Search results for "Kinetic"

showing 10 items of 3064 documents

Micellar Liquid Chromatography: Fundamentals

2015

The reversed phase liquid chromatography (RPLC) mode with surfactant above the critical micellar concentration (CMC) has been called micellar liquid chromatography (MLC). In pure micellar systems, the retention behavior is explained by considering three phases or environments: surfactant-modified stationary phase, bulk aqueous solvent, and micellar pseudo-phase. Surfactant adsorption on the porous RPLC packing affects chromatographic retention, owing to the change of diverse surface properties of the stationary phase. In pure micellar systems, the retention behavior is explained by considering three phases or environments: surfactant-modified stationary phase, bulk aqueous solvent, and mice…

Aqueous solutionColumn chromatographyAqueous normal-phase chromatographyChemistryMicellar liquid chromatographyHydrophilic interaction chromatographytechnology industry and agricultureAnalytical chemistrylipids (amino acids peptides and proteins)macromolecular substancesReversed-phase chromatographyMicelleMicellar electrokinetic chromatography
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Influence of Phase Modifiers on the Degradation of Tri-n-octylamine/dodecane Extracting Mixture by an Acidic Solution of Vanadium (V)

2012

The kinetics of degradation of a mixture of tri-n-octylamine (extractant) and various alcoholic phase modifiers in n-dodecane in contact with acidic aqueous sulfate solutions containing vanadium (V) has been investigated. The nature of the modifier influences the kinetics of degradation and an improvement of the resistance against the chemical degradation is obtained when secondary alcohol (2-nonanol) or tertiary alcohols such as 9-octyl-9-heptadecanol are used as phase modifiers instead of 1-tridecanol. For instance, the kinetic constant of degradation is divided by one half when 9-octyl-9-heptadecanol is used as phase modifier instead of 1-tridecanol. On the contrary, the alcohols contain…

Aqueous solutionDodecaneGeneral Chemical EngineeringKineticsInorganic chemistryVanadiumchemistry.chemical_elementAlcoholGeneral ChemistrySolventchemistry.chemical_compoundchemistryPhase (matter)Chemical decompositionSolvent Extraction and Ion Exchange
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Crystallization of the CaCO3 mineral in the presence of the protein ovalbumin

2004

Abstract The kinetics of CaCO3 mineralization was studied by SANS in a 0.1 M aqueous CaCl2 solution in the presence of the protein ovalbumin found in chicken eggs. As the scattering from the protein and the mineral was observed within different Q regimes the evolution of the protein and mineral could be followed independently. It is observed that ovalbumin denaturates during the first 3 h and leads to a strong enhancement of mineralization.

Aqueous solutionMineralbiologyChemistryKineticsMineralization (soil science)Condensed Matter PhysicsElectronic Optical and Magnetic Materialslaw.inventionOvalbuminlawbiology.proteinElectrical and Electronic EngineeringCrystallizationBiomineralizationNuclear chemistryPhysica B: Condensed Matter
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Zeta-Potential Study of Calcium Silicate Hydrates Interacting with Alkaline Cations

2001

An investigation into the interaction between alkaline cations and calcium silicate hydrates (CSH) was conducted by electrokinetic measurements, which provided information on the nature of the interface between the solid and its equilibrium solution. Calcium constitutes for the CSH surface a potential-determining cation. A model of the CSH surface could be proposed, accounting for the experimental evolution of the CSH zeta potential. The necessity of studying the zeta-potential evolution of the system as a function of the calcium activity, instead of its concentration, was underlined. The results obtained suggest a specific interaction between cesium and the CSH surface, whereas sodium and …

Aqueous solutionSodiumInorganic chemistrychemistry.chemical_elementCalciumSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsElectrokinetic phenomenachemistry.chemical_compoundColloid and Surface ChemistrychemistryCalcium silicateZeta potentialLithiumHydrateJournal of Colloid and Interface Science
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Influence of nitrogen and carbon sources on the production of ochratoxin A by ochratoxigenic strains of Aspergillus spp. isolated from grapes.

2008

This work studies the influence of nitrogen and carbon source on ochratoxin A production by three Aspergillus isolates A. ochraceus (Aso2), A. carbonarius (Ac25) and A. tubingensis (Bo66), all isolated from grapes. A basal medium (0.01 g/l FeSO4.7H2O, 0.5 g/l MgSO4.7H2O, 0.5 g/l Na2HPO4.2H2O, 1.0 g/l KCl) was prepared. This medium was supplemented with different nitrogen sources, both inorganic [(NH4)3PO(4), 0.3 g/l plus NH4NO3, 0.2 g/l] and organic (histidine, proline, arginine, phenylalanine, tryptophan or tyrosine) at two concentrations (0.05 g/l or 0.3 g/l), and different carbon sources (sucrose, glucose, maltose, arabinose or fructose) at three concentrations (10 g/l, 50 g/l or 150 g/l…

ArabinoseOchratoxin ASucroseNitrogenColony Count MicrobialPhenylalanineBiologyMicrobiologychemistry.chemical_compoundBotanyVitisFood scienceIncubationOchratoxinAnalysis of VarianceDose-Response Relationship DrugFructoseGeneral MedicineMaltoseOchratoxinsCarbonCulture MediaKineticsAspergilluschemistryFood MicrobiologyFood ScienceChromatography LiquidInternational journal of food microbiology
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Voltage dependence of L-arginine transport by hCAT-2A and hCAT-2B expressed in oocytes from Xenopus laevis.

2000

Membrane potential and currents were investigated with the two-electrode voltage-clamp technique in Xenopus laevisoocytes expressing hCAT-2A or hCAT-2B, the splice variants of the human cationic amino acid transporter hCAT-2. Both hCAT-2A- and hCAT-2B-expressing oocytes exhibited a negative extracellularl-arginine concentration ([l-Arg]o)-sensitive membrane potential, additive to the K+diffusion potential, when cells were incubated in Leibovitz medium (containing 1.45 mM l-Arg and 0.25 mM l-lysine). The two carrier proteins produced inward and outward currents, which were dependent on the l-Arg gradient and membrane potential. Ion substitution experiments showed that the hCAT-induced curren…

ArgininePhysiologyXenopusBiologyArginineL-arginine transportXenopus laevisElectrochemistryAnimalsHumansProtein IsoformsspliceAmino acid transporterMembrane potentialMembrane ProteinsBiological TransportCell BiologyMembrane transportbiology.organism_classificationIn vitroCell biologyElectrophysiologyKineticsBiochemistryOocytesAmino Acid Transport Systems BasicFemaleCarrier ProteinsAmerican journal of physiology. Cell physiology
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INFγ stimulates arginine transport through system y+L in human monocytes

2004

Freshly isolated human monocytes transport L-arginine mostly through a sodium independent, NEM insensitive pathway inhibited by L-leucine in the presence, but not in the absence of sodium. Interferon-gamma (IFNgamma) stimulates this pathway, identifiable with system y+L, and markedly enhances the expression of SLC7A7, the gene that encodes for system y+L subunit y+LAT1, but not of SLC7A6, that codes for the alternative subunit y+LAT2. System y+ plays a minor role in arginine uptake by monocytes and the expression of system y+-related genes, SLC7A1 and SLC7A2, is not changed by IFNgamma. These results demonstrate that system y+L is sensitive to IFNgamma.

ArginineSodiumProtein subunitBiophysicschemistry.chemical_elementBiologyLPI - Lysinuric protein intoleranceArginineMonocyteBiochemistryMonocytesInterferon-gammaInterferon γLeucineStructural BiologyArginine transportSystem y+L.GeneticsmedicineHumansMolecular BiologyGeneLysinuric protein intoleranceCells CulturedArginine transportReverse Transcriptase Polymerase Chain ReactionFusion Regulatory Protein 1 Light ChainsMonocyteSodiumAmino Acid Transport System y+LBiological TransportCell BiologyMolecular biologyRecombinant ProteinsKineticsmedicine.anatomical_structurechemistryEthylmaleimideAmino Acid Transport Systems BasicInterferon-γFEBS Letters
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Temperature at Small Scales: A Lower Limit for a Thermodynamic Description

2011

We analyze the concept of equilibrium temperature in a set of interacting argon atoms, confined in a nanostructure, a zeolite with an intricate distribution of channels through which the atoms may move. The temperature is computed following two procedures: by averaging over the kinetic energy of the particles and over the forces acting on them. It is shown that for external surfaces and for regions which do not fall under the whole pattern of potential energy distribution, smaller than a quarter of a crystal unit cell, both temperatures, kinetic and configurational, show significant differences. The configurational temperature accounts for the different interactions on the particles in the …

ArgonNanostructureMean kinetic temperatureThermodynamic equilibriumchemistry.chemical_elementThermodynamicsKinetic energyPotential energySurfaces Coatings and FilmsCrystalchemistryNano-Materials ChemistryPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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1989

The reaction kinetics for the group transfer polymerization (GTP) of tert-butyl methacrylate (TBMA) using a silyl ketene acetal initiator and a nucleophilic catalyst are investigated. The reaction is shown to be of first order in both monomer and catalyst concentrations. The “livingness” of this system appears to be influenced by the reaction temperature. At temperatures above −20°C, deactivation is observed, with its severity increasing with increasing temperature. This deactivation is attributed to a depletion of catalyst by side reactions. It was demonstrated that reactivation is made possible by the addition of more catalyst. This result is in contrast to the anionic polymerization of T…

Arrhenius equationChemical kineticssymbols.namesakeReaction mechanismReaction rate constantAnionic addition polymerizationPolymerizationChemistryPolymer chemistrysymbolsSolution polymerizationCatalysisDie Makromolekulare Chemie
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Dependence of O2 diffusion dynamics on pressure and temperature in silica nanoparticles

2013

An experimental study of the molecular O2 diffusion process in high purity non-porous silica nanoparticles having 50 m2/g BET specific surface and 20 nm average radius was carried out in the temperature range from 127 to 177 °C at O2 pressure in the range from 0.2 to 66 bar. The study was performed by measuring the volume average interstitial O2 concentration by a Raman and photoluminescence technique using a 1,064 nm excitation laser to detect the singlet to triplet emission at 1,272 nm of the molecular oxygen in silica. A dependence of the diffusion kinetics on the O2 absolute pressure, in addition to temperature dependence, was found. The kinetics can be fit by the solution of Fick’s dif…

Arrhenius equationDiffusion in nanosilicaDiffusion equationMaterials scienceSettore FIS/01 - Fisica SperimentaleAnalytical chemistryBioengineeringGeneral ChemistryActivation energyAtmospheric temperature rangeCondensed Matter PhysicsAtomic and Molecular Physics and Opticslaw.inventionsymbols.namesakePressure measurementDiffusion processlawModeling and SimulationsymbolsEffective diffusion coefficientNanosilica O2 diffusion Diffusion kinetics Raman spectroscopyGeneral Materials ScienceRaman spectroscopyJournal of Nanoparticle Research
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