Search results for "silica."

showing 10 items of 1087 documents

ChemInform Abstract: Stereoselective Synthesis of Substituted Tetrahydropyran Rings via 6-exo and 6-endo Selenoetherification.

2010

Eight unsaturated alcohols were cyclized by selenoetherification in 6-exo or 6-endo manner to give substituted tetrahydropyran rings. Yields, regio- and stereoselectivities were discussed in terms of steric and electroniceffects such as Se-O interaction. For the first time examples of the use of silica gel in selenoetherification and the effect of the X - counter ion of PhSe + on the reaction course are discussed. These effects are related to the occurrence of Se-O interaction.

Steric effectschemistry.chemical_classificationchemistry.chemical_compoundchemistrySilica gelOrganic chemistryStereoselectivityGeneral MedicineTetrahydropyranCounterionChemInform
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The Marine Sponge-Derived Inorganic Polymers, Biosilica and Polyphosphate, as Morphogenetically Active Matrices/Scaffolds for the Differentiation of …

2014

The two marine inorganic polymers, biosilica (BS), enzymatically synthesized from ortho-silicate, and polyphosphate (polyP), a likewise enzymatically synthesized polymer consisting of 10 to >100 phosphate residues linked by high-energy phosphoanhydride bonds, have previously been shown to display a morphogenetic effect on osteoblasts. In the present study, the effect of these polymers on the differential differentiation of human multipotent stromal cells (hMSC), mesenchymal stem cells, that had been encapsulated into beads of the biocompatible plant polymer alginate, was studied. The differentiation of the hMSCs in the alginate beads was directed either to the osteogenic cell lineage by …

Stromal cellAlginatesPolymersCellular differentiationOsteogenesis DistractionPharmaceutical ScienceBone Morphogenetic Protein 2biosilica; polyphosphate; multipotent stromal cells; mesenchymal stem cells; alkaline phosphatase; 3D cell/tissue printing; distraction osteogenesisBone morphogenetic protein 2ChondrocyteArticleCollagen Type IGlucuronic AcidPolyphosphatesDrug Discoverymedicinemultipotent stromal cellsAnimalsHumansbiosilicaPharmacology Toxicology and Pharmaceutics (miscellaneous)lcsh:QH301-705.5Collagen Type IImesenchymal stem cells3D cell/tissue printingOsteoblastsTissue ScaffoldsChemistryHexuronic AcidsMesenchymal stem cellBiomaterialpolyphosphateCell DifferentiationAnatomyChondrogenesisAlkaline PhosphataseSilicon DioxideCell biologyPoriferamedicine.anatomical_structuredistraction osteogenesislcsh:Biology (General)Alkaline phosphataseMarine Drugs
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Fe-periclase reactivity at Earth's lower mantle conditions: Ab-initio geochemical modelling

2017

Intrinsic and extrinsic stability of the (Mg, Fe) O solid mixture in the Fe-Mg-Si-O system at high P, T conditions relevant to the Earth's mantle is investigated by the combination of quantum mechanical calculations (Hartree-26 Fock/DFT hybrid scheme), cluster expansion techniques and statistical thermodynamics. Iron in the (Mg, Fe) O binary mixture is assumed to be either in the low spin (LS) or in the high spin (HS) state. Un-mixing at solid state is observed only for the LS condition in the 23-42 GPa pressure range, whereas HS does not give rise to un-mixing. LS (Mg, Fe) O un-mixings are shown to be able to incorporate iron by subsolidus reactions with a reservoir of a virtual bridgmanit…

Subsolidus reaction modellingMgO-FeO binary010504 meteorology & atmospheric sciencesSilicate perovskiteLower mantle geochemical heterogeneitiesAnalytical chemistryAb initioLower mantle geochemical heterogeneities MgO-FeO binary Mixing Gibbs energy Pyrolitic geochemical mode Subsolidus reaction modellingMineralogyengineering.material010502 geochemistry & geophysics01 natural sciencesMantle (geology)Geochemistry and PetrologyMixing Gibbs energy0105 earth and related environmental sciencesPyrolitic geochemical modeSettore GEO/06 - MineralogiaPyrolitic geochemical modelAmbientaleDiamondHartreePartition coefficientengineeringPericlaseMgO-FeO binaryPyrolitic geochemical modelLower mantle geochemical heterogeneitiesSubsolidus reaction modellingMixing Gibbs energyGeologyCluster expansion
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Cryopreservation of white mulberry (Morus alba L.) by encapsulation-dehydration and vitrification

2011

Shoot apices of in vitro-grown plantlets of white mulberry, Morus alba L. cv Florio, were cryopreserved using either encapsulation-dehydration or vitrification. For encapsulation-dehydration, alginate beads containing apices were dehydrated for 1, 3, 5 or 7 days in a liquid medium containing various sucrose concentrations (0.5, 0.75, 1.0 or 1.25 M). Bead desiccation was performed using silica gel for either 0, 4, 6, 8, 9 or 14 h. For vitrification, apices were directly immersed for either 5, 15, 30 or 60 min in a vitrification solution (PVS2). Following encapsulation-dehydration, treatment of alginate beads with 0.75 M sucrose was more effective in promoting re-growth of explants after imme…

SucroseSilica gelHorticultureBiologymedicine.diseaseCryopreservationAlginate beads PVS2 Re-growth Silica gel Sucrosechemistry.chemical_compoundHorticulturechemistryShootBotanymedicineVitrificationDehydrationDesiccationExplant culture
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Baeyer—Villiger Oxidation in Supercritical CO2 with Potassium Peroxomonosulfate Supported on Acidic Silica Gel.

2006

Supercritical carbon dioxide (scCO2) is an efficient reaction medium to perform the Baeyer-Villiger oxidation with hydrated silica-supported potassium peroxomonosulfate (h-SiO2.KHSO5) under flow-through conditions. Hydration modulates the reactivity of the active surface by softening the acidity of the KHSO4 present in the supported reagent. The reaction in scCO2 is much more efficient than in n-hexane under similar conditions, which is attributed to better transport and solvating properties of the supercritical medium with regard to n-hexane.

Supercritical water oxidationSupercritical carbon dioxideChemistrySilica gelOrganic ChemistryInorganic chemistryGeneral MedicinePotassium peroxymonosulfateSupercritical fluidBaeyer–Villiger oxidationchemistry.chemical_compoundReagentCarbon dioxideReactivity (chemistry)ChemInform
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Luminescence from nearly isolated surface defects in silica nanoparticles

2015

A structured emission/excitation pattern, proper of isolated defects, arises in a vacuum from silica nanoparticles. The luminescence, centered around 3.0-3.5 eV, is characterised by a vibronic progression due to the phonon coupling with two localised modes of frequency  ∼1370 cm(-1) and  ∼360 cm(-1), and decays in about 300 ns at 10 K. On increasing the temperature, the intensity and the lifetime decrease due to the activation of a non-radiative rate from the excited state. Concurrently, the temperature dependence of the lineshape evidences the low coupling with non-localised modes of the matrix (Huang-Rhys factor S ~ 0.2) and the poor influence of the inhomogeneous broadening. These findin…

Surface (mathematics)Field (physics)ChemistryPhononNanotechnologyCondensed Matter PhysicsMolecular physicsCrystallographic defectAmorphous solidExcited statetime-resolved luminescence silica nanoparticles point defects vibronic transitions electron–phonon couplingGeneral Materials ScienceLuminescenceIntensity (heat transfer)Journal of Physics: Condensed Matter
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Structural properties of core and surface of silica nanoparticles investigated by Raman spectroscopy

2013

We studied the experimental Raman spectra of various commercial silica nanoparticles of average diameter from 7 to 40 nm and specific surface from 50 to 380 m2/g. We found that the peculiarities of the particles Raman spectra systematically depend on their specific surface. In detail, the peak position of the R band at about 440 cm−1 shifts towards high wavenumbers following an almost linear dependence on the specific surface. Similarly, the amplitudes of the D1 and D2 bands, at about 495 and 605 cm−1, respectively, increase linearly with the same quantity. Our results are interpreted in the frame of the shell model for the nanoparticles clarifying that the network of the core of the nanopa…

Surface (mathematics)Materials scienceAnalytical chemistryShell (structure)NanoparticleRing (chemistry)Silica nanoparticlesCore (optical fiber)symbols.namesakesymbolsWavenumberGeneral Materials ScienceRaman spectroscopySpectroscopyJournal of Raman Spectroscopy
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Luminescence of the surface nonbridging oxygen hole center in silica: Spectral and decay properties

2008

We investigated the red luminescence in a porous film of silica nanoparticles, originating from surface nonbridging oxygen hole centers. The excitation spectrum was measured from 1.8 to 8.0 eV by a tunable laser system and a synchrotron radiation source; this spectrum evidences a peak at 2.0 eV, nearly overlapping with the emission, and an ultraviolet broadband with peaks at 4.8 and 6.0 eV. The emission is characterized by a spectrum with two subbands split by 0.07 eV, its decay occurs with lifetime longer than 30 microsec and undergoes a thermal quenching by a factor aboout 2 with increasing temperature from 10 to 290 K. The optical characteristics of surface and bulk centers are discussed…

Surface (mathematics)Materials sciencebusiness.industryTime resolved luminescenceOptoelectronicsdefects nanoparticles luminescence time resolved measurements silicaCenter (algebra and category theory)Condensed Matter PhysicsbusinessLuminescencePorous mediumElectronic Optical and Magnetic MaterialsNonbridging oxygen
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New insights into the surface functionalities and adsorption evolution of water molecules on silica gel surface: A study by second derivative near in…

2010

Accepted version of an article in the journal: Vibrational Spectroscopy. Published version available on Science Direct: http://dx.doi.org/10.1016/j.vibspec.2010.06.003 Surface functionalities and adsorption evolution of water molecules on silica gel samples were studied by second derivative near infrared spectroscopy. Four different silica gel samples with varying surface area were used in this experiment. Each of the dry samples was allowed to equilibrate with surrounding air and the near infrared spectra were accumulated at different time intervals using reflectance technique. The evolved spectra were analysed using second derivative technique to study the adsorption evolution of water mo…

Surface (mathematics)chemistry.chemical_compoundAdsorptionchemistrySilica gelInorganic chemistryNear-infrared spectroscopyInfrared spectroscopyMoleculePhysical chemistryVDP::Mathematics and natural science: 400::Chemistry: 440::Environmental chemistry natural environmental chemistry: 446SpectroscopySecond derivative
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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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