A Comparative Study of Hydroxyapatite- and Alumina-Based Catalysts in Dry Reforming of Methane

被引:10
作者
Rego de Vasconcelos, Bruna [1 ,2 ]
Pham Minh, Doan [1 ,3 ]
Martins, Emmanuel [4 ]
Germeau, Alain [4 ]
Sharrock, Patrick [1 ]
Nzihou, Ange [1 ]
机构
[1] Univ Toulouse, IMT Mines Albi, UMR 5302, CNRS,Ctr RAPSODEE, Campus Jarlard, F-81013 Albi 09, France
[2] Univ Sherbrooke, Biomass Technol Lab, Dept Chem & Biotechnol Engn, Sherbrooke, PQ J1K 2R1, Canada
[3] Duy Tan Univ, Inst Res & Dev, Da Nang 550000, Vietnam
[4] PRAYON SA, Rue J Wauters 144, B-4480 Engis, Belgium
关键词
Carbon dioxide; Dry reforming of methane; Hydroxyapatite; Nickel-based catalysts; Simulated industrial conditions; CARBON-DIOXIDE; NI; CO; CE;
D O I
10.1002/ceat.201900461
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The dry reforming of methane over hydroxyapatite- and alumina/magnesia (commercial Pural MG 30)-supported nickel catalysts was investigated. The catalytic performance of the catalysts prepared with fresh supports highly depended on the basicity, the metal-support interaction, and the metal particle size. Calcination of the supports at 1200 degrees C for 5 h made the catalysts less active because of specific surface area reduction and basicity destruction. However, this treatment allowed avoiding any further catalyst deactivation by thermal sintering and maintained excellent catalytic stability over 300 h of time-on-stream. These tests under simulated industrial conditions (high contact time and long time-on-stream) showed the competitiveness of the prepared catalysts in this important catalytic process.
引用
收藏
页码:698 / 704
页数:7
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