WO2002027055A1 - Alliage amorphe et procede de preparation dudit alliage - Google Patents
Alliage amorphe et procede de preparation dudit alliage Download PDFInfo
- Publication number
- WO2002027055A1 WO2002027055A1 PCT/JP2000/006589 JP0006589W WO0227055A1 WO 2002027055 A1 WO2002027055 A1 WO 2002027055A1 JP 0006589 W JP0006589 W JP 0006589W WO 0227055 A1 WO0227055 A1 WO 0227055A1
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- WO
- WIPO (PCT)
- Prior art keywords
- alloy
- zrc
- particles
- dispersed
- amorphous alloy
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C45/00—Amorphous alloys
- C22C45/10—Amorphous alloys with molybdenum, tungsten, niobium, tantalum, titanium, or zirconium or Hf as the major constituent
Definitions
- the present invention relates to an amorphous alloy, and more particularly to an amorphous ZrC particle dispersed alloy.
- amorphous alloy composite materials containing a second phase such as ceramics and metals have been developed to date. It was reported for the first time in 980 that increased yield strength and delocalization of fracture due to the compounding of amorphous alloys. In other words, this means that the Ni 78 S ii 0 Bi 2 quenched ribbon in which micron-sized tungsten carbide particles are dispersed has high strength.
- ZrC zirconium carbide
- an object of the present invention is to produce a ZrC particle-dispersed amorphous alloy composite material having excellent mechanical properties at low cost. Disclosure of the invention
- the present invention provides a method for melting an alloy serving as a matrix, adding carbon particles and a Zr alloy to the alloy, and melting the alloy at a temperature equal to or higher than the melting point of the Zr alloy + 100 K or more.
- ZrC particles are produced by reacting Zr and C during melting to produce an alloy in which ZrC particles are uniformly dispersed. Is the law.
- a ZrC particle-dispersed amorphous alloy having a desired shape can be formed from an alloy having glass forming ability obtained by adjusting an alloy in which the ZrC particles are uniformly dispersed.
- the present invention also includes a child dispersed amorphous alloy.
- FIG. 1 is an optical micrograph of a cross section of a structural composite material made of the alloy according to the present invention.
- FIG. 2 is a graph of X-ray diffraction of a cross section of a structural composite material made of the alloy according to the present invention.
- FIG. 3 is a graph showing a differential scanning calorimetry curve of a structural composite material made of the alloy according to the present invention.
- FIG. 4 is a graph showing a stress-strain curve under compression test of an alloy in which ZrC particles are uniformly dispersed.
- FIG. 5 is a graph showing the maximum stress in a compression test with respect to the volume fraction of ZrC particles.
- FIG. 6 is a graph showing plastic strain in a compression test with respect to the volume fraction of ZrC particles.
- FIG. 7 is a graph showing a Young's modulus by a compression test with respect to a volume fraction of ZrC particles.
- a method for producing a ZrC particle-dispersed Zr-based amorphous alloy composite material using the present invention is as follows: adding carbon particles and a Zr pure metal or a Zr alloy to a matrix alloy; The alloy is melted at a temperature equal to or higher than the melting point of the alloy +100 K, and Zr and C are reacted during melting to form ZrC particles.
- a ZrC particle-dispersed amorphous alloy can be manufactured by preparing a mother alloy having glass forming ability in which ZrC particles are uniformly dispersed and adjusting the same.
- the size of the carbon particles used for the preparation is 100 micrometer or less, and the size of the ZrC particles is desirably 100 micrometer or less.
- the dispersion ratio of the particles is desirably 20% or less by volume.
- Zr metal has the highest reactivity to graphite and the generated zirconium carbide (ZrC) is the most stable. Only ZrC particles are generated as a dispersed phase. (3)
- the master alloy containing the ZrC particles is pulverized and charged into a quartz nozzle, which is subjected to high-frequency melting in a vacuum atmosphere of 10 ⁇ 4 1rr or less, and then to a melt temperature of 850 ° C or more.
- a quartz nozzle which is subjected to high-frequency melting in a vacuum atmosphere of 10 ⁇ 4 1rr or less, and then to a melt temperature of 850 ° C or more.
- a copper mold diameter 2 mm, height 5 Omm shape).
- FIG. 1 shows an optical micrograph of a cross section of the structural composite material produced as described above. From this photograph, it can be seen that particles of 10 ⁇ m or less are uniformly dispersed in the parent phase.
- Figure 2 shows an X-ray diffraction pattern of a cross section of a structural composite material containing 15 V o 1% (volume fraction) of dispersed particles. Since this is composed of five peaks indicating ZrC and a halo pattern indicating an amorphous structure, the obtained composite material has a matrix of Zr-A1-Ni-Cu amorphous alloy. It can be seen that the dispersion is ZrC particles and the graphite has disappeared.
- Figure 3 shows the differential scanning calorimetry (DSC) curve (temperature rise rate 0.67K si) of the ZrC particle-dispersed Zr-based amorphous alloy composite containing 15 vo 1% dispersed particles.
- DSC differential scanning calorimetry
- Fig. 5 to Fig. 7 show how the maximum stress (Fig. 5), plastic strain (Fig. 6) and Young's modulus (Fig. 7) change according to the change of the volume fraction of ZrC particles. . From these figures, it can be seen that when the volume fraction is 20% or less, the maximum stress and the Young's coefficient increase as the proportion of ZrC particles increases, and their performance increases.However, with respect to plastic strain, the volume fraction 10% There is a peak when.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
Abstract
L'invention concerne un procédé pour préparer un matériau composite d'alliage amorphe contenant des particules ZrC dispersées dans ledit matériau. Ce procédé consiste à ajouter à un alliage mère des particules de carbone et un métal pur Zr ou un alliage Zr, les dissoudre à une température supérieure au point de fusion du métal pur Zr ou de l'alliage Zr + 100 °K, faire réagir Zr avec C pour former des particules ZrC et produire l'alliage mère mentionné ci-dessus capable de former du verre présentant des particules ZrC dispersées uniformément. Des matériaux composites d'alliage amorphe contenant diverses quantités de particules ZrC dispersées dans lesdits matériaux et présentant des formes souhaitées peuvent être préparés. Ce procédé peut être utilisé pour préparer, pour un faible coût, un matériau composite d'alliage amorphe contenant des particules ZrC dispersées dans ledit matériau, lequel matériau présente une excellente résistance mécanique.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002530815A JPWO2002027055A1 (ja) | 2000-09-25 | 2000-09-25 | アモルファス合金及びその作製法 |
PCT/JP2000/006589 WO2002027055A1 (fr) | 2000-09-25 | 2000-09-25 | Alliage amorphe et procede de preparation dudit alliage |
TW089119986A TWI235770B (en) | 2000-09-25 | 2000-09-27 | Amorphous alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2000/006589 WO2002027055A1 (fr) | 2000-09-25 | 2000-09-25 | Alliage amorphe et procede de preparation dudit alliage |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002027055A1 true WO2002027055A1 (fr) | 2002-04-04 |
Family
ID=11736516
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2000/006589 WO2002027055A1 (fr) | 2000-09-25 | 2000-09-25 | Alliage amorphe et procede de preparation dudit alliage |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPWO2002027055A1 (fr) |
TW (1) | TWI235770B (fr) |
WO (1) | WO2002027055A1 (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007092103A (ja) * | 2005-09-27 | 2007-04-12 | Japan Science & Technology Agency | 延性を有するマグネシウム基金属ガラス合金−金属粒体複合材 |
JP2009510267A (ja) * | 2005-10-03 | 2009-03-12 | エーテーハー チューリヒ | バルク金属ガラス/グラファイト複合材料 |
CN102529191A (zh) * | 2011-12-15 | 2012-07-04 | 比亚迪股份有限公司 | 一种非晶合金制品及其制造方法 |
CN105316603A (zh) * | 2015-10-26 | 2016-02-10 | 宋佳 | 一种高韧性非晶合金及其制备方法 |
CN105316604A (zh) * | 2015-10-26 | 2016-02-10 | 宋佳 | 一种高硬度非晶合金及其制备方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6475641A (en) * | 1987-09-18 | 1989-03-22 | Takeshi Masumoto | Amorphous alloy containing carbon grain and its manufacture |
JPH0688154A (ja) * | 1992-09-04 | 1994-03-29 | Mitsubishi Kasei Corp | 金属組成物及び発泡金属組成物の製造方法 |
JPH07157834A (ja) * | 1993-12-03 | 1995-06-20 | Honda Motor Co Ltd | 炭化物粒子分散強化Al合金の製造方法 |
JP2734891B2 (ja) * | 1992-07-02 | 1998-04-02 | トヨタ自動車株式会社 | 金属炭化物粒子分散金属基複合材料の製造方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1289748C (fr) * | 1985-03-01 | 1991-10-01 | Abinash Banerji | Production du carbure de titane |
JPH07300634A (ja) * | 1994-05-02 | 1995-11-14 | Kobe Steel Ltd | AlまたはAl合金複合材料の製法 |
JP4515548B2 (ja) * | 1999-02-15 | 2010-08-04 | 株式会社東芝 | バルク状非晶質合金およびこれを用いた高強度部材 |
-
2000
- 2000-09-25 WO PCT/JP2000/006589 patent/WO2002027055A1/fr active Application Filing
- 2000-09-25 JP JP2002530815A patent/JPWO2002027055A1/ja active Pending
- 2000-09-27 TW TW089119986A patent/TWI235770B/zh not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6475641A (en) * | 1987-09-18 | 1989-03-22 | Takeshi Masumoto | Amorphous alloy containing carbon grain and its manufacture |
JP2734891B2 (ja) * | 1992-07-02 | 1998-04-02 | トヨタ自動車株式会社 | 金属炭化物粒子分散金属基複合材料の製造方法 |
JPH0688154A (ja) * | 1992-09-04 | 1994-03-29 | Mitsubishi Kasei Corp | 金属組成物及び発泡金属組成物の製造方法 |
JPH07157834A (ja) * | 1993-12-03 | 1995-06-20 | Honda Motor Co Ltd | 炭化物粒子分散強化Al合金の製造方法 |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007092103A (ja) * | 2005-09-27 | 2007-04-12 | Japan Science & Technology Agency | 延性を有するマグネシウム基金属ガラス合金−金属粒体複合材 |
JP4602210B2 (ja) * | 2005-09-27 | 2010-12-22 | 独立行政法人科学技術振興機構 | 延性を有するマグネシウム基金属ガラス合金−金属粒体複合材 |
JP2009510267A (ja) * | 2005-10-03 | 2009-03-12 | エーテーハー チューリヒ | バルク金属ガラス/グラファイト複合材料 |
CN102529191A (zh) * | 2011-12-15 | 2012-07-04 | 比亚迪股份有限公司 | 一种非晶合金制品及其制造方法 |
CN105316603A (zh) * | 2015-10-26 | 2016-02-10 | 宋佳 | 一种高韧性非晶合金及其制备方法 |
CN105316604A (zh) * | 2015-10-26 | 2016-02-10 | 宋佳 | 一种高硬度非晶合金及其制备方法 |
CN105316604B (zh) * | 2015-10-26 | 2017-04-19 | 宋佳 | 一种高硬度非晶合金及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
JPWO2002027055A1 (ja) | 2004-02-05 |
TWI235770B (en) | 2005-07-11 |
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