二元活性剂对氨高温自着火特性影响分析

Analysis of the Influence of Binary Activators on the High-temperature Self-ignition Characteristics of Ammonia

来源:中文会议(科协)
中文摘要英文摘要

在全球碳中和的背景下,氨作为可再生无碳燃料受到广泛关注。文章利用激波管实验平台测量了氨、氨/氢、氨/氢/二甲醚三种燃料在当量比为1.0,压力为0.14 MPa、1.0 MPa 下的高温着火延迟期,并构建了适用于高温点火的氨/氢/二甲醚动力学模型。实验结果表明,氨/氢/二甲醚三元混合燃料相比于氨/氢二元混合燃料在相同条件下有着更短的着火延迟期,其在1.0 MPA 时,含5%H2+5%DME 活性剂的混合燃料相比与0.14 MPa 时的纯氨,IDT 缩短了近45 倍。动力学分析表明,该三元混合燃料有着更低的临界自燃温度,有利于在压燃式内燃机上的应用,DME 和H2 在早期氧化过程中产生了大量的活性自由基并活化了自由基池是其拥有更高反应性的关键。

In the context of global carbon neutrality, ammonia has received widespread attention as a renewable and carbon-free fuel. The study utilized a shock tube experimental platform to measure the high-temperature ignition delay time of ammonia, ammonia/hydrogen, and ammonia/hydrogen/dimethyl ether (DME) fuels at an equivalence ratio of 1.0 and pressures of 0.14 MPa and 1.0 MPa. Additionally, a kinetic model suitable for high-temperature ignition of ammonia/hydrogen/DME was constructed. Experimental results indicate that the ternary mixture of ammonia/hydrogen/DME exhibits shorter ignition delay periods compared to the binary mixture of ammonia/hydrogen under the same conditions. Specifically, at 1.0 MPa, the ignition delay time (IDT) of the mixed fuel containing 5% H2 and 5% DME is reduced by nearly 45 times compared to pure ammonia at 0.14 MPa. Kinetic analysis reveals that the ternary mixture has a lower spontaneous ignition temperature, making it favorable for application in compression-ignition internal combustion engines. The key factors contributing to its higher reactivity are the significant generation of reactive radicals from DME and H2 during the early oxidation process, which activate the radical pool.

褚祥林;陈皓;马志豪;王鑫;

河南科技大学 车辆与交通工程学院,洛阳 471003;河南科技大学 车辆与交通工程学院,洛阳 471003;河南科技大学 车辆与交通工程学院,洛阳 471003;河南科技大学 车辆与交通工程学院,洛阳 471003;

内燃动力碳中和与排放控制2023学术年会

TK401

二甲醚 着火延迟期 化学动力学

ammonia hydrogen dimethyl ether ignition delay time chemical kinetics

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