Search results for " rate constant"

showing 10 items of 220 documents

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

Pressure dependence in the methyl vinyl ketone + OH and methacrolein + OH oxidation reactions: an electronic structure study.

2005

High-level electronic structure calculations were carried out for the study of the reaction pathways in the OH-initiated oxidations of methyl vinyl ketone (MVK) and methacrolein (MACR). For the two conformers of MVK (called synperiplanar and antiperiplanar), the addition channels of OH to the terminal and central carbon atom of the double bond dominate the overall rate constant, whereas the abstraction of the methyl hydrogen atoms has no significant kinetic role. In the case of MACR, only the antiperiplanar conformer is important in its reactivity. In addition, the lower Gibbs free energy barrier for MACR corresponds to the aldehydic hydrogen abstraction reaction, which will be somewhat mor…

chemistry.chemical_classificationDouble bondChemistryHydroxyl RadicalMethacroleinElectronsHydrogen atom abstractionPhotochemistryAtomic and Molecular Physics and OpticsButanonesGibbs free energysymbols.namesakechemistry.chemical_compoundReaction rate constantModels ChemicalAlkane stereochemistryMethyl vinyl ketonesymbolsPressureOrganic chemistryThermodynamicsReactivity (chemistry)Physical and Theoretical ChemistryAcroleinOxidation-ReductionChemphyschem : a European journal of chemical physics and physical chemistry
researchProduct

Environmentally relevant precursors of carbonyl sulfide in aquatic systems

1997

Seawater solutions of environmentally relevant organosulfur compounds, commercial humic acid (HA), and natural dissolved organic matter (DOM) were incubated with and without UV light in order to determine the carbonyl sulfide (COS) producing capabilities of these compounds. COS dark- and photo-production rate constants were determined for dilute solutions of the organosulfur compounds (μmol l−1) and HA/DOM (mg l−1). Dissolved COS was determined using a purge and cryogenic trap method followed by GC/FPD detection. COS was produced in considerable amounts both non-photochemically and photochemically from the reduced form of free acid of glutathione (GSH) and photochemically from cysteine (CYS…

chemistry.chemical_classificationGeneral ChemistryGlutathioneOceanographychemistry.chemical_compoundReaction rate constantchemistryDissolved organic carbonEnvironmental ChemistryOrganic chemistryHumic acidSeawaterOrganosulfur compoundsWater Science and TechnologyCysteineCarbonyl sulfideMarine Chemistry
researchProduct

A study of the enolization of some alkyl ketones in lyomesophases formed by alkylammonium surfactants

1988

The kinetics of enolization of acetone, 3-pentanone, and 6-undecanone have been studied in lyotropic systems in the isotropic, nematic, and lamellar phases. The data, analysed in terms of spontaneous and acid-catalyzed rate constants, do not show any relevant influence of the physical nature of the phase. Effects are instead observed in relation to the length of the alkyl chains of the ketones and the type of the amphiphilic molecule. 6-undecanone has a surprising effect in stabilizing ordered mesophases.

chemistry.chemical_classificationMaterials scienceKineticsGeneral ChemistryKeto–enol tautomerismCondensed Matter PhysicsCrystallographyReaction rate constantchemistryLiquid crystalPhase (matter)LyotropicOrganic chemistryGeneral Materials ScienceLamellar structureAlkylLiquid Crystals
researchProduct