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  • Polymer and Materials Science  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 267-275 
    ISSN: 0887-6266
    Keywords: blends ; composition inhomogeneities ; crystallization kinetics ; nucleation ; spherulites ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In polymer blends of an amorphous and a semicrystalline component, the crystallization kinetics and the resulting morphology are heavily determined by the diffusion ability of the whole chains and by the dwelling site of the amorphous polymer. Depending on the relative rates of spherulite growth and chain diffusion, radial composition profiles around the growing spherulites and a gradual increase of the melt bulk composition can develop. The resulting change in composition, particularly at the crystallization front, causes a corresponding temporal variation of the spherulite growth rate. In the present article, two experimental techniques are introduced to prove the existence and to determine the course of these concentration profiles. They are based on the composition dependences of the spherulite growth rate and the number density of primary nuclei. Their efficiency is demonstrated by measurements on PVDF/PEA blends. The blend composition at the crystal growth front was found to change by absolute 25%, and the width of the profile can amount to up to 70 μm. © 1996 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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  • 2
    ISSN: 0887-6266
    Keywords: polymer blends ; crystallization ; diffusion ; composition inhomogeneities ; computer simulation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is well known that crystallization of one component in a polymer blend causes composition profiles around the growing spherulites. Amplitude and width of these profiles, respectively, depend on the ratio between the rates of diffusion and of spherulite growth. They can be determined by suitable experimental means. In the present article, the profiles are modeled, starting from Frank's solution of the diffusion equation in spherical coordinates under the boundary condition of moving walls that simultaneously are sources of the diffusing material. Modeled and experimentally determined profiles in PVDF/PEA and PCL/PS blends agree well. The analysis yields estimates for the diffusion coefficient D in polymeric melts as D ≅ (50··· 500) μm2/h. Finally, the interference of the composition profiles around several adjacent spherulites can be demonstrated. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 40 (1998), S. 324-335 
    ISSN: 0021-9304
    Keywords: titanium ; bioactive coating ; immobilization ; silanization ; covalent attachment ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The surface of implantable biomaterials is in direct contact with the host tissue and plays a critical role in determining biocompatibility. In order to improve the integration of implants, it is desirable to control interfacial reactions such that nonspecific adsorption of proteins is minimized and tissue-healing phenomena can be controlled. In this regard, our goal has been to develop a method to functionalize oxidized titanium surfaces by the covalent immobilization of bioactive organic molecules. Titanium first was chemically treated with a mixture of sulfuric acid and hydrogen peroxide to eliminate surface contaminants and to produce a consistent and reproducible titanium oxide surface layer. An intermediary aminoalkylsilane spacer molecule was then covalently linked to the oxide layer, followed by the covalent binding of either alkaline phosphatase or albumin to the free terminal NH2 groups using glutaraldehyde as a coupling agent. Surface analyses following coating procedures consisted of X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and atomic force microscopy (AFM). Enzymatic activity of coupled alkaline phosphatase was assayed colorimetrically, and surface coverage by bound albumin was evaluated by SEM visualization of colloidal gold immunolabeling. Our results indicate that the linkage of the aminoalkylsilane to the oxidized surface is stable and that bound proteins such alkaline phosphatase and albumin retain their enzymatic activity and antigenicity, respectively. The density of immunolabeling for albumin suggests that the binding and surface coverage obtained is in excess of what would be expected for inducing biological activity. In conclusion, this method offers the possibility of covalently linking selected molecules with known biological activity to oxidized titanium surfaces in order to guide and promote the tissue healing that occurs during implant integration in bone and soft tissues. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 40, 324-335, 1998
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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