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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 1 (1968), S. 249-254 
    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
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 2132-2139 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The grand canonical Monte Carlo method is used to study a binary mixture of Lennard-Jones atoms confined to a corrugated slit micropore which is in thermodynamic equilibrium with its bulk phase counterpart. The micropore has atomically structured walls; one of the which possesses nanoscale structure in the form of rectilinear grooves (corrugation). The grooved surface divides the confined fluid film into two strip shaped regions, that inside and that outside the grooves. Transverse solidlike order in the film gives rise to shear stress. Transverse order coupled with packing restrictions give rise to a difference between the pore and bulk fluid mixture compositions. Solidlike order may appear within the grooves only, outside the grooves only, or in both regions simultaneously. As the relative alignment of the walls is shifted the pore fluid undergoes freeze–thaw cycles in one or both regions with associated changes in the shear stress and pore fluid composition. The degree of transverse order in the film is less than would be expected in a pure Lennard-Jones film and fluid-solid phase transitions are gradual as opposed to sudden as seen in pure Lennard-Jones films. The magnitude of the shear stress is greatest when a fluid–solid phase transition occurs in both regions of the pore. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2209-2225 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The permeation of benzene and acetone vapors through sulfur-cured natural rubber was studied by the time-lag method. The experimental results were analyzed by a method suggested by Meares. The zero concentration diffusion coefficient D0 was obtained by the early-time method. The Frisch time-lag equation was utilized to estimate both the solubility coefficient s and the additional parameter b required to define the concentration dependence of the diffusion coefficient: D(c) = D0 exp {bc}. This form of concentration dependence was manifested by the corresponding permeability coefficient values. At low entering penetrant pressure, where the transport coefficients are constant, indirect evidence was obtained that D0 is the mechanistically correct diffusion coefficient. The solubility coefficient values calculated for benzene vapor in natural rubber are in reasonable agreement with published equilibrium sorption data for a similar rubber compound. At higher entering penetrant pressures, average diffusion coefficients obtained at steady state tended to be larger than the corresponding average diffusion coefficients derived from the time lags. This same effect has been detected by other experimental approaches. Permeation experiments designed for this rapid method of analysis appear capable of yielding information consistent with that obtained by more time-consuming traditional methods.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 617-624 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This paper details some of the immediate findings for phase morphology formation and persistence in an industrial melt mixing of a polyblend/alloy (‘PB’/‘PBA’). Estimation of the minor phase domain size in a polyblend is feasible if the viscoelasticity functions, interfacial tension of the component-polymers, and the mixing process shear stress level are available. Clusters of domains are formed in the mixer (following streamlines). During steady flow in capillaries the clusters are forming rings which result from the flow velocity profile. Quantitative description of the clusters requires an expansion of image analysis software to account for the interdomain spacing in the clusters, as well as for their pattern. The on-line rheometry was found useful for monitoring coalescence and the effectiveness of the compatibilizer: higher “stiffness” of the PAB melt compared with that of PB shows up in measurements of complex viscosity and modulus. Further study is required, however, for correlating domain spacing and the real time rheometry data (esp. the relaxation spectrum plateau [13]). Finally, the study of phase morphology for the “model” polyblend provides an insight into the melt deformation history in an industrial mixer. It is expected that the distribution of domain sizes would correlate with the pass frequency in the mixing blocks [41], stress distribution in the extruder, and coalescence of the dispersed (“minor”) phase.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyaryloxysilanes was prepared from aromatic diols and dianilino- and diphenoxysilanes. High molecular weight polymers were obtained at temperatures of 200°C. or higher by using melt-polymerization procedures. The polymers, which combine the structures of silicones and polyaromatics, possessed high thermal stabilities and were obtained as materials which (1) failed to melt or soften at 350°C., (2) were gumlike at elevated temperatures, or (3) were soluble, film- and fiber-forming polymers capable of being processed as conventional thermoplastics and having potentially useful mechanical properties. The preparation of monomers, general polymerization procedures, and certain structure-property relationships for the thermoplastic polyaryloxysilanes are considered.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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