Search results for "polymers"

showing 10 items of 3567 documents

Amino Functional Poly(ethylene glycol) Copolymers via Protected Amino Glycidol

2010

The synthesis of poly(ethylene glycol) (PEG) copolymers with multiple amino functionalities within the chain is described, relying on an epoxide comonomer bearing a protected amino group. N,N-dibenzyl amino glycidol (DBAG) and ethylene oxide (EO) were copolymerized via anionic polymerization, leading to well-defined polymers with varied comonomer content and low polydispersities (Mw/Mn in the range of 1.1 to 1.2). Subsequent hydrogenolysis with Pearlman’s catalyst afforded poly(ethylene glycol-co-amino glycerol)s (PEG-co-PAG) with a precisely adjusted number of randomly incorporated amino groups in the range of 2−15%. For the first time, the kinetics of an EO copolymerizations have has been…

EthylenePolymers and PlasticsEthylene oxideComonomerOrganic Chemistrytechnology industry and agricultureGlycidolEpoxideInorganic Chemistrychemistry.chemical_compoundAnionic addition polymerizationMonomerchemistryPolymer chemistryMaterials ChemistryOrganic chemistryEthylene glycolMacromolecules
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Effective copolymerization of ethylene with α,ω-alkenols and homopolymerization of α,ω-alkenols catalyzed by aminophenolate zirconium complex

2019

Abstract A zirconium complex of diamine-bis(phenolate) ligand, [(tBu2O2NN’)ZrCl]2(μ-O) where (tBu2O2NN’) = Me2N(CH2)2N(CH2–2-O−-3,5-tBu2-C6H2)2, activated with (iBu)3Al/Ph3CB(C6F5)4, was for the first time used in copolymerization of ethylene with unsaturated alcohols (CH2 = CH(CH2)nCH2OH, where n = 7, 8, 3). The hydroxyl groups of comonomers were protected with R3-xAlClx (where x = 0 or 1, R = iBu, Et). In contrast to the formerly reported catalysts, the activity of this catalyst is much higher in ethylene/alkenols copolymerization than in ethylene homopolymerization and its lifetime is long. Moreover, the copolymers with high polar comonomer contents (up to 16.4 mol%, 52.3 wt%) were produ…

EthylenePolymers and PlasticsGeneral Chemical Engineeringαchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryCatalysischemistry.chemical_compoundcoordination polymerizationω-alkenolsPolymer chemistryethyleneMaterials ChemistryCopolymerEnvironmental Chemistryfunctionalization of polymersZirconiumLigandComonomerGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryPolymerizationCoordination polymerization0210 nano-technologyReactive and Functional Polymers
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Organometallic vanadium‐based heterogeneous catalysts for ethylene polymerization. Study of the deactivation process

1998

Slurry polymerizations of ethylene over vanadium catalysts (based on VCl4 and VOCl3) and their MgCl2(THF)2-supported equivalents were studied. Unsupported vanadium catalysts were found to be unstable while the vanadium active sites deposited on the MgCl2(THF)2 complex are stable. A sharply outlined correlation was found between the concentration of vanadium(III) and catalyst productivity. The high activity and stability of the vanadium catalyst when supported on the magnesium complex is attributed to the increase of resistance to reduction of active vanadium(III) to inactive vanadium(II) by an organoaluminium co-catalyst.

EthylenePolymers and PlasticsMagnesiumOrganic ChemistryInorganic chemistryVanadiumchemistry.chemical_elementPolyethyleneCatalysischemistry.chemical_compoundchemistryEthylene polymerizationMaterials ChemistrySlurryHigh activityMacromolecular Rapid Communications
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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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The role of crystalline, mobile amorphous and rigid amorphous fractions in the performance of recycled poly (ethylene terephthalate) (PET)

2012

[EN] The action of thermo-mechanical degradation induced by mechanical recycling of poly(ethylene terephthalate) was simulated by successive injection moulding cycles. Degradation reactions provoked chain scissions and a reduction in molar mass mainly driven by the reduction of diethyleneglycol to ethylene glycol units in the flexible domain of the PET backbone, and the formation of -OH terminated species with shorter chain length. The consequent microstructural changes were quantified taking into account a three-fraction model involving crystalline, mobile amorphous (MAF) and rigid amorphous fractions (RAF). A remarkable increase of RAF, to a detriment of MAF was observed, while the percen…

EthyleneSolucions polimèriquesPolymers and PlasticsInjection mouldingDifferential scanning calorimetry (DSC)Crystalline fractionsMechanical propertiesThermo-mechanical degradationchemistry.chemical_compoundDegradationAmorphous materialsPolymer blendsMaterials ChemistryMechanical recyclingRecyclingComposite materialDiethyleneglycolPoly(ethylene terephthalate) (PET)Injection moldingMolar massMechanical featureRecycled poly(ethylene terephthalate)Microstructural changesCondensed Matter PhysicsChain scissionRigid-amorphous fractionMechanics of MaterialsMAQUINAS Y MOTORES TERMICOSPolymer blendMaterials scienceMechanical performanceViscoelasticityEthyleneDifferential scanning calorimetrySegmental dynamicsInfrared analysis (FT-IR)Degradation reactionDifferential scanning calorimetryInjection mouldingPolyethylene terephthalatesEthylene glycolTermoplàsticsCrystalline materialsShorter chainsAmorphous solidchemistryGlass-rubber relaxationProcessing cyclesEthylene glycol
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Polymeric microcontainers improve oral bioavailability of furosemide.

2016

Microcontainers with an inner diameter of 223 μm are fabricated using the polymer SU-8, and evaluated in vitro, in situ and in vivo for their application as an advanced oral drug delivery system for the poorly water soluble drug furosemide. An amorphous sodium salt of furosemide (ASSF) is filled into the microcontainers followed by applying a lid using Eudragit L100. It is possible to control the drug release in vitro, and in vitro absorption studies show that the microcontainers are not a hindrance for absorption of ASSF. In situ perfusion studies in rats are performed with ASSF-filled microcontainers coated with Eudragit and compared to a furosemide solution. The absorption rate constant …

Eudragit l100PolymersPharmaceutical ScienceAdministration OralBiological Availability02 engineering and technologyAbsorption (skin)PharmacologyMicro devices030226 pharmacology & pharmacy03 medical and health sciences0302 clinical medicineDrug Delivery SystemsPolymethacrylic AcidsIn vivoDelivery systemsFurosemideOral bioavailabilitymedicineAnimalsHumansIntestinal MucosaRats WistarIntestinal mucusChromatographyChemistryFurosemide021001 nanoscience & nanotechnologyBioavailabilityDrug LiberationMucusOral deliveryEpoxy CompoundsFemaleDelivery systemIntestinal perfusionCaco-2 Cells0210 nano-technologyOral retinoidmedicine.drugInternational journal of pharmaceutics
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Colloidal Nanoplatelet/Conducting Polymer Hybrids: Excitonic And Material Properties

2016

WOS:000370678700053 Here we present the first account of conductive polymer/colloidal nanoplatelet hybrids. For this, we developed DEH-PPV-based polymers with two different anchor groups (sulfide and amine) acting as surfactants for CdSe nanoplatelets, which are atomically flat semiconductor nanocrystals. Hybridization of the polymers with the nanoplatelets in the solution phase was observed to cause strong photoluminescence quenching in both materials. Through steady-state photoluminescence and excitation spectrum measurements, photoluminescence quenching was shown to result from dominant exciton dissociation through charge transfer at the polymer/nanoplatelet interfaces that possess a sta…

Excitation spectrumMaterials sciencePhotoluminescenceSulfideDEH-PPV-Based PolymersSulfideExcitonCdSe NanoplateletsNanotechnology02 engineering and technologySurface active agents010402 general chemistryOptoelectronic devices01 natural sciencesDissociation (chemistry)ColloidCharge transferQuenchingHybrid optoelectronic devicesPhysical and Theoretical ChemistryPhotoluminescenceSulfur compoundsAmineSemiconductor nanocrystalsConductive polymerchemistry.chemical_classificationExcited statesBuilding blockesPolymerInterface statesEmission quenching021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPolymer/Colloidal Nanoplatelet HybridsGeneral EnergyChemical engineeringchemistryExcited stateAnchorsExcitons0210 nano-technologyDissociationConductive polymerPhotoluminescence quenchingExciton dissociation
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Modelling of phase transitions and residual thermal stress of CTBN rubber modified epoxy resins during a pultrusion process

2007

Abstract The implicit finite difference and fourth order Runge-Kutta method are used both to solve the heat transfer problem in the pultrusion reaction and to calculate the temperature and conversion distributions within a thermoset composite profile. The aim of our work is to study the influence of a rubbery phase added to the epoxy matrix in production conditions. The results have shown that the rubber modified systems have a low exothermic temperature peak value, so that neither the amount of cured resin nor the final product properties are limited. First of all we will show that the phase transition (gelation and vitrification) zones within the die change as the amount of rubber varies …

Exothermic reactionPhase transitionMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringComposite numberrubberThermosetting polymerpultrusionEpoxyIndustrial and Manufacturing EngineeringSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNatural rubberPultrusionvisual_artPhase (matter)visual_art.visual_art_mediumMaterials Chemistrycuring reactionphase trasitionComposite material
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Microflow Technology in Polymer Synthesis

2012

Microflow technology, i.e., the use of microfluidic devices for continuous flow synthesis, represents a highly useful and increasingly popular method in organic chemistry. Recently, also an increasing number of polymer synthesis protocols attain benefit from this technique. In particular, the control of highly exothermic, fast polymerization reactions can be improved due to the excellent heat and mass transfer within the small dimensions of the microreactors. Continuous flow setups with different micromixer geometries and flow patterns are currently used for the preparation of a variety of macromolecular architectures by ionic and (controlled) radical polymerization techniques. This Perspec…

Exothermic reactionchemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationMicrofluidicsCationic polymerizationMicromixerNanotechnologyPolymerInorganic ChemistryPolymerizationchemistryMaterials ChemistryMicroreactorMacromolecules
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