
Other
Select search scope: search across all journals or within the current journal

In this study, numerical approach for simulation of mold filling is presented. Polyurethane foam formation includes several complex phenomena such as chemical reactions, heat generation and blowing agent evaporation. Foam properties are variable during formation, foam viscosity increases and conductivity reduces. Foam phase is considered compressible and two phases are immiscible. Foam front will be captured by volume of fluid and appropriate governing equations will be implemented in OpenFOAM. This study prepares a numerical model to reduce several experimental runs with expensive prototypes for mold design.
Thermally insulating extruded polystyrene foams are currently produced with hydrofluorocarbon blowing agents. Hydrofluorocarbons have zero ozone depletion potential but rather high greenhouse warming potential. Various unsaturated fluoropropenes, with greenhouse warming potential values <15, have been assessed as HFC-134a replacements for styrenic extrusion foaming. The screening is first based on the modeling of solubility and diffusivity properties, followed by foaming experiments with a conventional extrusion process. Some fluoropropenes appear to be excellent blowing agents for extruded polystyrene foams and can be used alone for making very low-density foams with regular and large cell sizes, while some others require the use of a co-blowing agent for processing good quality foam. A few others are not suitable as a blowing agent for extruded polystyrene foams due to their toxicity or their very poor transport properties.
Thermoplastic polyurethane is a commonly used polymer in our daily lives. Microcellular injection molding (a.k.a. MuCell) is an emerging method capable of mass-producing thermoplastic polyurethane foams with tunable microstructures and properties. This study investigated the effects of four main processing parameters—namely, plasticizing temperature, carbon dioxide (CO2) content, injection volume, and injection speed—on microcellular injection molded thermoplastic polyurethane ASTM tensile test bars. Property variables of interest included the cell diameter, cell density, skin layer thickness, and Young’s modulus. Influence sequences of parameters on each variable were obtained via the orthogonal array test method. It was found that the CO2 content primarily affected the cell diameter and cell density, whereas the temperature mainly influenced the skin layer thickness and Young’s modulus. Surface fitting of each dependent variable was done by combining its two most influential parameters from the experiment data. The value of each property variable within the processing window could then be predicted from the fitted surface. In addition, microcellular injection molding of thermoplastic polyurethane was simulated by a commercial software package, and the simulated results confirmed the reliability of the cell diameter prediction.
This work is aimed at investigating the crystallization behavior of solid and microcellular injection molded polypropylene/nano-calcium carbonate composites. The effects of processing conditions, such as injection speed, mold temperature, and carbon dioxide concentration (used in microcellular injection molding), as well as the filler concentration on the crystal form, crystal orientation, and crystallinity were studied using 2D-wide-angle X-ray diffraction and differential scanning calorimetry. β-form crystals found in the surface layer of injection molded samples under high injection and mold temperature due to stronger shear effect. The orientation degree calculated from the X-ray diffraction images by the Hermans function was high in the surface layer and decreased as the distance from the mold surface increased. The addition of the nano-calcium carbonate filler promoted the formation of β-form crystals but reduced the orientation degree and crystallinity as the nanoparticles disturbed the orientation of the molecular chains. On the other hand, when using the foaming process, the formation of β-form crystals was inhibited and the orientation degree was reduced, but the crystallinity of the samples increased, likely due to enhanced molecular chain mobility from the supercritical carbon dioxide which acted as a plasticizer. The crystallinity of the samples was greater in the surface layer but showed no dependence on the injection speed or mold temperature.