GB946365A - Composite structures - Google Patents

Composite structures

Info

Publication number
GB946365A
GB946365A GB4255761A GB4255761A GB946365A GB 946365 A GB946365 A GB 946365A GB 4255761 A GB4255761 A GB 4255761A GB 4255761 A GB4255761 A GB 4255761A GB 946365 A GB946365 A GB 946365A
Authority
GB
United Kingdom
Prior art keywords
polyurethane
substrate
ethylene
prepared
melamine
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
GB4255761A
Inventor
Maurice Sugden Magson
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB4255761A priority Critical patent/GB946365A/en
Publication of GB946365A publication Critical patent/GB946365A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin

Landscapes

  • Laminated Bodies (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

Composite structures or laminates comprising a metal (steel, tin, aluminium) or plastic (polyvinylchloride, polymethylmethacrylate, polyethylene, polystyrene, melamine- or ureaformaldehyde resin) substrate are prepared by a process comprising precoating the substrate with a solution in a halogenated aliphatic hydrocarbon solvent of resinous composition comprising a methacrylic acid, methacrylate or substituted methacrylate polymer or copolymer, a urea- or melamine-formaldehyde resin, an alkyd resin based on drying or non-drying oils or blends thereof, and then forming the polyurethane (e.g. foamed) in situ. Suitable solvents are trichloro ethylene, perchloroethylene, methylene dichloride, ethylene dichloride, chloroform, carbon tetrachloride and trichlorotrifluoromethane. The substrate which may be in the form of a sheet or box, may be degreased and roughened with abrasives before being coated with the resinous composition and heated before and after the polyurethane-forming composition is applied. The polyurethane may be prepared from polyester, polyesteramides or polyethers and organic polyisocyanates optionally in the presence of water and/or a liquid boiling below 75 DEG C. The polyesters and polyesteramides may be prepared from succinic, glutaric, adipic, suberic, acelaic, sebacic, phthalic, isophthalic and terephthalic acids, and ethylene glycol, 1,2 propylene glycol, butylene glycols, diethylene glycol, glycerol, trimethylol propane and pentaerythritol and, as necessary, ethylene diamine, hexamethylene diamine and monoethanolamine. The polyethers may be linear or branched and may be prepared from ethylene oxide, 1,2 butylene oxide, 2,3 butylene oxide, oxacyclobutane, substituted oxycylobutanes and tetrahydrofuran in the presence of a basic catalyst and water or glycerol, hexane triols, sorbitol, sucrose, pentaerythritol, triethanolamine, ethylene diamine, 2:4 and 2:6 totylene diamines, 2:4:6 tolylene triamine, 4:41-diamino diphenylmethane or triethylene tetramine. Polyisocyanates mentioned are 2:4 and 2:6 tolylene diisocyanate, hexamethylene diisocyanate, 2:4:6 toluene triisocyanate, 4:41 diisocyanato diphenylmethane and 3-methyl-4:41 diisocyanato diphenylmethane. The liquids boiling below 75 DEG C. mentioned are monofluorotrichloromethane, dibromo - difluoromethane, 1:1:2-trichloro-1:2:2-trifluoroethane, dichlorodifluoromethane and dichloromonofluoromethane. In the examples the substrate is precoated with (Examples 1, 2, 3, 4, 6 and 7) a solution of polymethacrylate copolymers in trichloroethylene and (Example 5) a solution of urea-formaldehyde and drying oil-based alkyd resins in trichloroethylene, and the polyurethane foam forming compositions are prepared from (Examples 1, 2, 3 and 5) a reaction product of 2:4, 2:6 tolylene diamines and propylene oxide, trichloromonofluoromethane, tri (b -chloroethyl) phosphate, polysiloxane-polyoxyalkylene block copolymer, dibutyltin dilaurate and diisocyanato diphenylmethane; (Example 4) as in Example 1 with glycerol present; (Example 6) a reaction product of triethanolamine and propylene oxide, water, tri -(b -chloroethyl) phosphate, triethanolamine, ethylene/propylene oxide block copolymer and diisocyanato diphenyl methane; (Example 7) as in Example 6 with trichloro monofluoromethane present.ALSO:Composite structures or laminates comprising a metal (steel, tin, aluminium) or plastic (polyvinylchloride, polymethylmethacrylate, polyethylene, polystyrene, melamine- or ureaformaldehyde resin) substrate are prepared by a process comprising precoating (brushing, spraying, dipping) the substrate with a solution in a halogenated aliphatic hydrocarbon solvent of a resinous composition comprising a methacrylic acid, methacrylate or substituted methacrylate polymer or copolymer, a urea- or melamine-formaldehyde resin, an alkyd resin based on drying or non-drying oils or blends thereof, and then forming the polyurethane in situ. Suitable solvents are trichloroethylene, perchloroethylene, methylene dichloride, ethylene dichloride, chloroform, carbon tetrachloride and trichlorotrifluoromethane. The polyurethane may be foamed, rigid, semi-rigid or flexible. The substrate which may be in the form of a sheet or box, may be degreased and roughened with abrasives before being coated with the resinous composition and heated before and after the polyurethane is applied.
GB4255761A 1961-11-28 1961-11-28 Composite structures Expired GB946365A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4255761A GB946365A (en) 1961-11-28 1961-11-28 Composite structures

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4255761A GB946365A (en) 1961-11-28 1961-11-28 Composite structures

Publications (1)

Publication Number Publication Date
GB946365A true GB946365A (en) 1964-01-15

Family

ID=10424950

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4255761A Expired GB946365A (en) 1961-11-28 1961-11-28 Composite structures

Country Status (1)

Country Link
GB (1) GB946365A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3490971A (en) * 1965-09-03 1970-01-20 Dow Chemical Co Foamable layer and method of applying same to substrate
EP1088114B1 (en) * 1998-06-15 2003-08-06 Dsm N.V. A composite material comprising a substrate with a barrier layer

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3490971A (en) * 1965-09-03 1970-01-20 Dow Chemical Co Foamable layer and method of applying same to substrate
EP1088114B1 (en) * 1998-06-15 2003-08-06 Dsm N.V. A composite material comprising a substrate with a barrier layer
US6632519B1 (en) 1998-06-15 2003-10-14 Dsm N.V. Composite material comprising a substrate and a barrier layer applied to the substrate
US6893679B2 (en) 1998-06-15 2005-05-17 Dsm N.V. Process for preparing a composite material by vapor depositing a barrier layer on a substrate

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