Search results for "NUMBER"

showing 10 items of 3939 documents

Interfaces between coexisting phases in polymer mixtures: What can we learn from Monte Carlo simulations?

1999

Symmetric binary polymer mixtures are studied by Monte Carlo simulation of the bond fluctuation model, considering both interfaces between coexisting bulk phases and interfaces confined in thin films. It is found that the critical behavior of interfacial tension and width is compatible with that of the Ising model, as expected from the universality principle. In the strong segregation limit, only qualitative but not quantitative agreement with the self-consistent field (SCF) theory is found. It is argued that the SCF theory requires √ 6 X √D for short-range forces, in agreement with experiment.

chemistry.chemical_classificationPolymers and PlasticsCondensed matter physicsOrganic ChemistryMonte Carlo methodBinary numberPolymerCondensed Matter PhysicsUniversality (dynamical systems)Condensed Matter::Soft Condensed MatterSurface tensionchemistryMaterials ChemistryIsing modelPolymer blendStatistical physicsThin filmMacromolecular Symposia
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Simulation of first- and second-order transitions in asymmetric polymer mixtures

1993

The critical properties of dense asymmetric binary polymer mixtures are studied by grand canonical simulations within the framework of the 3-dimensional bond fluctuation lattice model. The monomers interact with each other via a potential ranging over the entire first peak of the pair distribution. An asymmetry is realized by giving the ratio of interactions λ = ∈AA/∈BB between monomers of the A-species and of the B-species a value different from 1. Using multiple histogram extrapolation techniques for the data analysis, the two phase region, which is a line of first-order transitions driven by the chemical potential difference, and the critical point are determined for a mixture of chains …

chemistry.chemical_classificationPolymers and PlasticsCondensed matter physicsmedia_common.quotation_subjectOrganic ChemistryExtrapolationThermodynamicsBinary numberPolymerCondensed Matter PhysicsAsymmetrychemistry.chemical_compoundMonomerchemistryPotential differenceCritical point (thermodynamics)HistogramMaterials Chemistrymedia_commonMakromolekulare Chemie. Macromolecular Symposia
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New Thermoshrinkable Materials of Radiation Modified Polypropylene-Elastomer Composites with Cross-Linking Agents

2014

In this work, electron beam modified heterogeneous composites of isotactic polypropylene (PP) with chlorinated polyethylene (CPE) have been investigated. The PP/CPE blend composites with an excess of elastomer (30/70 wt%) have been modified with trimethylolpropane triacrylate (TMPTA) and bisphenol-A-dimethacrylate (BPDMA) cross-linking agents and have been irradiated with accelerated electrons up to ionizing radiation doses from 25 to 150 kGy. The internal stresses characterizing the thermoshrinkage properties (TMP) thermorelaxation stresses formed in thermal heating and the residual stresses resulting in the process of full setting and cooling of materials have been investigated for radiat…

chemistry.chemical_classificationPolypropyleneMaterials scienceMechanical EngineeringComposite numberPolymerTMPTAElastomerchemistry.chemical_compoundLow-density polyethylenechemistryMechanics of MaterialsResidual stressTacticityGeneral Materials ScienceComposite materialKey Engineering Materials
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Temperature effects on counterion binding to spherical polyelectrolytes: the charge-discharge transition of lignosulfonate

1995

Abstract The effect of temperature on the effective charge numbers and diffusion coefficients of polyelectrolytes has not nobee dealth with in many studies. The present study concerns the temperature behavior of lignosulfonate. Lignosulfonate is a polydisperse polyelectrolyte whose molecules are compact spheres in aqueous solutions. One of its most remarkable properties is that is loses its charge in 0.1 M NaCl aqueous solution at about 40°C. In order to explain this charge-discharge transition, a theory for ion binding to spherical polyelectrolytes based on the relative population of two hydration states of the charged groups is presented. The water molecules adjacent to the charged groups…

chemistry.chemical_classificationQuantitative Biology::Biomoleculeseducation.field_of_studyGlobular proteinInorganic chemistryPopulationBiophysicsCharge numberElectrolyteIon-associationEffective nuclear chargePolyelectrolyteCondensed Matter::Soft Condensed MatterIon bindingchemistryChemical physicsElectrochemistryPhysical and Theoretical ChemistryeducationBioelectrochemistry and Bioenergetics
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Self-Diffusion of Small Molecules into Rubbery Polymers: A Lattice Free-Volume Theory

2010

In the framework of the Free Volume Theory, a new equation was derived for the evaluation of self-diffusion coefficients of small molecules in polymers above the mixture glass transition temperature. The derivation of the equation turned out to be straightforward once the equivalence between the free-volume and the unoccupied volume given by Thermodynamic Lattice Theories is assumed. A parameter evaluation scheme is proposed, which is substantially simpler compared to the conventional Vrentas-Duda approach, even without losing generality. The key assumption is discussed and its consistency is verified from a numerical viewpoint. A comparison with experimental solvent self-diffusion coeffici…

chemistry.chemical_classificationSelf-diffusionPolymers and PlasticsChemistrydiffusionThermodynamicsConcentration effectBinary numbermodelingPolymerCondensed Matter PhysicsSmall moleculeAmorphous solidfree-volumethermodynamicLattice (order)Materials ChemistryamorphouPhysical and Theoretical ChemistryGlass transition
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Molecular “Floppyness” and the Lewis Acidity of Silanes: A Density Functional Theory Study

2001

A comprehensive set of Lewis acid-base adducts of silanes was investigated by means of the density functional theory geometry optimization [B3LYP/6−31G(d)], and thermochemical calculations, [B3LYP/6−311+G(2d,p)//B3LYP/6−31G(d)]. Complex formation was found to weaken Si−Cl and Si−Br bonds more than Si−F or Si−H bonds. Comparable distances between Si and a Lewis base L (L = NH3, OH2, F−) are shorter in hexa- than in pentacoordinated complexes. The molecular structures of the pentacoordinated Si complexes allowed for a mapping of an SN2 reaction pathway by correlating the lengths of the Si−X and Si−L bonds. Complex formation was found to be exothermic for most of the coordination compounds, an…

chemistry.chemical_classificationSilanesStereochemistryEnthalpyIonic bondingCoordination complexAdductInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryDonor numberThermochemistryLewis acids and basesEuropean Journal of Inorganic Chemistry
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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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Mode I fracture toughness behavior of hydro-thermally aged carbon fibre reinforced DGEBA-HHPA-PES systems

2012

In this work the Mode I fracture toughness behavior of unidirectional CFRP laminates is investigated by means of Double Cantilever Beam (DCB) tests. The composite samples were manufactured by thermal curing after impregnation of a Carbon fabric with a DGEBA epoxy and anhydride HHPA curing agent. One resin batch was also mixed with a PES thermoplastic monomer to enhance the matrix toughness. Two lots of samples, toughened and un-toughened, were then left to soak in hot water to achieve various degrees of aging. The influence of matrix toughening and hydrothermal aging on the delamination behavior of the composite have then been assessed and correlated with characterization data from Dynamic …

chemistry.chemical_classificationToughnessMaterials scienceThermoplasticScanning electron microscopeComposite numberEpoxyDynamic mechanical analysisFracture toughnessSettore ING-IND/22 - Scienza E Tecnologia Dei Materialichemistryvisual_artCFRP Delamination Fracture Toughness Epoxy Resins Hydrothermal Agingvisual_art.visual_art_mediumComposite materialCuring (chemistry)
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Bio-inspired surface modification of iron oxide nanoparticles for active stabilization in hydrogels

2020

Biological materials employ a variety of dynamic interactions in sophisticated composite structures to function adaptively on different time and length scales. Inspired by such designs we develop a novel surface modification approach to promote dynamic interactions between nanoparticles and polymer chains in physical and double network hydrogels. Physical hydrogels are formed via reversible complexation of borate ions with poly(vinyl alcohol) (PVA) and chemical crosslinks are introduced by electron beam irradiation. Dopamine is used for surface modification of magnetic iron oxide nanoparticles (MNPs) in two different ways: the direct treatment results in anchoring via catechol groups, where…

chemistry.chemical_classificationVinyl alcoholMaterials scienceComposite numberNanoparticle02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesColloidchemistry.chemical_compoundchemistryChemical engineeringSelf-healing hydrogelsSurface modification0210 nano-technologyIron oxide nanoparticlesSoft Matter
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The Mechanism of Action of Carbonic Anhydrase

1990

A survey of the structure-function relationship in the enzyme carbonic anhydrase is presented. The coordination number around the metal ion in derivatives inhibited with some anions is stressed as well as the role of the cavity in determining the coordination number. Inferences on the enzyme-substrate interactions are presented.

chemistry.chemical_classificationbiologyChemistryCoordination numberCombinatorial chemistryMetalEnzymeMechanism of actionvisual_artCarbonic anhydrasemedicinevisual_art.visual_art_mediumbiology.proteinmedicine.symptom
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