on experimental data by means of the same GA
approach previously used with variable steam
temperature. Such lower and upper bounds values
for h are assumed in agreement with indications
provided in Milani et al. (2008).
We assume steam temperature constantly equal
to T
1
=202°C and the total curing time t
c
equal to 5.6
minutes, i.e. design conditions of Test #1 are
investigated, being the vulcanization level in such
case critical and unexpectedly low. Whilst authors
are aware that a realistic numerical simulation
should take into account the variability of both T
n
and h, such simulations cannot be performed with
the GA approach proposed if a relation between h
and T
n
is not provided.
However, it is worth underlining that the
evaluation of h (especially as a function of T
n
) is a
very difficult task, especially when steam condenses
and there is a passage between vapor and liquid
phase, due to unknown heat unsteady transfer
processes. In addition, the common Newton’s law of
heat exchange by convection is probably too
simplistic and holds only for forced convection,
whereas probably in this case –as already pointed
out- there is an unknown dependence of h with the
temperature difference between steam and rubber
surface.
It is finally worth emphasizing that the values
adopted for h in the two sets of simulations with
constant h represent large bounds indicated for
steam in forced convection in many handbooks and
therefore such numerical analyses may well
approximate upper and lower bonds.
Temperature profiles obtained assuming lower
and upper bound constant values for h are depicted
in Figure-a and –b respectively. Furthermore, in
Figure-c the same results are represented with a
variable h values. The numerical prediction of the
unreacted peroxide along the thickness of the cables,
with a comparison with experimentally determined
values is finally reported in Fig. 9.
As can be noted, when a large value for h is
assumed (upper bound) the heat exchange is
intuitively favored and the % unreacted peroxide
found numerically sensibly deviates from
experimental values.
The same applies for an excessively reduced
value of h (lower bound). In such a condition, the
heat exchange between rubber surface and steam
becomes slow and the peroxide reacts with lower
velocity. The resultant % of unreacted peroxide is
therefore higher than that experimentally
determined.
-a
-b
-c
Figure 7: Test #3. –a: temperature profiles at variable
temperature. -b: comparison with experimental data on
unreacted peroxide %. –c GA temperature profile.
Conversely, result obtained assuming h as
variable are in quite good agreement with
experimental evidences, see Fig. 9-c. h profile along
the tube length determined by means of the GA
proposed is represented in Figure 10, with a 3D
representation of the unreacted peroxide % (along
the thickness and length of the cable). As can be
noted, there is a monotonic decrease of h, which
assumes very high values at the beginning
(superheating condition) and then decreases along
the line to typical values for steam water convection.
While the present simulations are obviously affected
by errors induced by the strong simplifications
assumed, the results obtained give interesting
information on the physical processes occurring to
the steam along the line.
It is finally interesting to notice that, when
dealing with the initial inlet temperature, GA
simulations are performed assuming a value equal to
25°C.
0 20 40 60 80 100 120
0
20
40
60
80
100
120
140
160
180
200
tube length [m]
Temperature [°C]
internal layer
middle layer
external layer
0 0.5 1 1.5 2 2.5 3 3.5 4 4.5
0
0.5
1
1.5
2
2.5
3
3.5
distance from the external surface [mm]
% unreacted peroxide %
Experimental
Numerical
0 10 20 30 40 50 60 70 80
175
180
185
190
195
200
205
tube length [m]
water steam temperature [°C]
Experimental/FEMOptimizationofMediumVoltageRubberInsulatedElectricCablesVulcanizedwithSteamWater-
NumericalSimulationsandInverseAnalyses
33