Active species of copper chromite catalyst in C-O hydrogenolysis of 5-methylfurfuryl alcohol

被引:155
作者
Deutsch, Keenan L. [1 ]
Shanks, Brent H. [1 ]
机构
[1] Iowa State Univ, Dept Chem & Biol Engn, Ames, IA 50011 USA
基金
美国国家科学基金会;
关键词
Hydrogenolysis; Copper catalyst; Copper chromite; 5-Hydroxymethylfurfural; 2,5-Dimethylfuran; Deoxygenation; Biorenewables; VAPOR-PHASE HYDROGENATION; FURFURYL ALCOHOL; SELECTIVE HYDROGENATION; KINETICS; METHANOL; 2-METHYLFURAN; REDUCTION; OXIDE;
D O I
10.1016/j.jcat.2011.09.030
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The active sites of copper chromite catalyst, CuCr2O4 center dot CuO, were investigated for the condensed-phase hydrogenolysis of 5-methylfurfuryl alcohol to 2,5-dimethylfuran at 220 degrees C. The bulk and surface features of the catalyst were characterized by XRD, H-2-TPR, N-2 adsorption, CO chemisorption, N2O titration, NH3-TPD, XPS, and AES. Maxima of both of the potential active species, Cu-0 and Cu+, occurred after reduction in H-2 at 300 degrees C compared to 240 and 360 degrees C. These Cu-0 and Cu+ maxima also coincided with the highest specific rate of reaction based on the surface area of the reduced catalyst. The trends of Cu-0 and Cu+ observed by N2O titration and CO chemisorption were also observed qualitatively by AES. Correlations between activity and the possible active species suggested that Cu-0 was primarily responsible for the activity of the catalysts. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:235 / 241
页数:7
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