EP2794688A1 - Systèmes de catalyseur de métallocène multi-composants pour la fabrication de mélanges en réacteur de polypropylène - Google Patents

Systèmes de catalyseur de métallocène multi-composants pour la fabrication de mélanges en réacteur de polypropylène

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Publication number
EP2794688A1
EP2794688A1 EP12877323.1A EP12877323A EP2794688A1 EP 2794688 A1 EP2794688 A1 EP 2794688A1 EP 12877323 A EP12877323 A EP 12877323A EP 2794688 A1 EP2794688 A1 EP 2794688A1
Authority
EP
European Patent Office
Prior art keywords
catalyst
catalyst component
indenyl
dimethylsilylbis
zirconiuma
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP12877323.1A
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German (de)
English (en)
Other versions
EP2794688A4 (fr
Inventor
David J. Rauscher
Jun Tian
William J. Gauthier
Shady N. Henry
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Fina Technology Inc
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Fina Technology Inc
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Publication date
Priority claimed from US13/476,145 external-priority patent/US20120322961A1/en
Application filed by Fina Technology Inc filed Critical Fina Technology Inc
Publication of EP2794688A1 publication Critical patent/EP2794688A1/fr
Publication of EP2794688A4 publication Critical patent/EP2794688A4/fr
Withdrawn legal-status Critical Current

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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
    • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • 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
    • C08F210/04—Monomers containing three or four carbon atoms
    • C08F210/06—Propene
    • 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
    • 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
    • C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
    • C08F4/65922—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not
    • C08F4/65927—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not two cyclopentadienyl rings being mutually bridged

Definitions

  • Embodiments of the present invention generally relate to processes and catalyst systems for forming polyolefins.
  • embodiments relate to multicomponent metallocene catalyst systems for forming blends of polypropylene in-situ.
  • embodiments relate to multicomponent metallocene catalyst systems for forming reactor blends of polypropylene or random copolymers of propylene with broadening of molecular weight distribution. Additionally, the catalyst activity may be enhanced.
  • Metallocene compounds can further be characterized in terms of stereoregular catalysts which can facilitate the polymerization of alpha olefins, such as propylene, to produce crystalline stereoregular polymers, the most common of which are isotactic polypropylene and syndiotactic polypropylene.
  • stereospecific metallocene catalysts possess a center structure and one or more ligand structures (usually cyclopentadienyl-based) that are conformationally restricted.
  • the center structure of stereospecific metallocene catalysts is typically chiral in conformation.
  • a chiral object is not superimposible on its mirror image, examples of chiral objects include hands and keys.
  • Isospecific and syndiospecific metallocene catalysts can be useful in the stereospecific polymerization of monomers.
  • Stereospecific structural relationships of syndiotacticity and isotacticity may be involved in the formation of stereoregular polymers from various monomers.
  • Stereospecific propagation may be applied in the polymerization of ethylenically unsaturated monomers such as C 3 to C 20 alpha olefins which can be linear, branched, or cyclic, 1-dienes such as 1,3-butadiene, substituted vinyl compounds such as vinyl aromatics, e.g., styrene or vinyl chloride, vinyl chloride, vinyl ethers such as alkyl vinyl ethers, e.g., isobutyl vinyl ether, or even aryl vinyl ethers.
  • ethylenically unsaturated monomers such as C 3 to C 20 alpha olefins which can be linear, branched, or cyclic, 1-dienes such as 1,3-butadiene, substituted vinyl compounds such as vinyl aromatics, e.g., styrene or vinyl chloride, vinyl chloride, vinyl ethers such as alkyl vinyl ethers, e.g., isobutyl vinyl ether, or
  • isotactic polypropylene can be described as one having the methyl groups attached to the tertiary carbon atoms of successive monomelic units falling on the same side of a hypothetical plane through the main chain of the polymer, e.g., the methyl groups are all above or below the plane.
  • the stereochemical sequence of isotactic polypropylene can be described as follows:
  • each vertical segment indicates a methyl group on the same side of the polymer backbone.
  • isotactic polypropylene the majority of inserted propylene units possess the same relative configuration in relation to its neighboring propylene unit.
  • Another way of describing the structure is through the use of NMR. Bovey's MR nomenclature for an isotactic sequence as shown above is ...mmmm... with each "m” representing a "meso" dyad in which there is a mirror plane of symmetry between two adjacent monomer units, or successive pairs of methyl groups on the same side of the plane of the polymer chain. As is known in the art, any deviation or inversion in the structure of the chain lowers the degree of isotacticity and subsequently the crystallinity of the polymer.
  • syndiotactic propylene polymers are those in which the methyl groups attached to the tertiary carbon atoms of successive monomeric units in the chain lie on alternate sides of the plane of the polymer.
  • Syndiotactic polypropylene in using the Fischer projection formula can be indicated by racemic dyads with the syndiotactic sequence ....rrrr.... shown as follows:
  • Bovey's NMR nomenclature for a syndiotactic sequence as shown above is ...rrrr... with each V representing a "racemic" dyad in which successive pairs of methyl groups are on the opposite sides of the plane of the polymer chain. Similarly, any deviation or inversion in the structure of the chain lowers the degree of syndiotacticity and subsequently the crystallinity of the polymer.
  • the vertical segments in the preceding example indicate methyl groups in the case of syndiotactic or isotactic polypropylene.
  • Other terminal groups e.g. ethyl, in the case of polyl- butene, chloride, in the case of polyvinyl chloride, or phenyl groups in the case of polystyrene and so on can be equally described in this fashion as either isotactic or syndiotactic.
  • a polymer is "atactic" when its pendant groups are arranged in a random fashion on both sides of the chain of the polymer.
  • Reducing per pound resin manufacturing cost for the production of metallocene polypropylene may be achieved through increasing catalyst activity.
  • Narrow molecular weight distribution of miPP metallocene random copolymers can result in resins that are tough to process (high power input, shark skin and melt fracture, etc.).
  • Embodiments of the invention generally include multicomponent catalyst systems.
  • the multicomponent catalyst system generally includes a first catalyst component selected from a metallocene catalyst represented by the general formula XCp A Cp B MA n , wherein X is a structural bridge, Cp A and Cp B each denote a cyclopentadienyl group or derivatives thereof, each being the same or different and which may be either substituted or unsubstituted, M is a transition metal and A is an alkyl, hydrocarbyl or halogen group and n is an integer between 0 and 4.
  • a metallocene catalyst represented by the general formula XCp A Cp B MA n , wherein X is a structural bridge, Cp A and Cp B each denote a cyclopentadienyl group or derivatives thereof, each being the same or different and which may be either substituted or unsubstituted, M is a transition metal and A is an alkyl, hydrocarbyl or
  • the multicomponent catalyst system further includes a second catalyst component generally represented by the formula XCp A Cp B MA n , wherein X is a structural bridge, Cp A and Cp B each denote a cyclopentadienyl group or derivatives thereof, each being the same or different and which may be either substituted or unsubstituted, M is a transition metal and A is an alkyl, hydrocarbyl or halogen group and n is an integer between 0 and 4.
  • the first and second catalyst components are different.
  • One embodiment includes a process further including introducing the multicomponent metallocene catalyst system to a reaction zone, introducing an olefin monomer to the reaction zone and contacting the multicomponent catalyst system with the olefin monomer to form a polyolefin.
  • Embodiments further include the introduction of a second olefin monomer into a reaction zone, resulting in a random copolymer.
  • Figure 1 illustrates the effect of 'n' metallocene content in the supported catalysts on the polymerization activity and fluff bulk density (2.0 wt% in total).
  • Figure 2 illustrates the effect of 'm' metallocene content in the supported catalysts on the fluff melt flow.
  • Figure 5 illustrates the propylene polymerization activities of MAO/P10 supported catalysts with different metallocene mixing ratio (loading 2.0 wt%) under different initial hydrogen concentrations.
  • Figure 6 illustrates the melt flow of polypropylene fluffs from MAO/P10 supported catalysts with different metallocene mixing ratios (loading 2.0 wt%) under different initial hydrogen concentration.
  • Figure 7 illustrates the bulk density of polypropylene fluffs from MAO/P10 supported catalyst with different metallocene mixing ratios (loading 2.0 wt%) under different initial hydrogen concentation.
  • Figure 8 is a gel permeation chromatograph of polypropylene resin from 'm + n' catalysts with different mixing ratio.
  • Figure 9 illustrates the polydispersity of polypropylene resins from MAO/PIO supported catalysts with different metallocene mixing ratios but the same loading (2.0 wt%) under different initial hydrogen concentration.
  • Figure 11 is a gel permeation chromatograph of polypropylene resins from 'm + n'
  • Figure 12 a gel permeation chromatograph of polypropylene resins from 'm + n'
  • Figure 13 illustrates the melt flow of polymer fluffs from both 'm + n' and 'm' + 'n' MAO/P10 supported catalysts with different ( m': ( n' ratios.
  • Figure 14 illustrates the molecular weight distribution of polymer fluffs from both 'm
  • Figure 15 is a comparison of ethylene copolymerization behavior of miPP catalysts.
  • Figure 16 is a comparison of ethylene incorporation rates for m, n, and AR35 catalysts.
  • Figure 17 is a comparison of crystallinity as a function of peak melting temperature
  • Figure 18 illustrates the relationship between xylene soluble and copolymer melting temperature.
  • the term "activity" refers to the weight of product produced per weight of the catalyst used in a process at a standard set of conditions per unit time.
  • activator is defined to be any compound or combination of compounds, supported or unsupported, which may enhance the activity and/or productivity of a catalyst compound.
  • C 6 rtain polymerization processes disclosed herein involve contacting olefin monomers with a multicomponent metallocene catalyst composition, sometimes also referred to herein as simply a multicomponent catalyst.
  • a multicomponent metallocene catalyst composition sometimes also referred to herein as simply a multicomponent catalyst.
  • multicomponent catalyst composition and “multicomponent catalyst” refer to any composition, mixture or system that includes at least two different catalyst compounds. Although it is contemplated that the multicomponent catalyst can include more than two different catalysts, for purposes of discussing the invention herein, only two of those catalyst compounds are described in detail herein (i.e., the "first catalyst component” and the "second catalyst component”).
  • the multicomponent catalyst compositions described herein include a "first catalyst component".
  • the first catalyst component generally includes catalyst systems known to one skilled in the art.
  • the first catalyst component may include metallocene catalyst systems, single site catalyst systems, or combinations thereof, for example.
  • a brief discussion of such catalyst systems is included below, but is in no way intended to limit the scope of the invention to such catalysts.
  • Metallocene catalysts may be characterized generally as coordination compounds incorporating one or more cyclopentadienyl (Cp) groups (which may be substituted or unsubstituted, each substitution being the same or different) coordinated with a transition metal through ⁇ bonding.
  • Cp cyclopentadienyl
  • the substituent groups on Cp may be linear, branched or cyclic hydrocarbyl radicals, for example.
  • the inclusion of cyclic hydrocarbyl radicals may transform the Cp into other contiguous ring structures, such as indenyl, azulenyl and fluorenyl groups, for example.
  • These contiguous ring structures may also be substituted or unsubstituted by hydrocarbyl radicals, such as C 1 to CM hydrocarbyl radicals, for example.
  • a specific, non-limiting, example of a metallocene catalyst is a bulky ligand metallocene compound generally represented by the formula:
  • L is a bulky ligand
  • A is a leaving group
  • M is a transition metal
  • m and n are such that the total ligand valency corresponds to the transition metal valency.
  • m may be from 1 to 4 and n may be from 1 to 3.
  • the metal atom "M" of the metallocene catalyst compound may be selected from Groups 3 through 12 atoms and lanthanide Group atoms, or from Groups 3 through 10 atoms or from Sc, Ti, Zr, Hf, V, Nb, Ta, Mn, Re, Fe, Ru, Os, Co, Rh, Ir and Ni.
  • the oxidation state of the metal atom "M” may range from 0 to +7 or is +1, +2, +3, +4 or +5, for example.
  • the bulky ligand generally includes a cyclopentadienyl group (Cp) or a derivative thereof.
  • the Cp ligand(s) form at least one chemical bond with the metal atom M to form the "metallocene catalyst.”
  • the Cp ligands are distinct from the leaving groups bound to the catalyst compound in that they are not highly susceptible to substitution/abstraction reactions.
  • Cp ligands may include ring(s) or ring system(s) including atoms selected from group 13 to 16 atoms, such as carbon, nitrogen, oxygen, silicon, sulfur, phosphorous, germanium, boron, aluminum and combinations thereof, wherein carbon makes up at least 50% of the ring members.
  • Non-limiting examples of the ring or ring systems include cyclopentadienyl, cyclopentaphenanthreneyl, indenyl, benzindenyl, fluorenyl, tetrahydroindenyl, octahydrofluorenyl, cyclooctatetraenyl, cyclopentacyclododecene, phenanthrindenyl, 3,4- benzofluorenyl, 9-phenylfluorenyl, 8-H-cyclopent[a]acenaphthylenyl, 7-H-dibenzofluorenyl, indeno[1,2-9]anthrene, thiophenoindenyl, thiophenofluorenyl, hydrogenated versions thereof (e.g., 4,5,6,7-tetrahydroindenyl or "H 4 Ind”), substituted versions thereof and heterocyclic versions thereof, for example.
  • Cp substituent groups may include hydrogen radicals, alkyls (eg., methyl, ethyl, propyl, butyl, pentyl, hexyl, fluoromethyl, fluoroethyl, difluoroethyl, iodopropyl, bromohexyl, benzyl, phenyl, methylphenyl, tert-butylphenyl, chlorobenzyl, dimethylphosphine and methylphenylphosphine), alkenyls (e.g., 3-butenyl, 2-propenyl and S-hexenyl), alkynyls, cycloalkyls (e.g., cyclopentyl and cyclohexyl), aryls (e.g., trimethylsilyl, trimethylgermyl, methyldiethylsilyl, acyls, aroyls, tris(trifluorfluor
  • Each leaving group "A" is independently selected and may include any ionic leaving group, such as halogens (e.g., chloride and fluoride), hydrides, C 1 to C 12 alkyls (e.g., methyl, ethyl, propyl, phenyl, cyclobutyl, cyclohexyl, heptyl, tolyl, trifluoromethyl, methylphenyl, dimethylphenyl and trimethylphenyl), C 2 to C 12 alkenyls (e.g., C 2 to C 6 fluoroalkenyls), C 6 to C 12 aryls (e.g., C 7 to C 20 alkylaryls), C 1 to C 12 alkoxys (e.g., phenoxy, methyoxy, ethyoxy, propoxy and benzoxy), C 6 to C
  • leaving groups include amines, phosphines, ethers, carboxylates (e.g., C 1 to C 6 alkylcarboxylates, C 6 to C 12 arylcarboxylates and C 7 to C 18 alkylarylcarboxylates), dienes, alkenes (e.g., tetramethylene, pentamethylene, methylidene), hydrocarbon radicals having from 1 to 20 carbon atoms (e.g., pentafluorophenyl) and combinations thereof, for example.
  • two or more leaving groups form a part of a fused ring or ring system.
  • L and A may be bridged to one another to form a bridged metallocene catalyst.
  • a bridged metallocene catalyst for example, may be described by the general formula: wherein X is a structural bridge, Cp A and Cp B each denote a cyclopentadienyl group or derivatives thereof, each being the same or different and which may be either substituted or unsubstituted, M is a transition metal and A is an alkyl, hydrocarbyl or halogen group and n is an integer between 0 and 4, and either 1 or 2 in a particular embodiment.
  • Non-limiting examples of bridging groups "X" include divalent hydrocarbon groups containing at least one Group 13 to 16 atom, such as, but not limited to, at least one of a carbon, oxygen, nitrogen, silicon, aluminum, boron, germanium, tin and combinations thereof; wherein the heteroatom may also be a C 1 to C 12 alkyl or aryl group substituted to satisfy a neutral valency.
  • the bridging group may also contain substituent groups as defined above including halogen radicals and iron.
  • the bridged metallocene catalyst component has two or more bridging groups.
  • bridging groups include methylene, ethylene, ethylidene, propylidene, isopropylidene, diphenylmethylene, 1,2-dimethylethylene, 1,2- diphenylethylene, 1,1,2,2-tetramethylethylene, dimethylsilyl, diethylsilyl, methyl-ethylsilyl, trifluoromethylbutylsilyl, bis(trifluoromethyl)silyl, di(n-butyl)silyl, di(n-propyl)silyl, di(i- propyl)silyl, di(n-hexyl)silyl, dicyclohexylsilyl, diphenylsilyl, cyclohexylphenylsilyl, t- butylcyclohexylsilyl, di(t-butylphenyl)silyl, di(p-tolyl)silyl and the corresponding moie
  • the bridging group may also be cyclic and include 4 to 10 ring members or 5 to 7 ring members, for example.
  • the ring members may be selected from the elements mentioned above and/or from one or more of boron, carbon, silicon, germanium, nitrogen and oxygen, for example.
  • Non-limiting examples of ring structures which may be present as or part of the bridging moiety are cyclobutylidene, cyclopentylidene, cyclohexylidene, cycloheptylidene, cyclooctylidene, for example.
  • the cyclic bridging groups may be saturated or unsaturated and/or carry one or more substituents and/or be fused to one or more other ring structures.
  • the one or more Cp groups which the above cyclic bridging moieties may optionally be fused to may be saturated or unsaturated. Moreover, these ring structures may themselves be fused, such as, for example, in the case of a naphthyl group.
  • the metallocene catalyst includes CpFlu Type catalysts (e.g., a metallocene catalyst wherein the ligand includes a Cp fluorenyl ligand structure) represented by the following formula:
  • Cp is a cyclopentadienyl group or derivatives thereof
  • Fl is a fluorenyl group
  • X is a structural bridge between Cp and Fl
  • R is an optional substituent on the Cp
  • n is 1 or 2
  • R 2 is an optional substituent on the Cp bound to a carbon immediately adjacent to the ipso carbon
  • m is 1 or 2
  • each R 3 is optional, may be the same or different and may be selected from CI to C 2 0 hydrocarbyls.
  • at least one R 3 is substituted in the para position on the fluorenyl group and at least one other R 3 being substituted at an opposed para position on the fluorenyl group and p is 2 or 4.
  • the metallocene catalyst includes bridged mono-ligand metallocene compounds (e.g., mono cyclopentadienyl catalyst components).
  • the metallocene catalyst is a bridged "half-sandwich” metallocene catalyst.
  • the at least one metallocene catalyst component is an unbridged "half sandwich” metallocene.
  • Non-limiting examples of metallocene catalyst components consistent with the description herein include, for example cyclopentadienylzirconiumA n ; indenylzirconiumA n ; (1- methylindenyl)zirconiumA n ; (2-methylindenyl)zirconiumA n , (l-propylindenyl)zirconiumA n ; (2- propylindenyl)zirconiumA n ; (1 -butylindenyl)zirconiumA n ; (2-butylindenyl)zirconiumA n ; methylcyclopentadienylzirconiumAn; tetrahydroindenylzirconiumA n pentamethylcyclopentadienylzirconiumA n ; cyclopentadienylzirconiumAn; pentamethylcyclopentadienylzirconiumA n ;
  • dimethylsilylcyclopentadienylindenylzirconiumA n dimethylsilyl(2- methylindenyl)(fluorenyl)zirconiumA endeavor; diphenylsilyl(1,2,3,4-tetramethylcyclopentadienyl)(3- propylcyclopentadienyl)zirconiumA n ; dimethylsilyl (1,2,3,4-tetramethylcyclopentadienyl) (3-t- butylcyclopentadienyl)zirconiumAn; dimethylgermyl(1,2-dimethylcyclopentadienyl)(3- isopropylcyclopentadienyl)zirconiumA n ; dimethylsilyl(1,2,3,4-tetramethylcyclopentadienyl)(3- methylcyclopentadienyl)zirconiumA n ; diphenylmethylidene(cyclopentt
  • dimethylsilylbis(trimethylsilylcyclopentadienyl)zirconiumA n ; dimethylsilylbis(2-trimethylsilyl- 4-t-butylcyclopentadienyl)zirconiumA n ; dimethylsilylbis(4,5,6,7-tetrahydro- indenyl)zirconiumA incident; dimethylsilylbis(indenyl)zirconiumAn; dimethylsilylbis(2- methylindenyl)zirconiumA n ; dimethylsilylbis(2 > 4-dimethylindenyl)zirconiumA n ; dimethylsilylbis(2,4,7-trimethyIindenyl)zirconiumA represents; dimethylsilylbis(2-methyl-4- phenylindenyl)zirconiumA n ; dimethylsilylbis(2-ethyl-4-phenylindenyl)zirconiumA n ;
  • the first catalyst component includes a metallocene catalyst, such as dimethylsilylbis(2-me l-4-phenyl-indenyl)zirconium dichloride, dimethyIsilylbis(2-methyl-indenyl)zirconium dichloride, dimethylsilylbis(2-methyl-4,5-benzo- indenyl)zirconium dichloride, for example.
  • the first catalyst component comprises dimethylsilylbis(2-methyl-4-phenyl-indenyl)zirconium dichloride, for example.
  • the first catalyst component includes a metallocene catalyst capable of producing a polymer having a high melting point (e.g. t a T m of from about 135°C to about 165°C or from about 140°C to about 160°C or from 145°C to about 155°C).
  • a metallocene catalyst capable of producing a polymer having a high melting point (e.g. t a T m of from about 135°C to about 165°C or from about 140°C to about 160°C or from 145°C to about 155°C).
  • the multicomponent catalyst compositions include a "second catalyst component".
  • the second catalyst component generally includes a metallocene catalyst as described above.
  • the second catalyst component includes a metallocene catalyst, such as dimethylsiIylbis(2-methyl-4-phenyl-indenyl)zirconium dichloride, dimethylsilylbis(2-methyl-indenyl)zirconium dichloride, dimethylsilylbis(2-methyl-4,5-benzo- indenyl)zirconium dichloride, for example.
  • the first catalyst component comprises dimethylsilylbis(2-methyl-indenyl)zirconium dichloride, for example.
  • the second catalyst component is different from the first catalyst component.
  • the multicomponent catalyst system may have a ratio of first catalyst component to second catalyst component of from 1.5:1.0 or from 1.0:1.5 on a weight basis. Metallocene loading ranges from 1.0 to 2.5 wt% or from 1.5 to 2.0 wt%.
  • the first catalyst component may be present in the multicomponent catalyst system in an amount as much as 70 wt% of the total catalyst system, or as much as 67 wt%, or as much as 60 wt%.
  • the methods described herein further include contacting one or more of the catalyst components with a catalyst activator, herein simply referred to as an "activator".
  • the activator may include a single composition capable of activating both the first catalyst component and the second catalyst component.
  • the metallocene catalysts may be activated with a metallocene activator for subsequent polymerization.
  • a metallocene activator for subsequent polymerization.
  • the term "metallocene activator 11 is defined to be any compound or combination of compounds, supported or unsupported, which may activate a single-site catalyst compound (e.g. t metallocenes, Group 15 containing catalysts, etc.) This may involve the abstraction of at least one leaving group (A group in the formulas/structures above, for example) from the metal center of the catalyst component.
  • the metallocene catalysts are thus activated towards olefin polymerization using such activators.
  • Embodiments of such activators include Lewis acids, such as cyclic or oligomeric polyhydrocarbylaluminum oxides, non-coordinating ionic activators ("NCA"), ionizing activators, stoichiometric activators, combinations thereof or any other compound that may convert a neutral metallocene catalyst component to a metallocene cation that is active with respect to olefin polymerization.
  • the Lewis acids may include alumoxane (e.g., "MAO”), modified alumoxane ⁇ e.g., "TIBAO”) and alkylaluminum compounds, for example.
  • Non-limiting examples of aluminum alkyl compounds may include trimethylaluminum, triethylaluminum, triisobutylaluminum, tri-n- hexylaluminum and tri-n-octylaluminum, for example.
  • Ionizing activators are well known in the art and are described by, for example, Eugene You-Xtan Chen & Tobin J. Marks, Cocatalysts for Metal-Catalyzed Olefin Polymerization: Activators, Activation Processes, and Structure-Activity Relationships 100(4) CHEMICAL REVIEWS 1391-1434 (2000).
  • neutral ionizing activators include Group 13 tri-substituted compounds, in particular, tri-substituted boron, tellurium, aluminum, gallium and indium compounds and mixtures thereof (e.g., tri(n-butyl)ammonium- tetrakis(pentafluorophenyl)borate and/or trisperfiuorophenyl boron metalloid precursors), for example.
  • the substituent groups may be independently selected from alkyls, alkenyls, halogen, substituted alkyls, aryls, arylhalides, alkoxy and halides, for example.
  • the three groups are independently selected from halogens, mono or multicyclic (including halosubstituted) aryls, alkyls, alkenyl compounds and mixtures thereof, for example.
  • the three groups are selected from C 1 to C1 ⁇ 4o alkenyls, C 1 to C 2 0 alkyls, C 1 to C 2 0 alkoxys, C3 to ⁇ 1 ⁇ 4o aryls and combinations thereof, for example.
  • the three groups are selected from the group highly halogenated C 1 to Q alkyls, highly halogenated phenyls, and highly halogenated naphthyls and mixtures thereof, for example.
  • highly halogenated it is meant that at least 50% of the hydrogens are replaced by a halogen group selected from fluorine, chlorine and bromine.
  • Illustrative, not limiting examples of ionic ionizing activators include trialkyl- substituted ammonium salts (e.g., triethylammoniumtetraphenylborate, tripropylammoniumtetraphenylborate, tri(n-butyl)anunoniumtetraphenylborate, trimethylammoniumtetra(p-tolyl)borate, trimethylammoniumtetra(o-tolyl)borate, tributylammoniumtetra(pentafluorophenyl)borate, tripropylammoniumtetra(o,p- dimethylphenyl)borate, tributylarmnoniumtetra(m,m-dimethylphenyl)borate, tributylammoniumtetra(p-tri-fluoromethylphenyl)borate,
  • trialkyl- substituted ammonium salts e.g., triethyl
  • N,N-dialkylanilinium salts e.g., ⁇ , ⁇ -dimethylaniliniumtetraphenylborate, N,N- diethylaniliniumtetraphenylborate and N,N-2,4,6-pentamethylaniliniumtetraphenylborate
  • dialkyl ammonium salts e.g., diisopropylammoniumtetrapentafluorophenylborate and dicyclohexylammoniumtetraphenylborate
  • triaryl phosphonium salts e.g. t triphenylphosphoniumtetraphenylborate, trimethylphenylphosphoniumtetraphenylborate and tridimethylphenylphosphoniumtetraphenyl
  • an alkylaluminum compound may be used in conjunction with a heterocyclic compound.
  • the ring of the heterocyclic compound may include at least one nitrogen, oxygen, and/or sulfur atom, and includes at least one nitrogen atom in one embodiment.
  • the heterocyclic compound includes 4 or more ring members in one embodiment, and 5 or more ring members in another embodiment, for example.
  • the heterocyclic compound for use as an activator with an alkylaluminum compound may be unsubstituted or substituted with one or a combination of substituent groups.
  • suitable substituents include halogens, alkyls, alkenyls or alkynyl radicals, cycloalkyl radicals, aryl radicals, aryl substituted alkyl radicals, acyl radicals, aroyl radicals, alkoxy radicals, aryloxy radicals, alkylthio radicals, dialkylamino radicals, alkoxycarbonyl radicals, aryloxycarbonyl radicals, carbomoyl radicals, alkyl- or dialkyl- carbamoyl radicals, acyloxy radicals, acylamino radicals, aroylamino radicals, straight, branched or cyclic, alkylene radicals or any combination thereof, for example.
  • Non-limiting examples of hydrocarbon substituents include methyl, ethyl, propyl, butyl, pentyl, hexyl, cyclopentyl, cyclohexyl, benzyl, phenyl, fluoromethyl, fluoroethyl, difluoroethyl, iodopropyl, bromohexyl or chlorobenzyl, for example.
  • Non-limiting examples of heterocyclic compounds utilized include substituted and unsubstituted pyrroles, imidazoles, pyrazoles, pyrrolines, pyrrolidines, purines, carbazoles, indoles, phenyl indoles, 2,5-dimethylpyrroles, 3-pentafluorophenylpyrrole, 4,5,6,7- tetrafluoroindole or 3,4-difluoropyrroles, for example.
  • activators are also contemplated by the invention, for example, alumoxanes and ionizing activators in combinations.
  • Other activators include aluminum boron complexes, perchlorates, periodates and iodates including their hydrates, lithium (2,2-bisphenyl- ditrimethylsilicate)-4T- HF and silylium salts in combination with a non-coordinating compatible anion, for example.
  • methods of activation such as using radiation and electro-chemical oxidation are also contemplated as activating methods for the purposes of enhancing the activity and/or productivity of a single-site catalyst compound, for example. (See, U.S. Pat. No. 5,849,852, U.S. Pat. No. 5,859,653, U.S. Pat. No. 5,869,723 and WO 98/32775.)
  • the catalyst may be activated in any manner known to one skilled in the art.
  • the catalyst and activator may be combined in molar ratios of activator to catalyst of from 1000:1 to 0.1:1, or from 500:1 to 1:1, or from about 100:1 to about 250:1, or from 150:1 to 1:1, or from 50:1 to 1:1, or from 10:1 to 0.5:1 or from 3:1 to 0.3:1, for example.
  • the activators may or may not be associated with or bound to a support, either in association with one or more catalyst component or separate from the catalyst component(s), such as described by Gregory G. Hlatky, Heterogeneous Single-Site Catalysts for Olefin Polymerization 100(4) CHEMICAL REVIEWS 1347-1374 (2000).
  • each different catalyst component may reside on a single support particle, so that the multicomponent catalyst is a supported multicomponent catalyst.
  • the term multicomponent catalyst also broadly includes a system or mixture in which one of the catalysts (e.g., the first catalyst component) resides on one collection of support particles and another catalyst (e.g., the second catalyst component) resides on another collection of support particles.
  • the two supported catalysts are introduced to a single reactor, either simultaneously or sequentially and polymerization is conducted in the presence of the multicomponent catalyst.
  • an unsupported version of the multicomponent catalyst described herein can be used in a polymerization process, i.e., in which the monomers are contacted with a multicomponent catalyst that is not supported.
  • the support materials may include talc, inorganic oxides, clays and clay minerals, ion-exchanged layered compounds, diatomaceous earth compounds, zeolites or a resinous support material, such as a polyolefin, for example.
  • silica supports include P10 (available from Fuji-Silysia).
  • the silica is modified with MAO (methylaluminoxane).
  • Specific inorganic oxides include silica, alumina, magnesia, titania and zirconia, for example.
  • the inorganic oxides used as support materials may have an average particle size of from 5 microns to 600 microns or from 10 microns to 100 microns, a surface area of from 50 m 2 /g to 1,000 m 2 /g or from 100 m 2 /g to 400 m 2 /g and a pore volume of from 0.5cc/g to 3.5 cc/g or from 0.5 cc g to 2 cc/g, for example.
  • Methods for supporting metallocene catalysts are generally known in the art. (See, U.S. Patent No. 5,643,847, U.S. Patent No. 09184358 and 09184389, which are incorporated by reference herein.)
  • one procedure for preparing a supported multicomponent catalyst can include providing a supported first catalyst component, contacting a slurry including the first catalyst component and a non-polar hydrocarbon with a mixture (solution or slurry) that includes the second catalyst component, which may also include an activator. The procedure may further include drying the resulting product that includes the first and second catalyst components and recovering a multicomponent catalyst composition.
  • Another method may include reacting the silica (such as P10) with MAO in a hydrocarbon solvent and heat to form an MAO-modified silica.
  • Subsequent steps then include adding the first catalyst component to the MAO-modified silica, then adding the second catalyst component to form a multicomponent catalyst on a single support.
  • Another method may include mixing the first catalyst component and the second catalyst component in a solvent then adding the MAO-modified silica.
  • Another method may include supporting the first catalyst component on a first MAO-modified silica and supporting the second catalyst component on a second MAO-modified silica and physically mixing the supported catalysts.
  • the first and second catalyst components may be independently fed to one or more reaction zones, so long as each reaction zone includes a multicomponent system as described herein.
  • Resin reactor blending can be achieved by either separate supported catalysts mixing inside the catalyst pot before being injected into the loop reactor (Metallocene Catalyst Mixing) or metallocene deposition on the same support during the supported catalyst preparation (Metallocene Catalyst Co-Supporting).
  • the support material, one or more of the catalyst components, the catalyst system or combinations thereof may be contacted with one or more scavenging compounds prior to or during polymerization.
  • scavenging compounds is meant to include those compounds effective for removing impurities (e.g., polar impurities) from the subsequent polymerization reaction environment. Impurities may be inadvertently introduced with any of the polymerization reaction components, particularly with solvent, monomer and catalyst feed, and adversely affect catalyst activity and stability. Such impurities may result in decreasing, or even elimination, of catalytic activity, for example.
  • the polar impurities or catalyst poisons may include water, oxygen and metal impurities, for example.
  • the scavenging compound may include an excess of the aluminum containing compounds described above, or may be additional known organometallic compounds, such as Group 13 organometallic compounds.
  • the scavenging compounds may include trimethyl aluminum (TMA), triisobutyl aluminum ( ⁇ 1), methylalumoxane (MAO), isobutyl aluminoxane, triethylaluminum (TEAl), and tri-n-octyl aluminum.
  • TMA trimethyl aluminum
  • MAO methylalumoxane
  • TEAl triethylaluminum
  • the scavenging compound is TIBA1.
  • the amount of scavenging compound is minimized during polymerization to that amount effective to enhance activity and avoided altogether if the feeds and polymerization medium may be sufficiently free of impurities.
  • the processes described above generally include polymerizing one or more olefin monomers to form polymers.
  • the olefin monomers may include (1 ⁇ 4 to Cjo olefin monomers, or ⁇ 1 ⁇ 4 to Cu olefin monomers (e.&, ethylene, propylene, butene, pentene, methylpentene, hexene, octene and decene), for example.
  • Other monomers include ethylenically unsaturated monomers, Gj to CM diolefins, conjugated or nonconjugated dienes, polyenes, vinyl monomers and cyclic olefins, for example.
  • Non-limiting examples of other monomers may include norbornene, nobornadiene, isobutylene, isoprene, vinylbenzocyclobutane, sytrene, alkyl substituted styrene, ethylidene norbornene, dicyclopentadiene and cyclopentene, for example.
  • the formed polymer may include homopolymers, copolymers or terpolymers, for example.
  • One example of a gas phase polymerization process includes a continuous cycle system, wherein a cycling gas stream (otherwise known as a recycle stream or fluidizing medium) is heated in a reactor by heat of polymerization. The heat is removed from the cycling gas stream in another part of the cycle by a cooling system external to the reactor.
  • the cycling gas stream containing one or more monomers may be continuously cycled through a fluidized bed in the presence of a catalyst under reactive conditions.
  • the cycling gas stream is generally withdrawn from the fluidized bed and recycled back into the reactor. Simultaneously, polymer product may be withdrawn from the reactor and fresh monomer may be added to replace the polymerized monomer.
  • the reactor pressure in a gas phase process may vary from about 100 psig to about 500 psig, or from about 200 psig to about 400 psig or from about 250 psig to about 350 psig, for example.
  • the reactor temperature in a gas phase process may vary from about 30°C to about 120°C, or from about 60°C to about 115°C, or from about 70°C to about 110°C or from about 70°C to about 95°C, for example.
  • Slurry phase processes generally include forming a suspension of solid, particulate polymer in a liquid polymerization medium, to which monomers and optionally hydrogen, along with catalyst, are added.
  • the suspension (which may include diluents) may be intermittently or continuously removed from the reactor where the volatile components can be separated from the polymer and recycled, optionally after a distillation, to the reactor.
  • the liquefied diluent employed in the polymerization medium may include a C3 to C7 alkane (e.g., hexane or isobutane), for example.
  • the medium employed is generally liquid under the conditions of polymerization and relatively inert.
  • a bulk phase process is similar to that of a slurry process with the exception that the liquid medium is also the reactant (e.g. t monomer) in a bulk phase process.
  • a process may be a bulk process, a slurry process or a bulk slurry process, for example.
  • a slurry process or a bulk process may be carried out continuously in one or more loop reactors.
  • the catalyst as slurry or as a dry free flowing powder, may be injected regularly to the reactor loop, which can itself be filled with circulating slurry of growing polymer particles in a diluent, for example.
  • hydrogen may be added to the process, such as for molecular weight control of the resultant polymer.
  • the loop reactor may be maintained at a pressure of from about 27 bar to about SO bar or from about 35 bar to about 45 bar and a temperature of from about 38°C to about 121°C, for example.
  • Reaction heat may be removed through the loop wall via any method known to one skilled in the art, such as via a double-jacketed pipe or heat exchanger, for example.
  • polymerization processes may be used, such as stirred reactors in series, parallel or combinations thereof, for example.
  • the polymer may be passed to a polymer recovery system for further processing, such as addition of additives and or extrusion, for example.
  • the multicomponent catalyst has an activity of from 5 kg g/hr to 25 kg/g/hr, or from 7 kg g hr to 17 kgg hr, or from 9 kg/g/hr to 15 kg/g hr, or from 11 kg/g/hr to 13 kg/g hr.
  • the multicomponent catalyst has a conversion of propylene of from 15 to 60%, or from 20 to 50%, or from 25 to 45%.
  • the polymers (and blends thereof) formed via the processes described herein may include, but are not limited to, polypropylene (e.g., syndiotactic, atactic and isotactic) and polypropylene copolymers, for example.
  • the polymers can have a variety of compositions, characteristics and properties. At least one of the advantages of the multicomponent catalysts is that the process utilized can be tailored to form a polymer composition having a desired set of properties. A non-limiting discussion of such properties follows.
  • the polymers include propylene polymers.
  • the propylene polymer includes isotactic polypropylene.
  • the propylene polymers may include propylene homopolymers or copolymers.
  • the terms "propylene polymer” or “polypropylene” may refer to propylene homopolymers or those polymers composed primarily of propylene and limited amounts of other comonomers, such as ethylene, wherein the comonomer makes up less than 0.5 wt.% or less than about 0.1 wt.% by weight of polymer, or to propylene copolymers composed primarily of propylene and a comonomer, such as ethylene, wherein the comonomer makes up from 1 wt% to 20 wt%, or from 3 wt% to 15 wt% of the polymer.
  • the propylene polymer may include ethylene-propylene rubber (EPR).
  • EPR ethylene-propylene rubber
  • the propylene polymer exhibits a melt flow rate of from 1 to greater than 200 g/10 min., or from 10 to 150 g 10 min., or from 20 to 100 g 10 min., or from 30 to 80 g 10 min., or from 40 to 65 g 10 min.
  • the melt flow rate may also be from 0.02 to 10 g 10 min. or from 2 g/10 min. to 5 g 10 min.
  • the propylene polymer exhibits a melting point of from 120 to 160 °C, or from 150 to 155°C, or from 140 to 145 °C.
  • the propylene polymer exhibits a xylene solubles level from 0.20 to 10.00 wt%, or from 0.25 to 1.20 wt%, or from 0.35 to 0.80 wt%, or from 0.40 to 0.65 wt%, or from 0.45 to 0.60 wt%.
  • the polymers and blends thereof are useful in applications known to one skilled in the art, such as forming operations (e.g., film, sheet, pipe and fiber extrusion and co-extrusion as well as blow molding, injection molding and rotary molding).
  • Films include blown or cast films formed by co-extrusion or by lamination useful as shrink film, cling film, stretch film, sealing films, oriented films, snack packaging, heavy duty bags, grocery sacks, baked and frozen food packaging, medical packaging, industrial liners, and membranes, for example, in food-contact and non-food contact application.
  • Fibers include melt spinning, solution spinning and melt blown fiber operations for use in woven or non-woven form to make filters, diaper fabrics, medical garments and geotextiles, for example.
  • Extruded articles include medical tubing, wire and cable coatings, geomembranes and pond liners, for example. Molded articles include single and multi-layered constructions in the form of bottles, tanks, large hollow articles, rigid food containers and toys, for example.
  • metallocene type "m” refers to rac-dimethylsilanylbis(2- methyl-4-phenyl-1-indenyl)zirconium dichloride.
  • metallocene type "n” refers to rac-dimethylsilanylbis(2- methyl-1-indenyl)zirconium dichloride.
  • the m and n catalysts were first prepared separately with 1.0 wt% metallocene deposition/cationization in toluene using a P-10 silica MAO support prepared by reaction of MAO with silica in toluene at 115 °C for 4 hours.
  • the mineral oil suspended catalysts were then mixed with different weight ratio under nitrogen at room temperature. This catalyst blend is referred to in the Figures and Tables as *m' + 'n' as the catalyst components are individually supported and then blended.
  • the polymerization conditions were 20 mg supported catalyst, ca. 720 g. propylene, 40 mg TEAL as scavenger in 2 L Autoclave Zipper reactor with initial hydrogen concentration varied (depending on reaction conditions as listed in the Tables or in the Figures), at 70 °C for 1 hour.
  • Figures 1- 7 show ( m + n' catalysts. As can be seen in Figure 1, the catalyst activity increased from 14 to between 22 and 26 kg g/hr, and the fluff bulk density increased from 0.40 to 0.44 g/cc with an increase in the amount of n used. As shown in Figure 2, controlling the content of m catalyst results in control of the resins melt flow. Figure 3 and
  • Table 1 show that a 2.0 wt% catalyst loading is a good compromise based on economics.
  • Figures 8-12 show 'm + n' catalysts
  • Figures 13-14 show both 'm + n' and W +
  • the catalyst used comprised of a 2% metallocene loading on 0.7/1 MAO on P10 silica.
  • the metallocene component was a 1.5:1 wt% ratio of m and n.
  • Table 4 provided the screening results of m + n catalyst for mRCP.
  • the m catalyst usually incorporates about 1% ethylene for every 1 % in the feed under these conditions.
  • the decrease in the melting temperature of the resulting copolymer also reflected the high level of ethylene incorporation.
  • 1 wt% ethylene in copolymers reduces the melting temperature about 5-6 °C.
  • Molecular weight distribution was not sensitive to ethylene concentration (all were narrow) but this is typically not the case for multi-site catalysts.
  • the xylene soluble fraction was low for the homopolymer and as expected increased dramatically as the melting temperature of the resin approached 110 °C. Polypropylene resins with low melting temperature ( ⁇ 110 °C), low crystallinity level ( ⁇ 15 %) and slow crystallization rates are by their nature, soluble in xylene.
  • N catalyst incorporates ethylene much more readily than the ( m' catalyst and very similar to what is seen with AR35 and CpFlu-type metallocenes ( Figure 16).
  • Figure 18 As seen with the 'm' catalyst as well as copolymers produced by AR35, once the melting temperature of the copolymer approaches 110 °C, the amount of polymer soluble in xylene increases substantially (Figure 18).
  • the difference in copolymerization behavior of the M+N catalyst is further illustrated by considering the melting temperature of the copolymer produced as a function of ethylene wt% in the feed.
  • the N catalyst in the presence of 1 wt% ethylene in the feed produces a melting temperature of 105 °C with an ethylene level (measured by IR) of 8.4 wt%.
  • the 'm' catalyst produces a melting temperature of about 145 °C.
  • the M+N catalyst produces mRCP with a melting temperature that closely resembles that of the 'm' catalyst since this is the dominant crystalline phase in the polymer.
  • the fraction of polymer produced by the 'N' portion should be substantially less crystalline than that produced by the 'M' portion and consequently, one would expect a deviation from the standard T m vs crystallinity plot for mRCP produced in the lab with M+N compared to compositionally pure materials (similar to what is observed with ICP materials).
  • a plot of T m vs crystallinity indeed shows substantial deviation (Figure 17) from the typical relationship observed for compositionally pure materials.
  • MRCP produced with the M+N catalyst has lower crystallinity at a given T m than other materials.

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Abstract

L'invention concerne d'une manière générale des systèmes de catalyseur multi-composants, des procédés de polymérisation et des mélanges en réacteur formés par les procédés. Le système de catalyseur multi-composants comprend d'une manière générale un premier composant de catalyseur et un second composant de catalyseur, le second composant de catalyseur étant différent du premier composant de catalyseur.
EP12877323.1A 2011-06-16 2012-06-13 Systèmes de catalyseur de métallocène multi-composants pour la fabrication de mélanges en réacteur de polypropylène Withdrawn EP2794688A4 (fr)

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PCT/US2012/042201 WO2013176686A1 (fr) 2012-05-21 2012-06-13 Systèmes de catalyseur de métallocène multi-composants pour la fabrication de mélanges en réacteur de polypropylène

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