Search results for "liquid"

showing 10 items of 4351 documents

1986

Preparation d'oligosiloxanes et de polyarylates avec des groupes mesogenes fixes lateralement

chemistry.chemical_classificationPhase transitionchemistry.chemical_compoundChain (algebraic topology)ChemistryLiquid crystallineLiquid crystalPolymer chemistryPolymerPendant groupOligomerDie Makromolekulare Chemie, Rapid Communications
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Effect of traditional, microwave and industrial cooking on inositol phosphate content in beans, chickpeas and lentils

2003

An high-performance liquid chromatography method for determining inositol phosphate fractions was adapted to legumes. The validity of the method was assessed by estimating the following analytical parameters: linearity (linear response between 125 and 5000 microg inositol hexaphosphate (IP(6))/ml); instrumental precision and method precision (relative standard deviation, %) were 1.9% (IP(6)) for instrumental, and 2.5% (IP(6)) and 8.2% (IP(5)) for method precision. An accuracy was estimated by percentage recovery (72 +/- 3%). The application of this method to raw, conventional, microwave-cooked and ready-to-eat beans, chickpeas and lentils gave IP(6) contents ranging from 0.63 g/100 g dry ma…

chemistry.chemical_classificationPhytic AcidFood HandlingInositol PhosphatesRelative standard deviationReproducibility of ResultsFabaceaeCicerBioavailabilityInositol pentaphosphatechemistryBotanyLens PlantDry matterInositol hexaphosphateFood scienceMicrowavesInositol phosphateChromatography High Pressure LiquidLegumeFood ScienceInternational Journal of Food Sciences and Nutrition
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1989

A series of combined main-chain side-group liquid-crystalline polymers was synthesized by melt polycondensation from trans-1,4-cyclohexanedicarboxylic acid, chloro-1,4-phenylene diacetate and 6-(4-methoxy-4′-biphenylyloxy)hexyl-1,4-phenylene diacetate. These polyesters combine the features of rigid-rod main-chain LC-polymers and of side-group LC-polymers. Polymers with small fractions of mesogenic side-groups (5 and 10 mol-%) have lower melting points than the parent polymer poly(chloro-1,4-phenylene 1,4-cyclohexanedicarboxylate) but are still liquid crystalline up to their decomposition at T ≥ 400°C. In polymers with larger fractions of mesogenic side-groups (50 and 100 mol-%) partial isom…

chemistry.chemical_classificationPolyesterCondensation polymerMaterials sciencechemistryLiquid crystalMesogenPolymer chemistryMelting pointThermomechanical analysisPolymerDynamic mechanical analysisDie Makromolekulare Chemie
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1983

The synthesis and the phase behaviour of liquid crystalline main chain polymers are described. In these poly- and copolyesters the mesogenic units are linked by highly flexible oligodimethylsiloxane spacers. The comparison of their phase behaviour with that of polyesters known from the literature shows that dimethylsiloxane spacers as a replacement for alkyl spacers are leading to a drastic decrease of the transition temperatures. Depending on the length of the spacer glass transitions as low as −111°C can be achieved. The widths of the liquid crystalline phases thereby are retained up to a spacerlength of 13 oxydimethylsilanediyl (dimethylsiloxane) units. The homopolyesters mainly show sme…

chemistry.chemical_classificationPolyesterchemistry.chemical_compoundMaterials sciencechemistryLiquid crystalMesogenPhase (matter)SiloxanePolymer chemistryPolymerAtmospheric temperature rangeAlkylDie Makromolekulare Chemie
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Supramolecular Thermotropic Liquid Crystalline Materials with Nematic Mesophase Based on Methylated Hyperbranched Polyethylenimine and Mesogenic Carb…

2006

Supramolecular interaction of fully methylated hyperbranched polyethylenimines (PEI) with a mesogen-based carboxylic acid, 5-(p-cyanobiphenoxy)pentanoic acid, results in the formation of supramolecular complexes exhibiting thermotropic liquid crystalline (LC) mesophases. In contrast to the common smectic mesophases of most dendritic LC polymers, nematic LC phase were observed. The complexation of PEI and the mesogen units is due to electrostatic interaction between the carboxylate groups and the ammonium end groups of PEI. LC properties were investigated by a combination of differential scanning calorimetry, polarizing light optical microscopy, and X-ray diffractometry.

chemistry.chemical_classificationPolyethylenimineMaterials sciencePolymers and PlasticsMesogenCarboxylic acidOrganic Chemistrytechnology industry and agricultureSupramolecular chemistryMesophasemacromolecular substancesThermotropic crystalchemistry.chemical_compoundchemistryLiquid crystalPolymer chemistryMaterials ChemistryCarboxylateMacromolecular Rapid Communications
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Towards storage-stable high-content recycled tyre rubber modified bitumen

2018

The addition of crumb rubber particles as bitumen modifier can be currently considered as a well-established alternative to conventional polymers for bitumen modification. However, Recycle Tyre Rubber (RTR) modified binders still present drawbacks such as poor mix workability and hot storage stability. Within this study the authors try unlocking the full potential of devulcanised tyre rubber-heavy oils blend, named Liquid Rubber (LR), by exploring the possibility of tailoring recycled polymer modified bitumen with unconventional high-content of RTR and designed to overcome the above mentioned technological problems of RTR modified bitumen while keeping its advantages. Results show that LR-b…

chemistry.chemical_classificationPolymer modifiedMaterials science0211 other engineering and technologies02 engineering and technologyBuilding and ConstructionPolymer021001 nanoscience & nanotechnologyrecycled tyre rubber Liquid rubber bitumen modification storage stability asphalt rubber no-agitation wet processNatural rubberRheologychemistryAsphaltvisual_artLiquid rubber021105 building & constructionvisual_art.visual_art_mediumGeneral Materials ScienceCrumb rubberComposite materialSolubility0210 nano-technologyCivil and Structural EngineeringConstruction and Building Materials
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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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Biphasic ethylene polymerisation using 1-n-alkyl-3-methylimidazolium tetrachloroaluminate ionic liquid as a medium of the Cp2TiCl2 titanocene catalyst

2008

Abstract A systematic analysis was performed on a series of 1- n -alkyl-3-methylimidazolium tetrachloroaluminates (where alkyl = ethyl, butyl, hexyl, and octyl), applied as a medium of the Cp 2 TiCl 2 titanocene catalyst, to evaluate the influence of the physical properties of the ionic liquids on the polymerisation reaction carried out in the biphasic ionic liquid/hexane mode. Two alkylaluminium compounds, AlEtCl 2 and AlEt 2 Cl, were used as activators. The influence of the activator/catalyst molar ratio on the performance of the ethylene polymerisation was determined for each ionic liquid studied. The best results were obtained using 1- n -octyl-3-methylimidazolium tetrachloroaluminate. …

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryGeneral Physics and AstronomySolution polymerizationPost-metallocene catalystCatalysischemistry.chemical_compoundchemistryPolymerizationTetrachloroaluminateIonic liquidPolymer chemistryMaterials ChemistryMetalloceneAlkylEuropean Polymer Journal
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Structural variations in amphiphiles: Discoidal multivalent cations

1986

Fourteen cationic multipolar amphiphiles have been synthesized with pyridinium or trimethylammonium head groups. The hydrophobic cores are planar ring systems (benzene or triphenylene) to which two, three, four, or six decylene or undecylene alkyl chains are attached by ester linkages. The hydrophilic head groups are bound to the outer ends of the alkyl chains.

chemistry.chemical_classificationPolymers and PlasticsStereochemistryChemistryCationic polymerizationTriphenyleneRing (chemistry)Micellechemistry.chemical_compoundColloid and Surface ChemistryLiquid crystalPolymer chemistryAmphiphileMaterials Chemistrylipids (amino acids peptides and proteins)PyridiniumPhysical and Theoretical ChemistryAlkylColloid & Polymer Science
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Study on compatibilization of polypropylene-liquid crystalline polymer blends

1997

The mechanical properties, melt rheology, and morphology of binary blends comprised of two polypropylene (PP) grades and two liquid crystalline polymers (LCP) have been studied. Compatibilization with polypropylene grafted with maleic anhydride (PP-g-MAH) has been attempted. A moderate increase in the tensile moduli and no enhancements in tensile strength have been revealed. Those findings have been attributed to the morphology of the blends, which is predominantly of the disperse mode. LCP fibers responsible for mechanical reinforcement were only exceptionally evidenced. Discussion of PP-LCP interfacial characteristics with respect to mechanical properties-morphology interrelations allowed…

chemistry.chemical_classificationPolypropyleneMaterials sciencePolymers and PlasticsMaleic anhydrideGeneral ChemistryPolymerCompatibilizationSurfaces Coatings and Filmschemistry.chemical_compoundchemistryRheologyLiquid crystalUltimate tensile strengthPolymer chemistryMaterials ChemistryPolymer blendComposite materialJournal of Applied Polymer Science
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