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  • Tl2Ba2CuO6+δ  (1)
  • polymer dissolution  (1)
  • 1990-1994  (2)
  • 1
    ISSN: 1572-9605
    Keywords: Muon spin rotation ; magnetic penetration depth ; Tl2Ba2CuO6+δ ; overdoped ; pair breaking
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: Abstract We report transverse-field muon-spin-rotation experiments carried out on Tl2Ba2CuO6+δ . This system spans the whole overdoped regime, andT c is reduced by excess oxygen doping, which increases the normal-state carrier concentration. In the heavily overdoped regimeσ(0) is found to scale linearly with the superconducting critical temperatureT c , similar to the behavior previously observed for other cuprates in the underdoped regime. However, for the overdoped region one has to explain the reduction ofσ 0, thus the increase of the magnetic penetration depthλ, in spite of an increasing normal-state carrier concentration. We discuss some possible explanations for this behavior.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 10 (1993), S. 1066-1070 
    ISSN: 1573-904X
    Keywords: hydrocolloid matrix ; zero-order release ; erosion ; polymer dissolution ; relaxation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Matrices are manufactured by direct compression of a powder mixture of a polymer, e.g., methylhydroxypropyl cellulose (MHPC) or polyvinylalcohol (PVAI), and a drug. The following factors that can influence the drug release mode were investigated at constant surface: (i) polymer solution viscosity, glass transition temperature, and swelling; (ii) drug concentration in the matrix and solubility; and (iii) conditions of release experiment (hydrodynamics). In the case of zero-order release profiles (hydrocolloids with low viscosities), only the dissolution of the polymer appears to control the drug release rate. Factors accelerating polymer dissolution resulted in higher release rates. Comparison of swollen and dry hydrocolloid matrices shows that the duration and kinetics of drug release were not controlled by the swelling front moving into the dry polymer, and water penetration and relaxation were not rate controlling. Therefore, the glass transition temperature had no effect on drug release from these hydrocolloids. The higher the hydrodynamic stress exerted on the eroding hydrocolloid, the faster the resulting drug release as a result of accelerated polymer dissolution. With hydrocolloids of very high viscosity the polymer dissolution is slow, and drug relese from the swollen gel appears to be controlled by diffusion according to kinetics of the Higuchi type.
    Type of Medium: Electronic Resource
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