GB984300A - Polyurethane foam product and method of making same - Google Patents

Polyurethane foam product and method of making same

Info

Publication number
GB984300A
GB984300A GB3641262A GB3641262A GB984300A GB 984300 A GB984300 A GB 984300A GB 3641262 A GB3641262 A GB 3641262A GB 3641262 A GB3641262 A GB 3641262A GB 984300 A GB984300 A GB 984300A
Authority
GB
United Kingdom
Prior art keywords
foam
polyisocyanate
stiffened
organic
coated
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
GB3641262A
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.)
NORMAN HENRY STARK
Original Assignee
NORMAN HENRY STARK
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 NORMAN HENRY STARK filed Critical NORMAN HENRY STARK
Publication of GB984300A publication Critical patent/GB984300A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/36After-treatment
    • C08J9/40Impregnation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Laminated Bodies (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

Open-cell polyurethane foams are stiffened by impregnating the foam in an organic polyisocyanate or solution of organic polyisocyanate and thereafter drying the product. The foam may be first impregnated with a weakening agent, e.g. caustic soda and mechanically worked to weaken its cell wall structure. The product may have a density in the range 0.75-2.4 pounds per cubic foot, and may be coated after stiffening with an organic coating composition, e.g. resins, waxes or rubbers which covers the internal and external cell surfaces. At least one defined region of the foam may have a rigidity substantially in excess of that of the remainder, obtained by restricting the action of the polyisocyanate to a defined region of the foam by masking. Preferred polyisocyanates are arylene diisocyanates, e.g. the toluene diisocyanates. After treatment any excess polyisocyanate may be removed by evaporation at 20-40 DEG C. or by heating to 160 DEG F. or reduced pressure. Plasticizers, e.g. cresyl diphenyl phosphate, tricresyl phosphate; dibutyl phthalate; di-(2-ethyl hexyl)phthalate; diethyl, dibutyl and polypropyl adipates may be added to the polyisocyanate. Solvents may be aliphatic hydrocarbons, chlorinated hydrocarbons, ketones and aromatic hydrocarbons. In examples, polyurethane foams derived from polyethers and polyesters were repeatedly compressed in polyisocyanates at room temperature for 1-5 minutes and were then airdried.ALSO:Polyurethane foams (which have been stiffened by immersion in an organic polyisocyanate followed by drying (see Division C3), are coated on their internal and external cell surfaces with an organic material, e.g. ethyl or nitro cellulose, chlorinated rubber, and coumarone, epoxy, polyethylene, fluoroethylene, furan, melamine, phenolformaldehyde and hydrocarbon resins, also synthetic rubbers, silicones, urea formaldehyde resins and polymers of styrene, vinyl chloride, vinyl chloridevinyl acetate, terpenes and waxes. The coating compositions are applied to the stiffened foam by immersing the foam in a solvent containing the coating composition and compressing and decompressing till saturation occurs. Plasticizers may be included in the coating composition. In an example a stiffened polyurethane foam was coated with a solution of a polyvinyl chloride-polyvinyl acetate copolymer in tetrahydrofuran.
GB3641262A 1961-12-13 1962-09-25 Polyurethane foam product and method of making same Expired GB984300A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US15915661A 1961-12-13 1961-12-13

Publications (1)

Publication Number Publication Date
GB984300A true GB984300A (en) 1965-02-24

Family

ID=22571318

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3641262A Expired GB984300A (en) 1961-12-13 1962-09-25 Polyurethane foam product and method of making same

Country Status (2)

Country Link
DE (1) DE1224033B (en)
GB (1) GB984300A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2490659A1 (en) * 1980-09-01 1982-03-26 Wako Chem IMPREGNATION PRODUCT FOR THE MANUFACTURE OF RIGID OR SEMI-RIGID RESIN FOAMS
EP0276465A2 (en) * 1987-01-07 1988-08-03 BASF Aktiengesellschaft Process for producing light flat articles using aqueous dispersions or emulsions of organic compounds containing NCO groups, and the articles thus prepared
GB2249738A (en) * 1990-11-13 1992-05-20 Aaron Sherman Foamed products
DE10129858A1 (en) * 2001-06-21 2003-01-09 Hp Chem Pelzer Res & Dev Ltd Surface coating of acoustically effective foam materials

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE957294C (en) * 1953-01-03 1957-01-31 Bayer Ag Process for coating or preparing carrier materials
US2900278A (en) * 1956-06-15 1959-08-18 Scott Paper Co Cellular product and method of making the same
US2926398A (en) * 1958-02-03 1960-03-01 Mandel Henri Window raising mechanism with controlling planetary gear train

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2490659A1 (en) * 1980-09-01 1982-03-26 Wako Chem IMPREGNATION PRODUCT FOR THE MANUFACTURE OF RIGID OR SEMI-RIGID RESIN FOAMS
EP0276465A2 (en) * 1987-01-07 1988-08-03 BASF Aktiengesellschaft Process for producing light flat articles using aqueous dispersions or emulsions of organic compounds containing NCO groups, and the articles thus prepared
EP0276465A3 (en) * 1987-01-07 1989-12-20 Basf Aktiengesellschaft Process for producing light flat articles using aqueous dispersions or emulsions of organic compounds containing nco groups, and the articles thus prepared
GB2249738A (en) * 1990-11-13 1992-05-20 Aaron Sherman Foamed products
GB2249738B (en) * 1990-11-13 1995-07-05 Aaron Sherman Foamed products
DE10129858A1 (en) * 2001-06-21 2003-01-09 Hp Chem Pelzer Res & Dev Ltd Surface coating of acoustically effective foam materials

Also Published As

Publication number Publication date
DE1224033B (en) 1966-09-01

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