催化作用
甲烷
焦炭
合成气
二氧化碳重整
热重分析
化学
分解
碳纤维
程序升温还原
解吸
无机化学
化学工程
材料科学
有机化学
吸附
工程类
复合数
复合材料
作者
Ahmed Yagoub Elnour,Anis H. Fakeeha,Ahmed A. Ibrahim,Ahmed I. Osman,Ahmed E. Abasaeed,Syed Farooq Adil,Rawesh Kumar,Ahmed S. Al‐Fatesh
标识
DOI:10.1007/s11164-023-05210-4
摘要
Abstract The first step of the DRM reaction is just the decomposition of CH 4 into CH 4−x ( x = 1–4). The next step comprises two steps, namely the oxidation of CH 4−x into syngas (by CO 2 ) and the self-polymerization of CH 4−x species. The earlier one is known as dry reforming of methane (DRM), and the latter one generates carbon deposits over the catalyst surface. In this study, we investigated the impact of 1–3 wt% Sr over Ni-based catalysts on a ZrO 2 -WO 3 support on the catalytic activity and coke deposit. Various characterization techniques such as thermogravimetric analysis, X-ray diffraction, Raman spectroscopy, temperature-programed oxidation, temperature-programed reduction, and temperature-programed desorption were used to assess the physicochemical properties of the fresh and spent catalysts. The addition of 2wt% Sr promoter significantly improves the catalyst’s basicity in strong basic sites region through Sr 2+ mediated interaction of CO 2 species as well as inhibits the deposition of carbyne type carbon. Enhanced CO 2 interaction results into the potential oxidation of carbon deposit and the highest CH 4 conversion, reaching 60% up to 470 min TOS at a reaction temperature of 700 ℃. Graphical abstract
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