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
Link To Document :
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