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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 2811-2816 
    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 concept of gross melt fracture of polymer melts as a tensile failure in the die entry region was supported in this work by the observation of a dramatic increase in the melt fracture of poly-ethylene extrudates upon lubricating thoroughly a conical, converging extrusion die. This flow, according to an analysis using a Fromm viscoelastic model, was found capable of producing axial tensile stresses in the extrudate in excess of 106 dynes/cm2 at the very moderate exit shear rate (no lubricant) of 100 sec-1. A calculated stress level of about 5 × 106 dynes/cm2 caused sharp, deep transverse cuts to appear in the extrudate. The ability of tensile stresses of this magnitude to fracture melts was demonstrated by separate experiments run in simple tension on molten rods, using similar rates and total deformations. A large qualitative difference between high and low-density polyethylene in both these experiments was noted.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 15 (1976), S. 2313-2315 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 3
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The characterization of recently synthesized (Pro-Pro-Gly)n, n = 7, 8 is described, along with melting profile studies of its association equilibrium, and thermal quenching studies of the kinetics of its association reaction. The order of the kinetic reaction is about 3, implying that three peptide chains are involved in the activated state of the rate-limiting step. The reaction rate was found to exhibit a negative temperature coefficient. With the (Pro-Pro-Gly)7 peptide, the concentration dependence of the (Pro-Pro-Gly)n association equilibrium was observed for the first time.Detailed thermodynamic analysis for these n = 7, 8 data, together with literature data for n = 10, 15, 20 were carried out for both the simple “all-or-none” binding model and for a series of complex equilibrium models. For the latter, all of the (Pro-Pro-Gly)n data (in 10% acetic acid) are fit best with a maximally cooperative near-neighbor model with a standard enthalpy change ΔH = -650 cal/mole of residues, and a standard entropy change ΔS = -14.63 -10/n cal/deg-mole of residues, wherein the -10 eu represents an end-effect contribution to the binding free energy.With regard to optical rotatory properties and thermodynamic parameters, the data for the new n = 7, 8 peptides match rather well with the literature data for the n = 10, 15, and 20 peptides.The enthalpic stabilization per residue of the triple-helical form of (Pro-Pro-Gly)n was nearly an order of magnitude smaller than the enthalpic stabilization per additional proline obtained from direct calorimetric measurements on native collagens of different (and much lower) proline contents by Privalov and Tiktopulo. [Biopolymers (1970) 9, 127-139.] Possible explanations for this phenomenon are discussed.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 1375-1389 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three isomeric nonconjugated dienes, o-, m- and p-(2-vinyloxyethoxy)styrenes, were selectively polymerized by anionic or radical initiators through the styryl double bond while leaving the vinyl ether moiety intact. The anionic-initiated polymeric products are of high molecular weight and narrow molecular weight distribution as characterized by membrane osmometry and gel-permeation chromatography, respectively. These polymers were subsequently crosslinked by cationic initiators via the vinyl ether moiety on the polymer side chains. Acid-catalyzed hydrolysis of the poly(2-vinyloxyethoxy)styrenes yielded their respective hydroxy-containing polymers, polyvinylphenoxyethanols. The latter were physically and spectroscopically identical to authentic samples prepared by radical polymerization of the corresponding vinylphenoxyethanols, which, in turn, were synthesized by hydrolysis of the (2-vinyloxyethoxy)styrenes. The polyvinylphenoxyethanols were shown to undergo many chemical transformations, such as esterification with 3,5-dinitrobenzoyl chloride, cyanoethylation, and urethane formation.
    Additional Material: 7 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 15 (1977), S. 277-282 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3315-3328 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymeric methacrylates functionalized with free methacryloyl groups are efficiently crosslinked in the presence of transition-metal carbonyls on UV irradiation of the polymeric solid. The reaction proceeds by a radical chain mechanism with a kinetic chain length of about 10 in a solvent-free polymer containing 10-3 mole of methacryloyl groups per cm3. The chain length increases steeply when the glass transition of the polymer is reached, either by plastification or by an increase in temperature. The temperature dependence of the crosslinking yield below the glass transition is consistent with an activation energy of about 9 kcal mole-1. The addition of acrylic monomers enhances chain propagation by up to an order of magnitude. Postirradiative crosslinking in the matrix comes to a standstill well before all acrylic groups or radicals have been exhausted: if, after cessation of the primary reaction, the matrix is briefly heated, a second crop of crosslinks is obtained without further exposure. The system behaves thus as if the radicals had been removed into traps from which they can be set free by thermal activation. From an analysis of the reaction kinetics it appears that in the glassy polymer 90% of the radicals are inactivated in this way. Radical recombination, however, is the principal mechanism of chain termination above the glass transition. From the kinetic data, diffusion coefficients for polymer-bound groups are found to be in the range of 10-17-10-16 cm2 sec-1 in the glassy polymer at room temperature. They are of the order of 10-14 cm2 sec-1 in plasticized films above the glass transition.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 14 (1976), S. 375-380 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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