GB683918A - Improvements in or relating to the production of melamine-formaldehyde condensation products - Google Patents

Improvements in or relating to the production of melamine-formaldehyde condensation products

Info

Publication number
GB683918A
GB683918A GB1435450A GB1435450A GB683918A GB 683918 A GB683918 A GB 683918A GB 1435450 A GB1435450 A GB 1435450A GB 1435450 A GB1435450 A GB 1435450A GB 683918 A GB683918 A GB 683918A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
melamine
mols
succinimide
mol
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
GB1435450A
Inventor
Geoffrey Swann
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 GB1435450A priority Critical patent/GB683918A/en
Publication of GB683918A publication Critical patent/GB683918A/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
    • C08G12/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08G12/263Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with at least two compounds covered by more than one of the groups C08G12/28 - C08G12/32
    • C08G12/266Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with at least two compounds covered by more than one of the groups C08G12/28 - C08G12/32 one being melamine

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)

Abstract

Melamine and formaldehyde are condensed under alkaline conditions and the condensation completed under acid conditions in presence of succinimide or a formaldehyde pre-condensate thereof and at least 4 mols. per mol. of melamine plus 1 mol. per mol. of succinimide of an aliphatic alcohol having 3-5 carbon atoms, the total proportion of formaldehyde and succinimide being 6.0-6.5 mols and 0.1-0.5 mols. respectively per mol. of melamine. Preferably, the melamine is condensed with formaldehyde in the first stage and the succinimide-formaldehyde condensate added at the beginning of the second stage. In example (1) 1 mol. melamine was dissolved in 6 mols. aqueous formaldehyde, the pH adjusted to 8-8.5 and the mixture boiled. 6-8 mols. of butanol and a solution obtained by boiling 0.5 mols. of succinimide with 0.5 mol. of neutral aqueous formaldehyde were then added and the pH adjusted with phosphoric acid to 5.5-6.5. Water was boiled off, butanol being condensed and returned to the mixture. The clear solution obtained could be diluted with butanol or an aromatic hydrocarbon. Example (2) is similar but all the formaldehyde is added in the first stage and succinimide itself in the second stage.
GB1435450A 1950-06-08 1950-06-08 Improvements in or relating to the production of melamine-formaldehyde condensation products Expired GB683918A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1435450A GB683918A (en) 1950-06-08 1950-06-08 Improvements in or relating to the production of melamine-formaldehyde condensation products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1435450A GB683918A (en) 1950-06-08 1950-06-08 Improvements in or relating to the production of melamine-formaldehyde condensation products

Publications (1)

Publication Number Publication Date
GB683918A true GB683918A (en) 1952-12-10

Family

ID=10039682

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1435450A Expired GB683918A (en) 1950-06-08 1950-06-08 Improvements in or relating to the production of melamine-formaldehyde condensation products

Country Status (1)

Country Link
GB (1) GB683918A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1004185B (en) * 1952-11-26 1957-03-14 Ciba Geigy Process for the preparation of polymerizable, amide-like compounds
US2808389A (en) * 1953-08-29 1957-10-01 Reichhold Chemicals Inc Process for the production of fusible alcohol-modified melamine resins, and resulting product

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1004185B (en) * 1952-11-26 1957-03-14 Ciba Geigy Process for the preparation of polymerizable, amide-like compounds
US2808389A (en) * 1953-08-29 1957-10-01 Reichhold Chemicals Inc Process for the production of fusible alcohol-modified melamine resins, and resulting product

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