Search results for "Chemical physics"

showing 10 items of 2553 documents

Semidilute and Concentrated Polymer Solutions near Attractive Walls:  Dynamic Monte Carlo Simulation of Density and Pressure Profiles of a Coarse-Gra…

1997

Using a bead−spring model of flexible polymer chains, we study polymer adsorption from solutions onto attractive planar walls, varying both the strength of the adsorption potential e and the concentration of the solution over a wide range. Treating the case of good solvents, the profiles of density and pressure are computed and it is shown that thermal equilibrium between the adsorbed layer and the bulk solution is obtained. The case of a wall with purely repulsive potential under otherwise identical conditions is treated for comparison. It is shown that for the strongly adsorbing wall there is a pronounced layering, while a layered structure at the repulsive wall occurs only for high conce…

chemistry.chemical_classificationThermal equilibriumPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodPolymerPolymer adsorptionSurface energyCondensed Matter::Soft Condensed MatterInorganic ChemistryAdsorptionChemical physicsMaterials ChemistryStatistical physicsTotal pressureLayeringMacromolecules
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Frontispiece: Hierarchy of Asymmetry at Work: Chain-Dependent Helix-to-Helix Interactions in Supramolecular Polymers

2018

chemistry.chemical_classificationWork (thermodynamics)Hierarchy (mathematics)media_common.quotation_subjectOrganic ChemistryGeneral ChemistryHelicityAsymmetryCatalysisSupramolecular polymersSelf sortingchemistryChain (algebraic topology)Chemical physicsHelixmedia_commonChemistry - A European Journal
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Cover Feature: Towards Atomically Precise Supported Catalysts from Monolayer‐Protected Clusters: The Critical Role of the Support (Chem. Eur. J. 31/2…

2020

chemistry.chemical_classificationX-ray absorption spectroscopyChemistryChemical physicsFeature (computer vision)Organic ChemistryMonolayerNon-covalent interactionsCover (algebra)General ChemistryCatalysisCatalysisChemistry – A European Journal
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Surface and bulk ordering in thin films of a symmetrical diblock copolymer

2013

Amphiphilic diblock copolymers have the ability to adapt their surface's molecular composition to the hydrophilicity of their environment. In the case of about equal volume fractions of the two polymer blocks, the bulk of these polymers is known to develop a laminar ordering. We report here our investigation of the relationship between bulk ordering and surface morphology/chemical composition in thin films of such an amphiphilic diblock copolymer. Upon annealing in vacuum, the expected lamella ordering in the bulk of the film is observed and we find the morphology of the film surface to be defined by the thickness of the as-deposited film: If the as-deposited thickness matches the height of…

chemistry.chemical_classification[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Materials sciencePolymers and PlasticsAnnealing (metallurgy)Laminar flowPolymerCondensed Matter PhysicschemistryPolymer chemistryAmphiphileMaterials ChemistryCopolymer[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryThin filmComposite materialGlass transition[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]Chemical compositionJournal of Polymer Science Part B: Polymer Physics
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Precise structural investigation of symmetric diblock copolymer thin films with resonant soft X-ray reflectivity

2013

Symmetric diblock copolymers are known to form lamellar structures in the bulk of an organic thin film. Polymer/polymer and polymer/substrate interfaces play a critical role in this application. Here, we report the investigation of multiple buried interfaces by using a novel technique resonant soft X-ray reflectivity which benefits from enhanced contrast between different polymers near the carbon K-edge. This allows us to obtain a precise interface structure. We also present an alternative method to determine optical constants of polymers by fitting X-ray reflectivity of polymers with known structural parameters at specific soft X-ray energies. This approach is compared with the way of obta…

chemistry.chemical_classification[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Materials sciencechemistry.chemical_elementGeneral ChemistrySubstrate (electronics)PolymerCondensed Matter PhysicsMolecular physicsXANESCrystallographychemistryCopolymerLamellar structure[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Thin filmRefractive indexCarbon[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]
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Stability of the functional NLO polymers–optically induced depoling of the DMABI molecules in sPMMA matrix

2008

Abstract Low polar order (PO) stability is the major problem of the polymer materials for nonlinear optical (NLO) applications. In this contribution we will show the results of PO stability investigations in the corona poled 3 wt.% DMABI + sPMMA guest–host system. Influence of the poling temperature on the building and stability of the polar order in the system will be presented. To characterize the stability, PO destruction has been caused by high intensity light. Polar order stability characteristics were obtained from the sample second harmonic generation intensity (SHI) time decays. We have found that the decay signal is the best fit to the sum of two exponentials. Several physical mode…

chemistry.chemical_classificationbusiness.industryChemistryKineticsPolingMetals and AlloysSecond-harmonic generationNonlinear opticsSurfaces and InterfacesPolymerCorona polingSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOpticsChemical physicsMaterials ChemistryPolarMoleculebusinessThin Solid Films
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Strong Field Iron(II) Complex Converted by Light into a Long-Lived High-Spin State

2000

chemistry.chemical_classificationchemistrySpin statesChemical physicsInorganic chemistryStrong fieldGeneral ChemistryCatalysisCoordination complexAngewandte Chemie
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Single Particle Motion of Hard-Sphere-Like Polymer Micronetwork Colloids Up to the Colloid Glass Transition

1997

Polymer micronetwork spheres swollen in a good solvent can be regarded as colloids which require no special stabilisation to avoid aggregation. Their interactions can be timed by changing the degree of internal crosslinking. The phase behaviour and the static structure factor demonstrate that crosslink density of 1:10 (inverse number of monomer units between crosslinks) is sufficient to achieve hard sphere behaviour. We designed a host-tracer system consisting of core-shell micronetwork spheres (core: polystyrene; shell: poly-t-butylacrylate) in a host of refractive-indexmatched poly-t-butylacrylate micronetwork colloids. Employing a crosslink density of 1:10 and tuning the polydispersity s…

chemistry.chemical_classificationchemistry.chemical_compoundColloidMaterials sciencechemistryDynamic light scatteringChemical physicsPhase (matter)DispersityPolymerPolystyreneGlass transitionStructure factor
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QENS from polymeric micelles in supercritical CO[sub 2]

2000

We report QENS measurements from PS-b-PFOA aggregates in supercritical CO2. These consist of dense cores of CO2-insoluble polystyrene surrounded by a ‘corona’ of PFOA surfactant molecules whose CO2-philic groups interface with supercritical CO2. Lineshapes are dominated by localized diffusive modes and segmental dynamics of the anchored, finite-length PFOA chains. For Q∼0.6 A−1, we obtain effective diffusion coefficients of ≈0.8×10−6 cm2/sec. At higher Q, a single component is not sufficient as shown by excess intensity on the flanks. For Q>1.5 A−1, the wings reflect contributions due to a distribution of faster, more localized chain modes.

chemistry.chemical_classificationchemistry.chemical_compoundCrystallographychemistryChemical physicsDiffusionMoleculePolymerPolystyreneCrystal structureNeutron scatteringSupercritical fluidPhase diagramAIP Conference Proceedings
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RELAXATION METHODS FOR STUDYING MACROMOLECULAR MOTION IN THE BULK

1982

Abstract Macromolecular motion in amorphous and partially crystalline polymers is discussed in the light of recent relaxation experiments with particular emphasis on NMR methods. Polystyrene and polyethylene serve as pertinent examples where a considerable amount of new experimental data provides a bysis for better understanding molecular processes below and above the glass transition, and in the melt.

chemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryChemical physicsRelaxation (iterative method)Organic chemistryPolymerPolystyrenePolyethyleneGlass transitionMacromoleculeAmorphous solid
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