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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-9092016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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