Conjugated diene polymerisation

• US 5,686,371 A
• Filed: 08/10/1994
• Issued: 11/11/1997
• Est. Priority Date: 09/09/1991
• Status: Expired due to Term

• Current Assignee: Enichem Elastomeri SPA
• Original Assignee: Enichem Elastomeri SPA
• Inventors: Ansell, Peter John, Williams, Hugh David
• Primary Examiner(s): Caldarola, Glenn A.
• Assistant Examiner(s): PASTERCZYK, JAMES W
• Application Number:
  US08/193,064
• Time in Patent Office: 1,189 Days
• Field of Search: 585/502, 585/506, 585/507, 585/530, 585/531, 585/532, 502/102, 502/150, 502/152, 502/154, 502/158, 526/335, 526/340.4, 526/127, 526/128
• US Class Current: 502/102
• CPC Class Codes: C08F 36/04 conjugated
• CPC Class Codes: C08F 4/58 together with silicon, germanium, tin, lead, antimony, bismuth or compounds thereof

Abstract

A process for the polymerization of one or more conjugated dienes by means of a rare earth based catalyst in which the catalyst is formed by bringing together in liquid hydrocarbon medium in the presence of a small portion of conjugated diene: a) a rare earth salt, b) an organo aluminum and c) a silicon halide or organosilicon halide and aging the catalyst before contact with the conjugated diene(s) to be polymerized. This catalyst formation procedure offers the possibility of producing a diene polymer of high cis content with a narrower molecular weight distribution and/or smaller high molecular weight fraction which is reflected in improved processing characteristics and reduced viscosity in styrene.

Claims

1. A process for the catalytic polymerization of at least one conjugated diene by a catalyst comprising a rare earth salt, an organo aluminium cocatalyst and a source of halogen, said process comprising the steps of:

(a) preparing said catalyst by bringing together, in a liquid hydrocarbon medium and in the presence of a portion of at least one conjugated diene (i) a rare earth salt, (ii) an organo aluminium compound and (iii) as the source of halogen, a silicon halide or organosilicon halide;

(b) aging said catalyst; and

(c) polymerizing at least one conjugated diene in the presence of the catalyst of step (b).

2. The process as claimed in claim 1, wherein said silicon halide or organosilicon halide is selected from the group consisting of silicon tetrachloride, silicon tetrabromide, trimethyl silyl chloride, trimethyl silyl bromide, dimethyl dichlorosilane, diphenyl dichlorosilane and methyl trichlorosilane.

3. The process as claimed in claim 1, wherein the mole ratio of halide:

rare earth salt is within the range of from 0.5;

1 to 15;

1.

4. The process as claimed in claim 3, wherein the mole ratio of halide:

rare earth salt is within the range of from 1;

1 to 10;

1.

5. The process as claimed in claim 1, wherein the mole ratio of conjugated diene:

rare earth salt in step (a) is within the range of 5;

1 to 50;

1.

6. The process as claimed in claim 1, wherein the mole ratio of conjugated diene:

rare earth salt in step (a) is within the range of 5;

1 to 40;

1.

7. The process as claimed in claim 1, wherein said rare earth salt is a hydrocarbon soluble salt of a rare earth element selected from the group consisting of cerium, lanthanum, praseodymium, gadolinium and neodymium.

8. The process as claimed in claim 7, wherein said rare earth salt is selected from the group consisting of neodymium neodecanoate, neodymium naphthenate, neodymium octanoate, neodymium 2,2-diethyl hexanoate, neodymium 2,2-diethyl heptanoate, lanthanum neodecanoate, lanthanum naphthenate, lanthanum octanoate, lanthanum 2,2-diethyl hexanoate, lanthanum 2,2-diethyl heptanoate, praseodymium neodecanoate, praseodymium naphthenate, praseodymium octanoate, praseodymium 2,2-diethyl hexanoate and praseodymium 2,2-diethyl heptanoate.

9. The process as claimed in claim 1, wherein said organo aluminium compound is selected from the group consisting of aluminium triethyl, aluminium triisobutyl and diisobutyl aluminium hydride.

10. The process as claimed in claim 1, wherein said conjugated diene of step (a) is selected from the group consisting of butadiene, isoprene, piperylene, 1,2-dimethyl butadiene, 2,3-dimethyl butadiene, myrcene, 1,3-cyclooctadiene, and 2-phenyl butadiene.

11. The process as claimed in claim 1, wherein the mole ratio of aluminium compound:

rare earth salt is within the range of from 1;

1 to 200;

1.

12. The process as claimed in claim 11, wherein the mole ratio of aluminium compound:

rare earth salt is within the range of from 5;

1 to 50;

1.

22. A process as claimed in claim 1 wherein after the catalyst is aged and prior to the polymerization of step (c), additional conjugated diene is added to the aged catalyst, which is then polymerized in step (c).

13. A catalyst useful in the catalytic polymerization of at least one conjugated diene comprising a rare earth salt, an organo aluminium cocatalyst and a source of halogen, said catalyst being prepared by bringing together, in a liquid hydrocarbon medium and in the presence of a portion of at least one conjugated diene, (i) a rare earth salt, (ii) an organo aluminium compound and (iii) as the source of halogen, a silicon halide or organosilicon halide, and aging said catalyst.

14. The catalyst as claimed in claim 13, wherein said catalyst is prepared by a process comprising the steps of:

(a) adding said aluminium compound to a liquid hydrocarbon medium;

(b) adding said rare earth salt to the mixture of step (a);

(c) adding said conjugated diene;

(d) adding said silicon halide or organosilicon halide; and

(e) aging said catalyst product of step (d).

15. The catalyst as claimed in claim 13, wherein said rare earth salt is selected from the group consisting of neodymium neodecanoate, neodymium naphthenate, neodymium octanoate, neodymium 2,2-diethyl hexanoate, neodymium 2,2-diethyl heptanoate, lanthanum neodecanoate, lanthanum naphthenate, lanthanum octanoate, lanthanum 2,2-diethyl hexanoate, lanthanum 2,2-diethyl heptanoate, praseodymium neodecanoate, praseodymium naphthenate, praseodymium octanoate, praseodymium 2,2-diethyl hexanoate and praseodymium 2,2-diethyl heptanoate.

16. The catalyst as claimed in claim 13, wherein said organo aluminium compound is selected from the group consisting of aluminium triethyl, aluminum triisobutyl and diisobutyl aluminium hydride.

17. The catalyst as claimed in claim 13, wherein said conjugated diene is selected from the group consisting of butadiene, isoprene, piperylene, 1,2-dimethyl butadiene, 2,3-dimethyl butadiene, myrcene, 1,3-cyclooctadiene, and 2-phenyl butadiene.

18. The catalyst as claimed in claim 13, wherein said catalyst is aged for a period of from 5 minutes to 6 days.

19. The catalyst as claimed in claim 18, wherein said catalyst is aged between 5 hours and 6 days.

20. The catalyst as claimed in claim 13, wherein said catalyst is formed and aged at 0°

C. to 30°

C.

21. The catalyst as claimed in claim 13, wherein said rare earth salt comprises neodymium neodecanoate, said organoaluminium compound comprises diisobutyl aluminum hydride and said source of halogen comprises silicon tetrachloride.