scholarly journals Characterization of a Ag+-Selective Electrode Based on Naphthalimide Derivative as Ionophore

2020 ◽  
Vol 17 ◽  
pp. 30-34
Author(s):  
Zhang Jun ◽  
Chen Qiwei ◽  
Zhang Wenting ◽  
Yu Chunwei ◽  
Zhang Qinnan ◽  
...  

A naphthalimide derivative has been explored as neutral ionophore for Ag+-selective electrode. Potentiometric response revealed that electrode based on the proposed ionophore with 2-nitrophenyl octyl ether as solvent in a poly (vinyl chloride) membrane matrix shows a measuring range of 1.0×10-6-1.0×10-2 M with a slope of 50.4±0.3 mV/decade. This electrode has high selectivity to Ag+ with respect to alkaline, alkaline earth and other heavy metal ions.

2015 ◽  
Vol 11 (8) ◽  
pp. 3798-3803
Author(s):  
M. H. Fekri ◽  
Maryam Darvishpour ◽  
M. Chegeni ◽  
H Dashti Khavidaki

A novel ion-selective poly(vinyl chloride) membrane sensor for Fe(III) ions based on Tris-(1,2-diiminocyclohexylmethyl-5-Cl-2-hydroxyl benzaldehyde) are reported in this paper. The electrode exhibits a good potentiometric response for Fe(III), response time ≤ 20 s, over a wide concentration range 1.0 × 10-5 to 1.0 × 10-1 M with a slope 19.4 ± 0.5 mV/decade. The potentiometric response is independent on the pH of solution in the range of 1.5-5.0. The proposed electrode can be used for at least two months without any considerable divergence in potentials.It exhibits very good selectivity relative to a wide variety of alkali, alkaline earth, transition and heavy metal ions. The electrode assembly was also used as indicator electrode in the potentiometric titration of Fe(III) with EDTA.


2011 ◽  
Vol 8 (s1) ◽  
pp. S203-S210 ◽  
Author(s):  
Hassan Ali Zamani ◽  
Zynab Rafati ◽  
Soraia Meghdadi

In this work, we report as new Tb3+-PVC membrane sensor based onN,N’-bis(pyrrolylmethylene)- 2-aminobenzylamine (PMA) as a suitable ion carrier. Poly vinylchloride (PVC)-based membrane composed of PMA with oleic acid (OA) as anionic additives and acetophenone (AP) as plasticizing solvent mediators. The Tb3+sensor exhibits a Nernstian slope of 19.7±0.4 mV per decade over the concentration range of 1.0×10-5to 1.0×10-2M and a detection limit of 4.6×10-6M of Tb3+ions. The potentiometric response of the sensor is independent of the solution pH in the range of 2.9–8.1. It has a very short response time, in the whole concentration range (∼5 s). The recommended sensor revealed comparatively good selectivity with respect to most alkali, alkaline earth, some transition and heavy metal ions. It was successfully employed as an indicator electrode in the potentiometric titration of Tb(III) ions with EDTA. The electrode was also employed for the determination of the fluoride ion in two mouth wash preparations and the determination of Tb3+ions concentration in mixtures of three different ions.


2007 ◽  
Vol 72 (9) ◽  
pp. 1189-1206 ◽  
Author(s):  
Hassan Ali Zamani ◽  
Mohammad Reza Ganjali ◽  
Nasim Seifi

A Dy(III) ion-selective electrode based on 6-hydrazino-1,5-diphenyl-6,7-dihydropyrazolo[3,4-d]pyrimidine-4(5H)-imine (HDDPI) as an excellent sensing material was developed. The sensor exhibits a Nernstian behavior (a slope of 19.6 ± 0.3 mV per decade) over a wide concentration range (from 1.0 × 10-1 to 8.0 × 10-7 M Dy) with a detection limit of 4.2 × 10-7 M. The sensor response is independent of pH of the solution in the pH range 3.5-8.3. The sensor possesses the advantages of short conditioning time, fast response time (<10 s) and in particular, good selectivity and sensitivity to the dysprosium ion in the presence of a variety of cations, including alkali, alkaline earth, transition and heavy metal ions. The sensor also showed a great enhancement in selectivity coefficients for dysprosium ions, in comparison with the formerly mentioned dysprosium sensors. The electrode can be used for at least 10 weeks without any considerable divergence in the potentials. The proposed electrode was successfully used as an indicator electrode in potentiometric titration of Dy(III) ions with EDTA. The membrane sensor was also used in the determination of concentration of F- ions in some mouth washing solutions and in the Dy3+ recovery from solution.


2012 ◽  
Vol 9 (4) ◽  
pp. 1941-1950 ◽  
Author(s):  
Hassan Ali Zamani ◽  
Mojdeh Zaferoni ◽  
Soraia Meghdadi

The N-benzoylethylidene-2-aminobenzylamine (BEA) was used as a suitable ionophore in construction of neodymium ion selective electrode. The electrode with composition of 30% PVC, 58% solvent mediator (NB), 2% ionophore (BEA) and 10% anionic additive (OA) shows the best potentiometric response characteristics. The Nd3+sensor exhibits a Nernstian slope of 21.2 ± 0.2 mV decade-1over the concentration range of 1.0 × 10-6to 1.0 × 10-2mol L-1, and a detection limit of 6.3 × 10-7mol L-1of Nd3+ions. The potentiometric response of the sensor is independent of the solution pH in the range of 2.4–8.5. It has a very short response time, in the whole concentration range (~7 s), and can be used for at least eight weeks. The proposed sensor revealed high selectivity with respect to all common alkali, alkaline earth, transition and heavy metal ions, including members of the lanthanide family other than Nd3+. The Nd3+sensor was successfully applied as an indicator electrode in the potentiometric titration of Nd3+ions with EDTA. The electrode was also employed for the determination of the fluoride ion in two mouth wash preparations.


2021 ◽  
Vol 40 (1) ◽  
pp. 127-135
Author(s):  
Khaled Elgendy ◽  
Mohamed A.F. Elmosallamy ◽  
Moustafa K. Soltan ◽  
Alaa S. Amin ◽  
Dina S. Elshaprawy

Abstract Two new potentiometric sensors were created for the quantification of bisoprolol fumarate and alverine citrate in bulk pharmaceutical dosage forms and human serum. Bisoprolol and alverine sensors were manufactured by combining potassium tetrakis (p-chlorophenyl) borate ion pairs to serve as electroactive substances, plasticized poly (vinyl chloride) matrix membranes, and o-nitrophenyl octyl ether. They demonstrated high responses over the concentration ranges of 1.0×10−6 to 1.0×10−2 mol L−1 bisoprolol and alverine with close to Nernstian cationic slopes of 52 and 56 mV decade−1, respectively. The detection limits for bisoprolol and alverine were 2.6×10−6 and 1.75×10−6 mol L−1, respectively. For both medications, the response time was instantaneous (2.0 s). The working pH ranges for bisoprolol and alverine were 4.50–8.50 and 2.00–8.80, respectively. For both sensors, the life cycle was long (3 months). The sensors were used in pharmaceutical dosage types for the assay of bisoprolol and alverine, recording average recoveries of 99.40% and 99.98% respectively and were also successfully used for estimating the two drugs in human serum with an average recovery of 99.60% for both drugs. For all multiple staged interfering materials, the reported latest potentiometric sensor methods displayed high selectivity. The current sensor obtained a high percentage recovery and an excellent relative standard deviation compared with those obtained from previously published methods.


2011 ◽  
Vol 8 (s1) ◽  
pp. S97-S104 ◽  
Author(s):  
Hassan Ali Zamani

2-(4-Oxopentan-2-ylideneamino) isoindoline-1,3-dione (OID) was found to be a suitable neutral ionophore in the fabrication of a highly selective Ho3+membrane sensor. The electrode has a near-Nernstian slope of 19.6±0.5 mV per decade with a wide concentration range between 1.0×10-6and 1.0×10-2mol/L in the pH range of 3.5–8.8, having a fast response time (∼5 s) and a detection limit of 5.8×10-7mol/L. This electrode presented very good selectivity and sensitivity towards the Ho3+ions over a wide variety of cations, including alkali, alkaline earth, transition and heavy metal ions. The practical utility of the electrode has been demonstrated by its use as an indicator electrode for the potentiometric titration of a Ho3+solution with EDTA and for the determination of Ho3+ions concentration in mixtures of two and three different ions.


2013 ◽  
Vol 11 (4) ◽  
pp. 554-560 ◽  
Author(s):  
Erhan Zor ◽  
Ahmet Saf ◽  
Haluk Bingol

AbstractA novel azocalix[4]arene derivative, 5,11,17,23-tetrakis[(acetophenone)azo]-25,26,27,28-tetrahydroxycalix[4]arene (APC4), containing acetophenone azo groups at the upper rim was synthesized as a chemosensor. Its binding and sensing properties with alkali and alkaline earth metal ions (Li+, Na+, K+, Rb+, Cs+, Mg2+, Ca2+, Sr2+, Ba2+) were investigated by UV-vis spectrophotometric and voltammetric techniques. The stoichiometric ratio and the association constant were determined spectrophotometrically as 1:1 and (1.94±0.31)×105 L mol−1 for the complex between Mg2+ and the chemosensor, respectively. Moreover, it was shown that the interaction between Mg2+ and the APC4 occurred by means of the phenol groups at the lower rim by voltammetric methods. The results of spectrophotometric and voltammetric experiments showed that the chromogenic chemosensor has high selectivity towards Mg2+ among the other used metal ions, especially the interfering Ca2+ ion.


Sign in / Sign up

Export Citation Format

Share Document