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Oxidation of elemental mercury by modified spent TiO2-based SCR-DeNO(x) catalysts in simulated coal-fired flue gas

机译:改性的基于TiO2的废SCR-DeNO(x)催化剂在模拟燃煤烟气中氧化元素汞

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In order to reduce the costs, the recycle of spent TiO2-based SCR-DeNO(x) catalysts were employed as a potential catalytic support material for elemental mercury (Hg-0) oxidation in simulated coal-fired flue gas. The catalytic mechanism for simultaneous removal of Hg-0 and NO was also investigated. The catalysts were characterized by Brunauer-Emmett-Teller (BET), scanning electron microscope (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) method. Results indicated that spent TiO2-based SCR-DeNO(x) catalyst supported Ce-Mn mixed oxides catalyst (CeMn/SCR1) was highly active for Hg-0 oxidation at low temperatures. The Ce1.00Mn/SCR1 performed the best catalytic activities, and approximately 92.80 % mercury oxidation efficiency was obtained at 150 A degrees C. The inhibition effect of NH3 on Hg-0 oxidation was confirmed in that NH3 consumed the surface oxygen. Moreover, H2O inhibited Hg-0 oxidation while SO2 had a promotional effect with the aid of O-2. The XPS results illustrated that the surface oxygen was responsible for Hg-0 oxidation and NO conversion. Besides, the Hg-0 oxidation and NO conversion were thought to be aided by synergistic effect between the manganese and cerium oxides.
机译:为了降低成本,废TiO2基SCR-DeNO(x)催化剂的循环被用作模拟燃煤烟气中元素汞(Hg-0)氧化的潜在催化载体材料。还研究了同时去除Hg-0和NO的催化机理。通过Brunauer-Emmett-Teller(BET),扫描电子显微镜(SEM),X射线衍射(XRD)和X射线光电子能谱(XPS)方法对催化剂进行了表征。结果表明,废TiO2基SCR-DeNO(x)催化剂负载的Ce-Mn混合氧化物催化剂(CeMn / SCR1)在低温下对Hg-0氧化具有很高的活性。 Ce1.00Mn / SCR1表现出最佳的催化活性,在150 A的温度下可获得约92.80%的汞氧化效率。NH3消耗了表面氧,证实了NH3对Hg-0氧化的抑制作用。此外,H2O抑制了Hg-0的氧化,而SO2在O-2的帮助下具有促进作用。 XPS结果表明表面氧是Hg-0氧化和NO转化的原因。此外,Hg-0的氧化和NO的转化被认为是由锰和铈的氧化物之间的协同作用所辅助的。

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