AU4743090A - Magnesium oxide-supported ziegler catalyst modified with acid and higher alkanol, and process for preparing narrow mwd hdpe - Google Patents
Magnesium oxide-supported ziegler catalyst modified with acid and higher alkanol, and process for preparing narrow mwd hdpeInfo
- Publication number
- AU4743090A AU4743090A AU47430/90A AU4743090A AU4743090A AU 4743090 A AU4743090 A AU 4743090A AU 47430/90 A AU47430/90 A AU 47430/90A AU 4743090 A AU4743090 A AU 4743090A AU 4743090 A AU4743090 A AU 4743090A
- Authority
- AU
- Australia
- Prior art keywords
- acid
- catalyst
- magnesium oxide
- alkanol
- carboxylic acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/02—Ethene
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
MAGNESIUM OXIDE-SUPPORTED ZIEGLER CATALYST MODIFIED
WITH ACID AND HIGHER ALKANOL, AND PROCESS FOR
PREPARING NARROW MWD HDPE
BACKGROUND OF THE INVENTION High density ethylene homopolymers and copolymers (HDPE) with higher olefins are widely used in injection molding operations. Advantageously such resins should have a narrow molecular weight distribution (MWD) which is largely determined by the nature of the catalyst. The catalyst should also exhibit other desirable characteristics for commercial use. For example, the productivity of the catalyst should be as high as possible so that the resin will have a high ratio of polymer to catalyst residue. It is also very desirable that the catalyst result in a polymer having a large particle size, an advantage vrtiich is particularly sought in gas-phase polymerization. Another desirable characteristic of the catalyst is that it have a hydrogen response. A high hydrogen response means that small increases in the amount of hydrogen used in the reactor (to control molecular weight in the known manner) will result in substantial decrease in molecular weight and a higher melt index polymer. The need for excessive amounts of hydrogen decreases the reactor volume available for the ethylene and other comonomers, thereby reducing productivity.
My U.S. Patent 4,167,493 discloses the treatment of magnesium oxide with methanol, a Lewis base, prior to impregnation with a titanium compound and an aluminum compound to form a Ziegler catalyst vrtiich produces high density polyethylene with a narrow MWD suitable for injection molding.
The production of narrow MWD high density polyethylene using a magnesium oxide supported catalyst is also disclosed in my U.S. Patent 4,288,578 . The catalyst in this patent is made by impregnating a magnesium oxide support with a mixture of titanium
tetrachloride and tetrabutyltitanate and then an organoaluminum compound reducing agent.
In accordance with this invention, a MgO supported catalyst is treated with an organic acid (a Lewis acid), then with the product of TiCl, and a higher alkanol, and finally with an organoaluminum compound as a reducing agent. The catalyst is particularly suitable for preparing HDPE with narrow MWD and large particle size, excellent productivity and hydrogen response.
Magnesium oxide is treated with an organic acid, then with the product of 0.5 to 1.5 moles of an alkanol and one mole of
TiCl., and finally with an organoaluminum compound as a reducing agent.
The catalyst is used in the polymerization of ethylene polymers and copolymers, particularly HDPE, having narrow MWD and large particle size.
The initial treatment of the MgO support with the organic acid is conducted with a molar excess of MgO. Preferably, the ratio of the organic acid to MgO is from 0.001 to 0.5, most preferably from 0.005 to 0.1. The organic acid is desirably an aliphatic mono-carboxylic acid, an aromatic mono-carboxylic acid, an aliphatic dicarboxylic acid, or an aromatic dicarboxylic acid.
Suitable aliphatic mono-carboxylic acids have the formula R-C00H, vrtierein R is H, an alkyl group of 1 to 17 carbon atoms, or a substituted alkyl group of 1 to 17 carbon atoms, such as formic, acetic, propionic, butyric, valeric, caproic, caprylic, capric, lauric, myristic, palmitic or stearic acid, preferably formic, acetic or propionic acid, and most preferably acetic acid.
Suitable aromatic mono-carboxylic acids are benzoic and alkyl- or alkoxy-substituted benzoic acids, such as o-toluic, m-toluic, p-toluic, o-methoxybenzoic, m-methoxybenzoic, p-methoxybenzoic, o-ethoxybenzoic, m-ethoxybenzoic or p-ethoxybenzoic acids (the latter three also known as 1-, 2- or 3-ethoxybenzoic acids, respectively), preferably o-ethoxybenzoic,
p-ethoxybenzoic or m-ethoxybenzoic, and most preferably p-ethoxybenzoic acid.
Suitable aliphatic dicarboxylic acids are oxalic, malonic, succinic, glutaric, adipic, maleic and fu aric acids. Suitable aromatic dicarboxylic acids are phthalic, isophthalic and terephthalic acids.
The acid is typically dissolved in an inert organic solvent, such as hexane, in which the MgO is refluxed.
After drying, the acid-treated MgO support is again treated in a similar manner with the product of an alkanol or polyhydroxy alkanol having 5 to 12 carbon atoms and TiCl. in a ratio of 0.5 to 1.5, preferably 0.8 to 1.2, moles of the alkanol per mole of TiCl4.
After washing and drying, the treated MgO-based catalyst precursor is activated with an organoaluminum compound in the known manner. Particularly suitable aluminum compounds have the formula Rn A"*"X(3-n) n w^cn R *s alkyl, alkenyl, alkylaryl or arylalkyl having 1 to 20 carbon atoms, X is hydrogen or halogen and n is 1, 2 or 3. Compounds in which R is alkyl of 1 to 6 carbon atoms are preferred. Ethylene can be homopolymerized or copolymerized with higher olefins using the catalysts prepared according to the present invention, by any suitable process. Such processes include polymerizations carried out in suspension, in solution or in the gas phase. Gas phase polymerization reactions are preferred, such as those conducted in stirred bed reactors and, especially, fluidized bed reactors.
The molecular weight of the polymer is controlled in the known manner, by using hydrogen. With the catalysts produced according to the present invention, molecular weight may be suitably controlled with hydrogen when the polymerization is carried out at relatively low temperatures, e.g., from 30 to 105°C. This control of molecular weight may be evidenced by a measurable positive change in melt index (I2) of the polymer produced.
The molecular weight distribution (MWD) of the polymers prepared with the catalysts of this invention, as expressed by the melt flow ratio (MFR) values (^j/^)* varies from about 20 to about 32, preferably 21 to 29, for HDPE products with a density of 0.940 to 0.965 g/cc. As recognized by those skilled in the art, such MFR values are indicative of a relatively narrow molecular weight distribution of the polymer. As is also known to those skilled in the art, such MFR values are indicative of the polymers especially suitable for injection molding applications since the polymers having such MFR values exhibit relatively low amounts of warpage and shrinkage on cooling of the injection molded products. The catalysts prepared according to the present invention are highly active and typically have activity of 1,000-5,000 grams of polymer per gram of catalyst per 830 kPa (120 psi) of ethylene per hour.
The linear polyethylene polymers prepared in accordance with the present invention may be homopolymers of ethylene or copoly ers of ethylene with one or more C,-C,Q alpha-olefins. Thus, copolymers having two monomeric units are possible as well as terpolymers having three monomeric units. Particular examples of such polymers include ethylene/1-butene copolymers, ethylene/1-hexene copolymers, etylene/1-octene copolymers, ethylene/4-methyl-1-pentene copolymers, ethylene/1-butene/l-hexene terpolymers, ethylene/propylene/1-hexene terpolymers and ethylene/propylene/1-butene terpolymers. When propylene is employed as a comonomer, the resulting linear low density polyethylene polymer preferably has at least one other alpha-olefin comonomer having at least four carbon atoms in an amount of at least 1 percent by weight of the polymer. The most preferred comonomer is 1-hexene. A commercially significant advantage of the catalysts of this invention is that of producing polymer particles of a relatively large size over 200 microns and usually over 300 microns.
A particularly desirable method for producing polyethylene polymers and copolymers according to the present invention is in a fluid bed reactor. Such a reactor and means for operating it are described by Levine et al, U.S. Patent No. 4,011,382, Karol et al, U.S. Patent No. 4,302,566, and by Nowlin et al, U.S. Patent 4,481,301.
The invention is illustrated by the following non-limiting examples in which all parts are by weight unless otherwise specified.
EXAMPLE 1 (Use of an Aliphatic Carboxylic Acid in Catalyst Synthesis) A sample of MgO support (Merc -Maglite D) was dried in a 500-ml 3-neck flask under nitrogen at 250°C for 16 hours without stirring. 30.8 grams of this dry MgO support was then slurried in 200 ml of dry hexane in a 500-ml 3-neck flask and refluxed for 16 hours with 0.44 ml glacial acetic acid (99.81 pure acetic acid) at 0.01 molar ratio of the acid to the MgO. A dilute pentanol solution was prepared by adding 53.5 ml of pre-dried 1-pentanol (0.494 mole) to 45 ml of dry hexane in another flask. To avoid a rapid isotherm, 54.4 ml of neat TiCl4 (0.494 mole) was added dropwise to the 1-pentanol solution to form the titanium compound solution. The (1:1 pentanol/TiCl4) solution was immediately added to the acetic acid-treated O at room temperature. The slurry was refluxed at 70°C for 16 hours and allowed to cool.
The catalyst precursor was washed 6 times with 100 ml of dry hexane. The solid was re-slurried with 200 ml of dry hexane, and 12 ml of 25 wt. % tri-n-hexylaluminum (TNHAL) solution (7.66 mmole TNHAL) was slowly added (3 minutes) to form a catalyst having an Al/Ti ratio of 0.23. The catalyst was dried for 16 hours at 65°C under nitrogen purge, to give a free-flow light brown powder. Elemental analysis indicated that the finished catalyst contained 1.1 mmoles/g of Ti.
EXAMPLE 2 Catalyst Preparation - Wet Method Using Pentanol and Aromatic Acid A 6.8 gram sample of MgO support (Merck-Maglite D) was dried in a 100-ml Schlenk flask under nitrogen at 250°C for 16 hours without stirring. The MgO support was then slurried in 60 ml dry hexane in a 100-ml Schlenk flask and refluxed for 2 hours with 0.26 ml 2-ethoxybenzoic acid (2-EBA) at 0.012-EBA/MgO molar ratio. A dilute pentanol solution was prepared by adding 11.8 ml of pre-dried 1-pentanol (0.109 mole) to 10 ml of dry hexane in another flask. To avoid a rapid isotherm, 12 ml of neat TiCl. (0.109 mole) was added dropwise to the 1-pentanol solution to form the titanium compound solution. The (1:1 pentanol/TiCl.) solution was immediately added to the 2-EBA treated gO at room temperature. The slurry was refluxed at 7C C for 16 hours and allowed to cool. The catalyst precursor was washed six times with 60 ml of dry hexane. The solid was re-slurried with 60ml of dry hexane, and 2.64 ml of 26 wtt tri-n-hexylaluminum (TNHAL) solution (1.636 mmole TNHAL) was slowly added (about three minutes) to form a catalyst having an Al/Ti ratio of 0.25. The catalyst was dried for 16 hours at 70°C under nitrogen purge, to give a free-flow dark brown powder. Elemental analysis indicated that 1.34 mmoles/g of Ti was on the finished catalyst.
EXAMPLE 3 Catalyst Preparation - Total Deposition Method Using Pentanol A 11.9 gram portion of MgO (Merck Maglite D-J824) was dried in a 3-neck-500-ml-round-bottom flask at 250°C for 16 hours. While stirring with an overhead stirrer carrying a blade stirrer, 60 ml of dry hexane was added, 0.5 ml of 2-ethoxybenzoic acid was syringed in, and the slurry was refluxed for 2 hours. In another small Schlenk flask, 2.6 ml 1-pentanol and 10 ml dry hexane were mixed at room temperature, and 2.6 ml TiCl. was added dropwise to avoid a rapid exotheim. The solution was stirred for an additional 45
minutes to ensure complete reaction before it was syringed into the catalyst flask containing the treated MgO slurry. The slurry was refluxed at 70°C for two hours and cooled to room temperature. Then, 4.6 ml (2.85 mmole) of a 0.62 M TNHAL solution in heptane was syringed in while stirring with a magnetic stirrer. The slurry was stirred for an additional hour to ensure completion of this pre-activation. The catalyst was dried under nitrogen purge at 70°C for 16 hours to give a free-flow dark brown powder. Elemental analysis indicated that 1.31 mmole/g of Ti was on the finished catalyst.
EXAMPLE 4 Slurry Polymerization With Example 2 Catalyst A one gallon slurry reactor was purged with nitrogen at 90°C overnight, cooled to room temperature, 1.8 cc of 25 weight I of di-isobutylaluminumhydride-heptane solution was injected into the reactor, and 0.42 gram of the catalyst of Example 2 was transferred to the reactor with 2 liters of hexane. While stirring, the reactor was heated to 90°C, maintained at 90°C, and 5 cc 1-hexene and 930 kPa (135 psi) partial pressure of hydrogen were added to the reactor. Ethylene was fed continuously to the reactor to maintain the ethylene partial pressure at 930 kPa (135 psi) for 80 min. The product was stabilized with 8.5 cc Irganox 1076 solution (500 ppm in hexane) and dried in a vacuum oven for 4 hours. The product was 335 grams of large mean-particle-size (greater than 400 microns), 10.9 I2, 272 I21, 25 MFR and 0.962 (g/cc) density polymer.
EXAMPLE 5
Slurry Polymerization The polymerizations were run at 90°C with 2 liters of polymerization-grade hexane. Approximately 0.4 gram of the catalyst of Example 2 (0.536 mmole Ti) and 1.8 ml di-isobutylaluminumhydride solution (25 wt. % in heptane) as cocatalyst (2.254 mmole Al), 5ml
1-hexene comonomer, and 310 kPa (45 psia) hydrogen were added in this order to the reactor. The polymerization was run at an ethylene partial pressure of 931 kPa (135 psia) to give the HDPE products in Table I. The product was stabilized with 500 ppm Irganox 1076 stabilizer before drying in the vacuum oven for four hours at 65°C. Melt index (I7)» flow index doi)* density, and melt viscosities (V30 and V300) were measured. The results are presented in Table I.
TABLE 1
Example Catalyst Density MI MFR V30** V300*** V30/V3 of Example
Prior Art* 0.944 3.6 28.5 12989 5488 2.3
0.963 12.9 24 3196 2135 1.5
* U.S. Patent 4,303,771, Example 7 in Table III ** V30 is melt viscosity at 30 sec" shear rate *** V300 is melt viscosity at 300 sec" shear rate
EXAMPLE 6 (Slurry Polymerization) In a manner similar to that of Example 5 polymerization was conducted using the catalyst of Example 2 to determine the effect of the catalyst on median particle size of the polymer and the hydrogen response of the catalyst. The polymerization used a 1:1 molar ratio of hydrogen to ethylene. Results are reported in Table 2 which shows that the catalyst of Example 2 made with pentanol gives a high hydrogen response and a large median particle size, both of which are desirable.
TABLE 2
Polymer
Polymer Hydrogen Median
Catalyst Density Response MFR Particle of Example (g/cc) (12) (I2l/l2) Size (microns)
0.966 16.1 26.4 331
EXAMPLE 7 (Slurry Polymerization With Example 1 Catalyst)
In this Example, the catalyst of Example 1 was used to copolymerize ethylene with 1-hexene, in the manner similar to that of Example 6.
The polymerization was conducted in an 8 liter (2 gallon) slurry reactor at 90°C, with 4 liters of polymerization grade hexane. Approximately 0.07 g of the Example 1 catalyst (0.078 mmole Ti) and 3.6 ml of di-isobutylaluminumhydride solution (25 wt. \ in heptane; 4.53 mmole Al), 10 ml of 1-hexene comonomer, and hydrogen were added in this order to the reactor. The polymerization was run at an ethylene partial pressure of 931 kPa (135 psia) to produce the HPDE products. The H- : C molar ratio was maintained at 1:1. The product was stabilized with 500 ppm of Irganox 1076, and then it was dried in the vacuum oven for 4 hrs at 65°C. Melt index (I2), flow index (I?]) an<^ productivities were measured, and the MFR was calculated from the I2 and I-, measurements. The results are summarized in Table 3.
Table 3
The data of Table I indicates that the hydrogen response of the Examples 1 and 2 catalysts (i.e., the melt index of the polymer made with the catalyst at a given H2:C2 molar ratio) and the MFR's of the polymer products produced with the two catalysts are comparable. However, the activity of the Example 1 catalyst, prepared on the acetic acid - modified MgO support, is substantially higher than that of the Example 2 catalyst, prepared on the 2-ethoxybenzoic acid-modified MgO support.
Claims (10)
1. An olefin polymerization coordination-catalyst comprising a titanium component and an organoaluminum compound reducing agent on a magnesium oxide support which has been pre-treated with a molar deficiency of an organic acid with respect to the magnesium oxide support, in which the titanium component is the reaction product of an alkanol having 5 to 12 carbon atoms and TiCl., with the molar ratio of the alkanol to the TiCl4 being
0.5 to 1.5.
2. The catalyst of claim 1 in which the organic acid is an aliphatic mono-carboxylic acid, an aliphatic di-carboxylic acid, an aromatic mono-carboxylic acid or an aromatic di-carboxylic acid.
3. The catalyst of claim 2 in which the aliphatic mono-carboxylic acid has the formula R-C00H, wherein R is H or an alkyl group of 1 to 17 carbon atoms.
4. The catalyst of claim 3 in which the aliphatic mono-carboxylic acid is acetic acid.
5. The catalyst of claim 3 in which the molar ratio of the alkanol to the TiCl4 is 0.8 to 1.2.
6. The catalyst of claim 1 in which the organoaluminum compound has the formula
*_ A1 (3-n) in which R is alkyl, alkenyl, alkylaryl, or arylalkyl having 1 to 20 carbon atoms, X is hydrogen or halogen and n is 1, 2 or 3.
7. The catalyst of claim 1 in which the organoaluminum compound is tri-n-hexylaluminum.
8. The catalyst of claim 2 in which the aliphatic di-carboxylic acid is oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, aleic acid or fumaric acid.
9. The catalyst of claim 2 in which the aromatic mono-carboxylic acid is benzoic acid, an alkyl-substituted benzoic acid or an alkoxy-substituted benzoic acid.
10. A process of polymerizing olefins comprising ethylene with a coordination-catalyst which comprises a titanium component and an organoaluminum compound reducing agent on a magnesium oxide support which has been pre-treated with a molar deficiency of an organic acid, with respect to the magnesium oxide support, in which the titanium component is the reaction product of an alkanol having 5 to 12 carbon atoms and TiCl4, with the molar ratio of the alkanol to the TiCl4 being 0.5 to 1.5.
6207h/0616h
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38920489A | 1989-08-03 | 1989-08-03 | |
| US389204 | 1989-08-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU4743090A true AU4743090A (en) | 1991-03-11 |
Family
ID=23537287
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU47430/90A Abandoned AU4743090A (en) | 1989-08-03 | 1989-08-30 | Magnesium oxide-supported ziegler catalyst modified with acid and higher alkanol, and process for preparing narrow mwd hdpe |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0436672A1 (en) |
| JP (1) | JPH04500830A (en) |
| AU (1) | AU4743090A (en) |
| WO (1) | WO1991002009A1 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5583085A (en) * | 1994-06-13 | 1996-12-10 | W. R. Grace & Co.-Conn. | Preparation of dehydroxylated supports |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1553673A (en) * | 1975-07-30 | 1979-09-26 | Bp Chem Int Ltd | Polymerisation catalyst |
| JPS5441985A (en) * | 1977-09-09 | 1979-04-03 | Mitsui Petrochem Ind Ltd | Polymerization or copolymerization of olefin |
-
1989
- 1989-08-30 JP JP50117190A patent/JPH04500830A/en active Pending
- 1989-08-30 AU AU47430/90A patent/AU4743090A/en not_active Abandoned
- 1989-08-30 EP EP19900901100 patent/EP0436672A1/en not_active Withdrawn
- 1989-08-30 WO PCT/US1989/003738 patent/WO1991002009A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JPH04500830A (en) | 1992-02-13 |
| WO1991002009A1 (en) | 1991-02-21 |
| EP0436672A1 (en) | 1991-07-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5470812A (en) | High activity polyethylene catalysts prepared with alkoxysilane reagents | |
| US4719193A (en) | Processes for preparing polyethylene catalysts by heating catalyst precursors | |
| JP2557054B2 (en) | Alpha-olefin polymerization catalyst composition | |
| US5118648A (en) | Particulate polymer-supported olefin polymerization catalyst | |
| CA2389654C (en) | Polymerization catalyst systems and processes using alkly lithium compounds as a cocatalyst | |
| AU677145B2 (en) | Catalyst composition | |
| US4888318A (en) | Catalyst composition for polymerizing alpha-olefins | |
| JP2774807B2 (en) | Catalyst composition for polymerization of alpha-olefin polymer with narrow molecular weight distribution | |
| CA2296303A1 (en) | Catalyst for the manufacture of polyethylene with a broad or bimodal molecular weight distribution | |
| US6124412A (en) | Alumoxane-enhanced, supported ziegler-natta polymerization catalysts, methods of making same, processes of using same and polymers produced therefrom | |
| EP0729478B1 (en) | A catalyst composition for the copolymerization of ethylene | |
| US5260245A (en) | High activity polyethylene catalysts | |
| US5408015A (en) | Mixed chromium catalyst,and alkene and alkyl aluminum hydride-modified ziegler catalyst for multimodal HDPE | |
| EP0324588A2 (en) | Catalyst composition for polymerizing alpha-olefin polymers of narrow molecular weight distribution | |
| US5994256A (en) | Process for forming a catalyst precursor for copolymerizing ethylene and an alpha-olefin of 3 to 10 carbon atoms | |
| US5055533A (en) | Process for polymerizing alpha-olefins with trimethylaluminum-activated catalyst | |
| IE58840B1 (en) | Process for simultaneously dimerizing ethylene and copolymerizing ethylene with the dimerized product | |
| US5232999A (en) | Olefin polymerization catalyst and process | |
| US6291384B1 (en) | High activity catalyst prepared with alkoxysilanes | |
| US5330950A (en) | Mixed Ziegler and chromium catalyst and process for preparing a broad molecular weight distribution HDPE | |
| JPH0721005B2 (en) | Catalyst composition for (co) polymerization of ethylene | |
| US4863886A (en) | Magnesium oxide-supported ziegler catalyst modified with acid and higher alkanol, and process for preparing narrow MWD HDPE | |
| JP4547124B2 (en) | Catalyst composition for olefin polymerization and process using the composition | |
| AU4743090A (en) | Magnesium oxide-supported ziegler catalyst modified with acid and higher alkanol, and process for preparing narrow mwd hdpe | |
| US5330951A (en) | Catalyst composition for polymerizing alpha-olefin |