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Catalytic CH4 pyrolysis promoted by the interface of a molten metal–salt hybrid system
  • Seo, Jeong Cheol ;
  • Park, Sunju ;
  • Park, Gyeongah ;
  • Lee, Yunjo ;
  • Han, Seung Ju ;
  • Kim, Seok Ki
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Publication Year
2023-07-01
Publisher
Elsevier B.V.
Citation
Gas Science and Engineering, Vol.115
Keyword
Carbon recoveryHydrogen productionMetal-salt interfaceMethane pyrolysisMolten metalMolten salt
Mesh Keyword
Carbon recoveryCatalytic pyrolysisCH 4Chemical energyChemical feedstocksMetal saltMetal-salt interfaceMethane pyrolysisMolten saltReaction beds
All Science Classification Codes (ASJC)
Geotechnical Engineering and Engineering GeologyEnergy Engineering and Power TechnologyFuel TechnologyChemical Engineering (all)
Abstract
Hydrogen is an important chemical feedstock and energy carrier. A promising idea for a bridging technology for net-zero carbon emission is the catalytic pyrolysis of natural gas into hydrogen and solid carbon. However, the activation of methane and recovery of the produced carbon with high purity are the main hurdles for process commercialization. In the present study, molten metal–salt layered reaction beds for methane pyrolysis were investigated to determine the effect of the interface and the optimal ratio of metal and salt. These layered catalyst beds had several advantages over pure molten metal or molten salt catalyst beds. First, the length of the molten metal layer could be minimized to a level where the methane bubbles only touch the metal–salt interface, enhancing the economic feasibility of the process. Second, the metal–salt interface could delay bubble rising in proportion to the interfacial tension. Third, the molten salt layer could wash out the residual metal traces from the produced carbon, improving the carbon purity. This study would provide hints for building economically viable catalytic pyrolysis of methane based on molten metal-salt layered reaction bed.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/33658
DOI
https://doi.org/10.1016/j.jgsce.2023.205017
Fulltext

Type
Article
Funding
This study was financially supported by the KRICT Project ( SI2211-30 ) of the Korea Research Institute of Chemical Technology and Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology ( NRF-2021M3D3A1A01079484 ).
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