For semicrystalline thermoplastics, the temperature-time behavior during cooling of the melt can significantly affect the formation of crystalline structures (e.g., spherulite sizes, the degree of crystallization, crystal modifications, etc.) and hence, the resulting global component properties. In this paper, the crystallization of polyamide 12 at different cooling rates as well as process-based temperature-time profiles during cooling were investigated analytically with fast scanning calorimetry. Furthermore, based on analytical results, foils were extruded at different cooling conditions and tested mechanically and tribologically. The analysis reveals differences of the crystal melting behavior for different cooling conditions which is likely to originate in two different polymorphs of polyamide 12, c, and c 0 . Furthermore, mechanical investigations carried out with the extruded foils show that parts produced at high supercooling have less stiffness than parts produced at low supercooling, probably due to differences in the crystalline structures. Regarding tribological parameters, no clear differences could be measured. POLYM. ENG. SCI., 57:450-457, FIG. 5. Heat flow measured during cooling (left) and second heating (right) of PA 12 with respect to the examined cooling rates of 50-100 K/s. FIG. 6. Heat flow measured during cooling (left) and second heating (right) of PA 12 with respect to the examined cooling rates of 5-50 K/s.
Thermoplastic Polyurethane (TPU) is a unique tailorable material due to the interactions of hard and soft segments within the block-copolymer chain. Therefore, various products can be created out of this material. A general trend towards a circular economy with regards to sustainability in combination with TPU being comparably expensive is of high interest to recycle production as well as post-consumer wastes. A systematic study investigating the property changes of TPU is provided, focusing on two major aspects. The first aspect focuses on characterizing the change of basic raw material properties through recycling. Gel permeation chromatography (GPC) and processing load during extrusion indicate a decrease in molar mass and consequently viscosity with an increasing number of recycling cycles. This leads to a change in morphology at lower molar mass, characterized by differential scanning calorimetry (DSC) and visualized by atomic force microscope (AFM). The change in molar mass and morphology with increasing number of recycling cycles has an impact on the material performance under tensile stress. The second aspect describes processing of the recycled TPU to nonwoven fabrics utilizing melt blowing, which are evaluated with respect to relevant mechanical properties and related to molecular characteristics. The molar mass turns out to be the governing factor regarding mechanical performance and processing conditions for melt blown products.
A completely opposite injection molding filling behavior of thermosets and thermoplastics by an effective and useful method developed by the authors was found. Specifically, for the thermoset injection molding, there is a strong slip between the thermoset melt and wall surface, which is not found for the injection molding of thermoplastic materials. In addition, the variables, such as the filler content, the mold temperature, the injection speed, and the surface roughness that could lead to or influence the slip phenomenon of thermoset injection molding compounds, were also investigated. Furthermore, microscopy was conducted to verify the correlation between the mold wall slip and fiber orientation. The results obtained in this paper open challenges in the field of the calculation, analysis, and simulation of mold filling behavior of highly glass fiber-reinforced thermoset resins in the injection molding process with consideration of wall slip boundary conditions.
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