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Reagentless Acid–Base Titration for Alkalinity Detection in Seawater

[Image: see text] Herein, we report on a reagentless electroanalytical methodology for automatized acid–base titrations of water samples that are confined into very thin spatial domains. The concept is based on the recent discovery from our group ( A. WiorekAnal. Chem.2019, 91, 14951−1495931691565),...

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Autores principales: Wiorek, Alexander, Hussain, Ghulam, Molina-Osorio, Andres F., Cuartero, Maria, Crespo, Gaston A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552213/
https://www.ncbi.nlm.nih.gov/pubmed/34652903
http://dx.doi.org/10.1021/acs.analchem.1c02545
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author Wiorek, Alexander
Hussain, Ghulam
Molina-Osorio, Andres F.
Cuartero, Maria
Crespo, Gaston A.
author_facet Wiorek, Alexander
Hussain, Ghulam
Molina-Osorio, Andres F.
Cuartero, Maria
Crespo, Gaston A.
author_sort Wiorek, Alexander
collection PubMed
description [Image: see text] Herein, we report on a reagentless electroanalytical methodology for automatized acid–base titrations of water samples that are confined into very thin spatial domains. The concept is based on the recent discovery from our group ( A. WiorekAnal. Chem.2019, 91, 14951−1495931691565), in which polyaniline (PANI) films were found to be an excellent material to release a massive charge of protons in a short time, achieving hence the efficient (and controlled) acidification of a sample. We now demonstrate and validate the analytical usefulness of this approach with samples collected from the Baltic Sea: the titration protocol indeed acts as an alkalinity sensor via the calculation of the proton charge needed to reach pH 4.0 in the sample, as per the formal definition of the alkalinity parameter. In essence, the alkalinity sensor is based on the linear relationship found between the released charge from the PANI film and the bicarbonate concentration in the sample (i.e., the way to express alkalinity measurements). The observed alkalinity in the samples presented a good agreement with the values obtained by manual (classical) acid–base titrations (discrepancies <10%). Some crucial advantages of the new methodology are that titrations are completed in less than 1 min (end point), the PANI film can be reused at least 74 times over a 2 week period (<5% of decrease in the released charge), and the utility of the PANI film to even more decrease the final pH of the sample (pH ∼2) toward applications different from alkalinity detection. Furthermore, the acidification can be accomplished in a discrete or continuous mode depending on the application demands. The new methodology is expected to impact the future digitalization of in situ acid–base titrations to obtain high-resolution data on alkalinity in water resources.
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spelling pubmed-85522132021-10-29 Reagentless Acid–Base Titration for Alkalinity Detection in Seawater Wiorek, Alexander Hussain, Ghulam Molina-Osorio, Andres F. Cuartero, Maria Crespo, Gaston A. Anal Chem [Image: see text] Herein, we report on a reagentless electroanalytical methodology for automatized acid–base titrations of water samples that are confined into very thin spatial domains. The concept is based on the recent discovery from our group ( A. WiorekAnal. Chem.2019, 91, 14951−1495931691565), in which polyaniline (PANI) films were found to be an excellent material to release a massive charge of protons in a short time, achieving hence the efficient (and controlled) acidification of a sample. We now demonstrate and validate the analytical usefulness of this approach with samples collected from the Baltic Sea: the titration protocol indeed acts as an alkalinity sensor via the calculation of the proton charge needed to reach pH 4.0 in the sample, as per the formal definition of the alkalinity parameter. In essence, the alkalinity sensor is based on the linear relationship found between the released charge from the PANI film and the bicarbonate concentration in the sample (i.e., the way to express alkalinity measurements). The observed alkalinity in the samples presented a good agreement with the values obtained by manual (classical) acid–base titrations (discrepancies <10%). Some crucial advantages of the new methodology are that titrations are completed in less than 1 min (end point), the PANI film can be reused at least 74 times over a 2 week period (<5% of decrease in the released charge), and the utility of the PANI film to even more decrease the final pH of the sample (pH ∼2) toward applications different from alkalinity detection. Furthermore, the acidification can be accomplished in a discrete or continuous mode depending on the application demands. The new methodology is expected to impact the future digitalization of in situ acid–base titrations to obtain high-resolution data on alkalinity in water resources. American Chemical Society 2021-10-15 2021-10-26 /pmc/articles/PMC8552213/ /pubmed/34652903 http://dx.doi.org/10.1021/acs.analchem.1c02545 Text en © 2021 The Authors. Published by 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 Wiorek, Alexander
Hussain, Ghulam
Molina-Osorio, Andres F.
Cuartero, Maria
Crespo, Gaston A.
Reagentless Acid–Base Titration for Alkalinity Detection in Seawater
title Reagentless Acid–Base Titration for Alkalinity Detection in Seawater
title_full Reagentless Acid–Base Titration for Alkalinity Detection in Seawater
title_fullStr Reagentless Acid–Base Titration for Alkalinity Detection in Seawater
title_full_unstemmed Reagentless Acid–Base Titration for Alkalinity Detection in Seawater
title_short Reagentless Acid–Base Titration for Alkalinity Detection in Seawater
title_sort reagentless acid–base titration for alkalinity detection in seawater
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552213/
https://www.ncbi.nlm.nih.gov/pubmed/34652903
http://dx.doi.org/10.1021/acs.analchem.1c02545
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