Search results for " Ionic strength"

showing 7 items of 17 documents

Evaluation of the sequestering ability of different complexones towards Ag+ ion

2014

Abstract The interaction between Ag+ cation and different ligands was evaluated as a function of temperature and ionic strength by means of potentiometric techniques. Six aminopolycarboxylic (APCs) and aminopolyphosphonic (APPs) ligands were chosen, namely four APCs: nitrilotriacetic acid (NTA), ethylene-glycol-bis(2-aminoethylether)-N,N,N’,N’-tetraacetic acid (EGTA), ethylenediamine-N,N,N’,N’-tetraacetate (EDTA) and diethylenetriamine-N,N,N’,N”,N”-pentaacetic acid (DTPA)] and two APPs: [(1-hydroxyethane-1,1-diyl)bis(phosphonic acid) (HEDP) and [[(Phosphonomethyl)imino]bis[2,1-ethanediylnitrilobis(methylene)]] tetrakis-phosphonic acid (DTPP). Different mononuclear species with general formu…

LigandPotentiometric titrationInorganic chemistryNitrilotriacetic acidCondensed Matter PhysicsSilver aminipolycarboxylates aminopolyphosphonates ionic strength sequestration.Atomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsIonMetalchemistry.chemical_compoundchemistryStability constants of complexesIonic strengthvisual_artMaterials Chemistryvisual_art.visual_art_mediumSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryMethyleneSpectroscopy
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Modelling of natural and synthetic polyelectrolyte interactions in natural waters.

2006

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 Et4NI and NaCl (for fulvic acid 0.1 < I /mol L− 1 < 0.75), and in a multi-component medium simulating the composition of natural waters at a wide range of salinities (for fulvic and alginic acids: 5 < S < 45) with particular reference to sea water [Synthetic Sea Water for Equilibrium studies, SSWE]. In order to simplify calculations, SSWE was considered to be a “single salt” BA, with cation B and anion A representing all the major cations (Na+, K+, Mg2+…

Natural and synthetic polyelectrolytes: SITion pair modelDependence on medium and ionic strengthArtificial seawaterdependence on medium and ionic strength: alginic and fulvic acidNatural and synthetic polyelectrolytesSpecific ion Interaction Theory (SIT)PitzerIon Pair modelsAlginic and fulvic acids
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Iontophoretic Transdermal Delivery of Sumatriptan: Effect of Current Density and Ionic Strength

2005

ABSTRACT: Iontophoretic transdermal delivery of sumatriptan was investigated in vitro . Among the conditions tested, 0.25 mA/cm 2 and low ionic strength (NaCl 25 mM) was the best experimental condition to increase its transport across the skin. The flux increased 385-fold respective to passive diffusion, thus resulting in a transdermal flux of sumatriptan of 1273 ± 83 nmol/cm 2 h. © 2005 Wiley-Liss, Inc. and the American Pharmacists Association

OsmosisTime FactorsSwineSkin AbsorptionDiffusionPharmaceutical ScienceBuffersSodium ChloridePharmacologyAdministration CutaneousPharmaceutical technologymedicineAnimalsSkinTransdermalIontophoresisSumatriptanChemistryOsmolar ConcentrationEarIontophoresisLow ionic strengthSerotonin Receptor AgonistsSumatriptanIonic strengthCurrent densitymedicine.drugBiomedical engineeringJournal of Pharmaceutical Sciences
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Zr, Hf and REE distribution in river water under different ionic strength conditions

2018

International audience; The Platani River flowing in south-central Sicily, interacting with evaporite rocks, generates a wide range of ionic strength in the water catchment from 0.1 to 5.0 mol kg−1. We sampled 38 river sites and analysed the composition for the dissolved fraction filtered through 0.45 μm, the truly dissolved fraction obtained through ultrafiltration (10 kDa) and the relative included colloidal fraction.This study was focused on the recognition of Zr, Hf and REE behaviour under changing ionic strength conditions, since this is one of parameters responsible for colloid stability in natural waters. In turn, this phenomenon leads to REE release from the colloidal fraction and t…

River colloidsEnvironmental EngineeringRare Earth Elements010504 meteorology & atmospheric sciencesUltrafiltrationAnalytical chemistry010502 geochemistry & geophysics01 natural sciencesColloidchemistry.chemical_compoundIonic strength[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryEnvironmental ChemistryZr/HfWaste Management and DisposalScavenging0105 earth and related environmental sciencesRiver colloids Rare Earth Elements Zr/Hf Ionic strengthSedimentAuthigenicPollution6. Clean waterSettore GEO/08 - Geochimica E VulcanologiachemistryIonic strength[SDE]Environmental SciencesCarbonateSeawater
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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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On the Complexation of Cu(II) and Cd(II) With Polycarboxyl Ligands. Potentiometric Studies With ISE-H+, ISE-Cu2+, and ISE-Cd2+

2009

The interaction of Cu2+ and Cd2+ ions with polyacrylates (PAA, 2 kDa and 100 kDa), polymetacrylate(PMA, 5.4 kDa), and alginate (AA, 70 kDa to 100 kDa) was studied by potentiometry, using ISE-Cu2+, ISE-Cd2+, and ISE-H+ electrodes. The investigations were performed in NaNO3 aqueous solutions, in the ionic strength range 0.10 e I (mol ·L-1) e 0.75, at T ) 298.15 K. The “diprotic-like model” was used to explain the acid-base behavior of the polycarboxylates under investigation (for this model, the monomeric unit of the polyelectrolyte is considered as a dicarboxylate). The results give evidence for the formation of the ML species in all the systems investigated. In addition, the MLH species was…

inorganic chemicalsAcrylate polymerchemistry.chemical_classificationSequestering abilitypolycarboxylic acidsLigandGeneral Chemical EngineeringIonic strength dependencePotentiometric titrationInorganic chemistryGeneral ChemistryUronic acidComplexation Potentiometric study polyelectrolytesPolysaccharidePolyelectrolytechemistry.chemical_compoundchemistryIonic strengthSodium nitrateSettore CHIM/01 - Chimica Analiticapolycarboxylic acids; Sequestering ability; Ionic strength dependenceNuclear chemistryJournal of Chemical &amp; Engineering Data
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Speciation of dimethyltin(IV) – and trimethyltin(IV) – carbocysteinate and – glutamate systems in aqueous media

2008

The formation of complex species in the dimethyltin(IV) and trimethyltin(IV)-carboxymethyl-L-cysteinate (carbocysteinate) systems in NaClaq, at different ionic strengths, and in a multicomponent Na+, K+, Ca2+, Mg2+, Cl- and SO42- medium representative of the seawater major composition, is discussed. Experimental results give evidence for the formation of the following species (L¼carbocysteinate): [(CH3)2Sn(L)]0, [(CH3)2Sn(HL)]+, [(CH3)2Sn(OH)(L)]-, [(CH3)2Sn(OH)2(L)]2- in the DMT–CCYS system, and [(CH3)3Sn(HL)]0, [(CH3)3Sn(L)]- and [(CH3)3Sn(OH)(L)]2- in the TMT-CCYS system. The ionic strength dependence of formation constants was taken into account by an extended Debye Huckel type equation…

organotin(IV) compounds; carboxymethyl-L-cysteinate; glutamateChemical Health and SafetyAqueous mediumChemistrydependence on ionic strength of formation constantHealth Toxicology and Mutagenesismedia_common.quotation_subjectInorganic chemistryComplex formationorganotin(IV) compoundGlutamate receptormixed ionic mediaIonic bondingglutamateToxicologycarboxymethyl-L-cysteinateSpeciationspeciationcomplex formationOrganic chemistrySettore CHIM/01 - Chimica Analiticamedia_commonChemical Speciation &amp; Bioavailability
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