郭倩倩, 景文, 侯亚芹, 刘勇进, 李风海, 黄张根. HNO3改性促进活性炭低温脱硝机理的研究[J]. 燃料化学学报(中英文), 2021, 49(3): 387-394. DOI: 10.19906/j.cnki.JFCT.2021027
引用本文: 郭倩倩, 景文, 侯亚芹, 刘勇进, 李风海, 黄张根. HNO3改性促进活性炭低温脱硝机理的研究[J]. 燃料化学学报(中英文), 2021, 49(3): 387-394. DOI: 10.19906/j.cnki.JFCT.2021027
GUO Qian-qian, JING Wen, HOU Ya-qin, LIU Yong-jin, LI Feng-hai, HUANG Zhang-gen. Effects of HNO3 modification on the mechanism of low temperature NO reduction over activated carbon[J]. Journal of Fuel Chemistry and Technology, 2021, 49(3): 387-394. DOI: 10.19906/j.cnki.JFCT.2021027
Citation: GUO Qian-qian, JING Wen, HOU Ya-qin, LIU Yong-jin, LI Feng-hai, HUANG Zhang-gen. Effects of HNO3 modification on the mechanism of low temperature NO reduction over activated carbon[J]. Journal of Fuel Chemistry and Technology, 2021, 49(3): 387-394. DOI: 10.19906/j.cnki.JFCT.2021027

HNO3改性促进活性炭低温脱硝机理的研究

Effects of HNO3 modification on the mechanism of low temperature NO reduction over activated carbon

  • 摘要: 为了研究HNO3改性对活性炭(AC)低温脱硝机理的影响,采用HNO3在不同温度下对AC进行改性处理,改性前后样品在30−250 ℃进行脱硝活性测试,通过程序升温脱附(TPD)和瞬态响应实验对脱硝机理进行分析。结果表明,AC上NO转化率随反应温度升高逐渐降低再趋于稳定,反应物的吸附是速率控制步骤。含氧基团增加促进了NH3的吸附,但这部分吸附态NH3在30 ℃时几乎不参与反应,随反应温度升高不同程度活化,在30−90 ℃反应物的吸附是速率控制步骤,90 ℃后吸附态NH3的活化是速率控制步骤。

     

    Abstract: To study the effects of HNO3 modification on NO reduction over activated carbon (AC) at low temperatures, the AC was modified using HNO3 at different temperatures. The activity of the resulted activated carbons towards NO reduction with NH3 was investigated in a temperature range of 30−250 ℃. The temperature programmed desorption (TPD) and transient response experiments were used to study the mechanism of NO reduction. The results reveal that the NO conversion decreased with temperature at the initial stage and then kept stable. The adsorption of reactants was the rate-determining step. The increase of oxygen groups on the catalyst surface enhanced NH3 adsorption. The adsorbed NH3 hardly reacted with NO at 30 ℃. With increasing temperature, the adsorbed NH3 was gradually activated. In the temperature range of 30−90 ℃, the adsorption of reactants was rate-determining step of NO reduction. When the temperature was higher than 90 ℃, the reaction was dominated by the activation of adsorbed NH3.

     

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