GB757392A - Preparation of novolak resins - Google Patents
Preparation of novolak resinsInfo
- Publication number
- GB757392A GB757392A GB1648553A GB1648553A GB757392A GB 757392 A GB757392 A GB 757392A GB 1648553 A GB1648553 A GB 1648553A GB 1648553 A GB1648553 A GB 1648553A GB 757392 A GB757392 A GB 757392A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction mixture
- phenol
- reaction
- temperature
- mixture
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/12—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with monohydric phenols having only one hydrocarbon substituent ortho on para to the OH group, e.g. p-tert.-butyl phenol
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)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
A novolak resin is made by condensing a molar excess of phenolic compounds containing phenol, meta-cresol or meta-ethyl phenol with formaldehyde (formalin or paraformaldehyde) in the presence of a salt of a divalent electropositive metal with an organic acid, which salt is at least partially soluble in the reaction mixture and the pH of the reaction mixture being between 4 and 7, until there is no free formaldehyde left in the reaction mixture, raising the temperature of the mixture while allowing volatile materials to distil therefrom to a temperature above 100 DEG C. at which a further condensation takes place, allowing the further condensation reaction to proceed to completion and the water thus formed to distil from the reaction mixture, removing any unwanted unreacted phenolic compounds and cooling the reaction mixture to give a solid product. The preferred ratio of phenolic compound/formaldehyde is from 1.3:1 to 2:1. Other phenols may be mixed with the specified ones. Commercial xylenols containing m-substituted phenols can also be used. Catalysts specified are Ba, Sr, Ca, Mg, Mn, Zn, Cd, Co, Pb, Fe, Cr, Sn and Ni salts of organic acids, e.g. benzoic, formic, acetic and lactic acids, and are used in amount, e.g. of 0.1 to 5.0 per cent by weight of the phenol present. The process is effected by mixing the phenol with the aldehyde, adding the catalyst thereto and gently heating the mixture until reaction occurs. Where formalin is used the initial reaction is controlled by heating under reflux conditions, but where non-aqueous reactants are used control of heat input is necessary to prevent too great a rate of temperature increase. For the further condensation a temperature of 150 DEG to 160 DEG C. is preferred. Many examples are given showing comparative figures of moulding tests on the novel and conventional novolaks.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1648553A GB757392A (en) | 1953-06-16 | 1953-06-16 | Preparation of novolak resins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1648553A GB757392A (en) | 1953-06-16 | 1953-06-16 | Preparation of novolak resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB757392A true GB757392A (en) | 1956-09-19 |
Family
ID=10078202
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1648553A Expired GB757392A (en) | 1953-06-16 | 1953-06-16 | Preparation of novolak resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB757392A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4918994A (en) * | 1972-06-13 | 1974-02-19 | ||
JPS5964616A (en) * | 1982-10-06 | 1984-04-12 | Asahi Organic Chem Ind Co Ltd | Solid resol resin and its production |
-
1953
- 1953-06-16 GB GB1648553A patent/GB757392A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4918994A (en) * | 1972-06-13 | 1974-02-19 | ||
JPS5116079B2 (en) * | 1972-06-13 | 1976-05-21 | ||
JPS5964616A (en) * | 1982-10-06 | 1984-04-12 | Asahi Organic Chem Ind Co Ltd | Solid resol resin and its production |
JPS6223003B2 (en) * | 1982-10-06 | 1987-05-21 | Asahi Organic Chem Ind |
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