SK15662002A3 - Zmesi izokyanátov blokovaných dimetylpyrazolom - Google Patents
Zmesi izokyanátov blokovaných dimetylpyrazolom Download PDFInfo
- Publication number
- SK15662002A3 SK15662002A3 SK1566-2002A SK15662002A SK15662002A3 SK 15662002 A3 SK15662002 A3 SK 15662002A3 SK 15662002 A SK15662002 A SK 15662002A SK 15662002 A3 SK15662002 A3 SK 15662002A3
- Authority
- SK
- Slovakia
- Prior art keywords
- blocked
- lacquer
- polyisocyanate
- polyisocyanates
- solution
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 44
- 239000012948 isocyanate Substances 0.000 title description 4
- 150000002513 isocyanates Chemical class 0.000 title description 4
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 76
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 76
- SDXAWLJRERMRKF-UHFFFAOYSA-N 3,5-dimethyl-1h-pyrazole Chemical compound CC=1C=C(C)NN=1 SDXAWLJRERMRKF-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000004922 lacquer Substances 0.000 claims description 49
- 229920000877 Melamine resin Polymers 0.000 claims description 16
- 239000002966 varnish Substances 0.000 claims description 14
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 13
- 239000002981 blocking agent Substances 0.000 claims description 7
- 125000005442 diisocyanate group Chemical group 0.000 claims description 4
- 210000003298 dental enamel Anatomy 0.000 abstract description 4
- 238000000576 coating method Methods 0.000 abstract description 3
- 239000003431 cross linking reagent Substances 0.000 abstract 1
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 description 24
- 239000011230 binding agent Substances 0.000 description 21
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 15
- 239000007787 solid Substances 0.000 description 15
- 239000002253 acid Substances 0.000 description 13
- 239000004640 Melamine resin Substances 0.000 description 12
- 238000005562 fading Methods 0.000 description 10
- 238000002156 mixing Methods 0.000 description 10
- 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 9
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- ZAXXZBQODQDCOW-UHFFFAOYSA-N 1-methoxypropyl acetate Chemical compound CCC(OC)OC(C)=O ZAXXZBQODQDCOW-UHFFFAOYSA-N 0.000 description 7
- 239000005058 Isophorone diisocyanate Substances 0.000 description 7
- 238000004132 cross linking Methods 0.000 description 7
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000008096 xylene Substances 0.000 description 6
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 229920000058 polyacrylate Polymers 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- 239000004971 Cross linker Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- RSOILICUEWXSLA-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1 RSOILICUEWXSLA-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- UJRDRFZCRQNLJM-UHFFFAOYSA-N methyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OC)=CC(N2N=C3C=CC=CC3=N2)=C1O UJRDRFZCRQNLJM-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000005829 trimerization reaction Methods 0.000 description 2
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
- WHIVNJATOVLWBW-PLNGDYQASA-N (nz)-n-butan-2-ylidenehydroxylamine Chemical compound CC\C(C)=N/O WHIVNJATOVLWBW-PLNGDYQASA-N 0.000 description 1
- ROHUXHMNZLHBSF-UHFFFAOYSA-N 1,4-bis(isocyanatomethyl)cyclohexane Chemical compound O=C=NCC1CCC(CN=C=O)CC1 ROHUXHMNZLHBSF-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
- PJMDLNIAGSYXLA-UHFFFAOYSA-N 6-iminooxadiazine-4,5-dione Chemical compound N=C1ON=NC(=O)C1=O PJMDLNIAGSYXLA-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 102000020897 Formins Human genes 0.000 description 1
- 108091022623 Formins Proteins 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000002320 enamel (paints) Substances 0.000 description 1
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N p-toluenesulfonic acid Substances CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000004924 water-based lacquer 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
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10022036A DE10022036A1 (de) | 2000-05-05 | 2000-05-05 | Dimethylpyrazol-blockierte Isocyanatgemische |
| PCT/EP2001/004546 WO2001085823A1 (de) | 2000-05-05 | 2001-04-23 | Dimethylpyrazol-blockierte isocyanatgemische |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK15662002A3 true SK15662002A3 (sk) | 2003-04-01 |
Family
ID=7640966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK1566-2002A SK15662002A3 (sk) | 2000-05-05 | 2001-04-23 | Zmesi izokyanátov blokovaných dimetylpyrazolom |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US6713556B2 (ru) |
| EP (1) | EP1285014B1 (ru) |
| JP (1) | JP2003532769A (ru) |
| CN (1) | CN1164638C (ru) |
| AT (1) | ATE261463T1 (ru) |
| AU (2) | AU2001273960B2 (ru) |
| BR (1) | BR0110444A (ru) |
| CA (1) | CA2407805C (ru) |
| CZ (1) | CZ20023650A3 (ru) |
| DE (2) | DE10022036A1 (ru) |
| ES (1) | ES2215904T3 (ru) |
| HK (1) | HK1056887A1 (ru) |
| HU (1) | HUP0301929A3 (ru) |
| MX (1) | MXPA02010838A (ru) |
| PL (1) | PL358294A1 (ru) |
| PT (1) | PT1285014E (ru) |
| RU (1) | RU2292359C2 (ru) |
| SK (1) | SK15662002A3 (ru) |
| WO (1) | WO2001085823A1 (ru) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003074617A1 (de) * | 2002-03-02 | 2003-09-12 | Basf Coatings Ag | Von unlöslichen festkörpern freie elektrotauchlacke |
| DE10322432A1 (de) * | 2003-05-19 | 2004-12-16 | Basf Coatings Ag | Thermisch härtbare Einkomponenten-Beschichtungsstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung |
| JP5574603B2 (ja) * | 2006-01-13 | 2014-08-20 | ビーエーエスエフ ソシエタス・ヨーロピア | イソシアネート含有調製物 |
| JP6484268B2 (ja) * | 2017-03-09 | 2019-03-13 | 三洋化成工業株式会社 | ブロックイソシアネートの製造方法 |
| WO2019057448A1 (de) | 2017-09-25 | 2019-03-28 | Basf Se | Zumindest teilweise blockiertes polyisocyanat (bp) |
| CN109627422B (zh) * | 2018-11-19 | 2021-04-20 | 万华化学集团股份有限公司 | 一种丁酮肟封闭多异氰酸酯的制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8405320D0 (en) * | 1984-02-29 | 1984-04-04 | Baxenden Chem | Blocked isocyanates |
| DE4441418A1 (de) | 1994-11-22 | 1996-05-23 | Bayer Ag | Verfahren zur Herstellung von 3,5-Dimethylpyrazol-blockierten Polyisocyanaten |
| US6025433A (en) * | 1995-12-20 | 2000-02-15 | Basf Coatings Ag | Thermosetting paint composition |
-
2000
- 2000-05-05 DE DE10022036A patent/DE10022036A1/de not_active Withdrawn
-
2001
- 2001-04-23 DE DE50101663T patent/DE50101663D1/de not_active Expired - Lifetime
- 2001-04-23 BR BR0110444-6A patent/BR0110444A/pt not_active IP Right Cessation
- 2001-04-23 CZ CZ20023650A patent/CZ20023650A3/cs unknown
- 2001-04-23 CN CNB018090044A patent/CN1164638C/zh not_active Expired - Lifetime
- 2001-04-23 RU RU2002132901/04A patent/RU2292359C2/ru not_active IP Right Cessation
- 2001-04-23 ES ES01940353T patent/ES2215904T3/es not_active Expired - Lifetime
- 2001-04-23 PT PT01940353T patent/PT1285014E/pt unknown
- 2001-04-23 CA CA002407805A patent/CA2407805C/en not_active Expired - Fee Related
- 2001-04-23 AU AU2001273960A patent/AU2001273960B2/en not_active Ceased
- 2001-04-23 MX MXPA02010838A patent/MXPA02010838A/es active IP Right Grant
- 2001-04-23 AU AU7396001A patent/AU7396001A/xx active Pending
- 2001-04-23 PL PL01358294A patent/PL358294A1/xx unknown
- 2001-04-23 EP EP01940353A patent/EP1285014B1/de not_active Expired - Lifetime
- 2001-04-23 HU HU0301929A patent/HUP0301929A3/hu unknown
- 2001-04-23 US US10/275,088 patent/US6713556B2/en not_active Expired - Lifetime
- 2001-04-23 SK SK1566-2002A patent/SK15662002A3/sk unknown
- 2001-04-23 AT AT01940353T patent/ATE261463T1/de not_active IP Right Cessation
- 2001-04-23 JP JP2001582418A patent/JP2003532769A/ja active Pending
- 2001-04-23 WO PCT/EP2001/004546 patent/WO2001085823A1/de not_active Application Discontinuation
-
2003
- 2003-12-22 HK HK03109298A patent/HK1056887A1/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1285014A1 (de) | 2003-02-26 |
| ES2215904T3 (es) | 2004-10-16 |
| DE50101663D1 (de) | 2004-04-15 |
| HK1056887A1 (en) | 2004-03-05 |
| CA2407805A1 (en) | 2002-10-30 |
| CN1164638C (zh) | 2004-09-01 |
| AU7396001A (en) | 2001-11-20 |
| BR0110444A (pt) | 2003-04-08 |
| HUP0301929A2 (hu) | 2003-09-29 |
| WO2001085823A1 (de) | 2001-11-15 |
| MXPA02010838A (es) | 2003-05-27 |
| US6713556B2 (en) | 2004-03-30 |
| CZ20023650A3 (cs) | 2003-02-12 |
| JP2003532769A (ja) | 2003-11-05 |
| PT1285014E (pt) | 2004-06-30 |
| US20030171488A1 (en) | 2003-09-11 |
| RU2292359C2 (ru) | 2007-01-27 |
| DE10022036A1 (de) | 2001-11-08 |
| CN1427859A (zh) | 2003-07-02 |
| EP1285014B1 (de) | 2004-03-10 |
| ATE261463T1 (de) | 2004-03-15 |
| CA2407805C (en) | 2009-03-24 |
| HUP0301929A3 (en) | 2007-09-28 |
| PL358294A1 (en) | 2004-08-09 |
| AU2001273960B2 (en) | 2004-08-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB9A | Suspension of patent application procedure |