Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation

Characterization of the interaction of a urea-functionalized calix[4]arene ionophore and phosphate wasundertaken by combination of nuclear magnetic resonance (NMR) spectrometry, potentiometric selectivity coefficient evaluation and voltammetric ion transfer at the interface between two immiscibleele...

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Main Authors: Kivlehan, F., Mace, W., Moynihan, H., Arrigan, Damien
Format: Journal Article
Published: Pergamon-Elsevier Science Ltd 2009
Online Access:http://hdl.handle.net/20.500.11937/14044
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author Kivlehan, F.
Mace, W.
Moynihan, H.
Arrigan, Damien
author_facet Kivlehan, F.
Mace, W.
Moynihan, H.
Arrigan, Damien
author_sort Kivlehan, F.
building Curtin Institutional Repository
collection Online Access
description Characterization of the interaction of a urea-functionalized calix[4]arene ionophore and phosphate wasundertaken by combination of nuclear magnetic resonance (NMR) spectrometry, potentiometric selectivity coefficient evaluation and voltammetric ion transfer at the interface between two immiscibleelectrolyte solutions (ITIES). NMR revealed that the urea protons were involved in complexation withthe target anion and potentiometric separate solution selectivity data indicated selectivity for phosphateover chloride and sulphate. Voltammetry at the ITIES confirmed that the ionophore-facilitated transfer ofmonohydrogen phosphate occurred in preference to dihydrogen phosphate transfer. The results correlatewith previously reported data on the potentiometric evaluation of this calixarene as an anionophore inPVC-membrane electrodes. The data provide the basis for development of amperometric monohydrogenphosphate sensors based on the ion-transfer principle.
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:06:15Z
publishDate 2009
publisher Pergamon-Elsevier Science Ltd
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spelling curtin-20.500.11937-140442017-02-28T01:26:26Z Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation Kivlehan, F. Mace, W. Moynihan, H. Arrigan, Damien Characterization of the interaction of a urea-functionalized calix[4]arene ionophore and phosphate wasundertaken by combination of nuclear magnetic resonance (NMR) spectrometry, potentiometric selectivity coefficient evaluation and voltammetric ion transfer at the interface between two immiscibleelectrolyte solutions (ITIES). NMR revealed that the urea protons were involved in complexation withthe target anion and potentiometric separate solution selectivity data indicated selectivity for phosphateover chloride and sulphate. Voltammetry at the ITIES confirmed that the ionophore-facilitated transfer ofmonohydrogen phosphate occurred in preference to dihydrogen phosphate transfer. The results correlatewith previously reported data on the potentiometric evaluation of this calixarene as an anionophore inPVC-membrane electrodes. The data provide the basis for development of amperometric monohydrogenphosphate sensors based on the ion-transfer principle. 2009 Journal Article http://hdl.handle.net/20.500.11937/14044 Pergamon-Elsevier Science Ltd restricted
spellingShingle Kivlehan, F.
Mace, W.
Moynihan, H.
Arrigan, Damien
Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation
title Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation
title_full Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation
title_fullStr Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation
title_full_unstemmed Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation
title_short Study of electrochemical phosphate sensing systems: Spectrometric, potentiometric and voltammetric evaluation
title_sort study of electrochemical phosphate sensing systems: spectrometric, potentiometric and voltammetric evaluation
url http://hdl.handle.net/20.500.11937/14044