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Generation of hydroxyl radicals from reactions between a dimethoxyhydroquinone and iron oxide nanoparticles

The hydroxyl radical (·OH) is a powerful oxidant that is produced in a wide range of environments via the Fenton reaction (Fe(2+)  + H(2)O(2) → Fe(3+)  + ·OH + OH(-)). The reactants are formed from the reduction of Fe(3+) and O(2), which may be promoted by organic reductants, such as hydroquinones....

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Detalles Bibliográficos
Autores principales: Lyngsie, Gry, Krumina, Lelde, Tunlid, Anders, Persson, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050337/
https://www.ncbi.nlm.nih.gov/pubmed/30018415
http://dx.doi.org/10.1038/s41598-018-29075-5
Descripción
Sumario:The hydroxyl radical (·OH) is a powerful oxidant that is produced in a wide range of environments via the Fenton reaction (Fe(2+)  + H(2)O(2) → Fe(3+)  + ·OH + OH(-)). The reactants are formed from the reduction of Fe(3+) and O(2), which may be promoted by organic reductants, such as hydroquinones. The aim of this study was to investigate the extent of ·OH formation in reactions between 2,6-dimethoxyhydroquinone (2,6-DMHQ) and iron oxide nanoparticles. We further compared the reactivities of ferrihydrite and goethite and investigated the effects of the O(2) concentration and pH on the generation of ·OH. The main finding was that the reactions between 2,6-DMHQ and iron oxide nanoparticles generated substantial amounts of ·OH under certain conditions via parallel reductive dissolution and catalytic oxidation reactions. The presence of O(2) was essential for the catalytic oxidation of 2,6-DMHQ and the generation of H(2)O(2). Moreover, the higher reduction potential of ferrihydrite relative to that of goethite made the former species more susceptible to reductive dissolution, which favored the production of ·OH. The results highlighted the effects of surface charge and ligand competition on the 2,6-DMHQ oxidation processes and showed that the co-adsorption of anions can promote the generation of ·OH.