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GB642414A - Improvements in and relating to modified rosin esters and compositions containing them - Google Patents

Improvements in and relating to modified rosin esters and compositions containing them

Info

Publication number
GB642414A
GB642414A GB19527/47A GB1952747A GB642414A GB 642414 A GB642414 A GB 642414A GB 19527/47 A GB19527/47 A GB 19527/47A GB 1952747 A GB1952747 A GB 1952747A GB 642414 A GB642414 A GB 642414A
Authority
GB
United Kingdom
Prior art keywords
diallyl
abietate
maleate
rosin
ester
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
GB19527/47A
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.)
Montclair Research Corp
Original Assignee
Montclair Research Corp
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 Montclair Research Corp filed Critical Montclair Research Corp
Publication of GB642414A publication Critical patent/GB642414A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09FNATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
    • C09F1/00Obtaining purification, or chemical modification of natural resins, e.g. oleo-resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

Modified rosin esters are prepared by reacting at between 200 DEG and 300 DEG C., a rosin ester of a polyhydric alcohol containing the conjugated unsaturation of abietic acid with an unsaturated alcohol ester of either (a) an alpha unsaturated alpha beta dicarboxylic acid, or (b) a saturated dicarboxylic acid. The reaction is preferably carried out in two stages, first at 200-250 DEG C. and when a preliminary reaction is over, at 250-300 DEG C. Esters of allyl, crotyl, propargyl and butenyl alcohols are suitable, preferably allyl and di-allyl phthalates, succinates, maleates, and fumarates. The products may be copolymerized with styrene, methyl methacrylate, or vinyl acetate, and the copolymers made into drying oils to form varnishes, or they may be blended with urea-, phenol-, or melamine-formaldehyde resins cellulose derivatives, or methyl methacrylate, acrylate, vinylidene chloride resins or polyvinyl alcohol. The products may be cooked into drying oils to form varnish bases, which may be thinned with mineral spirits, and driers added. In an example (1) glycerol abietate and diallyl maleate are heated and the temperature increased slowly from 200-300 DEG C. The product is dissolved in heated linseed oil (previously treated to produce conjugated unsaturation). The mixture is dissolved in mineral spirits and lead and cobalt naphthenates added. Alternatively a lacquer is obtained by dissolving the resin in a mixture of rosin, nitrocellulose, xylol, butyl-, ethyl-, and amyl acetates, and octyl alcohol. The resin is also soluble in esters, ketones, hydrocarbons, chlorinated hydrocarbons, glycol ethers, nitropropane, and butanol. The product of a similar example (2) is saponified with sodium hydroxide. Further examples describe heating together mixtures of (3) pentaerythrityl abietate and diallyl maleate; (4) pentaerythrityl abietate and diallyl fumarate; (5) ester gum and diallyl fumarate; (6) ester gum and diallyl chloromaleate; (7) ester gum and diallyl itaconate; (8) ester gum and diallyl citraconate; (9) the reaction product of glycerol and rosin and monoallyl maleate; (10) the reaction product of rosin and pentaerythritol and monoallyl maleate; (11) the reaction product of tri-hydroxymethyl-amino-methane and rosin and monoallyl maleate; (12) the reaction product of rosin and glycerol and monoallyl citracontate; (13) ester gum, glycerol, and monomethallyl maleate. Examples using esters of saturated polycarboxylic acids describe reacting mixtures of (14) and (15) glyceryl tri-abietate and diallyl phthalate; (16) pentaerythrityl tetra-abietate and diallyl phthalate; (17) pentaerythrityl tetra-abietate and diallyl succinate; (18) glyceryl tri-abietate and diallyl oxalate; (19) glyceryl tri-abietate and diallyl adipate; (20) glyceryl tri-abietate and diallyl succinate; (21) glyceryl diabietate and monoallyl phthalate; (22) pentaerythrityl triabietate and monomethallyl phthalate; (23) tri-hydroxy methylamine methane triabietate and monomethallyl succinate. Varnish bases are described in further examples, in which the product obtained from a resin ester and an unsaturated alcohol ester is afterwards heated with drying oils. Materials employed are, in examples (24) and (25) rosin glyceride, diallyl maleate, and linseed oil; (26) pentaerythritol tetra-abietate, diallyl fumarate, linseed oil, and china-wood oil; (27) glycerol diabietate, monoallyl maleate and raw tung oil; (28) ester gum, glycerol, monomethallyl maleate, and dehydrated castor oil; (29) glyceryl abietate, diallyl maleate, and alkali-refined linseed oil; (30) the resin of (23) and linseed oil; (31) ester gum, diallyl phthalate, and linseed oil; (32) pentaerythrityl abietate, diallyl phthalate, and linseed oil. The base is in each case thinned with mineral spirits and lead and cobalt naphenate driers are added.
GB19527/47A 1944-04-14 1947-07-21 Improvements in and relating to modified rosin esters and compositions containing them Expired GB642414A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US642414XA 1944-04-14 1944-04-14

Publications (1)

Publication Number Publication Date
GB642414A true GB642414A (en) 1950-09-06

Family

ID=22054544

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19527/47A Expired GB642414A (en) 1944-04-14 1947-07-21 Improvements in and relating to modified rosin esters and compositions containing them

Country Status (1)

Country Link
GB (1) GB642414A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2757187A (en) * 1955-11-14 1956-07-31 Monsanto Chemicals Polycarboxylates
US3044998A (en) * 1958-11-13 1962-07-17 Standard Oil Co Borated monomers and polymers
US3182047A (en) * 1961-06-02 1965-05-04 Commerical Solvents Corp Amino alcohol modified polyacrylates
CN107964370A (en) * 2018-01-04 2018-04-27 广东华林化工有限公司 A kind of technology for producing colophony

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2757187A (en) * 1955-11-14 1956-07-31 Monsanto Chemicals Polycarboxylates
US3044998A (en) * 1958-11-13 1962-07-17 Standard Oil Co Borated monomers and polymers
US3182047A (en) * 1961-06-02 1965-05-04 Commerical Solvents Corp Amino alcohol modified polyacrylates
CN107964370A (en) * 2018-01-04 2018-04-27 广东华林化工有限公司 A kind of technology for producing colophony
CN107964370B (en) * 2018-01-04 2020-05-05 广东华林化工有限公司 Rosin production process

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