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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.
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页数:11
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