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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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. |
format | Online Article Text |
id | pubmed-6068535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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