Gold and Silver Catalysts for Liquid Phase n-Octanol Oxidation: Effect of Promoters; Current Organic Synthesis; Vol. 14, iss. 3

Podrobná bibliografie
Parent link:Current Organic Synthesis.— , 2004-
Vol. 14, iss. 3.— 2017.— [P. 323 - 331]
Korporativní autor: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра физической и аналитической химии (ФАХ)
Další autoři: Kotolevich Yu. I. Yuliya, Kolobova E. N. Ekaterina Nikolaevna, Pestryakov A. N. Aleksey Nikolaevich, Cabrera O. J. E. Ortega Jesus Efren, Bogdanchikova N. E. Nina Evgenjevna, Cortes C. V. Corberan, Khramov Evgeny E. A., Zubavichus Ya. V. Yan Vitautasovich, Zanella Rodolfo R. A., Pakrieva E. G. Ekaterina Germanovna
Shrnutí:Title screen
Background: In comparison with these platinum group metal catalysts, supported nano gold catalysts have emerged as a new type of catalysts highly active at low temperature and selective for the aerobic oxidation of alcohols. But catalytic data and detailed characterizations of the Au-Ag bimetal catalytic system are not available up to date.Objective: This work is aimed to develop bimetallic AuAg-based heterogeneous catalysts for liquid phase selective oxidation of n-octanol. Modification of the titania support with transition metal additives were used as tools for transforming active species.Method: Catalytic tests in n-octanol liquid-phase oxidation at 80 °C. Catalyst characterization by Transmission electron microscopy, X-ray diffraction, plasma atomic emission spectroscopy, X-ray photoelectron spectroscopy, EXAFS and UV-visible spectroscopy.Results and Conclusion: Bimetallic AuAg catalysts supported on titania are moderately active for liquid phase selective oxidation of n-octanol. Formation of Au-Ag alloy was observed. Their activity may be increased by modification of the support with donor additives (La, Mg), while acceptor additives (Ce, Fe) decreased it. The addition of La, that inhibits the formation of Au-Ag alloy, provides the highest activity and the highest stability of reaction rate with run time in either as prepared and red-ox treated forms, which implies that it stabilizes the active centers in its optimal electronic state.
Режим доступа: по договору с организацией-держателем ресурса
Jazyk:angličtina
Vydáno: 2017
Témata:
On-line přístup:https://doi.org/10.2174/1570179413666161031113854
Médium: Elektronický zdroj Kapitola
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=654871

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200 1 |a Gold and Silver Catalysts for Liquid Phase n-Octanol Oxidation: Effect of Promoters  |f Yu. I. Kotolevich [et al.] 
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330 |a Background: In comparison with these platinum group metal catalysts, supported nano gold catalysts have emerged as a new type of catalysts highly active at low temperature and selective for the aerobic oxidation of alcohols. But catalytic data and detailed characterizations of the Au-Ag bimetal catalytic system are not available up to date.Objective: This work is aimed to develop bimetallic AuAg-based heterogeneous catalysts for liquid phase selective oxidation of n-octanol. Modification of the titania support with transition metal additives were used as tools for transforming active species.Method: Catalytic tests in n-octanol liquid-phase oxidation at 80 °C. Catalyst characterization by Transmission electron microscopy, X-ray diffraction, plasma atomic emission spectroscopy, X-ray photoelectron spectroscopy, EXAFS and UV-visible spectroscopy.Results and Conclusion: Bimetallic AuAg catalysts supported on titania are moderately active for liquid phase selective oxidation of n-octanol. Formation of Au-Ag alloy was observed. Their activity may be increased by modification of the support with donor additives (La, Mg), while acceptor additives (Ce, Fe) decreased it. The addition of La, that inhibits the formation of Au-Ag alloy, provides the highest activity and the highest stability of reaction rate with run time in either as prepared and red-ox treated forms, which implies that it stabilizes the active centers in its optimal electronic state. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
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463 |t Vol. 14, iss. 3  |v [P. 323 - 331]  |d 2017 
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