Search results for "ALK"

showing 10 items of 4314 documents

Molecular dynamics of electrosprayed water nanodroplets containing sodium bis(2-ethylhexyl)sulfosuccinate

2013

The behavior of aqueous solutions of sodium bis(2-ethylhexyl)sulfosuccinate (AOTNa) subject to electrospray ionization (ESI) has been investigated by molecular dynamics (MD) simulations at three temperatures (350, 500 and 800 K). We consider several types of water nanodroplets containing AOTNa molecules and composed of a fixed number of water molecules (1000), N(AOT)(0) AOT(-) anions (N(AOT)(0) =  0, 5, 10) and N(Na)(0) sodium ions (N(Na)(0) =  0, 5, 10, 15, 20): in a short time scale (less than 1 ns), the AOTNa molecules, initially forming direct micelles in the interior of the water nanodroplets, are observed in all cases to diffuse nearby the nanodroplet surface, so that the hydrophilic …

chemistry.chemical_classificationAqueous solutionChemistryElectrospray ionizationSodiumAnalytical chemistryAnhydrousMoleculechemistry.chemical_elementMicelleSpectroscopyAlkylIonJournal of Mass Spectrometry
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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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Speciation of polyelectrolytes in natural fluids Protonation and interaction of polymethacrylates with major components of seawater.

2002

Acid–base properties of two sodium polymethacrylates (W= 4000 and 5400 Da) were studied potentiometrically in aqueous solution at 25 °C. Measurements were made in different salt solutions: LiCl 0.1–1.5, NaCl 0.1–2, KCl 0.1–2, Et4NI 0.1–0.75 mol l − 1 , and in artificial seawater in the salinity range 10 S 45. Protonation data were analysed by two different models and the dependence of the relative parameters on ionic strength were calculated. Measurements performed in interacting media (alkali metal chlorides and artificial seawater) were interpreted in terms of complex formation, and the relative formation parameters are reported. Previous data on the interaction of a higher molecular weig…

chemistry.chemical_classificationAqueous solutionChemistryIonic strengthInorganic chemistrySalt (chemistry)Artificial seawaterProtonationSeawaterAlkali metalPolyelectrolyteAnalytical ChemistryTalanta
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Calorimetric study on the solubilization of some primary alcohols by reversed AOT micelles

1989

A calorimetric method to evaluate, at the same time, the distribution constant and the standard enthalpy of transfer of a solute partitioned between organic phase and reversed micelles is proposed. The method was applied to the partition of methanol, 1-propanol and 1-pentanol between n-heptane and AOT reversed micelles containing water at 25°C. The results show that the distribution constant decreases as the alcohol alkyl chain length increases and that the solubilization site can change as the water content of reversed AOT micelles increases. In particular, at sufficiently high water content, methanol seems to be preferably solubilized in the aqueous pseudophase whereas 1-pentanol prefers …

chemistry.chemical_classificationAqueous solutionChromatographyChemistryEnthalpyDistribution constantInorganic chemistryBiophysicsPrimary alcoholBiochemistryMicellePartition coefficientchemistry.chemical_compoundMethanolPhysical and Theoretical ChemistryMolecular BiologyAlkylJournal of Solution Chemistry
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Thermodynamic Evidence of Cyclodextrin−Micelle Interactions

2002

The enthalpy of transfer (ΔHt) of hydroxypropyl-α-cyclodextrin (HP-α-CD), hydroxypropyl-β-cyclodextrin (HP-β-CD), and β-cyclodextrin (β-CD) from water to the aqueous C6F13CO2Na and C7F15CO2Na solutions were determined in the pre- and post-micellar regions. The behavior of the macrocycles is system specific. Generally, the magnitude of the enthalpy is influenced by several factors:  (1) the alkyl chain length of the surfactant, (2) the cyclodextrin cavity and its alkylation, (3) the interactions between the free cyclodextrin and the free surfactant, (4) the host−guest equilibrium constant, (5) the host/guest stoichiometry, and (6) the micelle-cyclodextrin (free and/or complexed) interactions…

chemistry.chemical_classificationAqueous solutionCyclodextrinEnthalpyAlkylationMicelleSurfaces Coatings and FilmsCrystallographychemistryPulmonary surfactantMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryEquilibrium constantAlkylThe Journal of Physical Chemistry B
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Enthalpies of Mixing of Some Primary Hydrogenated and Fluorinated Alcohols and Sodium Dodecanoate Aqueous Solutions

1993

Abstract The enthalpies of transfer from water to the surfactant solutions ΔH(W → W + S) of some hydrogenated and fiuorinated alkanols and of sodium dodecanoate NaL were determined. In the premicellar region the measurements were carried out as functions of both the additive and the surfactant concentrations in order to evaluate the interaction parameters between the additive and the surfactant molecules. It is shown that in this region, pair, triplet, and quadruplet interaction parameters between unlike solute molecules contribute to ΔH(W → W + S). Within the large uncertainty with which these parameters are determined because of the very narrow surfactant and alcohol concentration interva…

chemistry.chemical_classificationAqueous solutionDistribution constantEnthalpyConcentration effectSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsPropanolchemistry.chemical_compoundColloid and Surface ChemistrychemistryPulmonary surfactantPhysical chemistryOrganic chemistryAlkylHexanolJournal of Colloid and Interface Science
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Heat capacities, volumes and solubilities of pentanol in aqueous alkyltrimethylammonium bromides

1988

Apparent molar heat capacities and volumes of pentanol, 0.05m in decyl-, tetradecyl- and hexadecyltrimethylammonium bromides micellar solutions, were measured at 25°C. They were assumed to approach the standard infinite dilution values and rationalized by means of previously reported equations following which the distribution constant between the aqueous and the micellar phase, heat capacity, and volume of pentanol in both phases are simultaneously derived. The present results show that the volume of the micellar core does not seem to have a significant effect on the apparent molar volume and heat capacity of pentanol in the micellar phase and on the free energy of transfer of pentanol from…

chemistry.chemical_classificationAqueous solutionDistribution constantInorganic chemistryBiophysicsThermodynamicsBiochemistryHeat capacityMolar volumechemistryPhase (matter)Micellar solutionslipids (amino acids peptides and proteins)Physical and Theoretical ChemistrySolubilityMolecular BiologyAlkylJournal of Solution Chemistry
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Alkaline Pre-treatment of Hardwood Chips Prior to Delignification

2013

Scots pine (Pinus sylvestris) chips were pre-treated with alkaline solutions (alkali charges of 1, 2, 3, 4, 6, and 8% of NaOH on the oven-dried wood material) at 130°C and 150°C for various treatment times (30, 60, 90, and 120 minutes). Under these conditions, 2.0–13.6% of the wood d.s. was dissolved into the aqueous hydrolysates. The soluble organic fraction was primarily characterized in terms of carbohydrates (monosaccharides and oligo-/polysaccharides) and their alkali-catalyzed degradation products: aliphatic carboxylic acids containing, besides non-volatile hydroxy carboxylic acids, volatile formic and acetic acids. With increasing alkali charge, temperature, and time, the enhanced fo…

chemistry.chemical_classificationAqueous solutionGeneral Chemical EngineeringGeneral ChemistryPolysaccharideAlkali metalHydrolysatechemistry.chemical_compoundchemistryHardwoodDegradation (geology)Organic chemistryMonosaccharideLigninGeneral Materials Scienceta116Journal of Wood Chemistry and Technology
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Bimolecular reduction of 9-alkyl-3-nitrocarbazoles

2007

AbstractReduction of 9-alkyl-3-nitrocarbazoles (Ia–Ie) with lithium aluminium hydride gave corresponding 9,9′-dialkyl-3,3′-azocarbazoles (IIa–IIe) in moderate yield. By the action of zinc dust in alcohol and aqueous alkali on I or II, 5,13-dialkyldiindolo[3,2-a,d]phenazines (IIIa–IIId) were obtained. Parent compounds, viz. 3,3′-azocarbazole (IIf) and diindolo[3,2-a,d]phenazine (IIIf) could not be obtained in these ways. Compound IIf was obtained in Vorländer reaction and IIIf by thermal decomposition of 3-azidocarbazole. Formation of IIIa–IIId is explained as a result of ortho-benzidine rearrangement of hypothetical 9,9′-dialkyl-3,3′-hydrazocarbazoles.

chemistry.chemical_classificationAqueous solutionGeneral Chemical EngineeringThermal decompositionInorganic chemistryPhenazineAlcoholGeneral ChemistryLithium aluminium hydrideAlkali metalBiochemistryMedicinal chemistryIndustrial and Manufacturing Engineeringchemistry.chemical_compoundchemistryYield (chemistry)Materials ChemistryAlkylChemical Papers
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Free energy of transfer ofn-nitroalkanes fromn-octane to water at 25�C

1983

Calorimetric determinations of the thermodynamics of transfer of nitromethane, nitroethane, 1-nitrobutane, 1-nitropentane, and 1-nitrohexane from n-octane to water at 25°C have been made. Transfer free energies calculated by four different models agree reasonably well with observations. Calculations indicate that the dipolar part of the transfer free energy depends only on the dipole moment and size of the-C−NO2 group and is independent of the length of the alkyl chain in nitroalkanes.

chemistry.chemical_classificationAqueous solutionNitromethaneBiophysicsBiochemistryDipoleTransfer (group theory)chemistry.chemical_compoundchemistryMoment (physics)NitroethanePhysical chemistryPhysical and Theoretical ChemistryMolecular BiologyAlkylOctaneJournal of Solution Chemistry
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