Electrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl-p-phenylenediamine in dimethylformamide
The electrochemical oxidation of DEPD proceeds via an ECrevECE mechanism in dimethylformamide. It has been investigated at elevated temperatures up to 130 °C at both micro and macro platinum and glassy carbon electrodes. Kinetic and thermodynamic parameters for the reaction process have been calcula...
Main Authors: | , , , , , , |
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Format: | Journal article |
Language: | English |
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2004
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author | Wildgoose, G Giovanelli, D Klymenko, O Lawrence, N Jiang, L Jones, T Compton, R |
author_facet | Wildgoose, G Giovanelli, D Klymenko, O Lawrence, N Jiang, L Jones, T Compton, R |
author_sort | Wildgoose, G |
collection | OXFORD |
description | The electrochemical oxidation of DEPD proceeds via an ECrevECE mechanism in dimethylformamide. It has been investigated at elevated temperatures up to 130 °C at both micro and macro platinum and glassy carbon electrodes. Kinetic and thermodynamic parameters for the reaction process have been calculated for each temperature. Further, the voltammetric response of DEPD shows enhanced limiting currents in the presence of sulfide. The analytical utility of the approach has been investigated with linear range from 50 to 850 μM sulfide concentration observed and a corresponding limit of detection of 20 μM achievable at temperatures of 70 °C. |
first_indexed | 2024-03-07T05:53:41Z |
format | Journal article |
id | oxford-uuid:e9c82e75-e8ac-474a-9e60-f09f136d2450 |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T05:53:41Z |
publishDate | 2004 |
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spelling | oxford-uuid:e9c82e75-e8ac-474a-9e60-f09f136d24502022-03-27T10:56:50ZElectrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl-p-phenylenediamine in dimethylformamideJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e9c82e75-e8ac-474a-9e60-f09f136d2450EnglishSymplectic Elements at Oxford2004Wildgoose, GGiovanelli, DKlymenko, OLawrence, NJiang, LJones, TCompton, RThe electrochemical oxidation of DEPD proceeds via an ECrevECE mechanism in dimethylformamide. It has been investigated at elevated temperatures up to 130 °C at both micro and macro platinum and glassy carbon electrodes. Kinetic and thermodynamic parameters for the reaction process have been calculated for each temperature. Further, the voltammetric response of DEPD shows enhanced limiting currents in the presence of sulfide. The analytical utility of the approach has been investigated with linear range from 50 to 850 μM sulfide concentration observed and a corresponding limit of detection of 20 μM achievable at temperatures of 70 °C. |
spellingShingle | Wildgoose, G Giovanelli, D Klymenko, O Lawrence, N Jiang, L Jones, T Compton, R Electrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl-p-phenylenediamine in dimethylformamide |
title | Electrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl-p-phenylenediamine in dimethylformamide |
title_full | Electrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl-p-phenylenediamine in dimethylformamide |
title_fullStr | Electrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl-p-phenylenediamine in dimethylformamide |
title_full_unstemmed | Electrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl-p-phenylenediamine in dimethylformamide |
title_short | Electrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl-p-phenylenediamine in dimethylformamide |
title_sort | electrochemical determination of sulfide at high temperatures via its electrochemically initiated reaction with diethyl p phenylenediamine in dimethylformamide |
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