Search results for "Plastics"

showing 10 items of 2724 documents

Structure evolution and reaction mechanism in the Ni/Al reactive multilayer nanofoils

2014

Abstract The extremely rapid gasless reactions in binary Ni/Al reactive multilayer nanofoils (RMNFs) are investigated both experimentally and theoretically. The quenching technique is used to study the dynamics of structural transformation on the micro- and nanoscales. The experimentally obtained patterns of structural evolution related to the heterogeneous reactions are compared with the results of molecular dynamics simulations carried out for the same reactive system. Based on the obtained data, the intrinsic mechanism of the reaction in Ni/Al RMNF is considered, which adequately explains the unusual parameters of a gasless combustion wave in such a system.

QuenchingReaction mechanismMaterials sciencePolymers and PlasticsMetals and AlloysCombustionStructural evolutionStructural transformationElectronic Optical and Magnetic MaterialsMolecular dynamicsComputational chemistryChemical physicsCeramics and CompositesReactive systemActa Materialia
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Kinetics of phase separation in polymer blends for deep quenches

1986

Electro microscopy was used to study the phase separation kinetics of a polystyrene/polyvinylmethylether system subjected to a critical deep quench. The size of the phase-separated domains was found to increase linearly with time, implying that hydrodynamic effects control the rate of growth of the domains in the time scale and temperature range under consideration. From these measurements the growth velocity and approximate diffusion constants can be determined for three different temperatures. Comparison of these results with those obtained by light scattering on other systems and with theoretical predictions is possible by replotting in dimensionless units.

QuenchingSpinodalPolymers and PlasticsChemistryKineticsMineralogyThermodynamicsAtmospheric temperature rangeCondensed Matter PhysicsLight scatteringchemistry.chemical_compoundCritical point (thermodynamics)Materials ChemistryPolystyrenePhysical and Theoretical ChemistryDimensionless quantityJournal of Polymer Science Part B: Polymer Physics
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The X-ray determination of the amounts of the phases in samples of isotactic poly(propylene) quenched from the melt at different cooling rates

1997

A new procedure for the determination of the amounts of phases in samples of isotactic poly(propylene) quenched at different cooling rates from the same melted polymer is described. According to the procedure, all the patterns corresponding to the same quenching series are simultaneously analyzed for the amounts of phases so that reliable phase fractions relative to the different samples of the series are achieved. The analysis of the results points out that for increasing cooling rates above 30°C/s a remarkable increase of the mesomorphic phase settles, mainly at the expense of the α-monoclinic one.

Quenchingchemistry.chemical_classificationMaterials sciencePolymers and PlasticsStereochemistryOrganic ChemistryAnalytical chemistryX-rayCooling ratesPolymerCondensed Matter PhysicschemistryPhase (matter)TacticityPolymer chemistryMaterials ChemistryPhysical and Theoretical Chemistry
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Dielectric behaviour of a γ-irradiated polycarbonate

1980

Dielectric measurements on a γ-irradiated polycarbonate in a dose range 0–20 Mrad and at test frequencies of 103 and 104 Hz have been carried out. The glass transition temperature shows a maximum at 3.5 Mrad and then decreases at larger doses. This result is in line with other experiments (intrinsic viscosity, dynamic-mechanical measurements, etc) already reported: the Tg values are however larger in the present results. This is probably due to the plasticizing action of the absorbed moisture present in the previous tests. A Tg vs 1/[n]2 plot (1/[n]2 is proportional to 1/m ) allows to find the value of the glass transition point at an infinite molecular weight and the dependency of Tg on mo…

Range (particle radiation)Materials sciencePolymers and PlasticsMoistureIntrinsic viscosityAnalytical chemistryGeneral ChemistryDielectricCondensed Matter Physicsvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumIrradiationPolycarbonateGlass transitionLine (formation)Polymer Bulletin
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Molecular dynamics in low-molar and polymeric ferroelectric liquid crystals

1991

Broadband dielectric spectroscopy covering the frequency range from 10−1 Hz to 109 Hz was employed to study the molecular dynamics in low-molar and polymeric ferrroelectric liquid crystals. At frequencies below 106 Hz the ferroelectric modes, soft and Goldstone mode are observed. In the frequency regime from 106 Hz to 109 Hz a fast relaxation process is found, which is assigned to the hindered rotation of the mesogens around their long molecular axis. It turns out that the molecular dynamics is not principally different between low-molar and polymeric systems.

Range (particle radiation)Materials sciencePolymers and PlasticsOrganic ChemistryMolecular axisCondensed Matter PhysicsRotationFerroelectricityMolecular physicsMolecular dynamicsNuclear magnetic resonanceLiquid crystalvisual_artMaterials Chemistryvisual_art.visual_art_mediumGoldstoneBroadband dielectric spectroscopyMakromolekulare Chemie. Macromolecular Symposia
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Monte Carlo simulation of micelle formation in block copolymer solutions

1998

Short block copolymers in selective solvents (bad for A-block, good for B-block) are modeled by flexible bead-spring chains, where beads interact with short range Morse potentials of variable strength. It is shown that already very short chains (N A = N B = 2) exhibit a rather well-defined critical micelle concentration (cmc). The mass distribution of the micelles and their gyration tensor components as well as their internal structure are studied. It is shown that the relaxation time increases exponentially with the strength E AA of the attractive energy between the A-monomers, and thus frozen-in micelles of medium size are obtained when E AA is chosen too large. Our results are compared t…

Range (particle radiation)Polymers and PlasticsMass distributionChemistryOrganic ChemistryMonte Carlo methodThermodynamicsGyration tensorCondensed Matter PhysicsMicelleInorganic ChemistryCritical micelle concentrationMaterials ChemistryCopolymerPhysical chemistryMacromolecular Theory and Simulations
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Die Synthese reiner Oligo[hydroxy-5-nitro1,3-phenylen)-methylen]e, Verbindungen mit mehreren ortho- bzw. para-Nitrophenolbausteinen im Molekül

1976

Zur Synthese der Oligo[(hydroxy-5-nitro-1,3-phenylen)methylen]e dienten chlormethylierte Nitrophenole sowie mono- und bischlormethylierte Bis- und Tris[(hydroxy-5-nitro-1,3-phenylen)methylen]e. Die Chlormethylierung erfolgte durch Umsetzung mit Chlormethylmethylather in Gegenwart von Zinkchlorid. Die Synthese der Oligomeren gelang mit guten Ausbeuten, wenn die chlormethylierten Verbindungen mit stark uberschussigem Nitrophenol und Zinkchlorid als Katalysator kondensiert wurden. Reaktionsbedingungen und unterschiedliche Reaktionsfahigkeiten werden mitgeteilt. Einige Verbindungen wurden in ihrer Struktur bestatigt, indem sie auf zwei voneinander unabhangigen Wegen dargestellt wurden. Damit wa…

Reaction conditionsTrisPolymers and PlasticsChemistrychemistry.chemical_elementZincMedicinal chemistryCatalysischemistry.chemical_compoundNitrophenolColloid and Surface ChemistryPolymer chemistryMaterials ChemistryMethylenePhysical and Theoretical ChemistryChloromethyl methyl etherColloid and Polymer Science
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The effect of reaction conditions on the chain end structure and functionality during dehydrochlorination oftert-chlorine-telechelic polyisobutylene …

1998

Dehydrochlorination of tert-chlorine-telechelic polyisobutylene with potassium tert-butoxide in refluxing tetrahydrofuran is quantitative after 22 h, but results in ca. 3% endo olefin chain ends which are not reactive in some subsequent functionalization reactions. The formation of these undesired structures is most likely due to simultaneous thermally induced HCl loss. Lower temperatures and longer reaction times led to exclusive formation of external double bonds in some cases but to incomplete dehydrochlorination.

Reaction conditionschemistry.chemical_classificationOlefin fiberPolymers and PlasticsDouble bondPotassiumOrganic Chemistrychemistry.chemical_elementchemistry.chemical_compoundchemistryChain (algebraic topology)Potassium tert-butoxidePolymer chemistryMaterials ChemistrySurface modificationTetrahydrofuranMacromolecular Rapid Communications
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Photooxidative behaviour of polyethylene/polyamide-6 blends

2010

International audience; The photochemical behaviour of several polyethylene/polyamide-6 blends was studied under conditions of artificial accelerated weathering. Particular attention was paid to five different compositions ranging from pure polyethylene to pure polyamide with blends of PE/PA-6 of various compositions: 75/25, 50/50 and 25/75 wt/wt%. Analysis by infrared spectroscopy of the chemical modifications caused by photooxidation showed that exposing the polyethylene/polyamide-6 blends to UV-light irradiation led to the formation of oxidation photoproducts in both polymer phases. In agreement with both the mechanical and spectroscopic analyses, the photooxidation rate of the blends wa…

Reaction mechanismMaterials sciencePolymers and PlasticsInfrared spectroscopy02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundPhase (matter)Polymer chemistryMaterials ChemistryIrradiationchemistry.chemical_classificationPolymer blendPolymerPolyethylene021001 nanoscience & nanotechnologyCondensed Matter PhysicsPhotooxidation behaviour0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymerschemistryChemical engineeringInfrared analysisMechanics of MaterialsPolyamidePolymer blend0210 nano-technologyMechanical propertie
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Step growth polymerization via tandem ene and diels-alder reactions

1997

In contrast to other electron deficient enophiles or dienophiles which react with 1,4-cyclohexadiene (1,4-CHD) under aromatization, 1,2,4-triazoline-3,5-diones react in a defined reaction sequence. In a first step the 1,4-cyclohexadiene reacts via an ene-reaction. The intermediately formed substituted 1,3-cyclohexadiene immediately reacts in a Diels-Alder reaction. The regiochemistry of the Diels-Alder reaction is controlled by the solvent polarity. This reaction sequence can be used to synthesize polymers. Low-molar-mass model compounds were synthesized to elucidate the stereochemistry of the polymers. By varying the bistriazolinedione, polymers with backbones of different rigidity are ava…

Reaction mechanismPolymers and PlasticsChemistryOrganic ChemistryAromatizationRegioselectivityCondensed Matter PhysicsStep-growth polymerizationchemistry.chemical_compoundCascade reactionPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistrySolvent effectsImideEne reactionMacromolecular Chemistry and Physics
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