Search results for "calor"

showing 10 items of 866 documents

Understanding the Solution Behavior of Epinephrine in the Presence of Toxic Cations: A Thermodynamic Investigation in Different Experimental Conditio…

2020

The interactions of epinephrine ((R)-(&minus

EnthalpyInorganic chemistryPharmaceutical ScienceIonic bondingProtonation02 engineering and technologyCalorimetry010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug Discoverytoxic cationSettore CHIM/01 - Chimica Analiticatoxic cationsepinephrinePhysical and Theoretical ChemistryChemistryOrganic Chemistryenthalpy and entropy changesOxidesMethylmercury Compoundsdependence on ionic strength021001 nanoscience & nanotechnologysequestering ability0104 chemical sciencesSpecific ion interaction theoryChemistry (miscellaneous)Ionic strengthBenzyl alcoholThermodynamicsUraniumMolecular MedicineTitration0210 nano-technologyenthalpy and entropy changeMolecules
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Sorption Equilibria of Ethanol on Cork

2013

International audience; We report here for the first time a thermodynamic study of gaseous ethanol sorption on raw cork powder and plate. Our study aims at a better understanding of the reactivity of this material when used as a stopper under enological conditions, thus in close contact with a hydroethanolic solution, wine. Sorption−desorption isotherms were accurately measured by thermogravimetry at 298 K in a large range of relative pressures. Sorption enthalpies were determined by calorimetry as a function of loading. Sorption−desorption isotherms exhibit a hysteresis loop probably due to the swelling of the material and the absorption of ethanol. Surprisingly, the sorption enthalpy of e…

EnthalpyWine02 engineering and technologyCalorimetryCorkengineering.materialCalorimetry010402 general chemistrycomplex mixtures01 natural sciencesEndothermic processPermeabilityQuercusMaterials TestingmedicineOrganic chemistry[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyChemistryFood PackagingSorptionGeneral Chemistry021001 nanoscience & nanotechnologyWood0104 chemical sciencesThermogravimetryKineticsModels ChemicalChemical engineeringSulfur dioxide13. Climate actionengineeringSorptionAdsorptionethanolAbsorption (chemistry)Swellingmedicine.symptom0210 nano-technologyGeneral Agricultural and Biological SciencesCork
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Evaluation of entropies of fusion of polychlorinated naphthalenes by model congeners: A DSC study

2006

Abstract Thirteen congeners of polychlorinated naphthalenes (PCN) were synthesized and studied by differential scanning calorimetry (DSC). Melting points (Tm) were obtained for all thirteen, and enthalpies of fusion (ΔHf) were obtained for nine congeners. Melting points of other PCNs, except for five, were found in literature. In addition, experimental ΔHf values determined by DSC were found only for 1- and 2-mono-chloronaphthalenes in the literature. The missing or uncertain values of the eight melting points and 64 enthalpies of fusion were estimated by multiple linear regressions using a set of thirteen molecular descriptors as candidates for independent variables. The stepwise model of …

Entropy of fusionPartition coefficientDifferential scanning calorimetryChemistryMolecular descriptorEnthalpy of fusionLinear regressionMelting pointThermodynamicsPhysical and Theoretical ChemistryCondensed Matter PhysicsThermal analysisInstrumentationThermochimica Acta
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Polystyrene nanoparticles in the presence of (ethylene oxide)13(propylene oxide)30(ethylene oxide)13, N,N-dimethyloctylamine-N-oxide and their mixtur…

2008

Polystyrene nanoparticles were synthesized by emulsion polymerization of styrene. They were functionalized using the conventional surfactant N,N-dimethyloctylamine-N-oxide (ODAO), the tri-block copolymer (ethylene oxide)13(propylene oxide)30(ethylene oxide)13 (L64) and their mixtures. To this purpose, dynamic light scattering and calorimetric experiments were carried out and provided information consistent to each other. The L64 adsorption is Langmuir-type in the copolymer dilute regime and generates complex structures at larger concentrations. In the region where ODAO is in the unimeric state, the adsorption process is cooperative leading to hemi-micelle formation at the polystyrene nanopa…

Ethylene OxideMaterials scienceLightSurface PropertiesOxideGeneral Physics and AstronomyEmulsion polymerizationCalorimetryTRIBLOCK COPOLYMERSStyrenechemistry.chemical_compoundDynamic light scatteringAQUEOUS-SOLUTIONSPolymer chemistryCopolymerScattering RadiationPropylene oxideSURFACTANTSPhysical and Theoretical ChemistryStyreneEthylene oxideLAPONITE CLAYWaterOxidesOctanesHEAT-CAPACITIESSolutionsBLOCK-COPOLYMERSLATEXchemistryChemical engineeringNanoparticlesPolystyrenesMASS-ACTION MODELTHERMODYNAMIC PROPERTIESAdsorptionPolystyrenePhys. Chem. Chem. Phys.
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Quantitative description of temperature induced self-aggregation thermograms determined by differential scanning calorimetry

2012

A novel thermodynamic approach for the description of differential scanning calorimetry (DSC) experiments on self-aggregating systems is derived and presented. The method is based on a mass action model where temperature dependence of aggregation numbers is considered. The validity of the model was confirmed by describing the aggregation behavior of poly(ethylene oxide)-poly(propylene oxide) block copolymers, which are well-known to exhibit a strong temperature dependence. The quantitative description of the thermograms could be performed without any discrepancy between calorimetric and van 't Hoff enthalpies, and moreover, the aggregation numbers obtained from the best fit of the DSC exper…

Ethylene oxideSelf aggregationThermodynamicsSurfaces and InterfacesCondensed Matter PhysicsTemperature inducedLight scatteringchemistry.chemical_compoundDifferential scanning calorimetrychemistryDSC Micelle copolymer calorimetryElectrochemistryCopolymerPhysical chemistryGeneral Materials SciencePropylene oxideAction modelSpectroscopySettore CHIM/02 - Chimica Fisica
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Competition between α and γ phases in isotactic polypropylene: effects of ethylene content and nucleating agents at different cooling rates

2001

Abstract The influence of ethylene content, nucleating agents and cooling rate upon the formation of γ phase in isotactic polypropylene is investigated. Detailed analysis of wide angle X-ray diffraction shows that some γ phase can appear even in copolymers of very low ethylene content (0.5 mol.%). Differential scanning calorimetry shows a double melting peak. Nucleating agents of different types are found to enhance γ phase crystallization, even in high molecular weight homopolymers. In any of the materials studied the amount of γ phase decreases with increasing cooling rate, going to zero at a cooling rate of about 10°C s−1. We interpret the observations in terms of the kinetics of growth …

EthyleneMaterials sciencePolymers and PlasticsComonomerOrganic ChemistryKineticsNucleationlaw.inventionchemistry.chemical_compoundDifferential scanning calorimetrychemistryChemical engineeringlawTacticityPolymer chemistryMaterials ChemistryCopolymerCrystallizationPolymer
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The role of crystalline, mobile amorphous and rigid amorphous fractions in the performance of recycled poly (ethylene terephthalate) (PET)

2012

[EN] The action of thermo-mechanical degradation induced by mechanical recycling of poly(ethylene terephthalate) was simulated by successive injection moulding cycles. Degradation reactions provoked chain scissions and a reduction in molar mass mainly driven by the reduction of diethyleneglycol to ethylene glycol units in the flexible domain of the PET backbone, and the formation of -OH terminated species with shorter chain length. The consequent microstructural changes were quantified taking into account a three-fraction model involving crystalline, mobile amorphous (MAF) and rigid amorphous fractions (RAF). A remarkable increase of RAF, to a detriment of MAF was observed, while the percen…

EthyleneSolucions polimèriquesPolymers and PlasticsInjection mouldingDifferential scanning calorimetry (DSC)Crystalline fractionsMechanical propertiesThermo-mechanical degradationchemistry.chemical_compoundDegradationAmorphous materialsPolymer blendsMaterials ChemistryMechanical recyclingRecyclingComposite materialDiethyleneglycolPoly(ethylene terephthalate) (PET)Injection moldingMolar massMechanical featureRecycled poly(ethylene terephthalate)Microstructural changesCondensed Matter PhysicsChain scissionRigid-amorphous fractionMechanics of MaterialsMAQUINAS Y MOTORES TERMICOSPolymer blendMaterials scienceMechanical performanceViscoelasticityEthyleneDifferential scanning calorimetrySegmental dynamicsInfrared analysis (FT-IR)Degradation reactionDifferential scanning calorimetryInjection mouldingPolyethylene terephthalatesEthylene glycolTermoplàsticsCrystalline materialsShorter chainsAmorphous solidchemistryGlass-rubber relaxationProcessing cyclesEthylene glycol
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Influence of three types of superplasticizers on tricalciumaluminate hydration in presence of gypsum.

2006

International audience; Different types of superplasticizers have been widely used over the past few decades in order to produce a more fluid or very high strength and durable concrete. These chemical admixtures interfere with the various physico-chemical processes occurring in early cement paste. In this paper we present results from a study on the influence of superplasticizers on pure tricalciumaluminate hydration in presence of gypsum. The suspensions hydration has been investigated by conductimetry, isothermal calorimetry and total organic carbon analysis of the liquid phase. The time taken for ettringite formation has been determined without superplasticizer and in presence of three d…

Ettringite[CHIM.MATE] Chemical Sciences/Material chemistryGypsumtricalcium aluminateSuperplasticizerIsothermal titration calorimetrytricalcium aluminate.[CHIM.MATE]Chemical Sciences/Material chemistryengineering.materialCement pastechemistry.chemical_compoundsuperplasticizerAdsorptionchemistryChemical engineering[ CHIM.MATE ] Chemical Sciences/Material chemistryengineeringTricalcium aluminateDissolutionhydration
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Applications of conduction calorimetry to the setting reaction of zinc phosphate dental cement

1999

The kinetics of the exothermic setting reaction of zinc phosphate dental cement can be successfully investigated by conduction calorimetry. The primary objective of this study is to examine the effects arising from the addition of various additives to the liquid and calcination of cement powder. The rate of heat evolution versus time shows the occurrence of merely one maximum. In the case of unmodified orthophosphoric acid a sharp peak occurs early after onset of mixing due to the formation of crystalline α-hopeite. Commercial cement liquids contain aluminum and zinc. From the calorimetric curves it has been found that these cations act as a setting retarders, and ensure sufficient working …

Exothermic reactionCementMaterials scienceMineralogyZinc phosphateCalorimetryCondensed Matter PhysicsChemical reactionlaw.inventionchemistry.chemical_compoundchemistryChemical engineeringlawDental cementCalcinationPhysical and Theoretical ChemistryInstrumentationZinc Phosphate CementThermochimica Acta
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Determination of Kinetic and Thermochemical Parameters of a Substitution Reaction at a Square-Planar Palladium(II) Complex in Water/AOT/n-Heptane Mic…

1995

Abstract The substitution reaction [Pd(bipy)(en)] 2+ + en → [Pd(en) 2 ] 2+ + bipy (where bipy = 2,2′-bipyridine and en = ethylenediamine) has been studied in water and water/AOT/ n -heptane microemulsions at various values of the molar ratio R ( R = [water]/[AOT]) by flow microcalorimetry. From calorimetric data, molar enthalpies of reaction and rate constants were obtained. These quantities indicate that, by increasing R , the reaction becomes less exothermic and its rate constant decreases, trending to the value observed in water. These features can be reasonably rationalized in terms of the peculiar solvation state of reactants inside the AOT reversed micelles and/or the peculiar physico…

Exothermic reactionIsothermal microcalorimetryHeptaneChemistryEnthalpySolvationEthylenediamineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryReaction rate constantOrganic chemistryPhysical chemistryMicroemulsionJournal of Colloid and Interface Science
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