Search results for " Silicate"

showing 10 items of 126 documents

Al-27 and Si-29 Solid-State NMR Characterization of Calcium-Aluminosilicate-Hydrate

2012

International audience; Calcium silicate hydrate (C-S-H) is the main constituent of hydrated cement paste and determines its cohesive properties. Because of the environmental impact of cement industry, it is more and more common to replace a part of the clinker in cement by secondary cementitious materials (SCMs). These SCMs are generally alumina-rich and as a consequence some aluminum is incorporated into the C-S-H. This may have consequences on the cohesion and durability of the material, and it is thus of importance to know the amount and the location of Al in C-S-H and what the parameters are that control these features. The present paper reports the Si-29 and Al-27 MAS NMR analyses of …

Silicon0211 other engineering and technologiesAnalytical chemistryMineralogychemistry.chemical_element02 engineering and technologyClinker (cement)Inorganic Chemistrychemistry.chemical_compound021105 building & constructionDISORDERED SOLIDSPhysical and Theoretical ChemistryCalcium silicate hydrateNUCLEAR-MAGNETIC-RESONANCECementPORTLAND CEMENTSSPECTROSCOPYELECTRIC-FIELD GRADIENTSResonanceCalcium aluminosilicateMQ-MAS NMR021001 nanoscience & nanotechnologyTRICALCIUM-SILICATEC-S-HALchemistrySolid-state nuclear magnetic resonance0210 nano-technologyHydrateALUMINUM INCORPORATION
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First Evidence of Tris(catecholato)silicate Formation from Hydrolysis of an Alkyl Bis(catecholato)silicate

2022

The hydrolysis of 3-ammoniumpropylbis(catecholato)silicate 1, giving two different silica-based materials containing different amounts of tris(catecholato)silicate, is reported. The latter species can be formed through an attack of catechol to the silicon atom in the pentacoordinate complex, in which the silicon-carbon bond is further activated toward electrophilic proton cleavage. The Knoevenagel reaction was used as a probe in order to test the availability of functional groups on the surface of such materials.

SiliconHydrolysisSilicatesOrganic ChemistryPharmaceutical ScienceSilicon DioxideAnalytical Chemistryhybrid organic-inorganic material; hypervalent silicate; Knoevenagel reactionChemistry (miscellaneous)Drug DiscoveryKnoevenagel reactionMolecular MedicinePhysical and Theoretical Chemistryhybrid organic-inorganic materialhypervalent silicate
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Structural and dynamical properties of sodium silicate melts: An investigation by molecular dynamics computer simulation

2001

We present the results of large scale computer simulations in which we investigate the static and dynamic properties of sodium disilicate and sodium trisilicate melts. We study in detail the static properties of these systems, namely the coordination numbers, the temperature dependence of the Q^(n) species and the static structure factor, and compare them with experiments. We show that the structure is described by a partially destroyed tetrahedral SiO_4 network and the homogeneously distributed sodium atoms which are surrounded on average by 16 silicon and other sodium atoms as nearest neighbors. We compare the diffusion of the ions in the sodium silicate systems with that in pure silica a…

SiliconStatistical Mechanics (cond-mat.stat-mech)Coordination numberSodiumDiffusionInorganic chemistrychemistry.chemical_elementFOS: Physical sciencesGeologySodium silicateDisordered Systems and Neural Networks (cond-mat.dis-nn)Condensed Matter - Disordered Systems and Neural NetworksMolecular dynamicschemistry.chemical_compoundchemistryGeochemistry and PetrologyChemical physicsAtomPhysics::Atomic and Molecular ClustersStructure factorCondensed Matter - Statistical Mechanics
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The structure and stoichiometry of C-S-H

2004

Abstract This review relates to the models describing the structural evolution of calcium silicate hydrate (C-S-H) at the crystal–chemical level as a function of composition in terms of calcium to silicon ratio. The different models are compared and discussed in the light of recent spectroscopic and microscopic data. Taking into account the structure and the morphological properties of C-S-H, a surface reaction thermodynamic model has been proposed and discussed to predict and correlate the chemical and structural evolution of C-S-H with solution chemistry.

SiliconThermodynamicschemistry.chemical_elementMineralogyBuilding and Constructionlaw.inventionchemistry.chemical_compoundchemistrylawX-ray crystallographyCalcium silicateGeneral Materials ScienceCrystallizationCalcium silicate hydrateHydrateStoichiometryJenniteCement and Concrete Research
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Selenium affects biosilica formation in the demosponge Suberites domuncula

2005

Selenium is a trace element found in freshwater and the marine environment. We show that it plays a major role in spicule formation in the demosponge Suberites domuncula. If added to primmorphs, an in vitro sponge cell culture system, it stimulates the formation of siliceous spicules. Using differential display of transcripts, we demonstrate that, after a 72-h exposure of primmorphs to selenium, two genes are up-regulated; one codes for selenoprotein M and the other for a novel spicule-associated protein. The deduced protein sequence of selenoprotein M (14 kDa) shows characteristic features of metazoan selenoproteins. The spicule-associated protein (26 kDa) comprises six characteristic repe…

SpiculeBlotting WesternMolecular Sequence DataFluorescent Antibody Techniquechemistry.chemical_elementselenium; silica; silicatein; spicules; spongesBiochemistryAntibodiesSeleniumSponge spiculeDemospongeAnimalsAmino Acid SequenceSelenoproteinsMolecular Biologychemistry.chemical_classificationGlutathione PeroxidaseBase SequencebiologyGene Expression ProfilingProteinsCell BiologyAnatomySilicon Dioxidebiology.organism_classificationCathepsinsUp-RegulationAmino acidSuberites domunculaSpongeBiochemistrychemistrySelenoproteinSuberitesSeleniumFEBS Journal
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Crystalline nanorods as possible templates for the synthesis of amorphous biosilica during spicule formation in Demospongiae.

2009

In tandem: High-resolution TEM shows that during the initial stages of demosponge spicule formation, a primordial crystalline structure is formed within the axial filament. The recently developed electron diffraction tomography technique (ADT) reveals that the nanorods have a layered structure that matches smectitic phyllosilicates. These intracellular nanorods have been considered as precursors of mature spicules. High-resolution microscopy shows that, during the initial stages of demosponge spicule formation, a primordial crystalline structure is formed within the axial filament. The recently developed electron diffraction tomography technique reveals that the nanorods have a layered stru…

SpiculeMaterials scienceElectronsCrystal structureBiochemistrybioinorganic chemistryDemospongeSponge spiculeMicroscopy Electron TransmissionX-Ray DiffractionnanostructuresAnimalsMolecular BiologyNanotubesbiologyElectron crystallographysilicateinOrganic Chemistrybioinorganic chemistry; electron crystallography; nanostructures; silicatein; spiculesbiology.organism_classificationSilicon DioxidespiculesAmorphous solidPoriferaCrystallographyelectron crystallographyElectron diffractionMicroscopy Electron ScanningMolecular MedicineNanorodChembiochem : a European journal of chemical biology
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Investigation of Temperature-Induced Phase Transitions in DOPC and DPPC Phospholipid Bilayers Using Temperature-Controlled Scanning Force Microscopy

2004

Under physiological conditions, multicomponent biological membranes undergo structural changes which help define how the membrane functions. An understanding of biomembrane structure-function relations can be based on knowledge of the physical and chemical properties of pure phospholipid bilayers. Here, we have investigated phase transitions in dipalmitoylphosphatidylcholine (DPPC) and dioleoylphosphatidylcholine (DOPC) bilayers. We demonstrated the existence of several phase transitions in DPPC and DOPC mica-supported bilayers by both atomic force microscopy imaging and force measurements. Supported DPPC bilayers show a broad L(beta)-L(alpha) transition. In addition to the main transition …

Steric effectsPhase transition12-DipalmitoylphosphatidylcholineBiophysicsPhospholipid02 engineering and technologyMicroscopy Atomic Force010402 general chemistry01 natural sciencesPhase TransitionQuantitative Biology::Subcellular Processeschemistry.chemical_compoundTransition TemperaturePhospholipidsPhysics::Biological PhysicsMembranesBilayerTransition temperaturedigestive oral and skin physiologyBiological membrane021001 nanoscience & nanotechnology0104 chemical sciencesCondensed Matter::Soft Condensed MatterCrystallographyMembranechemistryChemical physicsDipalmitoylphosphatidylcholineAluminum Silicateslipids (amino acids peptides and proteins)0210 nano-technologyBiophysical Journal
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Experimental and theoretical evidence of overcharging of calcium silicate hydrate

2007

International audience; Electrokinetic measurements such as electrophoresis may show an inversion of the effective surface charge of colloidal particle called overcharging. This phenomenon has been studied by various theoretical approaches but up to now very few attempts of confrontation between theory and experiment have been conducted. In this work we report electrophoretic measurements as well as Monte Carlo simulations of the electrokinetic potential for the surface of calcium silicate hydrate (Csingle bondSsingle bondH), which is the major constituent of hydrated cement. In the simulations, the surface charge of Csingle bondSsingle bondH nanoparticles in equilibrium with the ionic solu…

Surface PropertiesAnalytical chemistry02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialsElectrokinetic phenomenachemistry.chemical_compoundColloid and Surface ChemistryZeta potentialElectrochemistrySurface chargeColloidsCalcium silicate hydrateParticle SizeMonte Carlo simulationRange (particle radiation)Physics::Biological PhysicsQuantitative Biology::BiomoleculesCalcium silicate hydrateSilicatesWaterZeta potentialCalcium Compounds021001 nanoscience & nanotechnologyElectrostatics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]ElectrophoresisKineticschemistryModels ChemicalChemical physicsSurface charge titrationOverchargingCalcium silicateNanoparticles[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyMonte Carlo Method
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Development and characterization of co-loaded curcumin/triazole-halloysite systems and evaluation of their potential anticancer activity.

2014

Abstract Positively charged halloysite nanotubes functionalized with triazolium salts (f-HNT) were employed as a carrier for curcumin molecules delivery. The synthesis of these f-HNT new materials is described. Their interaction with curcumin was evaluated by means dynamic light scattering (DLS) and UV–vis spectroscopy in comparison with pristine unmodified HNT (p-HNT). The curcumin load into HNT was estimated by thermogravimetric analysis (TGA) measurements, while the morphology was investigated by scanning electron microscopy (SEM) techniques. Release of curcumin from f-HNT, at three different pH values, by means of UV–vis spectroscopy was also studied. Furthermore, different cancer cell …

Thermogravimetric analysisCurcuminCell SurvivalScanning electron microscopeTriazolePharmaceutical ScienceAntineoplastic Agentsengineering.materialHalloysiteSettore MED/13 - EndocrinologiaDrug Incompatibilitychemistry.chemical_compoundhalloysite nanotubes triazolium salts drug carrier curcumin in vitro anticancer activityDynamic light scatteringCell Line TumorHumansTechnology PharmaceuticalOrganic chemistrySolubilityCell ProliferationSettore CHIM/02 - Chimica FisicaDrug CarriersNanotubesSettore CHIM/06 - Chimica OrganicaTriazolesDrug LiberationchemistryThermogravimetryMicroscopy Electron ScanningengineeringCurcuminClayAluminum SilicatesDrug carrierNuclear chemistry
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Pharmaceutical properties of supramolecular assembly of co-loaded cardanol/triazole-halloysite systems

2015

Halloysite nanotubes were explored as drug carrier for cardanol, which is considered as a promising natural anticancer active species. To this aim, besides the pristine nanoclay, a chemical modification of the nanocarrier was performed by attaching triazolium salts with different hydrophobicity at the outer surface of the hollow nanotubes. The interaction between cardanol and nanotubes was highlighted in solution by HPLC. This method proved the loading of the drug into the nanotubes. The solid dried complexes formed by pristine and modified halloysite with the cardanol were characterized by IR spectroscopy, thermogravimetric analysis as well as water contact angle to evidence the structure,…

Thermogravimetric analysisMaterials scienceCell SurvivalPharmaceutical ScienceAntineoplastic Agentsengineering.materialHalloysiteSupramolecular assemblyContact anglePhenolsCell Line TumorOrganic chemistryHumansHEPATOCELLULAR CARCINOMASettore CHIM/02 - Chimica FisicaCardanolHALLOYSITEDrug CarriersHepatocellular carcinoma Cardanol Drug carrier Halloysite HPLCNanotubesChemical modificationSettore CHIM/06 - Chimica OrganicaTriazolesDrug LiberationChemical engineeringengineeringMicroscopy Electron ScanningSettore BIO/14 - FarmacologiaClayAluminum SilicatesNanocarriersHPLCDrug carrierCARDANOLDRUG CARRIER
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