Carbon deposition on borated alumina supported nano-sized Ni catalysts for dry reforming of CH4

被引:156
作者
Ni, Jun [1 ,3 ]
Chen, Luwei [2 ]
Lin, Jianyi [2 ]
Kawi, Sibudjing [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 119260, Singapore
[2] ASTAR, Inst Chem & Engn Sci, Singapore 627833, Singapore
[3] Zhejiang Univ Technol, Coll Chem Engn & Mat Sci, Inst Ind Catalysis, Hangzhou 310014, Zhejiang, Peoples R China
关键词
Methane reforming; Borated-alumina; Ni catalysts; Acidity/basicity; OH groups; Carbon suppression; BORON-MODIFIED ALUMINA; NICKEL-COPPER ALLOYS; PARTIAL OXIDATION; BORIA CATALYSTS; GAMMA-ALUMINA; SYNTHESIS GAS; METHANE; DIOXIDE; CO2; DEACTIVATION;
D O I
10.1016/j.nanoen.2012.07.011
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
Borated alumina supported 5 wt% Ni catalysts with B2O3 loading varying from 0 wt%, 1 wt%, 5 wt% to 10 wt% were prepared and characterized by XRD, H-2-TPR, CO2-TPD, NH3-TPD, in situ DRIFTS study, and evaluated for dry reforming of methane. The addition of B2O3 influences the activity and stability of the catalysts significantly. Ni particle size increases from 5.8 to 9.1 nm with increasing the B2O3 loading from 0 to 10 wt%. In the kinetic control temperature region (700 degrees C) there is no linear relationship between the Ni particle size and the catalyst activity/stability. The formation of strong Lewis acid sites causes severe carbon deposition on 1 wt% and 10 wt% B2O3 loaded Ni catalysts, hence decreasing catalytic activity and stability. The formation of weak Lewis acid sites and O-H groups on 5 wt% B2O3 promoted Ni catalyst is found to significantly facilitate carbon removal and improve the stability of the catalysts. The reaction mechanism of dry reforming of methane over borated-alumina supported Ni catalysts is proposed, especially the promotional effect of OH groups on the suppression of carbon formation being emphasized. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:674 / 686
页数:13
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