Search results for "melting"

showing 10 items of 238 documents

Synthesis and Characterization of a New Fully Aromatic LCP

1996

Abstract Liquid crystal polymers (LCP)are a relatively new class of polymers with very interesting and unusual properties. In particular, easy processability and outstanding mechanical and barrier properties make them very attractive. Unfortunately the high stiffness of their chains often leads to compounds having very high melting points and consequently to unprocessable materials. By adding a flexible segments in the chain backbone the LCPs become processable at lower temperatures but lower properties are displayed. A new rigid liquid crystalline polymer, having excellent physical properties, good processing temperature and a good cost/performance compromise, is described in this work. Th…

chemistry.chemical_classificationLIQUID-CRYSTALLINE POLYMERSMaterials sciencePolymer scienceLiquid crystallineHigh stiffnessPolymerCondensed Matter PhysicsBLENDSCharacterization (materials science)Condensed Matter::Soft Condensed MatterSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryLiquid crystalPolymer chemistryMelting pointMolecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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Reprocessing of Poly(Vinyl Chloride), Polycarbonate and Polyethyleneterephthalate

1998

Poly ethyleneterephthalate — PET- and Poly(vinyl chloride) — PVC — are two of the most frequently encountered polymers in post-consumer plastics. In particular, these polymers can be used for manufacturing the same products (bottles, for example) and therefore are often found in the same stream, even when the collection is done with separation. The recycling of PET and PVC is usually carried out by separating them and reprocessing the two homogeneous polymers. Indeed, the heterogeneous recycling of two polymers is at present almost impossible because of many problems: as their melting points are very different, at the processing temperature of PET severe degradation phenomena of PVC take pl…

chemistry.chemical_classificationMaterials scienceIzod impact strength testHydrochloric acidPolymerVinyl chloridechemistry.chemical_compoundHydrolysischemistryChemical engineeringvisual_artMelting pointvisual_art.visual_art_mediumDegradation (geology)Polycarbonate
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Polymerization of mono- and multilayer forming diacetylenes

1977

Heptadeca-2,4-diine-1-ol and Heptadeca-2,4-diine-1-acid were synthesized and their polymerization behaviour in the solid state was investigated. Both compounds polymerize thermally below the melting point and photochemically under the action of uv-light to form polymers via 1,4-addition to the conjugated triple bonds with a backbone of conjugated double-and triple-bonds. The photoresponse spectra resemble the absorption spectra exhibiting maxima of photoreactivity in the absorption band of the conjugated triple bonds of the monomers.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsAbsorption spectroscopyPolymerConjugated systemPhotochemistryTriple bondchemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryPolymerizationAbsorption bandMaterials ChemistryMelting pointPhysical and Theoretical ChemistryColloid and Polymer Science
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Influence of processing conditions on some properties of anionically synthesized polycaprolactam in presence of lithium chloride

1980

Nylon 6–LiCl systems of various concentrations were prepared by anionic polymerization of caprolactam in the presence of salt. A depression of both crystallization rate and melting temperature was evidenced through x-ray, density, and DSC analyses. Such a preliminary characterization allowed for choosing the proper conditions in order to obtain amorphous fibers from a spinning operation which was performed at a temperature lower than the pure polymer melting point. These results are of technological relevance, especially in view of obtaining, as in similar cases, large amorphous orientations through a spinning–drawing process and high-modulus fibers after subsequent crystallization. Also, t…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsCaprolactamGeneral ChemistryPolymerSurfaces Coatings and Filmslaw.inventionAmorphous solidchemistry.chemical_compoundCrystallinityAnionic addition polymerizationchemistryChemical engineeringlawPolymer chemistryMaterials ChemistryMelting pointLithium chlorideCrystallizationJournal of Applied Polymer Science
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Rheological characterization of polycaprolactam anionically synthesized in the presence of lithium chloride

1980

Melt viscosity and dynamic-mechanical data are reported for samples obtained by anionic polymerization of caprolactam, in the presence of LiCl. The full body of results is essentially in line with those previously reported relative to mixtures of inorganic salts and commercial nylon 6, In particular a drastic-decrease of the melting point and of the rate of crystallization is confirmed as well as an increase of the glass transition temperature and of the melt viscosity. Some quantitative differences exist, which may be attributed to the different molecular weight distribution in the polymers employed in the present work.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsCaprolactamGeneral ChemistryPolymerlaw.inventionchemistry.chemical_compoundNylon 6chemistryChemical engineeringlawPolymer chemistryMaterials ChemistryMelting pointLithium chlorideMolar mass distributionCrystallizationGlass transitionPolymer Engineering and Science
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Melt spinning and mechanical properties of semirigid liquid-crystal copolyesters

1993

Melt-spinning and mechanical properties of fibers of a new class of semirigid thermotropic liquid-crystal polymers are presented. These copolyesters are synthesized from 4-4′-dihydroxybiphenyl (B), 4-hydroxybenzoic acid (H), and flexible units provided by aliphatic diacids. The flexible units depress the melting temperature without strongly depressing the mechanical properties. These liquid-crystal polymers can be easily spun at high draw ratios. Indeed, unlike rigid liquid-crystal polymers, relatively high draw ratios are needed to attain high mechanical strength. Tensile moduli of about 28 GPa and tensile strengths of about 350 MPa are obtained. © 1993 John Wiley & Sons, Inc.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsMelting temperaturePolymerCondensed Matter PhysicsThermotropic crystalchemistryLiquid crystalUltimate tensile strengthMechanical strengthMaterials ChemistryPhysical and Theoretical ChemistryComposite materialMelt spinningJournal of Polymer Science Part B: Polymer Physics
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Crystallization kinetics of LDPE/Ny6 blends

1988

The crystallization behaviour of low density polyethylene/nylon 6 blends has been investigated as a function of the composition. The melting points of the polymers are almost uninfluenced by the presence of the other homopolymers except for blends with a nylon content of 75–90%. Blends with 10% nylon content do not exhibit the crystallization peak during the cooling step probably because of the low concentration and high viscosity of the low density polyethylene matrix. The crystallinity degree of the polyethylene is independent of the composition, while some variations are shown by the polyamide. Finally the rate of nucleation is strongly affected by the composition, in particular for the …

chemistry.chemical_classificationMaterials sciencetechnology industry and agricultureNucleationPolymerPolyethylenelaw.inventionLow-density polyethylenechemistry.chemical_compoundCrystallinityNylon 6chemistryChemical engineeringlawPolymer chemistryMelting pointCrystallizationJournal of thermal analysis
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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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Thermomechanical Properties of Radiation-Modified Polyethylene/Ethylene-Propylene-Diene Copolymer/Liquid-Crystalline Copolyester Blends

1999

Radiation-modified blends of high-density polyethylene (PE) with ethylene-propylene-diene copolymer (EPDM; 10-65 wt.%) and thermotropic liquid-crystalline polymer (LCP; 10 wt.%) were investigated. The LCP was a liquid-crystalline copolyester of 40% poly(ethylene terephthalate) with 60% 4-hydroxybenzoic acid. The constituents were blended using a circular extruder, the specimens were prepared by compression molding and irradiated by 60Co γ-radiation up to 200 kGy. Mechanical, thermal, and morphological properties in wide temperature range were investigated for the irradiated and non-irradiated specimens. The effects of irradiation on the thermomechanical behaviour of the PE matrix are discus…

chemistry.chemical_classificationThermosetting polymerCompression moldingGeneral ChemistryPolymerEthylene propylene rubberPolyethyleneCopolyesterThermotropic crystalchemistry.chemical_compoundchemistryPolymer chemistryMelting pointComposite materialCollection of Czechoslovak Chemical Communications
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1,2,4-Triazoles. Improved synthesis of 5-substituted 4-amino-3-mer-cato-(4H)-1,2,4-triazoles and a facile route to 3,6-disubstituted 1,2,4-triazolo[3…

1997

The reaction of thiocarbohydrazide with carboxylic acids at the melting temperature allows an improved preparation of the S-substituted 4-amino-3-mercapto-1,2,4-triazole heterocycles. The crude 4-amino-5-mercapto-1,2,4-triazoles react easily with carboxylic acids or carboxylic acid chlorides to afford the 1,2,4-triazolo[3,4-fc][1,3,4]thiadiazole ring system.

chemistry.chemical_classificationThiocarbohydrazidechemistry.chemical_compoundThiadiazoleschemistryMelting temperatureCarboxylic acidOrganic ChemistryRing (chemistry)Medicinal chemistryJournal of Heterocyclic Chemistry
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