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M-Carboxylic Acid Induced Formation of New Coordination Polymers for Efficient Photocatalytic Degradation of Ciprofloxacin

Four new 2–3D materials were designed and synthesized by hydrothermal methods, namely, {[(L1·Cu·2H(2)O) (4,4-bipy)(0.5)] (β-Mo(8)O(26))(0.5)·H(2)O} (1), {[(L1·Cu)(2)·(4,4-bipy)] (Mo(5)O(16))} (2), {Co(L1)(2)}(n) (3), and {[(L1)(2)][β-Mo(8)O(26)](0.5)·5H(2)O} (4). [L1=5-(4-aminopyridine) isophthalic...

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Autores principales: Li, Jian, Wang, Xiaojia, Niu, Yunyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693974/
https://www.ncbi.nlm.nih.gov/pubmed/36431831
http://dx.doi.org/10.3390/molecules27227731
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author Li, Jian
Wang, Xiaojia
Niu, Yunyin
author_facet Li, Jian
Wang, Xiaojia
Niu, Yunyin
author_sort Li, Jian
collection PubMed
description Four new 2–3D materials were designed and synthesized by hydrothermal methods, namely, {[(L1·Cu·2H(2)O) (4,4-bipy)(0.5)] (β-Mo(8)O(26))(0.5)·H(2)O} (1), {[(L1·Cu)(2)·(4,4-bipy)] (Mo(5)O(16))} (2), {Co(L1)(2)}(n) (3), and {[(L1)(2)][β-Mo(8)O(26)](0.5)·5H(2)O} (4). [L1=5-(4-aminopyridine) isophthalic acid]. The degradation of ciprofloxacin (CIP) in water by compounds 1–4 was studied under visible light. The experimental results show that compounds 1–4 have obvious photocatalytic degradation effect on CIP. In addition, for compound 1, the effects of temperature, pH, and adsorbent dosage on photocatalytic performance were also investigated. The stability of compound 1 was observed by a cycle experiment, indicating that there was no significant change after three cycles of CIP degradation.
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spelling pubmed-96939742022-11-26 M-Carboxylic Acid Induced Formation of New Coordination Polymers for Efficient Photocatalytic Degradation of Ciprofloxacin Li, Jian Wang, Xiaojia Niu, Yunyin Molecules Article Four new 2–3D materials were designed and synthesized by hydrothermal methods, namely, {[(L1·Cu·2H(2)O) (4,4-bipy)(0.5)] (β-Mo(8)O(26))(0.5)·H(2)O} (1), {[(L1·Cu)(2)·(4,4-bipy)] (Mo(5)O(16))} (2), {Co(L1)(2)}(n) (3), and {[(L1)(2)][β-Mo(8)O(26)](0.5)·5H(2)O} (4). [L1=5-(4-aminopyridine) isophthalic acid]. The degradation of ciprofloxacin (CIP) in water by compounds 1–4 was studied under visible light. The experimental results show that compounds 1–4 have obvious photocatalytic degradation effect on CIP. In addition, for compound 1, the effects of temperature, pH, and adsorbent dosage on photocatalytic performance were also investigated. The stability of compound 1 was observed by a cycle experiment, indicating that there was no significant change after three cycles of CIP degradation. MDPI 2022-11-10 /pmc/articles/PMC9693974/ /pubmed/36431831 http://dx.doi.org/10.3390/molecules27227731 Text en © 2022 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
Li, Jian
Wang, Xiaojia
Niu, Yunyin
M-Carboxylic Acid Induced Formation of New Coordination Polymers for Efficient Photocatalytic Degradation of Ciprofloxacin
title M-Carboxylic Acid Induced Formation of New Coordination Polymers for Efficient Photocatalytic Degradation of Ciprofloxacin
title_full M-Carboxylic Acid Induced Formation of New Coordination Polymers for Efficient Photocatalytic Degradation of Ciprofloxacin
title_fullStr M-Carboxylic Acid Induced Formation of New Coordination Polymers for Efficient Photocatalytic Degradation of Ciprofloxacin
title_full_unstemmed M-Carboxylic Acid Induced Formation of New Coordination Polymers for Efficient Photocatalytic Degradation of Ciprofloxacin
title_short M-Carboxylic Acid Induced Formation of New Coordination Polymers for Efficient Photocatalytic Degradation of Ciprofloxacin
title_sort m-carboxylic acid induced formation of new coordination polymers for efficient photocatalytic degradation of ciprofloxacin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693974/
https://www.ncbi.nlm.nih.gov/pubmed/36431831
http://dx.doi.org/10.3390/molecules27227731
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