Pyrite nanoparticles derived from mine ...
Document type :
Article dans une revue scientifique: Article original
Permalink :
Title :
Pyrite nanoparticles derived from mine waste as efficient catalyst for the activation of persulfates for degradation of tetracycline
Author(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]
Journal title :
Journal of Water Process Engineering
Volume number :
40
Pages :
101808
Publication date :
2021-04
ISSN :
22147144
HAL domain(s) :
Chimie/Catalyse
English abstract : [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, ...
Show more >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.Show less >
Show more >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.Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Collections :
Research team(s) :
Matériaux pour la catalyse (MATCAT)
Submission date :
2022-03-24T09:02:36Z
2024-01-15T16:33:07Z
2024-01-15T16:33:07Z