JPH083215A - Method for polymerizing alpha-olefin - Google Patents

Abstract

PURPOSE:To enable the production of an alpha-olefin polymer having high activity, stereoregularity, and melt flowability. CONSTITUTION:An alpha-olefin is polymerized in the presence of a catalyst which comprises a solid catalyst component essentially contg. magnesium, titanium, a halogen, and an electron-donor, an organoaluminum compd., and an organosilicon compd. represented by the general formula: R<1>nSi(OR<2>)3-n, (NR<3>R<4>) [wherein R<1> is a 1-24C aliph. hydrocarbon group or an arom. hydrocarbon group; R'' is a 1-24C hydrocarbon group provided when R<1> is arom., then R<2> is not ethyl; R<3> and R<4> are each a 1-14C hydrocarbon group; and (n) is 0-2].

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention uses a highly active catalyst to obtain α
And a method for polymerizing an olefin to produce an α-olefin polymer having high stereoregularity and high melt fluidity.

[0002]

2. Description of the Related Art In recent years, in order to polymerize .alpha.-olefins, a solid catalyst component which requires magnesium, titanium, a halogen element, and an electron donor as an essential component, and an organometallic group I to III metal. A highly active catalyst system comprising a compound and an electron donor as a third component is disclosed in JP-A-57-633.
Many proposals are made in JP-A No. 10-58, JP-A No. 58-83016, JP-A No. 59-58010, and JP-A No. 60-44507. Further, JP-A-58-83006 and JP-A-63-258907
Japanese Patent Laid-Open No. 4-370103 and the like disclose a polymerization catalyst characterized by using a specific silicate as a third component. Generally, in the case of producing an α-olefin polymer, in order to improve the melt flowability of the polymer, a method of using a chain transfer agent such as hydrogen and increasing the melt flow rate (MFR) of the polymer is used. There is.

However, in the above catalyst system, usually,
When the amount of chain transfer agent such as hydrogen used is increased to improve the melt flowability of the polymer, the boiling heptane-insoluble matter (HI) is generally greatly reduced. Further, since the melt fluidity of the produced polymer has little dependence on the hydrogen usage of the chain transfer agent, it is necessary to use a large amount of hydrogen in order to improve the melt fluidity. Therefore, the various highly active catalysts described in the above publications are said to be excellent catalysts which are highly active and improve the stereoregularity of the polymer, but particularly obtain a polymer having high melt fluidity. In this case, the above-mentioned drawback becomes a big problem, and its solution is desired.

[0004]

SUMMARY OF THE INVENTION The present invention provides a method for producing an α-olefin polymer having high stereoregularity and high melt fluidity by polymerizing an α-olefin using a highly active catalyst.

[0005]

SUMMARY OF THE INVENTION The present invention provides a catalyst solid component containing magnesium, titanium, a halogen element and an electron donor as component [A], an organoaluminum compound component as component [B], and As the component [C], a compound represented by the general formula (I) R ¹ _n Si (OR ² ) _3-n (NR ³ R ⁴ ) (I) (wherein R ¹ is an aliphatic hydrocarbon group having 1 to 24 carbon atoms or an aromatic group) Represents a group hydrocarbon group, R ² represents a hydrocarbon group having 1 to 24 carbon atoms (however, when R ¹ is an aromatic hydrocarbon group, R ² excludes an ethyl group), and R ³ and R ⁴ Represents a hydrocarbon group having 1 to 24 carbon atoms, and n is 0 to 2). An α-olefin is polymerized in the presence of a catalyst consisting of an organosilicon compound represented by A method for polymerizing an olefin is provided.

In the present invention, a solid catalyst component containing magnesium, titanium, a halogen element, and an electron donor as essential components is used as the component [A]. The method for producing the catalyst solid component is not particularly limited, and examples thereof include JP-A-54-94590, JP-A-56-55405, JP-A-56-45909, and JP-A-56-163.
102 publication, 57-63310 publication, 57-115408 publication,
58-83006, 58-83016, 58-138707, 59-149905, 60-23404, 60-3.
The methods proposed in JP 2805, JP 61-18330, JP 61-55104, JP-A-2-77413 and JP 2-117905 can be used. As a typical manufacturing method,
(1) A method of co-milling a magnesium compound such as magnesium chloride, an electron donor, and a titanium halide compound such as TiCl ₄ , (2) a magnesium compound and an electron donor are dissolved in a solvent, and the titanium halide is added to this solution. Examples thereof include a method of adding a compound to deposit a catalyst solid.

As the component [A], the catalyst solid components described in JP-A-60-152511, JP-A-61-31402 and JP-A-62-81405 are particularly preferable for achieving the effect of the present invention. preferable. According to the manufacturing method thereof described, wherein an aluminum halide (wherein, X ¹ is a halogen.) Represented by AlX ¹ ₃ and is represented by the formula _{^{R 4 n Si (OR 5)}} 4-n Silicon compound
(In the formula, R ⁴ and R ⁵ each represent an alkyl group having 1 to 8 carbon atoms or a phenyl group, and n is an integer of 0 to 3.), and R ⁶ MgX ² A magnesium compound represented by the formula (in the formula, R ⁶ represents an alkyl group having 1 to 8 carbon atoms and X ² represents a halogen atom) is reacted to deposit a solid. As the aluminum halide that can be used in the above reaction, anhydrous aluminum halide is preferable, but it is difficult to use completely anhydrous aluminum halide due to hygroscopicity, and aluminum halide containing a small amount of water should also be used. You can Specific examples of aluminum halides include aluminum trichloride, aluminum tribromide and aluminum triiodide, with aluminum trichloride being particularly preferred.

Specific examples of the silicon compound used in the above reaction include tetramethoxysilane, tetraethoxysilane, tetrabutoxysilane, methyltriethoxysilane, ethyltributoxysilane, phenyltrimethoxysilane, phenyltributoxysilane and dimethyl. Diethoxysilane, diphenyldimethoxysilane, methylphenyldimethoxysilane, diphenyldiethoxysilane,
Examples thereof include trimethyl monoethoxysilane and trimethyl monobutoxy silane. In particular, methylphenyldimethoxysilane, tetraethoxysilane, methyltriethoxysilane, phenyltrimethoxysilane and dimethyldiethoxysilane are preferable. The amount of the compound used in the reaction between the aluminum halide and the silicon compound is usually 0.4 to 1.5, preferably 0.7 to, in terms of element ratio (Al / Si).
It is in the range of 1.3, and it is preferable to use an inert solvent such as hexane and toluene in the reaction. The reaction temperature is generally 10 to 100 ° C, preferably 20 to 80 ° C, and the reaction time is generally 0.2 to 5 hours, preferably 0.5 to 3 hours.

Specific examples of the magnesium compound used in the above reaction include ethyl magnesium chloride, propyl magnesium chloride, butyl magnesium chloride, hexyl magnesium chloride, octyl magnesium chloride, ethyl magnesium bromide, propyl magnesium bromide, butyl magnesium bromide and ethyl. Examples include magnesium iodide. As the solvent of the magnesium compound, for example, an aliphatic ether such as diethyl ether, dibutyl ether, diisopropyl ether, diisoamyl ether, or an aliphatic cyclic ether such as tetrahydrofuran can be used.

The amount of the magnesium compound used is usually 0.5 to 3, preferably 1.5 to 2.3 in terms of the element ratio (Mg / Al) to the aluminum halide used in the preparation of the reaction product of the aluminum halide and the silicon compound. It is a range. The reaction temperature is usually -50 to 100 ° C, preferably-
20 to 50 ° C, reaction time is usually 0.2 to 5 hours, preferably
0.5 to 3 hours.

The white solid obtained in the reaction of an aluminum halide with a silicon compound and subsequently with a Grignard compound is contact-treated with an electron donor and a titanium halide compound. As a method of contact treatment,
(1) A method of treating a solid with a titanium halide compound, then treating with an electron donor, and then again treating with a titanium halide compound, and (2) treating the solid with a titanium halide compound and an electron donor. Then, a well-known method such as a method of treating with a titanium halide compound after the treatment with 1 can be adopted. For example, the above solid is dispersed in an inert solvent and the electron donor or / and the titanium halide compound is dissolved therein, or an electron donor or / and a liquid titanium halide compound is used without using an inert solvent. Disperse the solid in. In this case, the contact treatment between the solid and the electron donor or / and the titanium halide compound can be carried out under stirring at a temperature of usually 50 to 150 ° C. and a contact time of 0.2 to 5 hours, although there is no particular limitation. Further, this contact treatment can be performed multiple times.

The titanium halide compound which can be used in the contact treatment is represented by the formula Ti (OR) _p X ³ _4-P (p is an integer of 0 to 3 and X ³ represents a halogen atom). Specific examples include tetrachlorotitanium, tetrabromotitanium, trichloromonobutoxy titanium, tribromomonoethoxy titanium, trichloromonoisopropoxy titanium, dichlorodiethoxy titanium, dichlorodibutoxy titanium, monochlorotriethoxy titanium, monochlorotributoxy titanium. Can be mentioned. Particularly, tetrachlorotitanium and trichloromonobutoxytitanium are preferable.

The electron donor used in the above contact treatment is preferably an aromatic ester, particularly an orthophthalic acid diester. Specific examples of the diester include diethyl orthophthalate, diisobutyl orthophthalate, dipentyl orthophthalate, dihexyl orthophthalate, di-2-ethylhexyl orthophthalate, and di-n-heptyl orthophthalate. After the above-mentioned catalytic treatment, the treated solid is generally separated from the treated mixture and thoroughly washed with an inert solvent, and the obtained solid is used as the catalyst solid component [A] of the present invention as an α-olefin polymerization catalyst. be able to.

As the organoaluminum compound as the component [B] of the present invention, alkylaluminum, halogenoalkylaluminum and the like can be used, but alkylaluminum is preferred. Trialkylaluminum is particularly preferable, and specific examples thereof include trimethylaluminum, triethylaluminum, triisobutylaluminum, trihexylaluminum, trioctylaluminum and the like. Any of the organoaluminum compounds may be used as a mixture. Further, polyaluminoxane obtained by the reaction of alkylaluminum and water can be used as well. The amount of the organoaluminum compound used as the α-olefin polymerization catalyst is 0.1 to 500, preferably 0.5 to 500 in terms of the element ratio (Al / Ti) to titanium of the catalyst solid component [A].
It is 150.

The component [C] of the present invention is represented by the general formula (I) R ¹ _n Si (OR ² ) _3-n (NR ³ R ⁴ ) (I) (wherein R ¹ has 1 to 24 carbon atoms). Represents an aliphatic hydrocarbon group or an aromatic hydrocarbon group, R ² is a hydrocarbon group having 1 to 24 carbon atoms (however, when R ¹ is an aromatic hydrocarbon group, R ² excludes an ethyl group) And R ³ and R ⁴ represent a hydrocarbon group having 1 to 24 carbon atoms, and n is 0 to 2).

A preferred hydrocarbon group for R ¹ has 1 carbon atom
To 10 unsaturated aliphatic hydrocarbon groups, saturated aliphatic hydrocarbon groups, or aromatic hydrocarbon groups. Particularly preferably, it is an unsaturated aliphatic hydrocarbon group having 1 to 8 carbon atoms, a saturated aliphatic hydrocarbon group, or an aromatic hydrocarbon group. Specific examples include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, n-pentyl, n-amyl,
Examples thereof include n-hexyl, isoamyl, cyclopentyl, cyclohexyl, phenyl and octyl groups.

A preferred hydrocarbon group for R ² has 1 carbon atom
~ 10 unsaturated or saturated aliphatic hydrocarbon groups. An unsaturated or saturated aliphatic hydrocarbon group having 1 to 8 carbon atoms is particularly preferable. Specific examples include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, n-pentyl, n-amyl, n-hexyl, isoamyl,
Examples include cyclopentyl, cyclohexyl, phenyl and octyl groups. However, when R ¹ is an aromatic hydrocarbon group such as a phenyl group, an organic silicon compound in which R ² is an ethyl group, that is, phenyldiethylaminodiethoxysilane is not preferable. When R ¹ is an aromatic hydrocarbon group such as a phenyl group, an organic silicon compound in which R ² is a methyl group, that is, phenyldiethylaminodimethoxysilane is particularly preferably used.

Preferred hydrocarbon groups as R ³ and R ⁴ are unsaturated or saturated aliphatic hydrocarbon groups having 1 to 10 carbon atoms. An unsaturated or saturated aliphatic hydrocarbon group having 1 to 8 carbon atoms is particularly preferable. Specific examples include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, n-pentyl, n-amyl, n-hexyl, isoamyl, cyclopentyl, cyclohexyl, phenyl and octyl groups.

R ¹ Si (OR ² ) in which n is 1 in the general formula (I)
A dialkoxysilane compound represented by ₂ (NR ³ R ⁴ ) or a trialkoxysilane compound represented by Si (OR ² ) ₃ (NR ³ R ⁴ ) in which n is 0 is preferably used.

Preferred compounds of component [C] include R ³
And a compound containing a diethylamino group in which R ⁴ is an ethyl group, more preferably a dimethoxylane compound containing a diethylamino group in which R ² is a methyl group.

Further, in the relation of R ¹ , R ³ and R ⁴ ,
When R ¹ is a hydrocarbon group having a small number of carbon atoms and no branching, an organosilicon compound in which at least one of R ³ and R ⁴ is a branched hydrocarbon group is preferably used. Hydrocarbon group-containing aminodimethoxysilanes having a branch, phenyl group-containing aminodimethoxysilanes, branched hydrocarbon group-containing aminotrimethoxysilanes, phenyl group-containing aminotrimethoxysilanes, branched hydrocarbon groups and phenyl Examples thereof include group-containing aminodimethoxysilanes.

Specific examples of the diethylamino group-containing dimethoxylane compounds include methyl (diethylamino) dimethoxysilane, ethyl (diethylamino) dimethoxysilane, isopropyl (diethylamino) dimethoxysilane, n-propyl (diethylamino) dimethoxysilane, vinyl. Examples thereof include (diethylamino) dimethoxysilane, phenyl (diethylamino) dimethoxysilane, cyclohexyl (diethylamino) dimethoxysilane.

Specific compounds of branched hydrocarbon group-containing aminodimethoxyxylans include methyl (isopropylmethylamino) dimethoxysilane, methyl (isopropylethylamino) dimethoxysilane, methyl (diisopropylamino) dimethoxysilane, ethyl ( Isopropylmethylamino) dimethoxysilane, ethyl (isopropylethylamino) dimethoxysilane, ethyl (diisopropylamino) dimethoxysilane, propyl (isopropylmethylamino) dimethoxysilane,
Isopropylaminosilane such as propyl (isopropylethylamino) dimethoxysilane, propyl (diisopropylamino) dimethoxysilane, methyl (isobutylmethylamino) dimethoxysilane, methyl (isobutylethylamino) dimethoxysilane, methyl (diisobutylamino) dimethoxysilane, ethyl (isobutyl) Methylamino) dimethoxysilane, ethyl (isobutylethylamino) dimethoxysilane, ethyl (diisobutylamino) dimethoxysilane, propyl (isobutylmethylamino) dimethoxysilane, propyl (isobutylethylamino) dimethoxysilane, propyl (diisobutylamino) dimethoxysilane, etc. Isobutylaminosilane, methyl (t-butylmethylamino) dimethoxysilane, methyl (t-butyl Ruethylamino) dimethoxysilane, methyl (di-t-butylamino) dimethoxysilane, ethyl (t-butylmethylamino) dimethoxysilane, ethyl (t-butylethylamino) dimethoxysilane, ethyl (di-t-butylamino) dimethoxysilane, propyl (T-
Butylmethylamino) dimethoxysilane, propyl (t-
Butylethylamino) dimethoxysilane, propyl (diethyl
Examples thereof include t-butylaminosilane such as t-butylamino) dimethoxysilane.

Specific examples of the phenyl group-containing aminodimethoxyxylans include methyl (phenylmethylamino) dimethoxysilane, methyl (phenylethylamino) dimethoxysilane, methyl (phenylpropylamino) dimethoxysilane and propyl (phenylmethylamino). ) Dimethoxysilane, propyl (phenylethylamino) dimethoxysilane, propyl (phenylpropylamino) dimethoxysilane, propyl (phenylbutylamino) dimethoxysilane, ethyl (diphenylamino) dimethoxysilane, methyl (phenylbutylamino) dimethoxysilane, methyl ( Phenylmethylamino) dimethoxysilane, ethyl (phenylethylamino) dimethoxysilane, ethyl (phenylpropylamino) dimethoxysilane, Pill (diphenylamino)
Examples include dimethoxysilane.

Specific examples of the branched hydrocarbon group- and phenyl group-containing aminodimethoxyxylans include methyl (phenylisopropylamino) dimethoxysilane, methyl (phenylisobutylamino) dimethoxysilane, and methyl (phenyl t-butylamino). ) Dimethoxysilane, ethyl (phenylisopropylamino) dimethoxysilane, ethyl (phenylbutylamino) dimethoxysilane, ethyl (phenylisobutylamino) dimethoxysilane, ethyl (phenyl t-butylamino) dimethoxysilane, propyl (phenylisopropylamino) dimethoxysilane , Propyl (phenylisobutylamino) dimethoxysilane, propyl (phenyl t-butylamino) dimethoxysilane and the like.

In addition to the above-mentioned dimethoxysilane compounds, trimethoxysilanes such as (isopropylmethylamino) trimethoxysilane, (isopropylethylamino) trimethoxysilane, (isobutylmethylamino) trimethoxysilane and (isobutylethylamino). )
Trimethoxysilane, (t-butylmethylamino) trimethoxysilane, (t-butylethylamino) trimethoxysilane, (phenylmethylamino) trimethoxysilane, (phenylethylamino) trimethoxysilane,
(Phenylpropylamino) trimethoxysilane, (phenylisopropylamino) trimethoxysilane, (phenylbutylamino) trimethoxysilane, (phenylisobutylamino) trimethoxysilane, (phenyl t-
(Butylamino) trimethoxysilane, (diisopropylamino) trimethoxysilane, (diisobutylamino)
Examples thereof include trimethoxysilane and (di-t-butylamino) trimethoxysilane.

Further, aminosilanes in which R ^{1 of} the above formula (I) is a branched hydrocarbon group, for example, isopropyl (dimethylamino) dimethoxysilane, isopropyl (methylethylamino) dimethoxysilane, isopropyl (methylpropylamino) ) Dimethoxysilane, isopropyl (diethylamino) dimethoxysilane, isopropyl (dipropylamino) dimethoxysilane, isopropyl (propylethylamino) dimethoxysilane, isobutyl (dimethylamino) dimethoxysilane, isobutyl (methylethylamino) dimethoxysilane, isobutyl (diethylamino) Dimethoxysilane, isobutyl (dipropylamino) dimethoxysilane, t-butyl (dimethylamino) dimethoxysilane, t-butyl (methylethylamino) dimethoxy Silane, t-butyl (diethylamino) dimethoxysilane, cyclopentyl (dimethylamino) dimethoxysilane, cyclopentyl (methylethylamino) dimethoxysilane, cyclopentyl (diethylamino) dimethoxysilane, cyclopentyl (dipropylamino) dimethoxysilane, cyclohexyl (dimethylamino) dimethoxy Examples thereof include silane, cyclohexyl (methylethylamino) dimethoxysilane, cyclohexyl (diethylamino) dimethoxysilane, and cyclohexyl (dipropylamino) dimethoxysilane.

Examples of the dialkyl (dialkylamino) alkoxysilane compound in which n in the general formula (I) is 2 include diisopropyl (diethylamino) methoxysilane.

Of the above organosilicon compounds, the following compounds can be preferably used. Methyldiethylaminodimethoxysilane, ethyldiethylaminodimethoxysilane, n-propyldiethylaminodimethoxysilane, isopropyldiethylaminodimethoxysilane, n-
Butyldiethylaminodimethoxysilane, isobutyldiethylaminodimethoxysilane, ter-butyldiethylaminodimethoxysilane, vinyldiethylaminodimethoxysilane, cyclohexyldiethylaminodimethoxysilane, cyclopentyldiethylaminodimethoxysilane, methyldi-n-propylaminodimethoxysilane and the like are preferably used.

Further, methyldiisopropylaminodimethoxysilane, ethyldiisopropylaminodimethoxysilane and the like are preferably used.

Further, phenyldiethylaminodimethoxysilane is preferably used.

The above-mentioned organosilicon compound can be prepared, for example, by reacting a tetraalkoxysilane with a Griyal compound.

The amount of the component [C] used is the element ratio of the silane of the component [C] to the aluminum of the component [B] (Si / Al).
0.01 to 1 is preferable, and 0.05 to 0.33 is particularly preferable.

In the present invention, a chain transfer agent such as hydrogen can be used. The amount of hydrogen used for producing an α-olefin polymer having desired stereoregularity (HI) and melt fluidity (MFR) can be appropriately determined depending on the polymerization method and the polymerization conditions, but usually, Hydrogen partial pressure
It is in the range of 0.05 to 1.0.

In the present invention, during the α-olefin polymerization,
The order of contact of the catalyst components is not particularly limited, but it is not preferable that only the organosilicon compound of the component [C] and the catalyst solid of the component [A] come into direct contact with each other.

Examples of the α-olefin used in the present invention include propylene, 1-butene, 1-hexene, 4-methylpentene-1 and 1-octene. In the present invention, the above α-olefin can be homopolymerized or copolymerized, and further the above α-olefin and ethylene can be copolymerized. In the present invention, propylene can be homopolymerized, and then ethylene or a mixture of ethylene and propylene can be copolymerized in the presence of the homopolymer to produce a propylene block copolymer.

As the polymerization method in the present invention, a slurry polymerization method using a non-polar solvent such as hexane or heptane, a gas phase polymerization method in which a monomer is brought into contact with a catalyst in a gas state, or a monomer in a liquid state as a solvent is used. A bulk polymerization method or the like in which the polymerization is performed can be adopted. Polymerization pressure is 1
~ 200kg / cm ² , preferably 10 ~ 80kg / cm ² , the polymerization temperature is usually 10 ~ 100 ℃, preferably 30 ~ 90 ℃, the polymerization time is usually
It is in the range of 0.1 to 10 hours, preferably 0.5 to 7 hours.

Further, in the present invention, it is preferable to carry out the main polymerization after prepolymerizing the olefin according to the above-mentioned various polymerization methods. In the pre-polymerization, the catalyst solid component [A] is contact-treated with the organoaluminum compound component [B] and the organosilicon compound component [C] in advance before the main polymerization,
Contact-treated solids can be prepared by washing the solids. Further, using the catalyst solid component [A] or the above-mentioned catalytically treated solid, in the presence of the organoaluminum compound component [B] and the organosilicon compound component [C], a limited amount of α
It is also possible to prepolymerize the olefins. When the contact-treated solid is used, the organosilicon compound component [C] can be omitted in the prepolymerization. By using these contact-treated solids, prepolymerized solids, or washed solids after prepolymerization in the main polymerization, the polymerization activity per catalyst solid and the stereoregularity of the polymer can be improved.

In the present invention, when the above-mentioned contact-treated solid or prepolymerized solid is used as the catalyst solid component in the main polymerization, the organosilicon compound component [C] can be omitted in the main polymerization.

As the contact treatment of the present invention, the component [A],
The component [B] and the component [C] are mixed and usually 0 to 100
React at 0.1 ℃ for 10 to 10 hours. The order of mixing each component is not particularly limited, but in general, the order of the component [A], the component [B], and the component [C] is preferable. After the contact treatment, the solid is washed with an inert hydrocarbon solvent, filtered and separated to be used as a catalyst solid component in prepolymerization or main polymerization.

The prepolymerization in the present invention can be carried out by a gas phase method, a slurry method, a bulk method or the like. The solid obtained in the prepolymerization can be separated and then used in the main polymerization, or the main polymerization can be continuously carried out without separation.

The prepolymerization time is usually 0.1 to 10 hours,
It is preferable to continue the prepolymerization until 0.1 to 100 g of the prepolymer is produced per 1 g of the catalyst solid component. Catalyst solid component
If it is less than 0.1 g per 1 g, the main polymerization activity will be insufficient and the amount of catalyst residue will increase, and the stereoregularity of the α-olefin polymer will be insufficient. If it exceeds 100 g, the crystallinity of the α-olefin polymer tends to decrease. The prepolymerization temperature is
It is carried out at 0 to 100 ° C, preferably 10 to 90 ° C in the presence of each catalyst component. When carrying out the prepolymerization at a high temperature exceeding 50 ° C., it is preferable to reduce the α-olefin concentration or shorten the polymerization time. Otherwise catalyst solid component
It is difficult to control the production of 0.1 to 100 g of the prepolymer per 1 g, and the crystallinity of the α-olefin polymer obtained by the main polymerization is lowered.

The amount of the organoaluminum component used in the prepolymerization is usually Al / Ti with respect to the titanium atom of the catalyst solid component.
The molar ratio is 0.5 to 1000, preferably 1 to 100. The amount of the silicate compound to be used is usually such that the Si / Al molar ratio to the aluminum atom of the organoaluminum compound component is 0.01 to
1, preferably 0.1 to 0.5. Further, hydrogen can be allowed to coexist in the preliminary polymerization, if necessary.

[0044]

When an α-olefin is produced using the catalyst of the present invention, an α-olefin polymer having high activity, high stereoregularity of the polymer and high melt flowability can be provided.

EXAMPLES Examples of the present invention will be described below. In the examples, “polymerization activity” means a catalyst solid component.
Yield (g) of polymer produced per gram. The stereoregularity (HI) of a polymer indicates the ratio (%) of the balance of the polymer extracted with hot heptane for 20 hours.

The melt flowability (MFR) of the polymer is ASTM D-12
It represents the weight (g) of the molten polymer for 10 minutes under the load of 2.16 kg measured at 230 ° C. according to 38.

The molecular weight distribution was determined by GPC using polystyrene as a standard substance (150CV type manufactured by Waters Co., o-dichlorobenzene solvent, column SHODEX, temperature 145 ° C., concentration).
Was evaluated by the ratio M _w / M _n of weight average molecular weight M _w and number-average molecular weight M _n determined from 0.05 wt%).

The melting point (Tm), crystallization temperature (Tc) and heat of fusion of crystal (ΔH) are DSC (Seiko Denshi Kogyo ASC-520).
0). Room temperature to 230 ℃
Up to 10 ° C / min and hold for 5 minutes,
The crystallization temperature was determined by lowering the temperature from 230 ℃ to 40 ℃ at a rate of 5 ℃ / min. Furthermore, the melting point and heat of fusion of crystals are from 40 ° C
It was determined by heating up to 230 ° C at a rate of 10 ° C / min.

Isopentad fraction (mmmm)% is Macrom
¹³ C-N attributed based on olelcules 8 , 687 (1975)
It was calculated from the MR spectrum. ^{The 13} C-NMR spectrum was measured using a JEOL EX-400 device, TMS as a reference, and a temperature of 130 ° C. in an o-dichlorobenzene solvent.

Reference Example Synthesis Example of Organosilicon Compound (Isopropyldiethylaminodimethoxysilane) A stirrer piece was placed in a glass filter-equipped flask (capacity 400 mL) equipped with a dropping funnel, and the inside of the flask was replaced with nitrogen by using a vacuum pump. , Tetramethoxysilane 17.7mL (0.12mol) and isopropyl ether 60mL
I put it in. 60 mL of a 2 mol / L isopropylmagnesium bromide diethyl ether solution was placed in the dropping funnel, and the mixture was slowly added dropwise to the flask under ice cooling, followed by stirring at room temperature for 12 hours. After confirming that the desired product was sufficiently produced, the precipitate was filtered with a glass filter. Isopropyl ether in the filtrate was distilled off, and the product was subjected to primary distillation and secondary distillation to obtain isopropyltrimethoxysilane.

Next, a stirrer piece was placed in a glass filter-equipped flask (capacity 400 mL) equipped with a dropping funnel, and the inside of the flask was replaced with nitrogen using a vacuum pump, followed by distillation with diethylamine 5.2 mL (0.05 mol). 25 mL of dehydrated n-heptane was added. For the dropping funnel, 30.1 mL of 1.66 mol / L butyl lithium hexane solution or 25 mL of 2 mol / L ethylmagnesium chloride diethyl ether solution
Then, 8.78 g (0.05 mol) of isopropyltrimethoxysilane synthesized above was slowly added dropwise to the flask under ice cooling, and then the mixture was stirred at room temperature for 12 hours. After confirming that the desired product was sufficiently produced, the precipitate was filtered with a glass filter. The n-heptane in the filtrate was distilled off, and the product was subjected to primary distillation and secondary distillation to obtain the target product, isopropyldiethylaminodimethoxysilane. The boiling point of this compound was 61.5 ° C / 12 mmHg.

Examples 1 to 3 (1) Preparation of solid catalyst component [A] 15 mmol of anhydrous aluminum chloride was added to 40 ml of toluene, and then 15 mmol of methyltriethoxysilane was added dropwise with stirring. The reaction was carried out at ℃ for 1 hour. After cooling the reaction product to -5 ° C, 18 ml of diisopropyl ether containing 30 mmol of butylmagnesium chloride was added dropwise to the reaction product over 30 minutes with stirring, and the temperature of the reaction solution was adjusted to within the range of -5 to 0 ° C. I kept it. After the dropping was completed, the temperature was gradually raised and the reaction was continued at 30 ° C. for 1 hour. The precipitated solid was filtered off and washed with toluene and n-heptane. Next, 4.9 g of the obtained solid was suspended in 30 ml of toluene, and 150 mmol of titanium tetrachloride and 3.3 mmol of di-n-heptyl phthalate were suspended in this suspension.
Mmol was added, and the mixture was reacted at 90 ° C. for 1 hour with stirring.
The solid was filtered off at the same temperature and washed with toluene and then n-heptane. Furthermore, the solid was suspended again in 30 ml of toluene, 150 mmol of titanium tetrachloride was added, and the mixture was stirred at 90 ° C.
And reacted for 1 hour. The solid was filtered off at the same temperature, and the solid was washed with toluene and then n-heptane. The titanium content in the obtained catalyst solid component was 3.55% by weight. This solid was suspended in 80 ml of heptane to prepare a heptane slurry of catalyst solid components.

(2) Polymerization of Propylene A glass ampoule containing a heptane slurry of catalyst solids (7.9 mg as catalyst solids) was attached to an autoclave with an internal volume of 2 L equipped with a stirrer, and then the inside of the autoclave was replaced with nitrogen. . Then triethyl aluminum
2.1 ml of n-heptane solution containing 2.1 mmol was charged to the autoclave. Furthermore, n-heptane solution containing 0.35 mmol of the silane compound shown in Table 1 as the third component 1.
74 ml was charged. Then, after introducing 1.0 kg / cm ² G of hydrogen, 1200 ml of liquid propylene was introduced and the autoclave was shaken. Cool the autoclave to 10 ° C, crush the glass ampoule containing the solid catalyst components with stirring, and
Prepolymerized for minutes. Subsequently, the temperature inside the autoclave was raised to 70 ° C, and polymerization was carried out at 70 ° C for 1 hour. After completion of the polymerization, unreacted propylene gas was released, and the polymer was dried under reduced pressure at 50 ° C. for 20 hours to obtain white powdery polypropylene. Tables 6 and 11 show the measurement results of the polymerization activity and the characteristics of the polymer.

Examples 4 to 7 Polymerization of propylene was carried out in the same manner as in Example 1 except that the silane compounds shown in Table 2 were used as the third component and the hydrogen pressure shown in Table 7 was used. The results are shown in Tables 7 and 12.

Examples 8 to 11 Propylene was polymerized in the same manner as in Example 1 except that the silane compounds shown in Table 3 were used as the third component. The results are shown in Tables 8 and 13.

Examples 12 to 17 Propylene was polymerized in the same manner as in Example 1 except that the silane compounds shown in Table 4 were used as the third component and the hydrogen pressure shown in Table 9 was used. The results are shown in Table 9 and Table 14.

Comparative Example 1 Propylene was polymerized in the same manner as in Example 1 except that phenyl (diethylamino) diethoxysilane was used as the third component. The results are shown in Tables 10 and 15.

Examples 18 to 19 Polymerization of propylene was carried out in the same manner as in Example 1 except that the silane compounds shown in Table 16 were used as the third component and the hydrogen pressure was 1.0 kg / cm ² . . The results are shown in Table 1.
7 shows.

[0059]

[Table 1]

[0060]

[Table 2]

[0061]

[Table 3]

[0062]

[Table 4]

[0063]

[Table 5]

[0064]

[Table 6]

[0065]

[Table 7]

[0066]

[Table 8]

[0067]

[Table 9]

[0068]

[Table 10]

[0069]

[Table 11]

[0070]

[Table 12]

[0071]

[Table 13]

[0072]

[Table 14]

[0073]

[Table 15]

[0074]

[Table 16]

[0075]

[Table 17]

[0076]

[Brief description of drawings]

FIG. 1 is a flow chart showing a preparation process and a polymerization method of a catalyst component of the present invention.

 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Jun Yamashita 8-1 Goi Minamikaigan, Ichihara-shi, Chiba Ube Industries Ltd. Chiba Research Institute (72) Inventor Katsunori Sato 8th Goi Minamikaigan, Ichihara-shi, Chiba 1 Ube Industries, Ltd. Chiba Laboratory

Claims (1)

[Claims] 1. A catalyst solid component essentially comprising magnesium, titanium, a halogen element, and an electron donor as the component [A], an organoaluminum compound component as the component [B], and a general formula (I) as the component [C]. R ¹ _n Si (OR ² ) _3-n (NR ³ R ⁴ ) (I) (In the formula, R ¹ represents an aliphatic hydrocarbon group or aromatic hydrocarbon group having 1 to 24 carbon atoms, and R ² represents A hydrocarbon group having 1 to 24 carbon atoms (however, when R ¹ is an aromatic hydrocarbon group, R ² excludes an ethyl group), R ³ and R ⁴ are hydrocarbon groups having 1 to 24 carbon atoms And n is 0 to 2) in the presence of a catalyst consisting of an organosilicon compound represented by the formula: α-olefin.