Development of 5,5′‐Bi(1,10‐Phenanthroline)‐Based PVC Membrane Potentiometric Sensor for Silver Determination

In this study, the selectivity of the 5.5'-bi(1,10-phenanthroline) Compound (1) against Ag<sup>+</sup> ions as a chemical sensor was investigated by both absorption and potentiometric methods. First, a 1 × 10<sup>-5</sup> M solution of Compound (1) in acetonitrile was prepared. For the selectivity test, 1 × 10<sup>-2</sup> M solutions of metal ions in acetonitrile were prepared. UV-visible absorption measurements were performed by adding metal ions to a 5.5'-bi(1,10-phenanthroline) compound at certain concentrations. Among the studied metal ions, it was found to be selective only against silver ions. In addition, solid-state contact polyvinylchloride (PVC) membrane electrodes prepared using 5.5'-bi(1,10-phenanthroline) as an ionophore were found to be selective against Ag<sup>+</sup> ions among other ions. The optimum membrane composition of the measurement was determined as 3% 5.5'-bi(1,10-phenanthroline) + 32% PVC + 64% o-nitrophenyl octyl ether (o-NPOE) + 1% potassium tetrakis(4-chlorophenyl) borate (KTpClPB). The potentiometric properties of the silver selective electrode were determined as linear working range 1.0 × 10<sup>-7</sup>-1.0 × 10<sup>-3</sup> M, detection limit 1.0 × 10<sup>-7</sup> M, pH working range 3.23-9.08, and response time 3 s. Absorption and potentiometric methods confirm the selectivity towards silver ions. The IRC analysis of the silver-containing complex, performed using the DFT/B3LYP method with the LanL2DZ basis set, reveals an activation energy of approximately 0.002 Eh, with the transition state energy at -1.433173 Eh.

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Publication Details

Journal
Luminescence
Published
2025-02-27
DOI
https://doi.org/10.1002/bio.70136
Citations
3
Primary Topic
Analytical Chemistry and Sensors
Type
article
Field-Weighted Citation Impact
2.21
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article

Development of 5,5′‐Bi(1,10‐Phenanthroline)‐Based PVC Membrane Potentiometric Sensor for Silver Determination

Derya Güngördü Solğun, Gülşah Saydan Kanberoğlu, Mehmet Salih Ağırtaş, Nuray Kaya
3 citations
Luminescence
Analytical Chemistry and Sensors
2.21
article

Development of 5,5′‐Bi(1,10‐Phenanthroline)‐Based PVC Membrane Potentiometric Sensor for Silver Determination

Derya Güngördü Solğun, Gülşah Saydan Kanberoğlu, Mehmet Salih Ağırtaş, Nuray Kaya
article en
3 citations

Abstract

In this study, the selectivity of the 5.5'-bi(1,10-phenanthroline) Compound (1) against Ag<sup>+</sup> ions as a chemical sensor was investigated by both absorption and potentiometric methods. First, a 1 × 10<sup>-5</sup> M solution of Compound (1) in acetonitrile was prepared. For the selectivity test, 1 × 10<sup>-2</sup> M solutions of metal ions in acetonitrile were prepared. UV-visible absorption measurements were performed by adding metal ions to a 5.5'-bi(1,10-phenanthroline) compound at certain concentrations. Among the studied metal ions, it was found to be selective only against silver ions. In addition, solid-state contact polyvinylchloride (PVC) membrane electrodes prepared using 5.5'-bi(1,10-phenanthroline) as an ionophore were found to be selective against Ag<sup>+</sup> ions among other ions. The optimum membrane composition of the measurement was determined as 3% 5.5'-bi(1,10-phenanthroline) + 32% PVC + 64% o-nitrophenyl octyl ether (o-NPOE) + 1% potassium tetrakis(4-chlorophenyl) borate (KTpClPB). The potentiometric properties of the silver selective electrode were determined as linear working range 1.0 × 10<sup>-7</sup>-1.0 × 10<sup>-3</sup> M, detection limit 1.0 × 10<sup>-7</sup> M, pH working range 3.23-9.08, and response time 3 s. Absorption and potentiometric methods confirm the selectivity towards silver ions. The IRC analysis of the silver-containing complex, performed using the DFT/B3LYP method with the LanL2DZ basis set, reveals an activation energy of approximately 0.002 Eh, with the transition state energy at -1.433173 Eh.

LuminescenceVol. 40(3)
Van Yüzüncü Yıl Üniversitesi (TR)
Openalex Percentile: Top 14%
Analytical Chemistry and Sensors
2.21
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