Search results for "nanoparticle"

showing 10 items of 2198 documents

Controlling the cohesion of cement paste

2005

The main source of cohesion in cement paste is the nanoparticles of calcium silicate hydrate (C-S-H), which are formed upon the dissolution of the original tricalcium silicate (C(3)S). The interaction between highly charged C-S-H particles in the presence of divalent calcium counterions is strongly attractive because of ion-ion correlations and a negligible entropic repulsion. Traditional double-layer theory based on the Poisson-Boltzmann equation becomes qualitatively incorrect in these systems. Monte Carlo (MC) simulations in the framework of the primitive model of electrolyte solution is then an alternative, where ion-ion correlations are properly included. In addition to divalent calciu…

Inorganic chemistryIonic bonding02 engineering and technologyElectrolyteCement pasteCSH010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundlawElectrochemistryGeneral Materials Sciencecalcium silicate hydrateCalcium silicate hydrateDissolutionionic correlationsSpectroscopyion-ion correlations[CHIM.MATE] Chemical Sciences/Material chemistrySurfaces and Interfaces[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPotassium sulfateSilicate0104 chemical sciencesC-S-HPortland cementchemistryChemical engineering[ CHIM.MATE ] Chemical Sciences/Material chemistryCalcium silicatenanoparticles0210 nano-technologycement cohesioncharge reversal
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Easy Route to Functionalize Iron Oxide Nanoparticles via Long-Term Stable Thiol Groups

2009

International audience; The functionalization of superparamagnetic iron oxide nanoparticles (SPIOs) by meso-2,3-dimercaptosuccinic acid (DMSA) was investigated. Under ambient conditions, the thiol groups from DMSA are not stable and do not allow a direct functionalization without storage in stringent conditions or a chemical regeneration of free thiols. In this study, we have developed a protocol based on poly(ethylene glycol) (PEG) grafting of SPIO prior to DMSA anchoring. We have observed that PEG helps to increase the stability of thiol groups under ambient conditions. The thiol functionalized SPIOs were stable under physiological pH and ionic strength as determined by Ellman's essay and…

Inorganic chemistryIron oxide02 engineering and technology010402 general chemistryFerric Compounds01 natural scienceschemistry.chemical_compoundPEG ratioElectrochemistryReactive dyeGeneral Materials ScienceSulfhydryl CompoundsSpectroscopychemistry.chemical_classificationMolecular Structure[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry[CHIM.MATE]Chemical Sciences/Material chemistrySurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter PhysicsCombinatorial chemistry0104 chemical sciencesModels ChemicalchemistryIonic strength[ CHIM.MATE ] Chemical Sciences/Material chemistryThiolNanoparticlesSurface modificationSuccimer0210 nano-technologyEthylene glycolIron oxide nanoparticlesLangmuir
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Versatile wet-chemical synthesis of non-agglomerated CaCO3 vaterite nanoparticles.

2011

Calcium carbonate (vaterite) nanoparticles of 20-60 nm size were obtained without stabilizing tensides by heating a dispersion of calcium bicarbonate (CaHCO(3)) in ethylene glycol for 30 minutes at 40 to 100 °C.

Inorganic chemistryMetals and AlloysNanoparticleGeneral ChemistryChemical synthesisCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCalcium carbonatechemistryCalcium bicarbonateVateriteMaterials ChemistryCeramics and CompositesDispersion (chemistry)Ethylene glycolChemical communications (Cambridge, England)
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Au deposited on CeO2 prepared by a nanocasting route: A high activity catalyst for CO oxidation

2014

Abstract A set of catalysts comprised of gold on different CeO 2 supports has been prepared by a nanocasting route and characterized by several physicochemical techniques. These catalysts have been tested for CO oxidation and show outstanding catalytic activity. Higher calcination temperatures of the hard template, producing a poorly ordered silica template, have led to a higher amount of oxygen vacancies on the surface of CeO 2 . The presence of surface oxygen defects in the support combined with the deposition of Au nanoparticles ( ca. 3 nm) homogeneously dispersed on the CeO 2 support may explain the excellent behaviour for low temperature CO oxidation. Surprisingly, it has been observed…

Inorganic chemistryNanoparticleCatalytic combustionCatalysisCatalysislaw.inventionchemistry.chemical_compoundchemistryColloidal goldlawOxidation stateCalcinationPhysical and Theoretical ChemistryDispersion (chemistry)Carbon monoxideJournal of Catalysis
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Interaction of Alkaline Metal Cations with Oxidic Surfaces: Effect on the Morphology of SnO2 Nanoparticles

2010

Reaction pathways to SnO(2) nanomaterials through the hydrolysis of hydrated tin tetrachloride precursors were investigated. The products were prepared solvothermally starting from hydrated tin tetrachloride and various (e.g., alkali) hydroxides. The influence of the precursor base on the final morphology of the nanomaterials was studied. X-ray powder diffraction (XRD) data indicated the formation of rutile-type SnO(2). Transmission electron microscopy (TEM) studies revealed different morphologies that were formed with different precursor base cations. Data from molecular dynamics (MD) simulations provide theoretical evidence that the adsorption of the cations of the precursor base to the f…

Inorganic chemistryNanoparticlechemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsTin oxideNanomaterialsAdsorptionchemistryTransmission electron microscopyTetrachlorideElectrochemistryGeneral Materials ScienceTinSpectroscopyPowder diffraction
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Self-Immolative Linkers as Caps for the Design of Gated Silica Mesoporous Supports

2016

A new hybrid material based on sulforhodamine-B dye-loaded silica mesoporous nanoparticles capped with a self-immolative gate has been synthesized and characterized. The gated material's controlled release behavior is monitored under different pH conditions. Under acidic and neutral conditions, a low level of dye release is detected. However, at slightly basic pH, significant dye release occurs owing to deprotonation of the phenol moiety in the capping molecule, which results in its disassembly.

Inorganic chemistryNanoparticlemesoporous materials010402 general chemistry01 natural sciencesCatalysisDeprotonationmolecular devicesQUIMICA ORGANICAPolymer chemistryQUIMICA ANALITICAMoietyMolecule010405 organic chemistryChemistryOrganic ChemistryQUIMICA INORGANICApH-responsive systemsGeneral ChemistryControlled release0104 chemical sciencesMesoporous organosilicasilicadyes/pigmentsHybrid materialMesoporous material
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Physicochemical Characterization of Isomorphously Substituted FeZSM-5 during Activation

2002

Physicochemical characteristics of isomorphously substituted FeZSM-5 both after preparation and after activation have been determined by gas (Ar and N2) physisorption, 27Al and 29Si magic-angle spinning–nuclear magnetic resonance, NH3 temperature-programmed desorption, transmission electron microscopy, H2 temperature-programmed reduction (TPR), 57Fe Mossbauer spectroscopy, and voltammetric response techniques. The activation of as-synthesized FeZSM-5 comprises calcination at 823 K and a subsequent steam treatment (300 mbar of H2O in N2) at 873 K. Calcination leads to complete removal of the template. During this process a significant fraction of iron is dislodged to extraframework positions…

Inorganic chemistryOxideHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundchemistrylawDesorptionMössbauer spectroscopyCalcinationPhysical and Theoretical ChemistryZeoliteIron oxide nanoparticlesJournal of Catalysis
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Polypyrrole–palladium nanoparticles composite as efficient catalyst for Suzuki–Miyaura coupling

2012

International audience; Synthesis of a new hybrid material (Pd/PPy) composed of polypyrrole globules with uniformly incorporated Pd nanoparticles via direct redox reaction between pyrrole and Pd(NH3)(4)Cl-2 in water has been recently reported (V.A. Zinovyeva, M.A.Vorotyntsev, I. Bezverkhyy, D. Chaumont, J.-C. Hierso, Adv. Funct. Mater. 21 (2011) 1064-1075). In the actual study, this procedure has been extended to synthesize a series of Pd/PPy powders with variable palladium content and morphological parameters. Depending on the monomer-to-oxidant ratio in reaction mixture, average diameters of Pd and PPy particles may change in the ranges of 1.25-1.45 and 27-62 nm, respectively, the Pd conc…

Inorganic chemistryPVP-PD NANOPARTICLESchemistry.chemical_elementNanoparticle010402 general chemistryHeterogeneous catalysisPolypyrrole01 natural sciencesCatalysisCatalysischemistry.chemical_compoundHETEROGENEOUS PALLADIUMWATERHIGHLY-ACTIVE CATALYSTAQUEOUS-MEDIAHYDROGENATIONPhysical and Theoretical ChemistryHECKNanocomposite010405 organic chemistryProcess Chemistry and TechnologyPOLYMER0104 chemical sciencesRECYCLABLE CATALYSTchemistryReagentHybrid materialLIGAND-FREEPalladiumJournal of Molecular Catalysis A: Chemical
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Tetraurea calix[4]arenes with sulfur functions: synthesis, dimerization to capsules, and self-assembly on gold.

2007

Various calix[4]arene derivatives, fixed in the cone conformation by decylether groups and functionalized at their wide rim by urea residues, were synthesized. In two compounds (4f,g) sulfur functions were attached to the urea groups via different spacers in order to allow binding to metal surfaces. While they exist as single molecules in polar solvents, tetraurea calix[4]arenes of this type (4) combine to form dimeric capsules in aprotic, apolar solvents. A solvent molecule is usually included in such a capsule, if no guest with a higher affinity is present. In the presence of an equimolar amount of the tetratosylurea 5, the exclusive formation of heterodimers, consisting of one molecule o…

Inorganic chemistrySupramolecular chemistryBiochemistryMass SpectrometryMetalchemistry.chemical_compoundElectrolytesPhenolsCationsPolymer chemistryElectrochemistryMoleculeUreaFerrous CompoundsPhysical and Theoretical ChemistryDichloromethaneMethylene ChlorideChloroformOrganic ChemistrySurface Plasmon ResonanceSolutionschemistryModels ChemicalSolubilityvisual_artProton NMRvisual_art.visual_art_mediumSolventsNanoparticlesSelf-assemblyChloroformGoldCyclic voltammetryCalixarenesDimerizationSulfurOrganicbiomolecular chemistry
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Hemin-coupled iron(III)-hydroxide nanoparticles show increased uptake in Caco-2 cells

2011

Abstract Objectives The absorption of commonly used ferrous iron salts from intestinal segments at neutral to slightly alkaline pH is low, mainly because soluble ferrous iron is easily oxidized to poorly soluble ferric iron and ferrous iron but not ferric iron is carried by the divalent metal transporter DMT-1. Moreover, ferrous iron frequently causes gastrointestinal side effects. In iron(III)-hydroxide nanoparticles hundreds of ferric iron atoms are safely packed in nanoscaled cores surrounded by a solubilising carbohydrate shell, yet bioavailability from such particles is insufficient when compared with ferrous salts. To increase their intestinal uptake iron(III)-hydroxide nanoparticles …

Inorganic chemistryTetrazolium SaltsPharmaceutical ScienceNanoparticleFerrozineIron Chelating AgentsFerric CompoundsFerrouschemistry.chemical_compoundMicroscopy Electron TransmissionSpectroscopy Fourier Transform InfraredmedicineHumansScattering RadiationParticle SizeColoring AgentsHemePharmacologyChemistryIron Chelating AgentsIron deficiencymedicine.diseaseCulture MediaThiazolesHeminNanoparticlesHydroxideColorimetrySpectrophotometry UltravioletProtoporphyrinCaco-2 CellsHeminJournal of Pharmacy and Pharmacology
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