Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F17/00—Metallocenes
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
  • C07F5/06—Aluminium compounds
• • 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
  • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
  • C08F10/04—Monomers containing three or four carbon atoms
  • C08F10/08—Butenes
• • 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

Definitions

• the present invention relates to a class of bridged bis indenyl metallocene compounds having C 2 symmetry, wherein the indenyl moieties are in particular substituted in position 4 by a phenyl moiety and in positions 5 and 6 by a condensed ring, the present invention further relates to the catalyst system thereof and the polymerization process therefrom.
• Metallocene compounds are well known in the art as catalyst components for the polymerization of olefins.
• WO 03/050131 relates to a class of bis indenyl metallocene compounds wherein the indenyl moieties are at least substituted in position 4 and 5. However WO 03/050131 does not report that the substituents on positions 5 and 6 can form a condensed ring.
• PCT/EP03/12236 relates to a bis indenyl metallocene compound substituted at least in positions 2 5 and 6, wherein the substituents in positions 5 and 6 form a condensed ring.
• the substituent in position 4 is defined only in a generic way and in the compounds exemplified in the examples it is always a hydrogen atom.
• PCT/EP2004/013827 a class of bis indenyl metallocene compounds wherein the indenyl moieties are substituted in position 5 and 6 by a condensed ring is disclosed.
• PCT/EP2004/013827 is mainly focused on C 1 symmetric structures and there are no explicit disclosures of C 2 symmetric compounds. In other words this document is focused on metallocene compounds comprising two cyclopentadienyl moieties having different substitution pattern.
• An object of the present invention is a bridged metallocene compound of formula (I)
• M is an atom of a transition metal selected from those belonging to group 3, 4, or to the lanthanide or actinide groups in the Periodic Table of the Elements; preferably M is zirconium, titanium or hafnium;
• X is a hydrogen atom, a halogen atom, a R, OR,
• R is a linear or branched, cyclic or acyclic, C 1 -C 40 -alkyl, C 2 -C 40 alkenyl, C 2 -C 40 alkynyl, C 6 -C 40 -aryl, C 7 -C 40 -alkylaryl or
• R' is a Q-C ⁇ -alkylidene, C 6 -C 20 -arylidene,
• X is a hydrogen atom, a halogen atom, a OR'O or R group; more preferably X is chlorine or a methyl radical;
• L is a divalent bridging group selected from C 1 -C 20 alkylidene, C 3 -C 20 cycloalkylidene, C 6 -
• R 1 is a linear C 1 -C 40 hydrocarbon radical optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements such as methyl or ethyl radical or an alpha branched aryl or arylalkyl radical containing from 2 to 20 carbon atoms optionally containing O, N, S, P and Se atoms, in particular O, N and S atoms such as 2(5 -Me- thiophenyl) or 2(5-Me-furanyl) radicals; preferably R 1 is a linear Q-C ⁇ -alkyl, C 2 -C 40 alkenyl, C 2 -C 40 alkynyl radical, optionally containing heteroatoms belonging to groups 13- 17 of the Periodic Table of the Elements; preferably R 1 is a linear Ci-Qo-alkyl radical; more preferably R 1 is a methyl, or ethyl radical;
• R 2 and R 3 are part of 4-7 membered ring condensed to the benzene ring of the indenyl moiety; preferably a 5 or 6 membered ring; said ring optionally containing heteroatoms belonging to groups 13-16 of the Periodic Table of the Elements preferably groups 15-16 of the Periodic Table of the Elements; the valence of each atom forming said ring being substituted with R 18 radicals; that means that is filled with R 18 groups, wherein R 18 , equal to or different from each other, are hydrogen atoms or a C 1 -C 40 hydrocarbon radical; preferably R 18 is a hydrogen atom or a linear or branched, cyclic or acyclic, Ci-Gr ⁇ -alkyl, C 2 -C 40 al kenyl, C 2 -C 40 alkynyl, C 6 -C 40 -aryl, C 7 -C 40 -alkylaryl or C 7 -C 40 -arylalkyl radical, optional
• R 4 is a hydrogen atom or a C 1 -C 40 hydrocarbon radical optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably R 4 is a hydrogen atom or a linear or branched, cyclic or acyclic, Ci-Gr ⁇ -alkyl, C 2 -C 40 alkenyl, C 2 -C 40 alkynyl, C 6 -C 40 -aryl, C 7 -C 40 -alkylaryl or C 7 -C 40 -arylalkyl radical optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably R 4 is a hydrogen atom a Ci-Cio-alkyl or a C 6 -C 40 -aryl radical;
• W is an aromatic 5 or 6 membered ring that can contain heteroatoms belonging to groups 15-16 of the Periodic Table of the Elements; the valence of each atom of said ring is substituted with hydrogen atom or it can optionally be substituted with R 5 groups, wherein R 5 , equal to or different from each other, are C 1 -C 40 hydrocarbon radicals optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably R 5 , are linear or branched, cyclic or acyclic, Ci-Gr ⁇ -alkyl, C 2 -C 40 alkenyl, C 2 -C 40 alkynyl, C 6 -C 40 -aryl, C 7 -C 40 -alkylaryl or C 7 -C 40 -arylalkyl radicals optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements;
• W is selected from the group comprising the following moieties of formula (Wa), (Wb) and (Wc):
• R 6 , R 7 , R 8 , R 9 and R 10 are hydrogen atoms or C 1 - C 40 hydrocarbon radicals optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably R 6 , R 7 , R 8 , R 9 and R 10 , are hydrogen atoms or linear or branched, cyclic or acyclic, C 1 -C 40 -alkyl, C 2 -C 40 alkenyl, C 2 -C 40 alkynyl , C 6 -C 40 -aryl, C 7 -C 40 -alkylaryl or C 7 -C 40 -arylalkyl radicals optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements;
• Z 1 is a nitrogen atom or a CR 10 group
• Z 2 is a nitrogen atom or a CR 6 group
• Z 3 is a nitrogen atom or a CR 7 group
• Z 4 is a nitrogen atom or a CR 8 group
• Z 5 is a nitrogen atom or a CR 9 group; provided that not more that 2 groups among Z 1 , Z 2 , Z 3 , Z 4 and Z 5 are nitrogen atoms, preferably not more that one group among Z 1 , Z 2 , Z 3 , Z 4 and Z 5 is a nitrogen atom
• Z 6 is an oxygen atom, a sulfur atom, a NR 13 group or a CR 13 group
• Z 7 is an oxygen atom, a sulfur atom, a NR 14 group or a CR 14 group
• Z 8 is an oxygen atom, a sulfur atom, a NR 15 group or a CR 15 group
• Z 9 is an oxygen atom, a sulfur atom, a NR 16
• R 13 , R 14 , R 15 and R 16 are hydrogen atoms or C 1 -C 40 hydrocarbon radicals optionally containing heteroatoms belonging to groups 13-17 of the
• Periodic Table of the Elements preferably R 6 , R 7 , R 8 , R 9 and R 10 , are hydrogen atoms or linear or branched, cyclic or acyclic, Ci-Gr ⁇ -alkyl, C 2 -C 40 alkenyl, C 2 -C 40 alkynyl ,
• R 8 , R 9 and R 10 are hydrogen atoms, Ci-Gr ⁇ -alkyl or C 6 -C 40 -aryl radicals;
• R 7 is a C i-Gr ⁇ -alkyl radical, preferably a branched Ci-Gr ⁇ -alkyl radical such as a tertbutyl radical, more preferably R 7 is a branched Ci-Gr ⁇ -alkyl radical wherein the carbon atom in position alpha is a tertiary carbon atom and R 6 , R 8 , R 9 and R 10 are hydrogen atoms;
• R 10 and R 8 are Ci-Gr ⁇ -alkyl radicals, preferably they are linear C 1 -C 4O aI lCyI radicals such as methyl radicals and R 7 , R 8 and R 9 are hydrogen radicals:
• R 6 , R 7 and R 8 are linear or branched Ci-Gr ⁇ -alkyl radicals such as methyl or tertbutyl radicals and R 10 and R 9 are hydrogen atoms.
• R 6 , R 7 , R 8 , R 9 and R 10 are hydrogen atoms
• Z 1 is a nitrogen atom and Z 2 ,
• Z 3 , Z 4 and Z 5 are respectively CR 6 , CR 7 , CR 8 and CR 9 wherein the meaning of R 6 , R 7 , R 8 , and R 9 is described above; in a further preferred embodiment Z 3 is a nitrogen atom and
• Z 1 . Z 2 , Z 4 and Z 5 are respectively CR 10 , CR 6 , CR 8 and CR 9 wherein the meaning of R 10 ,
• R 6 , R 8 , and R 9 is described above; in a further preferred embodiment Z 2 is a nitrogen atom and Z 1 , Z 3 , Z 4 and Z 5 are respectively CR 10 , CR 7 , CR 8 and CR 9 wherein the meaning of R 10 , R 7 , R 8 , and R 9 is described above;
• Z 6 is an oxygen atom, a sulfur atom, a NR 16 group; preferably it is a sulfur atom or a NR 16 ; wherein R 16 is preferably a
• Ci-Gr ⁇ -alkyl radical more preferably Z 6 is a sulfur atom; and Z 7 , Z 8 , Z 9 and Z 10 are respectively a CR 14 , CR 15 , CR 16 and a carbon atom, wherein R 14 is a hydrogen atom or a
• Ci-Gr ⁇ -alkyl radical such as methyl or ethyl
• R 15 and R 16 are hydrogen atoms or
• Ci-Gr ⁇ -alkyl radicals Ci-Gr ⁇ -alkyl radicals.
• Examples of compounds having formula (I) are as follows Me 2 Si(6-Me-4-Ph-l,2,3,5-tetrahydro-5'-indacen-7-yl)2ZrCl2,
• a preferred class of the compounds of formula (I) is represented by formula (II):
• R 11 and R 12 are hydrogen atoms or C 1 -C 40 hydrocarbon radicals optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably R 11 and R 12 are hydrogen atoms or linear or branched, cyclic or acyclic, Ci-Gr ⁇ -alkyl, C 2 -C 40 alkenyl, C 2 -C 40 alkynyl radicals, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; more preferably R 11 and R 12 are hydrogen atoms or Ci-Cio-alkyl radical s such as methyl or ethyl radicals.
• a further preferred class of compounds of formula (I) has formula (Ha)
• the metallocene compounds object of the present invention have the meaning reported above.
• the two cyclopentadienyl moieties have the same substitution patterns That means that the two indenyl moieties bounded on the central metal atom are substituted in the same way, or in other words, the substituents R 1 , R 2 , R 3 , R 4 and W are the same on each indenyl moiety.
• the metallocene compounds of formula (I) have C 2 symmetry. Metallocene symmetry classes can be found on Resconi et al. Chemical Reviews, 2000, Vol. 100, No. 4 1263 and references herein cited.
• metallocene compounds object of the present invention are in their racemic(rac) form.
• a further object of the present invention is a catalyst system for the polymerization of olefin obtainable by contacting: a) a metallocene compound of formula (I); b) at least an alumoxane or a compound able to form an alkylmetallocene cation; and c) optionally an organo aluminum compound.
• the metallocene compounds have formula (II) or (Ha).
• Alumoxanes used as component b) in the catalyst system according to the present invention can be obtained by reacting water with an organo-aluminium compound of formula H j AlU 3- J or H j AyJ 6- J, where the U substituents, same or different, are hydrogen atoms, halogen atoms, Ci-Cio-alkyl, C 3 -C2 0 -cyclalkyl, C 6 -C2o-aryl, C 7 -C2o-alkylaryl or C 7 -C2o-arylalkyl radicals, optionally containing silicon or germanium atoms, with the proviso that at least one U is different from halogen, and j ranges from 0 to 1, being also a non- integer number.
• organo-aluminium compound of formula H j AlU 3- J or H j AyJ 6- J where the U substituents, same or different, are hydrogen atoms, halogen atoms, Ci-Cio-alky
• the molar ratio of Al/water is preferably comprised between 1 : 1 and 100: 1.
• the alumoxanes used in the catalyst system according to the invention are considered to be linear, branched or cyclic compounds containing at least one group of the type:
• n 1 is 0 or an integer of from 1 to 40 and the substituents U are defined as above; or alumoxanes of the formula:
• (Al — O)n 2 can be used in the case of cyclic compounds, wherein n 2 is an integer from 2 to 40 and the U substituents are defined as above.
• alumoxanes suitable for use according to the present invention are methylalumoxane (MAO), tetra-(isobutyl)alumoxane (TIBAO), tetra-(2,4,4-trimethyl- pentyl)alumoxane (TIOAO), tetra-(2,3-dimethylbutyl)alumoxane (TDMBAO) and tetra-
• TTMBAO (2,3,3-trimethylbutyl)alumoxane
• Non-limiting examples of aluminium compounds that can be reacted with water to give suitable alumoxanes (b), described in WO 99/21899 and WO01/21674, are: tris(2,3,3-trimethyl-butyl)aluminium, tris(2,3-dimethyl-hexyl)aluminium, tris(2,3-dimethyl- butyl)aluminium, tris(2,3-dimethyl-pentyl)aluminium, tris(2,3-dimethyl-heptyl)aluminium, tris(2-methyl-3-ethyl-pentyl)aluminium, tris(2-methyl-3-ethyl-hexyl)aluminium, tris(2-methyl-3 -ethyl-heptyl)aluminium, tris(2-methyl-3 -propyl-hexyl)aluminium, tris(2-ethyl-3-methyl-butyl)aluminium
• trimethylaluminium TMA
• triisobutylaluminium TIBA
• tris(2,4,4-trimethyl-pentyl)aluminium TIOA
• tris(2,3- dimethylbutyl)aluminium TDMBA
• tris(2,3,3-trimethylbutyl)aluminium TTMBA
• Non-limiting examples of compounds able to form an alkylmetallocene cation are compounds of formula D + E " , wherein D + is a Br ⁇ nsted acid, able to donate a proton and to react irreversibly with a substituent X of the metallocene of formula (I) and E " is a compatible anion, which is able to stabilize the active catalytic species originating from the reaction of the two compounds, and which is sufficiently labile to be removed by an olefinic monomer.
• the anion E " comprises one or more boron atoms.
• the anion E " is an anion of the formula BAr 4 ( ) , wherein the substituents Ar which can be identical or different are aryl radicals such as phenyl, pentafluorophenyl or bis(trifluoromethyl)phenyl. Tetrakis-pentafluorophenyl borate is particularly preferred compound, as described in WO 91/02012.
• compounds of formula BAr 3 can be conveniently used. Compounds of this type are described, for example, in the International patent application WO 92/00333. Other examples of compounds able to form an alkylmetallocene cation are compounds of formula BAr 3 P wherein P is a substituted or unsubstituted pyrrol radical. These compounds are described in WO01/62764. Compounds containing boron atoms can be conveniently supported according to the description of DE-A-
• Non limiting examples of compounds of formula D + E " are:
• Triphenylphosphoniumtetrakis(phenyl)borate Triethylphosphoniumtetrakis(phenyl)borate
• Triphenylcarbeniumtetrakis(pentafluorophenyl)borate Triphenylcarbeniumtetrakis(pentafluorophenyl)borate
• Organic aluminum compounds used as compound c) are those of formula H j AlU 3- J or
• the catalysts of the present invention can also be supported on an inert carrier. This is achieved by depositing the metallocene compound a) or the product of the reaction thereof with the component b), or the component b) and then the metallocene compound a) on an inert support.
• the support can be a porous solid such as talc, a sheet silicate, an inorganic oxide or a finely divided polymer powder (e.g. polyolefin). Suitable inorganic oxides may be found among the oxides of elements of groups 2, 3, 4, 5, 13, 14, 15 and 16 of the
• oxides preferred as supports include silicon dioxide, aluminum oxide, and also mixed oxides of the elements calcium, aluminum, silicon, magnesium or titanium and also corresponding oxide mixtures, magnesium halides, styrene/divinylbenzene copolymers, polyethylene or polypropylene.
• oxides preferred as supports include silicon dioxide, aluminum oxide, and also mixed oxides of the elements calcium, aluminum, silicon, magnesium or titanium and also corresponding oxide mixtures, magnesium halides, styrene/divinylbenzene copolymers, polyethylene or polypropylene.
• Other inorganic oxides which can be used alone or in combination with the abovementioned preferred oxidic supports are, for example, MgO, ZrO 2 , TiO 2 or B 2 O 3 .
• a suitable class of supports which can be used is that constituted by porous organic supports functionalized with groups having active hydrogen atoms. Particularly suitable are those in which the organic support is a partially crosslinked styrene polymer. Supports of this type are described in European application EP-633 272.
• inert supports particularly suitable for use according to the invention is that of polyolefin porous prepolymers, particularly polyethylene.
• a further suitable class of inert supports for use according to the invention is that of porous magnesium halides such as those described in International application WO 95/32995.
• the support materials used preferably have a specific surface area in the range from 10 to 1 000 m 2 /g, a pore volume in the range from 0.1 to 5 ml/g and a mean particle size of from 1 to 500 ⁇ m.
• the inorganic support can be subjected to a thermal treatment, e.g. to remove adsorbed water.
• Such a drying treatment is generally carried out at from 80 to 300°C, preferably from 100 to 200°C, with drying at from 100 to 200°C preferably being carried out under reduced pressure and/or a blanket of inert gas (e.g. nitrogen), or the inorganic support can be calcined at from 200 to 1 000°C to produce the desired structure of the solid and/or set the desired OH concentration on the surface.
• the support can also be treated chemically using customary desiccants such as metal alkyls, preferably aluminum alkyls, chlorosilanes or SiCl 4 , or else methylaluminoxane. Appropriate treatment methods are described, for example, in WO 00/31090.
• the inorganic support material can also be chemically modified.
• treatment of silica gel with (NH 4 )2SiF 6 leads to fluorination of the silica gel surface
• treatment of silica gels with silanes containing nitrogen-, fluorine- or sulfur-containing groups leads to correspondingly modified silica gel surfaces.
• Organic support materials such as finely divided polyolefin powders (e.g. polyethylene, polypropylene or polystyrene) can also be used and are preferably likewise freed of adhering moisture, solvent residues or other impurities by means of appropriate purification and drying operations before use. It is also possible to use functionalized polymer supports, e.g. supports based on polystyrene, via whose functional groups, for example ammonium or hydroxy groups, at least one of the catalyst components can be immobilized.
• functionalized polymer supports e.g. supports based on polystyrene, via whose functional groups, for example ammonium or hydroxy groups, at least one of the catalyst components can be immobilized.
• the solid compound obtained by supporting the catalyst system object of the present invention on a carrier in combination with the further addition of the alkylaluminium compound either as such or prereacted with water if necessary, can be usefully employed in the gas-phase or slurry polymerization.
• a further object of the present invention is a catalyst system as described above, further comprising d) an inert carrier.
• the metallocene compounds of formula (I) object of the present invention are particularly suitable for the homo and copolymerization of propylene.
• the metallocene-based catalyst system of the present invention when used for homo or copolymerizing propylene are able to give polymers having a high molecular weight in high yields also at high temperatures rendering thus possible to use it in the industrial plants that use polymerization temperatures higher than 50°C and that can be comprised between 60 and
• the content of alpha-olefins derived units in the propylene copolymer object of the present invention ranges from 0.1 to 90% by mol; preferably it ranges from 5% by mol to
• the metallocene compounds of the present invention are also particularly suitable for the preparation of copolymers of ethylene and higher alpha olefins, such as propylene, 1- butene, 1-hexene, 1-octene.
• the copolymers have a comonomer content ranging from 5 to 50% by mol.
• Particularly preferred are ethylene/1 -butene copolymer having a content of 1 -butene derive units ranging from 5 to 50% by mol.
• Said copolymers can be obtained in high yields by using a gas phase process such a fluidized bed or stirred bed reactor.
• the process for the polymerization of olefins according to the invention can be carried out in slurry or in the gas phase.
• the hydrocarbon solvent can either be aromatic such as toluene, or aliphatic such as propane, hexane, heptane, or isobutane.
• the polymerization temperature is generally comprised between -100°C and +200°C and, particularly between 10°C and +100°C.
• the polymerization pressure is generally comprised between 0,5 and 100 bar.
• the polymerization yields depend on the purity of the metallocene compound.
• the metallocene compounds obtained by the process of the invention can therefore be used as such or can be subjected to purification treatments.
• the amount of hydrogen ranges from 0.5 NL (normal liter) to 10 NL; even more preferably it ranges from 4.5 NL to 8 NL.
• the catalyst system based on the metallocene compounds object of the present invention can be used in a multistage process for preparing heterophasic propylene copolymers.
• step a) further comprises a prepolymerization step a-1).
• Said hydrocarbon solvent can be either aromatic (such as toluene) or aliphatic (such as propane, hexane, heptane, isobutane, cyclohexane and 2,2,4-trimethylpentane).
• the polymerization medium is liquid propylene.
• Step a) can be carried out in the presence of hydrogen.
• the amount of hydrogen present during the polymerization reaction is preferably more than 1 ppm; more preferably from 5 to 2000 ppm; even more preferably from 6 to 500 ppm with respect to the propylene present in the reactor.
• Hydrogen can be added either at the beginning of the polymerization reaction or it can also be added at a later stage after a prepolymerization step has been carried out.
• Preferred comonomers are ethylene or 1-butene.
• a propylene homopolymer is produced.
• the content of the polymer obtained in step a) preferably ranges from 5% to 90% by weight of the polymer produced in the whole process, more preferably it ranges from 10% to 70% by weight and still more preferably from 25% to 65% by weight of the total polymer produced in the whole process.
• step b) is carried out in a gas phase, preferably in a fluidized or stirred bed reactor.
• the polymerization temperature is generally comprised between -100°C and +200°C, and, preferably, between 10°C and +90°C.
• the polymerization pressure is generally comprised between 0,5 and 100 bar.
• Preferred comonomers are ethylene or 1-butene.
• the content of polymer obtained in step b) preferably ranges from 10 to 95% by weight of the polymer produced in the whole process, preferably it ranges from 30% to 90% by weight and more preferably from 35% to 75% by weight.
• the polymer obtained in step b) can optionally contains up to 20% by mol of a non conjugated diene.
• Non conjugated dienes can be a straight chain, branched chain or cyclic hydrocarbon diene having from 6 to 20 carbon atoms. Examples of suitable non- conjugated dienes are:
• branched chain acyclic dienes such as 5-methyl- 1,4-hexadiene, 3, 7 -dimethyl- 1,6- octadiene, 3,7-dimethyl-l,7-octadiene and mixed isomers of dihydro myricene and dihydroocinene;
• - single ring alicyclic dienes such as 1,3-cyclopentadiene, 1,4-cyclohexadiene, 1,5- cyclooctadiene and 1,5-cyclododecadiene;
• - multi-ring alicyclic fused and bridged ring dienes such as tetrahydroindene, methyl tetrahydroindene, dicyclopentadiene, bicyclo-(2,2,l)-hepta-2, 5 -diene; and
• alkenyl, alkylidene, cycloalkenyl and cycloalkylidene norbornenes such as 5- methylene-2-norbornene (MNB), 5-propenyl-2-norbornene, 5-isopropylidene-2- norbornene,5 -(4-cyclopentenyl)-2-norbornene, 5 -cyclohexylidene-2-norbornene, 5 - vinyl-2-norbornene and norbornadiene.
• Preferred dienes are 1,4-hexadiene (HD), 5-ethylidene-2-norbornene (ENB), 5- vinylidene-2-norbornene (VNB), 5-methylene-2-norbornene (MNB) and dicyclopentadiene (DCPD). Particularly preferred dienes are 5-ethylidene-2-norbornene
• non-conjugated dienes are preferably incorporated into the polymer in an amount from 0.1% to about 20% by mol, preferably from 0.5% to 15% by mol, and more preferably from 0.5% to 7% by mol. If desired, more than one diene may be incorporated simultaneously, for example HD and ENB, with total diene incorporation within the limits specified above.
• step al) further comprises a prepolymerization step al-1).
• Said hydrocarbon solvent can be either aromatic (such as toluene) or aliphatic (such as propane, hexane, heptane, isobutane, cyclohexane and 2,2,4-trimethylpentane).
• Step al) can be carried out in the presence of hydrogen.
• the amount of hydrogen present during the polymerization reaction is preferably more than 1 ppm; more preferably from 5 to 2000 ppm; even more preferably from 6 to 500 ppm with respect to the propylene present in the reactor. Hydrogen can be added either at the beginning of the polymerization reaction or it can also be added at a later stage after a prepolymerization step has been carried out.
• Preferred comonomers are ethylene or 1-butene.
• a propylene homopolymer is produced.
• the content of the polymer obtained in step al) preferably ranges from 5% to 90% by weight of the polymer produced in the whole process, more preferably it ranges from 10% to 70% by weight and still more preferably from 25% to 65% by weight of the total polymer produced in the whole process.
• step bl) is carried out in a gas phase, preferably in a fluidized or stirred bed reactor.
• the polymerization temperature is generally comprised between -100°C and +200°C, and, preferably, between 10°C and +90°C.
• the polymerization pressure is generally comprised between 0,5 and 100 bar.
• Preferred comonomers are propylene or 1-butene.
• the content of polymer obtained in step bl) preferably ranges from 10 to 95% by weight of the polymer produced in the whole process, preferably it ranges from 30% to 90% by weight and more preferably from 35% to 75% by weight.
• the polymer obtained in step bl) can optionally contains up to 20% by mol of a non conjugated diene.
• Non conjugated dienes can be a straight chain, branched chain or cyclic hydrocarbon diene having from 6 to 20 carbon atoms. Examples of suitable non- conjugated dienes are:
• branched chain acyclic dienes such as 5-methyl- 1,4-hexadiene, 3, 7 -dimethyl- 1,6- octadiene, 3,7-dimethyl-l,7-octadiene and mixed isomers of dihydro myricene and dihydroocinene;
• - single ring alicyclic dienes such as 1,3-cyclopentadiene, 1,4-cyclohexadiene, 1,5- cyclooctadiene and 1,5-cyclododecadiene;
• - multi-ring alicyclic fused and bridged ring dienes such as tetrahydroindene, methyl tetrahydroindene, dicyclopentadiene, bicyclo-(2,2,l)-hepta-2, 5 -diene; and
• alkenyl, alkylidene, cycloalkenyl and cycloalkylidene norbornenes such as 5- methylene-2-norbornene (MNB), 5-propenyl-2-norbornene, 5-isopropylidene-2- norbornene,5 -(4-cyclopentenyl)-2-norbornene, 5 -cyclohexylidene-2-norbornene, 5 - vinyl-2-norbornene and norbornadiene.
• Preferred dienes are 1,4-hexadiene (HD), 5-ethylidene-2-norbornene (ENB), 5- vinylidene-2-norbornene (VNB), 5-methylene-2-norbornene (MNB) and dicyclopentadiene (DCPD). Particularly preferred dienes are 5-ethylidene-2-norbornene
• non-conjugated dienes are preferably incorporated into the polymer in an amount from 0.1% to about 20% by mol, preferably from 0.5% to 15% by mol, and more preferably from 0.5% to 7% by mol. If desired, more than one diene may be incorporated simultaneously, for example HD and ENB, with total diene incorporation within the limits specified above.
• the processes of the present invention can be carried out in one reactor or in two or more reactors in series.
• a further preferred ligand has formula (HIb)
• the metallocene compounds of formula (I) can be obtained with a process comprising the steps of reacting the dianion with a suitable transition metal source such as metal tetrahalide as for example zirconium tetrachloride.
• a suitable transition metal source such as metal tetrahalide as for example zirconium tetrachloride.
• the dianion can be obtained for example by the deprotonation of the ligand of formula (III), for example by using an organolithium compound such as buthyl or methyl lithium.
• the ligand of formula (III) can be easily prepared starting from the cyclopentadienyl moiety of formula (IV)
• the process described above can be carried out also "one pot" by reacting a calculate amount of the compound of formula LY 2 with the dianionic derivative formed in step a).
• the above processes are preferably carried out in an aprotic solvent, either polar or apolar.
• Said aprotic solvent is preferably an aromatic or aliphatic hydrocarbon, optionally halogenated, or an ether; more preferably it is selected from benzene, toluene, pentane, hexane, heptane, cyclohexane, dichloromethane, diethylether, tetrahydrofurane and mixtures thereof.
• the above process is carried out at a temperature ranging from -100°C to +80°C, more preferably from -20°C to +70°C.
• examples 1 -5 were done in tetrahydronaphthalene (THN) solution obtained by dissolving the polymer at 135°C for 1 hour as described above.
• TBN tetrahydronaphthalene
• DSC Mettler The instrument is calibrated with indium and tin standards.
• the weighted sample (5-10 mg), was sealed into aluminum pans, heated to 200°C and kept at that temperature for a time long enough (5 minutes) to allow a complete melting of all the crystallites. Successively, after cooling at 20°C/min to 0°C and standing for 5 minutes at
• the sample was heated to 200°C at a rate of 20°C/min.
• the peak temperature was assumed as melting temperature (T m ) and the area as the global melting enthalpy ( ⁇ H).
• Mass average molar masses (Mw) and number average molar masses (Mn) of the polymers were determined.
• Methylalumoxane was received from Albemarle as a 30% wt/V toluene solution and used as such and the silica was received from ESfEOS ( ES70Y, ioo microns).
• the support is suspended in 20 ml toluene, then brought to 80°C, and stirred for 30 min at this temperature before hot filtration.
• the MAO/silica is suspended at 15 °C in 20 ml toluene.
• a solution of 0.25 mmol (207 mg, 40 ⁇ mol/g carrier) of the metallocene indicated in table 1 in 2 ml MAO and 2 ml toluene is slowly added.
• the reaction mixture is stirred for 1 h at 15 °C, and after raising the temperature to 40 °C, again stirred for 2 h. Then, it is filtered.
• Prepolymerization 252 g propylene are fed in the autoclave at 0°C.
• the catalytic system is injected in the reactor and propylene is prepolymerized at 30°C for 5 minutes.
• the reactor temperature was raised from 30 to 70°C (in 10 minutes).
• 59 cc H 2 are fed, corresponding to 2.63 mmol H 2 .
• Propylene polymerization in bulk this step is carried out at 30 bar-g pressure and 70°C until the liquid propylene is totally consumed, and the pressure inside the reactor starts to decrease.
• the resulting polymer has been subjected to xylene extraction at 25°C according to the procedure described above.
• the fraction of polymer soluble in xylene at 25°C has been taken as the amount of ethylene propylene copolymers produced in the process.
• the polymerization data are reported in table 1
• Prepolymerization 134 g propylene are fed in the autoclave at 0°C.
• the catalytic system is injected in the reactor and propylene is prepolymerized at 30°C for 5 minutes.
• the reactor temperature was raised from 30 to 80°C (in 10 minutes).
• Propylene polymerization in gas phase this step is carried out at 21 bar-g pressure and 80°C until 70 grams of propylene are consumed and the pressure inside the reactor starts to decrease.
• the PP matrix polymerization time is recorded and the pressure is released down to 0.1 bar-g propylene; at the same time the temperature decreases to 30°C.
• Step b) In examples 4-6 the procedure used in examples 1 -3 has been repeated excepting that the Ethylene propylene molar ratio (ethylene(C2)/propylene(C3)+ethylene(C2)) fed was 0.2 and the polymerization in step b) was stopped when 232 grams of monomers were consumed. The results are reported in table 2
• a metallocene dichloride (A-I) were added at room temperature to 4.33mmol of MAO (30% strength solution in toluene, from Albemarle). The solution was allowed to stand overnight at room temperature and was subsequently diluted with 10.9ml of toluene. The diluted solution was carefully added to 1Og of silica (Sylopol 948, calcined at 600°C, from Grace). Particular attention was paid to the colored solution being uniformly distributed over the support material. After 10 minutes, the flask containing the catalyst suspension was connected to a vacuum line and dried until the content of volatile material had been reduced to less than 5% by weight. Propylene homopolymerization
• Homopolymerizations were carried out in a 10 1 reactor charged with 3.5kg of liquid propene.
• the reactor was made inert by means of nitrogen before being charged.
• 8ml of a 20% strength by weight solution of triethylaluminum in Exxsol (from Witco) were introduced into the reactor and the mixture was stirred at 30°C for 15 minutes.
• a suspension of the respective catalyst as indicated in table 3 in 20ml of Exxsol was introduced into the reactor.
• the reactor temperature was increased to 65 °C and maintained at this temperature for 60 minutes.
• the polymerizations were stopped by venting the reactor.
• the polymers were dried overnight under reduced pressure before being analyzed.
• TIBA Triisobutylaluminum
• the autoclave is filled with 550 g Propylene and 70 mg Hydrogen.
• the catalytic system obtained as described above (the metallocene used is A-I amounts indicated in table 4) is injected in the reactor by using additional 150 g liquid propylene,.
• the temperature is increased at 40°C, in 2-3 minutes, and the propylene is polymerized at this temperature for 5 minutes.
• the monomer is totally flashed out.
• the reactor is filled with the fresh Ethylene/Propylene monomer mixture and the t emperature is increased to 60°C in order to reach the desired polymerization pressure (21 barg). This step needs about 10 minutes.
• Step c) The ethylene/propylene mixture is fed at constant pressure for 60 minutes. Then the reactor is vented and cooled down to room temperature; thus, the reaction is stopped. The polymer is collected and dried at reduced pressure and 60°C.
• the catalyst system was prepared according to example 6 above by using A-I. Propylene homopolymerization
• Homopolymerizations were carried out in a 10 1 reactor charged with 3.5kg of liquid propene and an hydrogen amount as indicated in table 5.
• the reactor was made inert by means of nitrogen before being charged.
• 8ml of a 20% strength by weight solution of triethylaluminum in Exxsol (from Witco) were introduced into the reactor and the mixture was stirred at 30°C for 15 minutes.
• An amount indicated in table 5 of the catalyst system in suspension of 20ml of Exxsol was introduced into the reactor.
• the reactor temperature was increased to 65 °C and maintained at this temperature for 60 minutes.
• the polymerizations were stopped by venting the reactor.
• the polymers were dried overnight under reduced pressure before being analyzed.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
• Catalysts (AREA)

Priority Applications (9)

Applications Claiming Priority (2)

Publications (1)

Family

ID=36228814

Family Applications (1)

Country Status (14)

Cited By (166)

Families Citing this family (16)

Citations (2)

Family Cites Families (49)

• 2006
  • 2006-03-15 RU RU2007138560/04A patent/RU2410388C2/ru active
  • 2006-03-15 BR BRPI0611557A patent/BRPI0611557B1/pt active IP Right Grant
  • 2006-03-15 AU AU2006224576A patent/AU2006224576B2/en not_active Ceased
  • 2006-03-15 ES ES06708781T patent/ES2316050T3/es active Active
  • 2006-03-15 DE DE602006003194T patent/DE602006003194D1/de active Active
  • 2006-03-15 EP EP06708781A patent/EP1858907B1/en active Active
  • 2006-03-15 CN CN2006800087032A patent/CN101142224B/zh active Active
  • 2006-03-15 AT AT06708781T patent/ATE411330T1/de not_active IP Right Cessation
  • 2006-03-15 WO PCT/EP2006/060767 patent/WO2006097497A1/en not_active Ceased
  • 2006-03-15 KR KR1020077021417A patent/KR101293405B1/ko active Active
  • 2006-03-15 JP JP2008501307A patent/JP5075113B2/ja active Active
  • 2006-03-15 US US11/886,646 patent/US7842764B2/en active Active
  • 2006-03-15 PL PL06708781T patent/PL1858907T3/pl unknown
• 2007
  • 2007-08-24 ZA ZA200707189A patent/ZA200707189B/xx unknown

Patent Citations (2)

Also Published As

Similar Documents

Legal Events