thiol Proteins/Peptides Following Selenamide Derivatization And Electrolytic Reduction of Disulfide Bonds." Ohio University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1347395762.

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Wang, Vincent Cho-Chien. "New insights into enzymatic CO₂ reduction using protein film electrochemistry." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:f1061854-f6b8-4562-81e0-968c80e1da3a.

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Carbon monoxide dehydrogenase (CODH) is known to catalyze CO oxidation and CO₂ reduction reversibly with the minimal overpotential. A great advantage of protein film electrochemistry (PFE) is its ability to probe catalysis over a wide range of potentials, especially in the low potential region required for CO₂ reduction. CODH I and CODH II from Carboxydothermus hydrogenoformans(Ch) and the composite enzyme acetyl-CoA synthase/carbon monoxide dehydrogenase (ACS/CODH) from Moorella thermoacetica(Mt) are intensively studied throughout this thesis. The different catalytic redox-states in CODH, C_ox (inactive state), C_red1 (for CO oxidation) and C_red2 (for CO₂ reduction) as characterized by spectroscopy, are studied by PFE in the presence of substrate-mimic inhibitors. Cyanide, isoelectronic with CO, mainly inhibits CO oxidation, whereas cyanate, isoelectronic with CO₂, mainly targets CO₂ reduction. Sulfide inhibits CODH rapidly when the potential is more positive than −50 mV, which suggests that sulfide reacts to form a state at the oxidation level of C_ox in CODH and is not an activator for CODH catalysis as suggested before. Thiocyanate only partially inhibits CO oxidation. No inhibition of CODH by azide is detected, which is in contrast with previous studies with ACS/CODH_Mt. The main differences between CODH I_Ch and CODH II_Ch are the stronger CO product inhibition and inhibition of CODH II_Ch by cyanide. These discoveries might shed light on the possible role of CODH II_{Ch,/sub> in biological systems. In comparison with bidirectional (reversible) electrocatalysis by CODH I_Ch and CODH II_Ch, only unidirectional electrocatalysis for CO oxidation by ACS/CODH_Mt is observed with an overpotential of 0.1 V and the electrocatalytic current is much smaller. In order to identify whether ACS influences the performance of CODH, several chemical reagents, such as sodium dodecyl sulfate (which separates CODH and ACS partially), 1, 10-phenanthroline, (which inhibits the active site in ACS) and acetyl-CoA (the product of the reaction carried out by ACS/CODH_Mt) are added. However, we have yet to observe any electrocatalytic current from CO₂ reduction. Inhibition of ACS/CODH_Mt by cyanide, cyanate and azide is consistent with previous studies by spectroscopy. Oxygen attack toward the active site in CODH is proved by cyanide protection. The inactive state, C_ox can prevent oxygen attack and reductive reactivation restores CODH activity. In contrast, oxygen damages the active site irreversibly when CODH is in the C_red1 state. The new substrate, nitrous oxide (N₂O), isoelectronic with CO₂, is reduced by CODH and acts as the suicide substrate. Finally, hydrogen formation in the direction of CO oxidation and formate formation in the direction of CO₂ reduction by CODH are detected. The small solvent kinetic isotope effect is observed in CO oxidation. These findings suggest metal-hydride should play a role in CODH catalysis, which might provide a new direction to design better catalysts for CO₂ reduction.}

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Woolerton, Thomas William. "Development of enzymatic H2 production and CO2 reduction systems." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:393741ac-94b1-4d56-b680-d9a434db77e2.

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One of today’s most pressing scientific challenges is the conception, development and deployment of renewable energy technologies that will meet the demands of a rapidly increasing population. The motivation is not only dwindling fossil fuel reserves, but also the necessary curtailment of emissions of the greenhouse gas carbon dioxide (a product of burning fossil fuels). The sun provides a vast amount of energy (120,000 TW globally), and one major challenge is the conversion of a fraction of this energy into chemical energy, thereby allowing it to be stored. Dihydrogen (H₂) that is produced from water is an attractive candidate to store solar energy (a ‘solar fuel’), as are high energy carbon-containing molecules (such as CO) that are formed directly from carbon dioxide. One key aspect is the development of catalysts that are able to offer high rates and efficiencies. In biology, some microbes acquire energy from the metabolism of H₂ and CO. The biological catalysts - enzymes - that are responsible are hydrogenases (for the oxidation of H₂ to protons); and carbon monoxide dehydrogenases (CODHs, for the oxidation of CO to CO₂). These redox enzymes, containing nickel and iron as the only metals, are extraordinary in terms of their catalytic characteristics: many are fully reversible catalysts and offer very high turnover frequencies (thousands per second are common), with only tiny energy input requirements. This Thesis uses a hydrogenase from the bacterium Escherichia coli, and two CODHs from the bacterium Carboxydothermus hydrogenoformans, as the catalysts in H2 production and CO₂ reduction systems. Chapter 3 describes the concept and development not of a solar fuel system, but of a device that catalyses the water-gas shift reaction (the reaction between CO and water to form H₂ and CO₂) - a process of major industrial importance for the production of high purity H₂. Chapters 4, 5 and 6 detail photochemical CO₂ reduction systems that are driven by visible light. These systems, operating under mild, aqueous conditions, involve CODHs attached either to TiO₂ nanoparticles that are sensitised to visible light by the co-attachment of a ruthenium-based dye complex, or to cadmium sulfide nanomaterials that, having a narrow band gap, are inherently photoexcitable by visible light. The motivation here is not the construction of technological devices; indeed, the enzymes that are used are fragile, highly sensitive to oxygen, and impossible to scale to industrial levels. Rather, the drivers are those of scientific curiosity (can the incorporation of these remarkable biological catalysts enable the creation of outstanding solar fuel devices?), and of producing systems that serve as benchmarks and inspiration for the development of fully synthetic systems that are robust and scalable.

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Strobl, Jonathan R. "ELECTROCATALYTIC STUDIES OF SUPEROXIDE AS AN INTERMEDIATE FOR THE OXYGEN REDUCTION REACTION IN BASIC ELECTROLYTES & THE REDUCTION OF SELENATE ON UNDERPOTENTIAL DEPOSITED Cu ON Au." Case Western Reserve University School of Graduate Studies / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1595623881870564.

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Green, Robert David. "Carbon Dioxide Reduction on Gadolinia-Doped Ceria Cathodes." Case Western Reserve University School of Graduate Studies / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=case1232574534.

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Zhu, Huanfeng. "Experimental and Theoretical Aspects of Electrode Electrolyte Interfaces." Cleveland, Ohio : Case Western Reserve University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1259680393.

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Thesis(Ph.D.)--Case Western Reserve University, 2010
Title from PDF (viewed on 2009-12-30) Department of Chemistry Includes abstract Includes bibliographical references and appendices Available online via the OhioLINK ETD Center

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Books on the topic "Reduction (Chemistry) Electrolytic reduction"

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Hundley, Gary L. Electrolytic reduction of cobalt in ammoniacal leach solutions. [Avondale, Md.]: U.S. Dept. of the Interior, Bureau of Mines, 1985.

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Hudlicky, Milos. Reductions in organic chemistry. 2nd ed. Washington, DC: American Chemical Society, 1996.

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Hudlický, Miloš. Reductions in organic chemistry. 2nd ed. Washington, D.C: American Chemical Society, 1996.

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Oxidation and reduction in organic synthesis. New York: Oxford University Press, 2000.

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Sanka to kangen 30-kō. Tōkyō-to Shinjuku-ku: Asakura Shoten, 2012.

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Masato, Kitamura, and Nihon Kagakkai, eds. Sanka kangen hannō. Tōkyō-to Bunkyō-ku: Kyōritsu Shuppan, 2012.

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D, McNicol B., ed. Temperature-programmed reduction for solid materials characterization. New York: M. Dekker, 1986.

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Chemical fixation of carbon dioxide: Methods for recycling CO₂ into useful products. Boca Raton: CRC Press, 1993.

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Mahrwald, Rainer. Enantioselective Organocatalyzed Reactions I: Enantioselective Oxidation, Reduction, Functionalization and Desymmetrization. Dordrecht: Springer Science+Business Media B.V., 2011.

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Bruijn, Willem de. The reduction of iron oxides with special reference to the presence of foreign elements: Mineralogical and physical factors influencing reduction behavior. Delft: Delft University Press, 1990.

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Book chapters on the topic "Reduction (Chemistry) Electrolytic reduction"

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Tabereaux, Alton T., Tom R. Alcorn, and Luke Trembley. "Lithium-Modified Low Ratio Electrolyte Chemistry for Improved Performance in Modern Reduction Cells." In Essential Readings in Light Metals, 83–88. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118647851.ch11.

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Tabereaux, Alton T., Tom R. Alcorn, and Luke Trembley. "Lithium-Modified Low Ratio Electrolyte Chemistry for Improved Performance in Modern Reduction Cells." In Essential Readings in Light Metals, 83–88. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-48156-2_11.

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Damjanovic, A., and P. G. Hudson. "By Electrolytic Reduction." In Inorganic Reactions and Methods, 46–49. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145159.ch21.

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Lewis, Rhobert, and Wynne Evans. "Oxidation and Reduction." In Chemistry, 102–19. London: Macmillan Education UK, 2018. http://dx.doi.org/10.1057/978-1-137-61037-9_7.

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Lewis, Rob, and Wynne Evans. "Oxidation and Reduction." In Chemistry, 95–116. London: Macmillan Education UK, 1997. http://dx.doi.org/10.1007/978-1-349-14045-9_7.

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Lewis, Rob, and Wynne Evans. "Oxidation and Reduction." In Chemistry, 100–117. London: Macmillan Education UK, 2011. http://dx.doi.org/10.1007/978-0-230-34492-1_7.

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Baizer, Manuel M., and John P. Petrovich. "Electrolytic Reductive Coupling: Synthetic and Mechanistic Aspects." In Progress in Physical Organic Chemistry, 189–227. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470171868.ch4.

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Murray, James W., Louis A. Codispoti, and Gernot E. Friederich. "Oxidation-Reduction Environments." In Advances in Chemistry, 157–76. Washington, DC: American Chemical Society, 1995. http://dx.doi.org/10.1021/ba-1995-0244.ch007.

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Shamsuddin, Mohammad. "Reduction of Oxides and Reduction Smelting." In Physical Chemistry of Metallurgical Processes, Second Edition, 149–203. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-58069-8_5.

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Albero, Josep, and Hermenegildo García. "Photocatalytic CO2 Reduction." In Green Chemistry and Sustainable Technology, 1–31. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-48719-8_1.

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Conference papers on the topic "Reduction (Chemistry) Electrolytic reduction"

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Hamouda, A. A., and F. S. Evensen. "Possible Mechanism of the Drag Reduction Phenomenon in Light of the Associated Heat Transfer Reduction." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2005. http://dx.doi.org/10.2118/93405-ms.

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Zha, Wei, and Jimi Tjong. "Electrolytic Plasma Discharging Treatment of Cast Iron for Friction Reduction." In WCX World Congress Experience. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2018. http://dx.doi.org/10.4271/2018-01-0834.

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Irshad, Faran, Rizwan, Mishal, Zaffar, and A. Nauman. "Stacked switched capacitor architecture using electrolytic capacitors for size reduction." In 2016 IEEE 7th Power India International Conference (PIICON). IEEE, 2016. http://dx.doi.org/10.1109/poweri.2016.8077185.

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Lu, Tianfeng, Yiguang Ju, and Chung Law. "Complex CSP for chemistry reduction and analysis." In 39th Aerospace Sciences Meeting and Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2001. http://dx.doi.org/10.2514/6.2001-943.

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Hrach, Rudolf, Vera Hrachova, Jean-Claude Legrand, and Anne-Marie Diamy. "Reduction of reaction mechanisms in plasma chemistry." In 2012 IEEE 39th International Conference on Plasma Sciences (ICOPS). IEEE, 2012. http://dx.doi.org/10.1109/plasma.2012.6383279.

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McCool, C. S., D. W. Green, G. P. Willhite, A. K. Shaw, S. Bhattacharya, and A. Singh. "Permeability Reduction by Treatment with KUSP1 Biopolymer Systems." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1997. http://dx.doi.org/10.2118/37298-ms.

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Ganguly, S., G. P. Willhite, D. W. Green, and C. S. McCool. "Effect of Flow Rate on Disproportionate Permeability Reduction." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2003. http://dx.doi.org/10.2118/80205-ms.

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Hamouda, A. A. "Drag Reduction-Performance in Laboratory Compared to Pipelines." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2003. http://dx.doi.org/10.2118/80258-ms.

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Dominguez, Jesus, Sophie Poizeau, and Laurent Sibille. "Modeling Joule Heating Effect on Lunar Oxygen Generation via Electrolytic Reduction." In 47th AIAA Aerospace Sciences Meeting including The New Horizons Forum and Aerospace Exposition. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2009. http://dx.doi.org/10.2514/6.2009-1388.

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Gdanski, Rick David. "Modeling the Impact of Capillary Pressure Reduction by Surfactants." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2007. http://dx.doi.org/10.2118/106062-ms.

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Reports on the topic "Reduction (Chemistry) Electrolytic reduction"

1

Jackson, Jay Matthew, Marisa Jennifer Monreal, Kirk Ryan Weisbrod, David Anthony Tyler Rodriguez, and Michael F. Simpson. Electrolytic Oxide Reduction of Plutonium Oxide Surrogates. Office of Scientific and Technical Information (OSTI), October 2018. http://dx.doi.org/10.2172/1475332.

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2

Staun, Selena Lee, and Andrew James Gaunt. Neptunium and Uranium Reduction Chemistry. Office of Scientific and Technical Information (OSTI), June 2020. http://dx.doi.org/10.2172/1635506.

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3

Staun, Selena Lee, and Andrew James Gaunt. Neptunium and Uranium Reduction Chemistry-A. Office of Scientific and Technical Information (OSTI), March 2020. http://dx.doi.org/10.2172/1606335.

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4

Frank, Robert A. Physical chemistry of carbothermic reduction of alumina. Office of Scientific and Technical Information (OSTI), September 1985. http://dx.doi.org/10.2172/6570345.

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5

Brown, J. R. Surface chemistry and reduction behaviour of y-alumina supported molybdenum oxide. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1987. http://dx.doi.org/10.4095/304349.

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6

Hovey, Megan. Ligand strategies for green chemistry. Catalysts for amide reduction and hydroamination. Office of Scientific and Technical Information (OSTI), January 2014. http://dx.doi.org/10.2172/1226561.

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7

Hiremath, Varun, Steven R. Lantz, Haifeng Wang, and Stephen B. Pope. Large-Scale Parallel Simulations of Turbulent Combustion using Combined Dimension Reduction and Tabulation of Chemistry. Fort Belvoir, VA: Defense Technical Information Center, May 2012. http://dx.doi.org/10.21236/ada569795.

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8

Gopalan, Srikanth. Solid Oxide Fuel Cell Cathodes. Unraveling the Relationship Between Structure, Surface Chemistry and Oxygen Reduction. Office of Scientific and Technical Information (OSTI), March 2013. http://dx.doi.org/10.2172/1214271.

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9

Blake, D. M., E. Wolfrum, and J. Boulter. Photocatalytic oxidation and reduction chemistry and a new process for treatment of pink water and related contaminated water. Office of Scientific and Technical Information (OSTI), October 1996. http://dx.doi.org/10.2172/395626.

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