• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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    • 专利摘要:
    1 / 1 abstract “shell layer system, methods for surface preparation of various composite substrates and for forming a composite structure bonded†a layer resin-rich shell (11) that does not leave behind residual fibers after detachment and can work well with different resin-based composite substrates (10). the resin-rich bark layer (11) is composed of a woven cloth (11b) impregnated with a resin matrix (11a) different from the resin matrix of the composite substrate (10). the bark layer (11) is designed such that, after manually removing the bark layer (11) from the surface of the composite substrate (10), a thin film of the bark layer resin remains on the surface. surface of the composite substrate to create a bondable surface capable of bonding with another composite substrate (12), however no fibrous material of the woven cloth remains on the same surface.
    公开号:BR112014012123B1
    申请号:R112014012123-0
    申请日:2012-11-16
    公开日:2020-08-11
    发明作者:Yiqiang Zhao；Dalip Kumar Kohli；Kunal Gaurang Shah
    申请人:Cytec Technology Corp；
    IPC主号:
    专利说明:

    BACKGROUND
    [0001] The present disclosure relates generally to layers of porous fabric for surface preparation of composite substrates, more particularly resin-based composite substrates, prior to bonding.
    [0002] Hand sanding, sandblasting and peel layer removal are conventional methods for preparing resin-based composite substrate surfaces for bonding adhesives in the aerospace industry. Adhesive bonding by peel removal is the most common of the three techniques because it saves significant amounts of labor and creates a more uniformly treated surface. Peel layer removal typically involves applying a dry, textured cloth material to the bonding surface of the resin-based composite substrate followed by curing. After curing, the shell layer is removed, that is, detached, to reveal a rough or textured bonding surface. However, dry peelplies tend to leave broken broken fibers on the bonding surface after shedding. This leads to poor adhesive bonding properties because residual fibers can act as defects that prevent the adhesive from fully wetting the bonding surface of the composite substrate, thereby resulting in adhesive failure. The general experience in the industry is that the shell layer process lacks predictability and reliability with respect to bonding performance. SUMMARY
    [0003] The present disclosure provides a resin-rich shell layer that leaves no residual fibers behind after shedding and can work well with different resin-based composite substrates. The resin-rich shell layer is composed of a woven cloth impregnated with a resin matrix different from the resin matrix of the composite substrate. The shell layer is designed in such a way that, after manually removing the shell layer from the surface of the composite substrate, a thin film of the shell layer resin remains on the surface of the composite substrate to create a bondable, but no fibrous material from the woven cloth remains on the same surface. This resin-rich shell layer is capable of modifying the surface of various composites for secure bonding with a variety of adhesives. Consequently it could be considered as a “universal” shell layer.
    [0004] The present disclosure also provides a method of preparing a surface for bonding composite using the shell layer discussed above. Also disclosed is a method of forming a bonded composite structure that includes: applying a layer of bark to a surface of a first composite substrate composed of fiber-reinforced resin; cure the shell layer and the first composite substrate together; removing the shell layer from the first composite substrate leaving behind a thin layer of shell layer resin on the surface of the composite substrate; applying an adhesive film to at least one of the modified surface of the first composite substrate and a surface of a second composite substrate; contacting the modified surface of the first composite substrate with a surface of the second composite substrate with the adhesive film between them; and cure to bond the substrates. BRIEF DESCRIPTION OF THE DRAWINGS
    [0005] Figure 1 shows schematically the working mechanism of the resin-rich shell layer according to the present disclosure.
    [0006] Figure 2 shows the fracture line that occurs when the shell layer is removed from a composite substrate.
    [0007] Figure 3 is a scanning electron microscope (SEM) image of an exemplary polyester cloth that can be used for the resin-rich shell layer.
    [0008] Figure 4 is a scanning electron microscope (SEM) image of an exemplary glass cloth that can be used for the resin-rich shell layer.
    [0009] Figure 5 is a scanning electron microscope (SEM) image of a treated surface after the resin-rich shell layer is removed.
    [0010] Figure 6 shows the data of fracture toughness (Gic) for several prepregs bonded in an Example.
    [0011] Figures 7A and 7B are optical microscope images showing the cohesive failure condition of linked prepregs after fracture toughness test (Gic) according to an Example. DETAILED DESCRIPTION
    [0012] It has been discovered that an advantage that can be realized in treating a fiber-reinforced resin composite substrate with a resin-rich shell layer to modify the treated composite substrate surface in order to facilitate and promote bonding duration longer and stronger between the surface-treated composite structure and a second composite substrate. The surface of the composite substrate (10) is modified by a thin resin film (12) that remains on it after the resin-rich peel layer (11) is detached (figure 1). The working mechanism of the shell layer is illustrated in figure 1. The thickness of the remaining resin after the shell layer has been removed is approximately 2% - 15% of the original thickness of the shell layer before peeling off. This remaining peel layer resin layer provides a compatible surface layer for bonding adhesive, including joint bonding and secondary bonding. Bonding together in the composite bonding industry means bonding a cured prepreg to an uncured prepreg using adhesive. Secondary bonding means bonding a cured prepreg with another cured prepreg using adhesive. The rheology and curing kinetics of the shell layer resin are controlled to minimize intermixing between the shell layer resin and the composite substrate resin during curing, so the shell layer resin formulation has substantially curing kinetics faster than the resin formulation of the composite substrate. As the resin-rich shell layer can be used with various fiber-reinforced resin composite substrates, it can be considered as a “universal” shell layer.
    [0013] The fiber reinforced resin composite substrates discussed here include prepregs or prepreg layups conventionally used in the manufacture of aerospace structural parts. The term "prepreg" as used here refers to the fiber sheet or sheet that has been impregnated with a matrix resin. The matrix resin can be present in an uncured or partially cured state. The term "prepreg layup" as used here refers to a plurality of prepreg layers that are layers adjacent to each other in a stack. The prepreg layers in the layup can be positioned in a selected orientation in relation to each other. For example, prepreg layups can comprise layers of prepreg having unidirectional fiber architectures, with the fibers oriented at 0o, 90 °, a selected angle 0, and combinations thereof, with respect to the largest dimension of the layup, such as length. It should be further understood that, in certain modalities, prepregs can have any combination of fiber architectures, such as unidirectional and multidimensional.
    [0014] The resin-rich shell layer (11) of the present disclosure is composed of a woven cloth (Ha) impregnated by a resin matrix (11b), as shown in figure 1, and has a resin content of at least 20% by weight based on the total weight of the shell layer, depending on the specific type of woven cloth being impregnated. In certain embodiments, the resin content is in the range of 20% - 50%. The resin formulation and cloth construction are selected in such a way that no broken fibers are left on the surface of the composite substrate after the peel layer has been removed. The fracture line (13) during detachment is comprised in the resin matrix (11b) or in the resin-fiber interface, but not in the cloth (11a), as shown in figure 2. The resin-rich shell layer is easily removed the surface of the composite substrate after curing. For this purpose, it has a release resistance of no more than 10 in-lb / inch in width - according to the ASTM D1781 Drum Release Test.
    [0015] The resin-rich bark layer cloth is composed of a plurality of threads woven in a weave pattern. Each strand is composed of a plurality of continuous fibrous filaments (single fibers) twisted together. The woven cloth has a cloth weight in the range of 50-250 gsm (grams / m2), preferably 70-220 gsm, and a thickness in the range of 50-250 pm, preferably 100-200 pm. thickness is mainly a function of weight and type of fiber, but it also depends on the weave. The type of fiber for the woven cloth can be selected from various synthetic materials including polyesters (polyethylene terephthalate, polybutylene terephthalate, polyitrimethylene terephthalate, polylactic acid, and copolymers thereof), polyethylene, polypropylene, nylon, elastomeric materials such as LYCRA® ; high-performance fibers such as polyamides (eg Kevlar), polyimides, polyethylene imine (PEI), polyoxazole (eg Zylon), polybenzimidazole (PBI), polyether ether ketone (PEEK) and glass. The main requirements for the fiber material are: the material is not brittle and has the required tensile strength. In addition, the cloth may have a heat-curing finish or other conventional finishes.
    [0016] Yarn size can be expressed in terms of units of denier linear mass density. Denier is equal to the weight in grams of 9000 meters of yarn. The lower the number, the thinner the thread. For a roll of cloth, the threads that extend in the direction of the roll and are continuous for the entire length of the roll are the warp threads. The short strands extending across the roll direction are called the filler strands. For the resin-rich bark layer, the cloth is selected based on the following characteristics: warp yarns with linear mass density in the range of 50-250 deniers, preferably 70-230 deniers, and filler yarns with linear mass density in the range of 50-250, preferably 70-230 deniers, warp tensile strength of at least 70 Ibf / in. (1.23 x 104 N / m), preferably> 80 Ibf / in. (1.40 x 104 N / m); filling tensile strength of at least 40 Ibf / in. (7.00 x 103 N / m), preferably> 50 Ibf / in. (8.76 x 103 N / m). The weave pattern is not limited and can be plain weave, plaited weave, basket weave, satin weave and the like. The weave density should not be too high for polymer-based cloth (i.e., tight weave) such that low resin impregnation and incomplete impregnation of the threads would result.
    [0017] Figure 3 is a scanning electron microscope (SEM) image of an exemplary polyester cloth that can be used for the resin-rich shell layer. This specific cloth has a weight of 110 gsm and yarn with a linear mass density of 125 deniers. As can be seen from figure 3, this type of polyester cloth is not tightly woven and contains tiny openings in the weave. When the shell layer containing this type of polyester cloth is detached from the composite surface, a resin film with a rough surface and no broken fibers is produced. Such a rough surface is desirable for bonding. Tightly woven cloths such as glass cloths can also be used to form the resin-rich shell layer to create a desirable surface roughness for composite bonding. Figure 4 shows an exemplary glass cloth that can be used for the resin-rich shell layer. This glass cloth is more tightly woven and thicker than the polyester cloth shown in figure 3; it has a weight of 205 gsm and a thickness of 175 pm.
    [0018] The resin matrix of the shell layer is formed of a curable resin composition that includes: at least one epoxidized novolac resin having epoxy functionality of at least 2; difunctional epoxy resin selected from diglycidyl ethers of polyhydric phenols; trifunctional epoxy resin selected from triglyceride ethers of aminophenols; inorganic filler particles (eg, colloidal silica); and a healing agent. The epoxidized novolac resin is composed of at least 40% by weight based on the total weight of the composition, preferably 50-70% by weight. The difunctional epoxy resin is present in an amount of 10-35%, preferably 15-25% by weight, the trifunctional epoxy resin is present in an amount of 10-30%, preferably 10-20% by weight, based on weight total resin composition.
    [0019] Examples of epoxy novolac resins include those obtained by reacting phenols such as phenol, o-cresol, m-cresol, p-cresol, p-tert-butylphenol, p-nonyl phenol, 2,6-xylenol, resorcinol, bisphenol -A, α and β-naphthol, and naphthalenediol with aldehydes such as acetaldehyde, formaldehyde, furfural, glyoxal and p-hydroxy benzaldehyde in the presence of an acid catalyst.
    [0020] Suitable epoxidized novolac resins include epoxy phenol novolac resins and cresol epoxy novolac resins represented by the following structure I:
    (I) where n is an integer from 0 to 8, R = H or CH3. When R = H, the resin is a novolac phenol resin. When R = CH3, the resin is a novolac cresol resin. Novolac epoxy phenol resins are commercially available as DEN 428, DEN 431, DEN 438, DEN 439, and DEN 485 from Dow Chemical Co. Novolac cresol epoxy resins are commercially available as ECN 1235, ECN 1273, and ECN 1299 from Ciba- Geigy Corp.
    [0021] Another suitable epoxidized novolac resin is hydrocarbon epoxy novolac resin having a dicyclopentadiene backbone represented by the following Structure II:
    where n is an integer from 0 to 7. Commercial examples of such novolac hydrocarbon epoxy resins include Tactix® 71756, Tactix® 556, and Tactix® 756 from Vantico Inc. In one embodiment, the novolac resin of Structure I is used in combination with novolac resin containing structure II dicyclopentadiene.
    [0022] Suitable difunctional epoxy resins include diglycidyl ethers of bisphenol A or bisphenol F, for example, Epon ™ 828 (liquid epoxy resin), D.E.R. 331, D.E.R. 661 (solid epoxy resin) supplied by Dow Chemical Co.
    [0023] Aminophenol triglycidyl ethers are commercially available as Araldite® MY 0510, MY 0500, MY 0600, MY 0610 from Huntsman Advanced Materials.
    [0024] Suitable curing agents for the epoxy resin in the shell layer resin composition include a class of curing agents known as Lewis Acid; trifluorboretum (BF3), boron trichloride (BCI3) and complexes thereof, such as BF3-Amine complexes and BCls-Amine complexes. Examples of BF3-Amine complexes include BF3-MEA from Ato-Tech, Anchor 1040 (BF3 complexed with benzyl amine and isopropyl amine) from Air Products, Anchor 1115 (BF3 complexed with isopropyl amine adduct) from Air Products, and Anchor 1170 (BF3 complexed with chlorobezenyl amine) also from Air Products. Examples of BCh-Amine complexes include Omincure ™ BC-120. The complexes are made to provide liquid or solid forms under conditions of normal use. Many commercially available epoxy-based prepregs include amine-based curing agents such as 3,3'-diaminodiphenyl sulfone (DDS) and dicyandiamide (DICY), which show substantially slower curing kinetics than those of a layered resin formulation. bark containing the top curing agents, for example, liquid BF3. As a result, the shell layer resin formulation can cure fast enough to minimize intermixing with the prepreg resin during the curing process together.
    [0025] Inorganic filler materials in particle form (for example, powder) are added to the shell layer resin composition as a rheology modifying component to control the flow of the resin composition and prevent agglomeration therein. Suitable inorganic fillers that can be used in the surface film composition include colloidal silica, talc, mica, calcium carbonate, alumina. The amount of inorganic filler material can be in the range of 1-10% by weight, preferably 1-5% by weight, based on the total weight of the surface film composition.
    [0026] In one embodiment, the peel layer resin composition may include, in weight percentages based on the total weight of the resin composition: approximately 45-55% phenol novolac epoxy resin; approximately 5-15% novolac epoxy resin containing dicyclopentadiene, approximately 20-30% bisphenol A diglycidyl ether; approximately 15-25% aminophenol triglycidyl ether; approximately 5-15% BF3 curing agent and approximately 1-5% inorganic filler.
    [0027] In addition, one or more organic solvents can also be added to the resin composition described above, as needed, to facilitate mixing of the components. Examples of such solvents may include, but are not limited to, methyl ethyl ketone (MEK), acetone, dimethyl acetamide and N-methyl pyrrolidone.
    [0028] The resin-rich bark layer can be formed by coating the resin composition described above on the woven cloth in order to fully impregnate the threads in the cloth using conventional heat or solvent melting coating processes. The wet peel layer is then allowed to dry if necessary to reduce the volatile content, preferably to less than 2% by weight, drying can be done by air drying at room temperature overnight followed by drying in a 140 ° oven. ° F - 170 ° F, or by drying in a high temperature oven, as necessary, to reduce the drying time. Subsequently, the dry resin-rich peel layer can be protected by applying removable release papers or synthetic films (for example, polyester films) on opposite sides. Such release papers or synthetic films must be removed before using the peel layer for surface bonding. The dry peel layer is applied to a surface of a composite substrate based on uncured (or partially cured) resin, for example, epoxy-based prepreg. Then, the shell layer together with the composite substrate is cured together. The peel layer is then removed to leave a thin resin film on the composite substrate, thereby forming a modified surface ready for bonding the adhesive with another composite substrate.
    [0029] For joint bonding and secondary bonding of two composite substrates, a curable adhesive film is applied to at least one of the modified surface of a first composite substrate that is already cured and a surface of a second composite substrate. The modified surface of the first cured composite substrate is brought into contact with a surface of the second composite substrate in such a way that the adhesive is between the substrates. Curing is then carried out to form a bonded composite structure. The terms "cure" and "cure" as used here refer to the polymerization and / or crosslinking process that can be carried out by heating, exposure to ultraviolet light or radiation.
    [0030] The joint curing of the resin-rich shell layer and the resin-based composite substrate (eg, epoxy-based prepreg) can be carried out at temperatures greater than 230 ° F (110 ° C), more specifically , within the range of 250 ° F - 375 ° F (121 ° C - 190 ° C). It has been found that an advantage of the resin-rich shell layer described here is that the shell layer can be cured in conjunction with most commercially available prepregs within the above curing range. Such prepregs include commercially available resin-impregnated cloths and / or tapes such as CYCOM 997, CYCOM 977-2, CYCOM 934, CYCOM 970, CYCOM 5317-3, CYCOM 5320-1 and CYCOM 851 from Cytec Industries Inc .; Hexply 8552 from Hexcel Corp .; and Toray 3900-2 from Toray Industries Inc. After curing together, the resin-rich shell layer has a glass transition temperature (Tg)> 140 ° C, in some embodiments, 140 ° C -200 ° C, as measured by Modulated Differential Scanning Calorimetry (DSC) method. EXAMPLES
    [0031] The following examples are illustrative of some modalities of the resin-rich shell layer disclosed here and its application, and should not be construed as limiting the scope of the present disclosure. Example 1
    [0032] A layer of resin-rich bark was prepared by impregnating a polyester cloth with a resin formulation comprised, in weight percentage: 45% phenol-formaldehyde novolac epoxy resin; 11% novolac epoxy resin containing dicyclopentadiene; 23% bisphenol A diglycidyl ether; 14% aminophenol triglycidyl ether; 5% liquid BF3 and 2% colloidal silica. The polyester cloth had the following properties: Cloth Plain weave, polyester fibers Weight 85 g / m2 Linear mass density warp 150 denier; 150 denier fill Warp tensile strength 155 Ibf / in (2.7 x 104 N / m); filling 120 Ibf / in (2.1 x 104N / m) Thickness ~ 0.005 in
    [0033] The resin formulation was mixed using a heat melting process followed by a solvent addition process. After a heat melt mixture was made, methyl ethyl ketone solvent (MEK) was added to the resin composition to form an 82% solid suspension. The wet resin composition was coated on a cloth using a solvent coating process and allowed to dry overnight at room temperature followed by a drying process on a stove to reduce the volatile content to less than 2%. The dry shell layer had a resin content of approximately 43% by weight and a thickness of approximately 140 µm.
    [0034] Alternatively, the resin formulation can also be mixed with MEK in a solvent-assisted process at room temperature. The wet resin mixture obtained at 82% solid content can be coated on the cloth in the same manner as described above.
    [0035] The dry shell layer as discussed above was used to prepare the surface of a fiber-reinforced epoxy prepreg, CYCOM 997 tape (from Cytec Industries Inc.). after curing together at 177 ° C, the shell layer was detached leaving behind a modified surface ready for bonding. A Drum Detachment test (ASTM D1781) was performed to evaluate the Peel Resistance of the shell layer. The test result indicated 11.1 Newton (2.5 in-lb / inch in width). This shows that the shell layer was easily detached. Surface analysis by ATR-FTIR (Total attenuated reflection) was performed to study the prepreg treated surface after curing and removing the shell layer. It was found that a thin layer of approximately 3-10 pm of shell layer resin was left on top of the prepreg. Figure 5 is a scanning electron microscope (SEM) image of the treated surface after the resin-rich peel layer is removed, showing that no fiber breaks from the cloth remains. Example 2
    [0036] A layer of resin-rich bark was manufactured by impregnating a polyester cloth with a resin formulation comprised, in percentage by weight: 45% of novolac phenol-formaldehyde epoxy resin; 11% novolac epoxy resin containing dicyclopentadiene; 22.5% bisphenol A diglycidyl ether; 13.5% aminophenol triglycidyl ether; 6% BF3-MEA; and 2% colloidal silica. The polyester cloth had the following properties: Cloth Smooth weave, twisted, polyester fibers Weight 110 g / m2 Linear mass density warp 126 denier; filling 126 denier Tensile strength warp 105 Ibf / in. (1.8 x 104 N / m); filling 105 Ibf / in. (1.8 x 104N / m) Thickness ~ 0.0045 in.
    [0037] The resin formulation was mixed, coated over the cloth, dried and tested in the same way as in Example 1. Similar result was seen - a thin layer of approximately 3-10 pm shell layer resin was left on top of the prepreg after the resin-rich peel layer is removed, but no broken fibers from the cloth remain. Example 3
    [0038] A layer of resin-rich bark was prepared by impregnating a polyester cloth with a resin formulation comprising, in% by weight: 44.5% novolac phenol-formaldehyde epoxy resin; 9% novolac epoxy resin containing dicyclopentadiene; 22% bisphenol A diglycidyl ether; 18% aminophenol triglycidyl ether 4.7% liquid BF3 and 1.8% colloidal silica. The polyester cloth had the following properties: Cloth Plain weave, polyester fibers Weight 85 g / m2 Linear mass density warp 150 denier; filler 150 denier Tensile strength warp 155 Ibf / in. (2.7 x 104 N / m); filling 120 Ibf / in. (2.1 x 104N / m) Thickness ~ 0.005 in.
    [0039] The resin formulation was mixed, coated over the cloth, dried and tested in the same way as in Example 1. Similar result was seen - a thin layer of approximately 3-10 pm shell layer resin was left on top of the prepreg after the resin-rich peel layer is removed, but no broken fibers from the cloth remain. Example 4
    [0040] A layer of resin-rich bark was prepared by impregnating a polyester cloth with a resin formulation comprising, in weight%: 44% phenol-formaldehyde novolac epoxy resin; 9% novolac epoxy resin containing dicyclopentadiene; 22% bisphenol A diglycidyl ether; 17% aminophenol triglycidyl ether; 6% BFa-MEA and 2% colloidal silica. The polyester cloth had the following properties: Cloth Smooth weave, twisted, polyester fibers Weight 110g / m2 Linear mass density warp 126 denier; filling 126 denier Tensile strength warp 105 Ibf / in. (1.8 x 104 N / m); filling 105 Ibf / in. (1.8 x 104N / m) Thickness ~ 0.0045 in.
    [0041] The resin formulation was mixed, coated on the cloth, dried and tested in the same way as in Example 1. Similar result was seen - a thin layer of approximately 3-10 pm shell layer resin was left on top of the prepreg after the resin-rich peel layer is removed, but no broken fibers from the cloth remain. Example 5
    [0042] A layer of resin-rich bark was prepared by impregnating a polyester cloth with a resin formulation comprised, in% by weight: 45.5% of phenol-formaldehyde novolac epoxy resin; 11.4% novolac epoxy resin containing dicyclopentadiene; 22.8% bisphenol A diglycidyl ether; 13.7% aminophenol triglycidyl ether; 4.8% liquid BF3 and 1.8% colloidal silica. The polyester cloth had the following properties: Cloth Smooth weave, twisted, polyester fibers Weight 110 g / m2 Linear mass density warp 126 denier; 126 denier filling Warp tensile strength 105 Ibf / in. (1.8 x 104 N / m); filling 105 Ibf / in. (1.8 x 104N / m) Thickness ~ 0.0045 in.
    [0043] The resin formulation was mixed, coated on the cloth, dried and tested in the same way as in Example 1. Similar result was seen - a thin layer of approximately 3-10 pm shell layer resin was left on top of the prepreg after the resin-rich peel layer is removed, but no broken fibers from the cloth remain. Example 6
    [0044] A layer of resin-rich bark was prepared by impregnating a glass cloth with a resin formulation comprising, by weight: 44.5% novolac phenol-formaldehyde epoxy resin; 8.9% novolac epoxy resin containing dicyclopentadiene; 22.3% bisphenol A diglycidyl ether; 17.8% aminophenol triglycidyl ether; 4.7% liquid BF3 and 1.8% colloidal silica. The glass cloth had the following properties: Cloth Smooth weave, glass fibers Weight 207 g / m2 Warp resistance 350 Ibf / in. (6.1 x 104 N / m); filling 260 Ibf / in. (4.6 x 104 N / m) Thickness ~ 0.007 in.
    [0045] The resin formulation was mixed, coated on the cloth in the same manner as in Example 1. After drying, the dry shell layer had a resin content of approximately 28% by weight and a thickness of approximately 195 pm. the resin-rich shell layer was then tested in the same manner as in Example 1. Similar result was seen - a thin layer of approximately 3-10 pm shell layer resin was left on top of the prepreg after the rich shell layer in resin be removed, but no broken fiber remains. Example 7
    [0046] A layer of resin-rich bark was prepared by impregnating a polyester cloth with the resin formulation disclosed in Example 6. The polyester cloth had the following properties: Cloth Smooth weave, twisted, polyester fibers Weight 110 g / m2 Linear mass density warp 126 denier; 126 denier filling Warp tensile strength 105 Ibf / in. (1.8 x 104 N / m); filling 105 Ibf / in. (1.8 x 104 N / m) Thickness ~ 0.0045 in.
    [0047] The resin formulation was mixed, coated over the cloth, dried and tested in the same way as in Example 1. Similar result was seen - a thin layer of approximately 3-10 pm shell layer resin was left on top of the prepreg after the resin-rich peel layer is removed, but no broken fibers from the cloth remain. Example 8 Double overlap shear test
    [0048] CYCOM 970 prepregs (from Cytec Industries Inc.) were bonded together using a commercially available FM 318M.05 psf adhesive (from Cytec Industries Inc.). Three to four samples of bound prepreg were tested at each test temperature. Before bonding, the bonding surface of the prepregs was prepared using the resin-rich shell layer as discussed in Example 1. Table 2 shows the average shear data at test temperatures of 23 ° C, -55 ° C and 72 ° C based on double overlap shear test (ASTM D3528). As seen in Table 2, the shell layer promotes cohesive failure at the various test temperatures. TABLE 2
    Example 9 Double cantilever beam test
    [0049] Bound prepreg samples were formed using various commercially available prepreg materials and a commercially available FM 309-l adhesive (from Cytec Industries Inc.). prior to bonding, the bonding surface of the prepregs was prepared using the resin-rich shell layer as discussed in Example 1. Double cantilever beam test (ASTM D5528) was performed at 23 ° C and -55 ° C to measure toughness of inter laminar fracture (Gic) of the connected prepregs and the results are shown in figure 6.
    [0050] CYCOM 5317-6 prepregs (from Cytec Industries Inc.) were bonded together using structural adhesive FM 309-1 M.05 psf. Before the coalition, a layer of resin-rich bark formed with the glass cloth shown in figure 4 was used to prepare the bonding surface on one of the prepregs. Figures 7A and 7B show the cohesive failure condition after Gic test of the prepregs linked together.
    [0051] The terms "first", "second" and the like do not indicate any order, quantity or importance here, but instead they are used to distinguish one element from the other, and the terms "one" and "one" here do not indicate a quantity limitation, but instead indicate the presence of at least one of the referenced item. The “approximately” or “about” modifier used with respect to a quantity is inclusive of the mentioned value and has the meaning determined by the context, (for example, includes the degree of error associated with the measurement of the specific quantity). The suffix “(s)” as used here is intended to include both the singular and the plural of the term it modifies, thereby including one or more of that term (for example, the metal (s) includes (s) one or more metals). Bands disclosed here are inclusive and independently combinable (for example, ranges of "approximately 25% by weight, or more specifically, approximately 5% by weight to approximately 20% by weight", are inclusive of the end points and all intermediate values of the ranges “approximately 5% by weight to approximately 25% by weight”, etc.).
    [0052] Although several modalities are described here, it will be recognized from the specification that various combinations of elements, variations or improvements in them can be made by those skilled in the art, and are included in the scope of the invention. In addition, many modifications can be made to adapt a specific situation or material to the teachings of the invention without departing from its essential scope. Therefore, it is intended that the invention is not limited to the specific modality disclosed as the best mode considered for carrying out the present invention, but that the invention includes all modalities included in the scope of the appended claims.
    权利要求:
    Claims (15)
    [0001]
    1. Shell layer system for surface preparation of various composite substrates, said system characterized by the fact that it comprises (a) a composite substrate (10) comprising reinforcement fibers impregnated with a first cured resin matrix; and (b) a resin-rich peel layer (11), removable adhered to a surface of the composite substrate (10), said peel layer comprising a woven cloth (11a) impregnated with a second resin matrix (11b) , cured differently from the first resin matrix, so that after manual removal of the peel layer from the surface of the composite substrate, a thin film of the second resin matrix (12) remains on the surface of the composite substrate to provide a bondable surface capable of bonding together and secondary bonding with another composite substrate, wherein the second resin matrix (11b) is formed of a resin composition comprising: at least one epoxidized novolac resin having epoxy functionality of at least 2; difunctional epoxy resin selected from diglycidyl ethers of polyhydric phenols; trifunctional epoxy resin selected from triglycidyl ethers of amino phenols; a curing agent; and inorganic filler particles; wherein the shell layer (11) has a resin content of at least 20% by weight based on the total weight of the shell layer, and wherein said woven cloth (11a) comprises a plurality of yarns woven in a pattern of weaving, said yarns having a warp tensile strength of> 70 Ibf / in. (1.23 x 104 N / m), tensile strength of filling> 40 Ibf / in. (7.00 x 103 N / m), linear warp mass density within the range of 50-250 deniers, and linear fill mass density within the range of 50-250 deniers.
    [0002]
    2. System according to claim 1, characterized by the fact that said threads have a warp tensile strength of> 80 Ibf / in. (1.40 x 104 N / m), filling tensile strength> 50 Ibf / in. (8.76 x 103 N / m), linear warp mass density within the range of 70-230 deniers, and linear fill mass density within the range of 70-230 deniers.
    [0003]
    3. System according to claim 1 or 2, characterized by the fact that the remaining thin film of the second resin matrix (12) has a thickness of 2% to 15% of the original thickness of the peel layer (11) before removal.
    [0004]
    System according to any one of claims 1-3, characterized in that the resin composition comprises at least one epoxidized novolac resin selected from epoxy phenol novolac resins and cresol epoxy novolac resins represented by the following structure:
    [0005]
    System according to any one of claims 1-4, characterized in that the resin composition further comprises a novolac epoxy resin containing dicyclopentadiene represented by the following structure:
    [0006]
    6. System according to any one of claims 1-5, characterized in that the woven cloth (11a) has a cloth weight within the range of 50 to 250 gsm or 70 to 220 gsm.
    [0007]
    System according to any one of claims 1-6, characterized in that the woven cloth (11a) has a cloth thickness within the range of 50 to 250 pm or 100 to 200 pm.
    [0008]
    8. System according to any one of claims 1-7, characterized by the fact that the threads of the woven cloth (11a) are made of materials selected from the group consisting of: polyesters, polyethylene, polypropylene, nylon, elastomeric materials, polyamides, polyimides, polyethylene imine (PEI), polyoxazole, polybenzimidazole (PBI), polyether ether ketone (PEEK) and glass.
    [0009]
    System according to any one of claims 1-8, characterized in that said layer of bark has a resin content within the range of 20% to 50% by weight based on the total weight of the layer of bark .
    [0010]
    10. The system according to any one of claims 1-9, characterized in that said peel layer has a glass transition temperature (Tg) within the range of 140 ° C to 200 ° C.
    [0011]
    11. System according to any one of claims 1-10, characterized by the fact that the curing agent is selected from the group consisting of BF3, BCI3 and complexes thereof.
    [0012]
    System according to any one of claims 1-11, characterized by the fact that said second resin matrix (11b) is formed of a resin composition comprising: novolac epoxy phenol resin having epoxy functionality of at least 2 ; novolac epoxy resin containing dicyclopentadiene having epoxy functionality of at least 2; bisphenol A diglycidyl ether; aminophenol triglycidyl ether; a curing agent selected from the group consisting of BF3, BCI3 and complexes thereof; and smoked silica.
    [0013]
    13. The system according to any one of claims 1-12, characterized by the fact that novolac resins make up at least 20% by weight based on the total weight of the composition.
    [0014]
    14. Method for surface preparation of various composite substrates using the system as defined in claim 1, characterized by the fact that it comprises: (a) providing a composite substrate (10) comprising reinforcement fibers impregnated with a first resin matrix ; (b) placing a resin-rich shell layer (11) in contact with a surface of the composite substrate (10), said shell layer being formed by impregnating a woven cloth (11a) with a curable resin composition (11b ) different from the resin matrix of the composite substrate and comprising: at least one epoxidized novolac resin having epoxy functionality of at least 2; difunctional epoxy resin selected from diglycidyl ethers of polyhydric phenols; trifunctional epoxy resin selected from triglycidyl ethers of aminophenols; a curing agent; and inorganic filler particles, wherein the woven cloth (11a) comprises a plurality of yarns woven in a weave pattern, the yarns having a warp tensile strength> 70 Ibf / in. (1.23 x 104 N / m), tensile strength of filling> 40 Ibf / in. (7.00 x 103 N / m), density of linear warp mass within the range of 50-250 deniers, and density of linear filler mass within the range of 50-250 deniers and said layer of bark (11) has a resin content of at least 20% by weight based on the total weight of the shell layer; (c) curing the shell layer and the composite substrate (10) together; and (d) removing the peel layer from the surface of the composite substrate (10) such that a thin resin film from the peel layer remains on the surface of the composite substrate to provide a bondable surface capable of bonding together. and secondary bonding with another composite substrate; wherein said curing together is carried out at a temperature greater than 230 ° F (110 ° C) or 250 ° F to 375 ° F (121 ° C to 190 ° C).
    [0015]
    15. Method of forming a bonded composite structure, characterized by the fact that it comprises the method for surface preparation of various composite substrates as defined in claim 14 wherein the curing together in step (c) is at a temperature greater than 230 ° F (110 ° C); and wherein after removing the shell layer in step (d), no fibrous material of the woven cloth (11a) remains on the same surface; and further comprises the steps of: (e) providing a second composite substrate comprising reinforcement fibers impregnated with a second resin matrix; (f) applying an adhesive film to the bondable surface of the first substrate or a surface of the second substrate; (g) placing the bondable surface of the first composite substrate (10) in contact with a surface of the second composite substrate with the adhesive film between them; and (h) curing to bond the first and second substrates.
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    同族专利:
    公开号 | 公开日
    AU2012362983B2|2016-11-10|
    AU2016256666B2|2018-01-18|
    TW201345716A|2013-11-16|
    AU2012362983A1|2014-04-17|
    EP2797733B1|2016-11-16|
    US20130129957A1|2013-05-23|
    JP6275796B2|2018-02-07|
    JP2017101219A|2017-06-08|
    ES2616241T3|2017-06-12|
    EP2797733A1|2014-11-05|
    TWI597166B|2017-09-01|
    BR112014012123B8|2020-09-01|
    CA2862191A1|2013-07-04|
    MY173766A|2020-02-19|
    WO2013101354A1|2013-07-04|
    KR101972314B1|2019-04-25|
    BR112014012123A2|2017-06-13|
    CA2862191C|2019-03-12|
    US20170066226A1|2017-03-09|
    EP3141379A1|2017-03-15|
    US10093081B2|2018-10-09|
    RU2602102C2|2016-11-10|
    BR112014012123A8|2017-06-20|
    MX345546B|2017-02-03|
    MX2014006215A|2014-08-08|
    CN103946012A|2014-07-23|
    IN2014CN04740A|2015-09-18|
    JP2015508346A|2015-03-19|
    ES2693221T3|2018-12-10|
    RU2014131471A|2016-02-20|
    KR20140107333A|2014-09-04|
    JP6033328B2|2016-11-30|
    EP3141379B1|2018-08-01|
    US9473459B2|2016-10-18|
    RU2646218C1|2018-03-02|
    AU2016256666A1|2016-11-24|
    CN103946012B|2016-01-20|
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    法律状态:
    2018-03-27| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2019-10-08| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2020-03-31| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|
    2020-07-21| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2020-08-11| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 16/11/2012, OBSERVADAS AS CONDICOES LEGAIS. |
    2020-09-01| B16C| Correction of notification of the grant [chapter 16.3 patent gazette]|Free format text: REF. RPI 2588 DE 11/08/2020 QUANTO AO ENDERECO. |
    优先权:
    申请号 | 申请日 | 专利标题
    US201161582096P| true| 2011-12-30|2011-12-30|
    US61/582096|2011-12-30|
    PCT/US2012/065389|WO2013101354A1|2011-12-30|2012-11-16|Peel ply, method of surface preparation and bonding composite structures using the same|
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