TY - JOUR A1 - Elsayed, H. A1 - Zocca, Andrea A1 - Schmidt, J. A1 - Günster, Jens A1 - Colombo, P. A1 - Bernardo, E. T1 - Bioactive glass-ceramic scaffolds by additive manufacturing and sinter-crystallization of fi ne glass powders N2 - Wollastonite (CaSiO 3 ) – diopside (CaMgSi 2 O 6 ) glass-ceramic scaffolds have been successfully fabricated using two different additive manufacturing techniques: powder-based 3D printing (3DP) and digital light processing (DLP), coupled with the sinter-crystallization of glass powders with two different compositions. The adopted manufacturing process depended on the balance between viscous flow sintering and crystallization of the glass particles, in turn in fluenced by the powder size and the sensitivity of CaO – MgO – SiO 2 glasses to surface nucleation. 3DP used coarser glass powders and was more appropriate for low temperature firing (800 – 900 °C), leading to samples with limited crystallization. On the contrary, DLP used finer glass powders, leading to highly crystallized glass-ceramic samples. Despite the differences in manufacturing technology and crystallization, all samples featured very good strength-to-density ratios, which bene fit theiruse for bone tissue engineering applications. The bioactivity of 3D-printed glass-ceramics after immersion in simulated body fluid and the similarities, in terms of ionic releases and hydroxyapatite formation with already validated bioactive glass-ceramics, were preliminarily assessed. KW - 3D-Printing KW - Bio Ceramic KW - Additive manufacturing PY - 2018 DO - https://doi.org/10.1557/jmr.2018.120 SN - 2044-5326 SN - 0884-2914 VL - 33 IS - 14 SP - 1960 EP - 1971 PB - Cambridge University Press AN - OPUS4-45718 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Chi, Jinchun A1 - Zocca, Andrea A1 - Agea Blanco, Boris A1 - Melcher, J. A1 - Sparenberg, M. A1 - Günster, Jens T1 - 3D Printing of Self-Organizing Structural Elements for Advanced Functional Structures N2 - A shape evolution approach based on the thermally activated self-organization of 3D printed parts into minimal surface area structures is presented. With this strategy, the present communication opposes currently established additive manufacturing strategies aiming to stipulate each individual volumetric element (voxel) of a part. Instead, a 3D structure is roughly defined in a 3D printing process, with all its advantages, and an externally triggered self-organization allows the formation of structural elements with a definition greatly exceeding the volumetric resolution of the printing process. For enabling the self-organization of printed objects by viscous flow of material, functionally graded structures are printed as rigid frame and melting filler. This approach uniquely combines the freedom in design, provided by 3D printing, with the mathematical formulation of minimal surface structures and the knowledge of the physical potentials governing self-organization, to overcome the paradigm which strictly orrelates the geometrical definition of 3D printed parts to the volumetric resolution of the printing process. Moreover, a transient liquid phase allows local programming of functionalities, such as the alignment of functional particles, by means of electric or magnetic fields. KW - Additive Manufacturing KW - Self-Assembly KW - 3D-Printing KW - Polymeric Materials PY - 2018 DO - https://doi.org/10.1002/admt.201800003 SN - 2365-709X VL - 3 IS - 5 SP - 1800003-1 EP - 1800003-7 PB - Wiley-VCH CY - Weinheim AN - OPUS4-45714 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -