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Hydrogenolysis of glycerol over TiO(2)-supported Pt-WO(x) catalysts: Effects of the TiO(2) crystal phase and WO(x) loading

The selective hydrogenolysis of glycerol to 1,3-propanediol (1,3-PDO) with high added value is attraction but challenging. Pt-WO(x)-based catalysts have been extensively studied in the selective hydrogenolysis of glycerol. The catalyst support and the physicochemical state of WO(x) play important ro...

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Detalles Bibliográficos
Autores principales: Wang, Yaju, Zhou, Zhiming, Wang, Chao, Zhao, Leihong, Xia, Qineng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532750/
https://www.ncbi.nlm.nih.gov/pubmed/36212063
http://dx.doi.org/10.3389/fchem.2022.1004925
Descripción
Sumario:The selective hydrogenolysis of glycerol to 1,3-propanediol (1,3-PDO) with high added value is attraction but challenging. Pt-WO(x)-based catalysts have been extensively studied in the selective hydrogenolysis of glycerol. The catalyst support and the physicochemical state of WO(x) play important roles on this reaction. In this paper, Pt-WO(x) catalysts supported on TiO(2) with different crystal forms were prepared and studied for their catalytic performance in hydrogenolysis of glycerol. It was observed that the catalytic performance of anatase-type (A-type) TiO(2)-supported catalyst (Pt/W/A-Ti) is much better than that of the rutile-type (R-type) TiO(2) catalyst (Pt/W/R-Ti) due to its higher stability. Furthermore, the influence of W loading amount and state were thoroughly investigated for the Pt/W/A-Ti catalysts, and Pt/W/A-TiO(2) with 5 wt% loading of WO(x) achieved the best catalytic performance (100% conversion of glycerol and 41% yield of 1,3-PDO under the optimal reaction conditions), owing to the suitable WO(x) domains and high dispersion of W species, as evidenced by XRD patterns and TEM images. Mechanism study by in-situ DRIFTS experiments indicated that glycerol was first converted to 3-hydroxypropanal and then converted to 1,3-PDO through subsequent reactions.