焦炭
催化作用
化学工程
材料科学
烧结
tar(计算)
甲苯
介孔材料
催化裂化
冶金
化学
有机化学
计算机科学
工程类
程序设计语言
作者
Ye Tian,Xiaoqian Ma,Xinfei Chen,Zhang Chaoyue,Xiaoluan Lu
标识
DOI:10.1016/j.ijhydene.2022.02.130
摘要
The development of catalysts with resistance to sintering and coke deposition is the key to tar cracking during biomass gasification technology. In this work, the core-shell catalysts with mesoporous and microporous silica-coated nickel nanoparticles were prepared for the CO2 reforming of toluene as a model compound for biomass tar. The influence of thickness of SiO2 shell layer on catalyst activity, coke and sintering resistance of the catalysts in the CO2 reforming of toluene was explored. Appropriate increasing in the thickness of the silica shell can significantly increase the specific surface area, pore volume and the interaction between core and shell of the catalysts, which can further improve the reactivity and coke resistance ability. However, excessive increase in shell thickness can lead to a drastic decrease in the specific surface area and pore volume of the catalyst, resulting in significant coke deposition. The [email protected]2-4 catalyst showed the highest catalytic activity of toluene conversion of around 50% within 300 min, stability H2/CO ratio of 0.25∼0.3 and durability of 26 h lifetime in the CO2 reforming of toluene. Overall, the optimization of the silica shell thickness can improve the reactivity and coke resistance ability of [email protected]2.
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