Adhesive composition

• US 5,508,111 A
• Filed: 03/05/1993
• Issued: 04/16/1996
• Est. Priority Date: 03/13/1991
• Status: Expired due to Term

• Current Assignee: Ashland Licensing and Intellectual Property Llc
• Original Assignee: Gencorp Incorporated
• Inventors: Schmucker, Arden E.
• Primary Examiner(s): Michl, Paul R.
• Assistant Examiner(s): NILAND, PATRICK DENNIS
• Application Number:
  US08/027,542
• Time in Patent Office: 1,138 Days
• Field of Search: 524/196, 524/198, 524/590, 524/871, 528/60, 528/61, 528/64, 428/423.1
• US Class Current: 428/423.1
• 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 18/3237 aromatic C08G18/3234 takes precedence
• CPC Class Codes: C08G 18/6618 with compounds of group C08G18/3225 or polyamines of C08G18/38
• CPC Class Codes: C08L 2666/54 Inorganic substances
• CPC Class Codes: C09J 175/12 from compounds containing nitrogen and active hydrogen, the nitrogen atom not being part of an isocyanate group
• CPC Class Codes: Y10T 428/31551 Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]

Abstract

A polyurethane adhesive formed from (I) an NCO terminated prepolymer with excess of NCO and talc, and (II) a polyol, a urethane catalyst, talc and a minor amount of certain aryl or aromatic polyamines exhibits good sag and thixotropic properties and, also, exhibits good lap shear strength when cured between treatment-free substrates.

Claims

1. In an adhesive composition comprising a polyurethane and polyurea resin system, a catalyst, optionally one or more fillers and optionally a pigment and/or dye,

wherein said resin system comprises a prepolymer and a curative composition, said prepolymer being a urethane prepolymer having terminal free --NCO groups, said curative composition comprising one or more polyamines and one or more polyols capable of forming a cross linked polyurethane,

the improvement wherein the isocyanate index (--NCO/(--OH+--NH)) of said resin system is from 1.20 to 2 and wherein said one or more polyamines consist essentially of one or more aromatic polyamines, said one or more aromatic polyamines being one or more primary aromatic polyamines with fused polycyclic aromatic rings having at least 2 NH₂ groups per molecule, and having H, NH₂, C₁ to C₅ alkyl, or phenyl groups attached to the ring carbons which are not bridge-head carbons.

2. The method which comprises applying between two treatment-free substrates selected from fiberglass reinforced plastic, metal, and plastic the composition of claim 1, then pressing and heating the substrates to cure said composition to adhesively join the two substrates.

3. A laminate comprising two substrates adhered together with the heat and pressure cured adhesive composition of claim 1.

4. The composition of claim 1 wherein said isocyanate index is between 1.35 to about 1.6.

5. The composition of claim 4 wherein said isocyanate index is between 1.35 to about 1.45.

6. The composition of claim 1 wherein said polyol of said curative is a propylene oxide adduct of pentaerythritol.

7. The composition of claim 1 wherein said polyamine is 1,8-diamino naphthalene.

12. The composition of claim 4 wherein said aromatic polyamines of said curative consist of 1,8-diamino naphthalene.

17. As an article of manufacture, a fiber reinforced plastic substrate adhesively bonded to an other substrate with the adhesive of claim 1, said plastic substrate and said other substrate being free of a surface primer for said adhesive.

18. The article of claim 17 wherein said one or more polyamines of said curative consists of 1,8-diamino napthalene.

19. The article of claim 18 wherein said other substrate is also a fiber reinforced plastic.

9. A laminate comprising two substrates adhered together with a heat cured adhesive, said adhesive prior to curing comprising a polyurethane and polyurea resin system, a catalyst, optionally one or more fillers and optionally a pigment and/or dye,

wherein said resin system comprises a prepolymer and a curative composition, said prepolymer being a urethane prepolymer having terminal free --NCO groups, said curative composition comprising one or more polyamines and one or more polyols capable of forming a cross linked polyurethane,

wherein the isocyanate index (--NCO/(--OH+--NH)) of said resin system is from 1.20 to 2 and wherein said one or more polyamines consist essentially of one or more aromatic polyamines, said one or more aromatic polyamines being

(a) one or more primary aromatic polyamines having the formula ##STR3## where R₁ is ##STR4## or the same as any of R₂ through R₆ and where the R₂ through R₆ and R₇ through R₁₁ are independently selected from the groups of:

H;

NH₂ ;

C₁ to C₅ alkyl;

or phenyl;

wherein A is an alkylene hydrocarbon containing 0 to 12 carbons and each molecule contains at least 2 NH₂ groups, when R₁ is not Formula II, at least 4 of the R₁ through R₆ groups are not H, and Formula I is not diethyl toluene diamine, and where R₁ is Formula II and A is 1 to 12 carbon atoms at least 4 of the R₂ through R₁₁ groups are not H or

(b) one or more primary aromatic polyamines with fused polycyclic aromatic rings having at least 2 NH₂ groups per molecule, and having H, NH₂, C₁ to C₅ alkyl, or phenyl groups attached to the ring carbons which are not bridge-head carbons or combinations thereof.

8. The composition of claim 14 wherein said composition has a thixotropic index of more than 3.

10. A laminate according to claim 9, wherein the adhesive prior to curing has a thixotropic ratio above 3 and an NCO:

(OH+NH) ratio of 1.35 to 1.6 and wherein at least one substrate is a fiber reinforced plastic substrate and the other substrate is a fiber reinforced plastic, metal, or other plastic substrate.

11. A laminate according to claim 10 wherein said one or more polyamines of said curative consist of said primary aromatic polyamines.

13. A laminate according to claim 10 wherein said polyamines are at least one amine set forth in group (a).

14. A laminate according to claim 10 wherein said polyamines are at least one amine set forth in group (b).

15. A laminate according to claim 10 wherein said one or more polyamines are at least one amine with said fused polycyclic aromatic rings.

16. A laminate according to claim 10 wherein said one or more polyamines are at least one member from the group consisting of (i) 2,3,5,6-tetramethyl-1,4-phenylene diamine (ii) 3,3'"'"'-dimethyl-4,4'"'"'-diaminobiphenyl (iii) 3,3'"'"',4,4'"'"'-tetraaminobiphenyl (iv) 4,4'"'"'-methylene bis(3-methylaniline) and (v) 4,4'"'"'-diamino-2,2'"'"'-dimethylbibenzyl.

20. In an adhesive composition comprising a polyurethane and polyurea resin system, a catalyst, optionally one or more fillers and optionally a pigment and/or dye, and wherein said resin system comprises a prepolymer and a curative composition, said prepolymer being a urethane prepolymer having terminal free --NCO groups, said curative composition comprising one or more primary polyamines and one or more polyols capable of forming a cross linked polyurethane,

the improvement wherein the isocyanate index of NCO groups to OH+NH₂ groups of said resin system is from 1.20 to 2 and wherein said one or more primary polyamines consist of one or more aromatic polyamines having an effective reactivity with the prepolymer to form a polyurethane having good sag resistance and good lap shear properties and being one or more primary aromatic polyamines with fused polycyclic aromatic rings having at least 2 NH₂ groups per molecule, and having H, NH₂, C₁ to C₅ alkyl, or phenyl groups attached to the ring carbons which are not bridge-head carbons.

21. The composition of claim 20 wherein said one or more polyamines is 1,5-diamino naphthalene or 1,8-diamino naphthalene, wherein the molecular weight of said one or more polyol curatives is from about 450 to about 600, and wherein said isocyanate index is between about 1.35 to about 1.6.

22. The composition of claim 21, wherein said polyisocyanate is MDI, wherein said composition has a thixotropic index of more than 5, and wherein said composition is cured above 90°

C.

23. The method which comprises applying between two primer-free substrates selected from fiberglass reinforced plastic, metal, and plastic the composition of claim 20, then pressing and heating to greater than 50°

C. the substrates to cure said composition to adhesively join the two substrates.

24. A laminate comprising two substrates adhered together with the heat and pressure cured adhesive composition of claim 20.

25. The composition of claim 20, wherein an effective amount of said one or more primary aromatic polyamines is used such that the thixotropic index is above 5 and the composition is cured by heating to greater than 90°

C.

26. The composition of claim 22, wherein the composition is free from primary,aliphatic polyamines, and wherein from about 0.5 to about 3 parts by wt. of said one or more primary aromatic polyamines is used/per 100 parts by wt. of said curative.

27. In an adhesive composition comprising a resin system, a catalyst, optionally one or more fillers and optionally a pigment and/or dye, and wherein said resin system comprises a prepolymer and a curative composition, said prepolymer being a urethane prepolymer formed by reacting a polyol with polyisocyanate in a equivalent ratio (NCO/OH) of about 2 to about 20 and said curative composition comprising a primary polyamine and a polyol and wherein the isocyanate index NCO/(OH+NH₂) of said resin system is about 1.20 to 2, the improvement wherein said composition is free of fast reacting primary aliphatic amines and wherein said polyamine of said curative is one or more primary aromatic polyamines with fused polycyclic aromatic rings having at least 2 NH₂ groups per molecule, and having H, NH₂, C₁ to C₅ alkyl, or phenyl groups attached to the ring carbons which are not bridge-head carbons.

28. The composition of claim 27, wherein said primary polyamines is 1,8 or 1,5-diamino naphthalene, wherein said polyisocyanate is MDI, and wherein the thixotropic index of the composition is more than 5.0.

29. The composition of claim 28, wherein said polyol of said curative has an average molecular weight from about 400 to about 650, wherein said composition is cured above 90°

C., and wherein said isocyanate index is between about 1.35 to about 1.6.

30. As an article of manufacture, a fiber reinforced plastic substrate adhesively bonded to another substrate with the adhesive of claim 27, said plastic substrate and said other substrate both being free of a surface primer for said adhesive.

31. As an article of manufacture, a fiber reinforced plastic substrate adhesively bonded to another substrate with the adhesive of claim 29, said plastic substrate and said other substrate both being free of a surface primer for said adhesive.

32. The article of claim 31, wherein said other substrate is also a fiber reinforced plastic.

33. A process for adhesively joining two or more substrates individually selected from fiberglass reinforced plastic, metal, and plastic free of a surface primer, the process comprising;

mixing a urethane prepolymer having unreacted isocyanate terminal groups with a curative component forming a urethane adhesive, wherein said curative component comprises one or more polyols and one or more polyamines having primary amine groups;

wherein all said primary amines consist essentially of aromatic primary amines;

applying said urethane adhesive to the two or more substrates;

thickening said urethane adhesive by forming homogeneously dispersed urea linkages from the isocyanate terminal groups and said one or more aromatic primary polyamines; and

heating said urethane adhesive to a temperature above 50°

C. to cure said urethane adhesive and bond said two or more substrates;

said one or more primary polyamines being used in amounts from 0.5 to 3 parts by wt. per 100 parts by wt. of said curative component and they consist essentially of

(a) one or more primary aromatic polyamines having the formula ##STR5## where R₁ is ##STR6## or the same as any of R₂ through R₆ and where the R₂ through R₆ and R₇ through R₁₁ are independently selected from the groups of;

H;

NH₂ ;

C₁ to C₅ alkyl;

or phenyl, A is an alkylene hydrocarbon containing 0 to 12 carbons and each molecule contains at least 2 NH₂ groups, where R₁ is not Formula II, at least 4 of the R₁ through R₆ groups are not H, and Formula I is not diethyl toluene diamine, and where R₁ is Formula II and A is 1 at least 4 of the R₂ through R₁₁ groups are not H, or

(b) one or more primary aromatic polyamines with fused polycyclic aromatic rings having at least 2 NH₂ groups per molecule, and having H, NH₂, C₁ to C₅ alkyl, or phenyl groups attached to the ring carbons which are not bridge-head carbons, or combinations thereof, and wherein said thickening occurs in 3 seconds or less after said mixing process.

34. A process according to claim 33, wherein said one or more polyamines is 1,5-diamino naphthalene or 1,8-diamino naphthalene, wherein the molecular weight of said one or more polyol curatives is from about 450 to about 600, and wherein said isocyanate index is between about 1.35 to about 1.6.

35. A process according to claim 33, wherein said polyisocyanate is MDI, wherein said composition has a thixotropic index of more than 5, and wherein said composition is cured above 90°

C.