The Catalytic and Adsorptive Synergistic Effect of Oxygen-Vacancy-Rich MnO x /C Catalysts for HCHO Oxidation at Room Temperature

被引:0
|
作者
Li, Mengmeng [1 ]
Xu, Hao [1 ]
Hou, Yuanming [1 ]
Fu, Xianwei [1 ]
Yang, Jianjun [1 ]
Li, Qiuye [1 ]
机构
[1] Henan Univ, Engn Res Ctr Nanomat, Natl & Local Joint Engn Res Ctr Appl Technol Hybri, Kaifeng 475004, Henan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
BIRNESSITE-TYPE MNO2; FORMALDEHYDE OXIDATION; MANGANESE OXIDES; CARBON; REMOVAL; SPECTRA; NANOSTRUCTURES; DELTA-MNO2;
D O I
10.1021/acs.iecr.3c04304
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Indoor formaldehyde (HCHO) pollution has attracted extensive attention and shows a carcinogenic effect on humans. However, removal of HCHO still faces the issues of low activity and high-loading noble metals. Herein, we combined catalysis and adsorption into the MnOx /C composite catalysts with abundant oxygen vacancy (V-O), which were prepared through a facile in situ synthesis approach between fructose and KMnO4. With the addition of fructose during preparation, the as-achieved MnOx /C-y catalysts not only increased oxygen vacancies but also provided adsorption sites, which showed excellent activity and durability for mineralizing HCHO to CO2 and H2O at room temperature. The HCHO removal efficiency was up to 97.3% for 100 ppm of HCHO and 89.7% for 0.66 ppm of HCHO. Furthermore, no significant downward trend was detected even after four cycles. The rich Mn3+, surface oxygen vacancies, and reactive oxygen species were the main factors for HCHO removal. In situ DRIFTS study revealed that surface -OH accelerated the conversion and oxidation of the formed intermediates.
引用
收藏
页码:5125 / 5134
页数:10
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