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Hexagonal Form (hexagonal + form)

Distribution by Scientific Domains
Polymers and Materials Science60%
Chemistry40%

Selected Abstracts

Polymorphic Meniscus Convergence for Construction of Quasi-Periodic Assemblies and Networks of Colloidal Nanoparticles

ADVANCED MATERIALS, Issue 37 2010
Sang-Wook Lee
Quasi-periodic colloidal networks are constructed on the basis of polymorphic meniscus convergence (MC) in an air-cavity-embedded, nano-colloidal system. Depending on the flow associated with the air-cavities, the colloidal particles are self-organized into nanowires through binary MC, Y-junctions through ternary MC, and X-junctions through quaternary MC. The colloidal networks in either square or hexagonal form reflect the flow symmetry according to the air-cavity deformation. [source]

Observation of orientational disorder in the hexagonal stuffed tridymite Sr0.864Eu0.136Al2O4 by the maximum-entropy method

JOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 5 2004
H. Yamada
The crystal structure of a strontium europium aluminate, Sr0.864Eu0.136Al2O4, with a novel hexagonal form was investigated by a combination of Rietveld analysis and the maximum-entropy method (MEM) with synchrotron X-ray powder diffraction data. The electron density image calculated by the MEM/Rietveld method revealed that the apical oxygen ion in the AlO4 tetrahedron has a broad distribution corresponding to an extraordinarily large atomic displacement parameter. This structure could be expressed by a split-atom model, with which the Rietveld refinement gave Rwp = 2.99% and RB = 4.16%. Subsequently, MEM-based pattern fitting (MPF) decreased the R factors to Rwp = 2.81% and RB = 2.34% and the electron density image clearly showed that the apical oxygen ions of the AlO4 tetrahedra are split over three sites around a threefold axis involving an elongated distribution of the residual O ions along the c axis. These results suggest that AlO4 tetrahedra in Sr0.864Eu0.136Al2O4 are orientationally disordered. [source]

Hot Isostatic Pressing of Cubic Boron Nitride,Tungsten Carbide/Cobalt (cBN,WC/Co) Composites: Effect of cBN Particle Size and Some Processing Parameters on their Microstructure and Properties

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2007
V. Martínez
Cubic boron nitride (cBN)-cemented carbide composites have gained attraction over the last few years because of their potential uses as wear parts. The densification behavior of cBN,hard metal composites by glass encapsulation hot isostatic pressing,has been investigated. Composites with different cBN grades (from 0/0.5 to 6/12 ,m particle sizes) and cBN content (up to 50 vol%) were selected for this study. Near-full densification was obtained at temperatures between 1100° and 1200°C, and pressures between 150 and 200 MPa, respectively, while no phase transformation of cBN into the low-hardness hexagonal form has been detected by X-ray diffraction. The addition of cBN to the hard metal base material led to an increase of hardness, a significant increase of fracture toughness (KIC measured by Vickers indentation), and a moderate decrease of mechanical strength (determined by three-point bending). [source]

Influence of the Composition on Crystal Phase and Thermal Behavior of trans -1,4-Butadiene/Isoprene Copolymers

MACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 23 2007
Fabio Bertini
Abstract Butadiene/isoprene copolymers were prepared using the catalyst system V(acac)3 -MAO. The structure of the comonomers is trans -1,4 and the butadiene and isoprene units are statistically distributed along the polymer chain. The attitude of the butadiene sequences to crystallize in the monoclinic form and to evolve in the hexagonal form is preserved in the copolymer for a certain range of composition. The temperature interval between the two endothermic events is progressively reduced by increasing the isoprene content. The monoclinic/hexagonal transition produces a considerable increase in the lamellar thickness of the polymers. Thermal degradation of the copolymers is influenced by the composition and takes place in two different stages: a series of cyclization and cross-linking reactions occur before the decomposition step. [source]

Structure of d(GCGAAAGC) (hexagonal form): a base-intercalated duplex as a stable structure

ACTA CRYSTALLOGRAPHICA SECTION D, Issue 1 2004
d(GCGAAAGC)
A DNA fragment d(GCGAAAGC), postulated to adopt a stable mini-hairpin structure on the basis of its extraordinary properties, has been X-ray analyzed. Two octamers related by a crystallographic twofold symmetry are aligned in an antiparallel fashion and associate to form a duplex, which is maintained by two Watson,Crick G·C base pairs and a subsequent sheared G·A pair at both ends. The central two A residues are free from base-pair formation. The corresponding base moieties of the two strands are intercalated and stacked on each other, forming a long column of G1 -C2 -G3 -A4 -A -A5 -A -G -C -G (asterisks indicate the counter-strand). The Watson,Crick and major-groove sites of the four stacked adenine bases are exposed to the solvent region, suggesting a functional role. Since this structural motif is similar to those found in the nonamers d(GBrCGAAAGCT) and d(GICGAAAGCT), the base-intercalated duplex may be a stable form of the specific sequence. Electrophoresis results suggest that the octamer has two states, monomeric and dimeric, in solution depending on the Mg2+ concentration. The present duplex is preferred under the crystallization conditions, which correspond to physiologically allowed conditions. [source]