GB724032A - Improvements in or relating to the production of polymers - Google Patents
Improvements in or relating to the production of polymersInfo
- Publication number
- GB724032A GB724032A GB22388/52A GB2238852A GB724032A GB 724032 A GB724032 A GB 724032A GB 22388/52 A GB22388/52 A GB 22388/52A GB 2238852 A GB2238852 A GB 2238852A GB 724032 A GB724032 A GB 724032A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diol
- propene
- methylene
- acetal
- bis
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F24/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
The bulk polymerization of dioxolanes having one or more semi-cyclic double linkages is catalized with an addition compound of a polar solvent and a hydrohalide acid salt of a metal of the second or fourth group of the periodic table. Suitable catalysts are methyl or ethyl alcohol solutions of zinc, mercuric, cadmium and stannous chlorides. Examples describe the polymerization of (1) propene (1)-diol-(2,3)-cyclohexylidene acetal; (2) propene-(1)-diol-(2,3)-cyclopentylidene acetal; (3) and (4) cyclohexane dione-(1,4)-bis-[propene-(1)-diol(2,3)-acetal] dissolved in the acetal of (1); (5) 1,4-bis-[2,21-(4-methylene-1,3-dioxolyl]-butane or the di-[propene-(1)-diol-(2,3)-acetal] of adipic dialdehyde; (6) and (9) bis-2,21-(4-methylene-dioxolane); (7) a mixture of cyclohexanone-propane-(1)-diol-(2,3)-ketal and (6); (8) a mixture of cyclohexane-dione-1,4-bis-[propene-(1)-diol-(2,3)-ketal] and (6). Other dioxolanes mentioned are 4-methylene-, 2-propyl-4-methylene-, 2 - vinyl - 4 - methylene -, 2 - phenyl - 4 - methylene- and 4 - methylene - 5 - methyl - 1,3-di - oxolanes, propene-(1) - diol - (2,3) - methylcyclohexylidene acetal, 2 - methyl - 4 - methylene - 1,3 - dioxolane - 2 - acetic acid ethyl ester, 1,2 - and 1,3 - bis - [propene - (1) - diol - (2,3) - acetal], the di - [propene - (1) - diol - (2,3) - acetal] of malonaldehyde, succinaldehyde and glutaraldehyde. The polymerization may be carried out by dropwise addition of the catalyst at room temperature, the temperature rising to 38 DEG to 40 DEG C., which is maintained for 8 to 12 hours, followed by heating at 60 DEG C. for 1 to 2 hours. The products are compatible with nitro-ceullose and may be used for moulding and in lacquers. Specification 620,842 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE724032X | 1951-09-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB724032A true GB724032A (en) | 1955-02-16 |
Family
ID=6633686
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB22388/52A Expired GB724032A (en) | 1951-09-08 | 1952-09-05 | Improvements in or relating to the production of polymers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB724032A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5304611A (en) * | 1992-12-30 | 1994-04-19 | Eastman Kodak Company | Copolymers of vinyl dioxolanes and imidized derivatives of maleic anhydride |
EP1090916A1 (en) * | 1999-10-06 | 2001-04-11 | Dainippon Ink And Chemicals, Inc. | 4-methylene-1,3-dioxolanes having functional groups |
EP1182201A1 (en) * | 2000-08-25 | 2002-02-27 | Dainippon Ink And Chemicals, Inc. | 4-Methylene-1,3-dioxolanes as cross-linking agents |
-
1952
- 1952-09-05 GB GB22388/52A patent/GB724032A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5304611A (en) * | 1992-12-30 | 1994-04-19 | Eastman Kodak Company | Copolymers of vinyl dioxolanes and imidized derivatives of maleic anhydride |
US5418294A (en) * | 1992-12-30 | 1995-05-23 | Eastman Chemical Company | Copolymers of vinyl dioxolanes and imidized derivatives of maleic anhydride |
US5446106A (en) * | 1992-12-30 | 1995-08-29 | Eastman Chemical Company | Copolymers of vinyl dioxolanes and imidized derivatives of maleic anhydride |
EP1090916A1 (en) * | 1999-10-06 | 2001-04-11 | Dainippon Ink And Chemicals, Inc. | 4-methylene-1,3-dioxolanes having functional groups |
JP2001158781A (en) * | 1999-10-06 | 2001-06-12 | Dainippon Ink & Chem Inc | 4-methylene-1,3-dioxolane containing functional group and method for producing the same |
EP1182201A1 (en) * | 2000-08-25 | 2002-02-27 | Dainippon Ink And Chemicals, Inc. | 4-Methylene-1,3-dioxolanes as cross-linking agents |
JP2002155073A (en) * | 2000-08-25 | 2002-05-28 | Dainippon Ink & Chem Inc | 4-methylene-1,3-dioxolane compound, method for producing the same, photocationic cross-linking composition and transparent film |
US6844375B2 (en) | 2000-08-25 | 2005-01-18 | Dainippon Ink And Chemicals, Inc. | 4-methylene-1,3-dioxolanes as cross-linking agents |
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