GB1023291A - Polymeric products and coating compositions containing the same - Google Patents

Polymeric products and coating compositions containing the same

Info

Publication number
GB1023291A
GB1023291A GB5082163A GB5082163A GB1023291A GB 1023291 A GB1023291 A GB 1023291A GB 5082163 A GB5082163 A GB 5082163A GB 5082163 A GB5082163 A GB 5082163A GB 1023291 A GB1023291 A GB 1023291A
Authority
GB
United Kingdom
Prior art keywords
allyl alcohol
water
adducts
styrene
copolymer
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
GB5082163A
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.)
Monsanto Co
Original Assignee
Monsanto 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 Monsanto Co filed Critical Monsanto Co
Publication of GB1023291A publication Critical patent/GB1023291A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/44Preparation of metal salts or ammonium salts
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F291/00Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/14Esterification

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)
  • Paints Or Removers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

An adduct of (a) an alpha, beta ethylenically unsaturated carboxylic acid, anhydride, or partial ester thereof containing the structure <FORM:1023291/C3/1> and (b) an ester of a copolymer of a styrene monomer and an allyl alcohol monomer which has the structure of a co-reaction product of 0.75 to 1.25 carboxyl equivalents of unsaturated fatty acids, rosin acids or mixtures thereof having an iodine unsaturation number by the ASTM D1467-57T test method of from 50 to 220, and 1.0 hydroxyl equivalents of a copolymer of a styrene monomer and an allyl alcohol monomer may be prepared by heating the reactants together at a temperature from 50 DEG C. to the reflux temperature of the system. The adduct may be formed in the presence of not more than 2% by weight of iodine (based on the reactants) and if desired, in the presence of a solvent. Lists of components (a), styrene monomers, allyl alcohol monomers, unsaturated fatty acids and rosin acids are given. The adducts may be employed in coating compositions such as paints by rendering the adducts water-soluble and then converting them into aqueous systems. The adducts may be made water-soluble by forming their salts by treatment with an alkali metal base, ammonia or an amine preferably in the presence of water and a water-miscible organic co-solvent. Lists of bases &c. and co-solvents are given. In the examples an adduct is prepared from a soya fatty acid ester of a styrene-allyl alcohol copolymer and maleic or fumaric acid either in the presence or absence of iodine. Coating compositions are formed from the ethylamine, ammonium or sodium salts of such adducts, the pigments and fillers added being selected from titanium dioxide, magnesium silicate, red iron oxide, lithopone and barytes.ALSO:Surfaces, e.g. metals, brick, ceramics, wood, plaster, paper, leather, plastics, are coated with a solution in an organic or aqueous solvent medium of an adduct of (a) an a ,b -ethylenically unsaturated carboxylic acid, anhydride or partial ester thereof containing the structure <FORM:1023291/B1-B2/1> and (b) an ester of a copolymer of a styrene monomer and an allyl alcohol monomer which has the structure of a co-reaction product of 0,75-1,25 carboxyl equivalents of unsaturated fatty acids, rosin acids or mixtures thereof having an iodine unsaturation number by the ASTM D1467-57T test method of from 50-220, and 1,0 hydroxyl equivalents of a copolymer of a styrene monomer and an allyl alcohol monomer. The coating compositions are produced by rendering the adducts water-soluble by treatment with alkali metal bases, ammonia or amines, and then converting them into aqueous systems. In the examples ammonium, sodium and monoethylamine salts of maleinized or fumarized soya fatty acid esters of styrene-allyl alcohol copolymers in aqueous systems are pigmented with one of the following: titanium dioxide, red iron oxide and lithopone, if desired in the presence of magnesium silicate or barytes and the mixture after blending with a cobalt drier and defoaming agent, water and organic solvents, is applied to steel plates and panels. An enamel top coat may be applied.
GB5082163A 1962-12-31 1963-12-24 Polymeric products and coating compositions containing the same Expired GB1023291A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US24821162A 1962-12-31 1962-12-31
US24829462A 1962-12-31 1962-12-31

Publications (1)

Publication Number Publication Date
GB1023291A true GB1023291A (en) 1966-03-23

Family

ID=26205132

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5082163A Expired GB1023291A (en) 1962-12-31 1963-12-24 Polymeric products and coating compositions containing the same

Country Status (3)

Country Link
BE (1) BE641932A (en)
FR (1) FR1401204A (en)
GB (1) GB1023291A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112933668A (en) * 2021-02-24 2021-06-11 江苏四新界面剂科技有限公司 Polyether defoaming agent for power plant desulfurization

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112933668A (en) * 2021-02-24 2021-06-11 江苏四新界面剂科技有限公司 Polyether defoaming agent for power plant desulfurization

Also Published As

Publication number Publication date
BE641932A (en) 1964-04-16
FR1401204A (en) 1965-06-04

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