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Effect of Solution pH on the Dual Role of Dissolved Organic Matter in Sensitized Pollutant Photooxidation
[Image: see text] Dissolved organic matter (DOM) has a dual role in indirect phototransformations of aquatic contaminants by acting both as a photosensitizer and an inhibitor. Herein, the pH dependence of the inhibitory effect of DOM and the underlying mechanisms were studied in more than 400 kineti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8735754/ https://www.ncbi.nlm.nih.gov/pubmed/34714642 http://dx.doi.org/10.1021/acs.est.1c03301 |
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author | Wenk, Jannis Graf, Cornelia Aeschbacher, Michael Sander, Michael Canonica, Silvio |
author_facet | Wenk, Jannis Graf, Cornelia Aeschbacher, Michael Sander, Michael Canonica, Silvio |
author_sort | Wenk, Jannis |
collection | PubMed |
description | [Image: see text] Dissolved organic matter (DOM) has a dual role in indirect phototransformations of aquatic contaminants by acting both as a photosensitizer and an inhibitor. Herein, the pH dependence of the inhibitory effect of DOM and the underlying mechanisms were studied in more than 400 kinetic irradiation experiments over the pH range of 6–11. Experiments employed various combinations of one of three DOM isolates, one of two model photosensitizers, the model antioxidant phenol, and one of nine target compounds (TCs), comprising several aromatic amines, in particular anilines and sulfonamides, and 4-cyanophenol. Using model photosensitizers without antioxidants, the phototransformation of most TCs increased with increasing pH, even for TCs for which pH did not affect speciation. This trend was attributed to pH-dependent formation yields of TC-derived radicals and their re-formation to the parent TC. Analogous trends were observed with DOM as a photosensitizer. Comparison of model and DOM photosensitizer data sets showed increasing inhibitory effects of DOM on TC phototransformation kinetics with increasing pH. In systems with anilines as a TC and phenol as a model antioxidant, pH trends of the inhibitory effect could be rationalized based on the reduction potential difference (ΔE(red)) of phenoxyl/phenol and anilinyl/aniline couples. Our results indicate that the light-induced transformation of aromatic amines in the aquatic environment is governed by the pH-dependent inhibitory effects of antioxidant phenolic moieties of DOM and pH-dependent processes related to the formation of amine oxidation intermediates. |
format | Online Article Text |
id | pubmed-8735754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-87357542022-01-10 Effect of Solution pH on the Dual Role of Dissolved Organic Matter in Sensitized Pollutant Photooxidation Wenk, Jannis Graf, Cornelia Aeschbacher, Michael Sander, Michael Canonica, Silvio Environ Sci Technol [Image: see text] Dissolved organic matter (DOM) has a dual role in indirect phototransformations of aquatic contaminants by acting both as a photosensitizer and an inhibitor. Herein, the pH dependence of the inhibitory effect of DOM and the underlying mechanisms were studied in more than 400 kinetic irradiation experiments over the pH range of 6–11. Experiments employed various combinations of one of three DOM isolates, one of two model photosensitizers, the model antioxidant phenol, and one of nine target compounds (TCs), comprising several aromatic amines, in particular anilines and sulfonamides, and 4-cyanophenol. Using model photosensitizers without antioxidants, the phototransformation of most TCs increased with increasing pH, even for TCs for which pH did not affect speciation. This trend was attributed to pH-dependent formation yields of TC-derived radicals and their re-formation to the parent TC. Analogous trends were observed with DOM as a photosensitizer. Comparison of model and DOM photosensitizer data sets showed increasing inhibitory effects of DOM on TC phototransformation kinetics with increasing pH. In systems with anilines as a TC and phenol as a model antioxidant, pH trends of the inhibitory effect could be rationalized based on the reduction potential difference (ΔE(red)) of phenoxyl/phenol and anilinyl/aniline couples. Our results indicate that the light-induced transformation of aromatic amines in the aquatic environment is governed by the pH-dependent inhibitory effects of antioxidant phenolic moieties of DOM and pH-dependent processes related to the formation of amine oxidation intermediates. American Chemical Society 2021-10-29 2021-11-16 /pmc/articles/PMC8735754/ /pubmed/34714642 http://dx.doi.org/10.1021/acs.est.1c03301 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Wenk, Jannis Graf, Cornelia Aeschbacher, Michael Sander, Michael Canonica, Silvio Effect of Solution pH on the Dual Role of Dissolved Organic Matter in Sensitized Pollutant Photooxidation |
title | Effect
of Solution pH on the Dual Role of Dissolved
Organic Matter in Sensitized Pollutant Photooxidation |
title_full | Effect
of Solution pH on the Dual Role of Dissolved
Organic Matter in Sensitized Pollutant Photooxidation |
title_fullStr | Effect
of Solution pH on the Dual Role of Dissolved
Organic Matter in Sensitized Pollutant Photooxidation |
title_full_unstemmed | Effect
of Solution pH on the Dual Role of Dissolved
Organic Matter in Sensitized Pollutant Photooxidation |
title_short | Effect
of Solution pH on the Dual Role of Dissolved
Organic Matter in Sensitized Pollutant Photooxidation |
title_sort | effect
of solution ph on the dual role of dissolved
organic matter in sensitized pollutant photooxidation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8735754/ https://www.ncbi.nlm.nih.gov/pubmed/34714642 http://dx.doi.org/10.1021/acs.est.1c03301 |
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