Search results for "polymers"

showing 10 items of 3567 documents

Bubble fractionation of enantiomers from solution using molecularly imprinted polymers as collectors.

1998

Adsorptive bubble separation methods have been used to enrich components from both heterogeneous and homogeneous solutions. These methods are particularly effective for processing large solution volumes at low cost. Previous work demonstrated that chiral, surface-active collectors could be used to enrich enantiomers from homogeneous solution in a foam fractionation process. In a significant extension of this work, the use of highly selective molecularly imprinted polymers (MIPs) and heterogeneous solutions for the bubble flotation of enantiomers was evaluated. The high selectivity and ease of recycling of the MIP make this a potentially powerful approach for process-scale separations from l…

Chiral auxiliaryChromatographyChemistryPolymersBubbleMolecularly imprinted polymerStereoisomerismFractionationAnalytical ChemistrySolutionschemistry.chemical_compoundSurface-Active AgentsAdsorptionChemical engineeringSeparation methodFoam fractionationAdsorptionEnantiomerAnalytical chemistry
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Layered composite based on halloysite and natural polymers: a carrier for the pH controlled release of drugs

2019

We have prepared new biohybrid materials based on halloysite nanotubes and natural polymers (alginate and chitosan) for the controlled and sustained release of bioactive species. A functional nanoarchitecture has been designed allowing us to generate a layered tablet with a chitosan/halloysite nanocomposite film sandwiched between two alginate layers. The assembly of the raw components and the final structure of the hybrid tablet have been highlighted by the morphological and wettability properties of the prepared materials. Since the biohybrid has been designed as a smart carrier, halloysite nanotubes have been first loaded with a model drug (sodium diclofenac). The effect of the tablet th…

ChitosanNanocompositeComposite numberAlginateNatural polymersHalloysiteCompositeGeneral ChemistryDiclofenac Sodiumengineering.materialControlled releaseHalloysiteCatalysisChitosanchemistry.chemical_compoundchemistryChemical engineeringDrug deliveryMaterials ChemistryengineeringWetting
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Synthesis and Functional Reconstitution of Light-Harvesting Complex II into Polymeric Membrane Architectures.

2015

One of most important processes in nature is the harvesting and dissipation of solar energy with the help of light-harvesting complex II (LHCII). This protein, along with its associated pigments, is the main solar-energy collector in higher plants. We aimed to generate stable, highly controllable, and sustainable polymer-based membrane systems containing LHCII-pigment complexes ready for light harvesting. LHCII was produced by cell-free protein synthesis based on wheat-germ extract, and the successful integration of LHCII and its pigments into different membrane architectures was monitored. The unidirectionality of LHCII insertion was investigated by protease digestion assays. Fluorescence …

Chlorophyll bChlorophyllChlorophyll aCell-Free SystemPolymersLipid BilayersLight-Harvesting Protein ComplexesGeneral ChemistryPhotochemistryFluorescenceCatalysisFluorescence spectroscopyFluorescenceLight-harvesting complexchemistry.chemical_compoundMembraneSpectrometry FluorescencechemistryChlorophyllBiophysicsLipid bilayerPeptide HydrolasesAngewandte Chemie (International ed. in English)
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Hierarchical Self-Organization of Perylene Bisimide–Melamine Assemblies to Fluorescent Mesoscopic Superstructures

2000

A series of three perylene tetracarboxylic acid bisimide dyes 3a-c bearing phenoxy substituents at the four bay positions of the perylene core were synthesized and their complexation behavior to complementary ditopic dialkyl melamines 8a-c was investigated. Binding constants and Gibbs binding energies for the hydrogen bonds between the imide and the complementary melamine moiety have been determined in several solvents by NMR and UV/Vis titration experiments with monotopic model compounds 5 and 9. The effects of the solvent polarity and specific solvent-solute interactions on the degree of polymerization of (3 x 8)n are discussed, and a general formula to estimate the chain length of [AA-BB…

ChlorophyllMagnetic Resonance SpectroscopyLightPolymersMolecular ConformationSupramolecular chemistryDegree of polymerizationImidesPhotochemistryFluorescenceCatalysischemistry.chemical_compoundNon-covalent interactionsPerylenechemistry.chemical_classificationMicroscopy ConfocalTriazinesHydrogen bondOrganic ChemistryOptical polarizationPolymerGeneral ChemistrySolutionsSupramolecular polymersMicroscopy ElectronchemistrySpectrophotometry UltravioletPeryleneChemistry – A European Journal
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Pullulan and dextran: uncommon composition dependent Flory-Huggins interaction parameters of their aqueous solutions.

2008

Vapor pressure measurements were performed for aqueous solutions of pullulan ( M w 280 kg/mol) and dextran ( M w 60 and 2100 kg/mol, respectively) at 25, 37.5, and 50 degrees C. The Flory-Huggins interaction parameters obtained from these measurements, plus information on dilute solutions taken from the literature, show that water is a better solvent for pullulan than for dextran. Furthermore, they evince uncommon composition dependencies, including the concurrent appearance of two extrema, a minimum at moderate polymer concentration and a maximum at high polymer concentration. To model these findings, a previously established approach, subdividing the mixing process into two clearly separa…

Chromatography GasPolymers and PlasticsVapor pressureThermodynamicsBioengineeringFlory–Huggins solution theoryBiomaterialschemistry.chemical_compoundMaterials ChemistryPressureSolubilityGlucanschemistry.chemical_classificationAqueous solutionChromatographyWaterPullulanDextransPolymerSolventMolecular WeightDextranchemistryModels ChemicalSolventsThermodynamicsBiomacromolecules
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Interaction of polyelectrolytes with oppositely charged micelles studied by fluorescence and liquid chromatography

2005

It is studied by spectrofluorimetry the association of ionized cationic micelles (cetyltrimethylammonium bromide, CTAB) with oppositely charged polyelectrolyte [sodium poly(styrenesulfonate), PSSNa]. CTAB provokes a change in the fluorescence intensity emitted by PSSNa. The investigated surfactants form micelle-like aggregates before critical micellar concentration (CMC). Two approaches (binding and partition equilibrium) are used to obtain the association constant, KA, number of CTAB molecules in a binding site, N, and apparent partition coefficient, Γ. Analysis of the parameters as a function of polymer concentration and ionic strength μ is performed. The effect of μ shows an enhancement …

ChromatographyAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryGeneral Physics and AstronomyMicellePolyelectrolytePartition coefficientchemistry.chemical_compoundBromideIonic strengthPartition equilibriumCritical micelle concentrationMaterials ChemistryEuropean Polymer Journal
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High-resolution pyrolysis–gas chromatography with a movable reaction zone

1997

Abstract A new device was constructed for pyrolysis–gas chromatography and it was laboratory tested. The device enables the thermal degradation of polymers inside a capillary pre-column and transfer of the reaction zone into a column oven. The pyrolysis procedure described protects the thermally sensitive compounds prior to pyrolysis, prevents the process of irreversible condensation of high-boiling pyrolysis products during the chromatographic process and eliminates extracolumn effects on the peak broadening.

ChromatographyCapillary actionOrganic ChemistryCondensationAnalytical chemistryGeneral MedicinePolyethyleneBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundThermal degradation of polymerschemistrylawScientific methodFlame ionization detectorGas chromatographyPyrolysisJournal of Chromatography A
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Non-porous microparticulate supports in high-performance liquid chromatography (HPLC) of biopolymers — concepts, realization and prospects

1986

ChromatographyChemistryHydrophilic interaction chromatographyOrganic ChemistryClinical BiochemistryFast protein liquid chromatographyReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyDisplacement chromatographyAnalytical ChemistryColumn chromatographyThermoresponsive polymers in chromatographyRealization (systems)Chromatographia
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Evaluation of advanced silica packings for the separation of biopolymers by high-perforamnce liquid chromatography

1987

Non-porous monodisperse 1.5-μm silicas were allowed to react with (A) and (B) N-acetylaminopropyltriethoxysilane to generate bonded phases useful in high-performance hydrophobic-interaction chromatography (HIC). Differences in the selectivity were observed between he amide and the ether phase. Peak capacities between 10 and 30 were achieved for several proteins with the amide and ether phase packed into columns of 36 × 8 mm I.D. and elution of the proteins under chromatographic conditions in which the gradient volume, VG, was held constant by varying the gradient time between 20 and 2.5 min and the flow-rate between 0.5 and 4.0 ml/min. The S values derived from the dependences of log k′ on …

ChromatographyElutionChemistryHydrophilic interaction chromatographyOrganic ChemistryDispersityAnalytical chemistryGeneral MedicineReversed-phase chromatographyBiochemistryAnalytical ChemistryCountercurrent chromatographyVolume fractionThermoresponsive polymers in chromatographyChromatography columnJournal of Chromatography A
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Molecularly imprinted polymer-based device for field collection of oral fluid samples for cocaine identification.

2020

In this paper, a low-cost, rapid, easy, and potentially portable tool for the identification of cocaine and its semi-quantitative determination in oral fluid has been proposed. A field collection device has been designed, based on a cotton pad with an indicator and a molecularly imprinted polymer (MIP) sorbent, to selective retain cocaine from oral fluid components. After sample collection, cocaine is transferred by using phosphate buffer to the MIP and then eluted with 2-propanol. The obtained extract is analysed by ion mobility spectrometry (IMS), providing a cut-off value of 20 µg L-1 that identifies 100 % true-positive and 95 % true-negative samples. The MIP-IMS procedure has been valid…

ChromatographyElutionIon-mobility spectrometryChemistryPolymers010401 analytical chemistryOrganic ChemistryMolecularly imprinted polymerGeneral Medicine010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistryMolecular ImprintingSubstance Abuse DetectionHealth personnelIdentification (information)CocaineIon Mobility SpectrometryOral fluidHumansSample collectionSalivaLateral flow immunoassayJournal of chromatography. A
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