Epoxy Resin Adhesives

Abstract

A curable epoxy resin adhesive including first and second amine curing agents each having a respective curing property determined by mixing the respective amine curing agent alone with a test epoxy resin to form a first or second curable mixture, and each curing property comprises a gel time when the curable mixture is at an ambient temperature of 25° C. and a peak exotherm temperature when the curable mixture is cured in air at a curing temperature of 70° C. A ratio between the first and second gel times is from 4-15:1 and the second amine curing agent has peak exotherm temperature is higher than the peak exotherm temperature of the first amine curing agent by a temperature Δt which is at least 2° C.

Claims

1. A curable epoxy resin adhesive, the adhesive comprising an epoxy resin component and a curing agent component, wherein the epoxy resin component and the curing agent component are in a separated form and providing a mixture of the epoxy resin component and the curing agent component at a curing temperature of the adhesive causes curing of the epoxy resin component by the curing agent component, wherein the epoxy resin component comprises at least one epoxide-containing resin, and wherein the curing agent component comprises: (i) a first amine curing agent, wherein the first amine curing agent has a first curing property determined by mixing the first amine curing agent alone with a test epoxy resin to form a first curable mixture, wherein the test epoxy resin is one epoxide-containing resin of the epoxy resin component that is present in a concentration of more than 50 wt % of the at least one epoxide-containing resin, wherein the first curing property comprises (a1) a first gel time G1 when a 150 g sample of the first curable mixture is at an ambient temperature of 25° C. and (b1) a first peak exotherm temperature T1 when a 10 mL sample of the first curable mixture is cured in air at a curing temperature of 70° C.; and (ii) a second amine curing agent having the formula NH.sub.2—R—NH.sub.2 where R is any aliphatic or cycloaliphatic constituent, which is either unsubstituted or substituted with at least one functional group, or where R is any aromatic constituent, which is either unsubstituted or substituted with at least one functional group, wherein the curing agent component comprises from 15 to 60 wt % of the first amine curing agent and from 40 to 85 wt % of the second amine curing agent, each based on the total weight of the first and second amine curing agents, wherein the second curing agent has a second curing property determined by mixing the second amine curing agent alone with the test epoxy resin to form a second curable mixture, the second curing property comprising (a2) a second gel time G2 when a 150 g sample of the second curable mixture is at an ambient temperature of 25° C. and (b2) a second peak exotherm temperature T2 when a 10 mL sample of the second curable mixture is cured in air at a curing temperature of 70° C., wherein a ratio G2:G1 between the second and first gel times is from 4-15:1 and the second peak exotherm temperature T2 is higher than the first peak exotherm temperature T1 by a temperature Δt, wherein Δt is at least 2° C.

2. A curable epoxy resin adhesive according to claim 1 wherein the ratio G2:G1 between the second and first gel times is from 6:1-10:1.

3. A curable epoxy resin adhesive according to claim 1 wherein the first gel time G1 is from 15 to 35 minutes and the second gel time G2 is from 100 to 300 minutes.

4. A curable epoxy resin adhesive according to claim 3 wherein the first gel time G1 is from 20 to 30 minutes and the second gel time G2 is from 150 to 250 minutes.

5. A curable epoxy resin adhesive according to claim 1 wherein the first curing property further comprises (c1) a first time period P1 from initiation of curing to peak exotherm temperature and the second curing property further comprises (c2) a second time period P1 from initiation of curing to peak exotherm temperature, wherein P2 is greater than P1 by a time period ΔP of at least 100 seconds measured when the curing is carried out in air at a curing temperature of 70° C. and on a test resin sample having a volume of 10 mL.

6. A curable epoxy resin adhesive according to claim 5 wherein the time period ΔP is from 150 to 425 seconds, from 150 to 410 seconds, further optionally from 250 to 410 seconds.

7. A curable epoxy resin adhesive according to claim 1 wherein Δt is from 2 to 30° C. or from 2 to 25° C.

8. A curable epoxy resin adhesive according to claim 1 wherein the first peak exotherm temperature T1 is within the range of from 220 to 240° C. and/or the second peak exotherm temperature T2 is within the range of from 235 to 270° C.

9. A curable epoxy resin adhesive according to claim 8 wherein the first peak exotherm temperature T1 is within the range of from 230 to 240° C. and/or the second peak exotherm temperature T2 is within the range of from 237 to 265° C.

10. A curable epoxy resin adhesive according to claim 1 wherein the first amine curing agent has a first amine functionality corresponding to an active hydrogen equivalent weight (AHEW) of from 42-54 and the second amine curing agent has a second amine functionality which corresponds to an active hydrogen equivalent weight (AHEW) of from 15-40.

11. A curable epoxy resin adhesive according to claim 1 wherein the second amine curing agent comprises a linear, asymmetrically branched or cyclic aliphatic diamine or triamine.

12. A curable epoxy resin adhesive according to claim 1 wherein the second amine curing agent comprises 2-methylpentane-1,5-diamine, octane-1,8-diamine, cyclohexane-1,2-diamine, N.sup.1-(3-aminoethyl)ethane-1,2-diamine, N.sup.1-(3-aminopropyl)propane-1,3-diamine, 2,2,-(diaminoethyl) propane-1,2-diamine, 2,2,-dimethyl propane-1,3-diamine, octamethylenediamine, ethylenediamine, 1,3-diaminopropane, 1,2-prollenediamine, diethylenetriamine, dipropylene triamine, N,N-Bis-(3-amineopropyl)methylamine, 1,2-cyclohexane diamine, or any mixture of one or more thereof.

13. A curable epoxy resin adhesive according to claim 1 wherein the second amine curing agent comprises di(aminoalkyl) benzene, wherein each alkyl group has from 1 to 3 carbon atoms and the alkyl groups are the same or different in each aminoalkyl functional group.

14. A curable epoxy resin adhesive according to claim 1 wherein the second amine curing agent comprises xylylenediamine, such as 1,3-Bis(aminomethyl)benzene (m-xylylenediamine) or 1,4-Bis(aminomethyl)benzene (p-xylylenediamine), 1,3-Bis(aminoethyl)benzene, 1,4-Bis(aminoethyl)benzene, 1,3-Bis(aminopropyl)benzene or 1,4-Bis(aminopropyl)benzene, or any mixture of one or more thereof.

15. A curable epoxy resin adhesive according to claim 1 wherein the first amine curing agent comprises or consists of a modified or adducted triethylene tetramine.

16. A curable epoxy resin adhesive according to claim 15 wherein the curing agent component comprises or consists of a modified or adducted triethylene tetramine as the first amine curing agent and cyclohexane-1,2-diamine or 1,3-Bis(aminomethyl)benzene (m-xylylenediamine) as the second amine curing agent.

17. A curable epoxy resin adhesive according to claim 1 wherein the curing agent component comprises from 20 to 50 wt % of the first amine curing agent and from 50 to 80 wt % of the second amine curing agent, each based on the total weight of the first and second curing agents.

18. A curable epoxy resin adhesive according to claim 1 wherein the first curing property further comprises (c1) a glass transition temperature Tg2 of the cured epoxy resin which is within the range of from 94 to 98° C. after a curing time period of 5 hours at a curing temperature of 70° C. in air and the second curing property further comprises (c2) a glass transition temperature Tg2 of the cured epoxy resin which is within the range of from 87 to 93° C. after a curing time period of 5 hours at a curing temperature of 70° C. in air.

19. A curable epoxy resin adhesive according to claim 1 wherein the curing agent component has a third curing property determined by mixing the curing agent component with the test epoxy resin to form a third curable mixture, the third curing property comprising (a3) a gel time G3 of from greater than 28 minutes to up to 90 minutes when a 150 g sample of the third curable mixture is at an ambient temperature of 25° C., wherein the gel time G3 is between gel times G1 and G2, and (b3) a peak exotherm temperature T3 of from 220 to 275° C. when a 10 mL sample of the third curable mixture is cured in air at a curing temperature of 70° C.

20. A curable epoxy resin adhesive according to claim 19 wherein the third curing property further comprises (c3) a third time period P3 from initiation of curing to peak exotherm temperature, wherein the third time period P3 is from 550 to 850 seconds measured when the curing is carried out in air at a curing temperature of 70° C. and on a resin sample having a volume of 10 mL.

21. A curable epoxy resin adhesive according to claim 20 wherein the third time period P3 is from 675 to 825 seconds.

22. A curable epoxy resin adhesive according to claim 19 wherein the third curing property comprises (c3) a glass transition temperature Tg2 of the cured epoxy resin which is within the range of from 88 to 98° C. after a curing time period of 5 hours at a curing temperature of 70° C. in air.

23. A curable epoxy resin adhesive according to claim 1 wherein the weight ratio of the first amine curing agent to the second amine curing agent is within the range of from 1:2 to 1:4.

24. A curable epoxy resin adhesive according to claim 23 wherein the weight ratio of the first amine curing agent to the second amine curing agent is within the range of from 1:2.5 to 1:3.5.

25. A curable epoxy resin adhesive according to claim 1 wherein the curing agent component comprises from 3 to 7 wt % of the first amine curing agent and from 9 to 21 wt % of the second amine curing agent, each based on the total weight of the curing agent component.

26. A curable epoxy resin adhesive according to claim 25 wherein the curing agent component comprises from 4 to 5.5 wt % of the first amine curing agent and from 12 to 16.5 wt % of the second amine curing agent, each based on the total weight of the curing agent component.

27. A curable epoxy resin adhesive according to claim 1 wherein the curable epoxy resin adhesive, which comprises both the epoxy resin component and the curing agent component, comprises from 0.9 to 1.5 wt % of the first amine curing agent and from 2.7 to 4.5 wt % of the second amine curing agent, each based on the total weight of the curable epoxy resin adhesive.

28. A curable epoxy resin adhesive according to claim 1 wherein the test epoxy resin is a diglycidyl ether bisphenol-A (DGEBA) epoxy resin.

29. A curable epoxy resin adhesive according to claim 28 wherein the test epoxy resin is liquid at 25° C. and has an epoxy equivalent weight (EEW) within the range of from 175 to 200, and is optionally about 187.

30.-42. (canceled)

43. A curable epoxy resin adhesive according to claim 1 wherein the epoxy resin component has an overall epoxy equivalent weight (EEW) of from 175 to 300 g/eq.

44. A curable epoxy resin adhesive according to claim 1 wherein the epoxy resin component has an overall epoxy equivalent weight (EEW) of from 175 to 300 g/eq, the first amine curing agent comprises a modified or adducted triethylene tetramine having a first amine functionality corresponding to an active hydrogen equivalent weight (AHEW) of from 42-54, the second amine curing agent comprises a linear, asymmetrically branched or cyclic aliphatic diamine or triamine having a second amine functionality which corresponds to an active hydrogen equivalent weight (AHEW) of from 15-40, and the weight ratio of the first amine curing agent to the second amine curing agent is within the range of from 1:2 to 1:4.

Description

[0029] Preferred embodiments of the present invention will now be described by way of example only with reference to the accompanying drawings, in which:—

[0030] FIGS. 1a and 1b are graphs which schematically show the relationship between temperature and time during both working and subsequent curing for, respectively, a known curable epoxy resin adhesive and a curable epoxy resin adhesive in accordance with an embodiment of the present invention;

[0031] FIG. 2 is a perspective view of a syringe used to test the curing properties of a modelled curable epoxy adhesive in accordance with the present invention; and

[0032] FIG. 3 is a graph which shows the relationship between temperature and time during curing for each of three examples of a curable epoxy adhesive in accordance with embodiments of the present invention, and for curable epoxy adhesives not in accordance with the present invention.

[0033] In accordance with the present invention there is provided a curable epoxy resin adhesive.

[0034] The present invention has particular application for use as an adhesive for bonding together large structural parts, for example structural elements of wind turbine blades during manufacture of the wind turbine blade, or parts of marine vessels or civil engineering structures, for which a long working time at ambient temperature for the uncured mixture of the resin and hardener components is desired, in combination with a fast curing time at an elevated curing temperature.

[0035] Epoxy resins exhibit excellent adhesive properties and mechanical properties. Therefore the epoxy resins used in the preferred embodiments of the present invention can easily meet the adhesive bonding requirements to enable an epoxy resin adhesive layer to bond strongly to materials used in wind blade manufacture, such as a fibre-reinforced resin matrix composite material, for example an epoxy resin matrix composite reinforced with glass or carbon fibres, or a core material, for example the surface of a polymeric cellular foam (e.g. PET structural foam), balsa or honeycomb (e.g. Nomex® honeycomb) core material.

[0036] FIG. 1b, like FIG. 1a, is a graph which schematically shows the relationship between temperature and time during both working and subsequent curing for a curable epoxy resin adhesive in accordance with an illustrative example of the present invention. The working time at low ambient temperature, such as 20° C. as shown, is in this example about 150 minutes. At the end of the working time the temperature rapidly increases as a result of applying an external heat source to initiate exothermic curing of the epoxy resin, for example by heating to an applied temperature of 70° C. Thereafter the resin cures during a cure period. In this example the cure period is about 175 minutes.

[0037] As compared to the known resin of FIG. 1a, the modified epoxy resin system comprising a curing agent mixture has increased the working time and decreased the cure time, without compromising the mechanical properties of the cured resin. The longer working time has particular utility when bonding large surface areas. The shorter cure time reduces the overall curing cycle time, which can achieve cost savings both for operational production costs and for capital investment costs.

[0038] The curable epoxy resin adhesive comprises an epoxy resin component and a curing agent component. The epoxy resin component and the curing agent component are made and sold in a separated form. During use of the adhesive, a mixture of the epoxy resin component and the curing agent component is formed, as is well known in the art of thermosetting resins, with the epoxy resin component and the curing agent component being mixed at a predetermined ratio, typically a weight ratio, so that the curing agent provides the required number of reactive groups to react with the number of epoxide groups present in the amount of epoxy resin to be cured. The mixture is then usually heated to an elevated curing temperature, which causes curing of the epoxy resin component by the curing agent component, to form the cured adhesive. A typical curing temperature for a curable epoxy resin adhesive is within the range of from 50 to 100° C., for example 70° C.

[0039] The epoxy resin component comprises at least one epoxide-containing resin. The at least one epoxide-containing resin is typically selected from at least one of a bisphenol-based epoxy resin, an epoxy novolac resin, an epoxy cresol novolac resin and an epoxy phenol novolac resin, or a mixture of any two or more thereof. Epoxy resins of different epoxide functionality, and/or different epoxide equivalent weight (EEW) may be blended to achieve desired properties in both the curable resin and the cured resin, as is well known in the art. Typically, the epoxy resin component as an overall epoxy equivalent weight (EEW) of from 175 to 300 g/eq.

[0040] The curing agent component comprises a mixture of a first amine curing agent and a second amine curing agent. In this specification, the properties of the first and second amine curing agents are relevant to the present invention, although the curing agent component may comprise at least one additional amine curing agent. Typically, the curing agent component is present in the curable epoxy adhesive in a concentration of from 20 to 50 parts by weight curing agent component to 100 parts by weight epoxy resin component to provide the total weight of the curable epoxy adhesive. The curing agent component and/or the epoxy resin component may comprise additional ingredients, such as fillers, diluents, etc, Too low an amount of the curing agent component may cause a reduced cure of the epoxy resin material, whereas too high an amount may cause an excessively exothermic cure, reduced Tg and reduced mechanical properties.

[0041] The present invention is based upon the finding by the present inventors that by providing a specific mixture of specific first and second amine curing agents, a first amine curing agent which provides a “long” working time can be used which on its own would also provide a “long” cure time, and the cure time can be significantly shortened, without compromising or significantly reducing the “long” working time, by mixing, together with the first amine curing agent, a second amine curing agent which on its own (a) is more latent at ambient temperature than the first amine curing agent and (b) is more exothermic during curing than the first amine curing agent.

[0042] The higher exothermic curing of the second amine curing agent raises the temperature of the curing resin as compared to the use of the first amine curing agent alone, and the increased temperature accelerates the curing of the resin by the curing agent mixture. However, since the second amine curing agent is more latent at ambient temperature than the first amine curing agent, the working time of the resin comprising the curing agent mixture is not reduced by addition of the second amine curing agent.

[0043] In other words, by providing a mixture of the first and second amine curing agents having a specific relationship between their individual properties, in particular the functional curing property of each of the respective first and second amine curing agents with respect to the epoxy resin component, the overall functional curing property of the epoxy resin component in the adhesive can be modified.

[0044] Such modification can provide improved epoxy resin adhesives because by providing a mixture of the specific first and second amine curing agents, the resultant amine-cured epoxy systems does not adopt a curing profile close to a first order kinetics model, whereby both the working time and the cure time tend to increase or decrease together in a linear relationship with any change in temperature.

[0045] In contrast, the epoxy resin adhesives formulated according to the present invention can independently decrease the cure time without decreasing the working time, for any given curing temperature, as compared to an adhesive comprising only one curing agent, or a blend of curing agents that provides a curing profile close to a first order kinetics model.

[0046] In practical terms, for example, an adhesive that is suitable for manufacturing wind turbine blades and comprises a known amine curing agent system, for example the Applicant's known adhesive as described above, can be modified, by use of the curing agent mixture of the first and second curing agents, to maintain or even increase the working time and additionally reduce the cure time, for example reduce the cure time from 5 hours to 2 hours using a curing temperature of 70° C.

[0047] In accordance with the present invention, the functional curing property of each of the respective first and second amine curing agents with respect to the epoxy resin component, is important to achieve the resultant overall functional curing property of the epoxy resin component by the mixture of the first and second amine curing agents.

[0048] As is well known to those skilled in the art, the reactivity of an amine curing agent used for curing epoxy resins, and the final properties of the cured polymer, can be made to vary significantly depending on the number, type, and position of the reactive —NH.sub.x groups within the amine curing agent In particular, the degree of electronic effects, such as electron delocalisation, and steric hindrance can affect the reactivity of an amine curing agent.

[0049] In accordance with preferred embodiments of the present invention, the first amine curing agent may be considered to be a “base” amine curing agent which, when used alone, can provide any desired working time and final properties of the cured polymer resin. Additional curing agents may be used in addition to the first curing agent to provide a “base” amine curing agent blend which, when used, can provide the desired working time and final properties of the cured polymer resin.

[0050] In contrast, the second amine curing agent may be considered to be a “modifier” amine curing agent which, when mixed with the first amine curing agent to substitute for a portion of the first amine curing agent, provides a combined amine curing agent system which does not shorten the working time, but does shorten the cure time, of the epoxy resin adhesive comprising only the “base” amine curing agent. Alternatively, the cure time may be unchanged and the working time is lengthened.

[0051] Consequently, the “base” amine curing agent is not limited to any particular chemical structure for the first amine curing agent. The first amine curing agent may have any desired chemical structure, for example already known to those skilled in the art for use as an amine curing agent for epoxy resins, to achieve the desired cured resin properties with associated working and cure times. In some preferred embodiments, the first amine curing agent comprises a modified or adducted triethylene tetramine. However, other “base” amine curing agents may be used as the first amine curing agent.

[0052] A preferred first amine curing agent is available in commerce from Bitrez under the trade name Curamine® 31-706; this amine curing agent is a modified TETA (triethylene tetramine), in particular an amine adduct of triethylene tetramine. As described above, additional curing agents may be used in addition to the first curing agent to provide a “base” amine curing agent blend which, when used, can provide the desired working time and final properties of the cured polymer resin. The “base” amine curing agent blend may comprise the modified TETA in combination with a cycloaliphatic amine based curing agent, for example isophorone diamine.

[0053] However, the second amine curing agent is required to be latent at ambient temperature but have a high peak exothermic temperature during curing. Consequently, the second amine curing agent is a diamine which has the formula NH.sub.2—R—NH.sub.2 where R is any aliphatic or cycloaliphatic constituent, which is either unsubstituted or substituted with at least one functional group, or where R is any aromatic constituent, which is either unsubstituted or substituted with at least one functional group.

[0054] In some preferred embodiments of the present invention, the second amine curing agent comprises a linear, asymmetrically branched or cyclic aliphatic diamine or triamine. For example, in some preferred embodiments of the present invention the second amine curing agent comprises 2-methylpentane-1,5-diamine, octane-1,8-diamine, cyclohexane-1,2-diamine, N.sup.1-(3-aminoethyl)ethane-1,2-diamine, N.sup.1-(3-aminopropyl)propane-1,3-diamine, 2,2,-(diaminoethyl) propane-1,2-diamine, 2,2,-dimethyl propane-1,3-diamine, octamethylenediamine, ethylenediamine, 1,3-diaminopropane, 1,2-prollenediamine, diethylenetriamine, dipropylene triamine, N,N-Bis-(3-amineopropyl)methylamine, 1,2-cyclohexane diamine, or any mixture of one or more thereof. However, other diamines may be used to provide the functional properties of the second amine curing agent according to the present invention.

[0055] A preferred second amine curing agent is available in commerce from Invista under the trade name Dytek® A; this amine curing agent is 2-methylpentane-1,5-diamine. An alternative preferred second amine curing agent is available in commerce from Invista under the trade name Dytek® DCH-99; this amine curing agent is 1,2-cyclohexane diamine.

[0056] In other preferred embodiments of the present invention, the second amine curing agent comprises a di(aminoalkyl) benzene, wherein each alkyl group has from 1 to 3 carbon atoms and the alkyl groups are the same or different in each aminoalkyl functional group. For example, in some preferred embodiments of the present invention the second amine curing agent comprises xylylenediamine, such as 1,3-Bis(aminomethyl)benzene (m-xylylenediamine) or 1,4-Bis(aminomethyl)benzene (p-xylylenediamine), a di(aminoethyl) benzene such as 1,3-Bis(aminoethyl)benzene or 1,4-Bis(aminoethyl)benzene, or a di(aminopropyl) benzene such as 1,3-Bis(aminopropyl)benzene or 1,4-Bis(aminopropyl)benzene.

[0057] The second amine curing agent preferably comprises xylylenediamine, such as 1,3-Bis(aminomethyl)benzene (m-xylylenediamine) or 1,4-Bis(aminomethyl)benzene (p-xylylenediamine), A particularly preferred second amine curing agent is 1,3-Bis(aminomethyl)benzene (m-xylylenediamine) which is widely available in commerce under CAS Number 1477-55-0. This amine curing agent is also called m-XDA, or sometimes MXDA.

[0058] In some preferred embodiments of the present invention, the first amine curing agent, or the blend of the first amine curing agent and any additional amine curing agent to form a “base” amine curing agent blend, has a first amine functionality corresponding to an active hydrogen equivalent weight (AHEW) of from 42-54 and the second amine curing agent has a second amine functionality which is higher than for the first amine curing agent and corresponds to an active hydrogen equivalent weight (AHEW) of from 15-40. As is known to those skilled in the art, AHEW=amines (Active Hydrogen Equivalent Weight)=molecular weight/number of amine reactive sites e.g. NH=1, NH2=2, NR=0.

[0059] Typically, the curing agent component comprises from 15 to 60 wt % of the first amine curing agent and from 40 to 85 wt % of the second amine curing agent, each based on the total weight of the first and second amine curing agents. In some preferred embodiments, the curing agent component comprises from 20 to 50 wt % of the first amine curing agent and from 50 to 80 wt % of the second amine curing agent, each based on the total weight of the first and second amine curing agents. As explained above, the curing agent components typically comprises additional ingredients in addition to the first and second amine curing agents.

[0060] Typically, the weight ratio of the first amine curing agent to the second amine curing agent is within the range of from 1:2 to 1:4, for example from 1:2.5 to 1:3.5, preferably about 1:3.

[0061] Typically, the curing agent component comprises from 3 to 7 wt % of the first amine curing agent and from 9 to 21 wt % of the second amine curing agent, each based on the total weight of the curing agent component. In some preferred embodiments, the curing agent component comprises from 4 to 5.5 wt % of the first amine curing agent and from 12 to 16.5 wt % of the second amine curing agent, each based on the total weight of the curing agent component.

[0062] Typically, the curable epoxy resin adhesive, which comprises both the epoxy resin component and the curing agent component, comprises from 0.9 to 1.5 wt % of the first amine curing agent and from 2.7 to 4.5 wt % of the second amine curing agent, each based on the total weight of the curable epoxy resin adhesive.

[0063] In accordance with the present invention, the first amine curing agent has a first curing property determined by mixing the first amine curing agent alone with a test epoxy resin component to form a first curable mixture.

[0064] The test epoxy resin is one epoxide-containing resin of the epoxy resin component that is present in a concentration of more than 50 wt % of the at least one epoxide-containing resin. Preferably, the test epoxy resin is a diglycidyl ether bisphenol-A (DGEBA) epoxy resin. Preferably, the test epoxy resin is liquid at 25° C. Preferably, the test epoxy resin has an epoxy equivalent weight (EEW) within the range of from 175 to 200, and is optionally about 187.

[0065] The first curing property comprises (a1) a first gel time G1 when a 150 g sample of the first curable mixture is at an ambient temperature of 25° C. and (b1) a first peak exotherm temperature T1 when a 10 mL sample of the first curable mixture is cured in air at a curing temperature of 70° C. In contrast, the second curing agent has a second curing property determined by mixing the second amine curing agent alone with the test epoxy resin to form a second curable mixture. The second curing property comprises (a2) a second gel time G2 when a 150 g sample of the second curable mixture is at an ambient temperature of 25° C. and (b2) a second peak exotherm temperature T2 when a 10 mL sample of the second curable mixture is cured in air at a curing temperature of 70° C.

[0066] In accordance with the present invention, a ratio G2:G1 between the first and second gel times is from 4-15:1 and the second peak exotherm temperature T2 is higher than the first peak exotherm temperature T1 by a temperature Δt, wherein Δt is at least 2° C., optionally at least 5° C.

[0067] Typically, Δt is from 2 to 30° C., optionally from 2 to 25° C. In some preferred embodiments of the present invention, the first peak exotherm temperature T1 is within the range of from 220 to 240° C. and/or the second peak exotherm temperature T2 is within the range of from 235 to 270° C. For example, the first peak exotherm temperature T1 is within the range of from 230 to 240° C. and/or the second peak exotherm temperature T2 is within the range of from 237 to 265° C.

[0068] The ratio G2:G1 between the first and second gel times means that the second curing agent is significantly more latent at ambient temperature than the first amine curing agent. This in turns provides that the second curing agent does not decrease, and may increase, the working time at ambient temperature, i.e. 25° C., and the working time at even higher working temperatures, such as 40° C., that are typically encountered during commercial use, as compared to when only the first amine curing agent is used.

[0069] It has unexpectedly been found by the present inventors that the addition of the more latent second curing agent resulted in a higher peak exotherm temperature. This result is unexpected because amine-epoxy systems known in the art tend to exhibit lower peak exotherm temperatures for more latent amine curing agent systems.

[0070] The peak exotherm temperature, and the increase in peak exotherm temperature, are measurable parameters of curable resins that are directly related to the reactivity of the amine curing agent system with the epoxy resin component that is being cured.

[0071] The positive temperature difference Δt between the respective peak exotherm temperatures of the second and first amine curing agents means that the second curing agent is more exothermic, optionally significantly more exothermic, during curing at the curing temperature than the first amine curing agent. This in turns provides that the second curing agent decreases the cure time at the elevated (compared to ambient temperature) curing temperature as compared to when only the first amine curing agent is used.

[0072] In some preferred embodiments of the present invention, the ratio G2:G1 between the first and second gel times is from 6:1-10:1. Typically, the first gel time G1 is from 15 to 35 minutes and the second gel time G2 is from 100 to 300 minutes; for example the first gel time G1 is from 20 to 30 minutes and the second gel time G2 is from 150 to 250 minutes.

[0073] Preferably, the first curing property further comprises (c1) a first time period P1 from initiation of curing to peak exotherm temperature and the second curing property further comprises (c2) a second time period P2 from initiation of curing to peak exotherm temperature, wherein P2 is greater than P1 by a time period ΔP of at least 100 seconds measured when the curing is carried out in air at a curing temperature of 70° C. and on a resin sample having a volume of 10 mL. Typically, the time period ΔP is from 150 to 425 seconds, optionally from 150 to 410 seconds, further optionally from 250 to 410 seconds.

[0074] This functional property means that the second curing agent can take longer to attain a higher peak exotherm temperature than the time taken by the first curing agent to attain a lower peak exotherm temperature. This in turn provides that the curing by the second curing agent can progressively generate exothermic heat which accelerates the curing action of the first curing agent, and the combined technical effect is that the cure time of the curable epoxy adhesive is reduced.

[0075] In some preferred embodiments of the present invention, the curing agent component, i.e. the mixture of the first and second amine curing agents, has a third curing property determined by mixing the curing agent component with the epoxy resin component to form a third curable mixture. The third curing property comprises (a3) a gel time G3 of from greater than 28 minutes to up to 90 minutes when a 150 g sample of the third curable mixture is at an ambient temperature of 25° C., wherein the gel time G3 is between gel times G1 and G2, and (b3) a peak exotherm temperature T3 of from 220 to 275° C. when a 10 mL sample of the third curable mixture is at a curing temperature of 70° C.

[0076] It has unexpectedly been found by the present inventors that the addition of the more latent second amine curing agent to the first amine curing agent can result in a working time for the combined amine curing agent which is between the individual working times of the first and second amine curing agents, yet the peak exotherm temperature using the combined amine curing agent can be higher than the individual peak exotherm temperatures of the first and second amine curing agents, and with a faster cure time using the combined amine curing agent as compared to the first amine curing agent.

[0077] In some preferred embodiments of the present invention, the third curing property further comprises a time period (P3) from initiation of curing to peak exotherm temperature for the combined amine curing agent is from 550 to 850 seconds, for example from 675 to 825 seconds, measured when the curing is carried out in air at a curing temperature of 70° C. and on a resin sample having a volume of 10 mL.

[0078] In some preferred embodiments of the present invention, the first curing property further comprises (c1) a glass transition temperature Tg2 of the cured epoxy resin which is within the range of from 94 to 98° C. after a curing time period of 5 hours at a curing temperature of 70° C. in air and the second curing property further comprises (c2) a glass transition temperature Tg2 of the cured epoxy resin which is within the range of from 87 to 93° C. after a curing time period of 5 hours at a curing temperature of 70° C. in air.

[0079] In some preferred embodiments of the present invention, the third curing property further comprises (c3) a glass transition temperature Tg2 of the cured epoxy resin which is within the range of from 88 to 98° C. after a curing time period of 5 hours at a curing temperature of 70° C. in air. This provides that the cured adhesive can have a high Tg2, and therefore has high mechanical properties associated with a high degree of curing and crosslinking.

[0080] It has unexpectedly been found by the present inventors that the addition of the second amine curing agent can provide a high Tg2 to the cured epoxy resin even though the working time can be relatively long. The addition of the second amine curing agent to the first amine curing agent can provide a shorter cure time without any decease in working time and without any significant decrease in the Tg2 of the cured epoxy resin. In other words, the addition of the second amine curing agent can shorten cure time without any detriment to the mechanical properties of the cured resin.

[0081] When the second amine curing agent is an aliphatic or cycloaliphatic diamine, the combination of the first and second amine curing agents can provide a short cure time and a long working time when the working time is measured at a typical ambient working temperature of 25° C. When the second amine curing agent is an aromatic diamine, the combination of the first and second amine curing agents can provide a short cure time and a long working time when the working time is measured at a higher-than-ambient working temperature of typically 40° C. In other words, the selection of an aromatic diamine as the second amine curing agent permits a higher working temperature to be used without any significant reduction in the working time or increase in the cured time, as compared to the selection of an aliphatic or cycloaliphatic diamine as the second amine curing agent. Also, the selection of an aromatic diamine as the second amine curing agent permits a higher peak exotherm temperature, and a higher Tg2 associated with good mechanical properties, to be achieved as compared to the selection of an aliphatic or cycloaliphatic diamine as the second amine curing agent.

[0082] In some embodiments of the present invention, the epoxy resin adhesive may further comprise an accelerator, which may be formulated so that the epoxy resin may be cured at a selected curing temperature and/or to modify the Tg2 of the cured resin. Any known accelerator may optionally be added to the adhesive, as known to those skilled in the art.

[0083] The curable epoxy resin adhesive may further comprise any other known additives, such as a rheology modifier, as known to those skilled in the art. The rheology modifier may typically comprises at least one of a thermoplastic resin and an inorganic particulate thickener or a mixture thereof. Inorganic fillers such as calcium carbonate, fumed silica, wetting additives, air release additives, coupling agents, etc may additionally or alternatively be present in any combination as is well known to those skilled in the art of epoxy resin adhesives.

[0084] The present invention further provides a method of manufacturing a curable epoxy resin adhesive. The method comprises the steps of: [0085] i. providing the epoxy resin component, which comprises at least one epoxide-containing resin, as described above; [0086] ii. providing a first amine curing agent, as described above; [0087] iii. providing a second amine curing agent, as described above, wherein a ratio G2:G1 between the first and second gel times is from 4-15:1 and the second peak exotherm temperature T2 is higher than the first peak exotherm temperature T1 by a temperature Δt, wherein Δt is at least 2° C.; [0088] iv. mixing together the first and second amine curing agents to produce a curing agent component, wherein the curing agent component comprises from 15 to 60 wt % of the first amine curing agent and from 40 to 85 wt % of the second amine curing agent, each based on the total weight of the first and second amine curing agents; and [0089] v. providing both the epoxy resin component and the curing agent component in a separated form thereby to provide the curable epoxy resin adhesive, wherein providing a mixture of the epoxy resin component and the curing agent component at a curing temperature of the adhesive causes curing of the epoxy resin component by the curing agent component.

[0090] As described above, optionally the curing agent component produced in step iv has a third curing property determined by mixing the curing agent component with the epoxy resin component to form a third curable mixture, the third curing property comprising (a3) a gel time G3 of from greater than 28 minutes to up to 90 minutes when a 150 g sample of the third curable mixture is at an ambient temperature of 25° C., wherein the gel time G3 is between gel times G1 and G2, and (b3) a peak exotherm temperature T3 of from 220 to 275° C. when a 10 mL sample of the third curable mixture is cured in air at a curing temperature of 70° C.

[0091] The present invention further provides a use of the curable epoxy resin adhesive according to the present invention, or produced by the method according to the present invention, for bonding together structural parts of a wind turbine blade, a marine vessel or a civil engineering structure.

[0092] The preferred embodiments of the present invention will now be described further with reference to the following non-limiting Examples.

EXAMPLES 1 TO 3

[0093] A first amine curing agent, called Curing agent #1, was provided. The first curing agent is available in commerce from Bitrez under the trade name Curamine® 31-706; this amine curing agent is a modified TETA (triethylene tetramine), in particular an amine adduct of triethylene tetramine.

[0094] A second amine curing agent, called Curing agent #2, was also provided. The second amine curing agent is available in commerce from Invista under the trade name Dytek® A; this amine curing agent is 2-methylpentane-1,5-diamine. The second curing agent had an AHEW of 29 g/eq.

[0095] Three different mixtures, called Blends A, B and C, of the first and second amine curing agents were formulated as Examples 1 to 3 respectively, and the weight ratios in the mixtures are shown in Table 1 below.

TABLE-US-00001 TABLE 1 Example 1 Example 2 Example 3 Blend A Blend B Blend C Curing agent #2 - DYTEK A 25 wt % 50 wt % 75 wt % Curing agent #1 - Curamine 31-706 75 wt % 50 wt % 25 wt %

[0096] The properties of the individual Curing agents #1 and #2, and of the Blends A, B and C of the individual Curing agents #1 and #2, were then measured and the results are shown in Table 2. In particular, a single epoxy resin, to be used for an epoxy resin adhesive composition, was provided.

[0097] In order to simulate actual applications during use of the adhesive, and to determine the absolute and relative working and curing properties of the first and second amine curing agents, the first and second curing agents were tested in a modelled epoxy resin system. The modelled epoxy resin system comprised a test hardener, including the curing agent(s) to be tested, and a test epoxy resin, including at least one epoxy resin that is to be used in the final epoxy resin adhesive composition. The use of such a modelled epoxy resin system comprising a test hardener and a test epoxy resin enables reliable and repeatable test results to be readily achieved in order to be able to determine the absolute and relative curing properties of the first and second amine curing agents. The modelled epoxy resin system is a simplified version of the adhesive formulation, without addition of fillers or other additives, and the working and curing behaviour of the modelled epoxy resin system represents the working and curing behaviour of the final adhesive formulation.

[0098] In the modelled epoxy resin system the test hardener consisted of the amine(s) to be tested and the test epoxy resin consisted of a single epoxy resin, typically a diglycidyl ether bisphenol-A (DGEBA) epoxy resin which is liquid at 25° C., that is to be comprised in the final curable epoxy resin adhesive as a primary epoxy resin ingredient, i.e. the test epoxy resin comprises greater than 50 wt % of the at least one epoxy resin(s) in the epoxy resin component of the of the final adhesive formulation.

[0099] For all of the measurements within Table 2 below which used the modelled epoxy resin system, the epoxy resin component used was a diglycidyl ether bisphenol-A (DGEBA) liquid epoxy resin with an Epoxy Equivalent Weight (EEW) of 187 (g/eq). The epoxy resin was mixed with either the single amines or amine blends as described above to provide a total weight of curable resin of 150 g.

[0100] Each of the individual Curing agents #1 and #2, and Blends A, B and C of the individual Curing agents #1 and #2, were respectively mixed with the test epoxy resin at a weight ratio to provide a full curing reaction between the amine reactive groups in the curing agent and the epoxide groups in the test epoxy resin. The respective proportions to provide a total weight of 150 g for each tested curable epoxy resin are shown in Table 2.

[0101] Immediately after the mixing, each of the amine curing agent adhesive mixtures was tested to measure the viscosity at 25° C. using a Brookfield CaP 2000 LT viscometer according to the settings in Table 2. The measured viscosity values, as well as the rotational speed of the spindle of the viscometer, are shown in Table 2.

TABLE-US-00002 TABLE 2 Agent #2 Agent #1 DYTEK A 31-706 Blend A Blend B Blend C Measured Viscosity (cP) 15 810 195 22.5 7 CaP Settings Cone 1, Cone 1, Cone 1, Cone 1, Cone 1, 2000 rpm 150 rpm 900 rpm 2000 rpm 900 rpm @ 25° C. @ 25° C. @ 25° C. @ 25° C. @ 25° C. Tg 2 by DSC 5 hrs @ 90.7 96.2 90 96.2 89.6 70° C. (° C.) DGEBA Liquid Epoxy (g) 129.9 118.4 122.3 125.4 127.9 Amine curing agent (g) 20.1 31.6 27.7 24.6 22.1 150 g TECAM Geltime @ 200 26 28.7 47 57.4 25° C. in a water bath (mins)

[0102] In addition, each of the curable epoxy resin/amine curing agent adhesive mixtures was tested to measure, by differential scanning calorimetry (DSC), the Tg2 of the resultant cured epoxy resin adhesive after a period of 5 hours curing at an applied elevated curing temperature of 70° C. The measured Tg2 values are shown in Table 2.

[0103] Furthermore, the TECAM geltime at a temperature of 25° C. for each curable epoxy resin/amine curing agent adhesive mixture was measured. The geltime is representative of the working time of the resin at ambient temperature.

[0104] The testing protocol was as follows: 150 g of the epoxy resin/amine curing agent adhesive mixture in an open-topped container was placed within a 25° C. (+/−0.2° C.) waterbath. A commercially available Gelation Timer, available in commerce from Techne under the trade name Techne® FGT6, was then used to determine the point at which the mixed system reaches gelation point. A buoyant plunger is suspended in the heated resin from a driven mechanism imparting simple harmonic motion of fixed amplitude in a vertical plane and coupled so that the plunger is positively raised during the upstroke, but is free to fall at a rate not faster than the simple harmonic motion on the down stroke. The gelation time is measured as the period between completion of the addition of all appropriate curing agents to the resin system and the automatic detection of the movement when gelation of the resin becomes sufficient for the mixture just to support the plunger. The standard protocol of the Techne® FGT6 Gelation Timer was used which provides an accuracy of the gelation time, i.e. the “geltime”, to within +/2%.

[0105] Table 2 shows that Curing agent #1 exhibited a short geltime of 26 minutes, whereas Curing agent #2 exhibited a long geltime of 200 minutes. The geltimes of Blends A, B and C are between the geltimes of Curing Agents #1 and #2, with the geltimes of Blends B and C being significantly greater than the geltime of Curing Agent #1. In other words, adding Curing agent #2 to substitute for a portion of Curing Agent #1 increased the working time of the curable epoxy adhesive.

[0106] It may be seen unexpectedly that the Tg2 of the resin using Blend B, a 50:50 wt % mixture of Curing Agents #1 and #2, is substantially the same as the Tg2 of the resin using the Curing Agent #1. In other words, for this Blend B the mechanical properties of the cured epoxy resin are not reduced despite the increase in working time. This shows that adding a second amine curing agent, which is an aliphatic diamine in accordance with this embodiment of the present invention, which is more latent than the base first amine curing agent can increase the working time without compromising the mechanical properties of the cured resin.

[0107] In further testing, the enthalpy of reaction was investigated for each of the resin formulations of Table 2.

[0108] When an epoxy resin adhesive composition is cured over a large surface area, for example during manufacture of a wind turbine blade, the large bond area provides a thermal system during curing which is pseudo-adiabatic (i.e. the resin being cured does not gain or lose significant thermal energy to the bonded parts or environment during curing) due to the relatively large bond areas.

[0109] In the present specification, the curing time of the modelled epoxy resin system was tested using specific curing parameters on a specific volume of the test epoxy resin, as described hereinabove, in order to achieve a reliable and repeatable test protocol. This specific test was employed to measure the following parameters in the modelled epoxy resin system for the first and second amine curing agents, individually and in combination: peak exotherm temperature during curing, time period from initiation of curing to peak exotherm temperature during curing, and glass transition temperature Tg2 of the cured resin.

[0110] The modelled epoxy resin system again used a test hardener which consisted of the amine(s) to be tested and a test epoxy resin which consisted of a single epoxy resin, typically a diglycidyl ether bisphenol-A (DGEBA) epoxy resin, that is to be comprised in the final curable epoxy resin adhesive as a primary epoxy resin ingredient, i.e. the test epoxy resin comprises greater than 50 wt % of the at least one epoxy resin(s) in the epoxy resin component of the of the final adhesive formulation. Preferably, the diglycidyl ether bisphenol-A (DGEBA) epoxy resin that is the test epoxy resin is liquid at 25° C. Preferably, the diglycidyl ether bisphenol-A (DGEBA) test epoxy resin has an epoxy equivalent weight (EEW) within the range of from 175 to 200, for example about 187.

[0111] The modelled epoxy resin system used the following method for recording the peak exotherm temperature during curing and the time period from initiation of curing to peak exotherm temperature during curing:

1. The test epoxy resin and test hardener comprising the amine(s) to be tested are mixed/blended using a mixing machine having preset mixing time and mixing speed which are used for all tests and ensure complete mixing of the ingredients.
2. 10 mL of the mixed blend are then drawn into a conventional polymeric syringe (10) having an inner diameter of 14.5 mm and a volume scale marked along the length of the syringe, as shown in FIG. 2.
3. As shown in FIG. 2, a thermocouple wire (12) is introduced into the outlet aperture of the syringe to record temperature at the 5 mL marking on the volume scale in order to record the temperature at the centre of the volume of the liquid.
4. The syringe is introduced into an oven set at 70° C., and the air temperature of the oven is monitored during the length of the test protocol using conventional temperature measurement software (for example from Pico™).
5. The temperature measurement software is used to record the time and temperature of the exothermic curing reaction within the syringe.

[0112] This test protocol was used to test 10 mL samples, provided in a respective syringe, of each tested curable epoxy resin adhesive of Blends A, B and C which were reactively cured in air and within an oven at an applied elevated curing temperature of 70° C., and the resulting increase in temperature and associated time, were recorded.

[0113] In this specification, each value of exotherm temperature, and time taken to reach the peak exotherm temperature, was measured using this protocol, i.e. by curing in air at 70° C. a 10 mL sample, typically in a syringe of the curable epoxy resin adhesive composition.

[0114] The results are shown in FIG. 3 which shows the relationship between temperature and time during curing for each of Blends A, B and C. The peak exotherm temperature and the time period to reach the peak exotherm temperature are also listed in Table 3. Table 3 also lists the geltimes measured at 25° C. as specified above.

TABLE-US-00003 TABLE 3 Peak Exotherm Time To Peak Geltime @ Temperature Temperature 25° C. (° C.) (seconds) (minutes) Curing Agent #1 236.46 539 26 CURAMINE 31-706 Curing Agent #2 259.50 794 200 DYTEK A Blend A 196.93 633 28.7 Blend B 222.45 696 47 Blend C 237.79 783 57.4 Comparative 175.03 1814 598 Example 1 JEFFAMINE D230

[0115] FIG. 3 and Table 3 show, again unexpectedly, that the more latent systems, resulting from higher concentrations of the Dytek A amine curing agent, i.e. Curing agent #2, experienced higher peak exotherm temperatures. This is contrary to what would be expected from known amine epoxy systems from which it is generally known that slower or more latent systems typically have lower peak exotherm temperatures.

[0116] The present inventors therefore have found unexpectedly that by using a more latent amine blend, a higher exotherm temperature can be realised during adhesive cure. Since the adhesive reactivity is proportional to temperature, the higher temperature to which the curable resin is exposed during cure will result in a faster cure rate and/or higher Tg of the resultant cured epoxy resin.

[0117] It can also be seen from FIG. 3 and Table 3 that the time period P3 from curing initiation to peak exotherm temperature for each of Blends A, B and C is within the range of from 550 to 850 seconds measured when the curing is carried out in air at a curing temperature of 70° C. and on a resin sample having a volume of 10 mL which is cured in a syringe.

[0118] Blend C, having the highest proportion of Curing agent #2, exhibited the highest peak exotherm temperature and the longest time period P3 from curing initiation to peak exotherm temperature of each of Blends A, B and C.

[0119] FIG. 3 and Table 3 show that Blends B and C having the highest proportions, 50 wt % and 75 wt % respectively, of Curing agent #2 exhibited the higher peak exotherm temperatures of Blends A to C. The higher peak exotherm temperature of Blend C is higher than the peak exotherm temperature attained by the base Curing Agent #1, and is attained after the peak exotherm temperature attained by the base Curing Agent #1.

[0120] This shows that addition of the Curing agent #2 to the base Curing Agent #1 can achieve equivalent cure time, with the same or enhanced mechanical properties, yet with increased working time.

EXAMPLE 4

[0121] The same first amine curing agent as used in Examples 1-3, called Curing agent #1, was provided.

[0122] A different second amine curing agent was used as compared to Examples 1-3, which was called Curing agent #2a. The second amine Curing agent #2a was m-xylylenediamine, and is available in commerce under CAS number 1477-55-0. The second curing agent #2a had an AHEW of 34 g/eq.

[0123] One mixture, called Blend D, of the first and different second amine curing agents were formulated as Example 4, and the weight ratios in the mixture are shown in Table 4 below.

TABLE-US-00004 TABLE 4 Example 4 Blend D Curing agent #2a - m-xylylenediamine 75 wt % Curing agent #1 - Curamine 31-706 25 wt %

[0124] The properties of the individual Curing agents #1 and #2a, and of the Blend D, were measured using the test procedures as described above for Examples 1 to 3 and the results are shown in Table 5.

TABLE-US-00005 TABLE 5 Agent #2a Agent #1 m-xylylenediamine 31-706 Blend D Measured Viscosity (cP) 6 810 15 CaP Settings Cone 1, Cone 1, Cone 1, 2000 rpm 150 rpm 2000 rpm @ 25° C. @ 25° C. @ 25° C. Tg 2 by DSC 5 hrs @ 92 96.2 94.4 70° C. (° C.) DGEBA Liquid Epoxy (g) 126.9 118.4 125.2 Amine curing agent (g) 23.1 31.6 24.8 150 g TECAM Geltime @ 157 26 88.5 25° C. in a water bath (mins)

[0125] As for Examples 1 to 3, the curable epoxy resin/amine curing agent adhesive mixture was tested to measure, by differential scanning calorimetry (DSC), the Tg2 of the resultant cured epoxy resin adhesive after a period of 5 hours curing at an applied elevated curing temperature of 70° C. The measured Tg2 value is shown in Table 5.

[0126] Furthermore, the TECAM geltime at a temperature of 25° C. for the curable epoxy resin/amine curing agent adhesive mixture was measured as described above for Examples 1 to 3. The geltime is representative of the working time of the resin at ambient temperature.

[0127] Table 5 shows that Curing agent #2a exhibited a long geltime of 157 minutes. The geltime of Blend D was between the geltimes of Curing Agents #1 and #2a. In other words, adding Curing agent #2a to substitute for a portion of Curing Agent #1 increased the working time of the curable epoxy adhesive.

[0128] It may be seen unexpectedly that the Tg2 of the resin using Blend D, a 25:75 wt % mixture of Curing Agents #1 and #2a, is only slightly lower than the Tg2 of the resin using the Curing Agent #1. In other words, for this Blend D the mechanical properties of the cured epoxy resin are not reduced despite the increase in working time. This shows that adding a second amine curing agent, which is an aromatic diamine in accordance with this embodiment of the present invention, which is more latent than the base first amine curing agent can increase the working time without compromising the mechanical properties of the cured resin.

[0129] In further testing, as for Examples 1 to 3, the enthalpy of reaction was investigated for the resin formulations of Table 5.

[0130] Again, each value of exotherm temperature, and time taken to reach the peak exotherm temperature, was measured using the protocol of Examples 1 to 3, i.e. by curing in air at 70° C. a 10 mL sample, typically in a syringe of the curable epoxy resin adhesive composition.

[0131] The peak exotherm temperature and the time period to reach the peak exotherm temperature are listed in Table 6 for both Curing agent #2a and Blend D, as well as for Curing agent #1 which is the same data as in Table 3. Table 6 also lists the geltimes measured at 25° C. as specified above. The results for Curing agent #2a are also shown in FIG. 3 which shows the relationship between temperature and time during curing for for Curing agent #2a.

TABLE-US-00006 TABLE 6 Peak Exotherm Time To Peak Geltime @ Temperature Temperature 25° C. (° C.) (seconds) (minutes) Curing Agent #1 236.46 539 26 CURAMINE 31-706 Curing Agent #2a 238.71 940 157 m-xylylenediamine Blend D 272.16 790 88.5

[0132] FIG. 3 and Table 6 show that the latent system of Example 4, having a high (75 wt %) concentration of the m-xylylenediamine amine curing agent, i.e. Curing agent #2a, experienced only a slightly higher peak exotherm temperature than using the less latent CURAMINE 31-706 Curing agent #1. However, unexpectedly the present inventors have found that the peak exotherm temperature of Blend D is significantly higher than the peak exotherm temperature achievable by either of the individual Curing agent #1 and Curing agent #2a. This is unexpected, and the peak exotherm is high, giving good Tg2 values and mechanical properties, yet the geltime is long, giving a longer working time, without significantly increasing the curing time.

[0133] The present inventors therefore have again found unexpectedly that by using a more latent amine blend, a higher exotherm temperature can be realised during adhesive cure. Since the adhesive reactivity is proportional to temperature, the higher temperature to which the curable resin is exposed during cure will result in a faster cure rate and/or higher Tg of the resultant cured epoxy resin.

[0134] It can also be seen from FIG. 3 and Table 6 that the time period P3 from curing initiation to peak exotherm temperature for Blend D is 790 seconds measured when the curing is carried out in air at a curing temperature of 70° C. and on a resin sample having a volume of 10 mL which is cured in a syringe.

[0135] Tables 3 and 6 show that Blend D exhibited a higher peak exotherm temperatures than Blends A to C. The time to peak exotherm temperature for Blend D was only slightly higher than the time to peak exotherm temperature for Blend C, yet the geltime at 25° C. was significantly longer for Blend D than for Blend C. This data shows that the use of the aromatic diamine of Curing agent #2a can extend the working time as compared to the use of the aliphatic diamine of Curing agent #2, when each is combined with the base Curing Agent #1. The technical effect of the use of the aromatic diamine of Curing agent #2a, when combined with the base Curing Agent #1, is that the working time can be extended, even when the working is carried out at a temperature of 40° C., which is higher than the geltime test temperature of 25° C. The long working time at 40° C. can be achieved together with a high peak exotherm temperature, resulting in a high Tg2 and good mechanical properties, and a short cure time of typically 1-2 hours.

[0136] This shows that addition of the Curing agent #2a to the base Curing Agent #1 can achieve equivalent cure time, with the same or enhanced mechanical properties, yet with increased working time, even at an elevated working temperature of 40° C.

COMPARATIVE EXAMPLE 1

[0137] In this Comparative Example, the same epoxy resin was cured using a known amine curing agent, namely Jeffamine® D-230 available in commerce from Huntsman Advanced Materials. This known amine curing agent is a difunctional primary amine, in particular a polyoxypropylenediamine. The 10 ml syringe curing test of Table 3 and FIG. 3 was carried out and the results are shown in Table 3 and FIG. 3, together with the geltime.

[0138] It may be seen that the amine curing agent mixture used in accordance with the present invention can achieve a higher peak exotherm temperature, and at a significantly shorter time, than this known amine curing agent. This means that in practice the cure time can be reduced by up to 3 hours. The increased peak exotherm temperature can also increase the Tg2 of the resultant cured epoxy resin, and thereby achieve improved mechanical properties. In addition, the working time is longer for the amine curing agent mixture used in accordance with the present invention as compared to this known amine curing agent.

EXAMPLES 5 AND 6

[0139] In these Examples of a curable epoxy resin adhesive in accordance with the present invention, the epoxy resin component comprised an epoxy resin system and fillers/tougheners. The major (>50 wt %) component of the epoxy resin system was a diglycidyl ether bisphenol-A liquid epoxy resin (DGEBA) as used for the modelled epoxy resin system.

[0140] The curing agent component comprised an amine curing system, a reactive diluent adduct, and fillers/additives. In Example 5 the amine curing system comprised the Curamine 31-706 and Dytek A curing agents in the preferred 1:3 weight ratio as described above, i.e. comprising 4.7 wt % Curamine 31-706 and 14.1 wt % Dytek A. In Example 6 the amine curing system comprised the Curamine 31-706 and m-XDA curing agents in the preferred 1:3 weight ratio as described above, i.e. comprising 4.7 wt % Curamine 31-706 and 14.1 wt % m-XDA.

[0141] The geltime of the liquid components of the curable epoxy resin adhesive was measured at 25° C., and was found to be 149.3 minutes for Example 5 and 251.2 minutes for Example 6.

[0142] The curing properties of the curable epoxy resin adhesive, which as stated above included fillers/tougheners, were measured in a syringe having a volume of 60 mL using the test method described above for the 10 mL syringe.

[0143] At a curing temperature in an oven set at 30° C., the curable epoxy resin adhesive of Example 5 exhibited a peak exotherm of 107° C. after a time period of 97.2 minutes and the curable epoxy resin adhesive of Example 6 exhibited a peak exotherm of 59.2° C. after a time period of 123.2 minutes.

[0144] At a curing temperature in an oven set at 70° C., the curable epoxy resin adhesive of Example 5 exhibited a peak exotherm of 202.2° C. after a time period of 26.4 minutes and the curable epoxy resin adhesive of Example 6 exhibited a peak exotherm of 202.4° C. after a time period of 27.1 minutes.

[0145] These results are summarised in Table 7.

TABLE-US-00007 TABLE 7 Comparative Example 5 Example 6 Example 2 Geltime at 149.3 minutes 251.2 minutes 106.3 minutes 25° C. Peak exotherm 107° C. 59.2° C. 65.2° C. at 30° C. cure Time to peak 97.2 minutes 123.2 minutes 89.8 minutes exotherm at 30° C. cure Peak exotherm 202.2° C. 202.4° C. 185.9° C. at 70° C. cure Time to peak 26.4 minutes 27.1 minutes 25.7 minutes exotherm at 70° C. cure

[0146] The curable epoxy resin adhesive was cured in an oven at a curing temperature of 70° C. The oven was heated to the cure temperature from room temperature of 25° C. at a ramp rate of 1° C. per minute. The cure progression of the glass transition temperature Tg2 was measured by differential scanning calorimetry (DSC) at a ramp rate of 10° C. per minute and the results are set out in Table 8 for Examples 5 and 6.

TABLE-US-00008 TABLE 8 Example 5 Example 6 Cure time/temperature Tg2 - ° C. Tg2 - ° C. 60 minutes at 70° C. 47.4 63.1 90 minutes at 70° C. 66.9 Not measured 120 minutes at 70° C. 71.3 74.1 180 minutes at 70° C. 76.7 77.3 240 minutes at 70° C. Not measured 78.9 300 minutes at 70° C. Not measured 80.1

COMPARATIVE EXAMPLE 2

[0147] In Comparative Example 2, a known curable epoxy resin adhesive manufactured and sold by the Applicant was tested as for Example 5. This known curable epoxy resin adhesive comprises an epoxy resin component which is similar to that of Example 5, and the curing agent component comprises an amine curing agent system based upon a blend of polyether amines, isophorone diamine and amino ethyl piperizine.

[0148] The geltime and curing properties of the known adhesive were tested as for Example 5 and the results are summarised in Table 7.

[0149] A comparison of the results in Table 7, for both Examples 5 and 6, and Comparative Example 2, shows that the curable epoxy resin adhesive according to Examples 5 and 6 has a longer geltime at 25° C., a longer time to peak exotherm and a higher perk exotherm when cured at 30° C. and a slightly longer similar time to peak exotherm and a higher perk exotherm when cured at 70° C. as compared to the known curable epoxy resin adhesive of Comparative Example 2. In other words, the curable epoxy resin adhesive with according to the present invention has a longer working time and a similar cure time that the known adhesive. Since the peak exotherm is higher for the curable epoxy resin adhesive of Examples 5 and 6 as compared to the known curable epoxy resin adhesive of Comparative Example 2, the glass transition temperature Tg2 is higher for Examples 5 and 6 than for Comparative Example 2. Table 8 shows that at a cure temperature of 70° C. after a cure period of 180 minutes the glass transition temperature Tg2 for Example 5 is 76.7° C. and Example 6 is 77.3° C., and for Example 6 the Tg2 increases to 80.1° C. after a total cure period of 300 minutes (i.e. 5 hours). In contrast, the adhesive of Comparative Example 2 exhibits a glass transition temperature Tg1 of 72° C. after a period of 5 hours at a cure temperature of 70° C., and following an initial cure of 24 hours at 21° C.

[0150] Therefore the curable epoxy resin adhesive according to embodiments of the present invention can provide improved mechanical properties of the resultant cured adhesive.

[0151] Furthermore, a comparison of Examples 5 and 6 shows that the use of an aromatic diamine in Example 6 as compared to an aliphatic diamine in Example 6 can extend the working time, which can enable a long working time to be achieved at higher working temperatures such as 40° C., and can enable a higher Tg to be achieved without increasing the cure time.

[0152] Various modifications to the preferred embodiments of the present invention, as defined in the appended claims, will be apparent to those skilled in the art.