4.4 Article

Enhanced photocatalytic treatment using plasmonic Ag@Ag3PO4/Ag@AgCl nanophotocatalyst for simultaneous degradation of multiple parabens and UV-filters in various aquatic environments under visible light irradiation

Journal

PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES
Volume 21, Issue 9, Pages 1601-1616

Publisher

SPRINGERNATURE
DOI: 10.1007/s43630-022-00243-x

Keywords

Photodegradation; Nanophotocatalyst; Parabens; UV filters; Optimization; SPE-GC-MS

Funding

  1. Research Council of Chemistry and Chemical Engineering Research Center (CCERCI)

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This study focused on the simultaneous photocatalytic degradation of different parabens and UV filters using a novel double plasmonic nanophotocatalyst. The nanophotocatalyst showed superior activity compared to individual nanoparticles due to the presence of two simultaneous surface plasmon resonances and a hetero-junction structure. Superoxide radicals were identified as the key reactive species. The degradation process was further investigated and optimized in different water matrices.
In this study, simultaneous photocatalytic degradation of different parabens (methyl-, ethyl-, propyl-, and butyl paraben) and UV filters (benzophenone-3, 4-methylbenzylidene camphor, 2-ethylhexyl 4-(dimethylamino) benzoate, ethylhexyl methoxy-cinnamate and octocrylene) in water matrices was performed under visible light irradiation using novel double plasmonic Ag@Ag3PO4/Ag@AgCl nanophotocatalyst, synthesized by an easy and fast photochemical conversion and photo-reduction. It was found that the nanophotocatalyst with appropriate mole ratio of Ag@Ag3PO4/Ag@AgCl (1:3) showed superior photocatalytic activity than individual plasmonic nanoparticles. This is because there are two simultaneous surface plasmon resonances (SPR) generated by the metallic Ag nanoparticles, in addition to the hetero-junction structure formed at the interface between Ag@Ag3PO4 and Ag@AgCl. The structures of the synthesized photocatalysts were characterized, and the principal reactive oxygen species in the photocatalytic process were identified via a trapping experiment, confirming superoxide radicals (center dot O-2(-)) as the key reactive species of the photocatalytic system. The process of photodegradation of the target pollutants was monitored using an optimized method that incorporated solid-phase extraction in combination with gas chromatography-mass spectrometry. The simultaneous photodegradation process was modeled and optimized using central composite design. The kinetic study revealed that the degradation process over Ag@Ag3PO4(30%)/Ag@AgCl(70%) under visible light followed a pseudo-first-order kinetic model. The simultaneous degradation of target compounds was further investigated in sewage treatment plant effluent as well as tap water. It was found that the matrix constituents can reduce the photodegradation efficiency, especially in the case of highly contaminated samples. [GRAPHICS] .

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