Search results for "Phase"

showing 10 items of 6344 documents

Dicyanobenzothiadiazole Derivatives Possessing Switchable Dielectric Permittivities

2017

Benzothiadiazoles are important electron acceptors and are frequently employed as electron-deficient components of donor-acceptor polymers. We report the effect of nitrile functionalities on the reactivity, steric hindrance, optoelectronic properties, and dielectric permittivity in dicyanobenzothioadiazole (DCNBT). Dielectric spectroscopy in the bulk and in solution assisted by DFT-calculations revealed that these molecules can be engineered to engender maximum values of the dipole moment and of dielectric permittivity due to the strong electron-withdrawing effect of the nitrile groups. The self-assembly in the bulk was investigated by X-ray scattering performed on single crystals, fibers (…

chemistry.chemical_classificationMaterials scienceNitrileRelative permittivity02 engineering and technologyPolymerDielectric010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesDielectric spectroscopyDipolechemistry.chemical_compoundchemistryChemical physicsLiquid crystalPhase (matter)Organic chemistryGeneral Materials Science0210 nano-technologyACS Applied Materials & Interfaces
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Sanidics: A new class of mesophases, displayed by highly substituted rigid-rod polyesters and polyamides

1990

Abstract The structure of rigid-chain polyesters and polyamides which possess flexible side chains consisting of methylene or 1,4,7-trioxaoctyl oxide units have been investigated by means of X-ray scattering. The X-ray studies were performed on fibres and monodomains. Additional information was gained from calorimetric, dilatometric and microscopic studies. The investigations revealed that these polymers display mesophases and that the structures of the mesophases differ from those observed for discotic and calamitic phases. They are characterized by the fact that in the ordered and disordered phases board-like molecules are stacked parallel on top of each other and that these stacks of mol…

chemistry.chemical_classificationMaterials scienceOxideGeneral ChemistryPolymerCondensed Matter PhysicsPolyesterCrystallographychemistry.chemical_compoundchemistryLiquid crystalPhase (matter)PolyamideSide chainMoleculeOrganic chemistryGeneral Materials ScienceLiquid Crystals
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Simulation of Dense Polymer Systems in Two and Three Dimensions

1991

Dense polymer systems are modeled by self- and mutually avoiding walks on lattices. Both simple models where the step length is one lattice spacing and more complicated models where the step length is distinctly longer and may fluctuate (“bond fluctuation model”) are discussed, and it is shown that the computer simulation of such models gives useful insight to understand the thermodynamic phase behavior and the relaxational dynamics of dense polymer solutions and polymer melts. The huge demands in computing power needed for a successful simulation of such systems can be covered by parallel computers such as the multitransputer facility of the University of Mainz.

chemistry.chemical_classificationMaterials sciencePhase (waves)General Physics and AstronomyStatistical and Nonlinear PhysicsPolymerStride lengthComputer Science ApplicationsPower (physics)Lattice constantComputational Theory and MathematicschemistrySimple (abstract algebra)Statistical physicsBond fluctuation modelMathematical PhysicsInternational Journal of Modern Physics C
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Photoresponsive Ferroelectric Liquid-Crystalline Polymers

2007

The photoresponse of ferroelectric smectic side-chain liquid-crystalline (LC) polymers containing a photoisomerizable azobenzene derivative as a covalently linked photochromic side group is investigated. By static measurements in different photostationary states, the effect of trans-cis isomerization on the material's phase-transition temperatures and its ferroelectric properties (spontaneous electric polarization Ps and director tilt angle 0) are analyzed. It turns out that the Curie temperature (transition S C * to S A ) can be reversibly shifted by up to 17 °C. The molecular mechanism of this "photoferroelectric effect" is studied in detail using time-resolved measurements of the dye's o…

chemistry.chemical_classificationMaterials sciencePolymerCondensed Matter PhysicsPhotochemistryFerroelectricityElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundPhotochromismPolarization densityAzobenzenechemistryPhase (matter)ElectrochemistryOrganic chemistryCurie temperatureIsomerizationAdvanced Functional Materials
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Blends from redox active liquid crystal ionomers and amorphous ionomers

1994

Abstract Biphasic blends (mixtures) of liquid crystal ionomers (prepared from ferrocene containing liquid crystal polymers by a redox reaction) and partially sulfonated polystyrene combine the constituent properties in a way, which is dependent on the measuring method. Polarizing microscopy shows homogenous textures similar to the pure liquid crystal polymer. Mechanical measurements show however the elastomeric behaviour of sulfonated polystyrene. The phase separated structure of these blends is proved by differential scanning calorimetry measurements.

chemistry.chemical_classificationMaterials sciencePolymerGeneral ChemistryElastomerCondensed Matter PhysicsAmorphous solidchemistry.chemical_compoundDifferential scanning calorimetryFerrocenechemistryChemical engineeringLiquid crystalPhase (matter)Organic chemistryGeneral Materials SciencePolystyreneLiquid Crystals
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Discotic liquid crystals at the air water interface

1991

The monolayer properties of two types of discotic liquid crystals, hexasubstituted triphenylenes 1 and azo derivatives of phloroglucinol 5, were examined. First investigations show that these discotic liquid crystals form stable monolayers. It could be shown that electron acceptors insert into the monolayer of 1. Azo discs display a packing behaviour at the monolayer that is ascribed to a side-on packing of the molecules.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsAir water interfaceDiscotic liquid crystalOrganic ChemistryElectron acceptorCondensed Matter PhysicsCrystallographychemistryMonolayerMaterials ChemistryOrganic chemistryMoleculeColumnar phaseMakromolekulare Chemie. Macromolecular Symposia
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Impact of Amino-Functionalization on the Response of Poly(ethylene glycol) (PEG) to External Stimuli

2022

It is shown that amino-functionalization of poly(ethylene glycol) (PEG) with the comonomer N,N-diethyl glycidyl amine (DEGA) triggers the emergence of extraordinary stimuli responsiveness and phase behavior of PEG. In dependence of the solution pH, tapered PEG-co-PDEGA exhibits a highly cooperative two-step inverse phase transition with respect to temperature. The polymer forms dispersed metastable nanoglobules in the medically relevant temperature range around human body temperature. Independently, cloud points can be adjusted between 40 and 90 °C via the pH of the solution. Changing the polymer architecture to a block structure, in pronounced contrast, the polymer exhibits a gradual growt…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsComonomerOrganic ChemistryPolymer architecturePolymerAtmospheric temperature rangeMicelleInorganic Chemistrychemistry.chemical_compoundChemical engineeringchemistryPhase (matter)PEG ratioPolymer chemistryMaterials ChemistryEthylene glycolACS Macro Letters
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Large Scale Fractionation of Macromolecules

2004

Access to sufficiently large amounts of material with adequate molecular and chemical uniformity from polydisperse natural products or synthetic materials has been a long-standing challenge to polymer scientists. We have developed a broadly applicable preparative fractionation method consisting of a special kind of continuous extraction removing the easier soluble components from the initial product. It is rendered possible by the use of spinning nozzles throught which a concentrated polymer solution is pressed into a liquid of tailored thermodynamic quality. The initially produced jets of the source phase disintegrate rapidly into minute droplets of typically 50 μm diameter. This efficient…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringScale (chemistry)Organic ChemistryExtraction (chemistry)Analytical chemistryFractionationPolymerSynthetic materialsChemical engineeringchemistryPhase (matter)Materials ChemistrySpinningMacromoleculeMacromolecular Materials and Engineering
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Indentation test as a tool for monitoring the solidification process during injection molding

2003

An inline method for monitoring the solidification process during the injection molding of semicrystalline polymers is demonstrated. The method has been applied to various poly(ethylene terephthalate) (PET) and poly(buthylene terephthalate) (PBT) samples. The technique is based on a simple device by which an additional ejector pin is pushed onto the injection-molded part with a fixed force at different times during the solidification phase while the mold remains closed. The residual deformation (the so-called indentation depth) due to the applied load is measured offline after ejection. By the performance of indentation at different times during the cooling phase, an indentation depth profi…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsGlass fiberGeneral ChemistryInjectorMolding (process)Polymermedicine.disease_causeSurfaces Coatings and Filmslaw.inventionchemistrylawIndentationPhase (matter)MoldMaterials ChemistrymedicineComposite materialCrystallizationJournal of Applied Polymer Science
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Effect of adding new phosphazene compounds to poly(butylene terephthalate)/polyamide blends. II: Effect of different polyamides on the properties of …

2006

Poly(butylene terephthalate) (PBT) and a sample of polyamide have been melt processed in the presence of two new phosphazene compounds, namely 2,2-dichloro-4,4,6,6-bis[spyro(2',2"-dioxy-1',1"-biphenyl)]cyclotriphosphazene (2Cl-CP) and 2,2-bis(2-methoxy-4-methyleneoxy-phenoxy)-4,4,6,6-bis[spyro(2',2"-dioxy-1',1"-biphenyl)]cyclophosphazene (CP-2EPOX). The blends were prepared by using polyamide 6 (PA6) and polyamide 6,6 (PA66) in 25/75 and 75/25 w/w compositions by using a co-rotating twin-screw extruder. The materials have been completely characterized from a mechanical, rheological, and morphological point of view. The results indicate that the additives used cause an increase of the ruptur…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsIzod impact strength testPolymerCompatibilizationPolymer blendCondensed Matter PhysicsCyclophosphazeneReactive compatibilizationchemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryPoly(butylene terephthalate)Mechanics of MaterialsPhase (matter)Polymer chemistryPolyamideMaterials ChemistryCopolymerPolyamidePolymer blendPhosphazene
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