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applying much lower external stress than for the process including simulta-
neous breakage of all atomic bonds by the sliding plane [3].
FIGURE 4.3 The relationship between theoretical t o and experimental t Y shear stresses
at yielding for polytetrafluoroethylene (1), HDPE (2), polypropelene (3), polyamide-6 (4),
poly(vinil chloride) (5), polyhydroxiester (6), PC (7), polysulfone (8) and PAr (9) [20].
Payerls and Nabarro [3] were the first who calculated the shear stress
necessary for the dislocations motion, t dm . They used a sinusoidal approxi-
mation and deduced the expression for t dm as follows:
2
1
G
-
2
p
ab
(1
-
n
)
t
=
e
i
i
,
(4.5)
dm
-
n
where n is the Poisson's ratio and parameters a i and b i are of the same mean-
ing as in Fig. 4.2 .
By substituting reasonable n value, for example, 0.35 [27], and assuming
a i = b i , the following value for t dm is obtained: t dm = 2 × 10 -4 G . Though for
metals this value is higher than the observed it Y , it is much closer to them
than the stress calculated using simple shear model (the Frenkel model , Fig.
4.1 ).
However, for polymers the situation is opposite: analogous calculation
indicates that their t dm does not exceed 0.2 MPa, which is by two orders of
magnitude, approximately, lower than the observed t Y values.
 
 
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