JP2719963B2 - α-Olefin polymerization catalyst - Google Patents

Description

Description: TECHNICAL FIELD The present invention relates to an α-olefin polymerization catalyst.

2. Description of the Related Art When a poly-α-olefin is produced using a catalyst component containing magnesium, titanium, chlorine and an electron donating compound, a poly-α-olefin having a Si—O—C bond together with an organoaluminum compound, or a compound represented by the general formula SiR ¹ R ² _n (OR ³ ) _3-n (n = 0 to 2)
It is known that the use of an organosilicon compound represented by the formula improves the stereoregularity of the resulting polymer (for example, JP-A-54-94690, JP-A-56-36203, JP-A-57-63310,
Nos. 58-83016 and 62-11705).

However, contrary to the improvement in stereoregularity, the polymerization activity may be reduced to half or less as compared with the case where the organosilicon compound is not used. Depends on the type. In general, silicon compounds having an aromatic group are known to exhibit good performance in the polymerization of α-olefins, but silicon compounds having an aromatic group may be harmful depending on the purpose of use of the polymer. .

Problems to be Solved by the Invention The present invention is less harmful even if contained in a polymer, an organosilicon compound having no aromatic group,
It is an object of the present invention to provide an α-olefin polymerization catalyst containing, as a component, an organosilicon compound having performance equal to or higher than that of an aromatic group-containing organosilicon compound.

Means for Solving the Problems In general, it is considered that there are two types of α-olefin polymerization catalysts, an active species for producing an isotactic polyolefin and an active species for producing an atactic polyolefin. The polymerization activity (R ₁ ) of the isotactic polyolefin and the polymerization activity (R _A ) of the atactic polyolefin are calculated using the total polymerization activity (R _T ) and stereoregularity (HI: heptane-insoluble content,%) as follows. It is expressed by an equation.

The present inventors performed polymerization of an α-olefin by using a dimethoxy group-containing silane compound in combination with a metal oxide, a catalyst component containing magnesium, titanium, a halogen and an electron donating compound, and an organometallic compound, to obtain R ₁ and R _a and a result of extensive studies the relationship between the properties of the silane compounds, 230 to 350
体積 It has a volume of ³ and the electron density of oxygen of methoxy group is
By using a dimethoxy group-containing silane compound of 0.690 to 0.740 AU, it has been found that a poly-α-olefin having high activity and high stereoregularity equivalent to or higher than an organic silicon compound having an aromatic group can be produced, and completed.

SUMMARY OF THE INVENTION That is, the gist of the present invention is that a solid obtained by contacting (A) (1) a metal oxide, (2) a magnesium compound and (3) an alkoxy group-containing compound is contacted with (4) a halogen-containing alcohol. (5) an electron-donating compound and (6) a solid component obtained by contacting with a tetravalent titanium halide; (B) a general formula R _n AlX _{3-n wherein} R is an alkyl group or aryl A group X represents a halogen atom, an alkoxy group or a hydrogen atom, and n is an arbitrary number in the range of 1 ≦ n ≦ 3], and (C) a general formula R ¹ R ² Si ( OCH ₃ ) ₂ [where R ¹ and R ² are the same or different and are each an aliphatic hydrocarbon group having 4 to 6 carbon atoms, and the total number of carbon atoms of R ¹ and R ² is 9 to 12; Represented by] the volume calculated by quantum chemistry calculation 230～350A ^3, also the electron density of oxygen atoms in the methoxy group is .690-0.740 A.
U. (atomic unit), a dimethoxy group-containing run compound.

Solid Catalyst Component The solid catalyst component (hereinafter, referred to as component A), which is one component of the catalyst of the present invention, comprises a metal oxide, a magnesium compound, an alkoxy group-containing compound, a halogen-containing alcohol, a titanium compound, and an electron-donating compound. It is prepared by contact.

(1) Metal compound The metal oxide used in the present invention is a compound of the Periodic Table II of the Elements.
An oxide of an element selected from the group of group-Group IV element, To illustrate _{them, B 2 O 3, MgO,} Al 2 O 3, SiO 2, Ca
O, TiO ₂ , ZnO, ZrO ₂ , SnO ₂ , BaO, ThO _{2 and the} like. Among them, B ₂ O ₃ , MgO, Al ₂ O ₃ , SiO ₂ , TiO ₂ , Zr
O ₂ is desirable, and SiO ₂ is particularly desirable. Further, composite oxides containing these metal oxides, for example, SiO ₂ -MgO, SiO ₂ -Al ₂
O ₃ , SiO ₂ -TiO ₂ , SiO ₂ -V ₂ O ₅ , SiO ₂ -Cr ₂ O ₃ , SiO ₂ -TiO
_2- MgO or the like may also be used.

These metal oxides are usually in the form of powder. The shape such as the size and shape of the powder often affects the shape of the obtained olefin polymer, and thus it is desirable to appropriately adjust the shape. It is desirable that the metal oxide be fired at as high a temperature as possible and handled so as not to come into direct contact with the atmosphere, for the purpose of removing poisoning substances during use.

(2) Magnesium compound The magnesium compound is represented by the general formula, MgR ¹ R ² . In the formula, R ¹ and R ² are the same or different hydrocarbon groups,
More specifically, the hydrocarbon group for R ¹ and R ² is an alkyl group having 1 to 20 carbon atoms, a cycloalkyl group, an aryl group, and an aralkyl group.

Specific examples of these compounds are shown below.In the chemical formula, Me: methyl, Et: ethyl, Pr: propyl, Bu: butyl,
He: Hexyl, Oct: Octyl, Ph: Phenyl, cyHe: Cyclohexyl.

MgMe ₂ , MgEt ₂ , Mg-Pr ₂ , MgBu ₂ , MgHe ₂ , MgOct ₂ , MgE
tBu, MgPh _2, MgcyHe _2.

Further, as the magnesium compound, a complex with an organic compound of a metal (M) of Group II or Group IIIa of the periodic table can also be used. The complex is represented by the general formula MgR ¹ R ² · n (MR ³ _m ). Examples of the metal include aluminum, zinc, and calcium, and R ³ is an alkyl group having 1 to 12 carbon atoms, a cycloalkyl group, an aryl group, or an aralkyl group.
M represents the valence of the metal M, and n represents a number of 0.1 to 10. M
Specific examples of the compound represented by R ³ _m include AlMe ₃ , AlEt
_{3, Ali-Bu 3, AlPh} 3, ZnMe 2, ZnEt 2, ZnBu 2, ZnPh 2, CaE
t ₂ , CaPh _{2 and the} like.

(3) an alkoxy group-containing compound of the general formula X _n M (OR) _mn wherein X is a hydrogen atom, a hydrocarbon group having 1 to 20 carbon atoms, M is a boron, carbon, aluminum, silicon or phosphorus atom,
R is a hydrocarbon group having 1 to 20 carbon atoms, m is a valence of M, m
> N ≧ 0. ] Is contacted. Examples of the hydrocarbon represented by X and R in the general formula of the alkoxy group-containing compound include methyl (Me), ethyl (Et), propyl (P
r), an alkyl group such as i-propyl (i-Pr), butyl (Bu), i-butyl (i-Bu), hexyl (He), octyl (Oct), and a cyclo group such as cyclohexyl (cyHe) and methylcyclohexyl. Alkyl group, allyl, propenyl,
Alkenyl groups such as butenyl, phenyl (Ph), tolyl,
And aryl groups such as xylyl and aralkyl groups such as phenethyl and 3-phenylpropyl. Among these, an alkyl group having 1 to 10 carbon atoms is particularly desirable. Hereinafter, specific examples of the alkoxy group-containing compound will be described.

C M is contained in the compound formula C (OR) ₄ in the case of carbon _{(OMe) 4, C (OEt} ) 4, C (OPr) 4, C (O
_{Bu) 4, C (Oi-} Bu) 4, C (OHe) 4, C (OOct) 4: Formula XC (OR) HC contained in the _{3 (OMe) 3, HC (} OEt) 3, HC (OPr) 3 , HC (OBu) ₃ , HC (OBu
Ph) ₃ , HC (OPh) ₃ : MeC (OMe) ₃ , MeC (OEt) ₃ , EtO (OMe) ₃ , E
tO (OEt) ₃ , cyHeC (OEt) ₃ , PhC (OMe) ₃ , PhC (OEt) ₃ : Formula X ₂ C
(OR) ₂ contained MeCH (OMe) ₂ , CH ₃ CH (OEt) ₂ , CH ₂ (OM
e) ₂ , CH ₂ (OEt) ₂ , PhCH (OEt) ₂ .

Compound where M is silicon Si (OMe) ₄ , Si (OEt) ₄ , Si (OB) contained in formula Si (OR) ₄
u) ₄ , Si (Oi-Bu) ₄ , Si (OHe) ₄ , Si (OOct) ₄ , Si (OPh) ₄ : Formula
HSi (OEt) ₃ , HSi (OBu) ₃ , HSi (OH) contained in XSi (OR) ₃
e) ₃ , HSi (OPh) ₃ ; MeSi (OMe) ₃ , MeSi (OEt) ₃ , MeSi (OB
u) ₃ , EtSi (OEt) ₃ , PhSi (OEt) ₃ , EtSi (OPh) ₃ : Formula X ₂ Si (O
R) ₂ contained in Me ₂ Si (OMe) ₂ , Me ₂ Si (OEt) ₂ , Et ₂ Si (OE
t) ₂ ; Me ₃ SiOMe, Me ₃ SiOEt, Me ₃ SiOB contained in X ₃ SiOR
u, Me ₃ SiOPh, Et ₃ SiOEt, Ph ₃ SiOEt.

B where M is contained in the compound formula B (OR) ₃ in the case of boron _{(OEt) 3, B (OBu} ) 3, B (OHe) 3, B (O
Ph) ₃ .

Compound when M is aluminum Al (OMe) ₃ , Al (OEt) ₃ , Al (OP) contained in formula Al (OR) ₃
r) ₃ , Al (Oi-Pr) ₃ , Al (OBu) ₃ , Al (Ot-Bu) ₃ , Al (OHe) ₃ , A
l (OPh) ₃ .

Compound when M is phosphorus P (OMe) ₃ , P (OEt) ₃ , P (OBu) ₃ , P (Oe) ₃ contained in formula P (OR) ₃
He) ₃ , P (OPh) ₃ .

(4) Halogen-containing alcohol As the halogen-containing alcohol, any one or two or more hydrogen atoms other than hydroxyl groups in a mono- or polyhydric alcohol having one or more hydroxyl groups in one molecule are halogen atoms. A substituted compound is meant. Examples of the halogen atom include chlorine, bromine, iodine and fluorine atoms, and a chlorine atom is preferable.

Illustrating those compounds are 2-chloroethanol,
1-chloro-2-propanol, 3-chloro-1-propanol, 1-chloro-2-methyl-2-propanol, 4-chloro-1-butanol, 5-chloro-1-pentanol, 6-chloro-1 -Hexanol, 3-chloro-1,2-propanediol, 2-chlorocyclohexanol, 4-chlorobenzhydrol, (m, o, p) -chlorobenzyl alcohol, 4-chlorocatechol, 4-
Chlor- (m, o) -cresol, 6-chloro- (m, o)-
Cresol, 4-chloro-3,5-dimethylphenol,
Chlorohydroquinone, 2-benzyl-4-chlorophenol, 4-chloro-1-naphthol, (m, o, p) -chlorophenol, p-chloro-α-methylbenzyl alcohol, 2-chloro-4-phenylphenol, 6-chlorothymol, 4-chlororesorcin, 2-bromoethanol, 3-bromo-1-propanol, 1-bromo-
2-propanol, 1-bromo-2-butanol, 2-
Brom-p-cresol, 1-bromo-2-naphthol, 6-bromo-2-naphthol, (m, o, p) -bromophenol, 4-bromoresorcin, (m, o, p) -fluorophenol, p -Iodophenol: 2,2-dichloroethanol, 2,3-dichloro-1-propanol, 1,3-dichloro-2-propanol, 3-chloro-1- (α-chloromethyl) -1-propanol, 2 , 3-Dibromo-1
-Propanol, 1,3-dibromo-2-propanol,
2,4-dibromophenol, 2,4-dibromo-1-naphthol: 2,2,2-trichloroethanol, 1,1,1-trichloro-2-propanol, β, β, β-trichloro-tert
-Butanol, 2,3,4-trichlorophenol, 2,4,5-
Trichlorophenol, 2,4,6-trichlorophenol, 2,4,6-tribromophenol, 2,3,5-tribromo-2-toboxytoluene, 2,3,5-tribromo-4-
Toviroxytoluene, 2,2,2-trifluoroethanol, α, α, α-trifluoro-m-cresol, 2,4,
6-triiodophenol: 2,3,4,6-tetrachlorophenol, terachlorhydroquinone, tetrachlorobisphenol A, tetrabromobisphenol A, 2,2,
Examples include 3,3-tetrafluoro-1-propanol, 2,3,5,6-tetrafluorophenol, tetrafluororesorcin and the like.

(5) Electron-donating compound The electron-donating compound is selected from carboxylic acids, carboxylic anhydrides, carboxylic esters, carboxylic halides, alcohols, and ethers.

Specific examples of carboxylic acids include aliphatic monocarboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, caproic acid, pivalic acid, acrylic acid, methacrylic acid, crotonic acid, malonic acid, and succinic acid. , Glutaric acid, adipic acid, sebacic acid, maleic acid, aliphatic dicarboxylic acids such as fumaric acid, aliphatic oxycarboxylic acids such as tartaric acid,
Cyclohexane monocarboxylic acid, cyclohexene monocarboxylic acid, cis-1,2-cyclohexane dicarboxylic acid,
Aromatic carboxylic acids such as cis-4-methylcyclohexene-1,2-dicarboxylic acid, aromatic monocarboxylic acids such as benzoic acid, toluic acid, anisic acid, p-tert-butyl benzoic acid, naphthoic acid, and cinnamic acid Carboxylic acid, phthalic acid, isophthalic acid,
Aromatic polycarboxylic acids such as terephthalic acid, naphthalic acid, trimellitic acid, hemimellitic acid, trimesic acid, pyromellitic acid, and melitic acid are exemplified.

As the carboxylic acid anhydride, the acid anhydrides of the above carboxylic acids can be used.

As the carboxylic acid ester, mono- or multi-value esters of the above carboxylic acids can be used. Specific examples thereof include butyl formate, ethyl acetate, butyl acetate, isobutyl isobutylate, propyl pivalate, isobutyl pivalate, and acrylic. Ethyl acrylate, methyl methacrylate, ethyl methacrylate, isobutyl methacrylate, diethyl malonate, diisobutyl malonate, diethyl succinate,
Dibutyl succinate, diisobutyl succinate, diethyl glutarate, dibutyl glutarate, diisobutyl glutarate, diisobutyl adipate, dibutyl sebacate, diethyl maleate, dibutyl maleate, diisobutyl maleate, monomethyl fumarate, diethyl fumarate, fumarate Diisobutyl acid, diethyl tartrate, dibutyl tartrate, diisobutyl tartrate, ethyl cyclohexanecarboxylate, methyl benzoate, ethyl benzoate, methyl p-toluate, ethyl p-tert-butylbenzoate, ethyl p-anisate, α-naphthoate Ethyl acrylate, isobutyl α-naphthoate, ethyl cinnamate, monomethyl phthalate, monobutyl phthalate, dibutyl phthalate, diisobutyl phthalate, dihexyl phthalate, dioctyl phthalate, di-2-ethyl phthalate Xyl, diallyl phthalate, diphenyl phthalate, diethyl isophthalate, diisobutyl isophthalate, diethyl terephthalate, dibutyl terephthalate, diethyl naphthalate, dibutyl naphthalate, triethyl trimellitate, tributyl trimellitate, tetramethyl pyromellitate, tetramethyl pyromellitate And tetrabutyl pyromellitate.

As the carboxylic acid halide, acid halides of the above carboxylic acids can be used, and specific examples thereof include acetic acid chloride, acetic acid bromide, acetic acid iodide, propionic acid chloride, butyric acid chloride, butyric acid promide, butyric acid iodide, and pivalin. Acid chloride, pivalic acid bromide, acrylic acid chloride, acrylic acid bromide, acrylic acid iodide, methacrylic acid chloride,
Methacrylic acid bromide, methacrylic acid iodide, crotonic acid chloride, malonic acid chloride, malonic acid bromide, succinic acid chloride, succinic acid bromide, glutaric acid chloride, glutaric acid bromide, adipic acid chloride,
Adipic acid bromide, sebacic acid chloride, sebacic acid bromide, maleic acid chloride, maleic acid bromide,
Fumaric acid chloride, fumaric acid bromide, tartaric acid chloride, tartaric acid bromide, cyclohexanecarboxylic acid chloride, cyclohexanecarboxylic acid bromide, 1-cyclohexenecarboxylic acid chloride, cis-4-methylcyclohexenecarboxylic acid chloride, cis-4-methylcyclohexenecarboxylic acid bromide Benzoyl chloride, benzoyl bromide, p-toluic acid chloride, p-toluic acid bromide, p-anisic acid chloride, p-anisic acid bromide,
α-naphthoic acid chloride, cinnamate chloride, cinnamate bromide, phthalic dichloride, phthalic dibromide,
Examples include isophthalic acid dichloride, isophthalic acid dibromide, terephthalic acid dichloride, isophthalic acid dibromide, terephthalic acid dichloride, and naphthalic acid dichloride. Further, monoalkyl halides of dicarboxylic acids such as adipic acid monomethyl chloride, maleic acid monoethyl chloride, maleic acid monomethyl chloride and phthalic acid butyl chloride can also be used.

Alcohols are represented by the general formula ROH. In the formula, R is an alkyl, alkenyl, cycloalkyl, aryl, aralkyl having 1 to 12 carbon atoms. Specific examples thereof include methanol, ethanol, propanol, isopropanol, butanol, isobutanol, pentanol, hexanol, octanol, 2-ethylhexanol, cyclohexanol, benzyl alcohol,
Allyl alcohol, phenol, cresol, xylenol, ethylphenol, isopropylphenol, p
-Tert-butylphenol, n-octylphenol and the like. Ethers represented by the general formula ROR ^1. In the formula, R and R ¹ are alkyl having 1 to 12 carbons,
Alkenyl, cycloalkyl, aryl, aralkyl, wherein R and R ¹ may be the same or different. Specific examples thereof include diethyl ether, diisopropyl ether, dibutyl ether, diisobutyl ether, diisoamyl ether, di-2-ethylhexyl ether, diallyl ether, ethyl allyl ether, butyl allyl ether, diphenyl ether, anisole, and ethylphenyl ether. .

(6) Titanium compound The titanium compound is a halide of tetravalent titanium, and examples thereof include titanium tetrachloride, titanium tetrabromide, trichloroethoxytitanium, trichlorobutoxytitanium, dichlorodiethoxytitanium, and dichlorodibutoxytitanium. , Dichlorodiphenoxytitanium, chlorotriethoxytitanium, chlorotributoxytitanium and the like. Among these, titanium tetrachloride, trichloroethoxytitanium, dichlorodibutoxytitanium, dichlorodiphenoxytitanium and the like are desirable, and titanium tetrachloride is particularly desirable.

The contact with the components (1) to (6) is performed by mixing and stirring or mechanically co-milling in the presence or absence of an inert medium. The contact can be performed under heating at 4 to 150 ° C.

As the inert medium, saturated aliphatic hydrocarbons such as hexane, heptane and octane, saturated alicyclic hydrocarbons such as cyclopentane and cyclohexane, and aromatic hydrocarbons such as benzene, toluene and xylene can be used.

As a specific example of the method for preparing the component A in the present invention, a solid obtained by contacting a metal oxide, a magnesium compound and an alkoxy group-containing compound as disclosed in JP-A-62-7706, This is a method of contacting with a halogen-containing alcohol and further contacting with an electron donating compound and a titanium compound.

The component A is prepared as described above, and the component A may be washed with the above-mentioned inert medium, if necessary, and further dried.

The component A may further contain an olefin polymer formed in the component A upon contact with an olefin in the presence of an organoaluminum compound. The organoaluminum compound is selected from the below-mentioned organometallic compounds which are one component of the catalyst of the present invention.

As the olefin, propylene other than ethylene, 1-
Alpha-olefins such as butene, 1-hexene, 4-methyl-1-pentene can be used. Contact with the olefin is
It is desirable to carry out in the presence of the above-mentioned inert medium. Contact is
Usually, it is carried out at a temperature of 100 ° C. or less, preferably -10 to + 50 ° C. The amount of the olefin polymer contained in the component A is usually 0.1 to 100 g per 1 g of the component A.

The contact between the component A and the olefin may cause the electron donating compound to be present together with the organoaluminum compound. The electron donating compound is selected from the compounds used when preparing component A. Component A in contact with the olefin can be optionally washed with the inert medium described above,
It can be further dried.

Organoaluminum Compound Organoaluminum compound (hereinafter referred to as component B)
General formula R _n AlX _3-n (where R represents an alkyl group or an aryl group, X represents a halogen atom, an alkoxy group or a hydrogen atom, and n is an arbitrary number in the range of 1 ≦ n ≦ 3). Such as trialkylaluminum, dialkylaluminum monohalide, monoalkylaluminum dihalide, alkylaluminum sesquihalide, dialkylaluminum monoalkoxide and dialkylaluminum monohydride, having 1 to 18 carbon atoms, preferably carbon number Particularly preferred are 2 to 6 alkyl aluminum compounds or mixtures or complex compounds thereof. Specifically, trimethylaluminum, triethylaluminum, tripropylaluminum, triisobutylaluminum, trialkylaluminum such as trihexylaluminum, dimethylaluminum chloride, diethylaluminum chloride, diethylaluminum bromide, diethylaluminum iodide, diisobutylaluminum chloride and the like Dialkylaluminum monohalide, methylaluminum dichloride, ethylaluminum dichloride, methylaluminum dibromide, ethylaluminum dibromide,
Monoalkylaluminum dihalides such as ethylaluminum diiodide and isobutylaluminum dichloride, alkylaluminum sesquihalides such as ethylaluminum sesquichloride, dimethylaluminum methoxide, diethylaluminum ethoxide, diethylaluminum phenoxide, dipropylaluminum ethoxide, diisobutylaluminum Ethoxide,
Dialkyl aluminum monoalkoxides such as diisobutyl aluminum phenoxide, dimethyl aluminum hydride, diethyl aluminum hydride,
And dialkylaluminum hydrides such as dipropylaluminum hydride and diisobutylaluminum hydride. Among these, trialkylaluminums, particularly triethylaluminum and triisobutylaluminum, are desirable. Further, these trialkylaluminums are other organoaluminum compounds, for example, industrially available diethylaluminum chloride, ethylaluminum dichloride, ethylaluminum sesquichloride, diethylaluminum ethoxide, diethylaluminum hydride or mixtures or complex compounds thereof Etc. can be used in combination.

Dimethoxy Group-Containing Silane Compound The dimethoxy group-containing silane compound (hereinafter, referred to as component C) used in the present invention is represented by the general formula R ¹ R ² Si (OCH ₃ ) ₂ and has a molecular weight calculated by quantum chemical calculation. Volume 230 ~ 3
50Å ³ , the electron density of the oxygen atom of the methoxy group is from 0.690 to 0.7
40A.U. (atomic unit).

The quantum chemical calculation is performed by the following method. The volume of a molecule is
MNDO method (semi-empirical molecule) of MOPAC, a molecular orbital method program (purchased from QCPE (Quantum Chemistry Program Exchange Organization), a non-profit institution aiming to disseminate various programs for chemistry at Indiana University, USA) Orbital method) [J. Am. Chem. Soc., Journal of American Chemical Society] 99 , 4899, 4907 (19
77); Ibid., 100 , 3607 (1978)] and Van der W
aals radius [J. Phys. Chem., (Journal of Physical Chemistry) 68, 441-452 (1964)]
The electron density of the oxygen atom of the methoxy group was calculated by the MNDO method of MOPAC.
In addition, DEC company (DIGITAL EQUIPMENT CORPORATIO
N) VAX11 / 785 was used.

R ¹ and R ² in the above general formula of the component C are those having 4 to 6 carbon atoms.
Aliphatic hydrocarbon groups, ie, an alkyl group and an alkenyl group, and preferably an alkyl group.

The component C satisfying the volume and electron density as described above, the total number of carbon atoms in R ¹ and R ² are of 9-12 carbon atoms.

Hereinafter, specific examples of the component C are listed by chemical formulas. In the formula, Me: CH ₃ , Et: C ₂ H ₅ , Pr: C ₃ H ₇ , Bu: C ₄ H ₉ , Pt: C
₅ H ₁₁ and He: C ₆ H ₁₃ are shown.

(T-Bu) [(n-Pr) · Me · CH ] _{Si- (OMe) 2, (t} -Pt) 2 Si
(OMe) ₂ , [(n-Pr) · Me · CH] ₂ Si (OMe) ₂ , [t-Bu · CH
_{2] 2} Si (OMe) _{2, [(Et) (Me) 2 C} · CH 2 ] _{2 Si (OMe) 2, (} n-
He) ₂ Si (OMe) ₂ , [(t-Bu) · C ₂ H ₄ ] ₂ Si (OMe) ₂ , [(E
t) (Me) ₂ C • CH ₂ ] ₂ Si (OMe) ₂ , [(n-Pr) (Me) ₂ C] ₂ Si
(OMe) _{2 and the} like.

The catalyst of the present invention is composed of Component A, Component B and Component C.
1-2,000 gram moles per gram atom, preferably 20-5
00 g mol, component C is 0.001 to 10 per mol of component B.
Mole, preferably 0.01 to 1.0 mole.

Polymerization of α-olefin The catalyst of the present invention is useful as a catalyst for homopolymerization of an α-olefin having 3 to 10 carbon atoms or copolymerization with another monoolefin or a diolefin having 3 to 10 carbon atoms,
In particular, α-olefins having 3 to 6 carbon atoms, such as propylene, 1-brene, 4-methyl-1-pentene, 1-
It shows extremely excellent performance as a catalyst for homopolymerization of hexene or the like or random and block copolymerization with the above-mentioned α-olefin and / or ethylene.

The polymerization reaction may be carried out in a gas phase or in a liquid layer.When polymerization is performed in a liquid layer, inert carbonization of normal butane, isobutane, normal pentane, isopentane, hexane, heptane, octane, cyclohexane, benzene, toluene, xylene, etc. It can be carried out in hydrogen and in liquid monomers. The polymerization temperature is usually in the range of -80C to + 150C, preferably 40 to 120C. The polymerization pressure is, for example, 1 to 60
Adjustment of the molecular weight of the resulting polymer may be effected by the presence of hydrogen or other known molecular weight regulators. In the copolymerization, the amount of the other olefin to be copolymerized with the α-olefin is usually selected up to 30% by weight, especially in the range of 0.3 to 15% by weight, based on the α-olefin. The polymerization reaction by the catalyst system according to the present invention is carried out by a continuous or batch reaction, and the conditions may be those usually used. Further, the copolymerization reaction may be performed in one stage, or may be performed in two or more stages.

Effect of the Invention The use of a silane compound having an aromatic group does not generate a harmful substance that causes a problem, and a polymerization activity and stereoregularity equivalent to or higher than that of a catalyst containing the silane compound having an aromatic group. The catalyst exhibits the following catalytic performance.

Examples The present invention will be specifically described with reference to examples and application examples.
The percentages (%) in the examples are by weight unless otherwise specified.

The heptane-insoluble matter (hereinafter abbreviated as HI), which indicates the proportion of the crystalline polymer in the polymer, is the remaining amount when extracted with boiling n-heptane for 6 hours using an improved Soxhlet extractor.

Example 1 Preparation of Component A A 200 ml flask equipped with a dropping funnel and a stirrer was replaced with nitrogen gas. Add silicon oxide (DA
VISON, trade name G-952) in nitrogen stream at 200 ℃
Baking at 700 ° C. for 5 hours and then 5 g and n
40 ml of heptane were charged. Further, 20 ml of a 20% n-heptane solution of n-butylethyl magnesium (hereinafter referred to as BEM) (trade name, MAGALA BEM, manufactured by Texas Alkyls).
And stirred at 90 ° C. for 1 hour.

After the suspension was cooled to 0 ° C, a solution of 11.2 g of tetraethoxysilane dissolved in 20 ml of n-heptane was dropped from the dropping funnel over 30 minutes. After completion of the dropwise addition, the temperature was raised to 50 ° C. over 2 hours, and stirring was continued at 50 ° C. for 1 hour. After completion of the reaction, the supernatant was removed by decantation, and the resulting solid was washed with 60 ml of n-heptane at room temperature.
Further, the supernatant was removed by decantation. This n
-Washing treatment with heptane was further performed four times.

To the above-mentioned fixation, 50 ml of n-heptane was added to form a suspension, and a solution obtained by dissolving 8.0 g of 2,2,2-trichloroethanol in 10 ml of n-heptane was added thereto from a dropping funnel at 25 ° C. for 15 minutes. Hanged and dropped. After completion of the dropwise addition, stirring was continued at 25 ° C. for 30 minutes. After completion of the reaction, 60 ml of n-
Washing was performed twice with heptane and three times with 60 ml of toluene. When the obtained solid (solid component I) was analyzed, it contained 36.6% of SiO ₂ , 5.1% of magnesium, and 38.5% of chlorine.

To the solid component I obtained above, 10 ml of n-heptane and 40 ml of titanium tetrachloride were added, and the temperature was raised to 90 ° C. to give n-heptane.
0.6 g of di-n-butyl phthalate dissolved in 5 ml was added over 5 minutes. Thereafter, the temperature was raised to 115 ° C., and the reaction was performed for 2 hours. After the temperature was lowered to 90 ° C., the supernatant was removed by decantation, and the mixture was washed twice with 70 ml of n-heptane. Furthermore,
15 ml of n-heptane and 40 ml of titanium tetrachloride were added and reacted at 115 ° C. for 2 hours. After the reaction is completed, the obtained solid substance is
Washing was performed eight times at room temperature with ml of n-hexane. Next, drying was performed at room temperature under reduced pressure for 1 hour to obtain 8.3 g of a catalyst component (component A). Component A contained 3.1% titanium as well as silicon oxide, chlorine and di-n-butyl phthalate.

Polymerization of Propylene In a 1.51 stainless steel autoclave equipped with a stirrer, under a nitrogen gas atmosphere, 12.2 mg of the component A obtained above,
4 ml of a solution containing 0.8 mol of triethylaluminum (hereinafter referred to as TEAL) in n-heptane 11 and 1 ml of a solution containing 0.08 mol of di (t-pentyl) dimethoxysilane in n-heptane 11 are mixed and kept for 5 minutes. I put what I did. Next, 600 ml of hydrogen gas and liquid propylene 11 as a molecular weight controller were injected under pressure, and then the temperature of the reaction system was increased to 70 ° C., and propylene was polymerized for 1 hour. After completion of the polymerization, unreacted propylene was purged to obtain 97.9% HI white polypropylene powder. The polymerization activity (R _T ) of the catalyst is 14.6 kg
/ g · component A. Thus, the polymerization activity (R ₁ ) of isotactic polypropylene is 14.3 kg / g · component A, and the polymerization activity ( _RA ) of atactic polypropylene is 0.3 kg / g ·
Component A was determined.

Further, the volume of di (t-pentyl) dimethoxysilane and the electron density of oxygen atoms of the methoxy group were calculated in accordance with the above, and the results are shown in Table 1 (R ¹ and R ² in the table are represented by the general formula R ¹ R ² Si (OCH ₃ ) _2. The same applies hereinafter. Examples 2 to 3 Example 1 was repeated except that the silane compounds shown in Table 1 were used instead of di (t-pentyl) dimethoxysilane. Propylene was polymerized in the same manner, and the results are shown in Table 1.

Also, calculate the volume of the compound and the electron density,
The results are shown in Table 1.

Comparative Examples 1-4 Propylene was polymerized in the same manner as in Example 1 except that the compounds shown in Table 1 were used as the silane compounds, and the results are shown in Table 1. Table 1 shows the volume of these compounds and the calculated value of the electron density.

Reference Examples 1 and 2 Propylene was polymerized in the same manner as in Example 1 except that a phenyl group-containing compound shown in Table 1 was used as a silane compound. The results are shown in Table 1. Table 1 shows the volume of these compounds and the calculated value of the electron density.

[Brief description of the drawings]

FIG. 1 is a flowchart showing the preparation process of the catalyst of the present invention.

 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Hiroyuki Furuhashi 1-3-1, Nishitsurugaoka, Oi-machi, Iruma-gun, Saitama Prefecture Within Toa Fuel Industry Co., Ltd. (72) Inventor Satoshi Ueki Oimachi, Iruma-gun, Saitama 1-3-1 Nishitsurugaoka Research Institute, Toa Fuel Industry Co., Ltd. (72) Inventor Akira Nakano 1-31-1 Nishitsurugaoka, Oimachi, Iruma-gun, Saitama Prefecture Research Institute, Toa Fuel Industry Co., Ltd. (56) JP-A-2-229806 (JP, A) JP-A-2-283703 (JP, A) JP-A-2-102205 (JP, A) JP-A-2-32106 (JP, A) JP-A-1 JP-A-156305 (JP, A) JP-A-64-33106 (JP, A) JP-A-63-199703 (JP, A) JP-A-62-158703 (JP, A) JP-A-63-223008 (JP, A) ) JP-A-62-201905 (JP A)

Claims (1)

(57) [Claims] 1. A solid obtained by contacting (A) (1) a metal oxide, (2) a magnesium compound and (3) an alkoxy group-containing compound, is brought into contact with (4) a halogen-containing alcohol, and further (5) An electron donating compound and (6) a general formula TiX _n (OR) _{4-n wherein} X is a halogen atom,
R represents a hydrocarbon group, and 0 <n ≦ 4. Solid component obtained by contacting with the titanium compound represented by], (B) the general formula R _n AlX _3-n [where, R represents an alkyl group or an aryl group, X is a halogen atom, an alkoxy group or a hydrogen atom And n is an arbitrary number in the range of 1 ≦ n ≦ 3], and (C) a general formula R ¹ R ² Si (OCH ₃ ) ₂ [where R ¹ and R ² are in each the same or different number 4-6 aliphatic hydrocarbon group having a carbon and the total carbon number of R ¹ and R ² are 9 to 12 amino. Represented by] the volume calculated by quantum chemistry calculation 230～350A ^3, also the electron density of oxygen atoms in the methoxy group is .690-0.740 A.
U. (Atomic unit) dimethoxy group-containing silane compound.