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氨煤混燃过程中NH/煤焦/O2异相体系N氧化的分子机理
  • Title

    Molecular mechanism of N oxidation in ammonia-coal co-firing

  • 作者

    陈萍王莹汪辉春蒋博宇顾明言樊建人

  • Author

    CHEN Ping1,WANG Ying,WANG Huichun,JIANG Boyu,GU Mingyan,FAN Jianren

  • 单位

    安徽工业大学 能源与环境学院浙江大学 能源清洁利用国家重点实验室

  • Organization
    School of Energy and Environment,Anhui University of Technology;State Key Laboratory of Clean Energy Utilization,Zhe-jiang University
  • 摘要

    为了实现双碳目标,降低煤电碳排放势在必行无碳燃料氨与煤混烧被认为是降低火电碳 排放的有效途径之一而氨作为 N ,增加了氨煤混燃 NOx 排放量升高的可能性,因此,深入研究 氨煤混燃 NO 生成机理对实现氨煤混燃低碳低氮燃烧十分关键采用量子化学方法探究了当 NH3NH 形式存在时氨煤混燃 N 的氧化机理,并采用波函数分析 NH O2 在煤表面的吸附行为计 算结果表明,NH C5 表面吸附形成中间体 IM1 的过程为放热过程,放热量高达 754.79 kJ / mol,C 原子为电子供体而失电子,NH 为电子受体而得电子,促进 CN 键键合进一步探究 O2 以不同 方式吸附时 NH / 煤焦 / O2 体系的反应机理,得出 NH / 煤焦 / O2 共燃体系首先发生 NH 在煤焦表面的 氧化,随后煤焦表面残余氧或体系中O2将煤焦-N进一步氧化NH//O2异相体系中NH通过不 同反应路径生成氧化产物 NONO2 HNO,对应决速步能垒分别为 120.67323.37 193.50 kJ / mol,说明氨-N / -N 生成 NO 的过程更易进行动力学结果表明,各温度下生成 NO 的决速步 速率明显高于 NO2 ,且随着温度升高,生成 NO 的决速步速率与 HNO 的逐渐接近NH 氧化产物释 放后,残留在煤焦表面氧进一步与 C 结合成 CO 释放,实现了共燃体系氨燃料中 N 和煤粉中 C 的氧 化随后煤焦-N 与体系中 O2 发生异相氧化,实现煤焦-N NO 的转化在微观层面揭示了氨燃 烧生成 NO 过程中重要过渡产物 HNO 形成的分子机理,明晰了另一氧化产物 NO2 的生成路径,为 发展氨煤的混合燃烧机理提供理论支撑和数据参考


  • Abstract

    In order to achieve the dual carbon goals,it is imperative to reduce the carbon emissions in coal-fired power plants. Carbon-free fuel ammonia and coal co-combustion is considered to be one of the effective ways to reduce car- bon emissions from thermal power plants. Ammonia as an N source increases the possibility of increased NOx emissions from ammonia-coal co-combustion. Therefore,an in-depth study of the NO formation mechanism of ammonia-coal co- firing is very important to realize low-carbon and low-nitrogen emission of ammonia-coal co-firing. In this study,aquantum chemical method was used to explore the oxidation mechanism of N in ammonia-coal co-combustion when NH3 exists in the form of NH,and the adsorption behavior of NH and O2 on the coal surface was analyzed by wave function. The calculation results showed that the adsorption process of NH on the C5 surface to form the intermediate IM1 is a highly exothermic process with 754.79 kJ / mol. Moreover,the C atom is an electron donor and lost electrons, and the NH is an electron acceptor and obtained electrons,which promotes the C—N bond. The reaction mechanism of the NH / char / O2 system when O2 is adsorbed in different ways was further explored. It was concluded that in the NH / char / O2 co-combustion system the oxidation of NH first occurs on the char surface,and then the residual oxygen on the char surface or O2 in the system oxidizes the char-N. In the NH / coal / O2 heterogeneous system,the NH gener- ates oxidation products NO,NO2 and HNO through different reaction paths,and the corresponding rate-determining step energy barriers are 120.67,323.37 and 193.50 kJ / mol,respectively. It was concluded that the process of the NO formation from ammonia-N / coal-N is easier to carry out. The kinetic results showed that the rate-determining step rate of NO formation is significantly higher than that of NO2 at all temperatures,and with the temperature increase,the rate-determining step rate of NO formation is gradually close to that of HNO. After the release of NH oxidation products,the residual oxygen on the char surface is further combined with C to form CO,which realizes the oxidation of N in ammonia fuel and C in pulverized coal in co-firing system. Then the char-N and O2 in the system undergoes a heterogeneous oxidation to realize the conversion of char-N to NO. This study revealed the molecular mechanism of the important transition product HNO formation in the process of ammonia combustion to NO at the microscopic lev- el,and clarified the formation path of another oxidation product NO2 ,which provides theoretical support and data refer- ence for the development of ammonia-coal co-combustion mechanism.

  • 关键词

    氨煤混烧NH煤焦-NNOHNO

  • KeyWords

    ammonia-coal co-firing;NH;char-N;NO;HNO

  • 引用格式
    陈萍,王莹,汪辉春,等.氨煤混燃过程中 NH/ 煤焦/ O2 异相体系 N 氧化的分子机理[J].煤炭学报,2023,48(2):1037-1046.
    CHEN Ping,WANG Ying,WANG Huichun,et al. Molecular mechanism of N oxidation in ammonia-coal co-firing [J].Journal of China Coal Society,2023,48(2):1037-1046.
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    • 煤焦-NH3和O2的优化结构

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