TY - JOUR
T1 - A shock tube study of the ignition delay time of DME/ammonia mixtures
T2 - Effect of fuel blending from high temperatures to the NTC regime
AU - Jiang, Xue
AU - Zhang, Qiying
AU - Liu, Xiyu
AU - Zhang, Tianqi
AU - Zhang, Yingjia
AU - Huang, Zuohua
AU - Deng, Fuquan
AU - Zhao, Ningbo
AU - Zheng, Hongtao
AU - Yan, Yingwen
N1 - Publisher Copyright:
© 2024
PY - 2024/7/1
Y1 - 2024/7/1
N2 - An experimental and chemical kinetic investigation has been conducted to understand the effect of dimethyl ether (DME) blending on the ignition delay time of ammonia (NH3) from high temperatures to the negative temperature coefficient (NTC) regime in a shock tube with the DME fractions of 0 %, 5 %, 25 %, 50 %, and 100 %, temperatures of 690–1810 K, pressures of 1.2 and 10 atm, and equivalence ratio of 1.0. Four representative literature chemical kinetic models were validated against our measurements, however none of the above models can provide reasonable predictions of the experimental data in the NTC regime. A chemical kinetic model was developed in this study, the model was also been validated by the ignition delay times, laminar flame speeds and specie profiles data of DME/ammonia mixtures in the literature. Experimental results show that the ignition delay times of NH3 can be obviously shorten by 5 % DME addition in both high temperature and the NTC region. Chemical kinetic analyses reveal that the addition of 5 % DME can rapidly generate OH radical through the reaction pathway of HO2 → H2O2 → OH at 1250 K. At 800 K, the blended DME can be rapidly consumed via the reaction pathway of R → RO2 → QOOH → OOQOOH to promote the production of OH radical in the early stage, thus lead to the reduced ignition delay time of DME/NH3 mixture.
AB - An experimental and chemical kinetic investigation has been conducted to understand the effect of dimethyl ether (DME) blending on the ignition delay time of ammonia (NH3) from high temperatures to the negative temperature coefficient (NTC) regime in a shock tube with the DME fractions of 0 %, 5 %, 25 %, 50 %, and 100 %, temperatures of 690–1810 K, pressures of 1.2 and 10 atm, and equivalence ratio of 1.0. Four representative literature chemical kinetic models were validated against our measurements, however none of the above models can provide reasonable predictions of the experimental data in the NTC regime. A chemical kinetic model was developed in this study, the model was also been validated by the ignition delay times, laminar flame speeds and specie profiles data of DME/ammonia mixtures in the literature. Experimental results show that the ignition delay times of NH3 can be obviously shorten by 5 % DME addition in both high temperature and the NTC region. Chemical kinetic analyses reveal that the addition of 5 % DME can rapidly generate OH radical through the reaction pathway of HO2 → H2O2 → OH at 1250 K. At 800 K, the blended DME can be rapidly consumed via the reaction pathway of R → RO2 → QOOH → OOQOOH to promote the production of OH radical in the early stage, thus lead to the reduced ignition delay time of DME/NH3 mixture.
KW - Ammonia
KW - Chemical kinetic
KW - DME
KW - Ignition delay time
UR - https://www.scopus.com/pages/publications/85187196851
U2 - 10.1016/j.fuel.2024.131426
DO - 10.1016/j.fuel.2024.131426
M3 - 文章
AN - SCOPUS:85187196851
SN - 0016-2361
VL - 367
JO - Fuel
JF - Fuel
M1 - 131426
ER -