Search results for "dynamics."

showing 10 items of 9637 documents

Molecular modeling studies of interactions between styrene–butadiene latex and sodium polyacrylate polymer surface

2010

Abstract The interaction between two important paper coating ingredients, sodium polyacrylate polymer dispersing agent and styrene–butadiene latex binder, was studied using classical force field and quantum chemical methods. The objective was to understand the adsorption of styrene–butadiene latex on the sodium polyacrylate polymer model surfaces at 300 K using molecular dynamics simulations. A quantum mechanical ab initio Hartree–Fock method was also used to obtain detailed information about the above interactions. In addition, the effect of moisture was investigated. Calculations showed that the conformation and orientation of styrene–butadiene latex, the number of carboxylate groups in t…

chemistry.chemical_classificationStyrene-butadieneSodium polyacrylateSodiumchemistry.chemical_elementPolymerCondensed Matter PhysicsBiochemistryDispersantchemistry.chemical_compoundMolecular dynamicsAdsorptionchemistryPolymer chemistryMoleculePhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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Impact of surface state on polyethylene glycol conformation confined inside a nanopore.

2021

Solid-state nanopores are a promising platform for characterizing proteins. In order to improve their lifetime and prevent fouling, Polyethylene Glycol (PEG) grafting is one of the most efficient and low-cost solutions. Different models to calculate the PEG thickness do not consider their interaction with the nanopore inner surface nor the effect of confinement. Here, we investigate by molecular dynamic simulation the PEG conformation inside a nanopore in the case of hydrophobic and hydrophilic nanopores. Our results reveal that the nanopore inner surface plays a role in the PEG organization and, thus, in the speed of the salt constituent. The resulting pair interaction between PEG and its …

chemistry.chemical_classificationSurface (mathematics)Materials science010304 chemical physicsFoulingtechnology industry and agricultureGeneral Physics and AstronomySalt (chemistry)Polyethylene glycol010402 general chemistryGrafting01 natural sciences0104 chemical sciencesMolecular dynamicsNanoporechemistry.chemical_compoundChemical engineeringchemistry0103 physical sciencesPEG ratioPhysical and Theoretical ChemistryThe Journal of chemical physics
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Networks of Partially Hydrogenatedcis-1,4-Polybutadiene and ‘Rigid Rods’

1996

Networks of 'flexible' and 'rigid' chains were synthesized. As 'flexible' component we have used different partially hydrogenated cis-1,4-polybutadiene. The 'rigid' component was synthesized from bis(1,2,4-triazoline-3,5-dione)s and biscyclohexadienes via repetitive Diels-Alder reaction. A slight excess of bis(1,2, 4-triazoline-3,5-dione)s leads to polymers with 1,2,4-triazoline-3,5-dione end groups, which can easily react with the partially hydrogenated cis-1,4-polybutadiene. The influence of the extent of hydrogenation and the amount of crosslinker on the mechanical and thermal behaviour is described.

chemistry.chemical_classificationTelechelic polymerMaterials sciencePolymers and PlasticsComponent (thermodynamics)Organic ChemistryPolymerRodPolybutadienechemistryPolymer chemistryMaterials ChemistryEne reactionPolyimidePolymer International
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Forever Young: Structural Stability of Telomeric Guanine-Quadruplexes in Presence of Oxidative DNA Lesions

2020

AbstractHuman telomeric DNA (h-Telo), in G-quadruplex (G4) conformation, is characterized by a remarkable structural stability that confers it the capacity to resist to oxidative stress producing one or even clustered 8-oxoguanine lesions. We present a combined experimental/computational investigation, by using circular dichroism in aqueous solutions, cellular immunofluorescence assays and molecular dynamics (MD) simulations, that identifies the crucial role of the stability of G4s to oxidative lesions, related also to their biological role as inhibitors of telomerase, an enzyme overexpressed in most cancers associated to oxidative stress.

chemistry.chemical_classificationTelomeraseCircular dichroismmedicine.diagnostic_testOxidative phosphorylationImmunofluorescencemedicine.disease_causeMolecular dynamicschemistry.chemical_compoundEnzymechemistrymedicineBiophysicsDNAOxidative stress
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On The Incompatibility of Dextran and Pullulan in Aqueous Solutions and Its Modeling

2012

Joint aqueous solutions of branched dextran and linear pullulan are investigated with respect to their phase separation. The experiments demonstrate that the polymers are – depending on the molar mass of dextran – incompatible in aqueous solutions despite their chemical similarity. This finding can be modeled on the basis of an approach accounting for chain connectivity and conformational relaxation of the components. According to these calculations, the polymers exhibit a miscibility gap in joint solutions despite the favorable interactions between them. Using information on the subsystems H2O/dextran and H2O/pullulan, the assumption of complete miscibility of the polysaccharides is requir…

chemistry.chemical_classificationTernary numeral systemAqueous solutionMolar massPolymers and PlasticsChemistrySpinodal decompositionOrganic ChemistryThermodynamicsPullulanPolymerCondensed Matter PhysicsMiscibilitychemistry.chemical_compoundDextranPolymer chemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Heat capacities of butanol and pentanol in aqueous dodecyltrimethylammonium bromide solutions

1987

Heat capacities of the ternary systems water-dodecyltrimethylammonium bromide (DTAB)-butanol and water-DTAB-pentanol were measured at 25°C. The standard partial molar heat capacities of pentanol in micellar solutions show a maximum at about 0.35 mol-kg−1 DTAB that has been attributed to a micellar structural transition. This maximum tends to vanish by increasing the alcohol concentration and by decreasing the alcohol alkyl chain length; in the case of butanol it was not detected. The behavior of the standard partial molar heat capacities of alcohols in micellar solutions in the region above the cmc and below the structural transition was explained using a previously reported mass-action mod…

chemistry.chemical_classificationTernary numeral systemChemistryButanolInorganic chemistryDistribution constantBiophysicsThermodynamicsAlcoholBiochemistryMicelleHeat capacitychemistry.chemical_compoundMicellar solutionslipids (amino acids peptides and proteins)Physical and Theoretical ChemistryMolecular BiologyAlkylJournal of Solution Chemistry
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Viscometric behaviour of polymer blends based on poly (vinylidene fluoride)

1994

The viscosity behaviour of dilute dimethylformamide solutions of poly(vinylidene fluoride)-poly (methyl methacrylate) and poly(vinylidene fluoride)-polystyrene has been studied at 25°C. The polymer concentration ranges are such that neither phase separation nor microgel formation occurs, although we are very close to theta conditions. The intrinsic viscosity and viscosity interaction parameter of the ternary mixtures have been calculated. The estimation of the compatibility of the above polymer pairs has been studied based on: a) specific viscosities; b) viscosity interaction parameters, according to Krigbaum and Wall formalism, and c) viscosity interaction parameters of a system formed by …

chemistry.chemical_classificationTernary numeral systemMaterials sciencePolymers and PlasticsIntrinsic viscosityRelative viscosityPolymerFlory–Huggins solution theoryPhysics::Fluid DynamicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundColloid and Surface ChemistrychemistryChemical engineeringPolymer chemistryMaterials ChemistryPolymer blendPhysics::Chemical PhysicsPhysical and Theoretical ChemistryMethyl methacrylateFluorideColloid & Polymer Science
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Ternary Polymer Solutions with Hydrogen Bonds, 1

2007

The Flory Huggins methodology coupled to AET has been extended to ternary polymer systems, in particular to solvent (A)/polymer 1 (B)/polymer 2 (C) systems, with the two polymers displaying H-bonding interactions. Because the H-bonding can perturb the randomness of polymeric conformations, the change in Gibbs free energy of mixing, AG, should arise from changes in combinatorial entropy as well as in interaction energy. The combinatorial part of AG is evaluated through AET as a function of the association constant η between B and C components, the autoassociation constant a between B components, and the independent number m of interaction sites of acceptor C. The enthalpic contribution is ev…

chemistry.chemical_classificationTernary numeral systemPolymers and PlasticsChemistryHydrogen bondOrganic ChemistryThermodynamicsInteraction energyPolymerEntropy of mixingFlory–Huggins solution theoryCondensed Matter PhysicsAcceptorInorganic ChemistryMaterials ChemistryTernary operationMacromolecular Theory and Simulations
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Correlation between transport and equilibrium properties through the ternary interaction parameter for cosolvent and cononsolvent polymeric systems

1992

A study of the ternary polymer systems dimethyl formamide-ethyl acetate-polystyrene, chloroform-1,4 dioxane-polystyrene and tetrahydrofuran-chloroform-polystyrene was carried out by viscosity and light scattering at 298 K. A good correlation has been found between the excess intrinsic viscosity, unperturbed polymer dimensions, second virial coefficient and the excess Gibbs free energy by using a ternary interaction parameter, dependent on molecular weight. This modification enables the conversion between transport and equilibrium properties.

chemistry.chemical_classificationTernary numeral systemPolymers and PlasticsChemistryIntrinsic viscosityThermodynamicsPolymerFlory–Huggins solution theoryGibbs free energyViscositysymbols.namesakeColloid and Surface ChemistryVirial coefficientMaterials ChemistrysymbolsPhysical and Theoretical ChemistryTernary operationColloid & Polymer Science
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Interfacial tension between coexisting polymer solutions in mixed solvents and its correlation with bulk thermodynamics: phase equilibria (liquid/gas…

2002

Abstract Vapor pressures, phase equilibria and interfacial tensions σ were measured for solutions of poly(dimethylsiloxane) (PDMS, M w [equals]75 kg/mol and M n [equals]50 kg/mol) in mixed solvents of toluene (TL) and ethanol (EtOH) at 30, 40, 50 and 60 °C. The experimental ternary phase diagrams can be modeled quantitatively from the determined concentration and temperature dependent binary interaction parameters χ ij if the experimentally inaccessible composition dependence of χ EtOH/PDMS is adjusted. The relations between σ and the equation of state of the system differ from that applying to single solvents. The exponents as well as the amplitude prefactors of the corresponding scaling l…

chemistry.chemical_classificationTernary numeral systemPolymers and PlasticsChemistryLiquid gasOrganic ChemistryThermodynamicsPolymerTolueneSurface tensionchemistry.chemical_compoundAmplitudeCritical point (thermodynamics)Materials ChemistryPhase diagramPolymer
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