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Disclosed are epoxy resins exhibiting a highly favorable combination of tensile strength and elongation with respect to prior art epoxy systems. The elastomeric epoxy resin systems of the invention are prepared utilizing a curing agent containing at least one monoprimary amine, and are particularly

Disclosed are epoxy resins exhibiting a highly favorable combination of tensile strength and elongation with respect to prior art epoxy systems. The elastomeric epoxy resin systems of the invention are prepared utilizing a curing agent containing at least one monoprimary amine, and are particularly useful in applications such as, for example, castings, potting, composites, crack sealing, coatings, adhesives, roofing materials, flooring or reinforced membranes.

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1. A composition comprising an epoxy resin system, the epoxy resin system comprising a reaction product of: an epoxy resin component;a curing agent comprising a monoprimary amine represented by the formula R—NH2 wherein R is a hydrocarbyl group containing between about 8 and about 50 carbon atoms; a

1. A composition comprising an epoxy resin system, the epoxy resin system comprising a reaction product of: an epoxy resin component;a curing agent comprising a monoprimary amine represented by the formula R—NH2 wherein R is a hydrocarbyl group containing between about 8 and about 50 carbon atoms; andan accelerator selected from the group consisting of sulfonates, phosphonates, sulfates, tetrafluoroborates, carboxylates and nitrates of Groups IA, IIA and transition metals of the Periodic Table (CAS version); inorganic acids, carboxylic acids, phenolic compounds, imidazoles, cyanamide, sulfonamides, and imides;wherein the curing agent is substantially free of a crosslinking agent having at least 3 active hydrogen atoms; andwherein, when cured, the reaction product exhibits a tensile strength of >1 MPa and an elongation of >100% as measured by ASTM D-638 at 25° C., wherein the composition is free of asphalt. 2. The composition of claim 1 wherein the curing agent further comprises an amine terminated polyamide which is the reaction product of a dimerized fatty acid or hydrogenated dimerized fatty acid with an amine containing one primary and one secondary amine group or two secondary amine groups. 3. The composition of claim 2 wherein the amine terminated polyamide is prepared by reacting: (a) carboxylic acids selected from C18-C60 dicarboxylic acids, C18-C60 dicarboxylic acid derivatives and mixtures thereof, wherein the carboxylic acids optionally contain di- or polycarboxylic acids or acid derivatives having from 4 to 20 carbon atoms in an amount ranging from 0-10% based on all carboxylic acids; and(b) at least one amine having the formula: R1—NH—R2—NH—R3 wherein R1 has a total number of carbon atoms from 0 to about 20 and is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, arylalkyl, hydroxyalkyl, alkoxyalkyl, cyanoalkyl, alkylthioalkyl, dialkylaminoalkyl, aryl, alkylaryl, cyanoaryl, alkoxyaryl, alkylthioaryl, and dialkylaminoaryl; R3 has a total number of carbon atoms from 1 to about 20 and is selected from the group consisting of alkyl, cycloalkyl, alkenyl, arylalkyl, hydroxyalkyl, alkoxyalkyl, cyanoalkyl, alkylthioalkyl, dialkylaminoalkyl, aryl, alkylaryl, cyanoaryl, alkoxyaryl, alkylthioaryl, and dialkylaminoaryl; andR2 is (CR4R5)n, wherein n is from 2 to about 20, R4 is independently selected for each (CR4R5) from the group consisting of H, alkyl, aryl, hydroxyl, alkoxy, alkylthio, dialkylamino and cyano; and R5 is independently selected for each (CR4R5) from the group consisting of H, alkyl and aryl. 4. The composition of claim 2 wherein the amine terminated polyamide is prepared by reacting: at least one C18-C50 dicarboxylic acid, dicarboxylic acid ester or dicarboxylic acid chloride with an aminoalkylpiperazine having the formula: wherein R1 is hydrogen and R2 is —R3—NH2 wherein R3 is a divalent aliphatic linkage with optional —CHR4 and —CR4R5 units, wherein R4 and R5 are independently alkyl groups. 5. The composition of claim 1 wherein the epoxy resin system further comprises a monofunctional or polyfunctional epoxy diluent. 6. The composition of claim 1 wherein the epoxy resin system further comprises a polyacrylate ester of a polyol or polymethacrylate ester of a polyol. 7. The composition of claim 1 wherein the epoxy resin system further comprises one or more amine-containing curing agents comprising a primary amine moiety or two or more primary or secondary amine or amide moieties linked to a common central organic moiety. 8. The composition of claim 1 wherein the monoprimary amine comprises one or more primary fatty amines selected from the group consisting of octylamines, laurylamines, myristylamines, palmitylamines, stearylamines, oleylamine, tallowamines, hydrogenated tallow amines, cetylamines, N-tetradecylamine, cocoamines, soyamines, and combinations thereof. 9. The composition of claim 1 wherein the curing agent has a Brookfield viscosity of 3000 cP or less at 25° C. 10. The composition of claim 1 wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a Tg below 30° C. as measured by Differential Scanning Calorimetry. 11. A composition comprising a curable epoxy resin system, the curable epoxy resin system comprising a reaction product of: an epoxy resin component;a curing agent consisting essentially of a monoprimary amine represented by the formula R—NH2 wherein R is a hydrocarbyl group containing between about 8 and about 50 carbon atoms; andan accelerator selected from the group consisting of sulfonates, phosphonates, sulfates, tetrafluoroborates, carboxylates and nitrates of Groups IA, IIA and transition metals of the Periodic Table (CAS version); inorganic acids, carboxylic acids, phenolic compounds, imidazoles, cyanamide, sulfonamides, and imides:wherein the curing agent is substantially free of a crosslinking agent having at least 3 active hydrogen atoms;wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a tensile strength of >1 MPa and an elongation of >100% as measured by ASTM D-638 at 25° C, wherein the composition is free of asphalt. 12. A composition comprising an epoxy resin system, the epoxy resin system comprising a reaction product of: an epoxy resin component;a curing agent comprising greater that 70 wt % of a monoprimary amine represented by the formula R—NH2 wherein R is a hydrocarbyl group containing between about 8 and about 50 carbon atoms; andan accelerator selected from the group consisting of sulfonates, phosphonates, sulfates, tetrafluoroborates, carboxylates and nitrates of Groups IA, HA and transition metals of the Periodic Table (CAS version); inorganic acids, carboxylic acids, phenolic compounds, imidazoles, cyanamide, sulfonamides, and imides;wherein the curing agent is substantially free of a crosslinking agent having at least 3 active hydrogen atoms;wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a tensile strength of >1 MPa and an elongation of >100% as measured by ASTM D-638 at 25° C, wherein the composition is free of asphalt. 13. The composition of claim 12 wherein the curing agent further comprises an amine terminated polyamide which is the reaction product of a dimerized fatty acid or hydrogenated dimerized fatty acid with an amine containing one primary and one secondary amine group or two secondary amine groups. 14. The composition of claim 11 wherein the curing agent has a Brookfield viscosity of 3000 cP or less at 25° C. 15. The composition of claim 11 wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a Tg below 30° C. as measured by Differential Scanning Calorimetry. 16. The composition of claim 12 wherein the curing agent has a Brookfield viscosity of 3000 cP or less at 25° C. 17. The composition of claim 12 wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a Tg below 30° C. as measured by Differential Scanning Calorimetry. 18. A composition comprising an epoxy resin system, the epoxy resin system comprising a reaction product of: an epoxy resin component;a curing agent comprising less than 20 wt % of a monoprimary amine represented by the formula R—NH2 wherein R is a hydrocarbyl group containing between about 8 and about 50 carbon atoms; andan accelerator selected from the group consisting of sulfonates, phosphonates, sulfates, tetrafluoroborates, carboxylates and nitrates of Groups IA, IIA and transition metals of the Periodic Table (CAS version); inorganic acids, carboxylic acids, phenolic compounds, imidazoles, cyanamide, sulfonamides, and imides;wherein the curing agent is substantially free of a crosslinking agent having at least 3 active hydrogen atoms;wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a tensile strength of >1 MPa and an elongation of >100% as measured by ASTM D-638 at 25° C, wherein the composition is free of asphalt. 19. The composition of claim 18 wherein the curing agent has a Brookfield viscosity of 3000 cP or less at 25° C. 20. The composition of claim 18 wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a Tg below 30° C. as measured by Differential Scanning Calorimetry. 21. The composition of claim 7 wherein the one or more amine-containing curing agents comprise a diamine. 22. The composition of claim 7 wherein the one or more amine-containing curing agents comprise an aliphatic diamine, a polyoxypropylene diamine, and a cycloaliphatic diamine. 23. The composition of claim 1, wherein the accelerator is selected from the group consisting of alkylbenzenesulfonates, HBF4, H2SO4, H2NSO3H, and H3PO4, salicylic acid, lactic acid, glycolic acid, resorcylic acid, phenol, t-butylphenol, nonylphenol, bisphenol A, dicyandiamide, cyanamide, p-toluenesulfonamide, phthalimide, succinimide, maleimide, perylenetetracarboxylic diimide, saccharin, calcium nitrate, calcium alkylbenzene sulfonates, magnesium alkanesulfonates, tetrafluoroboric acid, dichloroacetic acid, trifluoroacetic acid, thiocyanic acid and mercaptoacetic acid.