Claims
- 1. Process for tanning or retanning hide, skin or leather, characterized in that hide, skin or leather are treated with an aqueous liquor which contains:
- (a) optionally methylolated hydrophilic oligourethanes which have a molecular weight of from 300 to 20,000, characterized in that the oligourethanes have no free NCO groups, no aziridine groups, no phenolic groups, and no ionic groups; and, optionally,
- (b) formaldehyde or a substance from which formaldehyde may be split off.
- 2. Process according to claim 1, characterized in that the oligourethane molecule contains hydrophilic polyether segments.
- 3. A process for tanning or retanning a substrate selected from the group consisting of animal pelts and leather comprising treating the substrate with an aqueous liquor containing hydrophilic oligourethanes which have a molecular weight (M.sub.n) of from 300 to 20,000, characterized in that the oligourethanes have no free NCO groups, no aziridine groups, no phenolic groups, and no ionic groups.
- 4. The process of claim 3 wherein the oligourethanes are methylolated.
- 5. The process of claim 4 wherein the aqueous liquor contains from 0 to 100 wt. % based on oligourethane solids of compounds selected from the group consisting of formaldehyde and compounds which split off formaldehyde.
- 6. The process of claim 5 wherein the formaldehyde supplying compounds are present in amounts of about 0.5 to 30 wt. % based on oligourethane solids.
- 7. The process of claim 3 wherein the oligourethanes are present in the form of an aqueous dispersion with an average particule size of less than about 200 m.mu..
- 8. The process of claim 3 wherein the oligourethanes are water soluble.
- 9. A process for tanning or retanning a substrate selected from the group consisting of animal pelts and leather comprising treating the substrate with an aqueous liquor containing hydrophilic oligourethanes which have a molecular weight (M.sub.n) of from 300 to 20,000 and contain no free NCO groups, no aziridine groups, no phenolic groups, and no ionic groups, said hydrophilic oligourethanes synthesized by a process comprising:
- (a) reacting polyhydroxyl compounds selected from the group consisting of polyethers, polyesters and polycarbonates with
- (b) polyisocyanates, and
- (c) optionally chain-terminating agents.
- 10. The process of claim 9 wherein the NCO/OH ratio maintained during the synthesis of the hydrophilic oligourethanes is between 0.4 to 0.8.
- 11. The process of claim 9 wherein chain-terminating agents selected from the group consisting of polyols, amino alcohols and polyamines are used in the synthesis of the hydrophilic oligourethanes and wherein the NCO/OH ratio maintained during the synthesis reaction is between 0.4 to 0.8.
- 12. The process of claim 9 wherein chain-terminating agents selected from the group consisting of monofunctional alcohols, monofunctional amines, monofunctional carboxylic acids, urea and monofunctional isocyanates are used in the synthesis of the hydrophilic oligourethanes and wherein the NCO/OH maintained during the synthesis reaction is between 0.6 to 1.0.
- 13. The process of claim 12 wherein the chain-terminating agents are selected from the group consisting of monofunctional alcohols, monofunctional amines, monofunctional carboxylic acids and urea.
- 14. The process of claim 9 wherein chain-terminating agents are used in the synthesis of the hydrophilic, oligourethanes, at least one of said chain-terminating agents selected from the group consisting of polyols, amino alcohols and polyamines.
- 15. The process of claim 9 wherein the polyhydroxyl compounds are polyethers.
- 16. The process of claim 15 wherein the polyethers contain at least 50% by weight of ethylene oxide units and have a molecular weight of about 100 to 3,000.
Priority Claims (2)
Number |
Date |
Country |
Kind |
2416485 |
Apr 1974 |
DEX |
|
2504081 |
Jan 1975 |
DEX |
|
Parent Case Info
This is a continuation-in-part of copending application Ser. No. 561,809, filed Mar. 25, 1975, now abandoned.
US Referenced Citations (4)
Foreign Referenced Citations (2)
Number |
Date |
Country |
1,223,458 |
Jan 1959 |
FRX |
1,022,749 |
Jun 1955 |
DEX |
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
561809 |
Mar 1975 |
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