Search results for "Strength"

showing 10 items of 2415 documents

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
researchProduct

Solution properties of polyelectrolytes

1993

Abstract Aqueous size-exclusion chromatography was used to analyse the elution behaviour of several standard ionic polymers, including poly( l -glutamic acid), sodium poly(styrene sulphonate) and poly(acrylic acid), different in nature and chain flexibility, as a function of the pH and ionic strength of the eluent. Two organic-based hydrophilic packings, Spherogel TSK PW4000 and Ultrahydrogel 250, were tested in order to select the optimal conditions of macromolecular separation, and the results obtained for each column were compared. A set of calibration graphs for the above polyions as a function of eluent pH and ionic strength were obtained and compared with those obtained for uncharged …

chemistry.chemical_classificationAqueous solutionChromatographyChemistryElutionOrganic ChemistrySize-exclusion chromatographyIonic bondingPolymerGeneral MedicineElectrostaticsBiochemistryPolyelectrolyteAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundColumn chromatographyIonic strengthSurface chargeAcrylic acidJournal of Chromatography A
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

p-Nitrophenolate: A Probe for Determining Acid Strength in Ionic Liquids

2009

In order to obtain an acidity scale in room-temperature ionic liquid solutions, the protonation equilibrium of sodium p-nitrophenolate in [bm(2)im][NTf(2)] and in [bmpyrr][NTf(2)], at 298 K, has been studied by means of spectrophotometric titration. Carboxylic acids differing in both structure and in water solution strength have been used. Data collected indicate that in the analyzed ionic liquid solutions carboxylic acids are less dissociated than in water solution. Furthermore, by virtue of a mutual interaction, the studied equilibrium seems to be affected by both the nature of the ionic liquids and the carboxylic acids.

chemistry.chemical_classificationAqueous solutionMolecular StructureCarboxylic acidOrganic ChemistryInorganic chemistryCarboxylic AcidsIonic LiquidsWaterProtonationSettore CHIM/06 - Chimica OrganicaHydrogen-Ion ConcentrationNitrophenolsSolutionsAcid strengthNitrophenolchemistry.chemical_compoundchemistryIonic Liquids Carboxylic acids Acidity measurementsIonic liquidMoleculeTitrationThe Journal of Organic Chemistry
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct