Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Polymers from only ethylenic monomers or processes of...
Reexamination Certificate
2002-05-03
2003-11-04
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...
C526S128000, C526S160000, C526S170000, C526S943000, C526S348200, C526S348500, C526S348600
Reexamination Certificate
active
06642326
ABSTRACT:
FIELD OF THE INVENTION
This invention relates to a polymerization process for olefins. In particular, the invention relates to a high activity polymerization process with a boraaryl single-site catalyst precursor, an activator and a silane modifier.
BACKGROUND OF THE INVENTION
Interest in single-site (metallocene and non-metallocene) catalysts continues to grow rapidly in the polyolefin industry. These catalysts are more reactive than Ziegler-Natta catalysts and they produce polymers with improved physical properties. The improved properties include narrow molecular weight distribution, reduced low molecular weight extractables, enhanced incorporation of &agr;-olefin comonomers, lower polymer density, controlled content and distribution of long-chain branching, and modified melt rheology and relaxation characteristics.
Traditional metallocenes commonly include one or more cyclopentadienyl groups, but many other ligands have been used. Thus, a catalyst structure can be fine-tuned to give polymers with desirable properties. A preferred group of polymerization-stable ligands are boraaryl ligands as described in U.S. Pat. Nos. 5,554,775 and 6,355,818.
The incorporation of silanes in polymerizations using cyclopentadienyl metallocene catalysts is described in EP 0739910
, J. Am. Chem. Soc
. 121 (1999) 8791, and in U.S. Pat. Nos. 5,578,690, 6,075,103 and 6,077,919. High levels of silane are used to control the molecular weight. For instance, in the seventeen examples of EP 0739910, the silane is used in amounts of 26,800 to 465,000 ppm Si. At these levels, polymer molecular weight decreases with increasing silane and there is no clear effect on activity.
Despite the importance of olefin polymerizations and the considerable research that has been done on various catalyst systems, there remains a need to improve the activity of the catalyst. This can be important from a cost view since the catalyst is typically one of the more costly ingredients. Similarly, the equipment for catalyst handling can add to the cost. Any improvement in catalyst activity decreases these costs. However, even more important is that the residual metal in the polymer is reduced. High levels of residual metal can have a deleterious effect on polymer properties such as color and aging. It is therefore important to keep the residual metals as low as possible. Any improvement in catalyst activity lowers the residual metals in the polymer.
SUMMARY OF THE INVENTION
This invention is a process for the polymerization of an olefin. An olefin is polymerized with a catalyst precursor in the presence of an activator and a modifier. The modifier is a hydrosilane or a polysiloxyhydrosilane and serves to improve the activity of the catalyst. Low levels of the modifier give a large increase in catalyst activity while still affording high molecular weight polymers. The process of the invention is easy to practice and affords enhanced catalyst activity. Since the catalyst is not removed from the final polymer, an increase in activity results in a polymer with lower residual metals. The process is robust and gives an improvement in activity for copolymers of olefins such as ethylene and propylene as well as the homopolymers.
DETAILED DESCRIPTION OF THE INVENTION
The invention is an olefin polymerization process. Suitable olefins are C
2
-C
20
&agr;-olefins, such as ethylene, propylene, 1-butene, 1-hexene, 1-octene and mixtures thereof. Preferred olefins are ethylene, propylene and mixtures thereof with &agr;-olefins such as 1-butene, 1-hexene and 1-octene.
The polymerization is performed with a catalyst precursor comprising a Group 3 to 10 transition metal, M, and at least one anionic boraaryl ligand. Boraaryl ligands are described in U.S. Pat. Nos. 5,554,775 and 6,355,818, the teachings of which are incorporated herein by reference. In addition to the boraaryl ligand, the catalyst precursor may also include a polymerization-stable anionic ligand. Examples include substituted and unsubstituted cyclopentadienyl, fluorenyl and indenyl, or the like, such as those described in U.S. Pat. Nos. 4,791,180 and 4,752,597, the teachings of which are incorporated herein by reference. Other suitable polymerization-stable ligands are heteroatomic ligands such as pyrrolyl, indolyl, indenoindolyl, quinolinoxy, pyridinoxy, and azaborolinyl as described in U.S. Pat. Nos. 5,539,124, 5,637,660, 5,902,866, and 6,232,260, the teachings of which are incorporated herein by reference. The catalyst precursor also usually includes one or more labile ligands such as halides, alkyls, alkaryls, aryls, dialkylaminos, or the like. Particularly preferred are halides, alkyls, and alkaryls (e.g., chloride, methyl, benzyl). Preferred transition metals are Group 4-6 transition metals, and of these, zirconium is especially preferred.
The catalysts include an activator. Suitable activators ionize the catalyst precursor to produce an active olefin polymerization catalyst. Combinations of activators may be used. Suitable activators are well known in the art. Examples include alumoxanes (methyl alumoxane (MAO), PMAO, ethyl alumoxane, diisobutyl alumoxane), alkylaluminum compounds (triethylaluminum, diethyl aluminum chloride, trimethylaluminum, triisobutyl aluminum), and the like. Suitable activators include acid salts that contain non-nucleophilic anions. These compounds generally consist of bulky ligands attached to boron or aluminum. Examples include lithium tetrakis(pentafluorophenyl)borate, lithium tetrakis (pentafluorophenyl)-aluminate, anilinium tetrakis(pentafluorophenyl)borate, and the like. Suitable activators also include organoboranes, which include boron and one or more alkyl, aryl, or aralkyl groups. Suitable activators include substituted and unsubstituted trialkyl and triarylboranes such as tris(pentafluorophenyl)borane, triphenylborane, tri-n-octylborane, and the like. These and other suitable boron-containing activators are described in U.S. Pat. Nos. 5,153,157, 5,198,401, and 5,241,025, the teachings of which are incorporated herein by reference.
Suitable activators also include aluminoboronates—reaction products of alkyl aluminum compounds and organoboronic acids—as described in U.S. Pat. Nos. 5,414,180 and 5,648,440, the teachings of which are incorporated herein by reference.
The amount of activator needed relative to the amount of catalyst precursor depends on many factors, including the nature of the precursor and activator, the desired reaction rate, the kind of polyolefin product, the reaction conditions, and other factors. Generally, however, when the activator is an alumoxane or an alkyl aluminum compound, the amount used will be within the range of about 0.01 to about 5000 moles, preferably from about 0.1 to about 500 moles, of aluminum per mole of M. When the activator is an organoborane or an ionic borate or aluminate, the amount used will be within the range of about 0.01 to about 5000 moles, preferably from about 0.1 to about 500 moles, of activator per mole of M.
The activator is normally added to the reaction mixture at the start of the polymerization. Optionally, a portion of the activator is premixed with the catalyst and the remainder added directly to the reactor. When a supported catalyst system is used, the activator can be deposited onto the support along with the catalyst precursor.
The catalyst precursor and activator are optionally used with an inorganic solid or organic polymer support. Suitable inorganic supports include silica, alumina, silica-aluminas, magnesia, titania, clays, zeolites, or the like. The inorganic support is preferably treated thermally, chemically, or both prior to use to reduce the concentration of surface hydroxyl groups. Thermal treatment consists of heating (or “calcining”) the support in a dry atmosphere at elevated temperature, preferably greater than about 100° C., and more preferably from about 150° C. to about 600° C., prior to use. A variety of different chemical treatments can be used, including reaction with organo-aluminum, -magnesium, -silicon, or -boron compounds. See, for example, the te
Meyer Karen E.
Reinking Mark K.
Equistar Chemicals LP
Lee Rip A
Schuchardt Jonathan L.
Tyrell John
Wu David W.
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