• DocumentCode
    1676570
  • Title

    Plasma reforming of aliphatic hydrocarbons with CO2

  • Author

    Futamura, Shigeru ; Gurusamy, Annadurai

  • Author_Institution
    Nat. Inst. of Adv. Ind. Sci. & Technol., Ibaraki, Japan
  • Volume
    1
  • fYear
    2004
  • Lastpage
    586
  • Abstract
    CO2 reforming of methane, propane, and neopentane was investigated with a ferroelectric packed bed reactor in N2 at different temperatures. No chemical interaction was observed between these hydrocarbons and CO2 in nonthermal plasma, and their conversions decreased with an increase in the counterpart hydrocarbon or CO2. H2 yield also decreased with an increase in CO2 concentration. CO was formed both from CO2 and CH4, and its yield decreased with an increase in CH4 concentration. The molar ratio of H2 to CO depended on substrate hydrocarbon and reaction temperature, and decreased with increases in CO2 concentration and reactor energy density. The reactivity of the hydrocarbon decreased in the order: propane > neopentane > methane. With an increase in reaction temperature, hydrocarbon conversion and H2 yield increased. Reaction temperature controls the subsequent and thermal processes of secondary decomposition of hydrocarbon and product formation, which are induced by radicals generated in situ.
  • Keywords
    carbon compounds; chemical reactions; global warming; organic compounds; plasma applications; plasma devices; CO2; aliphatic hydrocarbons; ferroelectric packed bed reactor; hydrocarbon conversion; molar ratio; nonthermal plasma; plasma reforming; reaction temperature; reactor energy density; substrate hydrocarbon; Chemical technology; Electrodes; Ferroelectric materials; Global warming; Hydrocarbons; Inductors; Plasma applications; Plasma chemistry; Plasma properties; Plasma temperature;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Industry Applications Conference, 2004. 39th IAS Annual Meeting. Conference Record of the 2004 IEEE
  • ISSN
    0197-2618
  • Print_ISBN
    0-7803-8486-5
  • Type

    conf

  • DOI
    10.1109/IAS.2004.1348464
  • Filename
    1348464