Search results for "Aqueous-solution"

showing 7 items of 17 documents

Highly stable and porous porphyrin-based zirconium and hafnium phosphonates – electron crystallography as an important tool for structure elucidation

2018

The Ni-metallated porphyrin-based tetraphosphonic acid (Ni-tetra(4-phosphonophenyl)porphyrin, Ni-H8TPPP) was used for the synthesis of highly porous metal phosphonates containing the tetravalent cations Zr4+ and Hf4+. The compounds were thoroughly characterized regarding their sorption properties towards N2 and H2O as well as thermal and chemical stability. During the synthesis optimization the reaction time could be substantially decreased under stirring from 24 to 3 h in glass vials. M-CAU-30, [M2(Ni-H2TPPP)(OH/F)2]·H2O (M = Zr, Hf) shows exceptionally high specific surface areas for metal phosphonates of aBET = 1070 and 1030 m2 g-1 for Zr- and Hf-CAU-30, respectively, which are very clos…

PORESMaterials scienceChemistry Multidisciplinarychemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesAQUEOUS-SOLUTIONMETAL-ORGANIC FRAMEWORKSchemistry.chemical_compoundDESIGNAUTOMATED DIFFRACTION TOMOGRAPHYFormula unitMoleculeCRYSTAL-STRUCTUREZirconiumScience & TechnologySTABILITYGeneral Chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencesChemistryMANGANESE PORPHYRINSCrystallographychemistryElectron diffractionPhysical SciencesLIGANDSChemical stabilityCyclic voltammetry0210 nano-technologySYSTEMChemical Science
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Thermodynamics of Proton Binding of Halloysite Nanotubes

2016

In this paper, new information on physical and chemical properties of the widely used nanostructured Halloysite mineral are reported. Given that the Halloysite has a tubular structure formed by a variable number of wrapped layers containing Si-OH and Al-OH groups, their proton binding affinity was measured at different ionic strengths and ionic media by means of potentiometric measurements in heterogeneous phase. One protonation constant for the Si-OH groups and two for the Al-OH groups were determined. The protonation constant values increase with increasing of the ionic strength in all the ionic media. This suggests that the presence of a background electrolyte stabilizes the protonated s…

Proton bindingInorganic chemistrySurfaces Coatings and FilmIonic bondingProtonation02 engineering and technologyElectrolyteengineering.material010402 general chemistry01 natural sciencesHalloysiteIonSettore CHIM/01 - Chimica AnaliticaSurface chargePhysical and Theoretical ChemistrySettore CHIM/02 - Chimica FisicaChemistryElectronic Optical and Magnetic Material021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnergy (all)General EnergyIonic strengthengineering0210 nano-technologyACID-BASE PROPERTIES; MOLECULAR-WEIGHT LIGANDS; CLAY NANOTUBES; AQUEOUS-SOLUTION; IONIC-STRENGTH; ACTIVITY-COEFFICIENTS; WEAK COMPLEXES; FORMATION-CONSTANTS; CONTROLLED-RELEASE; SUSTAINED-RELEASE
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Thermal potential of ion-exchange membranes and its application to thermoelectric power generation

2016

The low efficiency and high price of thermoelectric semiconductors has generated interest in unconventional forms of thermoelectric materials. In this article, ionic thermoelectricity has been studied with commercial ion-exchange membranes for different aqueous 1:1 electrolytes. The theory of thermal membrane potential has been derived taking into account the ionic heats of transport, the non-isothermal Donnan potentials, the temperature polarization, and the thermally-induced concentration polarization of the electrolyte. Also the generated thermoelectric power has been experimentally studied. The experiments show good agreement with the theory, and suggest ways for systematic improvement …

TRANSPORTED ENTROPYNon-isothermal electrodiffusionHALIDE SOLUTIONSThermodynamicsFiltration and Separation02 engineering and technologyElectrolyte010402 general chemistry01 natural sciencesBiochemistrySeebeck coefficientThermoelectric effectAQUEOUS-SOLUTIONSGeneral Materials SciencePhysical and Theoretical ChemistryPolarization (electrochemistry)NONISOTHERMAL SYSTEMSta116Concentration polarizationIonic heat of transportChemistryTEMPERATURE POLARIZATIONThermal membrane potentialThermoelectric power generation021001 nanoscience & nanotechnologyThermoelectric materialsELECTROLYTE-SOLUTIONSSODIUM-CHLORIDE0104 chemical sciencesIonic Seebeck coefficientThermoelectric generatorMembraneMASS-TRANSPORTIon-exchange membranes0210 nano-technologyCHARGED MEMBRANESSORET COEFFICIENTSJOURNAL OF MEMBRANE SCIENCE
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A metal-responsive interdigitated bilayer for selective quantification of mercury( ii ) traces by surface plasmon resonance

2016

Reusable surface plasmon resonance chips allowing the quantitative and selective detection of mercury(II) ions in water at the 0.01 nM level are reported. The surface-modified gold sensor consists of a rarefied self-assembled monolayer of octanethiol topped with a Langmuir–Blodgett monolayer of an amphiphilic and highly-specific chelator. The interdigitated architecture confers to the bilayer a high packing density, surface coverage, and binding-group accessibility.

aqueous-solutionwaterAnalytical chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesBiochemistryAnalytical ChemistryIonsensoroptical-detectionMonolayerAmphiphilevoltammetric determinationElectrochemistryEnvironmental Chemistry[CHIM]Chemical SciencesChelationSurface plasmon resonanceSpectroscopyimpedance spectroscopyBilayerself-assembled monolayerssprgold021001 nanoscience & nanotechnology0104 chemical sciencesMercury (element)chemistryions0210 nano-technology
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Adsorption of triblock copolymers and their homopolymers at laponite clay/solution interface. Role played by the copolymer nature

2009

The adsorption thermodynamics of copolymers, based on ethylene oxide (EO) and propylene oxide ( PO) units, at the laponite (RD) clay/liquid interface was determined at 298 K. The copolymer nature was tuned at molecular level by changing the hydrophilicity, the architecture and the molecular weight (Mw) keeping constant the EO/PO ratio. Polyethylene (PEGs) and polypropylene (PPGs) glycols with varying Mw and their mixture were also investigated to discriminate the role of the EO and the PO segments in the adsorption process. Enthalpies of transfer of RD, at fixed concentration, from water to the aqueous macromolecule solutions as functions of the macromolecule molality were determined. They …

chemistry.chemical_classificationAqueous solutionEthylene oxideGeneral Physics and AstronomyPolymerSURFACTANT INTERACTIONSANGLE NEUTRON-SCATTERINGCLAY PARTICLESHEAT-CAPACITIESBLOCK-COPOLYMERSchemistry.chemical_compoundAdsorptionchemistryChemical engineeringCONCENTRATION RANGEAQUEOUS-SOLUTIONSPolymer chemistryCopolymerPOLY(ETHYLENE OXIDE)Propylene oxideOXIDE)(13)-(PROPYLENE OXIDE)(30)-(ETHYLENE OXIDE)(13)SODIUM DODECYL-SULFATEPhysical and Theoretical ChemistryEquilibrium constantMacromoleculePhysical Chemistry Chemical Physics
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Structural behaviour differences in low methoxy pectin solutions in the presence of divalent cations (Ca 2+ and Zn 2+ ): a process driven by the bind…

2014

International audience; In this paper, we compare the interactions between low methoxy pectin (LMP) and either Ca2+ or Zn2+ in semi-dilute solutions. Intrinsic viscosity and turbidity measurements reveal that pectin-calcium solutions are more viscous, but yet less turbid, than pectin-zinc ones. To get a molecular understanding on the origin of this rather unexpected behavior, we further performed isothermal titration calorimetry, small angle neutron scattering experiments, as well as molecular dynamics simulations. Our results suggest that calcium cations induce the formation of a more homogeneous network of pectin than zinc cations do. The molecular dynamics simulations indicate that this …

food.ingredientGelationPectinInorganic chemistryEgg-box modelchemistry.chemical_elementZincMolecular Dynamics SimulationCalciumAqueous-solutionsInsightsDivalentAssociationScatteringMolecular dynamicschemistry.chemical_compoundfoodPolysaccharides[SDV.IDA]Life Sciences [q-bio]/Food engineeringMoleculeCarboxylateAlginate gelschemistry.chemical_classificationViscosityHexuronic AcidsIsothermal titration calorimetryGeneral ChemistryCondensed Matter PhysicsDrug-deliverySolutionsZincCrystallographychemistryPectinsCalcium
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Micelles in Mixtures of Sodium Dodecyl Sulfate and a Bolaform Surfactant

2006

Mixtures composed of water, sodium dodecyl sulfate (SDS), and a bolaform surfactant with two aza-crown ethers as polar headgroups (termed Bola C-16) were investigated by modulating the mole ratios between the components. The two surfactants have ionic and nonionic, but ionizable, headgroups, respectively. The ionization is due to the complexation of alkali ions by the aza-crown ether unit(s). Structural, thermodynamic, and transport properties of the above mixtures were investigated. Results from surface tension, translational self-diffusion, and small angle neutron scattering ( SANS) are reported and discussed. Interactions between the two surfactants to form mixed micelles result in a com…

mixed micellesIonic bondingEtherANGLE NEUTRON-SCATTERINGMicelleanionic surfactants; mixed micelles; neutron scatteringSurface tensionSurface-Active Agentschemistry.chemical_compoundPulmonary surfactantAQUEOUS-SOLUTIONSSodium sulfateanionic surfactantsElectrochemistrySurface TensionGeneral Materials ScienceSodium dodecyl sulfateSANS surfactant mixtures micellesMicellesSpectroscopyHYDROCARBON SURFACTANTSPHASE SEPARATION MODELChromatographyneutron scatteringSodium Dodecyl SulfateSurfaces and InterfacesCondensed Matter PhysicsSmall-angle neutron scatteringchemistryChemical engineeringLangmuir
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