Search results for "kinetics"

showing 10 items of 2224 documents

Periodic behaviour in heterogeneous chemical reactions

1992

Abstract The authors present an analytical and numerical analysis for a solid-gas oxidation process represented by a set of coupled reaction rates equations. The equations describe the time evolution of four elementary process that govern the overall heterogeneous kinetics. The description formation of a new oxide unit considers: (1) an internal interface (oxide-metal) reaction by which an activated complex is formed; (2) the dissolution of the complex produce a chemical element σ; (3) the diffusion of σ through the oxide layer; and (4) an external interface (oxide-gas) reaction. The results reported here delinate the parameter region where chemical oscillations are present.

ChemistryActivated complexNumerical analysisKineticsTime evolutionOxideThermodynamicsGeneral ChemistryCondensed Matter PhysicsChemical reactionchemistry.chemical_compoundPhysical chemistryGeneral Materials ScienceDiffusion (business)DissolutionSolid State Ionics
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Energy landscapes of ligand-receptor couples probed by dynamic force spectroscopy.

2013

Playing a dominant role in many biochemical processes are the dynamic properties of molecular linkages; examples include cell adhesion, enzyme-catalyzed reactions, and molecular recognition by antibodies. Dynamic force spectroscopy, namely separating molecular bonds under external force ramps has rapidly become a powerful tool to study the rugged energy landscape of noncovalent ligand-receptor bonds. The picture shows a surface and tip-bound pair being pulled apart and the derived potential energy diagram.

ChemistryAnalytical chemistryEnergy landscapeProteinsLigand (biochemistry)LigandsMicroscopy Atomic ForcePotential energyAtomic and Molecular Physics and OpticsDynamic force spectroscopyKineticsMolecular recognitionChemical physicsCovalent bondPhysical and Theoretical ChemistryEnergy (signal processing)Protein BindingChemphyschem : a European journal of chemical physics and physical chemistry
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Anomalous Kinetics of Diffusion-Controlled Defect Annealing in Irradiated Ionic Solids

2017

The authors thanks A. Ch. Lushchik, M. Izerrouken, and V. Lisitsyn for stimulating discussions. This work has been carried out within the framework of the EUROfusion Consortium and has received funding from the Euroatom research and training programme 2014-2018 under Grant Agreement No. 633053. The views and opinions expressed herein do not necessarily reflect those of the European Commission. R.V. acknowledges the financial support by the MEIC (Ministerio de Economa, Industria y Competitivad; Project ENE2015-70300-C3-1-R). The calculations were performed using facilities of the Stuttgart Supercomputer Center (Project DEFTD 12939).

ChemistryAnnealing (metallurgy)KineticsIonic bonding02 engineering and technologyElectronRadiation021001 nanoscience & nanotechnology01 natural sciences7. Clean energyFluenceMolecular physicsIon0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]IrradiationPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyThe Journal of Physical Chemistry A
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Kinetics of styrene biodegradation by Pseudomonas sp. E-93486

2011

The research into kinetics of styrene biodegradation by bacterial strain Pseudomonas sp. E-93486 coming from VTT Culture Collection (Finland) was presented in this work. Microbial growth tests in the presence of styrene as the sole carbon and energy source were performed both in batch and continuous cultures. Batch experiments were conducted for initial concentration of styrene in the liquid phase changed in the range of 5–90 g m−3. The Haldane model was found to be the best to fit the kinetic data, and the estimated constants of the equation were: μm = 0.1188 h−1, KS = 5.984 mg l−1, and Ki = 156.6 mg l−1. The yield coefficient mean value \documentclass[12pt]{minimal} \usepackage{amsmath} \…

ChemistryBatch experimentKineticsAnalytical chemistryGeneral MedicineChemostatBacterial growthApplied Microbiology and BiotechnologyBiotechnological Products and Process EngineeringCarbonDilutionStyreneKineticschemistry.chemical_compoundChemostatPseudomonasYield (chemistry)Organic chemistrySensitivity (control systems)Energy sourceStyreneBiotransformationBiotechnologyApplied Microbiology and Biotechnology
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Chaotic dynamics in an unstirred ferroin catalyzed Belousov–Zhabotinsky reaction

2009

Abstract The Belousov–Zhabotinsky (BZ) reaction is the best known example of far from equilibrium self-organizing chemical reaction. Among the many dynamical behaviors that this reaction can exhibit, spatio-temporal chaos attracted particular interest, both for the ferroin and cerium catalyzed systems. In recent years transient chaos was found in the cerium catalyzed BZ reaction, when conducted in batch and unstirred reactors. It was established that the chaotic oscillations, originated by the coupling among chemical kinetics and transport phenomena, appeared and disappeared following a Ruelle–Takens–Newhouse scenario. In this Letter, we show results about the ferroin catalyzed system condu…

ChemistryChaoticGeneral Physics and Astronomychemistry.chemical_elementChemical reactionCatalysisChemical kineticsCeriumchemistry.chemical_compoundBelousov–Zhabotinsky reactionChemical physicsFerroinPhysical chemistryBelousov–Zhabotinsky spatiotemporal chaos ferroinPhysical and Theoretical ChemistryTransport phenomenaSettore CHIM/02 - Chimica FisicaChemical Physics Letters
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Mechanistic and kinetic insight into spontaneous cocrystallisation of isoniazid and benzoic acid

2015

Solid-state cocrystallisation is of contemporary interest, because it offers an easy and efficient way to produce cocrystals, which are recognized as prospective pharmaceutical materials. Research explaining solid-state cocrystallisation mechanisms is important, but still too scarce to give a broad understanding of factors governing and limiting these reactions. Here we report an investigation of the mechanism and kinetics of isoniazid cocrystallisation with benzoic acid. This reaction is spontaneous; however its rate is greatly influenced by environmental conditions (humidity and temperature) and pre-treatment (milling) of the sample. The acceleration of cocrystallisation in the presence o…

ChemistryChemistry PharmaceuticalIsoniazidKineticsPharmaceutical Sciencefood and beveragesLimitingBenzoic AcidCocrystalKineticschemistry.chemical_compoundDrug StabilitySolubilityX-Ray DiffractionMechanism (philosophy)MechanochemistryDrug DiscoveryIsoniazidmedicineThermodynamicsMolecular MedicineOrganic chemistryCrystallizationmedicine.drugBenzoic acid
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Electrodeposition methods in superheavy element chemistry

2008

To prepare electrodeposition experiments with superheavy elements (SHE), their homologs were investigated. In the experiments, various electrode materials and electrolytes were used. Critical potentials (E crit ) where the electrodeposition starts and potentials for the deposition of 50% of the atoms in solution (E 50% ) were determined. Underpotential deposition was observed in most cases. An electrolytic cell for a fast electrochemical deposition was developed and the time for the deposition of 50% of the atoms in solution (t 50% ) was determined. Short lived α-emitting isotopes were produced at Gesellschaft fur Schwerionenforschung (GSI), Darmstadt, transferred to the aqueous phase with …

ChemistryElectrolytic cellInorganic chemistryKineticsAqueous two-phase systemCoupling (piping)ElectrolytePhysical and Theoretical ChemistryElectrochemistryUnderpotential depositionDeposition (chemistry)Radiochimica Acta
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Convective mass transfer to partially recessed and porous electrodes

2003

Abstract The diffusional problem of a rotating porous electrode has been analysed based on the mass transfer equations for a partially blocked electrode. It is shown that the porous geometry leads to a dependence of the current on rotation rate identical to that corresponding to a coupled diffusion-activated electron transfer mechanism. The apparent rate constant, however, is related only to the geometry of the porous surface. It is shown that the characteristic diffusional length corresponds to the pore dimension modified by a term including the transition from linear to spherical diffusional geometry at the pore entrance. The theory is compared with experimental results for the reduction …

ChemistryGeneral Chemical EngineeringAnalytical chemistryElectrochemical kineticsThermodynamicsTortuosityAnalytical ChemistryElectron transferMass transferElectrodeElectrochemistryRotating disk electrodePorosityElectrode potentialJournal of Electroanalytical Chemistry
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Asymmetric Hydrogenation of Nonfunctionalized Olefins in Propylene Carbonate—Kinetic or Thermodynamic Control?

2011

Iridium-catalyzed hydrogenations of nonfunctionalized olefins in propylene carbonate as the solvent allow efficient catalysis with much higher enantioselectivities in comparison with dichloromethane which is usually employed for these reactions. Experimental and computational studies of the hydrogenation of 1-methylene-1,2,3,4-tetrahydronaphthalene have been performed to understand the limitation for this reaction.

ChemistryGeneral Chemical EngineeringKineticsInorganic chemistryAsymmetric hydrogenationGeneral ChemistryKinetic energyIndustrial and Manufacturing EngineeringCatalysisSolventchemistry.chemical_compoundPropylene carbonateOrganic chemistryDichloromethaneIndustrial & Engineering Chemistry Research
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Porous materials as delivery and protective agents for Vitamin A

2016

The suitability of porous materials to immobilize and release under control bioactive molecules prompted us to design and study delivery systems of Vitamin A (VitA). This molecule, relevant in several physiological functions, is easily oxidized. Commercial VitA was immobilized in two different clays, montmorillonite K-10 (MMT) and sepiolite (SEP), and in MCM-41, by impregnation. Characterization of the resulting hybrid materials by XRD, FTIR and 13C and 29Si (MAS) NMR spectroscopies revealed its presence. The photo-stability tests showed decreased degradation of VitA in the clays, compared to MCM-41 and the pure VitA, while thermostability is observed until ∼100 °C. The kinetics of the rele…

ChemistryGeneral Chemical EngineeringSepioliteKinetics020101 civil engineering02 engineering and technologyGeneral Chemistry021001 nanoscience & nanotechnologyControlled release0201 civil engineeringchemistry.chemical_compoundMontmorilloniteOrganic chemistryDegradation (geology)Fourier transform infrared spectroscopy0210 nano-technologyHybrid materialNuclear chemistryThermostabilityRSC Advances
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