46 research outputs found
The mechanical response of cellular materials with spinodal topologies
The mechanical response of cellular materials with spinodal topologies is
numerically and experimentally investigated. Spinodal microstructures are
generated by the numerical solution of the Cahn-Hilliard equation. Two
different topologies are investigated: "solid models," where one of the two
phases is modeled as a solid material and the remaining volume is void space;
and "shell models," where the interface between the two phases is assumed to be
a solid shell, with the rest of the volume modeled as void space. In both
cases, a wide range of relative densities and spinodal characteristic feature
sizes are investigated. The topology and morphology of all the numerically
generated models are carefully characterized to extract key geometrical
features and ensure that the distribution of curvatures and the aging law are
consistent with the physics of spinodal decomposition. Finite element meshes
are generated for each model, and the uniaxial compressive stiffness and
strength are extracted. We show that while solid spinodal models in the density
range of 30-70% are relatively inefficient (i.e., their strength and stiffness
exhibit a high-power scaling with relative density), shell spinodal models in
the density range of 0.01-1% are exceptionally stiff and strong. Spinodal shell
materials are also shown to be remarkably imperfection insensitive. These
findings are verified experimentally by in-situ uniaxial compression of
polymeric samples printed at the microscale by Direct Laser Writing (DLW). At
low relative densities, the strength and stiffness of shell spinodal models
outperform those of most lattice materials and approach theoretical bounds for
isotropic cellular materials. Most importantly, these materials can be produced
by self-assembly techniques over a range of length scales, providing unique
scalability
A versatile numerical approach for calculating the fracture toughness and R-curves of cellular materials
We develop a numerical methodology for the calculation of mode-I R-curves of
brittle and elastoplastic lattice materials, and unveil the impact of lattice
topology, relative density and constituent material behavior on the toughening
response of 2D isotropic lattices. The approach is based on finite element
calculations of the J-integral on a single-edge-notch-bend (SENB) specimen,
with individual bars modeled as beams having a linear elastic or a power-law
elasto-plastic constitutive behavior and a maximum strain-based damage model.
Results for three 2D isotropic lattice topologies (triangular, hexagonal and
kagome) and two constituent materials (representative of a brittle ceramic
(silicon carbide) and a strain hardening elasto-plastic metal (titanium alloy))
are presented. We extract initial fracture toughness and R-curves for all
lattices and show that (i) elastic brittle triangular lattices exhibit
toughening (rising R-curve), and (ii) elasto-plastic triangular lattices
display significant toughening, while elasto-plastic hexagonal lattices fail in
a brittle manner. We show that the difference in such failure behavior can be
explained by the size of the plastic zone that grows upon crack propagation,
and conclude that the nature of crack propagation in lattices (brittle vs
ductile) depends both on the constituent material and the lattice architecture.
While results are presented for 2D truss-lattices, the proposed approach can be
easily applied to 3D truss and shell-lattices, as long as the crack tip lies
within the empty space of a unit cell.Comment: 40 pages, 14 figure
Mechanical Performance of 3D Printed Interpenetrating Phase Composites with Spinodal Topologies
The mechanical response of interpenetrating phase composites (IPCs) with
stochastic spinodal topologies is investigated experimentally and numerically.
Model polymeric systems are fabricated by Polyjet multi-material printing, with
the reinforcing phase taking the topology of a spinodal shell, and the
remaining volume filled by a softer matrix. We show that spinodal shell IPCs
have comparable compressive strength and stiffness to IPCs with two
well-established periodic reinforcements, the Schwarz P triply periodic minimal
surface (TPMS) and the octet truss-lattice, while exhibiting far less
catastrophic failure and greater damage resistance, particularly at high volume
fraction of reinforcing phase. The combination of high stiffness and strength
and a long flat plateau after yielding makes spinodal shell IPCs a promising
candidate for energy absorption and impact protection applications, where the
lack of material softening upon large compressive strains can prevent sudden
collapse. Importantly, in contrast with all IPCs with periodic reinforcements,
spinodal shell IPCs are amenable to scalable manufacturing via self-assembly
techniques
Catastrophic vs Gradual Collapse of Thin-Walled Nanocrystalline Ni Hollow Cylinders As Building Blocks of Microlattice Structures
Lightweight yet stiff and strong lattice structures are attractive for various engineering applications, such as cores of sandwich shells and components designed for impact mitigation. Recent breakthroughs in manufacturing enable efficient fabrication of hierarchically architected microlattices, with dimensional control spanning seven orders of magnitude in length scale. These materials have the potential to exploit desirable nanoscale-size effects in a macroscopic structure, as long as their mechanical behavior at each appropriate scale â nano, micro, and macro levels â is properly understood. In this letter, we report the nanomechanical response of individual microlattice members. We show that hollow nanocrystalline Ni cylinders differing only in wall thicknesses, 500 and 150 nm, exhibit strikingly different collapse modes: the 500 nm sample collapses in a brittle manner, via a single strain burst, while the 150 nm sample shows a gradual collapse, via a series of small and discrete strain bursts. Further, compressive strength in 150 nm sample is 99.2% lower than predicted by shell buckling theory, likely due to localized buckling and fracture events observed during in situ compression experiments. We attribute this difference to the size-induced transition in deformation behavior, unique to nanoscale, and discuss it in the framework of âsize effectsâ in crystalline strength
Emergence of film-thickness- and grain-size-dependent elastic properties in nanocrystalline thin films
Molecular dynamics simulations of nanocrystalline Ni revealed that the in-plane Youngâs modulus of 2.2 nm grained Ni film with âŒ10 grains across its thickness was only 0.64% smaller than that of bulk, while it dropped to 24.1% below bulk value for âŒ1 grain across film. This size dependence arises from the increased number of more compliant grains adjacent to the free surface. Simulations of nanocrystalline diamond revealed that the anharmonicity of the potential curve determined the sensitivity of the Youngâs modulus to variations in the sample size
Concentration Independent Modulation of Local Micromechanics in a Fibrin Gel
Methods for tuning extracellular matrix (ECM) mechanics in 3D cell culture that rely on increasing the concentration of either protein or cross-linking molecules fail to control important parameters such as pore size, ligand density, and molecular diffusivity. Alternatively, ECM stiffness can be modulated independently from protein concentration by mechanically loading the ECM. We have developed a novel device for generating stiffness gradients in naturally derived ECMs, where stiffness is tuned by inducing strain, while local mechanical properties are directly determined by laser tweezers based active microrheology (AMR). Hydrogel substrates polymerized within 35 mm diameter Petri dishes are strained non-uniformly by the precise rotation of an embedded cylindrical post, and exhibit a position-dependent stiffness with little to no modulation of local mesh geometry. Here we present the device in the context of fibrin hydrogels. First AMR is used to directly measure local micromechanics in unstrained hydrogels of increasing fibrin concentration. Changes in stiffness are then mapped within our device, where fibrin concentration is held constant. Fluorescence confocal imaging and orbital particle tracking are used to quantify structural changes in fibrin on the micro and nano levels respectively. The micromechanical strain stiffening measured by microrheology is not accompanied by ECM microstructural changes under our applied loads, as measured by confocal microscopy. However, super-resolution orbital tracking reveals nanostructural straightening, lengthening, and reduced movement of fibrin fibers. Furthermore, we show that aortic smooth muscle cells cultured within our device are morphologically sensitive to the induced mechanical gradient. Our results demonstrate a powerful cell culture tool that can be used in the study of mechanical effects on cellular physiology in naturally derived 3D ECM tissues
Self calibrating micro-fabricated load cells
Self calibrating micro-fabricated load cells are disclosed. According to one embodiment, a self calibrating load cell comprises a resonant double ended tuning fork force sensor and a phase locked loop circuit for detection of frequency changes upon external load application to the resonant double ended tuning fork force sensor
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Update (2.0) to MiniSurfâA minimal surface generator for finite element modeling and additive manufacturing
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