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Direct Hydrogenolysis of Cellulose into Methane under Mild Conditions
Wang, Haiyong1,2,3,4; Zhang, Caihong1,2,3,4; Liu, Qiying1,2,3; Zhu, Changhui1,2,3,4; Chen, Lungang1,2,3; Wang, Chenguang1,2,3; Ma, Longlong1,2,3
2018-11-01
Source PublicationENERGY & FUELS
ISSN0887-0624
Volume32Issue:11Pages:11529-11537
Corresponding AuthorWang, Haiyong() ; Zhang, Caihong() ; Liu, Qiying(liuqy@ms.giec.ac.cn)
AbstractCH4 is a clean fuel due to the highest H/C atom ratio among the other hydrocarbon fuels, showing less carbon emission during combustion. The traditional CH4 production by fermentation presents the obvious disadvantages of low CH4 yield (50-75%) and high CO2 emission (25-50%). Herein, an efficient direct conversion of cellulose to CH4 was investigated by using several hydrogenation catalysts. The Ru/C catalyst showed the excellent catalytic performance among all the studied catalysts. The optimized reaction parameters including temperature, time, pressure, and catalyst dosage were further investigated by using Ru/C catalyst, and the maximum CH4 yield of 88.1% was obtained at mild reaction conditions (220 degrees C and 1 MPa initial H-2). This value obtained is the highest yield for the production of CH4 from cellulose to date. The reaction network suggests that the hydrolysis, hydrogenation, decarbonylation, retro-aldol reaction, and aqueous-phase-reforming are probably taking place, in which cellulose hydrolysis was proven to be the rate-determined step. This work provided an efficient approach to produce biomass derived CH4 with extreme CO2 emission (below 5%) and a better understanding of the cellulose hydrogenolysis process.
DOI10.1021/acs.energyfuels.8b02235
WOS KeywordSUPERCRITICAL WATER ; HYDROTHERMAL CONVERSION ; BIOMETHANE PRODUCTION ; ANAEROBIC-DIGESTION ; C-C ; BIOMASS ; GASIFICATION ; GLYCEROL ; HYDRODEOXYGENATION ; HYDROCARBONS
Indexed BySCI
Language英语
Funding ProjectNational Natural Science Foundation of China[51576199] ; National Natural Science Foundation of China[51536009] ; Natural Science Foundation of Guangdong Province[2017A030308010] ; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program[2017BT01N092]
WOS Research AreaEnergy & Fuels ; Engineering
Funding OrganizationNational Natural Science Foundation of China ; Natural Science Foundation of Guangdong Province ; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program
WOS SubjectEnergy & Fuels ; Engineering, Chemical
WOS IDWOS:000451101300045
PublisherAMER CHEMICAL SOC
Citation statistics
Cited Times:16[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.giec.ac.cn/handle/344007/24279
Collection中国科学院广州能源研究所
Corresponding AuthorWang, Haiyong; Zhang, Caihong; Liu, Qiying
Affiliation1.Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Guangdong, Peoples R China
2.Chinese Acad Sci, Key Lab Renewable Energy, Guangzhou 510640, Guangdong, Peoples R China
3.Guangdong Key Lab New & Renewable Energy Res & De, Guangzhou 510640, Guangdong, Peoples R China
4.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
First Author AffilicationGuangZhou Institute of Energy Conversion,Chinese Academy of Sciences
Recommended Citation
GB/T 7714
Wang, Haiyong,Zhang, Caihong,Liu, Qiying,et al. Direct Hydrogenolysis of Cellulose into Methane under Mild Conditions[J]. ENERGY & FUELS,2018,32(11):11529-11537.
APA Wang, Haiyong.,Zhang, Caihong.,Liu, Qiying.,Zhu, Changhui.,Chen, Lungang.,...&Ma, Longlong.(2018).Direct Hydrogenolysis of Cellulose into Methane under Mild Conditions.ENERGY & FUELS,32(11),11529-11537.
MLA Wang, Haiyong,et al."Direct Hydrogenolysis of Cellulose into Methane under Mild Conditions".ENERGY & FUELS 32.11(2018):11529-11537.
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