Abstract

This study reports the application of metallo-stannosilicates as potential inorganic solid matrixes for enzymes immobilization and their use as a heterogenous catalysts in enzymatic transesterification reactions for the conversion of triacylglycerides into fatty acid ethyl esters (FAEEs). Several stannosilicates were synthesized and physicochemical characterized by X-ray powder diffraction (XRD), scanning electron microscopy with energy dispersive X-ray spectrometry (SEM-EDS), Brunauer-Emmett-Teller (BET)-N2 surface area analysis and solid-state magic-angle spinning nuclear magnetic resonance (MAS NMR 29Si and 119Sn nuclei) techniques. The experimental results for enzymes immobilization were promising, especially for a nickel ion-exchanged metallo-stannosilicate, which were able to immobilize 82 +- 6% of Thermomyces lanuginosus lipase and also kept a high enzymatic activity (42 +- 3 U mg�1). Systematic catalytic reactions for conversion of refined palm oil (Elaeis guineensis) using some of these stannosilicates enzymes complexes yielded 63.3 +- 0.7% of FAEEs. It is worth noticing that, when the transesterification reaction was performed with (a) the as-made stannosilicate without enzymes and (b) the equivalent amount of immobilized Thermomyces lanuginosus lipase in its free form, the FAEEs yield sharply decreased to less than 5.0% and 6.3 +- 0.3%, respectively. This result is a clear evidence of a synergistic effect among the metallo-stannosilicates and the immobilized enzymes.

Highlights

  • The development of alternative biofuels as viable ways to replace or reduce the use of fossil fuels has stimulated the efforts of the scientific community

  • This study reports the application of metallo-stannosilicates as potential inorganic solid matrixes for enzymes immobilization and their use as a heterogenous catalysts in enzymatic transesterification reactions for the conversion of triacylglycerides into fatty acid ethyl esters (FAEEs)

  • Several metallo-stannosilicates were synthesized and characterized by X-ray powder diffraction (XRD), Scanning electron microscopy (SEM), BET-N2 surface area and solid-state MAS NMR (29Si and 119Sn nuclei) techniques. These materials were studied as potential inorganic solid matrixes for immobilization of Thermomyces lanuginosus lipase and as heterogeneous catalysts in the transesterification of refined palm oil (Elaeis guineensis) by ethanolysis reactions

Read more

Summary

Introduction

The development of alternative biofuels as viable ways to replace or reduce the use of fossil fuels has stimulated the efforts of the scientific community. Biodiesel consists of a mixture of fatty acid alkyl esters (FAAEs) and is predominantly produced, in industrial scale, by means of transesterification reactions using refined vegetable oils as triacylglycerides sources, together with short chain alcohols (methanol or ethanol) and homogeneous catalysts. Palm oil is more saturated and has greater oxidation stability when compared to other vegetable oils, in addition to being an important alternative for the sustainable development of some Brazilian regions, mainly in the Amazon[4,5] Another important component in the biodiesel production process is the short chain alcohol source. To the best our knowledge, metallo-stannosilicates were not previously explored as inorganic supports for enzymes immobilization and as heterogeneous catalysts in enzymatic transesterification reactions for biodiesel production by applying the feedstocks (refined palm oil and ethanol) used in this work

Materials
Hydrothermal syntheses of stannosilicates
Nickel ion-exchange experiments
Physicochemical characterization of the solid materials
Solid-state MAS NMR
Zeta potential of the stannosilicates and stannosilicates-lipases complexes
Enzymes immobilization on the stannosilicates
Determination of percentual of enzymes immobilized on the stannosilicates
Enzymatic hydrolytic activity of stannosilicates-enzymes complexes
Physicochemical characterization of the stannosilicates
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call