OH自由基对NH3选择性非催化还原NO作用机制的密度泛函理论计算研究

DFT study on role of OH radical in selective non-catalytic reduction of NO by NH3

  • 摘要: 氮氧化物(NOx)是燃煤电厂产生的主要污染物之一,选择性非催化还原(Selective Non-Catalytic Reduction, SNCR)脱硝技术由于结构简单、成本低且不需要使用催化剂等优点,得到广泛的应用。SNCR脱硝过程会产生大量OH自由基,深入探究SNCR过程中OH自由基的作用机制对提高SNCR脱硝效率很有必要。基于密度泛函理论(Density Functional Theory,DFT)探究了OH自由基对NH3选择性非催化还原NO的作用机制。结果表明:NH3+NO反应存在3条反应路径,最优反应路径为NH3和NO首先反应生成中间体NH2NO和一个孤立的H原子,孤立的H原子攻击NH2NO中的O原子,形成NH2N和OH,继而生成NNH和H2O,其中NH3脱除第1个氢原子的过程需要克服的能垒(265.0 kJ/mol)最高,是整个反应的决速步骤。NH2+NO反应的决速步能垒(140.2 kJ/mol)较NH3+NO反应(265.0 kJ/mol)低124.8 kJ/mol,表明NH2+NO脱硝反应速率更快。NH3+NO+OH反应决速步能垒(198.7 kJ/mol)较NH3+NO反应(265.0 kJ/mol)降低了66.3 kJ/mol,OH自由基主要是通过促进NH3脱除第1个氢原子产生NH2来提高NH3+NO脱硝反应效率。NH3+NO+OH反应机理与NH2+NO反应机理基本一致。OH自由基参与NH2+NO脱硝反应可以形成六元络合物结构,促进脱硝反应进行。OH自由基不仅可以显著提高NH3+NO脱硝反应速率,也能够促进较低温度(673~1 273 K)下NH2+NO脱硝反应速率。OH自由基可以降低NH3+NO以及NH2+NO反应的活化能,促进脱硝反应。对于NH3选择性非催化还原NO过程,NH3脱除第1个氢原子生成NH2是决速步骤,加快该过程是提高SNCR脱硝效率的关键。

     

    Abstract: Nitrogen oxides (NOx) is one of the main pollutants produced by coal-fired power plants. Selective non-catalytic reduction (SNCR) denitration technology has been widely used due to its advantages of simple structure, low cost and no need for catalyst. A large number of OH radicals are produced in the process of SNCR denitration. It is necessary to explore the role of OH radical to improve the efficiency of SNCR denitration. Based on density functional theory (DFT), the role of OH radical in the selective non-catalytic reduction of NO by NH3 was explored. The results showed that there are three reaction pathways for the reaction of NH3 and NO, and the optimal reaction pathway is that NH3 and NO first react to form the intermediate NH2NO and an isolated H atom, which attacks the O atom of NH2NO to form OH and NH2N, followed by the formation of NNH and H2O. The process of removing the first hydrogen atom from NH3 requires the highest energy barrier (265.0 kJ/mol), which is the rate-limiting step. The energy barrier of rate-limiting step of NH2+NO reaction (140.2 kJ/mol) is 124.8 kJ/mol lower than that of NH3+NO reaction (265.0 kJ/mol), indicating that the denitration reaction rate of NH2+NO is faster. The energy barrier of rate-limiting step of NH3+NO+OH reaction (198.7 kJ/mol) is 66.3 kJ/mol lower than that of NH3+NO reaction (265.0 kJ/mol). The OH radical improves the denitration efficiency of NH3+NO mainly by promoting the removal of the first hydrogen atom from NH3 to produce NH2. The reaction mechanism of NH3+NO+OH is similar to that of NH2+NO. The OH radical participating in NH2+NO denitration reaction can form a six-element complex structure and promote denitration reaction. The OH radical can not only significantly improve the denitration reaction rate of NH3+NO, but also promote the denitration reaction rate of NH2+NO at a lower temperature (673−1 273 K). The OH radical can reduce the activation energy of NH3+NO and NH2+NO reactions, promoting the denitration reaction. For the selective non-catalytic reduction of NO with NH3, the removal of the first hydrogen atom from NH3 to NH2 is the rate-limiting step, and accelerating this process is the key to improve the denitration efficiency of SNCR.

     

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