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Prof. Charitha Jayaruk Thambiliyagodage

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https://orcid.org/0000-0003-0906-4441

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https://scholar.google.com/citations?user=kdc5vsQAAAAJ

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Prof. Charitha Jayaruk Thambiliyagodage

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Jayaruk is a graduate of the University of Colombo. He pursued his PhD in Chemistry from The University of Alabama, USA. He has specialized in Materials, Analytical and Physical Chemistry. Currently, he is working as an Assistant Professor at the Department of Applied Sciences, SLIIT. He is the coordinator of the BSc Biotechnology degree programme. He has been awarded the chartered chemist designation by the Institute of Chemistry, Ceylon. He supervises Postgraduate students at the University of Colombo and the University of Kelaniya and supervises undergraduate students at the Institute of Chemistry. He is interested in doing research on using nanomaterials in water purification and as antimicrobial reagents. Further, he is interested in researching on algae and plant materials for their pharmaceutical and cosmeceutical activities. He has specialized in many instruments like Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), X-Ray Diffractometer (XRD), X-Ray Photoelectron Spectrometer (XPS), Gas chromatograph-Mass spectrometer (GC-MS), Raman Spectrometer, FT-IR spectrometer, UV-Visible Spectrophotometer, Brunauer-Emmett-Teller (BET) surface area analyzer etc. He is interested in practical-based science education and believes in uplifting the research culture among upcoming scientists in the country.

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Application of nanomaterials for water purification Novel nanomaterials incorporated cosmeceuticals and pharmaceuticals Natural material based neutraceuticals Alternative energy sources Novel packaging materials Environmental Chemistry

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search.filters.applied.f.isAuthorOfPublication: search.filters.isAuthorOfPublication.95d00db3-68ae-4943-bcef-3692a59bbcd5Author: search.filters.author.Liyanaarachchi, HAuthor: search.filters.author.Vigneswaran, S

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Now showing 1 - 4 of 4
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    PublicationOpen 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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    PublicationOpen Access
    Fabrication of Naturally Derived Chitosan and Ilmenite Sand-Based TiO2/Fe2O3/Fe-N-Doped Graphitic Carbon Composite for Photocatalytic Degradation of Methylene Blue under Sunlight
    (MDPI, 2023-04-01) Mendis, A; Thambiliyagodage, C; Ekanayake, G; Liyanaarachchi, H; Jayanetti, M; Vigneswaran, S
    first_pagesettingsOrder Article Reprints Open AccessArticle Fabrication of Naturally Derived Chitosan and Ilmenite Sand-Based TiO2/Fe2O3/Fe-N-Doped Graphitic Carbon Composite for Photocatalytic Degradation of Methylene Blue under Sunlight by Amavin Mendis 1,Charitha Thambiliyagodage 1,*ORCID,Geethma Ekanayake 1,Heshan Liyanaarachchi 1ORCID,Madara Jayanetti 1 andSaravanamuthu Vigneswaran 2,3,* 1 Faculty of Humanities and Sciences, Sri Lanka Institute of Information Technology, Malabe 10115, Sri Lanka 2 Faculty of Engineering and Information Technology, University of Technology Sydney, P.O. Box 123, Sydney, NSW 2007, Australia 3 Faculty of Sciences & Technology (RealTek), Norwegian University of Life Sciences, P.O. Box N-1432 Ås, Norway * Authors to whom correspondence should be addressed. Molecules 2023, 28(7), 3154; https://doi.org/10.3390/molecules28073154 Received: 15 March 2023 / Revised: 29 March 2023 / Accepted: 30 March 2023 / Published: 1 April 2023 (This article belongs to the Section Materials Chemistry) Download Browse Figures Versions Notes Abstract Fabrication of chitosan and ilmenite sand-based novel photocatalysts through the catalytic graphitization of chitosan is reported. Nanocomposites consisted of TiO2, Fe2O3 and Fe nanoparticles dispersed on a nitrogen-doped graphitic carbon framework. The surface area, pore volume and macropore structure of the carbon matrix is disturbed by the heterogeneously distributed nanoparticles. The extent of graphitization expanded with increasing metal loading as indicated by variation in the ID/IG ratio. The nanomaterial’s surface consists of Fe3+ and Ti4+, and graphitic, pyridinic and pyrrolic nitrogen were found in the carbon matrix. The band gap values of the composites varied in the 2.06–2.26 eV range. The photocatalytic activity of the synthesized nanomaterials was determined, and the highest rate constant for the photodegradation of methylene blue under sunlight was 4.4 × 10−3 min−1, which resulted with 10 mg/L MB and 25 mg of the best-performing catalyst. The rate constant rose with increasing concentrations of persulfate added to the medium. The rate constant greatly diminished with the addition of isopropyl alcohol as it scavenged hydroxyl radicals. The presence of co-pollutants including Pb2+, rhodamine B, PO43− and Cl− curtailed the rate of reaction. The activity reduced with an increasing number of uses of the catalyst.
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    PublicationOpen Access
    Persulfate assisted photocatalytic and antibacterial activity of TiO2–CuO coupled with graphene oxide and reduced graphene oxide
    (https://www.nature.com, 2024-05-31) Thambiliyagodage, C; Liyanaarachchi, H; Jayanetti, M; Ekanayake, G; Mendis, A; Samarakoon, U; Vigneswaran, S
    Photocatalysts of TiO2–CuO coupled with 30% graphene oxide (GO) were hydrothermally fabricated, which varied the TiO2 to CuO weight ratios to 1:4, 1:2, 1:1, 2:1 and 4:1 and reduced to form TiO2–CuO/reduced graphene oxide (rGO) photocatalysts. They were characterized using XRD, TEM, SEM, XPS, Raman, and DRS technologies. TiO2–CuO composites and TiO2–CuO/GO degrade methylene blue when persulfate ions are present. Persulfate concentration ranged from 1, 2, 4 to 8 mmol/dm−3 in which the highest activity of 4.4 × 10–2 and 7.35 × 10–2 min−1 was obtained with 4 mmol/dm−3 for TiO2–CuO (1:4) and TiO2–CuO/GO (1:1), respectively. The presence of EDTA and isopropyl alcohol reduced the photodegradation. TiO2–CuO coupled with rGO coagulates methylene blue in the presence of persulfate ions and such coagulation is independent of light. The catalyst dosage and the concentration of the dye were varied for the best-performing samples. The antibacterial activity of the synthesized samples was evaluated against the growth of Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and Klebsiella pneumonia. Ti:Cu (1:2)-GO and Ti:Cu (1:4)-GO had the highest antibacterial activity against K. pneumoniae (16.08 ± 0.14 mm), P. aeruginosa (22.33 ± 0.58 mm), E. coli (16.17 ± 0.29 mm) and S. aureus (16.08 ± 0.88).
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    PublicationOpen 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.