Search results for "ionic strength"

showing 10 items of 198 documents

Modeling the sorption of Np(V) on Na-montmorillonite – effects of pH, ionic strength and CO2

2019

Abstract Results from batch type experiments were modeled using the 2 SPNE SC/CE model developed by Bradbury and Baeyens. This work focused on the applicability of this model to the sorption of Np(V) on Na-montmorillonite under high saline conditions (0.1–3.0 M NaCl) in the pH range of 2–10 and in the presence of dissolved CO2 (p(CO2) = 10−3.3 atm). Under ambient air conditions two additional surface complexation species had to be taken into account, which are ternary species involving one carbonate ligand (≡SONpO2(CO3)2−, ≡SONpO2(CO3)Na−). The gained set of complexation parameters was successfully tested over a wide range of Np(V) concentrations (10−4 to 10−12 M) under Ar atmosphere and am…

NeptuniumInorganic chemistrychemistry.chemical_elementSorption010501 environmental sciences010403 inorganic & nuclear chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundMontmorillonitechemistryIonic strengthPhysical and Theoretical Chemistry0105 earth and related environmental sciencesRadiochimica Acta
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Direct measurement of the melting temperature of supported DNA by electrochemical method

2003

The development of biosensors based on DNA hybridization requires a more precise knowledge of the thermodynamics of the hybridization at a solid interface. In particular, the selectivity of hybridization can be affected by a lot of parameters such as the single-strand (ss)DNA density, the pH, the ionic strength or the temperature. The melting temperature, T(m), is in part a function of the ionic strength and of the temperature and therefore provides a useful variable in the control of the selectivity and sensitivity of a DNA chip. The electrochemical technique has been used to determine the T(m) values when the probe is tethered by a DNA self-assembled monolayer (SAM). We have built a speci…

Osmolar ConcentrationTemperatureAnalytical chemistryDNABiologyNucleic Acid DenaturationElectrochemistrySensitivity and SpecificityMolecular biologyRedox indicatorIonic strengthMonolayerElectrodeElectrochemistryGeneticsThermodynamicsA-DNASelectivityElectrodesOxidation-ReductionBiosensorNAR Methods OnlineOligonucleotide Array Sequence AnalysisNucleic Acids Research
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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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Solution Properties of Poly-Electrolytes. XI. Adsorption Effects in Aqueous Size-Exclusion Chromatog-Raphy of Polyanions

1994

Abstract Elution profiles of a series of polymer standards such as sodium poly(styrene sulphonate), poly(acrylic acid) and poly(L-glutamic acid) have been obtained from size-exclusion chromatography experiments using separately two types of hydrophilic supports. A variety of mobile phase compositions have been performed to enhance adsorption effects in order to study how this phenomenon can affect to the chromatographic separation mechanism of polyanions. Distribution coefficient values, in general greater than unity, have served to quantify the adsorption effect, as well as to analyze their dependence on eluent ionic strength, on the ionic groups of the support and on the chemical nature a…

Partition coefficientAqueous solutionAdsorptionChromatographyMolar massChemistryIonic strengthElutionSize-exclusion chromatographyMolecular MedicineIonic bondingJournal of Liquid Chromatography
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Influence of temperature and background electrolyte on the sorption of neptunium(V) on Opalinus Clay

2012

Abstract The temperature dependence of the sorption of 8 μM neptunium(V) on Opalinus Clay (OPA, Mont Terri, Switzerland) was investigated between 40 and 80 °C and compared to previous results for 20 °C. The batch experiments were performed under ambient air conditions in synthetic pore water (pH = 7.6, I = 0.4 M) under variation of the solid-to-liquid ratio between 2 and 20 g/L. Under these conditions the sorption of Np(V) on OPA was found to be an endothermic process as the average distribution coefficient (K d ) increases continuously with increasing temperature from 23 ± 4 L/kg at 40 °C to 678 ± 254 L/kg at 80 °C. In the temperature range of 40-80 °C, the plot of log(K d ) vs. 1/T could …

Partition coefficientGeochemistry and PetrologyIonic strengthChemistryMagnesiumNeptuniumEnthalpychemistry.chemical_elementGeologySorptionElectrolyteAtmospheric temperature rangeNuclear chemistryApplied Clay Science
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Macromolecules in ordered media III. A fluorescence study on the association of poly-2-vinylpyridine with a phospholipid bilayer

2007

Association of low molecular weight poly-2-vinylpyridine taken as a polycation model with unilamellar vesicles based on dimirystoylphosphatidic acid has been experimentally investigated by means of fluorescence energy transfer experiments. The conventional profiles for the binding isotherms were obtained, confirming strong deviations from the ideality of these complex fluid composites. Two approaches, named binding and partitioning equilibrium, respectively, were used to obtain the association constant, K A; the number of phospholipids that form a binding site, N; the partition coefficient, Λ; the activity coefficient, γ; and the effective charge, v. Analysis of these parameters as a functi…

Partition coefficientchemistry.chemical_classificationActivity coefficientChemistryIonic strengthVesicleAnalytical chemistryPhysical chemistryPolymerLipid bilayerEffective nuclear chargeMacromolecule
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Complex formation of Tb3+ with glycolate, D-gluconate and α-isosaccharinate in neutral aqueous perchlorate solutions

2003

Summary An electromigration technique was used for measurements of metal-ligand formation constants of non-carrier-free 160Tb3+ with glycolate, D-gluconate and α-isosaccharinate ligands. The overall ion mobilities of Tb at different concentrations of the ligands were measured in chemically inert perchlorate solutions (pH 7 and T= 298.1K) with an overall ionic strength μ = 0.1. The stepwise stoichiometric stability constants are: Tb3+/glycolate: log K 1=2.72(18), log K 2=1.73(19), log K 3= 1.12(17), Tb3+/D-gluconate: log K 1=2.96(11), log K 2=2.60(11), log K 3=1.13(9), Tb3+/α-ISA: log K 1=3.07(8), log K 2 = 2.69(11), log K 3 = 1.80(12).

Perchloratechemistry.chemical_compoundAqueous solutionchemistryD-gluconateIonic strengthStability constants of complexesStereochemistryComplex formationPhysical chemistryPhysical and Theoretical ChemistryStoichiometryIonRadiochimica Acta
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The Electrostatic Expansion of Linear Polyelectrolytes:  Effects of Gegenions, Co-ions, and Hydrophobicity

1997

The molar mass and ionic strength dependence of the dimensions of hydrophobically modified poly(vinylpyridinium) cations are demonstrated to be almost perfectly described by a theoretical expression derived on the basis of only excluded volume considerations. Generally, the effective charge density of the polyions decreases significantly with increasing hydrophobicity and with increasing polarizability of the gegenions. Unexpectedly, the intrinsic excluded volume effect which becomes dominating at high ionic strength not only depends on the hydrophobicity of the polyion but also significantly increases with decreasing polarizability of the gegenions (i.e., if the iodide gegenions are replac…

Persistence lengthchemistry.chemical_classificationMolar massPolymers and PlasticsChemistryOrganic ChemistryEffective nuclear chargePolyelectrolyteInorganic ChemistryIonic strengthPolarizabilityChemical physicsExcluded volumePolymer chemistryMaterials ChemistryCounterionMacromolecules
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QRAR models for central nervous system drugs using biopartitioning micellar chromatography.

2002

The capability of biopartitioning Micellar Chromatography, BMC, to describe and estimate pharmacokinetic and pharmacodynamic parameters of central nervous system drugs is reviewed in this article. BMC is a mode of micellar liquid chromatography, MLC, that uses micellar mobile phases of Brij35 (polyoxyethilene(23) lauryl ether) prepared in physiological conditions (pH, ionic strength). The retention of a drug in this system depends on its hydrophobic, electronic and steric properties, which also determine its biological activity. The results of BMC studies suggest that this in vitro approach is an attractive useful tool to be implemented into the lead optimization step of drug development sc…

PharmacologyDrugChromatographyChemistrymedia_common.quotation_subjecttechnology industry and agricultureQuantitative Structure-Activity Relationshipmacromolecular substancesGeneral Medicinemusculoskeletal systemModels BiologicalPharmacokineticsDrug developmentIonic strengthMicellar liquid chromatographyDrug DiscoveryAnimalsHumansmedia_commonCentral Nervous System AgentsChromatography Micellar Electrokinetic CapillaryMini reviews in medicinal chemistry
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Unravelling the modus operandi of phytosiderophores during zinc uptake in rice: the importance of geochemical gradients and accurate stability consta…

2020

Abstract Micronutrient deficiencies threaten global food production. Attempts to biofortify crops rely on a clear understanding of micronutrient uptake processes. Zinc deficiency in rice is a serious problem. One of the pathways proposed for the transfer of zinc from soils into rice plants involves deoxymugineic acid (DMA), a phytosiderophore. The idea that phytosiderophores play a wider role in nutrition of Poaceae beyond iron is well established. However, key mechanistic details of the DMA-assisted zinc uptake pathway in rice remain uncertain. In particular, questions surround the form in which zinc from DMA is taken up [i.e. as free aqueous Zn(II) or as Zn(II)–DMA complexes] and the role…

PhysiologyIronmedia_common.quotation_subjectPlant Biology & Botany0607 Plant Biology0703 Crop and Pasture Productionchemistry.chemical_elementPlant ScienceZincrice (Oryza sativa)010501 environmental sciencesDeoxymugineic acid01 natural sciencesgeochemical gradientsSoilZinc deficiency (plant disorder)phytosiderophore0105 earth and related environmental sciencesmedia_commonRhizosphere0604 GeneticsChemistryLigandzinc uptakeBiological TransportOryza04 agricultural and veterinary sciencesMicronutrientmicroenvironmentstability constantsZincSpeciationIonic strengthEnvironmental chemistry040103 agronomy & agriculture0401 agriculture forestry and fisheriesZinc uptakerhizosphere
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