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Pulverized coal combustion: Fuel nitrogen mechanisms in the rich post-flame.

机译:煤粉燃烧:富燃后火焰中的燃料氮机制。

摘要

Chemical kinetic mechanisms governing the fate of coal nitrogen in the fuel-rich stage of a pulverized-coal staged combustion process were investigated. Emphasis was on determination of the effects of coal rank, temperature and stoichiometric ratios on the speciation and rates of destruction of nitrogenous species and correlation of coal data by a unif1ed mechanism. The relative importance of homogeneous and heterogeneous mechanisms during post-flame interconversion reactions of the fuel nitrogen pool was quantified. Experiments with doped propane gas and a high- and low-grade coals, burned under a variety of conditions in a 2 Kg/h downflow combustor, yielded timeresolved profiles of temperature, major (H₂, CO, CO₂, O₂ and N₂), nitrogenous (NO, HeN and NH₃) and hydrocarbon (CH₄ and C₂H₂) species. These profiles allowed global mechanisms describing the speciation and destruction of fuel nitrogen species to be explored, using predictive models of increasing levels of sophistication. Fuel nitrogen speciation varied significantly from coal to coal and depended on stoichiometric ratio and temperature, which were varied independently. A general correlation describing the destruction rate of NO was derived from data. This rate, which was first-order in both NO and NH₃, was generally valid for all coals and all conditions examined. Fuel nitrogen interconversion reactions, especially destruction of NO and HeN, was predominantly homogeneous, but no single elementary reaction was controlling. Temperature quench down the combustor is the origin of OH equilibrium overshoot. Expressions for estimating the OH equilibrium overshoot as a function of the axial temperature decay along the combustor were derived both empirically and kinetically from fundamental considerations using data from doped propane gas runs. These expressions, together with available literature values of gas phase rate coefficients, could adequately describe the post-flame NO and HeN profiles of coal and gas runs. HeN profiles in the far postflame zone of the coal flames are strongly influenced by the slow release of nitrogen from the coal residue. This devolatilization plays a critical role in supplying the HeN that drives the multistep process converting fuel N into molecular nitrogen.
机译:研究了粉煤分级燃烧过程中富燃料阶段控制煤氮命运的化学动力学机理。重点是通过统一的方法确定煤级,温度和化学计量比对含氮物质的形态和破坏率以及煤数据的相关性的影响。量化了燃料氮池的火焰后相互转化反应期间同质和异质机制的相对重要性。用掺杂的丙烷气体和高,低级煤进行实验,在各种条件下在2 Kg / h的下行流燃烧器中燃烧,得到时间分辨的温度曲线,主要温度(H 2,CO,CO 2,O 2和N 2),含氮(NO,HeN和NH 3)和烃(CH 3和C 2 H 2)物质。这些概况允许使用复杂程度不断提高的预测模型探索描述燃料氮物种形成和破坏的全球机制。煤之间的燃料氮形态差异很大,并且取决于化学计量比和温度,而化学计量比和温度是独立变化的。从数据中得出描述NO破坏率的一般相关性。该速率在NO和NH3中都是一阶的,通常对所有煤和所有条件都有效。燃料氮的相互转化反应,尤其是NO和HeN的破坏,基本上是均相的,但没有一个单元素反应受到控制。燃烧器的温度骤冷是OH平衡过冲的根源。使用掺杂的丙烷气运行数据,从基本考虑中,从经验和动力学上推导了根据燃烧室的轴向温度衰减来估计OH平衡过冲的表达式。这些表达式以及可用的气相速率系数文献值可以充分描述燃煤和天然气管道的火焰后NO和HeN曲线。从煤渣中缓慢释放出氮气会严重影响煤火焰远处的HeN分布。这种脱挥发分在提供HeN方面起着关键作用,该HeN驱动着将燃料N转化为分子氮的多步过程。

著录项

  • 作者

    Bose Arun Chand.;

  • 作者单位
  • 年度 1989
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类

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