Zeynep Balta, Esra Bilgin Simsek. Insights into the photocatalytic behavior of carbon-rich shungite-based WO3/TiO2 catalysts for enhanced dye and pharmaceutical degradation. New Carbon Mater., 2020, 35(4): 371-383. doi: 10.1016/S1872-5805(20)60495-4
Citation: Zeynep Balta, Esra Bilgin Simsek. Insights into the photocatalytic behavior of carbon-rich shungite-based WO3/TiO2 catalysts for enhanced dye and pharmaceutical degradation. New Carbon Mater., 2020, 35(4): 371-383. doi: 10.1016/S1872-5805(20)60495-4

Insights into the photocatalytic behavior of carbon-rich shungite-based WO3/TiO2 catalysts for enhanced dye and pharmaceutical degradation

doi: 10.1016/S1872-5805(20)60495-4
  • Received Date: 2020-04-02
  • Rev Recd Date: 2020-07-05
  • Publish Date: 2020-08-28
  • Carbon-rich shungite-based WO3/TiO2 catalysts were synthesized by a solvothermal method. The morphological, structural, optical and physical features of the catalysts were characterized by XPS, FTIR, Raman spectroscopy, SEM and UV-Vis diffuse-reflectance spectroscopy (DRS). The photocatalytic performance of the catalysts was investigated for the degradation of Orange II dye and pharmaceuticals under UV-A irradiation. SEM images show that the shungite surface is completely covered with WO3/TiO2 particles. Raman and XPS analyses demonstrate that the carbon-rich shungite is well-incorporated with the WO3 and TiO2. UV-Vis DRS indicates enhanced visible-light absorption and a lowered band gap (2.83 eV) for the catalysts. The degradation degree of Orange II increases with increasing shungite ratio, which is ascribed to a combined effect of adsorption and photocatalysis, and the improved light absorption and easy transfer of photogenerated holes and electrons across the interface of W/Ti. Mechanism studies indicate that the π-π conjugation between a dye molecule and the aromatic bonds of carbon materials are more dominant rather than columbic interactions, and that·O2- is the main species in Orange II degradation. However, the Orange II degradation efficiency is lowered in drinking water due to the photo-generated hole (h+)-scavenging effects by organic matter and salts and their competing adsorption with the target pollutant in the active sites on the catalyst surface. This work provides a possible use of the carbon-rich shungite as a natural carbon resource for the fabrication of carbon-based photocatalysts.
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