Search results for "Surfactant"

showing 10 items of 397 documents

Quantitative retention–structure and retention–activity relationships of barbiturates by micellar liquid chromatography

1998

Abstract Studies on the structural requirements of chromatographic surfaces to emulate in vitro the partitioning process in biomembranes are of great interest. The use of micellar mobile phases in RPLC modifies the hydrophobicity of the stationary phase and provides hydrophobic and electrostatic sites of interaction as a consequence of the adsorption of surfactant monomers to the chromatographic surface. Modified stationary phases in MLC could be structurally similar to biomembranes, but thorough studies are necessary to confirm this. In this paper we focus our attention on barbiturates. The influence of the nature and concentration of the surfactant (Brij 35, SDS and CTAB) and the mobile p…

ChromatographyOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundAdsorptionMonomerPulmonary surfactantchemistryStationary phaseMicellar liquid chromatographyPhase (matter)Journal of Chromatography A
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Determination of water-soluble vitamins in energy and sport drinks by micellar electrokinetic capillary chromatography

2016

Abstract A method for the determination of water-soluble vitamins in several energy and sport drinks by micellar electrokinetic chromatography (MEKC) has been developed in this work. The separation of vitamins was studied in terms of background electrolyte composition (borate content, pH, surfactant type and content) and in other MEKC parameters. A study of the possible compounds found in the vitamin-enriched drinks that could interfere in vitamin determination was also performed, and a modified procedure with enhanced resolution was developed. The proposed method was successfully applied to the analysis of water-soluble vitamins in a variety of energy and sport drinks and also in fruit nec…

ChromatographyResolution (mass spectrometry)Chemistry010401 analytical chemistry04 agricultural and veterinary sciences040401 food science01 natural sciencesMicellar electrokinetic chromatography0104 chemical sciences0404 agricultural biotechnologyPulmonary surfactantReagentWater-Soluble VitaminSample preparationElectrolyte compositionSoft drinkFood ScienceBiotechnologyFood Control
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On the Measurement of Dead Time in Micellar Liquid Chromatography

1996

Abstract Modelling of the retention of solutes in micellar liquid chromatography allows the optimization of the resolution of a mixture of solutes and the determination of physico-chemical retention parameters. Both tasks imply the calculation of capacity factors, which are severely affected by the value of dead time. However, the determination of the dead time is not easy when a micellar mobile phase is used owing to the wide and variable perturbations that appear at the heads of the chromatograms. Four different criteria of determination of a reference time in the chromatograms are proposed and compared. The criteria are applied to mobile phases containing a varying concentration of surfa…

ChromatographyResolution (mass spectrometry)ChemistryClinical BiochemistryAnalytical chemistryPharmaceutical ScienceDead timeBiochemistryCapacity factorAnalytical ChemistryPulmonary surfactantMicellar liquid chromatographyPhase compositionPhase (matter)Retention timeJournal of Liquid Chromatography & Related Technologies
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Role of the co-surfactant nature in soybean w/o microemulsions.

2008

Abstract The influence of the co-surfactant on physicochemical properties of w/o soybean oil microemulsions (MEs) has been studied. In spite of the similarity in phase diagrams, the MEs display remarkable differences when examined by electrical conductivity, dynamic light scattering (DLS), small angle X-ray scattering (SAXS) and linear voltammetry. When different short-chain alcohols were employed as co-surfactants, together with sodium dodecyl sulfate (SDS) as surfactant, the DLS results indicated the systems to be monodisperse. Both the electrical conductivity of the MEs and the hydrodynamic radii of the droplets (RH) increased with water content while RH diminished as temperature increas…

ChromatographySmall-angle X-ray scatteringDispersityUltramicroelectrodeSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistrychemistryChemical engineeringDynamic light scatteringPulmonary surfactantSodium sulfateMicroemulsionSodium dodecyl sulfateJournal of colloid and interface science
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High Submicellar Liquid Chromatography

2013

Surfactant addition above the critical micellar concentration (CMC), in reversed-phase liquid chromatography (RPLC), was proposed as a way to modify the selectivity and analysis time, giving rise to a chromatographic mode called micellar liquid chromatography (MLC). However, solutions containing only surfactant are too weak and yield poor peak shape. This was remediated by the addition of a small amount of organic solvent. To preserve the existence of micelles, in MLC high contents of organic solvent are avoided. Nevertheless, there is no reason to neglect the potentiality of mobile phases containing a surfactant above its CMC in water and a high organic solvent content (without micelles). …

Chromatographycolumn interactionsElutionChemistryHydrophilic interaction chromatographyAnalytical chemistryFiltration and Separationmacromolecular substancesReversed-phase chromatographyMicelleAnalytical Chemistryreversed-phase liquid chromatographyCountercurrent chromatographyPulmonary surfactantMicellar liquid chromatographyCritical micelle concentrationchromatographic performancesubmicellar liquid chromatographySeparation & Purification Reviews
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Structural and dynamical investigation of gelation containing water-in-oil microemulsions

1996

The gelatin (Bloom 300)/water/AOT/n-heptane system has been investigated at fixed water/AOT molar ratioR (R=31.1) as a function of the gelatin content. Several experimental techniques (densitometry, refractometry, conductometry, rheology, dielectrometry, ultrasonics, hypersonics) have been used to investigate the role played by the gelatin molecule in the observed sol-gel transition above a critical gelatin content. The results appear consistent with the hypothesis of a rigid network of gelatin-water rods coated by surfactant molecules coexisting with gelatin-free AOT reversed micelles at the gelation point.

Chromatographyfood.ingredientPolymers and PlasticsConductometryChemistryConcentration effectMicelleGelatinColloid and Surface ChemistryfoodRheologyChemical engineeringPulmonary surfactantMaterials ChemistryMicroemulsionPhysical and Theoretical ChemistryRefractometryColloid and Polymer Science
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FT-IR investigation of the urea state in lecithin and sodium bis(2-ethylhexyl)phosphate reversed micelles

2003

Abstract FT-IR spectra of urea/lecithin/CCl4 and urea/sodium bis(2-ethylhexyl) phosphate (NaDEHP)/CCl4 systems as a function of the urea-to-surfactant molar ratio (Rurea) at a fixed surfactant concentration (0.1 mol kg−1) have been recorded at 25 °C. Analysis of the absorption spectra leads the to hypothesis that urea is confined within the hydrophilic micellar core of lecithin and NaDEHP reversed micelles. The encapsulation of urea involves some changes of the urea NH stretching band with respect to that of the pure solid urea, attributable to confinement effects. The stretching modes of the surfactant head group are affected by the presence of urea, indicating specific urea-surfactant hea…

Chromatographyfood.ingredientSodiumPhospholipidchemistry.chemical_elementMicelleLecithinSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryfoodSulfonatechemistryPulmonary surfactantPhosphatidylcholineUreaNuclear chemistryJournal of Colloid and Interface Science
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Confinement of chiral molecules in reverse micelles: FT-IR, polarimetric and VCD investigation on the state of dimethyl tartrate in sodium bis(2-ethy…

2008

Abstract The state of d and l -dimethyl tartrate confined within dry sodium bis(2-ethylhexyl) sulfosuccinate (AOT) reverse micelles dispersed in CCl 4 has been investigated by FT-IR spectroscopy, polarimetry, and vibrational circular dichroism (VCD). Measurements have been performed at 25 °C as a function of the solubilizate-to-surfactant molar ratio ( R ) at a fixed AOT concentration (0.158 M). The analysis of experimental data is consistent with the hypothesis that both enantiomers of dimethyl tartrate are mainly entrapped in the reverse micelles and located in proximity to the surfactant head-group region. The formation of this interesting self-organized chiral nanostructure involves som…

Circular dichroismInorganic chemistryInfrared spectroscopyTartrateMicellechemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryPulmonary surfactantVibrational circular dichroismPhysical chemistryEnantiomerDimethyl tartrate Sodium bis(2-ethylhexyl) sulfosuccinate Reverse micelles Chiral nanostructures FT-IR spectroscopy Vibrational circular dichroism Optical rotationColloids and Surfaces A: Physicochemical and Engineering Aspects
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Microemulsion encapsulated into halloysite nanotubes and their applications for cleaning of a marble surface

2018

Halloysite nanotubes were used to incorporate anionic surfactant micelles and an organic solvent to generate a cleaning system to be applied in Cultural Heritage restoration. The targeted adsorption is driven by electrostatic interactions based on the nanotubes peculiar charge separation. Namely anionic species are driven to the positively charged inner surface while being prevented from interacting with the halloysite outer surface that possesses a positive charge density. The hybrid organic/inorganic emulsion was characterized by dynamic light scattering. Analysis of the autocorrelation function allowed us to define the presence of surfactant aggregates inside/outside the nanotube lumen a…

Cleaning agentNanotubeMaterials scienceCultural heritages; Halloysite nanotubes; Polyacrylonitrile; SurfactantHalloysite nanotube02 engineering and technologyhalloysite nanotubesengineering.materialPolyacrylonitrile010402 general chemistry01 natural sciencesMicelleHalloysitelcsh:Technologylcsh:ChemistryPulmonary surfactantSurfactantGeneral Materials ScienceMicroemulsionInstrumentationlcsh:QH301-705.5Settore CHIM/02 - Chimica FisicaFluid Flow and Transfer Processeslcsh:TProcess Chemistry and TechnologyGeneral Engineeringcultural heritages021001 nanoscience & nanotechnologyElectrospinninglcsh:QC1-9990104 chemical sciencesComputer Science ApplicationsChemical engineeringlcsh:Biology (General)lcsh:QD1-999lcsh:TA1-2040EmulsionengineeringCultural heritage0210 nano-technologylcsh:Engineering (General). Civil engineering (General)lcsh:Physics
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Cloud point–dispersive μ-solid phase extraction of hydrophobic organic compounds onto highly hydrophobic core–shell Fe 2 O 3 @C magnetic nanoparticles

2012

Abstract A novel two-step extraction technique combining cloud point extraction (CPE) with dispersive micro-solid phase extraction (D-μ-SPE) is presented in this work for the first time. The method involves initial extraction of the target analytes by CPE in the micelles of a non-ionic surfactant medium; then highly hydrophobic polysiloxane-coated core–shell Fe 2 O 3 @C magnetic nanoparticles (MNPs) are used to retrieve the micellar phase. In that manner, the micellar phase containing the analytes is the target of the D-μ-SPE step rather than the analytes directly. MNPs are then collected by the application of an adscititious magnetic field overcoming the need for specific steps associated …

Cloud pointChromatographyChemistryOrganic ChemistryExtraction (chemistry)Analytical chemistryGeneral MedicineBiochemistryMicelleAnalytical ChemistryPulmonary surfactantPhase (matter)Magnetic nanoparticlesSolid phase extractionSolubilityJournal of Chromatography A
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