摘要
Glycerol carbonate (GLC) offers a range of benefits including biodegradability , versatility, and its potential for carbon capture and utilization. Base catalysts play a crucial role for GLC synthesis by facilitating the activation of reactants, enhancing nucleophilicity , accelerating reaction kinetics, and enabling catalyst regeneration . In this study, metal–organic framework (MOF) derived hybrid structure, CaO-MgO@Al 2 O 3 , was developed as a base catalyst to promote transesterification of glycerol with dimethyl carbonate (DMC) to form GLC. The results show that hydrothermal plus wet-impregnation routes formed the hybrid nanostructure with homogenously dispersed Ca, Mg and Al elements. Further, the synthesized catalysts showed significantly high specific surface area and basicity (2.656 mmol g −1 ). High selectivity (>99 %) and high GLC yield (96.2 %; 208.9 mmol g-cat −1 ) were achievable. This study demonstrated the rational design concept of MOF-derived hybrid structures used in the enhancement of base catalysis for transesterification of DMC to GLC, offering an effective solution with mild reaction conditions and high conversion.
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