Determination of Water Uptake of Polymeric Ion-Selective Membranes with the Coulometric Karl Fischer and FT-IR-Attenuated Total Reflection Techniques

    Tutkimustuotos: LehtiartikkeliArtikkeliTieteellinenvertaisarvioitu

    32 Sitaatiot (Scopus)

    Abstrakti

    The water uptake of plasticized poly(vinyl chloride) (PVC) and silicone rubber (SR) based calcium-selective membranes which are commonly used in solid-contact and coated-wire ion-selective electrodes (SC-ISEs and CWEs) was quantified with the oven based coulometric Karl Fischer (KF) technique. Two different membrane types were studied: (1) the plasticized PVC or SR (RTV 3140) membrane matrix without other added membrane components and (2) the full Ca2+-selective membrane formulation consisting of the membrane matrixes, potassium tetrakis[3,5-bis(trifluoromethyl)-phenyl]borate and calcium ionophore IV (ETH 5234) or calcium ionophore I (ETH 1001). The membranes were contacted for 24 h either asymmetrically from one side or symmetrically from both sides with deionized water (DIW) or 0.1 M solutions of CaCl2, KCl, or NaCl. It was found that the water uptake was higher for symmetrically contacted membranes. The highest water uptake (0.15-0.17 wt %) was obtained for the plasticized PVC based Ca2+-selective membranes in DIW, whereas the water uptake was lower in 0.1 M electrolyte solutions. Symmetrically contacted Ca2+-selective SR membranes had much lower water uptake in 0.1 M CaCl2 (0.03 wt %) than their plasticized PVC counterparts (0.1 wt %). However, the (noncontacted) SR membranes contained initially much more water (0.09-0.15 wt %) than the PVC membranes (0.04-0.07 wt %). Furthermore, in good accordance with the KF measurements, it was verified with FT-IR-attenuated total reflection (ATR) spectroscopy that the water content at the substrate/membrane interface and consequently in the whole membrane was influenced by the electrolyte solution.
    AlkuperäiskieliEi tiedossa
    Sivut1006–1012
    Sivumäärä7
    JulkaisuAnalytical Chemistry
    Vuosikerta85
    Numero2
    DOI - pysyväislinkit
    TilaJulkaistu - 2013
    OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

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