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  • Chemistry  (7)
  • 1960-1964  (7)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 108-115 
    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: Polyester-urethane block copolymers were prepared by the block polyaddition reaction of diisocyanate with two kinds of linear polyesters, one of which was polyethylene terephthalate. The melting points of polyester-urethane block copolymers containing more than 30% polyethylene terephthalate are independent of the total molar fraction of the two polyester components, so that the melting point-composition curves are step-shaped. The relation between the second-order transition point of the block copolymer and its composition, on the other hand, is the same as that for a random copolymer. It is observed that some polyester-urethane block copolymers containing 15-50% of polyethylene terephthalate have elastic properties. For example, the 15/85 polyethylene terephthalate/polyethylene adipate-tetramethylene diisocyanate block copolymer has a tensile strength of 240 kg./cm.2 and an elongation of 700%. It may be supposed that these elastic properties are due to the structure of the block copolymer chains: the flexible polymer chains in the amorphous region may be joined to the crystallites of polyethylene terephthalate, so that a type of network structure similar to crosslinking is formed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    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: On assuming that the two polymer components are poorly compatible or incompatible and from semimicro heterogeneous systems composed of homogeneous phases of each component, two kinds of generalized models which relate the degree of mixing of the two phases to the mechanical behavior of the systems were proposed. In this phenomenological theory, the chemical interaction between the two polymer components was negelcted, and the stress or strain distribution along the boundaries between the two phases was much simplified. This might give serious error when the mixed phases become small and the surface effect, instead of volume effect, becomes significant. The mechanical mixtures can be classified by the manner of mixing of the two phases of A and B components as follows: A islands in B matrix, B islands in A matrix, A matrix-B matrix, and A islands-B islands mixing. The mechanical properties of the mixed systems are affected not only by those of each component and their volume fraction in bulk, but strongly by the manner of mixing. The terminology used here, as the degree of mixing, is one of the representations of the manner of mixing in terms of distribution function of partial volume fractions of each component in the mixed system.The analysis of some mixed systems of two polymer components gave the following results. The mixed systems cast from acetone solution of poly(vinyl acetate) and poly(methyl methacrylate) give mechanical mixtures of the islands-in-matrix type mixing. A phase conversion from PMMA islands in PVAc matrix to PVAc islands in PMMA matrix occurs at about 70% volume fraction of PMMA due to the hexagonal close packing of PMMA islands in PVAc matrix with increase of volume fraction of PMMA On the other hand, the systems cast from mixtures of acetone solution of PVAc and lightly crosslinked PMMA fine particles give mechanical mixtures of the matrix-matrix type mixing. The mixed systems of polystyrene and 30/70 butadiene-styrene copolymer, which have been classified by Tobolsky as polyblends, might also be a type of mechanical mixture classifiable as matrix-matrix mixing. However, the manner of mixing should be much modified by the chemical interaction between the two components.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 73 (1964), S. 225-230 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Kettenübertragungskonstanten substituierter Diphenyldisulfide bei der radikalischen Substanzpolymerisation von Methylmethacrylat wurden bestimmt. Der Substituenteneinfluß auf die Reaktivität der Disulfid-Bindung mit einem Polymethylmethacrylatradikal wurde bestimmt durch die Elektronendichte des Substituenten. Die Kettenübertragungskonstante gegenüber dem substituierten Diphenyldisulfid nahm mit zunehmendem negativem e-Wert des Monomeren zu.
    Notes: Chain transfer constants of substituted diphenyl disulfides in radical bulk polymerization of methyl methacrylate were determined. The effect of the substituent on the reactivity of the disulfide bond toward a polymethyl methacrylate radical was dependent on the electron density of the substituent. The chain transfer constant to substituted diphenyl disulfides increased negative e-value of the polymerizing monomer.
    Additional Material: 3 Ill.
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die NMR-Spektren einer Reihe von Modellverbindungen wurden untersucht zur Identifizierung der stickstoffhaltigen Bindungen, die in den Elastomeren des Polyurethantyps anzunehmen sind. Es ergab sich, daß Harnstoffe, Urethane, Allophanate und Biurete durch ihre verschiedene chemische Verschiebung unterschieden werden können, wenn die Messung in polaren Lösungsmitteln wie Dimethylacetamid, Dimethylsulfoxyd u.a. durchgeführt wird. Die Methode wurde ferner für die Analyse von linearen Prepolymerisaten aus Polypropylenglycol und Diphenylmethan-4,4′-diisocyanat oder Tolylendiisocyanat angewandt.
    Notes: The NMR spectra of a series of compounds were taken in order to identify the nitrogen-containing linkages which had been considered to be present in polyurethane elastomers. It has been found that the urea, the urethane, the allophanate and the biuret can be discriminated each other by their different chemical shifts when the measurement is made in polar solvent like N,N-dimethyl acetamide, dimethyl sulfoxide, etc. The method was further applied to the analysis of the uncured linear prepolymer prepared from polypropylene glycol and diphenylmethane-4,4′-diisocyanate or tolylene diisocyanate.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2135-2143 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyacrylonitrile heated under appropriate conditions (time and temperature) in nitrogen or in vacuo was found to be photosensitive. On exposure to visible light, the visible light absorption of a heat-treated polyacrylonitrile film shifts to longer wave length, and an ESR absorption is detected in heat-treated powder. Solubility to acids changes on exposure to light, and acids of appropriate concentration dissolve only the unexposed portion of a polyacrylonitrile film and leave the exposed portion. The relation between these effects of light on dry-heated polyacrylonitrile is discussed.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2965-2976 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: p-Bromostyrene, p-methylstyrene and α-methylstyrene were subjected to polymerization in liquid sulfur dioxide with α,α'-azobisisobutyronitrile as an initiator at polymerization temperatures of 0-60°C. In case of polymerization of p-bromostyrene, only polysulfones of 1:2 molar ratio between sulfur dioxide and p-bromostyrene were obtained. No cationic polymerization was observed. In case of polymerization of p-methylstyrene polysulfone having 1:2 composition, a radical polymerization product, as well as poly-p-methylstyrene, a cationic polymerization product, as obtained, revealing concurrent and competitive occurrence of both polymerizations. The cationic polymerization was explained as the result of the electron-donating property of the para-methyl substituent and the catalytic action of sulfur dioxide or sulfurous acid formed with a minute amount of water contained in liquid sulfur dioxide. In liquid sulfur dioxide, the cationic polymerization was perfectly inhibited by DMF and the radical polymerization was not affected by the presence of DMF. In a system in which the radical polymerization alone proceeded in liquid sulfur dioxide, the overall rate of the polymerization was proportional to the concentration of AIBN in the order of 0.7. This was interpreted to indicate that the strong solvation between sulfur dioxide and the terminal radical of the growing radical due to hyperconjugation of the p-methyl group may stabilize the terminal radical, leading to a unimolecular termination. In the polymerization of α-methylstyrene, the addition of AIBN did not give polysulfone, but gave poly-α-methylstyrene alone as a result of cationic polymerization.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 227-230 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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