Search results for "analytical"

showing 10 items of 9586 documents

Dependence of the mobility of tracer ions in aqueous perchlorate solutions on the hydrogen ion concentration

2003

The dependence of the absolute individual ion mobility (AIIM) of the carrier-free radioactive ions [137Cs]Cs+, [201Tl]Tl+ and [57Co]Co2+ on the hydrogen ion concentration in aqueous perchlorate electrolyte mixtures was studied by means of the electromigration technique. The AIIM of the radioactive ions was found to decrease as the hydrogen ion concentration of the electrolyte mixture increases. Above pH > 4 there is a fairly good agreement between experimental and calculated values. Below pH 4 the experimentally observed decrease of the AIIM is not explained by the extended Debye–Huckel–Onsager limiting law. The effect can possibly be explained by a change of the dynamical properties of ele…

Aqueous solutionProtonHydroniumInorganic chemistryAnalytical chemistryGeneral Physics and AstronomyElectrolyteIonPerchloratechemistry.chemical_compoundReaction rate constantchemistryMoleculePhysical and Theoretical ChemistryPhys. Chem. Chem. Phys.
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Protonation of Carbonate in Aqueous Tetraalkylammonium Salts at 25°C.

2006

Protonation constants of carbonate were determined in tetramethylammonium chloride (Me4NClaq 0.1≤I/mol kg−1 ≤4) and tetraethylammonium iodide (Et4NIaq 0.1≤I/mol kg−1 ≤1) by potentiometric ([H+]-glass electrode) measurements. Dependence of protonation constants on ionic strength was taken into account by modified specific ion interaction theory (SIT) and by Pitzer models. Literature data on the protonation of carbonate in NaClaq (0.1≤I/mol kg−1 ≤6) were also critically analysed. Both protonation constants of carbonate follow the trend Et4NI>Me4NCl > NaCl. An ion pair formation model designed to take into account the different protonation behaviours of carbonate in different supporting electr…

Aqueous solutionProtonation of carbonateSpecific ion interaction theory (SIT)Ion pair formation modelChemistryInorganic chemistryTetraalkylammonium saltProtonationDependence on ionic strengthElectrolyteIon pairsAnalytical Chemistrychemistry.chemical_compoundIonic strengthTetramethylammonium chlorideAqueous solutionPitzer equationsCarbonateSettore CHIM/01 - Chimica AnaliticaProtonation of carbonate; Dependence on ionic strength; Aqueous solution; Tetraalkylammonium salts; Ion pair formation model; Specific ion interaction theory (SIT); Pitzer equationPitzer equation
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Design, Synthesis and Evaluation of Enzyme-Responsive Fluorogenic Probes Based on Pyridine-Flanked Diketopyrrolopyrrole Dyes

2020

The ever-growing demand for fluorogenic dyes usable in the rapid construction of analyte-responsive fluorescent probes, has recently contributed to a revival of interest in the chemistry of diketopyrrolopyrrole (DPP) pigments. In this context, we have explored the potential of symmetrical and unsymmetrical DPP derivatives bearing two or one 4-pyridyl substituents acting as optically tunable group(s). The unique fluorogenic behavior of these molecules, closely linked to N-substitution/charge state of their pyridine unit (i.e., neutral pyridine or cationic pyridinium), has been used to design DPP-based fluorescent probes for detection of hypoxia-related redox enzymes and penicillin G acylase …

Aqueous solutionPyridinesCationic polymerizationContext (language use)02 engineering and technologyKetones010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFluorescenceCombinatorial chemistryAtomic and Molecular Physics and Optics0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryPyridineMoleculePyrrolesPyridinium0210 nano-technologyInstrumentationBiosensorSpectroscopyFluorescent Dyes
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Composite Thin Film by Hydrogen-Bonding Assembly of Polymer Brush and Poly(vinylpyrrolidone)

2005

Based on hydrogen-bonding layer-by-layer (LBL) assembly in aqueous solution, poly(vinylpyrrolidone) (PVPON) and a spherical polymer brush with a poly(methylsilsesquioxane) (PSQ) core and poly(acrylic acid) (PAA) hair chains were used to fabricate composite multilayer thin films. Hydrogen bonding as the driving force was confirmed by FT-IR spectrometry. A simple method (Filmetric F20) was introduced to determine the thickness and refractive index of the films. The film thickness was found to be a linear function of the number of bilayers. The average increase in thickness per bilayer is 28.3 nm. The film morphology was characterized with scanning electron microscopy and atomic force microsco…

Aqueous solutionScanning electron microscopeBilayerComposite numberAnalytical chemistrySurfaces and InterfacesCondensed Matter PhysicsPolymer brushchemistry.chemical_compoundchemistryChemical engineeringElectrochemistryGeneral Materials ScienceThin filmRefractive indexSpectroscopyAcrylic acidLangmuir
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Conformational investigations of bis(α-aminoalkyl)phosphinic acids and studies of the stability of their complexes with Cu(II)

2008

Abstract Conformational investigations of a group of bis(α-aminoalkyl)phosphinic acids were performed by use of NMR spectroscopy and theoretical calculations. In the case of one of the studied compounds, substituted with aminobenzyl and amino(p-chlorobenzyl) moieties, a pH-dependent equilibrium between conformers, stabilized by intermolecular hydrogen bonds was observed. Potentiometric studies proved that these molecules formed stable complexes with copper(II) ions, where stoichiometry was 1:1 and 1:2 depending on pH of their aqueous solution.

Aqueous solutionStereochemistryHydrogen bondChemistryOrganic ChemistryIntermolecular forcePotentiometric titrationNuclear magnetic resonance spectroscopyAnalytical ChemistryInorganic ChemistryPolymer chemistryMoleculeConformational isomerismSpectroscopyStoichiometryJournal of Molecular Structure
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Uranium(VI) sequestration by polyacrylic and fulvic acids in aqueous solution

2011

Stability data on the formation of dioxouranium(VI) species with polyacrylic (PAA) and fulvic acids (FA) are reported with the aim to define quantitatively the sequestering capacity of these high molecular weight synthetic and naturally occurring ligands toward uranium(VI), in aqueous solution. Investigations were carried out at t = 25 °C in NaCl medium at different ionic strengths and in absence of supporting electrolyte for uranyl–fulvate (\( {{\text{UO}}_{2}}^{2+} \)–FA) and uranyl–polyacrylate (\( {{\text{UO}}_{ 2}}^{ 2+ } \)–PAA, PAA MW 2 kDa) systems, respectively. The experimental data are consistent with the following speciation models for the two systems investigated: (i) UO2(FA1),…

Aqueous solutionSupporting electrolyteLigandHealth Toxicology and MutagenesisDioxouranium(VI) cation Uranium sequestration Uranyl–polycarboxylate interactions Fulvic acid Polyacrylic acid Metal complexes in aqueous solutionPolyacrylic acidPublic Health Environmental and Occupational Healthchemistry.chemical_elementIonic bondingUraniumUranylPollutionAnalytical ChemistryIonchemistry.chemical_compoundNuclear Energy and EngineeringchemistryPhysical chemistryRadiology Nuclear Medicine and imagingSettore CHIM/01 - Chimica AnaliticaSpectroscopyNuclear chemistry
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Thermal and Chemical Stability of Thiol Bonding on Gold Nanostars

2015

The stability of thiol bonding on the surface of star-shaped gold nanoparticles was studied as a function of temperature in water and in a set of biologically relevant conditions. The stability was evaluated by monitoring the release of a model fluorescent dye, Bodipy-thiol (BDP-SH), from gold nanostars (GNSs) cocoated with poly(ethylene glycol) thiol (PEG-SH). The increase in the BDP-SH fluorescence emission, quenched when bound to the GNSs, was exploited to this purpose. A maximum 15% dye release in aqueous solution was found when the bulk temperature of gold nanostars solutions was increased to T = 42 °C, the maximum physiological temperature. This fraction reduces 3-5% for temperatures …

Aqueous solutionSurface PropertiesAnalytical chemistryMetal NanoparticlesCondensed Matter PhysicSurfaces and InterfacesCondensed Matter PhysicsElectrochemistryPhotochemistryFluorescenceNanostructureschemistry.chemical_compoundchemistryColloidal goldElectrochemistryGeneral Materials ScienceChemical stabilityThermal stabilityGoldSulfhydryl CompoundsMaterials Science (all)Surface plasmon resonanceSurfaces and InterfaceEthylene glycolSpectroscopyLangmuir
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Protein aggregation induced by phase separation in a pea proteins–sodium alginate–water ternary system

2012

Abstract The physicochemical properties of a native, globular plant protein–linear anionic polysaccharide aqueous system at 20 °C were investigated in conditions where biopolymers carry a net negative charge (pH 7.2, 0.1 M NaCl). The pea proteins–sodium alginate mixtures showed a phase separation mainly by thermodynamic incompatibility, characterized at both the macroscopic and microscopic scale. Phase diagram was established and confocal laser scanning microscopy (CLSM) provided accurate data on the microstructure morphology of the system, regarding its phase behavior. In admixture, sodium alginate induced a protein aggregation, certainly by a local depletion of the polysaccharide. Protein…

Aqueous solutionTernary numeral systemChemistryGeneral Chemical EngineeringPea proteinAnalytical chemistryGeneral ChemistryProtein aggregationengineering.materialChemical engineeringPhase (matter)Volume fractionengineeringBiopolymerPhase inversionFood ScienceFood Hydrocolloids
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Thermodynamic properties of water-β-cyclodextrin-dodecylsurfactant ternary systems

1995

Densities, heat capacities and conductivities of water-surfactant-β-cyclodextrin (β-CD) ternary systems were determined at 25°C. The surfactants studied were sodium dodecylsulfate (NaDS) and dodecyltrimethylammonium bromide (DTAB). From conductivity data, apparent critical micelle concentrations (cmc*) and degree of ionization of micelles were obtained at a fixed β-CD concentration (mCD). From the cmc* value and that in water (cmc) the stoichiometry of the surfactant-β-CD complex was calculated. At a given mCD, the apparent molar volume Vϕ,CD and heat capacity Cϕ,CD of β-CD in the two surfactants were calculated as functions of surfactant concentration mS. For both NaDS and DTAB, Vϕ,CD incr…

Aqueous solutionTernary numeral systemChemistryInorganic chemistryBiophysicsAnalytical chemistryBiochemistryMicelleHeat capacityDegree of ionizationMolar volumePulmonary surfactantCritical micelle concentrationPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Synthesis, characterization and thermal behavior of nine new -type quaternary ammonium tetrafluoroborate or hexafluorophosphate salts prepared by met…

2008

Abstract Nine new quaternary ammonium tetrafluoroborate or hexafluoroborate salts were prepared from analogous bromide or chloride salts using anion exchange reaction in which the corresponding bromide or chloride salt was treated with HBF4 or HPF6 acid in aqueous solutions. The characterizations were performed by 1H NMR and 13C NMR spectroscopy as well as by elemental analysis. The single crystals of three tetrafluoroborate and two hexafluorophosphate salts were obtained by slow evaporation from a methanol/ethyl acetate solution and the crystal structures were determined by X-ray single crystal diffraction. Four of the compounds crystallized in the orthorhombic and one in the monoclinic cr…

Aqueous solutionTetrafluoroborateOrganic ChemistryInorganic chemistryHalideCrystal structureChlorideAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryBromideHexafluorophosphatemedicineSpectroscopymedicine.drugMonoclinic crystal systemJournal of Molecular Structure
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