Low monomer polyurethane prepolymer and process therefore

• US 6,515,164 B1
• Filed: 07/02/1999
• Issued: 02/04/2003
• Est. Priority Date: 01/02/1997
• Status: Expired due to Term

• Current Assignee: Henkel KGaA (Henkel AG & Co KGaA)
• Original Assignee: Henkel KGaA (Henkel AG & Co KGaA)
• Inventors: Omoruyi, Astrid, Bolte, Gerd, Henke, Guenter, Kruedenscheidt, Markus
• Primary Examiner(s): SERGENT, RABON A
• Application Number:
  US09/341,080
• Time in Patent Office: 1,313 Days
• Field of Search: 252/182.2, 252/182.21, 252/182.22, 528/59, 528/60, 528/61, 528/65, 528/66, 528/67, 528/76, 528/80, 528/85, 560/25, 560/26, 560/115, 560/330, 560/158, 560/336, 560/358, 560/359, 560/360, 156/331.4, 156/331.7
• US Class Current: 560/25
• CPC Class Codes: B32B 7/12 using interposed adhesives or interposed materials with bonding properties
• CPC Class Codes: C08G 18/10 Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
• CPC Class Codes: C08G 18/721 Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
• CPC Class Codes: C08G 18/7607 Compounds of C08G18/7614 and of C08G18/7657
• CPC Class Codes: C08G 18/7621 being toluene diisocyanate including isomer mixtures
• CPC Class Codes: C08G 18/7671 containing only one alkylene bisphenyl group
• CPC Class Codes: C09J 175/04 Polyurethanes

Abstract

A low-monomer PU prepolymer containing free NCO groups which is obtained from polyhydric alcohols and diisocyanates differing in their reactivity and which is distinguished by the ratio of the NCO groups of the partly slower-reacting diisocyanate to the NCO groups of the faster-reacting diisocyanate. It is greater than 6:1. Nevertheless the prepolymer according to the invention cures more quickly than a known prepolymer predominantly containing fast-reacting NCO groups. In a preferred embodiment, TDI is used as the partly slower-reacting diisocyanate while MDI is used as the faster-reacting diisocyanate. The prepolymer is produced in two stages. The prepolymer according to the invention is suitable for bonding plastic articles, metals and paper, especially films. The accelerated absence of migration is particularly noticeable in this regard.

Claims

1. A low-monomer polyurethane prepolymer containing free isocyanate groups obtained by reacting one or more polyhydric alcohols and two or more diisocyanates, wherein the polyhydric alcohol is first reacted with at least one non-symmetrical diisocyanate having a first NCO group which has a slower rate of reaction with the polyhydric alcohol than a second NCO group, wherein a ratio of a number of OH groups to a number of first and second NCO groups is form 4:

1 to 0.55;

1, to form a reaction product having free OH groups and free first NCO groups, and reacting the reaction product with at least one second diisocyanate having NCO groups which have a faster rate of reaction with the polyhydric alcohol than the first NCO groups wherein a ratio of a total number of first and second NCO groups of the non-symmetrical diisocyanate to a number of NCO groups of the second diisocyanate is greater than 6;

1 and the second diisocyanate is added in an amount less than an equivalent of free OH groups in the reaction product.

2. The low-monomer polyurethane prepolymer of claim 1 wherein said ratio of the total number of first and second NCO groups to the number of NCO groups of the second diisocyanate is greater than 10:

1.

3. The low-monomer polyurethane prepolymer of claim 1 wherein said polyhydric alcohols are selected from the group consisting of primary and secondary aliphatic alcohols containing 2 to 6 hydroxyl groups.

4. The low-monomer polyurethane prepolymer of claim 1 wherein the at least one second diisocyanate having NCO groups which have a faster rate of reaction than the first NCO groups comprise a symmetrical aromatic diisocyanate.

5. The low-monomer polyurethane prepolymer of claim 1 containing free isocyanate groups obtained by reacting one or more polyhydric alcohols selected from the group consisting of primary and secondary aliphatic alcohols containing 2 to 6 hydroxyl groups and two or more diisocyanates, wherein, the at least one second diisocyanate having the NCO group with a faster rate of reaction than the first NCO group comprises a symmetrical aromatic diisocyanate and the ratio of the NCO groups of the non-symmetrical diisocyanate to the NCO groups of the symmetrical aromatic diisocyanate is greater than 10:

1.

6. The low-monomer polyurethane prepolymer of claim 5 wherein the ratio of the NCO groups of the non-symmetrical diisocyanate to the NCO groups of the symmetrical aromatic diisocyanate is greater than 15.1.

7. The low-monomer polyurethane prepolymer of claim 5 wherein the polyhydric alcohols are selected from the group consisting of diols containing 2 to 5 carbon atoms, triols containing 3 to 6 carbon atoms, tetraols containing 4 to 8 carbon atoms, OH-functional esters having molecular weights up to 10,000, OH-functional polyethers having molecular weights up to 10,000, and mixtures thereof.

8. The low-monomer polyurethane prepolymer of claim 5 wherein the symmetrical aromatic diisocyanate comprises 4,4′

MDI.

9. The low-monomer polyurethane prepolymer of claim 5 wherein the non-symmetrical diisocyanate comprises TDI.

15. A method of bonding two substrates selected from the group consisting of plastic surface articles, metals and paper comprising:

applying the prepolymer of claim 1 alone or in a mixture with a hardener to at least one surface of the substrates to be joined;

bringing the surfaces of the substrates to be joined together with the prepolymer therebetween; and

curing the prepolymer with a hardener, moisture or both to form an adhesive bond between the substrates.

16. The method of claim 15 wherein at least one of the substrates is a film.

17. The method of claim 15 wherein said curing is carried out at a temperature between 20°

C. and 120°

C.

18. The method of claim 15 wherein the hardener contains at least one functional group selected from the group consisting of amino groups, carboxylic acid groups, alcohol groups and epoxide groups.

10. A process for producing a low-monomer polyurethane prepolymer containing free isocyanate groups comprising the steps of:

(a) reacting one or more non-symmetrical diisocyanates, each containing a first NCO group which has a slower rate of reaction than a second NCO group, with one or more polyhydric alcohols in an OH;

NCO ratio of 4;

1 to 0.55;

1 until at least substantially all of the second NCO groups, but substantially none of the first NCO groups, have reacted with the OH groups of the polyhydric alcohols to form a reaction product having free OH groups and free first NCO groups;

(b) reacting the reaction product of step (a) with at least one symmetrical diisocyanate, each containing NCO groups which have a faster rate of reaction than the first NCO groups of the non-symmetrical diisocyanates, to form the low-monomer polyurethane prepolymer, wherein said symmetrical diisocyanates are added in an amount less than equivalents of free OH groups present in said reaction product of step (a) and a ratio of a total number of first and second NCO groups of the non-symmetrical diisocyanate to a number of NCO groups of the symmetrical diisocyanate is greater than 6;

1.

11. The process of claim 10 wherein steps (a) and (b) are carried out at temperatures of 40°

C. to 120°

C.

12. The process of claim 10 wherein TDI comprises at least one of the non-symmetrical diisocyanates in step (a).

13. The process of claim 10 wherein 4,4′

MDI comprises the at least one symmetrical diisocyanates in step (b).

14. The process of claim 10 wherein the OH:

NCO ratio in step (a) is between 1;

1 and 0.6;

1.