This invention relates generally to composite materials, and, more specifically, to fiber-reinforced laminates.
Equipment such as aircraft commonly use aluminum alloys for structure and skin material. Because it is desirable to reduce weight of an aircraft, use of lightweight composite materials has also become common on aircraft. These lightweight composites include fiber metal laminates (FML). As an example, composite aluminum-fiber laminates and other metal-fiber laminates have been developed utilizing carbon and glass fiber layers interspersed between layers of aluminum or other metals. Low modulus fibers such as glass often may not have a sufficiently high modulus of elasticity to produce a laminate able to carry significant loads without potentially over-stressing or fatiguing the aluminum layers when the laminate is under repeated loading.
It would be desirable to use fibers having high strength characteristics, such as high modulus fibers. However, the use of high modulus fibers, such as graphite, in making fiber metal laminates often produces laminates with physical properties that are less than desirable for certain applications.
In one aspect, this invention is a fiber-metal laminate comprising: at least two metallic layers and at least one fiber layer disposed between the metallic layers; wherein the fiber layer contains a resin matrix and organic polymeric fibers having a modulus of elasticity of at least 270 GPa.
In another aspect, this invention is a fiber-metal laminate comprising: at least two layers of an aluminum alloy; and at least one resin-fiber ply bonded between the aluminum alloy layers, the ply including a resin matrix and poly diimidazo pyridinylene fibers.
In a third aspect, this invention is a composite aircraft component comprising: at least two aluminum alloy foil layers each having a thickness of at least 0.004 inches and no greater than 0.025 inches; and at least one polymeric composite layer bonded between the at least two foil layers, the composite layer including a resin matrix and aligned poly diimidazo pyridinylene fibers.
In a fourth aspect, this invention is a method for producing a fiber-metal laminate, the method comprising: providing a plurality of metallic layers; aligning a plurality of polymer fibers having a modulus of elasticity of greater than 270 GPa into at least one fiber layer; and sandwiching the fiber layer between the plurality of metallic layers.
In a fifth aspect, this invention is a fiber-metal laminate produced according to a method comprising: providing a plurality of metallic layers; aligning a plurality of polymer fibers having a modulus of elasticity of greater than 270 GPa into at least one fiber layer; and sandwiching the at least one fiber layer between the plurality of metallic layers.
It has been discovered that the fiber-metal laminates, composite components and the method for making them of this invention advantageously provide laminates and components with physical properties and corrosion resistance that is particularly useful in aircraft applications. These and other advantages of the invention will be apparent from the description which follows.
The preferred and alternative embodiments of the present invention are described in detail below with reference to the following drawings.
By way of overview, exemplary embodiments of the present invention provide a fiber metal laminate. At least two metallic layers are provided and at least one fiber layer is bonded between the two metallic layers. The fiber layer suitably includes a resin matrix and organic polymeric fibers with a modulus of elasticity greater than 270 GPa.
In accordance with further aspects of the invention, the polymeric fibers may include poly diimidazo pyridinylene fibers. In accordance with other aspects of the invention, the metallic layers may include pre-treated aluminum alloy layers.
Referring to
By way of example and not limitation, in one presently preferred embodiment the metallic layers 24 include heat treatable aluminum alloy foil layers having a thickness of at least 0.004 inches and no greater than 0.025 inches. Greater thickness foil layers may also be utilized, as described further in connection with
Use of the metallic layers 24 in conjunction with the fiber layers 20 allows the use of fewer or no cross-plys, as opposed to pure fiber composite laminates, for structures and skins that are primarily under tensile loads. The metallic layers 24 carry stress about equally in all directions in the plane of the metallic layer 24, while the fiber layers 20 typically exhibit substantially higher strength in a direction generally parallel to the fibers 22 than in a direction oblique to the fibers 22. Metallic layers 24 in the laminate 10 also add benefits of electrical conductivity, a moisture barrier, resistance to weather, and damage tolerance. The metallic layers 24 exhibit greater resistance to sharp objects than a fiber layer 20 alone, and show visible impact damage when impacted by other objects. In
The fiber layers 20 preferably include very high modulus polymer fibers that are not galvanically reactive with aluminum. The high modulus fibers 22 carry most of the stress applied to the laminate 10, while minimizing over-stressing and fatigue to the metallic layers 24. The very high modulus non-reactive polymer fibers permit the laminate 10 to be only 10 percent to 40 percent metal by weight. At the same time, for example for areas such as structural joints where additional multidirectional stress carrying capacity for complex loading is desired, the laminate 10 may be 10 percent to 50 percent metal by volume.
In one preferred embodiment, the fiber layers 20 include a resin matrix (not shown) that holds the polymer fibers 22. The resin matrix is often a thermo-hardening material; permitting heat cure of the laminate. Exemplary resin matrixes include, by way of example and not limitation, thermal curing epoxies and resins such as TORAY™ 3900-2, CYTEC™ CYCOM™ 934, and HEXCEL™ F155; bismaleimide based adhesives such as CYTEC™ 5250-4; and Cyanate Esters such as STESALIT™ PN-900. The matrix resins typically may be heat cured. The resins may be formed with the fibers 22 into “pre-pregs”, that is pre-assembled pre-impregnated layers often including multiple layers of the fibers 22. Multiple pre-pregs (not shown) may form a fiber layer 20.
In one preferred embodiment of the present invention the laminate 10 includes very high modulus non-reactive polymer fibers 22 with moduli of elasticity over 270 GPa. Exemplary non-reactive fibers with very high moduli of elasticity include without limitation poly2,6-diimidazo[4,5-b4′,5′-e]pyridinylene-1,4(2,5-dihydroxy)phenylenes (“PIPD”), such as M5™ fiber, manufactured by Magellan Systems International, with a modulus of elasticity over 300 GPa. An alternate non-reactive very high elastic modulus polymer is poly (p-phenylene-2,6-benzobisoxazole) (“PBO”), such as ZYLON™, manufactured by Toyobo Co., Ltd of Osaka, Japan. The fibers 22 are typically assembled in alignment and embedded in a resin matrix to form fiber layers 20.
In a presently preferred embodiment, the metallic layers 24 are bonded to the fiber layers 20 during assembly of the laminate 10. The fiber layers 20 suitably may bond themselves to the metallic layers 24 when the laminate 10 is assembled and held under pressure during heat curing. However, bond strengths between the fiber layers 20 and the metallic layers 24 can be enhanced if desired, by way of example and not limitation, by pre-treatment of the metallic layers 24 and by using a separate adhesive between the metallic layers 24 and the fiber layers 20.
Suitable optional adhesives for increasing bond strength if desired between the fiber layers 20 and the metallic layers 24 include heat cured epoxies, such as without limitation Applied Poleramic, Inc., MSR-355 HSC™, and Applied Poleramic, Inc., MSR-351™. These epoxies (not shown) serve as an interphase adhesive between the fiber layers 20 and the metallic layers 24.
The metallic layers 24 themselves suitably may be pre-treated to increase adhesion to the fiber layers 20, thereby increasing the strength and durability of the laminate 10. Pre-treatments suitably may include a wide variety of metallic pre-treatments including acid or alkaline etching, conversion coatings, phosphoric acid anodizing, and the like. Such pre-treatments may increase surface roughness, thereby facilitating a stronger physical bond with the adhesive, or may facilitate a better chemical bond with the adhesive. In one presently preferred embodiment, a further alternate pre-treatment of applying a sol-gel coating to the metallic layers 24 may be utilized prior to assembly of the laminate 10. The sol-gel process commonly uses inorganic or organo-metallic pre-cursors to form an inorganic polymer sol. Sol-gel coatings include zirconium-silicone coatings, such as those described in Blohowiak, et al., U.S. Pat. Nos. 5,849,110; 5,869,140; and 6,037,060, all of which are hereby incorporated by reference. The resulting inorganic polymer sol coating serves as an interphase layer between the metal layers 24 and the fiber layers 20 when they are bonded together. Pre-treatments may also include grit blasting. Grit blasting may also suitably cold work the alloys in the metallic layers 24. Further exemplary pre-treatments suitably may include heat treatment and wet honing.
It will be appreciated that including the metallic layers 24 in the laminate 10 permits all of the fibers 22 of the fiber layers 20 to be in alignment. Typically in composites that do not include the metallic layers 24, a 10 percent-90° rule is applied. As is known, this means that in a composite, approximately 10 percent of the fibers are oriented 90° to the primary axis of stress. The 10 percent of the fibers oriented at 90° to the primary axis of stress prevent disintegration in sheer of the composite. When the metallic layers 24 are combined with the fiber layers 20 such as the high elastic modulus, non-reactive polymer fibers 22, as low as 0 percent of the fibers 22 may be oriented at 90° to the primary stress. Thus, a laminate 10 with all of the fibers 22 aligned in a common direction advantageously may be assembled and utilized without the added materials and manufacturing steps of including cross-plys.
In a presently preferred embodiment, the laminate 10 is suitably assembled by first pre-treating the metallic layers 24 as described above, if desired. The fiber layers 20 are then interspersed between the metallic layers 24. Adhesive (not shown) is applied at each boundary between a metallic layer 24 and a fiber layer 20. The resulting stack is placed in a vacuum bag. The vacuum bag is placed into an autoclave. A vacuum is applied to the vacuum bag, and the autoclave is pressurized. The autoclave is heated to and held for a sufficient amount of time at a temperature suitable to activate and cure the adhesive (not shown) and the resin matrix (not shown) thereby curing the laminate 10. It will be appreciated that the temperatures and hold times for the autoclave correspond to those suitable for cure of the adhesive (not shown) and the resin matrix (not shown). In an exemplary embodiment, where TORAY™ 3900-2 with a 350° F. cure resin is utilized for the resin matrix (not shown), the autoclave is heated to approximately 350° F. and held at that temperature for approximately 120 minutes. Typical cure temperatures for heat curing resin adhesives and matrix resins include cures between 250° and 350° F.±10° for approximately two hours. It will be appreciated that heat curing of the adhesive (not shown) in the matrix resin (not shown) may also simultaneously heat treat or heat age the metallic layers 24.
It will also be appreciated that during forming, the laminate 10 may be formed over a form or in a complex shape prior to cure. This permits the laminate 10 to be formed and cured into curved or segmented shapes such as a curved section described below in connection with
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It will be appreciated that, multiple fiber layers 50 may be positioned between two metallic layers 54, thereby increasing the ratio of fiber layers 50 to metallic layers 54. Referring now to
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For some applications it may be advantageous for one or more of the metallic layers of the laminate to be thicker than the other layers. In
It will be appreciated that a hollow core layer may be incorporated into a high modulus fiber-metal laminate. Referring now to
The high modulus fiber laminate of the present invention may be incorporated into aircraft components. Referring now to
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While the preferred embodiment of the invention has been illustrated and described, as noted above, many changes can be made without departing from the spirit and scope of the invention. Accordingly, the scope of the invention is not limited by the disclosure of the preferred embodiment. Instead, the invention should be determined entirely by reference to the claims that follow.