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Relevant bibliographies by topics / Oxidation Transition metal halides

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Academic literature on the topic 'Oxidation Transition metal halides'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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Journal articles on the topic "Oxidation Transition metal halides"

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Yadav, Sangeeta, Sudesh T. Manjare, Harkesh B. Singh, and Ray J. Butcher. "Transition metal mediated formation of dicationic diselenides stabilised by N-heterocyclic carbenes: designed synthesis." Dalton Transactions 45, no. 30 (2016): 12015–27. http://dx.doi.org/10.1039/c6dt01425a.

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Rossi, Laura, and A´ngela Sua´rez. "Transition metal halides as catalysts in the oxidation reaction of sulfides into sulfoxides." Sulfur Letters 25, no. 3 (January 2002): 123–27. http://dx.doi.org/10.1080/02786110212863.

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Swarnakar, Anindya K., Michael J. Ferguson, Robert McDonald, and Eric Rivard. "Transition metal-mediated donor–acceptor coordination of low-oxidation state Group 14 element halides." Dalton Transactions 45, no. 14 (2016): 6071–78. http://dx.doi.org/10.1039/c5dt03018h.

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Wang, Ying, Yang Wang, Kai Jiang, Qian Zhang, and Dong Li. "Transition-metal-free oxidative C5 C–H-halogenation of 8-aminoquinoline amides using sodium halides." Organic & Biomolecular Chemistry 14, no. 43 (2016): 10180–84. http://dx.doi.org/10.1039/c6ob02079h.

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Bortoluzzi, Marco, Eleonora Ferretti, Fabio Marchetti, Guido Pampaloni, and Stefano Zacchini. "A structurally-characterized NbCl5–NHC adduct." Chem. Commun. 50, no. 34 (2014): 4472–74. http://dx.doi.org/10.1039/c4cc01575d.

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Sellmann, Dieter, Gerhard Freyberger, and Matthias Moll. "Übergangsmetallkomplexe mit Schwefelliganden, XLVIa. Zn-, Cd-, Hg-, Sn-, Pb-, Sb-, Bi- und Ti-Komplexe mit den zwei- und vierzähnigen Thiolatliganden 'buS2'2- = 3,5-Di(t-butyl)benzol-1,2-dithiolat(2—), 'S4'2- = 1,2-Bis(2-mercaptophenylthio)ethan(2—) und 'buS4'2- = 1,2-Bis(3,5-di(t-butyl)-2-mercaptophenylthio)ethan(2–) / Transition Metal Complexes with Sulfur Ligands, XLVIa. Zn, Cd, Hg, Sn, Pb, Bi and Ti Complexes with the Bi- and Tetradentate Thiolato Ligands 'buS2'2- = 3,5-Di(t-butyl)benzene-1,2-dithiolate(2–), 'S4'2 = 1,2-Bis(2-mercaptophenylthio)ethane(2–) and 'buS4'2- = 1,2-Bis(3,5-di(t-butyl)-2-mercaptophenylthio)ethane(2 – )." Zeitschrift für Naturforschung B 44, no. 9 (September 1, 1989): 1015–22. http://dx.doi.org/10.1515/znb-1989-0905.

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Syntheses of neutral 'buS2'-, 'S4'- and 'buS4'- and of anionic .buS2-complexes with various main group and transition metals are described. The complexes were prepared by reacting the neutral sulfur ligands or their alkali salts with the metal halide or alkoxide. The ligands coordinate to metal ions in normal as well as high oxidation states. No redox reactions occur in the latter case. The complexes are usually soluble in organic solvents and were characterized by elemental analysis and spectroscopic means.

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Anuma, Saroja, and Badekai Ramachandra Bhat. "Nanographene Sheet Immobilized Transition Metal Complexes for C-C Coupling Reactions." International Journal of Engineering & Technology 7, no. 4.5 (September 22, 2018): 431. http://dx.doi.org/10.14419/ijet.v7i4.5.20199.

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Transition metal Schiff base complexes covalently immobilized on the surface of amino functionalized graphene sheet to catalyze C-C coupling reaction is reported. Graphene sheet which synthesized using mechanical exfoliation and then by differential oxidative reduction phenomenon of graphite. The schiff base ligand is prepared using aldehyde and amino groups containing compounds which further treated with metal salts to form metal complexes. The as-synthesized metal complexes was then incorporated into amino functionalized nanosheets which are characterized using different spectrochemical techniques. The catalytic investigation of the as-prepared catalyst were done by the cross coupling of aryl halides and aryl boronic acids to form biaryls as product in C-C cross coupling reaction. The yield of the products were high and selective which were analyzed using Gas chromatography technique. The advantage of this catalyst is high stability, recyclability easy recovery of catalyst, environmentally benign and mild reaction condition.

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Malisch, Wolfgang, Katharina Thirase, and Joachim Reising. "Ubergangsmetall-substituierte Phosphane, Arsane und Stibane, LX [1]. Ferrio-(thiocarbamoyl)phosphane Cp(OC)2 Fe-P(Mes)[C(=S)-N(R)H] (R = Me, Et, f-Bu): Aufbau aus dem Ferrio-mesitylphosphan Cp(OC)2 Fe-P(Mes)H und Organoisothiocyanaten sowie Quaternisierung mit Alkylhalogeniden und Oxidation mit Schwefel / Transition Metal Substituted Phosphanes, Arsanes and Stibanes, LX [1]. Ferrio-(thiocarbamoyl)phosphanes Cp(OC)2Fe-P(Mes)[C(=S)-N(R)H] (R= Me, Et, r-Bu): Build-up from the Ferrio-mesitylphosphane Cp(OC)2Fe-P(Mes)H and Organoisothiocyanates, Quatemization with Alkyl Halides and Oxidation with Sulfur." Zeitschrift für Naturforschung B 53, no. 10 (October 1, 1998): 1084–91. http://dx.doi.org/10.1515/znb-1998-1002.

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AbstractArsane und Stibane, LX [1]. Ferrio-(thiocarbamoyl)phosphane Cp(OC)2Fe-P(Mes)[C(=S)-N(R)H] (R = Me, Et, f-Bu): Aufbau aus dem Ferrio-mesitylphosphan Cp(OC)2Fe-P(Mes)H und Organoisothiocyanaten sowie Quaternisierung mit Alkylhalogeniden und Oxidation mit Schwefel Transition Metal Substituted Phosphanes, Arsanes and Stibanes, LX [1]. Ferrio-(thiocarbamoyl)phosphanes Cp(OC)2Fe-P(Mes)[C(=S)-N(R)H] (R= Me, Et, r-Bu): Build-up from the Ferrio-mesitylphosphane Cp(OC)2Fe-P(Mes)H and Organoisothiocyanates, Quatemization with Alkyl Halides and Oxidation with Sulfur The ferrio-phosphane Cp(OC)2Fe-P(Mes)H (4), obtained by deprotonation of the me-sitylphosphane iron complex {Cp(OC)2 [H2(Mes)P]Fe}BF4 (3), reacts with the organoiso thiocyanates RNCS (R = Me, Et, Ph) (5a -c) to give the functionalized ferrio-phosphanes Cp(OC)2Fe-P(Mes)[C(=S)-N(R)H] (6a-c). Quatemization of 6a,b at the phosphorus atom with the alkyl halides R′-Hal (R1 = Me, Et, CH2 Ph) (7a-c) yields the complexes {Cp(OC)2Fe-P(Mes)(R′)[C(=S)-N(H)(R)]}Hal (8a-d), whereas oxidation with elemental sulfur affords the ferrio-thiophosphoranes Cp(OC)2Fe-P(=S)(Mes)[C(=S)-N(R)H] (R = Me, Et) (10a,b). 10b is alkylated with Mel to give {Cp(OC)2Fe-P(SMe)(Mes)[C(=S)-N(Et)H]}I (11). The structure of 8b has been determined by X-ray analysis.

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Welin, Eric R., Chip Le, Daniela M. Arias-Rotondo, James K. McCusker, and David W. C. MacMillan. "Photosensitized, energy transfer-mediated organometallic catalysis through electronically excited nickel(II)." Science 355, no. 6323 (January 26, 2017): 380–85. http://dx.doi.org/10.1126/science.aal2490.

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Transition metal catalysis has traditionally relied on organometallic complexes that can cycle through a series of ground-state oxidation levels to achieve a series of discrete yet fundamental fragment-coupling steps. The viability of excited-state organometallic catalysis via direct photoexcitation has been demonstrated. Although the utility of triplet sensitization by energy transfer has long been known as a powerful activation mode in organic photochemistry, it is surprising to recognize that photosensitization mechanisms to access excited-state organometallic catalysts have lagged far behind. Here, we demonstrate excited-state organometallic catalysis via such an activation pathway: Energy transfer from an iridium sensitizer produces an excited-state nickel complex that couples aryl halides with carboxylic acids. Detailed mechanistic studies confirm the role of photosensitization via energy transfer.

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Beck, Johannes, and Joerg Wetterau. "Chalcogen Polycations by Oxidation of Elemental Chalcogens with Transition Metal Halides: Synthesis and Crystal Structure of [Se17][WCl6]2." Inorganic Chemistry 34, no. 24 (November 1995): 6202–4. http://dx.doi.org/10.1021/ic00128a036.

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Dissertations / Theses on the topic "Oxidation Transition metal halides"

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Moock, K. H. "Electrochemical studies on transition metal halides." Thesis, University of Glasgow, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375467.

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Field, Marianne Alice Louise. "Transition metal oxides and oxide-halides." Thesis, University of Southampton, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.401833.

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Ye, Jianjun. "Electronic spectroscopy of transition metal monohalides." Click to view the E-thesis via HKUTO, 2007. http://sunzi.lib.hku.hk/hkuto/record/B38990167.

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Hodges, Philip J. "Transition metal halides, studied by high-resolution electronic spectroscopy." Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433477.

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Rispens, Minze Theunis. "Enantioselective oxidation using transition metal catalysts." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 1996. http://irs.ub.rug.nl/ppn/291237975.

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Orrin, Rachel H. "Photo-oxidation of transition metal carbonyls." Thesis, University of Reading, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317044.

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Opre, Zsuzsanna. "Catalytic oxidation over transition metal containing hydroxyapatites /." Zürich : ETH, 2007. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=17247.

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Handley, Darren. "Triangulo-trinuclear tmeda complexes of the first transition series." Thesis, University of Sussex, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311347.

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Wilson, Antony. "A matrix isolation study of transition metal halides and their structure." Thesis, University of Hull, 2009. http://hydra.hull.ac.uk/resources/hull:2527.

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The work within this thesis has concentrated on the formation and isolation of titanium, vanadium, palladium, and mercury halides, with emphasis on the fluorides.TiF, TiF2, TiF3, and TiF4 have all been isolated within an argon matrix and infrared spectra obtained. From the titanium isotope splitting pattern a bond angle has been determined for TiF2 for the first time of 165o, or effectively linear. This work is also the first time that TiF has been isolated within an argon matrix. Work has also been conducted with vanadium which has lead to the isolation of VF5, VF4, VF3, and VF2, with VF4 undergoing Fermi Resonance. This is the first time that VF4 and VF2, consistent with a linear structure, have been isolated within a matrix.Work conducted upon palladium led to the isolation of numerous palladium fluorides, identified by the palladium isotope patterns in their IR spectra. Due to the similarity of the calculated stretching frequencies of PdF2, PdF3, PdF4, and PdF6 the assignment was challenging and so identification of these bands was conducted based photolysis and annealing behaviour in conjunction with computational calculations. This has allowed for the assignment of the bands present to PdF6, PdF4, PdF3, PdF2, and PdF.The bond length of molecular HgF2 has also been determined for the first time at 1.94(2) Å using the Hg L3-edge with EXAFS. Although the initial aim of this work was to isolate HgF4, using IR, UV/Vis, and XANES, no evidence could be found for oxidation states of mercury higher that HgII. The work also developed a new clean way of making HgF2 in a matrix. The identification of a new Hg…X2 complex was also discovered which when photolysed forms the HgX2 compound, this has only been proven for HgF2. This was achieved by isolating mercury atoms in an argon matrix doped matrices, photolysis of this matrix the led to the formation of HgF2 in significant amounts.

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Spittle, Peta Jean. "Characterisation of high temperature metal halides by mass spectrometry and matrix isolation infrared spectroscopy." Thesis, University of Southampton, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242391.

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Books on the topic "Oxidation Transition metal halides"

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Cardona, Francesca, and Camilla Parmeggiani, eds. Transition Metal Catalysis in Aerobic Alcohol Oxidation. Cambridge: Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/9781782621652.

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Goldmann, A., ed. Noble Metals, Noble Metal Halides and Nonmagnetic Transition Metals. Berlin/Heidelberg: Springer-Verlag, 2003. http://dx.doi.org/10.1007/b72681.

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Henderson, Richard A. The mechanisms of reactions at transition metal sites. Oxford: Oxford University Press, 1997.

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Ravindran, Mythili. Synthesis and structural studies of N - and O - donor complexes of transition and post-transition metal halides. [s.l.]: typescript, 1991.

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Lakin, Miles T. Complexation of early- and post- transition metal halides with aza-, oxa-, and thiamacrocyclic ligands. [s.l.]: typescript, 1993.

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Lange, Norbert. Schwingungsspektroskopische Untersuchungen an Erdalkali- und Übergangsmetallhalogenaten. Rheinfelden: Schäuble, 1992.

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Cavani, Fabrizio, Camilla Parmeggiani, Teruyuki Kondo, Tapan Kanti Paine, and Masayuki Kirihara. Transition Metal Catalysis in Aerobic Alcohol Oxidation. Royal Society of Chemistry, The, 2014.

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Goldmann, A. Noble Metals, Noble Metal Halides and Nonmagnetic Transition Metals. Springer, 2003.

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9

Biomimetic Oxidations Catalyzed by Transition Metal Complexes. World Scientific Publishing Company, 2000.

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10

Lo, Kenneth. Catalytic oxidation of organic substrates using transition metal complexes. 1997.

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Book chapters on the topic "Oxidation Transition metal halides"

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Page, E. M. "Of Transition-Metal Halides by Oxidative Addition by Alkyl Halides." In Inorganic Reactions and Methods, 185. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145180.ch113.

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Röschenthaler, G. V. "Of Transition-Metal Halides." In Inorganic Reactions and Methods, 220. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145173.ch153.

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Page, E. M. "Of Transition-Metal Halides by Halogenation with Non-Transition-Metal Halides." In Inorganic Reactions and Methods, 181–82. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145180.ch111.

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Page, E. M. "Of Transition-Metal Halides Electrochemically." In Inorganic Reactions and Methods, 182–84. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145180.ch112.

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Brandsma, L., H. D. Verkruijsse, and S. F. Vasilevsky. "Copper(I)-Halide-Catalyzed Oxidative Coupling of Acetylenes." In Application of Transition Metal Catalysts in Organic Synthesis, 67–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-60328-0_5.

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Page, E. M., and D. A. Rice. "From Transition-Metal Halides with Chalcogens." In Inorganic Reactions and Methods, 240–42. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145180.ch157.

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Adolfsson, Hans. "Transition Metal-Catalyzed Epoxidation of Alkenes." In Modern Oxidation Methods, 21–49. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603689.ch2.

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Adolfsson, Hans. "Transition Metal-Catalyzed Epoxidation of Alkenes." In Modern Oxidation Methods, 37–84. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632039.ch2.

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Röschenthaler, G. V. "To Give Group-VB Halides from Transition-Metal Halides." In Inorganic Reactions and Methods, 213. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145173.ch139.

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Dyke, C. H. Van. "By Silver and Other Transition-Metal Halides." In Inorganic Reactions and Methods, 356–58. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145173.ch263.

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Conference papers on the topic "Oxidation Transition metal halides"

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El Hefnawy, Somia M., Mervet M. Aboelkher, and H. Abdelkader. "IR analysis of polyvinylidene fluoride doped with transition metal halides." In SPIE Scanning Microscopy, edited by Michael T. Postek, Dale E. Newbury, S. Frank Platek, and David C. Joy. SPIE, 2009. http://dx.doi.org/10.1117/12.820521.

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El Hefnawy, Somia M., Mervet M. Aboelkher, and H. Abdelkader. "X-ray analysis of polyvinylidene fluoride doped with transition metal halides." In SPIE Scanning Microscopy, edited by Michael T. Postek, Dale E. Newbury, S. Frank Platek, and David C. Joy. SPIE, 2009. http://dx.doi.org/10.1117/12.819433.

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VAN SANTEN, R. A. "SELECTIVE CATALYTIC OXIDATION BY HETEROGENEOUS TRANSITION METAL CATALYSTS." In Proceedings of the NIOK (Netherlands Institute for Catalysis Research) Course on Catalytic Oxidation. WORLD SCIENTIFIC, 1995. http://dx.doi.org/10.1142/9789814503884_0004.

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Jiménez-Mier, J., P. Olalde-Velasco, G. Carabalí-Sandoval, G. Herrera-Pérez, E. Chavira, W. L. Yang, and J. Denlinger. "X-ray absorption to determine the metal oxidation state of transition metal compounds." In RADIATION PHYSICS: IX International Symposium on Radiation Physics. AIP, 2013. http://dx.doi.org/10.1063/1.4813463.

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Zhang, Yu, Jiti Zhou, Chengyu Li, Guodong Wang, and Shiyuan Guo. "Research progress on liquid-phase catalysis of SO2 oxidation by transition metal ions." In 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5965790.

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Zou, Hanbo, Shengzhou Chen, Zili Liu, and Weiming Lin. "Study on the Catalytic Performance of CuO-CeO2 Catalysts Doped with Transition Metal Oxides for Selective CO Oxidation." In 2011 International Conference on Intelligent Computation Technology and Automation (ICICTA). IEEE, 2011. http://dx.doi.org/10.1109/icicta.2011.507.

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Jiménez-Mier, J., P. Olalde-Velasco, W. L. Yang, and J. Denlinger. "Transition metal atomic multiplets in the ligand K-edge x-ray absorption spectra and multiple oxidation states in the L2,3 emission of strongly correlated compounds." In 1ST WORKSHOP ON SPECIALITY OPTICAL FIBERS AND THEIR APPLICATIONS. American Institute of Physics, 2014. http://dx.doi.org/10.1063/1.4890701.

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Fukumoto, M., E. Nishioka, and T. Matsubara. "Effect of Interface Wetting on Flattening of Freely Fallen Metal Droplet Onto Flat Substrate Surface." In ITSC 2000, edited by Christopher C. Berndt. ASM International, 2000. http://dx.doi.org/10.31399/asm.cp.itsc2000p0797.

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Abstract A free falling experiment was conducted as a simulation of a thermal spray process. A flattening behavior of the freely fallen metal droplet impinged onto a flat substrate surface was fundamentally investigated. The substrates were kept at various designated temperatures, and the substrates coated with gold by PVD were also prepared in order to investigate the effect of a wetting at the splat/substrate interface on the flattening behavior of the droplet. A falling atmosphere was atmospheric pressure nitrogen to prevent the oxidation of the melted droplet, and the experiments under low-pressure condition were also conducted. A transition of the splat morphology was recognized in atmospheric pressure nitrogen experiments, that is, the splat morphology on a room temperature substrate was a splash type, whereas that on a high temperature substrate was a disk type. The cross-section microstructure of the splat obtained on the room temperature substrate was an isotropic coarse grain, whereas that on the high temperature substrate was a fine columnar. The grain size changed transitionally with increasing the substrate temperature. Transition temperature on the gold-coated substrate was higher than that on the substrate without coating. The cross-section microstructure of the splat obtained under low-pressure was a fine columnar even on the room temperature substrate. The results indicate that the metal droplet wets better under low-pressure condition than in atmospheric pressure nitrogen condition, and the wetting has a significant role in the flattening of the droplet.

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Vahedi, Nasser, and Alparslan Oztekin. "Experimental Analysis of Kinetics and Cyclic Performance of Cobalt Oxide Powder As Redox Reactant Agent for High-Temperature Thermochemical Energy Storage." In ASME 2019 Heat Transfer Summer Conference collocated with the ASME 2019 13th International Conference on Energy Sustainability. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/ht2019-3681.

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Abstract For continuous operation of Concentrated Solar Power (CSP) Plants it is necessary to integrate thermal energy storage module. High-density energy storage system at a high temperature is required for the new generation of large scale CSP plants. The Thermochemical Energy Storage (TCES) systems use the enthalpy of formation of a reversible chemical reaction for energy storage and release. Gas/solid reduction-oxidation (redox) reactions of solid metal oxides using air as heat transfer fluid (HTF) can be directly integrated with air operated CSP plants, and there is no need for HTF storage and any intermediate heat exchanger. A new generation of large scale CSP plants uses high-temperature solar collectors to increase power cycle efficiency. Such operating conditions require the development of suitable high-temperature TCES systems. The selection of suitable metal oxide reactant is very critical in the design of such high-temperature storage systems and requires a detailed study of the physics of reaction within the reactor. Cobalt oxide (Co3O4/CoO) has been verified to have a high reaction temperature, high enthalpy of reaction together with reasonable cyclic and thermal stability. Unique features of cobalt oxide require more fundamental study of the physics behind the redox reaction and its cyclic performance. Study of the physics of materials during the storage/release cycle is necessary for the design and improvement of the reactor and can be used as a benchmark for comparison of any implemented changes. A high precision, true differential TGA/DSC instrument is used for simultaneous measurement of weightchange (TGA) and true differential heat flow (DSC) for pure cobalt oxide (Co3O4) powder. Storage cycle (charge/discharge) was conducted for five cycles. Complete re-oxidation was achieved within reasonable times by performing the two reactions at close temperatures and controlling heating/cooling rates. Basic performance parameters were derived as a benchmark for future references. Single-cycle controlling parameters such as heating/cooling rate, dwelling time, and purge gas rate were investigated. System response for few initial cycles was studied. It was shown that pure cobalt oxide could regain weight and complete re-oxidation with reasonable stability. A transition for heat flow was detected after a few initial cycles which reduced discharge heat and decreased overall performance.

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Abe, Toshiaki, Takashi Sugiura, Shuji Okunaga, Katsuhiro Nojima, Yasukata Tsutsui, and Takayuki Matsunuma. "Research and Development of Practical Industrial Cogeneration Technology in Japan." In ASME Turbo Expo 2000: Power for Land, Sea, and Air. American Society of Mechanical Engineers, 2000. http://dx.doi.org/10.1115/2000-gt-0655.

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This paper presents an overview of a development project involving industrial cogeneration technology using 8,000-kW class hybrid gas turbines in which both metal and ceramics are used in parts subject to high temperatures in order to achieve high efficiency and low pollution. The development of hybrid gas turbines focuses mainly on the earlier commercialization of the turbine system. Stationary parts such as combustor liners, transition ducts, and first-stage turbine nozzles (stationary blades) are expected to be fabricated from ceramics. The project aims at developing material for these ceramic parts that will have a superior resistance to heat and oxidation. The project also aims at designing and prototyping a hybrid gas turbine system to analyze the operation in order to improve the performance. Furthermore, the prototyped hybrid gas turbine system will be tested for long-term operation (4,000 hours) to verify that the system can withstand commercialization. Studies will be conducted to ensure that the system’s soundness and reliability are sufficient for industrial cogeneration applications.

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Reports on the topic "Oxidation Transition metal halides"

1

Chen, A. L., and P. Y. Yu. Charge-transfer gap closure in transition-metal halides under pressure. Office of Scientific and Technical Information (OSTI), January 1995. http://dx.doi.org/10.2172/69161.

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Doerrer, Linda H. Development of Earth-Abundant Transition Metal Compounds for Water Oxidation. Office of Scientific and Technical Information (OSTI), January 2019. http://dx.doi.org/10.2172/1489778.

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Carraher, Jack McCaslin. Kinetic and mechanistic studies of reactive intermediates in photochemical and transition metal-assisted oxidation, decarboxylation and alkyl transfer reactions. Office of Scientific and Technical Information (OSTI), January 2014. http://dx.doi.org/10.2172/1226564.

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Klier, Kamil, Jean Paul Lange, and Richard G. Herman. Partial oxidation of light alkanes in transition metal ion containing zeolites: Quarterly technical progress report for the period December 15, 1988--March 14, 1989. Office of Scientific and Technical Information (OSTI), April 1989. http://dx.doi.org/10.2172/6431598.

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