Zirconium doped mesoporous silica catalysts for dehydration of glycerol to high added-value products

被引:58
作者
Garcia-Sancho, C. [1 ]
Moreno-Tost, R. [1 ]
Merida-Robles, J. [1 ]
Santamaria-Gonzalez, J. [1 ]
Jimenez-Lopez, A. [1 ]
Maireles-Torres, P. [1 ]
机构
[1] Univ Malaga, Fac Ciencias, Unidad Asociada ICP CSIC, Dept Quim Inorgan Cristalog & Mineral, E-29071 Malaga, Spain
关键词
Mesoporous silica; Glycerol; Zirconium oxide; Acid catalysis; Acrolein; GAS-PHASE DEHYDRATION; SUSTAINABLE PRODUCTION; SELECTIVE OXIDATION; SURFACE-ACIDITY; METAL-OXIDE; ACROLEIN; CONVERSION; ZEOLITE; RATIO;
D O I
10.1016/j.apcata.2012.05.015
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 series of zirconium doped mesoporous silica, with different Si/Zr molar ratios, has been synthesized and tested in the gas-phase dehydration of glycerol. The surface characterization of these solids by using NH3-TPD and pyridine adsorption coupled to FTIR spectroscopy has revealed the existence of well dispersed acid sites, mainly of Lewis type, associated to Zr(IV) species deficiently coordinated located on the pore walls of the siliceous framework. These acid catalysts are active in the glycerol dehydration, increasing the conversion with the zirconium content until values higher than 90 mol% for a Si/Zr molar ratio of 4, at 325 C after 5 h of reaction. However, the catalysts suffer deactivation, which is more important when zirconium oxide is incorporated by impregnation of mesoporous MCM-41 silica. The main reaction products were acrolein, acetaldehyde and acetol. Moreover, the catalysts with a SiZr molar ratio higher than 5 are more selective to acetaldehyde. The acrolein yield was, in all cases, lower than 15 mol% after 24 h of TOS, but a pretreatment under a helium flow saturated with water vapour allows reaching an acrolein yield of 28 mol% and ameliorates the stability of catalysts. The selectivity towards acrolein and hydroxyacetone can be explained by considering the influence of the nature of active sites. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:179 / 187
页数:9
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