Issue 34, 2024, Issue in Progress

Harnessing potassium peroxymonosulfate activation of WO3/diatomite composites for efficient photocatalytic degradation of tetracycline

Abstract

The increasing prevalence of pharmaceutical contaminants in aquatic ecosystems poses profound challenges for both environmental sustainability and public health. Addressing this pressing issue requires the development of innovative, cost-effective, and efficient remediation approaches. Here we report the synthesis of WO3/diatomite composites and their photocatalytic degradation in conjunction with potassium peroxymonosulfate (PMS) activation. By leveraging the synergistic effects, we observe a remarkable degradation of tetracycline, a significant pharmaceutical contaminant, under visible light. Analytically, we have elucidated the driving factors for the enhanced performance, emphasizing the optimal amount of WO3 (10%) in the composite and PMS concentration (3 mM). Specifically, the WO3/diatomite catalyst presents a degradation rate of 80.75% tetracycline (40 mg L−1) after 180 min of visible light irradiation. Also, we elucidate the primary roles of ˙SO4 radicals in driving the photocatalytic reaction using free radical trapping studies. Our approach not only offers a direct solution to controlling pharmaceutical contamination but also opens new possibilities for advancing the design of composite-based photocatalysts by taking advantage of nature-derived materials.

Graphical abstract: Harnessing potassium peroxymonosulfate activation of WO3/diatomite composites for efficient photocatalytic degradation of tetracycline

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Article information

Article type
Paper
Submitted
18 Jun 2024
Accepted
04 Aug 2024
First published
09 Aug 2024
This article is Open Access
Creative Commons BY license

RSC Adv., 2024,14, 25019-25030

Harnessing potassium peroxymonosulfate activation of WO3/diatomite composites for efficient photocatalytic degradation of tetracycline

T. L. Nguyen, H. H. Tran, T. C. Huynh, K. T. Le, T. M. Cao and V. V. Pham, RSC Adv., 2024, 14, 25019 DOI: 10.1039/D4RA04447A

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