Search results for "Electrolyte"

showing 10 items of 746 documents

Isobaric Vapor−Liquid Equilibria for 1-Propanol + Water + Calcium Nitrate

1999

Isobaric vapor−liquid equilibria for all of the binary and ternary mixtures of 1-propanol, water, and calcium nitrate have been measured at 100.00 kPa using a recirculating still. The addition of calcium nitrate to the solvent mixture produced an important salt effect; the azeotrope was removed at salt mole fractions higher than 0.08. The three experimental binary data sets were independently fitted with the electrolyte NRTL model (Mock, B.; Evans, L. B.; Chen, C. C. AIChE J. 1986, 32, 1655−1664), and the parameters of Mock's model were estimated for each binary system. No ternary parameter was required. These parameters were used to predict the ternary vapor−liquid equilibrium using the sa…

ChromatographyGeneral Chemical EngineeringThermodynamicsGeneral ChemistryElectrolyteMole fractionCalcium nitratechemistry.chemical_compoundchemistryAzeotropeNon-random two-liquid modelIsobaric processBinary systemTernary operationJournal of Chemical & Engineering Data
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Isobaric Vapor−Liquid Equilibria for Water + Acetic Acid + Lithium Acetate

2001

Isobaric vapor−liquid equilibria for all of the binary and ternary mixtures of water, acetic acid, and lithium acetate have been measured at 100.00 kPa using a recirculating still. To take into account the association of the acetic acid in the vapor phase, Marek's chemical theory has been considered. The three experimental binary data sets have been independently correlated using Mock's electrolyte NRTL model, and the binary parameters estimated for each binary system have been used to predict the ternary vapor−liquid equilibrium using the same model. No ternary parameters were required. The ternary equilibrium values obtained in this way agreed well with the experimental values.

ChromatographyGeneral Chemical EngineeringThermodynamicsGeneral ChemistryLithium acetateElectrolyteAcetic acidchemistry.chemical_compoundchemistryBinary dataNon-random two-liquid modelIsobaric processBinary systemTernary operationJournal of Chemical & Engineering Data
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Ionomers in solution: 1. Viscometric and chromatographic studies in cononsolvent and cosolvent mixtures

1997

Abstract The viscosity and elution behaviour of polystyrene sulfonate ionomers with varying ionic content has been studied in the pure solvents chloroform (CHL), tetrahydrofuran (THF), dioxan (DIO), ethyl acetate (EA) and dimethylformamide (DMF) as well as in their cononsolvent mixtures CHL/THF (50:50), DIO/CHL (75:25) and in the cosolvent mixture EA/DMF (50:50). In the pure solvents with low dielectric constant the reduced viscosities of ionomers are lower at low concentrations and higher at moderate ones than the respective viscosities of the polystyrene precursor. These results can be explained by formation of intramolecular and intermolecular associations. Moreover, differences in visco…

ChromatographyPolymers and PlasticsOrganic ChemistryConcentration effectIonic bondingPolyelectrolytePolystyrene sulfonatechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryDimethylformamidePolystyreneIonomerTetrahydrofuranPolymer
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Determination of water-soluble vitamins in energy and sport drinks by micellar electrokinetic capillary chromatography

2016

Abstract A method for the determination of water-soluble vitamins in several energy and sport drinks by micellar electrokinetic chromatography (MEKC) has been developed in this work. The separation of vitamins was studied in terms of background electrolyte composition (borate content, pH, surfactant type and content) and in other MEKC parameters. A study of the possible compounds found in the vitamin-enriched drinks that could interfere in vitamin determination was also performed, and a modified procedure with enhanced resolution was developed. The proposed method was successfully applied to the analysis of water-soluble vitamins in a variety of energy and sport drinks and also in fruit nec…

ChromatographyResolution (mass spectrometry)Chemistry010401 analytical chemistry04 agricultural and veterinary sciences040401 food science01 natural sciencesMicellar electrokinetic chromatography0104 chemical sciences0404 agricultural biotechnologyPulmonary surfactantReagentWater-Soluble VitaminSample preparationElectrolyte compositionSoft drinkFood ScienceBiotechnologyFood Control
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Measurement of the Md3+/Md2+ Reduction Potential Studied with Flow Electrolytic Chromatography

2013

The reduction behavior of mendelevium (Md) was studied using a flow electrolytic chromatography apparatus. By application of the appropriate potentials on the chromatography column, the more stable Md(3+) is reduced to Md(2+). The reduction potential of the Md(3+) + e(-) → Md(2+) couple was determined to be -0.16 ± 0.05 V versus a normal hydrogen electrode.

ChromatographyStandard hydrogen electrodeFlow (psychology)Analytical chemistrychemistry.chemical_elementElectrolyteIonMendeleviumInorganic ChemistryReduction (complexity)chemistryPhysical and Theoretical ChemistryLuminescenceChromatography columnInorganic Chemistry
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Determination of rate constants of ion transfer kinetics across immiscible electrolyte solutions

1998

Abstract The rotating diffusion cell was used to study ion transfer across the interface between two immiscible electrolyte solutions. Tetrabutylammonium was chosen as the transferring cation and lithium chloride as the supporting electrolyte in aqueous phase. Tetrabutylammonium tetrakis-(4-fluorophenyl)-borate in 2-nitrophenyl-octylether was used as the organic electrolyte solution supported in the porous membrane. The quasi-steady state current–voltage curves were measured both by applying potential steps and by imposing a slow potential sweep. The analysis of experimental results was based on the comparison with the theoretical current–voltage curves and on the Koutecky–Levich plots. The…

ChromatographySupporting electrolyteGeneral Chemical EngineeringAqueous two-phase systemThermodynamicsConcentration effectElectrolytechemistry.chemical_compoundReaction rate constantElectrical resistance and conductancechemistryElectrochemistryLithium chlorideITIESElectrochimica 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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Einflu� eines diphenolischen Laxans (Bisacodyl) auf den Wasser- und Elektrolyttransport im menschlichen Colon

1974

Bei 5 Versuchspersonen wurde die Wirkung von Bisacodyl auf die Wasser- und Elektrolytbewegungen im menschlichen Colon untersucht. Das Colon wurde durch eine Sonde perfundiert, die in das Coecum plaziert wurde. Die Perfusionslosung enthielt NaCl (140 maq/l) als Chlorid und Bicarbonat und K (2,8 maq/l) als Chlorid sowie14C-Polyathylenglykol als Marker. Sie wurde mit einer Rate von 10 ml/min perfundiert und uber ein Darmrohr im Rectum wieder aufgefangen.

Chromatographymedicine.medical_treatmentPotassiumSodiumLaxativechemistry.chemical_elementCatharticGeneral MedicineElectrolytechemistryDrug DiscoverymedicineMolecular MedicineWater-Electrolyte BalanceBisacodylGenetics (clinical)Human colonmedicine.drugKlinische Wochenschrift
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Enantiomeric separation of chiral phenoxy acid herbicides by electrokinetic chromatography. Application to the determination of analyte-selector appa…

2001

The enantiomeric resolution of chiral phenoxy acid herbicides was performed by electrokinetic chromatography using a cyclodextrin as chiral pseudophase (CD-EKC). A systematic evaluation of several neutral and charged cyclodextrins was made. Among the cyclodextrins tested, (2-hydroxy)propyl beta-cyclodextrin (HP-beta-CD) was found to be the most appropriate for the enantioseparation of phenoxy acids. The influence of some experimental conditions, such as nature and pH of the background electrolyte, chiral selector concentration, and temperature, on the enantiomeric separation of phenoxy acids was also studied. The use of a 50 mM electrolyte solution in ammonium formate at pH 5 and a temperat…

CienciaAnalyteElectrokinetic chromatographyResolution (mass spectrometry)ScienceChemistry analytic and technicalClinical BiochemistryElectrolytePhenoxy acid herbicidesBiochemistryAnalytical ChemistryElectrolyteschemistry.chemical_compoundElectrokinetic phenomenaTwo temperatureCIENCIAAmmonium formateOrganic chemistrychemistry.chemical_classificationChromatographyCyclodextrinsChromatographyCyclodextrinHerbicidesChemistryPhenyl Ethersbeta-CyclodextrinsTemperatureStereoisomerismQuímica analítica e industrialSCIENCEHydrogen-Ion Concentration2-Hydroxypropyl-beta-cyclodextrinSolutionsPropionatesEnantiomerELECTROPHORESIS
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Titration of poly(dA-dT) · poly(dA-dT) in solution at variable NaCl concentration

2004

CD and uv absorption data showed that high molecular weight poly(dA-dT) . poly(dA-dT), at 298 K, undergoes an acid-induced transition from B-double helix to random coil in NaCl solutions of different concentrations, ranging from 0.005 to 0.600M. Similarly, titration of the polynucleotide with a strong base causes duplex-to-single strands transition. The base- and acid-induced transitions were both reversible by back-titration (with an acid or, respectively, with a base): the apparent pKa were the same in both directions. However, the number of protons per titratable site (adenine N1) required to reach half-denaturation was in great excess over the stoichiometric value; to a much larger exte…

Circular dichroismOrganic ChemistryBiophysicsGeneral MedicineBiochemistryPolyelectrolyteRandom coilThymineBiomaterialsCrystallographychemistry.chemical_compoundDeprotonationchemistryPolynucleotideCounterion condensationOrganic chemistryTitrationBiopolymers
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