TY - JOUR

T1 - Non-constancy of the bulk resistance of ionophore-based Cd2+-selective electrode

T2 - A correlation with the water uptake by the electrode membrane

AU - Kalinichev, Andrey V.

AU - Solovyeva, Elena V.

AU - Ivanova, Arina R.

AU - Khripoun, Galina A.

AU - Mikhelson, Konstantin N.

PY - 2020/2/20

Y1 - 2020/2/20

N2 - The dependence of the bulk resistance of Ion-selective electrodes (ISEs) on the concentration of aqueous solution is studied by means of chronopotentiometry and electrochemical impedance using Cd2+-ISE as model system. It is shown that within the Nernstian response range that bulk resistance of the ISE membrane increases along the dilution of the aqueous phase. The results are consistent with analogous studies carried out earlier with Ca2+, K+ and NO3 −-ISEs. Water uptake by the Cd2+-ISE membrane is studied systematically, and it is shown that the water uptake also increases along decrease of the concentration of CdCl2 solution. The shapes of the concentration dependence of the two properties: (1) the membrane bulk resistance and (2) the water uptake, are very similar, suggesting a correlation between (1) and (2). SEM/EDX studies of Cd2+-ISE membranes confirm uniform distribution of the components within dry membranes, except of surface layers which are enriched in plasticizer and depleted in the polymer. It is concluded that the ISE membranes equilibrated with aqueous solutions must be considered as non-homogeneous materials due to the presence of the dispersed water. It is assumed that the electrochemical equilibrium is established between the solution and the membrane organic phase proper, while the resistance refers to the membrane as a material including water droplets which hinder the charge transfer across the membranes.

AB - The dependence of the bulk resistance of Ion-selective electrodes (ISEs) on the concentration of aqueous solution is studied by means of chronopotentiometry and electrochemical impedance using Cd2+-ISE as model system. It is shown that within the Nernstian response range that bulk resistance of the ISE membrane increases along the dilution of the aqueous phase. The results are consistent with analogous studies carried out earlier with Ca2+, K+ and NO3 −-ISEs. Water uptake by the Cd2+-ISE membrane is studied systematically, and it is shown that the water uptake also increases along decrease of the concentration of CdCl2 solution. The shapes of the concentration dependence of the two properties: (1) the membrane bulk resistance and (2) the water uptake, are very similar, suggesting a correlation between (1) and (2). SEM/EDX studies of Cd2+-ISE membranes confirm uniform distribution of the components within dry membranes, except of surface layers which are enriched in plasticizer and depleted in the polymer. It is concluded that the ISE membranes equilibrated with aqueous solutions must be considered as non-homogeneous materials due to the presence of the dispersed water. It is assumed that the electrochemical equilibrium is established between the solution and the membrane organic phase proper, while the resistance refers to the membrane as a material including water droplets which hinder the charge transfer across the membranes.

KW - Bulk resistance

KW - Cadmium

KW - Correlation

KW - Ionophore-based ion-selective membranes

KW - Water uptake

KW - NERNST-PLANCK

KW - FTIR-ATR

KW - OPTODES

KW - MECHANISM

KW - STABILITY

KW - TRANSPORT

KW - COEXTRACTION

KW - ATTENUATED TOTAL-REFLECTION

KW - DIFFUSION

KW - ION-SELECTIVE ELECTRODES

UR - http://www.scopus.com/inward/record.url?scp=85077341248&partnerID=8YFLogxK

U2 - 10.1016/j.electacta.2019.135541

DO - 10.1016/j.electacta.2019.135541

M3 - Article

AN - SCOPUS:85077341248

VL - 334

JO - Electrochimica Acta

JF - Electrochimica Acta

SN - 0013-4686

M1 - 135541

ER -