催化作用
二氧化碳重整
材料科学
甲烷
粒径
路易斯酸
化学工程
无机化学
沉积(地质)
碳纤维
合成气
化学
有机化学
复合材料
复合数
古生物学
工程类
沉积物
生物
作者
Jun Ni,Luwei Chen,Jianyi Lin,Sibudjing Kawi
出处
期刊:Nano Energy
[Elsevier BV]
日期:2012-07-25
卷期号:1 (5): 674-686
被引量:186
标识
DOI:10.1016/j.nanoen.2012.07.011
摘要
Abstract Borated alumina supported 5 wt% Ni catalysts with B2O3 loading varying from 0 wt%, 1 wt%, 5 wt% to 10 wt% were prepared and characterized by XRD, H2-TPR, CO2-TPD, NH3-TPD, in situ DRIFTS study, and evaluated for dry reforming of methane. The addition of B2O3 influences the activity and stability of the catalysts significantly. Ni particle size increases from 5.8 to 9.1 nm with increasing the B2O3 loading from 0 to 10 wt%. In the kinetic control temperature region (700 °C) there is no linear relationship between the Ni particle size and the catalyst activity/stability. The formation of strong Lewis acid sites causes severe carbon deposition on 1 wt% and 10 wt% B2O3 loaded Ni catalysts, hence decreasing catalytic activity and stability. The formation of weak Lewis acid sites and O–H groups on 5 wt% B2O3 promoted Ni catalyst is found to significantly facilitate carbon removal and improve the stability of the catalysts. The reaction mechanism of dry reforming of methane over borated-alumina supported Ni catalysts is proposed, especially the promotional effect of OH groups on the suppression of carbon formation being emphasized.
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