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Hybrid Biochar/Ceria Nanomaterials: Synthesis, Characterization and Activity Assessment for the Persulfate-Induced Degradation of Antibiotic Sulfamethoxazole

Biochar from spent malt rootlets was employed as the template to synthesize hybrid biochar-ceria materials through a wet impregnation method. The materials were tested for the activation of persulfate (SPS) and subsequent degradation of sulfamethoxazole (SMX), a representative antibiotic, in various...

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Autores principales: Papatheodorou, Golfo, Ntzoufra, Paraskevi, Hapeshi, Evroula, Vakros, John, Mantzavinos, Dionissios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778396/
https://www.ncbi.nlm.nih.gov/pubmed/35055213
http://dx.doi.org/10.3390/nano12020194
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author Papatheodorou, Golfo
Ntzoufra, Paraskevi
Hapeshi, Evroula
Vakros, John
Mantzavinos, Dionissios
author_facet Papatheodorou, Golfo
Ntzoufra, Paraskevi
Hapeshi, Evroula
Vakros, John
Mantzavinos, Dionissios
author_sort Papatheodorou, Golfo
collection PubMed
description Biochar from spent malt rootlets was employed as the template to synthesize hybrid biochar-ceria materials through a wet impregnation method. The materials were tested for the activation of persulfate (SPS) and subsequent degradation of sulfamethoxazole (SMX), a representative antibiotic, in various matrices. Different calcination temperatures in the range 300–500 °C were employed and the resulting materials were characterized by means of N(2) adsorption and potentiometric mass titration as well as TGA, XRD, SEM, FTIR, DRS, and Raman spectroscopy. Calcination temperature affects the biochar content and the physicochemical properties of the hybrid materials, which were tested for the degradation of 500 μg L(−1) SMX with SPS (in the range 200–500 mg L(−1)) in various matrices including ultrapure water (UPW), bottled water, wastewater, and UPW spiked with bicarbonate, chloride, or humic acid. Materials calcined at 300–350 °C, with a surface area of ca. 120 m(2) g(−1), were the most active, yielding ca. 65% SMX degradation after 120 min of reaction in UPW; materials calcined at higher temperatures as well as bare biochar were less active. Degradation decreased with increasing matrix complexity due to the interactions amongst the surface, the contaminant, and the oxidant. Experiments in the presence of scavengers (i.e., methanol, t-butanol, and sodium azide) revealed that sulfate and hydroxyl radicals as well as singlet oxygen were the main oxidative species.
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spelling pubmed-87783962022-01-22 Hybrid Biochar/Ceria Nanomaterials: Synthesis, Characterization and Activity Assessment for the Persulfate-Induced Degradation of Antibiotic Sulfamethoxazole Papatheodorou, Golfo Ntzoufra, Paraskevi Hapeshi, Evroula Vakros, John Mantzavinos, Dionissios Nanomaterials (Basel) Article Biochar from spent malt rootlets was employed as the template to synthesize hybrid biochar-ceria materials through a wet impregnation method. The materials were tested for the activation of persulfate (SPS) and subsequent degradation of sulfamethoxazole (SMX), a representative antibiotic, in various matrices. Different calcination temperatures in the range 300–500 °C were employed and the resulting materials were characterized by means of N(2) adsorption and potentiometric mass titration as well as TGA, XRD, SEM, FTIR, DRS, and Raman spectroscopy. Calcination temperature affects the biochar content and the physicochemical properties of the hybrid materials, which were tested for the degradation of 500 μg L(−1) SMX with SPS (in the range 200–500 mg L(−1)) in various matrices including ultrapure water (UPW), bottled water, wastewater, and UPW spiked with bicarbonate, chloride, or humic acid. Materials calcined at 300–350 °C, with a surface area of ca. 120 m(2) g(−1), were the most active, yielding ca. 65% SMX degradation after 120 min of reaction in UPW; materials calcined at higher temperatures as well as bare biochar were less active. Degradation decreased with increasing matrix complexity due to the interactions amongst the surface, the contaminant, and the oxidant. Experiments in the presence of scavengers (i.e., methanol, t-butanol, and sodium azide) revealed that sulfate and hydroxyl radicals as well as singlet oxygen were the main oxidative species. MDPI 2022-01-07 /pmc/articles/PMC8778396/ /pubmed/35055213 http://dx.doi.org/10.3390/nano12020194 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Papatheodorou, Golfo
Ntzoufra, Paraskevi
Hapeshi, Evroula
Vakros, John
Mantzavinos, Dionissios
Hybrid Biochar/Ceria Nanomaterials: Synthesis, Characterization and Activity Assessment for the Persulfate-Induced Degradation of Antibiotic Sulfamethoxazole
title Hybrid Biochar/Ceria Nanomaterials: Synthesis, Characterization and Activity Assessment for the Persulfate-Induced Degradation of Antibiotic Sulfamethoxazole
title_full Hybrid Biochar/Ceria Nanomaterials: Synthesis, Characterization and Activity Assessment for the Persulfate-Induced Degradation of Antibiotic Sulfamethoxazole
title_fullStr Hybrid Biochar/Ceria Nanomaterials: Synthesis, Characterization and Activity Assessment for the Persulfate-Induced Degradation of Antibiotic Sulfamethoxazole
title_full_unstemmed Hybrid Biochar/Ceria Nanomaterials: Synthesis, Characterization and Activity Assessment for the Persulfate-Induced Degradation of Antibiotic Sulfamethoxazole
title_short Hybrid Biochar/Ceria Nanomaterials: Synthesis, Characterization and Activity Assessment for the Persulfate-Induced Degradation of Antibiotic Sulfamethoxazole
title_sort hybrid biochar/ceria nanomaterials: synthesis, characterization and activity assessment for the persulfate-induced degradation of antibiotic sulfamethoxazole
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778396/
https://www.ncbi.nlm.nih.gov/pubmed/35055213
http://dx.doi.org/10.3390/nano12020194
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