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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.
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页码:165 / 174
页数:10
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