Non-isothermal laser-based powder bed fusion (LPBF) of polymers suggests the potential for significantly extending the range of materials applicable for powder-based additive manufacturing of polymers, relying on the absence of a material-specific processing window. To allow for the support-free manufacturing of polymers at a build chamber temperature of 25 °C, applied processing strategies comprise the combination of fractal exposure strategies and locally quasi-simultaneous exposure of distinct segments of a particular cross section for minimizing crystallization-induced part deflection. Based on the parameter-dependent control of emerging cooling rates, formed part morphologies and resulting mechanical properties can be modified. Thermographic in situ measurements allow for correlating thermal processing conditions and crystallization kinetics with component-specific mechanical, morphological, and microstructural properties, assessed ex situ. Part morphologies formed at crystallization temperatures below 70 °C, induced by reduced laser exposure times, are characterized by a nano-spherulitic structure, exhibiting an enhanced elongation at break. An ambient temperature of 25 °C is associated with the predominant formation of a combined (α + γ)-phase, induced by the rapid cooling and subsequent laser-induced tempering of distinct layers, yielding a periodic microstructural evolution. The presented results demonstrate a novel approach for obtaining nano-spherulitic morphologies, enabling the exposure-based targeted adaption of morphological properties. Furthermore, the thermographic inline assessment of crystallization kinetics allows for the enhanced understanding of process-morphology interdependencies in laser-based manufacturing processes of semi-crystalline polymers.

Powder Bed Fusion of Polymers (PBF-LB/P) is a layer-wise additive manufacturing process that predominantly relies on the quasi-isothermal processing of semi-crystalline polymers, inherently limiting the spectrum of polymers suitable for quasi-isothermal PBF. Within the present paper, a novel approach for extending the isothermal processing window towards significantly lower temperatures by applying the quasi-simultaneous laser-based exposure of fractal scan paths is proposed. The proposed approach is based on the temporal and spatial discretization of the melting and subsequent crystallization of semi-crystalline thermoplastics, hence allowing for the mesoscale compensation of crystallization shrinkage of distinct segments. Using thermographic monitoring, a homogenous temperature increase of discrete exposed sub-segments, limited thermal interference of distinct segments, and the resulting avoidance of curling and warping can be observed. Manufactured parts exhibit a dense and lamellar part morphology with a nano-scale semi-crystalline structure. The presented approach represents a novel methodology that allows for significantly reducing energy consumption, process preparation times and temperature-induced material aging in PBF-LB/P while representing the foundation for the processing of novel, thermo-sensitive material systems in PBF-LB/P.

Powder bed fusion of thermoplastic polymers is a powder based additive manufacturing process that allows for manufacturing individualized components with high geometric freedom. Despite achieving higher mechanical properties compared to other additive manufacturing processes, statistical variations in part properties and the occurrence of defects cannot be avoided systematically. In this paper, a novel method for the inline assessment of part porosity is proposed in order to detect and to compensate for inherent limitations in the reproducibility of manufactured parts. The proposed approach is based on monitoring the parameter-specific decay of the optical melt pool radiance during the melting process, influenced by a time dependency of optical scattering within the melt pool. The underlying methodology compromises the regression of the time-dependent optical melt pool properties, assessed in visible light using conventional camera technology, and the resulting part properties by means of artificial neural networks. By applying deep residual neural networks for correlating time-resolved optical process properties and the corresponding part porosity, an inline assessment of the spatially resolved part porosity can be achieved. The authors demonstrate the suitability of the proposed approach for the inline porosity assessment of varying part geometries, processing parameters, and material aging states, using Polyamide 12. Consequently, the approach represents a methodological foundation for novel monitoring solutions, the enhanced understanding of parameter–material interactions and the inline-development of novel material systems in powder bed fusion of polymers.

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Laser-based powder bed fusion (LPBF) of polymers allows for the additive manufacturing of dense components with high mechanical properties. Due to inherent limitations of present material systems suitable for LPBF of polymers and required high processing temperatures, the present paper investigates the in situ modification of material systems using powder blending of p-aminobenzoic acid and aliphatic polyamide 12, followed by subsequent laser-based additive manufacturing. Prepared powder blends exhibit a considerable reduction of required processing temperatures dependent on the fraction of p-aminobenzoic acid, allowing for the processing of polyamide 12 at a build chamber temperature of 141.5 °C. An elevated fraction of 20 wt% of p-aminobenzoic acid allows for obtaining a considerably increased elongation at break of 24.65% ± 2.87 while exhibiting a reduced ultimate tensile strength. Thermal investigations demonstrate the influence of the thermal material history on thermal properties, associated with the suppression of low-melting crystalline fractions, yielding amorphous material properties of the previously semi-crystalline polymer. Based on complementary infrared spectroscopic analysis, the increased presence of secondary amides can be observed, indicating the influence of both covalently bound aromatic groups and hydrogen-bound supramolecular structures on emerging material properties. The presented approach represents a novel methodology for the energy-efficient in situ preparation of eutectic polyamides, potentially allowing for the manufacturing of tailored material systems with adapted thermal, chemical, and mechanical properties.

Additive manufacturing of material systems sensitive to heat degradation represents an essential prerequisite for the integration of novel functionalized material systems in medical applications, such as the hybrid processing of high-performance thermoplastics and gelling polymers. For enabling an inherent process stability under non-isothermal conditions at reduced ambient temperatures in laser-based additive manufacturing, maintaining a homogeneous layer formation is of vital significance. To minimize crystallization-induced deflections of formed layers while avoiding support structures, the temporal and spatial discretization of the melting process is combined with the subsequent quenching of the polymer melt due to thermal conduction. Based on implementing superposed, phase-shifted fractal curves as the underlying exposure structure, the locally limited temporal and spatial discretization of the exposure process promotes a mesoscale compensation of crystallization shrinkage and thermal distortion, enabling the essential homogeneous layer formation. For improving the understanding of local parameter-dependent thermal intra-layer interactions under non-isothermal processing conditions, geometric boundary conditions of distinct exposure vectors and the underlying laser power are varied. Applying polypropylene as a model material, a significant influence of the spatial distance of fractal exposure structures on the thermal superposition of distinct exposure vectors can be derived, implicitly influencing temporal and temperature-dependent characteristics of the material crystallization and the emerging thermal material exposure. Furthermore, the formation of sub-focus structures can be observed, contributing to the spatial discretization of the layer formation, representing a decisive factor that influences the structure formation and mesoscopic part properties in non-isothermal powder bed fusion of polymers. Consequently, the presented approach represents a foundation for the support-free, accelerated non-isothermal additive manufacturing of both polymers and metals, demonstrating a novel methodology for the mesoscale compensation of thermal shrinkage.