Biobased plastics have the potential to be sustainable, but to explore their circularity further, current end-of-life options need to be broadened. Mechanical recycling is one of the most accepted methods to bring back plastics into the loop. Polyhydroxybutyrates (PHBs) are biobased and biodegradable in nature with promising properties and varied applications in the market. This study focuses on their potential for mechanical recycling by multiple extrusion cycles (E1–E5) and multi-faceted characterization of the virgin (V) and reprocessed materials from E1 to E5. The behavior is compared to polypropylene (PP) as a reference with a similar property profile, which has also been reprocessed five times. The thermal properties of both series showed a stable melting point and thermal decomposition temperature from thermal analyses (differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA)). However, a steady increase in the degree of crystallinity was observed which could counterbalance the decrease in molecular weight due to repeated extrusion measured by gel permeation chromatography and resulted in similar values of tensile strength across the cycles. The strain at break was impacted after the first extrusion, but no significant change was observed thereafter; the same was observed for impact strength. Even in scanning electron microscopy (SEM) images, virgin and E5 samples appeared similar, showing the stability of morphological characteristics. Fourier transform infrared spectroscopy (FTIR) results revealed that no new groups are being formed even on repeated processing. The deviation between the PHB and PP series was more predominant in the melt mass flow rate (MFR) and rheology studies. There was a drastic drop in the MFR values in PHB from virgin to E5, whereas not much difference was observed for PP throughout the cycles. This observation was corroborated by frequency sweeps conducted with the parallel plate method. The viscosity dropped from virgin to E1 and E2, but from E3 to E5 it presented similar values. This was in contrast to PP, where all the samples from virgin to E5 had the same values of viscosity. This paper highlights the possibilities of mechanical recycling of PHB and explains why future work with the addition of virgin material and other additives is an area to be explored.

The thermal properties of the mold influence the cooling situation in the injection molding process. While there are experimental studies investigating the influence of special mold materials, they are limited to few polymers. In this work, an extensive parameter study with the simulation software Autodesk Moldflow Insight was performed to analyze the influence of the polymer itself on the impact of the mold steel on cycle time and warpage. The investigated part was a box with two thickness variations. A conventional mold steel was compared with a steel grade featuring approximately double the thermal conductivity. Simulations were performed with 18 polymers covering the most common material families. The main finding of this study was that the influence of the higher mold conductivity on cycle time ranged from an almost negligible reduction (3%) up to a strong effect (24%), depending mainly on the used polymers, but also on the part thickness. For the cycle time reduction, a correlation was found, with the melt, mold and ejection temperature being the dominant influencing factors of the polymers. With this correlation, it was possible to estimate the potential of cycle time reduction for other polymers. The simulations also showed a positive influence of the higher mold thermal conductivity on part warpage.

The aim of this study was the investigation of the use of modified talcum for supporting crosslinking and as novel nucleating agent for physical foaming of polyethylene. For the modification of the talcum, a thermal initiator was linked to the talcum surface. During the extrusion process, the initiator decomposes, and gas and radicals are formed. The gas generates the nucleation of cells and the radicals support the crosslinking process between the polymer chains. The modification of the talcum was performed in three steps: The first step was the grafting of alkoxysilanes onto the talcum surface. The second step was the chlorination of the thermal initiator for an easier linkage, and the last step was the linking between the initiator and the silanes grafted onto the talcum surface. For this study, two investigations were carried out. One investigation was the analysis of the crosslinking effect with the modified talcum. For this purpose, polyethylene plates were compression molded and the viscoelastic properties were measured with a parallel plate rheometer. The use of the modified talcum led to a higher crosslinking density. The second investigation was the physical foaming experiment in an extrusion process with nitrogen as blowing agent using both a pure and the modified talcum as nucleating agents. The foamed samples were characterized in terms of density, cell size and cell density, and compared with each other. The blend with the modified nucleating agent indicated a foam structure with a smaller mean cell size and a lower density compared to the use of the pristine nucleating agent.

Engineering polymers reinforced with renewable fibres (RF) are an attractive class of materials, due to their excellent mechanical performance and low environmental impact. However, the successful preparation of such composites has proven to be challenging due to the low thermal stability of RF. The aim of the present study was to investigate how different RF behaves under increased processing temperatures and correlate the thermal properties of the fibres to the mechanical properties of composites. For this purpose, hemp, flax and Lyocell fibres were compounded into polypropylene (PP) using a co-rotating twin screw extruder and test specimens were injection moulded at temperatures ranging from 180 °C to 260 °C, with 20 K steps. The decomposition behaviour of fibres was characterised using non-isothermal and isothermal simultaneous thermogravimetric analysis/differential scanning calorimetry (TGA/DSC). The prepared composites were investigated using optical microscopy (OM), colorimetry, tensile test, Charpy impact test, dynamic mechanical analysis (DMA) and melt flow rate (MFR). Composites exhibited a decrease in mechanical performance at processing temperatures above 200 °C, with a steep decrease observed at 240 °C. Lyocell fibres exhibited the best reinforcement effect, especially at elevated processing temperatures, followed by flax and hemp fibres. It was found that the retention of the fibre reinforcement effect at elevated temperatures can be well predicted using isothermal TGA measurements.

The long‐term stability of thermally conductive high‐density polyethylene (HDPE)‐based compounds as phase‐change material (PCM) is investigated. For this purpose, the HDPE's thermal conductivity (TC) is first enhanced via compounding two different filler types (expanded graphite and aluminum) into the polymeric matrix. Bulky specimens of these compounds are then stored in air for up to 7289 h in the melt state to investigate the compounds' long‐term stability as PCM. Their thermo‐oxidative/thermal stability and their ability to maintain the isotropic material character (homogeneous distribution of the incorporated particles) is investigated. The compounds' degradation behavior is monitored via Fourier‐transform infrared spectroscopy and the maintenance of the homogeneous filler distribution is examined via a combined differential scanning calorimetry/thermogravimetric analysis mapping of each exposed specimen. The storage capacity decreases minimally after 7289 h of exposure. Furthermore, the incorporated filler particles enhance the thermo‐oxidative stability of HDPE as PCM. Consequently, thermally conductive HDPE is a highly interesting PCM. © 2019 The Authors. Journal of Applied Polymer Science published by Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020, 137, 48269.