Search results for "MINERALOGY"

showing 10 items of 1516 documents

Comparative study of polar perovskite surfaces

2004

A novel model of the ‘‘zig–zag’’ (1 1 0) polar surface termination of ABO3 perovskites is suggested and analyzed. Classical shell model calculations for BaTiO3, SrTiO3 and LaMnO3 show that such the (1 · 2) (1 1 0) surface reconstruction has the lowest energy, comparable to that for the (1 0 0) surfaces. The calculated surface energy reaches the saturation only when 6–8 atomic near-surface planes are allowed to relax. Surface relaxation leads to the formation of considerable dipole moment perpendicular to the surface. The predicted surface polarization of thin perovskite films, even in the cubic phase, could affect their dielectric properties. � 2004 Elsevier B.V. All rights reserved.

Materials scienceMineralogySurfaces and InterfacesDielectricSurface finishCondensed Matter PhysicsMolecular physicsSurface energySurfaces Coatings and FilmsDipolechemistry.chemical_compoundchemistryMaterials ChemistryStrontium titanateSurface reconstructionPerovskite (structure)Surface statesSurface Science
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Precursor-based synthetic pathways to nanometer NdNiO3−x particles

1993

Abstract The oxygen deficient neodymium nickel perovskite, NdNiO3−x, has been obtained by different low temperature-low oxygen pressure synthetic procedures. Besides a solid-matrix based route, both ordered and disordered chemical-precursors have been used as starting products. X-ray powder diffraction shows that the structure of this defective perovskite is orthorhombic. The study of the grain morphology of the products as resulting from the different synthetic procedures indicates that the main parameter determining the average particle size, which is in the nanometer range, is the maximum temperature achieved in the synthesis. Resistivity and DSC measurements show the existence of a meta…

Materials scienceMineralogychemistry.chemical_elementInsulator (electricity)General ChemistryCondensed Matter PhysicsNeodymiumNickelchemistryChemical engineeringElectrical resistivity and conductivityGeneral Materials ScienceOrthorhombic crystal systemNanometreParticle sizePowder diffractionSolid State Ionics
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Low-temperature Ti-containing 3:2 and 2:1 mullite nanocrystals from single-phase gels

2007

Abstract TiO 2 -containig single-phase gels with (Al 2 O 3  + TiO 2 )/(SiO 2 ) molar ratios 3/2 and 2/1 were prepared by gelling mixtures of aluminium nitrate, tetraethylorthosilicate and titanium isopropoxide. Gels were fast heated at several temperatures up to 1100 °C. Dried and heated gels were characterized by differential thermal analysis (DTA), magic angle spinning nuclear magnetic resonance (MAS-NMR), X-ray powder diffraction (XRD), and scanning and transmission electron microscopies (SEM and TEM). Coupled DTA and XRD results of gels fast heated at 900 °C showed the crystallisation of two mullites as well as a small amount of alumina-silica spinel. 27 Al NMR spectra showed the format…

Materials scienceMineralogychemistry.chemical_elementMulliteAluminium nitratelaw.inventionchemistry.chemical_compoundchemistryChemical engineeringlawAluminiumDifferential thermal analysisMaterials ChemistryCeramics and CompositesMagic angle spinningCrystallizationTitanium isopropoxidePowder diffractionJournal of the European Ceramic Society
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MCM-41, MCM-48 and related mesoporous adsorbents: their synthesis and characterisation

2001

MCM-41, MCM-48, MCM-41 analogue materials and disordered silica xerogels were compared with respect to their long range and short range order, their specific surface area, pore structure and pore structural parameters, pore wall thickness and their surface hydroxyl group concentration. Based on X-ray diffraction data it could be seen that the degree of long range order decreased in the order MCM-41>MCM-48>MCM-41 analogues >amorphous silica xerogels. The particle porosity and pore wall thickness increased in the same sequence such that MCM-41 analogues and amorphous silica xerogels were more stable towards water and water vapour. The concentration of the surface hydroxyl groups increased whe…

Materials scienceMineralogylaw.inventionColloid and Surface ChemistryAdsorptionChemical engineeringMCM-41lawSpecific surface areaParticleCalcinationMesoporous materialPorosityWater vaporColloids and Surfaces A: Physicochemical and Engineering Aspects
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Porous organic cage compounds as highly potent affinity materials for sensing by quartz crystal microbalances.

2012

Porosity makes powerful affinity materials for quartz crystal microbalances. The shape-persistent organic cages and pores create superior affinity systems to existing ones for direct tracing of aromatic solvent vapors. A shape and size selectivity for the analytes is observed. These organic cages can be processed to thin films with highly reproducible sensing properties.

Materials scienceMiniaturizationMechanical EngineeringMineralogyQuartz crystal microbalanceEquipment DesignMicro-Electrical-Mechanical SystemsHydrocarbons AromaticCondensed Matter::Soft Condensed MatterCrystalEquipment Failure AnalysisAromatic solventChemical engineeringMechanics of MaterialsSize selectivityPhysics::Atomic and Molecular ClustersGeneral Materials ScienceGasesPhysics::Chemical PhysicsThin filmOrganic ChemicalsPorosityQuartzPorosityAdvanced materials (Deerfield Beach, Fla.)
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Large monolithic silica-based macrocellular foams with trimodal pore system.

2003

Silica-based materials with hierarchical pore systems at three different length scales (small mesopores–large mesopores–macropores) have been prepared through a nanotectonic approach by using mesoporous nanoparticles as building blocks; the resulting materials present a highly accessible foam-like architecture and can be prepared as large monoliths. Huerta Morillo, Lenin Jose, Lenin.Huerta@uv.es ; Latorre Saborit, Julio, Julio.Latorre@uv.es ; Beltran Porter, Aurelio, Aurelio.Beltran@uv.es ; Beltran Porter, Daniel, Daniel.Beltran@uv.es ; Amoros del Toro, Pedro Jose, Pedro.Amoros@uv.es

Materials scienceMonolithic silica-based ; Trimodal pore system ; Different length scalesUNESCO::QUÍMICAMetals and AlloysNanoparticleMineralogyPore systemGeneral ChemistryUNESCO::QUÍMICA::Química macromolecular:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineeringMaterials ChemistryCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]Trimodal pore systemMesoporous materialDifferent length scalesMonolithic silica-basedChemical communications (Cambridge, England)
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Particle size and morphology control of the negative thermal expansion material cubic zirconium tungstate

2009

Cubic ZrW2O8 is a negative thermal expansion (NTE) material that is of interest as filler in controlled thermal expansion composites. It is easily accessible from a hydrated precursor, ZrW2O7(OH)2·2H2O, which can be obtained by hydrothermal synthesis. Different reaction conditions were investigated to gain control over the morphology, and to minimize the particle size. Optimized procedures resulted in rod-shaped particles with widths of 10–30 nm and lengths of 200–500 nm, which showed little agglomeration. The particle size and morphology of the precursor are preserved during conversion to the NTE phase at 600–650 °C.

Materials scienceMorphology (linguistics)MineralogyZirconium tungstateGeneral ChemistryMicrostructureThermal expansionchemistry.chemical_compoundChemical engineeringNegative thermal expansionchemistryPhase (matter)Materials ChemistryHydrothermal synthesisParticle sizeJournal of Materials Chemistry
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Morphology and transport parameters of cold-rolled low-density polyethylene

1986

Abstract Sheets of low-density polyethylene were rolled at room temperature. Samples with two different degrees of rolling were obtained. The structural changes induced by the rolling treatments were investigated using scanning electron microscopy and by analyzing the transport properties. Results suggest that in the analyzed range of deformation, the rolling induces a domain structure as a consequence of a nonhomogeneous distribution of the deformation. At lower local deformation the initial morphology is still present, while at higher deformation clumps of folded chains oriented along the rolling directions are observable. The transport properties indicate that the rolling treatment reduc…

Materials scienceMorphology (linguistics)Polymers and PlasticsScanning electron microscopeMineralogyYoung's modulusGeneral ChemistryPolyethyleneDeformation (meteorology)Condensed Matter Physicslaw.inventionLow-density polyethylenesymbols.namesakechemistry.chemical_compoundchemistrylawMaterials ChemistrysymbolsElectron microscopeComposite materialFOIL methodJournal of Macromolecular Science, Part B
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Physical behavior and morphology of biaxially rolled low-density polyethyleneX

1989

Abstract Biaxial rolling was carried out on low-density polyethylene, and the rolled samples were studied using various techniques. Scanning electron microscopy and analysis of transport properties were used to obtain structural information, which was correlated to thermomechanical and dynamic-mechanical behavior. Results indicate that the initial morphology is destroyed by rolling and that clumps of molecules, like fibrils, are generated parallel to the rolling plane. The molecular orientation in the plane is mainly radial, with some reinforcement, particularly at high rolling degree, along axes diagonal with respect to the rolling directions. The rolling drastically reduces the molecular …

Materials scienceMorphology (linguistics)Polymers and PlasticsScanning electron microscopePlane (geometry)MineralogyYoung's modulusGeneral ChemistryPolyethylenePhysics::Classical PhysicsCondensed Matter PhysicsViscoelasticityAmorphous solidPhysics::Fluid Dynamicschemistry.chemical_compoundsymbols.namesakechemistryMaterials ChemistrysymbolsThermomechanical analysisComposite materialJournal of Macromolecular Science, Part B
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Incorporation of Mn12single molecule magnets into mesoporous silica

2003

The incorporation of four Mn12 derivatives, namely [Mn12O12(O2CR)16(H2O)4] (R = CH3 (1), CH3CH2 (2), C6H5 (3), C6F5 (4)), into the hexagonal channels of the MCM-41 mesoporous silica has been studied. Only the smallest clusters 1 and 2, i.e. those with compatible size with the pores of MCM-41, could enter into the mesoporous silica. Powder X-ray diffraction analysis, HRTEM images and N2 adsorption–desorption isotherm experiments show that the well-ordered hexagonal structure of MCM-41 is preserved and that the Mn12 clusters are inside the pores. The magnetic properties of the MCM-41/2b nanocomposite material obtained in CH2Cl2 indicate that the structure of the cluster is maintained after in…

Materials scienceNanocompositeMineralogyNanoparticleGeneral ChemistryMesoporous silicalaw.inventionMesoporous organosilicachemistry.chemical_compoundchemistryChemical engineeringlawMaterials ChemistryCalcinationCarboxylateMesoporous materialHigh-resolution transmission electron microscopyJ. Mater. Chem.
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