非阻塞I/O
煅烧
催化作用
二氧化碳重整
色散(光学)
化学工程
甲烷
合成气
材料科学
镍
化学
冶金
有机化学
光学
物理
工程类
作者
Liying Shi,Yu‐Xia Li,Ding‐Ming Xue,Peng Tan,Yao Jiang,Xiao‐Qin Liu,Lin‐Bing Sun
标识
DOI:10.1016/j.cej.2020.124491
摘要
The dry reforming of CH4 (DRM) with CO2 has received much attention due to the utilization of two green-house gases for the production of syngas. Nickel-containing catalysts have been applied widely in DRM due to their considerable catalytic activity and relative affordable cost, and the activity of catalysts relies on the dispersion of Ni species. Here we developed a nanoconfinement strategy to facilitate the dispersion of NiO in nanoconfined spaces provided by as-made SBA-15 (AS) occluded with the template. The Ni precursor can be inserted into the nanoconfined spaces between silica walls and template in AS by grinding, and in subsequent calcination for NiO formation, aggregation that takes place in conventional calcined SBA-15 (CS) without template can be effectively avoided. Our results show that a high amount of NiO (4 mmol/g, 23 wt%) can be well dispersed in the material from AS (denoted as NiAS), while serious aggregation occurs for the material from CS with the same NiO loading (denoted as NiCS). We also demonstrate that NiAS samples exhibit distinctively higher catalytic activity in DRM with CO2 compared with their NiCS analogues. For the typical 3NiAS catalyst containing 3 mmol/g NiO, the conversions of CO2 and CH4 are 64.2% and 53.7% at 750 °C respectively, which are evidently higher than that of CO2 (40.7%) and CH4 (29.0%) over 3NiCS. Furthermore, the NiAS materials present good coking-resistance, while their NiCS counterparts suffer from serious coking.
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