今日更新:Composite Structures 1 篇,Composites Part A: Applied Science and Manufacturing 1 篇,Composites Part B: Engineering 1 篇
Optimizing fiber paths of tow-steered laminated composites for parametric stability using isogeometric analysis and genetic algorithm
Erfan Shafei, Shirko Faroughi, Timon Rabczuk
doi:10.1016/j.compstruct.2024.117917
基于等几何分析和遗传算法的双向复合材料纤维路径优化
An isogeometric formulation is presented for fiber path optimization of tow-steered composite laminates (TSCL) with minimal parametric instabilities. Here, the fiber path functions of a TSCL is expressed smoothly by Cp−1 continuous non-uniform rational B-splines (NURBS) for engineering shapes, providing accurate field solutions. In this way, the motion equations of a TSCL plate is developed based on the third-order shear deformation theory (TSDT) and the Bolotin’s approximation is used to determine the parametric instability region. Primarily, the accuracy and efficiency of presented framework is measured for a TSCL example with respect to the existing solutions. Then, the optimal fiber paths of TSCL plates are searched using the genetic algorithm (GA) for various geometries, force component combinations, and dynamic-to-static force ratios. Results reveal that the optimal fiber paths are not necessarily symmetric even for regular domains, demonstrating the non-uniform coupling of bending and twisting stiffness in TSCL plates. The optimal design of TSCL fiber paths necessitates the consistency of local stiffness distribution and the resultant bending-twisting mode shape, specially when the dynamic force is high with respect to the static one. Geometry, force component combination, and dynamic-to-static force ratio impose case-specific fiber paths for optimal TSCL plates, requiring both minimal deformation and instability opening.
本文提出了一种等几何计算方法,用于优化纤维路径,使参数不稳定性最小化的牵引复合材料层压板(TSCL)。在这里,TSCL 的纤维路径函数由工程形状的 Cp-1 连续非均匀有理 B 样条(NURBS)平滑表达,提供了精确的现场解。通过这种方法,基于三阶剪切变形理论(TSDT)建立了 TSCL 板的运动方程,并使用博洛廷近似法确定了参数不稳定区域。首先,针对一个 TSCL 例子测量了所提出框架与现有解决方案的 准确性和效率。然后,使用遗传算法(GA)针对各种几何形状、力分量组合和动静力比搜索 TSCL 板的最佳纤维路径。结果发现,即使对于规则域,最佳纤维路径也不一定对称,这表明 TSCL 板中弯曲和扭曲刚度的耦合是不均匀的。TSCL 纤维路径的优化设计要求局部刚度分布和由此产生的弯曲-扭转模态形状保持一致,特别是当动态力相对于静态力较高时。几何形状、力分量组合和动静力比对最佳 TSCL 板的纤维路径提出了具体要求,既要变形最小,又要消除不稳定性。
Stochastic properties of strains of randomly-oriented chopped strand composites under unidirectional loading
Hiroshi Suemasu, Takashi Murakami, Tsuyoshi Matsuo
doi:10.1016/j.compositesa.2024.108028
单向载荷下随机取向短切链复合材料应变的随机特性
Randomly-oriented chopped strand composite (ROS) specimens were tested under unidirectional load, and the results were statistically treated as the material properties of ROS composites varying across specimens. The strain fields were measured using digital image correlation (DIC). To evaluate the elastic properties quantitatively from the experimentally measured in-plane strain data, the probabilistic properties of the strain were obtained and investigated. The average and standard deviation, probabilistic density function and spatial autocorrelation function, were obtained to determine an appropriate test method and data treatment rules to thoroughly understand the elastic properties of the ROS composites. Assuming spatial ergodicity, the statistical quantities of the strains were determined from sample averages and spatial averages simultaneously. Reasonable test conditions, such as the number and sizes of specimens, gauge sections, data measurement, and analysis procedures for appropriately determining the elastic performance, were discussed through statistical quantities of the strain.
在单向载荷作用下对随机定向切链复合材料(ROS)试样进行测试,并将测试结果统计为不同试样间ROS复合材料性能的差异。采用数字图像相关(DIC)技术测量应变场。为了从实验测量的面内应变数据中定量评价弹性性能,得到并研究了应变的概率特性。通过得到平均和标准差、概率密度函数和空间自相关函数,确定合适的测试方法和数据处理规则,从而全面了解ROS复合材料的弹性性能。假设空间遍历性,菌株的统计量同时由样本平均值和空间平均值确定。通过应变的统计量,讨论了合理的试验条件,如试样的数量和尺寸、测量截面、数据测量以及适当确定弹性性能的分析程序。
Dual microparticles programmed delivery system regulating stem cell-based cartilage regeneration by cartilage-specific matrix hydrogels
Xinyue Ran, Qianyi Wang, Yuyan Sun, Qingqing Pan, Hongying Chen, Wenjie Ren, Yingying Huo, Ying Zhang, Yujie Hua, Guangdong Zhou, Xiaoyun Wang
doi:10.1016/j.compositesb.2024.111221
双微粒子程序传递系统调节软骨特异性基质水凝胶干细胞软骨再生
Bone marrow mesenchymal stem cells (BMSCs)-based engineered cartilage usually faces the significant challenge of endochondral ossification tendency in an ectopic environment because of the inevitable vascular infiltration during chondrogenic differentiation and developmental stages. Additionally, current scaffold-free BMSC cartilage regeneration requires a long in vitro preinduction time for chondrogenic differentiation before in vivo transplantation, which limits its application in multiple cartilage defect repair. Therefore, ideal stem cell-based cartilage regeneration needs to meet time-dependent requirements of both early chondrogenic and late anti-angiogenic microenvironments in vivo. Here, we developed a cartilage-specific matrix hydrogel (CMH) with a dual microparticle-based programmed delivery system (dM-PDs) to dynamically regulate in vivo stem cell-based cartilage regeneration without in vitro preinduction. In this study, CMH scaffolds offer a three-dimensional matrix microenvironment for tissue regeneration, while dM-PDs has an early chondrogenic induction function to promote cartilage-specific differentiation and exerts a late anti-angiogenic effect to stabilize the cartilaginous phenotype. Stem cell-based cartilage regeneration was successfully achieved by sequentially dynamic regulation in vivo by dM-PDs, in which TGFβ3-loaded microparticles effectively activated the early-stage TGFβ/Smad signaling pathway and levatinib-loaded microparticles regulated the late-stage VEGF/TIMP signaling pathway. This study demonstrates a universal stem cell-based cartilage regeneration technique for clinical cartilage defects repair.
基于骨髓间充质干细胞(BMSCs)的工程软骨在异位环境中由于软骨分化和发育阶段不可避免的血管浸润而面临软骨内成骨倾向的重大挑战。此外,目前无支架的BMSC软骨再生在体内移植前需要较长的体外预诱导成软骨分化时间,这限制了其在多发性软骨缺损修复中的应用。因此,理想的干细胞软骨再生需要同时满足体内早期软骨形成和晚期抗血管生成微环境的时间依赖性要求。在这里,我们开发了一种软骨特异性基质水凝胶(CMH),它具有双微颗粒为基础的程序传递系统(dm - pd),可以动态调节体内基于干细胞的软骨再生,而无需体外预诱导。本研究中,CMH支架为组织再生提供了三维基质微环境,dm - pd具有促进软骨特异性分化的早期成软骨诱导功能,并具有稳定软骨表型的晚期抗血管生成作用。通过dm - pd在体内的连续动态调控,成功实现了基于干细胞的软骨再生,其中负载tgf - β3的微颗粒有效激活早期tgf - β/Smad信号通路,负载levatinib的微颗粒调节晚期VEGF/TIMP信号通路。本研究展示了一种通用的基于干细胞的软骨再生技术用于临床软骨缺损修复。