Search results for "salt"

showing 10 items of 1157 documents

Fractionated precipitation of acid macropolyanions by dialysis, a simple method for the estimation of DNA in complex biological samples.

1976

Abstract After efficient extraction by para-aminosalicylate, (hopping, grinding and eventual sonication, the macropolyanions are transformed into their cetyltrimethylammonium salts. These have differing solubilities, strongly depending on ionic strength. The cationic detergent-macropolyanionic salts are solubilized by high salt concentration. Salt is then dialysed out, rendering the polyanions highly insoluble in a sequential fashion. The insolubilized components are determined quantitatively by monitoring turbidity, which in case of DNA is strictly proportionate to its concentration. This relation is not affected by other components. This makes DNA determination possible even in crude aque…

chemistry.chemical_classificationAnionsChromatographyAqueous solutionPrecipitation (chemistry)TroutSonicationExtraction (chemistry)Osmolar ConcentrationSalt (chemistry)DNASaccharomyces cerevisiaeBiologyGeneral Biochemistry Genetics and Molecular BiologySoilActivated sludgechemistryIonic strengthCetrimonium CompoundsMethodsAnimalsChemical PrecipitationTurbidityDialysisZeitschrift fur Naturforschung. Section C, Biosciences
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A chiral molecular conductor: synthesis, structure, and physical properties of [ET]3[Sb2(L-tart)2].CH3CN (ET = bis(ethylendithio)tetrathiafulvalene; …

2004

The salt [ET](3)[Sb(2)(L-tart)(2)].CH(3)CN (1) has been obtained by electrocrystallization of the organic donor bis(ethylendithio)tetrathiafulvalene (ET or BEDT-TTF) in the presence of the chiral anionic complex [Sb(2)(L-tart)(2)](2-) (L-tart = (2R,3R)-(+)-tartrate). This salt crystallizes in the chiral space group P2(1)2(1)2(1) (a = 11.145(2) angstroms, b = 12.848(2) angstroms, c = 40.159(14) angstroms, V = 5750.4(14) angstroms(3), Z = 4) and is formed by alternating layers of the anions and of the organic radicals in a noncentrosymmetric alpha-type packing. This compound shows a room temperature electrical conductivity of approximately 1 S.cm(-1) and semiconducting behavior with an activa…

chemistry.chemical_classificationAntimonyChemistryStereochemistryRadicalMolecular ConformationTemperatureSalt (chemistry)Activation energyTartrateCrystallography X-RayMagnetic susceptibilityInorganic Chemistrychemistry.chemical_compoundCrystallographyElectrical resistivity and conductivityElectrochemistryOrganometallic CompoundsThermodynamicsPhysical and Theoretical ChemistryElectronic band structureTartratesTetrathiafulvaleneInorganic chemistry
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High oxidation state aqueous organometallics. Formation and structure of an oxo-centred Cp*MoV trinuclear cation by chemical reduction of Cp*2Mo2O5

2002

International audience; Reduction of Cp*2Mo2O5 by zinc/CF3CO2H in MeOH–H2O yields a salt which is composed of [Cp*3Mo3O4(O2CCF3)3]+ and [Zn2(O2CCF3)6]2− ions after crystallisation from THF–Et2O.

chemistry.chemical_classificationAqueous solution010405 organic chemistryInorganic chemistrySalt (chemistry)chemistry.chemical_elementGeneral ChemistryZinc010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesIonlaw.inventionchemistryOxidation statelaw[CHIM.CRIS]Chemical Sciences/CristallographyChemical reduction[CHIM.COOR]Chemical Sciences/Coordination chemistryCrystallizationJournal of the Chemical Society, Dalton Transactions
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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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Reversible swelling of polyanion/polycation multilayer films in solutions of different ionic strength

1996

Immersion of consecutively adsorbed polyanion/polycation multilayer films in solutions of different ionic strength causes reversible thickness changes. Swelling of the films up to 18% was observed after soaking the films in aqueous solutions of NaCl at concentrations up to 1.0 mol/l. X-ray reflectivity clearly shows that the thickness changes are reversible within experimental error and that the films seem to get smoother after several cycles of immersion in salt solutions and in pure water. The extent of swelling depends on the internal film structure, namely on the number of polyanion/polycation interfaces in a film of a given thickness. Interestingly, the swelling levels off at salt conc…

chemistry.chemical_classificationAqueous solutionChemistryGeneral Chemical EngineeringSalt (chemistry)macromolecular substancesPolymerIonAdsorptionChemical engineeringIonic strengthPolymer chemistrymedicineSelf-assemblySwellingmedicine.symptomBerichte der Bunsengesellschaft für physikalische Chemie
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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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Extraction of short peptides using supported liquid membranes

2002

Studies of extraction of short peptides using supported liquid membranes containing Aliquat 336 as a carrier are presented. The extractions are carried out from an aqueous donor phase with pH ≥ 10 to an acceptor phase containing salt. The mass transfer is driven by the gradient of salt concentration between these phases. The extraction efficiency is dependent on the composition of water phases, the type and concentration of counter-ion in the stagnant acceptor phase and the flow rate of the donor phase. Moreover, it is also influenced by the concentration and structure of the examined peptides.

chemistry.chemical_classificationAqueous solutionChromatographyMechanical EngineeringGeneral Chemical EngineeringExtraction (chemistry)Aliquat 336Salt (chemistry)General ChemistryAliquat 336Acceptorchemistry.chemical_compoundMembranechemistryMass transferPhase (matter)peptidesextractionGeneral Materials Sciencesupported liquid membraneWater Science and TechnologyDesalination
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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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Influence of some physicochemical factors on the viscosity of aqueous levan solutions ofZymomonas mobilis

1998

Zymomonas mobilis strain 113 “S” produces levan – an extracellular, viscous, biologically active, non-toxic fructose polymer with a unique structure and extraordinary properties. This polysaccharide was isolated at two different degrees of purity by alcohol precipitation from aqueous solutions and was characterized with respect to some rheological properties and stability of viscous solutions. The effects of temperature, pH and salt concentration on the viscosity of 1–3% levan solutions were examined. The viscosity of levan solutions was found to be quite stable and reversible at room temperature over a wide range of pH from 4 to 11. The viscosity was slightly affected by increased salt con…

chemistry.chemical_classificationAqueous solutionChromatographybiologyChemistryPrecipitation (chemistry)Salt (chemistry)BioengineeringPolymerbiology.organism_classificationPolysaccharideApplied Microbiology and BiotechnologyZymomonas mobilisViscosityRheologyChemical engineeringBiotechnologyActa Biotechnologica
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An electrochemical impedance and ac-electrogravimetry study of PNR films in aqueous salt media

2002

Electrochemical impedance spectra and ac-eletrogravimetry of poly(neutral red) films are studied in different aqueous media. The dependence of these experimental data on the nature of alkaline cation and monovalent anion present in the solution and on the pH is analysed. During the electrochemical processes, it is observed that all three species—the salt cation, the salt anion and the hydronium ion—participate to balance the electrical charge within the film. It is also possible to conclude that the participation of anions takes place faster than hydronium ions participation. Besides, the relative participation of these species is related to the pH of the solution. Keywords: Poly (neutral r…

chemistry.chemical_classificationAqueous solutionHydroniumInorganic chemistryAnalytical chemistrySalt (chemistry)Concentration effectElectrochemistrylcsh:Chemistrychemistry.chemical_compoundlcsh:Industrial electrochemistrylcsh:QD1-999chemistryElectrogravimetryElectrochemistryCounterionlcsh:TP250-261Electrode potential
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