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Preparation of homopolymers of ethene and copolymers of ethene with higherα-monolefins using a Ziegler catalyst system

Assignee: BASF SE
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Filing: 1986-06-18
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Granted: 1987-12-01
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Expires: 2006-06-18
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Abstract

Abstract Homopolymers and copolymers of ethene are prepared using a Ziegler catalyst system comprising (1) a transition metal catalyst component, (2) an organoaluminum catalyst component and (3) an organohalogen catalyst component, by a method in which the transition metal catalyst component (1) employed is a solid-phase product (VI) obtained by (1.1) first combining (1.1.1) an inorganic oxidic substrate (I), as the carrier, with (1.1.2) a solution (II) consisting of (IIa) a certain oxahydrocarbon and (IIb) a mixture of (IIb1) a vanadium trichloride/alcohol complex, (IIb2) a titanium trihalide or titanium trihalide/alcohol complex and, if required, (IIb3) a zirconium tetrahalide to form a suspension (III), evaporating down this suspension to form a solid-phase intermediate (IV), and (1.2) then (1.2.1) combining the solid-phase intermediate (IV) obtained from (1.1) with (1.2.2) a solution of an organoaluminum compound (V) to form a suspension, the resulting suspended solid-phase product (VI) being the transition metal catalyst component (1).

Inventors

  • 👤 Robert Bachl
  • 👤 Volker Warzelhan
  • 👤 Guenther Schweier
  • 👤 Hans Gropper
  • 👤 Wolfgang Ball

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 16:59
CPC Classifications
C; C08; C08F; C08F10/00; C08F10/02; Y; Y10; Y10S; Y10S526/00; Y10S526/901

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 131 words
A process for the preparation of copolymers of ethylene with minor amounts of C 3 -C 8 -α-monoolefins by polymerization of the monomers at from 50° to 125° C. and under a pressure of from 5 to 60 bar, the improvement which comprises using a Ziegler catalyst system comprising (1) a transition metal catalyst component, (2) an organoaluminum catalyst component of the formula AIR.sub.3 where R is C 2 -C 8 -alkyl, and (3) an organohalogen catalyst component (cocatalyst), selected from the group consisting of those of the formulae CFCl 3 , CCl 4 , CHCl 3 , CH 2 Cl 2 , CF 2 Cl 2 , CH 2 ═CH--CH 2 Cl, CCl 2 ═CCl--CCl 3 , CH.tbd.C--CH 2 Cl, α-chlorotoluene, α,α-dichlorotoluene, α,α,α-trichlorotoluene, methyl perchlorocrotonate and n-butyl 2,3, 4, 4-tetrachlorobut-2-enoate
Claim 2
Dependent Claim 131 words
A process for the preparation of copolymers of ethylene with minor amounts of C 3 -C 8 -α-monoolefins by polymerization of the monomers at from 50° to 125° C. and under a pressure of from 5 to 60 bar, the improvement which comprises using a Ziegler catalyst system comprising (1) a transition metal catalyst component, (2) an organoaluminum catalyst component of the formula AIR.sub.3 where R is C 2 -C 8 -alkyl, and (3) an organohalogen catalyst component (cocatalyst), selected from the group consisting of those of the formulae CFCl 3 , CCl 4 , CHCl 3 , CH 2 Cl 2 , CF 2 Cl 2 , CH 2 ═CH--CH 2 Cl, CCl 2 ═CCl--CCl 3 , CH.tbd.C--CH 2 Cl, α-chlorotoluene, α,α-dichlorotoluene, α,α,α-trichlorotoluene, methyl perchlorocrotonate and n-butyl 2,3, 4, 4-tetrachlorobut-2-enoate
Claim 3
Dependent Claim 405 words
with the provisos that the atomic ratio of the transition metal from the catalyst component (1) to aluminum from the catalyst component (2) is from 1:0.2 to 1:50, and the molar ratio of the organoaluminum catalyst component (2) to the organohalogen catalyst component (3) is from 1:0.01 to 1:10, wherein the transition metal catalyst component (1) used is a solid-phase product (VI), obtained by a method in which (1.1) first (1.1.1) a finely divided, porous silicon dioxide (I), which has a particle diameter of from 1 to 400 μm, a pore volume of from 1 to 2.5 cm 3 /g and a specific surface area of from 200 to 400 m 2 / g and (1.1.2) a solution (II), as obtained on combining (11a) 100 parts by weight of a saturated alicyclic oxahydrocarbon of 1 oxa oxygen atom and 4 to 6 carbon atoms an (11b) from 1 to 50 parts by weight of a mixture of (11b1) 100 molar parts of a vanadium trihalide/alcohol complex of the formula VY 3 .nZ-OH, wherein Y is chlorine, n is from 1 to 6, and Z is an alkyl of not more than 6 carbon atoms, (IIb2) from 0.5 to 100 molar parts of a titanium trichloride or of a titanium trihalide/alcohol complex of the formula TiY 3 .nZOH, where Y is chlorine, n is from 1 to 6 and Z is an alkyl of not more than 4 carbon atoms and (IIb3) from 3 to 200 molar parts of a zirconium tetrachloride, are brought into contact with one another to form a suspension (III), with the proviso that the weight ratio of silicon dioxide (I) to transition metal composition (IIb) is from 1:0.2 to 1:1.5, the suspension (III) is evaporated to dryness at below 160° C. and above the melting point of the oxahydrocarbon (IIa) used, a solid-phase intermediate (IV) being formed, and (1.2) thereafter (1.2.1) the solid-phase intermediate (IV) obtained from stage (1.1) and (1.2.2) a solution, in an organic solvent, of an aluminum compound (V) of the formula AIR.sub.m X.sub.3-m where X is chlorine, R is C 2 -C 8 -alkyl, and m is the number 2, are brought into contact with one another to form a suspension, with the proviso that the weight ratio of the solid-phase intermediate (IV) to the aluminum compound (V) is from 1:0.1 to 1:1, and the resulting suspended solid-phase product (VI) is the transition metal catalyst component (1).
Claim 4
Dependent Claim 405 words
with the provisos that the atomic ratio of the transition metal from the catalyst component (1) to aluminum from the catalyst component (2) is from 1:0.2 to 1:50, and the molar ratio of the organoaluminum catalyst component (2) to the organohalogen catalyst component (3) is from 1:0.01 to 1:10, wherein the transition metal catalyst component (1) used is a solid-phase product (VI), obtained by a method in which (1.1) first (1.1.1) a finely divided, porous silicon dioxide (I), which has a particle diameter of from 1 to 400 μm, a pore volume of from 1 to 2.5 cm 3 /g and a specific surface area of from 200 to 400 m 2 / g and (1.1.2) a solution (II), as obtained on combining (11a) 100 parts by weight of a saturated alicyclic oxahydrocarbon of 1 oxa oxygen atom and 4 to 6 carbon atoms an (11b) from 1 to 50 parts by weight of a mixture of (11b1) 100 molar parts of a vanadium trihalide/alcohol complex of the formula VY 3 .nZ-OH, wherein Y is chlorine, n is from 1 to 6, and Z is an alkyl of not more than 6 carbon atoms, (IIb2) from 0.5 to 100 molar parts of a titanium trichloride or of a titanium trihalide/alcohol complex of the formula TiY 3 .nZOH, where Y is chlorine, n is from 1 to 6 and Z is an alkyl of not more than 4 carbon atoms and (IIb3) from 3 to 200 molar parts of a zirconium tetrachloride, are brought into contact with one another to form a suspension (III), with the proviso that the weight ratio of silicon dioxide (I) to transition metal composition (IIb) is from 1:0.2 to 1:1.5, the suspension (III) is evaporated to dryness at below 160° C. and above the melting point of the oxahydrocarbon (IIa) used, a solid-phase intermediate (IV) being formed, and (1.2) thereafter (1.2.1) the solid-phase intermediate (IV) obtained from stage (1.1) and (1.2.2) a solution, in an organic solvent, of an aluminum compound (V) of the formula AIR.sub.m X.sub.3-m where X is chlorine, R is C 2 -C 8 -alkyl, and m is the number 2, are brought into contact with one another to form a suspension, with the proviso that the weight ratio of the solid-phase intermediate (IV) to the aluminum compound (V) is from 1:0.1 to 1:1, and the resulting suspended solid-phase product (VI) is the transition metal catalyst component (1).
Claim 5
Dependent Claim 27 words
The process of claim 1 wherein component IIa is tetrahydrofuran; in component IIb1 n is 3 or 4; and in component IIb2 n is 3 or 4.
Claim 6
Dependent Claim 43 words
The process of claim 1 wherein component (IIb2) consists solely of a titanium trihalide/alcohol complex of the formula TiY 3 -nZOH, where Y is chlorine, n is from 1 to 6, and Z is an alkyl of not more than 4 carbon atoms.

References Cited (Backward Citations)

CA716176A Cited
US3723348A Cited
GB1309565A Cited
US4098979A Cited
GB1582287A Cited
US4151337A Cited
DE3242149A1 Cited
DE3242150A1 Cited
US4508842A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-11-30 1991-06-01 1991-12-01 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-11-30 1995-06-01 1995-12-01 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-11-30 1999-06-01 1999-12-01 $7700.00 Window Closed / Lapsed

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