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Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis
The effective and efficient degradation of persistent, recalcitrant pollutants by advanced oxidation processes is vital to both reduce hazardous waste and remediate polluted waters. One such advanced oxidation process is the use of Fenton chemistry, which can be optimized using heterogeneous catalys...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103896/ https://www.ncbi.nlm.nih.gov/pubmed/37067880 |
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author | Compton, P Dehkordi, NR Larese Casanova, P Alshawabkeh, AN |
author_facet | Compton, P Dehkordi, NR Larese Casanova, P Alshawabkeh, AN |
author_sort | Compton, P |
collection | PubMed |
description | The effective and efficient degradation of persistent, recalcitrant pollutants by advanced oxidation processes is vital to both reduce hazardous waste and remediate polluted waters. One such advanced oxidation process is the use of Fenton chemistry, which can be optimized using heterogeneous catalysts. However, to make this AOP viable over conventional treatment methods, the technology needs to be optimized from both a technical and economic standpoint. From a heterogeneous catalyst optimization perspective, varying the surface chemistry of activated carbon and impregnating or doping with Fenton-like catalytic nanomaterials removes precipitation complications associated with traditional iron species in Fenton chemistry while generating effective amounts of highly oxidative hydroxyl radicals. Utilizing various techniques to synthesize heterogeneous catalysts with activated carbon as a backbone, in the presence of H(2)O(2) the formation of hydroxyl radicals and removal of benzoic acid is tested. Comparing various additives, raw activated carbon impregnated with 5% MnO(2) in the presence of H(2)O(2) realized a high concentration of hydroxyl radical formation while maintaining low cost and relative ease of synthesis. This AC-Mn5 catalyst performed effectively in varying concentrations of H(2)O(2), utilizing various synthesis techniques, after simulated aging of the catalyst structure, and over a wide pH range with the highest radical formation at acidic pH values. Utilizing this catalytic material as a substitute for iron species associated with traditional Fenton technology, the goal of designing a full set of oxidation functions towards persistent, recalcitrant pollutant removal while maintaining cost-effectiveness and scalability is proposed. It is anticipated these catalytic materials are effective to eliminate analogous contaminants and mixtures. |
format | Online Article Text |
id | pubmed-10103896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-101038962023-04-14 Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis Compton, P Dehkordi, NR Larese Casanova, P Alshawabkeh, AN J Chem Eng Catal Article The effective and efficient degradation of persistent, recalcitrant pollutants by advanced oxidation processes is vital to both reduce hazardous waste and remediate polluted waters. One such advanced oxidation process is the use of Fenton chemistry, which can be optimized using heterogeneous catalysts. However, to make this AOP viable over conventional treatment methods, the technology needs to be optimized from both a technical and economic standpoint. From a heterogeneous catalyst optimization perspective, varying the surface chemistry of activated carbon and impregnating or doping with Fenton-like catalytic nanomaterials removes precipitation complications associated with traditional iron species in Fenton chemistry while generating effective amounts of highly oxidative hydroxyl radicals. Utilizing various techniques to synthesize heterogeneous catalysts with activated carbon as a backbone, in the presence of H(2)O(2) the formation of hydroxyl radicals and removal of benzoic acid is tested. Comparing various additives, raw activated carbon impregnated with 5% MnO(2) in the presence of H(2)O(2) realized a high concentration of hydroxyl radical formation while maintaining low cost and relative ease of synthesis. This AC-Mn5 catalyst performed effectively in varying concentrations of H(2)O(2), utilizing various synthesis techniques, after simulated aging of the catalyst structure, and over a wide pH range with the highest radical formation at acidic pH values. Utilizing this catalytic material as a substitute for iron species associated with traditional Fenton technology, the goal of designing a full set of oxidation functions towards persistent, recalcitrant pollutant removal while maintaining cost-effectiveness and scalability is proposed. It is anticipated these catalytic materials are effective to eliminate analogous contaminants and mixtures. 2022 2022-06-10 /pmc/articles/PMC10103896/ /pubmed/37067880 Text en https://creativecommons.org/licenses/by/3.0/The Authors. Published by the JScholar under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Article Compton, P Dehkordi, NR Larese Casanova, P Alshawabkeh, AN Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis |
title | Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis |
title_full | Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis |
title_fullStr | Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis |
title_full_unstemmed | Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis |
title_short | Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis |
title_sort | activated carbon modifications for heterogeneous fenton-like catalysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103896/ https://www.ncbi.nlm.nih.gov/pubmed/37067880 |
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