JP6132026B2 - Method for producing aluminum porous body - Google Patents
Method for producing aluminum porous body Download PDFInfo
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- JP6132026B2 JP6132026B2 JP2015539480A JP2015539480A JP6132026B2 JP 6132026 B2 JP6132026 B2 JP 6132026B2 JP 2015539480 A JP2015539480 A JP 2015539480A JP 2015539480 A JP2015539480 A JP 2015539480A JP 6132026 B2 JP6132026 B2 JP 6132026B2
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 181
- 229910052782 aluminium Inorganic materials 0.000 title claims description 122
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- 239000000843 powder Substances 0.000 claims description 98
- 229910000838 Al alloy Inorganic materials 0.000 claims description 76
- 239000011347 resin Substances 0.000 claims description 42
- 229920005989 resin Polymers 0.000 claims description 42
- 238000010438 heat treatment Methods 0.000 claims description 26
- 238000002844 melting Methods 0.000 claims description 24
- 230000008018 melting Effects 0.000 claims description 24
- 238000004891 communication Methods 0.000 claims description 22
- 239000012298 atmosphere Substances 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 11
- 230000001590 oxidative effect Effects 0.000 claims description 7
- 239000000758 substrate Substances 0.000 description 40
- 239000011148 porous material Substances 0.000 description 30
- 239000000523 sample Substances 0.000 description 29
- 238000000034 method Methods 0.000 description 18
- 239000006185 dispersion Substances 0.000 description 14
- 239000012530 fluid Substances 0.000 description 12
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 11
- 239000007788 liquid Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 238000010586 diagram Methods 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 8
- 239000002612 dispersion medium Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 5
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000007598 dipping method Methods 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 238000005245 sintering Methods 0.000 description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 229920005830 Polyurethane Foam Polymers 0.000 description 3
- 238000005275 alloying Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000005496 eutectics Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- 239000011812 mixed powder Substances 0.000 description 3
- 239000011496 polyurethane foam Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000007088 Archimedes method Methods 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000011859 microparticle Substances 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000002491 polymer binding agent Substances 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol 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
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000005489 elastic deformation Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D25/00—Special casting characterised by the nature of the product
- B22D25/005—Casting metal foams
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/11—Making porous workpieces or articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C7/00—Patterns; Manufacture thereof so far as not provided for in other classes
- B22C7/02—Lost patterns
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D21/00—Casting non-ferrous metals or metallic compounds so far as their metallurgical properties are of importance for the casting procedure; Selection of compositions therefor
- B22D21/002—Castings of light metals
- B22D21/007—Castings of light metals with low melting point, e.g. Al 659 degrees C, Mg 650 degrees C
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D25/00—Special casting characterised by the nature of the product
- B22D25/02—Special casting characterised by the nature of the product by its peculiarity of shape; of works of art
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D27/00—Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting
- B22D27/003—Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting by using inert gases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D27/00—Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting
- B22D27/15—Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting by using vacuum
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/11—Making porous workpieces or articles
- B22F3/1121—Making porous workpieces or articles by using decomposable, meltable or sublimatable fillers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/11—Making porous workpieces or articles
- B22F3/1121—Making porous workpieces or articles by using decomposable, meltable or sublimatable fillers
- B22F3/1137—Making porous workpieces or articles by using decomposable, meltable or sublimatable fillers by coating porous removable preforms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2301/00—Metallic composition of the powder or its coating
- B22F2301/05—Light metals
- B22F2301/052—Aluminium
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Powder Metallurgy (AREA)
Description
本発明は、三次元状に連結する骨格を有し、前記骨格により三次元状に連通する連通孔が形成される三次元網目状構造を有する多孔質体に関し、特に、骨格をアルミニウムもしくはアルミニウム合金で構成したアルミニウム系多孔質体およびその製造方法に関する。 The present invention relates to a porous body having a three-dimensional network structure in which three-dimensionally connected skeletons are formed and communication holes that are three-dimensionally communicated are formed by the skeleton, and in particular, the skeleton is made of aluminum or an aluminum alloy. Relates to an aluminum-based porous body constituted by the above and a method for producing the same.
三次元状に連結する骨格を有し、その骨格により三次元状に連通孔が形成される三次元網目状構造を有する多孔質体は、連通孔にガスあるいは液体等の流体を通過させるとともに、これらの流体を濾過処理するフィルター(特許文献1、2等)や、これらの流体を骨格表面に担持した触媒により改質する触媒用担体等(特許文献2等)に用いられている。 The porous body having a skeleton that is three-dimensionally connected and having a three-dimensional network structure in which communication holes are formed in three dimensions by the skeleton allows a fluid such as gas or liquid to pass through the communication holes, It is used for filters (Patent Documents 1 and 2 etc.) for filtering these fluids, and catalyst carriers and the like (Patent Document 2 and the like) for reforming these fluids with a catalyst supporting the surface of the skeleton.
このような三次元網目状構造を有する多孔質体は、連通孔を有する発泡樹脂骨格表面を導電化処理して電気メッキした後、加熱して樹脂を分解除去する方法(特許文献3等)や、連通孔を有する発泡樹脂に有機高分子結合剤と金属微小体との混練物を浸漬、スプレー等して塗着した後、加熱して樹脂を分解除去するとともに金属微小体を焼結する方法(特許文献1、2、4等)や、連通孔を有する発泡樹脂の骨格表面に粘着性を付与して粉体を付着させた後、加熱して樹脂を分解除去するとともに粉体を焼結する方法(特許文献5等)により製造される。 A porous body having such a three-dimensional network structure is obtained by conducting a conductive treatment on the surface of a foamed resin skeleton having communication holes and electroplating, followed by heating to decompose and remove the resin (Patent Document 3, etc.) A method in which a kneaded product of an organic polymer binder and a metal microparticle is applied to a foamed resin having communication holes by dipping, spraying, etc., and then heating to decompose and remove the resin and to sinter the metal microparticle (Patent Documents 1, 2, 4, etc.) and after applying adhesion to the skeleton surface of the foamed resin having communication holes and attaching the powder, it is heated to decompose and remove the resin and sinter the powder Manufactured by a method (Patent Document 5 or the like).
このような三次元網目状構造を有する多孔質体は、流体との接触面積が大きいことから、熱交換器の熱交換部品への適用が検討されている(特許文献6等)。熱交換器は、温度の高い物体から低い物体へ効率的に熱を移動させて加熱や冷却の用途に用いられる機器であり、一般に、熱交換の媒体として液体や気体等の流体を用いて流体に熱を与える(加熱)、もしくは流体から熱を奪う(冷却)ことで加熱や冷却を行う。このような熱交換器においては、熱伝導率の高い金属材料で構成されたフィン等を設けるなどして流体との接触面積を増加させて、熱交換の効率を高めているが、フィン等に替えて熱伝導率の高い金属材料で構成された三次元網目状構造を有する多孔質体を用い、その連通孔に流体を通過させれば、熱伝導率の高い金属材料と流体との接触面積をさらに大きくできるため、熱交換の効率がさらに大きくなるものと考えられる。 Since the porous body having such a three-dimensional network structure has a large contact area with a fluid, application to a heat exchange part of a heat exchanger has been studied (Patent Document 6 and the like). A heat exchanger is a device that is used for heating and cooling by efficiently transferring heat from a high-temperature object to a low-temperature object. In general, a fluid such as a liquid or a gas is used as a heat exchange medium. Heating or cooling is performed by applying heat to the fluid (heating) or by removing heat from the fluid (cooling). In such a heat exchanger, a fin made of a metal material having high thermal conductivity is provided to increase the contact area with the fluid to increase the efficiency of heat exchange. Instead, if a porous body having a three-dimensional network structure made of a metal material with high thermal conductivity is used and fluid is passed through the communication holes, the contact area between the metal material with high thermal conductivity and the fluid It is considered that the efficiency of heat exchange is further increased.
ところで、アルミニウムは軽量で熱伝導率が高いことから、三次元網目状構造多孔質体への適用が期待されている。しかしながら、アルミニウムは電気メッキをすることができず、特許文献3のような電気メッキによる製造が困難である。 By the way, since aluminum is lightweight and has high thermal conductivity, it is expected to be applied to a porous body having a three-dimensional network structure. However, aluminum cannot be electroplated and is difficult to manufacture by electroplating as in Patent Document 3.
また、特許文献4のように、連通孔を有する発泡樹脂に有機高分子結合剤とアルミニウム粉末との混練物を浸漬あるいはスプレー等して塗着した後、水素気流中520℃にて2時間加熱して樹脂を分解除去するとともに金属微小体を焼結する方法においては、アルミニウム粉末は表面に強固な酸化被膜(アルミナ:Al2O3)を有しており、上記方法で焼結してもアルミニウム粉末のごく一部で結合するに過ぎず、脆く、強度が極めて低いものしか製造することができない。Further, as in Patent Document 4, a kneaded product of an organic polymer binder and aluminum powder is applied to a foamed resin having communication holes by dipping or spraying, and then heated at 520 ° C. for 2 hours in a hydrogen stream. In this method, the aluminum powder has a strong oxide film (alumina: Al 2 O 3 ) on the surface and is sintered by the above method. Only a small portion of the aluminum powder is bonded, and only brittle and extremely low strength can be produced.
以上のことから、本発明は、表面に強固な酸化被膜を有するアルミニウム粉末およびアルミニウム合金粉末を用いて、これらの粉末が強固に結合して充分な強度を有する三次元網目状構造を有するアルミニウム系多孔質体およびその製造方法を提供することを目的とする。 In view of the above, the present invention uses an aluminum powder and an aluminum alloy powder having a strong oxide film on the surface, and the aluminum system having a three-dimensional network structure in which these powders are firmly bonded and have sufficient strength. It aims at providing a porous body and its manufacturing method.
本発明のアルミニウム系多孔質体は、三次元状に連結する骨格を有するとともに前記骨格により三次元状に連通する連通孔を有する三次元網目状構造体であって、前記骨格が、密度比が90%以上のアルミニウムもしくはアルミニウム合金からなるとともに、前記骨格の内部にアルミニウムの酸化物が分散することを特徴とする。なお、本発明における“アルミニウム”は、Al:95質量%以上で残部がC、N等の不純物からなり、他の金属元素を含まないもの、と定義する。 The aluminum-based porous body of the present invention is a three-dimensional network structure having a skeleton that is three-dimensionally connected and a communication hole that communicates three-dimensionally with the skeleton, wherein the skeleton has a density ratio. It is made of 90% or more of aluminum or aluminum alloy, and aluminum oxide is dispersed inside the skeleton. In the present invention, “aluminum” is defined as Al: 95% by mass or more, the balance being impurities such as C and N, and not containing other metal elements.
本発明のアルミニウム系多孔質体においては、骨格内部の密度比が90%以上であるため、骨格の強度が高く、また、この骨格にアルミニウムの酸化物(アルミナ:Al2O3)が分散することにより、アルミニウム基地を強化する結果、一層高い強度を示すものとなる。In the aluminum-based porous body of the present invention, since the density ratio inside the skeleton is 90% or more, the strength of the skeleton is high, and aluminum oxide (alumina: Al 2 O 3 ) is dispersed in this skeleton. As a result, the aluminum base is strengthened, resulting in higher strength.
上記のアルミニウム系多孔質体においては、骨格の強度の観点から、骨格内部の気孔の大きさは10μm以下であることが好ましい。また、アルミニウム基地を強化するアルミニウムの酸化物(アルミナ:Al2O3)についても、粗大であると骨格の強度がかえって低下することから、アルミニウムの酸化物の大きさ(最外径)は、10μm以下であることが好ましい。また、アルミニウムの酸化物は、骨格断面の面積率で5〜20%であることが望ましい。アルミニウムの酸化物が5%未満では基地強化の効果が乏しく、一方、20%を超えるものは製造が不可能である。この酸化物の骨格断面における面積率の測定についても、画像分析ソフトウエア(三谷産業製WinRoof等)を用いて、骨格断面の画像を自動二値化処理したり、該画像をグレースケールに変換して適当な閾値を設定したりすることにより、測定を行なうことができる。また、本発明のアルミニウム系多孔質体においては、上記骨格が中空状をなす形態を含む。In the above aluminum-based porous body, the size of pores inside the skeleton is preferably 10 μm or less from the viewpoint of the strength of the skeleton. Also, the aluminum oxide (alumina: Al 2 O 3 ) that reinforces the aluminum base also decreases the strength of the skeleton when it is coarse, so the size of the aluminum oxide (outermost diameter) is: It is preferable that it is 10 micrometers or less. The oxide of aluminum is preferably 5 to 20% in terms of the area ratio of the skeleton cross section. When the oxide of aluminum is less than 5%, the effect of strengthening the base is poor, while when it exceeds 20%, the production is impossible. For the measurement of the area ratio in the skeleton cross section of this oxide, the image of the skeleton cross section is automatically binarized using image analysis software (such as WinRoof made by Mitani Sangyo), or the image is converted to gray scale. Measurement can be performed by setting an appropriate threshold. In addition, the aluminum-based porous body of the present invention includes a form in which the skeleton is hollow.
また、本発明のアルミニウム系多孔質体は、三次元状に連結する骨格を有するとともに前記骨格により三次元状に連通する連通孔を有し、前記骨格が、アルミニウムもしくはアルミニウム合金からなる三次元網目状構造体であり、荷重を加えた際にひずみ量の増加に従って応力量が増加した後、骨格の圧壊に伴って応力がほぼ横ばいとなり、その後応力が増加する応力−ひずみ線図を示すことを特徴とする。 Further, the aluminum-based porous body of the present invention has a skeleton that is three-dimensionally connected and has a communication hole that communicates three-dimensionally with the skeleton, and the skeleton is made of aluminum or an aluminum alloy. It shows a stress-strain diagram in which the stress increases almost as the skeleton collapses after the stress increases as the strain increases when a load is applied, and then the stress increases. Features.
すなわち、特許文献4のようなアルミニウム多孔質体は、アルミニウム粉末どうしの結合が僅かであるため、応力を加えるとアルミニウム粉末どうしの結合が破断し、応力の増加に従ってアルミニウム粉末間の結合が破断していく。また、この破断に伴い、アルミニウム多孔質体より多数の破砕粒子が発生する。 That is, since the porous aluminum body as in Patent Document 4 has a slight bond between aluminum powders, the bond between aluminum powders breaks when stress is applied, and the bond between aluminum powders breaks as the stress increases. To go. Further, along with this breakage, a large number of crushed particles are generated from the aluminum porous body.
これを防止するためには、応力を加えた際に、アルミニウム粉末間の結合が破断することなく、ひずみ量の増加に従って応力が増加するような骨格とする必要がある。このような骨格が三次元状に連結する構造とすれば、アルミニウム粉末どうしの結合の破断が生じず、多数の破砕粒子の発生が防止される。 In order to prevent this, it is necessary to have a skeleton in which the stress increases as the strain amount increases without breaking the bond between the aluminum powders when stress is applied. If such a skeleton has a three-dimensionally connected structure, the aluminum powders are not broken and the generation of many crushed particles is prevented.
このような骨格を有するアルミニウム系多孔質体は、これに負荷されるある一定のひずみ量までは骨格が弾性変形するが、一定のひずみ量を超えると骨格が塑性変形して三次元状に連通する連通孔の圧壊が生じ、ひずみ量がさらに増加しても応力がほぼ横ばい(一定)の状態でアルミニウム系多孔質体の変形が進行する。さらに、アルミニウム系多孔質体に加わるひずみ量が増加して、三次元状に連通する連通孔の圧壊が終了した後、さらにひずみがアルミニウム系多孔質体に加わると、三次元状に連通する連通孔が閉塞したアルミニウム系多孔質体にひずみが生じて、ひずみ量の増加に従って応力が増加する。なお、骨格が変形する弾性限界は0.5MPa以上であることが望ましい。 An aluminum-based porous body having such a skeleton is elastically deformed up to a certain amount of strain applied to it, but when the amount exceeds a certain amount of strain, the skeleton is plastically deformed to communicate in a three-dimensional form. Even if the amount of strain further increases, deformation of the aluminum-based porous body proceeds while the stress is almost flat (constant). Furthermore, after the amount of strain applied to the aluminum-based porous body is increased and the crushing of the communication holes communicating in a three-dimensional shape is completed, if further strain is applied to the aluminum-based porous material, the communication communicating in a three-dimensional shape is performed. Strain is generated in the aluminum-based porous body in which the pores are closed, and the stress increases as the strain amount increases. The elastic limit for deformation of the skeleton is desirably 0.5 MPa or more.
このような応力−ひずみ線図を示すアルミニウム系多孔質体は、ある一定以上のひずみ量が負荷されたときに、アルミニウム粉末どうしの結合が強固であるため骨格が破断せず、塑性変形する。 The aluminum-based porous body showing such a stress-strain diagram is deformed plastically without breaking the skeleton because the bond between the aluminum powders is strong when a certain amount of strain is applied.
上記のアルミニウム系多孔質体においては、骨格の強度の観点から骨格内部の密度比が90%以上であることが好ましい。また、骨格内部の気孔の大きさは10μm以下であることが好ましい。 In the above-mentioned aluminum-based porous body, the density ratio inside the skeleton is preferably 90% or more from the viewpoint of the strength of the skeleton. The pore size inside the skeleton is preferably 10 μm or less.
さらに、上記の応力−ひずみ線図において、応力がほぼ横ばいとなった後、応力が増加するまで応力を加えた後に発生する破砕粒子の発生量が、アルミニウム系多孔質体の5質量%以下であることが好ましい。 Furthermore, in the above stress-strain diagram, the amount of crushed particles generated after applying the stress until the stress increases after the stress is almost flat is 5% by mass or less of the aluminum-based porous body. Preferably there is.
上記本発明に係るアルミニウム系多孔質体は、本発明のアルミニウム系多孔質体の製造方法によって得ることができる。すなわちその製造方法は、三次元状に連結する樹脂製の骨格を有し、前記樹脂製の骨格により三次元状に連通する連通孔が形成された樹脂製の三次元網目状構造体を基体とし、前記基体の樹脂製の骨格表面に、アルミニウム粉末および/またはアルミニウム合金粉末を付着させた後、非酸化性かつ10 −3 Pa以下の減圧雰囲気中で、前記アルミニウム粉末および/または前記アルミニウム合金粉末の融点以上に加熱して、前記基体を消失除去するとともに前記アルミニウム粉末および/または前記アルミニウム合金粉末を溶融することを特徴とする。 The aluminum-based porous body according to the present invention can be obtained by the method for producing an aluminum-based porous body of the present invention. That is, the manufacturing method is based on a resin-made three-dimensional network structure having a resin-made skeleton that is three-dimensionally connected and communication holes that are three-dimensionally communicated with the resin-made skeleton. After the aluminum skeleton and / or aluminum alloy powder is adhered to the resin skeleton surface of the base, the aluminum powder and / or the aluminum alloy powder in a non-oxidizing and reduced pressure atmosphere of 10 −3 Pa or less. It is characterized by being heated to a melting point of or higher and melting and removing the aluminum powder and / or the aluminum alloy powder.
本発明のアルミニウム系多孔質体の製造方法においては、三次元状に連結する樹脂製の骨格を有し、樹脂製の骨格により三次元状に連通する連通孔が形成される樹脂製の三次元網目状構造を基体とし、この基体の樹脂製の骨格表面に、アルミニウム粉末および/またはアルミニウム合金粉末を付着させた後、非酸化性雰囲気中で加熱して樹脂製の基体を消失除去する点は特許文献4と同様であるが、本発明においては、加熱温度をアルミニウム粉末および/またはアルミニウム合金粉末の融点以上としてアルミニウム粉末および/またはアルミニウム合金粉末を溶融させることが特徴である。本発明では、アルミニウム粉末またはアルミニウム合金粉末の平均粒径が1〜50μmであることを好ましい形態とする。また、上記加熱温度は上記融点+100℃以下であることを好ましい形態とする。 In the method for producing an aluminum-based porous body of the present invention, a resin-made three-dimensional structure in which a resin-made skeleton that is three-dimensionally connected and a communication hole that communicates three-dimensionally is formed by the resin-made skeleton. The point is that a network structure is used as a base, and after the aluminum powder and / or aluminum alloy powder is adhered to the surface of the resin skeleton of the base, the resin base is lost by heating in a non-oxidizing atmosphere. Although it is the same as that of Patent Document 4, the present invention is characterized in that the aluminum powder and / or aluminum alloy powder is melted at a heating temperature equal to or higher than the melting point of the aluminum powder and / or aluminum alloy powder. In this invention, it is set as the preferable form that the average particle diameter of aluminum powder or aluminum alloy powder is 1-50 micrometers. The heating temperature is preferably the melting point + 100 ° C. or less.
加熱する前の基体の樹脂製の骨格表面にアルミニウム粉末および/またはアルミニウム合金粉末を付着させた状態では、アルミニウム粉末および/またはアルミニウム合金粉末の表面は酸化被膜で覆われ、酸化被膜を介して各粉末粒子が接触している。そして、骨格表面にアルミニウム粉末および/またはアルミニウム合金粉末を付着させた基体を融点以上に加熱すると、昇温過程で樹脂製の基体が分解して消失するとともに、溶融したアルミニウムおよび/またはアルミニウム合金は、粉末の表面の酸化被膜を破って粉末表面を濡らして覆う。このとき粉末表面に形成されていた酸化被膜が代用骨格となり、溶融したアルミニウムおよび/またはアルミニウム合金がこの代用骨格の外側で濡れることにより、隣り合う粉末どうしが溶融したアルミニウムおよび/またはアルミニウム合金により結合される。このため、加熱後に得られるアルミニウム系多孔質体は、強固に金属結合しており、充分な結合を実現することができる。なお、本発明者等が銅粉末を用いて同様の実験を行ったところ、銅粉末が溶融して落下し、多孔質体を形成することができなかった。したがって、粉末を溶融させても形態を保持できるのは、酸化被膜を有するアルミニウムおよびアルミニウム合金特有の効果と言うことができる。 In a state in which the aluminum powder and / or aluminum alloy powder is adhered to the resin-made skeleton surface of the substrate before heating, the surface of the aluminum powder and / or aluminum alloy powder is covered with an oxide film, Powder particles are in contact. When a substrate having aluminum powder and / or aluminum alloy powder adhered to the skeleton surface is heated to a temperature higher than the melting point, the resin substrate decomposes and disappears during the temperature rising process, and the molten aluminum and / or aluminum alloy Break the oxide film on the surface of the powder to wet and cover the powder surface. At this time, the oxide film formed on the powder surface becomes a substitute skeleton, and molten aluminum and / or aluminum alloy wets outside the substitute skeleton, so that adjacent powders are bonded by molten aluminum and / or aluminum alloy. Is done. For this reason, the aluminum type porous body obtained after a heating has carried out the metal bond firmly, and can implement | achieve sufficient coupling | bonding. In addition, when the present inventors conducted a similar experiment using copper powder, the copper powder melted and dropped, and a porous body could not be formed. Therefore, it can be said that it is an effect peculiar to aluminum and an aluminum alloy having an oxide film that the shape can be maintained even when the powder is melted.
このようにして得られるアルミニウム系多孔質体の骨格は、密度比が例えば90%以上であるとともに、元の粉末表面に形成されていた酸化被膜すなわちアルミナ(Al2O3)が内部に分散するアルミニウムもしくはアルミニウム合金として形成される。アルミナは硬質であり、基地となるアルミニウムもしくはアルミニウム合金に分散して基地を強化する結果、アルミニウムもしくはアルミニウム合金は、高い強度を示すものとなる。なお、骨格の密度比はアルキメデス法で測定することができないため、骨格の断面を観察し、骨格断面の面積(中空部を除く基地部分)と骨格断面の基地部分に分散する気孔の面積率の差として計算する。骨格の断面面積および骨格の気孔の面積率の測定は、画像分析ソフトウエア(三谷産業製WinRoof等)を用いて、骨格断面の画像を自動二値化処理したり、該画像をグレースケールに変換して適当な閾値を設定したりすることにより、これらの面積率の測定を行なうことができる。The skeleton of the aluminum-based porous body thus obtained has a density ratio of, for example, 90% or more, and an oxide film formed on the surface of the original powder, that is, alumina (Al 2 O 3 ) is dispersed therein. It is formed as aluminum or an aluminum alloy. Alumina is hard and is dispersed in the base aluminum or aluminum alloy to strengthen the base. As a result, the aluminum or aluminum alloy exhibits high strength. Since the density ratio of the skeleton cannot be measured by the Archimedes method, the cross section of the skeleton is observed, and the area ratio of the pores dispersed in the skeleton cross section area (base part excluding the hollow part) and the base part of the skeleton cross section Calculate as the difference. To measure the cross-sectional area of the skeleton and the area ratio of the pores of the skeleton, the image of the skeleton cross-section is automatically binarized using image analysis software (such as WinRoof made by Mitani Sangyo), or the image is converted to gray scale. Then, these area ratios can be measured by setting an appropriate threshold value.
最終的なアルミニウム系多孔質体の三次元網目状構造は、基体の骨格表面に付着させて担持したアルミニウム粉末および/またはアルミニウム合金粉末を溶融することにより構成される。このため、基体の三次元網目状構造が、最終的なアルミニウム系多孔質体の三次元網目状構造に影響する。したがって、基体の三次元網目状構造を変更することで、所望の三次元網目状構造を有するアルミニウム系多孔質体を得ることができる。 The final three-dimensional network structure of the aluminum-based porous body is constituted by melting aluminum powder and / or aluminum alloy powder supported by being adhered to the surface of the skeleton of the substrate. For this reason, the three-dimensional network structure of the substrate affects the final three-dimensional network structure of the aluminum-based porous body. Therefore, an aluminum-based porous body having a desired three-dimensional network structure can be obtained by changing the three-dimensional network structure of the substrate.
三次元網目状構造のアルミニウム系多孔質体の骨格は、細すぎるとアルミニウム系多孔質体の強度が低下する。一方、太過ぎると連通する気孔を通過する流体の流れを阻害して圧力損失が大きくなる。アルミニウム系多孔質体の熱交換機への応用を考慮すると、骨格の太さは50〜500μmとすることが好ましい。 If the skeleton of the aluminum-based porous body having a three-dimensional network structure is too thin, the strength of the aluminum-based porous body decreases. On the other hand, if it is too thick, the flow of fluid passing through the communicating pores is hindered and the pressure loss increases. Considering application of the aluminum-based porous material to a heat exchanger, the thickness of the skeleton is preferably 50 to 500 μm.
また、アルミニウム系多孔質体の骨格は、基体の樹脂製の骨格の表面にアルミニウム粉末および/またはアルミニウム合金粉末を付着させ、溶融させて形成するが、基体の樹脂製の骨格の表面に付着させるアルミニウム粉末および/またはアルミニウム合金粉末の量が多くなると、溶融するアルミニウムおよび/またはアルミニウム合金の量が過多となり、表面張力による保形が難しくなり、型くずれが生じ易くなる。この観点から、樹脂製の骨格の表面に付着させるアルミニウム粉末および/またはアルミニウム合金粉末は、樹脂製の骨格の表面からの厚さが100〜1000μmとなるように付着させると、溶融の後に形成されるアルミニウムおよび/またはアルミニウム合金の骨格の太さが上記の50〜500μmに形成されることとなるので好ましい。 The skeleton of the aluminum-based porous body is formed by adhering and melting aluminum powder and / or aluminum alloy powder on the surface of the resin skeleton of the substrate, but is adhered to the surface of the resin skeleton of the substrate. When the amount of aluminum powder and / or aluminum alloy powder increases, the amount of molten aluminum and / or aluminum alloy becomes excessive, shape retention due to surface tension becomes difficult, and mold deformation tends to occur. From this point of view, the aluminum powder and / or the aluminum alloy powder to be adhered to the surface of the resin skeleton is formed after melting when adhered so that the thickness from the surface of the resin skeleton is 100 to 1000 μm. The thickness of the aluminum and / or aluminum alloy skeleton is preferably 50 to 500 μm.
上記のように基体の樹脂製の骨格の表面にアルミニウム粉末および/またはアルミニウム合金粉末を付着させる手法としては、アルミニウム粉末および/またはアルミニウム合金粉末を分散媒中に分散させるとともに、粘度を25℃の温度条件下において50〜1000Pa・sに調整した分散液を作製し、この分散液中に基体を浸漬した後、基体を乾燥させることで基体の樹脂製の骨格表面に、アルミニウム粉末および/またはアルミニウム合金粉末を付着させるといった形態が挙げられる。 As described above, the aluminum powder and / or aluminum alloy powder is adhered to the surface of the resin skeleton of the substrate as described above by dispersing the aluminum powder and / or aluminum alloy powder in a dispersion medium and having a viscosity of 25 ° C. A dispersion liquid adjusted to 50 to 1000 Pa · s under temperature conditions is prepared, and the substrate is immersed in the dispersion liquid, and then the substrate is dried, whereby aluminum powder and / or aluminum is formed on the resin-made skeleton surface. Examples include a form in which alloy powder is adhered.
本発明のアルミニウム系多孔質体は高い強度を示し、そして本発明のアルミニウム系多孔質体の製造方法により、そのような高い強度を示すアルミニウム系多孔質体を、簡便な方法で量産性に富み、かつ、安価に製造することができるといった効果が奏される。 The aluminum-based porous material of the present invention exhibits high strength, and the aluminum-based porous material exhibiting such high strength can be easily mass-produced by a simple method by the method for producing the aluminum-based porous material of the present invention. And the effect that it can manufacture cheaply is show | played.
以下、本発明の一実施形態を説明する。
[基体]
基体は、三次元状に連結する骨格を有し、その骨格により三次元状に連結する気孔が形成される三次元網目状構造体を用いる。この基体は骨格表面にアルミニウム粉末および/またはアルミニウム合金粉末を付着させて担持するものであり、加熱されて分解、消失すべきものであることから、樹脂により構成される。具体的には、基体としてポリウレタンフォームが最も一般的に用いられるが、他にシリコーン樹脂、ポリエステル樹脂のフォームなどを用いることができる。Hereinafter, an embodiment of the present invention will be described.
[Substrate]
The substrate uses a three-dimensional network structure having a skeleton that is three-dimensionally connected and pores that are three-dimensionally connected by the skeleton. This substrate is supported by adhering aluminum powder and / or aluminum alloy powder to the surface of the skeleton, and is composed of a resin because it should be decomposed and disappeared by heating. Specifically, polyurethane foam is most commonly used as the substrate, but silicone resin, polyester resin foam, and the like can also be used.
[アルミニウム粉末またはアルミニウム合金粉末]
基体の樹脂骨格に付着させる粉末は、上記のとおり、熱伝導率および比重のバランスよりアルミニウム粉末を用いるが、アルミニウム粉末に替えて、アルミニウムを強化する成分を予め合金化したアルミニウム合金粉末を用いてもよい。たとえば、AlにCu、Mn、Mg、Si等の合金化元素を予合金化したアルミニウム合金粉末を用いた場合は、アルミニウム系多孔質体の骨格がアルミニウム合金で形成され、アルミニウム系多孔質体の強度を向上させることができる。AlにCu、Mn、Mg、Si等の合金化元素を添加することにより、熱伝導率はAl単体の場合よりも低下するが、ベース金属がAlであるため、充分に高い熱伝導率を維持することができる。アルミニウム粉末またはアルミニウム合金粉末は、一般的なもの、すなわち表面に10Å程度の酸化被膜(アルミナ:Al2O3)を有するものを用いる。[Aluminum powder or aluminum alloy powder]
As described above, an aluminum powder is used as the powder to be attached to the resin skeleton of the base body in view of the balance of thermal conductivity and specific gravity. Instead of the aluminum powder, an aluminum alloy powder obtained by previously alloying a component that strengthens aluminum is used. Also good. For example, when aluminum alloy powder in which alloying elements such as Cu, Mn, Mg, and Si are prealloyed is used for Al, the skeleton of the aluminum-based porous body is formed of the aluminum alloy, and the aluminum-based porous body Strength can be improved. By adding alloying elements such as Cu, Mn, Mg, and Si to Al, the thermal conductivity is lower than that of Al alone, but the base metal is Al, so it maintains a sufficiently high thermal conductivity. can do. As the aluminum powder or aluminum alloy powder, a general one, that is, a powder having an oxide film (alumina: Al 2 O 3 ) of about 10 mm on the surface is used.
基体の樹脂骨格に付着させるアルミニウム粉末および/またはアルミニウム合金粉末は、細い基体の樹脂骨格表面に密に付着できることから微細なものが好ましい。粉末が大きくなると基体の樹脂骨格表面に密に付着させることが難しくなるとともに、粉末の質量が増加することにより、基体の樹脂骨格表面に付着し難くなったり、脱落し易くなったりする。この観点からアルミニウム粉末および/またはアルミニウム合金粉末は、平均粒径が50μm以下のものを用いることが好ましい。さらに、平均粒径が50μm以下であるとともに、粒径が100μmを超える粉末を含まないものであることが好ましい。ただし、Alは活性な金属であるため、あまりに微細な粉末は取扱いが難しくなる。この観点からアルミニウム粉末および/またはアルミニウム合金粉末は、平均粒径が1μm以上のものを用いることが好ましい。 The aluminum powder and / or aluminum alloy powder to be adhered to the resin skeleton of the substrate is preferably a fine one because it can adhere closely to the surface of the resin skeleton of the thin substrate. When the powder becomes large, it becomes difficult to adhere closely to the resin skeleton surface of the substrate, and due to the increase in the mass of the powder, it becomes difficult to adhere to the resin skeleton surface of the substrate, or it tends to fall off. From this viewpoint, it is preferable to use an aluminum powder and / or an aluminum alloy powder having an average particle size of 50 μm or less. Furthermore, it is preferable that the average particle size is 50 μm or less and does not contain powder having a particle size exceeding 100 μm. However, since Al is an active metal, it is difficult to handle an excessively fine powder. From this viewpoint, it is preferable to use an aluminum powder and / or an aluminum alloy powder having an average particle size of 1 μm or more.
[付着工程]
基体の樹脂骨格へアルミニウム粉末および/またはアルミニウム合金粉末を付着させるにあたっては、従来から行われている各種方法を適用することができる。以下に代表的な方法を記載する。[Adhesion process]
Various conventional methods can be applied to adhere the aluminum powder and / or aluminum alloy powder to the resin skeleton of the substrate. A typical method is described below.
(1)湿式法
特許文献1、2、4等に記載された方法であり、アルミニウム粉末および/またはアルミニウム合金粉末を分散媒中に分散させた分散液を作成し、この分散液中に基体を浸漬した後、基体を乾燥させる方法である。分散媒としては、アルコール等の揮発性を有する液体や水を溶媒とし、これに結着剤を溶解した液を用いることができる。この場合、粉末が沈降しないよう分散媒に分散剤を添加してもよい。また、分散媒としては、フェノール樹脂等の高分子有機物の溶液を用いてもよい。(1) Wet method A method described in Patent Documents 1, 2, 4, etc., in which a dispersion liquid in which aluminum powder and / or aluminum alloy powder is dispersed in a dispersion medium is prepared, and a substrate is placed in the dispersion liquid. After dipping, the substrate is dried. As the dispersion medium, a liquid having a volatile property such as alcohol or water as a solvent and a binder dissolved therein can be used. In this case, a dispersant may be added to the dispersion medium so that the powder does not settle. Moreover, as a dispersion medium, you may use the solution of high molecular organic substances, such as a phenol resin.
このとき、分散液の粘度により基体の樹脂骨格の表面に付着するアルミニウム粉末および/またはアルミニウム合金粉末を制御することができる。すなわち、分散液の粘度が高ければ、基体の樹脂骨格の表面に付着するアルミニウム粉末および/またはアルミニウム合金粉末の量が多くなり、逆に、分散液の粘度が低ければ、基体の樹脂骨格の表面に付着するアルミニウム粉末および/またはアルミニウム合金粉末の量が少なくなる。ただし、分散液の粘度が過多となると、基体の樹脂骨格の表面に付着するアルミニウム粉末および/またはアルミニウム合金粉末の量が過多となり、樹脂製の骨格の表面からの厚さが1000μmを超えて、後述する加熱工程において型くずれが生じ易くなる。この観点から、分散液の粘度は25℃の温度条件下において1000Pa・s以下とすることが好ましい。一方、分散液の粘度が低すぎると、基体の樹脂骨格の表面に付着するアルミニウム粉末および/またはアルミニウム合金粉末の量が乏しくなり、加熱工程後に得られる三次元網目状構造のアルミニウム系多孔質体の骨格が細くなり、アルミニウム系多孔質体の強度が低下する。この観点から、分散液の粘度は25℃の温度条件下において50Pa・s以上とすることが好ましい。なお、粘度の測定は、東機産業株式会社製TVB10形粘度計等を用いて、粘性トルクによる2枚のスリット円板のねじれ角を検出して粘度に換算することにより行うことができる。 At this time, the aluminum powder and / or aluminum alloy powder adhering to the surface of the resin skeleton of the substrate can be controlled by the viscosity of the dispersion. That is, when the viscosity of the dispersion liquid is high, the amount of aluminum powder and / or aluminum alloy powder adhering to the surface of the resin skeleton of the substrate increases. Conversely, when the viscosity of the dispersion liquid is low, the surface of the resin skeleton of the substrate is increased. The amount of aluminum powder and / or aluminum alloy powder adhering to the surface is reduced. However, if the viscosity of the dispersion becomes excessive, the amount of aluminum powder and / or aluminum alloy powder adhering to the surface of the resin skeleton of the substrate becomes excessive, and the thickness from the surface of the resin skeleton exceeds 1000 μm, Mold deformation is likely to occur in the heating process described later. From this viewpoint, the viscosity of the dispersion liquid is preferably 1000 Pa · s or less under a temperature condition of 25 ° C. On the other hand, if the viscosity of the dispersion is too low, the amount of aluminum powder and / or aluminum alloy powder adhering to the surface of the resin skeleton of the substrate becomes small, and the aluminum-based porous body having a three-dimensional network structure obtained after the heating step The skeleton of the material becomes thinner, and the strength of the aluminum-based porous body decreases. From this viewpoint, the viscosity of the dispersion is preferably 50 Pa · s or more under a temperature condition of 25 ° C. The viscosity can be measured by detecting the twist angle of the two slit disks due to the viscous torque and converting the viscosity into a viscosity using a TVB10 viscometer manufactured by Toki Sangyo Co., Ltd.
(2)乾式法
特許文献5に記載された方法であり、基体表面にアクリル系、ゴム系等の粘着剤溶液またはフェノール樹脂、エポキシ樹脂、フラン樹脂等接着性の樹脂溶液を塗布することにより粘着性を付与し、粉体中で基体を揺動させるか、あるいは基体に粉体をスプレーする等の方法により、骨格表面に粉体を被着させる方法である。(2) Dry method This is a method described in Patent Document 5, and is applied by applying an adhesive solution such as an acrylic or rubber adhesive or an adhesive resin solution such as a phenol resin, epoxy resin or furan resin to the surface of the substrate. This is a method in which the powder is deposited on the surface of the skeleton by a method such as imparting properties and swinging the substrate in the powder or spraying the powder on the substrate.
[加熱工程]
骨格表面にアルミニウム粉末またはアルミニウム合金粉末を付着させた基体は、非酸化性雰囲気中で、アルミニウム粉末および/またはアルミニウム合金粉末の融点以上に加熱される。この融点までの昇温過程で樹脂製の基体は分解し除去されて消失する。[Heating process]
The substrate on which the aluminum powder or the aluminum alloy powder is adhered to the surface of the skeleton is heated to the melting point or higher of the aluminum powder and / or the aluminum alloy powder in a non-oxidizing atmosphere. In the process of raising the temperature to the melting point, the resin substrate is decomposed and removed to disappear.
加熱温度がアルミニウム(融点:660.4℃)もしくはアルミニウム合金の融点を超えると、アルミニウム粉末もしくはアルミニウム合金粉末が内部で溶融する。すなわち、アルミニウム粉末もしくはアルミニウム合金粉末の表面は酸化被膜(アルミナ:Al2O3)で覆われており、アルミナの融点は2072℃と高いためアルミニウム粉末もしくはアルミニウム合金粉末の表面の酸化被膜が溶融せず、これらの粉末の内部が溶融する。このようにして内部で溶融したアルミニウムまたはアルミニウム合金は、図1に示すように、粉末の表面の酸化被膜を破って粉末表面に濡れて覆うとともに、各粉末から発生した溶融アルミニウムまたは溶融アルミニウム合金が混ざり合い結合する。このとき粉末表面に形成されていた酸化被膜が代用骨格となり、骨格の形状を維持するとともに、互いに結合した溶融アルミニウムまたは溶融アルミニウム合金の表面張力により骨格表面は比較的滑らかとなりネック部が消失して連続する金属表面となる。When the heating temperature exceeds the melting point of aluminum (melting point: 660.4 ° C.) or aluminum alloy, the aluminum powder or aluminum alloy powder melts inside. That is, the surface of the aluminum powder or aluminum alloy powder is covered with an oxide film (alumina: Al 2 O 3 ), and the melting point of alumina is as high as 2072 ° C., so the oxide film on the surface of the aluminum powder or aluminum alloy powder melts. The inside of these powders melts. As shown in FIG. 1, the aluminum or aluminum alloy thus melted inside breaks the oxide film on the surface of the powder and wets the powder surface, and the molten aluminum or molten aluminum alloy generated from each powder Mix and combine. At this time, the oxide film formed on the powder surface becomes a substitute skeleton, maintains the shape of the skeleton, and the surface tension of the molten aluminum or molten aluminum alloy bonded to each other makes the skeleton surface relatively smooth and the neck portion disappears. It becomes a continuous metal surface.
このようにして得られるアルミニウム系多孔質体の骨格は、元の粉末表面に形成されていた酸化被膜すなわちアルミナ(Al2O3)が内部に分散するアルミニウムもしくはアルミニウム合金として形成される。このアルミナは硬質であり、基地となるアルミニウムもしくはアルミニウム合金に分散して基地の強化に寄与する。また、骨格は、樹脂製の骨格が存在していた部分に空洞を有する中空状をなしているので、軽量化が求められる用途に有効である。The skeleton of the aluminum-based porous body thus obtained is formed as aluminum or an aluminum alloy in which the oxide film formed on the original powder surface, that is, alumina (Al 2 O 3 ) is dispersed. This alumina is hard and contributes to strengthening of the base by being dispersed in the base aluminum or aluminum alloy. Moreover, since the skeleton has a hollow shape having a cavity in the portion where the resin skeleton was present, it is effective for applications that require weight reduction.
一方、加熱温度がアルミニウムもしくはアルミニウム合金の融点未満の場合には、図2に示すように、アルミニウム粉末またはアルミニウム合金粉末の表面に形成された強固な酸化被膜がバリヤとなって、アルミニウム粉末どうし、またはアルミニウム合金粉末どうしの拡散による接合を阻害して焼結が進行しない。 On the other hand, when the heating temperature is lower than the melting point of aluminum or aluminum alloy, as shown in FIG. 2, a strong oxide film formed on the surface of the aluminum powder or aluminum alloy powder becomes a barrier, and the aluminum powders are Alternatively, the sintering does not proceed because the bonding due to the diffusion of the aluminum alloy powders is hindered.
加熱工程における雰囲気が大気等の酸化性の雰囲気であると、粉末表面の酸化被膜を破って露出した溶融アルミニウムまたは溶融アルミニウム合金が直ちに酸化され、粉末表面に濡れて覆ったり、各粉末から発生した溶融アルミニウムまたは溶融アルミニウム合金が混ざり合ったりすることが阻止され、粉末どうしの結合が阻害される。このため、加熱工程における雰囲気は窒素ガス、不活性ガス等の非酸化性の雰囲気とすることが望ましい。なお、上記の加熱工程は、アルミニウム粉末もしくはアルミニウム合金粉末の表面の酸化被膜を除去することは目的ではないため、水素ガスもしくは水素混合ガス等の還元性の雰囲気である必要はないが、還元性の雰囲気は非酸化性の雰囲気であるため、還元性の雰囲気としてもよい。また、圧力が10−3Pa以下の減圧雰囲気(真空雰囲気)としてもよい。When the atmosphere in the heating process is an oxidizing atmosphere such as the air, the molten aluminum or molten aluminum alloy exposed by breaking the oxide film on the powder surface is immediately oxidized and wetted or covered with the powder surface, or generated from each powder. Mixing of molten aluminum or molten aluminum alloy is prevented, and bonding of powders is inhibited. For this reason, it is desirable that the atmosphere in the heating step be a non-oxidizing atmosphere such as nitrogen gas or inert gas. The above heating step is not intended to remove the oxide film on the surface of the aluminum powder or aluminum alloy powder, so it is not necessary to be in a reducing atmosphere such as hydrogen gas or a hydrogen mixed gas. Since this atmosphere is a non-oxidizing atmosphere, it may be a reducing atmosphere. Moreover, it is good also as a pressure-reduced atmosphere (vacuum atmosphere) whose pressure is 10 < -3 > Pa or less.
なお、加熱温度は基体に付着させたアルミニウム粉末もしくはアルミニウム合金粉末の融点を超える温度であれば粉末を溶融できるが、融点を大きく超える温度で加熱するとその分余分なエネルギーが必要となるとともに、溶融したアルミニウムもしくはアルミニウム合金の粘度が低下して型崩れが生じ易くなることから、加熱温度は融点+100℃までとすることが好ましい。 The heating temperature can be melted as long as the temperature exceeds the melting point of the aluminum powder or aluminum alloy powder adhered to the substrate. However, heating at a temperature greatly exceeding the melting point requires extra energy and melting. The heating temperature is preferably up to the melting point + 100 ° C., because the viscosity of the aluminum or aluminum alloy is lowered and the mold is likely to lose its shape.
三次元網目状構造のアルミニウム系多孔質体の骨格は、細すぎるとアルミニウム系多孔質体の強度が低下する。一方、太くなると連通する気孔を通過する流体の流れを阻害して圧力損失が大きくなる。また、アルミニウム系多孔質体の骨格は、基体の樹脂製骨格の表面にアルミニウム粉末もしくはアルミニウム合金粉末を付着させ、溶融させて形成するが、基体の樹脂製骨格の表面に付着するアルミニウム粉末もしくはアルミニウム合金粉末の量が多くなると、溶融したアルミニウムもしくはアルミニウム合金の量が多くなるが、溶融したアルミニウムもしくはアルミニウム合金の量が過多となると、表面張力による保形が難しくなり、型くずれが生じ易くなる。このため、アルミニウム系多孔質体の骨格の太さは50〜500μmとすることが好ましい。また、樹脂製の骨格の表面に付着させるアルミニウム粉末またはアルミニウム合金粉末の量は、樹脂製の骨格の表面からの厚さが100〜1000μmとなるように付着させると、溶融の後に形成されるアルミニウムおよび/またはアルミニウム合金の骨格の太さが上記の50〜500μmに形成されることとなるので好ましい。 If the skeleton of the aluminum-based porous body having a three-dimensional network structure is too thin, the strength of the aluminum-based porous body decreases. On the other hand, when the thickness increases, the flow of fluid passing through the communicating pores is hindered, and the pressure loss increases. The skeleton of the aluminum-based porous body is formed by adhering and melting aluminum powder or aluminum alloy powder on the surface of the resin skeleton of the base, but the aluminum powder or aluminum adhering to the surface of the resin skeleton of the base is used. When the amount of alloy powder increases, the amount of molten aluminum or aluminum alloy increases. However, when the amount of molten aluminum or aluminum alloy is excessive, shape retention due to surface tension becomes difficult, and mold deformation tends to occur. For this reason, the thickness of the skeleton of the aluminum-based porous material is preferably 50 to 500 μm. In addition, the amount of aluminum powder or aluminum alloy powder to be adhered to the surface of the resin skeleton is such that the aluminum formed after melting when the thickness from the surface of the resin skeleton is 100 to 1000 μm. And / or the thickness of the skeleton of the aluminum alloy is preferably 50 to 500 μm.
上記の製造方法によって製造したアルミニウム系多孔質体の三次元網目状構造は、樹脂製基体の三次元網目状構造がそのまま維持されたものとなる。したがって、樹脂製基体の三次元網目状構造を変更することで、アルミニウム系多孔質体の三次元網目状構造を変更することができ、アルミニウム系多孔質体全体の気孔率、気孔の大きさを所望のものに調整することが可能である。具体的には、気孔率は80〜95%のもの、好ましくは85〜95%のものとすることができ、気孔の大きさは30〜4000μmのものとすることができ、6〜80ppi(セル数/25.4mm)の多孔質体を容易に製造することができる。 The three-dimensional network structure of the aluminum-based porous body manufactured by the above manufacturing method is the one in which the three-dimensional network structure of the resin base is maintained as it is. Therefore, by changing the three-dimensional network structure of the resin substrate, the three-dimensional network structure of the aluminum porous body can be changed, and the porosity and pore size of the entire aluminum porous body can be changed. It is possible to adjust to the desired one. Specifically, the porosity can be 80-95%, preferably 85-95%, the pore size can be 30-4000 μm, and 6-80 ppi (cell Several / 25.4 mm) can be easily manufactured.
なお、アルミニウム合金によりアルミニウム系多孔質体を構成する場合において、原料粉末としてAlと共晶液相を発生する成分(Cu、Mg等)を単味粉末あるいはアルミニウム合金粉末として、アルミニウム粉末に添加したアルミニウム系混合粉末を用い、三次元網目状構造を有する樹脂製の基体の表面にアルミニウム系混合粉末を付着させ、共晶液相が発生する温度で焼結を行う方法が考えられるが、この方法では、アルミニウム系多孔質体中の成分元素の分布が不均一となるとともに、骨格内部にアルミニウムの酸化物が分散せず、所望の強度を得ることが難しい。 In the case of forming an aluminum-based porous body with an aluminum alloy, a component (Cu, Mg, etc.) that generates a eutectic liquid phase with Al as a raw material powder was added to the aluminum powder as a simple powder or an aluminum alloy powder. A method of using an aluminum-based mixed powder, attaching the aluminum-based mixed powder to the surface of a resin substrate having a three-dimensional network structure, and sintering at a temperature at which a eutectic liquid phase is generated can be considered. Then, the distribution of the component elements in the aluminum-based porous body becomes non-uniform, and the oxide of aluminum is not dispersed inside the skeleton, so that it is difficult to obtain a desired strength.
これに対して、上述のように予め成分元素をAl中に合金化させたアルミニウム予合金粉末を用いることにより、アルミニウム系多孔質体中の成分元素の分布が均一となる。また、製法に起因するアルミニウムの酸化物が骨格内部に分散する。このため、アルミニウム系混合粉末を用いて共晶液相により焼結する方法に比して、高い強度を得ることができる。 On the other hand, the distribution of the component elements in the aluminum-based porous body becomes uniform by using the aluminum prealloy powder in which the component elements are previously alloyed in Al as described above. In addition, aluminum oxide resulting from the manufacturing method is dispersed inside the skeleton. For this reason, high intensity | strength can be acquired compared with the method of sintering by a eutectic liquid phase using aluminum type mixed powder.
三次元網目状構造を有する樹脂製の基体として、縦10mm、横20mm、厚さ10mmのポリウレタンフォーム(商品名エバーライトSF、株式会社ブリヂストン製)を用意した。このポリウレタンフォームは、気孔率(全体の体積に対する連通孔の体積の割合)が95%であり、連通孔の大きさが円相当径で3000μmであった。次いで、分散媒として樹脂分1質量%のポリビニルアルコール(商品名:ゴーセノールGH−23、日本合成化学工業株式会社製)を用意し、平均粒径6μmのアルミニウム粉末を用意した分散媒に質量比1:1で混合し、アルミニウム粉末分散液(25℃における粘度:50〜75Pa・s:東機産業株式会社製TVB10形粘度計により測定)を作製した。作製したアルミニウム粉末分散液に用意した基体を浸漬した後、余分なスラリーをロールにより除去した後、100℃にて120分乾燥させて、アルミニウム粉末が付着した基体を用意した。このようにして作製したアルミニウム粉末が付着した基体を、圧力が10−3Paの減圧雰囲気(真空雰囲気)の下、表1に示す加熱温度にて210分間加熱し、試料番号01〜07の多孔質試料を作製した。A polyurethane foam (trade name Everlight SF, manufactured by Bridgestone Corporation) having a length of 10 mm, a width of 20 mm, and a thickness of 10 mm was prepared as a resin base having a three-dimensional network structure. This polyurethane foam had a porosity (ratio of the volume of communication holes to the total volume) of 95%, and the size of the communication holes was 3000 μm in terms of the equivalent circle diameter. Next, polyvinyl alcohol (trade name: Gohsenol GH-23, manufactured by Nippon Synthetic Chemical Industry Co., Ltd.) having a resin content of 1% by mass was prepared as a dispersion medium, and a mass ratio of 1 to a dispersion medium prepared with aluminum powder having an average particle size of 6 μm. 1 was mixed to prepare an aluminum powder dispersion (viscosity at 25 ° C .: 50 to 75 Pa · s: measured with TVB10 viscometer manufactured by Toki Sangyo Co., Ltd.). After dipping the prepared substrate in the prepared aluminum powder dispersion, excess slurry was removed by a roll and then dried at 100 ° C. for 120 minutes to prepare a substrate to which aluminum powder was adhered. The substrate to which the aluminum powder thus prepared was attached was heated for 210 minutes at a heating temperature shown in Table 1 under a reduced pressure atmosphere (vacuum atmosphere) having a pressure of 10 −3 Pa, and the porous bodies of sample numbers 01 to 07 were used. A quality sample was prepared.
これらの多孔質試料について、アルキメデス法にて気孔率を測定した。また、光学顕微鏡にて観察し、画像分析ソフトウエア(三谷産業製WinRoof)を用いて、気孔の大きさについて測定するとともに三次元網目構造の気孔(連通孔)の円相当直径について求めその平均値を求めた。 The porosity of these porous samples was measured by the Archimedes method. In addition, by observing with an optical microscope and measuring the size of the pores using image analysis software (WinRoof manufactured by Mitani Sangyo), the average value of the equivalent circle diameters of the pores (communication holes) of the three-dimensional network structure is obtained. Asked.
また、多孔質試料を樹脂に埋め込み、鏡面研磨してケラー氏液(塩酸0.5ml,硝酸2.5ml,フッ酸1.5ml,蒸留水95ml)にて腐食を行い、骨格部の金属組織を観察し、画像分析ソフトウエア(三谷産業製WinRoof)を用いて、画像を二値化し、骨格部(中空部を除く基地部分)の面積率および骨格部(中空部を除く基地部分)に分散する気孔の断面面積率を測定して骨格部の密度比を求めた。また、EPMA装置で骨格部断面のうち中空部を除く基地部分の金属組織を5000倍で観察し、骨格部断面に分散する酸化物の大きさについて、同様にして画像分析ソフトウエア(三谷産業製WinRoof)を用いて、バレー法にて閾値180として180以上となる領域(180〜255)の面積を測定し酸化物の大きさおよび断面面積率を測定した。これらの結果を表1に示す。 In addition, a porous sample is embedded in resin, mirror-polished, and corroded with Keller's solution (hydrochloric acid 0.5 ml, nitric acid 2.5 ml, hydrofluoric acid 1.5 ml, distilled water 95 ml), and the metal structure of the skeleton part is obtained. Observe and binarize the image using image analysis software (WinRoof made by Mitani Sangyo) and disperse the area ratio of the skeleton part (base part excluding the hollow part) and the skeleton part (base part excluding the hollow part) The cross-sectional area ratio of the pores was measured to determine the density ratio of the skeleton. In addition, the metal structure of the base part excluding the hollow part in the cross section of the skeleton part was observed with a magnification of 5,000 times with an EPMA apparatus, and the size of the oxide dispersed in the cross section of the skeleton part was similarly analyzed using image analysis software (Mitani Sangyo Using WinRoof), the area of a region (180 to 255) having a threshold value 180 of 180 or more was measured by the valley method, and the oxide size and the cross-sectional area ratio were measured. These results are shown in Table 1.
さらに試料番号01〜07のアルミニウム系多孔質体試料について、圧縮降伏試験を行って圧縮荷重を増加させたときのひずみ量と応力を測定し、応力−ひずみ線図を作成した。そして、作成した応力−ひずみ線図から、応力がほぼ横ばいになる領域(プラトー領域)に至ったときの応力を求め、その結果を表1に併記した。 Furthermore, about the aluminum type porous body sample of sample numbers 01-07, the compression yield test was done and the amount of strain and stress when a compression load was increased were measured, and the stress-strain diagram was created. And the stress when it reached the area | region (plateau area | region) where stress became substantially flat was calculated | required from the created stress-strain diagram, and the result was written together in Table 1.
表1より試料番号01〜07のいずれの多孔質試料も気孔率が基体として用いたウレタンフォームとほぼ同じであり、また連通孔の大きさも、基体のウレタンフォームとほぼ同じ大きさとなっている。この結果から、基体のウレタンフォームの気孔率および連通孔の大きさが、そのまま多孔質試料の気孔率および連通孔の大きさとなることが確認された。 According to Table 1, the porous samples of sample numbers 01 to 07 have the same porosity as the urethane foam used as the substrate, and the size of the communicating holes is almost the same as the urethane foam of the substrate. From this result, it was confirmed that the porosity of the urethane foam as a base and the size of the communication holes were directly the porosity and the size of the communication holes of the porous sample.
しかしながら、加熱温度がアルミニウムの融点(660℃)に満たない試料番号01〜03の試料では、焼結が進行せず、骨格部の密度比が低い値となっている。 However, in the samples of sample numbers 01 to 03 whose heating temperature is less than the melting point (660 ° C.) of aluminum, sintering does not proceed and the density ratio of the skeleton is low.
一方、加熱温度がアルミニウムの融点(660℃)を超える04〜07の試料では、骨格部の密度比が90%以上となり、高い密度比を示している。また、04〜07の試料において、骨格部の気孔の大きさは2〜10μmと小さいものである。さらに、04〜07の試料では、骨格部の内部に酸化物の分散が認められ、酸化物は大きさが10μm、断面面積率が8面積%であった。一方、比較例である01〜03の試料は、アルミニウム粉末がごく一部で結合するのみであり酸化物はアルミニウム粉末表面にのみ認められ基地内部に分散する酸化物は認められなかった。 On the other hand, in the sample of 04-07 whose heating temperature exceeds the melting point (660 ° C.) of aluminum, the density ratio of the skeleton is 90% or higher, indicating a high density ratio. In the samples 04 to 07, the size of the pores in the skeleton is as small as 2 to 10 μm. Furthermore, in the samples of 04 to 07, oxide dispersion was observed inside the skeleton, and the oxide had a size of 10 μm and a cross-sectional area ratio of 8 area%. On the other hand, in the samples of 01 to 03 which are comparative examples, only a part of the aluminum powder was bonded, the oxide was observed only on the surface of the aluminum powder, and the oxide dispersed inside the matrix was not recognized.
本発明例である試料番号04の多孔質試料の気孔状態を観察した写真を図3に示す。図3に示すように、本発明例の多孔質試料は、溶融アルミニウムが隣り合う粉末を結合するとともに、溶融アルミニウムの表面張力により骨格表面は比較的に滑らかとなりネック部が消失して連続する金属表面となっている。 The photograph which observed the pore state of the porous sample of the sample number 04 which is an example of this invention is shown in FIG. As shown in FIG. 3, the porous sample of the example of the present invention is a metal in which molten aluminum binds adjacent powders, and the surface of the skeleton is relatively smooth due to the surface tension of molten aluminum, and the neck portion disappears and continues. It is the surface.
本発明例のアルミニウム系多孔質体について、骨格部断面を電子線微小分析装置(EPMA:Electron Probe MicroAnalyser)で観察したときの走査型電子顕微鏡(SEM:Scanning Electron Microscope)写真およびAlとO(酸素)の成分の分布を示すマッピングを図4に示す。図4より本発明例のアルミニウム系多孔質体はアルミニウム基地中にAl2O3(アルミナ)が分散することが確認された。Regarding the aluminum-based porous material of the present invention example, a scanning electron microscope (SEM) photograph of Al and O (oxygen) when the cross section of the skeleton is observed with an electron probe microanalyzer (EPMA). The mapping showing the distribution of the component of) is shown in FIG. From FIG. 4, it was confirmed that Al 2 O 3 (alumina) was dispersed in the aluminum base of the aluminum-based porous material of the present invention.
一方、比較例である試料番号03の多孔質試料の気孔状態を観察した写真を図5に示す。図5に示すように、比較例の多孔質試料は、アルミニウム粉末の一部で固相拡散により結合するのみであり、ネック部(粉末の結合部)が成長しておらず元の粉末の形状が確認できる。 On the other hand, the photograph which observed the pore state of the porous sample of the sample number 03 which is a comparative example is shown in FIG. As shown in FIG. 5, the porous sample of the comparative example is only bonded by solid phase diffusion in a part of the aluminum powder, and the neck portion (powder bonding portion) is not grown, and the shape of the original powder Can be confirmed.
また、試料番号04〜07のアルミニウム系多孔質体試料では、プラトー領域に達するまでに0.5MPa以上の弾性限界を示した。この弾性限界は、密度比の増加に伴って1.7MPaに達した。圧縮降伏試験の結果を、図6を参照して詳細に説明する。試料番号04の本発明例のアルミニウム系多孔質体試料では、変形初期に弾性変形してひずみ量の増加に従い応力が増加するが、その後は、ひずみ量が増加しても一定応力となっている。これは、アルミニウム系多孔質体試料の連通孔が圧縮されて潰されながら変形が進行している状態である。さらに荷重が増加してひずみ量が増加しアルミニウム系多孔質体試料が緻密化されると、通常の金属試料の場合と同様に荷重を増加するとひずみ量が増加するとともに応力が増加する傾向を示している。この変形挙動はアルミニウム系多孔質体試料の典型的な変形挙動である。試験後のアルミニウム系多孔質体試料を観察すると、連通孔は圧壊されているものの骨格の破断は確認されなかった。 In addition, the aluminum-based porous body samples of sample numbers 04 to 07 exhibited an elastic limit of 0.5 MPa or more before reaching the plateau region. This elastic limit reached 1.7 MPa with increasing density ratio. The result of the compression yield test will be described in detail with reference to FIG. In the aluminum-based porous material sample of sample number 04 of the present invention, the elastic deformation occurs at the initial stage of deformation and the stress increases as the amount of strain increases. Thereafter, the stress is constant even when the amount of strain increases. . This is a state in which deformation is proceeding while the communication hole of the aluminum-based porous material sample is compressed and crushed. When the load increases and the amount of strain increases and the aluminum-based porous material sample is densified, the amount of strain increases and the stress increases as the load increases as in the case of normal metal samples. ing. This deformation behavior is a typical deformation behavior of an aluminum based porous material sample. When the aluminum-based porous material sample after the test was observed, the rupture of the skeleton was not confirmed although the communication hole was crushed.
これに対して、試料番号01〜03のアルミニウム系多孔質体試料では、プラトー領域が存在しなかった。図6に示すように、試料番号03の比較例のアルミニウム系多孔質体試料では、粉末間の結合が不十分であることから、圧縮荷重を付加すると変形初期で破壊されており、試験後の試料はばらばらの粉末状態であった。 On the other hand, the plateau region did not exist in the aluminum-based porous material samples of sample numbers 01 to 03. As shown in FIG. 6, in the aluminum-based porous body sample of the comparative example of sample number 03, since the bonding between the powders is insufficient, it is destroyed at the initial stage of deformation when a compression load is applied. The sample was in a loose powder state.
以上より、荷重を加えた際にひずみ量の増加に従って応力量が増加した後、骨格の圧壊に伴って応力がほぼ横ばいとなり、その後応力が増加する応力−ひずみ線図を示す本発明のアルミニウム系多孔質体試料は、従来のアルミニウム系多孔質体試料よりも高い強度を有することが確認された。 From the above, the aluminum system of the present invention shows a stress-strain diagram in which stress increases substantially as the skeleton collapses after the stress increases as the strain increases when a load is applied, and the stress increases thereafter. It was confirmed that the porous body sample has higher strength than the conventional aluminum-based porous body sample.
本発明のアルミニウム系多孔質体は、高い強度を示すことから各種多孔質部材に用いて好適である。 Since the aluminum-based porous body of the present invention exhibits high strength, it is suitable for use in various porous members.
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