Abstract
AbstractSimultaneous interpenetrating polymer networks (SIN) based on diglycidyl ether of bisphenol‐A (DGEBA) and unsaturated polyester (UP) in weight ratios of 100/0, 50/50, and 0/100 were blended and cured simultaneously by using cumene hydroperoxide (CHP) and m‐xylenediamine (MXDA) as curing agents. A kinetic study during SIN formation was carried out at 43, 53, 58, and 64°C. Concentration changes for both epoxide and CC bond were monitored with Fourier transform infrared (FTIR). Rate expressions for epoxide polymerization were established with model reactions for phenyl glycidyl ether (PGE) and benzylamine in dichloroethane containing benzyl alcohol. Experimental results revealed that a lower cure rate constant for the CC bond during SIN formation was found, compared with pure UP network formation. A model of network interlock is proposed to account for this phenomenon. During simultaneous cure of DGEBA and UP, the network interlock should provide a sterically hindered environment, which subsequently retards cure rate for UP. On the other hand, epoxide cure during SIN formation indicates higher rate constants for both uncatalyzed and catalyzed reactions, compared with those of pure DGEBA cure. Presumably the catalytic effect of hydroxyl end groups in UP overcomes the effect of network interlock. Kinetic parameters were calculated and are discussed. © 1995 John Wiley & Sons, Inc.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
