GB792702A - Curing of liquid polyepoxide resins - Google Patents
Curing of liquid polyepoxide resinsInfo
- Publication number
- GB792702A GB792702A GB1256354A GB1256354A GB792702A GB 792702 A GB792702 A GB 792702A GB 1256354 A GB1256354 A GB 1256354A GB 1256354 A GB1256354 A GB 1256354A GB 792702 A GB792702 A GB 792702A
- Authority
- GB
- United Kingdom
- Prior art keywords
- catalyst
- per cent
- epichlorhydrin
- butanol
- hardened
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
- C08G59/72—Complexes of boron halides
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
- C08G59/145—Compounds containing one epoxy group
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Reinforced Plastic Materials (AREA)
- Laminated Bodies (AREA)
Abstract
Liquid polyepoxide resins prepared from dihydric phenols and more epichlorhydrin and having at least two epoxide groups per molecule and more epoxide groups than hydroxyl groups and free from functional groups other than hydroxyl are cured by addition of FriedelCrafts catalysts preferably in the presence of diluents neutral to the catalyst and polyepoxide, e.g. dibutyl phthalate, chlorinated polyphenols. There also may be present as diluents compounds which are polymerized by the catalyst, e.g. phenyl glycidylether, allyl glycidylether, epichlorhydrin, turpentine, styrene oxide. Suitable catalysts are boron trifluoride complexes with ether, water, acetic acid and butanol; stannic chloride, antimony pentachloride. The catalyst and resin may be applied from jets of a spray gun on to the surfaces to be united, e.g. glass cloth or laminates. In examples: (1) "Technical TPG" was hardened by addition of antimony pentachloride in butyl acetate; (3) the resin as in (1) mixed with a 10 per cent solution of boron fluoride etherate in methyl ethyl ketone and aluminium powder was poured into a mould and hardened in 3 minutes without shrinking; (5) "Technical DPG" containing 25 per cent epichlorhydrin was sprayed from one jet of a twin jet gun and a 10 per cent solution of boron fluoride/butanol in butanol was sprayed from the secondary jet to give a 4 per cent concentration of catalyst. The sprayed panels were coated with thick films of high gloss which hardened in 8 minutes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1256354A GB792702A (en) | 1954-04-30 | 1954-04-30 | Curing of liquid polyepoxide resins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1256354A GB792702A (en) | 1954-04-30 | 1954-04-30 | Curing of liquid polyepoxide resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB792702A true GB792702A (en) | 1958-04-02 |
Family
ID=10006966
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1256354A Expired GB792702A (en) | 1954-04-30 | 1954-04-30 | Curing of liquid polyepoxide resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB792702A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3080341A (en) * | 1959-12-16 | 1963-03-05 | Martin Marietta Corp | Processes for curing epoxy resins |
US3109827A (en) * | 1958-05-08 | 1963-11-05 | Boake Roberts & Company Ltd A | New reaction products of epoxidized oils and an antimony halide |
US3287318A (en) * | 1961-08-10 | 1966-11-22 | Pittsburgh Plate Glass Co | Substantially neutral electrophilic salts as curing catalyst for amidealdehyde resins |
-
1954
- 1954-04-30 GB GB1256354A patent/GB792702A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3109827A (en) * | 1958-05-08 | 1963-11-05 | Boake Roberts & Company Ltd A | New reaction products of epoxidized oils and an antimony halide |
US3080341A (en) * | 1959-12-16 | 1963-03-05 | Martin Marietta Corp | Processes for curing epoxy resins |
US3287318A (en) * | 1961-08-10 | 1966-11-22 | Pittsburgh Plate Glass Co | Substantially neutral electrophilic salts as curing catalyst for amidealdehyde resins |
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