Relevant bibliographies by topics / Catalysis by sulfides

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Catalysis by sulfides'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "Catalysis by sulfides"

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Kadikova, Rita, Ilfir Ramazanov, Alexey Vyatkin, and Usein Dzhemilev. "Zirconium-Catalyzed Reaction of 1-Alkynyl Sulfides with Et3Al: A Novel Route to Trisubstituted 1-Alkenyl Sulfides." Synlett 29, no. 13 (2018): 1773–75. http://dx.doi.org/10.1055/s-0037-1610431.

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The reaction of 1-alkynyl sulfides and alkynyl sulfoxides with Et3Al under zirconocene catalysis conditions has been studied. The interaction between 1-alkynyl sulfides and Et3Al in the presence of catalytic amounts of Cp2ZrCl2 leads to trisubstituted 1-alkenyl sulfides in moderate to good yields (56–73%) with high regioselectivity and stereo­selectivity. 1-Alkynyl sulfoxides, upon treatment with Et3Al under the same reaction conditions, undergoes reduction to give sulfides. The excess of Et3Al (7 equiv) in this reaction causes cyclic carboalumination of in situ generated 1-alkynyl sulfide to
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Marques, Antonio, Massimo di Matteo, and Marie-Françoise Ruasse. "Remarkable efficiency of iron(III) versus manganese(III) tetraphenylporphyrins as catalysts for fast and quantitative oxidation of sulfides into sulfones by hydrogen peroxide." Canadian Journal of Chemistry 76, no. 6 (1998): 770–75. http://dx.doi.org/10.1139/v98-050.

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The efficiency of various metallo-phtalocyanines (Pht) and -tetraphenylporphyrins (TPP) as catalysts for the H2O2 oxidations of dibenzylsulfide, phenylchloroethylsulfide, and thioanisole is investigated in ethanol and acetonitrile, using imidazole as a cocatalyst. Neither PhtNiII nor TPPCoII exhibits any catalytic activity. PhtMnII and TPPMnIIICl accelerate markedly these reactions but do not promote quantitative oxidations, at most 70% of the sulfides being transformed into sulfoxides. In contrast, with PhtFeII sulfoxides are obtained with a 100% yield from sulfides. Finally, the only catalys
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Bunton, Clifford A., Houshang J. Foroudian, Nicholas D. Gillitt, and Anurag Kumar. "Article." Canadian Journal of Chemistry 77, no. 5-6 (1999): 895–902. http://dx.doi.org/10.1139/v99-057.

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Oxidations of sulfides and phosphorus(V) esters of thiols by H2O2 are catalyzed by H2SO4 and HClO4. Sulfides are 4-ZC6H4SMe, 1a-1e, respectively, Z = MeO, Me, H, Cl, NO2; PhSCH2CH2Cl, 2, Ph2S, 3, and the esters are Ph(R)PO·SEt, 4a, 4b, R = Ph, EtO. Electron donation by Z moderately accelerates reaction, but the sulfides are much more reactive than the esters. Reactions are first order in H2O2 and substrate, and second-order rate constants, k2, in H2SO4 are related to excess acidity, X. Plots of log k2 against X have slopes in the range 0.61-0.85. Rate constants are similar for given concentrat
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Pimerzin, Aleksey, Aleksander Savinov, Anna Vutolkina, et al. "Transition Metal Sulfides- and Noble Metal-Based Catalysts for N-Hexadecane Hydroisomerization: A Study of Poisons Tolerance." Catalysts 10, no. 6 (2020): 594. http://dx.doi.org/10.3390/catal10060594.

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Bifunctional catalysts on the base of transition metal sulfides (CoMoS and NiWS) and platinum as noble metal were synthesized via wetness impregnation of freshly synthesized Al2O3-SAPO-11 composites, supported with favorable acidic properties. The physical-chemical properties of the prepared materials were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), low-temperature N2 adsorption and high resolution transmission electron microscopy (HR TEM) methods. Catalytic properties were studied in n-hexadecane isomerization using a fixed-bed flow reactor. The catalytic poisons t
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Ranu, Brindaban C., Tanmay Mandal, Subhash Banerjee та Suvendu S. Dey. "Ionic Liquid Promoted Regio- and Stereo-Selective Thiolysis of Epoxides—A Simple and Green Approach to β-Hydroxy- and β-Keto Sulfides". Australian Journal of Chemistry 60, № 4 (2007): 278. http://dx.doi.org/10.1071/ch06434.

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A variety of epoxides underwent facile cleavage by thiols under the catalysis of 1-methyl-3-butylimidazolium bromide, [bmIm]Br, to produce the corresponding β-hydroxy sulfides with high regio- and stereo-selectivity. On the other hand, a specially designed basic ionic liquid, [bmIm]OH, efficiently catalyzes the thiolysis of α,β-epoxy ketones providing β-keto sulfides through simultaneous retro-aldol cleavages. The reactions are clean, high yielding, and do not require any organic solvent. The catalyst is also recycled.
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Han, Qilin, Yadong Yang, Ruofan Wang, Kai Zhang, Na Liu, and Mei Hong. "Biochar Derived from Agricultural Wastes as a Means of Facilitating the Degradation of Azo Dyes by Sulfides." Catalysts 11, no. 4 (2021): 434. http://dx.doi.org/10.3390/catal11040434.

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Dyes are common contaminants, some of which are teratogenic, carcinogenic, and causative of ecological damage, and dye wastewater often contains toxic sulfides. Biochar has been widely used for the adsorption and catalysis degradation of pollutants, including dyes and sulfides, due to its abundant surface functional groups and large specific surface area. Therefore, the simultaneous treatment of dyes and sulfides with biochar may be a feasible, effective, and novel solution. This study sought to utilize low-cost, environmentally friendly, and widely sourced biochar materials from agricultural
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Zhang, Yimin, Iiu, and Junmin Chen. "Efficient Synthesis of Diaryl Sulfides by Copper-catalysed Coupling of Aryl Halides and Thioacetate in Water." Journal of Chemical Research 37, no. 1 (2013): 19–21. http://dx.doi.org/10.3184/174751912x13545509224571.

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A simple economical, and highly efficient catalytic system for the synthesis of diaryl sulfides by a copper-catalysed coupling of aryl halides and thioacetate in water has been developed. A variety of aryl halides reacted with thioacetate to give the desired products in high yields up to 95%. The present catalysis protocol tolerated a wide range of functional groups, including amino, fluoro, and carboxyl moieties.
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Alvarez-Galvan, M., Jose Campos-Martin, and Jose Fierro. "Transition Metal Phosphides for the Catalytic Hydrodeoxygenation of Waste Oils into Green Diesel." Catalysts 9, no. 3 (2019): 293. http://dx.doi.org/10.3390/catal9030293.

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Recently, catalysts based on transition metal phosphides (TMPs) have attracted increasing interest for their use in hydrodeoxygenation (HDO) processes destined to synthesize biofuels (green or renewable diesel) from waste vegetable oils and fats (known as hydrotreated vegetable oils (HVO)), or from bio-oils. This fossil-free diesel product is produced completely from renewable raw materials with exceptional quality. These efficient HDO catalysts present electronic properties similar to noble metals, are cost-efficient, and are more stable and resistant to the presence of water than other class
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Cibulka, Radek, Lenka Baxová, Hana Dvořáková, et al. "Catalytic effect of alloxazinium and isoalloxazinium salts on oxidation of sulfides with hydrogen peroxide in micellar media." Collection of Czechoslovak Chemical Communications 74, no. 6 (2009): 973–93. http://dx.doi.org/10.1135/cccc2009030.

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Three novel amphiphilic alloxazinium salts were prepared: 3-dodecyl-5-ethyl-7,8,10-trimethylisoalloxazinium perchlorate (1c), 1-dodecyl-5-ethyl-3-methylalloxazinium perchlorate (2b), and 3-dodecyl-5-ethyl-1-methylalloxazinium perchlorate (2c). Their catalytic activity in thioanisole (3) oxidation with hydrogen peroxide was investigated in micelles of sodium dodecylsulfate (SDS), hexadecyltrimethylammonium nitrate (CTANO3) and Brij 35. Reaction rates were strongly dependent on the catalyst structure, on the type of micelles, and on pH value. Alloxazinium salts 2 were more effective catalysts th
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Grutza, Marie-Luise, Ashwene Rajagopal, Carsten Streb, and Philipp Kurz. "Hydrogen evolution catalysis by molybdenum sulfides (MoSx): are thiomolybdate clusters like [Mo3S13]2− suitable active site models?" Sustainable Energy & Fuels 2, no. 9 (2018): 1893–904. http://dx.doi.org/10.1039/c8se00155c.

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Recent results concerning molecular molybdenum sulfido clusters as model systems for heterogeneous hydrogen evolution catalysis by molybdenum sulfides are summarized and also compared to the related chemistry of the active site of the enzyme Mo-nitrogenase.
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Dissertations / Theses on the topic "Catalysis by sulfides"

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Myllymäki, V. (Vesa). "Design, synthesis and testing of new chiral sulfide catalysts for Corey-Chaykovsky reaction." Doctoral thesis, University of Oulu, 2001. http://urn.fi/urn:isbn:9514265718.

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Abstract The first part of this monograph discusses the asymmetric, ylide based, reagent controlled epoxidations. Both different chiral ylides and epoxidation processes, stoichiometric and catalytic, are reviewed. In the following part, new chiral sulfide catalysts were discovered as enantioselective catalysts for the Corey-Chaykovsky reaction (epoxidation of aldehydes via sulfonium ylides). Using a crystal structure of an oxazolidine derivative as a starting point, a thiazolidine ligand family was designed, synthesized and finally employed as catalysts in the asymmetric epoxidation
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Chamberlin, Rachel Alexandra. "Some substitution reactions of aryl sulfides and aryl ethers with aliphatic amines in DMSO : the mechanism of base catalysis." Thesis, Durham University, 1995. http://etheses.dur.ac.uk/5213/.

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The reactions of several nitro-aromatic substrates with the aliphatic amines, n- butylamine, pyrrolidine and piperidine in DMSO have been studied. Reaction of the amines with trinitroaromatic compounds, such as ethyl thiopicrate, phenyl thiopicrate and phenyl 2,4,6-trinitrophenyl ether, was shown to occur in two well separated processes. A rapid reaction, occuring at an unsubstituted ring position, resulted in the formation of a a-adduct; this was followed by a slower substitution reaction, resulting in the displacement of the 1-substituent to give the amino-substituted compound. Kinetic resul
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Lakhdar, Mahjoub. "Application de la reaction d'hydrodesazotation de la pyridine a la caracterisation de l'activite et de la selectivite de catalyseurs sulfures." Caen, 1987. http://www.theses.fr/1987CAEN2021.

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KAMYAB, ALI. "Preparation and evaluation of sulfided NiMo/γ-Al2O3 hydrotreating catalysts". Thesis, KTH, Skolan för kemivetenskap (CHE), 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-190904.

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Four nickel-molybdenum catalysts were synthesized on gamma alumina with higher surface area and on NiMo catalyst was prepared using gamma alumina with lower surface area. Catalysts with higher-surface-area support were prepared by co-impregnation, sequential impregnation and adding phosphorous. Theses catalysts were calcined at 500  ͦC. Effect of higher calcination temperature was investigated by preparation of one catalyst calcined at 700 ͦC. Catalysts were thoroughly characterized via four characterization techniques. The hydrotreating activity of three catalysts was carried out in a micro r
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Catherin, Nelly. "Selective ring opening of naphthenes over bifunctional catalysts in the presence of H2S." Thesis, Lyon, 2016. http://www.theses.fr/2016LYSE1246.

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L'ouverture sélective de cycle (OSC) d'hydrocarbures polycycliques vise à augmenter le nombre de cétane des carburants diesel. OSC efficace peut être atteint par l'hydroconversion sur des catalyseurs bifonctionnels métal noble/fonction acide. La décaline et, à plus faible mesure, le perhydroindane, le butylcyclohexane et la tétraline, ont été utilisés comme molécules modèles pour l'étude des l'OSC de sulfures de métaux de transition (TMSs) supportés sur zéolithes ou silice-alumine amorphe dans un réacteur à lit fixe sous haute pression (5 MPa) avec une concentration élevée d'H2S dans la charge
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Mennour, Ammar. "Caracterisation par spectroscopie infrarouge d'alumines modifiees et de catalyseurs w(mo) - ni(co) sulfures supportes sur alumine." Caen, 1987. http://www.theses.fr/1987CAEN2019.

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Lopes, Silva Susana. "Développement de nouveaux catalyseurs d'hydrotraitement basés sur l'encapsulation d'hétéropolyoxometallates dans des silices mésostructurées : application à la production de carburants propres." Thesis, Lyon, École normale supérieure, 2013. http://www.theses.fr/2013ENSL0799/document.

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Le développement de technologies plus propres et économes en énergie amène aujourd’hui l’industrie du raffinage à modifier ses stratégies de préparation de catalyseurs et à se tourner vers l'utilisation plus massive de catalyseurs hétérogènes plus actifs, sélectifs, stables et régénérables.Récemment une méthode originale a été développée par Dufaud et al. (J. Mater. Chem., 2009, 19, 1142-1150) pour encapsuler des polyoxométallates (POMs) dans les murs des silices mésoporeuses. Le projet de thèse a visé l’élaboration de nouveaux catalyseurs basés sur cette nouvelle méthodologie qui devrait cond
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Hantzer, Sylvain. "Nouveaux materiaux pour la reaction d'hydrodesulfuration (hds)." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13120.

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Nouveau modele de phase active obtenu par interpretation des resultats de rmn du **(59)co et de microscopie electronique haute resolution pour des catalyseurs d'hydrotraitement a base de sulfure de molybdene et de cobalt. Application a d'autres systemes : nire, core, rhre et rhmo. Etude de l'empoisonnement par la porphyrine de catalyseur nimo/al::(2)o::(3)
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Sharma, Gaytri. "Synthesis and characterization of nanostructured Tungsta/Vanadia/Titania catalysts for the oxidation of dimethyl sulfide." Miami University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=miami1228163508.

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Drago, Carmelo. "Combinatorial approaches to catalysis for asymmetric sulfide oxidation." Thesis, University of Sheffield, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.422111.

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Books on the topic "Catalysis by sulfides"

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Russia) International Symposium "Molecular Aspects of Catalysis by Sulfides" (1998 Saint Petersburg. International Symposium "Molecular Aspects of Catalysis by Sulfides", St. Petersburg, Russia: Abstracts. Edited by Parmon, V. N. (Valentin Nikolaevich), Startsev Anatolii N, and Institut kataliza im. G.K. Boreskova. Boreskov Institute of Catalysis, 1998.

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Shiley, R. H. Design principles for a coal desulfurization process with iron sulfides as in situ catalysts. Illinois State Geological Survey, 1986.

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Catalytic Synthesis of Sulfides, Sulfoxides and Sulfones. Harwood Academic Pub, 1991.

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R, Vissers J. P., and Commission of the European Communities. Directorate-General for Science, Research and Development., eds. New sulfide catalysts for the hydroliquefaction of coal. Commission of the European Communities, 1986.

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Fruchtl, Reinhard Alfred *. Catalytic hydrodeoxygenation of phenol, anisole, and guaiacol (wood oil model compounds) using sulfided and unsulfided molybdenum/cobalt/alumina catalysts. 1988.

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Mashinka, A. V. Catalytic Synthesis of Sulfides, Sulfoxides and Sulfones (Sulfur Report, Vol 10, Part 4, 1991). Harwood Academic Pub, 1991.

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Institute of Materials, Minerals, and Mining., ed. A working party report on guidelines on materials requirements for carbon and low alloy steels for H₂S-containing environments in oil and gas production. 3rd ed. Published for the European Federation of Corrosion by Maney Publishing on behalf of the Institute of Materials, Minerals & Mining, 2009.

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Book chapters on the topic "Catalysis by sulfides"

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Griffith, William P. "Oxidations of Amines, Amides, Ethers, Sulfides, Phosphines, Arsines, Stibines and Miscellaneous Substrates." In Catalysis by Metal Complexes. Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-1-4020-9378-4_5.

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CHIANELLI, R. R. "The Role of Solid State Chemistry in Catalysis by Transition Metal Sulfides." In Solid State Chemistry in Catalysis. American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0279.ch013.

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PASQUARIELLO, D. M., R. KERSHAW, J. D. PASSARETTI, K. DWIGHT, and A. WOLD. "Preparation and Properties of Cobalt Sulfide, Nickel Sulfide, and Iron Sulfide." In Solid State Chemistry in Catalysis. American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0279.ch015.

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Montano, P. A., Y. C. Lee, A. Yeye-Odu, and C. H. Chien. "Iron Sulfide Catalysis in Coal Liquefaction." In ACS Symposium Series. American Chemical Society, 1986. http://dx.doi.org/10.1021/bk-1986-0301.ch029.

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Gates, B. C. "Metal Oxide and Metal Sulfide Catalysts." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145319.ch15.

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Kagan, Henri B. "Asymmetric Oxidations and Related Reactions: Asymmetric Oxidation of Sulfides." In Catalytic Asymmetric Synthesis. John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471721506.ch10.

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Harris, Suzanne, and R. R. Chianelli. "Theoretical Studies of Transition Metal Sulfide Hydrodesulfurization Catalysts." In Theoretical Aspects of Heterogeneous Catalysis. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9882-3_6.

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Kakuta, N., J. M. White, A. Campion, et al. "Surface Spectroscopy of Platinum-Cadmium Sulfide-Perfluorosulfonate Polymer Systems." In Catalyst Characterization Science. American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0288.ch046.

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Bouwens, S. M. A. M., D. C. Koningsberger, V. H. J. de Beer, and R. Prins. "Structure of Cobalt Sulfide Phase in Carbon-Supported Co and Co—Mo Sulfide Catalysts." In ACS Symposium Series. American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0411.ch029.

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Towl, A. D. C. "The Influence of Catalysts on the Formation of Hydrogen Sulfide." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145159.ch67.

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Conference papers on the topic "Catalysis by sulfides"

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Du, H., S. H. Ng, K. T. Neo, et al. "Inorganic-Polymer Nanocomposites for Optical Applications." In ASME 2006 Multifunctional Nanocomposites International Conference. ASMEDC, 2006. http://dx.doi.org/10.1115/mn2006-17088.

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The combination of organic and inorganic materials forms unique composites with properties that neither of the two components provides. Such functional materials are considered innovative advanced materials that enable applications in many fields, including optics, electronics, separation membranes, protective coatings, catalysis, sensors, biotechnology, and others. The challenge of incorporating inorganic particles into an organic matrix still remains today, especially for nanoparticles, due to the difficulties in their dispersion, de-agglomeration and surface modification. NanoGram has pione
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Liu, Xiaolu, Yang Liu, Kai Ren, et al. "Clean Energy Generation by a Nanostructured Biophotofuel Cell." In ASME 2013 11th International Conference on Fuel Cell Science, Engineering and Technology collocated with the ASME 2013 Heat Transfer Summer Conference and the ASME 2013 7th International Conference on Energy Sustainability. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/fuelcell2013-18261.

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In this paper, clean energy generation from hazardous materials by a nanostructured biophotofuel cell was studied. Specifically, electrodeposition of polyaniline on TiO2 nanotube as photoelectrochemical anode for a sodium sulfide fuel cell was performed. The photoelectrochemical response of the TiO2 nanotube capped by polyaniline nanoparticles was studied in UV and visible light illumination using sodium sulfide as the electrolyte. The polyaniline was added onto the top end of the nanotube via electrochemical deposition from 0.1 M aniline (C6H7N) in 1 M HCl solution. Polyaniline nanoparticle/T
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Commenges, J., A. M. El-Melih, and A. K. Gupta. "Simulation and Validation of Hydrogen Production From Hydrogen Sulfide Pyrolysis." In ASME 2016 Power Conference collocated with the ASME 2016 10th International Conference on Energy Sustainability and the ASME 2016 14th International Conference on Fuel Cell Science, Engineering and Technology. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/power2016-59036.

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Pyrolysis of hydrogen sulfide has been studied for the treatment of hydrogen sulfide with simultaneous production of hydrogen and sulfur. This novel treatment method has been studied experimentally to provide fundamental information on the overall kinetic parameters. Numerical simulation of thermal pyrolysis of hydrogen sulfide is studied and the results obtained from the modified detailed chemical reaction mechanism are validated with the experimental data. The simulation results agreed favorably well with the experimental data for all examined temperatures up to 1473K. The thermal pyrolysis
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Rleck, Jeffery s., Wilson suarez, and Joseph E. Kubsh. "Development of Non-Nickel Additives for Reducing Hydrogen Sulfide Emissions from Three-way Catalysts." In 1989 SAE International Fall Fuels and Lubricants Meeting and Exhibition. SAE International, 1989. http://dx.doi.org/10.4271/892095.

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Lox, E. S., B. H. Engler, and E. Koberstein. "Development of Scavenger-Free Three-Way Automotive Emission Control Catalysts with Reduced Hydrogen Sulfide Formation." In SAE International Congress and Exposition. SAE International, 1989. http://dx.doi.org/10.4271/890795.

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Yu, Qun, Jingcheng Zhang, Jun Nan, et al. "Synthesis and hydrodesulfurization performance of NiMo sulfide catalysts supported on an Al-Si mixed oxide." In Proceedings of the International Conference on Civil, Architecture and Environmental Engineering (ICCAE2016). CRC Press/Balkema, 2017. http://dx.doi.org/10.1201/9781315116259-64.

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Aswath, P. B., S. Munot, K. Patel, and R. L. Elsenbaumer. "Development and Evaluation of a High Performance Universal Grease." In World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-64079.

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Lithium based grease constitutes a large fraction of the grease consumed in the aviation and automobile industry. The durability and performance of the grease depends upon the additives added. The additive package used here includes PTFE (Poly Tetra-flouroethylene) for low coefficient of friction, ZDDP (Zinc Dialkyl Dithiophosphate) for anti wear properties, and Molybdenum sulfide for high load applications. We have developed a catalyst that helps PTFE to adhere to the metal surface at a low temperature. Block-on-cylinder tests and 4-ball weld tests were carried out to evaluate the effect of t
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NUGRAHANINGTYAS, KHOIRINA DWI, WEGA TRI SUNARYANTI, TRIYONO, NURYONO, DIAN MARUTO WIDJONARKO, and ARI YUSNANI. "THE APPLICATION OF VARIED IMPREGNATION METHODS ON THE CHARACTERS OF NON-SULFIDED NIMO/USY CATALYST." In Proceedings of the International Conference on CBEE 2009. WORLD SCIENTIFIC, 2009. http://dx.doi.org/10.1142/9789814295048_0034.

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Purnomo, F. O., H. Surahman, T. A. Ivandini, S. Naniwa, H. Yoshida, and J. Gunlazuardi. "Bismuth vanadate (BiVO4) as counter electrode in the newly developed catalysis zone of modified cadmium sulfide (CdS) sensitized solar cell for hydrogen production." In PROCEEDINGS OF THE 3RD INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2017 (ISCPMS2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5064101.

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Cayan, Fatma N., Suryanarayana R. Pakalapati, and Ismail Celik. "A Degradation Model for Degradation of Solid Oxide Fuel Cell Anodes due to Impurities in Coal Syngas." In ASME 2011 9th International Conference on Fuel Cell Science, Engineering and Technology collocated with ASME 2011 5th International Conference on Energy Sustainability. ASMEDC, 2011. http://dx.doi.org/10.1115/fuelcell2011-54613.

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A new phenomenological one-dimensional model is formulated to simulate the typical degradation patterns observed in Solid Oxide Fuel Cell (SOFC) anodes due to coal syngas contaminants such as arsenic (As) and phosphorous (P). The model includes gas phase diffusion and surface diffusion within the anode and the adsorption reactions on the surface of the Ni-YSZ-based anode. Model parameters such as reaction rate constants for the adsorption reactions are obtained through indirect calibration to match the degradation rates reported in the literature for arsine (AsH3), phosphine (PH3) and hydrogen
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Reports on the topic "Catalysis by sulfides"

1

Paskach, Thomas Jay. Organusulfur Catalysis With Reduced Molybdenum Sulfides Containing the Mo6S8 Cluster. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/804543.

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2

Becker, Udo, and Rodney Ewing. Actinide Incorporation and Radiation Effects in U(VI) Solids Actinide sorption and reduction on sulfides, oxides, and clay minerals Photoexcitation of Mn-oxide Minerals and Actinide Metal-organic Frameworks for Catalysis of Actinyl Complexes and Nanoclusters. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1615667.

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3

Massoth, F. Comprehensive characterization studies of sulfided molybdenum catalysts. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/5487828.

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4

Klier, K., R. G. Herman, and M. Deemer. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/6737408.

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5

Klier, K., R. G. Herman, M. Richards-Babb, and M. Kieke. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5744996.

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6

Klier, K., and R. G. Herman. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5348544.

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7

Klier, K., R. G. Herman, and M. Richards-Babb. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7233244.

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8

Klier, K., R. G. Herman, and M. Deemer. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/6649378.

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9

K. C. Kwon. Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/901077.

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10

K. C. Kwon. Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/925688.

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