Search results for "Ceramic"

showing 10 items of 2129 documents

The effect of partial exfoliation of multilayer silicate filler particles on the elastic properties of a polymer composite

2018

Abstract A method for stepwise calculation the elastic constants of a three-phase composite, including the polymer matrix, the fully exfoliated silicate nanolayers and the platelike silicate particles in the form of multilayer intercalated stacks is considered. A theoretical analysis is carried out by using the Mori–Tanaka theory of an equivalent medium. The influence of degree of exfoliation (the ratio of exfoliated filler content to the total filler content) on the reinforcing efficiency is studied and discussed. A comparative analysis of experimental data of elastic modulus for a rigid polyurethane/montmorillonite composite and prediction results is carried out. It is shown, that with gr…

chemistry.chemical_classificationFiller (packaging)Materials scienceComposite number02 engineering and technologyPolymer021001 nanoscience & nanotechnologyExfoliation jointSilicatechemistry.chemical_compound020303 mechanical engineering & transportsMontmorillonite0203 mechanical engineeringchemistryCeramics and CompositesComposite material0210 nano-technologyElastic modulusCivil and Structural EngineeringPolyurethaneComposite Structures
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Mechanical behaviour of Mater-Bi/wood flour composites: a statistical approach

2008

Interest in biocomposites (lignocellulosic filled biopolymers) started in the 90s, due to environmental advantages, related to the full biodegradability of both matrix and filler, economical issues (organic fillers usually come from sawmill or agriculture wastes) and aesthetical issues (wood filled biopolymers could be particularly pleasant if used for indoor furnishing and automotive interior). In this work, a method for a systematic study of the properties of Mater-Bi®/wood flour composites is presented. A two-level full factorial model was built. It allows investigating the effects of multiple operative variables on the observed properties, their contributions, their optimal combinations…

chemistry.chemical_classificationFiller (packaging)Materials sciencestatistical properties/methodelectron microscopyMixing (process engineering)polymer-matrix composites (PMCs)Izod impact strength testWood flourPolymerAspect ratio (image)Settore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryMechanics of MaterialsCeramics and CompositesHeat deflection temperaturemechanical propertieComposite materialElastic modulus
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Diferrocenyl tosyl hydrazone with an ultrastrong NHFe hydrogen bond as double click switch.

2014

The intramolecular NH⋯Fe hydrogen bond in diferrocenyl hydrazone 2 raises the barrier for intramolecular electron transfer in its mixed-valent cation 2+ and is only disrupted by double oxidation to 22+.

chemistry.chemical_classificationHydrogen bondMetals and AlloysHydrazoneGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferchemistryTosylIntramolecular forceMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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Maghemite polymer nanocomposites with modulated magnetic properties

2007

A method is presented for the production of maghemite polymer nanocomposites with modulated magnetic properties. Magnetic nanocomposites prepared using this method show regular variation in the magnetic blocking temperature from 2 K to 300 K, and variation in the saturation magnetization from 0 to 50 emu g � 1 (Fe2O3). The method is based on the in situ formation of maghemite nanoparticles in nitrogen-base polymer matrixes. The particle size can be varied regularly from 1.5 nm to 16 nm by changing the ratio of iron loading in the polymer and/or the Fe(II)/Fe(III) ratios. The particles are isolated and uniformly distributed within the matrix. The mate

chemistry.chemical_classificationIn situNanocompositeMaterials sciencePolymers and PlasticsPolymer nanocompositeMetals and AlloysMaghemiteNanoparticlePolymerengineering.materialElectronic Optical and Magnetic MaterialsNuclear magnetic resonancechemistryChemical engineeringCeramics and CompositesengineeringParticle sizeActa Materialia
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Crystal structures, infrared-spectra, and thermal behavior of calcium hydrogenselenite monohydrate, Ca(HSeO3)2 · H2O, and dicalcium diselenite bis(hy…

1986

Abstract Calcium hydrogenselenite monohydrate and dicalcium diselenite bis(hydrogenselenite) were synthesized and their crystal structures determined. Crystal data for Ca(HSeO3)2 · H2O: a = 6.911(2), b = 7.369(2), c = 6.739(2) A, α = 90.51(3)°, β = 90.93(3)°, γ = 107.46(2)°, V = 327.3(2) A3, space group P 1 (No. 2), dcalcd = 3.19 M gm−3, Z = 2, and R = 0.036 for 1503 reflections. Data for Ca2(HSeO3)2(Se2O5): a = 14.719(4), b = 7.059(2), c = 11.793(2) A, β = 117.96(2)°, V = 1082.3(4) A3, space group C2 c (No. 15), dcalcd = 3.52 Mg m−3, Z = 4, and R = 0.047 for 1251 reflections. Both structures form a three-dimensional network. The coordination polyhedron around calcium is a monocapped trigon…

chemistry.chemical_classificationInfraredInfrared spectroscopychemistry.chemical_elementCrystal structureCalciumCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystallographyTrigonal prismchemistryCrystal dataX-ray crystallographyMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryInorganic compoundJournal of Solid State Chemistry
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Synthesis, characterization and thermal properties of small R2R′2N+X−-type quaternary ammonium halides

2005

Twenty-one R {sub 2} R {sup '} {sub 2}N{sup +} X {sup -} -type (R=methyl or ethyl, R {sup '}=alkyl, X=Br or I) quaternary ammonium (QA) halides have been prepared by using a novel one-pot synthetic route in which a formamide (dimethyl-, diethylformamide, etc.) is treated with alkyl halide in the presence of sodium or potassium carbonate. The formation of QA halides was verified with {sup 1}H-NMR, {sup 13}C-NMR, MS and elemental analysis. The crystal structures of four QA halides (two bromide and two iodide) were determined using X-ray single crystal diffraction, and the powder diffraction method was used to study the structural similarities between the single crystal and microcrystalline bu…

chemistry.chemical_classificationInorganic chemistryHalideCrystal structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryIonic liquidX-ray crystallographyMaterials ChemistryCeramics and CompositesMelting pointPhysical and Theoretical ChemistrySingle crystalAlkylPowder diffractionJournal of Solid State Chemistry
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Structural evolution of Pt/ceria-zirconia TWC catalysts during the oxidation of carbon monoxide

2004

The structural evolution of two Pt/ceria–zirconia catalysts, characterized by different amounts of supported Pt, was monitored by in situ X-ray diffraction during the anaerobic oxidation of CO at different temperatures. In a first phase, oxygen coming from the surface layers of the ceria–zirconia mixed oxide is consumed and no structural variation of the support is observed. After this induction time, bulk reduction of Pt/ceria–zirconia takes place as a step-like process, while the CO2 production continues at a nearly constant rate. This behavior is totally different from that of the metal-free support in similar reaction conditions, that show a gradual bulk reduction. In repeated oxidation…

chemistry.chemical_classificationInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsChemical reactionElectronic Optical and Magnetic MaterialsCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryTransition metalMaterials ChemistryCeramics and CompositesMixed oxideCubic zirconiaCompounds of carbonPhysical and Theoretical ChemistryPlatinumCarbon monoxide
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The first structurally characterized cationic lanthanide–alkyl complexesElectronic supplementary information (ESI) available: experimental and spectr…

2002

Reaction of rare earth metal–alkyl complexes [Ln(CH2SiMe3)3(THF)2] (Ln = Y, Lu) with B(C6X5)3 (X = H, F) in the presence of crown ethers gives crystallographically characterized ion pairs [Ln(CH2SiMe3)2(CE)(THF)n]+[B(CH2SiMe3)(C6X5)3]– (CE = [12]-crown-4, n = 1; CE = [15]-crown-5 and [18]-crown-6, n = 0).

chemistry.chemical_classificationLanthanideStereochemistryRare earthMetals and AlloysCationic polymerizationGeneral ChemistryIon pairsMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryMaterials ChemistryCeramics and CompositesAlkylChemical Communications
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Voltammetric Identification of Lead(II) and (IV) in Mediaeval Glazes in Abrasion-Modified Carbon Paste and Polymer Film Electrodes. Application to th…

2000

Direct identification of lead(II) and (IV) in glazed ceramics by cyclic voltammetry and differential pulse voltammetry is described. Characteristic cathodic and anodic profiles are obtained for microsample coatings in Paraloid B72-film electrodes immersed in NaCl and HAc/NaAc media. The electrochemical response of PbO, PbO2 and Pb3O4, and a series of test specimens of glaze is compared with that of microsamples extracted from the glaze of blue and white decorated ceramic produced in Manises (Spain) in the 15th century which have been buried in a damp place. Under abrasive conditions, striping peaks at –0.12 and –0.25 V (vs. SCE) appear for Pb(IV) centers and, at –0.55 and –0.75 V, for Pb(II…

chemistry.chemical_classificationMaterials scienceAbrasion (mechanical)GlazeMetallurgyPolymerElectrochemistryAnalytical Chemistrychemistryvisual_artElectrodeElectrochemistryvisual_art.visual_art_mediumCeramicDifferential pulse voltammetryCyclic voltammetryNuclear chemistryElectroanalysis
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Surface and Intercalation Chemistry of Polycarboxylate Copolymers in Cementitious Systems.

2009

International audience; The Ca–Al-layered double hydroxide, the so-called AFm phase, is a product of cement hydration. It is shown that the interaction of this phase with anionic polycarboxylate ether (PCE)-based dispersant polymers is not a simple adsorption but a more complex intercalation phenomenon leading to the transient sequestration of the PCE within the AFm crystallites. As a result, part of the PCE is immobilized, forming a layered organo-mineral composite, and does not play its role of a dispersing agent. This article presents, along general considerations on the links between cement chemistry and rheology, a detailed investigation of the formation, structure, and stability of a …

chemistry.chemical_classificationMaterials scienceCoprecipitationIntercalation (chemistry)Composite number0211 other engineering and technologies02 engineering and technologyPolymerNeutron scattering021001 nanoscience & nanotechnologychemistry.chemical_compoundAdsorptionchemistryChemical engineeringPhase (matter)021105 building & constructionMaterials ChemistryCeramics and CompositesComposite material0210 nano-technologyAFm phase
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