A comprehensive experimental and kinetic modeling study of di-isobutylene isomers: Part 2

被引:10
作者
Lokachari, Nitin [1 ]
Kukkadapu, Goutham [2 ]
Etz, Brian D. [3 ]
Fioroni, Gina M. [3 ]
Kim, Seonah [3 ,4 ]
Steglich, Mathias [5 ]
Bodi, Andras [5 ]
Hemberger, Patrick [5 ]
Matveev, Sergey S. [6 ]
Thomas, Anna [3 ]
Song, Hwasup [7 ,9 ]
Vanhove, Guillaume [7 ]
Zhang, Kuiwen [2 ]
Dayma, Guillaume [8 ]
Lailliau, Maxence [8 ]
Serinyel, Zeynep [8 ]
Konnov, Alexander A. [10 ]
Dagaut, Philippe [8 ]
Pitz, William J.
Curran, Henry J. [1 ]
机构
[1] Univ Galway, Ryan Inst, Combust Chem Ctr, Sch Biol & Chem Sci,MaREI, Galway, Ireland
[2] Lawrence Livermore Natl Lab, Livermore, CA 94551 USA
[3] Natl Renewable Energy Lab, Golden, CO 80401 USA
[4] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
[5] Paul Scherrer Inst, Lab Femtochem & Synchrotron Radiat, CH-5232 Villigen, Switzerland
[6] Samara Natl Res Univ, Sci & Educ Ctr Fluid Dynam Res, Samara, Russia
[7] Univ Lille, CNRS, UMR 8522, PC2A Physicochim Proc Combust & Atmosphere, Lille F-59000, France
[8] CNRS INSIS, Inst Combust Aerotherm React & Environm, Orleans, France
[9] Kumoh Natl Inst Technol, Dept Mech Engn, 61 Daehak ro, Gumi 39177, Gyeongsangbuk D, South Korea
[10] Lund Univ, Div Combust Phys, Lund, Sweden
基金
俄罗斯科学基金会; 爱尔兰科学基金会;
关键词
Di-isobutylene; Pyrolysis; ignition delay; Burning velocity; Kinetic modeling; ACTIVE THERMOCHEMICAL TABLES; LAMINAR BURNING VELOCITIES; COMPOUND METHODS CBS-QB3; SHOCK-TUBE MEASUREMENTS; ADDITION-REACTIONS; H ABSTRACTION; CBS-APNO; OH; RADICALS; IGNITION;
D O I
10.1016/j.combustflame.2022.112547
中图分类号
O414.1 [热力学];
学科分类号
摘要
A wide variety of high temperature experimental data obtained in this study complement the data on the oxidation of the two di-isobutylene isomers presented in Part I and offers a basis for an extensive validation of the kinetic model developed in this study. Due to the increasing importance of unimolecular decomposition reactions in high-temperature combustion, we have investigated the di-isobutylene isomers in high dilution utilizing a pyrolysis microflow reactor and detected radical intermediates and stable products using vacuum ultraviolet (VUV) synchrotron radiation and photoelectron photoion coincidence (PEPICO) spectroscopy. Additional speciation data at oxidative conditions were also recorded utilizing a plug flow reactor at atmospheric pressure in the temperature range 725-1150 K at equivalence ratios of 1.0 and 3.0 and at residence times of 0.35 s and 0.22 s, respectively. Combustion products were analyzed using gas chromatography (GC) and mass spectrometry (MS). Ignition delay time measurements for di-isobutylene were performed at pressures of 15 and 30 bar at equivalence ratios of 0.5, 1.0, and 2.0 diluted in air in the temperature range 900-1400 K using a high-pressure shock-tube facility. New measurements of the laminar burning velocities of di-isobutylene/air flames are also presented. The experiments were performed using the heat flux method at atmospheric pressure and initial temperatures of 298-358 K. Moreover, data consistency was assessed with the help of analysis of the temperature and pressure dependencies of laminar burning velocity measurements, which was interpreted using an empirical power-law expression. Electronic structure calculations were performed to compute the energy barriers to the formation of many of the product species formed. The predictions of the present mechanism were found to be in adequate agreement with the wide variety of experimental measurements performed. (c) 2022 The Author(s). Published by Elsevier Inc. on behalf of The Combustion Institute. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ )
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页数:18
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