Search results for "PULMONARY"

showing 10 items of 3030 documents

Polymerizable and polymeric zwitterionic surfactants: 1. Synthesis and bulk properties

1991

Abstract The synthesis of a series of permanently zwitterionic surfactant monomers based on sulphobetaines and the preparation of their polymers is described. Solubilities, thermal properties and bulk structures of the zwitterionic polymers are studied with respect to their molecular architecture, and compared with cationic analogues. The various solubilities of the polymers can be correlated with their molecular geometry, enabling differentiation into distinct classes. This behaviour is paralleled by the observed bulk structures of the polymers where distinct classes of superstructures are present. However, independently of the molecular geometry, no thermal transition could be detected fo…

chemistry.chemical_classificationAcrylate polymerMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationCationic polymerizationPolymerchemistry.chemical_compoundMonomerMolecular geometrychemistryPulmonary surfactantPolymer chemistryMaterials ChemistrySolubilityPolymer
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Acid—base properties of azo dyes in the presence of surfactants

1991

Abstract The changes in the acid—base properties of an azo dye produced by the presence of surfactants, at surfactant concentrations below and above the CMC, are quantitatively described using a simple model and spectrophotometric and potentiometric measurements. The azo dye formed by aniline and N -(1-naphthyl)-ethylenediamine, and the surfactants sodium dodecyl sulphate, Triton X-100 and N -cetylpyridinium chloride (NCPC) are used. The protonation constants of the free and surfactant-bound dye species, the binding constant of the protonated and unprotonated forms of the dye, and the average aggregation number of the dye—NCPC aggregates are evaluated.

chemistry.chemical_classificationAggregation numberBase (chemistry)Potentiometric titrationInorganic chemistryProtonationCetylpyridinium chlorideBinding constantSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryAnilinechemistryPulmonary surfactantJournal of Colloid and Interface Science
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Structural organization of surfactant aggregates in vacuo: a molecular dynamics and well-tempered metadynamics study

2015

Experimental investigations using mass spectrometry have established that surfactant molecules are able to form aggregates in the gas phase. However, there is no general consensus on the organization of these aggregates and how it depends on the aggregation number and surfactant molecular structure. In the present paper we investigate the structural organization of some surfactants in vacuo by molecular dynamics and well-tempered metadynamics simulations to widely explore the space of their possible conformations in vacuo. To study how the specific molecular features of such compounds affect their organization, we have considered as paradigmatic surfactants, the anionic single-chain sodium …

chemistry.chemical_classificationAggregation numberChemistryMetadynamicsGeneral Physics and AstronomyIonic bondingmolecular dynamics simulations well-tempered metadynamics simulationsMicellechemistry.chemical_compoundMolecular dynamicsPulmonary surfactantChemical physicsOrganic chemistryPhysical and Theoretical ChemistrySodium dodecyl sulfateAlkylSettore CHIM/02 - Chimica Fisica
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Spatially ordered surfactant assemblies in the gas phase: negatively charged bis(2-ethylhexyl)sulfosuccinate-alkaline metal ion aggregates

2009

The formation and structural features of negatively charged aggregates of sodium bis(2-ethylhexyl)sulfosuccinate (AOTNa) surfactant molecules in the gas phase have been investigated by electrospray ionization mass spectrometry (ESI-MS) and density functional theory calculations. Mainly driven by the interactions of alkali metal ions both with the oxygen atoms of the sulfonate group and with the succinate moiety of the AOT− anion, spatially ordered supramolecular assemblies, characterized by an internal core composed of surfactant counterions and hydrophilic head groups surrounded by the surfactant alkyl chains pointing outwards, are formed. Calculations have shown that surfactant self-organ…

chemistry.chemical_classificationAggregation numberOrganic ChemistryInorganic chemistrySupramolecular chemistryHalideAlkali metalAnalytical ChemistrychemistryPulmonary surfactantMoleculeCounterionSpectroscopyAlkylRapid Communications in Mass Spectrometry
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Structural and Transport Properties of Bola C-16 Micelles in Water and in Aqueous Electrolyte Solutions

2003

Aqueous solutions containing a bolaform surfactant [R,ω-(4,7,10,13-pentaoxa-16-azacyclooctadecane)- hexadecane], with and without electrolytes have been investigated as a function of surfactant concentration and ionic strength. Small angle neutron scattering (SANS), NMR self-diffusion, and other physical-chemical methods were used. From the analysis of SANS data it was inferred that in water the surfactant forms slightly charged ellipsoidal micelles, because of the partial hydrolysis of amino groups. The aggregates grow with the increase of concentration, becoming more elongated. Due to the selective complexing ability of aza crown ether units, significant differences were observed upon add…

chemistry.chemical_classificationAqueous solutionAggregation numberChemistryInorganic chemistryElectrolyteMicellebolasSurfaces Coatings and FilmsPulmonary surfactantMicelles SANS Bolaform surfactantIonic strengthmixed surfactantssaxsCritical micelle concentrationMaterials Chemistrybolas; mixed surfactants; saxs; sdsPhysical and Theoretical ChemistrysdsCrown etherThe Journal of Physical Chemistry B
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Copolymers sensitive to temperature and pH in water and in water+oil mixtures: A DSC, ITC and volumetric study

2011

Block copolymer micelles are receiving an increasing interest because of the variety of structures and the possibilities to tune them by changing external and internal parameters achieving the desired properties for a specific purpose. We have investigated the acid/base behavior, self-assembling and solubilization ability towards polar oils of star-like copolymers named Tetronics. They are composed of branched four-arms each one consisting of two blocks made of EO and PO units linked to the diethylenediamine group, which confers pH response ability. The copolymers T1107 and T90R4 were studied with a sequential and reverse architecture. The thermodynamics of the acid/base equilibrium was stu…

chemistry.chemical_classificationAqueous solutionBase (chemistry)ChemistryCopolymers DSC ITC solubilizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistryDifferential scanning calorimetryMolar volumeChemical engineeringPulmonary surfactantCopolymerOrganic chemistryMacromoleculeJournal of Colloid and Interface Science
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Transfer of Some Alkyl Substituted Ferrocenes from Water to Cationic Surfactant Micelles Studied by Kinetic Method

1994

Abstract Binding of ferrocene and its 1,1′-dimethyl and n -butyl derivatives to dodecyl and tetradecyltrimethylammonium nitrate micellar aggregates has been studied at 20.0°C and ionic strength 0.02 tool dm -3 by examining the micellar retarding effects on the rates of iron(III) oxidation of these substrates. Solubilization of the ferrocenes in the cationic micellar phase increases as the substrate hydrophobic character increases and, to a lesser extent, as the surfactant hydrocarbon chain length becomes longer. The critical micelle concentrations of the surfactants used and the incremental free energy of transfer of methylene groups of both the substrate and the surfactant from the aqueous…

chemistry.chemical_classificationAqueous solutionChemistryInorganic chemistryCationic polymerizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantFerroceneIonic strengthMethyleneAlkylJournal of Colloid and Interface Science
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Quasi-elastic light scattering in polymer-containing microemulsion

1996

Abstract Quasi-elastic light scattering (QELS) was performed in dilute water in oil microemulsion stabilized by AOT surfactant. The water-soluble polyethylene oxide (PEO) with low molecular weight (8000) added to the microemulsion seems to be confined within the aqueous microphase, since PEO is insoluble in oil (n-heptane). The measurements by QELS of diffusion coefficient, at dilute concentrations, allow determination of the size of the droplets. The phase diagram of the microemulsion undergoes remarkable changes on addition of the polymer. The results show that at fixed R ( water surfactant ratio) the droplets decrease their size as the concentration of polymer increases. This occurrence …

chemistry.chemical_classificationAqueous solutionChromatographyHydrodynamic radiusDiffusionOrganic Chemistrytechnology industry and agriculturePolymerLight scatteringAnalytical ChemistryInorganic ChemistryReduced propertieschemistryPulmonary surfactantChemical engineeringMicroemulsionSpectroscopyJournal of Molecular Structure
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Chromatography of metal chelates

1973

The chromatographic behavior of metal bis(ethoxyethyl)dithiocarbamate was investigated. The chelates of 14 elements (V, Cr, Co, Ni, Cu, Zn, Se, Mo, Cd, Te, Hg, Tl, Pb and Bi) could be preconcentrated from water with an on-line system and were shown to be suitable for C18-reversed-phase liquid chromatography. A quaternary solvent mixture with admixture of a surfactant was used as eluent, UV-detection was performed at 254 nm. Thermostating the column to 40° C resulted in a significant increase in chromatographic resolution and in a decrease of analysis time. The recovery of the chelates from the aqueous solutions as well as reproducibility of the results are very sensitive to pH changes.

chemistry.chemical_classificationAqueous solutionChromatographyResolution (mass spectrometry)Clinical BiochemistryGeneral MedicineBiochemistryAnalytical ChemistryMetalSolventColumn chromatographychemistryPulmonary surfactantvisual_artvisual_art.visual_art_mediumGeneral Materials ScienceChelationDithiocarbamateFresenius' Zeitschrift f�r Analytische Chemie
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Characterization of the Cyclodextrin−Surfactant Interactions by Volume and Enthalpy

2003

Volume and enthalpy of transfer of hydroxypropyl-α-cyclodextrin (HP-α-CD) and hydroxypropyl-γ-cyclodextrin (HP-γ-CD) from water to the aqueous solutions of sodium alkanoates (sodium hexanoate, sodium decanoate and sodium dodecanoate) were determined at 298 K. The cyclodextrin concentration was kept constant, and that of the surfactant was varied in order to analyze both the pre- and postmicellar regions. The experimental data in the premicellar region were consistent with the formation of 1:1 and 1:2 (1 cyclodextrin:2 surfactants) inclusion complexes, with the exception of the HP-α-CD/sodium dodecanoate system which presented only the 1:1 complexes. The mechanism of the 1:2 complexes format…

chemistry.chemical_classificationAqueous solutionCyclodextrinChemistrySodiumEnthalpyInorganic chemistrychemistry.chemical_elementSodium decanoateSurfaces Coatings and Filmschemistry.chemical_compoundPulmonary surfactantMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryQuantitative analysis (chemistry)The Journal of Physical Chemistry B
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