Search results for "Rate constant"

showing 10 items of 224 documents

Hydration and dehydration kinetics of xylazine hydrochloride

2009

From the experiments where mixture of xylazine hydrochloride hydrate H and anhydrous X were held at constant conditions, the stable form of xylazine hydrochloride can be found out. To determine equilibrium relative humidity, the unstable form of xylazine hydrochloride was inserted in thermostated humidity chamber and its weight was recorded by weighing the sample outside the chamber. The kinetic model and the rate constant for each condition were determined. The rate constants give information regarding the speed of the process at every experimentally used relative humidity. Thus using the data in coordinates k – p for each temperature it is possible to determine the water vapor pressure of…

XylazineStereochemistryChemistry PharmaceuticalVapour pressure of waterEnthalpyAnalytical chemistryPharmaceutical ScienceXylazineReaction rate constantDrug StabilitymedicineRelative humidityDesiccationChemistryTemperaturefood and beveragesHumidityHumidityGeneral MedicinehumanitiesKineticsAnhydrousThermodynamicsCrystallizationHydrateAdrenergic alpha-Agonistsmedicine.drugPharmaceutical Development and Technology
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Rapid odorant release in mammalian odour binding proteins facilitates their temporal coupling to odorant signals.

2010

 ; We have measured the effect of rat odorant-binding protein 1 on the rates of ligand uptake and liquid-to-air transfer rates with a set of defined odorous compounds. Comparison of observed rate constants (k(obs)) with data simulated over a wide range of different kinetic and thermodynamic regimes shows that the data do not agree with the previously held view of a slow off-rate regime (k(off) <0.0004 s(-1)). We propose that a rapid koff would be a necessary requirement for such a system, since slow odorant-release rates would result in significant decorrelation between the olfactory world and odour perception. (c) 2010 Elsevier Ltd. All rights reserved.

[SDV.BIO]Life Sciences [q-bio]/BiotechnologyKineticsAnalytical chemistryOlfactionAcetatesCalorimetryIn Vitro Techniques[ SDV.BA ] Life Sciences [q-bio]/Animal biologyLigandsReceptors OdorantDNA-binding proteinMass Spectrometry03 medical and health sciences0302 clinical medicineReaction rate constantStructural BiologyODORANT-BINDING PROTEINSAnimals[INFO.INFO-BT]Computer Science [cs]/BiotechnologyMolecular Biology030304 developmental biology0303 health sciencesChemistryTemporal couplingLigand[SDV.BA]Life Sciences [q-bio]/Animal biology[ SDV.BIO ] Life Sciences [q-bio]/BiotechnologyRecombinant ProteinsRatsSmellKineticsOdorantsBiophysicsOLFACTIONThermodynamics[ INFO.INFO-BT ] Computer Science [cs]/Biotechnology030217 neurology & neurosurgerypsychological phenomena and processesSignal TransductionJournal of molecular biology
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Photocatalytic oxidation of acetonitrile in gas–solid and liquid–solid regimes

2005

Il programma NON mi ha consentito di scaricare il PDF di questo articolo. Se lo volete ditemi come inviarlo ABSTRACT Photocatalytic degradation of acetonitrile was carried out in both gas–solid and liquid–solid regimes using two commercial TiO2 catalysts (Merck and Degussa P25). For the gas–solid regime, a continuous annular photoreactor was used. The influence on photodegradation kinetics of the gas flow rate and concentrations of acetonitrile, oxygen, and water was investigated. Acetonitrile degradation products detected in the gas phase included carbon dioxide and hydrogen cyanide. The same photoactivity was exhibited in the presence and in the absence of water vapour. The liquid–solid reg…

acetonitrile degradation; heterogeneous photocatalysis; TiO2; IR investigationCyanideInorganic chemistryHeterogeneous catalysisCatalysisheterogeneous photocatalysisCatalysischemistry.chemical_compoundAdsorptionReaction rate constantchemistryair purificationPhotocatalysisacetonitrile degradationTiO2Volatile organic compoundsPhotocatalysisPhysical and Theoretical ChemistryAcetonitrilePhotodegradationIR investigationJournal of Catalysis
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Thermal Degradation of Green Asparagus Texture

2019

A cutting cell was developed to evaluate the texture of green asparagus by measuring its resistance to being cut with a wire. The cell was used in conjunction with a universal texturometer and improved on the single-point method of the Wilder fibrometer. Experimental conditions were determined for using the cell to measure the cutting resistance of asparagus subjected to different extents of heat treatment. Better discrimination between samples was obtained than with a Kramer cell. The fresh asparagus spears. were heated at temperatures between 70 and 100°C for different lengths of time and the kinetics of the degradation of texture was studied. A biphasic (two-component) behavior was obser…

biologyChemistryShear forceKineticsAnalytical chemistryMineralogyActivation energybiology.organism_classificationKinetic energyMicrobiologyReaction rate constantAsparagusTexture (crystalline)SofteningFood ScienceJournal of Food Protection
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Modeling for the active site nitrate reductase. Oxidation of the complex [MovO(O2CC(S) CH3Ph)2]− by nitrate and nitrite in methanol

1998

Abstract Under acid conditions the [MoVIO2(O2CC(S)CH1Ph)2]2 reacts with thiols to yield the monomeric [MoVO(O2CC(S)CH3Ph)2] and disulfide. The reduced complex [MoVO(O2CC(S)CH3Ph)2]− can react with NO3− and NO2− in a one-electron step yeilding respectively NO2 and NO and the original molybdenum (VI)-dioxo complex. The experimental pseudo-first-order rate constant with respect to the Mo(V) complex at 25°C was found to be kobs=2.3×10−4s−1 for NO3− and kobs=1.0×10−2 for NO2−. Oxo transfers to and from the substrate have been coupled to produce a catalytic system which turns over the reaction RSH+(No3− or NO2−)+H+a 1 2 [ RS ] 2 +( NO ] 2 or NO )+ H 2 O , in which thiols, NO1− and NO2− serve as a…

biologyInorganic chemistrySubstrate (chemistry)chemistry.chemical_elementActive siteNitrate reductaseMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundReaction rate constantchemistryMolybdenumMaterials Chemistrybiology.proteinMethanolPhysical and Theoretical ChemistryNitriteInorganica Chimica Acta
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Photokinetic examination of (Z,E,E)-4,4′-distyrylazobenzene

1995

Abstract 4,4′-Distyrylazobenzenes demonstrate a photokinetic equilibrium and a superimposed thermal backward reaction in which the absorption coefficient of one of the partners in the equilibrium is principally unknown. Using the dependence of the photostationary state on the irradiation intensity, the photochemical quantum yields ϕ 1 A and ϕ 2 B were determined, as well as the thermal rate constant k , as a function of the irradiation and observation wavelengths. Experimental difficulties and the wavelength dependence of ϕ 1 A and ϕ 2 B are discussed.

business.industryChemistryGeneral Chemical EngineeringGeneral Physics and AstronomyQuantum yieldGeneral ChemistryMolecular electronic transitionWavelengthOpticsReaction rate constantPhotostationary stateAttenuation coefficientAbsorptanceIrradiationAtomic physicsbusinessJournal of Photochemistry and Photobiology A: Chemistry
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Synthesis of pentafluorophenyl(meth)acrylate polymers: New precursor polymers for the synthesis of multifunctional materials

2005

Pentafluorophenyl acrylate and -methacrylate were polymerized using AIBN as a thermal initiator. The obtained polymers were soluble polymeric active esters that could be used for the preparation of multifunctional polymers. The reactivity of poly(pentafluorophenylacrylate) and poly(pentafluorophenylmethacrylate) towards primary and secondary amines, as well as alcohols was investigated in a quantitative way. Both poly(active esters) reacted satisfactorily with aliphatic primary and secondary amines but only low conversion was found in the case of aromatic amines. Conversions of only 30% were reached when poly(pentafluorophenylacrylate) was treated with one equivalent of alcohol under base c…

chemistry.chemical_classificationAcrylatePolymers and PlasticsChemistryOrganic ChemistryGeneral Physics and AstronomyAlcoholPolymerMethacrylateCatalysischemistry.chemical_compoundReaction rate constantPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryReactivity (chemistry)European Polymer Journal
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Kinetic Investigation on Metal Free Anionic Polymerization of Methyl Methacrylate Using Tetraphenylphosphonium as the Counterion in Tetrahydrofuran

1997

The anionic polymerization of methyl methacrylate using tetraphenylphosphonium triphenylmethanide as an initiator proceeds in a living manner even at room temperature. The rate constants of propagation were measured between -20 and +20 °C using a flow tube reactor. At 0 °C the reaction half-lives range from 0.3 to 1 s. The polymerization follows first-order kinetics with respect to monomer conversion (with a short induction period) and shows a linear dependence of the number-average degree of polymerization on conversion with high initiator efficiencies and narrow molecular weight distributions (M w /M n < 1.1). The dependence of the measured rate constants on the active center concentratio…

chemistry.chemical_classificationArrhenius equationPolymers and PlasticsOrganic ChemistrySolution polymerizationDegree of polymerizationInorganic Chemistrychemistry.chemical_compoundsymbols.namesakeAnionic addition polymerizationReaction rate constantchemistryPolymerizationPolymer chemistryMaterials ChemistrysymbolsPhysical chemistryCounterionMethyl methacrylateMacromolecules
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Proteolytic cleavage of soybean Bowman-Birk inhibitor monitored by means of high-performance capillary electrophoresis. Implications for the mechanis…

1996

The hydrolysis of the soybean Bowman-Birk inhibitor in the presence of catalytic amounts of bovine trypsin and the formation of the non-covalent enzyme-inhibitor complex with an equimolar amount of enzyme are monitored by means of high-performance capillary electrophoresis (HPCE). The inhibitor is cleaved in the trypsin-reactive and more slowly in the chymotrypsin-reactive subdomain. HPCE proves itself as the only reliable analytical tool to monitor these reactions in clear contrast to classical electrophoretic, chromatographic and enzymatic methods. The most efficient separation of the intact and the two active site cleaved forms of the inhibitor was achieved in borate buffer at pH 10.0. T…

chemistry.chemical_classificationBinding SitesChromatographybiologyChemistryHydrolysisMolecular Sequence DataBiophysicsElectrophoresis CapillaryActive siteCleavage (embryo)BiochemistryCatalysisProtein Structure TertiaryKineticsElectrophoresisHydrolysisReaction rate constantEnzymeCapillary electrophoresisBiochemistryEnzyme inhibitorbiology.proteinAmino Acid SequenceTrypsin Inhibitor Bowman-Birk SoybeanJournal of Biochemical and Biophysical Methods
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On the behaviour of the (Z)-Phenylhydrazones of some 5-alkyl-3-benzoyl-1,2,4-oxadiazoles in solution and in the gas phase: kinetic and spectrometric …

2008

Abstract Rate constants, k A,R , for the rearrangement of the ( Z )-phenylhydrazones ( 1a – e ) of a series of 5-alkyl-3-benzoyl-1,2,4-oxadiazoles substituted at C(5) with linear alkyl chains of different length (from C 4 up to C 12 ) into the relevant 4-acylamino-2,5-diphenyl-1,2,3-triazoles ( 2a – e ) have been measured in dioxan/water in the base-catalyzed region (pS + 10.5–12.6). For each substrate log  k A,R are linearly related to pS + . The significant decrease of the slopes of these straight lines (from 0.96 down to 0.78) upon increasing the length of the linear alkyl chain at C(5) and that of the reactivity (down to 14–26%) upon increasing the substrate concentration suggest a decr…

chemistry.chemical_classificationDirect evidenceStereochemistryOrganic ChemistrySubstrate (chemistry)124-oxadiazoleKinetic energyBiochemistryCrystallographyReaction rate constantchemistryDrug DiscoveryProton NMRReactivity (chemistry)Self-assemblymononuclear rearrangementAlkyl
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