relation: https://khub.utp.edu.my/scholars/15236/
title: Development of Photo-Fenton oxidation as green strategy for phenol degradation enhancement via DMF-controlled TiO2nanotubes under various oxidizing agents
creator: Zulfiqar, M.
creator: Sufian, S.
creator: Rabat, N.E.
creator: Mansor, N.
description: Photo-Fenton oxidation has been successfully developed as an emerging strategy for the treatment of hazardous organics from synthetic wastewater. For this purpose, single-layered TNTs have been successfully synthesized through TiO2-P25 as a precursor, DMF and alkaline solution via a simple hydrothermal method at 180 °C for 3 h. The as-developed TNTs were characterized through XRD, TEM, BET surface area, FTIR, XPS and DRS techniques. TNTs produced in DMF provided a higher specific surface area of 214.021 m2/g with a narrow bandgap energy of 2.58 eV. The photoreactivity of DMF-controlled TNTs was investigated to catalyze the decomposition of oxidants namely FeCl3 and H2O2 to harvest free hydroxyl radicals and finally its significance for the remediation of phenol upto 98.77 in visible-light irradiation. To our knowledge, this research first investigated that solvent-controlled TNTs photocatalyst could successfully activate oxidizing agents for wastewater treatment. Langmuir-Hinshelwood kinetic model was successfully followed phenol degradation results providing the highest R2 upto 0.993. Several thermodynamic parameters as enthalpy = 34.15 kJ/mol, entropy = 71.22 kJ/mol K, Gibbs free energy = -10.10 to -11.13 kJ/mol and activation energy = 30.92 kJ/mol were recommended that phenol degradation method is favorable and spontaneous in nature. The increasing temperature was more suitable for phenol removal onto DMF-controlled TNTs. © 2020 Elsevier Ltd.
publisher: Elsevier Ltd
date: 2021
type: Article
type: PeerReviewed
identifier:   Zulfiqar, M. and Sufian, S. and Rabat, N.E. and Mansor, N.  (2021) Development of Photo-Fenton oxidation as green strategy for phenol degradation enhancement via DMF-controlled TiO2nanotubes under various oxidizing agents.  Journal of Environmental Chemical Engineering, 9 (1).   ISSN 22133437     
relation: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85098158002&doi=10.1016%2fj.jece.2020.104933&partnerID=40&md5=3fbc4ce2de2ab4210dc9171bd9005418
relation: 10.1016/j.jece.2020.104933
identifier: 10.1016/j.jece.2020.104933