催化作用
双金属片
选择性
环氧丙烷
丙烯醛
材料科学
金属
无机化学
化学
有机化学
冶金
共聚物
复合材料
聚合物
环氧乙烷
作者
Xiang Zheng,Yanglong Guo,Yun Guo,Qing Zhang,Xiaohui Liu,Li Wang,Wangcheng Zhan,Guanzhong Lu
出处
期刊:Rare Metals
[Springer Nature]
日期:2015-05-26
卷期号:34 (7): 477-490
被引量:34
标识
DOI:10.1007/s12598-015-0500-y
摘要
Abstract The unsupported Cu and Ag catalysts with different oxidation states were prepared, and their catalytic performances for propylene epoxidation were investigated. The metallic Cu catalyst exhibits much higher catalytic activity and propylene oxide (PO) selectivity than Cu 2 O and CuO catalysts. The Cu 0 species are the main active sites for propylene epoxidation, but Cu 2 O and CuO species are in favor of CO 2 and acrolein production. The PO selectivity of 54.2 % and propylene conversion of 2.6 % can be achieved over the metallic Cu catalyst at 160 °C in initial stage, but metallic Cu catalyst would be oxidized to Cu 2 O during propylene epoxidation, resulting in a sharp decrease in the PO selectivity and propylene conversion. Nanosize AgCu x bimetallic catalysts were prepared. It is found that adding Ag to the metallic Cu catalysts can prevent the oxidation of Cu and make AgCu x bimetallic catalysts more stable under the condition of propylene epoxidation. The Ag/Cu molar ratio can remarkably affect the catalytic performance of AgCu x catalyst and the selectivity to PO and acrolein. After AgCu x was supported on MO x ‐modified α‐Al 2 O 3 , its catalytic performance can be improved and has a close relationship with the acid–base property of support.
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