JP6655588B2 - Method of manufacturing aluminum-based composite material, aluminum-based composite material manufactured by the method, and aluminum-based structure including aluminum-based composite material - Google Patents
Method of manufacturing aluminum-based composite material, aluminum-based composite material manufactured by the method, and aluminum-based structure including aluminum-based composite material Download PDFInfo
- Publication number
- JP6655588B2 JP6655588B2 JP2017215334A JP2017215334A JP6655588B2 JP 6655588 B2 JP6655588 B2 JP 6655588B2 JP 2017215334 A JP2017215334 A JP 2017215334A JP 2017215334 A JP2017215334 A JP 2017215334A JP 6655588 B2 JP6655588 B2 JP 6655588B2
- Authority
- JP
- Japan
- Prior art keywords
- aluminum
- composite material
- based composite
- present
- carbide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/60—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using solids, e.g. powders, pastes
- C23C8/62—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using solids, e.g. powders, pastes only one element being applied
- C23C8/68—Boronising
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C24/00—Coating starting from inorganic powder
- C23C24/08—Coating starting from inorganic powder by application of heat or pressure and heat
- C23C24/10—Coating starting from inorganic powder by application of heat or pressure and heat with intermediate formation of a liquid phase in the layer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
- Y10T428/12764—Next to Al-base component
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Laminated Bodies (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Description
本発明は、アルミニウム基複合材料の製造方法、当該方法により製造されたアルミニウム基複合材料、及びアルミニウム基複合材料を含むアルミニウム基構造に関する。 The present invention relates to a method for manufacturing an aluminum-based composite material, an aluminum-based composite material manufactured by the method, and an aluminum-based structure including the aluminum-based composite material.
金属基複合材料(Metal Matrix Composite、MMC)は、金属材料を基材とし、特別なプロセスにより、種類の異なる、形態の異なるセラミック、非金属強化相を、連続する金属基材内に均一に分布させた新規複合材料である。その性能は、金属基材と強化相の利点を兼ね備え、高い比強度及び比剛性を有し、高温に耐えられ、摩耗に耐えられ、横性能及び層間せん断強度が高く、かつ高い熱的安定性、体積安定性及び材料の設計可能性を有するので、真っ先に航空宇宙産業に適用される。 Metal Matrix Composites (MMCs) are based on metal materials and use special processes to uniformly distribute different types, different forms of ceramics and non-metal reinforced phases in a continuous metal substrate. It is a new composite material. Its performance combines the advantages of a metal substrate and a reinforcing phase, has high specific strength and specific rigidity, can withstand high temperatures, withstand abrasion, has high lateral performance and interlaminar shear strength, and has high thermal stability Because of its volume stability and material design possibilities, it is first applied to the aerospace industry.
現在、金属基複合材料は、例えば次の問題があるので、量産及び商業化が困難となる。1、金属基材が十分な流動性を有し、強化相の間の隙間に十分に浸透してそれと複合することを確保するために、高温で行う必要があり、しかしながら、高温で強化相と基材とは有害な界面反応が発生することがある。2、金属基材と強化相との間の相溶性が悪い。3、強化相が設計要求における含有量、方向で基材内に均一に分布していることを確保しなければならない。 At present, mass-production and commercialization of metal-based composite materials are difficult, for example, because of the following problems. 1.It must be performed at high temperature to ensure that the metal substrate has sufficient fluidity and penetrates well into the gaps between the strengthening phases and composites with it, however, Harmful interfacial reactions may occur with the substrate. 2. Poor compatibility between the metal substrate and the reinforcing phase. 3. It must be ensured that the reinforcing phase is uniformly distributed in the base material in the content and direction according to the design requirements.
本発明の主な目的は、アルミニウム基金属を、好ましい機械的強度を有するアルミニウム基金属複合材料に製造することができるアルミニウム基複合材料の製造方法を提供することにある。 A main object of the present invention is to provide a method for producing an aluminum-based composite material that can produce an aluminum-based metal into an aluminum-based metal composite material having favorable mechanical strength.
本発明の別の目的は、好ましい機械的強度を有するアルミニウム基複合材料を提供することにある。 Another object of the present invention is to provide an aluminum-based composite material having favorable mechanical strength.
本発明の別の目的は、好ましい機械的強度を有するアルミニウム基構造を提供することにある。 It is another object of the present invention to provide an aluminum-based structure having favorable mechanical strength.
本発明のアルミニウム基金属の処理方法は、ホウ砂でアルミニウム基金属の表面を覆い、アルミニウム基金属をホウ砂の融点を超えるように加熱することである。 In the method for treating an aluminum-based metal according to the present invention, the surface of the aluminum-based metal is covered with borax, and the aluminum-based metal is heated so as to exceed the melting point of the borax.
本発明の一実施例において、アルミニウム基金属は、アルミニウム金属である。 In one embodiment of the present invention, the aluminum-based metal is an aluminum metal.
本発明の一実施例において、アルミニウム基金属は、アルミ合金である。 In one embodiment of the present invention, the aluminum-based metal is an aluminum alloy.
本発明の一実施例において、ホウ砂をセラミック材料と混合してから、アルミニウム基金属の表面を覆い、アルミニウム基金属を、ホウ砂の融点を超えるように加熱し、当該ホウ砂に対するセラミック材料の含有量は、0.01〜90wt%である。 In one embodiment of the present invention, the borax is mixed with the ceramic material, and then the surface of the aluminum-based metal is covered, and the aluminum-based metal is heated so as to exceed the melting point of the borax. The content is 0.01 to 90 wt%.
本発明の一実施例において、セラミック材料の硬度は、アルミニウムの硬度よりも大きい。 In one embodiment of the present invention, the hardness of the ceramic material is greater than the hardness of aluminum.
本発明の一実施例において、セラミック材料は、炭化シリコン(Silicon carbide)、タングステンカーバイド(Tungsten carbide)、炭化ホウ素(Boron carbide)、炭化ジルコニウム(Zirconium carbide)、炭化チタン(Titanium carbide)、炭化ベリリウム(Beryllium carbide)、ホウ化ジルコニウム(Zirconium boride)、二ホウ化チタン(Titanium diboride)、二ホウ化レニウム(Rhenium diboride)、ホウ化アルミニウム(Aluminum boride)、酸化アルミニウム(Aluminium oxide)、窒化ホウ素(Boron nitride)、ダイヤモンド、及びこれらの組合せからなる群から選ばれる。 In one embodiment of the present invention, the ceramic material is silicon carbide, tungsten carbide, boron carbide, zirconium carbide, titanium carbide, beryllium carbide. Beryllium carbide, Zirconium boride, Titanium diboride, Rhenium diboride, Rhenium diboride, Aluminum boride, Aluminum oxide, Boron nitride ), Diamond, and combinations thereof.
本発明のアルミニウム基複合材料は、7〜9atomic%のアルミニウムと、11〜13atomic%のナトリウムと、79〜81atomic%の酸素とを含む。 The aluminum-based composite material of the present invention contains 7 to 9 atomic% of aluminum, 11 to 13 atomic% of sodium, and 79 to 81 atomic% of oxygen.
本発明の一実施例において、アルミニウム基複合材料は、8atomic%のアルミニウムと、12atomic%のナトリウムと、80atomic%の酸素とを含む。 In one embodiment of the present invention, the aluminum-based composite material includes 8 atomic% aluminum, 12 atomic% sodium, and 80 atomic% oxygen.
本発明の一実施例において、アルミニウム基複合材料は、セラミック材料をさらに含み、アルミニウム基複合材料におけるアルミニウムの含有量が2〜3wt%であり、ナトリウムの含有量が3.5〜5wt%であり、酸素の含有量が26〜27wt%であり、セラミック材料の含有量が65〜68wt%である。 In one embodiment of the present invention, the aluminum-based composite further includes a ceramic material, wherein the aluminum-based composite has an aluminum content of 2 to 3 wt%, a sodium content of 3.5 to 5 wt%, and oxygen. Is 26 to 27% by weight, and the content of the ceramic material is 65 to 68% by weight.
本発明の一実施例において、セラミック材料の硬度は、アルミニウムの硬度よりも大きい。 In one embodiment of the present invention, the hardness of the ceramic material is greater than the hardness of aluminum.
本発明の一実施例において、セラミック材料は、炭化シリコン(Silicon carbide)、タングステンカーバイド(Tungsten carbide)、炭化ホウ素(Boron carbide)、炭化ジルコニウム(Zirconium carbide)、炭化チタン(Titanium carbide)、炭化ベリリウム(Beryllium carbide)、ホウ化ジルコニウム(Zirconium boride)、二ホウ化チタン(Titanium diboride)、二ホウ化レニウム(Rhenium diboride)、ホウ化アルミニウム(Aluminum boride)、酸化アルミニウム(Aluminium oxide)、窒化ホウ素(Boron nitride)、ダイヤモンド、及びこれらの組合せからなる群から選ばれる。 In one embodiment of the present invention, the ceramic material is silicon carbide, tungsten carbide, boron carbide, zirconium carbide, titanium carbide, beryllium carbide. Beryllium carbide, Zirconium boride, Titanium diboride, Rhenium diboride, Rhenium diboride, Aluminum boride, Aluminum oxide, Boron nitride ), Diamond, and combinations thereof.
本発明のアルミニウム基構造は、アルミニウム基金属で構成されるアルミニウム基基材と、アルミニウム基基材内に設けられているアルミニウム基複合材料とを含む。アルミニウム基複合材料は、7〜9atomic%のアルミニウムと、11〜13atomic%のナトリウムと、79〜81atomic%の酸素とを含む。 The aluminum-based structure of the present invention includes an aluminum-based substrate made of an aluminum-based metal and an aluminum-based composite material provided in the aluminum-based substrate. The aluminum-based composite material contains 7-9 atomic% of aluminum, 11-13 atomic% of sodium, and 79-81 atomic% of oxygen.
本発明の一実施例において、アルミニウム基複合材料は、8atomic%のアルミニウムと、12atomic%のナトリウムと、80atomic%の酸素とを含む。 In one embodiment of the present invention, the aluminum-based composite material includes 8 atomic% aluminum, 12 atomic% sodium, and 80 atomic% oxygen.
本発明の一実施例において、アルミニウム基複合材料は、セラミック材料をさらに含み、アルミニウム基複合材料におけるアルミニウムの含有量が2〜3wt%であり、ナトリウムの含有量が3.5〜5wt%であり、酸素の含有量が26〜27wt%であり、セラミック材料の含有量が65〜68wt%である。 In one embodiment of the present invention, the aluminum-based composite further includes a ceramic material, wherein the aluminum-based composite has an aluminum content of 2 to 3 wt%, a sodium content of 3.5 to 5 wt%, and oxygen. Is 26 to 27% by weight, and the content of the ceramic material is 65 to 68% by weight.
本発明の一実施例において、セラミック材料の硬度は、アルミニウムの硬度よりも大きい。 In one embodiment of the present invention, the hardness of the ceramic material is greater than the hardness of aluminum.
本発明の一実施例において、セラミック材料は、炭化シリコン(Silicon carbide)、タングステンカーバイド(Tungsten carbide)、炭化ホウ素(Boron carbide)、炭化ジルコニウム(Zirconium carbide)、炭化チタン(Titanium carbide)、炭化ベリリウム(Beryllium carbide)、ホウ化ジルコニウム(Zirconium boride)、二ホウ化チタン(Titanium diboride)、二ホウ化レニウム(Rhenium diboride)、ホウ化アルミニウム(Aluminum boride)、酸化アルミニウム(Aluminium oxide)、窒化ホウ素(Boron nitride)、ダイヤモンド、及びこれらの組合せからなる群から選ばれる。 In one embodiment of the present invention, the ceramic material is silicon carbide, tungsten carbide, boron carbide, zirconium carbide, titanium carbide, beryllium carbide. Beryllium carbide, Zirconium boride, Titanium diboride, Rhenium diboride, Rhenium diboride, Aluminum boride, Aluminum oxide, Boron nitride ), Diamond, and combinations thereof.
本発明のアルミニウム基複合材料の製造方法は、ホウ砂でアルミニウム基金属の表面を覆い、アルミニウム基金属をホウ砂の融点を超えるように加熱することである。そのうち、ホウ砂の融点は743℃である。そのうち、アルミニウム基金属は、アルミニウム金属、あるいはアルミ合金であってよい。 In the method for producing an aluminum-based composite material of the present invention, the surface of the aluminum-based metal is covered with borax, and the aluminum-based metal is heated so as to exceed the melting point of the borax. The melting point of borax is 743 ° C. Among them, the aluminum-based metal may be an aluminum metal or an aluminum alloy.
より具体的には、ホウ砂を、アルミニウム、アルミ合金又は/及びこれらの組合せで構成されるアルミニウム基金属に平坦に敷き、例えば高温炉内の高温環境に置いて743℃を超えるように加熱することにより、ホウ砂とアルミニウムを反応させて強化相を形成する。反応の過程において、不活性ガス(例えばアルゴン)による保護の有無にかかわらず、反応が進行できる。換言すれば、以上の本発明のアルミニウム基金属の処理方法は、酸素が存在する環境下で行うことができる。 More specifically, borax is spread flat on an aluminum base metal composed of aluminum, an aluminum alloy or / and a combination thereof, and is heated, for example, in a high temperature environment of a high temperature furnace to exceed 743 ° C. Thereby, borax and aluminum react to form a strengthening phase. In the course of the reaction, the reaction can proceed with or without protection by an inert gas (eg, argon). In other words, the above-described method for treating an aluminum-based metal of the present invention can be performed in an environment where oxygen is present.
別の角度から見れば、上記のアルミニウム基複合材料の製造方法は、実質的にアルミニウム基金属の処理方法である。図1に示す光学顕微鏡による写真(VHX-5000、Keyence社、アメリカ)において、明るい領域は本発明の方法で処理されていないアルミニウムであり、暗い領域は本発明の方法で処理されたアルミニウムである。そのうち、図面における明るい領域のうちの数字1、2、3、4で示す箇所及び暗い領域のうちの数字5、6、7、8で示す箇所について、ナノインデンター(Nanoindenters)(Nanoindenter XP、MTS社、アメリカ)を使用して、硬度及びヤング率の測定を行い、結果は下記の表1のとおりである。 From another angle, the above-described method for producing an aluminum-based composite material is substantially a method for treating an aluminum-based metal. In the light micrograph shown in FIG. 1 (VHX-5000, Keyence, USA), the bright areas are aluminum not treated by the method of the present invention, and the dark areas are aluminum treated by the method of the present invention. . Among them, the portions indicated by the numbers 1, 2, 3, and 4 in the bright region and the portions indicated by the numbers 5, 6, 7, and 8 in the dark region in the drawing are Nanoindenters (Nanoindenter XP, MTS). , USA), and the hardness and Young's modulus were measured, and the results are as shown in Table 1 below.
表1から分かるように、本発明の方法で処理されたアルミニウムの機械的強度は、明らかに本発明の方法で処理されていないアルミニウムよりも優れた。より具体的には、本発明の方法で処理されたアルミニウムでは、数字5、6、7、8で示す箇所におけるベルコヴィッチ硬度の平均値が4.59Gpa((4.13+4.33+5.01+4.89)/4=4.59)であり、ヤング率の平均値が126.98Gpa((124.4+122.2+132.8+128.5)/4=126.98)である。それに対して、本発明の方法で処理されていないアルミニウムでは、数字1、2、3、4で示す箇所におけるベルコヴィッチ硬度の平均値が0.6Gpa((0.534+0.677+0.655+0.534)/4=0.6)であり、ヤング率の平均値が75.2Gpa((71.42+79.19+73.35+76.84)/4=75.2)である。即ち、本発明の方法で処理された後に、アルミニウムのベルコヴィッチ硬度及びヤング率は、それぞれ元の値の7.65倍及び1.68倍まで向上した。 As can be seen from Table 1, the mechanical strength of the aluminum treated by the method of the present invention was clearly superior to aluminum not treated by the method of the present invention. More specifically, the aluminum treated by the method of the present invention has an average Berkovich hardness of 4.59 Gpa ((4.13 + 4.33 + 5.01 + 4.89) /) at the locations indicated by the numerals 5, 6, 7, and 8. 4 = 4.59), and the average value of the Young's modulus is 126.98 Gpa ((124.4 + 122.2 + 132.8 + 128.5) /4=126.98). On the other hand, in the aluminum not treated by the method of the present invention, the average value of the Berkovich hardness at the locations indicated by the numerals 1, 2, 3, and 4 is 0.6 GPa ((0.534 + 0.677 + 0.655 + 0.534) / 4). = 0.6), and the average value of the Young's modulus is 75.2 GPa ((71.42 + 79.19 + 73.35 + 76.84) /4=75.2). That is, after being treated with the method of the present invention, the Berkovich hardness and Young's modulus of aluminum have been increased to 7.65 times and 1.68 times the original values, respectively.
5083アルミ合金についても、前記ベルコヴィッチ硬度及びヤング率の測定を行い、その結果を表2に示す。 The Berkovich hardness and Young's modulus of the 5083 aluminum alloy were also measured, and the results are shown in Table 2.
表2から分かるように、本発明の方法で処理された5083アルミ合金の機械的強度は、明らかに本発明の方法で処理されていない5083アルミ合金よりも優れた。より具体的には、本発明の方法で処理された5083アルミ合金では、数字5、6、7、8で示す箇所におけるベルコヴィッチ硬度の平均値が5.02Gpa((4.87+5.22+4.98+5.01)/4=5.02)であり、ヤング率の平均値が126.2Gpa((125.8+131.4+121.5+126.1)/4=126.2)である。それに対して、本発明の方法で処理されていないアルミニウムでは、数字1、2、3、4で示す箇所におけるベルコヴィッチ硬度の平均値が1.08Gpa((1.081+1.121+0.983+1.122)/4=1.08)であり、ヤング率の平均値が71.96Gpa((72.33+71.88+73.54+70.09)/4=71.95)である。即ち、本発明の方法で処理された後に、5083アルミ合金のベルコヴィッチ硬度及びヤング率は、それぞれ元の値の4.65倍及び1.37倍まで向上した。 As can be seen from Table 2, the mechanical strength of the 5083 aluminum alloy treated by the method of the present invention was clearly superior to the 5083 aluminum alloy not treated by the method of the present invention. More specifically, in the 5083 aluminum alloy treated by the method of the present invention, the average value of the Berkovich hardness at the locations indicated by the numerals 5, 6, 7, and 8 is 5.02 GPa ((4.87 + 5.22 + 4.98 + 5.01 Gpa). ) / 4 = 5.02), and the average value of the Young's modulus is 126.2 GPa ((125.8 + 131.4 + 121.5 + 126.1) / 4 = 126.2). On the other hand, in the aluminum not treated by the method of the present invention, the average value of the Berkovich hardness at the locations indicated by the numerals 1, 2, 3, and 4 is 1.08 GPa ((1.081 + 1.121 + 1.983 + 1.122) / 4. = 1.08), and the average Young's modulus is 71.96 Gpa ((72.33 + 71.88 + 73.54 + 70.09) / 4 = 71.95). That is, after being treated by the method of the present invention, the Berkovich hardness and Young's modulus of the 5083 aluminum alloy were improved to 4.65 times and 1.37 times the original values, respectively.
これによって、本発明の方法によれば、アルミニウム基金属を、高い機械的強度を有するアルミニウム基複合材料に製造することができる。あるいは、別の角度から見れば、アルミニウム基金属の機械的強度を向上させることができる。 Thus, according to the method of the present invention, an aluminum-based metal can be manufactured into an aluminum-based composite material having high mechanical strength. Alternatively, from another angle, the mechanical strength of the aluminum-based metal can be improved.
他方、本発明の方法で処理されたアルミニウム基金属と本発明の方法で処理されていないアルミニウム基金属との間は、良好な相溶性を有する。さらには、図2に示す光学顕微鏡による写真図には、本発明の方法で処理されたアルミニウムの横断面を示す。この図から、本発明の方法で処理されたアルミニウムと本発明の方法で処理されていないアルミニウムは互いに隙間なく接続することが見られ、それらは、良好な相溶性を有し、かつ界面結合が良好であることが分かる。 On the other hand, there is good compatibility between the aluminum-based metal treated by the method of the present invention and the aluminum-based metal not treated by the method of the present invention. Further, a photographic view by an optical microscope shown in FIG. 2 shows a cross section of aluminum treated by the method of the present invention. From this figure it can be seen that the aluminum treated by the method of the invention and the aluminum not treated by the method of the invention are connected to each other without gaps, they have good compatibility, and the interfacial bonding is It turns out that it is good.
図3に示すような走査型電子顕微鏡による画像(Nova 230 Variable Pressure SEM (VP-SEM) (at 10 kV accelerating voltage)、FEI社、アメリカ)において、暗い領域は本発明の方法で処理されていないアルミニウムであり、明るい領域は本発明の方法で処理されたアルミニウムである。明るい領域に対して元素分析を行ったところ、図4A〜4Cに示す結果が得られた。そのうち、それぞれ図4A、4B及び4Cから、明るい領域は約8atomic%のアルミニウムと、約12atomic%のナトリウムと、約80atomic%の酸素とを含むことが分かる。さらには、本発明の方法で処理されたアルミニウム基金属は、好ましい機械的強度を有するアルミニウム基複合材料である。そのうち、アルミニウム基複合材料は、7〜9atomic%のアルミニウムと、11〜13atomic%のナトリウムと、79〜81atomic%の酸素とを含み、好ましくは、約8atomic%のアルミニウムと、約12atomic%のナトリウムと、約80atomic%の酸素とを含む。 In a scanning electron microscope image as shown in FIG. 3 (Nova 230 Variable Pressure SEM (VP-SEM) (at 10 kV accelerating voltage), FEI, USA), dark areas are not treated by the method of the present invention. Aluminum, and the bright areas are aluminum treated by the method of the present invention. When the elemental analysis was performed on the bright region, the results shown in FIGS. 4A to 4C were obtained. 4A, 4B, and 4C, respectively, that the bright region contains about 8 atomic% of aluminum, about 12 atomic% of sodium, and about 80 atomic% of oxygen. Furthermore, the aluminum-based metal treated by the method of the present invention is an aluminum-based composite material having favorable mechanical strength. Among them, the aluminum-based composite material contains 7 to 9 atomic% of aluminum, 11 to 13 atomic% of sodium, and 79 to 81 atomic% of oxygen, preferably, about 8 atomic% of aluminum and about 12 atomic% of sodium. Contains about 80 atomic% oxygen.
図4Dに示すような走査型電子顕微鏡による画像(Nova 230 Variable Pressure SEM (VP-SEM) (at 10 kV accelerating voltage)、FEI社、アメリカ)において、暗い領域は本発明の方法で処理されていない5083アルミ合金であり、明るい領域は本発明の方法で処理された5083アルミ合金である。明るい領域に対して元素分析を行ったところ、図4E〜4Hに示すような結果が得られた。そのうち、それぞれ図4E、4F、4G及び4Hから、明るい領域は約12atomic%のナトリウムと、約8atomic%のマグネシウムと、約7atomic%のアルミニウムと、約73atomic%の酸素とを含むことが分かる。 In a scanning electron microscope image (Nova 230 Variable Pressure SEM (VP-SEM) (at 10 kV accelerating voltage), FEI, USA) as shown in FIG. 4D, dark areas are not treated by the method of the present invention. 5083 aluminum alloy, and the bright area is 5083 aluminum alloy treated by the method of the present invention. When the elemental analysis was performed on the bright region, the results shown in FIGS. 4E to 4H were obtained. 4E, 4F, 4G, and 4H, respectively, reveal that the bright region contains about 12 atomic% of sodium, about 8 atomic% of magnesium, about 7 atomic% of aluminum, and about 73 atomic% of oxygen.
別の実施例において、ホウ砂をセラミック材料と混合してから、アルミニウム基金属の表面を覆い、743℃を超えるように加熱する。より具体的には、例えば硬度及びヤング率などの機械的強度をさらに向上させるために、ホウ砂に強度のより高い(例えば硬度がアルミニウムよりも高い)セラミック材料を混合することができる。そのうち、セラミック材料は、炭化シリコン(Silicon carbide)、タングステンカーバイド(Tungsten carbide)、炭化ホウ素(Boron carbide)、炭化ジルコニウム(Zirconium carbide)、炭化チタン(Titanium carbide)、炭化ベリリウム(Beryllium carbide)、ホウ化ジルコニウム(Zirconium boride)、二ホウ化チタン(Titanium diboride)、二ホウ化レニウム(Rhenium diboride)、ホウ化アルミニウム(Aluminum boride)、酸化アルミニウム(Aluminium oxide)、窒化ホウ素(Boron nitride)、ダイヤモンド、及びこれらの組合せからなる群から選ばれることが好ましい。セラミック材料の含有量は、ホウ砂に対して0.01〜90wt%であり、好ましくは、66wt%のセラミック材料:33%のホウ砂である。 In another embodiment, the borax is mixed with the ceramic material and then coated over the aluminum-based metal and heated to above 743 ° C. More specifically, a higher strength ceramic material (eg, having a higher hardness than aluminum) can be mixed with borax to further improve mechanical strength such as, for example, hardness and Young's modulus. Among them, ceramic materials include silicon carbide, silicon carbide, tungsten carbide, boron carbide, zirconium carbide, titanium carbide, beryllium carbide, and boride. Zirconium (Zirconium boride), titanium diboride (Titanium diboride), rhenium diboride (Rhenium diboride), aluminum boride (Aluminum boride), aluminum oxide (Aluminium oxide), boron nitride (Boron nitride), diamond, and these Is preferably selected from the group consisting of: The content of the ceramic material is 0.01 to 90 wt% with respect to the borax, preferably 66 wt% ceramic material: 33% borax.
一実施例において、ホウ砂をまず炭化シリコンと混合し、比率は、66wt%の炭化シリコン:33%のホウ砂である。その後、その混合物でアルミ合金の表面を覆い、743℃を超えるように加熱する。図5Aに示すような光学顕微鏡による写真(VHX-5000、Keyence社、アメリカ)において、明るい領域は炭化シリコンであり、暗い領域はホウ砂とアルミニウムとが反応して生成した強化相である。全体に対して機械的強度の測定を行ったところ、その硬度は9.7GPaであり、ヤング率は140GPaであることが分かる。上述したことから分かるように、本発明の方法により、例えば炭化シリコンなどの高強度のセラミック材料をアルミニウム相に侵入させることで、アルミニウム基金属を強化する効果に達することができる。別の実施例における、炭化シリコンが5083アルミ合金複合材料内にある場合、タングステンカーバイドがアルミニウム複合材料内にある場合、炭化チタンが5083アルミ合金複合材料内にある場合、酸化チタンがアルミニウム複合材料内にある場合、及び酸化チタンが5083アルミ合金複合材料内にある場合の光学顕微鏡による写真は、それぞれ図5B〜5Fに示す。 In one embodiment, borax is first mixed with silicon carbide, the ratio being 66 wt% silicon carbide: 33% borax. Thereafter, the surface of the aluminum alloy is covered with the mixture, and the mixture is heated to exceed 743 ° C. In the light micrograph (VHX-5000, Keyence, USA) as shown in FIG. 5A, the bright region is silicon carbide and the dark region is the strengthening phase formed by the reaction between borax and aluminum. When the mechanical strength of the whole was measured, it was found that the hardness was 9.7 GPa and the Young's modulus was 140 GPa. As can be seen from the foregoing, the method of the present invention can achieve the effect of strengthening the aluminum-based metal by infiltrating a high-strength ceramic material, such as silicon carbide, into the aluminum phase. In another embodiment, when silicon carbide is in the 5083 aluminum alloy composite, when tungsten carbide is in the aluminum composite, when titanium carbide is in the 5083 aluminum alloy composite, titanium oxide is in the aluminum composite. And the titanium oxide in the 5083 aluminum alloy composite is shown in FIGS. 5B-5F, respectively.
さらには、ホウ砂を、セラミック材料と混合してから、アルミニウム基金属の表面を覆い、743℃を超えるように加熱することで、好ましい機械的強度を有する、セラミック材料を含むアルミニウム基複合材料を得ることができる。そのうち、セラミック材料は、炭化シリコン(Silicon carbide)、タングステンカーバイド(Tungsten carbide)、炭化ホウ素(Boron carbide)、炭化ジルコニウム(Zirconium carbide)、炭化チタン(Titanium carbide)、炭化ベリリウム(Beryllium carbide)、ホウ化ジルコニウム(Zirconium boride)、二ホウ化チタン(Titanium diboride)、二ホウ化レニウム(Rhenium diboride)、ホウ化アルミニウム(Aluminum boride)、酸化アルミニウム(Aluminium oxide)、酸化チタン(Titanium oxide)、窒化ホウ素(Boron nitride)、ダイヤモンド、及びこれらの組合せからなる群から選ばれることが好ましい。セラミック材料の含有量は、ホウ砂に対して0.01〜90wt%であり、好ましくは、66wt%のセラミック材料:33%のホウ砂である。 Furthermore, by mixing borax with a ceramic material, and then covering the surface of the aluminum-based metal and heating it to exceed 743 ° C., an aluminum-based composite material containing a ceramic material having favorable mechanical strength is obtained. Obtainable. Among them, ceramic materials include silicon carbide, silicon carbide, tungsten carbide, boron carbide, zirconium carbide, titanium carbide, beryllium carbide, and boride. Zirconium (Zirconium boride), titanium diboride (Titanium diboride), rhenium diboride (Rhenium diboride), aluminum boride (Aluminum boride), aluminum oxide (Aluminium oxide), titanium oxide (Titanium oxide), boron nitride (Boron) nitride, diamond, and combinations thereof. The content of the ceramic material is 0.01 to 90 wt% with respect to the borax, preferably 66 wt% ceramic material: 33% borax.
前記アルミニウム基複合材料は、アルミニウム基基材に埋め込まれてアルミニウム基構造を形成することができる。より具体的には、アルミニウム基構造は、アルミニウム基金属で構成されるアルミニウム基基材と、アルミニウム基基材内に設けられているアルミニウム基複合材料とを含む。換言すれば、アルミニウム基金属で構成されるアルミニウム基基材が多層式強化構造を挟んでいる。図6に示す実施例において、アルミニウム基構造は、単層のアルミニウム基複合材料を有し、アルミニウム基複合材料が、二つのアルミニウム金属層の間に挟設されている。しかしながら、別の実施例において、アルミニウム基構造は、単層のアルミニウム基複合材料のみを有することに限らず、アルミニウム基複合材料は、二つのアルミニウム金属層の間に挟設されていることに限らない。 The aluminum-based composite material can be embedded in an aluminum-based substrate to form an aluminum-based structure. More specifically, the aluminum-based structure includes an aluminum-based substrate made of an aluminum-based metal and an aluminum-based composite material provided in the aluminum-based substrate. In other words, an aluminum-based substrate made of an aluminum-based metal sandwiches the multilayer reinforced structure. In the embodiment shown in FIG. 6, the aluminum-based structure has a single-layer aluminum-based composite material, and the aluminum-based composite material is sandwiched between two aluminum metal layers. However, in another embodiment, the aluminum-based structure is not limited to having only a single layer of aluminum-based composite material, and the aluminum-based composite material is not limited to being sandwiched between two aluminum metal layers. Absent.
アルミニウム金属(No layer)、単層のアルミニウム基複合材料を有するアルミニウム基構造(1 layer)及び4層のアルミニウム基複合材料を有するアルミニウム基構造(4 layers)に対して3点曲げ試験を行ってその曲げ強度を評価する。そのうち、曲げ試験は、曲げ強度試験機(Instron 5900、Instron社、アメリカ)を使用して行われ、条件は、押し下げ速度が3×10-4in/秒であり、両点の間隔が6mmである。結果は図7に示すとおりである。図7から分かるように、4層のアルミニウム基複合材料を有するアルミニウム基構造の曲げ強度は、明らかにアルミニウム金属の曲げ強度よりも大きく、単層のアルミニウム基複合材料を有するアルミニウム基構造の曲げ強度も、アルミニウム金属の曲げ強度よりも僅かに大きい。これによって、本発明のアルミニウム基構造は、アルミニウム金属に比べ、好ましい強度を有する。 A three-point bending test was performed on aluminum metal (No layer), an aluminum-based structure with a single layer of aluminum-based composite (1 layer), and an aluminum-based structure with 4 layers of aluminum-based composite (4 layers). The bending strength is evaluated. Among them, bending test, flexural strength tester (Instron 5900, Instron Corp., USA) were performed using, conditions, depress the rate is 3 × 10 -4 in / sec, at intervals of both points are 6mm is there. The results are as shown in FIG. As can be seen from FIG. 7, the bending strength of the aluminum-based structure having the four-layer aluminum-based composite material is clearly greater than the bending strength of the aluminum metal, and the bending strength of the aluminum-based structure having the single-layer aluminum-based composite material is shown. Is also slightly greater than the bending strength of aluminum metal. As a result, the aluminum-based structure of the present invention has preferable strength as compared with aluminum metal.
前記の説明及び図面により既に本発明の好ましい実施例を開示したが、各種の追加、多くの修正及び置換が本発明の好ましい実施例に使用可能であり、添付の特許請求の範囲によって限定されるような本発明の原理の趣旨及び範囲を逸脱することがないことを理解しなければならない。本発明の属する技術の分野における通常の知識を有する者は、本発明が多くの形式、構造、配置、割合、材料、部品及びパッケージの修正に使用可能であることが分かる。したがって、本明細書に開示した実施例は、本発明を限定するためのものではなく、本発明を説明するためのものと見なされるべきである。本発明の範囲は以下の添付の特許請求の範囲によって限定されるべきであり、その合法的な均等物を含み、以上の説明に限らない。
Although the preferred embodiment of the present invention has been disclosed by the foregoing description and drawings, various additions, many modifications and substitutions can be used in the preferred embodiment of the present invention, and are limited by the appended claims. It is to be understood that such changes do not depart from the spirit and scope of the principles of the present invention. Those of ordinary skill in the art to which this invention pertains will appreciate that the invention can be used to modify many forms, structures, arrangements, proportions, materials, parts and packages. Therefore, the examples disclosed herein should not be considered as limiting the invention, but as illustrating the invention. The scope of the invention is to be limited by the appended claims, including their legal equivalents, and not by the foregoing description.
Claims (6)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15/348,367 | 2016-11-10 | ||
| US15/348,367 US20180127881A1 (en) | 2016-11-10 | 2016-11-10 | Process for producing aluminum-based metal composite, aluminum-based composite obtained by using the same, and aluminum-based structure having the aluminum-based composite |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2018090907A JP2018090907A (en) | 2018-06-14 |
| JP6655588B2 true JP6655588B2 (en) | 2020-02-26 |
Family
ID=62065482
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017215334A Expired - Fee Related JP6655588B2 (en) | 2016-11-10 | 2017-11-08 | Method of manufacturing aluminum-based composite material, aluminum-based composite material manufactured by the method, and aluminum-based structure including aluminum-based composite material |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20180127881A1 (en) |
| JP (1) | JP6655588B2 (en) |
| CN (1) | CN108070822A (en) |
| TW (1) | TWI680208B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109234562B (en) * | 2018-10-31 | 2020-12-18 | 江苏大学 | A method for regulating the preparation of in-situ binary nanoparticle-reinforced aluminum matrix composites |
| TWI837508B (en) * | 2021-09-07 | 2024-04-01 | 財團法人工業技術研究院 | Composite structure with aluminum-based alloy layer containg boroncarbide and manufacturing method thereof |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1817888A (en) * | 1927-09-15 | 1931-08-04 | Doherty Res Co | Protective coating (alborizing) |
| JPS6254588A (en) * | 1985-08-30 | 1987-03-10 | Toyota Motor Corp | Formation of composite aluminum alloy layer dispersed with ceramic particles |
| JPH068493B2 (en) * | 1986-04-22 | 1994-02-02 | 三菱電機株式会社 | Noble metal coating method |
| JPH02118083A (en) * | 1988-10-27 | 1990-05-02 | Toshiba Corp | Formation of ceramic layer on surface of metallic material |
| DE10314700A1 (en) * | 2003-03-31 | 2004-10-14 | Behr Gmbh & Co. Kg | Method for producing surface-modified workpieces |
| CN1293227C (en) * | 2004-10-29 | 2007-01-03 | 武汉理工大学 | Quick preparation method of metal surface boronizing layer |
| EP2058418A1 (en) * | 2007-11-09 | 2009-05-13 | Mustafa K. Ürgen | Method for boriding of coatings using high speed electrolytic process |
| JP2009299167A (en) * | 2008-06-17 | 2009-12-24 | Honda Motor Co Ltd | Forming method of aluminum-based composite layer, and manufacturing method of brake rotor |
| US20150336219A1 (en) * | 2011-01-13 | 2015-11-26 | Siemens Energy, Inc. | Composite materials and methods for laser manufacturing and repair of metals |
| EP3321383B1 (en) * | 2016-11-11 | 2019-09-04 | Yung-Ching Chang | Process for producing aluminum-based metal composite, aluminum-based composite obtained by using the same, and aluminum-based structure having the aluminum-based composite |
-
2016
- 2016-11-10 US US15/348,367 patent/US20180127881A1/en not_active Abandoned
-
2017
- 2017-03-31 TW TW106111248A patent/TWI680208B/en active
- 2017-04-13 CN CN201710248211.0A patent/CN108070822A/en not_active Withdrawn
- 2017-11-08 JP JP2017215334A patent/JP6655588B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20180127881A1 (en) | 2018-05-10 |
| CN108070822A (en) | 2018-05-25 |
| TWI680208B (en) | 2019-12-21 |
| TW201817916A (en) | 2018-05-16 |
| JP2018090907A (en) | 2018-06-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Xia et al. | Microstructure growth behavior and its evolution mechanism during laser additive manufacture of in-situ reinforced (TiB+ TiC)/Ti composite | |
| Guo et al. | Microstructure and mechanical properties of C/C composite/TC4 joint with inactive AgCu filler metal | |
| Ren et al. | Influence of MoSi2 on oxidation protective ability of TaB2-SiC coating in oxygen-containing environments within a broad temperature range | |
| Zhang et al. | Microstructure and brazing mechanism of porous Si3N4/Invar joint brazed with Ag-Cu-Ti/Cu/Ag-Cu multi-layered filler | |
| JP2528217B2 (en) | Composite ceramic body | |
| CN1082567C (en) | Method for forming metal matrix composite containing three-dimensionally inter-connected co-matices | |
| Kang et al. | Effect of molybdenum carbide intermediate layers on thermal properties of copper–diamond composites | |
| KR0134957B1 (en) | A method of modifying ceramic composite bodies by a post-treatment process and articles produced thereby | |
| PL158056B1 (en) | Metal matrix composite production method PL PL PL | |
| CN87101720A (en) | Prepare the method for self-supporting material and with the product of its manufacturing | |
| NO175851B (en) | ||
| CN1042497A (en) | Method for preparing macrocomposites and macrocomposites produced by the method | |
| CN108500263B (en) | Rapid forming method of bionic shell structure titanium-based composite material | |
| CN1082554C (en) | Method of modifying properties of metal matrix composite body | |
| JPH01294558A (en) | Production of self-support and composite material produced thereby | |
| NO176349B (en) | Method of forming composites with metal matrix having variable amount of filler | |
| TW201418191A (en) | Metal-carbon composite material, metal-carbon composite material manufacturing method, and sliding member | |
| JP6655588B2 (en) | Method of manufacturing aluminum-based composite material, aluminum-based composite material manufactured by the method, and aluminum-based structure including aluminum-based composite material | |
| JP5541735B2 (en) | How to make a refractory carbide layer on a C / C composite part | |
| JP2010526008A5 (en) | ||
| JP2016113696A (en) | Manufacturing method of aluminum matrix composite material and aluminum matrix composite material manufactured by the same | |
| CN1701052A (en) | Method for preparing composite component and cermet component | |
| Soltani et al. | Improving the interfacial reaction between cristobalite silica from rice husk and Al–Mg–Si by CVD-Si3N4 deposition | |
| Jimenez et al. | Joining of Cf/SiC ceramics to nimonic alloys | |
| Leon-Patiño et al. | Microstructure and shear strength of sintered Cu–Al2O3 composite joined to Cu using Ag–Cu and Cu–Zn filler alloys |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20171130 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20181113 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20181127 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20190227 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20190410 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20190917 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20191004 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20200121 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20200203 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 6655588 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |