WO2005100410A1 - オレフィン重合体の製造方法 - Google Patents
オレフィン重合体の製造方法 Download PDFInfo
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- WO2005100410A1 WO2005100410A1 PCT/JP2005/006729 JP2005006729W WO2005100410A1 WO 2005100410 A1 WO2005100410 A1 WO 2005100410A1 JP 2005006729 W JP2005006729 W JP 2005006729W WO 2005100410 A1 WO2005100410 A1 WO 2005100410A1
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- methylene
- zirconium dichloride
- compound
- polymerization
- cyclopentagenenyl
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/645—Component covered by group C08F4/64 with a metal or compound covered by group C08F4/44, not provided for in a single group of groups C08F4/642 - C08F4/643
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/04—Polymerisation in solution
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/642—Component covered by group C08F4/64 with an organo-aluminium compound
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/943—Polymerization with metallocene catalysts
Definitions
- the present invention relates to a method for solution polymerization of olefins at a temperature of from 120 to 300 ° C. in the presence of a catalyst comprising a metamouth compound having a specific structure.
- a method for producing an olefin polymer such as an ethylene Z-olefin copolymer
- a method using a Ziegler-type titanium catalyst comprising a titanium compound and an organoaluminum compound is widely known.
- a catalyst capable of producing an olefin polymer with high polymerization activity a meta-mouth catalyst comprising a transition metal compound such as zirconocene and an organoaluminoxy compound (hereinafter sometimes referred to as “aluminoxane”) may be used. Since the method of polymerizing olefins in the presence of a system catalyst has been reported [eg, Adv. Organomet. Chem. L899 (1980) and Angew.
- JAEwen disclosed for the first time an olefin polymerization using a novel meta-metacene compound in which a cyclopentajenyl ligand and a fluorenyl ligand were crosslinked, which had never existed before. Contributed to a considerable extent [J. Am. Chem. So, 110, 6255 (1988)].
- a metadensene compound having a cyclopentadenyl group as a ligand was copolymerized under high-pressure and high-temperature conditions to obtain a relatively high-density polymer.
- a method for producing a styrene / 1-hexene copolymer has been disclosed [JP-A-1-503788. Also, Japanese Patent Application Laid-Open No. 5-320246 discloses that dicyclopentajenyl There is disclosed a method for producing an ethylene 1-otaten copolymer at an elevated temperature by using mucichloride and dimethyl arinidium tetra (pentafluoropheninole) boron.
- these disclosed methods have a problem that it is difficult to obtain a polymer having a high molecular weight in a low-density region (that is, a region having a high comonomer content). Further, further improvement is required also from the viewpoint of polymerization activity. Disclosure of the invention
- the present invention has been made to solve the above-mentioned problems, and a high-molecular-weight polymer can be obtained with a high polymerization activity that could not be achieved conventionally, and when the polymer is a copolymer,
- Another object of the present invention is to provide a method for producing a high molecular weight olefin polymer having a high comonomer content, a narrow composition distribution, and a narrow molecular weight distribution. That is, the present invention
- Rl, R 2, R3, R4, R5, R8, R9 and R12 are hydrogen atom, a hydrocarbon group, may be people NOTE - selected from Kei Moto ⁇ organic groups are identical or different, groups with adjacent R6 and R11 may be the same atom or the same group selected from hydrogen, a hydrocarbon group, and a silicon-containing group, and may be bonded to each other to form a ring.
- R 7 and Rio are the same atom or the same group selected from hydrogen, a hydrocarbon group and a silicon-containing group, and may be bonded to each other to form a ring; R 6 and R 7 , Rio and R "are not hydrogen atoms at the same time.
- R 13 and R 14 may be the same or different from each other a Ariru group.
- M is Ti, Zr or Hf, preferably Zr or Hf.
- Y is carbon or silicon;
- Q is coordinated by halogen, hydrocarbon group, anion ligand or lone electron pair It may be selected from ability neutral ligands in the same or different combinations,;.
- J is an integer from 1 to 4)
- the present invention is a.
- a solution of one or more monomers selected from ethylene and olefins in the presence of a solvent at a temperature of 120 to 300 ° C in the presence of a catalyst for polymerization of olefins comprising at least one compound selected from Polymerization (hereinafter sometimes referred to as “high-temperature solution polymerization”) produces high-molecular-weight olefin polymers having properties useful in various industrial fields such as films and various molded bodies.
- the cross-linked meta-acene compound according to the present invention an olefin polymerization catalyst containing the cross-linked metallocene compound, a method of performing high-temperature solution polymerization in the presence of the olefin polymerization catalyst, and characteristics of a polymer obtained by the high-temperature solution polymerization, BEST MODE FOR CARRYING OUT THE INVENTION
- BEST MODE FOR CARRYING OUT THE INVENTION The best mode for carrying out the invention will be described sequentially.
- cross-linked meta-mouth compound (A) The cross-linked meta-acene compound represented by the general formula [I] has the following features in the chemical structure, [ml] to [m3].
- the two ligands are linked by a covalent cross-link containing a carbon atom having an aryl group or a silicon atom (hereinafter sometimes referred to as an “aryl group-containing covalent cross-link”). ing.
- the transition metal (M) that constitutes the meta-acene compound is titanium, zirconium, or hafnium.
- the cyclopentagenenyl group, the fluorenyl group, the cross-linking portion, and other characteristics which are the chemical structural characteristics of the cross-linked meta-mouth compound according to the present invention will be sequentially described, and then a preferable cross-linked meta-port having both of these characteristics will be described.
- the high-temperature solution polymerization method of the present invention using the cross-linked meta-mouth compound is described in detail below.
- the cyclopentajenyl group may or may not be substituted.
- the cyclopentagenenyl group which may or may not be substituted is a force in which Rl, R 2 , R 3 and R 4 of the cyclopentenyl group moiety in the above general formula [I] are all hydrogen atoms, Or one or more of RR 2 , R 3 and R 4 is a hydrocarbon group (fl), preferably a hydrocarbon group having 1 to 20 carbon atoms (fl ′), or a silicon-containing group (f2 ), Preferably a cyclopentadenyl group substituted with a silicon-containing group (f2 ′) having a total of 1 to 20 carbon atoms.
- the hydrocarbon group having a total of 1 to 20 carbon atoms is an anolequinole, alkule, alkynyl, or aryl group composed of only carbon and hydrogen. This includes those in which any two adjacent hydrogen atoms are simultaneously substituted to form an alicyclic or aromatic ring.
- Hydrocarbon groups (fl ') having 1 to 20 carbon atoms in total include alkyl, alkenyl, alkynyl, aryl groups consisting of only carbon and hydrogen.
- a heteroatom-containing hydrocarbon group in which some of the hydrogen atoms directly bonded to carbon are substituted with a halogen atom, an oxygen-containing group, a nitrogen-containing group, or a silicon-containing group, or any two adjacent hydrogen atoms Include those forming an alicyclic group.
- Such groups ( ⁇ ') include methyl, ethyl, n-propyl, allyl, n-butyl, n-pentyl, n-hexyl, n-heptyl, linear hydrocarbon groups such as n-octyl, n-noninole and n-decanyl; isopropyl, t-butyl, amyl, 3-methylpentyl, 1,1-getylpropyl, 1,1-dimethylbutyl group, 1-methyl_1-propylbutyl group, 1,1-propylbutyl group, 1,1-dimethyl-2-methylpropyl group, 1-methyl-1-isopropyl-2-methylpropyl
- a cyclic hydrocarbon group such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a norbornyl group or an
- cyclic unsaturated coals A hydrogen group or a substituted alkyl thereof; a saturated hydrocarbon group substituted with an aryl group such as a benzyl group or a cumyl group; a methoxy group, an ethoxy group, a phenyl group; an n-oxy group; an N-methylamino group; a trifluoromethyl group; Hetero atom-containing hydrocarbon groups such as a bromomethyl group, a pentafluoroethyl group and a pentafluorophenyl group can be exemplified.
- the silicon-containing group (f2) is, for example, a group in which a ring carbon of a cyclopentagenenyl group is directly and covalently bonded to a silicon atom, and specifically, is an alkylsilyl group or a arylsilyl group.
- Examples of the silicon-containing group (f2 ′) having a total carbon number of 1 to 20 include a trimethylsilyl group and a triphenylsilyl group.
- R 6 and Rii in the general formula [I] are hydrogen, hydrocarbon group ( fl) and the same atom or the same group selected from the silicon-containing groups (f2), which may be bonded to each other to form a ring.
- R 7 and Rio are hydrogen, a hydrocarbon group (fl), R 6 , R 7 , Rio and Rii may be the same atom or the same group selected from the hydrogen-containing group (f2) and may be bonded to each other to form a ring; Polymerization in high temperature solution polymerization of the present invention From the viewpoint of activity, it is preferable that R 6 and R "are not both hydrogen, and that R 6 , R 7 , Rio and Rii are not all hydrogen atoms.
- R 6 and Rii are a hydrocarbon group and a silicon-containing group. It is particularly preferred that R 7 is the same group selected from a hydrocarbon group and a silicon-containing group.
- a preferable example of the silicon-containing group (f2) is the above-described silicon-containing group (1) having a total carbon number of 1 to 20.
- the main chain of the bond connecting the cyclopentagenenyl group and the fluorenyl group is a divalent covalent crosslink containing one carbon atom or a silicon atom.
- An important point in the high temperature solution polymerization of the present invention is that the bridging atom Y of the covalently crosslinked portion has an aryl group [R13 and R14] which may be the same or different from each other.
- the Ariru group, phenyl group, a naphthyl group, anthra cell - le groups and can be one or more of these aromatic hydrogen (sp 2 type hydrogen) illustrate been substituted with a substituent.
- the substituent include the aforementioned hydrocarbon group having 1 to 20 carbon atoms (fl ′), the aforementioned silicon-containing group having 1 to 20 carbon atoms (f2 ′), and a halogen atom.
- aryl groups include phenyl, tolyl, t-butylphenyl, dimethylphenyl, biphenyl, cyclohexylphenyl, (trifluoromethyl) phenyl, and bis (trifluoromethyl) phenyl.
- the component (B) which is a component of the olefin polymerization catalyst according to the present invention includes (b-1) an organic aluminum dimethoxy compound and Z or (b-3 ) Organic aluminum compound is used
- (b-2) a compound which forms an ion pair by reacting with the cross-linked meta-mouth compound (A) is not used.
- Q is a halogen, a hydrocarbon group having 1 to 10 carbon atoms, or a neutral, conjugated or non-conjugated gen, anion ligand or isolated having 10 or less carbon atoms. It is selected from neutral ligands that can coordinate with electron pairs in the same or different combinations.
- halogen include fluorine, chlorine, bromine and iodine
- hydrocarbon group include methyl, ethyl, n-propyl, isopropyl, 2-methylolepropyl, 1,1-dimethylpropyl, 2 1,2-dimethylpropyl, 1,1-getylpropynole, 1-ethyl-1-methylpropyl, 1,1,2,2-tetramethylpropyl, sec-butyl, tert-butynole, 1,1-dimethylinobutynole , 1,1,3-trimethylbutyl, neopentyl, cyclohexylmethyl, cyclohexyl, 1-methyl-1-cyclohexyl and the like.
- anion ligand examples include an alkoxy group such as methoxy, tert-butoxy and phenoxy, a carboxylate group such as acetate and benzoate, and a sulfonate group such as mesylate and tosylate.
- neutral ligands capable of coordinating with a lone electron pair include organic phosphorus compounds such as trimethylphosphine, triethynolephosphine, triphenylphosphine, diphenylmethylphosphine, and tetrahydrofuran, methyl ether, dioxane, 1 And ethers such as 2-dimethoxyethane.
- I is an integer of 1 to 4, and when j is 2 or more, Qs may be the same or different.
- octamethyloctahydrodibenzofluorene refers to a compound having a structure represented by the formula [II]
- octamethyltetrahydrodicyclopentafluorene refers to a compound represented by the formula
- dibenzofluorene refers to the compound having the structure represented by the formula [IV]
- 1, ⁇ , 3,6,8,8'-hexamethyl-2,7- Dihydrodicyclopentafluorenyl refers to a compound having the structure represented by the formula [V], and includes 1,3,3 ', 6,6', 8-hexamethyl-2,7-dihydrodicyclopentafluorenyl Means a compound having the structure represented by the formula [VI].
- Noreconidum dichloride di (be Dolodizenzofur reninole) zirconium dichloride, di (benzhydr / le) methylene (cyclopentageninoleactamethyltetrahydrodicyclopentafluorenyl) zirco dimethyl dichloride, di-fcuminole) methylene (cyclopentagenenyl) 2,7-ditert-butylfluorenyl) dinoreconicum dichloride, di (cumyl) methylene (cyclopentadenyl) (3,6- Di-tert-butylfluoreninole) zirconium dichloride, di (cumyl) methylene (cyclopentagenenyl) octamethyloctahydrodibenzofluorenyl) zirconium dimethyl dichloride, di (cumyl) methylene (cyclopentagenenyl) (Benzofunolelenyl) di-noreconi
- I-cyclopenta-geni / j is replaced by (3-tert-butyl-5-methyl-cyclopentagenenyl) J or "(3,5-dimethyl-cyclopentagenyl)” , “(3-tert-butynole-cyclopentageninole)”, “(3-methynole-cyclopentageninyl)”, etc. It is a meta-mouth compound related to a polymerization method.
- the (A) cross-linked meta-acene compound of the present invention can be produced by a known method, and the production method is not particularly limited.
- Known production methods include, for example, WO01 / 27174 by the present applicant and WO04 / 029062.
- the catalyst component is (A) a crosslinked methacrylate compound represented by the above formula [I], (B) (b-1) ) Organoaluminum oxy compound, (b-2) the cross-linked meta-mouth compound
- component (B) of the following [cl] to [c4] or component (B) is preferably used.
- component (B) As the component (B), (b-2) a compound capable of forming an ion pair by reacting with the self-bridged meta-mouthen compound (A) is not used. Therefore, the preferred component (B) described above;
- the organoaluminoxy compound used in the present invention may be a conventionally known Aluminoxane can be used as it is. Specifically, the following general formula [VII]
- R represents a hydrocarbon group having 1 to 10 carbon atoms, and n represents an integer of 2 or more.
- methylaluminoxane which is an R-methyl group
- n is 3 or more, preferably 10 or more.
- metaloaluminoxy compound in which R is a methyl group in the general formula [VII] or [VIII] may be hereinafter referred to as “methinoleanoreminoxane”.
- Methylaluminoxane is an organoaluminoxy compound that has been widely used in the polyolefin industry because of its availability and high polymerization activity.However, since it is difficult to dissolve in saturated hydrocarbons, methylaluminoxane has a large environmental load. It has been used as an aromatic hydrocarbon solution such as benzene and benzene. against this background, methylaluminoxane analogs soluble in saturated hydrocarbons have been developed. Examples of such analogs include modified methylaluminoxane as shown in the following [IX].
- the (a-1) organoaluminumoxy compound relating to the high-temperature solution polymerization method of the present invention also includes such a modified methylanolenominoxane.
- R is a hydrocarbon group having 2 to 20 carbon atoms, and m and n each represent an integer of 2 or more.
- the modified methylaluminoxane represented by the general formula [IX] is other than trimethylaluminum and trimethylaluminum.
- the production method is disclosed in US4960878, US5041584, and the like), and prepared from a manufacturer such as Toso I. Finechem Co., Ltd. using trimethylanoleminium and triisobutylaluminum.
- Those in which R is an isobutyl group are commercially produced under trade names such as MM AO and TMAO (see, for example, “Tosoichi Research 'Technical Report”, Vol.
- MMAO or TMAO cannot be polymerized in the form of a saturated hydrocarbon solution outside the technical range of the high-temperature solution polymerization method of the present invention to achieve an activity exceeding that of methylaluminoxane.
- a high polymerization activity is found even when a saturated hydrocarbon solution of the modified aluminoxane represented by the general formula [IX] is used. This point is also one of the features of the high temperature solution polymerization method of the present invention.
- a benzene-insoluble organic aluminoxy compound exemplified in JP-A-2-78687 can also be applied.
- examples of the organic aluminum oxy compound used in the present invention include an organic aluminum oxy compound containing boron represented by the following general formula [X]. r, c
- Rc represents a hydrogen atom having 1 to 10 carbon atoms.
- R d may be the same or different and may be a hydrogen atom, a halogen atom or a carbon atom having 1 to 10 carbon atoms. Represents a hydrogen group.
- the organic aluminum compound may contain some organic aluminum compound.
- (b-2) A compound that forms an ion pair by reacting with the cross-linked meta-mouth compound (A)
- a compound (b-2) that reacts with the cross-linked meta-mouth compound (A) to form an ion pair And may be abbreviated as an “ionic compound.”
- the ionic compounds include: JP-A-1-501950, JP-A-1-502036, JP-A-3_179005, JP-A-3-179006, Examples thereof include Lewis acids, ionic compounds, borane compounds and carborane compounds described in Kaihei 3-207703, JP-A-3-207704, US Pat. No. 5,321,106. Further, heteropoly compounds and isopoly compounds can also be mentioned.
- the ionic compound preferably employed is a compound represented by the following general formula [XI].
- examples of R e + include H + , carbenium cation, oxonium cation, ammonium cation, phosphonium cation, cycloptinoletrenyl cation, and feline mouth cation having a transition metal.
- R f to Ri may be mutually the same or different and are an organic group, preferably an aryl group.
- carbeum cation examples include 1, tri-substituted carbedium cations such as rifenylcarbenyl cation, tris (methylphenyl) carbamate cation, and tris (dimethylphenylenole) carbamate.
- carbeum cation examples include 1, tri-substituted carbedium cations such as rifenylcarbenyl cation, tris (methylphenyl) carbamate cation, and tris (dimethylphenylenole) carbamate.
- ammonium cation examples include a trimethyl ammonium cation, a triethyl ammonium cation, a tri (n-propyl) ammonium cation, a triisopropyl ammonium cation, and a tri (11-butyl) cation.
- Trialkylammonium cations such as ammonium cation and triisobutylammonium cation, ⁇ , ⁇ -dimethylaniline cation, ⁇ , ⁇ -Jetylaniline cation, ⁇ , ⁇ -2, And dialkylammonium cations such as 6-, ⁇ ⁇ ⁇ -dialkylanilumium cation such as 4,6-pentamethylaniline cation, disopropionoleammonium cation and dicyclohexylene ammonium cation.
- phosphonium cation examples include triarylphosphonium cations such as triphenylphosphonium cation, tris (methylphenyl) phosphonium cation, and tris (dimethylphenyl) phosphonium cation.
- a carbenium cation, an ammonium cation, and the like are preferable, and in particular, a triphenylcarbenium cation, a ⁇ , ⁇ ⁇ ⁇ ⁇ -dimethylanilinium cation, and a ⁇ , ⁇ -methylethylaniline cation Cations are preferred.
- carbamate salt examples include triphenyl-carbenetetraf-m-dipropylate, triphenylcarbamatetetrakis (pentafluoropheninole) borate, and triphenylcarbenyltetramethylenetetrakis (3,5-ditrifluoromethylphene).
- Nore) borate g Lis (4-methylpheninole) carbedemtetrakis (pentafluorophenyl) borate Tris (3,5-dimethylpheninole) carbedenetetrakis (pentafluorophenylene) borate and the like can be mentioned.
- ammonium salts include trialkyl-substituted ammonium salts, ⁇ , ⁇ -dialkylanilinium salts, dialkylammonium salts and the like.
- trialkyl-substituted ammonium salts include, for example, triethylammoniumtetraphenylborate, tripropylammoniumtetraphenylporate, tri ( ⁇ -butyl) ammoniumtetraphenylporate, and tritylammonium-tetramethylperoxide ( ⁇ - Tolyl) borate, trimethylammonium tetrakis fo-tolyl) borate, tri (n-butyl) ammonium tetrakis (pentafluoropheninole, borate, triethylammonium tetrakis (pentafluorophenylinole) borate, tripropro Pinoleammonium temrakis (pentafluoropheninole) borate, trippropinoleammonium tetrakis (2,4-dimethylphenyl) borate, tri (n-butyl) ammonium
- ⁇ , ⁇ -dialkylanilinium salt examples include ⁇ , ⁇ -dimethylaniliniumtetraphenylborate and ⁇ , ⁇ -dimethylaniliniumtetrakispentapentafluorophenyl) borate , ⁇ , ⁇ -dimethylaniluiumtetrakis (3,5-ditrifluoromethylpheninole) borate, ⁇ , ⁇ -jetinorea dilicume tetraphenylinoleborate ⁇ , ⁇ -Jetylaniliniumtetrakis (pentafluorophenol) borate, ⁇ , ⁇ -Jetylaniliniumtetrakis (3,5-ditrifluoromethinolefeninole) borate, ⁇ , ⁇ -2,4,6-pentamethylauri-dimethyltetraphenyl borate, ⁇ , ⁇ -2,4,6-pentamethylanilinium tetraki
- dialkylammonium salt examples include di (1-propyl) ammoniumtetrakis (pentafluoropheninole) borate, dicyclohexylammoniumtetraphenylphenolate, and the like.
- JP-A-2004-516766 ionic compounds disclosed by the present applicant (JP-A-2004-51676) can be used without limitation.
- the above ionic compound (b-2) can be used as a mixture of two or more kinds.
- organoaluminum compound (b-3) that forms the olefin polymerization catalyst
- organoaluminum compound (b-3) that forms the olefin polymerization catalyst
- organoaluminum compound represented by the following general formula [XII] an organoaluminum compound represented by the following general formula [XII]
- group 1 metal represented by the following general formula [XIII] aluminum And complex alkylated compounds.
- Ra and Rb may be the same or different from each other, and the number of carbon atoms is
- X represents a halogen atom
- the organoaluminum compound represented by) include tri-n-alkylaluminums such as trimethylaluminum, triethylaluminum, tri-n-butylaluminum, trihexylaluminum, and trioctylaluminum; triisopropylaluminum, triisoaluminum, and trisec-aluminum.
- Tri-branched alkyl aluminum such as butylaluminum, tritert-butylaluminum, tri2-methylbutylaluminum, tri3-methylhexylaluminum, tri2-ethylhexylaluminum; tricyclohexylanoleminium
- Tricycloalkyl aluminum such as tricyclooctyl aluminum
- triaryl aluminum such as triphenyl aluminum and tritolyl aluminum
- Dialkyl aluminum such as butyl aluminum hydride -Pemhydride; represented by the general formula (iC 4 H 9 ) x Aly (C 5 Hi 0 ) z (where x, y, and z are positive numbers and z ⁇ 2x).
- Alkenyl aluminum such as isoprenyl aluminum
- alkyl aluminum alkoxide such as isobutyl aluminum methoxide and isobutyl aluminum methoxide
- dialkyl aluminum alkoxide such as dimethyl aluminum methoxide, dimethyl aluminum ethoxide and dibutyl aluminum butoxide
- E chill aluminum sesqui ethoxide, heptyl aluminum Yu arm sesqui Bed alkyl sesquichloride such butoxide Anore Koki Sid;..
- M 2 represents a Li, Na or K
- R a is from 1 to 15 carbon atoms, preferably:!.
- ⁇ shows a 4 hydrocarbon group
- a compound similar to the compound represented by the above general formula [XII] can also be used.
- a compound having two or more aluminides bonded via a nitrogen atom is also available.
- Such ingredients manner as compounds, and the like (C 2 H5) 2A1N (C2H5 ) A1 (C 2 H5) 2.
- (b-3) trimederluminum and triisobutylaluminum are preferably used as the organoaluminum compound.
- At least two or more of the catalyst components may be in pre-contact.
- the component (A) is usually used in an amount of 10-9 to: 10-1 mol, preferably 10 to 8 mol per liter of the reaction volume. used in such an amount that the 10 2 moles.
- Component (b-1) has a ratio ((bl) / M) of component (b-1) to all transition metal atoms (M) in component (A) of usually 0.01 to 5,000, preferably 0.05 to 5,000. It is used in such an amount as to be 2,000.
- Component (b-2) has a molar ratio [(b-2) / M] of the aluminum atom in component (b-2) to the transition metal (M) in component (A) of 10 to 5,000. It is preferably used in such an amount as to give 20 to 2,000 O.
- the component (b-3) has a molar ratio [(b-3) / M] of the component (b-3) to the transmetal atom (M) in the component (A) of usually:! To 10,000, preferably Is used in such an amount as to become!
- the olefins applicable to the high-temperature solution polymerization reaction are one or more monomers selected from ethylene and ⁇ -olefins.
- ethylene is used as an essential olefin, and carbon atoms may be added as necessary.
- 3 ⁇ 4 (co) polymerization of at least one kind of olefin selected from 3 to 20 olefins
- the charged moles of ethylene and ⁇ -olefin having 3 to 20 carbon atoms are used.
- ⁇ -olefins having 3 to 20 carbon atoms include linear or branched ⁇ -olefins having 3 to 10 carbon atoms, such as propylene, 1-butene, 2-butene, 1-pentene, 3-methyl-1-butene, 1-hexene, 4-methynole-1-pentene, 3-methyl-1-pentene, 1-otaten, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, etc.
- the olefins that can be used in the high temperature solution polymerization of the present invention also include olefins containing a polar group.
- Examples of the polar group-containing olefin include metal salts such as ⁇ ,] 3-unsaturated carboxylic acids such as acryloline acid, methacrylic acid, fumaric acid, and maleic anhydride, and sodium salts thereof; methyl acrylate, acrylic acid ⁇ , ⁇ -unsaturated carboxylic esters such as ethyl, ⁇ -propyl acrylate, methyl methacrylate, and ethyl methacrylate; vinyl esters such as butyl acetate and vinyl propionate; glycidyl acrylate and glycidyl methacrylate Saturated glycidyls and the like can be mentioned.
- metal salts such as ⁇ ,] 3-unsaturated carboxylic acids such as acryloline acid, methacrylic acid, fumaric acid, and maleic anhydride, and sodium salts thereof; methyl acrylate, acrylic acid ⁇ , ⁇ -unsaturated carboxylic esters such as
- aromatic cyclocompounds such as styrene, 0-methylstyrene, m-methylstyrene, ⁇ -methylstyrene, ⁇ , ⁇ -dimethylstyrene, methoxystyrene, vinylbenzoic acid, and butylbenzoic acid.
- Styrenes such as methyl acrylate, vinylbenzyl acetate, hydroxystyrene, ⁇ -chlorostyrene, and divinyl / madzene; and 3-phenylpropylene, 4-phenylpropylene, and para-methylstyrene coexist in the reaction system. It is also possible to proceed with high temperature solution polymerization.
- olefins propylene, 1-butene, 1-hexene, 4-methyl-1-pentene and 1-octene are preferably used.
- a cyclic olefin having 3 to 30, preferably 3 to 20 carbon atoms for example, cyclopentene, cycloheptene, norbornene, 5-methyl-2-norbornene, and tetracyclododecene are used in combination. May be.
- the 'Solution polymerization' of the present invention is a general term for a method of performing polymerization in a state in which a polymer is dissolved in an inert hydrocarbon solvent described below at a temperature equal to or higher than the melting point of the polymer.
- the polymerization temperature is usually 120 ° C. to 300 ° C., preferably 130 ° C. to 250 ° C., more preferably 130 ° C. to 200 ° C. (as described above, this solution Polymerization is referred to herein consistently as "hot solution polymerization").
- the polymerization temperature is lower than 120 ° C., the polymerization activity is extremely reduced, and thus it is not practical in terms of productivity. Further, in the polymerization temperature region of 120 ° C. or higher, as the temperature increases, the solution viscosity during polymerization decreases, the heat of polymerization heat can be easily removed, and the molecular weight of the obtained olefin polymer can be increased. However, if the polymerization temperature exceeds 300 ° C., the resulting polymer may deteriorate, which is not preferable.
- the polymerization temperature is preferably used in many industrial fields such as a film in the region of 120 to 200 ° C. This makes it possible to efficiently produce the ethylene polymer described below.
- the polymerization pressure is usually from normal pressure to lOMPa gauge pressure, preferably from normal pressure to 8 MPa gauge pressure, and the polymerization reaction can be carried out by any of a batch system, a semi-continuous system and a continuous system. It is also possible to carry out the polymerization in two or more stages under different reaction conditions.
- the molecular weight of the obtained olefin polymer can also be adjusted within the scope of the present invention by changing the hydrogen concentration and the polymerization temperature in the polymerization system. Furthermore, it can be adjusted by the amount of the component (B) used. When hydrogen is added, the amount is suitably about 0.001 to 5,000 NL per 1 kg of the produced olefin polymer.
- the solvent used in the high-temperature solution polymerization of the present invention is usually an inert hydrocarbon solvent, preferably a saturated hydrocarbon having a boiling point of 50 ° C to 200 ° C under normal pressure.
- an inert hydrocarbon solvent preferably a saturated hydrocarbon having a boiling point of 50 ° C to 200 ° C under normal pressure.
- Specific examples include aliphatic hydrocarbons such as pentane, hexane, heptane, octane, decane, dodecane, and kerosene; and alicyclic hydrocarbons such as cyclopentane, cyclohexane, and methylcyclopentane.
- Aromatic hydrocarbons such as benzene, toluene, and xylene, and halogenated hydrocarbons such as ethylene chloride, chlorobenzene, and dichloromethane are also referred to as “inert carbons” related to the high-temperature solution polymerization of the present invention. It does not fall under the category of “hydrogen solvents” and does not limit its use.
- hydrogen solvents As described above, in the high-temperature solution polymerization of the present invention, not only the aromatic hydrocarbon dissolving type organoaluminoxy compound conventionally used but also the aliphatic hydrocarbon and the alicyclic hydrocarbon are dissolved. Modified methylaluminoxane such as MMAO can be used.
- the high-temperature solution polymerization method of the present invention also has a feature that the environmental load can be reduced and the effect on human health can be minimized.
- Olefin polymers obtained by the high temperature solution polymerization method.
- the properties of the olefin polymer produced by the high-temperature solution polymerization of the present invention are not particularly limited, but the olefin polymer obtained by the high-temperature solution polymerization of the present invention and having extremely high industrial utility value is obtained.
- preferable properties of the ethylene-based polymer will be described.
- the density of the ethylene polymer obtained by the high-temperature solution polymerization of the present invention is usually 0.85 to 0.95 g / cm3, preferably 0.86 to 0.95 g / cm3.
- the molecular weight distribution (Mw / Mn, in terms of polystyrene, Mw: weight average molecular weight, Mn: number average molecular weight) of the ethylene polymer obtained by the high temperature solution polymerization of the present invention measured by GPC is preferably 1.0 to 4.0. Is from 1.2 to 3.0, more preferably from 1.5 to 2.5.
- Ethylene polymers ethylene content obtained by the high temperature solution polymerization of the present invention, 100 to 50 Monore%, including preferably 99.9 to 65 Monore 0/0, more preferably in the range of 99.7 to 70 molar%.
- Ethylene polymers satisfying the above properties are known using Ziegler-Natta catalyst.
- the power S that can be produced by known slurry polymerization or gas phase polymerization using a polymerization catalyst containing a specific meta-acene compound the high-temperature solution polymerization of the present invention, If a method of polymerizing olefins as an inert hydrocarbon solution at a temperature of 120 to 300 ° C.
- a sheet of 0.5 mm thickness is formed at a pressure of 100 kg / cm 2 using a hydraulic heat press manufactured by Shindo Metal Industry Co., Ltd. set at 190 ° C (a spacer shape: 240 x 240 x 0.5 mm thick plate).
- 45 X 45 X 0.5 mm, 9 pieces) using another Shinto Kinzoku Kogyo's hydraulic heat press machine set at 20 ° C, measure by cooling by compressing with lOOkg / cm 2 pressure
- a sample was prepared.
- the hot plate used was a 5 mm thick SUS plate.
- the press sheet was heat-treated at 120 ° C. for 1 hour, linearly cooled to room temperature over 1 hour, and measured with a density gradient tube.
- Di (P-tolyl) methylene (cyclopentadienyl) (otatamethyloctahydrodibenzophthalenoleninole) dinoreconidum dichloride is placed in a glass flask sufficiently purged with nitrogen.
- a catalyst solution was obtained by adding 0.25 mmol.
- a 2-liter stainless steel autoclave with a sufficient nitrogen replacement was charged with 800 milliliters of hexane and 200 milliliters of 1-octene, the temperature of the system was raised to 175 ° C, and then 1000 milliliters of hydrogen were mounted.
- the total pressure was adjusted to 3MPa-G by supplying ethylene.
- 1.0 mmol of triisobutylaluminum and the above-prepared catalyst solution were pressurized with nitrogen, and the polymerization was started by rotating the stirring at 400 rpm. Thereafter, the total pressure was maintained at 3 MPa-G by continuously supplying only ethylene, and polymerization was performed at 180 ° C for 30 minutes.
- Polymerization was carried out in the same manner as in Example 2, except that the polymerization time was changed to 30 minutes using the above catalyst solution.
- a catalyst solution was obtained by adding 0.0625 millimoles of a TMAO-341 hexane solution (manufactured by Tosoh Finechem Co.) in 0.0625 mmol in A1 amount.
- Polymerization was carried out in the same manner as in Example 7, except that 950 ml of hexane and 50 ml of 1-octene were used, and the polymerization time was changed to 10 minutes.
- Di (p-trinole) methylene (cyclopentagenenyl) (octamethyloctahydrodibenzofluoreninole) zirconium dichloride is converted to di (1-naphthyl) methylene (cyclopentagenenyl) (octamethyloctahydrodiene)
- Benzofluorenyl) zirconium dichloride was changed to 0.002 mmol, the amount of ⁇ , ⁇ -dimethylaniliniumtetrakis (pentafluorophenyl) borate was changed to 0.02 mmol, and hydrogen was not added. Polymerization was performed.
- di (1-naphthyl) methylene (cyclopentagenyl) (otatamethyloctahydrodibenzofluorenyl) zirconium dichloride was placed at 0.001 millimeter, and the Albemar MAO was placed there.
- a catalyst solution was obtained by adding 0.25 mmol of the toluene solution in A1 amount.
- a 2-liter stainless steel autoclave with a sufficient nitrogen replacement was charged with 800 ml of Hexane and 200 ml of 1-otaten, and after raising the temperature of the system to 145 ° C, ethylene was supplied. The total pressure was 3MPa-G.
- 1.0 mmol of trisobutylaluminum and the catalyst solution prepared above were injected with nitrogen, and the polymerization was started by stirring at 400 rpm. Thereafter, the total pressure was maintained at 3 MPa-G by continuously supplying only ethylene, and polymerization was carried out at 150 ° C for 10 minutes.
- After terminating the polymerization by adding a small amount of ethanol into the system, unreacted ethylene was purged.
- the polymer was precipitated by pouring the obtained polymer solution into a large excess of methanol.
- the polymer was recovered by filtration and dried under reduced pressure at 135 ° C.
- Example 13 di (1-naphthyl) methylene (cyclopentagenenyl) (octamethylooctahydrodibenzofluorenyl) zirconium dichloride was converted to diphenylmethylencopened pentagenyl octamethyloctahydrodibenzozofluoreninole zirconate.
- a catalyst solution was prepared and polymerization was performed in the same manner as in Example 13 except that the amount of hydrogen charged during polymerization was changed to 1,000 ml.
- Example 13 di (1-naphthyl) methylene (cyclopentagenenyl) (Ottame tyloctahydrodibenzofluorenyl, zirconium dichloride was converted to di (p-tert-butynole-phenyl) methylene (cyclopentadenyl octamethyl) Preparation and polymerization of the catalyst solution were carried out in the same manner as in Example 13, except that the reaction mixture was changed to (octahydrodibenzofluorenyl) zirconium dichloride.
- Example 13 di (1-naphthyl) methylene (cyclopentagel) (Ottame cylooctahydrodibenzofluorenyl) zirconium dichloride was converted to di (m-trifluoro) Preparation and polymerization of a catalyst solution were carried out in the same manner as in Example 13, except that the composition was changed to (r-methyl-pheninole) methylene (cyclopentagenenyl) (octamethyloctahydrodibenzofluorenyl) zirconium dichloride.
- Example 13 di (1-naphthyl) methylene (cyclopentagenenyl) (octamethylooctahydrodibenzofluoreninole) zirconium dichloride was converted to di (p-chloro-phenyl) methylene (cyclopentagenenyl). ) A catalyst solution was prepared and polymerized in the same manner as in Example 13 except that (octamethyloctahydrodibenzozofluorenyl) zirconium dichloride was used.
- Example 13 di (1-naphthyl) methylene (cyclopentagenenyl) (octamethylooctahydrodibenzofluorenyl) zirconium dichloride was converted to di (p-biphenyl) methylene ⁇ cyclopentagenenyl) (octamethylo). Preparation and polymerization of the catalyst solution were carried out in the same manner as in Example 13, except that the reaction was changed to zirconium dichloride.
- Example 13 di (1-naphthyl) methylene (cyclopentagenenyl) (octamethylooctahydrodibenzofluoreninole) zirconium dichloride was converted to di (P-trifluoromethyl-phenyl) methylene (cyclopentagenenyl) A catalyst solution was prepared and polymerized in the same manner as in Example 13, except that (octamethyloctahydrodibenzofluorenyl) zirconium dichloride was used.
- Example 13 di (1-naphthyl) methylene (cyclopentagenenyl) (octamethylooctahydrodibenzofluoreninole) zirconium dichloride was converted to di (P-tolyl) methylene (cyclopentagenenyl) ⁇ 2, A catalyst solution was prepared and polymerized in the same manner as in Example 13, except that 7-dimethinole-3,6-ditert-butylphthalolenyl) zirconium dichloride was used.
- Example 13 di (1-naphthyl) methylene (cyclopentagenenyl) (octamethylooctahydrodibenzofluorenyl) zirconium dichloride was converted to di (p-tolyl) methylene (cyclopentagenenyl) (1,1 ′, Preparation of the catalyst solution and polymerization were carried out in the same manner as in Example 13, except that 3,6,8,8, -hexamethyl-2,7-dihydrodicyclopentafluoreninole) zirconium dichloride was used. .
- Example 13 di (1-naphthyl) methylene (cyclopentagenenyl) (octamethylooctahydrodibenzofluorenyl) zirconium dichloride was converted to di (p-tolyl) methylene (cyclopentageninole) C2,7-di
- Preparation and polymerization of a catalyst solution were carried out in the same manner as in Example 13 except that the amount of hydrogen charged during the polymerization was changed to 1,200 ml of tert-butylphenololenolinol) zirconium dichloride.
- 0.001 mmol of diphenylsilylene (cyclopentaenyl) (2,7-ditert-butylfluorenyl) zirconium dichloride was placed in a glass flask sufficiently purged with nitrogen.
- a catalyst solution was obtained by adding a toluene solution of MAO manufactured by Albemarle and adding 0.25 millimono in A1 amount.
- a 2 liter stainless steel autoclave fully purged with nitrogen is charged with 850 ml of 1-octene and 150 ml of 1-octene, and after raising the temperature of the system to 135 ° C, 200 ml of hydrogen is charged.
- the total pressure was adjusted to 3MPa-G by supplying ethylene.
- 1.0 mmol of triisobutylaluminum and the catalyst solution prepared above were injected with nitrogen, and the polymerization was started by rotating the stirring at 400 rpm. Thereafter, the pressure was maintained at 3 MPa-G by continuously supplying only ethylene, and polymerization was carried out at 140 ° C for 30 minutes. After the polymerization was stopped by adding a small amount of ethanol, unreacted ethylene was purged.
- the polymer was deposited by pouring the obtained polymer solution into a large excess of methanol. The polymer was recovered by filtration and dried at 135 ° C under reduced pressure.
- Example 23 diphenylsilylene (cyclopentajeel) (2,7-tert-butynolenorolelenylzirconium) dichloride was replaced with diphenylsilylene (cyclopentagen) (otatamethyloctahydrodibenzofluorenyl). )
- Example 12 di (1-naphthyl) methylene (cyclopentagenenyl) (octamethylooctahydrodibenzofluorenyl) zirconium dichloride was converted to di (m-trifluoromethyl-pheninole) methylene (3-methyl-5-tert) (Butyl cyclopentajeel) (2,7-ditert-butylfluoreninole) zirconium dichloride in 0.002 mmol, Albemar MAO toluene solution from A5 amount of 0.25 mmol to 0.5 mmol, polymerization time Preparation of a catalyst solution and polymerization were carried out in the same manner as in Example 12, except that was changed to 30 minutes.
- Example 12 di (1-naphthyl) methylene (cyclopentagenenyl) (otatamyl chlorooctahydrodibenzofluoreninole) zirconium dichloride was converted to diphenylmethylene (3-ethynole-5-tert-butynolecyclopentadiene).
- Preparation and polymerization of the catalyst solution were carried out in the same manner as in Example 12 except that the polymerization time was changed to (2,7)-(2,7-ditert-butynolefnorolelenyl) zirconium dichloride, except that the polymerization time was changed to .30 minutes. .
- a 2 liter stainless steel autoclave with a sufficient nitrogen displacement was charged with 800 ml of hexane and 200 ml of 1-octene, the temperature of the system was raised to 145 ° C, and then ethylene was supplied.
- the total pressure was 3MPa-G.
- polymerization was performed at 150 ° C. for 30 minutes. After the polymerization was stopped by adding a small amount of ethanol into the system, unreacted ethylene was purged. The polymer was precipitated by pouring the humiliated polymer solution into a large excess of methanol. The polymer was recovered by filtration and dried under reduced pressure at 135 ° C.
- Example 12 di (1-naphthyl) methylene (cyclopentagel) (dithiol-butyryloctahydrodibenzozofluoreninole) zirconium dichloride was converted to diphenylmethylene (3-methyl-5-tert-butynolene).
- Albemarle MAO toluene solution from 0.25 mmol in A1 amount to 0.5 mmol polymerization time
- Catalyst solution was prepared and polymerization was carried out in the same manner as in Example 12, except that was changed to 30 minutes.
- Example 23 diphenylsilylene (cyclopentagenenyl) (2,7-tert-butylphenol) was added to 0.002 mmol of simethinolemethylenecyclopentaenyl) (fluorenyl) zirconium dichloride.
- the catalyst solution was prepared and polymerized in the same manner as in Example 23 except that the toluene solution of MAO manufactured by Albemar Nore was changed from 0.25 mmol to 0.4 mmol in A1 amount, and hydrogen was not charged during polymerization.
- a catalyst solution was prepared in the same manner as in Comparative Example 1 except that dimethylmethylene (cyclopentagenenyl) (furenyl benzyl) dinorecone dichloride was changed to dimethinolesilylene (indeninole) (funolelenyl) dinoleconium dichloride in Comparative Example 1. Was prepared and polymerized.
- Example 1 O.OOl A 0.01 0.3 200 500 150 30 59.7 59.7 1.03 7.62 7.4 898 2.12
- Example 2 0.00025 B 0.0625 1 200 1500 150 10 110.7 442.8 5.37 36.00 6.7 904 2.07
- Example 3 0.001 B 0.25 1 200 1000 180 30 88.6 88.6 6.52 47.60 7.3 904 2.06
- Example 4 0.0005 C 0.125 1 200 1500 150 30 79.6 159.2 1.66 10.80 6.5 905 2.15
- Example 5 0.00025 D 0.0625 1 200 1500 150 10 80.3 321.2 4.31 27.20 6.3 904 2.11 a
- Example 6 0.001 B 0.25 1 200 700 200 30 35 35.0 7.23 905
- Example 7 0.0005 C 0.125 1 400 1500 150 8 65.8 131.6 2.80 874
- Example 8 0.0005 C 0.125 1 400 1500 140 10 85 170.0 0.79 865
- Example 2 1 i 0 5B 0.125 1 200 1500 150 30 67.9 135.8 2.15
- Example 2 2 k 0.0005 B 0.125 1 200 1200 150 30 32.5 65.0 1.21 904
- Example 2 4 m 0.001 B 0.25 1 150 200 140 30 80.9 80.9 1.40
- Example 2 5 n 0.001 B 0.25 1 200 1500 150 30 74.2 74.2 2.50
- Example 2 6 0 0.002 B 0.5 1 200 ⁇ 150 30 75.9 38.0 9.10 66.00 7.2 905 2.19
- Example 2 8 0.004 E 0.04 0.3 200 ⁇ 150 30 18.9 4.7 14.90 100.00 6.7 905 2.08 K g 1 0.002 B 0.5 1 200 ⁇ 150 30 97.5 48.8 7.84 50.50 7.1 Glue 2.15
- Tributyl isobutylaluminum is used as component (b3) for 7 £.
- n di (P-tolyl) methylene (cyclopentagenenyl) (2,7-diphenyl-3,6-ditert-butylfurenyl) zirconium dichloride
- o di (m-triflurylmethyl-phenyl) methylene (3-methino-5-tert-phthylcyclopentapentaenyl) (2,7-ditert-butylfluorenyl) zirconium dichloride
- p diphenyl Methylene (3-ethyl-5-tert-butylcyclopentagenyl) (2, -di-tert-butyl-phenyl) yl zirconium dichloride
- a copolymer having a high comonomer content and a high molecular weight olefin polymer having a narrow composition distribution and a narrow molecular weight distribution has high activity and efficiency.
- the obtained olefin polymer is a useful raw material resin in the field of various molding materials such as films, and the effect of the high-temperature solution polymerization method of the present invention on the industry is extremely large.
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Abstract
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CA002514263A CA2514263A1 (en) | 2004-03-31 | 2005-03-30 | Process for producing olefin polymers |
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US12/974,458 USRE42957E1 (en) | 2004-03-31 | 2005-03-30 | Process for producing olefin polymers |
EP05726511A EP1731533A4 (en) | 2004-03-31 | 2005-03-30 | METHOD FOR PRODUCING OLEFIN POLYMER |
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US9969827B2 (en) | 2014-02-13 | 2018-05-15 | Mitsui Chemicals, Inc. | Process for producing ethylene/α-olefin copolymer |
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WO2018151104A1 (ja) | 2017-02-20 | 2018-08-23 | 三井化学株式会社 | 積層体 |
US11964447B2 (en) | 2017-02-20 | 2024-04-23 | Mitsui Chemicals, Inc. | Laminate |
WO2019180802A1 (ja) | 2018-03-20 | 2019-09-26 | 三井化学株式会社 | エチレン・α-オレフィン・非共役ポリエン共重合体、その製造方法および用途 |
US11905348B2 (en) | 2018-03-20 | 2024-02-20 | Mitsui Chemicals, Inc. | Ethylene/alpha-olefin/non-conjugated polyene copolymer, method for producing the same, and use thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2011153315A (ja) | 2011-08-11 |
CN100523010C (zh) | 2009-08-05 |
US7741419B2 (en) | 2010-06-22 |
US20060270812A1 (en) | 2006-11-30 |
EP1731533A4 (en) | 2011-05-18 |
KR20070061567A (ko) | 2007-06-13 |
USRE42957E1 (en) | 2011-11-22 |
CN1771267A (zh) | 2006-05-10 |
CA2514263A1 (en) | 2005-09-30 |
JP5476334B2 (ja) | 2014-04-23 |
EP1731533A1 (en) | 2006-12-13 |
KR20060058670A (ko) | 2006-05-30 |
KR100738851B1 (ko) | 2007-07-12 |
JP2005314680A (ja) | 2005-11-10 |
JP5166678B2 (ja) | 2013-03-21 |
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