Role of acid sites and selectivity correlation in solvent free liquid phase dehydration of sorbitol to isosorbide

被引:73
作者
Dabbawala, Aasif A. [1 ]
Mishra, Dinesh K. [1 ]
Huber, George W. [2 ]
Hwang, Jin-Soo [1 ]
机构
[1] Korea Res Inst Chem Technol, Biorefinery Res Ctr, Taejon 305600, South Korea
[2] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA
关键词
Dehydration; Sorbitol; Selectivity; Bronsted acid; Lewis acid; CATALYTIC-ACTIVITY; CONVERSION; CELLULOSE; BIOMASS; PHOSPHATE; FRUCTOSE; GLUCOSE; HYDROLYSIS; CHEMICALS; TITANIA;
D O I
10.1016/j.apcata.2014.12.014
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
A number of Bronsted acids (methanesulfonic acid, p-toluene sulfonic acid, triflic acid, sulfamic acid, citric acid, NaHSO4, and boric acid) and Lewis acids (metal sulfate/triflates) were employed in solvent free dehydration of sorbitol and their influence on anhydroalcohols selectivity has been investigated. The outcome indicated that all the acid catalysts produced first mono-dehydrated product sorbitan followed by second dehydration of 1,4-sorbitan to isosorbide. However, the formation and yield isosorbide were found to depend on the nature of acid sites and their acidic strength. The Bronsted acids are more efficient to convert sorbitol to isosorbide than Lewis acids. The Bronsted acids having lower pK(a) value (i.e. strong acid) exhibited high catalytic activity as well as yield of isosorbide. In the case of Lewis acids, the catalytic activity and selectivity were radically depended on which metal used and their stability during the reaction. The water formed during reaction induced Bronsted acidity on Lewis acid metal site. The Lewis-assisted Bronsted acid site enabled high yield of isosorbide up to 70% at moderate temperature (160 degrees C). (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:252 / 261
页数:10
相关论文
共 57 条
[1]  
Abraham T.W., 2012, WO Patent, Patent No. 2012083149
[2]   Liquid-phase dehydration of sorbitol to isosorbide using sulfated titania as a solid acid catalyst [J].
Ahmed, Imteaz ;
Khan, Nazmul Abedin ;
Mishra, Dinesh Kumar ;
Lee, Ji Sun ;
Hwang, Jin-Soo ;
Jhung, Sung Hwa .
CHEMICAL ENGINEERING SCIENCE, 2013, 93 :91-95
[3]  
Andrews M.A., 2001, [No title captured], Patent No. [W0 2001092266 A2, 2001092266]
[4]   Sorbitol Hydrogenolysis Over Ni, Pt and Ru Supported on NaY [J].
Banu, M. ;
Venuvanalingam, P. ;
Shanmugam, R. ;
Viswanathan, B. ;
Sivasanker, S. .
TOPICS IN CATALYSIS, 2012, 55 (11-13) :897-907
[5]  
Beeck B. O., 2013, CHEMSUSCHEM, V6, P199
[6]   Metal triflates: On the question of Lewis versus Bronsted acidity in retinyl carbocation formation [J].
Bradley, D. ;
Williams, G. ;
Lawton, Michelle .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2010, 317 (1-2) :68-71
[7]   Conversion of Cellulose and Cellobiose into Sorbitol Catalyzed by Ruthenium Supported on a Polyoxometalate/Metal-Organic Framework Hybrid [J].
Chen, Jinzhu ;
Wang, Shengpei ;
Huang, Jing ;
Chen, Limin ;
Ma, Longlong ;
Huang, Xing .
CHEMSUSCHEM, 2013, 6 (08) :1545-1555
[8]   Liquid-phase catalytic processing of biomass-derived oxygenated hydrocarbons to fuels and chemicals [J].
Chheda, Juben N. ;
Huber, George W. ;
Dumesic, James A. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (38) :7164-7183
[9]   Conversion of biomass platform molecules into fuel additives and liquid hydrocarbon fuels [J].
Climent, Maria J. ;
Corma, Avelino ;
Iborra, Sara .
GREEN CHEMISTRY, 2014, 16 (02) :516-547
[10]   Chemical routes for the transformation of biomass into chemicals [J].
Corma, Avelino ;
Iborra, Sara ;
Velty, Alexandra .
CHEMICAL REVIEWS, 2007, 107 (06) :2411-2502