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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2573-2581 
    ISSN: 0887-624X
    Keywords: single alkaline metal ion conductors ; polymer electrolytes ; antioxidation properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polysiloxanes with covalently attached oligo ethylene oxide and di-t-butylphenol (I), naphthol (II), and hexafluoropropanol (III) were synthesized. The crosslinked polymers with a hexamethylene spacer were also prepared. The ion conductivities of the Li, Na, and K salts were measured as a function of temperature. The highest conductivities for K and Na of I at 30°C were 5.5 × 10-5 and 5.0 × 10-5 S/cm, respectively, when the ratio of the ion to ethylene oxide unit was 0.014. On the other hand, Li conductivity was 8.0 × 10-6 S/cm when the ratio between Li and ethylene oxide unit was 0.019. The maximum conductivities of Li ions of II and III were in the order of 10-6 and 10-7 S/cm at 30°C, respectively. When the polymers were crosslinked by a hexamethylene residue, the ion conductivities decreased while the degree of crosslinking increased. The temperature dependence of the cation conductivities of these systems could be described by the Williams-Landel-Ferry (WLF) and the Vogel-Tammann-Fulcher (VTF) equation. The results demonstrate that ion movement in these polymers is correlated with the polymer segmental motion. The order of ionic conductivity was K+ 〉 Na+ ≫ Li+. This suggests that steric hindrance and π-electron delocalization of the anions attached to polymer backbone have a large effect on ion-pair separation and their ionic conductivities. Thermogravimetric analysis of the polymers indicated that the degradation temperature for I and II were about 100°C higher than for poly(siloxane-g-ethylene oxide). This is due to the antioxidant properties of sterically hindered phenols and naphthols. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 879-885 
    ISSN: 0887-624X
    Keywords: polyisocyanates ; polymer electrolytes ; metallic cation conducting polymers ; steric hindered phenols ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,6-Di-t-butylphenol and oligo(ethylene oxide) bound covalently to polyisocyanate were synthesized and characterized. The ionic conductivities of their Li, Na, and K phenolates were studied at various temperatures. The conductivities were in the range of 10-7-10-5 S/cm at 30°C. The conductivity of Na and K salts was approximately 102 greater than that of the Li salts. The t-butyl groups serve to dissociate K and Na ions from the phenoxide. The cations, therefore, are more mobile as a result increasing the conductivity. The temperature dependence of ionic conductivity suggests that the migration of ions is controlled by segmental motion of the polymer, shown by linear curves obtained in Vogel-Tammann-Fulchere plots. The polyisocyanate backbone is a rather stiff structure, however, a flexible oligo(ethylene oxide) side chain forms complexes with metal ion. Since the ion transport is associated with the local movement of polymer segments, the rigidity of the polymer backbone does not have much influence on the ion mobility.
    Additional Material: 8 Ill.
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  • 3
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Cephalosporins ; Column switching in HPLC ; On-line plasma sample clean-up
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new high performance liquid chromatographic method was developed using a column-switching technique for the simultaneous determination of cephalexin, cefuroxime, cefoxitin and cephaloridine in plasma. The plasma samples were injected onto a precolumn packed with Corasil RP C18 (37–50 μm) after simple dilution with an internal standard solution in 0.01 M acetate buffer (pH 3.5). Polar plasma components were washed out using 0.01 M acetate buffer (pH 3.5). After valve switching, the concentrated drugs were desorbed in back-flush mode and separated on a Partisil ODS-3 column using acetonitrile in 0.02 M acetate buffer (pH 4.3) (15∶85, v/v) as the mobile phase. The method showed excellent precision with good sensitivity and speed with a detection limit of 0.5 μg/ml. The total analysis time per sample was less than 25 min, and the mean coefficients of variation for intra- and inter-assay were both less than 4.9 %. This method has been successfully applied to plasma from rats after subcutaneous injection of cefuroxime.
    Type of Medium: Electronic Resource
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