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Calibration-free analysis with chronoamperometry at microelectrodes

Calibration-free analysis with chronoamperometry at microelectrodes
Calibration-free analysis with chronoamperometry at microelectrodes

Analytical methods are crucial for monitoring and assessing the concentration of important chemicals, and there is now a growing demand for methodologies that allow miniaturization, require lower sample volumes, and enable real-time analysis in the field. Most electroanalytical techniques depend on calibrations or standards, and this has several limitations, ranging from matrix interference, to stability problems, time required, cost and waste. Therefore, strategies that do not require standards or calibration curves greatly interest the analytical chemistry community. Here, we propose a new quantification method that does not rely on calibration and is only based on a single chronoamperometric curve recorded with a microelectrode. We show that satisfactory analytical information is obtained with just one chronoamperometric experiment that only takes a few seconds. We propose different data treatments to determine the unknown concentration, we consider the experimental conditions and instrument parameters, we report how parallel reactions affect the results, and we recommend procedures to implement the method in autonomous sensors. We also show that the concentration of several species can be derived if their E° values are sufficiently far apart or the sum of all concentrations if the E° values are too close. The proposed method was validated with a model redox system then further evaluated by determining ascorbic acid concentrations in standard solutions and food supplements, and paracetamol in a pain killer. The results for ascorbic acid were compared with those obtained by coulometry, and a good agreement was found, with a maximum deviation ca. 10.8%. The approach was also successfully applied to ascorbic acid quantification in solutions with different viscosity using ethylene glycol as a thickener.

0003-2700
14766-14774
Conceição, Valdomiro S.
98d0ce88-e06b-4eff-b0c4-9c2c394a9fdf
Saraiva, Douglas P.M.
9c60fdd4-0ec4-4338-9094-bd40783caba0
Denuault, Guy
5c76e69f-e04e-4be5-83c5-e729887ffd4e
Bertotti, Mauro
76ebbd15-2368-42d5-a92e-ab34d0952300
Conceição, Valdomiro S.
98d0ce88-e06b-4eff-b0c4-9c2c394a9fdf
Saraiva, Douglas P.M.
9c60fdd4-0ec4-4338-9094-bd40783caba0
Denuault, Guy
5c76e69f-e04e-4be5-83c5-e729887ffd4e
Bertotti, Mauro
76ebbd15-2368-42d5-a92e-ab34d0952300

Conceição, Valdomiro S., Saraiva, Douglas P.M., Denuault, Guy and Bertotti, Mauro (2024) Calibration-free analysis with chronoamperometry at microelectrodes. Analytical Chemistry, 96 (37), 14766-14774. (doi:10.1021/acs.analchem.4c01645).

Record type: Article

Abstract

Analytical methods are crucial for monitoring and assessing the concentration of important chemicals, and there is now a growing demand for methodologies that allow miniaturization, require lower sample volumes, and enable real-time analysis in the field. Most electroanalytical techniques depend on calibrations or standards, and this has several limitations, ranging from matrix interference, to stability problems, time required, cost and waste. Therefore, strategies that do not require standards or calibration curves greatly interest the analytical chemistry community. Here, we propose a new quantification method that does not rely on calibration and is only based on a single chronoamperometric curve recorded with a microelectrode. We show that satisfactory analytical information is obtained with just one chronoamperometric experiment that only takes a few seconds. We propose different data treatments to determine the unknown concentration, we consider the experimental conditions and instrument parameters, we report how parallel reactions affect the results, and we recommend procedures to implement the method in autonomous sensors. We also show that the concentration of several species can be derived if their E° values are sufficiently far apart or the sum of all concentrations if the E° values are too close. The proposed method was validated with a model redox system then further evaluated by determining ascorbic acid concentrations in standard solutions and food supplements, and paracetamol in a pain killer. The results for ascorbic acid were compared with those obtained by coulometry, and a good agreement was found, with a maximum deviation ca. 10.8%. The approach was also successfully applied to ascorbic acid quantification in solutions with different viscosity using ethylene glycol as a thickener.

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More information

Accepted/In Press date: 26 August 2024
e-pub ahead of print date: 3 September 2024
Published date: 17 September 2024

Identifiers

Local EPrints ID: 494579
URI: http://eprints.soton.ac.uk/id/eprint/494579
ISSN: 0003-2700
PURE UUID: 9db98961-ab68-406c-9ba8-96b6a79e1da3
ORCID for Guy Denuault: ORCID iD orcid.org/0000-0002-8630-9492

Catalogue record

Date deposited: 10 Oct 2024 16:49
Last modified: 11 Oct 2024 01:33

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Contributors

Author: Valdomiro S. Conceição
Author: Douglas P.M. Saraiva
Author: Guy Denuault ORCID iD
Author: Mauro Bertotti

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