详细信息

Catalytic transformation of glycerol to 1-propanol by combining zirconium phosphate and supported Ru catalysts  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Catalytic transformation of glycerol to 1-propanol by combining zirconium phosphate and supported Ru catalysts

作者:Wang, Mengpan[1];Yang, Hanmin[2];Xie, Yinzheng[1];Wu, Xiaohui[1];Chen, Chen[1];Ma, Wenbo[1];Dong, Qifeng[1];Hou, Zhenshan[1,3]

机构:[1]E China Univ Sci & Technol, Res Inst Ind Catalysis, Key Lab Adv Mat, Shanghai 200237, Peoples R China;[2]South Cent Univ Nationalities, Key Lab Catalysis & Mat Sci, State Ethn Affairs Commiss, Minist Educ, Wuhan 430074, Hubei Province, Peoples R China;[3]Xinjiang Inst Engn, Dept Chem & Environm Engn, Urumqi 830011, Peoples R China

年份:2016

卷号:6

期号:35

起止页码:29769

外文期刊名:RSC ADVANCES

收录:;EI(收录号:20182205258437);WOS:【SCI-EXPANDED(收录号:WOS:000373029500089)】;

基金:The authors are grateful for support from the National Natural Science Foundation of China (21373082), innovation Program of Shanghai Municipal Education Commission (15ZZ031) and the Fundamental Research Funds for the Central Universities.

语种:英文

外文关键词:Herbicides - Catalyst supports - Aldehydes - Hydrogenolysis - Phosphates - Carbon dioxide - Catalyst selectivity - Chemical reactors - Hydrolysis - Zirconium compounds - Degradation

摘要:The one-pot hydrogenolysis of biomass-derived glycerol to 1-propanol has been investigated over sequential two-layer catalysts in a continuous-flow fixed-bed reactor. The zirconium phosphate layer was packed in the upper layer for dehydration of glycerol into acrolein and the supported Ru catalysts were in the second layer for the sequential hydrogenation of acrolein to 1-propanol. It was observed that the second layer catalyst with the strong acid sites would cause the formation of glycerol degradation products such as methanol, ethanol, methane and carbon dioxide etc., while 2% Ru/SiO2 with weak acid sites afforded the highest selectivity for 1-propanol. The sequential packing of zirconium phosphate and the 2% Ru/SiO2 catalytic system can give full glycerol conversions at 77% selectivity of 1-propanol, as well as exhibiting long-term stability (80 h). Carbonaceous deposits were a main reason for deactivation and the deactivated catalysts can be regenerated conveniently by calcinations in air. The present approach afforded an effective one-pot hydrogenolysis of glycerol to biopropanol, which could bring about the benign development of the biodiesel industry.

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