Search results for "Copolyester"

showing 10 items of 18 documents

Effect of Graphene Nanoplatelets on the Physical and Antimicrobial Properties of Biopolymer-Based Nanocomposites

2016

In this work, biopolymer-based nanocomposites with antimicrobial properties were prepared via melt-compounding. In particular, graphene nanoplatelets (GnPs) as fillers and an antibiotic, i.e., ciprofloxacin (CFX), as biocide were incorporated in a commercial biodegradable polymer blend of poly(lactic acid) (PLA) and a copolyester (BioFlex®). The prepared materials were characterized by scanning electron microscopy (SEM), and rheological and mechanical measurements. Moreover, the effect of GnPs on the antimicrobial properties and release kinetics of CFX was evaluated. The results indicated that the incorporation of GnPs increased the stiffness of the biopolymeric matrix and allowed for the t…

BiocideMaterials scienceScanning electron microscopeKineticsAntimicrobial activity; Ciprofloxacin; Drug release; Graphene nanoplatelets (GnPs); Nanocomposites; Poly(lactic acid) (PLA); Materials Science (all)02 engineering and technologyengineering.material010402 general chemistry01 natural scienceslcsh:TechnologyArticlepoly(lactic acid) (PLA)ciprofloxacinnanocompositesGeneral Materials ScienceComposite materiallcsh:Microscopydrug releaselcsh:QC120-168.85NanocompositeNanocompositeantimicrobial activitylcsh:QH201-278.5lcsh:T021001 nanoscience & nanotechnologyAntimicrobialBiodegradable polymerCopolyestergraphene nanoplatelets (GnPs)0104 chemical sciencesChemical engineeringnanocomposites; graphene nanoplatelets (GnPs); poly(lactic acid) (PLA); antimicrobial activity; drug release; ciprofloxacinlcsh:TA1-2040engineeringlcsh:Descriptive and experimental mechanicsMaterials Science (all)Biopolymerlcsh:Electrical engineering. Electronics. Nuclear engineering0210 nano-technologylcsh:Engineering (General). Civil engineering (General)lcsh:TK1-9971Materials; Volume 9; Issue 5; Pages: 351
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On the use of PET-LCP copolymers as compatibilizers for PET/LCP blends

1996

Copolyesters of poly[ethylene terephthalate) (PET) with a liquid crystalline polymer (LCP), SBH 1:1:2, have been synthesized by the polycondensation, carried out in the melt at temperatures up to 300 degrees C of sebacic acid (S), 4,4'-dihydroxybiphenyl (B), and 4-hydroxybenzoic acid (H) in the presence of PET. The PET-SBH copolyesters have been characterized by differential scanning calorimetry, scanning electron microscopy, X-ray diffraction, etc., and the relationships between properties and preparation conditions are discussed. The copolyesters show a biphasic nature, which is more evident for the products synthesized with a thermal profile comprising relatively lower temperatures (220-…

Condensation polymerMaterials sciencePolymers and PlasticsSebacic acidPOLY(ETHYLENE-TEREPHTHALATE)POLYPHENYLENE SULFIDEchemistry.chemical_compoundDifferential scanning calorimetryPOLYETHYLENE TEREPHTHALATETHERMOTROPIC POLYESTERUltimate tensile strengthPolymer chemistryMaterials ChemistryCopolymerchemistry.chemical_classificationMECHANICAL-PROPERTIESGeneral ChemistryPolymerCopolyesterLIQUID-CRYSTALLINE POLYMERSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiMonomerchemistryChemical engineeringCOPOLYESTERFLEXIBLE SPACERMORPHOLOGYFIBERS
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Properties of radiation-modified blends of polyethylene with elastomers and liquid crystalline copolyester

2001

The results are given on the effect of γ-irradiation on properties of blends of high and low-density polyethylene (HDPE, LDPE) with elastomers -ethylene/propylene/diene rubber (EPDM) and chlorinated polyethylene (CPE), and thermotropic liquid crystalline polymer (LCP). The morphological, thermal, mechanical properties (including thermosetting properties) and adhesion properties of blended composites were investigated. A special attention was paid to the applicability of the blends as thermosetting materials (TSM). The LCP used was a copolyester of poly(ethylene terephthalate) with p-(hydroxybenzoic acid) in the ratio 40: 60. It was found that addition of LCP essentially influenced the therm…

Hydroxybenzoic acidMaterials sciencePolymers and PlasticsEPDM rubberOrganic ChemistryThermosetting polymerPolyethyleneCondensed Matter PhysicsCopolyesterchemistry.chemical_compoundLow-density polyethylenechemistryMaterials ChemistryPolymer blendHigh-density polyethyleneComposite materialMacromolecular Symposia
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Miscibility and properties of linear poly(l-lactide)/branched poly(l-lactide) copolyester blends

2006

Abstract Polymer blends consisting of linear poly( l -lactide) (PLLA) and different proportions of dendritic PLLA-based copolyesters ( hb -PLLA) characterized by different degrees of branching (DB) were obtained in melt. The solid-state properties of poly( l -lactide)s and their blends were investigated by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), atomic force microscopy (AFM) and stress–strain measurements. DSC and DMA methods proved miscibility of PLLA/ hb -PLLA blends for the studied composition range. AFM indicated that no phase separation occurs in PLLA/ hb -PLLA blends and that PLLA and hb -PLLA cocrystallize in one single lamellae type. The mechanica…

LactideMaterials sciencePolymers and PlasticseducationOrganic Chemistrytechnology industry and agricultureDynamic mechanical analysisBiodegradationBranching (polymer chemistry)MiscibilityCopolyesterchemistry.chemical_compoundDifferential scanning calorimetryChemical engineeringchemistryPolymer chemistryMaterials ChemistryPolymer blendPolymer
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Static and dynamic elasticity of some thermotropic liquid-crystalline copolyesters

1997

Two series of thermotropic liquid crystalline copolyesters were studied in static and dynamic tensile deformation. Static loading generally does not lead to any peculiar phenomena: the stress-strain diagrams are linear or convex, except one copolyester fibre, the stress-strain diagram of which is concave at high temperatures. On the contrary, in dynamic loading the elasticity modulus increased during deformation for all the samples investigated. So it can be assumed that formation of a more rigid and stable structure takes place due to the dynamic deformation.

Materials sciencePolymers and PlasticsGeneral MathematicsCondensed Matter PhysicsCopolyesterThermotropic crystalBiomaterialsSynthetic fiberMechanics of MaterialsDynamic loadingSolid mechanicsUltimate tensile strengthCeramics and CompositesComposite materialDeformation (engineering)Elastic modulusMechanics of Composite Materials
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Thermomechanical properties of radiation-modified blends of polyethylene with liquid crystalline copolyester

1999

The results of investigation of gamma irradiated blends of high-density polyethylene (PE) with thermotropic polymer liquid crystal (PLC) are presented. The PLC used was a copolyester of 40% poly(ethylene terephthalate) with 60% p-(hydroxy-benzoic acid). The PLC content in the blends was 0, 5, and 10 wt%. The constituents were blended with the use of a single screw extruder. The specimens were prepared by compression molding. The irradiation of the samples was performed by a Co 60 γ-radiation source in inert atmosphere (argon) up to absorbed relatively low doses (up to 200 kGy: 1 Mrad = 10 kGy). The morphological, thermal, and mechanical properties were investigated for irradiated and unirra…

Materials sciencePolymers and PlasticsThermosetting polymerCompression moldingGeneral ChemistryPolyethyleneThermotropic crystalCopolyesterchemistry.chemical_compoundchemistryMaterials ChemistryMelting pointIrradiationPolymer blendComposite materialPolymer Engineering & Science
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Reactive blending of a functionalized polyethylene with a semiflexible liquid crystalline copolyester

1996

Reactive blends (50/50 w/w) of a low molar mass polyethylene containing free carboxylic groups (PEox) and a semiflexible liquid crystalline polyester (SBH 1 : 1 : 2, by Eniricerche) have been prepared at 240 degrees C in a Brabender mixer, in the presence of Ti(OBu)(4) catalyst, for different mixing times (15, 60, and 120 min). In order to prove the formation of a PE-g-SBH copolymer, the blends have been fractionated by successive extractions with boiling toluene and xylene. The soluble fractions and the residues have been analyzed by Fourier transform infrared (FTIR) spectroscopy, thermogravimetry (TG and DTG), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM)…

Molar massPolymers and PlasticsCOMPATIBILIZATIONChemistryGeneral ChemistryPolyethyleneCopolyesterTHERMOPLASTIC COMPOSITESSurfaces Coatings and FilmsPolyesterThermogravimetrychemistry.chemical_compoundDifferential scanning calorimetryPOLYMER BLENDSSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiChemical engineeringPolymer chemistryTRANSESTERIFICATIONMaterials ChemistryMORPHOLOGYThermal stabilityFourier transform infrared spectroscopyPOLYPROPYLENEPOLYESTERS
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Strukturuntersuchung von polyestern durch direkten abbau im massenspektrometer, 4. Polyester und copolyester der milchsäure und glykolsäure

1978

Polyesters and copolyesters of 2-hydroxyacetic acid (glycolic acid) and 2-hydroxypropionic acid (lactic acid) were investigated by direct pyrolysis in the ion source of a mass spectrometer. Thermal degradation of these polyesters and copolyesters at 10−6 mbar yields cyclic oligomers which are further degraded by an electron impact induced mechanism by elimination of formaldehyde or acetaldehyde and CO2 to give characteristic series of linear ions. In the pyrolysis mass spectrum of a copolyester (mole ratio of monomeric units ≈1:1) intact sequences up to 8 monomeric units can be observed.

Polyesterchemistry.chemical_compoundMonomerchemistryPolymer chemistryMass spectrumFormaldehydeMass spectrometryCopolyesterGlycolic acidLactic acidDie Makromolekulare Chemie
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Inimer-Promoted Synthesis of Branched and Hyperbranched Polylactide Copolymers

2009

A series of (hyper)branched poly(l-lactide)(PLLA) copolymers has been prepared by ring-opening multibranching copolymerization of l-lactide with a hydroxyl-functional (ABB′) lactone inimer, 5HDON (5-hydroxymethyl-1,4-dioxane-2-on). Polymerization was conducted in bulk and solution and catalyzed either by stanneous-2-ethyl hexanoate (Sn(Oct)2) or an organic base, 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD). Precise structural characterization of the resulting branched copolyester structures was accomplished by a combination of 2D NMR techniques, relying on the comparison with model compounds. The 5HDON inimer was employed in 1% to 20% fractions and is incorporated either as a dendritic unit or…

Polymers and PlasticsOrganic baseChemistryOrganic ChemistryNuclear magnetic resonance spectroscopyBranching (polymer chemistry)Ring-opening polymerizationCopolyesterInorganic ChemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryTwo-dimensional nuclear magnetic resonance spectroscopyMacromolecules
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Effect of the Components Molar Mass and of the Mixing Conditions on the Compatibilization of PE/LCP Blends by PE-g-LCP Copolymers

1999

The rheology, morphology, and mechanical properties of blends of high-density polyethylene (HDPE) with a semiflexible liquid crystalline copolyester (SBH) were studied in order to assess the compatibilizing ability of added PE-g-SBH copolymers, and its dependence on the molar mass of the PE matrix, and on the technique used for blend preparation. The PE-g-SBH copolymers were synthesized as described in previous articles, either by the polycondensation of the SBH monomers in the presence of a functionalized PE sample containing free carboxyl groups, or by reactive blending of the latter polymer with preformed SBH. Two samples of HDPE having different molar masses, and two samples of SBH with…

chemistry.chemical_classificationMaterials scienceMolar massCondensation polymerPolymers and PlasticscompatibilizationGeneral ChemistryPolymerCompatibilizationPolyethyleneCopolyesterSurfaces Coatings and Filmschemistry.chemical_compoundchemistrypolyethylene-LCP blendmorphologyMaterials ChemistryCopolymerrheologyHigh-density polyethyleneComposite material
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