JPS6013858A - イソシアネ−ト樹脂を基礎とする吸湿硬化性塗料 - Google Patents
イソシアネ−ト樹脂を基礎とする吸湿硬化性塗料Info
- Publication number
- JPS6013858A JPS6013858A JP59127656A JP12765684A JPS6013858A JP S6013858 A JPS6013858 A JP S6013858A JP 59127656 A JP59127656 A JP 59127656A JP 12765684 A JP12765684 A JP 12765684A JP S6013858 A JPS6013858 A JP S6013858A
- Authority
- JP
- Japan
- Prior art keywords
- moisture
- resin
- weight
- diisocyanate
- mixture
- 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.)
- Granted
Links
- 239000011347 resin Substances 0.000 title claims abstract description 39
- 229920005989 resin Polymers 0.000 title claims abstract description 39
- 239000003973 paint Substances 0.000 title claims description 6
- 239000012948 isocyanate Substances 0.000 title abstract description 7
- 150000002513 isocyanates Chemical class 0.000 title abstract description 4
- 239000000203 mixture Substances 0.000 claims abstract description 25
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 238000013008 moisture curing Methods 0.000 claims description 7
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 7
- 239000001294 propane Substances 0.000 claims description 4
- 239000001273 butane Substances 0.000 claims description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000002904 solvent Substances 0.000 abstract description 13
- 239000000049 pigment Substances 0.000 abstract description 6
- 230000001590 oxidative effect Effects 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 3
- 239000002966 varnish Substances 0.000 abstract 2
- AHBNSOZREBSAMG-UHFFFAOYSA-N 1,5-diisocyanato-2-methylpentane Chemical compound O=C=NCC(C)CCCN=C=O AHBNSOZREBSAMG-UHFFFAOYSA-N 0.000 abstract 1
- YOQVGIBXRRGAOX-UHFFFAOYSA-N 1-isocyanato-3-(isocyanatomethyl)pentane Chemical compound O=C=NCC(CC)CCN=C=O YOQVGIBXRRGAOX-UHFFFAOYSA-N 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 18
- 239000011248 coating agent Substances 0.000 description 9
- 238000001723 curing Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 210000003127 knee Anatomy 0.000 description 5
- 229920001228 polyisocyanate Polymers 0.000 description 5
- 239000005056 polyisocyanate Substances 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- -1 aliphatic isocyanate Chemical class 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 238000006471 dimerization reaction Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- 239000004914 cyclooctane Substances 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- 239000012463 white pigment 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
- C08G18/80—Masked polyisocyanates
- C08G18/8003—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen
- C08G18/8006—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32
- C08G18/8009—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203
- C08G18/8022—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203 with polyols having at least three hydroxy groups
- C08G18/8025—Masked aliphatic or cycloaliphatic polyisocyanates
-
- 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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4266—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones
- C08G18/4269—Lactones
- C08G18/4277—Caprolactone and/or substituted caprolactone
-
- 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
- C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
-
- 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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19833322723 DE3322723A1 (de) | 1983-06-24 | 1983-06-24 | Feuchtigkeitshaertende lacke auf isocyanatharz-basis |
| DE3322723.3 | 1983-06-24 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6013858A true JPS6013858A (ja) | 1985-01-24 |
| JPH0377232B2 JPH0377232B2 (enExample) | 1991-12-09 |
Family
ID=6202246
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59127656A Granted JPS6013858A (ja) | 1983-06-24 | 1984-06-22 | イソシアネ−ト樹脂を基礎とする吸湿硬化性塗料 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4518740A (enExample) |
| EP (1) | EP0132514B1 (enExample) |
| JP (1) | JPS6013858A (enExample) |
| AT (1) | ATE28204T1 (enExample) |
| DE (2) | DE3322723A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014058684A (ja) * | 1998-04-22 | 2014-04-03 | 3M Co | 可撓性ポリウレタン材料 |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3621706A1 (de) * | 1986-06-28 | 1988-01-07 | Bayer Ag | Verfahren zur herstellung von isocyanatgruppen aufweisenden prepolymeren, die nach diesem verfahren erhaeltlichen prepolymeren und ihre verwendung als bindemittel in einkomponentenlacken |
| US4892920A (en) * | 1988-11-21 | 1990-01-09 | Air Products And Chemicals, Inc. | Process for the preparation of cyclohexanediisocyanate containing polyisocyanate prepolymers and polyurethanes having high temperature performance |
| DE19752691A1 (de) * | 1997-11-28 | 1999-06-02 | Huels Chemische Werke Ag | 2K-PUR-Beschichtungszusammensetzung |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3284413A (en) * | 1964-12-16 | 1966-11-08 | Mobay Chemical Corp | Prepolymer isocyanurate resins |
| US3631198A (en) * | 1966-09-07 | 1971-12-28 | Nat Distillers Chem Corp | Preparation of 1 5-diisocyanato-2-methylpentane |
| DE1795417A1 (de) * | 1968-09-27 | 1972-01-05 | Bayer Ag | Verfahren zur Herstellung physiologisch unbedenklicher,aliphatischer Polyisocyanate |
| US4234445A (en) * | 1979-01-25 | 1980-11-18 | Uniroyal, Inc. | Polyurethane spray composition containing lactone viscosity modifier |
| DE2845514A1 (de) * | 1978-10-19 | 1980-04-30 | Bayer Ag | Isocyanatgemisch und seine verwendung als bindemittel in einkomponenten-lacken |
-
1983
- 1983-06-24 DE DE19833322723 patent/DE3322723A1/de not_active Withdrawn
-
1984
- 1984-04-26 AT AT84104673T patent/ATE28204T1/de not_active IP Right Cessation
- 1984-04-26 EP EP84104673A patent/EP0132514B1/de not_active Expired
- 1984-04-26 DE DE8484104673T patent/DE3464615D1/de not_active Expired
- 1984-05-14 US US06/609,643 patent/US4518740A/en not_active Expired - Fee Related
- 1984-06-22 JP JP59127656A patent/JPS6013858A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014058684A (ja) * | 1998-04-22 | 2014-04-03 | 3M Co | 可撓性ポリウレタン材料 |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE28204T1 (de) | 1987-07-15 |
| JPH0377232B2 (enExample) | 1991-12-09 |
| DE3322723A1 (de) | 1985-01-03 |
| US4518740A (en) | 1985-05-21 |
| EP0132514A1 (de) | 1985-02-13 |
| EP0132514B1 (de) | 1987-07-08 |
| DE3464615D1 (en) | 1987-08-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1651704B1 (en) | Coating compositions containing aminofunctional silicone resins | |
| US3770703A (en) | Heat hardenable mixtures of epsilon-caprolactam blocked polyisocyanates and cycloaliphatic polyamines | |
| CA1187083A (en) | Blocked polyisocyanate compounds and polyurethane heat-curing coatings containing said compounds | |
| DE1694237A1 (de) | Verfahren zur Herstellung von vernetzten Kunststoffen und Flaechengebilden | |
| US4375539A (en) | Solid blocked crosslinking agents based on 1,4-cyclohexane bis(methylisocyanate) | |
| US4388245A (en) | Process for preparing organic polyisocyanate compositions | |
| JPS6013858A (ja) | イソシアネ−ト樹脂を基礎とする吸湿硬化性塗料 | |
| US3632845A (en) | Soluble cured polyester polyurethanes | |
| US4124569A (en) | Process for the preparation of polyisocyanates containing urethane and biuret groups | |
| US4952632A (en) | Trans-cyclohexane-1,4-diisocyanate which is completely or partially blocked with epsilon-caprolactam; and the manufacture and use of the same | |
| US6077960A (en) | Uretedione derivative, curable resin composition comprising the same, and process for producing the same | |
| JPH09249731A (ja) | ブロックされた脂肪族ジイソシアネートまたは−ジイソシアネート付加物 | |
| US5034495A (en) | Novel hardening agents | |
| JPH0776670A (ja) | Ｐｕｒエラストマーを製造するための二成分系被覆材料 | |
| US5545705A (en) | Aldimines based on 2-methyl-1,5-pentane diamine and their use for the production of polyurea coatings | |
| CA2169226A1 (en) | Blocked polyisocyanates, process for their preparation, and coating materials and coating systems produced therefrom | |
| JPS58118862A (ja) | 耐熱性かつ耐酸化性のポリウレタンコーテイング剤 | |
| JPH04234470A (ja) | 室温で硬化する光安定性の反応性二成分系ポリウレタン塗料 | |
| EP1106613B1 (en) | Uretedione derivative, curable resin composition comprising the same, and process for producing the same | |
| CN115873203B (zh) | 高耐磨单组分水性聚氨酯及其乳液或分散体、涂层的制备方法及应用 | |
| JP2000159862A (ja) | １成分熱硬化性塗料組成物 | |
| JPS5995259A (ja) | 有機ポリイソシアネ−ト及びその製造方法 | |
| EP0417824A1 (en) | Resin composition comprising a polyurethane/urea containing primary amine or blocked primary amine functions and a cross-linking agent | |
| JPH10139850A (ja) | 塗料用ポリイソシアネート、その製造方法、その使用、２ｋ−ｐｕｒ−塗料及び湿気硬化形１ｋ−ｐｕｒ−塗料 | |
| US4803245A (en) | Flexibilized phenol/mercapto resins and their synthesis |