Search results for "MOLA"

showing 10 items of 1216 documents

Cylindrical Polymer Brushes with Elastin-Like Polypeptide Side Chains

2013

Monodisperse high molar mass elastin-like polypeptide macromonomers comprising 20 pentasequences (M = 8332 g/mol) were radically polymerized to high degrees of polymerization Pw = 590. Polymerization was conducted in water well above the lower phase transition temperature, i.e., in the phase separated regime. The resulting polymers adopt a cylindrical shape as demonstrated by AFM pictures of solutions spin-cast on mica. The directional persistence of the cylindrical brushes was determined by static light scattering to Kuhn statistical segments lengths lk = 120 nm at 5 mM aqueous NaCl solution which decreased to lk = 54 nm at 0.65 M NaCl. Upon polymerization the phase transition temperature …

chemistry.chemical_classificationMaterials scienceHydrodynamic radiusMolar massPolymers and PlasticsOrganic ChemistryDispersityAnalytical chemistryPolymerInorganic ChemistrychemistryPolymerizationDynamic light scatteringPhase (matter)Polymer chemistryMaterials ChemistryStatic light scatteringMacromolecules
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Crystallization Behaviour at High Cooling Rates of Two Polypropylenes

1993

Phase distribution of quenched samples of two isotactic polypropylenes, having different molecular weight distributions, was evaluated by a deconvolution procedure of WAXD spectra. The dependence on cooling rate of the two resins shows the low molecular weights rich polymer is characterized by a faster kinetics with an α-monoclinic to mesomorphic transition taking place at higher cooling rates.

chemistry.chemical_classificationMaterials scienceKineticsThermodynamicsCooling ratesPolymerSpectral linelaw.inventionchemistrylawPhase (matter)TacticityMolar mass distributionCrystallization
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Effect of the Components Molar Mass and of the Mixing Conditions on the Compatibilization of PE/LCP Blends by PE-g-LCP Copolymers

1999

The rheology, morphology, and mechanical properties of blends of high-density polyethylene (HDPE) with a semiflexible liquid crystalline copolyester (SBH) were studied in order to assess the compatibilizing ability of added PE-g-SBH copolymers, and its dependence on the molar mass of the PE matrix, and on the technique used for blend preparation. The PE-g-SBH copolymers were synthesized as described in previous articles, either by the polycondensation of the SBH monomers in the presence of a functionalized PE sample containing free carboxyl groups, or by reactive blending of the latter polymer with preformed SBH. Two samples of HDPE having different molar masses, and two samples of SBH with…

chemistry.chemical_classificationMaterials scienceMolar massCondensation polymerPolymers and PlasticscompatibilizationGeneral ChemistryPolymerCompatibilizationPolyethyleneCopolyesterSurfaces Coatings and Filmschemistry.chemical_compoundchemistrypolyethylene-LCP blendmorphologyMaterials ChemistryCopolymerrheologyHigh-density polyethyleneComposite material
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Interfacial Tensions from Drop Retraction versus Pendant Drop Data and Polydispersity Effects

2004

Interfacial tensions sigma were measured by means of both methods for the following polymer pair: polyisobutylene (PIB 3) plus poly(dimethylsiloxane) (PDMS 152) and poly(dimethyl-co-methylphenylsiloxane) (CoP26*) plus PDMS 48. The numbers after the abbreviation state the molar masses in kilograms; the homopolymers exhibit polydispersities on the order of 2. The reliability of the method of drop retraction is backed up by systematic measurements, which demonstrate that it is possible to study the time evolution of sigma. Because of the free choice of the phases (drop or matrix) and the possibility to vary the overall composition of the system in a wide range, drop retraction yields more info…

chemistry.chemical_classificationMaterials scienceMolar massDrop (liquid)DispersityTime evolutionThermodynamicsSurfaces and InterfacesPolymerCondensed Matter PhysicsDrop methodSurface tensionchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceSpectroscopyLangmuir
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Detection of polymer compatibility by means of self-organization: poly(ethylene oxide) and poly(sodium 4-styrenesulfonate)

2021

Information on the miscibility of different polymers A and B on a molecular level is important in many ways. However, along the traditional lines this knowledge is difficult and time consuming to achieve. The current study presents a simple alternative, based on the determination of the intrinsic viscosities (specific hydrodynamic volume of isolated coils) for blend solutions in a common solvent. In the case of incompatible polymers, isolated coils contain one macromolecule only, either A or B. In contrast, compatible polymers form mixed isolated coils, because of favorable interactions. The present investigation was carried out for the system water/poly(ethylene oxide)/poly(sodium 4-polyst…

chemistry.chemical_classificationMaterials scienceMolar massEthylene oxideOxide02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesMiscibilityPolyelectrolyte0104 chemical scienceschemistry.chemical_compoundSulfonatechemistryChemical engineering0210 nano-technologyMacromoleculeSoft Matter
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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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