WO2013146900A1 - 接合部材の製造方法及び接合部材 - Google Patents
接合部材の製造方法及び接合部材 Download PDFInfo
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- WO2013146900A1 WO2013146900A1 PCT/JP2013/059039 JP2013059039W WO2013146900A1 WO 2013146900 A1 WO2013146900 A1 WO 2013146900A1 JP 2013059039 W JP2013059039 W JP 2013059039W WO 2013146900 A1 WO2013146900 A1 WO 2013146900A1
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- WIPO (PCT)
- Prior art keywords
- carbon fiber
- composite material
- thermoplastic resin
- metal
- fiber composite
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- Y10T428/24545—Containing metal or metal compound
Definitions
- the present invention relates to a method for producing a joining member of a thermoplastic carbon fiber composite material and a metal, and a joining member obtained by the method.
- thermosetting carbon fiber composite materials have high specific strength and specific rigidity and are lightweight, they are used in various directions as extremely excellent materials.
- thermosetting carbon fiber composite material using a thermosetting resin as a matrix to dissimilar materials, especially metals, joining and adhesives using bolts, nuts, rivets, etc., which are mechanical joining Bonding using is used.
- Mechanical joining with bolts, nuts, etc. generally increases weight.
- it is generally necessary to secure an adhesive layer having a certain thickness in order to ensure strength, and a considerable amount of adhesive is required particularly when joining a large member.
- thermoplastic carbon fiber composite material is a material within a range in which the thermoplastic resin is compatible. They are joined together by welding, and joint strength similar to that of a joined body of matrix resins can be expected.
- thermoplastic carbon fiber composite material is often difficult to join with a metal by welding (fusion) of a matrix resin.
- Patent Document 1 describes that a metal and a resin are joined by welding. Specifically, it is described that both can be joined by an anchor effect by injection molding a resin on an aluminum material having a fine porous surface.
- Patent Documents 2 to 6 describe that a metal surface is treated to bond a resin and a metal.
- Patent Document 7 describes a method of arranging and bonding an intermediate resin layer having an affinity for both a metal and the composite material. ing.
- Japanese Unexamined Patent Publication No. 2003-103563 Japanese Patent Publication No. 5-51671 International Publication No. 2009/157445 International Publication No. 2007/0772603 Japanese Unexamined Patent Publication No. 2011-235570 International Publication No. 2012/074083 Japanese Unexamined Patent Publication No. 2006-297927
- thermoplastic carbon fiber composite material using the thermoplastic resin as a matrix is that the shape can be easily changed by applying heat. Therefore, injection or press molding can be performed in a very short time as compared with a thermosetting carbon fiber composite material using a thermosetting resin as a matrix. Therefore, in the thermoplastic resin carbon fiber composite material, if the thermoplastic resin of the matrix can be used for joining, the carbon fiber composite material and the metal are extremely simple and extremely efficient by thermocompression bonding in a mold. It is considered that the joining member can be molded at once as well as.
- thermoplastic resin of the matrix is in a state of “seeding” into the carbon fiber bundle in the thermoplastic carbon fiber composite material. Therefore, the thermoplastic resin does not necessarily exist homogeneously on the surface, and because there is a “deficient” portion of the thermoplastic resin, sufficient bonding strength does not appear or the bonding strength varies greatly. There are concerns. In addition, since carbon fibers cause so-called electric corrosion with respect to metals, carbon fibers directly corrode the metals in portions where the matrix resin is deficient, causing corrosion of the metals.
- the main object of the present invention is to provide a method for manufacturing a joining member in which a thermoplastic carbon fiber composite material and a metal are firmly joined.
- the present inventors formed an uneven shape having a specific depth on the metal surface portion to be bonded to the composite material, A thermoplastic resin layer having a specific thickness is provided between the metal surface portion and the composite material, and the joining portion including the thermoplastic resin layer is heated to form heat that constitutes the thermoplastic resin layer and the thermoplastic composite material.
- the present inventors have found that the metal and the composite material can be firmly and stably adhered and bonded by melting a part of the plastic resin so that the metal and the composite material are closely bonded and bonded.
- the present invention A method for producing a joining member obtained by joining a carbon fiber composite material having a thermoplastic resin matrix and a metal, Forming a concavo-convex shape having a depth of 0.02 to 0.6 mm on the metal surface of the joint portion; and Providing a thermoplastic resin layer having a thickness in the range of 5 ⁇ m or more and 5 mm or less at the joint between the metal and the composite material (ii); And a step (iii) of firmly joining the metal and the carbon fiber composite material by heating the joining portion to melt the thermoplastic resin layer.
- thermoplastic carbon fiber composite material and a metal can be joined firmly and stably by a simple method. Furthermore, since the carbon fiber composite material and the metal are bonded via the thermoplastic resin, it is possible to simultaneously prevent electrolytic corrosion caused by the carbon fibers. And the joining member of a carbon fiber composite material and a metal can be obtained easily and in a short time. Moreover, since joining and shaping
- the present invention is a method for producing a joining member formed by joining a carbon fiber composite material (thermoplastic carbon fiber composite material) having a thermoplastic resin as a matrix and a metal, Forming a concavo-convex shape having a depth of 0.02 to 0.6 mm on the metal surface of the joint portion; and Providing a thermoplastic resin layer having a thickness in the range of 5 ⁇ m or more and 5 mm or less at a joint between the metal and the carbon fiber composite material (ii); (Iii) a step of strongly bonding the metal and the thermoplastic carbon fiber composite material by heating the bonding portion to melt the thermoplastic resin layer; Is included.
- the thermoplastic carbon fiber composite material used for joining with a metal in the present invention is a composite material containing a thermoplastic resin as a matrix and carbon fibers as reinforcing fibers in the matrix.
- the thermoplastic carbon fiber composite material preferably contains 50 to 1000 parts by weight of a thermoplastic resin with respect to 100 parts by weight of the carbon fiber. More preferably, the thermoplastic resin is 50 to 400 parts by weight with respect to 100 parts by weight of the carbon fiber, and still more preferably 50 to 100 parts by weight with respect to 100 parts by weight of the carbon fiber. If the thermoplastic resin is 50 parts by weight or more with respect to 100 parts by weight of the carbon fibers, it is preferable because dry carbon fibers exposed from the matrix resin hardly increase. In addition, if the thermoplastic resin is 1000 parts by weight or less with respect to 100 parts by weight of the carbon fiber, the carbon fiber is contained in an appropriate amount, which is suitable as a structural material.
- thermoplastic resin examples include polyamide, polycarbonate, polyoxymethylene, polyphenylene sulfide, polyphenylene ether, modified polyphenylene ether, polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polyethylene, polypropylene, polystyrene, polymethyl methacrylate, AS resin. , ABS resin.
- at least one selected from the group consisting of polyamide, polypropylene, polycarbonate, and polyphenylene sulfide is preferable from the viewpoint of cost and physical properties.
- PA polyamide
- PA6 also referred to as polycaproamide or polycaprolactam
- PA26 polyethylene adipamide
- PA46 polytetramethylene adipamide
- PA66 polyhexamethylene adipamide
- PA69 polyhexamethylene azepamide
- PA610 polyhexamethylene sebacamide
- PA611 polyhexamethylene undecanamide
- PA612 polyhexamethylene dodecanamide
- PA11 polyundecaneamide
- PA12 polydodecanamide
- PA12 polydodecanethylenedodecanamide
- PA6T polyhexamethylene terephthalamide
- PA6I Poly Oxamethylene isophthalamide
- PA912 polynonamethylene dodecamide
- PA1012 polydecanamethylene dode
- the form of the carbon fiber in the thermoplastic carbon fiber composite material is not particularly limited, and may be a discontinuous fiber or a continuous fiber.
- continuous fibers it may be a woven fabric or a sheet formed by arranging fibers in one direction, for example, a so-called UD sheet in which strands of continuous fibers are laminated.
- the fibers can be laminated in multiple layers by changing the fiber arrangement direction of each layer, for example, alternately in the orthogonal direction. Further, the laminated surfaces may be arranged symmetrically in the thickness direction.
- the carbon fiber may exist in a fiber bundle state in the composite material, or a fiber bundle and a single yarn state may be mixed. Substantially only single yarns may be present dispersed.
- a sheet made of such carbon fibers may be used, or a random mat arranged so as to be randomly dispersed and overlapped in the plane may be used.
- the discontinuous carbon fibers are preferably a mixture of carbon fiber bundles in which a large number of single yarns are bundled together with single yarns or those close to them, and they are present at a specific ratio.
- discontinuous carbon fibers are randomly arranged in the surface of the composite material, that is, randomly two-dimensionally, when moldability or a mold is used as a sheet-like molded product This is preferable because the formability of the resin becomes good.
- the average fiber length is preferably in the range of 3 mm or more and 100 mm or less, preferably 5 mm or more from the viewpoint of ease of molding and bonding strength when producing a molded body having a desired shape.
- the thing of the range of 50 mm or less is more preferable. If the average fiber length of the carbon fiber is 3 mm or more, the heat shrinkage rate after bonding of the composite material is small, and if the average fiber length is 100 mm or less, the exposure ratio of the carbon fiber to the surface of the composite material is suppressed. Since a sufficient contact area can be ensured, a sufficient bonding strength can be obtained.
- the thermoplastic carbon fiber composite material is composed of an isotropic random mat in which discontinuous carbon fibers are randomly arranged two-dimensionally and a thermoplastic resin, and the following formula (a) in the mat is used.
- the ratio of the carbon fiber bundle (A) composed of the defined number of critical single yarns or more to the total amount of fibers of the mat is preferably 20 Vol% or more and 99 Vol% or less, more preferably 20 Vol% or more and less than 99 Vol%, and further preferably 30 Vol% or more. It is particularly preferable that it is less than 90% by volume, particularly preferably 35 to 80% by volume, and the average number of fibers (N) in the carbon fiber bundle (A) satisfies the following formula (b).
- Critical number of single yarns 600 / D (a) 0.7 ⁇ 10 4 / D 2 ⁇ N ⁇ 1 ⁇ 10 5 / D 2 (b) (Where D is the average fiber diameter ( ⁇ m) of the carbon fiber)
- a random mat constituting such a thermoplastic carbon fiber composite material can be produced, for example, according to a method described in International Publication No. 2012/105080, Japanese Patent Application Laid-Open No. 2013-49208, and the like.
- strands made of a plurality of carbon fibers are continuously slit along the fiber length direction as necessary to form a plurality of narrow strands having a width of 0.05 to 5 mm, and then continuous to an average fiber length of 3 to 100 mm. Cut it.
- an isotropic random mat mat can be obtained by depositing the cut chopped strands (carbon fiber bundles) in layers on a breathable conveyor net or the like in a state where the gas is blown and opened.
- thermoplastic resin is deposited together with carbon fibers on a breathable net conveyor in a mat form, or a thermoplastic resin melted in the mat carbon fiber layer is supplied in a film form.
- a method for producing a two-dimensional isotropic random mat including a thermoplastic resin by permeation can also be employed.
- the “two-dimensional isotropic random mat” refers to a homogeneous mat in which discontinuous carbon fibers are arranged in a random direction in a horizontal plane and has no directionality in the plane.
- An isotropic thermoplastic carbon fiber composite material can be obtained by uniformly impregnating such a two-dimensional isotropic random mat with a thermoplastic resin.
- the carbon fiber bundle (B1) and / or the carbon fiber single yarn (B2) can be opened.
- the ratio of the carbon fiber bundle (A) in the isotropic random mat to the total amount of carbon fibers is, for example, 20 Vol% or more and less than 99 Vol%, preferably 30 Vol% or more and less than 90 Vol%, more preferably 35 to 80 Vol%, and the carbon fiber bundle What is necessary is just to set it as the isotropic random mat which the average fiber number (N) in (A) satisfy
- it is also possible to form an isotropic random mat containing carbon fibers on the nonwoven fabric by disposing a nonwoven fabric made of thermoplastic resin on the net conveyor and moving the nonwoven fabric together with the net conveyor. It is.
- thermoplastic carbon fiber composite material produced using an isotropic random mat containing a specific amount of fiber bundles in which a certain number of carbon fibers are converged has particularly good bondability with a metal member described later. is there.
- the reason has not yet been elucidated it is presumed to be caused by the difference in thermal shrinkage between the thermoplastic carbon fiber composite material and the metal, the bonding area, and the surface state of the composite material.
- thermoplastic resin any of the above-mentioned random mats, papermaking sheets containing discontinuous fibers, or UD sheets in which continuous fibers are unidirectionally arranged, are in a state of containing a thermoplastic resin, and are heated and pressed in a single layer or a plurality of layers.
- a carbon fiber composite material having a thermoplastic resin as a matrix is obtained by melting a thermoplastic resin present in the sheet and impregnating between the fibers.
- the thermoplastic resin in this case may be supplied at the time of producing the carbon fiber mat or sheet. After the production of the carbon fiber-containing mat or sheet, the thermoplastic resin is laminated or heated and pressed to laminate the layer containing the thermoplastic resin.
- the sheet may be impregnated with a thermoplastic resin.
- thermoplastic carbon fiber composite materials is not limited to a flat plate shape, and may be formed into a cross-section such as an L shape, a T shape, an H shape, a U shape, a hem shape, etc. It may have a curved surface.
- thermoplastic carbon fiber composite material for example, a long fiber pellet, that is, a pellet obtained in a process of cutting a molten resin after adjusting it to a predetermined viscosity and impregnating the carbon fiber of continuous fibers is cut.
- a method of forming into a predetermined shape by an injection molding machine may be used.
- the above pellets may be formed into a predetermined shape by an injection molding machine, and a thermoplastic resin is melted on a continuous fiber UD sheet or a wet paper sheet of discontinuous fibers.
- An impregnated composite material may be used.
- thermoplastic carbon fiber composite material used in the present invention is not limited to a composite material in which the reinforcing fiber is composed of only carbon fiber, and 50% by weight or more, preferably 70% by weight or more of the reinforcing fiber is made of carbon fiber.
- a composite material comprising That is, other reinforcing fibers such as aramid fibers and glass fibers may be used instead of carbon fibers within a range of less than 50% by weight, preferably less than 30% by weight of the reinforcing fibers contained in the composite material.
- metals such as iron, stainless steel, aluminum, copper, brass, nickel, zinc, or these alloys are mentioned.
- a metal contains at least 1 sort (s) selected from iron and aluminum, and the element which comprises a metal mainly has iron or aluminum more preferable.
- “mainly” means that the content occupies 90% by weight or more.
- SS materials general structural rolled steel materials
- SPCC materials cold rolled steel materials
- high-tensile materials high-tensile steel materials
- stainless steels such as SUS304 and 316, 1000-700 series aluminum and alloys thereof Preferably used.
- the shape of the metal member to be joined is not particularly limited, and can be appropriately selected according to the joining member to be obtained.
- these metal members may contain two or more kinds of metals, and at least the surface may be a member containing metal, and the surface may be metal-plated.
- the shape is not limited to a flat plate shape as long as a surface necessary for joining with the thermoplastic carbon fiber composite material is secured, and any shape can be used. It may be a metal member having a cross-section such as a letter shape, an H-shape, a U-shape, a square shape, or a cylindrical shape, or may have a curved surface.
- the metal to be joined has unevenness with a depth of 0.02 to 0.6 mm, preferably 0.05 to 0.5 mm, on a part or all of the surface to be joined.
- This unevenness can be formed, for example, by subjecting a metal surface to laser irradiation, blasting, polishing, cutting, file processing, or chemical treatment.
- the thermoplastic resin melted by heating enters the concave portions of the irregularities on the metal surface, and higher bonding strength is obtained. can get.
- the lattice shape with an interval of 0.02 to 0.6 mm, or the concave portion of the concavo-convex shape is a recess having a diameter of 0.02 to 0.6 mm.
- the laser beam spot diameter of the 20 W model is narrowed down to ⁇ 0.02 to 0.6 mm, the distance between the laser spot centers is 0.02 to 0.6 mm in a lattice pattern, and the depth is 0
- a groove having a U-shaped cross section or V-shaped cross section of 0.02 to 0.6 mm can be formed.
- the groove width is preferably 0.05 to 0.5 mm.
- the metal surface In the laser treatment, it is particularly preferable to irradiate the metal surface with laser light having a wavelength of 300 nm to 1,100 nm with an intensity of 50 W / mm 2 or more.
- laser light having a wavelength of 300 nm to 1,100 nm with an intensity of 50 W / mm 2 or more.
- various lasers such as solid lasers, liquid lasers, gas lasers, semiconductor lasers, and chemical lasers can be used.
- solid lasers for example, YAG (yttrium, aluminum, garnet) lasers and sapphire lasers can be used.
- the gas laser include a carbon dioxide laser and a helium neon laser.
- blasting examples include grit blasting, sand blasting, shot blasting, and wet blasting, and sand blasting is preferred.
- a blasting material with a particle size (diameter) of 40 to 2000 ⁇ m is used, and a depression that can be regarded as a sphere with a ⁇ (diameter) of 0.02 to 0.6 mm and a depth of 0.02 to 0.6 mm. Can be formed.
- the blast material metal, ceramic, dry ice or the like can be used.
- the arrangement of the irregularities formed on the metal surface to be the joining portion may be regular or irregular, but in order to obtain higher bonding strength, the total area of the irregularities is the metal surface area of the joining portion. It is preferable to arrange so that it occupies 10% or more.
- the depth, shape, size, etc. of the individual irregularities formed on the metal surface need not all be the same, and irregularities of various shapes may be mixed.
- the depth of the unevenness is the depth to the deepest part of the groove or depression measured on the basis of the flat surface when only a recess such as a groove or depression is formed on the flat metal surface.
- the depth to the deepest portion of the concave portion measured with reference to the horizontal plane including the most raised portion of the convex portion is indicated.
- 10 areas of 1 cm square are randomly selected on the metal surface on which the unevenness is formed, the above depth is measured for all the unevenness existing in each area, and the average value thereof is calculated as the depth of the unevenness. To do.
- the method for producing a joining member of the present invention may include a step (iA) of providing an organic coating layer on a metal surface on which irregularities are formed.
- the step (iA) is preferably a step of providing an organic coating layer between the metal surface on which the irregularities are formed and the thermoplastic resin layer, and is performed between the step (i) and the step (ii). preferable.
- a thin layer of an organic compound may be formed in advance on the surfaces to be joined by a method, etc., and used for joining. Adhesiveness with the thermoplastic resin layer can be further improved.
- organic coating layer a layer containing a triazine thiol derivative is preferable.
- the organic coating layer is not necessarily formed on the entire surface of the metal to be joined, and the thickness is not particularly limited as long as the adhesiveness can be secured.
- the average thickness of the organic coating layer is preferably 0.005 to 10 ⁇ m.
- Preferred examples of the triazine thiol derivative suitable for forming the organic coating layer include a dehydrated silanol-containing triazine thiol derivative or an alkoxysilane-containing triazine thiol derivative that can be expected to be chemically bonded to a metal.
- the alkoxysilane-containing triazine thiol derivative is selected from the group consisting of a compound represented by the following formula (1), a compound represented by the following formula (2), and a compound represented by the following formula (3). More than one type is preferred.
- R 1 represents H—, CH 3 —, C 2 H 5 —, CH 2 ⁇ CHCH 2 —, C 4 H 9 —, C 6 H 5 —. , C 6 H 13- .
- R 2 represents —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, —CH 2 CH 2 CH 2 CH 2 CH 2 CH 2 —, —CH 2 CH 2 SCH 2 CH 2 —, —CH 2 CH 2 NHCH 2 CH 2 CH 2 —.
- R 3 is — (CH 2 CH 2 ) 2 CHOCONHCH 2 CH 2 CH 2 — or — (CH 2 CH 2 ) 2 N—CH 2 CH 2 CH 2 —, in which case N, R 3 and Becomes a ring structure.
- X in the formula represents CH 3 —, C 2 H 5 —, nC 3 H 7 —, iC 3 H 7 —, nC 4 H 9 —, iC 4 H 9 —, t—C 4 H 9 —, C 6 H 5 —
- Y is CH 3 O—, C 2 H 5 O—, n—C 3 H 7 O—, iC 3 H 7 O -, N-C 4 H 9 O-, i-C 4 H 9 O-, t-C 4 H 9 O-, C 6 H 5 O-, where n is 1 to 3 An integer, M is —H or an alkali metal. ]
- R 4 represents —S—, —O—, —NHCH 2 C 6 H 4 O—, —NHC 6 H 4 O—, —NHC 6 H 3 (Cl) O—, —NHCH 2 C 6 H 3 (NO 2 ) O—, —NHC 6 H 3 (NO 2 ) O—, —NHC 6 H 3 (CN) O—, —NHC 6 H 2 (NO 2 ) 2 O—, —NHC 6 H 3 (COOCH 3 ) O—, —NHC 10 H 6 O—, —NHC 10 H 5 (NO 2 ) O—, —NHC 10 H 4 (NO 2 ) 2 O—, —NHC 6 H 4 S— , —NHC 6 H 3 (Cl) S—, —NHCH 2 C 6 H 3 (NO 2 ) S—, —NHC 6 H 3 (CN) S —, —NHC 6 H 2 (NO)
- the alkali metal is preferably at least one selected from the group consisting of lithium, sodium, potassium, rubidium, and cesium.
- triazine thiol derivative used in the present invention include triethoxysilylpropylaminotriazine thiol monosodium, which is an alkoxysilane-containing triazine thiol derivative exhibiting an excellent effect, and the chemical formula thereof is represented by the following formula (4). expressed.
- the triazine thiol derivative-containing layer As a method for forming the triazine thiol derivative-containing layer, a method described in International Publication No. 2009/157445 is preferably exemplified. Specifically, after the metal to be bonded is dipped in a water ethanol solution of an alkoxysilane-containing triazine thiol, it is pulled up and subjected to a heat treatment to complete and dry the reaction. Moreover, the method of heat-processing, after apply
- the triazine thiol derivative-containing layer may contain a substance other than the triazine thiol derivative as long as the object of the present invention is not impaired.
- the organic coating layer is preferably a triazine thiol derivative-containing layer as described above, but other organic compounds having the same function as this, for example, silane coupling agents, polar functional groups such as hydroxyl groups and carboxyl groups It may be a layer of a compound having a group.
- Metal compound layer It is preferable to include a metal compound layer such as a hydroxide, carboxylate, phosphate, or sulfate between the triazine thiol derivative-containing layer and the metal because further improvement in bonding strength can be expected.
- a metal compound layer such as a hydroxide, carboxylate, phosphate, or sulfate between the triazine thiol derivative-containing layer and the metal because further improvement in bonding strength can be expected.
- a method for forming the metal compound layer a method described in International Publication No. 2009/157445 is preferably mentioned. Specifically, prior to forming the triazine thiol derivative-containing layer on the surface of the metal to be bonded, hydrochloric acid is used. Examples of the method include immersing a metal in an acid such as sulfuric acid or phosphoric acid, or applying it to the surface of the metal and drying it.
- thermoplastic resin layer In the present invention, a thickness of 5 ⁇ m to 5 mm, preferably 20 ⁇ m to between a carbon fiber composite material having a thermoplastic resin matrix and a metal surface on which a concavo-convex shape having a depth of 0.02 to 0.6 mm is formed.
- the thermoplastic resin layer is preferably formed from a layer containing at least one heat-meltable film, sheet, woven fabric, non-woven fabric, or powder substantially composed of a thermoplastic resin. More preferably, it is formed from a sheet or a layer containing a nonwoven fabric.
- substantially means, in addition to the thermoplastic resin, if necessary (in a proportion of 20% by weight or less), for example, a stabilizer, a flame retardant, a pigment, a filler, a plasticizer, It means that an additive such as a melt viscosity modifier may be included.
- thermoplastic resin layer is used in the form of a film, sheet, woven fabric, non-woven fabric or powder, and is thermocompression bonded to the surface of a metal or thermoplastic carbon fiber composite material, or a molten thermoplastic resin is injection molded or melt extruded. It can arrange
- the kind of the thermoplastic resin constituting the thermoplastic resin layer is preferably a resin that is compatible with the matrix resin of the thermoplastic carbon fiber composite material described above, and is the same as the matrix resin constituting the thermoplastic carbon fiber composite material.
- a resin is preferred. It is more preferable from the viewpoint of bonding strength that the thermoplastic resin constituting the thermoplastic resin layer and the thermoplastic resin constituting the matrix resin of the thermoplastic carbon fiber composite material are the same type of resin.
- thermoplastic resin constituting the thermoplastic resin layer examples include polyamide, polycarbonate, polyoxymethylene, polyphenylene sulfide, polyphenylene ether, modified polyphenylene ether, polyethylene terephthalate, polybutylene, as in the matrix resin of the thermoplastic carbon fiber composite material.
- examples include terephthalate, polyethylene naphthalate, polyethylene, polypropylene, polystyrene, polymethyl methacrylate, AS resin, and ABS resin.
- at least one selected from the group consisting of polyamide, polypropylene, polycarbonate, and polyphenylene sulfide is preferable in terms of cost and physical properties.
- thermoplastic resin layer the same polyamide as that exemplified as the matrix resin of the thermoplastic carbon fiber composite material is particularly preferable.
- thermoplastic resins may contain additives such as stabilizers, flame retardants, pigments, fillers, plasticizers, and melt viscosity modifiers as necessary.
- the thickness of the thermoplastic resin layer is 5 ⁇ m or more and 5 mm or less, preferably 20 ⁇ m or more and 4 mm or less, and more preferably 40 ⁇ m or more and 3 mm or less. If the thickness of the thermoplastic resin layer is 5 ⁇ m or more, sufficient bonding strength can be obtained. When the thickness of the thermoplastic resin layer exceeds 5 mm, when a shearing load is applied to one or both of the metal and the carbon fiber composite material, a moment may act on the joint surface, and the strength may decrease as a whole. By providing such a thermoplastic resin layer with a thickness of 5 ⁇ m or more, sufficient resin can be supplied at the time of fusion in the step (iii), and the carbon fiber can be prevented from coming into contact with the metal. Prevention can be expected.
- the thickness of the thermoplastic resin layer refers to the thickness before melting when the thermoplastic resin layer is substantially composed of a film, a sheet, a nonwoven fabric, or the like. Refers to the total thickness.
- thermoplastic resin layer does not need to be provided on the entire metal surface to be joined and the entire surface of the composite material, and may be a part as long as adhesion can be secured.
- a thermoplastic resin layer is disposed at the joint in the form of a film, sheet, woven fabric, nonwoven fabric, and / or powder, and heat and pressure are applied to impregnate the thermoplastic carbon fiber composite material with the thermoplastic resin. It is melted to the extent possible, and finally the metal and the carbon fiber composite material are joined.
- thermoplastic resin layer A film, sheet, nonwoven fabric, or the like that becomes a thermoplastic resin layer is heated and melted in a state where it is in contact with at least one of a metal uneven surface and a composite material surface, preferably a metal uneven surface, and then solidified by cooling.
- a homogeneous thermoplastic resin layer can be formed on the surface.
- the temperature of the step of forming the thermoplastic resin layer on the surface of the metal or composite material to be joined is preferably in the range of the melting temperature of the thermoplastic resin + 15 ° C. or higher and the decomposition temperature ⁇ 30 ° C. or lower, and the melting temperature + 20 ° C. or higher. And a decomposition range of ⁇ 20 ° C. or lower is more preferable.
- thermoplastic resin when the thermoplastic resin is PA6 (melting point 220 ° C.), a preferred temperature is 235 to 300 ° C.
- the “melting temperature” is the melting point of the resin constituting the thermoplastic resin layer, and is the temperature at which sufficient fluidity is started for those having no melting point.
- the thermoplastic resin may not be familiar with the surface, and if it exceeds the above range, decomposition of the thermoplastic resin may proceed.
- the time for maintaining the temperature is preferably as short as possible if the time for essential joining of the thermoplastic carbon fiber composite material and the metal can be secured, and is preferably about 10 seconds to 10 minutes, for example.
- a molten thermoplastic resin may be directly coated on at least one of the metal uneven surface and the composite material surface to form a thermoplastic resin layer on the joint surface.
- the joint surface between the thermoplastic carbon fiber composite material and the metal is not limited to a flat surface, and may be a curved surface or an uneven surface.
- a non-woven fabric made of a flexible thermoplastic resin is interposed between both joining surfaces and melted to form a thermoplastic resin layer, there is a slight gap between the composite material to be joined and the metal surface. Even if there is a gap, it can be joined without any problem.
- a thermoplastic resin layer can also be made into the layer which consists of a nonwoven fabric substantially.
- a non-woven fabric made of a thermoplastic resin is interposed between the thermoplastic carbon fiber composite material and the surface of the metal member having a concavo-convex shape, and the thermoplastic resin constituting the non-woven fabric is melted by heating, thereby making the metal It is preferable to join the surface and the thermoplastic carbon fiber composite material.
- the nonwoven fabric used here is composed of a thermoplastic resin that melts by heating and adheres to the metal.
- thermoplastic resins for example, heat-meltable polyamide (nylon), polycarbonate, polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polyethylene, polypropylene and the like are preferable. Of these, polyamide and polypropylene are more preferable from the viewpoint of cost and physical properties. Further, as polyamide (sometimes abbreviated as PA), PA6, PA66 or a copolymer or blend containing these as a main component is particularly preferable. These nonwoven fabric-constituting resins may contain additives such as stabilizers, flame retardants, pigments, fillers and the like as necessary.
- additives such as stabilizers, flame retardants, pigments, fillers and the like as necessary.
- the constituent fiber of the nonwoven fabric may be a continuous fiber or a short fiber, but a fiber that is easily melted by heating is preferable. From this viewpoint, a fiber that has not been stretched or heat-treated is suitable.
- a nonwoven fabric containing the same kind of thermoplastic resin as the thermoplastic resin that is the matrix of the thermoplastic carbon fiber composite material is used as the nonwoven fabric, the entire resin is compatible with the matrix resin of the thermoplastic carbon fiber composite material by heating and melting described later. This is preferred because the layers are completely homogeneously integrated.
- non-woven fabrics manufactured by any of dry methods such as airlaid method and needle punch method, and wet methods such as papermaking method can be used, but it consists of continuous fibers with excellent cost, productivity and meltability.
- the use of nonwoven fabrics by the spunbond method is particularly preferred.
- the nonwoven fabric only one nonwoven fabric may be used, or a laminate of a plurality of nonwoven fabrics may be used. In the latter case, different types of non-woven fabrics can be combined and laminated.
- This non-woven fabric is preferably provided over the entire surface on which the thermoplastic carbon fiber composite material and the metal member are to be joined, but may be provided locally if the necessary bond strength (adhesiveness) can be ensured.
- the nonwoven fabric may contain an appropriate amount of moisture or a plasticizer, for the purpose of facilitating melting of the nonwoven fabric by heating, if necessary.
- the nonwoven fabric preferably has a total basis weight of 10 to 500 g / m 2 and a total bulk density of 0.01 to 0.8 g / cm 3 .
- the nonwoven fabric having the total weight and the total bulk density within the above ranges have appropriate air permeability and elasticity in the thickness direction, and therefore, the thermoplastic carbon fiber composite material and the metal member are laminated with the nonwoven fabric interposed. When heated and pressurized, it is melted under a substantially uniform pressure. For this reason, the penetration
- the nonwoven fabric has a moderate flexibility than the film, it is easy to follow the shape even when the joining surface is a curved surface. It becomes possible to improve the joint strength of a site
- the “total fabric weight” and “total bulk density” of the nonwoven fabric referred to here are the fabric weight and bulk density of the entire nonwoven fabric, respectively.
- the thermoplastic resin layer is composed of a single nonwoven fabric, The weight per unit area and the bulk density of the non-woven fabric are obtained.
- a thermoplastic resin layer is formed by laminating a plurality of non-woven fabrics, it is the sum of the basis weight and the bulk density of each laminated non-woven fabric.
- thermoplastic resin layer is melted by heating in a state where the thermoplastic resin layer is provided between the metal surface on which the unevenness is formed and the carbon fiber composite material, preferably At the same time, the whole is pressurized to join the metal and the carbon fiber composite material.
- the manufacturing method of the present invention includes the step (i) of forming a concavo-convex shape having a depth of 0.02 to 0.6 mm on the metal surface of the joint, and the joining between the metal and the carbon fiber composite material.
- the steps (i), (ii), and (iii) may be performed in order, and after the step (i), the steps (ii) and (iii) may be performed as one step. In the latter, the manufacturing process is simplified and the productivity is excellent.
- a step of forming an organic coating layer may be added after the step (i), and the steps (i), (iA), (ii), and (iii) may be performed in order.
- thermoplastic resin layer As the heating method in the above step (iii), heat transfer, radiation or the like using an external heater is preferable. Further, a method of heating the metal to be joined by electromagnetic induction, a method of heating by ultrasonic wave, laser, or the like can also be adopted, and the method of heating by electromagnetic induction determines the joining surface (A) between the metal and the thermoplastic resin layer. This is very preferable because it can be directly heated.
- the heating temperature is preferably not less than the melting temperature and not more than the decomposition temperature of the thermoplastic resin constituting the thermoplastic resin in the thermoplastic resin layer and the thermoplastic carbon fiber composite material, the melting temperature + 15 ° C. or more and the decomposition temperature ⁇ 30 ° C. It is more preferable that For example, when all the thermoplastic resins are PA6, 235 to 300 ° C. is preferable.
- the melted thermoplastic resin layer can be brought into contact with the thermoplastic carbon fiber composite material and pressed to provide a bonded body with better strength.
- the thermoplastic resin layer and the thermoplastic carbon fiber composite material are pressure-bonded in the step (iii). After joining, if necessary, the step (iv) of further pressing and pressing under heating is performed. Can be done.
- the pressurizing condition at the time of pressure bonding is preferably 0.01 to 2 MPa, more preferably 0.02 to 1.5 MPa, and further preferably 0.05 to the welding surface.
- a pressure of ⁇ 1 MPa is applied.
- a pressure of 0.01 MPa or more is preferable because good bonding strength can be easily obtained, and the thermoplastic carbon fiber composite material does not easily spring back during heating, so that the shape is easily maintained and the material strength is increased. Further, if the pressure is 2 MPa or less, it is preferable that the pressurized portion is not easily crushed, the shape is easily retained, and the material strength is increased.
- thermoplastic resin layer disposed between the metal and the thermoplastic carbon fiber composite material may be previously bonded to either the metal or the thermoplastic carbon fiber composite material in advance to form a thermoplastic resin layer.
- a thermoplastic resin layer is first provided on the surface of a metal having irregularities by heating and pressure bonding, and then the thermoplastic resin layer and the joining portion of the thermoplastic carbon fiber composite material are heated and pressure bonded.
- a method that is, a method of sequentially performing the above steps (i) to (iii) can be employed.
- the metal surface, a thermoplastic resin layer such as a film and a nonwoven fabric, and a thermoplastic carbon fiber composite material are heated in a laminated state, and the bonding is performed at once, that is, the step (ii) ) And (iii) may be performed as one step.
- steps (ii) and (iii) simultaneously include, for example, coating a molten film of a thermoplastic resin directly on a metal and laminating a thermoplastic carbon fiber composite material thereon. The method of doing is mentioned.
- the steps (ii) to (iv) are performed simultaneously or continuously after the step (i) is performed, the molding time can be shortened and the joining member can be manufactured efficiently.
- thermoplastic resin layer disposed between the organic coating layer and the thermoplastic carbon fiber composite material.
- the thermoplastic resin layer may be formed on the surface by previously adhering to either one or both of the metal having the organic coating layer and the thermoplastic carbon fiber composite material in advance.
- the thermoplastic resin layer is bonded and formed only on one side, it is preferably formed on the side of the metal surface on which the organic coating layer is formed.
- the temperature when the thermoplastic resin layer is adhered and arranged on the surface of the metal or thermoplastic carbon fiber composite material on which the organic coating layer has been formed in advance is the melting temperature of the thermoplastic resin + 15 ° C.
- the thermoplastic resin layer can be used in the form of a film, a sheet, or a non-woven fabric, and can be disposed by thermocompression bonding to a desired surface, or by applying a molten resin thinly by injection molding or extrusion molding.
- the metal surface temperature when the hot-melt thermoplastic resin layer is brought into contact with the metal having the organic coating layer is higher than the melting temperature of the thermoplastic resin + 15 ° C. and the decomposition temperature ⁇ 30, as in the case without the organic coating layer. It is preferable that the temperature is lower than ° C. If the surface temperature of the metal is less than the above range, the resin may not be familiar with the surface, and if it exceeds the above range, decomposition of the resin may proceed. Further, the time for maintaining such a temperature is preferably as short as possible as long as the time for essential bonding between the composite material and the metal can be secured, and for example, about 10 seconds to 10 minutes is appropriate.
- the affinity by the organic coating layer such as the triazine thiol derivative-containing layer on the metal surface is important, and in general, the organic coating layer may be altered by high temperatures. High temperatures are not preferred.
- the joining time at 275 ° C. is preferably about 10 minutes or less.
- thermoplastic resin layers having a form such as a film, a sheet, or a nonwoven fabric are laminated between the metal bonding surface having the organic coating layer and the composite material, and the melting temperature of the thermoplastic resin + 15 ° C.
- the whole can be thermocompression-bonded to produce a joined body at once.
- the decomposition temperature ⁇ 30 ° C.
- thermoplastic resin layer comes into contact with the uneven portion of the metal surface by heating at the time of joining, and particularly enters into the recessed portion and solidifies, so that the joining strength with the metal is increased by the so-called anchor effect. it is conceivable that.
- the thermoplastic resin on at least the surface (contact surface) of the composite material in the joint is also melted by heating and melting at the time of joining, so that the resin in the thermoplastic resin layer is in intimate contact.
- the metal and the composite material are pressurized and the whole is pressure-bonded so that the metal and the composite material are sufficiently adhered through the molten thermoplastic resin layer, and when the heating is completed, the thermoplastic resin is solidified.
- the whole is integrated. It is surmised that the pressurization at the time of joining contributes to the improvement of adhesive strength because part of the carbon fibers in the composite material can easily enter the recesses.
- the metal having a concavo-convex shape formed in the joint can be once subjected to heat treatment and then used for joining. This heat treatment often increases the bonding strength.
- the heat treatment conditions in this case are preferably a temperature of 250 to 500 ° C. and a time of 10 seconds to 10 minutes.
- thermosetting carbon fiber composite materials with a thermosetting resin as a matrix when bonding to metal, use an adhesive or insert metal into the prepreg and then force molding over a long period in the autoclave. It was done.
- a thermoplastic carbon fiber composite material using a thermoplastic resin as a matrix is used, a molded body having a desired shape can be manufactured by press molding or the like. Therefore, such molding can be performed simultaneously or continuously with the bonding of the carbon fiber composite material and the metal. That is, this invention includes the manufacturing method of the joining member which consists of a metal composite molded object with which the thermoplastic carbon fiber composite material and the metal were joined by performing joining and shaping
- thermoplastic resin layer provided between the fiber composite material, not only can the metal and the carbon fiber composite material be strongly bonded, but also the bonding and molding can be performed simultaneously or continuously to shorten the efficiency.
- a metal composite compact can be manufactured in time.
- molding and joining in the production of the joining member can be performed simultaneously in a short time, it is industrial compared to the case of using a conventional carbon fiber composite material with a thermosetting resin as a matrix. It is a superior method.
- a method for manufacturing a joining member obtained by joining a carbon fiber composite material having a thermoplastic resin matrix and a metal a depth of 0.02 to Forming a plurality of 0.6 mm recesses, forming a thin layer of triazine thiol derivative on the metal surface, and fusing a thermoplastic resin layer on the thin layer of triazine thiol derivative on the metal surface.
- thermoplastic resin layer having a thickness in the range of 5 ⁇ m to 5 mm, and laminating a thermoplastic carbon fiber composite material on the thermoplastic resin layer to form a thin layer of metal / triazine thiol derivative /
- a joining member in which the thermoplastic carbon fiber composite material and the metal are firmly joined is obtained.
- One mode (cross-sectional view) of the joining member obtained in the present invention is shown in FIG.
- the bonding strength when the tensile test is performed at a tensile speed of 1 mm / second at the bonded portion is preferably 5 MPa or more, and when bonded under particularly preferable conditions, a bonding strength exceeding 10 MPa can be realized.
- the bonding strength can be evaluated by a tensile test, but the upper limit of the bonding strength is substantially about 50 MPa. Therefore, the joining member of the thermoplastic carbon fiber composite material and metal obtained in the present invention can be suitably used as a structural member that requires a sufficient joining strength. Examples of such a structural member include parts constituting moving bodies such as automobiles, bicycles, railway vehicles, airplanes, and ships, structural materials for buildings and furniture, materials for sports equipment, and the like.
- the number of joining points of the joining member is not limited, and can be arbitrarily selected depending on the joining environment, whether single wrap or double wrap. In the case of double wrap, the bonding area is doubled, so the bonding strength is also doubled.
- thermoplastic carbon fiber composite materials and nonwoven fabrics used in the examples and comparative examples are manufactured by the method described in the following reference examples.
- thermoplastic carbon fiber composite material (I) of continuous laminated fiber of 0 ° and 90 ° continuous carbon fiber (“Tenax” (registered trademark) STS40-24KS manufactured by Toho Tenax Co., Ltd.) (average fiber diameter 7 ⁇ m, tensile strength 4000 MPa) 64 layers are laminated so that layers of 0 degree and 90 degrees are alternately arranged while sequentially laminating strands of nylon and nylon 6 film (“Emblem” (registered trademark) ON25 ⁇ m thickness) manufactured by Unitika Ltd.) (64 layers of carbon fiber and 65 layers of nylon 6 film), heated and compressed for 20 minutes at a temperature of 260 ° C.
- thermoplastic carbon fiber composite material (II-A) from isotropic random mat Carbon fiber cut to an average fiber length of 20 mm (“Tenax” (registered trademark) STS40, manufactured by Toho Tenax Co., Ltd., average fiber diameter: 7 ⁇ m) Isotropic random mat formed into a sheet shape in a random arrangement state so as to have an average basis weight of 540 g / m 2 (between the unit KE435-POG (nylon 6) cloth), the random mat / nylon It is sandwiched so as to be repeatedly laminated with 6 cloths, pressed at a temperature of 260 ° C.
- thermoplastic resin was present in the thermoplastic carbon fiber composite material in an amount of 120 parts by weight with respect to 100 parts by weight of the carbon fiber.
- thermoplastic carbon fiber composite material (II-B) from isotropic random mat “Tenax” (registered trademark) STS40-24KS (average fiber diameter 7 ⁇ m, tensile strength 4000 MPa) manufactured by Toho Tenax Co., Ltd. as carbon fiber Carbon fiber strands were used. This is cut into a predetermined length by a method described in International Publication No. 2012/105080, and a fixing net equipped with a lower suction device via a fiber opening device (gas blowing nozzle) and a flexible transport pipe Two kinds of isotropic random mats having different average fiber lengths, opening degrees and the like shown in Table 1 below were prepared.
- thermoplastic carbon fiber composite material was 120 parts by weight for sample 1 with respect to 100 parts by weight of carbon fiber and 100 parts by weight for sample 2 with respect to 100 parts by weight of carbon fiber. It was.
- thermoplastic carbon fiber composite material (II-C) from isotropic random mat
- carbon of “Tenax” (registered trademark) STS40-24KS average fiber diameter 7 ⁇ m, strand width 10 mm
- Fiber strands were used. This is slit by a longitudinal slitting device to a strand width of 0.8 mm by a method described in JP 2013-49208 A (Japanese Patent Application No. 2011-188768), and then a rotary cutter having a spiral knife disposed on the surface. The fiber length was cut to 20 mm or 25 mm.
- the strand that passed through the cutter was introduced into a flexible transportation pipe arranged immediately below the rotary cutter, and subsequently introduced into a fiber opening device (gas blowing nozzle) continuously provided at the lower end of the transportation pipe.
- a fiber opening device gas blowing nozzle
- nipples made of SUS304 having different diameters were welded to produce a double pipe.
- a small hole was provided in the inner tube of the double tube, and compressed air was supplied between the inner tube and the outer tube with a compressor. At this time, the wind speed from the small hole was 450 m / sec.
- a taper pipe whose diameter increases downward is welded to the lower end portion of the double pipe so that the carbon fiber cut in the taper pipe moves downward along with the air flow.
- Matrix resin was supplied into the tube from the hole provided on the side surface of the tapered tube.
- matrix resin particles of nylon 6 resin “A1030” manufactured by Unitika Ltd. were used.
- an air-permeable support body (hereinafter referred to as “fixing net”) that moves in a certain direction is installed below the outlet of the taper pipe, and suction is performed from below by a blower.
- fixing net an air-permeable support body
- the carbon fiber supply rate was set to 212 g / min
- the matrix resin supply rate was set to 320 g / min
- the apparatus was operated.
- the carbon fiber and the thermoplastic resin were randomly mixed on the fixing net.
- a mat was formed.
- the basis weight of carbon fibers of this random mat was 265 g / m 2 .
- the nylon 6 resin particles were uniformly dispersed in the carbon fiber with almost no spots. In this way, random mats of the kind shown in Table 2 below were prepared.
- thermoplastic carbon fiber composite material (II-C) was obtained.
- the thermoplastic resin present in the thermoplastic carbon fiber composite material was 120 parts by weight for sample 3 with respect to 100 parts by weight of carbon fiber for sample 3 and 100 parts by weight for 100 parts by weight of carbon fiber for sample 4. It was.
- a nylon 6 nonwoven fabric was produced by a melt blow method using a nylon 6 resin “Novamid” (registered trademark) 1010C2 (melting temperature 225 ° C.) manufactured by DSM Japan Engineering Plastics Co., Ltd. as a raw material.
- the melt blow method adopted here discharges molten polymer from a plurality of arranged orifice dies, and injects a high-speed gas from an injection gas port installed adjacent to the orifice die to make the discharged molten polymer fine fiber.
- the nonwoven fabric is produced by collecting the fiber stream on a conveyor net as a collector.
- the obtained nylon 6 nonwoven fabric had an average fiber diameter of 5 ⁇ m, an average basis weight per sheet of 20 g / m 2 , an average bulk density of 0.1 g / cm 3 , and an average thickness of 0.2 mm.
- Example 1 One side of a 100 mm long, 25 mm wide, 1.6 mm thick SPCC plate (cold rolled steel plate) is degreased and dried with acetone, and then a YAG laser with an oscillation wavelength of 1.064 ⁇ m, a maximum rated output of 20 W, and a beam spot of 130 ⁇ m (continuation) Wave) was used to form lattice-shaped grooves having a laser spot center interval of 0.08 mm and a depth of 0.08 mm over the entire surface to be joined to the thermoplastic carbon fiber composite material.
- thermoplastic carbon fiber composite material (I) using the continuous fiber obtained in Reference Example 1 is cut into a length of 100 mm and a width of 25 mm, and the surface is 25 mm ⁇ 25 mm in a single wrap with the SPCC plate having the nylon 6 layer on the surface. Overlaying in a range, putting it in a mold, heating and pressurizing in the mold at a temperature of 250 ° C. and a pressure of 0.2 MPa for 5 minutes, and melting the nylon 6 layer, the thermoplastic carbon fiber composite material and SPCC The joining member with the board was created. When five such joining members were prepared and a tensile test was performed at a speed of 1 mm / min with an Instron 5587 universal testing machine, the average value of the joining strength was 13 MPa.
- Example 2 Laser processing was performed on the entire surface of one side of a 590 MPa class high tensile material having a length of 100 mm, a width of 25 mm, and a thickness of 1.6 mm in the same manner as in Example 1 to form a lattice-shaped groove having a depth of 0.08 mm.
- Nylon 6 film (“Emblem” (registered trademark) ON, manufactured by Unitika Co., Ltd., ON, 25 ⁇ m thickness, melting temperature 225 ° C) 20 layers were laminated and installed on one side, and then the high tension material was heated to 250 ° C by electromagnetic induction heating. And immediately cooled to room temperature.
- the nylon film was melted, adhered, and solidified to form a nylon 6 layer having a thickness of 500 ⁇ m on one surface of the high-tensile material.
- a flat plate of thermoplastic carbon fiber composite material (II-A) made of a random mat obtained in Reference Example 2A was cut into a length of 100 mm and a width of 25 mm, and this was cut into 25 mm in a single wrap with the high-tensile material having the above nylon 6 layers.
- the composite material was superposed within a range of 25 mm, the composite material was heated to 250 ° C., the high-tensile material was heated to 140 ° C., and heated and pressurized at 0.2 MPa for 1 minute using a mold.
- the high-tensile material was heated to 250 ° C. by electromagnetic induction heating, and heated and pressurized at 0.2 MPa for 1 minute to prepare a joining member of the thermoplastic carbon fiber composite material and the high-tensile material.
- the average value of the joining strength was 10 MPa.
- Example 3 A SPCC plate having a lattice-shaped groove having a depth of 0.08 mm formed on one side by laser processing similar to that in Example 1 was heat-treated at 300 ° C. for 10 minutes, and then a nylon having a thickness of 0.05 mm was formed on the surface thereof.
- a joining member of the thermoplastic carbon fiber composite material (I) and SPCC was prepared in the same process as in Example 1 except that 6 layers were formed. When five such joining members were prepared and a tensile test was performed at a speed of 1 mm / min with an Instron 5587 universal testing machine, the average value of the joining strength was 12 MPa.
- Example 4 The surface of the aluminum plate was the same as in Example 1 except that a 1mm-thick No. 5052 aluminum plate (having a lattice-like groove with a depth of 0.08 mm formed on one side by laser processing) was used instead of the SPCC plate. 6 layers of nylon having a thickness of 50 ⁇ m were formed. A flat plate of thermoplastic carbon fiber composite material (II-A) made of a random mat obtained in Reference Example 2A was cut into a length of 100 mm and a width of 25 mm, and this was cut with an aluminum plate having the above nylon 6 layer and a single wrap.
- II-A thermoplastic carbon fiber composite material
- the carbon fiber composite material and the 5052 aluminum plate joined member were prepared by overlapping the layers in a range of 25 mm ⁇ 25 mm and heating and pressing at 250 ° C., 0.2 MPa for 5 minutes using a mold.
- a tensile test was performed at a speed of 1 mm / min with an Instron 5587 universal testing machine, the aluminum plate portion was destroyed.
- the bonding strength was 7.1 MPa or more.
- Example 5 Instead of performing laser processing on the entire surface of one side of SPCC (cold rolled steel sheet), fine dents with an average diameter of 100 ⁇ m and a depth of 60 ⁇ m are made by sandblasting so that the total area of the dents relative to the metal surface area of the joint is 20% Then, after forming a large number, a joined member of the thermoplastic carbon fiber composite material (I) and SPCC was prepared in the same manner as in Example 1 except that heat treatment was performed at 300 ° C. for 10 minutes. When five such joining members were prepared and a tensile test was performed at a speed of 1 mm / min with an Instron 5587 universal testing machine, the average value of the joining strength was 12 MPa.
- Example 6 A 1.6 mm thick 90 mm ⁇ disk-shaped SPCC material was used, and irregularities formed by laser processing were formed on one side of the SPCC material in the same manner as in Example 1, and a nylon 6 film (“Emblem” manufactured by Unitika Ltd.) was applied to the laser processed side. (Registered trademark) ON, 25 ⁇ m thick, melting temperature 225 ° C.) were installed, and then the SPCC material was heated to 250 ° C. by electromagnetic induction heating and immediately cooled to room temperature. The nylon 6 film was melted, adhered, and solidified to form a nylon 6 layer having a thickness of 0.05 mm on the SPCC disk. Next, the mold capable of forming the hat of FIG.
- Example 7 Laser processing was performed on both surfaces of SPCC (cold rolled steel sheet) having a length of 100 mm, a width of 25 mm, and a thickness of 1.6 mm in the same manner as in Example 1, and the laser spot center interval was 0.08 mm and the depth was 0.08 mm. Then, an organic coating layer was formed on the surface as follows. In the formation of this organic coating layer, the above metal plate having grid-like grooves on both sides was degreased in a sodium hydroxide aqueous solution having a concentration of 15.0 g / L and a temperature of 60 ° C. for 60 seconds, followed by washing with water for 60 seconds. And dried in an oven at 80 ° C. for 30 minutes.
- a metal compound film mainly composed of a metal phosphate and a hydroxide was formed on both surfaces of the metal plate.
- a metal plate having a metal compound film was immersed in an ethanol / water (volume ratio 95/5) solution of triethoxysilylpropylaminotriazinethiol monosodium having a concentration of 0.7 g / L at room temperature for 30 minutes.
- a mold was used to heat and press at 250 ° C., 0.2 MPa for 5 minutes to prepare a joining member of the thermoplastic carbon fiber composite material and the SPCC plate.
- a tensile test was performed at a speed of 1 mm / min with an Instron 5587 universal testing machine, the average value of the joining strength was 13 MPa.
- Example 8 A SPCC plate (cold rolled steel plate) having a length of 100 mm, a width of 25 mm, and a thickness of 1.6 mm, which was surface-treated with laser processing and a triazine thiol derivative in the same manner as in Example 7, was prepared, and this was raised to 240 ° C. After warming, two nylon 6 nonwoven fabrics obtained by the melt blow method obtained in Reference Example 3 were laminated on the upper surface of the SPCC. Also, two types of composite materials (II-B, Sample 1 and Sample 2 in Table 1) using the isotropic random mat material obtained in Reference Example 2B as the carbon fiber composite material were 100 mm in length and 25 mm in width, respectively. And dried at 80 ° C. for 5 hours.
- a plate-like joined body obtained by joining a thermoplastic carbon fiber composite material and SPCC via a nylon 6 resin layer having a thickness of 400 ⁇ m by heating and pressurizing for 5 minutes under a condition of 5 MPa to melt the nylon 6 nonwoven fabric. Created. Five pieces of each of these joined bodies were prepared, and each was subjected to a tensile test in the same manner as in Example 7 and measured. The results are shown in Table 1.
- Example 9 An SPCC plate (cold rolled steel plate) having a length of 100 mm, a width of 25 mm, and a thickness of 1.6 mm was subjected to uneven formation and surface treatment with a triazine thiol derivative in the same manner as in Example 7, and then heated to 240 ° C. .
- Two nylon 6 films (“Emblem” (registered trademark) ON, 25 ⁇ m thickness, manufactured by Unitika Ltd.) were installed on the upper surface of the SPCC plate.
- carbon fiber composite materials II-C, samples 3 and 4 in Table 2 using two types of isotropic random mat materials shown in Table 2 obtained by the method of Reference Example 2C were each 100 mm in length.
- thermoplastic carbon fiber composite material and a metal can be joined firmly and stably by a simple method. Furthermore, since the carbon fiber composite material and the metal are bonded via the thermoplastic resin, it is possible to simultaneously prevent electrolytic corrosion caused by the carbon fibers. And the joining member of a carbon fiber composite material and a metal can be obtained easily and in a short time. Moreover, since joining and shaping
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Abstract
Description
一方、マトリックスとして熱可塑性樹脂を用いた炭素繊維複合材料(以下、「熱可塑性炭素繊維複合材料」もしくは単に「複合材料」ということがある)は、熱可塑性樹脂が相溶する範囲内においては材料同士が溶着により接合し、マトリックス樹脂同士の接合体並みの接合強度が期待できる。しかしながら、熱可塑性炭素繊維複合材料であってもマトリックス樹脂の溶着(融着)による金属との接合は困難であることが多い。
さらに、熱硬化性樹脂をマトリックスとする熱硬化性炭素繊維複合材料については、特許文献7に金属と該複合材料との双方に親和性のある中間樹脂層を配置して接合する方法が記されている。
しかしながら、特許文献2,3に記された熱可塑性樹脂と金属との接合方法により接合しようとしても、熱可塑性炭素繊維複合材料ではマトリックスの熱可塑性樹脂が炭素繊維束に「滲みこんだ」状態にあるため、その表面に必ずしも均質に熱可塑性樹脂が存在するわけではなく、なかには熱可塑性樹脂の「欠乏した」部分が存在するため、充分な接合強度が発現しなかったり、接合強度が大きくばらついたりする懸念がある。また炭素繊維は金属に対していわゆる電蝕の原因となるため、マトリックス樹脂が欠乏した部分においては炭素繊維が金属に直接触れることにより金属を腐食させる原因となっている。
熱可塑性樹脂をマトリックスとする炭素繊維複合材料と金属とを接合させてなる接合部材を製造する方法であって、
接合部の金属表面に深さ0.02~0.6mmの凹凸形状を形成させる工程(i)と、
金属と複合材料の間の接合部に厚さが5μm以上5mm以下の範囲にある熱可塑性樹脂層を設ける工程(ii)と、
該接合部を加熱して該熱可塑性樹脂層を溶融させることにより金属と炭素繊維複合材料とを強固に接合する工程(iii)と、を含む、接合部材の製造方法である。
また、接合と成形とを同時にあるいは連続して同一金型内で行うこともできるので、これらを同時に又は連続的に行えば、所望形状に成形した炭素繊維複合材料と金属との接合体(金属複合成形体)を少ない工程でかつ短時間で製造することが可能となる。
接合部の金属表面に深さ0.02~0.6mmの凹凸形状を形成させる工程(i)と、
金属と炭素繊維複合材料の間の接合部に厚さが5μm以上5mm以下の範囲にある熱可塑性樹脂層を設ける工程(ii)と、
該接合部を加熱して該熱可塑性樹脂層を溶融させることにより金属と熱可塑性炭素繊維複合材料とを強固に接合する工程(iii)と、
を含むものである。
本発明で金属との接合に用いる熱可塑性炭素繊維複合材料とは、熱可塑性樹脂をマトリックスとし、かかるマトリックス中に強化繊維として炭素繊維を含有する複合材料である。
ここで、熱可塑性炭素繊維複合材料は、炭素繊維100重量部に対し熱可塑性樹脂が50~1000重量部含まれていることが好ましい。より好ましくは、炭素繊維100重量部に対し、熱可塑性樹脂50~400重量部、更に好ましくは、炭素繊維100重量部に対し、熱可塑性樹脂50~100重量部である。熱可塑性樹脂が炭素繊維100重量部に対し50重量以上であれば、マトリックス樹脂から露出したドライの炭素繊維が増加しにくいため好ましい。また、熱可塑性樹脂が炭素繊維100重量部に対し熱可塑性樹脂が1000重量部以下であれば、炭素繊維が適切な量含まれるため構造材料として適切となり好ましい。
これらの熱可塑性樹脂は、必要に応じて、安定剤、難燃剤、顔料、充填剤等の添加剤を含んでも差し支えない。
熱可塑性炭素繊維複合材料における炭素繊維の形態としては、特に限定されず、不(非)連続な繊維でも連続した繊維でもよい。連続繊維の場合は、織物であっても、繊維を一方向に配置してシート状としたもの、例えば連続繊維のストランドを積層したいわゆるUDシートであってもよい。繊維を一方向に配置したものを積層する場合は、各層の繊維配列方向を変えて多層に積層することができ、例えば直交方向に交互に積層することができる。また積層面を厚さ方向に対称に配置したものでもよい。
臨界単糸数=600/D (a)
0.7×104/D2<N<1×105/D2 (b)
(ここでDは炭素繊維の平均繊維径(μm)である)
ここでいう「二次元等方性ランダムマット」とは、不連続炭素繊維が水平な面内においてランダムな方向に配置されており、面内で方向性がない均質なマットのことをいう。このような二次元等方性ランダムマットに均一に熱可塑性樹脂を溶融含浸させることにより等方性の熱可塑性炭素繊維複合材料を得ることができる。
なお、上記の方法において、ネットコンベヤ上に、熱可塑性樹脂からなる不織布を配置し、不織布をネットコンベヤと共に移動させることにより、不織布上に炭素繊維を含む等方性ランダムマットを形成することも可能である。
本発明に用いる金属としては、具体的には鉄、ステンレス、アルミニウム、銅、黄銅、ニッケル、亜鉛等の金属又はこれらの合金が挙げられる。なかでも、金属が鉄及びアルミニウムより選択される少なくとも1種を含むことが好ましく、金属を構成する元素が鉄又はアルミニウムを主とするものがより好ましい。ここで「主とする」とは、含有量が90重量%以上を占めることを意味する。特にSS材(一般構造用圧延鋼材)、SPCC材(冷間圧延鋼材)、ハイテン材(高張力鋼材)等の鉄類や、SUS304、316等のステンレス類、1000~700番台アルミニウムやその合金が好ましく用いられる。接合しようとする金属部材の形状にはとくに限定はなく、得ようとする接合部材に合わせて適宜選択できる。
なお、これらの金属部材は2種以上の金属を含むものでもよく、また、少なくとも表面が金属を含む部材であればよく、表面に金属メッキが施されたものでも差し支えない。また、その形状も、熱可塑性炭素繊維複合材料との接合に必要な面が確保される限り、平板状のみに限定されず、任意の形状としたものを使用でき、例えば、L字型、T字型、H字型、コ字型、へ字型等の断面や円筒形にした金属部材でもよく、また、曲面を有するものでもよい。
工程(i)において、接合しようとする金属は、その接合部となる表面の一部又は全部に、深さ0.02~0.6mm、好ましくは深さ0.05~0.5mmの凹凸を形成する。この凹凸は、例えば、金属表面にレーザー照射、ブラスト、研磨、切削、ヤスリ加工又は化学処理を施すことにより形成することができる。このように金属表面に凹凸を形成することにより、熱可塑性複合材料と金属とを接合させる際に、金属表面の凹凸の凹部内に、加熱によって溶融した熱可塑性樹脂が入り込み、より高い接合強度が得られる。
レーザー照射により凹凸を形成する場合は、例えば20W機種のレーザービームスポット径をΦ0.02~0.6mmに絞り、レーザースポット中心間距離0.02~0.6mm間隔で格子状に、深さ0.02~0.6mmのU字型断面又はV字型断面をもつ溝を形成させることができる。この場合の溝幅は0.05~0.5mmが好ましい。
レーザー処理に際しては、とりわけ波長300nm~1,100nmのレーザー光を50W/mm2以上の強度で金属の表面に照射することが好ましい。このようなレーザー光の照射条件を採用することによって、金属の強度の低下を抑制し、凹凸形状を均一に形成することができる。上記溝の深さや幅はレーザー処理条件の選定によって調節可能である。
ここで、用いることのできるレーザーとしては、固体レーザー、液体レーザー、ガスレーザー、半導体レーザー、化学レーザー等様々なものが適用できるが、固体レーザーでは例えばYAG(イットリウム・アルミニウム・ガーネット)レーザーやサファイアレーザー、ガスレーザーでは炭酸ガスレーザーやヘリウムネオンレーザーを挙げることができる。
本発明の接合部材の製造方法は、凹凸を形成した金属表面に有機被覆層を設ける工程(i-A)を含んでもよい。工程(i-A)は、凹凸を形成した金属表面と熱可塑性樹脂層の間に有機被覆層を設ける工程であることが好ましく、工程(i)と工程(ii)の間に行われることが好ましい。工程(i-A)により、凹凸を形成させた金属表面に、金属と熱可塑性樹脂層との接合力を強化させる有機化合物を塗布、浸漬等により付与して乾燥処理する方法や電気化学的な方法等により、金属の接合しようとする表面に予め有機化合物の薄層(以下「有機被覆層」ということがある)を形成して、接合に供することができ、これにより、接合部の金属と熱可塑性樹脂層との接着性をより一層向上させることができる。上記有機被覆層としては、トリアジンチオール誘導体を含む層が好ましい。
この有機被覆層は必ずしも接合する金属全面に形成する必要はなく、また、厚さもとくに制限はなく、接着性が確保できればよい。有機被覆層の平均厚さは、好ましくは、0.005~10μmである。
かかるトリアジンチオール誘導体含有層と金属との間に、水酸化物、カルボン酸塩、リン酸塩、硫酸塩等の金属化合物層を含むことが、更なる接合強度向上が期待できるため好ましい。金属化合物層を形成する方法としては国際公開第2009/157445号に記載の方法が好ましく挙げられるが、具体的には接合しようとする金属の表面にトリアジンチオール誘導体含有層を形成するに先立ち、塩酸、硫酸、リン酸等の酸に金属を浸漬するか、金属の表面に塗布し、乾燥する方法が挙げられる。
本発明は熱可塑性樹脂をマトリックスとする炭素繊維複合材料と、深さ0.02~0.6mmの凹凸形状を形成させた金属表面との間に、厚さが5μm~5mm、好ましくは20μm~4mm、さらに好ましくは40μm~3mmの範囲にある熱可塑性樹脂層を設け、接合部を加熱して該熱可塑性樹脂層を溶融させることにより金属と熱可塑性炭素繊維複合材料とを接合させる。
上記熱可塑性樹脂層は、熱可塑性樹脂から実質的になる少なくとも1枚の、熱溶融性のフィルム、シート、織物、不織布、又は粉を含有する層から形成されることが好ましく、なかでもフィルム、シート、又は不織布を含有する層から形成されることがより好ましい。ここで、「実質的に」とは、熱可塑性樹脂の他に、必要に応じて(全体の20重量%以下の割合で)、例えば、安定剤、難燃剤、顔料、充填剤、可塑剤、溶融粘度調節剤等の添加剤を含んでも差し支えないことをいう。熱可塑性樹脂層は、フィルム、シート、織物、不織布又は粉状の形態で用いて、金属又は熱可塑性炭素繊維複合材料の表面に熱圧着させたり、溶融した熱可塑性樹脂を射出成形あるいは溶融押出成形等により金属又は熱可塑性炭素繊維複合材料の表面に薄く貼り付けたり積層することで配置することができる。
これらの熱可塑性樹脂は、必要に応じて、安定剤、難燃剤、顔料、充填剤、可塑剤、溶融粘度調節剤等の添加剤を含んでも差し支えない。
ここで、熱可塑性樹脂層の厚さは、熱可塑性樹脂層が実質的にフィルム、シート、不織布等からなる場合は、それらの溶融前の厚さを言い、複数積層される場合は、積層後の合計の厚さを指す。
熱可塑性樹脂層となるフィルム、シート、不織布等を、予め金属の凹凸面と複合材料表面の少なくとも一方、好ましくは金属の凹凸面、に接触させた状態で加熱溶融させた後、冷却固化させることにより、その表面に均質な熱可塑性樹脂層を形成させることもできる。接合する金属あるいは複合材料の表面に熱可塑性樹脂層を形成させる工程の温度は、熱可塑性樹脂の溶融温度+15℃以上で分解温度-30℃以下の範囲であることが好ましく、溶融温度+20℃以上で分解温度-20℃以下の温度範囲がより好ましい。例えば、熱可塑性樹脂がPA6(融点220℃)の場合は、235~300℃が好ましい温度である。なお、ここでいう「溶融温度」とは、熱可塑性樹脂層を構成する樹脂の融点であり、融点の無いものについては十分な流動性を開始する温度である。金属の凹凸面に上記のフィルム、シート、不織布等を接触させ加熱溶融させることで熱可塑性樹脂層を形成する場合は、予め上記温度に加熱した金属上にフィルム、シート、不織布等を積層して融着させる方法あるいは金属上に熱可塑性樹脂層を積層後に金属を加熱して融着させる方法等が好ましく用いられる。
この場合、金属の表面温度が上記範囲未満であると熱可塑性樹脂が表面に馴染みにくい場合があり、また上記範囲を超えると熱可塑性樹脂の分解が進むことがある。さらに、かかる温度を維持する時間は、熱可塑性炭素繊維複合材料と金属との本質的な接合のための時間が確保できるならば極力短い方がよく、例えば10秒~10分程度が好ましい。
また、溶融した熱可塑性樹脂を金属の凹凸面と複合材料表面の少なくとも一方に直接コーティングして接合面に熱可塑性樹脂層を形成してもよい。
本発明では、熱可塑性樹脂層を実質的に不織布からなる層とすることもできる。この場合、熱可塑性炭素繊維複合材料と凹凸形状を有する金属部材表面との間に、熱可塑性樹脂製の不織布を介在させ、加熱して該不織布を構成する熱可塑性樹脂を溶融させることにより、金属表面と熱可塑性炭素繊維複合材料とを接合させることが好ましい。ここで用いる不織布は、加熱により溶融して金属と接着する熱可塑性樹脂で構成される。上述した熱可塑性樹脂のなかでも、例えば、熱溶融性のポリアミド(ナイロン)、ポリカーボネート、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ポリエチレンナフタレート、ポリエチレン、ポリプロピレン等が好ましい。なかでも、コストと物性の兼ね合いからポリアミド、ポリプロピレンがより好ましい。また、ポリアミド(PAと略記することがある)としては、PA6、PA66又はこれらを主成分とする共重合体、ブレンドが特に好ましい。これらの不織布構成樹脂は、必要に応じて、安定剤、難燃剤、顔料、充填剤等の添加剤を含んでも差し支えない。
なお、ここで言う不織布の「総目付け量」「総嵩密度」とは、それぞれ、不織布全体の目付け量、嵩密度のことであり、熱可塑性樹脂層が1枚の不織布からなるときは、その不織布の目付け量、嵩密度となるが、複数の不織布を積層して熱可塑性樹脂層を構成する場合は、積層した各不織布の目付け量、嵩密度の合計となる。
本発明の接合部材の製造方法においては、凹凸を形成させた金属表面と炭素繊維複合材料間に熱可塑性樹脂層を設けた状態で、加熱することにより上記熱可塑性樹脂層を溶融させ、好ましくはそれと同時に全体を加圧することにより金属と炭素繊維複合材料とを接合させる。
本発明では、上記工程(i)、(ii)、(iii)を順に行ってもよく、工程(i)の後、工程(ii)と(iii)とを一つの工程として行なってもよい。後者は製造工程が簡略化され生産性に優れている。また、上記工程(i)の後に有機被覆層を形成する工程を加え、上記工程(i)、(i-A)、(ii)、(iii)を順に行ってもよい。
溶融された熱可塑性樹脂層は、熱可塑性炭素繊維複合材料と接し、圧着させることで強度がより良好な接合体を与えることができる。
本発明では、熱可塑性樹脂層と熱可塑性炭素繊維複合材料とを、上記工程(iii)中で圧着させるが、接合した後、必要に応じ、さらに加熱下で加圧し圧着させる工程(iv)を行なうことができる。
熱硬化性樹脂をマトリックスとした熱硬化性炭素繊維複合材料では、金属と接合しようとする場合に、接着剤を用いたり、プリプレグ中に金属をインサートした後オートクレーブ中での長時間にわたる成形を強いられていた。これに対し、本発明は、熱可塑性樹脂をマトリックスとした熱可塑性炭素繊維複合材料を用いているため、プレス成形等によって所望の形状の成形体を製造できる。したがって、炭素繊維複合材料と金属の接合同時にあるいは連続して、このような成形も行うことができる。すなわち、本発明は、型内で接合と成形とを同時に行うことにより、熱可塑性炭素繊維複合材料と金属とが接合された金属複合成形体からなる接合部材の製造方法を包含する。例えば、上記工程(iii)を所定形状のキャビティーを備える型内で実施することにより、接合と成形とを同時に実施することができるため、短時間で容易に金属複合成形体を得ることも可能である。
各実施例等に記載のとおりの熱可塑性炭素繊維複合材料-金属部材接合体(接合部材)を5枚ずつ作成し、それぞれについて、「インストロン(登録商標)5587」万能試験機により、引っ張り速度1mm/分で引っ張り試験を行って求めた引っ張り強度の平均値を、当該接合体の接合強度の値とした。
参考例2B及び参考例2Cにより得たランダムマット材の繊維束分析は、国際公開第2012/105080号に記載された方法に準じて実施した。
連続繊維0度90度交互積層材の熱可塑性炭素繊維複合材料(I)の製造
炭素繊維(東邦テナックス(株)製「テナックス」(登録商標)STS40-24KS(平均繊維径7μm、引張強度4000MPa)のストランドとナイロン6フィルム(ユニチカ(株)製「エンブレム」(登録商標)ON25μm厚)とを順次積層しながら、繊維方向0度の層と90度の層が交互に配置するように64層積層し(炭素繊維64層でナイロン6フィルム65層)、これを温度260℃、圧力2MPaで、20分間加熱圧縮し、繊維が0度90度交互、対称積層、炭素繊維体積率(Vf)47%(質量基準の炭素繊維含有率57%)、厚さ2mmの平板状熱可塑性炭素繊維複合材料(I)を作成した。該熱可塑性炭素繊維複合材料における、熱可塑性樹脂の存在量は、炭素繊維100重量部に対し、75重量部であった。
等方性ランダムマットからの熱可塑性炭素繊維複合材料(II-A)の製造
平均繊維長20mmにカットした炭素繊維(東邦テナックス(株)製「テナックス」(登録商標)STS40、平均繊維径7μm)を平均目付け540g/m2となるようランダムな配列状態でシート状に形成した等方性ランダムマットを(ユニチカ(株)製KE435-POG(ナイロン6)クロス)の間に、該ランダムマット/ナイロン6クロスの繰り返し積層となるように挟みこんで、温度260℃、圧力2.5MPaでプレスし、炭素繊維体積率35%(質量基準の炭素繊維含有率45%)、厚さ2mmの平板状熱可塑性炭素繊維複合材料(II-A)を作成した。該熱可塑性炭素繊維複合材料における、熱可塑性樹脂の存在量は、炭素繊維100重量部に対し、120重量部であった。
等方性ランダムマットからの熱可塑性炭素繊維複合材料(II-B)の製造
炭素繊維として東邦テナックス(株)製「テナックス」(登録商標)STS40-24KS(平均繊維径7μm、引張強度4000MPa)の炭素繊維ストランドを用いた。これを国際公開第2012/105080号に記載の方法により、所定の長さにカットし、開繊装置(気体吹付けノズル)及びフレキシブルな輸送配管を経由して、下方吸引装置を装備した定着ネット上に堆積させ、後掲の表1に示す平均繊維長、開繊度等の異なる2種の等方性ランダムマットを作成した。そして、各ランダムマットを、参考例2Aと同様にユニチカ(株)製KE435-POG(ナイロン6)クロスの間に挟みこんで、温度260℃、圧力2.5MPaでプレスし、表1に示すような炭素繊維体積率の異なる2種の平板状熱可塑性炭素繊維複合材料(II-B)を作成した。該熱可塑性炭素繊維複合材料における、熱可塑性樹脂の存在量は、試料1が炭素繊維100重量部に対し、120重量部であり、試料2が炭素繊維100重量部に対し、100重量部であった。
等方性ランダムマットからの熱可塑性炭素繊維複合材料(II―C)の製造
炭素繊維として、東邦テナックス社製 “テナックス”(登録商標)STS40-24KS(平均繊維径7μm、ストランド幅10mm)の炭素繊維ストランドを用いた。これを、特開2013-49208号公報(特願2011-188768明細書)に記載の方法により、縦スリット装置によりストランド幅0.8mmにスリットした後、螺旋状ナイフを表面に配置したロータリーカッターにより繊維長20mm又は25mmにカットした。カッターを通過したストランドを、上記ロータリーカッターの直下に配置したフレキシブルな輸送配管に導入し、引き続き、輸送配管の下端に連設した開繊装置(気体吹付けノズル)に導入した。この開繊装置としては、径の異なるSUS304製のニップルを溶接し、二重管を製作して使用した。二重管の内側の管に小孔を設け、内側の管と外側の管との間にコンプレッサーにて圧縮空気を送気した。この時、小孔からの風速は450m/secであった。この二重管の下端部には下方に向けて径が拡大するテーパー管を溶接し、該テーパー管内をカットした炭素繊維が空気流とともに下方へ移動するようにした。
上記テーパー管の側面の設けた孔より、マトリックス樹脂を管内に供給した。マトリックス樹脂としてはユニチカ(株)製のナイロン6樹脂“A1030”の粒子を使用した。そして、テーパー管出口の下方に、一定方向に移動する通気性の支持体(以後「定着ネット」と呼ぶ)を設置し、その下からブロワにて吸引を行い、該フレキシブルな輸送配管とテーパー管とを、定速で移動する定着ネットの幅方向に往復運動させながら、テーパー管先端から空気流とともに吐出されるカットした炭素繊維とナイロン樹脂粒子の混合体を、その定着ネット上に帯状に堆積させた。この際、炭素繊維の供給量を212g/min、マトリックス樹脂の供給量を320g/minにセットし、装置を稼動したところ、定着ネット上に炭素繊維と熱可塑性樹脂とが斑なく混合されたランダムマットが形成された。このランダムマットの炭素繊維の目付け量は265g/m2であった。また、ナイロン6樹脂粒子は、炭素繊維中に殆ど斑の無い状態で均一に分散されていた。
このようにして後掲の表2に示す種のランダムマットを作成した。これらのランダムマットを、それぞれ、4枚積層し、金型に入れ、温度300℃、圧力1.0MPa、加熱時間3分間で加熱しプレス成形して、表2に示す厚さ2.0mmの板状の熱可塑性炭素繊維複合材料(II-C)を得た。該熱可塑性炭素繊維複合材料における、熱可塑性樹脂の存在量は、試料3が炭素繊維100重量部に対し、120重量部であり、試料4が炭素繊維100重量部に対し、100重量部であった。この複合材料(II-C)の0度及び90度方向の引っ張り弾性率を測定したところ、弾性率の比(Eδ)は1.03であり、繊維配向は殆ど無く、等方性が維持された成形板を得ることができた。さらに、この成形板を500℃×1時間程度炉内にて加熱し、樹脂を除去した後、炭素繊維束(A)の割合と、平均繊維数(N)を調べたところ、上記ランダムマットの測定結果と差異は見られなかった。
ナイロン6不織布の製造
ディーエスエムジャパンエンジニアリングプラスチックス(株)製のナイロン6樹脂「ノバミッド」(登録商標)1010C2(溶融温度225℃)を原料とし、メルトブロー法によりナイロン6不織布を製造した。ここで採用したメルトブロー法は、複数個配列されたオリフィスダイから溶融ポリマーを吐出し、オリフィスダイに隣接して設備した噴射ガス口から高速ガスを噴射せしめて、吐出された溶融ポリマーを細繊維化し、次いで繊維流をコレクタであるコンベヤネット上に捕集して不織布を製造する方法である。得られたナイロン6不織布は、平均繊維径5μm、1枚当たりの平均目付け量20g/m2、平均嵩密度は0.1g/cm3、平均厚さ0.2mmであった。
長さ100mm、幅25mm、厚さ1.6mmのSPCC板(冷間圧延鋼板)の片側全面をアセトンで脱脂乾燥後、発振波長1.064μm、最大定格出力20W、ビームスポット130μmのYAGレーザー(継続波)を用いて、熱可塑性炭素繊維複合材料と接合させる側の表面全体にレーザースポット中心間隔0.08mm、深さ0.08mmの格子状の溝を形成させた。
このように加工した金属表面にナイロン6フィルム(ユニチカ(株)製「エンブレム」(登録商標)ON、25μm厚、溶融温度225℃)を2枚重ねて積層した。次いで、かかるフィルム及びSPCC板表面を電磁誘導加熱により250℃まで昇温させ、直ちに常温まで冷却した。この工程によって上記ナイロンフィルムは溶融しSPCC板表面に密着した後、固化し、SPCC表面に厚さ50μmのナイロン6層を形成した。
上記参考例1で得られた連続繊維を用いた熱可塑性炭素繊維複合材料(I)を長さ100mm、幅25mmに切り出し、表面に上記ナイロン6層を有するSPCC板とシングルラップで25mm×25mmの範囲で重ね合わせ、それを金型内に入れ金型内で温度250℃、圧力0.2MPaにて5分間加熱加圧し、上記ナイロン6層を溶融させることにより、熱可塑性炭素繊維複合材料とSPCC板との接合部材を作成した。
かかる接合部材を5枚作成し、インストロン5587万能試験機により速度1mm/分で引っ張り試験を行ったところ、接合強度の平均値は13MPaであった。
長さ100mm、幅25mm、厚さ1.6mmの590MPa級ハイテン材の片側全面に実施例1と同様にレーザー加工を施して深さ0.08mmの格子状の溝を形成させた。
その片面にナイロン6フィルム(ユニチカ(株)製「エンブレム」(登録商標)ON、25μm厚、溶融温度225℃)を20枚ずつ積層設置した後、ハイテン材を電磁誘導加熱により250℃まで昇温させ、直ちに常温まで冷却した。ナイロンフィルムは溶融、密着、固化し、ハイテン材の片面に厚さ500μmのナイロン6層を形成した。
参考例2Aで得られたランダムマットからなる熱可塑性炭素繊維複合材料(II-A)の平板を、長さ100mm、幅25mmに切り出し、これを上記ナイロン6層を有するハイテン材とシングルラップで25mm×25mmの範囲で重ね合わせ、複合材料を250℃、ハイテン材を140℃に加熱し、金型を用いて0.2MPa、1分間加熱加圧した。引き続いて、上記ラップした材料のうちハイテン材を電磁誘導加熱により250℃まで昇温させ、0.2MPa、1分間加熱加圧し、熱可塑性炭素繊維複合材料とハイテン材との接合部材を作成した。
かかる接合部材を5枚作成し、インストロン5587万能試験機により速度1mm/分で引っ張り試験を行ったところ、接合強度の平均値は10MPaであった。
実施例1と同様のレーザー加工により片面に深さ0.08mmの格子状の溝を形成させたSPCC板を、300℃で10分間熱処理を行ってから、その表面に厚さ0.05mmのナイロン6層を形成したほかは、実施例1と同様の工程で、熱可塑性炭素繊維複合材料(I)とSPCCとの接合部材を作成した。
かかる接合部材を5枚作成し、インストロン5587万能試験機により速度1mm/分で引っ張り試験を行ったところ、接合強度の平均値は12MPaであった。
SPCC板の代わりに1mm厚の5052番アルミニウム板(レーザー加工により片面に深さ0.08mmの格子状の溝を形成させたもの)を用いたほかは実施例1と同様にして、アルミニウム板表面に厚さ50μmのナイロン6層を形成した。
参考例2Aで得られたランダムマットからなる熱可塑性炭素繊維複合材料(II-A)の平板を長さ100mm、幅25mmに切り出し、これを表面に上記ナイロン6層を有するアルミニウム板とシングルラップで25mm×25mmの範囲で重ね、金型を用いて250℃、0.2MPa、5分間加熱加圧し、炭素繊維複合材料と5052アルミニウム板接合部材を作成した。
かかる接合部材を5枚作成しインストロン5587万能試験機により速度1mm/分で引っ張り試験を行ったところ、アルミニウム板部分が破壊された。アルミニウム板の破壊強度から計算すると接合強度は7.1MPa以上であることがわかった。
SPCC(冷間圧延鋼板)の片側全面に、レーザー加工を行う代わりに、サンドブラストにより平均口径100μm、深さ60μmの微細なくぼみを、接合部の金属表面積に対するくぼみの総面積が20%となるように、多数形成させた後、300℃で10分間熱処理を行ったほかは実施例1と同様にして、熱可塑性炭素繊維複合材料(I)とSPCCとの接合部材を作成した。かかる接合部材を5枚作成し、インストロン5587万能試験機により速度1mm/分で引っ張り試験を行ったところ、接合強度の平均値は12MPaであった。
1.6mm厚90mmφの円盤状SPCC材を用い、SPCC材の片面に実施例1と同様にレーザー加工による凹凸を形成し、レーザー加工を施した側にナイロン6フィルム(ユニチカ(株)製「エンブレム」(登録商標)ON、25μm厚、溶融温度225℃)を2枚設置した後、SPCC材を電磁誘導加熱により250℃まで昇温させ、直ちに常温まで冷却した。ナイロン6フィルムは溶融、密着、固化し、SPCC円盤に厚さ0.05mmのナイロン6層を形成した。
次に、図2のハットが成形できる金型を140℃に昇温し、参考例1で得られた炭素繊維複合材料(I)を250mm×270mmに切り出した平板と上記ナイロン6の層を有するSPCC円盤を300℃に加熱し、上記金型に仕込み、0.2MPa、1分間加熱加圧、図3の円盤接合ハット材を成形した。この円盤接合ハット材は、炭素繊維複合材料からなる接合ハット材の上面にSPCC円盤が強固に接合したものであった。
長さ100mm、幅25mm、厚さ1.6mmのSPCC(冷間圧延鋼板)の両表面に、実施例1と同様にレーザー加工を行って、レーザースポット中心間隔0.08mm、深さ0.08mmの格子状の溝を形成し、さらにその表面に以下のようにして有機被覆層を形成した。
この有機被覆層の形成では、両面に格子状の溝を有する上記金属板を、濃度15.0g/L、温度60℃の水酸化ナトリウム水溶液中で60秒間脱脂を行った後、水洗を60秒行い、80℃のオーブンで30分間乾燥した。次に、温度60℃、濃度30~50g/L、のリン酸水溶液(水以外の成分の90%以上がリン酸)中で300秒間浸漬し、次いで湯洗(60℃)および水洗を各60秒間行い、リン酸金属塩、水酸化物を主成分とする金属化合物皮膜を金属板両表面上に形成した。次に、濃度0.7g/Lのトリエトキシシリルプロピルアミノトリアジンチオールモノナトリウムのエタノール/水(体積比95/5)溶液に、金属化合物皮膜を有する金属板を室温で30分間浸漬した。その後オーブン内で160℃、10分間熱処理した。次に、濃度1.0g/LのN,N’-m-フェニレンジマレイミドと濃度2g/Lのジクミルパーオキシドを含むアセトン溶液に室温で10分間浸漬し、オーブン内150℃、10分間熱処理した。さらに金属板表面全体に濃度2g/Lのジクミルバーオキシドのエタノール溶液を室温で噴霧した後、風乾し、金属板の両面をトリアジンチオール誘導体薄層(厚さ0.1μm)で被覆するようにした。
次に、上記のように処理したSPCC板の両面に、それぞれナイロン6フィルム(ユニチカ(株)製「エンブレム」(登録商標)ON、25μm厚、溶融温度225℃)を2枚ずつ設置した後、SPCC板を電磁誘導加熱により250℃まで昇温させ、直ちに常温まで冷却した。ナイロン6フィルムは溶融・密着した後、固化し、SPCC表面に厚さ50μmのナイロン6樹脂層を形成した。
そして、参考例2Aで得られた炭素繊維複合材料(II-A)を長さ100mm、幅25mmに切り出し、上記ナイロン6樹脂層を有するSPCC板とシングルラップで25mm×25mmの範囲で重ね、金型を用いて250℃、0.2MPa、5分間加熱加圧し、熱可塑性炭素繊維複合材料とSPCC板との接合部材を作成した。
かかる接合部材を5枚作成し、インストロン5587万能試験機により速度1mm/分で引っ張り試験を行ったところ、接合強度の平均値は13MPaであった。
実施例7と同様にレーザー加工及びトリアジンチオール誘導体により表面処理を施した、長さ100mm、幅25mm、厚さ1.6mmのSPCC板(冷間圧延鋼板)を準備し、これを240℃まで昇温した後、該SPCCの上面に参考例3で得られたメルトブロー法によるナイロン6不織布を2枚積層した。また、炭素繊維複合材料として参考例2Bで得られた等方性ランダムマット材を用いた2種の複合材料(II-B、表1の試料1及び試料2)をそれぞれ長さ100mm、幅25mmに切り出し、80℃/5時間で乾燥処理させた。これらの複合材料を、ナイロン6不織布が複合材料とSPCC板の上記処理面と間に配置されるようシングルラップで25mm×25mmの範囲で重ね合わせ、プレス成形機にて温度240℃、圧力0.5MPaの条件で、1分間加熱加圧処理し、ナイロン6不織布を溶融させることで、厚さ400μmのナイロン6樹脂層を介して熱可塑性炭素繊維複合材料とSPCCとを接合した板状接合体を作成した。
かかる接合体をそれぞれ5枚作成し、それぞれについて実施例7と同様に引っ張り試験を行って測定した。その結果は表1に示すとおりであった。
長さ100mm、幅25mm、厚さ1.6mmのSPCC板(冷間圧延鋼板)を、実施例7と同様にして凹凸形成及びトリアジンチオール誘導体による表面処理をした後、240℃まで昇温させた。このSPCC板の上面にナイロン6フィルム(ユニチカ(株)製「エンブレム」(登録商標)ON、25μm厚)を2枚設置した。
一方、参考例2Cの方法で得られた表2に示す2種の等方性ランダムマット材を用いた炭素繊維複合材料(II-C、表2の試料3,4)を、それぞれ長さ100mm、幅25mmに切り出し、80℃/5時間で乾燥処理させ、SPCC板の上記処理面上に、ナイロン6フィルムとシングルラップで25mm×25mmの範囲で重ね、その状態で、プレス成型機にて温度240℃、圧力0.5MPaで、1分間加熱加圧処理し、ナイロン6フィルムを溶融させて熱可塑性炭素繊維複合材料とSPCCとの接合体を作成した。
かかる接合体を5枚作成し、それぞれについて実施例7と同様に引っ張り試験を行ったところ、各接合体の接合強度(5枚の平均値)は表2に示すとおりであった。
また、接合と成形とを同時にあるいは連続して同一金型内で行うこともできるので、これらを同時に又は連続的に行えば、所望形状に成形した炭素繊維複合材料と金属との接合体(金属複合成形体)を少ない工程でかつ短時間で製造することが可能となる。
本出願は、2012年3月29日出願の日本特許出願(特願2012-076865)に基づくものであり、その内容はここに参照として取り込まれる。
2.熱可塑性樹脂層
3.金属表面凹凸部
4.金属
Claims (18)
- 熱可塑性樹脂をマトリックスとする炭素繊維複合材料と金属とを接合させてなる接合部材を製造する方法であって、
接合部の金属表面に深さ0.02~0.6mmの凹凸形状を形成させる工程(i)と、
金属表面と複合材料表面の間の接合部に厚さが5μm以上5mm以下の範囲にある熱可塑性樹脂層を設ける工程(ii)と、
該接合部を加熱して該熱可塑性樹脂層を溶融させることにより金属と複合材料とを一体に結合させる工程(iii)と、
を含む接合部材の製造方法。 - 金属表面に形成される凹凸形状が、溝間隔0.02~0.6mmの格子状の溝である、請求項1記載の接合部材の製造方法。
- レーザーにより金属表面に凹凸形状を形成させる、請求項2に記載の接合部材の製造方法。
- 金属表面に形成される凹凸形状が、直径0.02~0.6mmのくぼみである、請求項1記載の接合部材の製造方法。
- ブラストにより金属表面に凹凸を形成させる、請求項4に記載の接合部材の製造方法。
- 凹凸を形成した金属表面に有機被覆層を設ける工程(i-A)を含む、請求項1記載の接合体の製造方法。
- 有機被覆層が、トリアジンチオール誘導体を含有する層である、請求項6に記載の製造方法。
- 熱可塑性樹脂層の樹脂と炭素繊維複合材料におけるマトリックス樹脂が、同種の樹脂である、請求項1に記載の接合体の製造方法。
- 熱可塑性樹脂層が、実質的に熱可塑性樹脂からなるフィルム、シート又は不織布の少なくとも1枚から形成される、請求項1に記載の接合体の製造方法。
- フィルム、シート又は不織布を実質的に構成する熱可塑性樹脂が、熱可塑性炭素繊維複合材料におけるマトリックス樹脂と同種の樹脂である、請求項9に記載の接合体の製造方法。
- 工程(ii)において、熱可塑性樹脂層を接合部となる金属表面に融着させ、これを熱可塑性樹脂層が炭素繊維複合材料の表面と接するように炭素繊維複合材料と積層する請求項1に記載の接合部材の製造方法。
- 金属が、鉄、アルミニウム及びそれらの合金より選択される少なくとも1種を含む、請求項1に記載の接合部材の製造方法。
- 金属が、少なくとも接合部に、平面又は曲面を有する部材である、請求項1に記載の接合部材の製造方法。
- 熱可塑性炭素繊維複合材料におけるマトリックスの熱可塑性樹脂の存在量が、炭素繊維100重量部に対し、50~1000重量部である、請求項1に記載の接合部材の製造方法。
- 熱可塑性炭素繊維複合材料における炭素繊維の平均繊維長が、3~100mmである、請求項14に記載の接合体の製造方法。
- 熱可塑性炭素繊維複合材料が、炭素繊維の等方性ランダムマットと熱可塑性樹脂とから構成され、上記マットにおける下記式(a)で定義される臨界単糸数以上で構成される炭素繊維束(A)のマットの繊維全量に対する割合が20Vol%以上99Vol%未満であり、かつ炭素繊維束(A)中の平均繊維数(N)が下記式(b)を満たす、請求項15に記載の接合体の製造方法。
臨界単糸数=600/D (a)
0.7×104/D2<N<1×105/D2 (b)
(ここでDは炭素繊維の平均繊維径(μm)である) - 熱可塑性樹脂をマトリックスとする炭素繊維複合材料と金属とを接合させてなる接合部材を製造する方法であって、
接合部の金属表面に深さ0.02~0.6mmの凹凸部を複数個形成させる工程と、
上記金属表面にトリアジンチオール誘導体の有機被覆層を形成させる工程と、
金属表面のトリアジンチオール誘導体の有機被覆層の上に、熱可塑性樹脂層を融着させて厚さが5μm以上5mm以下の範囲にある熱可塑性樹脂を形成する工程と、
上記熱可塑性樹脂層の上に熱可塑性炭素繊維複合材料を積層することにより金属/トリアジンチオール誘導体の有機被覆層/熱可塑性樹脂層/熱可塑性炭素繊維複合材料を含む積層体とする工程と、
得られた積層体を厚さ方向に加圧するとともに加熱して該熱可塑性樹脂層を溶融させることにより金属と複合材料とを一体に結合させる工程、
を含む、接合部材の製造方法。 - 請求項1又は請求項17の方法により得られる、熱可塑性炭素繊維複合材料と金属とが熱可塑性樹脂層を介して接合している接合部材であって、引っ張り速度1mm/秒で引っ張り試験を行ったときの接合強度が5MPa以上である接合部材。
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Also Published As
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US9527230B2 (en) | 2016-12-27 |
US20150064409A1 (en) | 2015-03-05 |
EP2832526A4 (en) | 2015-03-25 |
JPWO2013146900A1 (ja) | 2015-12-14 |
CN104245282A (zh) | 2014-12-24 |
JP5634641B2 (ja) | 2014-12-03 |
EP2832526A1 (en) | 2015-02-04 |
KR20140141583A (ko) | 2014-12-10 |
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