GB341012A - Improvement in synthetic resin - Google Patents

Improvement in synthetic resin

Info

Publication number
GB341012A
GB341012A GB2011429A GB2011429A GB341012A GB 341012 A GB341012 A GB 341012A GB 2011429 A GB2011429 A GB 2011429A GB 2011429 A GB2011429 A GB 2011429A GB 341012 A GB341012 A GB 341012A
Authority
GB
United Kingdom
Prior art keywords
acid
per cent
beta
solution
cobalt
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
GB2011429A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and 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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to GB2011429A priority Critical patent/GB341012A/en
Priority to FR678539D priority patent/FR678539A/en
Publication of GB341012A publication Critical patent/GB341012A/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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/46Polyesters chemically modified by esterification

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)

Abstract

Paints.--A modified alkyl resin prepared by esterifying a polyhydric alcohol with a polybasic acid and pure beta-eleostearic acid with or without a resin acid is used as a component of a paint or coating composition. In an example, a mixture of glycerol, phthalic anhydride, raw Congo gum and beta-eleostearic acid is heated gradually to 180 DEG C. and subsequently heated to 250 DEG C. for a short period; it is then cut hot in high flash-point solvent naphtha. In place of glycerol, other polyhydric alcohols may be used, such as glycol, mannitol, penta-erythritol; as examples of other polybasic acids, malic, succinic, camphoric, tartaric and citric acids are specified. A resin solution prepared according to the Example may have a liquid cobalt dryer incorporated to form a quick drying varnish. The liquid cobalt dryer may be a 10 per cent solution of cobalt linoleate in turpentine and may contain 0,75 per cent of cobalt as metal, based upon the weight of liquid dryer. Beta-eleostearic acid is prepared from china wood oil by treatment with ,03 to ,05 per cent by weight of iodine in a dilute alcoholic solution (2,5 to 5 per cent). The solution is allowed to stand until it has set to a substantially solid mass, usually for several days, then mixed with about one-third its weight of acetone and centrifuged to remove the liquid residue. The solid residue in the centrifugue is washed several times with acetone and a yield obtained of approximately 50 per cent of solid beta-eleostearin of the raw oil used. The acid is obtained by treating the beta-eleostearin with a solution of sodium hydroxide and subsequently treating the sodium eleostearate with dilute hydrochloric acid.ALSO:Ester condensation products.-A modified alkyd resin is prepared by esterifying a polyhydric alcohol with a polybasic acid and pure betaeleostearic acid with or without a resin acid. In an example, a mixture of glycerol, phthalic anhydride, raw Congo gum and betaeleostearic acid is heated gradually to 180 DEG C. and subsequently heated to 250 DEG C. for a short period. It is then cut hot in high flash-point solvent naphtha. In place of glycerol, other polyhydric alcohols may be used, such as glycol, mannitol, pentaerythritol; as examples of other polybasic acids, malic, succinic, camphoric, tartaric and citric acids are specified. A resin solution prepared according to the example may have a liquid cobalt dryer incorporated to form a quick drying varnish. The liquid cobalt dryer may be a 10 per cent solution of cobalt linoleate in turpentine and may contain 0,75 per cent of cobalt as metal, based upon the weight of liquid dryer. Beta-eleostearic acid is prepared from china wood oil by treatment with ,03 to ,05 per cent by weight of iodine in a dilute alcoholic solution (2,5 to 5 per cent). The solution is allowed to stand until it has set to a substantially solid mass, usually for several days, then mixed with about one-third its weight of acetone and centrifuged to remove the liquid residue. The solid residue in the centrifuge is washed several times with acetone and a yield obtained of approximately 50 per cent of solid beta-elaeostearin of the raw oil used. The acid is obtained by treating the beta-elaeostearin with a solution of sodium hydroxide and subsequently treating the sodium eleostearate with dilute hydrochloric acid.
GB2011429A 1929-07-01 1929-07-01 Improvement in synthetic resin Expired GB341012A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB2011429A GB341012A (en) 1929-07-01 1929-07-01 Improvement in synthetic resin
FR678539D FR678539A (en) 1929-07-01 1929-07-17 Synthetic resin enhancements

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2011429A GB341012A (en) 1929-07-01 1929-07-01 Improvement in synthetic resin

Publications (1)

Publication Number Publication Date
GB341012A true GB341012A (en) 1931-01-01

Family

ID=10140608

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2011429A Expired GB341012A (en) 1929-07-01 1929-07-01 Improvement in synthetic resin

Country Status (2)

Country Link
FR (1) FR678539A (en)
GB (1) GB341012A (en)

Also Published As

Publication number Publication date
FR678539A (en) 1930-03-25

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