Search results for "surface"

showing 10 items of 9345 documents

Linear–dendritic block copolymers: The state of the art and exciting perspectives

2011

Concurrent with the rapid development of both dendrimers and hyperbranched polymers, a novel class of block copolymer architectures has emerged from the combination of these dendritic architectures with linear chains, the “linear–dendritic block copolymers” (LDBCs). This review gives a comprehensive summary of the state of the art in this rapidly developing field from pioneering early work to promising recent approaches.The different strategies leading to these hybrid architectures with either perfect dendrimer/dendron building blocks or imperfect, yet more conveniently accessible hyperbranched segments, are reviewed and compared. The consequences of the unusual polymer topology for supramo…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryHyperbranched polymersSupramolecular chemistrySolid-stateNanotechnologySurfaces and InterfacesPolymerchemistryDendrimerPolymer chemistryMaterials ChemistryCeramics and CompositesCopolymerState (computer science)Topology (chemistry)Progress in Polymer Science
researchProduct

Self-organization of hydrophobized polyzwitterions

1992

Abstract Several series of copolymers of different geometry were synthesized from zwitterionic surfactant monomers and polar non-ionic comonomers. Bulk properties were investigated by d.s.c. and X-ray scattering. The copolymers were amorphous, but exhibited superstructures up to high commonomer contents. Solubility of the copolymers was determined as a function of geometry and composition. From the results, a main chain spacer model has been derived. All water-soluble copolymers exhibited characteristic features of classical polysoaps, as shown by surface tension measurements and by solubilization of pyrene. But gradual differences depending on the polymer geometry were observed for the sol…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerMicelleSurface tensionchemistry.chemical_compoundMonomerChemical engineeringchemistryPulmonary surfactantPolymer chemistryMaterials ChemistryCopolymerPyreneSolubilityPolymer
researchProduct

Liquid Crystals from Polymer-Functionalized TiO2 Nanorod Mesogens

2008

In this work, we functionalized TiO2 nanorods with dopamine-functionalized diblock copolymers. After functionalization, they are well dispersible in organic solvents. Light scattering proves that t...

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationChain transferPolymerLight scatteringInorganic ChemistrychemistryLiquid crystalPolymer chemistryMaterials ChemistryCopolymerSurface modificationNanorodMacromolecules
researchProduct

Synthesis of Functional Inorganic−Organic Hybrid Polymers Based on Poly(silsesquioxanes) and Their Thin Film Properties

2008

New stable and adherent coating materials have been synthesized on the basis of inorganic/organic hybrid polymers. As the inorganic part, different poly(silsesquioxanes) (PSSQ) have been functionalized to act as polymeric chain transfer agents (CTAs) for a reversible addition fragmentation chain transfer polymerization, thereby determining the starting point of a controlled radical polymerization of vinyl-type monomers. Using two different CTAs acrylates, we have successfully polymerized methacrylates and styrene under RAFT polymerization conditions. Different monomers were copolymerized in such an organic block to incorporate multiple functionalities. The variation of the block ratios and …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agricultureChain transfermacromolecular substancesPolymerMethacrylateInorganic ChemistrySurface coatingPolymerizationchemistryPolymer chemistryMaterials ChemistrySurface modificationReversible addition−fragmentation chain-transfer polymerizationMacromolecules
researchProduct

Analysis of the intensities of the longitudinal acoustic vibrations inn-alkanes and polyethylene

1980

Simple theoretical considerations indicate, that the integral intensity of the „longitudinal acoustic modes” (LAM) in the Raman spectrum ofn-alkanes should be independent of the chain length. The experiment in fact confirms this expectation. Using this property it becomes possible for polyethylene samples, to derive from the measured LAM-intensity the mass fraction of all-turns sequences contributing to this band. For solution crystallized samples this fraction coincides with the crystallinity, whereas in melt crystallized samples it generally turns out as smaller. The observed difference is likely to be due to the occurrence of local conformational defects (kinks, chain torsions) which int…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPolymerPolyethyleneMolecular physicsVibrationCrystallinitychemistry.chemical_compoundCrystallographysymbols.namesakeColloid and Surface ChemistrychemistryMaterials ChemistrysymbolsCrystallitePhysical and Theoretical ChemistryRaman spectroscopyMass fractionIntensity (heat transfer)Colloid and Polymer Science
researchProduct

Rheological properties of progesterone microemulsions: Influence of xanthan and chitosan biopolymer concentration

2008

In this preformulations study, rheological properties of microemulsions with progesterone (1%) were studied to analyze the effect of xanthan and chitosan at different concentrations (0.5–3%). Steady shear and oscillatory rheological properties were analyzed using a controlled stress rheometer. Steady shear data were satisfactorily adjusted to the Carreau model. For all preparations, shear-thinning behavior was observed. Zero shear viscosity (η0) increased with the biopolymer concentration. The results from dynamic experiments showed the behavior of all preparations with xanthan gum and those of chitosan to be characteristic of weak gels and liquid-like solutions, respectively. The correlati…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsRheometerGeneral ChemistryPolymerengineering.materialViscoelasticitySurfaces Coatings and FilmsChitosanchemistry.chemical_compoundchemistryChemical engineeringRheologyPolymer chemistryMaterials ChemistryengineeringmedicineMicroemulsionBiopolymerXanthan gummedicine.drugJournal of Applied Polymer Science
researchProduct

Small angle X-ray scattering from amorphous polymers arising from heterogeneities

1973

The small angle X-ray scattering of glassy polymers (PET, PC, PVC, PMMA) and of polymer melts (PE) was studied. The dependence of the intensity scattered at small angles on the sample treatment suggests that neither the inherent structure of the pure polymer phase nor microholes are the origin of the scattering. In agreement with all experimental facts the scattering can be attributed to foreign particles such as for instance stabilizers in the polymer matrix. The consequence of this result is discussed with respect to the nodular structure of the amorphous phase and with respect to structural models of the amorphous phase. The nodular structure is not related to regions of different densit…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsScatteringSmall-angle X-ray scatteringPolymerAmorphous solidCondensed Matter::Soft Condensed MatterMatrix (mathematics)CrystallographyColloid and Surface ChemistrychemistryChemical physicsPhase (matter)Materials ChemistryPhysical and Theoretical ChemistryWide-angle X-ray scatteringIntensity (heat transfer)Kolloid-Zeitschrift und Zeitschrift für Polymere
researchProduct

Morphology, rheology, and mechanical properties of a new nanobiocomposite

2015

Nanobiocomposites are a new class of biodegradable polymer materials with an ultrafine phase dispersion of the order of a few nanometers in a biodegradable polymer matrix that shows very interesting properties often very different from those of conventional filled polymers. In this work the morphology and the rheological and mechanical properties of a new nanobiocomposite made of a biodegradable copolyester based blend with an organomodified montmorillonite have been investigated to evaluate its possible use in several applications. SAXS diffractograms and TEM micrographs show that the in both the adopted processing conditions an hybrid intercalated/exfoliated morphology is observed. Rheolo…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSmall-angle X-ray scatteringGeneral ChemistryPolymerBiomaterialBiodegradable polymerCopolyesterSurfaces Coatings and Filmschemistry.chemical_compoundMontmorillonitechemistryRheologyPhase (matter)Properties and characterizationMaterials ChemistryNanostructured polymerComposite materialRheologyElastic modulusJournal of Applied Polymer Science
researchProduct

Dynamics of phase separation and critical phenomena in polymer mixtures

1987

The phenomenological mean-field theory for statics and dynamics of polymer mixtures is described, generalizing the approaches of Flory-Huggins, Cahn-Hilliard and de Gennes. Predictions are made for critical behavior, spinodal decomposition and homogeneous nucleation. The validity of the mean-field approximations is discussed with Ginzburg criteria. The results of the theory are compared to computer simulations and recent experiments.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSpinodal decompositionCritical phenomenaNucleationThermodynamicsPolymerCondensed Matter::Soft Condensed MatterColloid and Surface ChemistrychemistryCritical point (thermodynamics)HomogeneousMaterials ChemistryStatistical physicsPhysical and Theoretical ChemistryStaticsColloid and Polymer Science
researchProduct

Master curves of viscoelastic behavior in the plastic region of a solid polymer

1977

Stress relaxation and creep tests following strain ramps were made on Mylar, both above and below the yield stress. The ramp velocity was varied over a 40-fold range. All data exhibit nonlinear viscoelastic behavior. However, those obtained above the yield point, i.e., in the plastic region, could be reduced to single master curves for both the creep and the relaxation tests by means of a simple time shift factor. This factor is inversely proportional to the strain rate existing just prior to the test.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsStrain (chemistry)General ChemistryPolymerStrain rateViscoelasticitySurfaces Coatings and FilmsNonlinear systemchemistryCreepMaterials ChemistryStress relaxationForensic engineeringRelaxation (physics)Composite materialJournal of Applied Polymer Science
researchProduct