Enhanced photocatalytic degradation of organic pollutants using Fe2O3-TiO2 composites
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Faculty of Applied Sciences, South Eastern University of Sri Lanka, Sammanthurai.
Abstract
This study presents the synthesis and evaluation of Fe₂O₃–TiO₂ composites for the
photocatalytic degradation of organic pollutants, using methylene blue (MB) as a model dye
under ultraviolet (UV) light irradiation. The composites were prepared via a simple, cost-
effective sol–gel method, ensuring uniform mixing and controlled particle properties.
Structural and functional group characterization was performed using X-ray diffraction
(XRD) and Fourier-transform infrared spectroscopy (FTIR). XRD confirmed the presence of
anatase- phase TiO₂ and hematite-phase Fe₂O₃, while FTIR spectra indicated characteristic Ti–
O and Fe–O bonds, suggesting strong interfacial interactions. Photocatalytic performance was
systematically evaluated by varying pH (3, 6.09, 11), initial MB concentration (5, 10, 15
ppm), and catalyst dosage (0.5, 1.0, 1.5 g L⁻¹). The highest degradation efficiency (90.28%)
was achieved at pH 11, 10 ppm dye concentration, and 1 g L⁻¹ catalyst dosage. Kinetic
analysis revealed that the degradation followed pseudo-first-order kinetics, with a rate
constant of 0.0198 min⁻¹. Control experiments confirmed that significant degradation
occurred only when both UV light and the catalyst were present, verifying true photocatalytic
activity. The enhanced performance is attributed to Fe₂O₃-induced charge separation, which
reduces electron–hole recombination in TiO₂, promoting reactive oxygen species generation.
The results indicate that Fe₂O₃–TiO₂ composites are efficient, stable, and potentially reusable
catalysts, suitable for textile wastewater treatment and adaptable for broader environmental
applications.
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Conference Proceedings of 14th Annual Science Research Session – 2025 on “NEXT-GEN SOLUTIONS: Bridging Science and Sustainability” on October 30th 2025. Faculty of Applied Sciences, South Eastern University of Sri Lanka, Sammanthurai.. pp. 18.
