Biomedical Engineering Reference
In-Depth Information
the case of mode II cracking in Fig. 23.2 . The difficulty here lies in the fact that the
most critical area of the crack, namely the crack tip has a jump in chemical potential
that cannot be captured using continuous functions, and further away from the crack
tip a discontinuous description fails as the chemical potential becomes increasingly
continuous.
High gradients are either approximated by
μ f ( x ,t) over the crack surfaces. In this case the decomposition
case 1: a jump
becomes
μ f ( x )
μ f ( x ,t)
μ f ( x ,t),
+ H Γ d ( x )
˜
(23.21)
[ μ f
and the difference in chemical potential at the discontinuity is given by
]
:
μ f ( x ,t) =
μ f ( x ,t), x
h
˜
Γ d .
(23.22)
The gradient in the chemical potential becomes
+ Γ d μ f n + ,
s μ f
s
μ f
s
μ f
=∇
+ H Γ d
(23.23)
or
case 2: a continuous enrichment of the chemical potential. In this case the decom-
position becomes
μ f ( x ,t). (23.24)
The distance function is defined with respect to the coordinates of the crack x Γ ,
namely by
μ f ( x )
μ f ( x ,t)
+ D Γ d ( x )
˜
2 ( x
n + , x
h
D Γ d =
x Γ )
·
Ω,
(23.25)
with h the magnitude of the Heaviside jump. The gradient
D
of the distance
function is given by
h
2 n +
Ω +
x
s
Ω = H Γ d n + ,
D =∇
D Γ d =
(23.26)
h
2 n
x
s u
u ) T
/ 2 holds.
The Heaviside function results in a discontinuous distribution with a jump at the
location of the crack and a linear distribution away from the crack (Fig. 23.3 a). The
distance function continuous distribution of the chemical potential with a nonlinear
distribution of the chemical potential away from the crack (Fig. 23.3 b).
where
=[∇
u
+
(
]
23.2.3 Local Behavior at the Crack
A local coordinate system ( n , s ) is introduced where n is in the direction of the
normal vector to Ω + and t is orthogonal in the direction of propagation. This means
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