GB724972A - Improvements in or relating to the manufacture of etherified melamine-formaldehyde resins - Google Patents
Improvements in or relating to the manufacture of etherified melamine-formaldehyde resinsInfo
- Publication number
- GB724972A GB724972A GB749753A GB749753A GB724972A GB 724972 A GB724972 A GB 724972A GB 749753 A GB749753 A GB 749753A GB 749753 A GB749753 A GB 749753A GB 724972 A GB724972 A GB 724972A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formaldehyde
- butanol
- melamine
- hydroxide
- xylene
- 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/40—Chemically modified polycondensates
- C08G12/42—Chemically modified polycondensates by etherifying
- C08G12/424—Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds
- C08G12/425—Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds based on triazines
- C08G12/427—Melamine
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
An etherified melamine-formaldehyde resin is made by condensing melamine with aqueous formaldehyde, or a substance yielding formaldehyde, in presence of an alkaline catalyst which is calcium, barium or strontium hydroxide and condensing the product, preferably after removal of most of the water, with an aliphatic monohydric alcohol containing 3-5 carbon atoms in the presence of an acidic catalyst which is provided by passing a stream of carbon dioxide through the reaction mixture. The alkaline catalyst of the first stage is precipitated as carbonate in the second stage and may be filtered off. Preferably 3.5-7 moles of formaldehyde and 4.5-7 moles of alcohol are employed per mole of melamine. In examples: (1) melamine and formaldehyde are heated to 80 DEG C. in a solution adjusted to pH 7.7-8.0 with barium p hydroxide. When a sample retains its clarity when cooled to 25 DEG C. and is completely miscible with cold water, the pH is adjusted to 7.7 with further barium hydroxide and most of the water distilled off. Butanol is then added and the mixture heated whilst passing carbon dioxide through it, the butanol distilling off being returned to the reaction vessel. Heating is continued till the product is completely miscible with xylene; (2) and (3) as in (1) but using strontium or calcium hydroxide instead of barium hydroxide; (6) as in (1) but using isobutanol instead of n-butanol; (7) as in (1) but using amyl alcohol instead of butanol and stopping the etherification when the miscibility with xylene reaches a maximum value; (4) and (5) melamine and formaldehyde are heated to 80 DEG C. in a solution adjusted to pH 7.7-8.0 with barium hydroxide until a sample of the product shows an acetone tolerance of 3.5-4. After adjusting the pH to 7.7 with further barium hydroxide, most of the water is removed, n-butanol is added and the mixture heated whilst passing carbon dioide through it and returning butanol to the reaction vessel. Heating is continued until the miscibility of the resin with xylene reaches a maximum value; (8) melamine is condensed with formaldehyde as in example (1). n-Propanol and xylene are added to the condensate and the mixture heated whilst passing a stream of carbon dioxide through it. The distillate separates into two layers and the upper propanol-rich layer is returned to the reaction vessel. Heating is continued until the miscibility of the resin with xylene reaches a maximum value.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB749753A GB724972A (en) | 1953-03-18 | 1953-03-18 | Improvements in or relating to the manufacture of etherified melamine-formaldehyde resins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB749753A GB724972A (en) | 1953-03-18 | 1953-03-18 | Improvements in or relating to the manufacture of etherified melamine-formaldehyde resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB724972A true GB724972A (en) | 1955-02-23 |
Family
ID=9834258
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB749753A Expired GB724972A (en) | 1953-03-18 | 1953-03-18 | Improvements in or relating to the manufacture of etherified melamine-formaldehyde resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB724972A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3392150A (en) * | 1959-07-23 | 1968-07-09 | Herbert P.A. Groll | Etherified amino formaldehyde products |
WO2017102076A1 (en) | 2015-12-16 | 2017-06-22 | Ineos Melamines Gmbh | Process for manufacturing solutions of alkylated amino formaldehyde resins having a low free formaldehyde content |
-
1953
- 1953-03-18 GB GB749753A patent/GB724972A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3392150A (en) * | 1959-07-23 | 1968-07-09 | Herbert P.A. Groll | Etherified amino formaldehyde products |
WO2017102076A1 (en) | 2015-12-16 | 2017-06-22 | Ineos Melamines Gmbh | Process for manufacturing solutions of alkylated amino formaldehyde resins having a low free formaldehyde content |
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