Search results for "kinetics"

showing 10 items of 2224 documents

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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Relationships between kinetic constants and the amino acid composition of enzymes from the yeast Saccharomyces cerevisiae glycolysis pathway

2012

The kinetic models of metabolic pathways represent a system of biochemical reactions in terms of metabolic fluxes and enzyme kinetics. Therefore, the apparent differences of metabolic fluxes might reflect distinctive kinetic characteristics, as well as sequence-dependent properties of the employed enzymes. This study aims to examine possible linkages between kinetic constants and the amino acid (AA) composition (AAC) for enzymes from the yeast Saccharomyces cerevisiae glycolytic pathway. The values of Michaelis-Menten constant (K M), turnover number (k cat), and specificity constant (k sp = k cat/K M) were taken from BRENDA (15, 17, and 16 values, respectively) and protein sequences of nine…

chemistry.chemical_classificationSpecificity constantbiologyResearchSaccharomyces cerevisiaeMichaelis-Menten constantTurnover numberbiology.organism_classificationMichaelis–Menten kineticsGeneral Biochemistry Genetics and Molecular BiologyYeastComputer Science ApplicationsAmino acidSequence-dependent propertiesComputational MathematicsMetabolic pathwayEnzymechemistryBiochemistryGlycolytic enzymesMultivariate relationshipsEnzyme kineticsSpecificity constantEURASIP Journal on Bioinformatics and Systems Biology
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Multiple interactions between molecular and supramolecular ordering

1999

We report studies of the interplay among processes of molecular conformational changes, spinodal demixing of the solution, and molecular crosslinking involved in the physical gelation of a biopolysaccharide-water system. Multiple interactions and kinetic competition among these processes were studied under largely different absolute and relative values of their individual rates by appropriate choices of the quenching temperature at constant polymer concentration. Quenching temperature strongly affects the rate of growth but not the final value of the fractal dimension of the gel. Kinetic competition plays a central role in determining the final conformation of individual molecules and the s…

chemistry.chemical_classificationSpinodalQuenching (fluorescence)chemistryChemical physicsKineticsCondensationSupramolecular chemistryMoleculePhysical chemistryPolymerFractal dimensionPhysical Review E
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Effect of ionic liquid organizing ability and amine structure on the rate and mechanism of base induced elimination of 1,1,1-tribromo-2,2-bis(phenyl-…

2006

Abstract The kinetics of the elimination reaction of 1,1,1-tribromo-2,2-bis(phenyl-substituted)ethanes into the corresponding 1,1-dibromo-2,2-bis(phenyl-substituted)ethenes induced by amines were studied in three room temperature ionic liquids ([BMIM][BF 4 ], [BMIM][PF 6 ], [BdMIM][BF 4 ]). In order to have information about reagent–ionic liquid interactions, the reaction was carried out over the temperature range (293.1–313.1 K). To study the effect of the amine on the rate and occurrence of the elimination reaction, several primary, secondary and tertiary amines with different structure (cyclic and acyclic), basicity and steric requirements were used. The data collected show that the reac…

chemistry.chemical_classificationSteric effectsBase (chemistry)Organic ChemistryInorganic chemistryKineticsAtmospheric temperature rangeionic liquids elimination reaction base catalysisBiochemistryMedicinal chemistrychemistry.chemical_compoundElimination reactionchemistryDrug DiscoveryIonic liquidAmine gas treatingTetrahedron
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Kinetically Controlled Sequential Growth of Surface-Grafted Chiral Supramolecular Copolymers.

2016

We report a facile strategy to grow supramolecular copolymers on Au surfaces by successively exposing a surface-anchored monomer to solutions of oppositely charged peptide comonomers. Charge regulation on the active chain end of the polymer sufficiently slows down the kinetics of the self-assembly process to produce kinetically trapped copolymers at near-neutral pH. We thereby achieve architectural control at three levels: The β-sheet sequences direct the polymerization away from the surface, the height of the supramolecular copolymer brushes is well-controlled by the stepwise nature of the alternating copolymer growth, and 2D spatial resolution is realized by using micropatterned initiatin…

chemistry.chemical_classificationSurface (mathematics)Materials science010405 organic chemistryKineticsSupramolecular chemistryNanotechnologyGeneral ChemistryPolymer010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymerizationCopolymerSelf-assemblyAngewandte Chemie (International ed. in English)
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The effect of silica nanoparticles on the morphology, mechanical properties and thermal degradation kinetics of PMMA

2012

Abstract Silica–PMMA nanocomposites with different silica quantities were prepared by a melt compounding method. The effect of silica amount, in the range 1–5 wt.%, on the morphology, mechanical properties and thermal degradation kinetics of PMMA was investigated by means of transmission electron microscopy (TEM), X-ray diffractometry (XRD), dynamic mechanical analysis (DMA), thermogravimetric analyses (TGA), Fourier-transform infrared spectroscopy (FTIR), 13 C cross-polarization magic-angle spinning nuclear magnetic resonance spectroscopy ( 13 C{ 1 H} CP-MAS NMR) and measures of proton spin-lattice relaxation time in the rotating frame ( T 1 ρ ( H )), in the laboratory frame ( T 1 ( H )) a…

chemistry.chemical_classificationThermogravimetric analysisNanocompositeMaterials sciencePolymers and PlasticsPMMA Silica 13C{1H} CP-MAS NMR Degradation kineticsInfrared spectroscopyNuclear magnetic resonance spectroscopyDynamic mechanical analysisPolymerCondensed Matter PhysicsAmorphous solidChemical engineeringchemistryMechanics of MaterialsMaterials ChemistryFourier transform infrared spectroscopyComposite materialSettore CHIM/02 - Chimica Fisica
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CeO2−x nanorods with intrinsic urease-like activity

2018

The large-scale production and ecotoxicity of urea make its removal from wastewater a health and environmental challenge. Whereas the industrial removal of urea relies on hydrolysis at elevated temperatures and high pressure, nature solves the urea disposal problem with the enzyme urease under ambient conditions. We show that CeO2−x nanorods (NRs) act as the first and efficient green urease mimic that catalyzes the hydrolysis of urea under ambient conditions with an activity (kcat = 9.58 × 101 s−1) about one order of magnitude lower than that of the native jack bean urease. The surface properties of CeO2−x NRs were probed by varying the Ce4+/Ce3+ ratio through La doping. Although La substit…

chemistry.chemical_classificationUreasebiologyChemistrySynthetic membrane02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysisHydrolysischemistry.chemical_compoundEnzymeWastewaterbiology.proteinUreaGeneral Materials ScienceEnzyme kinetics0210 nano-technologyNuclear chemistryNanoscale
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Membrane-Perturbing Activities of KL4-Related Surfactant Peptides

2013

KL4 is a 21-residue peptide proposed as a potential substitute of pulmonary surfactant protein SP-B in synthetic surfactants, intended for the treatment of respiratory pathologies. The peptide, composed by leucines interrupted by lysine every four residues, was synthesized to simulate C-terminal amphipathic helical segments of SP-B. Once incorporated into lipid-protein complexes, KL4 promotes formation of interfacial films that produce and maintain surface tensions below 5 mN/m during compression-expansion cycling. Although KL4 was designed as an amphipathic helix at the membrane surface, the data on orientation and interactions of the peptide in membranes are contradictory. In the present …

chemistry.chemical_classificationVesicleKineticsBiophysicsMembrane structurePeptideCrystallographychemistry.chemical_compoundMembranePulmonary surfactantchemistryAmphiphileBiophysicsPOPCBiophysical Journal
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Time-monitoring sensor based on oxygen diffusion in an indicator/polymer matrix

2013

Abstract A time-monitoring sensor based on the oxidation of leuco methylene blue (LMB) to methylene blue (MB) was developed. The sensor changes its color from yellow to green in the presence of oxygen and was integrated into a poly(vinyl alcohol) matrix. The diffusion of the oxygen in the polymer matrix as well as the oxygen uptake due to the oxidation reaction determines the time monitoring of the sensor. A physical model has been developed that accounts for both the diffusion as well as the oxidation reaction. For this purpose, the reaction kinetics was determined experimentally. Moreover, the diffusion coefficient of oxygen was determined and concentration profiles in the polymer matrix …

chemistry.chemical_classificationVinyl alcoholChemistryDiffusionMetals and AlloysAnalytical chemistrychemistry.chemical_elementPolymerCondensed Matter PhysicsOxygenRedoxSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMatrix (chemical analysis)Chemical kineticschemistry.chemical_compoundMaterials ChemistryElectrical and Electronic EngineeringInstrumentationMethylene blueSensors and Actuators B: Chemical
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Kinetics in a Double Antibody Radioimmunoassay (RIA): Diffussion Control

2012

Competitive protein binding radioimmunoassay (CPB-RIA) is a principal method for quantifying serum C Peptide concentration. The accuracy of this method is critically dependent on factors that influence the reaction between anti-C Peptide antibody (P) with 125I-C Peptide (M). We studied the influence of initial concentration of M, ionic strength, and viscosity on the reaction between M and P. A kinetic model for the the reaction between. Such model adjusts satisfac- torily to the results. Bi-exponential and irreversible kinetics is determined. The results of the viscosity analysis show clear negative influence on the direct reaction rate. The ionic strength shows scarce influence on equilibr…

chemistry.chemical_classificationViscosityReaction rate constantChromatographychemistryIonic strengthAutomotive EngineeringKineticsAnalytical chemistryPeptideRadioimmunoassayDielectricEndothermic processAmerican Journal of Chemistry
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