No abstract

The production of plastic has grown exponentially over the past few decades and with it the amount of plastic waste leaking in the environment, where it fragments into micro-and nanoplastics. This problematic situation stresses the need for increased plastic collection, recycling and reuse rates. Extrusion-based additive manufacturing (AM) and especially fused filament fabrication (FFF) offer an efficient and effective method to reuse and upcycle recycled plastic. This study focuses on poly(ethylene terephthalate) (PET), which has a broad application window and its recycling is therefore environmentally and economically favorable and sustainable. Therefore, this study involves the thermal and mechanical behavior of recycled PET after extrusion and 3D printing. The extrusion parameters are optimized by performing a complete physico-chemical and thermal analysis of the obtained filaments and they were compared with commercial virgin and recycled PET. Moreover, the influence of the applied processing conditions on the degree of crystallinity and mechanical properties is investigated. The filaments are then used for FFF, where various printing parameters are altered to obtain the optimum printing conditions (i.e. printing temperature, the build plate temperature, fan cooling and printing directions). The effect of the degree of crystallinity of semi-crystalline PET is investigated via altered printing parameters, showing superior mechanical properties for an increasing degree of crystallinity. To verify the portability of the obtained optimized print parameters, two different FFF printers are used. The use of recycled PET as feedstock for FFF supports the efforts for improving the sustainability of plastics by valorizing PET waste, and prolonging the lifecycle of PET.

No abstract

Epoxy-anhydride vitrimers are covalent adaptable networks, which undergo associative bond exchange reactions at elevated temperature. Their service temperature is influenced by the glass transition temperature (Tg) as well as the topology freezing transition temperature (Tv), at which the covalent bond exchange reactions become significantly fast. The present work highlights the design of high-Tg epoxy-anhydride vitrimers that comprise an efficient stress relaxation at elevated temperature. Networks are prepared by thermally curing aminoglycidyl monomers with glutaric anhydride in different stoichiometric ratios. The tertiary amine groups present in the structure of the aminoglycidyl derivatives not only accelerate the curing reaction but also catalyse the transesterification reaction above Tv, as shown in stress relaxation measurements. The topology rearrangements render the networks recyclable, which is demonstrated by reprocessing a grinded powder of the cured materials in a hot press. The epoxy-anhydride vitrimers are characterised by a high Tg (up to 140 °C) and an adequate storage modulus at 25 °C (~2.5 GPa), which makes them interesting candidates for structural applications operating at high service temperature.

Abstract:The viscosity of feedstock materials is directly related to its processability during injection molding; therefore, being able to predict the viscosity of feedstock materials based on the individual properties of their components can greatly facilitate the formulation of these materials to tailor properties to improve their processability. Many empirical and semi-empirical models are available in the literature that can be used to predict the viscosity of polymeric blends and concentrated suspensions as a function of their formulation; these models can partly be used also for metal injection molding binders and feedstock materials. Among all available models, we made a narrow selection and used only simple models that do not require knowledge of molecular weight or density and have parameters with physical background. In this paper, we investigated the applicability of several of these models for two types of feedstock materials each one with different binder composition and powder loading. For each material, an optimal model was found, but each model was different; therefore, there is not a universal model that fits both materials investigated, which puts under question the underlying physical meaning of these models.

To achieve future recycling targets and CO2 and waste reduction, the transfer of plastic contained in mixed waste from thermal recovery to mechanical recycling is a promising option. This requires extensive knowledge of the necessary processing depth of mixed wastes to enrich plastics and their processability in polymer processing machines. Also, the selection of a suitable processing method and product application area requires appropriate material behaviour. This paper investigates these aspects for a commercial processed, mixed waste, and two different mixed polyolefin fractions. The wastes are processed at different depths (e.g., washed/not washed, sorted into polyethylene, polypropylene, polyethylene terephthalate, polystyrene/unsorted) and then either homogenised in the extruder in advance or processed heterogeneously in the compression moulding process into plates. The produced recyclates in plate form are then subjected to mechanical, thermal, and rheological characterisation. Most investigated materials could be processed with simple compression moulding. The results show that an upstream washing process improves the achievable material properties, but homogenisation does not necessarily lead to an improvement. It was also found that a higher treatment depth (recovery of plastic types) is not necessary. The investigations show that plastic waste recovery with simple treatment from mixed, contaminated wastes into at least downcycling products is possible.

No abstract

No abstract