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

• Three Keggin HPA are immobilized on the silica through the link of zirconia.
• PW–ZrO2/SiO2 and SiW–ZrO2/SiO2 form stronger bonds with the support than PMo–ZrO2/SiO2 which contributes to the leaching.
• Stronger interaction HPA-support is due to the lower polarizability of the bonds Zr–O–W compared to the Zr–O–Mo.
• PW–ZrO2/SiO2 and SiW–ZrO2/SiO2 do not leach in oleic acid medium showing their potential toward industrial applications.

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 H3PMo12O40, 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.

Figure optionsDownload high-quality image (49 K)Download as PowerPoint slide