US4251650A
Expired / Lapsed
US
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Process for the polymerization of ethylene in the presence of silyl ethers as initiators
Assignee: Bayer AG
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Filing: 1979-09-14
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Granted: 1981-02-17
•
Expires: 1999-09-14
Abstract
Abstract A process for the copolymerization of ethylene at pressures of from 200 to 3500 atms and temperatures of from 130° to 300° C., wherein silyl ethers are used as initiators.
Inventors
- 👤 Fritz Mietzsch
- 👤 Hans Rudolph
- 👤 Heinrich Wolfers
- 👤 Heinrich Alberts
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-27 22:24
CPC Classifications
C; C08; C08F; C08F10/00; C08F10/02
Claims Analysis
Total Claims: 5
Claim 1
Independent Claim
217 words
A process for the production of homopolymers or copolymers of ethylene by radical polymerisation at a temperature of at least 100° C. and under a pressure of from 200 to 3500 atms, optionally in the presence of a solvent, wherein as the initiators a silyl ether corresponding to the general formula I is used: ##STR7## R 1 represents methyl, ethyl, phenyl, benzyl or chloromethyl; R 2 represents chlorine, hydroxyl, methoxy, ethoxy or R 1 ; R 4 and R 5 the same or different represent aryl radicals optionally substituted by C 1 -C 4 -alkyl, methoxy, chlorine, or fluorine; R 6 and R 7 the same or different either have the same meaning as R 4 and R 5 or represent C 1 -C 6 -alkyl radicals optionally substituted by C 1 -C 4 -alkyl, methoxy, chlorine or fluorine, cycloalkyl radicals containing from 5 to 7 carbon atoms or hydrogen; R 8 represents hydrogen or a silyl radical corresponding to the general formula II: ##STR8## wherein R 2 has the meaning given above; and n is an integer of from 1 to 20, m is an integer from 1 to 10, is 0 or 1; R 9 represents R 1 or X R 10 represents R 2 or X and R 11 represents chlorine, hydroxyl or X.
Claim 2
Dependent Claim
217 words
A process for the production of homopolymers or copolymers of ethylene by radical polymerisation at a temperature of at least 100° C. and under a pressure of from 200 to 3500 atms, optionally in the presence of a solvent, wherein as the initiators a silyl ether corresponding to the general formula I is used: ##STR7## R 1 represents methyl, ethyl, phenyl, benzyl or chloromethyl; R 2 represents chlorine, hydroxyl, methoxy, ethoxy or R 1 ; R 4 and R 5 the same or different represent aryl radicals optionally substituted by C 1 -C 4 -alkyl, methoxy, chlorine, or fluorine; R 6 and R 7 the same or different either have the same meaning as R 4 and R 5 or represent C 1 -C 6 -alkyl radicals optionally substituted by C 1 -C 4 -alkyl, methoxy, chlorine or fluorine, cycloalkyl radicals containing from 5 to 7 carbon atoms or hydrogen; R 8 represents hydrogen or a silyl radical corresponding to the general formula II: ##STR8## wherein R 2 has the meaning given above; and n is an integer of from 1 to 20, m is an integer from 1 to 10, is 0 or 1; R 9 represents R 1 or X R 10 represents R 2 or X and R 11 represents chlorine, hydroxyl or X.
Claim 3
Dependent Claim
22 words
A process as claimed in claim 1, wherein the silyl ether has a molecular weight M n of from 2000 to 8000.
Claim 4
Dependent Claim
48 words
A process as claimed in claim 1, wherein R 4 and R 5 represent phenyl, tolyl, p-tert.-butyl phenyl, o and p-chlorophenyl, 2,4-dichlorophenyl, naphthyl, biphenylyl, or m-methoxy phenyl; and R 6 and R 7 represent R 4 or R 5 as claimed herein or methyl, ethyl, isopropyl or cyclohexyl.
Claim 5
Dependent Claim
169 words
A process as claimed in claim 1, wherein the silyl ether is the reaction product of the following compounds (B) and (C) in the presence of a metal (A): ______________________________________
(A) (B) (C)
______________________________________
1) magnesium benzaldehyde trichloromethyl silane
2) magnesium benzaldehyde trichlorophenyl silane
3) magnesium benzaldehyde dichlorodimethyl silane
4) magnesium acetophenone trichloromethyl silane
5) sodium acetophenone diphenyl dichlorosilane
6) magnesium propiophenone
trichloromethyl silane
7) lithium isopropyl phenyl
trichloromethyl silane
ketone
8) magnesium cyclohexyl phenyl
trichloromethyl silane
ketone
9) magnesium benzophenone trichloromethyl silane
10) magnesium benzophenone dichlorodimethyl silane
11) sodium benzophenone trichlorophenyl silane
12) lithium 4,4-dimethyl trichloromethyl silane
benzophenone
13) potassium benzophenone dichlorodiphenyl silane
14) calcium 4-t-butyl benzo
trichloromethyl silane
phenone
15) magnesium 4-chlorobenzo-
trichloromethyl silane
phenone
16) sodium 2-methyl benzo-
dichlorodimethyl silane
phenone
17) magnesium 2-chlorobenzo-
trichloromethyl silane
phenone
18) magnesium 2,4-dichlorobenzo-
trichloroethyl silane
phenone
19) magnesium 3-methoxy benzo-
dichloroethoxy methyl
phenone silane
20) magnesium naphthylphenyl
trichloromethyl silane
ketone
21) magnesium 4-phenyl benzo-
trichloromethyl silane
phenone
22) magnesium 4-benzoyl benzo-
trichloromethyl silane
phenone
23) magnesium benzaldehyde tetrachlorosilane
______________________________________
References Cited (Backward Citations)
US3792126A
Cited
US3931355A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1984-02-17 | 1984-08-18 | 1985-02-17 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1988-02-17 | 1988-08-18 | 1989-02-17 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1992-02-17 | 1992-08-18 | 1993-02-17 | $7700.00 | Window Closed / Lapsed |