Search results for "Material chemistry"

showing 10 items of 413 documents

Synthesis and fluorescence emission of neutral and anionic di- and tetra-carboranyl compounds

2011

A new family of photoluminescent neutral and anionic di-carboranyl and tetra-carboranyl derivatives have been synthesized and characterized. The reaction of α,α'-bis(3,5-bis(bromomethyl)phenoxy-m-xylene with 4 equiv. of the monolithium salt of 1-Ph-1,2-C(2)B(10)H(11) or 1-Me-1,2-C(2)B(10)H(11) gives the neutral tetracarboranyl-functionalized aryl ether derivatives closo-1 and closo-2, respectively. The addition of the monolithium salt of 1-Ph-1,2-closo-C(2)B(10)H(11) to α,α,'-dibromo-m-xylene or 2,6-dibromomethyl-pyridine gives the corresponding di-carboranyl derivatives closo-3 and closo-4. These compounds, which contain four or two closo clusters, were degraded using the classical method,…

Boron CompoundsModels MolecularMagnetic Resonance SpectroscopySubstituentSalt (chemistry)Ether010402 general chemistryPhotochemistryCrystallography X-Ray01 natural sciencesInorganic Chemistrychemistry.chemical_compoundPolymer chemistryPyridineMoleculeta116Tetramethylammoniumchemistry.chemical_classificationLuminescent Agents010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryAryl[CHIM.MATE]Chemical Sciences/Material chemistry0104 chemical sciencesSpectrometry FluorescencechemistryCarborane
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Reversible switching of the electronic ground state in a pentacoordinated Cu(ii) complex.

2013

International audience; An easy reversible switching of the electronic ground state in a pentacoordinated copper(ii) complex is reported for the first time. The simple protonation of a carboxylic group in a Cu(ii) complex with a {dx(2)-y(2)}(1) electronic configuration leads to a flip of the ground electronic configuration from {dx(2)-y(2)}(1) to {dz(2)}(1) in the metal ion.

Carboxylic groupMolecular Conformationchemistry.chemical_elementInorganic compoundsElectronsProtonationCrystallography X-Ray010402 general chemistry01 natural sciencesCatalysisMetalCoordination ComplexesComputational chemistryElectronic ground stateMaterials Chemistry010405 organic chemistryChemistryMetals and AlloysGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryCopper3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsReversible switchingvisual_artCeramics and Compositesvisual_art.visual_art_mediumQuantum TheoryPhysical chemistryElectron configurationGround stateCopper
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Exceptional affinity of nanostructured organic-inorganic hybrid materials towards dioxygen: confinement effect of copper complexes

2007

We report the exceptional reactivity towards dioxygen of a nanostructured organic-inorganic hybrid material due to the confinement of copper cyclam within a silica matrix. The key step is the metalation reaction of the ligand, which can occur before or after xerogel formation through the sol-gel process. The incorporation of a Cu(II) center into the material after xerogel formation leads to a bridged Cu(I)/Cu(II) mixed-valence dinuclear species. This complex exhibits a very high affinity towards dioxygen, attributable to auto-organization of the active species in the solid. The remarkable properties of these copper complexes in the silica matrix demonstrate a high cooperative effect for O(2…

Cations DivalentMetalationInorganic chemistrychemistry.chemical_elementLigands010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundAdsorptionHeterocyclic CompoundsCyclamPolymer chemistryOrganometallic CompoundsLamellar structureReactivity (chemistry)ComputingMilieux_MISCELLANEOUSdioxygen bindingBinding Sites010405 organic chemistryLigandsol-gel processesSpectrum AnalysisOrganic ChemistryTemperatureGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistrySilicon DioxideCopperEnzymesNanostructuresPeroxides0104 chemical sciencesOxygenchemistrytetraazamacrocyclesMultiprotein Complexescopper[ CHIM.MATE ] Chemical Sciences/Material chemistryAnisotropyAdsorptionHybrid materialGelsorganic-inorganic hybrid composites
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Thermal sprayed coatings for protection against cavitation erosion

2018

In order to protect the hydraulic components from cavitation erosion phenomena, the parts are often coated by thermal spraying. Buck YSZ shows an excellent performance against cavitation erosion. However, the cavitation erosion resistance of YSZ coatings have vaguely been studied. Therefore, in this study, YSZ were manufactured with different thermal spraying processes and post-treated by laser remelting, then they were subjected to cavitation tests according to ASTM G32.The YSZ coating was first manufactured by atmospheric plasma spraying (APS). Various sizes of YSZ powder and different preheating temperatures of the substrate were studied to observe their effect on the cavitation behavior…

Cavitation[CHIM.MATE] Chemical Sciences/Material chemistryYszPlasma spravingNumerical modelling[CHIM.MATE]Chemical Sciences/Material chemistryModélisation numériqueNiCrBSiCaviationProjection plasma sous videRefusion laserLaser remelting
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On the Interaction between 1D Materials and Living Cells

2020

One-dimensional (1D) materials allow for cutting-edge applications in biology, such as single-cell bioelectronics investigations, stimulation of the cellular membrane or the cytosol, cellular capture, tissue regeneration, antibacterial action, traction force investigation, and cellular lysis among others. The extraordinary development of this research field in the last ten years has been promoted by the possibility to engineer new classes of biointerfaces that integrate 1D materials as tools to trigger reconfigurable stimuli/probes at the sub-cellular resolution, mimicking the in vivo protein fibres organization of the extracellular matrix. After a brief overview of the theoretical models r…

Cellular membraneMaterials sciencelcsh:BiotechnologyBiomedical EngineeringTheoretical modelsregenerative medicineNanotechnologyBiointerface02 engineering and technologyReviewbioelectronics010402 general chemistry01 natural sciencesRegenerative medicineBiomaterials1D materialsbiointerfacelcsh:TP248.13-248.651D materials CNTs bioelectronics biointerface photocatalysis polymers regenerative medicineMicroscale chemistrypolymerslcsh:R5-920BioelectronicsCNTs021001 nanoscience & nanotechnology0104 chemical sciencesProtein fibreslcsh:Medicine (General)0210 nano-technologyphotocatalysisMaterial chemistryJournal of Functional Biomaterials
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Investigation of magnesium phosphate cement hydration in diluted suspension and its retardation by boric acid

2016

Abstract Magnesium phosphate cements (MPCs) are used for rapid repair works, but they may also offer prospects for the stabilization/solidification of deleterious waste. MPCs contain calcined magnesium oxide and a water-soluble acid phosphate, such as potassium dihydrogen phosphate (KH 2 PO 4 ). The main precipitated hydrate is then K-struvite (MgKPO 4 ·6H 2 O). This work aims at giving new insight into the processes involved in its formation. Since cement hydration is very rapid, the second objective is to understand how boric acid, a common admixture for field application, retards cement hydration. A multi-stage process is evidenced in diluted suspension: MgHPO 4 ·7H 2 O likely precipitat…

CementMagnesium phosphateMaterials scienceMagnesiumPotassiumInorganic chemistry0211 other engineering and technologieschemistry.chemical_element02 engineering and technologyBuilding and Construction[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPhosphateBoric acidchemistry.chemical_compoundchemistry021105 building & construction[CHIM]Chemical SciencesGeneral Materials Science0210 nano-technologyHydrateDissolutionComputingMilieux_MISCELLANEOUS
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Changes in Cement Paste and Mortar Fluidity after mixing induced by PCP: A parametric study

2006

International audience; The interaction mechanism between polycarboxylate-type superplasticizer (PCP) and cement hydration is not fully understood and incompatibilities between concrete and additive are sometimes observed. In some cases, the fluidity tends to increase (“overfluidification”) few minutes after mixing. This is a problem because the overfluidification leds to bleeding of the concrete which could be critical on job site. Our study consisted first in highlighting the phenomenon of “over-fluidification” by slump flow tests on mortar. Next, the time evolution of the rheological behaviour of cement pastes in the presence of PCP was analysed thanks to a rheometry protocol in order to…

Cement[CHIM.MATE] Chemical Sciences/Material chemistryMaterials scienceslump flowRheometrySuperplasticizerMixing (process engineering)[CHIM.MATE]Chemical Sciences/Material chemistryfluidityCivil engineeringsulphatePCPAdsorption“over-fluidification”Rheologyadsorption[ CHIM.MATE ] Chemical Sciences/Material chemistryComposite materialMortarParametric statistics
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Hydration of tricalcium aluminate in the presence of various amounts of calcium sulphite hemihydrate : Conductivity tests.

2006

Abstract Hydration of calcium aluminate C3A (3CaO·Al2O3) in the presence of calcium sulphite hemihydrate (CaSO3·0.5H2O), with the molar ratio of substrates close to 1, produces the C3A·CaSO3·11H2O calcium monosulphite aluminate phase. Small amounts of calcium sulphite added to calcium aluminate (the ratio of CaSO3·0.5H2O / C3A equalling 0 : 1) change the rate of C3A hydration and influence the whole reaction. Reaction processes for various ratios of the C3A–CaSO3·0.5H2O mixture were examined in pure distilled water with a considerable amount of liquid W / S = 38–50 (constant W / C3A). Processes in the liquid phase were monitored with conductivity equipment, and the XRD analysis was used to …

Cementtricalcium aluminateAluminateInorganic chemistrychemistry.chemical_elementBuilding and Constructioncalcium sulphite hemihydrateConductivityCalciumchemistry.chemical_compoundDistilled waterchemistryPhase (matter)[ CHIM.MATE ] Chemical Sciences/Material chemistryX-ray crystallographyhydration productsGeneral Materials ScienceTricalcium aluminatehydration
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Enhanced quantum sieving of hydrogen isotopes via molecular rearrangement of the adsorbed phase in chabazite

2020

Coadsorption experiments reveal an unexpected increase of the D2/H2 selectivity with loading in pure silica chabazite at 47 K. This effect is correlated with the appearance of a step in the adsorption isotherms of H2 and D2. Grand canonical Monte Carlo simulations show that this phenomenon is related to a molecular rearrangement of the adsorbed phase induced by its strong confinement. In the case of a H2 and D2 mixture, this rearrangement favors the adsorption of D2 having a smaller size due to quantum effects.

ChabaziteHydrogenchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysisAdsorptionPhase (matter)Materials ChemistryMolecular rearrangementQuantumComputingMilieux_MISCELLANEOUSIsotopeMetals and AlloysGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryChemical physicsCeramics and Composites0210 nano-technologySelectivity
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Average versus local structure in K2NiF4-type LaSrAlO4: direct experimental evidence of local cationic ordering

2012

The long-range ordering of a crystalline material can be accurately determined by analyzing the Bragg intensities and positions. In contrast, direct observation of short-range ordering in crystalline materials, which is increasingly considered of fundamental importance to unravel the structure-property relationships that underpin their technological applications, is a challenging task. In this study we have investigated the structure of LaSrAlO4, a representative example of compounds with the K2NiF4-type structure. By the combined use of synchrotron and neutron diffraction, pair distribution function analysis, Al-27 MQMAS NMR and atomistic simulations we have highlighted differences between…

ChemistryNeutron diffractionCationic polymerizationStructure (category theory)Pair distribution function02 engineering and technologyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryType (model theory)010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesLocal structureSynchrotron0104 chemical scienceslaw.inventionCrystallographylawChemical physicsK2NiF4 neutron diffraction 27Al MAS NMR quadrupolar interaction local structureMaterials ChemistryRange (statistics)Local structure NMR0210 nano-technologyComputingMilieux_MISCELLANEOUS
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