Preparation of Cu/SBA-15 catalysts by different methods for the hydrogenolysis of dimethyl maleate to 1,4-butanediol

被引:124
作者
Chen, Liang-Feng
Guo, Ping-Jun
Zhu, Ling-Jun
Qiao, Ming-Hua [1 ]
Shen, Wei
Xu, Hua-Long [1 ]
Fan, Kang-Nian
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
关键词
Cu/SBA-15; Preparation method; DMM; BDO; Hydrogenolysis; SUPPORTED COPPER-CATALYSTS; CU/SIO2; CATALYSTS; SELECTIVE HYDROGENATION; GAMMA-BUTYROLACTONE; MESOPOROUS SILICA; MALEIC-ANHYDRIDE; SURFACE-AREA; CO OXIDATION; ION-EXCHANGE; TETRAHYDROFURAN;
D O I
10.1016/j.apcata.2008.12.029
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
Mesoporous siliceous SBA-15-supported Cu catalysts have been prepared by different methods and systematically characterized. The results revealed that the incipient wetness impregnation (IWI) method gives poor dispersion of copper species, whereas much better dispersion is found in catalysts prepared by the deposition precipitation (DP), grafting, and homogeneous deposition precipitation (HDP) methods. The Cu/SBA-15 catalyst prepared by the grafting method is rich in Cu+, while a partial destruction of the hexagonal mesostructure of SBA-15 occurs in the catalyst prepared by the HDP method. In gas phase hydrogenolysis of dimethyl maleate (DMM) to 1,4-butanediol (BDO), the hydrogenolysis activities of the catalysts follow the sequence of the metallic Cu surface areas; the catalyst prepared by the HDP method exhibits the highest activity and selectivity. Irrespective of the much smaller metallic Cu surface area of the catalyst prepared by the grafting method, this catalyst exhibits only slightly lower activity than that prepared by the DP method, suggesting that Cu+ also participates in DMM hydrogenolysis. The reaction conditions are further investigated over the Cu/SBA-15 catalyst prepared by the HDP method, aiming to obtain a high yield of BDO. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 136
页数:8
相关论文
共 39 条
[1]  
BARTOK M., 1997, CHEM DOUBLE BONDE SA
[2]  
Brieler FJ, 2002, CHEM-EUR J, V8, P185, DOI 10.1002/1521-3765(20020104)8:1<185::AID-CHEM185>3.0.CO
[3]  
2-L
[4]   ON THE MECHANISM OF NORMAL-BUTANE OXIDATION TO MALEIC-ANHYDRIDE - OXIDATION IN OXYGEN-STOICHIOMETRY-CONTROLLED CONDITIONS [J].
CENTI, G ;
FORNASARI, G ;
TRIFIRO, F .
JOURNAL OF CATALYSIS, 1984, 89 (01) :44-51
[5]   CU/SiO2 catalysts prepared by the ammonia-evaporation method:: Texture, structure, and catalytic performance in hydrogenation of dimethyl oxalate to ethylene glycol [J].
Chen, Liang-Feng ;
Guo, Ping-Jun ;
Qiao, Ming-Hua ;
Yan, Shi-Run ;
Li, He-Xing ;
Shen, Wei ;
Xu, Hua-Long ;
Fan, Kang-Nian .
JOURNAL OF CATALYSIS, 2008, 257 (01) :172-180
[6]   Mesoporous silica-supported Ni-B amorphous alloy catalysts for selective hydrogenation of 2-ethylanthraquinone [J].
Chen, XY ;
Wang, S ;
Zhuang, JH ;
Qiao, MH ;
Fan, KN ;
He, HY .
JOURNAL OF CATALYSIS, 2004, 227 (02) :419-427
[7]   Selective hydrogenation of 2-ethylanthraquinone over an environmentally benign Ni-B/SBA-15 catalyst prepared by a novel reductant-impregnation method [J].
Chen, XY ;
Hu, HR ;
Liu, B ;
Qiao, MH ;
Fan, KN ;
He, HY .
JOURNAL OF CATALYSIS, 2003, 220 (01) :254-257
[8]   NICKEL(II) ION SUPPORT INTERACTIONS AS A FUNCTION OF PREPARATION METHOD OF SILICA-SUPPORTED NICKEL MATERIALS [J].
CLAUSE, O ;
KERMAREC, M ;
BONNEVIOT, L ;
VILLAIN, F ;
CHE, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (12) :4709-4717
[9]   ON THE DETERMINATION OF COPPER SURFACE-AREA BY REACTION WITH NITROUS-OXIDE [J].
EVANS, JW ;
WAINWRIGHT, MS ;
BRIDGEWATER, AJ ;
YOUNG, DJ .
APPLIED CATALYSIS, 1983, 7 (01) :75-83
[10]   True microporosity and surface area of mesoporous SBA-15 silicas as a function of synthesis temperature [J].
Galarneau, A ;
Cambon, H ;
Di Renzo, F ;
Fajula, F .
LANGMUIR, 2001, 17 (26) :8328-8335