Search results for "Colloid"

showing 10 items of 1288 documents

Target Analogue Imprinted Polymers with Affinity for Folic Acid and Related Compounds

2001

Two approaches to synthesize molecularly imprinted polymers with affinity for folic acid and other substituted pteridines have been compared. In the first approach, the folic acid analogue methotrexate was used as template and functional monomers capable of generating selective binding sites were searched in a miniaturized screening system based on binding assessment in the batch mode. Highest selectivity was seen using 2-vinylpyridine as functional monomer, which was confirmed in the chromatographic mode for a batch synthesized on a gram scale. However, the retentivity and selectivity of this phase were insufficient for anticipated applications. In a second approach, using methacrylic acid…

chemistry.chemical_classificationbiologyPolymersPteridinesMolecularly imprinted polymerGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundFolic AcidMethotrexateColloid and Surface ChemistryEnzymeMethacrylic acidchemistryDihydrofolate reductasemedicinebiology.proteinOrganic chemistryBinding siteSelectivityPteridinemedicine.drugJournal of the American Chemical Society
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Single Particle Motion of Hard-Sphere-Like Polymer Micronetwork Colloids Up to the Colloid Glass Transition

1997

Polymer micronetwork spheres swollen in a good solvent can be regarded as colloids which require no special stabilisation to avoid aggregation. Their interactions can be timed by changing the degree of internal crosslinking. The phase behaviour and the static structure factor demonstrate that crosslink density of 1:10 (inverse number of monomer units between crosslinks) is sufficient to achieve hard sphere behaviour. We designed a host-tracer system consisting of core-shell micronetwork spheres (core: polystyrene; shell: poly-t-butylacrylate) in a host of refractive-indexmatched poly-t-butylacrylate micronetwork colloids. Employing a crosslink density of 1:10 and tuning the polydispersity s…

chemistry.chemical_classificationchemistry.chemical_compoundColloidMaterials sciencechemistryDynamic light scatteringChemical physicsPhase (matter)DispersityPolymerPolystyreneGlass transitionStructure factor
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Reversible, room-temperature C—C bond activation of benzene by an isolable metal complex

2019

The activation of C-C bonds is of fundamental interest in the construction of complex molecules from petrochemical feedstocks. In the case of the archetypal aromatic hydrocarbon benzene, C-C cleavage is thermodynamically disfavored, and is brought about only by transient highly reactive species generated in situ. Here we show that the oxidative addition of the C-C bond in benzene by an isolated metal complex is not only possible, but occurs at room temperature and reversibly at a single aluminium center in [(NON)Al]- (where NON = 4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimethylxanthene). Selectivity over C-H bond activation is achieved kinetically and allows for the generation…

chemistry.chemical_classificationchemistry.chemical_elementGeneral Chemistry010402 general chemistryCleavage (embryo)Photochemistry01 natural sciencesBiochemistryOxidative additionCatalysis3. Good health0104 chemical sciencesMetalchemistry.chemical_compoundColloid and Surface ChemistrychemistryAluminiumvisual_artvisual_art.visual_art_mediumMoleculeBenzeneSelectivityAromatic hydrocarbon
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Stratification in Drying Polymer–Polymer and Colloid–Polymer Mixtures

2017

Drying polymer-polymer and colloid-polymer mixtures were studied using Langevin dynamics computer simulations. Polymer-polymer mixtures vertically stratified into layers, with the shorter polymers enriched near the drying interface and the longer polymers pushed down toward the substrate. Colloid-polymer mixtures stratified into a polymer-on-top structure when the polymer radius of gyration was comparable to or smaller than the colloid diameter, and a colloid-on-top structure otherwise. We also developed a theoretical model for the drying mixtures based on dynamical density functional theory, which gave excellent quantitative agreement with the simulations for the polymer-polymer mixtures a…

chemistry.chemical_classificationendocrine systemdigestive oral and skin physiologyStratification (water)Thermodynamics02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicscomplex mixtures01 natural sciences0104 chemical sciencesbody regionsColloidchemistryElectrochemistryRadius of gyrationOrganic chemistryGeneral Materials ScienceDensity functional theory0210 nano-technologyLangevin dynamicsSpectroscopyLangmuir
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Phospholipid-based reverse micelles.

1990

Physicochemical investigations on the aggregation of phospholipids (mainly phosphatidylcholines) in organic solvents are reviewed and compared with the aggregation behaviour of phospholipids in aqueous medium. In particular we review the data showing that phosphatidylcholines (lecithins) form reverse micellar structures in certain apolar solvents. In these systems not only low molecular weight compounds but also catalytically active enzymes and entire cells can be solubilized. In addition, highly viscous phosphatidylcholine gels can be obtained in organic solvents upon solubilizing a critical amount of water. Generally, phospholipid-based reverse micelles can be regarded as thermodynamicall…

chemistry.chemical_classificationfood.ingredientChemical PhenomenaOrganic Chemistrytechnology industry and agriculturePhospholipidBiological membraneCell BiologyBiochemistryMicelleLecithinColloidchemistry.chemical_compoundChemistryEnzymefoodchemistryPhosphatidylcholineOrganic chemistrylipids (amino acids peptides and proteins)MicroemulsionColloidsMolecular BiologyMicellesPhospholipidsChemistry and physics of lipids
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Structural Investigation of Water/Lecithin/Cyclohexane Microemulsions by FT-IR Spectroscopy

1995

Abstract FT-IR spectra of water/lecithin/deuterated cyclohexane microemulsions as a function of water/lecithin molar ratio R ( R = [water]/[lecithin]) at various volume fractions ( O ) of the micellar phase have been recorded at 25°C. After elimination of the small spectral contributions due to deuterated cyclohexane and normalization, the shape of the C–H stretching band due to lecithin has been found dependent upon R and O whereas that of the O–H stretching band has been found dependent only upon R . The change in shape of the C–H band was interpreted in terms of a modification of the lecithin alkyl chain packing order. The analysis of the O–H band provides evidence that the hydroxylic gr…

chemistry.chemical_classificationfood.ingredientCyclohexaneHydrogen bondChemistryLecithinSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryfoodDeuteriumPhase (matter)Organic chemistryPhysical chemistryMicroemulsionAlkylJournal of Colloid and Interface Science
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Structural characterization of U(VI) surface complexes on kaolinite in the presence of humic acid using EXAFS spectroscopy.

2007

To determine the influence of humic acid (HA), pH, and presence of atmospheric CO2 on the sorption of U(VI) onto kaolinite, the structure of the surface complexes was studied by U L III-edge extended X-ray absorption fine structure (EXAFS) spectroscopy. The best fits to the experimental EXAFS data were obtained by including two uranium coordination shells with two axial (O ax) and five equatorial (O eq) oxygen atoms at 1.77+/-0.02 and 2.34+/-0.02 A, respectively, and two coordination shells with one Al/Si atom each at 3.1 and 3.3 A. As in the case of the binary system U(VI)-kaolinite, uranium forms inner-sphere surface complexes by edge sharing with aluminum octahedra and/or silicon tetrahe…

chemistry.chemical_classificationsorptionkaoliniteExtended X-ray absorption fine structureAnalytical chemistrySorptionhumic acidSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsEXAFSColloid and Surface ChemistryAdsorptionchemistryX-ray photoelectron spectroscopyuranium(VI)XPSHumic acidKaoliniteAbsorption (chemistry)surface complexesSpectroscopyJournal of colloid and interface science
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Absolutes Molekulargewicht der nativen Cellulose der Alge Valonia

1976

Der Polymerisationsgrad der nativen Cellulose der Alge Valonia wurde bei dem unfraktionierten Material zu Pw≈26500 und bei dem durch Fallungsfraktionierung isolierten hochmolekularen Anteil der Molekulargewichtsverteilung zu Pw≈44000 ermittelt. Diese letzte Grose legt die Dimension fest, die die synthetisierende Matrize geometrisch erfullen mus. Sie durfte um einen Faktor von ca. 3 groser sein als die bei der Baumwollcellulose mit Pw≈14000. In Verbindung mit anderen Untersuchungen wird eine Biosynthese des Cellulosemolekuls als sehr wahrscheinlich angesehen, die direkt auf einer flachenformigen Matrize zu einer gefalteten Kette fuhrt. Da die thermodynamisch kontrollierte Faltungslange zu me…

chemistry.chemical_compoundChain structureColloid and Surface ChemistrybiologyPolymers and PlasticsPolymer scienceChemistryPolymer chemistryMaterials ChemistryCelluloseValoniaPhysical and Theoretical Chemistrybiology.organism_classificationColloid and Polymer Science
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Synthesis, Structure, and Reactivity of the First Enantiomerically Pure Ortho-Metalated Rhodium(II) Dimer

1999

chemistry.chemical_compoundColloid and Surface ChemistryChemistryStereochemistryDimerchemistry.chemical_elementReactivity (chemistry)General ChemistryBiochemistryMedicinal chemistryCatalysisRhodiumJournal of the American Chemical Society
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Immobilisation of humic substances

2002

Attempts were made to immobilise humic substances (HS) by grafting them onto different carriers (styrene-divinylbenzene copolymers, cellulose and silica) as well as by their crosslinking with formaldehyde. Reaction with Merrifield resin was used for the immobilisation of HS, coupling by means of water-soluble carbodiimides to carriers containing amino-groups. Crosslinking of HS with formaldehyde (also in presence of other substances able to enter polycondensation reactions with formaldehyde) was shown to be an efficient method for their insolubilisation. Properties of the obtained immobilised HS were studied, including their potential use as sorbents for several metal ions and organic subst…

chemistry.chemical_compoundColloid and Surface ChemistryCondensation polymerAdsorptionChemistryMetal ions in aqueous solutionInorganic chemistryFormaldehydeCopolymerOrganic chemistryCelluloseGraftingMerrifield resinColloids and Surfaces A: Physicochemical and Engineering Aspects
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