Search results for "Aqueous-solution"

showing 10 items of 17 documents

Chemical Identification at the Solid–Liquid Interface

2017

Solid-liquid interfaces are decisive for a wide range of natural and technological processes, including fields as diverse as geochemistry and environmental science as well as catalysis and corrosion protection. Dynamic atomic force microscopy nowadays provides unparalleled structural insights into solid-liquid interfaces, including the solvation structure above the surface. In contrast, chemical identification of individual interfacial atoms still remains a considerable challenge. So far, an identification of chemically alike atoms in a surface alloy has only been demonstrated under well-controlled ultrahigh vacuum conditions. In liquids, the recent advent of three-dimensional force mapping…

CALCIUM-CARBONATEMOLECULAR-DYNAMICS SIMULATIONSSURFACEInterface (Java)AlloyNanotechnology02 engineering and technologyengineering.material010402 general chemistry53001 natural sciencesAQUEOUS-SOLUTIONCorrosionElectrochemistryWATERGeneral Materials ScienceFIELDSpectroscopySpectroscopySolid liquidATOMIC-FORCE MICROSCOPYta114ChemistryAtomic force microscopyHYDRATIONSolvationSurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesRESOLUTIONengineeringIdentification (biology)0210 nano-technologyLangmuir
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Water and temperature contribution to the structuration of starch matrices in the presence of flavour.

2016

The effect of hydrothermal treatments and flavours addition on starch structure and its physical properties were studied. Native wheat starch was treated at 2 different hydrations (water-starch ratios: 50/50 and 80/20 g w/w) and temperatures (65 and 85 °C) in the presence of flavours (ethyl hexanoate and 2-hexanone). The freshly prepared samples were subjected to DSC and flavour analysis. Flavour inclusion complex could not be detected by DSC, however the result of flavour analysis proved that there were flavours interactions with starch. Both ethyl hexanoate and 2-hexanone interacted with starch at similar rates. The highest flavour loss was found in the samples at high hydration and heate…

GelatinizationStarchPhysicochemical propertiesFlavourAmylopectinAqueous-solutionsAnalytical Chemistrychemistry.chemical_compoundCrystallinity0404 agricultural biotechnologyPartial gelatinisationComplexesAmylose[SDV.IDA]Life Sciences [q-bio]/Food engineeringFreezingChromatographyThermomechanical behaviorChemistrySmall-angle X-ray scatteringGranule (cell biology)Wheat starch[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringTemperatureEthyl hexanoateWaterStarch04 agricultural and veterinary sciencesGeneral MedicineHeat-moisture treatment040401 food sciencePasting propertiesRVAAroma compoundsAmylopectinTasteFlavourAmyloseFood ScienceNuclear chemistryFood chemistry
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Low-cost materials for boron adsorption from water

2012

[EN] Knowing the affinity of boron aqueous species for cis-diol organic groups, five different hybrid materials have been prepared by anchoring glucose groups onto the surface of silica matrices with a different surface topology: UVM-7 bimodal mesoporous silica, UVM-11 unimodal non-templated mesoporous silica, commercial silica fume and two silica xerogels with pores within the mesoporous range (13-50 nm). After optimizing the experimental conditions, a comparison was made of the boron adsorption capacities in water. The relationship of the structural and functionalization parameters is discussed and the importance of the surface topology in the final adsorption behaviour is revealed. Hence…

INGENIERIA DE LA CONSTRUCCIONMaterials scienceSilica fumeInorganic chemistrychemistry.chemical_elementAdsorptionQUIMICA ORGANICAMaterials ChemistryReverse-OsmosisNanoparticulated SilicasBoronChemical ControlAzomethine-H MethodAqueous-SolutionQUIMICA INORGANICAGeneral ChemistryMesoporous silicaMesoporous organosilicachemistryMesoporous OxidesSurface-PropertiesSurface modificationMesoporous materialHybrid materialRemovalPorosityIon-Exchange
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Structural Organization of Poly(vinyl alcohol) Hydrogels Obtained by Freezing and Thawing Techniques:  A SANS Study

2005

The structural organization of matter in poly(vinyl alcohol) (PVA) hydrogels obtained by repeatedly freezing and thawing dilute solutions of PVA in D2O is investigated by use of small-angle neutron scattering measurements (SANS). This study is the first systematic and quantitative investigation in the medium range of length scales on PVA hydrogels obtained by freezing and thawing techniques. The studied gels have a complex hierarchical structure, extending over a wide range of length scales. The structural organization on the micron length scale originates from the presence of two separated phases constituted by polymer-rich and polymer-poor regions. The network structure may be interpreted…

Length scaleVinyl alcoholMaterials sciencenanostructureGeneral Chemical EngineeringNeutron scatteringPOLYVINYL-ALCOHOL) GELSGELATION PROCESSchemistry.chemical_compoundPhase (matter)AQUEOUS-SOLUTIONSPolymer chemistryMaterials ChemistrySMALL-ANGLE NEUTRONStructural organizationGeneral ChemistryLIGHT-SCATTERINGCondensed Matter::Soft Condensed MatterChemical engineeringchemistryMedium rangeSelf-healing hydrogelsSmall-angle neutron scatteringMORPHOLOGYCrystallitehydrogelPHASE-SEPARATIONChemistry of Materials
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A multifuctional nanoplatform for drug targeted delivery based on radiation-engineered nanogels

2020

Abstract Under a rational design, combining biologically active molecules, ligands to specific cell receptors and fluorescent, radioactive or paramagnetic labels into a single nano-object can bridge the unique properties of the individual components and improve conventional sensing, imaging and therapeutic efficacies. The validation of these functional nano-objects requires careful testing both in terms of physico-chemical properties and biological behaviour in vitro and in vivo, prior to translation into the clinic. Ionising radiation of aqueous polymer solutions is a viable strategy to produce multifunctional nanogels from aqueous solutions of hydrophilic polymers. By proper selection of …

COLON-CANCER CELLSPULSE-RADIOLYSISDrugINDUCED CROSS-LINKINGSPECTRAL PROPERTIESmedia_common.quotation_subjectNanogelsConjugation reactionsNanotechnology01 natural sciencesAQUEOUS-SOLUTIONFLUORESCEIN030218 nuclear medicine & medical imagingNanogel03 medical and health sciences0302 clinical medicineHydrophilic polymers0103 physical sciencesNANOPARTICLESMoleculeIonising radiation synthesiIN-VIVOmedia_commonchemistry.chemical_classificationRadiationAqueous solution010308 nuclear & particles physicsIonising radiation synthesisRational designPolymerINSULINNanomedicineConjugation reactionchemistryDrug deliveryDrug deliveryNanomedicineSettore CHIM/07 - Fondamenti Chimici Delle TecnologieACID) NANOGELSRadiation Physics and Chemistry
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Ultrasound-assisted MnO2 catalyzed homolysis of peracetic acid for phenol degradation: The assessment of process chemistry and kinetics

2013

Abstract The combination of peracetic acid (PAA) and heterogeneous catalyst (MnO 2 ) was used for the degradation of phenol in an aqueous solution in the presence of ultrasound irradiation (US). As a relevant source of free radicals (e.g. OH), peracetic acid was comprehensively studied by means of electron spin resonance (ESR) spin trapping (ST) techniques with the subsequent identification of free radicals by simulation based fitting (SBF) technique. The radical reaction mechanism, where hydroxyl radical was a primary product of O O bond rupture of PAA, was established taking into account radical reactions, occurring during sonolysis. The potential barriers and the reaction heat were deter…

General Chemical EngineeringRadicalwaterBiophysicsmechanismPhotochemistryIndustrial and Manufacturing EngineeringCatalysisSonochemistrychemistry.chemical_compoundPeracetic acidfree-radicalsintermediateEnvironmental ChemistryPhenolLaboratorium voor Plantenfysiologieta116decompositionSpin trappingChemistryaqueous-solutionsGeneral ChemistrydestructionHomolysisBiofysicasystemsHydroxyl radicalwet peroxide oxidationsonochemistryLaboratory of Plant PhysiologyChemical Engineering Journal
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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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Polystyrene nanoparticles in the presence of (ethylene oxide)13(propylene oxide)30(ethylene oxide)13, N,N-dimethyloctylamine-N-oxide and their mixtur…

2008

Polystyrene nanoparticles were synthesized by emulsion polymerization of styrene. They were functionalized using the conventional surfactant N,N-dimethyloctylamine-N-oxide (ODAO), the tri-block copolymer (ethylene oxide)13(propylene oxide)30(ethylene oxide)13 (L64) and their mixtures. To this purpose, dynamic light scattering and calorimetric experiments were carried out and provided information consistent to each other. The L64 adsorption is Langmuir-type in the copolymer dilute regime and generates complex structures at larger concentrations. In the region where ODAO is in the unimeric state, the adsorption process is cooperative leading to hemi-micelle formation at the polystyrene nanopa…

Ethylene OxideMaterials scienceLightSurface PropertiesOxideGeneral Physics and AstronomyEmulsion polymerizationCalorimetryTRIBLOCK COPOLYMERSStyrenechemistry.chemical_compoundDynamic light scatteringAQUEOUS-SOLUTIONSPolymer chemistryCopolymerScattering RadiationPropylene oxideSURFACTANTSPhysical and Theoretical ChemistryStyreneEthylene oxideLAPONITE CLAYWaterOxidesOctanesHEAT-CAPACITIESSolutionsBLOCK-COPOLYMERSLATEXchemistryChemical engineeringNanoparticlesPolystyrenesMASS-ACTION MODELTHERMODYNAMIC PROPERTIESAdsorptionPolystyrenePhys. Chem. Chem. Phys.
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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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