Structure-reactivity correlations in MgAl hydrotalcite catalysts for biodiesel synthesis

被引:540
作者
Cantrell, DG
Gillie, LJ
Lee, AF
Wilson, K [1 ]
机构
[1] York Univ, Dept Chem, York YO10 5DD, N Yorkshire, England
[2] Univ Sheffield, Dept Engn Mat, Sheffield S1 3JD, S Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
green chemistry; biodiesel; renewable fuel; solid base; hydrotalcite; heterogeneous catalysis; transesterification;
D O I
10.1016/j.apcata.2005.03.027
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 [Mg(1-x)Alx(OH)(2)](x+)(CO3)(x/n)(2-) hydrotalcite materials with compositions over the range x = 0.25-0.55 have been synthesised using an alkali-free coprecipitation route. All materials exhibit XRD patterns characteristic of the hydrotalcite phase with a steady lattice expansion observed with increasing Mg content. XPS measurements reveal a decrease in both the Al and Mg photoelectron binding energies with Mg incorporation which correlates with the increased intra-layer electron density. All materials are effective catalysts for the liquid phase transesterification of glyceryl tributyrate with methanol for biodiesel production. The rate increases steadily with Mg content, with the Mg rich Mg(2.93)AI catalyst an order of magnitude more active than MgO, with pure Al2O3 being completely inert. The rate of reaction also correlates with intralayer electron density which can be associated with increased basicity. (c) 2005 Elsevier B.V. All rights reserved.
引用
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页码:183 / 190
页数:8
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