Influence of preparation methods of supports on the deNO performance and alkali-metal resistance over TiO2/CeO2 catalysts in NH3-SCR reaction

催化作用 氧化还原 氮氧化物 材料科学 吸附 碱金属 色散(光学) 金属 分解 化学工程 热液循环 无机化学 化学 冶金 物理化学 燃烧 物理 有机化学 光学 工程类 生物化学
作者
Xin‐Kan Yao,Wanxia Zhao,Jian Rong,Wen Luo,Keke Kang,Lulu Long,Yang Chen
出处
期刊:Fuel [Elsevier BV]
卷期号:320: 123920-123920 被引量:12
标识
DOI:10.1016/j.fuel.2022.123920
摘要

Two kinds of CeO2 supports were synthesized by precipitation method and hydrothermal method, respectively, and then TiO2 species were loaded on their surface to prepare two TiO2/CeO2 catalysts (abbreviated as Ti/Ce-PM and Ti/Ce-HM). Experimental results show that Ti/Ce-PM and Ti/Ce-HM catalysts exhibit irregular nanoparticle morphology and specific tubular morphology, respectively, while the deNOx performance and anti-K poisoning ability of Ti/Ce-HM catalyst are worse than those of Ti/Ce-PM catalyst, which suggests that the random loading of TiO2 species on the tubular CeO2 support doesn’t enhance the deNOx performance and alkali-metal resistance. However, physicochemical property characterizations display that the excellent deNOx performance of Ti/Ce-PM catalyst can be attributed to better dispersion of TiO2 species, more excellent redox performance and surface acidity (especially B acid), larger Ce3+ content and Oα ratio, stronger electron interaction between Ce and Ti through the redox cycle of Ce3+ + Ti4+ ↔ Ce4+ + Ti3+, as well as easier desorption and decomposition of the adsorbed NOx species. Furthermore, stronger anti-K poisoning ability of Ti/Ce-PM catalyst results from that the negative impact of K2O species on the redox performance, surface acidity, Ce3+ content, and Oα ratio of Ti/Ce-PM catalyst is smaller than that on Ti/Ce-HM catalyst.
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