Tuning the composition of metastable COxNiyMg100-x-y(OH)(OCH3) nanoplates for optimizing robust methane dry reforming catalyst

被引:74
作者
Fan, Xiaoli [1 ]
Liu, Zhiting [1 ]
Zhu, Yi-An [1 ]
Tong, Gangsheng [2 ]
Zhang, Jingdong [3 ]
Engelbrekt, Christian [3 ]
Ulstrup, Jens [3 ]
Zhu, Kake [1 ]
Zhou, Xinggui [1 ]
机构
[1] E China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, UNILAB, Shanghai 200237, Peoples R China
[2] Shanghai Jiao Tong Univ, Instrumental Anal Ctr, Shanghai 200240, Peoples R China
[3] Tech Univ Denmark, Dept Chem, DK-2800 Lyngby, Denmark
基金
中国国家自然科学基金;
关键词
Methane; Carbon dioxide; Reforming; Reaction kinetics; Coke deposition; Cobalt; Nickel; Solvothermal synthesis; SOLID-SOLUTION CATALYSTS; SUPPORTED NI CATALYSTS; NICKEL BIMETALLIC CATALYSTS; CARBON-DIOXIDE; SYNGAS PRODUCTION; SYNTHESIS GAS; SURFACE CARBON; CO2; CH4; MGO;
D O I
10.1016/j.jcat.2015.06.018
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
Finding controllable, low-cost, and scalable ways to generate Ni-based catalysts is the bottleneck for methane dry reforming catalyst design. A new method for generating trimetallic CoxNiyMg100-x-yO solid solution platelets enclosed by (111) facets has been developed from the topotactic pyrolysis of the metastable precursor CoxNiyMg100-x-y(OH)(OCH3) derived from solvothermal synthesis. The catalyst composition and reaction conditions have been modulated to achieve maximum coke resistance and catalyst stability. Long-term stability for 1000 h time on stream at 800 degrees C has been achieved for the optimized Co0.075Ni7.425Mg92.5O catalyst. The role of Co in the catalyst has been disclosed through kinetic measurements and detailed characterization of the spent catalysts. Co is enriched on the Co-Ni alloy surface under reforming conditions and accelerates the gasification of coke intermediates. Co also enhances the chemisorption of oxygen and reduces the activation energy for methane fragmentation, which is the rate-determining step for the overall reaction. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:106 / 119
页数:14
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