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    Hydrogen Production by Carbon-Catalyzed Methane Decomposition Via Thermogravimetry

    Source: Journal of Energy Resources Technology:;2017:;volume( 139 ):;issue: 001::page 12005
    Author:
    Shilapuram, Vidyasagar
    ,
    Ozalp, Nesrin
    DOI: 10.1115/1.4035145
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Hydrogen is a high energy content fuel and methane is currently the most preferred feedstock for hydrogen production. Direct thermal splitting of methane offers the cleanest technique to produce hydrogen and carbon as coproduct fuel. Carbonaceous catalysts have significant impact on methane to hydrogen conversion. This study presents thermogravimetric experiment results of carbon-catalyzed methane decomposition using commercial catalyst. Results are presented in terms of carbon formation rate, amount of carbon deposition on the catalyst, sustainability factor, catalyst activity, and kinetics of the reaction. The results show that weight gain because of carbon formation depends on reaction temperature, methane volume percent in the feed gas, and nature of the carbonaceous catalyst. It was observed that the reaction rate was dominant at the beginning, and deactivation rate was dominant toward the end of reaction. X-ray diffraction (XRD) and scanning electron microscopic (SEM) analysis of deactivated catalytic samples show decreasing disorder with increasing reaction temperature. Finally, performance comparison of activated carbons (ACs) studied in literature shows that activated carbon sample chosen in this study outperforms in terms of carbon deposition, reaction rate, carbon weight gain, and sustainability factor.
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      Hydrogen Production by Carbon-Catalyzed Methane Decomposition Via Thermogravimetry

    URI
    http://yetl.yabesh.ir/yetl1/handle/yetl/4236882
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    contributor authorShilapuram, Vidyasagar
    contributor authorOzalp, Nesrin
    date accessioned2017-11-25T07:21:06Z
    date available2017-11-25T07:21:06Z
    date copyright2016/29/11
    date issued2017
    identifier issn0195-0738
    identifier otherjert_139_01_012005.pdf
    identifier urihttp://138.201.223.254:8080/yetl1/handle/yetl/4236882
    description abstractHydrogen is a high energy content fuel and methane is currently the most preferred feedstock for hydrogen production. Direct thermal splitting of methane offers the cleanest technique to produce hydrogen and carbon as coproduct fuel. Carbonaceous catalysts have significant impact on methane to hydrogen conversion. This study presents thermogravimetric experiment results of carbon-catalyzed methane decomposition using commercial catalyst. Results are presented in terms of carbon formation rate, amount of carbon deposition on the catalyst, sustainability factor, catalyst activity, and kinetics of the reaction. The results show that weight gain because of carbon formation depends on reaction temperature, methane volume percent in the feed gas, and nature of the carbonaceous catalyst. It was observed that the reaction rate was dominant at the beginning, and deactivation rate was dominant toward the end of reaction. X-ray diffraction (XRD) and scanning electron microscopic (SEM) analysis of deactivated catalytic samples show decreasing disorder with increasing reaction temperature. Finally, performance comparison of activated carbons (ACs) studied in literature shows that activated carbon sample chosen in this study outperforms in terms of carbon deposition, reaction rate, carbon weight gain, and sustainability factor.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleHydrogen Production by Carbon-Catalyzed Methane Decomposition Via Thermogravimetry
    typeJournal Paper
    journal volume139
    journal issue1
    journal titleJournal of Energy Resources Technology
    identifier doi10.1115/1.4035145
    journal fristpage12005
    journal lastpage012005-8
    treeJournal of Energy Resources Technology:;2017:;volume( 139 ):;issue: 001
    contenttypeFulltext
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