Search results for "electrolyte"

showing 10 items of 746 documents

The CEC behaviour of several synthetic peptides related to the activin ��A-��D subunits

2008

The resolution of several structurally related synthetic peptides, derived from the loop 3 region of the activin betaA-betaD subunits, has been studied using capillary electrochromatography (CEC) with Hypersil n-octadecylsilica as the sorbent. The results confirm that the CEC migration of these peptides can be varied in a charge-state-specific manner as the properties of the background electrolyte, such as pH, salt concentration and content of organic modifier, or temperature are systematically changed. Acidic peptides followed similar trends in retention behaviour, which was distinctly different to that shown by more basic peptides. The CEC separation of these peptides with the Hypersil n-…

chemistry.chemical_classificationCapillary electrochromatographySorbentChromatographyResolution (mass spectrometry)Salt (chemistry)Context (language use)ElectrolyteBiochemistrychemistry.chemical_compoundElectrophoresisEndocrinologychemistryAcetonitrileThe Journal of Peptide Research
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Ionic transport characteristics of negatively and positively charged conical nanopores in 1:1, 2:1, 3:1, 2:2, 1:2, and 1:3 electrolytes

2019

We study experimentally the current (I)-voltage (V) curves of 1:1, 2:1, 3:1, 2:2, 1:2, and 1:3 electrolytes in positively and negatively charged conically-shaped pores of nanoscale dimensions. The positive charges are poly(allylamine hydrochloride) chains functionalized on the pore surface by electrostatic interactions while the negative charges are carboxylic acid groups. Under physiological conditions, these fixed-charge groups are ionized and strongly interact with the different monovalent, divalent, and trivalent ions in the pore solution. The current rectification of the I-V curves and the membrane potentials provide fundamental information on the interaction of the pore charge groups …

chemistry.chemical_classificationCarboxylic acidIonic bonding02 engineering and technologyElectrolyte010402 general chemistry021001 nanoscience & nanotechnologyElectrostatics01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDivalentIonBiomaterialsNanoporeColloid and Surface ChemistrychemistryChemical physics0210 nano-technologyTransport phenomenaJournal of Colloid and Interface Science
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Chemical speciation of organic matter in natural waters. Interaction of nucleotide 5′ mono-, di- and triphosphates with major components of seawater

2004

AbstractThe interactions of nucleotide 5’ mono-, di- and triphosphates in a multicomponent ionic medium simulating the macro-composition of seawater (Na+, K+, Ca2+, Mg2+, Cl-, SO42-, Synthetic Sea Water, SSW) have been investigated at different ionic strengths and at T= 25°C. A chemical speciation model, according to which all the internal interactions between the components of the ionic medium are taken into account, was applied to determine the effective formation constants of species in the nucleotide-seawater system. The results were compared to protonation parameters calculated from single electrolyte systems. A simpler model (SSW considered as a single salt BA, with Bz+ and Az-), repr…

chemistry.chemical_classificationChemical Health and SafetyHealth Toxicology and MutagenesisInorganic chemistrySalt (chemistry)Ionic bondingProtonationElectrolytenucleotideToxicologyorganic natural matterIonspeciationchemistryStability constants of complexesspeciation; nucleotide; seawater; organic natural matterQualitative inorganic analysisSeawaterChemical speciation of organic matter. Complex formation. Natural waters. Nucleotidesseawater
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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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Clickable poly-L-lysine for the formation of biorecognition surfaces

2019

Biomolecules are immobilized onto surfaces employing the fast and stable adsorption of poly-l-lysine (PLL) polymers and the versatile copper-free click chemistry reactions. This method provides the combined advantages of versatile surface adsorption with density control using polyelectrolytes and of the covalent and orthogonal immobilization of biomolecules with higher reaction rates and improved yields of click chemistry. Using DNA attachment as a proof of concept, control over the DNA probe density and applicability in electrochemical detection are presented.

chemistry.chemical_classificationChemistryGeneral Chemical EngineeringBiomoleculeLysineADN02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryPolyelectrolyte0104 chemical sciencesReaction rateAdsorptionBiomolèculesCovalent bondClick chemistry0210 nano-technology
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Coil overlap in moderately concentrated polyelectrolyte solutions: effects of self-shielding as compared with salt-shielding as a function of chain l…

2016

The generalized intrinsic viscosity {η} (hydrodynamic volume of the solute at arbitrary polymer concentration c) – introduced by analogy to the intrinsic viscosity [η] – provides access to the degree of coil overlap Ω for polyelectrolyte solutions in pure water or in saline water. The experimental basis of this investigation consists in viscosity measurements as a function of c for a large number of sodium polystyrene sulfonate (Na-PSS) samples covering the molecular weight range from 0.91 to 1000 kg mol−1. The accurate modeling of these dependencies with a maximum of three parameters yields detailed information on Ω as a function of (c[η]) in the absence and in the presence of extra salt. …

chemistry.chemical_classificationChemistryGeneral Chemical EngineeringIntrinsic viscosityThermodynamics02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPolyelectrolyte0104 chemical sciencesDilutionViscosityElectromagnetic shielding0210 nano-technologySodium Polystyrene SulfonateConstant (mathematics)RSC Advances
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Buildup of ultrathin multilayer films by a self-assembly process: III. Consecutively alternating adsorption of anionic and cationic polyelectrolytes …

1992

A solid substrate with a positively charged planar surface is immersed in a solution containing an anionic polyelectrolyte and a monolayer of the polyanion is adsorbed. Since the adsorption is carried out at relatively high concentrations of polyelectrolyte, a large number of ionic residues remain exposed to the interface with the solution and thus the surface charge is effectively reversed. After rinsing in pure water the substrate is immersed in the solution containing a cationic polyelectrolyte. Again a monolayer is adsorbed but now the original surface charge is restored. By repeating both steps in a cyclic fashion, alternating multilayer assemblies of both polymers are obtained. The bu…

chemistry.chemical_classificationChemistrySmall-angle X-ray scatteringMetals and AlloysCationic polymerizationAnalytical chemistrySurfaces and InterfacesPolymerPolyelectrolyteSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdsorptionChemical engineeringMonolayerMaterials ChemistrySelf-assemblySurface chargeThin Solid Films
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Electrochemical technology for the treatment of real washing machine effluent at pre-pilot plant scale by using active and non-active anodes

2018

Abstract Real effluent of washing machine is one of the major sources of microplastics and fabrics in municipal and surface water. The effluents constitute large volume of wastewater with different surfactants since every household and industries nowadays use washing machine rather than traditional hand washing. In this work, a real effluent of washing machine was treated by electrooxidation (EO) in a pre-pilot plant scale electrochemical flow reactor using active (Ti/Pt) or non-active (boron doped diamond (BDD)) anodes and Ti cathode. The effect of anode material (Ti/Pt or BDD) and the applied current density (16.6, 33.3 and 66.6 mA cm−2) on the decay of the organic matter, in terms of che…

chemistry.chemical_classificationChemistrySupporting electrolyteGeneral Chemical EngineeringChemical oxygen demand02 engineering and technology010501 environmental sciences021001 nanoscience & nanotechnologyPulp and paper industry01 natural sciencesCathodeAnalytical ChemistryAnodelaw.inventionPilot plantWastewaterlawElectrochemistryOrganic matter0210 nano-technologyEffluent0105 earth and related environmental sciencesJournal of Electroanalytical Chemistry
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Electrochemical synthesis of sulfamides.

2021

Herein we demonstrate the first electrochemical synthesis protocol of symmetrical sulfamides directly from anilines and SO2 mediated by iodide. Sulfamides are an emerging functional group in drug design. Highlights are the direct use of SO2 from a stock solution and no necessity of any supporting electrolyte. Overall, the reaction has been demonstrated for 15 examples with yields up to 93%.

chemistry.chemical_classificationChemistrySupporting electrolyteIodideMetals and AlloysGeneral ChemistryElectrochemistrycomplex mixturesCombinatorial chemistryCatalysisrespiratory tract diseasesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundFunctional groupMaterials ChemistryCeramics and CompositesStock solutionChemical communications (Cambridge, England)
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Solution properties of polyelectrolytes

1991

Abstract Chromatographic data for sodium polystyrene sulphonate were obtained on both silica- and polymer-based size-exclusion supports using mobile phases of various pH and ionic strength. Deviations of the elution volume were observed towards both lower and higher values relative to the reference calibration graph obtained with uncharged standards. An empirical correlation is proposed in order to account for all the secondary effects observed. The general applicability of this correlation was further tested for chromatographic data obtained for a series of peptides and proteins on a silica-based support under very different eluent conditions. Deviations from ideal elution behaviour such a…

chemistry.chemical_classificationChromatographyAqueous solutionCalibration curveChemistryElutionSodiumSize-exclusion chromatographyOrganic ChemistryInorganic chemistryAnalytical chemistrychemistry.chemical_elementGeneral MedicinePolymerBiochemistryPolyelectrolyteAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyIonic strengthSodium nitratePhase (matter)Ideal (ring theory)Sodium polystyrene sulphonateJournal of Chromatography A
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