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Sulfur resistance of Ce-Mn/TiO2 catalysts for low-temperature NH3–SCR

机译:Ce-Mn / TiO2催化剂对低温NH3-SCR的抗硫性

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摘要

Ce-Mn/TiO2 catalyst prepared using a simple impregnation method demonstrated a better low-temperature selective catalytic reduction of NO with NH3 (NH3–SCR) activity in comparison with the sol-gel method. The Ce-Mn/TiO2 catalyst loading with 20% Ce had the best low-temperature activity and achieved a NO conversion rate higher than 90% at 140–260°C with a 99.7% NO conversion rate at 180°C. The Ce-Mn/TiO2 catalyst only had a 6% NO conversion rate decrease after 100 ppm of SO2 was added to the stream. When SO2 was removed from the stream, the catalyst was able to recover completely. The crystal structure, morphology, textural properties and valence state of the metals involving the novel catalysts were investigated using X-ray diffraction, N2 adsorption and desorption analysis, X-ray photoelectron spectroscopy, scanning electron microscopy and energy dispersive spectroscopy, respectively. The decrease of NH3–SCR performance in the presence of 100 ppm SO2 was due to the decrease of the surface area, change of the pore structure, the decrease of Ce4+ and Mn4+ concentration and the formation of the sulfur phase chemicals which blocked the active sites and changed the valence status of the elements.
机译:与溶胶-凝胶法相比,使用简单的浸渍方法制备的Ce-Mn / TiO2催化剂表现出更好的低温选择性催化还原NH3(NH3-SCR)活性。 Ce含量为20%的Ce-Mn / TiO2催化剂具有最佳的低温活性,在140–260°C时NO转化率高于90%,在180°C时NO转化率为99.7%。在将100 streamppm的SO2添加到物流中之后,Ce-Mn / TiO2催化剂的NO转化率仅降低了6%。当从物流中除去SO 2时,催化剂能够完全回收。分别使用X射线衍射,N2吸附和解吸分析,X射线光电子能谱,扫描电子显微镜和能谱仪研究了涉及新型催化剂的金属的晶体结构,形态,结构性质和化合价态。在100 ppm SO2存在下,NH3-SCR性能的下降是由于表面积的减少,孔结构的变化,Ce 4 + 和Mn 4+的下降浓度和硫相化学物质的形成阻止了活性位点并改变了元素的价态。

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