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  • 11
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 519-536 
    ISSN: 0887-6266
    Keywords: poly[1-(trimethylsilyl)-1-propyne] ; Monte Carlo simulation ; diffusion coefficient ; molecular dynamics ; gas solubility ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The bonded constants in the DREIDING force field have been parameterized for poly[1-(trimethylsilyl)-1-propyne] (PTMSP) from AM1 calculations of the dimer. The resultant force field has been validated through the simulation of amorphous cell density and x-ray data (d-spacing) and used to obtain diffusion coefficients for five gases (He, O2, N2, CH4, and CO2) from 0.5 ns NVT molecular dynamics using the Einstein relationship. In addition, solubility coefficients of these gases have been obtained from the particle insertion method of Bezus et al. and from a fixed-pressure Monte Carlo method which was also used to calculate sorption isotherms. In general, there is good to excellent agreement between experimental and simulated values of the diffusion and solubility coefficients for He, O2, N2, and CH4. Sorption isotherms and dual-mode parameters calculated from the simulation results for O2, N2, and CH4 agree very favorably with experimental data (no experimental data was available for He). In the case of CO2, diffusion and solubility coefficients as well as sorption isotherms are underestimated. The less satisfactory results for CO2 have been tentatively attributed to inadequacy of the generic nonbonded Lennard-Jones potential terms of DREIDING used in this study. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 519-536, 1998
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 1048-1054 
    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: Blends of poly(2,6-dimethyl-1,4-phenylene oxide) (PMMPO) and poly(4-methylstyrene) (P4MS) were found to be compatible from a variety of experimental methods including calorimetric, density, and mechanical property measurements. Blend property behavior was similar to that widely reported for PMMPO/polystyrene (PS) blends. For each blend composition studied, a single glass transition temperature (Tg) was detected by differential scanning calorimetry. The compositional dependence of blend Tg was equally well represented by the empirical inverse rule of mixtures or by the Couchman thermodynamic expression. Density measurements of molded films suggested a mild excess volume of mixing that was slightly smaller than that observed for blends of PMMPO and PS. As in the case for PMMPO/PS, densification in the solid state may be associated with the observed mechanical property behavior of the PMMPO/P4MS blends. Initial modulus at each blend composition was larger than would be predicted by a simple weighted average of component polymer values. Tensile deformation changed from a ductile to a brittle mode of failure with increasing P4MS composition. The yield stress for ductile compositions and ultimate stress of brittle samples were both higher than found for the corresponding unblended polymers and higher than would be predicted from a simple additive relationship of weighted component properties. Blend impact strength determined by small strain rate tensile tests rapidly decreased to low levels with increasing P4MS composition. This drop in impact strength became more composition sensitive at higher loading rates during multiaxial deformation in an instrumented dart impact tester.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 28 (1990), S. 7-12 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 1123-1131 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: FTIR spectra of cellulose acetate (CA) and poly(methyl methacrylate) (PMMA) at 35°C have been obtained as a function of carbon dioxide pressure at pressures up to 55 atm in a specially designed FTIR cell. Results indicate that the carbonyl stretching vibrations for CA (1752 cm-1) and PMMA (1731 cm-1) shift to slightly higher wave numbers with increasing pressure. The small shifts suggest dipole-dipole interactions between CO2 and the carbonyl group. In both cases, the shift appears to be linear with pressure. This linearity is interpreted in the framework of the dualmode theory to suggest that gas-polymer interactions occur in the Henry's law dissolution mode.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 15
    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: Blends of poly(2,6-dimethyl-l,4-phenylene oxide) and copolymers of styrene and maleic anhydride have been characterized by differential scanning calorimetry, dynamic mechanical analysis, and tensile measurements. Differential scanning calorimetry measurements indicate a single broadened glass transition for each blend of a 8 wt.% maleic anhydride copolymer, P(S-8MA), but two glass transitions when the copolymer composition is 14 wt.% MA, P(S-14MA). The glass transition temperatures of the former blends follow a sigmoidal dependence on blend composition, which is explained on the basis of evidence for phase separation from their dynamic mechanical tan 8 spectra. Tensile moduli of both blends reach a maximum at intermediate blend compositions; however, large-strain mechanical properties are highly dependent on blend compatibility and the method of sample preparation. The more homogeneous P(S-8MA) blends yield at low-to-intermediate copolymer compositions but fail in a brittle mode at higher compositions. All heterogeneous P(S-14MA) blends undergo brittle failure, but comparison of experimetal values of ultimate stress and strain with predictions from empirical relationships developed for composites indicate that interfacial adhesion is strong in these systems.
    Additional Material: 28 Ill.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 22 (1982), S. 653-653 
    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
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 3381-3383 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 20 (1982), S. 381-383 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 20 (1982), S. 495-500 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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