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Promoting effect of Ti addition on three-dimensionally ordered macroporous Mn-Ce catalysts for NH_3-SCR reaction: Enhanced N_2 selectivity and remarkable water resistance

机译:促进Ti加法对三维有序大孔Mn-Ce催化剂的NH_3-SCR反应的影响:增强N_2选择性和显着的耐水性

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摘要

A series of 3DOM-MnxCeyTiz catalysts with three-dimensionally ordered macroporous (3DOM) structure were synthesized by a soft template method. The high SCR activity of the 3DOM-Mn3Ce1 catalyst at low temperature was owing to the excellent redox ability and rich Lewis and Bronsted acid sites of the catalysts, which were beneficial to improve the catalytic activity. However, the strong oxidizability of MnOx resulted in the nonse-lective oxidation of NH3 and generation of N2O, decreasing the N-2 selectivity. After addition of Ti, the redox capacity of the 3DOM-Mn3Ce1Ti1 catalyst decreased, and the NH3 were strongly adsorbed on the acid sites, which enhanced the N-2 selectivity with a broadened temperature window of 240-440 degrees C and a high GHSV of 120000 h(-1). Furthermore, both the 3DOM-Mn3Ce1 and 3DOM-Mn3Ce1Ti1 catalysts showed remarkable tolerance of H2O. Finally, through in situ DRIFT analysis, the Langmuir-Hinshelwood (L-H) mechanism was confirmed as the dominant reaction pathway over the 3DOM-Mn3Ce1Ti1 catalyst.
机译:通过软模板法合成了具有三维有序大孔(3Dom)结构的一系列3Dom-Mnxceytiz催化剂。 3Dom-Mn3CE1催化剂在低温下的高疾病活性由于催化剂的优异氧化还原能力和富抗石油和铜烯烃位点,这有利于改善催化活性。然而,MNOX的强氧化性强调导致NH 3的非介绍氧化和N2O的产生,降低N-2选择性。在加入Ti之后,3Dom-Mn3CE1Ti1催化剂的氧化还原能力降低,NH 3牢固地吸附在酸部位上,该酸性位点增强了N-2选择性,增强了240-440℃的温度窗口和高GHSV 120000 h(-1)。此外,3Dom-Mn3CE1和3Dom-Mn3CE1Ti1催化剂显示出对H2O的显着耐受性。最后,通过原位漂移分析,证实了Langmuir-Hinshelwood(L-H)机理作为3Dom-Mn3CE1Ti1催化剂的显性反应途径。

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