GB520828A - Improvements in and relating to the production of aqueous compositions comprising thermo-setting resins and to the applications thereof - Google Patents

Improvements in and relating to the production of aqueous compositions comprising thermo-setting resins and to the applications thereof

Info

Publication number
GB520828A
GB520828A GB22986/38A GB2298638A GB520828A GB 520828 A GB520828 A GB 520828A GB 22986/38 A GB22986/38 A GB 22986/38A GB 2298638 A GB2298638 A GB 2298638A GB 520828 A GB520828 A GB 520828A
Authority
GB
United Kingdom
Prior art keywords
sodium hydroxide
per cent
phenol
reaction
xylenol
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
GB22986/38A
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.)
JAMES VICTOR NEVIN
Original Assignee
JAMES VICTOR NEVIN
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 JAMES VICTOR NEVIN filed Critical JAMES VICTOR NEVIN
Publication of GB520828A publication Critical patent/GB520828A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/46Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/47Condensation polymers of aldehydes or ketones
    • D21H17/48Condensation polymers of aldehydes or ketones with phenols
    • 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
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/04Condensation polymers of aldehydes or ketones with phenols only of aldehydes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Phenolic Resins Or Amino Resins (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

520,828. Phenol-aldehyde resins. NEVIN, J. V. Aug. 3, 1938, No. 22986. Convention date, Aug. 11, 1937. [Class 2 (iii)] Cresols, xylenols, or both, are reacted with an aldehyde, e.g., formaldehyde, in the presence of triethanolamine and of at least 10 per cent. of sodium hydroxide (or an equivalent amount of other alkali) calculated on the weight of cresol and xylenol to obtain a partial condensate, when the reaction is arrested by addition of water or alcohol containing at least 6 per cent. of sodium hydroxide (or the equivalent thereof) and cooling the mixture. There may also be present other hydroxy-aromatic compounds, e.g., phenol, resorcinol, hydroquinone, or #-naphthol; gums, e.g., gum accroides; and dispersing agents. In examples: hydroquinone, phenol, xylenol, and cresylic acid, or #-naphthol and cresylic acid, are reacted with formaldehyde solution in the presence of triethanolamine and of 13.3 per cent. of sodium hydroxide, the reaction being arrested by addition of a dilute aqueous solution of 8 per cent. of sodium hydroxide. The solutions may be used for coating or impregnating, or as binders for fibre board or plywood. U.S.A. Specifications 2,068,759 and 2,068,926 are referred to. According to the Specification as open to inspection under Sect. 91, oleic acid may also be present during the reaction. In examples: xylenol, or cresylic acid with or without resorcinol, phenol, or gum accroides, and formaldehyde are reacted in the presence of oleic acid, triethanolamine, and 10 per cent. of sodium hydroxide the reaction being arrested by a dilute aqueous solution of 6 per cent. of sodium hydroxide. This subject-matter does not appear in the Specification as accepted.
GB22986/38A 1937-08-11 1938-08-03 Improvements in and relating to the production of aqueous compositions comprising thermo-setting resins and to the applications thereof Expired GB520828A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US520828XA 1937-08-11 1937-08-11

Publications (1)

Publication Number Publication Date
GB520828A true GB520828A (en) 1940-05-06

Family

ID=21975348

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22986/38A Expired GB520828A (en) 1937-08-11 1938-08-03 Improvements in and relating to the production of aqueous compositions comprising thermo-setting resins and to the applications thereof

Country Status (1)

Country Link
GB (1) GB520828A (en)

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