CA2547396A1 - High tear films from hafnocene catalyzed polyethylenes - Google Patents

Abstract

A polyethylene film having a balance of improved physical and mechanical properties and a method for making the same are provided. In one aspect, the film includes a 1% secant modulus of greater than 25,000 psi, a dart impact resistance'of greater than 500 g/mil, and a MD tear strength of greater than 500 g/mil. In one aspect, the method comprises reacting ethylene derived units and a comonomer in the presence of a hafnium-based metallocene at a temperature of from 70~C and 90~C, an ethylene partial pressure of from 120 psia and 260 psia, and a comonomer to ethylene ratio of from 0.01 to 0.02 to produce an ethylene based polymer. The method further comprises extruding the ethylene based polymer at conditions sufficient to produce a polyethylene film comprising a secant modulus of greater than 25,000 psi, a dart impact resistance of greater than 500 g/mil, and a MD tear strength of greater than 500 g/mil.

Description

-1_ HIGH TEAR FILMS FROM HAFNOCENE CATALI'ZED POLYETHYLENES
BACKGROUND OF THE INVENTION
Field of the Invention [0001] The present invention relates to films that exhibit a superior balance of physical properties. The films are produced with polyethyhenes having a broad composition distribution (CD) and molecular weight distribution (MWD).
Description of the Related Art [0002] Metallocene-catalyzed ethylene polymers are known to produce tough films measured in teams of dart drop impact strength (dart). Conventional Ziegler-Natta catalyzed linear low density polyethylenes (Z-N LLDPE) are known to have good processability, stiffness and tear strength, as measured by extruder pressures and motor load, 1 % secant madulus, and Ehnendorf tear strength. Ideally, a polyethylene resin would have Z-N LLDPE
processability and produce a film exhibiting a combination of metallocene like toughness and Ziegler-Natta like stiffness and tear strength. It is possible to improve the toughness of films (e.g. MD tensile strength) by increasing the amount of orientation in the machine direction during film blowing.
However, conventional knowledge in the polyethylene film art says that by increasing the machine direction (MD) orientation in films during manufacture of these films, other physical propeuties, such as MD tear strength, will decrease.

[0003] To this point, in Polymer En~ineerin~ and Science, mid-October 1994, ooh. 34, No. 19, the disclosure of which is incorporated herein by reference, the authors discuss processing structure properties relationships in polyethylene bloom film. The authors suggest that MD
Elmendorf tear is found to be inversely related to drawdown ratio and MD
shrinkage.
[0004j Further, in Poker, 41 0000) 9205-9217, the disclosure of which is incorporated herein by reference, the authors suggest that at high MD extension rates, a greater number of molecules will be oriented along the MD prior to the onset of crystallization, and that this is detrimental from a MD tear performance perspective.
[0005] Metahhocene catalyst components can be combined to form blend compositions as described in PCT publication WO 90/03414 published April 5, 1990, the disclosure of which is incorporated herein by reference. Also mixed metalhocenes as described in U.S.
Patent Nos.

4,937,299 and 4,935,474, the disclosure of both wluch are incorporated herein by reference, can be used to produce polymers having a broad molecular weight distribution and/or a multimodal molecular weight distribution.
[0006] LT.S. 5,514,455 suggests that a reduction in gauge of polyethylene films results in an increase in tear values. This document employs a titanium magnesium catalyst for polyethylene production and includes titanium residues in the polyethylene.
Reported values of Elmendorf machine direction (MD) tear to transverse direction (TD) tear, are in the range of 0.1-0.3 far inventive examples.
[0007] U.S. 5,744,551, the disclosure of which is incorporated herein by reference, suggests a balance of tear property improvement. This document also employs a titanium magnesium catalyst for polyethylene production and includes titanium residues in the polyethylene.
Further, the MD/TD tear ratios are in the range of 0.63-0.80 for inventive examples.
(0008] U.S. 5,382,630, the disclosure of which is incorporated herein ~by reference, discloses linear ethylene interpolymer blends made from components that can have the same molecular weight but different comonomer contents, or the same comonomer contents but different molecular weights, or comonomer contents which increase with molecular weight.
US

5,382,630 suggests multimodal polyethylene blends for which tear strength can be controlled.
However, this document uses only intrinsic tear, and is silent on Elmendorf MD/TD tear ratios and on any other values but intrinsic tear.
[0009] Also, in LT.S. 6,242,545 and U.S. 6,248,845 as well as provisional applications USSN
60/306,503 filed July 19, 2001 and 60/306,903 filed July 19, 2001, the disclosures of all which are incorporated herein by reference, the patentees/applicants of these documents reported production of either broad composition distribution, narrow molecular weight, or broad C0111pC~Sltloll distribution, relatively broad molecular weight distribution polyethylenes.
However, these documents show an improvement in cast film MD tear, but no appreciable improvement for blown film.
[0010] There is a need, therefore, for a polyolefin film, more specifically a blown polyethylene filin, that has high machine direction tear (MD tear) and/or high transverse direction tear (TD
tear), and/or high dart drop impact resistance (dart), made fiom a polyethylene that is easier to process than prior metallocene catalyst produced linear low density polyethylenes (mLLDPE).

In other words it is desirable to have the processability, stiffness and tear strength of a ZN-LLDPE combined with the dart impact strength of a mLLDPE.
SUMMARY OF THE INVENTION
[0011] A polyethylene film having a balance of improved physical and mechanical properties and a method for making the same are provided. In one aspect, the film includes a 1 % secant modulus of greater than 25,000 psi, a dart impact resistance of greater than 500 g/mil, and a MD tear strength of greater than 500 g/mil. In another aspect, the film comprises an ethylene based polymer produced in the presence of a hafnium-based metallocene within a gas phase reactor operated at a temperature of from 70°C and 90°C and at an ethylene partial pressure of fiom 120 psia and 260 Asia.
[0012] In yet another aspect, a film is provided by extruding an ethylene based polymer produced in the presence of a hafnium-based metallocene within a gas phase reactor operated at a temperature of from 70°C and 90°C and at an ethylene partial pressure of from 120 psia and 260 psia, wherein the film comprises a 1% secant modulus of greater than 25,000 psi, a dart impact resistance of greater than 500 g/mil, and a MD tear strength of greater than 500 g/mil.
[0013] The method for producing a film having a balance of improved physical and mechanical properties comprises reacting ethylene derived units and a comonomer in the presence of a hafnium-based metallocene at a temperature of from 70°C
and 90°C, an ethylene pautial pressure of from 120 psia and 260 psia, and a comonomer to ethylene ratio of from 0.01 to 0.02 to produce an ethylene based polymer. The method further comprises extruding the ethylene based polymer at conditions sufficient to produce a polyethylene film comprising a 1% secant modulus of greater than ''5,000 psi, a dart impact resistance of greater than 500 g/mil, and a MD tear strength of greater than 500 g/mil.
Detailed Description [0014] Films having a unique balance of machine direction (MD) and transverse direction (TD) tear, and/or a simultaneously increasing MD tear with increasing MD shrinkage are provided.
It has been surprisingly found that these improved properties are a result of a polymer having a broad comonomer distribution (CD) and molecular weight distribution (MWD).
Further, it has been surprisingly found that the comonomer distribution and molecular weight distribution of the polymer are produced by controlling either the reactor temperature or ethylene partial pressure or both in the presence of a hafiiium-based metallocene catalyst ("metallocene" or "hafnocene") or hafnocene catalyst system.
[0015] A ''catalyst system" as used herein may include one or more polymerization catalysts, activators, supports/carriers, or any combination thereof, and the terms ''catalyst" and "catalyst system" are intended to be used interchangeably herein. The terns "supported"
as used herein refers to one or more compounds that are deposited on, contacted with, vaporized with, bonded to, or incorporated within, adsorbed or absorbed in, or on, a support or carrier. The terns "support" or "carrier" for purposes of this specification are used interchangeably and are any support material, preferably a porous support material, including inorganic or organic support materials. Non-limiting examples of inorganic support materials include inorganic oxides and inorganic chlorides. Other carriers include resinous support materials such as polystyrene, functionalized or crosslinked organic supports, such as polystyrene, divinyl benzene, polyolefms, or polymeric compounds, zeolites, talc, clays, or any other organic or inorganic support material a.nd the like, or mixtures thereof.
Catalyst Components and Catalyst Systems [0016] Hafiiocenes are generally described throughout in, for example, 1 & 2 METALLOCENE-BASED PoLYOLEFINS (John Scheirs ~ W. Kaminsky eds., John Wiley & Sons, Ltd.
2000); G.G.
Hlatky in 181 COORDINATION CHEM. REV. 243-296 (1999) and in particular, for use in the synthesis of polyethylene in 1 METALLOCENE-BASED POLYOLEFINS 261-377 (2000).
The hafnocene compounds as described herein include "half sandwich" and "full sandwich"
compounds having one or more Cp ligands (cyclopentadienyl and ligands isolobal to cyclopentadienyl) bound to a hafnium atom, and one or more leaving groups) bound to the hafnium atom. Hereinafter, these compounds will be referred to as "hafnocences,"
"metallocenes," or "metallocene catalyst components". The hafnocene may be supported on a support material in a particular embodiment as described further below, and may be supported with or without another catalyst component or components.
[0017] As used herein, in reference to Periodic Table "Groups" of Elements, the "new"
niunbering scheme for the Periodic Table Groups are used as in the CRC
HANDBOOK OF
CHEMISTRY AND PHYSICS (David R. Lide ed., CRC Press 81St ed. 2000).
[0018] The Cp ligands are one or more rings or ring system(s), at least a portion of which includes ~-bonded systems, such as cycloalkadienyl ligands and heterocyclic analogues. The -5_ rings) or ring systems) typically comprise atoms selected from the group consisting of Groups 13 to 16 atoms, and more particularly, the atoms that make up the Cp ligands are selected from the group consisting of carbon, nitrogen, oxygen, silicon, sulfur, phosphorous, germanium, boron and aluminum and combinations thereof, wherein carbon makes up at least 50% of the ring members. Even more particularly, the Cp ligand(s) are selected from the group consisting of substituted and unsubstituted cyclopentadienyl ligands and ligands isalobal to cyclopentadienyl, non-limiting examples of which include cyclopentadienyl, indenyl, fluorenyl and other structures. Further non-limiting examples of such ligands include cyclopentadienyl, cyclopentaphenanthreneyl, indenyl, benzindenyl, fluorenyl, octahydrofluorenyl, cyclooctatetraenyl, cyclopentacyclododecene, phenanthrindenyl, 3,4-benzofluorenyl, 9-phenylfluorenyl, 8-H-cyclopent[a]acenaphthylenyl, 7H-dibenzofluorenyl, indeno[1,~-9]anthrene, thiophenoindenyl, thiophenofluorenyl, hydrogenated versions thereof (e.g., 4,5,6,7-tetrahydroindenyl, or "H~Ind"), substituted versions thereof (as described in more detail below), and heterocyclic versions thereof.
[00~ 9] In one aspect of the invention, the one or more metallocene catalyst components of the invention are represented by the formula (I):
CpACpBHfX" (I) [0020] wherein each X is chemically bonded to Hf; each Cp group is chemically bonded to Hf;
and n is 0 or an integer from 1 to 4, and either 1 or 2 in a particular embodiment.
[0021] The ligands represented by CpA and CpB in formula (I) may be the same or different cyclopentadienyl ligands or ligands isolobal to cyclopentadienyl, either or both of which may contain heteroatoms and either or both of which may be substituted by a group R. In one embodiment, CpA and CpB are independently selected from the group consisting of cyclopentadienyl, indenyl, tetrahydroindenyl, fluorenyl, and substituted derivatives of each.
[0022] Independently, each CpA and CpB of formula (I) may be unsubstituted or substituted with any one or combination of substituent groups R. Non-limiting examples of substituent groups R as used in structure (I) include hydrogen radicals, alkyls, alkenyls, alkynyls, cycloalkyls, aryls, acyls, aroyls, alkoxys, aryloxys, alkylthiols, dialkylamines, alkylamidos, alkoxycarbonyls, .aryloxycarbonyls, carbomoyls, alkyl- and dialkyl-carbamoyls, acyloxys, acylaminos, aroylaminos, and combinations thereof.

[0023] More particular non-limiting examples of alkyl substituents R
associated with formula (I) through (V) include methyl, ethyl, propyl, butyl, pentyl, hexyl, cyclopentyl, cyclohexyl, benzyl, phenyl, methylphenyl, and tent-butylphenyl groups and the like, including all their isomers, for example tertiary-butyl, isopropyl, and the like. Other possible radicals include substituted alkyls and aryls such as, for example, fluoromethyl, fluroethyl, difluroethyl, iodopropyl, bromohexyl, chlorobenzyl and hydrocarbyl substituted organometalloid radicals including trimethylsilyl, trimethylgermyl, methyldiethylsilyl and the like;
and halocarbyl-substituted organometalloid radicals including tris(trifluoromethyl)silyl, methylbis(difluoromethyl)silyl, bromomethyldimethylgemayl and the like; and disubstituted boron radicals including dimethylboron for example; and disubstituted Group 15 radicals including dimethylamine, dimethylphosphine, diphenylamine, methylphenylphosphine, Group 16 radicals including methoxy, ethoxy, propoxy, phenoxy, methylsulfide and ethylsulfide.
Other substituents R include olefins such as but not limited to olefinically unsaturated substituents including vinyl-terminated ligands, for example 3-butenyl, ?-propenyl, 5-hexenyl and the like. In one embodiment, at least two R groups, two adjacent R groups in one embodiment, are joined to form a ring structure having from 3 to 30 atoms selected from the group consisting of carbon, nitrogen, oxygen, phosphorous, silicon, germanium, aluminum, boron and combinations thereof. Also, a substituent group R group such as 1-butanyl may form a bonding association to the hafnium atom.
[0024] Each ~i in the formula (I) above and for the formulas/structures (II) through (V) below is independently selected fiom the group consisting of: any leaving group in one embodiment;
halogen ions, hydrides, C~ to Cl2 alkyls, C2 to C12 alkenyls, C6 to C~2 aryls, C7 to C~o alkylaryls, C1 to C1~ alkoxys, C6 to C16 aryloxys, C~ to C18 alkylaryloxys, C1 to CIA
fluoroalkyls, Cb to Cla fluoroaryls, and C~ to C~2 heteroatom-containing hydrocarbons and substituted derivatives thereof in a more particular embodiment; hydride, halogen ions, C1 to Ce alkyls, C~ to C6 alkenyls, C7 to Cls alkylaryls, C1 to Cd alkoxys, C6 to C14 aryloxys, C7 to C1~ alkylaryloxys, CI
to C6 alkylcarboxylates, C1 to Cn fluorinated alkylcarboxylates, C6 to C1~
arylcarboxylates, C7 to C18 alkylarylcarboxylates, C1 to C6 fluoroalkyls, C~ to Ce fluoroalkenyls, and C~ to C~$
fluoroalkylaryls in yet a more particular embodiment; hydride, chloride, fluoride, methyl, phenyl, phenoxy, benzoxy, tosyl, fluoromethyls and fluorophenyls in yet a more particular embodiment; C1 to C1~ alkyls, C2 to C12 alkenyls, C6 to C~2 aryls, C~ to C2~
alhylaryls, substituted C1 to C1? allyls, substituted C6 to C~~ aryls, substituted C~ to C2o alkylaryls and C1 to C1~ heteroatom-containing allcyls, C1 to C~2 heteroatom-containing aryls and C1 to C~Z

heteroatom-containing alkylaryls in yet a more particular embodiment;
chloride, fluoride, C1 to C6 alkyls, C2 to C6 alkenyls, C7 to Cls alkylaryls, halogenated C~ to C6 alkyls, halogenated C2 to Cb alkenyls, and halogenated C7 to CAS alkylaryls in yet a more particular embodiment;
fluoride, methyl, ethyl, propyl, phenyl, methylphenyl, dimethylphenyl, trimethylphenyl, fluoromethyls (mono-, di- and trifluoromethyls) and fluorophenyls (mono-, di-, tri-, tetra- and pentafluorophenyls) in yet a more particular embodiment.
[0025] Other non-limiting examples of X groups in formula (I) include amines, phosphines, ethers, carboxylates, dimes, hydrocarbon radicals having from 1 to 20 carbon atoms, fluorinated hydrocarbon radicals (e.g., -C6F5 (pentafluorophenyl)), fluorinated alkylcarboxylates (e.g., CF~C(O)O-), hydrides and halogen ions and combinations thereof.
Other examples of X ligands include alkyl groups such as cyclobutyl, cyclohexyl, methyl, heptyl, tolyl, trifluoromethyl, tetramethylene, pentamethylene, methylidene, methyoxy, ethyoxy, propoxy, phenoxy, bis(N-methylanilide), dimethylamide, dimethylphosphide radicals and the like. In one embodiment, two or more X's form a part of a fused ring or ring system.
[0026] In another aspect, the metallocene catalyst component includes those of formula (I) where CpA .and Cpa are bridged to each other by at least one bridging group, (A), such that the structure is represented by formula (II):
CpA(A)CpBHf~" (II) [0027] These bridged compounds represented by formula (II) are known as "bridged metallocenes .". CpA, CpB, X and n in structure (II) are as defined above for formula (I); and wherein each Cp ligand is chemically bonded to Hf, and (A) is chemically bonded to each Cp.
Non-limiting examples of bridging group (A) 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 and tin atom and combinations thereof;
wherein the heteroatom may also be CI to C12 alkyl ox aryl substituted to satisfy neutral valency. The bridging group (A) may also contain substituent groups R as defined above (for formula (I)) including halogen radicals and iron. More particular non-limiting examples of bridging group (A) are represented by C~ to Cd alkylenes, substituted C1 to C6 alkylenes, oxygen, sulfur, R'~C=, R'ZSi=, -Si(R')~Si(R'~)-, R'2Ge=, R'P= (wherein "--"
represents two chemical bonds), where R' is independently selected from the group consisting of hydride, hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, hydrocarbyl--s-substituted organometalloid, halocarbyl-substituted organometalloid, disubstituted boron, disubstituted Group 1 S atoms, substiW ted Group 16 atoms, and halogen radical; and wherein two or more R' may be joined to form a ring or ring system. In one embodiment, the bridged metallocene catalyst component of formula (II) has two or more bridging groups (A).
[0028] Other non-limiting examples of bridging group (A) 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 moieties wherein the Si atom is replaced by a Ge or a C atom; dimethylsilyl, diethylsilyl, dimethylgermyl and diethylgennyl.
[0029] In another embodiment, bridging group (A) may also be cyclic, comprising, for example 4 to 10, 5 to 7 ring members in a more particular embodiment. The ring members may be selected from the elements mentioned above, from one or more of B, C, Si, Ge, N and O in a particular embodiment. Non-limiting examples of ring strucW res which may be present as or part of the bridging moiety are cyclobutylidene, cyclopentylidene, cyclohexylidene, cyclohept5rlidene, cyclooctylidene and the corresponding rings where one or two carbon atoms are replaced by at least one of Si, Ge, N and O, in particular, Si and Ge. The bonding arrangement between the ring and the Cp groups may be either cis-, ~trans-, or a combination.
[0030] The cyclic bridging groups (A) may be saturated or unsaturated and/or carry one or more substituents and/or be fused to one or more other ring structures. If present, the one or more substituents are selected from the group consisting of hydrocarbyl (e.g., alkyl such as methyl) and halogen (e.g., F, Cl) in one embodiment. The one or more Cp groups which the above cyclic bridging moieties may optionally be fused to may be saturated or unsaturated a.nd are selected from the group consisting of those having 4 to 10, more particularly 5, 6 or 7 ring members (selected from the group consisting of C, N, O and S in a particular embodiment) such as, for example, cyclopentyl, cyclohexyl and phenyl. Moreover, these ring structures may themselves be fused such as, for example, in the case of a naphthyl group.
Moreover, these (optionally fused) ring structures may carry one or more substituents.
Tllustrative, non-limiting examples of these substituents are hydrocarbyl (particularly alkyl) groups and halogen atoms.

_g_ [0031] The ligands CpA and CpB of formula (I) and (II) are different from each other in one embodiment, and the same in another embodiment.
[0032] Some specific, non-limiting examples of hafnocenes include bis(n-propyl cyclopentadienyl) hafnium dichloride, bis(n-propyl cyclopentadienyl) hafnium difluoride, bis(n-propyl cyclopentadienyl) hafnium dimethyl, bis(n-propyl cyclopentadienyl) hafnium dihydride,bis(2-propenylcyclopentadienyl) hafnium dichloride, bis(2-propenylcyclopentadienyl) hafnium difluoride, bis(2-propenylcyclopentadienyl) hafnium dimethyl, bis(n-butyl cyclopentadienyl) hafnium dichloride, bis(n-butyl cyclopentadienyl) hafnium difluoride, bis(n-butyl cyclopentadienyl) hafnium dimethyl, bis(3-butenylcyclopentadienyl) hafnium dichloride, bis(3-butenylcyclopentadienyl) hafnium difluoride, bis(3-butenylcyclopentadienyl) hafnium dimethyl, bis(n-pentyl cyclopentadienyl) hafnium dichloride, bis(n-pentyl cyclopentadienyl) hafiuum difluoride, bis(n-pentyl cyclopentadienyl) hafnium dimethyl, (n-propyl cyclopentadienyl)(n-butyl cyclopentadienyl) hafnium dichloride or dimethyl, bis(trimethylsilylmethylcyclopentadienyl) hafnium dichloride, bis[(2-trimethylsilyl-ethyl)cyclopentadienyl] hafnimn dichloride or dimethyl, bis(trimethylsilyl cyclopentadienyl) hafnium dichloride or dimethyl or dihydride, bis(2-n-propyl indenyl) hafnium dichloride or dimethyl, bis(2-n-butyl indenyl) hafnium dichloride or dimethyl, dimethylsilyl bis(n-propyl cyclopentadienyl) hafnium dichloride or dimethyl, dimethylsilyl bis(n-butyl cyclopentadienyl) hafnium dichloride or dimethyl, bis(9-n-propyl fluorenyl) hafnium dichloride or dimethyl bis(9-n-butyl fluorenyl) hafnium dichloride or dimethyl, (9-n propyl fluorenyl)(2-n-propyl indenyl) hafnium dichloride or dimethyl, bis(1,2-n-propyl, methyl cyclopentadienyl) hafnium dichioride or dimethyl, bis(1,3-n-propylmethylcyclopentadienyl) hafnium dichloride, (n-propyl cyclopentadienyl) (1,3-n-propyl, n-butyl cyclopentadienyl) hafnium dichloride or dimethyl and the like.
[0033] Typically, the catalyst described above is activated towards olefin polymerization using one or more activators. As used herein, the terns "activator" is defined to be any compound or combination of compounds, supported or unsuppouted, which can activate a single-site catalyst compound, such as a metallocene, by creating a cationic species from the catalyst component.
Typically, this involves the abstraction of at least one leaving group from the metal center of the catalyst component. Embodiments of such activators include Lewis acids such as cyclic or oligomeric poly(hydrocarbylaluminum oxides) and so called non-coordinating activators ("NCA") (alternately, "ionizing activators" or "stoichiometric activators"), or any other compound that can convent a neutral metallocene catalyst component to a metallocene ration that is active with respect to olefin polymerization.
[0034] More particularly, it is within the scope of this invention to use Lewis acids such as alumoxane (e.g., "MAO"), modified alumoxane (e.g., "TIBAO"), and alkylaluminum compounds as activators, aaid/or ionizing activators (neutral or ionic) such as tri (n-butyl)armnonium tetrakis(pentafluorophenyl)boron and/or a trisperfluorophenyl boron metalloid precursors. MAO and other aluminum-based activators are well known in the art.
Ionizing activators are well known in the art and are described by, for example, Eugene You-Xian Chen & Tobin J. Marks, Coeatalvsts for Metal-Catalyzecl Olefin Polvr~uerizcrtiorz:
Activators, Actimationa P~°ocesses, aiacl St~°ucture-Activity Relationships 100(4) CHEMICAL
REVIEWS 1391-1434 (2000). The activators may be associated with or bound to a support, either in association with the catalyst component (e.g., metallocene) or separate from the catalyst component, such as described by Gregory G. Hlatky, Heterogeneous Single-Site Catalvsts for' OIeyZ Polyrr~er~ization 100(4) CHEMICAL REVIEWS 1347-1374 (?000).
[0035] The aluminum alkyl (''alkylaluminum") activator may be described by the formula A1R'3, wherein R~ is selected from the group consisting of C~ to Coo alkyls, C~ to C~~ alkoxys, halogen (chlorine, fluorine, bromine) C6 to C2o aryls, C7 to C25 alkylaryls, and C7 to CZs arylalkyls. Non-limiting examples of aluminwn alkyl compounds which may be utilized as activators for the catalyst precursor compounds for use in the methods of the present invention include trimethylaluminum, triethylaluminum, triisobutylaluminum, tri-n-hexylaluminum, tri-n-octylaluminum and the like.
[0036] In general, the activator and catalyst are combined in mole ratios of activator to catalyst component from 1000:1 to O.I:l, and from 300:1 to 1:1 in another embodiment, and from 150:1 to 1:1 in yet another embodiment, and from 50:1 to 1:1 in yet another embodiment, and from 10:1 to 0.5:1 in yet another embodiment, and from 3:1 to 0.3:1 in yet another embodiment, wherein a desirable range may include any combination of any upper mole ratio limit with any lower mole ratio limit described herein. When the activator is a cyclic or oligomeric poly(hydrocarbylaluminum oxide) (e.g., ''MAO"), the mole ratio of activator to catalyst component ranges from 2:1 to 100,000:1 in one embodiment, and from 10:1 to 10,000:1 in another embodiment, and from 50:1 to 2,000:1 in yet another embodiment. For a more complete discussion of exemplary hafnocence catalysts and activators, please refer to commonly assigned U.S. Patent Nos. 6,242,545 and 6,248,845.
Polymerization Process [0037] The catalysts described above are suitable for use in any olefin prepolymerization or polymerization process or both. Suitable polymerization processes include solution, gas phase, slung phase and a high pressure process, or any combination thereof. A
desirable process is a gas phase polymerization of one or more one or more olefin monomers having from 2 to 30 carbon atoms, from 2 to 12 carbon atoms in another embodiment, and from ? to 8 carbon atoms in yet another embodiment. Other monomers useful in the process include ethylenically unsaturated monomers, diolefins having 4 to 18 carbon atoms, conjugated or nonconjugated dimes, polyenes, vinyl monomers and cyclic olefins. Non-limiting monomers may also include norbornene, norbornadiene, isobutylene, isoprene, vinylbenzocyclobutane, styrenes, alkyl substituted styrene, ethylidene norbornene, dicyclopentadiene and cyclopentene.
[0038] In a desirable embodiment, a copolymer of ethylene derived units and one or more monomers or comonomer is produced. The one or more comonomers are preferably an a-olefin having from 4 to 15 carbon atoms in one embodiment, and from 4 to 12 carbon atoms in another embodiment, and from 4 to 8 carbon atoms in yet another embodiment.
Preferably, the comonomer is 1-hexene.
[0039] Hydrogen gas is often used in olefin polymerization to control the final properties of the polyolefin, such as described in Polypropylene Handbook 76-78 (Hanser Publishers, 1996).
Increasing concentrations (paatial pressures) of hydrogen increase the melt flow rate (MFR) and/or melt index: (MI) of the polyolefin generated. The MFR or MI can thus be influenced by the hydrogen concentration. The amount of hydrogen in the polymerization can be expressed as a mole ratio relative to the total polymerizable monomer, for example, ethylene, or a blend of ethylene and hexane or propene. The amount of hydrogen used in the polymerization process of the present invention is an amount necessary to achieve the desired MFR or MI of the final polyoletin resin. In one embodiment, the mole ratio of hydrogen to total monomer (H2:monomer) is in a range of from greater than 0.0001 in one embodiment, and from greater than 0.0005 in another embodiment, and from greater than 0.001 in yet another embodiment, and less than 10 in yet another embodiment, and less than 5 in yet another embodiment, and less than 3 in yet another embodiment, and less than 0.10 in yet another embodiment, wherein a desirable range may comprise any combination of any upper mole ratio limit with any lower mole ratio limit described herein. Expressed another way, the amount of hydrogen in the reactor at any time may range to up to 5000 ppm, and up to 4000 ppm in another embodiment, and up to 3000 ppm in yet another embodiment, and between 50 ppm and 5000 ppm in yet another embodiment, and between 100 ppm and 2000 ppm in another embodiment [0040] Typically in a gas phase polymerization process a continuous cycle is employed wherein one part of the cycle of a reactor system, a cycling gas stream, otherwise known as a recycle stream or fluidizing medium, is heated in the reactor by the heat of polymerization.
This heat is removed from the recycle composition in another part of the cycle by a cooling system external to the reactor. Generally, in a gas fluidized bed process for producing polymers, a gaseous stream containing one or more monomers is continuously cycled through a fluidized bed in the presence of a catalyst under reactive conditions. The gaseous stream is withdrawn from the fluidized bed and recycled back into the reactor.
Simultaneously, polymer product is withdrawn from the reactor and fresh monomer is added to replace the polymerized monomer.
[0041] Further, it is conunon to use a staged reactor employing two or more reactors in series, wherein one reactor may produce, for example, a high molecular weight component and another reactor may produce a low molecular weight component. In one embodiment of the invention, the polyolefin is produced using a staged gas phase reactor. This and other commercial polymerization systems are described in, for example, 2 Metallocene-Based Polyolefins 366-378 (John Scheirs & W. ILaminsky, eds. John Wiley R, Sons, Ltd. 2000). Gas phase processes contemplated by the invention include those described in US
5,627,242, US
5,665,818 and US 5,677,375, and European publications EP-A- 0 794 200 EP-B1-0 649 992, EP-A- 0 802 20~ and EP-B- 634 421.
[0042] It has been surprising found that films having a unique balance of machine direction (MD) and transver se directions (TD) tear, and/or a simultaneously increasing MD tear with increasing MD shrinkage are produced when controlling the reactor temperature or ethylene partial pressure or both. Reactor temperature should vary between 60 and 120 °C, preferably between 65 and 100°C, more preferably between 70 and 90°C, and most preferably between 75 and 80°C. For purposes of this patent specification and appended claims the terms "polymerization temperature" and "reactor temperature" are interchangeable.

[0043] The ethylene partial pressure should vary between 80 and 300 Asia, preferably between 100 and 280 psia, more preferably between 120 and 260 psia, and most preferably between 140 and 240 Asia. More importantly, a ratio of comonomer to ethylene in the gas phase should vary from 0.0 to 0.10, preferably between 0.005 and 0.05, more preferably between 0.007 and 0.030, and most preferably between 0.01 and 0.02.
[0044] Reactor pressure typically varies from 100 psig (690 kPa) to 500 psig (3448 kPa). In one aspect, the reactor pressure is maintained witlun the range of from 200 psig (1379 kPa) to 500 psig (3448 kPa). In another aspect, the reactor pressure is maintained within the range of from 250 psig (1724 kPa) to 400 prig (2759 kPa).
Polymer Products [0045] The inventive polymers typically have a broad composition distribution as measured by Composition Distribution Breadth Index (CDBI) or solubilit5r distribution breadth index (SDBI). Further details of determining the CDBI or SDBI of a copolymer are known to those skilled in the art. See, for example, PCT Patent Application WO 93/03093, published February 18, 1993. Polymers produced using a catalyst system described herein have a CDBI less than 50%, more preferably less than 40%, and most preferably less than 30%. In one embodiment, the polymers have a CDBI of from 20% to less than 50%. In another embodiment, the polymers have a CDBI of from 20% to 35%. In yet another embodiment, the polymers have a CDBI of from 25% to 28%
[0046] Polymers produced using a catalyst system described herein have a SDBI
greater than 15°C, or greater than 16°C, or greater than 17°C, or greater than 18°C or greater than 20°C. In one embodiment, the polymers have a SDBI of from 18°C to 22°C.
In another embodiment, the polymers have a SDBI of from 18.7°C to 21.4°C. In another embodiment, the polymers have a SDBI of from 20°C to 22°C.
[0047] In one aspect, the polymers have a density in the range of from 0.86 g/cc to 0.97 g/cc, preferably in the range of from 0.90 g/cc to 0.950 g/cc, more preferably in the range of from 0.905 g/ce to 0.940 g/cc, and most preferably in the range of from 0.910 g/cc to 0.930 g/cc.
Density is measured in accordance with ASTM-D-1238.
[0048] The polymers have a molecular weight distribution, a weight average molecular weight to number average molecular weight (Mr~/M°) of greater than 2.0 to about 5, particularly greater than 2.5 to about 4.5, more preferably greater than about 3.0 to less than about 4.0, and most preferably from 3.2 to 3.8.
[0049] The polymers have a ratio of z-average molecular weight to weight average molecular weight of greater than 2.2 or greater than 2.5 or greater than 2.8. In one embodiment, this ratio is from about 2.2 and 3Ø In another embodiment, this ratio is from about 2.2 to about 2.8. In yet another embodiment, this ratio is from about 2.2 to about 2.5. In still yet another embodiment, this ratio is from about 2.4 to about 2.8.
[0050] The polymers made by the described processes can in certain embodiments have a melt index (MI) or (I2) as measured by ASTM-D-1238-E (190/2.16) in the range from 0.1 to 100 dg/min, preferably between 0.2 and 20 dg/min, more preferably between 0.3 and 5 dg/min, and most preferably between 0.5 and 1.5 dg/min.
[0051] In one embodiment, the polymers have a melt index ratio (I2r/I2) (I21 is measured by ASTM-D-1238-F) (190/21.6) of from 20 to less than 50. The polymers, in a preferred embodiment, have a melt index ratio (h~/I2) of from greater than 22, more preferably greater than 25, most preferably greater that 30.
[0052] The polymers may be blended and/or coextnided with any other polymer.
Non-limiting examples of other polymers include linear low density polyethylenes, elastomers, plastomers, high pressure low density polyethylene, high density polyethylenes, polypropylenes and the like.
Compounding, Processing and Articles Therefrom [0053] The polymers produced may also be blended with additives to fornz compositions that can then be used in articles of manufacture. Those additives include antioxidants, nucleating agents, acid scavengers, plasticizers, stabilizers, anticorrosion agents, blowing agents, other ultraviolet light absorbers such as chain-breaking antioxidants, etc., quenchers, antistatic agents, slip agents, pigments, dyes and fillers and cure agents such as peroxide. These and other common additives in the polyolefm industry may be present in polyolefin compositions from 0.01 to 50 wt% in one embodiment, and from 0.1 to 20 wt% in another embodiment, and from 1 to 5 wt% in yet another embodiment, wherein a desirable range may comprise any combination of any upper W% limit with any lower wt% limit.

[0054] In particular, antioxidants and stabilizers such as organic phosphites and phenolic antioxidants may be present in the polyolefin compositions from 0.001 to 5 wt%
in one embodiment, and from 0.01 to 0.8 wt% in another embodiment, and from 0.02 to 0.5 wt% in yet another embodiment. Non-limiting examples of organic phosphites that are suitable are tris(2,4-di-tert-butylphenyl)phosphite (IRGAFOS 168) and tris (nonyl phenyl) phosphite (WESTON 399) Non-limiting examples of phenolic antioxidants include octadecyl 3,5 di-t-butyl-4-hydroxyhydrocimzamate (IRGANO~ 1076) and pentae.rytllrityl tetrakis(3,5-di-tert-butyl-4-hydroxyphenyl) propionate (IRGANOX 1010); and 1,3,5-Tri(3,5-di-tert-butyl-4-hydroxybenzyl-isocyanurate (IRGANO~i 3114).
[0055] Fillers may be present from 0.1 to 50 wt% in one embodiment, and from 0.1 to 25 wt%
of the composition in another embodiment, and from 0.2 to 10 wt% in yet another embodiment.
Desirable tillers include but not limited to tltalllu111 dioxide, silicon carbide, silica (and other oxides of silica, precipitated or not), antimony oxide, lead carbonate, zinc white, lithopone, zircon, corundum, spinel, apatite, Barytes powder, barium sulfate, magnesiter, carbon black, dolomite, calcium carbonate, talc and hydrotalcite compounds of the ions Mg, Ca, or Zn with Al, Cr or Fe and C03 and/or HP04, hydrated or not; qual-tz powder, hydrochloric magnesium carbonate, glass fibers, clays, alumina, and other metal oxides and carbonates, metal hydroxides, chrome, phosphorous and brominated flame retardants, antimony trioxide, silica, silicone, and blends thereof. These fillers may particularly include any other fillers and porous fillers and supports known in the art.
[0056] Fatty acid salts may also be present in the polyolefln compositions.
Such salts may be present from 0.001 to 2 W% of the composition in one embodiment, and from 0.01 to 1 wt% in another embodiment. Examples of fatty acid metal salts include lauric acid, stearic acid, succinic acid, stearyl lactic acid, lactic acid, phthalic acid, benzoic acid, hydroxystearic acid, ricinoleic acid, naphthenic acid, oleic acid, palmitic acid, and erucic acid, suitable metals including Li, Na, Mg, Ca, Sr, Ba, Zn, Cd, Al, Sn, Pb and so forth. Desirable fatty acid salts are selected from magnesium stearate, calcium stearate, sodium stearate, zinc stearate, calcium oleate, zinc oleate, and magnesium oleate.
[0057] With respect to the physical process of producing the blend of polyolefin and one or more additives, sufficient mixing should take place to assure that a uniform blend will be produced prior to conversion into a finished product. The polyolefin can be in any physical fornl when used to blend with the one or more additives. In one embodiment, reactor granules, defined as the granules of polymer that are isolated from the polymerization reactor, are used to blend with the additives. The reactor granules have an average diameter of from 10 pm to 5 mm, and from 50 ~m to 10 nnn in another embodiment. Alternately, the polyolefm is in the form of pellets, such as, for example, having an average diameter of from 1 nun to 6 rmn that are fornied from melt extuusian of the reactor granules.
[0058] One method of blending the additives with the polyolefin is to contact the components in a tumbler or other physical blending means, the polyolefin being in the form of reactor granules. This can then be followed, if desired, by melt blending in an extruder. Another method of blending the components is to melt blend the polyolefin pellets with the additives directly in an extruder, Brabender or any other melt blending means.
[0059] The resultant polyolefm resin may be further processed by any suitable means such as by calendering, casting, coating, compounding, extrusion, foaming; alI forms of molding including compression molding, injection molding, blow molding, rotational molding, and transfer molding; film blowing or casting and all methods of film formation to achieve, for example, uniaxial or biaxial orientation; theunofonning, as well as by lamination, pultrusion, protmsion, draw reduction, spinbonding, melt spinning, melt blowing, and other forms of fiber and nonwoven fabric formation, and combinations thereof. These and other forms of suitable processing techniques are described in, for example, Plastics Processing (Radian Corporation, Noyes Data Corp. 1986).
[0060] In the case of injection molding of various articles, simple solid state blends of the pellets serve equally as well as pelletized melt state blends of raw polymer granules, of granules with pellets, or of pellets of the two components since the forming process includes a remelting and mixing of the raw material. In the process of compression molding of medical devices, however, little mixing of the melt components occurs, and a pelletized melt blend would be preferred over simple solid state blends of the constituent pellets and/or granules.
Those slcilled in the art will be able to determine the appropriate procedure for blending of the polymers to balance the need for intimate mixing of the component ingredients with the desire for process economy. Common rheological propeuties, processing methods and end use applications of metallocene based polyolefins are discussed in, for example, 2 Metallocene-Based Polyolefins 400-554 (John Scheirs & W. Kaminslcy, eds. John Wiley &
Sons, Ltd.
2000).
[0061] The polymers produced and blends thereof are useful in such funning operations as film, sheet, and fiber extension and co-extrusion as well as blow molding, injection molding and rotary molding. Films include blown or cast films formed by coextrusion 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, membranes, etc. in food-contact and non-food contact applications. 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, geotextiles, etc. Extruded articles include medical tubing, wire and cable coatings, pipe, geomembranes, and pond liners.
Molded articles include single and mufti-layered constructions in the form of bottles, tanks, large hollow articles, rigid food containers and toys, etc.
[0062] Other desirable articles that can be made from and/or incorporate the polymer produced herein include automotive components, sporting equipment, outdoor furniture (e.g., garden furniture) and playground equipment, boat and water craft components, and other such articles.
More particularly, automotive components include such as bmnpers, grills, trim parts, dashboards and instrument panels, exterior door and hood components, spoiler, wind screen, hub caps, miwor housing, body panel, protective side molding, and other interior and external components associated with automobiles, trucks, boats, and other vehicles.
[0063] Further useful articles and goods include crates, containers, packaging material, labware, office floor mats, instrumentation sample holders and sample windows;
liquid storage containers for medical uses such as bags, pouches, and bottles for storage and IV infusion of blood or solutions; wrapping or containing food preserved by irradiation, other medical devices including infusion kits, catheters, and respiratory therapy, as well as packaging materials for medical devices and food which may be irradiated by gamma or ultraviolet radiation including trays, as well as stored liquid, particularly water, milk, or juice, containers including unit servings and bulk storage containers.
Film Extrusion and Film Properties [0064] The polymers produced are more easily extruded into film products by cast or blown film processing teclmiques with lower motor load, higher throughput and/or reduced head pressure as compared to EXCEEDTM resins (available from ExxonMobil Chemical Co.) of comparable melt index, comonomer type and density. Such polyolefin resins have, for a comparable MI, a higher weight average molecular weight and a broader MWD than does an EXCEEDTM resin.
[0065] The improvement in tear properties of the film can be expressed as a ratio of MD to TD
tear (Elmendorf). This ratio will generally be > 0.9, or >_ 1.0, or > 1.1, or > 1.2, or >. 1.3. In another embodiment, MD tear values of > 350 g/mil, or >_ 400 g/mil, or > 450 g/mil or >, 500 g/mil are contemplated. Intrinsic tear, determined by Llslllg the same test as both MD and TD
tear, but prepared by compression molding a plaque, is generally believed to be greater than MD tear for LLDPE materials. However, the Elmendorf tear divided by intrinsic tear will be >_ 1, or >. 1.1, or > 1.2, or > 1.4, or > 1.6. In other embodiments, the dart drop impact resistance (dart) is > 500 g/mil (>_ 500 g/0.254 nnn) as measured by ASTM D-1709.
[0066] The polymers produced will exhibit a weight average molecular weight of from 25,000 to 200,000 at corresponding MI (I2, 190°C/2.16 lcg) values that range between 10 and 0.1 dg/mil, and the weight average molecular weight ranges from 80,000 to 150,000 within which range the melt index respectively ranges from a value of 3 to 0.5 dg/min. For such polyolefin resins, the melt index ratio (MIR defined by I~~/I2 described herein) is >_ 20 or < 40, and >_ 25 or < 38.
[0067] The film may have a total thiclmess ranging from >_ 0.1, or >_ 0.2, or > 0.3mils, (_> 2.5 or > 5.1 or > 7.6 microns) or <3 or < 2.5, or < 2, or < 1.5, or <_ 1, or _< 0.8, or < 0.75, or _<
0.6 mils (<_ 76 or < 64, or < 51, or < 38, or < 25, or < 20, or _< 19, or < 15 microns. Typical die gaps range from 30-120 mils, or 60-110 mils. Melt temperatures range from 176°C- 288°C
(350-550°F), or 1980-232°C (390-450°F). Draw down ratios range from 20 - 50, or around 30-40.
[0068] For a 0.75 mil film for example, tensile strength may vary from 7000 to 12000 psi, preferably from 7500 to 12000 psi, more preferably from 8000 to 11000 psi, and most preferably from S500 to 10500 psi; and Elmendorf tear in the machine direction may vary from 300 to 1000 g/mil, preferably between 350 and 900 g/mil, more preferably between 400 and S00 g/mil and most preferably bet<veen 500 and 750 g/mil.

[0069] The 1 % secant modulus as measured by ASTM D-790 is greater than 10,000 psi, greater than 15,000 psi, greater than 20,000 psi, greater than 25,000 psi, and greater than 35,000 psi. Preferably, the 1% secant modulus is greater than 20,000 psi. More preferably, the 1 % secant modulus is greater than 23,000 psi. Most preferably, the. 1 %
secant modulus is greater than 25,000 psi.
EXAMPLES
[0070] In order to provide a better understanding of the foregoing discussion, the following non-limiting examples are offered. Although the examples may be directed to specific embodiments, they are not to be viewed as limiting the invention in any specific respect.
[0071] All parts, propoutions, and percentages are by weight unless otherwise indicated. All examples were care ied out in dry, oxygen-free enviromnents and solvents. All molecular weights are weight average molecular weight unless otherwise noted. Molecular weights (weight average molecular weight (MW) and number average molecular weight (M") and (MZ) were measured by Gel Pernieation Chromatography (GPC).
Definitions and Testing Periods Melt Index (MI) ~ g/10 min. ASTM D-1238, condition E
cz 190C

Density g/cc ASTM-D-1238 Dart Drop Impact FSO G and g/mil ASTM D-1709 Elmendorf Tear G (g/mil) ASTM-D-1922 Secant Modules ( 1 Psi ASTM D-790A
, o) [0072] Melt strength was measured at 190 °C using a commercial instrument (Rheotester 1000) from Goettfert, Germany. CRYSTAF data was obtained using a commercial instrument (Model 200) from PolymerChar S.A., Valencia, Spain. Using a technique outlined in Macromol. Mater.Eng. 279, 46-51 (2000). Approximately 30 mg sample was heated to 160 °C
at 25 °C/min in 30 mL of a chlorinated aromatic solvent (ortho-dichlorobenzene or trichlarobenzene) with stirring and held for 60 min. The solution was then cooled to 100 °C at °C/min and equilibrated for 45 min. The concentration was then monitored as the sample was cooled to 30 °C at 0.2 °C/min.

Catalyst Preparation 1. Preparation of Bis(propylcyclopentadienyl)hafnium dichloride: (PrCp)2HfC12.
[0073] HfCl4 (30.00 g, 93.7 mmol, 1.00 equiv.) was added to ether (400 mL) at -35°C and stiiTed to give a white suspension. The suspension was recooled to -35°C and then lithium propylcyclopentadienide (21.38 g, 187 nnnol, 2.00 equiv.) was added in portions. The reaction turned light brown and became thick with suspended solid on adding the lithium propylcyclopentadienide. The reaction was allowed to warm slowly to room temperature and stiiTed 17 hours. The brown mixture was filtered to give brown solid and a straw yellow solution. The solid was washed with ether (3 x 50 mL) and the combined ether solutions were concentrated to 100 mL under vacuum to give a cold, white suspension. Off white solid was isolated by filtration and dried under vacuum. Yield 33.59 g (77%). IH
NMR(CD2Cl2): 8 0.92 (t, 6H, CHZCH2CH3), 1.56 (m, 4H, CHZCH2CH~), 2.60 (t, 4H, CH~CHyCH3), 6.10 (m, 4H, Cp-H), 6.21 (m, 4H, Cp-H).
2. Preparation of Bis(propylcyclopentadienyl)hafnium difluoride: (PrCp)ZHfF2.
[0074] To a murky green-brown solution of bis(propylcyclopentadienyl)hafnium dichloride (70.00 g, 151 rnmol, 1.00 equiv.) in dichloromethane (350 mL) was added tributyltin fluoride (98.00 g, 317 rnmol, 2.10 equiv.). The reaction was lighter amber after stirring 10 min. The reaction was stirred 130 minutes and then filtered through celite to give an amber solution and off white solid. The solid was washed with dichloromethane and the combined dichloromethane solution was evaporated under vacuum, leaving a soupy manila mixture.
Pentane (1 L) was added to the mixture, wluch was stirred 10 minutes and cooled to -35°C.
The resulting off white solid was filtered and washed with cold pentane (3 x 75 mL) and dried under vacuum to give a white powder. Yield 56.02 g (86%). 1H NMR(CD~CI~): 8 0.92 (t, 6H, CH~CH2CH~), 1.55 (m, 4H, CH~CH~CH3), 2.47 (t, 4H, CH~CH2CH~), 6.00 (m, 4H, Cp-H), 6.23 (m, 4H, Cp-H). 19F NMR(CD~C12): 8 23.9.
Preparation of Active Catalyst [0075] The active catalysts were made at a Al/Hf mole ratio of 120:1 and the hafnium loading on the finished catalyst was 0.685 wt% Hf using the following general procedure.
Methylaluminoxane (MAO) 1140 cc of a 30 wt% solution in toluene (obtained from Albemarle Corporation, Baton Rouge, Louisiana) was added to a clean, dry 2 gallon vessel and stirred at 60 rpm and 80°F for 5-15 min. An additional 1500-1800 cc of toluene was added while stirring. The metallocene was dissolved in 250 cc toluene and the transfer vessel was rinsed with an additional 150 cc of toluene. The metallocene/MAO mixture was stirred at 120 rpm for 1 how. Next, 850 g of silica, Ineos 757 (Ineos Silicas Limited, Warrington, England, dehydrated at 600°C) was added and stirred for 55 min. The catalyst was then dried at 155°F
for 10 hours under flowing nitrogen while being stirred at 30 rpm.
[0076] The metallocene for Example 1 was bis(n-propylcyclopentadienyl) hafnium dichloride (21.6 g). The metallocene for Examples 2-6, 12-13 and Comparative Example 14 was bis(n-propylcyclopentadienyl) hafnium difluoride. The catalyst for Example 7 was prepared in a similar manner except that bis(n-propylcyclopentadienyl) hafnium dichloride was used and the silica was Davison 948 (W.R. Grace, Davison Chemical Division, Baltimore, Maryland, dehydrated at 600°C). The metallocene for Comparative Example 11 was bis(n-propylcyclopentadienyl) hafnium dichloride.
Polymer Production [0077] Using the catalyst systems described above, ethylene/1-hexene copolymer was produced according to the reaction conditions listed in Table 1.

d- M ~ N 'O. ~n O

~n N O oo ~n ~

_ O

M ~n O V~ l~

--~ ,-w 0 N O I~ d~

'-' d- N O

N vo 01 V7 I~

~n N n I~ d-~

_ ~ N O N

.-~ oo ~,-~

~ ~ M N O o0 d-M N

: 1 V O
O '1 d l~ ~ N N O l~ d--, d' Q

_ ~ N O 00 ' ,_, vo M N N o 0o N

c~

W O

N ~ ~n c M N ~ ~ N
n (V

W , cat O

~

_ O t~ O

O l~
N

d- N N O n M

M

M M M N O l~ M

N

n r, O

_ N 01 O 'd ~ O

N M M N O o0 N

W o ~

01 ~ ' O V
d N M N O t~ ~t c~

O

"C

~
O

U

o _~

V ~ ~-' N ~'1 r O ' ~ c~C ~
~

p .. _ rte " o ~ N ., H

b 'o r~., U

E~ W 0.~ ~ U U H

[0078] The ethylene/1-hexene copolymers from Examples 1-6 were produced in accordance with the following general procedure. Polymerization was conducted in a 14 inch diameter gas-phase fluidized bed reactor operating at approximately 350 psig total pressure. The reactor bed weight was approximately 100 pounds. Fluidizing gas was passed through the bed at a velocity of approximately 2.0 feet per second. The fluidizing gas exiting the bed entered a resin disengaging zone located at the upper portion of the reactor. The fluidizing gas then entered a recycle loop and passed through a cycle gas compressor and water-cooled heat exchanger. The shell side water temperature was adjusted to maintain the reaction temperature to the specified value. Ethylene, hydrogen, 1-hexene and nitrogen were fed to the cycle gas loop just upstream of the compressor at quantities sufficient to maintain the desired gas concentrations. Gas concentrations were measured by an on-line vapor fraction analyzer. The catalyst was fed dry or as a mineral oil slurry (17 wt% solids) to the reactor bed through a stainless steel injection tube at a rate sufficient to maintain the desired polymer production rate.
Nitrogen gas was used to disperse the catalyst into the reactor. Product was withdrawn from the reactor in batch mode into a purging vessel before it was transfeiTed into a product drum.
Residual catalyst and cocatalyst in the resin was deactivated in the product drum with a wet nitrogen purge.
[0079] The ethylene/1-hexene copolymers from Examples 7, 12, and 13 and Comparative Example 14 were produced in accordance with the following general procedure.
Polymerization was conducted in a 24 inch diameter gas-phase fluidized bed reactor operating at approximately 300 psig total pressure. The reactor bed weight was approximately 600 - 700 pounds. Fluidizing gas was passed through the bed at a velocity of approximately 2.25 feet per second. The fluidizing gas exiting the bed entered a resin disengaging zone located at the upper portion of the reactor. The fluidizing gas then entered a recycle loop and passed through a water-cooled heat exchanger and cycle gas compressor. The shell side water temperature was adjusted to maintain the reaction temperature to the specified value.
Ethylene, hydrogen, 1-hexene and nitrogen were fed to the cycle gas loop just upstream of the compressor at quantities sufficient to maintain the desired gas concentrations. Gas concentrations were measured by an on-line vapor fraction analyzer. The catalyst was fed to the reactor bed through a stainless steel injection tube at a rate sufficient to maintain the desired polymer production rate. Nitrogen gas was used to disperse the catalyst into the reactor. Product was withdrawn from the reactor in batch mode into a purging vessel before it was transferred into a product ''4 -drum. Residual catalyst and cocatalyst in the resin was deactivated in the product drum with a wet nitrogen purge.
[0080] Granular product for Examples 1-7 was screened and dry-blended with 500 ppm IrganoxC~ (IR) (available from Ciba-Geigy) 1076, 2000 ppm IR168 and 800 ppm Dynamar Fx5920A (processing aid from Dyneon) using a double-cone blender. Pelleting of Examples 1 through 6 was carried out on a Werner 8c Pfleiderer ZSh 57-mm twin-screw extruder equipped with an underwater pelletizer. Output rate was approximately 175-185 lb/hr and melt temperature was 231 °C (447°F). Example 7 was pelletized on a Farrel continuous mixer at an output rate of 500 lb/h with a specific energy input of 0.125 hp-hr/lb a.nd a melt temperature of 219°C. Granular product for Examples 12-13 and Comparative Example 14 was screened and dry-blended with 1500 ppm IR 1076, 1500 ppn IR 168 and 900 ppm zinc oxide.
Pelleting was carried out on a Wemer & Pfleiderer ZSK 57-mm twin-screw extruder equipped with an underwater pelletizer. Output rate was approximately 200 lb/hr and melt temperature was 214-218°C.
Blown Film Production [0081] Blown films were extnided on a 2.5" Battenfield Gloucester' line (30:1 L:D) equipped with a 6" oscillating die. Output rate was 188 lb/hr (10 lb/hr/in die circumference) and the die gap was 60 mil. The target film gauge was 0.75 mil and BUR was held constant at 2.5. FLH
was typically 19-24". A standard "hump" temperature profile was used where "BZ" is barrel zone: BZ1=310 / BZ2=410 / BZ3=375 / BZ4=335 / BZS=335 / Adapter=390 /
Die=390°F.
[0082] Cast films were extended on a 3.5" Black Clawson line (30:1 L:D) equipped with a 42"
slot die. Line speed was set at 750 ft/min and output was adjusted (typically 575-590 lb/h) to achieve a 0.8 mil film. A standard "hump" temperature profile was used where "BZ" is barrel zone: BZ1=350 / BZ2=450 / BZ3=525 / BZ4=540 / BZS=540 / BZ6=530 /
Die=550°F. The film edge was trirmned to give a 20" roll for testing.
[0083] Comparative Example 8 is NTX-095, a commercially available Super Strength or super hexene Z-N LLDPE from ExxonMobil Chemical Company. Comparative Example 9 is EXCEED~ 1018CA, a corrunercially available mLLDPE from ExxonMobil Chemical Company. Comparative Example 10 is Escorene~ LL3001.63, a commercially available Z-N LLDPE from ExxonMobil Chemical Company. Comparative Example 15 is E~CEED~
3518CB, a conmlercially available mLLDPE from ExxonMobil Chemical Company.

_ 25 _ Comparative Example 16 is EXCEED~ 2718CB, a commercially available mLLDPE from ExxonMobil Chemical Company. Comparative Example 17 is Escorene~ LL3002.32, a commercially available Z-N LLDPE from ExxonMobil Chemical Company.
Film Properties [0084] The blown film propeuties and extrusion data are shown in Table II.
Cast film properties and extrusion data are shown in Table III.

Table II: Blown Film Properties for Examples 1-7:
Exam le 1 2 3 ~ 4 5 6 7 0 0 0 0.95 O.S7 0.97 0.65 MI (IZ) d /min . . .

25 9 24 29.2 26 24.3 15.9 HLMI (I2,) d . . . .
/min 3 24 32 30.7 30.7 25.1 29.1 MIR (IZ,/h) . . .

3 3.24 3.58 3.33 3.68 31.3 2.81 MW~ .

2 2 2.66 2.66 2.71 2.29 2.38 MAW . .

25.5 30 23.7 33.5 22.7 32.8 21.7 CDBI (%) .

21 15 20 20.5 20.9 18.7 22.0 SDBI (C) . . .

5 4.5 5.6 5.2 5.3 4.3 ~6.4 Melt Stren th .
(cN) 26 35 26 38.0 31 30 Veloci (fmal/initial) .

0.91850.9195 0.9164 0.9209 0.91 0.9176 0.9195 Resin Density (alec) Tensile @ Yield1390 1400 1320 1480 1390 1300 1440 MD

( si) Tensile @ Yield1510 1460 1390 1630 1500 1340 N/a TD

( si) Tensile @ Break10450 9270 10220 9530 9400 97S0 10400 MD

( si) Tensile ~ Break6400 7090 71 SO 7160 7490 7510 N/a TD

( si) Elongation @ 290 350 290 330 320 360 300 Break MD (%) Elongation L 610 620 620 650 630 610 N/a Break TD (%) 1% Secant Modulus27370 26310 24150 28990 26330 22450 30470 MD ( si) 1,~o Secant 35110 31920 30610 35460 33590 26690 35910 Modulus TD ( si) Elmendorf Tear 640 550 610 710 610 390 760 MD

( /mil) ElmendorFTear 620 540 540 550 560 510 650 TD

( /mil) 1.03 1.02 1.13 1.29 1.09 0.76 1.17 MD/TD

Dart Im act ( /mil) 0 0 0.73 0.73 0.74 0.74 0.73 Gau a Mic (mils). .

Shrink MD (%) -27 -20 -24 -21 -23 -19 ~6 Shrink TD (%) Extrusion Parameters:

Melt Tem erature (C) Head Pressure ( si) Die Pressure ( si) 62.4 65.5 64.1 62.5 63 .1 63.6 69.9 Motor Load (am s) Table II (continued): Blomn Flhll Properties for Comparative Examples 8-11.
Exam le 8 9 10 11 MI (Iz) (d /min)1.00 0.96 1.01 1.0 HLMI (h,) (d 25.5 15.6 31.3 23.5 /min) MIR (I~i/I2) 25.5 16.3 31.0 23.5 3.51 2.34 3.91 3.28 ~4w~

2.85 1.9 3.25 2.24 Mz/Mw 21.2 64.7 22.4 40.3 CDBI (%) 21.9 11.6 22.0 17.3 SDBI (C) 'l~6 3.7 N/a N/a Melt Strength (cN) 36 27 N/a N/a Veloci (final/initial O 0 0.9174 0.9167 Resin Densi (a/cc). .

Tensile @ Yield 1250 1350 1310 1244 MD

( si) Tensile @ Yield 1310 1390 1400 1265 TD

( si) Tensile @ Break 8240 10310 9330 7782 MD

( si) Tensile @ Break 5570 6920 6560 9755 TD

( si) Elongation @ 500 440 430 424 Break MD

(%) Elongation @ 670 580 760 624 Break TD

(%) 1% Secant Modulus22620 24250 27800 26400 MD

( si) 1 % Secant Modulus24780 27650 33680 32100 TD

(psi) Elmendorf Tear 440 290 420 23S
MD

( /mil) Ehnendorf Tear 760 510 860 495 TD

( /mil) 0.58 0.57 0.49 0.48 MD/TD

Dart Im act (g/mil) 0.84 0.73 0.75 1.00 Gau a Mic (mils) 64 58 70 N/a Shrink MD (%) -15 -12 -21 N/a Shrink TD (i) Extrusion:

430 401 393 N/a Melt Tem . (C) Head Pressure ( si) _ 2260 2490 2290 N/a Die Pressure ( si) 62.5 71.3 64.4 68.6 Motor Load (am s) -~s-Table III: Cast Film Properties Examples; 12 13 14 15 16 17 MI (I~) (dg/mui)2.65 3.26 3.75 3.52 2.76 1.87 HLMI (I~,) (dg/min)76.8 97.3 81.7 58.4 43.9 55.6 MIR (h,/h) 28.7 29.8 21.6 16.6 15.9 29.7 Mw/Mn 3.21 3.43 3.20 2.45 2.52 4.40 Mz/M~~~ 2.40 2.46 3.17 1.81 1.74 2.95 CDBI (%) 28.3 28.5 49.9 73.8 70.4 21.3 SDBI (C) 30.1 20.1 16.3 12.7 12.7 22.2 Resin Density 0.9186 0.9201 0.9303 0.9199 0.9201 0.919 (g/cc) Tensile @ Yield MD

(psi) Tensile @ Yield TD

(psi) 730 750 710 670 730 830 Tensile @ Break MD

(psi) 7670 6980 7190 7690 7430 7830 Tensile @ Break TD

(psi) Elongation @
Break MD (%) Elongation @
Break TD (%) 730 720 680 690 680 850 1% Secant Modulus MD (psi) 1% Secant Modulus TD

(psi) Elmendorf Tear MD

(g/mil) 390 380 270 210 220 350 Elmendorf Tear TD

(g/mil) 520 490 510 490 450 930 MD/TD 0.75 0.78 0.53 0.43 0.49 0.38 Dart Impact 190 160 160 180 260 100 (g/mil) Gauge Mic (mils)0.80 0.79 0.76 0.78 0.80 0.81 Table III (continued):
Extrusion Parameters:

Melt Temperature553 548 548 562 575 564 (C) Head Pressure 3500 3670 3880 4310 4630 4050 (psi) Die Pressure 1060 970 920 1010 1190 1300 (psi) Motor Load (amps)192 190 193 231 241 305 [0085] As shown in the Tables above, lower reactor temperatures surprisingly broadened the comonomer distribution as evidenced by a decrease in the composition distribution breadth index (CDBI) and an increase in the solubility distribution breadth index (SDBI). Furthermore, lower polymerization temperatures or increased ethylene partial pressures or both surprisingly broadened molecular weight distribution, as evidenced by an increase in Mw/Mn and Mz/Mw.
Accordingly, a polyolefin film was produced having a high machine direction tear (MD tear), a high transverse direction tear (TD tear), a high 1% secant modulus, and a high dart drop impact resistance (dart).
[0086] Unless otherwise indicated, all numbers expressing quantities of ingredients, properties, reaction conditions, and so forth, used in the specification and claims are to be understood as approximations based on the desired properties sought to be obtained by the present invention, and the ewor of measurement, etc., and should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.
Notwithstanding that the nwnerical ranges and values setting forth the broad scope of the invention are approximations, the numerical values set forth are reported as precisely as possible.
[0087] All priority documents are herein fully incorporated by reference for all jurisdictions in which such incorporation is permitted. Further, all documents cited herein, including testing procedures, are herein fully incorporated by reference for all jurisdictions in which such incorporation is permitted.
[0088] While the foregoing is directed to embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof and the scope thereof is deterniined by the claims that follow.

Claims (10)

1. ~A method for producing a polyethylene film, comprising:
reacting ethylene and a comonomer in the presence of a hafnium-based metallocene at a temperature of from 70°C and 90°C, an ethylene partial pressure of from 120 psia and 260 psia, and a comonomer to ethylene mole ratio of from 0.01 to 0.02 to produce an ethylene based polymer; and extruding the ethylene based polymer at conditions sufficient to produce a polyethylene film comprising a 1% secant modulus of greater than 25,000 psi, a dart impact resistance of greater than 500 g/mil, and a MD tear strength of greater than g/mil.

2. ~The method of claim 1, wherein the hafnium-based metallocene is represented by the following formula:
Cp A C p B HfX2 wherein each X is independently selected from the group consisting of fluorine, chlorine, iodine, bromine, and combinations thereof; and Cp A and Cp B are bound to the Hf, and are independently selected from the from the group consisting of cyclopentadienyl, indenyl, tetrahydroindenyl, fluorenyl, substituted derivatives thereof and a combination thereof.

3. ~The method of any of the preceding claims, wherein the hafnium-based metallocene is bis(propylcyclopentadienyl) hafnium dichloride or bis(propylcyclopentadienyl) hafnium difluoride.

4. ~The method of any of the preceding claims, wherein the temperature is from 75°C to 80°C.

5. ~The method of any of the preceding claims, wherein the ethylene partial pressure is from 220 psia to 260 psia.

6. The method of any of the preceding claims, wherein the comonomer is 1-hexene.

7. The method of any of the preceding claims, wherein the ethylene based polymer has a Composition Distribution Breadth Index (CDBI) of from 20% to 50% and a Solubility Distribution Breadth Index (SDBI) of from 18°C to 22°C.

8. The method of any of the preceding claims, wherein the ethylene based polymer has a Composition Distribution Breadth Index (CDBI) of from 20% to 35% and a Solubility Distribution Breadth Index (SDBI) of from 18.7°C to 21.4°C.

9. The method of any of the preceding claims, wherein the ethylene based polymer has a ratio of Z-average molecular weight to weight average molecular weight of from 2.2 to 3.

10. The method of any of the preceding claims, wherein extending comprises blown film extrusion or cast film extrusion.