Epoxy Composites

Abstract

A flame-retardant epoxy resin composition for preparing a flame-retardant fiber composite material: (a) at least one epoxy resin, (b) at least one flame retardant for improving the combustion performance of a carbon fiber reinforced epoxy composite material, (c) at least one mold release agent, (d) at least one curing agent, and (e) at least one catalyst; a prepreg prepared using the above epoxy resin composition; and a flame-retardant fiber composite material prepared using the above prepreg.

Description

[Technical field]

[0001] The present invention relates to an epoxy resin composition, more specifically, the present invention relates to a flame retardant epoxy resin composition for preparing a fiber composite material. [Background technology]

[0002] Epoxy carbon fiber composites are increasingly being used in the automotive, aerospace, electronics, and other industries due to the considerable strength and stiffness that carbon fiber composites offer, and the potential for significant weight savings when using such carbon fiber composites. Although epoxy carbon fiber composites offer advantages in terms of weight savings compared to metals or metal alloys, epoxy carbon fiber composites are inferior in terms of the ability of epoxy carbon fiber composites to retard the spread of fire. This limits epoxy carbon fiber composites for use in applications that must meet very stringent flame retardant requirements. Materials used in applications such as electrical / electronic equipment, or in certain segments within the transportation market such as powerboat racing, aerospace, defense, rail, and hazardous materials vehicles, are often highly required to be flame retardant to prevent accidents such as the ignition or burning of equipment casings or parts, which may occur if the casings or parts are exposed to heat generated inside the equipment or high temperatures outside the equipment.

[0003] Epoxy carbon fiber composites are usually based on thermosetting resins such as diglycidyl ether of bisphenol A (DGEBA). Such thermosetting resins are not self-extinguishing and exhibit strong burning and dripping when exposed to flame. The flame retardancy of epoxy carbon fiber composites can be improved by adding flame retardant (FR) agents. Traditionally, halogenated flame retardants have been most widely used. Although halogenated FR agents are very effective when used in composites, they may generate harmful gases such as hydrogen halides or organic halogen compounds during the period between when the composite ignites and when the fire is extinguished. It is also known that polyhalogenated dioxins are released when plastic materials containing halogenated flame retardants are incinerated at insufficiently high temperatures (<900 degrees Celsius). Much effort has been made over the past decade or so to develop non-halogenated FR agents. Known non-halogen FR agents generally improve the flame retardancy of epoxy-argon fiber composites containing such non-halogen FR agents, but in many cases, the incorporation of non-halogen FR agents into epoxy formulations may be accompanied by a reduction in the thermal and mechanical properties of composites made from such epoxy formulations. The addition of FR agents to resin formulations also tends to significantly increase the viscosity of the matrix resin (e.g., >10 Pascal seconds (Pa.s) at 110°C). Impregnating carbon fiber fabrics with high viscosity matrix resins is difficult to achieve. Epoxy carbon fiber composites for automotive applications require the use of low viscosities (e.g., <10 Pa.s) at injection temperatures (e.g., about 100°C to 130°C) for good fiber impregnation and high cure glass transition temperatures (Tg). Additionally, epoxy carbon fiber composite parts intended for use in high-speed automated manufacturing systems also require fast cure speeds and negligible prepreg tack for automated processing.

[0004] There are known epoxy composites that have the required cure speed and physical or mechanical properties, but none of the known epoxy composites combine the required cure speed, physical properties, and mechanical properties with flame retardant properties. For example, WO2017 / 066056 discloses an epoxy resin composition containing an epoxy resin component (A) that includes an oxazolidone, an epoxy resin component (B), dicyandiamide (dicyandiamide) particles, and an epoxy-soluble latent catalyst. The dicyandiamide particles have a particle distribution in which 98 percent (%) of the dicyandiamide particles have a diameter less than 10 microns (μm) and at least 35% of the dicyandiamide particles have a particle size greater than 2 μm. The epoxy resin composition disclosed in WO2017 / 066056 does not include a flame retardant.

[0005] Other epoxy formulations containing flame retardants are known in the art, but such known epoxy formulations do not have the required Tg and / or tack-free properties desired for automated processing. For example, EP1359174A1, US2014 / 0010979A1, EP2439222A1, and EP2543693B1 describe various epoxy resin compositions containing flame retardants, but the above references do not provide epoxy resin compositions with the desired Tg and / or tack-free properties.

[0006] Still other epoxy formulations containing flame retardants are known in the art, but such known epoxy formulations may provide epoxy resin compositions that do not achieve one or more properties, such as sufficient flame retardancy, Tg and / or tack-free properties, because they use different combinations of components to constitute the compositions. For example, KR1530754B1, JP2011 / 148938A, and KR2017 / 022874A describe epoxy resin compositions that use different combinations of epoxy resins, FR agents, curing agents, and / or catalysts. Summary of the Invention [Problem to be solved by the invention]

[0007] The present invention relates to an oxazolidone-based epoxy resin formulation or composition comprising a selected and dosage amount of a non-halogenated phosphorus-containing (phosphinate) flame retardant, which is added to the oxazolidone-based epoxy resin composition to improve the flammability performance of carbon fiber reinforced epoxy composites made from such flame retardant oxazolidone-based epoxy resin composition.

[0008] In one embodiment, the present invention comprises a flame retardant epoxy resin composition for preparing a flame retardant fiber composite material, comprising: (a) at least one oxazolidone-based epoxy resin; (b) at least one non-halogenated phosphorus-containing flame retardant for improving the fire performance of a carbon fiber reinforced epoxy composite material made from the flame retardant epoxy resin composition; (c) at least one mold release agent; (d) at least one curing agent; and (e) at least one catalyst.

[0009] In another embodiment, the present invention comprises a flame retardant fiber composite prepared with the above epoxy resin composition.

[0010] The present invention provides epoxy resin compositions with the required cure speed, physical or mechanical properties, and flame retardancy by using a unique preselected combination of solid and liquid epoxy resins and phosphorus-based FR agents. Advantages of the present compositions include the use of FR agents with average particle size less than 5 μm to avoid particulate filtration by the carbon fiber reinforcement. The epoxy carbon fiber prepregs of the present invention are tack-free at room temperature (e.g., about 22° C.) and cure at 150° C. in less than 3 minutes (min). The carbon fiber composites have a cure Tg greater than 150° C., and the cured composites can achieve a UL94 V-0 classification. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0011] "Fire resistant agent" and "flame retardant" (abbreviated herein as "FR") are terms that may be used interchangeably herein and refer to materials, substances, or additives used to prevent or slow the spread of fire or to reduce the intensity of a fire. Materials, such as the carbon fiber woven materials described herein, treated with the curable FR epoxy resin compositions described herein are "slow-burning" or "self-extinguishing", such that the materials do not melt or drip when exposed to heat or an open flame (i.e., an ignition source). Flame retardants are not "non-flammable" or "flame-retardant" agents, but instead, flame retardants herein are materials designed to slow the spread of fire. When exposed to an ignition source, the flame retardant is activated by the presence of the ignition source and functions to suppress the fire, i.e., the flame retardant is intended to prevent or slow the further development of ignition or combustion. Thus, fire resistant materials inhibit the spread of fire, i.e., the fire retardant acts to prevent or reduce the probability of the spread of fire.

[0012] In one general embodiment, a flame-retardant (FR) composite of the invention includes a FR epoxy resin formulation or composition, and a carbon fiber reinforcement impregnated with the FR epoxy resin composition cured to form a FR carbon fiber composite.

[0013] In a broad embodiment, a curable FR epoxy resin composition useful in the present invention comprises: (a) at least one epoxy resin (i.e., at least one oxazolidone group-containing solid epoxy resin), such as, for example, a solid epoxy resin that can be an oxazolidone-based solid epoxy resin; (b) at least one non-halogenated phosphorus-containing flame retardant for improving the fire performance of a fiber-reinforced epoxy composite, such as at least one non-halogenated phosphorus-containing flame retardant that provides a fiber-reinforced epoxy resin composite that exhibits flame retardancy of at least UL94 V-1 standard while retaining mechanical properties such as tensile strength and stiffness; (c) at least one mold release agent; (d) at least one curing agent; and (e) at least one catalyst.

[0014] The curable FR epoxy resin composition of the invention can include at least one epoxy resin (i.e., the epoxy component can be a single epoxy resin or a mixture / combination of two or more epoxy resins). In another embodiment, the curable FR epoxy resin composition of the invention can contain a mixture or combination of (1) at least one epoxy resin as a first resin and (2) a second resin different from the epoxy resin. When two or more different resins are present, the epoxy resin(s) is generally the major component of the curable resin composition.

[0015] A wide range of epoxy resins may be suitable for use as the epoxy resin component of the curable composition. The epoxy resins useful for preparing the curable composition may include, for example, liquid epoxy resins, epoxy novolac resins, solid epoxy resins, or any combination thereof. The epoxy resins useful in the present invention may be any known aliphatic, cycloaliphatic, or aromatic epoxy resins. In one preferred embodiment, epoxy resins with aromatic groups and epoxy resins containing either glycidyl amine structures and glycidyl ether structures may be used. In another embodiment, cycloaliphatic epoxy resins may also be preferably used.

[0016] Illustrative epoxy resins useful in the present invention containing a glycidyl amine structure include the various isomers of tetraglycidyldiaminodiphenylmethane, N,N,O-triglycidyl-p-aminophenol, N,N,O-triglycyl-m-aminophenol, N,N,O-triglycyl-3-methyl-4-aminophenol, triglycylaminocresol, and mixtures thereof.

[0017] The epoxy resin containing a glycidyl ether structure can include, for example, bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol S type epoxy resin, phenol novolac type epoxy resin, cresol novolac type epoxy resin, and mixtures thereof.

[0018] The epoxy resins useful in the present invention may have, for example, non-reactive substituents in the aromatic ring structure. For example, the non-reactive substituents may include alkyl groups (e.g., methyl, ethyl, or isopropyl), aromatic groups (e.g., phenyl), alkoxyl groups, aralkyl groups, halogen groups (e.g., chlorine or bromine), and mixtures thereof.

[0019] In one preferred embodiment, the epoxy resin or mixture thereof may itself be a non-tacky solid at 23° C. In another preferred embodiment, the epoxy resin or mixture thereof may itself be heat softened at a temperature of 40° C. to 80° C., and in another embodiment, 40° C. to 65° C. In yet another embodiment, the epoxy resin may include at least one epoxy resin that is solid at 23° C., and in yet another embodiment, the epoxy resin composition may contain a mixture of one or more epoxy resins that are solid at 23° C. and one or more epoxy resins that are liquid at 23° C.

[0020] The epoxy resin or mixture thereof may have, for example, an epoxy equivalent weight (EEW) of at least 210 grams / equivalent (g / eq), or at least 220 g / eq, and in one embodiment up to 1,000 g / eq, in another embodiment up to 500 g / eq, in yet another embodiment up to 350 g / eq, or in yet another embodiment up to 300 g / eq.

[0021] The epoxy resin or mixture thereof may have a number average epoxy functionality of, for example, in one embodiment, at least 2.4 epoxy groups per molecule, in another embodiment, at least 2.5 epoxy groups per molecule, or in yet another embodiment, at least 2.6 epoxy groups per molecule. Further, the number average epoxy functionality may be, for example, up to 6 epoxy groups per molecule in one embodiment, up to 4 epoxy groups per molecule in another embodiment, up to 3.5 epoxy groups per molecule in yet another embodiment, or up to 3.0 epoxy groups per molecule in yet another embodiment.

[0022] In some preferred embodiments of the present invention, the epoxy resin may contain at least one polyglycidyl ether of a polyphenol. The polyglycidyl ether of a polyphenol may include, for example, (i) diglycidyl ethers of polyhydric phenolic compounds such as resorcinol, catechol, hydroquinone, biphenol, bisphenol A, bisphenol AP (1,1-bis(4-hydroxyphenyl)-1-phenylethane), bisphenol F, bisphenol K, bisphenol M, and tetramethylbiphenol, (ii) diglycidyl ethers of aliphatic glycols and polysulfides such as diglycidyl ethers of C2-24 alkylene glycols and poly(ethylene oxide) or poly(propylene oxide) glycols. (iii) polyglycidyl ethers of alkyl-substituted phenol-formaldehyde resins, such as phenol-formaldehyde novolac resins (epoxy novolac resins), epoxy cresol novolac resins, phenol-hydroxybenzaldehyde resins, and cresol-hydroxybenzaldehyde resins, each having three or more epoxy groups per molecule; (iv) oxazolidone group-containing polyglycidyl ethers of phenolic compounds, such as those described in U.S. Patent No. 5,112,932. Such epoxy resins include reaction products of diisocyanates, such as diphenylmethane diisocyanate or toluene diisocyanate, with diglycidyl ethers of diphenols, such as resorcinol, catechol, hydroquinone, biphenol, bisphenol A, bisphenol AP (1,1-bis(4-hydroxyphenyl)1-phenylethane), bisphenol F, bisphenol K, and tetramethylbiphenol.These epoxy resins may have, for example, an epoxy functionality of 1.9 to 2.5 in one embodiment, and 1.9 to 2.2 in another embodiment, and an epoxy equivalent weight of, for example, 300 to 500 in one embodiment, and 325 to 450 in another embodiment; (v) dicyclopentadiene-phenolic resins and dicyclopentadiene substituted phenolic resins; (vi) partially higher epoxy resins of any of types (i), (ii), or (iii) above; and (vii) any combination of two or more of the above epoxy resins.

[0023] Many of the above epoxy resins of types (i)-(vi) are commercially available. And some of the commercially available epoxy resin products may often be blends of two or more of the above epoxy resins. For example, commercially available polyglycidyl ethers of bisphenol A and bisphenol F that may be useful in the present invention include those sold by Olin Corporation under the names DER® 330, DER 331, DER 332, DER 354, DER 383, DER 661, and DER 662 resins. Generally, such epoxy resins have more than two epoxy functional groups. Commercially available diglycidyl ethers of polyglycols may include DER 732 and DER 736 available from Olin Corporation.

[0024] In other embodiments, commercially available epoxy novolac resins that may be useful in the present invention may include, for example, DEN® 354, DEN 431, DEN 438, and DEN 439 available from Olin Corporation. Generally, these epoxy novolac resin products may have, for example, an epoxy equivalent weight of 150 to 200 in one embodiment, and may have, for example, an epoxy functionality of 2.2 to 5.0 in one embodiment, and 2.6 to 4.0 in another embodiment. Another suitable commercially available epoxy resin containing oxazolidone groups and that may be useful in the present invention may include DER 6508 (available from Olin Corporation).

[0025] Other embodiments that may be useful in the present invention may include commercially available epoxy cresol novolac resins such as Huntsman Araldite ECN1273, Epon® 164 and Epon® 165 from Hexion, and Epiclon® N-660, Epiclon N-664, Epiclon N-670, Epiclon N-673, Epiclon N-680, Epiclon N-690, and Epiclon N-695 from DIC Americas. Generally, these epoxy cresol novolac resin products may have, for example, an epoxy equivalent weight of 180 to 250 in one embodiment, and may have an epoxy functionality of, for example, 2.2 to 5.0 in one embodiment, and 2.6 to 4.8 in another embodiment.

[0026] In one embodiment of the present invention, the epoxy resin useful in the epoxy resin composition of the present invention may include a liquid epoxy resin in combination with an epoxy novolac resin. For example, the epoxy resin composition may contain a liquid epoxy resin that is a diglycidyl ether of bisphenol A and an epoxy novolac resin that is a polyglycidyl ether of phenol-formaldehyde novolac. In one embodiment, based on the total weight of all epoxy resins in the epoxy resin composition, the diglycidyl ether of bisphenol A epoxy resin may be present in the composition in an amount of 0 weight percent (wt%) to 65 wt%, and the epoxy novolac resin may be present in the composition in an amount of 0 wt% to 70 wt%. In one preferred embodiment, based on the total weight of all epoxy resins in the epoxy resin composition, the diglycidyl ether resin may be present in the composition in an amount of 10 wt% to 40 wt%, and the epoxy novolac resin may be present in the composition in an amount of 15 wt% to 62 wt%. In another preferred embodiment, the diglycidyl ether liquid epoxy resin may be present in the composition in an amount from 15% to 30% by weight, and the epoxy novolac resin may be present in the composition in an amount from 25% to 46% by weight, based on the total weight of all epoxy resins in the epoxy resin composition.

[0027] In another embodiment, when the epoxy component in the composition is only a liquid epoxy resin, the amount of liquid epoxy resin present in the epoxy resin composition, based on the total weight of the components in the epoxy resin composition, may range from 35% to 90% by weight in one embodiment, from 45% to 85% by weight in another embodiment, and from 55% to 75% by weight in yet another embodiment.

[0028] In yet another embodiment, when the epoxy component in the composition is only a solid epoxy resin, the amount of solid epoxy resin useful in the epoxy composite composition can range from 10% to 65% by weight, from 15% to 55% by weight in another embodiment, and from 20% to 45% by weight in still another embodiment, based on the total weight of all epoxy resins in the epoxy resin composition. In one preferred embodiment, the amount of solid epoxy resin in the epoxy resin composition can range from 25% to 43% by weight, based on the total weight of the components in the epoxy resin composition.

[0029] In yet another embodiment, when the epoxy component in the curable resin composition contains a mixture of any of the above types of epoxy resins (a)-(f), such epoxy resins together represent at least 50 wt.%, at least 75 wt.%, at least 90 wt.%, or at least Alternatively, the combination of epoxy resins used in the composition may comprise 100% of the total weight of all epoxy resins.

[0030] In still yet another embodiment, the curable resin composition may include a combination of (1) at least one diglycidyl ether of a bisphenol product, (2) at least one epoxy novolac resin product, and (3) at least one oxazolidone-containing epoxy resin product, these three products together comprising 90% to 100% or 95% to 100% by weight of the total weight of all epoxy resins present in the curable resin composition.

[0031] In some embodiments, other epoxy resins may be present in the composition, but in such embodiments, the other epoxy resins are present in small amounts, if at all. Among these other epoxy resins are cycloaliphatic epoxides, including those described in U.S. Pat. No. 3,686,359. These cycloaliphatic epoxides may include, for example, (3,4-epoxycyclohexyl-methyl)-3,4-epoxy-cyclohexane carboxylate, bis-(3,4-epoxycyclohexyl) adipate, vinylcyclohexene monoxide, and mixtures thereof.

[0032] In other embodiments, the epoxy resins that may be used in the compositions are not necessarily rubber-modified and do not necessarily contain polyether groups, although rubber modification and modification with toughening agents containing epoxy-terminated polyethers and / or polyethers with capped terminal isocyanate groups are within the scope of the present invention.

[0033] The FR agent that can be used to prepare the FR epoxy resin composition of the present invention can include one or more flame retardants known in the art. The FR agent can include a phosphorus-containing material, and can be either a chemical element itself, such as red phosphorus, or alternatively, a variety of inorganic or organic compounds containing phosphorus. For example, the FR agent can be selected from the group consisting of elemental red phosphorus, melamine phosphate, dimelamine phosphate, melamine pyrophosphate, triaryl phosphate, resorcinol bis(diphenyl phosphate), tris(chloropropyl) phosphate, ammonium polyphosphate, phosphinic acid derivatives, inorganic phosphinates, such as aluminum phosphinate, or metal salts of organic phosphinic acids and mixtures thereof, and the like. Aluminum diethylphosphinate can be used in one preferred embodiment.

[0034] When using a solid FR agent, it should preferably have a particle size of less than 5 μm. Generally, when the epoxy resin composition contains solid particles with a size of more than 5 μm, the particles tend to be filtered by the carbon fiber fabric during the infusion process. Filtering the FR agent may have a negative effect on the flame retardancy of the composite article.

[0035] The amount of FR agent used to make the FR epoxy resin composition can be, for example, 1 wt% to 30 wt% in one embodiment, 5 wt% to 25 wt% in another embodiment, and 10 wt% to 20 wt% in yet another embodiment. Adding more than 30 wt% of FR agent can reduce the thermal and mechanical properties of the molded composite article. When using solid FR agents, adding more than 30 wt% of FR agent to the formulation can significantly increase the viscosity (e.g., greater than 10 Pa.s at the injection temperature) and therefore reduce the processability of the resin.

[0036] The mold release agent that can be used to prepare the FR epoxy resin composition of the present invention can include one or more mold release agents known in the art. For example, the mold release agent in the curable FR epoxy resin composition can include at least one internal mold release agent (IMR) as component (c). An IMR agent is a substance contained within the curable resin composition that reduces adhesion of the cured composition to a mold or other surface to which the curable resin composition has been cured. Examples of IMR agents include fatty acids having in one embodiment 16 or more carbon atoms, and in another embodiment having 18 carbon atoms to 36 carbon atoms. Also useful in the present invention can be IMR agents such as alkali metal or ammonium salts, monoalkyl esters, monoalkyl amides, and diglycerides and / or triglycerides of such fatty acids, and mixtures thereof. Useful types of internal mold release agents include mixtures of fatty acids having 18 carbon atoms to 36 carbon atoms and diglycerides and / or triglycerides of fatty acids having 10 carbon atoms to 36 carbon atoms. In one preferred embodiment, the IMR agent may include a montanic acid ester of triglycerol, such as Licolub WE4, available from Clariant.

[0037] The IMR agent can be present in the curable FR epoxy resin composition in an amount effective to reduce adhesion of the cured composition to a mold or other surface. A suitable amount of IMR agent present in the curable composition can be, for example, at least 0.5 parts by weight per 100 parts by weight of epoxy resin(s) (PHR) in one embodiment, at least 1 PHR in another embodiment, at least 1.5 PHR to up to 10 PHR in yet another embodiment, up to 7 PHR in yet another embodiment, up to 5 PHR in yet another embodiment, or up to 4 PHR in yet another embodiment.

[0038] The curing agent that can be used to prepare the FR epoxy resin composition of the present invention may include one or more curing agents known in the art that are used to cure epoxy resins. In one preferred embodiment, the curing agent useful in the curable epoxy resin composition includes at least one latent curing agent. A latent curing agent should have an activation temperature of at least 100° C. in one embodiment, and at least 120° C. in another embodiment. The curing agent is latent because it cures (crosslinks) the epoxy resin when heated to a temperature of at least 100° C. or higher, but does not cure the resin (or cures very slowly) at room temperature or even at temperatures up to at least 50° C. The curing agent may be latent because it has a high melting temperature (e.g., above 200° C.) due to, for example, blocked reactive groups, encapsulation, and / or has limited solubility in the epoxy resin (or mixture) until exposed to high temperatures (e.g., below 150° C.).

[0039] The activation temperature of a hardener can be evaluated by combining the hardener with a diglycidyl ether of bisphenol A having an epoxy equivalent weight of 182 to 192 in a stoichiometric ratio, applying the combination between two substrates, heating at various temperatures for 2 hours, and then measuring in each case the lap shear strength according to DIN ISO 1465. Another sample can be cured for 30 minutes at 180 °C, this condition representing the "fully cured" condition. The "activation temperature" refers to the minimum curing temperature at which the combination achieves a lap shear strength of at least 30% of that obtained under "fully cured" conditions.

[0040] Suitable latent hardeners useful in the compositions of the present invention may include, for example, boron trichloride / amine and boron trifluoride / amine complexes; melamine; diallyl melamine; aminotriazoles such as 3-amino-1,2,4-triazole; dicyandiamide; guanamines such as methylguanidine, dimethylguanidine, trimethylguanidine, tetramethylguanidine, methylisobiguanidine, dimethylisobiguanidine, tetramethylisobiguanidine, heptamethylisobiguanidine, hexamethylisobiguanidine, acetoguanamine, and benzoguanamine, and mixtures thereof. Other examples of suitable latent hardeners that may be used in embodiments of the present invention may include hydrazides such as adipic acid dihydrazide, stearic acid dihydrazide, isophthalic acid dihydrazide, and terephthalic acid dihydrazide; semicarbazides; cyanoacetamide; aromatic polyamines such as diaminodiphenyl sulfone; and mixtures thereof. In one embodiment, for example, a mixture of guanamine and dihydrazide can be used. In one preferred embodiment, the use of dicyan, isophthalic dihydrazide, adipic dihydrazide and 4,4'-diamino-diphenylsulfone can be used. In yet another preferred embodiment, the hardener can be dicyan. A suitable dicyan latent hardener that can be used in the embodiments of the present invention is available from AC Catalysts Inc. under the product name Technicure Nanodicy.

[0041] In a preferred embodiment, the hardener is a finely divided latent hardener such as dimethicone. Typically, the finely divided latent hardener has a particle distribution in which 98% of the particles have a maximum particle diameter less than 10 microns (μ) and at least 35% of the particles have a particle diameter less than 2μ, providing a faster cure rate for the epoxy resin composition. Fast cure rates are particularly desirable in automated applications where high throughput is required for the production of molded articles and molded parts.

[0042] In one preferred embodiment, the latent curing agent has a particle size distribution in which 98% of the particles have a maximum particle diameter less than 6μ, and in another embodiment, 98% of the particles have a maximum particle diameter less than 4μ. In yet another embodiment, at least 45% of the particles have a diameter less than 2μ, in yet another embodiment, at least 55% of the particles have a diameter less than 2μ, and in yet another embodiment, at least 90% of the particles have a diameter less than 2μ. In a preferred embodiment, 100% of the particles have a diameter less than 2μ. Particle size can be measured with a laser diffraction system, such as a Beckman Coulter LS13-320 laser diffraction particle size analyzer equipped with a Tornado dry powder system.

[0043] The latent curing agent in the epoxy resin composition is present in an amount sufficient to cure the epoxy resin. In one general embodiment, the latent curing agent may be present in the composition in an amount sufficient to provide at least 0.75 epoxy reactive groups per epoxide group provided by the epoxy resin (or mixture thereof). The amount may be at least 0.85 epoxy reactive groups per epoxide group in another embodiment, at least 0.90 epoxy reactive groups per epoxide group in yet another embodiment, or at least 0.95 epoxy reactive groups per epoxide group in yet another embodiment. In other embodiments, the curing agent may provide up to 1.5 epoxy reactive groups per epoxy group, up to 1.25 epoxy reactive groups per epoxy group, up to 1.15 epoxy reactive groups per epoxy group, up to 1.10 epoxy reactive groups per epoxy group, up to 1.05 epoxy reactive groups per epoxy group, or up to 1.02 epoxy reactive groups per epoxy group.

[0044] The amount of curing agent contained in the epoxy resin composition is present in an amount relative to the total amount of epoxy resin in the composition. The amount of curing agent present in the epoxy resin composition is an amount appropriate for curing all epoxy resins used in the epoxy resin composition, and is appropriately controlled according to the type of epoxy resin used and the curing agent used. For example, the amount of curing agent used to make the FR epoxy resin composition can be, for example, 5% to 15% by weight in one embodiment, 6% to 12% by weight in another embodiment, and 7% to 8% by weight in yet another embodiment, based on the total weight of the epoxy resin composition.

[0045] The curable FR epoxy resin composition of the present invention may include one or more accelerators for the reaction of the epoxy resin in the presence of a curing agent (such as diacetate). The accelerator or curing catalyst may be selected from catalysts known in the art. The resin composition includes at least one accelerator (or curing catalyst) that may also be encapsulated (or blocked) or otherwise includes a latent type accelerator that is only activated when exposed to high temperatures (e.g., above 100°C). The latency of the catalyst may be directly attributable to the chemical structure of the catalyst. For example, the actual catalytically active species of a blocked latent catalyst generally does not exist until it is generated by an unblocking reaction that typically occurs at the aforementioned high temperatures used during the molding process. The accelerator additive or latent catalyst may also be soluble in the epoxy resin of the curable composite composition, so that when solubilized, the solubilized catalyst may be latent until it is heated to the aforementioned high temperatures.

[0046] As used herein, the term "soluble" with respect to a latent catalyst requires that the catalyst is substantially dissolved in the epoxy resin composition prior to injecting the epoxy resin composition into a structural material such as a fibrous material as described herein below. "Substantially dissolved" in one embodiment herein means that greater than 90% of the catalyst is dissolved in the epoxy resin composition, in another embodiment greater than 95% of the catalyst is dissolved in the epoxy resin composition, and in yet another embodiment 100% of the catalyst is dissolved in the epoxy resin composition. Typically, it is desirable to dissolve the catalyst in the epoxy resin composition during mixing of the epoxy resin composition.

[0047] Examples of accelerators that may be used in embodiments of the present invention include urea, substituted ureas, modified imidazoles, and mixtures thereof. For example, ureas useful in the compositions of the present invention include toluene bis-dimethyl urea, Various aliphatic urea compounds, such as p-chlorophenyl-N,N-dimethylurea, 3-phenyl-1,1-dimethylurea, 3,4-dichlorophenyl-N,N-dimethylurea, N-(3-chloro-4-methylphenyl)-N',N'-dimethylurea, the urea compounds described in EP 1 916 272, and mixtures thereof may be included. Other suitable latent catalysts useful in the present invention include, for example, tert-acrylic or alkylene amines such as benzyldimethylamine; 2,4,6-tris(dimethylaminomethyl)-phenol; piperidine or a derivative thereof; 2,4-diamino-6-[2'-methylimidazolyl-(1')]-ethyl-s-triazine, 2,4-diamino-6-[2'-methylimidazolyl-(1')]-ethyl-s-triazine isocyanuric acid adduct dehydrate; C1-C 12Alkylene imidazoles or N-arylimidazoles such as 2-phenyl-imidazole, 2-methylimidazole, 1-methylimidazole, 2-ethyl-4-methylimidazole, 4,4'-methylene-bis(2-ethyl-5-methylimidazole) 2-ethyl-2-methylimidazole, or N-butylimidazole and 6-caprolactam; 2,4,6-tris(dimethylaminomethyl)phenol incorporated in a poly(p-vinylphenol) matrix (as described in EP 0197892) or 2,4,6-tris(dimethylaminomethyl)phenol incorporated in a novolac resin, including those described in U.S. Pat. No. 4,701,378; and mixtures thereof.

[0048] In one preferred embodiment, the soluble latent catalyst useful in the present invention can be the above-mentioned blocked urea catalyst, which is latent and soluble in epoxy resin.An example of a suitable latent urea catalyst that can be used in the embodiment of the epoxy resin composite composition of the present invention can be toluene bis-dimethylurea ("TBDMU").

[0049] The curing catalyst used to make the FR epoxy resin composition should be present in the epoxy resin composition in a catalytically effective amount. For example, such a suitable catalytically effective amount may be from 0.1 PHR to 10 PHR in one general embodiment, from 0.25 PHR to 5 PHR in another embodiment, and from 1 PHR to 5 PHR in yet another embodiment.

[0050] The curable epoxy resin composition may contain various other optional ingredients, compounds, or additives as component (f). Optional additives that may be added to the curable resin formulation of the present invention may include, for example, one or more reaction inhibitors, diluents, toughening agents, rubbers, plasticizers, extenders, colorants, smoke suppressants, thixotropic agents, adhesion promoters, biocides, antioxidants, other cocatalysts, other accelerators, other flame retardants or fire resistant agents, surfactants, flow modifiers, stabilizers, and mixtures thereof. The curable resin composition may also contain finely divided solids such as calcium carbonate, fumed silica, and / or carbon nanotubes that fill the gaps between fibers at or near the surface of the molding compound and the cured composite to provide a smoother surface. A typical epoxy resin composition may also contain some fillers or other functional chemicals for any intended application.

[0051] The amount of the optional components when used in the curable FR epoxy resin composition can be from 0 wt % to 10 wt % in one embodiment, from 0.01 wt % to 5 wt % in another embodiment, and from 0.1 wt % to 5 wt % in yet another embodiment, based on the total weight of the epoxy resin composition.

[0052] In general, the process for making the FR epoxy resin composition includes mixing (a) at least one epoxy resin, (b) at least one non-halogenated phosphorus-containing flame retardant for improving the fire performance of fiber-reinforced epoxy composites, (c) at least one mold release agent, (d) at least one curing agent, and (e) at least one catalyst.

[0053] In one embodiment, and as one non-limiting example of the present invention, a curable FR epoxy resin composite composition can be prepared by mixing 80% to 90% by weight of an epoxy resin, 1% to 20% by weight of a non-halogenated phosphorus-containing flame retardant, 6% to 8% by weight of a curing agent, 2% to 5% by weight of an accelerator, and 2% to 5% by weight of an IMR agent, based on the weight of all components in the composition. Additional optional compounds can also be included in the curable FR epoxy resin composite composition. Once the FR epoxy resin composition is formed, the composition can be combined with a structural material, such as a woven mat of carbon fiber or glass fiber, to produce a composite article.

[0054] As an illustration of the FR epoxy composition of the present invention, and not limited thereby, the FR epoxy resin composition can be prepared, for example, by mixing the following: (a) 30.23 wt% of a first epoxy resin (e.g., DEN438 available from Olin), (b) 28.76 wt% of a second epoxy resin (e.g., DER6508 available from Olin), (c) 16.19 wt% of a third epoxy resin (e.g., DER331 available from Olin), (d) 1.88 wt% of a release agent (e.g., Licolub WE-4 available from Clariant), (e) 6.89 wt% of a first hardener (e.g., Technicure Nanodicy available from AlzChem), (f) 3.01 wt% of TBDMU (e.g., Omicure U410 available from CVC Thermoset Specialties), and (g) 13.04 wt% of a FR agent (e.g., Exolit OP 945 available from Clariant).

[0055] The above components of the FR epoxy composite composition may be mixed together in conventional mixing equipment under conventional mixing conditions known in the art. One or more additional optional compounds may be added to the resin formulation before or during mixing, as needed. In general, mixing of the above components that make up the curable resin composition may be carried out at a temperature of 60°C to 90°C in one embodiment, 65°C to 85°C in another embodiment, and 70°C to 80°C in yet another embodiment. Once the components are thoroughly mixed to form the curable FR epoxy resin composition, the curable composition is ready to be cured, and prior to curing the composition, a fibrous structure such as a woven fabric mat or other structural material may be injected or impregnated into the FR curable epoxy resin composition to form an epoxy-based resin composite prepreg, which may be cured to form a composite article as described herein below.

[0056] The curable FR epoxy resin composite composition of the present invention has several beneficial properties and performance, especially when the appropriate components are mixed together to form a die-curable epoxy resin composition. For example, some advantages of using the curable epoxy resin composition of the present invention include the following advantages when compounds that constitute the components of the curable composition, such as FR agents and IMR agents, are used: (1) the FR agents and IMR agents can be easily incorporated into the epoxy resin formulation without significantly increasing the viscosity of the resin blend, (2) the IMR agents help to release the molded composite from the molding tool during molding at high temperatures (e.g., above 145°C), (3) the IMR agents help to release the molded composite with a cure cycle time of less than 5 minutes, (4) the IMR agents help to release the die-cured epoxy resin from the mold that cures within 5 minutes, and (5) the FR agents, IMR agents, and reaction inhibitors do not reduce the Tg of the cured composite part by more than 10%. Furthermore, the epoxy composite article of the present invention can be achieved by compounding the epoxy composite formulation of the present invention with a diamide curing agent, and isothermally molding and curing at a temperature above 140°C.

[0057] The FR agent used in the present invention does not substantially increase the viscosity of the epoxy resin composition. For example, the viscosity of the resin composition at 110°C may be 1 Pa.s to 15 Pa.s in one embodiment, 1 Pa.s to 12 Pa.s in another embodiment, and 1 Pa.s to 10 Pa.s in yet another embodiment. The viscosity of the resin composition may be measured with a rheometer according to a standard dynamic temperature ramp measurement procedure.

[0058] The curable FR epoxy resin composition is described above. Once the FR epoxy resin composition is prepared, it can be contacted with a reinforcing fiber substrate, for example, by injecting or impregnating the reinforcing fiber substrate with the resin composition to form a prepreg article.

[0059] An inventive prepreg product produced with the inventive curable FR epoxy resin composition includes, for example, (i) a reinforcing fiber substrate; and (ii) a curable FR epoxy resin composition as described above that has been impregnated into the reinforcing fiber substrate to form an uncured or partially cured prepreg including the FR epoxy resin composition and the reinforcing fiber substrate integrally integrated therewith.

[0060] The above FR epoxy resin composition of the present invention can be combined with a wide variety of different reinforcing fibers (or fibrous materials in the form of linseed or woven fabrics). The reinforcing fibers used in the present invention can include, for example, carbon fibers, graphite fibers, glass fibers, aramid fibers, silicon carbide fibers, polyester fibers, ceramic fibers, alumina fibers, boron fibers, metal fibers, mineral fibers, ore fibers, slag fibers, natural fibers (such as basalt, hemp, seaweed, hay, flax, straw, jute, or coconut), and mixtures thereof. In one preferred embodiment, the reinforcing fibers can be selected from the group consisting of carbon fibers, glass fibers, aramid fibers, and mixtures thereof.

[0061] The fibers may have a diameter, for example, from 250 nanometers (nm) to 500 μm in one general embodiment, from 500 nm to 50 μm in another embodiment, and from 1 μm to 10 μm in yet another embodiment.

[0062] The fibers can be continuous. The continuous fibers can be, for example, unidirectional, woven, knitted, braided, or mechanically entangled. Alternatively, the fibers can be chopped, for example, short fibers having lengths of up to 100 millimeters (mm) in one embodiment, and 3 mm to 50 mm in another embodiment. The chopped fibers can be held together with a binder to form a fiber mat. In certain embodiments, the fibers can be randomly oriented chopped fibers having lengths of 12 mm to 25 mm.

[0063] Generally, the fiber content of the composite composition may range from 5% to 80% by weight in one embodiment, from 20% to 80% by weight in another embodiment, and from 35% to 70% by weight in yet another embodiment of the total weight of the composition. In one preferred embodiment, the fiber content of the composite composition may be, for example, 60% by weight.

[0064] In a broad embodiment, a process for producing a prepreg of the invention includes, for example, the following steps: (a) providing a curable FR epoxy resin composition as described above; (b) providing a woven carbon fiber substrate as described above; (c) contacting, for example, by injecting (or impregnating) the woven carbon fiber substrate with the FR epoxy resin composition; and (d) heating the woven carbon fiber substrate containing the FR epoxy resin composition of step (c) sufficient to form an uncured or partially cured prepreg.

[0065] The infusion or impregnation step (c) of the process, and generally the preparation of the prepreg, can be accomplished using conventional prepreg formation methods and equipment. In general, the prepregs of the present invention can be produced by infusing (or impregnating) a fibrous material (or woven fiber fabric substrate) with the FR epoxy resin composition.

[0066] In one embodiment, the infusion of the epoxy resin composition into the fibrous material is carried out at a temperature ranging from 90°C to 130°C, in another embodiment from 100°C to 125°C, and in yet another embodiment from 110°C to 125°C. It should be appreciated that temperature ranges outside the above ranges can also be used. However, the use of higher or lower injection temperatures typically requires adjustment of the machine speed at which the infusion process is carried out. For example, at temperatures above about 125°C, it may be necessary to carry out the infusion process at a higher machine speed to reduce the time that the epoxy resin composition is exposed to the high temperature to avoid undesired crosslinking of the epoxy resin composition. Similarly, the use of a lower injection temperature will typically require a lower machine speed for infusing the epoxy resin composition into the fibrous material to obtain a desired level of infusion, thereby reducing voids in the prepreg. In one preferred embodiment, the epoxy resin composition can be applied to the fibrous material at a temperature in the above range, and the epoxy resin composition can be hardened into the fibrous material by pressure. For example, the pressure applied to the combination of the fibrous material and the resin can be applied by passing the combination through one or more pairs of nip rollers.

[0067] Generally, the process of preparing prepregs useful in the present invention includes a first step of, for example, extruding an epoxy resin composition onto a sheet material to form a film resin coating on the sheet material. The sheet material can be a release film or paper from which the film coating of the epoxy resin composition can be transferred to a fibrous material during the formation of the prepreg article (i.e., the prepreg process). After the film of the epoxy resin composition is deposited on the sheet material, the sheet material with the film resin coating can be passed through a chill roll to cool the epoxy resin composition. The sheet material of the epoxy resin composition can then be wound into a roll for future use.

[0068] In a second step of the process, the sheet material having the epoxy resin composition film coating can be contacted with a surface of a fibrous material (e.g., NCF, braid, or unidirectional woven fabric). Pressure can then be applied to the sheet material having the epoxy resin composition film coating to infuse the epoxy resin into the fibrous material. Preferably, the fibrous material and the sheet material containing the epoxy resin composition are provided as continuous tapes from respective supply rolls.

[0069] In a preferred embodiment, a sheet of fibrous material can be sandwiched between two sheets of material on which a film coating of the epoxy resin composition has been deposited. The sandwiched materials can then be heated to increase the temperature of the epoxy resin composition. In one embodiment, this heating can be accomplished by passing the combination of fibrous material and epoxy resin composition through a heated plate. For example, the epoxy resin composition can be heated to a temperature of about 120° C. to facilitate rapid infusion of the epoxy resin composition into the fibrous material. The combined sheet of resin and fibrous material can then be passed through a pair of nip rolls that press the epoxy resin composition against opposing surfaces of the fibrous material.

[0070] In a preferred embodiment, the combination of fibrous material and epoxy resin composition can be subjected to a second step of passing the combination through a hot plate and then passing the combination through a second nip to further infuse the epoxy resin composition into the fibrous material to form a resin-infused prepreg. The prepreg can then be cooled, for example, by passing the material through a chill roll or chill plate. After cooling, the prepreg can be wound onto a supply roll for future use.

[0071] In one preferred embodiment, the release paper or film on which the epoxy resin composition is coated as a resin film can be rewound onto a roll following a step of cooling the epoxy resin composition. As mentioned above, the infusion step can be performed at an elevated temperature to reduce the viscosity of the epoxy resin composition. In addition, the infused epoxy resin composition can be subjected to a partial curing step (advancing) to increase the glass transition temperature of the epoxy resin composition in the prepreg. The prepreg can then be packaged, stored, or shipped as required. As mentioned above, in some embodiments, it may also be desirable to subject the prepreg to an advancing step to increase the Tg of the epoxy resin, thereby reducing the tack of the prepreg.

[0072] In addition to having FR properties, the prepreg of the present invention has several beneficial properties and performances. For example, the prepreg may exhibit low tack or may be "tack-free", as determined by touching the prepreg after it is produced, and the tactile properties of the prepreg do not feel sticky. The tack-free properties of the prepreg may also be determined by observation, for example, by observing that the prepregs do not stick to each other when two or more prepreg layers are stacked on top of each other.

[0073] In a first broad embodiment, the flame retardant carbon fiber composite of the invention can be a fully (or fully) cured composite formed by impregnating the fibrous substrate with a curable FR epoxy resin composition immediately followed by fully curing the impregnated fibrous substrate. In a second broad embodiment, the flame retardant carbon composite of the invention can be a fully (or fully) cured composite formed by first producing a partially cured tack-free prepreg as described above, and then continuing to cure the tack-free prepreg until the prepreg is fully cured. In the second broad embodiment, for example, the process for making the composite generally includes the following steps: (I) providing at least one supporting structural substrate, (II) providing a curable FR epoxy resin composition as described above, (III) impregnating the substrate with the epoxy composition, (IV) heating (advancing) the impregnated substrate of step (III) sufficient to form a tack-free prepreg, and (V) curing the tack-free prepreg at a temperature sufficient to fully cure the prepreg.

[0074] In one embodiment, the curing step can be carried out at an isothermal molding temperature that is greater than 140° C. in one embodiment, greater than 145° C. in another embodiment, greater than 150° C. in yet another embodiment, and greater than 160° C. in yet another embodiment. Other embodiments of the curing temperature can be, for example, between 140° C. and 170° C. in one embodiment, and between 145° C. and 160° C. in another embodiment.

[0075] The carbon fiber composite material of the present invention has several beneficial properties and performances, including, for example, high flame retardancy. For example, the flame retardancy of the carbon fiber composite material may be sufficient to pass a flame retardancy test and obtain a UL94 classification of at least V-1 in one embodiment, and a UL94 classification of V-0 in another embodiment. The flame retardancy of the carbon fiber composite material may be measured by the UL94 standard for plastic material flammability testing for equipment and appliance parts (flammability standard for plastics released by Underwriters Laboratories in the United States). Advantageously, in a preferred embodiment, the composite material of the present invention exhibits a flame retardancy that passes the UL94 V-1 classification.

[0076] The composite article of the present invention has several other advantageous properties. For example, the composite material may have a high glass transition temperature (Tg) of greater than 140°C in one embodiment, between 140°C and 170°C in another embodiment, and between 150°C and 170°C in yet another embodiment. The Tg of the composite material may be measured as described in ASTM D5418-15. Some examples of several other advantageous properties exhibited by the composite article may include exhibiting a Tg greater than 150°C and being able to demold at mold temperatures greater than 145°C with a cure time of less than 3 minutes.

[0077] In a preferred embodiment, the glass transition temperature of the cured part is not reduced by more than 10% when using the formulation of the present invention with the FR agent disclosed herein, as illustrated by the following formula: ΔTg=Tg w / oFRagent -Tg w / FRagent (In the formula, Tg w / oFRagent is the glass transition temperature of the blend without the FR agent present in the blend, and Tg w / FRagent is the glass transition temperature of the formulation with the IMR agent and the reaction inhibitor present in the formulation).

[0078] The carbon fiber composite material of the present invention can be used in applications where the flame retardant properties of the composite material are beneficial. For example, in a preferred embodiment, the fiber composite material of the present invention can be used to manufacture housings for lithium batteries. EXAMPLES

[0079] The following examples are presented to further illustrate the invention, but should not be construed as limiting the scope of the claims. All parts and percentages are by weight unless otherwise indicated.

[0080] The various raw materials (ingredients or components) used in the following inventive examples (Inv. Ex.) and comparative examples (Comp. Ex.) are set out in Table I herein below. [Table 1]

[0081] General Procedure for Preparing Epoxy Compositions Samples of epoxy resin formulations were prepared by first heating 100 grams (g) of resin(s) to 90° C. in a 20Max mixer cup (FlackTek Inc.). The amounts of FR agent, IMR agent, Technicure Nanodicy, and accelerators listed in Tables II and III were added to the resin while it was hot, and the resulting hot mixture was immediately placed in a SpeedMixer™ Laboratory Mixer System (FlackTek Inc.). The mixture of components was mixed at 3,000 revolutions per minute (RPM) until the mixture was visually homogenous (1-2 min). The resulting sample mixture was then examined by DSC and other property measurements as described above.

[0082] General procedure for preparing clear casts Using the above epoxy resin composition, epoxy clearcast plaques were prepared by compression molding using a Wabash MPI platen press (G302H-18-CLX). A 15 centimeter (cm) x 15 cm x 0.32 cm mold was used to prepare the plaques. The epoxy resin was poured into the mold and the resin was cured for 10 minutes in a heated platen press at 150°C.

[0083] General procedure for preparing composite materials The prepared resin mixture was first filmed on one side of a release paper with an appropriate thickness. Once the resin system cooled to room temperature, it became tack-free, so the resin film on the release paper could be rolled up and stored until future use. To produce the prepreg, the selected fiber structure was sandwiched between two layers of filmed resin and passed through a prepreg line that included a heated table that melted the epoxy resin and a compression roller that pressed the molten epoxy resin onto the opposite surface of the fabric. After the prepreg passed through the heated rollers and chiller plate, the prepreg was rolled up. The rolls of prepreg were stored at ambient temperature (approximately 25°C).

[0084] The carbon fiber fabric used was obtained from A&P Technology and had a weight of 340 grams per square meter (g / m 2 ) stitched unidirectional (UD) woven fabric. Flat panel composite laminates were compression molded from square prepregs. The size dimensions of the square prepregs were 30.5 cm x 3.5 cm. Molding conditions were as follows: platen temperature 150°C, 15 seconds to close the tool, 2 megapascals (MPa) to 3.5 MPa for 15 seconds, 2.5 second ramp to 17 MPa for 300 seconds.

[0085] Test Method Viscosity of the epoxy composition Viscosity versus temperature measurements were performed on a TA Instruments ARES rheometer. Dynamic temperature ramp measurements were performed at a ramp rate of 10°C / min using a disposable cup and plate geometry (25 mm diameter) in the temperature range of 40°C to 200°C.

[0086] Analytical evaluation of compression molded flat plaques. Dynamic mechanical analysis (DMA) testing was used to determine the glass transition temperature (Tg) of the molded materials. The Tg values ​​of the final molded parts were determined by the method described in DMA-ASTM D5418-15 (2015). The fiber content, resin content, and porosity of the composites were determined using ASTM D3171 (Procedure G, Matrix Burn-off in a Muffle Furnace).

[0087] Flame retardants The UL94 standard was used on a group of five 13mm x 125mm sample specimens. After equilibrating in a laboratory environment at 23°C ± 2°C and 50% relative humidity for at least 24 hours (hours), the specimens were mounted vertically in a test fixture. A 20mm high flame was applied to the bottom edge of the specimen for two 10 second periods. The time the specimen continued to burn after the flame was applied was measured. If the sample burned completely, the specimen was not given a UL rating. If the longest burn time on any one specimen was less than 30 seconds and the total burn time when both flames were applied to all five specimens was less than 250 seconds, the material was given a ULV-1 rating. If the longest burn time on any one specimen was less than 10 seconds and the total burn time when both flames were applied to all five specimens was less than 50 seconds, the material was given a ULV-0 rating.

[0088] Examples 1 to 4 and Comparative Examples A to D The data in Table II show that the present invention can provide the required balance of glass transition temperature (Tg) and flame retardancy with only a small increase in viscosity. Comp.Ex.A is a resin containing no FR agents. Inv.Ex.1 and Inv.Ex.2 contain two different levels of flame retardant, 23% and 9% by weight, respectively, which corresponds to 5.5% and 2.2% by weight phosphorus, respectively. [Table 2]

[0089] Both clear cast specimens containing FR agent (Inv.Ex.1 and Inv.Ex.2) achieved V-0 rating in UL94V flame test. In carbon fiber prepreg manufacturing, resin viscosity needs to be low (e.g., less than 10 Pa.s at injection temperature) to facilitate injection into carbon fiber fabric. Higher resin viscosity can result in defects and dry areas in the composite. Addition of fillers to epoxy matrix resins generally tends to significantly increase resin viscosity, especially at higher filler loading levels. A balance between processing and improved flame retardancy is required when using the particulate addition approach. As can be seen, the addition of 23 wt% FR agent significantly increased the resin viscosity at injection temperature, while only a slight increase in viscosity was observed in Inv.Ex.2.

[0090] A composite sample (Comp.Ex.B) was prepared from the epoxy resin composition of Comp.Ex.A and a composite sample (Comp.Ex.C) was prepared from the epoxy resin composition of Inv.Ex.2 as described in Table II. A direct comparison of the flame retardancy and Tg results of these two composites (Comp.Ex.B and Comp.Ex.C) is shown in Table III. All composites were prepared using 340 grams / m2 of reinforcement. 2 Made of stitched UD carbon fiber fabric.

[0091] Addition of 9 wt% Exolit OP 945FR agent to the epoxy composition gave the neat composition (Inv.Ex.2) a UL94 V-0 rating, as listed in Table II, while the corresponding composite (Comp.Ex.C) failed to obtain a favorable rating in the UL94V flame test, as listed in Table III. Increasing the EXOLIT OP 945 content to 13 wt% (Inv.Ex.3) significantly improved the flame retardancy of the system, with the composite achieving a V-1 rating. Inv.Ex.3 achieved a V-1 rating with a phosphorus (P) content of only 0.9 wt% of the total composite weight (resin + fiber weight). Further increase in the EXOLIT OP 945 content to 16.7 wt% (1 wt% P content) gave the composite Inv.Ex.4 a V-0 rating. Even at this high loading of flame retardant (16.7 wt%), the glass transition temperature of the composite was only reduced by about 10%.

[0092] During the infusion of the resin composition into the reinforcing material to produce the fiber reinforced composite material, the particulate materials (depending on their size) can be retained and filtered by the fiber mat at the inlet of the resin. Generally, particles with a size above 5 μm tend to be filtered by the carbon fiber fabric. The particle size of Exolit OP 945 FR agent is advantageously small (size less than 5 μm). On the other hand, Comp.Ex.D also contains FR agent, but with a larger particle size of 15 μm. As can be seen from the data in Table III, Even at a much higher %P content, the Comp.Ex.D composite failed to achieve the standard in the UL94V flame test. [Table 3]

[0093] Table IV compares the mechanical properties of the Inv.Ex.4 composite, which contains the highest level of FR agent (16.7 wt%), with the Comp.Ex.B composite, which contains no FR agent in the composite. No degradation in the mechanical properties of the molded composite parts was observed with the addition of high levels of FR agent. [Table 4]

[0094] The epoxy resin compositions of the present invention (Inv.Ex.3 and Inv.Ex.4) resulted in tack-free prepregs that are very suitable for automated handling. The epoxy resin compositions cure extremely quickly, being fully cured in 3 minutes when compression molded at 150°C. The resulting epoxy carbon fiber composite has a Tg above 150°C. Due to the Tg of the composite, parts made with this composite and compression molded at about 150°C can be released without warping while still hot. That is, the Tg allows the part to be fully and completely demolded without first cooling the mold and part, thus reducing the molding cycle time. The molded composite plaques show low porosity of less than 2% as shown above, indicating the excellent infusibility of the resin system.

[0095] Other embodiments One preferred embodiment of the present invention described above includes a flame retardant epoxy resin prepreg, particularly a prepreg that may be advantageously tack-free. The prepreg includes (I) at least one support structure including a fiber reinforced substrate, the at least one support structure being a carbon fiber reinforcement or a glass fiber reinforcement, and in one embodiment, the fiber reinforcement may be a woven fabric. The prepreg also includes (II) the above curable flame retardant epoxy resin composition impregnated into the substrate.

[0096] Another preferred embodiment of the invention as described above includes a process for making the prepreg as described above, comprising the steps of: (I) providing at least one supporting structural substrate, (II) providing the curable flame retardant epoxy resin composition as described above, (III) impregnating the substrate with the curable flame retardant epoxy resin composition, and (IV) heating the impregnated substrate of step (III) sufficient to form a tack-free prepreg.

[0097] Yet another preferred embodiment of the present invention as described above includes a flame retardant cured composite comprising the cured flame retardant epoxy resin composition of claim 1, having flame retardancy that at least meets the UL94 V-1 standard classification, or that meets the UL94 V-0 standard classification. The composition can be produced by curing the tack-free prepreg as described above.

[0098] Yet another preferred embodiment of the present invention includes a process for making a composite material, comprising curing the above curable flame retardant epoxy resin composition at a cure temperature of, for example, 145°C to 160°C. The present invention includes the following aspects. Section 1. 1. A curable flame retardant epoxy resin composition comprising: (a) at least one epoxy resin selected to provide a tack-free prepreg; (b) at least one non-halogenated phosphorus-containing flame retardant to provide a fiber reinforced epoxy resin composite that exhibits flame retardancy of at least UL94 V-1 standard while retaining its mechanical properties; and (c) at least one release agent; (d) at least one hardener; and (e) at least one catalyst. Section 2. Item 2. The fiber-reinforced epoxy resin composite exhibits flame retardancy of at least UL94 V-1 standard, while maintaining a tensile strength in the range of 1,000 MPa to 2,500 MPa and a stiffness in the range of 100 GPa to 200 GPa. The composition according to item 1. Section 3. Item 1, wherein the at least one epoxy resin component (a) is an oxazolidone-based epoxy resin, the at least one non-halogenated phosphorus-containing flame retardant is aluminum diethylphosphinate, the at least one mold release agent is an ester of polyol and montanic acid, the at least one curing agent is dicyandiamide, and the at least one catalyst is a urea compound selected from one or more of toluene bis-dimethylurea, p-chlorophenyl-N,N dimethylurea, 3-phenyl-1,1-dimethylurea, 3,4-dichlorophenyl-N,N-dimethylurea, N-(3-chloro-4-methylphenyl)-N',N'-dimethylurea, and mixtures thereof. Section 4. Item 1. The composition according to item 1, wherein the epoxy resin composition maintains a tensile strength in the range of 1,000 MPa to 2,500 MPa and a rigidity in the range of 100 GPa to 200 GPa, while the fiber-reinforced epoxy resin composite material has a flame retardancy of UL94 V-0 standard. Section 5. Item 1. The composition according to item 1, wherein the flame retardant has an average particle size of less than 5 microns to avoid particulate filtration by carbon fiber reinforcement. Section 6. Item 1, wherein the epoxy resin composition is tack-free at about 22 ° C, cures at 150 ° C within 3 minutes, and provides a carbon fiber composite material having a cured glass transition temperature of greater than 150 ° C and a cured composite material achieving UL94 V-1 classification. The composition according to item 1 provides an epoxy fiber prepreg. Section 7. Item 1, wherein the concentration of the at least one epoxy resin is 80 weight percent to 90 weight percent, the concentration of the at least one non-halogenated phosphorus-containing flame retardant is 1 weight percent to 30 weight percent, the concentration of the at least one release agent is 2 weight percent to 5 weight percent, the concentration of the at least one curing agent is 6 weight percent to 8 weight percent, and the concentration of the at least one catalyst is 2 weight percent to 5 weight percent. Section 8. 1. A process for making a curable flame retardant epoxy resin composition comprising: (a) at least one epoxy resin; (b) at least one non-halogenated phosphorus-containing flame retardant to provide a fiber reinforced epoxy resin composite that exhibits flame retardancy of at least UL94 V-1 standard while retaining its mechanical properties; and (c) at least one release agent; (d) at least one hardener; and (e) mixing at least one catalyst. Section 9. A flame-retardant epoxy resin prepreg, (I) at least one support structure comprising a fiber-reinforced substrate; (II) The curable flame-retardant epoxy resin composition according to item 1 impregnated into the substrate. Section 10. 1. A process for making a prepreg, comprising: (I) providing at least one supporting structure substrate; (II) providing a curable flame retardant epoxy resin composition according to item 1; (III) impregnating the substrate with a curable flame retardant epoxy resin composition; (IV) heating the impregnated substrate of step (III) sufficiently to form a tack-free prepreg. Section 11. Item 1. A flame-retardant cured composite material comprising the cured flame-retardant epoxy resin composition according to item 1, having flame retardancy that meets at least the UL94 V-1 standard classification.

Claims

1. (a) at least one epoxy resin comprising an oxazolidone-based epoxy resin; (b) at least one non-halogenated phosphorus-containing flame retardant comprising a phosphinate; and (c) at least one release agent; (d) at least one curing agent; (e) at least one catalyst, Based on the total weight of the curable flame retardant epoxy resin composition, the epoxy resin (a) is 66.4 to 78.6 wt % and the non-halogenated phosphorus-containing flame retardant (b) is 10 to 20 wt %; the non-halogenated phosphorus-containing flame retardant (b) having an average particle size of less than 5 microns.

2. the at least one epoxy resin (a) is an oxazolidone-based epoxy resin; the at least one non-halogenated phosphorus-containing flame retardant (b) is aluminum diethylphosphinate; the at least one mold release agent (c) being an ester of a polyol and montanic acid; the at least one curing agent (d) is dicyandiamide; the at least one catalyst (e) is a urea compound selected from one or more of toluene bis-dimethylurea, p-chlorophenyl-N,N-dimethylurea, 3-phenyl-1,1-dimethylurea, 3,4-dichlorophenyl-N,N-dimethylurea, N-(3-chloro-4-methylphenyl)-N',N'-dimethylurea, and mixtures thereof; 2. The curable flame retardant epoxy resin composition of claim 1.

3. 2. The curable flame retardant epoxy resin composition of claim 1, which provides an epoxy fiber prepreg that is tack-free at 22°C, cures at 150°C within 3 minutes, and is capable of providing a carbon fiber composite material having a cured glass transition temperature greater than 150°C and a cured composite material exhibiting flame retardancy of UL94 V-1 standard.

4. the concentration of said at least one release agent (c) is between 2 percent by weight and 5 percent by weight; the concentration of the at least one curing agent (d) is 6 weight percent to 8 weight percent; the concentration of the at least one catalyst (e) is from 2 weight percent to 5 weight percent; The composition of claim 1.

5. (a) at least one epoxy resin comprising an oxazolidone-based epoxy resin; (b) at least one non-halogenated phosphorus-containing flame retardant comprising a phosphinate; and (c) at least one release agent; (d) at least one curing agent; (e) at least one catalyst; and Based on the total weight of the curable flame retardant epoxy resin composition, the epoxy resin (a) is 66.4 to 78.6 wt % and the non-halogenated phosphorus-containing flame retardant (b) is 10 to 20 wt %; A process for making a curable flame retardant epoxy resin composition, wherein the non-halogenated phosphorus-containing flame retardant (b) has an average particle size of less than 5 microns.

6. A flame-retardant epoxy resin prepreg, (I) at least one support structure comprising a fiber reinforced substrate; (II) the curable flame-retardant epoxy resin composition according to claim 1 impregnated into the fiber-reinforced substrate.

7. 1. A process for making a prepreg, comprising: (I) providing at least one supporting structural substrate; (II) providing a curable flame retardant epoxy resin composition according to claim 1; (III) impregnating the supporting structural substrate with the curable flame retardant epoxy resin composition; (IV) heating the impregnated supporting structure substrate of step (III) sufficiently to form a tack-free prepreg.

8. 10. A flame retardant cured composite material comprising the curable flame retardant epoxy resin composition of claim 1, which exhibits flame retardancy of at least UL94 V-1 standard.

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