CN114507303A

CN114507303A - External electron donor for olefin polymerization, catalyst system and olefin polymerization method

Info

Publication number: CN114507303A
Application number: CN202011172025.1A
Authority: CN
Inventors: 周奇龙; 张锐; 徐秀东; 宋维玮; 尹珊珊; 于金华; 李凤奎
Original assignee: Sinopec Beijing Research Institute of Chemical Industry; China Petroleum and Chemical Corp
Current assignee: Sinopec Beijing Research Institute of Chemical Industry; China Petroleum and Chemical Corp
Priority date: 2020-10-28
Filing date: 2020-10-28
Publication date: 2022-05-17
Anticipated expiration: 2040-10-28
Also published as: CN114507303B

Abstract

The invention discloses an external electron donor for olefin polymerization, which comprises an amino ester compound shown in a formula (I) and a siloxane compound shown in a formula (II). The invention also discloses a catalyst system for olefin polymerization, which comprises the external electron donor; a solid catalyst component B containing magnesium, titanium, halogen and an internal electron donor compound; and an alkylaluminum compound C as a cocatalyst. When the catalyst system is used for propylene polymerization, the polymerization activity is high, the hydrogen regulation sensitivity is good, the stereospecificity is high, and meanwhile, the catalyst system has the performance of high-temperature self-inactivation.

R₁”_m”R₂”_n”Si(OR_3”)_{4‑m”‑n”}(II)。

Description

External electron donor for olefin polymerization, catalyst system and olefin polymerization method

Technical Field

The invention relates to an external electron donor for olefin polymerization, a catalyst system and an olefin polymerization method.

Background

The electron-donor compound being for CH₂One of the essential components of the Ziegler-Natta catalyst component of CHR olefin polymerization. Typically, the Ziegler-Natta catalyst system comprises the following three components: a solid titanium catalyst component having magnesium, titanium, halogen and an internal electron donor as essential components; an alkyl aluminum compound used as a cocatalyst; and an external electron donor compound for further improving the stereospecificity of the catalyst. The external electron donor compound and the internal electron donor are combined for use, so that the purpose of improving the performance of the catalyst can be achieved.

The olefin polymerization process is accompanied by an exotherm. Localized heat removal is not timely, resulting in a temperature increase. If the polymerization rate is maintained at a high rate with increasing temperature, local overheating is exacerbated, leading to plasticization and agglomeration of the polymer, thereby increasing the risk of stable operation of the apparatus. This phenomenon occurs in commercial gas phase polypropylene process units. If the activity of the Ziegler-Natta catalyst used drops sharply with increasing temperature, i.e.the catalyst has the characteristic of self-deactivation at high temperatures, this risk is advantageously reduced. Therefore, it is highly desirable to develop a Ziegler-Natta catalyst system that is active, orientable, etc. and has the characteristics of high temperature self-deactivation.

Disclosure of Invention

Aiming at the defects in the prior art, the invention aims to provide an external Electron Donor (ED) containing an amino ester compound and a siloxane compound and a corresponding Ziegler-Natta catalyst system, wherein the catalyst system has the characteristics of higher activity, good stereospecificity, good hydrogen regulation sensitivity and high-temperature self-inactivation when used for olefin polymerization.

The invention provides an external electron donor for olefin polymerization, which comprises an amino ester compound shown as a formula (I) and a siloxane compound shown as a formula (II),

wherein R is₁Selected from the group consisting of linear alkanes of 1 to 20 carbon atoms, branched alkyl of 3 to 20 carbon atoms, cycloalkyl of 3 to 20 carbon atoms, aryl of 6 to 20 carbon atoms, alkylaryl of 7 to 20 carbon atoms or arylalkyl of 7 to 20 carbon atoms, wherein the hydrogen atoms of the carbon in the alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl groups are optionally substituted or unsubstituted by heteroatoms, alkyl or alkoxy groups, and the carbon atoms of the alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl backbone are optionally substituted or unsubstituted by heteroatoms;

R₂and R₃(ii) are the same or different, each independently selected from a linear alkyl group of 1 to 20 carbon atoms, a branched alkyl group of 3 to 20 carbon atoms, a cycloalkyl group of 3 to 20 carbon atoms, an aryl group of 6 to 20 carbon atoms, an alkaryl group of 7 to 20 carbon atoms, or an aralkyl group of 7 to 20 carbon atoms, wherein a hydrogen atom in a carbon of the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl group is optionally substituted or unsubstituted with a heteroatom, an alkyl group, or an alkoxy group, and a carbon atom in the backbone of the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl group is optionally substituted or unsubstituted with a heteroatom; and R is₂And R₃Optionally connected to form a ring or not;

R₄and R₅Identical or different, each independently selected from the group consisting of linear alkanes of 1 to 20 carbon atoms, branched alkyl of 3 to 20 carbon atoms, cycloalkyl of 3 to 20 carbon atoms, aryl of 6 to 20 carbon atoms, alkylaryl of 7 to 20 carbon atoms or arylalkyl of 7 to 20 carbon atoms, the hydrogen atoms of the carbon atoms of said alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl groups being optionally substituted or unsubstituted by heteroatoms, alkyl or alkoxy groups, the said alkyl groups beingCarbon atoms of the radical, cycloalkyl, aryl, alkaryl or aralkyl backbone are optionally substituted or unsubstituted with heteroatoms;

R₁″_m″R₂″_n″Si(OR_3″)_4-m″-n″ (II)

in the formula (II), R₁"and R₂"identical or different, each independently selected from halogen, hydrogen atom, straight-chain alkyl of 1 to 20 carbon atoms, branched-chain alkyl of 3 to 20 carbon atoms, cycloalkyl of 3 to 20 carbon atoms, aryl of 6 to 20 carbon atoms or haloalkyl of 1 to 20 carbon atoms; r3' is selected from straight chain alkyl of 1-20 carbon atoms, branched alkyl of 3-20 carbon atoms, cycloalkyl of 3-20 carbon atoms, aryl of 6-20 carbon atoms or halogenated alkyl of 1-20 carbon atoms; m 'and n' are each independently selected from integers of 0-3, and m '+ n'<4。

According to the present invention, the phrase "optionally substituted with a heteroatom" means that it may or may not be substituted with a heteroatom. The hetero atom includes a halogen atom and the like. According to the invention, when bonded to form a ring, the resulting ring may or may not contain double bonds or heteroatoms in the backbone.

According to some embodiments of the invention, in formula (I), R₁Selected from a straight chain alkyl group of 1 to 10 carbon atoms, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms, an aryl group of 6 to 10 carbon atoms, an alkaryl group of 7 to 10 carbon atoms or an aralkyl group of 7 to 10 carbon atoms.

According to some embodiments of the invention, R₂And R₃Independently selected from a linear alkyl group of 3 to 10 carbon atoms, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms or an aryl group of 6 to 20 carbon atoms, preferably R₂And R₃Independently selected from a straight chain alkyl group of 1 to 6 carbon atoms or a branched alkyl group of 3 to 6 carbon atoms.

According to some embodiments of the invention, R₄And R₅Independently selected from a straight chain alkyl group of 1 to 10 carbon atoms, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms or 6 to 10 carbon atomsPreferably, R₄And R₅Is independently selected from a straight chain alkyl group of 1 to 6 carbon atoms or a branched alkyl group of 3 to 6 carbon atoms, further preferably R₄And R₅Independently selected from hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl or phenyl.

According to some embodiments of the invention, the heteroatom comprises a halogen atom.

According to some embodiments of the invention, when R₂And R₃When linked to form a ring, the resulting ring may or may not contain double bonds or heteroatoms in the backbone.

According to some embodiments of the invention, in formula (II), R₁"and R₂"are each independently selected from the group consisting of halogen, hydrogen, straight chain alkyl of 1 to 10 carbon atoms, branched alkyl of 3 to 10 carbon atoms, cycloalkyl of 3 to 10 carbon atoms, aryl of 6 to 10 carbon atoms, or haloalkyl of 1 to 10 carbon atoms; r3' is selected from straight chain alkyl of 1-10 carbon atoms, branched alkyl of 3-10 carbon atoms, cycloalkyl of 3-10 carbon atoms, aryl of 6-10 carbon atoms or halogenated alkyl of 1-10 carbon atoms.

According to some embodiments of the invention, the amino ester compound is selected from at least one of the following compounds: ethyl N, N-dipropylaminoacetate, propyl N, N-dipropylaminoacetate, butyl N, N-dipropylaminoacetate, isobutyl N, N-dipropylaminoacetate, 1-pentanol N, N-dipropylaminoacetate, 1-hexanol N, N-dipropylaminoacetate, 1-heptanol N, N-dipropylaminoacetate, 1-octanol N, N-dipropylaminoacetate, 1-nonanol N, N-dipropylaminoacetate, 1-decanol N, N-dipropylaminoacetate, phenol N, N-dipropylaminoacetate, o-methylphenol N, N-dipropylaminoacetate, butyl N, N-diallylaminoacetate, ethyl N, N-dibutylaminoacetate, butyl N, N-dipropylaminoacetate, butyl N-dipropylaminoacetate, N-1-heptanol N, N-dipropylaminoacetate, N-1-octanol N, N-dipropylaminoacetate, N-1-octanol, N-dipropylaminoacetate, butyl acetate, N-dipropylaminoacetate, N-isopropylacetate, N-1-isopropylamide, N-isopropylamino-acetate, N-isopropylamino-N-isopropylamino-and a, Propyl N, N-dibutylaminoacetate, butyl N, N-dibutylaminoacetate, isobutyl N, N-dibutylaminoacetate, 1-pentanol N, N-dibutylaminoacetate, 1-hexanol N, N-dibutylaminoacetate, 1-heptanol N, N-dibutylaminoacetate, 1-octanol N, N-dibutylaminoacetate, 1-nonanol N, N-dibutylaminoacetate, 1-decanol N, N-dibutylaminoacetate, phenol N, N-dibutylaminoacetate, o-methylphenol N, N-dibutylaminoacetate, ethyl N, N-dipentylaminoacetate, propyl N, N-dipentylaminoacetate, butyl N, N-dipentylaminoacetate, Isobutyl N, N-dipentylaminoacetate, 1-amyl N, N-dipentylaminoacetate, 1-hexyl N, N-dipentylaminoacetate, 1-heptyl N, N-dipentylaminoacetate, 1-octyl N, N-dipentylaminoacetate, 1-nonyl N, N-dipentylaminoacetate, 1-decyl N, N-dipentylaminoacetate, phenol N, N-dipentylaminoacetate, o-methylphenol N, N-dipentylaminoacetate, ethyl N, N-dihexylaminoacetate, propyl N, N-dihexylaminoacetate, butyl N, N-dihexylaminoacetate, isobutyl N, N-dihexylaminoacetate, 1-amyl N, N-dihexylaminoacetate, 1-hexanol N, N-dihexylaminoacetate, 1-heptanol N, N-dihexylaminoacetate, 1-octanol N, N-dihexylaminoacetate, 1-nonanol N, N-dihexylaminoacetate, 1-decanol N, N-dihexylaminoacetate, phenol N, N-dihexylaminoacetate, o-methylphenol N, N-dihexylaminoacetate, ethyl N, N-dihexylaminoacetate, propyl N, N-dihexylaminoacetate, butyl N, N-dihexylaminoacetate, isobutyl N-dihexylaminoacetate, 1-pentanol N, N-dihexylaminoacetate, 1-hexanol N, N-dihexylaminoacetate, N, N-1-heptylaminoacetic acid-1-heptanol ester, N-1-octanylglycine-1-octanol ester, N-1-nonane-, N-1-decanol-, phenol-, o-methylphenol-, ethyl-, propyl-, butyl-, isobutyl-, 1-pentanol-, N-dioctylaminoacetic acid-1-pentanol ester, N-1-hexanol-, 1-heptanol-, N-dioctylaminoacetic acid-1-heptanol ester, 1-octyl N, N-dioctylaminoacetate, 1-nonyl N, N-dioctylaminoacetate, 1-decyl N, N-dioctylaminoacetate, phenol N, N-dioctylaminoacetate, o-methylphenol N, N-dioctylaminoacetate, ethyl N, N-di-isooctylaminoacetate, propyl N, N-di-isooctylaminoacetate, butyl N, N-di-isooctylaminoacetate, isobutyl N, N-di-isooctylaminoacetate, 1-pentyl N, N-di-isooctylaminoacetate, 1-hexyl N, N-di-isooctylaminoacetate, 1-heptyl N, N-di-isooctylaminoacetate, 1-octyl alcohol N, N-di-isooctylaminoacetate, 1-nonyl N, N-diisooctylaminoacetate, 1-decyl N, N-diisooctylaminoacetate, phenol N, N-diisooctylaminoacetate, o-cresol N, N-diisooctylaminoacetate, ethyl N, N-dinonylaminoacetate, propyl N, N-dinonylaminoacetate, butyl N, N-dinonylaminoacetate, isobutyl N, N-dinonylaminoacetate, 1-amyl N, N-dinonylaminoacetate, 1-hexyl N, N-dinonylaminoacetate, 1-heptyl N, N-dinonylaminoacetate, 1-octyl N, N-dinonylaminoacetate, 1-nonyl N, N-dinonylaminoacetate, 1-decyl N, N-dinonylaminoacetic acid, phenol N, N-dinonylaminoacetic acid, o-methyl phenol N, N-dinonylaminoacetic acid, ethyl N, N-didecylaminoacetic acid, propyl N, N-didecylaminoacetic acid, butyl N, N-didecylaminoacetic acid, isobutyl N, N-didecylaminoacetic acid, 1-pentyl N, N-didecylaminoacetic acid, 1-hexyl N, N-didecylaminoacetic acid, 1-heptyl N, N-didecylaminoacetic acid, 1-octyl N, N-didecylaminoacetic acid, 1-nonyl N, N-didecylaminoacetic acid, 1-decyl N, N-didecylaminoacetic acid, Phenol N, N-didecyl amino acetate and o-methyl phenol N, N-didecyl amino acetate.

According to some embodiments of the invention, the siloxane compound is selected from the group consisting of trimethylmethoxysilane, diisopropyldimethoxysilane, diisobutyldimethoxysilane, isopropylisobutyldimethoxysilane, di-t-butyldimethoxysilane, t-butylmethyldimethoxysilane, t-butylethyldimethoxysilane, t-butylpropyldimethoxysilane, t-butylisopropyldimethoxysilane, cyclohexylmethyldimethoxysilane, dicyclohexyldimethoxysilane, cyclohexyl-t-butyldimethoxysilane, cyclopentylmethyl-dimethoxysilane, cyclopentylethyldimethoxysilane, dicyclopentyldimethoxysilane, cyclopentylcyclohexyldimethoxysilane, bis (2-methylcyclopentyl) dimethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, phenyltriethoxysilane, di-t-butyldimethoxysilane, t-butylmethyldimethoxysilane, di-t-butyldimethoxysilane, di-t-butylmethyldimethoxysilane, di-t-butyldimethoxysilane, cyclopentylethyldimethoxysilane, di-2-ethyldimethoxysilane, di-t-ethyldimethoxysilane, di-2-ethyldimethoxysilane, di-methyldiethoxysilane, di-ethyldimethoxysilane, di-N, At least one of methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, isopropyltrimethoxysilane, isopropyltriethoxysilane, butyltrimethoxysilane, butyltriethoxysilane, isobutyltrimethoxysilane, isobutyltriethoxysilane, pentyltrimethoxysilane, isopentyltrimethoxysilane, cyclopentyltrimethoxysilane, cyclohexyltrimethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, tetramethoxysilane, tetraethoxysilane, and tetrabutoxysilane.

According to some embodiments of the present invention, the amino ester compound accounts for 5-95 mol% of the external electron donor a, and may be, for example, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90% and any value therebetween.

According to a preferred embodiment of the present invention, the amino ester compound accounts for 5-60 mol% of the external electron donor A.

According to a further preferred embodiment of the present invention, the amino ester compound accounts for 10-40 mol% of the external electron donor a.

The present inventors have surprisingly found that the application of a Ziegler-Natta catalyst system comprising an amino ester compound and a siloxane compound as external electron donors to CH₂The CHR olefin has the characteristic of high-temperature self-inactivation during polymerization.

The high-temperature self-deactivation performance of the invention means that the activity of the catalyst is greatly reduced at a specific test temperature, but the activity is not reduced to an inactive state. In general, Ziegler-Natta catalysts exhibit some reduction in polymerization temperature above 90 ℃. The high-temperature self-deactivation means that when the polymerization temperature is increased from 70 ℃ to 100 ℃ in the conventional bulk polymerization, the polymerization activity of the catalyst is reduced to below 30% of the original activity regardless of the change of the bulk concentration of the monomer.

A second aspect of the present invention provides a catalyst system for the polymerization of olefins comprising

(1) An external electron donor A;

(2) a solid catalyst component B containing magnesium, titanium, halogen and an internal electron donor compound; and

(3) an alkylaluminum compound C as a cocatalyst;

wherein the external electron donor A comprises an amino ester compound shown as a formula (I),

in the formula (I), R₁Selected from the group consisting of linear alkanes of 1 to 20 carbon atoms, branched alkyl of 3 to 20 carbon atoms, cycloalkyl of 3 to 20 carbon atoms, aryl of 6 to 20 carbon atoms, alkylaryl of 7 to 20 carbon atoms or arylalkyl of 7 to 20 carbon atoms, wherein the hydrogen atoms of the carbon in the alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl groups are optionally substituted or unsubstituted by heteroatoms, alkyl or alkoxy groups, and the carbon atoms of the alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl backbone are optionally substituted or unsubstituted by heteroatoms;

R₄and R₅The same or different, each independently selected from the group consisting of a linear alkane of 1 to 20 carbon atoms, a branched alkyl of 3 to 20 carbon atoms, a cycloalkyl of 3 to 20 carbon atoms, an aryl of 6 to 20 carbon atoms, an alkaryl of 7 to 20 carbon atoms, or an aralkyl of 7 to 20 carbon atoms, wherein the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl groupThe hydrogen atoms on the carbon are optionally substituted or not substituted by heteroatoms, alkyl or alkoxy, the carbon atoms on the alkyl, cycloalkyl, aryl, alkaryl or aralkyl main chain are optionally substituted or not substituted by heteroatoms;

R₁″_m″R₂″_n″Si(OR_3″)_4-m″-n″ (II)

According to some embodiments of the invention, R₄And R₅Independently selected from linear alkanes of 1 to 10 carbon atomsA group, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms or an aryl group of 6 to 10 carbon atoms, preferably, R₄And R₅Independently selected from a straight chain alkyl group of 1 to 6 carbon atoms or a branched alkyl group of 3 to 6 carbon atoms, further preferably R₄And R₅Independently selected from hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl or phenyl.

According to some embodiments of the invention, the amino ester compound is selected from at least one of the following compounds: ethyl N, N-dipropylaminoacetate, propyl N, N-dipropylaminoacetate, butyl N, N-dipropylaminoacetate, isobutyl N, N-dipropylaminoacetate, 1-pentanol N, N-dipropylaminoacetate, 1-hexanol N, N-dipropylaminoacetate, 1-heptanol N, N-dipropylaminoacetate, 1-octanol N, N-dipropylaminoacetate, 1-nonanol N, N-dipropylaminoacetate, 1-decanol N, N-dipropylaminoacetate, phenol N, N-dipropylaminoacetate, o-methylphenol N, N-dipropylaminoacetate, butyl N, N-diallylaminoacetate, ethyl N, N-dibutylaminoacetate, butyl N, N-dipropylaminoacetate, butyl N-dipropylaminoacetate, N-1-heptanol N, N-dipropylaminoacetate, N-1-octanol N, N-dipropylaminoacetate, N-1-octanol, N-dipropylaminoacetate, butyl acetate, N-dipropylaminoacetate, N-isopropylacetate, N-1-isopropylamide, N-isopropylamino-acetate, N-isopropylamino-N-isopropylamino-and a, Propyl N, N-dibutylaminoacetate, butyl N, N-dibutylaminoacetate, isobutyl N, N-dibutylaminoacetate, 1-pentanol N, N-dibutylaminoacetate, 1-hexanol N, N-dibutylaminoacetate, 1-heptanol N, N-dibutylaminoacetate, 1-octanol N, N-dibutylaminoacetate, 1-nonanol N, N-dibutylaminoacetate, 1-decanol N, N-dibutylaminoacetate, phenol N, N-dibutylaminoacetate, o-methylphenol N, N-dibutylaminoacetate, ethyl N, N-dipentylaminoacetate, propyl N, N-dipentylaminoacetate, butyl N, N-dipentylaminoacetate, Isobutyl N, N-dipentylaminoacetate, 1-amyl N, N-dipentylaminoacetate, 1-hexyl N, N-dipentylaminoacetate, 1-heptyl N, N-dipentylaminoacetate, 1-octyl N, N-dipentylaminoacetate, 1-nonyl N, N-dipentylaminoacetate, 1-decyl N, N-dipentylaminoacetate, phenol N, N-dipentylaminoacetate, o-methylphenol N, N-dipentylaminoacetate, ethyl N, N-dihexylaminoacetate, propyl N, N-dihexylaminoacetate, butyl N, N-dihexylaminoacetate, isobutyl N, N-dihexylaminoacetate, 1-amyl N, N-dihexylaminoacetate, 1-hexanol N, N-dihexylaminoacetate, 1-heptanol N, N-dihexylaminoacetate, 1-octanol N, N-dihexylaminoacetate, 1-nonanol N, N-dihexylaminoacetate, 1-decanol N, N-dihexylaminoacetate, phenol N, N-dihexylaminoacetate, o-methylphenol N, N-dihexylaminoacetate, ethyl N, N-dihexylaminoacetate, propyl N, N-dihexylaminoacetate, butyl N, N-dihexylaminoacetate, isobutyl N-dihexylaminoacetate, 1-pentanol N, N-dihexylaminoacetate, 1-hexanol N, N-dihexylaminoacetate, N, N-1-heptylaminoacetic acid-1-heptanol ester, N-1-octanylglycine-1-octanol ester, N-1-nonane-, N-1-decanol-, phenol-, o-methylphenol-, ethyl-, propyl-, butyl-, isobutyl-, 1-pentanol-, N-dioctylaminoacetic acid-1-pentanol ester, N-1-hexanol-, 1-heptanol-, N-dioctylaminoacetic acid-1-heptanol ester, 1-octyl N, N-dioctylaminoacetate, 1-nonyl N, N-dioctylaminoacetate, 1-decyl N, N-dioctylaminoacetate, phenol N, N-dioctylaminoacetate, o-methylphenol N, N-dioctylaminoacetate, ethyl N, N-di-isooctylaminoacetate, propyl N, N-di-isooctylaminoacetate, butyl N, N-di-isooctylaminoacetate, isobutyl N, N-di-isooctylaminoacetate, 1-pentyl N, N-di-isooctylaminoacetate, 1-hexyl N, N-di-isooctylaminoacetate, 1-heptyl N, N-di-isooctylaminoacetate, 1-octyl alcohol N, N-di-isooctylaminoacetate, 1-nonyl N, N-diisooctylaminoacetate, 1-decyl N, N-diisooctylaminoacetate, phenol N, N-diisooctylaminoacetate, o-methylphenol N, N-diisooctylaminoacetate, ethyl N, N-dinonylaminoacetate, propyl N, N-dinonylaminoacetate, butyl N, N-dinonylaminoacetate, isobutyl N, N-dinonylaminoacetate, 1-pentylol N, N-dinonylaminoacetate, 1-hexylol N, N-dinonylaminoacetate, 1-heptol N, N-dinonylaminoacetate, 1-octylol N, N-dinonylaminoacetate, 1-nonylacetic acid ester, N-dinonylaminoacetic acid, 1-nonylacetic acid ester, N-dinonylaminoacetic acid, N-octylol, N-dinonylaminoacetic acid, 1-nonylacetic acid ester, N-dinonylamino, 1-decyl N, N-dinonylaminoacetic acid, phenol N, N-dinonylaminoacetic acid, o-methyl phenol N, N-dinonylaminoacetic acid, ethyl N, N-didecylaminoacetic acid, propyl N, N-didecylaminoacetic acid, butyl N, N-didecylaminoacetic acid, isobutyl N, N-didecylaminoacetic acid, 1-pentyl N, N-didecylaminoacetic acid, 1-hexyl N, N-didecylaminoacetic acid, 1-heptyl N, N-didecylaminoacetic acid, 1-octyl N, N-didecylaminoacetic acid, 1-nonyl N, N-didecylaminoacetic acid, 1-decyl N, N-didecylaminoacetic acid, Phenol N, N-didecyl amino acetate and o-methyl phenol N, N-didecyl amino acetate.

According to some embodiments of the invention, the siloxane is selected from the group consisting of trimethylmethoxysilane, diisopropyldimethoxysilane, diisobutyldimethoxysilane, isopropylisobutyldimethoxysilane, di-t-butyldimethoxysilane, t-butylmethyldimethoxysilane, t-butylethyldimethoxysilane, t-butylpropyldimethoxysilane, t-butylisopropyldimethoxysilane, cyclohexylmethyldimethoxysilane, dicyclohexyldimethoxysilane, cyclohexyl-t-butyldimethoxysilane, cyclopentylmethyl-dimethoxysilane, cyclopentylethyldimethoxysilane, dicyclopentyldimethoxysilane, cyclopentylcyclohexyldimethoxysilane, bis (2-methylcyclopentyl) dimethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, phenyltriethoxysilane, bis (2-methylcyclopentyl) dimethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, N-butyldimethoxysilane, N-bis (B-butyldimethoxysilane, N-butyltrimethoxysilane, N-butyldimethoxysilane, N-N, S, at least one of methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, isopropyltrimethoxysilane, isopropyltriethoxysilane, butyltrimethoxysilane, butyltriethoxysilane, isobutyltrimethoxysilane, isobutyltriethoxysilane, pentyltrimethoxysilane, isopentyltrimethoxysilane, cyclopentyltrimethoxysilane, cyclohexyltrimethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, tetramethoxysilane, tetraethoxysilane, and tetrabutoxysilane.

According to some embodiments of the present invention, the internal electron donor compound is selected from at least one of phthalate-based compounds, glycol-based compounds, cyanosuccinate-based compounds, diether-based compounds, and succinate-based compounds; preferably at least one selected from the group consisting of glycol ester compounds, cyanosuccinate compounds, diether compounds and succinate compounds; more preferably from the diether class

According to the preparation method of the catalyst solid component B, a magnesium compound, a titanium compound and an internal electron donor compound can be contacted and reacted under certain conditions. The amounts of the titanium compound, the magnesium compound and the internal electron donor used for preparing the solid component of the catalyst are not particularly limited and may be those conventionally used in the art, respectively.

According to some embodiments of the present invention, in the solid catalyst component B, the content of magnesium is 1.0 to 8.0 wt%, preferably 1.6 to 6.0 wt%, calculated as magnesium atoms, titanium is titanium atoms, calculated as halogen atoms, titanium atoms are 1.0 to 8.0 wt%; the content of magnesium atoms is preferably 10 to 70 wt%, preferably 15 to 40 wt%; the content of halogen atoms is 20 to 90 wt%, preferably 30 to 85 wt%; the content of the internal electron donor compound is 2-30 wt%, preferably 3-20 wt%.

In a preferred case, the magnesium compound may be at least one of a magnesium compound represented by formula (II), a hydrate of the magnesium compound represented by formula (II), and an alcohol adduct of the magnesium compound represented by formula (II),

MgR₁₁R₁₂ (II)

in the formula (II), R₁₁And R₁₂The same or different, each independently selected from the group consisting of halogen, linear alkoxy of 1 to 8 carbon atoms, branched alkoxy of 3 to 8 carbon atoms, linear alkyl of 1 to 8 carbon atoms, or branched alkyl of 3 to 8 carbon atoms.

According to the method for preparing the catalyst solid component B of the present invention, the hydrate of the magnesium compound represented by the formula (II) is MgR₁₁R₁₂·pH₂O, wherein p is in the range of 0.1 to 6, preferably 2 to 3.5. In the present invention, the alcohol adduct means MgR₁₁R₁₂·qR₁₃OH, wherein R₁₃Selected from the group consisting of hydrocarbyl of 1 to 18 carbon atoms, preferably alkyl of 1 to 8 carbon atoms, more preferably methyl, ethyl, n-propyl or isopropyl; q is in the range of 0.1 to 6, preferably 2 to 3.5.

In a preferred case, the magnesium compound may be at least one of dimethoxymagnesium, diethoxymagnesium, dipropoxymagnesium, diisopropoxymagnesium, dibutoxymagnesium, diisobutyoxymagnesium, dipentyoxymagnesium, dihexomagnesium, bis (2-ethyl) hexyloxymagnesium, methoxymagnesium chloride, methoxymagnesium bromide, methoxymagnesium iodide, ethoxymagnesium chloride, ethoxymagnesium bromide, ethoxymagnesium iodide, propoxymagnesium chloride, propoxymasium bromide, propoxymasium iodide, butoxymagnesium chloride, butoxymagnesium bromide, butoxymagnesium iodide, methylmagnesium chloride, ethylmagnesium chloride, propylmagnesium chloride, butylmagnesium chloride, pentylmagnesium chloride, phenylmagnesium chloride, magnesium dichloride, magnesium dibromide, magnesium diiodide, an alcohol adduct of magnesium dichloride, an alcohol adduct of magnesium dibromide, and an alcohol adduct of magnesium diiodide. Most preferably, the magnesium compound contains at least one of diethoxymagnesium, butylmagnesium chloride, ethoxymagnesium chloride, magnesium dichloride.

The process for the preparation of the solid component B of the catalyst according to the invention, wherein the titanium compound is a compound of formula (III),

TiX_m(OR₁₄)_4-m (III)

in the formula (III), X is halogen and R₁₄Selected from hydrocarbon groups of 1 to 20 carbon atoms, and m is an integer of 0 to 4. The halogen may be chlorine, bromine or iodine.

In a preferred aspect, in formula (III), X is halogen and R is₁₄Selected from alkyl groups of 1 to 5 carbon atoms, for example: titanium tetrachloride, titanium tetrabromide, titanium tetraiodide, tetrabutoxytitanium, tetraethoxytitanium, chlorotriethoxytitanium, dichlorodiethoxytitanium and trichloromonoethoxytitanium. Most preferably, the titanium compound is titanium tetrachloride.

In the present invention, the catalyst solid component B may be carried out by a method for preparing an olefin catalyst component which is conventional in the art. The solid catalyst component of the present invention can be prepared, for example, by the following method.

In the first method, alkoxy magnesium or alkoxy magnesium halide is suspended in an inert diluent to form a suspension, and the suspension is mixed with the titanium compound and the internal electron donor to contact to obtain a solid dispersion system, which is generally called mother liquor. Filtering the mother liquor, and suspending the obtained solid substance in a solution containing titanium tetrachloride for contact treatment, which is generally called titanium treatment; then filtering and washing to obtain the catalyst solid component of the invention.

Specific examples of the above-mentioned alkoxymagnesium include dimethoxymagnesium, diethoxymagnesium, dipropoxymagnesium, diisopropoxymagnesium, dibutoxymagnesium, diisobutyoxymagnesium, dipentyoxymagnesium, dihexyloxymagnesium, di (2-ethyl) hexyloxymagnesium, and the like, or a mixture thereof, and diethoxymagnesium or a mixture of diethoxymagnesium and other alkoxymagnesium is preferable. The preparation method of the alkoxy magnesium compound can be prepared by a method known in the art, such as the preparation method disclosed in patent CN101906017A by mixing metal magnesium with fatty alcohol in the presence of a small amount of iodine.

Specific examples of the alkoxymagnesium halide include methoxymagnesium chloride, ethoxymagnesium chloride, propoxymagnesium chloride, butoxymagnesium chloride, etc., and ethoxymagnesium chloride is preferable. The alkoxy magnesium halide compound can be prepared by a method known in the art, such as a method of mixing a Grignard reagent of butyl magnesium chloride with tetraethoxy titanium and tetraethoxy silicon to prepare ethoxy magnesium chloride.

The inert diluent used for forming the mother liquor in the first method can adopt at least one of hexane, heptane, octane, decane, benzene, toluene and xylene.

The amount of each component used for forming the mother liquor in the first process is 0.5 to 100 moles, preferably 1 to 50 moles, of the titanium compound per mole of magnesium; the inert diluent is used in an amount of usually 0.5 to 100 moles, preferably 1 to 50 moles; the total amount of the internal electron donor compound (ID) is usually 0.005 to 10 mol, preferably 0.01 to 1 mol.

The contact temperature of the components during the formation of the mother liquor in the first method is generally-40-200 ℃, preferably-20-150 ℃; the contact time is usually 1 minute to 20 hours, preferably 5 minutes to 8 hours.

In the titanium treatment in the first method, an inert diluent such as at least one of hexane, heptane, octane, decane, benzene, toluene and xylene may be optionally added to the titanium tetrachloride-containing solution used.

In the titanium treatment process in the first method, the titanium compound is used in an amount of 0.5 to 100 moles, preferably 1 to 50 moles, per mole of magnesium, based on the amount of each component in the titanium tetrachloride-containing solution; the inert diluent is used in an amount of usually 0 to 100 mol, preferably 0 to 50 mol.

The number of titanium treatments in the above method one is 0 to 10, preferably 1 to 5.

In the first method, the electron donor compound can be selectively added during the titanium treatment, wherein the amount of the internal electron donor is usually 0.005-10 mol, preferably 0.01-1 mol.

In the first method, the titanium treatment temperature is usually 0-200 ℃, and preferably 30-150 ℃; the contact time is usually 1 minute to 20 hours, preferably 5 minutes to 6 hours.

Dissolving magnesium dihalide in a solvent system consisting of an organic epoxy compound, an organic phosphorus compound, a fatty alcohol compound and an inert diluent to form a uniform solution, then contacting and reacting the uniform solution with the titanium compound and the electron donor compound, and separating out solids in the presence of a precipitation assistant to form a mother solution; filtering the mother liquor, and suspending the obtained solid substance in a solution containing titanium tetrachloride for contact treatment, which is generally called titanium treatment below; then filtering and washing to obtain the catalyst solid component of the invention.

The precipitation aid used in the second method is not particularly limited as long as it can precipitate and form solid particles. Examples which may be mentioned are: at least one of an organic acid anhydride, an organic acid, an ester, an ether, and a ketone. Specific examples of the organic acid anhydride may be at least one of acetic anhydride, phthalic anhydride, succinic anhydride, maleic anhydride, etc., specific examples of the organic acid may be at least one of acetic acid, propionic acid, butyric acid, acrylic acid, methacrylic acid, etc., specific examples of the ester may be at least one of dibutyl phthalate, 2, 4-pentanediol dibenzoate, 3-ethyl-2, 4-pentanediol dibenzoate, 2, 3-diisopropyl-1, 4-butanediol dibenzoate, 3, 5-heptanediol dibenzoate, and 4-ethyl-3, 5-heptanediol dibenzoate, and specific examples of the ether may be methyl ether, ethyl ether, propyl ether, butyl ether, pentyl ether, 2-isopropyl-2-isopentyl dimethoxy propane, and 9, at least one of 9- (dimethoxymethyl) fluorene, and the ketone can be at least one of acetone, methyl ethyl ketone and benzophenone.

The organic epoxy compound used in the second process may be at least one selected from the group consisting of ethylene oxide, propylene oxide, butylene oxide, butadiene double oxide, epichlorohydrin, methyl glycidyl ether, diglycidyl ether, and the like, and epichlorohydrin is preferable.

The organic phosphorus compound used in the second process may be a hydrocarbyl or halohydrocarbyl ester of orthophosphoric acid or phosphorous acid, and specific examples of the organic phosphorus compound include: trimethyl orthophosphate, triethyl orthophosphate, tributyl orthophosphate, triphenyl orthophosphate, trimethyl phosphite, triethyl phosphite, tributyl phosphite, benzyl phosphite, or the like, with tributyl orthophosphate being preferred.

The fatty alcohol compound used in the second method may be a straight-chain or branched-chain alkane having 1 to 20 carbon atoms, a monohydric or branched-chain fatty alcohol, preferably a straight-chain or branched-chain monohydric fatty alcohol having 1 to 10 carbon atoms, and specific examples thereof include: methanol, ethanol, propanol, isopropanol, butanol, isobutanol, pentanol, hexanol, heptanol, (2-ethyl) hexyl alcohol, octanol, nonanol, decanol, etc., with (2-ethyl) hexyl alcohol being preferred.

As the inert diluent used in the formation of the mother liquor in the second process, at least one of hexane, heptane, octane, decane, benzene, toluene and xylene can be used.

The amount of each component used in the formation of the mother liquor in the above-mentioned second process may be 0.2 to 10 moles, preferably 0.5 to 4 moles, of the organic epoxy compound per mole of the magnesium halide; the organic phosphorus compound may be present in an amount of 0.1 to 3 moles, preferably 0.3 to 1.5 moles; the fatty alcohol compound may be in the range of 0.2 to 10 moles, preferably 0.5 to 3 moles; the titanium compound may be in the range of 0.5 to 20 moles, preferably 5 to 15 moles; the precipitation-assisting component may be 0.01 to 0.3 mol, preferably 0.02 to 0.2 mol; the total amount of the internal electron donor compound (ID) may be 0 to 10 moles, preferably 0.02 to 0.3 moles.

The contact temperature of the components in the formation of the mother liquor in the second process is usually-40 to 200 ℃, preferably-20 to 150 ℃; the contact time is usually 1 minute to 20 hours, preferably 5 minutes to 8 hours.

In the titanium treatment described in the second method, an inert diluent such as at least one of hexane, heptane, octane, decane, benzene, toluene and xylene may be optionally added to the titanium tetrachloride-containing solution used.

In the titanium treatment in the second process, the titanium compound is used in an amount of 0.5 to 100 mol, preferably 1 to 50mol, per mol of magnesium as the components in the titanium tetrachloride-containing solution; the inert diluent is used in an amount of usually 0 to 100 mol, preferably 0 to 50 mol.

The number of titanium treatments in the above second method is 0 to 10 times, preferably 1 to 5 times.

In the second method, the electron donor compound can be optionally added during the titanium treatment, wherein the amount of the internal electron donor is usually 0.005 to 10 mol, preferably 0.01 to 1 mol.

In the second method, the titanium treatment temperature is usually 0 to 200 ℃, preferably 30 to 150 ℃; the contact time is usually 1 minute to 20 hours, preferably 5 minutes to 6 hours.

Suspending the alcohol adduct of magnesium dihalide in an inert diluent to form a suspension, and mixing and contacting the suspension with the titanium compound and the internal electron donor (ID) to obtain a solid dispersion system, which is hereinafter generally referred to as mother liquor. Filtering the mother liquor, and suspending the obtained solid substance in a solution containing titanium tetrachloride for contact treatment, which is generally called titanium treatment below; then filtering and washing to obtain the catalyst solid component of the invention.

The alcohol adduct of magnesium dihalide described in the above process three can be prepared by the following method: mixing alcohol (such as methanol, ethanol, propanol or isopropanol) and magnesium halide in the presence of inert solvent (such as hexane, heptane, octane, decane, benzene, toluene and xylene) which is not miscible with adduct to form emulsion, rapidly quenching and dispersing the emulsion, and obtaining spherical particles, namely the alcohol adduct of magnesium dihalide.

The inert diluent used for the formation of the mother liquor in the third method can adopt at least one of hexane, heptane, octane, decane, benzene, toluene and xylene.

The amount of each component used for forming the mother liquor in the third process is 0.5 to 100 moles, preferably 1 to 50 moles, of the titanium compound per mole of magnesium; the inert diluent is used in an amount of usually 0.5 to 100 moles, preferably 1 to 50 moles; the total amount of the electron donor compound (ID) is usually 0.005 to 10 mol, preferably 0.01 to 1 mol.

The contact temperature of the components during the formation of the mother liquor in the third method is generally-40-200 ℃, and preferably-20-150 ℃; the contact time is usually 1 minute to 20 hours, preferably 5 minutes to 8 hours.

In the titanium treatment process described in the third method, an inert diluent such as at least one of hexane, heptane, octane, decane, benzene, toluene and xylene may be optionally added to the titanium tetrachloride-containing solution used.

In the titanium treatment process in the third method, the used amount of each component in the titanium tetrachloride-containing solution is 0.5 to 100 mol, preferably 1 to 50mol, per mol of magnesium; the inert diluent is used in an amount of usually 0 to 100 moles, preferably 0 to 50 moles.

The number of titanium treatments in the third method is 0 to 10, preferably 1 to 5.

In the third method, the electron donor compound (ID) can be optionally added during the titanium treatment, wherein the amount of the internal electron donor is usually 0.005-10 mol, preferably 0.01-1 mol.

In the third method, the titanium treatment temperature is usually 0-200 ℃, preferably 30-150 ℃; the contact time is usually 1 minute to 20 hours, preferably 5 minutes to 6 hours.

According to some embodiments of the present invention, the catalyst solid component B may comprise a compound selected from, but not limited to, phthalate compounds represented by formula (IV),

in the formula (IV), R₁₅And R₁₆The same or different, each independently selected from the group consisting of a linear alkane of 1 to 20 carbon atoms, a branched alkyl of 3 to 20 carbon atoms, a cycloalkyl of 3 to 20 carbon atoms, an aryl of 6 to 20 carbon atoms, an alkaryl of 7 to 20 carbon atoms and an aralkyl of 7 to 20 carbon atoms, the alkyl, cycloalkyl, or aralkyl being a cyclic groupThe hydrogen atoms on the carbon in the alkyl, aryl, alkaryl or aralkyl group may optionally be substituted with heteroatoms, alkyl or alkoxy groups, and the carbon atoms on the alkyl, cycloalkyl, aryl, alkaryl or aralkyl backbone may optionally be substituted with heteroatoms; preferably, R₁₅And R₁₆Each independently selected from a straight chain alkyl group of 1 to 10 carbon atoms, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms, or an aryl group of 6 to 10 carbon atoms; more preferably, R₁₅And R₁₆Each independently selected from a straight chain alkyl of 1 to 6 carbon atoms or a branched alkyl of 1 to 6 carbon atoms; further preferably, R₁₅And R₁₆Each independently selected from methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl or phenyl.

Examples of suitable phthalate compounds of said formula (IV) include, but are not limited to: dimethyl phthalate, diethyl phthalate, di-n-propyl phthalate, diisopropyl phthalate, di-n-butyl phthalate, diisobutyl phthalate, di-1-methyl propyl phthalate, di-tert-butyl phthalate, di-n-pentyl phthalate, di-1-methyl butyl phthalate, di-2-methyl butyl phthalate, diisopentyl phthalate, di-1, 1' -dimethyl propyl phthalate, ditert-pentyl phthalate, di-1, 2-dimethyl propyl phthalate, n-hexyl phthalate, di-1-methyl pentyl phthalate, di-2-methyl pentyl phthalate, di-3-methyl pentyl phthalate, diisohexyl phthalate, di-isobutyl phthalate, di-n-butyl phthalate, di-isobutyl phthalate, di-1-methyl propyl phthalate, di-1-dimethyl propyl phthalate, di-n-pentyl phthalate, di-1-methyl pentyl phthalate, di-2-methyl pentyl phthalate, di-3-methyl pentyl phthalate, di-isohexyl phthalate, di-n-hexyl phthalate, di-n-butyl phthalate, di-isobutyl phthalate, di-n-butyl phthalate, di-iso-butyl phthalate, di-1-pentyl phthalate, di-1-dimethyl propyl phthalate, di-1-dimethyl-propyl phthalate, di-butyl phthalate, di-1-pentyl phthalate, di-pentyl phthalate, di-pentyl phthalate, di-pentyl, Bis (1,1 ' -dimethyl) butyl phthalate, bis (2,2 ' -dimethyl) butyl phthalate, dihexyl phthalate, bis (1, 2-dimethyl) butyl phthalate, bis (2, 3-dimethyl) butyl phthalate, bis (1,1 ', 2-trimethyl) propyl phthalate, bis (1,2,2 ' -trimethyl) propyl phthalate, n-heptyl phthalate, bis (1-methyl) hexyl phthalate, bis (2-methyl) hexyl phthalate, bis (3-methyl) hexyl phthalate, bis (4-methyl) hexyl phthalate, diisoheptyl phthalate, bis (1,1 ' -dimethyl) pentyl phthalate, Bis (2,2 '-dimethyl) pentyl phthalate, bis (3, 3' -dimethyl) pentyl phthalate, diteptyl phthalate, bis (1, 2-dimethyl) pentyl phthalate, bis (1, 3-dimethyl) pentyl phthalate, bis (1, 4-dimethyl) pentyl phthalate, bis (2, 3-dimethyl) pentyl phthalate, bis (2, 4-dimethyl) pentyl phthalate, bis (3, 4-dimethyl) pentyl phthalate, bis (1,1 ', 2-trimethyl) butyl phthalate, bis (1, 1', 3-trimethyl) butyl phthalate, bis (1,2,2 '-trimethyl) butyl phthalate, bis (2, 2', 3-trimethyl) butyl phthalate, Bis (1,3,3 '-trimethyl) butyl phthalate, bis (2,3, 3' -trimethyl) butyl phthalate, bis (1,1 ', 2, 2' -tetramethyl) propyl phthalate, n-octyl phthalate, bis (1-methyl) heptyl phthalate, bis (2-methyl) heptyl phthalate, bis (3-methyl) heptyl phthalate, bis (4-methyl) heptyl phthalate, bis (5-methyl) heptyl phthalate, diisooctyl phthalate, bis (1,1 '-dimethyl) hexyl phthalate, bis (2, 2' -dimethyl) hexyl phthalate, bis (3,3 '-dimethyl) hexyl phthalate, bis (4, 4' -dimethyl) hexyl phthalate, Bis (5,5 ' -dimethyl) hexyl phthalate, bis (1, 2-dimethyl) hexyl phthalate, bis (1, 3-dimethyl) hexyl phthalate, bis (1, 4-dimethyl) hexyl phthalate, bis (1, 5-dimethyl) hexyl phthalate, bis (2, 3-dimethyl) hexyl phthalate, bis (2, 4-dimethyl) hexyl phthalate, bis (2, 5-dimethyl) hexyl phthalate, bis (3, 4-dimethyl) hexyl phthalate, bis (3, 5-dimethyl) hexyl phthalate, bis (4, 5-dimethyl) hexyl phthalate, bis (1,1 ', 2-trimethyl) pentyl phthalate, bis (1,1 ', 3-trimethyl) pentyl phthalate, Bis (1,1 ', 4-trimethyl) pentyl phthalate, bis (1,2, 2' -trimethyl) pentyl phthalate, bis (2,2 ', 3-trimethyl) pentyl phthalate, bis (2, 2', 4-trimethyl) pentyl phthalate, bis (1,3,3 '-trimethyl) pentyl phthalate, bis (2,3, 3' -trimethyl) pentyl phthalate, bis (3,3 ', 4-trimethyl) pentyl phthalate, bis (1,4, 4' -trimethyl) pentyl phthalate, bis (2,4,4 '-trimethyl) pentyl phthalate, bis (3,4, 4' -trimethyl) pentyl phthalate, bis (1,1 ', 2, 2' -tetramethyl) butyl phthalate, bis (1,1 ', 3, 3' -tetramethyl) butyl phthalate, di (2,2 ', 3, 3' -tetramethyl) butyl phthalate, diphenyl phthalate, di (o-methyl) phenyl phthalate, di (p-methyl) phenyl phthalate, di (m-methyl) phenyl phthalate, di (o-methoxy) phenyl phthalate, di (p-methoxy) phenyl phthalate, di (m-methoxy) phenyl phthalate; preferably selected from the group consisting of dimethyl phthalate, diethyl phthalate, di-n-propyl phthalate, diisopropyl phthalate, di-n-butyl phthalate, diisobutyl phthalate, di-t-butyl phthalate, di-n-pentyl phthalate, diisopentyl phthalate, n-hexyl phthalate, diisohexyl phthalate, n-heptyl phthalate, isoheptyl phthalate, n-octyl phthalate, isooctyl phthalate, phthalic acid, diphenyl phthalate, di (o-methyl) phenyl phthalate, di (p-methyl) phenyl phthalate, di (m-methyl) phenyl phthalate, di (o-methoxy) phenyl phthalate, di (p-methoxy) phenyl phthalate, di (m-methoxy) phenyl phthalate; more preferably, the monomer is selected from dimethyl phthalate, diethyl phthalate, di-n-propyl phthalate, diisopropyl phthalate, di-n-butyl phthalate, diisobutyl phthalate, di-t-butyl phthalate, di-n-pentyl phthalate, diisopentyl phthalate, n-hexyl phthalate, isohexyl phthalate, diphenyl phthalate, di (o-methyl) phenyl phthalate, di (p-methyl) phenyl phthalate, di (o-methoxy) phenyl phthalate and di (p-methoxy) phenyl phthalate.

According to some embodiments of the present invention, the catalyst solid component B may comprise a catalyst selected from, but not limited to, glycol ester compounds represented by formula (V),

in the formula (V), R₁₇And R₁₈The same or different, and respectively is substituted or unsubstituted straight-chain C1-C20 alkyl, substituted or unsubstituted branched-chain C3-C20 alkyl, substituted or unsubstituted C3-C20 cycloalkyl, substituted or unsubstituted C6-C20 aryl, substituted or unsubstituted C7-C20 alkaryl, substituted or unsubstituted C7-C20 aralkyl, substituted or unsubstituted C2-C10 alkylene or substituted or unsubstituted C10-C20 condensed ring aryl; r₁₉-R₂₄The same or different, each is hydrogen, halogen, substituted or unsubstituted straight-chain C1-C20 alkyl, substituted or unsubstituted branched C3-C20 alkyl, substituted or unsubstituted C3-C20 cycloalkyl, substituted or unsubstituted C6-C20 aryl, substituted or unsubstituted C7-C20 alkylaryl, substituted or unsubstituted C7-C20 arylalkyl, substituted or unsubstituted C2-C10 alkenyl, or substituted or unsubstituted C10-C20 fused ring aryl; or R₁₉-R₂₂With R₂₃-R₂₄At least one of which is looped.

Examples of suitable diol ester compounds represented by the formula (V) include, but are not limited to: 2-ethyl-1, 3-propanediol dibenzoate, 2-propyl-1, 3-propanediol dibenzoate, 2-isopropyl-2-isopentyl-1, 3-propanediol dibenzoate, 1, 3-butanediol dimethylbenzoate, 2-methyl-1, 3-butanediol di-chlorobenzoate, 2, 3-dimethyl-1, 3-butanediol dibenzoate, 1, 3-pentanediol pivalate, 2, 4-pentanediol dibenzoate, 2-methyl-1, 3-pentanediol benzoate cinnamate, 2-dimethyl-1, 3-pentanediol dibenzoate, 2, 4-heptanediol dibenzoate, 3, 5-heptanediol dibenzoate, 2-isopropyl-2-isopentyl-1, 3-butanediol dibenzoate, 2-methyl-1, 3-butanediol dibenzoate, 2, 3-heptanediol dibenzoate, 2, 3-butanediol dibenzoate, 2-dimethyl-1, 3-butanediol dibenzoate, 2, 4-heptanediol dibenzoate, 2-dimethyl-1, 3-butanediol dibenzoate, 2, 3-dimethyl-1, 3-butanediol dibenzoate, 2, 3-heptanediol dibenzoate, 2, 3-diol dibenzoate, 2, 3-heptanediol dibenzoate, 2,3, or mixtures of, 3, or mixtures of any of these compounds, At least one of 4-ethyl-3, 5-heptanediol dibenzoate and 2-methyl-3, 5-heptanediol dibenzoate; preferably at least one of 3, 5-heptanediol dibenzoate, 4-ethyl-3, 5-heptanediol dibenzoate and 2, 4-pentanediol dibenzoate; more preferably 3, 5-heptanediol dibenzoate.

According to some embodiments of the present invention, the catalyst solid component B may comprise a compound selected from, but not limited to, cyanosuccinates of formula (VI),

in the formula (VI), R₂₅And R₂₆The same or different, each is independently selected from hydrogen, straight chain alkyl of 1 to 14 carbon atoms, branched alkyl of 3 to 14 carbon atoms, cycloalkyl of 3 to 10 carbon atoms, aryl of 6 to 10 carbon atoms, alkaryl of 7 to 10 carbon atoms, or aralkyl of 7 to 10 carbon atoms; r is₂₇And R₂₈The same or different, each is independently selected from a straight chain alkyl group of 1 to 10 carbon atoms, a branched alkyl group of 1 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms, an aryl group of 6 to 10 carbon atoms, an alkaryl group of 7 to 20 carbon atoms, or an aralkyl group of 7 to 20 carbon atoms.

Examples of suitable cyanosuccinates of formula (VI) include, but are not limited to: dimethyl 2, 3-diisopropyl-2-cyanosuccinate, diethyl 2, 3-diisopropyl-2-cyanosuccinate, di-n-propyl 2, 3-diisopropyl-2-cyanosuccinate, diisopropyl 2, 3-diisopropyl-2-cyanosuccinate, di-n-butyl 2, 3-diisopropyl-2-cyanosuccinate, diisobutyl 2, 3-diisopropyl-2-cyanosuccinate, and 1-methyl-4-ethyl2, 3-diisopropyl-2-cyanosuccinate (R)₂₅Methyl, R₂₆Ethyl), 2, 3-diisopropyl-2-cyanosuccinic acid-1-ethyl ester-4-methyl ester (R)₂₅Ethyl, R₂₆Methyl), 2, 3-diisopropyl-2-cyanobutanedioic acid-1-n-butyl-4-ethyl ester (R)₂₅N-butyl, R₂₆Ethyl), 2, 3-diisopropyl-2-cyanosuccinic acid-1-ethyl-4-n-butyl ester (R)₂₅Ethyl, R₂₆N-butyl), dimethyl 2, 3-diisobutyl-2-cyanosuccinate, diethyl 2, 3-diisobutyl-2-cyanosuccinate, di-n-propyl 2, 3-diisobutyl-2-cyanosuccinate, diisopropyl 2, 3-diisobutyl-2-cyanosuccinate, di-n-butyl 2, 3-diisobutyl-2-cyanosuccinate, diisobutyl 2, 3-diisobutyl-2-cyanosuccinate, and 1-methyl-4-ethyl 2, 3-diisobutyl-2-cyanosuccinate (R)₂₅Methyl, R₂₆Ethyl), 2, 3-diisobutyl-2-cyanosuccinic acid-1-ethyl-4-methyl ester (R)₂₅Ethyl, R₂₆Methyl), 2, 3-diisobutyl-2-cyanosuccinic acid-1-n-butyl-4-ethyl ester (R)₂₅N-butyl, R₂₆Ethyl), 2, 3-diisobutyl-2-cyanosuccinic acid-1-ethyl-4-n-butyl ester (R)₂₅Ethyl, R₂₆N-butyl), dimethyl 2, 3-di-sec-butyl-2-cyanosuccinate, diethyl 2, 3-di-sec-butyl-2-cyanosuccinate, di-n-propyl 2, 3-di-sec-butyl-2-cyanosuccinate, diisopropyl 2, 3-di-sec-butyl-2-cyanosuccinate, di-n-butyl 2, 3-di-sec-butyl-2-cyanosuccinate, diisobutyl 2, 3-di-sec-butyl-2-cyanosuccinate, and 1-methyl 2, 3-di-sec-butyl-2-cyanosuccinate-4-ethyl ester (R)₂₅Methyl, R₂₆Ethyl), 2, 3-di-sec-butyl-2-cyanosuccinic acid-1-ethyl-4-methyl ester (R)₂₅Ethyl, R₂₆Methyl), 2, 3-di-sec-butyl-2-cyanosuccinic acid-1-n-butyl ester-4-ethyl ester (R)₂₅N-butyl, R₂₆Ethyl), 2, 3-di-sec-butyl-2-cyanosuccinic acid-1-ethyl-4-n-butyl ester (R)₂₅Ethyl, R₂₆N-butyl), dimethyl 2, 3-dicyclopentyl-2-cyanosuccinate, diethyl 2, 3-dicyclopentyl-2-cyanosuccinate, di-n-propyl 2, 3-dicyclopentyl-2-cyanosuccinate, diisopropyl 2, 3-dicyclopentyl-2-cyanosuccinate, di-n-butyl 2, 3-dicyclopentyl-2-cyanosuccinate, diisobutyl 2, 3-dicyclopentyl-2-cyanosuccinate, and 1-methyl-4-ethyl2, 3-dicyclopentyl-2-cyanosuccinate (R)₂₅Methyl, R₂₆Ethyl), 2, 3-dicyclopentyl-2-cyanosuccinic acid-1-ethyl ester-4-methyl ester (R)₂₅Ethyl, R₂₆2 ═ methyl), 2, 3-dicyclopentyl-2-cyanosuccinic acid-1-n-butyl ester-4-ethyl ester (R)₂₅N-butyl, R₂₆Ethyl), 2, 3-dicyclopentyl-2-cyanosuccinic acid-1-ethyl-4-n-butyl ester (R)₂₅Ethyl, R₂₆N-butyl), dimethyl 2, 3-dicyclohexyl-2-cyanosuccinate, diethyl 2, 3-dicyclohexyl-2-cyanosuccinate, di-n-propyl 2, 3-dicyclohexyl-2-cyanosuccinate, diisopropyl 2, 3-dicyclohexyl-2-cyanosuccinate, and di-isopropyl 2, 3-dicyclohexyl-2-cyanosuccinateN-butyl ester, diisobutyl 2, 3-dicyclohexyl-2-cyanosuccinate, 1-methyl-2, 3-dicyclohexyl-2-cyanosuccinate-4-ethyl ester (R)₂₅Methyl, R₂₆Ethyl), 2, 3-dicyclohexyl-2-cyanosuccinic acid-1-ethyl-4-methyl ester (R)₂₅Ethyl, R₂₆Methyl), 2, 3-dicyclohexyl-2-cyanosuccinic acid-1-n-butyl ester-4-ethyl ester (R)₂₅N-butyl, R₂₆Ethyl), 2, 3-dicyclohexyl-2-cyanosuccinic acid-1-ethyl-4-n-butyl ester (R)₂₅Ethyl, R₂₆N-butyl); preferably diethyl 2, 3-diisopropyl-2-cyanosuccinate, di-n-propyl 2, 3-diisopropyl-2-cyanosuccinate, diisopropyl 2, 3-diisopropyl-2-cyanosuccinate, di-n-butyl 2, 3-diisopropyl-2-cyanosuccinate, diisobutyl 2, 3-diisopropyl-2-cyanosuccinate; more preferably diethyl 2, 3-diisopropyl-2-cyanosuccinate.

According to some embodiments of the present invention, the catalyst solid component B may comprise a compound selected from, but not limited to, diethers of formula (VII),

in the formula (VII), R₂₉And R₃₀The same or different, each independently selected from a straight chain of 1 to 10 carbon atoms or a branched chain alkyl of 3 to 10 carbon atoms; r is₃₂And R₃₃The same or different, each independently selected from a straight chain of 1 to 20 carbon atoms, a branched alkyl of 3 to 20 carbon atoms, a cycloalkyl of 3 to 20 carbon atoms, a substituted or unsubstituted aryl of 6 to 20 carbon atoms, or an alkaryl of 7 to 20 carbon atoms; r₃₁And R₃₄The same or different, each independently selected from hydrogen, straight chain alkyl of 1 to 10 carbon atoms, or branched chain alkyl of 3 to 10 carbon atoms.

Examples of suitable diethers of said formula (VII) include, but are not limited to: 2-isopropyl-2-isopentyl-1, 3-dimethoxysilane, 9-bis (methoxymethyl) fluorene, 2-isobutyl-2-isopropyl-1, 3-dimethoxypropane, 2-dicyclopentyldimethoxypropane, 2-diphenyl-1, 3-dimethoxypropane, 2-isobutyl-2-isopropyl-1, 3-dimethoxypropane, 2-dicyclopentyl-1, 3-dimethoxypropane, 2-diisobutyl-1, 3-dimethoxypropane, preferably 2-isopropyl-2-isopentyl-1, 3-dimethoxysilane, 9-bis (methoxymethyl) fluorene.

According to some embodiments of the present invention, the catalyst solid component B may comprise a compound selected from, but not limited to, succinates represented by formula (VIII),

in the formula (VIII), R₃₅And R₃₆The same or different, each independently selected from a straight chain alkyl group of 1 to 20 carbon atoms, a branched alkyl group of 3 to 20 carbon atoms, an alkenyl group of 2 to 20 carbon atoms, a cycloalkyl group of 3 to 20 carbon atoms, an aryl group of 6 to 20 carbon atoms, an aralkyl group of 7 to 20 carbon atoms or an alkaryl group of 7 to 20 carbon atoms; r₃₇-R₄₀The same or different from each other, each independently selected from hydrogen, a straight chain alkyl group of 1 to 20 carbon atoms, a branched alkyl group of 3 to 20 carbon atoms, an alkenyl group of 2 to 20 carbon atoms, a cycloalkyl group of 3 to 20 carbon atoms, an aryl group of 6 to 20 carbon atoms, an aralkyl group of 7 to 20 carbon atoms or an alkaryl group of 7 to 20 carbon atoms; the R is₃₅And R₃₆Optionally containing heteroatoms.

Examples of suitable succinate compounds of formula (VIII) include, but are not limited to: diethyl 2, 3-bis (2-ethylbutyl) succinate, diethyl 2, 3-diethyl-2-isopropylsuccinate, diethyl 2, 3-diisopropylsuccinate, diethyl 2, 3-di-tert-butylsuccinate, diethyl 2, 3-diisobutylsuccinate, diethyl 2,3- (bistrimethylsilyl) succinate, diethyl 2- (, 3,3, 3-trifluoropropyl) -3-methylsuccinate, diethyl 2, 3-dineopentylsuccinate, diethyl 2, 3-diisopentylsuccinate, diethyl 2,3- (1-trifluoromethyl-ethyl) succinate, diethyl 2-isopropyl-3-isobutylsuccinate, diethyl 2-tert-butyl-3-isopropylsuccinate, diethyl 2-isopropyl-3-cyclohexylsuccinate, diethyl 2-isopentyl-3-cyclohexylsuccinate, diethyl 2,2,3, 3-methylsuccinate, diethyl 2,2,3, 3-tetraethylsuccinate, diethyl 2,2,3, 3-tetrapropylsuccinate, diethyl 2, 3-diethyl-2, 3-diisopropylsuccinate, diisobutyl 2, 3-bis (2-ethylbutyl) succinate, diisobutyl 2, 3-diethyl-2-isopropylsuccinate, diisobutyl 2, 3-diisopropylsuccinate, diisobutyl 2, 3-di-tert-butylsuccinate, diisobutyl 2, 3-diisobutylsuccinate, diisobutyl 2,3- (bistrimethylsilyl) succinate, diisobutyl 2- (, 3,3, 3-trifluoropropyl) -3-methylsuccinate, diisobutyl 2, 3-dineopentylsuccinate, diisobutyl 2, 3-diisopentylsuccinate, diisobutyl 2,3- (1-trifluoromethyl-ethyl) succinate, diisobutyl 2-isopropyl-3-isobutylsuccinate, diisobutyl 2-tert-butyl-3-isopropylsuccinate, diisobutyl 2-isopropyl-3-cyclohexylsuccinate, diisobutyl 2-isopentyl-3-cyclohexylsuccinate, diisobutyl 2,2,3, 3-methylsuccinate, diisobutyl 2,2,3, 3-tetraethylsuccinate, diisobutyl 2,2,3, 3-diisopropyl-2, 3-diisopropyl-3-di-isopropyl-3-butanedioic acid isobutyl ester; preferably 2, 3-diisopropyl succinate diethyl ester, 2, 3-di-tert-butyl succinate diethyl ester, 2, 3-diisobutyl succinate diethyl ester, 2, 3-diisopropyl succinate diisobutyl ester; 2, 3-diisopropylsuccinate.

According to the invention, in the solid component B of the catalyst, the compound of the internal electron donor can be used alone, or two or more internal electron donor compounds can be used in a composite way.

In a preferred case, the alkylaluminum compound may be a compound represented by formula (IX),

AlR'_n'X'_3-n' (IX)

wherein R' is one of the following substances: hydrogen, alkyl with 1-20 carbon atoms or aryl with 6-20 carbon atoms; x 'is halogen, and n' is an integer of 1 to 3.

The alkyl aluminum compound is preferably selected from at least one of the following compounds: at least one of trimethylaluminum, triethylaluminum, triisobutylaluminum, trioctylaluminum, diethylaluminum monohydrogen, diisobutylaluminum monohydrogen, diethylaluminum monochloride, diisobutylaluminum monochloride, ethylaluminum sesquichloride and ethylaluminum dichlorochloride. More preferably triethylaluminium and/or triisobutylaluminium.

The alkyl aluminum compound may be used in amounts conventional in the art. Generally, the molar ratio of aluminum in the aluminum alkyl compound C to titanium in the solid catalyst composition is from 5 to 5000: 1; preferably 20 to 1000: 1; more preferably 50 to 500: 1.

according to some embodiments of the invention, the ratio of the total number of moles of aluminium in the alkylaluminium compound C and of the external electron donor a is between 0.5-1 and 50: 1, preferably 1 to 30: 1, more preferably 1 to 20: 1.

in a third aspect, the present invention provides a process for the polymerisation of olefins comprising contacting one or more olefins with a catalyst system as described in the second aspect to give a polymer. Wherein at least one of the olefins is represented by the general formula CH₂An alkene represented by ═ CHR, where R is selected from hydrogen or alkyl of 1 to 6 carbon atoms.

The olefin polymerization method can be used for olefin homopolymerization and can also be used for copolymerizing a plurality of olefins.

According to some embodiments of the present invention, the olefin is preferably selected from at least one of ethylene, propylene, 1-n-butene, 1-n-pentene, 1-n-hexene, 1-n-octene, and 4-methyl-1-pentene; more preferably at least one selected from the group consisting of ethylene, propylene and 1-butene.

The olefin polymerization process according to the invention, the olefin polymerization conditions comprising: the temperature of the olefin polymerization is from 0 to 150 ℃, preferably from 60 to 130 ℃; the time is 0.1 to 5 hours, preferably 0.5 to 4 hours, and the pressure is 0.01 to 10MPa, preferably 0.5 to 5 MPa. The amount of catalyst used may be any of the various catalysts known in the art.

The invention can obtain the catalyst with excellent comprehensive performance by adopting novel external electron donor, and when the catalyst is used for propylene polymerization, the catalyst has high polymerization activity, good hydrogen regulation sensitivity and higher stereospecificity. Meanwhile, the catalyst has the performance of high-temperature self-inactivation.

Detailed Description

The following examples are given for the purpose of illustrating the invention and are not to be construed as limiting the invention.

The test method comprises the following steps:

1. titanium content in catalyst: tested according to 721 spectrophotometer.

2. The particle size distribution of the catalyst is as follows: measured according to the malvern 2000 n-hexane dispersant laser diffraction method.

3. Determination of the melt index of the Polymer: measured according to GB/T3682-2000.

4. Polymer isotacticity was determined using heptane extraction: a2 g sample of the dried polymer was extracted with boiling heptane in an extractor for 6 hours, and the ratio of the weight (g) of the polymer to 2(g) of the residue was dried to a constant weight, which was the isotacticity.

The embodiment is as follows:

firstly, synthesizing an electron donor compound:

compound a1 ethyl N, N-di-N-butylaminoacetate

1000mL three-necked flask was charged with di-n-butylamine (77.4 g, 0.6mol) and K₂CO₃(82.8 g, 60mmol), KI (1.8 g, 12mmol) and acetonitrile 400 mL. Ethyl bromoacetate (85.8 g, 0.51mmol) was added dropwise. The reaction was refluxed for 8 hours. And (5) finishing the reaction. And (5) cooling the system. Filtering and desalting. The solid was washed with 2X 100mL of dichloromethane. The organic phase was washed with 2X 100mL of saturated brine. The organic phase was dried over anhydrous sodium sulfate and filtered. The solvent is removed by reduced pressure distillation and the product is obtained by rectification (5mmHg,64 ℃).

¹HNMR(CDCl₃/TMS,300MHz)δ(ppm):0.67-0.88(t,6H,-N CH₂CH₂CH₂CH₃),1.05-1.17(q,4H,-NCH₂CH₂CH₂CH₃),1.20-1.29(tetra,3H,-COOCH₂CH₃)，1.20-1.49(m,4H,-NCH₂CH₂CH₂CH₃),2.30-2.70(m,4H,-NCH₂CH₂CH₂CH₃),3.30(s,2H,-NCH₂COOEt)，4.13(tetra,2H,-COOCH₂CH₃)。

Compound a 2N, N-di-N-octylglycine ethyl ester

Using a method similar to that for compound a1, ethyl N, N-di-N-octylaminoacetate was prepared.

¹H NMR(CDCl₃/TMS,300MHz)0.86-0.93(m,6H,-N C₇H₁₄CH₃),1.27(tetra,3H,-COOCH₂CH₃)，1.27(m,20H,-NCH₂CH₂C₅H₁₀CH₃),1.49(m,4H,-NCH₂CH₂C₅H₁₀CH₃)，2.30-2.60(m,4H,-NCH₂C₇H₁₅),3.30(s,2H,-NCH₂COOEt)，4.13(tetra,2H,-COOCH₂CH₃)。

Compound a 3N, N-diisooctylamino acetic acid ethyl ester

Using a method similar to that of Compound a1, ethyl N, N-diisooctylaminoacetate was prepared.

¹H NMR(CDCl₃/TMS,300MHz)0.89-0.93(m,6H,-NCH₂CH(CH₂CH₃)C₄H₈CH₃),1.27(m,3H,-COOCH₂CH₃)，1.27(m,16H,-NCH₂CH(CH₂CH₃)C₄H₈CH₃),1.53(m,4H,-NCH₂CH(CH₂CH₃)C₄H₁₆CH₃)，1.71(m,2H,-NCH₂CH(CH₂CH₃)C₄H₁₆CH₃)，2.30-2.60(m,4H,-NCH₂C₇H₁₅),3.30(s,2H,-NCH₂COOEt)，4.13(tetra,2H,-COOCH₂CH₃)。

Compound a 4N, N-diallylaminoacetic acid butyl ester

Butyl N, N-diallylaminoacetate is prepared in a similar manner to compound a1, starting from butyl chloroethylene.

¹H NMR(CDCl₃/TMS,300MHz)0.86-0.91(t,3H,-OCH₂CH₂CH₂CH₃),1.37-1.50(m,2H,-OCH₂CH₂CH₂CH₃)，1.57-1.66(m,2H,-OCH₂CH₂CH₂CH₃),3.23-3.25(d,2H,-NCH₂CH＝CH₂)，3.31(s,2H,-NCH₂COO-)，4.03-4.07(t,2H,--OCH₂CH₂CH₂CH₃),5.11-5.17(m,2H,2H,-NCH₂CH＝CH₂)，5.79-5.93(m,1H,-NCH₂CH＝CH₂)。

Preparation of solid catalyst component

Preparatory example 1

After a 16L pressure-resistant reactor equipped with a stirrer was sufficiently replaced with nitrogen, 10L of ethanol, 300ml of 2-ethylhexanol, 11.2g of iodine, 8g of magnesium chloride and 640g of magnesium powder were charged into the reactor. The system was refluxed with stirring until no more hydrogen was vented. The reaction was stopped, washed three times with 3L ethanol, filtered and dried. The obtained alkoxy magnesium carrier. The obtained alkoxy magnesium carrier D50 is 30.2um, Span value is 0.81, and m value is 0.015.

Preparation of solid catalyst Components 1-4:

taking 10g of the alkoxy magnesium carrier prepared in the preparation example and 50mL of toluene, and adding 10mmol of the electron donor compound shown in the table 1 to prepare suspension; adding 40mL of toluene and 60mL of titanium tetrachloride into a 300mL reaction kettle repeatedly replaced by high-purity nitrogen, then adding the prepared suspension into the kettle, heating to 80 ℃, keeping the temperature for 1 hour, then continuously heating to 115 ℃, keeping the temperature for 2 hours, and then carrying out pressure filtration on the liquid (mother liquor) to be clean. Adding 90mL of mixed solution of toluene and 60mL of titanium tetrachloride, heating to 110 ℃, stirring for 1 hour (titanium treatment), carrying out filter pressing on the liquid (mother solution), adding 120mL of mixed solution of toluene and 30mL of titanium tetrachloride, heating to 110 ℃, stirring for 2 hours (titanium treatment), filtering out the liquid, washing the obtained solid with 150mL of n-hexane for 3 times at 55 ℃, washing with n-hexane once at room temperature, filtering out the liquid and drying to obtain the solid catalyst component.

Preparation of catalyst solid component 5:

3.150mol (300.0g) of anhydrous magnesium chloride, 19.68mol (2.1L) of toluene and 8.4mol (1.1L) of 2-ethylhexanol are sequentially added into a reaction kettle repeatedly replaced by high-purity nitrogen, and the mixture reacts for 3.0 hours under the conditions that the stirring speed is 450rpm and the temperature is 115 ℃ to obtain a stable and uniform alcohol compound solution; then, 84mmol (42ml) of 3, 5-heptanediol dibenzoate and 260mmol (60ml) of diphenyldimethoxysilane were added thereto, and the mixture was stirred for 60 minutes and cooled to room temperature.

Adding the uniform alcohol compound solution added with 84mmol (42ml) of 3, 5-heptanediol dibenzoate and 260mmol (60ml) of diphenyl dimethoxysilane into a reactor which is fully replaced by nitrogen and is filled with 60mol (6.6L) of titanium tetrachloride and 11.4mol (1.2L) of toluene at the temperature of-20 ℃, fully contacting the mixture at the temperature of-20 ℃ by stirring, heating the mixture to 100 ℃ after 5 hours, separating out solid precipitates in the heating process, adding 138.6mmol (30g) of 2-isopropyl-2-isoamyl-1, 3-dimethoxypropane, reacting for 1 hour, and filtering out liquid after the reaction is finished; then the solid was contacted with 40.8mol (4.32L) of toluene, 26.2mol (2.88ml) of titanium tetrachloride and 193.8mmol (42g) of 2-isopropyl-2-isopentyl-1, 3-dimethoxypropane at 100 ℃ for 1.5 hours, and after the reaction was completed, the liquid was filtered off; the solid was then contacted with 40.8mol (4.32L) of toluene and 26.2mol (2.88ml) of titanium tetrachloride at 110 ℃ for a further 0.5 hour; after the reaction was completed, the liquid was filtered off and the contact reaction with 40.8mol (4.32L) of toluene and 26.2mol (2.88ml) of titanium tetrachloride at 110 ℃ was repeated once more. The resulting solid was washed 5 times with 55.14mol (7.2L) of hexane and then dried to obtain an olefin polymerization catalyst solid component 5.

TABLE 1. kinds and amounts of internal electron donors in different examples

Examples 1 to 24

After sufficient replacement with vapor phase propylene in a 5L autoclave, 1L of liquid propylene, 5mL of a hexane solution of triethylaluminum (the concentration of triethylaluminum is 0.5mmol/mL) was added at room temperature, the temperature was raised to 50 ℃ and 2mL of a hexane solution of an external electron donor shown in Table 2 (the concentration of triethylaluminum is 0.10mmol/mL), 10mL of anhydrous hexane and 10mg of a solid catalyst component, 0.9 standard L of hydrogen and 2L of liquid propylene were added; the temperature was raised to the polymerization temperature shown in Table 2 within 10 minutes under stirring, and after polymerization at this temperature for 1 hour, the stirring was stopped, the unpolymerized propylene monomer was removed, and the polymer was collected.

Comparative examples 1 to 12

The specific procedure is as in examples 1-10, except that the external electron donor is replaced by methylcyclohexyldimethoxysilane.

TABLE 2 Performance of the catalyst

As can be seen from the data in Table 2, when the catalyst containing the amino ester compound and the siloxane compound is used as an external electron donor for propylene polymerization, the catalyst has high polymerization activity, good hydrogen response and stereospecific capacity, and good high-temperature self-deactivation property, and is beneficial to the application of the catalyst in industrial devices.

Any numerical value mentioned in this specification, if there is only a two unit interval between any lowest value and any highest value, includes all values from the lowest value to the highest value incremented by one unit at a time. For example, if it is stated that the amount of a component, or a value of a process variable such as temperature, pressure, time, etc., is 50 to 90, it is meant in this specification that values of 51 to 89, 52 to 88 … …, and 69 to 71, and 70 to 71, etc., are specifically enumerated. For non-integer values, units of 0.1, 0.01, 0.001, or 0.0001 may be considered as appropriate. These are only some specifically named examples. In a similar manner, all possible combinations of numerical values between the lowest value and the highest value enumerated are to be considered to be disclosed in this application.

It should be noted that the above-mentioned embodiments are only for explaining the present invention, and do not constitute any limitation to the present invention. The present invention has been described with reference to exemplary embodiments, but the words which have been used herein are words of description and illustration, rather than words of limitation. The invention can be modified, as prescribed, within the scope of the claims and without departing from the scope and spirit of the invention. Although the invention has been described herein with reference to particular means, materials and embodiments, the invention is not intended to be limited to the particulars disclosed herein, but rather extends to all other methods and applications having the same functionality.

Claims

1. An external electron donor for olefin polymerization, which comprises an amino ester compound shown as a formula (I) and a siloxane compound shown as a formula (II),

R₄and R₅Is the same as orDifferent, each independently selected from the group consisting of a linear alkane of 1 to 20 carbon atoms, a branched alkyl of 3 to 20 carbon atoms, a cycloalkyl of 3 to 20 carbon atoms, an aryl of 6 to 20 carbon atoms, an alkaryl of 7 to 20 carbon atoms, or an aralkyl of 7 to 20 carbon atoms, the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl groups having carbon atoms in the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl group optionally substituted or unsubstituted with heteroatoms, alkyl, or alkoxy groups, the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl group having carbon atoms in the backbone optionally substituted or unsubstituted with heteroatoms;

R₁”_m”R₂”_n”Si(OR_3”)_4-m”-n” (II)

in the formula (II), R₁"and R₂"is the same or different and is each independently selected from the group consisting of halogen, hydrogen, straight chain alkyl of 1 to 20 carbon atoms, branched alkyl of 3 to 20 carbon atoms, cycloalkyl of 3 to 20 carbon atoms, aryl of 6 to 20 carbon atoms, and haloalkyl of 1 to 20 carbon atoms; r3' is selected from straight chain alkyl group with 1-20 carbon atoms, branched chain alkyl group with 3-20 carbon atoms, naphthenic group with 3-20 carbon atoms, aryl group with 6-20 carbon atoms or halogenated alkyl group with 1-20 carbon atoms; m "and n" are each independently selected from integers of 0-3, and m "+ n"<4。

2. A catalyst system for the polymerization of olefins comprising

(1) An external electron donor A;

(3) an alkylaluminum compound C as a cocatalyst;

in the formula (I), R₁Selected from linear alkanes of 1 to 20 carbon atoms, branched alkyl of 3 to 20 carbon atomsCycloalkyl of 3 to 20 carbon atoms, aryl of 6 to 20 carbon atoms, alkylaryl of 7 to 20 carbon atoms or arylalkyl of 7 to 20 carbon atoms, wherein the hydrogen atoms in the carbon of said alkyl, cycloalkyl, arylalkyl, alkylaryl or arylalkyl groups are optionally substituted or unsubstituted by heteroatoms, alkyl or alkoxy groups, and the carbon atoms in the backbone of said alkyl, cycloalkyl, arylalkyl, alkylaryl or arylalkyl groups are optionally substituted or unsubstituted by heteroatoms;

R₄and R₅The same or different, each independently selected from the group consisting of a linear alkane of 1 to 20 carbon atoms, a branched alkyl of 3 to 20 carbon atoms, a cycloalkyl of 3 to 20 carbon atoms, an aryl of 6 to 20 carbon atoms, an alkaryl of 7 to 20 carbon atoms, or an aralkyl of 7 to 20 carbon atoms, the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl groups having the hydrogen atoms on the carbon optionally substituted or unsubstituted by heteroatoms, alkyl groups, or alkoxy groups, the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl groups having the carbon atoms on the backbone optionally substituted or unsubstituted by heteroatoms;

R₁”_m”R₂”_n”Si(OR_3”)_4-m”-n” (II)

in the formula (II), R₁"and R₂"same or different, each independently selected from halogen, hydrogen atom, straight chain alkyl of 1 to 20 carbon atoms, branched chain alkyl of 3 to 20 carbon atoms, cycloalkyl of 3 to 20 carbon atoms, aryl of 6 to 20 carbon atoms orHaloalkyl of 1 to 20 carbon atoms; r3' is selected from straight chain alkyl group with 1-20 carbon atoms, branched chain alkyl group with 3-20 carbon atoms, naphthenic group with 3-20 carbon atoms, aryl group with 6-20 carbon atoms or halogenated alkyl group with 1-20 carbon atoms; m "and n" are each independently selected from integers of 0-3, and m "+ n"<4。

3. An external electron donor according to claim 1 or a catalyst system according to claim 2, wherein in formula (I), R is₁Selected from a straight chain alkyl group of 1 to 10 carbon atoms, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms, an aryl group of 6 to 10 carbon atoms, an alkaryl group of 7 to 10 carbon atoms, or an aralkyl group of 7 to 10 carbon atoms;

R₂and R₃Independently selected from a linear alkyl group of 3 to 10 carbon atoms, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms or an aryl group of 6 to 20 carbon atoms, preferably R₂And R₃Independently selected from a straight chain alkyl of 1 to 6 carbon atoms or a branched alkyl of 3 to 6 carbon atoms;

R₄and R₅Independently selected from a linear alkyl group of 1 to 10 carbon atoms, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms or an aryl group of 6 to 10 carbon atoms, preferably R₄And R₅Independently selected from a straight chain alkyl group of 1 to 6 carbon atoms or a branched alkyl group of 3 to 6 carbon atoms, further preferably R₄And R₅Independently selected from hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl or phenyl; and/or

The heteroatom comprises a halogen atom; and/or when R₂And R₃When linked to form a ring, the resulting ring may or may not contain double bonds or heteroatoms in the backbone.

4. The external electron donor of claim 1 or the catalyst system of claim 2 or 3, wherein in formula (II), R is₁"and R₂Each independently selected from halogen, hydrogen atom, straight chain of 1-10 carbon atomsAn alkyl group, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms, an aryl group of 6 to 10 carbon atoms or a haloalkyl group of 1 to 10 carbon atoms; r3' is selected from straight chain alkyl of 1-10 carbon atoms, branched alkyl of 3-10 carbon atoms, cycloalkyl of 3-10 carbon atoms, aryl of 6-10 carbon atoms or halogenated alkyl of 1-10 carbon atoms.

5. The external electron donor of claim 1 or the catalyst system of any one of claims 2-4, wherein the amino ester compound is selected from at least one of the following compounds: ethyl N, N-dipropylaminoacetate, propyl N, N-dipropylaminoacetate, butyl N, N-dipropylaminoacetate, isobutyl N, N-dipropylaminoacetate, 1-pentanol N, N-dipropylaminoacetate, 1-hexanol N, N-dipropylaminoacetate, 1-heptanol N, N-dipropylaminoacetate, 1-octanol N, N-dipropylaminoacetate, 1-nonanol N, N-dipropylaminoacetate, 1-decanol N, N-dipropylaminoacetate, phenol N, N-dipropylaminoacetate, o-methylphenol N, N-dipropylaminoacetate, butyl N, N-diallylaminoacetate, ethyl N, N-dibutylaminoacetate, butyl N, N-dipropylaminoacetate, butyl N-dipropylaminoacetate, N-1-heptanol N, N-dipropylaminoacetate, N-1-octanol N, N-dipropylaminoacetate, N-1-octanol, N-dipropylaminoacetate, butyl acetate, N-dipropylaminoacetate, N-isopropylacetate, N-1-isopropylamide, N-isopropylamino-acetate, N-isopropylamino-N-isopropylamino-and a, Propyl N, N-dibutylaminoacetate, butyl N, N-dibutylaminoacetate, isobutyl N, N-dibutylaminoacetate, 1-pentanol N, N-dibutylaminoacetate, 1-hexanol N, N-dibutylaminoacetate, 1-heptanol N, N-dibutylaminoacetate, 1-octanol N, N-dibutylaminoacetate, 1-nonanol N, N-dibutylaminoacetate, 1-decanol N, N-dibutylaminoacetate, phenol N, N-dibutylaminoacetate, o-methylphenol N, N-dibutylaminoacetate, ethyl N, N-dipentylaminoacetate, propyl N, N-dipentylaminoacetate, butyl N, N-dipentylaminoacetate, Isobutyl N, N-dipentylaminoacetate, 1-pentanol N, N-dipentylaminoacetate, 1-hexanol N, N-dipentylaminoacetate, 1-heptanol N, N-dipentylaminoacetate, 1-octanol N, N-dipentylaminoacetate, 1-nonanol N, N-dipentylaminoacetate, 1-decanol N, N-dipentylaminoacetate, phenol N, N-dipentylaminoacetate, o-methylphenol N, N-dipentylaminoacetate, ethyl N, N-dihexylaminoacetate, propyl N, N-dihexylaminoacetate, butyl N, N-dihexylaminoacetate, isobutyl N-dihexylaminoacetate, 1-pentanol N, N-dihexylaminoacetate, tert-butylaminoacetate, N-dihexylaminoacetate, 1-pentanol N, N-dihexylaminoacetate, or mixtures thereof, 1-hexanol N, N-dihexylaminoacetate, 1-heptanol N, N-dihexylaminoacetate, 1-octanol N, N-dihexylaminoacetate, 1-nonanol N, N-dihexylaminoacetate, 1-decanol N, N-dihexylaminoacetate, phenol N, N-dihexylaminoacetate, o-methylphenol N, N-dihexylaminoacetate, ethyl N, N-dihexylaminoacetate, propyl N, N-dihexylaminoacetate, butyl N, N-dihexylaminoacetate, isobutyl N-dihexylaminoacetate, 1-pentanol N, N-dihexylaminoacetate, 1-hexanol N, N-dihexylaminoacetate, N, N-1-heptylaminoacetic acid-1-heptanol ester, N-1-octanylglycine-1-octanol ester, N-1-nonane-, N-1-decanol-, phenol-, o-methylphenol-, ethyl-, propyl-, butyl-, isobutyl-, 1-pentanol-, N-dioctylaminoacetic acid-1-pentanol ester, N-1-hexanol-, 1-heptanol-, N-dioctylaminoacetic acid-1-heptanol ester, 1-octyl N, N-dioctylaminoacetate, 1-nonyl N, N-dioctylaminoacetate, 1-decyl N, N-dioctylaminoacetate, phenol N, N-dioctylaminoacetate, o-methylphenol N, N-dioctylaminoacetate, ethyl N, N-di-isooctylaminoacetate, propyl N, N-di-isooctylaminoacetate, butyl N, N-di-isooctylaminoacetate, isobutyl N, N-di-isooctylaminoacetate, 1-pentyl N, N-di-isooctylaminoacetate, 1-hexyl N, N-di-isooctylaminoacetate, 1-heptyl N, N-di-isooctylaminoacetate, 1-octyl alcohol N, N-di-isooctylaminoacetate, 1-nonyl N, N-diisooctylaminoacetate, 1-decyl N, N-diisooctylaminoacetate, phenol N, N-diisooctylaminoacetate, o-cresol N, N-diisooctylaminoacetate, ethyl N, N-dinonylaminoacetate, propyl N, N-dinonylaminoacetate, butyl N, N-dinonylaminoacetate, isobutyl N, N-dinonylaminoacetate, 1-amyl N, N-dinonylaminoacetate, 1-hexyl N, N-dinonylaminoacetate, 1-heptyl N, N-dinonylaminoacetate, 1-octyl N, N-dinonylaminoacetate, 1-nonyl N, N-dinonylaminoacetate, 1-decyl N, N-dinonylaminoacetic acid, phenol N, N-dinonylaminoacetic acid, o-methyl phenol N, N-didecylaminoacetic acid, ethyl N, N-didecylaminoacetic acid, propyl N, N-didecylaminoacetic acid, butyl N, N-didecylaminoacetic acid, isobutyl N, N-didecylaminoacetic acid, 1-pentyl N, N-didecylaminoacetic acid, 1-hexyl N, N-didecylaminoacetic acid, 1-heptyl N, N-didecylaminoacetic acid, 1-octyl N, N-didecylaminoacetic acid, 1-nonyl N, N-didecylaminoacetic acid, 1-decyl N, N-didecylaminoacetic acid, Phenol N, N-didecyl amino acetate and o-methyl phenol N, N-didecyl amino acetate.

6. Catalyst system according to any of claims 2 to 5, characterized in that the siloxane-based compound is selected from the group consisting of trimethylmethoxysilane, diisopropyldimethoxysilane, diisobutyldimethoxysilane, isopropylisobutyldimethoxysilane, di-tert-butyldimethoxysilane, tert-butylmethyldimethoxysilane, tert-butylethyldimethoxysilane, tert-butylpropyldimethoxysilane, tert-butylisopropyldimethoxysilane, cyclohexylmethyldimethoxysilane, dicyclohexyldimethoxysilane, cyclohexyl-tert-butyldimethoxysilane, cyclopentylmethyl-dimethoxysilane, cyclopentylethyldimethoxysilane, dicyclopentyldimethoxysilane, cyclopentylcyclohexyldimethoxysilane, bis (2-methylcyclopentyl) dimethoxysilane, diphenyldimethoxysilane, di-tert-butyldimethoxysilane, cyclopentyldimethoxysilane, di-tert-butyldimethoxysilane, di-ethyldimethoxysilane, dicyclopentyldimethoxysilane, cyclopentyldimethoxysilane, bis (2-methylcyclopentyl) dimethoxysilane, di-hexyldimethoxysilane, di-methoxysilane, di-butyldimethoxysilane, di-tert-butyldimethoxysilane, di-2-butyldimethoxysilane, di-tert-butyldimethoxysilane, di-2-butyldimethoxysilane, di-butylsilane, di-tert-butyldimethoxysilane, di-butylsilane, di-2-butyldimethoxysilane, di-butylsilane, di-or-butylsilane, di-2-butyldimethoxysilane, di-2-butyldimethoxysilane, and a-butylsilane, di-or-butylsilane, and a-bis (2-butylsilane, At least one of diphenyldiethoxysilane, phenyltriethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, isopropyltrimethoxysilane, isopropyltriethoxysilane, butyltrimethoxysilane, butyltriethoxysilane, isobutyltrimethoxysilane, isobutyltriethoxysilane, pentyltrimethoxysilane, isopentyltrimethoxysilane, cyclopentyltrimethoxysilane, cyclohexyltrimethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, tetramethoxysilane, tetraethoxysilane, and tetrabutoxysilane.

7. Catalyst system according to any of claims 2-6, characterized in that the amino ester compound constitutes 5-95 mol%, preferably 5-60 mol%, more preferably 10-40 mol% of the external electron donor A.

8. The catalyst system according to any one of claims 2 to 7, wherein the internal electron donor compound is at least one selected from the group consisting of phthalate-based compounds, glycol-based compounds, cyanosuccinate-based compounds, diether-based compounds, and succinate-based compounds; preferably at least one selected from the group consisting of glycol ester compounds, cyanosuccinate compounds, diether compounds and succinate compounds; more preferably from the diether class of compounds.

9. The catalyst system according to any of claims 2 to 8, wherein the phthalate compound is selected from the phthalate compounds of formula (IV),

in the formula (IV), R₁₅And R₁₆The same or different, each independently selected from the group consisting of a linear alkane of 1 to 20 carbon atoms, a branched alkyl of 3 to 20 carbon atoms, a cycloalkyl of 3 to 20 carbon atoms, an aryl of 6 to 20 carbon atoms, an alkaryl of 7 to 20 carbon atoms, or an aralkyl of 7 to 20 carbon atoms, the hydrogen atoms on the carbons of the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl groups optionally being substituted with heteroatoms, alkyl groups, or alkoxy groups, the carbon atoms on the alkyl, cycloalkyl, aryl, alkaryl, or aralkyl backbone optionally being substituted with heteroatoms; preferably, R₁₅And R₁₆Each independently selected from a straight chain alkyl group of 1 to 10 carbon atoms, a branched alkyl group of 3 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms, or an aryl group of 6 to 10 carbon atoms; more preferably, R₁₅And R₁₆Each independently selected from 1 to 6 carbon atomsStraight chain alkyl or branched alkyl of 1 to 6 carbon atoms; further preferably, R₁₅And R₁₆Each independently selected from methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl or phenyl;

the diol ester compound is selected from the diol ester compounds shown in the formula (V),

in the formula (V), R₁₇And R₁₈The same or different, each being a substituted or unsubstituted linear alkane of 1 to 20 carbon atoms, a substituted or unsubstituted branched alkyl of 3 to 20 carbon atoms, a substituted or unsubstituted cycloalkyl of 3 to 20 carbon atoms, a substituted or unsubstituted aryl of 6 to 20 carbon atoms, a substituted or unsubstituted alkylaryl of 7 to 20 carbon atoms, a substituted or unsubstituted arylalkyl of 7 to 20 carbon atoms, a substituted or unsubstituted alkylene of 2 to 10 carbon atoms, or a substituted or unsubstituted fused ring aryl of 10 to 20 carbon atoms; r₁₉-R₂₄The same or different, each being hydrogen, halogen, a substituted or unsubstituted straight-chain linear alkyl group of 1 to 20 carbon atoms, a substituted or unsubstituted branched alkyl group of 3 to 20 carbon atoms, a substituted or unsubstituted cycloalkyl group of 3 to 20 carbon atoms, a substituted or unsubstituted aryl group of 6 to 20 carbon atoms, a substituted or unsubstituted alkylaryl group of 7 to 20 carbon atoms, a substituted or unsubstituted arylalkyl group of 7 to 20 carbon atoms, a substituted or unsubstituted alkylene group of 2 to 10 carbon atoms, or a substituted or unsubstituted fused ring aryl group of 10 to 20 carbon atoms, respectively; or R₁₉-R₂₂With R₂₃-R₂₄Looping at least one of the loops;

the cyanosuccinate compound is selected from the cyanosuccinate compound shown in the formula (VI),

in the formula (VI), R₂₅And R₂₆The same or different, each is independently selected from hydrogen, straight chain alkyl of 1 to 14 carbon atoms, branched alkyl of 3 to 14 carbon atoms, cycloalkyl of 3 to 10 carbon atoms, aryl of 6 to 10 carbon atoms, alkaryl of 7 to 10 carbon atoms, or aralkyl of 7 to 10 carbon atoms; r₂₇And R₂₈The same or different, each independently selected from a straight chain alkyl group of 1 to 10 carbon atoms, a branched alkyl group of 1 to 10 carbon atoms, a cycloalkyl group of 3 to 10 carbon atoms, an aryl group of 6 to 10 carbon atoms, an alkaryl group of 7 to 20 carbon atoms, or an aralkyl group of 7 to 20 carbon atoms;

the diether compound is selected from diether compounds shown in a formula (VII),

in the formula (VII), R₂₉And R₃₀The same or different, each independently selected from a straight chain of 1 to 10 carbon atoms or a branched chain alkyl of 3 to 10 carbon atoms; r₃₂And R₃₃The same or different, each independently selected from the group consisting of a straight chain of 1 to 20 carbon atoms, a branched alkyl of 3 to 20 carbon atoms, a cycloalkyl of 3 to 20 carbon atoms, a substituted or unsubstituted aryl of 6 to 20 carbon atoms, or an alkaryl of 7 to 20 carbon atoms; r₃₁And R₃₄The same or different, each independently selected from hydrogen, straight chain alkyl of 1 to 10 carbon atoms, or branched chain alkyl of 3 to 10 carbon atoms;

the succinate compound is selected from succinate compounds shown in a formula (VIII),

in the formula (VIII), R₃₅And R₃₆The same or different, each independently selected from the group consisting of straight chain alkyl of 1 to 20 carbon atoms, branched alkyl of 3 to 20 carbon atoms, alkenyl of 2 to 20 carbon atoms, cycloalkyl of 3 to 20 carbon atoms, and aryl of 6 to 20 carbon atomsA group, an aralkyl group of 7 to 20 carbon atoms or an alkaryl group of 7 to 20 carbon atoms; r₃₇-R₄₀The same or different from each other, each independently selected from hydrogen, a straight chain alkyl group of 1 to 20 carbon atoms, a branched alkyl group of 3 to 20 carbon atoms, an alkenyl group of 2 to 20 carbon atoms, a cycloalkyl group of 3 to 20 carbon atoms, an aryl group of 6 to 20 carbon atoms, an aralkyl group of 7 to 20 carbon atoms or an alkaryl group of 7 to 20 carbon atoms; the R is₃₅And R₃₆Optionally containing heteroatoms.

10. Catalyst system according to any of claims 2 to 9, characterized in that the alkylaluminum compound is selected from the compounds of formula (IX),

AlR'_n'X'_3-n' (IX)

in formula (IX), R' is selected from hydrogen, alkyl of 1 to 20 carbon atoms or aryl of 6 to 20 carbon atoms; x 'is selected from halogen, n' is an integer of 1-3; preferably, the first and second electrodes are formed of a metal,

the alkyl aluminum compound is selected from at least one of trimethyl aluminum, triethyl aluminum, triisobutyl aluminum, trioctyl aluminum, diethyl aluminum monohydrogen, diisobutyl aluminum monohydrogen, diethyl aluminum monochloride, diisobutyl aluminum monochloride, ethyl aluminum sesquichloride and ethyl aluminum dichloride; preferably selected from triethylaluminium and/or triisobutylaluminium.

11. Catalyst system according to any of claims 2 to 10, characterized in that the ratio of the total number of moles of aluminium in the alkylaluminium compound C and the external electron donor a is between 0.5-1 and 50: 1, preferably 1 to 30: 1, more preferably 1 to 20: 1; and/or the presence of a gas in the gas,

in the solid catalyst component B, the content of magnesium in terms of magnesium atom, titanium in terms of titanium atom, halogen in terms of halogen atom, titanium atom is 1.0 to 8.0 wt%, preferably 1.6 to 6.0 wt%; the content of magnesium atoms is preferably 10 to 70 wt%, preferably 15 to 40 wt%; the content of halogen atoms is 20 to 90 wt%, preferably 30 to 85 wt%; the content of the internal electron donor compound is 2-30 wt%, preferably 3-20 wt%; and/or

The molar ratio of aluminium in the aluminium alkyl compound C to titanium in the catalyst system is from 5 to 5000: 1; preferably 20 to 1000: 1; more preferably 50 to 500: 1.

12. a process for the polymerization of olefins comprising contacting one or more olefins with the catalyst system according to any of claims 2-11 to obtain a polymer; preferably, the olefin has the formula CH₂(ii) CHR, R is selected from hydrogen or alkyl of 1 to 6 carbon atoms; more preferably, the olefin is selected from at least one of ethylene, propylene, 1-n-butene, 1-n-pentene, 1-n-hexene, 1-n-octene and 4-methyl-1-pentene; further preferably at least one selected from the group consisting of ethylene, propylene and 1-butene.