Search results for "Polymers"

showing 10 items of 3567 documents

Loading of polymer nanocarriers: Factors, mechanisms and applications

2014

Abstract The progress in synthetic polymer chemistry has allowed the precise design of hybrid and multifunctional colloidal particles, which differ in type, size and shape, thus enhancing their possible applications as target-oriented carriers of low and high molar mass active species. This survey discusses the basic principles and factors, associated with the process of loading of polymeric nanoparticles. For the purpose of this review, the polymeric nano-carriers are divided into five most studied types: micelles, nanogels, capsules (incl. vesicles), dendrimers, and hybrid nanoparticles with porous cores. Factors influencing the loading are described and their importance discussed. An imp…

chemistry.chemical_classificationMolar massMaterials sciencePolymers and PlasticsVesicleOrganic ChemistryNanoparticleNanotechnologySurfaces and InterfacesPolymerPolymeric nanoparticlesMicellechemistryDendrimerMaterials ChemistryCeramics and CompositesNanocarriersProgress in Polymer Science
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Fluorescence Correlation Spectroscopy in Dilute Polymer Solutions: Effects of Molar Mass Dispersity and the Type of Fluorescent Labeling

2015

Fluorescence correlation spectroscopy (FCS) has become an important tool in polymer science. Among various other applications the method is often applied to measure the hydrodynamic radius and the degree of fluorescent labeling of polymers in dilute solutions. Here we show that such measurements can be strongly affected by the molar mass dispersity of the studied polymers and the way of labeling. As model systems we used polystyrene and poly(methyl methacrylate) synthesized by atom transfer radical polymerization or free-radical polymerization. Thus, the polymers were either end-labeled bearing one fluorophore per chain or side-labeled with a number of fluorophores per chain proportional to…

chemistry.chemical_classificationMolar massPolymers and PlasticsAtom-transfer radical-polymerizationOrganic ChemistryDispersityAnalytical chemistryFluorescence correlation spectroscopyPolymerDegree of polymerizationInorganic ChemistrychemistryPolymerizationMaterials ChemistryMolar mass distributionACS Macro Letters
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1996

An iterative, approximative procedure is presented, to calibrate the determination of molar masses of polymers with gel-permeation chromatography, additionally using viscometry, and transformations, according to Benoit's concept of universal calibration, even if only polymers with broad molar mass distribution are available. The calculated (intermediate) values of the average molar masses from each step of iteration converge to final values. With at least two fractions of the polymers to be analyzed, and with measured intrinsic viscosities of the fractions, a calibration curve of gel-permeation chromatography and Mark-Houwink's constants can be determined. Assumptions for the use of the cal…

chemistry.chemical_classificationMolar massPolymers and PlasticsCalibration curveChemistryOrganic ChemistryAnalytical chemistryViscometerPolymerCondensed Matter PhysicsGel permeation chromatographyOsmometerMaterials ChemistryCalibrationMolar mass distributionPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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1995

Supramolecular structures based on 4-(3,5-dioxo-1,2,4-triazolidin-4-yl) benzoic acid (U4A) units act as effective junction zones in functionalized polybutadienes, resulting in the formation of thermoplastic elastomers. The dynamics on a molecular scale of the phenyl rings have been probed by 2H-NMR. In the polymeric system, there are three spatially separated environments, which are reflected in the mobility of the polar units. Phenyl rings which are incorporated in the structures are either rigid or undergo 180° phenyl flips. The small fraction of free functional groups move isotropically and their mobility is coupled to the dynamics of the polybutadiene matrix. In two model compounds, whe…

chemistry.chemical_classificationMolar massPolymers and PlasticsChemistryHydrogen bondGeneral Chemical EngineeringSupramolecular chemistryActivation energyPolymerCrystallographyPolybutadienePolymer chemistryMoleculeThermoplastic elastomerActa Polymerica
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Continuous polymer fractionation of polysaccharides using highly substituted trimethylsilylcellulose

1998

Trimethylsilylcellulose (TMSC) was prepared from commercial cellulose with a mixture of hexamethyldisilazane and chlorotrimethylsilane in the solvent system N,N-dimethylacetamide/lithium chloride. The soluble, highly silylated polymer (degree of substitution, DS 2.9) had a molar mass M, of 500 kg/mol and a molecular non-uniformity U = (M w /M n )- 1 of 2.9. In order to investigate the principal suitability of a continuous polymer fractionation for polysaccharides like cellulose derivatives and to obtain TMSC with different molecular weights and lower non-uniformity TMSC was fractionated by means of CPF (Continuous Polymer Fractionation), well-established in the field of synthetic polymers. …

chemistry.chemical_classificationMolar massPolymers and PlasticsChemistryOrganic ChemistryFractionationPolymerCondensed Matter PhysicsDimethylacetamideSolventGel permeation chromatographychemistry.chemical_compoundPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryPolymer fractionationTetrahydrofuranMacromolecular Chemistry and Physics
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Cellulose/Water:  Liquid/Gas and Liquid/Liquid Phase Equilibria and Their Consistent Modeling

2007

Liquid/liquid and liquid/gas equilibria were measured for the water/cellulose system at 80 °C using three different polymer samples. For these experiments we prepared cellulose films of approximately 20−25 μm in thickness and determined their equilibrium swelling in water. Thereafter the polymer concentration in the mixed phase was increased by means of a stepwise removal of the volatile component, and the equilibrium vapor pressures were measured using an automated combination of head space sampling and gas chromatography. Contrary to the usual behavior of polymers, the swelling of cellulose increases as its molar mass becomes larger. The Flory−Huggins interaction parameters calculated fro…

chemistry.chemical_classificationMolar massPolymers and PlasticsComponent (thermodynamics)Liquid gasAnalytical chemistryThermodynamicsBioengineeringPolymerBiomaterialschemistry.chemical_compoundchemistryPhase (matter)Materials ChemistrymedicineGas chromatographyCelluloseSwellingmedicine.symptomBiomacromolecules
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Viscosity-molecular weight relationship for cellulose solutions in either NMMO monohydrate or cuen

2010

The intrinsic viscosities, [η], of nine cellulose samples, with molar masses from 50 × 103 to 1 390 × 103 were determined in the solvents NMMO*H2O (N-methyl morpholin N-oxide hydrate) at 80°C and in cuen (copper II-ethlenediamine) at 25°C. The evaluation of these results with respect to the Kuhn–Mark–Houwink relations shows that the data for NMMO*H2O fall on the usual straight line in the double logarithmic plots only for M ≤ 158 103; the corresponding [η]/M relation reads log ([η]/mL g−1) = –1.465 + 0.735 log M. Beyond that molar mass [η] remains almost constant up to M ≈ 106 and increases again thereafter. In contrast to NMMO*H2O the cellulose solutions in cuen behave normal and the Kuhn–…

chemistry.chemical_classificationMolar massPolymers and PlasticsIntrinsic viscosityAnalytical chemistrychemistry.chemical_elementGeneral ChemistryPolymerCopperSurfaces Coatings and Filmschemistry.chemical_compoundViscositychemistryPolymer chemistryMaterials ChemistryCelluloseta216Hydrateta215Journal of Applied Polymer Science
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Molecular characterization of α , β -poly(asparthylhydrazide) a new synthetic polymer for biomedical applications

1999

Abstract α , β -Poly(asparthylhydrazide) (PAHy) is a new synthetic polymer that exhibits interesting properties and is a candidate for biomedical applications. In this article the characterization of PAHy polymer by multi-angle laser light scattering (MALS) and single-capillary viscometer (SCV) detectors on-line to a size exclusion chromatography (SEC) system is reported. The SEC–MALS–SCV system furnishes exhaustive and consistent characterization of the PAHy polymer. Further, it is possible to characterize the PAHy polymer through conventional SEC and universal calibration. The universal calibration method gives intrinsic viscosity and dispersity very close to those measured by the absolut…

chemistry.chemical_classificationMolar massPolymers and PlasticsIntrinsic viscosityOrganic ChemistryDispersitySize-exclusion chromatographyViscometerPolymerCharacterization (materials science)chemistryPolymer chemistryMaterials ChemistryRadius of gyrationPhysical chemistryPolymer
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Entanglement Transition in Hyperbranched Polyether-Polyols

2010

Are hyperbranched polymers capable of forming entanglements? This is the central issue of this contribution. Hyperbranched polyglycerol (hbPG) samples with different molecular weights (600-106 000 g · mol(-1) ), narrow polydispersities (1.2-1.8) and high degrees of branching (≈0.6) were prepared by anionic ring-opening polymerization. The viscoelastic properties of these polymers with respect to molecular architecture and molar mass were investigated. At low molecular weights "classical" scaling behavior between zero shear viscosity and molecular weight can be observed, whereas between 3 000 and 10 000 g · mol(-1) a plateau-like area is found. The results indicate entanglement dynamics when…

chemistry.chemical_classificationMolar massPolymers and PlasticsMolecular massOrganic ChemistryThermodynamicsPolymerBranching (polymer chemistry)ViscoelasticitychemistryRheologyPolymerizationPolymer chemistryMaterials ChemistryScalingMacromolecular Rapid Communications
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Viscometry of polyelectrolyte solutions: Star-like versus linear poly[[2-(methacryloyloxy)ethyl] trimethylammonium iodide] and specific salt effects

2017

Abstract The intrinsic viscosities, [η], of the 3-arm star polyelectrolyte in pure water are for a given molar mass considerably lower than for the linear product because of the higher monomer concentration and charge density in isolated coils. These effects are much more pronounced than in the case of uncharged macromolecules. Extra salt (NaCl, NaI, CaCl2) reduces the solution viscosities of the 3-arm star polymer less than of the linear product. The transition of [η] from the value in pure water to the minimum saturation value at high salt concentrations follows a Boltzmann sigmoid. In saline solvents the changes of the viscosities with rising polymer concentration depend strongly on the …

chemistry.chemical_classificationMolar massPolymers and PlasticsOrganic ChemistryIodideGeneral Physics and AstronomyThermodynamicsViscometerSalt (chemistry)Charge density02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPolyelectrolyte0104 chemical scienceschemistry.chemical_compoundMonomerchemistryMaterials ChemistryOrganic chemistry0210 nano-technologyEuropean Polymer Journal
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