Visible light driven ZnFe2O4 for the degradation of oxytetracycline in the presence of HSO5− at semi-pilot scale and additional H2 production
Document Type
Article
Source of Publication
Chemical Engineering Journal
Publication Date
10-15-2024
Abstract
This study investigated the synthesis of visible light driven ZnFe2O4 for photocatalytic degradation of oxytetracycline (OTC) in a continuous flow reactor and production of hydrogen (H2). OTC is widely used as a medication and found to create severe health and environmental issues. The use of advanced characterization techniques proved successful formation of ZnFe2O4 which was found to be reusable, stable, highly crystalline, and nano-sized. The prepared ZnFe2O4 caused 60% removal of OTC and removal efficiency of the latter was promoted to 85% by adding HSO5– with ZnFe2O4 at 240 min employing reactor flow rate of 0.1 L/min and concentrations of ZnFe2O4, OTC, and HSO5– as 1.0 g/L, 20 mg/L, and 100 mg/L, respectively. The addition of HSO5– was found to give hydroxyl radical (•OH) and sulfate radical (SO4•−) and the latter caused degradation of OTC into degradation products. The removal of OTC was promoted by factors facilitating the rate of formation of •OH and SO4•−. The ZnFe2O4 proved effective in photocatalytic H2 production and showed H2 production rate of 23.4 μmol h−1 g−1. The results suggest that ZnFe2O4 could be used as an economically viable technology for emerging pollutants degradation and green energy production.
DOI Link
ISSN
Publisher
Elsevier BV
Volume
498
Disciplines
Environmental Chemistry
Keywords
Emerging pharmaceuticals pollutants, Green economy, Green H production 2, Water treatment, ZnFe O photocatalyst 2 4
Scopus ID
Recommended Citation
Iqbal, Jibran; Shah, Noor S.; Ali Khan, Javed; Ibrahim, Anood; Masood Pirzada, Bilal; Naushad, Mu; and Han, Changseok, "Visible light driven ZnFe2O4 for the degradation of oxytetracycline in the presence of HSO5− at semi-pilot scale and additional H2 production" (2024). All Works. 6777.
https://zuscholars.zu.ac.ae/works/6777
Indexed in Scopus
yes
Open Access
no