ABSTRACT
Silicone rubber (SR)-based solid-contact ion-selective electrodes (ISEs) have been prepared for the first time with an electrically conducting polymer as the solid-contact (SC) layer. The Ca(2+)- and Ag(+)-selective electrodes were based on the ionophores ETH 1001 and o-xylylenebis(N,N-diisobutyl dithiocarbamate), respectively, integrated in room temperature vulcanizing silicone rubber (RTV 3140). The SC consisted of a polyaniline nanoparticle dispersion, which was found to considerably lower the impedance of the SCISEs in comparison to the SR-based coated wire electrodes (CWE). For the CaSCISEs, the bulk membrane resistance decreased from 700 MΩ (CaCWE) to 35 MΩ. Both the Ca(2+)- and Ag(+)-selective SCISEs exhibited nanomolar detection limits with fast Nernstian responses down to 10(-8) M. The potential response of the SCISEs was not influenced by light. The selectivities of the CaSCISEs were similar and for the AgSCISE better than their plasticized PVC-based analogues. Thus, SR seems to be a viable alternative to PVC membranes in ISE applications that require low water uptake, good adhesion, and robust and fast potential responses at submicromolar sample concentrations.
ABSTRACT
For the first time, FTIR-ATR spectroscopy was used to study the water uptake and its diffusion in ion-selective membranes (ISMs) based on poly(acrylates) (PAs) and silicone rubber (SR), which are emerging materials for the fabrication of ISMs for ultratrace analysis. Three different types of PA membranes were studied, consisting of copolymers of methyl methacrylate with n-butyl acrylate, decyl methacrylate, or isodecyl acrylate. Numerical simulations with the finite difference method showed that in most cases the water uptake of the PA and SR membranes could be described with a model consisting of two diffusion coefficients. The diffusion coefficients of the PA membranes were approximately 1 order of magnitude lower than those of plasticized poly(vinyl chloride) (PVC)-based ISMs and only slightly influenced by the membrane matrix composition. However, the simulations indicated that during longer contact times, the water uptake of PA membranes was considerably higher than that for plasticized PVC membranes. Although the diffusion coefficients of the SR and plasticized PVC membranes were similar, the SR membranes had the lowest water uptake of all membranes. This can be beneficial in preventing the formation of detrimental water layers in all-solid-state ion-selective electrodes. With FTIR-ATR, one can monitor the accumulation of different forms of water, i.e., monomeric, dimeric, clustered, and bulk water.
