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  • Chemical Engineering  (5)
  • diffusion-limited reaction  (1)
  • glass transition temperature  (1)
  • 1
    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
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    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: Tensile, cyclic, and tear properties were compared for several styrene-butadiene-styrene (SBS) triblock copolymers, KRATON D2104, D1101 and D1102, and blends of D2104 with monodisperse polystyrene of various molecular weights. D2104 is expected to have a morphology of polystyrene spheres in a polybutadiene continuous matrix. The mechanical properties of D2104 were compared to the properties of SBS materials which have higher styrene contents and exhibit cylindrical or lamellar morphologies. Blending the D2104 with polystyrene (molecular weights ranging from 2000 to 51,000) to 24 and 28 wt % total styrene content showed that the tensile strength obtained for a blend was dependent on the molecular weight of the polystyrene added. Cycle testing of the D2104-polystyrene blends showed that with increasing polystyrene content the softening effect increases with increasing strain. This indicates that the degree of phase continuity of the polystyrene domains may be changing from a spherical morphology to a cylindrical morphology similar to that of pure SBS with 28 wt % styrene content. Tear test results for the blends were also observed to be similar to the results for pure SBS of the same total polystyrene content.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 42 (1996), S. 1157-1163 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2999-3008 
    ISSN: 0887-6266
    Keywords: chain length effects ; diffusion-limited reaction ; polymer solution ; phosphorescence quenching ; segmental diffusion ; polymer-polymer reactions ; reaction kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Model interactions have been studied by phosphorescence quenching to obtain a better understanding of the chain length dependence of interpolymeric chain end-chain end reactions such as those involved in the termination step of free radical polymerization. For small molecule-polymer interactions in dilute cyclohexane solution, quenching rate constant (kq) data agree with the Smoluchowski equation prediction that kq scales as polymer molecular weight (MW) to the -½ power, confirming self-diffusion control. For polymer-polymer interactions in dilute solution, the chain length dependence is weaker than that predicted by translational diffusion control, as described by the Smoluchowski equation, but is stronger than that predicted by renormalization group theory. For interactions between 70000 MW benzil-end-labeled polystyrene and varying MWs of anthracene-end-labeled polystyrene at 300 g/L polymer, kq decreases by a factor of 10 in going from MWs of 100 to 1000 g/mol; beyond 1000 g/mol, kq is nearly independent of chain length. Such effects indicate that the importance of oligomeric radical self-diffusion and polymer radical chain-end segmental mobility must be carefully considered in understanding the termination process in free radical polymerization. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2987-2997 
    ISSN: 0887-6266
    Keywords: small molecule diffusion ; fluorescence nonradiative energy transfer ; glass transition temperature ; rubbery polymer ; probe shape effects ; probe flexibility effects ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel experimental approach involving fluorescence nonradiative energy transfer (NRET) is employed to study the Fickian diffusion of small molecules in rubbery poly(isobutyl methacrylate) (PiBMA) films near the glass transition, using a formalism that directly relates the small molecule translational diffusion coefficient, D, to changes in the normalized nonradiative energy transfer efficiency, EN. Values of D for pyrene, 1,3-bis-(1-pyrene) propane (BPP), 1,3-bis-(1-pyrene) decane (BPD), 9,10-bis-phenyl ethynyl anthracene (BPEA), diphenyl Disperse Red 4 (DPDR4), and decacyclene in PiBMA are measured over temperatures ranging from approximately Tg to Tg + 25°C. Among these chromophores, significant differences in both the magnitude and temperature dependence of D are observed which are attributed to differences in molecule shape and flexibility, as well as molar volume. Other factors being equal, chromophore flexibility was shown both to increase the magnitude of D and to decrease its dependence on temperature, as does an increase in aspect ratio. For BPD, these effects are attributed to the ability of the flexible molecule to diffuse in a piecewise manner, requiring the cooperative mobility of fewer polymer chain segments than a rigid molecule of the same molar volume. For BPEA and DPDR4, this deviation from D being dominated by molar volume effects is attributed the to high aspect ratio of these elongated molecules. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 644-653 
    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
    Notes: The influence of polymer molecular weight, molecular weight distribution, and polymer-solvent interactions on the thickness and topography of spin-coated polymer films was examined. For films prepared from dilute solutions, highly volatile solvents or fair or “poor” solvents for the polymer adversely affect film surfaces causing nonuniformities (waves) to appear. However, if the concentration of these solutions is increased to approximately the concentration at which entanglements are formed, nearly uniform films are produced even if the solvent employed is highly volatile, such as dichloromethane. When toluene is employed as the solvent, which has a relatively low volatility and therefore forms nearly flat film surfaces, films prepared from dilute solution were found to have thicknesses, h, proportional to ηo0.34 Ω-0.49 for polystyrene and ηo-0.39 Ω-0.49 for poly(methylmethacrylate) where ηo is the zero-shear rate solution viscosity and Ω is the rotational speed at which the films were prepared. These results suggest that the exponents associated with ηo and Ω may be nearly independent of the type of polymer used as long as flat films are produced. Finally, the molecular weight parameter most important in controlling final film thickness for films made from dilute solutions is Mv, the viscosity-average molecular weight.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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