Effect of Chiral Arm Angle on the Stiffness, Auxeticity and Energy Absorption of Polyamide-12 Tetra-Chiral Lattices Under Quasi-Static Compression: A Numerical Baseline Study.
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引用次数: 0
Abstract
Chiral auxetic lattices convert axial loading into node rotation, producing negative Poisson's ratios and high energy absorption. This purely numerical study establishes a quasi-static baseline for additively manufacturable polyamide-12 (PA12) tetra-chiral lattices in which the chiral arm angle (0-90°) is treated as a design variable; no experiments were performed, and the model is verified rather than validated. Geometrically non-linear elastoplastic finite element analyses with a data-sheet-derived bilinear PA12 card and frictional self-contact were carried to 20% nominal strain and supported by mesh convergence, seeded-imperfection and friction sensitivity studies, a full-field lateral-strain measure and a refined sweep at 5° resolution. The arm angle switches the response between a stretch-dominated non-auxetic regime (0°, 50-90°) and a rotation-dominated auxetic regime (15-45°) whose lateral kinematics are not sensitive to mesh density, friction and seeded imperfections. The 15° lattice maximizes stiffness and peak force but is an isolated spike in the refined sweep, exhibits a collapse-mode bifurcation whose branch is selected by the discretization, and reaches the PA12 ductility limit after 3.5 mm of stroke. The 30° architecture sustains 9.4 mm before fracture onset and delivers the highest damage-bounded specific energy absorption of the auxetic window (820 J/kg on the baseline mesh), emerging as the design optimum.
期刊介绍:
Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.