GB703408A - Improvements in or relating to a process of making synthetic resins and the productsresulting therefrom - Google Patents

Improvements in or relating to a process of making synthetic resins and the productsresulting therefrom

Info

Publication number
GB703408A
GB703408A GB25486/50A GB2548650A GB703408A GB 703408 A GB703408 A GB 703408A GB 25486/50 A GB25486/50 A GB 25486/50A GB 2548650 A GB2548650 A GB 2548650A GB 703408 A GB703408 A GB 703408A
Authority
GB
United Kingdom
Prior art keywords
caustic soda
mixture
added
acid
etherifying
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
GB25486/50A
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.)
Standard Dyewood Co
Original Assignee
Standard Dyewood Co
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 Standard Dyewood Co filed Critical Standard Dyewood Co
Publication of GB703408A publication Critical patent/GB703408A/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
    • C08G8/28Chemically modified polycondensates
    • C08G8/36Chemically modified polycondensates by etherifying
    • 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
    • C08G8/18Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenols substituted by carboxylic or sulfonic acid groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)

Abstract

A synthetic resin is made by etherifying at least one phenolic hydroxyl group of a natural catechol tanning agent with mono-chloro or -bromo-acetic or propionic acid, by reaction in an alkaline medium with not more than 2 mols. of the acid per mol of the tanning agent, condensing the product thus formed with formaldehyde, and thereafter etherifying at least one of the remaining phenolic hydroxyl groups by reaction with an aralkyl halide in an alkaline aqueous medium. The natural tanning agents specified are quebracho extract, wattle, cutch and mangrove. Benzyl chloride is the preferred aralkyl chloride. In the example monochloracetic acid is added to a cooled mixture of quebracho extract and aqueous caustic soda followed by heating of the mix to 90-95 DEG C. for 1/2 hour. To this solution, after cooling, is added further caustic soda and aqueous formaldehyde, the mixture being heated, but cooled again for the addition of benzyl chloride and thereafter heated. A solution of caustic soda and sodium hydrosulphite is added to the mixture and the whole mass, while still hot, is poured into trays and solidified. The free resin may be obtained by acidification with, e.g. hydrochloric or sulphuric acid. The resins, which are soluble in alkalis and solvents such as benzene, toluene, methanol, ethanol and propanol, may be used for making compositions for coating, e.g. leather, cloth and paper, as disclosed in Specification 703,409. Specification 703,407 also is referred to.
GB25486/50A 1950-07-14 1950-10-19 Improvements in or relating to a process of making synthetic resins and the productsresulting therefrom Expired GB703408A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US703408XA 1950-07-14 1950-07-14

Publications (1)

Publication Number Publication Date
GB703408A true GB703408A (en) 1954-02-03

Family

ID=22094695

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25486/50A Expired GB703408A (en) 1950-07-14 1950-10-19 Improvements in or relating to a process of making synthetic resins and the productsresulting therefrom

Country Status (1)

Country Link
GB (1) GB703408A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997002216A1 (en) * 1995-07-06 1997-01-23 Betzdearborn Inc. Treatment of aqueous systems using a chemically modified tannin

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997002216A1 (en) * 1995-07-06 1997-01-23 Betzdearborn Inc. Treatment of aqueous systems using a chemically modified tannin
US5830315A (en) * 1995-07-06 1998-11-03 Betzdearborn Inc. Treatment of Aqueous systems using a chemically modified tannin
US5843337A (en) * 1995-07-06 1998-12-01 Betzdearborn Inc. Treatment of aqueous systems using a chemically modified tannin
US5977287A (en) * 1995-07-06 1999-11-02 Betzdearborn Inc. Treatment of aqueous systems using a chemically modified tannin

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