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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 72 (1992), S. 3294-3304 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The problem of adhesion at the interface between two polymers is investigated using a fracture mechanics approach. The effect of viscoelastic deformation of the bulk polymers and the micromechanical behavior of the interface on the fracture toughness of the interface was investigated by analyzing the problem of a steadily growing interface crack under the condition of small scale yielding. This condition assumes that the region of displacement discontinuity across the interface (the adhesive zone) due to loss of adhesion is small compared with typical specimen dimensions. It is found that the amount of inelastic or viscous energy dissipation is strongly coupled to the interface behavior and that the measured interface fracture toughness can be much higher than the intrinsic interface fracture toughness. For sufficiently high crack growth rates, a simple expression is obtained which relates the rate of viscous energy dissipation and the intrinsic interface fracture toughness to the viscoelastic properties of the bulk polymer. The dependence of the stress field inside the adhesive zone and the length of the adhesive zone on the viscoelastic properties of the polymer, the applied loading, the interface micromechanical model and the crack growth rate a(overdot) is obtained by numerically solving an integral equation. The size of the region of the viscoelastic energy dissipation is found to scale with a(overdot)τr , where τr is the retardation time of the bulk polymer.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 72 (1992), S. 3305-3316 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: In the small scale yielding limit, the viscoelastic energy dissipation and the predicted fracture toughness of the interface between two viscoelastic polymers are monotonically increasing functions of the crack growth rate. For a finite size specimen however such prediction are no longer strictly valid. We demonstrate here that there is a maximum viscoelastic energy dissipation (and thus fracture toughness) at a characteristic interface crack velocity which depends not only on the micromechanical properties of the interface and the viscoelastic properties of the bulk polymers but also upon the specimen dimensions. Our analytical results allow us to deduce G=Gad[1+φ(aTa(overdot),c)] which relates the experimental fracture toughness to the intrinsic fracture toughness of the interface Gad, the WLF shift factor aT and c, a dimensionless parameter which is a function of the micromechanical properties of the interface, the mechanical properties of the polymers and the specimen dimensions. This result is similar to an empirical relation developed to fit experimental results; this relation however was assumed to be independent of c (specimen geometry). We demonstrate that the dependence of φ on c is substantially weaker than its dependence on aTa(overdot), which accounts for the success of the empirical relation in correlating the experimental data.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 52 (1988), S. 101-102 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The diffusion of deuterated polystyrene (d-PS) in a polystyrene matrix was used to probe the damage to the polymer surface caused by reactive ion beam etching (RIBE). Diffusion was seen to be hindered in a d-PS film treated by RIBE, an immobilization apparently due to crosslinking of the surface monolayer of the polymer sample.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 61 (1987), S. 5137-5149 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We consider front formation and steady-state front motion in a one-dimensional polymer system undergoing case-II diffusion. The polymer system approximates a polymer sheet whose thickness is very small compared with its lateral dimensions. The osmotic pressure of Thomas and Windle (TW) is used in the theoretical analysis. The transient problem of front formation is formulated. It is found that the original coupled system of partial differential equations proposed by TW can be reduced to one equation. An exact solution of this equation for a diffusion front moving with a velocity V is presented. The solution allows us to predict the dependence of the steady-state velocity on material parameters and the equilibrium concentration of penetrant outside the sheet. The concentration and pressure profile ahead of the moving front is obtained. We also show that the TW Model predicts the existence of a Fickian tail ahead of the steadily moving front. Conditions for the dominance of the Fickian tail are determined. The predicitions of our theoretical analysis are then compared with concentration profiles of iodohexane diffusing into polystyrene determined from Rutherford backscattering spectrometry.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 61 (1987), S. 5129-5136 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The swelling of a polymer glass by sorption of a small molecule penetrant is considered in a regime characterized by so-called case-II diffusion. Attention is focused on the polymer so that the swelling process can be investigated apart from diffusion. The model of Thomas and Windle (TW) is used to predict the surface swelling as a function of exposure time. This model assumes that the swelling is driven by the osmotic pressure which relaxes to zero as the surface penetrant volume fraction φs approaches its equilibrium value φe. The rate-controlling factor of the swelling process is the viscosity of the polymer η, which decreases with increasing surface sorption according to η=η0 exp(−mφ) where η0 is the viscosity of the unswollen polymer. For large values of M=mφe, φs is very small until a time τ is reached beyond which the swelling then accelerates rapidly towards its equilibrium value. This feature is absent if M〈e. The time τ is estimated by asymptotic analysis. Rutherford backscattering spectrometry is used to investigate the surface swelling kinetics of polystyrene by iodohexane. The TW model tends to underestimate the swelling rate when φs is low and to overestimate it when φs is high. Nevertheless, the time for φs to approach its equilibrium value φe is approximated well by the TW model.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 64 (1994), S. 2655-2657 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We propose a mechanism for creating lateral order in thin films of a homopolymer mixture via spinodal decomposition in the presence of a laterally structured substrate surface. The system under consideration is a mixture of deuterated polystyrene and partially brominated polystyrene (PBrxS, x=0.5) spuncast onto different substrates from toluene solution. We demonstrate that periodic stripe-like domain structures can be observed in the polymer films after spinodal decomposition on a periodic array of Cr lines on a H-terminated Si surface. The effect vanishes when the chemistry of the underlying structure is changed, strongly indicating an interface-driven ordering of the polymer film.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 10 (1994), S. 2466-2470 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 20 (1987), S. 1980-1985 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 21 (1988), S. 1513-1517 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 3075-3088 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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