Background Purpose: Photocatalytic water splitting for hydrogen evolution is a potential way to solve many energy and environmental issues. Developing visible-light-active photocatalysts to efficiently utilize sunlight and finding proper ways to improve photocatalytic activity for H2 evolution have always been hot topics for research. This study attempts to expand the use of sunlight and to enhance the photocatalytic activity of TiO2 by N doping and Au loading.
View Article and Find Full Text PDFPhotocatalytic oxidation (PCO) of toluene and benzaldehyde in indoor air by N doped TiO2 (N-TiO2) was conducted under UV irradiation of 254 nm. The intermediates were identified and monitored on real-time by proton transfer reaction-mass spectrometry. The health risks of PCO of toluene and benzaldehyde were assessed based on health risk influence index (eta).
View Article and Find Full Text PDFTo evaluate the health risk of vacuum ultraviolet (VUV) photolysis of naphthalene (NP) in indoor air, intermediates were detected by gas chromatograph-mass spectrometry and proton transfer reaction-mass spectrometry. Results showed that 13 volatile organic compounds (VOCs) in gas phase and five semi-volatile organic compounds (SVOCs) in oil phase were the main intermediates. VUV photolysis pathways of NP can be divided into five stages including functionalization, partition, condensation, fragmentation, and mineralization.
View Article and Find Full Text PDFConcentrations of 13 gaseous intermediates in photocatalytic oxidation (PCO) of toluene in indoor air were determined in real-time by proton transfer reaction mass spectrometry and desorption intensities of 7 adsorbed intermediates on the surface of photocatalysts were detected by temperature-programmed desorption-mass spectrometry. Effects of relative humidity (RH), photocatalysts, and vacuum ultraviolet (VUV) irradiation on the distribution and category of the intermediates and health risk influence index (η) were investigated. RH enhances the formation rate of hydroxide radicals, leading to more intermediates with higher oxidation states in gas phase.
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