US 3,985,677 AGrant
Preparation of Polymerization Catalyst and Polymerization Therewith
Issue Date:1976-10-12
•2 Claims
Abstract
A method of polymerizing butadiene and/or butadiene in mixture with other diolefins to form polymers with a high cis-1,4 addition wherein the improvement relates to improved catalysts for producing the high cis-1,4-polybutadiene.
Metadata
Assignee
- The Goodyear Tire & Rubber Company
Inventors
- Morford C. Throckmorton
- Paul H. Sandstrom
Application Information
Application Number:US 482119&
Filing Date:1974-06-24
Priority Date:1972-10-27
Art Unit:115
Classifications
IPC:
C08F 414
Field of Search:
252260429 B94.3;84.1
Patent Drawings
This patent does not have any drawings.
Description
Example I
Three preformed catalysts were prepared; the first contained no polymeric catalyst stabilizer, the second contained 0.81 gram of butadiene monomer and the third contained 0.81 gram of high cis-1,4-polybutadiene as polymeric catalyst stabilizers. To prepare the catalysts, 21 and 13 milliliters of benzene were added respectively to the bottles in which the first and second catalysts were to be prepared. The butadiene monomer was added as 8.1 ml. of a butadiene in benzene solution, and the polybutadiene was added as 21 ml. of a solution which had been prepared by dissolving 2 grams of polybutadiene rubber in 50 ml. of benzene. Then 4 ml. of 0.5 molar triethylaluminum (TEAL), 3 ml. of 0.05 molar nickel octoate (NiOct), and 7 ml. of 0.25 molar boron trifluoride etherate (BF.sub.3.Et.sub.2 O) complex were syringed in that order into each of the three bottles. After the components were mixed the catalysts were permitted to stand at room temperature (25.degree. C.) for an hour before they were evaluated.
The catalysts were evaluated by syringing 1.75 ml. of the above solutions into a series of bottles containing 10 grams of butadiene in 100 ml. of a purified butadiene in benzene premix solution. This was equivalent to 0.4 gram of either butadiene or polybutadiene plus TEAL:NiOct:BF.sub.3.Et.sub.2 O = 1.0:0.075:0.87 millimole per 100 g. butadiene in the premix. The capped bottles were placed in a water bath maintained at 50.degree. C. and tumbled end-over-end for 1 hour. The polymerizations were terminated by adding triisopropanolamine and an antioxidant. The polymers were dried under vacuum to constant weight. The results are shown in Table 1.
Example Ii
The polymerizations were conducted in a manner relatively similar to that described in Example I except that the preformed catalysts were prepared using different polymers derived from conjugated dienes as polymeric catalyst stabilizers, and they are compared with a preformed catalyst which contained no polymeric catalyst stabilizer.
The yields columns show the percent conversion comparing the activity of the various polymer stabilized catalysts with the nonstabilized catalyst when fresh and after aging for one day.
The microstructures of four of the polymers prepared using polymeric catalyst stabilizers listed in Table 2 were determined by infrared analysis, and in every instance the polymers contained approximately 97% cis-1,4-polybutadiene and about 1.5% each of trans-1,4 and 1,2-polybutadiene. Catalysts containing stabilizers B, C, D, E and G produced polymers analyzing respectively, 97.4, 97.2, 97.4, 97.6 and 98.0 percent cis-1,4-polybutadiene.
Example Iii
The polymerizations were conducted in a manner similar to that described in Example I, except for the method of preparing the polymeric stabilized preformed catalyts used in these experiments. In this instance, two polymeric stabilized preformed catalysts were prepared using high cis-1,4-polybutadiene cements, which had not been stopped or dried, as the polymeric catalyst stabilizers. The polybutadiene cements used as polymeric catalyst stabilizers were prepared by charging "in situ" amounts of TEAL:NiOct:BF.sub.3.Et.sub.2 O equal to 1.1:0.05:0.75 millimole per 100 g. of butadiene and permitting the polymerization to proceed for 18 hours, or about 95 percent conversion. One bottle of cement contained 2.5 gram of polybutadiene as a five percent cement in benzene while a second bottle contained 5.0 gram of polybutadiene as a 10 percent cement. Then 1.3 ml. of 0.17 molar NiOct, 2.7 ml. of 1.0 molar TEAL and 2.25 ml. of 1.0 molar BF.sub.3.Et.sub.2 O were added in that order to each of the cements.
One thirtieth (1.9 ml.) of the volume of these polymeric stabilized preformed catalysts were used to initiate polymerization of fresh butadiene-benzene premix. Thus the catalyst charge from these two preformed catalysts was 0.83 and 1.67 grams, respectively, of polybutadiene plus NiOct:TEAL:BF.sub.3.Et.sub.2 O=0.075:0.90:0.75 millimole per 100 gram of butadiene in the fresh premix.
The pertinent polymerization results are presented in Table 3.
Example Iv
The following table illustrates how a liquid polybutadiene polymer which has been washed and extracted serves as a polymeric catalyst stabilizer.
The liquid polybutadiene was prepared using solution polymerization techniques and a catalyst comprising a nickel compound and ethyl aluminum sesquichloride. The resulting polymer had a molecular weight of 2600 and was liquid-like in flow characteristics.
Example V
Four grams of dried styrene-butadiene copolymer (stabilizer D in Table 2) were dissolved in 100 ml. of benzene, and aliquots of this solution containing 0.053, 0.106, 0.21 and 1.6 gram of SBR were used to prepare a series of four polymeric stabilized preformed catalysts. Aliquots of these catalysts and of a nonstabilized catalyst were evaluated by polymerizing butadiene, using the procedure described in Example I. The amount of copolymer charged varied as reported in Table 5, column 2, while the amount of the other catalyst components was uniform at NiOct/TEAL/BF.sub.3.Et.sub.2 O = 0.075/1.0/0.87 millimole per 100 grams of butadiene in the premix. The catalysts were evaluated when freshly prepared and after aging at 25.degree. C. for 1 day. The polymerizations were run for 2 hours. Results are summarized in Table 5.
Example Vi
Emulsion polymerized SBR (SBR-1502) was evaluated as a stabilizer for preformed catalyst in a manner similar to that described in Example V. Results are summarized in Table 6.
While certain representative embodiments and details have been shown for the purpose of illustrating the invention, it will be apparent to those skilled in this art that various changes and modifications may be made therein without departing from the spirit and scope of the invention.
Claims
What is claimed is:
1. In a composition suitable for use as a catalyst comprising (1) at least one organoaluminum compound, (2) at least one organonickel compound selected from the group consisting of nickel salts of carboxylic acids, organic complex compounds of nickel, and nickel tetracarbonyl, and (3) at least one fluorine compound selected from the group consisting of hydrogen fluoride, boron trifluoride, complexes of hydrogen fluoride and complexes of boron trifluoride, said complexes prepared by complexing hydrogen fluoride and/or boron trifluoride with a member of the class consisting of ketones, esters, ethers, alcohols, nitriles and water, the improvement comprising preforming said catalyst by mixing the catalyst components in the presence of a polymeric catalyst stabilizer selected from the group consisting of polymers derived from the homopolymerization of hydrocarbon conjugated diolefins, the copolymerization of hydrocarbon conjugated diolefins and the copolymerization of hydrocarbon conjugated diolefins with styrene or methyl substituted styrene, said catalyst being prepared or preformed in such a manner that said polymeric catalyst stabilizer is added to the mixture before the reaction between the organoaluminum compound and the organonickel compound, in which the mole ratio of the organoaluminum compound/organonickel compound ranges from about 0.3/1 to about 200/1, the mole ratio of the fluoride compound/organoaluminum compound ranges from about 0.2/1 to about 10/1 and the weight ratio of the polymeric catalyst stabilizer to the nickel in the organonickel compound ranges from about 2/1 to about 2000/1.
2. In the method of preparing a stabilized catalyst composition which comprises mixing (1) at least one organoaluminum compound, (2) at least one organonickel compound selected from the group consisting of nickel salts of carboxylic acids, organic complex compounds of nickel, and nickel tetracarbonyl, and (3) at least one fluorine compound selected from the group consisting of hydrogen fluoride, boron trifluoride, complexes of hydrogen fluoride and complexes of boron trifluoride, said complexes prepared by complexing hydrogen fluoride and/or boron trifluoride with a member of the class consisting of ketones, ethers, esters, alcohols, nitriles and water, the improvement comprising preforming said catalyst by mixing the catalyst components in the presence of a polymeric catalyst stabilizer selected from the group consisting of polymers derived from the homopolymerization of hydrocarbon conjugated diolefins, the copolymerization of hydrocarbon conjugated diolefins and the copolymerization of hydrocarbon conjugated diolefins with styrene or methyl substituted styrene, said catalyst being prepared or preformed in such a manner that said polymeric catalyst stabilizer is added to the mixture before the reaction between the organoaluminum compound and the organonickel compound, in which the mole ratio of the organoaluminum compound/organonickel compound ranges from about 0.3/1 to about 200/1, the mole ratio of the fluoride compound/organoaluminum compound ranges from about 0.2/1 to about 10/1 and the weight ratio of the polymeric catalyst stabilizer to the nickel in the organonickel compound ranges from about 2/1 to about 2000/1.
Patent Citations (3)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US3464965 | 1969-09-01 | Yasunaga et al. | |
| US3471462 | 1969-10-01 | Matsumoto et al. | |
| US3483177 | 1969-12-01 | Throckmorton |