Search results for "Copolymer"

showing 10 items of 1003 documents

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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Polypropylene and poly(ethylene-co-1-octene) effective synthesis with diamine-bis(phenolate) complexes: Effect of complex structure on catalyst activ…

2017

A series of group 4 metal complexes bearing amine-bis(phenolate) ligands with the amino side-arm donor: (μ-O)[Me2N(CH2)2N(CH2-2-O-3,5-tBu2-C6H2)2ZrCl]2 (1a), R2N(CH2)2N(CH2-2-O-3-R1-5-R2-C6H2)2TiCl2 (R = Me, R1, R2 = tBu (2a), R = iPr, R1, R2 = tBu (2b), R = iPr, R1 = tBu, R2 = OMe (2c)), and Me2N(CH2)2N(CH2-2-O-3,5-tBu2-C6H2)(CH2-2-O-C6H4)TiCl2 (2d) are used in ethylene and propylene homopolymerization, and ethylene/1-octene copolymerization. All complexes, upon their activation with Al(iBu)3/Ph3CB(C6F5)4, exhibit reasonable catalytic activity for ethylene homo- and copolymerization giving linear polyethylene with high to ultra-high molecular weight (600·× 103–3600·× 103 g/mol). The activi…

EthylenePolymers and Plastics010405 organic chemistryComonomerOrganic Chemistrydiamino-bis(phenolate) catalystsmicrostructurepoly(ethylene-co-1-octene)Ziegler-Natta polymerization010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisLinear low-density polyethylenechemistry.chemical_compoundchemistryPolymerizationDiaminePolymer chemistryMaterials ChemistryCopolymer1-OctenepolypropyleneJournal of Polymer Science Part A-Polymer Chemistry
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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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Grafting of Hindered Phenol Groups onto Ethylene/α-Olefin Copolymer by Nitroxide Radical Coupling

2017

The covalent immobilization of hindered phenol groups, with potential antioxidant activity, onto an ethylene/α-olefin (EOC) copolymer was carried out by the nitroxide radical coupling (NRC) reaction performed in the melt with a peroxide and the 3,5-di-tert-butyl-4-hydroxybenzoyl-2,2,6,6-tetramethylpiperidine-1-oxyl radical (BHB-T). Functionalized EOC (EOC-g-(BHB-T)) was exposed to photo- and thermo-oxidation. By comparison with some model compounds bearing the (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) moiety or the hindered phenol unit, it was observed that the grafted BHB-T could effectively help the stabilization of the polymer matrix both under photo- and thermo-oxidation. In addit…

EthylenePolymers and Plastics02 engineering and technology010402 general chemistry01 natural sciencesPeroxideArticlelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrynitroxide radical couplingPolymer chemistryCopolymerMoietyantioxidant covalent immobilizationchemistry.chemical_classificationOlefin fiberhindered phenol moietyChemistry (all)General ChemistryPolymer021001 nanoscience & nanotechnologyGrafting0104 chemical scienceschemistryCovalent bondantioxidant covalent immobilization; nitroxide radical coupling; hindered phenol moiety; HAS-NOR antioxidant0210 nano-technologyHAS-NOR antioxidantPolymers
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Vanadium complex with tetradentate [O,N,N,O] ligand supported on magnesium type carrier for ethylene homopolymerization and copolymerization

2009

Immobilization of 1,2-cyclohexylenebis(5-chlorosalicylideneiminato)vanadium dichloride on the magnesium support obtained in the reaction of MgCl 2 .3.4EtOH with Et 2 AlCl gives a highly active precursor for ethylene homopolymerization and its copolymerization with 1-octene. This catalyst exhibits the highest activity in conjunction with MAO, but it is also highly active with AlMe 3 as a cocatalyst. On the other hand, when combined with chlorinated alkylaluminum compounds, Et 2 AlCl and EtAlCl 2 , it gives traces of polyethylene. Moreover, its catalytic activity is strongly affected by the reaction temperature: it increased with rising polymerization temperature from 20 °C to 60 °C, The kine…

EthylenePolymers and PlasticsChemistryMagnesiumOrganic Chemistrychemistry.chemical_elementVanadiumPolyethyleneCatalysischemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistryCopolymerTitaniumJournal of Polymer Science Part A: Polymer Chemistry
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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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“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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Dichlorovanadium(IV) diamine-bis(phenolate) complexes for ethylene (co)polymerization and 1-olefin isospecific polymerization

2018

Abstract Two vanadium complexes bearing amine-bis(phenolate) ligands with the amino side-arm donor, [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)2}Cl2] (1) and [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)(CH2-2-O-C6H4)}Cl2] (2), were synthesised and characterized by FTIR and 1H NMR spectroscopy. Upon activation with Al(iBu)3/Ph3CB(C6F5)4, these complexes became active catalysts for 1-octene polymerization giving highly stereoregular polymers (mmmm ∼ 90%) having regioirregularly arranged units. The catalytic activity of the catalysts in ethylene homo- and copolymerization, and their ability to incorporate a comonomer were highly dependent on both the activator type and the complex structure. 1/EtAlCl2 exhi…

EthylenemicrostructureDispersityZiegler-Natta polymerization010402 general chemistry01 natural sciencesCatalysisTREFchemistry.chemical_compoundDiaminediamine-bis(phenolate) ligandPolymer chemistryethyleneCopolymerPhysical and Theoretical Chemistrychemistry.chemical_classificationOlefin fiber010405 organic chemistryChemistryComonomerPolymer0104 chemical sciencescopolymerizationVanadium catalystPolymerization1-octeneJournal of Catalysis
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Hyaluronan-Based Graft Copolymers Bearing Aggregation-Induced Emission Flurogens

2017

In order to develop a technology platform based on two natural compounds from biorenewable resources, a short series of hyaluronan (HA) copolymers grafted with propargylated ferulic acid (HA-FA-Pg) were designed and synthesized to show different grafting degree values and their optical properties were characterized in comparison with reference compounds containing the same ferulate fluorophore. Interestingly, these studies revealed that the ferulate fluorophore was quite sensitive to the restriction of intramolecular motion and its introduction into the rigid HA backbone, as in HA-FA-Pg graft copolymers, led to higher photoluminescence quantum yield values than those obtained with the isola…

FluorophoreGeneral Chemical EngineeringfluorogenSQuantum yield02 engineering and technology010402 general chemistry01 natural sciencesFerulic acidhyaluronanchemistry.chemical_compoundCopolymerChemical Engineering (all)Aqueous solutionAGGREGATION INDUCED EMISSIONChemistryChemistry (all)General Chemistry021001 nanoscience & nanotechnologyGraftingCombinatorial chemistry0104 chemical sciencesSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPropargylChemistry (all); Chemical Engineering (all)0210 nano-technologyEthylene glycolAggregation-induced emissionsAqueous environmentBiomedical applicationsferulic acid
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