Production of olefin polymers

temperature.

PRODUCTION OF OLEFIN POLYMERS

BACKGROUND OF THE INVENTION Field of the Art

The present invention relates to Ziegler polymerization of olefins. More particularly, the present invention is concerned with Ziegler polymerization of olefins, typically «-olefins of at least 3 carbon atoms, characterized by, among others, the solid catalyst components comprising a transition metal in Ziegler catalysts and the polymerization temperature used which is no lower than 150°C.

Use of the solid catalyst component in accordance with the present invention in Ziegler catalysts as the transition metal component at the temperature will make it possible to produce polymers endowed with improved stereoregularity and broadened molecular weight distribution.

Background of the Invention

The catalysts heretofore proposed for the polymerization of olefins comprising a solid catalyst component containing titanium, magnesium and a halogen as the essential components and an organoaluminum compound (and an electron donor, if desired) have produced highly stereoregular polymers.

Such prior art catalysts are such that their catalyst activity may often be found at a polymerization temperature of 90°C or lower, preferably 80°C or lower.

It has been known in the art that ethylene polymerizes at such a higher temperature as 150 to 250°C similarly at a temperature of 70 to 90°C and that polymerization of ethylene, at such a higher temperature is known to have such preferable characteristics that the polyethylenes produced have a narrower molecular weight distribution or copolymerizability of ethylene with another monomer is improved.

20S1963

It has also been known in the art that propylene will not produce polymers endowed with acceptably high stereoregularity when it is polymerized at such a high temperature as 150°C or higher. One possible reason therefor may be such that the solid structure comprising the titanium component capable of polymerizing propylene into polymers of high stereoregularity is destroyed at a temperature no lower than 150°C, the titanium component is aggromerated or excessively reduced by the organoaluminum component as a co-catalyst, or, when an electron donor is used during polymerization as what is called outside electron donor, it reacts so strongly with the titanium component or with the organoaluminum component at such a higher temperature that the catalyst activity is thus lowered.

Catalysts which are capable of producing highly stereoregular polymers at such a high temperature as no lower than 150°C have, to the best of the present inventors, not been proposed.

It has also been known to use as an organoaluminum component in the Ziegler catalysts organoaluminum compounds which contain a halogen atom. The halogen atom may have such a problem due to its inherent corrosive nature that polyolefins produced therewith can corrode or rust processing machines for the polymers. An organoaluminum component in Ziegler catalysts which is free from a halogen contained therein has heretofore been desired.

SUMMARY OF THE INVENTION

The present invention is based on the discovery that the above problems can be solved by use of a specified solid catalyst component in.Ziegler catalysts.

More particularly, the present invention presents a process for producing c-olefin polymers which comprises contacting at a temperature of 150°C to 300°C an olefin with a catalyst thereby to polymerize the olefin, the catalyst comprising:

CA 02061963 2002-09-18

Component (A) which is a solid catalyst component for Ziegler catalysts, which solid catalyst component is obtained by contacting the following Sub-components (i) to (iii) :

Sub-component (i) which is a solid catalyst component for Ziegler catalysts comprising titanium, magnesium and a halogen as the essential components;

Sub-component (ii) which is a silicon compound represented by a formula ^RlA^{S 1} ( °^r2 ) 4-m-n wherein R¹ indicates a hydrocarbyl group of 1 to 20 carbon atoms, R² which may be the same as or different from R¹ indicates a hydrocarbyl group of 1 to 20 carbon atoms, X indicates a halogen atom, and m and n are each numbers satisfying equations 0 < m <3, 0 < n 1 3 and 0 < (m+n) < 3; and

Sub-component (iii) which is an organometal compound of a metal of the Groups I to III of the Periodic Table; and

Component (B) which is an organoaluminum compound represented by a formula ^r33-P^HP^A1 wherein R³ indicates a hydrocarbyl group of up to 5 carbon atoms and p is a number satisfying an equation D < p < 1;

wherein the mole ratio of the Al in Component (B) to the Ti in Component (A) is equal to or less than 1.

It has now been possible in accordance with the present invention that highly stereoregular olefin polymers are produced at a temperature of 150°C or higher where it would have not been possible to prepare such polymers in yield of a level comparable to that obtained by polymerization at a lower temperature of 80°C or lower using known Ziegler catalysts.

The polymer produced by the present invention is characterized by the fact that they have broader molecular weight distribution than those produced at a lower polymerization temperature of 80°C or lower.

DETAILED DESCRIPTION OF THE INVENTION

[IJ Catalyst

The catalyst of the present invention comprises a combination of specific components (A) and (B). Here, the wording comprises means that the components are not limited only to those mentioned (namely, A and B), and includes co-presence of other components compatible with or suited for the purpose, such as an outside electron donor which is not essential but can be used if desired.

Component (A)

The Component (A) of the catalyst of the present invention is a solid catalyst component for Ziegler catalysts obtained by contacting the Sub-components (i) to (iii) shown below. The contact product of the Subcomponents (i) to (iii) is washed amply with an inert hydrocarbon solvent to form the Component (A). Here, the wording obtained by contacting** means that the components are not limited only to those mentioned, namely (i) to (iii), and includes co-presence of other components suited for the purpose.

Sub-component (i)

Sub-component (i) is a solid component comprising titanium, magnesium and a halogen as the essential components. Here, the wording comprising as the essential components indicates that it can also contain other elements suited for the purpose than the three components mentioned, that these elements can exist in any desired compound suited for the purpose respectively, and also that these elements can also exist in the form mutually bonded together. Solid components containing titanium, magnesium and a halogen are known perse. For example, those as disclosed in Japanese Laid-open Patent Publications Nos. 45688/1978, 3894/1979, 31092/1979,

94591/1979, 118484/1979, 131589/1979,

90510/1980, 90511/1980, 127405/1980,

39483/1979,

75411/1980,

147507/1980, 155003/1980, 18609/1981, 70005/1981,

72001/1981, 86905/1981, 90807/1981, 155206/1981,

3803/1982, 34103/1982, 92007/1982, 121003/1982,

5309/1983, 5310/1983, 5311/1983, 8706/1983, 27732/1983,

32604/1983, 32605/1983, 67703/1983, 117206/1983,

127708/1983, 183708/1983, 183709/1983, 149905/1984 and

149906/1984 may be employed.

As the magnesium compound which is the magnesium source to be used in the present invention, magnesium dihalides, dialkoxymagnesiums, alkoxymagnesium halides, magnesium oxyhalides, dialkylmagnesiums, magnesium oxide, magnesium hydroxide, carboxylates of magensium, etc. are exemplified. Among these magnesium compounds, magnesium dihalides, dialkoxymagnesiums and alkoxymagnesium halides, particularly MgCl₂, are preferred.

As the titanium compound which is the titanium source, compounds represented by the formula Ti(OR⁴)_4-gX_q(wherein R⁴ is a hydrocarbyl group, preferably having about 1 to 10 carbon atoms, X represents a halogen atom and q is an integer of 0 < q < 4) and polymers of a titanium tetraalkoxide.

Specific examples may include;

titanium tetrahalides such as TiCl₄, TiBr₄ and the like;

alkoxytitanium halides such as Ti(OC₂H₅)C1₃,

Ti (OC₂H₅ ) ₂C1₂,

Ti(OC₂H₅)₃Cl,

Ti(O-iC₃H₇)Cl₃,

Ti(O~nC₄Hg)Cl₃,

Ti(O-nC₄H_g)₂Cl₂,

Ti(OC₂H₅)Br₃,

Ti(OC₂H₅)(OC₄H_g)₂Cl,

Ti(O-nC₄H_g)₃Cl,

Ti(O-C₆H₅)Cl₃,

Ti(O-iC₄H_g)₂Cl₂,

Ti(OC₅H₁₁)C1₃,

Tî(OC₆H₁₃)C1₃, and the like;

and titanium tetraalkoxides such as

Ti(OC₂H₅)₄,

Ti (O-iC₃H₇)₄, Ti ( O~nC₃H₇ ) ₄, Ti(O-nC₄H₉)₄, Ti(O-iC₄H₉)₄, Ti ( O-nC₅H_xl ) _{4 f}Ti(O-nC₆H₁₃)₄, Ti ( O-nC_?H₁₅ )₄, Ti (O-nC₀H₁₇)_{4 r}

Ti[OCH₂CH(CH₃}₂]₄,

Ti[OCH₂CH(C₂H₅)C₄H₉]₄Polymers of a those represented by the following formula: r- OR⁷I

R⁵O —k Ti , and the like, titanium tetraalkoxide may include

L OR⁸ wherein, R⁵ - R⁸ represent the same or different hydrocarbyl groups, preferably aliphatic hydrocarbyl group having 1 to 10 carbon atoms or aromatic hydrocarbyl groups, particularly aliphatic hydrocarbyl groups having 2 to 6 carbon atoms, n represents a number of 2 or more, particularly a number up to 20. The value of n should be desirably selected so that the polytitanate itself or as a solution can be provided in a liquid state for the contact step with other components. A suitable n selected in view of ease of handling may be about 2 to 14, preferably 2 to 10. , Specific examples of such polytitanates may include n-butylpolytitanate (n = 2 to 10), hexylpolytitanate (n ~ 2 to 10), n-octylpolytitanate (n = 2 to 10), and the like. Among them, n-butylpolytitanate is preferred.

It is also possible to use, as the titanium compound for the titanium source, a molecular compound obtained by reacting an electron donor as described below with a compound TiX'₄ (where X' represents a halogen). Specific examples may include:

TiCl₄-CH₃COC₂H₅,

TiCl₄-CH₃CO₂C₂H₅,

TiCl₄-C₆H₅NO₂,

TiCl₄-CH₃COCl,

TiCl₄-C₆H₅COCl,

TiCl₄-C₆H₅CO₂C₂H₅,

TiCl₄·C1COC₂H₅,

TiCl₄*C₄H₄O, and the like.

Among these titanium compounds, TiCl₄, Ti(OC₂H₅)₄,

Ti(O-nC₄H_g)₄ , and Ti(O-nC₄H_g)Cl₃ are prefered. Particularly, TiCl₄ and Ti(O-nC₄H₉)₄ are prefered.

As to the halogen source, it is a common practice to supply the halogen from the halide compounds of magnesium and/or titanium as described above, but it can be also supplied from known halogenating agents such as halogen compounds of aluminum, halogen compounds of silicon, halogen compounds of phosphorus, and the like.

The halogen contained in the catalyst components may be fluorine, chlorine, bromine, iodine or a mixture of these, particularly preferably chlorine.

The solid component to be used in the present invention can also include, in addition to the above essential components: a silicon compound such as SiCl₄, CH₃SiCl₃, and the like; a polymeric silicon compound having the structure represented by the following formula:

R

I — Si —O — (wherein R is a hydrocarbyl group having about 1 to 10, preferably about 1 to 6 carbon atoms) and having a viscosity of about 1 centistoke to 100 centistokes, such as methylhydrogenpolysiloxane, ethylhydrogenpolysiloxane, phenylhydrogenpolysiloxane , cyclohexylhydrogenpolysiloxane, 1,1,3,3-tetramethyldisiloxane, 1,3,5,7tetramethylcyclotetrasiloxane, 1, 3 , 5 , 7 , 9 pentamethylcyclopentasiloxane and the like; an aluminum compound such as Al{OiC₃H₇)₃, A1C1₃, AlBr₃, A1(OC₂H₅)₃, A1(OCH₃)₂C1; a boron compound such as B(OCH₃)₃, B(OC₂H₅)₃, B(OC₆H₅)₃; WC1₆ and MoC1₅. These optional compounds may remain in the solid component as the components of silicon, aluminum and boron.

further, in preparing the solid component, use can also be made of an electron donor as what is called an inside donor¹'.

Examples of the electron donor or the inside donor which can be used for preparation of the solid component may include oxygen-containing electron donors such as alcohols, phenols, ketones, aldehydes, carboxylic acids, esters of an organic acid or an inorganic acid, ethers, acid amides, acid anhydrides, and the like; and nitrogencontaining electron donors such as ammonia, amines, nitriles, isocyanates, and the like.

More specifically, there may be included: (a) alcohols having 1 to 18 carbon atoms, such as methanol, ethanol, propanol, pentanol, hexanol, octanol, dodecanol, octadecyl alcohol, benzyl alcohol, phenylethyl alcohol, isopropylbenzyl alcohol and the like? (b) phenols having 6 to 25 carbon atoms which may or may not have an alkyl group, such as phenol, cresol, xylenol, ethylphenol, propylphenol, isopropylphenol, nonylphenol, naphthol and the like; (c) ketones having 3 to 15 carbon atoms, such as acetone, methyl ethyl ketone, methyl isobutyl ketone, acetophenone, benzophenone and the like? (d) aldehydes having 2 to 15 carbon atoms, such as acetaldehyde, propionaldéhyde, octylaldehyde, benzaldehyde,

<img file="CA2061963C_D0001.tif" />

tolualdehyde, naphthaldehyde and the like; (e) organic acid esters having 2 to 20 carbon atoms, such as methyl formate, methyl acetate, ethyl acetate, vinyl acetate, propyl acetate, octyl acetate, cyclohexyl acetate, cellosolve acetate, ethyl propionate, methyl butyrate, ethyl valerate, ethyl stearate, methyl chloroacetate, ethyl dichloroacetate, methyl methacrylate, ethyl crotonate, ethyl cyclohexanecarboxylate, methyl benzoate, ethyl benzoate, propyl benzoate, butyl benzoate, octyl benzoate, cyclohexyl benzoate, phenyl benzoate, benzyl benzoate, methyl toluylate, ethyl toluylate, amyl toluylate, ethyl ethylbenzoate, methyl anisate, ethyl anisate, ethyl ethoxybenzoate, diethyl phthalate, dibutyl phthalate, diheptyl phthalate, /-butyrolactone, α-valerolactone, coumarine, phthalide, ethylene carbonate, cellosolve acetate, cellosolve isobutyrate and cellosolve benzoate, etc.; (f) inorganic acid esters, such as silicates such as ethyl silicate, butyl silicate, phenyl-triethoxysilane, etc.; (g) acid halides having 2 to 15 carbon atoms, such as acetyl chloride, benzoyl chloride, toluyloic chloride, anisic chloride, phthaloyl chloride, phthaloyl isochloride and the like; (h) ethers having 2 to 20 carbon atoms, such as methyl ether, ethyl ether, isopropyl ether, butyl ether, amyl ether, tetrahydrofuran, anisole, diphenyl ether and the like;

(i) acid amides, such as acetic amide, benzoic amide, toluyloic amide and the like; (j) amines, such as monomethylamine , monoethylamine, diethylamine, tributylamine, piperidine, tribenzylamine, aniline, pyridine, picoline, tetramethylethylenediamine and the like; and (k) nitriles, such as acetonitrile, benzonitrile, tolunitrile and the like. One or more of these electron donors can be used in preparing the solid catalyst component. Among them, preferred are organic acid esters and acid halides, particularly preferably phthalic acid esters, phthalic acid halides, and cellosolve acetate.

The amounts of the above respective components used may be at any desired level, so long as the advantages inherent in the present invention can be attained, but, generally speaking, the following ranges are preferred.

The amount of the titanium compound used may be within the range of 1 χ 10⁴ to 1000, preferably 0.01 to 10, in terms of molar ratio relative to the amount of the magnesium compound used. When a compound as the halogen source is used, its amount used may be within the range of 1 x 10“² to 1000, preferably 0.1 to 100, in terms of a molar ratio relative to magnesium used, irrespective of whether the titanium compound and/or the magnesium compound may contain a halogen or not.

The amount of the silicon, aluminum, boron, wolfram or molybdenum compound when used may be within the range of 1 x 10³ to 100, preferably 0.01 to 10, in terms of a molar ratio to the amount of the above magnesium compound used.

The amount of the electron donor compound when used may be within the range of 1 χ 10³ to 10, preferably 0.01 to 5/ in terms of a molar ratio relative to the amount of the above magnesium compound used.

The solid component for preparing the Sub-component (i) may be prepared from the titanium source, the magnesium source and the halogen source, and further optionally other components such as an electron donor according to methods mentioned below.

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

(b) A method in which alumina or magnesia is treated with a phosphorus halide compound, and the product is contacted with a magnesium halide, an electron donor, a titanium halide-containing compound.

(c) A method in which the solid component obtained by contacting a magnesium halide with a titanium tetraalkoxide and a specific polymeric silicon compound

<img file="CA2061963C_D0002.tif" />

is contacted with a titanium halide compound and/or a silicon halide compound.

As the polymeric silicon compound, those represented by the following formula are suitable:

H

I

Si o-)-_nI

R wherein R is a hydrocarbyl group having about 1 to 10 carbon atoms, n is a polymerization degree such that the viscosity of the polymeric silicon compound may be 1 to 100 centistokes.

Among them, methylhydrogenpolysiloxane, 1,3,5,7tetramethylcyclotetrasiloxane, 1,3,5,7,9-pentamethylcyclopentacycloxane, ethylhydrogenpolysiloxane, phenylhydrogenpolysiloxane, and cyclohexylhydrogen polysiloxane are preferred.

(d) A method in which a magnesium compound is dissolved in a titanium tetraalkoxide and an electron donor, and the solid component precipitated from the solution upon addition thereto of a halogenating agent or a titanium halide compound is contacted with a titanium compound. Examples of halogenating agents include silicon halides, aluminium halides, and halogen compounds of phosphorus.

(e) A method in which an organomagnesium compound such as Grignard reagent, etc. is reacted with a halogenating agent, a reducing agent, etc., and then the reaction product is contacted with an electron donor and a titanium compound.

(f) A method in which an alkoxymagnesium compound is contacted with a halogenating agent and/or a titanium compound in the presence or absence of an electron donor.

Among these methods, method (c), (d) and (f) are preferable.

Sub-component (ii)

<img file="CA2061963C_D0003.tif" />

Sub-component (ii) for preparing the Component (A) is a silicon compound expressed by a formula

R^SiR²)^ wherein R¹ is a hydrocarbyl group of 1 to 20 carbon atoms, R² is a hydrocarbyl group of 1 to 20 carbon atoms which is the same as or different from R¹, X is a halogen atom, and m and n are each numbers satisfying equations 0 &lt;m&lt;3, 0 &lt; n &lt; 3 and 0 &lt; (m+n) &lt; 3.

R¹ and R² have 1 to 20, preferably 1 to 10, carbon atoms and may be in a branched or straight configuration, respectively.

X is preferably a chlorine atom at least from an economical point of view.

R² may be an aliphatic hydrocarbyl group, and preferably is a hydrocarbyl group of 1 to 4 carbon atoms.

Specific examples of the silicon compounds may include;

(CH₃)Si(OCH₃)₃, (CH₃)Si(OC₂H₅)₃, (C₂H₅)₂Si(OCH₃)₂, (i-C₃H₇)₂Si(OCH₃)₂ (n-C₆H₁₃)Si(OCH₃)₃, (i-C₃H₇)Si(0C₂H₅)₃, (i-C„H_g)₂Si(OCH₃)2, (C₆H_u)₂Si[OCH₃)₂, (C₆H_u)(CH₃)Si (OCH₃)₂, (θ6®11θ^Η₃)j &gt;

(C₆H_l;l)(CH₃)Si(OCH₃)₂, (C₅H₄)₂Si(OCH₃)₂, (C₅H₄)(CH₃)Si(OCH₃)₂, (C₂H_s)Si(OC₂H₅)₃, (n-Ci_DH2i)Si(°C₂H₅)3,

Cl (CH_Z)₃Si(OCH₃)3,

Si(OCH₃)₄,

Si(OC₂H₅)₃Cl, (C₂H₅)₂Si(OC₂H₅)₂, (^c17H₃₅)Si(OC^H3)₃,

Si(OC₂H_g)₄, (C₆H_s) Si(OCHj)₃,

Si(OCH₃)₂C1₂, (C₆H₅)₂Si(OCH₃)₂, (C₆H₅)(CH₃)Si(OCH₃)₂, (C₆H₅)Si(OC₂H₅)₃, (CgHg)₂Si (OC₂H_g)₂r NC(CH₂)₂Si(OC₂H₅)₃, (C₆H_s)(CH₃)Si(OC₂H₅)₂, (n-C₃H₇)Si(OC₂H₅)₃, (CH₃)Si&lt;OC₃H₇)₃, (C₆H₅){CH₂) Si(OC₂H₅)₃, rS ch₂ ^^^Si(OC₂H₅)₃ , ch₂

Si(CH₃) (OC₂Hg)₂ , ch₂^k'''L''^k^Si(CH₃)(OCH₃)₂ ,

<img file="CA2061963C_D0004.tif" />

<img file="CA2061963C_D0005.tif" />

(CH₃)₃csi(CH₃)(OCH₃)₂, (ch₃)₃csi(HC(CH₃)₂)(OCH₃)₂,

2061063 (CH₃)₃CSi(CH₃)(OC₂H₅}₂, (^C2^H5)3^CSi(^CH3) f ^0CH3)2’ (CH₃)(C₂H₅)CHSi(CH₃)(OCH₃)₂, {(CH₃)₂CHCH₂)₂Si(OCH₃)₂, (C₂H₅)(CH₃)₂CSi(CH₃)(OCH₃)₂, (C₂H₅)(ch₃)₂CSi(CH₃){oc₂h₅)₂, (CH₃)₃CSi(OCH₃)₃, (CH₃)₃CSi(OC₂H₅)₃, (C₂H₅)₃CSi(O^c2H₅)₃, ( CH₃ ) ( C₂H₅ ) CHSi ( OCH₃ ) ₃, (C₂H₅)(CH₃)₂CSi{OCH₃)₃, (C₂H₅)(CH₃)₂CSi{OC₂H₅)_3r (C₂H_g)₃CSi (OC₂H₅) ₃, (CH₃) (C₂H₅)CHSi(OCH₃)₃, ({CH₃)₃C)₂Si(OCH₃)₂.

It is preferable that R¹ has a branch at the carbon atom adjacent to the silicon atom. The branch may preferably be an alkyl group or a cycloalkyl group. More preferably, the carbon atom adjacent to the silicon atom, namely α-carbon atom, is a secondary or tertiary carbon atom in a branched hydrocarbyl group having 3 to 20 carbon atoms. Most preferably, the carbon atom connected with the silicon atom is a tertiary carbon atom in a branched hydrocarbyl group having 4 to 10 carbon atoms. Sub-component (iii)

Sub-component (iii) for preparing a solid catalyst component in accordance with the present invention is an organometal compound of a metal of the Group I to III of the Periodic Table.

Examples of the metals include lithium, magnesium, aluminum and zinc, but aluminum is representable.

The compounds are organometal compounds and thus have at least one organic radical-metal bonding. The organic radical may typically be a hydrocarbyl group of 1 to 20 carbon atoms, preferably 1 to 10 carbon atoms, more preferably 1 to 6 carbon atoms.

The remaining valence of the metal in question other than those satisfied by an organic radical, if any, can be satisfied by a hydrogen atom, a halogen atom, hydrocarbyloxy group of I to 10, preferably 1 to 6, carbon atoms, or the metal itself with an oxygen bridge therebetween such as-O-Al- when the compounds are ch₃ methylalminoxanes.

Specific examples of such organometal compounds may include: (a) organolithium compounds, e.g. methyllithium, n-butyllithium, sec.-butyllithium, tert.-butyllithium and the like; (b) organomagnesium compounds, e.g. diethylmagnesium, ethylbutylmagnesium, dibutylmagnesium, dihexylmagn.esium, hexylethylmagnesium, ethylmagnesiura chloride, ethylmagnesium bromide, butylmagnesium chloride, tert.-butylmagnesium bromide, and the like; (c) organozinc compounds, e.g. diethylzinc, dimethylzinc, dibutylzinc, and the like; (d) organoaluminum compounds, e.g. trimethylaluminum, triethylaluminum, triisobutylaluminum, tri-n-hexylaluminum, diethylaluminum chloride,, diethylaluminum hydride, diethylaluminum ethoxide, ethylaluminum sesquichloride, ethylaluminum dichloride, methylaluminoxane, and the like. Among these, organoaluminum compounds and organozinc compounds, especially the former, are preferable.

The most preferable are organoaluminum compounds and further examples of organoaluminum compounds may be found in the examples of organoaluminum compounds as the Component (B) which will be given hereinbelow, but include:

Al()3'

Al(iC₃H₇)₃,

Al(nC₃H₇)₃,

Al(iC₄H₉)₃,

Al(nC₄H_g)₃,

<img file="CA2061963C_D0006.tif" />

A1(C₅H₁₁)₃,

Al(nCgHj₃)_{3 f}

Al ( CgHj? )_{3 f}

Al (C₁₀H₂₁)₃,

A1{C₂H₅)₂C1,

A1(1C₄H₉)₂C1,

Al(C₂Hg)₂H,

Al(iC₄H₉)₂H,

A1(C₂H₅)₂&lt;^OC₂H₅).

Preparation of the Component (A)

The contacting method and conditions for the Subcomponents (i) to (iii) can be as desired, so long as the advantages inherent in the present invention can be attained, but generally the following conditions are preferred. The contact temperature may be about -50 to 200°C, preferably 0 to 100°C. As the contacting method, there may be employed the mechanical method wherein a rotating ball mill, a vibrating ball mill, a jet mill, a medium stirring pulverizer or the like is used and the method in which contact is effected with stirring under the presence of an inert diluent. As the inert diluent to be used, aliphatic or aromatic hydrocarbons and halohydrocarbons, polysiloxane, etc. may be exemplified.

The contacting order and the contacting time of the Sub-components (i) to (iii) in preparing the component (A) of the present invention may be any desired one, so long as the advantages inherent in the present invention are attained.

Specific orders of such contact may include those as shown below, where the symbol *’+ indicates a contact between the components flanking the symbol, and a washing

<td colspan="2"> or rinsing processing</td><td colspan="3"> can. be interposed between the</td>

<td colspan="2"> contacts.</td><td></td><td></td><td></td>

<td> (a)</td><td> {Sub-component (i) component (iii);</td><td> + Sub-component</td><td> (ii)} +</td><td> Sub-</td>

<td> (b)</td><td> {Sub-component ( i ) component (ii);</td><td> + Sub-component</td><td> (iii)} +</td><td> Sub-</td>

<img file="CA2061963C_D0007.tif" />

<td> (C)</td><td> Sub-component {i) + component (iii)} + component (iii);</td><td> {Sub-component {Sub-component</td><td> (ii) + (ii) +</td><td> {Sub- Sub-</td>

<td> (a)</td><td> {Sub-component (ii) + component (i) ;</td><td> Sub-component</td><td> (iii)} +</td><td> Sub-</td>

<td> (e)</td><td> Sub-component (i) +</td><td> Sub-component</td><td> (ii) +</td><td> Sub-</td>

component (iii) ♦

The quantitative ratio of the Sub-components (i) to (iii) can be any desired one, so long as the advantages inherent in the present invention can be attained, but generally preferred to be within the following ranges.

The quantitative ratio of the Sub-component (i) to (ii) may be within the range of 0.01 to 1000, preferably 0.1 to 100, in terms of the atomic ratio (silicon/titanium) of the silicon of the Sub-component (ii) to the titanium component constituting the Subcomponent (i).

The Sub-component (iii) is used in an amount within the range of 0.01 to 100, preferably 0.1 to 30, in terms of the atomic ratio of the metals {(Sub-component (iii) /titanium(Sub-component (x J ).

Modification of the Component (A) can be applied provided that the advantages inherent in the present invention may not be impaired.

One of the modification comprises use of another component other than Sub-omponents (i) to (iii) during the process for preparing Component (A), such as methylhydrogenpolysiloxane, ethyl borate, aluminum triisopropoxide, aluminum trichloride, silicon tetrachloride, a tetra-valent titanium compound of a formula; Ti(OR⁹)₄__sX_s where R⁹ is a hydrocarbyl group preferably of 1 to 6 carbon atoms, X is a halogen atom, and s is 0 &lt; s &lt; 4, a tri-valent titanium compound, wolfram hexachloride, molybdenum pentachloride and the like.

The contact product of the Sub-components (i) to (iii) is washed amply with an inert hydrocarbon solvent to form the Component (A). Particular examples of the inert hydrocarbon solvent include those conventionally used in preparing the transition metal components for Ziegler catalysts such as, for example, hexane, heptane, octane, decane, cyclohexane and toluene.

One typical example of the optional component for modifying the Component (A) is a group of vinylsilane compounds.

Examples of vinylsilane compounds are derivatives of monosilane (SiH₄) such that at least one of the hydrogen atoms has been replaced by vinyl group (CH₂=CH-) and one or some of the remaining hydrogen atoms has been replaced by a halogen atom, preferably a chlorine atom, an alkyl, preferably one having 1 to 12 carbon atoms, an alkoxy, preferably one having 1 to 12 carbon atoms, or an aryl, preferably phenyl.

Specific examples of vinylsilane compounds include: CH₂-CH-SiH₃,

CH₂»CH-SiH₂(CH₃),

CH₂=CH-SiH(CH₃)₂,

CH₂=CH-Si(CH₃)₃,

CH₂«CH-SiCl₃,

CH₂=CH-SiCl₂(CH₃) ,

CH₂=CH-SiCl(CH₃)H,

CH₂=CH-SiCl ( C₂H₅) 2,

CH₂=CH-Si(C₂H₅)₃,

CH₂=CH-Si(CH₃) (C₂H₅)₂,

CH₂=CH-Si(C₆H₅)(CH₃)₂,

CH₂=CH-Si( CH₃ )₂(C₆H₄CH₃),

CH₂=CH-Si(OCH₃)₃,

CH₂=CH-Si (0C₂H₅ ) ₃,

CH₂=CH-Si(C₂H₅)(OCH₃)2,

CH₂=CH-Si(OC₂H₅)₂H,

CH,x CH,=CH CH \ I I

CH,-&gt; Si-0 -t Si-0 -n Si-CH, / I I ³

CH₃^z h CH (t = 10 - 20), ch₂=ch ch₃

CH₂=CH( CH₃ ) ₂-Si-O-Si ( CH₃ ) ₂ ( CH=CH₂ ), (CH₂=CH)₂SiCl₂, and (CH₂=CH)₂Si(CH₃)₂.

Preferable vinylsilane compounds are those having no oxygen atoms, and more preferable vinylsilane compounds are vinylalkylsilanes and vinylchlorosilanes.

The amount of the vinylsilane compounds is 0.001 to 1000, preferably 0.01 to 100, in terms of mole ratio to the titanium component of the component (i).

Component (B)

The component (B) is an organoaluminum compound represented by a formula ^R33-pV¹ wherein R³ indicates a hydrocarbyl group of up to 5 carbon atoms, preferably up to 4 carbon atoms, and p is a number satisfying an equation 0 ί pi 1. Examples of the organoaluminum compounds for

Component (B) includes Al(C₂H₅)₃, A1(CH₃)₃, Al(iC₃H₇)₃,

Al(n-C₃H₇)₃, A1(C₂H₅)₂H, Al{nC₃H₇)H, Al(iC₄H_g)₃,

Al(n-C₄H_g)₃, and Al(iC₄H_g)₂H. These can be used in admixture.

Making up of a catalyst

The catalysts in accordance with the present invention may be made up by contacting Components (A) and (B) or (A), (B) and an optional component each other at once, or step-wisely or portion-wisely, within or outside

<img file="CA2061963C_D0008.tif" />

a polymerization vessel in the absence or presence of an «-olefin to be polymerized.

The amount of the Component (B) used is, in accordance with one of the features of the present invention, no higher than 1, more preferably less than 1, but not less than 0.001, still preferably 0.001 to 1, more preferably 0.01 to 0.5, in terms of mole ratio of Al/Ti of the Component (B)/Component (A).

The Components (A) and (B) can be introduced to the place where they are contacted in any suitable way, but it may be preferred to bring it into contact each in a dispersion in an aliphatic hydrocarbon such as hexane or heptane before or after they are introduced into a polymerization vessel.

[II] Polymerization of olefins

The polymerization of olefins in accordance with the present invention is characterized by, inter alia, the temperature used, which is 150°C or higher.

The upper limit of the polymerization temperature may be around 300^eC. The preferable temperature range may be 150 to 250°C.

Not only are the catalysts of the present invention applicable to ordinary slurry polymerization but they may also be used for liquid-phase, solventless polymerization wherein substantially no solvent is used/ solution polymerization and vapor-phase polymerization, in a continuous or a batch-wise fashion. The catalysts in accordance with the present invention can be used not only in continuous polymerization and batchwise polymerization but also in the polymerization wherein a preliminary polymerization is conducted in which a small amount of an «-olefin is polymerized by the catalyst. In the case of slurry polymerization, aliphatic or aromatic hydrocarbons such as hexane, heptane, pentane, cyclohexane, benzene, toluene and kerosene are used alone or in combination as the polymerization solvent. The polymerization may be practiced under any pressure,

<img file="CA2061963C_D0009.tif" />

preferably under a pressure of atmospheric to 1000 kg/cm²G, preferably atmospheric to 150 kg/cm², and hydrogen can be used additionally as the molecular-weight control agent.

The olefins to be polymerized with the catalyst systems of the present invention are represented by the general formula:

r10-CH=CH₂ wherein R^1D is a hydrocarbyl group which has 1 to 10, preferably 1 to 6, carbon atoms and may be in a linear or branch structure.

Specific examples of such olefins may include propylene, butene-1, pentene-1, hexene-1, 3-methylbutene1 and 4-methylpentene-l. Preference is given to propylene, 3-methylbutene-l and 4-methylpentene-l, propylene being more preferable. These «-olefin can be used in combination.

The poly «-olefins thereby obtained are characterized by their molecular weight distribution which is broader than that in poly «-olefins produced at a temperature of 80°C or lower.

[EXPERIMENTAL EXAMPLES]

Example-1

[Preparation of Component (A))

Into a flask purged with nitrogen was introduced 200 ml of dehydrated and deoxygenated n-heptane, and subsequently 0.4 mol of MgCl₂ and 0.8 mol of Ti(O-nC₄H_g)₄and the reaction was carried out at 95°C for 2 hours. After completion of the reaction, the temperature was lowered to 40°C, followed by addition of 48 ml of methylhydrogenpolysiloxane (of 20 centistokes) and the reaction was carried out- for 3 hours. The solid component formed was washed with n-heptane.

Into a flask purged with nitrogen was introduced 50 ml of n-heptane purified similarly as described above, and the solid component synthesized above was introduced in an amount of 0.24 mol as calculated on Mg atom. Then, a mixture of 25 ml of n-heptane with 0.8 mol of SiCl₄ was introduced into the flask at 30°C over 30 minutes, and the reaction was carried out at 90°C for 4 hours. After completion of the reaction, the product was washed with n-heptane.

Into a flask purged with nitrogen was introduced 50 ml of amply purified n-heptane, and then 5 g of the solid component obtained above, Sub-component (i), was introduced. Next, 2.4 ml of (CH₃)₃CSi (CH₃) (OCH₃)₂ as the silicon compound of the Sub-component (ii), 2.0 ml of vinyltrimethylsilane as an optional component, and 3.0 g of triethylaluminum of the Sub-component (iii) were respectively introduced and contacted at 30°C for 2 hours.

The solid product obtained was thoroughly washed with n-heptane to provide the Component (A), which was found upon analysis on its portion to contain 2.50% by weight of titanium. The content of (CH₃)₃CSi(CH₃)(OCH₃)₂was 17.6% by weight.

[Polymerization of propylene)

Into a stainless steel autoclave with a stirring and a temperature control means of 1.5 liter capacity were introduced 500 ml of amply dehydrated and deoxygenated nparaffin, 3.0 mg of triethylaluminum as Component (B) and 100 mg of the above synthesized Component (A), the Al/Ti mole ratio being 0.5. Polymerization of propylene was conducted at a temperature of 170°C and under a pressure of 9 Kg/cm²G for 2 hours, after which the polymer solution obtained was subjected to treatment with methanol to separate the polymer from the n-paraffin and the polymer obtained was dried.

A polymer in a yield of 37.4 g was obtained.

The polymer had a content of the fraction soluble in xylene at 20°C, which is hereinbelow referred to as CXS, was 1.76% by weight.

The polymer had a molecular weight distribution such that the Q-value, which is a ratio of Mw/Mh where Mw stands for weight average molecular weight and M_N stands for number average molecular weight, upon the gel permeation chromatography was 7.1.

Example-2

[Preparation of Component (A))

Into a flask purged with nitrogen was introduced 200 ml of dehydrated and deoxygenated n-heptane, and subsequently 0.4 mol of MgCl₂ and 0.8 mol of Ti(O-nC₄H_g)₄and the reaction was carried at 95°C for 2 hours. After completion of the reaction, the temperature was lowered to 40°C, followed by addition of 48 ml of methylhydrogenpolysiloxane (of 20 centistokes) and the reaction was carried out for 3 hours. The solid component formed was washed with n-heptane.

Into a flask purged with nitrogen was introduced 50 ml of n-heptane purified similarly as described above, and the solid component synthesized above was introduced in an amount of 0.24 mol as calculated on Mg atom. Then, a mixture of 25 ml of n-heptane with 0.4 mol of SiCl₄ was introduced into the flask at 30^eC over 30 minutes, and the reaction was carried out at 70°C for 3 hours. After completion of the reaction, the product was washed with n-heptane.

Then, 0.024 mole of phthaloyl chloride in 25 ml of n-heptane was introduced into the flask at 90°C for 30 minutes and the reaction was conducted at 90°C for 1 hour. The product was then washed with n-heptane. 20 ml of SiCl₄ was then introduced and reacted at 80°C for 6 hours, after which the product was washed with n-heptane. The solid product produced was found to contain 1.21% by weight of titanium.

Into a flask purged with nitrogen was introduced 50 ml of thoroughly purified n-heptane, and then 5 g of the solid component obtained above, Sub-component (i), was introduced. Next, 1.2 ml of (CH₃)₃CSi (CH₃) (OCH₃)₂ as the silicon compound of the Sub-component (ii), 1.2 ml of divinyldimethylsilane as an optional component and 1.7 g of triethylaluminum of the Sub-component (iii) were respectively introduced and contacted at 30°C for 2 hours. After completion of the contact, the product was amply washed with n-heptane to provide a component (A), which was found to contain 0.89% by weight of titanium. The content of (CH₃)₃CSi(CH₃) (OCH₃)₂ was 9.6% by weight.

[Polymerization of propylene]

Polymerization of propylene was conducted as in Example-1 except for the use of 2.1 mg of triethylaluminum as Component (B). The polymer obtained was in an amount of 61.4 g and had the CXS of 1.01% by weight, the MPR of 45.3 g/10 rain, and the Q-value upon GPC analysis of 7.0.

Examples 3 to 6

Polymerization of propylene was conducted in which Component (A) prepared in Example-2 was used and under the conditions which are set forth in Table-1.

The results obtained are set forth in Table-1.

Table-:

<td colspan="2"> Q-value (Mw/Mh)</td><td> r»</td><td> 6.5</td><td> CM</td><td> n KO</td>

<td colspan="2"> -P ω ^ÿ tffi</td><td> o CM « rd</td><td> co σ\ o</td><td> KO H H</td><td> CO ro rH</td>

<td colspan="2"> Polymer yield (g)</td><td> CM • in in</td><td> 00 « σι σ&gt;</td><td> CM « Γ0 o·</td><td> 4 rd CM</td>

<td colspan="2">^H2 introduced (vol %)</td><td> o</td><td> ο Η</td><td> o</td><td> O</td>

<td rowspan="2"> Component (B) and amount used</td><td> Al/Ti (mole)</td><td> o • rd</td><td> m • ο</td><td> r* • o</td><td> r—1 O</td>

<td></td><td> rH CO en » *0· U</td><td> r-} &lt; &lt;*ϊ m m CM U</td><td> 3 o œ n * u •H</td><td> r~i 4 r&gt; in W (M U</td>

<td colspan="2"> Polymeri- zation temp. (°C)</td><td> O r- r-f</td><td> O KO rH</td><td> O in rH</td><td> O o ΓΜ</td>

<td colspan="2"> Example No.</td><td> CO</td><td></td><td> tn</td><td> KO</td>

Example 7

[Preparation of Component (A)]

Thirty (30) stainless steel balls of 12 mm diameter were loaded into a 0.47-liter ball mill, in which 20 g of anhydrous MgCl₂ and 2.2 ml of dibutyl phthalate were introduced for a 48-hour ball milling. Upon completion of this ball milling, 15 g of the milled composition was introduced into a flask which had been purged with nitrogen, and 50 ml of TiCl₄ was added to the flask wherein contact took place at 100°C for 2 hours. After completion of the contact, the contact product was thoroughly washed with n-heptane to give Sub-component (i)·

Next, 50 ml of thoroughly purified n-heptane were introduced into a flask which had been purged with nitrogen. Subsequently, 5 g of the Sub-component (i) obtained as above, 2.4 ml of

<img file="CA2061963C_D0010.tif" />

as Sub-component

Si(OCH₃)₃ (ii), 0.3 ml of TiCl₄, 1.5 g of A1(C₂H₅)₃ and 0.5 g of A1(C₂H₅)C1 as Sub-component (iii) were introduced thereinto for a 2-hour contact at 20°C. After the completion of this contact, the product was thoroughly washed with n-heptane to obtain the component (A), which was formed to contain 2.8% by weight of titanium and 9.2% by weight of the silicon compound as Sub-component (ii), namely

<img file="CA2061963C_D0011.tif" />

[Polymerization of propylene]

Polymerization of propylene was conducted as in Example-1 except for the use of 3.3 mg of (C₂H₅)₃A1 as the Component (B), Al/Ti mole ratio being 0.5.

The polymer obtained was in an amount of 41.7 g and had the CXS of 1.96% by weight and the Q-value of 7.7. Example 8

[Preparation of Component (A)]

Into a flask purged with nitrogen of a 500 ml capacity was introduced 10 g of Mg(OC₂H₅)₂, 100 ml of nheptane, and subsequently 30 ml of TiCl₄ and, after the temperature was raised to 70°C, 3.8 ml of di-n-octyl phthalate, and the temperature was then raised to 100°C and the contact was continued for 3 hours. The product of the contact was thoroughly washed with n-heptane to give sub-component (i).

Into a flask purged with nitrogen were introduced 50 ml of thoroughly purified n-heptane, 5 g of the sub-

<td> component</td><td> &lt;i) r</td><td> 1.8</td><td> ml</td><td> of</td><td> (iC₃H₇)₂Si(°CH₃)₂</td><td> as</td><td> sub-</td>

<td> component</td><td> (ü) i</td><td> 0.5</td><td> ml</td><td> of</td><td colspan="2"> vinyltrichlorosilane</td><td> as an</td>

<td> optional</td><td colspan="2"> component</td><td> and</td><td> 2.1</td><td> g of Al{C₂H₅)₃</td><td> as</td><td> sub-</td>

<td> component</td><td> (üi) f</td><td colspan="2"> followed</td><td> by</td><td> contact with each</td><td colspan="2"> other at</td>

<td> 30°C for</td><td colspan="2"> 2 hours.</td><td colspan="2"> The</td><td> contact product</td><td> was</td><td> then</td>

thoroughly washed with n-heptane to give Component (A), which was found to contain 1.9% by weight of titanium and 10.6% by weight of the silicon compound as the subcomponent (ii).

[Polymerization of propylene]

Polymerization of propylene was conducted as in Example-1 except for the use of 1.4 mg of A1(C₂H₅)₃, the mole ratio of Al/Ti being 0,..3, and for the temperature of 180°C.

The polymer obtained was in an amount of 54.4 g and had CXS of 1.58% by weight and Q of 7.7.

Example 9

[Preparation of Component (A)]

20S1963

Into a flask of 1 liter capacity purged with thoroughly purified nitrogen war; introduced 15 g of filings of metalic magnesium followed by thorough drying, 315 ml of di-n-butylether and, then, 78 ml of n-butyl chloride were introduced and contacted with each other at 50°C for 3 hours to form a solution of n-butylmagnesium chloride in di-n-butyl ether, to which 69 ml of SiCl₄ was added drop-wise at 15°C for 2 hours, followed by contact with each other at 20°C for 2 hours. After the contact, the solid product formed was washed with n-heptane. 5 g of the solid product thus obtained was sampled, to which 2.6 ml of cellosolve acetate was added, followed by contact with each other at 80°C for 2 hours. After the contact, the solid product was thoroughly washed with nheptane. To the solid product was added 50 ml of TiCl₄, followed by contact with each other at I00°C for 4 hours. After the contact, the solid product was thoroughly washed with n-heptane to give sub-component (i),

Into a flask purged with nitrogen was introduced 50 ml of thoroughly purified n-heptane, and the subcomponent (i) obtained above was introduced. Next, 0.25 ml of TiCl₄, 2.5 ml of ( silicon compound of sub-component (ii) and 3 g of triethylzinc as sub-component (iii) were respectively introduced and contacted at 40°C for 3 hours. The solid product obtained was thoroughly washed with n-heptane to provide the Component (A), which was found to contain 2.7% by weight of titanium and 8.3% by weight of the silicon compound as sub-component (ii).

[Polymerization of propylene]

Polymerization of propylene was conducted as in Example 1 except for the use of 0.48 mg of A1(C₂H₅)₃, the mole ratio of Al/Ti being 0.075 and for the temperature of 220°C,

The polymer was obtained in an amount of 11.4 g and had CXS of 1.62% by weight and Q of 7.1.

<img file="CA2061963C_D0012.tif" />

)(CH₃)Si(OCH₃)₂ as the

Comparative Example 1

Polymerization of propylene was conducted as in Example 1 except for the use of 3,000 mg of Al(C₂H₅)₃ of Component (B), the mole ratio of Al/Ti being 50. The polymer was obtained in an amount of only 1.2 g.