RESUMO
In the injection molding process, weld line regions occur when a molten polymer flow front is first separated and then rejoined. The position, length, and angle of weld lines are dependent on the gate location, injection speed, injection pressure, mold temperature, and, especially, the direction and degree of the polymer melt velocity in the mold-filling process. However, the wall surface velocity of the thermoset melt in the mold-filling process is not zero, which is not found for thermoplastic injection molding. The main reason leading to this difference is the slip phenomenon in the filling phase between the thermoset melt and the wall surface, which is directly affected by the filler content. In this study, commercial thermoset phenolic injection molding compounds with different amounts of filler were employed to investigate not only the mechanism of weld line formation and development behind an obstacle in the injection molding process but also the flow disturbance of the thermoset melt in the spiral flow part. In addition, the effect of the wall slip phenomenon on the flow disturbance characterization and the mechanism of weld lines of selected thermoset materials was carefully considered in this research. Furthermore, the generated material data sheet with the optimal developed reactive viscosity and curing kinetics model was imported into a commercial injection molding tool to predict the weld line formation as well as the mold-filling behavior of selected thermoset injection molding compounds, such as the flow length, cavity pressure profile, temperature distribution, and viscosity variation. The results obtained in this paper provide important academic knowledge about the flow disturbance behavior as well as its influence on the mechanism of weld line formation in the process of thermoset injection molding. Furthermore, the simulated results were compared with the experimental results, which helps provide an overview of the ability of computer simulation in the field of the reactive injection molding process.
RESUMO
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.
RESUMO
According to the 3-phase model, semi-crystalline thermoplastics consist of a mobile amorphous fraction (MAF), a rigid amorphous fraction (RAF), and a crystalline fraction (CF). For the two polyesters Polybutylene Terephthalate (PBT) and Polyethylene Terephthalate (PET), the composition of these phases was investigated using the largest possible variation in the isothermal and non-isothermal boundary conditions. This was performed by combining the conventional Differential Scanning Calorimetry (DSC) with the Fast Scanning Calorimetry (FSC). From the results it can be deduced that the structural composition of both polymers is characterised by a large fraction of the rigid amorphous phase. This is mainly formed either during the primary crystallization in the low temperature range or during the subsequent secondary crystallization that follows primary crystallization in the high temperature range. Depending on the thermal history, the fraction of the mobile amorphous phase of both polymers approaches a minimum, which does not appear to be undercut.
RESUMO
A multiscale simulation method for the determination of mechanical properties of semi-crystalline polymers is presented. First, a four-phase model of crystallization of semi-crystalline polymers is introduced, which is based on the crystallization model of Strobl. From this, a simulation on the nanoscale is derived, which models the formation of lamellae and spherulites during the cooling of the polymer by using a cellular automaton. In the solidified state, mechanical properties are assigned to the formed phases and thus the mechanical behavior of the nanoscale is determined by a finite element (FE) simulation. At this scale, simulations can only be performed up to a simulation range of a few square micrometers. Therefore, the dependence of the mechanical properties on the degree of crystallization is determined by means of homogenization. At the microscale, the cooling of the polymer is simulated by a cellular automaton according to evolution equations. In combination with the mechanical properties determined by homogenization, the mechanical behavior of a macroscopic component can be predicted.
RESUMO
In this study, a novel bio-based flame retardant material consisting of modified vanillin and poly(lactic acid) (PLA) was developed by incorporation of newly discovered additive, bis(5-formyl-2-methoxyphenyl) phenylphosphonate (VP), into the PLA matrix. The chemical structure of VP was confirmed by 1H-, 13C- and 31P NMR and FTIR. The flame retardancy, thermal behavior as well as the mechanical properties of PLA/VP composites were evaluated. With 5 wt% of VP, the LOI of PLA increased from 21.4 to 25.8 and passed the UL-94 V-0 classification. Additionally, the elongation at break was improved from 3% to 11% without sacrificing tensile strength. In an effort to understand the mechanisms, TGA-FTIR, TGA and SEM were performed. This paper suggests a new possibility to prepare polymeric composites with enhanced flame retardancy from sustainable resources.
