Optimization of the full-load combustion schemes of n-butanol/biodiesel reactivity-controlled compression ignition (RCCI) toward high-efficiency and low-emission engines

生物柴油 点火系统 燃烧 柴油 均质压燃 环境科学 正丁醇 汽车工程 丁醇 生物燃料 氮氧化物 工艺工程 材料科学 废物管理 化学 热力学 工程类 燃烧室 物理 有机化学 催化作用 乙醇
作者
Yikang Cai,Ming Jia,Yaopeng Li,Haoran Li,Zihe Liu,Rui Ding,Xingcai Lü
出处
期刊:International Journal of Engine Research [SAGE Publishing]
卷期号:26 (4): 472-497 被引量:6
标识
DOI:10.1177/14680874241278960
摘要

Biodiesel and n-butanol, as popular alternative fuels, can be used in advanced reactivity-controlled compression ignition (RCCI) engines for efficient and clean combustion. However, the complex interactions between n-butanol and biodiesel, as well as the best combustion schemes at different loads, remain poorly understood. Given this, the objective of this paper is to identify optimal fuel organizations for n-butanol/biodiesel RCCI engines across different load scenarios by combining engine simulation with a global optimization algorithm, explore the potential synergies of control parameters, and analyze microscopic dual-fuel interactions based on the integrated average reaction path analysis. Results show that the optimal scheme at low load employs almost homogeneous fuel-air mixtures at elevated temperature atmosphere above 390 K, with n-butanol energy share exceeding 96% and optimal biodiesel injection timing between −70 and −50 °CA. Higher n-butanol ratio coupled with increased intake temperature improves engine performance. For mid load, biodiesel injection timing is retarded to −55 to −30 °CA, and biodiesel proportion is increased to introduce reactivity stratification, while maintaining its energy share below 20% to mitigate NO x emissions. Notably, biodiesel density is identified as the primary physical property influencing NO x formation. At high load, a split combustion scheme involving premixing and subsequent diffusion combustion is optimal. The physical effects of n-butanol addition minimally impact the low-temperature ignition of biodiesel, while its chemical effects significantly defer the low-temperature reactivity. The reaction path analysis reveals that n-butanol competes with biodiesel for OH radical consumption, with a large proportion of OH and HO 2 consumed in the cyclic reactions of nC 4 H 9 OH and nC 4 H 8 OH. Adjusting the reactivity stratification affects the reaction state of n-butanol entrained by the biodiesel jets. Higher reactivity gradient intensifies biodiesel reactions to induce the pyrolysis of the involved n-butanol through nC 4 H 8 OH => 2C 2 H 4 + OH, therefore resulting in more staged heat release.
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