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Artykuły w czasopismach na temat "Modern catalysis"
Zhao, Xiaodan, i Lihao Liao. "Modern Organoselenium Catalysis: Opportunities and Challenges". Synlett 32, nr 13 (11.05.2021): 1262–68. http://dx.doi.org/10.1055/a-1506-5532.
Pełny tekst źródłaHooper, Reviewed by Mark. "Modern Palladium Catalysis". Platinum Metals Review 49, nr 2 (1.04.2005): 77–78. http://dx.doi.org/10.1595/147106705x46487.
Pełny tekst źródłaWilkins, Lewis C., i Rebecca L. Melen. "Enantioselective Main Group Catalysis: Modern Catalysts for Organic Transformations". Coordination Chemistry Reviews 324 (październik 2016): 123–39. http://dx.doi.org/10.1016/j.ccr.2016.07.011.
Pełny tekst źródłaStrekalova, Anna A., Anastasiya A. Shesterkina i Leonid M. Kustov. "Recent progress in hydrogenation of esters on heterogeneous bimetallic catalysts". Catalysis Science & Technology 11, nr 22 (2021): 7229–38. http://dx.doi.org/10.1039/d1cy01603b.
Pełny tekst źródłaSambiagio, Carlo, Stephen P. Marsden, A. John Blacker i Patrick C. McGowan. "Copper catalysed Ullmann type chemistry: from mechanistic aspects to modern development". Chem. Soc. Rev. 43, nr 10 (2014): 3525–50. http://dx.doi.org/10.1039/c3cs60289c.
Pełny tekst źródłaTrunschke, Annette, Giulia Bellini, Maxime Boniface, Spencer J. Carey, Jinhu Dong, Ezgi Erdem, Lucas Foppa i in. "Towards Experimental Handbooks in Catalysis". Topics in Catalysis 63, nr 19-20 (6.10.2020): 1683–99. http://dx.doi.org/10.1007/s11244-020-01380-2.
Pełny tekst źródłaNachtsheim, Boris, i Peter Finkbeiner. "Iodine in Modern Oxidation Catalysis". Synthesis 45, nr 08 (21.03.2013): 979–99. http://dx.doi.org/10.1055/s-0032-1318330.
Pełny tekst źródłaLapina, Olga B. "Modern ssNMR for heterogeneous catalysis". Catalysis Today 285 (maj 2017): 179–93. http://dx.doi.org/10.1016/j.cattod.2016.11.005.
Pełny tekst źródłaKunz, Doris. "Modern Metallocene Chemistry and Catalysis". Nachrichten aus der Chemie 52, nr 10 (październik 2004): 1085. http://dx.doi.org/10.1002/nadc.20040521032.
Pełny tekst źródłaMuldoon, Mark J. "Modern multiphase catalysis: new developments in the separation of homogeneous catalysts". Dalton Trans. 39, nr 2 (2010): 337–48. http://dx.doi.org/10.1039/b916861n.
Pełny tekst źródłaRozprawy doktorskie na temat "Modern catalysis"
Werner, Emilie. "Catalysis at the origin of life and catalysis today, a 3.8-billion-year jump". Electronic Thesis or Diss., Strasbourg, 2024. https://publication-theses.unistra.fr/public/theses_doctorat/2024/Werner_Emilie_2024_ED222.pdf.
Pełny tekst źródłaCatalysis enables selective and enhanced reactivity and is harnessed in both synthetic chemistry and biology. This thesis will discuss this concept at two different time points. Firstly, the chemical processes at the origins of life will be studied through two types of non-enzymatic catalysis: rare metal catalysis and metal/coenzyme cocatalysis. The latter is thought to be a product of evolution to become independent from rare environments and enable prebiotic chemistry to spread to more common media. Secondly, modern metal catalysis will be examined. A new aza-variant of the Piancatelli rearrangement will be described with sulfoximine nucleophiles, giving direct access to unprecedented 4-sulfoximinocyclopentenone scaffolds in good yields. These structures hold promises for applications in drug discovery
Falletta, E. "¿RE-DISCOVERING¿ AN OLD MATERIAL, POLYANILINE, FOR MODERN APPLICATIONS". Doctoral thesis, Università degli Studi di Milano, 2014. http://hdl.handle.net/2434/229552.
Pełny tekst źródłaSharma, Giriraj. "Modeling of selective catalytic reduction (SCR) of nitric oxide with ammonia using four modern catalysts". Texas A&M University, 2004. http://hdl.handle.net/1969.1/2785.
Pełny tekst źródłaFilippov, Igor 1971. "Metal-mediated hydrodenitrogenation catalysis: Designing new models". Diss., The University of Arizona, 1998. http://hdl.handle.net/10150/282749.
Pełny tekst źródłaHuang, Jin-Mo. "Model Development for the Catalytic Calcination of Calcium Carbonate". Thesis, North Texas State University, 1987. https://digital.library.unt.edu/ark:/67531/metadc331193/.
Pełny tekst źródłaPagani, Adriana Siviero. "Estudo cinetico do craqueamento catalitico de moleculas modelo de hidrocarbonetos em catalisadores de FCC". [s.n.], 2009. http://repositorio.unicamp.br/jspui/handle/REPOSIP/267085.
Pełny tekst źródłaTese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Quimica
Made available in DSpace on 2018-08-13T11:29:24Z (GMT). No. of bitstreams: 1 Pagani_AdrianaSiviero_D.pdf: 5130407 bytes, checksum: b53a0b1f8d58411a68c3cb683c12eba0 (MD5) Previous issue date: 2009
Resumo: O 1-octeno, 2,2,4-trimetil-pentano e n-octano foram utilizados como moléculas modelo para o estudo experimental e de modelagem do craqueamento catalítico na superfície de dois catalisadores comerciais (PETROBRAS), compostos por zeólita USY e matriz (SiO2-Al2O3) com impregnação de terras raras (CTR) e sem a impregnação de terras raras (STR), ambos desativados pelo método vapor. Os testes de craqueamento catalítico foram realizados em fase gasosa em reator tubular de leito fixo, construído em quartzo, na faixa de temperatura de 325 a 685 K para o 1-octeno, 725 a 950 K para o 2,2,4-trimetil-pentano e 815 a 975 K para o n-octano à pressão atmosférica. O catalisador STR apresentou valores de taxa de giro (s-1) maiores que os encontrados para o CTR. As energias de ativação aparente apresentaram a seguinte ordem decrescente: n-octano (STR: 180 kJ mol-1 e CTR: 192 kJ mol-1) > 2,2,4-trimetil-pentano (STR: 121 kJ mol-1 / CTR: 127 kJ mol-1) > 1-octeno (STR: 18 kJ mol-1 / CTR: 23 kJ mol-1). Os mecanismos de reações foram determinados para as três moléculas modelo através dos produtos de reação determinados experimentalmente e considerando as famílias de reações de iniciação, isomerização, transferência de hidrogênio, adsorção/dessorção e cisão-ß/oligomerização. A modelagem do craqueamento catalítico foi desenvolvida segundo a teoria da colisão, a teoria do estado de transição e as propriedades termodinâmicas das espécies envolvidas nos mecanismos. As taxas de giro da modelagem cinética apresentaram uma diferença com as taxas de giro experimentais de aproximadamente 20%.
Abstract: The 1-octene, 2,2,4-trimethylpentane and n-octane were used as model molecules in an experimental and modeling study for the catalytic cracking on the surface of commercial catalysts (PETROBRAS) that are composed of USY zeolite and matrix with rare earth impregnation (CTR) and without rare earth impregnation (STR), both deactivated by steam method. The experimental tests were carried out in the gas phase, in a fixed bed tubular reactor made of quartz in the temperature range of 325 to 685 K for the 1-octene, 725 to 950 K for the 2,2,4-trimethylpentane and 815 to 975 K for the n-octane at atmospheric pressure. The catalyst STR showed higher values of turnover rate (s-1) than the catalyst CTR. The apparent activation energies showed the following decreasing order: n-octane (STR: 180 kJ mol-1 and CTR: 192 kJ mol-1) > 2,2,4-trimethylpentane (STR: 121 kJ mol-1 / CTR: 127 kJ mol-1) > 1-octene (STR: 18 kJ mol-1 / CTR: 23 kJ mol-1). The reactions mechanisms were determined for the three model molecules with the reaction products obtained experimentally and considering the families of reactions of initiation, isomerization, hydride transfer, adsorption/desorption and ß-scission/oligomerization. The modeling of the catalytic cracking was developed according to the collision theory, the transition state theory and the thermodynamics properties of the adsorbed species involved in the mechanisms. The model turnover rates showed a difference between the experimental turnover rates near 20 %.
Doutorado
Desenvolvimento de Processos Químicos
Doutor em Engenharia Química
Harle, Gavin John. "Polyoxometalate models for Fischer-Tropsch Catalysts". Thesis, University of Newcastle Upon Tyne, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.519568.
Pełny tekst źródłaHayward, J. J. "Studies in modern organic chemistry : catalytic, technological and structural". Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603905.
Pełny tekst źródłaNdi, Cornelius Ndi. "Synthesis of Chemical Models of Hydrolase Enzymes for Intramolecular Catalysis". Digital Commons @ East Tennessee State University, 2011. https://dc.etsu.edu/etd/1356.
Pełny tekst źródłaIsenogle, Melanie R. "Anna Atkins: Catalyst of Modern Photography Through The First Photobook". Bowling Green State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1522796885194359.
Pełny tekst źródłaKsiążki na temat "Modern catalysis"
R, Moser William, red. Advanced catalysts and nanostructured materials: Modern synthetic methods. San Diego: Academic Press, 1996.
Znajdź pełny tekst źródłavan Santen, Rutger A., red. Modern Heterogeneous Catalysis. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527810253.
Pełny tekst źródłaChorkendorff, I. Concepts of modern catalysis and kinetics. Weinheim: Wiley-VCH, 2004.
Znajdź pełny tekst źródłaChorkendorff, I. Concepts of modern catalysis and kinetics. Weinheim [Germany]: Wiley-VCH, 2003.
Znajdź pełny tekst źródłaChorkendorff, I. Concepts of modern catalysis and kinetics. Wyd. 2. Weinheim: Wiley-VCH, 2007.
Znajdź pełny tekst źródłaMizuno, Noritaka. Modern heterogeneous oxidation catalysis: Design, reactions and characterization. Weinheim: Wiley-VCH, 2009.
Znajdź pełny tekst źródłaFessner, W. D. Modern biocatalysis: Stereoselective and environmentally friendly reactions. Weinheim: Wiley-VCH, 2009.
Znajdź pełny tekst źródłaDoyle, Michael P. Modern catalytic methods for organic synthesis with diazo compounds: From cyclopropanes to ylides. New York: Wiley, 1998.
Znajdź pełny tekst źródłaLeszczyński, Jerzy. Multi-scale Quantum Models for Biocatalysis: Modern Techniques and Applications. Dordrecht: Springer Netherlands, 2009.
Znajdź pełny tekst źródła1942-, Occelli Mario L., American Chemical Society. Division of Petroleum Chemistry. i American Chemical Society Meeting, red. Fluid catalytic cracking: Role in modern refining. Washington, DC: American Chemical Society, 1988.
Znajdź pełny tekst źródłaCzęści książek na temat "Modern catalysis"
Osawa, Tsutomu. "Heterogeneous Catalysis". W Modern Organonickel Chemistry, 273–305. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527604847.ch10.
Pełny tekst źródłaTributsch, H. "Photoelectrolysis and Photoelectrochemical Catalysis". W Modern Aspects of Electrochemistry, 303–55. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2133-0_4.
Pełny tekst źródłaKasey, Christian, i Gavin J. Williams. "Chapter 8. Customizing Transcription-factor Biosensors for Modern Biotechnology". W Catalysis Series, 203–33. Cambridge: Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/9781788010450-00203.
Pełny tekst źródłaSinou, Denis. "Metal Catalysis in Water". W Modern Solvents in Organic Synthesis, 41–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-48664-x_2.
Pełny tekst źródłaPark, Joo-Il, Isao Mochida, Abdulazeem M. J. Marafi i Adel Al-Mutairi. "Modern Approaches to Hydrotreating Catalysis". W Springer Handbook of Petroleum Technology, 675–712. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-49347-3_21.
Pełny tekst źródłaDagorne, Samuel, i Christophe Fliedel. "Organoaluminum Species in Homogeneous Polymerization Catalysis". W Modern Organoaluminum Reagents, 125–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/3418_2012_35.
Pełny tekst źródłaNoyori, R., i M. Kitamura. "Enantioselective Catalysis with Metal Complexes. An Overview". W Modern Synthetic Methods, 115–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83758-6_2.
Pełny tekst źródłaRusling, James F. "Electrochemistry and Electrochemical Catalysis in Microemulsions". W Modern Aspects of Electrochemistry, 49–104. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1733-1_2.
Pełny tekst źródłaThomas, John M., i Thomas Maschmeyer. "The Changing Face of Modern Catalysis". W New Trends in Materials Chemistry, 363–76. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5570-0_13.
Pełny tekst źródłaPfaltz, Andreas. "Enantioselective Catalysis with Chiral Cobalt and Copper Complexes". W Modern Synthetic Methods, 199–248. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83758-6_3.
Pełny tekst źródłaStreszczenia konferencji na temat "Modern catalysis"
Li, Mingtian, Hong Wang, Lanying Yu i RuiSong Yang. "Solid-state synthesis and catalysis property of copper phthalocyanine". W International Conference on Modern Engineering Soultions for the Industry. Southampton, UK: WIT Press, 2014. http://dx.doi.org/10.2495/mesi141252.
Pełny tekst źródłaChu, Ranran, Hui Wang, Xinxin Wang, Li Han i Weijuan Gong. "Research on Teaching Reform of Industrial Catalysis Course Based on Ability Training". W 2020 5th International Conference on Modern Management and Education Technology (MMET 2020). Paris, France: Atlantis Press, 2020. http://dx.doi.org/10.2991/assehr.k.201023.079.
Pełny tekst źródłaНурмахаматов, Герман Владимирович, i Владислав Сергеевич Хрипко. "IMPROVING THE ENERGY EFFICIENCY OF THE REFINING PROCESS BY THE EXAMPLE OF THE ISOMERIZATION PROCESS". W Наука, общество, производство и промышленность: актуальные проблемы и перспективы: сборник статей международной научной конференции (Омск, Апрель 2023). Crossref, 2023. http://dx.doi.org/10.37539/230407.2023.66.59.002.
Pełny tekst źródłaJayasuriya, Jeevan, Arturo Manrique, Reza Fakhrai, Jan Fredriksson i Torsten Fransson. "Experimental Investigations of Catalytic Combustion for High-Pressure Gas Turbine Applications". W ASME Turbo Expo 2006: Power for Land, Sea, and Air. ASMEDC, 2006. http://dx.doi.org/10.1115/gt2006-90986.
Pełny tekst źródłaBerahim, Nor Hafizah, i Akbar Abu Seman. "CO2 Utilization: Converting Waste into Valuable Products". W SPE Asia Pacific Oil & Gas Conference and Exhibition. SPE, 2022. http://dx.doi.org/10.2118/210729-ms.
Pełny tekst źródłaZhang, Bo, Pengfei He i Chao Zhu. "Modeling on Hydrodynamic Coupled FCC Reaction in Gas-Solid Riser Reactor". W ASME 2014 4th Joint US-European Fluids Engineering Division Summer Meeting collocated with the ASME 2014 12th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/fedsm2014-21368.
Pełny tekst źródłaZhu, Huayang, i Greg S. Jackson. "Transient Modeling for Assessing Catalytic Combustor Performance in Small Gas Turbine Applications". W ASME Turbo Expo 2001: Power for Land, Sea, and Air. American Society of Mechanical Engineers, 2001. http://dx.doi.org/10.1115/2001-gt-0520.
Pełny tekst źródłaWilson, John Parley, i Dan DelVescovo. "Algorithm to Calibrate Catalytic Converter Simulation Light-Off Curve". W WCX SAE World Congress Experience. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2024. http://dx.doi.org/10.4271/2024-01-2630.
Pełny tekst źródłaDepcik, Christopher, Sudarshan Loya i Anand Srinivasan. "Adaptive Carbon Monoxide Kinetics for Exhaust Aftertreatment Modeling". W ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-11173.
Pełny tekst źródłaBottomley, D. J., G. Lüpke i H. M. van Driel. "Second-harmonic probing of the Si(100) - SiO2 interface on flat and vicinal Si(100): interfacial structure and step binding sites". W Nonlinear Optics. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/nlo.1992.tha8.
Pełny tekst źródłaRaporty organizacyjne na temat "Modern catalysis"
Boszormenyi, Istvan. Model heterogeneous acid catalysts and metal-support interactions: A combined surface science and catalysis study. Office of Scientific and Technical Information (OSTI), maj 1991. http://dx.doi.org/10.2172/10115869.
Pełny tekst źródłaBoszormenyi, I. Model heterogeneous acid catalysts and metal-support interactions: A combined surface science and catalysis study. Office of Scientific and Technical Information (OSTI), maj 1991. http://dx.doi.org/10.2172/6827194.
Pełny tekst źródłaChapman i Toema. PR-266-09211-R01 Physics-Based Characterization of Lambda Sensor from Natural Gas Fueled Engines. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), listopad 2012. http://dx.doi.org/10.55274/r0010022.
Pełny tekst źródłaHenrich, V. Model catalyst studies of active sites and metal support interactions on vanadia and vanadia-supported catalysts. Office of Scientific and Technical Information (OSTI), wrzesień 1989. http://dx.doi.org/10.2172/5484103.
Pełny tekst źródłaSchneider, William. Towards Realistic Models of Heterogeneous Catalysis: Simulations of Oxidation Catalysis from First Principles. Office of Scientific and Technical Information (OSTI), grudzień 2021. http://dx.doi.org/10.2172/1835236.
Pełny tekst źródłaAnderson, Scott. Model catalysis by size-selected cluster deposition. Office of Scientific and Technical Information (OSTI), listopad 2015. http://dx.doi.org/10.2172/1226465.
Pełny tekst źródłaGorte, R. G. Support effects studied on model supported catalysts. Office of Scientific and Technical Information (OSTI), listopad 1991. http://dx.doi.org/10.2172/5576394.
Pełny tekst źródłaGorte, R. J. Support effects studied on model supported catalysts. Office of Scientific and Technical Information (OSTI), luty 1993. http://dx.doi.org/10.2172/6854889.
Pełny tekst źródłaMarks, Tobin J., Madelyn M. Stalzer i Massimiliano Delferro. Supported Organometallic Complexes: Surface Chemistry, Spectroscopy, Catalysis, and Homogeneous Models. Office of Scientific and Technical Information (OSTI), wrzesień 2016. http://dx.doi.org/10.2172/1325016.
Pełny tekst źródłaMadey, T. E. Structure and reactivity of model thin film catalysts. Office of Scientific and Technical Information (OSTI), sierpień 1989. http://dx.doi.org/10.2172/7168433.
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