Search results for "aqueous solution"

showing 10 items of 1610 documents

The influence of ultrasound on the RuI3-catalyzed oxidation of phenol: Catalyst study and experimental design

2009

Abstract The influence of ultrasound at 24 kHz on the heterogeneous aqueous oxidation of phenol over RuI3 with hydrogen peroxide (H2O2) was studied isothermally at 298 K. Effect of ultrasound irradiation on catalytic properties and performance of RuI3 has been studied in details by means of scanning electron microscopy (SEM), X-ray powder diffraction (XRD), dispersion analyzer and a surface analyzer. Turn over frequency of the catalyst was also calculated. In this work, experimental design methodology was applied to optimize the degradation of phenol in aqueous solution, while minimizing an excessive consumption of chemical reagents. The independent variables considered were the catalyst lo…

Aqueous solutionStereochemistryChemistryProcess Chemistry and TechnologyInorganic chemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundCatalytic oxidationReagentPhenolLeaching (metallurgy)Hydrogen peroxideGeneral Environmental ScienceApplied Catalysis B: Environmental
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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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Ellipsometric and fluorescence microscopic investigations of a cyclam derivative at the air/water interface

1993

Aqueous solutionStereochemistrySurfaces and InterfacesCondensed Matter PhysicsSurface pressureFluorescencechemistry.chemical_compoundchemistryEllipsometryCyclamMonolayerElectrochemistryFluorescence microscopePhysical chemistryGeneral Materials ScienceSpectroscopyDerivative (chemistry)Langmuir
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Influence of chloride anions on the electrodeposition and electroactivity of the polymer matrix in polypyrrole, poly( N -methylpyrrole) and polypyrro…

2004

We report electrochemical studies on the influence of a small concentration of chloride ions on the electroactivity of the polymer matrix of polypyrrole (PPy), poly(N-methylpyrrole) [p(N-MePy)] and a poly(titanocene-propyl-pyrrole) derivative, p(Tc3Py) [Tc(CH2)3NC4H4; Tc=CpCp′TiCl2; Cp=C5H5; Cp′=C5H4] in acetonitrile (AN), tetrahydrofuran (THF) and N,N-dimethylformamide (DMF). The polymer films were obtained on Pt disc electrodes from AN solutions of the monomers containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF6) as the supporting electrolyte and then transferred to the corresponding monomer-free solution. Studies in Cl−-containing solutions have shown that the p(Tc3Py) matrix…

Aqueous solutionSupporting electrolyteInorganic chemistryCondensed Matter PhysicsElectrochemistryPolypyrroleChloridechemistry.chemical_compoundMonomerchemistryTetrabutylammonium hexafluorophosphatePolymer chemistryElectrochemistrymedicineGeneral Materials ScienceElectrical and Electronic EngineeringAcetonitrilemedicine.drugJournal of Solid State Electrochemistry
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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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Removal of drugs in aqueous systens by photoassisted degradation

2005

Aqueous solutions of tetracycline, lincomycin and ranitidine were irradiated with UV light in homogeneous and heterogeneous systems. Two commercial polycrystalline TiO2 powders (Degussa P25 and Merck) were used as photocatalysts. After 5A h, an appreciable photolytic degradation of tetracycline and ranitidine was observed while the degradation of lincomycin was noticeably lower. As far as the mineralization is concerned, a small decrease of the TOC values was measured in the case of tetracycline whereas negligible variations were found for lincomycin or ranitidine. The presence of the photocatalysts greatly enhanced the degradation rates of the drugs with respect to those observed during th…

Aqueous solutionTetracyclineGeneral Chemical EngineeringInorganic chemistryLincomycinchemistry.chemical_compoundAdsorptionchemistryAntibioticsveterinary antibioticsTitanium dioxideMaterials ChemistryElectrochemistryPhotocatalysismedicineSettore CHIM/07 - Fondamenti Chimici Delle TecnologieoxytetracyclinePhotodegradationmedicine.drugAntibacterial agent
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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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