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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...

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Autores principales: Kråkström, Matilda, Saeid, Soudabeh, Tolvanen, Pasi, Kumar, Narendra, Salmi, Tapio, Kronberg, Leif, Eklund, Patrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
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.
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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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