Response characteristics of ion selective electrodes based on dinonylnaphthalenesulfonic acid

1980 ◽  
Vol 52 (3) ◽  
pp. 562-564 ◽  
Author(s):  
Charles R. Martin ◽  
Henry. Freiser

Chemosensors ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 4
Author(s):  
Ville Yrjänä ◽  
Indrek Saar ◽  
Mihkel Ilisson ◽  
Sandip A. Kadam ◽  
Ivo Leito ◽  
...  

Solid-contact ion-selective electrodes with carbazole-derived ionophores were prepared. They were characterized as acetate sensors, but can be used to determine a number of carboxylates. The potentiometric response characteristics (slope, detection limit, selectivity, and pH sensitivity) of sensors prepared with different membrane compositions (ionophore, ionophore concentration, anion exchanger concentration, and plasticizer) were evaluated. The results show that for the macrocyclic ionophores, a larger cavity provided better selectivity. The sensors exhibited modest selectivity for acetate but good selectivity for benzoate. The carbazole-derived ionophores effectively decreased the interference from lipophilic anions, such as bromide, nitrate, iodide, and thiocyanate. The selectivity, detection limit, and linear range were improved by choosing a suitable plasticizer and by reducing the ionophore and anion exchanger concentrations. The influence of the electrode body’s material upon the composition of the plasticized poly(vinyl chloride) membrane, and thus also upon the sensor characteristics, was also studied. The choice of materials for the electrode body significantly affected the characteristics of the sensors.



2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Shane Peper ◽  
Chad Gonczy

Cs+-selective solvent polymeric membrane-based ion-selective electrodes (ISEs) were developed by doping ethylene glycol-functionalized cross-linked polystyrene microspheres (P-EG) into a plasticized poly(vinyl chloride) (PVC) matrix containing sodium tetrakis-(3,5-bis(trifluoromethyl)phenyl) borate (TFPB) as the ion exchanger. A systematic study examining the effects of the membrane plasticizers bis(2-ethylhexyl) sebacate (DOS), 2-nitrophenyl octyl ether (NPOE), and 2-fluorophenyl nitrophenyl ether (FPNPE) on the potentiometric response and selectivity of the corresponding electrodes was performed. Under certain conditions, P-EG-based ion-selective electrodes (ISEs) containing TFPB and plasticized with NPOE exhibited a super-Nernstian response between1×10−3and1×10−4 M Cs+, a response characteristic not observed in analogous membranes plasticized with either DOS or FPNPE. Additionally, the performance of P-EG-based ISEs was compared to electrodes based on two mobile ionophores, a neutral lipophilic ethylene glycol derivative (ethylene glycol monooctadecyl ether (U-EG)) and a charged metallacarborane ionophore, sodium bis(dicarbollyl)cobaltate(III) (CC). In general, P-EG-based electrodes plasticized with FPNPE yielded the best performance, with a linear range from 10-1–10-5 M Cs+, a conventional lower detection limit of8.1×10−6 M Cs+, and a response slope of 57.7 mV/decade. The pH response of P-EG ISEs containing TFPB was evaluated for membranes plasticized with either NPOE or FPNPE. In both cases, the electrodes remained stable throughout the pH range 3–12, with only slight proton interference observed below pH 3.



2020 ◽  
Vol 24 (11-12) ◽  
pp. 2975-2983 ◽  
Author(s):  
Tingting Han ◽  
Zekra Mousavi ◽  
Ulriika Mattinen ◽  
Johan Bobacka

Abstract The chronoamperometric and coulometric response of solid contact ion-selective electrodes (SCISEs) for the detection of divalent cations was investigated in order to provide a more complete description of the mechanism of the recently introduced coulometric transduction method for SCISEs. The coulometric transduction method has earlier been employed only for SCISEs that were selective to monovalent ions. The SCISEs utilized poly(3,4-ethylenedioxythiophene) (PEDOT) doped with poly(styrene sulfonate) (PSS−) as the solid contact (ion-to-electron transducer). PEDOT(PSS) was electrodeposited on glassy carbon and covered with plasticized PVC-based ion-selective membranes (ISMs) that were selective towards divalent cations (Ca2+, Pb2+). In contrast to earlier studies, the results obtained in this work show that the coulometric response for the Pb2+-SCISE was limited mainly by ion transport in the PEDOT(PSS) layer, which was not the case for the Ca2+-SCISE, nor was it observed earlier for the monovalent ions. The exceptional behavior of the Pb2+-SCISE was explored further by electrochemical impedance spectroscopy, and it was shown that the effective redox capacitance of PEDOT(PSS) was significantly higher for the Pb2+-SCISE than for the Ca2+-SCISE although the polymerization charge of PEDOT(PSS) was the same. The slow transport of Pb2+ in PEDOT(PSS) was tentatively related to complexation between Pb2+ and PEDOT(PSS).





1980 ◽  
Vol 52 (5) ◽  
pp. 384-384
Author(s):  
Gerald L. Vogel ◽  
W. E. Brown


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