Claims
- 1. Catalyst component for polymerizing .alpha.-olefins, said catalyst component prepared by the steps of
- (a) reacting a magnesium alkyl compound with chlorine gas,
- (b) dissolving the thus-formed chlorinated magnesium alkyl compound in alcohol,
- (c) adding magnesium silicate which has not been calcinated, to the thus-formed solution,
- (d) adding the resulting mixture obtained in step (c) into a hydrocarbon medium, at a temperature under about 0.sqroot. C., thereby precipitating the chlorinated magnesium alkyl compound into and onto the magnesium silicate,
- (e) separating the obtained solid catalyst component, and
- (f) reacting the obtained solid catalyst component from step (e), with a titanium halogen compound in the presence of an internal electron donor,
- whereby isotacticity of polypropylene polymerized in the presence of the thus-formed catalyst component is greater than isotacticity of propylene polymerized in the presence of a catalyst component formed with calcinated magnesium silicate.
- 2. The component of claim 1, prepared with the additional step of
- (a') washing the thus-formed chlorinated magnesium alkyl compound prior to step (b).
- 3. A catalyst for polymerizing .alpha.-olefines, prepared by the step of
- (g) contacting the component obtained in step (f) of claim 1, with an Al-compound and an external electron donor.
- 4. A method for producing a catalyst component for polymerizing .alpha.-olefines, comprising the steps of
- (a) reacting a magnesium alkyl compound with chlorine gas,
- (b) dissolving the thus-formed chlorinated magnesium alkyl compound in alcohol,
- (c) adding magnesium silicate which has not been calcinated, to the thus-formed solution,
- (d) adding the resulting mixture obtained in step (c) into a hydrocarbon medium at a temperature under about 0.degree. C., thereby precipitating the chlorinated magnesium alkyl compound into and onto the magnesium silicate,
- (e) separating the obtained solid catalyst component, and
- (f) reacting the obtained solid catalyst component from step (e), with a titanium halogen compound in the presence of an internal electron donor,
- whereby isotacticity of propylene polymerized in the presence of the thus-formed catalyst component is greater than isotacticity of propylene polymerized in the presence of a catalyst component formed with calcinated magnesium silicate.
- 5. The method of claim 4, comprising the additional step of
- (a') washing the thus-formed chlorinated magnesium alkyl compound prior to step (b).
- 6. The method of claim 4, comprising the additional step of
- (g) contacting the component obtained in step (f), with an Al-compound and an external electron donor.
- 7. The method of claim 4, wherein the magnesium silicate added in step (c), is a mixture of silica and magnesium oxide or a coprecipitate of silica and magnesium oxide.
- 8. The method of claim 4, wherein the magnesium silicate added in step (c) is precipitated from magnesium sulfate or magnesium chloride and sodium silicate.
- 9. The method of claim 4, wherein the magnesium alkyl compound reacted in step (a) is butyl-octyl magnesium.
- 10. The method of claim 4, comprising the additional step of
- (a') adding to a precipitate formed in step (a) an amount of alcohol to thicken the precipitate and which is then washed out prior to step (b).
- 11. The method of claim 4, wherein step (f) is performed in two stages, with the internal electron donor being added in the first stage thereof.
- 12. The method of claim 4, wherein the internal electron donor present in step (f) is di-isobutyl phthalate.
- 13. The method of claim 11, wherein starting temperature in the first stage of step (f) is under about 0.degree. C., and temperature in the second stage of step (f) is about 90.degree.-110.degree. C.
- 14. The method of claim 4, wherein step (a) is carried out at a temperature at about -10.degree. to 100.degree. C.
- 15. The method of claim 14, wherein the temperature in step (a) is about 10.degree. to 60.degree. C.
- 16. The method of claim 4, wherein step (c) is carried out at a temperature of about 60.degree.-70.degree. C.
- 17. The method of claim 4, wherein step (c) is carried out for about 3-24 hours.
- 18. The method of claim 4, wherein temperature of the cold medium in step (d) is about -30.degree. to -5.degree. C.
- 19. The catalyst of claim 1, wherein
- (a) the magnesium alkyl compound is reacted with the chlorine gas for about 10-25 minutes.
- 20. The method of claim 4, wherein
- (a) the magnesium alkyl compound is reacted with the chlorine gas for about 10-25 minutes.
- 21. The method of claim 15, comprising the additional step
- (a') after step (a) is completed, treating the resulting reaction mixture with nitrogen for about 15-60 minutes to ensure complete chlorination.
Priority Claims (1)
Number |
Date |
Country |
Kind |
863930 |
Sep 1986 |
FIX |
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Parent Case Info
This is a continuation of application Ser. No. 102,136, filed Sept. 29, 1987 and now abandoned.
US Referenced Citations (5)
Continuations (1)
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Number |
Date |
Country |
Parent |
102136 |
Sep 1987 |
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