JP2568205B2 - Method for drying solid catalyst component for olefin polymerization - Google Patents

Description

TECHNICAL FIELD The present invention relates to a method for drying a solid catalyst component for olefin polymerization. More specifically, the present invention relates to a method for drying a solid catalyst component which is highly active when applied to the polymerization of olefins and which enables the production of a polymer having good polymer properties.

BACKGROUND OF THE INVENTION Conventionally, when the solid catalyst component for olefin polymerization is handled, that is, stored or stored, and transported, there are roughly two methods for storing the solid catalyst component. One is a method of making a slurry in an inert solvent such as liquid hydrocarbon, and the other is
This is a method in which the material is dried and is substantially free of solvent.

The former method often leaves problems in storage and transportation of the solid catalyst component, and improvement is desired. On the other hand, the latter method can solve the problem of the former,
Also, new problems usually occur. That is, when the solid catalyst component is dried, agglomeration is likely to occur and a coarse particle solid catalyst component is produced.

The formation of these coarse particles causes various problems such as deterioration of catalyst activity, deterioration of polymer properties, and blockage of catalyst and polymer polymer in a line or at a valve. Therefore, it is desired to develop a drying method that does not cause the above various problems.

Prior Art As prior art, JP-A-55-135105 and JP-A-56-136805
No. 62-50308 and the like. In these prior arts, by leaving a small amount of liquid hydrocarbon or high-boiling-point liquid hydrocarbon in the solid catalyst component, it is said that a solid catalyst component having high performance can be obtained without problems such as storage stability. However, these methods do not seem to give a sufficient solution to the above-mentioned problem of coarse particles generated during drying, and a new technique is required.

SUMMARY OF THE INVENTION The present invention provides a solid catalyst component for olefin polymerization containing tetravalent titanium, magnesium and halogen as essential components, a silicon compound of the following formula, (However, R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ each independently represent hydrogen or a hydrocarbon residue, and n is such that the viscosity of this silicon compound is about 1 to 1000 centistokes. The present invention provides a method for drying a solid catalyst component for olefin polymerization, which comprises contacting with or dispersing in a liquid hydrocarbon containing the above number) and then drying.

EFFECTS OF THE INVENTION According to the method for drying a solid catalyst component for olefin polymerization of the present invention, it is possible to prevent the formation of coarse particles due to aggregation of the solid catalyst component, which easily occurs during drying. As a result, the following effects are recognized.

(B) There is no deterioration in catalyst performance due to drying. For example, there is no deterioration in performance such as catalytic activity, polymer properties, and stereoregularity in the polymerization of propylene.

(B) Operation stability is good during polymer polymerization. Coarse particles of the solid catalyst component generally produce a coarse polymer, which causes troubles such as adhesion of the polymer in the polymerization tank where the line and the valve are closed. The drying method of the present invention can solve all of these problems. Of course, it goes without saying that the same troubles as described above attributable to the coarse particles themselves of the catalyst can be solved.

Detailed Description of the Invention (Solid catalyst component) The solid catalyst component for olefin polymerization used in the present invention is a solid component containing titanium, magnesium and halogen as essential components. Here, "containing as an essential component" means that other than the three listed components may contain a purposeful other element, and each of these elements exists as a purposeful arbitrary compound. And that these elements may exist as bonded to each other.

Such solid components are known. For example, JP-A-53-45688, JP-A-54-3894, JP-A-54-31092 and JP-A-54-39.
483, 54-94591, 54-118484, 54-131589
No. 55, No. 55-75411, No. 55-90510, No. 55-90511, No. 55
-127405, 55-147507, 55-155003, 56-1860
No. 9, No. 56-70005, No. 56-72001, No. 56-86905, No. 5
6-90807, 56-155206, 57-3803, 57-34103
No. 57, No. 57-92007, No. 57-121003, No. 58-5309, No. 58
-5310, 58-5311, 58-8706, 58-27732,
58-32604, 58-32605, 58-67703, 58-117
No. 206, No. 58-127708, No. 58-183708, No. 58-183709
No. 59-149905, No. 59-149906, etc. are used.

Examples of the magnesium compound serving as the magnesium source of the solid catalyst component used in the present invention include magnesium halide, dialkoxy magnesium, alkoxy magnesium halide, magnesium oxyhalide, dialkyl magnesium, magnesium oxide, magnesium hydroxide, and carboxylates of magnesium. Can be given.

The titanium compound serving as the titanium source is a tetravalent titanium compound, and has a general formula of Ti (OR ⁴ ) _4-n X _n (wherein R ⁴ is a hydrocarbon residue, preferably having about 1 to 10 carbon atoms). X is halogen, and n is a number of 0 ≦ n ≦ 4.). Specific examples include TiCl ₄ , TiBr ₄ , Ti (OC ₂ H ₅ ) Cl ₃ , Ti (OC ₂ H ₅ ) ₂ Cl ₂ , Ti
(OC ₂ H ₅ ) ₃ Cl, Ti (O-iC ₃ H ₇ ) Cl ₃ , Ti (O-nC ₄ H ₉ ) Cl ₃ , Ti (On
C ₄ H ₉ ) ₂ Cl ₂ , Ti (OC ₂ H ₅ ) Br ₃ , Ti (OC ₂ H ₅ ) (OC ₄ H ₉ ) ₂ Cl, Ti (O
-nC ₄ H ₉ ) ₃ Cl, Ti (OC ₆ H ₅ ) Cl ₃ , Ti (O-iC ₄ H ₉ ) ₂ Cl ₂ , Ti (OC ₅
H ₁₁ ) Cl ₃ , Ti (OC ₆ H ₁₃ ) Cl ₃ , Ti (OC ₂ H ₅ ) ₄ , Ti (O-nC ₃ H ₇ ) ₄ ,
Ti (O-nC ₄ H ₉ ) ₄ , Ti (O-iC ₄ H ₉ ) ₄ , Ti (O-nC ₆ H ₁₃ ) ₄ , Ti (O-nC
₈ H _{17) 4,} Ti _{[OCH 2 CH (C 2 H 5} ) C 4 H 9 ] is _4, and the like.

Further, it is also possible to use a molecular compound obtained by reacting TiX ' ₄ (here, X'represents halogen) with an electron donor described later. Specific examples include TiCl ₄ .CH ₃ COC ₂ H ₅ , TiCl ₄ .C
_{H 3 CO 2 C 2 H 5} , TiCl 4 · C 6 H 5 NO 2, TiCl 4 · CH 3 COCl, TiCl 4 · C 6 H
₅ COCl, TiCl ₄ / C ₆ H ₅ CO ₂ H ₅ , TiCl ₄ / ClCOC ₂ H ₅ , TiCl ₄ / C ₄ H ₄
O etc.

The halogen source is usually supplied from the above-mentioned halogen compound of magnesium and / or titanium, but is supplied from a known halogenating agent such as a halide of aluminum, a halide of silicon, and a halide of phosphorus. You can also.

The halogen contained in the catalyst component may be fluorine, chlorine, bromine, iodine or a mixture thereof, with chlorine being particularly preferred.

Solid components used in the present invention include SiCl in addition to the above essential components.
₄ , CH ₃ SiCl ₃ , silicon compounds such as methylhydrogenpolysiloxane, Al (O-iC ₃ H ₇ ) ₃ , AlCl ₃ , AlBr ₃ , Al (OC _{2
H 5) 3, Al (OCH} 3) 2 aluminum compounds such as Cl and B (OCH ₃₎
Other components such as boron compounds such as ₃ , B (OC ₂ H ₅ ) ₃ and B (OC ₆ H ₅ ) ₃ can also be used, and these remain in the solid component as components such as silicon, aluminum and boron. It doesn't matter what you do.

Furthermore, when producing this solid component, it can also be produced using an electron donor as an internal donor.

Examples of electron donors (internal donors) that can be used in the production of this solid component include alcohols, phenols, ketones, aldehydes, carboxylic acids, esters of organic acids or inorganic acids, ethers, acid amides, acids. Examples thereof include oxygen-containing electron donors such as anhydrides, nitrogen-containing electron donors such as ammonia, amines, nitriles and isocyanates.

More specifically, (a) a compound having 1 carbon atom such as methanol, ethanol, propanol, pentanol, hexanol, octanol, dodecanol, octadecyl alcohol, benzyl alcohol, phenylethyl alcohol, cumyl alcohol, and isopropylbenzyl alcohol;
To 18 alcohols, (b) phenols, cresols, xylenols, ethylphenols, propylphenols, cumylphenols, nonylphenols, naphthols, and other alkyl groups having 6 to 25 carbon atoms, (c) Acetone, methyl ethyl ketone, methyl isobutyl ketone, acetophenone, benzophenone and other C3 to C15 ketones, (d) acetaldehyde, propionaldehyde, octyl aldehyde, benzaldehyde, tolualdehyde, naphthaldehyde and other C2 to C15 aldehydes , (V) methyl formate, methyl acetate, ethyl acetate, vinyl acetate, propyl acetate, octyl acetate, cyclohexyl acetate, ethyl propionate, methyl butyrate, ethyl valerate, ethyl stearate, chloroacetic acid Chill, dichloroacetic ethyl acetate, methyl methacrylate, ethyl crotonate, cyclohexanecarboxylate, methyl benzoate, ethyl benzoate,
Propyl benzoate, butyl benzoate, octyl benzoate, cyclohexyl benzoate, phenyl benzoate, benzyl benzoate, methyl toluate, ethyl toluate,
Amyl toluate, ethyl ethyl benzoate, methyl anisate, ethyl anisate, ethyl ethoxy benzoate, diethyl phthalate, dibutyl phthalate, diheptyl phthalate, γ-butyrolactone, α-valerolactone, coumarin, phthalide, ethylene carbonate, etc. Organic acid esters having 2 to 20 carbon atoms; (f) inorganic acid esters such as silicates such as ethyl silicate, butyl silicate, and phenyltriethoxysilane; (g) acetyl chloride;
Benzoyl chloride, toluic acid chloride, anisic acid chloride, phthaloyl chloride, isochlorophthaloyl and other acid halides having 2 to 15 carbon atoms, (thi) methyl ether, ethyl ether, isopropyl ether, butyl ether, amyl ether, tetrahydrofuran, anisole, C2-C20 ethers such as diphenyl ether, acid amides such as (li) acetic acid amide, benzoic acid amide, toluic acid amide, (nu) methylamine, ethylamine, diethylamine, tributylamine, piperidine, tribenz Examples thereof include amines such as ruamine, aniline, pyridine, picoline, and tetramethylethylenediamine, nitriles such as (l) acetonitrile, benzonitrile, and tolunitrile. Two or more of these electron donors can be used.

The amount of each component used may be arbitrary as long as the effects of the present invention are recognized, but generally, the following ranges are preferable.

The titanium compound may be used in a molar ratio of 1 × 10 ^{−4 to} 1000, preferably 0.01 to 10 with respect to the amount of the magnesium compound used. When a compound for that purpose is used as a halogen source, the molar amount of the compound is 1 × 10 ⁻ with respect to the amount of magnesium used, regardless of whether the titanium compound and / or the magnesium compound contains halogen. ^It is preferably in the range of ^{2 to} 1000, and more preferably in the range of 0.1 to 100. The amount of silicon, aluminum, and boron compounds used is 1 × 10 6 in molar ratio with respect to the amount of magnesium compound used above.
^It is preferably in the range of ^{-3 to} 100, and more preferably in the range of 0.01 to 1.

The amount of the electron-donating compound used is preferably in the range of 1 × 10 ⁻³ to 10 with respect to the amount of the above-mentioned magnesium compound used, and more preferably in the range of 0.01 to 5.

The above-mentioned solid catalyst component is produced, for example, by the following production method using the above-mentioned titanium source, magnesium source and halogen source, and optionally other components such as an electron donor.

(A) A method in which a magnesium halide is optionally contacted with an electron donor and a titanium-containing compound.

(B) A method of treating alumina or magnesium with a phosphorus halide compound, and bringing it into contact with a magnesium halide, an electron donor, and a titanium halogen-containing compound.

(C) A method of contacting a titanium halide and / or a silicon halide with a solid component obtained by contacting a magnesium halide with a titanium tetraalkoxide and a specific polymer silicon compound.

As the polymer silicon compound, those represented by the following formula are suitable.

(Here, R is a hydrocarbon residue having about 1 to 10 carbon atoms, and n is the degree of polymerization such that the viscosity of the polymer silicon compound is about 1 to 100 centistokes.) Of these, methylhydrogen Ene polysiloxane, ethylhydrogen polysiloxane, 1,3,5,7
Tetramethylcyclotetrasiloxane, 1,3,5,7,9 pentamethylcyclopentasiloxane, phenylhydrogenpolysiloxane and cyclohexylhydrogenpolysiloxane are particularly preferred.

(D) A method in which a magnesium compound is dissolved with titanium tetraalkoxide and an electron donor, and a titanium compound is brought into contact with a solid component precipitated with a halogenating agent or a titanium halogen compound.

(E) A method in which an organomagnesium compound such as a Grignard reagent is allowed to act with a halogenating agent, a reducing agent, and the like, and then contacted with an electron donor and a titanium compound as necessary.

(F) A method of bringing a halogenating agent and / or a titanium compound into contact with an alkoxymagnesium compound in the presence or absence of an electron donor.

As the catalyst component for olefin polymerization used in the present invention, the solid component obtained as described above can be used as it is, or the solid component obtained by contacting the solid component with olefins in the presence of an organoaluminum compound is preliminarily polymerized. Can also be used as

When prepolymerized, the prepolymerization conditions are not particularly limited, but the following conditions are generally preferred.
The polymerization temperature is 0 to 80 ° C, preferably 10 to 60 ° C. The amount of polymerization is 1 gram of the above solid contact component
It is preferred to polymerize 0.001 to 50 grams of olefins, more preferably 0.1 to 10 grams of olefins.

As the organoaluminum component at the time of prepolymerization, those generally known can be used.

As a specific example, Al (C ₂ H ₅ ) ₃ , Al (isoC ₄ H ₉ ) ₃ , Al (C ₅ H
_{13) 3, Al (C 8} H 17) 3, Al (C 10 H 17) 3, Al (C 10 H 21) 3, Al (C 2 H
₅ ) ₂ Cl, Al (isoC ₄ H ₉ ) ₂ Cl, Al (C ₂ H ₅ ) ₂ H, Al (isoC ₄ H ₉ ) ₂ H,
Examples thereof include Al (C ₂ H ₅ ) ₂ (OC ₂ H ₅ ).

Of these, Al (C ₂ H ₅ ) ₃ and Al (isoC ₄ H ₉ ) ₃ are preferable.
Is. It is also effective to use a combination of a trialkylaluminum and an alkylaluminum halide, or a combination of a trialkylaluminum, an alkylaluminum halide and an alkylaluminum ethoxide.

As a specific example, the combination of Al (C ₂ H ₅ ) ₃ and Al (C ₂ H ₅ ) ₂ Cl
Combined use of (isoC ₄ H ₉ ) ₃ and Al (isoC ₄ H ₉ ) ₂ Cl, Al (C ₂ H ₅ ) ₃ and Al (C ₂
H ₅ ) _1.5 Cl _1.5 combined use, Al (C ₂ H ₅ ) ₃ and Al (C ₂ H ₅ ) ₂ Cl and Al (C
₂ H ₅ ) ₂ (OC ₂ H ₅ ) may be used in combination.

The amount of the organoaluminum component used during the prepolymerization is 1 to 20, preferably 2 to 10 in terms of Al / Ti (molar ratio) with respect to the Ti component in the molded solid catalyst component. In addition to these, known electron donors such as alcohols, esters and ketones can be added during the prepolymerization.

Examples of the olefin used in the prepolymerization include ethylene, propylene, 1-butene, 1-hexene, 4-methyl-pentene-1 and the like. It is also possible to make hydrogen coexist during the prepolymerization.

Thus, a solid catalyst component for olefin polymerization containing titanium, magnesium and halogen as essential components is obtained.

In the method of the present invention, titanium, magnesium and halogen obtained as described above, during the production of a solid catalyst component for olefin polymerization containing as essential components, the general formula R ⁷ mXnSi (OR ⁸ ) _4-mn (however , R ⁷ and R ⁸ are hydrocarbon residues, X is halogen, m and n
Are 0 ≦ m ≦ 3 and 0 ≦ n ≦ 3, respectively, and 0 ≦ m + n ≦ 3), and are preferably used in contact with the compound. Here, it is preferable that R ⁷ and R ⁸ are each a hydrocarbon residue of about 1 to 20, preferably 1 to 10. X is preferably chlorine, at least for economic reasons.

Specific examples include (CH ₃ ) Si (OCH ₃ ) ₃ , (CH ₃ ) Si (OC
_{2 H 5) 3, (C} 2 H 5) 2 Si (OCH 3) 2, (nC 6 H 11) Si (OCH 3) 3, (C
₂ H ₅ ) Si (OC ₂ H ₅ ) ₃ , (nC ₁₀ H ₂₁ ) Si (OC ₂ H ₅ ) ₃ , (CH ₂ = CH) Si (O
_{CH 3) 3, Cl (CH} 2) 3 Si (OCH 3) 3, Si (OCH 3) 4, Si (OC 2 H 5) 3 C
_{l, (C 2 H 5)} 2 Si (OC 2 H 5) 2, (C 17 35) Si (OCH 3) 3, Si (OC
_{2 H 5) 4, (C} 6 H 5) Si (OCH 3) 3, Si (OCH 3) 2 Cl 2, (C 6 H 5) 2 Si (OC
_{H 3) 2, (C 6} H 5) (CH 3) Si (OCH 3) 2, (C 6 H 5) Si (OC 2 H 5) 3, (C 6 H
₅ ) ₂ Si (OC ₂ H ₅ ) ₂ , NC (CH ₂ ) ₂ Si (OC ₂ H ₅ ) ₃ , (nC ₃ ) ₇ Si (OC
_{2 H 5) 3, (CH} 3) Si (OC 3 H 7) 3, (C 6 H 5) (CH 2) Si (OC 2 H 5) 3, _{(CH 3) 3 CSi (CH} 3) (OCH 3) 2, (CH 3) 3 CSi (HC (CH 3) 2) (OC
_{H 3) 2, (CH 3} ) 3 CSi (CH 3) (OC 2 H 5) 2, (C 2 H 5) 3 CSi (CH 3) (OC
_{H 3) 2, (CH 3} ) (C 2 H 5) CH-Si (CH 3) (OCH 3) 2, ((CH 3) 2 CHCH 2) S
_{i (OCH 3) 2, C} 2 H 5 C (CH 3) 2 Si (CH 3) (OCH 3) 2, C 2 H 5 C (CH 3) 2 Si
_{(CH 3) (OC 2 H} 5) 2, (CH 3) 3 CSi (OCH 3) 3, (CH 3) 3 CSi (OC
_{2 H 5) 3, (C} 2 H 5) 3 CSi (OC 2 H 5) 3, (CH 3) (C 2 H 5) CHSi (OCH 3) 3
And the like.

Of these, preferred is a branched chain hydrocarbon residue having a secondary or tertiary carbon atom at the α-position of R ⁷ and a carbon number of 3 to 20, particularly R ⁷
Is a silicon compound having a tertiary carbon atom and a branched hydrocarbon residue having 4 to 10 carbon atoms.

The contact conditions of the above-mentioned pre-polymerized or non-pre-polymerized solid catalyst component and the compound represented by the above general formula may be arbitrary as long as the effect of the present invention is recognized,
Generally, the following conditions are preferred. Contact temperature is -50 to
The temperature is about 200 ° C, preferably 0 to 100 ° C. Examples of the contact method include a mechanical method using a rotary ball mill, a vibration mill, a jet mill, a medium stirring / pulverizing machine, and a method of bringing into contact by stirring in the presence of an inert diluent. Examples of the inert diluent used at this time include aliphatic or aromatic hydrocarbons and halohydrocarbons, polysiloxanes (for example, the above-mentioned polymeric silicon compounds), and the like.

The amount of the compound represented by the above general formula used may be any amount as long as the effects of the present invention are recognized, but the general formula is preferably within the following range. The atomic ratio of silicon (silicon / titanium) of the compound represented by the above general formula to the titanium component constituting the solid component containing titanium, magnesium and halogen as essential components is 0.01 to 1000.
Within the range of 0.1 to 100, and preferably within the range of 0.1 to 100.

(Liquid hydrocarbon) As the liquid hydrocarbon used in the method of the present invention, a generally known liquid hydrocarbon is used. Specifically, n-pentane, isopentane, n-hexane,
Linear or branched aliphatic hydrocarbons such as n-heptane, n-octane, isooctane and n-decane, alicyclic hydrocarbons such as cyclohexane and methylcyclohexane, aromatic hydrocarbons such as benzene, toluene and xylene, and kerosene. In addition to these, mixtures of these can also be used.

In the method of the present invention, the liquid hydrocarbon used is preferably a combination of those having a lower boiling point than that of the silicon compound described later which is used at the same time.

(Silicon compound) The silicon compound used in the method of the present invention is represented by the following formula.

(However, R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ each independently represent hydrogen or a hydrocarbon residue, and n is such that the viscosity of this silicon compound is about 1 to 1000 centistokes. The hydrocarbon residue of R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ is usually a hydrocarbon group having about 1 to 10 carbon atoms, and preferably each independently. Selected from hydrogen, lower alkyl or phenyl optionally substituted with lower alkyl.

Specific examples include octamethyltrisiloxane, diphenyloctamethyltetrasiloxane, octaethylcyclotetrasiloxane, hexaphenylcyclotrisiloxane, dimethylpolysiloxane, methylethylpolysiloxane, methylphenylpolysiloxane, 1,3,5 , 7−
Examples thereof include tetramethyl tetrasiloxane, methyl hydrogen polysiloxane, phenyl hydrogen polysiloxane, and the like. The silicon compound used is preferably liquid and has a viscosity of 1 to 1000 centistokes, preferably 5 to
100 centistokes.

The liquid hydrocarbon and the above-mentioned silicon compound may be used in any amounts as long as the effects of the present invention can be observed, but generally, the following ranges are preferable.

The amount of liquid hydrocarbon used is 1 to 100 ml, preferably 2 to 20 ml, per gram of the solid catalyst component.

The amount of the above silicon compound used is preferably in the range of 0.001 to 0.2 gram, and more preferably in the range of 0.01 to 0.1 gram, per gram of the solid catalyst component.

(Drying Method) In the method of the present invention, the solid catalyst component for olefin polymerization containing titanium, magnesium and halogen obtained as described above as essential components is contacted with a liquid hydrocarbon containing the silicon compound or After dispersion, it is dried.

As the drying method, any generally known method can be used, and in many cases, it is preferable to use a dryer. As the type of dryer, material static dryer,
Examples thereof include a material transfer type dryer, a material stirring type dryer, a hot air transfer type dryer, and a cylindrical dryer. The operation can be performed by reducing pressure and / or heating. For example, the pressure is 1 to 700 mmHg, preferably 10 to 200 mmHg, and the temperature is 0 to 100 ° C, preferably 10 to 80 ° C.

The solid component thus obtained is used for the polymerization of olefin in combination with an organoaluminum compound exemplified below as a transition metal component of a Ziegler type catalyst. The term "in combination" as used herein means that, in addition to the solid catalyst component for olefin polymerization obtained by the method of the present invention and the organoaluminum compound, other components are purposely used in combination, for example, known electron donors. Does not interfere.

(Organoaluminum Compound) Specific examples of the organoaluminum compound used in combination with the solid catalyst component obtained by the method of the present invention include R ⁹ _3-n AlX _n or R ¹⁰ _3-m Al (OR ¹¹ ). _m (where R ⁹ and
R ¹⁰ is a hydrocarbon residue or hydrogen atom having about 1 to 20 carbon atoms which may be the same or different, R ¹¹ is a hydrocarbon residue, X is a halogen, and n and m are 0 ≦ n <3 and 0 <m, respectively. <3
Is the number of. ). In particular,
(A) Trialkylaluminum such as trimethylaluminum, triethylaluminum, triisobutylaluminum, trihexylaluminum, trioctylaluminum, tridecylaluminum, etc., (b) diethylaluminum monochloride, diisobutylaluminum monochloride, ethylaluminum sesquichloride, ethyl Alkyl aluminum halides such as aluminum dichloride, (c) diethyl aluminum hydride, diisobutyl aluminum hydride, (d) diethyl aluminum ethoxide, and aluminum alkoxides such as diethyl aluminum phenoxide.

In addition to these organoaluminum compounds (a) to (c), other organometallic compounds such as R ¹² _3-a Al (OR ¹³ ) _a (where 1 ≦ a ≦ 3, R ¹² and R ¹³ are the same or different) An alkylaluminum alkoxide represented by a hydrocarbon residue having about 1 to 20 carbon atoms which may be used can also be used in combination. For example, a combination of triethylaluminum and diethylaluminum ethoxide, a combination of diethylaluminum monochloride and diethylaluminum ethoxide, a combination of ethylaluminum dichloride and ethylaluminum diethoxide, a combination of triethylaluminum and diethylaluminum ethoxide and diethylaluminum chloride. It can be used in combination.

The amount of the organoaluminum compound used is in the range of 0.1 to 1000, preferably 1 to 100, by weight ratio of the organoaluminum compound / transition metal component.

(Use of Catalyst / Polymerization) The solid catalyst component obtained by the method of the present invention, the above-mentioned organoaluminum compound and, if necessary, a third component such as an electron donating compound are used as a catalyst for olefin polymerization. The catalyst is applied not only to ordinary slurry polymerization, but also to liquid phase solventless polymerization, solution polymerization, or gas phase polymerization method which uses substantially no solvent. Further, it is also applied to a system in which continuous polymerization, batch polymerization or preliminary polymerization is carried out. As a polymerization solvent in the case of slurry polymerization, a saturated aliphatic or aromatic hydrocarbon such as hexane, heptane, pentane, cyclohexane, benzene, or toluene is used alone or as a mixture. The polymerization temperature is from room temperature to about 200 ° C., preferably 50 to 150 ° C., and hydrogen can be supplementarily used as a molecular weight regulator at that time. In the slurry polymerization, the amount of the component (A) used is preferably within the range of 0.0001 to 0.1 gram component (A) / Little solvent.

Olefins that polymerize with the above catalyst systems have the general formula R-
CH = CH ₂ (wherein R is a hydrocarbon residue having 1 to 10 hydrogen atoms or carbon atoms, or may have a branch group.) Is represented by. Specifically, there are olefins such as ethylene, propylene, butene-1, pentene-1, hexene-1, and 4-methylpentene-1. Ethylene and propylene are preferred. In these polymerizations, up to 50% by weight, preferably up to 20% by weight, of the olefins can be copolymerized with ethylene, and up to 30% by weight of the olefins, especially ethylene, with respect to propylene. , Can be copolymerized. Copolymerization with other copolymerizable monomers (for example, vinyl acetate, diolefin, etc.) can also be performed.

Experimental Example Example-1 (Synthesis of solid catalyst component) 200 ml of dehydrated and deoxygenated n-heptane was introduced into a flask thoroughly replaced with nitrogen, and then MgCl ₂ was added.
0.4 mol and 0.8 mol of Ti (O-nC ₄ H ₉ ) ₄ were introduced and reacted at 95 ° C for 2 hours. After the completion of the reaction, the temperature was lowered to 40 ° C., and then 48 milliliters of methylhydropolysiloxane (of 20 centistokes) were introduced, followed by a reaction for 3 hours. The resulting solid component was washed with n-heptane.

Then, 50 milliliters of sufficiently purified n-heptane was introduced into a flask which had been sufficiently replaced with nitrogen, and 0.24 mol of the solid component synthesized above in terms of Mg atom was introduced. Then n-
Mix 30 milliliters of heptane with 0.4 mol of SiCl ₄
The mixture was introduced into the flask at 30 ° C for 30 minutes and reacted at 70 ° C for 3 hours. After the completion of the reaction, the resultant was washed with n-heptane. Then n-
25 ml of heptane was mixed with 0.024 mol of phthalic acid chloride and introduced into the flask at 70 ° C for 30 minutes.
And reacted for 1 hour.

After the completion of the reaction, the resultant was washed with n-heptane. Then SiCl ₄
16 milliliters were introduced and the reaction was carried out at 80 ° C for 6 hours. After completion of the reaction, it was thoroughly washed with n-heptane. The titanium content of this product was 1.86 weight percent.

Then an internal volume of 1.5 with stirring and temperature control
Into a stainless steel stirring tank of a liter, 500 ml of sufficiently dehydrated and deoxidized n-heptane, 2.2 g of triethylaluminum, and 20 g of the solid component obtained above were introduced. The temperature in the stirring tank was adjusted to 20 ° C., propylene was introduced at a constant rate, and propylene was polymerized for 30 minutes. After the completion of the polymerization, it was thoroughly washed with n-heptane. A portion was taken out and examined for the amount of propylene polymerized. As a result, the amount of prepolymerized propylene was 1.09 g per 1 g of the solid component.

50 milliliters of sufficiently purified n-heptane was introduced into a flask thoroughly replaced with nitrogen, then 5 g of the prepolymerized component obtained above was introduced, and then (CH ₃ ) ₃ CSi (CH ₃ ) (OCH
₃ ) ₂ was introduced at 0.16 milliliter and contacted at 30 ° C. for 2 hours. After the contact was completed, it was thoroughly washed with n-heptane.

Then 0.6 g of triethylaluminum was introduced, 3
Contact was performed at 0 ° C. for 2 hours. After the contact was completed, it was thoroughly washed with n-heptane. Then (CH ₃ ) ₃ CSi (CH ₃ ) (OCH ₃ ) ₂ was added to 0.16
Milliliter was introduced and contact was performed at 30 ° C. for 2 hours. After the completion of contact, the solid catalyst component was sufficiently washed with n-heptane to obtain a solid catalyst component.

(Drying of Solid Catalyst Component) 4.5 g of the solid catalyst component obtained above, 30 milliliters of n-heptane, and 0.23 g of dimethylpolysiloxane (made of 100 centistokes) were introduced into a thoroughly washed and purified 0.5 l flask. Raise the temperature to 50 ° C and stir gently (100 rp while flowing purified nitrogen gas).
m) dried for 2 hours. As a result, the heptane content was 0.5% by weight and the dimethylpolysiloxane content was 5.0% by weight. When the particle size distribution of the dried solid catalyst component was examined, it was as shown in Table-1.

[Polymerization of propylene]

Into a stainless steel autoclave with an internal volume of 1.5 liters equipped with a stirring and temperature control device, 500 milliliters of fully dehydrated and deoxygenated n-heptane, 125 milligrams of triethylaluminum and the polymer prepolymerized with the components prepared above were removed. 15 mg was introduced as an ingredient.

Then, introduce 60 milliliters of hydrogen, raise the temperature and pressure,
Polymerization was carried out under the conditions of polymerization pressure = 5 kg / cm ² G, polymerization temperature = 75 ° C., and polymerization time = 2 hours. After the polymerization was completed, the obtained polymer slurry was separated by filtration and the polymer was dried. As a result, 169.8 g of polymer was obtained. From one filtrate, 0.37 g of polymer was obtained. From the boiling heptane extraction test, the total product II (hereinafter abbreviated as TI.I) was 99.1% by weight, MFR = 1.2 g / 10 min, polymer bulk specific gravity = 0.48.
The g / cc and polymer particle size distribution are shown in Table 1.

Comparative Example-1 A catalyst component was synthesized in exactly the same manner as in Example-1, and was dried in the same manner as in Example-1 except that the silicon compound was not used during drying. The particle size distribution of the solid catalyst component is shown in Table-1A. The polymerization of propylene was carried out in exactly the same manner. 13
5.6 grams of polymer were obtained, TI.I = 98.9 weight percent, MFR = 1.9 g / 10 min, polymer bulk specific gravity = 0.46 g / cc, polymer particle size distribution is shown in Table-1B.

Examples-2 to 4 Solid catalyst components were synthesized in the same manner as in Example-1, and were the same as in Example-1, except that the type and amount of the silicon compound used during drying were changed as shown in Table-2. Dried.
The results are shown in Table-2. The polymerization was also carried out in exactly the same manner. The results are shown in Table-3A and Table-3B.

Example-5 (Production of solid catalyst component) 75 ml of degassed and purified n-heptane was placed in a 1-liter flask sufficiently replaced with nitrogen, and anhydrous MgCl ₂ (crushed with a ball mill for 24 hours) ) 1
0 g, Ti (O-nC ₄ H ₉ ) ₄ 10 milliliter and AlCl ₃
0.5 g was introduced and reacted at 70 ° C. for 30 minutes. Then
A mixture of 5.4 milliliters of n-butanol and 5.4 milliliters of n-heptane was introduced through a spray nozzle for 5 seconds so as to form droplets of 140 μm, and reacted at 70 ° C. for 1 hour. 2.3 ml of TiCl ₄ was introduced therein and reacted at 70 ° C. for 1 hour. Then, 9 milliliters of methylhydrogen polysiloxane was introduced and reacted at 70 ° C. for 2 hours. After completion of the reaction, it was thoroughly washed with n-heptane to obtain a solid catalyst component.

(Drying) Into a flask purified in the same manner as in Example 1, 5 g of the above solid catalyst component was introduced, 50 milliliter of n-hexane and 0.1 g of polymethylphenylsilicone (20 cm Stokes) were introduced, and 60 The mixture was heated to 0 ° C. and dried under a nitrogen atmosphere for 3 hours. As a result, the hexane content is
0.3% by weight, polymethylphenyl silicone was 2.1% by weight. When the particle size distribution of the dried solid catalyst component was examined, it was as shown in Table-4.

(Polymerization of ethylene) In a stainless steel autoclave having an internal volume of 1.5 liter and equipped with a stirrer and a temperature controller, vacuum-ethylene substitution was repeated several times, and then dehydrated and deoxygenated sufficiently.
800 milliliters of heptane were introduced, followed by 100 milligrams of triethylaluminum and 5 milligrams of the solid catalyst component synthesized above.

The temperature was raised to 85 ° C., hydrogen was introduced at a partial pressure of 4 kg / cm ² , ethylene was introduced at 5 kg / cm ² , and the total pressure was adjusted to 9 kg / cm ² G. Polymerization was carried out for 3 hours. These conditions were kept constant during the polymerization. However, the pressure that decreases as the polymerization progresses is
A constant pressure was maintained by introducing only ethylene. After completion of the polymerization, ethylene and hydrogen were purged, the contents were taken out from the autoclave, the polymer slurry was filtered, and dried in a vacuum dryer for one day. 231 grams of polymer were obtained. For each gram of solid catalyst component, 46,200 grams of polymer (PE) will be obtained. [Yield to catalyst (g · PE / g catalyst component) = 46,200]. When the melt flow rate (MFR) of this polymer was measured, it was 4.1 (g / 10 minutes). The average particle size of the polymer was 945 microns and the bulk density of the polymer was 0.36 g / cc. The particle size distribution of the obtained polymer is shown in Table 4A and Table 4B.

Comparative example-2 In Example-5, it dried like Example-5 except not using a silicon compound at the time of drying. The particle size distribution of the solid catalyst component is shown in Table-4A. The polymerization of propylene was carried out in exactly the same manner. 204 grams of polymer were obtained, MFR = 4.5 g / 10 min, polymer average particle size = 968 microns, polymer bulk specific gravity = 0.34 (g / cc). The particle size distribution of the polymer is shown in Table-4B.

[Brief description of drawings]

FIG. 1 is intended to help the understanding of the technical content of the present invention regarding the Ziegler catalyst.

Claims (1)

(57) [Claims] 1. A solid catalyst component for olefin polymerization containing tetravalent titanium, magnesium and halogen as essential components, a silicon compound of the following formula: (However, R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ each independently represent hydrogen or a hydrocarbon residue, and n is such that the viscosity of this silicon compound is about 1 to 1000 centistokes. A solid catalyst component for olefin polymerization characterized by comprising contacting with or dispersing in a liquid hydrocarbon, and then drying.