Origami, the traditional paper art, is a folding technique in which elegant and complex three-dimensional (3D) objects are produced from planar sheets.[1] Significant scientific and technological interest in origami assembly methods have emerged due to the recognition that nature utilizes controlled folding and unfolding schemes to produce intricate architectures ranging from proteins [2] to plants. [3] To date, novel folding pathways have been harnessed to fabricate nanoscale DNA-based objects [4,5] as well as nano-and mesoscale structures, such as 3D metallic objects [6][7][8][9] and silicon solar cells [10] that are lithographically patterned and spontaneously folded via surface tension effects. [11,12] However, the ability to assemble printed structures of arbitrary 3D form, composition, and functionality with the ease, low cost, and versatility of paper origami has not yet been demonstrated. Here, we combine direct-write assembly [13][14][15] with a wet-folding origami technique [16] to create 3D shapes that range from simple polyhedrons to intricate origami forms, which are then transformed to metallic and ceramic structures by thermal annealing. Direct ink writing provides an attractive, non-lithographic approach for meeting the demanding design rules and form factors required for origami-based assembly. In this filamentbased printing method, a concentrated ink is extruded through a tapered cylindrical nozzle that is translated using a three-axis (x-y-z), motion-controlled stage (Fig. 1a). Although this method is capable of printing simple planar and 3D structures from myriad materials, including metallic, [17] ceramic, [18] or polymeric inks, [19,20] it is difficult to pattern high aspect ratio structures without deformation (or slumping) and nearly impossible to directly pattern complex structures with large unsupported regions, such as overhanging features. By combining printing and origami methods, we demonstrate a powerful new approach to overcome such limitations.We first created periodic structures of varying lattice geometry and number of layers by direct-write assembly (Fig. 1b). As one example, we fabricated a 3-layer square lattice (15.4 mm  12.1 mm) composed of stacked linear arrays of ink filaments (diameter, D ¼ 235 mm) aligned with the x-or y-axis, such that their orientation is orthogonal to the previous layer. The square lattices have a center-to-center spacing that varies between 0.5-3 mm, with a typical value of 0.55 mm (top image in Fig. 1b). We also produced two wavy patterns. The first lattice (1-layer, 11 mm  17 mm) consists of a planar array of sinusoidal patterned filaments (D ¼ 258 mm) with a wavelength (l) of
Decomposition of a wood block in sub-and supercritical water was studied by directly observing the change in the size and shape of the wood block in a flow-type reaction cell through sapphire windows attached to the cell. Quantitative kinetic analysis was performed for "hinoki" (a coniferous tree, Chamaecyparis obtusa) as a typical wood sample at a temperature of 523-703 K and a pressure of 10-25 MPa. The phenomenological rate of the size shrink could be analyzed on the basis of two first-order reaction terms. Together with the measurements of the emission of total organic carbons (TOC), it was concluded that the wood block shrank with emitting TOC, and then it shrank at a smaller rate with emitting much smaller amounts of TOC. In the subcritical region, the phenomenological first-order rate constant for the initial shrink increased with the reaction temperature and approximately obeyed the Arrhenius equation with an activation energy of ca. 120 kJ mol -1 . However, the rate constant decreased suddenly near the critical point and again increased with the temperature at the higher temperatures. The phenomenological kinetics was apparently determined by a certain chemical reaction. When the decomposition reaction was assumed to be proton-catalyzed, probably hydrolysis, the rapid change in the vicinity of the critical point was reasonably understood by taking into account the remarkable decrease of the ionic product.
Titanium and its alloys find widespread use in skeletal implants and biomedical devices (e.g., stents and orthodontic applications) owing to their excellent corrosion resistance, bio-compatibility, static and fatigue strength, and lack of magnetism (an important property for magnetic imaging). [1] Microporous titanium provides two additional advantages for implant applications: first, it reduces the stiffness of the material, thus reducing stress shielding, [2,3] and, second, it improves implant anchorage by allowing bone ingrowth. [4][5][6] To date, powder metallurgy approaches have been widely used to create porous Ti structures, through partial sintering, [7][8][9] inclusion of pore formers, [10][11][12][13] expansion of pores pressurized with argon or hydrogen gas, [14,15] or replication of cellular polymers. [16,17] Embrittlement often arises during processing due to the strong chemical affinity of titanium at elevated temperature with atmospheric oxygen, carbon, and nitrogen. Alternate efforts have focused on producing microarchitectured titanium, composed of lattice or truss structures with struts arranged periodically in space. These structures exhibit an outstanding combination of low density, high strength and stiffness, and good damage tolerance. [18] To date, production methods for microarchitectured titanium have focused on replication precision casting, [19,20] sintering of stacked wire arrays, [21] as well as selective electron beam, [22][23][24] or laser [25] sintering of Ti powders.Recently, we introduced a new method for creating 3D microarchitectured Ti structures that combines: [26] (i) direct ink writing (DIW) of planar lattices composed of two layers of orthogonally oriented, patterned TiH 2 filament arrays, followed by (ii) rolling of these pliable lattices into scrolls, or folding into complex three-dimensional shapes, and finally (iii) heat-treating to reduce the hydride to metallic titanium. This new method is characterized by its simplicity, high shape versatility, and ability to control local geometry, as well as scalability to larger structures. [26] Here, we use this novel COMMUNICATION[*] Prof.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.