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  • Wiley-Blackwell  (45)
  • 1970-1974  (38)
  • 1955-1959  (7)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 237-254 
    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: Changes in the internal morphology of chemically modified lint cotton fibers were investigated by measurement of nitrogen adsorption at liquid nitrogen temperature. Surface areas and pore size distributions were calculated from the adsorption isotherms and compared with findings from measurements of changes in crystallinity and of fibrillar aggregation as shown by electron micrographs. Fibers were either preswollen in water or taken from the rinse water and solvent exchanged through methanol and n-pentane to helium before adsorption measurements were made. Unless reacted in the presence of water, the wrinkle resistance treatments studied caused losses in surface area of 55% or greater. Changes in surface area and porosity of cottons reacted with monofunctional reagents designed to give protective and other types of finishes were dependent on the type of reaction used.
    Additional Material: 11 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 217-236 
    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: Changes in the internal morphology of lint cotton fibers during purification and swelling treatments were investigated by measurement of nitrogen adsorption at liquid nitrogen temperature. Surface areas and pore size distributions were calculated from the adsorption isotherms and compared with findings from measurements of changes in crystallinity and in fibrillar aggregation as shown by electron micrographs. The adsorption measurements were made on fibers which were either preswollen in water or taken from the rinse water after treatment and solvent exchanged through methanol and n-pentane to helium. The large changes found in surface area, pore size distribution, and fibrillar aggregation were accompanied by changes in crystal structure in fibers treated with 5.0M sodium hydroxide. Large changes following treatment with phosphoric acid occurred in pore structure and fibrillar aggregation without concomitant change in crystallinity.
    Additional Material: 12 Ill.
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  • 3
    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.
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  • 4
    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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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 1711-1724 
    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: Recently, the characteristics for pressure corrections in capillary flow have been detailed. The apparent viscosity increases with increasing capillary shear rate for polystyrene and for poly(methyl methacrylate) have been previously explained using free volume theory. These general methods have been developed further in this work and applied to the non-Newtonian flow of a new system, the polycarbonate of bisphenol A. The pressure correction for up to 2 kilobars will be shown to linearize the capillary pressure drop versus the parameter L/D, capillary length over diameter. This correction eliminates the viscosity difference due to variations in L/D ratio. It is also observed that the zero-shear viscosity obtained by the extrapolation of the corrected capillary flow curves agrees well with new and independent data on the same polycarbonate obtained using a Weissenberg rheogoniometer. The flow data have been compared with theories and with earlier published data on the same polymer. The two sets of data are not concordant. These new and corrected shear-dependent data are, however, shown to be expressed qualitatively by the theory of Graessley, using the most probable molecular weight distribution.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 277-287 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studies have been made on the dynamic and steady-shear melt rheology of an ethylene-methacrylic acid copolymer and two of its salts obtained by partial neutralization with sodium and with calcium bases. Measurements were made with a Weissenberg rheogoniometer over a broad range of shear rates and frequency in the temperature interval mainly from 100 to 160°C. The temperature coefficients of dynamic and steady shear viscosity are evaluated at both constant shear rate and constant stress. Likewise, complex dynamic viscosities and apparent high steady-flow viscosities and intercompared at equivalent frequencies and shear rates. The un-ionized acid copolymer shows good correlation between the frequency dependence of the complex viscosity and the shear rate dependence of the apparent viscosity. This is not true for either the sodium salt or the calcium salt. These results are consistent with the two-phase structural model for these materials, i.e., a matrix of hydrocarbon in which are embedded ionic domains.
    Additional Material: 12 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 2697-2706 
    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 survey of viscoelastic data on amorphous polymer melts indicates that the steady-state shear compliance, Je, of many systems can be approximated from a knowledge of their flow response. For systems with monomodel molecular weight distributions, the absolute value of the reduced complex viscosity, η*/η0, is found to equal 0.67 ± 0.03 at the frequency ω, where ωη0Je = 1. This result applies to a variety of polymer systems and to a wide range of molecular weights and distributions as long as the highest molecular weight dispersion of the distribution constitutes more than 20 weight per cent of the sample. This relationship determines Je from non-Newtonian flow data and thus provides a consistent way to relate differently shaped reduced variable curves and to calculate compliances from characteristic times reported in the literature. The connection between some commonly used times and Je is given. The method of calculating Je is successfully applied to capillary measurements of melt viscosities and to characteristic times determined from steady-state shear measurements of concentrated polymer solutions.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 1037-1037 
    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
    Type of Medium: Electronic Resource
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  • 9
    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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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 17 (1971), S. 536-541 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The processes of absorption and desorption with reversible reaction are compared theoretically for reactions of the type A ⇌ nB. With the same concentration difference between bulk and interface, it is found that in general, the rate of desorption is lower than that of absorption. Under certain conditions the difference may be as much as 35%.The analysis is based on the penetration theory. The numerical solution introduces a new transformation of the time and distance variables (based on the error function) which reduces the computing time required. An analytical examination of the penetration theory equations provides an explanation of the results of the numerical solution.
    Additional Material: 6 Ill.
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