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Synthesis of Glycerol Carbonate from Glycerol and Dimethyl Carbonate Catalyzed by Solid Base Catalyst Derived from Waste Carbide Slag

Na2CO3 was loaded onto waste carbide slag (CS) by impregnation-calcination method to prepare the solid base catalyst, which was used to synthesize glycerol carbonate (GC) by the transesterification of glycerol with dimethyl carbonate (DMC). The prepared catalysts were characterized by a scanning ele...

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Bibliographic Details
Published in:International journal of polymer science 2021-12, Vol.2021, p.1-14
Main Authors: Wang, Jianye, Wang, Zhu, Liu, Haifeng, Wang, Song, Sun, Yifeng
Format: Article
Language:English
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Summary:Na2CO3 was loaded onto waste carbide slag (CS) by impregnation-calcination method to prepare the solid base catalyst, which was used to synthesize glycerol carbonate (GC) by the transesterification of glycerol with dimethyl carbonate (DMC). The prepared catalysts were characterized by a scanning electron microscope (SEM), thermogravimetric analysis (TGA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and Brunner−Emmet−Teller (BET) techniques. The catalyst 15 wt.% Na2CO3-CS-800, which was prepared by impregnating CS to the Na2CO3 solution with the concentration of 15 wt.% weight of CS and calcined at 800°C for 3 hours, showed an excellent catalytic ability. When it was applied in the catalytic synthesis of GC, 98.1% glycerol conversion and 96.0% GC yield were achieved in 90 mins at 75°C with the catalyst dosage of 3 wt.% to total reactants and the DMC to glycerol molar ratio of 5. More importantly, the loading of Na2CO3 can effectively improve the reusability of catalyst. The 15 wt.% Na2CO3-CS-800 can still achieve 83.6% glycerol conversion and 80.5% GC yield after five-time reuse. Meanwhile, under the same reaction conditions, the CS-800, which was obtained by calcining CS at 800°C for 3 hours, experienced significant activity reduction with only 15.2% glycerol conversion and 14.1% GC yield after five-time reuse. FTIR and XRD characterization revealed that CO32- might play a key role in preserving active catalytic CaO component by forming protective CaCO3 shell on the catalyst surface.
ISSN:1687-9422
1687-9430
DOI:10.1155/2021/9300442