GB878750A - Epoxide compositions - Google Patents
Epoxide compositionsInfo
- Publication number
- GB878750A GB878750A GB461459A GB461459A GB878750A GB 878750 A GB878750 A GB 878750A GB 461459 A GB461459 A GB 461459A GB 461459 A GB461459 A GB 461459A GB 878750 A GB878750 A GB 878750A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenol
- resorcinol
- epoxy
- group
- methyl
- 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
- C08G59/40—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 curing agents used
- C08G59/50—Amines
- C08G59/56—Amines together with other curing agents
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A hardenable composition comprises an epoxide compound having an epoxy-equivalency greater than 1,0, a hardener therefore which is a polyamine or mixture of polyamines and an accelerator for the hardening reaction which is the product of reacting a phenol containing at least one reactive hydrogen atom in the ortho or para position with respect to the phenolic hydroxyl group or groups in the presence of an acid catalyst with a vinyl of the general formula: CH2=CRX wherein R represents a hydrogen atom or a methyl group and X represents a phenyl group, a phenyl group substituted by an alkyl or vinyl group, a chlorine atom, an alkoxy-carbonyl group, an acyloxy group or a 2-pyrrolidone group. Specified epoxy compounds are butadiene dioxide, 1 : 2 : 5 : 6-diepoxyhexane, 1 : 2 : 4 : 5-diepoxy-cyclohexane, methyl-9 : 10 : 12 : 13-diepoxy stearate, the dimethyl ester of 6 : 7 : 10 : 11-diepoxy-hexadecane-1 : 16-di-boxylic acid, diethylene glycol bis-(3 : 4-epoxy-cyclohexane carboxylate), 3 : 4-epoxy-cyclo-hexylmethyl-3 : 4-epoxy-cyclohexane carboxylate, epichlorohydrin reaction products of aniline or 4 : 41-di (monomethylamino)-diphenyl methane, polyglycidyl esters and polyglycidyl ethers of which many are specified. Two methods are disclosed for preparing the condensate of the phenol and the vinyl compound, with and without solvent, catalysts specified for this reaction being hydrochloric, sulphuric and toluene-p-sulphonic acid, aluminium chloride, zinc chloride, stannic chloride, antimony chloride and boron trifluoride and its complexes. The Specification discloses reaction products made from phenol and styrene, phenol and divinyl benzene, bis-phenol A and styrene, bis-phenol A and divinyl benzene, resorcinol and styrene, resorcinol and methyl styrene, resorcinol and divinylbenzene, resorcinol and methyl isopropenyl ketone, resorcinol and vinyl pyrrolidone, resorcinol and methyl acrylate and resorcinol and vinyl acetate. The examples describe the admixture and sub-sequential curing of an epoxy resin derived from bis-phenol A and epichlorohydrin with p, p1-diaminodiphenyl methane, diethylaminopropylamine, m-phenylene diamine and 2 : 4 : 6-tris (dimethylaminomethyl) phenol and selected accelerators.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB461459A GB878750A (en) | 1959-02-10 | 1959-02-10 | Epoxide compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB461459A GB878750A (en) | 1959-02-10 | 1959-02-10 | Epoxide compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB878750A true GB878750A (en) | 1961-10-04 |
Family
ID=9780492
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB461459A Expired GB878750A (en) | 1959-02-10 | 1959-02-10 | Epoxide compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB878750A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3203920A (en) * | 1961-11-20 | 1965-08-31 | Ciba Ltd | Curable mixtures containing epoxy resins, curing agents and flexibilizers |
-
1959
- 1959-02-10 GB GB461459A patent/GB878750A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3203920A (en) * | 1961-11-20 | 1965-08-31 | Ciba Ltd | Curable mixtures containing epoxy resins, curing agents and flexibilizers |
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