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Determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger
Free available chlorine (FAC) is the most widely used chemical for disinfection and in secondary disinfection; a minimum chlorine residual must be present in the distribution system. FAC can also be formed as an impurity in ClO(2) production as well as a secondary oxidant in the ClO(2) application,...
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/PMC7550385/ https://www.ncbi.nlm.nih.gov/pubmed/32944811 http://dx.doi.org/10.1007/s00216-020-02885-1 |
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author | Abdighahroudi, Mohammad Sajjad Schmidt, Torsten C. Lutze, Holger V. |
author_facet | Abdighahroudi, Mohammad Sajjad Schmidt, Torsten C. Lutze, Holger V. |
author_sort | Abdighahroudi, Mohammad Sajjad |
collection | PubMed |
description | Free available chlorine (FAC) is the most widely used chemical for disinfection and in secondary disinfection; a minimum chlorine residual must be present in the distribution system. FAC can also be formed as an impurity in ClO(2) production as well as a secondary oxidant in the ClO(2) application, which has to be monitored. In this study, a new method is developed based on the reaction of FAC with glycine in which the amine group selectively scavenges FAC and the N-chloroglycine formed can be measured by ion chromatography with conductivity detector (IC-CD). Utilizing IC for N-chloroglycine measurement allows this method to be incorporated into routine monitoring of drinking water anions. For improving the sensitivity, IC was coupled with post-column reaction and UV detection (IC-PCR-UV), which was based on iodide oxidation by N-chloroglycine resulting in triiodide. The method performance was quantified by comparison of the results with the N,N-diethyl-p-phenylenediamine (DPD) method due to the unavailability of an N-chloroglycine standard. The N-chloroglycine method showed limits of quantification (LOQ) of 24 μg L(−1) Cl(2) and 13 μg L(−1) Cl(2) for IC-CD and IC-PCR-UV, respectively. These values were lower than those of DPD achieved in this research and in ultrapure water. Measurement of FAC in the drinking water matrix showed comparable robustness and sensitivity with statistically equivalent concentration that translated to recoveries of 102% for IC-CD and 105% for IC-PCR-UV. Repeatability and reproducibility performance were enhanced in the order of DPD, IC-CD, and IC-PCR-UV. Measurement of intrinsic FAC in the ClO(2) application revealed that the N-chloroglycine method performed considerably better in such a system where different oxidant species (ClO(2), FAC, chlorite, etc.) were present. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-020-02885-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7550385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-75503852020-10-19 Determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger Abdighahroudi, Mohammad Sajjad Schmidt, Torsten C. Lutze, Holger V. Anal Bioanal Chem Paper in Forefront Free available chlorine (FAC) is the most widely used chemical for disinfection and in secondary disinfection; a minimum chlorine residual must be present in the distribution system. FAC can also be formed as an impurity in ClO(2) production as well as a secondary oxidant in the ClO(2) application, which has to be monitored. In this study, a new method is developed based on the reaction of FAC with glycine in which the amine group selectively scavenges FAC and the N-chloroglycine formed can be measured by ion chromatography with conductivity detector (IC-CD). Utilizing IC for N-chloroglycine measurement allows this method to be incorporated into routine monitoring of drinking water anions. For improving the sensitivity, IC was coupled with post-column reaction and UV detection (IC-PCR-UV), which was based on iodide oxidation by N-chloroglycine resulting in triiodide. The method performance was quantified by comparison of the results with the N,N-diethyl-p-phenylenediamine (DPD) method due to the unavailability of an N-chloroglycine standard. The N-chloroglycine method showed limits of quantification (LOQ) of 24 μg L(−1) Cl(2) and 13 μg L(−1) Cl(2) for IC-CD and IC-PCR-UV, respectively. These values were lower than those of DPD achieved in this research and in ultrapure water. Measurement of FAC in the drinking water matrix showed comparable robustness and sensitivity with statistically equivalent concentration that translated to recoveries of 102% for IC-CD and 105% for IC-PCR-UV. Repeatability and reproducibility performance were enhanced in the order of DPD, IC-CD, and IC-PCR-UV. Measurement of intrinsic FAC in the ClO(2) application revealed that the N-chloroglycine method performed considerably better in such a system where different oxidant species (ClO(2), FAC, chlorite, etc.) were present. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-020-02885-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-09-18 2020 /pmc/articles/PMC7550385/ /pubmed/32944811 http://dx.doi.org/10.1007/s00216-020-02885-1 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 | Paper in Forefront Abdighahroudi, Mohammad Sajjad Schmidt, Torsten C. Lutze, Holger V. Determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger |
title | Determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger |
title_full | Determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger |
title_fullStr | Determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger |
title_full_unstemmed | Determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger |
title_short | Determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger |
title_sort | determination of free chlorine based on ion chromatography—application of glycine as a selective scavenger |
topic | Paper in Forefront |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550385/ https://www.ncbi.nlm.nih.gov/pubmed/32944811 http://dx.doi.org/10.1007/s00216-020-02885-1 |
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