糠醇
糠醛
催化作用
空间速度
化学
共沉淀
选择性
X射线光电子能谱
无机化学
核化学
化学工程
有机化学
工程类
作者
Bhari Mallanna Nagaraja,A.H. Padmasri,B. David Raju,Seetha Rama Rao Kamaraju
出处
期刊:Journal of Molecular Catalysis A-chemical
[Elsevier]
日期:2006-09-25
卷期号:265 (1-2): 90-97
被引量:260
标识
DOI:10.1016/j.molcata.2006.09.037
摘要
Cu–MgO catalysts have been employed for the catalytic vapor phase hydrogenation of furfural (FAL) to furfuryl alcohol (FOL) at atmospheric pressure, H2/furfural (molar ratio) = 2.5 and the gas hourly space velocity (GHSV) has been maintained at 0.05 mol h−1 g cat−1. Cu–MgO catalysts with variable Cu loadings (5.2–79.8 wt.%) are prepared by coprecipitation method and are characterized by BET surface area, AAS (atomic adsorption spectroscopy), XRD, XPS and DTA/TGA. Hydrogenation activities of the catalysts, reduced at 523 K in H2 flow for 4 h prior to the reaction are studied in the temperature range of 453–523 K. Cu–MgO catalyst with 16 wt.% of Cu showed hydrogenation activity with 98% conversion of furfural producing furfuryl alcohol with a higher selectivity of 98%. XPS analysis showed the presence of Cu0/Cu+ sites on the catalyst surface that may be responsible for the higher activity compared to other Cu–MgO catalysts studied. The turnover frequency of furfural conversion in the catalysts containing lower composition of Cu is very high. However, due to the lack of required number of Cu0 particles and the absence of Cu+ species in these catalysts, the overall conversion of furfural is low.
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