An FT-IR study of the adsorption of isopropanol on calcined layered double hydroxides containing isopolyrnolybdate

被引:21
作者
Carriazo, Daniel [1 ]
Martin, Cristina [1 ]
Rives, Vicente [1 ]
机构
[1] Univ Salamanca, Dept Quim Inorgan, E-37008 Salamanca, Spain
关键词
hydrotalcite; polyoxometalates; dehydrogenation;
D O I
10.1016/j.cattod.2006.10.009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The acid-base and red-ox properties of amorphous magnesium and zinc molybdates obtained through calcination at 400 degrees C of Mg(2)Al- and Zn(2)Al-heptamolybdate layered double hydroxides, which had been prepared by anionic exchange from the corresponding nitrate -hydrotalcite precursors, have been studied. Lewis-type acid and basic sites have been detected in both systems, in addition to Bronsted-type acid sites in magnesium molybdate; however, as studied by FT-IR spectroscopy, none of them is strong enough to yield propene through isopropanol decomposition. The higher reducibility of Mo(6+) cations in zinc-containing samples than the magnesium containing ones makes them more selective for acetone production. Moreover, a small amount of products formed on basic sites through acetone aldol reaction have been identified at high reaction temperatures. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:153 / 161
页数:9
相关论文
共 47 条
[1]   Mo/γ-Al2O3 catalysts for the oxidative dehydrogenation of propane.: Effect of Mo loading [J].
Abello, MC ;
Gomez, MF ;
Ferretti, O .
APPLIED CATALYSIS A-GENERAL, 2001, 207 (1-2) :421-431
[2]   ACETATES AND ACETATO-COMPLEXES .2. SPECTROSCOPIC STUDIES [J].
ALCOCK, NW ;
TRACY, VM ;
WADDINGTON, TC .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1976, (21) :2243-2246
[3]   Oxidative dehydrogenation of propane over calcined vanadate-exchanged Mg,Al-layered double hydroxides [J].
Bahranowski, K ;
Bueno, G ;
Corberán, VC ;
Kooli, F ;
Serwicka, EM ;
Valenzuela, RX ;
Wcislo, K .
APPLIED CATALYSIS A-GENERAL, 1999, 185 (01) :65-73
[4]  
Barriga C, 1997, CHEM INDUST, V69, P661
[5]   Quantitative determination of the number of surface active sites and the turnover frequency for methanol oxidation over bulk metal vanadates [J].
Briand, LE ;
Jehng, JM ;
Cornaglia, L ;
Hirt, AM ;
Wachs, IE .
CATALYSIS TODAY, 2003, 78 (1-4) :257-268
[6]   Quantitative determination of the number of surface active sites and the turnover frequencies for methanol oxidation over metal oxide catalysts: Application to bulk metal molybdates and pure metal oxide catalysts [J].
Briand, LE ;
Hirt, AM ;
Wachs, IE .
JOURNAL OF CATALYSIS, 2001, 202 (02) :268-278
[7]   A FT-IR study of the reactivity of tungsta-supported catalysts toward butan-2-ol [J].
Carrazán, SRG ;
Martín, C ;
Solana, G ;
Rives, V .
LANGMUIR, 2001, 17 (22) :6968-6973
[8]   Structural and texture evolution with temperature of layered double hydroxides intercalated with paramolybdate anions [J].
Carriazo, D ;
Domingo, C ;
Martín, C ;
Rives, V .
INORGANIC CHEMISTRY, 2006, 45 (03) :1243-1251
[9]   HYDROTALCITE-TYPE ANIONIC CLAYS: PREPARATION, PROPERTIES AND APPLICATIONS [J].
Cavani, F. ;
Trifiro, F. ;
Vaccari, A. .
CATALYSIS TODAY, 1991, 11 (02) :173-301
[10]   SELECTIVE OXIDATIVE DEHYDROGENATION OF PROPANE OVER V-MG-O CATALYSTS [J].
CHAAR, MA ;
PATEL, D ;
KUNG, HH .
JOURNAL OF CATALYSIS, 1988, 109 (02) :463-467