GB1408165A - Toluene diisocyanate urethane lacquer solutions - Google Patents
Toluene diisocyanate urethane lacquer solutionsInfo
- Publication number
- GB1408165A GB1408165A GB5521872A GB5521872A GB1408165A GB 1408165 A GB1408165 A GB 1408165A GB 5521872 A GB5521872 A GB 5521872A GB 5521872 A GB5521872 A GB 5521872A GB 1408165 A GB1408165 A GB 1408165A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dmf
- toluene
- prepolymers
- isopropanol
- nov
- 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
- 239000004922 lacquer Substances 0.000 title abstract 3
- QOIMTORIVXGIHY-UHFFFAOYSA-N 2,4-diisocyanato-1-methylbenzene;ethyl carbamate Chemical compound CCOC(N)=O.CC1=CC=C(N=C=O)C=C1N=C=O QOIMTORIVXGIHY-UHFFFAOYSA-N 0.000 title 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 4
- 229920000728 polyester Polymers 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 2
- 229920000570 polyether Polymers 0.000 abstract 2
- 229920002635 polyurethane Polymers 0.000 abstract 2
- 239000004814 polyurethane Substances 0.000 abstract 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract 2
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 abstract 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 1
- 239000006096 absorbing agent Substances 0.000 abstract 1
- 235000011037 adipic acid Nutrition 0.000 abstract 1
- 239000001361 adipic acid Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000003963 antioxidant agent Substances 0.000 abstract 1
- 150000001565 benzotriazoles Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical class CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- -1 ethylene, tetramethylene, hexamethylene Chemical group 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 235000013772 propylene glycol Nutrition 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000011877 solvent mixture Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 abstract 1
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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
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)
- Paints Or Removers (AREA)
Abstract
1408165 Polyurethane lacquer WITCO CHEMICAL CORP 29 Nov 1972 [30 Nov 1971] 55218/72 Heading C3R A one-component polyurethane lacquer solution comprises a prepolymer of a linear OH- terminated polyether or polyester and toluene diisocyanate which has been chain extended with sufficient menthane and/or isophorone diamine to react completely with 80 to 96% of the available NCO groups, and also for polyester derived prepolymers (but only optionally for polyether-derived prepolymers) sufficient C 2-22 alkyl and/or cycloalkyl monoamines to react completely with up to 10% of the available NCO groups, such chain extended prepolymer being dissolved in a solvent mixture comprising at least 5 vol. per cent of a C 1-5 alkanol and such other inert organic solvents as may be required to produce a "balanced solution", i.e. wherein all the components remain in solution after all the ingredients have reacted. Antioxidants, e.g. dibutylated phenols, and U.V. absorbers, e.g. benzotriazoles, may be included. In specific prepolymers are used from poly-(1,2-oxypropylene) glycol, poly-(oxytetramethylene) glycol and polyesters of adipic acid with ethylene, tetramethylene, hexamethylene or a mixture of ethylene and propylene glycols; the monoamines used are mono- and di-butylamines, npropylamine, diethylamine and n-octadecylamine, and the solvent combinations are (by volume), MEU/ethanol/DMF, 80/15/5; toluene/ isopropanol/DMF, 65/20/15 and 70/25/5; MEK/ ethanol, 80/20; toluene/n-propanol/DMF, 70/ 20/10; and MFK/acetone/isopropanol/DMF, 40/40/10/10.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20348271A | 1971-11-30 | 1971-11-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1408165A true GB1408165A (en) | 1975-10-01 |
Family
ID=22754195
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5521872A Expired GB1408165A (en) | 1971-11-30 | 1972-11-29 | Toluene diisocyanate urethane lacquer solutions |
Country Status (8)
| Country | Link |
|---|---|
| JP (1) | JPS4864123A (en) |
| BE (1) | BE791999A (en) |
| CA (1) | CA979566A (en) |
| DE (1) | DE2257490A1 (en) |
| FR (1) | FR2162015B1 (en) |
| GB (1) | GB1408165A (en) |
| IT (1) | IT970240B (en) |
| NL (1) | NL7215813A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2139239A (en) * | 1983-05-03 | 1984-11-07 | Nl Industries Inc | Water soluble, modified polyurethane |
| US6870024B2 (en) | 2002-09-09 | 2005-03-22 | Byk-Chemie Gmbh | Polymeric urea-urethane rheology control agents and a process for their preparation |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3701547A1 (en) * | 1987-01-21 | 1988-08-04 | Basf Lacke & Farben | POLYETHERURETHANE, METHOD FOR THE PRODUCTION THEREOF, LEVELING AGENTS AND USE OF POLYETHERURETHANE |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1316505A (en) * | 1960-10-12 | 1963-02-01 | Bayer Ag | Process for the manufacture of adducts from polyisocyanates and compounds containing reactive hydrogen combined with nitrogen |
| FR1360082A (en) * | 1962-06-07 | 1964-04-30 | Du Pont | Manufacture of linear segmental elastomers of the polyurethane type |
| GB1150818A (en) * | 1966-05-26 | 1969-05-07 | Allied Chem | Thermoplastic polyesterurethanes and coating compositions containing them |
-
0
- BE BE791999D patent/BE791999A/en unknown
-
1972
- 1972-10-02 CA CA153,060A patent/CA979566A/en not_active Expired
- 1972-11-06 IT IT3132672A patent/IT970240B/en active
- 1972-11-22 NL NL7215813A patent/NL7215813A/xx unknown
- 1972-11-23 DE DE19722257490 patent/DE2257490A1/en active Pending
- 1972-11-28 FR FR7242227A patent/FR2162015B1/fr not_active Expired
- 1972-11-28 JP JP47118598A patent/JPS4864123A/ja active Pending
- 1972-11-29 GB GB5521872A patent/GB1408165A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2139239A (en) * | 1983-05-03 | 1984-11-07 | Nl Industries Inc | Water soluble, modified polyurethane |
| US6870024B2 (en) | 2002-09-09 | 2005-03-22 | Byk-Chemie Gmbh | Polymeric urea-urethane rheology control agents and a process for their preparation |
| CN1305923C (en) * | 2002-09-09 | 2007-03-21 | 比克化学股份有限公司 | Polyurea-carbamate rheology control agent and its preparation method |
Also Published As
| Publication number | Publication date |
|---|---|
| IT970240B (en) | 1974-04-10 |
| CA979566A (en) | 1975-12-09 |
| DE2257490A1 (en) | 1973-06-07 |
| FR2162015A1 (en) | 1973-07-13 |
| BE791999A (en) | 1973-03-16 |
| FR2162015B1 (en) | 1977-01-14 |
| NL7215813A (en) | 1973-06-04 |
| JPS4864123A (en) | 1973-09-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1201962A (en) | Process for the production of a linear polyurethane | |
| GB1303201A (en) | ||
| ES8206577A1 (en) | Polyisocyanates for lacquers, process for their production and their use in thermosetting two-component polyurethane lacquers. | |
| GB1453157A (en) | Polyurethane adhesive composition with minimal moisture sensi tivity | |
| GB1257888A (en) | ||
| GB1432239A (en) | Polyurethane-polyurea materials | |
| GB1178698A (en) | Polyurethane Compositions | |
| GB1264950A (en) | ||
| GB1406511A (en) | Cellular polyurethanes | |
| GB1165830A (en) | Process for the preparation of Polyurethanes | |
| GB1197844A (en) | Process for the Production of Polyurethanes. | |
| GB1408165A (en) | Toluene diisocyanate urethane lacquer solutions | |
| GB1434070A (en) | Artificial leather sheet material and production thereof | |
| GB1460472A (en) | Polyureaurethane shock absorbing unit | |
| GB1491936A (en) | Cure of polyurethanes with mixed curatives | |
| GB1242780A (en) | Polyurethanes | |
| GB1458069A (en) | Polyurethanes | |
| GB1463069A (en) | Intumescent foams | |
| GB1261861A (en) | Stabilisation of organic isocyanates | |
| GB1127977A (en) | New polyurethane elastomers | |
| GB1266381A (en) | ||
| GB1513526A (en) | Dye dispersions | |
| GB1388748A (en) | Polyester-polyurethane polymers | |
| GB1313565A (en) | Polyurethanes | |
| GB1158270A (en) | Production of Elastomers Containing Urethane Groups. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |