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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 41 (1998), S. 8-17 
    ISSN: 0021-9304
    Keywords: AM1 ; molecular orbital models ; zero net shrinkage ; dental restorative ; anhydrides ; maleic ; 4META ; tetrahydrophthalic ; norbornene ; succinic ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The development of a zero net shrinkage dental restorative material based upon a polymer-bioactive-glass composite requires a second-phase material that expands. This study details the mechanisms of organic cyclic anhydride ring expansion via hydrolysis. Six cyclic anhydrides were used to represent potential side groups, each of which could be an expanding phase or component. Maleic, 4META, tetrahydrophthalic, norbornene, itaconic, and succinic anhydrides were modeled using the Austin method (AM1), a semi-empirical molecular orbital method. The reaction pathways were determined for the anhydride ring opening reaction to form an acid for each case. The activation barriers (Ea) for the ring openings were found from the transition state geometries wherein only one imaginary eigen value in the vibration spectrum existed (a true saddle point). In each case the reaction pathway included the hydrogen bonding of a H2O molecule to the ring, weakening of the C—O bridging bonds of the ring, and, finally, the dissociation of the H2O, forming two carboxyl groups and opening the ring. The activation for the ring openings are +34.3, +36.9, +40.6, +43.1, +45.9, and +47.7 kcal/mol, respectively. The volumetric expansion of the anhydrides was estimated based upon the dilation of C—O—C atomic distances. The dimensional change was found to be 24.0%, 24.0%, 19.1%, 20.3%, 20.8%, and 17.9% for the anhydride rings, respectively. Finally, it was found that a linear correlation exists between the cyclic anhydride C—O asymmetric rocking (as-v) vibration and the activation energy (Ea) for hydrolysis to an acid. This may be used as an experimental indicator of a cyclic anhydride's activity. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 41, 8-17, 1998.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 42 (1998), S. 577-586 
    ISSN: 0021-9304
    Keywords: Bioglass® ; HDPE ; composite ; structure and property ; bioactivity ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Particulate 45S5 Bioglass® with an average size of 46 μm was incorporated into a high density polyethylene (HDPE) for potential medical applications. Composites with Bioglass® volumes of 10, 20, and 40% were produced by a manufacturing process consisting of blending, compounding, powdering, and compression molding. The Bioglass® particles were well dispersed, and their homogeneous distribution in the polymer matrix, achieved after compounding, was retained during subsequent composite processing. The Young's modulus and microhardness of the composites increased with an increase in Bioglass® volume while the tensile strength and fracture strain decreased. Fourier transform infrared spectra, obtained from Bioglass®/HDPE samples exposed for 20 h at 37°C to a simulated body fluid (SBF-9), demonstrated that composites of all the compositions examined developed the surface biological apatite layer equivalent to that for bulk Bioglass®. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 42, 577-586, 1998.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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