Radical induced cationic frontal polymerization (FP) is a technique that allows the curing of huge epoxy parts (e.g., rotors of generators, and construction composites) as well as parts with < mm within minutes instead of hours to days using only a fraction of the energy. Even harsh environmental conditions, like being submerged in water, cannot stop the FP
Dispersion of carbon nanotubes and carbon nanofibers is a crucial processing step in the production of polymer-based nanocomposites and poses a great challenge due to the tendency of nanofillers to agglomerate. One of the most effective methods for dispersion is the use of a three-roll mill, which is a well-established method and results in agglomerates below 5 µm. Nevertheless, this process is time-consuming and thus a limiting factor for industrial applications. Our aim was to establish an easy and efficient ultrasonic dispersion process, characterize the dispersion parameters, and compare both methods, ultrasonication and the three-roll mill. We applied rheological tests and analyzed the agglomerate sizes by an image fit of the microscopy images. All these analyses combined deliver a valuable set of information about the dispersion’s quality and, therefore, allows the improvement and further adaptation of the dispersion process.
In this study, a new type of prepreg technology has been established using a dual curing system consisting of 1,6-hexanediol diacrylate (HDDA) and frontally polymerisable components based on the epoxide resin. The study of the polymerisation of HDDA revealed (tert-butylcyclohexyl)peroxydicarbonate (BCPC) as the most suitable radical thermal initiator. The presence of BCPC resulted in a fast radical polymerisation of HDDA and no cationic ring-opening reaction of the epoxy, which was observed by monitoring the double bond and epoxy group conversion in real time-NIR rheology measurement. The formed prepreg can subsequently be cured by radical-induced cationic frontal polymerisation of the epoxy resin. Effects of HDDA amount on the radical polymerisation, stiffness of the gel, frontal parameters and thermal mechanical properties of final polymers were investigated. With 10 wt% HDDA, the formed prepreg has very good storage stability, which was proved by monitoring the epoxy group conversion during 4 months of storage at 50 °C while still a stable front can be obtained. Furthermore, the RICFP-prepregs with different fibre contents were prepared and polymerised by RICFP. Then, a snowflake composite was successfully produced using RICFP-prepreg. Graphic abstract