Glass-Transition Temperature: Conversion Relationship in the Polycyclotrimerization of 4,4*-Thiodiphenylcyanate

Polycyclotrimerization of 4,49-thiodiphenylcyanate was adopted as a model system for general thermosetting polymers for studying the relationship between the glass-transition temperature (Tg) and conversion (a) during network formation. Exist- ing expressions for Tg-a relationship were used and compared. The experimental Tg-a data were well fitted to several one-parameter equations although the physical signif- icance of parametric values thus obtained could not be unambiguously identified. Among the two-parameter models, both the Hale-Macosko-Bair equation and the so-called "original" DiBenedetto equation were well fitted by experimental data (when the mean-field crosslink density was used), yielding parametric values consistent with the original designated physical meanings within the corresponding theoretical frames. Relationships between the parameters in different theories were also discussed. Inci- dentally, a discontinuity of DCpTg at the gel point was observed (i.e., DCpTg is of different values in the pregel and postgel regimes, respectively). © 2000 John Wiley &

[1]  Jin‐Long Hong,et al.  Effect of Intramolecular Cycles on the Polycyclotrimerization of Aromatic Dicyanates , 1999 .

[2]  Jin‐Long Hong,et al.  Effect of intramolecular cycles on the formation of rigid polycyanate networks , 1997 .

[3]  Jin‐Long Hong,et al.  Kinetics of polycyclotrimerization of 4,4′-thiodiphenylcyanate , 1995 .

[4]  Sindee L. Simon,et al.  Conversion–temperature–property diagram for a liquid dicyanate ester/high‐Tg polycyanurate thermosetting system , 1994 .

[5]  J. Galy,et al.  Isothermal curing of an uncatalyzed dicyanate ester monomer : kinetics and modeling , 1993 .

[6]  J. K. Gillham,et al.  Cure kinetics of a thermosetting liquid dicyanate ester monomer/high-Tg polycyanurate material , 1993 .

[7]  C. Macosko,et al.  Characterization and modeling of rigid branched polycyanates , 1993 .

[8]  M. Gottlieb,et al.  Effect of crosslinks on the glass transition temperature of end-linked elastomers , 1992 .

[9]  G. Martin,et al.  Analysis of the curing behavior of cyanate ester resin systems , 1991 .

[10]  C. Macosko,et al.  Glass Transition Temperature as a Function of Conversion in Thermosetting Polymers , 1991 .

[11]  H. Stutz,et al.  A generalized theory for the glass transition temperature of crosslinked and uncrosslinked polymers , 1990 .

[12]  Jean Pierre Pascault,et al.  Glass transition temperature versus conversion relationships for thermosetting polymers , 1990 .

[13]  A. Dibenedetto,et al.  Prediction of the glass transition temperature of polymers: A model based on the principle of corresponding states , 1987 .

[14]  P. Couchman Thermodynamics and the compositional variation of glass transition temperatures , 1987 .

[15]  C. Feger,et al.  Properties of partially cured networks. 2. The glass transition , 1985 .

[16]  J. K. Gillham,et al.  Time–temperature–transformation (TTT) cure diagram: Modeling the cure behavior of thermosets , 1983 .

[17]  Roberto J. J. Williams,et al.  The evolution of thermosetting polymers in a conversion–temperature phase diagram , 1982 .

[18]  F. E. Karasz,et al.  A Classical Thermodynamic Discussion of the Effect of Composition on Glass-Transition Temperatures , 1978 .

[19]  Douglas R. Miller,et al.  A New Derivation of Post Gel Properties of Network Polymers , 1976 .

[20]  C. Macosko,et al.  A new derivation of average molecular weights of nonlinear polymers. , 1976, Macromolecules.

[21]  M. J. Richardson,et al.  Derivation of Accurate Glass Transition Temperatures by Differential Scanning Calorimetry , 1975 .

[22]  E. Grigat,et al.  Chemie der Cyansäureester, I. Cyansäureester aus Hydroxylverbindungen und Halogencyan , 1964 .

[23]  Robert Simha,et al.  On a General Relation Involving the Glass Temperature and Coefficients of Expansion of Polymers , 1962 .