Claims
- 1. A process for the production of an optionally cellular, polyurethane elastomer or an optionally cellular, rigid structural polyurethane by reacting a reaction mixture comprising
- (i) a polyisocyanate,
- (ii) a high molecular weight polymer having at least two hydroxy groups and a molecular weight of 400 to about 10,000,
- (iii) up to about 150% by weight, based on the weight of component (ii) of a chain extender having at least two hydroxy groups and
- (iv) about 0.05 to 10% by weight, based on the weight of components (ii) and (iii), of a salt based on a carboxy functional siloxane and an amidine group-containing compound of the formula ##STR10## wherein R.sub.1, R.sub.2 and R.sub.3 are straight or branched, saturated or unsaturated hydrocarbon chains having up to 30 carbon atoms which may optionally be substituted by ether groups, ester groups, amide groups or amidine groups and may also optionally be terminated by isocyanate-reactive groups,
- R.sub.4 corresponds to the definition of R.sub.1, R.sub.2 and R.sub.3, but may additionally represent an aromatic substituent having 6 to 15 carbon atoms or may represent the group --NR.sub.2 R.sub.3 and
- R.sub.1, R.sub.2, R.sub.3 and R.sub.4 may, with one or both of the amidine nitrogens, also form a heterocyclic ring.
- 2. The process of claim 1 wherein the reaction mixture is processed as a one-shot system by the RlM process using an isocyanate index of about 70 to 120.
- 3. The process of claim 1 wherein reaction mixture additionally comprises a salt of an aliphatic carboxylic acid and a primary amine or a primary, secondary or tertiary amine containing an amide or an ester group.
- 4. The process of claim 1 wherein said reaction mixture additionally contains a tertiary amine-containing, isocyanate-reactive compound corresponding to the formula ##STR11## wherein R.sub.6 is a straight or branched alkyl radical having 1 to 4 carbon atoms,
- R.sub.7 is an alkylene, dialkylene ether or polyether diradical,
- R.sub.8 is a straight or branched, saturated or unsaturated hydrocarbon chain having up to 30 carbon atoms which may optionally be substituted by ether, ester or amide groups,
- x is independently a number of about 1 to 50,
- y and z are independently 0, 1 or 2 with the proviso that y+z must be at least 1.
- 5. The process of claim 3 wherein said reaction mixture additionally contains a tertiary amine-containing, isocyanate-reactive compound corresponding to the formula ##STR12## wherein R.sub.6 is a straight or branched alkyl radical having 1 to 4 carbon atoms,
- R.sub.7 is an alkylene, dialkylene ether or polyether diradical,
- R.sub.8 is a straight or branched, saturated or unsaturated hydrocarbon chain having up to 30 carbon atoms which may optionally be substituted by ether, ester or amide groups,
- x is independently a number of about 1 to 50,
- y and z are independently 0, 1 or 2 with the proviso that y +z must be at least 1.
- 6. The process of claim 1 wherein said amidine group containing compound corresponds to the formula ##STR13## wherein R.sub.4 contains a saturated or unsaturated fatty group and
- R.sub.3 is as previously defined above.
- 7. The process of claim 3 wherein said salt is the tall oil farty acid salt of the amide group-containing amine obtained by reacting N,N-dimethylamino-propylamine with tall oil fatty acid.
- 8. A process for the production of an optionally cellular, polyurethane elastomer or an optionally cellular, rigid structural polyurethane by reacting a reaction mixture comprising
- (i) a polyisocyanate,
- (ii) a high molecular weight polymer having at least two hydroxy groups and a molecular weight of 400 to about 10,000,
- (iii) about 5 to 150% by weight, based on the weight of component (ii) of a chain extender having at least two hydroxy groups and
- a mold release agent mixture comprising, based on the weight of component (ii) and (iii),
- (iv) about 0.05 to 10% by weight, of a salt based on a carboxy functional siloxane and an amidine group-containing compound of the formula ##STR14## wherein R.sub.1, R.sub.2 and R.sub.3 are straight or branched, saturated or unsaturated hydrocarbon chains having up to 30 carbon atoms which may optionally be substituted by ether groups, ester groups, amide groups or amidine groups and may also optionally be terminated by isocyanate-reactive groups,
- R.sub.4 corresponds to the definition of R.sub.1, R.sub.2 and R.sub.3, but may additionally represent an aromatic substituent having 6 to 15 carbon atoms or may represent the group --NR.sub.2 R.sub.3 and
- R.sub.1, R.sub.2, R.sub.3 and R.sub.4 may, with one or both of the amidine nitrogens, also form a heterocyclic ring,
- (v) a salt of an aliphatic carboxylic acid and a primary amine or a primary, secondary or tertiary amine containing an amide or an ester group and
- (vi) a tertiary amine-containing, isocyanate-reactive compound corresponding to the formula ##STR15## wherein R.sub.6 is a straight or branched alkyl radical having 1 to 4 carbon atoms,
- R.sub.7 is an alkylene, dialkylene ether or polyether diradical,
- R.sub.8 is a straight or branched, saturated or unsaturated hydrocarbon chain having up to 30 carbon atoms which may optionally be substituted by ether, ester or amide groups,
- x is independently a number of about 1 to 50,
- y and z are independently 0, 1 or 2 with the proviso that y +z must be at least 1.
- 9. The process of claim 8 wherein the reaction mixture is processed as a one-shot system by the RIM process using an isocyanate index of about 70 to 120.
- 10. The process of claim 8 wherein said amidine group-containing compound corresponds to the formula ##STR16## wherein R.sub.4 contains a saturated or unsaturated fatty group and
- R.sub.3 is as previously defined above.
- 11. The process of claim 8 wherein said salt is a tall oil fatty acid salt of the amide group-containing amine obtained by reacting N,N-dimethylaminopropylamine with tall oil fatty acid.
CROSS-REFERENCE TO RELATED APPLICATION
The present application is a continuation-in-part of U.S. Application Ser. No. 006,529 filed on Jan. 23, 1987.
US Referenced Citations (5)
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
6529 |
Jan 1987 |
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