TiO2 with exposed {001} facets catalyzed peroxone reaction into •O2- and •OH radicals for low temperature NO oxidation

被引:4
作者
Meng, Fanyu [1 ]
Zhang, Shule [1 ]
Zhang, Mingjia [1 ]
Zhong, Qin [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; {001} facets; O-3/H2O2; NO oxidation; Promotional mechanism; FLUE-GAS; PHOTOCATALYTIC ACTIVITY; RAMAN-SPECTROSCOPY; SINGLE-CRYSTALS; REMOVAL; SO2; REDUCTION; OZONE; PERCENTAGE; MECHANISM;
D O I
10.1016/j.fuel.2021.122748
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The peroxone reaction (O-3/H2O2) on the surface of TiO2 to generate center dot O-2(-) and center dot OH is an efficient method for pollutant control. In the present work, anatase TiO2 with a high percentage of exposed {001} facets were synthesized and investigated in O-3/H2O2 process, which exhibited an excellent performance for NO oxidation. Experimental results showed that NO oxidation efficiency reached 98 % at the molar ratio of H2O2/NO = 4.36 and O-3/NO = 0.5. The promotion mechanism for NO oxidation was proposed: TiO2 with exposed {001} facets could improve the adsorption of O-3, and enhance the activation of H2O2. A significant synergistic effect between O-3 and H2O2 over TiO2(001) catalyst inducing center dot OH and center dot O-2(-) radicals, which was contributed to NO oxidation. Furthermore, the reaction mechanism of the O-3/H2O2/TiO2(001) process was further revealed by in-situ DRIFTS, and the main product was NO3-. Moreover, O-3/H2O2/TiO2(001) exhibited the stable NO oxidation performance under different gas component including CO, CO2 and SO2.
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页数:10
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