Data di Pubblicazione:
2002
Abstract:
The equilibrium heat capacity C-p of a liquid whose molecules polymerized
to form a linear chain structure at a fixed temperature has been measured
at a fixed frequency of 3.33 mHz in real time simultaneously with the
extent of polymerization alpha. The polymerization temperatures and this
frequency were chosen such that the fully polymerized state remained a
liquid and no heat capacity relaxation occurred. The plots of C-p against
alpha show a maximum. This confirms the recent theoretical conclusions
based on the polymer chain statistics [J. Wang and G. P. Johari, J. Chem.
Phys. 116, 2310 (2002)] that during the course of a melt's polymerization,
the configurational heat capacity of the equilibrium liquid reaches a
maximum value at a certain alpha, and then decreases to the finite value
of the fully polymerized melt. The results are also discussed in terms of
the potential energy landscape at a fixed temperature where each new
covalent bond formed and/or a new molecular weight distribution causes the
state of the sample to enter a new landscape with a new set of potential
energy minima of different depths and widths.
Tipologia CRIS:
01.01 Articolo in rivista
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