Search results for "Liquid crystalline"

showing 10 items of 85 documents

Thermal Analysis, Mechanical and Rheological Behaviour of Melt Manufactured Polyethylene/Liquid Crystal Polymer Blends

2011

Modification of properties of conventional thermoplastics with thermotropic liquid crystal polymers, from one hand, allows decrease their viscosities, substantially facilitating processing conditions, and, from another hand, allows increase their exploitation properties. Orientation of the labile structure of liquid crystal polymer in extrusion or injection moulding causes specific reinforcement (so-called self-reinforcement) to occur in the blends containing liquid crystal polymer. Up to now the effect of self-reinforcement is mostly investigated in the blends, containing considerable amount of liquid crystal polymer. In this research the effect of minor amounts of liquid crystalline co-po…

chemistry.chemical_classificationpolyethylenelcsh:TN1-997Hydroxybenzoic acidMaterials scienceThermoplasticthermotropic liquid crystalline polymersynthesisPolymerPolyethyleneThermotropic crystalchemistry.chemical_compoundrheological propertieschemistryLiquid crystalUltimate tensile strengthGeneral Materials ScienceInjection mouldingstructuremechanicalComposite materiallcsh:Mining engineering. MetallurgyMedžiagotyra
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Synthesis of PP-LCP graft copolymers and their compatibilizing activity for PP/LCP blends

1998

The aim of this work was the synthesis of new graft copolymers consisting of polypropylene (PP) backbones and liquid crystalline polymer (LCP) branches, to be used as compatibilizing agents for PP/LCP blends. The PP-g-LCP copolymers have been prepared by polycondensation of the monomers of a semiflexible liquid crystalline polyester (SBH 1 : 1 : 2), that is, sebacic acid (S), 4,4′-dihydroxybiphenyl (B), and 4-hydroxybenzoic acid (H) in the mole ratio of 1 : 1 : 2, carried out in the presence of appropriate amounts of a commercial acrylic-acid-functionalized polypropylene (PPAA). The polycondensation products, referred to as COPP50 and COPP70, having a calculated PPAA concentration of 50 and…

PolypropyleneMaterials scienceCondensation polymerPolymers and PlasticsSebacic acidCopolymersGeneral ChemistryCompatibilizationFunctionalized polypropyleneSurfaces Coatings and FilmsPolypropylene-LCP blendsPolyesterchemistry.chemical_compoundDifferential scanning calorimetryLiquid crystalline polymer (LCP)chemistryTacticityPolymer chemistryMaterials ChemistryCopolymerCompatibilization
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Growth of large liquid crystalline domains of phospholipids at air-water interfaces

1990

Abstract The fusion of condensed phase domains in a fluid environment in monolayers is studied. A system of electrodes permits the non-invasive and predetermined movement of single domains while the film is observed by fluorescence microscopy. Two domains fuse when they are brought into contact with special positions of their borderlines. The experiment yields information about the molecular structure of the domains and allows us to fabricate very large domains. The equilibrium size is estimated and verified.

Fusionbusiness.industryLiquid crystallineChemistryMetals and AlloysSurfaces and InterfacesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOpticsChemical physicsLiquid crystalPhase (matter)MonolayerElectrodeMaterials ChemistryMoleculeAir waterbusinessThin Solid Films
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Polymers with Side-chain Mesogenic Units

1989

Liquid crystalline (LC) polymers are usually prepared by combining formanisotropic structural units (so-called mesogenic groups) and polymer chains (Figure 1). The mesogenic groups used for this purpose are rigid rod-like or disc-like units, which are known to favour LC phases in the case of low molar mass substances. There are two main ways of combining the mesogenic groups and polymer chains. The mesogenic groups can either be incorporated actually into the polymer chains (LC main-chain polymers, see Volume 5, Chapter 38) or they can be attached to flexible polymer chains as side groups (LC side-chain polymers).

chemistry.chemical_classificationMolar massMaterials sciencechemistryLiquid crystallineMesogenPolymer chemistrySide chainPolymer
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1985

Etude des phases isotrope, nematique et smectique de melanges de polymeres protones et en partie deuteries

chemistry.chemical_classificationCrystallographyDeuteriumChemistryLiquid crystallineLiquid crystalPolymerNeutron scatteringDie Makromolekulare Chemie, Rapid Communications
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Combined main chain/side chain polymers. A new class of liquid crystalline polymers with unusual structural, thermodynamic and dynamic properties

1990

Abstract Combined main chain/side chain polymers carry rigid rod-like mesogenic units both in the side chain and along the chain backbone. The properties of such combined systems are expected to be controlled by the competition of the interactions between the mesogenic units in the side and main chains as well as the tendency of the chain backbones to maximize their entropy. The thermodynamic, structural and dynamic properties of such combined main chain/side chain liquid-crystalline polymers were investigated for various chain architectures. The combined systems were found to display properties corresponding in many cases to a favourable superposition of properties characteristic of both m…

chemistry.chemical_classificationMaterials scienceLiquid crystallineMesogenThermodynamicsGeneral ChemistryPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterSuperposition principlechemistryLiquid crystalSide chainOrganic chemistryGeneral Materials ScienceEntropy (order and disorder)Liquid Crystals
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Functional Liquid Crystalline Polymers: Ferroelectric Polymers and Liquid Crystalline Elastomers and Ionomers

1994

Abstract The incorporation of different functional groups in liquid crystalline polymers opens the way to a variety of interesting new materials, which may be used for non-linear optics, as piezo-elements or as two-phasic composite materials.

chemistry.chemical_classificationMaterials scienceFerroelectric polymersLiquid crystallinePolymerCondensed Matter PhysicsElastomerFerroelectricitychemistry.chemical_compoundchemistryChemical engineeringLiquid crystalFunctional groupPolymer chemistryIonomerMolecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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1978

Biphenylchemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryGroup (periodic table)Liquid crystallineMesogenPolymer chemistryPolymerDie Makromolekulare Chemie
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Enantiodifferentiation of acyclic phosphonium salts in chiral liquid crystalline solutions

2006

Abstract The enantiodifferentiation of acyclic phosphonium salts bearing a stereogenic centre, whether on the phosphorus atom or on one of its substituents, was investigated by 2 H–{ 1 H}, 13 C–{ 1 H} and 31 P–{ 1 H} NMR in chiral liquid crystals composed of a polypeptide dissolved in an organic solvent. For the first time, the enantiomers of P-chirogenic phosphorus compounds were discriminated in these anisotropic media, affording good to excellent separation of the signals, allowing the determination of their proportion. While 31 P–{ 1 H} NMR spectra showed no chiral separation, 2 H–{ 1 H} NMR was efficient in the enantiodifferentiation of an isotopically labelled compound. Better still, …

Alternative methodsChemistryLiquid crystallineOrganic ChemistryCarbon-13 NMRCatalysisStereocenterInorganic ChemistryNMR spectra databasechemistry.chemical_compoundCrystallographyLiquid crystalOrganic chemistryPhosphoniumPhysical and Theoretical ChemistryEnantiomerTetrahedron: Asymmetry
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Strain‐induced compression of smectic layers in free‐standing liquid crystalline elastomer films

2005

The deformation of oriented smectic liquid crystal elastomer films with smectic layers parallel to the film surface was studied using optical reflectometry and small angle X‐ray diffraction. Reflectometry data show that in the chosen material, in‐plane strain causes a change in the optical thickness of the free‐standing films. Small angle X‐ray scattering was used to explore the molecular origin of this effect. The X‐ray scattering data confirm that the change in optical thickness originates from the compression of the individual smectic layers. The measured Poisson ratio in the smectic A and C* phases is close to ½, in contrast to the smectic elastomers investigated earlier by Nishikawa et…

DiffractionMaterials scienceCondensed matter physicsScatteringbusiness.industryLiquid crystallineGeneral ChemistryCondensed Matter PhysicsElastomerPoisson's ratioCondensed Matter::Soft Condensed MatterCondensed Matter::Materials Sciencesymbols.namesakeOpticsLiquid crystalLattice (order)symbolsGeneral Materials SciencebusinessReflectometryLiquid Crystals
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