水滑石
甲烷化
选择性
催化作用
空间速度
层状双氢氧化物
纳米颗粒
氧化物
多相催化
化学工程
化学
无机化学
材料科学
煅烧
有机化学
纳米技术
工程类
作者
Fabrizio Cavani,Ferruccio Trifirò,Angelo Vaccari
出处
期刊:Catalysis Today
[Elsevier]
日期:1991-12-01
卷期号:11 (2): 173-301
被引量:5352
标识
DOI:10.1016/0920-5861(91)80068-k
摘要
The hydrogenation of CO2 over Ru catalysts is structure sensitive, the selectivity of the process can be driven either to the production of CH4 or CO depending on Ru particles and support features. Herein, Ru-based MgAl-HT (HT=hydrotalcite) derived catalysts with different Ru loadings (0.5, 1.0 and 2.0 wt%) and promoted with La3+ were prepared, characterized, and tested for CO2 methanation at high Gas Hourly Space Velocity values (480 L/gcat h) feeding a CO2/H2/N2 = 1/4/1 v/v mixture. The MgAlOx mixed oxide obtained after calcination at 600 °C and reduction provided weak, medium and mainly strong basic sites, able to activate the CO2 molecule, and hosted very small Ru nanoparticles (1–3 nm). However, the catalysts displayed a low activity in the low temperature range and a poor selectivity to CH4. The addition of La3+, despite contributing to the basicity, did not have any significant effect on performance. In a comparison between Ru- and Ni-HT-derived catalysts, tested under similar reaction conditions, Ni largely overperformed Ru.
科研通智能强力驱动
Strongly Powered by AbleSci AI