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Peroxymonosulfate activation by tea residue biochar loaded with Fe(3)O(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism

The recycling of agricultural and food waste is an effective way to reduce resource waste and ameliorate the shortage of natural resources. The treatment of antibiotic wastewater is a current research hotspot. In this study, waste tea residue was used as a raw material to prepare biochar (T-BC) and...

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Autores principales: Wang, Qirui, Shi, Yixuan, Lv, Shiyi, Liang, Ying, Xiao, Pengfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033424/
https://www.ncbi.nlm.nih.gov/pubmed/35480906
http://dx.doi.org/10.1039/d1ra01640g
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author Wang, Qirui
Shi, Yixuan
Lv, Shiyi
Liang, Ying
Xiao, Pengfei
author_facet Wang, Qirui
Shi, Yixuan
Lv, Shiyi
Liang, Ying
Xiao, Pengfei
author_sort Wang, Qirui
collection PubMed
description The recycling of agricultural and food waste is an effective way to reduce resource waste and ameliorate the shortage of natural resources. The treatment of antibiotic wastewater is a current research hotspot. In this study, waste tea residue was used as a raw material to prepare biochar (T-BC) and loaded with Fe(3)O(4) as a catalyst to activate peroxymonosulfate (PMS) for oxidative degradation of tetracycline hydrochloride (TCH). Analysis techniques such as BET, SEM, XRD, FT-IR, XPS and VSM indicated that the heterogeneous catalyst (Fe(3)O(4)@T-BC) with good surface properties and magnetic properties was successfully prepared. The results of batch-scale experiments illustrated that when the dose of the Fe(3)O(4)@T-BC catalyst was 1 g L(−1), the concentration of PMS was 1 g L(−1), and the initial pH was 7, the degradation rate of TCH with a concentration of 50 mg L(−1) reached 97.89% after 60 minutes of reaction. When the initial pH was 11, the degradation rate of TCH reached 99.86%. After the catalyst was recycled four times using an external magnet, the degradation rate of TCH could still reach 71.32%. The data of removal of TCH could be best fitted by a pseudo-first-order model. The analysis of the degradation mechanism through a free radical quenching experiment and EPR analysis, as well as the exploration of TCH intermediate products and reaction paths through the LC-MS method, all confirmed that the Fe(3)O(4)@T-BC prepared by this method is expected to become a cost-effective and environmentally friendly heterogeneous catalyst for activating persulfate degradation of tetracycline antibiotics.
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spelling pubmed-90334242022-04-26 Peroxymonosulfate activation by tea residue biochar loaded with Fe(3)O(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism Wang, Qirui Shi, Yixuan Lv, Shiyi Liang, Ying Xiao, Pengfei RSC Adv Chemistry The recycling of agricultural and food waste is an effective way to reduce resource waste and ameliorate the shortage of natural resources. The treatment of antibiotic wastewater is a current research hotspot. In this study, waste tea residue was used as a raw material to prepare biochar (T-BC) and loaded with Fe(3)O(4) as a catalyst to activate peroxymonosulfate (PMS) for oxidative degradation of tetracycline hydrochloride (TCH). Analysis techniques such as BET, SEM, XRD, FT-IR, XPS and VSM indicated that the heterogeneous catalyst (Fe(3)O(4)@T-BC) with good surface properties and magnetic properties was successfully prepared. The results of batch-scale experiments illustrated that when the dose of the Fe(3)O(4)@T-BC catalyst was 1 g L(−1), the concentration of PMS was 1 g L(−1), and the initial pH was 7, the degradation rate of TCH with a concentration of 50 mg L(−1) reached 97.89% after 60 minutes of reaction. When the initial pH was 11, the degradation rate of TCH reached 99.86%. After the catalyst was recycled four times using an external magnet, the degradation rate of TCH could still reach 71.32%. The data of removal of TCH could be best fitted by a pseudo-first-order model. The analysis of the degradation mechanism through a free radical quenching experiment and EPR analysis, as well as the exploration of TCH intermediate products and reaction paths through the LC-MS method, all confirmed that the Fe(3)O(4)@T-BC prepared by this method is expected to become a cost-effective and environmentally friendly heterogeneous catalyst for activating persulfate degradation of tetracycline antibiotics. The Royal Society of Chemistry 2021-05-22 /pmc/articles/PMC9033424/ /pubmed/35480906 http://dx.doi.org/10.1039/d1ra01640g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Qirui
Shi, Yixuan
Lv, Shiyi
Liang, Ying
Xiao, Pengfei
Peroxymonosulfate activation by tea residue biochar loaded with Fe(3)O(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism
title Peroxymonosulfate activation by tea residue biochar loaded with Fe(3)O(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism
title_full Peroxymonosulfate activation by tea residue biochar loaded with Fe(3)O(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism
title_fullStr Peroxymonosulfate activation by tea residue biochar loaded with Fe(3)O(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism
title_full_unstemmed Peroxymonosulfate activation by tea residue biochar loaded with Fe(3)O(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism
title_short Peroxymonosulfate activation by tea residue biochar loaded with Fe(3)O(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism
title_sort peroxymonosulfate activation by tea residue biochar loaded with fe(3)o(4) for the degradation of tetracycline hydrochloride: performance and reaction mechanism
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033424/
https://www.ncbi.nlm.nih.gov/pubmed/35480906
http://dx.doi.org/10.1039/d1ra01640g
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