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Process for preparing alternating copolymer of butadiene and .alpha.-olefine and novel alternating copolymer of butadiene and .alpha.-olefine containing cis-configuration butadiene unit |
| RE28850 |
Process for preparing alternating copolymer of butadiene and .alpha.-olefine and novel alternating copolymer of butadiene and .alpha.-olefine containing cis-configuration butadiene unit
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| Patent Drawings: | |
| Inventor: |
Kawasaki, et al. |
| Date Issued: |
June 8, 1976 |
| Application: |
05/594,512 |
| Filed: |
July 9, 1975 |
| Inventors: |
Kawasaki; Akihiro (Ichihara, JA)
Maruyama; Isao (Ichihara, JA)
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| Assignee: |
Maruzen Petrochemical Co., Ltd. (Tokyo, JA) |
| Primary Examiner: |
Holler; Alan |
| Assistant Examiner: |
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| Attorney Or Agent: |
Flynn & Frishauf |
| U.S. Class: |
526/107; 526/339; 526/340; 526/98 |
| Field Of Search: |
260/84.1; 260/85.3R |
| International Class: |
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| U.S Patent Documents: |
3210332; 3317496; 3462406; 3466268; 3470144; 3506632; 3652518; 3652519; 3700638; 3714133; 3803106 |
| Foreign Patent Documents: |
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| Other References: |
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| Abstract: |
A process for preparing alternating copolymer of butadiene and .alpha.-olefine which comprises contacting butadiene and the .alpha.-olefine in liquid phase with a catalyst system comprising the first component of AIR.sub.3 wherein R represents a hydrocarbon radical selected from the group consisting of alkyl, aryl and cycloalkyl radical in which at least one R is selected from the group consisting of alkyl having at least 3 carbon atoms per one molecule, aryl and cycloalkyl radical and the second component of TiX'.sub.4 wherein X' is selected from the group consisting of chlorine, bromine and iodine, or a catalyst system comprising the first component of AlR.sub.3 wherein R represents a hydrocarbon radical selected from the group consisting of alkyl, aryl and cycloalkyl radical, and the second component of TiX'.sub.4 wherein X' is the same as that defined above and the third component of a carbonyl group-containing compound. An alternating copolymer of butadiene and .alpha.-olefine, the microstructure of butadiene unit of the alternating copolymer contains cis-configuration. The alternating copolymers are rubber-like in character and can be used as polymeric plasticizers, in adhesives and can be vulcanized with sulfur or a sulfur compound to produce vulcanized elastomers. |
| Claim: |
What we claim is:
1. A process for preparing a 1:1 copolymer of butadiene and an alpha-olefin having alternating butadiene and alpha-olefin units, said alpha-olefin having the general formula ofCH.sub.2 =CHR' wherein R' represents a phenyl radical or a C.sub.1 to C.sub.4 normal or branched chain alkyl radical, which comprises contacting butadiene and the alpha-olefin in liquid phase at a temperature of from -100.degree. C. to 50.degree. C.with a catalyst system comprising a first component of an organoaluminum compound having the general formula of AlR.sub.3 wherein R represents a hydrocarbon radical selected from the group consisting of an alkyl radical, an aryl radical and a cycloalkylradical, a second component of titanium tetrahalide having the general formula TiX'.sub.4 wherein X' is selected from the group consisting of chlorine, bromine and iodine, and a third component of a carbonyl group-containing compound, wherein the molarratio of said organoaluminum compound to said titanium tetrahalide is from greater than 1.5 to 20 and the molar ratio of butadiene to said alpha-olefin in the initial monomer composition is within a range of from 20:80 to 80:20.
2. A process as claimed in claim 1, wherein the catalyst system contains a material selected from the group consisting of a metal oxide, a metalloid oxide, a halogen and a halogen compound as a fourth component.
3. A process as claimed in claim 1, wherein the molar ratio of the organoaluminum compound to the titanium tetrahalide is approximately 1.5-10.
4. A process as claimed in claim 1, wherein said halogen compound is selected from the group consisting of a halogen compound having Lewis acid property, a Lewis acid-base complex of a halogen compound having Lewis acid property, anorganoaluminum compound having an Al-X linkage, an organotransition-metal compound having a transition metal-X linkage and an alkane compound having a C-X linkage, wherein X represents halogen.
5. A process as claimed in claim 1 wherein the polymerization reaction is carried out in the presence of a hydrocarbon diluent.
6. A process as claimed in claim 1 wherein the molar ratio of butadiene to the alpha-olefin in the initial monomer composition is substantially 50:50.
7. A process as claimed in claim 1, wherein said .alpha.-olefin is styrene.
8. A process as claimed in claim 1, wherein said .alpha.-olefin is selected from the group consisting of propylene, butene-1, pentene-1 and hexene-1.
9. A process as claimed in claim 1, werein said .alpha.-olefin is 4-methyl pentene-1. |
| Description: |
BACKGROUND OF THE INVENTION
(1) Field of the Invention
The present invention relates to a process for preparing an alternating copolymer of butadiene and .alpha.-olefine and a novel alternating copolymer obtained thereby. The novel alternating copolymer of this invention contains considerableamounts of cis-configuration butadiene unit.
(2) Description of the Prior Art
Because of its chipping and cutting properites and its low skid resistance, the demand for cis-1.4 polybutadiene in the field of automobile tires is not so large as was expected at first. The defects have been ascribed to its unbranchedstraight-chain structure. In order to overcome these defects, many attempts have been made to produce alternating copolymers of butadiene and .alpha.-olefine, for example, butadiene and propylene, butadiene and 1-butene, etc. However, in general, it isnot easy to produce even a random copolymer of butadiene and .alpha.-olefine by an ionic catalyst.
For instance, German Pat. 1,173,254 claims a process for preparing a copolymer of conjugated diene and mono-olefine using vanadium (V) oxychloride as the catalyst, but the examples do not show a copolymerization reaction of butadiene andpropylene. German Pat. 1,144,924 claims a process for preparing a copolymer of diene and ethylene or propylene by using a catalyst system consisting of a compound of Ti, Zr, Ce, V, Nb, Ta, Cr, Mo or W in which the metal is at least in part below avalency of 3. This patent shows the copolymerization reaction of butadiene and ethylene by titanium tetrachloride-lithium-aluminum hydride, titanium, tetrachloride-phenylmagnesium bromide, titanium tetrachloride-sodium dispersion, zirconium,tetrachloride-tintetrabutyl and tetraoctyltitanate-phenylmagnesium bromide catalyst systems in its examples, but a process for preparing a copolymer of butadiene and propylene is not shown. Belgian Pat. 625,657 also describes a process for preparingco- and terpolymers of butadiene with ethylene and (or) .alpha.-olefines by using a catalyst system containing a hydrocarbon-soluble vanadium compound and an organoaluminum compound containing more than one organic group having strong sterical hindrance,e.g. 3-methyl-butyl, cycloalkyl or cyclopentyl methyl, and it claims a process for preparing ethylene-propylene-butadiene terpolymer. However, no example of butadiene-propylene copolymer is shown in it.
On the other hand, British Pat. 1,108,630 shows a process for preparing a rubbery random copolymer of butadiene and propylene of high molecular weight with high content of propylene by using a three components catalyst system consisting oftrialkylaluminum, iodine and a compound having the general formula of TiBr.sub.n Cl.sub.4.sub.-n wherein n is zero or an integer of 1 to 4. The microstructure of butadiene unit and the content of propylene unit in the copolymer are shown in the patent. But there are shown no experimental results which support the assumption which the copolymer should be a random copolymer of butadiene and propylene. A random copolymer of butadiene and propylene was also prepared by using a catalyst system consistingof triethylaluminum, titanium tetrachloride and polypropylene oxide. Polypropylene oxide was used as a randomizer and therefore a copolymer of butadiene and propylene prepared by the catalyst system of triethylaluminum and titanium tetrachloride wasshown to be blocktype. The molar ratio of triethylaluminum to titanium tetrachloride was 1.08 (Al/Ti=1.08) (paper presented at 2nd Symposium on Polymer Synthesis, Tokyo, Oct. 5, 1968, the Society of Polymer Science, Japan). British Pat. 1,026,615claims a process for preparing a random copolymer of butadiene and propylene by forming a catalyst system of triethylaluminum and titanium tetrachloride in the presence of propylene, and then adding butadiene to the catalyst system. According to thepatent, the propylene content of the copolymer was much higher than that of the copolymer prepared by the catalyst formed after the monomers were mixed. This result is inconsistent with the result described in the above paper. A copolymerizationreaction of butadiene and propylene was also carried out by using a catalyst system of triethylaluminum and titanium tetrachloride prepared in propylene and the product was confirmed, by fractional precipitation test, to be a copolymer of butadiene andpropylene (Chemistry of High Polymers, The Society of Polymer Science, Japan, 20, 461 (1963)). The molar ratio of triethylaluminum to titanium tetrachloride of the above catalyst system was 1.5 (Al/Ti=1.5). The content of this paper corresponds to thatof the above British patent, but there is no description in it showing that the copolymer should be a random copolymer of butadiene and propylene.
According to the methods of British Patent 982,708, a mixture containing 80-95 mole percent butadiene, the rest being 4-methyl-1-pentene, is polymerized at a temperature in the range 0.degree. to 30.degree. C. by a catalyst system which is thereaction product of vanadium (V) oxychloride with triisobutylaluminum, an aluminum-dialkyl monochloride or an aluminum sesquialkyl chloride. The microstructure of the copolymer is not shown in the patent. British Patent 924,654 describes a process forpreparing a copolymer of butadiene and propylene by using an "Alfin" catalyst. The copolymer showed a characteristic infra-red absorption band at 11.95 microns. It was ascribed to trisubstituted ethylene structure. Therefore, the result does notsupport the assumption that the copolymer should be a random or alternating copolymer of butadiene and propylene.
Recently, Furukawa et al. also reported the process of preparing alternating copolymers of butadiene and .alpha.-olefine by using vanadyl (V) chloride-diethylaluminum monochloride-triethylaluminum catalyst system (22nd Annual Meeting of JapanChemical Society, Tokyo, Mar. 31, 1969). However, the molecular weight of the copolymer was very low and its intrinsic viscosity did not exceed 0.1 dl./g.
Consequently, as far as the inventors know, with the exception of the methods of Furukawa et al. described above, there is no prior art in connection with alternating copolymers of butadiene and .alpha.-olefine nor of a process for theirpreparation.
SUMMARY OF THE INVENTION
The object of the present invention is to provide new catalytic systems giving high molecular weight alternating copolymer of butadiene and .alpha.-olefine in high yield.
In accordance with this invention, we have found that by using the catalyst system composed of the first component of an organoaluminum compound having the general formula of AlR.sub.3 where R represents a hydrocarbon radical selected from thegroup consisting of alkyl, aryl and cycloalkyl radicals and at least one R is selected from the group consisting of an alkyl radical having at least 3 carbon atoms, aryl radical and cycloalkyl radical and the second component of titanium tetrahalidehaving the general formula of TiX'.sub.4 (wherein X' represents chlorine, bromine or iodine, hereinafter the same) or by using the catalyst system composed of the first component of AlR.sub.3 wherein R represents a hydrocarbon radical selected from thegroup consisting of alkyl, aryl and cycloalkyl radicals, the second component of TiX'.sub.4 (wherein X' is the same as that defined above) and the third component of a carbonyl group-containing compound, high molecular weight alternating copolymers ofbutadiene and .alpha.-olefine can be produced in high yield. We have also found that by adding halogen (fluorine inclusive), halogen (fluorine inclusive) containing compound, metal oxide or metalloid oxide to the above mentioned catalyst systems, thecatalytic properties of the above mentioned catalysts can be further improved.
The alternating copolymers of this invention are rubber-like in character and can be used as polymeric plasticizers, in adhesives and can be vulcanized with sulfur or a sulfur compound to produce vulcanized elastomers.
The microstructure of butadiene unit of the alternating copolymer of butadiene and .alpha.-olefine prepared by the methods of Furukawa et al. described above was trans 1.4-configuration. The main components forming the catalyst systems were anorganoaluminum compound and a vanadium compound. On the other hand the main components forming the catalyst systems of this invention are an organoaluminum compound and a titanium compound and moreover considerable amounts of cis 1.4-configuration andsmall amounts of 1.2-configuration are found in the butadiene unit of the alternating copolymer. In other words the structure of the alternating copolymer prepared by the catalyst system of an organoaluminum compound and a vanadim compound previouslyreported is different from that of the alternating copolymer prepared by the catalyst system of an organoaluminum compound and a titanium compound of this invention. Therefore the alternating copolymers of butadiene and .alpha.-olefine prepared by theprocess of this invention are new materials.
The carbonyl group containing compound which form the third component of the catalyst systems of this invention are carbon dioxide, aldehyde, keto-aldehyde, ketone, carboxylic acid, keto-carboxylic acid, oxy-carboxylic acid, carboxylic acidhalide, keto-carboxylic acid halide, oxy-carboxylic acid halide, carboxylic acid anhydride, keto-carboxylic acid anhydride, oxy-carboxylic acid anhydride, salt of carboxylic acid, salt of keto-carboxylic acid, salt of oxy-carboxylic acid, ester ofcarboxylic acid, ester of keto-carboxylic acid, ester of oxy-carboxylic acid, carbonyl halide, carbonate, carbonic ester, lactone, ketene, quinone, acyl peroxide, metal complex involving carbonyl group, acid amide, acid imide, isocyanate, aminoacid,urein, ureide, salt of carbamic acid, ester of carbamic acid, ureide acid, etc.
The halogen used as the other third component of the catalyst system of this invention is chlorine, bromine iodine or fluorine. The halogen compounds which form the other third component of the catalyst system of this invention are the compoundshaving transition metal-X linkage (X is halogen) such as compounds having the general formulae VX.sub.4, VOX.sub.3, WX.sub.6, MoX.sub.5, CrO.sub.2 X.sub.2, ZrX.sub.4, FeX.sub.3, OV(OR).sub.n X.sub.3.sub.-n (R is a hydrocarbon radical such as alkylradical, aryl radical or cycloalkyl radical, hereinafter the same, and n is a number from 1 to 2), Zr(OR).sub.2 X.sub.2, Ti(OR).sub.n X.sub.4.sub.-n (n is a number from 1 to 3), Zr(OR).sub.3 X, OV(C.sub.5 H.sub.7 O.sub.2).sub.n X.sub.3.sub.-n (n is anumber from 1 to 2), V(C.sub.5 H.sub.5).sub.n X.sub.4.sub.-n (n is a number from 1 to 2, V(C.sub.5 H.sub.5).sub.2 X, OV(C.sub.5 H.sub.5)X.sub.2, Ti(C.sub.5 H.sub.5).sub.2 X, Ti(C.sub.5 H.sub.5)X.sub.3, Ti(C.sub.5 H.sub.5).sub.2 X.sub.2, (C.sub.5H.sub.5)Ti(OR)X.sub.2, (C.sub.5 H.sub.5).sub.2 CrX, (C.sub.5 H.sub.5)Mo(CO).sub.3 X, (C.sub.5 H.sub.5).sub.2 IrX.sub.3, etc.; and alkane compounds having C-X linkage wherein X is halogen such as tert-butyl chloride, tert-butyl bromide, tert-butyl iodide,sec-butyl chloride, sec-butyl bromide, sec-butyl iodide, carbon tetrachloride, carbon tetrabromide, carbon tetraiodide, etc.; Lewis acid-base complex compounds which formed from halogen compounds showing Lewis acid property such as compounds of thegeneral formulae H.sub.g X.sub.2 (wherein X is halogen, hereinafter the same). CuX, ZnX.sub.2, BiX.sub.3, FeX.sub.3, SnX.sub.4, BX.sub.3, AlX.sub.3, AlR.sub.n X.sub.3.sub.-n (R is a hydrocarbon radical such as alkyl radical, aryl radical or cycloalkylradical, hereinafter the same, and n is a number from 1 to 2), VOX.sub.3, VX.sub.4, CrO.sub.2 X.sub.2, NiX.sub.2, MoX.sub.5, ZrX.sub.4, PX.sub.5, SbX.sub.5, AlOX, WX.sub.6, MnX.sub.2, M.sub.g X.sub.2, and the like. Lewis base such as ether, pyridine,amine, phosphine, derivatives of these compounds, etc., are also employed. The halogen compounds which form the fourth component of the catalyst system of this invention are the ones showing Lewis acid property such as compounds of the general formulaeVX.sub.4 (wherein X is halogen, hereinafter the same), VOX.sub.3, WX.sub.6, MoX.sub.5, CrO.sub.2 X.sub.2, ZrX.sub.4, FeX.sub.3, BX.sub.3, PX.sub.5, SnX.sub.4, SbX.sub.5, AlOX, AlX.sub.3, AlR.sub.n X.sub.3.sub.-n (R is a hydrocarbon radical such as alkylradical, aryl radical or cycloalkyl radical and n is a number from 1 to 2), WX.sub.6, CuX, MnX.sub.2, MgX.sub.2, ZnX.sub.2, HgX.sub.2, BiX.sub.3, NiX.sub.2, etc.; Lewis base complex compounds of the above mentioned halogen compounds showing Lewis acidproperty such as compounds of the general formulae AlX.sub.3 -O(C.sub.2 H.sub.5).sub.2, BX.sub.3 -O(C.sub.2 H.sub.5).sub.2, ZnX.sub.2 -Py (wherein Py represents pyridine, hereinafter the same), VOCl.sub.3 -O(C.sub.2 H.sub.5).sub.2, NiX.sub.2 -Py,FeX.sub.3 -O(C.sub.2 H.sub.5).sub.2, HgX.sub.2 -Py, etc.; organoaluminum compounds having Al-X linkage such as compounds of Al(OR).sub.n X.sub.3.sub.-n (n is a number from 1 to 2), etc., organotransition metal compounds having transition metal-X linkagesuch as compounds of the general formulae OV(OR).sub.n X.sub.3.sub.-n (n is a number from 1 to 2), Ti(OR).sub.n X.sub.4.sub.-n (n is a number from 1 to 3), Zr(OR).sub.2 X.sub.2, Zr(OR).sub.3 X, OV(C.sub.5 H.sub.7 O.sub.2).sub.n X.sub.3.sub.-n (n is anumber from 1 to 2), V(C.sub.5 H.sub.5).sub.n X.sub.4.sub.-n (n is a number from 1 to 2), V(C.sub.5 H.sub.5).sub.2 X, OV(C.sub.5 H.sub.5)X.sub.2, Ti(C.sub.5 H.sub.5).sub.2 X, Ti(C.sub.5 H.sub.5)X.sub.3, Ti(C.sub.5 H.sub.5).sub. 2 X.sub.2, (C.sub.5H.sub.5)Ti(OR)X.sub.2, (C.sub.5 H.sub.5).sub.2 CrX, (C.sub.5 H.sub.5)Mo(CO).sub.3 X, (C.sub.5 H.sub.5).sub.2 IrX.sub.3, etc.; halogenated alkane compounds such as tert-butyl halide, sec-butyl halide, carbon tetrahalide. The metal oxide or metalloidoxide which forms the other fourth component of the catalyst system of the present invention are magnesium oxide, zinc oxide, aluminum oxide, titanium dioxide, vanadium pentoxide, silicon dioxide, silica-alumina, zeolite, boron trioxide, etc.
In the preferred embodiment, the molar ratio of organoaluminum compound which forms the first component of the catalyst system of the present invention to titanium tetrahalide which forms the second component of the catalyst system should behigher than (1.5 Al/Ti>1.5).
The olefine should be one having the general formula:
(in this formula, R' may be a normal chain or branched chain lower alkyl group or a phenyl group).
The preparation of the alternating copolymer of butadiene and .alpha.-olefine is carried out by contacting butadiene with .alpha.-olefine in liquid phase in the presence of the catalyst system described above. The copolymerization reaction isgenerally carried out in the presence of a liquid organic diluent. A suitable diluent that can be used for the copolymerization reaction is a hydrocarbon compound, such as heptane, octane, isooctane, benzene or toluene. The temperature of thecopolymerization reaction may be varied from -100.degree. C. to 50.degree. C. and sufficient pressure is employed to keep the monomers in liquid phase. The molar ratio of butadiene to .alpha.-olefine in the initial monomer composition may be from20:80 to 80:20 and more preferably is 50:50.
At the completion of the copolymerization reaction, the product is precipitated and deashed by using a methanol-hydrochloric acid mixture. The precipitated product is washed with methanol for several times and dried under vacuum. Thereafter theproduct is extracted with methyl ethyl ketone and diethyl ether successively. The methyl ethyl ketone soluble fraction is a low molecular weight alternating copolymer and methyl ethyl ketone insoluble and diethyl ether soluble fraction is a highmolecular weight alternating copolymer.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 shows the infra-red spectrum of the methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and propylene prepared by the process of this invention;
FIG. 2 shows the nuclear magnetic resonance spectrum of the copolymer;
FIG. 3 shows the infra-red spectrum of the methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and 4-methyl pentene-1 prepared by the process of this invention;
FIG. 4 shows the nuclear magnetic resonance spectrum of the copolymer;
FIG. 5 shows the infra-red spectrum of the methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and pentene-1 prepared by the process of this invention;
FIG. 6 shows the nuclear magnetic resonance spectrum of the copolymer;
FIG. 7 shows the infra-red spectrum of the methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and butene-1 prepared by the process of this invention;
FIG. 8 shows the nuclear magnetic resonance spectrum of the copolymer;
FIG. 9 shows the infra-red spectrum of the alternating copolymer of butadiene and styrene prepared by the process of this invention; and
FIG. 10 shows the nuclear magnetic resonance spectrum of the copolymer.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The invention will be illustrated with reference to the following examples.
Example 1
The usual, dry, air-free technique was employed and 6.5 milliliters toluene, 0.50 millimole carbonyl group containing compound and 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) were put successively in a 25milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molarsolution) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed tocopolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 1. As can be seen in Table 1, the yield of high molecular weight alternating copolymer increased by using three components catalyst system.
The following results support the conclusion that the copolymer is an alternating copolymer of butadiene and propylene.
(1) The composition of the copolymer according to the NMR analysis substantially agrees with the calculated value for 1:1 copolymer of butadiene and propylene. Copolymer compositions were determined by measuring the ratio of peak area at4.65.tau. of butadiene unit to that of doublet at 9.11.tau. and 9.20.tau. of propylene unit.
(2) The copolymerization reaction gives 1:1 copolymer over a wide range of initial monomer composition.
(3) The copolymerization reaction gives 1:1 copolymer independently of polymerization time.
(4) The 1155 cm..sup.-.sup.1 band of propylene homopolymer is not shown in its infra-red spectrum. This means at least that the length of the propylene-propylene repeating unit of the copolymer is not so long as to be detected by its infra-redspectrum.
TABLE 1 __________________________________________________________________________ Alternating copolymer MEK insoluble, diethyl ether soluble fraction Catalysts MEK Microstructure of butadiene soluble unit (percent) Experiment Al(i-Bu).sub.3 TiCl.sub.4 fraction Yield No. (mmol) (mmol) Carbonyl compound Mmol (g.) (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 2.0 0.2 1-chloroethyl benzoate 0.50 0.05 0.05 2 2.0 0.2Benzophenone 0.50 0.23 0.57 57 36 7 3 2.0 0.2 Isobutylaldehyde 0.50 0.20 0.57 4 2.0 0.2 Benzoyl chloride 0.50 0.25 0.23 5 2.0 0.2 Isobutyric acid 0.50 0.12 1.39 69 26 5 6 2.0 0.2 Benzoic acid 0.50 0.14 0.61 7 2.0 0.2 Monochloroacetic acid 0.500.17 0.29 8 2.0 0.2 Maleic acid anhydride 0.50 0.16 0.82 70 24 6 Reference 2.0 0.2 0.03 __________________________________________________________________________
Example 2
The usual, dry, air-free technique was employed and 6.5 milliliters toluene, 0.50 millimole carbonyl group containing compound and 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) were put successively in a 25milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molarsolution) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed tocopolymerize at -15.degree. C. for 16 hours. The results are summarized in Table 2.
TABLE 2 __________________________________________________________________________ Alternating copolymer MEK insoluble diethyl ether soluble fraction Catalysts MEK Microstructure of butadiene soluble unit (percent) Experiment Al(i-Bu).sub.3 TiCl.sub.4 fraction Yield No. (mmol) (mmol) Carbonyl compound Mmol (g.) (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 2.0 0.2 Diethyl malonate 0.50 0.35 0.12 74 21 5 2 2.0 0.2Ethyl acetate 0.50 0.30 0.56 60 28 12 3 2.0 0.2 Acetone 0.50 0.62 0.42 65 28 7 4 2.0 0.2 Benzaldehyde 0.50 0.21 0.18 57 35 8 5 2.0 0.2 Acetic acid anhydride 0.50 0.17 1.85 64 30 6 Reference 2.0 0.2 0.07 __________________________________________________________________________
Example 3
The usual, dry, air-free technique was employed and 6.5 milliliters toluene, varying amounts of carbonyl group containing compound and 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) were put successively in a 25milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triethylaluminum solution in toluene (1 molarsolution) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed tocopolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 3.
TABLE 3 __________________________________________________________________________ Alternating copolymer MEK insoluble, diethyl ether soluble fraction Catalysts MEK Microstructure of butadiene soluble unit (percent) Experiment AlEt.sub.3 TiCl.sub.4 fraction Yield No. (mmol) (mmol) Carbonyl compound (g.) (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 2.0 0.2 Maleic acid anhydride 0.05 (g.) 0.11 0.11 57 30 13 2 2.00.2 Propionic acid 0.037 (ml.) 0.21 0.21 70 25 5 Reference 2.0 0.2 0 0 __________________________________________________________________________
Example 4
The usual, dry, air-free technique was employed and 3.5 milliliters toluene, 0.12 milliliter acetic acid anhydride and 0.5 millimole titanium tetrabromide were put in a 25 milliliters glass bottle at 25.degree. C. Then the bottle was left aloneat 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 5.0 milliliters triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 milliliters liquid propylene, 2 millilitersliquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 14 hours. Yield of the methyl ethylketone soluble alternating copolymer of butadiene and propylene was 0.13 g. and that of methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and propylene was 1.67 g. When the two components catalyst systemconsisting of 0.5 millimole titanium tetrabromide and 5.0 millimoles triisobutylaluminum was used and the other copolymerization conditions were the same as the example, yield of the methyl ethyl ketone soluble fraction was 0.07 g. and that of methylethyl ketone insoluble and diethyl ether soluble fraction was 0.03 g.
Example 5
The usual, dry, air-free technique was employed and 3.5 milliliters toluene, 0.12 milliliter isobutyric acid and 0.5 millimole titanium tetraiodide were put successively in a 25 milliliters glass bottle at 25.degree. C. Then the bottle was leftalone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 5.0 milliliters triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 milliliters liquid propylene, 2milliliters liquid butadiene and 2 milliliters toluene, were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 14 hours. Yield of thealternating copolymer was 0.10 g. When the two components catalyst system consisting of 0.5 millimole titanium tetraiodide and 5.0 millimoles triisobutylaluminum was used and the other copolymerization conditions were the same as the example, yield ofthe alternating copolymer was 0.01 g.
Example 6
The usual, dry, air-free technique was employed and varying amounts of carbonyl group containing compound, 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) and 6.5 milliliters toluene were put successively in a 25milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molarsolutions) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual dry, air-free technique. Thereafter the bottle was sealed and allowed tocopolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 4.
TABLE 4 __________________________________________________________________________ Alternating copolymer MEK Insoluble diethyl ether soluble fraction Catalysts MEK Microstructure of butadiene soluble unit (percent) Experiment Al(i-Bu).sub.3 TiCl.sub.4 fraction Yield No. (mmol) (mmol) Carbonyi compound Gram (g.) (g.) Trans- Cls- 1,2- __________________________________________________________________________ 1 2.0 0.2 Sodium oleate 0.152 0.01 0.20 2 2.0 0.2 Aluminumstearate 0.438 0.50 1.30 63 30 7 3 2.0 0.2 Aluminum acetate 0.102 0.01 0.20 75 20 5 4 2.0 0.2 Tin (II) oxalate 0.103 0.05 0.15 74 21 5 5 2.0 0.2 Aluminum acetylacetonate 0.162 0.05 0.22 82 15 3 6 2.0 0.2 Hexacarbonyl molybdenum 0.132 0.050.15 83 14 3 Reference 2.0 0.2 0.03 __________________________________________________________________________
Example 7
The usual, dry, air-free technique was employed and 6.5 milliliters toluene, varying amounts of carbonyl group containing compound and 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) were put successively in a 25milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molarsolution) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed tocopolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 5. In the table, .eta. means the intrinsic viscosity measured in chloroform at 30.degree. C. FIG. 1 shows the infra-red spectrum of the methyl ethyl ketone insolubleand diethyl ether soluble alternating copolymer of butadiene and propylene prepared by the process of Exp. No. 3. FIG. 2 shows the nuclear magnetic resonance spectrum of the copolymer.
TABLE 5 __________________________________________________________________________ Alternating copolymer MEK insoluble, diethyl ether soluble fraction Catalysts MEK Microstructure of butadiene soluble unit (percent) Experiment Al(i-Bu).sub.3 TiCl.sub.4 fraction Yield [.eta.] No. (mmol) (mmol) Carbonyl compound Mmol (g.) (g.) (dl./g.) Trans- Cis- 1,2 __________________________________________________________________________ 1 2.0 0.2 Acetic acid 0.025 0.19 0.08 55 387 2 2.0 0.2 Acetic acid 0.100 0.28 0.21 67 24 9 3 2.0 0.2 Acetic acid 0.500 0.36 0.79 66 29 5 4 2.0 0.2 Acetic acid 0.750 0.13 0.19 66 28 6 5 2.0 0.2 Isobutyl aldehyde 0.250 0.26 0.23 72 22 6 6 2.0 0.2 Isobutyl aldehyde 0.750 0.17 0.44 0.56 65 26 9 7 2.0 0.2 Isobutyl aldehyde 1.000 0.03 0.20 60 32 8 8 2.0 0.2 Acetone 0.750 0.16 0.24 69 25 6 9 2.0 0.2 Benzoyl peroxide 0.500 0.11 0.20 1.40 50 38 12 10 2.0 0.2 Diphenyl acetic acid 0.500 0.21 1.69 0.45 70 24 6 11 2.0 0.2.alpha.-chloropropionic acid 0.500 0.14 0.94 0.36 62 28 10 12 2.0 0.2 Caproic acid 0.500 0.52 0.69 0.33 59 33 8 13 2.0 0.2 Phthalic acid anhydride 0.500 0.17 0.44 0.90 73 19 8 __________________________________________________________________________
Example 8
The usual, dry, air-free technique was employed and 190 milliliters toluene, 0.8 milliliter propionic acid anhydride and 0.275 milliliter titanium tetrachloride were put successively in a 500 milliliters glass bottle at 25.degree. C. Then thebottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 25 milliliters triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 50 milliliters liquidpropylene and 50 milliliters liquid butadiene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 42 hours. 58.0 g. alternatingcopolymer of butadiene and propylene was obtained. Its intrinsic viscosity was 2.26 (dl./g.) in chloroform at 30.degree. C.
The vulcanization was carried out in the following way:
Parts ______________________________________ Copolymer 100 Oil furnace black (HAF) 50 Zinc oxide 5 Sulphur 2 Stearic acid 1 Phenyl-.beta.-naphthyl amine 1 Benzothiazyl disulfide 1 ______________________________________
were mixed on a roller and vulcanized within 60 minutes at 150.degree. C.
The product obtained by the vulcanization had the following values:
Elongation at break at 25.degree. C.: 330%
Tensile strength at 25.degree. C.: 193 kg./cm..sup.2
Modulus 300% at 25.degree. C.: 182 kg./cm..sup.2
The microstructure of butadiene unit of the copolymer was as follows:
trans: 68%
cis: 26%
1.2: 6%
Example 9
The usual, dry, air-free technique was employed and 6.5 milliliters toluene, varying amounts of carbonyl group containing compound and 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) were put successively in a 25milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molarsolution) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed tocopolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 6.
TABLE 6 __________________________________________________________________________ Alternating copolymer MEK Insoluble, diethyl ether soluble fraction Catalysts MEK Microstructure of butadiene soluble unit (percent) Experiment Al(i-Bu).sub.3 TiCl.sub.4 fraction Yield No. (mmol) (mmol) Carbonyl compound Gram (g.) (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 2.0 0.2 Azodicarbonamide 0.06 0.12 0.11 2 2.0 0.2Chloroacetamide 0.047 0.13 0.10 -3 2.0 0.2 Phenylisocyanate .sup.1 0.054 0.19 0.05 4 2.0 0.2 Phenylurethane 0.083 0.24 0.35 61 34 5 5 2.0 0.2 Benzohydroxamic acid 0.07 0.09 0.10 Reference 2.0 0.2 0.03 __________________________________________________________________________ .sup.1 Milliliter.
Example 10
The usual, dry, air-free technique was employed and 7.5 milliliters toluene, 0.1 millimole titanium tetrachloride and varying amounts of carbonyl group containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C.Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and varying amounts of triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 millilitersliquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 21hours. The results are summarized in Table 7.
TABLE 7 __________________________________________________________________________ Alternating copolymer Catalysts Microstructure of butadiene unit (percent) Experiment Al(i-Bu).sub.3 TiCl.sub.4 Yield No. (mmol) (mmol) Carbonyl compound Mmol (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 1.0 0.1 Terephthaldehyde 0.25 0.25 2 1.0 0.1 Glycolic acid 0.25 0.33 3 0.5 0.1 Carbon dioxide 0.25 0.15 4 0.5 0.1 Acetophenone 0.10 1.90 8215 3 5 1.0 0.1 Benzil 0.25 0.25 6 1.0 0.1 Polyvinylacetate .sup.1 0.01 0.17 7 1.0 0.1 Tartaric acid 0.25 0.15 Reference 1 1.0 0.1 0.02 Reference 2 0.5 0.1 0.04 __________________________________________________________________________ .sup.1Gram.
Example 11
The usual, dry, air-free technique was employed and 7.5 milliliters toluene, 0.1 millimole titanium tetrabromide and varying amounts of carbonyl group containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C.Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath and varying amounts of triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 milliliters liquid propylene,2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 21 hours. The resultsare summarized in Table 8.
TABLE 8 __________________________________________________________________________ Alternating copolymer Catalysts Microstructure of butadiene unit (percent) Experiment Al(i-Bu).sub.3 TiBr.sub.4 Yield No. (mmol) (mmol) Carbonyl compound Mmol (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 1.0 0.1 Benzalacetophenone 0.25 0.97 2 1.0 0.1 Diketene 0.25 0.12 3 0.5 0.1 p-Methoxybenzoic acid 0.10 0.57 4 0.5 0.1 p-Benzoquinone 0.100.14 68 25 7 5 0.5 0.1 Polymethylmethacrylate .sup.1 0.01 0.20 Reference 1 1.0 0.1 0.02 Reference 2 0.5 0.1 0.04 __________________________________________________________________________ .sup.1 Gram.
Example 12
The usual, dry, air-free technique was employed and 7.5 milliliters toluene, 0.1 millimole titanium tetrachloride and varying amounts of carbonyl group containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C.Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 1.0 milliliter triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 millilitersliquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16hours. The results are summarized in Table 9.
TABLE 9 __________________________________________________________________________ Alternating copolymer MEK Insoluble, diethyl ether soluble fraction Catalysts MEK Microstructure of butadiene soluble unit (percent) Experiment Al(i-Bu).sub.3 TiCl.sub.4 fraction Yield No. (mmol) (mmol) Carbonyl compound Mmol (g.) (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 1.0 0.1 Phosgene 0.1 0.07 0.24 85 13 2 2 1.0 0.1 Phosgene0.2 0.10 0.17 3 1.0 0.1 Acetyl chloride 0.25 0.18 0.53 4 1.0 0.1 Titanium oxydiacetylacetonate .sup.1 0.05 0.13 0.10 5 1.0 0.1 Zinc carbonate .sup.1 0.05 0.05 0.12 6 1.0 0.1 Sodium carbonate .sup.1 0.05 0.08 0.10 7 1.0 0.1 Dimethyl carbonate 0.1 0.22 0.34 76 19 5 __________________________________________________________________________ .sup.1 Gram.
Example 13
The usual, dry, air-free technique was employed and 7.5 milliliters toluene, 0.2 milliliter titanium tetrachloride and 0.5 millimole carbonyl group containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C. Thenthe bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 milliliters liquidpropylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 10.
TABLE 10 __________________________________________________________________________ Alternating copolymer MEK insoluble, diethyl ether soluble fraction Catalysts MEK Microstructure of butadiene soluble unit (percent) Experiment Al(i-Bu).sub.3 TiCl.sub.4 fraction Yield No. (mmol) (mmol) Carbonyl compound Mmol (g.) (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 2.0 0.2 Trimethyl acetic acid 0.5 0.42 0.56 2 2.0 0.2Crotonic acid 0.5 0.20 0.35 68 28 4 3 2.0 0.2 Trichloro acetic acid 0.5 0.03 0.18 4 2.0 0.2 Isobutyric acid anhydride 0.5 0.14 1.29 65 29 6 5 2.0 0.2 Crotonic acid anhydride 0.5 0.04 0.57 72 23 5 6 2.0 0.2 Benzoic acid anhydride 0.5 0.10 0.80 72.0 0.2 n-Butyric acid 0.5 0.62 0.80 66 29 7 __________________________________________________________________________
Example 14
The usual, dry, air-free technique was employed and 7.0 milliliters toluene, 0.1 millimole titanium tetrachloride and varying amounts of carbonyl group containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C.Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and varying amounts of triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 millilitersliquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize for 16 hours at 0.degree. C. or -55.degree. C. The results are summarized in Table 11.
TABLE 11 __________________________________________________________________________ Alternating copolymer MEK insoluble, diethyl ether soluble fraction Microstructure of Catalysts Polymer- MEK butadiene unit Exper- ization soluble (percent) iment Al(i-Bu).sub.3 TiCl.sub.4 tempera- fraction Yield No. (mmol) (mmol) Carbonyl compound Mmol ture (.degree.C.) (g.) (g.) Trans- Cis- 1,2 __________________________________________________________________________ 1 0.5 0.1Acetophenone 0.1 -55 0.02 0.27 88 8 4 2 0.5 0.1 Acetophenone 0.1 0 0.16 0.29 70 23 7 3 0.5 0.1 Isobutyl aldehyde 0.1 -55 0.01 0.29 76 20 4 4 0.5 0.1 Isobutyl aldehyde 0.1 0 0.14 0.20 62 28 10 5 1.0 0.1 Propionic acid anhydride 0.25 -55 0.01 0.1381 16 3 6 1.0 0.1 Propionic acid anhydride 0.25 0 0.06 1.14 69 27 4 __________________________________________________________________________
Example 15
The usual, dry, air-free technique was employed and varying amounts of carbonyl group containing compound, 6.5 milliliters toluene and varying amounts of titanium tetrachloride were put successively in a 25 milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 millilitersliquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16hours. The results are summarized in Table 12.
TABLE 12 __________________________________________________________________________ Alternating copolymer MEK insoluble, diethyl ether soluble fraction Microstructure of Catalysts MEK butadiene unit soluble (percent) Experi- Al(i-Bu).sub.3 TiCl.sub.4 fraction Yield ment No. (mmol) (mmol) Carbonyl compound* Mmol. (g.) (g.) Trans- Cis- 1,2- __________________________________________________________________________ 1 2.0 0.2 O 0.16 0.18 0.06 66 28 6 .parallel. TiCl.sub.3 (OCCH.sub.3) 2 2.0 0.5 O 0.20 0.17 0.15 .parallel. Ti(Oi--Pr).sub.2 (OCCH.sub.3).sub.3 3 2.0 0.5 O 0.20 0.32 1.71 63 32 5 .parallel. O[Ti(OCCH.sub.3).sub.3 ].sub.3 __________________________________________________________________________ *i-Pr=Isopropyl; i-Bu=Isobutyl.
Example 16
The usual, dry, air-free technique was employed and 7.0 milliliters toluene, 0.1 millimole titanium tetrachloride and varying amounts of carbonyl containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C. Thenthe bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and varying amounts of organoaluminum solution in toluene (1 molar solution), 2 milliliters liquid butadiene and 3.1milliliters liquid 4-methyl pentene-1 were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16 hours. The results are summarized inTable 13.
The following results support the conclusion that the copolymer is an alternating copolymer of butadiene and 4-methyl pentene-1.
(1) The composition of the copolymer according to the NMR analysis substantially agrees with the calculated value for the 1:1 copolymer of butadiene and 4-methyl pentene-1.
(2) The copolymerization reaction gives 1:1 copolymer over a wide range of initial monomer composition.
(3) The copolymerization reaction gives 1:1 copolymer independently of polymerization time.
TABLE 13 __________________________________________________________________________ Alternating copolymer Catalysts MEK MEK insolu- Organo- soluble ble, diethyl Experiment aluminum TiCl.sub.4 fraction ether soluble No. compound* Mmol (mmol) Carbonyl compound Mmol (g.) fraction (g.) __________________________________________________________________________ 1 AlEt.sub. 3 0.5 0.1 Isobutyl aldehyde 0.10 0.02 0.03 2 AlEt.sub.3 1.0 0.1 Propionic acid anhydride 0.25 0.05 0.26 3Al(i-Bu).sub.3 1.0 0.1 Propionic acid anhydride 0.25 0.03 0.87 4 Al(i-Bu).sub.3 0.5 0.1 Acetophenone 0.10 0.06 1.05 5 Al(i-Bu).sub.3 0.5 0.1 Acetone 0.10 0.05 0.31 6 Al(i-Bu).sub.3 1.0 0.1 Acetic acid 0.25 0.11 0.32 7 Al(i-Bu).sub.3 0.5 0.10.02 Reference AlEt.sub.3 0.5 0.1 0 __________________________________________________________________________ *Et=Ethyl; i-Bu=Isobutyl.
FIG. 3 shows the infra-red spectrum of the methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and 4-methyl-pentene-1 prepared by the process of Exp. No. 4. FIG. 4 shows the nuclear magnetic resonancespectrum of the copolymer.
Example 17
The usual, dry, air-free technique was employed and 7.0 milliliters toluene, 0.1 millimole titanium tetrahalide and varying amounts of carbonyl group containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C.Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and varying amounts of organoaluminum solution in toluene (1 molar solution), 2 milliliters liquid butadiene and2.8 milliliters liquid pentene-1 were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16 hours. The results are summarized in Table14.
The following results support the conclusion that the copolymer is an alternating copolymer of butadiene and pentene-1.
(1) The composition of the copolymer according to the NMR analysis substantially agrees with the calculated value for the 1:1 copolymer of butadiene and pentene-1.
(2) The copolymerization reaction gives 1:1 copolymer over a wide range of initial monomer composition.
(3) The copolymerization reaction gives 1:1 copolymer independently of polymerization time.
TABLE 14 __________________________________________________________________________ Catalysts Alternating copolymer MEK MEK insoluble, Organo- soluble diethyl ether Experiment aluminum Titanium fraction soluble No. compound* Mmol tetrahalide Mmol Carbonyl compound Mmol (g.) fraction __________________________________________________________________________ (g.) 1 AlEt.sub.3 0.5 TiCl.sub.4 0.1 Acetophenone 0.10 0.03 0.06 2 Al(i-Bu).sub.3 0.5 TiCl.sub.4 0.1 " 0.10 0.061.02 3 Al(i-Bu).sub.3 0.5 TiCl.sub.4 0.1 Isobutylaldehyde 0.10 0.03 0.43 4 Al(i-Bu).sub.3 0.5 TiBr.sub.4 0.1 " 0.10 0.01 0.13 5 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 Acetic acid 0.25 0.08 0.49 6 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 O 0.02 0.080.11 .parallel. TiCl.sub.3 (OCCH.sub.3) 7 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 Same as above 0.10 0.17 0.84 8 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 Propionic acid anhydride 0.25 0.01 0.17 9 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 Isobutyric anhydride 0.25 0.02 0.19 10 Al(i-Bu).sub.3 1.0 TiCl.sub. 4 0.1 Acetone 0.10 0.02 0.76 11 Al(i-Bu).sub.3 0.5 TiCl.sub.4 0.1 0.08 Reference AlEt.sub.3 0.5 TiCl.sub.4 0.1 0.02 __________________________________________________________________________*Et=Ethyl; i-Bu=Isobutyl.
FIG. 5 shows the infra-red spectrum of the methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and pentene-1 prepared by the process of Exp. No. 5. FIG. 6 shows the nuclear magnetic resonance spectrum ofthe copolymer.
Example 18
The usual, dry, air-free technique was employed and 7.0 milliliters, 0.1 millimole titanium tetrahalide and varying amounts of carbonyl group containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C. Then thebottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and varying amounts or organoaluminum compound in toluene (1 molar solution), 2 milliliters liquid butadiene and 2milliliters liquid butene-1 were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 15.
The following results support the conclusion that the copolymer is an alternating copolymer of butadiene and butene-1.
(1) The composition of the copolymer according to the NMR analysis substantially agrees with the calculated value for the 1:1 copolymer of butadiene and butene-1.
(2) The copolymerization reaction gives 1:1 copolymer over a wide range of initial monomer composition.
(3) The copolymerization reaction gives 1:1 copolymer independently of polymerization time.
TABLE 15 __________________________________________________________________________ Catalysts Alternating copolymer MEK MEK insoluble, Organo- soluble diethyl ether Experiment aluminum Titanium fraction soluble No. compound* Mmol tetrahalide Mmol Carbonyl compound Mmol (g.) fraction __________________________________________________________________________ (g.) 1 AlEt.sub.3 0.5 TiCl.sub.4 0.1 Acetophenone 0.10 0.06 0.15 2 Al(i-Bu).sub.3 0.5 TiCl.sub.4 0.1 Isobutylaldehyde 0.10 0.06 0.26 3 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 Isoamyl acetate 0.25 0.04 0.14 4 Al(i-Bu).sub.3 0.5 TiCl.sub.4 0.1 Benzophenone 0.10 0.04 0.70 5 Al(i-Bu).sub.3 1.0 TiBr.sub.4 0.1 Acetic acid 0.25 0.08 0.11 6 Al(i-Bu).sub.3 1.0 TiBr.sub.4 0.1 Acetone 0.25 0.03 0.05 7 Al(i-Bu).sub.3 0.5 TiBr.sub.4 0.1 Acetophenone 0.10 0.05 1.26 8 Al(i-Bu).sub.3 0.5 TiCl.sub.4 0.1 0.03 Reference AlEt.sub. 3 0.5 TiCl.sub.4 0.1 0 __________________________________________________________________________ *Et=Ethyl; i-Bu=Isobutyl.
FIG. 7 shows the infra-red spectrum of the methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and butene-1 prepared by the process of Exp. No. 4. FIG. 8 shows the nuclear magnetic resonance spectrum ofthe copolymer.
Example 19
The usual, dry, air-free technique was employed and 5.0 milliliters toluene, 0.1 millimole titanium tetrahalide and varying amounts of carbonyl group containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C.Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and varying amounts of organoaluminum solution in toluene (1 molar solution), 3 milliliters styrene and 2milliliters liquid butadiene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 21 hours. The results are summarized in Table 16.
The following results support the conclusion that the copolymer is an alternating copolymer of butadiene and styrene.
(1) The composition of the copolymer according to the NMR analysis substantially agrees with the calculated value for the 1:1 copolymer of butadiene and styrene.
(2) The copolymerization reaction gives 1:1 copolymer over a wide range of initial monomer composition.
(3) The copolymerization reaction gives 1:1 copolymer independently of polymerization time.
TABLE 16 __________________________________________________________________________ Catalysts Organo- Alternating Experiment aluminum Titanium copolymer No. compound* Mmol tetrahalide Mmol Carbonyl compound Mmol (g.) __________________________________________________________________________ 1 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 0.03 2 Al(i-Bu).sub.3 0.5 TiCl.sub.4 0.1 Acetic acid 0.10 0.05 3 Al(i-Bu).sub.3 0.5 TiCl.sub.4 0.1 Propionic acid anhydride 0.10 0.05 4 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 " 0.25 0.25 5 Al(i-Bu).sub.3 0.5 TiBr.sub.4 0.1 p-Benzoquinone 0.10 0.07 6 Al(i-Bu).sub.3 0.5 TiBr.sub.4 0.1 Terephthal aldehyde 0.10 0.11 7 AlEt.sub. 3 0.5 TiBr.sub.4 0.1 Propionic acid anhydride 0.10 0.04 8 Al(i-Bu).sub.3 1.0 TiCl.sub.4 0.1 O 0.10 0.38 .parallel. TiCl.sub.3 (OCCH.sub.3) Reference AlEt.sub.3 0.5 TiCl.sub.4 0.1 0 __________________________________________________________________________ *Et=Ethyl; i-Bu=Isobutyl.
FIG. 9 shows the infra-red spectrum of the alternating copolymer of butadiene and styrene prepared by the process of Exp. No. 8. FIG. 10 shows the nuclear magnetic resonance spectrum of the copolymer.
Example 20
The usual, dry, air-free technique was employed and 4.0 milliliters toluene, 0.2 millimole titanium tetrachloride and 0.2 millimole carbonyl containing compound were put successively in a 25 milliliters glass bottle at 25.degree. C. Then thebottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and varying amounts of triisobutylaluminum solution in toluene (1 molar solution) and 6 milliliters liquid B--B fractionwere put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 24 hours. Alternating copolymer of butadiene and butene-1 was obtained. Theresults are summarized in Table 17. The mole fraction of B--B fraction used was as follows:
Mole percent ______________________________________ Propane 0.03 Propylene 0.05 Methyl acetylene 0.69 Isobutane 0.52 n-Butane 3.67 Isobutylene 26.22 Butene-1 14.18 Trans-butene-2 5.18 Cis-butene-2 4.12 1,3-butadiene 44.02 1,2-butadiene 0.52 Ethyl acetylene 0.16 Vinyl acetylene 0.64 ______________________________________
TABLE 17 __________________________________________________________________________ Alternating copolymer Catalysts MEK MEK insolu- soluble ble, diethyl Experiment Al(i-Bu).sub.3 TiCl.sub.4 Carbonyl fraction ether soluble No. (mmol)(mmol) compound Mmol (g.) fraction (g.) __________________________________________________________________________ 1 1.0 0.2 Acetophenone 0.2 0.14 0.02 2 2.0 0.2 O 0.2 0.16 0.56 .parallel. TiCl.sub. 3 OCCH.sub.3 __________________________________________________________________________
Example 21
The usual, dry, air-free technique was employed and 7.0 milliliters toluene, 1.0 milliliter triisobutylaluminum solution in toluene (1 molar solution), 0.25 millimole propionic acid anhydride, 0.1 millimole titanium tetrachloride and a mixture of2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into a 25 milliliters glass bottle at -78.degree. C. Then the bottle was sealed and allowed to copolymerize at -30.degree. C. for 15 hours. The yield of the alternating copolymer of butadiene and propylene was 0.13 g.
Example 22
The usual, dry, air-free technique was employed and 1.0 millimole butadiene, 0.25 millimole propionic acid anhydride and 0.1 millimole titanium tetrachloride were put successively into a 25 milliliters glass bottle at 25.degree. C. Then thebottle was held in a low temperature bath at -78.degree. C. and 10 milliliters triisobutylaluminum solution in toluene (1 mole solution) and a mixture of 3 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were putsuccessively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 15 hours. The yield of the alternating copolymer of butadiene and propylene was 0.65 g.and the microstructure of butadiene unit of the copolymer was as follows:
trans: 70%
cis: 22%
1,2: 8%
Example 23
The usual, dry, air-free technique was employed and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene, 0.18 millimole titanium tetrachloride, 0.6 milliliter of triisobutylaluminum solution intoluene (1 molar solution) and 0.12 millimole acetophenone were put successively at intervals of 10 minutes into a 25 milliliters glass bottle at -78.degree. C. Thereafter the bottle was sealed and allowed to copolymerize at -40.degree. C. for 4.5hours. The yield of the alternating copolymer of butadiene and propylene was 0.60 g. and the microstructure of butadiene unit of the copolymer was as follows:
trans: 92%
cis: 6%
1.2: 2%
Example 24
The usual, dry, air-free technique was employed and a mixture of 2 milliliters liquid propylene, 2-milliliters liquid butadiene and 2 milliliters toluene, 0.18 millimole titanium tetrachloride, 0.12 millimole acetophenone and 0.6 millilitertriisobutylaluminum solution in toluene (1 molar solution) were put successively at intervals of 10 minutes into a 25 milliliters glass bottle at -78.degree. C. Thereafter the bottle was sealed and allowed to copolymerize at -40.degree. C. for 4.5hours. The yield of the alternating copolymer of butadiene and propylene was 1.05 g. and the microstructure of butadiene unit of the copolymer was as follows:
trans: 91%
cis: 7%
1.2: 2%
Example 25
The usual, dry, air-free technique was employed and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene, 0.6 milliliter triisobutylaluminum solution in toluene (1 molar solution), 0.12 millimoleacetophenone and 0.18 millimole titanium tetrachloride were put successively at intervals of 10 minutes into a 25 milliliters glass bottle at -78.degree. C. Thereafter the bottle was sealed and allowed to polymerize at -40.degree. C. for 4.5 hours. The yield of the alternating copolymer of butadiene and propylene was 1.01 g.
Example 26
The usual, dry, air-free technique was employed and a mixture of 2 milliliters liquid propylene, 2 milliliters toluene, 0.12 millimole acetophenone, 0.18 millimole titanium tetrachloride and 0.6 milliliter triisobutylaluminum solution in toluene(1 molar solution) were put successively at intervals of 10 minutes into a 25 milliliters glass bottle at -78.degree. C. Thereafter the bottle was sealed and allowed to copolymerize at -40.degree. C. for 4.5 hours. The yield of the alternatingcopolymer of butadiene and propylene was 1.06 g.
Example 27
The usual, dry, air-free technique was employed and 0.05 g. metal oxide or metalloid oxide, 6.5 milliliters toluene, 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) and 0.5 millimole carbonyl group containing compoundwere put successively in a 25 milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminumsolution in toluene (1 molar solution) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter thebottle was sealed and allowed to copolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 18. As can be seen in Table 18, the yield of the high molecular weight alternating copolymer of butadiene and propylene increased byadding metal oxide or metalloid oxide to the three components catalyst system of organoaluminum compound, titanium tetrahalide and carbonyl compound.
TABLE 18 __________________________________________________________________________ Alternating copolymer Catalysts MEK MEK insolu- soluble ble, diethyl Experiment Al(i-Bu).sub.3 TiCl.sub.4 Metal oxide or fraction ether soluble No.(mmol) (mmol) Carbonyl compound Mmol metalloid oxide Gram (g.) fraction __________________________________________________________________________ (g.) 1 2.0 0.2 Monochloroacetic acid 0.5 Titanium dioxide 0.05 0.23 *0.82 Reference 1 2.0 0.2 "0.5 0.17 0.20 2 2.0 0.2 Ethyl acetate 0.5 Alumina 0.05 0.17 0.48 Reference 2 2.0 0.2 " 0.5 0.09 0.14 3 2.0 0.2 " 0.5 Vanadium pentoxide 0.05 0.23 0.56 4 2.0 0.2 Diethyl malonate 0.5 Silica 0.05 0.22 0.15 Reference 3 2.0 0.2 " 0.5 0.08 0.04 5 2.0 0.2 Benzophenone 0.5 Zirconium dioxide 0.05 1.48 0.67 Reference 4 2.0 0.2 " 0.5 0.23 0.47 6 2.0 0.2 Acetone 0.5 Titanium dioxide 0.05 0.24 0.22 Reference 5 2.0 0.2 " 0.5 0.24 0.13 7 2.0 0.2 Acetic acid anhydride 0.5 Magnesia 0.05 0.120.93 Reference 6 2.0 0.2 " 0.5 0.13 0.83 __________________________________________________________________________ *Butadiene microstructure: Trans=73%, Cis=12%; 1.2=5%.
Example 28
The usual, dry, air-free technique was employed and 6.0 milliliters toluene, 0.5 millimole carbonyl group containing compound, 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) and 0.2 millimole halogen or halogencompound were put successviely in a 25 milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter, the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliterstriisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 19.
As can be seen in Table 19, the yield of the high molecular weight alternating copolymer of butadiene and propylene was increased by adding halogen or halogen compound to the three components catalyst system of organoaluminum compound, titaniumtetrachloride and carbonyl compound.
TABLE 19 __________________________________________________________________________ Catalysts Alternating copolymer MEK MEK insoluble, soluble diethyl ether Experiment Al(i-Bu).sub.3 TiCl.sub.4 Carbonyl Halogen or halogen com- fraction soluble frac- No. (mmol) (mmol) compound Mmol pound Mmol (g.) tion __________________________________________________________________________ (g.) 1 2.0 0.2 Benzophenone 0.5 Stannic chloride 0.2 0.16 0.79 Reference 1 2.0 0.2 " 0.5 0.23 0.57 22.0 0.2 Benzoyl peroxide 0.5 tert-Butyl chloride 0.2 0.12 0.25 Reference 2 2.0 0.2 " 0.5 0.11 0.20 3 2.0 0.2 Ethyl acetate 0.5 Ethylaluminum dichlo- 0.2 0.10 *0.54 ride. Reference 3 2.0 0.2 " 0.5 0.09 0.14 4 2.0 0.2 Diethyl malonate 0.5Aluminum bromide 0.2 0.09 0.13 Reference 4 2.0 0.2 " 0.5 0.08 0.04 5 2.0 0.2 Acetone 0.5 AlCl.sub.3.O(C.sub.2 H.sub.5).sub.3 0.2 0.18 0.40 Reference 5 2.0 0.2 " 0.5 0.24 0.13 6 2.0 0.2 Benzophenone 0.5 Iodine 0.2 0.15 0.67 __________________________________________________________________________ *Butadiene microstructure: Trans=67%; Cis=25%; 1.2=8%.
Example 29
The usual, dry, air-free technique was employed and 6.0 milliliters toluene, 0.5 millimole isobutyl aldehyde,
TABLE 20 __________________________________________________________________________ Alternating copolymer Catalysts MEK MEK in- Organo- Diluent soluble soluble, diethyl Experiment aluminum TiCl.sub.4 toluene fraction ether soluble No.compound Mmol (mmol) Halogen or halogen compound Mmol. (ml.) (g.) fraction __________________________________________________________________________ (g.) 1 Al(i-Bu).sub.3 2.5 1.0 5 0 0.09 2 Al(i-Bu).sub.3 2.5 1.0 Chromium (VI) oxychloride 1.2 5 0.40 1.00 3 Al(i-Bu).sub.3 2.5 1.0 Vanadium (V) oxychloride 1.0 4 0.89 0.58 4 Al(i-Bu).sub.3 2.5 1.0 tert-Butyl chloride 2.5 5 0.10 0.14 5 Al(i-Bu).sub.3 2.5 1.0 Bromine 0.8 5 0.08 0.34 Reference 1 Al(i-Bu).sub.3 1.5 1.0 5 0 0 Reference2 AlEt.sub.3 2.5 1.0 5 0 0 Reference 3 AlEt.sub.3 1.5 1.0 5 0 0 __________________________________________________________________________
0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) and 0.2 millimole boron trifluoride diethyl ester complex were put successively in a 25 milliliters glass bottle at 25.degree. C. Then the bottle was left alone at100.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2 milliliters liquid butadiene and 2 milliliterstoluene were put successively into the bottle also employing the conventional, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16 hours. The yield of methyl ethyl ketone soluble alternatingcopolymer of butadiene and propylene was 0.18 g. and that of methyl ethyl ketone insoluble and diethyl ether soluble fraction, i.e. alternating copolymer of butadiene and propylene was 0.74 g. When the three components catalyst system consisting oftriisobutylaluminum, titanium tetrachloride and isobutylaldehyde was used and the other copolymerization conditions were the same as those in this example, the yield of the high molecular weight alternating copolymer was 0.47 g.
Example 30
The usual, dry, air-free technique was employed and varying amounts of toluene, 1.0 milliliter titanium tetrachloride solution in toluene (1 molar solution) and varying amounts of halogen or halogen compound were put successively in a 25milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and varying amounts of organoaluminum compound in toluene (1 molarsolution) and a mixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed tocopolymerize at -30.degree. C. for 16 hours. The results are summarized in Table 20. As can be seen in Table 20, by adding halogen or halogen compound to the two components catalyst system consisting of organoaluminum compound and titaniumtetrahalide, the yield of the alternating copolymer increased, Ref. 1 also shows that when the mol ratio of triisobutylaluminum to titanium tetrachloride is 1.5 (Al/Ti=1.5) no alternating copolymer can be obtained.
Example 31
The conventional, dry, air-free technique was employed and 5.0 milliliters toluene, 1.0 milliliter titanium tetrachloride solution in toluene (1 molar solution) and 1.2 millimoles chromium (VI) oxychloride were put successively in a 25 milliliterglass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.5 milliliters triisobutylaluminum solution in toluene (1 molar solution), 3milliliters styrene and 2 milliliters liquid butadiene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 16 hours. The yield ofalternating copolymer of butadiene and styrene was 0.53 g.
Example 32
The usual, dry, air-free technique was employed and 0.5 millimole halogen compound, 6.5 milliliters toluene and 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) were put successively in a 25 milliliter glass bottle at25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2milliliters liquid propylene, milliliters liquid butadiene and 2 milliliters liquid toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at-30.degree. C. for 16 hours. The results are summarized in Table 21.
TABLE 21 __________________________________________________________________________ Catalysts Alternating copolymer MEK MEK insoluble soluble diethyl ether Experiment Al(i-Bu).sub.3 TiCl.sub.4 Halogen fraction soluble fraction No.(mmol) (mmol) compound* Mmol (g.) (g.) __________________________________________________________________________ 1 2.0 0.2 BF.sub.3.OEt.sub.2 0.5 0.12 0.28 2 2.0 0.2 AlCl.sub.3.OEt.sub.2 0.5 0.07 0.12 3 2.0 0.2 ZnCl.sub.2.Py 0.5 0.10 0.08 42.0 0.2 VOCl.sub.3.OEt.sub.2 0.5 0.50 0.60 5 2.0 0.2 NH.sub.2.Py 0.5 0.05 0.15 6 2.0 0.2 FeCl.sub.3.OEt.sub.2 0.5 0.11 0.21 7 2.0 0.1 HgCl.sub.2.Py 0.5 0.05 0.11 8 2.0 0.1 Cu.sub.2 Cl.sub.2.Py 0.5 0.04 0.12 Reference 2.0 0.1 0 0.03 __________________________________________________________________________ *Et=Ethyl; Py=Pyridine.
Example 33
The usual, dry, air-free technique was employed and 0.5 millimole halogen compound, 6.5 milliliters toluene and 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) were put successively in a 25 milliliter glass bottle at25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triisobutylaluminum solution in toluene (1 molar solution) and a mixture of 2milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at -30.degree. C. for 39 hours. The results are summarized in Table 22.
TABLE 22 __________________________________________________________________________ Catalysts Alternating copolymer MEK MEK insoluble Experiment Al(i-Bu).sub.3 TiCl.sub.4 Halogen soluble diethyl ether No. (mmol) (mmol) compound* Mmol fraction soluble fraction (g.) __________________________________________________________________________ 1 2 0.2 BiCl.sub.3.CEt.sub.3 0.5 0.16 0.52 2 2 0.2 SnCl.sub.4.OEt.sub.3 0.5 0.02 0.15 3 2 0.2 BCl.sub.3.OEt.sub.3 0.5 0.02 0.10 Reference 2 0.2 0 0.05 __________________________________________________________________________ *Et=Ethyl.
Example 34
The usual, dry air-free technique was employed and 0.5 millimole bismuth (III) chloride diethyl ether complex, 6.5 milliliters toluene and 0.2 milliliter titanium tetrachloride solution in toluene (1 molar solution) were put successively in a 25milliliters glass bottle at 25.degree. C. Then the bottle was left alone at 25.degree. C. for 10 minutes. Thereafter the bottle was held in a low temperature bath at -78.degree. C. and 2.0 milliliters triethylaluminum solution in toluene and amixture of 2 milliliters liquid propylene, 2 milliliters liquid butadiene and 2 milliliters toluene were put successively into the bottle also employing the usual, dry, air-free technique. Thereafter the bottle was sealed and allowed to copolymerize at-30.degree. C. for 16 hours. The yield of methyl ethyl ketone soluble alternating copolymer of butadiene and propylene was 0.05 g. and methyl ethyl ketone insoluble and diethyl ether soluble alternating copolymer of butadiene and propylene was 0.11 g.By using two components catalyst system of triethylaluminum and titanium tetrachloride, no alternating copolymer of butadiene and propylene was obtained.
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