Efficient catalytic ozonation of ethyl acetate over Cu-Mn catalysts: Further insights into the reaction mechanism

被引:2
|
作者
Sun, Yulin [1 ]
Liu, Peixi [1 ]
Wang, Zhihua [1 ]
Tang, Hairong [2 ]
He, Yong [1 ]
Zhu, Yanqun [1 ]
机构
[1] Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Peoples R China
[2] Nucl Power Inst China, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Redox-precipitation method; Ethyl acetate; Catalytic ozonation; Cu-Mn oxides; Reaction mechanism; IN-SITU FTIR; MANGANESE OXIDES; COMPOSITE OXIDES; GASEOUS OZONE; OXIDATION; TOLUENE; PERFORMANCE; REMOVAL; BENZENE; PHASE;
D O I
10.1016/j.cej.2023.147282
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A series of Cu-Mn oxides were synthesized by the redox-precipitation method with different precipitants to evaluate the catalytic ozonation of ethyl acetate (EA). It was found that CuMn-II (with H2C2O4 as precipitant) exhibited the best catalytic activity, which achieved an EA conversion of 99 % at 120 degrees C with an O3/EA molar ratio of 10. The reaction temperature, O3/EA molar ratio, ozone utilization rate, and COx selectivity were also discussed. Meanwhile, many characterizations were conducted to reveal the properties of catalysts, such as SEM, XRD, BET, XPS, H2-TPR and NH3-TPD. Abundant surface defects, plentiful oxygen vacancies, larger specific surface area, higher content of Mn3+ and more acid sites contributed to the superior performance of CuMn-II. Catalyst poisoning occurred when SO2 was added, however, the conversion of EA could gradually recover to 88 % once SO2 was stopped. In-situ DRIFTS measurement was carried out to reveal the formation of intermediate species during the reaction. Combined with DFT calculations, a reaction mechanism for the catalytic ozonation of EA over CuMn2O4 catalysts was proposed.
引用
收藏
页数:11
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