Search results for "Colloid"

showing 10 items of 1288 documents

Study of the growth of ZnS nanoparticles in water/AOT/n-heptane microemulsions by UV-absorption spectroscopy

1999

Abstract ZnS nanoparticles were synthesized at 25°C using water-containing AOT reversed micelles as nanoreactors and characterized by UV–vis spectroscopy. The time dependence of the spectra emphasizes a slow growing process of the ZnS nanoparticles coupled with a change of their photophysical properties. Both processes are well described by power laws. The nanoparticle size can be controlled by the molar ratio R ( R =[water]/[AOT]), i.e. by the micellar size. The deposits obtained by evaporation of the volatile components of the microemulsions are found to be composed of a surfactant matrix containing ZnS nanoparticles smaller and more stable than that in the corresponding microemulsions.

HeptaneMaterials scienceAnalytical chemistryNanoparticleNanoreactorEvaporation (deposition)Micellechemistry.chemical_compoundColloid and Surface ChemistryChemical engineeringchemistryPulmonary surfactantMicroemulsionSpectroscopyColloids and Surfaces A: Physicochemical and Engineering Aspects
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Synthesis and characterization of CdS nanoparticles embedded in a polymethylmethacrylate matrix

2005

CdS nanopowder capped with sodium bis(2-ethylhexyl)sulfosuccinate was synthesized by using water-in-oil microemulsions. The CdS nanoparticles of about 5 nm obtained were embedded in polymethylmethacrylate matrix by a photocuring process. The transparent yellow solid compound was characterized by optical absorption and emission spectroscopy, high-resolution transmission electron microscopy, and energy-dispersive X-ray spectroscopy. The properties of this compound were compared with those of the nanopowder dispersed in heptane and in methylmethacrylate. The results obtained indicate that the nanoparticles are homogeneously dispersed in the matrix and do not change in size during the embedding…

HeptaneMaterials sciencePhotoluminescencenanoparticleAnalytical chemistryNanoparticlemicroemulsionCdSSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryChemical engineeringchemistryTransmission electron microscopyphotoluminescenceMicroemulsionAbsorption (chemistry)LuminescenceSpectroscopymicrowave irradiationSettore CHIM/02 - Chimica Fisica
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The oxamate route, a versatile post-functionalization for metal incorporation in MIL-101(Cr): Catalytic applications of Cu, Pd, and Au

2013

Abstract A new consecutive post-functionalization method has been developed for the inclusion of additional metal functionalities in Metal Organic Frameworks (MOFs) through oxamate as chelating agent. This may result in catalytic centers of metal–organic complexes or in controlled formation of metal nanoparticles, demonstrated for Cu, Pd and Au, in the highly stable MIL-101(Cr) framework. In a first post-synthesis step, reduction of the NO 2 -MIL-101(Cr) leads to the formation of NH 2 -MIL-101(Cr). The second functionalization consists of a straightforward condensation of the amino groups of the ligand with ethyl chloro-oxoacetate resulting in the formation of free oxamates attached to the …

Heterogeneous catalysisChemistryInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisCopperPost-functionalizationCatalysisCoupling reactionCatalysisMetalMetal complexMetal organic frameworkColloidal goldNH2-MIL-101(Cr)visual_artvisual_art.visual_art_mediumNanoparticlesMetal-organic frameworkOxamateGoldPhysical and Theoretical ChemistryPalladiumCopperPalladium
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The glass transition in polymer-micronetwork colloids

1995

Dynamic light scattering experiments on a new, wore complex colloidal system reveal that the density fluctuations at high concentration follow a similar pattern as observed for molecular liquids an...

High concentrationchemistry.chemical_classificationMaterials scienceApplied MathematicsGeneral Physics and AstronomyTransportationStatistical and Nonlinear PhysicsPolymerCondensed Matter::Soft Condensed MatterColloidchemistryDynamic light scatteringChemical physicsStatistical physicsGlass transitionMathematical PhysicsTransport Theory and Statistical Physics
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Osmotic conditions in rheologic properties of erytrocites

2001

Abstract The decreasing viability and in vivo survival of red blood cells, RBCs, observed in blood bank-storage are due to alterations in their rheologic properties and metabolic status. However, there is a lack of electrokinetic experiments with erythrocytes by the screening produced by the high concentration of buffer required to keep the isoosmotic conditions. Electrokinetic measurements in a wide range of sodium chloride and tetrasodium pyrophosphate are undertaken on liposomes as cell models, and in order to get an aqueous media suitable for maintaining osmotic conditions and allowing electrophoretic mobility measurements as well, advantage has been taken of dextrose properties. Measur…

High concentrationchemistry.chemical_compoundElectrophoresisLiposomeElectrokinetic phenomenaColloid and Surface ChemistryChromatographychemistryAqueous mediumSodiumchemistry.chemical_elementTetrasodium pyrophosphateColloids and Surfaces A: Physicochemical and Engineering Aspects
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Measuring (biological) materials mechanics with atomic force microscopy. 2. Influence of the loading rate and applied force (colloidal particles)

2020

Atomic force microscopy (AFM) is the most often used tool to study the mechanical properties of eukaryotic cells. Due to their complex assembly, cells show viscoelastic properties. When performing experiments, one has to consider the influence of both loading rate and maximum load on the measured mechanical properties. Here, we employed colloidal particles of various sizes (from 2 to 20 μm diameter) to perform force spectroscopy measurements on endothelial cells at loading rates varying from 0.1 to 50 μm/s, and maximum loads ranging from 1 to 25 nN. We were able to determine the non-linear dependence of cell viscoelastic properties on the loading rate which followed a weak power law. In add…

HistologyMaterials scienceWork (physics)Force spectroscopyEndothelial CellsYoung's modulus030206 dentistry02 engineering and technologyMechanicsMicroscopy Atomic Force021001 nanoscience & nanotechnologyPower lawViscoelasticityStiffening03 medical and health sciencesMedical Laboratory Technologysymbols.namesake0302 clinical medicineColloidal particlesymbolsLoading rateAnatomy0210 nano-technologyInstrumentationMechanical PhenomenaMicroscopy Research and Technique
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Magnetic properties of colloidal cobalt nanoclusters

2010

Abstract. Co nanoclusters were synthesized by an inverse-micelle chemical route. The magnetic and microstructural properties of the nanoparticles have been analyzed as a function of the surfactant (AOT and DEHP) and the drying method. Microstructural analysis has been performed by TEM and XANES; magnetic properties have been studied by hysteresis loops and zero-field cooling - field cooling (ZFC-FC) curves. TEM images show 2 to 4 nm sized particles spherical in shape. XANES measurements point out a significant presence of Co3O4 with metallic Co and some Co2+ bound to the surfactant. The presence of antiferromagnetic Co3O4 explains the magnetic transition observed at low T in both ZFC-FC mea…

HistoryMaterials scienceAnalytical chemistrychemistry.chemical_elementNanoparticleNanotechnologyXANESComputer Science ApplicationsEducationNanoclustersMetalColloidHysteresisCondensed Matter::Materials Sciencechemistrycobalt nanoparticlesvisual_artvisual_art.visual_art_mediumAntiferromagnetismCobaltSettore CHIM/02 - Chimica Fisica
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Combinatorial Identification of Hydrides in a Ligated Ag40 Nanocluster with Noncompact Metal Core

2019

No formation of bulk silver hydride has been reported. Until very recently, only a few silver nanoclusters containing hydrides have been successfully prepared. However, due to the lack of effective techniques and also poor stability of hydride-containing Ag nanoclusters, the identification of hydrides' location within Ag nanoclusters is challenging and not yet achieved, although some successes have been reported on clusters of several Ag atoms. In this work, we report a detailed structural and spectroscopic characterization of the [Ag40(DMBT)24(PPh3)8H12]2+ (Ag40H12) cluster (DMBT = 2,4-dimethylbenzenethiol). The metal framework consists of three concentric shells of Ag8@Ag24@Ag8, which can…

HydrideChemistryGeneral ChemistryElectron010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCharacterization (materials science)NanomaterialsNanoclustersNMR spectra databaseMetalCrystallographyColloid and Surface Chemistryvisual_artvisual_art.visual_art_mediumCluster (physics)Journal of the American Chemical Society
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Structural Versatility of Anion−π Interactions in Halide Salts with Pentafluorophenyl Substituted Cations

2008

A series of pentafluorophenyl substituted ammonium, iminium, amidinium, and phosphonium halides are presented which show extensive anion-pi interactions. Hereby, the well-known anion-donor-pi-acceptor as well as "eta6" anion-pi-complex type interactions are observed. The latter is supported by fixation of the anion on top of the aromatic system through hydrogen bonding. This arrangement was investigated by theoretical methods showing a highly attractive anion-pi interaction. In addition an eta2-type coordination of the anions to only two C-atoms of the electron-deficient ring system is described.

Hydrogen bondHalideIminiumGeneral ChemistryRing (chemistry)PhotochemistryBiochemistryCatalysisIonchemistry.chemical_compoundColloid and Surface ChemistrychemistryPolymer chemistryTheoretical methodsAmmoniumPhosphoniumJournal of the American Chemical Society
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Selective Formation of S4- and T-Symmetric Supramolecular Tetrahedral Cages and Helicates in Polar Media Assembled via Cooperative Action of Coordina…

2020

We report on the synthesis and self-assembly study of novel supramolecular monomers encompassing quadruple hydrogen-bonding motifs and metal-coordinating 2,2'-bipyridine units. When mixed with metal ions such as Fe2+ or Zn2+, the tetrahedron cage complexes are formed in quantitative yields and full diastereoselectivity, even in highly polar acetonitrile or methanol solvents. The symmetry of the complexes obtained has been shown to depend critically on the flexibility of the ligand. Restriction of the rotation of the hydrogen-bonding unit with respect to the metal-coordinating site results in a T-symmetric cage, whereas introducing flexibility either through a methylene linker or rotating be…

Hydrogen bondLigandMetal ions in aqueous solutionSupramolecular chemistryGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographyBipyridineColloid and Surface ChemistrychemistryMethyleneAcetonitrileJournal of the American Chemical Society
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