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EP1613674A1 - Systemes de catalyseurs ziegler-natta et leurs procedes de preparation - Google Patents

Systemes de catalyseurs ziegler-natta et leurs procedes de preparation

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Publication number
EP1613674A1
EP1613674A1 EP04727239A EP04727239A EP1613674A1 EP 1613674 A1 EP1613674 A1 EP 1613674A1 EP 04727239 A EP04727239 A EP 04727239A EP 04727239 A EP04727239 A EP 04727239A EP 1613674 A1 EP1613674 A1 EP 1613674A1
Authority
EP
European Patent Office
Prior art keywords
polymerization
compound
catalyst systems
olefins
magnesium
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04727239A
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German (de)
English (en)
Inventor
Klaus Foettinger
Martin Schneider
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Basell Poliolefine Italia SRL
Original Assignee
Basell Poliolefine Italia SRL
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE10317395A external-priority patent/DE10317395A1/de
Application filed by Basell Poliolefine Italia SRL filed Critical Basell Poliolefine Italia SRL
Publication of EP1613674A1 publication Critical patent/EP1613674A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00—Polymerisation catalysts
    • C08F4/02—Carriers therefor
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F110/02—Ethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00—Polymerisation catalysts
    • C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62—Refractory metals or compounds thereof
    • C08F4/63—Pretreating the metal or compound covered by group C08F4/62 before the final contacting with the metal or compound covered by group C08F4/44
    • C08F4/632—Pretreating with metals or metal-containing compounds
    • C08F4/634—Pretreating with metals or metal-containing compounds with magnesium or compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00—Polymerisation catalysts
    • C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62—Refractory metals or compounds thereof
    • C08F4/64—Titanium, zirconium, hafnium or compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers

Definitions

  • the present invention relates to catalyst systems of the Ziegler-Natta type, to a process for preparing them and to their use for the polymerization of olefins.
  • Catalyst systems of the Ziegler-Natta type have been known for a long time. These systems are used, in particular, for the polymerization of C 2 -C 10 -alk-1-enes and comprise, inter alia, compounds of polyvalent titanium, aluminum halides and/or aluminum alkyls together with a suitable support material.
  • the preparation of the Ziegler-Natta catalysts usually occurs in two steps. The titanium-containing solid component is prepared first and is subsequently reacted with the co- catalyst. The polymerization is subsequently carried out using the catalysts obtained in this way.
  • a magnesium compound is usually applied to the support first and the titanium component is added in a later step. Such a process is disclosed, for exam- pie, in EP-A-594915.
  • EP-A- 014523 describes, for example, a process for preparing Ziegler catalysts, in which an inorganic oxide is reacted in any order with a magnesium alkyl and a halogenating reagent and the resulting intermediate is reacted in any order with a Lewis base and titanium tetrachloride. This catalyst can then be used together with an aluminum alkyl and further Lewis bases for the polymerization of olefins.
  • WO 99/46306 discloses a process for preparing Ziegler-Natta catalysts in which a silica gel is silylated, subsequently brought into contact with a titanium compound and the intermediate ob- tained in this way is reacted with an alkyl magnesium alkoxide. Lewis bases are not used.
  • a further process for preparing Ziegler-Natta catalysts is disclosed in EP-A-027733, in which an oxidic support material is brought into contact with a titanium compound, the intermediate obtained in this way is reacted with an alkyl magnesium compound, and a reagent selected from the group consisting of hydrogen chloride, hydrogen bromide, water, acetic acid, alcohols, carboxylic acids, phosphorus pentachloride, silicon tetrachloride, acetylene and mixtures thereof is subsequently added. No further Lewis bases are used here either.
  • the comonomer incorporation behavior of various catalyst systems is indicated at a constant ratio of ethylene to comonomer in the reactor by the formation of copoly- mers having a relatively low density.
  • the copolymers formed should have a low content of extractable material, especially in the low density range.
  • Copolymers which have been prepared by means of a Ziegler catalyst usually display, especially at densities in the range from 0.91 to 0.93 g/cm 3 , quite high proportions of extractable, i.e. low molecular weight, material.
  • step B) bringing the intermediate obtained from step A) into contact with a magnesium compound MgR 1 n X 1 2 -n, where X 1 are each, independently of one another, fluorine, chlorine, bromine, iodine, hydrogen, NR X 2> OR x , SR X , S0 3 R x or OC(0)R x , and R 1 and R x are each, independently of one another, a linear, branched or cyclic CrC 2 o-alkyl, a C 2 -C 10 -alkenyl, an alkylaryl having 1-10 carbon atoms in the alkyl part and 6-20 carbon atoms in the aryl part or a C 6 - C 18 -aryl and n is 1 or 2,
  • step C) bringing the intermediate obtained from step B) into contact with a halogenating reagent
  • step D) bringing the intermediate obtained from step C) into contact with a donor compound.
  • the invention further provides catalyst systems of the Ziegler-Natta type which can be prepared by the process of the present invention, prepolymerized catalyst systems and a process for the polymerization or copolymerization of olefins at from 20 to 150°C and pressures of from 1 to 100 bar, wherein the polymerization or copolymerization is carried out in the presence of at last one catalyst system according to the present invention and, if appropriate, an aluminum compound as cocatalyst.
  • catalyst systems of the Ziegler-Natta type which can be prepared by the process of the present invention, prepolymerized catalyst systems and a process for the polymerization or copolymerization of olefins at from 20 to 150°C and pressures of from 1 to 100 bar, wherein the polymerization or copolymerization is carried out in the presence of at last one catalyst system according to the present invention and, if appropriate, an aluminum compound as cocatalyst.
  • inorganic metal oxide use is made of, for example, silica gel, aluminum oxide, hydrotalcite, mesoporous materials and aluminosilicate, in particular silica gel.
  • the inorganic metal oxide can have been partially or fully modified prior to the reaction in step A).
  • the support material can, for example, be treated at from 100 to 1000°C under oxidizing or non- oxidizing conditions, if desired in the presence of fluorinating agents such as ammonium hexafluorosilicate.
  • fluorinating agents such as ammonium hexafluorosilicate.
  • the water and/or OH group content for example, can be varied in this way.
  • the support material is preferably dried under reduced pressure at from 100 to 800°C, preferably from 150 to 650°C, for from 1 to 10 hours before being used in the process of the present inven- tion. If the inorganic metal oxide is silica, this is not reacted with an organosilane prior to step A).
  • the inorganic metal oxide has a mean particle diameter of from 5 to 200 ⁇ m, preferably from 10 to 100 ⁇ m and particularly preferably from 20 to 70 ⁇ , an average pore volume of from 0.1 to 10 ml/g, in particular from 0.8 to 4.0 ml/g and particularly preferably from 0.8 to 2.5 ml/g, and a specific surface area of from 10 to 1000 m 2 /g, in particular from 50 to 900 m 2 /g, particularly preferably from 100 to 600 m 2 /g.
  • the inorganic metal oxide can be spherical or granular and is preferably spherical.
  • the specific surface area and the mean pore volume are determined by nitrogen adsorption using the BET method, as described, for example, in S. Brunauer, P. Emmett and E. Teller in Journal of the American Chemical Society, 60, (1939), pages 209-319.
  • spray-dried silica gel is used as inorganic metal oxide.
  • the primary particles of the spray-dried silica gel have a mean particle diameter of from 1 to 10 ⁇ m, in particular from 1 to 5 ⁇ m.
  • the primary particles are porous, granular silica gel particles which are obtained from an Si0 2 hydrogel by milling, if necessary after appropriate sieving.
  • the spray-dried silica gel can then be produced by spray drying the primary particles slurried with water or an aliphatic alcohol.
  • such a silica gel is also commercially available.
  • the spray- dried silica gel which can be obtained in this way has voids or channels which have a mean diameter of from 1 to 10 ⁇ m, in particular from 1 to 5 ⁇ m, and whose macroscopic proportion by • volume in the total particle is in the range from 5 to 20%, in particular in the range from 5 to 15%.
  • These voids or channels usually have a positive influence on the diffusion-controlled access of monomers and cocatalysts and thus also on the polymerization kinetics.
  • the inorganic metal oxide is firstly reacted with a tetravalent titanium compound in step A).
  • a tetravalent titanium compound in step A, use is generally made of compounds of tetravalent titanium of the formula (R 3 0) t X .,Ti, where the radical R 3 is as defined for R and X 2 is as defined for X above and t is from 0 to 4.
  • tetraalkoxytitanium such as tetramethoxytitanium, tetraethoxytitanium, tetrapropoxytitanium, tetraisopropoxytitanium, tetrabutoxytitanium or tita- nium(IV)-2-ethylhexoxide, trialkoxytitanium halides (t equals 3 and X 2 equals halide) such as titanium chloride triisopropoxide and titanium tetrahalides (t equals 0, X 2 equals halogen).
  • X 2 is chlorine or bromine, particularly preferably chlorine.
  • Very particular preference is given to using titanium tetrachloride.
  • Step A) can be carried out in any aprotic solvent.
  • Particularly useful solvents are aliphatic and aromatic hydrocarbons in which the titanium compound is soluble, e.g. pentane, hexane, heptane, octane, dodecane, a benzene or a C 7 -C 10 -alkyIben ⁇ ene such as toluene, xylene or ethylbenzene.
  • a particularly preferred solvent is ethylbenzene.
  • the inorganic metal oxide is usually slurried in the aliphatic or aromatic hydrocarbon, and the titanium compound is added thereto.
  • the titanium compound can be added as a pure substance or as a solution in an aliphatic or aromatic hydrocarbon, preferably pentane, hexane, heptane or toluene. However, it is also possible for example, to add the solution of the organometallic com- pound to the dry inorganic metal oxide.
  • the titanium compound is preferably mixed with the solvent and subsequently added to the suspended inorganic metal oxide.
  • the titanium compound is preferably soluble in the solvent.
  • Reaction step A) can be carried out at from 0 to 150 °C, preferably from 20 to 80°C.
  • the amount of titanium compound used is usually selected so as to be in the range from 0.1 to 20 mmol, preferably from 0.5 to 15 mmol and particularly preferably from 1 to 10 mmol, per gram of inorganic metal oxide.
  • step A it is also possible to add only part of the titanium compound, e.g. from 50 to 99% by weight of the total amount of the titanium compound to be used, in step A) and to add the remainder in one or more of the further steps. Preference is given to adding the total amount of the organometallic compound in step A).
  • step B) the intermediate obtained from step A) is, usually without work-up or isolation, reacted with the magnesium compound MgR 1 n X 1 2 - n>
  • X 1 are each, independently of one another, fluorine, chlorine, bromine, iodine, hydrogen, R x , NR X 2 , OR , SR X , S0 3 R x or OC(0)R x
  • R 1 and R x are each, independently of one another, a linear, branched or cyclic CrC 2 o alkyl, a C 2 -C ⁇ 0 - alkenyl, an alkylaryl having 1-10 carbon atoms in the alkyl part and 6-20 carbon atoms in the aryl part or a C 6 -C 18 -aryl and n is from 1 to 2.
  • Mixtures of individual magnesium compounds MgR n X 1 2n can also be used as magnesium compound MgR 1 n X 1 2 . n .
  • X 1 is as defined above for X.
  • X 1 is preferably chlorine, bromine, methoxy, ethpxy, isopropoxy, butoxy or acetate.
  • R 1 and R x are as defined above for R.
  • R 1 are each, independently of one another, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl * sec-pentyl, isopentyl, n-hexyl, n-heptyl, n-octyl, benzyl, o-, m-, p-methylbenzyl, 1- or 2-ethylpheny), phenyl or 1-naphthyl.
  • Possible magnesium compounds are, in particular, alkylmagnesium halides, magnesium alkyls and magnesium aryls and also magnesium alkoxide and- alkylmagnesium aryloxide compounds, with preference being given to using d C ⁇ ⁇ o-alky magnesium compounds, in particular di(C r C 1D -alkyl)magnesi ⁇ m compounds.
  • magnesium compounds MgR 1 2 e.g. di- methylmagnesium, diethylmagnesium, dibutylmagnesium, dibenzylmagnesium, (bu- tyl)(ethyl)magnesium or (butyl)(octyl)magnesium.
  • Suitable solvents for step B) are the same ones as for step A).
  • Aliphatic and aromatic hydrocarbons in which the magnesium compound is soluble e.g. pentane, hexane, heptane, octane, iso- octane, nonane, dodecane, cyclohexane, benzene or a C 7 -C 10 -alkylbenzene such as toluene, xylene or ethylbenzene, are particularly useful.
  • a particularly preferred solvent is heptane.
  • the intermediate obtained from step A) is usually slurried in the aliphatic and/or aromatic hydrocarbon, and the magnesium compound is added thereto.
  • the magnesium compound can be added as a pure substance or, preferably, as a solution in an aliphatic or aromatic hydrocarbon such as pentane, hexane, heptane or toluene. However, it is also possible to add the solution of the magnesium compound to the intermediate obtained from step A).
  • the reaction is usually carried out at from 0 to 150 C C, preferably from 30 to 120°C and particularly preferably from 40 to 100°C.
  • the magnesium compound is usually used in an amount of from 0.1 to 20 mmol, preferably from 0.5 to 15 mmol and particularly preferably from 1 to 10 mmol, per gram of inorganic metal oxide.
  • the molar ratio of titanium compound used to magnesium compound used is in the range from 10:1 to 1 :20, preferably from 1 :1 to 1 :3 and particularly preferably from 1 :1.1 to 1 :2.
  • the intermediate obtained from reaction step B) is, preferably without intermediate isolation, reacted with the halogenating reagent in step C).
  • Possible halogenating reagents are compounds which can halogenate the magnesium compound used, e.g. hydrogen halides such as HF, HCI, HBr and HJ, silicon halides such as tetrachlorosi- lane, trichloromethylsilane, dichlorodimethylsilane or trimethylchlorosilane, carbbxylic acid halides such as acetyl chloride, formyl chloride or propionyl chloride, boron halides, phosphorus penta- chloride, thionyl chloride, sulfuryl chloride, phosgene, nitrosyl chloride, mineral acid halides, chlorine, bromine, chlorinated polysiloxanes, alkylaluminum chloride, aluminum trichloride, ammonium hexafluorosilicate and alkyl halide compounds of the formula R y s -C-Y 4 .
  • hydrogen halides such as HF
  • R ⁇ is hydrogen or a linear, branched or cyclic C C 2 o-alkyl such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl or n-dodecyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl or cyclododecyl, where the radicals R ⁇ are also able to be substituted by chlorine or bromine, Y is chlorine or bromine, and s is 0, 1 , 2
  • Halogenating reagents such as titanium tetrahalides, for example titanium tetrachlorides, are not very suitable. Preference is given to using a chlorinating reagent.
  • Preferred halogenating reagents are alkyl halide compounds of the formula R Y S -C-CI 4 . S such as methyl chloride, ethyl chloride, n-propyl chloride, n-butyl chloride, tert-butyl chloride, di- chloromethane, chloroform or carbon tetrachloride.
  • alkyl halide compounds of the formula R Y -C-CI 3 in which R ⁇ is preferably hydrogen, methyl, ethyl, n- propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl or n-hexyl.
  • R ⁇ is preferably hydrogen, methyl, ethyl, n- propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl or n-hexyl.
  • R ⁇ is preferably hydrogen, methyl, ethyl, n- propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl,
  • Suitable solvents for the reaction with the halogenating reagent are in principle the same ones as those for step A).
  • the reaction is usually carried out at from 0 to 200°C and preferably from 20 to 120°C.
  • the molar ratio of halogenating reagent used to magnesium compounds used is in the range from 4:1 to 0.05:1 , preferably from 3:1 to 0.5:1 and particularly preferably from 2:1 to 1 :1.
  • the magnesium compound can be partly or fully halogenated in this way.
  • the magnesium compound is preferably fully halogenated.
  • the intermediate obtained from step C) is usually reacted without intermediate isolation with one or more donor compounds, preferably one donor compound.
  • Suitable donor compounds possess at least one atom of Group 15 and/or 16 of the Periodic Table of the Elements, for example monofunctional or polyfunctional carboxylic acids, carboxylic anhydrides and carboxylic esters, also ketones, ethers, alcohols, lactones and organophosphorus and organosilicon compounds.
  • a donor compound which contains at least one nitrogen atom, preferably one nitrogen atom, for example monofunctional or polyfunctional carboxamides, amino acids, ureas, imines or amines.
  • Preference is given to using one nitrogen- containing compound or a mixture of a plurality of nitrogen-containing compounds.
  • R 4 and R 5 are each, independently of one another, linear, branched or cyclic C-j-C 2 o-alkyl such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl, n-hexyl, n-heptyl, n-octyl, n-n ⁇ nyl, n-decyl or n- dodecyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl or cyclododecyl, C 2 -C 2 o-alkenyl, which
  • R 4 and R 5 may also be joined to form a 5- or 6-membered ring and the organic radicals R 4 and R 5 may also bear halogens such as fluorine, chlorine or bromine as sub- stituents, or SiR 6 3 .
  • R can also be hydrogen. Preference is given to amines in which one R 4 is hydrogen.
  • organosilicon radicals SiR 6 3 possible radicals R 6 are the same radicals as have been described in detail above for R 5 , where two R 6 may also be joined to form a 5- or 6- membered ring.
  • organosilicon radicals are trimethylsilyl, triethylsilyl, butyldi- methylsilyl, tributylsilyl, triallylsilyl, triphenylsilyl and dimethylphenylsilyl.
  • R 6 is a linear, branched or cyclic C-rCaralkyl such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl or n-dodecyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl; cyclooctyl, cyclononyl or cyclododecyl.
  • Very particular preference is given to hexamethyldisil
  • R 7 and R 8 are each a linear, branched or cyclic CrCzo-alkyl such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl or n-dodecyl, cyclopropane, cyciobutane, cyclopentane, cyclohexane, cyclohep- tane, cyclooctane, cyclononane or cyclododecane, C 2 -C 20 -alkenyl, which
  • R 7 may also be hydrogen.
  • Possible radicals R 9 in organosilicon radicals SiR 9 3 are the same radicals which have been mentioned above for R 7 , and it is also possible for two R 7 to be joined to form a 5- or 6- membered ring.
  • suitable organosilicon radicals are trimethylsilyl, triethylsilyl, butyldi- methylsilyl, tributylsilyl, triallylsilyl, triphenylsilyl and dimethylphenylsilyl.
  • carboxylic esters R 7 r C0-0R 8 in which R 7 and R s are each a linear or branched C 1 -C 8 -alkyl such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert- butyl, n-pentyl, sec-pentyl, isopentyl, n-hexyl, n-heptyl or n-octyl.
  • R 7 and R s are each a linear or branched C 1 -C 8 -alkyl such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert- butyl, n-pentyl, sec-pentyl, isopentyl, n-hexyl, n-heptyl or
  • acetic esters in particular C-rC 6 -alkyl acetates such as methyl acetate,” ethyl acetate, propyl acetate or isopropyl acetate.
  • the carboxylic esters give catalysts which exhibit high productivities, especially in the gas phase.
  • Suitable solvents for the reaction with the donor compound are the same ones as for step A).
  • Aliphatic and aromatic hydrocarbons such as pentane, hexane, heptane, octane, dodecane, a benzene or a C 7 -C 10 -alkylbenzene such as toluene, xylene or ethylbenzene are particularly useful.
  • a particularly preferred solvent is ethylbenzene.
  • the donor compound is preferably soluble in the solvent.
  • the reaction is usually carried out at from 0 to 150°C, preferably from 0 to 100°C and particularly preferably from 20 to 70°C.
  • the intermediate obtained from step C) is usually slurried in a solvent and the donor compound is added thereto. However, it is also possible, for example, to dissolve the donor compound in the solvent and subsequently to add it to the intermediate obtained from step C).
  • the donor com- pound is preferably soluble in the solvent.
  • the molar ratio of titanium compound used to donor compound used is generally in the range from 1 :100 to 1 :0.05, preferably from 1 :10 to 1 :0.1 and particularly preferably from 1 :1 to 1 :0.4.
  • the catalyst obtained from step D) or a variant thereof which has been m ' odified further can optionally be reacted with further reagents, for example, with an alcohol of the formula R 2 -OH, where R 2 is a linear, branched or cyclic C ⁇ -C 20 -alkyl, a C 2 -C 10 -alkenyl, an alkylaryl having 1-10 carbon atoms in the alkyl part and 6-20 carbon atoms in the aryl part or a C 6 -C ⁇ 8 -aryl, and/or an organometallic compound of an element of Group 3 of the Periodic Table.
  • R 2 is a linear, branched or cyclic C ⁇ -C 20 -alkyl, a C 2 -C 10 -alkenyl, an alkylaryl having 1-10 carbon atoms in the alkyl part and 6-20 carbon atoms in the aryl part or a C 6 -C ⁇ 8 -aryl, and/or an organ
  • Suitable alcohols are, for example, methanol, ethanol, 1-propanol, 2-propa ⁇ ol, 1-butanol, 2- butanol, 1-pentanol, 2-pentanol, 1-hexanol, 2-ethylhexanol, 2,2-dimethylethanol or 2,2-dimethyl- propanol, in particular ethanol, 1-propanol, 1-butanol, 1-pentanol, 1-hexanol or 2-ethylhexanol.
  • Suitable solvents for the reaction with alcohol are the same ones as for step A).
  • the reaction is usually carried out at from 0 to 150°C, preferably from 20 to 100°C and particularly preferably from 60 to 100°C.
  • the molar ratio of alcohol used to magnesium compound used is usually in the range from 0.01 :1 to 20:1 , preferably .from 0.05:1 to 10:1 and particularly preferably from 0.1 :1 to 1 :1.
  • the catalyst obtained from step D) or its reaction product with other reagents can also be brought into contact with an organometallic compound MRmXs-m of a metal of Group 3 of the Periodic Table of the Elements, where X are each, independently of one another, fluorine, chlorine, bromine, iodine, hydrogen, NR x 2 , OR x , SR X , S0 3 R x or OC(0)R x , and R and R x are each, independently of one another, a linear, branched or cyclic, C C 20 -alkyl, a C 2 -C ⁇ 0 -alkenyl, an alkylaryl having 1-10 carbon atoms in the alkyl part and 6-20 carbon atoms in the aryl part or a C 6 - C 18 -aryl, M is a metal of Group 3 of the Periodic Table, preferably B, Al or Ga and particularly preferably Al, and m is 1 , 2 or 3.
  • X are
  • R are each, independently of one another, a linear, branched or cyclic C ⁇ -C 20 -alkyl such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl or n-dodecyl, cyclopropyl, cyclobutyl, cyclo- pentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl or cyclododecyl, a C 2 -C 10 -alkenyl, which may be linear, cyclic or branched and in which the double bond can be internal
  • alkylaryl having 1-10 carbon atoms in the alkyl part and 6-20 carbon atoms in the aryl part, e.g. benzyl, o-, m-, p-methylbenzyl, 1- or 2-ethylphenyi, or a C 6 -C 18 -aryl which may bear further alkyl groups as substituents, e.g.
  • phenyl 1-naphthyl, 2-na ' phthyl, 1-a ⁇ thryl, 2- anthryl, 9-a ⁇ thryl, 1-phenanthryl, 2-phenanthryI, 3-phenanthryl, 4-phenanthryl and 9-phenanthryl, 2-biphenyl, o-, m-, p-methylphenyl, 2,3-, 2,4-, 2,5-, or 2,6-dimethylphenyl, 2,3,4-, 2,3,5-, 2,3,6-, 2,4,5-, 2,4,6- or 3,4,5-trimethylphenyl, where two R may also be joined to form a 5- or 6- membered ring and the organic radicals R may also be substituted by halogens such as fluorine, chlorine, or bromine.
  • halogens such as fluorine, chlorine, or bromine.
  • X are each, independently of one another, fluorine, chlorine, bromine, iodine, hydrogen, amide NR x 2 , alkoxide OR x , thiolate SR X , sulfonate S0 3 R or carboxylate OC(0)R x , where R x is as defined for R.
  • NR X 2 can be, for example, dimethylamino, diethylamino or diisopropylamino
  • OR x can be methoxy, ethoxy, isopropoxy, butoxy, hexoxy, or 2-ethylhexoxy
  • S0 3 R x can be methylsul- fonate, trifluoromethylsulfonate or toluenesulfonate
  • OC(0)R x can be formate, acetate or propionate.
  • organometallic compound of an element of Group 3 of the Periodic Table preference is given to using an aluminum compound AIR ⁇ -m, where the variables are as defined above.
  • suitable compounds are trialkylaluminum compounds such as trimethylalu inum, triethylalumi- num, triisobutylaluminum or tributylaluminum, dialkylaluminum halides such as dimethylaluminum chloride, diethylaluminum chloride or dimethylaluminum fluoride, alkylaluminum dihalides such as methylaluminum dichloride or ethylaluminum dichloride, or mixtures such as methylaluminur ⁇ sesquichloride.
  • the reaction products of aluminum alkyls with alcohols can also be used.
  • Preferred aluminum compounds are those in which X is chlorine.
  • X is chlorine
  • m is 2.
  • Suitable solvents for the reaction with the organometallic compound MR ⁇ -m of a metal of Group 3 of the Periodic Table of the Elements are the same ones as for step A).
  • Aliphatic and aromatic hydrocarbons in which the organometallic compound of an element of Group 3 of the Periodic Table is soluble e.g. pentane, hexane, heptane, octane, dodecane, a benzene, or a C 7 -C ⁇ 0 - alkylbenzene such as toluene, xylene or ethylbenzene, are particularly useful.
  • a particularly preferred solvent is ethylbenzene.
  • the reaction is usually carried out at from 20 to 150°C, preferably from 40 to 100°C. If an organometallic compound of a metal of Group 3 of the Periodic Table of the Elements is employed in the formulation, it is usually used in an amount of from 0.005 to 100 mmol, preferably from 0.05 to 5 mmol and particularly preferably from 0.1 to 1 mmol, per gram of inorganic metal oxide.
  • the catalyst system or an intermediate obtained in this way can be washed one or more times with an aliphatic or aromatic hydrocarbon such as pentane, hexane, heptane, octane, nonane, decane, dodecane, cyclohexane, benzene or a C 7 -C 10 -alkylbenzene such as toluene, xylene or ethylbenzene.
  • an aliphatic or aromatic hydrocarbon such as pentane, hexane, heptane, octane, nonane, decane, dodecane, cyclohexane, benzene or a C 7 -C 10 -alkylbenzene such as toluene, xylene or ethylbenzene.
  • aliphatic hydrocarbons in particular pentane, n-hexane or isohexane, n-
  • This is usually carried out at from 0 to 200°C, preferably from 0 to 150°C and particularly preferably from 20 to 100°C, for from 1 minute to 20 hours, preferably from 10 minutes to 10 hours and particularly preferably from 30 minutes to 5 hours.
  • the catalyst is stirred with the solvent and then filtered off. This step can be repeated once or twice.
  • the catalyst can also be washed by extraction, e.g. in a Soxhlett apparatus, which achieves continuous washing.
  • Step D) or the optional reactions or the last washing step is preferably followed by a drying step in which all or part of the residual solvent is removed.
  • the novel catalyst system obtained in this way can be completely dry or have a certain residual moisture content.
  • the amount of volatile constituents should be not more than 20% by weight, in particular not more than 10% by weight, based on the catalyst system.
  • the novel catalyst system obtainable in this way or its preferred embodiments advantageously has/have a titanium content of from 0.1 to 30% by weight, preferably from 0.5 to 10% by weight and particularly preferably from 0 ' .7 to 3% by weight, and a magnesium content of from 0.1 to 30% by weight, preferably from 0.5 to 20% by weight and particularly preferably from 0.8 to 6% by weight.
  • an olefin preferably an ⁇ -olefin, for example vinyl cyclohexane, styrene or phenyldimethylvinylsilane
  • an antistatic or a suitable inert compound such as a wax or oil
  • the molarratio of additives to transition metal compound B) is usually from 1 :1000 to 1000:1 , preferably from 1 :5 to 20:1.
  • the process for the polymerization or copolymerization of olefins in the presence of at least one catalyst system according to the present invention and, if appropriate, an aluminum compound as cocatalyst is carried out at from 20 to 150°C and pressures of from 1 to 100 bar.
  • the process of the invention for the polymerization of olefins can be combined with all industrially known polymerization processes at from 20 to 150°C and under pressures of from 1 to 100 bar, in particular from 5 to 50 bar.
  • the advantageous pressure and temperature ranges for carrying out the process therefore depend greatly on the polymerization method.
  • the catalyst systems used according to the present invention can be employed in all known polymerization processes, in a known manner in bulk, in suspension, in the gas phase or in a supercritical medium in the customary reactors used for the polymerization of olefins, for example in suspension polymeriza- tion processes, in solution polymerization processes, in stirred gas-phase processes or in gas- phase fluidized-bed processes.
  • the process can be carried out batchwise or preferably continuously in one or more stages. '
  • gas-phase polymerization in particular in gas- phase fluidized bed reactors, solution polymerization and suspension polymerization, in particular in loop reactors and stirred tank reactors, are preferred.
  • the suitable gas-phase fluidized-bed processes are described in detail in, for example, EP-A-004645, EP-A-089691 , EP-A-120503 or EP-A-241947.
  • the gas-phase polymerization can also be carried out in the condensed or super- condensed mode in which part of the circulating gas is cooled to below the dew point and re- turned as a two-phase mixture to the reactor. It is also possible to use a reactor having two or more polymerization zones.
  • the two polymerization zones are linked to one another and the polymer is alternately passed through these two zones a plurality of times, with the two zones also being able to have different polymerization conditions.
  • a reactor is described, for example, in WO 97/04015.
  • Different or even identical polymerization processes can also, if desired, be connected in series so as to form a polymerization cascade, for example as in the Hostalen process. It is also possible to carry out two or more identical or different processes in parallel reactors.
  • the Ziegler catalysts of the present invention can also be carried out by means of combinatorial methods or be tested for polymerization activity with the aid of these combinatorial methods.
  • the molar mass of the polyalk-1-enes formed in this way can be controlled and adjusted over a wide range by addition of regulators customary in polymerization technology, for example hydrogen. Furthermore, further customary additives such as antistatics can also be used in the polym- erizations. In addition, the product output can be varied via the amount of Ziegler catalyst metered in.
  • the (co)polymers produced can then be conveyed to a deodorization or deactivation vessel in which they can be subjected to a customary and known treatment with nitrogen and/or steam.
  • the temperature set is generally at least a few degrees below the softened temperature of the polymer. In particular, temperatures in the range from 50 to 150°C, preferably from 70 to 120°C, are set in these polymerization processes.
  • the polymerization is usually carried out in a suspension medium, preferably in an inert hydrocarbon such as isobutane, or else in the monomers themselves.
  • the polymerization temperatures are generally in the range from 20 to 115°C
  • the pressure is generally in the range from 1 to 100 bar, in particular from 5 to 40 bar.
  • the solids content of the suspension is generally in the range from 10 to 80%.
  • olefinically unsaturated compounds can be polymerized by the process of the present invention; for the purposes of the invention, the term polymerization encompasses copolymeriza- tion.
  • Possible olefins include ethylene and linear or branched ⁇ -olefins having from 3 to 12 carbon atoms, e.g.
  • propene 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, 1-nonene, 1-decene, 1-dodecene or 4-methyl- 1-pentene, and also nonconjugated and conjugated dienes such as a butadiene, 1 ,5-hexadiene or 1 ,6-heptadiene, cyclic olefins such as cyclohexene, cyclopentene or norbornene and polar monomers such as acrylic esters, acrylamides, acrolein, acrylonitrile, ester or amide derivatives of methacrylic acid, vinyl ethers, allyl ethers and vinyl acetate.
  • dienes such as a butadiene, 1 ,5-hexadiene or 1 ,6-heptadiene, cyclic olefins such as cyclohexene, cyclopentene or norbornene
  • Vinyl aromatic compounds such as styrene can also be polymerized by the process of the present invention. Preference is given to polymerizing at least one ⁇ -olefin selected from the group consisting of ethene, propene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene and 1-decene, in particular ethene. Mixtures of three or more ole- fins can also be copolymerized.
  • ethylene is polymerized or ethylene is copolymerized with C 3 -C 8 - ⁇ -monoolefins, in particular ethylene with C 3 -C 8 - ⁇ -olefins.
  • ethylene is copolymerized together with an ⁇ -olefin selected from the group consisting of propene, 1-butene, 1-pentene, 1-hexene, 1-heptene and 1-octene.
  • Aluminum compounds suitable as cocatalyst are, in particular, compounds of the formula AlR 7 m X 3 3 .m > where R 7 is as defined above for R and X 3 is as defined above for X and m is 1 , 2 or 3.
  • compounds in which one or two alkyl groups have been replaced by alkoxy groups in particular d-Cio-dialkylaluminum alkoxides such as diethylaluminum ethoxide, or by one or two halogen atoms, for example chlorine or bromine, in particular dimethylaluminum chloride, methylaluminum dichloride, methylaluminum sesquechlo- ride or diethylaluminum chloride, are useful as cocatalysts.
  • trialkyla- luminum compounds whose alkyl groups each have from 1 to 15 carbon atoms, for example tri- methylaluminum, methyldiethylaluminum, triethylaluminum, triisobutylaluminum, tributylaluminum, trihexylaluminum or trioctylaluminum.
  • cocatalysts of the aluminoxane type in particular methylaluminoxane MAO.
  • Aluminoxanes are prepared, for example, by controlled addition of water to alkylaluminum compounds, in particular trimethylaluminum.
  • Aluminox- ane preparations suitable as cocatalyst are commercially available.
  • the amount of aluminum compounds to be used depends on their effectiveness as cocatalysts. Since many of the cocatalysts are simultaneously used for the removal of catalyst poisons (scavengers), the amount used depends on the level of contamination of the other starting materials. However, a person skilled in the art can determine the optimum amount by simple experimentation.
  • the cocatalyst is preferably used in such an amount that the atomic ratio of aluminum from the aluminum compound used as cocatalyst and titanium from the catalyst system of the present invention is from 10:1 to 800:1 , in particular from 20:1 to 200:1.
  • the various aluminum compounds can be used as cocatalyst either individually or as a mixture of two or more components in any order.
  • these aluminum compounds serving as cocatalysts can be allowed to act on the catalyst systems of the present invention either in succession or together.
  • the catalyst system of the present invention can be brought into contact with the cocatalyst or cocatalysts either before or after it is brought into contact with the olefins to be polym- erized.
  • Preactivation using one or more cocatalysts prior to mixing with the olefin and further addition of the same or other cocatalysts after the preactivated mixture has been brought into contact with the olefin is also possible.
  • Preactivation is usually carried out at from 0 to 150°C, in particular from 20 to 80°C, and pressures of from 1 to 100 bar, in particular from 1 to 40 bar.
  • the catalyst systems of the present invention can also be used in combination with at least one catalyst customary for the polymerization of olefins.
  • Possible catalysts here are, in particular, Phillips catalysts based on chromium oxides, metallocenes (e.g. EP-A- 29368), constrained geometry complexes (e.g. EP-A-0416815 or EP-A-0420436), nickel and palladium bisimine systems (for preparation of these, see WO-A-98/03559), iron and cobalt pyridinebisimine compounds (for preparation of these, see WO-A-98/27124) or chromium amides (cf. for example, 95JP-170947).
  • catalysts are metallocenes having at least one ligand based on a cyclopentadienyl or heterocyclodienyl having a fused-on heterocycle, where the heterocycles are preferably aromatic and contain nitrogen and/or sulfur. Such compounds are described, for example, in WO 98/22486. Further suitable catalysts are substituted monocyclopentadienyl, monoindenyl, monofluorenyl or heterocyclopentadienyl complexes of chromium in which at least one of the substituents on the cyclopentadienyl ring bears a donor function.
  • a further cocatalyst whose addition enables the catalysts to be active in the olefin polymerization.
  • These are preferably cation-forming compounds.
  • Suitable cation-forming compounds are, for example, aluminoxane-type compounds, strong uncharged Lewis acids, in particular tris(pentafluorophenyl)borane, ionic com- pounds having a Lewis-acid cation or ionic compounds containing Br ⁇ nsted acids as cations, in particular, N,N-di-methylanilinium tetrakis(pentafluorophenyl)borate and especially N,N-dimethyl- cyclohexylammoniur ⁇ tetrakis(pentafluorophenyl)borate or N,N-dimethylbenzylammonium tetrakis(pentafluorophenyl)borate.
  • the catalyst system of the present invention is preferably used in the presence of at least one catalyst customary for the polymerization of olefins and, if desired, one or more cocatalysts.
  • the catalyst customary for the polymerization of olefins can have been applied to the same inorganic metal oxide or be immobilized on another support material and be used simultaneously or in any order with the catalyst system of the present invention.
  • the process of the present invention makes it possible to prepare polymers of olefins having molar masses in the range from about 10000 to 5000000, preferably 20000 to 1000000, with polymers having molar masses (weight average) in the range from 20 000 to 400 000 being particu- larly preferred.
  • the catalyst systems of the present invention are particularly well-suited to preparing ethylene homopolymers and copolymers of ethylene with ⁇ -olefins.
  • 2 - ⁇ -olefins containing up to 10% by weight of comonomer in the copolymer can be prepared.
  • Preferred copolymers contain from 0.3 to 1.5 mol% of 1-hexene or 1- butene, based on the polymer, and particularly preferably from 0.5 to 1 mol% of 1-hexene or 1- butene.
  • the bulk densities of the ethylene homopolymers and copolymers of ethylene with ⁇ -olefins which are obtainable in this way are in the range from 240 to 590 g/l, preferably from 245 to 550 g/l.
  • ethylene homopolymers having densities of 0.95 - 0.96 g/cm 3 and copolymers of ethylene with C 4 -C 8 - ⁇ -olefins, in particular ethylene-hexene copolymers and ethylene-butene copolymers, having a density of 0.92-0.94 g/cm 3 , a polydispersity M w /M n of from 3 to 8, preferably from 4.5 to 6, can be obtained using the catalyst system of the present invention.
  • the proportion of material which can be extracted from the homopolymers and copolymers of ethylene by cold heptane is usually in the range from 0.01 to 3% by weight, preferably from 0.05 to 2% by weight, based on the ethylene polymer used.
  • the polymer prepared according to the present invention can also form mixtures with other olefin polymers, in particular homopolymers and copolymers of ethylene. These mixtures can be prepared by the above-described simultaneous polymerization over a plurality of catalysts or they can be prepared simply by subsequent blending of the polymers prepared according to the pres- ent invention with other homopolymers or copolymers of ethylene.
  • the polymers, ethylene copolymers, polymer mixtures and blends can further comprise auxiliaries and/or additives known per se, e.g. processing stabilizers, stabilizers against the action of light and heat, customary additives such as lubricants, antioxidants, antiblocking agents and antistatics, and also, if appropriate, colorants.
  • auxiliaries and/or additives known per se, e.g. processing stabilizers, stabilizers against the action of light and heat, customary additives such as lubricants, antioxidants, antiblocking agents and antistatics, and also, if appropriate, colorants.
  • additives e.g. processing stabilizers, stabilizers against the action of light and heat, customary additives such as lubricants, antioxidants, antiblocking agents and antistatics, and also, if appropriate, colorants.
  • colorants e.g., colorants, e.g., colorants, and also, if appropriate, colorants.
  • colorants e.g.
  • polymers prepared according to the present invention can also be modified subsequently by grafting, crosslinking, hydrogenation or other functionalization reactions known to those skilled in the art.
  • the polymers and copolymers of olefins, in particular homopolymers and copolymers of ethylene, prepared using the catalyst systems of the present invention are particularly suitable for the production of films, fibers and moldings.
  • the catalyst systems of the present invention are very useful for preparing homopolymers and copolymers of ethylene. They give high productivities, even at high polymerization temperatures. The polymers produced using them have high bulk densities and low contents of components that can be extracted using cold heptane. The catalysts additionally display good incorporation of comonomers and the molar masses of the polymers can readily be regulated by means of hydrogen.
  • the Staudinger index (??)[dl/g] was determined at 130°C using an automatic Ubbelohde viscome- ter (Lauda PVS 1 ) and decalin as solvent (ISO 1628 at 130°C, 0.001 g/ml of decalin).
  • the bulk density (BD) [g/l] was determined in accordance with DIN 53468.
  • the determination of the molar mass distributions and the means M n , M w and M w /M ⁇ derived therefrom was carried out by means of high-temperature gel permeation chromatography (GPC) using a method based on DIN 55672 under the following conditions: solvent: 1 ,2,4- trichlorobenzene, flow: 1 ml/min, temperature: 140°C, calibration using PE standards.
  • the cold heptane extractables were determined by stirring 10 g of the polymer powder in 50 ml of heptane at 23°C for 2 h. The polymer was filtered off from the extract obtained in this way and washed with 100 ml of heptane. The combined heptane phases were freed of the solvent and dried to constant weight. The residue is weighed and is the cold heptane extractables.
  • the particle sizes were determined by a method based on ISOWD 13320 Particle size Analysis using a Malvern Mastersi ⁇ er 2000 (Small Volume MS1 ) under an inert gas atmosphere.
  • the content of the elements magnesium and aluminum was determined on samples digested in a mixture of concentrated nitric acid, phosphoric acid and sulfuric acid using an inductively coupled plasma atomic emission spectrometer (ICP-AES) from Spectro, Kleve, Germany, by means of the spectral lines at 277.982 nm for magnesium and 309.271 nm for aluminum.
  • the titanium content was determined on samples digested in a mixture of 25% strength sulfuric acid and 30% strength hydrogen peroxide by means of the spectral line at 470 nm.
  • a first step 147 g of finely divided spray-dried silica gel ES 70X from Crossfield which had been dried at 660°C were suspended in ethylbenzene and admixed while stirring with a solution of 19- ml of titanium tetrachloride. The suspension obtained in this way was stirred at 100°C for 2 hours, cooled to room temperature, the solid was filtered off and washed twice with ethylbenzene. The solid obtained in this way was resuspended in ethylbenzene and admixed with 200.12 ml of (n-butyl) 1 . 5 (octyl)o. 5 magnesium (0.875 M in n-heptane).
  • the solid obtained in this way was filtered off, washed with heptane and dried at 60°C under reduced pressure. This gave 179.9 g of the catalyst system having a magnesium content of 2.5% by weight, an aluminum content of less than 0.1 % by weight, a chlorine content of 9.9% by weight and a titanium content of 2.0% by weight, in each case based on the finished catalyst system.
  • the solid obtained in this way was resuspended in ethylbenzene and mixed with 7.35 ml of ethyl acetate.
  • the solid obtained in this way was filtered off, washed with heptane and dried at 60°C under reduced pressure. This gave 188 g of the catalyst system having a magnesium content of 2.3% by weight, an aluminum content of less than 0.1 % by weight, a chlorine content of 10.5% by weight and a titanium content of 2.1 % by weight, in each case based on the finished catalyst system.
  • Example 3 (Comparative Example) In a first step, 51.8 g of finely divided spray-dried silica gel ES 70X from Crossfield which had been dried at 600°C were suspended in ethylbenzene and admixed while stirring with a solution of 6.86 ml of titanium tetrachloride. The suspension obtained in this way was stirred at 100°C for 2 hours, cooled to room temperature, the solid was filtered off and washed twice with ethylbenzene. The solid obtained in this way was resuspended in ethylbenzene and admixed with 72.52 ml of (n- butyl) 5 (octyl) 0 .
  • Example 4 (Comparative Example) 100.3 g of finely divided spray-dried silica gel ES 70X from Crossfield which had been dried at 600°C was suspended in ethylbenzene and admixed while stirring with a solution of 13.23 ml of titanium tetrachloride. The suspension obtained in this way was stirred at 100°C for 1.5 hours, cooled to room temperature, the solid was filtered off and washed twice with ethylbenzene.
  • the solid obtained in this way was resuspended in ethylbenzene and admixed with 137.6 ml of (n- butyl) 1 5 (octyl) 0 , 5 magnesium (0.875 M in n-heptane). This suspension was stirred at 80°C for one hour, cooled to room temperature, the solid was filtered off and washed twice with ethylbenzene. This solid was resuspended in ethylbenzene, 27.63 ml of tetrachlorosilane were added and subsequently stirred at 80°C for 1.5 hours.
  • the solid obtained in this way was filtered off, washed with heptane and dried at 60°C under reduced pressure. This gave 129.9 g of the catalyst system having a magnesium content of 2.15% by weight, an aluminum content of less than 0.1 % by weight, a chlorine content of 10.05% by weight and a titanium content of 3.1 % by weight, in each case based on the finished catalyst system.
  • the polymerizations were carried out in a 101 stirring autoclave. Under nitrogen, 1 g of TEAL (tri- ethylaluminum) together with 4 I of isobutane and 1 I of butene were introduced into the autoclave at room temperature. The autoclave was then pressurized with 4 bar of H 2 and 16 bar of ethylene, the weight of catalyst indicated in Table 1 was introduced and polymerization was carried out at an internal reactor temperature of 70°C for 1 hour. The reaction was stopped by venting. Table 1 shows the productivity of the catalyst systems from examples 1 and 4 and the density and the ⁇ value of the ethylene-butene copolymers obtained both for example 5 according to the present invention and for comparative example 6.
  • TEAL tri- ethylaluminum
  • Example 3 The catalyst from Example 3 (C) was polymerized as described in Examples 5 and 6 under the same conditions.
  • the catalyst from Example 3 gave an ethylene copolymer having a bulk density of 254 g/l and a 77 value of 1.48 dl/g.
  • Table 2 below shows the productivity of the catalysts used both for Example 8 according to the present invention and for comparative Example 9.

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Abstract

La présente invention a trait à des systèmes de catalyseurs Ziegler-Natta et un procédé pour leur préparation, à leur utilisation pour la polymérisation d'oléfines et à des copolymères d'éthylène qui peuvent être préparés au moyen du système de catalyseur de l'invention.
EP04727239A 2003-04-15 2004-04-14 Systemes de catalyseurs ziegler-natta et leurs procedes de preparation Withdrawn EP1613674A1 (fr)

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US47441503P 2003-05-30 2003-05-30
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RU2005135115A (ru) * 2003-04-15 2006-05-10 Базелль Полиолефине Итали с.р.л. (IT) Каталитические системы типа циглера-натта и способ их получения
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Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1130269A (fr) * 1979-10-19 1982-08-24 James J. Harris Procede de polymerisation d'alpha-monoolefines et catalyseurs supportes
JPS5662806A (en) * 1979-10-19 1981-05-29 Arco Polymers Inc Carried catalyst for olefin polymerization
US4530912A (en) * 1981-06-04 1985-07-23 Chemplex Company Polymerization catalyst and method
DE3229315A1 (de) * 1982-08-05 1984-02-09 Wacker-Chemie GmbH, 8000 München Verfahren zur polymerisation von (alpha)-olefinen
IT1178466B (it) * 1984-03-20 1987-09-09 Montedison Spa Catalizzatori per la omo e copolimerizzazione dell'etilene e polimeri ottenuti
JPH0774247B2 (ja) * 1987-03-27 1995-08-09 チッソ株式会社 α−オレフイン重合体を製造する方法
JPH0780968B2 (ja) * 1987-09-09 1995-08-30 住友化学工業株式会社 オレフィン重合体の製造法
US5145821A (en) * 1990-05-09 1992-09-08 Quantum Chemical Corporation Silica supported polymerization catalyst system
WO1989010942A1 (fr) * 1988-05-13 1989-11-16 Mitsui Petrochemical Industries, Ltd. Composant catalyseur a base de titane, procede de production, catalyseur permettant de produire un polymere ethylenique contenant ledit composant catalyseur a base de titane, et procede de production de ce polymere ethylenique
FI89066C (fi) * 1989-11-20 1993-08-10 Neste Oy Foerfarande foer framstaellning av en polymeriseringskatalytkomponent foer olefiner, en polymeriseringskatalytkomponent framstaelld med foerfarandet och dess bruk
FI91767C (fi) * 1990-04-12 1994-08-10 Neste Oy Olefiinien polymerointiin tarkoitettu prokatalyyttikompositio, sen valmistus ja käyttö
JPH0517522A (ja) * 1990-10-03 1993-01-26 Mitsui Petrochem Ind Ltd α−オレフイン重合体
FR2706467B1 (fr) * 1992-10-26 1995-09-15 Bp Chemicals Snc Procédé de préparation d'un catalyseur de type Ziegler-Natta et utilisation.
DE69600988T2 (de) * 1995-10-02 1999-07-08 Borealis Ag, Schwechat-Mannswoerth Trägerkatalysator für die Olefinpolymerisation
DE69717440T2 (de) * 1996-06-21 2003-10-02 W.R. Grace & Co.-Conn., New York Aggregatträger und darauf angebrachte olefinpolymerisationskatalysatoren
US6177375B1 (en) * 1998-03-09 2001-01-23 Pq Corporation High activity olefin polymerization catalysts
SG73622A1 (en) * 1998-03-11 2000-06-20 Sumitomo Chemical Co Solid catalyst component and catalyst for olefin polymerization and process for producing olefin polymer
JP3752074B2 (ja) * 1998-04-06 2006-03-08 三井化学株式会社 α−オレフィンの重合方法
DE10163075A1 (de) * 2001-12-20 2003-07-10 Basell Polyolefine Gmbh Katalysatorsysteme von Typ der Ziegler-Natta-Katalysatoren und ein Verfahren zu deren Herstellung
RU2005135115A (ru) * 2003-04-15 2006-05-10 Базелль Полиолефине Итали с.р.л. (IT) Каталитические системы типа циглера-натта и способ их получения

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
None *
See also references of WO2004092232A1 *

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WO2004092232A1 (fr) 2004-10-28
RU2005135113A (ru) 2006-05-10
KR20060012585A (ko) 2006-02-08
AR044021A1 (es) 2005-08-24
JP2006523741A (ja) 2006-10-19
BRPI0409430A (pt) 2006-04-25

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