Search results for "Reaction kinetic"

showing 10 items of 21 documents

Zero-field nuclear magnetic resonance of chemically exchanging systems.

2019

Zero- to ultralow-field (ZULF) nuclear magnetic resonance (NMR) is an emerging tool for precision chemical analysis. In this work, we study dynamic processes and investigate the influence of chemical exchange on ZULF NMR J-spectra. We develop a computational approach that allows quantitative calculation of J-spectra in the presence of chemical exchange and apply it to study aqueous solutions of [15N]ammonium (15N\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${\mathrm{H}}_4^ +$$\end{document}H4+) as a model syst…

0301 basic medicineReaction kinetics and dynamicsSciencePhysics::Medical PhysicsGeneral Physics and AstronomyModel system02 engineering and technologyGeneral Biochemistry Genetics and Molecular BiologyArticle03 medical and health sciencesNuclear magnetic resonanceZero fieldHyperpolarization (physics)lcsh:ScienceDissolutionQuantitative Biology::Biomolecules3403 Macromolecular and Materials ChemistryMultidisciplinaryAqueous solution34 Chemical SciencesChemical exchangeQ500Diagnostic markersGeneral ChemistryNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnologyequipment and supplies030104 developmental biologylcsh:Qddc:5000210 nano-technologyhuman activitiesSolution-state NMR51 Physical Sciences
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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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Oligomerization and hemolytic properties of the C-terminal domain of pyolysin, a cholesterol-dependent cytolysin

2013

Pyolysin (PLO) belongs to the homologous family of the cholesterol- dependent cytolysins (CDCs), which bind to cell membranes containing cholesterol to form oligomeric pores of large size. The CDC monomer structure consists of 4 domains. Among these, the C-terminal domain 4 has been implicated in membrane binding of the monomer, while the subsequent processes of oligomerization and membrane insertion have primarily been assigned to other domains of the molecule. Recombinantly expressed or proteolytic fragments that span domain 4 of the CDCs streptolysin O and perfringolysin O bind to membranes but fail to oligomerize, and they inhibit the activity of the respective wild-type toxins. We repo…

ErythrocytesMembrane bindingCellprotein bindingBiochemistryoligomerHemolysin Proteinschemistry.chemical_compoundReaction kineticsToxic materialsMonomersprotein domainRecombinant ProteinsHemolysisunclassified drugcytolysinmedicine.anatomical_structureMembraneBiochemistryStreptolysinsStreptolysinLarge sizeBacterial ToxinsBiologyCholesterol-dependent cytolysinHemolysisoligomerizationMembrane LipidsBacterial ProteinsProteolytic fragmentsEscherichia colimedicineAnimalsMonomer structuresMolecular BiologySheep Domesticcarboxy terminal sequenceC-terminal domainsCholesterolC-terminusCell MembraneHemolytic activitycholesterolCell Biologymedicine.diseaseProtein Structure TertiaryCell membranesKineticschemistryOligomersProtein MultimerizationPyolysinprotein pyolysinMembrane insertionCytology
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Transesterification of rapeseed oil over acid resins promoted by supercritical carbon dioxide

2011

The methanolysis of rapeseed oil catalyzed by commercial styrene-divinylbenzene macroporous acid resins was performed in a batch reactor at 100-140 °C and 10-46 MPa to study the effect of supercritical carbon dioxide (scCO2) on the performances of the process. Reaction temperatures of 120-140 °C were necessary to obtain high enough yields of fatty acid methyl esters. Upon addition of scCO2 faster transesterification kinetics was obtained also at the lowest investigated operating pressure (10-11 MPa), working in two fluid phase systems. Experiments performed changing the reaction time indicated that most of the esters were formed during the first 3 h. When the pressure was increased at 38-46…

General Chemical EngineeringMethanolysiKineticsBatch reactorOperating pressurePolymeric acidHeterogeneous catalysisCatalysiCatalysisHeterogeneous catalysiIon exchange resinSupercritical carbon dioxideOrganic chemistryFatty acid methyl esterRapeseed oilEsterPhysical and Theoretical ChemistryVegetable oils Supercritical fluid extractionIon-exchange resinStyreneReaction systemReaction timeBiodieselFluid phasiTwo-fluid Batch reactorSupercritical carbon dioxideEsterificationChemistryReaction kineticTransesterificationSettore ING-IND/27 - Chimica Industriale E TecnologicaFatty acidCondensed Matter PhysicsPhase behaviourTransesterificationCarbon dioxideReaction temperatureMacroporouStyrene-divinylbenzeneBiodieselEnhancement effectIon exchangeThe Journal of Supercritical Fluids
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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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Development of a modular room-temperature hydride storage system for vehicular applications

2016

The subject of this paper concerns the development of a vehicular hydrogen tank system, using a commercial interstitial metal hydride as storage material. The design of the tank was intended to feed a fuel cell in a light prototype vehicle, and the chosen hydride material, Hydralloy C5 by GfE, was expected to be able to absorb and desorb hydrogen in a range of pressure suitable for this purpose. A systematic analysis of the material in laboratory scale allows an extrapolation of the thermodynamic and reaction kinetics data. The following development of the modular tank was done according to the requirements of the prototype vehicle propulsion system and led to promising intermediate results…

Interstitial metalComputer sciencePrototype vehicle02 engineering and technologyPropulsionHydrogen tankPropulsion010402 general chemistry01 natural sciencesHydrogen storageSorption proceRange (aeronautics)General Materials ScienceProcess engineeringFlexibility (engineering)Hydridebusiness.industryHydrideFuel cellVehicular applicationsReaction kineticGeneral ChemistryModular designHydrogen storage021001 nanoscience & nanotechnology0104 chemical sciencesTanks (containers)Computer data storageModular approach0210 nano-technologybusinessHeat management
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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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Dynamic Effects on Reaction Rates in a Michael Addition Catalyzed by Chalcone Isomerase. Beyond the Frozen Environment Approach

2008

We present a detailed microscopic study of the dynamics of the Michael addition reaction leading from 6'-deoxychalcone to the corresponding flavanone. The reaction dynamics are analyzed for both the uncatalyzed reaction in aqueous solution and the reaction catalyzed by Chalcone Isomerase. By means of rare event simulations of trajectories started at the transition state, we have computed the transmission coefficients, obtaining 0.76 +/- 0.04 and 0.87 +/- 0.03, in water and in the enzyme, respectively. According to these simulations, the Michael addition can be seen as a formation of a new intramolecular carbon-oxygen bond accompanied by a charge transfer essentially taking place from the nu…

Models MolecularReaction ratesMechanicsBiochemistryChemical reactionCatalysisReaction coordinateReaction rateMolecular dynamicsCharge transferChalconesColloid and Surface ChemistryNucleophileComputational chemistryChemical reactionsFreezingIntramolecular LyasesReaction kineticsFourier AnalysisChemistryIntermolecular forceWaterGeneral ChemistryCarbonDynamicsKineticsModels ChemicalReaction dynamicsChemical physicsIntramolecular forceFlavanonesQuantum TheoryThermodynamicsIon exchangeJournal of the American Chemical Society
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