GB621542A - Improvements in the manufacture of varnish resin interpolymers - Google Patents

Improvements in the manufacture of varnish resin interpolymers

Info

Publication number
GB621542A
GB621542A GB4561/47A GB456147A GB621542A GB 621542 A GB621542 A GB 621542A GB 4561/47 A GB4561/47 A GB 4561/47A GB 456147 A GB456147 A GB 456147A GB 621542 A GB621542 A GB 621542A
Authority
GB
United Kingdom
Prior art keywords
styrene
oil
mixture
resins
methyl styrene
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
GB4561/47A
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.)
Dow Chemical Co
Original Assignee
Dow Chemical 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 Dow Chemical Co filed Critical Dow Chemical Co
Publication of GB621542A publication Critical patent/GB621542A/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
    • C08F212/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02Monomers containing only one unsaturated aliphatic radical
    • C08F212/04Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06Hydrocarbons
    • C08F212/08Styrene
    • 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
    • C08F242/00Copolymers of drying oils with other monomers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D125/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Coating compositions based on derivatives of such polymers
    • C09D125/02Homopolymers or copolymers of hydrocarbons
    • C09D125/04Homopolymers or copolymers of styrene
    • C09D125/08Copolymers of styrene
    • C09D125/14Copolymers of styrene with unsaturated esters
    • 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
    • C08F212/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02Monomers containing only one unsaturated aliphatic radical
    • C08F212/04Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06Hydrocarbons
    • C08F212/12Monomers containing a branched unsaturated aliphatic radical or a ring substituted by an alkyl radical

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Graft Or Block Polymers (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

A varnish resin is prepared by heating a mixture of (1) from 30 to 90 per cent by weight of a drying oil, free acid of a drying oil, or synthetic ester of a drying oil acid, which has a degree of conjugation not substantially exceeding that of dehydrated castor oil, and (2) from 70 to 10 per cent of a mixture of a polymerizable monovinyl aromatic compound and a nuclear alpha-methylene-lower alkyl aromatic compound, the alpha-methylene-lower alkyl group containing 3 or 4 carbon atoms and the mixture containing 50-80 per cent by weight of the monovinyl compound, to effect interpolymerization. Suitable drying oils are dehydrated castor oil, linseed, soyabean, perilla and fish oils. A mixture of one of these oils with a smaller proportion of a highly conjugated oil, e.g. tung oil, may be used. The monovinyl aromatic compound is preferably styrene, but o- and p-methyl styrene, o- and p-ethyl styrene, o-p-dimethyl styrene, p-chlorostyrene, p-methoxy styrene and vinyl naphthalene may be employed. Suitable alphamethylene-lower alkyl aromatic compounds are a -methyl styrene, p-methyl a -methyl styrene, a -ethyl styrene and p-chloro-a -methyl styrene. Polymerization may be effected by heating the mixture below boiling, e.g. 120-160 DEG C., with or without a catalyst such as benzoyl peroxide, acetyl benzoyl peroxide, tertiary butyl perbenzoate and tert.-butyl hydroperoxide. Alternatively, the drying oil is first heated to the polymerization temperature and the mixture of styrene or derivative and a -methyl styrene or derivative and catalyst is then added slowly over a period of several hours. Polymerization may also be effected in aqueous emulsion or in solution in, for example, diethyl benzene. The viscosity and hardness of the resins may be increased by heating at a temperature above 250 DEG C., but below their decomposition temperature, e.g. 275-295 DEG C. The resins are soluble in aromatic and aliphatic solvents and are compatible with linseed oil, most phenolic resins, some modified alkyd resins, rosin - esters, paracoumarone - indene, urea and melamine resins. The examples describe varnishes comprising the resins dissolved in mineral spirits/xylene and mineral spirits/toluene mixtures, with cobalt and manganese naphthenate driers and in one case containing guaiacol to prevent skinning; and an enamel made by adding titanium dioxide.
GB4561/47A 1944-09-26 1947-02-17 Improvements in the manufacture of varnish resin interpolymers Expired GB621542A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US649115XA 1944-09-26 1944-09-26

Publications (1)

Publication Number Publication Date
GB621542A true GB621542A (en) 1949-04-11

Family

ID=22059072

Family Applications (2)

Application Number Title Priority Date Filing Date
GB4561/47A Expired GB621542A (en) 1944-09-26 1947-02-17 Improvements in the manufacture of varnish resin interpolymers
GB33486/47A Expired GB649115A (en) 1944-09-26 1947-12-18 Improvements in or relating to the manufacture of varnish resin interpolymers

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB33486/47A Expired GB649115A (en) 1944-09-26 1947-12-18 Improvements in or relating to the manufacture of varnish resin interpolymers

Country Status (1)

Country Link
GB (2) GB621542A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE899863C (en) * 1949-08-26 1953-12-17 Kurt Herbert & Co Vorm Otto Lo Process for the production of copolymers

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE977088C (en) * 1951-07-02 1965-01-28 Burkhard Carlsohn Process for the preparation of polymerization products

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE899863C (en) * 1949-08-26 1953-12-17 Kurt Herbert & Co Vorm Otto Lo Process for the production of copolymers

Also Published As

Publication number Publication date
GB649115A (en) 1951-01-17

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