In situ time-resolved characterization of novel Cu-MoO2 catalysts during the water-gas shift reaction

被引:31
作者
Wen, Wen
Jing, Liu
White, Michael G.
Marinkovic, Nebojsa
Hanson, Jonathan C.
Rodriguez, Jose A. [1 ]
机构
[1] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[2] Univ Delaware, Dept Chem Engn, Newark, DE 19716 USA
关键词
water-gas shift; copper; molybdenum oxides; CuMoO4; H2; water; CO; CO2; X-ray diffraction; X-ray absorption; spectroscopy;
D O I
10.1007/s10562-006-9003-7
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
A novel and active Cu-MoO2 catalyst was synthesized by partial reduction of a precursor CuMoO4 mixed-metal oxide with CO or H-2 at 200-250 degrees C. The phase transformations of Cu-MoO2 during H-2 reduction and the water-gas shift reaction could be followed by in situ time resolved XRD techniques. During the reduction process the diffraction pattern of the CuMoO4 collapsed and the copper metal lines were observed on an amorphous material background that was assigned to molybdenum oxides. During the first pass of water-gas shift (WGS) reaction, diffraction lines for Cu6Mo5O18 and MoO2 appeared around 350 degrees C and Cu6Mo5O18 was further transformed to Cu/MoO2 at higher temperature. During subsequent passes, significant WGS catalytic activity was observed with relatively stable plateaus in product formation around 350, 400 and 500 degrees C. The interfacial interactions between Cu clusters and MoO2 increased the water-gas shift catalytic activities at 350 and 400 degrees C.
引用
收藏
页码:1 / 6
页数:6
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