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  • Polymer and Materials Science  (39)
  • Aircraft Stability and Control  (2)
  • 1950-1954  (41)
  • 1945-1949
  • 1940-1944
  • 1953  (19)
  • 1952  (22)
Collection
Publisher
Years
  • 1950-1954  (41)
  • 1945-1949
  • 1940-1944
Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 321-335 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Vulcanization with sulfur is ascribed to the formation of sulfur radicals which are believed to copolymerize with the rubber molecule double bonds. Hydrogen sulfide is proposed as necessary for chain initiation but when formed in sufficient amounts serves as a chain terminator. This is believed to lead to numerous self-limiting features including ceiling temperatures, post-vulcanization and delayed action effects. Initiation may result from the oxidation of H2S to sulfur radicals and termination to the formation of HS radicals.
    Additional Material: 2 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 409-423 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When the acetate groups of polyvinyl acetate are removed and subsequently restored, the viscosity of the polymer is usually decreased. It is found that after such processing, vinyl acetate polymers prepared at a given temperature approach a maximum viscosity regardless of the viscosity of the original resins. This maximum is increased by lowering the temperature of polymerization and is different for other vinyl esters. The extent of degradation is negligible at low conversions. It is concluded that this phenomenon is characteristic of the monomer. The chemical bond responsible for the degradation has many of the properties of ester linkages. The resins degrade with both bases and acids although the latter catalyst sometimes requires the presence of water. They also degrade when heated in a solution of pyridine, acetic acid and acetic anhydride. The extent of degradation closely parallels the degree of hydrolysis. It is suggested that these ester linkages are formed during polymerization as a result of transfer with the carbon-hydrogen bonds of the acetate groups of both monomer and polymer. Evidence of another transfer reaction involving the vinyl group, but having no bearing on the degradation, is also advanced. If polyvinyl acetate is alcoholized with an acid catalyst, in the absence of water, the processed resin may have a higher viscosity than would be the case with an alkaline catalyst. How much higher is governed by the type of initiator used in the polymerization. This suggests that polymer molecules may be united under these conditions, but the nature of the reaction is obscure.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 4 (1953), S. 199-199 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 4 (1953), S. 150-151 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Branching and cross-linking are noted in emulsion and mass polymerizations involving vinyl benzoate and nuclearly substituted vinyl benzoates. A theory is proposed to account for this phenomenon based on free radical addition to the benzoate nucleus. Six new vinyl esters of substituted benzoic acids are described.
    Additional Material: 3 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 365-370 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reaction of polymethacrylamide, [-CH2C(CH3)(CONH2)-]n, in aqueous solution with hypobromite and hypochlorite has been investigated. Different reaction procedures yielded polymers which were similar, and which contained a small number of primary amino groups, considerable carboxyl and unreacted amide groups and, probably, alkylacylurea groups formed by interaction between adjacent isocyanate and halogenoamide groups. Analytical data supporting these conclusions are presented. The polymer from the Hofmann reaction is soluble in dilute alkali and also in strongly acid media, precipitating on dilution. Methacrylamide monomer reacts with hypochlorite to give N-α-methylvinyl-N′-methacrylurea and acetone.
    Additional Material: 5 Ill.
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  • 8
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When heated in a vaccum at 325° to 375°C., polystyrene yields mainly the monomer and some dimer, trimer, tetramer, etc., indicating that the breaks in the molecular chains occur largely at the ends. Polyethylene, under similar conditions, but at a some-what higher temperature, yields fragments of an average molecular weight of about 700, indicating that the molecular chains break, mostly at random positions. A study was made of rates of thermal degradation of these two polymers by measuring rates of loss of weight of samples by means of a very sensitive tungsten spring balance enclosed in a vaccum. The samples were limited to 5-6 mg. in order to avoid spattering during degradation. Rate curves plotted against per cent loss of weight by volatilization indicate that in the case of polystyrene the process is intermediate between a zero and first order reaction, while in the case of polyethylene, the process approximates a first order reaction. Activation energies were calculated on the basis of rates of degradation at various temperatures. The values thus obtained for polystyrene and polyethylene are 58 and 68 kilocalories, respectively.
    Additional Material: 14 Ill.
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  • 9
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Isobutylene and styrene were copolymerized at low temperatures, in methyl chloride solution, in the presence of aluminum chloride. The temperature was varied from -30 to -94°C., and the monomer/solvent ratio, the ratio of monomers, and the catalyst concentration were varied over a considerable range. The copolymerization equation was found to be applicable to the data, and the reactivity ratios were determined for various experimental conditions. For an “open” system in which the volume steadily increases during the course of polymerization, it is shown that the copolymerization equation is formally identical to that of Mayo and Lewis, except that concentrations are replaced by amounts of the reacting species. The temperature coefficients of the reactivity ratios in the present system are compared with those for free-radical systems; some important differences are noted. The reactivity ratios of isobutylene and styrene in the present system are greatly increased under conditions of turbulent agitation. A procedure for the compositional fractionation of the copolymers is described. The results are interpreted in terms of the copolymer chain structure; they appear to admit the postulate that the reactivity ratios and corresponding propagation rate constants are functions of chain length.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 11 (1953), S. 127-138 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymerization studies have been made on the three two-component systems formed by the monomers methyl acrylate, 2-vinylpyridine, and dichlorostyrene, and values of the monomer reactivity ratios were determined. Terpolymers were prepared from mixtures of these same monomers, and their compositions were compared with those predicted from the kinetic data for the copolymerizations. Measurements of dissymmetry of scattered light, molecular weight, and viscosity were made on solutions in acetic acid and in methyl ethyl ketone of a terpolymer containing 37 mole per cent methyl acrylate, 47 mole per cent 2-vinylpyridine, and 16 mole per cent dichlorostyrene. The molecular weight of the terpolymer is essentially the same in the two solvents but the polymer chain is more extended in acetic acid than in methyl ethyl ketone. In nitromethane solutions of the terpolymer the ηsp/c values increase sharply with decreasing concentration. This increase is eliminated if the solutions also contain 0.01 mole per liter of a substituted quaternary ammonium iodide. These facts indicate that the polymer behaves as a polyelectrolyte in nitromethane, presumably because of reaction between the aci-form of the solvent and the vinylpyridine groups.
    Additional Material: 7 Ill.
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