Search results for "plastics"

showing 10 items of 2724 documents

Phase equilibria and interfacial tension between coexisting phases for the system water/2-propanol/poly(acrylic acid)

1995

The cloud point curve, tie-lines and interfacial tensions were measured for solutions of 50 mol-% neutralized (counter-ion Na ○+ ) poly(acrylic acid) (molar mass M w = 9 700 g/mol; polydispersity index M w /M n = 2,0) in the mixed solvent water/2-propanol at 30°C. Due to the non-uniformity of the polymer, the end-points of the tie-lines are not situated on the cloud-point curve. The interfacial tension σ, determined by means of the spinning drop method, increases in sigmoidal manner with R tl , the length of the tie-line, expressed in terms of weight fractions. An evaluation of these data in a double-logarithmic plot of σ.M -0,5 versus R tl yields a critical exponent of 4,23 as compared wit…

Molar massPolymers and PlasticsOrganic ChemistryDispersityCondensed Matter PhysicsToluenePropanolSurface tensionchemistry.chemical_compoundchemistryPhase (matter)Polymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryMass fractionAcrylic acidMacromolecular Chemistry and Physics
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Apparent Molar Mass of a Polyelectrolyte in an Organic Solvent in the Low Ionic Strength Limit As Revealed by Light Scattering

2013

The apparent molar mass of a partially quaternized poly-2-vinylpyridines (degree of quaternization 4.3% < Q < 35%) in 1-propanol is measured by light scattering at low ionic strength (10–6 M < cs < 10–3 M) as a function of polyion repeat unit concentration (7 × 10–5 monomol/L < cm,p < 4 × 10–2 monomol/L). No dialysis was applied prior to measurements. The apparent molar mass under “salt-free” conditions is smaller than the true molar mass by an order of magnitude, while approaching the true value at higher ionic strength. Concomitant data on the dependence of scattering intensity on scattering wave vector show that the dilute polyelectrolyte solutions are strongly correlated. A recent theor…

Molar massPolymers and PlasticsScatteringChemistryOrganic ChemistryInorganic chemistryAnalytical chemistryApparent molar propertyLight scatteringPolyelectrolyteInorganic ChemistryAbsolute molar massIonic strengthMaterials ChemistryMolar mass distributionMacromolecules
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1995

About 340 g of a cycloaliphatic ionene (see formula given in the introduction) were fractionated by a continuous countercurrent extraction method (CPF). The efficiency of the separation was checked by viscometry and gel permeation chromatography (GPC). Ten different fractions with number average molecular masses between 16 000 and 29 000 D were obtained and their glass transition temperatures T g determined by differential scanning calorimetry (DSC) for their bromide and tetrafluoroborate salts. No molecular weight dependence of T g was found, in contrast to recently reported results with aliphatic ionenes, where - in case of the bromide - T g increases with rising molecular weight.

Molar massTetrafluoroboratePolymers and PlasticsGeneral Chemical EngineeringAnalytical chemistryFractionationPolyelectrolyteGel permeation chromatographychemistry.chemical_compoundDifferential scanning calorimetrychemistryBromideOrganic chemistryGlass transitionActa Polymerica
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Nebenreaktionen der radikalisch ausgelösten Cyclisierung von 2,2′-Methylen-bis(4-methyl-1,2-phenylen)-dimethacrylat

1979

2,2′-Methylene-bis(4-methyl-1,2-phenylene) dimethacrylate (1) was reacted with an excess of 2,2′-azoiso-butyronitrile (mole ratio 1:15) highly diluted in boiling benzene. The reaction products were separated by column chromatography. It was found that the 1-cyano-1-methylethyl radical induced the cyclization of 1 to yield the product of a head to tail addition (2) in 55% yield. In addition, the product of a head to head addition (3) was isolated in 4% yield. 35% of 1 reacted in the same way as it has already been observed as suppression of polymerization in the case of p-tolyl methacrylate to give the products 4 and 5. The structures of the products were confirmed by elemental analyses, by …

Mole ratioPolymers and PlasticsChemistryHead to headMethacrylateMedicinal chemistrychemistry.chemical_compoundColloid and Surface ChemistryColumn chromatographyPolymerizationYield (chemistry)Polymer chemistryMaterials ChemistryProton NMRPhysical and Theoretical ChemistryBenzeneColloid and Polymer Science
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Low molecular chemistry and its effect on macromole chemistry

1965

Molecular chemistryPolymers and PlasticsChemistryMaterials ChemistryNanotechnologyGeneral ChemistryChemistry (relationship)Polymer Engineering and Science
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Influence of chain length on the molecular dynamics of an aliphatic ionene

1998

An aliphatic random copolymer ionene (a cationic polyelectrolyte with N + in the repeat unit), was fractionated with the continuous polymer fractionation and investigated for its molecular weight dependent properties. The fractions were analyzed with GPC and capillary viscometry for their molecular weight. Glass transition temperatures were determined with DSC and a strong molecular weight dependence was observed, but no influence in the ionic conductivity was observed. The temperature dependency of ionic conductivity in ionenes is described.

Molecular dynamicsPolymers and PlasticsChemistryGeneral Chemical EngineeringPolymer chemistryCationic polymerizationCopolymerPhysical chemistryViscometerIonic conductivityPolymer fractionationGlass transitionPolyelectrolyteActa Polymerica
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Effect of Elongational Flow and Polarity of Organomodified Clay on Morphology and Mechanical Properties of a PLA Based Nanobiocomposite

2016

Abstract In biodegradable polymer world nanobiocomposites represent a new group of materials filled with inert nanoparticles that shows very interesting properties and the biodegradability of the matrix. In this work we have studied the effect of the polarity of the organomodified montmorillonite and of the elongational flow on the morphology and the rheological and mechanical properties of a new nanobiocomposite with a matrix of biodegradable PLA based blend. The elastic modulus enhances in presence of the nanofiller and this increase is larger and larger with the increment of the orientation. The tensile strength does not show any significant change at the same level of orientation. Moreo…

Morphology (linguistics)Materials scienceNanocompositePolymers and PlasticsElongational flow nanobiocompositeGeneral Chemical EngineeringNanoparticle02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiodegradable polymerIndustrial and Manufacturing Engineering0104 chemical scienceschemistry.chemical_compoundMontmorillonitechemistryRheologyUltimate tensile strengthMaterials ChemistryComposite material0210 nano-technologyElastic modulusInternational Polymer Processing
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Co-Assembly of A–B Diblock Copolymers with B′-type Nanoparticles in Thin Films: Effect of Copolymer Composition and Nanoparticle Shape

2014

The coassembly of A–B diblock copolymers with B′-type nanoparticles (i.e., nanoparticles that are slightly incompatible with the B domain) leads to hierarchical structures, where the block copolymer phase separates first and the nanoparticles create close-packed arrays within the B domains due to a slower, secondary phase separation process. Here we report the results of a comprehensive study, which focused on two aspects: the influence of the nanoparticle shape (spherical vs rod-like) and the effect of the volume composition of the blocks. Three polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) copolymers featuring similar molecular weights but differing in PS volume fraction were mi…

Morphology (linguistics)Materials sciencePolymers and PlasticsEthylene oxideOrganic ChemistryNanoparticleInorganic Chemistrychemistry.chemical_compoundchemistryChemical engineeringPhase (matter)Volume fractionPolymer chemistryMaterials ChemistryCopolymerMethyl methacrylateThin filmMacromolecules
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Comparative Study of Different Maleic Anhydride Grafted Compatibilizer Precursors toward LDPE/PA6 Blends: Morphology and Mechanical Properties

2005

The study deals with the effectiveness of maleic anhydride grafted styrene-b-ethylene-co-propylene copolymer (SEPMA) as compatibilizer precursor (CP) for blends of low density polyethylene (LDPE) with polyamide-6 (PA). The CP was produced by grafting MA onto SEP in the melt. The specific interactions between the CP and the blends components have been investigated through characterizations of the binary LDPE/CP and PA/CP blends. The compatibilizing efficiency of the MA-grafted SEP, as revealed by the thermal properties and the morphology of the compatibilized blends, has been shown to be excellent. The morphology, as well as the mechanical properties of the compatibilized with SEPMA 75/25 w/…

Morphology (linguistics)Materials sciencePolymers and PlasticsOrganic ChemistryMaleic anhydrideConcentration effectGraftingmorphology and mechanical propertiesLDPE/PA6 blendchemistry.chemical_compoundLow-density polyethylenechemistryChemical engineeringMA-functionalized compatibilizer precursorMaterials ChemistryCopolymerPolymer blendHigh-density polyethyleneComposite material
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Phenomenological approach to compare the crystallization kinetics of isotactic polypropylene and polyamide-6 under pressure

2001

Reliable experimental data for semicrystalline polymers crystallized under pressure are supplied on the basis of a model experiment in which drastic solidification conditions are applied. The influence of the pressure and cooling rate on some properties, such as the density and microhardness, and on the product morphology, as investigated with wide-angle X-ray scattering (WAXS), is stressed. Results for isotactic polypropylene (iPP) samples display a lower density and a lower microhardness with increasing pressure over a wide range of cooling rates (from 0.01 to 20 °C/s). Polyamide-6 (PA6) samples exhibit the opposite behavior, with the density and microhardness increasing at higher pressur…

Morphology (linguistics)Materials sciencePolymers and PlasticsThermodynamicsIndentation hardnessCrystallinityPhase (matter)TacticityPolymer chemistryMaterials ChemistryPressurePolyamides (PA6)Physical and Theoretical Chemistrychemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaScatteringCooling rateSettore ING-IND/34 - Bioingegneria IndustrialePolymerCondensed Matter PhysicsKineticsSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryPolyamidePoly(propylene) (PP)Crystallization
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