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  • Articles  (939)
  • Polymer and Materials Science  (939)
  • Wiley-Blackwell  (939)
  • American Association for the Advancement of Science
  • American Meteorological Society
  • Blackwell Publishing Ltd
  • Springer Nature
  • Springer Science + Business Media
  • 1960-1964  (939)
  • 1964  (939)
  • Physics  (939)
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  • Articles  (939)
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  • Wiley-Blackwell  (939)
  • American Association for the Advancement of Science
  • American Meteorological Society
  • Blackwell Publishing Ltd
  • Springer Nature
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  • 1960-1964  (939)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1919-1919 
    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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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1903-1918 
    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 rate of crosslinking of concentrated gelatin solutions in water has been measured by means of a gelation timer. Some effects of temperature, pH, crosslinking agent, and gelatin concentration have been measured. The crosslinking agents have varied from fast-acting chrome alum, glutaraldehyde, and a carbodiimide to slow-acting mucobromic acid and dialdehyde starches. Detailed crosslinking mechanisms are discussed for dimethylol urea, mucobromic acid, and several dialdehyde crosslinking agents. Some effects of urea and other additives on the dimethylol urea crosslinking rate are described.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1921-1939 
    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 new method of curing phenolic novolac resins by means of cyclic formals under the catalytic influence of strong acids is given. It was proved that the formals react with the novolac molecules to form a highly crosslinked resite structure. As a practical consequence of this novel curing process it is possible to use the new resins at low or contact pressures in molding operations. The physical properties of the end products in general resemble those of the standard phenolic casting resins.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1941-1947 
    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 analysis of a stationary, rotationally symmetric liquid jet which leads to an expression for the average normal stress at the exit of a capillary tube is reexamined with particular attention to the effect of surface tension. The limiting case of a nearly cylindrical jet is compared with the analysis presented by Gavis and Middleman.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1889-1901 
    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 relationship between biaxial stress-rupture behavior and polymer morphology has been investigated for a series of compression-molded disks of linear polyethylene. Rupture data were obtained over a range of temperatures on polymers of several melt indices that had been solidified at two rates. Two failure mechanisms were observed: one at high stress levels, which was ductile; the other at low stress levels, which was brittle. The stress level at which the mechanism changed from ductile to brittle decreased as the measurement temperature increased, as the melt index of the polymer increased, and as the rate or solidification decreased. It was shown that initial pressurization of the disks causes the formation of microscopic surface fissures along spherulite boundaries as well as within individual spherulites. The extensive growth of these fissures at high stress levels sufficiently raises the stress on the sound portions of the polymer to cause large-scale macroscopic drawing of the spherulites. At low stress levels the initially formed fissures grow by a localized drawing process at their ends. A macroscopic crack forms by a chance coalescence of a number of individually growing fissures. This process is more rapid in disks of polymer that form large spherulites when cooled slowly from the melt. The spherulite size in disks of polymer of low melt index is much smaller under the same conditions of cooling and is less sensitive to the cooling rate than in disks of polymer of high melt index. Annealing of rapidly cooled disks whose microstructure contains relatively small spherulites reduces the stress at which the failure mechanism changes without appreciably altering the spherulite size. Oxidation of the polymer also reduces the transition stress.
    Additional Material: 10 Ill.
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  • 6
    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: Many derivatives of phenyl salicylate turn yellow when they are exposed, in solution, to ultraviolet light. This limits their usefulness as ultraviolet stabilizers for plastics. Evidence is presented to support the postulation that the yellowing is due to the formation, by a photochemical ortho rearrangement, of a derivative of 2,2′-dihydroxybenzo-phenone. Aromatic salicylates, such as 2,6-dialkylphenyl salicylate, in which the ortho rearrangement is blocked, are found to be nonyellowing stabilizers, although less effective than the better yellowing varieties, such as p-octylphenyl salicylate. Loss of stabilizer by volatilization, either in compounding or during subsequent exposure, is shown to be an important factor in limiting the effective performance of the stabilizer.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1985-1989 
    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 new method for hydroxyl analysis is described in which excess toluene diisocyanate is reacted with a hydroxy compound, preferably in the presence of a catalyst, and the unreacted isocyanate is determined with dibutylamine reagent. The method is particularly applicable to polyethers intended for urethane foam preparation. It is rapid, is accurate, and has the added advantage of including such impurities as would be expected to consume isocyanate during a foam preparation.
    Additional Material: 1 Tab.
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  • 8
    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: Determinations of the degree of chemical crosslinking and crosslinking efficiency values E (i.e., the number of sulfur atoms combined in the network per chemical crosslink present) have been used in conjunction with the chemical probes triphenylphosphine and sodium di-n-butyl phosphite to establish the structural features of sulfur links in vulcanizate networks derived from a variety of accelerated natural rubber-sulfur systems, from a cis-1,4-polyisoprene-TMTD-zinc oxide system, and from natural rubber and ethylene-propylene rubber crosslinked with a dicumyl peroxide-sulfur system. The triphenylphosphine converts polysulfide links into monosulfide and, to a lesser extent, disulfide links. The values of E′, i.e., the number of sulfur atoms combined in the network per chemical crosslink present after triphenylphosphine treatment are, therefore, a measure of the extent of main-chain modification in the network by cyclic monosulfide groups and/or pendant groups of the type: —Sx—Accel. (where x ≥ 1 and Accel. is an accelerator fragment). Sodium di-n-butyl phosphite cleaves di- and polysulfide crosslinks but leaves monosulfide and carbon-carbon crosslinks intact, and thus determination of the degree of chemical crosslinking before and after treatment with this reagent yields estimates of these two different classes of crosslinks. The combined results indicate that the efficiency of utilizing sulfur for crosslinking and, therefore, the structural complexity of the derived networks are very sensitive to the nature of the vulcanizing system (type and relative concentrations of crosslinking agent, accelerator, and activator) and vulcanizing conditions (time and temperature of cure). In general, the proportion of crosslinks which are di- and/or polysulfidic decreases with increasing cure time, and for the accelerated sulfur systems the structural complexity of the network increases with cure time, especially at higher vulcanizing temperatures and with low concentrations of fatty acid activator.
    Additional Material: 9 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 2049-2065 
    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: Small particles (ca. 700 A.) in an SB-R latex can be agglomerated (aggregation and coalescence) to the large size and heterogeneous distribution required for fluid high solids latex. This agglomeration is promoted by high molecular weight materials such as polyvinyl methyl ether (PVM). The mechanism of this agglomeration has been investigated. The effects of controlled variations in the amounts of PVM, electrolyte, soap and latex solids content were determined using statistically designed experiments. The agglomeration was found to differ from Smoluchowski kinetics in that it could best be described by the relationship: (1/n) = (1/n0) + at - bt2 where n = particle number, t = time and a and b are constants. The agglomeration rates were about 1011 to 1012 times slower than the theoretical Smoluchowski rapid coagulation rate. Increases in PVM, soap, and latex solids increased the agglomeration rate. The agglomerations were self-limiting and reached equilibria the level of which increased with increases in PVM and decreased with increases in soap. Regression equations relating the effects of the controlled variables on the agglomeration rate and the equilibria states are derived and presented graphically. The particle size distribution of the final latex was significantly correlated, with that expected from theoretical collision theory.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 2029-2048 
    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. new theory for the acid-base properties of fibers is presented, resembling those for polyelectrolytes, and based on the normal titration of the charged groups of the fibers and the energy needed to remove the protons from the fiber to the solution, against the electrostatic, osmotic, and affinity differences. The acid titration equation for a poly-ampholyte fiber is: \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm pH} = {\rm p}K_0 ^\prime - \log [{{\left( {1 - \alpha } \right)} \mathord{\left/ {\vphantom {{\left( {1 - \alpha } \right)} \alpha }} \right. \kern-\nulldelimiterspace} \alpha }] - \left( {{{0.4343} \mathord{\left/ {\vphantom {{0.4343} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right)[\chi F + \tau \bar V_{\rm H} + \Delta \mu _{\rm H}^{\rm o} ] $\end{document} where pK0′ is the intrinsic dissociation constant of the titration groups in the fiber, α is the degree of dissociation, χ is the electrostatic potential of the fiber, τ the osmotic pressure, V̄H the partial molar volume of the hydrogen ion, and ΔμHo the difference of standard chemical potential in the fiber and the solution. In all cases examined, the osmotic term proved to be negligible. The electrostatic potential was calculated as suming it to be uniform over the fiber. For wool, pK0′ is independent of salt concentration but varies linearly with degree of dissociation, indicating that two pK's are operating, pKq = 3.585 for paired groups and pKp = 4.855 for nonpaired groups at 0°C., present in equal proportions. Titrations of wool with sulfuric acid and a wide range of strong monobasic acids also obey the theory, and values of the anion affinities in general agreement with those given by Gilbert and Rideal are found. The acid titration of native ox-hide collagen gave a constant value of pK0′ = 4.0. For nylon, the value of pK0′ is, to a first approximation, independent of degree of dissociation and salt concentration, in agreement with the theory.
    Additional Material: 4 Ill.
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