Search results for "Kinetic"

showing 10 items of 3064 documents

New insight into δ-Pu alloy oxidation kinetics highlighted by using in-situ X-ray diffraction coupled with an original Rietveld refinement method

2018

Abstract The reactivity of a δ-Pu alloy was studied under dry oxygen at different temperatures. Phase analysis has shown the presence of α-and β-Pu2O3, PuO2, as well as the destabilisation of the δ-phase. The oxidation kinetics were studied using in-situ X-ray diffraction coupled with an original method of Rietveld refinement enabling an individual monitoring of the growth of each oxide. The results have evidenced a parabolic stage resulting from the thickening of the α-Pu2O3 layer, in which a compressive stress state develops. This stage is followed by the linear growth of a porous PuO2 scale.

DiffractionMaterials scienceRietveld refinementGeneral Chemical EngineeringAlloyKineticsAnalytical chemistryOxide02 engineering and technologyGeneral Chemistryengineering.material010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryX-ray crystallographyengineeringGeneral Materials ScienceDestabilisation0210 nano-technologyPorosityCorrosion Science
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Spatiotemporal reaction kinetics of an ultrafast photoreaction pathway visualized by time-resolved liquid x-ray diffraction.

2006

We have studied the reaction dynamics for HgI 2 in methanol by using time-resolved x-ray diffraction (TRXD). Although numerous time-resolved spectroscopic studies have provided ample information about the early dynamics of HgI 2 , a comprehensive reaction mechanism in the solution phase spanning from picoseconds up to microseconds has been lacking. Here we show that TRXD can provide this information directly and quantitatively. Picosecond optical pulses triggered the dissociation of HgI 2 , and 100-ps-long x-ray pulses from a synchrotron probed the evolving structures over a wide temporal range. To theoretically explain the diffracted intensities, the structural signal from the solute, the…

DiffractionMultidisciplinaryChemistrySynchrotronDissociation (chemistry)law.inventionChemical kineticsMicrosecondCrystallographyReaction dynamicslawChemical physicsPicosecondPhysical SciencesUltrashort pulseProceedings of the National Academy of Sciences of the United States of America
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Diffusion of small molecules in edible films: Effect of water and interactions between diffusant and biopolymer

2008

Mass transfers of various molecules in multiphasic food products lead to quality modification and thus require the use of edible films or coatings in-between the foodstuff. Consequently, it is important to assess the barrier properties and efficiencies of edible films as well as to determine the diffusivities of the migrants. Translational diffusion of a reference molecule such as fluorescein, determined by the fluorescence recovery after photobleaching (FRAP) method, displays a threshold of a critical water content inducing an increase of the molecular mobility, and demonstrates that multiple populations of a single molecular specie can be involved in different diffusion kinetics. Further …

DiffusionAnalytical chemistry02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesAnalytical ChemistryMoleculeComputingMilieux_MISCELLANEOUSchemistry.chemical_classification[CHIM.MATE] Chemical Sciences/Material chemistryFluorescence recovery after photobleachingGeneral MedicinePolymer[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologySmall molecule0104 chemical sciencesSolid-state nuclear magnetic resonancechemistryChemical physicsengineeringBiopolymerDiffusion kinetics0210 nano-technologyFood Science
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Kinetics of dimer F2 type center annealing in MgF2 crystals

2018

Authors are greatly indebted to V. Lisitsyn, A. Ch. Lushchik and R.Vila for stimulating discussions. This work has been carried out within the framework of the EUROfusion Consortium and has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement number 633053. The views and opinions expressed herein do not necessarily reflect those of the European Commission. The calculations were performed using facilities of the Stuttgart Supercomputer Center (project DEFTD 12939).

DiffusionAnnealing kinetics:NATURAL SCIENCES:Physics [Research Subject Categories]MgF2F2 centersRadiation defectsF centers
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Efficiency range of the Belousov-Zhabotinsky reaction to induce the self-organization of transient bonds in metallo-supramolecular polymeric systems.

2020

The periodic change of the oxidation state of the metal catalyst in the oscillating Belousov-Zhabotinsky (BZ) reaction has been reported to establish a periodic organization of metallo-supramolecular bonds in polymeric systems, which results in autonomous viscosity oscillations. To appraise the possible extent of quantitative control on the viscosity oscillation features, we assess how the kinetics of the BZ reaction affects the periodic self-organization of the metal-ligand coordination, and vice versa. Our model system includes mono-, bis-, and tetra-functional polyethyleneglycol (PEG) precursors end grafted with terpyridine ligands that are complexed with ruthenium ions, which oscillate …

DiffusionKineticsGeneral Physics and Astronomy02 engineering and technologyReaction intermediate010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesReaction rateViscositychemistry.chemical_compoundBelousov–Zhabotinsky reactionchemistryChemical physicsOxidation statePhysical and Theoretical ChemistryTerpyridine0210 nano-technologyPhysical chemistry chemical physics : PCCP
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Different Sorption Behaviors for Wine Polyphenols in Contact with Oak Wood

2007

The evolution of polyphenols of enological interest- monomeric anthocyanins, (+)-catechin, (-)-epicatechin, gallic acid, and trans-resveratrol-in the presence of oak wood was investigated in aging-model conditions. Disappearance kinetics showed that, except for gallic acid, all of the wine polyphenols tend to disappear from the model wine in presence of oak wood, to reach an equilibrium after 20 days of contact. At equilibrium, the higher disappearance rates were obtained for monomeric anthocyanins and trans-resveratrol with values of 20 and 50%, respectively. For monomeric anthocyanins, the rate of disappearance seemed to be independent of their nature. In order to evaluate the contributio…

DiffusionKineticsSorption kineticsWinecomplex mixturesAnthocyaninschemistry.chemical_compoundQuercusGlucosidesPhenolsBotanyStilbenesGallic acidWineFlavonoidsChemistryExtraction (chemistry)food and beveragesPolyphenolsSorptionGeneral ChemistryWoodKineticsPolyphenolResveratrolEnvironmental chemistryAdsorptionGeneral Agricultural and Biological Sciences
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Synthesis and comparison of the antiinflammatory activity of manoalide and cacospongionolide B analogues.

1998

We have synthesized analogues of two naturally occurring antiinflammatory marine compounds, manoalide and cacospongionolide B, containing a pyranofuranone moiety which is considered the pharmacophoric group. The two compounds, and hence their analogues, differ in the presence or absence in the dihydropyran ring of an hemiacetal function which was considered essential to irreversibly inactivate phospholipase A 2 (PLA 2 ). The two series of compounds were tested for their inhibitory effects on secretory PLA 2 belonging to the groups I, II, and III, and the activities were found to be similar in both series, irrespective of the presence or absence of the additional hemiacetal function. In addi…

DihydropyranStereochemistrySwineCarrageenanChemical synthesisPhospholipases ACell Linechemistry.chemical_compoundManoalideMiceStructure-Activity RelationshipCytosol4-ButyrolactoneDrug DiscoveryMoietyAnimalsEdemaHumansEnzyme InhibitorsPancreasPyranschemistry.chemical_classificationElapid VenomsPhospholipase AbiologyMolecular StructureTerpenesAnti-Inflammatory Agents Non-SteroidalSynovial MembraneBee VenomsKineticsPhospholipases A2chemistryEnzyme inhibitorDrug Designbiology.proteinMolecular MedicineHemiacetalFemaleLactoneJournal of medicinal chemistry
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Unfolding a transmembrane helix dimer: A FRET study in mixed micelles

2009

The exact nature of membrane protein folding and assembly is not understood in detail yet. Addition of SDS to a membrane protein dissolved in mild, non-polar detergent results in formation of mixed micelles and in subsequent denaturation of higher ordered membrane protein structures. The exact nature of this denaturation event is, however, enigmatic, and separation of an individual helix pair in mixed micelles has also not been reported yet. Here we followed unfolding of the human glycophorin A transmembrane helix dimer in mixed micelles by fluorescence spectroscopy. Energy transfer between differently labelled glycophorin A transmembrane helices decreased with increasing SDS mole fractions…

DimerBiophysicsBiochemistryMicelleProtein Structure SecondarySurface-Active Agentschemistry.chemical_compoundFluorescence Resonance Energy TransferHumansGlycophorinGlycophorinsMolecular BiologyMicellesbiologyChemistryPeripheral membrane proteinSodium Dodecyl SulfateTransmembrane proteinProtein Structure TertiaryKineticsTransmembrane domainCrystallographyFörster resonance energy transferMembrane proteinbiology.proteinProtein MultimerizationArchives of Biochemistry and Biophysics
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Die kinetik der allendimerisation, ein beitrag zum mechanismus

1971

Zusammenfassung The reaction kinetics of the dimerization of some polyhalogenated allenes with the general formula Cl2CCCCIX (X = Cl, Br, C6H5, COOEt) and of tetrabromoallene was studied by an IR spectrophotometric method. The reaction was found to be of strictly second order kinetics. The activation parameters were determined and the experimental data and the influence of the substituents were discussed in terms of the accepted general theory of allene cycloaddition. All data are in agreement with a non-concerted two-step electrocyclic addition mechanism. Within the experimental limits no paramagnetic species like a diradical could be detected by the ESR-method during the dimerization re…

DiradicalAlleneOrganic ChemistryPhotochemistryBiochemistryCycloadditionChemical kineticschemistry.chemical_compoundParamagnetismMonomerchemistryGeneral theoryComputational chemistryThermal instabilityDrug DiscoveryTetrahedron
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Path-wise versus kinetic modeling for equilibrating non-Langevin jump-type processes

2014

We discuss two independent methods of solution of a master equation whose biased jump transition rates account for long jumps of L\'{e}vy-stable type and nonetheless admit a Boltzmannian (thermal) equilibrium to arise in the large time asymptotics of a probability density function $\rho (x,t)$. Our main goal is to demonstrate a compatibility of a {\it direct} solution method (an explicit, albeit numerically assisted, integration of the master equation) with an {\it indirect} path-wise procedure, recently proposed in [Physica {\bf A 392}, 3485, (2013)] as a valid tool for a dynamical analysis of non-Langevin jump-type processes. The path-wise method heavily relies on an accumulation of large…

Direct solution methodStatistical Mechanics (cond-mat.stat-mech)PhysicsQC1-999cauchy driverGeneral Physics and AstronomyFOS: Physical sciencesmaster equationProbability density functionlévy processesKinetic energynon-langevin modellinggillespie’s algorithmLévy processboltzmann equilibriumThermalMaster equationJumpStatistical analysisStatistical physicsCondensed Matter - Statistical Mechanicspath-wise modellingMathematics
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