CA2824482C

Method for preparing monocyclopentadienyl compounds

Abstract

A method for preparing a monocyclopentadienyl compound comprises refluxing for about 20 hours a dicyclopentadienyl compound and a metal tetrachloride, providing the monocyclopentadienyl compound in at least about 70% yield.

CA2824482C, drawing sheet 1 — Sheet 1 of 35

Term

Term ended

Expired 18 August 2026, 0.1 years ago.

4 claims: 1 independent, 3 dependent

1
CA 02824482 2015-09-23 What is claimed is:1. A method of preparing a monocyclopentadienyl compound having the formula (1,3 R2R4Cp)MCl3, comprising: refluxing for substantially 20 hours in a solvent comprising (a) a metal tetrachloride compound: and (b) a compound having the formula (1,3 R2R4Cp)2MCl2;and providing the monocyclopentadienyl compound in at least 70% yield;wherein M is Zr of Hf;wherein R2 is H, an alkyl group, or an alkenyl group;and wherein R4 is H, an alkyl group, or an alkenyl group.

412 paragraphs in 51 sections, as filed

CA 02824482 2015-01-26

METHOD FOR PEPARING MONOCYCLOPENTADIENYL COMPOUNDS

This application is a divisional application of Canadian Patent File No. 2,621,475 filed August 18, 2006 from PCT/US2006/032542.

TECHNICAL FIELD OF THE INVENTION

This invention relates to the field of olefin polymerization catalysis, catalyst compositions, methods for the polymerization and copolymerization of olefins, polyolefins, and film and pipe resins formed therefrom, particularly using a supported catalyst composition. The present invention also relates to the fields of organic synthesis and organometallic synthesis, including synthetic methods for half10 metallocenes.

BACKGROUND OF THE INVENTION

Presently, a variety of polyethylene (PE) resins can be used to produce high stiffness pipe used in water, gas, and other fluid transport applications. Polyethylene pipe classified as PE-100, MRS 10, or ASTM D335O typical cell classification 345566C is especially desirable for use under conditions requiring higher pressure ratings. To obtain a PE-100 classification, PE-100, pipe is required to meet certain standards specifying stiffness,, resistance to slow crack growth, resistance to chemical attack, and low-temperature toughness (expressed as rapid crack propagation). Further, such pipe must meet a deformation standard that is determined under pressure at elevated temperatures. It is also desirable for PE-100 pipe to exhibit toughness, for example, where the pipe is buried underground or where the pipe is used to transport coarse or abrasive slurries. Accordingly, there is a need for a resin and a PE-100 pipe made therefrom that has improved physical 25 properties and impact resistance properties.

With conventional processes and resins formed using metallocene catalyst systems, there is a trade off between high stiffness and high environmental stress cracking resistance (ESCR). While either high stiffness or high ESCR items can be manufactured, conventional processes do not produce items having both high 30 stiffness and high ESCR.

CA 02824482 2015-09-23

SUMMARY OF THE INVENTION

The present invention generally relates to a catalyst composition including two metallocene compounds, an activator, and a cocatalyst. The present invention further relates to processes for producing such a catalyst composition, polymerization processes, and polymers produced therefrom. The metallocene compounds are combined with an activator, an aluminum alkyl compound, and olefin monomers to produce a polyolefin having a bimodal molecular weight distribution. The resulting polymers feature an outstanding balance of stiffness and slow crack growth resistance. Additionally, the polymers produced according to the present invention have excellent strength.

Although the invention as disclosed is noted above, and is further described herein, the invention as set forth in this divisional application pertains to a method of preparing a monocyclopentadienyl compound having the formula (1,3 R2R4Cp)MCl3, comprising refluxing for substantially 20 hours in a solvent comprising: (a) a metal tetrachloride compound, and (b) a compound having the formula (1,3 R2R4Cp)2MCl2; and providing the monocyclopentadienyl compound in at least 70% yield; wherein M is Zr of Hf; wherein R2 is H, an alkyl group, or an alkenyl group; and wherein R4 is H, an alkyl group, or an alkenyl group.

In accordance with the invention as disclosed, the two metallocene compounds are selected such that the polymers produced therefrom have distinctly different molecular weights. One of the metallocenes, typically a tightly bridged metallocene containing a substituent that includes a terminal olefin, produces a high molecular weight component. Another metallocene, which typically is not bridged and often is more responsive to hydrogen than the first metallocene, produces a low molecular weight component of the resin.

CA 02824482 2015-09-23

According to one aspect of the present invention, a catalyst composition comprises a first metallocene compound, a second metallocene compound, an activator-support, and an organoaluminum compound. The first metallocene compound has the formula:

(X')(X2R12)(X3)(X4)M1;

wherein (X1) is cyclopentadienyl, indenyl, or fluorenyl, (X2) is fluorenyl, and (X1) and (X2) are connected by a disubstituted bridging group comprising one atom bonded to both (X1) and (X2), wherein the atom is carbon or silicon. A first substituent of the disubstituted bridging group is an aliphatic or aromatic group having from 1 to about 20 carbon atoms. A second substituent of the disubstituted bridging group is a saturated or unsaturated aliphatic group having from 3 to about 10 carbon atoms. R1 is H or an alkyl group having from 1 to about 4 carbon atoms, (X3) and (X4) independently are halide, and M1 is Zr or Hf. The first substituent of

CA 02824482 2013-08-22 the disubstituted bridging group may be phenyl or methyl. The second substituent of the disubstituted bridging group may be butenyl, pentenyl, or hexenyl.

According to this and other aspects of the present invention, the first metallocene may be:

CA 02824482 2013-08-22

CA 02824482 2013-08-22

wherein R2 is H or -CH3; R3 is CHf^CHCHr, CH2=CH(CH2)2-, Ph(CH2)3-, CH3(CH2)3, or H; X5 and X6 independently are a halide; and M2 is Zr or Hf.

According to this and other aspects of the present invention, the ratio of the first metallocene compound to the second metallocene compound may be from about 1:10 to about 10:1. According to other aspects of the present invention, the ratio of the first metallocene compound to the second metallocene compound may be from about 1:5 to about 5:1. According to yet other aspects of the present invention, the ratio of the first metallocene compound to the second metallocene compound maybe from about 1:2 to about 2:1.

The organoaluminum compound used with the present invention may have the formula:

(R2)3A1;

wherein (R2) is an aliphatic group having from 2 to about 6 carbon atoms. In some instances, (R2) is an ethyl group, a propyl group, a butyl group, a hexyl group, or an isobutyl group.

According to another aspect of the present invention, a catalyst composition comprises an onsa-metallocene compound, an uribridged metallocene compound, an activator-support, and an organoaluminum compound. The ansa-metallocene compound is:

CA 02824482 2013-08-22

The unbridged metallocene compound is:

a combination therof.

. According to this and other aspects of the present invention, the activatorsupport may be fluorided alumina, chlorided alumina, bromided alumina, sulfated alumina, fluorided silica-alumina, chlorided silica-alumina, bromided silica-alumina, sulfated silica-alumina, fluorided silica-zirconia, chlorided silica-zirconia, bromided 10 silica-zirconia, sulfated silica-zirconia, a pillared clay, or any combination thereof.

The catalyst composition of the present invention may thus comprise a first .metallocene compound, a second metallocene compound, an activator-support, and at least one organoaluminum compound, wherein:

(a) the first metallocene compound is:

CA 02824482 2013-08-22 (b) the second metallocene compound is:

ch2ch=ch2 .

(d) the organoaluminum compound is tri-n-butylaluminum.

The present invention also contemplates a process for polymerizing olefins in the presence of a catalyst composition. The process comprises contacting die catalyst composition with at least one type of olefin monomer under polymerization conditions, where the catalyst composition comprises an OHSc-metallocene compound, an unbridged metallocene compound, an activator-support, and an organoaluminum compound. The ansa-metallocene compound has the formula:

(X’jÇX^ÇX’^M1;

wherein (X1) is cyclopentadienyl, indenyl, or fluorenyl, (X2) is fluorenyl, and (X1) and (X2) are connected by a disubstituted bridging group comprising one atom bonded to both (X1) and (X2), wherein the atom is carbon or silicon. A first substituent of the disubstituted bridging group is an aliphatic or aromatic group having from 1 to about 20 carbon atoms. A second substituent of the disubstituted bridging group is a saturated or unsaturated aliphatic group having from 3 to about 10 carbon atoms. Rl is H or an alkyl group having from 1 to about 4 carbon atoms, (X3) and (X4) independently are a halide, and M1 is Zr or Hf.

The uhbridged metallocene has the formula:

CA 02824482 2013-08-22

wherein R2 is H or -CH3; R3 is CH2«CHCH2-, Ph(CH2)3-,

CH3(CH2)3, or H; X5 and X6 independently are a halide; and M2 is Zr or Hf.

The present invention further contemplates a process for producing a catalyst 5 composition comprising contacting a first metallocene compound, a second metallocene compound, an activator-support, and at least one organoalununum compound. The first metallocene compound has the formula:

(X’XX’R’iXX’XX*^ wherein (X1) is cyclopentadienyl, indenyl, or fluorenyl, (X2) is fluorenyl, and (X1) 10 and (X2) are connected by a disubstituted bridging group comprising one atom . bonded to both (X1) and (X2), wherein the atom is carbon of silicon. A first substituent of the disubstituted bridging group comprises an aliphatic or aromatic group having from 1 to about 10 carbon atoms. A second substituent of the disubstituted bridging group is a saturated or unsaturated aliphatic group having 15 from 3 to about 10 carbon atoms. R1 is H or an alkyl group having from 1 to about 4 carbon atoms, (X3) and (X4) independently are a halide, and M1 is Zr or Hf.

The second metallocene has the formula:

CA 02824482 2013-08-22 wherein R2 is H or -CH3; R3 is CH2=CHCH2-, CH2=CH(CH2)2-, Ph(CH2)3-,

CH3(CH2)3, or H; X5 and X6 independently are a halide; and M2 is Zr or Hf,

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 represents the NMR spectrum for the Zr^-CjH4-(nBu)]Cl3 formed according to Example 1.

FIG. 2 represents the NMR spectrum for the Zr[q-C5H4-(nBu)]Cl3 formed according to Example 2.

FIG. 3 represents a comparison of the level of monomer incorporation using 10 metallocene compounds of the present invention with that of bis-indenyl zirconium dichloride.

FIG. 4 represents the molecular weight distribution of an exemplary polymer prepared according to this invention.

DEFINITIONS

To define more clearly the terms used herein, the following definitions are provided. To the extent that any definition or usage provided by any document incorporated herein by reference conflicts with the definition or usage provided herein, the definition or usage provided herein controls.

The term “polymer” is used herein to mean homopolymers comprising ethylene and copolymers of ethylene and another olefinic comonomer. “Polymer” is also used herein to mean homopolymers and copolymers of any other polymerizable monomer disclosed herein.

The term “cocatalyst” is used generally herein to refer to the 25 organoalummum compounds that may constitute one component of the catalyst composition. Additionally, “cocatalyst” refers to the optional components of the catalyst composition including, but not limited to, aluminoxanes, organoboron compounds, organozinc compounds, or ionizing ionic compounds, as disclosed herein. The term “cocatalyst” may be used regardless of the actual function of the 30 compound or any chemical mechanism by which the compound may operate. In one

CA 02824482 2013-08-22 aspect of this invention, the term “cocatalyst” is used to distinguish that component of the catalyst composition from the metallocene compound.

The term “fluoroorgano boron compound” is used herein with its ordinary meaning to refer to neutral compounds of the form BY3. The term “fluoroorgano borate compound” also has its usual meaning to refer to the monoanionic salts of a fluoroorgano boron compound of the form [cation)+[BY4]·, where Y represents a fluorinated organic group. For convenience, fluoroorgano boron and fluoroorgano borate compounds are typically referred to collectively by “organoboron compounds”, or by either name as the context requires.

The term “precontacted” mixture is used herein to describe a first mixture of catalyst components that are contacted for a first period of time prior to die first mixture being used to form a “postcontacted” or second mixture of catalyst components that are contacted for a second period of time. Typically, the precontacted mixture describes a mixture of metallocene compound (or compounds), olefin monomer, and organoaluminum compound (or compounds), before this mixture is contacted with the activator-support and optional additional organoaluminum compound. Thus, precontacted describes components that are used to contact each other, but prior to contacting the components in the second, postcontacted mixture. Accordingly, this invention may occasionally distinguish between a component used to prepare the precontacted mixture and that component after the mixture has been prepared. For example, according to this description, it is possible for the precontacted organoaluminum compound, once it is contacted with the metallocene and the. olefin monomer, to have reacted to form at least one different chemical compound, formulation, or structure from the distinct organoaluminum compound used to prepare the precontacted mixture. In this case, the precontacted organoaluminum compound or component is described as comprising an organoaluminum compound that was used to prepare the precontacted mixture.

Similarly, the term “postcontacted” mixture is used herein to describe a second mixture of catalyst components that are contacted for a second period of time, and one constituent of which is the ‘'precontacted” or first mixture of catalyst

CA 02824482 2013-08-22 components that were contacted for a first period of time. Typically, the term postcontacted” mixture is used herein to describe the mixture of the metallocene compound, olefin monomer, organoaluminum compound, and chemically-treated solid oxide, formed from contacting the precontacted mixture of a portion of these components with any additional components added to make up the postcontacted mixture. Generally, the additional component added to make up the postcontacted mixture is the chemically-treated solid oxide, and, optionally, may include an organoaluminum compound the same or different from the organoaluminum compound used to prepare the precontacted mixture, as described herein. Accordingly, this invention may also occasionally distinguish between a component used to prepare the postcontacted mixture and that component after the mixture has been prepared.

The term “metallocene”, as used herein, describes a compound comprising two r]5-cycloalkadienyl-type ligands in the molecule. Thus, the metallocenes of this invention are bis(T]S-cyclopentadienyl-type ligand) compounds, wherein the η5cycloalkadienyl portions include cyclopentadienyl ligands, indenyl ligands, fluorenyl ligands, and the like, including partially saturated or substituted derivatives or analogs of any of these. Possible substituents on these ligands include hydrogen, therefore the description “substituted derivatives thereof’ in this invention comprises partially saturated ligands such as tetrahydroindenyl, tetrahydrofluorenyl, octahydrofluorenyl, partially saturated indenyl, partially saturated fluorenyl, substituted partially saturated indenyl, substituted partially saturated fluorenyl, and the like. In some contexts, the metallocene is referred to simply as the “catalyst”, in much the same way the term “cocatalyst” is used herein to refer to the organoaluminum compound. Unless otherwise specified, the following abbreviations are used*. Cp for cyclopentadienyl; Ind for indenyl; and Flu for fluorenyl.

The terms “catalyst composition”, “catalyst mixture”, and the like do not depend upon the actual product resulting from the contact or reaction of the components of the mixtures, the nature of the active catalytic site, or the fate of the aluminum cocatalyst, the metallocene compound, any olefin monomer used to

CA 02824482 2015-01-26 prepare a precontacted mixture, or the chemically-treated solid oxide after combining these components. Therefore, the terms “catalyst composition”, “catalyst mixture”, and the like may include both heterogeneous compositions and homogenous compositions.

The term “hydrocarbyl” is used herein to specify a hydrocarbon radical group that includes, but is not limited to aryl, allcyl, cycloalkyl, alkenyl, cycloalkenyl, cycloalkadienyl, alkynyl, aralkyl, aralkenyl, arallcynyl, and the like, and includes all substituted, unsubstituted, branched, linear, heteroatom substituted derivatives thereof.

The terms “chemically-treated solid oxide”, “solid oxide activator-support’!, “acidic activator-support”, “activator-support, “treated solid oxide compound”, or simply “activator”, and the like are used herein to indicate a solid, inorganic oxide of relatively high porosity, which exhibits Lewis acidic or Bronsted acidic behavior, and which has been treated with an electron-withdrawing component, typically an anion, and which is calcined. The electron-withdrawing component is typically an electron-withdrawing anion source compound. Thus, the chemically-treated solid oxide compound comprises the calcined contact product of at least one solid oxide compound with at least one electron-withdrawing anion source compound. Typically, the chemically-treated solid oxide comprises at least one ionizing, acidic solid oxide compound. The terms “support” and “activator-support are not used to imply these components are inert, and such components should not be construed as f .

an inert component of the catalyst composition.

Although any methods, devices, and materials similar or equivalent to those described herein can be used in the practice or testing of the invention, the typical 25 methods, devices and materials are herein described.

The publications discussed above and throughout the text are provided solely for their disclosure prior to the filing date

CA 02824482 2013-08-22 of the present application. Nothing herein is to be construed as an admission that the inventors are not entitled to antedate such disclosure by virtue of prior invention.

For any particular compound disclosed herein, any general structure presented also encompasses all conformational isomers, regioisomers, and stereoisomers that may arise from a particular set of substituents. The general structure also encompasses all enantiomers, diastereomers, and other optical isomers whether in enantiomeric or racemic forms, as well as mixtures of stereoisomers, as the context requires.

DETAILED DESCRIPTION OF THE INVENTION

The present invention is directed generally to new catalyst compositions, methods for preparing catalyst compositions, and methods for using the catalyst compositions to polymerize olefins. The present invention further is directed to a method of preparing cyclopentadienyl complexes and a method of isolating such compounds as a solid.

In particular, the present invention relates to new catalyst compositions and methods of using such catalyst compositions to form polyolefins having an excellent balance of stiffness and slow crack growth resistance. The catalyst composition includes at least two metallocenes. The first metallocene compound is used to produce a high molecular weight component, and is generally a tightly bridged metallocene containing a substituent that includes a terminal olefin. The second metallocene, used to produce the low molecular weight component, is generally not bridged and is more responsive to hydrogen than the first metallocene. The metallocenes are combined with a solid activator, an aluminum alkyl compound, and an olefin monomer to produce the desired bimodal polyolefin. It has been discovered that the bi-metallocene catalyst system of the present invention provides a useful combination of polyolefin properties, such as stiffness and slow crack growth resistance, so the resin is suitable for blowing film, forming a pipe, and so forth.

According to one aspect of the present invention, a composition of matter is provided. The composition includes a first metallocene compound, a second

CA 02824482 2013-08-22 metallocene compound, an activator-support, and an organoaluminum compound. According to other aspects, the present invention is directed to a catalyst composition, a catalyst composition for polymerizing olefins, a method of preparing a catalyst composition, a method of using a catalyst composition, and the like, in each case encompassing a first metallocene compound, a second metallocene compound, an activator-support, and an organoaluminum compound. The present invention is directed further to a method for producing polyolefins and films, and. polyolefins and film produced therefrom. According to still another aspect, the present invention is directed to a method of preparing monocyclopentadienyl compounds that may be used to form metallocene compounds.

A. Catalyst Composition and Components

The present invention is directed to a catalyst composition including a first metallocene compound, a second metallocene compound, an activator-support, and an organoaluminum compound. The first metallocene produces a high molecular weight component, and is generally a tightly bridged metallocene containing a substituent that includes a terminal olefin. The second metallocene, used to produce the low molecular weight component, is generally not bridged and is more responsive to hydrogen than the first metallocene. The combination of metallocenes is used with an activator-support and an organoaluminum compound to form polyolefins having an excellent balance of stiffness and slow crack growth resistance.

Catalyst compositions including various combinations of these metallocenes including, but not limited to, at least one first metallocene compound, at least one second metallocene compound, and any combination of more than one first metallocene compound, more than one second metallocene compound are also contemplated by this invention. Further, use of more than one activator-support and more than one organoaluminum compound is also contemplated.

1. The Metallocene Compounds ’ (a) The First Metallocene Compound

According to one aspect of the present invention, the first metallocene compound is an ansa-metallocene compound having the formula:

CA 02824482 2013-08-22 (X1)(X2R‘2)(X3)(X4)M1 (I);

wherein (X1) is cyclopentadienyl, indenyl, or fluorenyl; (X2) is fluorenyl; (X1) and (X2) are connected by a disubstituted bridging group comprising one atom bonded to both (X1) and (X2), wherein the atom is carbon or silicon; a first substituent of the disubstituted bridging group comprises an aliphatic or aromatic group having from 1 to about 10 carbon atoms; a second substituent of the disubstituted bridging group is a saturated or unsaturated aliphatic group having from 3 to about 10 carbon atoms; R1 is H or an alkyl group having from 1 to about 4 carbon atoms; (X3) and (X4) independently are a halide; and M1 is Zr or Hf.

According to one aspect of'the present invention, the first substituent of the disubstituted bridging group may be phenyl or methyl. The second substituent of the disubstituted bridging group may be butenyl, pentenyl, or hexenyl. In this and other aspects, (X3) and (X4) may be the same or different

According to yet another aspect of the present invention, the first metallocene compound is an ansa-metallocene compound having the formula:

(X’)CK2R,^)(X3)(X4)M,;

wherein (X') is cyclopentadienyl, indenyl, or fluorenyl; (X2) is fluorenyl; (X1) and (X2) are connected by a disubstituted bridging group comprising one atom bonded to both (X1) and (X2), wherein the atom is carbon or silicon; a first substituent of the disubstitnted bridging group comprises an aliphatic or aromatic group having from 1 to about 6 carbon atoms; a second substituent of the disubstituted bridging group is a saturated or unsaturated aliphatic group having from 3 to about 6 carbon atoms; R1 is an alkyl group having from 1 to about 4 carbon, atoms; (X3) and (X4) independently are a halide; and M1 is Zr or Hf.

According to one aspect of the present invention, the first substituent of tire disubstituted bridging group may be phenyl or methyl. According to another aspect of the present invention, the second substituent of the disubstituted bridging group may be butenyl, pentenyl, or hexenyl.

Some examples of metallocene compounds that may be suitable for use as the first metallocene compound in accordance with the present invention include, but are not limited to;

CA 02824482 2013-08-22

Additional examples of metallocene compounds that may be suitable for use as the first metallocene compound in accordance with the present invention include,

CA 02824482 2013-08-22

or any combination thereof.

(b) The Second Metallocene Compound

The second metallocene compound used in accordance with the present invention is characterized by poorer comonomer incorporation than Ind2ZrC12. Further, the second metallocene exhibits higher polymerization activity than

CA 02824482 2013-08-22

Ind2ZrCl2, The catalysts are amply, and positively, responsive to hydrogen, affording a low molecular weight polymer while maintaining high activity.

In accordance with the present invention, the second metallocene compound is an unbridged metallocene compound having the formula:

wherein R2 is H or -CH3; and R3 is CH2=CHCH2-, CH2^CH(CH2)2-, Ph(CH2)3-, CH3(CH2)3, or H; Xs and X6 independently are a halide; and M2 is Zr or Hf. In this and other aspects, (X5) and (X6) may be the same or different. Examples of 10 metallocene compounds that may be suitable for use as the second metallocene . compound in accordance with the present invention include, but are not limited to: ·

CA 02824482 2013-08-22

any combination thereof.

In this and other aspects of the present invention, the ratio of the first metallocene compound to the second metallocene compound may be from about 1:10 to about 10:1. In yet other aspects of the present invention, the ratio of the first metallocene compound to the second metallocene compound may be from about 1:5 to about 5:1. In still other aspects of the present invention, the ratio of the first

CA 02824482 2013-08-22 metallocene compound to the second metallocene compound may be from about 1:2 to about 2:1.

The present invention also provides a method for preparing 5 monocyclopentadienyl complexes (“half-metallocene compounds”) that results in greater yield of the desired compound. The present invention further provides a method of isolating the desired compound as a solid. While various exemplary compounds are provided herein, it should be understood that the method of the present invention may be used to prepare numerous other half-metallocene compounds. In one aspect, the half-metallocene compounds formed according to the present invention may be used to form metallocene compounds that are suitable for use in a dual catalyst system.

The presently known method of preparing a monocyclopentadienyl complex comprises adding solid ZrCU into a stirring solution of ZrCpzCh or a substituted Cp 15 analogue in toluene at ambient temperature and stirring for about 1 hour. The resulting mixture is filtered to yield the desired product as a dark oil. Using this method to make such compounds,- th$ resulting mixture consists primarily of unreacted starting material zirconocene dichloride.

According to the present invention, the reaction mixture is refluxed in 20 toluene for about 20 hours. By doing so, the reaction is nearly quantitative as compared with the presently known room temperature synthesis.

Toluene/Reflux (l,3R2R4Cp)2MCl2+ MOU----------► 2(1,3 R2R4Cp)MCl3 wherein M is Zr or Hf; R2 is H, an alkyl group, or an alkenyl group, and R4 is H, an alkyl group, or an alkenyl group. In one aspect, R2 is an alkyl group and R4 is H or an alkyl group. Thus, examples of half-metallocene compounds that may be formed according to the present invention include, but are not limited to Zî^-CsHa30 (nBu)]Cl3 and Zr^-C5H3-(nBu, Me)l,3]Cl3.

CA 02824482 2013-08-22

According to another aspect of the present invention, the desired halfmetallocene compound optionally is isolated as a solid. The solid is fonned by contacting the reaction mixture with CH2CI2 and pentane, hexane, heptane, or any combination thereof. In one aspect, the solid is formed by contacting the reaction mixture with a mixture of CH2CI2 and pentane to yield the trichlorides as a solid. The ratio of CH2CI2 to pentane maybe 1:2,1:3,1:4,1:5, or 1:6, or any other suitable ratio. Alternatively, a mixture of CH2CI2 with hexane may be used. Alternatively still, a mixture of CH2CI2 with heptane may be used. The amount of CH2C12/pentane mixture used may vary for each reaction mixture, for example, for 38g of (nBuCp)2ZrC12 about 150 mL CH2CI2 and 300 mL of pentane may be used.

The reaction mixture may be contacted several times with the CHaCWpentane mixture if necessary or desired. In one aspect, the reaction mixture may be contacted with the CHaClj/pentane mixture one time. In another aspect, the reaction mixture may be contacted with the CHaC^/pentane mixture two times. In another aspect, the reaction mixture may be contacted with the CHzCWpentane mixture three times. In yet another aspect, the reaction mixture may be contacted with the CH^Ch/pentane mixture four or more times.

This method provides the half- metallocene compound in at least about 50% yield. In one aspect, the method of the present invention provides the halfmetallocene compound in at least about 60% yield. In another aspect, the method of the present invention provides the half- metallocene compound in at least about 70% yield. In yet another aspect, the method of the present invention provides the halfmetallocene compound in at least about 80% yield. In still another aspect, the method of the present invention provides the half- metallocene compound in at least about 90% yield. In a still further aspect, the method of the present invention provides the half-metallocene compound in at least about 95% yield.

2. The Activator-Support

The present invention encompasses various catalyst compositions including an activator-support comprising a chemically-treated solid oxide. Alternatively, the activator-support may comprise a pillared clay.

CA 02824482 2013-08-22

The chemically-treated solid oxide exhibits enhanced acidity as compared to the corresponding untreated solid oxide compound. The chemically-treated solid oxide also functions as a catalyst activator as compared to the corresponding untreated solid oxide. While the chemically-treated solid oxide activates the metallocene in the absence of cocatalysts, it is not necessary to eliminate cocatalysts from the catalyst composition. The activation function of the activator-support is evident in the enhanced activity of catalyst composition as a whole, as compared to a catalyst composition containing the corresponding untreated solid oxide. However, it is believed that the chemically-treated solid oxide can function as an activator, even in the absence of an organoaluminum compound, aluminoxanes, organoboron compounds, or ionizing ionic compounds.

The chemically-treated solid oxide may comprise at least one solid oxide treated with at least one electron-withdrawing anion. While not intending to be bound by the following statement, it is believed that treatment of the solid oxide with an electron-withdrawing component augments or enhances the acidity of the oxide. Thus, the activator-support exhibits Lewis or Bransted acidity that is typically greater than the Lewis or Bransted acid strength than the untreated solid oxide, or the activator-support has a greater number of acid sites than the untreated solid oxide, or both. One method to quantify the acidity of the chemically-treated and untreated solid oxide materials is by comparing the polymerization activities of the treated and untreated oxides under acid catalyzed reactions. ·

The chemically-treated solid oxide of this invention is formed generally from an inorganic solid oxide having a relatively high porosity that exhibits Lewis acidic or Brensted acidic behavior. The solid oxide is chemically-treated with an electronwithdrawing component, typically an electron-withdrawing anion, to form an activator-support.

According to one aspect of the present invention, the solid oxide used to prepare the chemically-treated solid oxide may have a pore volume greater than about 0.1 cc/g. According to another aspect of the present invention, the solid oxide may have a pore volume greater than about 0.5 cc/g. According to yet another aspect

CA 02824482 2013-08-22 of the present invention, the solid oxide may have a pore volume greater than about 1.0 cc/g.

According to another aspect of the present invention, the solid oxide may 2 have a surface area of from about 100 to about 1000 m /g. According to yet another aspect of the present invention, the solid oxide may have a surface area of from about 200 to about 800 m /g. According to still another aspect of the present. invention, the solid oxide may have a surface area of from about 250 to about 600 2, m /g.

The chemically-treated solid oxide may comprise a solid inorganic oxide comprising oxygen and at least one element selected from Group 2,3,4,5, 6, 7, 8,9, 10, 11,12,13,14, or 15 of the periodic table, or comprising oxygen and at least one element selected from the lanthanide or actinide elements. (See: Hawley's Condensed Chemical Dictionary, 11th Ed., John Wiley & Sons; 1995; Cotton, F.A.; Wilkinson, G.; Murillo; C. A.; and Bochmann; M. Advanced Inorganic Chemistry, 6,h Ed., Wiley-Interscience, 1999). For example, the inorganic oxide may comprise oxygen and at least one element selected from Al, B, Be, Bi, Cd, Co, Cr, Cu, Fe, Ga, La, Mn, Mo, Ni, Sb, Si, Sn, Sr, Th, Ti, V, W, P, Y, Zn or Zr.

Suitable examples of solid oxide materials or compounds that can be used to form the chemically-treated solid oxide include, but are not limited to, A12O3, B2O3, BeO, Bi2O3, CdO, Co3O4, Cr2O3, CuO, Fe2O3, Ga2O3, La2O3, Mn2O3s MoO3, NiO, P2O5, Sb2Os, SiO2, SnO2, SrO, ThO2, TiO2, V2OS, WO3, Y2O3, ZnO, ZrO2> and the like, including mixed oxides thereof, and combinations thereof. For example, the solid oxide may be silica, alumina, silica-alumina, aluminum phosphate, heteropolytungstates, titania, zirconia, magnesia, boria, zinc oxide, mixed oxides thereof, or any combination thereof.

The solid oxide of this invention encompasses oxide materials such as alumina, “mixed oxide” compounds thereof such as silica-alumina, and combinations and mixtures thereof. The mixed oxide compounds such as silicaalumina can be single or multiple chemical phases with more than one metal combined with oxygen to form a solid oxide compound. Examples of mixed oxides

CA 02824482 2013-08-22 that can be used in the activator-support of the present invention include, but are not limited to, silica-alumina, silica-titania, silica-zirconia, zeolites, various clay minerals, alumina-titania, alumina-zirconia, zinc-aluminate and the like.

The electron-withdrawing component used to treat the solid oxide may be any component that increases the Lewis or Brmisted acidity of the solid oxide upon treatment (as compared to the solid oxide that is not treated with at least one electron-withdrawing anion). According to one aspect of the present invention, the electron-withdrawing component is an electron-withdrawing anion derived from a salt, an acid, or other compound, such as a volatile organic compound, that may serve as a source or precursor for that anion. Examples of electron-withdrawing anions include, but are not limited to, sulfate, bisulfate, fluoride, chloride, bromide, iodide, fluorosulfate, fluoroborate, phosphate, fluorophosphate, trifluoroacetate, triflate, fluorozirconate, fluorotitanate, trifluoroacetate, triflate, and the like, including mixtures and combinations thereof. In addition, other ionic or non-ionic compounds that serve as sources for these electron-withdrawing anions may also be employed in the present invention.

. Thus, for example,, the chemically-treated solid oxide used with the present invention may be fluorided alumina, chlorided alumina, bromided alumina, sulfated alumina, fluorided silica-alumina, chlorided silica-alumina, bromided silica-alumina, sulfated silica-alumina, fluorided silica-zirconia, chlorided silica-zirconia, bromided silica-zirconia, sulfated silica-zirconia, or any combination thereof.

When the electron-withdrawing component comprises a salt of an electronwithdrawing anion, the counterion or cation of that salt may be selected from any cation that allows the salt to revert or decompose back to the acid during calcining. Factors that dictate the suitability of the particular salt to serve as a source for the electron-withdrawing anion include, but are not limited to, the solubility of the salt in the desired solvent, the lack of adverse reactivity of the cation, ion-pairing effects between the cation and anion, hygroscopic properties imparted to the salt by the cation, and the like, and thermal stability of the anion. Examples of suitable cations in the salt of the electron-withdrawing anion include, but are not limited to,

CA 02824482 2013-08-22 ammonium, trialkyl ammonium, tetraalkyl ammonium, tetraalkyl phosphonium, H4, [H(OEt2)2]+, and the like.

Further, combinations of one or more different electron-withdrawing anions, in varying proportions, can be used to tailor the specific acidity of the activatorsupport to tlie desired level. Combinations of electron-withdrawing components may be contacted with the oxide material simultaneously or individually, and in any order that affords the desired chemically-treated solid oxide acidity. For example, one aspect of this invention is employing two or more electron-withdrawing anion source compounds in two or more separate contacting steps.

Thus, one example of such a process by which an chemically-treated solid oxide is prepared is as follows: a selected solid oxide compound, or combination of oxide compounds, is contacted with a first electron-withdrawing anion source compound to form a first mixture; Ihis first mixture is calcined and then contacted with a second electron-withdrawing anion source compound to form a second mixture; the second mixture is then calcined to form a treated solid oxide compound. In such a process, the first and second electron-withdrawing anion source compounds may be different compounds or the same compound. ·

According to another aspect of the present invention, the chemically-treated solid oxide may comprise a solid inorganic oxide material, a mixed oxide material, or a combination of inorganic oxide materials, that is chemically-treated with an electron-withdrawing component, and optionally treated with a metal source, including metal salts, metal ions, or other metal-containing compounds. The metal or metal ion may be, for example, zinc, nickel, vanadium, titanium, silver, copper, gallium, tin, tungsten, molybdenum, or any combination thereof. Examples of chemically-treated solid oxides that include a metal or metal ion include, but are not limited to, zinc-impregnated chlorided alumina, titanium-impregnated fluorided alumina, zinc-impregnated fluorided alumina, zinc-impregnated chlorided silicaalumina, zinc-impregnated fluorided silica-alumina, zinc-impregnated sulfated alumina, chlorided zinc aluminate, fluorided zinc aluminate, sulfated zinc aluminate, or any combination thereof.

CA 02824482 2015-01-26

Any method of impregnating the solid oxide material with a metal may be used. The method by which the oxide is contacted with a metal source, typically a salt or metal-containing compound, may include, but is not limited to, gelling, cogelling, impregnation of one compound onto another, and the like. If desired, the 5 metal-containing compound may be added to or impregnated into the solid oxide in solution form, and subsequently converted into the supported metal upon calcining. Accordingly, the solid inorganic oxide can further comprise a metal selected from zinc, titanium, nickel, vanadium, silver, copper, gallium, tin, tungsten, molybdenum, or a combination thereof. For example, zinc may be used to impregnate the solid 10 oxide because it provides good catalyst activity and low cost.

The solid oxide may be treated with metal salts or metal-containing compounds before, after, or at the same time that the solid oxide is treated with the electron-withdrawing anion. Following any contacting method, the contacted mixture of oxide compound, electron-withdrawing anion, and the metal ion is 15 typically calcined. Alternatively, a solid oxide material, an electron-withdrawing anion source, and the metal salt or metal-containing compound are contacted and calcined simultaneously. ...

Various processes may be used to form the chemically-treated solid oxide.

The chemically-treated solid oxide may comprise the contact product of at least one 20 solid oxide compound and at least one electron-withdrawing anion source. It is not required that the solid oxide compound be calcined prior to contacting the electronwithdrawing anion source. The contact product may be calcined either during or after the solid oxide compound is contacted with the electron-withdrawing anion source. The solid oxide compound may be calcined or uncalcined. Various 25 processes to prepare solid oxide activator-supports that can be employed in this invention have been reported. For example, such methods are described in U.S. Patent Nos. 6,107,230, 6,165,929, 6,294,494, 6,300,271, 6,316,553, 6,355,594,. 6,376,415, 6,391,816, 6,395,666, 6,524,987, and 6,548,441. . each of which may be referred to for further details.

According to one aspect of the present invention, the solid oxide material may be chemically-treated by contacting it with at least one electron-withdrawing

CA 02824482 2013-08-22 component, typically an electron-withdrawing anion source. Further, the solid oxide material optionally may be chemically treated with a metal ion, and then calcined to form a metal-containing or metal-impregnated chemically-treated solid oxide. According to another aspect of the present invention, the solid oxide material and electron-withdrawing anion source are contacted and calcined simultaneously.

The method by which the oxide is contacted with the electron-withdrawing component, typically a salt or an acid of an electron-withdrawing anion, may include, but is not limited to, gelling, co-gelling, impregnation of one compound onto another, and the like. Thus, following any contacting method, the contacted mixture of the solid oxide, electron-withdrawing anion, and optional metal ion, is calcined.

The solid oxide activator-support (chemically-treated solid oxide) may thus be produced by a process comprising:

1) contacting a solid oxide compound with at least one electronwithdrawing anion source compound to form a first mixture; and

2) calcining the first mixture to form the solid oxide activator-support.

According to another aspect of the present invention, the solid oxide activator-support (chemically-treated solid oxide) may be produced by a process comprising:

1) contacting at least one solid oxide compound with a first electronwithdrawing anion source compound to form a first mixture;

2) calcining the first mixture to produce a calcined first mixture;

3) contacting the calcined first mixture with a second electron- withdrawing anion source compound to form a second mixture; and

4) calcining the second mixture to form the solid oxide activatorsupport.

According to yet another aspect of the present invention, the chemicallytreated solid oxide is produced or formed by contacting the solid oxide with the electron-withdrawing anion source compound, where the solid oxide compound is calcined before, during, or after contacting the electron-withdrawing anion source, and where there is a substantial absence of aluminoxanes and organoborates.

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Calcining of the treated, solid oxide generally is conducted in an ambient atmosphere, typically in a dry ambient atmosphere, at a temperature from about 200°C to about 900°C, for about 1 minute to about 100 hours. Calcining may be conducted at a temperature of from about 300°C to about 800°C, for example, at a temperature of from about 400°C to about 700°C. Calcining may bo conducted for about 1 hour to about 50 hours, for example, for about 3 hours to about 20 hours. Thus, for example, calcining may be carried out for about 1 to about 10 hours at a temperature of from about 350°C to about 550°C. Any type of suitable ambient can be used during calcining. Generally, calcining is conducted in an oxidizing atmosphere, such as air. Alternatively, an inert atmosphere, such as nitrogen or argon, or a reducing atmosphere, such as hydrogen or carbon monoxide, may be used.

According to one aspect of the present invention, the solid oxide material may be treated with a source of halide ion, sulfate ion, or a combination of anions, optionally treated with a metal ion, and then calcined to provide the chemicallytreated solid oxide in the form of a particulate solid. For example, the solid oxide material may be treated-with a source of sulfate (termed a “sulfating agent”), à source of chloride ion (termed a “chloriding agent”), a source of fluoride ion (termed a “fluoriding agent”), or a combination thereof, and calcined to provide the solid oxide activator. Useful acidic activator-supports include, but are not limited to, bromided alumina, chlorided alumina, fluorided alumina, sulfated alumina, bromided silica-alumina, chlorided silica-alumina, fluorided silica-alumina, sulfated silica-alumina, bromided silica-zirconia, chlorided silica-zirconia, fluorided silicazirconia, sulfated silica-zirconia; a pillared clay, such as a pillared montmorillonite, optionally treated with fluoride, chloride, or sulfate; phosphated alumina or other aluminophosphates optionally treated with sulfate, fluoride, or chloride; or any combination of the above. Further, any of the activator-supports optionally may be treated with a metal ion.

The chemically-treated solid oxide may comprise a fluorided solid oxide in the form of a particulate solid. The fluorided solid oxide may be formed by contacting a solid oxide with a fluoriding agent. The fluoride ion may be added to

CA 02824482 2013-08-22 the oxide by forming a slurry of the oxide in a suitable solvent such as alcohol or water including, but are not limited to, the one to three carbon alcohols because of their volatility and low surface tension. Examples of fluoriding agents that may be suitable include, but are not limited to, hydrofluoric acid (HF), ammonium fluoride (NH4F), ammonium bifluoride (NH4HF2), ammonium tetrafluoroborate (NH4BF4), ammonium silicofluoride (hexafluorosilicate) ((NEUjaSiFe), ammonium hexafluorophosphate (NFLjPFû), analogs thereof, and combinations thereof. For example, ammonium bifluoride NH4HF2 may be used as the fluoriding agent, due to its ease of use and ready availability.

If desired, the solid oxide may be treated with a fluoriding agent during the calcining step. Any fluoriding agent capable of thoroughly contacting the solid oxide during the calcining step can be used. For example, in addition to those fluoriding agents described previously, volatile organic fluoriding agents may be used. Examples of volatile organic fluoriding agents useful in this aspect of the invention include, but are not limited to, freons, perfluorohexane, perfluorobenzene, fluoromethane, trifluoroethanol, and combinations thereof. Gaseous hydrogen fluoride or fluorine itself also can be used with tire solid oxide is fluorided during calcining. One convenient method of contacting the solid oxide with the fluoriding agent is to vaporize a fluoriding agent into a gas stream used to fluidize the solid oxide during calcination.

Similarly, in another aspect of this invention, the chemically-treated solid oxide may comprise a chlorided solid oxide in the form of a particulate solid. The chlorided solid oxide may be formed by contacting a solid oxide with a chloriding agent. The chloride ion may be added to the oxide by forming a slurry of the oxide in a suitable solvent. The solid oxide may be treated with a chloriding agent during the calcining step. Any chloriding agent capable of serving as a source of chloride and thoroughly contacting the oxide during the calcining step may be used. For example, volatile organic chloriding agents may be used. Examples of volatile organic chloriding agents that may be suitable include, but are not limited to, certain freons, perchlorobenzene, chloromethane, dichloromethane, chloroform, carbon tetrachloride, trichloroethanol, or any combination thereof. Gaseous hydrogen

CA 02824482 2013-08-22 chloride or chlorine itself may also be used with the solid oxide during calcining.

One convenient method of contacting the oxide with the chloriding agent is to vaporize a chloriding agent into a gas stream used to fluidize the solid oxide during calcination.

The amount of fluoride or chloride ion present before calcining the solid oxide may be from about 2 to about 50% by weight, where weight percent is based on the weight of the solid oxide, for example, silica-alumina, before calcining. According to another aspect of this invention, the amount of fluoride or chloride ion present before calcining the solid oxide may be from about 3 to about 25% by weight, and according to another aspect of this invention, may be from about 4 to about 20% by weight. Once impregnated with halide, the halided oxide may be dried by any method known in the art including, but not limited to, suction filtration followed by evaporation, drying under vacuum, spray drying, and the like, although it is also possible to initiate the calcining step immediately without drying the impregnated solid oxide.

The silica-alumina used to prepare the treated silica-alumina typically has a pore volume greater than about 0.5 cc/g. According to one aspect of the present invention, the pore volume may be greater than about 0.8 cc/g, and according to another aspect of the present invention, the pore volume may be greater than about 1.0 cc/g. Further, the silica-alumina may have a surface area greater than about 100 m2/g. According to one aspect of this invention, the surface areamay be greater than about 250 m2/g, and according to another aspect of this invention, the surface area I may be greater than about 350 m2/g.

The silica-alumina used with the present invention typically has an alumina content from about 5 to about 95%. According to one aspect of this invention, the alumina content of the silica-alumina may be from about 5 to about 50%, and according to another aspect of this invention, the alumina content of the silicaalumina may be from about 8% to about 30% alumina by weight. According to yet another aspect of this invention, the solid oxide component may comprise alumina without silica, and according to another aspect of this invention, the solid oxide component may comprise silica without alumina.

CA 02824482 2013-08-22

The sulfated solid oxide comprises sulfate and a solid oxide component, such as alumina or silica-alumina, in the form of a particulate solid. Optionally, the sulfated oxide may be treated further with a metal ion such that the calcined sulfated oxide comprises a metal. According to one aspect of the present invention, the sulfated solid oxide comprises sulfate and alumina. In some instances, the sulfated alumina is formed by a process wherein the alumina is treated with a sulfate source, for example, but not limited to, sulfuric acid or a sulfate salt such as ammonium sulfate. This process may be performed by forming a slurry of the alumina in a suitable solvent, such as alcohol or water, in which the desired concentration of the sulfating agent has been added. Suitable organic solvents include, but are not limited to, the one to three carbon alcohols because of their volatility and low surface tension.

According to one aspect of this invention, the amount of sulfate ion present before calcining may be from about 0.5 parts by weight to about 100 parts by weight sulfate ion to about 100 parts by weight solid oxide. According to another aspect of this invention, the amount of sulfate ion present before calcining may be from about 1 part by weight to about 50 parts by weight sulfate ion to about 100 parts by weight solid oxide, and according to still another aspect of this invention, from about 5 parts by weight to about 30 parts by weight sulfate ion to about 100 parts by weight solid oxide. These weight ratios are based on the weight of the solid oxide before calcining. Once impregnated with sulfate, the sulfated oxide may be dried by any method known in the art including, but not limited to, suction filtration followed by evaporation, drying under vacuum, spray drying, and the like, although it is also possible to initiate tire calcining step immediately.

According to another aspect of the present invention, activator-support comprises a pillared clay. The term “pillared clay” is used to refer to clay materials that have been ion exchanged with large, typically polynuclear, highly charged metal complex cations. Examples of such ions include, but are not limited to, Keggin ions which can have charges such as 7+, various polyoxometallates, and other large ions. Thus, the term pillaring refers to a simple exchange reaction in which the exchangeable cations of a clay material are replaced with large, highly charged ions,

CA 02824482 2015-01-26 such as Keggin ions. These polymeric cations are then immobilized within the interlayers of the clay and when calcined are converted to metal oxide “pillars”, effectively supporting the clay layers as column-like structures. Thus, once the clay is dried and calcined to produce the supporting pillars between clay layers, the 5 expanded lattice structure is maintained and the porosity is enhanced. The resulting pores can vary in shape and size as a function of the pillaring material and the parent clay material used. Examples of pillaring and pillared clays are found in: TJ. Pinnavaia, Science 220 (4595), 365-371 (1983); J.M. Thomas, Intercalation Chemistry, (S. Whittington and A. Jacobson, eds.) Ch. 3, pp. 55-99, Academic Press, 10 Inc., (1972); U.S. Patent No. 4,452,910; U.S. Patent No. 5,376,611; and U.S. Patent

No. 4,060,480; each of which may be referred to for further details.

The pillaring process utilizes clay minerals having exchangeable cations and layers capable of expanding. Any pillared clay that can enhance the polymerization of olefins in the catalyst composition of the present invention may be used.

Therefore, suitable clay minerals for pillaring include, but are not limited to: allophanes; smectites, both dioctahedral (Al) and tri-octahedral (Mg) and derivatives thereof such as montmorillonites (bentonites), nontronites, hectorites, or laponites; halloysites; vermiculites; micas; fluoromicas; chlorites; mixed-layer clays; the fiberous clays including but not limited to sepiolites, attapulgites, and palygorskites;

a serpentine clay; illite; laponite; saponite; and any combination thereof. In one aspect, the pillared clay activator-support comprises bentonite or montmorillonite. The principal component of bentonite is montmorillonite.

The pillared clay may be pretreated if desired. For example, a pillared bentonite may be preheated by drying at about 300°C under an inert atmosphere, 25 typically dry nitrogen, for about 3 hours, before being added to the polymerization reactor. Although an exemplary pretreatment is described herein, it should be understood that the preheating can be carried out at many other temperatures and times, including any combination of temperature and time steps, all of which are encompassed by this invention.

The activator-support used to prepare the catalyst compositions of the present invention may be combined with other inorganic support materials, including, but

CA 02824482 2013-08-22 are not limited to, zeolites, inorganic oxides, phosphated inorganic oxides, and the like. In one aspect, typical support materials that may be used include, but are not limited to, silica, silica-alumina, alumina, titania, zirconia, magnesia, boria, fiuorided alumina, silated alumina, thoria, aluminophosphate, aluminum phosphate, phosphated silica, phosphated alumina, silica-titania, coprecipitated silica/titania, fluorided/silated alumina, and any combination or mixture thereof.

According to yet another aspect of the present invention, one or more of the metallocene compounds may be precontacted with an olefin monomer and an organoaluminum compound for a first period of time prior to contacting this mixture with flte activator-support. Once the precontacted mixture of the metallocene compound(s), olefin monomer, and organoaluminum compound is contacted with the activator-support, the composition further comprising the activator-support is termed the “postcontacted” mixture. The postcontacted mixture may be allowed to remain in further contact for a second period of time prior to being charged into the reactor in which the polymerization process will be carried out.

3. The Organoaluminum Compound

Organoaluminum compounds that may be used with the present invention include, but are not limited to, compounds having the formula:

(R2)3A1;

where (R2) is an aliphatic group having from 2 to about 6 carbon atoms. For example, (R2) may be an ethyl group, a propyl group, a butyl group, a hexyl group, or an isobutyl group.

Other organoaluminum compounds that may be used in accordance with the present invention include, but are not limited to, compounds having the formula:

AlfX^X'V, where (X9) is a hydrocarbyl having from 1 to about 20 carbon atoms, (X10) is an alkoxide or an aiyloxide, any one of which having from 1 to about 20 carbon atoms, a halide, or a hydride, and n is a number from 1 to 3, inclusive. According to one aspect of the present invention, (X9) is an alkyl having from 1 to about 10 carbon atoms. Examples of (X9) moieties include, but are not limited to, ethyl, propyl, nbutyl, sec-butyl, isobutyl, hexyl, and the like. According to another aspect of the

CA 02824482 2013-08-22 present invention, (X10) may be independently selected from fluoro or chloro. According to yet another aspect of the present invention, (X10) may be chloro. In the formula Al(X9)n(XI0)3.n, n is a number from 1 to 3 inclusive, and typically, n is 3. The value of n is not restricted to be an integer, therefore, this formula includes sesquihalide compounds or other organoaluminum cluster compounds.

Examples of organoaluminum compounds that may be suitable for use with the present invention include, but are not limited to, trialkylaluminum compounds, dialkylaluminium halide compounds, dialkylaluminum alkoxide compounds, dialkylaluminum hydride compounds, and combinations thereof. Specific examples of organoaluminum compounds that may be suitable include, but are not limited to: trimethylaluminum (TMA), triethylaluminum (TEA), tripropylaluminum, diethylaluminum ethoxide, tributylaluminum, disobutylaluminum hydride, triisôbutylaluminum (ΊΊΒ A), and diethylaluminum, chloride.

The present invention contemplates precontacting the first metallocene compound, the second metallocene compound, or both, with at least one organoaluminum compound and an olefin monomer to form a precontacted mixture,. prior to contacting this precontacted mixture with the activator-support to form the active catalyst. When the catalyst composition is prepared in this manner, typically, though not necessarily, a portion of the organoaluminum compound is added to the precontacted mixture and another portion of the organoaluminum compound is added to the postcontacted mixture prepared when the precontacted mixture is contacted with the solid oxide activator. However, tire entire organoaluminum compound may be used to prepare the catalyst in either the precontacting or postcontacting step. Alternatively, all the catalyst components may be contacted in a single step.

Further, more than one organoaluminum compound may be used in either the precontacting or the postcontacting step. When an organoaluminum compound is added in multiple steps, the amounts of organoaluminum compound disclosed herein include the total amount of organoaluminum compound used in both the precontacted and postcontacted mixtures, and any additional organoaluminum compound added to the polymerization reactor. Therefore, total amounts of

CA 02824482 2013-08-22 organoaluminum compounds are disclosed regardless of whether a single organoaluminum compound or more than one organoaluminum compound is used.

4. The Optional Aluminoxane Cocataivst

The present invention further provides a catalyst composition comprising an optional aluminoxane cocatalyst. As used herein, the term “aluminoxane” refers to aluminoxane compounds, compositions, mixtures, or discrete species, regardless of how such aluminoxanes are prepared, formed or otherwise provided. For example, a catalyst composition comprising an optional aluminoxane cocatalyst can be prepared in which aluminoxane is provided as the poly(hydrocarbyl aluminum oxide), or in which aluminoxane is provided as the combination of an aluminum allcyl compound and a source of active protons such as water. Aluminoxanes are also referred to as poly(hydrocarbyl aluminum oxides) or organoaluminoxanes.

The other catalyst components typically are contacted with the aluminoxane in a saturated hydrocarbon compound solvent, though any solvent that is substantially inert to the reactants, intermediates, and products of the activation step may be used. The catalyst composition formed in this manner may be collected by methods known to those of skill in the art including, but not limited to, filtration. Alternatively, the catalyst composition may be introduced into the polymerization reactor without being isolated.

The aluminoxane compound of this invention may be an oligomeric aluminum compound comprising linear structures, cyclic, or cage structures, or mixtures of all three. Cyclic aluminoxane compounds having the formula:

R wherein R is a linear or branched alkyl having from 1 to 10 carbon atoms, and n is an integer from 3 to about 10j are encompassed by this invention. The (AlR0)n moiety shown here also constitutes the repeating unit in a linear aluminoxane. Thus, linear aluminoxanes having the formula:

CA 02824482 2015-01-26

R r-4-ai-o-Vai \ I /nV . R ;

wherein R is a linear or branched alkyl having from 1 to 10 carbon atoms, and n is an integer from 1 to about 50, are also encompassed by this invention.

Further, aluminoxanes may also have cage structures of the formula

RSm+aR-bm-cAhniOam, wherein m is 3 or 4 and a is = iiai(3) - bq(2) + bo(4)> wherein nAi(3) is the number of three coordinate aluminum atoms, nop) is the number of two coordinate oxygen atoms, no(4) is the number of 4 coordinate oxygen atoms, R' is a terminal alkyl group, and Rb is a bridging alkyl group, and R is a linear or branched alkyl having from 1 to 10 carbon atoms.

Thus, aluminoxanes that may serve as optional cocatalysts in this invention are represented generally by formulas such as (R-Al-O)n, R(R-Al-O)nAlR2, and the like, wherein the R group is typically a linear or branched CrCe alkyl such as methyl, ethyl, propyl, butyl, pentyl, or hexyl, and n typically represents an integer ’ from 1 to about 50. Examples of aluminoxane compounds that may be used in 15 accordance with the present invention include, but are not limited to, methylaluminoxane, ethylaluminoxane, n-prppylaluminoxane, iso-propylaluminoxane, n-butylaluminoxane, t-butylaluminoxane, sec-butylaluininoxane, isobutylaluminoxane, 1-pentylaluminoxane, 2-pentylaluminoxane, 3-pentylaluminoxane, iso-pentylaluminoxane, neopentylaluminoxane, or any combination thereof. Methyl aluminoxane, ethyl aluminoxane, and isobutyl aluminoxane are prepared from frimethylaluminum, triethylaluminum, or triisobutylaluminum, respectively, and sometimes are referred to as poly(methyl aluminum oxide), poly(ethyl aluminum oxide), and poly(isobutyl aluminum oxide), respectively. It is also within the scope of the invention to use an aluminoxane in combination with a trialkylaluminum, such as that disclosed in U.S. Patent No. 4,794,096, which may be referred to for further details.

Tire present invention contemplates many values of n in the aluminoxane formulas (R-Al-O)n and R(R-Al-O)nAlR2, and n typically may be at least about 3.

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However, depending upon how the organoaluminoxane is prepared, stored, and used, the value of n may vary within a single sample of aluminoxane, and such combinations of organoaluminoxanes are contemplated hereby.

In preparing the catalyst composition of this invention comprising an 5 optional aluminoxane, the molar ratio of the aluminum in the aluminoxane to the metallocene in the composition may be &om about 1:10 to about 100,000:1, for example, from about 5:1 to about 15,000:1. The amount of optional aluminoxane added to a polymerization zone may be from about 0.01 mg/L to about 1000 mg/L, from about 0.1 mg/L to about 100 mg/L, or from about 1 mg/L to about 50 mg/L.

Organoaluminoxanes may be prepared by various procedures that are well known in the art. Examples of organoaluminoxane preparations are disclosed in U.S. Patent Nos. 3,242,099 and 4,808,56Leach of which may be referred to for further details. For example, water in an inert organic solvent may be reacted with an aluminum alkyl compound such as AIR3 to form the desired 15 organoaluminoxane compound. While not intending to be bound by this statement, it is believed that this synthetic method can afford a mixture of both linear and cyclic (R-Al-O)n aluminoxane species, both of which are encompassed by this invention. Alternatively, organoaluminoxanes may be prepared by reacting an aluminum allcyl compound, such as AIR3 with a hydrated salt, such as hydrated copper sulfate, in an 20 inert organic solvent.

5. The Optional Organoboron Cocatalyst

The present invention further provides a catalyst composition comprising an optional organoboron cocatalyst. The organoboron compound may comprise neutral boron compounds, borate salts, or any combination thereof. For example, the 25 organoboron compounds of this invention may comprise a fluoroorgano boron compound, a fluoroorgano borate compound, or a combination thereof.

Any fluoroorgano boron or fluoroorgano borate compound known in the art can be utilized with the present invention. Examples of fluoroorgano borate compounds that may be used as cocatalysts in the present invention include, but are 30 not limited to, fluorinated aryl borates such as Ν,Ν-dimethylanilinium tetrakis(pentafluorophenyl)borate, triphenylcarbenium tetrakis(pentafluorophenyl)borate,

CA 02824482 2015-01-26 lithium tetrakis(pentafluorophenyl)borate, Ν,Ν-dimethylanilinium tetrakis[3,5bis(trifluoromethyl)phenyl]borate, triphenylcarb enium tetrakis[3,5bis(trifluoromethyl)phenyl]borate, and the like, including mixtures thereof. Examples of fluoroorgano boron compounds that can be used as cocatalysts in the 5 present invention include, but are not limited to, tris(pentafluorophenyl)boron, tris[3,5-bis(trifluoromethyl)phenyl]boron, and the like, including mixtures thereof. Although not intending to be bound by the following theory, these examples of fluoroorgano borate and fluoroorgano boron compounds, and related compounds, are thought to form “weakly-coordinating” anions when combined with organometal compounds, as disclosed in U.S. Patent 5,919,983, which may be referred to for further details.

Generally, any amount of organoboron compound may be used. According to one aspect of this invention, the molar ratio of the organoboron compound to the metallocene compound in the composition may be from about 0.1:1 to about 10:1.

Typically, the amount of the fluoroorgano boron or fluoroorgano borate compound used as a cocatalyst for the metallocenes may be from about 0.5 mole to about 10 . . moles of boron compound per total moles of the metallocene compounds.

According to another aspect of this invention, the amount of fluoroorgano boron or fluoroorgano borate compound may be from about 0.8 mole to about 5 moles of 20 boron compound per total moles of the metallocene compound.

6. The Optional Ionizing Ionic Compound Cocatalyst

The present invention further provides a catalyst composition comprising an optional ionizing ionic compound cocatalyst. An ionizing ionic compound is an ionic compound that can function to enhance the activity of the catalyst composition.

While not intending to be bound by theory, it is believed that the ionizing ionic compound may be capable of reacting with a metallocene compound and converting the metallocene into one or more cationic metallocene compounds, or incipient cationic metallocene compounds. Again, while not intending to be bound by theory, it is believed that the ionizing ionic compound may function as an ionizing 30 compound by completely or partially extracting an anionic ligand, possibly a ηοη-η5alkadienyl ligand such as (X3) or (X4), from the metallocene. However, the ionizing

CA 02824482 2013-08-22 ionic compound is an activator regardless of whether it is ionizes the metallocene, abstracts an (X3) or (X4) ligand in a fashion as to form an ion pair, weakens the metal-(X3) or metal-(X4) bond in the metallocene, simply coordinates to an (X3) or (X4) ligand, or activates the metallocene by some other mechanism.

Further, it is not necessary that the ionizing ionic compound activate the metallocenes only. The activation function of the ionizing ionic compound is evident in the enhanced activity of catalyst composition as a whole, as compared to a catalyst composition containing catalyst composition that does not comprise any ionizing ionic compound. It is also not necessary that the ionizing ionic compound activate each of the metallocene compounds present, nor is it necessary that it activate the any of the metallocene compounds to the same extent.

Examples of ionizing ionic compounds include, but are not limited to, the following compounds: tri(n-butyl)ammonium tetrakis(p-tolyl)borate, tri(n-butyl)ammonium tetrakis(m-tolyl)borate, tri(n-butyl)annnonium tetrakis(2,4-dimethyl)borate, tri(n-butyl)ammonium tetrakis(3,5-dimethylphenyl)borate, tri(n-butyl)ammonium tetralds[3,5-bis(trifluoromethyl)phenyl]borate, tri(n-butyl)ammonium tetrakis(pentafluorophenyl)borate, Ν,Ν-dimethylanilinium tetrakis(p-tolyl)borate, Ν,Ν-dimethylanilinium tetrakis(m-tolyl)borate, Ν,Ν-dimethylanilinium tetralds(2,4dimethylphenyl)borate, Ν,Ν-dimethylanilinium tetrakis(3,5-dimethylphenyl)borate, Ν,Ν-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, Ν,Νdimethylanilinium tetrakis(pentafluorophenyl)borate, triphenylcarbenium tetrakis(ptolyl)borate, triphenylcarbenium tetrakis(m-tolyl)borate, triphenylcarbenium tetrakis(2,4-dimethylphenyl)borate, triphenylcarbenium tetrakis(3,5dimethylphenyl)borate, triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, triphenylcarbenium tetrakis(pentafluorophenyl)borate, tropylium tetrakis(p-tolyl)borate, tropylium tetrakis(m-tolyl)borate, tropylium tetrakis(2,4-dimethylphenyl)borate, tropylium tetrakis(3,5-dimethylphenyl)borate, tropylium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, tropylium tetrakis(pentafluorophenyl)borate, lithium tetralds(pentafluorophenyl)borate, lithium tetrakis(phenyl)borate, lithium tetrakis(p-tolyl)borate, lithium tetrakis(mtolyl)borate, lithium tetrakis(2,4-dimethylphenyl)borate, lithium tetrakis(3,539

CA 02824482 2013-08-22 dimethylphenyl)borate, lithium tetrafluoroborate, sodium tetrakis(pentafluorophenyl)borate, sodium tetrakis(phenyl) borate, sodium tetrakis(p-tolyl)borate, sodium tetralds(m-tolyl)borate, sodium tetrakis(2,4-dimethylphenyl)borate, sodium tetrakis(3,5-dimethylphenyl)borate, sodium tetrafluoroborate, potassium tetrakis(pentafluorophenyl)borate, potassium tetrakis(phenyl)borate, potassium tetrakis(ptolyl)borate, potassium tetrakis(m-tolyl)borate, potassium tetrakis(2,4-dimethylphenyl)borate, potassium tetrakis(3,5-dimethylphenyl)borate, potassium tetrafluoroborate, tri(n-butyl)ammonium tetrakis(p-tolyl)aluminate, tri(n-butyl)ammonium tetrakis(m-tolyl)aluminate, tri(n-butyl)ammonium tetrakis(2,4-dimethyl)aluminate, tri(n-butyl)ammonium tetrakis(3,5-dimethylphenyl)aluminate, tri(nbutyl)ammonium tetrakis(pentafluorophenyl)aluminate, Ν,Ν-dimethylanilinium tetrakis(p-tolyl)aluminate, Ν,Ν-dimethylanilinium tetrakis(m-tolyl)aluminate, N,Ndiméthylanilinium tetrakis(2,4-dimethylphenyl)aluminate, Ν,Ν-dimethylanilinium tetrakis(3,5-dimethylphenyl)aluminate, Ν,Ν-dimethylanilinium tetrakis (pentafluorophenyl)aluminate, triphenylcarbenium tetrakis(p-tolyl)aluminate, triphenylcafbenium tetrakis(m-tolyl)alnmmate, triphenylcarbenium tetrakis(2,4dimethylphenyl)aluminate, triphenylcarbenium tetralds(3,5dimethylphenyl)aluminate, triphenylcafbenium tetrakis(pentafluorophenyl)aluminate, tropylium tetrakis(p-tolyl)aluminate, tropylium tetrakis(m-tolyl)aluminate, tropylium tetrakis(2,4-dimethylphenyl)aluminate, tropylium tetrakis(3,5-dimethylphenyl)aluminate, tropylium tetrakis(pentafluorophenyl)aluminate, lithium tetrakis(pentafluorophenyl)aluminate, lithium tetrakis(phenyl)aluminate, lithium tetrakis(p-tolyl)aluminate, lithium tetrakisfmtolyl)aluminate, lithium tefrakis(2,4-dimethylphenyl)aluminate, lithium tetrakis(3,5dimethylphenyl) aluminate, lithium tetrafluoroaluminate, sodium tetralds(pentafluorophenyl)aluminate, sodium tetrakis(phenyl)aluminate, sodium tetrakis(p-tolyl)aluminate, sodium tetrakis(m-tolyl)aluminate, sodium tetrakis(2,4dimethylphenyl)aluminate, sodium tetrakis(3,5-dimethylphenyl)aluminate, sodium tetrafluoroaluminate, potassium tetrakis(pentafluorophenyl)aluminate, potassium tetrakis(phenyl)aluminate, potassium tetrakis(p-tolyl)aluminate, potassium tetrakis(m-tolyl)aluminate, potassium tetfakis(2,4-dimethylphenyl)aluminate,

CA 02824482 2015-01-26 potassium tetrakis (3,5-dimethylphenyl)aIuminate, potassium tetrafluoroaluminate, and the like. However, the optional ionizing ionic compounds that are useful in this invention are not limited to these. Other examples of ionizing ionic compounds are disclosed in U.S. Patent Nos. 5,576,259 and 5,807,938, each of which may be referred to for further details.

B. Olefin Monomer

Unsaturated reactants that may be useful with catalyst compositions and polymerization processes of this invention include olefin compounds having from about 2 to about 30 carbon atoms per molecule and at least one olefinic double bond.

This invention encompasses homopolymerization processes using a single olefin such as ethylene or propylene, as well as copolymerization reactions with at least one different olefinic compound. The resulting copolymer may comprise a major amount of ethylene (>50 mole percent) and a minor amount of comonomer <50 mole percent), though this is not a requirement. The comonomers that may be 15 copolymerized with ethylene typically may have from three to about 20 carbon atoms in their molecular chain.

Acyclic, cyclic, polycyclic, terminal (a), internal, linear, branched, substituted, unsubstituted, functionalized, and non-functionalized olefins may be employed in this invention. For example, typical unsaturated compounds that may 20 be polymerized with the catalysts of this invention include, but are not limited to, propylene, 1-butene, 2-butene, 3-methyl-l-butene, isobutylene, 1-pentene, 2penteue, 3-methyl-l-pentene, 4-methyl-1-pentene, 1-hexene, 2-hexene, 3-hexene, 3ethyl-1-hexene, 1-heptene, 2-heptene, 3-heptene, the four normal octenes, the four normal nonenes, the five normal decenes, and mixtures of any two or more thereof.

Cyclic and bicyclic olefins, including but not limited to, cyclopentene, cyclohexene, norbomylene, norbomadiene, and the like, may also be polymerized as described above.

When a copolymer is desired, the monomer ethylene may be copolymerized with a comonomer. Examples of the comonomer include, but are not limited to, ' 30 propylene, 1-butene, 2-butene, 3-methyl-l-butene, isobutylene, 1-pentene, 2pentene, 3-methyl-l-pentene, 4-methyl-l-pentene, l-hexene, 2-hexene, 3-hexene, 341

CA 02824482 2013-08-22 ethyl-l-hexene, 1-heptene, 2-heptene, 3-heptene, the four normal octenes, the four normal nonenes, or the five normal decenes. According to one aspect of the present invention, the comonomer may be selected from 1-butene, 1-pentene, 1-hexene, 1octene, 1-decene, ot styrene.

The amount of comonomer introduced into a reactor zone to produce the copolymer generally may be from about 0.01 to about 50 weight percent comonomer based on the total weight of the monomer and comonomer. According to another aspect of the present invention, the amount of comonomer introduced into a reactor zone may be from about 0.01 to about 40 weight percent comonomer based on the total weight of the monomer and comonomer. According to still another aspect of the present invention, the amount of comonomer introduced into a reactor zone may be from about 0.1 to about 35 weight percent comonomer based on the total weight of the monomer and comonomer. Alternatively, the amount of comonomer introduced into a reactor zone may be any amount sufficient to provide the above concentrations by weight.

While not intending to be bound by this theory, where branched, substituted, or functionalized olefins are used as reactants, it is believed that steric hindrance- may impede and/or slow the polymerization process. Thus, branched and/or cyclic portion(s) of the olefin removed somewhat from the carbon-carbon double bond would not be expected to hinder the reaction in the way that the same olefin substituents situated more proximate to the carbon-carbon double bond might. According to one aspect of the present invention, at least one reactant for the catalyst compositions of this invention may be ethylene, so the polymerizations are either homopolymerizations or copolymerizations with a different acyclic, cyclic, terminal, internal, linear, branched, substituted, or unsubstituted olefin. In addition, the catalyst compositions of this invention may be used in the polymerization of diolefin compounds including, but not limited to, 1,3-butadiene, isoprene, 1,4-pentadiene, and 1,5-hexadiene.

C. Preparation of the Catalyst Composition

The present invention encompasses a catalyst composition comprising the contact product of a first metallocene compound, a second metallocene compound,

CA 02824482 2013-08-22 an activator-support, and an organoaluminum compound. This invention further encompasses methods of making the catalyst composition encompassing contacting a first metallocene compound, a second metallocene compound, an activatorsupport, and an organoaluminum compound, in any order. According to such methods, an active catalyst composition is obtained when the catalyst components are contacted in any sequence or order.

One or more of the metallocene compounds may be precontacted with an olefinic monomer if desired, not necessarily the olefin monomer to be polymerized, and an organoaluminum cocatalyst for a first period of time prior to contacting this precontacted mixture with the activator-support The first period of time for contact, the precontact time, between the metallocene compound or compounds, the olefinic monomer, and the organoaluminum compound typically may range from time about 0.1 hour to about 24 hours, for example, from about 0.1 to about 1 hour. Precontact times from about 10 minutes to about 30 minutes are also typical.

Once the precontacted mixture of the metallocene compound or compounds, olefin monomer, and organoaluminum cocatalyst is contacted with the activatorsupport, this composition (further comprising the activator-support) is termed the “postcontacted mixture”. The postcontacted mixture optionally may be allowed to remain in contact for a second period of time, the postcontact time, prior to initiating the polymerization process. Postcontact times between the precontacted mixture and the activator-support may range in time from about 0.1 hour to about 24 hours, for example, from about 0.1 hour to about 1 hour. The precontacting, the postcontacting step, or both may increase the productivity of the polymer as compared to the same catalyst composition that is prepared without precontacting or postcontacting. However, neither a precontacting step nor a postcontacting step is required.

The postcontacted mixture may be heated at a temperature and for a duration sufficient to allow adsorption, impregnation, or interaction of precontacted mixture and the activator-support, such that a portion of the components of the precontacted mixture is immobilized, adsorbed, or deposited thereon. Where heating is used, the postcontacted mixture may be heated from between about 0°F to about 150°F, for example, from about 40°F to about 95°F.

CA 02824482 2013-08-22

According to one aspect of this invention, the molar ratio of the total moles of the metallocene compounds to the organoaluminum compound may be from about 1:1 to about 1:10,000. According to another aspect of this invention, the molar ratio of the total moles of the metallocene compounds combined to the organoaluminum compound may be from about 1:1 to about 1:1,000. According to yet another aspect of this invention, the molar ratio of the total moles of the metallocene compounds combined to the organoaluminum compound may be from about 1:1 to about 1:100. These molar ratios reflect the ratio of the metallocene compounds to the total amount of organoaluminum compound in both the precontacted mixture and the postcontacted mixture combined.

When a precontacting step is used, the molar ratio of olefin monomer to total moles of metallocene compound combined in the precontacted mixture may be from about 1:10 to about 100,000:1, for example, from about 10:1 to about 1,000:1.

The weight ratio of the activator-support to the organoaluminum compound may be from about 1:5 to about 1,000:1. The weight ratio of the activator-support to the organoaluminum compound may be from about 1:3 to about 100:1, for example, from about 1:1 to about 50:1.

According to a further aspect of this invention, the weight ratio of the total moles of the metallocene compound combined to the activator-support may be from about 1:1 to about 1:1,000,000. According to yet another aspect of this invention, the weight ratio of the total moles of the metallocene compound combined to the activator-support may be from about 1:10 to about 1:10,000. According to still another aspect of this invention, the weight ratio of the total moles of the metallocene compound combined to the activator-support may be from about 1:20 to. about 1:1000.

Aluminoxane compounds are not required to form the catalyst composition of the present invention. Thus, the polymerization proceeds in the absence of ahiminoxanes. Accordingly, the present invention may use AlR3-type organoaluminum compounds and an activator-support in the absence of aluminoxanes. While not intending to be bound by theory, it is believed that the organoaluminum compound likely does not activate the metallocene catalyst in the

CA 02824482 2013-08-22 same manner as an organoaluminoxane. As a result, the present invention results in lower polymer production costs.

Additionally, no expensive borate compounds or MgCh are required to form the catalyst composition of this invention. Nonetheless, aluminoxanes, organoboron compounds, ionizing ionic compounds, organozinc compounds, MgCh, or any combination thereof optionally may be used in the catalyst composition of this invention. Further, cocatalysts such as aluminoxanes, organoboron compounds, ionizing ionic compounds, organozinc compounds, or any combination thereof optionally may be used as cocatalysts with the metallocene compound, either in the presence or in the absence of the activator-support, and either in the presence or in the absence of the organoaluminum compound.

According to one aspect of this invention, the catalyst activity of the catalyst of this invention may be greater than or equal to about 100 grams polyethylene per gram of chemically-treated solid oxide per hour (abbreviated gP/(gCTSO-hr)). According to another aspect of this invention, the catalyst of this invention may be characterized by an activity of greater than or equal to about 250 gP/(gCTSO-hr). According to still another aspect of this invention, the catalyst of this invention may be characterized by an activity of greater than or equal to about 500 gP/(gCTSO-hr). According to yet another aspect of this invention, the catalyst of this invention may be characterized by an activity of greater than or equal to about 1000 gP/(gCTSO-hr). According to a further aspect of this invention, the catalyst of this invention may be characterized by an activity of greater than or equal to about 2000 gP/(gCTSO-hr). This activity is measured under slurry polymerization conditions using isobutane as the diluent, at a polymerization temperature of about 90°C and an ethylene pressure of about 550 psig. The reactor should have substantially no indication of any wall scale, coating or other forms of fouling upon making these measurements.

Any combination of the metallocene compounds, the activator-support, the organoaluminum compound, and the olefin monomer, may be precontacted. When any precontacting occurs with an olefinic monomer, it is not necessary that the olefin

CA 02824482 2013-08-22 monomer used in the precontacting step be the same as the olefin to be polymerized. Further, when a precontacting step among any combination of the catalyst components is employed for a first period of time, this precontacted mixture may be used in a subsequent postcontacting step between any other combination of catalyst components for a second period of time. For example, all the catalyst components and 1-hexene may be used in a precontacting step for a first period of time, and this precontacted mixture may then be contacted with the activator-support to form a postcontacted mixture that is contacted for a second period of time prior to initiating the polymerization reaction. For example, the first period of time for contact, tire precontact time, between any combination of the metallocene compounds, the olefinic monomer, the activator-support, and the organoaluminum compound may be from about 0.1 hour to about 24 hours, for example, from about 0.1 to about 1 hour. Precontact times from about 10 minutes to about 30 minutes are also typical. The postcontacted mixture optionally may be allowed to remain in contact for a second period of time, the postcontact time, prior to initiating the polymerization process. According to one aspect of this invention, postcontact times between the precontacted mixture and any remaining catalyst components may be from about 0.1 hour to about 24 hours, for example, from about 0.1 hour to about 1 hour.

D. Use of the Catalyst Composition In Polymerization Processes

After catalyst activation, the catalyst composition is used to homopolymerize ethylene or copolymerize ethylene with a comonomer.

The polymerization temperature may be from about 60°C to about 280°Ç, for example, from about 70°C to about 110°C. The polymerization reaction typically begins in an inert atmosphere substantially free of oxygen and under substantially anhydrous conditions. For example, a dry, inert atmosphere such as dry nitrogen or dry argon may be used.

The polymerization reaction pressure may be any pressure that does not terminate the polymerization reaction, and is typically a pressure higher than the pretreatment pressures. According to one aspect of the present invention, the polymerization pressure may be from about atmospheric pressure to about 1000 psig. According to another aspect of the present invention, the polymerization pressure

CA 02824482 2015-01-26 may be from about 50 psig to about 800 psig. Further, hydrogen can be used in the polymerization process of this invention to control polymer molecular weight, Polymerizations using the catalysts of this invention may be carried out in any manner known in the ait. Such processes that may be suitable for use with the 5 present invention include, but are not limited to, slurry polymerizations, gas phase polymerizations, solution polymerizations, and multi-reactor combinations thereof. Thus, any polymerization zone known in the art to produce olefin-containing polymers can be utilized. For example, a stirred reactor may.be utilized for a batch process, or a loop reactor or a continuous stirred reactor may be used for a 10 continuous process.

A typical polymerization method is a slurry polymerization process (also known as the particle form process), which is well known in the art and is disclosed, for example, in U.S. Patent No. 3,248,179, which may be referred to for further details. Other polymerization methods of the present invention for slurry processes 15 are those employing a loop reactor of the type disclosed in U.S. Patent No.

3,248,179, which may be referred to for further details, and those utilized in a plurality of stirred reactors either in series, parallel, or combinations thereof, where the reaction conditions are different in the different reactors. Suitable diluents used in slurry polymerization are well known in the art and include hydrocarbons that are 20 liquids under reaction conditions. The term “diluent” as used in this disclosure does not necessarily mean an inert material, as this term is meant to include compounds and compositions that may contribute to polymerization process. Examples of hydrocarbons that may be used as diluents include, but are not limited to, cyclohexane, isobutane, n-butane, propane, n-pentane, isopentane, neopentane, and 25 n-hexane. Typically, isobutane may be used as the diluent in a slurry polymerization, as provided by U.S. Patent Nos. 4,424,341, 4,501,885, 4,613,484, 4,737,280, and 5,597,892, each of which may be referred to for further details.

Various polymerization reactors are contemplated by the present invention. 30 As used herein, “polymerization reactor” includes any polymerization reactor or polymerization reactor system capable of polymerizing olefin monomers to produce

CA 02824482 2013-08-22 homopolymers or copolymers of the present invention. Such reactors may be slurry reactors, gas-phase reactors, solution reactors, or any combination thereof. Gas phase reactors may comprise fluidized bed reactors or tubular reactors. Slurry reactors may comprise vertical loops or horizontal loops. Solution reactors may comprise stirred tank or autoclave reactors.

Polymerization reactors suitable for the present invention may comprise at least one raw material feed system, at least one feed system for catalyst or catalyst components, at least one reactor system, at least one polymer recovery system or any suitable combination thereof. Suitable reactors for die present invention further may comprise any one, or combination of, a catalyst storage system, an extrusion system, a cooling system, a diluent recycling system, or a control system. Such reactors may comprise continuous take-off and direct recycling of catalyst, diluent, and polymer. Generally, continuous processes may comprise the continuous introduction of a monomer, a catalyst, and a diluent into a polymerization reactor and the continuous removal from this reactor of a suspension comprising polymer particles and the diluent

Polymerization reactor systems of die present invention may comprise one type of reactor per system or multiple reactor systems comprising two or more types of reactors operated in parallel or in series. Multiple reactor systems may comprise reactors connected together to perform polymerization or reactors that are not connected. The polymer may be polymerized in one reactor under one set of conditions, and then transferred to a second reactor for polymerization under a different set of conditions.

According to one aspect of the invention, the polymerization reactor system may comprise at least one loop slurry reactor. Such reactors are known in the art and may comprise vertical or horizontal loops. Such loops may comprise a single loop or a series of loops. Multiple loop reactors may comprise both vertical and horizontal loops. The slurry polymerization is typically performed in an organic solvent that can disperse the catalyst and polymer. Examples of suitable solvents include butane, hexane, cyclohexane, octane, and isobutane. Monomer, solvent, catalyst and any comonomer may be continuously fed to a loop reactor where

CA 02824482 2013-08-22 polymerization occurs. Polymerization may occur at low temperatures and pressures. Reactor effluent may be flashed to remove the solid resin.

According to yet another aspect of this invention, the polymerization reactor may comprise at least one gas phase reactor. Such systems may employ a continuous recycle stream containing one or more monomers continuously cycled through the fluidized bed in the presence of the catalyst under polymerization conditions. The recycle stream may be withdrawn from the fluidized bed and recycled back into the reactor. Simultaneously, polymer product may be withdrawn from the reactor and new or fresh monomer may be added to replace the polymerized monomer. Such gas phase reactors may comprise a process for multi-step gas-phase polymerization of olefins, in which olefins are polymerized in the gaseous phase in at least two independent gas-phase polymerization zones while feeding a catalystcontaining polymer formed in a first polymerization zone to a second polymerization zone.

According to still another aspect of the invention, the polymerization reactor may comprise a tubular reactor. Tubular reactors may make polymers by free radical initiation, or by .employing the catalysts typically used for coordination polymerization. Tubular reactors may have several zones where fresh monomer, initiators, or catalysts are added. Monomer may be entrained in an inert gaseous stream and introduced at one zone of the reactor. Initiators, catalysts, and/or catalyst components may be entrained in a gaseous stream and introduced at another zone of the reactor. The gas streams may be intermixed for polymerization. Heat and pressure may be employed appropriately to obtain optimal polymerization reaction conditions.

According to yet another· aspect of the invention, the polymerization reactor may comprise a solution polymerization reactor. During solution polymerization, the monomer is contacted with the catalyst composition by suitable stirring or other means. A carrier comprising an inert organic diluent or excess monomer may be employed. If desired, the monomer may be brought in the vapor phase into contact with the catalytic reaction product, in the presence or absence of liquid material. The polymerization zone is maintained at temperatures and pressures that will result

CA 02824482 2013-08-22 in the formation of a solution of the polymer in a reaction medium. Agitation may be employed during polymerization to obtain better temperature control and to maintain uniform polymerization mixtures throughout the polymerization zone.

Adequate means are utilized for dissipating the exothermic heat of polymerization.

The polymerization may be effected in a batch manner, or in a continuous manner. The reactor may comprise a series of at least one separator that employs high pressure and low pressure to separate the desired polymer.

According to a further aspect of the invention, the polymerization reactor system may comprise the combination of two or more reactors. Production of 10 polymers in multiple reactors may include several stages in at least two separate polymerization reactors interconnected by a transfer device making it possible to transfer the polymers resulting from the first polymerization reactor into the second reactor. The desired polymerization conditions in one of the reactors may be different from the operating conditions of the other reactors. Alternatively, 15 polymerization in multiple reactors may include the manual transfer of polymer from one reactor to subsequent reactors for continued polymerization. Such reactors may include any combination including, but not limited to, multiple loop reactors, multiple gas reactors, a combination of loop and gas reactors, a combination of autoclave reactors or solution reactors with gas or loop reactors, multiple solution ( 20 reactors, or multiple autoclave reactors.

After the polymer is produced, it may be formed into various articles, including but not limited to, household containers, utensils, film products, drums, fuel tanks, pipes, geomembranes, and liners. Various processes may be used to form these articles. Usually, additives and modifiers are added to the polymer in order to 25 provide desired effects. By using the invention described herein, articles can likely be produced at a lower cost, while maintaining most or all of the unique properties of polymers produced with metallocene catalysts.

E. Pipe Extrusion

According to one aspect, a method of making a PE-100 pipe is encompassed 30 by the present invention, the method comprising extruding the polymer or copolymer in a molten state through a die to form the PE-100 pipe and cooling the pipe.

CA 02824482 2013-08-22

According to yet other aspects, a PE-100 pipe comprising the polymer or copolymer of the present invention is contemplated.

Pipe extrusion in the simplest terms is performed by melting, conveying polyethylene pellets into a particular shape (generally an annular shape), and solidifying that shape during a cooling process. There are numerous steps to pipe extrusion as provided below.

The polymer feedstock can either be a pre-pigmented polyethylene resin or it can be a mixture of natural polyethylene and color concentrate (referred to as “Salt and Pepper blends”). In North American, the most common feedstock for pipe extrusion is “Salt and Pepper blends”. In Europe and other areas of the world, the most common feedstock for pipe extrusion is pre-pigmented polyethylene resin. Feedstock is rigidly controlled to obtain the proper finished product (pipe) and ultimate consumer specifications.

The feedstock is then fed into an extruder. The most common extruder system for pipe production is a single-screw extruder. The purpose of the extruder is to melt, convey and homogenize the polyethylene pellets. Extrusion temperatures typically range from 178°C to 232°C depending upon the extruder screw design and flow properties of the polyethylene.

The molten polymer is then passed through a die. The die distributes the homogenous polyethylene polymer melt around a solid mandrel, which forms it into an annular shape. Adjustments can be made at the die exit to try to compensate for polymer sag through the rest of the process.

In order for the pipe to meet the proper dimensional parameters, the pipe is then sized. There are two methods for sizing: vacuum or pressure. Both employ different techniques and different equipment.

Next, the pipe is cooled and solidified in the desired dimensions. Cooling is accomplished by the use of several water tanks where the outside pipe is either submerged or water is sprayed on the pipe exterior. The pipe is cooled from the outside surface to the inside surface. The interior wall and inside surfaces of the pipe can stay very hot for a long period of time, as polyethylene is a poor conductor of heat.

CA 02824482 2013-08-22

Finally, the pipe is printed and either coiled or cut to length.

The present invention is further illustrated by the following examples, which are not to be construed in any way as imposing limitations upon the scope thereof. The scope of the claims should not be limited by the preferred embodiments set forth in the description, but should be given the broadest interpretation consistent with the description as a whole.

EXAMPLES

For each of the following examples, testing procedures were as follows.

Melt index (MI, g/10 min) was determined in accordance with ASTM D1238 condition F at 190°C with a 2,160 gram weight.

High load melt index (HLMI, g/10 min) was determined in accordance with ASTM D1238 condition E at 190°C with a 21,600 gram weight.

Polymer density was determined in grams per cubic centimeter (g/cc) on a compression molded sample, cooled at about 15°C per hour, and conditioned for about 40 hours at room temperature in accordance with ASTM D1505 and ASTM D1928, procedure C.

Melt rheological characterizations were performed as follows. Small-strain (10%) oscillatory shear measurements were performed on a Rheometrics Scientific, Inc. ARES rheometer using parallel-plate geometry. All rheological tests were performed at 190°C The complex viscosity |η* j versus frequency (ω) data were then curve fitted using the modified three parameter Carrie-Yasuda (CY) empirical model to obtain the zero shear viscosity - ηο, characteristic viscous relaxation time - τη, and the breadth parameter - a. The simplified YasudaYasuda (CY) empirical model is as follows.

I ?7 * (^) ! —--—____ wherein: |η*(ω)|= magnitude of complex shear viscosity;

ηο = zero shear viscosity;

CA 02824482 2015-01-26 τ1} = viscous relaxation time;

a = “breadth” parameter;

?i = fixes the final power lav/ slope, fixed at 2/11; and ω = angular frequency of oscillatory shearing deformation.

Details of the significance and interpretation of the CY model and derived parameters may be found in: C. A. Hieber and Η. H. Chiang, Rheol. Ada, 28, 321 (1989); C.A. Hieber and H.H. Chiang, Polym. Eng. Sci., 32, 931 (1992); and R. B. Bird, R. C. Armstrong and 0. Hasseger, Dynamics of Polymeric Liquids, Volume I, Fluid Mechanics, 2nd Edition, John Wiley & Sons (1987); each of which is incorporated herein by reference in its entirety. The CY “a” parameter is reported in the tables for the resins disclosed herein.

TM '

A “Quantachrome Autosorb-6 JNitrogen Pore Size Distribution Instrument” was used to determined specific surface area (“surface area”) and specific pore volume (“pore volume”). This instrument was acquired from the Quantachrome

Corporation, Syosset, N.Y.

Molecular weights and molecular weight distributions were obtained using a PL 220 SEC high temperature chromatography unit (Polymer Laboratories) with trichlorobenzene (TCB) as the solvent, with a flow rate of 1 mL/minute at a temperature of 145°C. BHT (2,6-di-tert-butyl-4-methylphenol) at a concentration of

0.5 g/L was used as a stabilizer in the TCB. An injection volume of 200 |1L was used with a nominal polymer concentration of 1.5 mg/mL. Dissolution of the sample in stabilized TCB was carried out by heating at 150°C for 5 hours with TM occasional, gentle agitation. The columns used were three PLgel Mixed A LS columns (7.8x300mm) and were calibrated with a broad linear polyethylene standard (Phillips Marlex® BHB 5003) for which the molecular weight had been determined.

Molecular weight distributions and branch profiles were obtained through size exclusion chromatography using an FTIR detector. Chromato graphic conditions are those described above. However, the sample injection volume was 500 μι. Samples were introduced to the FTIR detector via a heated transfer line and flow cell (KBr windows, 1 mm optical path, and ca. 70 pL cell volume). The temperatures of

CA 02824482 2013-08-22 the transfer line and flow cell were kept at 143 + 1°C and 140 + 1°C, respectively.

Perkin Elmer FTIR spectrophotometer (PE 2000) equipped with a narrow band mercury cadmium telluride (MCT) detector was used in these studies.

All spectra were acquired using Perkin Elmer Timebase software. Background spectra of the TCB solvent were obtained prior to each nm, All IR spectra were measured at 8 cm1 resolution (16 scans). Chromatograms were generated using the root mean square absorbance over the 3000-2700 cm1 spectral region (i.e., FTIR serves as a concentration detector). Molecular weight calculations were made as previously described using a broad molecular weight polyethylene (PE) standard [see Jordens K, Wilkes GL, Janzen J, Rohlfing DC, Welch MB. Polymer 2000-,41:7175]. Spectra from individual time slices of the chromatogram are subsequently analyzed for comonomer branch levels using chemometric techniques. All calibration spectra were taken at sample concentrations which far exceeded that needed for good signal to noise (i.e., > 0.08 mg /mL at the detector).

Branching determination was made as follows. Narrow molecular weight -1.1 tol.3), solvent gradient fractions of ethylene 1-butene, ethylene 1hexene, polyethylene homopolymers, and low molecular weight alkanes were used· in calibration and verification studies. The total methyl content of these samples ranged from 1.4 to 82.7 methyls per 1000 total carbons. Methyl content of samples was calculated from Mn or measured using C-13 NMR spectroscopy. C-13 NMR spectra were obtained on 15 wt. % samples in TCB using a 500 MHz Varian Unity Spectometer run at 125°C as previous described [see Randall JC, Hsieh ET, NMR and Macromolecules; Sequence, Dynamic, and Domain Structure, ACS Symposium Series 247, J. C. Randall, Ed., American Chemical Society, Washington DC, 1984.]. Methyl content per 1000 carbons by NMR was obtained by multiplying (X 1000) the ratio of total methyl signals to total signal intensity.

A partial least squares (PLS) calibration curve was generated using Pirouette chemometric software (Infometrix) to correlate changes in the FTIR absorption spectra with calculated or NMR measured values for methyls/1000 total carbons for the 25 samples. The FTIR absorption spectra used in the calibration model were made from co-added spectra collected across the whole sample. Only a portion of

CA 02824482 2013-08-22 the spectral region (2996 and 2836 cm’1) was used in the calibration step in order to minimize the effects of residual solvent absorption. Preprocessing of spectral data included area normalization, taking the first derivative of the spectra and mean centering all data.

A four component calibration model was calculated and optimized using the process of cross validation (RSQ=0.999, SEV=0.7). The calibration model was verified using 23 additional samples, The predicted versus actual values for the validation data showed excellent correlation (RSQ=0.987) and exhibited a root mean (

square error of prediction equal to +/- 0.4 methyl groups per 1000 total carbon molecules.

Short chain branching levels were calculated by subtracting out methyl chain end contributions. The amount of methyl chain ends were calculated using the equation Mece=C(2-Vce)/M, where Me^ is the number of methyl chain ends per 1000 total carbon molecules, C is a constant equal to 14000, Vee is the number of vinyl terminated chain ends (1 for chromium catalyzed resins), and M is the molecular weight calculated for a particular slice of the molecular weight distribution.

PENT slow crack growth resistance values were obtained at 80°C (1.76°F) according to ASTM F1473 (2001), with the exception that the initial load was 3.8 MPa, in order to accelerate the test. This 3.8 MPa PENT test may be referred to herein as a “high stress” PENT test.

The Charpy testing was the Razor-Notched Room-Temperature Charpy Energy test carried out according to ASTM F2231,

Preparation of Cyclopentadienyl Complexes and Metallocene Compounds

The cyclopentadienyl complexes and metallocenes used in the various examples or described herein were purchased pr prepared as follows. . All manipulations involving air-sensitive reagents and materials were performed under nitrogen by using standard Schlenk line or dry box techniques. The solvent THF was distilled from potassium, while anhydrous diethyl ether, methylene chloride, pentane, and toluene (Fisher Scientific Company) were stored over activated alumina. All solvents were degassed and stored under nitrogen. Zirconium (IV)

CA 02824482 2013-08-22 chloride (99.5%) and n-butyllithium were purchased from Aldrich Chemical

Company and were used as received. Products were analyzed by lH NMR (300

MHz, CDCI3, referenced against residual CHCI3 peak at 7.24 ppm) or 13C NMR (75

MHz, CDC13, referenced against central line of CDCI3 at 77.00 ppm).

Preparation of Sulfated Alumina Activator-Support

Alumina A, from W.R. Grace Company, was impregnated to incipient wetness with an aqueous solution of ammonium sulfate. Typically, the alumina had a surface area of about 330 m2/gram and a pore volume of about 1.3 cc/gram. The amount of ammonium sulfate used was equal to 20% of the starting alumina. The volume of water used to dissolve the ammonium sulfate was calculated from tire total pore volume of the starting sample (i.e. 2.6 mLs of water for each gram of alumina to be treated). Thus, a solution of about 0.08 grams of ammonium sulfate per mL of water was employed. The resulting wêt sand was dried in a vacuum oven overnight at 120 °C, and then screened through a 35 mesh screen. Finally, the material was activated in a fluidizing stream of dry air at 550 °C for 3 hours, in the case of bench scale samples, or 6 hours, for the larger pilot plant samples. The samples were then stored under nitrogen.

EXAMPLE 1

Room Temperature Synthesis ofZrf if-CsHi-tnBu)] CI3

Zr[r]-C5H4-(nBu)]C13 was prepared as described in Example 2, except that the refluxing step was omitted. Instead, the (n-BuCp)2ZrCl2 and ZrCU mixture was stirred at ambient temperature for 20 hrs. FIG. 1 presents the NMR spectrum for the Zr[T|-CsH4-(nBu)]Cl3 formed according to Example 1. The molar ratio obtained for the product Zr[q-C5H4-(nBu)]C13 to starting material (n-BuCp)2ZrCl2 was 1.4:1.

EXAMPLE 2

Inventive Preparation ofZr[^CsHtfnBu)] Cl$

CA 02824482 2013-08-22

A 500 mL Schlenk flask was charged with (n-BuCp)2ZrCl2 (20.0g, 49.4 mmol), ZrCU (12.7g, 54.4 mmol), 300 mL of toluene and a stir bar. The resulting yellow slurry was refluxed under N2 for about 20 h. The dark brown-black reaction mixture was centrifuged to remove excess Z1CI4 and toluene was removed from the filtrate under reduced pressure to obtain a brown-black thick oil. The product was precipitated a couple of times with a CH2Cl2/pentane mixture and vacuum-dried (0.1 mm, 1 h) to afford the desired product as a brown solid. (27 g, 87%). FIG. 2 presents the NMR spectrum for the Zr^-C5H4-(nBu)]Clj formed according to Example 2. The molar ratio obtained for the product Zr^-CsH4-(nBu)]Cl3 to starting material (n-BuCp^ZrCk was 52:1. Thus, the method of making Zr^-CsIL(nBu)]Clj according to the present invention significantly improves the yield and selectivity of the reaction.

EXAMPLE 3

Preparation ofZr[ij-CjHj-fnBu, Me)l,3] CI3

A 500 mL Schlenk flask was charged with (1,3 Me,nBuCp)2ZrCl2 (20.0g, 46.2 mmol), ZrCL (11.9g, 50.7 mmol), 200 mL of toluene and a stir bar. Resulting yellow slurry was refluxed under N2 for about 20 h. Dark brown-black reaction mixture was centrifuged to remove excess ZrCL and toluene was removed from the filtrate under reduced pressure to obtain a brown-black thick oil. The product was precipitated a couple of times with a CH2Cl2/pentane mixture and vacuum-dried (0.1 mm, 1 h) to afford the desired product as a brown solid. (23 g, .76%). *H NMR (CDCI3, δ) 0.94 (t, J = 7.5Hz, Cth), 1.62 -1.31 (m, CH2(CZL)2CH3), 2.44 (s, CH3 ), 2.81-2.75 (m, CH2(CH2)2CH3), 6.24 (broad s, 1, C5H4), 6.45 (broad s, 2, 65¾).

EXAMPLE 4

Preparation of

CA 02824482 2013-08-22

A 500 mL Schlenk flask was charged with nBuCpZrCh (20.0g, 62.7mmol) and approximately 400 mL of diethyl ether. The resulting slurry was cooled to 0°C, after which time (10.7g, 66.0mmol) of Li[(C9He)-l (allyl)] was cannulated as an ethereal solution. The reaction mixture was stirred overnight at ambient temperature and the solvent was removed in vacuo. The resulting solid was dissolved in toluene and centrifuged to remove LiCl. Removal of solvent in vacuo yielded a yellowbrown solid which was dissolved in a dichloromethane/pentane mixture and was cooled to -35°C for a couple of hours. Resulting slurry was filtered, and the precipitate was dried under reduced pressure (0.1 mm, 1 h) to yield the product as a yellow solid (17.0g, 62%). *H NMR (CDC13, δ) 0.87 (t, 7.2Hz, CH3), 1.50-1.22 (m, CH2(CW2)2CH3), 2.58-2.42 (m, C772(CH2)2CH3), 3.77-3.62 (m, CH2=CHCff2), 5.10-5.02 (m, CH>CHCH2), 5.78-5.76 (m, 1, C5H4), 5.87-5.83(m, 2, C5H4)', 5.995.91 (m, CH2=CHCH2), 6.04-6.00 (m, 1, C5H4), 6.39-6.37 (m, 1,0?Η6), 6,63 (d, J=

3.0Hz, 1, C9H6), 7.28-7.18 (m, 2, C9H6), 7.60-7.56(m, 2, C9H6).

CA 02824482 2013-08-22

EXAMPLES

Preparation of Zrtf-CtHrfiCHjhCHs]}{η5

(CH2)2CH=CH2 (H)

A 500 mL Schlenk flask was charged with nBuCpZrCh (5.4g, 17.0mmol) and approximately 150 mL of diethyl ether. The resulting slurry was cooled to 0°C, after which time (3.0g, 17.0mmol) of Li[(C9H6)-l-(butenyl)] was cannulated as an ethereal solution. The reaction mixture was stirred overnight at ambient temperature and the solvent was removed in vacuo. The resulting solid was dissolved in toluene and centrifuged to remove LiCl. Removal of solvent in vacuo yielded a yellowbrown solid which was dissolved in a dichloromethane/peiitane mixture and was cooled to -35°C for a couple of hours. Resulting slurry was filtered, and the precipitate was dried under reduced pressure (0.1 mm, 1 h) to yield the product as a yellow solid (7.2g, 93%). *H NMR (CDC13, δ) 0.79 (t, J= 7.2Hz, CEG), 1.41-1.14 ’ (m, CH2(CH2)2CH3), 2.49-2.19 (m, 4, CH2), 3.07-2.84 (m, CH2)> 4.97-4.84 (m, CH2=CHCH2), 5.65-5.62 (m, 1, €5¾). 5.81-5.68 (m, 3, CH2=C7/CH2, C5H4), 5.955.91(m, 1, C5H4), 6.30-6.29 (m, 1, C9H6), 6.56 (d, 3.3Hz, 1, C9H6), 7.20-7.11 (m, 2, C9H6), 7.53-7.49(m, 2,C9H5).

EXAMPLE 6

Preparation ofZr{fC5H4-[(CH2)^^

(«D

CA 02824482 2013-08-22

A 500 mL Schlenk flask was charged with nBuCpZrCl3 (19.9g, 62.4mmol) and approximately 400 mL of diethyl ether. The resulting slurry was cooled to 0°C, after which time (15.0g, 62.4mmol) of Li[(C9He)-l-(3-phenylpropyl)] was cannulated as an ethereal solution. The reaction mixture was stirred overnight at ambient temperature and the solvent was removed in vacuo. The resulting solid was dissolved in toluene and centrifuged to remove LiCl. Removal of solvent in vacuo yielded a yellow-brown solid which was dissolved in a dichloromethane/pentane mixture and was cooled to -35°C for a couple of hours, Resulting slurry was filtered, and the precipitate was dried under reduced pressure (0.1 mm, 1 h) to yield the product as a yellow solid (23.6g, 73%). NMR (CDCI3, δ) 0.80 (t, 7.2Hz,

1.42-1.15 (m, CH2(C^)2CH3), 1.96-1.84 (m, 2, CH2\ 2.49-2.34 (m, C772(CH2)2CH3), 2.69-2.53 (m, 2, CH2), 3.03-2.80 (m, 2, CH2\ 5.64-5.62 (m, 1, C5H4), 5.75-5.71(m, 2, C5H4), 5.93-5.91 (m, 1, C5H4), 6.31-6.30 (m, 1, C9H6), 6.56 (d, J= 3.3Hz, 1, C9H6), 7.20-7.05 (m, 7, CsHs.CsHs), 7.53-7.46(m, 2, C9H6).

EXAMPLE?

Preparation of

(CHjhCH, (IQ

A 500 mL Schlenk flask was charged with nBuCpZrCl3 (5.4g, 16.8mmol) and approximately 150 mL of diethyl ether. The resulting slurry was cooled to 0°C, after which time (3.0g, 16.8mmol) of Li[(C9H6)-l-(butyl)] was cannulated as an ethereal solution. The reaction mixture was stirred overnight at ambient temperature and the solvent was removed in vacuo. The resulting solid was dissolved in toluene and centrifuged to remove LiCl. Removal of solvent in vacuo yielded a yellow25 brown solid which was dissolved in a dichloromethane/pentane mixture and was cooled to -35°C for a couple of hours. Resulting slurry was filtered, and the

CA 02824482 2013-08-22 precipitate was dried under reduced pressure (0.1 mm, 1 h) to yield the product as a yellow solid (3.7g, 48%). ‘HNMR(CDC13, δ) 0.88-0.78 (m, 6, CH3), 1.58-1.15 (m, 8, W), 2.50-2.35 (m, ŒXCHzhCHj), 2.99-2.73 (m, 2, C%), 5.67-5.64 (m, 1, C5H4), 5.77-5.73(m, 2, C5H4), 5.96-5.92 (m, 1, C5H4), 6.31-6.30 (m, 1, C9H6), 6.56 (d, J= 3.3Hz, 1, C9H7), 7.21-7.09 (m, 2, C9H7), 7.54-7.49(m, 2, C9H7).

EXAMPLE 8 Preparation of Zrtf-CsHr^

A 500 mL Schlenk flask was charged with nBuCpZrCl3 (1.0g, 3.1mmol) and approximately 150 mL of diethyl ether. The resulting sluny was cooled to 0°C, after which time (0.4g, 3.1 mmol) of indenyl lithium was cannulated as an ethereal » solution. The reaction mixture was stirred overnight at ambient temperature and the solvent was removed in vacuo. The resulting solid was dissolved in toluene and centrifuged to remove LiCl. Removal of solvent in vacuo yielded a yellow-brown solid which was dissolved in a dichloromethane/pentane mixture and was cooled to -35°C for a couple of hours. Resulting slurry was filtered, and the precipitate was dried under reduced pressure (0.1 mm, 1 h) to yield the product as a yellow solid (0.8g, 64%). ’H NMR (CDCI3, 5) 0.81 (t, J = 5.0Hz, CH3l 1.43-1.16 (m, CH2(CH3)2CH3), 2.47-2.42 (m, ŒXCH2)2CH3), 5.76 (t, 2.4Hz, 2, C5H4), 5.87 (t, J = 2.4Hz, 2, C5H4), 6.42 (d, J= 3.0Hz, 2, C9H7), 6.82 (t, J= 3.3Hz, 1, C9H7), 7.22-7.16 (m, 2, C9H7), 7.60-7.56 (m, 2, C9H7).

CA 02824482 2015-01-26

EXAMPLE 9

Preparation ofZr[^-CsH3fnBu, Me)l,3] ]}{rf-C9H6-l-(CH2CH^CH2)}Cl2

CHjCH=CH2 (P)

A 500 mL Schlenk flask was charged with (l,3-MeBuCp)ZTCl3 (5.0g, 15.0 mmol) and approximately 150 mL of diethyl ether. The resulting slurry was cooled to 0°C, after which time (2.5g, 15.0 mmol) of LiftCgHg)-! (allyl)] was cannulated as an ethereal solution. The reaction mixture was stirred overnight at ambient temperature and the solvent was removed in vacuo. The resulting solid was dissolved in toluene and centrifuged to remove LiCl. Removal of solvent in vacuo yielded a yellow-brown oily solid which was dissolved in pentane, filtered, and filtrate was cooled to -35°C. Resulting slurry was filtered, and the precipitate was dried under reduced pressure (0.1 mm, 1 h) to yield the product as a yellow, oily solid (3.9g, 57%). *H NMR (CDC13, δ) 0.85-0.77 (m, 6, Œj), 1.46-1.12 (m, 8, CH2(CH2)2CH3), 1.96 (s, CHÙ, 2.04 (s, CH3), 2.49-2.11 (m, 4, C^C^CH^, 3.72-3.53 (m, 4, CH2=CHCtt2), 5.02-4.92 (m, 4, Œz=CHCH2), 5.16 (t, J - 2.7Hz, 1, C5H4), 5.26 (t, J = 2.7Hz, 1, C5H4), 5.74-5.70 (m, 2, C5H4), 5.87-5.82(m, 2, C5H4), 5.80-5.88 (m, CH2=CÆCH2), 6.27-6.25 (m, 2, CgHç), 6.47-6.46 (m, 2, C9H6), 7.19-7.09 (m, 4, C9H6), 7.51-7.44 (m, 4, C9H6).

EXAMPLE 10

Preparation of l-(methyl)-l-(3-butenyl)-l-(cyclopentadienyl)-l-(2,7-di-tertbutylfluorenytymethane zirconiumdichloride l-(Methyl)-l-(3-butenyl)-l-(cyclopentadienyl)-l-(2,7-di-tert-butyIfluorenyl)methane zirconiumdichloride can be prepared using numerous techniques. Several techniques are described in U.S. Patent No. 7,064,225 for

CA 02824482 2015-01-26

IMPROVED SYNTHESIS OF /W^-METALLO CENES AND THEIR PARENT

LIGANDS IN HIGH YIELD, which may be referred to for further details.

Several techniques for preparing the ligand are provided herein by way of example and not by way of limitation. The corresponding ansa-metallocenes that 5 comprise the ligands disclosed herein are prepared in the usual fashion, according to any one of several procedures known in the art, as understood by one of ordinary skill. For example, one procedure to prepare the corresponding zirconium dichloride a/isa-metallocene from these ligands uses 2 equivalents of n-butyllithium (in hexanes) to treat a stirred diethylether solution of the parent ligand, typically at about 10 0°C. Once the n-butyllithium has been added, the ether solution is typically allowed to warm to room temperature overnight, The solution of the dilithiated parent ligand is than added slowly to a slurry of ZrCU in pentane, usually at about 0°C. The solvent is removed in vacuo to afford a solid that can be washed with pentane and extracted with dichloromethane or similar solvents.

a. Preparation of l-(methyl)-l-(3-butenyl)-l-cyclopentadienyl)-l-(2,7di-tert-butylfluorenyl)methane from 2,7-di-tert-butylfluorenyl lithium and 6butenyl-6-methylfulvene

A one-liter flask is charged with 2,7-di-tert-butylfluorene (50 g, 179.6 mmol) 20 and a stir bar, capped with a rubber septum, and placed under a nitrogen atmosphere.

Diethyl ether (about 200 mL) is added via a cannula, and the resulting mixture is cooled to -78°C in a dry-ice bath. This mixture is stirred at this temperature as nbutyllithium (19.0 mL of 10 M in hexanes, 190 mmol) is added slowly via syringe. After the addition of n-butyllithium is complete, the reddish solution is slowly 25 wanned to room temperature and stirred overnight (at least about 12 hours). After this time, the reaction mixture is cooled to -78°C, and 6-butenyl-6-methylfulvene (40 mL) is added quickly (in less than 1 minute) at this temperature with stirring. Upon completion of the fulvene addition, the mixture is removed from the dry ice bath and warmed to room temperature, and a GC aliquot is taken after ca. 15 minutes 3 0 following removal of the dry-ice bath.

Stirring is continued for 7 hours, after which time the reaction mixture is quenched with a saturated NH4CI/H2O solution (300 mL). The organic layer is

CA 02824482 2013-08-22 extracted with diethyl ether, washed twice with H2O (500 mL), dried over anhydrous NaaSCU, filtered, and the filtrate evaporated to dryness to afford a solid. Methanol (ca. 500 mL) is added to the solid and the mixture stirred overnight to form the product as a finely divided white solid. After filtration, washing with MeOH, and drying overnight, the desired parent ligand l-(methyl)-l-(3-butenyl)-l(cyclopentadienyl)-l-(2,7-di-tert-butylfluorenyl)methane is isolated and may be used without further purification.

b. Preparation of l-(methyl)~l-(3-butenyl)-l-(cyclopentadienyl)-l-(2,7di-tert-butylfiuorenyl)methane - Method Al

A one-liter flask is charged with 2,7-di-tert-butylfluorene (50 g, 179.6 mmol) and a stir bar, capped with a rubber septum, and placed under a nitrogen atmosphere. Diethyl ether (about 300 mL) is added via a cannula, and the resulting mixture is cooled to -78°C in a dry-ice bath. This mixture is stirred at this temperature as nbutyllithium (21.5 mL of 10 M in hexanes, 215 mmol) is added slowly via syringe. After the addition of n-butyllithium is complete, the reddish solution is slowly wanned to room temperature and stirred overnight (at least about 12 hours), to provide an ether solution of 2,7-di-fe^butyIfluorenyl lithium. · - Another one-liter flask fitted with an. addition funnel is charged with 6butenyl-6-methylfulvene (37 g, 253 mmol) and a stir bar, and cooled to 0°C under a nitrogen atmosphere. The ether solution of 2,7-di-terfrbutylfluorenyl lithium prepared as above is added in a dropwise fashion to the fulvene at 0°C via the addition funnel over the course of approximately one hour. The resulting darkcolored reaction mixture is wanned to room temperature and stirred overnight (at least about 12 hours) under a nitrogen atmosphere. The reaction mixture is then quenched with the slow addition of a saturated NH4CI/H2O solution (300 mL), the organic layer extracted with ether, washed twice with H2O (500 mL), dried over anhydrous Na2SO4, filtered, and the filtrate evaporated to dryness. The crude product obtained by this method is then dissolved in pentane and maintained at about 0°C in a freezer, thereby affording the product as a white solid that is washed with cold pentane, dried under vacuum, and isolated and used without further

CA 02824482 2013-08-22 purification. Further product could be isolated in smaller quantities through concentrating the mother liquors and combined washings and placing them back in freezer.

c. Preparation of l~(methyl)-l~(3-butenyl)~l-(cyclopentadienyl)-l-(2,7di-iert-butylfluorenyl)methane - Method Â2

An ether solution of 2,7-di-teri-butylfluorenyl lithium is prepared and added in a dropwise fashion over the course of approximately one hour to neat 6-butenyl-6methylftilvene (at 0°C) in the same manner as in Method Al. The resulting reaction mixture is then warmed to room temperature and stirred for 2 days under a nitrogen atmosphere. After this time, an additional 5 mL of 6-butenyl-6-methylfulvene and an additional 30 mL of the zt-butyllithium solution are added to the reaction mixture at room temperature. This mixture is stirred overnight at room temperature.

The reaction mixture is then quenched with the slow addition of a saturated NH4CI/H2O solution (300 mL), the organic layer extracted with ether, washed twice with HjO (500 mL), dried over anhydrous Na2SO4, filtered, and the filtrate evaporated to dryness. The crude product obtained by this method is dissolved in and crystallized from a pentane:Et2O solution (4:1 mixture by volume) at about 0°C, thereby affording the product as a white solid.

d. Preparation of l-(methyl)-l-(3-biitenyl)-l-(cyclopentadienyl)-l-(2,7di-tert~butylfluorenyl)methane—Method A3

A THF solution of 2,7-di-teri-butyIfluorenyl lithium is prepared and added in a dropwise fashion over the course of approximately one hour to the 6-butenyl-6methylfulvene solution (at 0°C) in the same manner as disclosed in Method Al. The resulting dark-colored reaction mixture is warmed to room temperature and stirred overnight (at least about 12 hours) under a nitrogen atmosphere. This THF reaction mixture is then quenched with the slow addition of a saturated NH4CI/H2O solution (300 mL), the organic layer extracted with diethyl ether, washed twice with H2O (500 mL), dried over anhydrous NaaSO^ filtered, and the filtrate evaporated to dryness. The crude product obtained by this method is then dissolved in and crystallized from pentane at about 0°C, thereby affording a product as a white solid.

CA 02824482 2013-08-22

EXAMPLE 11

Preparation of l~(phenyl)-l-(butenyl)-l-(cyclopentadienyl)-l-(2,7-di-tertbutylfluorenyl) methane zirconiumdichloride

A 1 L round bottomed flask is charged with fluorene (23.2 g, 139.6 mmol), THF (400 mL), and a stir bar, and is cooled to -78 °C as n-butyllithium (165 mmol) is slowly added. The mixture is warmed to room temperature, stirred overnight, cooled to 0°C, and 6-phenyl-6-(5-butenyl)fulvene (38 g, 171 mmol), dissolved in 10 THF, added via cannula. After stirring for two days at room temperature the reaction is quenched with saturated NH4CI solution, the organic material extracted with diethyl ether, and the extracts dried over anhydrous Na2SO4< Upon solvent ' removal, a yellow oil is isolated. Chromotography of this oil through silica using heptane affords the desired ligand that may be used without further purification.

EXAMPLE 12

Comparison of Inventive Catalysts with IndjZrCh

Various polymerization runs were conducted to demonstrate the support activity of various metallocenes of die present invention compared with the support 20 activity of bis-indenyl zirconiumdichloride (obtained from Witco under the trade name Eurecen 5032).

All laboratory polymerization runs were conducted in a one-gallon (3.785 liter) stainless steel reactor. The reactor employed an air-operated stirrer with a three bladed propeller and was set to run at 1180 rpm for the duration of a run. The 25 reactor was also encased in a steel jacket with supply lines leading to a heat exchange unit, that was in turn connected to cooling water and a steam line, allowing for temperature control.

The initiation of the charging sequence to the reactor was through an opened charge port while venting with isobutane vapor. An alkylaluminum was injected, 30 quickly followed by addition of the solid activator and catalyst solution. The charge port was closed and 20 psi isobutane vapor added. A side vessel was utilized to hold a measured amount of hexene and this was pushed into the reactor with two liters of

CA 02824482 2013-08-22 isobutane liquid backed by nitrogen pressure. The contents of the reactor were stirred and heated to 2 degrees Centigrade below the desired run temperature, and ethylene was then introduced. A mass flow unit allowed the pressure to climb quickly to 5 psi below the required run pressure, and allowed the smooth transition of ethylene flow until the specified temperature (90°C) and reactor pressure (450 psi) levels were achieved. The reactor pressure was maintained by addition of ethylene on demand. These temperature and pressure levels were maintained for the duration of the run (30 min). At the completion of the run time the ethylene flow was stopped and the reactor pressure slowly vented off. When the pressure and temperature were safely low enough the reactor was opened and the granular polymer powder collected. Activity was specified as grams of polymer produced per gram of solid activator charged per hour. A summary of the various runs is presented in Table 1.

Table 1.

<td> Run</td><td> Catalyst</td><td> Cat. wt. (mg)</td><td> RjAl (ml)</td><td> Time imin)</td><td> 1Hexene (8)</td><td> Support</td><td> Support (mg)</td><td> Solid PE(g)</td><td> Support Activity Wh)</td><td> MI .(g/10. min)</td><td> HLMI g/10 . min</td>

<td> 12-1</td><td> G</td><td> 1.5</td><td> TNBAL 1</td><td> 30</td><td> 10</td><td> Sulfated Al2O3</td><td> 50</td><td> 227</td><td> 9080</td><td> 0.09</td><td> 2.36</td>

<td> 12-2</td><td> G</td><td> 1.5</td><td> TIBA 1</td><td> 30</td><td> 10</td><td> Sulfated AI2O3</td><td> 50</td><td> 136</td><td> 5440</td><td> 0.05</td><td> 1.5</td>

<td> 12-3</td><td> H</td><td> 1.5</td><td> TIBA 1</td><td> 30</td><td> 10</td><td> Sulfated Al2Oa</td><td> 50</td><td> 177</td><td> 7080</td><td> 0</td><td> 0.87</td>

<td> 12-4</td><td> J</td><td> 1.5</td><td> TNBAL 1</td><td> 30</td><td> 10</td><td> Sulfated A12O3</td><td> 50</td><td> 90</td><td> 3600</td><td> 0.03</td><td> 1.18</td>

<td> 12-5</td><td> J</td><td> 1.5</td><td> TIBA 1 .</td><td> 30</td><td> 10</td><td> Sulfated AI2O3</td><td> 50</td><td> 87</td><td> 3480</td><td> 0.01</td><td> 0.78</td>

<td> 12-6</td><td> K</td><td> 1.5</td><td> TNBAL 1</td><td> 60</td><td> 10</td><td> Sulfated AI2O3</td><td> 50</td><td> 210</td><td> 4200</td><td> 0.09</td><td> 2.02</td>

<td> 12-7</td><td> L</td><td> 3</td><td> TIBA 1</td><td> 30</td><td> 10</td><td> Sulfated A120j</td><td> 100</td><td> 177</td><td> 3540</td><td> 0</td><td> 1.76</td>

<td> 12-8</td><td> P</td><td> 3</td><td> TIBA 1</td><td> 30</td><td> 10</td><td> Sulfated ai2o2</td><td> 100</td><td> 130</td><td> 2600</td><td> 0.01</td><td> 0.56</td>

<td> 12-9</td><td> Ind2ZrCI2</td><td> 3</td><td> TIBA 1</td><td> 30</td><td> 10</td><td> Sulfated AI2O3</td><td> 100</td><td> 219</td><td> 4380</td><td> 0</td><td> I</td>

<td> 12-10</td><td> Ind2ZrCl2</td><td> 2</td><td> TNBAL 1</td><td> 30</td><td> 10</td><td> Sulfated A12O}</td><td> 100</td><td> 175</td><td> 3500</td><td> 0.37</td><td> 6.76</td>

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As shown in Table 1, inventive catalysts G (Runs 12-1 and 12-2) and H (Run 12-3), each having an indenyl with a substituent at the 1-position incorporating a terminal olefin, and a mono-substituted cyclopentadienyl, display from about 25 to about 60% higher polymerization activities (support activity) than Ind2ZrCl2 under similar conditions (Runs 12-9 and 12-10).

Additionally, polymers produced by metallocene compounds G and J, and Ind2ZrCl2 were evaluated using 13C NMR to determine the level of 1-hexene incorporation (Runs 12-11 to 12-15), Ind2ZrCl2 generally is considered to be a poor comonomer incorporating catalyst. The results of the evaluation are presented Table 10 2 and illustrated in FIG. 3. As is evident from the data presented, there is a nearly

50% drop in 1-hexene incorporation in the polymers formed using metallocene compounds G and J compared with the polymer formed using Ind2ZrCl2.

Table 2.

<td> Run</td><td> Catalyst</td><td> Cat. Wt (mg)</td><td> 1-Hexene (g)</td><td> RjAl (mL)</td><td> Support</td><td> Support (mg)</td><td> Solid PB (B)</td><td> MI (g/10 min)</td><td> HLMI (g/10 min)</td><td> 1-Hexene (butyl mole %)</td>

<td> 12-11</td><td> Ind2ZrC12</td><td> 1.5</td><td> 10</td><td> TIBA</td><td> Sulfated A12O3</td><td> 50</td><td> 101</td><td> 0.04,</td><td> 3.32</td><td> . 0-.13</td>

<td> 12-12</td><td> G</td><td> 1.5</td><td> 10</td><td> TIBA</td><td> Sulfated A12O3</td><td> 50</td><td> 117</td><td> 0.09</td><td> 2.24</td><td> 0.08</td>

<td> 12-13</td><td> J</td><td> 3.0</td><td> 10</td><td> TIBA</td><td> Sulfated A12O3</td><td> 100</td><td> 340</td><td> 0</td><td> 0.88</td><td> 0.066</td>

<td> 12-14</td><td> Ind2ZrC12</td><td> 2.0</td><td> 25</td><td> TIBA</td><td> Sulfated A12O3</td><td> 100</td><td> . 246</td><td> 0.43</td><td> 11.02</td><td> 0.37</td>

<td> 12-15</td><td> J</td><td> 3.0</td><td> 25</td><td> TIBA</td><td> Sulfated A12Oj</td><td> 100</td><td> 258</td><td> 0.20</td><td> 5.47</td><td> 0.19</td>

EXAMPLE 13

Pilot plant polymerizations were conducted to demonstrate the ability to use dual metallocene catalysts systems according to the present invention to form a bimodal polymer. Metallocene compound C was used to form the high molecular weight component and metallocene compound G was used to form the low molecular weight component.

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To prepare a solution of metallocene C, 2.00 g of solid metallocene C, 1(phenyl)-l-(3-butenyl)-l-(cyclopentadienyl)-l-(2,7-di-tert-butyIfluorenyl)metliane zirconium dichloride, was slurried in about 200 mL of hexene-1, followed by addition of 25 grams of neat (93%) triethylaluminum, under nitrogen. This solution was diluted with 100 to 240 grams of n-heptane and transferred to a steel vessel. Isobutane was added to obtain a total of 40 pounds of solution.

To prepare a solution of metallocene G, 2.00 g of solid metallocene G was dissolved in 420 mL of toluene under nitrogen. The solution was transferred to a steel vessel. Isobutane was added to obtain a total of 40 pounds of solution.

Tri-n-butylaluminum (TNBAL) (obtained from Akzo Corporation) was used as a co-catalyst. The TNBAL was obtained as a neat solution and was diluted to 10 weight percent with heptane. The cocatalyst was added in a concentration in a range of from about 8 to about 26 parts per million of the diluent in the polymerization reactor(s). To prevent static buildup in the reactor, a small amount (less than 5 ppm by weight of diluent) of a commercial antistatic agent sold as “Stadis 450” was usually added,

The pilot plant polymerizations were conducted in a 23-gallon slurry loop reactor at a production rate of approximately 25 pounds of polymer per hour. Polymerization runs were carried out under continuous particle form process conditions in a loop reactor (also known as a slurry process) by contacting a metallocene solution, tri-n-butylaluminum, and a solid activator in a 300 mL stirred autoclave with continuous output to the loop reactor.

The precontacting was carried out in the following maimer. Tri-nbutylaluminum solution and metallocene solution were fed as separate streams into a tee upstream of the autoclave where they contacted each, other. The solid activator

CA 02824482 2015-01-26 (sulfated alumina) was flushed with isobutane into a tee between the aforementioned tee and the autoclave, contacting the tri-n-butylaluminum/metallocene mixture just before entering the autoclave. The isobutane flush used to transport the solid activator into the autoclave was set at a rate that would result in a residence time of 5 approximately 25 minutes in the autoclave. The total flow from the autoclave then entered the loop reactor.

Ethylene used was polymerization grade ethylene (obtained from Union Carbide Corporation) which was purified through a column of alumina and activated at 250°C (482°F) in nitrogen. 1-Hexene, when used, was polymerization grade 110 hexene (obtained from Chevron Phillips Chemical Company LP) which was purified by nitrogen purging and storage over 13x molecular sieve activated at 250°C (482°F) in nitrogen. The loop reactor was a liquid full, 15.2 cm diameter, loop reactor, having a volume of 23 gallons (87 liters). Liquid isobutane was used as the diluent. Some hydrogen was added to regulate the molecular weight of the low molecular 15 weight component of the polymer product. The isobutane was polymerization grade isobutane (obtained from Chevron Phillips Chemical, Borger, Tex.) that was farther purified by. distillation and subsequently passed through a column of alumina (activated at 250°C (482°F) in nitrogen).

Reactor conditions included a pressure around 580 psi (4 MPa), and a 20 temperature that was varied from about 90°C (194°F) to about 99°C (210°F). Also, the reactor was operated to have a residence time of about 1 hour. The solid activator was added through a 0.35 cc circulating ball-check feeder and fed to the 300mL autoclave as described above. Catalyst system concentrations in the reactor were within a range of about 1 to 2 parts per million (ppm) of the diluent in the 25 polymerization reactor. Polymer was removed from the reactor at the rate of about . TM lbs per hour and recovered in a flash chamber. A Vulcan dryer was used to dry the polymer under nitrogen at about 60 to about 80°C (about 40 to about 176°F).

Various resins were prepared according to the above procedure. The results of the evaluation are presented in Table 3.

;

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Table 3.

<td> Run</td><td> Metallocene (Ratio)</td><td> H2 (niLb/ hr)</td><td> Pellet HLMI (dg( 10 min)</td><td> Pellet MI (dg/ 10 min)</td><td> Density (pellets) (S^c)</td><td> Mw (X103)</td><td> Mw/ Mn</td><td> Chaipy (J @23 C) notched</td>

As is evident, the resins produced according to the present invention exhibit excellent high impact strength, illustrated by the 23°C notched charpy impact.

FIG. 4 presents the GPC curves for the resins produced in Run 13-1, 13-2, 13-3 and 13-4, demonstrating that a true bimodal molecular weight distribution polymer is obtained from the catalyst compositions of this invention.

In sum, the present invention provides various catalyst compositions, methods for forming a catalyst composition, and resins and pipes formed by using the catalyst compositions. The catalyst composition generally includes two metallocene compounds, an activator, and a cocatalyst. The two metallocene compounds are selected such that the two metallocenes produce polymers having two distinctly different molecular weights. The metallocenes are combined with an activator-support, an organoaluminum compound, and an olefin monomer to produce a polyolefin having a bimodal molecular weight distribution. The resulting polymers have excellent impact strength. The present invention further provides novel metallocene compounds and an improved method of synthesis of halfmetallocene compounds.

While costly aluminoxanes and organoborates are not required by the present invention, they may be used as desired. As demonstrated by the above examples, the use of a tri-catalyst system, such as those described herein, produces polyolefin films having a desirably low haze while maintaining other physical attributes, such as dart impact.

The foregoing description has been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise

CA 02824482 2013-08-22 examples or embodiments disclosed. Obvious modifications or variations are possible in light of the above teachings. The embodiment or embodiments discussed were chosen and described to provide the best illustration of the principles of the invention and its practical application to enable one of ordinary skill in the art to utilize the invention in various embodiments and with various modifications as are suited to the particular use contemplated. The scope of the claims should not be limited by the preferred embodiments set forth in the description, but should be given the broadest interpretation consistent with the description as a whole.

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Abstract

Term

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METHOD FOR PEPARING MONOCYCLOPENTADIENYL COMPOUNDS

TECHNICAL FIELD OF THE INVENTION

BACKGROUND OF THE INVENTION

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SUMMARY OF THE INVENTION

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BRIEF DESCRIPTION OF THE FIGURES

DEFINITIONS

DETAILED DESCRIPTION OF THE INVENTION

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EXAMPLES

TM '

EXAMPLE 1

EXAMPLE 2

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EXAMPLE 3

EXAMPLE 4

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EXAMPLES

EXAMPLE 6

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EXAMPLE 9

EXAMPLE 10

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EXAMPLE 11

EXAMPLE 12

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EXAMPLE 13

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Classification