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Honeycomb Structures (honeycomb + structure)
Selected AbstractsMicrostructure and Properties of SiC Honeycomb StructuresADVANCED ENGINEERING MATERIALS, Issue 12 2008D. Galsterer In this work, a novel processing route was used for fabrication of porous beta-SiC materials below 1450,°C. Honeycomb structures, based on Si, C and Al, were extruded and afterwards converted into SiC based ceramics at temperatures between 1050,°C and 1450,°C in Ar atmosphere. A conversion temperature below 1450,°C was applied due to the low melting point of the used Si-Al-alloy. [source] Self-Organized Single-Walled Carbon Nanotube Conducting Thin Films with Honeycomb Structures on Flexible Plastic FilmsADVANCED FUNCTIONAL MATERIALS, Issue 2 2009Nobuo Wakamatsu Abstract Complex 1, synthesized from anionic shortened single-walled carbon nanotubes and cationic ammonium lipid dissolved in organic solvents, is cast on pretreated transparent flexible poly(ethylene terephthalate) (PET) films under a higher relative humidity to form thin films with self-organized honeycomb structures. The cell sizes are controllable by changing the experimental conditions. The lipid, which is the cationic part of complex 1, is easily removed by a simple ion-exchange method, while maintaining the basic honeycomb structures. After the ion exchange, the nanotube honeycomb films on PET with thinner skeletons exhibit a dramatic decrease in the surface resistivity from insulating to conducting. Carbon nanotubes with honeycomb structures formed by the self-organization on flexible polymer films are useful in many areas of nanoscience and technology including nanomaterials, nanoelectronics, nanodevices, catalysts, sensors, and so on. [source] Supramolecular Chemistry Based on [W3S4(H2O)6Cl3]+ , A Versatile Building BlockEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 1 2004Maxim N. Sokolov Abstract The cluster [W3S4(H2O)6Cl3]+ (which is present in solutions of [W3S4(H2O)9]4+ in 1,4 M HCl) reacts with the macrocyclic cavitand cucurbituril (C36H36N24O12) to form supramolecular adducts of 2:1 cluster/cucurbituril stoichiometry, where two portals of cucurbituril (which contains a water molecule in its cavity) are closed by two cluster cations. These aggregates are bound together in the solid by complementary hydrogen bonds between coordinated Cl, and the cations H9O4+ to give chains. Thus, a supramolecular architecture is achieved from three different but complementary building blocks. The packing of the chains affords a honeycomb structure (hexagonal symmetry) with channels (about 5.2 Ĺ in diameter). The overall stoichiometry is (H9O4){[W3S4(H2O)6Cl3]2(C36H36N24O12)}Cl3·16.15H2O (1). [W3S4(H2O)6Cl3]+ reacts with SbCl3 in 6 M HCl to give cuboidal [W3(SbCl3)S4(H2O)6Cl3]+, which forms with the macrocyclic cavitand cucurbituril a 2:1 cluster/cucurbituril adduct , a discrete supramolecule consisting of five independent molecular units. In the solid it crystallizes as a salt of very rare anion [SbCl6]3, with the stoichiometry {[W3(SbCl3)S4(H2O)6Cl3]2(C36H36N24O12)}(SbCl6)2/3·12H2O (2). (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source] Deposition of Functionalized Cr7Ni Molecular Rings on Graphite from the Liquid PhaseADVANCED FUNCTIONAL MATERIALS, Issue 10 2010Alberto Ghirri Abstract Graphite is a clean substrate and its nanostructures hold great potential for applications. Anchoring large molecules on graphite represents a challenge for several reasons that essentially rise from the planar bonds of the packed honeycomb structure of carbon. Here, a systematic investigation by AFM and XPS on different derivatives of molecular Cr7Ni rings deposited on highly oriented pyrolytic graphite (HOPG) is reported. Cr7Ni is emerging as a prototipical example of molecular antiferromagnet on which quantum phenomena and coherence have been demonstrated. For the deposition of Cr7Ni on HOPG, two strategies are adopted: 1) Cr7Ni rings are functionalized with extended alkyl/benzene terminations and 2) a self-assembled monolayer of alkyl chains with sulfonate terminations is deposited and then a cationic Cr7Ni derivative is used. In both cases the electronic bond with the carbon surface is soft, but the two-step procedure is efficient, albeit indirect, in sticking molecular Cr7Ni on HOPG. These strategies can be easily extended to deposit other complex molecular aggregates on graphite from the liquid phase. [source] Solvent Resistant Honeycomb Films from Photo-Crosslinkable PolycinnamateMACROMOLECULAR RAPID COMMUNICATIONS, Issue 8 2007Olaf Karthaus Abstract Microporous films consisting of two-dimensionally ordered void structures - so-called honeycomb films - were produced by evaporation of polymer solutions under high humidity. Two types of poly(vinyl cinnamate)s were used: A newly synthesized amphiphilic poly(vinyl cinnamate) and a mixture of a commercial poly(vinyl cinnamate) and an amphiphilic polyion complex. Photo-crosslinking of the honeycomb structure could be achieved by UV irradiation while completely retaining the film morphology. The crosslinked films showed excellent stability against organic solvents. [source] Microstructures of metal grains in ordinary chondrites: Implications for their thermal historiesMETEORITICS & PLANETARY SCIENCE, Issue 3 2000Hugues LEROUX Three ordinary chondrites, Saint Séverin (LL6), Agen (H5), and Tsarev (L6) were selected because they display contrasting microstructures, which reflects different thermal histories. In Saint Séverin, the microstructure of the Ni-rich metal grains is due to slow cooling. It consists of a two-phase assemblage with a honeycomb structure resulting from spinodal decomposition similar to the cloudy zone of iron meteorites. Microanalyses show that the Ni-rich phase is tetrataenite (Ni = 47 wt%) and the Ni-poor phase, with a composition of ,25% Ni, is either martensite or taenite, these two occurring adjacent to each other. The observation that the Ni-poor phase is partly fcc resolves the disagreement between previous transmission electron microscopy (TEM) and Mössbauer studies on iron meteorites and ordinary chondrite metal. The Ni content of the honeycomb phase is much higher than in mesosiderites, confirming that mesosiderites cooled much more slowly. The high-Ni tetrataenite rim in contact with the cloudy zone displays high-Ni compositional variability on a very fine scale, which suggests that the corresponding area was destabilized and partially decomposed at low temperature. Both Agen and Tsarev display evidence of reheating and subsequent fast cooling obviously related to shock events. Their metallic particles mostly consist of martensite, the microstructure of which depends on local Ni content. Microstructures are controlled by both the temperature at which martensite forms and that at which it possibly decomposes. In high-Ni zones (>15 wt%), martensitic transformation started at low temperature (<300 °C). Because no further recovery occurred, these zones contain a high density of lattice defects. In low-Ni zones (<15 wt%), martensite grains formed at higher temperature and their lattice defects recovered. These martensite grains present a lath texture with numerous tiny precipitates of Ni-rich taenite (Ni = 50 wt%) at lath boundaries. Nickel composition profiles across precipitate-matrix interfaces show that the growth of these precipitates was controlled by preferential diffusion of Ni along lattice defects. The cooling rates deduced from Ni concentration profiles and precipitate sizes are within the range 1,10 °C/year for Tsarev and 10,100 °C/year for Agen. [source] Microstructured horizontal alumina pore arrays as growth templates for large area few and single nanowire devicesPHYSICA STATUS SOLIDI - RAPID RESEARCH LETTERS, Issue 2 2008Ying Xiang Abstract We demonstrate the fabrication of horizontally aligned and well-defined nanopore structures by anodic oxidation of aluminum thin films and micro stripes on a Si substrate. We are able to control both, the pore diameters and interpore distances from 10 nm to 130 nm and from 30 nm to 275 nm, respectively. The anisotropy of the system induces some deviations in the pore configuration from the typical honeycomb structure. By decreasing the dimensions of the Al structures, the final pore diameter and interpore distance remains constant, enabling the transition from multiple to a few nanowire porous structures. Finally, we successfully filled the nanopores by pulsed electroplating, as demonstrated both by Scanning Electron Microscopy and by current,voltage measurements. Having full control over the size, the density, the position and the orientation of the porous structure, our approach is promising for many exciting applications, including nanoelectronics and sensing. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Fabrication of Ordered Nanostructured Arrays Using Poly(dimethylsiloxane) Replica Molds Based on Three-Dimensional Colloidal CrystalsADVANCED FUNCTIONAL MATERIALS, Issue 10 2009Hong Kyoon Choi Abstract Hexagonally arrayed structures of colloidal crystals with uniform surface are a good candidate for master molds to be used in soft lithography. Here, the fabrication of periodically arrayed nanostructures using poly(dimethylsiloxane) (PDMS) molds based on three-dimensionally (3D) ordered colloidal crystals is reported. A robust, high-quality 3D colloidal-crystal master molds is prepared using the colloidal suspension containing a water-soluble polymer. The surface patterns of the 3D colloidal crystals can then be transferred onto a polymer film via soft lithography, by means of the replication of the surface pattern with PDMS. Various hexagonally arrayed nanostructure patterns can be fabricated, including close-packed and non-close-packed 2D arrays and honeycomb structures by the structural modification of the 3D colloidal-crystal templates. The replicated hexagonally arrayed structures can also be used as templates for producing colloidal crystals with 2D superlattices. [source] Self-Organized Single-Walled Carbon Nanotube Conducting Thin Films with Honeycomb Structures on Flexible Plastic FilmsADVANCED FUNCTIONAL MATERIALS, Issue 2 2009Nobuo Wakamatsu Abstract Complex 1, synthesized from anionic shortened single-walled carbon nanotubes and cationic ammonium lipid dissolved in organic solvents, is cast on pretreated transparent flexible poly(ethylene terephthalate) (PET) films under a higher relative humidity to form thin films with self-organized honeycomb structures. The cell sizes are controllable by changing the experimental conditions. The lipid, which is the cationic part of complex 1, is easily removed by a simple ion-exchange method, while maintaining the basic honeycomb structures. After the ion exchange, the nanotube honeycomb films on PET with thinner skeletons exhibit a dramatic decrease in the surface resistivity from insulating to conducting. Carbon nanotubes with honeycomb structures formed by the self-organization on flexible polymer films are useful in many areas of nanoscience and technology including nanomaterials, nanoelectronics, nanodevices, catalysts, sensors, and so on. [source] Lithographically Patterned Breath Figure of Photoresponsive Small Molecules: Dual-Patterned Honeycomb Lines from a Combination of Bottom-Up and Top-Down LithographyADVANCED MATERIALS, Issue 41 2009Jung Hak Kim A line-patterned breath figure film is achieved using a photo-crosslinkable small molecule through a novel dual-patterning process that combines a breath-figure technique (bottom-up) and photolithography (top-down). The organogelator molecules form honeycomb structures, organizing into supramolecular fibers similar to polymers that stabilize water droplets. [source] Effect of Slurry Rheological Properties on the Coating of Ceramic Honeycombs with Yttria-Stabilized-Zirconia WashcoatsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 5 2000Christos Agrafiotis Recently, a novel automotive catalyst design, based on the use of palladium supported on yttria-stabilized zirconia (YSZ), was proposed. In the present work, the coating of cordierite honeycomb samples with YSZ slurries for the preparation of such washcoats was investigated. The loading percentage, homogeneity, and reproducibility were found to depend strongly on the slurry viscosity. Parameters such as the slurry-solids content, pH, type of powder used, and use and quantity of the dispersants were optimized for the preparation of stable, low-viscosity YSZ slurries, adjustments that could lead to an efficient coating process for honeycomb structures. [source] Convergence in the macroscopic anatomy of the reticulum in wild ruminant species of different feeding types and a new resulting hypothesis on reticular functionJOURNAL OF ZOOLOGY, Issue 1 2010M. Clauss Abstract The reticulum is the second part of the ruminant forestomach, located between the rumen and the omasum and characterized by honeycomb-like internal mucosa. With its fluid contents, it plays a decisive role in particle separation. Differences among species have been linked to their feeding style. We investigated whether reticulum size (absolute and in relation to rumen size) and size of the crests that form the mucosal honeycomb pattern differ among over 60 ruminant species of various body sizes and feeding type, controlling for phylogeny. Linear dimensions generally scaled allometrically, that is to body mass0.33. With or without controlling for phylogeny, species that ingest a higher proportion of grass in their natural diet had both significantly larger (higher) rumens and higher reticular mucosa crests, but neither reticulum height nor reticulum width varied with feeding type. The height of the reticular mucosa crests represents a dietary adaptation in ruminants. We suggest that the reticular honeycomb structures do not separate particles by acting as traps (neither for small nor for large particles), but that the structures reduce the lumen of the reticulum during contractions , at varying degrees of completeness in the different feeding types. In browsing species with rumen contents that may be less fluid and more viscous than those of the reticulum, incomplete closure of the lumen may allow the reticulum to retain the fluid necessary for particle separation. In grazing species, whose rumen contents are more stratified with a larger distinct fluid pool, a more complete closure of the reticular lumen due to higher crests may be beneficial as the reticulum can quickly re-fill with fluid rumen contents that contain pre-sorted particles. [source] New Polymeric Materials with Interferential Optical PropertiesMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 13 2007Leďla Ghannam Abstract Nature provides a wide pallet of colors but also a wide number of fascinating optical phenomena such as nacre or interferential effects, which can be observed in insect wings and shellfish. The origin of such effects is attributed to the presence of highly ordered arrangements in Nature's materials. The aim of this paper is to focus some new approaches and advances for creating interferential optical phenomena as observed in nature by tuning or modeling the polymer architectures or organization. A relatively simple method is described to prepare organic/inorganic hybrid pigments constituted of mica platelets and adsorbed polymer layers. It is shown that the color of mica is changed upon polymer adsorption, and when one of the copolymer sequences includes a dye, its color is influenced by the chemical properties of the mica surface. Moreover, a new facile route is presented to obtain highly ordered surfaces using ionomer macromolecular designs synthesized in one step by controlled radical polymerization. The preparation of films with very regular pore size and spatial organization is successfully realized by using ionomer solutions. An original property of these films with an iridescent color obtained by light diffraction as a result of the optical interferences of sunlight with the periodic honeycomb structures is presented. All these new materials based on polymeric controlled structures can reproduce nature by creating an optical interferential and iridescent material, which offers new fascinating applications as original bio-mimetic materials on inorganic surfaces. [source] |