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Unraveling the mechanisms of room-temperature catalytic degradation of indoor formaldehyde and its biocompatibility on colloidal TiO2-supported MnOx-CeO2
Li, Haiwei1; Huang, Tingting2; Lu, Yanfeng2; Cui, Long1; Wang, Zhenyu2,3; Zhang, Chaofeng2; Lee, Shuncheng1; Huang, Yu2; Cao, Junji2,3; Ho, Wingkei4
2018-05-01
发表期刊ENVIRONMENTAL SCIENCE-NANO
卷号5期号:5页码:1130-1139
文章类型Article
摘要This work overcomes the limitations in room-temperature and moisture-dependent activity of transition metal oxide-based catalysts for sub-ppm formaldehyde removal. The active site exposure and selfassembly hydrophilicity were highlighted in MnOx-CeO2 (MCO) nanospheres after the loading of colloidal 2.1 wt% TiO2 particles (TO-MCO). Approximately 57% (relative humidity = 72%) and 41% (dry air) recycling catalytic activities at 35 degrees C were achieved. Our results proved that surface electron transfer, which was previously weakened because of the loss of surface oxygen species and unsuitable defect-site depositions of low active ions, in the MCO catalyst was recovered via the dispersion of hydrophilic Ti-O groups. This electron transfer was also strongly correlated with the specific surface area, porosity, and oxidation states of transition metals. The greater active site exposure derived from the cyclic electron transfer eventually enhanced the HCHO chemisorption and participation of oxygen species on the surface of TO-MCO throughout the bimetallic (Mn-Ce) dismutation reactions. The abundant superoxide radicals that were activated by these oxygen species prompted a nucleophilic attack on carbonyl bonds. Direct photoionization mass spectrometry determined formic acid, dioxirane (minor), and HOCH2OOH (little) as intermediates governing the HCHO selectivity to CO2. The cytotoxicity of catalysts exposed to yeast cells was evaluated for their potential environmentally friendly application indoors.
WOS标题词Science & Technology ; Physical Sciences ; Life Sciences & Biomedicine
DOI10.1039/c8en00176f
关键词[WOS]OXYGEN REDUCTION REACTION ; AMBIENT-TEMPERATURE ; CRIEGEE INTERMEDIATE ; OXIDATION ; REMOVAL ; NO ; SURFACE ; OXIDE ; MNO2 ; AIR
收录类别SCI
语种英语
WOS研究方向Chemistry ; Environmental Sciences & Ecology ; Science & Technology - Other Topics
WOS类目Chemistry, Multidisciplinary ; Environmental Sciences ; Nanoscience & Nanotechnology
WOS记录号WOS:000432684200009
引用统计
被引频次:26[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.ieecas.cn/handle/361006/5145
专题粉尘与环境研究室
作者单位1.Hong Kong Polytech Univ, Dept Civil & Environm Engn, Hong Kong, Hong Kong, Peoples R China
2.Chinese Acad Sci, Inst Earth Environm, Key Lab Aerosol Chem & Phys, Xian 710061, Shaanxi, Peoples R China
3.Xi An Jiao Tong Univ, Sch Human Settlements & Civil Engn, Xian 710049, Shaanxi, Peoples R China
4.Educ Univ Hong Kong, Dept Sci & Environm Studies, Hong Kong, Hong Kong, Peoples R China
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Li, Haiwei,Huang, Tingting,Lu, Yanfeng,et al. Unraveling the mechanisms of room-temperature catalytic degradation of indoor formaldehyde and its biocompatibility on colloidal TiO2-supported MnOx-CeO2[J]. ENVIRONMENTAL SCIENCE-NANO,2018,5(5):1130-1139.
APA Li, Haiwei.,Huang, Tingting.,Lu, Yanfeng.,Cui, Long.,Wang, Zhenyu.,...&Ho, Wingkei.(2018).Unraveling the mechanisms of room-temperature catalytic degradation of indoor formaldehyde and its biocompatibility on colloidal TiO2-supported MnOx-CeO2.ENVIRONMENTAL SCIENCE-NANO,5(5),1130-1139.
MLA Li, Haiwei,et al."Unraveling the mechanisms of room-temperature catalytic degradation of indoor formaldehyde and its biocompatibility on colloidal TiO2-supported MnOx-CeO2".ENVIRONMENTAL SCIENCE-NANO 5.5(2018):1130-1139.
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