共 53 条
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
论文数: 0 引用数: 0
h-index: 0
机构:
Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China

Zhang, Shule
论文数: 0 引用数: 0
h-index: 0
机构:
Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China

Zhang, Mingjia
论文数: 0 引用数: 0
h-index: 0
机构:
Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China

Zhong, Qin
论文数: 0 引用数: 0
h-index: 0
机构:
Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China
机构:
[1] Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China
来源:
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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