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  • 1
    Electronic Resource
    Electronic Resource
    Polyurethane elastomers from post-grafted polymer-polyol systems (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 133-136 
    Details
    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: Certain homopolymer-polyol mixtures, after treatment with a free-radical generating agent or ionizing radiation, will produce polyurethane elastomers of nearly twice the stiffness and tensile properties compared to control elastomers made with untreated mixtures. Specific examples of these mixtures include the homopolymers of acrylonitrile and vinyl chloride with a poly(oxypropyl) triol of about 3000 molecular weight as the polyol in each case. The marked improvement in the stiffness and tensile properties of elastomers made with the treated mixtures over those of the untreated controls indicates a grafting process occurring between the polyol and homopolymer upon the generation of free radicals. In the present work, grafting could occur by a chain-transfer hydrogen-abstraction mechanism, whereby a free-radical site is generated on both the homopolymer and polyol chains. Coupling of these two free-radical sites would thus result in the establishment of a polymer-polyol graft bond.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110111
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  • 2
    Electronic Resource
    Electronic Resource
    Graft copolymerization of vinyl monomers in wool fibers (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 115-126 
    Details
    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: Graft copolymerization of vinyl monomers, mainly methyl methacrylate, in reduced, successively alkylated, or KCN-Treated wool fibers was performed in the redox LiBr-persulfate system without homopolymer. The reduction gives a striking effect in promoting the graft copolymerization. Methylation or ethylene recrosslinking of the reduced wool, especially the former, decreases the graft-on remarkably. By the KCN treatment in which the conversion of disulfide to lanthionine bonds occurs, the grafting is decreased in the bromide-persulfate system but promoted in the system with persulfate alone. Methylation or KCN treatment of wool as well as reduction brings about a great increase in the absorption of persulfate. The grafting of the lanthionine-containing wool in the redox system accompanied by the liberation of bromine might be retarded by the pronounced bromination of monomers over the inhibiting of homopolymerization, because the lanthionine bonds are more stable to bromine than the disulfide bonds. In general, disulfide bonds and the other easily oxidized components of wool may perhaps play an important role in regulating the bromination of monomers and in the graft copolymerization without homopolymer. The molecular weight of graft polymer is decreased distinctly with increasing extent of reduction of wool. From these results, the thiol groups on wool are considered to give predominantly graft centers by the radicalotropy from SO4-·, OH·, and/or Br·.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110109
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  • 3
    Electronic Resource
    Electronic Resource
    Plastic Materials. J. A. Brydson. Van Nostrand Co., Inc., Princeton, New Jersey, 1966. x + 576. $18.50 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 153-153 
    Details
    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
    URL: http://dx.doi.org/10.1002/app.1967.070110115
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  • 4
    Electronic Resource
    Electronic Resource
    Some mechanical properties of an epoxy resin system cured with multiple crosslinking agentsProd. No. 1445 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 171-177 
    Details
    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: Arbitrary cure times and glass transition temperatures are reported for an epoxy resin cocrosslinked by various weight fractions of hexamethylenediamine (HMDA) and m-phenylenediamine (m-PLDA). The glass transition temperatures of the epoxy resin systems studied yielded an excellent fit to an empirical equation developed by Dyvik for copolymers. The cure time parameters were found to be a linear function of the weight fractions of each crosslinking agent present. The mechanical properties of the epoxy resins were measured by an in situ dynamic modulus technique which employed the use of a resin-coated metallic substrate.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110202
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  • 5
    Electronic Resource
    Electronic Resource
    Antiplasticization. III. Characteristics and properties of antiplasticizable polymersPaper presented at the 152nd National Meeting of the American Chemical Society, New York, September 1966.Prod. No. 1451 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 227-244 
    Details
    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: Antiplasticization is applicable to polymers which contain rigid, polar groups and stiff chains, such as many bisphenol polycarbonates and polyesters, 2,2,4,4-tetramethyl-1,3-cyclobutanediol polycarbonates and polyesters, cellulose triacetate, and a commercial poly(sulfone ether). The stiffness, hardness, and tensile strength of these polymers are increased by antiplasticizers, and the elongation, impact strength, and heat-distortion temperature are decreased. The stiffness of antiplasticized polymers can be further increased by crystallization. A clear, hard, stiff, tough, self-extinguishing molding plastic with good electrical properties and improved resistance to stress cracking is obtained by antiplasticizing bisphenol A polycarbonate with 20% Aroclor 5460.
    Additional Material: 9 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110206
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  • 6
    Electronic Resource
    Electronic Resource
    Resistance of Valonia cellulose to mercerizationProd. No. 1456 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 289-296 
    Details
    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 mercerization behavior at 20°C. of Valonia macrophysa cellulose of Japanese origin was investigated by x-ray, moisture regain, and infrared spectrographic methods. The NaOH concentration range necessary for mercerization was 16-20%, which is higher than those required for wood pulp (8-11%), ramie or cotton (11-14%), and even the animal cellulose, Tunicin (14-16%). Treatment with the alkaline solution of the ordinary concentration (17.5%) for 4 days could not mercerize it, and even mercerization with a 19% solution brought about the presence of the reflection from (101)II along with those from (101)I and (101)I after regeneration. Such a high resistance to mercerization of the Valonia cellulose may be due to its larger crystallite size rather than the crystalline content.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110209
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  • 7
    Electronic Resource
    Electronic Resource
    Elastomer processing and application of rheological fundamentalsProd. No. 1452 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 321-334 
    Details
    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: Elastomer processing operations are discussed and classified as unit operations. The theory of nonlinear viscoelasticity is applied to processing unvulcanized amorphous rubber and the significance of the maximum relaxation time τm is emphasized.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110301
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  • 8
    Electronic Resource
    Electronic Resource
    Polymer degradation. V. Changes in molecular weight distributions during sonic irradiation of polyisobuteneProd. No. 1470 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 335-340 
    Details
    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: Gel permeation chromatography was used to follow changes in the molecular weight distribution of a polyisobutene, initial Mv = 466,000, during degradation induced by sonic irradiation. Seven samples taken at times of 200-163,500 sec. were studied. In general, a steady decrease in molecular weight was observed, although a bimodal distribution was present after 20,000 sec. irradiation. Various measures of inhomogeneity, Mw/Mn, U, etc., were examined. The function, σn/Mw, where σn is the standard deviation of the number distribution, is considered as a measure of the relative distribution. It is shown to be almost constant throughout the degradation.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110302
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  • 9
    Electronic Resource
    Electronic Resource
    Effects of interfaces on the thermal degradation of polymer-metal compositesProd. No. 1458 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 357-368 
    Details
    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: Previous studies by Black and Blomquist on the degradative failure of polymer-metal adhesive bonds have shown that composite failure depends largely on the type of metal substrate employed. In the work reported herein, metal powders of high surface area have been employed to maximize the metal-polymer interface. The composite systems studied consisted for aluminum and iron with polycondensates of bisphenol A-diglycidyl ether, phenol-formaldehyde and poly-2,2′-(m-phenylene)-5,5′-bibenimidazole. The composites were prepared in the absence of air and thermally degraded in a time-of-flight mass spectrometer while the degradation products were continuously monitored from mass 1 to 200. In the polymer and polymer-metal systems investigated, iron accelerated the decomposition of all polymers studied. This was determined by plotting m/e against degradation temperature for the more common mass peaks such as hydrogen and carbon monoxide for the carbon-hydrogen-oxygen-containing polymer and hydrogen cyanide and ammonia for the carbon-hydrogen-nitrogen-containing polymer. This technique offers promise in determining the nature of the interface as well as the effect of the interface on polymer degradation.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110304
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  • 10
    Electronic Resource
    Electronic Resource
    Graft copolymers of starch. III. Copolymerization of gelatinized wheat starch with acrylonitrile. Influence of chain modifiers on copolymer compositionProd. No. 1476 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 457-463 
    Details
    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 study was made of the influence of selected chain modifiers on both the molecular weight of grafted polyacrylonitrile and the grafting frequency of the starch-polyacrylo-nitrile graft copolymer. Gelatinized wheat starch was used with ceric ammonium nitrate as the initiator. The organic chain modifiers investigated were ethyl mercaptan, 1-dodecanethiol, methyl ethyl ketone, acetaldehyde, and chloroform. Sodium chromate, cupric bromide, cupric nitrate, cupric acetate, and cupric chloride were also tested as chain modifiers. In the presence of cupric chloride, there was a tenfold reduction in the molecular weight of grafted polyacrylonitrile; however, fewer chains were grafted to the starch backbone than were observed without cupric chloride.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110312
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