Vapor-phase hydrogenolysis of biomass-derived lactate to 1,2-propanediol over supported metal catalysts

被引:34
作者
Huang, Long [1 ,2 ]
Zhu, Yulei [1 ,3 ]
Zheng, Hongyan [3 ]
Du, Mingxian [1 ]
Li, Yongwang [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100039, Peoples R China
[3] Synfuels CHINA Co Ltd, Taiyuan 030001, Peoples R China
关键词
Ethyl lactate; 1,2-Propendiol; CO/SiO2; Hydrogenolysis;
D O I
10.1016/j.apcata.2008.07.031
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
Vapor-phase hydrogenolysis of ethyl lactate to 1,2-propanediol was performed over a series of SiO2 supported metal (Fe, Co, Ni, Ru, and Pd) catalysts in a fixed-bed reactor. Among them, the Co/SiO2 and Cu/SiO2 catalysts exhibit promising performance, and the Co/SiO2 were more active than the traditional copper Catalysts Under mild conditions. Effects Of Support, metal loading and preparation method were investigated to optimize the performance of the Co-based catalysts. Over the optimal catalyst (a 10 wt.% Co/SiO2 catalyst prepared via rotary evaporation drying method), the 1,2-propanediol selectivity was in excess of 98% at 90.2% lactate conversion, 2.5 MPa and 160 degrees C. The cobalt catalysts were characterized by X-ray diffraction (XRD) and temperature programmed reduction by H-2 (H-2-TPR) and temperature programmed desorption of H-2 (H-2-TPD). Interestingly, a quasi-linear correlation is observed between the average reaction rate and the percentage of bulk-like Co3O4 phase precursors, suggesting that the metallic cobalt from the bulk-like Co3O4 phase precursor is more active than that from the cobalt surface support species. The emerging technologies for production of low-cost lactate ester, make this high-yield route a sustainable benign process for 1,2-propanediol. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:204 / 211
页数:8
相关论文
共 37 条
[1]   Ester hydrogenolysis over promoted Cu/SiO2 catalysts [J].
Brands, DS ;
Poels, EK ;
Bliek, A .
APPLIED CATALYSIS A-GENERAL, 1999, 184 (02) :279-289
[2]   Green chemistry: today (and tomorrow) [J].
Clark, JH .
GREEN CHEMISTRY, 2006, 8 (01) :17-21
[3]   SELECTIVE HYDROGENOLYSIS OF METHYL AND ETHYL-ACETATE IN THE GAS-PHASE ON COPPER AND SUPPORTED GROUP-VIII METAL-CATALYSTS [J].
CLAUS, P ;
LUCAS, M ;
LUCKE, B ;
BERNDT, T ;
BIRKE, P .
APPLIED CATALYSIS, 1991, 79 (01) :1-18
[4]   Chemical routes for the transformation of biomass into chemicals [J].
Corma, Avelino ;
Iborra, Sara ;
Velty, Alexandra .
CHEMICAL REVIEWS, 2007, 107 (06) :2411-2502
[5]   Conversion of biomass to 1,2-propanediol by selective catalytic hydrogenation of lactic acid over silica-supported copper [J].
Cortright, RD ;
Sanchez-Castillo, M ;
Dumesic, JA .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2002, 39 (04) :353-359
[6]  
Cullity B.D., 1956, Elements of X-ray Diffraction, P259
[7]   The role of the titania and silica supports in Ru-Fe catalysts to partial hydrogenation of benzene [J].
da-Silva, JW ;
Cobo, AJG .
APPLIED CATALYSIS A-GENERAL, 2003, 252 (01) :9-16
[8]   Mild electrocatalytic hydrogenation of lactic acid to lactaldehyde and propylene glycol [J].
Dalavoy, Tulika S. ;
Jackson, James E. ;
Swain, Greg M. ;
Miller, Dennis J. ;
Li, Jie ;
Lipkowski, Jacek .
JOURNAL OF CATALYSIS, 2007, 246 (01) :15-28
[9]   Lactic acid: recent advances in products, processes and technologies - a review [J].
Datta, Rathin ;
Henry, Michael .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2006, 81 (07) :1119-1129
[10]   Cobalt dispersion, reducibility, and surface sites in promoted silica-supported Fischer-Tropsch catalysts [J].
Girardon, J.-S. ;
Quinet, E. ;
Griboval-Constant, A. ;
Chernavskii, P. A. ;
Gengembre, L. ;
Khodakov, A. Y. .
JOURNAL OF CATALYSIS, 2007, 248 (02) :143-157