CH625256A5 - - Google Patents
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- Publication number
- CH625256A5 CH625256A5 CH463776A CH463776A CH625256A5 CH 625256 A5 CH625256 A5 CH 625256A5 CH 463776 A CH463776 A CH 463776A CH 463776 A CH463776 A CH 463776A CH 625256 A5 CH625256 A5 CH 625256A5
- Authority
- CH
- Switzerland
- Prior art keywords
- reaction
- prepolymer
- mixture
- tetrabromoethane
- dabco
- Prior art date
Links
- 238000006243 chemical reaction Methods 0.000 description 22
- 239000003054 catalyst Substances 0.000 description 16
- RVHSTXJKKZWWDQ-UHFFFAOYSA-N 1,1,1,2-tetrabromoethane Chemical compound BrCC(Br)(Br)Br RVHSTXJKKZWWDQ-UHFFFAOYSA-N 0.000 description 13
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 13
- 238000000034 method Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- FTTATHOUSOIFOQ-UHFFFAOYSA-N 1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrazine Chemical compound C1NCCN2CCCC21 FTTATHOUSOIFOQ-UHFFFAOYSA-N 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 6
- 230000003197 catalytic effect Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 229920001228 polyisocyanate Polymers 0.000 description 4
- 239000005056 polyisocyanate Substances 0.000 description 4
- 229920005903 polyol mixture Polymers 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 4
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical class CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000013256 coordination polymer Substances 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ATWLRNODAYAMQS-UHFFFAOYSA-N 1,1-dibromopropane Chemical compound CCC(Br)Br ATWLRNODAYAMQS-UHFFFAOYSA-N 0.000 description 1
- HEBTZZBBPUFAFE-UHFFFAOYSA-N 2-methyl-n-(oxomethylidene)benzenesulfonamide Chemical compound CC1=CC=CC=C1S(=O)(=O)N=C=O HEBTZZBBPUFAFE-UHFFFAOYSA-N 0.000 description 1
- VLJQDHDVZJXNQL-UHFFFAOYSA-N 4-methyl-n-(oxomethylidene)benzenesulfonamide Chemical compound CC1=CC=C(S(=O)(=O)N=C=O)C=C1 VLJQDHDVZJXNQL-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- -1 chlorides p-nitrobenzoyl chloride Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 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
- C08G18/08—Processes
- C08G18/16—Catalysts
-
- 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
- C08G18/089—Reaction retarding agents
-
- 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
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/20—Heterocyclic amines; Salts thereof
- C08G18/2045—Heterocyclic amines; Salts thereof containing condensed heterocyclic rings
- C08G18/2063—Heterocyclic amines; Salts thereof containing condensed heterocyclic rings having two nitrogen atoms in the condensed ring system
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT284675A AT337991B (de) | 1975-04-15 | 1975-04-15 | Verfahren zur katalysierten herstellung von polyurethanprapolymeren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH625256A5 true CH625256A5 (en, 2012) | 1981-09-15 |
Family
ID=3541219
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH463776A CH625256A5 (en, 2012) | 1975-04-15 | 1976-04-12 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4026875A (en, 2012) |
| JP (1) | JPS5940847B2 (en, 2012) |
| AT (1) | AT337991B (en, 2012) |
| BR (1) | BR7602259A (en, 2012) |
| CH (1) | CH625256A5 (en, 2012) |
| DE (1) | DE2612649A1 (en, 2012) |
| FR (1) | FR2307831A1 (en, 2012) |
| MX (1) | MX3616E (en, 2012) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006005938A1 (de) * | 2006-02-09 | 2007-08-16 | Fachhochschule Münster | Emissionsarme Polyurethane |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4839456A (en) * | 1983-07-12 | 1989-06-13 | Keith Kent | Self-adhesive, drag reducing polymeric coating |
| US4574793A (en) * | 1984-08-21 | 1986-03-11 | Hexcel Corporation | Stabilized, catalyzed water activated polyurethane systems |
| US5648412A (en) * | 1995-01-30 | 1997-07-15 | The Dow Chemical Company | Blow-moldable rigid thermoplastic polyurethane resins |
| DE10348555A1 (de) * | 2003-10-20 | 2005-05-19 | Henkel Kgaa | Lagerstabiles, Silylgruppen tragendes Polyurethan |
| DE10351530A1 (de) * | 2003-11-03 | 2005-06-16 | Basf Ag | Verfahren zur Herstellung von Isocyanatgruppen enthaltenden Prepolymeren |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2692873A (en) * | 1951-07-19 | 1954-10-26 | Du Pont | Elastomers from polyalkylene ether glycol reacted with arylene diisocyanate and water |
| US2817643A (en) * | 1955-09-15 | 1957-12-24 | Farben Fabriken Bayer Ag | Mixed polyurethane lacquer and method of coating therewith |
| GB996767A (en) * | 1962-08-28 | 1965-06-30 | Polycell Prod Ltd | Polyurethane compositions |
| DE1245590B (de) * | 1965-12-30 | 1967-07-27 | Bayer Ag | Monoisocyanate als wasserbindende Mittel fuer Polyurethanmassen |
| GB1175961A (en) * | 1966-01-27 | 1970-01-01 | Ici Ltd | Stabilised Compositions useful in the Manufacture of Polyurethane Foams |
| BE758355A (fr) * | 1969-11-03 | 1971-04-16 | Goodrich Co B F | Solutions de polyurethane stables a la chaleur |
-
1975
- 1975-04-15 AT AT284675A patent/AT337991B/de not_active IP Right Cessation
-
1976
- 1976-03-25 DE DE19762612649 patent/DE2612649A1/de active Granted
- 1976-04-07 US US05/674,408 patent/US4026875A/en not_active Expired - Lifetime
- 1976-04-07 MX MX764225U patent/MX3616E/es unknown
- 1976-04-12 CH CH463776A patent/CH625256A5/de not_active IP Right Cessation
- 1976-04-13 FR FR7610807A patent/FR2307831A1/fr active Granted
- 1976-04-13 BR BR7602259A patent/BR7602259A/pt unknown
- 1976-04-15 JP JP51041948A patent/JPS5940847B2/ja not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006005938A1 (de) * | 2006-02-09 | 2007-08-16 | Fachhochschule Münster | Emissionsarme Polyurethane |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2612649A1 (de) | 1976-10-28 |
| FR2307831A1 (fr) | 1976-11-12 |
| US4026875A (en) | 1977-05-31 |
| JPS5940847B2 (ja) | 1984-10-03 |
| JPS51127199A (en) | 1976-11-05 |
| AT337991B (de) | 1977-07-25 |
| FR2307831B1 (en, 2012) | 1980-04-30 |
| BR7602259A (pt) | 1976-10-12 |
| DE2612649C2 (en, 2012) | 1989-04-13 |
| MX3616E (es) | 1981-04-01 |
| ATA284675A (de) | 1976-11-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |