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  • Polymer and Materials Science  (4)
  • GENERAL  (1)
  • Physics  (1)
  • 1970-1974  (5)
  • 1965-1969
  • 1973  (5)
Collection
Publisher
Years
  • 1970-1974  (5)
  • 1965-1969
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 605-618 
    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: A theoretical model for drying of a thin gel film is presented. The model is based upon the premise that as solvent is removed from any portion of a gel structure which is permeable by the solvent, the structure shrinks locally to fill the voids left by the solvent. The diffusion coefficient of solvent through the gel film is assumed to be an exponential function of concentration and temperature. The governing equations for the model indicate that for nonisothermal drying, the results of drying and shrinkage rates are functions of 13 independent dimensionless system variables. These results are obtained with the help of a computer solution of the proposed model. The computer results indicate that, except under extreme temperature conditions, the drying and shrinkage rates are most influenced by dimensionless groups M, P, and P̄, defined by eq. (9) of the paper. Furthermore, the drying and shrinkage rates are essentially independent of groups M and P for the values of M and P greater than approximately 100 and 10, respectively. The effect of variable solvent diffusivity on approximate time to achieve the steady-state drying and shrinkage rates is approximately handled by defining a dimensionless time variable τ in terms of average solvent diffusivity. Finally, some experimental data on drying and shrinkage rates of isothermal drying of lyphogel film under natural convection condition are obtained. These data are found to be in qualitative agreement with similar computer predictions by the proposed model.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 3509-3514 
    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: The glass transition temperatures of the poly(alkyl α-cyanocrylates) were determined by the dilatometric technique, and some of the values were checked by differential thermal analysis. The data indicate that the Tg's appear to decrease with increase in the size of the alkyl group, for a given molecular weight range. It was also found that the Tg of poly(methyl or butyl α-cyanoacrylate) increased with molecular weight. All cyanoacrylates, excepting methyl and ethyl esters, formed only low molecular weight polymers in aqueous surroundings. Therefore, they have characteristic low glass transition temperatures, causing coalescence at low temperatures.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 2761-2770 
    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: The nature and magnitude of mechanical reactions of polystyrene in capillary flow has been examined in a model extrusion process. Studies on polystyrene quantify the sensitive increase in shear degradation tendency with increasing polymer molecular weight. A molecular weight spectrum caused by the shear stress profile was measured across the extrudate radius by the new technique of solvent coring. It was further determined that an appreciable fraction of the mechanical reaction is shear induced in the capillary reservoir. This is confirmed by precision determinations of molecular weights and distributions by gel permeation chromatography on samples taken from concentric layers in the capillary reservoir after 50% sample extrusion. These results, involving traces of oxygen as a chemical probe, describe the stress profile in the reservoir and in the capillary during the pressure extrusion of high molecular weight polystyrene. Thus, changes in molecular weight and distribution may be attributable to changes in different portions of the shear geometry rather than the uniform changes generally considered. Clear evidence is also presented showing the dramatic effects of oxygen on these shear-induced changes in molecular weight and distribution.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2001-2012 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polarized infrared absorption spectra have been obtained by Fourier-transform spectroscopy for several crystalline and noncrystalline absorption bands of polyethylene crystallized by orientation and pressure in capillary viscometer. An analysis of data obtained at room temperature yielded degrees of crystallinity which are in good accord with values obtained from calorimetry and density measurements. The dichroism of the infrared absorption bands for the crystalline region revealed an extreme degree of orientation consistent with previous x-ray studies and also demonstrated that the degree of orientation is a good or better than that obtained from drawn polyethylene films with extension ratios of 20. Dichroism of bands from the amorphous phases revealed that the noncrystalline chain segments are in a comparatively relaxed state compared with results for drawn films having extension ratios of about 2 to 7. This is 1/10 to 1/3 the extension ratio of drawn polyethylene which shows maximum crystalline orientation. The results also indicated that the ratio of the GTG′ to GG segment conformations in the amorphous regions is larger than that of amorphous portions in unoriented polyethylene. The vinyl endgroups were shown to be highly oriented, while the main bulk of the amorphous polymer was fairly relaxed, i.e., of low orientation. It is concluded that the amorphous polyethylene state is strongly dependent on the nature of the crystalline-amorphous interface.
    Additional Material: 1 Ill.
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  • 5
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    In:  CASI
    Publication Date: 2005-08-31
    Keywords: GENERAL
    Type: Ann. Progr. Rev.; 5 p
    Format: text
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