TY - JOUR
T1 - Dimethyl carbonate synthesis from carbon dioxide and methanol over Ni-Cu/MoSiO(VSiO) catalysts
AU - Zhong, S. H.
AU - Wang, J. W.
AU - Xiao, X. F.
AU - Li, H. S.
PY - 2000
Y1 - 2000
N2 - The surface structures, chemisorption properties and catalytic behaviors of Ni-Cu/MoSiO and Ni-Cu/VSiO catalysts have been investigated by using the techniques of XRD, TPR, IR, TPD and micro-reactor. Three types of active sites, metallic site M (Ni-Cu alloy), Lewis acid site Ma+ (Mo6+ or V5+) and Lewis base site M=O (Mo=O or V=O), have been found on the surface of the reduced catalysts. With the cooperation effects of these active sites, CO2 can be chemisorbed on the metallic site M and Lewis acid site Ma+ to form a new type of CO2 horizontal adsorption state, M - (CO) - O→Ma+, and CH3OH can be dissociated on the Lewis base site M=O and Lewis acid site Mn+ to form a dissociative adsorption state, Mn+ - OCH3 and HO - M. The selectivity of dimethyl carbonate synthesized from these adsorption species is over 85% and a surface reaction mechanism of this catalytic reaction is proposed based on the experimental results.
AB - The surface structures, chemisorption properties and catalytic behaviors of Ni-Cu/MoSiO and Ni-Cu/VSiO catalysts have been investigated by using the techniques of XRD, TPR, IR, TPD and micro-reactor. Three types of active sites, metallic site M (Ni-Cu alloy), Lewis acid site Ma+ (Mo6+ or V5+) and Lewis base site M=O (Mo=O or V=O), have been found on the surface of the reduced catalysts. With the cooperation effects of these active sites, CO2 can be chemisorbed on the metallic site M and Lewis acid site Ma+ to form a new type of CO2 horizontal adsorption state, M - (CO) - O→Ma+, and CH3OH can be dissociated on the Lewis base site M=O and Lewis acid site Mn+ to form a dissociative adsorption state, Mn+ - OCH3 and HO - M. The selectivity of dimethyl carbonate synthesized from these adsorption species is over 85% and a surface reaction mechanism of this catalytic reaction is proposed based on the experimental results.
UR - http://www.scopus.com/inward/record.url?scp=0034350649&partnerID=8YFLogxK
U2 - 10.1016/s0167-2991(00)80423-1
DO - 10.1016/s0167-2991(00)80423-1
M3 - Article
AN - SCOPUS:0034350649
SN - 0167-2991
VL - 130 B
SP - 1565
EP - 1570
JO - Studies in Surface Science and Catalysis
JF - Studies in Surface Science and Catalysis
ER -