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« Previous AbstractA combined evaluation of the characteristics and acute toxicity of antibiotic wastewater    Next Abstract"Enhanced Water Resistance and Catalytic Performance of Ru/TiO(2) by Regulating Bronsted Acid and Oxygen Vacancy for the Oxidative Removal of 1,2-Dichloroethane and Toluene" »

Environ Sci Technol


Title:"High Selectivity to HCl for the Catalytic Removal of 1,2-Dichloroethane Over RuP/3DOM WO(x): Insights into the Effects of P-Doping and H(2)O Introduction"
Author(s):Yu X; Dai L; Peng Y; Deng J; Liu Y; Jing L; Zhang X; Hou Z; Wang J; Dai H;
Address:"Beijing Key Laboratory for Green Catalysis and Separation, Key Laboratory of Beijing on Regional Air Pollution Control, Key Laboratory of Advanced Functional Materials, Education Ministry of China, Laboratory of Catalysis Chemistry and Nanoscience, Department of Environmental Chemical Engineering, School of Environmental and Chemical Engineering, Faculty of Environment and Life, Beijing University of Technology, Beijing 100124, P. R. China. John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States. State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, P. R. China"
Journal Title:Environ Sci Technol
Year:2021
Volume:20211011
Issue:21
Page Number:14906 - 14916
DOI: 10.1021/acs.est.1c05586
ISSN/ISBN:1520-5851 (Electronic) 0013-936X (Linking)
Abstract:"Ru-based catalysts for catalytic combustion of high-toxicity Cl-containing volatile organic compounds are inclined to produce Cl(2) instead of ideal HCl due to the Deacon reaction. We herein reported that the three-dimensionally ordered macroporous (3DOM) WO(x)-supported RuP nanocatalyst greatly improved HCl selectivity (at 400 degrees C, increased from 66.0% over Ru/3DOM WO(x) to 96.4% over RuP/3DOM WO(x)) and reduced chlorine-containing byproducts for 1,2-dichloroethane (1,2-DCE) oxidation. P-doping enhanced the number of structural hydroxyl groups and Bronsted acid sites. The isotopic 1,2-DCE temperature-programmed desorption experiment in the presence of H(2)(18)O indicated the generation of a new active oxygen species (16)O(18)O that participated in the reaction. Generally, P-doping and H(2)O introduction could promote the exchange reaction between Cl and hydroxyl groups, rather than oxygen defects, and then benefit the production of HCl and reduce the generation of other chlorine species or Cl(2), via the reaction processes of C(2)H(3)Cl --> alcohol --> aldehyde --> carboxylic acids"
Keywords:"Catalysis *Ethylene Dichlorides Oxidation-Reduction Reactive Oxygen Species 1, 2-dichloroethane oxidation HCl selectivity macroporous tungsten oxide supported ruthenium catalyst phosphorus doping water resistance;"
Notes:"MedlineYu, Xiaohui Dai, Lingyun Peng, Yue Deng, Jiguang Liu, Yuxi Jing, Lin Zhang, Xing Hou, Zhiquan Wang, Jia Dai, Hongxing eng Research Support, Non-U.S. Gov't 2021/10/12 Environ Sci Technol. 2021 Nov 2; 55(21):14906-14916. doi: 10.1021/acs.est.1c05586. Epub 2021 Oct 11"

 
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