Effect of the Metal Deposition Order on Structural, Electronic and Catalytic Properties of TiO2-Supported Bimetallic Au-Ag Catalysts in 1-Octanol Selective Oxidation; Catalysts; Vol. 11, iss. 7

التفاصيل البيبلوغرافية
Parent link:Catalysts
Vol. 11, iss. 7.— 2021.— [799, 18 p.]
مؤلف مشترك: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
مؤلفون آخرون: Kotolevich Yu. Yulia, Pakrieva E. G. Ekaterina Germanovna, Kolobova E. N. Ekaterina Nikolaevna, Farias M. H. Mario, Bogdanchikova N. Nina, Corberan V. C. Cortes, Pichugina D. A. Daria, Nikitina N. A. Nadezhda, Carabineiro S. A. C. Sonia Alexandra Correia, Pestryakov A. N. Aleksey Nikolaevich
الملخص:Title screen
Au and Ag were deposited on TiO2 modified with Ce, La, Fe or Mg in order to obtain bimetallic catalysts to be used for liquid-phase oxidation of 1-octanol. The effects of the deposition order of gold and silver, and the nature of the support modifying additives and redox pretreatments on the catalytic properties of the bimetallic Au-Ag catalysts were studied. Catalysts were characterized by low-temperature nitrogen adsorption–desorption, energy dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy and ultraviolet-visible diffuse reflectance spectroscopy. It was found that pretreatments with hydrogen and oxygen at 300 °C significantly decreased the activity of AuAg catalysts (silver was deposited first) and had little effect on the catalytic properties of AgAu samples (gold was deposited first). The density functional theory method demonstrated that the adsorption energy of 1-octanol increased for all positively charged AuxAgyq (x + y = 10, with a charge of q = 0 or +1) clusters compared with the neutral counterparts. Lanthanum oxide was a very effective promoter for both monometallic and bimetallic gold and silver catalysts in the studied process.
اللغة:الإنجليزية
منشور في: 2021
الموضوعات:
الوصول للمادة أونلاين:https://doi.org/10.3390/catal11070799
التنسيق: الكتروني فصل الكتاب
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=665407

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200 1 |a Effect of the Metal Deposition Order on Structural, Electronic and Catalytic Properties of TiO2-Supported Bimetallic Au-Ag Catalysts in 1-Octanol Selective Oxidation  |f Yu. Kotolevich, E. G. Pakrieva, E. N. Kolobova [et al.] 
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330 |a Au and Ag were deposited on TiO2 modified with Ce, La, Fe or Mg in order to obtain bimetallic catalysts to be used for liquid-phase oxidation of 1-octanol. The effects of the deposition order of gold and silver, and the nature of the support modifying additives and redox pretreatments on the catalytic properties of the bimetallic Au-Ag catalysts were studied. Catalysts were characterized by low-temperature nitrogen adsorption–desorption, energy dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy and ultraviolet-visible diffuse reflectance spectroscopy. It was found that pretreatments with hydrogen and oxygen at 300 °C significantly decreased the activity of AuAg catalysts (silver was deposited first) and had little effect on the catalytic properties of AgAu samples (gold was deposited first). The density functional theory method demonstrated that the adsorption energy of 1-octanol increased for all positively charged AuxAgyq (x + y = 10, with a charge of q = 0 or +1) clusters compared with the neutral counterparts. Lanthanum oxide was a very effective promoter for both monometallic and bimetallic gold and silver catalysts in the studied process. 
461 |t Catalysts 
463 |t Vol. 11, iss. 7  |v [799, 18 p.]  |d 2021 
610 1 |a электронный ресурс 
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610 1 |a bimetallic catalysts 
610 1 |a 1-octanol oxidation 
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610 1 |a биметаллические катализаторы 
610 1 |a окисление 
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701 1 |a Kolobova  |b E. N.  |c Chemical Engineer  |c design engineer of Tomsk Polytechnic University  |f 1989-  |g Ekaterina Nikolaevna  |3 (RuTPU)RU\TPU\pers\34488  |9 17871 
701 1 |a Farias  |b M. H.  |g Mario 
701 1 |a Bogdanchikova  |b N.  |g Nina 
701 1 |a Corberan  |b V. C.  |g Cortes 
701 1 |a Pichugina  |b D. A.  |g Daria 
701 1 |a Nikitina  |b N. A.  |g Nadezhda 
701 1 |a Carabineiro  |b S. A. C.  |g Sonia Alexandra Correia 
701 1 |a Pestryakov  |b A. N.  |c Chemist  |c Professor of Tomsk Polytechnic University, Doctor of Chemical Science  |f 1963-  |g Aleksey Nikolaevich  |3 (RuTPU)RU\TPU\pers\30471  |9 14796 
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