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Immobilizing heteropolyacids on zirconia-modified silica as catalysts for oleochemistry transesterification and esterification reactions

机译:将杂多酸固定在氧化锆改性的二氧化硅上,作为油化学酯交换反应和酯化反应的催化剂

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摘要

A new method of chemical immobilization of Keggin heteropolyacids (HPAs) was suggested. H3PW12O40, H4SiW12O40, and H3PMo12O40 were immobilized on the silica which was previously grafted with zirconium butoxide. The immobilization method promoted strong interaction HPA-support and yielded 25 wt.% of well-dispersed HPAs, so increasing the density of acid sites. The catalysts were active in the reaction of transesterification of methyl stearate with n-butanol and esterification of oleic acid with trimethylolpropane. We demonstrate that, contrary to the immobilized H3PW12O40, the H3PW12O40 and H4SiW12O40-based catalysts are stable toward leaching in a non-polar oleic acid medium. A discussion on circumventing the leaching in non-polar versus polar media is proposed in terms of interaction strength HPA-support. The stronger interaction (i.e., better resistance for leaching) between the support and H3PW12O40 (or H4SiW12O40) is referred to the lower difference of electronegativity between Zr and W and the lower polarizability of the bonds Zr-O-W compared to Zr-O-Mo. (C) 2014 Elsevier Inc. All rights reserved.
机译:提出了一种化学固定Keggin杂多酸(HPA)的新方法。将H3PW12O40,H4SiW12O40和H3PMo12O40固定在事先已接有丁氧化锆的二氧化硅上。固定化方法促进了HPA载体的强相互作用,并产生了25 wt。%的HPA分散均匀,因此增加了酸性位点的密度。所述催化剂在硬脂酸甲酯与正丁醇的酯交换反应和油酸与三羟甲基丙烷的酯化反应中具有活性。我们证明,与固定的H3PW12O40相反,基于H3PW12O40和H4SiW12O40的催化剂在非极性油酸介质中对浸出稳定。根据相互作用强度HPA-support,提出了关于在非极性介质与极性介质中规避浸出的讨论。载体与H3PW12O40(或H4SiW12O40)之间的较强相互作用(即,更好的耐浸出性)是指Zr和W之间的电负性差异较小,且Zr-O-W键的极化率与Zr-O-Mo相比较低。 (C)2014 Elsevier Inc.保留所有权利。

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