GB909358A - Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds - Google Patents
Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compoundsInfo
- Publication number
- GB909358A GB909358A GB1923860A GB1923860A GB909358A GB 909358 A GB909358 A GB 909358A GB 1923860 A GB1923860 A GB 1923860A GB 1923860 A GB1923860 A GB 1923860A GB 909358 A GB909358 A GB 909358A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- compounds
- carboxylic acids
- acid
- include those
- 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
- C08G18/222—Catalysts containing metal compounds metal compounds not provided for in groups C08G18/225 - C08G18/26
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)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A process for the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds is characterized in that the reaction is carried out in the presence of a mercury salt of a carboxylic acid. Salts listed include those of monocarboxylic acids; dimethylglycine or 6-dimethylaminocaproic acid; di- or tri-carboxylic acids such as the reaction products of polyoxyalkylene diols or triols with two or three molecular proportions, respectively, of maleic or succinic anhydride; N,N1-ethylenediamine tetracarboxylic acid; carboxylic acids containing aromatic nuclei; and cycloaliphatic carboxylic acids. Polyesters, polyesteramides, polyethers and mixtures thereof are suitable hydroxy compounds. The polyethers include those obtained from cyclic oxides having a functionality greater than two. The mercury salts can be used together with tertiary amine catalysts, soluble organic compounds of metals such as iron or manganese acetylacetonate antimony compounds, or dibutyl tin dilaurate or stannous octoate. The reaction mixture may also contain antioxidants, such as tert. butyl catechol, surface-active agents, flame-retardants such as trichloroethyl phosphate and antimony oxide, plasticizers such as tricresyl phosphate and dioctyl phthalate and carbon black, silica, colour stabilizers and whitening agents. The examples describe the preparation of cellular products.ALSO:A process for the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds is characterised in that the reaction is carried out in the presence of a mercury salt of a carboxylic acid. The process is applicable to the preparation of cellular products, in one preferred embodiment by the simultaneous interaction of a secondary hydroxyl-ended polymer, especially a polyether, an organic polyisocyanate and water and/or a low boiling liquid in the presence of the mercury salt. Salts listed include those of monocarboxylic acids; dimethylglycine or 6-dimethylaminocaproic acid; di-or tri-carboxylic acids such as the reaction products of polyoxyalkylene diols or triols with two or three molecular proportions, respectively, of maleic or succinic anhydride; N, N1-ethylenediamine-tetracarboxylic acid; carboxylic acids containing aromatic nuclei; and cycloaliphatic carboxylic acids. Polyesters, polyester amides, polyethers and mixtures thereof are suitable hydroxy compounds. The polyethers include those obtained from cyclic oxides having a functionality greater than two. The tin salts can be used together with tertiary amine catalysts, soluble organic compounds of metals such as iron or manganese acetyl-acetonate, antimony compounds or dibutyl tin dilaurate or stannous octoate. The reaction mixture may also contain antioxidants such as tert butyl catechol, surface-active agents, flame retardants such as trichlorethyl phosphate and antimony oxide, plasticizers such as tricresyl phosphate and dioctyl phthalate, and carbon black, silica, colour stabilizers and whitening agents. In a typical example, (4) a mixture polypropylene glycol and oxypropylated trimethylolpropane, blended together with triethylene diamine, N-dimethylbenzylamine, mercury salt of octoic acid, alkylsilane-polyoxyalkylene block copolymer and water, is converted to a cellular product by blending with tolylene -2 : 4-and 2 : 6-diisocyanates. In other examples the salt used is the 2-ethylhexoate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1923860A GB909358A (en) | 1960-05-31 | 1960-05-31 | Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1923860A GB909358A (en) | 1960-05-31 | 1960-05-31 | Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB909358A true GB909358A (en) | 1962-10-31 |
Family
ID=10126009
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1923860A Expired GB909358A (en) | 1960-05-31 | 1960-05-31 | Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB909358A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3395108A (en) * | 1964-09-30 | 1968-07-30 | Allied Chem | Manufacture of filled urethane elastomers cured with a mixture of polyol, inert fille, mercuric salt of an aliphatic monocarboxylic acid and a basic metal compound |
US3419509A (en) * | 1965-11-22 | 1968-12-31 | Wyandotte Chemicals Corp | Mercury compounds as catalysts for the polyurethane reaction |
US3492255A (en) * | 1966-07-07 | 1970-01-27 | Allied Chem | Noncellular rapidly gelled polyurethane compositions |
US3670070A (en) * | 1968-12-17 | 1972-06-13 | Usm Corp | Processes for molding polyurethane foam articles |
GB2133413A (en) * | 1982-12-20 | 1984-07-25 | Basf Wyandotte Corp | Preparation of noncellular polyurethane elastomers |
US5064871A (en) * | 1989-07-19 | 1991-11-12 | Essex Specialty Products, Inc. | Latent catalysts comprising bismuth carboxylates and zirconium carboxylates |
-
1960
- 1960-05-31 GB GB1923860A patent/GB909358A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3395108A (en) * | 1964-09-30 | 1968-07-30 | Allied Chem | Manufacture of filled urethane elastomers cured with a mixture of polyol, inert fille, mercuric salt of an aliphatic monocarboxylic acid and a basic metal compound |
US3419509A (en) * | 1965-11-22 | 1968-12-31 | Wyandotte Chemicals Corp | Mercury compounds as catalysts for the polyurethane reaction |
US3492255A (en) * | 1966-07-07 | 1970-01-27 | Allied Chem | Noncellular rapidly gelled polyurethane compositions |
US3670070A (en) * | 1968-12-17 | 1972-06-13 | Usm Corp | Processes for molding polyurethane foam articles |
GB2133413A (en) * | 1982-12-20 | 1984-07-25 | Basf Wyandotte Corp | Preparation of noncellular polyurethane elastomers |
US5064871A (en) * | 1989-07-19 | 1991-11-12 | Essex Specialty Products, Inc. | Latent catalysts comprising bismuth carboxylates and zirconium carboxylates |
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