Search results for "Plastics"

showing 10 items of 2724 documents

Well-defined carbohydrate-based polymers in calcium carbonate crystallization: Influence of stereochemistry in the polymer side chain on polymorphism…

2015

Abstract In this work we demonstrate the remarkable phase control on the crystallization of calcium carbonate by the stereochemistry of carbohydrate-based polymers. The polymers (poly(2-(2,3,4,6-tetra-O-acetyl-β- d -glucosyloxy)ethyl methacrylate) and poly(2-(2,3,4,6-tetra-O-acetyl-β- d -galactosyloxy)ethyl methacrylate)) have been synthesized from the respective glucose or galactose containing monomers (3 step synthesis) by RAFT polymerization leading to well-defined carbohydrate-based polymers with number averages of the molecular weights (Mw) of 10,000–18,000 g/mol and a dispersities (Đ) from 1.1 to 1.2. For the deprotected polymers we found differences in the phase selection of calcium …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsStereochemistryOrganic ChemistryGeneral Physics and AstronomyPolymerMethacrylatelaw.inventionchemistry.chemical_compoundCalcium carbonateMonomerchemistryPolymorphism (materials science)lawPolymer chemistryMaterials ChemistrySide chainOrganic chemistryReversible addition−fragmentation chain-transfer polymerizationCrystallizationEuropean Polymer Journal
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Master curves of viscoelastic behavior in the plastic region of a solid polymer

1977

Stress relaxation and creep tests following strain ramps were made on Mylar, both above and below the yield stress. The ramp velocity was varied over a 40-fold range. All data exhibit nonlinear viscoelastic behavior. However, those obtained above the yield point, i.e., in the plastic region, could be reduced to single master curves for both the creep and the relaxation tests by means of a simple time shift factor. This factor is inversely proportional to the strain rate existing just prior to the test.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsStrain (chemistry)General ChemistryPolymerStrain rateViscoelasticitySurfaces Coatings and FilmsNonlinear systemchemistryCreepMaterials ChemistryStress relaxationForensic engineeringRelaxation (physics)Composite materialJournal of Applied Polymer Science
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Block and graft copolymers of 2-oxazolines

1994

The cationic ring-opening polymerization of 2-oxazolines is known to be initiated by alkyl halides, Lewis acids and esters of strong acids. The polymerization proceeds by a living mechanism. Numerous block and graft copolymers have already been described. Recently it was found that chloroformates (R-O-CO-CI) are also useful initiators. The mechanism of the initiation and propagation is discussed. This type of initiators allows the synthesis of different novel two-block and three-block copolymers, star-shape polymers, and a graft copolymer with a polyvinylacetate backbone.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsStrong acidsOrganic ChemistryCationic polymerizationPolymerCondensed Matter PhysicsBlock (periodic table)chemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerLewis acids and basesAlkylMacromolecular Symposia
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Rheological behavior and thermal stability of poly(phenylene sulfide)/vectra-B950 blends

1994

Blends of polyphenylene sulfide (PPS) with a commercial, wholly aromatic, liquid crystalline polymer (LCP), Vectra-B950, have been prepared by melt-blending. Their rheological behavior has been studied in order to determine if the LCP displays a processing aid ability, and under what conditions it gives rise to potentially reinforcing fibrils dispersed in the PPS matrix. The problem of the thermal stability of PPS/LCP blends, which has been considered by some authors as the main obstacle to the production of usable materials due to the evolution of gaseous substances during processing, has been discussed. © 1994 John Wiley & Sons, Inc.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSulfideGeneral ChemistryPolymerSurfaces Coatings and FilmsViscositychemistryChemical engineeringRheologyLiquid crystalPhenylenePolymer chemistryMaterials ChemistryThermal stabilityProcessing aidJournal of Applied Polymer Science
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Dynamics of supramolecular associative polymer networks at the interplay of chain entanglement, transient chain association, and chain‐sticker cluste…

2019

The dynamic mechanical properties of supramolecular associative polymer networks depend on the average number of entanglements along the network‐forming chains, Nₑ, and on their content of associative groups, f. In addition, there may be further influence by aggregation of the associative groups into clusters, which, in turn, is influenced by the chemical structure of these groups, and again by Nₑ and f of the polymer. Therefore, the effects of these parameters are interdependent. To conceptually understand this interdependency, we study model networks in which (a) Nₑ, (b) f, and (c) the chemical structure of the associative groups are varied systematically. Each network is probed by rheolo…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSupramolecular chemistry02 engineering and technologyQuantum entanglementPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesTurn (biochemistry)Chain (algebraic topology)chemistryChemical physicsMaterials ChemistryCluster (physics)Physical and Theoretical Chemistry0210 nano-technologyCluster analysisAssociative propertyJournal of Polymer Science Part B: Polymer Physics
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Modeling the nonlinear deformation of flax-fiber-reinforced polymer matrix laminates in active loading

2015

In an attempt to fully utilize the mechanical properties of bast fibers in polymer-matrix composites, unidirectional (UD) or quasi-UD flax-fiber-reinforced composites are being developed and characterized. Their response in tension is markedly nonlinear both in on- and off-axis loading. A semiempirical tensor-linear model is applied to describe such deformation nonlinearity in active combined loading. The deformation model of UD ply, combined with an elementary laminate theory, is used to predict the stress–strain curves of laminated composites in tension. Reasonable accuracy of prediction is demonstrated for fiber-dominated layups.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsTension (physics)Mechanical EngineeringPolymerDeformation (meteorology)Flax fiberNonlinear systemMatrix (mathematics)chemistryMechanics of MaterialsMaterials ChemistryCeramics and CompositesBast fibreComposite materialTensile testingJournal of Reinforced Plastics and Composites
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Effects of filler type and mixing method on the physical properties of a reinforced semirigid liquid crystal polymer

1996

Semirigid liquid crystalline polymers (LCPs) show some advantages with respect to rigid LCP: in particular lower processing temperatures, better compatibility with flexible thermoplastics, but also some disadvantages. Thermal resistance of rigid LCPs is much better and the maximum working temperature is, in general, very high. The thermomechanical properties can be improved by adding inorganic fillers. In this work processing, mechanical and thermomechanical properties of a filled semirigid liquid crystal copolyester are reported. Several inorganic fillers have been used in order to put in evidence the influence of shape and dimensions of the particles on the properties of the filled materi…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsThermal resistanceOrganic ChemistryGlass fiberGeneral Physics and AstronomyMECHANICAL-PROPERTIESPolymerBLENDSCopolyesterSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiTHERMOTROPIC POLYESTERINJECTION MOLDINGSchemistryCreepLiquid crystalUltimate tensile strengthMaterials ChemistryFLEXIBLE SPACERComposite materialElastic modulusEuropean Polymer Journal
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Influence of the cross-linking density on the main dielectric relaxation of poly(methyl acrylate) networks.

2005

A series of polymer networks of varying cross-linking density was prepared by copolymerization of methyl acrylate and ethyleneglycol dimethacrylate. The aim of this work is to study the influence of cross-linking on the conformational mobility of the polymer chains using dielectric relaxation spectroscopy (DRS) in the temperature range of the main dielectric relaxation. As expected, the temperature range in which glass transition takes place became wider with increasing crosslinking density. DRS results were analyzed using the Havriliak-Negami equation. Master Cole-Cole arcs could be drawn for all the networks. The arcs become more symmetric as cross-linking density increases, as a conseque…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsThermodynamicsGeneral ChemistryDielectricPolymerAtmospheric temperature rangePoly(methyl acrylate)chemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryRelaxation (physics)Methyl acrylateGlass transitionCole–Cole equation
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Grafted polymer layers under variable solvent conditions: A Monte Carlo simulation

1993

Polymer chains anchored with one end at a hard wall under variable solvent conditions are investigated by Monte Carlo simulations using the bond- fluctuation model. Detail information on the structural properties are obtained above, at, and below the Θ-point and discussed in terms of the appropriate theories. In particular, the scaling of the brush thickness is formulated and verified by the simulation data. For the dynamics at the Θ-point, both the relaxation time of the chain configuration and the mean-square time displacement are studied. At temperatures distinctly below the Θ-point, we find that the layer develops considerable lateral inhomogeneity in its density, which has not been pre…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsTime displacementOrganic ChemistryMonte Carlo methodMechanicsPolymerCondensed Matter PhysicsSolventChain (algebraic topology)chemistryMaterials ChemistryStatistical physicsScalingVariable (mathematics)Makromolekulare Chemie. Macromolecular Symposia
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Rheological behavior of a semirigid liquid crystal polymer

1993

The rheological behavior of liquid crystal polymers is still far from completely clarified from both experimental and theoretical points of view. In this paper, the shear flow and the non-isothermal elongation flow behavior of a semi-rigid liquid crystal copolyester is discussed. The viscosity strongly decreases when the test temperature is increased above the crystal-nematic transition temperature; below this temperature the viscosity is very high. The thermal history strongly affects the shear viscosity. The elongational flow behavior depends also on temperature. Above the crystal-nematic transition temperature and the mesophase is easily spinnable, whereas below this temperature, the spi…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsTransition temperatureMesophaseGeneral ChemistryPolymerCopolyesterPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterViscositychemistryRheologyLiquid crystalPolymer chemistryMaterials ChemistryComposite materialShear flow
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