Journal of Applied Polymer Science · 2006 · 47 citations · 20 references
Natural SciencesMaterials EngineeringMaterials ScienceMaterials ProcessingPolymer ChemistryPolymer EngineeringCatalytic Reaction KineticsChemical Reaction KineticsDegree Of ConversionKinetic ModelingPolymerization KineticsThermosetsAutocatalytic KineticsAutocatalytic ReactionsChemical-curing MechanismsCure TimeCuring KineticsReaction Order DeterminationReaction Rate PredictionResin Characterization
Abstract The cure kinetics of commercial phenol–formaldehyde (PF), used as oriented strandboard face and core resins, were studied using isothermal and dynamic differential scanning calorimetry (DSC). The cure of the face resin completely followed an n th‐order reaction mechanism. The reaction order was nearly 1 with activation energy of 79.29 kJ mol −1 . The core resin showed a more complicated cure mechanism, including both n th‐order and autocatalytic reactions. The n th‐order part, with reaction order of 2.38, began at lower temperatures, but the reaction rate of the autocatalytic part increased much faster with increase in curing temperature. The total reaction order for the autocatalytic part was about 5. Cure kinetic models, for both face and core resins, were developed. It is shown that the models fitted experimental data well, and that the isothermal DSC was much more reliable than the dynamic DSC in studying the cure kinetics. Furthermore, the relationships among cure reaction conversion (curing degree), cure temperature, and cure time were predicted for both resin systems. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1642–1650, 2006
20
Reaction Kinetics in Differential Thermal Analysis
H.E. Kissinger · Analytical Chemistry · 1957 · 13K citations
M. Virginia Alonso, Mercedes Oliet, Juan Manuel Pérez et al. · Thermochimica Acta · 2004 · 133 citations
Natural Sciences, Materials Engineering, Materials Science +14