催化作用
钴
碳纤维
甲烷
水煤气变换反应
溶剂
化学
材料科学
二氧化碳
化学工程
二氧化碳重整
无机化学
合成气
有机化学
复合数
工程类
复合材料
作者
My Hien Thi Bach,Ngoc Thang Tran,Thanh Nha Thi Tran,Van Cuong Nguyen,Thi Hong Anh Nguyen
摘要
This study aimed to synthesize alumina from an inorganic aluminum nitrate precursor in various binary solvent systems of ethanol and water using the sol-gel self-assembly (SSA) method, employing a triblock copolymer, pluronic P123, as the pore-directing agent. The resulting materials were implemented as a support for the cobalt (Co) catalyst in a methane dry reforming (MDR) reaction at 1073 K under 1 atm. Regardless of the water percentage used in the support synthesis, the methane dry reforming reaction over Co catalysts on alumina supports showed the negligible change in conversion during the 12 h reaction. Moreover, there was evidence of large quantities of amorphous carbon and graphitic carbon on the spent catalyst surface. However, the low oxidation temperature of these deposited carbons could help maintain the balance between the carbon formation and the carbon elimination processes on the catalyst surface during the reforming reaction, hence prolonging the lifetime of the catalyst. The high conversion of methane (CH4) from 64.6% to 82.8% and carbon dioxide (CO2) from 70.7% to 86.6% for the MDR reaction over the as-prepared alumina-supported Co catalyst demonstrated a significant improvement in catalyst production for the MDR reaction from the viewpoint of large-scale applications.
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