GB1513807A - High-temperature resistant isocyanurate foams - Google Patents
High-temperature resistant isocyanurate foamsInfo
- Publication number
- GB1513807A GB1513807A GB42065/75A GB4206575A GB1513807A GB 1513807 A GB1513807 A GB 1513807A GB 42065/75 A GB42065/75 A GB 42065/75A GB 4206575 A GB4206575 A GB 4206575A GB 1513807 A GB1513807 A GB 1513807A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- reaction
- polyisocyanate
- polyol
- nco
- 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
Links
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
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
-
- 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
- C08G18/161—Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
-
- 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
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
-
- 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
- C08G2101/00—Manufacture of cellular products
-
- 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
-
- 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)
Abstract
1513807 Isocyanurate foams BASF WYANDOTTE CORP 14 Oct 1975 [24 Dec 1974] 42065/75 Heading C3R An isocyanurate foam is the reaction product of (a) a polyarylpolyalkylene polyisocyanate having a functionality of from 2À2 to 3À5 or an NCO -terminated prepolymer thereof (b) from 5 to 40 p.b.w. of a nitrogen-containing polyether polyol having a hydroxyl number of from 100- 900 and a nitrogen content of from 1-15% wt., (c) from 10-40 p.b.w. of a fluorocarbon blowing agent and (d) from 1-6 p.b.w. of a 1,3,5- tris(N,N - dialkylaminoalkyl) - S - hexahydrotriazine trimerization catalyst or the alkylene oxide and water adducts thereof, said parts being based on 100 p.b.w. of polyisocyanate. Preferred component (a) is a crude polyphenyl polymethylene polyisocyanate mixture having a viscosity of from 150-250 c.p.s. at 25‹ C., an NCO content of at least 31% wt. and having from 42-48% wt. of its NCO content present as a monomeric diphenylmethane diisocyanate; and is prepared by the phosgenation of anilineformaldehyde reaction products. The NCO- terminated prepolymer is prepared by reacting a stoichiometric excess of the polyaryl polyalkylene polyisocyanate with an organic compound having at least 2 reactive hydrogen atoms. Component (b) may be prepared by the reaction of an alkylene oxide with a compound selected from ammonia, alkylene polyamines, polyalkylene polyamines, primary alkylamines, primary aralkylamines and Mannich condensation products of a phenolic compound with formaldehyde and an alkanolamine. Optional ingredients include surfactants, fillers and pigments, and additional catalysts, e.g. catalysts which promote carbodiimide linkages, such as phospholene oxides, methyl alcohol, furfuryl alcohol, 2,4,6 - tris(dialkanolamino) - S - triazine and 2,4 - bis(dialkylamino) - 6 - N- (alkylhydroxyalkylamino) - )S - triazines, and urethane catalysts such as tertiary amines and metallo-organic salts. In the examples polyisocyanurate foams are prepared from the following formulations: (1) polyphenylpolymethylene isocyanate, trichlorofluoromethane, 1,3,5 - tris(dimethylaminopropyl) - hexahydrotriazine (TDH), a silicone surfactant, a polyol (OH number 530) prepared by the reaction of propylene oxide with the Mannich condensation product of HCHO, diethanolamine and a mixture of phenol and cresols, and either (a) bis(diethylamino) - N - methylhydroxyethanolamino - S triazine (DMT) and dibutyltin dilaurate (DBTL), or (b) furfuryl alcohol and either DBTL or dibutyltin diacetate; or (2) polyphenylpolymethylene - isocyanate, trichlorofluoromethane, TDH, DMT, DBTL, a silicone surfactant, and a polyol (OH number 450) prepared by the reaction of ethylene oxide with the propylene oxide adduct of ethylene diamine alone or in admixture with a polyol which is the ethylene oxide adduct of ethylene diamine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53609474A | 1974-12-24 | 1974-12-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1513807A true GB1513807A (en) | 1978-06-07 |
Family
ID=24137117
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB42065/75A Expired GB1513807A (en) | 1974-12-24 | 1975-10-14 | High-temperature resistant isocyanurate foams |
Country Status (10)
Country | Link |
---|---|
JP (1) | JPS5175800A (en) |
AU (1) | AU497306B2 (en) |
BE (1) | BE835625A (en) |
CA (1) | CA1044847A (en) |
DE (1) | DE2551809C3 (en) |
FR (1) | FR2295976A1 (en) |
GB (1) | GB1513807A (en) |
IT (1) | IT1060513B (en) |
NL (1) | NL7513046A (en) |
ZA (1) | ZA756433B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014113379A1 (en) * | 2013-01-15 | 2014-07-24 | Basf Se | Rigid foam |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53145900A (en) * | 1977-05-25 | 1978-12-19 | Kohkoku Chem Ind | Manufacture of urethaneemodified polyisocyanurate foam |
JPS5620020A (en) * | 1979-06-11 | 1981-02-25 | Upjohn Co | Polyol mixture |
-
1975
- 1975-10-13 ZA ZA6433A patent/ZA756433B/en unknown
- 1975-10-14 GB GB42065/75A patent/GB1513807A/en not_active Expired
- 1975-10-28 CA CA238,501A patent/CA1044847A/en not_active Expired
- 1975-11-04 AU AU86301/75A patent/AU497306B2/en not_active Expired
- 1975-11-06 NL NL7513046A patent/NL7513046A/en not_active Application Discontinuation
- 1975-11-14 DE DE2551809A patent/DE2551809C3/en not_active Expired
- 1975-11-17 BE BE1007009A patent/BE835625A/en not_active IP Right Cessation
- 1975-11-17 JP JP50137343A patent/JPS5175800A/ja active Pending
- 1975-11-18 FR FR7535164A patent/FR2295976A1/en active Granted
- 1975-11-18 IT IT52263/75A patent/IT1060513B/en active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014113379A1 (en) * | 2013-01-15 | 2014-07-24 | Basf Se | Rigid foam |
US9745408B2 (en) | 2013-01-15 | 2017-08-29 | Basf Se | Rigid foam |
Also Published As
Publication number | Publication date |
---|---|
DE2551809C3 (en) | 1979-09-20 |
FR2295976B1 (en) | 1981-03-27 |
NL7513046A (en) | 1976-06-28 |
AU497306B2 (en) | 1978-12-07 |
AU8630175A (en) | 1977-05-12 |
CA1044847A (en) | 1978-12-19 |
IT1060513B (en) | 1982-08-20 |
DE2551809B2 (en) | 1978-08-03 |
JPS5175800A (en) | 1976-06-30 |
DE2551809A1 (en) | 1976-07-01 |
BE835625A (en) | 1976-05-17 |
ZA756433B (en) | 1977-01-26 |
FR2295976A1 (en) | 1976-07-23 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19921014 |