Ethylene pyrolysis and the subsequent molecular weight growth reactions

Inyong Kang, Ahmed Al Shoaibi, Anthony M. Dean

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

Abstract

This study focuses on the pyrolysis and molecular weight growth reactions of ethylene under conditions relevant to reformer or SOFC operation (τ=1-5s, T=550∼900°C, P-0.8 atm). Ethylene was chosen since it is often the dominant olefin formed during hydrocarbon pyrolysis, and it is also known to lead to deposit formation. Ethylene conversions were observed to vary substantially over the range of conditions used. The major light products observed were H2, CH4, C2H2, C3H6, C4H6, and heavier species. The most abundant aromatic species observed were benzene and styrene. Although it appears that current kinetic model can properly account for the initial conversion of ethylene to butadiene, the prediction of other product distributions is not satisfactory. The overprediction of 1,3 butadiene is likely due to the fact that reactions of butadiene to form higher molecular weight products are too slow in the model.

Original languageBritish English
Title of host publicationAmerican Chemical Society - 237th National Meeting and Exposition, ACS 2009, Abstracts of Scientific Papers
StatePublished - 2009
Event237th National Meeting and Exposition of the American Chemical Society, ACS 2009 - Salt Lake City, UT, United States
Duration: 22 Mar 200926 Mar 2009

Publication series

NameACS National Meeting Book of Abstracts
ISSN (Print)0065-7727

Conference

Conference237th National Meeting and Exposition of the American Chemical Society, ACS 2009
Country/TerritoryUnited States
CitySalt Lake City, UT
Period22/03/0926/03/09

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