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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 6419-6424 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 25 (1991), S. 335-341 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The large difference in reactivity of L-lactide and ε-caprolactone in ring opening polymerization with stannous octoate, leads to the formation of copolymers with blocky structures. By varying the polymerization temperature, copolymers with different average sequence lengths and molecular weights can be synthesized. It is shown that the average monomer sequence length has a large effect on the thermal and mechanical properties of these copolymers.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 26 (1991), S. 71-77 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Two new lactone polymerization catalysts, tin(II)-bis(2,4-pentanedionato-O,O') (Zn(Acac)2) and zinc-bis(2,2-dimethyl-3,5-heptanedionato-O,O') (Zn(DMH)2), together with tin(II)-2-ethylhexanoate (Sn(Oct)2), were used to study the effect of the catalyst in the L-lactide polymerization on the nascent polymer structure. Using Zn(DMH)2 an ultra high crystalline polymer was obtained with a ΔHm of 100 J.g-1. Independent of the catalyst and the crystallinity the structure of the crystalline polymer was a pure α-structure as revealed by WAXS-measurements. SAXS-measurements showed a long period for both the Sn(Oct)2 and the Zn(DMH)2 polymer of about 33 nm., the latter revealing a more complex highly regular structure with up to fourth-order reflections. SEM micrographs showed a fibrillar like structure for the Zn(DMH)2 polymer.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract The infection risk of biomaterial implants is determined by an interplay of bacterial adhesion and surface growth of the adhering organisms. In this study, we compared initial adhesion and surface growth of Pseudomonas aeruginosa AK1 (zeta potential −7 mV) on negatively charged (PMMA/MAA, zeta potential −18 mV) and positively charged (PMMA/TMAEMA-Cl, zeta-potential +12 mV) methacrylate copolymers in situ in a parallel plate flow chamber. Initial adhesion was measured using phosphate-buffered saline and subsequent surface growth of the adhering bacteria using nutrient broth as growth medium. Initial adhesion was twice as fast on the positively charged methacrylate than on the negatively charged copolymer. Surface growth, however, was absent on the positively charged copolymer, while on the negatively charged methacrylate the number of bacteria increased exponentially during surface growth with a generation time of 32 min. From the results of this study it can be concluded that positively charged biomaterial surfaces might show reduced risks of biomaterials-centred infections, despite being more adhesive.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 12 (1993), S. 1048-1051 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 272 (1994), S. 1068-1081 
    ISSN: 1435-1536
    Keywords: Poly(lactide) ; entanglements ; characteristic ratioC ∞ ; hotdrawing ; mechanical properties
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The observed brittle fracture behavior of amorphous polylactides seems to be contradicted by the low value ofC ∞ =2 determined for poly(L-lactide) by Flory and coworkers. Such very flexible polymer chains deform by shear yielding, and fracture in a ductile manner. In this study,C ∞ was estimated in a number of ways, resulting in much higher values ofC ∞ =11.7 andC ∞=9.1 for poly(L-lactide) and L- and D-lactide copolymers, respectively. These high values ofC ∞ and the low entanglement density account for the brittle fracture behavior of amorphous poly(lactide), as well as for the maximum attainable draw ratios of poly(L-lactide) networks and melt spun fibers. Bulk polymerized poly(L-lactide) networks, where crystallization during polymerization impedes severe entangling, could be hot-drawn most effectively to draw ratios of 8–16, resulting in very strong materials with tensile strengths of 550–805 MPa. By comparison, amorphous, non-crystallizable L/D lactide networks, which do not crystallize during polymerization, could be drawn less, to λ=7. These materials with strengths up to 460 MPa could, nevertheless, be oriented much more effectively than linear, amorphous L/D lactide copolymers.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1435-1536
    Keywords: Key words poly(L-lactide) ; hydrolytic degradation ; morphology ; crystallinity ; hot-drawn
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The influence of morpho-logy on the hydrolytic degradation behavior of poly(L-lactide) has been studied. High molecular weight and highly crystalline as-polymerized poly(L-lactide) was obtained in high yields through melt polymerization. Poly(L-lactide) fiber with a draw ratio of 5.6 was obtained by hot-drawing solution-spun fiber. During the bulk degradation of as-polymerized poly(L-lactide), a rapid decrease of molecular weight and tensile properties was observed. This could be explained by the morphology of the material and the presence of thermal stresses and subsequent generation of micro-cracks. The lamellar crystallites in as-polymerized poly(L-lactide) appeared to be very stable towards hydrolysis. The resorption time of high molecular weight as-polymerized poly(L-lactide) in vivo was estimated at 40–50 yr by extrapolation of molecular weight data. Hot-drawn poly(L-lactide) fiber showed exceptional hydrolytic stability under a static load and substantially retained its mechanical properties over a period of more than 5 yr. The high perfection of the crystalline fiber and the elimination of micro-voids obtained by hot-drawing prevented penetration of water and induced surface erosion of the fiber.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 32 (1994), S. 509-515 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Recent studies have indicated that complications like swelling and inflammation of the surrounding tissue may occur in the late stage of thein vivo degradation of semi-crystalline PLLA bone fixation devices. Incorporation of an anti-inflammatory drug, like a salicylate, in the poly(L-lactide) chain might be a route to prevent these complications. In this study, it has been shown that it is possible to copolymerize L-lactide with di- and trisalicylide and to use salicylic acid as an initiator for the L-lactide polymerization or the L-lactide/ε-caprolactone copolymerization. Furthermore, PLLA was blended with poly(salicylic acid) and Zn(salicylate)2 was synthesized and turned out to be a catalyst for the ring opening polymerization of L-lactide. The binary poly(L-lactide)/o-acetyl salicylic acid system has an eutectic composition for 52 % w/w of poly(L-lactide) in the mixture. Its eutectic melting temperature is 119 °C.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 29 (1992), S. 571-578 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary As-polymerized poly(L-lactide), (PLLA), has a much higher impact strength than after compression moulding. Several routes have been explored to further increase the impact strength of nascent PLLA. First results on the preparation of composites with carbon fibres, the copolymerization with trimethylene carbonate and ε-caprolactone, the block copolymerization with rubbers and the plasticization with ethyl acetate indicate possibilities to prepare much more impact resistant as-polymerized PLLA materials.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary High molecular weight copolymers of L-lactide and ε-caprolactone have been synthesized by ring opening copolymerization with stannous octoate as catalyst. The good mechanical properties of the 50/50 copolymers make it a suitable material for biomedical applications such as nerve guides etc., where degradation of the elastomeric implant is required. In contrast to the frequently used MDI containing polyurethanes, degradation products of the P(LLA-ε-CL) are non toxic. The use of such a material is therefore preferable.
    Type of Medium: Electronic Resource
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