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Degradation of Minocycline by the Adsorption–Catalysis Multifunctional PVDF–PVP–TiO(2) Membrane: Degradation Kinetics, Photocatalytic Efficiency, and Toxicity of Products

The photocatalytic degradation of minocycline was studied by using polyvinylidene fluoride–polyvinylpyrrolidone–TiO(2) (PVDF–PVP–TiO(2)) fiber mats prepared by an electrospinning technology. The influences of the TiO(2) dosage, minocycline concentrations, inorganic anions, pH values, and dissolved o...

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Detalles Bibliográficos
Autores principales: Zhou, Chengzhi, Sun, Yanlong, Zhang, Fan, Wu, Yuandong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656511/
https://www.ncbi.nlm.nih.gov/pubmed/34886061
http://dx.doi.org/10.3390/ijerph182312339
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author Zhou, Chengzhi
Sun, Yanlong
Zhang, Fan
Wu, Yuandong
author_facet Zhou, Chengzhi
Sun, Yanlong
Zhang, Fan
Wu, Yuandong
author_sort Zhou, Chengzhi
collection PubMed
description The photocatalytic degradation of minocycline was studied by using polyvinylidene fluoride–polyvinylpyrrolidone–TiO(2) (PVDF–PVP–TiO(2)) fiber mats prepared by an electrospinning technology. The influences of the TiO(2) dosage, minocycline concentrations, inorganic anions, pH values, and dissolved organic matter (DOM) concentrations on the degradation kinetics were investigated. A mass of 97% minocycline was degraded in 45 min at 5% TiO(2) dosage. The corresponding decomposition rate constant was 0.069 min(−1). The inorganic anions affected the minocycline decomposition in the order of HCO(3)(−) > Cl(−) > SO(4)(2−) > NO(3)(−), which was confirmed by the results of electron spin resonance (ESR) spectra. The lowest electrical energy per order (E(EO)) was 6.5 Wh/L. Over five cycles, there was no change in the photocatalytic performance of the degrading minocycline. Those investigations suggested that effective degradation of minocycline could be reached in the PVDF–PVP–TiO(2) fiber mats with a low energy consumption, good separation and, good recovery. Three photocatalytic decomposition pathways of minocycline were proposed: (i) hydroxyl substitution of the acylamino group; (ii) hydroxyl substitution of the amide group, and (iii) a cleavage of the methyl groups and further oxidation of the amino group by OH. Potential risks caused by TP159 and TP99 should not be ignored, while the TP90 are nontoxic. Tests indicated that the toxicity of the photocatalytic process may be persistent if minocycline and its products were not mineralized completely.
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spelling pubmed-86565112021-12-10 Degradation of Minocycline by the Adsorption–Catalysis Multifunctional PVDF–PVP–TiO(2) Membrane: Degradation Kinetics, Photocatalytic Efficiency, and Toxicity of Products Zhou, Chengzhi Sun, Yanlong Zhang, Fan Wu, Yuandong Int J Environ Res Public Health Article The photocatalytic degradation of minocycline was studied by using polyvinylidene fluoride–polyvinylpyrrolidone–TiO(2) (PVDF–PVP–TiO(2)) fiber mats prepared by an electrospinning technology. The influences of the TiO(2) dosage, minocycline concentrations, inorganic anions, pH values, and dissolved organic matter (DOM) concentrations on the degradation kinetics were investigated. A mass of 97% minocycline was degraded in 45 min at 5% TiO(2) dosage. The corresponding decomposition rate constant was 0.069 min(−1). The inorganic anions affected the minocycline decomposition in the order of HCO(3)(−) > Cl(−) > SO(4)(2−) > NO(3)(−), which was confirmed by the results of electron spin resonance (ESR) spectra. The lowest electrical energy per order (E(EO)) was 6.5 Wh/L. Over five cycles, there was no change in the photocatalytic performance of the degrading minocycline. Those investigations suggested that effective degradation of minocycline could be reached in the PVDF–PVP–TiO(2) fiber mats with a low energy consumption, good separation and, good recovery. Three photocatalytic decomposition pathways of minocycline were proposed: (i) hydroxyl substitution of the acylamino group; (ii) hydroxyl substitution of the amide group, and (iii) a cleavage of the methyl groups and further oxidation of the amino group by OH. Potential risks caused by TP159 and TP99 should not be ignored, while the TP90 are nontoxic. Tests indicated that the toxicity of the photocatalytic process may be persistent if minocycline and its products were not mineralized completely. MDPI 2021-11-24 /pmc/articles/PMC8656511/ /pubmed/34886061 http://dx.doi.org/10.3390/ijerph182312339 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhou, Chengzhi
Sun, Yanlong
Zhang, Fan
Wu, Yuandong
Degradation of Minocycline by the Adsorption–Catalysis Multifunctional PVDF–PVP–TiO(2) Membrane: Degradation Kinetics, Photocatalytic Efficiency, and Toxicity of Products
title Degradation of Minocycline by the Adsorption–Catalysis Multifunctional PVDF–PVP–TiO(2) Membrane: Degradation Kinetics, Photocatalytic Efficiency, and Toxicity of Products
title_full Degradation of Minocycline by the Adsorption–Catalysis Multifunctional PVDF–PVP–TiO(2) Membrane: Degradation Kinetics, Photocatalytic Efficiency, and Toxicity of Products
title_fullStr Degradation of Minocycline by the Adsorption–Catalysis Multifunctional PVDF–PVP–TiO(2) Membrane: Degradation Kinetics, Photocatalytic Efficiency, and Toxicity of Products
title_full_unstemmed Degradation of Minocycline by the Adsorption–Catalysis Multifunctional PVDF–PVP–TiO(2) Membrane: Degradation Kinetics, Photocatalytic Efficiency, and Toxicity of Products
title_short Degradation of Minocycline by the Adsorption–Catalysis Multifunctional PVDF–PVP–TiO(2) Membrane: Degradation Kinetics, Photocatalytic Efficiency, and Toxicity of Products
title_sort degradation of minocycline by the adsorption–catalysis multifunctional pvdf–pvp–tio(2) membrane: degradation kinetics, photocatalytic efficiency, and toxicity of products
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656511/
https://www.ncbi.nlm.nih.gov/pubmed/34886061
http://dx.doi.org/10.3390/ijerph182312339
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