煅烧
催化作用
氨
无机化学
解吸
相(物质)
氧化物
材料科学
金属
化学工程
氧化铝
钌
化学
吸附
有机化学
冶金
工程类
作者
Bingyu Lin,Lan Heng,Biyun Fang,Haiyun Yin,Jun Ni,Xiuyun Wang,Jianxin Lin,Lilong Jiang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2019-01-15
卷期号:9 (3): 1635-1644
被引量:148
标识
DOI:10.1021/acscatal.8b03554
摘要
The increase of alumina calcination temperature from 800 °C to 1300 °C results in the transformation of γ-Al2O3 to α-Al2O3 phase accompanying a decrease of specific surface area and the amount of tetrahedral Al3+ sites. Over Ru–Ba/alumina catalysts, an increase in alumina calcination temperature would broaden the size distribution of Ru particles, enlarge the metal-to-oxide ratio of Ru, decrease the amount of surface hydroxyl groups, as well as lower the temperature for N2 desorption. As a result, the increase of alumina calcination temperature lessens the effect of hydrogen poisoning and decreases the activation energy for ammonia synthesis. The Ru–Ba/Al2O3 catalyst with alumina calcined at 980 °C having both θ-Al2O3 and α-Al2O3 shows ammonia synthesis rate three times higher than that with alumina calcined at 800 °C having a γ-Al2O3 phase.
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