GB776495A - Process for the production of hardenable condensation products - Google Patents
Process for the production of hardenable condensation productsInfo
- Publication number
- GB776495A GB776495A GB16221/55A GB1622155A GB776495A GB 776495 A GB776495 A GB 776495A GB 16221/55 A GB16221/55 A GB 16221/55A GB 1622155 A GB1622155 A GB 1622155A GB 776495 A GB776495 A GB 776495A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenol
- novolak
- cresol
- epichlorhydrin
- formaldehyde
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/28—Chemically modified polycondensates
-
- 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
- C08G59/08—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols from phenol-aldehyde condensates
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Epoxy Resins (AREA)
Abstract
Epoxy resins soluble in the usual solvents for such resins, e.g. ketones and glycol monoethers, and suitable for casting or for electrical insulation, are produced by reacting an epihalogenhydrin in alkaline medium with a novolak which has been produced by reacting excess phenol with formaldehyde under acid conditions, separating the aqueous layer and distilling to remove excess phenol and render the resin anhydrous, excess phenol being added during the novolak-epichlorhydrin reaction; alternatively the novolak containing the original excess phenol and without dehydration may be reacted with the epichlorhydrin. The additional phenol added may be phenol, cresol, xylenol, chlorphenol or their glycide ethers may be employed. The optimum formaldehyde/phenol ratio for the production of the novolak is 0.5, but for phenol homologues, e.g. p- or o-cresol the ratio may be somewhat higher. The product may be mixed with fillers or dyestuffs and then hardened by addition of conventional hardening agents, e.g. amines-triethanolamine or piperidine, or polybasic acids or their anhydrides, e.g. phthalic and maleic acids, (1) 440 gs. novolak produced by reacting formaldehyde and phenol in molar ratio 0.5/1 and freeing the product of water and phenol by distillation is mixed with 170 gs. phenol dissolved in 2400 gs. 10 per cent NaOH solution and 556 gs. epichlorhydrin are added, the resulting exothermic reaction being maintained at 80 DEG C. by cooling; the resin is dehydrated by decantation, distillation and purified by solution in acetone and filtering followed by distillation or reduced pressure. In Examples (2)-(5), the novolak obtained in Example (1) is reacted with epichlorhydrin and (2) cresol, (3) xylenol, (4) glycide phenol ether, (7) chlorphenol. In Examples (5) and (6) a cresol-formaldehyde novolak is reacted, (5) with phenol, and (6) with cresol. Example (8), 1410 gs. phenol, 645 gs. 36 per cent formaldehyde and 14 gs. oxalic acid are boiled under reflux; the CH2O content of the aqueous layer is then 0.2-0.3 per cent 600 gs. NaOH dissolved in 6000 gs. water are added, the mixture is heated to 60 DEG C. and 1390 gs. epichlorhydrin added; after decantation, washing and filtration, 1840 gs. resin are obtained.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE334654X | 1954-06-04 | ||
DE160654X | 1954-06-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB776495A true GB776495A (en) | 1957-06-05 |
Family
ID=25753573
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16221/55A Expired GB776495A (en) | 1954-06-04 | 1955-06-06 | Process for the production of hardenable condensation products |
Country Status (4)
Country | Link |
---|---|
CH (1) | CH334654A (en) |
FR (1) | FR1125761A (en) |
GB (1) | GB776495A (en) |
NL (2) | NL197796A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1132729B (en) * | 1958-10-31 | 1962-07-05 | Elizabeth Shen Lo | Process for the production of epoxy resins |
DE1148077B (en) * | 1958-04-01 | 1963-05-02 | Ciba Geigy | Process for the preparation of fusible glycidyl polyethers |
GB2128616A (en) * | 1982-08-20 | 1984-05-02 | Sumitomo Chemical Co | Glycidyl ether of novolak type substituted phenolic resin and its production |
-
0
- NL NL100644D patent/NL100644C/xx active
- NL NL197796D patent/NL197796A/xx unknown
-
1955
- 1955-06-03 CH CH334654D patent/CH334654A/en unknown
- 1955-06-03 FR FR1125761D patent/FR1125761A/en not_active Expired
- 1955-06-06 GB GB16221/55A patent/GB776495A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1148077B (en) * | 1958-04-01 | 1963-05-02 | Ciba Geigy | Process for the preparation of fusible glycidyl polyethers |
DE1132729B (en) * | 1958-10-31 | 1962-07-05 | Elizabeth Shen Lo | Process for the production of epoxy resins |
GB2128616A (en) * | 1982-08-20 | 1984-05-02 | Sumitomo Chemical Co | Glycidyl ether of novolak type substituted phenolic resin and its production |
Also Published As
Publication number | Publication date |
---|---|
FR1125761A (en) | 1956-11-07 |
NL197796A (en) | |
CH334654A (en) | 1958-12-15 |
NL100644C (en) |
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