Search results for "Molar"

showing 10 items of 1069 documents

Hygrothermal ageing of reprocessed polylactide

2012

[EN] The influence of an accelerated hygrothermal ageing simulation test on a commercial PLA and its three subsequent mechanically-reprocessed materials was studied. The analysis was focused on the water diffusion kinetics and the physico-chemical changes induced by the hygrothermal degradation. Water diffusion proceeded faster than chain relaxation processes, as defined by a Case II absorption model. It was proved that the water diffusion rate decreased with subsequent reprocessing cycles and increased with higher hygrothermal ageing temperatures. Hydrolytic chain scission provoked significant molar mass decays and consequent general losses of thermal and mechanical performance. The rearra…

Materials scienceMolar massSolucions polimèriquesPolymers and PlasticsKineticsTermoplàsticsHygrothermal ageingDifferential scanning calorimetry (DSC)Water absorption kineticsCondensed Matter PhysicsAbsorbanceCrystallinityDifferential scanning calorimetryPolylactide (PLA)Mechanics of MaterialsAgeingFourier-transform infrared analysis (FT-IR)MAQUINAS Y MOTORES TERMICOSMaterials ChemistryCrystalliteComposite materialAbsorption (electromagnetic radiation)Crystallinity
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Optical aging behaviour naturally induced on As_2S_3 microstructured optical fibres

2014

The efficiency and the stability of As2S3 microstructured optical fibres (MOFs) are limited by the shift of their optical properties that occurs over time due to a naturally induced aging process. Such sensitivity becomes more crucial for long optical path. Among the variety of fibre designs, the MOFs are developed for promising photonics applications such as supercontinuum generation for example. In the present work, we carried out an extensive aging study on As2S3 chalcogenide MOFs in ambient atmosphere. The evolution of the fibre transmission spectrum has been studied with regards to exposure time. The analysis of the transmission line profile was performed in terms of different spectral…

Materials scienceOptical fiberbusiness.industryChalcogenideAttenuationMicrostructured optical fiberMolar absorptivityElectronic Optical and Magnetic MaterialsSupercontinuumlaw.inventionchemistry.chemical_compoundOpticsOptical pathchemistrylawOptoelectronicsPhotonicsbusinessOptical Materials Express
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Über den absolutwert des fehlers bei der bestimmung von molekulargewichtsverteilungen mit der GPC-methode (messungen an polymethylmethacrylaten)

1970

Die Gelpermeationschromatographie (GPC) liefert unter konventionellen und definierten Bedingungen Molekulargewichtsverteilungen, die i. allg. um einen bestimmten Betrag zu breit sind. Um diesen Fehler quantitativ zu bestimmen, werden Fraktionen von Polymethylmethacrylat (PMMA) hergestellt, deren Uneinheitlichkeit (Mw/Mn - 1) durch osmotische und Lichtstreuungs- bzw. viskometrische Messungen bestimmt werden. Ferner werden unter definierten Bedingungen Polymerisate hergestellt, deren Uneinheitlichkeit durch die Kinetik und andere Kontrollen festgelegt ist. Unter Verwendung dieser Werte kann man Mw/Mn an PMMA auf wenige Prozent genau bestimmen und Molekulargewichtsverteilungen auf Grund korrig…

Materials sciencePolymer chemistryAnalytical chemistryMolar mass distributionDie Makromolekulare Chemie
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Synthesis of block copolymers with poly(methyl methacrylate): P(B-b-MMA), P(EB-b-MMA), P(S-b-B-b-MMA) and P(S-b-EB-b-MMA)

1993

Well-defined diblock copolymers poly(butadiene-b-methyl methacrylate) (=P(B-b-MMA)) and triblock copolymers poly(styrene-b-butadiene-b-methyl methacrylate) (=P(S-b-B-b-MMA)) have been prepared by sequential anionic polymerization in THF. The synthesis of P(B-b-MMA) and P(S-b-B-b-MMA) was most efficient in the presence of lithium alkoxides. By this method side reactions are suppressed and the polymerization can be performed at higher temperatures. The resulting triblock copolymers have narrow molecular weight distribution. The 1,2-PB midblock was quantitatively hydrogenated with tosylhydrazide to enhance thermal stability. Alternatively the hydrogenation can be performed at elevated pressure…

Materials sciencePolymers and PlasticsButanoneGeneral ChemistryCondensed Matter PhysicsMethacrylatePoly(methyl methacrylate)chemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationvisual_artAlkoxidePolymer chemistryMaterials ChemistryCopolymervisual_art.visual_art_mediumMolar mass distributionPolymer Bulletin
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Testing of a kinetics equation of mechanical degradation

1987

A modification of the kinetics equation of mechanical degradation of Harrington and Zimm is proposed to fit experimental data taken on a molten polystyrene. This equation is applied to each molecular weight of the discretized molecular weight distribution curve, and the limiting molecular weight is determined for each molecular weight. With this modification the theoretical curves fit both Mw and Mn curves well.

Materials sciencePolymers and PlasticsDiscretizationKineticsThermodynamicsGeneral ChemistryLimitingchemistry.chemical_compoundchemistryKinetic equationsKinetics equationMaterials ChemistryMolar mass distributionDegradation (geology)Physical chemistryPolystyrenePolymer Engineering and Science
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Modelling polycarbonate synthesis rates on the example of bulk heteropolyaddition of diphenyl carbonate and bisphenol A diglycidyl ether

2016

This paper investigates the effects of increased reaction mixture viscosity on the kinetics of linear polymer creation in a bulk polyaddition process of diphenyl carbonate and bisphenol A diglycidyl ether. The paper presents a method for solving a system of bulk polyaddition of diphenyl carbonate and bisphenol A diglycidyl ether process balance equations, allowing the determinatiof the process kinetic parameters. Determination of polymerisation reaction kinetic parameters was also made possible by the use of the so-called partial reaction rate constant. Such an approach enabled a significant simplification of the mathematical expressions describing the heteropolyaddition process and provide…

Materials sciencePolymers and PlasticsKineticsreaction rate constantKinetics of polymerisations02 engineering and technology010402 general chemistry01 natural sciencesViscositychemistry.chemical_compoundReaction rate constantmodelling of polymerizationsMaterials ChemistryOrganic chemistryPolycarbonateBisphenol A diglycidyl etherMolar massheteropolyadditionGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicslinear polymer0104 chemical sciencesChemical engineeringPolymerizationDiphenyl carbonatechemistryvisual_artviscosityvisual_art.visual_art_medium0210 nano-technologyPolymer Bulletin
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Material valorisation of amorphous polylactide. Influence of thermo-mechanical degradation on the morphology, segmental dynamics, thermal and mechani…

2012

[EN] This paper reports the effects of multiple mechanical recycling on the structure and properties of amorphous polylactide (PLA). The influence of the thermo-mechanical degradation induced by means of five successive injection cycles was initially addressed in terms of macroscopic mechanical properties and surface modification. A deeper inspection on the structure and morphology of PLA was associated to the thermal properties and viscoelastic behaviour. Although FT-IR analysis did not show significant changes in functional groups, a remarkable reduction in molar mass was found by viscometry. PLA remained amorphous throughout the reprocessing cycles, but the occurrence of a cold-crystalli…

Materials sciencePolymers and PlasticsMechanical propertiesViscoelasticityThermo-mechanical degradationThermodynamic propertiesDegradationSegmental dynamicsCold-crystallizationMaterials ChemistryMechanical recyclingRecyclingComposite materialMaterialsMolar massTermoplàsticsViscometerDynamic mechanical analysisCondensed Matter PhysicsMaterial valorisationAmorphous solidDynamicsPolylactide (PLA)Mechanics of MaterialsPolylactidesMAQUINAS Y MOTORES TERMICOSFunctional groupsSurface modificationRelaxation (physics)Degradation (geology)
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Direct synthesis of fibrous high molecular weight polyethylene using vanadium catalysts supported on an SiO2ionic liquid system

2015

Polyethylene of fibrous morphology was obtained using Cp2VCl2 and VCl2(salenCl2) catalysts activated by AlEt2Cl and AlEtCl2 and heterogenized on a supported ionic liquid system prepared with SiO2 and 1-(3-triethoxysilyl)propyl-3-methylimidazolium chloroaluminate. The fibre length ranges from 15 to 60 µm, depending on the reaction conditions. The polyethylene is characterized by a high molecular weight ((1.1–2.4) × 106 g mol−1) and a narrow molecular weight distribution (1.4–2.5). It is a linear polymer, properly without branching. The DSC method reveals characteristic changes in melting temperature and crystallinity degree between the first and second scan heating cycles (141 °C and 136 °C,…

Materials sciencePolymers and PlasticsOrganic ChemistryPolyethylenePost-metallocene catalystBranching (polymer chemistry)Catalysischemistry.chemical_compoundCrystallinitychemistryChemical engineeringIonic liquidPolymer chemistryMaterials ChemistryMolar mass distributionFourier transform infrared spectroscopyPolymer International
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Temperature Variation Enables the Design of Biobased Block Copolymers via One‐Step Anionic Copolymerization

2021

A one-pot approach for the preparation of diblock copolymers consisting of polystyrene and polymyrcene blocks is described via a temperature-induced block copolymer (BCP) formation strategy. A monomer mixture of styrene and myrcene is employed. The unreactive nature of myrcene in a polar solvent (tetrahydrofuran) at -78 °C enables the sole formation of active polystyrene macroinitiators, while an increase of the temperature (-38 °C to room temperature) leads to poly(styrene-block-myrcene) formation due to polymerization of myrcene. Well-defined BCPs featuring molar masses in the range of 44-117.2 kg mol-1 with dispersities, Ð, of 1.09-1.21, and polymyrcene volume fractions of 30-64% are acc…

Materials sciencePolymers and PlasticsPolymers02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationStyrenechemistry.chemical_compoundMaterials ChemistryCopolymerMolar massOrganic ChemistryTemperature021001 nanoscience & nanotechnology0104 chemical sciencesMolecular WeightMonomerAnionic addition polymerizationchemistryChemical engineeringPolymerizationPolystyrenesSelf-assemblyPolystyrene0210 nano-technologyMacromolecular Rapid Communications
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Dielectric Spectroscopy of Recycled Polylactide

2014

The effects of multiple mechanical recycling on amorphous polylactide (PLA) were simulated by means of five successive injection-grinding cycles. The influence of the induced thermo-mechanical degradation on the dielectric properties of PLA was analysed. The relaxation spectra were studied in terms of the complex dielectric permittivity (ε0 and ε00) and the dielectric loss tangent, tg(d) in the frequency range from 102 to 107 Hz over the temperature interval from 0 C to 140 C. It was possible to distinguish two relaxations zones, one at low temperatures and high frequencies (b relaxation) and another at higher temperatures and lower frequencies (a relaxation). The individual relaxations wer…

Materials sciencePolymers and PlasticsThermodynamicsDielectricConductivityThermo-mechanical degradationsymbols.namesakeSegmental dynamicsDynamic fragilityMaterials ChemistryPoly(lactide) (PLA)RecyclingComposite materialResistència de materialsArrhenius equationMolar massCondensed Matter PhysicsDielectric spectroscopyAmorphous solidMechanics of MaterialsMAQUINAS Y MOTORES TERMICOSsymbolsRelaxation (physics)Dielectric lossMATEMATICA APLICADADielectric thermal analysis (DETA)
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