Study of the Low Temperature Oxidation of Propane

被引:59
作者
Cord, Maximilien [1 ]
Husson, Benoit [1 ]
Lizardo Huerta, Juan Carlos [1 ]
Herbinet, Olivier [1 ]
Glaude, Pierre-Alexandre [1 ]
Fournet, Rene [1 ]
Sirjean, Baptiste [1 ]
Battin-Leclerc, Frederique [1 ]
Ruiz-Lopez, Manuel [2 ]
Wang, Zhandong [3 ]
Xie, Mingfeng [3 ]
Cheng, Zhanjun [3 ]
Qi, Fei [3 ]
机构
[1] Univ Lorraine, Lab React & Genie Proc, CNRS, ENSIC, F-54000 Nancy, France
[2] Univ Lorraine, Lab Struct & Reactivite Syst Mol Complexes, CNRS, F-54506 Vandoeuvre Les Nancy, France
[3] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
关键词
GAS-PHASE OXIDATION; REACTION-KINETICS; ACETIC-ACID; PLUS O-2; PHOTOIONIZATION; COMBUSTION; RADICALS; MECHANISMS; PHOTOABSORPTION; AUTOIGNITION;
D O I
10.1021/jp309821z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The low-temperature oxidation of propane was investigated using a jet-stirred reactor at atmospheric pressure and two methods of analysis: gas chromatography and synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS) with direct sampling through a molecular jet. The second method allowed the identification of products, such as molecules with hydroperoxy functions, which are not stable enough to be detected by gas chromatography. Mole fractions of the reactants and reaction products were measured as a function of the temperature (530-730 K), with a particular attention to reaction products involved in the low temperature oxidation, such as cyclic ethers, aldehydes, alcohols, ketones, and hydroperoxides. A new model has been obtained from an automatically generated one, which was used as a starting point, with a large number of re-estimated thermochemical and kinetic data. The kinetic data of the most sensitive reactions, i.e., isomerizations of alkylperoxy radicals and the subsequent decompositions, have been calculated at the CBS-QB3 level of theory. The model allows a satisfactory prediction of the experimental data. A flow rate analysis has allowed highlighting the important reaction channels.
引用
收藏
页码:12214 / 12228
页数:15
相关论文
共 55 条
[11]   Progress toward a unified detailed kinetic model for the autoignition of alkanes from C4 to C10 between 600 and 1200 K [J].
Buda, F ;
Bounaceur, R ;
Warth, V ;
Glaude, P ;
Fournet, R ;
Battin-Leclerc, F .
COMBUSTION AND FLAME, 2005, 142 (1-2) :170-186
[12]   High-resolution photoabsorption and photoionization spectra of C2H4 and C2D4 [J].
Chen, FZ ;
Wu, CYR .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 1999, 32 (13) :3283-3293
[13]   Photoionization mass spectrometer for studies of flame chemistry with a synchrotron light source [J].
Cool, TA ;
McIlroy, A ;
Qi, F ;
Westmoreland, PR ;
Poisson, L ;
Peterka, DS ;
Ahmed, M .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2005, 76 (09)
[14]   Selective detection of isomers with photoionization mass spectrometry for studies of hydrocarbon flame chemistry [J].
Cool, TA ;
Nakajima, K ;
Mostefaoui, TA ;
Qi, F ;
McIlroy, A ;
Westmoreland, PR ;
Law, ME ;
Poisson, L ;
Peterka, DS ;
Ahmed, M .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (16) :8356-8365
[15]   Absolute photoabsorption and photoionization of formaldehyde in the VUV and soft X-ray regions (3-200 eV) [J].
Cooper, G ;
Anderson, JE ;
Brion, CE .
CHEMICAL PHYSICS, 1996, 209 (01) :61-77
[16]   Improvement of the Modeling of the Low-Temperature Oxidation of n-Butane: Study of the Primary Reactions [J].
Cord, Maximilien ;
Sirjean, Baptiste ;
Fournet, Rene ;
Tomlin, Alison ;
Ruiz-Lopez, Manuel ;
Battin-Leclerc, Frederique .
JOURNAL OF PHYSICAL CHEMISTRY A, 2012, 116 (24) :6142-6158
[17]   Temperature dependence and deuterium kinetic isotope effects in the HCO(DCO)+O2 reaction between 296 and 673 K [J].
DeSain, JD ;
Jusinski, LE ;
Ho, AD ;
Taatjes, CA .
CHEMICAL PHYSICS LETTERS, 2001, 347 (1-3) :79-86
[18]   Measurements, theory, and modeling of OH formation in ethyl plus O2 and propyl plus O2 reactions [J].
DeSain, JD ;
Klippenstein, SJ ;
Miller, JA ;
Taatjes, CA .
JOURNAL OF PHYSICAL CHEMISTRY A, 2003, 107 (22) :4415-4427
[19]   THEORETICAL INVESTIGATION OF COMPETING MECHANISMS IN THE THERMAL UNIMOLECULAR DECOMPOSITION OF ACETIC-ACID AND THE HYDRATION REACTION OF KETENE [J].
DUAN, XF ;
PAGE, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (18) :5114-5119
[20]   The penetration of a potential barrier by electrons [J].
Eckart, C .
PHYSICAL REVIEW, 1930, 35 (11) :1303-1309