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  • 1
    Online Resource
    Online Resource
    American Chemical Society (ACS) ; 1998
    In:  Macromolecules Vol. 31, No. 1 ( 1998-01-01), p. 193-200
    In: Macromolecules, American Chemical Society (ACS), Vol. 31, No. 1 ( 1998-01-01), p. 193-200
    Type of Medium: Online Resource
    ISSN: 0024-9297 , 1520-5835
    RVK:
    Language: English
    Publisher: American Chemical Society (ACS)
    Publication Date: 1998
    detail.hit.zdb_id: 1491942-4
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  • 2
    Online Resource
    Online Resource
    Society of Rheology ; 1999
    In:  Journal of Rheology Vol. 43, No. 5 ( 1999-09-01), p. 1141-1155
    In: Journal of Rheology, Society of Rheology, Vol. 43, No. 5 ( 1999-09-01), p. 1141-1155
    Abstract: Poly(lactic acids) (PLAs) are a family of polyesters available via fermentation from renewable resources and are the subject of considerable recent commercial attention. In this study, the melt rheological properties of a family of poly(lactic acid) stars are investigated and compared to the properties of the linear material. For polymers made from a 98:2 ratio of the L to D enantiomeric monomers it is found that the entanglement molecular weight is in the range of 9000 g per mole (Me≈8700 g/mol) while the molecular weight for branch entanglement is inferred to be approximately 3500 g per mole (Mb≈34 600 g/mol). In addition, the zero shear viscosity of the linear material increases with the 4.6 power of molecular weight. These results may suggest that PLA is a semistiff polymer in accordance with other recent findings. The increase in zero shear viscosity for the branched materials is measured and quantified in terms of appropriate enhancement factors. Relaxation spectra show that the transition zone for the linear and branched materials are nearly indistinguishable, while the star polymers have greater contributions to the terminal regime. The effects of chain architecture on the flow activation are found to be modest, implying that small scale motions in PLA homopolymers largely control this phenomenon. Good agreement is found between the dynamic data and many aspects of the theory of star polymers, however, a dependence of the zero shear viscosity on the number of arms is observed.
    Type of Medium: Online Resource
    ISSN: 0148-6055 , 1520-8516
    Language: English
    Publisher: Society of Rheology
    Publication Date: 1999
    detail.hit.zdb_id: 1461060-7
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1997
    In:  Journal of environmental polymer degradation Vol. 5, No. 3 ( 1997-07), p. 125-136
    In: Journal of environmental polymer degradation, Springer Science and Business Media LLC, Vol. 5, No. 3 ( 1997-07), p. 125-136
    Type of Medium: Online Resource
    ISSN: 1064-7546
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1997
    detail.hit.zdb_id: 2017207-2
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  • 4
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1995
    In:  MRS Proceedings Vol. 385 ( 1995)
    In: MRS Proceedings, Springer Science and Business Media LLC, Vol. 385 ( 1995)
    Abstract: Improving the processing and formability of ceramic components prior to firing (as green bodies) requires an enhanced understanding of how the polymeric binder components function. We report on the role of surface energetics on the structure of the copolymeric monolayers formed via adsorption from solution. Also, results on the effects of surface energetics on the kinetics of the adsorption are reported. A silicon wafer with an oxide layer is used as the surface and adsorption takes place from toluene. Surface energetics are varied by treatment of the oxide surface with a series of silane coupling agents which contain either amine, epoxide, or vinyl functional groups. The block copolymers used consist of relatively short poly(ethylene oxide) (PEO) blocks and much longer polystyrene (PS) blocks. Ellipsometry is used to determine the grafting density, σ (chains/nm 2 ), and Fourier Transform Infrared spectroscopy is used to investigate the copolymer on the surface. It is seen that the time required to reach equilibrium increases as the strength of the interaction between the copolymer and the surface increases. Also, the diblock copolymers appear to obey the scaling laws proposed by Marques and Joanny on all the surfaces studied. ( i.e., σ ∝ 1/N A , when the copolymer is symmetric or moderately symmetric and σ ∝ 1/β 2 , when the copolymers are asymmetric, where N A is the number of segments of the adsorbing block and β is the ratio of the size of the nonadsorbing block to that of the adsorbing block.)
    Type of Medium: Online Resource
    ISSN: 0272-9172 , 1946-4274
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1995
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  • 5
    Online Resource
    Online Resource
    Elsevier BV ; 1995
    In:  Fluid Phase Equilibria Vol. 109, No. 2 ( 1995-8), p. 157-169
    In: Fluid Phase Equilibria, Elsevier BV, Vol. 109, No. 2 ( 1995-8), p. 157-169
    Type of Medium: Online Resource
    ISSN: 0378-3812
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1995
    detail.hit.zdb_id: 1483573-3
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