甲烷化
催化作用
煅烧
碳纤维
材料科学
硼
化学工程
无定形碳
微晶
多相催化
无机化学
无定形固体
化学
冶金
有机化学
复合材料
复合数
工程类
作者
Anastasios Kambolis,Davide Ferri,Ye Lu,S. N. Yannopoulos,Simone Pokrant,Daniel Rentsch,Oliver Kröcher
出处
期刊:Chemcatchem
[Wiley]
日期:2015-09-03
卷期号:7 (20): 3261-3265
被引量:13
标识
DOI:10.1002/cctc.201500567
摘要
Abstract Carbon deposition during CO methanation from biomass‐derived gas is a significant challenge in terms of catalyst lifetime. It results from the severe reaction conditions imposed by the presence of unsaturated hydrocarbons in the gasified feedstock. This work investigated the structure of boron‐modified Ni/Al 2 O 3 catalysts exhibiting enhanced carbon resistance. As a consequence of B promoting the growth of Ni crystallites, the structure of the B‐modified catalyst was demonstrated to be different at the nanoscale, especially after calcination. The modified catalyst possesses larger Ni particles with porous regions in which B is present. The absence of carbidic and amorphous carbon species, which are considered critical for catalyst deactivation in low‐temperature processes, confirms that B effectively prevents carbon diffusion into Ni, which thus enhances the durability of the catalyst for CO methanation. These results may reveal a strategy of wider significance for developing catalysts with improved stability.
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