Abstract

In this work, two types of optical sensors were prepared for the quantification of potassium: the bulk optode (BO) and nano-optode (NO). The BO was prepared using three main components: the ionophore valinomycin, the ion exchanger tetrakis(4-chlorophenyl) potassium borate (K-TCPB), and the chromoionophore ETH 5294 (CHI). The optimal composition was found to be in a ratio of [1 : 1 : 1]. The NO was prepared by miniaturizing the BO through sonication in surfactant Pluronic F-127. The working range for the linear calibration model of BO was from 10-6 to 1.0 M K+ with a LODBO = 0.31 μM, meanwhile for NO was from 10-4 to 1.0 M K+ with a LODNO = 30.3 μM. Both optodes were tested for selectivity towards K+ in the presence of alkaline and alkaline earth ions, with a selectivity coefficient > 1.0. Furthermore, precision and stability studies of BO and NO were performed for three levels of K+ concentrations, 10-6, 10-3, 1.0 M for BO and 10-4, 10-2, 1.0 M for NO, showing a good homogeneity of the NO in the whole concentration range. However, an excessive variability was obtained for BO at 1.0 M K+. Therefore, the NO represents a potential tool for quantification of K+.

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