Faculty of Humanities and Sciences
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Publication Open Access Efficient photocatalysis of carbon coupled TiO2 to degrade pollutants in wastewater – A review(Elsevier, 2022-08-27) Thambiliyagodage, CWater pollution caused by human activities is a monumental problem that the world is facing today. The use of polluted water for domestic, industrial, and agricultural applications creates severe hazardous issues. Therefore, decontamination of polluted water is greatly important. The advanced oxidation process is preferred to purify contaminated water as the pollutants are completely degraded to harmless products. TiO2 is the most widely researched photocatalyst due to its chemical stability, low cost and eco-friendliness. However, the use of TiO2 is limited as it is only sensitive to UV range due to its high band gap (3.0 eV for rutile) and the possible electron-hole pair recombination. TiO2 has been coupled with carbon-based materials to enhance photocatalytic activity by enhancing charge separation and visible light absorption. This review summarizes the recent use of TiO2 coupled to activated carbon, carbon nanotubes, graphene derivatives, and g-C3N4 to degrade different pollutants found in water including dyes, pesticides, pharmaceuticals, phenols and heavy metals. The advantages and disadvantages of using each carbon-based material are discussed. Further, the challenges and opportunities associated with all the materials are presented. Finally, recommendations and possible future outlooks are briefed in this review.Publication Open Access Efficient Visible-Light Photocatalysis and Antibacterial Activity of TiO2-Fe3C-Fe-Fe3O4/Graphitic Carbon Composites Fabricated by Catalytic Graphitization of Sucrose Using Natural Ilmenite(American Chemical Society, 2022-07-26) Thambiliyagodage, C; Usgodaarachchi, L; Jayanetti, M; Liyanaarachchi, C; Kandanapitiye, M; Vigneswaran, SDyes in wastewater are a serious problem that needs to be resolved. Adsorption coupled photocatalysis is an innovative technique used to remove dyes from contaminated water. Novel composites of TiO2-Fe3C-Fe-Fe3O4dispersed on graphitic carbon were fabricated using natural ilmenite sand as the source of iron and titanium, and sucrose as the carbon source, which were available at no cost. Synthesized composites were characterized by X-ray diffractometry (XRD), Raman spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray fluorescence spectroscopy (XRF), and diffuse reflectance UV-visible spectroscopy (DRS). Arrangement of nanoribbons of graphitic carbon with respect to the nanomaterials was observed in TEM images, revealing the occurrence of catalytic graphitization. Variations in the intensity ratio (ID/IG), Laand LD, calculated from data obtained from Raman spectroscopy suggested that the level of graphitization increased with an increased loading of the catalysts. SEM images show the immobilization of nanoplate microballs and nanoparticles on the graphitic carbon matrix. The catalyst surface consists of Fe3+and Ti4+as the metal species, with V, Mn, and Zr being the main impurities. According to DRS spectra, the synthesized composites absorb light in the visible region efficiently. Fabricated composites effectively adsorb methylene blue via π-πinteractions, with the absorption capacities ranging from 21.18 to 45.87 mg/g. They were effective in photodegrading methylene blue under sunlight, where the rate constants varied in the 0.003-0.007 min-1range. Photogenerated electrons produced by photocatalysts captured by graphitic carbon produce O2•-radicals, while holes generate OH•radicals, which effectively degrade methylene blue molecules. TiO2-Fe3C-Fe-Fe3O4/graphitic carbon composites inhibited the growth of Escherichia coli (69%) and Staphylococcus aureus (92%) under visible light. Synthesized novel composites using natural materials comprise an ecofriendly, cost-effective solution to remove dyes, and they were effective in inhibiting the growth of Gram-negative and Gram-positive bacteria.
