Search results for "Molar"

showing 10 items of 1069 documents

Different kinds of solid solutions in the V2O5-ZrSiO4-NaF system by sol-gel processes and their characterization

1993

Abstract In the V2O5-ZrSiO4-NaF system, three kinds of substances have been identified by sol-gel methods depending on the V2O5 amounts in the composition. Their characterization by X-ray diffraction, measurements of unit cell parameters, UV-visible (UV-V) spectroscopy, differential thermal analysis and lab colour parameter determination allow the consideration of three kinds of solid solution in the zircon lattice: (a) V+5,V+4-ZrSiO4, thermally stable and with a deep green colour; (b) V+4-ZrSiO4, thermally stable and blue coloured, made by the sol-gel method and with V2O5 amounts lower than 0·03 mol per formula weight; and (c) Na+,F−,V+4-ZrSiO4, a solid solution with a deep blue-turquoise …

chemistry.chemical_classificationMaterials scienceMolar massInorganic chemistryAnalytical chemistrychemistry.chemical_compoundchemistryDifferential thermal analysisZirconium(IV) silicateX-ray crystallographyMaterials ChemistryCeramics and CompositesQualitative inorganic analysisChemical compositionInorganic compoundSolid solutionJournal of the European Ceramic Society
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Compatibilization of blends of polyethylene with a semirigid liquid crystalline polymer by PE-g-LCP copolymers

1997

The blends of thermoplastics with liquid crystalline polymers show, in general, poor properties because of the lack of adherence between the two phases. The use of ad hoc synthesized copolymers containing the monomer units of the two polymers has been recently considered by some of us for blend compatibilization, and the results appear promising. In this work, new PE-g-LCP copolymers, prepared either by the synthesis of the LCP in the presence of a functionalized PE, or by reactive blending of the latter polymer with preformed LCP, have been employed as compatibilizing additives for blends of PE with a semirigid LCP. The morphology and the rheological and mechanical properties of the ternar…

chemistry.chemical_classificationMaterials scienceMolar massPolymers and PlasticsCOMPATIBILIZATIONMaleic anhydrideGeneral ChemistryCompatibilizationPolymerPolyethyleneBLENDSCOPOLYMERSchemistry.chemical_compoundMonomerSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryChemical engineeringLiquid crystalMaterials ChemistryCopolymerMORPHOLOGYComposite materialPOLYPROPYLENEFIBERS
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Transparent thermoplastic polyurethanes based on aliphatic diisocyanates and polycarbonate diol

2016

Segmented thermoplastic polyurethanes (PUs) were synthetized using polycarbonate diol as soft segment with a molar mass of 500 and as a hard segment 1,5-pentanediol with a combination of isophorone diisocyanate (IPDI) and hexamethylene diisocyanate (HDI). Differential scanning calorimetry, differential mechanical analysis, Fourier transform infrared-attenuated total reflection spectroscopy, haze, transmittance, hardness, tensile properties and retention of tensile properties tests were employed to characterize the different PUs. The results of this study show that IPDI/HDI relation has a significant impact on the phase mixing, crystallinity and therefore on the PU’s properties. The variati…

chemistry.chemical_classificationMaterials scienceMolar massThermoplasticPolymers and PlasticsDiol02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallinityDifferential scanning calorimetrychemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumHexamethylene diisocyanateComposite materialPolycarbonateIsophorone diisocyanate0210 nano-technologyJournal of Elastomers & Plastics
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Structure formation in doped discotic polymers and low molar mass model systems

1992

Abstract Doping of low molar mass materials or polymers, possessing disc-like units, with electron acceptors leads to the stabilization of columnar discotic phases or even to the induction of such phases in compounds which either display a nematic discotic phase or only an amorphous phase in the absence of the electron acceptor. The induced columnar phase corresponds frequently to a hexagonally ordered one. We have observed, however, in addition the induction of new columnar phases such as the rectangularly ordered (Dro) and the columnar nematic phase (Nc). The enhancement of the tendency towards the formation of columnar phases is a consequence of electron acceptor—electron donor complex f…

chemistry.chemical_classificationMaterials scienceMolar massgenetic structuresDiscotic liquid crystalDopingGeneral ChemistryPolymerElectron acceptorCondensed Matter PhysicsCrystallographychemistryLiquid crystalPhase (matter)General Materials ScienceColumnar phaseLiquid Crystals
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Rheological characterization of polycaprolactam anionically synthesized in the presence of lithium chloride

1980

Melt viscosity and dynamic-mechanical data are reported for samples obtained by anionic polymerization of caprolactam, in the presence of LiCl. The full body of results is essentially in line with those previously reported relative to mixtures of inorganic salts and commercial nylon 6, In particular a drastic-decrease of the melting point and of the rate of crystallization is confirmed as well as an increase of the glass transition temperature and of the melt viscosity. Some quantitative differences exist, which may be attributed to the different molecular weight distribution in the polymers employed in the present work.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsCaprolactamGeneral ChemistryPolymerlaw.inventionchemistry.chemical_compoundNylon 6chemistryChemical engineeringlawPolymer chemistryMaterials ChemistryMelting pointLithium chlorideMolar mass distributionCrystallizationGlass transitionPolymer Engineering and Science
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Relative strength of H-bonding groups on biodegradable polymer-based blends in solution

2006

The intermolecular hydrogen bonding interactions between poly(3-hydroxybutyrate) and poly(styrene-co-vinyl phenol) copolymers with mutual solvent epichlorohydrin were thoroughly investigated by steady-state fluorescence and viscosity techniques. Fluorescence spectroscopy along with viscosity technique was used to asses the intermolecular hydrogen bonding between poly-(3-hydroxybutyrate) and its blends with five copolymer samples of styrene–vinyl phenol, containing different proportions of vinyl phenol but similar average molecular weight and polydispersity index. In the case of very low OH contents (2–4 mol %), as expected, both components of poly(3-hydroxybutyrate) and poly(styrene-co-4-vi…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsDispersityAnalytical chemistryGeneral ChemistryPolymerFlory–Huggins solution theoryFluorescence spectroscopySurfaces Coatings and FilmsSolventchemistryPolymer ratioPolymer chemistryMaterials ChemistryMolar mass distributionPolymer blendJournal of Applied Polymer Science
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Specialty and advanced polymers by carbocationic macromolecular engineering

1993

This study briefly surveys a variety of new advanced polymeric materials and controlled synthetic processes available by carbocationic macromolecular engineering techniques and having potential commercial interest. These recent developments, mainly by living carbocationic polymerization, have led to new opportunities in polymerization process control, and in designing microstructure, functionality, molecular weight and molecular weight distribution (MWD) and thus properties of a wide variety of unique polymer systems. The fundamentals of these new emerging technologies and the novel materials offered by them, such as macromonomers, telechelics, polymers with pendant functional groups (liqui…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsLiquid crystallineOrganic ChemistryNanotechnologyPolymerCondensed Matter PhysicschemistryPolymerizationOptical materialsAmphiphileMaterials ChemistryCopolymerOrganic chemistryMolar mass distributionMacromoleculeMakromolekulare Chemie. Macromolecular Symposia
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Polydispersity and Molecular Weight Distribution of Hyperbranched Graft Copolymers via “Hypergrafting” of ABm Monomers from Polydisperse Macroinitiat…

2013

The hypergrafting strategy designates the synthesis of hyperbranched graft copolymers (HGCs) in a grafting-from approach, using ABm monomers, from multifunctional, polydisperse macroinitiator cores by slow monomer addition. Hypergrafting leads to complex polymer topologies with defined molecular weight, degree of branching (DB), and polydispersity (PD). By a generating function formalism, a generally applicable equation for the PD of HGCs (PD = PDf + (m – 1)/f) is derived, where PDf is the polydispersity of the core and f its average functionality. In addition, the complete molecular weight distribution function has been calculated for varied m and f as well as for a given distribution of i…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryDispersityModel systemPolymerBranching (polymer chemistry)Inorganic Chemistrychemistry.chemical_compoundFormalism (philosophy of mathematics)MonomerChemical engineeringchemistryPolymer chemistryMaterials ChemistryCopolymerMolar mass distributionMacromolecules
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Time-resolved rheology as a tool to monitor the progress of polymer degradation in the melt state - Part I: Thermal and thermo-oxidative degradation …

2015

Abstract Thermal and thermo-oxidative degradation of polyamide 11 (PA11) in the melt state (T = 215 °C) are studied by resorting to time-resolved mechanical spectroscopy. Such an approach allows to elude the changes in the rheological properties occurring while testing, thus enabling the rigorous study of polymer degradation in the melt state. Different concurrent degradation reactions in oxidative (air) and non-oxidative (N2) environment are promptly guessed by studying the time evolutions of rheological functions. In particular, changes in the zero-frequency complex viscosity reflects changes in the average molecular weight, while the appearance of a yield stress in the complex viscosity …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsRheometryOrganic ChemistrySize-exclusion chromatographyPolymerSECSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiPolymer degradationChemical engineeringRheologychemistryMALDI- TOF-MSPolyamideThermal degradationThermo-oxidative degradationMaterials ChemistryOrganic chemistryDegradation (geology)Molar mass distributionRheologyPolyamide 11
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Melt Strength and Extensibility of High-Density Polyethylene

1984

The extensional flow of polymer melts has been extensively studied because of its importance in many technological processing operations and, from a more fundamental point of view, because the tensile properties of the polymer melts cannot be correlated directly with shear viscosity behavior.1–5

chemistry.chemical_classificationMaterials sciencechemistryShear viscosityUltimate tensile strengthFlow (psychology)Molar mass distributionPoint (geometry)High-density polyethylenePolymerComposite materialExtensibility
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