Search results for " Reaction kinetic"

showing 7 items of 7 documents

Importance of the liquid to solid weight ratio in the powdered solid-liquid reactions Example drawn from cement constituent hydration

1997

Abstract It seems justified to wonder if the chemical processes which have been evidenced from diluted stirred suspensions are or are not in accordance with those involved in a stagnant paste. The present paper is aimed at clarifying this question which is in connection with the problem of the so called ‘dormant period’ or ‘induction period’ at the beginning of the hydration of Portland cement.

CementChemistryInduction periodMineralogyGeneral ChemistryCondensed Matter PhysicsSuspension (chemistry)law.inventionPortland cementChemical reaction kineticsChemical engineeringlawSpecific surface areaGeneral Materials ScienceSolid liquidSolid State Ionics
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Hydration of cementitious materials, present and future

2011

This paper is a keynote presentation from the 13th International Congress on the Chemistry of Cement. It discusses the underlying principles of hydration and recent evidence for the mechanisms governing this process in both Portland cements and other cementitious materials. Given the overriding imperative to improve the sustainability of cementitious materials, routes to reducing CO2 emissions are discussed and the impact of supplementary materials on hydration considered. (C) 2011 Elsevier Ltd. All rights reserved.

CementWaste managementChemistry0211 other engineering and technologies02 engineering and technologyBuilding and Construction021001 nanoscience & nanotechnologylaw.inventionchemistry.chemical_compoundPortland cementChemical reaction kinetics13. Climate actionlawInternational congress021105 building & constructionForensic engineeringGeneral Materials ScienceCementitiousCalcium silicate hydrate0210 nano-technologyTricalcium silicateCement and Concrete Research
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Application of model quality evaluation to systems biology

2008

Application of model quality evaluation to the quasispecies models is presented. These models are useful for the analysis of the DNA and RNA evolution and for the description of the population dynamics of viruses and bacteria. An estimate of the parameters together with their interval of variability is computed and the quality evaluation is tested on the basis of the model prediction error capability.

Computer sciencemedia_common.quotation_subjectSystems biologyset membershipPopulationViral quasispeciesInterval (mathematics)Computational biologycomputer.software_genreSettore ING-INF/04 - AutomaticaModels of DNA evolutionmolecular biophysicsQuality (business)educationgenetics microorganismsmedia_commoneducation.field_of_studyDNA; biochemistry evolution (biological); genetics microorganisms; molecular biophysics; reaction kinetics; identification; set membership; optimizationBasis (linear algebra)Estimation theoryDNADNA biochemistry evolution (biological) genetics microorganisms molecular biophysics reaction kinetics identification set membership optimizationbiochemistry evolution (biological)identificationreaction kineticsData miningcomputeroptimization
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Molecular dynamics simulations of elementary chemical processes in liquid water using combined density functional and molecular mechanics potentials.…

1997

The first molecular dynamics (MD) simulation of a chemical process in solution with an ab initio description of the reactant species and a classical representation of the solvent is presented. We study the dynamics of proton (deuterium) transfer in strongly hydrogen-bonded systems characterized by an energy surface presenting a double well separated by a low activation barrier. We have chosen the hydroxyl-water complex in liquid water to analyze the coupling between the reactive system and the environment. The proton is transferred from one well to the other with a frequency close to 1 ps−1 which is comparable to the low-frequency band associated to hindered translations, diffusional transl…

Hydrogen bonds ; Molecular dynamics method ; Ab initio calculations Ion exchange ; Solvent effects ; Reaction kinetics theory ; Density functional theory ; Intermolecular mechanicsProtonChemistryGeneral Physics and AstronomyIntermolecular mechanicsMolecular dynamics methodHydrogen bondsUNESCO::FÍSICA::Química físicaMolecular dynamicsAb initio calculations Ion exchangeDeuteriumReaction dynamicsChemical physicsComputational chemistryAb initio quantum chemistry methodsSolvent effectsReaction kinetics theoryDensity functional theoryDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsChemical equilibrium:FÍSICA::Química física [UNESCO]
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A theoretical insight into the photophysics of psoralen

2006

Psoralen photophysics has been studied on quantum chemistry grounds using the multiconfigurational second-order perturbation method CASPT2. Absorption and emission spectra of the system have been rationalized by computing the energies and properties of the low-lying singlet and triplet excited states. The S1 ππ* state has been determined to be responsible of the lowest absorption and fluorescence bands and to initially carry the population in the photophysical processes related to the phototherapeutic properties of psoralen derivatives. The low-lying T1 ππ* state is, on the other hand, protagonist of the phosphorescence, and its prevalent role in the reactivity of psoralen is suggested to b…

LightPhotochemistryPopulationMolecular ConformationGeneral Physics and AstronomyPerturbation theoryPhotochemistryQuantum chemistryFluorescenceAbsorptionElectromagnetic FieldsTriplet state Excited statesOrganic compoundsReaction kinetics theoryEmission spectrumSinglet statePhysical and Theoretical ChemistryPerturbation theoryTriplet stateeducation:FÍSICA::Química física [UNESCO]education.field_of_studyMolecular StructureChemistryChemistry PhysicalPhosphorescenceFicusinModels TheoreticalCarbonUNESCO::FÍSICA::Química físicaSpectrometry FluorescenceModels ChemicalOrganic compounds ; Photochemistry ; Perturbation theory ; Reaction kinetics theory ; Fluorescence ; Phosphorescence ; Triplet state Excited statesExcited stateQuantum TheoryPhosphorescenceSoftware
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Structural, energetic and kinetic database of catalytic reactions: Benzyl alcohol to benzaldehyde oxidation on MnOx clusters

2021

Abstract Data here reported are connected with the research article “Benzyl Alcohol to Benzaldehyde Oxidation on MnO x Clusters: Unraveling Atomistic Features” Gueci et al. [1] . This work described and discussed structural and energetic results, calculated by Density Functional Theory (DFT). In order to get kinetic information, DFT results were refined by an original approach, which will be shortly described in the following article. The crossed analysis of experimental and computational energetic and kinetic data allowed to (i) reconstruct the complicated lattice that connects the primary and secondary mechanisms of the reaction and (ii) identify alternative process pathways capable of by…

Work (thermodynamics)Science (General)MultidisciplinaryMaterials scienceMnOx Oxidative–dehydrogenation Deactivation Remediation DFT Reaction kineticMnOxComputer applications to medicine. Medical informaticsKineticsDeactivationReaction kineticR858-859.7RemediationAlternative processHeterogeneous catalysisDFTCatalysisBenzaldehydeQ1-390chemistry.chemical_compoundchemistryBenzyl alcoholComputational chemistryDensity functional theoryOxidative–dehydrogenationSettore CHIM/02 - Chimica FisicaData in Brief
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Investigation of Multicomponent Sorption in Polymers from Fluid Mixtures at Supercritical Conditions:  The Case of the Carbon Dioxide/Vinylidenefluor…

2008

The simultaneous sorption of carbon dioxide and vinylidene fluoride (VDF) in poly(vinylidenefluoride) from their supercritical (sc) mixtures was studied using an experimental method, already described in a previous publication, based on the gas-chromatographic determination of the equilibrium composition of the fluid phase in contact with the polymer. Argon was added to the system as a nonabsorbable molecular probe in the polymer to take into account the effect of the volume swelling on the measurement. Sorption behavior has been studied at 50 °C by changing the composition and the density of the supercritical phase. We have found that VDF dissolves in its polymer with concentrations much l…

chemistry.chemical_classificationSettore ING-IND/26 - Teoria Dello Sviluppo Dei Processi ChimiciPolymers and PlasticsOrganic ChemistryRadical polymerizationSorptionPolymerSettore ING-IND/27 - Chimica Industriale E TecnologicaSupercritical fluidInorganic Chemistrychemistry.chemical_compoundChemical reaction kineticsMonomerchemistryChemical engineeringCarbon dioxideMaterials ChemistryOrganic chemistryFluorideFluid mechanicsGas chromatographyPolymerizationPolymersSorptionMacromolecules
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