• Wubbenhorst, Michael
• Mangialetto, Jessica
• Van Den Brande, Niko
• Mele, Bruno Van

Abstract

The molecular dynamics of the reversible network 4F230-2M230 were studied systematically by dielectric relaxation spectroscopy (DRS) at frequencies between 10–1 and 107 Hz under both isothermal and non-isothermal conditions, focusing on the cooperative segmental dynamics as sensed by the dielectric α-relaxation. This reversible network is based on the furan–maleimide Diels–Alder reaction of a 4-functional furan-functionalized Jeffamine coupled with a 2-functional maleimide. Different strategies for extracting a “dielectric” glass transition temperature (Tg) were employed and compared. First, relaxation times τα were derived by conventional Havriliak–Negami fits of dielectric spectra and then fitted to the Vogel–Fulcher–Tammann (VFT) equation, which yields the dynamic Tg of partially cured samples (approach I). Alternatively, the thermal glass transition temperature was derived from the dielectric spectra ε′(f, T) using a fine structure analysis by bivariate differential sampling. Both the dynamic and thermal Tgs revealed an excellent agreement, confirming the stability of the VFT fits as well as the equivalence of both quantities as usually expected for bulk glass-forming materials. Two attempts were made to find a unique set of VFT parameters based on a global fit considering DRS spectra from partially cured samples during heating from −120 to 100 °C. Via a first procedure (approach II), a unique set of VFT parameters EV and τ∞ was obtained that well describes the relaxation times during non-isothermal cure at temperatures where the effects of ongoing cure kinetics can be neglected. To overcome this restriction, a refined approach III was developed that includes the earlier reported kinetic model for the DA reaction and allows accurate predictions for the relaxation time evolution during both isothermal and non-isothermal cure experiments. Based on this unique description, a new technique for continuous cure monitoring was proposed and tested. This technique allows us to compute in real-time dynamic Tg from the relaxation time τα at any stage of the isothermal or non-isothermal cure process using two unique VFT parameters from the global fit procedure. This approach might stimulate new applications of DRS-based cure monitoring.

Topics

• impedance spectroscopy
• experiment
• glass
• glass
• molecular dynamics
• thermogravimetry
• glass transition temperature
• forming