Abstract
The upper liquid–liquid transition (Tlρ) was detected and investigated in unsaturated polyesters. This less known transition is caused by a stepwise decrease of intramolecular short-range local order that remains above the glass and lower liquid–liquid transitions. The local order is based on secondary valent interactions and is enhanced by hydrogen bonding, if possible, as in the polyesters under consideration. The Tlρ was detected as a change in the temperature dependence of the viscosity and electrical conductivity and differential scanning calorimetry thermograms revealed an endothermic change, above which the activation energy of crosslinking decreased. The Tlρ temperature was lower in a polyester containing a diole with more flexible structure. The changes in electrical conductivity and 1H NMR spectra indicated that the breaking of hydrogen bonding caused the Tlρ. Its intramolecular nature resulted in low sensitivity to crosslinking and addition of solvents. Near-IR spectroscopy was chosen for further investigation because of its greater sensitivity to structural changes in polymers than mid-IR. The spectra were recorded at selected temperatures. Significant intensity changes and wavelength shifts of hydroxyl and carbonyl absorptions at 1430 and between 1900 and 2100 nm, respectively, occurred at the Tlρ, while carbon–hydrogen absorptions showed only minor changes. This confirmed that breaking of the hydrogen bonding was responsible for disruption of the short-range local order. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 129–145, 2001
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Polymer Science Part B: Polymer Physics
Disclaimer: 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.