GB1033928A - Improvements in or relating to the manufacture of polyurethanes - Google Patents
Improvements in or relating to the manufacture of polyurethanesInfo
- Publication number
- GB1033928A GB1033928A GB3302762A GB3302762A GB1033928A GB 1033928 A GB1033928 A GB 1033928A GB 3302762 A GB3302762 A GB 3302762A GB 3302762 A GB3302762 A GB 3302762A GB 1033928 A GB1033928 A GB 1033928A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mixture
- oxide
- weight
- lead
- reaction product
- 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
- C08G18/22—Catalysts containing metal compounds
- C08G18/26—Catalysts containing metal compounds of lead
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
A composition for use in polyurethane production consists of a mixture of lead octoate and a reaction product of an alkylene oxide with an active hydrogen-containing compound, said mixture containing from 0.5 to 5.0 parts by weight of said reaction product for each part by weight of lead octoate. Preferred alkylene oxide reaction products are those derived from triethanolamine or triisopropanolamine with propylene oxide, block copolymers of ethylene oxide and propylene oxide and reaction products of octyl or nonyl phenol with 2-8 moles of ethylene oxide. The composition may be mixed with a polyhydroxy compound and reacted with an organic polyisocyanate to form a cellular or homogeneous polyurethane. Polyhydroxyl compounds may be polyesters, polyethers, polyesteramides. Conventional polyisocyanates are specified. In Examples (1) diphenylmethane diisocyanate was added to a mixture of oxypropylated trimethylolpropane, tri(b -chloroethyl)phosphate, siloxane block copolymer, FCCl3 and equal parts of lead 2-ethylhexoate and ethoxylated octyl phenol to produce a rigid foam (3) a mixture of equal parts of lead 2-ethylhexoate and ethoxylated octyl phenol was dissolved in propoxylated glycerol and the solution continuously mixed with more propoxylated glycerol, tolylene diisocyanate, triethylene diamine, water and siloxane. A foam resulted.ALSO:A catalytic composition comprises a mixture of lead octoate and a reaction product of an alkylene oxide with an active hydrogen-containing compound, said mixture containing from 0.5 to 5.0 parts by weight of said reaction product for each part by weight of lead octoate. Preferred alkylene oxide reaction products are those derived from triethanolamine or triisopropanolamine with propylene oxide, block copolymers of ethylene oxide and propylene oxide and reaction products of octyl or nonyl phenol with 2-8 moles of ethylene oxide. The composition may be mixed with a polyhydroxy compound and reacted with an organic polyisocyanate to from a cellular or homogeneous polyurethane.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3302762A GB1033928A (en) | 1962-08-28 | 1962-08-28 | Improvements in or relating to the manufacture of polyurethanes |
DE19631520125 DE1520125A1 (en) | 1962-08-28 | 1963-08-28 | Process for the production of polymeric substances |
FR945940A FR84481E (en) | 1962-08-28 | 1963-08-28 | Manufacturing process of polymeric materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3302762A GB1033928A (en) | 1962-08-28 | 1962-08-28 | Improvements in or relating to the manufacture of polyurethanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1033928A true GB1033928A (en) | 1966-06-22 |
Family
ID=10347551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3302762A Expired GB1033928A (en) | 1962-08-28 | 1962-08-28 | Improvements in or relating to the manufacture of polyurethanes |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1520125A1 (en) |
GB (1) | GB1033928A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3324054A (en) * | 1963-10-17 | 1967-06-06 | Int Lead Zinc Res | Production of polyurethane foams using arylleadtriester catalysts |
US6368714B1 (en) * | 1993-10-14 | 2002-04-09 | John Russell Robertson | Moisture-activated adhesive compositions |
-
1962
- 1962-08-28 GB GB3302762A patent/GB1033928A/en not_active Expired
-
1963
- 1963-08-28 DE DE19631520125 patent/DE1520125A1/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3324054A (en) * | 1963-10-17 | 1967-06-06 | Int Lead Zinc Res | Production of polyurethane foams using arylleadtriester catalysts |
US6368714B1 (en) * | 1993-10-14 | 2002-04-09 | John Russell Robertson | Moisture-activated adhesive compositions |
Also Published As
Publication number | Publication date |
---|---|
DE1520125A1 (en) | 1969-07-10 |
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