GB1212351A - Polymerisation process for preparing lactone polymer compositions - Google Patents
Polymerisation process for preparing lactone polymer compositionsInfo
- Publication number
- GB1212351A GB1212351A GB2287167A GB2287167A GB1212351A GB 1212351 A GB1212351 A GB 1212351A GB 2287167 A GB2287167 A GB 2287167A GB 2287167 A GB2287167 A GB 2287167A GB 1212351 A GB1212351 A GB 1212351A
- Authority
- GB
- United Kingdom
- Prior art keywords
- glycol
- specified
- resin
- ketone
- alkyl derivatives
- 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
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/60—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
- C08G63/08—Lactones or lactides
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)
Abstract
1,212,351. Polymerizing lactones in the presence of preformed polymers. LAPORTCHEMICALS Ltd. 14 Aug., 1968 [17 May, 1967], No. 22871/67. Headings C3P and C3R. A lactone of formula where n is 3-6, R is H, Me, Et, n-Pr, iso-Pr, Cl or Br, and wherein the total number of carbon atoms in all the R groups does not exceed 12 and the total number of halogen atoms in all the R groups does not exceed 2 is polymerized in the presence of a preformed polymer which has at least one alcoholic-OH group and is (a) an unsaturated polyester having two or more ethylenic double bonds per molecule, (b) a ketone formaldehyde resin or (c) a ketone methanol resin. Specified lactones are epsilon caprolactone and methyl epsilon caprolactone or mixtures thereof. Specified for (a) are polyesters of ethylene glycol, diethylene glycol, propylene glycol and dipropylene glycol with maleic acid or anhydride. Specified ketones for (b) are cyclohexanone or alkyl derivatives thereof, cyclopentanone or alkyl derivatives thereof, methyl ethyl ketone or diethyl ketone. Specified ketones for (c) are cyclohexanone, cyclopentanone or alkyl derivatives thereof. Catalysts, e.g. HC1, H 2 SO 4 , H 3 PO 4 , CH 3 CO 2 H, CCl 3 CO 2 H, CF 3 CO 2 H, ZnCl 2 , Zn 3 (BO 4 ) 2 , dibutyl tin oxide or hexylene glycol titanate may be used. The examples disclose polymerization of epsilon caprolactone with (1) maleic anhydrideethylene glycol polyester, (2) cyclohexanoneformaldehyde resin and (3) cyclohexanonemethanol resin. The final unsaturated polymers may be cured with a vinyl monomer, e.g. styrene, methyl methacrylate or diallyl phthalate. . Reference has been directed by the Comptroller to Specification 859,642.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2287167A GB1212351A (en) | 1967-05-17 | 1967-05-17 | Polymerisation process for preparing lactone polymer compositions |
NL6807023A NL6807023A (en) | 1967-05-17 | 1968-05-17 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2287167A GB1212351A (en) | 1967-05-17 | 1967-05-17 | Polymerisation process for preparing lactone polymer compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1212351A true GB1212351A (en) | 1970-11-18 |
Family
ID=10186368
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2287167A Expired GB1212351A (en) | 1967-05-17 | 1967-05-17 | Polymerisation process for preparing lactone polymer compositions |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB1212351A (en) |
NL (1) | NL6807023A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2162527A (en) * | 1984-07-28 | 1986-02-05 | Daicel Chem | Process for producing lactone polymer and thermosetting resin composition containing said lactone polymer as an anti-shrinking agent |
-
1967
- 1967-05-17 GB GB2287167A patent/GB1212351A/en not_active Expired
-
1968
- 1968-05-17 NL NL6807023A patent/NL6807023A/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2162527A (en) * | 1984-07-28 | 1986-02-05 | Daicel Chem | Process for producing lactone polymer and thermosetting resin composition containing said lactone polymer as an anti-shrinking agent |
Also Published As
Publication number | Publication date |
---|---|
NL6807023A (en) | 1968-11-18 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |