Porous washcoat structure in CeO2 modified Cu-SSZ-13 monolith catalyst for NH3-SCR with improved catalytic performance

被引:14
作者
Liu, Wuyuan [1 ]
Wang, Zhaoying [1 ]
Sun, Ming [1 ]
Gao, Jiajian [2 ]
Wang, Lifeng [3 ]
Gao, Zihan [1 ]
Xu, Yingying [1 ]
Zhao, Xiangyun [4 ]
Zhang, Cheng [5 ]
Yu, Lin [1 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Key Lab Clean Chem Technol Guangdong Regular High, Guangzhou 510006, Peoples R China
[2] ASTAR, Inst Sustainabil Chem Energy & Environm, Jurong Isl, Singapore
[3] Huizhou Ruihe Environm Technol Ltd, Huizhou, Peoples R China
[4] Shenzhen Candor Technol Ltd, Shenzhen, Peoples R China
[5] North Rare Earth Huakai High Tech Hebei Co Ltd, Hengshui, Peoples R China
关键词
low-temperature activity; mass transport; NH3-SCR; solvent combustion method; SSZ-13; zeolite; HYDROTHERMAL STABILITY; NO OXIDATION; REDUCTION; ZEOLITE; NH3; SCR; ENHANCEMENT; CU/SSZ-13; SITES; REDOX;
D O I
10.1002/aic.17834
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A series of CeO2 modified Cu-SSZ-13 monolith catalysts were prepared by embedding CeO2 into the washcoat of Cu-SSZ-13 monolith catalyst through solvent combustion method. These CexCu-SSZ-13 catalysts were studied in the selective catalytic reduction (SCR) of NO with NH3, among which the Ce2Cu-SSZ-13 catalyst exhibited the best low-temperature activity, hydrothermal stability, and sulfur resistance. The physicochemical properties of the catalysts were characterized using multiple methods. Results showed that the acidity, redox capacity, and ammonia adsorption capacity significantly enhanced after CeO2 modification, thus leading to the high performance of Ce2Cu-SSZ-13 catalyst. Furthermore, the introduction of CeO2 induced the fast SCR reaction by promoting the oxidation of NO to NO2. Analog calculation suggested that the porous structure generated via solvent combustion in the washcoat effectively increased the diffusion rate of reaction. In situ diffuse reflectance infrared Fourier transform spectroscopy (in situ DRIFT) analysis showed that Bronsted acid sites were the main active center and the reaction followed Eley-Rideal mechanism.
引用
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页数:13
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