Search results for "POLYMERIZATION"

showing 10 items of 1689 documents

Polimeryzacja koordynacyjna alkenylosilseskwioksanów i ich kopolimeryzacja z olefinami lub styrenem

2015

Artykuł stanowi kontynuację przeglądu literatury dotyczącej koordynacyjnej polimeryzacji silseskwioksanów (POSS), zawierających zdolne do polimeryzacji wiązanie podwójne, oraz ich kopolimeryzacji głównie zolefinami, a także ze styrenem. Zastosowanie katalizatorów metalocenowych aktywowanych metyloaluminoksanem (MAO) zapewnia efektywną (ko)polimeryzację silseskwioksanów zarówno z olefinami, jak i styrenem. Wprowadzenie do materiału polimerowego komonomeru POSS korzystnie wpływa na właściwości otrzymanych produktów, które cechują się większą odpornością termiczną oraz wytrzymałością mechaniczną niż ich odpowiedniki niezawierające POSS.

poliedryczne oligomeryczne silseskwioksany (POSS)coordination (co)polymerization(ko)polimeryzacja koordynacyjnametallocene catalyststhermal propertieswłaściwości termicznemechanical propertieskatalizatory metalocenowewłaściwości mechanicznepolyhedral oligomeric silsesquioxanes (POSS)Polimery
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Silseskwioksany i ich zastosowanie w syntezie materiałów polimerowych

2015

Artykuł stanowi przegląd literatury dotyczącej syntezy oraz charakterystyki materiałów polimerowych zawierających silseskwioksany (POSS). Przedstawiono metody otrzymywania hybrydowych materiałów polimerowych z udziałem funkcjonalizowanych POSS na drodze click chemistry, polikondensacji, poliaddycji, metatezy z otwarciem pierścienia ipolimeryzacji rodnikowej zarówno konwencjonalnej, jak i kontrolowanej (ATRP).

poliedryczne oligomeryczne silseskwioksany (POSS)ring opening metathesis polymerizationpolimeryzacja wolnorodnikowamateriały hybrydoweATRPpoliaddycjapolikondensacjametateza z otwarciem pierścieniaclick chemistryhybrid materialspolycondensationpolyadditionfree-radical polymerizationpolyhedral oligomeric silsesquioxane (POSS)Polimery
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Hetero-difunctional dimers as building blocks for the synthesis of poly(amidoamine)s with hetero-difunctional chain terminals and their derivatives

2012

This article reports on a simple and straightforward preparation method of poly(amidoamine)s (PAAs) with hetero-difunctional chain ends as well as of several up to now hardly obtainable PAA derivatives of biotechnological interest, such as for instance PAAs of controlled molecular weight and narrow polydispersity mono-functionalized at one end with an acrylamide group, PAAs with star-like molecular architecture, graft-PAA-protein conjugates, “tadpole-like” PAA conjugates with hydrophobic moieties able to self assemble into nanoparticles in aqueous media. The key step was to design suitable building blocks consisting of hetero-difunctional dimers (HDDs). In particular, the HDDs considered we…

poly(amidoamine)Materials Chemistry2506 Metals and AlloyPolymers and PlasticPolymers and PlasticsChemistrynanoparticleOrganic ChemistryAmidoamineDispersityamphiphileNanoparticlePoly(amidoamine)star polymerchemistry.chemical_compoundChain (algebraic topology)PolymerizationpolyamineAmphiphilePolymer chemistryMaterials Chemistryprotein graftingConjugateJournal of Polymer Science Part A: Polymer Chemistry
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Acid-Labile Surfactants Based on Poly(ethylene glycol), Carbon Dioxide and Propylene Oxide: Miniemulsion Polymerization and Degradation Studies

2017

Partially degradable, nonionic AB and ABA type di- and triblock copolymers based on poly(propylene carbonate) and poly(ethylene glycol) blocks were synthesized via immortal copolymerization of carbon dioxide and propylene oxide, using mPEG or PEG as a macroinitiator, and (R,R)-(salcy)-CoOBzF5 as a catalyst in a solvent-free one-pot procedure. The amphiphilic surfactants were prepared with molecular weights (Mn) between 2800 and 10,000 g·mol−1 with narrow molecular weight distributions (1.03–1.09). The copolymers were characterized using 1H-, 13C- and DOSY-NMR spectroscopy and size exclusion chromatography (SEC). Surface-active properties were determined by surface tension measurements (crit…

polycarbonate; CO2; surfactant; miniemulsion polymerization; degradation; nanoparticleMaterials sciencePolymers and Plasticssurfactant02 engineering and technology010402 general chemistry01 natural sciencesArticleStyrenelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPolymer chemistryCopolymerPropylene oxidedegradationnanoparticleGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMiniemulsionpolycarbonateChemical engineeringPolymerizationchemistryminiemulsion polymerizationCritical micelle concentrationPropylene carbonateCO20210 nano-technologyEthylene glycolPolymers
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Metallocenes and post-metallocenes immobilized on ionic liquid-modified silica as catalysts for polymerization of ethylene

2014

Abstract The supported ionic liquid (SIL) strategy was used for the first time to metallocene and post-metallocene heterogeneous catalysts for olefin polymerization. The metal complexes: Cp2TiCl2, Cp2ZrCl2, FI–Ti, and Sal–Ti were immobilized in the 1-(3-triethoxysilyl)propyl-3-methylimidazolium alkylchloroaluminate ionic liquid, anchored on the surface of the mesoporous amorphous silica. The SIL systems were characterized by FTIR, 29Si NMR, N2 adsorption, EA, AAS, TG, and SEM techniques. The developed supported catalytic systems were found to be active in the ethylene polymerization and produce the polyethylene of various properties.

polyethyleneChemistryProcess Chemistry and TechnologyPost-metallocene catalystPolyethyleneCatalysischemistry.chemical_compoundAdsorptionPolymerizationsilicaIonic liquidPolymer chemistryorganometallic catalystCoordination polymerizationMesoporous materialMetalloceneionic liquidApplied Catalysis A : General : an International Journal Devoted to Catalytic Science and its Applications
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Naturally Occurring Oxazole Structural Units as Ligands of Vanadium Catalysts for Ethylene-Norbornene (Co)polymerization

2021

1,3-Oxazole and 4,5-dihydro-1,3-oxazole are common structural motifs in naturally occurring peptides. A series of vanadium complexes were synthesized using VCl3(THF)3 and methyl substituted (4,5-dihydro-1,3-oxazol-2-yl)-1,3-oxazoles as ligands and analyzed using NMR and MS methods. The complexes were found to be active catalysts both in ethylene polymerization and ethylene-norbornene copolymerization. The position of methyl substituent in the ligand has considerable impact on the performance of (co)polymerization reaction, as well as on the microstructure, and thus physical properties of the obtained copolymers.

polyethyleneEthyleneSubstituentVanadiumchemistry.chemical_elementTP1-1185010402 general chemistry01 natural sciencesCatalysisCatalysischemistry.chemical_compoundPolymer chemistryCopolymervanadium catalystPhysical and Theoretical ChemistryQD1-999polyethylene; norbornene copolymers; oxazole ligand; vanadium catalyNorborneneOxazole010405 organic chemistryChemical technology0104 chemical sciencesChemistrychemistryPolymerizationnorbornene copolymersoxazole ligandCatalysts
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Titanium and Vanadium Catalysts with 2-Hydroxyphenyloxazoline and Oxazine Ligands for Ethylene-Norbornene (co)Polymerization

2019

A series of titanium and vanadium complexes with oxazoline 2-(4,5-dihydro-1,3-oxazol-2-yl)phenol (L1), 2-(4-methyl-4,5-dihydro-1,3-oxazol-2-yl)phenol (L2), and oxazine 2-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenol (L3) ligands were synthesized, and their structures were determined by NMR and MS methods as (L)2MtCl2. The vanadium complexes were found to be highly active in ethylene (7300 kgPE/(molV&middot

polyethyleneEthyleneoxazine ligandVanadiumchemistry.chemical_elementPolyethyleneCatalysisCatalysischemistry.chemical_compoundchemistryPolymerizationnorbornene copolymersPolymer chemistryCopolymervanadium catalystMolar mass distributionPhysical and Theoretical Chemistryoxazole ligandNorborneneCatalysts
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A supported titanium postmetallocene catalyst: Effect of selected conditions on ethylene polymerization

2011

Ethylene polymerization with a titanium complex [N,N-ethylenebis(3-methoxysalicylideneiminato)titanium dichloride] immobilized on the magnesium support with the formula MgCl2(THF)0.32(Et2AlCl)0.36 was studied. In particular, the effects of polymerization temperature, monomer pressure, and polymerization time on the activity of the catalyst and on the polyethylene properties (molecular weight and its distribution, melting point, crystallinity, and bulk density) were evaluated. The findings of investigations prove that the studied supported titanium catalyst is highly active in ethylene polymerization, and its activity increases with increasing temperature and monomer pressure. Moreover, stab…

polyethyleneMaterials sciencePolymers and PlasticsBulk polymerizationsupportsmelting pointtechnology industry and agriculturechemistry.chemical_elementSolution polymerizationGeneral Chemistrymolecular weight distributionPolyethylenecatalystsSurfaces Coatings and Filmschemistry.chemical_compoundChain-growth polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryPrecipitation polymerizationCoordination polymerizationTitaniumJournal of Applied Polymer Science
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Transition metal complexes of tetradentate and bidentate Schiff bases as catalysts for ethylene polymerization: Effect of transition metal and cocata…

2009

This article compares catalytic performance of ethylene polymerization in similar polymerization conditions of transition metal complexes having two ligands [O,N] (phenoxy-imine) and having one tetradentate ligand [O,N,N,O] (salphen or salen). It is shown that the activity of both complex types as well as the product properties depend in the same way on the type of central metal in the complex and on the cocatalyst used. Although the type of ligand has some effect on the catalyst activity, yet it does not control the properties of the obtained products. The vanadium and zirconium complexes, irrespective of the cocatalyst used, yield linear polyethylene with high molecular weight (a few hund…

polyethyleneZiegler‐Natta polymerizationDenticitySchiff basePolymers and PlasticsChemistryLigandOrganic ChemistryVanadiumchemistry.chemical_elementPolyethyleneCatalysischemistry.chemical_compoundpostmetallocene catalystTransition metalPolymerizationPolymer chemistryMaterials ChemistrySchiff basesoligomersJournal of Polymer Science. Part A : Polymer Chemistry
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Vanadium complex with tetradentate [O,N,N,O] ligand supported on magnesium type carrier for ethylene homopolymerization and copolymerization

2010

Immobilization of 1,2‐cyclohexylenebis(5‐chlorosalicylideneiminato)vanadium dichloride on the magnesium support obtained in the reaction of MgCl2·3.4EtOH with Et2AlCl 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 AlMe3 as a cocatalyst. On the other hand, when combined with chlorinated alkylaluminum compounds, Et2AlCl and EtAlCl2, 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 kinetic curve…

polyethyleneZiegler‐Natta polymerizationcopolymerizationsupportsvanadium complexJournal of Polymer Science. Part A : Polymer Chemistry
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