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An experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry

RATIONALE: The type and quantity of environmentally problematic disinfection byproducts (DBPs) produced during chlorination of water depend on the natural organic matter and organic contaminants that raw water contains, and on the operational conditions of the drinking water treatment process. There...

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Autores principales: Larsen, Freja Troj, McPherson, James Neill, McKenzie, Christine Joy, Lauritsen, Frants Roager
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286867/
https://www.ncbi.nlm.nih.gov/pubmed/35733413
http://dx.doi.org/10.1002/rcm.9339
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author Larsen, Freja Troj
McPherson, James Neill
McKenzie, Christine Joy
Lauritsen, Frants Roager
author_facet Larsen, Freja Troj
McPherson, James Neill
McKenzie, Christine Joy
Lauritsen, Frants Roager
author_sort Larsen, Freja Troj
collection PubMed
description RATIONALE: The type and quantity of environmentally problematic disinfection byproducts (DBPs) produced during chlorination of water depend on the natural organic matter and organic contaminants that raw water contains, and on the operational conditions of the drinking water treatment process. There is a need for a fast and quantitative method that determines which DBPs are produced and monitors the chemical dynamics during a drinking water treatment. METHODS: A small experimental chemical reactor (50 mL) was mounted directly onto the membrane inlet interface of a membrane inlet mass spectrometer (MIMS). In this setup, the membrane was the only separation between the reaction mixture in the chemical reactor and the open ion source of the mass spectrometer 2 cm away. Water samples to be chlorinated were placed in the reactor and the chlorination reaction was initiated by injection of hypochlorite. The formation of intermediates and products was monitored using either full‐scan mass spectra or selected ion monitoring of relevant ions. RESULTS: An algorithm for analyte quantification was successfully developed for analysis of the complex mixtures of phenol (a model for waterborne organic compounds), chlorinated intermediates and trihalomethane products which simultaneously pass the membrane into the mass spectrometer. The algorithm is based upon the combined use of standard addition and an internal standard, and all analytes could be quantified at nanomolar concentrations corresponding to realistic water treatment conditions. Experiments carried out in the temperature range 15–60°C showed that the reaction dynamics change with operational parameters, for example in tap versus deionized water. CONCLUSIONS: We have successfully shown that an experimental laboratory reactor directly interfaced with a MIMS can be used for quantitative monitoring of the chemical dynamics during a water treatment. This technique could provide rapid assistance in the optimization of operating parameters for minimizing DBP production.
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spelling pubmed-92868672022-07-19 An experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry Larsen, Freja Troj McPherson, James Neill McKenzie, Christine Joy Lauritsen, Frants Roager Rapid Commun Mass Spectrom Research Articles RATIONALE: The type and quantity of environmentally problematic disinfection byproducts (DBPs) produced during chlorination of water depend on the natural organic matter and organic contaminants that raw water contains, and on the operational conditions of the drinking water treatment process. There is a need for a fast and quantitative method that determines which DBPs are produced and monitors the chemical dynamics during a drinking water treatment. METHODS: A small experimental chemical reactor (50 mL) was mounted directly onto the membrane inlet interface of a membrane inlet mass spectrometer (MIMS). In this setup, the membrane was the only separation between the reaction mixture in the chemical reactor and the open ion source of the mass spectrometer 2 cm away. Water samples to be chlorinated were placed in the reactor and the chlorination reaction was initiated by injection of hypochlorite. The formation of intermediates and products was monitored using either full‐scan mass spectra or selected ion monitoring of relevant ions. RESULTS: An algorithm for analyte quantification was successfully developed for analysis of the complex mixtures of phenol (a model for waterborne organic compounds), chlorinated intermediates and trihalomethane products which simultaneously pass the membrane into the mass spectrometer. The algorithm is based upon the combined use of standard addition and an internal standard, and all analytes could be quantified at nanomolar concentrations corresponding to realistic water treatment conditions. Experiments carried out in the temperature range 15–60°C showed that the reaction dynamics change with operational parameters, for example in tap versus deionized water. CONCLUSIONS: We have successfully shown that an experimental laboratory reactor directly interfaced with a MIMS can be used for quantitative monitoring of the chemical dynamics during a water treatment. This technique could provide rapid assistance in the optimization of operating parameters for minimizing DBP production. John Wiley and Sons Inc. 2022-07-02 2022-08-30 /pmc/articles/PMC9286867/ /pubmed/35733413 http://dx.doi.org/10.1002/rcm.9339 Text en © 2022 The Authors. Rapid Communications in Mass Spectrometry published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Larsen, Freja Troj
McPherson, James Neill
McKenzie, Christine Joy
Lauritsen, Frants Roager
An experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry
title An experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry
title_full An experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry
title_fullStr An experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry
title_full_unstemmed An experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry
title_short An experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry
title_sort experimental laboratory reactor for quantitative kinetic studies of disinfection byproduct formation using membrane inlet mass spectrometry
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286867/
https://www.ncbi.nlm.nih.gov/pubmed/35733413
http://dx.doi.org/10.1002/rcm.9339
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