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Simple Urea Immersion Enhanced Removal of Tetracycline from Water by Polystyrene Microspheres

Antibiotics pose potential ecological risks in the water environment, necessitating their effective removal by reliable technologies. Adsorption is a conventional process to remove such chemicals from water without byproducts. However, finding cheap adsorbents with satisfactory performance is still...

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Detalles Bibliográficos
Autores principales: Ma, Junjun, Li, Bing, Zhou, Lincheng, Zhu, Yin, Li, Ji, Qiu, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068535/
https://www.ncbi.nlm.nih.gov/pubmed/30029466
http://dx.doi.org/10.3390/ijerph15071524
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author Ma, Junjun
Li, Bing
Zhou, Lincheng
Zhu, Yin
Li, Ji
Qiu, Yong
author_facet Ma, Junjun
Li, Bing
Zhou, Lincheng
Zhu, Yin
Li, Ji
Qiu, Yong
author_sort Ma, Junjun
collection PubMed
description Antibiotics pose potential ecological risks in the water environment, necessitating their effective removal by reliable technologies. Adsorption is a conventional process to remove such chemicals from water without byproducts. However, finding cheap adsorbents with satisfactory performance is still a challenge. In this study, polystyrene microspheres (PSM) were enhanced to adsorb tetracycline by surface modification. Simple urea immersion was used to prepare urea-immersed PSM (UPSM), of which surface groups were characterized by instruments to confirm the effect of immersion. Tetracycline hydrochloride (TC) and doxycycline (DC) were used as typical adsorbates. The adsorptive isotherms were interpreted by Langmuir, Freundlich, and Tempkin models. After urea immersion, the maximum adsorption capacity of UPSM at 293 K and pH 6.8 increased about 30% and 60%, achieving 460 mg/g for TC and 430 mg/g for DC. The kinetic data were fitted by first-order and second-order kinetics and Weber–Morris models. The first-order rate constant for TC adsorption on UPSM was 0.41 /h, and for DC was 0.33 /h. The cyclic urea immersion enabled multilayer adsorption, which increased the adsorption capacities of TC on UPSM by two to three times. The adsorption mechanism was possibly determined by the molecular interaction including π–π forces, cation-π bonding, and hydrogen bonding. The simple surface modification was helpful in enhancing the removal of antibiotics from wastewater with similar structures.
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spelling pubmed-60685352018-08-07 Simple Urea Immersion Enhanced Removal of Tetracycline from Water by Polystyrene Microspheres Ma, Junjun Li, Bing Zhou, Lincheng Zhu, Yin Li, Ji Qiu, Yong Int J Environ Res Public Health Article Antibiotics pose potential ecological risks in the water environment, necessitating their effective removal by reliable technologies. Adsorption is a conventional process to remove such chemicals from water without byproducts. However, finding cheap adsorbents with satisfactory performance is still a challenge. In this study, polystyrene microspheres (PSM) were enhanced to adsorb tetracycline by surface modification. Simple urea immersion was used to prepare urea-immersed PSM (UPSM), of which surface groups were characterized by instruments to confirm the effect of immersion. Tetracycline hydrochloride (TC) and doxycycline (DC) were used as typical adsorbates. The adsorptive isotherms were interpreted by Langmuir, Freundlich, and Tempkin models. After urea immersion, the maximum adsorption capacity of UPSM at 293 K and pH 6.8 increased about 30% and 60%, achieving 460 mg/g for TC and 430 mg/g for DC. The kinetic data were fitted by first-order and second-order kinetics and Weber–Morris models. The first-order rate constant for TC adsorption on UPSM was 0.41 /h, and for DC was 0.33 /h. The cyclic urea immersion enabled multilayer adsorption, which increased the adsorption capacities of TC on UPSM by two to three times. The adsorption mechanism was possibly determined by the molecular interaction including π–π forces, cation-π bonding, and hydrogen bonding. The simple surface modification was helpful in enhancing the removal of antibiotics from wastewater with similar structures. MDPI 2018-07-19 2018-07 /pmc/articles/PMC6068535/ /pubmed/30029466 http://dx.doi.org/10.3390/ijerph15071524 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ma, Junjun
Li, Bing
Zhou, Lincheng
Zhu, Yin
Li, Ji
Qiu, Yong
Simple Urea Immersion Enhanced Removal of Tetracycline from Water by Polystyrene Microspheres
title Simple Urea Immersion Enhanced Removal of Tetracycline from Water by Polystyrene Microspheres
title_full Simple Urea Immersion Enhanced Removal of Tetracycline from Water by Polystyrene Microspheres
title_fullStr Simple Urea Immersion Enhanced Removal of Tetracycline from Water by Polystyrene Microspheres
title_full_unstemmed Simple Urea Immersion Enhanced Removal of Tetracycline from Water by Polystyrene Microspheres
title_short Simple Urea Immersion Enhanced Removal of Tetracycline from Water by Polystyrene Microspheres
title_sort simple urea immersion enhanced removal of tetracycline from water by polystyrene microspheres
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068535/
https://www.ncbi.nlm.nih.gov/pubmed/30029466
http://dx.doi.org/10.3390/ijerph15071524
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