Detailed chemical kinetic modeling of the effects of C=C double bonds on the ignition of biodiesel fuels

被引:75
作者
Westbrook, C. K. [1 ]
Pitz, W. J. [1 ]
Sarathy, S. M. [1 ]
Mehl, M. [1 ]
机构
[1] Lawrence Livermore Natl Lab, Phys & Life Sci Directorate, Livermore, CA 94551 USA
关键词
Reaction mechanisms; Ignition; Diesel engines; Biodiesel fuels; N-HEPTANE; REACTION-MECHANISM; METHYL OLEATE; SHOCK-TUBE; COMBUSTION; OXIDATION; HYDROCARBONS; AUTOIGNITION; TEMPERATURE;
D O I
10.1016/j.proci.2012.05.025
中图分类号
O414.1 [热力学];
学科分类号
摘要
A detailed chemical kinetic reaction mechanism previously developed to study combustion of soy and rapeseed oil methyl ester biodiesel fuels is used to simulate combustion of many other biodiesel fuels derived from different vegetable oils and animal fats. All of these biodiesel fuels consist of unique mixtures of the same five individual, single-component methyl esters, including methyl stearate, methyl oleate, methyl linoleate, methyl linolenate, and methyl palmitate. The stearate and palmitate molecules are saturated, while the oleate, linoleate and linolenate have one, two and three C=C double bonds, respectively. Each plant-or fat-derived biodiesel fuel that is made from the same five components has variations in combustion properties that depend on differences in the relative fractions of these five components. The present study focuses on ignition properties of these oil-and fat-derived biodiesel fuels and on their cetane numbers (CN), which measure relative ignition rates under diesel engine operating conditions. A key factor determining differences in ignition properties and CN of the many methyl ester diesel fuels is shown to be the number of C=C double bonds in the long carbon chains of each component molecule, with each C=C double bond reducing the CN value by a significant amount. Each C=C double bond provides allylic sites where H atoms are easily abstracted, but these allylic radical sites are shown to be weak bonding sites for molecular oxygen that do not support subsequent isomerization reactions that lead to low temperature reactivity and ignition. This reduced rate of low temperature reactivity is responsible for the reductions in CN due to the presence of these C=C double bonds. The amount of reduction in low temperature reactivity is roughly proportional to the number of C=C double bonds in each biodiesel fuel molecule, relative to the saturated components of biodiesel fuel. (C) 2012 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:3049 / 3056
页数:8
相关论文
共 27 条
[1]  
[Anonymous], 2004, NRELSR54036805
[2]   Detailed chemical kinetic models for the low-temperature combustion of hydrocarbons with application to gasoline and diesel fuel surrogates [J].
Battin-Leclerc, F. .
PROGRESS IN ENERGY AND COMBUSTION SCIENCE, 2008, 34 (04) :440-498
[3]   Experimental study of the oxidation of methyl oleate in a jet-stirred reactor [J].
Bax, Sarah ;
Hakka, Mohammed Hichem ;
Glaude, Pierre-Alexandre ;
Herbinet, Olivier ;
Battin-Leclerc, Frederique .
COMBUSTION AND FLAME, 2010, 157 (06) :1220-1229
[4]   Effect of the Degree of Unsaturation of Biodiesel Fuels on Engine Performance, Combustion Characteristics, and Emissions [J].
Benjumea, Pedro ;
Agudelo, John R. ;
Agudelo, Andres F. .
ENERGY & FUELS, 2011, 25 (01) :77-85
[5]   Influence of the position of the double bond on the autoignition of linear alkenes at low temperature [J].
Bounaceur, R. ;
Warth, V. ;
Sirjean, B. ;
Glaude, P. A. ;
Fournet, R. ;
Battin-Leclerc, F. .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2009, 32 :387-394
[6]   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
[7]   Ignition delay times of methyl oleate and methyl linoleate behind reflected shock waves [J].
Campbell, M. F. ;
Davidson, D. F. ;
Hanson, R. K. ;
Westbrook, C. K. .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2013, 34 :419-425
[8]   SHOCK-TUBE INVESTIGATION OF SELF-IGNITION OF N-HEPTANE AIR MIXTURES UNDER ENGINE RELEVANT CONDITIONS [J].
CIEZKI, HK ;
ADOMEIT, G .
COMBUSTION AND FLAME, 1993, 93 (04) :421-433
[9]   A comprehensive modeling study of iso-octane oxidation [J].
Curran, HJ ;
Gaffuri, P ;
Pitz, WJ ;
Westbrook, CK .
COMBUSTION AND FLAME, 2002, 129 (03) :253-280
[10]   A comprehensive modeling study of n-heptane oxidation [J].
Curran, HJ ;
Gaffuri, P ;
Pitz, WJ ;
Westbrook, CK .
COMBUSTION AND FLAME, 1998, 114 (1-2) :149-177