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Environ Sci Technol


Title:Rationally Engineering a CuO/Pd@SiO(2) Core-Shell Catalyst with Isolated Bifunctional Pd and Cu Active Sites for n-Butylamine Controllable Decomposition
Author(s):Ma M; Xu S; Liu Q; Xu J; Li Y; Sun Y; Yu Y; Chen C; Chen Z; Li L; Zheng C; He C;
Address:"State Key Laboratory of Multiphase Flow in Power Engineering, School of Energy and Power Engineering, Xi'an Jiaotong University, Xi'an710049, Shaanxi, P.R. China. School of Chemical and Biomedical Engineering, Nanyang Technological University, 637459Singapore. Key Laboratory of Subsurface Hydrology and Ecological Effects in Arid Region, Ministry of Education, School of Water and Environment, Chang'an University, Xi'an710064, P.R. China. National Engineering Laboratory for VOCs Pollution Control Material and Technology, University of Chinese Academy of Sciences, Beijing101408, P.R. China"
Journal Title:Environ Sci Technol
Year:2022
Volume:20221010
Issue:22
Page Number:16189 - 16199
DOI: 10.1021/acs.est.2c04256
ISSN/ISBN:1520-5851 (Electronic) 0013-936X (Linking)
Abstract:"Volatile organic amines are a category of typical volatile organic compounds (VOCs) extensively presented in industrial exhausts causing serious harm to the atmospheric environment and human health. Monometallic Pd and Cu-based catalysts are commonly adopted for catalytic destruction of hazardous organic amines, but their applications are greatly limited by the inevitable production of toxic amide and NO(x) byproducts and inferior low-temperature activity. Here, a CuO/Pd@SiO(2) core-shell-structured catalyst with diverse functionalized active sites was creatively developed, which realized the total decomposition of n-butylamine at 260 degrees C with a CO(2) yield and N(2) selectivity reaching up to 100% and 98.3%, respectively (obviously better than those of Pd@SiO(2) and CuO/SiO(2)), owing to the synergy of isolated Pd and Cu sites in independent mineralization of n-butylamine and generation of N(2), respectively. The formation of amide and short-chain aliphatic hydrocarbon intermediates via C-C bond cleavage tended to occur over Pd sites, while the C-N bond was prone to breakage over Cu sites, generating NH(2). species and long free-N chain intermediates at low temperatures, avoiding the production of hazardous amide and NO(x). The SiO(2) channel collapse and H(+) site production resulted in the formation of N(2)O via suppressing NH(2). diffusion. This work provides critical guidance for a rational fabrication of catalysts with high activity and N(2) selectivity for environmentally friendly destruction of nitrogen-containing VOCs"
Keywords:Humans *Silicon Dioxide/chemistry Catalytic Domain *Butylamines Amides CuO/Pd@SiO2 core-shell catalytic destruction isolated active sites n-butylamine reaction mechanism;
Notes:"MedlineMa, Mudi Xu, Shuai Liu, Qiyuan Xu, Junwei Li, Yuliang Sun, Yukun Yu, Yanke Chen, Changwei Chen, Zhaohui Li, Lu Zheng, Chunli He, Chi eng Research Support, Non-U.S. Gov't 2022/10/11 Environ Sci Technol. 2022 Nov 15; 56(22):16189-16199. doi: 10.1021/acs.est.2c04256. Epub 2022 Oct 10"

 
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