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Abbreviations
- A:
-
Area, B/kT
- B:
-
Activation energy at zero stress
- C:
-
Proportionality constant
- Di :
-
Scale factor for velocity; i=1, interface convolution; i=2, repeated cavitation
- E:
-
Young's modulus in general. With subscripts C, M, PB, PS, P: moduli of composite, matrix phase, polybutadiene, polystyrene, and particle, respectively
- ΔG:
-
Activation energy
- H:
-
Height of channel in which interface convolutes; craze tip opening displacement
- K:
-
Bulk modulus in general. With subscript C, M, PB, PS, P: bulk moduli of composite, matrix phase, polybutadiene, polystyrene, and particle, respectively
- KI :
-
Mode one stress intensity factor
- KIC :
-
Critical stress intensity factor for propagation
- N:
-
Surface density of crazable sites
- Q:
-
Functional dependence of negative pressure on deviatric stress for cavity expansion
- R:
-
Radius of particulate heterogeneity
- T:
-
Absolute temperature
- V:
-
Volume
- W:
-
Toughness, total work to fracture
- Y:
-
Yield stress in general. With subscript cr, craze-yield stress
- Y(λn):
-
Tensile yield stress of polymer after uniaxial extension to an extension ratio of λn
- Ŷ:
-
Athermal tensile yield stress of a glassy polymer
- a:
-
Craze half length
- b:
-
Craze half thickness at craze center
- c:
-
Volume fraction
- f:
-
f(x)=u(x)+k(x), final half thickness of craze cavity under the craze traction σc
- g:
-
g(x), unconstrained half thickness of craze lentil after undergoing expansion
- k:
-
k(x), primordial half thickness of craze cavity
- n:
-
Total number of crazes, strain rate exponent in non-linear viscosity
- n0 :
-
Total number of internal particulate heterogeneities
- q:
-
Stress concentration factor
- s:
-
Deviatoric (shear) stress
- t:
-
Time in general. With subscripts f, in, inact: fracture, initiation, inactivation time
- u:
-
(=uy) u(x), displacement of half craze cavity under craze traction σc
- v:
-
Velocity of craze
- w:
-
Width of sample in general. With subscripts l, s in the long and short direction
- x:
-
Coordinate
- y:
-
Coordinate
- z:
-
Coordinate
- Δ:
-
Mean distance between surface crazes
- Δ:
-
Length of cavitational process zone
- χ:
-
Surface free energy, surface tension
- β:
-
Aspect ratio of a craze, =a/b
- γ:
-
Volumetric coefficient of expansion in general. With subscripts C, M. PB, PS, P: composite, matrix, polybutadiene, polystyrene, particle, respectively
- δ:
-
Mean distance between crazes in the volume
- δ:
-
With subscripts, A, B: solubility parameter
- δ:
-
With subscripts, A, B, solubility parameter
- ε:
-
Uniaxial strain in general. With subscripts f, m, z: fracture, maximum at cavitation, and in the extension direction, respectively
- λ:
-
Wave length of convoluted interface
- λn :
-
Extension ratio
- λ′n :
-
As defined in Eqn. (51)
- ν:
-
Poisson's ratio of polystyrene. With subscripts C, M, P: composite, matrix, particle, respectively
- ϱ:
-
Active craze front length per unit volume. With subscripts C, M, P: composite, matrix, particle, respectively
- σ:
-
Negative pressure specifically. With subscripts c, e, i, m, P, ST, TH, ∞: craze traction, Mises equivalent, one of three principal stresses, maximum level of craze traction where cavitation in PB begins, negative pressure in particle, negative pressure due to one of three principal stresses, negative pressure due to thermal mismatch, uniaxial applied stress at the borders
- σ:
-
With subscripts xx, yy, zz etc. for components of the local stress tensor
- θ:
-
Ratio of slope of the falling to the rising part of the traction cavitation law
- Θ:
-
Craze dilatation
- τ:
-
Time constant
- ξ:
-
Symbolic parameter describing defects. With subscripts e, i: extrinsic, intrinsic, respectively
- η0 :
-
Non-linear viscosity coefficient
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Argon, A.S., Cohen, R.E., Gebizlioglu, O.S., Schwier, C.E. (1983). Crazing in block copolymers and blends. In: Kausch, H.H. (eds) Crazing in Polymers. Advances in Polymer Science, vol 52-53. Springer, Berlin, Heidelberg. https://doi.org/10.1007/BFb0024060
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