IP Library Granted Patent US 9,453,147
Granted Patent B2
US 9,453,147 · App. 14/350,999 · Granted Sep 27, 2016

Cold contact adhesives

Inventors: Harald Kraus (Leverkusen, DE); Wolfgang Arndt (Dormagen, DE); Matthias Wintermantel (Hürth, DE)
Assignee: Covestro Deutschland AG
C09J9/00B32B27/40C08G18/0823C08G18/0828C08G18/10C08G18/12C08G18/4202C08G2170/80C08G2170/90
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Quick Facts
Patent No.
US 9,453,147
App. No.
14/350,999
Granted
Sep 27, 2016
Kind
B2
Abstract

An aqueous dispersion comprising at least one polyurethane polymer with a melting temperature in the range of 30° C. to 50° C. and (cold contact) adhesives comprising such a polyurethane dispersion, a method for creating an adhesive bonding and the use of such (cold contact) adhesives for creating an adhesive bonding.

Claims (23)

1. An aqueous dispersion comprising at least one polyurethane polymer with a melting temperature in the range of 30° C. to 50° C. as determined by differential scanning calorimetry according to DIN 65467 at a heating rate of 20 K/min, the polyurethane polymer being obtained from a reaction mixture comprising:

AI) at least one polyester polyol with a number average molecular weight in the range of 400 g/mol to 5000 g/mol and a melting temperature in the range of 40° C. to 80° C. as determined by differential scanning calorimetry according to DIN 65467 at a heating rate of 20 K/min;

AII) at least one polyester polyol with a number average molecular weight in the range of 400 g/mol to 5000 g/mol and a melting temperature in the range of 5° C. to 35° C. as determined by differential scanning calorimetry according to DIN 65467 at a heating rate of 20 K/min;

B) optionally, at least one difunctional polyol component;

C) at least one aliphatic diisocyanate; and

D) at least one aminic chain extender comprising at least one ionic or potentially ionic group;

wherein

the molar ratio AI):AII) is in the range of 7:3 to 3:7.

2. The dispersion according to claim 1 , wherein the polyurethane polymer has a glass transition temperature in the range of −60° C. to −10° C. as determined by differential scanning calorimetry according to DIN 65467 at a heating rate of 20 K/min.

3. The dispersion according to claim 1 , wherein the polyester polyol AI) has a melting temperature in the range of 40° C. to 60° C. as determined by differential scanning calorimetry according to DIN 65467 at a heating rate of 20 K/min.

4. The dispersion according to claim 1 , wherein the polyester polyol AII) has a melting temperature in the range of 15° C. to 30° C. as determined by differential scanning calorimetry according to DIN 65467 at a heating rate of 20 K/min.

5. The dispersion according to claim 1 , wherein the molar ratio AI):AII) is in the range of 6:4 to 4:6.

6. The dispersion according to claim 1 , wherein the polyester polyol AI) has an enthalpy of fusion in the range of 65 J/g to 90 J/g as determined by differential scanning calorimetry according to DIN 65467 at a heating rate of 20 K/min.

7. The dispersion according to claim 1 , wherein the polyester polyol AII) has an enthalpy of fusion in the range of 30 J/g to 70 J/g as determined by differential scanning calorimetry according to DIN 65467 at a heating rate of 20 K/min.

8. The dispersion according to claim 1 , wherein the polyester polyols AI) and AII) are aliphatic.

9. The dispersion according to claim 1 , wherein the polyester polyol AI) is obtained from a reaction mixture comprising adipic acid and 1,4-butanediol or 1,6-hexanediol.

10. The dispersion according to claim 1 , wherein the polyester polyol AII) is obtained from a reaction mixture comprising adipic acid, 1,6-hexanediol and neopentyl glycol or from a reaction mixture comprising adipic acid, 1,4-butanediol and neopentyl glycol.

11. The dispersion according to claim 1 , wherein the aliphatic diisocyanate C) is selected from the group consisting of hexamethylene 1,6-diisocyanate, 1,3-bis(isocyanato-methyl)cyclohexane, 1,4-bis(isocyanato-methyl)cyclohexane, isophorone diisocyanate, 4,4′-diasocyanato-cyclohexyl)methane, 2,4′-di(isocyanato-cyclohexyl)methane, and mixtures thereof.

12. The dispersion according to claim 1 , wherein the aminic chain extender D) comprises a mixture of the sodium salt of N-(2-aminoethyl)-2-aminoethanesulfonic acid and diethanolamine or comprises a mixture of the sodium salt of N-(2-aminoethyl)-2-aminoethanesulfonic acid, diethanolamine and N-(2-hydroxyethyl)-ethylenediamine.

13. An adhesive comprising at least the dispersion according to claim 1 .

14. The adhesive according to claim 13 , wherein the adhesive is a cold contact adhesive.

15. A method comprising utilizing the dispersion according to claim 1 for bonding of rubber materials selected from the group consisting of natural and synthetic rubbers, polyurethanes, polyvinyl acetate, and polyvinyl chloride.

16. A method comprising utilizing the dispersion according to claim 1 for bonding porous or water vapor-permeable substrates by wet-in-wet processes.

Assignments (4)
CHANGE OF NAME Recorded Apr 7, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038374/0844 →
CHANGE OF NAME Recorded Mar 21, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038188/0408 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2016
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER MATERIALSCIENCE AG
Reel/Frame 038056/0732 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 29, 2014
From: KRAUS, HARALD; ARNDT, WOLFGANG; WINTERMANTEL, MATTHIAS
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 033637/0225 →
Priority Claims (1)
EP 11185228 · Oct 14, 2011 · regional
Continuity (1)
Related Publication 20140249267A1 · Sep 4, 2014