WO2017011073A1 - Composés catalyseurs métallocènes de type bis-indényle substitué comprenant un pont -si-si- - Google Patents

Composés catalyseurs métallocènes de type bis-indényle substitué comprenant un pont -si-si- Download PDF

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WO2017011073A1
WO2017011073A1 PCT/US2016/033583 US2016033583W WO2017011073A1 WO 2017011073 A1 WO2017011073 A1 WO 2017011073A1 US 2016033583 W US2016033583 W US 2016033583W WO 2017011073 A1 WO2017011073 A1 WO 2017011073A1
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catalyst
group
ring
borate
polymer
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PCT/US2016/033583
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English (en)
Inventor
Jian Yang
Matthew W. Holtcamp
Gregory S. DAY
Xiongdong Lian
Xuan YE
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Exxonmobil Chemical Patents Inc.
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Priority to EP16824842.5A priority Critical patent/EP3322529A4/fr
Priority to BR112018000843A priority patent/BR112018000843A2/pt
Priority to CN201680041437.7A priority patent/CN107847920A/zh
Publication of WO2017011073A1 publication Critical patent/WO2017011073A1/fr

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    • 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
    • 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
    • C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
    • C08F2410/07—Catalyst support treated by an anion, e.g. Cl-, F-, SO42-
    • 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
    • C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
    • C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
    • 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
    • C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
    • C08F4/65916—Component covered by group C08F4/64 containing a transition metal-carbon bond supported on a carrier, e.g. silica, MgCl2, polymer

Definitions

  • This invention relates to novel catalyst compounds comprising -Si-Si- bridges, catalyst systems comprising such, and uses thereof.
  • Olefin polymerization catalysts are of great use in industry. Hence there is interest in finding new catalyst systems that increase the commercial usefulness of the catalyst and allow the production of polymers having improved properties.
  • Catalysts for olefin polymerization are often based on transition metal compounds, e.g., metallocenes, as catalyst precursors, which are activated either with the help of alumoxane, or with an activator containing a non-coordinating anion.
  • transition metal compounds e.g., metallocenes
  • WO 2002/002576 discloses metallocene compositions and their use in the preparation of catalyst systems for olefin polymerization, particularly propylene polymerization.
  • the bridged bis (2-R -4-phenyl-indenyl) metallocenes described therein include those wherein at least one of the phenyl rings is substituted at the 3' and 5' positions by butyl groups which may be the same or different, e.g., tert-butyl.
  • This invention relates to a novel bridged transition metal complexes represented by the formula (I):
  • M 1 is selected from the group consisting of titanium, zirconium, hafnium; each R 1 and R 2 are identical or different and are each a hydrogen atom, a Ci-Cio alkyl group, a Ci-Cio alkoxy group, a C6-C10 aryl group, a C6-C10 aryloxy group, a C2-C10 alkenyl group, a C2-C40 alkenyl group, a C7-C40 arylalkyl group, a C7-C40 alkylaryl group, a C8-C40 (preferably C8-C30) arylalkenyl group, an OH group or a halogen atom, or a conjugated diene which is, optionally, substituted with one or more hydrocarbyl, tri (hydrocarbyl) silyl groups or tri (hydrocarbyl) silylhydrocarbyl groups, said diene having up to 30 atoms not counting hydrogen;
  • each R 3 to R 7 are identical or different and are each a hydrogen atom, or a substituted or unsubstituted, branched or unbranched Ci-Cio alkyl group which may be halogenated;
  • R 13 is -((R 15 *) 2 Si-Si(R 15 ) 2 )- wherein, each R 15 and R 15 * is identical or different and is a substituted or unsubstituted, branched or unbranched C1-C2 0 alkyl group;
  • each R 8 , R 10 , and R 12 are identical or different and are each a hydrogen atom or a substituted or unsubstituted, branched or unbranched, C1-C1 0 alkyl group which may be halogenated;
  • each R 9 and R 11 are identical or different and are a hydrogen atom or a substituted or unsubstituted, branched or unbranched, C2-C2 0 alkyl group which may be halogenated.
  • embodiments of the invention provide an -Si-Si- bridged bis(4- phenyl-indenyl) transition metal complex wherein R 3 is a hydrogen atom and R 9 and R 11 are each t-butyl groups.
  • each R 15 together do not form a ring, and/or each
  • R 15 * together do not form a ring, and/or R 15 and R 15 * together do not form a ring.
  • embodiments of the invention provide a transition metal complex represented by the formula (I) above, wherein M 1 is Zr, Hf or Ti, R 3 is a hydrogen atom or a C1-C1 0 alkyl group, R 8 , R 10 , and R 12 are each hydrogen atoms and R 9 and R 11 are identical or different and are each a C3-C2 0 alkyl group.
  • embodiments of the invention provide a catalyst system comprising an activator and a transition metal complex as described herein.
  • embodiments of the invention provide a polymerization process comprising: a) contacting one or more alkene monomers (such as ethylene) with a catalyst system comprising: i) an activator and ii) a transition metal complex described herein.
  • embodiments of the invention provide a polymerization process to produce a polymer blend (preferably a bimodal polymer composition) comprising: a) contacting one or more alkene monomers (such as ethylene) with a catalyst system comprising: i) an activator, ii) a transition metal complex described above, and (iii) a second catalyst compound.
  • a polymer blend preferably a bimodal polymer composition
  • a catalyst system comprising: i) an activator, ii) a transition metal complex described above, and (iii) a second catalyst compound.
  • This invention further relates to polymer compositions produced by the methods described herein.
  • the catalysts and catalyst systems described herein provide polymers, such as polyethylene polymers wherein incorporation of comonomers, such as C3 to Cg alkylene monomers, is less than 20%, more preferably less than 15% and even more preferably less than 10% by weight of the copolymer and with high molecular weights while maintaining good catalyst activities.
  • comonomers such as C3 to Cg alkylene monomers
  • the embodiments described herein pertain to novel catalyst compounds, catalysts systems comprising such compounds, and processes for the polymerization of olefins using such compounds and systems.
  • FIG. 1 is a representative plot of 1-hexene Incorporation (C6 wt%) vs 1-hexene Loading for Catalyst 1 in comparison to Catalysts 2-4 in Table 1.
  • FIG. 2 is a representative plot of Mw vs 1-hexene Incorporation (C6 wt%) for Catalyst 1 in comparison to Catalyst 2 in Table 1.
  • FIG. 3 is a representative plot of Mw (k) vs 1-hexene in feed for Poor Comonomer Incorporating Catalysts in Table 2.
  • FIG. 4 is a Plot of Mw (k) vs C6 wt% for Catalyst 8 in comparison to Catalyst 5 in
  • FIG. 5 is a comparison of activities of Catalysts 10, 11, and 12 from Table 3.
  • FIG. 6 is a comparison of molecular weights of polymers made by Catalysts 10, 11, and 12 from Table 3.
  • FIG. 7 is a representative plot of melt index (MI) vs. 1-hexene loadings for Catalyst 10,
  • FIGs. 8A and 8B are plots of dynamic rheological measurements of polymers made by
  • FIGs. 8C and 8D are plots of dynamic rheological measurements of polymers made by Catalysts 10, 11, and 12 (Runs 2, 4, and 6 from Table 3).
  • FIGs. 9A, 9B, 9C, and 9D are the GPC of polyethylene made by Catalyst 10 (Table 3, Run 1).
  • FIGs. 10A, 10B, IOC, and 10D are the GPC of ethylene 1-hexene copolymers made by Catalyst 10 (Table 3, Run 2).
  • a "group 4 metal” is an element from group 4 of the Periodic Table, e.g., Hf, Ti, or Zr.
  • transition metal complexes The term complex is used to describe molecules in which an ancillary ligand is coordinated to a central transition metal atom.
  • the ligand is bulky and stably bonded to the transition metal so as to maintain its influence during use of the catalyst, such as polymerization.
  • the ligand may be coordinated to the transition metal by covalent bond and/or electron donation coordination or intermediate bonds.
  • the transition metal complexes are generally subjected to activation to perform their polymerization or oligomerization function using an activator which is believed to create a cation as a result of the removal of an anionic group, often referred to as a leaving group, from the transition metal.
  • Catalyst productivity is a measure of how many grams of polymer (P) are produced using a polymerization catalyst comprising W g of catalyst (cat), over a period of time of T hours; and may be expressed by the following formula: P/(T x W) and expressed in units of gPgcaHhr 1 . Conversion is the amount of monomer that is converted to polymer product, and is reported as mol% and is calculated based on the polymer yield and the amount of monomer fed into the reactor. Catalyst activity is a measure of how active the catalyst is and is reported as the mass of product polymer (P) produced per mole of catalyst (cat) used (kgP/molcat).
  • an “olefin,” alternatively referred to as “alkene,” is a linear, branched, or cyclic compound of carbon and hydrogen having at least one double bond.
  • alkene is a linear, branched, or cyclic compound of carbon and hydrogen having at least one double bond.
  • a copolymer when a copolymer is said to have an "ethylene" content of 35 wt% to 55 wt%, it is understood that the mer unit in the copolymer is derived from ethylene in the polymerization reaction and said derived units are present at 35 wt% to 55 wt%, based upon the weight of the copolymer.
  • a "polymer” has two or more of the same or different mer units.
  • a “homopolymer” is a polymer having mer units that are the same.
  • a “copolymer” is a polymer having two or more mer units that are different from each other.
  • a “terpolymer” is a polymer having three mer units that are different from each other.
  • ethylene polymer or "ethylene copolymer” is a polymer or copolymer comprising at least 50 mol% ethylene derived units
  • ethylene copolymer is a polymer or copolymer comprising at least 50 mol% propylene derived units
  • ethylene polymer or "ethylene copolymer” is a polymer or copolymer comprising at least 50 mol% ethylene derived units
  • a "propylene polymer” or “propylene copolymer” is a polymer or copolymer comprising at least 50 mol% propylene derived units, and so on.
  • ethylene shall be considered an a-olefin.
  • substituted means that a hydrogen group has been replaced with a heteroatom, or a heteroatom-containing group.
  • a “substituted hydrocarbyl” is a radical made of carbon and hydrogen where at least one hydrogen is replaced by a heteroatom or heteroatom-containing group.
  • Mn is number average molecular weight
  • Mw is weight average molecular weight
  • Mz is z average molecular weight
  • wt% is weight percent
  • mol% is mole percent.
  • Molecular weight distribution also referred to as polydispersity (PDI)
  • PDI polydispersity
  • dme is 1 ,2-dimethoxy ethane
  • Me is methyl
  • Ph is phenyl
  • Et is ethyl
  • Pr is propyl
  • iPr is isopropyl
  • n-Pr is normal propyl
  • Bu is butyl
  • cPR is cyclopropyl
  • iBu is isobutyl
  • tBu is tertiary butyl
  • p-tBu is para-tertiary butyl
  • nBu is normal butyl
  • sBu is sec-butyl
  • TMS is trimethylsilyl
  • TIBAL is triisobutylaluminum
  • TNOAL is tri(n-octyl)aluminum
  • MAO is methylalumoxane
  • p-Me is para-methyl
  • Ph is phenyl
  • Bn is benzyl (i.e., CH 2 Ph)
  • THF also
  • a “catalyst system” comprises at least one catalyst compound and at least one activator.
  • Catalyst system when “catalyst system” is used to describe such the catalyst compound/activator combination before activation, it means the unactivated catalyst complex (precatalyst) together with an activator and, optionally, a co-activator.
  • combination after activation when it is used to describe the combination after activation, it means the activated complex and the activator or other charge-balancing moiety.
  • the transition metal compound may be neutral as in a precatalyst, or a charged species with a counter ion as in an activated catalyst system.
  • catalyst systems are described as comprising neutral stable forms of the components, it is well understood by one of ordinary skill in the art, that the ionic form of the component is the form that reacts with the monomers to produce polymers.
  • the metallocene catalyst may be described as a catalyst precursor, a pre-catalyst compound, metallocene catalyst compound or a transition metal compound, and these terms are used interchangeably.
  • a polymerization catalyst system is a catalyst system that can polymerize monomers to polymer.
  • An "anionic ligand” is a negatively charged ligand which donates one or more pairs of electrons to a metal ion.
  • a "neutral donor ligand” is a neutrally charged ligand which donates one or more pairs of electrons to a metal ion.
  • Activator and cocatalyst are also used interchangeably.
  • a scavenger is a compound that is typically added to facilitate polymerization by scavenging impurities. Some scavengers may also act as activators and may be referred to as co-activators. A co-activator, that is not a scavenger, may also be used in conjunction with an activator in order to form an active catalyst. In some embodiments a co-activator can be pre-mixed with the transition metal compound to form an alkylated transition metal compound.
  • Non-coordinating anion is defined to mean an anion either that does not coordinate to the catalyst metal cation or that does coordinate to the metal cation, but only weakly.
  • NCA is also defined to include multicomponent NCA-containing activators, such as N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate, that contain an acidic cationic group and the non-coordinating anion.
  • NCA is also defined to include neutral Lewis acids, such as tris(pentafluorophenyl)boron, that can react with a catalyst to form an activated species by abstraction of an anionic group.
  • NCA coordinates weakly enough that a neutral Lewis base, such as an olefinically or acetylenically unsaturated monomer can displace it from the catalyst center.
  • a neutral Lewis base such as an olefinically or acetylenically unsaturated monomer can displace it from the catalyst center.
  • Any metal or metalloid that can form a compatible, weakly coordinating complex may be used or contained in the non- coordinating anion.
  • Suitable metals include, but are not limited to, aluminum, gold, and platinum.
  • Suitable metalloids include, but are not limited to, boron, aluminum, phosphorus, and silicon.
  • Activators containing non-coordinating anions can also be referred to as stoichiometric activators.
  • a stoichiometric activator can be either neutral or ionic.
  • ionic activator and stoichiometric ionic activator can be used interchangeably.
  • neutral stoichiometric activator and Lewis acid activator can be used interchangeably.
  • non-coordinating anion activator includes neutral stoichiometric activators, ionic stoichiometric activators, ionic activators, and Lewis acid activators.
  • a metallocene catalyst is defined as an organometallic compound with at least one ⁇ - bound cyclopentadienyl moiety (or substituted cyclopentadienyl moiety) and more frequently two ⁇ -bound cyclopentadienyl moieties or substituted cyclopentadienyl moieties.
  • substituted means that a hydrogen group has been replaced with a hydrocarbyl group, a heteroatom, or a heteroatom-containing group.
  • methyl cyclopentadiene (Cp) is a Cp group substituted with a methyl group.
  • alkoxides include those where the alkyl group is a to C 10 hydrocarbyl.
  • the alkyl group may be straight chain, branched, or cyclic.
  • the alkyl group may be saturated or unsaturated.
  • the alkyl group may comprise at least one aromatic group.
  • hydrocarbyl radical is defined to be CI -CI 00 radicals, that may be linear, branched, or cyclic, and when cyclic, aromatic or non-aromatic.
  • radicals include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, octyl cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctyl, and the like including their substituted analogues.
  • Substituted hydrocarbyl radicals are radicals in which at least one hydrogen atom of the hydrocarbyl radical has been substituted with at least one halogen (such as Br, CI, F or I) or at least one functional group such as NR*2, OR*, SeR*, TeR*, PR*2, AsR*2, SbR*2, SR*, BR*2, SiR*3, GeR*3, SnR*3, PbR*3, and the like, or where at least one heteroatom has been inserted within a hydrocarbyl ring.
  • at least one hydrogen atom of the hydrocarbyl radical has been substituted with at least one halogen (such as Br, CI, F or I) or at least one functional group such as NR*2, OR*, SeR*, TeR*, PR*2, AsR*2, SbR*2, SR*, BR*2, SiR*3, GeR*3, SnR*3, PbR*3, and the like, or where at least one heteroatom has been inserted within
  • alkenyl means a straight-chain, branched-chain, or cyclic hydrocarbon radical having one or more double bonds. These alkenyl radicals may be optionally substituted. Examples of suitable alkenyl radicals include, but are not limited to, ethenyl, propenyl, allyl, 1 ,4-butadienyl cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloctenyl, and the like, including their substituted analogues.
  • alkoxy or "alkoxide” means an alkyl ether or aryl ether radical wherein the term alkyl is as defined above.
  • suitable alkyl ether radicals include, but are not limited to, methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, sec-butoxy, tert- butoxy, phenoxyl, and the like.
  • aryl or “aryl group” means a six carbon aromatic ring and the substituted variants thereof, including but not limited to, phenyl, 2-methyl-phenyl, xylyl, 4-bromo-xylyl.
  • heteroaryl means an aryl group where a ring carbon atom (or two or three ring carbon atoms) has been replaced with a heteroatom, preferably N, O, or S.
  • aromatic also refers to pseudoaromatic heterocycles which are heterocyclic substituents that have similar properties and structures (nearly planar) to aromatic heterocyclic ligands, but are not by definition aromatic; likewise the term aromatic also refers to substituted aromatics.
  • isomers of a named alkyl, alkenyl, alkoxide, or aryl group exist (e.g., n-butyl, iso-butyl, sec-butyl, and tert-butyl) reference to one member of the group (e.g., n-butyl) shall expressly disclose the remaining isomers (e.g., iso-butyl, sec-butyl, and tert-butyl) in the family.
  • alkyl, alkenyl, alkoxide, or aryl group without specifying a particular isomer (e.g., butyl) expressly discloses all isomers (e.g., n-butyl, iso-butyl, sec- butyl, and tert-butyl).
  • ring atom means an atom that is part of a cyclic ring structure.
  • a benzyl group has six ring atoms and tetrahydrofuran has 5 ring atoms.
  • a heterocyclic ring is a ring having a heteroatom in the ring structure as opposed to a heteroatom-substituted ring where a hydrogen on a ring atom is replaced with a heteroatom.
  • tetrahydrofuran is a heterocyclic ring and 4-N,N-dimethylamino-phenyl is a heteroatom-substituted ring.
  • continuous means a system that operates without interruption or cessation.
  • a continuous process to produce a polymer would be one where the reactants are continually introduced into one or more reactors and polymer product is continually withdrawn.
  • a solution polymerization means a polymerization process in which the polymer is dissolved in a liquid polymerization medium, such as an inert solvent or monomer(s) or their blends.
  • a solution polymerization is typically homogeneous.
  • a homogeneous polymerization is one where the polymer product is dissolved in the polymerization medium.
  • Such systems are preferably not turbid as described in J. Vladimir Oliveira, C. Dariva and J. C. Pinto, Ind. Eng. Chem. Res., 2000, Vol. 29, p. 4627.
  • a bulk polymerization means a polymerization process in which the monomers and/or comonomers being polymerized are used as a solvent or diluent using little or no inert solvent as a solvent or diluent.
  • a small fraction of inert solvent might be used as a carrier for catalyst and scavenger.
  • a bulk polymerization system contains less than 25 wt% of inert solvent or diluent, preferably less than 10 wt%, preferably less than 1 wt%, preferably 0 wt%.
  • the invention relates to novel bridged metallocene transition metal complexes, where the complexes include at least one indenyl ligand substituted at the 4-position with a phenyl group, the phenyl group being substituted at the 3' and 5' (R 9 and R 11 ) positions with particular combinations of substituents and bridged with an -Si-Si- group.
  • the R 9 and R 10 positions of the phenyl ring are selected to be sterically hindering (e.g., branched hydrocarbyl groups).
  • this invention relates to a catalyst compound, and catalyst systems comprising such compounds, represented by the formula (I):
  • M 1 is selected from the group consisting of titanium, zirconium, hafnium (preferably zirconium and hafnium, preferably zirconium);
  • each R 1 and R 2 are identical or different, and are each a hydrogen atom or a substituted or unsubstituted, branched or unbranched C1-C2 0 alkyl group;
  • each R 3 to R 7 are identical or different and are each a hydrogen atom, or a substituted or unsubstituted, branched or unbranched C1-C1 0 alkyl group which may be halogenated;
  • R 13 is -((R 15 *) 2 Si-Si(R 15 ) 2 )- wherein, each R 15 and R 15 * is identical or different and is a substituted or unsubstituted, branched or unbranched C1-C2 0 alkyl group (preferably each R 15 together do not form a ring, and/or each R 15 * together do not form a ring, and/or R 15 and R 15 * together do not form a ring);
  • each R 8 , R 10 and R 12 are identical or different and are each a hydrogen atom or a substituted or unsubstituted, branched or unbranched C1-C1 0 alkyl group which may be halogenated;
  • each R 9 and R 11 are identical or different and are a hydrogen atom or a substituted or unsubstituted, branched or unbranched C2-C2 0 alkyl group which may be halogenated.
  • M 1 is Hf, Zr or Ti, preferably Hf or Zr, preferably Zr.
  • each R 15 is preferably a methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, or dodecyl group.
  • each R 15 * is preferably a methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, or dodecyl group.
  • R 13 is represented by the formula -((R 15 *)2Si-Si(R 15 )2)-, and each R 15 and R 15 * is, independently, a to C 2 o hydrocarbyl (such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, or dodecyl) or a to C 20 substituted hydrocarbyl.
  • R 13 is the bridging group -(Me 2 )Si-Si(Me 2 )-.
  • each R 15 together do not form a ring and each R 15 * together do not form a ring.
  • each R 15 together do not form a ring.
  • R 15 and R 15 * together do not form a ring.
  • each R together do not form a ring, and each R together do not form a ring, and R 15 and R 15 * together do not form a ring.
  • each R 1 and R 2 is, independently, selected from the group consisting of hydrocarbyl radicals having from 1 to 20 carbon atoms, hydrides, amides, alkoxides, sulfides, phosphides, halides, dienes, amines, phosphines, ethers, and a combination thereof, (R 1 and R 2 may form a part of a fused ring or a ring system), preferably each R 1 and R 2 is independently selected from halides and to C 5 alkyl groups (preferably methyl groups).
  • R 1 and R 2 are selected from chloro, bromo, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, and dodecyl.
  • R 1 and R 2 may also be joined together to form an alkanediyl group or a conjugated C4-C40 diene ligand which is coordinated to M in a metallocyclopentene fashion;
  • R 1 and R 2 may also be identical or different conjugated dienes, optionally substituted with one or more hydrocarbyl, tri (hydrocarbyl) silyl groups or tri (hydrocarbyl) silylhydrocarbyl groups, said dienes having up to 30 atoms not counting hydrogen and forming a ⁇ -complex with M 1 .
  • R 1 and or R 2 include 1,4-diphenyl, 1,3-butadiene, 1,3- pentadiene, 2-methyl 1,3-pentadiene, 2,4-hexadiene, 1-phenyl, 1,3-pentadiene, 1,4-dibenzyl, 1,3-butadiene, l,4-ditolyl-l,3-butadiene, 1,4-bis (trimethylsilyl)- 1,3 -butadiene, and 1,4- dinaphthyl-l,3-butadiene; preferably R 1 and R 2 are identical and are a C1-C3 alkyl or alkoxy group, a C6-C10 aryl or aryloxy group, a C2-C4 alkenyl group, a C7-C10 arylalkyl group, a C 7 - C12 alkylaryl group, or a halogen atom, particularly chlorine.
  • the 2 position of the indenyl group or groups, e.g., R 3 in formula I may be selected from hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, octyl cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctyl, or a substituted or unsubstituted phenyl, particularly methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, more particularly hydrogen or methyl.
  • the 2 position of the indenyl group or groups, e.g., R 3 in formula I, is hydrogen.
  • R 4 , R 5 , R 6 , and R 7 of formula I may be identical or different and are each a hydrogen atom, a halogen atom, a C1-C10 alkyl group (methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof) which may be halogenated, or a C6-C1 0 aryl group which may be halogenated.
  • a C1-C10 alkyl group methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof
  • a C6-C1 0 aryl group which may be halogenated.
  • R 8 , R 10 , and R 12 of formula I may be identical or different and are each a hydrogen atom, a halogen atom, a C1-C1 0 alkyl group (preferably C2 to Cio, preferably C3 to C1 0 , preferably methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof) which may be halogenated, a Ce- C1 0 aryl group which may be halogenated, preferably methyl, ethyl, propyl, butyl, pentyl, hexyl, phenyl, octyl, nonyl, decyl, undecyl, dodecyl, preferably methyl, ethyl, or phenyl.
  • R 9 and R 11 of formula I are identical or different and selected from a hydrogen atom, C2-C2 0 alkyl group (preferably C3 to Ci 6 , preferably C4 to C12, preferably butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and isomers thereof) which may be halogenated, a C6-C1 0 aryl group which may be halogenated.
  • C2-C2 0 alkyl group preferably C3 to Ci 6 , preferably C4 to C12, preferably butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and isomers thereof
  • C6-C1 0 aryl group which may be halogenated.
  • R 9 and R 11 may be the same or different and are each a butyl group, an aryl group, an isopropyl group, or a fluoroalkyl group, particularly wherein each of R 9 and R 11 is selected from the group consisting of propyl, isopropyl, n-propyl, n-butyl-, iso-butyl-, and tert-butyl groups.
  • R 9 and R 11 may be the same or different and are each a butyl group, an aryl group, an isopropyl group, or a fluoroalkyl group, particularly wherein each of R 9 and R 11 is selected from the group consisting of propyl, isopropyl, n-propyl, n- butyl-, iso-butyl-, and tert-butyl groups and R 10 may be -NR' 2 , -SR', -OR', -OSiR' 3 , or a -PR'2 radical, wherein R' is one of a hydrogen atom, halogen atom, a C1-C1 0 alkyl group, or a C6-C1 0 aryl group, particularly wherein R 10 is OR' wherein R' is a C1-C1 0 alkyl group, particularly a methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy
  • R 3 is a hydrogen atom and each of R 9 and R 11 is one of n-butyl-, iso-butyl-, and particularly tert-butyl groups.
  • R 3 is a hydrogen atom
  • each of R 9 and R 11 is a hydrogen atom
  • R 8 , R 10 , and R 12 are each hydrogen atoms.
  • R 3 is a hydrogen atom or a substituted or unsubstituted, branched or unbranched C1-C1 0 alkyl group and each of R 9 and R 11 is a substituted or unsubstituted, branched or unbranched C1-C2 0 alkyl group, preferably a C2-C2 0 alkyl group.
  • R 13 is the bridging group -(Me2)Si-Si(Me2)-.
  • transition metal complexes are Zr-based or Hf-based complexes. Additionally, some such transition metal complexes are bridged by a dialkyldisiladiyl group.
  • Particularly preferred transition metal complexes of the present invention are represented the formula (I) above, wherein M 1 is selected from the group consisting of titanium, zirconium, and hafnium, particularly zirconium or hafnium, more typically zirconium; R 1 and R 2 are identical or different, and are one of a hydrogen atom, a Ci-Cio alkyl group (preferably methyl, ethyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and isomers thereof), or a halogen atom (preferably CI, Br, F or I).
  • the R 3 groups may be identical or different and are each a hydrogen atom, a Ci-Cio alkyl group (preferably C 2 to Cio, preferably C3 to Cg, preferably methyl, ethyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof) which may be halogenated, a C6-C 10 aryl group which may be halogenated.
  • each R 3 may be the same or different and are each a C 1 -C 10 alkyl group.
  • R 3 is not a hydrogen atom, e.g., in particular embodiments, each R 3 is identical and is a C 1 -C4 alkyl group which may be halogenated.
  • the R 4 to R 7 groups are identical or different and may be hydrogen or a C 1 -C 10 alkyl group (preferably methyl, ethyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl or an isomer thereof) which may be halogenated.
  • two or more adjacent radicals R 5 to R 7 together with the atoms connecting them form one or more rings, preferably a 6-membered ring, preferably 4, 5, 6, 7 or 8 membered ring.
  • R 13 is -(R") 2 Si-Si(R") 2 - wherein the R" groups may be the same or different and are each selected from a hydrogen or a C1-C10 alkyl group, preferably a C 1 -C 2 alkyl group (e.g., methyl or ethyl).
  • each R 9 and R 11 may be identical or different and are each a C2-C20 alkyl group which may be halogenated.
  • each R 9 and each R 11 is selected from the group consisting of primary, secondary or tertiary butyl groups, isopropyl groups, fluoroalkyl groups, preferably a tertiary butyl group, particularly n-butyl-, iso-butyl-, and tert-butyl groups.
  • each R 1 and R 2 may be the same or different and are each a halogen atom, preferably CI; each R 3 may be the same or different and are each a hydrogen atom or a C1-C10 alkyl group, preferably methyl; each R 4 , R 5 , R 6 , and R 7 may be the same or different and are each a hydrogen atom or C 1 -C 10 alkyl group, preferably each is a hydrogen atom; each R 8 and R 12 are each a hydrogen atom; R 13 is -(R")2Si-Si(R")2- wherein each R" may be the same or different and are each a hydrogen or Ci-Cio alkyl group, preferably methyl; each R 9 and R 11 is a C2-C1 0 alkyl group, particularly a tert-butyl group; and wherein each R 10 is hydrogen or a C1-C1 0 alkyl group.
  • transition metal complexes according to formula (I) include those wherein R and R are chlorine; each R is a hydrogen atom; each R , R , R , and R , R 8 , R 10 and R 12 are hydrogen; R 13 is -(CH 3 ) 2 Si-Si(CH 3 ) 2 -, and each R 9 and R 11 is a tert-butyl group.
  • M 1 is zirconium.
  • transition metal complexes according to formula (I) include those wherein each M is zirconium, R 1 and R 2 are chlorine; each R 3 is a hydrogen atom; each R 4 , R 5 , R 6 , and R 7 , R 8 , R 10 , and R 12 are hydrogen; R 13 is -(CH 3 ) 2 Si-Si(CH 3 ) 2 -, and each R 9 and R 11 is a hydrogen atom.
  • M 1 is zirconium.
  • transition metal complexes according to formula (I) include those wherein R 1 and R 2 are chlorine; each R 3 is a C1-C1 0 alkyl group; each R 4 , R 5 , R 6 , and each R 7 , R 8 , R 10 , and R 12 are hydrogen; R 13 is -(CH 3 ) 2 Si-Si(CH 3 ) 2 -, and each R 9 and R 11 is a tert-butyl group.
  • M 1 is zirconium.
  • zirconium-containing metallocenes and their hafnium- containing analogs are expressly disclosed: rac-tetramethyldisilylene bis(4-(3',5 '-di-tert- butylphenyl)-indenyl) zirconium dichloride, meso-tetramethyldisilylene bis(4-(3',5 '-di-tert- butylphenyl)-indenyl) zirconium dichloride.
  • the rac/meso ratio of the metallocene catalyst is 50: 1 or greater, or 40: 1 or greater, or 30: 1 or greater, or 20: 1 or greater, or 15: 1 or greater, or 10: 1 or greater, or 7: 1 or greater, or 5 : 1 or greater.
  • the metallocene catalyst comprises greater than 55 mol% of the racemic isomer, or greater than 60 mol% of the racemic isomer, or greater than 65 mol% of the racemic isomer, or greater than 70 mol% of the racemic isomer, or greater than 75 mol% of the racemic isomer, or greater than 80 mol% of the racemic isomer, or greater than 85 mol% of the racemic isomer, or greater than 90 mol% of the racemic isomer, or greater than 92 mol% of the racemic isomer, or greater than 95 mol% of the racemic isomer, or greater than 98 mol% of the racemic isomer, based on the total amount of the racemic and meso isomer-if any, formed.
  • the bridged bis(indenyl)metallocene transition metal compound formed consists essentially of the racemic isomer.
  • an advantage is provided in that the need for the separation of meso from rac isomers is not required for the catalysts disclosed herein.
  • the meso isomer is more active than the rac isomer.
  • Amounts of rac and meso isomers are determined by proton NMR.
  • l H NMR data are collected at 23°C in a 5 mm probe using a 400 MHz Bruker spectrometer with deuterated benzene or deuterated chloroform. Data is recorded using a maximum pulse width of 45°, 8 sec. between pulses and signal averaging 16 transients.
  • the spectrum is normalized to protonated benzene in the deuterated benzene, which is expected to show a peak at 7.16 ppm.
  • one catalyst compound is used, e.g., the catalyst compounds are not different.
  • one metallocene catalyst compound is considered different from another if they differ by at least one atom.
  • "bisindenyl zirconium dichloride” is different from "(indenyl)(2-methylindenyl) zirconium dichloride” which is different from "(indenyl)(2- methylindenyl) hafnium dichloride.”
  • Catalyst compounds that differ only by isomer are considered the same for purposes if this invention, e.g., rac-dimethylsilylbis(2-methyl 4- phenyl)hafhium dimethyl is considered to be the same as meso-dimethylsilylbis(2 -methyl 4- phenyl)hafhium dimethyl.
  • two or more different catalyst compounds are present in the catalyst system used herein. In some embodiments, two or more different catalyst compounds are present in the reaction zone where the process(es) described herein occur.
  • the two transition metal compounds are preferably chosen such that the two are compatible.
  • a simple screening method such as by X H or 1 C NMR, known to those of ordinary skill in the art, can be used to determine which transition metal compounds are compatible. It is preferable to use the same activator for the transition metal compounds, however, two different activators, such as a non-coordinating anion activator and an alumoxane, can be used in combination.
  • transition metal compounds contain an Xi or X 2 ligand which is not a hydride, hydrocarbyl, or substituted hydrocarbyl, then the alumoxane should be contacted with the transition metal compounds prior to addition of the non- coordinating anion activator.
  • the two transition metal compounds may be used in any ratio.
  • Preferred molar ratios of (A) transition metal compound to (B) transition metal compound fall within the range of (A:B) 1 :1000 to 1000:1, alternatively 1 :100 to 500:1, alternatively 1 :10 to 200:1, alternatively 1 :1 to 100:1, and alternatively 1 :1 to 75:1, and alternatively 5: 1 to 50:1.
  • the particular ratio chosen will depend on the exact pre-catalysts chosen, the method of activation, and the end product desired.
  • useful mole percents are 10 to 99.9% A to 0.1 to 90% B, alternatively
  • metallocenes of this type are synthesized as shown below where (i) is a deprotonation via a metal salt of alkyl anion (e.g., "BuLi) to form an indenide; (ii) reaction of indenide with an appropriate bridging precursor (e.g., ClMe2SiSiMe2Cl); (iii) double deprotonation via an alkyl anion (e.g., "BuLi) to form a dianion; (iv) reaction of the dianion with a metal halide (e.g., ZrCl 4 ); and (v).
  • the final products are obtained by crystallization separation of the crude solids.
  • catalyst and “activator” are used herein interchangeably and are defined to be any compound which can activate any one of the catalyst compounds described above by converting the neutral catalyst compound to a catalytically active catalyst compound cation.
  • catalyst systems may be formed by combining them with activators in any manner known from the literature including by supporting them for use in slurry or gas phase polymerization.
  • the catalyst systems may also be added to or generated in solution polymerization or bulk polymerization (in the monomer).
  • the catalyst system typically comprise a complex as described above and an activator such as alumoxane or a non-coordinating anion.
  • Non-limiting activators include alumoxanes, aluminum alkyls, ionizing activators, which may be neutral or ionic, and conventional-type cocatalysts.
  • Preferred activators typically include alumoxane compounds, modified alumoxane compounds, and ionizing anion precursor compounds that abstract a reactive, ⁇ -bound, metal ligand making the metal complex cationic and providing a charge-balancing non-coordinating or weakly coordinating anion.
  • alumoxane activators are utilized as an activator in the catalyst system.
  • Alumoxanes are generally oligomeric compounds containing -Al(R!)-0- sub-units, where R 1 is an alkyl group.
  • Examples of alumoxanes include methylalumoxane (MAO), modified methylalumoxane (MMAO), ethylalumoxane and isobutylalumoxane.
  • Alkylalumoxanes and modified alkylalumoxanes are suitable as catalyst activators, particularly when the abstractable ligand is an alkyl, halide, alkoxide or amide.
  • alumoxanes Mixtures of different alumoxanes and modified alumoxanes may also be used. It may be preferable to use a visually clear methylalumoxane.
  • a cloudy or gelled alumoxane can be filtered to produce a clear solution or clear alumoxane can be decanted from the cloudy solution.
  • a useful alumoxane is a modified methyl alumoxane (MMAO) cocatalyst type 3A (commercially available from Akzo Chemicals, Inc. under the trade name Modified Methylalumoxane type 3 A, covered under US 5,041 ,584).
  • MMAO modified methyl alumoxane
  • some embodiments select the maximum amount of activator typically at up to a 5000-fold molar excess Al/M over the catalyst compound (per metal catalytic site).
  • the minimum activator-to-catalyst-compound is a 1 : 1 molar ratio.
  • Altemate preferred ranges include from 1 : 1 to 500: 1, alternately from 1 : 1 to 200: 1 , alternately from 1 : 1 to 100: 1, or alternately from 1 : 1 to 50: 1.
  • alumoxane is present at zero mole %, alternately the alumoxane is present at a molar ratio of aluminum to catalyst compound transition metal less than 500: 1 , preferably less than 300: 1, preferably less than 100: 1, preferably less than 1 : 1.
  • Non-Coordinating Anion Activators are used in the polymerization processes described herein.
  • NCA non-coordinating anion
  • NCA is defined to mean an anion either that does not coordinate to the catalyst metal cation or that does coordinate to the metal cation, but only weakly.
  • NCA is also defined to include multicomponent NCA-containing activators, such as N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate, that contain an acidic cationic group and the non-coordinating anion.
  • NCA is also defined to include neutral Lewis acids, such as tris(pentafluorophenyl)boron, that can react with a catalyst to form an activated species by abstraction of an anionic group.
  • NCA coordinates weakly enough that a neutral Lewis base, such as an olefinically or acetylenically unsaturated monomer can displace it from the catalyst center.
  • a neutral Lewis base such as an olefinically or acetylenically unsaturated monomer can displace it from the catalyst center.
  • Any metal or metalloid that can form a compatible, weakly coordinating complex may be used or contained in the non- coordinating anion. Suitable metals include, but are not limited to, aluminum, gold, and platinum. Suitable metalloids include, but are not limited to, boron, aluminum, phosphorus, and silicon.
  • a stoichiometric activator can be either neutral or ionic. The terms ionic activator, and stoichiometric ionic activator can be used interchangeably.
  • neutral stoichiometric activator and Lewis acid activator can be used interchangeably.
  • non-coordinating anion includes neutral stoichiometric activators, ionic stoichiometric activators, ionic activators, and Lewis acid activators.
  • Non-coordinating anions are those which are not degraded to neutrality when the initially formed complex decomposes. Further, the anion will not transfer an anionic substituent or fragment to the cation so as to cause it to form a neutral transition metal compound and a neutral by-product from the anion.
  • Non-coordinating anions useful in accordance with this invention are those that are compatible, stabilize the transition metal cation in the sense of balancing its ionic charge at +1 , and yet retain sufficient lability to permit displacement during polymerization.
  • an ionizing or stoichiometric activator such as tri (n-butyl) ammonium tetrakis (pentafluorophenyl) borate, a tris perfluorophenyl boron metalloid precursor or a tris perfluoronaphthyl boron metalloid precursor, polyhalogenated heteroborane anions (WO 98/43983), boric acid (US 5,942,459), or combination thereof. It is also within the scope of this invention to use neutral or ionic activators alone or in combination with alumoxane or modified alumoxane activators.
  • the catalyst systems of this invention can include at least one non-coordinating anion (NCA) activator.
  • NCA non-coordinating anion
  • Z is (L-H) or a reducible Lewis acid
  • L is a neutral Lewis base
  • H is hydrogen
  • (L-H) is a Bronsted acid;
  • a d" is a boron containing non-coordinating anion having the charge d-;
  • d is 1, 2, or 3.
  • the cation component, Z d + may include Bronsted acids such as protons or protonated Lewis bases or reducible Lewis acids capable of protonating or abstracting a moiety, such as an alkyl or aryl, from the bulky ligand metallocene containing transition metal catalyst precursor, resulting in a cationic transition metal species.
  • the activating cation Z d + may also be a moiety such as silver, tropylium, carboniums, ferroceniums and mixtures, preferably carboniums and ferroceniums. Most preferably Z d + is triphenyl carbonium.
  • Preferred reducible Lewis acids can be any triaryl carbonium (where the aryl can be substituted or unsubstituted, such as those represented by the formula: (Ar 3 C + ), where Ar is aryl or aryl substituted with a heteroatom, a to C 40 hydrocarbyl, or a substituted CI to C40 hydrocarbyl), preferably the reducible Lewis acids in formula (14) above as "Z" include those represented by the formula: (Ph 3 C), where Ph is a substituted or unsubstituted phenyl, preferably substituted with to C 40 hydrocarbyls or substituted a C j to C40 hydrocarbyls, preferably Cj to C 2Q alkyls or aromatics or substituted Cj to C 2Q alky IS or aromatics, preferably Z is a triphenylcarbonium.
  • the aryl can be substituted or unsubstituted, such as those represented by the formula: (Ar 3 C + ), where Ar is aryl or
  • Z d + is the activating cation (L-H) d + , it is preferably a Bronsted acid, capable of donating a proton to the transition metal catalytic precursor resulting in a transition metal cation, including ammoniums, oxoniums, phosphoniums, silyliums, and mixtures thereof, preferably ammoniums of methylamine, aniline, dimethylamine, diethylamine, N- methylaniline, diphenylamine, trimethylamine, triethylamine, N,N-dimethylaniline, methyldiphenylamine, pyridine, p-bromo N,N-dimethylaniline, p-nitro-N,N-dimethylaniline, phosphoniums from triethylphosphine, triphenylphosphine, and diphenylphosphine, oxomiuns from ethers such as dimethyl ether diethyl ether, tetra
  • the anion component A d" includes those having the formula [M k+ Q n ] d_ wherein k is 1,
  • each Q is a fluorinated hydrocarbyl group having 1 to 20 carbon atoms, more preferably each Q is a fluorinated aryl group, and most preferably each Q is a pentafluoryl aryl group.
  • suitable A d also include diboron compounds as disclosed in US 5,447,895, which is fully incorporated herein by reference.
  • boron compounds which may be used as an activating cocatalyst are the compounds described as (and particularly those specifically listed as) activators in US 8,658,556, which is incorporated by reference herein.
  • the ionic stoichiometric activator Z d + (A d_ ) is one or more of N,N- dimethylanilinium tetra(perfluorophenyl)borate, N,N-dimethylanilinium tetrakis(perfluoronaphthyl)borate, N,N-dimethylanilinium tetrakis(perfluorobiphenyl)borate, N,N-dimethylanilinium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluoronaphthyl)borate, triphenylcarbenium tetrakis(perfluorobiphenyl)borate, triphenylcarbenium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, or triphenylcarbenium tetra(perfluorophen
  • each is, independently, a halide, preferably a fluoride
  • Ar is substituted or unsubstituted aryl group (preferably a substituted or unsubstituted phenyl), preferably substituted with to C 40 hydrocarbyls, preferably to C 2 o alky Is or aromatics;
  • each R 2 is, independently, a halide, a C 6 to C 20 substituted aromatic hydrocarbyl group or a siloxy group of the formula -0-Si-R a , where R a is a to C 20 hydrocarbyl or hydrocarbylsilyl group (preferably R 2 is a fluoride or a perfluorinated phenyl group);
  • each R 3 is a halide, C 6 to C 20 substituted aromatic hydrocarbyl group or a siloxy group of the formula -0-Si-R a , where R a is a to C 20 hydrocarbyl or hydrocarbylsilyl group (preferably R 3 is a fluoride or a C 6 perfluorinated aromatic hydrocarbyl group); wherein R 2 and R 3 can form one or more saturated or unsaturated, substituted or unsubstituted rings (preferably R 2 and R 3 form a perfluorinated phenyl ring); and
  • L is a neutral Lewis base
  • (L-H) + is a Bronsted acid
  • d is 1, 2, or 3;
  • the anion has a molecular weight of greater than 1020 g/mol
  • ( ⁇ 3 (3 ⁇ 4 + is (Ph 3 C) cl + , where Ph is a substituted or unsubstituted phenyl, preferably substituted with to C 40 hydrocarbyls or substituted to C 40 hydrocarbyls, preferably to C 2Q alkyls or aromatics or substituted to C 2Q alkyls or aromatics.
  • Molecular volume is used herein as an approximation of spatial steric bulk of an activator molecule in solution. Comparison of substituents with differing molecular volumes allows the substituent with the smaller molecular volume to be considered “less bulky” in comparison to the substituent with the larger molecular volume. Conversely, a substituent with a larger molecular volume may be considered “more bulky” than a substituent with a smaller molecular volume. Molecular volume may be calculated as reported in "A Simple "Back of the Envelope” Method for Estimating the Densities and Molecular Volumes of Liquids and Solids," Journal of Chemical Education, Vol. 71, No. 11, November 1994, pp. 962-964.
  • MV Molecular volume
  • V s the scaled volume.
  • V s the sum of the relative volumes of the constituent atoms, and is calculated from the molecular formula of the substituent using the following table of relative volumes. For fused rings, the V s is decreased by 7.5% per fused ring.
  • one or more of the NCA activators is chosen from the activators described in US 6,211 , 105.
  • Preferred activators include N,N-dimethylanilinium tetrakis(perfluoronaphthyl)borate, N,N-dimethylanilinium tetrakis(perfluorobiphenyl)borate, N,N-dimethylanilinium tetrakis(perfluorophenyl)borate, N,N-dimethylanilinium tetrakis(3,5- bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluoronaphthyl)borate, triphenylcarbenium tetrakis(perfluorobiphenyl)borate, triphenylcarbenium tetrakis(3,5- bis(trifluoromethyl)phenyl)borate, triphenylcarbenium tetrakis(perfluorophenyl)borate, [Ph 3 C+] [B(C 6 F 5 ) 4
  • the activator comprises a triaryl carbonium (such as triphenylcarbenium tetraphenylborate, triphenylcarbenium tetrakis(pentafluorophenyl)borate, triphenylcarbenium tetrakis-(2,3,4,6-tetrafluorophenyl)borate, triphenylcarbenium tetrakis(perfluoronaphthyl)borate, triphenylcarbenium tetrakis(perfluorobiphenyl)borate, triphenylcarbenium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate).
  • a triaryl carbonium such as triphenylcarbenium tetraphenylborate, triphenylcarbenium tetrakis(pentafluorophenyl)borate, triphenylcarbenium tetrakis-(2,3,4,6-tetra
  • the activator comprises one or more of trialkylammonium tetrakis(pentafluorophenyl)borate, N,N-dialkylanilinium tetrakis(pentafluorophenyl)borate, N,N-dimethyl-(2,4,6-trimethylanilinium) tetrakis(pentafluorophenyl)borate, trialkylammonium tetrakis-(2,3,4,6-tetrafluorophenyl) borate, N,N-dialkylanilinium tetrakis- (2,3,4,6-tetrafluorophenyl)borate, trialkylammonium tetrakis(perfluoronaphthyl)borate, N,N- dialkylanilinium tetrakis(perfluoronaphthyl)borate, trialkylammonium tetrakis(perfluorobiphenyl)borate,
  • the typical activator-to-catalyst ratio e.g., all NCA activators-to-catalyst ratio is about a 1 : 1 molar ratio.
  • Alternate preferred ranges include from 0.1 : 1 to 100: 1, alternately from 0.5: 1 to 200: 1, alternately from 1 : 1 to 500: 1 , alternately from 1 : 1 to 1000: 1.
  • a particularly useful range is from 0.5 : 1 to 10: 1, preferably 1 : 1 to 5 : 1.
  • the catalyst compounds can be combined with combinations of alumoxanes and NCA's (see for example, US 5,153, 157; US 5,453,410; EP 0 573 120 Bl ; WO 94/07928; and WO 95/14044 which discuss the use of an alumoxane in combination with an ionizing activator).
  • Useful chain transfer agents are typically alkylalumoxanes, a compound represented by the formula A1R 3 , ZnR 2 (where each R is, independently, a Ci-Cg aliphatic radical, preferably methyl, ethyl, propyl, butyl, pentyl, hexyl octyl or an isomer thereof) or a combination thereof, such as diethyl zinc, methylalumoxane, trimethylaluminum, triisobutylaluminum, trioctylaluminum, or a combination thereof.
  • Aluminum alkyl or organoaluminum compounds which may be utilized as scavengers or co-activators include, for example, trimethylaluminum, triethylaluminum, triisobutylaluminum, tri-n-hexylaluminum, tri-n-octylaluminum, and diethyl zinc.
  • the catalyst system may comprise an inert support material.
  • the supported material is a porous support material, for example, talc, and inorganic oxides.
  • Other support materials include zeolites, clays, organoclays, or any other organic or inorganic support material and the like, or mixtures thereof.
  • the support material is an inorganic oxide in a finely divided form.
  • Suitable inorganic oxide materials for use in metallocene catalyst systems herein include Groups 2, 4, 13, and 14 metal oxides, such as silica, alumina, and mixtures thereof.
  • Other inorganic oxides that may be employed either alone or in combination with the silica, or alumina are magnesia, titania, zirconia, and the like.
  • suitable support materials can be employed, for example, finely divided functionalized polyolefins, such as finely divided polyethylene.
  • Particularly useful supports include magnesia, titania, zirconia, montmorillonite, phyllosilicate, zeolites, talc, clays, and the like.
  • support materials may be used, for example, silica-chromium, silica-alumina, silica-titania, and the like.
  • Preferred support materials include A1 2 0 3 , Zr0 2 , Si0 2 , and combinations thereof, more preferably Si0 2 , A1 2 0 3 , or Si0 2 /Al 2 0 3.
  • the support material most preferably an inorganic oxide, has a surface area in the range of from about 10 to about 700 m 2 /g, pore volume in the range of from about 0.1 to about 4.0 cc/g and average particle size in the range of from about 5 to about 500 ⁇ . More preferably, the surface area of the support material is in the range of from about 50 to about 500 m 2 /g, pore volume of from about 0.5 to about 3.5 cc/g and average particle size of from about 10 to about 200 ⁇ .
  • the surface area of the support material is in the range is from about 100 to about 400 m 2 /g, pore volume from about 0.8 to about 3.0 cc/g and average particle size is from about 5 to about 100 ⁇ .
  • the average pore size of the support material useful in the invention is in the range of from 10 to 1000 A, preferably 50 to about 500 A, and most preferably 75 to about 350 A.
  • Preferred silicas are marketed under the tradenames of DAVISON 952 or DAVISON 955 by the Davison Chemical Division of W.R. Grace and Company. In other embodiments DAVISON 948 is used.
  • the support material should be dry, that is, free of absorbed water. Drying of the support material can be effected by heating or calcining at about 100°C to about 1000°C, preferably at least about 600°C. When the support material is silica, it is heated to at least 200°C, preferably about 200°C to about 850°C, and most preferably at about 600°C; and for a time of about 1 minute to about 100 hours, from about 12 hours to about 72 hours, or from about 24 hours to about 60 hours.
  • the calcined support material must have at least some reactive hydroxyl (OH) groups to produce supported catalyst systems of this invention.
  • the calcined support material is then contacted with at least one polymerization catalyst comprising at least one metallocene compound and an activator.
  • the support material having reactive surface groups, typically hydroxyl groups, is slurried in a non-polar solvent and the resulting slurry is contacted with a solution of a metallocene compound and an activator.
  • the slurry of the support material is first contacted with the activator for a period of time in the range of from about 0.5 hrs. to about 24 hrs., from about 2 hrs. to about 16 hrs., or from about 4 hrs. to about 8 hrs.
  • the solution of the metallocene compound is then contacted with the isolated support/activator.
  • the supported catalyst system is generated in situ.
  • the slurry of the support material is first contacted with the catalyst compound for a period of time in the range of from about 0.5 hrs. to about 24 hrs., from about 2 hrs. to about 16 hrs., or from about 4 hrs. to about 8 hrs.
  • the slurry of the supported metallocene compound is then contacted with the activator solution.
  • the mixture of the metallocene, activator and support is heated to about 0°C to about 70°C, preferably to about 23°C to about 60°C, preferably at room temperature.
  • Contact times typically range from about 0.5 hrs. to about 24 hrs., from about 2 hrs. to about 16 hrs., or from about 4 hrs. to about 8 hrs.
  • Suitable non-polar solvents are materials in which all of the reactants used herein, i.e., the activator, and the metallocene compound, are at least partially soluble and which are liquid at reaction temperatures.
  • Preferred non-polar solvents are alkanes, such as isopentane, hexane, n-heptane, octane, nonane, and decane, although a variety of other materials including cycloalkanes, such as cyclohexane, aromatics, such as benzene, toluene, and ethylbenzene, may also be employed.
  • this invention uses a flourided (also referred to as flouridated) support.
  • the flourided supports (such as flourided silica) can be obtained through the addition of a solution of polar solvent (such as water) and fluorine compound (such as NH 4 ) 2 SiF 6 ) to a slurry of support (such as a toluene slurry of silica).
  • a slurry of support such as a toluene slurry of silica.
  • This preparation method contributes to an even distribution of the fluoride compound (such as (NH 4 ) 2 SiF 6 ) onto the support surface (such as the silica surface), in contrast to a less homogeneous distribution observed when the solid salt is combined with the solid silica as described in US 2002/0123582 Al.
  • an aqueous solution of fluorinating agent such as (NH ⁇ SiFe) is added to a slurry of support (such as a toluene slurry of silica). Vigorous stirring of the mixture allows the dissolved fluorine compound (in water) to be evenly absorbed onto the hydrophilic support surface. After filtration, the wet support is allowed to air dry until it is free flowing, and then may be calcined (typically at temperatures over 100°C for at least 1 hr.).
  • fluorinating agent such as (NH ⁇ SiFe)
  • a slurry of support such as a toluene slurry of silica. Vigorous stirring of the mixture allows the dissolved fluorine compound (in water) to be evenly absorbed onto the hydrophilic support surface. After filtration, the wet support is allowed to air dry until it is free flowing, and then may be calcined (typically at temperatures over 100°C for at least 1 hr.).
  • a solution of polar solvent and fluorinating agent such as NH4)2SiF6
  • a slurry of support such as a toluene slurry of silica
  • Vigorous stirring of the mixture allows the dissolved fluorine compound (in water) to be evenly absorbed onto the hydrophilic support surface.
  • the wet support is allowed to air dry until it is free flowing, and then may be calcined (typically at temperatures over 100°C for at least 1 hr.).
  • the catalyst systems described herein are prepared by:
  • Fluorided silica preparation typically employs a minimal amount of a polar solvent (e.g., water, methanol, ethanol, isopropanol, or any solvent capable of dissolving the fluoride compound (such as ammonium hexafluorosilicate)) to dissolve the fluorinating agent (such as ammonium hexafluorosilicate), but can use an excess of solvent if desired.
  • a polar solvent e.g., water, methanol, ethanol, isopropanol, or any solvent capable of dissolving the fluoride compound (such as ammonium hexafluorosilicate)
  • the solution typically ammonium hexafluorosilicate solution
  • a non-polar solvent e.g., toluene, or benzene, chloroform, etc.
  • fluorinating agent such as ammonium hexafluorosilicate
  • hydrophilic silica surface When the non-polar solvent is removed (by filtration), silica with an even distribution of fluorinating agent (such as ammonium hexafluorosilicate) is obtained, and ready for subsequent drying and calcination steps.
  • alumoxane such as methylalumoxane
  • the fluorided support material is then slurried in a non-polar solvent and the resulting slurry is contacted with a solution of alumoxane (such as methylalumoxane).
  • alumoxane such as methylalumoxane
  • the fluorided support/alumoxane mixture is then heated to elevated temperature (30°C to 120°C, preferably, 80-100°C) with vigorous stirring for a period of time (0.1 to 24 hrs., preferably, 1 to 3 hrs.).
  • the support/activator is isolated by filtration, rinsed with non-polar solvent (e.g., toluene, pentane, hexane, etc.), and dried.
  • non-polar solvent e.g., toluene, pentane, hexane, etc.
  • the isolated support/activator is then slurried in a non-polar solvent (e.g., toluene), and a solution of metallocene compound/compounds is then contacted with the support/activator slurry. Vigorous stirring is typically applied.
  • the fluorided support material may be slowly added in solid form to a solution of alumoxane in non-polar solvent (e.g., toluene) (typically at room temperature) with vigorous stirring.
  • alumoxane in non-polar solvent (e.g., toluene) (typically at room temperature)
  • This addition sequence namely slow and portion-wise addition of fluorided silica to the alumoxane solution, is referred to as "reversed addition”.
  • the fluorided support/alumoxane mixture is then heated to elevated temperature (30°C to 120°C, preferably, 80 to 100°C) with vigorous stirring for a period of time (0.1 to 24 hrs., preferably, 1 to 3 hrs.).
  • the support/activator is then isolated by filtration, rinsed with non-polar solvent (e.g., toluene, pentane, hexane, etc.), and dried.
  • the isolated support/activator is then slurried in a non-polar solvent (e.g., toluene), and a solution of metallocene compound/compounds is then contacted with the support/activator slurry.
  • Vigorous stirring is typically applied.
  • the reversed addition method for immobilizing MAO on fluorided silica surface offers higher polymerization activity for a wide variety of catalysts, compared to the "traditional addition” method where methylalumoxane solution is added to a slurry of fluorided silica in non-polar solvent.
  • the silica/MAO support/activator generated in the MAO immobilization step 2 (a or b) is slurried in a non- polar solvent (e.g., toluene).
  • a non- polar solvent e.g., toluene
  • the resulting slurry is then contacted with a solution of metallocene (one metallocene precursor or more) with vigorous stirring.
  • the mixture is stirred for 0.5 hr. to 24 hrs. (preferably, for 1 to 3 hrs.) at a temperature between 23°C to 110°C (preferably, at 20°C to 40°C).
  • the finished supported catalyst is then isolated by filtration, rinsed with non-polar solvent (e.g., toluene, pentane), and dried.
  • the metallocene precursors can be dissolved together with solvent to create one solution, or each metallocene can be dissolved individually.
  • the metallocene precursor(s) can be added to silica/alumoxane support/activator slurry together in one solution, or individual solutions of each metallocene precursor can be added in any order/sequence. In a preferred embodiment of the invention, multiple metallocene precursor(s) are added to silica/alumoxane support/activator slurry together in one solution.
  • the invention relates to polymerization processes where monomer (such as propylene), and optionally comonomer, are contacted with a catalyst system comprising an activator and at least one metallocene compound, as described above.
  • monomer such as propylene
  • a catalyst system comprising an activator and at least one metallocene compound, as described above.
  • the catalyst compound and activator may be combined in any order, and are combined typically prior to contacting with the monomer.
  • Monomers useful herein include substituted or unsubstituted C 2 to C40 alpha olefins, preferably C 2 to C 20 alpha olefins, preferably C 2 to C 12 alpha olefins, preferably ethylene, propylene, butene, pentene, hexene, heptene, octene, nonene, decene, undecene, dodecene and isomers thereof.
  • the monomer comprises propylene and an optional comonomers comprising one or more ethylene or C 4 to C 40 olefins, preferably C 4 to C 20 olefins, or preferably C 6 to C 12 olefins.
  • the C 4 to C 40 olefin monomers may be linear, branched, or cyclic.
  • the C 4 to C 40 cyclic olefins may be strained or unstrained, monocyclic or polycyclic, and may optionally include heteroatoms and/or one or more functional groups.
  • the monomer comprises ethylene and an optional comonomers comprising one or more C 3 to C 40 olefins, preferably C 4 to C 20 olefins, or preferably C 6 to C 12 olefins.
  • the C 3 to C 40 olefin monomers may be linear, branched, or cyclic.
  • the C3 to C 4Q cyclic olefins may be strained or unstrained, monocyclic or polycyclic, and may optionally include heteroatoms and/or one or more functional groups.
  • Exemplary C 2 to C 4Q olefin monomers and optional comonomers include ethylene, propylene, butene, pentene, hexene, heptene, octene, nonene, decene, undecene, dodecene, norbornene, norbornadiene, dicyclopentadiene, cyclopentene, cycloheptene, cyclooctene, cyclooctadiene, cyclododecene, 7-oxanorbornene, 7-oxanorbornadiene, substituted derivatives thereof, and isomers thereof, preferably hexene, heptene, octene, nonene, decene, dodecene, cyclooctene, 1,5-cyclooctadiene, 1 -hydroxy -4-cyclooctene, l-acetoxy-4- cyclooctene,
  • one or more dienes are present in the polymer produced herein at up to 10 wt%, preferably at 0.00001 to 1.0 wt%, preferably 0.002 to 0.5 wt%, even more preferably 0.003 to 0.2 wt%, based upon the total weight of the composition.
  • 500 ppm or less of diene is added to the polymerization, preferably 400 ppm or less, preferably or 300 ppm or less.
  • at least 50 ppm of diene is added to the polymerization, or 100 ppm or more, or 150 ppm or more.
  • Preferred diolefin monomers useful in this invention include any hydrocarbon structure, preferably C4 to C30, having at least two unsaturated bonds, wherein at least two of the unsaturated bonds are readily incorporated into a polymer by either a stereospecific or a non- stereospecific catalyst(s). It is further preferred that the diolefin monomers be selected from alpha, omega-diene monomers (i.e., di-vinyl monomers). More preferably, the diolefin monomers are linear di-vinyl monomers, most preferably, those containing from 4 to 30 carbon atoms.
  • Examples of preferred dienes include butadiene, pentadiene, hexadiene, heptadiene, octadiene, nonadiene, decadiene, undecadiene, dodecadiene, tridecadiene, tetradecadiene, pentadecadiene, hexadecadiene, heptadecadiene, octadecadiene, nonadecadiene, icosadiene, heneicosadiene, docosadiene, tricosadiene, tetracosadiene, pentacosadiene, hexacosadiene, heptacosadiene, octacosadiene, nonacosadiene, triacontadiene, particularly preferred dienes include 1 ,6-heptadiene, 1,7-octadiene, 1 ,8- nonadiene, 1 ,9
  • Preferred cyclic dienes include cyclopentadiene, vinylnorbomene, norbornadiene, ethylidene norbornene, divinylbenzene, dicyclopentadiene or higher ring containing diolefins with or without substituents at various ring positions.
  • Polymerization processes of this invention can be carried out in any manner known in the art. Any suspension, homogeneous, bulk, solution, slurry, or gas phase polymerization process known in the art can be used. Such processes can be run in a batch, semi-batch, or continuous mode. Homogeneous polymerization processes and slurry processes are preferred. (A homogeneous polymerization process is defined to be a process where at least 90 wt% of the product is soluble in the reaction media.) A bulk homogeneous process is particularly preferred.
  • a bulk process is defined to be a process where monomer concentration in all feeds to the reactor is 70 volume % or more.
  • no solvent or diluent is present or added in the reaction medium, (except for the small amounts used as the carrier for the catalyst system or other additives, or amounts typically found with the monomer; e.g., propane in propylene).
  • the process is a slurry process.
  • slurry polymerization process means a polymerization process where a supported catalyst is employed and monomers are polymerized on the supported catalyst particles. At least 95 wt% of polymer products derived from the supported catalyst are in granular form as solid particles (not dissolved in the diluent).
  • Suitable diluents/solvents for polymerization include non-coordinating, inert liquids.
  • Examples include straight and branched-chain hydrocarbons, such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof; cyclic and alicyclic hydrocarbons, such as cyclohexane, cycloheptane, methylcyclohexane, methylcycloheptane, and mixtures thereof, such as can be found commercially (IsoparTM); perhalogenated hydrocarbons, such as perfiuorinated C 4 .
  • straight and branched-chain hydrocarbons such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof
  • cyclic and alicyclic hydrocarbons such as cyclohexane,
  • Suitable solvents also include liquid olefins which may act as monomers or comonomers including ethylene, propylene, 1-butene, 1-hexene, 1-pentene, 3 -methyl- 1- pentene, 4-methyl- 1-pentene, 1-octene, 1-decene, and mixtures thereof.
  • aliphatic hydrocarbon solvents are used as the solvent, such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof; cyclic and alicyclic hydrocarbons, such as cyclohexane, cycloheptane, methylcyclohexane, methylcycloheptane, and mixtures thereof.
  • the solvent is not aromatic, preferably aromatics are present in the solvent at less than 1 wt%, preferably less than 0.5 wt%, preferably less than 0 wt% based upon the weight of the solvents.
  • the feed concentration of the monomers and comonomers for the polymerization is 60 vol% solvent or less, preferably 40 vol% or less, or preferably 20 vol% or less, based on the total volume of the feedstream.
  • the polymerization is run in a bulk process.
  • Preferred polymerizations can be run at any temperature and/or pressure suitable to obtain the desired ethylene polymers.
  • Typical temperatures and/or pressures include a temperature in the range of from about 0°C to about 300°C, preferably about 20°C to about 200°C, preferably about 35°C to about 150°C, preferably from about 40°C to about 120°C, preferably from about 45°C to about 80°C; and at a pressure in the range of from about 0.35 MPa to about 10 MPa, preferably from about 0.45 MPa to about 6 MPa, or preferably from about 0.5 MPa to about 4 MPa.
  • the run time of the reaction is up to 300 minutes, preferably in the range of from about 5 to 250 minutes, or preferably from about 10 to 120 minutes.
  • hydrogen is present in the polymerization reactor at a partial pressure of 0.001 to 50 psig (0.007 to 345 kPa), preferably from 0.01 to 25 psig (0.07 to 172 kPa), more preferably 0.1 to 10 psig (0.7 to 70 kPa).
  • the activity of the catalyst is at least 50 g/mmol/hour, preferably 500 or more g/mmol/hour, preferably 5000 or more g/mmol/hr, preferably 50,000 or more g/mmol/hr.
  • the conversion of olefin monomer is at least 10%, based upon polymer yield and the weight of the monomer entering the reaction zone, preferably 20% or more, preferably 30% or more, preferably 50% or more, preferably 80% or more.
  • alumoxane is present at zero mol%, alternately the alumoxane is present at a molar ratio of aluminum to transition metal less than 500: 1, preferably less than 300: 1 , preferably less than 100: 1 , preferably less than 1 : 1.
  • scavenger such as tri alkyl aluminum
  • the scavenger is present at zero mol%, alternately the scavenger is present at a molar ratio of scavenger metal to transition metal of less than 100: 1, preferably less than 50: 1 , preferably less than 15 : 1 , preferably less than 10: 1.
  • the polymerization 1) is conducted at temperatures of 0 to 300°C (preferably 25 to 150°C, preferably 40 to 120°C, preferably 45 to 80°C); 2) is conducted at a pressure of atmospheric pressure to 10 MPa (preferably 0.35 to 10 MPa, preferably from 0.45 to 6 MPa, preferably from 0.5 to 4 MPa); 3) is conducted in an aliphatic hydrocarbon solvent (such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof; cyclic and alicyclic hydrocarbons, such as cyclohexane, cycloheptane, methylcyclohexane, methylcycloheptane, and mixtures thereof; preferably where aromatics are preferably present in the solvent at less than 1 wt%, preferably less than 0.5 wt%, preferably at 0 w
  • the catalyst system used in the polymerization comprises no more than one catalyst compound.
  • a "reaction zone” also referred to as a “polymerization zone” is a vessel where polymerization takes place, for example, a batch reactor. When multiple reactors are used in either series or parallel configuration, each reactor is considered as a separate polymerization zone. For a multi- stage polymerization in both a batch reactor and a continuous reactor, each polymerization stage is considered as a separate polymerization zone. In a preferred embodiment, the polymerization occurs in one reaction zone. Room temperature is 23°C unless otherwise noted.
  • additives may also be used in the polymerization, as desired, such as one or more scavengers, promoters, modifiers, chain transfer agents (such as diethyl zinc), reducing agents, oxidizing agents, hydrogen, aluminum alkyls, or silanes.
  • Useful chain transfer agents are typically alkylalumoxanes, a compound represented by the formula A1R 3 , ZnR 2 (where each R is, independently, a Ci-Cg aliphatic radical, preferably methyl, ethyl, propyl, butyl, pentyl, hexyl, octyl or an isomer thereof) or a combination thereof, such as diethyl zinc, methylalumoxane, trimethylaluminum, triisobutylaluminum, trioctylaluminum, or a combination thereof.
  • This invention also relates to compositions of matter produced by the methods described herein.
  • the process described herein produces C2 to C20 olefin homopolymers or copolymers, such as ethylene-hexene, propylene-ethylene and/or propylene-alphaolefin (preferably C3 to C20) copolymers (such as propylene-hexene copolymers or propylene-octene copolymers) having low comonomer incorporation (such as low C6 wt%) and/or broad molecular weight distribution (MWD).
  • C2 to C20 olefin homopolymers or copolymers such as ethylene-hexene, propylene-ethylene and/or propylene-alphaolefin (preferably C3 to C20) copolymers (such as propylene-hexene copolymers or propylene-octene copolymers) having low comonomer incorporation (such as low C6 wt%) and/or broad molecular weight distribution (MWD).
  • the process of this invention produces olefin polymers, preferably polyethylene and polypropylene homopolymers and copolymers.
  • the polymers produced herein are homopolymers of ethylene or copolymers of ethylene preferably having from 0 to 25 mol% (alternately from 0.5 to 20 mol%, alternately from 1 to 15 mol%, preferably from 3 to 10 mol%) of one or more C3 to C20 olefin comonomer (preferably C3 to C 12 alpha-olefin, preferably propylene, butene, hexene, octene, decene, dodecene, preferably propylene, butene, hexene, octene).
  • the polymers produced herein are homopolymers of propylene or are copolymers of propylene preferably having from 0 to 25 mol% (alternately from 0.5 to 20 mol%, alternately from 1 to 15 mol%, preferably from 3 to 10 mol%) of one or more of C2 or C4 to C20 olefin comonomer (preferably ethylene or C4 to C 12 alpha-olefin, preferably ethylene, butene, hexene, octene, decene, dodecene, preferably ethylene, butene, hexene, octene).
  • C2 or C4 to C20 olefin comonomer preferably ethylene or C4 to C 12 alpha-olefin, preferably ethylene, butene, hexene, octene, decene, dodecene, preferably ethylene, butene, hexene, octene.
  • the monomer is ethylene and the comonomer is hexene, preferably from 0.5 to 15 mol% hexene, alternately 1 to 10 mol%.
  • the polymers produced herein have an Mw of 20,000 to 1,000,000 g/mol (preferably 60,000 to 300,000 g/mol), and/or an Mw/Mn of greater than 1 to 40 (alternately 1.2 to 20, alternately 1.3 to 10, alternately 1.4 to 8, alternately 1.5 to 6, alternately 2 to 6).
  • the polymer produced herein has a unimodal or multimodal molecular weight distribution as determined by Gel Permeation Chromatography (GPC).
  • GPC Gel Permeation Chromatography
  • unimodal is meant that the GPC trace has one peak or inflection point.
  • multimodal is meant that the GPC trace has at least two peaks or inflection points.
  • An inflection point is that point where the second derivative of the curve changes in sign (e.g., from negative to positive or vice versus).
  • the polymer (preferably the polyethylene or polypropylene) produced herein is combined with one or more additional polymers prior to being formed into a film, molded part or other article.
  • additional polymers include polyethylene, isotactic polypropylene, highly isotactic polypropylene, syndiotactic polypropylene, random copolymer of propylene and ethylene, and/or butene, and/or hexene, polybutene, ethylene vinyl acetate, LDPE, LLDPE, HDPE, ethylene vinyl acetate, ethylene methyl acrylate, copolymers of acrylic acid, polymethylmethacrylate or any other polymers polymerizable by a high-pressure free radical process, polyvinylchloride, polybutene- 1, isotactic polybutene, ABS resins, ethylene-propylene rubber (EPR), vulcanized EPR, EPDM, block copolymer, styrenic block copolymers, poly
  • the polymer (preferably the polyethylene or polypropylene) is present in the above blends, at from 10 to 99 wt%, based upon the weight of the polymers in the blend, preferably 20 to 95 wt%, even more preferably at least 30 to 90 wt%, even more preferably at least 40 to 90 wt%, even more preferably at least 50 to 90 wt%, even more preferably at least 60 to 90 wt%, even more preferably at least 70 to 90 wt%.
  • the blends described above may be produced by mixing the polymers of the invention with one or more polymers (as described above), by connecting reactors together in series to make reactor blends or by using more than one catalyst in the same reactor to produce multiple species of polymer.
  • the polymers can be mixed together prior to being put into the extruder or may be mixed in an extruder.
  • the blends may be formed using conventional equipment and methods, such as by dry blending the individual components and subsequently melt mixing in a mixer, or by mixing the components together directly in a mixer, such as, for example, a Banbury mixer, a Haake mixer, a Brabender internal mixer, or a single or twin-screw extruder, which may include a compounding extruder and a side-arm extruder used directly downstream of a polymerization process, which may include blending powders or pellets of the resins at the hopper of the film extruder. Additionally, additives may be included in the blend, in one or more components of the blend, and/or in a product formed from the blend, such as a film, as desired.
  • a mixer such as, for example, a Banbury mixer, a Haake mixer, a Brabender internal mixer, or a single or twin-screw extruder, which may include a compounding extruder and a side-arm extruder used directly downstream of a polymerization
  • additives are well known in the art, and can include, for example: fillers; antioxidants (e.g., hindered phenolics such as IRGANOXTM 1010 or IRGANOXTM 1076 available from Ciba- Geigy); phosphites (e.g., IRGAFOSTM 168 available from Ciba-Geigy); anti-cling additives; tackifiers, such as polybutenes, terpene resins, aliphatic and aromatic hydrocarbon resins, alkali metal and glycerol stearates, and hydrogenated rosins; UV stabilizers; heat stabilizers; anti-blocking agents; release agents; anti-static agents; pigments; colorants; dyes; waxes; silica; fillers; talc; and the like.
  • antioxidants e.g., hindered phenolics such as IRGANOXTM 1010 or IRGANOXTM 1076 available from Ciba- Geig
  • any of the foregoing polymers such as the foregoing polyethylenes or blends thereof, may be used in a variety of end-use applications.
  • Such applications include, for example, mono- or multi-layer blown, extruded, and/or shrink films.
  • These films may be formed by any number of well known extrusion or coextrusion techniques, such as a blown bubble film processing technique, wherein the composition can be extruded in a molten state through an annular die and then expanded to form a uni-axial or biaxial orientation melt prior to being cooled to form a tubular, blown film, which can then be axially slit and unfolded to form a flat film.
  • Films may be subsequently unoriented, uniaxially oriented, or biaxially oriented to the same or different extents.
  • One or more of the layers of the film may be oriented in the transverse and/or longitudinal directions to the same or different extents.
  • the uniaxial orientation can be accomplished using typical cold drawing or hot drawing methods.
  • Biaxial orientation can be accomplished using tenter frame equipment or a double bubble process and may occur before or after the individual layers are brought together.
  • a polyethylene layer can be extrusion coated or laminated onto an oriented polypropylene layer or the polyethylene and polypropylene can be coextruded together into a film then oriented.
  • oriented polypropylene could be laminated to oriented polyethylene or oriented polyethylene could be coated onto polypropylene then optionally the combination could be oriented even further.
  • the films are oriented in the Machine Direction (MD) at a ratio of up to 15, preferably between 5 and 7, and in the Transverse Direction (TD) at a ratio of up to 15, preferably 7 to 9.
  • MD Machine Direction
  • TD Transverse Direction
  • the film is oriented to the same extent in both the MD and TD directions.
  • the films may vary in thickness depending on the intended application; however, films of a thickness from 1 to 50 ⁇ are usually suitable. Films intended for packaging are usually from 10 to 50 ⁇ thick.
  • the thickness of the sealing layer is typically 0.2 to 50 ⁇ .
  • one or more layers may be modified by corona treatment, electron beam irradiation, gamma irradiation, flame treatment, or microwave.
  • one or both of the surface layers is modified by corona treatment.
  • M 1 is selected from the group consisting of titanium, zirconium, hafnium; each R 1 and R 2 are identical or different and are each a hydrogen atom, a Ci-Cio alkyl group, a Ci-Cio alkoxy group, a C6-C 10 aryl group, a C6-C 10 aryloxy group, a C 2 -C 10 alkenyl group, a C 2 -C40 alkenyl group, a C7-C40 arylalkyl group, a C7-C40 alkylaryl group, a C8-C40 (preferably C8-C30) arylalkenyl group, an OH group or a halogen atom, or a conjugated diene which is optionally substituted with one or more hydrocarbyl, tri (hydrocarbyl) silyl groups or tri (hydrocarbyl) silylhydrocarbyl groups, said diene having up to 30 atoms not counting hydrogen;
  • each R 3 to R 7 are identical or different and are each a hydrogen atom, or a substituted or unsubstituted, branched or unbranched C1-C10 alkyl group;
  • R 13 is -((R 15 *) 2 Si-Si(R 15 ) 2 )- wherein, each R 15 and R 15 * is identical or different and is a substituted or unsubstituted, branched or unbranched C 1 -C 20 alkyl group, where preferably, each R 15 together do not form a ring, and/or each R 15 * together do not form a ring, and/or R 15 and R together do not form a ring;
  • each R 8 , R 10 and R 12 are identical or different and are each a hydrogen atom or a substituted or unsubstituted, branched or unbranched Ci-Cio alkyl group;
  • each R 9 and R 11 are identical or different and are a hydrogen atom or a substituted or unsubstituted, branched or unbranched C2-C20 alkyl group is presented.
  • each R 3 is a hydrogen atom or a C1-C10 alkyl group
  • R 8 , R 10 and R 12 are each hydrogen atoms
  • each R 9 and R 11 are identical or different and are each a C3-C20 alkyl group.
  • each R 3 is a hydrogen atom and each R 9 and R 11 are each t-butyl groups.
  • a catalyst system comprising activator and the catalyst compound of any of paragraphs 1 to 8.
  • a process to polymerize ethylene comprising contacting ethylene and, optionally, one or more olefin comonomers, with the catalyst compound of any of paragraphs 1-8 or catalyst system of paragraph 9; wherein the polymer produced has at least 50 mol% ethylene and an M w between 20,000 g/mol and 400,000 g/mol.
  • Z is (L-H) or a reducible Lewis Acid
  • L is a neutral Lewis base
  • H is hydrogen
  • (L- H)+ is a Bronsted acid
  • Ad- is a non-coordinating anion having the charge d-
  • d is an integer from 1 to 3.
  • Ad- is a non-coordinating anion having the charge d-; d is an integer from 1 to 3, and Z is a reducible Lewis acid represented by the formula: (Ar3C+), where Ar is aryl or aryl substituted with a heteroatom, a Ci to C40 hydrocarbyl, or a substituted Ci to C40 hydrocarbyl.
  • N,N-diethylanilinium tetrakis(perfluoronaphthyl)borate N,N-diethylanilinium tetrakis(perfluoronaphthyl)borate.
  • D948 also referred to as Davison 948, is Silica SYLOPOLTM 948, available from WR Grace and Company, Columbia, Maryland, USA.
  • Catalyst 1 is D948 supported meso-tetramethyldisilylene bis(4-(3',5'-di-tert- butylphenyl)-indenyl) zirconium dichloride using procedure A.
  • Catalyst 2 is a supported catalyst made in a manner analogous to that described in US 6,180,736 using the (l-Me-3-"BuCp) 2 ZrCl 2 metallocene.
  • Catalyst 3 is D948 supported rac-dimethylsilylbis (2-methyl-4-phenyl indenyl)
  • Catalyst 4 is D948 supported raodimethylsilyl bis(2-cyclopropyl-4-(3',5'-di-tert- butylphenyl)-indenyl) ZrCl 2 using procedure A.
  • Catalyst 5 is F-D948 supported (l-Me-3-"BuCp) 2 ZrCl 2 metallocene using procedure B.
  • Catalyst 7 is F-D948 supported rac-Me 2 Si(bistetrahydroindenyl)ZrCl 2 using procedure B.
  • Catalyst 8 is F-D948 supported rac-tetramethyldisilylene bis(4-(3',5'-di-tert- butylphenyl)-indenyl) zirconium dichloride using procedure B.
  • Catalyst 9 is F-D948 supported meso-tetramethyldisilylene bis(4-(3',5'-di-tert- butylphenyl)-indenyl) zirconium dichloride using procedure B.
  • Catalyst 10 is D948 supported meso-tetramethyldisilylene bis(4-(3',5'-di-tert- butylphenyl)-indenyl) zirconium dichloride using procedure C.
  • Catalyst 11 is D948 supported rac-tetramethyldisilylene bis(4-(3',5'-di-tert- butylphenyl)-indenyl) zirconium dichloride using procedure C.
  • Catalyst 12 is D948 supported rac/meso (l : l)-tetramethyldisilylene bis(4-(3',5'-di- tert-butylphenyl)-indenyl) zirconium di chloride using procedure C.
  • Catalyst 13 is D948 supported meso-tetramethyldisilylene bis(indenyl) zirconium di chloride using procedure C.
  • Catalyst 14 is D948 supported rac-tetramethyldisilylene bis(indenyl) zirconium di chloride using procedure C.
  • Dilithium 1.1.2.2-tetramethyldisilyl bis(4-( 3 5 '-di-fe -butylphenvD-lH-indenide) A solution of l,2-bis(4-(3,5-di-ter ⁇ -butylphenyl)-lH-inden-l-yl)-l, 1,2,2- tetramethyldisilane (8.13 g, 11.2 mmol) in diethyl ether (100 mL) was precooled to -30°C, then was treated with w BuLi (2.5 M, 9.2 mL, 23.05 mmol). The solution was stirred at room temperature for 2 hrs. All volatiles were evaporated. The residue was washed with pentane (30 mL) and dried under vacuum to give the dilithium compound (8.26, 99%).
  • the solid was reslurried in 80 mL of toluene at 80°C for 30 min and then filtered.
  • the solid was reslurried in 80 mL of toluene at 80°C for 30 min and then filtered a final time.
  • the celstir and solid were washed out with 40 mL of toluene.
  • the solid was then washed with pentane and dried under vacuum for 24 hours. Collected 28.9406 g of a free flowing white powder.
  • meso-tetramethy ldisily lene bis(4-(3 ' ,5 ' -di-tert-butylpheny l)-indeny 1) zirconium dichloride (18.4 mg, 0.0208 mmol) was combined with MAO (0.1726g of a 30% by weight toluene solution) and 2 mL of toluene and stirred for 1 hr.
  • 130°C 948 SMAO 0.5214 g was slurried in 20 mL of toluene and chilled to -35°C The catalyst solution was added to the slurry and the slurry was then stirred for 1 hr. with occasional chilling.
  • the slurry was filtered using a fine glass frit, and then reslurried in 20 mL of toluene and stirred for an additional 30 min at 60°C.
  • the slurry was filtered again, and then reslurried in 20 mL of toluene and stirred for an additional 30 min at 60°C.
  • the slurry was filtered, and then reslurried in 20 mL of toluene and stirred for an additional 30 min at 60°C and then filtered for the final time.
  • the celstir was washed out with 20 mL of toluene and the solid was dried under vacuum. Collected 0.619 g of pink solid.
  • the solid was transferred into a tube furnace, and was heated under constant nitrogen flow (temperature program: 25°C/h ramped to 150°C; held at 150°C for 4 hrs.; 50°C/h ramped to 200°C; held at 200°C for 4 hrs.; cooled down to room temperature). 46 g of F-silica was collected after the calcination. The calculated "F" loading was 0.9 mmol/g.
  • mesotetramethy ldisily lene bis(4-(3 ' ,5 ' -di-tert-butylpheny l)-indeny 1) zirconium dichloride (19.0 mg, 0.0215 mmol) was dissolved in 3 mL of toluene.
  • 600°C 948 SMAO (0.5384 g) was slurried in 15 mL of toluene.
  • the catalyst solution was added to the slurry; the catalyst vial was washed out with another 2 mL of toluene and added to the slurry.
  • the solid is dried under vacuum to give 0.4672 g of yellow solid.
  • the slurry was stirred for 1 hr. before being filtered, washed three times with 15 mL of toluene, and washed twice with pentane. The solid was dried under vacuum to give 1.0013 g of a yellow/orange solid.
  • 600°C 948 SMAO (0.8686 g) was slurried in 15 mL of toluene.
  • Meso- tetramethyldisilylene bis(indenyl) zirconium dichloride (17.5 mg, 0.0345 mmol) was dissolved in 5 mL of toluene and added to the slurry. The slurry was stirred for 1 hr. and then filtered, washed three times with 15 mL of toluene each, and then washed twice with pentane. The solid was dried under vacuum to give 0.7986 g of yellow powder.
  • 600°C 948 SMAO (1.0109 g) was slurried in 15 mL of toluene.
  • Rac- tetramethyldisilylene bis(indenyl) zirconium dichloride (20.4 mg, 0.0403 mmol) was dissolved in 5 mL of toluene and added to the slurry. The slurry was stirred for 1 hr. and then filtered, washed three times with 15 mL of toluene each, and then washed twice with pentane. The solid was dried under vacuum to give 0.9826 g of yellow powder.
  • ethylene homopolymerization and ethylene-hexene copolymerizations are carried out in a parallel pressure reactor, as generally described in US 6306658; US 6455316; WO 00/09255; and Murphy et al, J. Am. Chem. Soc, 2003, Vol. 125, pp. 4306-4317, each of which is incorporated by reference herein in its entirety.
  • specific quantities, temperatures, solvents, reactants, reactants ratios, pressures, and other variables may need to be adjusted from one reaction to the next, the following describes a typical polymerization performed in a parallel, pressure reactor.
  • Solvents, polymerization grade toluene and isohexane are supplied by ExxonMobil Chemical Company and thoroughly dried and degassed prior to use.
  • Polymerization grade ethylene is used and further purified by passing it through a series of columns: 500 cc Oxyclear cylinder from Labclear (Oakland, CA) followed by a 500 cc column packed with dried 3A mole sieves purchased from Aldrich Chemical Company, and a 500 cc column packed with dried 5A mole sieves purchased from Aldrich Chemical Company.
  • TnOAl tri-n-octylaluminum, neat is used as a 2 mmol/L solution in toluene.
  • the autoclaves are prepared by purging with dry nitrogen prior to use.
  • the reactor is prepared as described above, and then purged with ethylene.
  • TnOAl 1-hexene and TnOAl are added via syringe at room temperature and atmospheric pressure.
  • the transition metal compound "TMC" (100 of a 3 mg/mL toluene slurry, unless indicated otherwise) is added via syringe with the reactor at process conditions.
  • TnOAl is used as 200 of a 20 mmol/L in isohexane solution. Amounts of reagents not specified above are given in Table 1. No other reagent is used.
  • Ethylene is allowed to enter (through the use of computer controlled solenoid valves) the autoclaves during polymerization to maintain reactor gauge pressure (+/- 2 psig). Reactor temperature is monitored and typically maintained within +/- 1°C. Polymerizations are halted by addition of approximately 50 psi 02/Ar (5 mol% 02) gas mixture to the autoclaves for approximately 30 seconds. The polymerizations are quenched after a predetermined cumulative amount of ethylene had been added or for a maximum of 45 minutes polymerization time. In addition to the quench time for each run, the reactors are cooled and vented. The polymer is isolated after the solvent is removed in-vacuo. Yields reported include total weight of polymer and residual catalyst. The resultant polymer is analyzed by Rapid GPC to determine the molecular weight and by DSC to determine the melting point.
  • the amount of hexene incorporated in the polymers was determined by rapid FT-IR spectroscopy on a Bruker Vertex 70 IR in reflection mode. Samples were prepared in a thin film format by evaporative deposition techniques. Weight percent hexene was obtained from the ratio of peak heights in the ranges of 1377-1382cm _1 to 4300-4340cm _1 . This method was calibrated using a set of ethylene hexene copolymers with a range of known wt% hexene content.
  • DSC Differential Scanning Calorimetry
  • a 2L autoclave reactor was baked out at 100°C for at least 1 hr.
  • the reactor was cooled to room temperature.
  • 2 mL of a 0.091M TNOAL solution in hexane was loaded into a catalyst tube as a scavenger and injected into the reactor with nitrogen gas.
  • the nitrogen in the reactor was vented down until the pressure was just above ambient pressure.
  • 600 mL of isohexane was added to the reactor.
  • the reactor was heated to 85°C and the stir rate was set to 500 rpm. When the proper temperature had been reached 20 psi of ethylene was added to the reactor.
  • a second cat tube containing the catalyst and 2 mL of pentane was then attached to the reactor.
  • the catalyst was pushed into the reactor with 200 mL of isohexane.
  • a constant ethylene pressure approximately 130 psi on top of the pressure of isohexane, approximately 190 psi total, was bubbled through the cat tube and the reactors dip tube.
  • the reactor stirred for 30 min before being vented and cooled down.
  • the polymer was collected in a beaker and placed under air purge to evaporate the isohexane and collect the dry polymer.
  • a 2L autoclave reactor is baked out at 100°C for at least 1 hr.
  • the reactor is cooled to room temperature.
  • 2 mL of a 0.091M TNOAL solution in hexane is loaded into a catalyst tube as a scavenger and injected into the reactor with nitrogen gas.
  • the nitrogen in the reactor is vented down until the pressure is just above ambient pressure.
  • 300 mL of isohexane is added to the reactor.
  • a second catalyst tube containing 1-hexene is then attached to the reactor.
  • the 1-hexene is injected with an additional 300 mL of isohexane.
  • the reactor is heated to 85°C and the stir rate is set to 500 rpm.
  • RT Room Temperature
  • Mw, Mn and Mw/Mn are determined by using a High Temperature Gel Permeation Chromatography (Agilent PL-220), equipped with three in-line detectors, a differential refractive index detector (DRI), a light scattering (LS) detector, and a viscometer. Experimental details, including detector calibration, are described in: T. Sun, P. Brant, R. R. Chance, and W. W. Graessley, Macromolecules, 2001, Vol. 34(19), pp. 6812-6820, and references therein. Three Agilent PLgel ⁇ Mixed-B LS columns are used. The nominal flow rate is 0.5 mL/min, and the nominal injection volume is 300 ⁇ .
  • the various transfer lines, columns, viscometer and differential refractometer (the DRI detector) are contained in an oven maintained at 145°C.
  • Solvent for the experiment is prepared by dissolving 6 grams of butylated hydroxytoluene as an antioxidant in 4 liters of Aldrich reagent grade 1,2,4- trichlorobenzene (TCB). The TCB mixture is then filtered through a 0.1 ⁇ Teflon filter. The TCB is then degassed with an online degasser before entering the GPC-3D.
  • Polymer solutions are prepared by placing dry polymer in a glass container, adding the desired amount of TCB, then heating the mixture at 160°C with continuous shaking for about 2 hours. All quantities are measured gravimetrically.
  • the TCB densities used to express the polymer concentration in mass/volume units are 1.463 g/mL at room temperature and 1.284 g/mL at 145°C.
  • the injection concentration is from 0.5 to 2.0 mg/mL, with lower concentrations being used for higher molecular weight samples.
  • Prior to running each sample the DRI detector and the viscometer are purged. Flow rate in the apparatus is then increased to 0.5 mL/minute, and the DRI is allowed to stabilize for 8 hours before injecting the first sample.
  • the LS laser is turned on at least 1 to 1.5 hours before running the samples.
  • the concentration, c, at each point in the chromatogram is calculated from the baseline-subtracted DRI signal, 3 ⁇ 4RI, using the following equation:
  • K DRI is a constant determined by calibrating the DRI
  • (dn/dc) is the refractive index increment for the system.
  • concentration is expressed in g/cm 3
  • molecular weight is expressed in g/mole
  • intrinsic viscosity is expressed in dL/g.
  • the LS detector is a Wyatt Technology High Temperature DAWN HELEOS.
  • the molecular weight, M, at each point in the chromatogram is determined by analyzing the LS output using the Zimm model for static light scattering (M.B. Huglin, LIGHT SCATTERING FROM POLYMER SOLUTIONS, Academic Press, 1971):
  • AR(9) is the measured excess Rayleigh scattering intensity at scattering angle ⁇
  • c is the polymer concentration determined from the DRI analysis
  • a 2 is the second virial coefficient
  • ⁇ ( ⁇ ) is the form factor for a monodisperse random coil
  • K 0 is the optical constant for the system:
  • N A is Avogadro's number
  • (dn/dc) is the refractive index increment for the system, which take the same value as the one obtained from DRI method.
  • a high temperature Viscotek Corporation viscometer which has four capillaries arranged in a Wheatstone bridge configuration with two pressure transducers, is used to determine specific viscosity.
  • One transducer measures the total pressure drop across the detector, and the other, positioned between the two sides of the bridge, measures a differential pressure.
  • the specific viscosity, ⁇ 5 for the solution flowing through the viscometer is calculated from their outputs.
  • the intrinsic viscosity, [ ⁇ ] at each point in the chromatogram is calculated from the following equation:
  • ⁇ 5 ⁇ [ ⁇ ] + 0.3( ⁇ [ ⁇ ]) 2
  • the branching index (g' v i s ) 1S calculated using the output of the GPC-DRI-LS-VIS method as follows.
  • ] av g, of the sample is calculated by:
  • Methyl groups per 1000 carbons (CH 3 /1000Carbons) is determined by X H NMR.
  • MI Melt Index
  • High Load Melt Index (HLMI, also referred to as 121) is the melt flow rate measured according to ASTM D-1238 at 190°C, under a load of 21.6 kg.
  • the units for HLMI are g/10 min or dg/min.
  • Melt Index Ratio is the ratio of the high load melt index to the melt index, or 121/12.
  • Catalyst 1 was shown to be the best poor comonomer incorporating catalyst among those tested under similar 1-hexene loading.
  • Catalyst 1 has higher Mw capabilities than another poor comonomer incorporating Catalyst 2 under similar C6 wt% incorporation conditions.
  • Catalyst 8 and Catalyst 9 have higher Mw capabilities than other catalysts under similar 1-hexene feed conditions. As shown in FIG. 4, Catalyst 8 has higher Mw capabilities than another poor comonomer incorporating Catalyst 5 under similar C6 wt% incorporation conditions.
  • Catalyst 10 (meso-tetramethyldisilylene bis(4-(3',5'-di-tert-butylphenyl)-indenyl) ZrC ⁇ ) was compared with Catalyst 13 (meso- Me 4 Si 2 -Ind 2 ZrCl 2 ), in the presence of 1-hexene, Catalyst 10 provided EH copolymers with much lower MI (suggestive of higher Mw) than polymers made with Catalyst 13 under similar conditions.
  • Catalyst 10 (meso-isomer) with 2-H-4-3',5'-di-tert- butylphenyl substitutions on indene fragments has higher Mw capabilities in the presence of comonomer (e.g., 1-hexene) than Catalyst 13 (also meso-isomer) with simple indene fragments. It was noted that in addition to high Mw capabilities, Catalyst 10 has also shown very poor comonomer incorporation capabilities as well as good activities.
  • comonomer e.g., 1-hexene
  • the temperature in the forced convection oven was maintained at 150°C for at least 10 minutes before loading the compression molded samples into the parallel plates.
  • Frequency sweeps in the range of 0.01 to 628 rad/s were carried out at six temperatures: 150°C, 170°C, 190°C, 210°C, 230°C, and 250°C, using strain amplitude of 10%.
  • a stream of nitrogen is circulated in the oven to hinder degradation or crosslinking of the samples during the experiments.
  • Dynamic master curves of the elastic and viscous modulus were constructed using the time-temperature superposition (tTs) principle, that is by horizontally shifting the curves of G' and G" vs. frequency (co), until all the curves overlap.
  • tTs time-temperature superposition
  • the data at 190°C was used as reference for the shifting.
  • ) are computed from the master curve data of G', G" and co, as
  • the linear viscoelastic responses of the six samples show behavior for linear polymers: single monotonic relaxation mode, evidencing absence of long chain branches.
  • compositions, an element or a group of elements are preceded with the transitional phrase “comprising,” it is understood that we also contemplate the same composition or group of elements with transitional phrases “consisting essentially of,” “consisting of,” “selected from the group of consisting of,” or “is” preceding the recitation of the composition, element, or elements and vice versa.

Abstract

La présente invention concerne des composés catalyseurs métallocènes de type bis-indényle d'un nouveau type où le pont est -((R15*)2Si-Si(R15)2)-, chaque R15 et R15* étant identique ou différent et étant un groupe alkyle en C1 à C20 substitué ou non substitué, ramifié ou non ramifié, de préférence chaque R15 ne formant pas ensemble un cycle, et/ou chaque R15* ne formant pas ensemble un cycle, et/ou R15 et R15* ne formant pas ensemble un cycle. La présente invention concerne également des procédés de polymérisation pour produire un polymère et des compositions polymères produites par les procédés décrits.
PCT/US2016/033583 2015-07-15 2016-05-20 Composés catalyseurs métallocènes de type bis-indényle substitué comprenant un pont -si-si- WO2017011073A1 (fr)

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EP16824842.5A EP3322529A4 (fr) 2015-07-15 2016-05-20 Composés catalyseurs métallocènes de type bis-indényle substitué comprenant un pont -si-si-
BR112018000843A BR112018000843A2 (pt) 2015-07-15 2016-05-20 compostos catalisadores de bis indenil metaloceno substituído que compreendem ponte de -si-si-
CN201680041437.7A CN107847920A (zh) 2015-07-15 2016-05-20 包含‑Si‑Si‑桥基的取代的双茚基茂金属催化剂化合物

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US10851187B2 (en) 2018-01-31 2020-12-01 Exxonmobil Chemical Patents Inc. Bridged metallocene catalysts with a pendant group 13 element, catalyst systems containing same, processes for making a polymer product using same, and products made from same
US10865258B2 (en) 2018-01-31 2020-12-15 Exxonmobil Chemical Patents Inc. Mixed catalyst systems containing bridged metallocenes with a pendant group 13 element, processes for making a polymer product using same, and products made from same
US11130827B2 (en) 2017-11-14 2021-09-28 Exxonmobil Chemical Patents Inc. Polyethylene compositions and articles made therefrom

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CN110041529B (zh) * 2019-04-04 2021-06-22 天津大学 一种丁烯接枝聚乙二醇共聚物及其制备方法
JP2023513582A (ja) * 2020-02-11 2023-03-31 エクソンモービル ケミカル パテンツ インコーポレイテッド 遷移金属ビス（フェノラート）触媒錯体を用いて得られるエチレン－アルファオレフィン－ジエンモノマーのコポリマー及びその生成のための均一プロセス

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US11130827B2 (en) 2017-11-14 2021-09-28 Exxonmobil Chemical Patents Inc. Polyethylene compositions and articles made therefrom
US10851187B2 (en) 2018-01-31 2020-12-01 Exxonmobil Chemical Patents Inc. Bridged metallocene catalysts with a pendant group 13 element, catalyst systems containing same, processes for making a polymer product using same, and products made from same
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