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3D Printing of granular biocomposites

自愈水凝胶 材料科学 流变学 3D打印 复合材料 刚度 聚合物 3d打印机 3d打印 复合数 过程(计算) 纳米技术 结构着色 3D生物打印 纳米 仿生学 丝绸 结构材料 极限抗拉强度 天然材料 比索 航程(航空) 高分子科学
作者
Bono, Francesca,Lucherini, Lorenzo,Hirsch, Matteo,Baur, Eva,Amstad, Esther
出处
期刊:
标识
DOI:10.18416/ammm.2023.2309843
摘要

Nature fabricates lightweight materials, such as the mussel byssus or bone, that display a fascinating combination of stiffness and strength. These excellent mechanical properties are a result of an intricate interplay between structural control over the nm up to the mm length scales and locally varying compositions. We are far from reaching a structural and compositional control that can span a similar range of length scales. As a result of the inferior structural and compositional control, most of the manmade polymer-based composites possess mechanical properties that are inferior to those of natural counterparts, especially if normalized by their densities. Bioprinting offers a powerful method to replicate nature’s complexity in synthetic hydrogels. However, rheological modifiers are often required to facilitate the 3D printing process due to the limitations of the rheological properties of single network hydrogel precursor solutions. To expand the range of printable precursor solutions, we introduce microgels, hydrogels formulated as microparticles, to enhance the 3D printability of natural polymer precursor solutions. We reinforce the 3D printed biopolymer-based hydrogels by introducing a secondary network to obtain double network granular hydrogels (DNGHs) [1]. The stiffness of DNGHs can be further increases if they are selectively reinforced with metal-ligand bonds. In the second part of this talk, we will introduce a drop-based process to room temperature 3D print CaCO3-based composites with CaCO3 contents up to 93 wt%, which are much stiffer than the polymer-based composites. These composites display compressive strengths as high as 3.5 MPa. This is achieved by 3D printing bacteria-containing microgels into cm-sized self-supporting granular hydrogels that can subsequently be homogeneously mineralized [2]. Author’s statement Conflict of interest: No conflict of interest to disclose. Animal models: No animal experiment model was used. Informed consent: Informed consent has been obtained from all individuals included in this study. Ethical approval: There is no ethical approval required in this experimental handling. Acknowledgments: NA References [1] Hirsch, M.; Charlet, A.; Amstad, E. 3D Printing of Strong and Tough Double Network Granular Hydrogels. Advanced Functional Materials 2021, 31 (5), 2005929, https://doi.org/10.1002/adfm.202005929. [2] Hirsch, M.; Lucherini, L.; Zhao, R.; Clarà Saracho, A.; Amstad, E. 3D Printing of Living Structural Biocomposites. Materials Today 2023, 62, 21–32. https://doi.org/10.1016/j.mattod.2023.02.001.

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