Search results for "POLYMERIZATION"
showing 10 items of 1689 documents
Effect of immobilization of titanocene catalyst in aralkyl imidazolium chloroaluminate media on performance of biphasic ethylene polymerization and p…
2012
1-(2-Phenylethyl)-3-methylimidazolium and 1-benzyl-3-methylimidazolium chloroaluminates, [Ph-C2mim][AlCl4] and [Bzlmim][AlCl4], were applied as media of the Cp2TiCl2 catalyst for biphasic ethylene polymerization. The studied aralkyl ionic liquids ensure greater stability of the catalyst at higher temperatures and more regular morphology of the produced polyethylene than analogous 1-n-alkyl-3-methylimidazolium chloroaluminates. The alkylaluminium compound participates in the termination reaction of the polymer chain. The catalyst is stable and enables recycling of the ionic liquid phase in the consecutive polymerization reactions. The [Ph-C2mim][AlCl4] ionic liquid and AlEt2Cl alkylaluminium…
Ethylene polymerization with FI complexes having novel phenoxy‐imine ligands: Effect of metal type and complex immobilization
2011
A series of bis(phenoxy‐imine) vanadium and zirconium complexes with different types of R3 substituents at the nitrogen atom, where R3 = phenyl, naphthyl, or anthryl, was synthesized and investigated in ethylene polymerization. Moreover, the catalytic performance was verified for three supported catalysts, which had been obtained by immobilization of bis[N‐(salicylidene)‐1‐naphthylaminato]M(IV) dichloride complexes (M = V, Zr, or Ti) on the magnesium carrier MgCl2(THF)2/Et2AlCl. Catalytic performance of both supported and homogeneous catalysts was verified in conjunction with methylaluminoxane (MAO) or with alkylaluminium compounds (EtnAlCl3−n, n = 1–3). The activity of FI vanadium and zirc…
Synteza bimetalicznego silseskwioksanowego kompleksu tytanu(IV) i jego polimerycznego odpowiednika oraz ich właściwości katalityczne w polimeryzacji …
2016
Zsyntetyzowano, a następnie scharakteryzowano dwa tytanosilseskwioksany: nowy, nieznany dotąd z literatury, tetrachloroditytanosilseskwioksan (2) i jego polimeryczny odpowiednik (3). Zbadano właściwości katalityczne otrzymanych związków w polimeryzacji etylenu i 1-oktenu. Obydwa prekatalizatory, po aktywacji za pomocą Et2AlCl lub EtAlCl2, katalizują polimeryzację etylenu do polietylenu (PE) o małej masie molowej, która zmniejsza się zarówno ze wzrostem temperatury reakcji, jak i stosunku molowego Al:Ti. Kompleks (2) w połączeniu z metyloaluminoksanem lub związkami boru jest także aktywny w polimeryzacji 1-oktenu.
Ethylenebis(5‐chlorosalicylideneiminato)vanadium dichloride immobilized on MgCl2‐based supports as a highly effective precursor for ethylene polymeri…
2009
Ethylenebis(5‐chlorosalicylideneiminato)vanadium dichloride supported on MgCl2(THF)2 or on the same carrier modified by EtnAlCl3−n, where n = 1–3, was used in ethylene polymerization in the presence of MAO or a common alkylaluminium compounds as a cocatalyst. The support type alter vanadium loading and also change the characteristic of the catalytic active sites. Et2AlCl is the best activator for a catalyst which has been immobilized on a nonmodified support, whereas the systems which contain a carrier which has been modified by an organoaluminium compound reveal the highest activity in conjunction with MAO. That difference, together with different temperature effects on polymerization effi…
Dichlorovanadium (IV) complexes with salen‐type ligands for ethylene polymerization
2008
Vanadium complexes with tetradentate salen‐type ligands were first time explored in ethylene polymerizations. The effects of the vanadium complex structure, the alkyl aluminum cocatalysts type (EtAlCl2, Et2AlCl, Et3Al, and MAO), and the polymerization conditions (Al/V molar ratio, temperature) on polyethylene yield were explored. It was found that EtAlCl2 in conjunction with investigated vanadium complexes produced the most efficient catalytic systems. It was shown, moreover, that the structural changes of the tetradentate salen ligand (type of bridge which bond donor nitrogen atoms and type of substituent on aryl rings) affected activity of the catalytic system. The complexes containing li…
Nature of activating effect of two‐step polymerization of propylene
1999
The prepolymerization effect on propylene polymerization in the presence of a TiCl3‐based catalyst, modified by di‐n‐buthyl ether, was studied. The influence of prepolymerization on the electron spin resonance spectra and morphology of the catalyst, as well as the properties and the morphology of both prepolymer and regular polymerization products, was investigated. The polymer morphology was evaluated through scanning electron microscopy, polymer bulk density, and particle size distribution. Some evidence of the enhancement effect of prepolymerization on the catalyst activity and stereospecificity was obtained. No influence from prepolymerization was observed on molecular weight and its di…
Synthesis and catalytic properties for olefin polymerization of new vanadium complexes containing silsesquioxane ligands with different denticity
2017
A series of new vanadium-silsesquioxanes (2a − 2d) was prepared by reacting VCl4 with not fully condensed silsesquioxanes (having from one to four silanol groups) and evaluated as pre-catalysts in olefin polymerization. The activation of 2a − 2d with EtAlCl2 generated highly active catalysts for ethylene polymerization, yielding high molar mass polymers with narrow dispersity. Ultra-high molar mass polyethylenes, Mw up to 4 × 106 g mol−1, were obtained with methylaluminoxane and Al(iBu)3/[Ph3C][B(C6F5)4] as activators. Upon treatment with methylaluminoxane and boron compounds, all vanadium pre-catalysts were active in 1-octene polymerization as well, and produced isotactic-rich poly(1-octen…
Recycling ground tire rubber (GTR) scraps as high-impact filler of in-situ produced polyketone matrix
2014
Block copolymers from ionic liquids for the preparation of thin carbonaceous shells
2017
This paper describes the controlled radical polymerization of an ionic-liquid monomer by RAFT polymerization. This allows the control over the molecular weight of ionic liquid blocks in the range of 8000 and 22000 and of the block-copolymer synthesis. In this work we focus on block copolymers with an anchor block. They can be used to control the formation of TiO2 nanoparticles, which are functionalized thereafter with a block of ionic-liquid polymer. Pyrolysis of these polymer functionalized inorganic nanoparticles leads to TiO2 nanoparticles coated with a thin carbonaceous shell. Such materials may, e.g., be interesting as battery materials.
Effect of hydrogen on the ethylene polymerization process over Ziegler–Natta catalysts supported on MgCl2(THF)2. II. Kinetic studies
2001
This article reports on a study of the effects of hydrogen on the activity of vanadium and titanium catalysts supported on MgCl2(THF)2 in ethylene polymerization. It was found that hydrogen did not change the stable nature of the active sites and the polydispersity index of the polyethylene obtained. The propagation rate, expressed as kp, was found to be independent of the presence and concentration of hydrogen, indicating that this reacting agent does not modify the reactivity of the active sites. However, the presence of hydrogen in the polymerization medium is responsible for partial deactivation of the active sites just before polymerization is initiated.