GIEC OpenIR
Experimental study on hydrate-based gas separation of mixed CH4/CO2 using unstable ice in a silica gel bed
Liu, Jun1,2,3,4,5; Ding, Jia-Xiang1,2,3,4,5; Liang, De-Qing1,2,3,4
2018-08-15
Source PublicationENERGY
ISSN0360-5442
Volume157Pages:54-64
Corresponding AuthorLiang, De-Qing(liangdq@ms.giec.ac.cn)
AbstractThe reduction of energy consumed in the hydrate formation process has attracted a great attention in many fields, such as renewable energy resources and environmental issues. In this work, the water and the ice were investigated by powder X-ray diffraction (PXRD) and cryo-scanning electron microscope (SEM) in the silica gel, and the hydrate-based gas separation of CH4/CO2 mixtures was studied at four different pressures (2.6, 3.7, 4.6 and 5.2 MPa) and three different temperatures (271.1, 268.1 and 263.1 K) in silica gel bed. The results showed that water was transformed into discontinuous unstable hexagonal ice crystals on silica gel surface, which was in favor of hydrate formation. Water conversion to hydrate and normalized gas consumption were up to 100% and 0.151 (mol/mol) at 263.1 K and above 4.2 MPa, respectively. CO2 proportion in hydrate, split fraction of CH4 in equilibrium gas and separation factor were up to 99.60%, 99.8% and 257.34 at 2.6 MPa and in the temperature range of 268.1-271.1 K, respectively. It will be of practical interest in relation to losing methane of multistage hydrate-based biogas purification technology. (C) 2018 Elsevier Ltd. All rights reserved.
KeywordBiogas Silica gel Hydrate-based Separation Unstable ice
DOI10.1016/j.energy.2018.05.124
WOS KeywordPRE-COMBUSTION CAPTURE ; SIMULATED LANDFILL GAS ; CARBON-DIOXIDE ; CLATHRATE-HYDRATE ; CO2 CAPTURE ; FLUE-GAS ; PORE STRUCTURE ; NATURAL-GAS ; PHASE-EQUILIBRIA ; CH4 RECOVERY
Indexed BySCI
Language英语
Funding ProjectNational Natural Science Foundation of China[41374149] ; CNPC[2015A-4813] ; CAS[2015A-4813]
WOS Research AreaThermodynamics ; Energy & Fuels
Funding OrganizationNational Natural Science Foundation of China ; CNPC ; CAS
WOS SubjectThermodynamics ; Energy & Fuels
WOS IDWOS:000440876600006
PublisherPERGAMON-ELSEVIER SCIENCE LTD
Citation statistics
Cited Times:52[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.giec.ac.cn/handle/344007/23785
Collection中国科学院广州能源研究所
Corresponding AuthorLiang, De-Qing
Affiliation1.Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Guangdong, Peoples R China
2.CAS Key Lab Gas Hydrate, Guangzhou 510640, Guangdong, Peoples R China
3.Guangdong Prov Key Lab New & Renewable Energy Res, Guangzhou 510640, Guangdong, Peoples R China
4.Chinese Acad Sci, Guangzhou Ctr Gas Hydrate Res, Guangzhou 510640, Guangdong, Peoples R China
5.Univ Chinese Acad Sci, Guangzhou 510640, Guangdong, Peoples R China
First Author AffilicationGuangZhou Institute of Energy Conversion,Chinese Academy of Sciences
Recommended Citation
GB/T 7714
Liu, Jun,Ding, Jia-Xiang,Liang, De-Qing. Experimental study on hydrate-based gas separation of mixed CH4/CO2 using unstable ice in a silica gel bed[J]. ENERGY,2018,157:54-64.
APA Liu, Jun,Ding, Jia-Xiang,&Liang, De-Qing.(2018).Experimental study on hydrate-based gas separation of mixed CH4/CO2 using unstable ice in a silica gel bed.ENERGY,157,54-64.
MLA Liu, Jun,et al."Experimental study on hydrate-based gas separation of mixed CH4/CO2 using unstable ice in a silica gel bed".ENERGY 157(2018):54-64.
Files in This Item:
There are no files associated with this item.
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Liu, Jun]'s Articles
[Ding, Jia-Xiang]'s Articles
[Liang, De-Qing]'s Articles
Baidu academic
Similar articles in Baidu academic
[Liu, Jun]'s Articles
[Ding, Jia-Xiang]'s Articles
[Liang, De-Qing]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Liu, Jun]'s Articles
[Ding, Jia-Xiang]'s Articles
[Liang, De-Qing]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.