Search results for "Sodium"

showing 10 items of 1605 documents

Observations on the use of a sulfuric acid medium for As(V) to As(III) reduction in lodimetric titrations: Application to the determination of total …

1991

Abstract The use of a sulfuric rather than a hydrochloric acid medium for the reduction of As(V) to As(III) by iodide is proposed. Optimum conditions of acid concentration, amount of sodium hydroxide, and time and temperature are established to achieve quantitative reduction. The optimized reduction procedure was applied to the iodimetric determination of total arsenic and compared to a procedure that employs a hydrochloric acid medium. A systematic error of 0.04% was found for the method with a sulfuric acid medium opposed to 0.05% for the method with a hydrochloric acid medium in the reduction step. The proposed modified iodimetric method has been successfully used with some organic sampl…

chemistry.chemical_classificationAcid concentrationIodideInorganic chemistrychemistry.chemical_elementHydrochloric acidSulfuric acidAnalytical ChemistryReduction (complexity)chemistry.chemical_compoundchemistrySodium hydroxideTitrationSpectroscopyArsenicMicrochemical Journal
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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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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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Hydrolysis of (CH3)Hg+ in Different Ionic Media:  Salt Effects and Complex Formation

1998

The hydrolysis of monomethylmercury(II) was studied potentiometrically, in NaNO3, Na2SO4, and NaCl aqueous solution, in a wide range of ionic strengths (NaNO3, 0 ≤ I ≤ 3.25; Na2SO4, 0 ≤ I ≤ 1; NaCl, 0 ≤ I ≤ 3 mol dm-3) and at t = 25 °C. For the reaction (CH3)Hg+ = (CH3)Hg(OH)° + H+, we found log K1 = −4.528 (I = 0 mol dm-3). The species [(CH3)Hg]2(OH)+ was also found, with log β2 = −2.15. Monomethylmercury(II) forms quite strong complexes with Cl- (log K = 5.45, I = 0 mol dm-3) and SO42- (log K = 2.64, I = 0 mol dm-3). The dependence on ionic strength of formation constants was considered by using a Debye−Huckel type equation. Hydrolysis and complex formation constants (at different ionic s…

chemistry.chemical_classificationAqueous solutionChemistryGeneral Chemical EngineeringInorganic chemistryAnalytical chemistryIonic bondingSalt (chemistry)General Chemistrychemistry.chemical_compoundHydrolysisIonic strengthStability constants of complexesSodium sulfatePitzer equationsJournal of Chemical & Engineering Data
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Viscosimetric investigation of the interaction between sodium dodecylsulfate micelles and a polymer drug carrier

1993

Abstract The viscosities of aqueous sodium dodecyl sulfate solutions with and without α,β-poly( N -hydroxyethyl)- dl -aspartamide (PHEA), at 15, 25 and 35°C are reported. The viscosities of SDS and of PHEA aqueous solutions are discussed in terms of the parameter D [D = ( η η 0 − 1)/φ] describing the non-ideal behavior of SDS micelles and of PHEA macromolecules. The viscosities of SDS plus PHEA aqueous solutions, discussed in terms of the parameter F [ F = η rel ( PHEA ) + η rel ( SDS ) − η rel ( SDS + PHEA )] M , demonstrate the occurrence of interactions between SDS micelles and the PHEA macromolecule. Both D and F are scarcely influenced by temperature variation.

chemistry.chemical_classificationAqueous solutionChemistryPharmaceutical SciencePolymerMicelleDosage formchemistry.chemical_compoundPhysical chemistryOrganic chemistrySodium dodecyl sulfateDrug carrierSodium dodecylsulfateMacromoleculeInternational Journal of Pharmaceutics
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Influence of dissolved humic material and ionic strength on C8 extraction of pesticides from water

1995

A mixture of twelve intermediate polarity pesticides, mostly carbamate-type, have been chromatographied on an octadecyl-silica bonded-phase column using acetonitrile-water gradient mobile phase and UV detection. Pesticides were extracted from aqueous matrix by solid-phase extraction. The extraction system consisted of a glass microcolumn containing octyl-silica solidphase conditioned with methanol and water. The elution was by acetonitrile-dichloromethane (50:50). Studies of extraction factors like volume of sample, addition of 10% sodium chloride and presence of dissolved humic material are investigated.

chemistry.chemical_classificationAqueous solutionChromatographyElutionChemistrySodiumOrganic ChemistryClinical BiochemistryExtraction (chemistry)chemistry.chemical_elementBiochemistryAnalytical ChemistryMatrix (chemical analysis)Ionic strengthHumic acidSolid phase extractionChromatographia
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Polyelectrolytes:  Intrinsic Viscosities in the Absence and in the Presence of Salt

2008

Intrinsic viscosities were determined at 25 °C for 10 samples of narrowly distributed sodium polystyrene sulfonate (the molecular weights M ranging from 0.9 to 1000 kg/mol) in pure water and in aqueous solutions containing 0.9 wt % NaCl from the slope of ln ηrel versus polymer concentration. In the middle range of M, the [η] values are in the former case almost 2 orders of magnitude larger than in the latter case. In the absence of salt, the plot of log [η] as a function of log M exhibits a sigmoidal shape, which can be approximated within the interval 3 < M (in kg mol-1) < 30 by log[η] = −0.17 + 2.1 log M. In the presence of salt, the following relation holds true in the entire regime:  lo…

chemistry.chemical_classificationAqueous solutionChromatographyPolymers and PlasticsChemistryIntrinsic viscosityOrganic ChemistryAnalytical chemistryConcentration effectSalt (chemistry)PolymerPolyelectrolyteInorganic ChemistryMaterials ChemistryOrders of magnitude (speed)Sodium Polystyrene SulfonateMacromolecules
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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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Heat Capacity Study to Evidence the Interactions between Cyclodextrin and Surfactant in the Monomeric and Micellized States

2003

The heat capacities of transfer (ΔCpt) of hydroxypropyl-α-cyclodextrin and hydroxypropyl-γ-cyclodextrin (0.05 mol kg-1) from water to aqueous solutions of sodium hexanoate, sodium decanoate, and so...

chemistry.chemical_classificationAqueous solutionCyclodextrinInorganic chemistrySodium decanoateSurfaces and InterfacesCondensed Matter PhysicsHeat capacitychemistry.chemical_compoundMonomerchemistryPulmonary surfactantElectrochemistryOrganic chemistryGeneral Materials ScienceSodium hexanoateSpectroscopyLangmuir
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Adsorption of triblock copolymers and their homopolymers at laponite clay/solution interface. Role played by the copolymer nature

2009

The adsorption thermodynamics of copolymers, based on ethylene oxide (EO) and propylene oxide ( PO) units, at the laponite (RD) clay/liquid interface was determined at 298 K. The copolymer nature was tuned at molecular level by changing the hydrophilicity, the architecture and the molecular weight (Mw) keeping constant the EO/PO ratio. Polyethylene (PEGs) and polypropylene (PPGs) glycols with varying Mw and their mixture were also investigated to discriminate the role of the EO and the PO segments in the adsorption process. Enthalpies of transfer of RD, at fixed concentration, from water to the aqueous macromolecule solutions as functions of the macromolecule molality were determined. They …

chemistry.chemical_classificationAqueous solutionEthylene oxideGeneral Physics and AstronomyPolymerSURFACTANT INTERACTIONSANGLE NEUTRON-SCATTERINGCLAY PARTICLESHEAT-CAPACITIESBLOCK-COPOLYMERSchemistry.chemical_compoundAdsorptionchemistryChemical engineeringCONCENTRATION RANGEAQUEOUS-SOLUTIONSPolymer chemistryCopolymerPOLY(ETHYLENE OXIDE)Propylene oxideOXIDE)(13)-(PROPYLENE OXIDE)(30)-(ETHYLENE OXIDE)(13)SODIUM DODECYL-SULFATEPhysical and Theoretical ChemistryEquilibrium constantMacromoleculePhysical Chemistry Chemical Physics
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