Claims
- 1. A process comprising polymerizing olefins in the presence of a polymerization catalyst and a cocatalyst wherein said cocatalyst is prepared by a process comprising forming a mixture of:
- (a) a chromium compound selected from the group consisting of chromium salts having the formula CrX.sub.n wherein "X" can be the same or different and is an organic or inorganic radical and "n" is an integer from 1 to 6, and chromium metal;
- (b) a metal amide selected from the group consisting of alkali metal amide salts, alkaline earth metal amide salts, and mixtures thereof; and
- (c) an ether;
- wherein said cocatalyst is a trimerization or oligomerization catalyst system and wherein said cocatalyst is different from said polymerization catalyst system.
- 2. A process according to claim 1 wherein said polymerization catalyst is a supported chromium catalyst.
- 3. A process according to claim 1 wherein said polymerization catalyst is a titanium-containing catalyst.
- 4. A process according to claim 1 wherein said cocatalyst comprises a chromium compound selected from the group consisting of Cr.sub.5 (C.sub.4 H.sub.4 N).sub.10 (C.sub.4 H.sub.8 O).sub.4 ; Cr(C.sub.4 H.sub.4 N).sub.4 ; �Cr(C.sub.4 H.sub.4 N).sub.4 !�Na!.sub.2.2(OC.sub.4 H.sub.8); �Cr(C.sub.4 H.sub.4 N).sub.5 OC.sub.4 H.sub.8 !; �Cr(C.sub.44).sub.5 OC.sub.48 !�Na!.sub.2.4(OC.sub.4 H.sub.8); and mixtures thereof.
- 5. A process according to claim 1 wherein said cocatalyst is supported on an inorganic oxide.
- 6. A process according to claim 1 wherein said olefin has from 2 to about 30 carbon atoms per molecule.
- 7. A process according to claim 6 wherein said olefin is selected from the group consisting of ethylene, propylene, 1-butene, 1-hexene, and mixtures thereof.
- 8. A process according to claim 7 wherein said olefin is predominantly ethylene.
- 9. A process according to claim 1 wherein said polymerization is carried out at a temperature within the range of about 66.degree. to about 110.degree. C.
- 10. A process according to claim 1 wherein hydrogen is present during said polymerization process.
- 11. A process according to claim 1 wherein said polymerization process is a slurry polymerization process.
- 12. A process according to claim 1 wherein a polymer is recovered.
- 13. A process according to claim 1 wherein said olefin is ethylene and wherein a polymer is recovered which has a density within the range of about 0.9 g/cc to about 0.96 g/cc.
- 14. A process according to claim 1 wherein said metal amide has from about 1 to about 20 carbon atoms per molecule.
- 15. A process according to claim 1 wherein said metal amide is an unsaturated compound.
- 16. A process according to claim 15 wherein said metal amide is an aromatic compound.
- 17. A process according to claim 1 wherein said metal amide has an amine ligand and wherein said amine ligand is selected from the group consisting of pyrrolide ligands, derivatives of pyrrole ligands, and mixtures thereof.
- 18. A process comprising polymerizing olefins in the presence of a polymerization catalyst and a cocatalyst wherein said cocatalyst is prepared by a process comprising forming a mixture of and refluxing:
- (a) a chromium compound selected from the group consisting of chromium salts having the formula CrX.sub.n wherein "X" can be the same or different and is an organic or inorganic radical and "n" is an integer from 1 to 6, and chromium metal;
- (b) a metal amide selected from the group consisting of alkali metal amide salts, alkaline earth metal amide salts, and mixtures thereof; and
- (c) an electron pair donor solvent;
- wherein said cocatalyst is a trimerization or oligomerization catalyst system and wherein said cocatalyst is different from said polymerization catalyst system.
- 19. A process according to claim 18 wherein said chromium compound is selected from the group consisting of chromium acids, chromium halides, and mixtures thereof.
- 20. A process according to claim 19 wherein said chromium compound is a chromium halide selected from the group consisting of chromous chloride, chromic chloride, and mixtures thereof.
- 21. A process according to claim 18 wherein said metal amide has from about 1 to about 20 carbon atoms per molecule.
- 22. A process according to claim 18 wherein said metal amide is an unsaturated compound.
- 23. A process according to claim 22 wherein said metal amide is an aromatic compound.
- 24. A process according to claim 18 wherein said metal amide has an amine ligand and wherein said amine ligand is selected from the group consisting of pyrrolide ligands, derivatives of pyrrole ligands, and mixtures thereof.
- 25. A process according to claim 18 wherein said electron pair donor solvent has from about 2 to about 20 carbon atoms per molecule.
- 26. A process according to claim 18 wherein said electron pair donor solvent is an aliphatic compound.
- 27. A process according to claim 18 wherein said metal amide is soluble in said electron pair donor solvent.
- 28. A process according to claim 18 wherein said electron pair donor solvent is an ether and is selected from the group consisting of tetrahydrofuran, derivatives of tetrahydrofuran, dimethoxyethane, derivatives of dimethoxyethane, and mixtures thereof.
- 29. A process according to claim 18 wherein said mixture is maintained in a liquid state.
- 30. A process according to claim 29 wherein said mixture is maintained in a liquid state for a time in the range of about 1 minute to about 1 week.
Parent Case Info
This application is a division of application Ser. No. 08/109,855, filed Aug. 20, 1993, now U.S. Pat. No. 5,451,645, the entirety of which is herein incorporated by reference; which is a continuation of application Ser. No. 07/807,309, filed Dec. 13, 1991, now abandoned, the entirety of which is herein incorporated by reference; which is n continuation-in-part of application Ser. No. 07/698,631, filed May 10, 1991, now abandoned, the entirety of which is herein incorporated by reference; which is a continuation-in-part of Ser. No. 07/393,354, filed Aug. 10, 1989, now abandoned, the entirety of which is herein incorporated by reference.
US Referenced Citations (39)
Foreign Referenced Citations (2)
Number |
Date |
Country |
2253029 |
Dec 1973 |
FRX |
45-24153 |
Aug 1970 |
JPX |
Non-Patent Literature Citations (9)
Entry |
Zeitschrift fur Naturfroschung, Pyrrolylchromium Compounds, 21 b, p. 1239 (D. Tille, 1996). |
Z. Anorg. Alleg. Chem., Organometal Compounds of Nitrogen Systems, 384, pp. 136-146 (D. Tille, 1971). |
J. Chem. Soc., Chem. Commun., Selective Trimerization of Ethylene to Hex-1-ene, pp. 674,5 (J. Briggs, 1989). |
Morrison, R.T. and Boyd, R.N., Organic Chemistry (1980) pp. 729 and 730. |
Solomons, T.W.G., Organic Chemistry (1976) p. 818. |
Satterfield, C.N., Heterogeneous Catalysis in Practice pp. 68-77. |
Le Page, J.F. et al., Applied Heterogeneous Catalysis (1978) pp. 90-96. |
Leach, B.E. (Ed), Applied Industrial Catalysis (1984) pp. 13-14 and 25-37. |
Hegedus, L.L. (Ed.), Catalyst Design Progress and Perspectives (1985) pp. 112-127. |
Divisions (1)
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Number |
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Parent |
109855 |
Aug 1993 |
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Continuations (1)
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Date |
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Parent |
807309 |
Dec 1991 |
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Continuation in Parts (2)
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Date |
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Parent |
698631 |
May 1991 |
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Parent |
393354 |
Aug 1989 |
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