WO2011086984A1 - アルミニウム合金部材と樹脂部材とのレーザー接合方法 - Google Patents
アルミニウム合金部材と樹脂部材とのレーザー接合方法 Download PDFInfo
- Publication number
- WO2011086984A1 WO2011086984A1 PCT/JP2011/050238 JP2011050238W WO2011086984A1 WO 2011086984 A1 WO2011086984 A1 WO 2011086984A1 JP 2011050238 W JP2011050238 W JP 2011050238W WO 2011086984 A1 WO2011086984 A1 WO 2011086984A1
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- Prior art keywords
- aluminum alloy
- alloy member
- resin
- etching
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- Prior art date
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- 239000011347 resin Substances 0.000 title claims abstract description 55
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- 238000005304 joining Methods 0.000 title claims abstract description 23
- 238000000034 method Methods 0.000 title claims description 71
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- 239000000463 material Substances 0.000 claims description 57
- 239000000243 solution Substances 0.000 claims description 38
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- 229910018125 Al-Si Inorganic materials 0.000 claims description 17
- 229910018520 Al—Si Inorganic materials 0.000 claims description 17
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 17
- 229910052782 aluminium Inorganic materials 0.000 claims description 15
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 12
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- 239000010703 silicon Substances 0.000 claims description 12
- 239000007864 aqueous solution Substances 0.000 claims description 6
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- 238000001035 drying Methods 0.000 description 6
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- 239000003513 alkali Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
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- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
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- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
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- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
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- 150000003842 bromide salts Chemical class 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
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- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/02—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
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- B29C65/16—Laser beams
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
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- B23K26/32—Bonding taking account of the properties of the material involved
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
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- B23K26/32—Bonding taking account of the properties of the material involved
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
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- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/02—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
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- B29C66/303—Particular design of joint configurations the joint involving an anchoring effect
- B29C66/3032—Particular design of joint configurations the joint involving an anchoring effect making use of protrusions or cavities belonging to at least one of the parts to be joined
- B29C66/30325—Particular design of joint configurations the joint involving an anchoring effect making use of protrusions or cavities belonging to at least one of the parts to be joined making use of cavities belonging to at least one of the parts to be joined
- B29C66/30326—Particular design of joint configurations the joint involving an anchoring effect making use of protrusions or cavities belonging to at least one of the parts to be joined making use of cavities belonging to at least one of the parts to be joined in the form of porosity
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/73—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
- B29C66/731—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the intensive physical properties of the material of the parts to be joined
- B29C66/7316—Surface properties
- B29C66/73161—Roughness or rugosity
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/74—Joining plastics material to non-plastics material
- B29C66/742—Joining plastics material to non-plastics material to metals or their alloys
- B29C66/7422—Aluminium or alloys of aluminium
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F1/00—Etching metallic material by chemical means
- C23F1/10—Etching compositions
- C23F1/14—Aqueous compositions
- C23F1/16—Acidic compositions
- C23F1/20—Acidic compositions for etching aluminium or alloys thereof
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2791/00—Shaping characteristics in general
- B29C2791/004—Shaping under special conditions
- B29C2791/009—Using laser
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/82—Testing the joint
- B29C65/8207—Testing the joint by mechanical methods
- B29C65/8215—Tensile tests
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/01—General aspects dealing with the joint area or with the area to be joined
- B29C66/02—Preparation of the material, in the area to be joined, prior to joining or welding
- B29C66/022—Mechanical pre-treatments, e.g. reshaping
- B29C66/0224—Mechanical pre-treatments, e.g. reshaping with removal of material
- B29C66/02245—Abrading, e.g. grinding, sanding, sandblasting or scraping
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/71—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
- C09J2301/416—Additional features of adhesives in the form of films or foils characterized by the presence of essential components use of irradiation
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2400/00—Presence of inorganic and organic materials
- C09J2400/10—Presence of inorganic materials
- C09J2400/16—Metal
- C09J2400/163—Metal in the substrate
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2400/00—Presence of inorganic and organic materials
- C09J2400/10—Presence of inorganic materials
- C09J2400/16—Metal
- C09J2400/166—Metal in the pretreated surface to be joined
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2400/00—Presence of inorganic and organic materials
- C09J2400/20—Presence of organic materials
- C09J2400/22—Presence of unspecified polymer
- C09J2400/226—Presence of unspecified polymer in the substrate
Definitions
- the present invention relates to a laser bonding method that exhibits high bonding strength between an aluminum alloy member and a resin member.
- An aluminum-resin composite material obtained by integrating an aluminum member and a synthetic resin, which are different materials, is used in a wide range of fields such as automobiles, home appliances, and industrial equipment.
- an aluminum-resin composite material an aluminum member and a resin member, which are pressure-bonded with an adhesive interposed, has been used.
- a method for integrating a high-strength engineering resin without the intervention of an adhesive has been proposed.
- Patent Document 1 in a method for joining a metal material and a resin material, a laser light source is used to heat the joint to a temperature at which bubbles are generated in the resin material of the joint in a state where the metal material and the resin material are combined.
- a metal-resin joining method for joining together has been proposed.
- the above joining method is also a useful technique from the viewpoint of obtaining a composite material in which a metal material and a resin member are integrally joined.
- a composite material has a strong adhesive force (adhesion force) and rigidity. Is not enough to apply to the required mechanical structure. Therefore, there is a demand for an aluminum-resin composite in which a high strength resin member is bonded with a strong adhesive force.
- Patent Documents 2 and 3 propose a method for producing an aluminum-resin composite that meets the above-mentioned requirements.
- Patent Document 2 an aluminum alloy component whose surface is covered with a recess having a number average inner diameter of 10 to 80 nm by electron microscope observation after being immersed in one or more aqueous solutions selected from ammonia, hydrazine, and a water-soluble amine compound And a thermoplastic synthetic resin composition part having a resin composition in which the main component is a polyamide resin and the subcomponent is an impact resistance improving material, and is fixed to the surface of the aluminum alloy part by injection molding.
- This composite is intended to firmly bond a polyamide resin composition by forming the surface of an aluminum alloy part so as to be covered with ultrafine recesses or hole openings.
- Patent Document 3 in joining a thermoplastic resin material and a metal material, a thermoplastic film compatible with the thermoplastic resin material is interposed at the joining interface, and the metal material is heated by irradiating laser light.
- a joining method between a thermoplastic resin material and a metal material which is characterized by melting and welding the film. This joining method is intended to maintain high joining strength by interposing a thermoplastic film in advance at the interface between the thermoplastic resin material and the metal material to relieve the stress generated during joining.
- An object of the present invention is to provide a laser joining method between a resin member and a resin member.
- the aluminum alloy member is subjected to an etching process to form an uneven portion having unevenness on the surface, and then the aluminum alloy One surface of the member is overlapped with the resin member, and then the other surface of the aluminum alloy member is irradiated with laser light to soften the resin member in contact with the aluminum alloy member, and the uneven portion with the resin. It is characterized by filling. It is preferable to blast the aluminum alloy member prior to the etching process.
- the bonded aluminum alloy member it is preferable to use an aluminum alloy member in which a plurality of concave portions are formed due to the unevenness obtained by the etching treatment or the blast treatment and the etching treatment.
- the concave portion preferably has an opening width of 0.1 ⁇ m to 30 ⁇ m and a depth of 0.1 ⁇ m to 100 ⁇ m.
- the opening width is perpendicular to the thickness direction in the thickness direction cross section of the aluminum alloy member, and between the top line passing through the highest part of the uneven part and the bottom line passing through the deepest part. It was measured by observation with a scanning electron microscope at the half line.
- the aluminum alloy member subjected to the etching treatment or the blasting treatment and the etching treatment has a concave portion having an opening width of 0.1 ⁇ m or more and 30 ⁇ m or less having a plurality of convex portions made of eutectic silicon crystal on the inner surface. It is preferable to use an Al—Si based aluminum alloy member having a plurality of parts or the entire surface, wherein the convex part made of the eutectic silicon crystal has a sphere equivalent particle diameter of 0.1 ⁇ m or more and 10 ⁇ m or less.
- the aluminum alloy member to be bonded is made of an Al—Si based aluminum alloy member, and the protrusions made of the eutectic silicon crystal as described above due to the unevenness obtained by the etching process or the blasting process and the etching process. It is preferable to use one in which a plurality of concave portions having a portion on the inner surface are formed on a part or the entire surface of the bonded aluminum alloy member.
- the opening width is perpendicular to the thickness direction in the thickness direction cross section of the aluminum alloy member, and between the top line passing through the highest part of the uneven part and the bottom line passing through the deepest part. It was measured by observation with a scanning electron microscope at the half line.
- the convex portion made of the eutectic silicon crystal protrudes and precipitates on the inner surface of the concave portion in an amount of 0.001 g / m 2 or more and 1 g / m 2 or less, and has a convex portion of the eutectic silicon crystal. It is preferable that a plurality of concave portions having an opening width of 0.1 ⁇ m or more and 30 ⁇ m or less simultaneously exist.
- an acid aqueous solution having an acid concentration of 0.1 wt% or more and 80 wt% or less containing a halogen ion concentration within a range of 0.1 g / L or more and 300 g / L or less is used as an etching solution. It is preferable to use a solution prepared by adding a water-soluble inorganic halogen compound to an acid aqueous solution. Furthermore, as a blasting process performed before an etching process, what is implemented by an air nozzle system is preferable.
- the etching process performed before laser beam irradiation, or a blast process and an etching process are enough only from the viewpoint of obtaining the joined body with high joint strength, and the joint surface with the resin member of a to-be-joined aluminum alloy member. However, it may be the entire surface.
- an uneven shape complicated in advance is imparted to the surface of an aluminum alloy member used for manufacturing an aluminum-resin composite material. For this reason, for example, when a resin member is bonded to the surface thereof by a laser bonding method, the anchor effect is effectively exerted by the complicated uneven shape, and an aluminum-resin composite having a high bonding strength can be easily obtained.
- an Al alloy material be used as an aluminum alloy material, but an Al-Si based cast alloy can be used, so that a composite having a high degree of freedom in shape can be manufactured at low cost. become.
- the aluminum-resin composite produced in this way has extremely high adhesion strength and airtightness at the interface (aluminum / resin interface) between the aluminum alloy member and the resin molded body, and is exposed to harsh environments. Furthermore, the excellent adhesion strength and airtightness can be maintained, and high reliability can be maintained over a long period of time.
- the aluminum-resin composite having high bonding strength obtained by the method of the present invention is a metal in a wide range of fields including, for example, various sensor parts for automobiles, various switch parts for home appliances, and capacitor parts for various industrial equipment.
- -It can be suitably used for a resin-integrated molded part, and is preferably used for a metal-resin-integrated molded part requiring high bond strength.
- the inventors of the present invention have intensively studied the causes and countermeasures for not obtaining sufficient bonding strength by the method for producing an aluminum-resin composite employing the laser bonding method proposed in Patent Documents 1 and 3 above. .
- the softened resin member and the unevenness of the aluminum surface are not sufficiently engaged, and when manufacturing the aluminum-resin composite, the aluminum alloy member The improvement of surface properties was examined.
- the present invention has found that even in an Al—Si based casting alloy, an unevenness having a high anchor effect can be formed on the surface thereof by performing an effective etching treatment. Details will be described below.
- FIG. 3 shows the result of observing the surface of the sample used in Examples described later with a scanning electron microscope. It can be seen that the Si crystal protrudes into the concave portion formed between the primary crystals ⁇ -Al to form the convex portion.
- the anchor function when joining the resin member by laser light irradiation to the concave portion where the residual Si protrudes from the wall surface between the primary ⁇ -Al will be performed. It is what. In order to effectively exhibit the anchor effect, it is effective to make the concave portions to be formed fine and to make the convex portions formed by the projected Si crystal fine and large, and it is necessary to adjust the chemical etching conditions. . Preferred etching conditions will be described later.
- an Al casting alloy which is an Al—Si alloy
- a blast treatment as a pretreatment before the etching treatment.
- an air nozzle type blasting is preferable as a blasting method.
- the reason why the blast treatment is recommended before the etching treatment is as follows.
- an Al—Si-based Al casting alloy having a complicated metal structure if blasting is not performed, uneven etching may occur in some cases, making uniform etching difficult.
- rapid heating and rapid cooling are repeated on the outermost surface of the metal due to the collision of the shot media, and the surface structure is made finer and uniform. Therefore, a uniform process can be performed by performing an etching process after the blasting process.
- the air nozzle type is particularly preferable because, for example, the jetting pressure of the medium is higher than that of the shot type.
- the media is stronger than the shot type blasting with a lower jetting pressure.
- a double roughened structure effective for resin bondability can be formed by combining with an etching process.
- the size of the convex portion made of the eutectic Si crystal is 0.1 ⁇ m or more and 10 ⁇ m or less in terms of a sphere equivalent particle diameter. Is preferable. If the Si crystal size is less than 0.1 ⁇ m or less, the convex portion itself made of the eutectic Si crystal is likely to be broken and the anchor action may not be exhibited. On the other hand, even when the Si crystal size exceeds 10 ⁇ m, the size may be too large to exhibit the anchoring action.
- the concave portion from which the residual Si protrudes on the wall surface is perpendicular to the thickness direction in the cross section in the thickness direction of the aluminum alloy member, and the top line passing through the highest portion of the uneven portion and the bottom line passing through the deepest portion
- the opening width measured by observation with a scanning electron microscope is 0.1 ⁇ m or more and 30 ⁇ m or less, preferably 0.5 ⁇ m or more and 20 ⁇ m or less, more preferably 1 ⁇ m or more and 10 ⁇ m or less
- the depth from the top line to the bottom line may be from 0.1 ⁇ m to 100 ⁇ m, preferably from 0.5 ⁇ m to 50 ⁇ m.
- the opening width of the concave portion is narrower than 0.1 ⁇ m, it is difficult for the molten resin to enter during resin bonding, and a minute gap is generated at the interface between the aluminum alloy member and the resin member, resulting in excellent adhesion strength and airtightness.
- the dissolution reaction proceeds excessively during the surface treatment (etching treatment) of the aluminum molded body, so that the material surface is missing or the thickness of the material is increased. This may cause problems, resulting in a product with insufficient material strength and a decrease in productivity.
- the density of the plurality of concave portions in which the residual Si of the Al—Si-based Al alloy protrudes on the wall surface has an opening width of 0.5 ⁇ m to 20 ⁇ m and a depth of 0.5 ⁇ m to 20 ⁇ m per 0.1 mm square It is preferable that one or two or more types within the range are present in the range of about 5 or more and 200 or less.
- the surface structure of the Al-Si based aluminum alloy member was analyzed by silicon element and aluminum element analysis by mapping analysis with an energy dispersive X-ray analyzer (Horiba Seisakusho EMAX-7000), it was present in the eutectic part. It is preferable that the portion where only Si to be distributed occupies 5% or more and 80% or less. If the Si distribution site is less than 5%, an effective anchor effect may not be exhibited. On the other hand, if it exceeds 80%, the dissolution of the primary crystal ⁇ -Al that forms the wall surface of the concave portion cannot be ignored, the wall surface dissolves, and the Si crystal is deposited in the concave portion, which has an anchoring effect on the resin component. May not work.
- the protruding amount of the convex portion made of the eutectic Si crystal protrudes and precipitates on the inner surface of the concave portion in an amount of 0.001 or more and 1 g / m 2 or less. If it is less than 0.001 g / m 2 , an effective anchor effect may be difficult to be exhibited. On the other hand, when the amount exceeds 1 g / m 2 , the dissolution of primary ⁇ -Al that forms the wall surface of the concave portion cannot be ignored, and the wall surface dissolves and Si crystals are deposited in the concave portion, and anchor to the resin component. The effect may stop working.
- the protrusion amount of the convex portion is obtained by scraping the Si crystal formed on the surface of the Al—Si-based aluminum alloy member using a brush and then collecting crystal particles collected using a 0.1 ⁇ m PC membrane filter. It is measured by gravimetric method.
- the plurality of concave portions formed due to the concave and convex portions on the surface of the aluminum member are orthogonal to the thickness direction in the thickness direction cross section of the aluminum alloy member, and are the highest of the concave and convex portions. It is measured by observation with a scanning electron microscope in a half line between a top line passing through the part and a bottom line passing through the deepest part.
- the opening width is 0.1 ⁇ m or more and 30 ⁇ m or less, preferably 0.5 ⁇ m or more and 20 ⁇ m or less, more preferably 1 ⁇ m or more and 10 ⁇ m or less, and the depth from the top line to the bottom line is 0.1 ⁇ m or more and 100 ⁇ m or less.
- the size is preferably 0.5 ⁇ m or more and 50 ⁇ m or less.
- this concave portion When the opening width of this concave portion is narrower than 0.1 ⁇ m, it becomes difficult for the molten resin to enter during resin bonding, and a minute gap is generated at the interface between the aluminum alloy member and the resin molded body, thereby providing excellent adhesion strength and airtightness. On the other hand, if it is attempted to make the width larger than 30 ⁇ m, the dissolution reaction proceeds excessively during the surface treatment (etching treatment) of the aluminum molded body, and the material surface is missing or the thickness of the material is reduced. The problem of an increase arises, and a product with insufficient material strength may be generated, causing a decrease in productivity.
- the depth is shallower than 0.1 ⁇ m, it may be difficult to obtain a sufficient resin-molded portion, and conversely, if the depth is more than 30 ⁇ m, the surface treatment (etching treatment) of the aluminum molded body is difficult. ), The dissolution reaction may proceed excessively, resulting in problems such as missing material surfaces or increased material thickness reduction.
- the opening width per 0.1 mm square is 0.5 ⁇ m to 20 ⁇ m and the depth is 0.5 ⁇ m to 20 ⁇ m. It is preferable that one or two or more types within the range of 5 are present in the range of about 5 or more and 200 or less.
- the plurality of concave portions of the aluminum alloy member are concave portions having protrusions protruding from a part of the opening edge portion toward the center in the opening width direction (FIG. 5A). Or a concave portion (see FIG. 5 (b)) having a protruding portion protruding like a snow candy toward the center of the opening width direction from the entire opening edge portion.
- a concave part having a double concave part structure in which concave parts are formed see FIG. 5C
- a concave part having an internal concave-convex structure in which internal protrusions are formed on the inner wall surface (FIG. 5D).
- a concave part having a double concave part structure in which concave parts are formed see FIG. 5C
- a concave part having an internal concave-convex structure in which internal protrusions are formed on the inner wall surface (FIG. 5D).
- these double concave structure or internal uneven structure may coexist.
- a double concave portion structure or internal concave-convex structure exists, so that the concave portion of the aluminum alloy member and the insertion portion of the resin molded body are more mutually connected. It bonds firmly and exhibits better adhesion strength and airtightness between the aluminum alloy member and the resin molded body.
- an aluminum alloy material is acid such as hydrochloric acid, phosphoric acid, sulfuric acid, acetic acid, oxalic acid, ascorbic acid, benzoic acid, butyric acid, citric acid, formic acid, lactic acid, isobutyric acid, malic acid, propionic acid, tartaric acid, etc.
- the etching method include dipping in an etching solution made of a solution to form a predetermined uneven portion on the surface of the aluminum alloy material.
- Etching solutions used for this purpose include acid solutions of hydrochloric acid solution, phosphoric acid solution, dilute sulfuric acid solution, acetic acid having an acid concentration of 0.1% by weight to 80% by weight, preferably 10% by weight to 50% by weight.
- examples thereof include oxalic acid solutions having an acid concentration of 0.1% by weight to 30% by weight, preferably 10% by weight to 20% by weight.
- a halide may be added to these acid solutions for the purpose of further promoting the dissolution of the eutectic ⁇ -Al.
- the halide include chlorides such as sodium chloride, potassium chloride, magnesium chloride, and aluminum chloride, fluorides such as calcium fluoride, and bromides such as potassium bromide.
- Chloride is preferable in consideration of safety and the like, and the halogen ion concentration in the etching solution is 0.1 g / liter (g / L) to 300 g / L, preferably 1 g / L to 100 g / L. L or less is preferable.
- an acid solution having strong oxidizing power such as nitric acid or concentrated sulfuric acid having a concentration exceeding 80% by weight, sodium hydroxide, Alkaline solutions such as potassium hydroxide are not suitable.
- An acid solution having a relatively strong oxidizing power, such as concentrated sulfuric acid has a film forming ability with respect to an aluminum alloy. On the contrary, a strong oxide film is formed on the surface of the aluminum alloy member, and it becomes difficult to dissolve the oxide film.
- the processing conditions for etching the surface of the aluminum alloy member using the above etching solution should be formed on the aluminum alloy member, such as the type of etching solution used, acid concentration, halogen ion concentration, etc. It also differs depending on the number and size of the plurality of concave portions.
- the bath temperature is 20 ° C. or more and 80 ° C. or less and the immersion time is 1 minute or more and 40 minutes or less
- the bath temperature is 20 ° C. or more and 60 ° C.
- the bath temperature is 20 ° C. or more and 70 ° C. or less and the immersion time is 1 minute or more and 50 minutes or less
- the bath temperature is 20 ° C. or more and 60 ° C. or less and the immersion time is 1 minute or more and 60 minutes or less
- the bath temperature ranges from 20 ° C. to 50 ° C.
- the immersion time ranges from 1 minute to 20 minutes
- the bath temperature ranges from 20 ° C. to 80 ° C.
- the immersion time ranges from 1 minute to 30 minutes. It is good. The higher the acid concentration and bath temperature of the etching solution used, the more remarkable the effect of the etching treatment, and the shorter the treatment time becomes possible, but the bath temperature is less than 20 ° C., and the dissolution rate is slow, so the productivity is poor. In addition, when the bath temperature exceeds 80 ° C., the dissolution reaction proceeds rapidly and it becomes difficult to control. With respect to the immersion time, it is difficult to control dissolution if it is less than 1 minute, and conversely, if the immersion time exceeds 60 minutes, it causes a decrease in productivity.
- an aluminum alloy member having a concave portion is formed by etching the aluminum alloy material as described above, if necessary, the surface of the aluminum alloy material before the etching treatment is degreased, surface-adjusted, surface
- a pretreatment comprising an acid treatment with an acid solution and / or an alkali treatment with an alkali solution may be performed.
- examples of the acid solution used for this pretreatment include those prepared with commercially available acid degreasing agents, mineral acids such as sulfuric acid, nitric acid, hydrofluoric acid, and phosphoric acid, organic acids such as acetic acid and citric acid, and the like.
- acid reagents such as mixed acid obtained by mixing acid, etc. can be used, and as an alkaline solution, for example, what was prepared with a commercially available alkaline degreasing agent, caustic soda, etc.
- What was prepared with the alkali reagent, or what was prepared by mixing these things etc. can be used.
- the operation method and treatment conditions of the pretreatment performed using the acid solution and / or the alkali solution can be performed by a method such as an immersion method or a spray method.
- the aluminum alloy material that has been subjected to pretreatment or etching treatment is dried as necessary.
- This drying treatment may be natural drying that is allowed to stand at room temperature, or using an air blow, a dryer, an oven, or the like. Forced drying may be used.
- the test uses two types of aluminum alloy members: i) a JIS ADC12 alloy plate having a thickness of 2 mm, a width of 50 mm, and a length of 100 mm; and ii) an A5052 alloy plate having a thickness of 2 mm, a width of 50 mm, and a length of 100 mm.
- PBT polybutylene terephthalate
- the JIS ADC12 alloy plate was manufactured by a die casting method.
- the A5052 alloy plate is A5052-H34.
- test materials were prepared by changing the surface treatment method for each aluminum alloy member. The method for preparing the five types of test materials will be described later. And about the test material which surface-treated, the surface state was observed by the method of a postscript. The results are shown in Tables 1 and 2.
- Test materials (10 in total) treated with 5 types of methods for each of the two types of aluminum alloy members are stacked one by one on the PBT and irradiated with laser light from above the aluminum alloy test material, The aluminum alloy test material and PBT were joined. At that time, as shown in Table 3, the laser welding conditions were variously changed. And the tensile shear strength was measured about the joined body of each aluminum alloy test material and PBT. A method for measuring the tensile shear strength will be described later.
- Table 4 shows the measurement results of the tensile shear strength (N / mm) of the bonding material.
- the aluminum nozzle plate (test material 5) that was not subjected to air nozzle blasting or etching as a comparative example was not bonded to PBT under all laser welding conditions.
- the bonding strength of the air nozzle blasting material is low although it is bonded.
- the etching treatment material of the present invention has higher bonding strength than the comparative example.
- the highest joint strength was obtained by combining air nozzle blasting and etching.
- Test materials 1 to 5 having the following conditions were prepared for two types of aluminum alloy plates, the JIS ADC12 alloy plate and the A5052 alloy plate.
- Test material 1 After adjusting the surface roughness of the aluminum alloy plate to Rz: 40 ⁇ m by air nozzle blasting, 90 g / L (chloride ion concentration: 61 g / L) of aluminum chloride hexahydrate in 1.2 wt% hydrochloric acid solution
- An aluminum alloy test material 1 was obtained by performing an etching treatment of immersing in an etching solution prepared by adding a product at 40 ° C. for 1 minute and then washing with water, followed by drying with hot air at 120 ° C. for 5 minutes.
- Test material 2 After adjusting the surface roughness of the aluminum alloy plate to Rz: 40 ⁇ m by air nozzle blasting, 90 g / L (chloride ion concentration: 61 g / L) of aluminum chloride hexahydrate in 1.2 wt% hydrochloric acid solution
- the aluminum casting alloy test material 2 was obtained by immersing it in an etching solution prepared by adding a product for 4 minutes at 40 ° C. and then washing with water and drying with hot air at 120 ° C. for 5 minutes.
- Test material 3 The aluminum alloy plate was washed with water after adjusting the surface roughness to Rz: 40 ⁇ m by air nozzle blasting, and then dried with hot air at 120 ° C. for 5 minutes to obtain an aluminum alloy test material 3.
- Test material 4 In an etching solution prepared by adding 90 g / L (chloride ion concentration: 61 g / L) of aluminum chloride hexahydrate to a 1.2 wt% hydrochloric acid solution without blasting the aluminum alloy plate.
- the aluminum alloy test material 4 was obtained by performing an etching treatment of immersing in water at 40 ° C. for 4 minutes and then washing with water, followed by drying with hot air at 120 ° C. for 5 minutes.
- Test material 5 The aluminum alloy plate was washed with water without being subjected to blasting or etching, and then dried with hot air at 120 ° C. for 5 minutes to obtain an aluminum alloy test material 5.
- each aluminum alloy test material obtained from two types of aluminum alloy plates the cross section of a certain area in the cross section in the thickness direction is scanned with a scanning electron microscope (Hitachi FE-SEM, S-4500 type). The observation was performed at a magnification of 1000 times, and the measurement was performed as follows based on the obtained cross-sectional observation photograph (number of measurement visual fields: 3). First, a top line (TL) perpendicular to the thickness direction and passing through the highest portion of the uneven portion is determined in the cross section in the thickness direction of the aluminum alloy test material, and then the aluminum alloy test material is substantially the same as described above.
- TL top line
- the bottom line that is orthogonal to the thickness direction of the projection and passes through the deepest part of the concavo-convex portion is determined, and a line segment is drawn in a direction perpendicular to the bottom line (BL) from the top line (TL).
- BL bottom line
- the distance between the gaps is defined as the opening width (d) of the recessed portion (see FIG. 4), and the shape and size (opening width) of the recessed portion formed due to the uneven portion on the surface of the aluminum alloy test material are observed. did.
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Abstract
Description
しかしながら、昨今、接着剤の介在なしで高強度のエンジニアリング樹脂を一体化する方法が提案されている。例えば特許文献1では、金属材料と樹脂材料の接合方法において、レーザー光源を用いることにより、金属材料と樹脂材料を合せた状態で接合部の樹脂材料に気泡を発生させる温度まで接合部を加熱することにより接合する金属樹脂接合方法が提案されている。
そこで、樹脂部材として強度の高いものを強力な接着力で接着させたアルミ-樹脂複合体が求められている。
例えば、特許文献2,3で、前記要望をかなえたアルミ-樹脂複合体の製造方法が提案されている。
この複合体は、アルミニウム合金部品表面を超微細な凹部や孔の開口部で覆う形状にしたことにより、ポリアミド系樹脂組成を強固に接着しようとするものである。
この接合方法は、熱可塑性樹脂材料と金属材料との界面に予め熱可塑性フィルムを介在させて、接合の際に生じる応力を緩和させることにより高い接合強度を維持しようとするものである。
本発明は、このような課題を解決するために案出されたものであり、アルミニウム合金部材としてその表面形状を複雑化したものを用いることにより、樹脂部材との接合強度を高めたアルミニウム合金部材と樹脂部材とのレーザー接合方法を提供することを目的とする。
エッチング処理に先立ってアルミニウム合金部材にブラスト処理を行うことが好ましい。
前記共晶シリコン結晶からなる凸部は、前記凹状部内面に0.001g/m2以上1g/m2以下の量で突出・析出しており、かつ、前記共晶シリコン結晶の凸部を有しない開口幅が0.1μm以上30μm以下の凹状部も同時に複数存在することが好ましい。
さらに、エッチング処理前に施すブラスト処理としては、エアーノズル方式により実施されるものが好ましい。
なお、レーザー光照射の前に施すエッチング処理、又はブラスト処理とエッチング処理は、接合強度の高い接合体を得るという観点からは、被接合アルミニウム合金部材の樹脂部材との接合面のみで十分であるが、全面であってもよい。
しかも、本発明方法ではアルミニウム合金素材として、一般的なAl合金材に使用できるだけでなく、Al-Si系の鋳造合金が使用できるため、形状的に自由度の高い複合体が安価で製造できるようになる。また、このように製造されたアルミ‐樹脂複合体はアルミニウム合金部材と樹脂成形体との間の界面(アルミ/樹脂界面)の密着強度や気密性が極めて高く、かつ過酷な環境に曝されてもその優れた密着強度及び気密性を保持することができ、長期に亘って高い信頼性を維持し得るものである。
その過程で、軟化した樹脂部材とアルミニウム表面の凹凸部の噛み合いが十分でないと仮定し、アルミ‐樹脂複合体を製造する際、複合化する樹脂部材との接合性を高めるべく、アルミニウム合金部材の表面性状の改善策について検討した。
そこで、本発明は、Al-Si系鋳造用合金においても、効果的なエッチング処理を施すことにより、その表面にアンカー効果の高い凹凸を形成することができることを見出している。
以下にその詳細を説明する。
実用的に多用される亜共晶-共晶近傍組成を有するAl-Si系合金の溶湯を鋳型内で凝固させたとき、図1に見られるように、初晶α-Al(1)の間をラメラー状のAl-Si共晶部(2)が埋める形態となっている。そして、Al-Si共晶部(2)は共晶α-Al(3)と共晶Si(4)から構成される形態となる。
その結果、初晶α-Al(1)の間を埋めているラメラー状の共晶部から共晶Si(4)のみが残存することとなり、凹部となった初晶α-Alの間の空隙部(5)に残存Siが前記凹部壁に突出した形態となる(図2参照)。
図3は、後述の実施例で用いた試料の表面を走査電子顕微鏡で観察した結果を示すものである。初晶α-Alの間に形成された凹状部の内部にSi結晶が突出し、凸部を形成していることがわかる。
上記アンカー効果を有効に発現させるためには、形成される凹状部を細かく、突出したSi結晶が形作る凸部を細かくかつ多くすることが有効であり、化学エッチング条件を調整することが必要となる。好ましいエッチング条件については後記する。
本発明において、Al-Si系Al合金の残存Siが壁面に突出した複数の凹状部の密度については、0.1mm四方当り開口幅0.5μm以上20μm以下及び深さ0.5μm以上20μm以下の範囲内の1種又は2種以上の大きさのものが5個以上200個以下程度の範囲で存在するのがよい。
なお、凸部の突出量は、Al-Si系のアルミニウム合金部材の表面に形成されたSi結晶を、ブラシを使用して削り落とした後、0.1μmPCメンブランフィルターを用いて採取した結晶粒子を重量法により測定したものである。
具体的には、アルミニウム合金材を塩酸、リン酸、硫酸、酢酸、シュウ酸、アスコルビン酸、安息香酸、酪酸、クエン酸、ぎ酸、乳酸、イソブチル酸、リンゴ酸、プロビオン酸、酒石酸等の酸溶液からなるエッチング液に浸漬し、このアルミニウム合金材の表面に所定の凹凸部を形成するエッチング処理の方法が挙げられる。
この目的で用いられるエッチング液としては、酸溶液として、酸濃度0.1重量%以上80重量%以下、好ましくは10重量%以上50重量%以下の塩酸溶液、リン酸溶液、希硫酸溶液、酢酸溶液等や、酸濃度0.1重量%以上30重量%以下、好ましくは10重量%以上20重量%以下のシュウ酸溶液等を挙げることができる。
好ましくは安全性等を考慮して塩化物であり、更に、エッチング液中におけるハロゲンイオン濃度が、0.1グラム/リットル(g/L)以上300g/L以下、好ましくは1g/L以上100g/L以下のものが好ましい。0.1g/L未満だとハロゲンイオンの効果が小さいため、共晶α-Alの溶解が起こり難く、Si結晶の突出部を有する凹状部が形成されないという問題が生じることがあり、300g/Lを超えるような場合はアルミニウム成形体の表面処理(エッチング処理)時に溶解反応が急激に進行するため,共晶α-Alの選択溶解により形成される凹状部及びSi結晶の突出部の制御が困難になるという問題が生じることがある。
試験には、アルミニウム合金部材として、i)厚さ2mm,幅50mm,長さ100mmのJISADC12合金板とii)厚さ2mm,幅50mm,長さ100mmのA5052合金板の2種類を用い、樹脂部材として、厚さ10mm,幅50mm,長さ100mmのPBT(ポリブチレンテレフタラート)を用いた。JISADC12合金板はダイカスト工法で製作した。また、A5052合金板はA5052-H34である。接合強度に及ぼす表面状態の影響を調査するために、アルミニウム合金部材ごとに表面処理方法を変えて5種類の試験材を用意した。
5種類の試験材の調製方法については後記する。
そして、表面処理を施した試験材については、後記の方法でその表面状態を観察した。その結果を表1及び表2に示す。
そして、各アルミニウム合金試験材とPBTとの接合体について、引張りせん断強度を測定した。なお、引張りせん断強度の測定手法も後記する。
比較例であるエアーノズル式ブラスト処理やエッチング処理をしないアルミニウム合金板(試験材5)では、全てのレーザー溶接条件でPBTとは接合されなかった。また、エアーノズル式ブラスト処理材では接合されるものの接合強度が低い。一方、本発明のエッチング処理材は比較例に比べて高い接合強度が得られている。また、エアーノズル式ブラスト処理とエッチング処理を組み合わせることによって、最も高い接合強度が得られた。
上記JISADC12合金板とA5052合金板の2種類のアルミニウム合金板に対して、それぞれ以下の条件の試験材1~5を用意した。
(試験材1)
アルミニウム合金板を、エアーノズル式ブラスト処理により表面粗さをRz:40μmに調整した後、1.2wt%塩酸溶液中に90g/L(塩化物イオン濃度:61g/L)の塩化アルミニウム六水和物を添加して調製したエッチング液中に40℃で1分間浸漬した後に水洗するエッチング処理を施した後、120℃の熱風で5分間乾燥させ、アルミニウム合金試験材1とした。
アルミニウム合金板を、エアーノズル式ブラスト処理により表面粗さをRz:40μmに調整した後、1.2wt%塩酸溶液中に90g/L(塩化物イオン濃度:61g/L)の塩化アルミニウム六水和物を添加して調製したエッチング液中に40℃で4分間浸漬した後に水洗するエッチング処理を施した後、120℃の熱風で5分間乾燥させ、アルミニウム鋳物合金試験材2とした。
アルミニウム合金板を、エアーノズル式ブラスト処理により表面粗さをRz:40μmに調整した後に水洗し、その後、120℃の熱風で5分間乾燥させ、アルミニウム合金試験材3とした。
アルミニウム合金板を、ブラスト処理を施すことなく、そのまま1.2wt%塩酸溶液中に90g/L(塩化物イオン濃度:61g/L)の塩化アルミニウム六水和物を添加して調製したエッチング液中に40℃で4分間浸漬した後に水洗するエッチング処理を施した後、120℃の熱風で5分間乾燥させ、アルミニウム合金試験材4とした。
アルミニウム合金板を、ブラスト処理やエッチング処理を施すことなく、そのまま水洗し、その後、120℃の熱風で5分間乾燥させ、アルミニウム合金試験材5とした。
JISADC12合金板を処理して得られた各アルミニウム合金試験材の表面を、走査型電子顕微鏡(日立製FE‐SEM、S‐4500形)を用いて観察し、シリコン結晶のサイズを観察し、また、その析出量を重量法により測定した。なお、析出量は、Al合金試験片表面に形成されたシリコン結晶を、ブラシを使用し削り落とした後、採取した結晶粒子を、0.1μmPCメンブランフィルターを使用した重量法により計測した。
先ず、アルミニウム合金試験材の厚さ方向断面においてこの厚さ方向に直交し、かつ、凹凸部の最高部を通過するトップライン(TL)を決め、次に上記と概ね同様に、アルミニウム合金試験材の厚さ方向に直交し、かつ、凹凸部の最深部を通過するボトムラインを決定し、更に、トップライン(TL)からボトムライン(BL)に対して垂直方向に線分を引き、この線分の中間部を通過し、かつ、トップライン(TL)〔あるいはボトムライン(BL)〕と平行に引かれたハーフライン(HL)上のアルミニウム合金試験材とアルミニウム合金試験材との間に存在する空隙間の距離を凹状部の開口幅(d)とし(図4参照)、アルミニウム合金試験材の表面の凹凸部に起因して形成された凹状部の形状と大きさ(開口幅)を観察した。同一のアルミニウム合金試験材の2視野についても同様の観察を行い、計3視野より観察された全ての開口幅について全測定点数で除した値を平均開口幅として、測定した。一方、上記トップライン(TL)からボトムライン(BL)までの距離で定義される凹状部の深さについても同様に観察して、平均深さを測定した。更に、凹状部の密度については、EDXにより倍率1000倍で元素マッピング分析を行い、未処理の場合と比較し、アルミ元素の蛍光X線強度が低い領域を凹状部と定義し、測定されたマッピング写真について画像処理ソフト(ImageJ)を用いて凹状部の密度を測定した。
表1に示す数値は、これらの計測値を示している。
上記5種類の方法で処理した厚さ2mm,幅50mm,長さ100mmのアルミニウム合金試験材と、厚さ10mm,幅50mm,長さ100mmのPBT(ポリブチレンテレフタラート)樹脂板を、長さ方向に15mmずつ重なり合うようにセットして、アルミニウム合金試験材の上方からレーザー光を照射させて幅方向にレーザー溶接した。レーザー溶接後、幅100mmの試験片の端から30mmの位置で幅10mmに切断加工した引張試験片を3本採取し、この引張試験片について、引張試験機で引張試験を行い、得られた荷重(N)を試験片の幅で除した値を引張せん断強度とした。なお、引張速度は8×10-3m/秒とした。
Claims (7)
- 被接合アルミニウム合金部材にエッチング処理を施して表面に凹凸を有した凹凸部を形成した後、当該アルミニウム合金部材の一方の面と樹脂部材とを重ね合わせ、その後に、前記アルミニウム合金部材の他方の面にレーザー光を照射させてアルミニウム合金部材に接している樹脂部材を軟化させて当該樹脂で前記凹凸部を充填することを特徴とするアルミニウム合金部材と樹脂部材とのレーザー接合方法。
- エッチング処理に先立ってアルミニウム合金部材にブラスト処理を行う請求項1に記載のアルミニウム合金部材と樹脂部材とのレーザー接合方法。
- 被接合アルミニウム合金部材として、前記エッチング処理、又はブラスト処理とエッチング処理により得られた凹凸部に起因して複数の凹状部が形成されたアルミニウム合金部材を用い、前記凹状部は、開口幅が0.1μm以上30μm以下の大きさであると共に、深さが0.1μm以上100μm以下の大きさであって、前記開口幅は、当該アルミニウム合金部材の厚さ方向断面においてこの厚さ方向に直交し、かつ、凹凸部の最高部を通過するトップラインと最深部を通過するボトムラインとの間のハーフラインにおいて、走査型電子顕微鏡観察により測定されたものである請求項1又は2に記載のアルミニウム合金部材と樹脂部材とのレーザー接合方法。
- 被接合アルミニウム合金部材がAl-Si系アルミニウム合金部材からなり、前記エッチング処理、又はブラスト処理とエッチング処理により得られた凹凸部に起因して複数の凹状部が表面の一部又は全面に形成されており、前記凹状部は、開口幅が0.1μm以上30μm以下の大きさであって、かつ、内面に共晶シリコン結晶からなる凸部を複数有し、前記開口幅は、当該アルミニウム合金部材の厚さ方向断面においてこの厚さ方向に直交し、かつ、凹凸部の最高部を通過するトップラインと最深部を通過するボトムラインとの間のハーフラインにおいて、走査型電子顕微鏡観察により測定されたものであり、また、前記共晶シリコン結晶からなる凸部が球相当粒子径で0.1μm以上10μm以下のサイズを有する請求項1又は2に記載のアルミニウム合金部材と樹脂部材とのレーザー接合方法。
- 前記共晶シリコン結晶からなる凸部は、前記凹状部内面に0.001g/m2以上1g/m2以下の量で突出・析出しており、かつ、前記共晶シリコン結晶の凸部を有しない開口幅が0.1μm以上30μm以下の凹状部も同時に複数存在する請求項4に記載のアルミニウム合金部材と樹脂部材とのレーザー接合方法。
- 被接合アルミニウム合金部材にエッチング処理を施す際、エッチング液として、ハロゲンイオン濃度を0.1g/L以上300g/L以下の範囲内で含む酸濃度0.1重量%以上80重量%以下の酸水溶液であって、酸水溶液中に水溶性無機ハロゲン化合物を添加して調製されたものを用いる請求項1~5のいずれか1項に記載のアルミニウム合金部材と樹脂部材とのレーザー接合方法。
- エッチング処理前に施すブラスト処理が、エアーノズル方式により実施される請求項2~6のいずれか1項に記載のアルミニウム合金部材と樹脂部材とのレーザー接合方法。
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CN2011800058350A CN102712136A (zh) | 2010-01-12 | 2011-01-11 | 铝合金部件和树脂部件的激光接合方法 |
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JP2011143539A (ja) | 2011-07-28 |
CN102712136A (zh) | 2012-10-03 |
KR101512888B1 (ko) | 2015-04-16 |
KR20120115998A (ko) | 2012-10-19 |
TW201143951A (en) | 2011-12-16 |
JP5577707B2 (ja) | 2014-08-27 |
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