Claims
- 1. A prepolymerization process for producing a conjugated diene compound prepolymer solution useful for the production of a vinyl aromatic compound high impact polymer material, comprising the steps of:
- preparing a prepolymerization mixture comprising 1 to 70 parts by weight of at least one conjugated diene compound and 30 to 99 parts by weight of at least one vinyl aromatic compound; and
- subjecting the prepolymerization mixture to prepolymerization at a temperature of 0.degree. C. to 150.degree. C. in the presence of a prepolymerization catalyst (A) consisting essentially of:
- mixtures of a component (a) consisting of at least one member selected from the group consisting of organic and inorganic phosphates and of rare earth elements, with a component (b) consisting of at least one organic aluminum compound and a component (c) consisting of at least one Lewis acid, said catalyst causing the conjugated diene compound to be selectively polymerized but is substantially not effective in the polymerization of the vinyl aromatic compound, such that the conjugated diene compound and the vinyl aromatic compound are prepolymerized at degrees of conversion of at least 70 molar % and 10 molar % or less, respectively.
- 2. The prepolymerization process as claimed in claim 1, wherein, in component (a) of prepolymerization catalyst (A), the rare earth element is selected from the group consisting of cerium, lanthanum, praseodymium, neodymium and gadolinium.
- 3. The prepolymerization process as claimed in claim 1, wherein the component (b) of prepolymerization catalyst (A) consists of at least one organic aluminum compound represented by the general formula (I):
- Al R.sub.3-n H.sub.n (I)
- wherein n represents 0, 1 or 2 and R represents a hydrocarbon radical having 1 to 8 carbon atoms.
- 4. The prepolymerization process as claimed in claim 1, wherein the Lewis acid in the component (c) of prepolymerization catalyst (A) is a halogen-containing Lewis acid.
- 5. The prepolymerization process as claimed in claim 4, wherein prepolymerization catalyst (A) has a molar ratio of the component (c) in terms of halogen to the component (a) in terms of the rare earth element, of 2:1 to 6:1.
- 6. The prepolymerization process as claimed in claim 1, wherein prepolymerization catalyst (A) consists essentially of a mixture of a reaction product of the component (a) with the component (b), with the component (c).
- 7. The prepolymerization process as claimed in claim 1, wherein prepolymerization catalyst (A) is present in an amount of 0.5.times.10.sup.-3 moles or less in terms of the rare earth element per 100 g of the conjugated diene compound.
- 8. The prepolymerization process as claimed in claim 1, wherein in prepolymerization catalyst (A), the components (b) and (c) are present in amounts of 2 to 100 molar parts in terms of aluminum and 2 to 6 molar parts in terms of the halogen element, respectively, per one molar part in terms of the rare earth element, of the component (a).
- 9. The prepolymerization process as claimed in claim 6, wherein the reaction product of the component (a) with the component (b) was prepared at a reaction temperature of 0.degree. C. to 100.degree. C.
- 10. The prepolymerization process as claimed in claim 1, wherein the component (a) is reacted with the component (b) and the resultant reaction product is aged in the presence of the conjugated diene compound at a temperature of from 0.degree. C. to 100.degree. C., before the prepolymerization procedure.
- 11. The prepolymerization process as claimed in claim 1, wherein the mixture of prepolymerization catalyst (A) further includes a medium of at least one inert solvent.
- 12. The prepolymerization process as claimed in claim 11, wherein the inert solvent is selected from the group consisting of liquid aliphatic hydrocarbons, cycloaliphatic hydrocarbons and aromatic hydrocarbons.
- 13. The prepolymerization process as claimed in claim 11, wherein the inert solvent medium is present in an amount of 200 parts by weight or less per 100 parts by weight of the total amount of the conjugated diene compound and the vinyl aromatic compound.
- 14. The prepolymerization process as claimed in claim 1, wherein the conjugated diene compound is selected from the group consisting of 1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene and 1,3-hexadiene.
- 15. The prepolymerization process as claimed in claim 1, wherein the vinyl aromatic compound is selected from the group consisting of styrene, o-methylstyrene, p-methylstyrene, p-tert-butylstyrene, 1,3-dimethylstyrene, .alpha.-methylstyrene, vinylnaphthalene and vinylanthracene.
- 16. A process for producing a vinyl aromatic compound high impact polymer material, comprising the steps of:
- preparing a prepolymerization mixture comprising 1 to 70 parts by weight of at least one conjugated diene compound and 30 to 99 parts by weight of at least one vinyl aromatic compound;
- subjecting the prepolymerization mixture to prepolymerization at a temperature of 0.degree. C. to 150.degree. C. in the presence of a prepolymerization catalyst (A) consisting essentially of:
- mixtures of a component (a) consisting of at least one member selected from the group consisting of organic and inorganic phosphates and phosphites of rare earth elements, with a component (b) consisting of at least one organic aluminum compound and a component (c) consisting of at least one Lewis acid, said catalyst causing the conjugated diene compound to be selectively polymerized but is substantially not effective in the polymerization of the vinyl aromatic compound, such that the conjugated diene compound and the vinyl aromatic compound are prepolymerized to degrees of conversion of at least 70 molar % and 10 molar % or less, respectively, resulting in forming a conjugated diene compound prepolymer solution; and
- further subjecting the resultant prepolymer solution to a polymerization procedure in which the remaining vinyl aromatic compound in the solution is polymerized with the conjugated diene compound prepolymer.
- 17. The process as claimed in claim 16, wherein the polymerization is carried out by a radical polymerization method.
- 18. The process as claimed in claim 17, wherein the radical polymerization is non-catalytically carried out by the radical polymerization method at a temperature of 50.degree. C. to 250.degree. C.
- 19. The process as claimed in claim 17, wherein the polymerization is carried out by the radical polymerization method in the presence of a radical polymerization initiator at a temperature of 20.degree. C. to 200.degree. C.
- 20. The process as claimed in claim 17, wherein the radical polymerization is carried out by a bulk polymerization method.
- 21. The process as claimed in claim 17, wherein the radical polymerization is carried out by a bulk-suspension polymerization method in which the vinyl aromatic compound is polymerized by the bulk polymerization method until the degree of conversion of the vinyl aromatic compound reaches a level of 5 to 50 molar% and then by the suspension polymerization method in the presence of a suspension stabilizer.
- 22. The process as claimed in claim 16, wherein the polymerization is carried out by a catalytical anionic polymerization method at a temperature of 20.degree. C. to 180.degree. C.
Priority Claims (2)
Number |
Date |
Country |
Kind |
62-204277 |
Aug 1987 |
JPX |
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62-204278 |
Aug 1987 |
JPX |
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Parent Case Info
This application is a continuation of application Ser. No. 234,171, filed on Aug. 19, 1988, now abandoned.
US Referenced Citations (4)
Foreign Referenced Citations (10)
Number |
Date |
Country |
0011184 |
May 1980 |
EPX |
0091287 |
Oct 1983 |
EPX |
60-23406 |
Feb 1985 |
JPX |
60-104111 |
Jun 1985 |
JPX |
60-104112 |
Jun 1985 |
JPX |
60-108407 |
Jun 1985 |
JPX |
60-108408 |
Jun 1985 |
JPX |
60-108410 |
Jun 1985 |
JPX |
2029426 |
Mar 1980 |
GBX |
2161169 |
Jan 1986 |
GBX |
Non-Patent Literature Citations (1)
Entry |
Chemical Abstracts, vol. 103, 1985, No. 103:105820r, "Impact Modifiers for Styrene Polymers", p. 38. |
Continuations (1)
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Number |
Date |
Country |
Parent |
234171 |
Aug 1988 |
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