Noise analysis;
Liquid/liquid interface;
Ion transfer kinetics;
Ac impedance;
IMMISCIBLE ELECTROLYTE-SOLUTIONS;
FLUCTUATION ANALYSIS;
FARADAIC IMPEDANCE;
LIQUID-LIQUID;
D O I:
10.1016/j.elecom.2015.04.006
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
Fluctuation analysis was utilized to determine the TEA ion transfer kinetics across the water/1,2-dichloroethane interface. The obtained data were compared with those derived from electrochemical impedance spectroscopy experiments using the same electrolytic cell. The apparent standard rate constants k(s), determined by these two techniques have a similar value. The average value k(s) = 0.37 cm s(-1) is comparable with the previously reported value k(s) = 0.2 cm s(-1). The experimental approach utilizing a thick wall glass micro-capillary to fix the interface exhibits a very small stray capacitance value, proving this system to be suitable for determining the kinetics of the fast ion transfer across a liquid/liquid interface. Application of a method employing a small perturbation signal prevents polarization of the inner capillary surface by current flowing through the cell. The induced polarization of the capillary can affect ion concentration at the interface due to electroosmosis and thus make the kinetic data evaluation difficult or erroneous. (C) 2015 Elsevier B.V. All rights reserved.