JPH04333542A - Al-b alloy and its manufacture - Google Patents
Al-b alloy and its manufactureInfo
- Publication number
- JPH04333542A JPH04333542A JP13588891A JP13588891A JPH04333542A JP H04333542 A JPH04333542 A JP H04333542A JP 13588891 A JP13588891 A JP 13588891A JP 13588891 A JP13588891 A JP 13588891A JP H04333542 A JPH04333542 A JP H04333542A
- Authority
- JP
- Japan
- Prior art keywords
- molten metal
- alloy
- alb2
- crystals
- viscosity
- 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 6
- 229910045601 alloy Inorganic materials 0.000 title description 6
- 239000000956 alloy Substances 0.000 title description 6
- 229910052751 metal Inorganic materials 0.000 claims abstract description 27
- 239000002184 metal Substances 0.000 claims abstract description 27
- 229910000521 B alloy Inorganic materials 0.000 claims abstract description 22
- 229910052796 boron Inorganic materials 0.000 claims abstract description 17
- 229910016459 AlB2 Inorganic materials 0.000 claims abstract description 16
- 101000693961 Trachemys scripta 68 kDa serum albumin Proteins 0.000 claims abstract description 16
- 239000013078 crystal Substances 0.000 claims abstract description 16
- 229910020491 K2TiF6 Inorganic materials 0.000 claims abstract description 15
- 229910020261 KBF4 Inorganic materials 0.000 claims abstract description 11
- 230000004907 flux Effects 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 claims abstract description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 15
- 238000000926 separation method Methods 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 abstract description 12
- 238000005266 casting Methods 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 229910052782 aluminium Inorganic materials 0.000 description 10
- 239000000463 material Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910000765 intermetallic Inorganic materials 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 230000016507 interphase Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明はアルミニウム電線の導電
性改良材および中性子吸収材として使用されるAl−B
合金およびその製造方法に関する。[Industrial Application Field] The present invention relates to Al-B used as a conductivity improver and neutron absorber for aluminum electric wires.
Related to alloys and their manufacturing methods.
【0002】0002
【従来の技術】U.S.P.3503738に開示され
ている如く、AlメタルをKBF4と共にブリケットに
し、アルミニウム溶湯に添加し、900℃で反応させ、
反応温度を1000℃以上にしてAl−B合金を製造し
ている。また特開昭62−1834には、660〜80
0℃のAl溶湯にホウフッ化物を添加してAl−B2金
属間化合物を製造する際に、フッ化アルカリを添加し、
反応温度を制御す方法が開示されている。Al−B製造
方法に於いて、反応温度を900℃以上に上げると、A
lB2が全てAlB12結晶に変化してしまい、AlB
12ではアルミニウムの導電性の改良の効果が低下する
欠点を生ずる。また溶湯温度を660〜800℃で行う
方法では、AlB2が生成するが、Al−B溶湯の粘性
が大きくなり、フッ化アルカリの添加だけではフラック
スの分離が難しく、フラックスが製品の中に多量混入す
る欠点を有すると共に、溶湯の粘性が悪く、鋳型に鋳込
めない欠点を有していた。[Prior Art] U. S. P. 3503738, Al metal is briquetteted with KBF4, added to molten aluminum, reacted at 900°C,
The Al-B alloy is manufactured at a reaction temperature of 1000°C or higher. Also, in JP-A-62-1834, 660-80
When adding borofluoride to 0°C Al molten metal to produce an Al-B2 intermetallic compound, alkali fluoride is added,
A method of controlling reaction temperature is disclosed. In the Al-B manufacturing method, when the reaction temperature is raised to 900°C or higher, A
All lB2 changes to AlB12 crystals, and AlB
No. 12 has the disadvantage that the effect of improving the conductivity of aluminum is reduced. In addition, in the method in which the molten metal temperature is 660 to 800°C, AlB2 is generated, but the viscosity of the Al-B molten metal increases, and it is difficult to separate the flux just by adding alkali fluoride, resulting in a large amount of flux mixed into the product. In addition, the molten metal had poor viscosity and could not be cast into a mold.
【0003】0003
【発明が解決しようとする課題】本発明が解決しようと
する課題は、従来のAl−B合金就中アルミニウム電線
製造用原料であるAl−B合金の上記難点を解消するこ
とである。OBJECTS OF THE INVENTION The problem to be solved by the present invention is to solve the above-mentioned disadvantages of conventional Al-B alloys, especially Al-B alloys which are raw materials for producing aluminum electric wires.
【0004】0004
【課題を解決するための手段】発明者らはクラスターの
少ないAlB2結晶のみから成るAl−B合金の製法を
種々検討した結果、反応温度を680〜850℃の範囲
でKBF4をアルミニウムと反応させ、生成したAlB
2結晶を含むAl−B合金溶湯にK2TiF6を少量添
加することにより、粘性の低い鋳込易いAl−B合金が
収得出来ることを見い出した。[Means for Solving the Problems] The inventors investigated various methods for producing an Al-B alloy consisting only of AlB2 crystals with few clusters, and found that KBF4 is reacted with aluminum at a reaction temperature in the range of 680 to 850°C. Generated AlB
It has been found that by adding a small amount of K2TiF6 to a molten Al-B alloy containing two crystals, an Al-B alloy with low viscosity and easy to cast can be obtained.
【0005】[0005]
【発明の構成並びにその作用】AlB2は920℃でA
lB12に転移する〔阿東田、東、小林、Sci.Pa
t.Inst.Phys.Chem.Rev.61(3
),92(1967)〕ので、AlとKBF4との反応
の発熱を制御し、反応時の温度上昇を押さえることが大
切である。AlB12への転移は920℃であるが、A
l−B相間化合物の結晶形をAlB2に保持し、しかも
溶湯の粘性を良い状態に保つには温度が850℃を超え
ないようにしなければならない。Structure of the invention and its operation: AlB2 has A at 920°C.
metastasizes to lB12 [Atoda, Higashi, Kobayashi, Sci. Pa
t. Inst. Phys. Chem. Rev. 61(3
), 92 (1967)], it is important to control the heat generation of the reaction between Al and KBF4 and suppress the temperature rise during the reaction. The transition to AlB12 is at 920°C, but A
In order to maintain the crystalline form of the l-B interphase compound in AlB2 and to maintain the viscosity of the molten metal in a good state, the temperature must not exceed 850°C.
【0006】Al溶湯を730℃に保ちKBF4を添加
していくと、発熱反応で800℃位に達するので、添加
を中止し、再び730℃迄温度を低下させ、再びKBF
4を添加する。このようにして温度を850℃以下好ま
しくは780℃以下に制御しながらKBF4をAlと反
応させる。このとき生成したAl−B溶湯は非常に粘性
が高い。特にB含量が5重量%以上では溶湯の撹拌が困
難となる。この溶湯を採取し、冷却固化させ、合金の組
織検査をすると、AlB2結晶が、網目模様に結合して
いることが明らかとなった。この網目構造が粘性の増大
の原因であることが判明した。この網目を破壊する方法
を種々検討した結果、K2TiF6処理すると、この網
目構造が破壊され、Al−B溶湯の粘性が下がることを
見い出した。元来アルミニウムメタルにTiは0.01
%以下含まれているが、このTiはKBF4添加時にT
iB2に変化してしまい、Al−B合金生成時の網目構
造切断には効果を示さない。網目構造形成後に添加する
K2TiF6中のTiが還元され溶湯に溶け込み、網目
のAlBを切断するのである。この粘性の悪い撹拌困難
なAl−B溶湯にK2TiF6を最適量添加すると、た
だちに溶湯の粘性がよくなり(低下し)、楽に撹拌でき
るようになった。またルツボからの流出も容易で、任意
の鋳型に流し込むことが出来た。K2TiF6処理した
Al−B溶湯を採取し、冷却固化させ、合金の組織検査
をすると、AlB2結晶が独立に存在し、網目模様は完
全に消失していた。このようにK2TiF6処理したA
l−B合金はTiを0.001〜0.05%含有し、し
かもホウ素は全てAlB2結晶となり、Al中に独立し
て存在していた。Al合金中のTiは導電性を悪くする
と云われているが、ここに含有されているTiはTiB
2になっており、アルミニウムの導電性を低下させない
ことが認められた。発明に於いてはホウ素含有量7%迄
製造可能である。When KBF4 is added while keeping the Al molten metal at 730°C, the temperature reaches about 800°C due to an exothermic reaction, so the addition is stopped, the temperature is lowered to 730°C again, and KBF4 is added again.
Add 4. In this way, KBF4 is reacted with Al while controlling the temperature to 850°C or lower, preferably 780°C or lower. The Al-B molten metal produced at this time has a very high viscosity. In particular, if the B content is 5% by weight or more, it becomes difficult to stir the molten metal. When this molten metal was sampled, cooled and solidified, and the structure of the alloy was examined, it was revealed that AlB2 crystals were bonded in a network pattern. This network structure was found to be the cause of the increase in viscosity. As a result of examining various methods for destroying this network, it was found that K2TiF6 treatment destroys this network structure and lowers the viscosity of the Al-B molten metal. Originally, Ti was 0.01 in aluminum metal.
% or less, but when KBF4 is added, this Ti
It changes to iB2 and has no effect on cutting the network structure during Al-B alloy formation. Ti in K2TiF6 added after the network structure is formed is reduced and dissolved into the molten metal, cutting the AlB network. When an optimal amount of K2TiF6 was added to this Al-B molten metal, which had poor viscosity and was difficult to stir, the viscosity of the molten metal immediately improved (reduced) and it became possible to stir it easily. It was also easy to drain from the crucible and could be poured into any mold. When the K2TiF6-treated Al-B molten metal was collected, cooled and solidified, and the structure of the alloy was examined, it was found that AlB2 crystals existed independently and the network pattern had completely disappeared. A treated with K2TiF6 in this way
The 1-B alloy contained 0.001 to 0.05% Ti, and all boron was formed into AlB2 crystals and existed independently in Al. It is said that Ti in Al alloys deteriorates conductivity, but the Ti contained here is
2, and it was recognized that the conductivity of aluminum was not reduced. In the present invention, it is possible to produce a material with a boron content of up to 7%.
【0007】KBF4とAlとの反応で生成する粘性の
悪いAl−B合金溶湯をK2TiF6処理によるAl−
B合金溶湯の粘性改善により、ホウ素含有量が多くなっ
てもクラスターの少ないAlB2結晶だけを含有する高
ホウ素濃度のAl−B合金が容易に製造可能となった。
その結果、アルミニウムの導電性改善の効率が向上し、
又中性子吸収用アルミニウム材の製造が容易となった。[0007] The molten Al-B alloy with poor viscosity produced by the reaction between KBF4 and Al is treated with Al-B by K2TiF6 treatment.
By improving the viscosity of the molten B alloy, it has become possible to easily produce an Al-B alloy with a high boron concentration that contains only AlB2 crystals with few clusters even when the boron content is increased. As a result, the efficiency of improving the conductivity of aluminum increases,
Also, it has become easier to manufacture aluminum materials for neutron absorption.
【0008】[0008]
【実施例】本発明の技術内容を明確にするために、代表
的な例を抽出して実施例として例示する。
実施例1.黒鉛ルツボに360kgのアルミニウムを入
れ溶解し740℃に保つ。これにまずKBF485kg
を投入して反応させる。反応温度は820℃まで上昇し
た。上層の生成フラックスを除去した後、KBF488
kgを添加する。この工程以降の反応温度は最高780
℃までで行った。続いて少量のK2TiF6を添加し、
Al−B溶湯の粘性を調整する。残りのKBF415k
gを投入し、反応させた後、更にK2TiF6添加し、
溶湯の粘性を調整する。調整終了後フラックスを除去し
、Al−B合金溶湯を鋳型に鋳込む。Al−4%B合金
340kgが得られた。このもののTi含有量は0.0
1%およびホウ素含有量は4.2%であった。合金の組
織検査の結果、ホウ素の結晶は全てAlB2であると共
にAl中に独立して存在していた。またクラスターもほ
とんど認められなかった。
実施例2.溶解アルミニウム360kgを黒鉛ルツボに
入れ、温度を720℃にする。これにKBF4100K
gを添加する。反応温度は上昇するが最高820℃に制
御する。生成フラックスを除去した後、KBF4100
kgを反応添加させた。この時点でメタル溶湯の粘度が
かなり増し、フラックスとメタルの分離状況が悪くなっ
た。K2TiF6を少量添加し、Al−B溶湯の粘性を
改善し撹拌効率を上げる生成フラックスを再度除去した
後、KBF488kgを添加した。再度K2TiF6を
添加し、Al−B溶湯の粘性を低下させ、流動性をよく
する。生成フラックスを除去後、鋳型に鋳込んでAl−
5%B合金305kgを得た。この合金の組織検査をし
た結果、結晶はAlB2であり、網目構造は認められな
かった。またクラスターの存在もほとんど認められなか
った。このもののTi含有量は0.02%であり、硼素
の含有量は5.3%であった。
実施例3.Al溶湯304kgを720℃に保ち、これ
にKBF4250kgを3回に分割し実施例2と同じ操
作を行った。その結果粘性の良いホウ素6.3%含有の
Al−6%B合金250kgを得た。このもののTi含
有量は0.04%であり、ホウ素の金属間化合物は全て
AlB2結晶であった。
実施例4.720℃に保ったAl溶湯365KgKBF
4150Kgを2回に分割して投入した。投入終了後、
K2TiF6を添加し、Al−B溶湯の粘性を改善した
。生成フラックスを除去後、鋳型に流し込みホウ素3.
10%含むAl−3%B合金340kgを得た。このも
ののTi含有量は0.01%であり、ホウ素は全てAl
B2結晶から成っていた。EXAMPLES In order to clarify the technical content of the present invention, representative examples will be extracted and illustrated as examples. Example 1. 360 kg of aluminum is placed in a graphite crucible, melted, and kept at 740°C. First of all, KBF485kg
Inject and react. The reaction temperature rose to 820°C. After removing the upper layer generated flux, KBF488
Add kg. The reaction temperature after this step is up to 780℃.
It was carried out at temperatures up to ℃. Then add a small amount of K2TiF6,
Adjust the viscosity of Al-B molten metal. remaining KBF415k
After adding and reacting, K2TiF6 was added,
Adjust the viscosity of molten metal. After the adjustment is completed, the flux is removed and the molten Al-B alloy is poured into a mold. 340 kg of Al-4%B alloy was obtained. The Ti content of this is 0.0
1% and the boron content was 4.2%. As a result of microstructural examination of the alloy, all boron crystals were AlB2 and independently present in Al. In addition, almost no clusters were observed. Example 2. 360 kg of molten aluminum is placed in a graphite crucible and the temperature is brought to 720°C. KBF4100K for this
Add g. Although the reaction temperature increases, it is controlled at a maximum of 820°C. After removing the generated flux, KBF4100
kg was reacted. At this point, the viscosity of the molten metal increased considerably, and the separation of the flux and metal deteriorated. After adding a small amount of K2TiF6 and again removing the generated flux that improves the viscosity of the Al-B melt and increases the stirring efficiency, 488 kg of KBF was added. K2TiF6 is added again to reduce the viscosity of the Al-B molten metal and improve its fluidity. After removing the generated flux, it is poured into a mold and Al-
305 kg of 5% B alloy was obtained. As a result of microstructural examination of this alloy, it was found that the crystals were AlB2 and no network structure was observed. Furthermore, the presence of clusters was hardly recognized. The Ti content of this material was 0.02%, and the boron content was 5.3%. Example 3. The same operation as in Example 2 was carried out by keeping 304 kg of molten Al at 720° C. and dividing 4250 kg of KBF into this into three portions. As a result, 250 kg of Al-6% B alloy containing 6.3% boron and having good viscosity was obtained. The Ti content of this material was 0.04%, and all boron intermetallic compounds were AlB2 crystals. Example 4. 365Kg KBF of Al molten metal kept at 720℃
4,150 kg was divided into two doses. After the input is complete,
K2TiF6 was added to improve the viscosity of the Al-B molten metal. After removing the generated flux, pour it into a mold and add boron 3.
340 kg of Al-3% B alloy containing 10% was obtained. The Ti content of this material is 0.01%, and all boron is Al.
It consisted of B2 crystals.
Claims (2)
ホウ素を2〜7重量%含有し、ホウ素が全てAlB2結
晶からなることを特徴としたAl−B合金。1. An Al-B alloy containing 0.001 to 0.05% by weight of Ti and 2 to 7% by weight of boron, and characterized in that all of the boron consists of AlB2 crystals.
てAlB2結晶とした後、K2TiF6を添加しAl−
B溶湯の粘性を調整し、フラックスの分離をよくすると
共に鋳込み易いAl−B合金の製造を680−850℃
の温度域で行うことを特徴とするホウ素含有2〜7%の
Al−B合金の製造方法。Claim 2: Add KBF4 to molten Al to convert all boron into AlB2 crystals, and then add K2TiF6 to form Al-
Adjusting the viscosity of the B molten metal, improving flux separation, and producing an easy-to-cast Al-B alloy at 680-850℃
A method for producing an Al-B alloy containing 2 to 7% boron, characterized in that the process is carried out in a temperature range of 2 to 7%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3135888A JP2535678B2 (en) | 1991-05-09 | 1991-05-09 | Method for producing Al-B alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3135888A JP2535678B2 (en) | 1991-05-09 | 1991-05-09 | Method for producing Al-B alloy |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04333542A true JPH04333542A (en) | 1992-11-20 |
JP2535678B2 JP2535678B2 (en) | 1996-09-18 |
Family
ID=15162142
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3135888A Expired - Lifetime JP2535678B2 (en) | 1991-05-09 | 1991-05-09 | Method for producing Al-B alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2535678B2 (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2733997A1 (en) * | 1995-05-01 | 1996-11-15 | Kobe Steel Ltd | Aluminium@ alloys containing boron isotopes |
GB2361934A (en) * | 2000-03-03 | 2001-11-07 | Kobe Steel Ltd | Boron containing aluminium alloy |
WO2003012155A1 (en) * | 2001-07-30 | 2003-02-13 | Jfe Engineering Corporation | Material being resistant to chloride-containing molten salt corrosion, steel pipe for heat exchanger coated with the same, and method for production thereof |
JP2007533851A (en) * | 2004-04-22 | 2007-11-22 | アルキャン・インターナショナル・リミテッド | Improved neutron absorption efficiency of boron-containing aluminum materials |
CN103374666A (en) * | 2012-04-19 | 2013-10-30 | 包头铝业有限公司 | Preparation method of aluminum boron intermediate alloy |
CN105671343A (en) * | 2016-03-25 | 2016-06-15 | 沈阳大学 | Preparation method of aluminum boron intermediate alloy wire for electrician aluminum melt purification |
CN108796261A (en) * | 2018-06-06 | 2018-11-13 | 湘潭大学 | A kind of in-situ self-generated TiB2Particle enhanced aluminum-based composite material and preparation method thereof |
CN109161708A (en) * | 2018-11-13 | 2019-01-08 | 河北四通新型金属材料股份有限公司 | A kind of high-purity high concentration of aluminium boron intermediate alloy and preparation method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61235523A (en) * | 1985-04-11 | 1986-10-20 | Kobe Steel Ltd | Manufacture of al-b alloy |
JPS62235437A (en) * | 1986-04-04 | 1987-10-15 | Showa Alum Corp | Production of aluminum alloy extruded material having excellent neutron absorptivity |
-
1991
- 1991-05-09 JP JP3135888A patent/JP2535678B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61235523A (en) * | 1985-04-11 | 1986-10-20 | Kobe Steel Ltd | Manufacture of al-b alloy |
JPS62235437A (en) * | 1986-04-04 | 1987-10-15 | Showa Alum Corp | Production of aluminum alloy extruded material having excellent neutron absorptivity |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2733997A1 (en) * | 1995-05-01 | 1996-11-15 | Kobe Steel Ltd | Aluminium@ alloys containing boron isotopes |
GB2361934A (en) * | 2000-03-03 | 2001-11-07 | Kobe Steel Ltd | Boron containing aluminium alloy |
GB2361934B (en) * | 2000-03-03 | 2003-05-14 | Kobe Steel Ltd | Aluminum base alloy containing boron and manufacturing method thereof |
US7125515B2 (en) | 2000-03-03 | 2006-10-24 | Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) | Aluminum base alloy containing boron and manufacturing method thereof |
WO2003012155A1 (en) * | 2001-07-30 | 2003-02-13 | Jfe Engineering Corporation | Material being resistant to chloride-containing molten salt corrosion, steel pipe for heat exchanger coated with the same, and method for production thereof |
JP2007533851A (en) * | 2004-04-22 | 2007-11-22 | アルキャン・インターナショナル・リミテッド | Improved neutron absorption efficiency of boron-containing aluminum materials |
CN103374666A (en) * | 2012-04-19 | 2013-10-30 | 包头铝业有限公司 | Preparation method of aluminum boron intermediate alloy |
CN105671343A (en) * | 2016-03-25 | 2016-06-15 | 沈阳大学 | Preparation method of aluminum boron intermediate alloy wire for electrician aluminum melt purification |
CN108796261A (en) * | 2018-06-06 | 2018-11-13 | 湘潭大学 | A kind of in-situ self-generated TiB2Particle enhanced aluminum-based composite material and preparation method thereof |
CN109161708A (en) * | 2018-11-13 | 2019-01-08 | 河北四通新型金属材料股份有限公司 | A kind of high-purity high concentration of aluminium boron intermediate alloy and preparation method thereof |
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