Conversion of cellobiose into sorbitol in neutral water medium over carbon nanotube-supported ruthenium catalysts

被引:145
作者
Deng, Weiping [1 ]
Liu, Mi [1 ]
Tan, Xuesong [1 ]
Zhang, Qinghong [1 ]
Wang, Ye [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem,State Key Lab Phys Chem Solid Surfaces, Natl Engn Lab Green Chem Prod Alcohols Ethers & E, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomass conversion; Cellobiose; Sorbitol; Ruthenium catalyst; Carbon nanotubes; Hydrogenation; Hydrolysis; OXYGENATED HYDROCARBONS; GLUCOSE HYDROGENATION; CELLULOSE CONVERSION; SYNTHESIS GAS; NANOFIBERS; OXIDATION; CHEMICALS; GROWTH; FUELS; XPS;
D O I
10.1016/j.jcat.2010.01.024
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
Carbon nanotube (CNT)-supported ruthenium catalysts were studied for the hydrogenation of cellobiose in neutral water medium. The acidity of catalysts and the size of Ru particles played key roles in the conversion of cellobiose to sorbitol. A higher concentration of nitric acid used for CNT pretreatment provided a better sorbitol yield, suggesting an important role of catalyst acidity. The catalysts with larger mean sizes of Ru particles and abundant acidic sites exhibited better sorbitol yields, while those with smaller Ru particles and less acidic sites favored the formation of 3-beta-D-glucopyranosyl-D-glucitol. We elucidated that cellobiose was first converted to 3-beta-D-glucopyranosyl-D-glucitol via the hydrogenolysis, and then sorbitol was formed through the cleavage of beta-1,4-glycosidic bond in 3-beta-D-glucopyranosyl-D-glucitol over the catalysts. The catalyst with smaller Ru particles favored the first step but was disadvantageous to the second step due to the less acidity. Smaller Ru particles also accelerated the degradation of sorbitol. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:22 / 32
页数:11
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