Search results for " kinetic"

showing 10 items of 416 documents

Crystallization kinetics of amorphous SiC films: Influence of substrate

2005

Abstract The crystallization kinetics of amorphous silicon carbide films was studied by means of X-ray diffractometry (XRD) and transmission electron microscopy (TEM). The films were deposited by radio frequency (r.f.) magnetron sputtering on glassy carbon and single crystalline silicon substrates, respectively. TEM micrographs and XRD patterns show the formation of nano-crystalline β-SiC with crystallite sizes in the order of 50 nm during annealing at temperatures between 1200 and 1600 °C. A modified Johnson–Mehl–Avrami–Kolmogorov (JMAK) formalism was used to describe the isothermal transformation of amorphous SiC into β-SiC as an interface controlled, three-dimensional growth processes fr…

Amorphous siliconMaterials scienceSiliconGeneral Physics and Astronomychemistry.chemical_elementGlassy carbonlaw.inventionchemistry.chemical_compoundsilicon carbidelawcrystallization kineticsCrystalline siliconCrystallizationsputter depositionSurfaces and InterfacesGeneral ChemistrySputter depositionCondensed Matter PhysicsSurfaces Coatings and FilmsAmorphous solidamorphous filmsCrystallographychemistryChemical engineering[ CHIM.MATE ] Chemical Sciences/Material chemistryCrystalliteApplied Surface Science
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Hybrid TiO2 @ phthalocyanine catalysts in photooxidation of 4-nitrophenol: Effect of the matrix and sensitizer type

2020

Abstract Microcrystalline and nanocrystalline anatase (TiO2) based hybrid photocatalysts including selected phthalocyanine sensitizers were explored in photooxidation of 4-nitrophenol (4-NP) in water. Composites obtained with the homemade pure nano-anatase displayed a very poor catalytic performance compared to the other ones prepared from the commercial Tioxide-Huntsman (micro) and Evonik P25 (nano) products. In particular, the microcrystalline anatase impregnated with sandwich phthalocyanines of Gd or Yb showed excellent results both in photooxidation of 4-NP and hydroquinone, and proved the only ones which completely removed these two compounds from the system during the same reaction cy…

AnataseGeneral Chemical EngineeringHydroquinoneGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural sciences4-nitrophenolCatalysisChemical kineticsReaction ratechemistry.chemical_compoundMetallophthalocyaninesLanthanideLanthanidesHybrid photocatalystHydroquinoneChemistry4-NitrophenolGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMicrocrystallineChemical engineeringPhthalocyanineTitanium dioxideMetallophthalocyanine0210 nano-technologyHybrid photocatalystsJournal of Photochemistry and Photobiology A: Chemistry
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Influence of pH on the degradation kinetics of nitrophenol isomers in a heterogeneous photocatalytic system

1993

Abstract The kinetics of photocatalytic degradation of 2-, 3- and 4-nitrophenol in aqueousdispersions containing TiO2 (anatase) has been investigated at different initial values of pH and concentrations of substrate. A pseudo-first order kinetics with respect to the nitrophenol concentration was found to hold; an increase of the substrate concentration and the initial pH was detrimental on the degradation rate.

AnataseNitrophenolchemistry.chemical_compoundDegradation kineticsChemistryProcess Chemistry and TechnologyKineticsInorganic chemistryPhotocatalysisSubstrate (chemistry)Degradation (geology)CatalysisCatalysisApplied Catalysis A: General
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Tin(IV) catalyzed D-galacturonic acid anomerization

2008

A comparative kinetic study of anomerization between the four main forms (alpha/beta-pyranosides and alpha/beta-furanosides) of D-galacturonic acid (GalAH(2), 1) and tin(IV) complexed D-galacturonate ([Sn(CH(3))(2)(GalA)(H(2)O)(2)], 2) in D(2)O, is reported. Important differences are shown by pD vs. mutarotation rate profiles of 1 and 2. Coordination, in fact, causes: i) a spectacular increase of the rate due to kinetic template assistance of the carboxylic tail holding the metal in close proximity to the reactive centre and ii) a change in the dependence of the rate on the pD. Entropic and enthalpic factors contribute to the huge activation energy decrease in 2. Anomerization rates of the …

AnomerMagnetic Resonance SpectroscopyRotationStereochemistrychemistry.chemical_elementMedicinal chemistryMutarotationCatalysisCatalysiskinetic template effectInorganic Chemistrychemistry.chemical_compoundReaction rate constantNMR spectroscopyNucleophilegalacturonic acidanomerizationTin(IV)/ NMR kinetic / Galacturonic / 119SnHexuronic AcidsTin CompoundsStereoisomerismRing sizeKineticschemistryNMR spectroscopy; kinetic template effect; galacturonic acid; Tin(IV) catalysis; anomerizationTinTin(IV) catalysisD-Galacturonic acid
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Modelagem da cinética de secagem de discos de maçã e abobrinha impregnadas a vácuo com antocianinas

2019

ABSTRACT: The aim of this research was to study the drying kinetics of apple and zucchini slices enriched with anthocyanins and to evaluate the influence of drying temperature on the anthocyanin content of apple and zucchini snacks. Apple (Granny Smith) and zucchini (Cucurbita pepo) slices were enriched with anthocyanins by vacuum impregnation with blueberry juice. Then, slices were dehydrated at 40, 50 and 60 ºC with 1.0 m/s air flow. Dehydrated samples were referred to as anthocyanin enriched snacks. Diffusion coefficient values improved by increasing the drying temperature, within the 2.81×10-10 to 5.78×10-10 m2/s range for apple slices and 2.02×10-10 to 3.99×10-10 m2/s for zucchini slic…

AnthocyaninFunctional snackDrying kineticcinética de secagemfunctional snackslcsh:AgricultureCucurbita pepochemistry.chemical_compoundAir dryingmodelagem matemáticalcsh:Agriculture (General)drying kineticsGeneral VeterinarybiologyChemistry0402 animal and dairy sciencemathematical modelinglcsh:S04 agricultural and veterinary sciencesbiology.organism_classification040201 dairy & animal scienceanthocyaninslcsh:S1-972Horticulturesnacks funcionaisAnthocyanin040103 agronomy & agriculture0401 agriculture forestry and fisheriesMathematical modelingAnimal Science and ZoologyantocianinasTecnologia dels alimentsAgronomy and Crop ScienceCiência Rural
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Betacyanins as phenol antioxidants. Chemistry and mechanistic aspects of the lipoperoxyl radical-scavenging activity in solution and liposomes.

2009

Reaction kinetics of betanin and its aglycone betanidin towards peroxyl radicals generated from the azo-initiated oxidation of methyl linoleate in methanol, and of a heterogeneous aqueous/soybean phosphatidylcholine liposomal system, were studied by monitoring formation of linoleic acid hydroperoxides and consumption of the pigments. Betanin was a weak retarder in methanol, and an effective chain breaking antioxidant in the liposomal model, indicating that kinetic solvent effects and partition in lipid bilayers may affect its activity. Betanidin behaved as a chain terminating antioxidant in both models. Kinetic parameters characterizing peroxyl radical-scavenging activity showed that betani…

Antioxidantmedicine.medical_treatmentLipid Bilayersalpha-TocopherolBiochemistryChemical kineticsLinoleic Acidchemistry.chemical_compoundStructure-Activity RelationshipReaction rate constantSettore BIO/10 - BiochimicamedicineBetacyaninsOrganic chemistryChromatography High Pressure LiquidBetaninAqueous solutionMolecular StructureMethanolWaterDrug SynergismGeneral MedicineFree Radical ScavengersSolutionsAglyconechemistryLinoleic Acidsbetacyanins betanin betanidin lipid peroxides liposomes antioxidant phytochemicalsSpectrophotometryLiposomesPhosphatidylcholinesSolventsMethanolBetacyaninsLipid PeroxidationOxidation-ReductionFree radical research
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A study on the essential oil Ferulago campestris. How much does exstraction method influence the oil composition?

2010

The essential oil of different parts of Ferulago campestris (Bess.) collected in Sicily has been extracted by microwave-assisted hydrodistillation (MAHD) and by classic hydrodistillation (HD). A comparative qualitative- quantitative study on the composition of the oils was carried out. A total of 100 compounds were identified in the oils obtained by MAHD, whereas 88 compounds characterized the HD oils. The most prominent components were, in all different parts of F. campestris and in both extraction methods, 2,4,5- trimethylbenzaldehyde and 2,4,6-trimethylbenzaldehyde isomers; the latter was not previously found. The attempt to evaluate where the oil components are located in all parts of t…

Apiaceae / Essential oils / Ferulago campestris / Kinetic of microwave extraction / Microwaves hydrodistillationIsomerismKinetic of microwave extractionMicrowaves hydrodistillationOils VolatilePlant OilsSettore CHIM/06 - Chimica OrganicaMicrowavesEssential oilDistillationApiaceaeFerulago campestri
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Masstodon : a tool for assigning peaks and modeling electron transfer reactions in top-down mass spectrometry

2019

Abstract: Top-down mass spectrometry methods are becoming continuously more popular in the effort to describe the proteome. They rely on the fragmentation of intact protein ions inside the mass spectrometer. Among the existing fragmentation methods, electron transfer dissociation is known for its precision and wide coverage of different cleavage sites. However, several side reactions can occur under electron transfer dissociation (ETD) conditions, including nondissociative electron transfer and proton transfer reaction. Evaluating their extent can provide more insight into reaction kinetics as well as instrument operation. Furthermore, preferential formation of certain reaction products can…

Apolipoprotein A-IUbiquitinChemistry010401 analytical chemistryElectronsSubstance PTracing010402 general chemistryMass spectrometry01 natural sciencesMass Spectrometry0104 chemical sciencesAnalytical ChemistryIonElectron-transfer dissociationChemical kineticsElectron transferChemistryFragmentation (mass spectrometry)Chemical physicsMass spectrumAlgorithmsSoftwareAnalytical chemistry
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Photocatalytic activity of transition-metal-loaded titanium(IV) oxide powders suspended in aqueous solutions: Correlation with electron–hole recombin…

2001

Photocatalytic reactions by transition-metal (V, Cr, Fe, Co, Cu, Mo, or W) loaded TiO2 (M-TiO2) powders suspended in aqueous solutions of methanol, (S)-lysine (Lys), or acetic acid were investigated. The photoactivities of various samples were compared with the rate constant (kr) of recombination of photoexcited electrons and positive holes determined by femtosecond pump–probe diffuse reflection spectroscopy (PP-DRS). As a general trend, increased loading decreased the rate of formation of the main products (H2 , pipecolinic acid (PCA), and CO2) under UV (>300 nm) irradiation, and the effect became more intense on increasing the loading. In PP-DRS, these M-TiO2 gave similar decays of absorp…

Aqueous solutionChemistryStereochemistryKineticsAnalytical chemistryOxideGeneral Physics and AstronomyChemical kineticschemistry.chemical_compoundReaction rate constantTransition metalPhotocatalysisPhysical and Theoretical ChemistryAbsorption (chemistry)Physical Chemistry Chemical Physics
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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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