Search results for "aqueous solution"

showing 10 items of 1610 documents

Complexation of the potassium ion by diaza crown compounds in aqueous solutions

1988

The conductance behavior of potassium nitrate in water with and without 1,7,10,16-tetraoxa-4,13-diazacyclooctandecane[2.2] and 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo-8.8.8-exacosane[2.2.2] macrocyclic ligands have been studied in order to analyze the complexation behavior of potassium cations in water. The absence of the complexation found in the [2.2] system is discussed in terms of the ligand structural features (presence of hydrogen bond donor and acceptor sites). The ion pair association constant of potassium cryptate as obtained from conductance measurements is also reported and discussed.

Aqueous solutionChemistryLigandHydrogen bondPotassiumInorganic chemistryBiophysicsConductancechemistry.chemical_elementPotassium nitrateBiochemistryCrown Compoundschemistry.chemical_compoundStability constants of complexesPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Lateral organization of G M1 in phase-separated monolayers visualized by scanning force microscopy

2002

Phase separation of glycolipids in lipid mono- and bilayers is of great interest for the understanding of membrane function. The distribution of the ganglioside GM1 in sphingomyelin (SM)/1-palmitoyl-2-oleoyl- sn-glycero-3-phosphocholine (POPC), SM/1,2-dipalmitoyl- sn-glycero-3-phosphocholine (DOPC) and SM/cholesterol/POPC Langmuir-Blodgett (LB) monolayers transferred at 36 mN/m has been studied by scanning force microscopy. Besides lateral organization of the glycolipid in LB monolayers as deduced from topography, material properties have been investigated by phase imaging, pulsed force mode and force modulation microscopy. It was shown that GM1 preferentially clusters in an ordered lipid m…

Aqueous solutionChemistryLipid BilayersBiophysicsAnalytical chemistryBrainMembranes ArtificialG(M1) GangliosideGeneral MedicineMicroscopy Atomic ForceLipidsMicelleSphingomyelinschemistry.chemical_compoundCrystallographyCholesterolGlycolipidPhase (matter)MicroscopyMonolayerPhosphatidylcholinesSphingomyelinPOPCEuropean Biophysics Journal
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Calculation of the pH and the titratable acidity in clinically used infusion solutions.

2006

Clinically used infusion solutions are complex aqueous mixtures composed of a variety of different salts, acids, and non-electrolytes, and are characterized by composition, initial pH, and titratable acidity (TA). By rigorous treatment as a multi-composed acid-base system, pH and TA were calculated from proton dissociation equilibria, mass balance equations and electroneutrality condition. Nine were arbitrarily chosen as model solutions in which pH and TA were experimentally determined. From composition, and based on a set of apparent acidity constants (pK values) at 37 degrees C and total ionic strength 0.155 mol/l, pH was calculated by iteration. In the model solutions, measured pH was in…

Aqueous solutionChemistryMass balanceProton dissociationAnalytical chemistryTitrimetryHealth InformaticsTitratable acidHydrogen-Ion ConcentrationMean differenceComputer Science ApplicationsBody FluidsFluid therapyModels ChemicalIonic strengthBiomimetic MaterialsFluid TherapyComposition (visual arts)Computer SimulationInfusions ParenteralInfusions IntravenousSoftwareComputer methods and programs in biomedicine
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Mößbauer- und ESCA-Untersuchungen zur Bildung oxidischer Eisenphasen in wäßrigen Medien unter der Einwirkung organischer Korrosionsinhibitoren

1982

Korrosionsschichten auf Stahl nach Exposition in Wasser mit bestimmter Harte und Chloridgehalt wurden hinsichtlich der Wirksamkeit beigefugter organischer Inhibitoren mittels Mosbauer- und ESCA-Spektroskopie untersucht. Es entstehen relativ dicke Schichten mit einem unerwartet niedrigen Eisengehalt in Form von FeOOH. Die Schichten enthalten merkliche Mengen von Ionen aus der Testlosung und auch Abbauprodukte der Inhibitormolekule. Letztere werden anscheinend in dem korrosiven Medium zersetzt. Es ist anzunehmen, das das Gesamtmolekul zwar den Transport des Inhibitors zum Metall beeinflust, die eigentliche Inhibierung aber allein durch funktionelle Gruppen erfolgt. Mossbauer and ESCA investig…

Aqueous solutionChemistryMechanical EngineeringMetals and AlloysGeneral MedicineChlorideSurfaces Coatings and FilmsMechanics of MaterialsIron metalPolymer chemistryIron contentMössbauer spectroscopyMaterials ChemistrymedicineEnvironmental Chemistrymedicine.drugMaterials and Corrosion
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A biocompatible ZnNa2-based metal–organic framework with high ibuprofen, nitric oxide and metal uptake capacity

2020

Metal organic frameworks (MOFs) have received significant attention in recent years in the areas of biomedical and environmental applications. Among them, mixed metal MOFs, although promising, are relatively few in number in comparison with their homometallic analogues. The employment of benzophenone-4,4′-dicarboxylic acid (bphdcH2) in mixed metal MOF chemistry provided access to a 3D MOF, [Na2Zn(bphdc)2(DMF)2]n (NUIG1). NUIG1 displays a new topology and is a rare example of a mixed metal MOF based on 1D rod secondary building units. UV-vis, HPLC, TGA, XRPD, solid state NMR and computational studies indicated that NUIG1 exhibits an exceptionally high Ibuprofen (Ibu) and nitric oxide adsorpt…

Aqueous solutionChemistryMetal ions in aqueous solutionInorganic chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMagnetic susceptibility0104 chemical sciencesMetalAdsorptionSolid-state nuclear magnetic resonanceChemistry (miscellaneous)visual_artvisual_art.visual_art_mediumGeneral Materials ScienceMetal-organic framework0210 nano-technologyPowder diffractionMaterials Advances
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Synthesis and characterization of acetazolamide complexes of Ni(II), Cd(II), Hg(II), and Ag(I)

1989

The preparation and characterization of K2Ni2(Acm)3·5H2O, Cd(Acm)·32 H2O, Hg(Acm)·12H2O, Ag2(Acm), and Ag2(Acm)(NH3) complexes are described. The spectral properties suggest that Acm interacts with the metal ions through the doubly deprotonated form as observed in the [Cu(Acm)(NH3)2(OH2)]2·2H2O complex, whose crystalline structure has been previously reported. The crystal field parameters of the Ni(II) complex indicate an octahedral environment for the metal ion in the solid and its aqueous, DMSO, and DMF solutions. UV spectra of all the Acm complexes until now synthesized are discussed.

Aqueous solutionChemistryMetal ions in aqueous solutionSpectral propertiesAnalytical chemistryCrystal structureBiochemistryInorganic ChemistryCrystalMetalCrystallographyDeprotonationOctahedronvisual_artvisual_art.visual_art_mediumJournal of Inorganic Biochemistry
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Electrochemical molecular recognition of silver cation by electropolymerised thieno[3′,4′:5,6][1,4]dithiino[2,3-b]quinoxaline: a joint experimental a…

2000

The novel annelated monomer thieno[3′,4′:5,6][1,4]dithiino[2,3-b]quinoxaline 1 has been electropolymerised on a variety of electrodes, resulting in films which are electroactive in non-aqueous and aqueous solution. The polymer films exhibit a transformation in voltammetric response corresponding to a positive shift in redox potential in the presence of silver cation, the maximum shift being ca. 150 mV in acetonitrile and ca. 400 mV in aqueous LiClO4 solution. Mercury dication demonstrates a similar, but smaller (ca. 130 mV) shift in aqueous solution. Theoretical calculations clearly show the potential of poly(1) as a metal complexation agent. The Ag+ ion coordinates with 1 in two ways: (i) …

Aqueous solutionChemistryMetal ions in aqueous solutionTrimerGeneral ChemistryElectrochemistryDicationchemistry.chemical_compoundCrystallographyQuinoxalineMonomerMaterials ChemistryOrganic chemistryAcetonitrileJournal of Materials Chemistry
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Molecular simulation studies of water physisorption in zeolites

2006

We report a series of Grand Canonical Monte Carlo simulations of water adsorption in NaY and NaX faujasite, as well as in silicalite-1. Computed adsorption isotherms and heats of adsorption were in good agreement with the available experiments. The existence of cyclic water hexamers in NaX located in the 12-ring windows, recently disclosed by neutron diffraction experiments (Hunger et al., J. Phys. Chem. B, 2006, 110, 342-353) was reproduced in our simulations. Interestingly enough, such cyclic hexamer clusters were also observed in the case of NaY, in which no stabilizing cation is present in the 12-ring window. We also report cation redistribution upon water adsorption for sodium faujasit…

Aqueous solutionChemistryNeutron diffractionGeneral Physics and Astronomy02 engineering and technologyFaujasiteengineering.material010402 general chemistry021001 nanoscience & nanotechnologyMolecular sieve01 natural sciences0104 chemical sciencesSeparation processAdsorptionPhysisorptionengineeringPhysical chemistryPhysical and Theoretical Chemistry0210 nano-technologyZeolitePhysical Chemistry Chemical Physics
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Application of the small-angle neutron scattering technique to the study of solubilization mechanisms of organic molecules by micellar systems

1996

Abstract We present the possible contribution of the small-angle neutron scattering (SANS) technique to the molecular interpretation of the solubilization phenomena in simple micellar systems. We show for a few ternary micellar systems, that an appropriate analysis of SANS experimental data can provide information on modifications induced on micellar dimension, shape, number of monomer, and charge and on the partition coefficient of the additive and its localization inside the micellar aggregate. The influence of n -alcohols on the thermodynamics and on the structure of sodium dodecyl sulphate (SDS) aqueous solution has been extensively investigated, so the agreement between the results obt…

Aqueous solutionChemistryOrganic ChemistryInorganic chemistryAqueous two-phase systemNeutron scatteringMicelleSmall-angle neutron scatteringAnalytical ChemistryInorganic ChemistryPartition coefficientChemical physicsPhase (matter)Ternary operationSpectroscopyJournal of Molecular Structure
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Hole Localization and Thermochemistry of Oxidative Dehydrogenation of Aqueous Rutile TiO2(110)

2012

Aqueous solutionChemistryOrganic ChemistryOxidative phosphorylationPhotochemistryCatalysisInorganic ChemistryComputational chemistryRutileThermochemistryDensity functional theoryDehydrogenationPhysical and Theoretical ChemistryProton-coupled electron transferChemCatChem
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