GB974900A - Isocyanurates and polymeric materials therefrom - Google Patents

Isocyanurates and polymeric materials therefrom

Info

Publication number
GB974900A
GB974900A GB2085462A GB2085462A GB974900A GB 974900 A GB974900 A GB 974900A GB 2085462 A GB2085462 A GB 2085462A GB 2085462 A GB2085462 A GB 2085462A GB 974900 A GB974900 A GB 974900A
Authority
GB
United Kingdom
Prior art keywords
tris
aralkyl
aryl
carbon atoms
less
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
GB2085462A
Inventor
Alan James Becalick
Geoffrey Arthur Haggis
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 GB2085462A priority Critical patent/GB974900A/en
Publication of GB974900A publication Critical patent/GB974900A/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
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/26Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
    • 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
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/44Polyester-amides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

The invention comprises isocyanurates of formula <FORM:0974900/C1/1> wherein R, R1 and R11 each represents an alkyl group containing not less than three carbon atoms, an aryl, aralkyl, or a cycloalkyl group. They are prepared by reacting an alkyl (not less than three carbon atoms), aryl, aralkyl, or cycloalkyl chloroformate with a metal cyanate, such as sodium cyanate. A preferred range of temperature is 40 DEG to 150 DEG C. and a solvent, such as acetonitrile and butyrolactone, may be present. Examples describe the preparation of triscarbobutoxy and carbopropoxyisocyanurates. Polymers are prepared by condensation of the products with polyhydroxy, aminohydroxy, or polyamino compounds.ALSO:Isocyanurates of formula <FORM:0974900/C3/1> wherein R, R1 and R11 each represents an alkyl group containing not less than three carbon atoms, or an aryl aralkyl, or a cycloalkyl group (see Division C2) are reacted with at least one polyhydroxy, aminohydroxy or polyamino compound to form polymeric materials. Ethylene glycol, butane-1:4-diol, trimethylolpropane, polyethers e.g. polyethylene glycol, polypropylene glycol, oxypropylated glycerol, oxypropylated tolylenediamine-diamine, polyesters e.g. polyethylene and polydiethylene adipate, and resins such as adipic/phthalic and/or mixtures of polyols such as glycerol/diethylene glycol, ethanolamine, 6-aminohexan -1- ol, diethanolamine, hexamethylene diamine, m- and p-phenylenediamines, polyethyleneamine and amino-ended polyamides and polyureas may be used. The reaction may be by heating at between 100 DEG and 250 DEG C. and solvents, catalysts e.g. metal oxide, tetrabutyl titanate, and dibutyl tin dilaurate, and pigments, anti-oxidants, flame retarders and flow improvers may be present. Examples describe the reaction of tris-carbobutoxy and tris carbopropoxyisocyanurates with a polyester from hexantriol, phthalic anhydride and adipic acid, a butylated urea/formaldehyde resin, methyl isobutyl ketone, cyclohexanone, and diacetone alcohol.ALSO:Isocyanates of formula <FORM:0974900/B1-B2/1> wherein R, R1 and R11 each represents an alkyl group containing not less than three carbon atoms, or an aryl, aralkyl or a cycloalkyl group (see Division C2) are interacted with at least one polyhydroxy, amino hydroxy or polyamino compound to form a polymer which may be used as a coating composition. Tris-carbobutoxy and tris-carbopropoxy isocyanates with a polyester resin, a butylated urea formaldehyde resin, methyl isobutyl ketone cyclohexanone and diacetone alcohol may be applied to steel panels cured at 180 DEG C. for 30 minutes to form a hard coating.
GB2085462A 1962-05-30 1962-05-30 Isocyanurates and polymeric materials therefrom Expired GB974900A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2085462A GB974900A (en) 1962-05-30 1962-05-30 Isocyanurates and polymeric materials therefrom

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2085462A GB974900A (en) 1962-05-30 1962-05-30 Isocyanurates and polymeric materials therefrom

Publications (1)

Publication Number Publication Date
GB974900A true GB974900A (en) 1964-11-11

Family

ID=10152866

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2085462A Expired GB974900A (en) 1962-05-30 1962-05-30 Isocyanurates and polymeric materials therefrom

Country Status (1)

Country Link
GB (1) GB974900A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5336566A (en) * 1993-04-30 1994-08-09 Basf Corporation Tri-carbamate-functional crosslinking agents
US5373069A (en) * 1993-07-28 1994-12-13 Basf Corporation Curable carbamate-functional polymers
US5512639A (en) * 1993-07-28 1996-04-30 Basf Corporation Curable compositions containing carbamate-modified polyisocyanates
US5726857A (en) * 1996-02-22 1998-03-10 Cray Research, Inc. Apparatus and method for mounting edge connectors within a circuit module
FR2898905A1 (en) * 2006-03-24 2007-09-28 Rhodia Recherches & Tech Use of polyisocyanate composition to make thermally crosslinkable coating paints or varnishes for car bodywork parts, having polyisocyanate, polymer compound e.g. acrylic polymer and aminoplastic resin e.g. urea-formaldehyde

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5336566A (en) * 1993-04-30 1994-08-09 Basf Corporation Tri-carbamate-functional crosslinking agents
US5373069A (en) * 1993-07-28 1994-12-13 Basf Corporation Curable carbamate-functional polymers
US5512639A (en) * 1993-07-28 1996-04-30 Basf Corporation Curable compositions containing carbamate-modified polyisocyanates
US5726857A (en) * 1996-02-22 1998-03-10 Cray Research, Inc. Apparatus and method for mounting edge connectors within a circuit module
FR2898905A1 (en) * 2006-03-24 2007-09-28 Rhodia Recherches & Tech Use of polyisocyanate composition to make thermally crosslinkable coating paints or varnishes for car bodywork parts, having polyisocyanate, polymer compound e.g. acrylic polymer and aminoplastic resin e.g. urea-formaldehyde
WO2007122309A1 (en) * 2006-03-24 2007-11-01 Rhodia Recherches Et Technologies Polyisocyanate composition with improved anti-shock properties
CN101454414B (en) * 2006-03-24 2012-08-29 罗地亚管理公司 Composition polyisocyanate a proprietes anti-chocs ameliorees
US8318310B2 (en) 2006-03-24 2012-11-27 Perstorp France Polyisocyanate coating compositions cross-linkable into enhanced anti-shock coatings

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