Patent Application
20110178258
The present invention relates to the covalent anchorage of non-coordinating anions on mineral supports to prepare supported ionic liquids and to their use as activating agents for the polymerisation of ethylene and alpha-olefins. The invention also discloses the concomitant covalent anchorage of zwitterionic systems containing both the non-coordinating anion and the counter cation parts of the ionic liquids and of the activating agents.
It is known that perfluorinated borates can be covalently anchored on different supports such as for example polystyrene and silica. This was reported in U.S. Pat. No. 5,427,991 or in U.S. Pat. No. 5,869,723 or in EP-A-1359166 or in WO03/035708. The counter cations of the grafted perfluorinated borate were anilinium-type or trityl cations when these solid systems were used to activate catalyst components in the polymerisation of ethylene and alpha-olefins. In parallel, various works were reported in literature concerning the direct chemisorption of tris (pentafluorophenyl)borane on silica surface such as for example J. Tian, S. Wang, Y. Feng, J. Li, S. Collins, “Borane-functionalized oxide supports: development of active supported metallocene catalysts at low aluminoxane loading” in J. Mol. Catal. A: Chemical, 1999, 144, 137-150, or in M. Bochmann, G. J. Pindado, S. J. Lancaster, “The versatile chemistry of metallocene polymerisation catalysts: new developments in half-sandwich complexes and catalyst heterogenisation.” in J. Mol. Catal. A: Chemical, 1999, 146, 179-190, or in S. Charoenchaidet, S. Chavadej, E. Gulari, “Borane-functionalized silica supports in situ activated heterogeneous zirconocene catalysts for MAO-free ethylene polymerisation” in J. Mol. Catal. A: Chemical, 2002, 167-177, 185, or in K. Musikabhumma, T. P. Spaniol, J. Okuda, “Ethylene polymerization with “constrained-geometry” titanium catalysts over borate-modified silica supports” in Macromol. Chem. Phys., 2002, 203, 115-121. This strategy additionally requires the presence of trityl or substituted ammonium (preferably dimethylanilinium) as countercations.
These catalytic systems using supported activators are less active than equivalent homogeneous systems and the polymer properties are thereby degraded.
A new generation of solid activating supports has been developed and is described for example in Marks (J. Am. Chem. Soc., 1998, 120, 13533): it concerns sulfated zircone particles or in McDaniel (WO-9960033, WO-0123433, WO-0123434, WO-0144309, WO-0149747 et U.S. Pat. No. 6,548,441) or in Saudemont (FR-A-2765225). All these activators are solids wherein surface acid sites are responsible for the activation.
These acid sites are metals combined with halides such as fluor or chlorine; metals can be selected from aluminium, titanium, zirconium or nickel.
The equivalent species in homogeneous catalysis are very poor activating species.
Compounds such as dimethylaluminium fluoride (DMAF) are used as activators in combination with triethylaluminium for the stereospecific polymerisation of propylene with compounds of the metallocene family with low productivity as described by Zambelli (Macromolecules 1989, 22, 2186). They do not activate metallocene complexes.
On the other hand, ionic liquids are also actively investigated as alternative solvent media in many industrial applications such as synthesis, catalysis, separation, electrochemistry or nanoparticles stabilisation (“Ionic Liquids—Industrial Applications to Green Chemistry” ACS Symposium Series, Eds R D. Rogers and K. S. Seddon, American Chemical Society, Washington, D.C., 2001; “Innovative Applications of Ionic Liquids as “Green Engineering Liquids” H. Zhao, Chem. Eng. Comm., 2006, 193, 1660-1677). Synthesis is described for example in K. R. Seedon, Kinetic Catal., 1996, 37, 693; or in J. Howarth, Tetrahedron Lett., 2000, 41, 6627; or in F. Zulfiquar, G. Tanaka, Green Chemistry, 2000, 2, 6627. Catalysis is described for example in “Catalytic reactions in ionic liquids” R. Sheldon, Chem. Commun., 2001, 2399-2407; or in J. J. Peng, Y. Q. Deng, New J. Chem., or in “Ionic liquids in Catalysis” T. Welton, Coord. Chem. Rev., 2004, 248, 2459-2477. Separation is described for example in H. Qiu, S. Jiang, X. Liu, J. Chromatography A, 2006, 1103, 265-270; or in H. Qiu, S. Jiang, X. Liu, L. Zhao, J. Chromatography A, 2006, 1106, 46-50. Electrochemistry is described for example in J. Dupont, R. F. de Souza, P. A. Z. Suarez, Chem. Rev., 2002, 102, 3667-369. Nanoparticle stabilisation is described for example in “The use of imidazolium ionic liquids for the formation and stabilization of Ir0 and Rh0 nanoparticles: efficient catalysts for the hydrogenation of arenes” G. S. Fonseca, A. P. Umpierre, P. F. P. Fichtner, S. Teixeira, Chem. Eur. J. 2003, 9, 3263-3269.
Perfluoroalkyltrifluoroborates were also used as counter anions for ionic liquids, particularly to stabilise cyclic quaternary ammonium as disclosed for example in “Cyclic quaternary ammonium ionic liquids with perfluoroalkyltrifluoroborates: synthesis, characterization, and properties” Z.-B. Zhou, H. Matsumoto, K. Tatsumi, Chem. Eur. J., 2006, 12, 2196-2212. Until now, ionic liquids have been covalently anchored on silica surface by means of their cationic part using silica silylating reagent such as 1-methyl-3-(3-triethoxysilyl)-propylimidazolium cation as disclosed for example in WO2002098560, or in WO2001032308, or in M. H. Valkenberg, C. de Castro, W. F. Höelderich, Green Chemistry, 2002, 4, 88-93, or in C. P. Mehnert, R. A. Cook, N. C. Dispenziere, M. Afework, J. Am. Chem. Soc., 2002, 124, 12932.
The ionic liquids can also be anchored by their anionic part: this is achieved by co-deposition of chloroaluminate species anion on silica with the 1-butyl-3-methyl-imidazolium (bmim) as counter cation.
N-[(trifluoromethyl)sulfony] trifluoromethanesulfonimide or bis-((perfluoromethyl)sulfonyl)imide (TFMSI) is currently used as counter anion in ionic liquids in order to impart to the resulting ionic liquid, particular physico-chemical properties. This is described for example in “Synthesis of 2,2-biimidazolium-based ionic liquids: use as a new reaction medium and ligand for palladium-catalyzed Suzuki cross-coupling reactions” J-C. Xiao, J. M. Shreeve, in J. Org. Chem., 2005, 70, 3072-3078, or in “Lithium ion conduction in a organoborate zwitterion-LiTFSI mixture” A. Narita, W. Shibayama, K. Sakamoto, T. Mizumo, N. Matsumi, H. Ohno, in Chem. Commun, 2006, 1926-1928.
One of the objectives of this invention is the use of heterogenised perfluorinated aryl borates covalently grafted on silica, as counter anions, to stabilise cations such as 1,3-dialkyl-imidazolium or 1-alkyl-pyridinium or related systems, in order prepare supported ionic liquids.
Another aim of the present invention is the co-anchorage of two parts of ionic liquids onto a support: the anion and the cation.
It is a further goal of the present invention to prepare supported ionic liquids from N[(perfluoroalkyl)sulfonyl] perfluoroalkane sulfonimide (PFSI) anions covalently anchored on mineral support and to use them as activating supports for the polymerisation of ethylene and alpha-olefins.
It is an aim of the present invention to prepare new species of activating support.
It is another aim of the present invention to prepare very active single site supported catalyst systems that do not require the use of methylaluminoxane.
It is also an aim of the present invention to prepare polymers that have regular grain size.
Any one of these aims is at least partially fulfilled by the present invention.
The present invention relates to the covalent anchorage of non-coordinative perfluorinated anions on mineral oxide support.
Accordingly, the present invention discloses the preparation of covalently anchored N[(perfluoroalkyl)sulfonyl]perfluoroalkanesulfonamide system as precursors for the preparation of supported ionic liquids that can be used as activating supports suitable for the polymerisation of ethylene and alpha-olefins.
Perfluoroalkanesulfonic acid-containing solids, generally called “Nafion” type-functionalised silica, have been previously reported by Harmer et al. (“Unique silane modified perfluorosulfonic acids as versatile reagents for new solid acid catalysts” M. A. Harmer, Q. Sun, M. J. Michalczyk, Z. Yang, in Chem. Commun., 1997, 1803-1804; or in “Novel mesoporous silica-perfluorosulfonic acid hybrids as strong heterogeneous Brönsted catalysts” D. J. Macquarrie, S. J. Taverner, M. A. Harmer, in Chem. Commun., 2005, 263-265) and by Corma et al. (“Single-step preparation and catalytic activity of mesoporous MCM-41 and SBA-15 silicas functionalized with perfluorosulfonic acid groups analogous to Nafion” M. Alvaro, A. Corma, D. Das, V. Fornes, H. Garcia, in Chem. Commun., 2004, 956-957; or in “Nafion” functionalized mesoporous MCM-41 silica shows high activity and selectivity for carboxylic acid esterification and Friedel-Crafts acylation reactions, M. Alvaro, A. Corma, D. Das, V. Fornes, H. Garcia, J. Catal., 2005, 231, 48-55; or in WO 2005051540). They were used in supported acid catalysis such as electrophilic aromatic substitution reactions and fatty acid esterification.
Corma's supported perfluorosulfonic acid is the reaction product of silica surface on trifluoromethyl-1 trifluoro 1,2,2′-ethanesultone, said latter product being the reaction product of perfluoropropene and sulphur trioxide. Alternatively supported sulfonic acid can be obtained starting from perfluorinated alkan-1ene.
There are two types of supported perfluorinated sulfonic acids respectively represented in the schemes below as starting material 1 and starting material 2.
The present invention discloses a method for preparing supported ionic liquids that comprises the steps of:
a) reacting starting supported sulfonic acid 1′ or 2 either with non-nucleophilic trimethylsilane in scheme (a) or with perfluoroalkan-2-ethyltrialkoxysilane in scheme b) in order to make the sulfonic group environment hydrophobic
wherein Rf is perfluoroalkyl group CF3(CF2)n— or (CF3)2CF(CF2)n— and wherein n is 0 or integer from 1 to 8;
b) reacting compounds 1, 1a, 1b, 2a and 2b with thionylchloride to produce respectively supported perfluorosulfonic chloride products 1c, 1d, 1e, 2d and 2e
c) reacting perfluorosulfonyl chloride group-containing solids 1c, 1d, 1e, 2d, and 2e with ammonia to prepare perfluorosulfonamides compounds 1f, 1g, 1h, 2g and 2h
d) reacting perfluorosulfonamides compounds 1f, 1g, 1h, 2g and 2h with perfluoroalkanesulfonyl chloride Rf′SO2Cl in the presence of an organic base to prepare respectively the covalently anchored N[(perfluoroalkyl)sulfonyl] perfluoroalkane sulfonamide 1i, 1j, 1k, 2j and 2k
wherein Rf′ is perfluoroalkyl group CF3(CF2)n— or (CF3)2CF(CF2)n—, wherein n is 0 or an integer from 1 to 8 and wherein Rf′ is the same as or different from Rf.
e) reacting anchored N[(perfluoroalkyl)sulfonyl] perfluoroalkane sulfonamide 1i, 1j, 1k, 2j and 2k with a metal hydroxide MOH or a metal organic derivative such as alkylate, arylate, aryl hydride or an organic base such as M-isopropyl amide or M-hexamethyldisilylazide, wherein M is a metal Group 1 of the periodic table, in order to obtain the corresponding covalently anchored N[(perfluoroalkyl)sulfonyl]− perfluoroalkane sulfonimide salts 1i′, 1j′, 1k′, 2j′ and 2k′
f) reacting the N[(perfluoroalkyl)sulfonyl]−perfluoroalkane sulfonimide salts-anchored supports of step e) with an organo-cation Cat, in order to obtain respectively compounds 1l, 1m, in, 2m and 2n
wherein Cat is trityl Ph3CX or ammonium halide R1R2R3R4N+X−, wherein X is halogen, Ph is phenyl group, and R1, R2, R3 and R4 are each independently selected from hydrocarbons having from 1 to 6 carbon atoms.
Preferably at least one of R1, R2, R3 and R4 is aromatic group, more preferably phenyl group.
Preferably, M is selected from Li, Na, K. More preferably it is Li. The preferred metal organic derivative is lithium hexamethyldisilylazide: it offers the advantage of passivating the residual silanols by trimethylsilylation.
The preferred organic base of step d) is triethylamine.
Preferably, Rf and Rf′ are the same. More preferably they both are CF3.
All supported ionic liquids according to the present invention can be used as activating supports, but not all activating supports are ionic liquids.
In a preferred embodiment according to the present invention N-alkyl-N′-3-(propyltrialkoxysilyl) imidazolium is used as counter cation for co-grafting the cationic part of the ionic liquid system and PFSI is used as anionic part.
In another embodiment according to the present invention, N[(perfluoroalkyl)sulfonyl] perfluoroalkane sulfonimide compounds 1i, 1j, 1k, 2j and 2k are synthesised in one step by reacting the perfluorosulfonyl chloride group-containing solids 1c, 1d, 1e, 2d and 2e of step b) with perflorosulfonamide Rf′SO2NH2 in presence of a solution of organic base.
In yet another embodiment according to the present invention, related to the supported perfluorosulfonic compounds of starting material 1, the reaction of step f), between compound 1i′ and an organo-cation, is replaced by addition to compound 1i′ of 1,3-diakyl-imidazolium bearing trialkoxysilyl groups (imid), that reacts with the residual hydroxyl groups of the mineral oxide surface resulting in anchorage of both the anionic and cationic parts to the support
wherein linker group L is alkane or aryl group, R′ is alkyl or aryl group, functionalised or not, and Rf and R′ f are the same or different and are perfluoroalkyl groups CF3(CF2)n— or (CF3)2CF(CF2)n− wherein n is zero or an integer from 1 to 8.
The present invention also discloses the double anchorage of zwitterionic system performed by covalently anchoring both the anionic and the cationic parts of ionic liquids on a support.
A first embodiment discloses the preparation of supported ionic liquids by covalently anchoring perfluorinated arylborate anion and 1,3-diakyl-imidazolium cation by means of the trialkoxysilyl group present in each ionic part.
wherein ArF is perfluorinated aromatic nucleus, L is an alkane or aryl linker group, R is alkyl group and R′ in functionalised or non-functionalised alkyl or aryl group.
A second embodiment discloses the co-anchorage on a mineral oxide support of N[(perfluoroalkyl)sulfonyl]−perfluoroalkane sulfonimide entities with imidazolium derivatives by means of the silylation of mineral oxide by zwitterionic species (PFSI−; imid+), wherein each component bears trialkoxysilane:
wherein R is alkyl group having from 1 to 6 carbon atoms and R′ is selected from alkyl, aryl, alkylaryl or fluorinated chains optionally bearing functional groups such as sulfonic or phosphonic derivatives to yield
The support is preferably a silica support.
The present invention also discloses the activating supports and the supported ionic liquids obtainable by the method of the present invention.
These new supported ionic liquids and activating supports are suitable for preparing catalyst systems based on single site catalyst components. Metallocene or late transition metal complex catalyst components prepared by any method known in the art can be deposited on the supported ionic liquids or activating supports of the present invention in order to provide active catalyst systems without addition of conventional activating agents such as aluminoxanes or boron-based compounds. The metallocene components that are preferably used in the present invention are fully alkylated and are based on bridged bisindenyl, bistetrahydroindenyl and cyclopentadienyl-fluorenyl. The most preferred catalyst components are selected from ethylene bis tetrahydroindenyl zirconium dimethyl, ethylene bis(2-Me,4-Ph-indenyl) zirconium dimethyl and ethylene (2-Me,4-tBut-cyclopentadienyl)(3,6-tBut-fluorenyl) zirconium dimethyl. Late transition metal complexes of the present invention preferably include α-diimine Ni complexes as disclosed by Brookhart in WO96/23010 or bis(imino)pyridyl Iron(II) or Cobalt(II) complexes as disclosed by Bristovsek et al. (G. J. P. Bristovsek, V. C. Gibson, B. S. Kimberley, P. J. Maddox, S. J. Mc Tavish, G. A. Solan, A. J. P. White, D. J. J. Williams, in Chem. Commun., 849-50, 1998) or in Small et al. (B. L. Small, M. Brookhart, A. M. A. Bennett, in J. Am. Chem. Soc., 120, 4049, 1998).
The metallocene component is preferably fully dialkylated. If it is dihalogenated, it is preferably used with an alkylating agent such as for example aluminium alkyl.
The present invention thus discloses a method for preparing an active catalyst system by the steps of:
The scavenger is preferably an alkyl aluminium. More preferably, it is trimethyl aluminium (TMA), triethyl aluminium (TEAL) or triisobutyl aluminium (TIBAL).
The active catalyst systems of the present invention are used for the oligomerisation or the homo- or co-polymerisation of ethylene and alpha-olefins. They have the advantage of being very efficient without the need to add costly and dangerous material such as methylaluminoxane.
The present invention thus discloses a method for oligomerising or homo- or co-polymerising that comprises the steps of:
The monomer is preferably ethylene or propylene. The comonomer is preferably ethylene, propylene or 1-hexene.
The starting silica support used in all examples was G5H from Grace Davison with a surface area of 513 m2·g−1 and a porous volume of 1.8 mL·g−1.
In a first step, 0.7 g (2.26 mmol) of 1-methyl-3-(3-triethoxysilyl)-propylimidazolium chloride prepared according to Kumar et al [P. Kumar, W. Vermeiren, J-P. Dath, W. F. Höelderich, Appl. Catal, 2006, 304, 131-141] were added to a solution of Li (4-triethoxysilyl-2,3,5,6-tetrafluoro-phenyl)-tris(pentafluorophenyl)borate (1.88 g; 2.26 mmol) in toluene (10 mL). The solution containing the zwitterionic bis-silylated was then filtered to remove the lithium chloride.
In parallel, 2.16 g of silica gel (Grace G5H) were treated under vacuum at a temperature of 150° C. during 12 h. After cooling under argon, the activated silica was suspended in toluene (10 mL), then 2.25 mmol of the solution containing the zwitterionic bis-silylated were poured into the stirred silica suspension under argon. The reaction mixture was stirred at room temperature during 3 h, then heated at 80° C. during 16 h. After cooling, the solid was filtered, under argon, then washed twice with 20 mL of anhydrous toluene, then twice with 20 mL of pentane. The material was treated in soxhlet extractor with 1:1 of dichloromethane: diethylether for 16 h, then evacuated under vacuum at room temperature during 4 h.
A solution of 0.8 g (3.5 mmol) of 1,2,2-trifluoro-2-hydroxy1-(trifluoromethyl)-ethane sulfonic acid beta-sultone (from ABCR chemicals) in dry toluene (20 mL) was added at room temperature to a suspension of 4 g of cooled activated silica gel ((G5H) (treated under vacuum at a temperature 150° C. during 8 h) in toluene (25 mL) under argon. After stirring at room temperature during 30 min, the reaction mixture was heated at a temperature of 80° C. during 12 h then at a temperature of 100° C. during 3 h more. After cooling, the solid was filtered under argon and washed under argon with dry toluene (30 mL, 2 times), then with pentane (20 mL) then evacuated under vacuum 4 h. Thermogravimetry analysis indicated a perfluorosulfonic loading of 0.2 mmol·g−1
Two other runs were carried out. In each run, 2.8 g of sultone (12 mmol) were contacted with 6 g of activated silica using the same procedure. Thermogravimetry analysis indicated a perfluorosulfonic loading of 0.54 mmol·g−.
3.2 g of perfluorosulfonic acid-grafted silica of samples I and II were evacuated at a temperature of 100° C. during 12 h then each sample was treated with a solution of N,O-bis-trimethylsilyl-trifluoroacetamide (2 mL) in toluene (32 mL) and stirred. Each reaction mixture was heated at a temperature of 80° C. during 12 h. The passivated perfluorosulfonic acid-grafted silicas were filtered under argon, then washed with toluene (2 times 20 mL), pentane (2 times, 20 mL) dichloromethane (2 times 20 mL), then ethyl-ether (20 mL). The two passivated solids were then evacuated under vacuum.
3.2 g of each of the passivated sulfonic acid-grafted silica samples prepared hereabove were activated at a temperature of 100° C. under vacuum during 12 h. After cooling, 40 mL of dry toluene were added under argon, followed by addition of freshly distilled SOCl2 (4 mL), corresponding to a large excess (4 equ.) of grafted sulfonic function. After stirring at room temperature during 30 min, the reaction mixtures were heated at a temperature of 110° C. during 2 h. After cooling, the excess SOCl2 was evacuated under vacuum.
First Method: Preparation of passivated 1,2,2-trifluoro-1-trifluoromethyl-ethane sulfonamide-containing silica gel
3 g of the passivated 1,2,2-trifluoro-1-trifluoromethyl-ethane sulfonyl chloride-containing silica gel obtained hereabove were poured in an autoclave (50 mL) under a stream of argon. After cooling the autoclave at a temperature of −15° C., ammonia was admitted (5.5 bars) until the ammonia condensed weight was 6 g. The autoclave was gently returned to room temperature, the reaction mixture was maintained under stirring for 3 h 30 at room temperature. Ammonia was then evacuated at normal pressure. The solid was washed with toluene (3 times, 30 mL), ethanol (30 mL), ethanol-water mixture (2 times, 30 mL), ethanol (20 mL), filtered, then washed again with ethanol (20 mL), pentane (2 times, 10 mL), then evacuated under vacuum.
To a suspension of passivated 1,2,2-trifluoro-1-trifluoromethyl-ethane sulfonamide-containing silica gel (1.5 g), previously activated at a temperature of 120° C. during 6 h, then cooled under argon, in toluene (20 mL), was added a solution of trifluoromethanesulfonyl chloride (0.68 g; 4 mmol) and triethylamine (0.4 g; 4 mmol) in toluene (15 mL).
The reaction mixture was stirred at a temperature of 80° C. during 12 h, then after cooling the solid was filtered, washed with toluene, methanol: water mixture (60:40), ethanol, ether, then with a refluxing dichloromethane: ethyl ether mixture (50:50) using a soxhlet apparatus. The solid was washed twice with pentane (30 mL) and dried under vacuum.
Second Method: Preparation of N-[(trifluoromethyl)sulfonyl]1,2,2-trifluoro-1-trifluoromethyl-ethane) sulfonamide-containing silica gel.
1,2,2-trifluoro-1-trifluoromethyl-ethane sulfonyl chloride-containing silica gel (1.6 g) was freshly prepared from 1,2,2-trifluoro-1-trifluoromethyl-ethane sulfonic acid-containing silica gel (sample III). It was prepared following the same procedure as that used to prepare sample II and contained ˜1 mmol·g−: it was obtained by successive treatment with 4 mL of toluene and of SOCl2 (3 mL, 25 mmol), at 100° C. during 6 h, then evacuation under vacuum during 4 h. After cooling, the solid was suspended in toluene (25 mL) under argon and trifluoromethylsulfonamide (1 g, 6.7 mmol, corresponding to 5 eq. vs sulfonyl chloride loading) was poured into the reaction mixture, then triethylamine (0.8 mL, corresponding to ˜5 eq vs sulfonyl chloride loading) was injected with a syringe. The reaction mixture was heated at 90° C. under stirring during 16 h. After cooling, the solid was filtered, washed with toluene (50 mL, 3 times), washed with toluene, methanol: water mixture (60:40), ethanol, ether, then with a refluxing dichloromethane: ethyl ether mixture (50:50) using a soxhlet apparatus. The solid was washed twice with pentane (30 mL) and dried under vacuum.
In a first step, lithium hexamethyldisilazide was prepared by reaction of BuLi (2.5 mL, 0.3 10−2 mol) in anhydrous THF (35 mL) with hexamethyldisilazane (0.65 mL, 0.3 10−2 mol) at a temperature of −70° C. under argon. The temperature was gently increased to −30° C. The solution was then poured dropwise into a stirred suspension of freshly activated N-[(trifluoromethyl)sulfonyl]-(1,2,2-trifluoro-1-trifluoromethyl-ethane) sulfonamide-containing silica gel (1.5 g; 0.3 10−3 mol of sulfonamide) in anhydrous THF (35 mL) at a temperature of 0° C. Then the temperature was allowed to return gently to room temperature and the reaction mixture was stirred during 1 h.
Then, a solution of trityl chloride (0.32 g, 1.2 mmol) in THF (20 mL) was added to the reaction mixture that was stirred at room temperature during 16 h. The solid so obtained was filtered, under argon, then washed with anhydrous THF (twice with 30 mL), toluene (twice with 30 mL) then with pentane (twice with 30 mL), then evacuated under vacuum at room temperature during 4 h.
The same procedure was applied to the passivated N-[(trifluoromethyl)sulfonyl]-(1,2,2-trifluoro-1-trifluoromethyl-ethane) sulfonamide-containing silica gel in order to prepare the passivated trityl N-[(trifluoromethyl)sulfonyl]-(1,2,2-trifluoro-1-trifluoromethyl-ethane) sulfonimide-containing silica.
A sample of non-passivated lithium N-[(trifluoromethyl)sulfonyl]-(1,2,2-trifluoro-1-trifluoromethyl-ethane) sulfonimide-containing silica (1.7 g) was suspended in THF (20 mL). Then a solution 1-methyl-3-(3-triethoxysilyl)-propylimidazolium chloride (0.35 g, 1.12 mmol) was poured under argon into the suspension. The reaction mixture was refluxed for 16 h to undergo a condensation reaction of the silylated imidazolium derivatives on the residual silanols. The ionic liquid-supported silica was then filtered, then washed with (20 mL, twice), methanol:eau (2:1) mixture (20 mL, twice) in order to dissolve the lithium chloride salts, then with methanol 100%, then with a mixture of dichloromethane: diethyl ether in a Soxhlet apparatus. The solid was washed twice with pentane (30 mL) and dried under vacuum.
The supported ionic liquids and activating supports prepared in the examples hereabove were used to polymerise ethylene under the following conditions:
Solvent: 20 mL of heptane
Scavenger: 1 mL of triisobutylaluminium (TIBAL)
Pressure: 15 bars of ethylene
Polymerisation time: 30 minutes
Stirring was carried out at 1000 rpm
Metallocene catalyst component: a fresh solution of a dimethylated metallocene catalyst component sold by Total Petrochemicals under the name Z12Hsm®.
Activating support: 10 mg of 1,2,2-trifluoro-1-trifluoromethyl-ethane sulfonic acid-containing silica gel, passivated.
Ratio metallocene/activating support: 1.08.
Polyethylene was obtained with a productivity of 63 g/g/h and an activity of 0.34 kg/mmol/h. The morphology was good.
| Number | Date | Country | Kind |
|---|---|---|---|
| 07291284.3 | Oct 2007 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2008/063211 | 10/2/2008 | WO | 00 | 9/24/2010 |
