1. |
Statistical distribution analysis of rubber fatigue data |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5887-5891
J. L. DeRudder,
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摘要:
Averagerubber fatigue resistance has previously been related to such factors as elastomer type, cure system, cure temperature, and stress history. This paper extends this treatment to a full statistical analysis of rubber fatigue data. Analyses of laboratory fatigue data are used to predict service life. Particular emphasis is given to the prediction of early tire splice failures, and to adaptations of statistical fatigue analysis for the particular service conditions of the rubber industry.
ISSN:0021-8979
DOI:10.1063/1.329825
出版商:AIP
年代:1981
数据来源: AIP
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2. |
Use of a theoretical equation of state to interpret time‐dependent free volume in polymer glasses |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5892-5897
J. G. Curro,
R. R. Lagasse,
R. Simha,
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摘要:
Many physical properties of polymer glasses change spontaneously during isothermal aging by a process commonly modeled as collapse of free volume. The model has not been verified rigorously because free volume cannot be unambiguously measured. In the present investigation we tentatively identify the free‐volume fraction with the fraction of empty sites in the equation of state of Simha and Somcynsky. With this theory, volume recovery measurements can be analyzed to yield directly the time‐dependent, free‐volume fraction. Using this approach, recent volume measurements on poly(methyl methacrylate) are analyzed. The resulting free‐volume fractions are then used in the Doolittle equation to predict the shift in stress relaxation curves at 23 °C. These predicted shift factors agree with the experimental measurements of Cizmeciogluetal. In addition, it is shown that previous assumptions concerning temperature dependence of free volume are inconsistent with the theory.
ISSN:0021-8979
DOI:10.1063/1.329826
出版商:AIP
年代:1981
数据来源: AIP
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3. |
Sub‐subTgstructural relaxation in glassy polymers |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5898-5902
H. S. Chen,
T. T. Wang,
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摘要:
Structural relaxation in a temperature range from 32 to 62° K glass transition has been investigated, for the first time, for a nearly monodisperse polystyrene using a differential scanning calorimeter and a thermal mechanical analyzer. Low temperature anneals in the vicinity of 320 K stabilize the glassy structure and lead to volume contraction. Upon heating, the annealed samples show an excess endothermic peak and exhibit a gradual expansion associated with structural recovery above the annealing temperature. Significantly, the samples recover the initial heat content and volume without reheating through the glass transition temperature. This sub‐Tgstructural relaxation behavior is in many respects distinct from that commonly observed near the glass transition. Kinetics of relaxation processes are also discussed.
ISSN:0021-8979
DOI:10.1063/1.329827
出版商:AIP
年代:1981
数据来源: AIP
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4. |
Longitudinal polarization of &agr;‐poly(vinylidene fluoride) by kink propagation |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5903-5905
J. D. Clark,
P. L. Taylor,
A. J. Hopfinger,
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摘要:
The &agr;‐ phase chain of poly(vinylidene fluoride) has a component of dipole moment parallel to the chain axis which can be reversed by propagation of a solitary wave along the chain. Calculations of the energy required to create such a wave in a perfect chain yield larger values than are implied by experiment. This suggests that either head‐to‐tail defects or regions of stress at the lamellar boundary might play an important role in causing the observed dielectric behavior.
ISSN:0021-8979
DOI:10.1063/1.329828
出版商:AIP
年代:1981
数据来源: AIP
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5. |
Temperature dependence of broadline NMR spectra of water‐soaked, epoxy‐graphite composites |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5906-5907
David Lawing,
R. E. Fornes,
R. D. Gilbert,
J. D. Memory,
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摘要:
Water‐soaked, epoxy resin‐graphite fiber composites show a waterline in their broadline proton NMR spectrum which indicates a state of intermediate mobility between the solid and free water liquid states. The line is still present at −42 °C, but shows a reversible decrease in amplitude with decreasing temperature. The line is isotropic upon rotation of the fiber axis with respect to the external magnetic field.
ISSN:0021-8979
DOI:10.1063/1.329829
出版商:AIP
年代:1981
数据来源: AIP
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6. |
The annealing of solution grown crystals of alpha and gamma poly(vinylidene fluoride) |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5908-5915
D. T. Grubb,
K. W. Choi,
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摘要:
Single crystals of poly(vinylidene fluoride) PVF2have been grown from dilute solution and sedimented to form oriented mats. The product was &agr;‐PVF2or a mixture of &agr;‐ and &ggr;‐PVF2and different morphologies were observed for the two phases. Annealed mats exhibited complex melting behavior, due in part to melting and recrystallization. Plots of melting temperature against reciprocal lamellar spacing indicate equilibrium melting points of 443.5 and 457.3 K for rapidly crystallized &agr;‐ and &ggr;‐PVF2after 1‐h anneal, and fold surface free energies of 15.6 and 27.2 mJm−2for &agr;‐PVF2from different solvents, 24.8 mJm−2for &ggr;‐PVF2. Long annealing times or high annealing temperatures tend to increase the melting point without changing the lamellar thickness probably due to rejection of head‐to‐head defects.
ISSN:0021-8979
DOI:10.1063/1.329830
出版商:AIP
年代:1981
数据来源: AIP
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7. |
Depolarization‐current study of low‐density polyethylene containing an antioxidant |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5916-5920
D. Ronarc’h,
S. Haridoss,
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摘要:
Thermally stimulated depolarization currents in low‐density polyethylene containing Irganox 1076 are investigated. The thermal sampling technique has been used to study the elementary processes constituting &bgr; and &ggr; relaxations. Irganox 1076 is found to increase the intensity of &bgr; and &ggr; peaks and not to change the activation parameters. The participation of the antioxidant in the molecular relaxation processes is discussed.
ISSN:0021-8979
DOI:10.1063/1.329831
出版商:AIP
年代:1981
数据来源: AIP
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8. |
Sub‐Tgannealing studies of advanced epoxy‐matrix graphite‐ fiber‐ reinforced composites |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5921-5925
Eric S. W. Kong,
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摘要:
Selected mechanical properties of symmetrically (±45°) reinforced 16‐lamina graphite/epoxy composites have been found to be affected by sub‐Tgannealing. Postcured specimens of Thornel 300 graphite/Narmco 5208 epoxy were sub‐Tgannealed at 140 °C for ca. 10, 102, 103, 104, and 105min, with a prior quenching from aboveTg. The ultimate tensile strength strain‐to‐break, and static toughness of the composite materials were found to decrease as a function of sub‐Tgannealing time. No weight loss was observed during the sub‐Tgannealing. The time‐dependent change in properties can be explained on the basis of physical aging which is related to free volume decrease in the non‐equilibrium glassy state of network epoxies. The results imply possible changes in composite properties with service time.
ISSN:0021-8979
DOI:10.1063/1.329832
出版商:AIP
年代:1981
数据来源: AIP
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9. |
Stretching induced &ggr;→&bgr; transition in poly (vinylidene fluoride) |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5926-5929
B. Servet,
D. Broussoux,
F. Micheron,
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摘要:
Transition from unoriented &ggr; to oriented &bgr; phases is followed during stretching poly(vinylidene fluoride) at 150 °C, using both x‐ray and small angle light scattering techniques. It is observed that the &ggr;→&bgr; transition occurs simultaneously with the morphologic transition from spherulitic to fibrillar state. The threshold draw ratio is &lgr;?2, corresponding to a chain orientation functionfH?0.5; the conversion into &bgr; phase is complete at draw ratios &lgr;?4.
ISSN:0021-8979
DOI:10.1063/1.328520
出版商:AIP
年代:1981
数据来源: AIP
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10. |
Integral equation method for calculating entropy of confined chains |
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Journal of Applied Physics,
Volume 52,
Issue 10,
1981,
Page 5930-5933
R. G. Priest,
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摘要:
An important aspect of the thermodynamic properties of chain molecules in solids is the amount of entropy that is associated with rotations about bonds. Of particular interest is the high‐pressure hexagonal phase of polyethylene. This system is modeled for the purpose of this calculation as an assembly of chains confined to small cylinders. This paper describes an integral equation approach to the problem that may be viewed as a continuum limit of the transfer matrix technique. Two cases are solved: (1) the freely jointed chain confined to a cylinder small enough to prevent the chain from folding back on itself, and (2) the fixed bond angle chain confined to the same type of cylinder. The result of calculation (2) is discussed in light of a model for the high‐pressure hexagonal phase of polyethylene.
ISSN:0021-8979
DOI:10.1063/1.328521
出版商:AIP
年代:1981
数据来源: AIP
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