This disclosure is related generally to direct ink writing or 3D printing, and more specifically to shape-shifting structures formed from printed filaments.
Shape-morphing structured materials may have myriad applications in deployable systems, dynamic optics, soft robotics, and medicine, for example. The programming of material shape in three dimensions may require control over the metric tensor at every point in space and time, thus defining how lengths and angles change everywhere. For thin sheets, with in-plane dimensions that are much larger than the thickness, this may be considered to be mathematically equivalent to specifying the first and second fundamental forms of a middle surface that describe how material points deform in the tangent plane and how the middle surface is embedded in three dimensions, allowing for control of both the intrinsic (Gauss) and extrinsic (mean) curvature of the resulting surface. From a physical perspective, this may entail the design of material systems that can expand or contract in response to stimuli such as temperature, humidity, pH, etc., with the capacity to generate and control large in-plane growth gradients combined with differential growth through-thickness, which has thus far proven to be a significant challenge.
A shape-shifting structured lattice comprises a printed lattice including printed ribs joined at nodes. Each printed rib has a predetermined sweep angle {tilde over (θ)}i between adjacent nodes and a bilayer structure including at least two printed filaments in contact along a length thereof. The at least two printed filaments comprise different linear coefficients of thermal expansion and/or different values of elastic modulus. When exposed to a stimulus, the printed lattice adopts a predetermined three-dimensional geometry.
A method of fabricating a shape-shifting structured lattice comprises: conformally mapping a three-dimensional geometry onto a plane to create a planar projection; discretizing the planar projection to create a grid comprising ribs joined at nodes; computing a requisite growth factor based on the three-dimensional geometry and determining a corresponding sweep angle {tilde over (θ)}i between adjacent nodes for each rib, thereby defining a planar print path; depositing filaments along the planar print path to form a printed lattice comprising printed ribs joined at the nodes, each printed rib having the sweep angle {tilde over (θ)}i and a bilayer structure including at least two printed filaments in contact along a length thereof, the at least two printed filaments comprising different ink compositions; curing the different ink compositions; and after the curing, exposing the printed lattice to a stimulus, thereby inducing the printed lattice to adopt the three-dimensional geometry.
A combination of multiple materials and geometry is employed to design a shape-shifting structured lattice that can morph into a predetermined three-dimensional geometry when exposed to a stimulus such as heat. The structured lattice may be formed from printed filaments comprising flow-aligned anisotropic filler particles in polymeric matrices with predetermined crosslink densities. The flow alignment of the anisotropic filler particles may be imparted by extrusion of a precursor ink during direct ink writing of the printed filaments, as described below.
The printed filaments 108a,108b may comprise different linear coefficients of thermal expansion and/or different values of elastic modulus, such that, when exposed to a stimulus, the printed lattice 102 exhibits a shape transformation and adopts a predetermined three-dimensional geometry 110, as illustrated in
Each of the printed filaments 108a,108b comprises a polymer, such as a thermosetting polymer that undergoes a crosslinking process upon curing. The thermosetting polymer may be an elastomer such as silicone (e.g., poly(dimethylsiloxane) (PDMS)) in one example. At least one of the printed filaments 108a,108b may include anisotropic filler particles, in which case the polymer referred to above may function as a polymer matrix. The anisotropic filler particles may have a long axis aligned with the print direction, as discussed below, which may help to reduce thermal expansion of the printed filament(s). The anisotropic filler particles may take the form of glass fibers, oxide fibers, carbon fibers, and/or other suitable fibers. Typically, the anisotropic filler particles may have a length in a range from about 100 microns to 500 microns and a width or diameter in a range from about 1 micron to about 30 microns. The printed filaments 108a,108b may further include other particulate additives, such as metal oxide particles (e.g., silica) or clay particles, which may be incorporated into the precursor ink to impart rheological properties suitable for direct ink writing. The other particulate additives may have a nanoscale particle size, such as a width or diameter in a range from about 5 nm to about 30 nm, or from about 7 nm to about 25 nm. The printed filaments 108a,108b may have a diameter or width in a range from about 10 microns to about 1,000 microns (1 mm), and more typically from about 50 microns to about 500 microns.
Preferably, to ensure that the printed filaments 208a,208b exhibit different linear coefficients of thermal expansion and/or different values of elastic modulus, the printed filaments 208a,208b may be extruded from different precursor inks (“ink compositions”). The ink compositions may be prepared from different uncured (base) polymers and/or different crosslinker-to-base ratios such that the printed filaments 208a,208b comprise different polymer matrices and/or different crosslink densities upon curing. The crosslinker-to-base ratio may lie in a range from about 1:5 to about 1:100, or from about 1:10 to about 1:50. Depending on the ink composition, curing may be effected by exposure to heat, light, and/or a chemical curing agent. Generally speaking, after curing, the printed filaments 208a,208b comprise different linear coefficients of thermal expansion and/or different values of elastic modulus.
In some examples, it may be beneficial to select the same uncured polymer for the different ink compositions while varying the crosslinker-to-base ratio.
As shown in
In some examples, such as that shown in
Referring now to
Referring to
Filaments are deposited along the planar print path to form a printed lattice, as shown in
The printed lattice may then be exposed to a stimulus (e.g., a change in temperature, a change in pH, a change in humidity, a change in pressure, application of a magnetic field, and/or application of an electric field), which induces the printed lattice to adopt the three-dimensional geometry, as shown in
Key parameters of the bilayer structure, the basic functional unit of the shape-shifting structured lattices, are illustrated in
where δκ=κ−{tilde over (θ)} is the change in curvature after ΔT, {tilde over (θ)} is the curvature of the bilayer before ΔT, κ is the curvature after ΔT, t is the layer thickness, β=t1=t2, γ=E1=E2, and subscripts 1 and 2 denote the low and high α materials, respectively.
As in the simple bilayer case, the structured lattices can undergo repeated expansion and contraction in response to a stimulus, such as a change in temperature. The lattice may be homogeneous or heterogeneous, where, in the latter case, the initial sweep angle of each rib is considered an independent degree of freedom and is therefore indexed within the lattice, e.g., {tilde over (θ)}i as opposed to {tilde over (θ)} in the homogeneous case. From a conformal map of the desired target shape to the plane, it is possible to compute the required growth factor for each rib and invert equation (2) to find the corresponding value of {tilde over (θ)}i, as discussed above.
Fabrication of Ink Compositions: Exemplary ink compositions (“inks”) are created by first separately mixing (FlackTek, 120 s at 2000 rpm) the appropriate amount of base and catalyst for two types of PDMS, namely SE 1700 (Dow Corning) with Sylgard 184 (Dow Corning). The neat inks are obtained by combining the resulting pre-mixtures at concentrations of 85% w/w SE 1700 and 15% w/w Sylgard 184, followed by a mixing step (FlackTek, 240 s at 2350 rpm). The filled inks are obtained by combining the SE 1700 and Sylgard 184 pre-mixtures with glass fibers (Fibre Glast, 1/32 inch Glass Fibers, diameter ˜16 μm, length ˜230 μm) at concentrations of 68% w/w SE 1700, 12% w/w Sylgard 184, and 20% w/w glass fibers, followed by a mixing step (FlackTek, 240 sat 2350 rpm). Given the presence of fumed silica in SE 1700 (˜26.5% w/w), the resulting palette of inks contain fumed silica in concentrations ranging from 20% to 22% w/w. As a rheological control, a non-printable mixture (FlackTek, 240 sat 2350 rpm) of 80% w/w Sylgard 184 and 20% w/w of glass fibers is also created. For rheology samples, the crosslinker is replaced with an appropriate concentration of viscosity-matched silicone oils (Sigma Aldrich) to avoid any potential crosslinking effects on the rheological measurements. Notably, the printing process lasts less than ˜90 minutes, much shorter than the 8-hour pot life of the inks. As such, these crosslinking effects do not occur during the printing process. Rheology measurements conducted on the ink compositions show for each a clear plateau modulus, yield stress, and shear thinning response, indicating viscoelasticity. For each ink, the plateau modulus, yield stress, and viscosity exhibit a moderate yet consistent decrease with increasing concentrations of crosslinker. A modest decrease in these parameters is also observed for increasing concentrations of glass fibers.
Fabrication of Printed Lattice: For printing experiments, all ink compositions are loaded into separate 10 cc, Luer-Lok syringes (Nordson, EFD) directly following their synthesis. Upon loading, the inks are then centrifuged (300 s at 3500 rpm for neat inks, and 120 s at 2000 rpm for filled inks) to remove bubbles prior to printing. Each syringe is then mounted to one of four independently controlled z-axes of a multi-axis motion system (ABG 1000, Aerotech Inc.) equipped with a tapered nozzle with a 200 μm inner diameter (Nordson, EFD), and connected to an Ultimus V pressure controller (Nordson, EFD). Custom, open source Python libraries (Mecode) are used to define the print paths of each ink and to coordinate printhead motion with ink extrusion. All samples are printed onto Teflon substrates. Typical pressures and print speeds used are 60 psi and 20 mm/s for the neat inks and 72 psi and 16 mm/s for the filled inks. Generally speaking, a pressure of 50-90 psi and a print speed of 5-50 mm/s may be suitable. For reference, the time it takes to print the lattice for the face, as discussed in reference to
Although the present invention has been described in considerable detail with reference to certain embodiments thereof, other embodiments are possible without departing from the present invention. The spirit and scope of the appended claims should not be limited, therefore, to the description of the preferred embodiments contained herein. All embodiments that come within the meaning of the claims, either literally or by equivalence, are intended to be embraced therein.
Furthermore, the advantages described above are not necessarily the only advantages of the invention, and it is not necessarily expected that all of the described advantages will be achieved with every embodiment of the invention.
The present patent document claims the benefit of priority to U.S. Provisional Patent Application No. 62/749,846, which was filed on Oct. 24, 2018, and is hereby incorporated by reference in its entirety.
This invention was made with government support under grant numbers DMR-1420570 (Harvard MRSEC), 15-33985 (NSF DMREF), and SC001-0000000957 (Charles Stark Draper Laboratory, Inc.) awarded by the National Science Foundation. The government has certain rights in the invention.
Number | Date | Country | |
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62749846 | Oct 2018 | US |