Ethylene polymerization process

Details Ethylene polymerization process Ethylene polymerization process

2000-06-14

2002-06-11

Wu, David W. (Department: 1713)

Synthetic resins or natural rubbers -- part of the class 520 ser

Synthetic resins

Polymers from only ethylenic monomers or processes of...

C526S134000, C526S943000, C526S941000, C526S348000, C502S104000, C502S114000

Reexamination Certificate

active

06403736

ABSTRACT:

FIELD OF THE INVENTION
The invention relates to ethylene polymerization by single-site catalysts. More particularly, the invention relates to a process that reduces the induction time of the catalyst and produces polyethylene having a high bulk density.
BACKGROUND OF THE INVENTION
Single-site catalysts are known. They can be divided into metallocene and non-metallocene. Metallocene single-site catalysts are transition metal compounds that contain cyclopentadienyl (Cp) or Cp derivative ligands. Non-metallocene single-site catalysts are referred to as those that contain ligands other than Cp but have the same catalytic characteristics as the metallocene. The non-metallocene single-site catalysts usually contain heteroatomic ligands, e.g., boraaryl (see U.S. Pat. No. 6,034,027), pyrrolyl (see U.S. Pat. No. 5,539 ,124), azaborolinyl (see U.S. Pat. No. 5,756,611) and quinolinyl (see. U.S. Pat. No. 5,637,660). Single-site catalysts produce polyethylene of many properties that are not available to those made by Ziegler catalysts, for example, narrow molecular weight distribution and low density.
Successful production of polyethylene with the newly developed single-site catalysts offers many challenges. First, often the catalysts need to be modified for the desired activity and stability. For example. co-pending U.S. application Ser. No. 09/318,009 (U.S. Pat. No. 6,291,386) teaches in-situ alkylation of a single-site catalyst by reacting the catalyst that has at least one labile ligand with alkyl aluminum in the polymerization system. The labile ligand is removed and replaced by the alkyl group resulting in the catalyst having improved stability and activity. However, the in-situ alkylation increases the induction time of the catalyst, i.e., the time needed for the catalyst to start the polymerization.
Furthermore, polyethylene and other olefin polymers made by single-site catalysts are highly desirable if they can be processed in the existing thermal processing equipment. Many thermal processes including blowing film extrusion, injection molding and blow molding require polyethylene to have a relatively high bulk density (usually greater than about 0.30 g/cm
3
). Low bulk density gives a low production rate and also can result in inferior product quality. Bulk density also affects ethylene polymerization. Low bulk density means low productivity per reactor unit. Polyethylene of low bulk density also dries slowly because it absorbs solvent and residual monomers.
One approach to shorten the induction time of the catalyst is to premix the catalyst with alkyl aluminum right before being added into the polymerization system. However, this approach results in a lower bulk density of polyethylene. Very surprisingly, I have found that premixing the catalyst with triethyl aluminum can retain high bulk density of polyethylene while shortening the induction time.
SUMMARY OF THE INVENTION
The invention is an ethylene polymerization process. The process uses a single-site catalyst that contains at least one boraaryl ligand. The process includes supporting the catalyst, premixing the supported catalyst with alkyl aluminum, and polymerizing ethylene in the presence of the catalyst. Premixing the catalyst with alkyl aluminum significantly reduces the induction time of the catalyst.
The invention also includes a process that produces polyethylene of a bulk density greater than about 0.30 g/cm
3
. I have found that premixing the catalyst with triethyl aluminum not only reduces the induction time of the catalyst but also retains or enhances the bulk density of polyethylene.
DETAILED DESCRIPTION OF THE INVENTION
The process of the invention includes supporting a single-site catalyst. The single-site catalyst is a Group 3-10 metal compound that contains at least one boraaryl ligand. Preferably, the metal is titanium, zirconium, or hafnium. Zirconium is particularly preferred. The boraaryl ligand includes substituted or non-substituted borabenzene, boranaphthalene, boraanthracene, and boraphenanthrene. Preferably, the boraaryl ligand is borabenzene or substituted borabenzene, e.g., 1-methylborabenzene. U.S. Pat. Nos. 5,554,775, 5,637,659, and 6,034,027, the teachings of which are herein incorporated by reference, teach how to prepare catalysts that contain a boraaryl ligand.
In addition to a boraaryl ligand, other ligands are used. The total number of ligands satisfies the valence of the transition metal. The ligands can be bridged or non-bridged. Other suitable ligands include substituted or non-substituted cyclopentadienyls, indenyls, fluorenyls, halides, C
1
-C
10
alkyls, C
6
-C
15
aryls, C
7
-C
20
aralkyls, dialkylamino, siloxy, alkoxy, and the like, and mixtures thereof. Cyclopentadienyls and indenyls are preferred.
Suitable ligands also include other heteroatomic ligands such as pyrrolyl, azaborolinyl, and quinolinyl. Methods for preparing heteroatomic ligand-containing single-site catalysts are available in the literature. For example, U.S. Pat. Nos. 5,539,124, 5,756,611, and 5,637,660, the teachings of which are herein incorporated by reference, teach how to make single-site catalysts that contain pyrrolyl, azaborolinyl, and quinolinyl ligands.
Examples of boraaryl-based single-site catalysts are (borabenzene)(cyclopentadienyl)zirconium dichloride, (1-methylborabenzene)(cyclopentadienyl)zirconium dichloride, (borabenzene)(indenyl)zirconium dichloride, (1-methylborabenzene) (indenyl)zirconium dichloride, (boranaphthalene)(cyclopentadienyl)zirconium dichloride, and (boraanthracene)(cyclopentadienyl)zirconium dichloride.
The catalyst is immobilized on a support. The support is preferably a porous material such as inorganic oxides and chlorides, and organic polymer resins. Preferred inorganic oxides include oxides of Group 2, 3, 4, 5, 13, or 14 elements. Preferred supports include silica, alumina, silica-aluminas, magnesias, titania, zirconia, magnesium chloride, and crosslinked polystyrene. Preferably, the support has a surface area in the range of about 10 to about 700 m
2
/g, a pore volume in the range of about 0.1 to about 4.0 mL/g, an average particle size in the range of about 10 to about 500 &mgr;m, and an average pore diameter in the range of about 10 to about 1000 Å. They are preferably modified by heat treatment, chemical modification, or both. For heat treatment, the support is preferably heated at a temperature from about 50° C. to about 800° C. Suitable chemical modifiers include organoaluminum, organosilicon, organomagnesium, and organoboron compounds.
The catalysts are supported using any known techniques. For example, U.S. Pat. Nos. 5,747,404 and 5,744,417, the teachings of which are incorporated herein by reference, teach how to support single-site catalysts onto a polysiloxane or a silylamine polymer. In one suitable method, the single-site catalyst is dissolved in a solvent and combined with the support. Evaporation of the solvent gives a supported catalyst.
The catalyst is used with an activator. Activators can be mixed and supported together with single-site catalysts on a support or added separately to the polymerization reactor. Suitable activators include anionic compounds of boron and aluminum, trialkylboron and triarylboron compounds, and the like. Examples are lithium tetrakis (pentafluorophenyl)borate, triphenylcarbenium tetrakis(pentafluorophenyl)borate, lithium tetrakis(pentafluorophenyl)aluminate, tris(pentafluorophenyl)boron, tris(pentabromophenyl)boron, and the like. Activators are generally used in an amount within the range of about 0.01 to about 100,000, preferably from about 0.1 to about 1,000, and most preferably from about 0.5 to about 300, moles per mole of the single-site catalyst.
The process of the invention includes premixing the supported catalyst with trialkyl aluminum, AlR
3
, where R has 1 to 10 carbons. Examples of suitable alkyl aluminum include trimethyl aluminum (TMA), triethyl aluminum (TEAL) and triisobutyl aluminum (TIBAL). Without the premixing the catalyst with trialkyl aluminum, the catalyst has about eight minutes of induction time,

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