共查询到19条相似文献,搜索用时 106 毫秒
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针对国内外火工品、炸药、发射药、推进剂增材制造技术,按照增材制造的技术特点和应用方向,综述了国内外增材制造技术在火炸药成型中的研究现状。概述了材料喷射成型(Material jetting)、材料挤出成型(Material extruding)、光聚合固化技术(Vat photopolymerization)的成型原理、工艺特点及在火炸药成型中的应用情况,介绍了各类增材制造技术中火炸药的物料特性,并对火炸药增材制造技术发展方向进行了预测。指出火炸药增材制造应按照火炸药的应用背景,对增材制造火炸药配方(即耗材)的能量特性、力学特性、能量释放特性及工艺适配性等进行系统研究,以满足不同应用背景的发展需求。附参考文献97篇。 相似文献
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近年来,三维连续网络结构的陶瓷/金属复合材料由于兼具陶瓷材料的耐磨、高强、高硬、抗氧化、耐蚀及钢铁材料的导热性及良好的韧性受到人们的广泛关注。三维连续网络结构的陶瓷/金属复合材料的陶瓷结构的构建是制备复合材料的难题。3D打印技术突破了传统的加工模式,不依赖复杂模具和机械加工,并可根据材料不同的性能要求,开发出不同结构的陶瓷骨架,这将使陶瓷/金属复合材料领域发生巨大变化。本文介绍了陶瓷3D 打印技术的原理、分类、工艺特点及研究进展,并对3D打印技术未来的发展方向进行了展望。 相似文献
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Kylie B. Manning Nicholas Wyatt Lindsey Hughes Adam Cook Nicholas H. Giron Estevan Martinez Christopher G. Campbell Mathias C. Celina 《大分子材料与工程》2019,304(3)
The use of self‐assembling, pre‐polymer materials in 3D printing is rare, due to difficulties of facilitating printing with low molecular weight species and preserving their reactivity and/or functions on the macroscale. Akin to 3D printing of small molecules, examples of extrusion‐based printing of pre‐polymer thermosets are uncommon, arising from their limited rheological tuneability and slow reactions kinetics. The direct ink write (DIW) 3D printing of a two‐part resin, Epon 828 and Jeffamine D230, using a self‐assembly approach is reported. Through the addition of self‐assembling, ureidopyrimidinone‐modified Jeffamine D230 and nanoclay filler, suitable viscoelastic properties are obtained, enabling 3D printing of the epoxy–amine pre‐polymer resin. A significant increase in viscosity is observed, with an infinite shear rate viscosity of approximately two orders of magnitude higher than control resins, in addition to, an increase in yield strength and thixotropic behavior. Printing of simple geometries is demonstrated with parts showing excellent interlayer adhesion, unachievable using control resins. 相似文献
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Transparent alumina ceramics were fabricated using an extrusion-based 3D printer and post-processing steps including debinding, vacuum sintering, and polishing. Printable slurry recipes and 3D printing parameters were optimized to fabricate quality green bodies of varying shapes and sizes. Two-step vacuum sintering profiles were found to increase density while reducing grain size and thus improving the transparency of the sintered alumina ceramics over single-step sintering profiles. The 3D printed and two-step vacuum sintered alumina ceramics achieved greater than 99 % relative density and total transmittance values of about 70 % at 800 nm and above, which was comparable to that of conventional CIP processed alumina ceramics. This demonstrates the capability of 3D printing to compete with conventional transparent ceramic forming methods along with the additional benefit of freedom of design and production of complex shapes. 相似文献
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Minde Jin Markus Stihl Reiner Giesa Christian Neuber Hans-Werner Schmidt 《大分子材料与工程》2021,306(1):2000473
The fourth dimension in 4D printing comprises the ability of materials to recover their shape with time by utilizing 3D printing in combination with shape memory polymers. The focus of this work is on 3D printing of physically crosslinked thermoplastic polymers, which allow a reversible transformation from a temporary to an original shape by an external stimulus temperature, thus realize 4D printing. In this context, (AB)n segmented copolyetherimides consisting of perylene and poly(ethylene glycol) (PEG) segments are synthesized and characterized regarding their thermal and rheological properties in view of 3D printing. The perylene imide segments act as reversible physical crosslinks which disassemble between 100 and 200 °C. The PEG segments exhibit a low melting temperature around 40 to 60 °C and are semi-crystalline at room temperature. The results show that this type of (AB)n segmented copolyetherimide combines reliable 3D printing performance, which is indicated by low warp deformation and excellent interlayer bonding. With a blend of two copolymers, it is able to realize 4D printing. 相似文献
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Alejandro H. Espera Arnaldo D. Valino Jerome O. Palaganas Lucio Souza Qiyi Chen Rigoberto C. Advincula 《大分子材料与工程》2019,304(4)
The need for big volume powder materials in building mechanically robust sintered parts via selective laser sintering (SLS) has been observed considering the direction towards the future of mass fabrication. This work presents a facile approach of combining polyamide‐12 (PA12) and carbon black (CB) powders to be used in the SLS application. The study investigates the mixing consistency, mechanical property, and thermal stability changes of the resulting 3D printed material. Bulk resistivity is correlated with the amount of CB, showing consistency of carbon content in the sintered parts produced by the effective separate grains mixing method. 3D printed parts are built with 0, 1.5, 3, 5 and 10 wt% CB via SLS. Improvements are seen at 1.5 and 3 wt% CB with the blockage of crack growth by the CB particles on applied load. For concentrations greater than 3 wt%, mechanical properties degrade due to hindering of physical contact between PA12 particles caused by CB particles, thereby reducing the effectiveness of the sintering process. The CB/PA12 sintered parts exhibit enhanced thermal stability resulting in higher degradation temperatures than the neat PA12. Therefore, in this study, thermally and mechanically enhanced 3D printed CB/PA12 build parts via SLS are successfully demonstrated. 相似文献
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《大分子材料与工程》2017,302(9)
Additive manufacturing (AM) is still underutilized as an industrial process, but is quickly gaining momentum with the development of innovative techniques and materials for various applications. In particular, stereolithography (SLA) is now shifting from rapid prototyping to rapid manufacturing, but is facing challenges in parts performance and printing speed, among others. This review discusses the application of SLA for polymer nanocomposites fabrication to show the technology's potential in increasing the applicability of current SLA‐printed parts. Photopolymerization chemistry, nanocomposite preparation, and applications in various industries are also explained to provide a comprehensive picture of the current and future capabilities of the technique and materials involved.
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Gianni Pecorini Simona Braccini Gianluca Parrini Federica Chiellini Dario Puppi 《International journal of molecular sciences》2022,23(7)
Polyhydroxyalkanoates are biopolyesters whose biocompatibility, biodegradability, environmental sustainability, processing versatility, and mechanical properties make them unique scaffolding polymer candidates for tissue engineering. The development of innovative biomaterials suitable for advanced Additive Manufacturing (AM) offers new opportunities for the fabrication of customizable tissue engineering scaffolds. In particular, the blending of polymers represents a useful strategy to develop AM scaffolding materials tailored to bone tissue engineering. In this study, scaffolds from polymeric blends consisting of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and poly(D,L-lactide-co-glycolide) (PLGA) were fabricated employing a solution-extrusion AM technique, referred to as Computer-Aided Wet-Spinning (CAWS). The scaffold fibers were constituted by a biphasic system composed of a continuous PHBV matrix and a dispersed PLGA phase which established a microfibrillar morphology. The influence of the blend composition on the scaffold morphological, physicochemical, and biological properties was demonstrated by means of different characterization techniques. In particular, increasing the content of PLGA in the starting solution resulted in an increase in the pore size, the wettability, and the thermal stability of the scaffolds. Overall, in vitro biological experiments indicated the suitability of the scaffolds to support murine preosteoblast cell colonization and differentiation towards an osteoblastic phenotype, highlighting higher proliferation for scaffolds richer in PLGA. 相似文献
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Osman Konuray Arnau Altet Jordi Bonada Agnieszka Tercjak Xavier Fernández-Francos Xavier Ramis 《大分子材料与工程》2021,306(3):2000558
An efficient method to improve the mechanical performance of a commercially available photocure resin is described wherein the resin is modified with a mixture of a cycloaliphatic epoxy and an anhydride curing agent. Photocured samples are thermally treated in a subsequent step to cure the epoxy to obtain an interpenetrated polymer network (IPN) and also complete reaction of the acrylate monomers remaining from the photocure. The latter is accomplished by a thermal radical initiator added earlier into the formulation together with the epoxy-anhydride. The thermal properties and microstructure of the resulting IPN are analyzed. Uniform and quantitative conversions are obtained, with glass transition temperatures comparable to conventional epoxies. The liquid, uncured samples containing different amounts of epoxy are stable at 30 °C for several weeks. In the fully cured epoxy-rich materials, nano-scale phase separation is observed by atomic force microscopy. This is corroborated by the existence of multiple relaxations determined by dynamic mechanical analysis analysis. Specimens from a formulation containing 50% by weight of epoxy-anhydride are 3D printed in a customized masked image processing stereolithography, thermally treated, and are subjected to compression tests. Results show that Young's modulus increases by 900% over the neat resin. 相似文献