In this study, the feasibility of co-grinding and the subsequent thermal rounding to produce spherical polymer blend particles for selective laser sintering (SLS) is demonstrated for polybutylene terephthalate (PBT) and polycarbonate (PC). The polymers are jointly comminuted in a planetary ball mill, and the obtained product particles are rounded in a heated downer reactor. The size distribution of PBT–PC composite particles is characterized with laser diffraction particle sizing, while the shape and morphology are investigated via scanning electron microscopy (SEM). A thorough investigation and characterization of the polymer intermixing in single particles is achieved via staining techniques and Raman microscopy. Furthermore, polarized light microscopy on thin film cuts enables the visualization of polymer mixing inside the particles. Trans-esterification between PBT and PC during the process steps is investigated via vibrational spectroscopy and differential scanning calorimetry (DSC). In this way, a new process route for the production of novel polymer blend particle systems for SLS is developed and carefully analyzed.

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Powder flowability is key to achieving high process stability and part quality by application of smooth and dense layers in selective laser sintering (SLS). This study sheds light on the rarely investigated effect of tribo-electric charge build-up during powder delivery in the SLS process. This is achieved by a novel approach to quantify electrostatic potentials during doctor blading. The presented model setup is used in combination with charge spectrometry and impedance spectroscopy to investigate the alterations in tribo-electric charging behavior for the most commonly used laser sintering material polyamide 12 in its virgin and aged, c.f. reused, states. We show that the electrostatic charge build-up is significantly enhanced for aged polymer powder material, likely contributing to altered performance in SLS processing.

Polypropylene (PP) powders are coated with silica nanoparticles in a fluidized bed to improve the flow behavior of the powders and the processability in powder bed fusion. The nanoparticles are produced in situ via dusty plasma‐enhanced chemical vapor deposition (PECVD) in an atmospheric‐pressure Ar/O2 plasma jet fixed at the distributor plate of the fluidized bed. Hexamethyldisiloxane is used as a precursor of the nanoparticles. The influence of the oxygen concentration in the plasma gas and the number of treatment cycles on the chemical composition of the nanoparticles, the amount of nanoparticles deposited, and the flow properties of the coated PP powders is investigated. The chemical composition of the formed silica particles is determined by X‐ray photon spectroscopy and infrared spectroscopy. The results reveal that the composition of the nanoparticles is SiOxCy, that is, the portion of organic residues introduced by the precursor can be controlled by changing the oxygen concentration in the plasma gas. The mass of nanoparticles deposited on the polymer powder's surface, as determined by inductively coupled optical emission spectroscopy, shows a linear dependence of the number of cycles and the oxygen concentration in the plasma gas. A considerable improvement of the flow behavior of the PP powders is observed after PECVD treatment.