Ni/MgO-Al2O3 Catalysts for CO2 Methanation: Deactivation Mechanism Study

被引:0
作者
Xing, Rui [1 ]
Jiang, Yanan [1 ]
Li, Jia [1 ]
Liu, Pengxiang [2 ]
Liu, Yuan [1 ]
Zhang, Cuijuan [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin Key Lab Appl Catalysis Sci & Technol, Tianjin 300350, Peoples R China
[2] China Chem Technol Res Inst, Beijing 102400, Peoples R China
基金
中国国家自然科学基金;
关键词
X-RAY-ABSORPTION; HYDROGEN; SUPPORT; METAL; STATE; COKE; GAS;
D O I
10.1021/acs.iecr.5c01312
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Despite significant advances in catalytic activity for CO2 methanation, the catalyst stability has received less attention, limiting its application. This work prepared Ni-supported on MgO-Al2O3 with varying Mg/Al ratio (x) and studied their deactivation mechanism. The deactivation was accelerated by a stability test at 600 degrees C for 200 h. The activity comparison before and after the stability test reveals that the sample with x = 0.4 shows the best stability without obvious activity decline. While the sample with x = 0.3 is deactivated due to Ni sintering, samples with x = 0.5 and 0.6 are deactivated by the oxidation of Ni, which easily forms a solid solution with excess MgO but is difficult to reduce. That assertion is supported by various characterizations. Such an oxidative deactivation is first-time reported for Ni-based catalysts for CO2 methanation, which could shed light on their rational design and industrial application.
引用
收藏
页码:13653 / 13662
页数:10
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