Search results for "Copolymer"

showing 10 items of 1003 documents

Tomographic and Topographic Investigation of Poly-D,L-Lactide-Co-Glycolide Microspheres Loaded with Prostaglandine E<sub>2</sub> for Exte…

2010

Polymeric, biodegradable microspheres represent a good reliable system to investigate the release of bioactive substances in both in vitro and in vivo applications. Common biomaterials for the synthesis of these microspheres are aliphatic polyesters of the poly(α-hydroxy)acids, especially poly-L-lactides (PLA) and polyglycolides (PGA) or their copolymers poly-D,L-lactide-co-glycolides (PLGA). In our own previous studies we have developed PLGA microspheres with integrated PGE2 as model substance for a wide range of biomedical applications, especially in angiogenesis, fracture healing and cartilage repair. The synthesis is based on a binary solvent in water emulsion approach, where two differ…

chemistry.chemical_classificationMaterials scienceGeneral EngineeringEthyl acetateAnalytical chemistryPolymerHigh-performance liquid chromatographyPolyesterSolventchemistry.chemical_compoundPLGAchemistryChemical engineeringEmulsionCopolymerAdvanced Materials Research
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Statistical properties of linear-hyperbranched graft copolymers prepared via "hypergrafting" of AB(m) monomers from linear B-functional core chains: …

2015

The reaction of ABm monomers (m = 2, 3) with a multifunctional Bf-type polymer chain ("hypergrafting") is studied by coarse-grained molecular dynamics simulations. The ABm monomers are hypergrafted using the slow monomer addition strategy. Fully dendronized, i.e., perfectly branched polymers are also simulated for comparison. The degree of branching of the molecules obtained with the "hypergrafting" process critically depends on the rate with which monomers attach to inner monomers compared to terminal monomers. This ratio is more favorable if the ABm monomers have lower reactivity, since the free monomers then have time to diffuse inside the chain. Configurational chain properties are also…

chemistry.chemical_classificationMaterials scienceHydrodynamic radiusGeneral Physics and AstronomyThermodynamicsPolymerBranching (polymer chemistry)Molecular dynamicschemistry.chemical_compoundMonomerchemistryPolymer chemistryCopolymerRadius of gyrationPolymer blendPhysical and Theoretical ChemistryThe Journal of chemical physics
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Fabrication of a Silica Coating on Magnetic γ-Fe2O3 Nanoparticles by an Immobilized Enzyme

2008

Silicatein, a hydrolytic protein encountered in marine sponges, was immobilized on maghemite (γ-Fe2O3) nanoparticles that were surface functionalized with a reactive mulfunctional polymer. This polymer carries an anchor group based on dopamine which is capable of binding to the γ-Fe2O3 surface and a reactive functional group which allows binding of various biomolecules onto inorganic nanoparticles. This functional nitrilotriacetic acid (NTA) group allows immobilization of His-tagged silicatein on the surface of the γ-Fe2O3 nanoparticles. The surface-bound protein retains its native hydrolytic activity to catalyze formation of silica through copolymerization of alkoxysilanes Si(OR)4. Functio…

chemistry.chemical_classificationMaterials scienceImmobilized enzymeGeneral Chemical EngineeringBiomoleculeInorganic chemistryNitrilotriacetic acidMaghemiteNanoparticleGeneral Chemistryengineering.materialchemistry.chemical_compoundchemistryChemical engineeringMaterials ChemistryengineeringCopolymerMagnetic nanoparticlesSurface modificationChemistry of Materials
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Laponite clay in homopolymer and tri-block copolymer matrices

2007

Macromolecule/laponite nanomaterials were studied by DSC and X-ray diffraction techniques. The matrices are poly(ethylene) glycols at various molecular masses and poly(ethylene oxides)-poly(propylene oxides)-poly(ethylene oxides) tri-block copolymers. The latter were tuned by modulating the molecular masses, at constant hydrophilic/hydrophobic ratio, and the hydrophilicity. For all the investigated systems, the enthalpy of melting (ΔH m) is nearly constant up to a given composition thereafter it increases monotonically reaching the value of the pure macromolecule. We proposed a model to interpret the DSC data. Briefly, it was invoked a mechanism of interaction following which some segments …

chemistry.chemical_classificationMaterials scienceIntercalation (chemistry)EnthalpyPolymerCondensed Matter Physicsdispersion in polymer matrices DSC laponite poly(ethylene)glycols poly(ethylene oxide)poly(propylene oxide)poly(ethylene oxide) X-ray diffractionDifferential scanning calorimetrychemistryChemical engineeringPolymer chemistryX-ray crystallographyCopolymerPhysical and Theoretical ChemistryThermal analysisMacromoleculeJournal of Thermal Analysis and Calorimetry
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Dye-containing S∗cside-on/end-on copolymers

1995

Abstract Mesomorphic copolysiloxanes, which combine ‘normal’ end-on linked chiral mesogenic units inducing S∗c phases and side-on fixed chromophores were prepared. The interplay of the different orientational tendencies of these moieties, which are perpendicular (end-on linked mesogenic groups) or parallel (side-on fixed chromophores) to the polymer chain, lead to a strong destabilization of the S∗c phase. However, copolymers with up to about 10 mol % of chromophores still show a smectic C∗ phase. FTIR measurements show that both moieties orient parallel to each other and perpendicular to the polymer chains. These copolymers are interesting to consider as coloured guest-host S∗c materials f…

chemistry.chemical_classificationMaterials scienceMesogenGeneral ChemistryPolymerChromophoreCondensed Matter PhysicsCrystallographychemistryLiquid crystalPhase (matter)CopolymerPerpendicularOrganic chemistryGeneral Materials ScienceFourier transform infrared spectroscopyLiquid Crystals
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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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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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EVA copolymer based nanocomposites: rheological behavior under shear and isothermal and non-isothermal elongational flow

2006

Abstract Nanocomposites are a very promising new class of polymer composites that exhibit an interesting combination of chemical, physical and mechanical properties. Only small amounts of nanofiller are sufficient to generate great variation of many properties. This work focuses on the rheological properties of poly[ethylene- co -(vinyl acetate)] (EVA copolymer) based nanocomposites in shear and in isothermal and non-isothermal elongational flow. The nanocomposites, at two different filler contents, were prepared in two different extruders and intercalates were obtained for all the samples. The twin-screw compounder is more efficient. The change of rheological properties, both in shear and …

chemistry.chemical_classificationMaterials scienceNanocompositePolymers and PlasticsOrganic ChemistryPolymerSilicateIsothermal processchemistry.chemical_compoundShear (geology)chemistryRheologyCopolymerVinyl acetateComposite material
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Liquid crystalline phases from polymer functionalized ferri-magnetic Fe3O4nanorods

2017

Here, we present the surface functionalization of anisotropic in form ferri-magnetic Fe3O4-nanorods (NRs) with a diblock copolymer, having a PMMA- or PDEGMEMA-block, for solubilization, and a dopamine anchor block. These polymers were synthesized through RAFT polymerization via a macro-initiator approach. The successful surface functionalization, performed via a grafting-to method, was monitored using TGA, IR and TEM measurements. The NRs were very soluble in organic solvents after functionalization. Afterwards, the liquid crystalline (LC) behavior was investigated. During solvent evaporation, birefringent domains were formed. The self-assembly into lyotropic LC structures could be observed…

chemistry.chemical_classificationMaterials scienceNanoparticle02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistryChemical engineeringPhase (matter)LyotropicMaterials ChemistryCopolymerSurface modificationOrganic chemistryReversible addition−fragmentation chain-transfer polymerizationNanorod0210 nano-technologyJournal of Materials Chemistry C
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Direct Surface Relief Formation in Polymer Films

2013

Due to active development of nanoelectronics, the studies of methods of nanorelief surface formation in different materials, in particular polymers are very important. Organic polymer films in consequence of their dielectric and optical properties have been used as basis of these devices. In this paper, the possibility of UV optical record and electron beam lithography in different type of polymeric films was studied. Mechanisms of molecular structure changes: photoisomerization, destruction, cross-linking and oxidation have been discussed. The results of UV illumination of polyurethanes, polyacrylates, and some block-copolymers were described. The element analysis of polybutadiene block co…

chemistry.chemical_classificationMaterials sciencePhotoisomerizationbusiness.industryMechanical EngineeringPolymerDielectricPolybutadieneOpticschemistryNanoelectronicsMechanics of MaterialsCopolymerOptoelectronicsMoleculeGeneral Materials SciencebusinessElectron-beam lithographyKey Engineering Materials
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