Epoxy resins adducted with reactive liquid rubber having improved low temperature performance properties

1. A one part blend of uncured epoxy resins, comprising:

a reaction product of one or more epoxy resins with one or more carboxyl terminated polybutadienes (CTB) and with one or more carboxyl terminated poly(butadiene-acrylonitrile)s (CTBN) or with one or more random pendant and terminal carboxyl functional poly(butadiene acrylonitrile)s (CTBNX) or with both said CTBN and said CTBNX, with the proviso, that the weight ratio of said CTBN or said CTBNX or both said CTBN and said CTBNX to said CTB is from about 1.0 to about 3.0, wherein said CTBN and said CTBNX have a nitrile content, independently, of from about 20% to about 40% by weight, and wherein the stoichiometric equivalence of the total amount of said epoxy resins to the total stoichiometric equivalence of said CTB, and said CTBN and said CTBNX is from about 2.0 to about 2.5,

an amount of unreacted epoxy resin so that the total amount of said CTB and said CTBN and said CTBNX is from about 5 parts to about 40 parts by weight per 100 total parts by weight of said reacted and said unreacted epoxy resin;

wherein said blend of said reacted product and said unreacted epoxy resin contains less than about 0.25 parts by weight of a catalyst per 100 total parts by weight of the total amount of all epoxies, CTB, CTBN, and/or CTBNX components;

wherein said blend contains less than 40 parts by weight of one or more inorganic fillers per 100 total parts by weight of said reacted epoxy-CTB-CTBN and/or epoxy-CTB-CTBNX resin; and

wherein said blend of said uncured reacted product and said unreacted epoxy resin are miscible upon storage.

2. The blend of epoxy resins according to claim 1 , wherein said one or more epoxy resins and said unreacted epoxy resin, independently, comprises a glycidyl or diglycidyl ether of novolac resin; glycidyl ether of di-, and trihydric phenol; glycidyl or diglycidyl ether of bisphenol; glycidyl ether of polynuclear phenol; epoxy resin made from diphenolic acid; glycidyl ether of aliphatic polyol: glycidyl ester; glycidyl epoxy containing nitrogen; glycidyl derivative of cyanuric acid; glycidyl resin from melamine; glycidyl amine; glycidyl triazine; thioglycidyl resin; silicon-glycidyl resin; fluorine glycidyl resin; and epoxy resin synthesized from a polyglycidyl compound containing unsaturation; or a diglycidyl ether or a polyglycidyl ether in lieu of any of said above glycidyl ethers; or any combination thereof,

wherein said CTB optionally contains from about 0.1% to about 12% by weight of a nitrile; wherein the number average molecular weight of said CTB is from about 2,000 to about 8,000, wherein the number average molecular weight of said CTBN is from about 2,000 to about 8,000, and wherein the number average molecular weight of said CTBNX compound is from about 2,000 to about 8,000.

3. The blend of epoxy resins according to claim 2 , wherein the nitrile content of said CTBN is from about 20% to about 35% by weight based upon the total weight of said CTBN compound, wherein the nitrile content of said CTBNX is from about 20% to about 35% by weight based upon the total weight of said CTBN compound, and wherein said B of said CTB compound is butadiene.

4. The blend of epoxy resins according to claim 3 , wherein said epoxy resin is the diglycidyl ether of bisphenol A; wherein the weight ratio of said CTBN or said CTBNX or both said CTBN and CTBNX to said CTB is from about 1 to about 2; wherein said B of said CTBN is derived from butadiene, wherein said B of said CTBNX is derived from butadiene; wherein the stoichiometric equivalence of the total amount of said reacted epoxy resins to the total stoichiometric equivalence of said CTB and said CTBN and said CTBNX is from about 2.0 to about 2.3, and wherein the amount of said filler is less than 20 parts by weight.

5. The blend of epoxy resins according to claim 4 , wherein said CTB is miscible with said unreacted epoxy resin for at least three months.

6. A cured composition of claim 4 , including a curing agent that is an amine compound, wherein said cured composition has a peel strength at minus 40° C. according to ASTM D-1876 of from about 6 to about 10 Newtons per millimeter

7. The blend of epoxy resins according to claim 4 , wherein the nitrile content of said CTBN is from about 21% to 32% by weight, wherein the nitrile content of said CTBNX is from about 21% to about 32% by weight, wherein the number average molecular weight of said CTB is from about 3,000 to about 4,500, wherein the number average molecular weight of said CTBN is from about 3,000 to about 4,500, wherein the number average molecular weight of said CTBNX is from about 3,000 to about 4,500; and wherein the total amount of said CTB and said CTBN and said CTBNX, is from about 10 parts to about 30 parts by weight per 100 total parts by weight of said reacted and unreacted epoxy resin.

8. The blend of epoxy resins according to claim 7 , wherein said CTB is miscible with said unreacted epoxy resin for at least six months.

9. A cured composition of claim 8 , including a curing agent that is dicyandiamide, and wherein said cured composition has a peel strength at minus 40° C. according to ASTM D-1876 of from about 7 to about 10 Newtons per millimeter.

10. The blend of epoxy resins according to claim 1 , wherein said CTB is miscible with said unreacted epoxy resin.

11. A cured composition of claim 10 , including a curing agent that is an amine compound comprising a primary, secondary, or a tertiary amine having a total of from 2 to about 42 carbon atoms, or a urea, or a substituted urea compound, or any combination thereof, wherein said cured composition has a peel strength at minus 40° C. according to ASTM D-1876 of from about 6 to about 10 Newtons per millimeter.

12. A cured composition of claim 1 , wherein said cured composition has a peel strength at minus 40° C. according to ASTM D-1876 of from about 5 to about 10 Newtons per millimeter.

13. A process for making a one part blend of uncured epoxy resins containing a carboxyl terminated polybutadiene (CTB) rubber adducted epoxy resin comprising the steps of:

reacting one or more epoxy resins with one or more of said CTB and with one or more carboxyl terminated poly(butadiene-acrylonitrile)s (CTBN), or with one or more random pendant and terminalcarboxyl functional poly(butadiene acrylonitrile)s (CTBNX) or with both said CTBN and said CTBNX, with the proviso that the weight ratio of said CTBN or said CTBNX or both said CTBN and said CTBNX to said CTB is from about 1.0 to about 3.0, wherein said CTB optionally contains a nitrile content of from about 0.1% to about 12% by weight, wherein said CTBN and said CTBNX have a nitrile content, independently, of from about 20% to about 40% by weight, and wherein the stoichiometric equivalence of the total amount of said epoxy resin to the total stoichiometric equivalence of said CTB, and said CTBN and said CTBNX is from about 2.0 to about 2.5,

subsequently blending said reacted epoxy resin with an amount of unreacted epoxy resin so that the total amount of said CTB and said CTBN and said CTBNX is from about 5 parts to about 40 parts by weight per 100 total parts by weight of said reacted and said unreacted epoxy resin;

said blend of said reaction product and said unreacted epoxy resin containing about 0.25 parts by weight or less of a catalyst per 100 parts by weight of the total amount of said one or more epoxies, said CTB, said CTBN, and/or said CTBNX components;

wherein said blend contains less than 40 parts by weight of one or more inorganic fillers per 100 total parts by weight of said reacted epoxy-CTB-CTBN and/or epoxy-CTB-CTBNX resin; and

wherein upon aging said blend of said uncured reaction product and said unreacted epoxy resin are miscible.

14. The process of claim 13 , wherein said one or more epoxy resins and said unreacted epoxy resins, independently, comprises a glycidyl or diglycidyl ether of novolac resin; glycidyl ether of di-, and trihydric phenol; glycidyl or diglycidyl ether of bisphenol; glycidyl ether of polynuclear phenol; epoxy resin made from diphenolic acid; glycidyl ether of aliphatic polyol: glycidyl ester; glycidyl epoxy containing nitrogen; glycidyl derivative of cyanuric acid; glycidyl resin from melamine; glycidyl amine; glycidyl triazine; thioglycidyl resin; silicon-glycidyl resin; fluorine glycidyl resin; and epoxy resin synthesized from a polyglycidyl compound containing unsaturation; or a diglycidyl ether or a polyglycidyl ether in lieu of any of said glycidyl ethers; or any combination thereof,

wherein the number average molecular weight of said CTB is from about 2,000 to about 8,000, wherein the number average molecular weight of said CTBN is from about 2,000 to about 8,000, and wherein the number average molecular weight of said CTBNX compound is from about 2,000 to about 8,000, and

wherein the nitrile content of said CTBN is from about 20% to about 35% by weight based upon the total weight of said CTBN compound, wherein the nitrile content of said CTBNX is from about 20% to about 35% by weight based upon the total weight of said CTBN compound, and wherein said B of said CTB compound is butadiene.

15. The process of claim 14 , wherein said epoxy resin is the diglycidyl ether of bisphenol A; wherein the weight ratio of said CTBN or CTBNX or both said CTBN and said CTBNX to said CTB is from about 1 to about 2; wherein said B of said CTBN is derived from butadiene, wherein said B of said CTBNX is derived from butadiene; and wherein said stoichiometric equivalence of the total amount of said reacted epoxy resins to the total stoichiometric equivalence of said CTB, and said CTBN and said CTBNX is from about 2.0 to about 2.3, and

wherein the nitrile content of said CTBN is from about 21% to 32% by weight, wherein the nitrile content of said CTBNX is from about 21% to about 32% by weight, wherein the number average molecular weight of said CTB is from about 3,000 to about 4,500, wherein the number average molecular weight of said CTBN is from about 3,000 to about 4,500, wherein the number average molecular weight of said CTBNX is from about 3,000 to about 4,500; and wherein the total amount of said CTB and said CTBN and said CTBNX is from about 10 parts to about 30 parts by weight per 100 total parts by weight of said reacted and unreacted epoxy resin,

and wherein the amount of said filler is less than 20 parts by weight.

16. The process of claim 15 , wherein upon aging for at least three months said blend of said reactive epoxy resin and said unreacted epoxy resin are miscible.

17. The process of claim 14 , including a curing agent, curing said blend of said reactive epoxy resin and said unreacted epoxy resin, wherein said curing agent comprises a primary, secondary, or a tertiary amine having a total of from 2 to about 42 carbon atoms, or a urea, or a substituted urea compound, or any combination thereof, and wherein said cured blend has a minus 40° C. ASTM D-1876 Peel strength of at least 7.0 Newtons per millimeter.

18. The process of claim 13 , wherein upon aging for at least three months said blend of said reactive epoxy resin and said unreacted epoxy resin are miscible.

19. The process of claim 18 , including a curing agent, curing said aged adhesive formulation containing the blend of said reactive epoxy resin and said unreacted epoxy resin, wherein said curing agent is dicyandiamide, and wherein said cured blend has a minus 40° C. ASTM D-1876 Peel strength of at least 8.0 Newtons per millimeter.

20. The process of claim 13 , including curing said blend of said reactive epoxy resin and said unreacted epoxy resin, and wherein said cured blend has a minus 40° C. ASTM D-1876 Peel strength of at least 6.0 Newtons per millimeter.