催化作用
空间速度
化学工程
材料科学
部分氧化
氧化物
合成气
氢
弹丸
图层(电子)
化学
复合材料
冶金
选择性
有机化学
工程类
作者
Tae Ho Lee,Un Ho Jung,Hyo Been Im,Kyoung Deok Kim,Jiyu Kim,Young Eun Kim,Dahye Song,Kee Young Koo
标识
DOI:10.1016/j.jiec.2022.02.050
摘要
The catalytic activity of structured catalysts comprising Fecralloy and SiC monoliths coated with Ru/Mg-Al oxide by deposition–precipitation was evaluated in the partial oxidation of natural gas and compared with that of a conventional pellet catalyst. The geometric surface area (GSA) of the Fecralloy and SiC monolithic catalysts were 377.0 × 10-4 and 118.5 × 10-4 m2, respectively; significantly larger than that of the 0.5% Ru/Al2O3 pellet catalyst (89.6 × 10-4 m2). Owing to the high GSA of the structured catalysts, a small amount of Ru (0.070–0.12 wt%) resulted in highly dispersed uniform loading. Thus, the structured catalysts exhibited higher performance for catalytic partial oxidation at varying C/O2 ratio, inlet temperature, and gas hourly space velocity (GHSV) than the pellet catalyst. However, in a stability test at high GHSV (50,000 h−1), the CH4 conversion of the Fecralloy monolithic catalyst decreased rapidly from 90% to less than 70% in 150 min. In addition, the Mg-Al oxide layer of the Fecralloy monolithic catalyst was damaged owing to material deterioration, resulting in a loss of Ru particles. In contrast, CH4 conversion catalyzed by the SiC monolithic catalysts remained above 85% even after 1000 min, and the material or support layer was not damaged even under severe conditions.
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