Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/35847
Title: Immobilization of polymeric g-C3N4 on structured ceramic foam for efficient visible light photocatalytic air purification with real indoor illumination
Authors: Dong, F
Wang, ZY
Li, YH
Ho, WK
Lee, SC 
Issue Date: 2014
Publisher: American Chemical Society
Source: Environmental science & technology, 2014, v. 48, no. 17, p. 10345-10353 How to cite?
Journal: Environmental science & technology 
Abstract: 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.
URI: http://hdl.handle.net/10397/35847
ISSN: 0013-936X (print)
1520-5851 (online)
DOI: 10.1021/es502290f
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