甲烷化
催化作用
合成气
尖晶石
反应性(心理学)
化学工程
材料科学
烧结
镍
热稳定性
无机化学
化学
冶金
有机化学
替代医学
病理
工程类
医学
作者
Gengrui Zhang,Yan Li,Yong Chen,Hao Xinning,Xianhua Zhang,Shuai Wang,Jingdong Lin,Yong Wang,Shaolong Wan
标识
DOI:10.1021/acs.iecr.3c02097
摘要
The development of Ni-based syngas methanation catalysts with superior thermal stability remains a formidable challenge, which typically requires the use of a high Ni loading and a recipe containing very complex components. Herein, a novel Ni catalyst using a ZnAl 2 O 4 spinel support was designed and prepared by an isopropanol-mediated controlled hydrolysis method, which demonstrated excellent reactivity and stability toward the syngas methanation reaction. Moreover, the 35% Ni/ZnAl 2 O 4 catalyst still maintained a high reactivity after steam treatment at 750 °C, while the 35% Ni/Al 2 O 3 counterpart suffered a nearly complete loss of reactivity during such an accelerated test. The detailed characterization reveals that the drastic deactivation of Ni/Al 2 O 3 after steam treatment is attributed to the favored formation of NiAl 2 O 4 under the severe reaction atmosphere, resulting in the loss of active Ni. In contrast, the employment of the highly stable ZnAl 2 O 4 support can not only inhibit the sintering of supported Ni particles due to their strong interaction but also avoid the loss of the active Ni component by preventing the formation of NiAl 2 O 4 . This work sheds light on the critical role and the intrinsic mechanism of the spinel support for the construction of the desired methanation catalysts. The mechanistic scenario revealed in this work provides an important and novel solution to overcome the deactivation problem not only useful for methanation catalysts but also valid for most other supported metal catalysts commonly used in the reaction processes that require severe reaction conditions.
科研通智能强力驱动
Strongly Powered by AbleSci AI