Literature DB >> 18828580

An experimental and kinetic modeling study of the oxidation of the four isomers of butanol.

Jeffrey T Moss1, Andrew M Berkowitz, Matthew A Oehlschlaeger, Joffrey Biet, Valérie Warth, Pierre-Alexandre Glaude, Frédérique Battin-Leclerc.   

Abstract

Butanol, an alcohol which can be produced from biomass sources, has received recent interest as an alternative to gasoline for use in spark ignition engines and as a possible blending compound with fossil diesel or biodiesel. Therefore, the autoignition of the four isomers of butanol (1-butanol, 2-butanol, iso-butanol, and tert-butanol) has been experimentally studied at high temperatures in a shock tube, and a kinetic mechanism for description of their high-temperature oxidation has been developed. Ignition delay times for butanol/oxygen/argon mixtures have been measured behind reflected shock waves at temperatures and pressures ranging from approximately 1200 to 1800 K and 1 to 4 bar. Electronically excited OH emission and pressure measurements were used to determine ignition-delay times. The influence of temperature, pressure, and mixture composition on ignition delay has been characterized. A detailed kinetic mechanism has been developed to describe the oxidation of the butanol isomers and validated by comparison to the shock-tube measurements. Reaction flux and sensitivity analysis illustrates the relative importance of the three competing classes of consumption reactions during the oxidation of the four butanol isomers: dehydration, unimolecular decomposition, and H-atom abstraction. Kinetic modeling indicates that the consumption of 1-butanol and iso-butanol, the most reactive isomers, takes place primarily by H-atom abstraction resulting in the formation of radicals, the decomposition of which yields highly reactive branching agents, H atoms and OH radicals. Conversely, the consumption of tert-butanol and 2-butanol, the least reactive isomers, takes place primarily via dehydration, resulting in the formation of alkenes, which lead to resonance stabilized radicals with very low reactivity. To our knowledge, the ignition-delay measurements and oxidation mechanism presented here for 2-butanol, iso-butanol, and tert-butanol are the first of their kind.

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Year:  2008        PMID: 18828580     DOI: 10.1021/jp806464p

Source DB:  PubMed          Journal:  J Phys Chem A        ISSN: 1089-5639            Impact factor:   2.781


  6 in total

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2.  PROGRESS IN DETAILED KINETIC MODELING OF THE COMBUSTION OF OXYGENATED COMPONENTS OF BIOFUELS.

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4.  The kinetic model of cyclohexene-air combustion over a wide temperature range.

Authors:  Hongbiao Lu; Wenhui Kong; Changhua Zhang; Jingbo Wang; Xiangyuan Li
Journal:  RSC Adv       Date:  2021-12-15       Impact factor: 4.036

5.  Shock tube and chemical kinetic modeling study of the oxidation of 2,5-dimethylfuran.

Authors:  Baptiste Sirjean; René Fournet; Pierre-Alexandre Glaude; Frédérique Battin-Leclerc; Weijing Wang; Matthew A Oehlschlaeger
Journal:  J Phys Chem A       Date:  2013-01-31       Impact factor: 2.781

6.  Computational Studies on the Thermodynamic and Kinetic Parameters of Oxidation of 2-Methoxyethanol Biofuel via H-Atom Abstraction by Methyl Radical.

Authors:  Mohamed A Abdel-Rahman; Tarek M El-Gogary; Nessreen Al-Hashimi; Mohamed F Shibl; Kazunari Yoshizawa; Ahmed M El-Nahas
Journal:  Sci Rep       Date:  2019-10-25       Impact factor: 4.379

  6 in total

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