GB952357A - Process for the purification of epoxy resins - Google Patents
Process for the purification of epoxy resinsInfo
- Publication number
- GB952357A GB952357A GB2972860A GB2972860A GB952357A GB 952357 A GB952357 A GB 952357A GB 2972860 A GB2972860 A GB 2972860A GB 2972860 A GB2972860 A GB 2972860A GB 952357 A GB952357 A GB 952357A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyepoxide
- acetone
- resin
- alkali salts
- purified
- 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
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/063—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with epihalohydrins
-
- 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
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)
Abstract
Glycidyl ethers of dihydric phenols, which are produced by the reaction in an alkaline medium of epichlorohydrin with a mono- or bis-nuclear compound containing two phenolic hydroxyl groups, are purified by (i) acidifying the reaction mixture, (ii) separating the crude polyepoxide from the aqueous layer, (iii) washing it with boiling water, (iv) removing the wash water, (v) completely dehydrating the washed polyepoxide in a vacuum and at a bath temperature of approximately 130 DEG C., (vi) dissolving the polyepoxide, still containing alkali salts, in acetone, (vii) removing the alkali salts, which are insoluble in acetone, from the solution by filtration, and (viii) removing the solvent from the polyepoxide by distillation. Specification 518,057 is referred to.ALSO:Epoxy resins, which are thermo setting in the presence of a hardening agent, contain more than 1 epoxy group per molecule, and are produced by the reaction in an alkaline medium of epichlorhyrdin with a mono- or bis-nuclear com, pound containing two phenolic hydroxyl groups-are purified by (i) acidifying the reaction mixture, (ii) separating the crude resin from the aqueous layer, (iii) washing it with boiling water, (iv) removing the wash water, (v) completely dehydrating the washed resin in a vacuum and at a bath temperature of approximately 130 DEG C., (vi) dissolving the resin, still containing alkali salts, in acetone, (vii) removing the alkali salts, which are insoluble in acetone, from the solution by filteration, and (viii) removing the solvent from the resin by distillation. Examples are given in which either bisphenol A or resorcinol (Example 11) is reacted with epichlorhydrin in aqueous NaOH and the resulting product is purified. Specification 518,057 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH7763159A CH382448A (en) | 1959-09-01 | 1959-09-01 | Process for cleaning hardenable epoxy resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB952357A true GB952357A (en) | 1964-03-18 |
Family
ID=4535855
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2972860A Expired GB952357A (en) | 1959-09-01 | 1960-08-29 | Process for the purification of epoxy resins |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE594104A (en) |
CH (1) | CH382448A (en) |
ES (1) | ES260674A1 (en) |
GB (1) | GB952357A (en) |
NL (1) | NL255384A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4778863A (en) * | 1987-08-13 | 1988-10-18 | The Dow Chemical Company | Preparation of epoxy resins having low undesirable halogen content |
US4785061A (en) * | 1987-08-13 | 1988-11-15 | The Dow Chemical Company | Method for reducing the aliphatic halide content of epoxy resins using a solvent mixture including a polar aprotic solvent |
-
0
- BE BE594104D patent/BE594104A/xx unknown
- NL NL255384D patent/NL255384A/xx unknown
-
1959
- 1959-09-01 CH CH7763159A patent/CH382448A/en unknown
-
1960
- 1960-08-29 GB GB2972860A patent/GB952357A/en not_active Expired
- 1960-08-30 ES ES0260674A patent/ES260674A1/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4778863A (en) * | 1987-08-13 | 1988-10-18 | The Dow Chemical Company | Preparation of epoxy resins having low undesirable halogen content |
US4785061A (en) * | 1987-08-13 | 1988-11-15 | The Dow Chemical Company | Method for reducing the aliphatic halide content of epoxy resins using a solvent mixture including a polar aprotic solvent |
Also Published As
Publication number | Publication date |
---|---|
CH382448A (en) | 1964-09-30 |
NL255384A (en) | |
BE594104A (en) | |
ES260674A1 (en) | 1960-12-16 |
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