Effect of ZrO2 Crystal Structures on the Catalytic Performance of MnOx-CeO2/ZrO2 for Selective Reduction of NO with NH3 at Low Temperature

被引:2
作者
Xu, Yifan [1 ,2 ,3 ]
Liu, Rong [1 ,2 ,3 ]
Jia, Feng [4 ]
Ji, Lingchen [1 ,2 ,3 ]
Ye, Fei [5 ]
机构
[1] Nanjing Normal Univ, Sch Environm, Nanjing 025, Jiangsu, Peoples R China
[2] Nanjing Normal Univ, Jiangsu Ctr Collaborat Innovat Geog Informat Res, Nanjing 025, Jiangsu, Peoples R China
[3] Nanjing Normal Univ, Jiangsu Prov Key Lab Mat Cycling & Pollut Control, Nanjing 025, Jiangsu, Peoples R China
[4] Natl Chiao Tung Univ, Inst Environm Engn, Nanoparticle & Air Qual Lab, Shanghai 300, Peoples R China
[5] Minist Environm Protect, Nanjing Inst Environm Sci, Nanjing 025, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Selective Catalytic Reduction; Zirconia Polymorphs; Low Temperature; SO2; Poisoning; NITRIC-OXIDE; PART II; ZIRCONIA; MN; POLYMORPHS; PRECURSORS; MORPHOLOGY; FE-ZSM-5; PHASE; METAL;
D O I
10.1166/sam.2017.3124
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A series of manganese oxide and cerium oxide catalysts supported on monoclinic zirconia (m-ZrO2), tetragonal zirconia (t-ZrO2) and cubic zirconia (c-ZrO2) were prepared by a wet-impregnation method. The catalytic performance and SO2 tolerance for the selective reduction (SCR) of NOx with NH3 were investigated. Measurements were carried out in a fixed-bed reactor. The results suggested that both SCR activity (NO conversion on the catalysts) and SO2 tolerance of the prepared catalysts decreased in the following order: 5 wt.% MnOx-CeO2/c-ZrO2(5c) > 5 wt.% MnOx-CeO2/t-ZrO2(5t) > 5 wt.% MnOx-CeO2/m-ZrO2(5m) Surface properties are discussed by using XRD, BET, SEM, XPS, TPR, TPD and TG-DTA, FT-IR. 5 wt.% MnOx-CeO2/c-ZrO2 catalyst exhibited the best redox property and the highest adsorption capacity for NH3 while 5 wt.% MnOx-CeO2/m-ZrO2 and 5 wt.% MnOx-CeO2/t-ZrO2 catalysts exhibited relatively poor performance. Also, there existed the largest density of acid sites and highest strength of acidity when c-ZrO2 was used as carrier. The deterioration of active component and deposition of NH4HSO4, (NH4)(2)SO4 or metallic sulfites were identified as the main causes of SO2 poisoning.
引用
收藏
页码:2104 / 2113
页数:10
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