JP2009120877A - Magnesium alloy parts - Google Patents
Magnesium alloy parts Download PDFInfo
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- JP2009120877A JP2009120877A JP2007293690A JP2007293690A JP2009120877A JP 2009120877 A JP2009120877 A JP 2009120877A JP 2007293690 A JP2007293690 A JP 2007293690A JP 2007293690 A JP2007293690 A JP 2007293690A JP 2009120877 A JP2009120877 A JP 2009120877A
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- magnesium alloy
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- coating layer
- alloy member
- base material
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- 229910000861 Mg alloy Inorganic materials 0.000 title claims abstract description 40
- 239000000463 material Substances 0.000 claims abstract description 120
- 238000012545 processing Methods 0.000 claims abstract description 71
- 239000011247 coating layer Substances 0.000 claims abstract description 51
- 229910052751 metal Inorganic materials 0.000 claims abstract description 35
- 239000002184 metal Substances 0.000 claims abstract description 35
- 229910003460 diamond Inorganic materials 0.000 claims abstract description 10
- 239000010432 diamond Substances 0.000 claims abstract description 10
- 239000010410 layer Substances 0.000 claims description 27
- 238000005520 cutting process Methods 0.000 claims description 9
- 230000007797 corrosion Effects 0.000 claims description 8
- 238000005260 corrosion Methods 0.000 claims description 8
- 238000005530 etching Methods 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 7
- 238000003825 pressing Methods 0.000 claims description 6
- 229910003023 Mg-Al Inorganic materials 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 4
- 230000003746 surface roughness Effects 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims 1
- 239000000395 magnesium oxide Substances 0.000 claims 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 52
- 239000004033 plastic Substances 0.000 description 39
- 238000005096 rolling process Methods 0.000 description 28
- 238000010438 heat treatment Methods 0.000 description 27
- 229910045601 alloy Inorganic materials 0.000 description 19
- 239000000956 alloy Substances 0.000 description 19
- 238000011282 treatment Methods 0.000 description 15
- 238000000034 method Methods 0.000 description 14
- 239000013078 crystal Substances 0.000 description 10
- 230000007547 defect Effects 0.000 description 9
- 238000005266 casting Methods 0.000 description 7
- 238000013461 design Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000011777 magnesium Substances 0.000 description 6
- 238000005498 polishing Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000002932 luster Substances 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000009749 continuous casting Methods 0.000 description 3
- 238000005238 degreasing Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000002708 enhancing effect Effects 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 238000005204 segregation Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000005242 forging Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- 239000012756 surface treatment agent Substances 0.000 description 2
- 239000008207 working material Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229910018131 Al-Mn Inorganic materials 0.000 description 1
- 229910021364 Al-Si alloy Inorganic materials 0.000 description 1
- 229910018137 Al-Zn Inorganic materials 0.000 description 1
- 229910018461 Al—Mn Inorganic materials 0.000 description 1
- 229910018573 Al—Zn Inorganic materials 0.000 description 1
- 229910000549 Am alloy Inorganic materials 0.000 description 1
- 229910016338 Bi—Sn Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 239000006061 abrasive grain Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000005536 corrosion prevention Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000992 sputter etching Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010119 thixomolding Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Chemical Treatment Of Metals (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
Abstract
【課題】金属質感が高いマグネシウム合金部材を提供する。
【解決手段】マグネシウム合金からなる基材と、この基材の上に形成された被覆層とを具えるマグネシウム合金部材であり、上記基材は、その表面の少なくとも一部に、金属質感が得られるように、微細な凹凸加工が施された表面加工部を具え、上記被覆層は、透明である。この部材は、表面加工部を具えることで金属質感を効果的に高められる。また、この部材は、被覆層を具えることで防食性に優れると共に、被覆層が透明であることで、表面加工部による金属質感を感じ易い。上記凹凸加工は、ヘアライン加工、ダイヤカット加工などが挙げられる。
【選択図】なしA magnesium alloy member having a high metal texture is provided.
A magnesium alloy member comprising a base material made of a magnesium alloy and a coating layer formed on the base material. The base material has a metal texture on at least a part of its surface. As described above, the coating layer is transparent, and includes a surface processed portion on which fine unevenness processing is performed. By providing the surface processed portion, the metal texture can be effectively enhanced. Moreover, this member is excellent in anticorrosion property by providing a coating layer, and it is easy to feel the metal texture by a surface processed part because a coating layer is transparent. Examples of the uneven processing include hairline processing and diamond cut processing.
[Selection figure] None
Description
本発明は、マグネシウム合金からなる基材上に被覆層を具えるマグネシウム合金部材に関するものである。特に、金属質感が高いマグネシウム合金部材に関するものである。 The present invention relates to a magnesium alloy member having a coating layer on a base material made of a magnesium alloy. In particular, it relates to a magnesium alloy member having a high metal texture.
マグネシウムに種々の添加元素を含有したマグネシウム合金が、携帯電話やノートパソコンといった携帯電気機器類の筐体や自動車部品などの部材の材料に利用されてきている。マグネシウム合金は、活性な金属であるため、上記部材の表面には、防食を目的とした表面処理が施される(例えば、特許文献1,2参照)。 Magnesium alloys containing various additive elements in magnesium have been used as materials for casings of portable electrical devices such as mobile phones and notebook computers and members of automobile parts. Since the magnesium alloy is an active metal, the surface of the member is subjected to surface treatment for the purpose of corrosion prevention (see, for example, Patent Documents 1 and 2).
また、マグネシウム合金は、六方晶の結晶構造(hcp構造)を有するため常温での塑性加工性に乏しいことから、上記筐体などのマグネシウム合金部材は、ダイカスト法やチクソモールド法による鋳造材が主流である。最近、ASTM規格におけるAZ31合金からなる板材にプレス加工を施して、上記筐体を形成することが検討されている。また、特許文献3は、ASTM規格におけるAZ91合金相当の合金からなり、プレス加工性に優れる板材を提案している。 In addition, since magnesium alloys have a hexagonal crystal structure (hcp structure) and have poor plastic workability at room temperature, magnesium alloy members such as the above casings are mainly cast materials by die casting or thixomolding. It is. Recently, it has been studied to press the plate made of AZ31 alloy in the ASTM standard to form the casing. Patent Document 3 proposes a plate material made of an alloy equivalent to the AZ91 alloy in the ASTM standard and having excellent press workability.
昨今、上記筐体といったマグネシウム合金部材に対して、金属質感を高めて高級感などを増すことが要求されている。しかし、特許文献1,2は、金属光沢を損わない表面処理剤を提案しているものの、金属質感を高めることについて検討されていない。また、特許文献3も金属質感を高めることについて言及されていない。 In recent years, it has been demanded that magnesium alloy members such as the above-described housings have a higher metallic feel and a higher-class feeling. However, Patent Documents 1 and 2 propose surface treatment agents that do not impair the metallic luster, but have not been studied for enhancing the metal texture. Patent Document 3 also does not mention enhancing the metal texture.
そこで、本発明の目的は、金属質感が高いマグネシウム合金部材を提供することにある。 Accordingly, an object of the present invention is to provide a magnesium alloy member having a high metal texture.
本発明は、マグネシウム合金からなる基材表面の少なくとも一部に、金属質感を高める加工が施された表面加工部を有することで上記目的を達成する。具体的には、本発明マグネシウム合金部材は、マグネシウム合金からなる基材と、この基材の上に形成された被覆層とを具えており、上記基材は、その表面の少なくとも一部に、金属質感が得られるように、微細な凹凸加工が施された表面加工部を有する。また、上記被覆層は、透明である。 The present invention achieves the above-mentioned object by having a surface processed portion that has been processed to enhance the metallic texture on at least a part of the surface of a base material made of a magnesium alloy. Specifically, the magnesium alloy member of the present invention comprises a base material made of a magnesium alloy and a coating layer formed on the base material, and the base material is formed on at least a part of the surface thereof. In order to obtain a metal texture, it has a surface processed portion that is finely textured. Moreover, the said coating layer is transparent.
本発明マグネシウム合金部材は、上記表面加工部を具えることで、金属質感を効果的に高められる。また、本発明部材は、被覆層を具えることで、十分な防食性を有することができる。特に、この被覆層が透明であることで外部からの光が被覆層を透過して上記表面加工部で乱反射し易く、どの方向から見ても金属質感を感じ易い。従って、本発明部材は、所望の防食性を有しながら、金属質感が高く、意匠性に優れる。以下、本発明をより詳細に説明する。 The magnesium alloy member of the present invention is provided with the above-mentioned surface processed portion, so that the metal texture can be effectively enhanced. Moreover, this invention member can have sufficient corrosion resistance by providing a coating layer. In particular, since the coating layer is transparent, light from the outside is easily transmitted through the coating layer and irregularly reflected by the surface processed portion, and the metal texture is easily felt from any direction. Therefore, the member of the present invention has high metal texture and excellent design properties while having desired corrosion resistance. Hereinafter, the present invention will be described in more detail.
<基材>
《組成》
本発明部材の基材を構成するマグネシウム合金は、Mgに添加元素を含有した種々の組成のもの(残部:Mg及び不純物)が利用でき、特に限定されない。例えば、Mg-Al系、Mg-Zn系、Mg-RE(希土類元素)系、Y添加合金などが挙げられる。特に、Alを含有するMg-Al系合金は、耐食性が高く好ましい。Mg-Al系合金としては、例えば、ASTM規格におけるAZ系合金(Mg-Al-Zn系合金、Zn:0.2〜1.5質量%)、AM系合金(Mg-Al-Mn系合金、Mn:0.15〜0.5質量%)、AS系合金(Mg-Al-Si系合金、Si:0.6〜1.4質量%)、Mg-Al-RE(希土類元素)系合金、これらMg-Al系合金に更にBi,Sn,Pb,Ca,及びBeからなる群から選択される1種以上の元素を添加した合金などが挙げられる。Alの含有量は、1.0質量%以上11質量%以下が好ましく、Al量が多くなるに従って耐食性や強度といった機械的特性に優れるが、多過ぎると塑性加工性が低下し易いため、耐食性、機械的特性及び成形性を考慮すると、8質量%以上11質量%以下がより好ましい。特に、Alを8〜11質量%、Znを0.2〜1.5質量%含有するMg-Al系合金、代表的にはAZ80,AZ91が好適に利用できる。これらの合金は、微細な凹凸加工を施した後にも基材表面が変色し難く、金属光沢などの金属質感が得られ易く好ましい。
<Base material>
"composition"
The magnesium alloy constituting the base material of the member of the present invention can be used in various compositions containing Mg with an additive element (remainder: Mg and impurities), and is not particularly limited. For example, Mg-Al, Mg-Zn, Mg-RE (rare earth element), Y-added alloy and the like can be mentioned. In particular, Mg-Al alloys containing Al are preferable because of high corrosion resistance. Examples of Mg-Al alloys include AZ alloys (Mg-Al-Zn alloys, Zn: 0.2 to 1.5 mass%) and AM alloys (Mg-Al-Mn alloys, Mn: 0.15 to 0.5 mass%), AS alloys (Mg-Al-Si alloys, Si: 0.6-1.4 mass%), Mg-Al-RE (rare earth elements) alloys, Bi-Sn, Examples thereof include an alloy to which one or more elements selected from the group consisting of Pb, Ca, and Be are added. The Al content is preferably 1.0% by mass or more and 11% by mass or less, and as the Al content increases, the mechanical properties such as corrosion resistance and strength are excellent. However, if too much, the plastic workability tends to decrease, so corrosion resistance, mechanical Considering characteristics and moldability, 8% by mass or more and 11% by mass or less is more preferable. In particular, Mg-Al alloys containing 8 to 11% by mass of Al and 0.2 to 1.5% by mass of Zn, typically AZ80 and AZ91, can be suitably used. These alloys are preferable because the surface of the base material is not easily discolored even after fine unevenness processing, and a metal texture such as metallic luster is easily obtained.
《形態》
基材は、代表的には、鋳造材を圧延した圧延材、この圧延材に更に熱処理やレベラー加工、研磨加工などを施した加工材、これら圧延材や加工材に更にプレス加工や曲げ加工、鍛造加工といった塑性加工を施した塑性加工材が挙げられる。圧延やプレス加工などの塑性加工が施された基材は、結晶粒径が細かく、鋳造材よりも強度といった機械的特性に優れるだけでなく、引け巣や空隙(ポア)といった内部欠陥や表面欠陥が少なく、良好な表面性状を有する。また、圧延材は、鋳造材に比べて表面欠陥が少ないことから、被覆層の形成前に、欠陥のパテ埋め(欠陥補正)を低減できる、或いは行わなくてもよく、また、欠陥補正の不十分による不良品の発生を低減できるため、製品歩留まりの向上に寄与することができる。以下、鋳造条件及び圧延条件を説明する。
<Form>
Typically, the base material is a rolled material obtained by rolling a cast material, a processed material obtained by further subjecting the rolled material to heat treatment, leveler processing, polishing, etc., and further pressing or bending the rolled material or processed material. Examples thereof include a plastic processed material subjected to plastic processing such as forging. Substrates subjected to plastic working such as rolling and pressing have fine crystal grain size and excellent mechanical properties such as strength than cast materials, as well as internal and surface defects such as shrinkage and voids (pores) And has good surface properties. In addition, since the rolled material has fewer surface defects than the cast material, it is possible to reduce or eliminate the defect putty (defect correction) before forming the coating layer. Since the occurrence of defective products due to sufficient can be reduced, it can contribute to the improvement of product yield. Hereinafter, casting conditions and rolling conditions will be described.
《製造方法》
[鋳造条件]
鋳造材は、双ロール法といった連続鋳造法、特に、WO/2006/003899に記載の鋳造方法で製造することが好ましい。連続鋳造法は、急冷凝固が可能であるため、酸化物や偏析などを低減でき、圧延といった塑性加工性に優れる鋳造材が得られる。また、この鋳造材に圧延を施すことで、その後のプレス加工などの塑性加工に悪影響を及ぼすような欠陥、例えば、粒径10μm以上といった粗大な晶析出物を消滅させられる。特に、AZ系合金では、Al量が多くなるほど晶析出物が生成され易い傾向にあるが、上記連続鋳造材に圧延を施すことで、合金組成にかかわらず上記欠陥が少ない圧延材が得られる。得られた鋳造材には、組成を均質化するための熱処理(溶体化処理、加熱温度:380〜420℃、加熱時間:60〜600分)や時効処理などを施してもよい。特に、AZ系合金の場合、Alの含有量が高いものは長時間溶体化を行うことが好ましい。鋳造材の大きさは特に問わないが、厚過ぎると偏析が生じ易いため、10mm以下が好ましい。
"Production method"
[Casting conditions]
The cast material is preferably produced by a continuous casting method such as a twin roll method, in particular, a casting method described in WO / 2006/003899. Since the continuous casting method can be rapidly solidified, oxides and segregation can be reduced, and a cast material excellent in plastic workability such as rolling can be obtained. Further, by rolling the cast material, defects that adversely affect plastic processing such as subsequent press processing, for example, coarse crystal precipitates having a particle size of 10 μm or more can be eliminated. In particular, AZ-based alloys tend to generate crystal precipitates as the amount of Al increases, but rolling the above continuous cast material provides a rolled material with few defects regardless of the alloy composition. The obtained cast material may be subjected to heat treatment (solution treatment, heating temperature: 380 to 420 ° C., heating time: 60 to 600 minutes) or an aging treatment for homogenizing the composition. In particular, in the case of an AZ-based alloy, it is preferable to perform solution treatment for a long time when the content of Al is high. The size of the cast material is not particularly limited, but is preferably 10 mm or less because segregation is likely to occur if it is too thick.
[圧延条件]
圧延は、加工対象の加熱温度を200〜400℃、圧延ロールの加熱温度を150〜250℃、1パスあたりの圧下率を10〜50%の条件で複数パス行うことが好ましい。また、所望の厚さの圧延材が得られるように、上記各条件を適宜組み合わせることが好ましい。上記各温度、及び1パスあたりの圧下率、パス数の条件を適宜組み合わせることで、例えば、圧延前の板厚が3〜8mmの加工対象を1mm以下、具体的には0.2mmの厚さまで圧延することが可能である。公知の条件、例えば、特許文献3に開示される制御圧延などを利用してもよい。
[Rolling conditions]
Rolling is preferably performed in a plurality of passes under the conditions that the heating temperature of the object to be processed is 200 to 400 ° C., the heating temperature of the rolling roll is 150 to 250 ° C., and the rolling reduction per pass is 10 to 50%. Moreover, it is preferable to appropriately combine the above conditions so that a rolled material having a desired thickness can be obtained. By appropriately combining the above temperatures, the reduction ratio per pass, and the number of passes, for example, a workpiece having a thickness of 3 to 8 mm before rolling is rolled to a thickness of 1 mm or less, specifically 0.2 mm. Is possible. Known conditions such as controlled rolling disclosed in Patent Document 3 may be used.
圧延加工途中に中間熱処理(加熱温度:250〜350℃、加熱時間:20〜60分)を行って、この熱処理までの加工により加工対象に導入された歪みや残留応力、集合組織などを除去、軽減すると、その後の圧延で不用意な割れや歪み、変形を防止して、より円滑に圧延できて好ましい。また、最終の圧延後に最終熱処理を施すと、強度に優れる圧延材が得られて好ましい。最終熱処理前の圧延材は、加工歪みを十分に蓄積した結晶組織を有しており、最終熱処理により微細な再結晶組織となることで強度を向上できる。また、このような再結晶組織を有する最終熱処理後の圧延材は、プレス加工時の加熱により、結晶粒が粗大化し難い。最終熱処理の加熱温度は、例えば、AZ系合金の場合、Al量が高いほど、温度を高めることが好ましく、Al量が8〜11質量%の場合、300〜340℃、加熱時間:10〜30分が好ましい。これらの熱処理において、温度が高過ぎたり、時間が長過ぎると、結晶粒が粗大化し過ぎて、プレス加工などの塑性加工性を低下させる。 Intermediate heat treatment (heating temperature: 250 to 350 ° C, heating time: 20 to 60 minutes) is performed during the rolling process to remove strain, residual stress, texture, etc. If it reduces, it is preferable that a subsequent rolling can prevent inadvertent cracking, distortion and deformation, and can be rolled more smoothly. Moreover, it is preferable to apply a final heat treatment after the final rolling because a rolled material having excellent strength can be obtained. The rolled material before the final heat treatment has a crystal structure in which processing strain is sufficiently accumulated, and the strength can be improved by forming a fine recrystallized structure by the final heat treatment. In addition, the rolled material after the final heat treatment having such a recrystallized structure is difficult to coarsen crystal grains due to heating during press working. For example, in the case of an AZ-based alloy, the heating temperature of the final heat treatment is preferably increased as the Al amount is higher. When the Al amount is 8 to 11% by mass, 300 to 340 ° C., heating time: 10 to 30 Minutes are preferred. In these heat treatments, if the temperature is too high or the time is too long, the crystal grains become too coarse and the plastic workability such as press working is lowered.
上記圧延が施された圧延材は、結晶粒径のばらつきが小さく、鋳造時の偏析(例えば、Mg17Al12といった金属間化合物)や内部欠陥、表面欠陥などが少ないことから、高い塑性加工性を有し、加工中の亀裂や割れの発生が効果的に低減され、優れた表面性状を有する。 Rolled material subjected to the above rolling has a small variation in crystal grain size, and since there are few segregations during casting (for example, intermetallic compounds such as Mg 17 Al 12 ), internal defects, surface defects, etc., high plastic workability The occurrence of cracks and cracks during processing is effectively reduced, and the surface properties are excellent.
[圧延後塑性加工前の予備加工]
得られた圧延材には、圧延材のうねりや結晶粒の配向などを矯正するためのレベラー加工や圧延材の表面を平滑化するための研磨加工を施すことが好ましい。レベラー加工は、例えば圧延材をローラーレベラーに通すことで行い、研磨加工は、湿式ベルト式研磨が代表的である。砥粒は♯240以上が好ましく、更に♯320以上、特に♯600が好ましい。上記予備加工が施された圧延材や、この圧延材にプレス加工といった塑性加工を施した塑性加工材は、後述の凹凸加工を均一的に施し易い。
[Preliminary machining after rolling and before plastic working]
The obtained rolled material is preferably subjected to leveler processing for correcting waviness of the rolled material, crystal grain orientation, and the like and polishing for smoothing the surface of the rolled material. The leveler processing is performed, for example, by passing the rolled material through a roller leveler, and the polishing processing is typically wet belt type polishing. The abrasive grains are preferably # 240 or more, more preferably # 320 or more, particularly # 600. The rolled material subjected to the preliminary processing and the plastic processed material obtained by performing plastic processing such as press processing on the rolled material are easily subjected to uneven processing described later.
[塑性加工]
プレス加工、深絞り加工、鍛造加工、ブロー加工、曲げ加工といった塑性加工は、圧延材の組織が再結晶化して、圧延材の機械的特性が大きく変化しないような温度範囲、具体的には250℃以下の温度、特に200〜250℃の温間で行うことが好ましい。このような温度の圧延材に塑性加工を行うと、塑性変形していない箇所の結晶粒の大きさがほとんど変化しないため、この箇所の強度は、塑性加工の前後で変化し難く、高強度を維持することができ、高強度な塑性加工材が得られる。
[Plastic processing]
Plastic processing such as pressing, deep drawing, forging, blow, and bending is a temperature range where the mechanical properties of the rolled material do not change significantly due to recrystallization of the rolled material, specifically 250 It is preferable to carry out at a temperature of not higher than ° C., particularly 200 to 250 ° C. When plastic working is performed on a rolled material at such a temperature, the size of the crystal grain in the portion that is not plastically deformed hardly changes, so the strength of this portion hardly changes before and after the plastic working, and high strength is achieved. It is possible to maintain a high-strength plastic working material.
上記塑性加工は、後述する凹凸加工の加工前、同凹凸加工の加工後、後述する被覆層形成前、同形成後のいずれの段階で行ってもよい。 The plastic working may be performed at any stage before or after the uneven process described later, after the uneven process, before the formation of the coating layer described later, or after the formation.
塑性加工後に熱処理を施して、塑性加工により導入された歪みや残留応力の除去、機械的特性の向上を図ってもよい。熱処理条件は、加熱温度:100〜450℃、加熱時間:5分〜40時間程度が挙げられる。 A heat treatment may be performed after the plastic working to remove strain and residual stress introduced by the plastic working and to improve the mechanical characteristics. Examples of the heat treatment conditions include a heating temperature: 100 to 450 ° C. and a heating time: about 5 minutes to 40 hours.
《表面加工部》
本発明部材は、上記基材表面の少なくとも一部に、微細な凹凸加工が施された表面加工部を具えることを特徴の一つとする。この凹凸加工は、金属質感を高めることに寄与する加工であり、具体的には、切削加工、研削加工、吹き付け加工及び酸を用いた腐食加工の少なくとも1種が挙げられる。より具体的には、ヘアライン加工、ダイヤカット加工、スピンカット加工、ショットブラスト加工、及びエッチング加工の少なくとも1種が挙げられる。本発明部材は、これらの加工のうち1種でもよいし、複数種を組み合わせた凹凸加工が施されていてもよい。
<Surface processed part>
One feature of the member of the present invention is that at least a part of the surface of the substrate is provided with a surface processed portion on which fine unevenness is applied. This concavo-convex processing is processing that contributes to enhancing the metal texture, and specifically includes at least one of cutting processing, grinding processing, spraying processing, and corrosion processing using an acid. More specifically, at least one of hairline processing, diamond cut processing, spin cut processing, shot blast processing, and etching processing may be mentioned. The member of the present invention may be one type of these processes, or may be subjected to uneven processing combining a plurality of types.
微細な凹凸とは、具体的には、表面粗さがRmax(最大高さ:最低位置から最高位置までの距離)で1μm以上200μm以下のものが挙げられる。上記範囲を満たす凹凸を有すると、本発明部材に向けられた外部からの光が本発明部材の表面で乱反射することで、本発明部材をどの方向から見ても金属質感を十分に感じることができる。1μm未満の比較的平滑な状態では、実質的に鏡面加工が施された状態と同様に優れた金属光沢が得られるものの、金属質感を高め難く、200μm超の荒れた状態では、金属質感が得られ難い。表面粗さがRmaxで1μm以上50μm以下がより好ましい。なお、基材と被覆層との密着性を高めるために基材を粗面化することがあるが、この粗面化は、金属光沢を損なわない程度に行われるものであり、金属質感が高められないと考えられる。 Specifically, the fine irregularities include those having a surface roughness Rmax (maximum height: distance from the lowest position to the highest position) of 1 μm or more and 200 μm or less. When the unevenness satisfying the above range is provided, the light from the outside directed to the member of the present invention is irregularly reflected on the surface of the member of the present invention, so that the metal texture can be sufficiently felt from any direction. it can. In a relatively smooth state of less than 1 μm, an excellent metallic luster can be obtained in the same way as in a mirror-finished state, but it is difficult to improve the metal texture, and in a rough state exceeding 200 μm, a metal texture is obtained It's hard to be done. The surface roughness is more preferably 1 μm or more and 50 μm or less in terms of Rmax. Note that the base material may be roughened to improve the adhesion between the base material and the coating layer, but this roughening is performed to the extent that the metallic luster is not impaired, and the metal texture is enhanced. It is considered impossible.
上記表面加工部は、基材表面の一部のみでもよいし、本発明部材に表裏がある場合、表側(片面側全面)だけでもよいし、全体(表裏全面)に及んでいてもよい。但し、凹凸加工後に上記塑性加工を行うと、塑性加工により凹凸が潰されて金属質感が低下する恐れがあるときには、凹凸加工を上記塑性加工後に行うことが好ましい。特に表面加工部が片面或いは表裏全面に及ぶ場合、塑性加工により凹凸が潰される可能性が高まるため、凹凸加工を上記塑性加工後に行うことが好ましい。或いは、上記塑性加工時の潤滑剤などを工夫し、表面加工部の凹凸が潰れないように塑性加工を行う場合、凹凸加工後に塑性加工を行うこともできる。例えば、凹凸加工が施された素材を、テフロン(登録商標)といったフッ素樹脂製シートに挟んでプレス加工などを行うことが挙げられる。このような塑性加工を行うと、塑性加工後に得られる部材の表面形状は、塑性加工前の素材の表面形状をほぼそのまま維持できる。従って、例えば、素材として、その全面に凹凸加工が施されたものを用いることで、基材全面が表面加工部である部材を容易に製造できる。 The surface-treated portion may be only a part of the surface of the base material, or when the member of the present invention has front and back surfaces, only the front side (the entire surface on one side) or the entire surface (the entire surface). However, when the plastic processing is performed after the uneven processing, the uneven processing is preferably performed after the plastic processing when the unevenness is crushed by the plastic processing and the metal texture may be lowered. In particular, when the surface processed portion extends over one side or the entire front and back surfaces, the possibility of crushing irregularities due to plastic processing increases, and therefore it is preferable to perform the irregular processing after the plastic processing. Alternatively, when the plastic working is performed so that the unevenness of the surface processed portion is not crushed by devising the lubricant during the plastic working, the plastic working can also be performed after the uneven processing. For example, a material that has been subjected to uneven processing is sandwiched between fluororesin sheets such as Teflon (registered trademark), and press processing is performed. When such plastic working is performed, the surface shape of the member obtained after the plastic working can maintain the surface shape of the material before the plastic working substantially as it is. Therefore, for example, a member whose entire surface of the base material is a surface processed portion can be easily manufactured by using a material whose entire surface is subjected to uneven processing as a material.
<被覆層>
本発明部材は、その表面に透明な被覆層を具えることを特徴の一つとする。透明な被覆層を基材上に具えることで、基材表面に設けられた表面加工部を目視にて確認し易く、金属質感を感じ易い。被覆層は、有色透明でもよいが無色透明であると、基材の地金自体の色合いや風合いをも感じられ、金属質感をより感じ易いと考えられる。なお、透明とは、基材が目視にて確認できる程度を言う。
<Coating layer>
One feature of the member of the present invention is that it has a transparent coating layer on its surface. By providing the transparent coating layer on the base material, it is easy to visually confirm the surface processed portion provided on the base material surface, and it is easy to feel the metal texture. The coating layer may be colored and transparent, but if it is colorless and transparent, the color and texture of the base metal itself of the base material can be felt, and the metal texture is more likely to be felt. In addition, transparent means the grade which can confirm a base material visually.
被覆層は、少なくとも防食性を有することが好ましく、更に装飾性を具えると商品価値を高められて好ましい。例えば、被覆層は、防食性を有する防食層と、保護や装飾などに機能する塗装層とを具える多層構造とすることが挙げられる。防食層は、基材側に、塗装層は、防食層の上に配する。 The coating layer preferably has at least anticorrosion properties, and further has a decorative property, which is preferable because the commercial value can be increased. For example, the coating layer may have a multilayer structure including an anticorrosion layer having anticorrosion properties and a coating layer that functions for protection and decoration. The anticorrosion layer is disposed on the substrate side, and the coating layer is disposed on the anticorrosion layer.
上記防食層は、所望の防食性を有するものであれば特に問わない。代表的には、防食処理(化成処理又は陽極酸化処理)により形成されたものが挙げられる。上記防食処理を行うと、基材表面のマグネシウムが酸化して、マグネシウムの酸化物が生成され、この酸化物からなる層が防食層として機能する。この防食層は、プレス加工といった塑性加工前に形成してもよいし、塑性加工後に形成してもよい。塑性加工前に防食層を具えると、塑性加工時にこの層が潤滑剤として機能する傾向がある。更に、この防食層は、微細なクラック(ひび)が生じた状態であるため、クラックに塗装層の構成材料が入り込むことで、塗装層との密着性が高く好ましい。 The anticorrosion layer is not particularly limited as long as it has a desired anticorrosion property. Typically, those formed by anticorrosion treatment (chemical conversion treatment or anodizing treatment) can be mentioned. When the anticorrosion treatment is performed, magnesium on the surface of the substrate is oxidized to produce an oxide of magnesium, and a layer made of this oxide functions as an anticorrosion layer. This anticorrosion layer may be formed before plastic working such as press working or after plastic working. If an anticorrosion layer is provided before plastic processing, this layer tends to function as a lubricant during plastic processing. Furthermore, since this anticorrosion layer is in a state in which fine cracks (cracks) have occurred, it is preferable because the constituent material of the coating layer enters the crack, and thus the adhesion to the coating layer is high.
上記防食層は、表面抵抗率が小さいと、具体的には、0.2Ω・cm以下であると、本発明部材が電子機器筐体である場合、接地をとることができて好ましい。表面抵抗率を小さくするには、例えば、被覆層の厚さを薄くすることが挙げられる。防食層の厚さが2μm以下であると、低抵抗の層になり易い。また、上記防食層は、厚さを2μm以下、特に0.5μm以下と薄くすると、透明感が得られ易い。なお、上記筐体などにおいて接地をとる面(筐体の裏面であることが多い)は、装飾性が求められないことが多いため、塗装層を設けず防食層のみとしてもよい。防食層のみとする箇所(例えば、表面抵抗が低いことが望まれる箇所)には、適宜マスキングなどを行って所望の箇所にのみ塗装層を形成するとよい。 It is preferable that the anticorrosion layer has a small surface resistivity, specifically, 0.2 Ω · cm or less, since it can be grounded when the member of the present invention is an electronic device casing. In order to reduce the surface resistivity, for example, the thickness of the coating layer can be reduced. When the thickness of the anticorrosion layer is 2 μm or less, it tends to be a low resistance layer. Further, when the anticorrosion layer has a thickness of 2 μm or less, particularly 0.5 μm or less, a transparent feeling can be easily obtained. Note that a surface to be grounded in the housing or the like (which is often the back surface of the housing) is often not required to have a decorative property, and thus a coating layer may not be provided and only the anticorrosion layer may be provided. It is good to form a coating layer only in a desired part by performing masking etc. suitably in the part (for example, a part where it is desired that surface resistance is low) to make only an anticorrosion layer.
また、防食層は、特許文献1に記載されるような透明な表面処理剤を用いて形成することができる。 The anticorrosion layer can be formed using a transparent surface treatment agent as described in Patent Document 1.
上記塗装層は、透明であり、かつ防食層との密着性に優れ、ある程度耐食性や表面硬度に優れるものであれば特に問わない。例えば、透明のアクリル樹脂などの樹脂を用いた公知のクリア塗装や透明のフッ素樹脂を利用することができる。上記樹脂などを利用して塗装層を形成するには、湿式法(浸漬法、スプレー塗装、電着塗装など)、乾式(PVD法、CVD法)のいずれを利用してもよい。本発明部材は、このような透明な塗装層を具えることで、金属質感を高められると共に、商品価値をも高められる。塗装層は、塑性加工により損傷する恐れがある場合、塑性加工後に形成することが好ましい。また、塗装層は、表面加工部における金属質感の良好な表出性や製造のし易さなどを考慮すると、厚さが30μm以下であることが好ましい。塗装層の厚さが厚くなると、外部からの光の反射光が干渉し合い、表面加工部のシャープさがぼやけて金属質感が薄くなる恐れがある。 The coating layer is not particularly limited as long as it is transparent, has excellent adhesion to the anticorrosion layer, and is excellent in corrosion resistance and surface hardness to some extent. For example, a known clear coating using a resin such as a transparent acrylic resin or a transparent fluororesin can be used. In order to form a coating layer using the above resin or the like, either a wet method (dipping method, spray coating, electrodeposition coating, etc.) or a dry method (PVD method, CVD method) may be used. By providing such a transparent coating layer, the member of the present invention can enhance the metal texture and the commercial value. The coating layer is preferably formed after plastic processing when there is a risk of damage due to plastic processing. In addition, the coating layer preferably has a thickness of 30 μm or less in consideration of good expression of the metal texture in the surface processed portion and ease of manufacture. When the thickness of the coating layer is increased, the reflected light from the outside interferes with each other, and the sharpness of the surface processed portion may be blurred, resulting in a thin metal texture.
本発明マグネシウム合金部材は、金属質感が高く、商品価値を高められる。 The magnesium alloy member of the present invention has a high metal texture and can increase commercial value.
以下、本発明の実施の形態を説明する。
[試験例1]
マグネシウム合金からなる基材と、その表面を被覆する被覆層とを具えるプレス成形体を作製し、外観についてパネル試験を行った。
Embodiments of the present invention will be described below.
[Test Example 1]
A press-molded body comprising a base material made of a magnesium alloy and a coating layer covering the surface thereof was produced, and a panel test was performed on the appearance.
基材は、以下のように作製する。Mg-9.0%Al-1.0%Zn(全て質量%)の組成(AZ91合金相当の組成)を有する双ロール連続鋳造法により得られた厚さ5.0mmの圧延板を用意する。鋳造はWO/2006/003899に記載の条件で行う。圧延は、加工対象(圧延対象)の加熱温度を200〜400℃、圧延ロールの加熱温度150〜250℃、1パスあたりの圧下率を10〜50%の条件で複数パス行い、厚さが0.5mmの圧延板を作製する。得られた圧延材にレベラー加工、研磨加工を順に施し、所望の大きさに切断した切断片に温間プレス加工を施して、箱状のプレス材を得る。プレス加工は直方体状の凹部を有するダイに、この凹部を覆うように上記切断片を配置して、直方体状のパンチを押し付けることで行う。パンチは60×90mmの直方体状で、切断片に当接する四つ角は所定の丸みを有する。また、上記ダイ及びパンチにはヒーターと熱電対が埋め込まれており、プレス時の温度を所望の温度に調節可能な構成としている。ここでは、200〜300℃に加熱している。 A base material is produced as follows. A rolled sheet having a thickness of 5.0 mm obtained by a twin roll continuous casting method having a composition of Mg-9.0% Al-1.0% Zn (all by mass%) (composition equivalent to AZ91 alloy) is prepared. Casting is performed under the conditions described in WO / 2006/003899. Rolling is performed in multiple passes under the conditions of a processing object (rolling object) heating temperature of 200 to 400 ° C., a rolling roll heating temperature of 150 to 250 ° C., and a rolling reduction per pass of 10 to 50%, and a thickness of 0.5 Prepare a rolled sheet of mm. The obtained rolled material is subjected to leveler processing and polishing processing in this order, and a hot press processing is performed on a cut piece cut into a desired size to obtain a box-shaped press material. The press working is performed by placing the cut piece on a die having a rectangular parallelepiped concave portion so as to cover the concave portion and pressing a rectangular parallelepiped punch. The punch has a rectangular parallelepiped shape of 60 × 90 mm, and the four corners contacting the cut piece have a predetermined roundness. In addition, a heater and a thermocouple are embedded in the die and punch, and the temperature during pressing can be adjusted to a desired temperature. Here, it is heated to 200 to 300 ° C.
なお、圧延途中に中間熱処理を施したり、圧延後に最終熱処理を施して、熱処理前までの圧延により導入された歪みなどを除去してもよい。また、鋳造材に溶体化処理を行ってから圧延を施してもよい。 In addition, an intermediate heat treatment may be performed during rolling, or a final heat treatment may be performed after rolling to remove distortion introduced by rolling before the heat treatment. Alternatively, the cast material may be subjected to a solution treatment before rolling.
(試験材1-A)
得られた箱状のプレス材において、突出した側の表面全面(約60×90mm)に、加工半径:50mm、深さ:0.02mm(20μm)、ピッチ:0.05mmのダイヤカット加工を施す。この加工は、市販のダイヤカット加工機で行う。この工程により、突出した側の表面全面がダイヤカット加工による表面加工部である基材(プレス材(塑性加工材))が得られる。
(Test Material 1-A)
The obtained box-shaped press material is subjected to diamond cutting with a processing radius of 50 mm, a depth of 0.02 mm (20 μm), and a pitch of 0.05 mm on the entire surface on the protruding side (about 60 × 90 mm). This processing is performed with a commercially available diamond cutting machine. By this step, a base material (press material (plastic working material)) in which the entire surface on the protruding side is a surface processed portion by diamond cutting is obtained.
上記基材に、下地処理を行って多層の被覆層(防食層、塗装層)を形成して、表面加工部を有する基材と被覆層とを具えるマグネシウム合金部材が得られる。下地処理は、脱脂→酸エッチング→脱スマット→表面調整という手順で行う。その後、化成処理→乾燥を行い、防食層(厚さ:約0.5μm)を形成する。脱脂から乾燥までの各工程間には水洗いを行う。塗装層(厚さ:約20μm)の形成は、スプレー塗布→焼付けという手順で行う。塗装層は、基材の外表面側(箱の外側)のみ形成し、内表面側(箱の内側)には形成していない。そのため、内表面側には、塗装層形成前にマスキングを行う。以下、各工程を詳しく説明する(各溶液の濃度は質量%を示す)。この工程により得られたものを試験材1-Aとする。なお、基材表面に欠陥があった場合、適宜パテ埋めと研磨とを行ってもよい。 The base material is subjected to a base treatment to form a multi-layer coating layer (anticorrosion layer, coating layer) to obtain a magnesium alloy member having a base material having a surface processed portion and the coating layer. The base treatment is performed in the order of degreasing → acid etching → desmutting → surface adjustment. Thereafter, chemical conversion treatment → drying is performed to form an anticorrosion layer (thickness: about 0.5 μm). Wash with water between each step from degreasing to drying. The coating layer (thickness: about 20 μm) is formed by the procedure of spray application → baking. The coating layer is formed only on the outer surface side (outside of the box) of the base material, and is not formed on the inner surface side (inside of the box). Therefore, masking is performed on the inner surface side before forming the coating layer. Hereinafter, each step will be described in detail (the concentration of each solution indicates mass%). The material obtained by this step is designated as test material 1-A. In addition, when there is a defect on the substrate surface, putty filling and polishing may be appropriately performed.
脱脂:10%KOHとノニオン系界面活性剤0.2%溶液の攪拌下、60℃、10分
酸エッチング:5%有機リン酸溶液の攪拌下、40℃、1分
脱スマット:10%KOH溶液の超音波攪拌下、60℃、5分
表面調整:pH8に調整した炭酸水溶液の攪拌下、60℃×5分
化成処理:10%リン酸を主成分とするA社製P系処理液+1%KOHを処理液として使用し、攪拌下、30℃、2分
乾燥:150℃、5分
スプレー塗布:無色透明なアクリル系塗料をスプレー塗布
焼付け:150℃、10分
Degreasing: 10% KOH and nonionic surfactant 0.2% solution under stirring, 60 ° C, 10 minutes Acid etching: 5% organic phosphoric acid solution stirring, 40 ° C, 1 minute Desmutting: Over 10% KOH solution Under sonic stirring, 60 ° C., 5 minutes Surface adjustment: 60 ° C. × 5 minutes under stirring with aqueous carbonate solution adjusted to pH 8 Chemical conversion treatment: P-type treatment solution manufactured by A company with 10% phosphoric acid as the main component + 1% KOH Used as a treatment liquid, with stirring, 30 ° C, 2 minutes Drying: 150 ° C, 5 minutes Spray coating: Spray application of colorless and transparent acrylic paint Baking: 150 ° C, 10 minutes
(試験材1-B)
得られた箱状のプレス材に上記ダイヤカット加工を行わない以外の点は、同様にして基材及び被覆層を形成した試料を試験材1-Bとする。
(Test Material 1-B)
A sample in which the base material and the coating layer are formed in the same manner except that the above-described box-shaped press material is not subjected to the diamond cutting process is referred to as test material 1-B.
得られた試験材1-A,1-Bについて、任意の10人を対象としてパネルテストを実施したところ、10人中9人が試験材1-Aの方が金属質感が高く、意匠性に優れるという回答が得られた。この結果から、基材の表面にダイヤカット加工が施された表面加工部を有し、透明な被覆層を具えるマグネシウム合金部材は、金属質感が高められていることがわかる。なお、パネルテストの対象は、パソコンや携帯電話などのマグネシウム合金部材を用いる製品のターゲット層(例えば、20歳代パソコン好きのグループなど)に応じて選ぶこともできる。以下の試験例についても同様である。 For the test materials 1-A and 1-B obtained, a panel test was conducted on any 10 people, and 9 out of 10 test materials 1-A had a higher metal texture and improved design. The answer was excellent. From this result, it can be seen that the metal texture of the magnesium alloy member having a surface processed portion subjected to diamond cutting on the surface of the base material and having a transparent coating layer is enhanced. The panel test target can also be selected according to the target layer of a product using a magnesium alloy member such as a personal computer or a mobile phone (for example, a group that likes PCs in their 20s). The same applies to the following test examples.
[試験例2]
試験例1の試験材1-Aのダイヤカット加工をヘアライン加工に変更した以外の点は、試験材1-Aと同様に作製した試料を試験材2-Aとし、外観についてパネル試験を行った。
[Test Example 2]
Except for changing the diamond-cut processing of test material 1-A in Test Example 1 to hairline processing, a sample prepared in the same manner as test material 1-A was used as test material 2-A, and a panel test was performed on the appearance. .
この試験では、表面粗さがRmax(最大高さ)で10μmであるヘアライン加工を行った。得られた試験材2-Aと、試験例1で作製した試験材1-B(ヘアライン加工やダイヤカット加工を施していないもの)とについて、任意の10人を対象としてパネルテストを実施したところ、10人中8人が試験材2-Aの方が金属質感が高く、意匠性に優れるという回答が得られた。この結果から、基材の表面にヘアライン加工が施された表面加工部を有し、透明な被覆層を具えるマグネシウム合金部材は、金属質感が高められていることがわかる。 In this test, hairline processing with a surface roughness Rmax (maximum height) of 10 μm was performed. A panel test was conducted on any 10 persons for the obtained test material 2-A and the test material 1-B prepared in Test Example 1 (not subjected to hairline processing or diamond cutting). , 8 out of 10 respondents indicated that the test material 2-A had a higher metal texture and better design. From this result, it can be seen that the metal texture of the magnesium alloy member having the surface processed portion subjected to the hairline processing on the surface of the base material and having a transparent coating layer is enhanced.
[試験例3]
試験例1の試験材1-Aにおける塗装層の構成材料を変更した以外の点は、試験材1-Aと同様に作製した試料を試験材3-Aとし、外観についてパネル試験を行った。
[Test Example 3]
Except that the constituent material of the coating layer in the test material 1-A of Test Example 1 was changed, a sample produced in the same manner as the test material 1-A was used as the test material 3-A, and a panel test was performed on the appearance.
この試験では、基材に上記試験例1と同様の手順で下地処理及び防食層の形成を行い、その後、無色透明なフッ素樹脂(スミフロン:住友電気工業株式会社登録商標)を塗布して乾燥させる。この工程により、厚さ25μmの透明な塗装層を具える試験材3-Aが得られる。 In this test, the base treatment and the formation of the anticorrosion layer were performed on the substrate in the same procedure as in Test Example 1, and then a colorless transparent fluororesin (Sumiflon: Sumitomo Electric Industries, Ltd. registered trademark) was applied and dried. . By this step, a test material 3-A having a transparent coating layer having a thickness of 25 μm is obtained.
得られた試験材3-Aと、試験例1で作製した試験材1-B(ヘアライン加工やダイヤカット加工を施していないもの)とについて、任意の10人を対象としてパネルテストを実施したところ、10人中9人が試験材3-Aの方が金属質感が高く、意匠性に優れるという回答が得られた。 A panel test was conducted on 10 test subjects for the test material 3-A obtained and the test material 1-B produced in Test Example 1 (not subjected to hairline processing or diamond cutting). , 9 out of 10 respondents indicated that the test material 3-A had a higher metal texture and better design.
[試験例4]
試験例1の試験材1-Aのダイヤカット加工をエッチング加工に変更した以外の点は、試験材1-Aと同様に作製した試料を試験材4-1A,4-2Aとし、外観についてパネル試験を行った。
[Test Example 4]
Except for changing the diamond-cut processing of test material 1-A in Test Example 1 to etching, samples prepared in the same way as Test material 1-A are used as test materials 4-1A and 4-2A. A test was conducted.
試験材4-1Aのエッチング加工による表面加工部は、以下のように形成した。箱状のプレス材の表面にレジストを塗布した後、所定の模様のマスクを載せて露光し、光硬化していない部分を溶剤で剥離して所定の模様をパターニングした。その後、イオンミリング装置でプレス材(素材)が露出している部分に深さ10μmのドライエッチングを施し、最後にレジストを除去して、プレス材の突出した側の表面(約60×90mm)に所定の模様の凹凸を設けた。 The surface processed part of the test material 4-1A by etching was formed as follows. After applying a resist on the surface of the box-shaped press material, a predetermined pattern mask was placed on the surface for exposure, and the uncured portion was peeled off with a solvent to pattern the predetermined pattern. After that, dry etching with a depth of 10 μm is applied to the exposed part of the press material (material) with an ion milling device, and finally the resist is removed to form a surface (about 60 x 90 mm) on the protruding side of the press material. Unevenness of a predetermined pattern was provided.
試験材4-2Aのエッチング加工による表面加工部は、以下のように形成した。箱状のプレス材の表面にスクリーン印刷で所定の模様を印刷後、印刷していない部分を酸により深さ20μmのエッチングを施し、最後に印刷部分を除去して、プレス材の突出した側の表面(約60×90mm)に所定の模様の凹凸を設けた。 The surface processed part of the test material 4-2A by etching was formed as follows. After printing a predetermined pattern on the surface of the box-shaped press material by screen printing, the unprinted portion is etched with a depth of 20 μm with acid, and finally the printed portion is removed, and the protruding portion of the press material is removed. Irregularities with a predetermined pattern were provided on the surface (about 60 × 90 mm).
得られた試験材4-1A,4-2Aと試験例1で作製した試験材1-B(エッチング加工などの凹凸加工を施していないもの)とについて、任意の10人を対象としてパネルテストを実施した。その結果、10人中7人が試験材4-1Aの方が金属質感が高く、意匠性に優れるという回答が得られた。また、10人中8人が試験材4-2Aの方が金属質感が高く、意匠性に優れるという回答が得られた。 Panel test was conducted for any 10 persons with respect to the obtained test materials 4-1A and 4-2A and test material 1-B prepared in Test Example 1 (not subjected to uneven processing such as etching processing). Carried out. As a result, 7 out of 10 respondents indicated that the test material 4-1A had a higher metal texture and superior design. In addition, 8 out of 10 respondents indicated that test material 4-2A had a higher metal texture and superior design.
なお、上述した実施形態は、本発明の要旨を逸脱することなく、適宜変更することが可能であり、上述した構成に限定されるものではない。例えば、マグネシウム合金の組成、鋳造、圧延、及び塑性加工の条件、鋳造後及び圧延後の板厚、凹凸加工の形成方法、形成条件、被覆層の形成材料、形成方法などを適宜変更することができる。 The above-described embodiment can be appropriately changed without departing from the gist of the present invention, and is not limited to the above-described configuration. For example, the composition of the magnesium alloy, the conditions of casting, rolling, and plastic working, the plate thickness after casting and after rolling, the forming method of the uneven processing, the forming conditions, the forming material of the coating layer, the forming method, etc. may be appropriately changed. it can.
本発明マグネシウム合金部材は、金属質感が高いため、携帯電気機器類の筐体といった意匠性に優れることが望まれる分野に好適に利用することができる。 Since the magnesium alloy member of the present invention has a high metal texture, it can be suitably used in a field that is desired to have excellent design properties such as a casing of portable electric equipment.
Claims (11)
前記基材は、その表面の少なくとも一部に、金属質感が得られるように、微細な凹凸加工が施された表面加工部を具え、
前記被覆層は、透明であることを特徴とするマグネシウム合金部材。 A magnesium alloy member comprising a base material made of a magnesium alloy and a coating layer formed on the base material,
The base material has a surface processed portion on which fine unevenness is applied so that a metal texture is obtained on at least a part of the surface,
The magnesium alloy member, wherein the coating layer is transparent.
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