School of Natural Sciences

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Open Access
Kinetics and Thermodynamics Study of Methylene Blue Adsorption to Sucrose- and Urea-Derived Nitrogen-Enriched, Hierarchically Porous Carbon Activated by KOH and H3PO4
(American Chemical Society, 2023-04-27) Liyanaarachchi, H; Thambiliyagodage, C; Lokuge, H; Vigneswaran, S
Hierarchically porous nitrogen-enriched carbon materials synthesized by polymerization of sucrose and urea (SU) were activated by KOH and H3PO4 (SU-KOH and SU-H3PO4, respectively). Characterization was undertaken and the synthesized materials were tested for their ability to adsorb methylene blue (MB). Scanning electron microscopic images along with the Brunauer−Emmett−Teller (BET) surface area analysis revealed the presence of a hierarchically porous system. X-ray photoelectron spectroscopy (XPS) confirms the surface oxidation of SU upon activation with KOH and H3PO4. The best conditions for removing dyes utilizing both activated adsorbents were determined by varying the pH, contact time, adsorbent dosage, and dye concentration. Adsorption kinetics were evaluated, and the adsorption of MB followed second-order kinetics, suggesting the chemisorption of MB to both SU-KOH and SUH3PO4. Times taken to reach the equilibrium by SU-KOH and SU-H3PO4 were 180 and 30 min, respectively. The adsorption isotherm data were fitted to the Langmuir, Freundlich, Temkin, and Dubinin models. Data were best described by the Temkin isotherm model for SU-KOH and the Freundlich isotherm model for SU-H3PO4. Thermodynamics of the adsorption of MB to the adsorbent was determined by varying the temperature in the range of 25−55 °C. Adsorption of MB increased with increasing temperature, suggesting that the adsorption process is endothermic. The highest adsorption capacities of SU-KOH and SU-H3PO4 (1268 and 897 mg g−1 , respectively) were obtained at 55 °C. Synthesized adsorbents were effective in removing MB for five cycles with some loss in activity. The results of this study show that SU activated by KOH and H3PO4 are environmentally benign, favorable, and effective adsorbents for MB adsorption.
Open Access
Recent Advances in Chitosan-Based Applications—A Review
(MDPI, 2023-03-03) Thambiliyagodage, C; Jayanetti, M; Mendis, A; Ekanayake, G; Liyanaarachchi, H; Liyanaarachchi, S
Chitosan derived from chitin has gathered much interest as a biopolymer due to its known and possible broad applications. Chitin is a nitrogen-enriched polymer abundantly present in the exoskeletons of arthropods, cell walls of fungi, green algae, and microorganisms, radulae and beaks of molluscs and cephalopods, etc. Chitosan is a promising candidate for a wide variety of applications due to its macromolecular structure and its unique biological and physiological properties, including solubility, biocompatibility, biodegradability, and reactivity. Chitosan and its derivatives have been known to be applicable in medicine, pharmaceuticals, food, cosmetics, agriculture, the textile and paper industries, the energy industry, and industrial sustainability. More specifically, their use in drug delivery, dentistry, ophthalmology, wound dressing, cell encapsulation, bioimaging, tissue engineering, food packaging, gelling and coating, food additives and preservatives, active biopolymeric nanofilms, nutraceuticals, skin and hair care, preventing abiotic stress in flora, increasing water availability in plants, controlled release fertilizers, dye-sensitised solar cells, wastewater and sludge treatment, and metal extraction. The merits and demerits associated with the use of chitosan derivatives in the above applications are elucidated, and finally, the key challenges and future perspectives are discussed in detail.
Open Access
Fabrication of r-GO/GO/α-Fe2O3/Fe2TiO5 Nanocomposite Using Natural Ilmenite and Graphite for Efficient Photocatalysis in Visible Light
(MDPI, 2023-01) Usgodaarachchi, L; Jayanetti, M; Thambiliyagodage, C; Liyanaarachchi, H; Vigneswaran, S
Hematite (α-Fe2O3) and pseudobrookite (Fe2TiO5) suffer from poor charge transport and a high recombination effect under visible light irradiation. This study investigates the design and production of a 2D graphene-like r-GO/GO coupled α-Fe2O3/Fe2TiO5 heterojunction composite with better charge separation. It uses a simple sonochemical and hydrothermal approach followed by L-ascorbic acid chemical reduction pathway. The advantageous band offset of the α-Fe2O3/Fe2TiO5 (TF) nanocomposite between α-Fe2O3 and Fe2TiO5 forms a Type-II heterojunction at the Fe2O3/Fe2TiO5 interface, which efficiently promotes electron-hole separation. Importantly, very corrosive acid leachate resulting from the hydrochloric acid leaching of ilmenite sand, was successfully exploited to fabricate α-Fe2O3/Fe2TiO5 heterojunction. In this paper, a straightforward synthesis strategy was employed to create 2D graphene-like reduced graphene oxide (r-GO) from Ceylon graphite. The two-step process comprises oxidation of graphite to graphene oxide (GO) using the improved Hummer’s method, followed by controlled reduction of GO to r-GO using L-ascorbic acid. Before the reduction of GO to the r-GO, the surface of TF heterojunction was coupled with GO and was allowed for the controlled L-ascorbic acid reduction to yield r-GO/GO/α-Fe2O3/Fe2TiO5 nanocomposite. Under visible light illumination, the photocatalytic performance of the 30% GO/TF loaded composite material greatly improved (1240 Wcm−2). Field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM) examined the morphological characteristics of fabricated composites. X-ray photoelectron spectroscopy (XPS), Raman, X-ray diffraction (XRD), X-ray fluorescence (XRF), and diffuse reflectance spectroscopy (DRS) served to analyze the structural features of the produced composites. © 2022 by the authors.

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