A molecular insight into propylene epoxidation on Cu/SiO2 catalysts using O2 as oxidant

被引:106
|
作者
Su, Weiguang [1 ]
Wang, Shouguo [1 ]
Ying, Pinliang [1 ]
Feng, Zhaochi [1 ]
Li, Can [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
C3H6; epoxidation; Cu/SiO2; Propylene oxide; IR spectroscopy; Cu-0 or Cu+ species; Potassium acetate (KAc) modification; VAPOR-PHASE EPOXIDATION; GOLD NANOPARTICLES; IR SPECTROSCOPY; HIGHER OLEFINS; NITROUS-OXIDE; PROPENE OXIDE; CU+ IONS; OXYGEN; HYDROGEN; COPPER;
D O I
10.1016/j.jcat.2009.09.017
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We investigated the catalytic performances of Cu/SiO2 with various promoters on the epoxidation of C3H6 by O-2. Propylene oxide (PO) is the only product at reaction temperatures below 500 K and the rate of PO formation can reach 2.5 mmol g(-1) h(-1) over the potassium acetate (KAc)-Cu/SiO2 Catalyst. IR studies show that both Cu-0 and Cu+ in Cu/SiO2 can activate the C=C bond Of C3H6, and pi donation of C3H6 to Cu-0 or Cu+ also results in a red shift of v(CO) with respect to CO adsorbed on Cu-0 or Cu+ "solo". However, C3H6 is only weakly adsorbed on Cu2+. Both Cu-0 and Cu+ species show C3H6 epoxidation activity. It is proposed that the isolated Cu species and small CuOx clusters with low valence state (Cu-0 or Cu+) modified by KAc are the main active sites for C3H6 epoxidation on Cu/SiO2 catalyst with O-2 as the oxidant. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:165 / 174
页数:10
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