Search results for " Plastics"

showing 10 items of 2628 documents

Synthesis of new polymers via Diels–Alder reaction. III. Biscyclohexadienephthalimides as dienes

1993

Difunctional cyclohexadienes with dihydrophthalimide central unitsand phenyl side groups to increase solubility are used as bisdienes in repetitive Diels-Alder polyadditions with bis(4-(1,2,4,-triazoline-3,5-dione-4-yl)phenyl)methane as a difunctional dienophile. The polymers show good solubility in CH 2 Cl 2 and CHCl 3 . Non-stoichiometric Diels-Alder polyaddition with slight excess of the bistriazolinedione provides the possibility of synthesizing telechelics with highly reactive triazolinedione end groups

chemistry.chemical_classificationTelechelic polymerMaterials sciencePolymers and PlasticsOrganic ChemistryCyclohexadienesPolymerMethanechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryOrganic chemistrySolubilityDiels–Alder reactionPolymer International
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Heterotelechelic Ring-Opening Metathesis Polymers

2009

By combining sacrificial synthesis with the vinyl lactone termination technique, heterotelechelic polymers were synthesized. The nonterminating nature of sacrificial synthesis was utilized to introduce a hydroxyl group at the start of the polymer chain. Lactone termination was used to functionalize the chain ends with aldehydes or carboxylic acids. The synthesis of well-defined heterotelechelic polymers was thus accomplished employing the Grubbs’ first generation catalyst as the initiator. The living nature of this polymerization allowed for precise control over the molecular weight and guaranteed full functionalization of both polymer chain ends. The presence of the functional groups is sh…

chemistry.chemical_classificationTelechelic polymerPolymers and PlasticsChemistryOrganic ChemistryPolymerRing (chemistry)MetathesisInorganic Chemistrychemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistrySurface modificationImideLactoneMacromolecules
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Synthesis of Heterotelechelic α,ω Dye-Functionalized Polymer by the RAFT Process and Energy Transfer between the End Groups

2009

The synthesis of a vinyl polymer with two different fluorescent dye end groups using reversible addition-fragmentation chain transfer (RAFT) polymerization is described. Use of a pentafluorophenyl (PFP) activated ester chain transfer agent (CTA) provided a polymer with an R end group that was reactive toward amines and a dithioester ω end group. The R PFP ester was amidated with Oregon Green Cadaverin. This did not harm the ω dithioester, which was subsequently aminolyzed with an excess of n-propylamine in the presence of Texas Red-2-sulfonamidoethyl methanethiosulfonate, resulting in a disulfide bond connecting the second dye to the polymer chain. Excess dyes and side products were removed…

chemistry.chemical_classificationTelechelic polymerPolymers and PlasticsChemistryOrganic ChemistryRadical polymerizationChain transferPolymerVinyl polymerInorganic ChemistryGel permeation chromatographyEnd-groupPolymerizationPolymer chemistryMaterials ChemistryMacromolecules
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Sacrificial Synthesis of Hydroxy-Telechelic Metathesis Polymers via Multiblock-Copolymers

2009

The synthesis of well-defined telechelic ring-opening metathesis polymers has been achieved by Sacrificial Synthesis. With the formation of cleavable triblock-copolymers, precise control over the molecular weight and the degree of functionalization was achieved. Introducing cleavable monomers that can be addressed separately, sequential deprotection was accomplished which opened the path to more sophisticated polymeric materials bearing different substituents at their respective chain ends. Sacrificial penta- and heptablock-copolymers are also presented which allow the synthesis of well-defined telechelic polymers in good yields and significantly improved initiator efficiency.

chemistry.chemical_classificationTelechelic polymerPolymers and PlasticsOrganic ChemistryMultiblock copolymerPolymerMetathesisInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistrySurface modificationAcetal copolymerImideMacromolecules
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Shear and nonisothermal elongational characterization of a liquid crystalline polymer

1989

A commercial liquid crystalline polymer (LCP) sample was characterized both in shear and in nonisothermal elongational flow over a wide range of temperatures (240–350°C). The LCP sample employed was a copolyesteramide of 2,6 hydroxynaphthoic acid, terephthalic acid, and aminophenol manufactured by Celanese and commercially known as Vectra B950. The viscosity decreases dramatically at temperatures above the crystal-nematic transition of the polymer. At lower temperatures, the extrusion of the sample is mainly due to plastic flow. Die-swell values are very small and contraction of the extrudate is also revealed, but the sample shows high elasticity. The polymer is not spinnable at very low te…

chemistry.chemical_classificationTerephthalic acidMaterials sciencePolymers and PlasticsLiquid crystallineGeneral ChemistryPolymerDie swellPlasticitychemistry.chemical_compoundShear (geology)chemistryMaterials ChemistryExtrusionComposite materialPolymer Engineering and Science
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On The Incompatibility of Dextran and Pullulan in Aqueous Solutions and Its Modeling

2012

Joint aqueous solutions of branched dextran and linear pullulan are investigated with respect to their phase separation. The experiments demonstrate that the polymers are – depending on the molar mass of dextran – incompatible in aqueous solutions despite their chemical similarity. This finding can be modeled on the basis of an approach accounting for chain connectivity and conformational relaxation of the components. According to these calculations, the polymers exhibit a miscibility gap in joint solutions despite the favorable interactions between them. Using information on the subsystems H2O/dextran and H2O/pullulan, the assumption of complete miscibility of the polysaccharides is requir…

chemistry.chemical_classificationTernary numeral systemAqueous solutionMolar massPolymers and PlasticsChemistrySpinodal decompositionOrganic ChemistryThermodynamicsPullulanPolymerCondensed Matter PhysicsMiscibilitychemistry.chemical_compoundDextranPolymer chemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Interfacial tension of demixed polymer solutions: augmentation by polymer additives

1997

The interfacial tension between phase separated polymer solutions increases pronouncedly upon the addition of asmall amounts of incompatible polymers. This feature is demonstrated by means of measurements with solutions of polystyrene in cyclohexane and the folloowing additives: poly(styrene-block-dimethylsiloxane), polyisobutylene and polydimethylsiloxane. Theoretical considerations based on a correlation between the lenth of the tie lines and the corresponding interfacial tension corroborates this finding

chemistry.chemical_classificationTernary numeral systemMaterials sciencePolymers and PlasticsCyclohexanePolydimethylsiloxaneOrganic ChemistryPolymerSurface tensionchemistry.chemical_compoundchemistryChemical engineeringPhase (matter)Polymer chemistryMaterials ChemistryCopolymerPolystyreneMacromolecular Rapid Communications
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Viscometric study on the compatibility of polymer–polymer mixtures in solution

1999

Abstract The viscosity behaviour of mixtures formed by two uncharged polymers in dilute solution has been studied at 25°C. The ternary systems assayed, and denoted solvent (1)/ polymer (2)/ polymer (3), have in common the poly(ether sulphone) (PES) as polymer 2, and poly(vinylidene fluoride) (PVDF), poly(methyl methacrylate) (PMMA) or poly(styrene) (PS) as polymer 3. The intrinsic viscosity and the viscometric interaction parameters have been experimentally measured for the binary (solvent/polymer) as well as for the ternary systems, and also theoretically evaluated for the latter. The estimation of the compatibility degree of the above polymer pairs have been done by means of three criteri…

chemistry.chemical_classificationTernary numeral systemMaterials sciencePolymers and PlasticsIntrinsic viscosityOrganic ChemistryGeneral Physics and AstronomyPolymerFlory–Huggins solution theorySolventchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryDimethylformamidePhysical chemistryMethyl methacrylateTernary operationEuropean Polymer Journal
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Viscometric behaviour of polymer blends based on poly (vinylidene fluoride)

1994

The viscosity behaviour of dilute dimethylformamide solutions of poly(vinylidene fluoride)-poly (methyl methacrylate) and poly(vinylidene fluoride)-polystyrene has been studied at 25°C. The polymer concentration ranges are such that neither phase separation nor microgel formation occurs, although we are very close to theta conditions. The intrinsic viscosity and viscosity interaction parameter of the ternary mixtures have been calculated. The estimation of the compatibility of the above polymer pairs has been studied based on: a) specific viscosities; b) viscosity interaction parameters, according to Krigbaum and Wall formalism, and c) viscosity interaction parameters of a system formed by …

chemistry.chemical_classificationTernary numeral systemMaterials sciencePolymers and PlasticsIntrinsic viscosityRelative viscosityPolymerFlory–Huggins solution theoryPhysics::Fluid DynamicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundColloid and Surface ChemistrychemistryChemical engineeringPolymer chemistryMaterials ChemistryPolymer blendPhysics::Chemical PhysicsPhysical and Theoretical ChemistryMethyl methacrylateFluorideColloid & Polymer Science
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Branched versus linear polyisoprene: Fractionation and phase behavior

2007

Abstract Branched polyisoprene (PI) was prepared from PI-macromonomers. Linear byproducts of the synthesized polymer were removed by means of inverse spin fractionation, using the solvent cyclohexane (CH) and the precipitant acetone (AC). A well-defined fraction (Mw = 17.5 kg/mol, Mw/Mn = 1.8) of the branched polyisoprene obtained in this manner was used to determine different phase diagrams with branched and/or linear PI in the mixed solvent CH/AC at 25 °C. For comparable molar masses of the polymers the two-phase area is smallest for the branched PI and slightly larger for the linear PI; in the case of the unfractionated original sample of the branched polymer one observes a pronounced pe…

chemistry.chemical_classificationTernary numeral systemMolar massPolymers and PlasticsCyclohexaneChemistryOrganic ChemistryAnalytical chemistryGeneral Physics and AstronomyPolymer architectureFractionationPolymerchemistry.chemical_compoundPhase (matter)Polymer chemistryMaterials ChemistryPolymer fractionationEuropean Polymer Journal
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