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Ulli Stier

Publications and source records attributed to Ulli Stier.

2 recordsLinked to original sources

Influence of the reaction mechanism on the time course of the entropy production during reversible polymerization.

The paper shows the influence of the reaction mechanism on the time course of the entropy production sigma in a closed system during reversible polymerization. We consider two different reaction mechanisms with (a) being a polycondensation and (b) a chain growth mechanism. For both mechanisms explicit expressions for the entropy production sigma as a function of time t are derived. To demonstrate the application of these general expressions we consider two different polymerization experiments where the reaction starts (i) from monomer molecules polymerizing to a defined number average chain length x(n,eq) and (ii) from monodisperse polymer molecules reacting with each other under the constraint that x(n) is the same at the beginning and the end of the reaction. In both cases we treat the system to be ideal and describe the kinetics of the reversible polymerization reactions using two kinetic constants for the forward and backward reactions, respectively. Under these assumptions the difference in the curvature of the entropy production sigma between a polycondensation and a chain growth mechanism is only marginal if the reaction starts from monomer molecules polymerizing to a defined number average chain length x(n,eq).

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Entropy production during reversible polymerization in nonideal systems.

A general route is shown to calculate the entropy production sigma as function of time t in a closed system during reversible polymerization. We treat the polymer molecules to behave nonideal and apply exemplarily the classical Flory-Huggins theory to get explicit expressions for the activity coefficient. At the beginning of the polymerization the system is in a nonequilibrium state where chemical reactions take place that irreversibly drive the system towards equilibrium with sigma approaching zero in the limit t-->infinity. The time-dependent course of the entropy production is explicitly calculated for two cases where the reaction starts (i) from monomer molecules polymerizing to a defined number average chain length xn,eq and (ii) from monodisperse polymer molecules reacting with each other under the constrain that xn is the same at the beginning and the end of the reaction. In both cases we find that the nature of the activity coefficient has an important effect on the curvature of sigma which may considerably differ from that of an ideal behavior.

Journal Article↗