CA2119882A1 - Mousse expansee sans utilisation de cfc - Google Patents
Mousse expansee sans utilisation de cfcInfo
- Publication number
- CA2119882A1 CA2119882A1 CA002119882A CA2119882A CA2119882A1 CA 2119882 A1 CA2119882 A1 CA 2119882A1 CA 002119882 A CA002119882 A CA 002119882A CA 2119882 A CA2119882 A CA 2119882A CA 2119882 A1 CA2119882 A1 CA 2119882A1
- Authority
- CA
- Canada
- Prior art keywords
- composition
- present
- weight
- range
- phosphate
- 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.)
- Abandoned
Links
- 239000006260 foam Substances 0.000 title claims abstract description 52
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 18
- 239000000203 mixture Substances 0.000 claims abstract description 100
- 229920005862 polyol Polymers 0.000 claims description 33
- 150000003077 polyols Chemical class 0.000 claims description 33
- 239000003054 catalyst Substances 0.000 claims description 31
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 23
- 229920005906 polyester polyol Polymers 0.000 claims description 23
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 21
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 18
- 229920000570 polyether Polymers 0.000 claims description 18
- 150000001412 amines Chemical class 0.000 claims description 15
- 239000012948 isocyanate Substances 0.000 claims description 13
- 150000002513 isocyanates Chemical class 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 10
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 10
- 239000004094 surface-active agent Substances 0.000 claims description 10
- 239000003063 flame retardant Substances 0.000 claims description 9
- ACRQLFSHISNWRY-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-phenoxybenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=CC=CC=C1 ACRQLFSHISNWRY-UHFFFAOYSA-N 0.000 claims description 8
- 229920001228 polyisocyanate Polymers 0.000 claims description 8
- 239000005056 polyisocyanate Substances 0.000 claims description 8
- -1 molybedenum trioxide Chemical compound 0.000 claims description 7
- 239000004254 Ammonium phosphate Substances 0.000 claims description 6
- 229910000148 ammonium phosphate Inorganic materials 0.000 claims description 6
- 235000019289 ammonium phosphates Nutrition 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 6
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 6
- 239000011495 polyisocyanurate Substances 0.000 claims description 6
- 229920000582 polyisocyanurate Polymers 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 229920000877 Melamine resin Polymers 0.000 claims description 4
- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical compound NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 claims description 4
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 claims description 4
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 4
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 4
- 150000008282 halocarbons Chemical class 0.000 claims description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 4
- HQUQLFOMPYWACS-UHFFFAOYSA-N tris(2-chloroethyl) phosphate Chemical compound ClCCOP(=O)(OCCCl)OCCCl HQUQLFOMPYWACS-UHFFFAOYSA-N 0.000 claims description 4
- XRJYCRCXOMYXPA-UHFFFAOYSA-N P(O)(O)=O.ClCCC(=C(CCCl)CCCl)CCCl Chemical compound P(O)(O)=O.ClCCC(=C(CCCl)CCCl)CCCl XRJYCRCXOMYXPA-UHFFFAOYSA-N 0.000 claims description 3
- PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical compound BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 claims description 3
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- GTRSAMFYSUBAGN-UHFFFAOYSA-N tris(2-chloropropyl) phosphate Chemical compound CC(Cl)COP(=O)(OCC(C)Cl)OCC(C)Cl GTRSAMFYSUBAGN-UHFFFAOYSA-N 0.000 claims description 3
- BOWAERGBTFJCGG-UHFFFAOYSA-N 1,1-dibromo-2-(2,2-dibromoethyl)cyclohexane Chemical compound BrC(Br)CC1CCCCC1(Br)Br BOWAERGBTFJCGG-UHFFFAOYSA-N 0.000 claims 2
- DEIGXXQKDWULML-UHFFFAOYSA-N 1,2,5,6,9,10-hexabromocyclododecane Chemical compound BrC1CCC(Br)C(Br)CCC(Br)C(Br)CCC1Br DEIGXXQKDWULML-UHFFFAOYSA-N 0.000 claims 2
- QWVCIORZLNBIIC-UHFFFAOYSA-N 2,3-dibromopropan-1-ol Chemical compound OCC(Br)CBr QWVCIORZLNBIIC-UHFFFAOYSA-N 0.000 claims 2
- DHNUXDYAOVSGII-UHFFFAOYSA-N tris(1,3-dichloropropyl) phosphate Chemical compound ClCCC(Cl)OP(=O)(OC(Cl)CCCl)OC(Cl)CCCl DHNUXDYAOVSGII-UHFFFAOYSA-N 0.000 claims 2
- NKLPNHRUMYAQJV-UHFFFAOYSA-N 1,6-dichloro-3,4-bis(2-chloroethyl)hex-3-ene Chemical group ClCCC(CCCl)=C(CCCl)CCCl NKLPNHRUMYAQJV-UHFFFAOYSA-N 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract description 8
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 3
- 239000007921 spray Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 6
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 5
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 5
- 235000019837 monoammonium phosphate Nutrition 0.000 description 5
- 239000006012 monoammonium phosphate Substances 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 150000002009 diols Chemical class 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical class OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 3
- QKUNKVYPGIOQNP-UHFFFAOYSA-N 4,8,11,14,17,21-hexachlorotetracosane Chemical compound CCCC(Cl)CCCC(Cl)CCC(Cl)CCC(Cl)CCC(Cl)CCCC(Cl)CCC QKUNKVYPGIOQNP-UHFFFAOYSA-N 0.000 description 2
- FCLYQYOJLQDQNA-BNWDXEGFSA-N 4-Deacetylneosolaniol Chemical compound C([C@@]12[C@]3(C)[C@H](O)[C@@H](O)[C@H]1O[C@@H]1C=C(C)[C@@H](O)C[C@@]13COC(=O)C)O2 FCLYQYOJLQDQNA-BNWDXEGFSA-N 0.000 description 2
- 239000004114 Ammonium polyphosphate Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 2
- 229920001276 ammonium polyphosphate Polymers 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 2
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical group C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate Chemical compound [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000004620 low density foam Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229920005896 rigid polyol Polymers 0.000 description 1
- 239000011493 spray foam Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 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 description 1
- 238000005829 trimerization reaction Methods 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 239000004034 viscosity adjusting agent 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/1875—Catalysts containing secondary or tertiary amines or salts thereof containing ammonium salts or mixtures of secondary of tertiary amines and acids
-
- 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
- C08G18/2009—Heterocyclic amines; Salts thereof containing one heterocyclic ring
- C08G18/2036—Heterocyclic amines; Salts thereof containing one heterocyclic ring having at least three nitrogen atoms in the ring
-
- 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
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4018—Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
-
- 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
- C08G18/48—Polyethers
- C08G18/4804—Two or more polyethers of different physical or chemical nature
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0083—Foam properties prepared using water as the sole blowing agent
-
- 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
- C08G2115/00—Oligomerisation
- C08G2115/02—Oligomerisation to isocyanurate groups
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)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Insulated Conductors (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67509591A | 1991-03-25 | 1991-03-25 | |
| US675,095 | 1991-03-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2119882A1 true CA2119882A1 (fr) | 1992-10-01 |
Family
ID=24709034
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002119882A Abandoned CA2119882A1 (fr) | 1991-03-25 | 1991-04-19 | Mousse expansee sans utilisation de cfc |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0615526A4 (fr) |
| AU (1) | AU7858991A (fr) |
| BR (1) | BR9107331A (fr) |
| CA (1) | CA2119882A1 (fr) |
| HU (1) | HUT68199A (fr) |
| MY (1) | MY106388A (fr) |
| WO (1) | WO1992016574A1 (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5169872A (en) * | 1992-05-11 | 1992-12-08 | Dow Corning Corporation | Process for preparing rigid polyurethane and polyisocyanurate foams having enhanced benefits |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3943075A (en) * | 1970-06-19 | 1976-03-09 | Dunlop Holdings Limited | Polyurethane foams |
| ZA755593B (en) * | 1975-04-09 | 1976-08-25 | M & T Chemicals Inc | Polyurethane foams and compositions and processes for preparing rigid urethane foams |
| DE2945986A1 (de) * | 1978-11-16 | 1980-06-04 | Bridgestone Tire Co Ltd | Sicherheits-tank und verfahren zu dessen herstellung |
| US4607064A (en) * | 1983-05-16 | 1986-08-19 | The Dow Chemical Company | Polyurethane and urethane-modified isocyanurate foams and a polyol composition useful in their preparation |
| GB8531180D0 (en) * | 1985-12-18 | 1986-01-29 | Ici Plc | Cocatalyst systems |
-
1991
- 1991-04-19 AU AU78589/91A patent/AU7858991A/en not_active Abandoned
- 1991-04-19 HU HU9400541A patent/HUT68199A/hu active IP Right Revival
- 1991-04-19 EP EP19910909352 patent/EP0615526A4/fr not_active Withdrawn
- 1991-04-19 CA CA002119882A patent/CA2119882A1/fr not_active Abandoned
- 1991-04-19 BR BR9107331A patent/BR9107331A/pt not_active IP Right Cessation
- 1991-04-19 WO PCT/US1991/002799 patent/WO1992016574A1/fr not_active Ceased
- 1991-04-22 MY MYPI91000689A patent/MY106388A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0615526A1 (fr) | 1994-09-21 |
| WO1992016574A1 (fr) | 1992-10-01 |
| EP0615526A4 (fr) | 1994-11-17 |
| MY106388A (en) | 1995-05-30 |
| AU7858991A (en) | 1992-10-21 |
| BR9107331A (pt) | 1995-06-13 |
| HUT68199A (en) | 1995-05-29 |
| HU9400541D0 (en) | 1994-07-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4417001A (en) | Low smoke isocyanurate modified urethane foam and method of making same | |
| US5064872A (en) | Polyisocyanurate foam with chloropropane blowing agent | |
| CA2725334C (fr) | Procede pour la fabrication de mousses de polyisocyanurate rigides a l'aide de polyols d'huile naturelle | |
| CA2573709C (fr) | Systeme de mousse de polyurethane en vaporisateur gonflee a l'eau | |
| EP1115771B1 (fr) | Mousse de polyurethane rigide et element de construction d'isolation thermique comprenant cette mousse | |
| WO2013082963A1 (fr) | Mousses et articles fabriqués à partir de mousses contenant des agents gonflants hcfo ou hfo | |
| KR102065299B1 (ko) | 준불연 단열재 및 이의 제조방법 | |
| JP2010184974A (ja) | 耐火断熱被覆材 | |
| US20220073691A1 (en) | Flame retardant composition for polyurethane foam and flame-retarded polyurethane foam containing the same | |
| CA1062850A (fr) | Mousses de polyurethane de type isocyanurate, stables a temperature elevee, rigides et cellulaires | |
| CN113015757A (zh) | 不燃性聚氨酯泡沫用发泡性组合物 | |
| JP2013511589A (ja) | 良好な難燃特性を有する中密度装飾成形フォームの減少した成形時間での製造方法、難燃剤組成物および該方法により製造されたフォーム | |
| KR102190353B1 (ko) | 발포성 차열도료를 포함하는 고난연 단열재 및 이의 제조방법 | |
| KR20090052389A (ko) | 1,1,1,3,3-펜타플루오로부탄 및 1,1,1,2,3,3,3-헵타플루오로프로판을 포함하는 혼합물들 | |
| BR0115467B1 (pt) | processo para produzir uma espuma de poliuretano rÍgida de baixa densidade, espuma de poliuretano rÍgida e painel isolante tÉrmico. | |
| US5010116A (en) | Water blown foam | |
| Ashida et al. | Thermosetting foams | |
| US5026737A (en) | Process for the production of urethane-modified polyisocyanurate foam | |
| KR0184631B1 (ko) | 개질된 폴리이소시아누레이트 발포체, 이의 제조방법 및 이를 함유하는 폴리올 조성물 | |
| EP1209181B1 (fr) | Mousse de polyisocyanurate modifiée par uréthane | |
| US4636530A (en) | Isocyanate terminated quasi-prepolymers useful for preparing urethane-group-containing polyisocyanurate foams having low friability | |
| WO1992016574A1 (fr) | Mousse obtenue par expansion aqueuse | |
| KR100795768B1 (ko) | 발포성 코팅을 이용한 내화성 절연 건축용 패널 | |
| KR102065251B1 (ko) | 준불연 단열재의 제조방법 | |
| KR20120074560A (ko) | 수발포 폴리이소시아누레이트 폴리우레탄 발포체 조성물 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |