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 resins

Info

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
Application number
GB749753A
Inventor
Geoffrey Swann
Peter Gilbert Evans
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beck Koller and Company England Ltd
Original Assignee
Beck Koller and Company England Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Beck Koller and Company England Ltd filed Critical Beck Koller and Company England Ltd
Priority to GB749753A priority Critical patent/GB724972A/en
Publication of GB724972A publication Critical patent/GB724972A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/40Chemically modified polycondensates
    • C08G12/42Chemically modified polycondensates by etherifying
    • C08G12/424Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds
    • C08G12/425Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds based on triazines
    • C08G12/427Melamine

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.
GB749753A 1953-03-18 1953-03-18 Improvements in or relating to the manufacture of etherified melamine-formaldehyde resins Expired GB724972A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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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