环境化学

  • 罗晶,童志权,黄妍,夏斌,罗河.H2O和SO2对Cr-Ce/TiO2催化氧化NO性能的影响[J].环境科学学报,2010,30(5):1023-1029

  • H2O和SO2对Cr-Ce/TiO2催化氧化NO性能的影响
  • Effects of H2O and SO2 on a Cr-Ce/TiO2 catalyst for NO catalytic oxidation
  • 基金项目:湖南省自然科学基金资助项目(No.07JJ4003)
  • 作者
  • 单位
  • 罗晶
  • 湘潭大学环境科学与工程系, 湘潭 411105
  • 童志权
  • 湘潭大学环境科学与工程系, 湘潭 411105
  • 黄妍
  • 湘潭大学环境科学与工程系, 湘潭 411105
  • 夏斌
  • 湘潭大学环境科学与工程系, 湘潭 411105
  • 罗河
  • 湘潭大学环境科学与工程系, 湘潭 411105
  • 摘要:采用浸渍法在最佳制备条件下制备了新型Cr-Ce/TiO2催化剂,并对催化剂进行了BET和XRD表征.同时,考察了反应温度、H2O和SO2对该催化剂催化氧化NO性能的影响,并对中毒催化剂进行了FT-IR分析,讨论了中毒机理.结果表明,Cr-Ce/TiO2催化剂具有良好的NO氧化活性,在空速为10000h-1、O2体积分数8%(φ)、NO进口体积分数700×10-6条件下,反应温度250℃时NO转化率可达到59.7%,330℃时NO转化率可达到最大值80.7%.单独加入10%(φ)H2O或300×10-6(φ)SO2都可使催化剂活性降低,但在较高温度时影响较小.330℃下单独通入SO2和同时通入H2O与SO210h后,由于催化剂表面生成了少量硫酸盐和亚硫酸盐,活性下降并维持在62.4%左右,能够满足对NOx进行高效吸收的要求;停止通入H2O和SO2后,催化剂活性恢复到71.6%,加热处理后活性能进一步恢复到78.5%.该催化剂具有比文献中报道的其它NO氧化催化剂更强的抗H2O和SO2毒化能力.
  • Abstract:Chromium-cerium catalysts supported on TiO2 was prepared by impregnation under the optimum conditions and characterized by X-ray diffraction (XRD),and specific surface area measurement (BET). The effects of reaction temperature,H2Oand SO2 on catalytic oxidation of NO were investigated. The deactivation mechanisms in the presence of H2O and SO2 were analyzed by FT-IR. The results showed that Cr-Ce/TiO2 yielded a 59.7% NO conversion at 250 ℃,and 80.7% at 330 ℃ when the space velocity was 10000 h-1,O2 and NOconcentrations were 8% (φ) and 700×10-6 respectively. The activity of catalyst declined in the presence of only 10% (φ) H2O or 300×10-6 (φ) SO2 but this negative effect could be counteracted by increasing the reaction temperature. After reacting for 10 h in the presence of only SO2 or H2Oand SO2 together,a few sulfates and sulfites formed on the surface of the catalyst,and NOconversion was maintained at 62.4% which also satisfied the demands of highly efficient Absorption of NOx. The activity of the deactivated catalyst could recover to 71.6% after removing H2Oand SO2 and further recover to 78.5% after heat treatment. The catalyst showed substantial poison resistance for H2Oand SO2 compared with other reported catalysts for NOoxidation.

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