Investigations of the carbon fibre cross-sectional areas and their non-circularities by means of laser diffraction

Laser diffraction is a commonly used tool to measure the fibre diameter of carbon fibres prior to mechanical testing. However, non-circularities of carbon fibres need to be considered in order to minimise measuring errors. As the work at hand demonstrates, using a single measurement of the fibre diameter may cause deviations as high as 30% from a computationally determined value. It appears that the error can be minimised by acquiring a data set of several apparent diameters as a function of the angle around the fibre axis. Based on this data, the cross-sectional area can be calculated as a circle with an averaged diameter or as an ellipse by applying an elliptical fitting procedure

Determination of the penetration depth of ceramic blasting particles during composite peening

Composite peening is a process to embed ceramic particles into the surface of materials with the aim to improve the mechanical and tribological properties. These properties depend essentially on the penetration depth of the particles. In order to investigate the penetration depth achieved with composite peening, micrographs were taken and evaluated employing digital image processing. In composite peening, the blasting particles penetrate the surface of the substrate depending on the process parameters. Models from the field of solid particle erosion were applied to predict the penetration depth of the particles. These analytical models can be used to evaluate the influence of specific process parameters on the penetration depth in composite peening. Furthermore, an additional model from ballistics was implemented. A good qualitative agreement was found between the analytical approaches and the experiments regarding the penetration depth after composite peening for the given system. In the future, this will allow estimating the penetration depth for other process parameters and materials for composite peening as well as for issues related to solid particle erosion

Fused filament fabrication: Comparison of methods for determining the interfacial strength of single welded tracks

The mechanical properties of plastic-based additively manufactured specimens have been widely discussed. However, there is still no standard that can be used to determine properties such as the interfacial strength of adjacent tracks and also to exclude the influence of varying manufacturing conditions. In this paper, a proposal is made to determine the interfacial strength using specimens with only one track within a layer. For this purpose, so-called single-wall specimens of polylactide were characterised under tensile load and the interfacial area between the adjacent layers was determined using three methods. It turned out that the determination of the interfacial area via the fracture surface is the most accurate method for determining the interfacial strength. The measured interfacial strengths were compared with the bulk material strength and it was found that the bulk material strength can be achieved under optimal conditions in the FFF process. It was also observed that with increasing nozzle temperature, the simultaneous printing of specimens influences the interfacial strength. To conclude, this method allows to measure the interfacial strength without superimposing the influence of voids. However, for example, the interfacial strength within a layer cannot be determined

Can different parameter sets lead to equivalent optima between geometric accuracy and mechanical properties in Arburg plastic freeforming?

Technological advances have led to the increased use of plastic-based additive manufacturing processes for the production of consumer goods and spare parts. For this reason, the need for the best possible mechanical properties while maintaining geometric accuracy is becoming increasingly important. One of these additive manufacturing processes is the Arburg Plastic Freeforming process, which differs from the widely used Fused Filament Fabrication process in the way that droplets are discharged along a track instead of continuous extruded tracks. As with all other plastic-based additive manufacturing processes, due to the round shape of the tracks, voids occur between the individual tracks during manufacturing, which effects mechanical properties. In contrast to previous work, which mainly focused on how the mechanical properties change with a change in a single printing parameter, this work focused more closely on the interaction of three relevant printing parameters considered as a parameter set. Their influence on the mechanical properties was investigated by tensile tests, the influence on the residual porosity by density measurements and the influence on the geometric accuracy by surface roughness measurements. It was shown that by considering the parameters as a parameter set, states of high density and therefore high mechanical properties while reaching minimal surface roughness can be achieved for significantly more combinations than previously assumed. However, for these states the residual porosity was slightly different. This difference was explained by a parameter-dependent deformation factor of the droplets, which influences the maximal possible degree of filling during manufacturing. For the optimization of arbitrary parameter sets, an analytical model was derived

On the creation and optical microstructure characterisation of additively manufactured foam structures (AMF)

Plastic-based additive manufacturing processes are becoming increasingly popular in the production of structural parts. Based on the idea of lightweight design and the aim of extending the functionality of additive structures, the production of additively manufactured foam structures has emerged as a new field of application. The optical characterisation of these structures is of particular importance for process adjustments and the identification of (unwanted) changes in the foam structure. The degree of foaming and the fineness of a foam structure are of interest at this point. In this context, only the part of a structure dominated by foam pores is considered a foam structure. So far, there are no sophisticated methods for such an optical characterisation. Therefore, in this work, microscope images of manufactured as well as artificially created additively manufactured foam structures were evaluated. On these images, the features porosity, pore size, pore amount and a measure for the textural change were determined in order to obtain information about changes within an additively manufactured foam structure. It is shown that additive structures show changing pore shapes depending on the orientation of the cutting plane, although there are no changes in the foaming behaviour. Therefore, caution is required when identifying changes within the foam structure. It was also found that, owing to the additive process, the total porosity is already set in the slicing process and remains constant even if the degree of foaming of individual tracks is changed. Therefore, the degree of foaming cannot be determined on the basis of the total porosity, but it can be assessed on the basis of the formation of large networks of process-related pores

Compounding of short fiber reinforced phenolic resin by using specific mechanical energy input as a process control parameter

For a newly developed thermoset injection molding process, glass fiber-reinforced phenolic molding compounds with fiber contents between 0 wt% and 60 wt% were compounded. To achieve a comparable remaining heat of the reaction in all compound formulations, the specific mechanical energy input (SME) during the twin-screw extruder compounding process was used as a control parameter. By adjusting the extruder screw speed and the material throughput, a constant SME into the resin was targeted. Validation measurements using differential scanning calorimetry showed that the remaining heat of the reaction was higher for the molding compounds with low glass fiber contents. It was concluded that the SME was not the only influencing factor on the resin crosslinking progress during the compounding. The material temperature and the residence time changed with the screw speed and throughput, and most likely influenced the curing. However, the SME was one of the major influence factors, and can serve as an at-line control parameter for reactive compounding processes. The mechanical characterization of the test specimens revealed a linear improvement in tensile strength up to a fiber content of 40–50 wt%. The unnotched Charpy impact strength at a 0° orientation reached a plateau at fiber fractions of approximately 45 wt%

Development of an injection molding process for long glass fiber-reinforced phenolic resins

Glass fiber-reinforced phenolic resins are well suited to substitute aluminum die-cast materials. They meet the high thermomechanical and chemical demands that are typically found in combustion engine and electric drive train applications. An injection molding process development for further improving their mechanical properties by increasing the glass fiber length in the molded part was conducted. A novel screw mixing element was developed to improve the homogenization of the long fibers in the phenolic resin. The process operation with the mixing element is a balance between the desired mixing action, an undesired preliminary curing of the phenolic resin, and the reduction of the fiber length. The highest mixing energy input leads to a reduction of the initial fiber length L0 = 5000 μm to a weighted average fiber length of Lp = 571 μm in the molded part. This is an improvement over Lp = 285 μm for a short fiber-reinforced resin under comparable processing conditions. The mechanical characterization shows that for the long fiber-reinforced materials, the benefit of the increased homogeneity outweighs the disadvantages of the reduced fiber length. This is evident from the increase in tensile strength from σm = 21 MPa to σm = 57 MPa between the lowest and the highest mixing energy input parameter settings