Search results for "Colloid"

showing 10 items of 1288 documents

Spectroscopic and structural characterization of pure and FeCl3-containing tri-n-butyl phosphate

2014

The spectroscopic properties and liquid structure of pure tri-n-butyl phosphate (TBP) and FeCl3/TBP solutions have been investigated by Uv–Vis and Raman spectroscopies, X-ray diffraction and conductometry. Uv–Vis and Raman spectra, supported by conductometric measurements, consistently indicate that the solubilized salt is present mostly as TBP n [FeCl3 − n ] n+ and FeCl4 − complex ions due to specific interaction with the TBP phosphate group. Thanks to this interaction, a high amount of salt (up to 13 % w/w) can be dissolved despite the relatively low dielectric constant of TBP. The X-ray diffractogram of pure TBP has been interpreted in terms of three main contributions which can be attri…

chemistry.chemical_classificationPolymers and PlasticsConductometryChemistryInorganic chemistryTri-N-butyl PhosphateFeCl3 . Tri-n-butyl phosphate . Self-assembling . Local structures .Amphiphilic solventsNanoparticleSalt (chemistry)Ionic bondingTri-n-butyl phosphatePhosphatesymbols.namesakechemistry.chemical_compoundColloid and Surface ChemistryFeCl3Materials ChemistrysymbolsMoleculeSelf-assemblingAmphiphilic solventsPhysical and Theoretical ChemistryLocal structuresRaman spectroscopy
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Microstructure and lateral diffusion in monolayers of polymerizable amphiphiles

1989

Lipid analogue amphiphilic molecules containing polymerizable units were investigated in monolayers at the air/water interface by using film balance measurements, fluorescence microscopy, and photobleaching techniques. The polymerizable groups (diene-, diyne-, and methacrylate units) were introduced into the hydrophobic alkyl chains or into the polar head of the amphiphilic molecules. In the case of the diene- and diyne-containing compounds the polymerizable units are incorporated into the hydrophobic alkyl chains, enabling them to form a two-dimensional network. Due to the free chain flexibility of the monomers the lateral mobility was comparable to that of saturated lipid analogues and de…

chemistry.chemical_classificationPolymers and PlasticsDiacetylenePolymerMethacrylatechemistry.chemical_compoundColloid and Surface ChemistryMonomerPhotopolymerchemistryPolymerizationMonolayerPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryAlkylColloid & Polymer Science
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Hydrogen bonds in unpolar matrix — Comparison of complexation in polymeric and low molecular-weight systems

1991

By ene-reaction of 4-phenyl-1,2,4-triazoline-3,5-dione with double bonds, polar 4-phenyl-1,2,4-triazolidine-3,5-dione (phenyl urazole) groups are introduced into unpolar matrices. Hydrogen-bond complexes are formed between two amide-like units. The temperature dependence of complex formation in dilute hydrocarbon medium is obtained from remperature-dependent IR spectra in the region of the C=O stretching vibration. Results obtained for a low molecular-weight model system are compared with modified polybutadienes, where the groups are attached statistically along the polymer backbone. The enthalpy and the entropy of complex formation (ΔH f =−28.6 kJ/mol; ΔS f =−52 J/mol K−1) obtained for the…

chemistry.chemical_classificationPolymers and PlasticsDouble bondChemistryStereochemistryHydrogen bondEnthalpyInfrared spectroscopyPolymerStandard enthalpy of formationCrystallographyColloid and Surface ChemistryHydrocarbonMaterials ChemistryPhysical and Theoretical ChemistryEquilibrium constantColloid and Polymer Science
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Hetero-Telechelic Dye-Labeled Polymer for Nanoparticle Decoration

2009

The synthesis of poly(methyl methacrylate) (PMMA) exhibiting one fluorescent dye (Texas Red) and one methyl disulfide end group is described. It is shown that the latter end group enabled the exchange of both oleic amine on gold nanoparticles (AuNP) and of oleic acid on CdSe/ZnS quantum dots (QD), allowing for a phase transfer of both types of nanoparticles (NP) from hexane into dimethylformamide due to the solubility provided by the PMMA chains. For AuNP, a fluorescence quenching of the dye was found due to fluorescence resonance energy transfer (FRET) from the dye to the AuNP, while QDs caused a fluorescence enhancement by FRET from the QD to the attached dyes. Due to the hetero-telecheli…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryNanoparticleTexas RedPolymerFluorescencechemistry.chemical_compoundEnd-groupFörster resonance energy transferchemistryColloidal goldPolymer chemistryMaterials ChemistryMethyl methacrylateMacromolecular Rapid Communications
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Computer simulation of macromolecular materials

1988

Computer simulation of model systems with Monte Carlo methods enables the detailed study of structure and thermodynamic properties of these systems and thus constitutes a link between analytic theory and experiment. Typical applications that are discussed include polymer blends, dynamics of local motions in polymer melts, and the adsorption of polymers on walls.

chemistry.chemical_classificationPolymers and PlasticsPolymer scienceMonte Carlo methodPolymerCondensed Matter::Soft Condensed MatterReptationMolten stateColloid and Surface ChemistrychemistryMaterials ChemistryPolymer blendStatistical physicsPhysical and Theoretical ChemistryDiffusion (business)Phase diagramMacromoleculeColloid & Polymer Science
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Synthesis and characterization of water-swellable?,?-polyasparthydrazide derivatives

1995

α, β-polyasparthydrazide (PAHy) was crosslinked by glutaraldehyde to form water-swellable materials possessing a three-dimensional molecular network. Different crosslinking degrees were prepared varying glutaraldehyde/PAHy ratio and samples containing 5-fluorouracil were obtained by incorporating the drug into the polymer networks during the crosslinking reaction. All samples were characterized by swelling tests, thermal, x-ray and SEM analysis. Their microstructure was observed through scanning electron microscopy. Furthermore, for samples containing the anticancer drug,in vitro release studies were performed in pH 7.4 buffer solution.

chemistry.chemical_classificationPolymers and PlasticsScanning electron microscopetechnology industry and agriculturemacromolecular substancesPolymerBuffer solutionMicrostructureIn vitrochemistry.chemical_compoundColloid and Surface ChemistrychemistrySelf-healing hydrogelsMaterials ChemistrymedicineGlutaraldehydePhysical and Theoretical ChemistrySwellingmedicine.symptomNuclear chemistryColloid & Polymer Science
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Structural variations in amphiphiles: Discoidal multivalent cations

1986

Fourteen cationic multipolar amphiphiles have been synthesized with pyridinium or trimethylammonium head groups. The hydrophobic cores are planar ring systems (benzene or triphenylene) to which two, three, four, or six decylene or undecylene alkyl chains are attached by ester linkages. The hydrophilic head groups are bound to the outer ends of the alkyl chains.

chemistry.chemical_classificationPolymers and PlasticsStereochemistryChemistryCationic polymerizationTriphenyleneRing (chemistry)Micellechemistry.chemical_compoundColloid and Surface ChemistryLiquid crystalPolymer chemistryAmphiphileMaterials Chemistrylipids (amino acids peptides and proteins)PyridiniumPhysical and Theoretical ChemistryAlkylColloid & Polymer Science
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Unexpectedly normal phase behavior of single homopolymer chains

2006

Employing Monte Carlo simulations, we show that the topology of the phase diagram of a single flexible homopolymer chain changes in dependence on the range of an attractive square well interaction between the monomers. For a range of attraction larger than a critical value, the equilibrium phase diagram of the single polymer chain and the corresponding polymer solution phase diagram exhibit vapor (swollen coil, dilute solution), liquid (collapsed globule, dense solution), and solid phases. Otherwise, the liquid-vapor transition vanishes from the equilibrium phase diagram for both the single chain and the polymer solution. This change in topology of the phase diagram resembles the behavior k…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodEnthalpyThermodynamicsPolymerConformational entropyCritical valueCondensed Matter::Soft Condensed MatterColloidchemistryEntropy (order and disorder)Phase diagramPhysical Review E
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Development of core-shell colloids to study self-diffusion in highly concentrated dispersions

2007

To study single particle motion in highly concentrated colloidal dispersions, a host-tracer colloid system was developed, consisting of crosslinked polymer micronetwork spheres placed in a good solvent. The host colloid is made invisible to the experimental probe by matching its refractive index to that of the solvent. For the tracer particles a core-shell structure was chosen to ensure the interaction potential to be identical to that of the host particles. Therefore the shell was made of the same polymer as the host. The core differs in refractive index from the solvent and is therefore visible due to scattered light.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesSelf-diffusionMaterials scienceShell (structure)PolymerCondensed Matter::Soft Condensed MatterCore (optical fiber)ColloidchemistryDynamic light scatteringChemical physicsSPHERESRefractive index
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A thermodynamic analysis on the coincidence of extrema conditions in the sorption equilibrium for ternary polymer systems

1993

Flory-Huggins theory of polymer solutions has been used to express the condition of extrema values in the total sorption, as well as the inversion point in the preferential adsorption parameters for termary polymer systems. Two approaches have been followed, the first considers the binary and ternary interaction parameters independent of polymer concentration and solvent composition. In the second one, this dependence has been introduced. Our attention is focused on the volume fraction of solvent mixture dependence of the above parameters, in order to confirm or not the coincidence between the extrema values and the inversion point. Several cosolvent and cononsolvent ternary polymer systems…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesTernary numeral systemPolymers and PlasticsChemistryThermodynamicsSorptionPolymerCoincidenceCondensed Matter::Soft Condensed MatterMaxima and minimaColloid and Surface ChemistryVolume fractionMaterials ChemistryPhysical and Theoretical ChemistrySolvent effectsTernary operationColloid & Polymer Science
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