Experimental and theoretical analysis revealing the underlying chemistry accounting for the heterogeneous transesterification reaction in Na2SiO3 and Li2SiO3 catalysts

The influence of sodium and lithium content in the metasilicate crystal structure (SiO32-) is herein analyzed concerning the heterogeneous transesterification reaction for biodiesel production. Na2SiO3 and Li2SiO3 were characterized structurally and microstructurally. The catalyst content was evaluated between 1 and 5 wt %, where the maximum conversions to FAME (similar to 99%) were obtained using 3 wt % of Na2SiO3 during 1 h at 65 degrees C. After some cyclic experiments, it was determined that Na2SiO3 possesses a better stability and consequently reutilization capacity than Li2SiO3 in terms of its triglycerides conversion to FAME. DFT calculations were then used to analyze these experimental differences, revealing significant differences between these two catalysts in terms of energy, geometrical configuration, and electronic structure. It was found that three active sites are required on both catalytic surfaces to overcome the methanol deprotonation, which is herein suggested as the rate-controlling step of the entire transesterification mechanism. In one site, the oxygen atom of methanol approaches, while Lewis acid and Bronsted base sites are needed for the methoxide anion stabilization and proton stabilization, respectively. (c) 2021 Elsevier Ltd. All rights reserved.

Automated summary

This study analyzes the influence of sodium and lithium content in the metasilicate crystal structure on the heterogeneous transesterification reaction for biodiesel production. The results show that sodium metasilicate possesses better stability and reutilization capacity compared to lithium metasilicate. DFT calculations reveal significant differences between these two catalysts.