CAS OpenIR
Promotion of CO2 methanation at low temperature over hydrotalcite-derived catalysts-effect of the tunable metal species and basicity
Guo, Xinpeng1,2; Gao, Denglei2; He, Hongyan2; Traitangwong, Atsadang2; Gong, Maoming2; Meeyoo, Vissanu2; Peng, Zhijian1; Li, Chunshan2,3,4
2021
Source PublicationINTERNATIONAL JOURNAL OF HYDROGEN ENERGY
ISSN0360-3199
Volume46Issue:1Pages:518-530
AbstractThe CO2 methanation is an effective strategy for making full use of waste gases and converting them into valuable chemicals. Nowadays, the key challenge is the design of efficient catalysts to enhance low-temperature catalytic performance. A series of hydrotalcite-derived catalysts with tunable metal species were prepared by hydrothermal synthesis method for CO2 methanation at low-temperature. It was found that suitable synergistic effect between metallic Ni and basic sites in the support could be achieved by regulating the metal composition of hydrotalcite-derived catalysts. The NiMgAl catalyst exhibited the highest catalytic activity with CO2 conversion of 91.8% at 250 degrees C. The in situ DRIFTS measurements and DFT calculation further revealed that the alkaline metal oxide MgO and more Ni(111) active sites in the NiMgAl catalyst could promote the activation of CO2 and the formation of active intermediates, which actively participated in improving lowtemperature activity. Therefore, the ternary mixed oxides catalyst derived from LDHs precursors shows a potential strategy in achieving excellent catalytic properties for CO2 methanation at low-temperature. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
KeywordCO2 methanation Hydrotalcite-derived catalysts Low temperature
DOI10.1016/j.ijhydene.2020.09.193
Language英语
WOS KeywordCARBON-DIOXIDE METHANATION ; DOUBLE HYDROXIDES ; COKE-RESISTANCE ; PARTICLE-SIZE ; HYDROGENATION ; GAS ; CEO2 ; DIBENZOTHIOPHENE ; NANOPARTICLES ; CO-MO/AL2O3
Funding ProjectScience Fund for Creative Research Groups of the National Natural Science Foundation of China[21921005] ; NSFC-NRCT joint project[51661145012] ; National Natural Science Foundation/China[21706258] ; Key Research Program of Frontier Sciences, CAS[QYZDB-SSW-SLH022] ; K. C. Wong Education Foundation[GJTD-2018-04]
WOS Research AreaChemistry ; Electrochemistry ; Energy & Fuels
WOS SubjectChemistry, Physical ; Electrochemistry ; Energy & Fuels
Funding OrganizationScience Fund for Creative Research Groups of the National Natural Science Foundation of China ; NSFC-NRCT joint project ; National Natural Science Foundation/China ; Key Research Program of Frontier Sciences, CAS ; K. C. Wong Education Foundation
WOS IDWOS:000605110100042
PublisherPERGAMON-ELSEVIER SCIENCE LTD
Citation statistics
Document Type期刊论文
Identifierhttp://ir.ipe.ac.cn/handle/122111/43313
Collection中国科学院过程工程研究所
Corresponding AuthorPeng, Zhijian; Li, Chunshan
Affiliation1.China Univ Geosci, Sch Sci, Beijing 100083, Peoples R China
2.Chinese Acad Sci, CAS Key Lab Green Proc & Engn, Natl Key Lab Clean & Efficient Coking Technol,Ins, State Key Lab Multiphase Complex Syst,Beijing Key, Beijing 100190, Peoples R China
3.Zhongke Langfang Inst Proc Engn, Langfang, Hebei, Peoples R China
4.Chinese Acad Sci, Innovat Acad Green Manufacture, Beijing 100190, Peoples R China
Recommended Citation
GB/T 7714
Guo, Xinpeng,Gao, Denglei,He, Hongyan,et al. Promotion of CO2 methanation at low temperature over hydrotalcite-derived catalysts-effect of the tunable metal species and basicity[J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,2021,46(1):518-530.
APA Guo, Xinpeng.,Gao, Denglei.,He, Hongyan.,Traitangwong, Atsadang.,Gong, Maoming.,...&Li, Chunshan.(2021).Promotion of CO2 methanation at low temperature over hydrotalcite-derived catalysts-effect of the tunable metal species and basicity.INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,46(1),518-530.
MLA Guo, Xinpeng,et al."Promotion of CO2 methanation at low temperature over hydrotalcite-derived catalysts-effect of the tunable metal species and basicity".INTERNATIONAL JOURNAL OF HYDROGEN ENERGY 46.1(2021):518-530.
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