GB701441A - Improvements in or relating to the manufacture of styrene copolymers - Google Patents

Improvements in or relating to the manufacture of styrene copolymers

Info

Publication number
GB701441A
GB701441A GB13202/50A GB1320250A GB701441A GB 701441 A GB701441 A GB 701441A GB 13202/50 A GB13202/50 A GB 13202/50A GB 1320250 A GB1320250 A GB 1320250A GB 701441 A GB701441 A GB 701441A
Authority
GB
United Kingdom
Prior art keywords
oil
vinyl aromatic
meta
glycerol
per cent
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
GB13202/50A
Inventor
Frank Armitage
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.)
Lewis Berger and Sons Ltd
Original Assignee
Lewis Berger and Sons Ltd
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 Lewis Berger and Sons Ltd filed Critical Lewis Berger and Sons Ltd
Publication of GB701441A publication Critical patent/GB701441A/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
    • 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
    • C08F242/00Copolymers of drying oils with other monomers
    • 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
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/01Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
    • 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

Landscapes

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

Abstract

Copolymers are prepared by reacting together in the absence of a solvent for the reactants a vinyl aromatic compound and a polyhydric alcoholic ester as defined below in the presence of an activated silicate catalyst, the vinyl aromatic compound being used in an amount such as to provide a vinyl aromatic content in the copolymer of from 20 per cent. to 50 per cent. by weight. The vinyl aromatic compound may be styrene, para-methyl styrene, parachlorostyrene, para-fluorostyrene, meta-chlorostyrene, meta-fluorostyrene, meta and paratrichloromethylstyrene, meta- and para-trifluoromethylstyrene, methoxystyrene and vinyl naphthalene. The expression "polyhydric alcoholic ester" includes the ester or partial ester of a polyhydric alcohol such as glycerol, pentacrythritol, mannitol or sorbitol with an unsaturated fatty oil acid such as may be derived from drying and semi-drying oils of vegetable or animal origin, oil-modified alkyd resins made from polycarboxylic acids such as phthalic, maleic or adipic acid, and synthetic drying oils produced by esterification of isomerized drying oil fatty acids with polyhydric alcohols. Examples describe the copolymerization of styrene with mixtures of linseed oil and tung oil or with oil-modified alkyd resins prepared by reacting (a) castor oil, phthalic anhydride and glycerol; (b) phthalic anhydride, glycerol, linseed oil fatty acids and wood oil; or (c) castor oil, phthalic anhydride, glycerol, and linseed oil. The catalyst may be Fuller's earth, Tonsil, Attapulgus clay, bentonite, montmorillonite or a silicate gel. The catalyst may be used in an amount of from 1 per cent. to 5 per cent. by weight of the vinyl aromatic compound and the copolymerization may be effected at 70-200 DEG C. preferably 130-180 DEG C. Specification 524,156 is referred to.
GB13202/50A 1950-05-25 1950-05-25 Improvements in or relating to the manufacture of styrene copolymers Expired GB701441A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB294347X 1950-05-25
GB210551X 1951-05-21

Publications (1)

Publication Number Publication Date
GB701441A true GB701441A (en) 1953-12-23

Family

ID=26255078

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13202/50A Expired GB701441A (en) 1950-05-25 1950-05-25 Improvements in or relating to the manufacture of styrene copolymers

Country Status (6)

Country Link
BE (1) BE503484A (en)
CH (1) CH294347A (en)
DE (1) DE938628C (en)
FR (1) FR1050282A (en)
GB (1) GB701441A (en)
NL (1) NL161312B (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1975959A (en) * 1930-05-13 1934-10-09 Du Pont Polymerization of vinyl compounds in the presence of film forming materials
DE719674C (en) * 1937-07-18 1942-04-14 Ig Farbenindustrie Ag Process for the preparation of condensation products from aromatic vinyl compounds and aromatic oxy compounds or their alkyl ethers
US2366008A (en) * 1942-08-11 1944-12-26 Gen Electric Production of synthetic polymeric compositions comprising aminated polymerizates of poly-vinyl aryl compounds and treatment of liquid media therewith

Also Published As

Publication number Publication date
FR1050282A (en) 1954-01-06
CH294347A (en) 1953-11-15
NL161312B (en)
DE938628C (en) 1956-03-15
BE503484A (en)

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