CN109678998B - Catalyst component and catalyst system for olefin polymerization, prepolymerized catalyst system and olefin polymerization method - Google Patents
Catalyst component and catalyst system for olefin polymerization, prepolymerized catalyst system and olefin polymerization method Download PDFInfo
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- CN109678998B CN109678998B CN201710996888.2A CN201710996888A CN109678998B CN 109678998 B CN109678998 B CN 109678998B CN 201710996888 A CN201710996888 A CN 201710996888A CN 109678998 B CN109678998 B CN 109678998B
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Abstract
The invention belongs to the field of olefin polymerization, and relates to a catalyst component and a catalyst system for olefin polymerization, a prepolymerization catalyst system and an olefin polymerization method. The catalyst component for olefin polymerization is prepared by a process comprising the steps of; a. contacting a magnesium compound, a compound shown as a general formula (I), an organic alcohol compound and an inert diluent to form a uniform solution, and adding a precipitating agent in the presence of a precipitating agent to precipitate a solid; b. treating the solid precipitated in the step a with a titanium compound, and adding an internal electron donor compound during and/or before the treatment of the solid with the titanium compound to obtain the catalyst component. The catalyst system of the invention has better catalytic activity and orientation performance when used for olefin polymerization, especially propylene polymerization.
Description
Technical Field
The invention relates to the field of olefin polymerization, and more particularly relates to a catalyst component and a catalyst system for olefin polymerization, a pre-polymerized catalyst system obtained by pre-polymerizing the catalyst, and a method for olefin polymerization.
Background
Olefin polymerization catalysts can be divided into three broad categories, namely, traditional Ziegler-Natta catalysts, metallocene catalysts, and non-metallocene catalysts. At present, in the preparation process of the traditional catalyst for Ziegler-Natta propylene polymerization, compounds such as esters, ethers, ketones and the like are generally added as internal electron donors. Wherein the ester compound is mainly dicarboxylic acid ester compound, such as phthalate, malonate, succinate, 1, 3-diol ester, diphenol ester, etc. Early monoester compounds, particularly aromatic monoester compounds such as ethyl benzoate, were used, but the catalysts prepared by using the monoester compounds as internal electron donors have low activity and low isotacticity, and the products need to be atactic-removed, thereby weakening the sight of people.
For the conventional Ziegler-Natta catalysts, polyolefin catalysts are continuously updated with the development of electron donor compounds in the catalysts. Development of the catalyst from the first TiCl3AlCl3/AlEt2Cl system and second generation of TiCl3/AlEt2Cl system, magnesium chloride of the third generation as a carrier, monoester or aromatic dibasic acid ester as an internal electron donor, and TiCl with silane as an external electron donor4·ED·MgCl2/AlR3ED system. The activity and the directional performance of the catalyst are two important indexes for measuring the performance of the catalyst, and the influence of different preparation methods, different internal electron donors and the like on the activity and the directional performance of the catalyst is obvious.Generally, a catalyst with excellent properties should have high polymerization activity while the orientation properties are adjustable.
Patent documents CN103059169A, CN103059171A, CN103059172A, CN103059174A, CN103059173A and the like disclose a catalyst component and a preparation method thereof, wherein a magnesium compound is dissolved in an organic solvent to form a solution, a precipitating agent is added to precipitate a solid, and after solid particles are formed, the catalyst is treated with a phosphorus-containing compound, so that the orientation performance of the catalyst is improved, but the activity of the treated catalyst is obviously reduced, and the activity of the catalyst is low.
Disclosure of Invention
The present invention aims to overcome the defects of the prior art and provide a catalyst component and a catalyst system for olefin polymerization, a pre-polymerization catalyst system and an olefin polymerization method. Repeated experiments show that the addition of a small amount of monoester compound during dissolution can not only improve the particle shape of the catalyst, but also improve the activity of the catalyst, and the catalyst has good orientation capability. The catalyst system has better catalytic activity and orientation performance when being used for olefin polymerization, particularly propylene polymerization, and well realizes the balance of the two performances.
A first aspect of the present invention provides a catalyst component for the polymerization of olefins, prepared by a process comprising the steps of:
a. contacting a magnesium compound, a compound shown as a general formula (I), an organic alcohol compound and an inert diluent to form a uniform solution, and adding a precipitating agent in the presence of a precipitating agent to precipitate a solid;
b. treating the solid precipitated in the step a with a titanium compound, and adding an internal electron donor compound during and/or before the treatment of the solid with the titanium compound to obtain the catalyst component;
in the formula, R1And R2Are identical to each otherOr, different, is a substituted or unsubstituted, straight or branched C1-C20Alkyl radical, C2-C20Alkylene radical, C3-C20Cycloalkyl radical, C6-C20Aryl radical, C7-C20Alkylaryl or C7-C20Aralkyl radical, R1、R2Optionally bonded to form a ring; preferably, R1And R2Identical or different, being a substituted or unsubstituted, linear or branched C1-C10Alkyl radical, C3-C10A cycloalkyl group; further preferably, R1And R2Identical or different, being a substituted or unsubstituted, linear or branched C2-C8An alkyl group.
According to the present invention, particularly preferably, the compounds represented by the general formula (i) include, but are not limited to: at least one of ethyl acetate, ethyl propionate, ethyl n-butyrate, ethyl isobutyrate, ethyl t-butyrate, propyl acetate, propyl propionate, propyl n-butyrate, propyl isobutyrate, and propyl t-butyrate. Most preferred is ethyl acetate.
According to the present invention, the inert diluent may be any of the solvents conventionally used in the art for dissolving the ZN catalyst component, preferably selected from C6-C10Preferably at least one selected from the group consisting of hexane, heptane, octane, decane, benzene, toluene, xylene and derivatives thereof.
According to a preferred embodiment of the present invention, the organic alcohol compound has the general formula R3OH, wherein R3Is a substituted or unsubstituted, straight or branched C1-C20Alkyl radical, C2-C20Alkylene radical, C3-C20Cycloalkyl radical, C6-C20Aryl radical, C7-C20Alkylaryl or C7-C20Aralkyl, preferably selected from linear or branched C2-C10And an alkyl group, further preferably at least one selected from the group consisting of ethanol, butanol and isooctanol.
According to the invention, the precipitation agent may be a metal halide, preferably a titanium halide, more preferably titanium tetrachloride.
According to the present invention, preferably, the precipitation assistant is at least one of organic acid anhydride, organic acid, ester, ketone, aldehyde and ether compound, preferably dicarboxylic ester, and more preferably malonate type compound.
Such elution aids include, but are not limited to: such as: diethyl diisobutyl malonate, diethyl di-n-butylmalonate, diethyl di-tert-butylmalonate, dipropyl diisobutyl malonate, dipropyl di-n-butylmalonate, dipropyl di-tert-butylmalonate, dibutyl diisobutyl malonate, dibutyl di-n-butylmalonate, dibutyl di-tert-butylmalonate, dipentyl diisobutyl malonate, dipentyl di-n-butylmalonate, dipentyl di-tert-butylmalonate, dihexyl di-n-butylmalonate, dihexyl di-tert-butylmalonate, dihexyl di-iso-butylmalonate, diheptyl di-n-butylmalonate, diheptyl di-tert-butylmalonate, dipropyl di-n-pentylmalonate, dipropyl phenylethylmalonate, dipropyl malonate, Dipropyl phenylmethylmalonate, dipropyl phenylpropionate, dipropyl phenylbutylonitrile, dipropyl isobutylphenylmalonate, dipropyl isoamylmalonate, dipropyl phenylpentylglonitrile, dipropyl diphenylmalonate, dipropyl benzylmalonate, dipropyl benzylmethylmalonate, dipropyl benzylpropylmalonate, dipropyl benzylbutylmalonate, dipropyl benzylisobutylmalonate, dipropyl benzylisoamylmalonate, dipropyl benzyln-pentylmalonate, dipropyl dibenzylmalonate, dibutyl phenylethylmalonate, dibutyl phenylmethylmalonate, dibutyl phenylpropyldimalonate, dibutyl n-butylmalonate, dibutyl phenylisobutylmalonate, dibutyl phenylisopentylmalonate, dibutyl phenyln-pentylmalonate, dibutyl diphenylmalonate, Dibutyl benzylethylmalonate, dibutyl benzylmethylpropylmalonate, dibutyl benzylpropylmalonate, dibutyl benzyln-butylmalonate, dibutyl benzylisobutylmalonate, dibutyl benzylisopentylmalonate, dibutyl benzyl-n-pentylmalonate, dibutyl dibenzylmalonate, diamyl phenylethylmalonate, diamyl phenylmethylmalonate, diamyl phenylpropmalonate, diamyl n-butylmalonate, diamyl phenylisobutylmalonate, diamyl phenylisomalonate, diamyl n-pentylmalonate, diamyl phenyln-pentylmalonate, diamyl diphenylmalonate, diamyl benzylethylmalonate, diamyl benzylmethylmalonate, diamyl benzylpropylmalonate, diamyl benzyl n-butylmalonate, diamyl benzylisobutylmalonate, diamyl benzylisopentylmalonate, benzyl n-pentylmalonate, diamyl benzylisoamylmalonate, diamyl benzyln-pentylmalonate, diamyl n-pentylmalonate, diamyl benzyln-pentylmalonate, diamyl isopropylmalonate, dibutyl benzylmalonate, dibutyl n-pentylmalonate, dibutyl benzylisopropylmalonate, dibutyl n-pentylmalonate, benzyl isobutylmalonate, dibutyl, Diamyl dibenzylmalonate, dicyclohexyl phenylethylmalonate, dicyclohexyl phenylmethylmalonate, dicyclohexyl phenylpropylmalonate, dicyclohexyl phenylbutylaluminmalonate, dicyclohexyl phenyleneisophthalate, dicyclohexyl phenylbutylaluminmalonate, dicyclohexyl phenyleneisopropylmalonate, dicyclohexyl phenyln-pentylmalonate, dicyclohexyl diphenylmalonate, dicyclohexyl benzylethylmalonate, dicyclohexyl benzylmethylmalonate, dicyclohexyl benzylpropylmalonate, dicyclohexyl benzyln-butylmalonate, dicyclohexyl benzylisobutylmalonate, dicyclohexyl benzylisoylmalonate, dicyclohexyl benzylmethylisopropylmalonate, dicyclohexyl benzyln-pentylmalonate, dicyclohexyl dibenzylmalonate, diphenyl phenylmethylmalonate, diphenyl phenylpropylmalonate, diphenyl n-butylmalonate, diphenyl phenylisobutylmalonate, diphenyl phenylisoylmalonate, diphenyl phenylmethylisopropylmalonate, diphenyl benzylmalonate, diphenyl phenylmethylisobutylalkylmalonate, diphenyl phenylmethylisopropylmalonate, diphenyl malonate, diphenyl isohexylmalonate, diphenyl malonate, diphenyl propylmalonate, dicyclohexyl phenylbutylmalonate, diphenyl malonate, and/butylmalonate, Phenyl-n-propylmalonic acid diphenyl ester, diphenyl malonic acid diphenyl ester, benzyl ethylmalonic acid diphenyl ester, benzyl methylmalonic acid diphenyl ester, benzyl propylmalonic acid diphenyl ester, benzyl n-butylmalonic acid diphenyl ester, benzyl isobutylmalonic acid diphenyl ester, benzyl isoamylmalonic acid diphenyl ester, benzyl n-pentylmalonic acid diphenyl ester, dibenzylmalonic acid diphenyl ester, fluorenylmethylmalonic acid dicyclohexyl ester, fluorenylpropylmalonic acid dicyclohexyl ester, fluorenyln-butylmalonic acid dicyclohexyl ester, fluorenylisobutylmalonic acid dicyclohexyl ester, fluorenylisoamylmalonic acid dicyclohexyl ester, fluorenyln-pentylmalonic acid dicyclohexyl ester, difluorenylmalonic acid dicyclohexyl ester, allylmethylmalonic acid diphenyl ester, allylpropylmalonic acid diphenyl ester, allyl n-butylmalonic acid diphenyl ester, allyl isobutylmalonic acid diphenyl ester, allyl isoamylmalonic acid diphenyl ester, Allyl n-amyl diphenyl malonate, diallyl diphenyl malonate, allyl methyl dimethyl malonate, allyl propyl dimethyl malonate, allyl n-butyl dimethyl malonate, allyl isobutyl dimethyl malonate, allyl isoamyl dimethyl malonate, allyl n-amyl dimethyl malonate, diallyl dimethyl malonate, allyl methyl diethyl malonate, allyl propyl diethyl malonate, allyl n-butyl diethyl malonate, allyl isobutyl diethyl malonate, allyl isoamyl diethyl malonate, allyl n-amyl diethyl malonate, diallyl diethyl malonate, allyl methyl dipropyl malonate, allyl propyl dipropyl malonate, allyl n-butyl dipropyl malonate, allyl isobutyl malonate, allyl isoamyl dipropyl malonate, allyl isopropyl malonate, isopropyl malonate, Dipropyl allyl n-pentylmalonate, dipropyl diallyl malonate, dibutyl allyl methyl malonate, dibutyl allyl propyl malonate, dibutyl allyl n-butyl malonate, dibutyl allyl isobutyl malonate, dibutyl allyl isoamyl malonate, dibutyl allyl n-pentylmalonate, dibutyl diallyl malonate, dipentyl allyl methyl malonate, dipentyl allyl propyl malonate, dipentyl allyl n-butylmalonate, dipentyl allyl isobutyl malonate, dipentyl allyl isoamyl malonate, dipentyl allyl n-pentylmalonate, dipentyl diallyl malonate, dicyclohexyl allyl methyl malonate, dicyclohexyl allyl propyl malonate, dicyclohexyl allyl n-butylmalonate, dicyclohexyl allyl isobutyl malonate, dicyclohexyl allyl isoamyl malonate, dibutyl allyl propyl malonate, dibutyl malonate, and butyl malonate, The dicyclohexyl allyl n-pentylmalonate and the dicyclohexyl diallylmalonate are preferably selected from the group consisting of diethyl di-isobutylmalonate, diethyl di-n-butylmalonate, diethyl di-t-butylmalonate, dipropyl di-isobutylmalonate, dipropyl di-n-butylmalonate, dipropyl di-t-butylmalonate, diethyl diallylmalonate and dipropyl diallylmalonate.
According to the present invention, the internal electron donor compound may be selected from at least one of a nitrogen-containing compound, an oxygen-containing compound, a phosphorus-containing compound, a sulfur-containing compound, and a silicon-containing compound. The nitrogen-containing compounds, oxygen-containing compounds, phosphorus-containing compounds, sulfur-containing compounds, and silicon-containing compounds that can be used as internal electron donors in the prior art can be used in the present invention. The internal electron donor is preferably selected from oxygen-containing compounds, more preferably selected from mono-or poly-carboxylic acid ester compounds, and even more preferably selected from benzoate compounds. Such as 2, 4-pentanediol dibenzoate, 3, 5-heptanediol dibenzoate, 4-ethyl-3, 5-heptanediol dibenzoate, 3, 5-heptanediol di-p-methylbenzoate, 3, 5-heptanediol di-o-methylbenzoate, 3, 5-heptanediol di-p-chlorobenzoate, 3, 5-heptanediol di-o-chlorobenzoate, 3, 5-heptanediol di-p-methoxybenzoate, 3, 5-heptanediol di-o-methoxybenzoate, 3, 5-heptanediol di-m-methoxybenzoate, 2-methyl-3, 5-heptanediol dibenzoate, 4-methyl-3, 5-heptanediol dibenzoate, 6-methyl-3, 5-heptanediol dibenzoate, 4-ethyl-3, 5-heptanediol dibenzoate, 5-ethyl-3, 5-heptanediol dibenzoate, 4-propyl-3, 5-heptanediol dibenzoate, 4-butyl-3, 5-heptanediol dibenzoate, 2, 4-dimethyl-3, 5-heptanediol dibenzoate, 2, 6-dimethyl-3, 5-heptanediol dibenzoate, 4-dimethyl-3, 5-heptanediol dibenzoate, 6-dimethyl-3, 5-heptanediol dibenzoate, 4-dimethyl-3, 5-heptanediol dibenzoate, 6-dimethyl-3, 5-heptanediol dibenzoate, 2-methyl-4-ethyl-3, 5-heptanediol dibenzoate, 4-methyl-4-ethyl-3, 5-heptanediol dibenzoate, 2-methyl-4-propyl-3, 5-heptanediol dibenzoate, 4-methyl-4-propyl-3, 5-heptanediol dibenzoate, 6-methyl-2, 4-heptanediol di (p-chlorobenzoic acid) ester, 6-methyl-2, 4-heptanediol di (p-methylbenzoic acid) ester, 6-methyl-2, 4-heptanediol di (m-methylbenzoic acid) ester, 2,6, 6-tetramethyl-3, 5-heptanediol dibenzoate, 2,6, 6-heptanediol dibenzoate, 2, 5-heptanediol dibenzoate, 2, 4-heptanediol dibenzoate, 2,6, 6-tetramethyl-3, 5-heptanediol dibenzoate, 2, 4-heptanediol dibenzoate, and mixtures thereof, 4-methyl-3, 5-octanediol dibenzoate, 4-ethyl-3, 5-octanediol dibenzoate, 4-propyl-3, 5-octanediol dibenzoate, 4-butyl-3, 5-octanediol dibenzoate, 4-dimethyl-3, 5-octanediol dibenzoate, 4-methyl-4-ethyl-3, 5-octanediol dibenzoate, 2-methyl-6-ethyl-3, 5-octanediol dibenzoate, 5-methyl-4, 6-nonanediol dibenzoate, 5-ethyl-4, 6-nonanediol dibenzoate, 4-ethyl-3, 5-octanediol dibenzoate, 5-methyl-4, 6-nonanediol dibenzoate, 5-ethyl-4, 6-nonanediol dibenzoate, 4-ethyl-octanediol dibenzoate, 5-methyl-4, 5-octanediol dibenzoate, 5-dimethyl-3, 5-octanediol dibenzoate, 4-dimethyl-3, 4-octanediol dibenzoate, 4-dimethyl-octane-3, 5-octane-diol dibenzoate, 4-dimethyl-octane diol dibenzoate, 4-dimethyl-3, 4-octanediol dibenzoate, 4-dimethyl-3, 4-3, 5-4-octane-diol dibenzoate, 4-dimethyl-4-octane-4-dimethyl-octane-4-octane-5-diol dibenzoate, 4-octane-4-octane-dimethyl-octane-4-octane-4-diol dibenzoate, 4-octane-4-octane-diol dibenzoate, 4-octane-dimethyl-4-octane-diol dibenzoate, 4-2-octane-2, 4-2-octane-dimethyl-octane-2-one, 4-one, and a, 5-propyl-4, 6-nonanediol dibenzoate, 5-butyl-4, 6-nonanediol dibenzoate, 5-dimethyl-4, 6-nonanediol dibenzoate, 5-methyl-4-ethyl-4, 6-nonanediol dibenzoate, 5-phenyl-4, 6-nonanediol dibenzoate, 4, 6-nonanediol dibenzoate and 4-butyl-3, 5-heptanediol dibenzoate, preferably: 2, 4-pentanediol dibenzoate, 3, 5-heptanediol dibenzoate, 4-ethyl-3, 5-heptanediol dibenzoate, 3, 5-heptanediol di-p-methylbenzoate, 3, 5-heptanediol di-o-methylbenzoate, 3, 5-heptanediol di-p-chlorobenzoate, 3, 5-heptanediol di-o-chlorobenzoate, 3, 5-heptanediol di-p-methoxybenzoate, 3, 5-heptanediol di-o-methoxybenzoate, 3, 5-heptanediol di-m-methoxybenzoate, 2-methyl-3, 5-heptanediol dibenzoate, 4-methyl-3, 5-heptanediol dibenzoate, 6-methyl-3, 5-heptanediol dibenzoate, 1, 2-phenylene dibenzoate, 2-heptanediol dibenzoate, 3, 5-diol dibenzoate, 3, 5-heptanediol dibenzoate, 3, 4-xylene dibenzoate, 2-diol dibenzoate, 2, 4-xylene dibenzoate, 2, heptanediol dibenzoate, 3, heptanediol dibenzoate, 4, heptanediol dibenzoate, heptanediol, 4, heptanediol dibenzoate, and the like, 3-methyl-5-tert-butyl-1, 2-diphenylene dibenzoate, 4-methyl-1, 2-diphenylene dibenzoate, etc. The internal electron donor is most preferably selected from substituted or unsubstituted glycol benzoate compounds, such as 3, 5-heptanediol dibenzoate.
According to the present invention, preferably, the magnesium compound is selected from magnesium dihalides, alkoxy magnesium, alkyl magnesium, hydrates or alcoholates of magnesium dihalides and derivatives of magnesium dihalides in which one halogen atom is substituted by hydrocarbyloxy or halohydrocarbyloxy, preferably magnesium dihalides or alcoholates of magnesium dihalides; such as magnesium dichloride, magnesium dibromide, magnesium diiodide, and their alcoholates.
In the invention, the titanium compound can be selected as the general formula TiXm(OR)4-mWherein R is C1-C20X is halogen, and m is more than or equal to 1 and less than or equal to 4. The titanium compounds include but are not limited toLimited to: titanium tetrachloride, titanium tetrabromide, titanium tetraiodide, tetrabutoxytitanium, tetraethoxytitanium, chlorotriethoxytitanium, dichlorodiethoxytitanium, trichloromonoethoxytitanium, preferably titanium tetrachloride.
According to the invention, the inert diluent may be chosen from C6-C10Preferably at least one of the alkanes or aromatic hydrocarbons of (a), selected from hexane, heptane, octane, decane, benzene, toluene, xylene or derivatives thereof.
According to the invention, the compound of the formula (I) is preferably used in an amount of 0.001 to 1 mol, preferably 0.02 to 0.5 mol, per mol of magnesium in the magnesium compound; the dosage of the precipitating agent is 2-40 mol, preferably 4-30 mol; (ii) a The dosage of the organic alcohol compound is 1-15 mol; the dosage of the precipitation aid is 0.001-30 mol, preferably 0.05-15 mol; the using amount of the titanium compound is 3-40 mol, preferably 5-30 mol; the amount of the internal electron donor compound is 0.005 to 15 mol, preferably 0.05 to 5 mol.
A second aspect of the present invention provides a catalyst system for the polymerization of olefins comprising the reaction product of:
1) the above-mentioned catalyst component;
2) an alkyl aluminum compound; preferably, the alkyl aluminium compound has the formula AlR'nX3-nWherein R' is hydrogen or C1-C20X is halogen, n is more than 0 and less than or equal to 3; specifically, the aluminum chloride can be selected from triethyl aluminum, tripropyl aluminum, tri-n-butyl aluminum, triisobutyl aluminum, tri-n-octyl aluminum, triisobutyl aluminum, diethyl aluminum monohydrogen, diisobutyl aluminum monohydrogen, diethyl aluminum monochloride, diisobutyl aluminum monochloride, ethyl aluminum sesquichloride and ethyl aluminum dichloride, and preferably triethyl aluminum and triisobutyl aluminum;
3) optionally, an external electron donor component; preferably, the external electron donor component has the general formula (R)1)kSi(OR2)4-kWhere k is 0-3, R1Selected from halogen, hydrogen atom and C1-C20Alkyl or haloalkyl of, C3-C20Cycloalkyl radical, C6-C20Aryl or amino, R2Is C1-C20Alkyl or haloalkyl of, C3-C20Cycloalkyl radical, C6-C20Aryl or amino.
The "optional external electron donor component" means that the external electron donor compound may be optionally added or not added, as desired. For the application of olefin polymers with high stereoregularity, 3) an external electron donor component is required to be added. The external electron donating components include, but are not limited to: trimethylmethoxysilane, trimethylethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, phenyltriethoxysilane, phenyltrimethoxysilane, vinyltrimethoxysilane, cyclohexylmethyldimethoxysilane, methyl-tert-butyldimethoxysilane, preferably cyclohexylmethyldimethoxysilane, diphenyldimethoxysilane.
The third aspect of the invention provides a prepolymerized catalyst system for olefin polymerization, wherein the prepolymerized catalyst comprises the catalyst component and/or a prepolymer obtained by prepolymerizing the catalyst system and olefin, and the prepolymerization multiple is 0.1-1000 g of olefin polymer per g of solid catalyst component; preferably, the prepolymerization multiple is about 0.2 to 500g of polymer per g of solid catalyst component. The prepolymerization step can be carried out at a temperature of-20 to 80 ℃, preferably 0 to 50 ℃, in a liquid or in a gas phase. The pre-polymerization step may be carried out in-line as part of a continuous polymerization process or separately in a batch operation.
In a fourth aspect, the present invention provides a process for the polymerization of an olefin, preferably said olefin having the formula CH, in the presence of at least one of the above-mentioned catalyst component, the above-mentioned catalyst system and the above-mentioned prepolymerized catalyst system2CHR ', R' is hydrogen, C1-C12Alkyl or C6-C12More preferably the olefin is ethylene or propylene.
The catalyst of the present invention may be directly added to the reactor for use in the polymerization process, or the catalyst may be prepolymerized before being added to the first polymerization reactor to participate in the reaction in the form of a prepolymerized catalyst.
The olefin polymerization reaction of the present invention is carried out according to a known polymerization method, and may be carried out in a liquid phase or a gas phase, or may be carried out by a combination of liquid phase and gas phase polymerization stages. Conventional techniques such as slurry processes, gas phase fluidized beds and the like may be employed wherein the olefin may be selected from ethylene, propylene, 1-butene, 4-methyl-1-pentene and 1-hexene and are particularly suitable for the homopolymerization of propylene or the copolymerization of propylene with other olefins. The following reaction conditions are preferably employed: the polymerization temperature is 0-150 ℃, preferably 60-90 ℃. The polymerization pressure is 0.01 to 10 MPa.
According to the invention, a small amount of monoester compound is added during dissolution, so that the particle type of the catalyst can be improved, the activity of the catalyst can be improved, and the orientation capability of the catalyst is good. Has wide application prospect.
Additional features and advantages of the invention will be set forth in the detailed description which follows.
Detailed Description
The following examples are given for the purpose of illustrating the invention and are not to be construed as limiting the invention.
Test method
Polymer isotactic index II: as determined by heptane extraction (6 hours of heptane boil 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, which was obtained by drying the residue to a constant weight, was defined as the isotactic index.
Melt index MI: measured using a melt index apparatus at 230 ℃ under a pressure of 2.16kg according to ASTM D1238-99 Standard test method for measuring thermoplastic melt flow Rate with an extrusion plastometer.
Polymerization of propylene
A stainless steel reaction vessel having a volume of 5L was sufficiently purged with gaseous propylene, then AlEt32.5mmol and 0.L mmol of methylcyclohexyldimethoxysilane (CHMMS) were added thereto, 10mg of the following catalyst component and 1.2L of hydrogen (standard state) were further added thereto, and 2.3L of liquid propylene was introduced thereinto, and the temperature was raised to 70 ℃ and maintained at this temperature for 1 hour. And (5) cooling and decompressing to obtain the PP powder. The data are shown in table 1.
Example 1
Under the protection of nitrogen, adding 4.8g of anhydrous magnesium chloride, 19.5g of isooctanol, 0.5mL of ethyl acetate and 19.5g of decane solvent into a 500mL reactor provided with a stirrer, heating to 130 ℃, reacting for 1.5 hours until the magnesium chloride is completely dissolved, adding 8mmol of diethyl diallyl malonate, and continuously maintaining the temperature at 130 ℃ for reacting for 1 hour to obtain an alcohol compound; the alcohol hydrate was cooled to room temperature. Under the protection of nitrogen, the alcohol compound is added into 120ml titanium tetrachloride solution which is precooled to minus 22 ℃, the temperature is slowly increased to 100 ℃, and solid is gradually separated out in the process of temperature increase. Then, 10mmol of 3, 5-heptanediol dibenzoate compound was added to the solid, the mixture was heated to 110 ℃ and maintained for 2 hours, and then filtered while it was still hot, 120ml of titanium tetrachloride was added, the mixture was heated to 110 ℃ and reacted for 1 hour, and then filtered. The filtered solid particles were washed four times with anhydrous hexane and dried to obtain a solid catalyst.
Example 2
The procedure is as in example 1, except that 0.8mL of ethyl acetate is used instead of 0.5mL of ethyl acetate.
Example 3
The procedure is as in example 1, except that 0.2mL of ethyl acetate is used instead of 0.5mL of ethyl acetate.
Example 4
The process was the same as in example 1 except that propyl acetate was used instead of ethyl acetate.
Example 5
The process was the same as in example 1 except that propyl propionate was used instead of ethyl acetate.
Example 6
The procedure is as in example 1, except that 3-methyl-5-tert-butyl-1, 2-diphenylenedibenzoate is used instead of 3, 5-heptanediol dibenzoate.
Comparative example 1
Under the protection of nitrogen, adding 4.8g of anhydrous magnesium chloride, 19.5g of isooctanol and 19.5g of decane solvent into a 500ml reactor provided with a stirrer, heating to 130 ℃, reacting for 1.5 hours until the magnesium chloride is completely dissolved, adding 8mmol of diethyl diisobutyl malonate, and continuously maintaining the temperature at 130 ℃ for reacting for 1 hour to obtain an alcohol compound; the alcohol hydrate was cooled to room temperature. Under the protection of nitrogen, the alcohol compound is added into 120ml titanium tetrachloride solution which is precooled to minus 22 ℃, the temperature is slowly increased to 100 ℃, and solid is gradually separated out in the process of temperature increase. Then, 10mmol of 3, 5-heptanediol dibenzoate compound was added to the solid, the mixture was heated to 110 ℃ and maintained for 2 hours, and then filtered while it was still hot, 120ml of titanium tetrachloride was added, the mixture was heated to 110 ℃ and reacted for 1 hour, and then filtered. The filtered solid particles were washed four times with anhydrous hexane and dried to obtain a solid catalyst.
Comparative example 2
Under the protection of nitrogen, adding 4.8g of anhydrous magnesium chloride, 19.5g of isooctanol and 19.5g of decane solvent into a 500ml reactor provided with a stirrer, heating to 130 ℃, reacting for 1.5 hours until the magnesium chloride is completely dissolved, adding 8mmol of diethyl diallyl malonate, and continuously maintaining the temperature at 130 ℃ for reacting for 1 hour to obtain an alcohol compound; the alcohol hydrate was cooled to room temperature. Under the protection of nitrogen, the alcohol compound is added into 120ml titanium tetrachloride solution which is precooled to minus 22 ℃, the temperature is slowly increased to 100 ℃, and solid is gradually separated out in the process of temperature increase. Then, 10mmol of 3-methyl-5-tert-butyl-1, 2-diphenylene dibenzoate compound was added to the solid, the mixture was heated to 110 ℃ and maintained for 2 hours, and then filtered while it was still hot, 120ml of titanium tetrachloride was added thereto, the mixture was heated to 110 ℃ and reacted for 1 hour, followed by filtration. The filtered solid particles were washed four times with anhydrous hexane and dried to obtain a solid catalyst.
TABLE 1
As can be seen from the data in Table 1, the catalyst of the present invention has better catalytic activity and better catalyst orientation ability than the prior art (comparative examples 1-2).
Having described embodiments of the present invention, the foregoing description is intended to be exemplary, not exhaustive, and not limited to the embodiments disclosed. Many modifications and variations will be apparent to those of ordinary skill in the art without departing from the scope and spirit of the described embodiments.
Claims (27)
1. A catalyst component for the polymerization of olefins prepared by a process comprising the steps of:
a. contacting a magnesium compound, a compound shown as a general formula (I), an organic alcohol compound and an inert diluent to form a uniform solution, and adding a precipitating agent in the presence of a precipitating agent to precipitate a solid;
b. treating the solid precipitated in the step a with a titanium compound, and adding an internal electron donor compound during and/or before the treatment of the solid with the titanium compound to obtain the catalyst component;
in the formula, R1And R2Identical or different, being unsubstituted, linear or branched C1-C8An alkyl group;
the precipitation aid is a malonate compound.
2. The catalyst component according to claim 1 in which the organic alcohol compound has the general formula R3OH, wherein R3Is a substituted or unsubstituted, straight or branched C1-C20Alkyl radical, C2-C20Alkylene radical, C3-C20Cycloalkyl radical, C6-C20Aryl radical, C7-C20Alkylaryl or C7-C20An aralkyl group.
3. The catalyst component according to claim 2 in which R is3Selected from straight or branched C2-C10An alkyl group.
4. The catalyst component according to claim 3 in which the organic alcohol compound is selected from at least one of ethanol, butanol and isooctanol.
5. The catalyst component according to claim 1 in which the precipitating agent is a metal halide.
6. The catalyst component according to claim 5 in which the precipitation agent is a titanium halide.
7. The catalyst component according to claim 6 in which the precipitating agent is titanium tetrachloride.
8. The catalyst component according to claim 1 in which the internal electron donor compound is selected from at least one of nitrogen containing compounds, oxygen containing compounds, phosphorous containing compounds, sulfur containing compounds and silicon containing compounds.
9. The catalyst component according to claim 8 in which the internal electron donor compound is selected from oxygen containing compounds.
10. The catalyst component according to claim 9 in which the internal electron donor compound is selected from mono or polycarboxylic acid ester compounds.
11. The catalyst component according to claim 10 in which the internal electron donor compound is selected from the benzoate compounds.
12. The catalyst component according to claim 11 in which the internal electron donor compound is selected from substituted or unsubstituted glycol benzoates.
13. The catalyst component according to claim 1 in which the magnesium compound is selected from magnesium dihalides, magnesium alkoxides, magnesium alkyls, hydrates or alcoholates of magnesium dihalides and derivatives of magnesium dihalides in which one of the halogen atoms is substituted by hydrocarbyloxy or halohydrocarbyloxy;
the general formula of the titanium compound is TiXm(OR)4-mWherein R is C1-C20X is halogen, and m is more than or equal to 1 and less than or equal to 4.
14. The catalyst component according to claim 13 in which the magnesium compound is a magnesium dihalide or an alcoholate of a magnesium dihalide.
15. The catalyst component according to any of claims 1 to 14 in which the compound of formula (i) is used in an amount of 0.001 to 1 mole per mole of magnesium compound; the dosage of the precipitating agent is 2-40 mol; the dosage of the organic alcohol compound is 1-15 mol; the dosage of the precipitation aid is 0.001-30 mol; the using amount of the titanium compound is 3-40 mol; the dosage of the internal electron donor compound is 0.005-15 mol.
16. The catalyst component according to claim 15 in which the compound of formula (I) is used in an amount of 0.02 to 0.5 mole per mole of magnesium compound.
17. The catalyst component according to claim 15 in which the amount of precipitating agent is 4 to 30 moles per mole of magnesium compound.
18. The catalyst component according to claim 15 in which the precipitation aid is used in an amount of 0.05 to 15 moles per mole of magnesium in the magnesium compound.
19. The catalyst component according to claim 15 in which the titanium compound is used in an amount of 5 to 30 moles per mole of magnesium in the magnesium compound.
20. The catalyst component according to claim 15 in which the internal electron donor compound is used in an amount of 0.05 to 5 moles per mole of magnesium in the magnesium compound.
21. A catalyst system for the polymerization of olefins comprising the reaction product of:
1) the catalyst component of any one of claims 1 to 20;
2) an alkyl aluminum compound;
3) optionally, an external electron donor component.
22. The catalyst system according to claim 21, wherein the alkylaluminum compound has the general formula AlR'nX3-nWherein R' is C1-C20X is halogen, n is more than 0 and less than or equal to 3.
23. The catalyst system of claim 21, wherein the external electron donor component has the general formula (R)1)kSi(OR2)4-kWhere k is 0-3, R1Selected from halogen, hydrogen atom and C1-C20Alkyl or haloalkyl of, C3-C20Cycloalkyl radical, C6-C20Aryl radical, R2Is C1-C20Alkyl or haloalkyl of, C3-C20Cycloalkyl radical, C6-C20And (4) an aryl group.
24. A prepolymerized catalyst system for the polymerization of olefins comprising the catalyst component according to any of claims 1 to 20 and/or a prepolymer obtained by prepolymerizing the catalyst system according to any of claims 21 to 23 with olefins, the prepolymerization factor being from 0.1 to 1000g of olefin polymer per g of solid catalyst component.
25. A process for the polymerization of olefins carried out in the presence of at least one of the catalyst component of any of claims 1 to 20, the catalyst system of any of claims 21 to 23 and the prepolymerized catalyst system of claim 24.
26. The process for the polymerization of olefins according to claim 25, wherein the olefin has the general formula CH2= CHR ', R' is hydrogen, C1-C12Alkyl or C6-C12Aryl group of (1).
27. The olefin polymerization process of claim 26, wherein the olefin is ethylene or propylene.
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| WO2011028178A1 (en) * | 2009-09-07 | 2011-03-10 | Irpc Public Company Limited | Highly active, morphologically-controled ziegler-natta polyethylene catalyst and method of preparing the same |
| CN103012626A (en) * | 2011-09-23 | 2013-04-03 | 中国石油化工股份有限公司 | Olefin polymerization catalyst ingredient, preparation method of the olefin polymerization catalyst ingredient, catalyst system, use of the catalyst system, and olefin polymerization method |
| CN104558292A (en) * | 2013-10-28 | 2015-04-29 | 中国石油化工股份有限公司 | Preparation method of catalyst for olefin polymerization |
| CN105566523A (en) * | 2014-10-10 | 2016-05-11 | 中国石油化工股份有限公司 | Catalyst component used for ethylene homopolymerization or copolymerization reaction, and catalyst thereof |
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| WO2011028178A1 (en) * | 2009-09-07 | 2011-03-10 | Irpc Public Company Limited | Highly active, morphologically-controled ziegler-natta polyethylene catalyst and method of preparing the same |
| CN103012626A (en) * | 2011-09-23 | 2013-04-03 | 中国石油化工股份有限公司 | Olefin polymerization catalyst ingredient, preparation method of the olefin polymerization catalyst ingredient, catalyst system, use of the catalyst system, and olefin polymerization method |
| CN104558292A (en) * | 2013-10-28 | 2015-04-29 | 中国石油化工股份有限公司 | Preparation method of catalyst for olefin polymerization |
| CN105566523A (en) * | 2014-10-10 | 2016-05-11 | 中国石油化工股份有限公司 | Catalyst component used for ethylene homopolymerization or copolymerization reaction, and catalyst thereof |
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