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Artículos de revistas sobre el tema "Oxidation reduction"

Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 25 de julio de 2025

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1

Nam, K. W., H. R. Jeong, and S. H. Ahn. "VOCs Removal by Oxidation/Reduction Reaction of Cu-Doped Photocatalyst." International Journal of Chemical Engineering and Applications 7, no. 6 (2016): 359–64. http://dx.doi.org/10.18178/ijcea.2016.7.6.605.

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2

Nan Yao and Yu Lin Hu, Nan Yao and Yu Lin Hu. "Recent Progress in the Application of Ionic Liquids in Electrochemical Oxidation and Reduction." Journal of the chemical society of pakistan 41, no. 2 (2019): 264. http://dx.doi.org/10.52568/000728/jcsp/41.02.2019.

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Electrochemical oxidation and reduction, with clean power, are key to energy conversion and storage. For example, electrochemical oxidation is a determining step for fuel cells, combination of electrochemical oxidation and reduction can form a metal-air battery. Electrochemical oxidation and reduction make significant contributions to prepare valuable chemicals directly and improve yield efficiency and reduce the three wastes, which have become one of the green methodologies. Ionic liquids have attracted increasing attentions in the area of electrochemistry due to their significant properties

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3

Hertz, Leif. "Brain Glutamine Synthesis Requires Neuronal Aspartate: A Commentary." Journal of Cerebral Blood Flow & Metabolism 31, no. 1 (2010): 384–87. http://dx.doi.org/10.1038/jcbfm.2010.199.

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Inspired by the paper, ‘Brain glutamine synthesis requires neuronal-born aspartate as amino donor for glial glutamate formation’ by Pardo et al, a modified model of oxidation–reduction, transamination, and mitochondrial carrier reactions involved in aspartate-dependent astrocytic glutamine synthesis and oxidation is proposed. The alternative model retains the need for cytosolic aspartate for transamination of α-ketoglutarate, but the ‘missing’ aspartate molecule is generated within astrocytes during subsequent glutamate oxidation. Oxaloacetate formed during glutamate formation is used during g

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4

Cerciello, Francesca, Antonio Fabozzi, Christoph Yannakis, et al. "Kinetics of iron reduction upon reduction/oxidation cycles." International Journal of Hydrogen Energy 65 (May 2024): 337–47. http://dx.doi.org/10.1016/j.ijhydene.2024.04.008.

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5

Emerenciano, Vicente P., D. Cabrol-Bass, Marcelo J. P. Ferreira, et al. "Chemical Evolution in the Asteraceae. The Oxidation– Reduction Mechanism and Production of Secondary Metabolites." Natural Product Communications 1, no. 6 (2006): 1934578X0600100. http://dx.doi.org/10.1177/1934578x0600100612.

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This work describes the application of partial least squares (PLS) regression to variables that represent the oxidation data of several types of secondary metabolite isolated from the family Asteraceae. The oxidation states were calculated for each carbon atom of the involved compounds after these had been matched with their biogenetic precursor. The states of oxidation variations were named oxidation steps. This methodology represents a new approach to inspect the oxidative changes in taxa. Partial least square (PLS) regression was used to inspect the relationships among terpenoids, coumarins

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6

HIROHASHI, Ryo. "Oxidation-Reduction of Organic Dyes." Journal of the Japan Society of Colour Material 64, no. 2 (1991): 92–99. http://dx.doi.org/10.4011/shikizai1937.64.92.

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7

Khandelwal, Y., G. Moraes, N. J. de Souza, H. W. Fehihaber, and E. F. Paulus. "Oxidation/reduction studies with forskolin." Tetrahedron Letters 27, no. 51 (1986): 6249–52. http://dx.doi.org/10.1016/s0040-4039(00)85444-1.

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8

Millis, Kevin K., Kim H. Weaver, and Dallas L. Rabenstein. "Oxidation/reduction potential of glutathione." Journal of Organic Chemistry 58, no. 15 (1993): 4144–46. http://dx.doi.org/10.1021/jo00067a060.

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9

Schrittwieser, Joerg H., Johann Sattler, Verena Resch, Francesco G. Mutti, and Wolfgang Kroutil. "Recent biocatalytic oxidation–reduction cascades." Current Opinion in Chemical Biology 15, no. 2 (2011): 249–56. http://dx.doi.org/10.1016/j.cbpa.2010.11.010.

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10

Schink, Bernhard, and Michael Friedrich. "Phosphite oxidation by sulphate reduction." Nature 406, no. 6791 (2000): 37. http://dx.doi.org/10.1038/35017644.

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11

Davis, B. G. "ChemInform Abstract: Oxidation and Reduction." ChemInform 31, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.200017252.

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12

FLEET, G. W. J. "ChemInform Abstract: Oxidation and Reduction." ChemInform 26, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199536309.

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13

Davis, B. G., and J. A. G. Williams. "ChemInform Abstract: Oxidation and Reduction." ChemInform 33, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.200250270.

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14

FLEET, G. W. J. "ChemInform Abstract: Oxidation and Reduction." ChemInform 28, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.199730262.

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15

Banerji, K. K. "ChemInform Abstract: Oxidation and Reduction." ChemInform 44, no. 33 (2013): no. http://dx.doi.org/10.1002/chin.201333243.

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16

Mehrotra, R. N. "ChemInform Abstract: Oxidation and Reduction." ChemInform 42, no. 46 (2011): no. http://dx.doi.org/10.1002/chin.201146254.

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17

FLEET, G. W. J. "ChemInform Abstract: Oxidation and Reduction." ChemInform 24, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199302301.

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18

Elema, B. "Oxidation-reduction potentials of chlororaphine." Recueil des Travaux Chimiques des Pays-Bas 52, no. 7 (2010): 569–83. http://dx.doi.org/10.1002/recl.19330520706.

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19

Wang, Liang, and Feng-Shou Xiao. "Methane oxidation by catalyst reduction." Nature Catalysis 6, no. 10 (2023): 866–67. http://dx.doi.org/10.1038/s41929-023-01044-w.

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20

Biswas, Salah Uddin, Kripasindhu Karmakar, and Bidyut Saha. "Oxidation‐reduction reactions in geochemistry." Vietnam Journal of Chemistry 59, no. 2 (2021): 133–45. http://dx.doi.org/10.1002/vjch.202000196.

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AbstractThere are more than hundred elements in the periodic table and many of them are associated with various geochemical processes. Most of the elements can show more than one oxidation states, therefore, reactions involving oxidation and reduction are of very much importance in geochemistry. Since every change (chemical or physical) is associated with the change of energy, hence for every single process, there should be a reliable way for quantitative measurement of energy change. In case of any redox process, the energy change can be quantitatively expressed in terms of reduction potentia

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21

Paul, Amal. "Oxidation-reduction equilibrium in glass." Journal of Non-Crystalline Solids 123, no. 1-3 (1990): 354–62. http://dx.doi.org/10.1016/0022-3093(90)90808-y.

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22

FLEET, G. W. J. "ChemInform Abstract: Oxidation and Reduction." ChemInform 22, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199132283.

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23

Martín-Martín, Juan Alberto, Asier Aranzabal, María Pilar González-Marcos, Elisabetta Finocchio, and Juan Ramón González-Velasco. "Reaction mechanism of 1,2-dichlorobenzene oxidation over MnOX-CeO2 and the effect of simultaneous NO selective reduction." Chemical Engineering Journal 498 (September 7, 2024): 155570. https://doi.org/10.1016/j.cej.2024.155570.

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[ABSTRACT] MnO<sub>X</sub>-CeO<sub>2</sub> formulation has been studied for the catalytic oxidation of 1,2-dichlorobenzene. Among the samples with different Mn and Ce content, the most active was 85%mol Mn and 15%mol Ce, due to its better morphological properties and the synergy achieved between the two phases composing it (mixed oxide phase and segregated Mn oxide). Deactivation was monitored at low temperature and a transient change in the oxidative capability at high temperature because of active sites with different oxidative capability. Based on in-situ FTIR results, oxidation reaction pa

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24

Tapalova, A., and O. Suleimenova. "Electrochemical analysis of oxidation-reduction reactions." Chemical Bulletin of Kazakh National University, no. 1 (May 14, 2013): 148. http://dx.doi.org/10.15328/chemb_2013_1148-154.

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25

Carter, Dean E. "Oxidation-Reduction Reactions of Metal Ions." Environmental Health Perspectives 103 (February 1995): 17. http://dx.doi.org/10.2307/3432005.

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26

Carter, D. E. "Oxidation-reduction reactions of metal ions." Environmental Health Perspectives 103, suppl 1 (1995): 17–19. http://dx.doi.org/10.1289/ehp.95103s117.

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27

Lovley, D. R., J. D. Coates, J. C. Woodward, and E. Phillips. "Benzene oxidation coupled to sulfate reduction." Applied and environmental microbiology 61, no. 3 (1995): 953–58. http://dx.doi.org/10.1128/aem.61.3.953-958.1995.

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28

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 (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 o

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29

Raber, Douglas J., and Walter Rodriguez. "Conformational properties of oxidation-reduction cofactors." Journal of the American Chemical Society 107, no. 14 (1985): 4146–47. http://dx.doi.org/10.1021/ja00300a009.

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30

Anselme, Jean-Pierre. "Understanding Oxidation - Reduction in Organic Chemistry." Journal of Chemical Education 74, no. 1 (1997): 69. http://dx.doi.org/10.1021/ed074p69.

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31

Pace, Charles, and Marian Stankovich. "Oxidation-reduction properties of glycolate oxidase." Biochemistry 25, no. 9 (1986): 2516–22. http://dx.doi.org/10.1021/bi00357a035.

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32

Barcelona, Michael J., and Thomas R. Holm. "Oxidation-reduction capacities of aquifer solids." Environmental Science & Technology 25, no. 9 (1991): 1565–72. http://dx.doi.org/10.1021/es00021a006.

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33

Silverstein, Todd P. "Oxidation and Reduction: Too Many Definitions?" Journal of Chemical Education 88, no. 3 (2011): 279–81. http://dx.doi.org/10.1021/ed100777q.

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34

Kim, Geumsoo, Stephen J. Weiss, and Rodney L. Levine. "Methionine oxidation and reduction in proteins." Biochimica et Biophysica Acta (BBA) - General Subjects 1840, no. 2 (2014): 901–5. http://dx.doi.org/10.1016/j.bbagen.2013.04.038.

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35

Davies, Peter K., та Cynthia M. Katzan. "Oxidation and reduction of BaLa4Cu5O13+δ". Journal of Solid State Chemistry 88, № 2 (1990): 368–83. http://dx.doi.org/10.1016/0022-4596(90)90231-l.

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36

Readey, Dennis W. "Oxidation and Reduction of Ceramic Composites." Materials Science Forum 251-254 (October 1997): 861–68. http://dx.doi.org/10.4028/www.scientific.net/msf.251-254.861.

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37

Hong, Yi-Zhe, Wei-Huan Chiang, Hung-Chieh Tsai, et al. "Local oxidation and reduction of graphene." Nanotechnology 28, no. 39 (2017): 395704. http://dx.doi.org/10.1088/1361-6528/aa802d.

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38

Coombs, P. G., and Z. A. Munir. "Cyclic reduction-oxidation of haematite powders." Journal of Materials Science 24, no. 11 (1989): 3913–23. http://dx.doi.org/10.1007/bf01168954.

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39

Rahman, Md Abdur, David R. Kelly, Prasad Ravi, Russell Underwood, and Bert Fraser-Reid. "Controlled reduction and oxidation of actinobolin." Tetrahedron 42, no. 9 (1986): 2409–16. http://dx.doi.org/10.1016/0040-4020(86)80003-5.

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40

Swarts, Pieter J., and Jeanet Conradie. "Oxidation and reduction data of subphthalocyanines." Data in Brief 28 (February 2020): 105039. http://dx.doi.org/10.1016/j.dib.2019.105039.

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41

Becker, James Y. "Electrochemical Oxidation and Reduction of Allenes." Israel Journal of Chemistry 26, no. 2 (1985): 196–206. http://dx.doi.org/10.1002/ijch.198500093.

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42

Yang, Chia-Hsi, and You-Chung Lin. "The Self Oxidation Reduction ofN-Arylhydroxylamines." Journal of the Chinese Chemical Society 34, no. 1 (1987): 19–24. http://dx.doi.org/10.1002/jccs.198700004.

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43

Jellinek, Max. "Oxidation-Reduction Maintenance in Organ Preservation." Archives of Surgery 120, no. 4 (1985): 439. http://dx.doi.org/10.1001/archsurg.1985.01390280033008.

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44

Yeow, Jonathan, Amandeep Kaur, Matthew D. Anscomb, and Elizabeth J. New. "A novel flavin derivative reveals the impact of glucose on oxidative stress in adipocytes." Chem. Commun. 50, no. 60 (2014): 8181–84. http://dx.doi.org/10.1039/c4cc03464c.

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45

Wang, Tao, Yan Hong Leng, and Lian Sheng Chen. "The Study on High-Temperature Oxidation Law of 20CrMo Steel in the Regenerative Heating Furnace." Advanced Materials Research 291-294 (July 2011): 778–81. http://dx.doi.org/10.4028/www.scientific.net/amr.291-294.778.

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The special atmosphere of oxidation and reduction combustion in regenerative heating furnace is confirmed by anglicizing working principle of the furnace, and the growth and nature of steel’s oxide layer is influenced by the special combustion atmosphere. From the respects of thermodynamics and kinetics, the high-temperature oxidation regular of 20CrMo steel is studied. The oxidative production include steady oxide of Fe2O3、Fe3O4、FeO.The oxide layer grow slowly when temperature below 1100°C, but speedily when it is over1100°C. With the commutation of valve, the combustion atmosphere of regener

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46

Jung, S.-C., and W.-S. Yoon. "Modelling and parametric investigation of NOx reduction by oxidation precatalyst-assisted ammonia-selective catalytic reduction." Proceedings of the Institution of Mechanical Engineers, Part D: Journal of Automobile Engineering 223, no. 9 (2009): 1193–206. http://dx.doi.org/10.1243/09544070jauto1099.

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Nitrogen oxide (NO x) reduction by the selective catalytic reduction (SCR) system assisted by an oxidation precatalyst is modelled and analytically investigated. The Langmuir—Hinshelwood SCR kinetic scheme with vanadium-based catalyst and ammonia (NH3) reductant in conjunction with the NO—NO2 conversion reaction over a platinum-based catalyst is used. The effects of the ratio of the oxidation precatalyst to the SCR monolith volume, the gas temperature, the space velocity, and the NH3-to-NO x concentration ratio on the de-NO x performance are parametrically examined. The oxidation precatalyst p

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47

B., Sethuram. "Electron transfer reactions involving organic molecules." Journal of Indian Chemical Society Vol. 78, Apr 2001 (2001): 159–74. https://doi.org/10.5281/zenodo.5849779.

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48

Sadasivan, Sajanikumari, Ronan M. Bellabarba, and Robert P. Tooze. "Size dependent reduction–oxidation–reduction behaviour of cobalt oxide nanocrystals." Nanoscale 5, no. 22 (2013): 11139. http://dx.doi.org/10.1039/c3nr02877a.

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49

Goodby, Brian E., and Jeanne E. Pemberton. "XPS Characterization of a Commercial Cu/ZnO/Al2O3 Catalyst: Effects of Oxidation, Reduction, and the Steam Reformation of Methanol." Applied Spectroscopy 42, no. 5 (1988): 754–60. http://dx.doi.org/10.1366/0003702884429148.

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X-ray photoelectron spectroscopy (XPS) is used to characterize the surface region of a commercial Cu/ZnO/Al2O3 (33/66/1 wt %) catalyst. A systematic study of the effects of oxidation, reduction, and the steam reformation of methanol on the oxidative state of the Cu component is presented. The Zn XPS features show no changes due to the various treatments. Peak fitting procedures were developed to quantitate the Cu oxidation states on the basis of the XPS Cu 2P3/2 main and satellite features. After oxidation in pure O2 at 300°C, all Cu exists as Cu+2. The Cu/Zn ratio changes from 0.28 to 0.37 as

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50

Mishchenko, Denis D., Zakhar S. Vinokurov, Tatyana N. Afonasenko та ін. "Insights into the Contribution of Oxidation-Reduction Pretreatment for Mn0.2Zr0.8O2−δ Catalyst of CO Oxidation Reaction". Materials 16, № 9 (2023): 3508. http://dx.doi.org/10.3390/ma16093508.

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A Mn0.2Zr0.8O2−δ mixed oxide catalyst was synthesized via the co-precipitation method and studied in a CO oxidation reaction after different redox pretreatments. The surface and structural properties of the catalyst were studied before and after the pretreatment using XRD, XANES, XPS, and TEM techniques. Operando XRD was used to monitor the changes in the crystal structure under pretreatment and reaction conditions. The catalytic properties were found to depend on the activation procedure: reducing the CO atmosphere at 400–600 °C and the reaction mixture (O2 excess) or oxidative O2 atmosphere

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