Search results for "ionic strength"

showing 10 items of 198 documents

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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Solution Properties of Polyelectrolytes. VI. Secondary Effects in Aqueous Size-Exclusion Chromatography

1990

Abstract An independent analysis of different operational variables in aqueous size exclusion chromatography of poly electrolytes has been carried out using a silica-based support. The effect of polyion concentration, pH and ionic strength on sodium polystyrenesulfonate calibration plots has been investigated. Finally, a novel semi-empirical model has been developed from thermodynamic considerations which relates the support effective pore volume to the polyelectrolyte molecular weight and qualitatively describes secondary effects.

ChromatographyAqueous solutionVolume (thermodynamics)Ionic strengthChemistrySodiumSize-exclusion chromatographyMolecular Medicinechemistry.chemical_elementElectrolytePolyelectrolyteJournal of Liquid Chromatography
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Separation of selected peptides by capillary electroendoosmotic chromatography using 3 μm reversed-phase bonded silica and mixed-mode phases

1999

The retention behaviour and selectivity of selected basic, neutral and acidic peptides have been studied by capillary electroendoosmotic chromatography (CEC) with Hypersil C8, C18, Hypersil mixed-mode, and Spherisorb C18/SCX columns, 250 (335) mm x 100 microns, packed with 3 microns particles, and eluted with mobile phases composed of acetonitrile-triethylamine-phosphoric acid (TEAP) at pH 3.0 using a Hewlett-Packard Model HP3DCE capillary electrophoresis system. The selected peptides were desmopressin (D), two analogues (A and B) of desmopressin, oxytocin (O) and carbetocin (C). The peptides eluted either before or after the electroendoosmotic flow (EOF) marker, depending on the concentrat…

ChromatographyChromatographyChemistryElutionOrganic ChemistryAnalytical chemistryGeneral MedicineReversed-phase chromatographyOxytocinSilicon DioxideBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryElectrophoresisCapillary electrophoresisElectrochromatographyIonic strengthDeamino Arginine VasopressinPeptidesChromatography High Pressure LiquidStokes radiusJournal of Chromatography A
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Comparative study of Zorbax Bio Series GF 250 and GF 450 and TSK-Gel 3000 SW and SWXL columns in size-exclusion chromatography of proteins.

1988

Abstract A reduction of the mean particle diameter of silica-based packings in the size-exclusion chromatography (SEC) of proteins to about 5 μm generates the expected increase in column plate number over the traditional 10 μm SEC columns, as demonstrated for the Zorbax Bio Series GF 250 and GF 450 and TSK-Gel 3000 SWXL columns. The slightly lower column efficiency of the TSK-Gel 3000 SWXL compared with the GF 250 column is compensated by the fact that the phase ratio of the 3000 SWXL column is higher by a factor of two. Hence both columns show nearly the same peak capacity of about 20–30. When the ionic strength of the eluent was changed by varying the salt concentration, the elution volum…

ChromatographyElutionChemistryOrganic ChemistrySize-exclusion chromatographyAnalytical chemistryProteinsDextransGeneral MedicineSilicon DioxideBiochemistryAnalytical ChemistryMolecular WeightColumn chromatographyIonic strengthPhase ratioParticle diameterChromatography GelPeptidesChromatography High Pressure LiquidJournal of chromatography
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Modelling of retention behaviour of solutes in micellar liquid chromatography

1997

In micellar liquid chromatography (MLC), the resolution for a given multi-component mixture can be optimized by changing several variables, such as the concentrations of surfactant and organic modifier, the pH and temperature. However, this advantage can only be fully exploited with the development of mathematical models that describe the retention and the separation mechanisms. Several reports have appeared recently on the possibilities of accurately predicting the solute retention in MLC. Although the retention and selectivity may strongly change with varying concentrations of surfactant, organic modifier and/or pH, the observed changes are very regular, and are well described by simple m…

ChromatographyMathematical modelResolution (mass spectrometry)ChemistryOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPulmonary surfactantMicellar liquid chromatographyIonic strengthCritical micelle concentrationSelectivityJournal of Chromatography A
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Hydrolytically stable chemically bonded silica supports with metal complexating ligands: Synthesis, characterization and use in high-performance liga…

1982

A silica of 14 nm pore size was reacted according to two procedures with the following silanes: γ-aminopropyltriethoxysilane (1), N-aminoethyl-N′-aminopropyltrimethoxysilane (2), N-aminoethyl-N′-aminoethyl-N″-aminopropyltrimethoxysilane (3), N-(3-triethoxysilanepropyl)-N, N-diacetic dimethylester (4), N-(3-trisodiumsilanolatepropyl)-N, N-diacetic acid disodium salt (5) and N-(3-trisodiumsilanolatepropyl)-ethylenediamine-N, N′, N′-triacetic acid trisodium salt (6). The reaction of silanes 1–4 with the silica was carried out under anhydrous conditions (procedure A). Silanes 1–6 were subjected to surface modification under essentially hydrous conditions applying a two-step procedure (procedure…

ChromatographySilanesChemistryLigandOrganic ChemistryClinical BiochemistryInorganic chemistrySorptionBiochemistrySilaneAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyIonic strengthAnhydrousSurface modificationChromatographia
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Supported liquid membrane extraction of aromatic aminophosphonates

2001

Abstract A fast and efficient supported liquid membrane (SLM) extraction system for the series of substituted aromatic aminophosphonates was elaborated. The mass transfer of solute was examined in terms of operator (pH and ionic strength of water phase, composition of membrane phase and the concentration of analyte) dependent parameters. Additionally, the influence of the aminophosphonates structure on the extraction efficiency was examined. From the results it can be concluded that the most effective conditions of membrane process are 10% (w/w) carrier concentration (Aliquat 336) in the liquid membrane, high pH of donor phase (pH=11) and moderate salt concentration (0.4 M NaCl) in the acce…

ChromatographyaminophosphonatesChemistryExtraction (chemistry)Inorganic chemistryAliquat 336BiochemistryAcceptorAnalytical ChemistryMembrane technologychemistry.chemical_compoundMembraneIonic strengthPhase (matter)Mass transferextractionEnvironmental Chemistrysupported liquid membraneSpectroscopyAnalytica Chimica Acta
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Inducing mixing of water-in water BSA/dextran emulsion by a strong polyelectrolyte

2015

Abstract We examine whether a small amount of strong polyelectrolyte (dextran sulfate sodium salt/DSS/) can induce mixing in water-in-water bovine serum albumin/dextran (BSA/DEX) emulsion and how intermacromolecular interactions affect its the rheological properties. Addition of DSS to water-in-water emulsion at pH 5.4 leads to its mixing at the DSS/BSA weight ratio, ( q ( DSS / BSA ) ) ≥ 0.07 , a noticeable increase in viscosity and storage modulus (G′). Mixing is reversible: increasing the ionic strength leads to phase separation in the water/BSA/DEX/DSS system. The increase in viscoelasticity results from the interaction of DSS with both macromolecular compounds of the emulsion. We assum…

Chromatographybiologyanimal diseasesGeneral Chemical EngineeringGeneral ChemistryCompatibilizationdigestive systemdigestive system diseasesPolyelectrolytecarbohydrates (lipids)stomatognathic diseaseschemistry.chemical_compoundDextranchemistryChemical engineeringIonic strengthEmulsionCopolymerbiology.proteinPolymer blendBovine serum albuminFood ScienceFood Hydrocolloids
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The interaction of native calf thymus DNA with FeIII-dipyrido[3,2-a:2’,3’-c]phenazine

2008

The mono and bis dipyrido[3,2-a:2',3'-c]phenazine (dppz) adducts of iron(III) chloride, i.e. [Fe(dppz)]Cl(3) and [Fe(dppz)(2)]Cl(3), have been synthesized and characterized. The interaction of the Fe(III)dppz hydrolyzed aquo complex with native calf thymus DNA has been monitored as a function of the metal complex-DNA molar ratio, by variable temperature UV absorption spectrophotometry, circular dichroism (CD) and fluorescence spectroscopy. The results obtained in solution at various ionic strength values give support for a tight intercalative binding of the Fe(III)dppz cation with DNA. In particular, the appearance of induced CD bands, caused by the addition of Fe(III)dppz, indicate the exi…

Circular dichroismDNA dppz Intercalation Iron SpectroscopyIntercalation (chemistry)PhenazinePhotochemistryNucleic Acid DenaturationBiochemistryFerric CompoundsFluorescenceAdductInorganic ChemistryMetalchemistry.chemical_compoundDNA AdductsMetal aquo complexChemistryCircular DichroismDNABinding constantCrystallographyIonic strengthSettore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumPhenazines
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Dynamic Light Scattering Investigation of the Kinetics and Fidelity of Supramolecular Copolymerizations in Water

2017

The self-assembly of supramolecular copolymers facilitates the preparation of multifunctional materials, with tunable mechanical, electronic, or bioactive properties. Compared to covalent copolymerization protocols, controlling the molecular weight, stability, and monomer sequence of a multicomponent supramolecular copolymer remains limited. Here, we report a light scattering investigation of the charge-regulated supramolecular copolymerization in neutral buffer of physiological ionic strength, supported with electron microscopy and circular dichroism spectroscopy experiments. Dendritic anionic and cationic peptide comonomers self-assemble into AB-type heterocopolymers with a nanorod-like m…

Circular dichroismMaterials sciencePolymers and Plastics010405 organic chemistryOrganic Chemistrytechnology industry and agricultureSupramolecular chemistryCationic polymerizationmacromolecular substances010402 general chemistry01 natural sciencesLight scattering0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundMonomerDynamic light scatteringchemistryChemical engineeringIonic strengthPolymer chemistryMaterials ChemistryCopolymerMacromolecules
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