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Study on the Kinetics of NO Removal from Simulated Flue Gas by a Wet Ultraviolet/H_2O_2 Advanced Oxidation Process

机译:湿法紫外/ H_2O_2高级氧化工艺去除模拟烟气中NO的动力学研究

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摘要

On the basis of the steady-state approximation theory and the two-film theory, the kinetic model of NO removal by a wet ultraviolet (UV)/H_2O_2 advanced oxidation process (AOP) was established. The mass-transfer reaction kinetic process of NO removal was also analyzed preliminarily. The results showed that the NO removal process by the wet UV/H_2O_2 AOP was a pseudo-first-order reaction for NO. The NO absorption process in the wet UV/H_2O_2 AOP system belonged to the fast reaction kinetic region. The chemical reaction process could be completed in the liquid film. The NO absorption rate mainly depended upon the chemical reaction rate, the diffusion rate, and the NO partial pressure, but it was not affected by the liquid-phase mass-transfer coefficient. Therefore, the NO absorption rate could be increased by improving the chemical reaction conditions, increasing the gas-liquid contact area, and raising the NO partial pressure. The comparison of experimental values and model values of pseudo-first-order reaction rate constants showed that the mass-transfer reaction kinetic model deduced had good reliability.
机译:基于稳态近似理论和两层膜理论,建立了湿紫外(H)/ H_2O_2高级氧化工艺(AOP)去除NO的动力学模型。初步分析了脱氮的传质反应动力学过程。结果表明,湿式UV / H_2O_2 AOP去除NO的过程是NO的拟一级反应。湿法UV / H_2O_2 AOP体系中的NO吸收过程属于快速反应动力学区域。化学反应过程可以在液膜中完成。 NO吸收速率主要取决于化学反应速率,扩散速率和NO分压,但不受液相传质系数的影响。因此,可以通过改善化学反应条件,增加气液接触面积以及提高NO分压来提高NO吸收率。实验值与拟一级反应速率常数的模型值的比较表明,推导的传质反应动力学模型具有良好的可靠性。

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  • 来源
    《Energy & fuels》 |2011年第maraaapra期|p.1547-1552|共6页
  • 作者单位

    School of Energy and Environment, Southeast University, Nanjing 210096, People's Republic of China;

    School of Energy and Environment, Southeast University, Nanjing 210096, People's Republic of China;

    School of Energy and Environment, Southeast University, Nanjing 210096, People's Republic of China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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