GB974900A - Isocyanurates and polymeric materials therefrom - Google Patents
Isocyanurates and polymeric materials therefromInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-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.
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)
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 |
-
1962
- 1962-05-30 GB GB2085462A patent/GB974900A/en not_active Expired
Cited By (8)
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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