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DOI10.1126/science.1112532
Chemistry: Enols are common intermediates in hydrocarbon oxidation
Taatjes C.A.; Hansen N.; McIlroy A.; Miller J.A.; Senosiain J.P.; Klippenstein S.J.; Qi F.; Sheng L.; Zhang Y.; Cool T.A.; Wang J.; Westmoreland P.R.; Law M.E.; Kasper T.; Kohse-Höinghaus K.
发表日期2005
ISSN0036-8075
起始页码1887
结束页码1889
卷号308期号:5730
英文摘要Models for chemical mechanisms of hydrocarbon oxidation rely on spectrometric identification of molecular structures in flames. Carbonyl (keto) compounds are well-established combustion intermediates. However, their less-stable enol tautomers, bearing OH groups adjacent to carbon-carbon double bonds, are not included in standard models. We observed substantial quantities of two-, three-, and four-carbon enols by photoionization mass spectrometry of flames burning representative compounds from modern fuel blends. Concentration profiles demonstrate that enol flame chemistry cannot be accounted for purely by keto-enol tautomerization. Currently accepted hydrocarbon oxidation mechanisms will likely require revision to explain the formation and reactivity of these unexpected compounds.
英文关键词Alcohols; Flame research; Mathematical models; Molecular structure; Oxidation; Photoionization; Spectrometers; Double bonds; Enols; Flame chemistry; Tautomers; Hydrocarbons; hydrocarbon; chemistry; article; chemical analysis; chemical bond; chemical structure; combustion; concentration (parameters); mass spectrometry; molecular mechanics; molecular stability; oxidation; priority journal; reaction analysis; structure analysis
语种英语
来源期刊Science
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/245700
作者单位Combustion Research Facility, Mail Stop 9055, Sandia National Laboratories, Livermore, CA 94551-0969, United States; JILA, National Institute of Standards and Technology, University of Colorado, Boulder, CO 80309-0440, United States; National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui 230026, China; School of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853, United States; Department of Chemical Engineering, University of Massachusetts, Amherst, MA 01003-9303, United States; Physikalische Chemie I, Universität Bielefeld, Universitätsstraße 25, 33615 Bielefeld, Germany
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Taatjes C.A.,Hansen N.,McIlroy A.,et al. Chemistry: Enols are common intermediates in hydrocarbon oxidation[J],2005,308(5730).
APA Taatjes C.A..,Hansen N..,McIlroy A..,Miller J.A..,Senosiain J.P..,...&Kohse-Höinghaus K..(2005).Chemistry: Enols are common intermediates in hydrocarbon oxidation.Science,308(5730).
MLA Taatjes C.A.,et al."Chemistry: Enols are common intermediates in hydrocarbon oxidation".Science 308.5730(2005).
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