Search results for "linear"

showing 10 items of 7165 documents

Double-quantum nutations in a two-level spin system

1986

The transient oscillatory behavior of the nonlinear response of a two-level electron-spin system is experimentally investigated in a sample of glassy silica with ${E}_{1}^{\mathcal{'}}$ centers (S=(1/2)) at microwave frequency at T=4.2 K. The transient regime, excited by an intense step-modulated radiation tuned to double-quantum (DQ) resonance, is monitored by revealing the second-harmonic (SH) wave radiated by the spins undergoing DQ transitions. Time- and frequency-domain results show that the emitted SH wave has two components: the former, which vanishes at the DQ resonance, exhibits an overdamped transient regime, the latter consists of damped oscillations at a frequency which depends …

chemistry.chemical_classificationPhysicsSpinsCondensed matter physicsChemistrySpin systemResonanceSemiclassical physicsGeneral ChemistryRadiationCondensed Matter PhysicsPolarization (waves)Nonlinear systemNuclear magnetic resonanceBloch equationsExcited stateMaterials ChemistryTransient (oscillation)IrradiationAtomic physicsInorganic compoundRabi frequencyPhysical Review B
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Polymer dynamics in time-dependent periodic potentials.

2008

Dynamics of a discrete polymer in time-dependent external potentials is studied with the master equation approach. We consider both stochastic and deterministic switching mechanisms for the potential states and give the essential equations for computing the stationary state properties of molecules with internal structure in time-dependent periodic potentials on a lattice. As an example, we consider standard and modified Rubinstein-Duke polymers and calculate their mean drift and effective diffusion coefficient in the two-state non-symmetric flashing potential and symmetric traveling potential. Rich non-linear behavior of these observables is found. By varying the polymer length, we find cur…

chemistry.chemical_classificationPhysicsStatistical Mechanics (cond-mat.stat-mech)Equations of stateFOS: Physical sciencesObservablemolekyylitPolymerFlashingNonlinear systemClassical mechanicschemistryLattice (order)Master equationMoleculepolymeeritCondensed Matter - Statistical MechanicsdynamiikkaPhysical review. E, Statistical, nonlinear, and soft matter physics
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Halogen bonding enhances nonlinear optical response in poled supramolecular polymers

2015

We demonstrate that halogen bonding strongly enhances the nonlinear optical response of poled supramolecular polymer systems. We compare three nonlinear optical chromophores with similar electronic structures but different bond-donating units, and show that both the type and the strength of the noncovalent interaction between the chromophores and the polymer matrix play their own distinctive roles in the optical nonlinearity of the systems. acceptedVersion Peer reviewed

chemistry.chemical_classificationPhysics::Biological PhysicsQuantitative Biology::BiomoleculesMaterials scienceHalogen bond116 Chemical sciencesGeneral ChemistryPolymerChromophorePolymers Supramolecular Chemistry Halogen Bonding Nonlinear Optical ResponseHalogen bonding; NLO; supramolecular polymers114 Physical sciencesSupramolecular polymersCondensed Matter::Soft Condensed MatterOptical nonlinearityNonlinear opticalchemistryChemical physicsPolymer chemistryMaterials ChemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysics::Chemical Physics
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Basic kinetic model for the reaction yielding linear polyurethanes. II

1995

On the basis of the gradual polyaddition kinetic model developed earlier, an attempt was made to provide a generalized mathematical model for the set of reactions yielding linear polyurethanes. The model is a system of first-order ordinary differential equations. It was assumed at the present stage of this model that the rate constants for the reaction considered do not change. The model developed was then solved numerically. Average molecular weight of the polymer and composition data for oligomers were calculated for a constant volume batch reactor and varied process parameters. The GPC method, which was tested for model urethane oligomers, was employed to verify the model developed. The …

chemistry.chemical_classificationPolymers and PlasticsBasis (linear algebra)Batch reactorThermodynamicsGeneral ChemistryPolymerSurfaces Coatings and FilmsReaction rate constantchemistryChain (algebraic topology)Ordinary differential equationPolymer chemistryMaterials ChemistryMolar mass distributionConstant (mathematics)Journal of Applied Polymer Science
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Calculation of vapor pressures not requiring the derivatives of the energy of mixing

1997

A method is presented for the calculation of vapor pressures exclusively on the basis of the energy of mixing, the knowledge of chemical potentials is not required. The only condition used for the calculation is the minimum of the energy of mixing of the overall system in equilibrium. The gas phase is treated as an ideal gas, for the liquid phase no specific thermodynamic description is assumed. The method is demonstrated for a mixture of two solvents and one polymer. The system water/poly(ethylene oxide), the thermodynamics of which are described by an equation that can only be solved numerically thus impeding the calculation of chemical potentials, serves as an example. Interaction parame…

chemistry.chemical_classificationPolymers and PlasticsBasis (linear algebra)Ethylene oxideOrganic ChemistryLiquid phaseThermodynamicsPolymerCondensed Matter PhysicsIdeal gasGas phaseInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryMixing (physics)Energy (signal processing)Macromolecular Theory and Simulations
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1981

Theoretical predictions from a non-linear model based on the free volume concept, which were previously tested only with a molten polymer, are presented and compared with literature data of solid polyethylene. The agreement is good both when a steady state is reached in the experimentally explored times and when, on the contrary, the data do not show it. Theoretische Berechnungen des elektrischen Verhaltens von Polymeren anhand eines nichtlinearen Modells, die auf dem Konzept des freien Volumens basieren und bisher lediglich an einem geschmolzenen Polymer getestet wurden, werden vorgestellt und mit Literaturdaten von festem Polyethylen verglichen. Die Ubereinstimmung ist gut, wenn in den ex…

chemistry.chemical_classificationPolymers and PlasticsChemistryGeneral Chemical EngineeringThermodynamicsNon linear modelPolymerActa Polymerica
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Electron crystallography and organic materials with non-linear optical properties

1999

Results of electron microscopic studies of crystal structures of a number of bis-benzylidene cyclohexanones are presented. It is shown that some of these compounds are efficient crystalline non-linear optically active (NLO) chromophores with second harmonic generation (SHG) properties. Appropriately functionalized chromophores of this type can be used as a polycondensation comonomer to produce partly crystalline main-chain NLO-active polymers. Electron diffraction crystal structural data, obtained for very small crystals, allowed us to get reasonable estimations of macroscopic crystal NLO-coefficients, relating quantum-chemically calculated molecular first hyperpolarizability components to …

chemistry.chemical_classificationPolymers and PlasticsElectron crystallographyOrganic ChemistryPhysics::OpticsHyperpolarizabilitySecond-harmonic generationNonlinear opticsPolymerCrystal structureCondensed Matter PhysicsCrystalCrystallographyElectron diffractionchemistryMaterials ChemistryMacromolecular Symposia
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Single molecule probing of dynamics in supercooled polymers

2011

6 pages; International audience; Fluorescence experiments with single BODIPY molecules embedded in a poly(methyl acrylate) matrix have been performed at various temperatures in the supercooled regime. By using pulsed excitation, fluorescence lifetime and linear dichroism time trajectories were accessible at the same time. Both observables have been analyzed without data binning. While the linear dichroism solely reflects single particle dynamics, the fluorescence lifetime observable depends on the molecular environment, so that the dynamics from the polymer host surrounding a chromophore contributes to this quantity. We observe that the lifetime correlation decays slightly faster than polar…

chemistry.chemical_classificationPolymersAnalytical chemistryGeneral Physics and Astronomy02 engineering and technologyPolymerChromophoreDichroism010402 general chemistry021001 nanoscience & nanotechnologyPolarization (waves)Linear dichroism01 natural sciencesFluorescence0104 chemical scienceschemistry.chemical_compound[CHIM.POLY]Chemical Sciences/PolymerschemistryChemical physicsMoleculePhysical and Theoretical ChemistryBODIPY0210 nano-technologySingle BODIPY moleculesExcitation
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Mean square radius of gyration and hydrodynamic radius of jointed star (dumbbell) and H-comb polymers

1996

Equations for the mean square radius of gyration and the hydrodynamic radius for jointed stars (dumbbells) and H-combs are derived, based on random flight statistics for each subchain. Comparision with literature data on computer simulations and experimental data for H-combs show good agreement for the g-value of the mean square radius of gyration even in good solvents. This suggests that for the mean square radius of gyration the relative dimension of a H-comb relative to the linear molecule of the same degree of polymerization is not altered significantly by long range interactions, as in the case of star polymers. For the hydrodynamic radius the situation is different. Fair agreement is …

chemistry.chemical_classificationQuantitative Biology::BiomoleculesHydrodynamic radiusPolymers and Plasticsbusiness.industryChemistryOrganic ChemistryLinear molecular geometryPolymerDegree of polymerizationCondensed Matter PhysicsRelative dimensionMolecular physicsCondensed Matter::Soft Condensed MatterInorganic ChemistryViscosityOpticsMaterials ChemistryRadius of gyrationDumbbellbusinessMacromolecular Theory and Simulations
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Carboxylation of a linear low density polyethylene via gamma irradiation in presence of carbon dioxide in subcritical and supercritical conditions

1994

Abstract In this work the molecular modifications induced in a linear low density polyethylene gamma irradiated in presence of carbon dioxide both in subcritical and supercritical conditions are presented. The obtained results indicate that this process can be a new and interesting way in order to graft oxidized groups in the polyethylene chains. Moreover it is worth noting that, together with these functionalization reactions, also a significant crosslinking occurs, with improvement in some mechanical tensile behaviour.

chemistry.chemical_classificationRadiationMaterials sciencePolymerPolyethyleneSupercritical fluidLinear low-density polyethylenechemistry.chemical_compoundchemistryPolymerizationCarboxylationChemical engineeringCarbon dioxideCompounds of carbonNuclear chemistryRadiation Physics and Chemistry
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