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  • Polymer and Materials Science  (59)
  • crystallization  (1)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 405-406 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    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 8 (1964), S. 455-466 
    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 relationship between the cut growth and fatigue failure of natural rubber vulcanizates under repeated loading is examined. The cut growth behavior has been investigated using several types of test piece, and the results are shown to be consistent when interpreted in terms of the tearing energy concept developed previously. The most comprehensive data have been obtained by measuring the growth of a small cut in the edge of a strip cycled in simple extension. It is found that the cut growth per cycle is approximately proportional to the square of the maximum tearing energy attained during the cycle. Using this relation, the fatigue life of a specimen containing a small cut is deduced from elasticity theory as a function of initial cut size and maximum strain. Experimental results give good agreement with theory. A similar strain dependence is found for the fatigue life of die-stamped dumbbell test pieces with no intentionally produced flaws; this is consistent with the mechanism of failure being cut growth from small flaws present in the specimens. Their effective size is estimated to be about 2 × 10-3 cm, which is compatible with the observed superficial imperfections of the cut edges.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4517-4522 
    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 sol content of previously extracted samples of lightly crosslinked silicone rubber has been found to increase during prolonged storage under relatively mild conditions. Simultaneously, the tensile stress slowly decreases in samples held stretched, and the equilibrium degree of swelling increases somewhat. Thus, the polymer network appears to undergo slow decomposition. This process is accelerated by moisture, by ammonia vapor, and by raising the temperature of storage. It is slowed down by prior treatment of the polymer with a silazane reagent which reduces the number of residual OH groups. It is therefore attributed to hydrolytic decomposition of the poly(dimethylsiloxane) molecules initiated by OH groups.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 943-960 
    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: Rates of wear have been determined for several elastomer materials, using a razor-blade abrading apparatus based on one described by Champ, Southern, and Thomas. Measurements have been carried out at different levels of frictional power input, corresponding to different severities of wear, at both ambient temperature and at 100°C, and both in air and in an inert atmosphere. It is concluded that wear occurs as a result of two processes: local mechanical rupture (tearing) and general decomposition of the molecular network to a low-molecular-weight material (smearing). Marked differences were shown by different elastomers. Carbon-black-filled natural rubber, SBR (styrene-butadiene copolymer) and EPR (ethylene-propylene copolymer) were particularly susceptible to decomposition and smearing, but for natural rubber and SBR the decomposition process was not observed in an inert atmosphere. It is attributed to molecular rupture under frictional forces followed by stabilization of the newly formed polymeric radicals by reaction with oxygen, if present, or with other polymer molecules, or with other macroradicals. Cis-polybutadiene and trans-polypentenamer did not appear to undergo smearing to a significant degree. The reactive radicals formed in these materials by molecular rupture are assumed to undergo rapid addition to other molecules so that the network structure is maintained. Rates of wear have been found to increase with the applied frictional force raised to a power n. The value of n was between 2.5 and 3.5 for unfilled materials at ambient temperature, in agreement with Champ, Southern, and Thomas, who pointed out a general correlation with mechanical fatigue. Filled materials were found to be less sensitive to the frictional force, whether wear took place by tearing or by smearing, having values of the index n of 1.5-1.8. Several observations suggest that wear, even in the absence of smearing, is not fully correlated with mechanical fatigue: the markedly lower wear rates for carbon-black-filled materials, the anomalous rankings of unfilled materials, and the relatively small effects of raising the test temperature to 100°C. It is concluded that abrasive wear by small-scale tearing is not accounted for solely by the crack growth properties of the material but involves other failure processes as well.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 4689-4700 
    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: An analysis is given of the force F required to pull an adhesive tape of unit width away from a rigid substrate in terms of the strength Ga of adhesion, the tensile modulus E of the tape, and its thickness t. Measurements are reported for several commercial adhesive tapes and compared with the predictions of the theory. Excellent agreement is obtained, suggesting that the theory is basically correct. Attention is drawn to the unusual form of the dependence of the failure force F upon the work Ga of detachment and the resistance Et of the tape to stretching in this case: F4 ∝ EtGa3. Even though the tape is assumed to be linearly elastic, the markedly nonlinear (cubic) relation between force F and displacement δ of the tape away from the substrate leads to this unusual result. Differences observed in Ga from pull-off and from 90° peeling experiments are tentatively attributed to additional energy losses in the latter case due to the severe bending deformations imposed on the tape as it is peeled away.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 5385-5398 
    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: An experimental study is described of the tensile modulus E of elasticity, tear strength Gc, and strength Ga of adhesion to a Mylar substrate, for PVC gels prepared with a wide range of PVC concentrations and with four different plasticizers. The modulus E, measured under quasiequilibrium conditions, was found to be approximately proportional to c3, where c is the volume concentration of PVC. The tensile behavior suggests that the molecular strands comprising the undiluted elastic network are relatively short, only about 26 C atoms long. Gc under threshold conditions was found to vary with c2.25 and to be considerably larger than (about 10 X) the value expected for a molecular network of short PVC chains. This difference is attributed to yielding of crystallites before molecular rupture can take place. Adhesion of PVC gels to Mylar was relatively weak. Both the tear strength and strength of adhesion were strongly dependent upon rate of fracture propagation and temperature, in good accord with the WLF rate-temperature equivalence for simple glass-forming substances. Thus, the strength of PVC gels appears to be determined largely by the glass temperature of the composition, and not by the amount or type of plasticizer except insofar as they affect the glass temperature.
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 5 (1967), S. 47-61 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyethylene networks were prepared by γ-irradiation of linear polyethylene, both molten and crystalline. The elastic and photoelastic properties of the networks were studied at high temperatures, i.e., in the molten state. The equilibrium swelling was also measured in several solvents. Values of the crosslinking efficiency G of γ-radiation, the molecular, weight Me between entanglements, the optical anisotropy α of the equivalent random link, and the polymer-solvent interaction parameter μ are deduced. Samples prepared by irradiation in the amorphous state showed markedly non-Gaussian elastic behavior. The presence of a large non-Gaussian term in the optical anisotropy is also deduced. The value of α obtained for swollen samples, which showed substantially Gaussian elastic behavior, was 3.9 × 10-24 cm.3, about one-half of that obtained for dry samples. It corresponds to an equivalent random link of only about 5 CH2 units, on the basis of Denbigh's values for bond polarizabilities. The samples prepared by irradiation in the crystalline state showed lower values for α, which also depended upon the degree of crosslinking. This is attributed to the nonrandom chain configurations prevailing at the time of crosslinking. The same samples were found to show more nearly Gaussian elastic behavior, which is attributed to the same cause.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1483-1487 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Expansion of a small spherical hole in a highly elastic solid is treated theoretically. Both elastic and surface energy terms are considered; the corresponding surface forces are assumed to be additive. The surface energy of the elastomer is assumed to be similar to that of simple liquids. Pressures or triaxial tensions required to inflate pre-existing holes to an indefinitely large size are calculated. Small holes require extremely large pressures, of the order of 1000 atm for holes of 10 Å radius. These results suggest a means of determining the distribution of hole sizes in elastomers and account in principle for experimental observations of cavitation processes. Detachment of the elastomer from a small rigid inclusion is treated in a similar way. The general absence of dilation or cavitation on stretching carbon black-filled elastomers is thus accounted for solely in terms of the small size of these filler particles.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 447-464 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements are described of the rates of crystallization and crystal melting temperatures in stretched test pieces of trans-polyisoprene, crosslinked to various degrees. The increase in rate with extension are attributed to the corresponding increases in melting temperature and hence degree of supercooling. The rise in the melting temperature of both the α- and β-crystal forms is found to be in satisfactory agreement with Flory's treatment of oriented crystallization. The changes in tensile stress are also generally in accord with the formation of oriented crystallites. For the more lightly crosslinked materials, a pronounced rise in tensile stress occurred during the later stages of crystallization, at extensions below about 100%. Reasons are given for attributing this phenomenon primarily to the relatively large contraction in volume on crystallization, rather than to the formation of folded-chain crystallites.
    Additional Material: 16 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 5 (1967), S. 157-164 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rates of growth of single ozone cracks have been measured for vulcanizates of two butyl rubbers over the temperature range of 20-160°C. Over most of this range the rates are quantitatively related to the segmental mobility of the polymer and depend upon temperature in accord with the appropriate from of the WLF relation. The rates are also proportional to the concentration of ozone. It is therefore concluded that diffusion of ozone into the polymer before reaction is the rate-controlling step. This is contrasted with the behavior of butadiene-styrene copolymers, for which the rates of crack growth are also quantitatively related to the segmental mobility, but the rates are somewhat larger at equivalent mobilities and the dependence upon ozone concentration is smaller. The difference is attributed to different penetration distances before reaction in polymers containing low and high densities of reactive sites.
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