Synthesis of glycerol carbonate by transesterification of glycerol and dimethyl carbonate over KF/γ-Al2O3 catalyst

• Autor(a) principal: Liu,Zhenmin
• Data de Publicação: 2014
• Outros Autores: Wang,Junwei, Kang,Maoqing, Yin,Ning, Wang,Xinkui, Tan,Yisheng, Zhu,Yulei
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Journal of the Brazilian Chemical Society (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000100019
• topic: glycerol; dimethyl carbonate; glycerol carbonate; KF/γ-A1(2)O3

A series of KF/γ-Al2O3 solid base catalysts were prepared by a wet impregnation method and applied to the synthesis of glycerol carbonate (GC) from glycerol and dimethyl carbonate. The influences of KF loading and calcination temperature of catalyst on the synthesis were investigated. The results showed that KF/γ-Al2O3 catalysts could promote glycerol conversion to GC efficiently. The structure and properties of the catalysts were studied by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), N2-adsorption, CO2-temperature programmed desorption (TPD), X-ray photoelectron spectroscopy (XPS) and Hammett indicator method. It was found that several types of basic centers such as KF, KAlO2, KOH and possibly coordinately unsaturated F- ion existed on the catalysts. The strong basic centers could not only accelerate the conversion of glycerol, but also enhance the formation of glycidol from the decomposition of GC. The recycling of KF/γ-Al2O3 revealed that deactivation of catalyst was strengthened with the reuse times, which was mainly caused by the partial leaching of active potassium species. High calcination temperature favored the transformation of KF to KAlO2 and alleviated the deactivation of the catalyst. Based on the product distribution and obtained results, a possible reaction mechanism on reaction of glycerol with dimethyl carbonate was proposed.