1. Study on combustion performance and reaction mechanisms of ammonia blended with low-carbon alkanes.
- Author
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Zhang, Siqi, Yue, Wanying, Zhang, Bin, Xia, Yuanchen, Wang, Boqiao, and Zhang, Jinnan
- Subjects
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ALKANE analysis , *RADICALS (Chemistry) , *DEHYDROGENATION , *NUMERICAL analysis , *ALKANES - Abstract
This study elucidates the impact of the types and blending ratios of low-carbon alkanes (methane and ethane, C1/C2) on the combustion and emission performance of NH₃ and analyzes the reasons for the differences in the effects of C1/C2 from the elementary reaction. The experimental and numerical analysis results show that C1/C2 reduces the temperature dependence of NH₃ oxidation and promotes the formation of combustion-promoting (CP) radicals. The concentration of CP is determined by the strength of the H-abstraction reactions of C1/C2. The initial H-abstraction product of C1, CH₃, exhibits reaction inertness, whereas the inert radicals of C2 (C₂H₄, C₂H₃, and C₂H₂) appear after three main H-abstraction steps. Additionally, C1/C2 intensifies the NH→N→NO reaction, worsening thermal-NO emissions; this study classifies it as a thermal-NO generation pathway. Although NH₂ and NH significantly reduce fuel-NO, their effect on thermal-NO is less pronounced. The consumption of thermal-NO primarily depends on the reverse direction of the reaction N 2 +O N + NO. • The introduction of C1/C2 reduces the temperature dependence of NH 3 oxidation reactions. • The dehydrogenation reactions of C1/C2 produce different types of inert radicals that limit subsequent dehydrogenation reactions. • C1's inert radicals form after the first dehydrogenation, while C2's form after the third dehydrogenation. • For the HC(O)/NH 3 , NH.→N→NO should be classified as one of the thermal-NO generation pathways. • Thermal-NO consumption depends on N accumulation, driving the reaction N 2 +O=N+NO. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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