活性炭表面含氧官能团对燃煤烟气氮氧化物脱除的影响

许琦, 侯亚芹, 郭倩倩, 黄张根. 活性炭表面含氧官能团对燃煤烟气氮氧化物脱除的影响[J]. 环境化学, 2020, (8): 2105-2111. doi: 10.7524/j.issn.0254-6108.2019060505
引用本文: 许琦, 侯亚芹, 郭倩倩, 黄张根. 活性炭表面含氧官能团对燃煤烟气氮氧化物脱除的影响[J]. 环境化学, 2020, (8): 2105-2111. doi: 10.7524/j.issn.0254-6108.2019060505
XU Qi, HOU Yaqin, GUO Qianqian, HUANG Zhanggen. Effect of oxygen-containing functional groups on the removal of nitrogen oxides from coal-fired flue gas on activated carbon[J]. Environmental Chemistry, 2020, (8): 2105-2111. doi: 10.7524/j.issn.0254-6108.2019060505
Citation: XU Qi, HOU Yaqin, GUO Qianqian, HUANG Zhanggen. Effect of oxygen-containing functional groups on the removal of nitrogen oxides from coal-fired flue gas on activated carbon[J]. Environmental Chemistry, 2020, (8): 2105-2111. doi: 10.7524/j.issn.0254-6108.2019060505

活性炭表面含氧官能团对燃煤烟气氮氧化物脱除的影响

    通讯作者: 黄张根, E-mail: zghuang@sxicc.ac.cn
  • 基金项目:

    国家重点研发计划项目(2017YFC0210203)和山西省自然科学基金青年基金(201701D221058)资助.

Effect of oxygen-containing functional groups on the removal of nitrogen oxides from coal-fired flue gas on activated carbon

    Corresponding author: HUANG Zhanggen, zghuang@sxicc.ac.cn
  • Fund Project: Supported by the National Key Research and Development Program (2017YFC0210203) and the Shanxi Province Science Foundation (201701D221058).
  • 摘要: 采用HNO3、H2SO4及H2O2对煤基活性炭进行氧化改性处理,研究低温(<250℃)下NH3为还原剂的选择催化还原(SCR)NOx的反应性能.通过元素分析、表面积和孔分布、Boehm滴定、TPD-MS、XPS分析对氧化前后活性炭表面物理化学性质进行分析,对表面含氧基团含量进行了定性定量研究.结果表明,与H2SO4及H2O2处理后相比,活性炭经HNO3氧化处理后表面羧基、酸酐和羟基含量明显增加,在考察温度范围内SCR活性明显提高,HNO3是最佳氧化剂.含氧基团含量与SCR活性的关联结果表明,羧基、酸酐和羟基等3种含氧基团对HNO3改性后活性炭样品的SCR活性提高发挥主要作用.
  • 加载中
  • [1] 赵永椿,马斯鸣,杨建平,等. 燃煤电厂污染物超净排放的发展及现状[J].煤炭转化, 2015, 40(11):2629-2640.

    ZHAO Y C, MA S M, YANG J P, et al. Development and current status of ultra-clean emissions of pollutants from coal-fired power plants[J].Coal Conversion, 2015, 40(11):2629-2640(in Chinese).

    [2] 晋华东,景文,黄张根,等. 两种钒炭催化剂低温选择性催化还原脱硝性能比较及分析[J].环境化学, 2013, 32(10):1869-1873.

    JIN H D, JING W, HUANG Z G, et al, Comparison and analysisof the performance of two vanadium loaded carbon-based catalysts for the low temperature SCR of NO by ammonia[J].Environmental Chemistry, 2013, 32(10):1869-1873(in Chinese).

    [3] 李雪飞,张文辉,杜铭华. 干法烟气脱硝综述[J].洁净煤技术, 2006, 12(3):43-46.

    LI X F, ZHANG W H, DU M H, Summary of dry flue gas denitrification[J]. Clean Coal Technology, 2006, 12(3):43-46(in Chinese).

    [4] 郭旸旸,李玉然,朱廷钰,等.活性炭吸附法同时脱硫脱硝[C]//第七届全国环境化学大会摘要集,2013. GUO Y Y, LI Y R, ZHU T Y, et al, Simultaneous desulfurization and denitrification by activated carbon adsorption[C]//Summary of the 7th National Conference on Environmental Chemistry,2013(in Chinese).
    [5] TSUJI K,SHIRAISHI I. Combined desulfurization,denitrification and reduction of air toxics using activated coke:Activity of activated coke[J]. Fuel,1997,76(6):549-553.
    [6] 赵德生.太钢450 m2烧结机烟气脱硫脱硝工艺实践[C]//全国烧结烟气脱硫技术交流会论文集, 2011, 8-15. ZHAO D S, Practice of flue gas desulfurization and denitrification process for 450 m2

    sintering gas of Taiyuan Iron and Steel Co[C]//Proceedings of National Sintering Flue Gas Desulfurization Technology, 2011, 8-15(in Chinese).

    [7] GARCIA -BORDEJE E, LAZARO M J, MOLINER R, et al. Vanadium supported on carbon coated honeycomb monoliths for the selective catalytic reduction of NO at low temperatures:Influence of the oxidation pre-treatment[J]. Carbon, 2006, 44(3):407-417.
    [8] BOYANO A, HERRERA C, LARRUBIA M A, et al. Vanadium loaded carbon-based monoliths for the on-board no reduction:Influence of temperature and period of the oxidation treatment[J]. Chemical Engineering Journal, 2010, 160(2):623-633.
    [9] TENG H, TU Y T, LAI Y C, et al. Reduction of NO with NH3 over carbon catalysts:The effects of treating carbon with H2SO4 and HNO3[J]. Carbon, 2001, 39(4):575-582.
    [10] ZHU L, HUANG B, WANG W, et al. Low-temperature SCR of NO with NH3 over CeO2 supported on modified activated carbon fibers[J]. Catalysis Communications, 2011, 12(6):394-398.
    [11] BOYANO A, GALVEZ M E, MOLINER R, et al. Carbon-based catalytic briquettes for the reduction of NO:Effect of H2SO4 and HNO3 carbon support treatment[J]. Fuel, 2008, 87(10/11):2058-2068.
    [12] GALVEZ M E, LAZARO M J, MOLINER R. Novel activated carbon-based catalyst for the selective catalytic reduction of nitrogen oxide[J]. Catalysis Today, 2005, 102-103:142-147.
    [13] HUANG M C, TENG H. Nitrogen-containing carbons from phenol-formaldehyde resins and their catalytic activity in NO reduction with NH3[J]. Carbon, 2003, 41(5):951-957.
    [14] AHMED S N, BALDWIN R, DERBYSHIRE F, et al. Catalytic reduction of nitric oxide over activated carbons[J]. Fuel, 1993, 72(3):287-292.
    [15] ZHU Z, LIU Z, LIU S, et al. NO reduction with NH3 over an activated carbon-supported copper oxide catalysts at low temperatures[J]. Applied Catalysis B:Environmental, 2000, 26(1):25-35.
    [16] SZYMANSKI G S, KARPINSKI Z, BINIAK S, et al. The effect of the gradual thermal decomposition of surface oxygen species on the chemical and catalytic properties of oxidized activated carbon[J]. Carbon, 2002, 40(14):2627-2639.
    [17] FIGUEIREDO J L, PERAIRA M F R, FREITAS M A, et al. Modification of the surface chemistry of activated carbons[J]. Carbon, 1999, 37(9):1379-1389.
    [18] 佟莉,徐文青,元昊, 等. 硝酸改性活性炭上氧/氮官能团对脱汞性能的促进作用[J].物理化学学报, 2015,31(3):512-518.

    TONG L, XU W Q, YUAN H, et al, Enhanced Effect of O/N groups on the Hg0 removal efficiency over the HNO3-modified activated carbon[J]. Acta Phys.-Chim. Sin, 2015,31(3):512-518(in Chinese).

    [19] MORALES-TORRES S, SILVA T L S, PASTRANA-MARTINEZ L M, et al. Modification of the surface chemistry of singleand multi-walled carbon nanotubes by HNO3 and H2SO4 hydrothermal oxidation for application in direct contact membrane distillation[J]. Physical Chemistry Chemical Physics, 2014, 16(24):12237-12250.
    [20] ZHOU J H, SUI Z J, ZHU J, et al. Characterization of surface oxygen complexes on carbon nanofibers by TPD, XPS and FT-IR[J]. Carbon, 2007, 45(4):785-796.
    [21] SWIATKOWSKIi A, PAKULA M, BINIAK S, et al. Influence of the surface chemistry of modified activated carbon on its electrochemical behaviour in the presence of lead(Ⅱ) ions[J]. Carbon, 2004, 42(15):3057-3069.
  • 加载中
计量
  • 文章访问数:  2302
  • HTML全文浏览数:  2302
  • PDF下载数:  52
  • 施引文献:  0
出版历程
  • 收稿日期:  2019-06-05

活性炭表面含氧官能团对燃煤烟气氮氧化物脱除的影响

    通讯作者: 黄张根, E-mail: zghuang@sxicc.ac.cn
  • 1. 国电电力发展股份有限公司, 北京, 100101;
  • 2. 中国科学院山西煤炭化学研究所, 煤转化国家重点实验室, 太原, 030001
基金项目:

国家重点研发计划项目(2017YFC0210203)和山西省自然科学基金青年基金(201701D221058)资助.

摘要: 采用HNO3、H2SO4及H2O2对煤基活性炭进行氧化改性处理,研究低温(<250℃)下NH3为还原剂的选择催化还原(SCR)NOx的反应性能.通过元素分析、表面积和孔分布、Boehm滴定、TPD-MS、XPS分析对氧化前后活性炭表面物理化学性质进行分析,对表面含氧基团含量进行了定性定量研究.结果表明,与H2SO4及H2O2处理后相比,活性炭经HNO3氧化处理后表面羧基、酸酐和羟基含量明显增加,在考察温度范围内SCR活性明显提高,HNO3是最佳氧化剂.含氧基团含量与SCR活性的关联结果表明,羧基、酸酐和羟基等3种含氧基团对HNO3改性后活性炭样品的SCR活性提高发挥主要作用.

English Abstract

参考文献 (21)

目录

/

返回文章
返回