Search results for "Kinetic"

showing 10 items of 3064 documents

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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Experimental organic matter maturation at 2kbar: Heat-up effect to low temperatures on vitrinite reflectance

2012

Abstract An experimental study was performed to evaluate the effect of heat-up to various low temperatures on vitrinite reflectance ( VR ) at 2 kbar employing the same previously used heat-up procedures, starting material and apparatus. Heat-up is the isobaric experimental procedure consisting of the increase in temperature of the laboratory vitrinite maturation from room temperature to the desired run temperature T end of heat-up at which the isobaric-isothermal maturation starts. Experiments employed cold-seal pressure vessels with classical heat-up devices and were carried out on wet (water added) xylite of swamp cypress. Confined system maturation experiments were conducted at 2 kbar an…

chemistry.chemical_classificationVitrinite reflectance020209 energyStratigraphyKinetic analysisThermodynamicsMineralogyGeology02 engineering and technologyRate equation010502 geochemistry & geophysicsKinetic energy01 natural sciencesIsothermal processFuel Technologychemistry0202 electrical engineering electronic engineering information engineeringIsobaric processEconomic GeologyOrganic matterVitrinite0105 earth and related environmental sciencesInternational Journal of Coal Geology
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The use of master curves to describe the simultaneous effect of cooling rate and pressure on polymer crystallization

2003

In a previous work a master-curve approach was applied to experimental density data to explain isotactic polypropylene (iPP) behaviour under pressure and high cooling rates. Suitable samples were prepared by solidification from the melt under various cooling rate and pressure conditions with the help of a special apparatus based on a modified injection moulding machine. The approach here reported is more general than the case study previously shown, and is suitable to be applied to several materials and for different measures related to crystalline content. The proposed simple model is able to predict successfully the final polymer properties (density, micro-hardness, crystallinity) by supe…

chemistry.chemical_classificationWork (thermodynamics)Settore ING-IND/24 - Principi Di Ingegneria ChimicaMaterials sciencePolymers and PlasticsCrystallization of polymersOrganic ChemistrySettore ING-IND/34 - Bioingegneria IndustrialePolymerCrystallization Kineticslaw.inventionCrystallinitySuperposition principlechemistrylawTacticityMaterials ChemistryInjection mouldingComposite materialCrystallization
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Aggregation of sponge cells. Isolation and characterization of an inhibitor of aggregation receptor from the cell surface.

1979

From the cell membranes of the sponge Geodia cydonium a component was isolated and purified which inhibits the aggregation factor isolated from the same source; the component was termed anti-aggregation receptor. This molecule was characterized as a glycoprotein (54% neutral carbohydrate) and its molecular weight is in the range of 180,000 One biological site of the anti-aggregation receptor was determined to be D-galactose. Indirect evidence presented seems to indicate that this molecule is present in an active form in aggregation-deficient cells and absent in aggregation-susceptible cells.

chemistry.chemical_classificationbiologyCellCell MembraneGuanosine MonophosphateMembrane ProteinsCarbohydratebiology.organism_classificationBiochemistryPoriferaMolecular WeightSpongeKineticsMembranemedicine.anatomical_structurechemistryBiochemistrymedicineMoleculeAnimalsGeodiaGlycoproteinReceptorCell AggregationEuropean journal of biochemistry
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Kinetics of alkaline phosphatase from pig kidney. Influence of complexing agents on stability and activity

1976

Metal ion-complexing agents, like KCN, EDTA etc., inactivate alkaline phosphatase of pig kidney. This inactivation is reversible at low concentrations of the complexing agents and irreversible at high concentrations. The reversible inhibition is probably due to removal of Zn2+ ions from the active site, where they are necessary for catalytic action, whereas the irreversible inhibition results from the removal of Zn2+ ions necessary for preservation of the structure. The inactivation is pseudo-first order. It depends on the concentration, size and charge of the complexing agents. β-Glycerophosphate and Mg2+ ions protect the enzyme from inactivation by complexing agents. Quantitative examinat…

chemistry.chemical_classificationbiologyDimerInorganic chemistryAllosteric regulationKineticsSubstrate (chemistry)Active siteCell BiologyCombinatorial chemistryBiochemistrychemistry.chemical_compoundEnzymechemistrybiology.proteinAlkaline phosphataseChelationMolecular BiologyBiochemical Journal
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Differential behaviour of Pseudomonas sp. 42A2 LipC, a lipase showing greater versatility than its counterpart LipA

2009

Abstract Growth of Pseudomonas sp. 42A2 on oleic acid releases polymerized hydroxy-fatty acids as a result of several enzymatic conversions that could involve one or more lipases. To test this hypothesis, the lipolytic system of strain Pseudomonas sp. 42A2 was analyzed, revealing the presence of at least an intracellular carboxylesterase and a secreted lipase. Consensus primers derived from a conserved region of bacterial lipase subfamilies I.1 and I.2 allowed isolation of two secreted lipase genes, lipA and lipC, highly homologous to those of Pseudomonas aeruginosa PAO1. Homologous cloning of the isolated lipA and lipC genes was performed in Pseudomonas sp. 42A2 for LipA and LipC over-expr…

chemistry.chemical_classificationbiologyStrain (chemistry)PseudomonasFatty acidLipaseGeneral Medicinebiology.organism_classificationBiochemistrySubstrate SpecificityIsoenzymesCarboxylesteraseOleic acidchemistry.chemical_compoundEnzymeBacterial ProteinschemistryBiochemistryPseudomonasEnzyme Stabilitybiology.proteinEnzyme kineticsLipaseBiochimie
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