Search results for " Catalyst"
showing 10 items of 292 documents
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.
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.
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·
Effect of catalyst composition on chain‐end‐group of polyethylene produced by salen‐type complexes of titanium, zirconium, and vanadium
2010
The chain end structures of polyethylenes produced by salen complexes of titanium, zirconium, and vanadium, activated by MAO or common alkylaluminium compounds were investigated by 1H NMR and FTIR spectroscopy. The polymerization process with the use of vanadium complexes was found to produce polymers with only vinyl end groups in practice. In the processes catalyzed by titanium and zirconium complexes activated by MAO or Et2AlCl, not only β‐hydrogen elimination and/or chain transfer to the monomer occurs but also the chain termination reaction takes place in which an organoaluminium cocatalyst is involved. That reaction proceed particularly easily in the systems: titanium complex/Et2AlCl.
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…
Effect of sample preparation on gel permeation chromatography results of determination of molecular weight of polyethylene obtained with using of zir…
2003
Molecular weights of polyethylene (PE) obtained with using of zirconocene catalyst activated with large excess of methylaluminoxane (MAO) were determined by gel permeation chromatography (GPC) method. It was found that repeatability of the measurements is strongly influenced by MAO remained in PE samples as well as time of sample keeping in the apparatus (dissolution + measurement time) at temp. 142 °C. A method of MAO removing from PE samples, before GPC measurement, based on additional washing of the sample with HF in methanol solution has been proposed. This modification leads to better both authenticity and repeatability of the results. Studies on the influence of time of sample keeping…
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 using vanadium catalyst supported on silica modified by pyridinium ionic liquid
2016
Vanadium catalyst systems (SIL1–3A(B)/V) for ethylene polymerization were obtained by immobilization of the Cp2VCl2precursor (V) in the ionic liquid -[3-(triethoxysilyl)propyl]pyridinium chloride (IL), modified by AlCl3 and AlEtCl2(A) or AlEt2Cl (B), and supported on three types of silica carrier S1–3. The properties of the ionic liquid supports were determined using Fourier transform infrared spectroscopy, Brunauer–Emmett–Teller measurements, scanning electron microscopy and elemental analysis. The best results (above 2 tons PE (mol V)−1(0.5 h)−1) were obtained using the catalyst system SIL3B/V. Addition of ethyl trichloroacetate is possible in the ionic liquid medium and it further increas…
Direct synthesis of fibrous high molecular weight polyethylene using vanadium catalysts supported on an SiO2 ionic liquid system
2015
Polyethylene of fibrous morphology was obtained using Cp2VCl2 and VCl2(salenCl2) catalysts activated by AlEt2Cl and AlEtCl2 and heterogenized on a supported ionic liquid system prepared with SiO2 and 1-(3-triethoxysilyl)propyl-3-methylimidazolium chloroaluminate. The fibre length ranges from 15 to 60 µm, depending on the reaction conditions. The polyethylene is characterized by a high molecular weight ((1.1–2.4) × 106 g mol−1) and a narrow molecular weight distribution (1.4–2.5). It is a linear polymer, properly without branching. The DSC method reveals characteristic changes in melting temperature and crystallinity degree between the first and second scan heating cycles (141 °C and 136 °C,…
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.