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DOI10.1016/j.atmosenv.2019.117166
Atmospheric oxidation of C10~14 n-alkanes initiated by Cl atoms: Kinetics and mechanism
Shi B.; Wang W.; Zhou L.; Sun Z.; Fan C.; Chen Y.; Zhang W.; Qiao Y.; Qiao Y.; Ge M.
发表日期2020
ISSN1352-2310
卷号222
英文摘要The Cl-initiated photo-oxidation reactions of n-alkanes: C10~C14, were investigated by using Proton-Transfer-Reaction Mass Spectrometry in the smog chamber, and the present work provided the kinetic parameters of the reactions of Cl atoms with C11~14 n-alkanes for the first time. The rate constants (in units of cm3molecule−1s−1) were obtained using relative rate method with trans-2-butene, m-xylene and ethylbenzene as references at (298 ± 1)K and 760 Torr were k(n-decane)=(4.82 ± 0.32) × 10−10, k(n-undecane)=(5.02 ± 0.33) × 10−10, k(n-dodecane)=(5.12 ± 0.29) × 10−10, k(n-tridecane)=(5.30 ± 0.30) × 10−10, k(n-tetradecane)=(5.68 ± 0.34) × 10−10, respectively. The measured rate constants have also been used to calculate tropospheric lifetimes of these compounds (C10, C11, C12, C13, C14), which were 11.5, 11.1, 10.9 10.5 and 9.8 h for each n-alkane. In addition, the gas-phase photooxidation products of the reactions were also measured. Based on the obtained results, the reaction mechanisms of Cl atoms with these five alkanes were proposed. © 2019 Elsevier Ltd
关键词Cl atomsn-AlkanePhotooxidation reactionRate constantsSmog chamber
语种英语
scopus关键词Air pollution; Atoms; Chlorine; Mass spectrometry; Photooxidation; Proton transfer; Rate constants; Atmospheric oxidation; Cl atoms; Kinetics and mechanism; n-Alkanes; Proton-transfer reaction mass spectrometries; Relative rate method; Smog chambers; Tropospheric lifetime; Paraffins; alkane; carbon 14; chlorine; ethylbenzene; alkane; chemical reaction; chlorine; kinetics; oxidation; photooxidation; smog; atmosphere; atom; controlled study; kinetic isotope effect; kinetic parameters; limit of detection; photolysis; photooxidation; priority journal; proton transfer reaction mass spectrometry; rate constant; reaction analysis; room temperature; smog; ultraviolet radiation
来源期刊ATMOSPHERIC ENVIRONMENT
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/249455
作者单位State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China; University of Chinese Academy of Sciences, Beijing, 100049, China; Center for Excellence in Regional Atmospheric Environment, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, China; College of Chemistry and Material Science, Hebei Normal University, Road East of 2nd Ring South, Shijiazhuang, 050024, China; National Engineering Research Center for Flue Gas Desulfurization, Department of Environmental Science and Engineering, Sichuan University, Chengdu, 610065, China
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Shi B.,Wang W.,Zhou L.,et al. Atmospheric oxidation of C10~14 n-alkanes initiated by Cl atoms: Kinetics and mechanism[J],2020,222.
APA Shi B..,Wang W..,Zhou L..,Sun Z..,Fan C..,...&Ge M..(2020).Atmospheric oxidation of C10~14 n-alkanes initiated by Cl atoms: Kinetics and mechanism.ATMOSPHERIC ENVIRONMENT,222.
MLA Shi B.,et al."Atmospheric oxidation of C10~14 n-alkanes initiated by Cl atoms: Kinetics and mechanism".ATMOSPHERIC ENVIRONMENT 222(2020).
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