Search results for "Glass"

showing 10 items of 1153 documents

Long-term ISO 23936-2 sweet oil ageing of HNBR

2021

Abstract A hydrogenated nitrile butadiene rubber (HNBR) compound is subjected to ageing in a simulated oil and gas environment in accordance with ISO 23936-2 standard at two elevated temperatures (130 °C and 150 °C) for a period of up to 9 months. Shore D hardness, thermal expansion, dynamic mechanical analysis (DMA), Fourier transform infrared (FTIR) spectroscopy, compression and compression set (CS) measurements are made before and after the chemical exposure. The hardness, modulus at short times, degree of relaxation and CS increases while the coefficient of thermal expansion in HNBR tends to decrease with ageing time and temperature. Temperature is shown to impose a greater effect on th…

Materials sciencePolymers and PlasticsISO 23936-2Organic Chemistry:Plast- og komposittmaterialer: 523 [VDP]Compression setViscoelasticityContext (language use)Material degradationDynamic mechanical analysisHNBRThermal expansion:Polymer and plastics: 523 [VDP]TP1080-1185ddc:540Stress relaxationShore durometerPolymers and polymer manufactureComposite materialGlass transitionSweet oil ageingElastic modulus
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Dynamic mechanical properties of semi-interpenetrating networks based on poly(styrene-co-maleic anhydride): 3. Poly(2,6-dimethyl-1,4-phenylene ether)…

1994

Semi-IPN's based on linear poly(2,6-dimethyl-1,4-phenylene ether) (PPE) and diamine crosslinked poly(styrene-co-maleic anhydride) (PScoMA) copolymers containing small amounts of maleic anhydride (PSA=4.7wt.-% MA, PSB=5.8 wt-% MA) are studied with respect to the influence of cross-linking on the phase behavior. Temperature-dependent dynamic mechanical analysis (DMA) and DSC show that the semi-IPN's prepared from concentrated solution show weak crystallinity of the PPE phase. After heating above the PPE melting transition the semi-IPN's remain amorphous and the relaxation in the glass transition region as well as the terminal relaxation of the free PPE chains in the network is studied as a fu…

Materials sciencePolymers and PlasticsMaleic anhydrideDynamic mechanical analysisStyrenechemistry.chemical_compoundCrystallinityColloid and Surface ChemistrychemistryPhenyleneDiaminePolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistryGlass transitionColloid and Polymer Science
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Mechanical properties of pultruded glass fiber reinforced plastic after freeze–thaw cycling

2012

The use of pultruded fiber-reinforced plastics in civil infrastructure requires the long-term prediction of their mechanical properties, which should be based on understanding and estimating the processes in the structure under action of aggressive environmental factors: humidity and freeze–thaw cycles. This article reports on results of short-term exposure to severe freeze–thaw cycling in the temperature range from –30°C to 20°C of polyester-based glass fiber reinforced plastic both dry and wet. The effect of freeze–thaw cycling of flat specimens cut from I-beam pultruded profile was estimated by use of three-point-bending tests and dilatometric investigation in the temperature range from…

Materials sciencePolymers and PlasticsMechanics of MaterialsPultrusionMechanical EngineeringGlass fiberMaterials ChemistryCeramics and CompositesComposite materialFibre-reinforced plasticCivil infrastructureFreeze thaw cyclingJournal of Reinforced Plastics and Composites
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Poly(styrene-b-methyl methacrylate) block copolymers as compatibilizing agents in blends of poly(styrene-co-acrylonitrile) and poly(2,6-dimethyl-1,4-…

1993

Abstract The compatibilizing effect of the symmetric narrowly distributed block copolymer poly(styrene- b -methyl methacrylate) (P(S- b -MMA)) in blends of high-molecular-weight poly(styrene- co -acrylonitrile) containing 20 wt% (PSAN20) or 43 wt% acrylonitrile (PSAN43) with poly(2,6-dimethyl-1,4-phenylene ether) (PPE) was investigated by dynamic mechanical spectroscopy and transmission electron microscopy. In blends with the PSAN43, P(S- b -MMA) forms spherical micelles in the PPE phase with no dispersing efficiency. In contrast to this, for blends with PSAN20, the block copolymer is located at the phase boundary, causing an extremely fine dispersion of the components. Depending on the loc…

Materials sciencePolymers and PlasticsOrganic ChemistryCompatibilizationMicelleStyrenechemistry.chemical_compoundchemistryPhenylenePolymer chemistryMaterials ChemistryCopolymerMethyl methacrylateAcrylonitrileGlass transitionPolymer
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Thermal behavior and spherulitic superstructures of SBC triblock copolymers based on polystyrene (S), polybutadiene (B) and a crystallizable poly(ɛ-c…

1996

The dynamic crystallization and the melting behavior of polystyrene-block-poly(e-caprolactone) (PS-b-PCL, short notation SC), polybutadiene-block-poly(e-caprolactone) (PB-b-PCL, BC) and polystyrene-block-polybutadiene-block-poly(e-caprolactone) (PS-b-PB-b-PCL, SBC) have been studied using differential scanning calorimetry. The copolymers with high molecular weight exhibit microphase separation into microphases consisting of polystyrene, polybutadiene and poly(e-caprolactone) and partial crystallization of the corresponding PCL block. The crystallization occurs at temperatures below the PS glass transition. Depending on the block copolymer composition, crystallization takes place through a c…

Materials sciencePolymers and PlasticsOrganic ChemistryCondensed Matter Physicslaw.inventionAvrami equationchemistry.chemical_compoundPolybutadieneDifferential scanning calorimetrychemistrylawPolymer chemistryMaterials ChemistryMelting pointCopolymerPolystyrenePhysical and Theoretical ChemistryCrystallizationGlass transitionMacromolecular Chemistry and Physics
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Poly(styrene-b-methyl methacrylate) block copolymers as compatibilizing agents in blends of poly(styrene-co-acrylonitrile) and poly(2,6-dimethyl-1,4-…

1993

Abstract The influence of the molecular weight of the symmetric block copolymer poly(styrene-b-methyl methacrylate) (P(S-b-MMA)) in blends with high-molecular-weight poly(styrene-co-acrylonitrile) (PSAN) and poly(2,6-dimethyl-1,4-phenylene ether) (PPE) is investigated by dynamic mechanical analysis and transmission electron microscopy. Total molecular weights of the block copolymers vary from 16 up to 275 kg mol−1. Independent of molecular weight, all block copolymers locate to the interface with strong dispersing efficiency. The different block copolymers also showed approximately the same emulsifying efficiency. The degree of segmental mixing of the blocks with the respective phases is ev…

Materials sciencePolymers and PlasticsOrganic ChemistryDynamic mechanical analysisStyrenechemistry.chemical_compoundchemistryPhenylenePolymer chemistryMaterials ChemistryCopolymerPolystyreneAcrylonitrileMethyl methacrylateGlass transitionPolymer
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The glass transition of mixtures of polystyrene with alkyl-terminated oligostyrene — experimental evidence for microphase separation in a polymer ble…

1995

Mixtures of high molecular weight polystyrene (P n = 961.5 ; T g = 373 K) and sec-butyl-terminated oligostyrene (P n = 10.6 ; T g = 302 K) show a dependence of the glass transition on the composition (i.e., number-average molecular weight) which cannot be described by the classic equations of Fox & Flory or Kanig & Ueberreiter. Addition of small amounts of the oligostyrene strongly decreases the glass transition, and above an oligomer content of 40 wt.-% the glass transition remains constant within experimental error. This behavior can be attributed to the unfavorable interactions between the alkyl-terminated oligomer and the high molecular weight PS. As a result the oligomer is a bad solve…

Materials sciencePolymers and PlasticsOrganic ChemistryMaleic anhydrideCondensed Matter PhysicsOligomerStyrenechemistry.chemical_compoundEnd-groupchemistryPolymer chemistryMaterials ChemistryCopolymerPolystyrenePolymer blendPhysical and Theoretical ChemistryGlass transitionMacromolecular Chemistry and Physics
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Monte Carlo modelling of the polymer glass transition

1993

We are proposing a lattice model with chemical input for the computer modelling of the polymer glass transition. The chemical input information is obtained by a coarse graining procedure applied to a microscopic model with full chemical detail. We use this information on Bisphenol-A-Polycarbonate to predict it's Vogel-Fulcher temperature out of a dynamic Monte Carlo Simulation. The microscopic structure of the lattice model is that of a genuine amorphous material, and the structural relaxation obeys the time temperature superposition.

Materials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodCondensed Matter PhysicsCondensed Matter::Disordered Systems and Neural NetworksAmorphous solidTime–temperature superpositionMaterials ChemistryDynamic Monte Carlo methodRelaxation (physics)GranularityStatistical physicsGlass transitionLattice model (physics)Makromolekulare Chemie. Macromolecular Symposia
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Chain conformation and structure in amorphous polymers as revealed by X-ray, neutron, light and electron diffraction

1976

Abstract The physical structure of the melt, the supercooled melt, and the glassy state of amorphous polymers can be characterized by the chain conformation, the local order, and the morphology. The conformation was studied by small-angle neutron scattering. The local order was characterized by pair distribution functions which were derived from electron scattering curves. In addition, model calculations were used to gain information about short-range order. The morphology was studied by means of light scattering (density and anisotropy fluctuations), small-angle X-ray scattering (density fluctuations), and magnetic birefringence measurements (orientational order). Experiments were performe…

Materials sciencePolymers and PlasticsScatteringGeneral ChemistryNeutron scatteringCondensed Matter PhysicsSmall-angle neutron scatteringMolecular physicsLight scatteringAmorphous solidCondensed Matter::Soft Condensed MatterCrystallographyMaterials ChemistryBiological small-angle scatteringGlass transitionWide-angle X-ray scatteringJournal of Macromolecular Science, Part B
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Role of thermal history on quiescent cold crystallization of PET

2002

8 pags., 9 figs.

Materials sciencePolymers and PlasticsScatteringPET. Cold crystallization. Isothermal. Thermal history. GlassOrganic ChemistryKineticsNucleationThermodynamicsKinetic energyCondensed Matter::Disordered Systems and Neural NetworksIndentation hardnessIsothermal processlaw.inventionAmorphous solidlawPolymer chemistryMaterials ChemistryCrystallization
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