Solvent effect on the preparation of H3PW12O40 supported on alumina

被引:56
作者
Caliman, E [1 ]
Dias, JA [1 ]
Dias, SCL [1 ]
Prado, AGS [1 ]
机构
[1] Univ Brasilia, Inst Quim, Lab Catalise, BR-70904970 Brasilia, DF, Brazil
关键词
12-tungstophosphoric acid; alumina; supported heteropolyacid; acidity; P-31; MAS-NMR;
D O I
10.1016/j.cattod.2005.07.102
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Preparation, structural characterization and solid acidity studies of H3PW12O40 (H3PW) supported (20, 40, 50 and 80 wt.%) on gamma-alumina have been performed. Impregnation of H3PW on gamma-alumina was performed by the evaporation technique using water (acidified with HCI), ethanol and acetonitrile as solvents. The presence of the Keggin anion on alumina surface is very dependent upon the preparation conditions and pH, as indicated by partial decomposition in water solution. High acid concentration in aqueous solutions is required to obtain intact the Keggin anion. Ethanol showed the formation of distinct species on the alumina surface. In contrast, acetonitrile has not displayed any significant decomposition of the Keggin anion. All these, conclusions are based on FTIR, Raman P-31 MAS-NMR, XRD and SEM-EDX measurements. The presence of the Keggin structure on the alumina surface can be followed by those techniques, eliminating any doubt about collapse of the supported anion. Calorimetric and adsorption of pyridine interactions in cyclohexane slurry (Cal-ad method) showed that the catalyst H3PW/Al2O3 is a weaker acid than pure H3PW or supported on silica, but stronger than alumina. The enthalpies indicated partial neutralization of the most basic sites of alumina at the expense of the strongest protons of H3PW. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:816 / 825
页数:10
相关论文
共 37 条
[1]  
[Anonymous], CATALYSIS FINE CHEM
[2]   Supported heteropolyacid (HPW) catalysts for the continuous alkylation of isobutane with 2-butene: The benefit of using MCM-41 with larger pore diameters [J].
Blasco, T ;
Corma, A ;
Martinez, A ;
Martinez-Escolano, P .
JOURNAL OF CATALYSIS, 1998, 177 (02) :306-313
[3]   DETERMINATION OF HYDROGEN-BONDING ACID SITES ON SILICA USING THE CAL-AD METHOD [J].
CHRONISTER, CW ;
DRAGO, RS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (11) :4793-4798
[4]   INORGANIC SOLID ACIDS AND THEIR USE IN ACID-CATALYZED HYDROCARBON REACTIONS [J].
CORMA, A .
CHEMICAL REVIEWS, 1995, 95 (03) :559-614
[5]   Multiple adsorption process description of zeolite mordenite acidity [J].
de Macedo, JL ;
Dias, SCL ;
Dias, JA .
MICROPOROUS AND MESOPOROUS MATERIALS, 2004, 72 (1-3) :119-125
[6]   The solid acidity of 12-tungstophosphoric acid [J].
Dias, JA ;
Osegovic, JP ;
Drago, RS .
JOURNAL OF CATALYSIS, 1999, 183 (01) :83-90
[7]   Effects of cesium ion exchange on acidity of 12-tungstophophoric acid [J].
Dias, JA ;
Caliman, E ;
Dias, SCL .
MICROPOROUS AND MESOPOROUS MATERIALS, 2004, 76 (1-3) :221-232
[8]   Preparation and characterization of supported H3PW12O40 on silica gel:: a potential catalyst for green chemistry processes [J].
Dias, JA ;
Caliman, E ;
Dias, SCL ;
Paulo, M ;
de Souza, ATCP .
CATALYSIS TODAY, 2003, 85 (01) :39-48
[9]   Dehydration of 1-propanol using H3PW12O40 as catalyst [J].
Dias, JA ;
Dias, SCL ;
Kob, NE .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 2001, (03) :228-231
[10]   Acidity measurements of zeolite Y by adsorption of several probes [J].
Dias, SCL ;
de Macedo, JL ;
Dias, JA .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (24) :5574-5579