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  • Chemical Engineering  (5)
  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 21 (1981), S. 970-977 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Craze healing was observed in many amorphous glassy polymers. A detailed study of the kinetics of craze healing in atactic polystyrene (Mw = 255,000) was conducted. The crazes were created in 0.08 mm films in air at room temperature, To, and constant stress, σo ⋍ 2,300 psi, healed at temperature Th for a time, Th, at σ = 0, and recrazed at To and σo. Nucleation times, τ1 and τ2, and growth rates, L1, and L2, for the first and second loading, respectively, were measured as a function of th and Th for individual crazes using dark field optical microscopy. Complete optical and mechanical healing was observed for Th ≥ 70°C(Tg ≅ 100°C). At constant Th, healing progressed in five stages with increasing th as follows; (i) no healing, τ2 = 0, L2 ≫ L1; (ii) partial healing, τ2 〈τ1, L2 〉 L1; (iii) similar growth, τ2 = τ1, L2 = L1; (iv) slower growth, τ2 〉 τ1, L2 〈 L1; (v) disappearance, τ2 → ∞, L2 → 0. A craze healing envelope of Th vs Th was obtained for the above stages. Craze healing occurred by line mode in which uniform healing occurred along the entire length of the craze.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 52-57 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 lap shear joint method was used to study strength development during welding of polystyrene surfaces- The surfaces previously had not been in contact and care was taken to insure rapid wetting of the interface. The shear stress at failure, τf was measured at room temperature as a function of contact time, t, at constant welding temperatures up no 20°C above the glass transition temperature, Tg. The time dependence of welding could be well described by τfαt1/4. This result is in agreement with predictions of the reptation molecular dynamics model applied to inter-diffusion at a symmetric amorphous polymer-polymer interface. The activation energy for the thermally activated increase in strength development was determined as E = 96 kcal/mol at T = 113.5°C, which compares with E = 93,2 kcal/mole as predicted by the W-L-F theory using C1 = 13.7, C2 = 50 and Tg = 100°C. The polystyrene samples had molecular weights, Mn = 143,000 and Mw = 262.000. The time to achieve complete healing, t∞ ≍ 256 min at 118°C, was found to be of the same order of magnitude as the viscoelastic relaxation time and also with the time required for a polymer chain to diffuse a distance equal to its root mean square end-to-end vector.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 805-815 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Infrared (IR) spectroscopy was used to study molecular deformation processes in polymers as a function of stress, strain, time and temperature. Stress-induced frequency shifts were found to depend on temperature and morphology. Deformation of viscoelastic polypropylene was examined in terms of time dependent molecular stress distributions, orientation changes, conformational variations, and chain fracture. A tie chain length distribution model was used to quantitatively interpret the IR data. Molecular deformation processes of creep and stress relaxation were found to be opposite in nature, Observed long lifetimes of highly stressed chains suggest a reappraisal of existing fracture theories.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 1340-1367 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Studies of strength development at polymer-polymer interfaces are examined and applications to welding of similar and dissimilar polymers are considered. The fracture properties of the weld, namely, fracture stress, σ, fracture energy, GIc, fatigue crack propagation rate da/dN, and microscopic aspects of the deformation process are determined using compact tension, wedge cleavage, and double cantilever beam healing experiments. The mechanical properties are related to the structure of the interface via microscopic deformation mechanisms involving disentanglement and bond rupture. The time dependent structure of the welding interface is determined in terms of the molecular dynamics of the polymer chains, the chemical compatibility, and the fractal nature of diffuse interfaces. Several experimental methods are used to probe the weld structure and compare with theoretical scaling laws, Results are given for symmetric amorphous welds, incompatible and compatible asymmetric amorphous welds, incompatible semicrystalline and polymer-metal welds. The relevance of interface healing studies to thermal, friction, solvent and ultrasonic welds is discussed.
    Additional Material: 33 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 24 (1984), S. 1130-1137 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 of valence-coordinate deformation to the temperature dependence of some infrared peak-absorption frequencies in Poly(vinyl chloride) (PVC) and polystyrene (PS) is stated. A skeletal band and a CH2 rocking band in PVC and a ring-mode band in PS were studied in two kinds of experiments: steady heating and cooling of a quenched (nonequilibrium, glassy) sample through its glass-transition temperature, Tg, and long-term annealing of quenched samples below Tg, followed by steady heating and cooling. The results, a slope discontinuity, ΔM, in the v(T) relation at Tg and a frequency shift, Δviso, during isothermal annealing below Tg, are analyzed in two theoretical approaches. Interchain and intrachain contributions to the observed frequency shifts are expected to occur with a differing relative significance in different kinds of molecular vibrations, leading to one possible method of distinguishing valence-coordinate deformation (chain strain) from other effects.
    Additional Material: 8 Ill.
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