DE3151854C2 - - Google Patents
Info
- Publication number
- DE3151854C2 DE3151854C2 DE3151854A DE3151854A DE3151854C2 DE 3151854 C2 DE3151854 C2 DE 3151854C2 DE 3151854 A DE3151854 A DE 3151854A DE 3151854 A DE3151854 A DE 3151854A DE 3151854 C2 DE3151854 C2 DE 3151854C2
- Authority
- DE
- Germany
- Prior art keywords
- hydroxyl
- coatings
- polyisocyanates
- hydroxyl groups
- formula
- 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 - Fee Related
Links
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 18
- 239000002904 solvent Substances 0.000 claims abstract description 10
- 239000011527 polyurethane coating Substances 0.000 claims abstract description 8
- 230000003647 oxidation Effects 0.000 claims abstract description 7
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 7
- 239000000049 pigment Substances 0.000 claims abstract description 6
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 4
- 239000002270 dispersing agent Substances 0.000 claims abstract description 3
- 239000000945 filler Substances 0.000 claims abstract description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract 2
- 239000008199 coating composition Substances 0.000 claims abstract 2
- 229930195733 hydrocarbon Natural products 0.000 claims abstract 2
- 239000005056 polyisocyanate Substances 0.000 claims description 17
- 229920001228 polyisocyanate Polymers 0.000 claims description 17
- 229920000058 polyacrylate Polymers 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 229920000620 organic polymer Polymers 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 6
- 239000012752 auxiliary agent Substances 0.000 abstract 1
- 229920005613 synthetic organic polymer Polymers 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 15
- 239000004814 polyurethane Substances 0.000 description 15
- 125000005442 diisocyanate group Chemical group 0.000 description 11
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 10
- 229920002635 polyurethane Polymers 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000004383 yellowing Methods 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
- 230000019612 pigmentation Effects 0.000 description 3
- 238000005829 trimerization reaction Methods 0.000 description 3
- AHBNSOZREBSAMG-UHFFFAOYSA-N 1,5-diisocyanato-2-methylpentane Chemical compound O=C=NCC(C)CCCN=C=O AHBNSOZREBSAMG-UHFFFAOYSA-N 0.000 description 2
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 2
- YOQVGIBXRRGAOX-UHFFFAOYSA-N 1-isocyanato-3-(isocyanatomethyl)pentane Chemical compound O=C=NCC(CC)CCN=C=O YOQVGIBXRRGAOX-UHFFFAOYSA-N 0.000 description 2
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- -1 isocyanato isocyanurate Chemical compound 0.000 description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- PDPUCIHVWBQCKT-UHFFFAOYSA-N 1,9-diisocyanato-2-methylnonane Chemical compound O=C=NCC(C)CCCCCCCN=C=O PDPUCIHVWBQCKT-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical group NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000005338 heat storage Methods 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
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)
- Insulated Conductors (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813151854 DE3151854A1 (de) | 1981-12-30 | 1981-12-30 | Thermisch- und oxidations-bestaendige polyurethanbeschichtungen |
| EP82111181A EP0083732B1 (de) | 1981-12-30 | 1982-12-02 | Thermisch und oxidationsbeständige Polyurethanbeschichtungen |
| AT82111181T ATE13435T1 (de) | 1981-12-30 | 1982-12-02 | Thermisch und oxidationsbestaendige polyurethanbeschichtungen. |
| DE8282111181T DE3263789D1 (en) | 1981-12-30 | 1982-12-02 | Heat and oxidation resistant polyurethane coatings |
| JP57227854A JPS58118862A (ja) | 1981-12-30 | 1982-12-28 | 耐熱性かつ耐酸化性のポリウレタンコーテイング剤 |
| US06/454,563 US4772665A (en) | 1981-12-30 | 1982-12-30 | Heat- and oxidation-resistant polyurethane coatings |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813151854 DE3151854A1 (de) | 1981-12-30 | 1981-12-30 | Thermisch- und oxidations-bestaendige polyurethanbeschichtungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE3151854A1 DE3151854A1 (de) | 1983-07-07 |
| DE3151854C2 true DE3151854C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1992-06-17 |
Family
ID=6149976
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19813151854 Granted DE3151854A1 (de) | 1981-12-30 | 1981-12-30 | Thermisch- und oxidations-bestaendige polyurethanbeschichtungen |
| DE8282111181T Expired DE3263789D1 (en) | 1981-12-30 | 1982-12-02 | Heat and oxidation resistant polyurethane coatings |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE8282111181T Expired DE3263789D1 (en) | 1981-12-30 | 1982-12-02 | Heat and oxidation resistant polyurethane coatings |
Country Status (5)
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3322718A1 (de) * | 1983-06-24 | 1985-01-03 | Chemische Werke Hüls AG, 4370 Marl | Als pulverlack bzw. bindemittel fuer pulverlacke geeignetes stoffgemisch |
| DE19752691A1 (de) * | 1997-11-28 | 1999-06-02 | Huels Chemische Werke Ag | 2K-PUR-Beschichtungszusammensetzung |
| DE19804451A1 (de) * | 1998-02-05 | 1999-09-02 | Degussa | Wäßrige Zweikomponenten- Polyurethanbeschichtungszusammensetzungen auf Basis von 2-Methylpentan-1,5-diisocyanat |
| RU2215012C2 (ru) * | 2001-11-27 | 2003-10-27 | Федеральное государственное унитарное предприятие "Всероссийский научно-исследовательский институт авиационных материалов" | Состав для защиты полимерных композиционных материалов |
| US7072115B2 (en) * | 2002-03-26 | 2006-07-04 | Keiwa Inc. | Light diffusion sheet and backlight unit using the same |
| US11932747B2 (en) | 2020-06-24 | 2024-03-19 | Evonik Operations Gmbh | Use of long-chain citric acid esters in aqueous polyurethane dispersions |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA755152A (en) * | 1967-03-21 | Kerrigan Vincent | Polyurethane coating compositions | |
| US3115479A (en) * | 1955-12-08 | 1963-12-24 | R oconr | |
| GB837120A (en) * | 1957-06-12 | 1960-06-09 | Ici Ltd | Trimerisation of organic isocyanates |
| FR1343812A (fr) * | 1961-10-26 | 1963-11-22 | Ici Ltd | Enduits superficiels en polyuréthane et leur fabrication |
| NL290668A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1962-03-27 | |||
| US3631198A (en) * | 1966-09-07 | 1971-12-28 | Nat Distillers Chem Corp | Preparation of 1 5-diisocyanato-2-methylpentane |
| DE2806731A1 (de) * | 1978-02-17 | 1979-08-23 | Bayer Ag | Verfahren zur herstellung von isocyanuratgruppen aufweisenden polyisocyanaten |
| DE2938855A1 (de) * | 1979-09-26 | 1981-04-09 | Chemische Werke Hüls AG, 4370 Marl | Einkomponenten-einbrennlacke |
| DE3100263A1 (de) * | 1981-01-08 | 1982-08-12 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von isocyanuratgruppen aufweisenden polyisocyanaten und ihre verwendung bei der herstellung von polyurethanen |
-
1981
- 1981-12-30 DE DE19813151854 patent/DE3151854A1/de active Granted
-
1982
- 1982-12-02 EP EP82111181A patent/EP0083732B1/de not_active Expired
- 1982-12-02 AT AT82111181T patent/ATE13435T1/de not_active IP Right Cessation
- 1982-12-02 DE DE8282111181T patent/DE3263789D1/de not_active Expired
- 1982-12-28 JP JP57227854A patent/JPS58118862A/ja active Granted
- 1982-12-30 US US06/454,563 patent/US4772665A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH029065B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1990-02-28 |
| EP0083732A1 (de) | 1983-07-20 |
| DE3151854A1 (de) | 1983-07-07 |
| EP0083732B1 (de) | 1985-05-22 |
| ATE13435T1 (de) | 1985-06-15 |
| US4772665A (en) | 1988-09-20 |
| JPS58118862A (ja) | 1983-07-15 |
| DE3263789D1 (en) | 1985-06-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8127 | New person/name/address of the applicant |
Owner name: HUELS AG, 4370 MARL, DE |
|
| 8110 | Request for examination paragraph 44 | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |