
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