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1. |
Foreword |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 723-723
Abdelsamie Moet,
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ISSN:0032-3888
DOI:10.1002/pen.760241002
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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2. |
The role of molecular networks and thermally activated processes in the deformation behavior of polymers |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 724-736
I. M. Ward,
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摘要:
AbstractThe deformation behavior of three polymers, polyethylene terephthalate (PET), polymethylmethacrylate (PMMA), and linear polyethylene (LPE) is considered in terms of two key factors, the stretching of a molecular network and the influence of thermally activated processes. In PET the observation of a natural draw ratio leads to studies of shrinkage, shrinkage force, and optical birefringence to define the nature of the network. The network is further exemplified by measurements of the molecular reorientation in deformation bands, spectroscopic studies of molecular orientation in drawing, and the concept of a true stress‐strain curve. Yield and plastic deformation are also to be considered as thermally activated processes, but it appears that a major part of the flow stress is associated with the stretching of the molecular network. In PMMA the concept of a true stress strain curve also appears to be valuable, but the possibility of network breakdown during deformation has to be admitted as an extra complexity. In LPE the concept of a molecular network embracing both crystalline and non‐crystalline material is helpful in understanding the drawing behavior. There is also direct evidence for the existence of a network from measurements of shrinkage and shrinkage force, and the existence of a true‐stress strain curve. However, the dominant contribution to the flow stress now appears to come from thermally activated processes, with a key contribution from a small activation volume process which is tentatively associated with slip in the crystalline re
ISSN:0032-3888
DOI:10.1002/pen.760241003
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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3. |
A metallurgical approach to the pre‐yield and yield behavior of glassy polymers |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 737-749
B. Escaig,
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摘要:
AbstractThis paper discusses some new mechanical and small angle neutron scattering (SANS) data on glassy polymers, both thermoplastics and thermoset resins, from the point of view of dislocation‐like defects introduced in the molecular chain arrangement by deformation. In the pre‐yield stage, a new parameter, the work‐hardening rateKis introduced and its measurement is defined. Experiments are reported which show thatKcan be used as a very sensitive probe for microstructural changes during physical aging or curing. In one hand, the theory of yielding is revisited to make clear how dislocations and their propagation in polymers depend on specific features like entanglements and chain stiffness. On this basis, experimental internal stresses and activation volumes at yield (i.e., the temperature slope of yield stress) are accounted for. On the other hand, SANS data provide us with experimental evidence at the scale of 10 to 20 Å of the dislocation nature of the molecular “shear defects” introduced in the polymer by deformation. Finally, temperature is known to have a pronounced influence on yield processes. It is shown that two distinct deformation modes exist below and above a critical temperatureTc. AboveTc, a dislocation climb, which probably involves β‐processes, gives rise to a “diffusional” deformation mode where chains within a (diffuse) shear band are no longer oriented. A tentative formalization of this behavior, and its relation to the small strain creep of polymers, a
ISSN:0032-3888
DOI:10.1002/pen.760241004
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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4. |
Behavior and properties of shear bands |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 750-760
J. C. M. Li,
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摘要:
AbstractSome recent observations on shear bands in polymers are reviewed. These include intrinsic properties such as the mechanism of formation, the intersection of shear bands, the rate of propagation with and without obstacles, recovery of shear strain by annealing, and the stored energy in shear bands. Mechanical responses include the shear yielding criteria, reverse shear behavior and the Bauschinger effect, and the fracture of and at shear bands. Environmental effects include methanol transport in shear bands and in deformed poly(methvl methacrylate) in the region of mixed Fickian and case II behavior and methanol crazing of a shear banded material.
ISSN:0032-3888
DOI:10.1002/pen.760241005
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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5. |
Craze fibril formation and breakdown |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 761-769
Edward J. Kramer,
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摘要:
AbstractAs crazes grow in areal extent they also increase in width. The areal growth involves craze tip advance which has been shown to occur by the Taylor meniscus instability. Craze widening, at least for air crazes, occurs by drawing more fibrillar material from the craze‐bulk polymer interfaces at essentially constant extension ratio. Simple arguments will be given to predict the scale of the fibrillation in terms of the stress S at the craze tip and interfaces and an effective polymer surface energy (Γ) where:\documentclass{article}\pagestyle{empty}\begin{document}$$ {\Gamma = \gamma + {\raise0.5ex\hbox{$\scriptstyle 1$}\kern-0.1em/\kern-0.15em\lower0.25ex\hbox{$\scriptstyle 4$}}d \cdot v_E U_b} $$\end{document}which assumes that all entangled chain crossing the surface are broken [γ represents the van‐der‐Waals (intermolecular) surface energy,dis the entanglement mesh size,vEis the entanglement density, andUbis the energy required to break a single backbone bond]. These arguments also give the rate of fibrillation as a function of S, a nominal plastic resistance σyand Γ and can explain the fact that the stress for crazing increases relative to that for shear deformation as the entanglement density of the polymer is increased. The geometrically necessary entanglement loss (either by scission as assumed above or by disentanglement‐ at temperatures just belowTg) that accompanies fibril formation has important consequences for fibril stability. The probability p that a given entangled chain is lost can be computed from simple geometrical considerations knowing the fibril diameterD, its extension ratio λ and the mesh sized; p increases rapidly asDλ½becomes comparable to or less thand. These concepts can be tested in blends of high molecular weight polymer with chains of the same polymer that are too sho
ISSN:0032-3888
DOI:10.1002/pen.760241006
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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6. |
Microstructural aspects of failure in semicrystalline polymers |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 770-785
J. M. Schultz,
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摘要:
AbstractMicrostructural features of semicrystalline polymers are reviewed, as are the roles of chain properties and thermal history in their development. Experimental results relating failure properties to microstructural detail are described. General models to explain inter‐ and intra‐spherulitic failure behavior are proposed. Important are (a) the role of spherulite size in boundary incompatibility, (b) competition between spherulite boundary cracking and intraspherulitic yielding, (c) competition between localized (interspherulitic) fracture and dispersed (intraspherulitic) fract
ISSN:0032-3888
DOI:10.1002/pen.760241007
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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7. |
Deformation modes and fatigue behavior in styrene‐acrylonitrile and acrylonitrile‐butadiene‐styrene copolymers |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 786-797
J. A. Sauer,
C. C. Chen,
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摘要:
AbstractThe performance of styrene‐acrylonitrile copolymers under alternating stresses has been examined. Information has been obtained concerning the influence of acrylonitrile content and of molecular weight on thermal effects due to hysteresis, on cyclic lifetime to craze initiation, on average cycles to fracture, and on fatigue fracture surface morphology. The influence of an elastomeric second phase has been determined by comparing fatigue performance under comparable conditions of both styrene‐acrylonitrile (SAN) and acrylonitrile‐butadiene‐styrene (ABS). The stress concentrating effects of the rubber particles cause earlier initiation of fatigue‐induced damage and lower fatigue fracture resistance. The fatigue‐induced specimen temperature rise is greater in ABS than SAN and it increases linearly with test frequency and as the square of the stress amplitude. The fracture surface morphology of ABS, which differs from that of unmodified SAN and also from that of rubber modified polystyrene, i
ISSN:0032-3888
DOI:10.1002/pen.760241008
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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8. |
Kinetics of crack tip craze zone before and during fracture |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 798-808
W. Döll,
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摘要:
AbstractIrreversible deformations form the main energy consumption routes for absorbing supplied energy and thus determine the resistance of materials to fracture. In many polymeric materials under mode‐I loading conditions three regions of irreversible deformation behavior can be distinguished as a function of the stress intensity factorKIor strain energy release rateGI, respectively:no crack growth forKi
ISSN:0032-3888
DOI:10.1002/pen.760241009
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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9. |
Craze failure by midrib creep |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 809-813
Nicole Verheulpen‐Heymans,
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摘要:
AbstractIt has been known for some time that crazes thicken during growth mainly by drawing in fresh material from the craze‐bulk interface, keeping the average craze fibril draw ratio approximately constant. Since Creep effects contribute only negligibly to craze growth rates these effects have generally been considered unimportant regarding craze breakdown. However, it is also known that the first stage of fracture is failure of the craze midrib, which is a highly drawn, very thin region down the middle of a craze. Because of the very low thickness of the midrib it has little influence on craze behavior, and information on midrib behavior is difficult to obtain. It is the purpose of this paper to attempt to rationalize what information is availabl
ISSN:0032-3888
DOI:10.1002/pen.760241010
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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10. |
Stress and displacement fields at the tip of a craze containing a crack |
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Polymer Engineering&Science,
Volume 24,
Issue 10,
1984,
Page 814-819
William E. Warren,
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摘要:
AbstractPlane elasticity theory is utilized to obtain expressions for the stress and displacement fields at the tip of a craze containing a crack. The craze is modeled as a very thin elliptical inclusion with different elastic properties from hat of the surrounding bulk polymer. Problem is solved by superimposing the solution of a crack problem onto the solution for a uniformly loaded homogeneous craze. Invoking stress free boundary conditions on the crack surface provides a singular integral equation of Hilbert type with a unique solution. Contour lines of constant hydrostatic stress and constant maximum shear stress around the craze tip are shown graphically. These two stress combinations have played prominent roles in a number of proposed craze growth criteria. Results show that even for relatively long cracks within the craze, very little stress enhancement at the craze tip occurs. Only as the crack tip approaches the craze tip does the enhancement become significant, tending to drive the craze region ahead of the crack.
ISSN:0032-3888
DOI:10.1002/pen.760241011
出版商:Society of Plastics Engineers, Inc.
年代:1984
数据来源: WILEY
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