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温度及盐酸浓度对改性SCR催化剂汞氧化能力的影响 被引量:2

Effect of temperature and hydrochloric acid concentration on mercury oxidation ability of modified SCR catalyst
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摘要 采用V、Ce活性溶液浸泡的方法对常规SCR催化剂进行改性,分析了HCl浓度、温度对其汞氧化能力的影响。结果表明,和常规催化剂相比,V改性催化剂样品中V2O5含量增大、比表面积和孔结构大幅下降,其汞氧化率低;Ce改性催化剂中新增活性物质CeO2、比表面积和孔结构略微减小,其汞氧化能力增强;各样品中的TiO2晶型均为锐钛型、活性物质分散均匀。烟气中含HCl时,催化剂氧化单质汞的机理类似Deacon途径,随着温度的升高,汞氧化率先增大后减小,最佳汞氧化温度为350℃;在温度200~400℃,HCl浓度0~60μL/L时,汞氧化率随着HCl浓度的增加而快速增加,在HCl浓度>60μL/L时趋于饱和。 The common SCR catalysts were quality changed by vanadium salt solution and cerium salt solution,and the effect of HCl concentration and temperature on the modified catalyst's mercury oxidation ability was investigated.The results showed that,compared with the general catalyst,the V2O5content in V modified catalyst increased,while the catalyst's specific surface area and pore structure decreased sharply,the mercury oxidation efficiency was lower;a new active matter CeO2appeared in the Ce modified catalyst,the catalyst's specific surface area and pore structure decreased a little,the mercury oxidation ability enhanced;the titanium dioxide in three samples were all anatase titanium dioxide and the active matters were uniformly distributed.The mercury oxidation mechanism was approximate as the Deacon process when HCl existed,and with an increase in temperature,the mercury oxidation efficiency first increased then decreased,the best mercury oxidation temperature were 350 ℃;within temperature range of 200to 400 ℃,the mercury oxidation efficiency increased rapidly with HCl concentration ranging from 0ppm to 60ppm,and tended to be saturated when HCl concentration was above 60ppm.
出处 《热力发电》 CAS 北大核心 2013年第7期60-64,69,共6页 Thermal Power Generation
关键词 SCR催化剂 钒、铈改性 汞氧化率 温度 盐酸 SCR catalyst vanadium cerium quality changed mercury oxidation efficiency temperature hydrochloric acid
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  • 1Pavlish J H,Sondreal E A,Mann M D. Status review of mercury control options for coal fired power plants[J].Fuel Processing Technology,2003,(2/3):89-91.
  • 2马英.典型燃煤电厂烟气汞协同控制研究[J].热力发电,2013,42(3):11-14. 被引量:6
  • 3赵毅,薛方明,董丽彦,邵媛.燃煤锅炉烟气脱汞技术研究进展[J].热力发电,2013,42(1):9-14. 被引量:26
  • 4孙巍,晏乃强,贾金平.负载硫氯化合物的活性炭去除单质汞的研究[J].环境科学与技术,2006,29(12):84-86. 被引量:17
  • 5高洪亮,周劲松,骆仲泱,岑可法.改性活性炭对模拟燃煤烟气中汞吸附的实验研究[J].中国电机工程学报,2007,27(8):26-30. 被引量:89
  • 6Hu C,Zhou J,He S. Effect of chemical activation of an activated carbon using zinc chloride on elemental mercury adsorption[J].Fuel Processing Technology,2009,(6):812-817.
  • 7EPRI. Electric utility traces substances synthesis report.EPRI TR-104614-V3,3(Appendix O)[R].1995.56-58.
  • 8Lee C W,Srivastava R K,Ghorishiet S B. Investigation of selective catalytic reduction impact on mercury speciation under simulated NOx emission control conditions[J].Journal of the Air And Waste Management Association,2004,(12):1560-1566.
  • 9Li H,Li Y,Wu C Y. Oxidation and capture of elemental mercury over SiO2-TiO2-V2O5 catalysts insimulated low-rank coal combustion flue gas[J].Chemical Engineering Journal,2011.186-193.
  • 10Li H,Wu C,LI Y. Superior activity of MnOxCeO2/TiO2 catalyst for catalytic oxidation of elemental mercury at low flue gas temperatures[J].Applied Catalysis B:Environmental,2012.381-388.

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