阅读说明：本技术 具有挤压垫片泡沫的拉挤成型件 (Pultruded part with extruded gasket foam ) 是由 亨利·E·理查森 于 2020-03-23 设计创作，主要内容包括：本发明大体上提供了一种包括拉挤型材和双组分体系的系统,该双组分体系的第一组分包含一种或多种环氧树脂,第二组分包含一种或多种磷酸酯,以便通过将第一组分与第二组分混合,形成在约0℃至约50℃的温度下活化的可活化材料。将该可活化材料挤出到所述拉挤型材上,使得该可活化材料被所述拉挤型材中由拉挤产生的余热活化。(The present invention generally provides a system comprising a pultruded profile and a two-component system having a first component comprising one or more epoxy resins and a second component comprising one or more phosphate esters such that upon mixing the first component with the second component, an activatable material is formed that is activated at a temperature of about 0 ℃ to about 50 ℃. Extruding the activatable material onto the pultruded profile such that the activatable material is activated by residual heat in the pultruded profile resulting from the pultrusion.)

1. A system, comprising:

a. pultrusion of the profile; and

b. a two-component system comprising:

i. a first component comprising one or more epoxy resins; and

a second component comprising one or more phosphate esters;

wherein the activatable material that is activated at a temperature of about 0 ℃ to about 50 ℃ is formed by mixing the first component with the second component.

2. The system of claim 1, wherein the activatable material is extruded onto the pultruded profile such that residual heat in the pultruded profile generated by pultrusion can activate the activatable material.

3. The system of claim 1, wherein the second component comprises three of the one or more phosphate esters.

4. A system as claimed in claim 1 or 2, wherein the one or more phosphate esters comprise a phosphate ester derived from cashew nut shell oil (CNSL).

5. The two-component system of any preceding claim, wherein the one or more phosphate esters comprise a phosphate ester derived from 2-ethylhexyl glycidyl ether.

6. The two-component system of any preceding claim, wherein the first component comprises one or more first-component additives.

7. The two-component system of claim 6, wherein the one or more first component additives comprise calcium carbonate, a mineral, a reinforcing fiber, hydrophobic silica, or any combination thereof.

8. The system of claim 7, wherein the calcium carbonate is present in an amount of about 15-25 w%.

9. The system of claims 7 and 8, wherein the calcium carbonate comprises ultrafine calcium carbonate, fine calcium carbonate, medium fine calcium carbonate, or any combination thereof.

10. The system of claims 7-9, wherein the first component comprises about 4-8 w% fine calcium carbonate and about 13-18 w% medium fine calcium carbonate.

11. The system of any preceding claim, wherein the second component comprises one or more second component additives.

12. The system of claim 8, wherein the one or more second component additives comprise a mineral, a reinforcing fiber, a hydrophobic silica, or any combination thereof.

13. The system of any preceding claim, wherein the one or more epoxy resins comprise one or more liquid epoxy resins, one or more flexible epoxy resins, one or more aliphatic multifunctional epoxy resins, one or more reactive diluents, or any combination thereof.

14. The system of claim 13, wherein the one or more liquid epoxy resins comprise a product of a reaction between epichlorohydrin and bisphenol a.

15. The system of claim 13 or 14, wherein the one or more liquid epoxy resins are present in an amount of about 6-10 w%.

16. The system of claims 13-15, wherein the one or more flexibilizing epoxy resins comprise a difunctional glycidyl ether epoxy resin, an unmodified BPA based epoxy resin, a multifunctional epoxidized polybutadiene resin, or any combination thereof.

17. The system of claims 13-16, wherein the one or more flexible epoxy resins are present in an amount of about 35-45 w%.

18. The system of claims 13-17, wherein the one or more aliphatic multifunctional epoxy resins comprises epoxidized sorbitol.

19. The system of claims 13-18, wherein the one or more aliphatic multi-functional epoxy resins are present in an amount of about 8-16 w%.

20. The two-component system of claims 13-19, wherein the one or more reactive diluents comprise polyethylene glycol diglycidyl ether and/or trimethylolethane triglycidyl ether.

21. The two-component system of claims 13-20, wherein the one or more reactive diluents are present in an amount of about 8-16 w%.

22. The system of any preceding claim, wherein the curing temperature is about 10 ℃ to 35 ℃.

23. The system of any preceding claim, wherein the curing temperature is about 15 ℃ to 25 ℃.

24. A system according to any preceding claim, wherein the curable composition has a cure time of from about 5 to about 15 min.

25. A system according to any preceding claim, wherein the curable composition has a cure time of from about 7 to 10 min.

26. The system of any preceding claim, wherein the volume expansion of the reaction product is from about 100% to about 800%.

27. The system of any preceding claim, wherein the reaction product has a volume expansion of about 400% to 500%.

28. The system of any preceding claim, wherein the curable composition is dispensed on a workpiece consisting of an automotive part.

29. A system according to any preceding claim, wherein the reaction product of the curable composition is a gasket.

30. The system of any preceding claim, wherein the composition is free of curing agents and/or curing accelerators.

31. A method, comprising:

a. pultrusion of one or more profiles through a pultrusion die;

b. mixing a two-component system comprising a first component comprising one or more epoxy resins and a second component comprising one or more phosphate esters to form an activatable material; and

c. extruding the activatable material onto the one or more profiles;

wherein the activatable material is extruded onto the one or more profiles exiting from the pultrusion die such that the activatable material is activatable by residual heat in the one or more profiles resulting from pultrusion.

32. The method of claim 31, wherein the second component comprises three different phosphate esters.

33. The method of claim 31 or 32, wherein the first component comprises one or more first component additives.

34. The method of claim 31 or 33, wherein the second component comprises one or more second component additives.

35. The method of claim 31 or 34, wherein the one or more first component additives comprise calcium carbonate.

36. The method of claim 31, wherein curing occurs at a temperature of about 10 ℃ to about 35 ℃.

37. The method of claim 31, wherein curing occurs at a temperature of about 15 ℃ to about 25 ℃.

38. The method of claim 31, wherein the activatable material has a cure time of about 5 to 15 minutes.

39. The method of claim 31, wherein the activatable material has a cure time of about 7-10 min.

40. The method of claim 31, wherein the activatable material has a volume expansion of about 100% to about 800%.

41. The method of claim 31, wherein the volume expansion of the reaction product of the activatable material is from about 400% to about 500%.

42. The method of claim 31, wherein the activatable material is dispensed on the one or more profiles, the one or more profiles being one or more automotive components.

43. The method of claim 31, wherein the activatable material is a gasket.

44. The method of claim 31, wherein the composition is free of curing agents and/or curing accelerators.

Technical Field

The present invention generally relates to a pultrudate having an extruded gasket foam that is curable at room temperature. The extruded gasket may generally comprise a composition consisting of a first component and a second component. More particularly, the present invention relates to gasket materials based on epoxy resins and phosphate esters.

Background

Gasket materials are often used for a variety of purposes in the transportation and construction industries. For example, the gasket material may serve one or more of structural support, sealing, and sound attenuation.

Die-cut gasket materials have been used in various industries, particularly in the transportation and construction industries. Typically, die cut gasket materials include a foam that is applied to the workpiece after molding and may be adhered to the workpiece by an adhesive (e.g., a pressure sensitive adhesive). Some of the disadvantages of die-cut gasket materials include the additional labor and process resources inherent in the die-cutting process, the waste generated by the die-cutting, and the separate adhesives required.

The foaming reaction in place allows for dispensing of the gasket material directly onto the workpiece. Polyurethane-based foams are most commonly used where room temperature activation (e.g., expansion) is desired. Polyurethane foams have a number of disadvantages, such as the presence of isocyanates, limited adhesion to certain substrates, poor hydrolysis resistance in humid environments, unsuitability for slower-reacting systems, high sensitivity to temperature changes during distribution and foaming, and the need for highly specific mixing ratios in the formulation.

As an alternative to polyurethane-based foams, phosphoric acid has been used to perform in situ foaming reactions in polymeric materials. However, phosphoric acid causes other problems. For example, the reaction time with phosphoric acid is very fast, which is not ideal for assembly processes that require time to position the polymeric material onto the surface prior to foaming. Therefore, a slight delay in reaction time may be preferable. In some cases, the nature of phosphoric acid may pose negative health and safety concerns. Therefore, alternative materials that are healthy and have a lower safety risk may be preferred. Phosphoric acid also has a significant difference in viscosity from polymeric materials. This presents challenges to the manufacture (e.g., mixing) and storage of the materials. Phosphoric acid also has a much smaller molecular weight than many polymeric materials, thereby resulting in an undesirable mixing ratio. It is preferred to use a relatively close mixing ratio of 1:1 or 2: 1. Finally, the reactivity of phosphoric acid makes it difficult to use in formulating adhesive and sealant materials, as many chemical components may be unstable when used with phosphoric acid. Preferably, the polymer can contain various moieties that may facilitate adhesion, physical or chemical compatibility, and the like.

International patent publication No. WO 2016/149700 a1 (incorporated herein by reference for all purposes) discloses the use of phosphate esters as a replacement for phosphoric acid.

Despite the above efforts, there remains a need for improved gasket materials. There is a need for gasket materials that can be cured at room temperature. There is a need for gasket materials that are capable of expanding and crosslinking at low temperatures compared to known gasket materials. A gasket material capable of adhering to a variety of substrates is needed. It is desirable that the gasket material utilize components that are both curable and foamable without the need for additional components. It is desirable that the gasket material have the desired fire, smoke and gas protection (FST) characteristics without the need for other agents to impart these characteristics.

Summary of The Invention

The present invention provides one or more of the above-described benefits. The gasket material of the present invention may be used for one or more of the following purposes: cavity filling, sealing, reinforcement or damping. The gasket material may be extruded. The gasket material may be extruded onto the pultrusion.

The present invention provides a pultruded profile having an activatable material disposed thereon, the activatable material comprising a two-component system comprising a first component comprising one or more epoxy resins; and a second component comprising one or more phosphate esters; wherein, after mixing the first and second components to form a curable composition, the curable composition is cured at a temperature of about 0 ℃ to about 50 ℃.

The present invention can provide an activatable material comprising a two-component system comprising a first component comprising one or more liquid epoxy resins, one or more flexible epoxy resins, an aliphatic multi-functional epoxy resin, one or more reactive diluents, and one or more first component additives, and a second component comprising a first phosphate ester, a second phosphate ester, a third phosphate ester, and one or more second component additives; wherein, after mixing the first and second components to form a curable composition, the curable composition is cured at a temperature of about 0 ℃ to about 50 ℃; wherein the activatable material is a shim foam that is extruded onto the pultruded profile.

The second component of the activatable material may comprise three of the one or more phosphate esters.

The second component of the activatable material may comprise three of the one or more phosphate esters. The one or more phosphate esters may include a phosphate ester derived from cashew nut shell oil (CNSL). The one or more phosphate esters may include a phosphate ester derived from 2-ethylhexyl glycidyl ether.

The first component of the activatable material may comprise one or more first component additives. The one or more first component additives may include calcium carbonate, minerals, reinforcing fibers, hydrophobic silica, or any combination thereof. The calcium carbonate may be present in an amount of about 15-25 w%. The calcium carbonate may include ultrafine calcium carbonate, fine calcium carbonate, medium fine calcium carbonate, or any combination thereof. The first component may comprise about 4-8% by weight fine calcium carbonate and about 13-18% by weight medium fine calcium carbonate. The composition of any of the preceding claims, wherein the second component may comprise one or more second component additives. The one or more second component additives may include calcium carbonate, minerals, reinforcing fibers, hydrophobic silica, or any combination thereof.

The one or more epoxy resins may include one or more liquid epoxy resins, one or more flexible epoxy resins, one or more aliphatic multifunctional epoxy resins, one or more reactive diluents, or any combination thereof. The one or more liquid epoxy resins may include the product of a reaction between epichlorohydrin and bisphenol a. The one or more liquid epoxy resins may be present in an amount of about 6-10 w%. The one or more flexible epoxy resins can include a difunctional glycidyl ether epoxy resin, an unmodified BPA based epoxy resin, a multifunctional epoxidized polybutadiene resin, or any combination thereof. The one or more flexible epoxy resins may be present in an amount of about 35-45 w%. The one or more aliphatic multifunctional epoxy resins may include epoxidized sorbitol. The one or more aliphatic multi-functional epoxy resins may be present in an amount of about 8-16% by weight. The one or more reactive diluents may include polyethylene glycol diglycidyl ether and/or trimethylolethane triglycidyl ether. The one or more reactive diluents may be present in an amount of about 8-16% w.

The activatable material may be activated at a temperature of from about 10 ℃ to about 35 ℃. The activation temperature may be about 15 ℃ to 25 ℃. Upon activation, the activatable material may cure, foam, expand, seal, adhere, or a combination thereof. The activation time of the activatable material may be about 5-15 min. The activation time of the activatable material may be about 7-10 min. The volume expansion of the resulting reaction product may be about 100% to 800%. The volume expansion of the resulting reaction product may be about 400% to 500%.

The activatable composition may be dispensed onto a workpiece comprised of an automotive part. The workpiece may be a pultruded profile. The reaction product of the activatable material may be a gasket. The two-component system of activatable material may be free of curing agents and/or curing accelerators. Activation of the activatable material may be triggered by residual heat in the pultruded profile.

A method, comprising: drawing and extruding a profile, extruding an activatable material having a two-component system onto the profile, and activating the activatable material on the profile, wherein the two-component system comprises a first component and a second component, and the first component comprises one or more epoxy resins and the second component comprises one or more phosphate esters; mixing the first component and the second component to produce a reaction product, and wherein the first component and the second component are mixed to produce an activatable material; the activatable material is activated at a temperature of about 0 ℃ to about 50 ℃, and wherein the activatable material is activated by residual heat in the profile produced by the pultrusion process.

The second component of the two-component system may comprise three different phosphate esters. The first component of the two-component system may comprise one or more first component additives. The second component may comprise one or more second component additives. The one or more first component additives may include calcium carbonate.

Activation may occur at a temperature of from about 10 ℃ to about 35 ℃. Activation may occur at a temperature of about 15 ℃ to about 25 ℃. The curing time of the activatable material may be about 5-15 min. The curing time of the activatable material may be about 7-10 min. The volume expansion of the activatable material may be from about 100% to about 800%. The volume expansion of the reaction product may be about 400% to 500%.

The activatable material may be dispensed on a workpiece comprised of an automotive part. The reaction product of the activatable material may be a gasket. The activatable material may be free of curing agents and/or curing accelerators.

Drawings

FIG. 1 is a perspective view of a pultruded component with extruded gasket foam;

FIG. 2 is another view of a pultruded component with extruded shim foam.

Detailed Description

The present invention meets one or more of the above-described needs by improving compositions and methods described herein. The description and illustrations presented herein are intended to acquaint others skilled in the art with the invention and its principles and practical application. Those skilled in the art may adapt and apply the invention in its numerous forms, as may be required by the particular use contemplated. Accordingly, the particular embodiments of the invention as set forth are not intended to be exhaustive or limiting of the invention. The scope of the invention should, therefore, be determined not with reference to the above description, but instead should be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled. The disclosures of all articles and references, including patent applications and publications, are incorporated herein by reference for all purposes. Other combinations are possible, as derived from the following claims, which are also incorporated by reference into this written description.

The present invention provides an activatable material that can be configured for use with a pultrusion. The activatable material may be activated by a selected stimulus. For example, the activatable material may be heat activated at a temperature of from about 0 ℃ to about 50 ℃. The activatable material may be extruded onto the pultrusion. The pultruded element may be a pultruded profile for use as an automotive component. The pultruded profile may retain some of the residual heat from the pultrusion process, which may then be used to activate the activatable material as it is extruded onto the profile.

The present invention provides an activatable material which may be a two-component composition consisting of an a-side (i.e., the first component) and a B-side (i.e., the second component). The two-component composition, upon mixing, can form an activatable material and, upon activation, can form a reaction product, which can be a gasket material.

The a-side may comprise one or more epoxy resins, one or more additives, and/or one or more monomers. The one or more epoxy resins may include one or more liquid epoxy resins, one or more flexible epoxy resins, one or more epoxy novolac resins, one or more aliphatic multifunctional epoxy resins, one or more reactive diluents, one or more phenoxy resins, one or more silane modified epoxy resins, one or more surfactants, one or more monomers, or any combination thereof. The one or more additives may include one or more toughening agents (e.g., core shell polymers), calcium carbonate, minerals, reinforcing fibers, hydrophobic silica, platy alumina, or any combination thereof.

The B-side may comprise one or more phosphate esters, phosphoric acid, one or more additives, one or more surfactants, one or more monomers, or any combination thereof. The one or more phosphate esters can include a first phosphate ester, a second phosphate ester, a third phosphate ester, or any combination thereof. The one or more additives may include one or more toughening agents (e.g., core shell polymers), minerals, reinforcing fibers, hydrophobic silica, platy alumina, or any combination thereof.

The one or more phosphate esters may be formed by reaction between phosphoric acid and various alcohols. The one or more phosphate esters may be formed by reaction between phosphoric acid and the epoxy groups of a phosphate ester precursor (i.e., a component that has not been reacted with phosphoric acid). The one or more phosphate esters may be reacted with CNSL (e.g., under the trade name phosphoric acid)CNSL sold by LITE 2513HP, commercially available from Cardolite corporation of Monmouth Junction, new jersey). The one or more phosphate esters may be prepared by reacting phosphoric acid with phenyl glycidyl ether (e.g., under the trade name phenyl glycidyl ether)Phenyl glycidyl ether sold by GE-13, commercially available from CVC Thermoset Specialties, Mooretown, N.J.). The phosphate ester may be prepared by reacting phosphoric acid with 2-ethylhexyl glycidyl ether (e.g., under the trade name phosphoric acid ester)2-ethylhexyl glycidyl ether sold by GE-6, commercially available from CVC Thermoset Specialties, Mooretown, N.J.). The one or more phosphate esters may be prepared by reacting phosphoric acid with epoxidized p-tert-butylphenol (e.g., under the trade nameEpoxidized p-tert-butylphenol sold by GE-11, commercially available from CVC Thermoset Specialties, Mooretown, N.J.).

The CNSL may contain chemicals typically extracted from CNSL including anacardic acid, cardanol, or any combination thereof. Preferably, the glycidyl ether of CNSL is the glycidyl ether of cardanol.

The one or more phosphate esters may be selected from mono-, di-, or tri-esters as shown below:

the one or more phosphate esters may be obtained from the reaction between an epoxy group and phosphoric acid, as shown below:

the B side may comprise one or more phosphate esters and/or one or more phosphate ester precursors. The B-side may comprise one or more phosphate ester precursors, which may be combined with the phosphoric acid prior to combination with the a-side. The B-side may comprise one or more phosphate esters, which may be pre-reacted (i.e., reacted between the phosphate ester and the epoxide) prior to addition to the B-side.

The first phosphate ester may be phosphoric acid and CNSL (e.g., under the trade name of CNSL)CNSL sold by LITE 2513HP as commercially available from Cardolite corporation of Monmouth Junction, N.J.). The second phosphate ester may be phosphoric acid and 2-ethylhexyl glycidyl ether (e.g., under the trade name phosphoric acid and phosphoric acid)2-ethylhexyl glycidyl ether sold by GE-6, commercially available from CVC Thermoset Specialties, Mooretown, N.J.).

The first phosphate ester may be present in an amount of about 20-45 w% of the B side. The first phosphate ester may be present in an amount of about 25-35 w% of the B side. The first phosphate ester may be present in an amount of about 28-32 w% of the B side. The first phosphate ester may be present in an amount of about 32 w% of the B side. The second phosphate ester may be present in an amount of about 10-30 w% of the B side. The second phosphate ester may be present in an amount of about 15-25 w% of the B side. The second phosphate ester may be present in an amount of about 18-22 w% of the B side. The second phosphate ester may be present in an amount of about 21 w% of the B side. The third phosphate ester may be present in an amount of about 30-65 w% of the B side. The third phosphate ester may be present in an amount of about 35-45 w% of the B side. The third phosphate ester may be present in an amount of about 42 w% of the B side. The third phosphate ester may be present in an amount of about 58 w% of the B side. The third phosphate ester may be present in an amount of about 60 w% of the B side.

The first phosphate ester and the third phosphate ester may be present without the second phosphate ester. The first phosphate ester may be present in an amount of about 25-35 w% of the B side. The first phosphate ester may be present in an amount of about 30 w% of the B side. The third phosphate ester may be present in an amount of about 55-65 w% of the B side. The third phosphate ester may be present in an amount of about 60 w% of the B side.

The B side may comprise phosphoric acid. The phosphoric acid may be orthophosphoric acid and/or polyphosphoric acid. The phosphoric acid may be polyphosphoric acid. The phosphoric acid may be the free acid in the one or more phosphate esters, and/or may be added independently of the one or more phosphate esters. The addition of phosphoric acid to the B-side can result in more expansion (e.g., foaming) of the resulting reaction product. When the temperature is below 23 ℃, the addition of phosphoric acid to the B-side can enhance the reactivity of the two-component system to help maintain the desired level of expansion and/or cure.

The independently added phosphoric acid may be present in the aqueous solution in an amount of 85% or more, or even 95% or more (i.e., reagent grade phosphoric acid). The independently added phosphoric acid may be present in an amount of about 1-10 w% of the B side. The independently added phosphoric acid may be present in an amount of about 2-6 w% of the B side. The independently added phosphoric acid may be present in an amount of about 4 w% of the B side.

The one or more phosphate esters formed from the reaction of phosphoric acid and the epoxy-containing component may comprise free acid. The free acid content of the one or more phosphate esters may be about 1% or more, 3% or more, 5% or more, 15% or less, 13% or less, or even 11% or less.

After addition of the a-side and B-side, the two-component system can foam due to the reaction between the metal carbonate or metal bicarbonate and the acid, thereby releasing gas (i.e., chemical expansion occurs). This reaction mechanism is described in U.S. patent No. 5,648,401, which is incorporated herein by reference for all purposes.

Curing, foaming, expanding, sealing, adhering, or a combination thereof may occur at a temperature of about 50 ℃ or less, about 40 ℃ or less, about 30 ℃ or less, about 20 ℃ or less, about 0 ℃ or more, or even about 10 ℃ or more. Curing, foaming, expanding, sealing, adhering, or a combination thereof may occur at a temperature of about 10 ℃ to about 35 ℃. Curing, foaming, expanding, sealing, adhering, or a combination thereof may occur at a temperature of about 10 ℃. Curing, foaming, expanding, sealing, adhering, or a combination thereof may occur at room temperature (e.g., a temperature of about 15 ℃ to about 25 ℃). Curing, foaming, expanding, sealing, adhering, or a combination thereof may occur at a temperature of about 23 ℃.

The present invention contemplates a relatively fast activation time compared to other activatable materials or curing systems without the addition of a stimulus (e.g., at room temperature). The activation time of the reaction product may be 75min or less, 50min or less, 30min or less, 20min or less. The activation time may be about 2min or longer, 8min or longer, and even 16min or longer. The activation time of the resulting reaction product may be about 5-20 min. The activation time of the resulting reaction product may be about 10 min. The activation time of the resulting reaction product may be about 7 min. The activation time of the resulting reaction product may be about 5 min.

Foaming may begin before the resulting reaction product is fully cured. The foaming time of the reaction product (i.e., the time frame for effective foaming of the two-component system) can be 30min or less, or even 20min or less. The foaming time of the reaction product may be about 1 to 10 min. The activation time of the reaction product may be about 5 min. The activation time of the reaction product may be about 7 min.

The a-side may comprise one or more epoxy-based materials (i.e., one or more epoxy resins). The one or more epoxy resins may be any conventional dimeric, oligomeric or polymeric epoxy resin. The one or more epoxy resins may contain at least one epoxy functional group (i.e., a monofunctional epoxy resin), or may contain more than one epoxy functional group (i.e., a multifunctional epoxy resin). The one or more epoxy resins may contain one or more, two or more, three or more, or even four or more epoxy functional groups. The one or more epoxy resins may be modified epoxy resins (e.g., silane-modified, elastomer-modified, etc.). The one or more epoxy resins may be aliphatic, cycloaliphatic, aromatic, and the like epoxy resins, or any combination thereof. The one or more epoxy resins may be present as a solid (e.g., in the form of granules, blocks, pieces, etc., or any combination thereof) or a liquid (e.g., a liquid epoxy resin). As used herein, an epoxy resin is a solid resin if it is solid at a temperature of 23 ℃; if the epoxy resin is liquid at a temperature of 23 ℃, it is a liquid resin unless otherwise specified. The one or more epoxy resins may include one or more liquid epoxy resins, one or more flexible epoxy resins, one or more epoxy novolac resins, one or more aliphatic multifunctional epoxy resins, one or more reactive diluents, one or more phenoxy resins, one or more silane modified epoxy resins, or any combination thereof.

The two-component system may comprise one or more liquid epoxy resins. The one or more liquid epoxy resins may be used as a binder for the epoxy resin component. The one or more liquid epoxy resins may be the product of a reaction between epichlorohydrin (hereinafter referred to as EPH) and any conventional bisphenol. The one or more liquid epoxy resins may be the product of a reaction between EPH and bisphenol A (hereinafter BPA) and/or bisphenol F (hereinafter BPF). Measurements made according to ASTM D1652-97 show that the one or more liquid epoxy resins can have an epoxy equivalent weight (hereinafter EEW) of about 160-192 g/eq. The one or more liquid epoxy resins may have an epoxy percentage of about 20 to about 25. Measurements made according to ASTM D445 indicate that the viscosity of the one or more liquid epoxy resins at a temperature of 25 ℃ may be about 2,000-14,000 cP. Suitable BPA-based liquidsAn example of an epoxy resin may be d.e.r available from Dow Chemical company (Midland, missouri).^TM331. An example of a suitable BPF-based liquid epoxy resin may be YDF-170, available from Kukdo Chemical company (Korea).

The one or more liquid epoxy resins may be present as part of the a-side. The one or more liquid epoxy resins may be present in an amount of about 4-15 w% of the a-side. The one or more liquid epoxy resins may be present in an amount of about 6-10 w% of the a-side. The one or more liquid epoxy resins may be present in an amount of about 8 w% of the a-side.

The two-component system may comprise one or more flexible epoxy resins. The one or more flexible epoxy resins may act on the reaction product as follows: decreasing the compressive modulus, increasing the strain to failure, decreasing the recovery time, increasing the crosslink density in the reaction product, increasing the impact resistance, improving the adhesion, increasing the chemical resistance, or any combination thereof. The one or more flexible epoxy resins may act as a viscosity modifier to increase the gas entrapment capability of the two-component system. The one or more flexible epoxy resins can be a difunctional glycidyl ether epoxy resin, an unmodified BPA based epoxy resin, a multifunctional epoxidized polybutadiene resin, or any combination thereof. Measurements made according to ASTM D1652-97 show that the EEW of the one or more flexible epoxy resins can be about 260-500. Measurements made according to ASTM D445 indicate that the one or more flexible epoxy resins may have a viscosity of about 700-25,000cP at a temperature of 25 ℃. Examples of suitable flexible epoxy resins may include NC-514 (available from Cardolite corporation of Monmouth Junction, N.J.), (R),PY 4122 (available from Huntsman Advanced Materials, Inc. of salt lake City, Utah), Poly605E (available from Cray Valley, Exton, pa), or any combination thereof.

The one or more flexible epoxies may be present on the a-side. The one or more flexible epoxy resins may be present in an amount of about 30-50 w% of the a-side. The one or more flexible epoxy resins may be present in an amount of about 35-45 w% of the a-side. The one or more flexible epoxy resins may be present in an amount of about 39 w% of the a-side. The one or more flexibilizing epoxy resins may include about 10-18% by weight of the A-side difunctional glycidyl ether epoxy resin, about 8-16% by weight of the A-side unmodified BPA-based epoxy resin, and about 8-16% by weight of the A-side multifunctional epoxidized polybutadiene resin. The one or more flexible epoxy resins may include about 14% by weight of the A-side difunctional glycidyl ether epoxy resin, about 12% by weight of the A-side unmodified BPA-based epoxy resin, and about 12% by weight of the A-side multifunctional epoxidized polybutadiene resin. The two-component system may comprise difunctional glycidyl ether epoxy resin, difunctional epoxy resin derived from cardanol, and multifunctional epoxidized polybutadiene resin, respectively, in a ratio of about 1:1: 1. The two-component system may comprise difunctional glycidyl ether epoxy resin, difunctional epoxy resin derived from cardanol, and multifunctional epoxidized polybutadiene resin, respectively, in a ratio of about 1:0.8: 0.8. The two-component system may comprise difunctional glycidyl ether epoxy resin, difunctional epoxy resin derived from cardanol, and multifunctional epoxidized polybutadiene resin, respectively, in a ratio of about 1:0.9: 0.9.

The two-component system described herein may also comprise one or more epoxy novolac resins. The one or more epoxy novolac resins can impart chemical resistance, solvent resistance, temperature resistance, or any combination thereof to the reaction product. The one or more epoxy novolac resins may be present as part of the a-side. Measurements made according to ASTM D1652-97 show that the EEW of the one or more epoxy novolac resins can be about 165-183 g/eq. The one or more epoxy novolac resins may have an average epoxy functionality of about 2.6 to about 6.5. Measurements made according to ASTM D445 indicate that the one or more epoxy novolac resins may have a viscosity of about 18,000-30,000cP at a temperature of 25 ℃. Examples of suitable epoxy novolac resins are available under the trade names Epalloy 8250 and Epalloy 8330, which are available from CVC Thermoset Specialties, Inc. (Mooretown, N.J.).

The one or more epoxy novolac resins may be present in an amount of about 30-50 w% of the a-side. The one or more epoxy novolac resins may be present in an amount of about 35-45 w% of the a-side. The one or more epoxy novolac resins may be present in an amount of about 38-42 w% of the a-side. The one or more epoxy novolac resins may be present in an amount of about 42 w% of the a-side. The one or more epoxy novolac resins may include an epoxy novolac resin having a functionality of about 3.6 (about 10-18 w% of the a-side), and an epoxy novolac resin having a functionality of about 6.5 (about 22-32 w% of the a-side). The one or more epoxy novolac resins may include an epoxy novolac resin having a functionality of about 3.6 (about 15 w% of the a-side), and an epoxy novolac resin having a functionality of about 6.5 (about 28 w% of the a-side). The two-component system may comprise an epoxy novolac resin having a functionality of about 3.6 and an epoxy novolac resin having a functionality of about 6.5 in a ratio of about 1:2 to about 1: 3.

The two-component system may comprise one or more aliphatic multifunctional epoxy resins. The one or more aliphatic multifunctional epoxy resins may function to increase the degree of crosslinking and/or enhance the chemical resistance of the reaction product. The one or more aliphatic multifunctional epoxy resins may include epoxidized sorbitol. Measurements made according to ASTM D1652-97 show that the EEW of the one or more aliphatic multi-functional epoxy resins can be about 160-195 grams/equivalent. Measurements according to ASTM D445 indicate that the one or more aliphatic multifunctional epoxy resins may have a viscosity of about 4,000-18,000cP at a temperature of 25 ℃. Examples of suitable aliphatic multifunctional epoxy resins may be available under the trade nameGE-60 andaliphatic multifunctional epoxy resins sold by GE-61 and available from CVC Thermoset Specialties, Inc. (Moorest, N.J.)own) was purchased.

The one or more aliphatic multifunctional epoxy resins may be present as part of the a-side. The one or more aliphatic multi-functional epoxy resins may be present in an amount of about 5-20 w% of the A-side. The one or more aliphatic multi-functional epoxy resins may be present in an amount of about 8-16 w% of the A-side. The one or more aliphatic multi-functional epoxy resins may be present in an amount of about 10-14 w% of the A-side. The one or more aliphatic multi-functional epoxy resins may be present in an amount of about 12 w% of the a-side.

The two-component system may comprise one or more reactive diluents. The one or more reactive diluents may function to reduce the overall viscosity of the two-component system, to adjust the flow conditions of the two-component system during or after dispensing on a workpiece, and/or to increase the degree of crosslinking of the reaction product. The one or more reactive diluents may be polymeric diluents, thereby increasing the flexibility of the reaction product; and/or the one or more reactive diluents may be multifunctional diluents, thereby promoting crosslinking and imparting chemical resistance to the reaction product. The one or more reactive diluents may include polyethylene glycol diglycidyl ether and/or trimethylolethane triglycidyl ether. Measurements made according to ASTM D1652-97 show that the EEW of the one or more reactive diluents can be about 150-170 g/eq. Measurements made according to ASTM D445 indicate that the viscosity of the one or more reactive diluents may be about 200-300cP at a temperature of 25 ℃. Examples of suitable reactive diluents may be under the trade nameGE-31 andreactive diluents sold by GE-24, commercially available from CVC Thermoset Specialties, Inc. (Mooretown, N.J.).

The one or more reactive diluents may be present in an amount of about 5-20 w% of the a side. The one or more reactive diluents may be present in an amount of about 8-16 w% of the a side. The one or more reactive diluents may be present in an amount of about 10-14 w% of the a-side. The one or more reactive diluents may be present in an amount of about 13 w% of the a side. The one or more reactive diluents may include about 2-6% by weight of polyethylene glycol diglycidyl ether on the A-side, and about 6-14% by weight of trimethylolethane triglycidyl ether on the A-side. The one or more reactive diluents may include about 4% w polyethylene glycol diglycidyl ether on the a-side and about 9% w trimethylolethane triglycidyl ether on the a-side. The two-component system may comprise polyethylene glycol diglycidyl ether and trimethylolethane triglycidyl ether, respectively, in a ratio of about 1:2 to 1: 3.

The two-component system may comprise one or more phenoxy resins (i.e. polyhydroxy ethers). The one or more phenoxy resins may provide the reaction product with greater adhesion, corrosion resistance, heat resistance, or any combination thereof. The one or more phenoxy resins are obtainable by the reaction between BPA and EPH. The one or more phenoxy resins may have terminal hydroxyl groups and hydroxyl groups in each repeating polymeric unit. Measurements made according to ASTM D1652-97 show that the EEW of the phenoxy resin or resins can be about 202-214 g/eq. Measurements made according to ASTM D445 indicate that the one or more phenoxy resins may have a viscosity of about 20,000-50,000cP at a temperature of 25 ℃. An example of a suitable Phenoxy resin may be Phenoxy LER-HB available from Gabriel Chemical company (Akron, Ohio).

The one or more phenoxy resins may be present in an amount of about 5-15 w% of the a side. The one or more phenoxy resins may be present in an amount of about 5-15 w% of the a side. The one or more phenoxy resins may be present in an amount of about 10 w% of the a side.

The two-component system may comprise one or more silane-modified epoxy resins. The one or more silane-modified epoxy resins may provide the reaction product with improved adhesion, particularly to glass and/or metal. Examples of suitable silane-modified epoxy resins may be available under the trade nameKSR-177, a commercially available silane-modified epoxy resin available from Kukdo Chemical company (Korea).

The one or more silane-modified epoxy resins may be present on the a-side. The one or more silane-modified epoxy resins may be present in an amount of about 1-7 w% of the A-side. The one or more silane-modified epoxy resins may be present in an amount of about 2-6 w% of the A-side. The one or more silane-modified epoxy resins may be present in an amount of about 4 w% of the a-side.

The two-component system may comprise one or more surfactants. The one or more surfactants may act as emulsifiers. The one or more surfactants can comprise a hydrophobic portion and a hydrophilic portion. The one or more surfactants may have an acid number of about 85 to about 100 when measured at a pH of about 5.5 and an acid number of about 160 to about 180 when measured at a pH of about 9.5. Measurements made according to ASTM D445 indicate that the viscosity of the one or more surfactants at a temperature of 25 ℃ can be about 32,500-42,500 cP. The one or more surfactants may be nonylphenol ethoxylated phosphate esters in which the nonyl moiety is a hydrophobic moiety and the ethoxylated phosphate ester moiety is a hydrophilic moiety. An example of a suitable surfactant may be available under the trade name Dextrol^TMOC-110, a surfactant commercially available from Ashland, Inc. (Covington, Kentucky).

The one or more surfactants may be present on the B-side. The one or more surfactants may be present in an amount of about 6-18 w% of the B-side. The one or more surfactants may be present in an amount of about 8-16 w% of the B-side. The one or more surfactants may be present in an amount of about 10-14 w% of the B-side. The one or more surfactants may be present in an amount of about 12 w% of the B-side.

The two-component system may comprise one or more monomers. The one or more monomers can be used to improve the adhesion properties of the reaction product (particularly to a metal substrate), increase the flexibility of the reaction product, increase the impact resistance of the reaction product, or any combination thereof. The monomer or monomers may have mono-, di-or even multi-functional groups. The one or more monomers may be the product of an esterification reaction between an alcohol and acrylic or methacrylic acid. The one or more monomers may be monofunctional acrylic monomers. Preferably, the one or more monomers may be a mixture of methacrylate and ethyl 2- (2-ethoxyethoxy) acrylate. Examples of suitable monomers may be those sold under the trade name SR 9050, available from Sartomer corporation (Exton, Pa.).

The two-component system may comprise one or more monomers in the a-side and/or the B-side. The one or more monomers may be present in an amount of about 10-26 w% of the A-side and/or B-side. The one or more monomers may be present in an amount of about 12-24 w% of the A-side and/or B-side. The one or more monomers may be present in an amount of about 14-22 w% of the A-side and/or B-side. The one or more monomers may be present in an amount of about 18 w% of the a-side and/or B-side.

The cure rate and/or degree of crosslinking may be a function of the functionality of the two-component system (a-side and B-side). If the pre-polymerized component in a two-component system has a shorter polymer length (i.e., a higher melt flow index MFI), the two-component system may require a higher functionality (i.e., the number of functional groups on one or more of the polymerizable components); thus, the structural backbone deficiency caused by shorter polymers can be compensated by a higher degree of crosslinking. If the pre-polymerized component in a two-component system has a longer polymer length (i.e. a lower MFI), the two-component system may require a lower functionality; thus, more structural backbone is produced from longer polymers, thereby eliminating the need for high functionality.

The B side can be at least partially formed as a salt by utilizing at least some phosphoric acid and phosphate ester, thereby reducing the functionality of the B side. The a-side may contain a higher functionality component to compensate for the reduced functionality of the B-side. By creating a polymer matrix with functionality higher than 2, the a-side with higher functionality can be formulated.

The two-component system may comprise one or more additives. The one or more additives may include one or more toughening agents, calcium carbonate, minerals, reinforcing fibers, hydrophobic silica, platy alumina, or any combination thereof.

The two-component system may comprise one or more toughening agents. The one or more toughening agents may be used to distribute energy (i.e., increase impact resistance) within the reaction product. The one or more toughening agents may help to improve T-peel strength. The one or more toughening agents may include thermoplastics, thermosets or thermosettable plastics, elastomers, and the like, or any combination thereof. The one or more toughening agents may comprise an elastomer (including elastomer-containing materials) and/or a core shell polymer (which may include, but is not limited to, an elastomer).

The core-shell polymer may include a first polymeric material (i.e., a core material) and a second polymeric material (i.e., a shell material). The first polymeric material may be completely encapsulated by the second polymeric material. The core shell polymer may comprise about 30 w% or more, 50 w% or more, even 70 w% or more of the first polymeric material. The first polymeric material and/or the second polymeric material can comprise one, two, three, or even more polymers that are combined and/or reacted together (e.g., sequentially polymerized), or can be part of different or the same core shell polymer system. An example of a suitable core shell polymer may be that sold under the trade name Kane Ace^TMMX-267, a core shell polymer available from Kaneka North America, Inc. (Pasadena, Tex.).

The core shell polymer may be present in an amount of about 1-10 w% of the a-side and/or the B-side (e.g., if the core shell polymer is present in an amount of 10 w%, it may be present in an amount of 5 w% in the a-side and 5 w% in the B-side). The core shell polymer may be present in an amount of about 2 to 8 w% of the A-side and/or B-side. The core shell polymer may be present in an amount of about 4-6 w% of the A-side and/or B-side. The core shell polymer may be present in an amount of about 5 w% of the a-side and/or B-side.

The two-component system may comprise one or more metal carbonates. The one or more metal carbonates can be used to generate gas in the presence of an acid, as a filler, to control the start and/or overall extent of the foaming (e.g., expansion) process. The one or more metal carbonates can be metal carbonates or metal bicarbonates. Examples of suitable fillers may include calcium carbonate, nickel carbonate, barium carbonate, sodium bicarbonate, and potassium bicarbonate. Preferably, the one or more metal carbonates may include calcium carbonate. The expansion and solidification of the two-component system can be controlled by the particle size of the metal carbonate and/or metal bicarbonate, whereby the total surface area of the metal carbonate and/or metal bicarbonate that can react with the acid is a function of the particle size of the metal carbonate and/or metal bicarbonate and the amount thereof present in the two-component system.

Calcium carbonate (CaCO)₃) May be present as one or more calcium carbonate fillers. The one or more calcium carbonate fillers may have a median particle size of about 1 to 50 μm. The calcium carbonate may have a medium to fine particle size. For example, the median particle size of the medium fine calcium carbonate may be about 22 μm. Examples of suitable fine calcium carbonates may be those available from Huber Engineered Materials, Inc. (Atlanta, Ga.)And Q200. The calcium carbonate may have a fine particle size. For example, the fine calcium carbonate may have a median particle size of about 4 μm. Examples of suitable fine calcium carbonates can be those available from Huber Engineered Materials, Inc. (Atlanta, Ga.)Q4. The calcium carbonate may have an ultra-fine particle size. For example, the ultrafine calcium carbonate may have a median particle size of about 1 μm. Examples of suitable ultrafine calcium carbonates may be those available from Huber Engineered Materials, Inc. (Atlanta, Ga.)Q1. The two-component system may comprise medium fine calcium carbonate, ultra fine calcium carbonate, or any combination thereof.

The calcium carbonate may be present in an amount of about 1-25 w% of the a side. The calcium carbonate may be present in an amount of about 4-18 w% of the a side. The calcium carbonate may be present in an amount of about 8-12 w% of the a side. The calcium carbonate may be present in an amount of about 20 w% of the a-side. The calcium carbonate may include about 4-8% by weight fine calcium carbonate on the A-side and about 13-18% by weight medium fine calcium carbonate on the A-side. The calcium carbonate may include about 6% by weight fine calcium carbonate on the a-side and about 15% by weight medium fine calcium carbonate on the a-side. The calcium carbonate may include about 5% by weight fine calcium carbonate on the a-side, and about 5% by weight medium fine calcium carbonate on the a-side. The ratio between medium fine calcium carbonate and fine calcium carbonate may be about 3:1 to 1: 3. The ratio between medium-fine calcium carbonate and fine calcium carbonate may be about 1: 1.

The calcium carbonate may have a skin. The skin may be any material that breaks down during the activation process and/or the swelling process, thereby delaying and/or slowing swelling. The epidermis may be a wax, fatty acid, or combination thereof.

The two-component system may comprise one or more minerals. The one or more minerals (i.e., mineral reinforcement) may structurally enhance the reaction product. The one or more minerals may increase the tensile strength and/or flexural strength of the reaction product. The mineral or minerals may be any suitable silicate mineral including, but not limited to, inosilicates (e.g., wollastonite) and layered silicates (e.g., kaolinite, vermiculite, talc, muscovite, etc.). The characteristic shape of the individual crystals or groups of crystals of the one or more minerals may be needle-shaped. The median particle size of the one or more minerals may be about 10 to 20 μm. The median particle size may be about 12 to 18 μm.

The one or more minerals may include wollastonite (CaSiO)₃). Wollastonite may be relatively pure (i.e., have less than 2 w% of other metal oxide impurities). Wollastonite may contain impurities including one or more oxides of iron, magnesium, manganese, aluminum, potassium, sodium, or strontium (these metals may replace calcium in the mineral structure). Examples of suitable wollastonites may be under the trade name wollastonite12 andwollastonite sold under 8, commercially available from NYCO Minerals, Willsboro, N.Y..

The one or more minerals may be present as part of the a-side and/or B-side. The wollastonite may be present in an amount of about 1 to 10 w% of the A-side and/or the B-side. The wollastonite may be present in an amount of about 3 to 7% by weight on the A-side and/or B-side. Wollastonite may be present in an amount of about 4 w% of the A-side and/or B-side.

The one or more minerals may be modified. For example, the one or more minerals may include kaolinite (i.e., kaolin) that has been calcined (i.e., has been fired at a high temperature for drying). The two-component system may comprise calcined kaolin. Calcined kaolin can facilitate the foaming (e.g., expansion) process. The calcined kaolin can have an average particle size of 1.3 μm as measured by the average stokes equivalent diameter. The calcined kaolin can have an average particle size of 3.2 μm as determined by median Malvern laser measurement. Examples of suitable calcined kaolins can be under the trade name70C Kaolin sold as Kaolin fromLLC (Macon, Georgia, USA).

The calcined kaolin can be present as part of the a-side and/or the B-side. The calcined kaolin can be present in an amount from about 0.25 to 5 w% of the a-side and/or the B-side. The calcined kaolin can be present in an amount from about 1 to 4 w% of the a-side and/or the B-side. The calcined kaolin can be present in an amount of about 2 w% of the a-side and/or the B-side.

The bicomponent system may comprise one or more reinforcing fibers. The reinforcing fibers may structurally reinforce the reaction product. The one or more reinforcing fibers may increase the tensile strength and/or flexural strength of the reaction product. The one or more reinforcing fibers may be present in the a-side and/or the B-side. The one or more reinforcing fibers may be uniformly dispersed in the a-side and/or the B-side. The one or more reinforcing fibers may include polymer fibers and/or glass fibers. The polymer fibers may include nylon, polyamide, polyester, polypropylene, polyethylene, polytetrafluoroethylene, aramid fibers (e.g., nylon, polypropylene, polyethylene, polytetrafluoroethylene, or polypropylene fibers)) Etc., or any combination thereof. The glass fibers may include aluminoborosilicate glass (E glass), soda lime glass (a glass or C glass), electric/chemical resistant glass (E-CR glass), borosilicate glass (D glass), aluminosilicate glass (R glass or S glass), or any combination thereof. The reinforcing fibers may be chopped fibers. The chopped length of the reinforcing fibers may be about 0.1cm or more, 0.3cm or more, and even 0.6cm or more. The chopped length of the reinforcing fibers may be about 2.0cm or less, 1.5cm or less, or even 1.0cm or less. Examples of suitable glass fibers may be chopped strands available from Jushi USA company (colombian).

The reinforcing fibers may be present in an amount of about 0.01 to 3 w% of the a-side and/or B-side. The reinforcing fibers may be present in an amount of about 0.1-1 w% of the a-side and/or B-side. The reinforcing fibers may be present in an amount of about 0.2 w% of the a-side and/or B-side.

The two-component system may comprise hydrophobic silica. Hydrophobic silicas may be used to adjust viscosity (e.g., thickening), control thixotropy, enhance hydrophobicity, or combinations thereof. The hydrophobic silica may be fumed silica. The hydrophobic silica may be surface treated. For example, the hydrophobic silica may be fumed silica surface-treated with polydimethylsiloxane (hereinafter referred to as PDMS) or hexamethyldisilazane (hereinafter referred to as HMDZ). The hydrophobic silica may be present as part of the a-side and/or B-side. Examples of suitable hydrophobic silicas may be provided under the trade nameHydrophobic silica sold by R202 (available from Evonik corporation of Parsippany, N.J.), and also available under the trade designation CAB-O-TS-530 and TS-720 (commercially available from Cabot corporation, Boston, Mass.).

The hydrophobic silica may be present in an amount of about 0.25-6 w% of the A-side and/or B-side. The hydrophobic silica may be present in an amount of about 0.5-4 w% of the A-side and/or B-side. The hydrophobic silica may be present in an amount of about 1-2 w% of the A-side and/or B-side. The hydrophobic silica may be present in an amount of about 0.5-2 w% of the A-side. The hydrophobic silica may be present in an amount of about 3-5 w% of the B-side. The ratio between the hydrophobic silica in the a-side and the B-side may be about 1:6 to 6: 1. The ratio between the hydrophobic silica in the a-side and the B-side may be about 1: 4. The ratio between the hydrophobic silica in the a-side and the B-side may be about 1:2 to 2: 1.

The two-component system may comprise plate alumina. The plate-like alumina may impart to the reaction product high hardness, thermal shock resistance, mechanical shock resistance, high heat capacity, high electrical resistance, or any combination thereof. The plate-like alumina may be present in the a-side and/or the B-side. The plate-like alumina may be alpha-alumina converted to corundum form (i.e., crystalline alumina) and sintered, and may be present as a granular fraction or powder. The tabular alumina may be classified (i.e., separated by size) in the range of about 44 μm to about 4760 μm. The plate alumina may be graded to about 44 μm.

The plate-like alumina may be present in an amount of about 5-20 w% of the a-side and/or B-side. The plate-like alumina may be present in an amount of about 7-18 w% of the a-side and/or B-side. The plate-like alumina may be present in an amount of about 10 w% of the a-side and/or B-side.

The two-component system may comprise one or more functional additives for improving one or more properties of the composition. Examples of suitable functional additives may include antioxidants, antiozonants, ultraviolet absorbers, antistatic agents, colorants, coupling agents, curing agents, flame retardants, blowing agents, heat stabilizers, impact modifiers, lubricants, plasticizers, preservatives, processing aids, stabilizers, and the like, and any combination thereof.

The a-side and/or B-side may have a sufficiently high viscosity at a temperature of about 23 ℃ to prevent accidental discharge of the two-component system to the area adjacent the bead-like dispensing when the two-component system is bead-dispensed onto a workpiece, or to control discharge of the two-component system to the area adjacent the bead-like dispensing when the two-component system is dispensed (i.e., to allow only the desired amount of discharge). The viscosity of the a-side and/or B-side required to avoid accidental flow or control flow may depend on the size of the bead. For example, the thicker the bead distribution of a two-component system, the higher the viscosity required to prevent accidental flow or control flow. The viscosity of the A-side at a temperature of 23 ℃ may be about 20,000-50,000cP, or even 35,000-45,000 cP. The viscosity of the A-side at a temperature of 10 ℃ may be about 280,000-350,000cP, or even 300,000-325,000 cP. The viscosity of the B-side at a temperature of 23 ℃ may be about 20,000-50,000cP, or even 35,000-45,000 cP. The viscosity of the B-side at a temperature of 10 ℃ may be about 130,000-220,000cP, even 175,000-195,000 cP.

After mixing the a-side and the B-side, the two-component system may expand to a volume greater than about 50%, greater than about 100%, greater than about 200%, less than about 800%, less than about 700%, or even less than about 600% of the original volume of the two-component system. The two-component system can expand out of a volume of about 400% to 500% of the original volume of the two-component system. The volume expanded out of the two-component system may be about 400% of the original volume of the two-component system.

The two-component system may be free of curing agents (i.e., typical curing agents) and/or curing accelerators. Typical curing agents include lewis bases (i.e., anionic catalysts), lewis acids (i.e., cationic catalysts), UV catalysts, amines, anhydrides, phenols, thiols, or any combination thereof. In the case of not using the above curing agent, the two-component system can be cured after polymerization reaction occurs between the phosphate ester and the epoxy group and/or the hydroxyl group under the catalysis of phosphoric acid. The two-component system can be expanded and cured by chemical interaction between the phosphate ester and the calcium carbonate. It has been found that the expansion and cure system of the present invention allows for a reduction in the amount of total components (i.e., curing agent, cure accelerator, and blowing agent) and thus a reduction in the complexity of the formulation; however, it will also be more difficult to optimize the required expansion and curing time.

In one non-limiting embodiment of the invention, the two-component system may comprise one or more of the following components in the A-side (first component): liquid epoxy resin, flexible epoxy resin, aliphatic polyfunctional epoxy resin, reactive diluent, aramid fiber, medium-fine calcium carbonate, hydrophobic silicon dioxide and wollastonite. The two-component system may comprise one or more of the following components in the B-side (second component): a first phosphate ester, a second phosphate ester, a third phosphate ester, aramid fibers, and hydrophobic silica.

The two-component system can be mixed in a ratio between the a-side and the B-side of 1:4 to 4: 1. The two-component system can be mixed in a ratio between the a-side and the B-side of 1:2 to 2: 1. The two-component system can be mixed in a ratio between the a-side and the B-side of 1: 1. The two-component system can be mixed in a ratio between the a-side and the B-side of 2: 1.

Two non-limiting example formulations obtained according to the present invention are provided in table 1.

TABLE 1

Table 2 provides technical data at a curing temperature of 23 ℃ for the formulations obtained according to the invention. The "exotherm peak" may refer to the peak temperature reached upon curing and may be a function of the degree of crosslinking and the rate of cure: a higher degree of crosslinking may result in a higher degree of exothermic reaction; a higher cure rate may produce a higher exotherm peak because the reaction product absorbs heat from the exothermic reaction faster than it releases heat. Mechanical properties were determined according to ASTM D1621. The sample was compressed to 50% of the cubic size. The crosshead travel rate was kept constant at 12.7 mm/min.

TABLE 2

Other formulation examples obtained according to the present invention are provided in table 3.

TABLE 3

Table 4 provides technical data at a curing temperature of 23 ℃ for the formulations obtained according to table 3. The compressive modulus may be a function of the compressive stress (force per unit area) applied to the sample and the resulting compression (deformation). Thus, a higher compressive modulus is required. If both samples have a uniform compressive modulus, the lower density sample indicates a stronger matrix for the reaction product, and the reaction product may be a product with a higher degree of crosslinking. When the ratio of density to compressive modulus is observed, if the ratio is low, it may indicate that the matrix of the reaction product is overall strong. The sample designated as "pad" may be a conventional pre-foamed pad. Compression properties were determined according to ASTM D1621 using 25.4mm cubes. The sample was compressed to 50% of the cubic size. The crosshead travel rate was kept constant at 12.7 mm/min.

TABLE 4

The two-component system may be presented as a side-by-side cartridge, drum or drum. The two-component system may be mixed prior to application to the workpiece. The two-component system can be applied to the workpiece by any suitable dispenser and the two-component system is mixed by the dispenser prior to application to the workpiece. For example, as described herein, a two-component system can be dispensed onto a workpiece through a static mixer configured to deliver a curable mixed composition having an appropriate mixing ratio.

The resulting reaction product has excellent adhesion to many substrates and short cure times. The resulting reaction product can have excellent adhesion to glass, metal, polymers (e.g., thermoplastics, thermosets or thermosets, elastomers), or any combination thereof. In particular, the reaction products have excellent adhesion to thermoplastics.

The activatable material may be activated before or after the complete assembly of the profile or profiles to which the two-component system is applied. For example, the activatable material may be dispensed on a first profile and activated, and then a second profile complementary to the first profile may be applied on the first profile. As another example, the activatable material may be dispensed on a first profile and a second profile complementary to the first profile may be dispensed on the first profile, and then the activatable material may be activated. The activatable material that solidifies and/or expands after the profiles are fully assembled may fill the space between the first and second profiles by expanding. The first profile and/or the second profile can have a groove in which the two-component system can be distributed and/or expanded.

The one or more profiles may be draw extruded. The one or more profiles may have any size or shape that can be pultruded. Pultrusion is a method of manufacturing composite structures by impregnating reinforcing fibers with a resin and pulling the reinforcing fibers through a heated stationary mold in which the resin polymerizes. The one or more profiles may have any suitable cross-section. The one or more profiles may have a coherent shape. The one or more profiles may have a shape that varies along a longitudinal axis, a transverse axis, a vertical axis, or a combination thereof. As shown in fig. 1 and 2, the pultruded profile 1 has a large rectangular cross-section portion 3 and a small rectangular cross-section portion 4 connected by a horizontal surface portion 5.

After the one or more profiles are pultruded, an activatable material may be applied to the profiles. The activatable material may be placed in an extruder and then extruded onto the one or more pultruded profiles that have just exited from the pultrusion die. The activatable material may be extruded onto the one or more pultruded profiles in an in-line process to reduce the number of steps required for manufacturing. Pultrusion requires heating while forming the profile or profiles. Once the activatable material is extruded onto the pultruded profile, the residual heat entering the pultruded profile will be sufficient to activate the activatable material. Because the pultruded profile retains some of the heat from the forming process, the time required for the activatable material to expand and cure is reduced. As shown in fig. 1, 2, pultruded profile 1 has activatable material 2 disposed along a large rectangular cross-section 3. The activatable material may be located on any portion of the pultruded profile. The activatable material may substantially cover the profile. The activatable material may be selectively positioned on the profile.

Two-component systems are used in the transportation industry. Two-component systems are used in the automotive field. Two-component systems can be used in applications including, but not limited to, vehicle interiors, vehicle exteriors, HVAC ducts, side mirrors, electronics housings, tail lights, headlamps, and the like.

The present invention provides a method, which may comprise: providing a two-component system comprising an a-side (i.e., a first component) and a B-side (i.e., a second component), wherein the a-side comprises one or more epoxy resins and the B-side comprises one or more phosphate esters and optionally phosphoric acid; the a-side and B-side can be mixed to form a curable composition. The method may include the step of curing the curable composition at a temperature of less than 50 ℃ to form a reaction product. The method may include the step of mixing the first component and the second component to form a reaction product. The method may include the step of curing the product of the reaction between the first component and the second component at a temperature of less than 50 ℃. The method can be used for the a-side containing one or more epoxy resins and/or calcium carbonate. The method can be used for the B side containing one or more phosphate esters and/or phosphoric acid. The method can be used on the a-side and/or the B-side containing one or more additives.

Gaskets exhibiting sufficient flame retardancy may be obtained in accordance with the description herein to meet one or more requirements to demonstrate flame retardancy (e.g., to meet the vertical burn and/or smoke density requirements (or some other requirement) specified in U.S. interior of the vehicle regulations, including but not limited to 14 c.f.r. § 25.853(a), and the cited appendix F and procedures cited therein), all of which are incorporated herein by reference for all purposes.

As used herein, the present invention contemplates that any item in the classification (list) may not be listed in the classification and/or any item in the Markush group may not be listed in the group unless otherwise indicated.

Any numerical range recited herein includes all values from the lower value to the upper value, in increments of one unit, provided that there is an interval of at least two units between any lower value and any upper value, unless otherwise stated. For example, if a component level, property, or process variable (e.g., temperature, pressure, time, etc.) is specified to have a value of, for example, 1 to 90, preferably 20 to 80, and more preferably 30 to 70, then intermediate values (e.g., 15 to 85, 22 to 68, 43 to 51, 30 to 32, etc.) are also considered to be within the teachings of this specification. Likewise, various intermediate values are also within the scope of the present invention. For values less than 1, 0.0001, 0.001, 0.01, or 0.1 can be considered as a unit as desired. These are merely illustrative of specific intent and all possible combinations of numerical values between the lower and upper limit values should be considered expressly stated in this application in a similar manner. It can be seen that the amounts expressed herein as "parts by weight" also encompass the same range in weight percent. Thus, a recitation of a range in terms of "at least x parts by weight of the resulting composition" also encompasses the same range in terms of weight percent of the resulting composition.

All ranges are inclusive of the endpoints and all numbers between the endpoints unless otherwise stated. The word "about" or "approximately" in relation to a range is appropriate to describe both ends of the range. Thus, "about 20-30" is intended to encompass "about 20 to about 30" and at least the endpoints specified. The combination of the word "about" or "approximately" and numerical values is intended to encompass the recited amount as well as approximations of the recited amount unless otherwise indicated. For example, a statement of "about 100" is intended to encompass 100.

The disclosures of all articles and references, including patent applications and publications, are incorporated herein by reference for all purposes. The phrase "consisting essentially of … …" is used to describe a combination that includes the identified elements, components, or steps, as well as other elements, components, or steps that do not materially affect the basic and novel characteristics of the combination. The words "comprises" or "comprising" are used herein to describe combinations of elements, components, or steps, and also to encompass embodiments that consist of, or consist essentially of, such elements, components, or steps.

A plurality of elements, components, or steps may be provided by a single integrated element, component, or step. Alternatively, a single integrated element, ingredient, component or step may be divided into multiple separate elements, ingredients, components or steps. The use of "a" or "an" to describe an element, ingredient, component or step is not intended to exclude further elements, ingredients, components or steps.

It is to be understood that the above description is intended to be illustrative, and not restrictive. Many other embodiments and many applications besides the examples provided will be apparent to those of skill in the art upon reading the above description. The scope of the invention should, therefore, be determined not with reference to the above description, but instead should be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled. The disclosures of all articles and references, including patent applications and publications, are incorporated herein by reference for all purposes. The omission in the following claims of any aspect of subject matter disclosed herein is not to be construed as a disclaimer of such subject matter, nor is it to be construed by the inventors that such subject matter is considered part of the disclosed subject matter.