Perchlorate selective membrane electrodes based on synthesized platinum(II) complexes for low-level concentration measurements
Three synthesized platinum(II) complexes, [PtR 2(NN)] (R = Me, p-MeC 6H 4 and p-MeOC 6H 4; NN = 2,2′-bipyridyl), were studied to characterize their ability as an anion carrier in a PVC membrane electrode. The polymeric membrane electrodes (PME) and also coated glassy carbon electrodes (CGCE) prepare...
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Published in: | Sensors and actuators. B, Chemical Vol. 120; no. 2; pp. 447 - 454 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier B.V
10-01-2007
|
Subjects: | |
Online Access: | Get full text |
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Summary: | Three synthesized platinum(II) complexes, [PtR
2(NN)] (R
=
Me,
p-MeC
6H
4 and
p-MeOC
6H
4; NN
=
2,2′-bipyridyl), were studied to characterize their ability as an anion carrier in a PVC membrane electrode. The polymeric membrane electrodes (PME) and also coated glassy carbon electrodes (CGCE) prepared with [Pt(
p-MeOC
6H
4)
2(NN)] showed excellent response characteristics to perchlorate ions. The electrodes exhibited Nernstian responses to ClO
4
− ions over a wide concentration range from 5
×
10
−7 to 4.0
×
10
−1
M for PME and 1.5
×
10
−7 to 2.7
×
10
−1
M for CGCE with low detection limits (4.0
×
10
−7
M for PME and 1.0
×
10
−7
M for CGCE). The electrodes possess fast response time, satisfactory reproducibility, appropriate lifetime and, most importantly, good selectivity toward ClO
4
− relative to a variety of other common anions. The potentiometric response of the electrodes is independent of the pH of the test solution in the pH range 2.5–9.5. The proposed sensors were used in potentiometric determination of perchlorate ions in mineral water, urine samples and also samples containing interfering anions. The interaction of the ionophore with perchlorate ions was shown by UV–vis spectroscopy. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0925-4005 1873-3077 |
DOI: | 10.1016/j.snb.2006.02.036 |