Considering the numerical values obtained for
the first two constants
1
K
and
2
K
, reported in Table
(the other constants are almost zero, indicating that
no reversion is experienced) at two distinct
temperatures, it appears interesting to plot the
straight lines passing from such values in the
Arrhenius plane. In such space, the horizontal axis is
represented by the inverse of the absolute
temperature,
T/1
, whereas the vertical axis is
i
Klog
, where
i
K
is the i-th kinetic constant. It is,
indeed, commonly accepted that the variability of a
single kinetic constant follows the so called
Arrhenius law, which may be written as
TR
E
ii
g
ai
eKTK
0
, where
0i
K
is the value of the i-th
kinetic constant at an infinite temperature,
ai
E
is a
constant typical of the reaction and
g
R
is the
universal gas constant. In a
T/1
-
i
Klog
Cartesian
plane, the Arrhenius law is thus represented by a
straight line, intercepting vertical axis at
0
log
i
K
.
Since experimental data are available at two distinct
temperatures, and accepting that each single constant
follows an Arrhenius law, it is possible to sketch
TK
i
lines in the
T/1
-
i
Klog
plane, for both
peroxides under consideration. Such representation
is particularly useful from a practical point of view,
because it allows a direct evaluation of the kinetic
constants describing the velocity of the partial
reactions at any vulcanization temperature. The
straight lines numerically deduced are depicted
inFigure 13. Subfigures refer to peroxides M2 (-a),
BC-FF (-b) and 14-S (-c) respectively. Numerical
data of Table 1, utilized to plot the straight lines, are
also indicated for the sake of clearness. In order to
evaluate if the numerical approach proposed is in
agreement with simplified procedures commonly
used in practice, it is also possible to compare
numerical results with commercial data available for
both peroxides under consideration. In particular,
Akzo Nobel furnishes in tabular form values of the
kinetic constants of both BC-FF and 14-S at three
different temperatures, corresponding to a half-time
life equal to 0.1, 1 and 10 hours respectively. It is
implicitly assumed that the reaction describing
peroxide decomposition is of first order and that the
single kinetic constant associated to such a reaction
follows and Arrhenius law. It is very straightforward
the deduction of the numerical values of the
constants at the three temperatures considered, from
the experimental knowledge of the half time life
2/1
t
, being simply
2/1
2ln tK
i
. No information is
available for M2, which is indeed a mixture of
peroxides.
Since in our numerical model, first and second
reactions occur in series, and the first reaction
produces 2
R
radicals, the comparison with the
simplified practical approach above discussed, may
be attempted considering the weighted average
between constants
1
K
and
2
K
, i.e. plotting the
straight line 1/3*(2 log
1
K
+log
2
K
), again deduced
from present numerical results and represented with
a dash-dot line in Figure 13-b and Figure13-c for
Perkadox BC-FF and Perkadox 14S-FL respectively.
In the same figures, data deduced from commercial
catalogues provided by Akzo Nobel (2012) are
represented with circles. As it is possible to notice,
the agreement is almost perfect, meaning that the
predictivity of the numerical procedure here
presented is very promising.
3 CONCLUSIONS
In the present Part II, the numerical model proposed
in Part I has been validated using the huge amount
of experimental data obtained by the authors, in
presence of three different curing agents with
different concentrations at three increasing
temperatures. The numerical model provides partial
reactions kinetic constants, which are very useful in
practice to determine the optimal industrial input
parameters to use (as for instance vulcanization
temperature and curing time) to obtain the maximum
mechanical properties of the vulcanized items. A
comparison with simplified approaches based on a
single first order kinetic equation shows that very
reasonable results are obtained and, at the same
time, demonstrates that the model proposed
supersedes the classic limitations of the simplistic
procedures commonly used, especially in presence
of reversion or when a mixture of peroxides is
utilized. An interesting correlation between tensile
strength and maximum torques has been also
obtained.
The traditional methods used by producers to
choose the most suitable production parameters, as
for instance a-priori strategies (essentially based on
the rheometer curves) or a-posteriori considerations
(direct tensile tests on the vulcanized rubber) could
be potentially avoided and superseded, after a
careful calibration of the mathematical approach
proposed, with an undoubted advantage in terms of
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Applications
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