Search results for "COPOLYMERS"

showing 10 items of 87 documents

Dynamic Self-Consistent Field Approach for Studying Kinetic Processes in Multiblock Copolymer Melts

2020

The self-consistent field theory is a popular and highly successful theoretical framework for studying equilibrium (co)polymer systems at the mesoscopic level. Dynamic density functionals allow one to use this framework for studying dynamical processes in the diffusive, non-inertial regime. The central quantity in these approaches is the mobility function, which describes the effect of chain connectivity on the nonlocal response of monomers to thermodynamic driving fields. In a recent study [Mantha et al, Macromolecules 53, 3409 (2020)], we have developed a method to systematically construct mobility functions from reference fine-grained simulations. Here we focus on melts of linear chains …

Chemical Physics (physics.chem-ph)Physicsordering kineticsMesoscopic physicsPolymers and PlasticsField (physics)Thermodynamic equilibriumDynamic structure factorFOS: Physical sciencesNon-equilibrium thermodynamicsContext (language use)General ChemistryCondensed Matter - Soft Condensed MatterDynamic densityArticlelcsh:QD241-441lcsh:Organic chemistrydynamic density functional theoryPhysics - Chemical Physicstwo-length scale copolymerssingle chain structure factorSoft Condensed Matter (cond-mat.soft)Density functional theoryStatistical physicsmultiblock copolymersPolymers
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Amphiphilic poly(hydroxyethylaspartamide) derivative-based micelles as drug delivery systems for ferulic acid

2008

Self-assembling micelles, potentially useful as drug delivery systems for ferulic acid (FA), were obtained in aqueous media from amphiphilic alpha,beta-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA) copolymers bearing at the polyamino acidic backbone both poly(ethyleneglycol) (2000 or 5000 Da) and hexadecylamine (C(16)) moieties, at a concentration of 7 x 10(- 3) and 4 x 10(- 3) g/l, respectively, with nanometre size and negative zeta potential. These micelles were able to entrap FA and to release it in a prolonged way in phosphate buffer solution at pH 7.4 and human plasma. These systems were also stable in storage conditions and have no cytotoxic effects on Caco-2, 16 HBE, HuDe and K562 cel…

Coumaric AcidsAction PotentialsPharmaceutical ScienceBuffersCoumaric acidMicelleFerulic acidMicechemistry.chemical_compoundDrug Delivery SystemsPhagocytosisamphiphilic copolymers micelles ferulic acidPolymer chemistryAmphiphileZeta potentialCopolymerAnimalsHumansTechnology PharmaceuticalOrganic chemistryMicellespolymeric micellesFluorescent DyesAmphiphilic copolymersalphabeta-poly(N-2-hydroxyethyl)-DL-aspartamidePlant ExtractsRhodaminesMacrophagesHydrogen-Ion ConcentrationchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryPEGylationCaco-2 CellsK562 CellsPeptidesRhodamine B baseferulic acidJournal of Drug Targeting
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From an epoxide monomer toolkit to functional PEG copolymers with adjustable LCST behavior.

2011

The lower critical solution temperature (LCST) behavior of novel poly(ethylene glycol) (PEG)-based copolymers bearing multiple functional groups, obtained by anionic ring-opening (co)polymerization (AROP), has been investigated. Variable comonomer ratios of ethylene oxide (EO) and the corresponding oxiranes isopropylidene glyceryl glycidyl ether (IGG), ethoxyl vinyl glycidyl ether (EVGE), allyl glycidyl ether (AGE), or N,N-dibenzyl amino glycidyl (DBAG), particularly designed to implement functional groups at the PEG backbone, were found to influence the LCST behavior. Sharp transitions from translucent to opaque solutions, comparable to other well-established stimuli-responsive polymers, w…

Ethylene OxideMaterials scienceHot TemperaturePolymers and PlasticsPolymersAllyl glycidyl etherpolyethersEpoxideLower critical solution temperaturePolymerizationPolyethylene Glycolschemistry.chemical_compoundPolymer chemistrycopolymersMaterials ChemistryCopolymerPoly(Ethylene Glycol) CopolymersSide-ChainsAqueous-SolutionEthylene oxideComonomerstimuli-sensitiveOrganic ChemistryPegchemistryPolymerizationGlycidolLcstEthylene glycolHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Polystyrene nanoparticles in the presence of (ethylene oxide)13(propylene oxide)30(ethylene oxide)13, N,N-dimethyloctylamine-N-oxide and their mixtur…

2008

Polystyrene nanoparticles were synthesized by emulsion polymerization of styrene. They were functionalized using the conventional surfactant N,N-dimethyloctylamine-N-oxide (ODAO), the tri-block copolymer (ethylene oxide)13(propylene oxide)30(ethylene oxide)13 (L64) and their mixtures. To this purpose, dynamic light scattering and calorimetric experiments were carried out and provided information consistent to each other. The L64 adsorption is Langmuir-type in the copolymer dilute regime and generates complex structures at larger concentrations. In the region where ODAO is in the unimeric state, the adsorption process is cooperative leading to hemi-micelle formation at the polystyrene nanopa…

Ethylene OxideMaterials scienceLightSurface PropertiesOxideGeneral Physics and AstronomyEmulsion polymerizationCalorimetryTRIBLOCK COPOLYMERSStyrenechemistry.chemical_compoundDynamic light scatteringAQUEOUS-SOLUTIONSPolymer chemistryCopolymerScattering RadiationPropylene oxideSURFACTANTSPhysical and Theoretical ChemistryStyreneEthylene oxideLAPONITE CLAYWaterOxidesOctanesHEAT-CAPACITIESSolutionsBLOCK-COPOLYMERSLATEXchemistryChemical engineeringNanoparticlesPolystyrenesMASS-ACTION MODELTHERMODYNAMIC PROPERTIESAdsorptionPolystyrenePhys. Chem. Chem. Phys.
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Studies on the microstructure of ethylene/1-hexene copolymers prepared over heterogeneous Ziegler - Natta catalysts

2000

Three MgCl 2(THF) 2-supported, AlEt 2Cl-activated VOCl 3, VCl 4 and TiCl 4 Ziegler - Natta catalysts were used to copolymerize ethylene with 1-hexene in the presence of hydrogen to prepare low-M well-soluble copolymers that could be analyzed by 13C-NMR. The spectra (Fig. 1) showed resonance signals due to ethylene and 1-hexene units in positions unaffected by catalyst type and with intensities related to the degree of comonomer incorporation into the copolymer. The triad sequence distribution and comonomer reactivity ratios (r) were calculated by the Randall method [11] and Bernoulli statistics based on the known copolymer composition. The latter appeared to be the more valid in predicting …

EthyleneMaterials sciencePolymers and PlasticsbiologyGeneral Chemical EngineeringmicrostructureNattaethylene/1-hexene copolymersbiology.organism_classificationMicrostructurereactivity ciefficientsCatalysis1-Hexenechemistry.chemical_compoundchemistryMgCl2(THF)2-supported V and Ti catalystsMaterials ChemistryCopolymerOrganic chemistryPolimery
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Titanium and vanadium catalysts with oxazoline ligands for ethylene-norbornene (co)polymerization

2018

A series of catalysts, (Py-ox)TiCl4, (Py-box)TiCl4, (Py-ox)VCl3, (Py-box)VCl3, SIL/(Py-ox)VCl3, SIL/(Py-box)VCl3, with 2-(1,3-oxazolin-2-yl)pyridine (Py-ox) and 2,6-bis(1,3-oxazolin-2-yl)pyridine (Py-box) ligands, silica support modified by 1-[3-(triethoxysilyl)propyl]pyridinium ethylchloroaluminate ionic liquid (SIL), activated by AlEt2Cl, AlEtCl2, and methylaluminoxane (MMAO) were studied in ethylene polymerization and ethylene-norbornene copolymerization. Single-crystal X-ray diffraction is given for both Py-ox and Py-box. The complexation was confirmed by NMR and ESI-MS methods. All complexes were found to be active in ethylene polymerization with better performance of the vanadium cata…

EthylenePolymers and Plastics010405 organic chemistryOrganic ChemistryMethylaluminoxaneGeneral Physics and AstronomynorbornenePolyethyleneoxazoline ligands010402 general chemistry01 natural sciences0104 chemical sciencesIonic liquidschemistry.chemical_compoundchemistryPolymerizationorganometallic catalystsPolymer chemistryPyridineMaterials ChemistryCopolymercopolymersethylenePyridiniumNorborneneEuropean Polymer Journal
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“Functional Poly(ethylene glycol)”: PEG-Based Random Copolymers with 1,2-Diol Side Chains and Terminal Amino Functionality

2010

A series of poly(ethylene glycol-co-isopropylidene glyceryl glycidyl ether) (P(EO-co-IGG)) random copolymers with different fractions of 1,2-isopropylidene glyceryl glycidyl ether (IGG) units was synthesized. After acidic hydrolysis a new type of "functional PEGs", namely poly(ethylene glycol-co-glyceryl glycerol) (P(EO-co-GG)) was obtained. Using an initiator that releases a terminal amino moiety after deprotection, functional end groups with orthogonal reactivity to the in-chain groups were obtained. All polymers showed narrow molecular weight distributions (1.07-1.19), and control of the molecular weights was achieved in the range 5000-30 000 g/mol. Random incorporation of both comonomer…

EthylenePolymers and PlasticsPolyglycerolDiolHigh-Loading SupportPolymerizationInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerSide chainMoietychemistry.chemical_classificationReagentsTelechelic polymerOxide)Organic ChemistryPolymerSoluble PolymersRecoverable CatalystschemistryPolymerizationGlycidolBlock-CopolymersDerivativesMacromolecules
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Homopolymerization of styrenic monomers and their copolymerization with ethylene using group 4 non‐metallocene catalysts

2020

Homopolymerization of styrenic monomers (St, p ‐Me‐St, p ‐t Bu‐St, p ‐t BuO‐St) and their copolymerization with ethylene, with the use of [( t Bu2O2NN′)ZrCl]2(μ‐O) (1 ) and ( t Bu2O2NN′)TiCl2 (2 ), where t Bu2O2NN′ = Me2N(CH2)2N(CH2‐2‐O−‐3,5‐t Bu2‐C6H2)2, is explored in the presence of MMAO and (i Bu)3Al/Ph3CB(C6F5)4. The ethylene/styrenic monomers copolymerization with 1 /MMAO produces exclusively copolymers with high activity and good comonomer incorporation whereas the other catalytic systems yield mixtures of copolymers and homopolymers. The use of p ‐alkyl styrene derivatives instead of styrene raises the catalytic activity, comonomer incorporation and molecular weights of the copolyme…

EthylenePolymers and Plasticsstructure–property relationshipsGeneral ChemistrypolystyrenecatalystsSurfaces Coatings and FilmsCatalysischemistry.chemical_compoundMonomerchemistryGroup (periodic table)Polymer chemistryMaterials ChemistryCopolymercopolymersPolystyreneMetalloceneJournal of Applied Polymer Science
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Polyaspartamide-g-Polylactide graft cpolymers able to form nanoparticles obtained by a novel synthetic strategy.

2009

GRAFT COPOLYMERS POLYMERIC NANOPARTICLES POLY(LACTIC ACID)Settore CHIM/09 - Farmaceutico Tecnologico Applicativo
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Squaric Acid Mediated Synthesis and Biological Activity of a Library of Linear and Hyperbranched Poly(Glycerol)-Protein Conjugates

2012

Polymer-protein conjugates generated from side chain functional synthetic polymers are attractive because they can be easily further modified with, for example, labeling groups or targeting ligands. The residue specific modification of proteins with side chain functional synthetic polymers using the traditional coupling strategies may be compromised due to the nonorthogonality of the side-chain and chain-end functional groups of the synthetic polymer, which may lead to side reactions. This study explores the feasibility of the squaric acid diethyl ester mediated coupling as an amine selective, hydroxyl tolerant, and hydrolysis insensitive route for the preparation of side-chain functional, …

GlycerolModels MolecularCovalent AttachmentPolymers and PlasticsPolymersBioengineeringSquaric acidImmunological PropertiesLigandsSmall Molecule LibrariesBiomaterialsHydrolysischemistry.chemical_compoundResidue (chemistry)Thiazolidine-2-ThioneMaterials ChemistrySide chainCopolymerOrganic chemistryBovine Serum-Albuminchemistry.chemical_classificationPoly(Ethylene Glycol)Molecular StructureCopolymersPolymer StructureSerum Albumin BovinePolymerPolyethylene-GlycolMolecular WeightPolyglycerolschemistryMuramidaseAmine gas treatingFunctional polymersCyclobutanesDerivatives
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