GB1476830A - Process for the preparation of polyurethanes - Google Patents
Process for the preparation of polyurethanesInfo
- Publication number
- GB1476830A GB1476830A GB2735175A GB2735175A GB1476830A GB 1476830 A GB1476830 A GB 1476830A GB 2735175 A GB2735175 A GB 2735175A GB 2735175 A GB2735175 A GB 2735175A GB 1476830 A GB1476830 A GB 1476830A
- Authority
- GB
- United Kingdom
- Prior art keywords
- adduct
- propylene
- metallic
- catalyst
- bis
- 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/1808—Catalysts containing secondary or tertiary amines or salts thereof having alkylene polyamine 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
1476830 Polyurethanes RHONE POULENC INDUSTRIES 27 June 1975 [28 June 1974] 27351/75 Heading C3R A process for the preparation of a foamed or unfoamed polyurethane comprises reacting an organic polyol and an organic polyisocyanate in the presence of a catalyst comprising bis -N- (6 - dimethylaminohexyl) methylamine, generally in an amount of from 1 x 10<SP>-3</SP> to 3000 x 10<SP>-3</SP> mol per mol of polyol, and optionally a metallic or organo-metallic catalyst, the ratio of the number of metal atoms of the said metallic catalyst to the number of tertiary nitrogen atoms of the said amine catalyst generally being from 0À1 to 1. Suitable metallic catalysts are dibutyl tin dilaurate, stannic chloride, stannous octate, stannous oleate, dibutyltin bis-(2-ethyl hexoate), ferric chloride, cobalt benzoate and cobalt 2-ethylhexoate. The polyisocyanate can be any conventional aromatic, aliphatic or cycloaliphatic diisocyanate or a prepolymer. Suitable polyols are polyhydric polyethers, polyesters, polyesteramides, polyurethanes or hydrocarbons, or optionally modified caster oil, or a silanol or siloxane etherified with a polyhydric polyether or polyester. The reaction mixture may also comprise trimerization catalysts e.g. alkali metal salts of phenols or an alkali metal hydroxide; catalysts for the formation of carbodiimide groups e.g. phospholines and phospholine oxides; regulators of the urethane-forming reaction e.g. malonitrile, acetylacetone and benzoylacetone; conventional foaming agents and surfactants and other additives. In the Examples foams are prepared from reaction mixtures comprising bis-N- (6 - dimethylaminohexyl) methylamine in dipropylene glycol, a siloxane/alkylene oxide block copolymer surfactant, either a polyisocyanate obtained by the phosgenation of an aniline-formaldehyde condensate consisting mainly of 4,4<SP>1</SP>-diisoocyanato-diphenylmethane, or tolylene diisoocyanate and either (1) water, fluorotrichloromethane and a polyol mixture consisting of an adduct of propylene and ethylene oxides to a mixture of sucrose and propylene glycol, and an ethylene oxide/triethanol-amine adduct; or (2) fluorotrichloromethane and a propylene oxide/ glycol glucoside adduct; or (3) water, stannous octoate and an adduct of ethylene and propylene oxides to glycerol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7422588A FR2276333A1 (en) | 1974-06-28 | 1974-06-28 | PROCESS FOR PREPARING POLYURETHANNES IN THE PRESENCE OF BIS (DIMETHYLAMINOHEXYL-6) METHYLAMINE |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1476830A true GB1476830A (en) | 1977-06-16 |
Family
ID=9140650
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2735175A Expired GB1476830A (en) | 1974-06-28 | 1975-06-27 | Process for the preparation of polyurethanes |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE830747A (en) |
CH (1) | CH593308A5 (en) |
DE (1) | DE2528657A1 (en) |
FR (1) | FR2276333A1 (en) |
GB (1) | GB1476830A (en) |
IT (1) | IT1039540B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4080343A (en) * | 1976-09-22 | 1978-03-21 | Abbott Laboratories | Polyurethane catalyst |
-
1974
- 1974-06-28 FR FR7422588A patent/FR2276333A1/en active Granted
-
1975
- 1975-06-27 GB GB2735175A patent/GB1476830A/en not_active Expired
- 1975-06-27 DE DE19752528657 patent/DE2528657A1/en not_active Withdrawn
- 1975-06-27 BE BE157769A patent/BE830747A/en not_active IP Right Cessation
- 1975-06-27 IT IT2492175A patent/IT1039540B/en active
- 1975-06-27 CH CH838375A patent/CH593308A5/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
IT1039540B (en) | 1979-12-10 |
FR2276333B1 (en) | 1978-03-31 |
BE830747A (en) | 1975-12-29 |
CH593308A5 (en) | 1977-11-30 |
FR2276333A1 (en) | 1976-01-23 |
DE2528657A1 (en) | 1976-01-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |