JPS59130644A - Mold coating material for furan resin casting mold - Google Patents

Mold coating material for furan resin casting mold

Info

Publication number
JPS59130644A
JPS59130644A JP409283A JP409283A JPS59130644A JP S59130644 A JPS59130644 A JP S59130644A JP 409283 A JP409283 A JP 409283A JP 409283 A JP409283 A JP 409283A JP S59130644 A JPS59130644 A JP S59130644A
Authority
JP
Japan
Prior art keywords
mold
coating material
casting
sulfurization
slag
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
JP409283A
Other languages
Japanese (ja)
Other versions
JPS6125453B2 (en
Inventor
Takeo Matsuda
松田 健男
Kazuyuki Kurisu
栗栖 一之
Masahiro Tada
昌弘 多田
Ikuo Kuroki
黒木 郁夫
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 Yakin Kogyo Co Ltd
Original Assignee
Nippon Yakin Kogyo Co 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 Nippon Yakin Kogyo Co Ltd filed Critical Nippon Yakin Kogyo Co Ltd
Priority to JP409283A priority Critical patent/JPS59130644A/en
Publication of JPS59130644A publication Critical patent/JPS59130644A/en
Publication of JPS6125453B2 publication Critical patent/JPS6125453B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C3/00Selection of compositions for coating the surfaces of moulds, cores, or patterns

Abstract

PURPOSE:To prevent carburization and sulfurization of an alloy casting and to obtain a good casting surface by incorporating the slag formed in the reduction period of a steel making stage at a specific ratio in the entire aggregate as an aggregate constituting component of a mold coating material for a furan resin casting mold. CONSTITUTION:The slag formed in the reduction period of a steel making stage is added at 5-40% in the entire aggregate as an aggregate constituting component for a commercially marketed zircon mold coating material used for a furan resin casting mold, and the aggregate is adjusted to about 60 Be<-> in I.P.A. The slag is formed in the reduction period in melting a stainless steel, heat resisting steel or carbon steel and consists of about 15-40% SiO2, 40-60% CaO, <=10% MgO, <=3% FeO and others and the basicity thereof is in a range of about 1.2- 3.8. The above-mentioned mold coating material is coated on a self-curing casting mold of furan and after the mold is dried with a burner, a desired corrosion and heat resistant alloy is cast therein. The carburization and sulfurization of the alloy casting are thus effectively prevented and the good casting surface is obtd.

Description

【発明の詳細な説明】 本発明は、合金鋳造品製造の際に用いられるフラン樹脂
鋳型用塗型材に関するものであり、特に本発明は、製造
される合金鋳造品の浸炭、浸硫を有効に防止することの
できるフラン樹脂鋳型用塗型材に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coating material for furan resin molds used in the production of alloy castings. The present invention relates to a coating material for furan resin molds that can prevent the above problems.

フラン樹脂とスルホン酸系硬化剤がボンドとして一般に
月いられているフラン樹脂鋳型は高い生産性と古砂の回
収、再生が容易であることなどの擾れた%徴を有するた
め近年多く使用されている。
Furan resin molds, in which furan resin and a sulfonic acid curing agent are generally used as a bond, have been widely used in recent years because they have excellent productivity characteristics such as high productivity and easy recovery and recycling of old sand. ing.

しかし、フラン樹ハ17鋳型は注湯することにより樹脂
、硬化剤が熱分解し、Go + 002 + CH4あ
るいlは5O2TH2S等のC系IS系のガスが発生す
るため鋳造品の表面には、浸炭、浸硫による異常層が生
成するという問題があった。
However, when the Furanjuha 17 mold is poured, the resin and curing agent are thermally decomposed and C-based IS-based gases such as Go + 002 + CH4 or 5O2TH2S are generated. There was a problem that abnormal layers were formed due to carburization and sulfurization.

合金鋳造品において、この異常層の存在は、そ・の用途
の上から有害であることはもちろんであシ、また鋳造品
の製造時においても割れ等の欠陥の発生原因となるため
有害である。
The presence of this abnormal layer in alloy castings is not only harmful from the standpoint of its intended use, but also harmful as it causes defects such as cracks during the manufacturing of castings. .

この異常層の発生、すなわち浸炭、浸硫の防止対策とし
て従来、以下のような公知の方法があるさく1)  ′
&Jj物砂として、クロマイト砂を用いる方法。
As a measure to prevent the occurrence of this abnormal layer, that is, carburization and sulfurization, there are conventionally known methods such as the following1)'
&Jj A method of using chromite sand as material sand.

(2)鋳物砂中へFe2O3を添加する方法。(2) A method of adding Fe2O3 to foundry sand.

(3)塗型材中へFe2O3あるいはN1.へ法等の各
種酸化物を添加する方法。
(3) Fe2O3 or N1. A method of adding various oxides, such as the hexamethod.

(4)塗型拐として2CaO−8102とG aGo 
3の混合物゛を用いる方法、あるいは塗型中に(Ea、
Go3を添加する方法。
(4) 2CaO-8102 and GaGo as coating molds
A method using a mixture of (3) or (Ea,
Method of adding Go3.

(5)操業の管理(87M比、 L、O,■、樹脂・硬
化剤添加二量の制限など)による方法(綜合鋳物センタ
ー:有機自硬性鋳型における鋳造欠陥とその−゛′対策
事例 昭和37年3月 P−/?)。
(5) Methods of operation management (87M ratio, L, O, ■, limits on the amount of resin and curing agent added, etc.) (General Foundry Center: Examples of casting defects in organic self-hardening molds and their countermeasures 1962) March P-/?).

しかしながら、これらの方法は以下の点で問題があり、
必ずしも一般的ではなく、効果も不充分である。
However, these methods have the following problems:
It is not necessarily common and its effects are insufficient.

すなわち、(1)の方法によれば、クロマイト砂が高価
であること、クロマイト砂の比重が大きいこと、クロマ
イト砂にけい砂が混入すると燐量発生の原因となること
(例えは、銘木ら;鋳物vol。
That is, according to method (1), chromite sand is expensive, chromite sand has a high specific gravity, and mixing silica sand with chromite sand causes generation of phosphorus (for example, Meiki et al.; Casting vol.

yり(/デフ、2)JIG乙 P、7g 、 P、 /
? )などから、鋳物砂を高価なりロマイト砂に変塑す
る場合はクロマイト砂の比重が大きいため、場合によっ
ては設備変更が必要となり、さらには操業条件を新たに
設定することも必要となる@製造コストの増加につなが
る。また肌砂のみにクロマイト砂を使用する場合には、
砂再生のだめクロマイト砂と他の砂とを分離する設備が
必要となる。
yri (/def, 2) JIG Otsu P, 7g, P, /
? ), etc., when converting foundry sand into expensive chromite sand, the specific gravity of chromite sand is high, so in some cases it may be necessary to change equipment, and it may also be necessary to set new operating conditions. leading to increased costs. In addition, when using chromite sand only for skin sand,
Equipment for separating chromite sand from other sands is required for sand regeneration.

(2)の方法によれば、F’5203の添加によシ鋳製
強度が劣化・するため必ずしも実用的とはいえない(綜
合鋳物センター:有機自硬性鋳型における鋳造欠陥とそ
の対策事例(その−1) 昭和57年3月□・P、g−
9)。
According to method (2), the casting strength deteriorates due to the addition of F'5203, so it is not necessarily practical. -1) March 1981 □・P, g-
9).

(3)の方法によれば、後述するように添加量が少ない
と浸炭′・浸硫の防止効果がなく、また添加量が多いと
鋳肌外観が不良となる。
According to method (3), as will be described later, if the amount added is small, there is no effect of preventing carburization and sulfurization, and if the amount added is too large, the cast surface appearance will be poor.

(4)の方法によれば、浸炭・浸硫の防止効果が必ずし
も充分とはいえない(津田ら;鋳物r/(/qtt)q
、!;/9および津田ら;鋳物53(/灯/)、!+ 
12−27)。
According to method (4), the effect of preventing carburization and sulfurization is not necessarily sufficient (Tsuda et al.; Casting r/(/qtt)q
,! ;/9 and Tsuda et al.; Casting 53 (/light/),! +
12-27).

本発明は、上記のような従来方法における問題点を生じ
ることなしに、フラン樹脂鋳型を使用したときの合金鋳
造品への浸炭・浸硫を効果的に防止することができる塗
型材を提供することを目的とするものである。
The present invention provides a coating material that can effectively prevent carburization and sulfurization of alloy castings when using furan resin molds without causing the problems of conventional methods as described above. The purpose is to

す々わち本発明は、合金鋳造品製造の際に用いられるフ
ラン樹脂鋳型用塗型材において塗型材中の骨材の構成成
分として、製鋼工程の還元期で生成するスラグを全骨材
中に9〜aO%含有させて々ることを特徴とするフラン
樹脂鋳型用塗型材に関するものである。
In other words, the present invention uses slag produced during the reduction stage of the steelmaking process as a constituent component of the aggregate in the coating material for furan resin molds used in the production of alloy casting products. The present invention relates to a coating material for furan resin molds, characterized in that it contains 9 to aO%.

本発明塗型材は、フラン樹脂鋳型を使用して合金鋳造品
を製造するにあたシ、従来方法のように″□鋳物砂の変
更、造型方法の変更等、既存の操業方法を変更する必要
なしに、前述のように単に塗型材中にスラグを加えるだ
けで容易に実施できるものであり、これによりフラン樹
脂鋳型使用に起因する浸炭・浸硫を従来になく効果的に
防止することができる。
The mold coating material of the present invention does not require changes to existing operating methods such as changing the molding sand or changing the molding method, unlike conventional methods, when producing alloy castings using furan resin molds. This can be easily done by simply adding slag to the coating material as described above, and this can more effectively prevent carburization and sulfurization caused by the use of furan resin molds than ever before. .

なお塗型の主な機能は正常f1.鋳肌外歓を得ることに
あるが、本発明の塗型材を使用しても上記機能は完全に
、達成され、この点においても従来の塗型材ならびに方
法と異なっている。
The main function of the coating mold is normal f1. The objective is to obtain a cast surface appearance, and the above-mentioned functions are completely achieved even when using the mold coating material of the present invention, and this point also differs from conventional mold coating materials and methods.

以下、本発明について詳細に説明する。The present invention will be explained in detail below.

合金鋳造品の鋳込湿(9)は/!;gO〜/6θθ°C
と比較的高温であり、浴湯の砂粒間への浸透や、鋳肌へ
の砂粒の燐量が発生しやすい。そのため鋳肌外観。
The casting humidity (9) of alloy castings is /! ;gO~/6θθ°C
This relatively high temperature makes it easy for the bath water to penetrate between the sand grains and for the amount of phosphorus in the sand grains to reach the casting surface. Therefore, it has a cast surface appearance.

鋳造品品質等の点から塗型が必要となる。したがって浸
炭・浸硫を塗型のみにより防止することができれば、既
存の鋳物製造方法を変更することなしに正常な鋳物の製
造が可能である。
Coating molds are required from the standpoint of casting quality. Therefore, if carburization and sulfurization can be prevented using only the coating mold, normal castings can be manufactured without changing the existing casting manufacturing method.

そこで、まず浸炭・浸竹のUj止効果が知られている公
知の添加剤を重いのジルコン系塗型材に添加して、これ
らの添加剤の性能を実際に評価する”ため鋳造試験を行
った。この試験は第1表に示す鋳造条件により行ったも
ので、第2表にその結果を示す。
Therefore, we first added known additives that are known to have a Uj-stopping effect during carburizing and bamboo soaking to a heavy zircon-based coating material, and conducted a casting test to actually evaluate the performance of these additives. This test was conducted under the casting conditions shown in Table 1, and the results are shown in Table 2.

第1表 鋳  型;フラン自硬性鋳型 鋳型砂;再生砂(ジルコン砂とけい砂の混合砂)鋳fl
HfAk ; JIS G5/、2/ A号試験片塗型
材;市販のジルコン塗型材に各種添加剤を加え、1.P
、Aで約t、o B−に調整塗型塗布;ハケ塗り、バー
ナ乾燥 鋳込MUlf ; SC8/、y (溶湯成分C: 0
.OA%。
Table 1 Mold; flan self-hardening mold molding sand; recycled sand (mixed sand of zircon sand and silica sand) casting fl
HfAk; JIS G5/, 2/ A test piece coating material; various additives were added to a commercially available zircon coating material; 1. P
, A to approximately t, o B- Adjustment coating application; Brush coating, burner dry casting MUlf; SC8/, y (Molten metal composition C: 0
.. OA%.

S二〇、θo4t%) 鋳込温度; /sgo −1too℃ 第2表 備考 そ:塗型骨材中の添加剤の含有重量(%)0 :
分析しなかったので含有量不明のもの15販のジルコン
系塗型材は、ジルコンフラワーを骨材として、有機粘結
剤、有機相合剤、 1.P、A(イソプロピルアルコー
ル)からなるもので、塗□型材への各種添加剤の添加量
は、塗型骨材中の含有量が第−表の値(%)となるよう
に添加した。いずへの添加剤を単独又)は複合で添加し
た場合も浸炭あるいは浸硫が認められ、また鋳肌外観が
損なわれており、浸炭・浸硫防止効果が不充分であった
り、塗型材本来の機能を失なっていることは明らかであ
る。
S20, θo4t%) Casting temperature; /sgo -1too℃ Table 2 Notes: Content weight (%) of additives in the coating aggregate 0:
The content is unknown because it was not analyzed.15 The commercially available zircon-based coating material uses zircon flour as an aggregate, an organic binder, an organic compatibilizer, and 1. It consists of P and A (isopropyl alcohol), and the amounts of various additives added to the painted □ mold material were such that the content in the painted mold aggregate was the value (%) shown in Table 1. Carburization or sulfurization is observed even when additives (either singly or in combination) are added, and the appearance of the cast surface is impaired, and the carburization and sulfurization prevention effect is insufficient, and the coating material It is clear that it has lost its original function.

すなわち、フラン樹脂鋳型は注湯により樹脂硬化剤が熱
分解するため鋳型内は還元性雰囲気とな1゛る。したが
って酸素供給源であるFe2O2の添加は、雰囲気を酸
化性にすることについては有効であシ、実際この試験に
おいても市販のジルコン系塗型(添加剤なし)を塗布し
た場合に比べ酸化スケールの発生貝に増加が認められた
。しかし、第コ表□に示したように添加量が少ない場合
には、鋳物表面スケール内部までOのポテンシャルを高
くすることができず、もともとC2Sのポテンシャルが
高い鋳型的雰囲気のため、浸炭・浸硫の防止効果が充分
認められない。他方、Fe2O2の添加量を多”、<シ
た場合は、同表に示すとおシ鋳肌面の外観が不良となシ
、この面から、実際の生産に適用することができない。
That is, in the furan resin mold, the resin curing agent is thermally decomposed by pouring, so the inside of the mold becomes a reducing atmosphere. Therefore, the addition of Fe2O2, which is an oxygen supply source, is effective in making the atmosphere oxidizing, and in fact, in this test, the oxide scale was lower than when a commercially available zircon coating (without additives) was applied. An increase was observed in the number of spawned shellfish. However, when the amount of addition is small as shown in Table □, it is not possible to increase the O potential to the inside of the casting surface scale, and the mold atmosphere has a high C2S potential to begin with, resulting in carburizing and oxidation. The effect of preventing sulfur is not sufficiently recognized. On the other hand, if the amount of Fe2O2 added is too large, the appearance of the casting surface will be poor as shown in the same table, and from this point of view it cannot be applied to actual production.

また他の添加剤すなわちCaO+ CaCO3あるいは
それらとFe2O2と相合して添加した場合についても
浸炭・浸硫防止効果が不充分、あるいは鋳肌外観や品質
が不充分で同様に実際の生産に適用できない。そこで、
ステンレス鋼#4@品に対する浸炭・浸硫を充分防止す
ることができる塗型材を開発することを目的として、新
たに有効な塗型添加剤について種々検討したところ、製
鋼工程における還元期に生成するスラlが、浸炭・浸硫
の充分な防止に有効であることを知見した。またこのス
ラグを添加した塗型材の性能を、他の鋳造品すなわち耐
熱鋼、耐食耐熱合金等について調査したところ、ステン
レス鋼と同様、浸炭、浸硫を有効に防止し、良好な鋳肌
外観が得られることが確認された。
Furthermore, when other additives, such as CaO+CaCO3 or a combination thereof with Fe2O2, are added, the effect of preventing carburization and sulfurization is insufficient, or the appearance and quality of the cast surface are insufficient, so that they cannot be applied to actual production. Therefore,
With the aim of developing a coating material that can sufficiently prevent carburization and sulfurization on stainless steel #4, we investigated various new effective coating additives and found that they are formed during the reduction stage of the steelmaking process. It has been found that slurry is effective in sufficiently preventing carburization and sulfurization. In addition, we investigated the performance of mold coating materials with this slag added to other casting products, such as heat-resistant steel, corrosion-resistant heat-resistant alloys, etc., and found that, like stainless steel, it effectively prevents carburization and sulfurization, and provides a good cast surface appearance. It has been confirmed that it can be obtained.

本発明塗型材の内容をさらに明確にするため、′−に行
つた試験結果の一部を用いて以下に説明す□る。
In order to further clarify the contents of the mold coating material of the present invention, some of the test results conducted in 1-- will be explained below.

第3表は鋳造条件、第9表は試験に用いたスラグの成分
分析値を示す。
Table 3 shows the casting conditions, and Table 9 shows the component analysis values of the slag used in the test.

第   3  表 鋳  型;フラン自硬性鋳型 鋳型砂;再生砂、ジルコン砂、けい砂。Table 3 Mold: Furan self-hardening mold Molding sand; recycled sand, zircon sand, silica sand.

クロマイト砂 鋳型形状; JIS Cr5i21A号試験片塗 型材
;市販のジルコン系塗型材にスラグを添加し1.P、A
にて約6゜8石に調整年塗型塗布;ハケ塗り 鋳込鋼fg : SO8s (o、o、5′%G r 
0−ttub 7゜(成分、@/りgo −/goo 
’C)適温度)SC8/、O(o、o□C、0,001
1%S。
Chromite sand mold shape: JIS Cr5i21A test piece coating Mold material: Slag was added to a commercially available zircon-based mold material.1. P, A
Adjusted to approx. 6° 8 stones at 100 yen; Brush-coated cast steel fg: SO8s (o, o, 5'%G r
0-ttub 7゜(component, @/rigo -/goo
'C) Suitable temperature) SC8/, O (o, o□C, 0,001
1%S.

isgθ−/A00℃) SCH/、3(o、、yo%G 、 o、oot%s。isgθ-/A00℃) SCH/, 3(o,, yo%G, o, oot%s.

l左10−/りti、o℃) ハステロイC(o、oq%c、 o、ooq%S。l left 10-/riti, o℃) Hastelloy C (o, oq%c, o,ooq%S.

/グso℃) 14E q表中λ/〜7のスラグは、ステンレス鋼、・
耐熱鋼又は炭素鋼の溶解の還元期、すなわち製鋼工程の
還元期に生成されたもので、成分的には5102約/j
 〜lIO%、CaO/1.θ〜60%、 MgO10
%以下。
/gso℃) 14Eq The slag with λ/~7 in the table is stainless steel,
It is produced during the reduction period of melting heat-resistant steel or carbon steel, that is, during the reduction period of the steelmaking process, and its composition is approximately 5102/j
~lIO%, CaO/1. θ~60%, MgO10
%below.

FeOJ%以下、その他からなり、塩基度はへコ〜JJ
の範囲内である。Agのスラグけ、N1精錬時に生成す
るもので比較のため用いたものである。
Consisting of less than FeOJ% and others, basicity is low ~ JJ
is within the range of This Ag slag is produced during N1 refining and was used for comparison.

これらのスラグを市販のジルコン系塗型材(ジルコノフ
ランが骨材で、有機粘結剤、有機相合剤を含む1.P、
Aを溶剤としたもの)に添加して工、P、Aを加え約b
o B≦に潤整後、フラン自硬性鋳型に塗布しバーナー
乾燥後各種合金を鋳込んだ。第5表はその結果であり、
第1I表のA/〜gのスラグを塗型材骨相中に種々の含
有量となるように加えた場合の各種合金鋳造品切肌面の
分析結果と外観評価゛□結果を示す。
These slags were mixed with a commercially available zircon-based coating material (Zirconofuran is the aggregate and contains an organic binder and an organic compatibilizer.
A is used as a solvent), and then P and A are added to make about b
o After moisturizing to B≦, it was applied to a furan self-hardening mold, and after drying with a burner, various alloys were cast. Table 5 shows the results.
The results of analysis and appearance evaluation of the cut surface of various alloy castings when various contents of slag A/~g in Table 1I are added to the skeleton of the coating material are shown.

第5表よシスラグ含有量が3%の場合鋳肌面の成分はC
は0.10%以上、Sは0.02θ%超えと浸炭・浸硫
により増加していることがわかる。この試料の鋳肌断面
の顕微鏡写真を第1図に示す。
Table 5: When the cislag content is 3%, the component of the cast surface is C.
is 0.10% or more, and S is more than 0.02θ%, which shows that they increase due to carburizing and sulfurizing. A microscopic photograph of the cross section of the casting surface of this sample is shown in FIG.

SO8/3の規格によればSは0.0ダ0%以下である
が・浸硫によって本試料のようにSiが増加した場合に
は、fiJj肌而の一面に硫化物が集中して認められる
。このような鋳肌面にTIG溶接を行うと、HAZ割れ
あるいはビードタテ割れが発生する場合があった。そこ
で、分析値的にcj:浸硫が認められるが、顕微鏡的に
集中した硫化物が実際上認められないSが0.020%
以下の範囲を浸硫が防止された鋳肌と判定した。池の合
金切遺品についても同様の方法により判定した。
According to the SO8/3 standard, S is 0.0% or less, but when Si increases as in this sample due to sulfurization, sulfide is concentrated on one side of the skin. It will be done. When TIG welding is performed on such a cast surface, HAZ cracking or vertical bead cracking may occur. Therefore, cj: sulfurization is recognized in terms of analytical values, but S is 0.020%, where concentrated sulfides are not actually recognized microscopically.
The following range was determined to be a cast surface in which sulfurization was prevented. Ike's alloy relics were also evaluated using the same method.

浸炭について(rl、 S’ SC8/3の場合正常な
顕微鏡組゛織(オーステナイトとδフェライトのコ相組
織)が鋳肌面で消失してオーステナイト単相となシ、そ
の層の厚さがQ、2myh程度以上存在し、部分的に点
状の炭化物が認められたものが本試験においてはCは0
010%以上であったため、鋳肌面分析値はCが0.1
0%未隣の範囲を浸炭が防止された鋳肌と判定した。ス
ラグ含有量3%の場合は、浸炭並びに4硫によシ鋳肌面
の品質が劣化し、一方スラグ含有量が5%の場合は浸炭
I浸硫ともに上記の分析値より低く、かつ鋳肌外観も良
好であった。そこで本発明におけるスラグ含有量は下限
を5%とする。
Regarding carburization (rl, S' In the case of SC8/3, the normal microscopic structure (co-phase structure of austenite and δ ferrite) disappears on the casting surface and becomes a single phase of austenite, and the thickness of that layer is Q. , 2 myh or more, and where point-like carbides were partially observed, C was 0 in this test.
0.010% or more, the cast surface analysis value was 0.1.
The range below 0% was determined to be a cast surface in which carburization was prevented. When the slag content is 3%, the quality of the cast surface surface deteriorates due to carburization and 4-sulfurization, while when the slag content is 5%, both carburization and sulfurization are lower than the above analytical values, and the quality of the cast surface surface is lower than the above analysis value. The appearance was also good. Therefore, the lower limit of the slag content in the present invention is set to 5%.

次にスラグ含有量が乙5%の場合は第5表に示すSO8
/、?の場合のように鋳肌外観が劣化することが判り、
一方スラグ含有鼠がlIO%の場合は浸炭。
Next, if the slag content is Otsu 5%, SO8 shown in Table 5
/,? It was found that the cast surface appearance deteriorated as in the case of
On the other hand, if the slag content is lIO%, carburization is performed.

浸硫ともに上記の分析値より低く、かつ鋳肌外観も良好
なのでスラグ含有量の上限をtio%とする。
Both sulfurization values are lower than the above analysis values, and the cast surface appearance is good, so the upper limit of the slag content is set at tio%.

以上によシ本発明塗型材は、塗型材骨材含有量として全
骨材中に5〜グθ%含有させると浸炭、浸硫を有効に防
止し良好な鋳肌外観が得られる。
In view of the above, in the mold coating material of the present invention, when the mold coating material aggregate content is 5 to θ% in the total aggregate, carburization and sulfurization can be effectively prevented and a good casting surface appearance can be obtained.

またスラグの種類′についてみると、第5表に示すと2
すA/〜7のスラグではいずれも鋳肌面の分析1直並び
に鋳肌外観評価の結果は良好であシ、本発明の塗型材の
機能を充分満たすものである。
Regarding the types of slag, Table 5 shows that there are 2 types of slag.
All of the slags A/ to 7 had good results in the first analysis of the casting surface and the evaluation of the appearance of the casting surface, and fully satisfied the function of the mold coating material of the present invention.

なお、ila gの1′IT1精錬よシ得られた還元性
のスラグは、浸炭、浸硫防止効果が認められない。
Incidentally, the reducing slag obtained by the 1'IT1 refining of ilag has no effect of preventing carburization and sulfurization.

次に、スラグの粒度について試験を行い検討した結果を
第6表に示す。鋳込条件は第3表と同一である(たソし
溶湯成分だけ異なる)。
Next, the particle size of the slag was tested and the results are shown in Table 6. The casting conditions are the same as in Table 3 (only the molten metal composition differs).

/ 第4表の結果より、粒度が10θメツシュ以上の細か込
スラグは、本発明塗型材骨材として充分有効であること
がわかる。
/ From the results in Table 4, it can be seen that finely packed slag with a particle size of 10θ mesh or more is sufficiently effective as an aggregate for the mold coating material of the present invention.

以上、本発明塗型材の検討結果について述べたが、従来
、塗型材の骨材としては、燐量の防止など鋳肌外観不良
を防止する観点から、充分な耐火度が必要であると考え
られていた。
The above has described the study results for the mold coating material of the present invention. Conventionally, it has been thought that the aggregate for the mold coating material needs to have sufficient fire resistance from the viewpoint of preventing poor casting surface appearance, such as by preventing the amount of phosphorus. was.

これに反し、本発明塗型材は、耐火度が比較的低い製鋼
工程の還元期で生成するスラグを塗型材の骨材g酸成分
としながら塗型材本来の機能を損なわず、フラン樹脂鋳
型による浸炭・浸硫を従来になく防止できる。
On the other hand, the mold coating material of the present invention uses slag produced during the reduction stage of the steelmaking process, which has a relatively low fire resistance, as the aggregate g acid component of the mold coating material, without impairing the original function of the mold coating material, and by carburizing using a furan resin mold. - Sulfurization can be prevented like never before.

次に本発明の塗型材を実施例について説明する。Next, examples of the mold coating material of the present invention will be described.

実施例1 7辺が100mmの立方体(押湯 径/ 0.?)φ闘
、高さ100 mm )のフラン樹脂鋳型(再生砂)に
、市販のジルコン塗型材と、本発明塗型材(第9表の煮
/のスラグとジルコン塗型材を/:9の割合で混合し、
有機粘結剤、界面活性剤、沈降防止剤等を骨材重置に対
しそれぞれ5%、0.3%、3%加え、水で約りθBコ
に調整したもの)とを別々に塗布しζSUS 32q 
J を相当のステンレス鋼溶湯を鋳込温度it、oo℃
で鋳込んだ。得られた鋳造品の鋳肌各部断断面の顕微鏡
組織(村上氏試薬エツチング)を第、2図(イ)、(ロ
)に示す。第2図(イ)は本発明塗型材を施し、た部分
における鋳肌であり、これをみると、正常な本鋼種の組
織を示しており、顕微鏡組織的に、浸炭、浸硫は全く認
めらねない(なお一部の黒色部分はσ相である)。
Example 1 A commercially available zircon coating material and a coating material of the present invention (no. 9 Mix the slag and zircon coating material in the ratio of /:9,
5%, 0.3%, and 3% of organic binder, surfactant, anti-settling agent, etc. were added to the aggregate, and the mixture was adjusted to θB with water and applied separately. ζSUS 32q
J is equivalent to the casting temperature of molten stainless steel it, oo℃
It was cast in The microscopic structure (etched with Murakami's reagent) of each part of the casting surface of the obtained casting is shown in Figures 2 (a) and 2 (b). Figure 2 (a) shows the casting surface of the part coated with the coating material of the present invention, which shows the normal structure of this steel, and microscopically, no carburization or sulfurization was observed. (Note that some black parts are in the σ phase).

これに対し、第2図(ロ)は市販のジルコン塗型材を施
した部分における鋳肌であり、7ラン樹脂鋳型からの浸
炭のため、組織が変化し、地がオーステナイトC白色部
)とな探、フェライトとオーステナイトの比率が逆転し
ている。減少したフェライト中には浸炭による炭化物が
認められ、写真では淡黒色となってみえる。
On the other hand, Figure 2 (b) shows the casting surface of a part coated with a commercially available zircon coating material. Due to the carburization from the 7-run resin mold, the structure has changed and the base is austenite C (white part). The ratio of ferrite and austenite is reversed. Carbide due to carburization is observed in the reduced ferrite, which appears pale black in the photo.

また濃黒色部は浸硫によシ生成した硫化物がエツチング
によって腐食され溝状になったものである。
The dark black areas are groove-like grooves formed by etching of sulfides produced during sulfurization.

このように、市販のジルコン塗型材を施した鋳肌には異
常層が深さハ5an程度まで認められた。
As described above, an abnormal layer was observed up to a depth of approximately 5 ann on the casting surface coated with a commercially available zircon coating material.

実施例2 それぞれ異なる塗型を施したフラン樹脂鋳型(ジルコン
砂)を用いてSC81,3のボール弁を鋳造した。フラ
ン樹脂鋳型には、本発明の塗型材としてクロマイト粉末
g、s部に対しスラグ(第り表の屋/スラグ)/、0部
と有機粘結剤+有機相合剤(7,,5一部を混合しくク
ロマイト粉末ニスラグ−g9.夕: lo、s ) 、
iた従来方法による塗型材として前記配合物中のスラグ
に代えてCaco 3を等量刑えて混合し、それぞれ1
.P:*によってbo B6に調整したものを使用した
。鋳造されたそれぞれのボール弁のフランジ(フランジ
厚さ、2部mi)の断面の顕微鏡組織(70%しゆう酸
電解エツチング)を第3図(イ)、(ロ)に示す。(イ
)は本発明塗型材を施した鋳型によるものであり、SC
8I3の正常な組織となっている。これに対し、(ロ)
は従来方法による塗型祠を施した鋳型によるものであっ
て、浸炭によりfA jJJ!、面が約O1タ龍オース
テナイト単相となっており(δ7エライトが消失)、が
っ浸硫による点状硫化物(黒色)も認められる。
Example 2 SC81.3 ball valves were cast using furan resin molds (zircon sand) with different coatings. For the furan resin mold, as a coating material of the present invention, chromite powder g, s part, slag (Table 1) / 0 parts and organic binder + organic compatibilizer (7, 5 parts) were added. Mix chromite powder Nislag-g9. evening: lo, s),
As a mold coating material according to the conventional method, an equal amount of Caco 3 was added and mixed in place of the slag in the above formulation, and 1
.. P: * was used which was adjusted to bo B6. The microscopic structure (electrolytically etched with 70% oxalic acid) of the cross section of each cast ball valve flange (flange thickness, 2 parts mi) is shown in FIGS. 3(a) and 3(b). (A) is made of a mold coated with the mold coating material of the present invention, and SC
It has become a normal tissue of 8I3. On the other hand, (b)
is made from a mold that has been coated using the conventional method, and fA jJJ! is made by carburizing. The surface is a single phase of approximately O1 taryu austenite (δ7 elite has disappeared), and dotted sulfides (black) due to sulfurization are also observed.

前記実施例で示した従来方法による塗型材との比較から
明らかなように、本発明の塗型材は従来方法による塗型
材よシも浸炭・浸硫の防止効果において擾れていること
がわかる。
As is clear from the comparison with the mold coating material made by the conventional method shown in the above examples, it can be seen that the mold coating material of the present invention is less effective in preventing carburization and sulfurization than the mold coating material made by the conventional method.

本発明による効果を要約すると次のとおりである。The effects of the present invention are summarized as follows.

(1)  フラン樹脂鋳型による塗型材として本発明塗
型材を用いることによシ従来方法による塗型材に比べて
浸炭・浸硫をより効果的に防止し、まだ良好な鋳肌外観
が得られる。
(1) By using the mold coating material of the present invention as a mold coating material for furan resin molds, carburization and sulfurization can be more effectively prevented than in conventional mold coating materials, and a good casting surface appearance can still be obtained.

(2)  フラン樹脂鋳型による浸炭・浸硫に起因する
鋳造欠陥の発生がなくなる。
(2) Casting defects caused by carburizing and sulfurizing with furan resin molds are eliminated.

(3)  PJj造品鋳肌に浸炭・浸硫層がなくなるた
め鋳造品品質が向上する。
(3) Since there is no carburized or sulfurized layer on the casting surface of PJJ products, the quality of the cast products improves.

(4)  fQj造品鋳肌の浸炭・浸硫層の除去が不要
となシ、加工工数が減少し歩留族が向上する。
(4) There is no need to remove carburized and sulfurized layers on the casting surface of fQj products, reducing machining man-hours and improving yield.

(5)本発明で使用するスラグは製鋼工程で発生する産
業廃棄物であるためその有効利用が可能となる。
(5) Since the slag used in the present invention is industrial waste generated in the steel manufacturing process, it can be used effectively.

なお本発明塗型材は、合金鋳造品の浸炭・浸硫の防止を
目的としたものであるが、フラン樹脂鋳型への鋳込温度
が合金鋳造品に近い鋳鋼一般あるいは鋳鉄に対しても有
効であることはいうまでもない。
The mold coating material of the present invention is intended to prevent carburization and sulfurization of alloy castings, but it is also effective for cast steel in general or cast iron, where the casting temperature in furan resin molds is close to that of alloy castings. It goes without saying that there is.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、フラン樹脂鋳型に、本発明塗型材のスラグ含
有旭として不充分な量(3%)のスラグA/を添加した
塗型材を施しSC81,yを鋳造したときの鋳肌断面の
顕微鏡写真(エツチングせず)でちり、第、2図(イ)
、(ロ)は、SUS 、?コワJ/相当のステンレス鋼
鋳造品をフラン樹脂鋳型により製造したときの鋳肌各部
断l′I′iIの顕微鏡組織を示す写真であシ、(イ)
は本発明塗型材を施した部分における鋳肌断面の組織で
あり、(ロ)は従来方法による塗型材を施した部分にお
ける鋳肌断面の組織である。第3図(イ)、(ロ)は、
それぞれ異なる塗型を施したフラン樹脂鋳型によって5
C8I30ボール弁をそれぞれ鋳造したときの7ランジ
断面の顕微鏡に1目°とを示ず写真であシ、(イ)は本
発明塗層材を施・し水切型の場合であり、(ロ)は従来
方法による塗型材を施した鋳型の場合である。 特許出願人 日本冶金工業株式会社 代理人弁理士 村  1)  政  治第1図 第2図 (イ)
Figure 1 shows the cross-section of the casting surface when SC81,y was casted by adding an insufficient amount (3%) of slag A/ to the furan resin mold. Micrograph (not etched) showing dust, Figure 2 (A)
, (b) is SUS,? Photographs showing the microscopic structure of each section of the casting surface l'I'iI when a stainless steel casting equivalent to Kowa J was manufactured using a furan resin mold. (A)
(b) is the structure of the cross section of the casting surface in the part to which the mold coating material of the present invention was applied, and (b) is the structure of the casting surface cross section in the part to which the mold coating material according to the conventional method was applied. Figure 3 (a) and (b) are
5 by furan resin molds with different coatings.
The photographs show the 7-flange cross-section of each cast C8I30 ball valve (not shown). This is the case of a mold coated with a conventional method. Patent applicant Nippon Yakin Kogyo Co., Ltd. Representative Patent Attorney Mura 1) Politics Figure 1 Figure 2 (a)

Claims (1)

【特許請求の範囲】[Claims] 1、合金鋳造品製造の際に用いられるフラン樹脂鋳型用
塗型材において、塗型材中の骨材の構成成分として製鋼
工程の還元期に生成するスラグを全骨材中に5−xi−
o%金含有せてなることを特徴とするフラン樹脂鋳型用
塗型材。
1. In the coating material for furan resin molds used in the production of alloy casting products, 5-xi-
A coating material for furan resin molds, characterized by containing o% gold.
JP409283A 1983-01-17 1983-01-17 Mold coating material for furan resin casting mold Granted JPS59130644A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP409283A JPS59130644A (en) 1983-01-17 1983-01-17 Mold coating material for furan resin casting mold

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP409283A JPS59130644A (en) 1983-01-17 1983-01-17 Mold coating material for furan resin casting mold

Publications (2)

Publication Number Publication Date
JPS59130644A true JPS59130644A (en) 1984-07-27
JPS6125453B2 JPS6125453B2 (en) 1986-06-16

Family

ID=11575149

Family Applications (1)

Application Number Title Priority Date Filing Date
JP409283A Granted JPS59130644A (en) 1983-01-17 1983-01-17 Mold coating material for furan resin casting mold

Country Status (1)

Country Link
JP (1) JPS59130644A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103056288A (en) * 2013-01-25 2013-04-24 马鞍山市华达冶金机械有限公司 Lost foam casting paint for chromium-containing cast iron and preparation method thereof
CN103331410A (en) * 2013-01-29 2013-10-02 南京市溧水中山铸造有限公司 Novel coating material with high suspension and low concentration, coating method thereof and applications thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103056288A (en) * 2013-01-25 2013-04-24 马鞍山市华达冶金机械有限公司 Lost foam casting paint for chromium-containing cast iron and preparation method thereof
CN103056288B (en) * 2013-01-25 2014-12-03 马鞍山市华达冶金机械有限公司 Lost foam casting paint for chromium-containing cast iron and preparation method thereof
CN103331410A (en) * 2013-01-29 2013-10-02 南京市溧水中山铸造有限公司 Novel coating material with high suspension and low concentration, coating method thereof and applications thereof

Also Published As

Publication number Publication date
JPS6125453B2 (en) 1986-06-16

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