GB848678A - Resinous compositions - Google Patents
Resinous compositionsInfo
- Publication number
- GB848678A GB848678A GB7646/57A GB764657A GB848678A GB 848678 A GB848678 A GB 848678A GB 7646/57 A GB7646/57 A GB 7646/57A GB 764657 A GB764657 A GB 764657A GB 848678 A GB848678 A GB 848678A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formaldehyde
- epoxy resin
- acid
- melamine
- fluid
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Epoxy Resins (AREA)
- Paints Or Removers (AREA)
Abstract
The invention comprises a process for preparing a fluid resinous composition stable in storage by heating together, in the presence of an acid catalyst which is at least as strong as phosphoric acid and which maintains an acid system in solution in a mutual solvent, an organic solvent-soluble etherified urea-formaldehyde or etherified melamine formaldehyde resinous condensation product and an epoxy resin produced from epichlorhydrin and a dihydric phenol, in proportions based on total solids weight of from 30% to 80% of the aminoplast resin and from 70% to 20% of the epoxy resin, at a temperature between 70 DEG C. and the boiling point of the solution under conditions such that there is retained sufficient of the solvent to ensure that the composition is fluid and remains fluid after it has been cooled. Suitable aminoplastic resins are urea-formaldehyde or melamine-formaldehyde resins etherified with, for example, methanol, ethanol, propanol, butanol, isobutanol or higher alcohols, in solution in the etherifying alcohol or partly or wholly replaced by, e.g. xylene or ethyl glycol acetate. Phosphoric acid and p-toluene sulphonic acid (which may be partly neutralised, e.g. with morpholine) and hydrochloric acid are suitable acid catalysts. In an example (1) an epoxy resin from epichlorhydrin and diphenylol propane, a butanol solution of butylated melamine formaldehyde resin and xylol are heated in the presence of phosphoric acid up to 100 DEG C. The fluid product obtained was cured as a film by heating at 180 DEG C. Other examples are given in some of which the epoxy resin has been previously reacted with refined soya bean oil and the aminoplast is selected from butylated melamine-formaldehyde and urea-formaldehyde resins and tri- or hexa(methoxymethyl) melamine. The Provisional Specification includes also an example employing 610 parts of epoxy resin and 107 parts of butylated melamine formaldehyde resin, the solution produced being used to bond a sheet of copper foil to a phenolic laminate.ALSO:A fluid resinous composition, suitable as a stoving lacquer, is prepared by heating together, in the presence of an acid catalyst which is at least as strong as phosphoric acid and which maintains an acid system, in solution in a mutual solvent, an organic solventsoluble etherified urea - formaldehyde or etherified melamine - formaldehyde resinous condensation product and an epoxy resin produced from epichlorhydrin and a dihydric phenol, in proportions based on total solids weight of from 30% to 80% of the aminoplast resin and from 70% to 20% of the epoxy resin at a temperature between 70 DEG C. and the boiling point of the solution under conditions such that there is retained sufficient of the solvent to ensure that the composition is fluid and remains fluid after it has been cooled. Phosphoric acid and p-toluene sulphonic acid (which may be partly neutralized e.g. with morpholine) and hydrochloric acid are suitable catalysts. In an Example (1) an epoxy resin from epichlorhydrin and diphenylolpropane, a butanol solution of butylated melamineformaldehyde resin are heated with xylol and phosphoric acid up to 100 DEG C. The fluid product is flowed on to a tin plate and cured at 180 DEG C. to give a hard film. Other examples are given in which the epoxy resin has previously been reacted with refined soya bean oil and the aminoplast is a butylated melamine-formaldehyde or urea-formaldehyde resin or a tri- or hexa - methoxymethyl melamine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH5673658A CH371202A (en) | 1957-03-07 | 1958-03-07 | Process for manufacturing a resinous composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH843861A CH371092A (en) | 1961-07-18 | 1961-07-18 | Filter apparatus for use in a liquid circulation system |
Publications (1)
Publication Number | Publication Date |
---|---|
GB848678A true GB848678A (en) | 1960-09-21 |
Family
ID=4340343
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7646/57A Expired GB848678A (en) | 1957-03-07 | 1957-03-07 | Resinous compositions |
Country Status (5)
Country | Link |
---|---|
CH (1) | CH371092A (en) |
DE (1) | DE1156558B (en) |
FR (1) | FR1192704A (en) |
GB (1) | GB848678A (en) |
NL (1) | NL102187C (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1162076B (en) * | 1961-10-25 | 1964-01-30 | Teerverwertung Gmbh | Hardening of compounds with more than one epoxy group per molecule |
DE1199994B (en) * | 1962-01-27 | 1965-09-02 | Leuna Werke Veb | Process for the production of cured products based on polyepoxides at room temperature |
DE1298715B (en) * | 1961-02-15 | 1969-07-03 | Bakelite Ltd | Process for the production of coverings and coverings based on epoxy polyadducts |
CN114249998A (en) * | 2020-09-25 | 2022-03-29 | 广东华润涂料有限公司 | Michael addition-curable compositions, coating compositions comprising the same, and coated articles made therefrom |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL288563A (en) * | 1962-02-23 | 1900-01-01 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2528359A (en) * | 1946-04-10 | 1950-10-31 | Devoe & Raynolds Co | Polyepoxide-containing compositions and reaction products |
US2541027A (en) * | 1948-05-11 | 1951-02-13 | Shell Dev | Compositions of matter containing epoxy ethers and phosphorus-containing compounds |
NL182879B (en) * | 1951-02-26 | Dow Chemical Co | PROCEDURE FOR THE PREPARATION OF A HERBICIDE PREPARATION, AND SUITABLE SUBSTITUTED 2-PHENYL-2-ETHYLOXIRAN COMPOUNDS FOR THIS. | |
BE519171A (en) * | 1952-04-14 |
-
1957
- 1957-03-07 GB GB7646/57A patent/GB848678A/en not_active Expired
-
1958
- 1958-03-05 FR FR1192704D patent/FR1192704A/en not_active Expired
- 1958-03-06 DE DEB48087A patent/DE1156558B/en active Pending
- 1958-03-06 NL NL225561A patent/NL102187C/xx active
-
1961
- 1961-07-18 CH CH843861A patent/CH371092A/en unknown
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1298715B (en) * | 1961-02-15 | 1969-07-03 | Bakelite Ltd | Process for the production of coverings and coverings based on epoxy polyadducts |
DE1162076B (en) * | 1961-10-25 | 1964-01-30 | Teerverwertung Gmbh | Hardening of compounds with more than one epoxy group per molecule |
DE1199994B (en) * | 1962-01-27 | 1965-09-02 | Leuna Werke Veb | Process for the production of cured products based on polyepoxides at room temperature |
CN114249998A (en) * | 2020-09-25 | 2022-03-29 | 广东华润涂料有限公司 | Michael addition-curable compositions, coating compositions comprising the same, and coated articles made therefrom |
Also Published As
Publication number | Publication date |
---|---|
CH371092A (en) | 1963-08-15 |
NL102187C (en) | 1962-08-15 |
DE1156558B (en) | 1963-10-31 |
FR1192704A (en) | 1959-10-28 |
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