Search results for " polyelectrolytes"

showing 4 items of 4 documents

Operational Mechanism of Conjugated Polyelectrolytes

2014

Conjugated polyelectrolytes (CPEs) are versatile materials used in a range of organic optoelectronic applications. Because of their ionic/electronic nature, characterizing these materials is nontrivial, and their operational mechanism is not fully understood. In this work we use a methodology that combines constant-voltage-driven current-density transient measurements with fast current vs voltage scans to allow decoupling of ionic and electronic phenomena. This technique is applied to diodes prepared with cationic CPEs having different charge-compensating anions. Our results indicate that the operational mechanism of these devices is governed by electrochemical doping of the CPE. On the bas…

ChemistryDopingIonic bondingNanotechnologyGeneral ChemistryBiochemistryConjugated PolyelectrolytesCatalysisIonColloid and Surface ChemistryDepletion regionDecoupling (electronics)DiodeVoltageJournal of the American Chemical Society
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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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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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