Search results for " method"

showing 10 items of 10455 documents

How does the pattern of grafting points influence the structure of one-component and mixed polymer brushes?

2005

Using Monte Carlo simulations of a coarse-grained bead-spring model we study the lateral structure formation of one-component polymer brushes in a bad solvent and of a mixed polymer brush upon increasing the incompatibility of the two species. We compare the morphology of the brush with a regular distribution of grafting points and with a random arrangement. Density or composition fluctuations of the grafting points enhance the formation of irregular structures but randomness prevents the formation of long-range order. Even small fluctuations of the grafting points are sufficient to pin the lateral structures of the brush.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesStructure formationMaterials scienceMorphology (linguistics)Monte Carlo methodGeneral Physics and AstronomyBrushNanotechnologyPolymerPolymer brushGraftinglaw.inventionCondensed Matter::Soft Condensed MatterComputer Science::GraphicschemistrylawComposite materialRandomnessEurophysics Letters (EPL)
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Entropy theory and glass transition: A test by Monte Carlo simulation

1997

This article reviews the results of a test of the Gibbs-DiMarzio theory by Monte Carlo Simulation. The simulation employed the bond-fluctuation model on a simple cubic lattice. This model incorporates two kinds of interactions: the excluded volume interaction among all monomers of the melt and an internal energy of the chains, which favors large bonds and makes the chains stiffen with decreasing temperature. The stiffening of the chains leads to an increase of their volume requirements, which competes with the packing constraints at low temperatures. This competition strongly slows down the structural relaxation of the melt and induces the glassy behavior. The model therefore takes into acc…

chemistry.chemical_classificationQuantitative Biology::Biomoleculesbond-fluctuation modelMaterials scienceInternal energyMonte Carlo methodGibbs-DiMarzio theoryGeneral EngineeringThermodynamicsSimple cubic latticePolymerArticleStiffeningCondensed Matter::Soft Condensed Matterentropy measurementchemistryExcluded volumeAdam-Gibbs theoryEntropy (information theory)chemical potentialglass transitionStatistical physicsdiffusion coefficientGlass transitionMonte Carlo simulation
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Interfacial properties of glassy polymer melts: A Monte Carlo study

1996

The properties of the interface between a polymer melt and a solid wall are studied over a wide range of temperatures by dynamic Monte Carlo simulations. It is shown that in the supercooled state near the glass transition of the melt an “interphase” forms, the structure of which is influenced by the wall. The thickness of this interphase is determined from the monomer density profile near the surface and is strongly temperature dependent. At low glass-like temperatures it is larger than the bulk radius of gyration of the chains.

chemistry.chemical_classificationRange (particle radiation)Materials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerCondensed Matter PhysicsCondensed Matter::Disordered Systems and Neural NetworksCondensed Matter::Soft Condensed MatterCrystallographychemistry.chemical_compoundMonomerchemistryMaterials ChemistryRadius of gyrationInterphaseSupercoolingGlass transitionMacromolecular Symposia
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Polymer translocation through a nanopore induced by adsorption: Monte Carlo simulation of a coarse-grained model

2004

Dynamic Monte Carlo simulation of a bead-spring model of flexible macromolecules threading through a very narrow pore in a very thin rigid membrane are presented, assuming at the cis side of the membrane a purely repulsive monomer-wall interaction, while the trans side is attractive. Two choices of monomer-wall attraction epsilon are considered, one choice is slightly below and the other slightly above the "mushroom to pancake" adsorption threshold epsilon(c) for an infinitely long chain. Studying chain lengths N=32, 64, 128, and 256 and varying the number of monomers N(trans) (time t=0) that have already passed the pore when the simulation started, over a wide range, we find for epsiloneps…

chemistry.chemical_classificationRange (particle radiation)Monte Carlo methodGeneral Physics and AstronomyPolymerNanoporeAdsorptionMembranechemistryChemical physicsStatistical physicsPhysical and Theoretical ChemistryPorosityScalingThe Journal of Chemical Physics
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Conformational studies of bottle-brush polymers absorbed on a flat solid surface.

2010

The adsorption of a bottle-brush polymer end-grafted with one chain end of its backbone to a flat substrate surface is studied by Monte Carlo simulation of a coarse-grained model, that previously has been characterized in the bulk, assuming a dilute solution under good solvent conditions. Applying the bond fluctuation model on the simple cubic lattice, we vary the backbone chain length $N_b$ from $N_b=67$ to $N_b = 259$ effective monomeric units, the side chain length $N$ from N=6 to N=48, and the grafting density $\sigma=1$, i.e., parameters that correspond well to the experimentally accessible range. When the adsorption energy strength $\epsilon$ is varied, we find that the adsorption tra…

chemistry.chemical_classificationRange (particle radiation)Quantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodGeneral Physics and AstronomyBackbone chainThermodynamicsFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterGyrationCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerAdsorptionchemistrySide chainSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryThe Journal of chemical physics
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Theoretical study of the OH addition to the endocyclic and exocyclic double bonds of the d-limonene

2005

Abstract The initial step of the d-limonene + OH gas-phase reaction mechanism was investigated by means of ab initio calculations. We have considered eight different possibilities for the OH addition, corresponding to the two C–C double bonds, the two C atoms of each double bond, and the syn or anti orientation, with respect to the isopropenyl group (endocyclic attack) or the ring cycle (exocyclic attack). Activation energies calculated at the QCISD(T)/6-31G(d)//UMP2/6-31G(d) level, show that there are preferred orientations for the OH addition under atmospheric conditions of temperature and pressure.

chemistry.chemical_classificationReaction mechanismCrystallographyTemperature and pressureD limoneneDouble bondchemistryStereochemistryGroup (periodic table)Ab initio quantum chemistry methodsGeneral Physics and AstronomyPhysical and Theoretical ChemistryRing (chemistry)Chemical Physics Letters
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Experimental and theoretical investigations for the regio and stereoselective transformation of trans 1,2,3-trisubstituted aziridines into trans oxaz…

2003

The regio and stereoselective transformation of trans 1,2,3-trisubstituted aziridines into trans oxazolidin-2-ones takes place in good yield. However, the cis configuration at C2 and C3 in monocyclic aziridines is a limiting factor for this transformation. Ab initio calculations show that while the ring-opening process assisted by iodide is regioselective, the subsequent ring-closure is responsible for the retention of the configuration at the trans oxazolidin-2-ones. The larger energy found for the ring-closure process for the cis aziridines accounts for the non-formation of the cis oxazolidin-2-ones.

chemistry.chemical_classificationRegiochemistryStereochemistryOrganic ChemistryIodideStereoselective synthesisRegioselectivityBiochemistrychemistryAb initio quantum chemistry methodsYield (chemistry)Drug DiscoveryMolecular mechanismStereoselectivityCis–trans isomerismTetrahedron
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Polymer- and template-related factors influencing the efficiency in molecularly imprinted solid-phase extractions

1999

Abstract This review identifies the factors of importance in the development of molecularly imprinted polymers for use in solid-phase extractions and summarizes the results obtained to date in the area of bioanalysis, pharmaceutical analysis and environmental analysis.

chemistry.chemical_classificationRelated factorsBioanalysisChromatographychemistryEnvironmental analysisPhase (matter)Molecularly imprinted polymerSeparation methodPolymerSolid phase extractionSpectroscopyAnalytical ChemistryTrAC Trends in Analytical Chemistry
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On the calculation of free energy of mixing for aqueous polymer solutions with group-contribution models

2010

Abstract Liquid–liquid phase separation processes are currently used as a route to prepare polymeric porous structures for various applications (membranes and scaffolds for tissue engineering). In membrane and foam fabrication technologies, binary and mainly ternary polymer solutions are used. Membrane morphology is strongly affected by phase equilibria of processing solution. In order to achieve a better control of membrane morphology and to explore a wide quantity of solvents, a predictive tool addressing experimentals would be strongly advisable. In this paper, group contribution models were chosen to test the applicability on a PLLA–dioxane–water ternary polymer solution, whose experime…

chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaTernary numeral systemGeneral Chemical EngineeringLiquid–liquid equilibriaPhase separationSettore ING-IND/34 - Bioingegneria IndustrialeGeneral Physics and AstronomyMineralogyThermodynamicsPolymerEntropy of mixingGroup contribution methodPolymer solutionMembranechemistryPhase (matter)Group-contribution modelsPhysical and Theoretical ChemistryTernary operationMixing (physics)Fluid Phase Equilibria
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From orientational glasses to structural glasses: What computer simulations have contributed to understand experiments

2002

Abstract Orientational glasses, produced by random dilution of molecular crystals, exhibit a freezing transition of the quadrupole moments. Monte Carlo simulations of lattice models (generalization of the Edwards–Anderson spin glass model) have been used to elucidate this behavior. While short range models exhibit a static glass transition at zero temperature only, the infinite range Potts glass exhibits a transition where a glass order parameter appears discontinuously. At higher temperature, a dynamical transition occurs, described by mode-coupling theory (MCT). MCT has also been tested by Monte Carlo and molecular dynamics simulations of coarse-grained models of glass-forming polymers. W…

chemistry.chemical_classificationSpin glassCondensed matter physicsMonte Carlo methodPolymerCondensed Matter PhysicsCondensed Matter::Disordered Systems and Neural NetworksElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed MatterMolecular dynamicschemistryLattice (order)Materials ChemistryCeramics and CompositesGlass transitionAnderson impurity modelPotts modelJournal of Non-Crystalline Solids
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