GB759863A - Improvements in polymeric materials and methods of preparing them - Google Patents

Improvements in polymeric materials and methods of preparing them

Info

Publication number
GB759863A
GB759863A GB397554A GB397554A GB759863A GB 759863 A GB759863 A GB 759863A GB 397554 A GB397554 A GB 397554A GB 397554 A GB397554 A GB 397554A GB 759863 A GB759863 A GB 759863A
Authority
GB
United Kingdom
Prior art keywords
methyl
epoxy
polymeric
vinyl
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
GB397554A
Inventor
Martin Eli Cupery
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 GB397554A priority Critical patent/GB759863A/en
Publication of GB759863A publication Critical patent/GB759863A/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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/32Epoxy compounds containing three or more epoxy groups
    • C08G59/3209Epoxy compounds containing three or more epoxy groups obtained by polymerisation of unsaturated mono-epoxy compounds

Landscapes

  • 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

Polymeric phosphates are prepared by reacting ortho-, meta- or pyro-phosphoric acid or a partial ester thereof with a polymeric epoxide which is a copolymer of an ethylenically-unsaturated epoxy compound and an acyclic ethylenically-unsaturated epoxy-free compound, the polymeric epoxide containing from 3 per cent to 60 per cent of polymerized epoxy monomer and from 97 per cent to 40 per cent of polymerized epoxy-free monomer, the phosphoric acid or partial ester thereof being used in an amount of at least 0.5 mol. per oxirane oxygen atom in the copolymer. The epoxy monomer may be allyl glycidyl ether, glycidyl methacrylate, 4-vinyl cyclohexene oxide, butadiene monoepoxide, glycidyl acrylate, vinyl glycidyl phthalate or allyl glycidyl maleate or phthalate. The epoxy-free monomer may be vinyl acetate or propionate, acrylic acid, methyl or ethyl acrylate, methyl, ethyl, n-propyl or n-butyl mechacrylate, acrylonitrile, methacrylonitrile, acrylamide, methacrylamide, vinyl chloride or fluoride, isobutylene, 1,3-butadiene, isoprene, 1,3 - butadiene, isopropenyl acetate, vinylidene chloride, methyl vinyl ether, acrolein or methyl vinyl ketone. The reaction is preferably effected in an inert solvent such as acetone or dioxane at a temperature below 100 DEG C. The reaction products are soluble in organic solvents such as acetone, and some are soluble in aqueous alkali metal hydroxides, ammonia or amines to form solutions of salts, from which other salts, such as those of aluminium and calcium, may be precipitated. The copper and mercury salts may be used as bactericides or fungicides. The polymeric phosphates may be used as textile sizes, for treating leather and in coating compositions, other ingredients of which may be organic solvents such as acetone, methyl isobutyl ketone and n-butyl alcohol, pigments such as titanium dioxide, carbon black, iron blues, phthalocyanine blues and greens, metal oxides and chromates, extenders such as talc, barytes and china clay, and other film-forming materials such as urea-formaldehyde, melamine-formaldehyde and alkyd resins.ALSO:Surfaces are coated with polymeric phosphates which are the reaction products of copolymers of ethylenically unsaturated epoxy monomers and ethylenically unsaturated epoxy-free monomers with a phosphoric acid (see Group IV(a)). A steel panel was coated with a 30 per cent solution in acetone of the reaction product of orthophosphoric acid and a copolymer of glycidyl methacrylate and methyl methacrylate, and then baked for 45 minutes at 280 DEG F. to form a clear hard film which protected the metal from rusting. A pigmented enamel prepared from 126 parts of the above polymeric phosphate, 251 parts of methyl isobutyl ketone, 35 parts of butyl alcohol, 100 parts of ethylene glycol monoethylether acetate and 100 parts of titanium dioxide was sprayed on a clean metal panel which was baked for 30 minutes at 300 DEG F. to produce a durable white glossy coating. Aqueous solutions of ammonium, amine or alkali metal salts of the polymeric phosphates may be used as clear finishes for wood, glass, ceramics, textiles, paper and metals and may be used either as primer-sealer coats for subsequent application of other finishes or as the total protective or decorative finish; cupric ammonium salts may be used for sealing wood, textile and paper surfaces.
GB397554A 1954-02-10 1954-02-10 Improvements in polymeric materials and methods of preparing them Expired GB759863A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB397554A GB759863A (en) 1954-02-10 1954-02-10 Improvements in polymeric materials and methods of preparing them

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB397554A GB759863A (en) 1954-02-10 1954-02-10 Improvements in polymeric materials and methods of preparing them

Publications (1)

Publication Number Publication Date
GB759863A true GB759863A (en) 1956-10-24

Family

ID=9768432

Family Applications (1)

Application Number Title Priority Date Filing Date
GB397554A Expired GB759863A (en) 1954-02-10 1954-02-10 Improvements in polymeric materials and methods of preparing them

Country Status (1)

Country Link
GB (1) GB759863A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2413450A1 (en) * 1977-12-27 1979-07-27 Ford France COATING COMPOSITION WITH A HIGH SOLID CONTENT
DE3009715A1 (en) * 1979-04-03 1980-10-16 Vianova Kunstharz Ag Primer filler binder - esp. for reverse process car lacquering, contains phosphoric- and/or phosphonic acid-modified epoxy! resin soln.
GB2179666A (en) * 1985-07-12 1987-03-11 Kao Corp Polymer having phosphate groups
US5478894A (en) * 1992-06-08 1995-12-26 Hoechst Celanese Corporation Process for preparing crosslinked water absorbent resins

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2413450A1 (en) * 1977-12-27 1979-07-27 Ford France COATING COMPOSITION WITH A HIGH SOLID CONTENT
DE3009715A1 (en) * 1979-04-03 1980-10-16 Vianova Kunstharz Ag Primer filler binder - esp. for reverse process car lacquering, contains phosphoric- and/or phosphonic acid-modified epoxy! resin soln.
GB2179666A (en) * 1985-07-12 1987-03-11 Kao Corp Polymer having phosphate groups
GB2179666B (en) * 1985-07-12 1989-10-25 Kao Corp Thickening aqueous electrolyte solutions with a polymer having phosphate groups
US5478894A (en) * 1992-06-08 1995-12-26 Hoechst Celanese Corporation Process for preparing crosslinked water absorbent resins

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