Immobilization of Polymeric g-C3N4 on Structured Ceramic Foam for Efficient Visible Light Photocatalytic Air Purification with Real Indoor Illumination

被引:450
作者
Dong, Fan [1 ]
Wang, Zhenyu [1 ]
Li, Yuhan [1 ]
Ho, Wing-Kei [2 ]
Lee, S. C. [3 ]
机构
[1] Chongqing Technol & Business Univ, Coll Environm & Biol Engn, Chongqing Key Lab Catalysis & Funct Organ Mol, Chongqing 400067, Peoples R China
[2] Hong Kong Inst Educ, Dept Sci & Environm Studies, Tai Po, Hong Kong, Peoples R China
[3] Hong Kong Polytech Univ, Dept Civil & Environm Engn, Kowloon, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHITIC CARBON NITRIDE; GROWTH-MECHANISM; HYDROGEN EVOLUTION; NO; REMOVAL; SEMICONDUCTORS; MICROSPHERES; NANOSHEETS; PERFORMANCE; WATER;
D O I
10.1021/es502290f
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The immobilization of a photocatalyst on a proper support is pivotal for practical environmental applications. In this work, graphitic carbon nitride (g-C3N4) as a rising visible light photocatalyst was first immobilized on structured Al2O3 ceramic foam by a novel in situ approach. Immobilized g-C3N4 was applied for photocatalytic removal of 600 ppb level NO in air under real indoor illumination of an energy-saving lamp. The photocatalytic activity of immobilized g-C3N4 was gradually improved as the pyrolysis temperature was increased from 450 to 600 degrees C. The optimized conditions for g-C3N4 immobilization on Al2O3 supports can be achieved at 600 degrees C for 2 h. The NO removal ratio could reach up to 77.1%, exceeding that of other types of well-known immobilized photocatalysts. Immobilized g-C3N4 was stable in activity and can be used repeatedly without deactivation. The immobilization of g-C3N4 on Al2O3 ceramic foam was found to be firm enough to overwhelm the continuous air flowing, which can be ascribed to the special chemical interaction between g-C3N4 and Al2O3. On the basis of the 5,5'-dimethyl-1-pirroline-N-oxide electron spin resonance (DMPO ESR) spin trapping and reaction intermediate monitoring, the active species produced from g-C3N4 under illumination were confirmed and the reaction mechanism of photocatalytic NO oxidation by g-C3N4 was revealed. The present work could provide new perspectives for promoting large-scale environmental applications of supported photocatalysts.
引用
收藏
页码:10345 / 10353
页数:9
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