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Fabrication of AQ2S/GR composite photosensitizer for the simulated solar light-driven degradation of sulfapyridine

Authors :
Xu-Dong Qin
Cheng-Xin Chen
Ya-Ni Zang
Xin-Lei Gao
Shuang-Yang Zhao
Nanqi Ren
Jie Ding
Zhao Song
Shan-Shan Yang
Source :
Environmental Science and Ecotechnology, Vol 8, Iss, Pp 100111-(2021)
Publication Year :
2021
Publisher :
Elsevier, 2021.

Abstract

Chlorination has been intensively investigated for use in water disinfection and pollutant elimination due to its efficacy and convenience; however, the generation and transportation of chlorine and hypochlorite are energy-consuming and complicated. In this study, a novel binary photosensitizer consisting of anthraquinone-2-sulfonate (AQ2S) and graphene was synthesized via a π-π stack adsorption method; this compound could allow for the chlorination of organic pollutants using on-site chlorine generation. In this photosensitive degradation process, sulfapyridine (SPY) was selected as a model pollutant and was decomposed by the reactive species (Cl2•-, Cl• and O2•-) generated during the photosensitive oxidation of chloride. The synthesized AQ2S/graphene exhibited superior activity, and the degradation rate of SPY was over 90 % after 12 h of visible light irradiation with a kinetic constant of 0.2034h−1. Results show that 20 mg AQ2S/GR at a 21 % weight percentage of AQ2S in a pH 7 SPY solution with 1 mol/L Cl− achieved the highest kinetics rate at 0.353 h−1. Free radical trapping experiments demonstrated that Cl2•- and O2•- were the dominant species involved in SPY decomposition under solar light. The reusability and stability of this composite were verified by conducting a cycle experiment over five successive runs. The capacity of photodegradation still remained over 90 % after these 5 runs. The current study provides an energy-efficient and simple-operational approach for water phase SPY control.

Details

Language :
English
ISSN :
26664984
Volume :
8
Database :
OpenAIRE
Journal :
Environmental Science and Ecotechnology
Accession number :
edsair.doi.dedup.....bdb766300a4e2545a3b3065ac62c1336