[go: up one dir, main page]

JPH0583623B2 - - Google Patents

Info

Publication number
JPH0583623B2
JPH0583623B2 JP941588A JP941588A JPH0583623B2 JP H0583623 B2 JPH0583623 B2 JP H0583623B2 JP 941588 A JP941588 A JP 941588A JP 941588 A JP941588 A JP 941588A JP H0583623 B2 JPH0583623 B2 JP H0583623B2
Authority
JP
Japan
Prior art keywords
alloy
titanium
melting
melting point
particle size
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 - Lifetime
Application number
JP941588A
Other languages
Japanese (ja)
Other versions
JPH01184239A (en
Inventor
Akihiro Yamanaka
Hiroyuki Ichihashi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Corp
Original Assignee
Sumitomo Metal Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP941588A priority Critical patent/JPH01184239A/en
Publication of JPH01184239A publication Critical patent/JPH01184239A/en
Publication of JPH0583623B2 publication Critical patent/JPH0583623B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention] 【産業上の利用分野】[Industrial application field]

この発明はタンタル、モリブデン、バナジウム
等の高融点で難溶性の元素を含むチタン合金を
VAR(真空アーク溶解炉)、EB(エレクトロンビ
ーム炉)といつた消耗電極式の溶解炉で溶製する
際のチタン合金のコンパクトからなる消耗電極に
関する。
This invention uses titanium alloys containing elements with high melting points and low solubility such as tantalum, molybdenum, and vanadium.
This article relates to consumable electrodes made of compact titanium alloys used in melting in consumable electrode type melting furnaces such as VAR (vacuum arc melting furnace) and EB (electron beam furnace).

【従来の技術】[Conventional technology]

一般にチタン合金のコンパクトからなる消耗電
極は、チヤンバー内で溶解されると同時に、その
下方に配した水冷銅鋳型内に集積し下方から順次
凝固し、最終的にチタン合金鋳塊となる。しか
し、タンタル、モリブデン、タングステンのよう
にチタンより密度がかなり大きく融点の高い元素
は、消耗電極の溶解から銅鋳型での凝固に至る間
で十分に溶融されないまま溶け残りとなつて鋳塊
に残存することがしばしば起る。チタン合金の鋳
塊はプロセス上さらに二次、三次と溶解して偏析
を防止するのが一般的であるが、一次の鋳塊でこ
のような溶け残りを生じると二次、三次の鋳塊に
おいても解消されない場合が多く、ひいては成品
上ハイデンシテイインクルージヨン(高密度介在
物)として問題となる。 このような問題に対処するため、従来より種々
の手法が実施されている。 一般的には添加元素を含む低融点化した母合
金を純成分の代りに配合する方法、スポンジチ
タンと合金添加元素の粉末状のものを混合してコ
ンパクトを作製する方法等がある。の方法とし
ては、例えば80〜400メツシユの添加元素の粉末
体とチタンスポンジを均一に混合して合金溶製用
消耗電極を作製するする方法が知られている(特
公昭46−17413号公報)。
In general, a consumable electrode made of a compact titanium alloy is melted in a chamber, and at the same time, it is accumulated in a water-cooled copper mold placed below it and solidified sequentially from below, eventually becoming a titanium alloy ingot. However, elements such as tantalum, molybdenum, and tungsten, which are much denser than titanium and have higher melting points, remain in the ingot as unmolten material without being sufficiently melted during the process from melting in the consumable electrode to solidification in the copper mold. It often happens. It is common for titanium alloy ingots to be further melted into secondary and tertiary ingots during the process to prevent segregation, but if such unmolten ingots occur in the primary ingot, it will cause problems in the secondary and tertiary ingots. In many cases, these problems are not resolved, and this results in problems as high-density inclusions on the finished product. In order to deal with such problems, various methods have been implemented in the past. In general, there are methods of blending a low-melting-point master alloy containing additive elements in place of the pure components, and a method of preparing a compact by mixing titanium sponge and powdered alloy additive elements. As a method, for example, a method is known in which a consumable electrode for alloy melting is prepared by uniformly mixing 80 to 400 meshes of additive element powder and titanium sponge (Japanese Patent Publication No. 17413/1983). .

【発明が解決しようとする課題】[Problem to be solved by the invention]

しかし、従来の方法には以下に示すような問題
があつた。 従来の方法において、母合金を用いようとする
と、β型合金のように高融点元素を多量に含む場
合、従来のような市販のAl−Mo母合金等の利用
が不可能となる。また、特別にこれらの合金に適
合するように母合金を作製するには多大な工数と
費用を要し、したがつて添加元素の純成分での配
合を行なう方法が有利である。 また、純成分の配合方法としては、前記に示
すように添加元素の金属粉末とスポンジチタンの
混合による方法が有効であると考えられるが、一
般に純金属の粉末体は粒度が小さくなるほど高価
で、しかも酸素等の不純物が混入し易くなる。一
方、添加元素の配合量が多くなれば、低濃度の合
金系では比較的大きな粒径のものでも溶融できた
ものが溶け残りを生じることがしばしば起る。ま
た、80〜400メツシユと一律に添加元素の粒度を
決めた場合、添加元素によつては溶け残りを生じ
ることがある。 この発明は従来の前記課題を解決するためにな
されたもので、チタン合金の消耗電極を構成する
チタンコンパクトへの高融点成分元素を溶け残り
が生じることがないように配合したチタン合金消
耗電極を提案せんとするものである。
However, the conventional method has the following problems. In the conventional method, when attempting to use a master alloy, it becomes impossible to use commercially available Al--Mo master alloys, etc., when the alloy contains a large amount of high melting point elements, such as a β-type alloy. Further, it requires a large amount of man-hours and costs to produce a master alloy specially adapted to these alloys, and therefore it is advantageous to mix the additive elements in pure form. In addition, as a method for blending pure components, it is considered effective to mix the metal powder as an additive element and titanium sponge, as shown above, but in general, the smaller the particle size of pure metal powder, the more expensive it is. Moreover, impurities such as oxygen are likely to be mixed in. On the other hand, when the amount of added elements is increased, even relatively large grain size particles often remain undissolved in a low-concentration alloy system. Furthermore, if the particle size of the additive element is uniformly determined to be 80 to 400 meshes, some undissolved elements may be left undissolved depending on the additive element. This invention was made in order to solve the above-mentioned conventional problems, and provides a titanium alloy consumable electrode in which high melting point constituent elements are blended into the titanium compact constituting the titanium alloy consumable electrode in such a way that no undissolved residue is left. This is what I would like to propose.

【課題を解決するための手段】[Means to solve the problem]

この発明は添加元素の種類、濃度によつてそれ
ぞれ溶け残りなく溶解できる最大の粒径を求め、
これを配合するのが最も効果的であるとの知見に
基づいて、高融点添加元素の純成分の粉末体の最
大粒径を下記(1)式で求まる値以下とすることを特
徴とするものである。
This invention determines the maximum particle size that can be dissolved without any undissolved residue depending on the type and concentration of the added element, and
Based on the knowledge that it is most effective to mix this, the maximum particle size of the powder of the pure component of the high melting point additive element is set to be equal to or less than the value determined by the following formula (1). It is.

【化】 d:添加元素の金属粉末の最大粒径(μm) ρA:添加元素の密度(g/cm3) ρO:チタンの密度(g/cm3) CO A:鋳塊の合金成分の目標濃度(wt%) C※A:チタンと合金成分よりなる二元素系合金
において液相線温度が2000℃となる合金成分
の濃度(wt%) DA:2000℃のチタン溶湯中での合金成分の拡
散係数(cm2/sec) K:溶解炉により定まる係数 なお、(1)式の導出根拠は次のとおりである。 Ti溶湯と添加元素金属粒子の境界層において、 Tiと添加元素の相互拡散量を添加元素の物質
移動として求め、これを添加元素粒子の溶解量に
等しいとし、添加元素金属粉末の粒子径をdAとお
くと(2)式の関係が成り立つ。 ρAd(1/6πd3A)/dt=−α・πd2 A(C※A−C
O A)……(2) ここで、Ti中の添加元素の拡散係数をDAとす
ると理論上、シヤーウツド数Shは(3)式で与えら
れる。 Sh=α・dA/DA=2.0 ……(3) (2),(3)式より粒子径の時間的変化は(4)式で求ま
る。 dA=√A
[Chemical] d: Maximum particle size of metal powder of added element (μm) ρ A : Density of added element (g/cm 3 ) ρ O : Density of titanium (g/cm 3 ) C O A : Ingot alloy Target concentration of component (wt%) C* A : Concentration of alloy component at which the liquidus temperature is 2000℃ in a binary alloy consisting of titanium and alloy component (wt%) D A : In molten titanium at 2000℃ Diffusion coefficient of alloy components (cm 2 /sec) K: coefficient determined by the melting furnace The basis for deriving equation (1) is as follows. In the boundary layer between the Ti molten metal and the additive element metal particles, the mutual diffusion amount of Ti and the additive element is determined as the mass transfer of the additive element, and this is assumed to be equal to the dissolved amount of the additive element particles, and the particle size of the additive element metal powder is d. If we set A , the relationship in equation (2) holds true. ρ A d(1/6πd 3 / A )/dt=-α・πd 2 A (C* A −C
O A )...(2) Here, if the diffusion coefficient of the added element in Ti is D A , the shearwood number Sh is theoretically given by equation (3). Sh=α・d A /D A =2.0 ...(3) From equations (2) and (3), the temporal change in particle diameter can be found using equation (4). dA = √A

Claims (1)

【特許請求の範囲】 1 高融点金属を含有するチタン合金溶製用消耗
電極であつて、高融点添加元素の金属粉末の粒径
を下記(1)式で求まる値以下とすることを特徴とす
る高融点金属を含むチタン合金消耗電極。 【化】 d:添加元素の金属粉末の最大粒径(μm) ρA:添加元素の密度(g/cm3) ρO:チタンの密度(g/cm3) CO A:鋳塊の合金成分の目標濃度(wt%) C※A:チタンと合金成分よりなる二元素系合金
において液相線温度が2000℃となる合金成分
の濃度(wt%) DA:2000℃のチタン溶湯中での合金成分の拡
散係数(cm2/sec) K:溶解炉により定まる係数。
[Claims] 1. A consumable electrode for melting titanium alloy containing a high-melting point metal, characterized in that the particle size of the metal powder of the high-melting point additive element is equal to or less than the value determined by the following formula (1). Titanium alloy consumable electrode containing high melting point metal. [Chemical] d: Maximum particle size of metal powder of added element (μm) ρ A : Density of added element (g/cm 3 ) ρ O : Density of titanium (g/cm 3 ) C O A : Ingot alloy Target concentration of component (wt%) C* A : Concentration of alloy component at which the liquidus temperature is 2000℃ in a binary alloy consisting of titanium and alloy component (wt%) D A : In molten titanium at 2000℃ Diffusion coefficient of alloy components (cm 2 /sec) K: Coefficient determined by the melting furnace.
JP941588A 1988-01-19 1988-01-19 Titanium alloy consumable electrode containing high melting metal Granted JPH01184239A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP941588A JPH01184239A (en) 1988-01-19 1988-01-19 Titanium alloy consumable electrode containing high melting metal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP941588A JPH01184239A (en) 1988-01-19 1988-01-19 Titanium alloy consumable electrode containing high melting metal

Publications (2)

Publication Number Publication Date
JPH01184239A JPH01184239A (en) 1989-07-21
JPH0583623B2 true JPH0583623B2 (en) 1993-11-26

Family

ID=11719754

Family Applications (1)

Application Number Title Priority Date Filing Date
JP941588A Granted JPH01184239A (en) 1988-01-19 1988-01-19 Titanium alloy consumable electrode containing high melting metal

Country Status (1)

Country Link
JP (1) JPH01184239A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0559465A (en) * 1991-08-28 1993-03-09 Nkk Corp Manufacturing method of high activity alloy containing refractory metal element
US7416697B2 (en) 2002-06-14 2008-08-26 General Electric Company Method for preparing a metallic article having an other additive constituent, without any melting
US7897103B2 (en) 2002-12-23 2011-03-01 General Electric Company Method for making and using a rod assembly
JP2005298855A (en) * 2004-04-07 2005-10-27 Toyota Central Res & Dev Lab Inc Titanium alloy and titanium alloy product and method for producing the same
US7531021B2 (en) 2004-11-12 2009-05-12 General Electric Company Article having a dispersion of ultrafine titanium boride particles in a titanium-base matrix
JP2007084888A (en) * 2005-09-22 2007-04-05 Toyota Central Res & Dev Lab Inc Method for producing titanium alloy
CN113462904B (en) * 2021-07-22 2022-12-09 西安汉唐分析检测有限公司 Pressing method of Ti-Mo alloy vacuum consumable electrode bar with high Mo content

Also Published As

Publication number Publication date
JPH01184239A (en) 1989-07-21

Similar Documents

Publication Publication Date Title
JPH0583623B2 (en)
US4088475A (en) Addition of reactive elements in powder wire form to copper base alloys
JP2800137B2 (en) Master alloy for alloy based on beta 21S titanium and method of manufacturing the master alloy
GB2299099A (en) Process for producing grain refining master alloys.
JPH0625774A (en) Production of tib2-dispersed tial-base composite material
US6139654A (en) Strontium master alloy composition having a reduced solidus temperature and method of manufacturing the same
US3508910A (en) Master alloy
US4605436A (en) Method of producing titanium alloys
US4008104A (en) Method for dephosphorization and denitrification of an alloy containing easily oxidizable components
JP2590091B2 (en) Refractory metal silicide target and its manufacturing method
US4014689A (en) Method of fabricating a contact material for high-power vacuum circuit breakers
JPS60228631A (en) Manufacture of titanium alloy
US3997332A (en) Steelmaking by the electroslag process using prereduced iron or pellets
US4014688A (en) Contact material for high-power vacuum circuit breakers
US4582533A (en) Method of and prealloy for the production of titanium alloys
JP2989053B2 (en) Method for producing low oxygen Ti-Al alloy and low oxygen Ti-Al alloy
JPH0995743A (en) Method for producing molten metal-based material, molten metal-based material, and electronic beam melting facility
US3552947A (en) Method for melting titanium base alloys
US3993481A (en) Contact material for high-power vacuum circuit breakers
US3948652A (en) Contact material for high-power vacuum circuit breakers
JP2003293051A (en) Method for producing Ti alloy containing low melting point metal and high melting point metal
US3982925A (en) Method of decarburization in ESR-processing of superalloys
JP3666822B2 (en) Master alloy for adding Zr into Mg alloy
US20030121367A1 (en) Method for eliminating bismuth from molten lead by adding calcium-magnesium alloys
JP2640511B2 (en) Method for producing titanium alloy containing ruthenium and nickel