Search results for "Surfaces"

showing 10 items of 2837 documents

Spatio-temporal perturbation of the dynamics of the ferroin catalyzed Belousov-Zhabotinsky reaction in a batch reactor caused by sodium dodecyl sulfa…

2008

The effects of the anionic surfactant sodium dodecyl sulfate (SDS) on the spatio-temporal and temporal dynamics of the ferroin-catalyzed Belousov-Zhabotinsky (BZ) reaction have been studied over a wide surfactant concentration range. For the first time, investigations were performed also for unstirred systems. The presence of SDS in the reaction mixture influences the oscillatory parameters to an extent that significantly depends on the surfactant concentration. The trend of the wave speed v upon the increasing amount of SDS was found to have a maximum at [SDS] = 0.075 mol dm (-3) ( v = 0.071 mm s (-1)), after which the speed decreased to 0.043 mm s (-1) at [SDS] = 0.5 mol dm (-3), which is…

Inorganic chemistryBatch reactorsodium dodecyl sulfate Belousov-Zhabotinsky non-linear dynamicsMicelleSurfaces Coatings and FilmsCatalysischemistry.chemical_compoundBelousov–Zhabotinsky reactionchemistryPulmonary surfactantFerroinMaterials ChemistryPhysical and Theoretical ChemistrySodium dodecyl sulfateThe journal of physical chemistry. B
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Experimental and theoretical study using DFT method for the competitive adsorption of two cationic dyes from wastewaters

2016

Abstract The adsorption of cationic dyes, Basic Yellow (BY28) and Methylene Blue (MB) on a new activated carbon from medlar species were studied in both single and binary system. Some experimental parameters, namely, pH, amount of adsorbent and contact time are studied. Quantum chemical results indicate that the adsorption efficiency was directly related to the dye electrophilicity power. Some theorical parameters were calculated and proved that MB is more electrophilic than BY28, than greatest interaction with surface sites. Kinetic study showed that the adsorption follows the pseudo-second-order model and Freundlich was the best model to describe the phenomenon in the single and binary sy…

Inorganic chemistryCationic polymerizationGeneral Physics and Astronomy02 engineering and technologySurfaces and InterfacesGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSurfaces Coatings and Filmschemistry.chemical_compoundAdsorptionchemistryElectrophilemedicineFreundlich equationReactivity (chemistry)Binary system0210 nano-technologyMethylene blueActivated carbonmedicine.drugApplied Surface Science
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Controlling the cohesion of cement paste

2005

The main source of cohesion in cement paste is the nanoparticles of calcium silicate hydrate (C-S-H), which are formed upon the dissolution of the original tricalcium silicate (C(3)S). The interaction between highly charged C-S-H particles in the presence of divalent calcium counterions is strongly attractive because of ion-ion correlations and a negligible entropic repulsion. Traditional double-layer theory based on the Poisson-Boltzmann equation becomes qualitatively incorrect in these systems. Monte Carlo (MC) simulations in the framework of the primitive model of electrolyte solution is then an alternative, where ion-ion correlations are properly included. In addition to divalent calciu…

Inorganic chemistryIonic bonding02 engineering and technologyElectrolyteCement pasteCSH010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundlawElectrochemistryGeneral Materials Sciencecalcium silicate hydrateCalcium silicate hydrateDissolutionionic correlationsSpectroscopyion-ion correlations[CHIM.MATE] Chemical Sciences/Material chemistrySurfaces and Interfaces[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPotassium sulfateSilicate0104 chemical sciencesC-S-HPortland cementchemistryChemical engineering[ CHIM.MATE ] Chemical Sciences/Material chemistryCalcium silicatenanoparticles0210 nano-technologycement cohesioncharge reversal
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Ionic and Free Solvent Motion in Poly(azure A) Studied by ac-Electrogravimetry

2011

International audience; This work is focused on the mechanistic aspects of the redox behavior of poly(azure A) taking advantage of the controlled modulation of their oxidation states by ac-electrogravimetry. The originality of this technique is its ability to discriminate between cation and anion involved in the charge compensation process and the accompanying free solvent transfer, directly or indirectly. Two processes were proposed where the faster ionic exchange is considered to be the participation of the anion species acting as counterions whereas the slower one is related to the proton transfer. The proton is implied as reactants for the two electroactive sites identified in the polym…

Inorganic chemistryIonic bondingAzure A02 engineering and technology010402 general chemistry01 natural sciencesRedoxIonchemistry.chemical_compoundQUARTZ-CRYSTAL MICROBALANCEElectrogravimetryPOLYMER-MODIFIED ELECTRODESPhysical and Theoretical ChemistryELECTROACTIVE THIN-FILMSchemistry.chemical_classificationAqueous solutionPRUSSIAN BLUE021001 nanoscience & nanotechnologyPOLY(NEUTRAL RED)0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventGeneral EnergyELECTROCHEMICAL POLYMERIZATIONTECHNIQUES ELECTRICAL CHARGEchemistryCONDUCTING POLYMERSCounterion[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyELECTROPOLYMERIZED AZINESINNOVATIVE COMBINATIONThe Journal of Physical Chemistry C
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Easy Route to Functionalize Iron Oxide Nanoparticles via Long-Term Stable Thiol Groups

2009

International audience; The functionalization of superparamagnetic iron oxide nanoparticles (SPIOs) by meso-2,3-dimercaptosuccinic acid (DMSA) was investigated. Under ambient conditions, the thiol groups from DMSA are not stable and do not allow a direct functionalization without storage in stringent conditions or a chemical regeneration of free thiols. In this study, we have developed a protocol based on poly(ethylene glycol) (PEG) grafting of SPIO prior to DMSA anchoring. We have observed that PEG helps to increase the stability of thiol groups under ambient conditions. The thiol functionalized SPIOs were stable under physiological pH and ionic strength as determined by Ellman's essay and…

Inorganic chemistryIron oxide02 engineering and technology010402 general chemistryFerric Compounds01 natural scienceschemistry.chemical_compoundPEG ratioElectrochemistryReactive dyeGeneral Materials ScienceSulfhydryl CompoundsSpectroscopychemistry.chemical_classificationMolecular Structure[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry[CHIM.MATE]Chemical Sciences/Material chemistrySurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter PhysicsCombinatorial chemistry0104 chemical sciencesModels ChemicalchemistryIonic strength[ CHIM.MATE ] Chemical Sciences/Material chemistryThiolNanoparticlesSurface modificationSuccimer0210 nano-technologyEthylene glycolIron oxide nanoparticlesLangmuir
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Versatile wet-chemical synthesis of non-agglomerated CaCO3 vaterite nanoparticles.

2011

Calcium carbonate (vaterite) nanoparticles of 20-60 nm size were obtained without stabilizing tensides by heating a dispersion of calcium bicarbonate (CaHCO(3)) in ethylene glycol for 30 minutes at 40 to 100 °C.

Inorganic chemistryMetals and AlloysNanoparticleGeneral ChemistryChemical synthesisCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCalcium carbonatechemistryCalcium bicarbonateVateriteMaterials ChemistryCeramics and CompositesDispersion (chemistry)Ethylene glycolChemical communications (Cambridge, England)
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A new Co(ii) coordination solid with mixed oxygen, carboxylate, pyridine and thiolate donors exhibiting canted antiferromagnetism with TC≈ 68 K

2006

Reaction of Co(II) chloride with the sodium salt of 2-mercaptonicotinic acid in water at 200 degrees C results in the formation of Co4(2-mna)4(H2O), which orders as a canted antiferromagnet at 68 K.

Inorganic chemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryChlorideOxygenCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSodium saltchemistry.chemical_compoundchemistryPyridinePolymer chemistryMaterials ChemistryCeramics and CompositesmedicineAntiferromagnetismCarboxylatemedicine.drugChemical Communications
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Interaction of Alkaline Metal Cations with Oxidic Surfaces: Effect on the Morphology of SnO2 Nanoparticles

2010

Reaction pathways to SnO(2) nanomaterials through the hydrolysis of hydrated tin tetrachloride precursors were investigated. The products were prepared solvothermally starting from hydrated tin tetrachloride and various (e.g., alkali) hydroxides. The influence of the precursor base on the final morphology of the nanomaterials was studied. X-ray powder diffraction (XRD) data indicated the formation of rutile-type SnO(2). Transmission electron microscopy (TEM) studies revealed different morphologies that were formed with different precursor base cations. Data from molecular dynamics (MD) simulations provide theoretical evidence that the adsorption of the cations of the precursor base to the f…

Inorganic chemistryNanoparticlechemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsTin oxideNanomaterialsAdsorptionchemistryTransmission electron microscopyTetrachlorideElectrochemistryGeneral Materials ScienceTinSpectroscopyPowder diffraction
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Role of Deprotonation and Cu Adatom Migration in Determining the Reaction Pathways of Oxalic Acid Adsorption on Cu(111)

2011

Scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), and first principles theoretical calculations have been used to gain insight into the fundamental processes involved in the adsorption and self-assembly of oxalic acid on Cu(111). The experimental data demonstrate that several reaction pathways are involved in the chemisorption of oxalic acid on Cu(111), one of which leads to deprotonation of the acid into oxalate molecules that form ordered structures on the surface. Theoretical calculations indicate that the adsorption of oxalate molecules is not stable on the surface unless copper adatoms are taken into consideration. Coordination with copper adatoms prevents ox…

Inorganic chemistryOxalic acidPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundGeneral EnergyAdsorptionDeprotonationchemistryX-ray photoelectron spectroscopylawPhysical and Theoretical ChemistryScanning tunneling microscopeThe Journal of Physical Chemistry C
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Influence of Adsorbed Water on the Activation Energy of Model Photocatalytic Reactions

2017

Two commercial (Merck and Sigma-Aldrich) and two home prepared (HP05 and HP05C) powdered TiO2 photocatalysts were investigated by fast field cycling nuclear magnetic resonance experiments in order to explore the nature of the interactions between water and the solid surfaces. The results were related to the activation energies determined at temperatures ranging from 303 to 353 K for the photocatalytic oxidation in water of three model molecules presenting different interactions with the solid surface (catechol, phenol, and metylbenzoate). The photoactivity results at different temperatures were comparable to each other because the runs were carried out while keeping constant the concentrati…

Inorganic chemistrySettore AGR/13 - Chimica Agraria02 engineering and technologyActivation energy010402 general chemistry01 natural sciencesRedoxchemistry.chemical_compoundAdsorptionPhenolMoleculePhysical and Theoretical ChemistryCatecholChemistrygreen chemistrytitanium dioxideSubstrate (chemistry)021001 nanoscience & nanotechnologyNMR0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyPhotocatalysisRelaxomatrySettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologycatalyst
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