GB582448A - Improvements relating to the manufacture of synthetic resins - Google Patents

Improvements relating to the manufacture of synthetic resins

Info

Publication number
GB582448A
GB582448A GB505244A GB505244A GB582448A GB 582448 A GB582448 A GB 582448A GB 505244 A GB505244 A GB 505244A GB 505244 A GB505244 A GB 505244A GB 582448 A GB582448 A GB 582448A
Authority
GB
United Kingdom
Prior art keywords
per cent
resorcinol
phenol
specified
formaldehyde
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
GB505244A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB505244A priority Critical patent/GB582448A/en
Publication of GB582448A publication Critical patent/GB582448A/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
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/04Condensation polymers of aldehydes or ketones with phenols only of aldehydes
    • C08G8/08Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
    • C08G8/20Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with polyhydric phenols

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)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

Permanently fusible dihydric-phenol-aldehyde resins are made by heating together a dihydric phenol and an aldehyde in the absence of an acidic or basic catalyst in the proportion of less than one mol. of aldehyde to one mol. of dihydric phenol, adding said catalyst when the preliminary condensation is substantially complete, continuing the heating, and dehydrating, e.g. to a water-content of less than 1 per cent, preferably .5-.75 per cent. Phenols specified are resorcinol, hydroquinone and catechol, and a portion thereof may be replaced by phenol, cresylic acid, or other monohydric phenol, e.g. in an amount of 20-25 per cent. Aldehydes specified are formaldehyde, propionaldehyde and furfuraldehyde. In an example, formaldehyde solution is added gradually to resorcinol in a steam-heated vessel, and after the initial reaction has subsided, oxalic acid is added, refluxing is resumed for a short time, and water is then distilled off. The preferred molecular ratio of formaldehyde to resorcinol is .9 : 1 and preferably greater than .5 : 1. Other catalysts specified are hydrochloric, sulphuric, citric and tartaric acids, ammonium chloride, sodium and potassium hydroxides and carbonates, trisodium phosphate, triethanolamine, aniline, azoxy-toluidine, ethylenediamine. The preferred amount of catalyst based on the weight of resorcinol is .1-.3 per cent if the resin is to be used for bonding abrasive articles, and .6 per cent for other purposes. Hardening agents specified are hexamethylene tetramine, the oxymethylenes, para formaldehyde, polymethylol phenols and polymethylol melamines. The products are used in the manufacture of laminated products from cloth, e.g. cotton, paper, asbestos, or wood, abrasive articles, moulded articles, cold-setting adhesives, coating compounds, impregnating and reinforcing compounds, and in the bonding of nylon, leather and synthetic rubber.
GB505244A 1944-03-17 1944-03-17 Improvements relating to the manufacture of synthetic resins Expired GB582448A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB505244A GB582448A (en) 1944-03-17 1944-03-17 Improvements relating to the manufacture of synthetic resins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB505244A GB582448A (en) 1944-03-17 1944-03-17 Improvements relating to the manufacture of synthetic resins

Publications (1)

Publication Number Publication Date
GB582448A true GB582448A (en) 1946-11-18

Family

ID=9788843

Family Applications (1)

Application Number Title Priority Date Filing Date
GB505244A Expired GB582448A (en) 1944-03-17 1944-03-17 Improvements relating to the manufacture of synthetic resins

Country Status (1)

Country Link
GB (1) GB582448A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115386323A (en) * 2022-09-06 2022-11-25 江西省永晟科技有限公司 Preparation method and application of novel phenolic resin adhesive

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115386323A (en) * 2022-09-06 2022-11-25 江西省永晟科技有限公司 Preparation method and application of novel phenolic resin adhesive

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