Cu/SiO2 catalysts for methanol to methyl formate dehydrogenation -: A comparative study using different preparation techniques

被引:95
作者
Guerreiro, ED
Gorriz, OF
Larsen, G
Arrúa, LA
机构
[1] UNSL, CONICET, INTEQUI, RA-5700 San Luis, Argentina
[2] Univ Nebraska, Dept Chem Engn, Lincoln, NE 68588 USA
基金
美国国家科学基金会;
关键词
copper/silica; preparation methods; dehydrogenation; methanol; methyl formate;
D O I
10.1016/S0926-860X(00)00507-X
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 comparative study of the different preparation conditions required to produce supported copper catalysts by the wet impregnation (VIII) and the ion-exchange (IE) methods has been carried out. Two silicas with different textural characteristics, and one form of naturally occurring pumice were used as supports. In order to obtain specific chemical species of copper in solution as well as different support reactivities, three different pH values (1, 4.5 and 1 1.5) for the impregnating solution were tested, The catalysts were characterized by means of different techniques, such as XFS, BET, TPR, dissociative chemisorption of N2O, XRD, TEM. EXAFS and XANES and methanol (MeOH) dehydrogenation. The use of copper solutions with high pH, especially after several hours of contact with the chosen carrier, with high solution volume to pore volume ratios, modifies strongly the support texture decreasing the: specific surface areas (SSA) of the final catalyst, Copper particle sizes lower than a critical limit, or that did not fulfill a certain ensemble requirement, were not active for methanol dehydrogenation indicating that below such limit, this might be a structure-sensitive reaction. A catalyst (WI-11A) prepared by a simple incipient wetness impregnation method at an alkaline pH similar to that used for the IE technique, showed high dispersion and it was simply activated under reaction conditions (MeOH/N-2, 230 degreesC) giving conversions around 50% and selectivities to methyl formate (MF) in the order of 75-80% with no deactivation observed after 3 h of time on stream. (C) 2000 Elsevier Science B,V. All rights reserved.
引用
收藏
页码:33 / 48
页数:16
相关论文
共 28 条
[1]   DEHYDROGENATION OF METHANOL TO METHYL FORMATE OVER COPPER-BASED CATALYSTS [J].
AI, M .
APPLIED CATALYSIS, 1984, 11 (2-3) :259-270
[2]  
[Anonymous], 1994, ADV CHEM SERIES, DOI DOI 10.1002/9780470926819
[3]   AN IMPROVED PROCEDURE FOR ESTIMATING THE METAL-SURFACE AREA OF SUPPORTED COPPER-CATALYSTS [J].
BOND, GC ;
NAMIJO, SN .
JOURNAL OF CATALYSIS, 1989, 118 (02) :507-510
[4]  
CHINCHEN GC, 1987, CATAL, V103, P7
[5]  
Cvetanovic R.J., 1967, ADV CATAL, V17, P103, DOI [DOI 10.1016/S0360-0564(08)60686-0, 10.1016/S0360-0564, DOI 10.1016/S0360-0564]
[6]  
DVORAK B, 1970, J CATAL, V18, P108
[7]   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
[8]   A MICROCALORIMETRIC METHOD FOR THE EVALUATION OF COPPER SURFACE-AREA IN CU-ZNO CATALYST [J].
GIAMELLO, E ;
FUBINI, B ;
LAURO, P ;
BOSSI, A .
JOURNAL OF CATALYSIS, 1984, 87 (02) :443-451
[9]   Characterization of Cu/SiO2 catalysts prepared by ion exchange for methanol dehydrogenation [J].
Guerreiro, ED ;
Gorriz, OF ;
Rivarola, JB ;
Arrua, LA .
APPLIED CATALYSIS A-GENERAL, 1997, 165 (1-2) :259-271
[10]   DEHYDROGENATION OF METHANOL TO METHYL FORMATE OVER SUPPORTED COPPER-CATALYSTS [J].
GUERRERORUIZ, A ;
RODRIGUEZRAMOS, I ;
FIERRO, JLG .
APPLIED CATALYSIS, 1991, 72 (01) :119-137