CO/SiO2 catalysts for selective hydrogenation of crotonaldehyde -: III.: Promoting effect of zinc

被引:34
作者
Rodrigues, EL [1 ]
Bueno, JMC [1 ]
机构
[1] Univ Fed Sao Carlos, Dept Chem Engn, BR-13565905 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
cobalt-zinc catalysts; desorption of hydrogen; desorption of CO; crotonaldehyde hydrogenation; Co-ZnO/SiO2;
D O I
10.1016/j.apcata.2003.07.002
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
ZnO-CO/SiO2 catalysts with various cobalt loadings and Co/Zn ratios were studied in terms of both their surface structure and catalytic hydrogenation of crotonaldehyde (CROALD), to investigate the influence of zinc on the properties Of CO/SiO2 catalysts. The ZnO-CoOx precursors were prepared in situ on the silica support by co-impregnation of the support with an aqueous solution of cobalt and zinc nitrates. The oxide precursors and catalysts were characterized by temperature-programmed reduction (TPR), temperature-programmed desorption of hydrogen (TPD-H-2), and diffuse reflectance FTIR spectroscopy (DRIFTS) of adsorbed CO. The TPD-H-2 and DRIFTS of CO indicated that the presence of Zn suppresses formation of the type alpha sites present in catalysts containing only Co and promotes surface-structure formation of ZnOx-Co sites obtained by reduction of the catalysts at high temperatures. The presence of ZnOx in the surface structure blocks both CO adsorption in bridge form and the formation of the hydrocarbonyl structure in the presence of H-2. For crotonaldehyde hydrogenation in the gas phase, selective hydrogenation of C=C or C=O groups was correlated with the relative proportion of species in the oxide precursors. The formation of ZnOx-Co at the surface strongly suppresses the C=C hydrogenation activity. However, this surface structure is not stable during prolonged catalytic runs. After a time on stream, the catalytic properties revert to those of the unpromoted catalysts. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:201 / 211
页数:11
相关论文
共 46 条
[1]   Selective hydrogenation of aldehyde groups in various α,β-unsaturated aldehydes over alumina-supported cobalt (0) catalyst [J].
Ando, C ;
Kurokawa, H ;
Miura, H .
APPLIED CATALYSIS A-GENERAL, 1999, 185 (02) :L181-L183
[2]   TRANSIENT IR SPECTROSCOPIC INVESTIGATION OF SURFACE-CARBONYL FORMATION ON A SUPPORTED COBALT CATALYST [J].
ANSORGE, J ;
FORSTER, H .
JOURNAL OF CATALYSIS, 1981, 68 (01) :182-185
[3]   Hydrogenation of citral on activated carbon and high-surface-area graphite-supported ruthenium catalysts modified with iron [J].
Bachiller-Baeza, B ;
Guerrero-Ruiz, A ;
Wang, P ;
Rodríguez-Ramos, I .
JOURNAL OF CATALYSIS, 2001, 204 (02) :450-459
[4]   Influence of Mg and Ce addition to ruthenium based catalysts used in the selective hydrogenation of α,β-unsaturated aldehydes [J].
Bachiller-Baeza, B ;
Rodríguez-Ramos, I ;
Guerrero-Ruiz, A .
APPLIED CATALYSIS A-GENERAL, 2001, 205 (1-2) :227-237
[5]   NOVEL CLUSTER-DERIVED CATALYSTS FOR THE SELECTIVE HYDROGENATION OF CROTONALDEHYDE [J].
BANARES, M ;
PATIL, AN ;
FEHLNER, TP ;
WOLF, EE .
CATALYSIS LETTERS, 1995, 34 (3-4) :251-258
[6]   CROTONALDEHYDE AND METHYLCROTONALDEHYDE HYDROGENATION OVER PT(111) AND PT80FE20(111) SINGLE-CRYSTALS [J].
BECCAT, P ;
BERTOLINI, JC ;
GAUTHIER, Y ;
MASSARDIER, J ;
RUIZ, P .
JOURNAL OF CATALYSIS, 1990, 126 (02) :451-456
[7]   SURFACE ORGANOMETALLIC CHEMISTRY ON METALS - A NOVEL AND EFFECTIVE ROUTE TO CUSTOM-DESIGNED BIMETALLIC CATALYSTS [J].
CANDY, JP ;
DIDILLON, B ;
SMITH, EL ;
SHAY, TB ;
BASSET, JM .
JOURNAL OF MOLECULAR CATALYSIS, 1994, 86 (1-3) :179-204
[8]   HYDROGENATION ACTIVITY AND SELECTIVITY OF COBALT BORIDES [J].
CHEN, YZ ;
WU, KJ .
APPLIED CATALYSIS, 1991, 78 (02) :185-197
[9]   EFFECT OF PROMOTER ON SELECTIVE HYDROGENATION OF ALPHA,BETA-UNSATURATED ALDEHYDES OVER COBALT BORIDES [J].
CHEN, YZ ;
WEI, SW ;
WU, KJ .
APPLIED CATALYSIS A-GENERAL, 1993, 99 (02) :85-96
[10]   IR AND TPD STUDY OF FRESH AND CARBON-DEPOSITED CO/AL2O3 CATALYSTS [J].
CHOI, JG ;
RHEE, HK ;
MOON, SH .
APPLIED CATALYSIS, 1985, 13 (02) :269-280