CN102453126A - Catalyst component for olefin polymerization, preparation method and application thereof - Google Patents
Catalyst component for olefin polymerization, preparation method and application thereof Download PDFInfo
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- CN102453126A CN102453126A CN2010105113101A CN201010511310A CN102453126A CN 102453126 A CN102453126 A CN 102453126A CN 2010105113101 A CN2010105113101 A CN 2010105113101A CN 201010511310 A CN201010511310 A CN 201010511310A CN 102453126 A CN102453126 A CN 102453126A
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Abstract
The present invention provides a catalyst component for olefin polymerization, a preparation method and an application thereof. The catalyst component is a reaction product, which contains at least an organic magnesium compound, at least a liquid titanium-containing compound, at least a hydroxyl-containing compound, at least a chlorine-containing silicone compound, and at least a modified additive, wherein the modified additive is a polybutadiene-polyethylene oxide block copolymer. The prepared catalyst has good hydrogen regulation performance, and good particle morphology and distribution, such that the catalyst is easily used on the gas phase, the slurry, and other polymerization process devices.
Description
Technical field
The present invention relates to a kind of catalyst component and catalyzer thereof that is used for olefinic polymerization or copolymerization, and the preparation method of this catalyst component and purposes.
Technical background
Over nearly more than 20 years; Follow the development of olefin polymetiation process; Also got significant progress with the catalyzer that polymerization technique matches, wherein effective catalyst relies on its good polymerization and sophisticated utilisation technology in the polyolefin catalyst field, still to occupy an important position.Through exploratory development for many years, Mg-Ti be the preparation method of effective catalyst also by polishing altogether, the suspension pickling process has developed into chemical reaction method.In chemical reaction method; Many patents of invention relate to chemical feedstockss such as adopting organo-metallic magnesium compound, chlorizating agent and transition metal titanium compound; Use this type reactant to prepare the catalyzer of number of different types, they are disclosed in Chinese patent CN1158136, CN1795213 and U.S. Pat 4508843,4921920 and 5124296.In such Mg-Ti catalyzer, it is to be difficult to control forming step that a fatal shortcoming is all arranged, thereby is difficult to control prepared catalyst particulate form; Recent development is to comprise in the wind prose style free from parallelism system of magnesium/titanium compound at catalyst precursor, adds the material of some similar emulsifying agents, makes it to form emulsion; And then reaction precipitation goes out granules of catalyst, can improve the particle form of gained catalyzer, like the PFPE that in the EP0258089A of Montedison, adopts; In Chinese patent CN1537118A, mention the employing PFO; These method forming step are complicated, are difficult to control, and gained granules of catalyst form is also wayward; And the material expensive that is adopted, be difficult to obtain.
Although done number of research projects,, still need some new or improved methods for preparing the more ZN catalyzer of high performance requirements in the Ziegler-Natta catalyst field.
The inventor selects suitable property-modifying additive through experiment discovery repeatedly, just can make process for synthetic catalyst simple; And it is better to obtain form; Like sphere, the granules of catalyst of narrow size-grade distribution has advantages of high catalytic activity and hydrogen response simultaneously.
Summary of the invention
One of the object of the invention is the solid particulate for preparing Ziegler-Natta catalyst with a kind of controlled mode, thereby it is better to obtain form, and like sphere, the granules of catalyst of narrow size-grade distribution has advantages of high catalytic activity and hydrogen response simultaneously.
Two of the object of the invention is to provide the olefin polymerization catalysis that adopts the inventive method to obtain.
The invention provides a kind of catalyst component that is used for olefinic polymerization; It is to comprise at least a organo-magnesium compound; At least a titanium-containing compound, the reaction product of at least a hydroxyl compounds and at least a chloride silicoorganic compound and at least a property-modifying additive.The catalyzer of preparation removes has good hydrogen regulation performance, also has good particle form and distribution simultaneously, thereby more helps the use of catalyzer on polymerization technique devices such as gas phase, slurry.
A kind of catalyst component that is used for olefinic polymerization of the present invention; It is to comprise at least a organo-magnesium compound; At least a liquid titanium-containing compound, the reaction product of at least a hydroxyl compounds and at least a chloride silicoorganic compound and at least a property-modifying additive; Wherein:
(1) organo-magnesium compound is by general formula (I) MgR
1 nCl
2-nShown in, R in the formula
1Be C
2～C
20Alkyl, optional be saturated or undersaturated straight chain, side chain or closed chain, 0＜n≤2;
(2) titanium-containing compound is by logical formula II Ti (OR
2)
nCl
4-nShown in, R in the formula
2Be C
2～C
20Alkyl, optional be saturated or undersaturated straight chain, side chain or closed chain, 0≤n≤4;
(3) the hydroxyl compounds is like logical formula III HOR
3Shown in, R is C in the formula
2～C
20Alkyl, optional be saturated or undersaturated straight chain, side chain or closed chain.
(4) chloride silicoorganic compound are like logical formula IV SiR
nCl
4-nShown in, R is C in its Chinese style
2～C
20Alkyl or alkoxyl group, 0≤n in the general formula＜4.
(5) property-modifying additive is a polybutadiene block polyethylene oxide base polymer; Comprise diblock and three blocks and verivate thereof etc.; Randomly for linear, that side chain is arranged or star etc. other form; In described polyhutadiene poly-ethylene oxide block analog copolymer, the content of polyhutadiene is 3-97% (wt%).
Described organo-magnesium compound such as general formula (I) MgR
1 nCl
2-nShown in, R is C in the formula
2～C
20Alkyl, can be saturated or undersaturated straight chain, side chain or closed chain, 0＜n≤2.Concrete compound such as MgCl
2, MgEtCl, MgBu
2, the preferred dibutylmagnesium of the organo-magnesium compound that uses in the reaction, diisobutyl magnesium, dioctyl magnesium, fourth octyl group magnesium, ethyl-magnesium-chloride, butyl magnesium chloride are medium.
Described liquid titanium-containing compound is like logical formula II Ti (OR
2)
nCl
4-nShown in, R is C in the formula
2～C
20Alkyl, can be saturated or undersaturated straight chain, side chain or closed chain, 0≤n≤4.The preferred tetravalent titanium compound that uses, because they are in a liquid state usually at normal temperatures, and also also fine with the consistency of some solvents under normal conditions.The concrete titanium compound that uses preferably uses tetravalent titanium compound and their mixture in the reaction, and wherein titanium tetrachloride, tetraethyl titanate and tetrabutyl titanate are the most commonly used.
Described hydroxyl compounds is like logical formula III HOR
3Shown in, R is C in the formula
2～C
20Alkyl, can be saturated or undersaturated straight chain, side chain or closed chain.The hydroxyl compounds is Fatty Alcohol(C12-C14 and C12-C18) or aromatic alcohol, preferred propyl carbinol, n-hexyl alcohol, isooctyl alcohol, phenylcarbinol, phenylethyl alcohol and composition thereof etc.
Described chloride silicoorganic compound are like logical formula IV SiR
nCl
4-nShown in, R is C in its Chinese style
2～C
20Alkyl or alkoxyl group; 0≤n in the general formula＜4; Concrete chloride silicoorganic compound comprise trichlorophenyl silane, trichloromethyl silane, trichloroethyl silane, trichlorine octyl group silane, trichlorine methoxy silane, trichlorine Ethoxysilane, trichlorine butoxy silane, dichloro dimethoxy silane, dichloro diethoxy silane, silicon tetrachloride, and wherein trichloromethyl silane, trichloroethyl silane, trichlorine methoxy silane, trichlorine Ethoxysilane and silicon tetrachloride are preferred.
Described property-modifying additive is polybutadiene block polyethylene oxide (PB-b-POE) base polymer; Comprise diblock and three blocks (PB-b-POE-b-PB, POE-b-PB-b-POE) and verivate thereof etc., can be linear, side chain arranged or star etc. other form.In described polyhutadiene poly-ethylene oxide block analog copolymer, the content of polyhutadiene is 3-97% (wt), preferred 10-90% (wt).
Catalyst component of the present invention preferably adopts the following step to prepare:
(1) organo-magnesium compound and hydroxyl compounds are reacted, obtain clear solution;
(2) property-modifying additive is dispersed in C
4～C
20In alkane or the aromatic solvent, formation solution reacts with the clear solution that chloride silicoorganic compound and step (1) obtain again, obtains mixed solution;
(3) titanium-containing compound is joined in the mixed solution that step (2) obtains, obtain catalyst component.
In the preparation process of catalyst component of the present invention, the ratio between the each component is that in every mole of general formula (I) compound, logical formula II compound is controlled at 0.01～10 mole, preferred 0.05～5 mole; Logical formula III compound is controlled at 0.1～20 mole, preferred 0.2～10 mole; Logical formula IV compound amount is controlled at 0.05～50 mole, preferred 0.1～20 mole; The concentration of property-modifying additive in reaction system is controlled at 0.001～100 grams per liter, preferred 0.01～50 grams per liter.
In the first step of preparation catalyzer, the temperature of reaction of magnesium compound and alcohols material is typically chosen in carries out comparatively favourablely under the higher relatively temperature, and preferably below the boiling temperature of reactant, temperature is not higher than 90 ℃ usually, generally is not higher than 70 ℃.The time of reaction is depended on the character and the operational condition of reactant, and required time is generally at 5 minutes to 2 hours, preferred 10 minutes to 1 hour.After treating the reaction of magnesium compound and alcohols material; The solution that forms can mix use with inert diluent; Inert diluent is selected from aliphatic hydrocarbon usually, for example Trimethylmethane, pentane, hexane, heptane or hexanaphthene and composition thereof, and general hexane or heptane are proper inert solvents.
In second step of preparation catalyzer; With the reaction solution thorough mixing that obtains in a certain amount of property-modifying additive hexane solution for preparing in advance and the first step; According to the kind and the different in kind of property-modifying additive, its hexane solution configuration concentration is controlled at 0.1～100 grams per liter, preferred 1～50 grams per liter; The amount that adds is so that the concentration of property-modifying additive in reaction system is controlled at 0.001～100 grams per liter, preferred 0.01～50 grams per liter.Mixing temperature generally will be lower than the boiling temperature of system, for simplicity, is typically chosen between 0～90 ℃, between preferred 10～50 ℃.Both mixing times are general selects 0.5 minute to 5 hours, preferred 10 minutes to 1 hour.
In the 3rd step of Preparation of Catalyst; Accomplish the uniform mixing of all materials at a certain temperature rapidly, the solution system that at first preceding two steps is obtained is reduced to certain temperature, and solution still keeps clear under this temperature; Be unlikely to become turbid or precipitate; Temperature can be controlled between-90～30 ℃, preferably between-70～0 ℃, will lead to formula IV compound and logical formula II compound then and progressively slowly add successively; In reinforced process, fully stir the thorough mixing that is beneficial to various materials usually, feed rate is selected to be as the criterion not cause that significant reaction or system obviously heat up usually.Behind the thorough mixing, can adopt any known suitable method to heat up, as slowly, progressively, rapidly or temperature programming; Different temperature-rising methods can obtain the totally different catalyzer of performance characteristics, and in temperature-rise period, system can change muddiness into by clarification; Separate out deposition, in this precipitin reaction step, the reaction times of settling step should be long enough to obtain deposition completely; Reaction times can be lasted 1 minute to 10 hours, preferred 3 minutes～5 hours.
Experiment finds, after settling step, reacting for some time at a certain temperature, to carry out maturation process more favourable to the particle shape of catalyzer, and it can improve the intensity of catalyst particle, thereby reduces the particle fragmentation phenomenon of catalyzer in polymerization process.The temperature of maturation process generally is equal to or higher than the outlet temperature of precipitin reaction, and the time of slaking reaction can be controlled at 0.5～10 hour, preferred 1～5 hour.
After carrying out maturation process; Generally to wash; So that remove the by product that forms in excessive reactant and the preparation process, any inert solvent all can be used for this washing step, for example can select Trimethylmethane, pentane, hexane, heptane, hexanaphthene, toluene or various aromatic hydrocarbons and composition thereof etc.; Usually select in the experiment to use the hexane thorough washing own again with after twice of the toluene wash.After washing, carry out drying under the catalyst suspension nitrogen protection, to obtain catalyst fines.
In addition, the invention still further relates to a kind of catalyzer that is used for olefinic polymerization or copolymerization, it comprises the reaction product of following component:
(a) catalyst component of the invention described above;
(b) at least a general formula is AlR " '
3Organo-aluminium compound, R in the formula " ' be C identical or inequality
1-8Alkyl, one of them or two alkyl can be replaced by chlorine.Can select for use one or more aluminum alkyls to mix use, preferred AlEt
3, Al (iso-Bu)
3, Al (n-C
6H
13)
3, Al (n-C
8H
17)
3, AlEt
2Cl etc.
The catalyzer that the present invention relates to can use according to the well-known way of this area olefinic polymerization Ziegler-Natta catalyst; As using, can also said catalyzer be mixed use with one or more Ziegler-Natta catalysts or non-Ziegler-Natta catalyst with another kind of promotor or electron donor.
Catalyst component of the present invention is applicable to various any alkene that can carry out the polycoordination reaction; Comprise a kind of equal polymerization of alkene or the copolymerization of multiple alkene; Terminal olefins such as optimal ethylene, propylene, butylene in the alkene, or the mixture of ethene, propylene, butylene and one or more terminal olefins.Comonomer is a C2-C12 alkene preferably, and preferred C4-C10 alkene is like 1-butylene, iso-butylene, 1-amylene, 1-hexene, 1-heptene, 1-octene, 1-nonene, 1-decene and 4-methylpentene-1; Diene such as divinyl; 1,4-hexadiene and 1,7-octadiene; Cyclenes such as norbornylene, and their any mixture.
Catalyzer of the present invention can adopt conventional polymerization technique to carry out polyreaction in one or more polymerization reactors, can be gas phase, slurry or bulk polymerization, and polyreaction can be intermittence or continuous polymerization process.
To slurry or bulk reaction device, temperature of reaction is generally at 40-130 ℃, and preferred 60-110 ℃, reactor pressure is generally at 0.2-8MPa, preferred 1-6MPa, and the residence time is generally at 0.2-6 hour, preferred 0.5-3 hour.The general boiling point of selecting uses as thinner at the aliphatic hydrocarbon of-70-100 ℃ scope, and if desired, polyreaction can be carried out under super critical condition.
For Gas-phase reactor, temperature of reaction is generally at 60-130 ℃, and preferred 70-110 ℃, reactor pressure is generally at 0.5-4MPa, preferred 1-3MPa, and the residence time is generally at 0.5-10 hour, preferred 1-8 hour.If desired, select suitable aliphatic hydrocarbon to use as thinner, polyreaction can be carried out under the frozen state condition.
Catalyst levels generally depends on character, type of reactor and the operational condition of catalyzer and to the polymerisate performance demands, can use the conventional catalyst consumption.
Adopt catalyzer according to the invention; Can obtain to have the catalystsystem of good form; And catalyzer has advantages of high catalytic activity and better hydrogen regulation sensitivity; The polymerisate form can be duplicated the particle form of catalyzer preferably, and promptly so-called " print effect ", so this catalyzer has excellent comprehensive performances.
Embodiment
Testing method:
1, the size-grade distribution of carrier and catalyzer: MASTERSIZE particles distribution instrument, normal hexane be as dispersion agent, useful range 0.02～2000 μ m.
2, the relative weight per-cent of metal (mainly being titanium, magnesium) in the catalyst system: plasma emission spectrum (ICP).
3, the pattern of catalyzer and polymkeric substance: ESEM (SEM).
4, the mensuration of melting index: ASTM-D 1238.
5, the mensuration of tap density: DIN-53194.
Embodiment given below is for the present invention is described, rather than limits the invention.
Embodiment 1:
Get dibutylmagnesium hexane solution (1M) and the 1.0ml isooctyl alcohol of 30ml hexane, 3.15ml successively, be warming up to 50 ℃ and keep stirring reaction half a hour, obtain clear solution; Add polybutadiene block polyethylene oxide copolymer (polybutadiene content 75wt%) hexane solution (10g/L) 2ml then; Be cooled to-10 ℃, add 0.36 milliliter of silicon tetrachloride and 0.35ml titanium tetrachloride successively, add material after; Be rapidly heated to 50 ℃ in 10 minutes, and keep reaction 2 hours.The catalyst suspension temperature is reduced to room temperature, leave standstill, sedimentation, with hexane wash three times, the consumption of each hexane is 50 milliliters, after washing is accomplished, dry the mobile powder of brown solid, its median size is 37.4 microns.
Ultimate analysis (ICP): Ti:10.06% (weight), Mg:19.29% (weight).
Vinyl polymerization is estimated A: 1L hexane, 1mmol triethyl aluminum and a certain amount of catalyzer are joined in the 2L stainless steel stirring tank, then temperature is brought up to 85 ℃, the hydrogen of disposable adding 0.5MPa; With ethene the total pressure of system is maintained 1.03MPa then and carry out polyreaction, react after 2 hours, stop to add ethene; Cooling; Pressure release, polyethylene powder is weighed, and calculates activity of such catalysts; The tap density of test polyethylene powder and the melting index under the 2.16Kg load, the result is as shown in table 1.
Vinyl polymerization is estimated B: 1L hexane, 1mmol triethyl aluminum and a certain amount of catalyzer are joined in the 2L stainless steel stirring tank, then temperature is brought up to 85 ℃, the hydrogen of disposable adding 0.18MPa; With ethene the total pressure of system is maintained 1.03MPa then and carry out polyreaction, react after 2 hours, stop to add ethene; Cooling; Pressure release, polyethylene powder is weighed, and calculates activity of such catalysts; The tap density of test polyethylene powder and the melting index under the 2.16Kg load, the result is as shown in table 1.
Embodiment 2
In 10 minutes in the catalyst preparation process, be rapidly heated to 50 ℃, change temperature programming to 50 in 120 minutes ℃ into, other conditions are with embodiment 1, and its median size is 43.7 microns.
Ultimate analysis (ICP): Ti:6.24% (weight), Mg:13.55% (weight).
The ethene slurry polymerization appreciation condition of catalyzer is with embodiment 1, and polymerization result is seen table 1.
Embodiment 3
Change the 1.0ml isooctyl alcohol in the catalyst preparation process into the 0.6ml propyl carbinol; Change polybutadiene block polyethylene oxide copolymer (polybutadiene content 75wt%) hexane solution (10g/L) 2ml into polybutadiene block polyethylene oxide copolymer (polybutadiene content 75wt%) hexane solution (10g/L) 10ml; Other conditions are with embodiment 1, and its median size is 18.7 microns.
Ultimate analysis (ICP): Ti:11.54% (weight), Mg:23.69% (weight).
The ethene slurry polymerization appreciation condition of catalyzer is with embodiment 1, and polymerization result is seen table 1.
Comparative Examples 1
Adding polybutadiene block polyethylene oxide copolymer (polybutadiene content 75wt%) hexane solution (10g/L) 2ml in the catalyst preparation process is removed; Other conditions are with embodiment 1; Its median size is 79.46 microns, and size distribution is the multimodal distribution than broad.
Ultimate analysis (ICP): Ti:9.73% (weight), Mg:21.06% (weight).
The ethene slurry polymerization appreciation condition of catalyzer is with embodiment 1, and polymerization result is seen table 1.
Table 1
Can find out from the experimental data of table 1 embodiment and Comparative Examples; In the Preparation of catalysts process, use polybutadiene block polyethylene oxide analog copolymer; The catalyzer that obtains and the particle form of polymkeric substance are good; Narrow particle size distribution, (BD) is higher for the tap density of polymer resin, the catalyzer high comprehensive performance.
Claims (16)
1. catalyst component that is used for olefinic polymerization; It is to comprise at least a organo-magnesium compound; At least a liquid titanium-containing compound, the reaction product of at least a hydroxyl compounds and at least a chloride silicoorganic compound and at least a property-modifying additive; Wherein:
(1) organo-magnesium compound is by general formula (I) MgR
1 nCl
2-nShown in, R in the formula
1Be C
2～C
20Alkyl, optional be saturated or undersaturated straight chain, side chain or closed chain, 0＜n≤2;
(2) titanium-containing compound is by logical formula II Ti (OR
2)
nCl
4-nShown in, R in the formula
2Be C
2～C
20Alkyl, optional be saturated or undersaturated straight chain, side chain or closed chain, 0≤n≤4;
(3) the hydroxyl compounds is like logical formula III HOR
3Shown in, R is C in the formula
2～C
20Alkyl, optional be saturated or undersaturated straight chain, side chain or closed chain;
(4) chloride silicoorganic compound are like logical formula IV SiR
nCl
4-nShown in, R is C in its Chinese style
2～C
20Alkyl or alkoxyl group, 0≤n in the general formula＜4;
(5) property-modifying additive is a polybutadiene block polyethylene oxide base polymer; Comprise diblock and three blocks and verivate thereof; Randomly be linear, form that side chain is arranged or star; In described polyhutadiene poly-ethylene oxide block analog copolymer, the content of polyhutadiene is 3-97% (wt%).
2. the catalyst component that is used for olefinic polymerization according to claim 1, in the wherein said organo-magnesium compound general formula (I), R
1Be C
2～C
20Alkyl.
3. the catalyst component that is used for olefinic polymerization according to claim 2, wherein said organo-magnesium compound are selected from least a in dibutylmagnesium, diisobutyl magnesium, dioctyl magnesium, fourth octyl group magnesium, ethyl-magnesium-chloride and the butyl magnesium chloride.
4. the allylic olefin polymeric catalyst component that is used for according to claim 1, wherein said titanium-containing compound is selected from tetravalent titanium compound.
5. the allylic olefin polymeric catalyst component that is used for according to claim 4, wherein said titanium-containing compound are selected from least a in titanium tetrachloride, tetraethyl titanate and the tetrabutyl titanate.
6. the allylic olefin polymeric catalyst component that is used for according to claim 3, wherein said titanium-containing compound is a titanium tetrachloride.
7. the catalyst component that is used for olefinic polymerization according to claim 1, wherein said hydroxyl compounds are selected from least a in propyl carbinol, n-hexyl alcohol, isooctyl alcohol, phenylcarbinol and the phenylethyl alcohol.
8. the catalyst component that is used for olefinic polymerization according to claim 1, wherein said chloride silicoorganic compound are selected from least a in trichlorophenyl silane, trichloromethyl silane, trichloroethyl silane, trichlorine octyl group silane, trichlorine methoxy silane, trichlorine Ethoxysilane, trichlorine butoxy silane, dichloro dimethoxy silane, dichloro diethoxy silane, the silicon tetrachloride.
9. the catalyst component that is used for olefinic polymerization according to claim 8, wherein said chloride silicoorganic compound are selected from least a in trichloromethyl silane, trichloroethyl silane, trichlorine methoxy silane, the silicon tetrachloride.
10. the catalyst component that is used for olefinic polymerization according to claim 1, the content of polyhutadiene is 10-90% (wt%) in the wherein said polybutadiene block polyethylene oxide base polymer.
11. the preparation method of the said catalyst component of one of claim 1-10 comprises the steps:
(1) organo-magnesium compound and hydroxyl compounds are reacted, obtain clear solution;
(2) property-modifying additive is dispersed in C
4～C
20In alkane or the aromatic solvent, formation solution reacts with the clear solution that chloride silicoorganic compound and step (1) obtain again, obtains mixed solution;
(3) titanium-containing compound is joined in the mixed solution that step (2) obtains, obtain catalyst component.
12. preparation method according to claim 11, wherein in every mole of organo-magnesium compound, titanium-containing compound is 0.01～10 mole; The hydroxyl compounds is 0.1～20 mole; Chloride silicoorganic compound are 0.1～50 mole; The concentration of property-modifying additive in reaction system is controlled at 0.001～100 grams per liter.
13. preparation method according to claim 11, wherein in every mole of organo-magnesium compound, titanium-containing compound is 0.05～5 mole; The hydroxyl compounds is 0.2～10 mole; Chloride organo-aluminium compound is 0.5～20 mole; The concentration of property-modifying additive in reaction system is controlled at 0.01～50 grams per liter.
14. a catalyzer that is used for equal polymerization of a-alkene or copolymerization, it comprises the reaction product of following component:
(a) the described catalyst component that is used for olefinic polymerization of one of claim 1-9;
(b) at least a general formula is AlR " '
3Organo-aluminium compound, R in the formula " ' be identical or different C
1-8Alkyl, one of them or two alkyl can be replaced by chlorine.
15. the application of the said catalyzer of claim 13 in equal polymerization of a-alkene or copolymerization.
16. according to the application of the said catalyzer of claim 14 in equal polymerization of a-alkene or copolymerization, described alkene is ethene, propylene, butylene, hexene and/or octene.
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 201010511310 CN102453126B (en) | 2010-10-19 | 2010-10-19 | Catalyst component for olefin polymerization, preparation method and application thereof |
| EP11817655.1A EP2607388B1 (en) | 2010-08-19 | 2011-08-19 | Catalytic composition for polymerization of olefin and preparation method thereof |
| MYPI2013000458A MY163741A (en) | 2010-08-19 | 2011-08-19 | Cataltic component for polymerization of olefin and preparation method thereof |
| BR112013003741-5A BR112013003741B1 (en) | 2010-08-19 | 2011-08-19 | CATALYST COMPONENT FOR OLEFINE POLYMERIZATION, ITS PREPARATION METHODS, CATALYST FOR OLEFINE COPOLIMERIZATION OR HOMOPOLIMERIZATION, AND ITS USE |
| PCT/CN2011/001389 WO2012022127A1 (en) | 2010-08-19 | 2011-08-19 | Catalytic composition for polymerization of olefin and preparation method thereof |
| US13/817,610 US9068025B2 (en) | 2010-08-19 | 2011-08-19 | Catalyst component for polymerization of olefin and preparation method |
| RU2013111930/04A RU2575167C2 (en) | 2010-08-19 | 2011-08-19 | Catalytic composition, intended for olefin polymerisation and method for obtaining thereof |
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| CN 201010511310 CN102453126B (en) | 2010-10-19 | 2010-10-19 | Catalyst component for olefin polymerization, preparation method and application thereof |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104277148A (en) * | 2013-07-01 | 2015-01-14 | 中国石油化工股份有限公司 | Catalyst component for olefin polymerization and preparation method and application thereof |
| CN107810057A (en) * | 2015-06-19 | 2018-03-16 | 沙特阿拉伯石油公司 | Antifouling oligomerisation catalyst system |
| CN107880176A (en) * | 2016-09-30 | 2018-04-06 | 中国石油化工股份有限公司 | Catalytic component and its preparation and application for olefinic polymerization |
| CN107880164A (en) * | 2016-09-30 | 2018-04-06 | 中国石油化工股份有限公司 | Catalytic component and its preparation and application for olefinic polymerization |
| CN107880186A (en) * | 2016-09-30 | 2018-04-06 | 中国石油化工股份有限公司 | Catalytic component and its preparation and application for olefinic polymerization |
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| CN1359395A (en) * | 1999-05-27 | 2002-07-17 | 三星综合化学株式会社 | Catalyst for ethylene homo-and co-polymerization |
| EP1187857B1 (en) * | 1999-06-07 | 2004-01-21 | Eastman Chemical Company | Process for producing ethylene/olefin interpolymers |
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| CN104277148A (en) * | 2013-07-01 | 2015-01-14 | 中国石油化工股份有限公司 | Catalyst component for olefin polymerization and preparation method and application thereof |
| CN107810057A (en) * | 2015-06-19 | 2018-03-16 | 沙特阿拉伯石油公司 | Antifouling oligomerisation catalyst system |
| CN107810057B (en) * | 2015-06-19 | 2021-06-04 | 沙特阿拉伯石油公司 | Antifouling oligomerization catalyst system |
| CN107880176A (en) * | 2016-09-30 | 2018-04-06 | 中国石油化工股份有限公司 | Catalytic component and its preparation and application for olefinic polymerization |
| CN107880164A (en) * | 2016-09-30 | 2018-04-06 | 中国石油化工股份有限公司 | Catalytic component and its preparation and application for olefinic polymerization |
| CN107880186A (en) * | 2016-09-30 | 2018-04-06 | 中国石油化工股份有限公司 | Catalytic component and its preparation and application for olefinic polymerization |
| CN107880176B (en) * | 2016-09-30 | 2020-07-24 | 中国石油化工股份有限公司 | Catalyst component for olefin polymerization and preparation and application thereof |
| CN107880164B (en) * | 2016-09-30 | 2020-07-24 | 中国石油化工股份有限公司 | Catalyst component for olefin polymerization and preparation and application thereof |
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