GB608940A - Improvements in or relating to resin products and preparations thereof - Google Patents

Improvements in or relating to resin products and preparations thereof

Info

Publication number
GB608940A
GB608940A GB25017/44A GB2501744A GB608940A GB 608940 A GB608940 A GB 608940A GB 25017/44 A GB25017/44 A GB 25017/44A GB 2501744 A GB2501744 A GB 2501744A GB 608940 A GB608940 A GB 608940A
Authority
GB
United Kingdom
Prior art keywords
phenol
formaldehyde
per cent
parts
product
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
GB25017/44A
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.)
Hexion Inc
Original Assignee
Borden Inc
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 Borden Inc filed Critical Borden Inc
Publication of GB608940A publication Critical patent/GB608940A/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
    • C08G8/24Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with mixtures of two or more phenols which are not covered by only one of the groups C08G8/10 - C08G8/20

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

A water-soluble resin is made by reacting one mol. of phenol with 1.3-2.5 mols. of formaldehyde at a pH of 7.5-8.5 in presence of a nonvolatile alkali catalyst until the reaction product contains less than 2 per cent free formaldehyde and tolerates the addition of from 0.1 to 5 volumes of water without causing the resulting solution to become cloudy at 70 DEG F., and reacting the resulting product of said first reaction with 10-150 parts by weight of an unsubstituted mononuclear dihydric phenol for each 100 parts phenol until the condensation product has a viscosity in aqueous media of A to G on the Gardner scale. The product may be vacuum distilled until it has a viscosity of 120-135 revolutions per minute at 70 DEG F. in a Stormer viscometer using a 500-gram weight. Further alkali (which may be volatile) may be added with the dihydric phenol according to the pH required in the final product. A part of the dihydric phenol, up to 10 per cent by weight of the phenol, may be added to the phenol-formaldehyde mixture before the preliminary condensation. The percentage of free formaldehyde at the end of the preliminary condensation is preferably less than 0.75 per cent, and the preferred proportion of formaldehyde used is 1.5-2.0 mols. per mol. of phenol. Cresols or xylenols may replace up to 10 per cent of the phenol. Alkaline catalysts specified are caustic soda and potash, sodium carbonate and trisodium phosphate. The amount of resorcinol added is preferably 75-150 parts per 100 parts phenol. The products may be used as glues or casting resins. Examples described the mixing and refluxing of phenol, 37 per cent formaldehyde solution, and caustic soda solution, followed by the addition of resorcinol and more caustic soda solution and heating to 80-90 DEG C., and vacuum distillation. Examples also describe the use of the products as casting resins, using hypophosphorous acid as catalyst, and acids specified as suitable for casting are formic, acetic, lactic, monochloracetic and monochlorpropionic.
GB25017/44A 1943-11-30 1944-12-13 Improvements in or relating to resin products and preparations thereof Expired GB608940A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US608940XA 1943-11-30 1943-11-30

Publications (1)

Publication Number Publication Date
GB608940A true GB608940A (en) 1948-09-23

Family

ID=22032397

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25017/44A Expired GB608940A (en) 1943-11-30 1944-12-13 Improvements in or relating to resin products and preparations thereof

Country Status (1)

Country Link
GB (1) GB608940A (en)

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