Search results for "Copolymer"

showing 10 items of 1003 documents

Effect of Core-Crosslinking on Protein Corona Formation on Polymeric Micelles.

2021

Most nanomaterials acquire a protein corona upon contact with biological fluids. The magnitude of this effect is strongly dependent both on surface and structure of the nanoparticle. To define the contribution of the internal nanoparticle structure, protein corona formation of block copolymer micelles with poly(N-2-hydroxypropylmethacrylamide) (pHPMA) as hydrophilic shell, which are crosslinked-or not-in the hydrophobic core is comparatively analyzed. Both types of micelles are incubated with human blood plasma and separated by asymmetrical flow field-flow fractionation (AF4). Their size is determined by dynamic light scattering and proteins within the micellar fraction are characterized by…

Polymers and PlasticsChemical PhenomenaLightPolymersNanoparticleBioengineeringProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesMicelleMass SpectrometryPolyethylene GlycolsBiomaterialsCorona (optical phenomenon)PlasmaDynamic light scatteringMaterials ChemistryCopolymerHumansScattering RadiationChromatography High Pressure LiquidMicellesGel electrophoresisChemistry021001 nanoscience & nanotechnologyBlood proteins0104 chemical sciencesNanostructuresCross-Linking ReagentsBiophysicsProtein CoronaAdsorption0210 nano-technologyHydrophobic and Hydrophilic InteractionsBiotechnologyMacromolecular bioscience
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Thermal stability of poly(styrene-b-methyl methacrylate) and poly(styrene-b-ethylene-co-1-butene-b-methyl methacrylate)

1993

The thermal stability of poly(styrene-b-methyl methacrylate) diblock copolymers (= P(S-b-MMA)) and poly(styrene-b-ethylene-co-1-butene-b-methyl methacrylate) triblock copolymers (=P(S-b-EB-b-MMA)) was investigated. Well-defined high molecular weight block copolymers with narrow molecular weight distribution (MWD) were molded at different temperatures in vacuum and the alteration of the MWD was sensitively monitored by gel permeation chromatography (GPC). Up to 240°C P(S-b-MMA) shows almost no broadening of the MWD. At higher temperatures low molecular weight polystyrene-rich portions are formed. The number average molecular weight (Mn) is strongly reduced. P(S-b-EB-b-MMA) triblock copolymer…

Polymers and PlasticsChemistry1-ButeneGeneral ChemistryCondensed Matter PhysicsMethacrylateStyreneGel permeation chromatographychemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerMolar mass distributionThermal stabilityMethyl methacrylatePolymer Bulletin
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New hyaluronic acid based brush copolymers synthesized by atom transfer radical polymerization.

2013

Abstract In this work, an efficient method for the synthesis of hyaluronic acid based brush copolymers using atom transfer radical polymerization (ATRP) has been reported. At first, two different hyaluronic acid (HA) based macroinitiators have been prepared and then they have been used for the polymerization via ATRP of hydrophilic or hydrophobic molecules carrying vinyl portions. In particular, by linking 2-bromo-2-methylpropionic acid (BMP) to the primary hydroxyl groups of tetrabutyl ammonium salt of HA (HA–TBA) or to amino groups of the ethylenediamino derivative of HA–TBA (HA–TBA–EDA), two macroinitiators (HA–TBA–BMP and HA–TBA–EDA–BMP) have been obtained. Then they have been used for …

Polymers and PlasticsChemistryAtom-transfer radical-polymerizationPolymersOrganic ChemistrySize-exclusion chromatographyBiocompatible MaterialsChemistry Techniques SyntheticMethacrylateEthylenediaminesPolymerizationMolecular Weightchemistry.chemical_compoundLiving free-radical polymerizationPolymerizationPolymer chemistryMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationHyaluronic AcidPropionatesEthylene glycolCarbohydrate polymers
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Polymerization of styrene

1979

Polymers and PlasticsChemistryChain transferGeneral ChemistryCondensed Matter PhysicsChain-growth polymerizationAnionic addition polymerizationPolymerizationPolymer chemistryMaterials ChemistryCopolymerLiving polymerizationReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationPolymer Bulletin
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Copolymerization of Isoprene with p-Alkylstyrene Monomers: Disparate Reactivity Ratios and the Shape of the Gradient

2019

The statistical copolymerization of isoprene with p-ethyl- (p-ES), p-isopropyl- (p-iPS), and p-tert-butylstyrene (p-tBS) initiated by sec-butyllithium in cyclohexane was investigated with respect to kinetics, reactivity ratios, and formation of tapered block copolymers with pronounced monomer gradient. An efficient synthetic route to the monomers was developed on a multigram scale, relying on the precipitation of the side-product triphenylphosphine oxide at low temperature. The copolymerization kinetics and resulting molecular weight distributions were analyzed. The dispersity, Đ, of the copolymers depends on the p-alkyl substituent, the the degree of polymerization Pn and the comonomer mol…

Polymers and PlasticsChemistryComonomerOrganic ChemistryDispersity02 engineering and technologyDegree of polymerization010402 general chemistry021001 nanoscience & nanotechnologyMole fraction01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundMonomerPolymer chemistryMaterials ChemistryCopolymerReactivity (chemistry)0210 nano-technologyIsopreneMacromolecules
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Hyperbranched Polyols via Copolymerization of 1,2-Butylene Oxide and Glycidol: Comparison of Batch Synthesis and Slow Monomer Addition

2015

Hyperbranched poly(butylene oxide) polyols have been synthesized by multibranching anionic ring-opening copolymerization of 1,2-butylene oxide and glycidol. Systematic variation of the composition from 24 to 74% glycidol content resulted in a series of moderately distributed copolymers (Đ = 1.41–1.65, SEC), albeit with limited molecular weights in the solvent-free batch process in the range of 900–1300 g mol–1 (apparent Mn determined by SEC with PEG standards). In situ monitoring of the copolymerization kinetics by 1H NMR showed a pronounced compositional drift with respect to the monomer feed, indicating a strongly tapered microstructure caused by the higher reactivity of glycidol. In the …

Polymers and PlasticsChemistryComonomerOrganic ChemistryGlycidolOxide02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundMonomerPolymer chemistryPEG ratioMaterials ChemistryCopolymerReactivity (chemistry)0210 nano-technologyGlass transitionMacromolecules
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Blends of polyamide 6 and bisphenol-A polycarbonate. Effects of interchange reactions on morphology and mechanical properties

1992

Blends of polyamide 6 (PA6) and polycarbonate (PC) were prepared in a Brabender mixer, at 240°C, applying long mixing time, for 45 min. It was observed that the morphology and the mechanical properties tend to resemble those of a homogeneous material as the mixing time and PA6 concentration increase. This is attributed to chemical reactions taking place between the two homopolymers. Acidolysis, amidolysis, and aminolysis, catalyzed by the terminals and the amide groups of the polyamide, should in principle be possible. Our results indicate that the aminolysis is the main process, inducing simultaneously scission of PC chains and formation of PC-PA6 copolymer chains. The latter act as interf…

Polymers and PlasticsChemistryMixing (process engineering)General ChemistryChemical reactionSurfaces Coatings and FilmsCatalysisAminolysisPhase (matter)visual_artPolyamidePolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumCopolymerPolycarbonateJournal of Applied Polymer Science
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Racemic S ‐(ethylsulfonyl)‐ dl ‐cysteine N ‐Carboxyanhydrides Improve Chain Lengths and Monomer Conversion for β‐Sheet‐Controlled Ring‐Opening Polyme…

2020

The secondary structure formation of polypeptides not only governs folding and solution self-assembly but also affects the nucleophilic ring-opening polymerization of alpha-amino acid-N-carboxyanhydrides (NCAs). Whereby helical structures are known to enhance polymerization rates, beta-sheet-like assemblies reduce the propagation rate or may even terminate chain growth by precipitation or gelation. To overcome these unfavorable properties, racemic mixtures of NCAs can be applied. In this work, racemicS-(ethylsulfonyl)-dl-cysteine NCA is investigated for the synthesis of polypeptides, diblock and triblock copolypept(o)ides. In contrast to the polymerization of stereoregularS-(ethylsulfonyl)-…

Polymers and PlasticsChemistryOrganic ChemistryBeta sheet02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesRing-opening polymerizationPolymerization0104 chemical scienceschemistry.chemical_compoundMonomerReaction rate constantPolymerizationNucleophileYield (chemistry)Polymer chemistryMaterials ChemistryCopolymerProtein Conformation beta-StrandCysteineAmino AcidsPeptides0210 nano-technologyMacromolecular Rapid Communications
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Study of the molecular origin of the mechanical and dielectric β relaxation of methyl methacrylate/isopropenyl methyl ketone copolymers

1988

Resultats de l'etude dielectrique, mecanique et par TSC en faveur d'une combinaison d'une barriere intra- et intermoleculaire dans la relaxation beta

Polymers and PlasticsChemistryOrganic ChemistryEnthalpyDielectricActivation energyCondensed Matter PhysicsMolecular dynamicschemistry.chemical_compoundTacticityPolymer chemistryMaterials ChemistryCopolymerStress relaxationMethyl methacrylateMakromolekulare Chemie. Macromolecular Symposia
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RAFT Synthesis of Reactive Multifunctional Triblock‐Copolymers for Polyplex Formation

2021

Polymers and PlasticsChemistryOrganic ChemistryPolymer chemistryMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationRaftPhysical and Theoretical ChemistryCondensed Matter PhysicsMacromolecular Chemistry and Physics
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