GB1287781A - Process for the manufacture of polyurethane foams - Google Patents
Process for the manufacture of polyurethane foamsInfo
- Publication number
- GB1287781A GB1287781A GB44262/69A GB4426269A GB1287781A GB 1287781 A GB1287781 A GB 1287781A GB 44262/69 A GB44262/69 A GB 44262/69A GB 4426269 A GB4426269 A GB 4426269A GB 1287781 A GB1287781 A GB 1287781A
- Authority
- GB
- United Kingdom
- Prior art keywords
- molar proportions
- reacting
- prepared
- mols
- och
- 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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
-
- 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
- C08G18/4286—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones prepared from a combination of hydroxycarboxylic acids and/or lactones with polycarboxylic acids or ester forming derivatives thereof and polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences
-
- 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
- C08G2110/0008—Foam properties flexible
-
- 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
- C08G2110/0041—Foam properties having specified density
-
- 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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/06—Polyurethanes from polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2483/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Silicon Polymers (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
1287781 Polyurethane foams INTER - POLYMER RESEARCH CORP 8 Sept 1969 [11 Oct 1968] 44262/69 Headings C3C C3R and C3T [Also in Division C2] Flexible polyurethane foams having good humid ageing properties are prepared by reacting together a liquid polyester containing from 10 to 72% by weight of the epsilon-oxycaproyl unit [-O(CH 2 ) 5 CO-], at least one organic polyisocyanate, at least one blowing agent, at least one catalyst and at least one surfactant comprising a water-soluble or partially watersoluble polysiloxane-polyester block copolymer. Suitable liquid polyesters are prepared by reacting epsilon-caprolactone, 6-hydroxycaproic acid or an oligomer thereof with a dicarboxylic acid (e.g. adipic, succinic, glutaric, pimelic, azelaic or sebacic acid) or an anhydride thereof, an alkylene glycol (e.g. ethylene, propylene, diethylene, dipropylene, 1,3-butylene or neopentylene glycol) and a triol or tetrol branching agent (e.g. glycerol, 1,2,6-hexanetriol, trimethylolpropane, pentaerythritol or alphamethylglucoside) at temperatures of from 100‹ to 300‹ C. in presence of a polyesterification or ester interchange catalyst. Examples 3 to 10 describe the detailed preparation of suitable liquid polyesters. Suitable polyisocyanates are 2,4- and 2,6-toluene diisocyanates and mixtures thereof, diphenylmethane diisocyanates and mixtures thereof with their corresponding carbodiimide derivatives, and polymeric isocyanates of aniline/formaldehyde or orthotoluidine/formaldehyde condensation products. Suitable blowing agents are water, or mixtures thereof with halogenated aliphatic hydrocarbons or low boiling hydrocarbons. Exemplified catalysts are triethylenediamine, N-ethylmorpholine, N,N - dimethylhexadecylamine and N,N-dimethylbenzylamine. Suitable surfactants are prepared in Examples 12 to 15 and are: (12) a compound of the formula prepared by reacting CH 3 OCO(CH 2 ) 5 OCH 2 CH 2 OCH 2 CH 2 OCH 2 CH 2 OH with a methylhydrogen polysiloxane obtained by cohydrolysis from 8 molar proportions of methyldichlorosilane and 2 molar proportions of trimethylchlorosilane; (13) a compound of the formula prepared by reacting CH 2 : CHCH 2 OCO(CH 2 ) 5 (OCH 2 CH 2 ) 4 O.COCH 3 with a methylhydrogen polysiloxane as in (12); (14) a compound of the formula prepared by reacting a hydroxy-terminated polyester obtained from 1 mol. of 2-ethylhexanol, 5À5 mols. of tetraethylene-oxyglycol and 5À5 mols. of adipic acid, and a methylhydrogen polysiloxane obtained by cohydrolysis of 3 molar proportions of methyldichlorosilane, 15 molar proportions of dimethylchlorosilane and 2 molar proportions of trimethylchlorosilane ; and (15) a compound of the formula prepared by reacting a hydroxy-terminated polyester obtained from 1 mol. of 2-ethylhexanol, 2 mols. of epsilon-caprolactone and 8 mols. of ethylene oxide, and a methylhydrogen polysiloxane obtained by cohydrolysis of 3 molar proportions of methyldichlorosilane, 2 molar proportions of trimethylchlorosilane and 5 molar proportions of dimethylchlorosilane.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US76694568A | 1968-10-11 | 1968-10-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1287781A true GB1287781A (en) | 1972-09-06 |
Family
ID=25078004
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB44262/69A Expired GB1287781A (en) | 1968-10-11 | 1969-09-08 | Process for the manufacture of polyurethane foams |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1949307A1 (en) |
FR (1) | FR2022264A1 (en) |
GB (1) | GB1287781A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2119393A (en) * | 1982-04-08 | 1983-11-16 | Caligen Foam Ltd | Polyurethane foam |
-
1969
- 1969-09-08 GB GB44262/69A patent/GB1287781A/en not_active Expired
- 1969-09-30 DE DE19691949307 patent/DE1949307A1/en active Pending
- 1969-10-10 FR FR6934830A patent/FR2022264A1/fr not_active Withdrawn
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2119393A (en) * | 1982-04-08 | 1983-11-16 | Caligen Foam Ltd | Polyurethane foam |
Also Published As
Publication number | Publication date |
---|---|
DE1949307A1 (en) | 1970-04-16 |
FR2022264A1 (en) | 1970-07-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5672636A (en) | Production of low-fogging polyurethane foams, and specific poly-oxyalkylene-polyols which can be used for this purpose | |
EP0243832A3 (en) | Process for the preparation of elastomeric, compact or cellular polyurethane or polyurethane-polyurea moulded pieces | |
GB1303787A (en) | ||
GB1289517A (en) | ||
EP0449419B1 (en) | Hydroxy terminated polyamides | |
RU99111765A (en) | HARD FOAM POLYURETHANES | |
CA1281734C (en) | Process for the production of oligoesters containing hydroxy groups and their use | |
US6060531A (en) | Production of low-fogging polyurethane foams, and specific polyoxyalkylene-polyols which can be used for this purpose | |
US4383050A (en) | Process for the preparation of low temperature flexible polyurethane elastomers | |
US5093382A (en) | Preparation of foams using polyfunctional organic acids | |
US20160229972A1 (en) | Foam products and methods of producing the same | |
JP4620256B2 (en) | Open cell polyurethane rigid foam | |
US4256847A (en) | Rigid polyurethane foam process using lithium/zinc catalyst | |
CA1233949A (en) | Curable compositions for producing polyurethane foams | |
US5244931A (en) | Mixtures of dibasic acid esters and nonylphenol as cell openers in low density rigid polyurethanes useful in pour-behind-fabric applications of low density SRIM | |
EP0398304B1 (en) | Flexible polyurethane foams and process for preparing them | |
JPH01115927A (en) | Terephthalic ester polyol | |
US5114985A (en) | Dibasic acid esters as cell openers in low density rigid polyurethanes useful in pour-behind-fabric applications of low density SRIM | |
GB1287781A (en) | Process for the manufacture of polyurethane foams | |
WO1985000175A1 (en) | Low temperature, storage stable mixtures of prepolymers and flow modifiers | |
US4469616A (en) | Low temperature, storage stable mixtures of polyester prepolymers and flow modifiers | |
EP0269346A2 (en) | Polyurethane froth foam | |
GB1285340A (en) | Process for the manufacture of polyesters and polyurethane foams | |
JPH0676471B2 (en) | Method for manufacturing laminated foam | |
CA1266483A (en) | Polyester polyols and their use for preparing microcellular polyurethane elastomers |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |