Catalytic Activation of Hydrogen Peroxide Using Highly Porous Hydrothermally Modified Manganese Catalysts for Removal of Azithromycin Antibiotic from Aqueous Solution
Hydrogen peroxide catalytic activation holds great promise in the treatment of persistent pollutants. In this study, the novel Mn-Acacair/Al, Mn-Acacarg/Al and Mn-BTCarg/Al catalysts, supported on Al2O3, were applied for rapid hydrogen peroxide activation and azithromycin antibiotic removal. The cat...
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description | Hydrogen peroxide catalytic activation holds great promise in the treatment of persistent pollutants. In this study, the novel Mn-Acacair/Al, Mn-Acacarg/Al and Mn-BTCarg/Al catalysts, supported on Al2O3, were applied for rapid hydrogen peroxide activation and azithromycin antibiotic removal. The catalysts were prepared by the calcination-hydrothermal method under air or argon atmosphere. The characterization confirmed that the modification of manganese with acetylacetonate and benzene-1,3,5-tricarboxylic acid (H3BTC) O-donor ligands highly improves the catalyst porosity, amorphousity, and abundance of coordinately unsaturated sites, which facilitate the generation of reactive oxygen species. The hydrogen peroxide activation and azithromycin removal reached 98.4% and 99.3% after 40 min using the Mn-BTCarg/Al catalyst with incredible stability and reusability. Only a 5.2% decrease in activity and less than 2% manganese releasing in solutions were detected after five regeneration cycles under the optimum operating conditions. The removal intermediates were identified by LC-MS/MS analysis, and the pathways were proposed. The hydroxylation and decarboxylation reactions play a key role in the degradation reaction. |
doi_str_mv | 10.3390/catal13010077 |
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In this study, the novel Mn-Acacair/Al, Mn-Acacarg/Al and Mn-BTCarg/Al catalysts, supported on Al2O3, were applied for rapid hydrogen peroxide activation and azithromycin antibiotic removal. The catalysts were prepared by the calcination-hydrothermal method under air or argon atmosphere. The characterization confirmed that the modification of manganese with acetylacetonate and benzene-1,3,5-tricarboxylic acid (H3BTC) O-donor ligands highly improves the catalyst porosity, amorphousity, and abundance of coordinately unsaturated sites, which facilitate the generation of reactive oxygen species. The hydrogen peroxide activation and azithromycin removal reached 98.4% and 99.3% after 40 min using the Mn-BTCarg/Al catalyst with incredible stability and reusability. Only a 5.2% decrease in activity and less than 2% manganese releasing in solutions were detected after five regeneration cycles under the optimum operating conditions. The removal intermediates were identified by LC-MS/MS analysis, and the pathways were proposed. The hydroxylation and decarboxylation reactions play a key role in the degradation reaction.</description><identifier>ISSN: 2073-4344</identifier><identifier>EISSN: 2073-4344</identifier><identifier>DOI: 10.3390/catal13010077</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Alumina ; Aluminum oxide ; Antibiotics ; Aqueous solutions ; Argon ; Catalysts ; Chemical reactions ; Decarboxylation ; Efficiency ; Graphene ; Hydrocarbons ; Hydrogen peroxide ; Hydroxylation ; Investigations ; Ligands ; Manganese ; Microscopy ; Oxidation ; Pollutants ; Sodium ; Solvents ; Trimesic acid ; Water treatment</subject><ispartof>Catalysts, 2023-01, Vol.13 (1), p.77</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. 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In this study, the novel Mn-Acacair/Al, Mn-Acacarg/Al and Mn-BTCarg/Al catalysts, supported on Al2O3, were applied for rapid hydrogen peroxide activation and azithromycin antibiotic removal. The catalysts were prepared by the calcination-hydrothermal method under air or argon atmosphere. The characterization confirmed that the modification of manganese with acetylacetonate and benzene-1,3,5-tricarboxylic acid (H3BTC) O-donor ligands highly improves the catalyst porosity, amorphousity, and abundance of coordinately unsaturated sites, which facilitate the generation of reactive oxygen species. The hydrogen peroxide activation and azithromycin removal reached 98.4% and 99.3% after 40 min using the Mn-BTCarg/Al catalyst with incredible stability and reusability. Only a 5.2% decrease in activity and less than 2% manganese releasing in solutions were detected after five regeneration cycles under the optimum operating conditions. 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In this study, the novel Mn-Acacair/Al, Mn-Acacarg/Al and Mn-BTCarg/Al catalysts, supported on Al2O3, were applied for rapid hydrogen peroxide activation and azithromycin antibiotic removal. The catalysts were prepared by the calcination-hydrothermal method under air or argon atmosphere. The characterization confirmed that the modification of manganese with acetylacetonate and benzene-1,3,5-tricarboxylic acid (H3BTC) O-donor ligands highly improves the catalyst porosity, amorphousity, and abundance of coordinately unsaturated sites, which facilitate the generation of reactive oxygen species. The hydrogen peroxide activation and azithromycin removal reached 98.4% and 99.3% after 40 min using the Mn-BTCarg/Al catalyst with incredible stability and reusability. Only a 5.2% decrease in activity and less than 2% manganese releasing in solutions were detected after five regeneration cycles under the optimum operating conditions. 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subjects | Alumina Aluminum oxide Antibiotics Aqueous solutions Argon Catalysts Chemical reactions Decarboxylation Efficiency Graphene Hydrocarbons Hydrogen peroxide Hydroxylation Investigations Ligands Manganese Microscopy Oxidation Pollutants Sodium Solvents Trimesic acid Water treatment |
title | Catalytic Activation of Hydrogen Peroxide Using Highly Porous Hydrothermally Modified Manganese Catalysts for Removal of Azithromycin Antibiotic from Aqueous Solution |
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