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Kinetic modeling and experimental investigation of laminar burning velocity in 2- and 3-pentanone/ammonia premixed flames

  • Xu He
  • , Chengyuan Zhao
  • , Guangyuan Feng
  • , Xiaoran Zhou
  • , Zechang Liu*
  • , Zhi Wang
  • , Qingchu Chen
  • *此作品的通讯作者
  • Beijing Institute of Technology
  • Tsinghua University

科研成果: 期刊稿件文章同行评审

摘要

In recent years, pentanone, a biomass-derived fuel, has attracted significant attention in the field of combustion due to its excellent anti-knock properties and high energy density. To address the low reactivity inherent in ammonia (NH3) combustion, blending pentanone with NH3 has emerged as a promising strategy. This study investigates laminar burning velocities (LBVs) of 2-pentanone (nPMK)/NH3 mixtures at pressures of 1 atm and 3 atm, with a temperature of 448 K and nPMK mole fractions ranging from 0.1 to 1.0. Additionally, building upon the authors’ previous research on 3-pentanone (DEK)/NH3 mixtures, a comparative analysis was conducted to evaluate the effects of both linear pentanone isomers on NH3 flame propagation. The kinetic model utilized is an extension of an earlier pentanone-NH3 model, which has been further refined using the latest experimental data and prior research findings. The results show that blending 50 % DEK with NH3 can increase LBV by up to 350 % compared to pure NH3-air mixtures, while nPMK achieves a maximum LBV increase of 300 %, underscoring pentanone's potential to enhance NH3 combustion performance. Under stoichiometric conditions, the LBV of DEK/NH3-air mixtures is consistently 3–4 cm/s higher than that of nPMK/NH3-air mixtures, suggesting that DEK is more effective in improving NH3 combustion characteristics. Kinetic analysis reveals the difference in LBV is primarily attributable to variations in radical concentrations. Specifically, the position of the carbonyl group in each isomer results in different oxidation intermediates (i.e., CH3 for nPMK and C2H5 for DEK). In nPMK/NH3-air flames, CH3 primarily participates in the chain-terminating reaction CH3 + H(+M) = CH4(+M), consuming significant quantities of H radicals and suppressing flame propagation. In contrast, C2H5 in DEK undergo β-C–H bond scission, generating H radicals that promote flame propagation. Consequently, DEK/NH3-air mixtures exhibit higher reactivity and faster LBVs.

源语言英语
文章编号134698
期刊Fuel
390
DOI
出版状态已出版 - 15 6月 2025

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