DICP OpenIR
Production of hydrogen by aqueous-phase reforming of glycerol
Wen, Guodong1,2; Xu, Yunpeng1; Ma, Huaijun1,2; Xu, Zhusheng1; Tian, Zhijian1,3; Tian ZJ(田志坚)
KeywordHydrogen Aqueous-phase Reforming Glycerol
Source PublicationINTERNATIONAL JOURNAL OF HYDROGEN ENERGY
2008-11-01
DOI10.1016/j.ijhydene.2008.07.072
Volume33Issue:22Pages:6657-6666
Indexed BySCI
SubtypeArticle
Department8
Funding Project802
Contribution Rank1;1
WOS HeadingsScience & Technology ; Physical Sciences ; Technology
WOS SubjectChemistry, Physical ; Electrochemistry ; Energy & Fuels
WOS Research AreaChemistry ; Electrochemistry ; Energy & Fuels
WOS KeywordSUPPORTED METAL-CATALYSTS ; FUEL-CELL ; BIOMASS ; GENERATION ; CONVERSION ; ENERGY ; GASIFICATION ; HYDROCARBONS ; CELLULOSE ; ALCOHOLS
AbstractThe activities and stabilities of Pt, Ni, Co, and Cu catalysts for H(2) production by aqueous-phase reforming of glycerol, as well as the effect of support on activity and stability, were studied using a fixed-bed flow reactor. Both of the fresh and spent catalysts were characterized by XRD, N(2) adsorption/desorption, TPO, H(2)-TPR, and H(2) chemisorption. It was found that the activity of the metal catalysts increased in the order of Co, Ni, Cu. and Pt. Additionally, Pt was highly stable, whereas Ni and Cc showed significant deactivation with time on stream. It was also found that the activity of supported Pt catalysts was given as follows: SAPO-11 < AC(active carbon) < HUSY < SiO(2) < MgO < Al(2)O(3). Moreover, basic support resulted in high activity and higher hydrogen molar concentration, whereas acidic support and neutral Al(2)O(3) support tended to increase alkane formation. It was shown by XRD that Pt was caused to sinter on all of the supported Pt catalysts during the reaction. In addition, trace amount of carbon deposition was found on all of the supported Pt catalysts. However, no remarkable deactivation was observed over Pt/Al(2)O(3), Pt/SiO(2), Pt/AC, and Pt/HUSY catalysts. Noteworthy was the investigation of the two zeolite-supported catalysts. However, low activities as well as the collapse of the support were obtained. In addition, little influence of the collapse of the support on the stability of Pt/HUSY was observed, whereas Pt/SAPO-11 exhibited remarkable deactivation. (C) 2008 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
Language英语
URL查看原文
WOS IDWOS:000261543400029
Citation statistics
Cited Times:210[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://cas-ir.dicp.ac.cn/handle/321008/101449
Collection中国科学院大连化学物理研究所
Corresponding AuthorTian ZJ(田志坚)
Affiliation1.Chinese Acad Sci, Dalian Inst Chem Phys, Lab Appl Catalysis, Dalian 116023, Peoples R China
2.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
3.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
Recommended Citation
GB/T 7714
Wen, Guodong,Xu, Yunpeng,Ma, Huaijun,et al. Production of hydrogen by aqueous-phase reforming of glycerol[J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,2008,33(22):6657-6666.
APA Wen, Guodong,Xu, Yunpeng,Ma, Huaijun,Xu, Zhusheng,Tian, Zhijian,&田志坚.(2008).Production of hydrogen by aqueous-phase reforming of glycerol.INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,33(22),6657-6666.
MLA Wen, Guodong,et al."Production of hydrogen by aqueous-phase reforming of glycerol".INTERNATIONAL JOURNAL OF HYDROGEN ENERGY 33.22(2008):6657-6666.
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