← Back to Patent Explorer
US4235984A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for producing highly stereoregular α-olefin polymers

Assignee: Sumitomo Chemical Co Ltd
•
Filing: 1979-02-12
•
Granted: 1980-11-25
•
Expires: 1999-02-12
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract α-Olefin polymers of high stereoregularity are prepared by polymerizing the α-olefin with a catalyst prepared by mixing components (A), (B) and (C): (A) a solid titanium component prepared from an organo-magnesium compound, a silicon halide compound and/or an aluminum halide compound, an electron donor and TiCl 4 , (B) an organoaluminum activator, and (C) an electron donor.

Inventors

  • 👤 Akinobu Shiga
  • 👤 Yoshiharu Fukui
  • 👤 Katsumi Hanji
  • 👤 Toshio Sasaki
  • 👤 Masahisa Okawa
  • 👤 Hideaki Matsuura
  • 👤 Yasuharu Yamada

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 17:13
CPC Classifications
C; C08; C08F; C08F10/00

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 455 words
A process for producing a highly stereoregular α-olefin polymer which comprises polymerizing an α-olefin with a catalyst system comprising three components A, B and C: A: a solid catalyst produced as follows: (1) an organo-magnesium compound represented by the general formula RMgX, wherein R is C 1 -C 8 alkyl, aryl or alkenyl group and X is a halogen atom, synthesized in the presence of an ether (I) solvent is reacted in solution is said ether with at least one halogen-containing compound of (a) and (b), (a) halogeno-silicon compounds of the formula R.sub.n.sup.1 SiX.sub.4-n wherein R 1 is a C 1 -C 8 alkyl, aryl or alkenyl group, X is a halogen atom and n is a number satisfying 0≦n<4, (b) halogeno-aluminium compounds of the formula R.sub.l.sup.2 AlX.sub.3-l wherein R 2 is a C 1 -C 8 alkyl, aryl or alkenyl group, X is a halogen atom and l is a number satisfying 0≦l<3, at 0° to 100° C. in the former to the latter molar ratio of 1:10 to 10:1, and the resulting solid product is separated from the reaction system and washed with an inert hydrocarbon solvent, thereby obtaining a solid product containing 20 to 60% by weight of said ether (I), (2) the solid product is reacted, at -50° to 150° C., with an electron donor of 10 -5 to 0.1 mole per gram of solid product, selected from the group consisting of amines, amides, ethers, esters, alcohols, phenols, ketones, nitriles, phosphines, phosphites, sulfides, and lactones, and the resulting solid carrier is separated from the reaction system and washed with an inert hydrocarbon solvent, thereby obtaining a solid carrier containing 1 to 30% by weight of the ether (I) and 1 to 20% by weight of the electron donor, and (3) the solid carrier is reacted with titanium tetrachloride of 0.01 to 10 moles per gram of solid carrier at 0° to 150° C., and the resulting solid catalyst is separated from the reaction system and washed with an inert hydrocarbon solvent, thereby obtaining a solid catalyst containing 0.1 to 15% by weight of the ether (I) and 0.1 to 10% by weight of the electron donor and 0.1 to 20% by weight of titanium, B: an activating agent of the formula, R.sub.m.sup.3 AlY.sub.3-m where R 3 is a C 1 -C 8 alkyl, aryl or alkenyl group, Y is a halogen or hydrogen atom and m is a number satisfying 2≦m≦3 and C: an electron donor selected from the group consisting of amines, amides, ethers, esters, alcohols, phenols, ketones, nitriles, phosphines, phosphites, sulfides, and lactones, the molar ratio of titanium to activating agent being 10:1 to 1:500 and the molar ratio of titanium to electron donor (c) being 10:1 to 1:500.
Claim 2
Dependent Claim 455 words
A process for producing a highly stereoregular α-olefin polymer which comprises polymerizing an α-olefin with a catalyst system comprising three components A, B and C: A: a solid catalyst produced as follows: (1) an organo-magnesium compound represented by the general formula RMgX, wherein R is C 1 -C 8 alkyl, aryl or alkenyl group and X is a halogen atom, synthesized in the presence of an ether (I) solvent is reacted in solution is said ether with at least one halogen-containing compound of (a) and (b), (a) halogeno-silicon compounds of the formula R.sub.n.sup.1 SiX.sub.4-n wherein R 1 is a C 1 -C 8 alkyl, aryl or alkenyl group, X is a halogen atom and n is a number satisfying 0≦n<4, (b) halogeno-aluminium compounds of the formula R.sub.l.sup.2 AlX.sub.3-l wherein R 2 is a C 1 -C 8 alkyl, aryl or alkenyl group, X is a halogen atom and l is a number satisfying 0≦l<3, at 0° to 100° C. in the former to the latter molar ratio of 1:10 to 10:1, and the resulting solid product is separated from the reaction system and washed with an inert hydrocarbon solvent, thereby obtaining a solid product containing 20 to 60% by weight of said ether (I), (2) the solid product is reacted, at -50° to 150° C., with an electron donor of 10 -5 to 0.1 mole per gram of solid product, selected from the group consisting of amines, amides, ethers, esters, alcohols, phenols, ketones, nitriles, phosphines, phosphites, sulfides, and lactones, and the resulting solid carrier is separated from the reaction system and washed with an inert hydrocarbon solvent, thereby obtaining a solid carrier containing 1 to 30% by weight of the ether (I) and 1 to 20% by weight of the electron donor, and (3) the solid carrier is reacted with titanium tetrachloride of 0.01 to 10 moles per gram of solid carrier at 0° to 150° C., and the resulting solid catalyst is separated from the reaction system and washed with an inert hydrocarbon solvent, thereby obtaining a solid catalyst containing 0.1 to 15% by weight of the ether (I) and 0.1 to 10% by weight of the electron donor and 0.1 to 20% by weight of titanium, B: an activating agent of the formula, R.sub.m.sup.3 AlY.sub.3-m where R 3 is a C 1 -C 8 alkyl, aryl or alkenyl group, Y is a halogen or hydrogen atom and m is a number satisfying 2≦m≦3 and C: an electron donor selected from the group consisting of amines, amides, ethers, esters, alcohols, phenols, ketones, nitriles, phosphines, phosphites, sulfides, and lactones, the molar ratio of titanium to activating agent being 10:1 to 1:500 and the molar ratio of titanium to electron donor (c) being 10:1 to 1:500.
Claim 3
Dependent Claim 21 words
A process according to claim 1, wherein said ether (I) is diethyl ether, n-propyl ether, di-n-butyl ether, di-iso-amyl ether or tetrahydrofuran.
Claim 4
Dependent Claim 14 words
A process according to claim 1, wherein the organo-magnesium compound is an alkylmagnesium chloride.
Claim 5
Dependent Claim 13 words
A process according to claim 1, wherein said halogeno-silicon compound is silicon tetrachloride.
Claim 6
Dependent Claim 21 words
A process according to claim 1, wherein said halogeno-aluminum compound is anhydrous aluminum trihalide, alkylaluminum dihalide dialkylaluminum halide or alkylalauminum sesquihalide.
Claim 7
Dependent Claim 27 words
A process according to claim 1, wherein said electron donor used for the production of the solid carrier is a amine, amide, alcohol, ether or ester compound.
Claim 8
Dependent Claim 14 words
A process according to claim 6, wherein the electron donor is an ester compound.
Claim 9
Dependent Claim 24 words
A process according to claim 1, wherein said activating agent as a component B is trialkylaluminum or a mixture of trialkylalauminum and dialkylaluminum halide.
Claim 10
Dependent Claim 18 words
A process according to claim 1, wherein said electron donor as a component C is an ester compound.

References Cited (Backward Citations)

US4115319A Cited
US4159256A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-11-25 1984-05-26 1984-11-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-11-25 1988-05-26 1988-11-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-11-25 1992-05-26 1992-11-25 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag