Effect of redox treatments on activation and deactivation of gold nanospecies supported on mesoporous silica in CO oxidation; Fuel; Vol. 110 : IMCCRE 2012 “International-Mexican Congress on Chemical Reaction Engineering”

Bibliographische Detailangaben
Parent link:Fuel
Vol. 110 : IMCCRE 2012 “International-Mexican Congress on Chemical Reaction Engineering”.— 2013.— [P. 40-47]
Weitere Verfasser: Bogdanchikova N., Pestryakov A. N. Aleksey Nikolaevich, Tuzovskaya I., Zepeda T. A., Farias M. H., Tiznado H., Martynyuk O. A. Oksana Anatolievna
Zusammenfassung:Title screen
The influence of pretreatments with He, O2 and H2 on the physicochemical and catalytic properties of gold supported on hexagonal mesoporous silica (HMS) has been studied by a variety of methods including: XPS, TPR, N2 sorption, UV-visible spectroscopy, FTIR and catalytic testing. The investigations show supported gold to form different states under redox treatments: Au3+ and Au+ ions, neutral and partly charged gold clusters and metal nanoparticles of different sizes. Reducing pretreatments increase the catalytic activity of the samples; while oxidative treatments deactivate the catalyst. Catalytic tests show several regions of the reduced samples with various catalytic behaviours: 20-200 °C, 200-400 °C and >400 °C; this situation is explained by the co-existence of gold active sites of different types. A comparative analysis among spectroscopic and catalytic data allows suggesting clusters to be responsible for the activity in the low-temperature region (<200 °C); neutral Aun clusters are active in the range 200-400 °C; and gold nanoparticles may catalyze high-temperature CO oxidation. Au3+ ions are inactive in this process.
Режим доступа: по договору с организацией-держателем ресурса
Sprache:Englisch
Veröffentlicht: 2013
Schlagworte:
Online-Zugang:http://dx.doi.org/10.1016/j.fuel.2012.09.064
Format: Elektronisch Buchkapitel
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=636298

MARC

LEADER 00000nla0a2200000 4500
001 636298
005 20250321150454.0
035 |a (RuTPU)RU\TPU\network\194 
035 |a RU\TPU\network\79 
090 |a 636298 
100 |a 20131112d2013 k||y0rusy50 ba 
101 0 |a eng 
135 |a drnn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Effect of redox treatments on activation and deactivation of gold nanospecies supported on mesoporous silica in CO oxidation  |f N. Bogdanchikova [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: p. 46-47 (70 tit.)] 
330 |a The influence of pretreatments with He, O2 and H2 on the physicochemical and catalytic properties of gold supported on hexagonal mesoporous silica (HMS) has been studied by a variety of methods including: XPS, TPR, N2 sorption, UV-visible spectroscopy, FTIR and catalytic testing. The investigations show supported gold to form different states under redox treatments: Au3+ and Au+ ions, neutral and partly charged gold clusters and metal nanoparticles of different sizes. Reducing pretreatments increase the catalytic activity of the samples; while oxidative treatments deactivate the catalyst. Catalytic tests show several regions of the reduced samples with various catalytic behaviours: 20-200 °C, 200-400 °C and >400 °C; this situation is explained by the co-existence of gold active sites of different types. A comparative analysis among spectroscopic and catalytic data allows suggesting clusters to be responsible for the activity in the low-temperature region (<200 °C); neutral Aun clusters are active in the range 200-400 °C; and gold nanoparticles may catalyze high-temperature CO oxidation. Au3+ ions are inactive in this process. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Fuel 
463 |t Vol. 110 : IMCCRE 2012 “International-Mexican Congress on Chemical Reaction Engineering”  |v [P. 40-47]  |d 2013 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a gold 
610 1 |a золото 
610 1 |a silica 
610 1 |a кремнеземы 
610 1 |a oxidation 
610 1 |a окисление 
610 1 |a clusters 
610 1 |a кластеры 
610 1 |a nanoparticles 
610 1 |a наночастицы 
701 1 |a Bogdanchikova  |b N. 
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 
701 1 |a Tuzovskaya  |b I. 
701 1 |a Zepeda  |b T. A. 
701 1 |a Farias  |b M. H. 
701 1 |a Tiznado  |b H. 
701 1 |a Martynyuk  |b O. A.  |c chemist  |c Researcher of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1982-  |g Oksana Anatolievna  |3 (RuTPU)RU\TPU\pers\31284  |9 15462 
801 2 |a RU  |b 63413507  |c 20151224  |g RCR 
856 4 |u http://dx.doi.org/10.1016/j.fuel.2012.09.064 
942 |c CF