甲烷
二氧化碳重整
催化作用
环境科学
硫黄
分离(统计)
温室气体
化学
化学工程
环境化学
废物管理
材料科学
地质学
计算机科学
合成气
有机化学
工程类
海洋学
机器学习
作者
Dekang Li,Zhixian Bao,Lijun Jin,Haoquan Hu
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-09-02
卷期号:39 (36): 17258-17268
被引量:2
标识
DOI:10.1021/acs.energyfuels.5c02732
摘要
Dry reforming of methane (DRM) can spontaneously use CO 2 and CH 4 to produce syngas, but minimal sulfur impurities in the feed gas can poison and deactivate the catalyst. Although the Ni/Al 2 O 3 catalyst has excellent DRM activity, it is challenging to regenerate due to sulfation of the support. Besides that, the loading of sacrificial promoters used to improve sulfur resistance, such as Cu, may impact the DRM performance of active sites. Here, a spatial separation strategy was proposed to precisely design a sulfur-resistant catalyst, dividing the catalyst into a DRM zone and a H 2 S adsorption zone. The Ni@SiO 2 @NiCu catalyst prepared by this strategy shows stable DRM performance and significantly improved sulfur resistance and can be regenerated repeatedly. The Ni@SiO 2 @NiCu catalyst has the best sulfur resistance, 6.8 times that of the spatially adjacent NiCu@SiO 2 catalyst and 1.4 times that of the Ni@SiO 2 @Cu catalyst. This spatial separation strategy introduces a novel concept for the controllable synthesis of sulfur-resistant catalysts and may inspire further applications in the design and development of such catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI