4.6 Article

Pilot-Scale Studies of WO3/S-Doped g-C3N4 Heterojunction toward Photocatalytic NOx Removal

期刊

MATERIALS
卷 15, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/ma15020633

关键词

photocatalysis; NOx removal; S-doped g-C3N4; WO3; scaling-up

资金

  1. National Centre for Research and Development [POIR.01.01.01-00-0071/20-00]

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In this study, a novel WO3/S-doped g-C3N4 nanocomposite was developed for efficient removal of NOx in the air through photocatalytic reactions. The photocatalytic tests were conducted in a continuous-flow photoreactor, which demonstrated that the composite exhibited high efficiency in converting NO2 and had good stability.
Due to the rising concentration of toxic nitrogen oxides (NOx) in the air, effective methods of NOx removal have been extensively studied recently. In the present study, the first developed WO3/S-doped g-C3N4 nanocomposite was synthesized using a facile method to remove NOx in air efficiently. The photocatalytic tests performed in a newly designed continuous-flow photoreactor with an LED array and online monitored NO2 and NO system allowed the investigation of photocatalyst layers at the pilot scale. The WO3/S-doped-g-C3N4 nanocomposite, as well as single components, were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller surface area analysis (BET), X-ray fluorescence spectroscopy (XRF), X-ray photoemission spectroscopy method (XPS), UV-vis diffuse reflectance spectroscopy (DR/UV-vis), and photoluminescence spectroscopy with charge carriers' lifetime measurements. All materials exhibited high efficiency in photocatalytic NO2 conversion, and 100% was reached in less than 5 min of illumination under simulated solar light. The effect of process parameters in the experimental setup together with WO3/S-doped g-C3N4 photocatalysts was studied in detail. Finally, the stability of the composite was tested in five subsequent cycles of photocatalytic degradation. The WO3/S-doped g-C3N4 was stable in time and did not undergo deactivation due to the blocking of active sites on the photocatalyst's surface.

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