Graphene–polyamide-6 (PA6) composites with up to 17.0%·w/w graphene content were prepared via melt mixing. Oscillatory rheometry revealed that the dynamic viscoelastic properties of PA6 decreased with the addition of 0.1%·w/w graphene but increased when the graphene content was increased to 6.0%·w/w and higher. Further analysis indicated that the rheological percolation threshold was between 6.0 and 10.0%·w/w graphene. The Carreau–Yasuda model was used to describe the complex viscosity of the materials. Capillary rheometry was applied to assess the steady shear rheology of neat PA6 and the 17.0%·w/w graphene–PA6 composite. High material viscosity at low shear rates coupled with intense shear-thinning in the composite highlighted the importance of selecting the appropriate rheological characterisation methods, shear rates and rheological models when assessing the 3D printability of percolated graphene–polymer composites for material extrusion (ME). A method to predict the printability of an ME filament feedstock, based on fundamental equations describing material flow through the printer nozzle, in the form of a printing envelope, was developed and verified experimentally. It was found that designing filaments with steady shear viscosities of approximately 15% of the maximum printable viscosity for the desired printing conditions will be advantageous for easy ME processing.

The transition of additive manufacturing (AM) from a technique for rapid prototyping to one for manufacturing of near net or net components has been led by the development of methods that can repeatedly fabricate quality parts. High speed laser sintering and the recently developed multi-jet fusion (MJF) processes have seen quick adoption from industry due to their ability to produce high-quality components relatively fast. However, the recommended refresh ratios of new powder led to notable amounts of used powder being discarded. In this research, polyamide-11 powder, typically used in AM, was thermally aged to investigate its properties at extreme levels of reuse. The powder was exposed to 180 °C in air for up to 168 hours and its chemical, morphological, thermal, rheological, and mechanical properties were examined. To decouple the thermo-oxidative aging phenomena from AM process related effects, such as porosity, rheological and mechanical properties characterisation was performed on compression moulded specimens. It was found that exposure notably affected the properties of both the powder and the derived compression moulded specimens within the first 24 hours of exposure, but consecutive exposure did not have a significant effect.