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Selective Oxidation of Glycerol over Platinum-Based Catalysts Supported on Carbon Nanotubes
被引:34
作者:

Rodrigues, Elodie G.
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Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal

Pereira, Manuel F. R.
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Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal

Chen, Xiaowei
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机构:
Univ Cadiz, Dept Ciencia Mat & Ingn Met & Quim Inorgan, Fac Ciencias, Cadiz 11510, Spain Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal

Delgado, Juan J.
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机构:
Univ Cadiz, Dept Ciencia Mat & Ingn Met & Quim Inorgan, Fac Ciencias, Cadiz 11510, Spain Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal

Orfao, Jose J. M.
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Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal
机构:
[1] Univ Porto, LCM, Lab Associado LSRE LCM, Dept Engn Quim,Fac Engn, P-4200465 Oporto, Portugal
[2] Univ Cadiz, Dept Ciencia Mat & Ingn Met & Quim Inorgan, Fac Ciencias, Cadiz 11510, Spain
关键词:
LIQUID-PHASE OXIDATION;
FREE AQUEOUS-SOLUTION;
BIMETALLIC CATALYSTS;
METAL-CATALYSTS;
MOLECULAR-OXYGEN;
GOLD CATALYSTS;
PD;
NANOPARTICLES;
AU;
CHEMICALS;
D O I:
10.1021/ie402331u
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
Platinum was supported on multiwalled carbon nanotubes by the traditional incipient wetness impregnation and tested in the selective oxidation of glycerol. This catalyst is prone to deactivation possibly by oxygen poisoning. A platinum catalyst prepared by the sol immobilization technique is less susceptible to deactivation, probably due to the higher average size of the particles obtained; in addition a high and stable selectivity toward glyceric acid was observed throughout the reaction (67%). Tests with a Pt-Au bimetallic catalyst under high pH conditions show that deactivation is suppressed. Moreover, this catalyst is able to enhance the selectivity toward dihydroxyacetone (DIHA) in acid medium, when compared to a monometallic platinum catalyst with the same total metal loading (21% vs 13%), although a poorer performance had been obtained.
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页码:17390 / 17398
页数:9
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