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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 3499-3519 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic model has been developed and successfully applied to describe the reaction profiles of the seeded emulsion polymerization of styrene. The model incorporated a mechanism for the capture of aqueous-phase oligomeric free radicals by latex particles. Both the collision and diffusion mechanism were considered. The experimental data agreed well with the collision mechanism. The rate of the free radical capture by latex particles is proportional to latex particle surface area (D2p), and also is a strong function of the rate of free radical generation per latex particle. The model predicts that the rate of polymerization is dependent on the latex particle diameter to the 2.5 power in the gel region. This was demonstrated experimentally by J. W. Vanderhoff et al. (J. Polym. Sci., 20, 225 (1956)). Propagation and termination rate constants for styrene in the 70-90°C temperature range were also determined.
    Additional Material: 13 Ill.
    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 49 (1993), S. 1909-1919 
    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
    Notes: The mechanisms of fatigue crack initiation for various stress levels and thicknesses have been determined for single-edge notched specimens of polycarbonate and used to assemble a map. Three basic fatigue crack initiation mechanisms were identified and named as cooperative ductile (the damage zone formed ahead of crack consisting of yielded material), solo-crack brittle (very little damage zone development), and cooperative brittle (identified as a cloud of microcracks or crazes that developed at the notch tip). With a given applied stress and within the same failure mechanism, the values of the number of cycles to crack initiation decrease with increase in thickness. The transition from cooperative ductile to solo-crack brittle initiation mechanisms is sudden with increasing thickness. Transition from cooperative ductile to cooperative brittle with decreasing stress was less well defined. Regions where combinations of mechanisms were observed are also identified in the map. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 887-894 
    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 family of copolymers of ethylene and α-olefin resins with homogeneous branching distribution, which behaves as elastomers at high short-chain branching levels and acts as typical thermoplastics at low short-chain branching levels, is now available. Control of this broad range of properties stems from the ability to control the molecular architecture more effectively using Dow's INSITETrademark of The Dow Chemical Co. technology than in the past. Due to the unique combination of narrow short-chain branching distribution (SCBD) and narrow molecular weight distribution (MWD), these resins provide a unique opportunity to model structure/property relationships in branched ethylene-α-olefin copolymers. The modulus in branched ethylene-α-olefin copolymers with aliphatic branches is shown to be primarily dictated by crystallinity. It is shown that the branch distribution and the branch type have an insignificant effect on the modulus of ethylene copolymers containing aliphatic branches at a given crystallinity. Modulus data have been successfully modeled in such systems using a lamellar fiber-reinforced amorphous matrix composite model. Switching from aliphatic branches to cyclic branches significantly affected the modulus at similar crystallinities. © 1994 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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