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JPS6050144A - Alloy cast iron - Google Patents

Alloy cast iron

Info

Publication number
JPS6050144A
JPS6050144A JP15582783A JP15582783A JPS6050144A JP S6050144 A JPS6050144 A JP S6050144A JP 15582783 A JP15582783 A JP 15582783A JP 15582783 A JP15582783 A JP 15582783A JP S6050144 A JPS6050144 A JP S6050144A
Authority
JP
Japan
Prior art keywords
cast iron
molten
parts
aluminum
alloy
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
Application number
JP15582783A
Other languages
Japanese (ja)
Other versions
JPH0565575B2 (en
Inventor
Kihachirou Nishiuchi
西内 紀八郎
Kenichi Wada
和田 憲一
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.)
Otsuka Chemical Co Ltd
Otsuka Kagaku Yakuhin KK
Original Assignee
Otsuka Chemical Co Ltd
Otsuka Kagaku Yakuhin KK
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 Otsuka Chemical Co Ltd, Otsuka Kagaku Yakuhin KK filed Critical Otsuka Chemical Co Ltd
Priority to JP15582783A priority Critical patent/JPS6050144A/en
Publication of JPS6050144A publication Critical patent/JPS6050144A/en
Publication of JPH0565575B2 publication Critical patent/JPH0565575B2/ja
Granted legal-status Critical Current

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  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To provide a alloy cast iron having the higher resistance to corrosion with a molten Al alloy than the conventional FC cast iron and other cast iron by adding the alkali metal salt of titanic acid and boron compd. and further Al to the molten cast iron. CONSTITUTION:The alkali metal salt of titanic acid (e.g.; lithium titaniate) and boron compd. (e.g.; borax) and further Al are added to the molten cast iron used thus far and the molten metal discharge from a melting device is cast to cast a cast iron alloy. The melting temp. in this stage is 1,550-1,800 deg.C, the tapping temp. is 1,500-1,650 deg.C and the casting temp. is 1,450-1,600 deg.C, which are higher than in ordinary conditions. The amt. of the alkali metal salt of titanic acid to be used in this stage is 1.5-10%, more particularly about 2.0-7.0% with respect to the FC component. The amt. of boron compd. to be added is about 0.5-3kg to 120kg molten cast iron. The content of C in the alloy cast iron is 2.5-4.0wt%, more particularly 3.0-3.8wt.%.

Description

【発明の詳細な説明】 本発明は新しい複合合金鋳鉄に関し、更に詳しくは鋳鉄
溶湯に、チタン酸アルカリ金属塩とホウ素化合物または
更にこれにアルミニウムを添加して成る複合合金鋳鉄に
係る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a new composite alloy cast iron, and more particularly to a composite alloy cast iron made by adding an alkali metal titanate and a boron compound or further aluminum to molten cast iron.

本発明の合金鋳鉄は耐熱及び耐食性を有する特殊合金鋳
鉄の材質研究の過程で見い出されたもので特にアルミニ
ウム溶湯に対し耐久性の高い性能を有する合金鋳鉄であ
る。
The alloy cast iron of the present invention was discovered in the process of material research for special alloy cast iron that has heat resistance and corrosion resistance, and is an alloy cast iron that has particularly high durability against molten aluminum.

従来、アルミニウム台金、亜鉛合金、マグネシウム合金
、錫合金などの非鉄軽金属合金の低圧鋳造用器材やダイ
キャスト用器拐、例えばストーク、るつぼ、熱雷対保護
管、自動給温用ラドルなどにはFC20〜25の普通鋳
鉄が使用されている。
Conventionally, equipment for low-pressure casting and die-casting of nonferrous light metal alloys such as aluminum base metals, zinc alloys, magnesium alloys, and tin alloys, such as stalks, crucibles, thermal lightning protection tubes, and automatic heating ladles, etc. Ordinary cast iron with FC20-25 is used.

しかしながらこれら普通鋳鉄は例えばアルミニウム溶湯
などに対する溶損が大きく、長期の使用に耐えないうえ
に、鉄成分や炭素成分の混入によってアルミニウム鋳造
品等の品質低下をもたらしている。
However, these ordinary cast irons suffer from a large amount of corrosion loss against, for example, molten aluminum, and cannot withstand long-term use. In addition, the quality of aluminum castings is degraded due to the contamination of iron and carbon components.

本発明者は、上記の事実に鑑み、これら普通鋳鉄に替わ
る新規な材料をめる一連の研究の中で、ダクタイル鋳鉄
、ミーバーナイト鋳鉄、高アルミニウム鋳鉄(クラルフ
ァー鋳鉄、アルシロン鋳鉄)など従来公知の特殊鋳鉄よ
りアルミニウム低圧鋳造用のストークを作成し、実操業
を行なって検討して来たが、FC鋳鉄からなる器材の3
〜6日の耐用日数に対して、2〜3倍程度の耐用日数の
上昇程度にとどまった。
In view of the above facts, the present inventor has carried out a series of research into new materials to replace these ordinary cast irons, and has conducted research on conventionally known materials such as ductile cast iron, Mieburnite cast iron, and high aluminum cast iron (Kralfer cast iron, Alsilon cast iron). We have created a stalk for aluminum low-pressure casting from special cast iron, and conducted actual operations to investigate the problem.
Compared to the lifespan of ~6 days, the lifespan only increased by about 2 to 3 times.

そこであくまでも鋳鉄を基本にして、鋳鉄複合合金鋳鉄
の体質を改善すべ〈従来の鋳造工学の常識にとられれる
ことなく新たな発想を展開させることによって本発明の
完成に至ったのである。即ち鋳鉄溶湯中にチタン酸アル
カリ金B塩を添加づることによって今までのFC鋳鉄や
その他の鋳鉄よりもはるかにアルミニウム台金溶湯に対
して耐食性のある材質が安定して得られ、しかも鋳鉄中
の最適配合比率と鋳鉄製造時の温度条件のR適範囲を設
定することによって、またチタン酸アルカリ金属を添加
した鋳鉄溶湯に更にアルミニウムを添加して1%られる
複合合金鋳鉄が上述のように鋳鉄中の最適配合比率、ア
ルミニウム添加比率、複合合金鋳鉄製造時の最適温度範
囲を条件づけることによりチタン酸アルカリ金属を鋳鉄
溶湯に添加するだけでも効果がある上にさらに良好な材
料が得られることが判明した。
Therefore, based on cast iron, it was necessary to improve the constitution of cast iron composite alloy cast iron.The present invention was completed by developing a new idea without being bound by the common sense of conventional casting engineering. In other words, by adding alkali gold titanate B salt to molten cast iron, it is possible to stably obtain a material that is much more resistant to corrosion against molten aluminum base metal than conventional FC cast iron or other cast irons. By setting the optimum blending ratio of and the appropriate range of R for the temperature conditions during cast iron manufacturing, composite alloy cast iron made by adding 1% aluminum to the molten cast iron containing alkali metal titanates can be made into cast iron as described above. By adjusting the optimal blending ratio, aluminum addition ratio, and optimal temperature range during composite alloy cast iron production, we have found that simply adding alkali metal titanate to molten cast iron can be effective and produce even better materials. found.

本発明者は上記新しい木実に基づき更に研究を続けた結
果、鋳鉄溶湯に上記チタン酸アルカリ金属又はこれとア
ルミニウムとを添加量る際に、更にホウ素化合物を共存
せしめる時は、得られる目的物たる合金鋳鉄の組織がよ
り緻密化し、この結果更に耐食性及び耐熱性が向上する
ことを見出し、ここに本発明を完成したものである。
As a result of further research based on the above-mentioned new fruit, the inventor of the present invention found that when adding the above-mentioned alkali metal titanate or aluminum together with the above-mentioned alkali metal titanate to molten cast iron, when a boron compound is further coexisted, the desired product can be obtained. It was discovered that the structure of alloyed cast iron becomes more dense, and as a result, corrosion resistance and heat resistance are further improved, and the present invention has now been completed.

本発明合金鋳鉄をその製造方法に基づいて下記に説明す
る。
The alloy cast iron of the present invention will be explained below based on its manufacturing method.

本発明に於いては鋳鉄溶湯にチタン酸アルカリ金属塩及
びホウ素化合物、或いは更にアルミニウムを添加する。
In the present invention, an alkali metal titanate and a boron compound, or further aluminum are added to the molten cast iron.

この際の鋳鉄溶湯としては従来から使用されて来たもの
が使用出来、たとえば新銑必要に応じ一部故銑を使用し
、これに鋼材、]−クス、石灰石、珪素源を溶解して得
られる鋳鉄溶湯である。これ等各成分は得られる目的物
たる合金鋳鉄の組成を考慮して適宜に配合さける。好ま
しい配合は、得られる合金鋳鉄がC:2.5〜4.0重
量%く以下単に%という)、Si:2.0 〜4 、 
0 % 、Ti:0.05 〜1 % 、ま lこはC
:2.5〜4.0、Si:2.2〜3.8%、Cr二〇
、2〜2%、Mn:0.1〜2%、Ti :0.05〜
1%。Ai2:1.5〜4.0%になる様な配合である
。珪素源としてはフェロシリコン、フェロクロム、フェ
ロマンガン等が好ましいものとして挙げられる。
The molten cast iron used in this case can be the one that has been conventionally used, such as fresh pig iron or partially used iron if necessary, and melting steel, ash, limestone, and a silicon source into the molten metal. It is molten cast iron. These components are appropriately mixed in consideration of the composition of the target alloyed cast iron to be obtained. A preferred composition is that the resulting cast iron alloy contains C: 2.5 to 4.0% by weight (hereinafter simply referred to as %), Si: 2.0 to 4%,
0%, Ti: 0.05 to 1%, C
:2.5~4.0, Si:2.2~3.8%, Cr20,2~2%, Mn:0.1~2%, Ti:0.05~
1%. The composition is such that Ai2: 1.5 to 4.0%. Preferred silicon sources include ferrosilicon, ferrochrome, and ferromanganese.

本発明に於いては上記鋳鉄溶湯にチタン酸アルカリ金属
及びホウ元素化合物を添加し、或いはアルミニウムを更
に添加し、溶解装置から出て来た溶湯を鋳込んで合金を
製造する。この際の溶解温度は1550〜1800℃、
出湯温度は1500〜1650℃、鋳込み湿度1450
〜1600℃好ましくは150Q〜1600℃程度であ
り、通常の条件よりも高温である。
In the present invention, an alkali metal titanate and a boron element compound are added to the molten cast iron, or aluminum is further added, and the molten metal coming out of the melting device is poured to produce an alloy. The melting temperature at this time is 1550-1800℃,
Tapping temperature is 1500-1650℃, casting humidity 1450℃
~1600°C, preferably about 150Q~1600°C, which is higher than normal conditions.

この際使用されるチタン酸アルカリ金属としては、粉状
でもまたlll状状ものでも良く、たとえばチタン酸リ
チウム、チタン酸ナトリウム、チタン酸カリウムを好ま
しいものとして例示出来、ルビジウムやセシウムの塩等
は実用的に特に好ましいものとは云い難い。チタン酸ア
ルカリ金属塩の添加量はFC分に対し1.5〜10%好
ましくは2.0〜7.0%程度である。またホウ素化合
物としてはホウ酸ナトリウム(ホウ砂)、ホウ酸力り、
無水ホウ酸、フェロホウ素等を好ましいものとして例示
出来、これ等の添加量は鋼材120k(1に対し、0.
5〜3kg程度である。
The alkali metal titanate used in this case may be in the form of powder or lll, and examples of preferable examples include lithium titanate, sodium titanate, and potassium titanate, and salts of rubidium and cesium are suitable for practical use. It is hard to say that it is particularly preferable. The amount of the alkali metal titanate added is about 1.5 to 10%, preferably about 2.0 to 7.0%, based on the FC content. In addition, boron compounds include sodium borate (borax), boric acid strength,
Preferred examples include boric anhydride, ferroboron, etc., and the amount of these added is 0.0 to 120k of steel material (1.
It is about 5 to 3 kg.

本発明の鋳鉄並びに複合合金鋳鉄製造装置は古くから用
いられているキューボラ類ばかりでなく電気溶解炉でも
可能であり、キューボラ類の場合、チタン酸アルカリ金
属の飛散をなくするために塊状にして用いることが好ま
しい。
The apparatus for producing cast iron and composite alloy cast iron of the present invention can be used not only for cubelas, which have been used for a long time, but also for electric melting furnaces, and in the case of cubelas, they are used in the form of lumps to prevent the scattering of alkali metal titanates. It is preferable.

本発明に用いられる複合合金鋳鉄中の元素であるCは2
.5〜4〜O重倒%好ましくは3.0〜3.8%のカー
ボン比率である。カーボンが4.0%よりも多くなると
、投合合金鋳鉄は硬くなり過ぎ切削等の後加工が困難に
なるどどもに、もろくなる為に例えばアルミニウム溶湯
などに使用する際の熱ショックに際しクラックの入る恐
れがある。また、2.5%より下になると、合金鋳鉄組
織はフェライト(純鉄)地が多くなり、フェライトはア
ルミニウムと反応してアルミフェライトとなり易い性質
を有する為に、アルミニウム溶湯中に溶出する結果とな
り腐食し易くなる。またSiは2.0〜4.0重口%好
ましくは2.2〜3.8mfi%である。Siが4.0
%よりも多くなると、3iの有する黒鉛化促進元素の性
質により、合金鋳鉄の組織が黒鉛とフエライ1〜地の組
織となり、フェライト地が上記の様に痕食し易くなる。
The element C in the composite alloy cast iron used in the present invention is 2
.. The carbon ratio is preferably 3.0 to 3.8%. If the carbon content exceeds 4.0%, the alloyed cast iron becomes too hard, making post-processing such as cutting difficult, and becomes brittle, causing cracks to form during thermal shock when used in molten aluminum, for example. There is a fear. Furthermore, below 2.5%, the alloy cast iron structure becomes dominated by ferrite (pure iron), and ferrite tends to react with aluminum to form aluminum ferrite, resulting in it being leached into the molten aluminum. It becomes easy to corrode. Further, the content of Si is 2.0 to 4.0 mfi%, preferably 2.2 to 3.8 mfi%. Si is 4.0
%, the structure of the alloyed cast iron becomes a structure of graphite and ferrite 1 to 1 to 100% due to the properties of the graphitization-promoting element contained in 3i, and the ferrite becomes susceptible to corrosion as described above.

更には偏析によりSlが単独で存在し易くなり、アルミ
ニウム溶湯中へ溶出した場合、一般にかにがわくと称さ
れる発泡の原因ともなる。
Furthermore, due to segregation, Sl tends to exist alone, and if it is eluted into the molten aluminum, it may cause foaming, which is generally referred to as foaming.

また、2%よりも下になると耐熱性が悪くなり例えばア
ルミニウム溶湯中で使用される場合の耐熱性が問題どな
る。
Moreover, if it is less than 2%, the heat resistance deteriorates, and for example, the heat resistance becomes a problem when used in molten aluminum.

チタン酸アルカリ金属塩より添加されるT1はキューボ
ラ操業においては0.05〜1重ω%の範囲内となる。
T1 added from the alkali metal titanate is in the range of 0.05 to 1% by weight in Cubola operation.

一般に酸素ガス、或いはハロゲンガス等の腐食性ガスは
合金鋳鉄に侵入する揚台黒鉛を通路として入ることが知
られている。従って、長mra、及び(或いは)それら
m維が連なった黒鉛は、腐食性ガスを容易に侵入させ得
る為に、腐食、或いはクラックの原因となる。そこで、
黒鉛繊維は片状微細化する必要があるが、Tiは黒鉛の
微細化剤として非常に有効であり、従って耐食性のよい
合金鋳鉄が得られる。
It is generally known that corrosive gases such as oxygen gas or halogen gas enter the alloy cast iron through the platform graphite. Therefore, long mra and/or graphite in which these m fibers are connected can easily allow corrosive gases to enter, causing corrosion or cracks. Therefore,
Graphite fibers need to be refined into flakes, and Ti is very effective as a graphite refining agent, so that alloyed cast iron with good corrosion resistance can be obtained.

その他、黒鉛安定化が元素としてC「が0.2〜2重燈
%及び(或いは)Mnが0.1〜2重量%存在する方が
より耐食性を向上し、また合金鋳鉄の耐熱性向上の為に
ΔQが1.5〜4.0%存在する方が望ましい。また、
アルミニウムに関しても、4.0%よりも多く添加する
とΔQの偏析或いは、合金鋳鉄rB湯の海流れが悪くな
り、例えばストークを鋳造する場合巣発生性の不充分な
鋳造成型物の製造原因ともなる。
In addition, the presence of 0.2% to 2% by weight of C and/or 0.1% to 2% by weight of Mn as graphite stabilizing elements improves corrosion resistance, and also improves the heat resistance of alloyed cast iron. Therefore, it is preferable that ΔQ exists in the range of 1.5 to 4.0%.
Regarding aluminum, if more than 4.0% is added, the segregation of ΔQ or the flow of alloyed cast iron rB molten water will become poor, and for example, when casting a stalk, it may cause the production of cast moldings with insufficient cavities. .

而して、アルミニウム溶湯に対し耐食性を向上する為に
は複合合金鋳鉄組織をアルミニウムとの反応性の見られ
ない分子式Fe5Cで示されるセメンタイト地にする必
要があるが、完全なセメンタイト地もまた硬くてもろい
為に、前述のクラックが問題となる。従って、じん性を
兼ね備えたセメンタイトとフェライトの層状組織即ち、
パーライト組織とする必要がある。このパーライト組織
も出来得る限りセメンタイト地を多くし、緻密な組織と
することが耐食性の向上へとつながっている。本発明に
於いては特に上記特定の組織とすることによりこのパー
ライト地とすることが出来たものである。
Therefore, in order to improve the corrosion resistance against molten aluminum, it is necessary to make the composite alloy cast iron structure into a cementite base with the molecular formula Fe5C, which shows no reactivity with aluminum, but a completely cementite base is also hard. Because it is brittle, the cracks mentioned above become a problem. Therefore, a layered structure of cementite and ferrite that has both toughness,
It is necessary to have a pearlite structure. This pearlite structure also has as much cementite as possible to create a dense structure, which leads to improved corrosion resistance. In the present invention, this pearlite base can be obtained by particularly forming the above-mentioned specific structure.

このようにして得られた鋳鉄並びに複合合金鋳鉄はこれ
を用いてアルミニウム合金低圧鋳造用ストークにしてそ
の耐久度試験を行なった結果、連続66〜80日間の操
業において全く浸食されず原形を保持するという驚異的
記録を達成する。このことは従来知られているダクタイ
ル鋳鉄、ミーバーナイト鋳鉄、高アルミニウム鋳鉄など
の鋳鉄に属するシラール鋳鉄、クラルファー鋳鉄、アル
シロン鋳鉄などの鋳鉄、更にはTiと添加したT1鋳鉄
といえども比較できないほどの高性能なものである。
The cast iron and composite alloy cast iron thus obtained were used to make stalks for low-pressure casting of aluminum alloys, and a durability test was conducted on them. As a result, they did not erode at all during continuous operation for 66 to 80 days and maintained their original shape. achieved an astonishing record. This fact cannot be compared with conventionally known cast irons such as ductile cast iron, Mieburnite cast iron, high aluminum cast iron, etc., such as Silar cast iron, Kralfer cast iron, Alsilon cast iron, and even T1 cast iron with Ti added. It is a high-performance one.

本発明の鋳鉄並びに複合合金鋳鉄がこのような耐熱、耐
食性に優れる1つの理由として、添加物の相乗効果によ
って流電腐食を軽減させる効果の他に、溶融金属に対す
る流水性が極端に低くなるためであると考えられるがま
だ明らかではない。
One of the reasons why the cast iron and composite alloy cast iron of the present invention have such excellent heat resistance and corrosion resistance is that in addition to the effect of reducing galvanic corrosion due to the synergistic effect of additives, the water flowability for molten metal is extremely low. It is thought that this is the case, but it is not yet clear.

本発明の鋳鉄並びに複合合金鋳鉄はアルミニウム合金鋳
造用のるつぼやストークの他、銅、錫、ニッケル、亜鉛
、鉛等各種合金の金属に対しても優れた耐熱、耐久性を
有しており、これら各種溶融金属対象の素材としても有
用である。更にこの鋳鉄並びに複合合金鋳鉄は機械的性
質が良好であるので大きな利用度と経湾的効果が期待で
きるものである。
The cast iron and composite alloy cast iron of the present invention have excellent heat resistance and durability against various alloy metals such as copper, tin, nickel, zinc, and lead, as well as crucibles and stalks for aluminum alloy casting. It is also useful as a material for these various molten metal objects. Furthermore, since this cast iron and composite alloy cast iron have good mechanical properties, they can be expected to have great utility and economical effects.

以下、実施例により本発明を具体的に説明する。Hereinafter, the present invention will be specifically explained with reference to Examples.

但し下記例に於いて部とあるのは重量部を示す。However, in the following examples, parts indicate parts by weight.

実施例1 キューボラ炉投入時点における配合量は参罰材60部、
新鋭30部、コークス15部、石灰石10部であり、こ
の配合量に対してチタン酸カリウム5部とベントナイト
0.6部とを水で混線、塊状に成型し、乾燥したものを
上記配合物と共に炉頂に添加した。キューポラでの溶解
条件は溶解温度が1550℃以上1800℃までどし、
出湯温度1580℃である。かくして得られた溶湯を前
炉にとり、該溶湯100部に対しホウ酸す1〜ツリウム
部を添加し、饅込み温度1520℃で鋳造した。
Example 1 The blending amount at the time of charging into the Cubola furnace was 60 parts
30 parts of Shinryu, 15 parts of coke, and 10 parts of limestone.To this amount, 5 parts of potassium titanate and 0.6 parts of bentonite are mixed with water, molded into a lump, dried, and combined with the above mixture. Added to the top of the furnace. The melting conditions in the cupola are such that the melting temperature is from 1550℃ to 1800℃,
The hot water temperature is 1580°C. The thus obtained molten metal was placed in a forehearth, 1 to thulium part of boric acid was added to 100 parts of the molten metal, and cast at a pouring temperature of 1520°C.

実施例2 キューボラ炉投入時点における配合量は鋼材60部、新
鋭30部、故銑10部、フェロシリコン15部、コーク
ス13部、石灰石10部でありこの配合量に対してチタ
ン酸カリウム6部とベントナイト0.7部とを水で混練
、塊状に成型し、乾燥したものを上記配合物と共に炉頂
に添加した。
Example 2 The blended amounts at the time of charging into the Cubola furnace were 60 parts of steel, 30 parts of new metal, 10 parts of waste pig iron, 15 parts of ferrosilicon, 13 parts of coke, and 10 parts of limestone. 0.7 part of bentonite was kneaded with water, formed into a lump, dried, and added to the top of the furnace together with the above blend.

キューポラ溶解条件は実施例1と同じにした。またホウ
酸す1〜シリウム部に代えフェロホウ素2.5部(但し
Fe9100部に対し)を使用しlこ 。
The cupola melting conditions were the same as in Example 1. Also, 2.5 parts of ferroboron (for 9100 parts of Fe) was used in place of 1 part to silium of boric acid.

実施例3 実施例1と同じ方法で実施した。配合量は鋼材60部、
新鋭40部、コークス15部、故銑2.5部、フェロシ
リコン10部、フェロクロム2部、フェロホウ素2部、
チタン酸リチウム5部及びベントティl−0,6部(F
e9100部に対して)であった。
Example 3 It was carried out in the same manner as in Example 1. The blending amount is 60 parts of steel,
40 parts of new technology, 15 parts of coke, 2.5 parts of waste iron, 10 parts of ferrosilicon, 2 parts of ferrochrome, 2 parts of ferroboron,
5 parts of lithium titanate and 0.6 parts of bentoti (F
e9100 copies).

実施例4 実施例1で製造された溶湯の一部を前炉に取り、溶湯1
00部に対してあらかじめ別の炉で溶解させておいた純
アルミニウム5部を添加、鋳型に鋳造した。
Example 4 A part of the molten metal produced in Example 1 was taken into the forehearth, and molten metal 1
00 parts, 5 parts of pure aluminum, which had been previously melted in a separate furnace, was added and cast into a mold.

実施例5 実施例2で製造された溶湯の一部を取り、溶湯100部
に対し、糺アルミニウム3部を添加鋳造した。
Example 5 A portion of the molten metal produced in Example 2 was taken and cast by adding 3 parts of fused aluminum to 100 parts of the molten metal.

実施例6 実施例3で@造された溶湯を前炉に取り、??J渇10
0部に対して、あらかじめ別の炉で溶解さVておいた純
アルミニウム4部を添加鋳造した。
Example 6 The molten metal produced in Example 3 was taken into the forehearth and ? ? J thirst 10
To 0 parts, 4 parts of pure aluminum, which had been previously melted in a separate furnace, was added and cast.

実施例1〜6を用いてアルミニウム合金低圧鋳造用スト
ークを試作した。このストークの千ωをあらかじめ測定
した。また一方比較例に使用づ−るためにFe12のス
トークを鋳込む。このスト−クは30.2kaであった
。それぞれ低圧鋳造装置にセラ1〜し、アルミニウム合
金鋳造の操業によって本発明の鋳鉄とFCストークの耐
熱、耐久、耐腐食性について連続操業試験を行なった。
Stokes for low-pressure casting of aluminum alloys were prototyped using Examples 1 to 6. The 1,000 ω of this stalk was measured in advance. On the other hand, a stalk of Fe12 was cast for use in a comparative example. This stroke was 30.2 ka. Continuous operation tests were conducted on the heat resistance, durability, and corrosion resistance of the cast iron and FC stalk of the present invention by using aluminum alloy casting operations in a low-pressure casting apparatus.

結果を第1表に示す。The results are shown in Table 1.

手続補1[:書(内′ら) 昭ft+59年 4月 6I1 昭和58年 特 許 願第 155827 +j26発
明の名称 合金鋳鉄 3、袖11ヨをする:バ 事件との関係 特許出願人 大塚化学薬品株式会社 4、代理 人 大阪市東区SP−町町2())10 II<の鶴[ル1
1・、11・06−2(X(−0!■(代)(652]
’l 弁理士 三 技 英 二”””’x 5、補正命令の[1イJ 、: 自発 6 補正により増加する発flj]の数明細zJ)中発
明の、i14細な説明の項8 補正の内容 補 正 の 内 容 1 明8いロ11第6頁第6行「2゜5〜4〜0」とあ
るを「2゜5〜4.0」と訂正する。
Supplementary Procedures 1 [: Book (inside) April 1977 6I1 1981 Patent Application No. 155827 +j26 Name of invention Alloy cast iron 3, sleeve 11 yo: Relationship with Ba case Patent applicant Otsuka Chemicals Co., Ltd. 4, Agent SP-Machicho 2 (), Higashi-ku, Osaka 10 II < Tsuru [Le 1
1., 11.06-2(X(-0!■(generation)(652)
'l Patent Attorney 3 Waza Eiji"""'x 5. Specification of the number of [1 i J,: Voluntary 6 Increasing expression flj] of the amendment order ZJ) Invention, i14 Detailed Explanation Section 8 Amendment Contents Correction Contents 1. 8-B-11, page 6, line 6, ``2°5-4-0'' is corrected to ``2°5-4.0''.

(以 上)(that's all)

Claims (1)

【特許請求の範囲】 ■ 鋳鉄溶湯に、チタン酸アルカリ金属塩とホウ素化合
物とを添加して成る合金鋳鉄。 ■ 鋳鉄溶湯に、チタン酸アルカリ金is、ホウ素化合
物及びアルミニウムを添加して成る複合合金鋳鉄。
[Claims] ■ An alloy cast iron made by adding an alkali metal titanate and a boron compound to molten cast iron. ■ Composite alloy cast iron made by adding alkali gold titanate, boron compounds, and aluminum to molten cast iron.
JP15582783A 1983-08-25 1983-08-25 Alloy cast iron Granted JPS6050144A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15582783A JPS6050144A (en) 1983-08-25 1983-08-25 Alloy cast iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15582783A JPS6050144A (en) 1983-08-25 1983-08-25 Alloy cast iron

Publications (2)

Publication Number Publication Date
JPS6050144A true JPS6050144A (en) 1985-03-19
JPH0565575B2 JPH0565575B2 (en) 1993-09-20

Family

ID=15614355

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15582783A Granted JPS6050144A (en) 1983-08-25 1983-08-25 Alloy cast iron

Country Status (1)

Country Link
JP (1) JPS6050144A (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56142848A (en) * 1980-01-25 1981-11-07 Nordstjernan Rederi Ab Abrasion resistant cast iron
JPS5814867A (en) * 1981-07-21 1983-01-27 Canon Inc Developing device
JPS58151450A (en) * 1982-02-27 1983-09-08 Kyowa Chuzosho:Kk Composite alloy cast iron
JPS58155828A (en) * 1982-03-12 1983-09-16 株式会社日立製作所 Electric cleaner
JPS58155829A (en) * 1982-03-12 1983-09-16 株式会社日立製作所 Electric cleaner
JPS5993852A (en) * 1982-11-20 1984-05-30 Kyowa Chuzosho:Kk Composite alloy cast iron

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56142848A (en) * 1980-01-25 1981-11-07 Nordstjernan Rederi Ab Abrasion resistant cast iron
JPS5814867A (en) * 1981-07-21 1983-01-27 Canon Inc Developing device
JPS58151450A (en) * 1982-02-27 1983-09-08 Kyowa Chuzosho:Kk Composite alloy cast iron
JPS58155828A (en) * 1982-03-12 1983-09-16 株式会社日立製作所 Electric cleaner
JPS58155829A (en) * 1982-03-12 1983-09-16 株式会社日立製作所 Electric cleaner
JPS5993852A (en) * 1982-11-20 1984-05-30 Kyowa Chuzosho:Kk Composite alloy cast iron

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