Pyrite nanoparticles derived from mine ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Pyrite nanoparticles derived from mine waste as efficient catalyst for the activation of persulfates for degradation of tetracycline
Auteur(s) :
Rahimi, Farzaneh [Auteur]
van der Hoek, Jan Peter [Auteur]
Delft University of Technology [TU Delft]
royer, sebastien [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Javid, Allahbakhsh [Auteur]
Mashayekh-Salehi, Ali [Auteur]
Jafari Sani, Moslem [Auteur]
van der Hoek, Jan Peter [Auteur]
Delft University of Technology [TU Delft]
royer, sebastien [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Javid, Allahbakhsh [Auteur]
Mashayekh-Salehi, Ali [Auteur]
Jafari Sani, Moslem [Auteur]
Titre de la revue :
Journal of Water Process Engineering
Numéro :
40
Pagination :
101808
Date de publication :
2021-04
ISSN :
22147144
Discipline(s) HAL :
Chimie/Catalyse
Résumé en anglais : [en]
Pyrite mine waste was used as a non-toxic and natural catalyst for the activation of peroxydisulfate (PDS) and peroxymonosulfate (PMS) to oxidize tetracycline (TTC), one of the most extensively used antibiotics worldwide, ...
Lire la suite >Pyrite mine waste was used as a non-toxic and natural catalyst for the activation of peroxydisulfate (PDS) and peroxymonosulfate (PMS) to oxidize tetracycline (TTC), one of the most extensively used antibiotics worldwide, in contaminated water. The results demonstrated that PMS was activated more effectively than PDS by using pyrite. Scavenging experiments indicated that both OHradical dot and SO4radical dot− were the main oxidative species in the pyrite/PMS process, while SO4radical dot− was more dominant. A high degradation of 98.3 % and significant mineralization (up to 46 %) of TTC (50 mg/L) were achieved using pyrite activated PMS at a reaction time of 30 and 60 min, respectively. In-vivo toxicity of raw and pyrite/PMS treated TTC solutions was evaluated using biochemical and histopathological assays. The results revealed that the pyrite/PMS process significantly decreased the nephrotoxicity (90 %) and hepatotoxicity (85 %) effect of TTC. Catalyst reusability was evaluated under cycling conditions. No significant decrease in process efficiency was measured between the first and fourth cycle (<3% decrease in TTC removal). In conclusion, mine waste pyrite nanoparticles can be considered as a non-toxic and clean catalyst to activate PMS for an effective detoxification, degradation, and intermediate mineralization of TTC, as a refractory water pollutant.Lire moins >
Lire la suite >Pyrite mine waste was used as a non-toxic and natural catalyst for the activation of peroxydisulfate (PDS) and peroxymonosulfate (PMS) to oxidize tetracycline (TTC), one of the most extensively used antibiotics worldwide, in contaminated water. The results demonstrated that PMS was activated more effectively than PDS by using pyrite. Scavenging experiments indicated that both OHradical dot and SO4radical dot− were the main oxidative species in the pyrite/PMS process, while SO4radical dot− was more dominant. A high degradation of 98.3 % and significant mineralization (up to 46 %) of TTC (50 mg/L) were achieved using pyrite activated PMS at a reaction time of 30 and 60 min, respectively. In-vivo toxicity of raw and pyrite/PMS treated TTC solutions was evaluated using biochemical and histopathological assays. The results revealed that the pyrite/PMS process significantly decreased the nephrotoxicity (90 %) and hepatotoxicity (85 %) effect of TTC. Catalyst reusability was evaluated under cycling conditions. No significant decrease in process efficiency was measured between the first and fourth cycle (<3% decrease in TTC removal). In conclusion, mine waste pyrite nanoparticles can be considered as a non-toxic and clean catalyst to activate PMS for an effective detoxification, degradation, and intermediate mineralization of TTC, as a refractory water pollutant.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Collections :
Équipe(s) de recherche :
Matériaux pour la catalyse (MATCAT)
Date de dépôt :
2022-03-24T09:02:36Z
2024-01-15T16:33:07Z
2024-01-15T16:33:07Z