中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
chemoselectivehydrogenolysisoftetrahydrofurfurylalcoholto15pentanedioloverirmooxsio2catalyst

文献类型:期刊论文

作者Wang Zhiqiang2; Pholjaroen Boonrat2; Li Mengxia2; Dong Wenjun1; Li Ning2; Wang Aiqin2; Wang Xiaodong2; Cong Yu2; Zhang Tao2
刊名journalofenergychemistry
出版日期2014-01-01
卷号23期号:4页码:427
ISSN号2095-4956
英文摘要In this work, MoO x promoted Ir 2 catalysts were prepared and used for the selective hydrogenolysis of tetrahydrofurfuryl alcohol (THFA) to 1,5-pentanediol in a continuous flow reactor. The effects of different noble metals (Ir, Pt, Pd, Ru, Rh), supports and Ir contents were screened. Among the investigated catalysts, 4 wt%Ir-MoO x 2 with a Mo x species attached on them is essential for the excellent catalytic performance of Ir-MoO x 2 . The catalyst exhibited a better hydrogenolysis efficiency of THFA with the selectivity of 1,5-pentanediol of 65%–74% at a conversion of THFA of 70%–75% when the initial THFA concentration is ranging from 20 wt% and 40 wt%. And higher system pressure was also in favor of the conversion of THFA. During a stability test, the conversion of THFA and 1,5-pentanediol yield over Ir-MoO x 2 decreased with reaction time, which can be explained by the leaching of Mo species during the reaction.
语种英语
源URL[http://cas-ir.dicp.ac.cn/handle/321008/177146]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.浙江理工大学
2.中国科学院大连化学物理研究所
推荐引用方式
GB/T 7714
Wang Zhiqiang,Pholjaroen Boonrat,Li Mengxia,et al. chemoselectivehydrogenolysisoftetrahydrofurfurylalcoholto15pentanedioloverirmooxsio2catalyst[J]. journalofenergychemistry,2014,23(4):427.
APA Wang Zhiqiang.,Pholjaroen Boonrat.,Li Mengxia.,Dong Wenjun.,Li Ning.,...&Zhang Tao.(2014).chemoselectivehydrogenolysisoftetrahydrofurfurylalcoholto15pentanedioloverirmooxsio2catalyst.journalofenergychemistry,23(4),427.
MLA Wang Zhiqiang,et al."chemoselectivehydrogenolysisoftetrahydrofurfurylalcoholto15pentanedioloverirmooxsio2catalyst".journalofenergychemistry 23.4(2014):427.

入库方式: OAI收割

来源:大连化学物理研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。