Search results for "Ionic strength"

showing 10 items of 198 documents

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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Solution properties of polyelectrolytes XII. Semi-quantitative approach to mixed electrostatic and hydrophobic polymer-gel interactions

1996

Abstract Aqueous size-exclusion chromatography of polyanions, where secondary effects affect the total separation mechanism, was investigated. For elution of polyelectrolytes on inorganic silica-based supports, the electrostatic polymer-gel repulsive interactions were evaluated through the values for a hypothetical repulsion layer, X e , according to the model developed by other workers. Using a similar procedure, the existence of an effective barrier defined as X e − X h is proposed for those systems in which electrostatic repulsion and hydrophobic interactions take place simultaneously as secondary mechanisms. X h can be viewed as a measure of the “enlargement” of the geometrical pore rad…

chemistry.chemical_classificationAqueous solutionChromatographyElutionOrganic ChemistryGeneral MedicinePolymerFlory–Huggins solution theoryElectrostaticsBiochemistryPolyelectrolyteAnalytical ChemistryHydrophobic effectchemistryIonic strengthJournal of Chromatography A
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Palladium(II) sequestration by phytate in aqueous solution. Speciation analysis and ionic medium effects.

2010

Environmental context.In the last 20 years, the demand for palladium and other platinum-group elements has intensified, causing a significant increase in their concentration in the environment, with particular accumulation in urban areas. Knowledge about Pd2+ speciation in aqueous media is fundamental for the understanding of its biological and environmental activity in contaminated areas. Phytic acid appears to be a good sequestering agent towards Pd2+ under various conditions, indicating its potential use in the remediation of contaminated sites. Abstract. Palladium(II) speciation in the presence of phytate (Phy12–) was studied by H+ ion selective electrode (ISE) potentiometry at 25°C in…

chemistry.chemical_classificationAqueous solutionMetal ions in aqueous solutionInorganic chemistryFluorescence spectrometrychemistry.chemical_elementcomplexes stability constantsPhytateIon selective electrodeDivalentMetalchemistryComplexesGeochemistry and PetrologyChemistry (miscellaneous)Ionic strengthvisual_artvisual_art.visual_art_mediumEnvironmental ChemistrySettore CHIM/01 - Chimica AnaliticaStability constantsComplexes; Stability constants; Phytate; PalladiumPalladiumPalladium
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Interactions of quinine with polyacrylic and poly-L-glutamic acids in aqueous solutions

2004

Abstract Drug-loaded polymers provide an attractive form for controlled drug delivery systems. A proper knowledge of polymer–drug interactions can aid in the designing of polymers for various drug-delivery applications. In this paper we have investigated the interaction of a drug such as quinine, with synthetic macromolecules such as poly(acrylic acid), PAA, and poly(L-glutamic acid), PGA, at pH 7 and 37 °C by fluorescence spectroscopy and viscometry. The analysis of the binding isotherms revealed that the association process is positive cooperative up to a threshold concentration and then it is negative. In addition, the thermodynamic parameters vary along the isotherm. Results also sugges…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryGeneral Physics and AstronomyPolymerPolyelectrolytechemistry.chemical_compoundChemical engineeringIonic strengthDrug deliveryMaterials ChemistryOrganic chemistryDrug carrierMacromoleculeAcrylic acidEuropean Polymer Journal
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Interaction of Alkyltin(IV) Compounds with Ligands of Interest in the Speciation of Natural fluids: Complexes of (CH3)2Sn2+ with Carboxylates

1997

Complex formation by (CH3)2Sn 2+ with acetate (ac), malonate (mal), 1,2,3-propanetricarboxylate (tricarballylate, tca) and 1,2,3,4-butanetetracarboxylate (btc) ligands in aqueous solution is reported. The study has been performed by potentiometry ([H + ]‐glass electrode) at T = 25 °C, and in the 0 < I < 1 mol dm 2 3 ionic strength range. In order to evaluate the salt effects on the formation constants of the complex species, and to contribute to the definition of the chemical speciation of diorganotin(IV) compounds in natural waters where carboxylic ligands are naturally present, interactions of NaCl (which is the major component of all natural fluids), with the components of the systems un…

chemistry.chemical_classificationAqueous solutionStereochemistrySalt (chemistry)General ChemistryDilutionInorganic Chemistrychemistry.chemical_compoundHydrolysisMalonatechemistryStability constants of complexesComputational chemistryIonic strengthCarboxylate
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Studies of the ternary systems humic substances – kaolinite – Pu(III) and Pu(IV)

2008

AbstractThe behaviour of plutonium with respect to its migration in the aquifer has been studied under conditions close to nature. Most relevant under these conditions are Pu(III) and Pu(IV) in contact with humic substances (HS) and minerals. As a model for the host rock, kaolinite (KGa-1b) was chosen. The complexation of Pu(III) and Pu(IV) with Aldrich humic acid (AHA) in aqueous solution at ionic strength 0.1 M was investigated by the ultrafiltration method. The sorption of Pu(III) and Am(III) onto kaolinite (K) as a function of pH and metal-ion concentration was studied under aerobic and anaerobic conditions. The pH edge was found at pH∼5.5 independent of the metal-ion concentration and …

chemistry.chemical_classificationAqueous solutionTernary numeral systemchemistryIonic strengthInorganic chemistryUltrafiltrationHumic acidKaoliniteSorptionPhysical and Theoretical ChemistryTernary operationNuclear chemistryRadiochimica Acta
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Equilibria involved in the diorganotin(IV) and triorganotin(IV) phosphomycin interaction in aqueous solution

2007

Four new diorganotin(IV), (R = Me, Bu), and triorganotin(IV), (R = Me, Ph), derivatives of the phosphomycin disodium salt antibiotic[(1R,2S)-1,2-epoxypropylphosphonate]Na2 have been synthesized and their solid state configuration studied by X-ray crystallography, FT-IR, Mossbauer, UV–Vis spectroscopies. The X-ray diffraction investigation, performed on the bis[trimethyltin(IV)]- phosphomycin, showed that the coordination geometry at all the Sn atoms is trigonal bipyramidal. The structure of the complex forms an unusual polymeric zig-zag planar network. The FT-IR and the 119Sn Mo¨ssbauer studies supported the formation of trigonal bipyramidal (Tbp) molecular structures, both in the diorganot…

chemistry.chemical_classificationAqueous solutionTrimethyltin(IV)LigandChemistryPotentiometric titrationInorganic chemistrySalt (chemistry)ISE-H+ potentiometric studyProtonationGeneral Chemistrydimethyltin(IV)Medicinal chemistryInorganic ChemistryFT-IRMossbauerX-rayOrganotinStability constants of complexesIonic strengthISE-H+ potentiometric study; UV–visible study; dimethyltin(IV); Trimethyltin(IV); phosphomycinUV–visible studyphosphomycinPotentiometric and spectrophotometric titrations
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Complexes of Azelaic and Diethylenetrioxydiacetic Acids with Na+, Mg2+, and Ca2+ in NaCl Aqueous Solutions, at 25 °C

1999

Formation constants of Na + , Mg 2+ , and Ca 2+ complexes of azelaic and diethylenetrioxydiacetic acids have been determined by potentiometry (H + -glass electrode) at different ionic strengths (0 ≤ I ≤ 1 mol dm -3 ), at t = 25 °C. For all the systems the species ML and MHL have been found. The relative formation constants are reported together with the parameters for the dependence on ionic strength. Results are discussed in comparison with those for other carboxylic ligands. Speciation problems are considered also.

chemistry.chemical_classificationAzelaic acidAqueous solutionGeneral Chemical EngineeringCarboxylic acidInorganic chemistryGeneral ChemistryGlass electrodelaw.inventionchemistryStability constants of complexeslawIonic strengthmedicineQualitative inorganic analysisMagnesium ionmedicine.drugJournal of Chemical &amp; Engineering Data
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Cell adhesion molecule in the hexactinellid Aphrocallistes vastus

1984

Abstract The Hexactinellida sponge Aphrocallistes vastus contains a soluble aggregation factor (AF) whose purification has been described in this communication. It is characterized by a S° 20.w value of 37 and a buoyant density of 1.45 g/cm 3 . The AF is a glycoporteinaceous particle composed of three major protein species; no core structure could be visualized. In the presence of Ca 2+ , the AF causes secondary aggregation of single cells. The aggregation process is temperature, pH, and ionic strength independent within a broad range. Evidence is presented indicating that two (or more) AF molecules are required for the establishment of a stable cell: cell interaction. In contrast to the AF…

chemistry.chemical_classificationCancer ResearchbiologyHexactinellidCell adhesion moleculeCellCell BiologyAdhesionbiology.organism_classificationSpongemedicine.anatomical_structureBiochemistrychemistryIonic strengthmedicineBiophysicsMoleculeGlycoproteinMolecular BiologyDevelopmental BiologyDifferentiation
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Modelling of natural synthetic polyelectrolyte interactions in natural waters by using SIT, Pitzer and Ion Pairing approaches

2006

Abstract In this paper SIT and Pitzer models are used for the first time to describe the interactions of natural and synthetic polyelectrolytes in natural waters. Measurements were made potentiometrically at 25 °C in single electrolyte media, such as Et 4 NI and NaCl (for fulvic acid 0.1  − 1 S single salt ” BA, with cation B and anion A representing all the major cations (Na + , K + , Mg 2+ , Ca 2+ ) and anions (Cl − , SO 4 2− ) in natural sea water, respectively. The ion pair formation model was also applied to fulvate and alginate in artificial sea water by examining the interaction of polyanions with the single sea water cation. Results were compared with those obtained from previous sp…

chemistry.chemical_classificationChemistryArtificial seawatermedia_common.quotation_subjectNatural waterInorganic chemistryArtificial seawaterSalt (chemistry)General ChemistryElectrolyteOceanographyPitzerIon Pair modelsPolyelectrolyteIonSpeciationNatural and synthetic polyelectrolytes; Specific ion Interaction Theory (SIT); Pitzer; Ion Pair models; Dependence on medium and ionic strength; Alginic and fulvic acids; Artificial seawaterDependence on medium and ionic strengthNatural and synthetic polyelectrolytesEnvironmental ChemistrySeawaterSpecific ion Interaction Theory (SIT)Alginic and fulvic acidsWater Science and Technologymedia_common
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