IP Library Granted Patent US 11,267,926
Granted Patent B2
US 11,267,926 · App. 16/346,715 · Granted Mar 8, 2022

Low-damping polyurethane elastomer

Inventors: Johannes Poppenberg (Wyandotte, MI); Waldemar Meier (Lemfoerde, DE); Christina Tepper (Lemfoerde, DE); Markus Susoff (Kassel, DE); Dejan Petrovic (Lemfoerde, DE); Steffen Richter (Lemfoerde, DE)
Assignee: BASF SE
C08G18/12C08G18/3228C08G18/3246C08G18/4018C08G18/4238C08G18/4277C08G18/4854C08G18/7642C08G18/7678C08G18/797C08J9/125C08G2110/005C08G2110/0008C08G2110/0066C08G2110/0083C08G2350/00C08G2410/00C08J2203/10C08J2205/044C08J2375/12
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Quick Facts
Patent No.
US 11,267,926
App. No.
16/346,715
Granted
Mar 8, 2022
Kind
B2
Abstract

The present invention relates to a method of preparing a polyurethane elastomer, said method comprising the step of reacting at least one isocyanate composition (ZI) and one polyol composition (ZP) comprising a poly-ε-caprolactone polyol and an α-hydro-ω-hydroxy-poly(oxytetramethylene) polyol to obtain an isocyanate-functional prepolymer and the step of reacting the prepolymer obtained as per step (i) with at least one chain extender (KV). The present invention further relates to a polyurethane elastomer obtained or obtainable according to a method of the invention and also to the method of using a polyurethane elastomer according to the invention or a polyurethane elastomer obtained or obtainable according to a method of the invention in the manufacture of a shaped article, especially a damping element, a shock absorber or a stop buffer or part of a shoe or of a shoe sole, for example part of an insert sole or of a midsole.

Claims (24)

1. A method of preparing a polyurethane elastomer, comprising (i) and (ii):

(i) reacting at least one isocyanate composition (ZI) and one polyol composition (ZP) comprising a poly-ε-caprolactone polyol and an α-hydro-ω-hydroxypoly(oxytetramethylene) polyol to obtain an isocyanate-functional prepolymer, and

(ii) reacting the prepolymer obtained in (i) with at least one chain extender (KV) in the presence of a blowing agent.

2. The method according to claim 1 , wherein the reacting in (i) is performed such that the prepolymer obtained in (i) has an isocyanate (NCO) content in the range from 2% to 8%.

3. The method according to claim 1 , wherein the reacting in (i) is effected at a temperature in the range from 110° C. to 180° C.

4. The method according to claim 1 , wherein the reacting in (i) is performed such that the prepolymer obtained in (i) has an isocyanate (NCO) content in the range from 8% to 22%.

5. The method according to claim 1 , wherein the reacting in (i) is effected at a temperature in the range from 40° C. to 110° C.

6. The method according to claim 1 , wherein the reacting in (ii) is performed in the presence of at least further component selected from the group consisting of a polyol, water, a chain-extending agent, a crosslinking agent, a catalyst, and an auxiliary.

7. The method according to claim 1 , wherein the poly-ε-caprolactone polyol is obtained by reacting ε-caprolactone and a starter molecule that is a diol having a number average molecular weight in the range from 80 to 1500 g/mol.

8. The method according to claim 1 , wherein the poly-ε-caprolactone polyol is obtained by reacting ε-caprolactone and at least one starter molecule selected from the group consisting of an α-hydro-ω-hydroxypoly(oxytetramethylene)diol, a polyethylene glycol and a polypropylene glycol.

9. The method according to claim 1 , wherein the polyol composition comprises the α-hydro-ω-hydroxypoly(oxytetramethylene) polyol in an amount in the range from 0.1 to 50 wt %, based on the polyol composition.

10. The method according to claim 1 , wherein the isocyanate composition comprises at least one isocyanate selected from the group consisting of 1,5-naphthylene diisocyanate (NDI), 4,4′-diphenylmethane diisocyanate (MDI), p-phenyl diisocyanate (PPDI) and o-tolidine diisocyanate (TODI).

11. The method according to claim 1 , wherein the isocyanate composition comprises 1,5-naphthylene diisocyanate (NDI) in an amount ranging from 90 to 100 wt % based on the entire isocyanate composition.

12. The method according to claim 1 , wherein the chain extender (KV) is at least one selected from the group consisting of water, a diol having a molecular weight in the range from 50 to 500 g/mol, a triol having a molecular weight in the range from 50 to 500 g/mol and a diamine having a molecular weight in the range from 50 to 500 g/mol.

13. The method according to claim 1 , wherein the poly-ε-caprolactone polyol and/or the α-hydro-ω-hydroxypoly(oxytetramethylene) polyol have a number average molecular weight in the range from 1500 to 2500 g/mol.

14. A polyurethane elastomer obtained by a method that comprises (i) and (ii):

(i) reacting at least one isocyanate composition (ZI) and one polyol composition (ZP) comprising a poly-ε-caprolactone polyol and an α-hydro-ω-hydroxypoly(oxytetramethylene) polyol to obtain an isocyanate-functional prepolymer, and

(ii) reacting the prepolymer obtained in (i) with at least one chain extender (KV) in the presence of a blowing agent.

15. The polyurethane elastomer according to claim 14 wherein the polyurethane elastomer is microcellular.

16. The polyurethane elastomer according to claim 14 having a density in the range from 0.12 to 0.8 g/cm 3 according to DIN EN ISO 845.

17. A shaped article comprising the polyurethane elastomer according to claim 14 .

18. The shaped article according to claim 17 , which is a damping element, a shock absorber, a stop buffer, or part of a shoe.

19. The method according to claim 1 , wherein the (Z1) component consists of 1,5-napththylene diisocyanate and the polyol component (ZP) consists of poly-ε-caprolactone polyol and α-hydro-ω-hydroxypoly(oxytetramethylene) polyol.

20. The method according to claim 19 , wherein the polyol component (ZP) comprises 15-25% by weight of α-hydro-ω-hydroxy-poly(oxytetramethylene).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2019
From: POPPENBERG, JOHANNES; MEIER, WALDEMAR; TEPPER, CHRISTINA; SUSOFF, MARKUS; PETROVIC, DEJAN; RICHTER, STEFFEN
To: BASF POLYURETHANES GMBH
Reel/Frame 049130/0803 →
Priority Claims (1)
EP 16198630 · Nov 14, 2016 · regional
Continuity (1)
Related Publication 20190276582A1 · Sep 12, 2019