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共沉淀法和浸渍法制备的HoCeMn/TiO2催化剂的脱硝性能

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采用浸渍法和共沉淀法制备了 HoCeMn/TiO2脱硝催化剂并对其结构和性能进行了表征.结果表明共沉淀法增强了活性组分和载体的相互作用,从而增加了 HoCeMnTi-C催化剂表面Ce3+、Mn4+以及吸附氧的含量,使其表现出优异的低温氧化还原性能.此外,共沉淀法制备的HoCeMnTi-C具有更多的表面酸性位点及更强的表面酸性.催化剂表面酸性和氧化还原性能的提高有助于氨的吸附和活化,从而显著提高其活性.表面酸性位点的增多还抑制了H2O和SO2在催化剂表面的吸附,提升了催化剂的抗水抗硫性能.催化剂上的选择性催化还原(SCR)反应遵循Eley-Rideal(E-R)机制,催化剂硫中毒是源于形成的硫酸盐覆盖或破坏了催化剂活性位.
Denitration performance of HoCeMn/TiO2 catalysts prepared by co-precipitation and impregnation methods
Impregnation and co-precipitation methods were used to synthesize HoCeMn/TiO2 catalysts for the reduc-tion of NOx with NH3.Different kinds of characterization methods were used to explore the structures and perfor-mances of the catalysts.The results show that the co-precipitation method enhances the interactivity between the active component and carrier,thereby increasing the content of Ce3+,Mn4+,and adsorption oxygen on the surface of HoCeMnTi-C.As a result,it showed excellent low-temperature redox performance.In addition,HoCeMnTi-C pre-pared by the co-precipitation method possessed more surface acidic sites and stronger surface acidity.The improve-ment of surface acidity and redox performance is conducive to the adsorption and activation of ammonia,and there-by significantly improved its activity.The increase of acidic sites also restrained the adsorption of H2O and SO2,and therefore sulfur and water resistance of HoCeMnTi-C were significantly promoted.The reaction of selective catalytic reduction(SCR)on catalysts obeys the Eley-Rideal(E-R)mechanism.SO2 poisoning of catalysts was caused by the formation of sulfates,which cover or damage the active sites of the catalysts.

HoCeMn/TiO2 catalystactivitywater and sulfur resistance

黄利华、华坚

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西南科技大学环境与资源学院,绵阳 621010

国家烟气脱硫工程技术中心,成都 610065

HoCeMn/TiO2催化剂 活性 抗水抗硫性能

2024

无机化学学报
中国化学会

无机化学学报

CSTPCD北大核心
影响因子:0.665
ISSN:1001-4861
年,卷(期):2024.40(3)
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