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Study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported Co(3)O(4)

Tetracycline hydrochloride (TCH) degradation by cobalt modified silicate ore (CoSO) catalytic ozonation in aqueous solution was investigated. CoSO catalyst was synthesized by an impregnation method using Co(NO(3))(2) as the precursor and natural silicon ore (SO) as the support. The key catalyst prep...

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Autores principales: Luo, Lisha, Zou, Donglei, Lu, Dongwei, Yu, Fengli, Xin, Bingjing, Ma, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092016/
https://www.ncbi.nlm.nih.gov/pubmed/35559322
http://dx.doi.org/10.1039/c8ra08402e
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author Luo, Lisha
Zou, Donglei
Lu, Dongwei
Yu, Fengli
Xin, Bingjing
Ma, Jun
author_facet Luo, Lisha
Zou, Donglei
Lu, Dongwei
Yu, Fengli
Xin, Bingjing
Ma, Jun
author_sort Luo, Lisha
collection PubMed
description Tetracycline hydrochloride (TCH) degradation by cobalt modified silicate ore (CoSO) catalytic ozonation in aqueous solution was investigated. CoSO catalyst was synthesized by an impregnation method using Co(NO(3))(2) as the precursor and natural silicon ore (SO) as the support. The key catalyst preparation conditions (i.e., impregnation concentration, calcination temperature and time) were optimized. The activity and stability of CoSO catalyst and its catalytic ozonation mechanism for TCH degradation were studied. The results showed that Co(3)O(4) was successfully coated on the silicon ore and the CoSO catalyst was highly efficient in catalytic ozonation for TCH degradation. The TCH removal by CoSO/O(3) could reach 93.2%, while only 69.3% by SO/O(3) and only 46.0% by O(3) alone at 25 min. The reaction of TCH degradation followed pseudo-first order kinetics. TOC removal rate by CoSO/O(3) was 2.0 times higher than that by SO/O(3), and 3.5 times higher than that by O(3) alone. The reaction conditions (TCH initial concentration, catalyst concentration, pH and temperature) for catalytic ozonation were systematically investigated. The possible mechanism for the CoSO catalytic ozonation process was proposed, where hydroxyl radical oxidation mainly accounted for the substantial TCH degradation. Furthermore, CoSO showed great durability and stability after seven reaction cycles.
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spelling pubmed-90920162022-05-11 Study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported Co(3)O(4) Luo, Lisha Zou, Donglei Lu, Dongwei Yu, Fengli Xin, Bingjing Ma, Jun RSC Adv Chemistry Tetracycline hydrochloride (TCH) degradation by cobalt modified silicate ore (CoSO) catalytic ozonation in aqueous solution was investigated. CoSO catalyst was synthesized by an impregnation method using Co(NO(3))(2) as the precursor and natural silicon ore (SO) as the support. The key catalyst preparation conditions (i.e., impregnation concentration, calcination temperature and time) were optimized. The activity and stability of CoSO catalyst and its catalytic ozonation mechanism for TCH degradation were studied. The results showed that Co(3)O(4) was successfully coated on the silicon ore and the CoSO catalyst was highly efficient in catalytic ozonation for TCH degradation. The TCH removal by CoSO/O(3) could reach 93.2%, while only 69.3% by SO/O(3) and only 46.0% by O(3) alone at 25 min. The reaction of TCH degradation followed pseudo-first order kinetics. TOC removal rate by CoSO/O(3) was 2.0 times higher than that by SO/O(3), and 3.5 times higher than that by O(3) alone. The reaction conditions (TCH initial concentration, catalyst concentration, pH and temperature) for catalytic ozonation were systematically investigated. The possible mechanism for the CoSO catalytic ozonation process was proposed, where hydroxyl radical oxidation mainly accounted for the substantial TCH degradation. Furthermore, CoSO showed great durability and stability after seven reaction cycles. The Royal Society of Chemistry 2018-12-07 /pmc/articles/PMC9092016/ /pubmed/35559322 http://dx.doi.org/10.1039/c8ra08402e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Luo, Lisha
Zou, Donglei
Lu, Dongwei
Yu, Fengli
Xin, Bingjing
Ma, Jun
Study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported Co(3)O(4)
title Study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported Co(3)O(4)
title_full Study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported Co(3)O(4)
title_fullStr Study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported Co(3)O(4)
title_full_unstemmed Study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported Co(3)O(4)
title_short Study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported Co(3)O(4)
title_sort study of catalytic ozonation for tetracycline hydrochloride degradation in water by silicate ore supported co(3)o(4)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092016/
https://www.ncbi.nlm.nih.gov/pubmed/35559322
http://dx.doi.org/10.1039/c8ra08402e
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