Search results for " surface"

showing 10 items of 2838 documents

Characterization of Rabbit Mesenchymal Cell Attachment on Calcium Phosphate Surface

2014

In the current study, the effect of three different treated surfaces of hydroxyapatite and β-tricalcium phosphate on mesenchymal cell attachment has been investigated. Calcium phosphate powders have been synthesized, uniaxially pressed, polished and sintered. Mesenchymal cells have been seeded onto unpolished, polished and polished-thermally etched ceramic samples. The ceramic samples have been characterized by XRD, FTIR and SEM. Results have shown that the best cell attachment and morphology are on the unpolished surface indicating that relatively rough surface is better for cell application.

implant surfaceMaterials scienceMorphology (linguistics)mesenchymal cellsMesenchymal stem celltechnology industry and agriculturechemistry.chemical_elementRabbit (nuclear engineering)CalciumPhosphateβ-tricalcium phosphatehumanitieseye diseasesHydroxyapatitechemistry.chemical_compoundchemistryChemical engineeringvisual_artRough surfaceHydroxyapatite implant surface mesenchymal cells β-tricalcium phosphatevisual_art.visual_art_mediumCeramicFourier transform infrared spectroscopyBiomedical engineering
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Surface treatments for titanium implants

2015

The implant surface is considered one of the most important factors for osteointegration. A factor that proved to be crucial for a better, faster osteointegration is surface roughness. It has been widely shown that an increase in roughness corresponds to a better microretention between implant and bone macromolecules. Titanium surface can be prepared with different techniques in order to obtain an optimal degree of surface roughness, an increase of TiO2 thickness, or even to create a coating of osteoconductive material. This article describes the most widely used and investigated techniques to modify a titanium implant surface: Addition techniques: titanium oxide layer thickening, TPS (Tita…

implant surfacedental implantSettore MED/28 - Malattie Odontostomatologicheosteointegration
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Self-Assembled Molecular Rafts at Liquid|Liquid Interfaces for Four-Electron Oxygen Reduction

2011

The self-assembly of the oppositely charged water-soluble porphyrins, cobalt tetramethylpyridinium porphyrin (CoTMPyP(4+)) and cobalt tetrasulphonatophenyl porphyrin (CoTPPS(4-)), at the interface with an organic solvent to form molecular "rafts", provides an excellent catalyst to perform the interfacial four-electron reduction of oxygen by lipophilic electron donors such as tetrathiafulvalene (TTF). The catalytic activity and selectivity of the self-assembled catalyst toward the four-electron pathway was found to be as good as that of the Pacman type cofacial cobalt porphyrins. The assembly has been characterized by UV-visible spectroscopy, Surface Second Harmonic Generation, and Scanning …

inorganic chemicals2Nd-Harmonic Generationchemistry.chemical_elementPhotochemistryBiochemistryOxygenCatalysisCatalysischemistry.chemical_compoundWater-Soluble PorphyrinsColloid and Surface ChemistryCobalt Porphyrinsheterocyclic compoundsLiquid/Liquid Interface2Nd DerivativesEnergyDioxygenPolarizable Continuum ModelGeneral ChemistryPorphyrinRadical CationchemistryRadical ionSurface second harmonic generationDensity functional theoryImmiscible Electrolyte-SolutionsCobaltTetrathiafulvalene
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Substituent Effects on the [N-I-N](+) Halogen Bond

2016

We have investigated the influence of electron density on the three-center [N-I-N](+) halogen bond. A series of [bis(pyri din e) io dine](+) and [1,2-bis ( (pyridin e-2-71 ethynyl)b e nze n e)io dine](+) BF4- complexes substituted with electron withdrawing and donating functionalities in the para-position of their pyridine nitrogen were synthesized and studied by spectroscopic and computational methods. The systematic change of electron density of the pyridine nitrogens upon alteration of the para-substituent (NO2, CF3, H, F, Me, OMe, NMe2) was confirmed by N-15 NMR and by computation of the natural atomic population and the pi electron population of the nitrogen atoms. Formation of the [N-…

inorganic chemicalsElectron densityPopulationInorganic chemistryhalogen bondsSubstituent010402 general chemistry01 natural sciencesBiochemistryCatalysisArticlechemistry.chemical_compoundColloid and Surface ChemistryPyridineeducationBenzeneta116education.field_of_studyHalogen bond010405 organic chemistryChemical shiftGeneral ChemistryKemi0104 chemical sciencesCrystallographychemistryChemical SciencesPolar effect
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The enrichment ratio of atomic contacts in crystals, an indicator derived from the Hirshfeld surface analysis

2014

An enrichment ratio is derived from the decomposition of the crystal contact surface between pairs of interacting chemical species. The propensity of different contact types to form is investigated.

inorganic chemicalsHydrogeneducationStackingchemistry.chemical_element010402 general chemistrybehavioral disciplines and activities01 natural sciencesBiochemistryCrystal[CHIM.CRIS]Chemical Sciences/CristallographyHirshfeld surface analysisGeneral Materials ScienceChemical compositionhealth care economics and organizationsCrystallography010405 organic chemistryChemistryHydrogen bondIntermolecular forceGeneral ChemistryCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter PhysicsResearch Papersfingerprint plotshumanities0104 chemical sciencesCrystallographyChemical speciesQD901-999Fluorineenrichment ratiocrystal packingIUCrJ
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Optical determination and identification of organic shells around nanoparticles: application to silver nanoparticles

2013

We present a simple method to prove the presence of an organic shell around silver nanoparticles. This method is based on the comparison between optical extinction measurements of isolated nanoparticles and Mie calculations predicting the expected wavelength of the Localized Surface Plasmon Resonance of the nanoparticles with and without the presence of an organic layer. This method was applied to silver nanoparticles which seemed to be well protected from oxidation. Further experimental characterization via Surface Enhanced Raman Spectroscopy (SERS) measurements allowed to identify this protective shell as ethylene glycol. Combining LSPR and SERS measurements could thus give proof of both …

inorganic chemicalsMaterials scienceMie scatteringeducationSilver nanoparticleShell (structure)FOS: Physical sciencesNanoparticlePhysics::Optics02 engineering and technology010402 general chemistry01 natural sciencesSilver nanoparticlesurface enhanced raman spectroscopychemistry.chemical_compoundlocalized surface plasmon resonanceMesoscale and Nanoscale Physics (cond-mat.mes-hall)Physics::Atomic and Molecular ClustersMie theoryGeneral Materials ScienceSurface plasmon resonancehealth care economics and organizationsPlasmonCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale Physicstechnology industry and agricultureMaterials Science (cond-mat.mtrl-sci)Surface-enhanced Raman spectroscopy021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical scienceschemistryChemical engineering[SPI.OPTI]Engineering Sciences [physics]/Optics / Photonicorganic shells0210 nano-technologyEthylene glycol
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Highly Active Co3O4-Based Catalysts for Total Oxidation of Light C1–C3 Alkanes Prepared by a Simple Soft Chemistry Method: Effect of the Heat-T…

2021

9 figures, 2 tables.

inorganic chemicalsTechnologyInorganic chemistryTotal oxidationcobalt oxidechemistry.chemical_elementalkane oxidationpropaneHeterogeneous catalysissurface oxygen vacanciesMethaneArticleCatalysischemistry.chemical_compoundPropaneAlkane oxidationSurface oxygen vacanciesPropanetotal oxidationvolatile organic compoundsGeneral Materials ScienceReactivity (chemistry)Volatile organic compoundsCobalt oxideAlkanechemistry.chemical_classificationHeterogeneous catalysisEthaneMicroscopyQC120-168.85methaneTQH201-278.5ethaneEngineering (General). Civil engineering (General)TK1-9971heterogeneous catalysischemistryDescriptive and experimental mechanicsMixed oxideElectrical engineering. Electronics. Nuclear engineeringTA1-2040cobalt oxide; total oxidation; alkane oxidation; heterogeneous catalysis; volatile organic compounds; propane; ethane; methane; surface oxygen vacanciesCobaltMethaneMaterials; Volume 14; Issue 23; Pages: 7120
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CO2 Fixation by Copper(II) Complexes of a Terpyridinophane Aza Receptor

2004

CO2 is fixed by a Cu2+ complex of a macrocyclic terpyridinophane ligand forming a carbamate group. Several features of the structure mimic the enzyme rubisco.

inorganic chemicalschemistry.chemical_classificationCarbamateReaction mechanismbiologyChemistryStereochemistrymedicine.medical_treatmentfungiCarbon fixationRuBisCOfood and beverageschemistry.chemical_elementmacromolecular substancesGeneral ChemistryLigand (biochemistry)BiochemistryCopperCatalysisColloid and Surface ChemistryEnzymemedicinebiology.proteinReceptorJournal of the American Chemical Society
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Soluble/MOF-Supported Palladium Single Atoms Catalyze the Ligand-, Additive-, and Solvent-Free Aerobic Oxidation of Benzyl Alcohols to Benzoic Acids.

2021

Metal single-atom catalysts (SACs) promise great rewards in terms of metal atom efficiency. However, the requirement of particular conditions and supports for their synthesis, together with the need of solvents and additives for catalytic implementation, often precludes their use under industrially viable conditions. Here, we show that palladium single atoms are spontaneously formed after dissolving tiny amounts of palladium salts in neat benzyl alcohols, to catalyze their direct aerobic oxidation to benzoic acids without ligands, additives, or solvents. With this result in hand, the gram-scale preparation and stabilization of Pd SACs within the functional channels of a novel methyl-cystein…

inorganic chemicalschemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysisMetalColloid and Surface ChemistryAtom economyMetal·lúrgiaDissolutionSolvent freeChemistryLigandQuímicaGeneral ChemistryCombinatorial chemistry0104 chemical sciencesSoluble/MOFOrganic reactionAlcoholsvisual_artvisual_art.visual_art_mediumPalladiumJournal of the American Chemical Society
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From Single Molecules to Nanoscopically Structured Materials: Self-Assembly of Metal Chalcogenide/Metal Oxide Nanostructures Based on the Degree of P…

2011

A chemically specific and facile method for the immobilization of metal oxide nanoparticles onto the surface of IF-MoS2 nested fullerenes is reported. The modification strategy is based on the chalcophilic affinity of transition metals such as Fe2+/Fe3+, Fe3+, or Zn2+ as described by the Pearson HSAB concept. The binding capabilities of the 3d metals are dictated by their Pearson hardness. Pearson hard cations such as Fe3+ (Fe2O3) do not bind to the chalcogenide surfaces; borderline metals such as Fe2+ (Fe3O4) or Zn2+ (ZnO) bind reversibly. Pearson-soft metals like Au bind irreversibly. The immobilization of metal oxide nanoparticle colloids was monitored by transmission electron microscopy…

inorganic chemicalslayered compound; metal chalcogenide; metal oxide; nanoparticle; reversible surface functionalizationMaterials scienceChalcogenidenanoparticleGeneral Chemical EngineeringInorganic chemistrylayered compoundOxideNanoparticleGeneral Chemistrymetal oxideMetalchemistry.chemical_compoundTransition metalchemistryTransmission electron microscopyvisual_artreversible surface functionalizationMaterials Chemistryvisual_art.visual_art_mediumHSAB theoryHigh-resolution transmission electron microscopymetal chalcogenideChemistry of Materials
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