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Ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms
Carbamazepine (CBZ) is a recalcitrant pharmaceutical often detected in wastewater and in the environment. CBZ can be removed from wastewater through advanced oxidation treatment methods such as ozonation. In this study, CBZ and its transformation product 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-di...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293669/ https://www.ncbi.nlm.nih.gov/pubmed/32333356 http://dx.doi.org/10.1007/s11356-020-08795-0 |
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author | Kråkström, Matilda Saeid, Soudabeh Tolvanen, Pasi Kumar, Narendra Salmi, Tapio Kronberg, Leif Eklund, Patrik |
author_facet | Kråkström, Matilda Saeid, Soudabeh Tolvanen, Pasi Kumar, Narendra Salmi, Tapio Kronberg, Leif Eklund, Patrik |
author_sort | Kråkström, Matilda |
collection | PubMed |
description | Carbamazepine (CBZ) is a recalcitrant pharmaceutical often detected in wastewater and in the environment. CBZ can be removed from wastewater through advanced oxidation treatment methods such as ozonation. In this study, CBZ and its transformation product 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-dione (BQD) were ozonated, and the formation and transformation of their ozonation products were investigated using liquid chromatography coupled to ion trap mass spectrometry and high-resolution mass spectrometry as well as nuclear magnetic resonance (NMR). The main products, 1-(2-benzaldehyde)-4-hydro-(1H,3H)-quinazoline-2-one (BQM) and BQD were quantified using isolated standards and LC-UV. Of the original CBZ concentration, 74% was transformed into BQM and 83% of BQM was further transformed into BQD. Both products are more stable than CBZ and could still be detected after 240 min of ozonation. Another major product, 2,2′-azanediyldibenzaldehyde (TP225) was for the first time identified using NMR. Twelve further CBZ products were identified. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11356-020-08795-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7293669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-72936692020-06-16 Ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms Kråkström, Matilda Saeid, Soudabeh Tolvanen, Pasi Kumar, Narendra Salmi, Tapio Kronberg, Leif Eklund, Patrik Environ Sci Pollut Res Int Research Article Carbamazepine (CBZ) is a recalcitrant pharmaceutical often detected in wastewater and in the environment. CBZ can be removed from wastewater through advanced oxidation treatment methods such as ozonation. In this study, CBZ and its transformation product 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-dione (BQD) were ozonated, and the formation and transformation of their ozonation products were investigated using liquid chromatography coupled to ion trap mass spectrometry and high-resolution mass spectrometry as well as nuclear magnetic resonance (NMR). The main products, 1-(2-benzaldehyde)-4-hydro-(1H,3H)-quinazoline-2-one (BQM) and BQD were quantified using isolated standards and LC-UV. Of the original CBZ concentration, 74% was transformed into BQM and 83% of BQM was further transformed into BQD. Both products are more stable than CBZ and could still be detected after 240 min of ozonation. Another major product, 2,2′-azanediyldibenzaldehyde (TP225) was for the first time identified using NMR. Twelve further CBZ products were identified. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11356-020-08795-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-04-25 2020 /pmc/articles/PMC7293669/ /pubmed/32333356 http://dx.doi.org/10.1007/s11356-020-08795-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Kråkström, Matilda Saeid, Soudabeh Tolvanen, Pasi Kumar, Narendra Salmi, Tapio Kronberg, Leif Eklund, Patrik Ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms |
title | Ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms |
title_full | Ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms |
title_fullStr | Ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms |
title_full_unstemmed | Ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms |
title_short | Ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms |
title_sort | ozonation of carbamazepine and its main transformation products: product determination and reaction mechanisms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293669/ https://www.ncbi.nlm.nih.gov/pubmed/32333356 http://dx.doi.org/10.1007/s11356-020-08795-0 |
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