JPS60238058A - Casting method and mold coating material used therein - Google Patents

Casting method and mold coating material used therein

Info

Publication number
JPS60238058A
JPS60238058A JP9268584A JP9268584A JPS60238058A JP S60238058 A JPS60238058 A JP S60238058A JP 9268584 A JP9268584 A JP 9268584A JP 9268584 A JP9268584 A JP 9268584A JP S60238058 A JPS60238058 A JP S60238058A
Authority
JP
Japan
Prior art keywords
mold
oxide
casting
carburizing
substances
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.)
Pending
Application number
JP9268584A
Other languages
Japanese (ja)
Inventor
Mitsuhiko So
宗 光彦
Shingo Ichiyanagi
一柳 信吾
Susumu Nakayama
進 中山
Hiroyuki Yasunaga
安永 博幸
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.)
Daido Steel Co Ltd
Okazaki Minerals and Refining Co Ltd
Original Assignee
Daido Steel Co Ltd
Okazaki Minerals and Refining 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 Daido Steel Co Ltd, Okazaki Minerals and Refining Co Ltd filed Critical Daido Steel Co Ltd
Priority to JP9268584A priority Critical patent/JPS60238058A/en
Publication of JPS60238058A publication Critical patent/JPS60238058A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/02Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by additives for special purposes, e.g. indicators, breakdown additives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
    • B22C1/20Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents
    • B22C1/22Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins
    • B22C1/2233Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • B22C1/224Furan polymers

Abstract

PURPOSE:To suppress effectively carburization and sulfurization by allowing oxides consisting of iron oxide and manganese oxide to exist in a casting mold. CONSTITUTION:The oxides consisting of the iron oxide and manganese oxide are allowed to exist in the casting mold in the stage of using the org. self-curable furan resin mold obtd. by using an org. binder of an acid curing type consisting of a furan resin and a sulfonic acid curing catalyst in executing casting. The carburization and sulfurization occuring in the carburizing material such as carbon and sulfurizing material such as sulfur generated in the stage of pouring a molten metal into the furan resin mold are thus suppressed and prevented.

Description

【発明の詳細な説明】 この発明は鋳造方法およびこれに使用する塗型に関する
ものであって、更に詳細には、フラン樹脂鋳型への溶湯
注入時に発生する炭素(C)等の浸炭性物質および硫黄
(S)等の浸硫性物質に起因する浸炭現象および浸硫現
象を、特定の酸化物を前記鋳型内に存在させることによ
って抑制防止し、該浸炭・浸硫現象により惹き起こされ
る種々の問題点を解決するようにした浸炭・浸硫防止方
法およびこれに有利に使用される塗型に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a casting method and a coating mold used therein, and more particularly, the present invention relates to a casting method and a coating mold used therein. The carburizing and sulfurizing phenomena caused by sulfurizing substances such as sulfur (S) can be suppressed and prevented by the presence of specific oxides in the mold, and the various carburizing and sulfurizing phenomena caused by the carburizing and sulfurizing phenomena can be suppressed and prevented. The present invention relates to a method for preventing carburization and sulfurization that solves the problems, and a coating mold that is advantageously used for this method.

各種溶融金属(溶湯)を砂型または金型からなる鋳型中
に鋳込むことにより、所望形状の鋳造品が製造されるこ
とはよく知られているところである。
2. Description of the Related Art It is well known that a cast product having a desired shape can be manufactured by pouring various molten metals into a sand mold or a metal mold.

また前記鋳型として用いられる砂型にも、生型や油砂型
その他シェル型等各種のものがあり、用途に応じて適宜
使い分けられている。そして最近では、造型作業および
砂再生を容易化する見地から、砂に特殊な粘結剤と硬化
剤とを加えてす;(温で自然硬化させる有機自硬性りh
型が広く使用されるに至っている。
Furthermore, there are various types of sand molds used as the molds, such as green molds, oil sand molds, shell molds, etc., and they are used appropriately depending on the purpose. Recently, special binders and hardeners have been added to sand to facilitate molding operations and sand recycling;
The mold has come into widespread use.

有機自硬性鋳型の中でも、殊に酸硬化型の有機質粘結剤
とスルホン酸系硬化触媒とを用いて鋳物砂を造型した鋳
型は、硬化が速やかに進行して高い型強度が得られ、し
かも鋳込時の高熱によりスルホン酸が分解・消失するの
で鋳物砂の再使用ができる等の利点がある。より具体的
にこの種の有機自硬性鋳型を例示すると、シリカサンド
、ジルコンサンド、クロマイトサンド等の鋳物砂に、フ
ラン樹脂、レゾール型フェノール樹脂、尿素樹脂、また
は尿素樹脂若しくはフェノール樹脂で変成したフラン樹
脂等の酸硬化型の有機質粘結剤と、パラ1へルエンスル
ホン酸、キシレンスルホン酸等のスルホン酸系硬化触媒
(硬化剤あるいは硬化促進剤)とを加えて混合した後、
該混合材料により造型を行い、次いて常温または比較的
に低い温度で加温硬化させることによって、所定のU型
を得るものである。
Among organic self-hardening molds, molds made from foundry sand using an acid-curing organic binder and a sulfonic acid-based curing catalyst have rapid hardening and high mold strength. Since the sulfonic acid decomposes and disappears due to the high heat during casting, there are advantages such as the ability to reuse the foundry sand. More specifically, examples of this type of organic self-hardening mold include foundry sand such as silica sand, zircon sand, chromite sand, etc., and furan resin, resol type phenolic resin, urea resin, or furan modified with urea resin or phenol resin. After adding and mixing an acid-curing type organic binder such as a resin and a sulfonic acid curing catalyst (curing agent or curing accelerator) such as para-1 toluenesulfonic acid or xylene sulfonic acid,
A predetermined U-shape is obtained by molding the mixed material and then heating and curing it at room temperature or a relatively low temperature.

ところで前述した各種の有機自硬性鋳型のうち、フラン
樹脂からなる有機質粘結剤およびスルホン酸系硬化触媒
を用いて造型したフラン樹脂鋳型を使用して鋳造を行な
うと、鋳造品の表層に炭素(C)および硫黄(S)が濃
化する現象が認められる。そしてこのような炭素および
硫黄の濃化により、鋳造品の熱間亀裂が助長されたり、
耐蝕性が低下したり、更にはその機械的性質が劣化する
等の問題点が種々惹起されることが知られている。
By the way, among the various organic self-hardening molds mentioned above, when casting is performed using a furan resin mold molded using an organic binder made of furan resin and a sulfonic acid curing catalyst, carbon ( A phenomenon in which C) and sulfur (S) are concentrated is observed. This enrichment of carbon and sulfur may promote hot cracking in castings,
It is known that various problems occur, such as a decrease in corrosion resistance and further deterioration of its mechanical properties.

そこで本願の発明台等はその問題点を解明するべく鋭意
検討を進めたところ、前記フラン樹脂新型に溶湯を鋳込
む際の高熱によって、該鋳型中に含まれるフラン樹脂の
有機質粘結剤が熱分解して炭素(C)やその化合物(浸
炭性物質)を生じ、これが溶湯内に浸入して殊に溶馬表
層部における炭素(C)を濃化させる浸炭現象を生起し
、前記不都合を惹起するに至ることを突止めた。すなわ
ち浸炭現象については、有機自硬性鋳型のなかではフラ
ン樹脂鋳型を用いた湯今に顕著に認められるとこ3− ろから、フラン樹脂の有機質粘結剤に含まれる炭素(C
)含有成分が熱分解してCα、CIT、、等を発生し、
これが鋳物表面の高温部で分解して炭素等の浸炭性物質
を生じて前記浸炭現象を惹起するものど行えられる。
Therefore, the inventors of the present application conducted intensive studies to solve this problem, and found that the organic binder of the furan resin contained in the mold was heated due to the high heat when pouring molten metal into the new type of furan resin. It decomposes to produce carbon (C) and its compounds (carburizable substances), which infiltrate into the molten metal and cause a carburizing phenomenon that concentrates carbon (C), especially in the surface layer of the molten metal, causing the above-mentioned disadvantages. I discovered what led to this. In other words, the carburization phenomenon is most noticeable among organic self-hardening molds in hot water molds using furan resin molds.
) The contained components thermally decompose to generate Cα, CIT, etc.
This can be done by decomposing at the high-temperature part of the surface of the casting, producing carburizing substances such as carbon, and causing the carburizing phenomenon described above.

また同じくフラン樹脂新型への注湯時に該鋳型に付すさ
れろ高熱によって、スルホン酸系硬化触媒が熱分解して
硫黄(S)やその化合物(浸硫性物質)を生じ、これが
溶湯内に浸入して溶?易表層部における硫黄(S)を濃
化させる浸硫現象を生起し、前記不都合を惹起すること
をO[せて知見した。すなわち浸硫現象に関しては、有
機自硬性鋳型のなかではスルホン酸系硬化触媒を用いた
場合にのみ認められ、かつフラン樹脂th型は前記スル
ホン酸系硬化触媒を使用するものであるところから、こ
のスルホン酸系の硬化触媒に含まIするスルホン酸基な
どの硫黄(S)含有成分が、高熱の溶湯注入により熱分
解してSO2等を発生し、更にそれらが鋳物表面の高温
部で分解して硫黄等の浸硫性物質を生じ、njl記tシ
硫rS1象を惹起するものと汚えられる。
Similarly, when pouring into a new type of furan resin, the high heat applied to the mold causes the sulfonic acid curing catalyst to thermally decompose, producing sulfur (S) and its compounds (sulfurizable substances), which infiltrate into the molten metal. And melt? It has been found that O[O] causes a sulfurization phenomenon that concentrates sulfur (S) in the surface layer, causing the above-mentioned disadvantages. In other words, the sulfurization phenomenon is observed among organic self-hardening molds only when a sulfonic acid-based curing catalyst is used, and since the furan resin th type uses the sulfonic acid-based curing catalyst, this Sulfur (S)-containing components such as sulfonic acid groups contained in sulfonic acid-based curing catalysts are thermally decomposed by injection of high-temperature molten metal and generate SO2, etc., which are further decomposed at the high temperature part of the casting surface. It produces sulfurizable substances such as sulfur and is contaminated with substances that cause the sulfur phenomenon.

−4= 本発明に係る鋳造品の浸炭・浸硫防止方法は、このよう
な知見に基づいて、その対策手段につき種々検討した結
果として完成されたものであって、その要旨とすること
ろは、溶湯鋳込時に浸炭性物質および浸硫性物質を発生
する材料を含む鋳型を用いて鋳造を行うに際し、前記鋳
型内にFe3O4等の酸化鉄およびM n 20 :l
やMnO2等の酸化マンガンの如き特定の酸化物を存在
せしめ、これにより前記浸炭性物質および浸硫性物質に
起因する浸炭現象および浸硫現象を抑制するようにした
ことを特徴どする。
-4= The method for preventing carburization and sulfurization of cast products according to the present invention was completed as a result of various studies on countermeasures based on such knowledge, and the gist of the method is as follows. When casting is performed using a mold containing a material that generates carburizing substances and sulfurizing substances when pouring molten metal, iron oxide such as Fe3O4 and M n 20 :l are contained in the mold.
The present invention is characterized in that a specific oxide such as manganese oxide such as MnO2 or MnO2 is present, thereby suppressing the carburizing phenomenon and sulfurizing phenomenon caused by the carburizing substance and sulfurizing substance.

また前記鋳造品の浸炭・浸硫防止方法を実施するに際し
ては、酸化鉄および酸化マンガンからなる酸化物を20
〜60%含有してなる塗型を好適に使用することができ
る。
In addition, when carrying out the method for preventing carburization and sulfurization of cast products, oxides consisting of iron oxide and manganese oxide are
A coating mold containing up to 60% can be suitably used.

このように本発明は、酸化鉄および酸化マンガンからな
る各酸化物を鋳型内に存在させることにより、前記浸炭
現象よ;よび浸硫現象を効果的に抑制しようとするもの
であるが、その浸炭才;よび浸硫防止の原理については
未だ明らかにはされていない。この浸炭および浸硫防止
機構について推定を進めれば、物理的方法と化学的方法
との2種類の存在が考えられる。すなわち物理的方法と
しては、酸化物の存在下に鋳型と溶湯との間に低溶融物
乃至焼結層を形成して、鋳込時に生ずる分解ガスを遮蔽
し、これにより浸炭・浸硫現象を防止し得るものと推定
される。また化学的方法としては、酸素(○)を放出し
、浸炭性ガスを酸化させることにより浸炭現象を緩和す
ることができると推定される。
As described above, the present invention attempts to effectively suppress the carburizing phenomenon and the sulfurizing phenomenon by making each oxide consisting of iron oxide and manganese oxide exist in the mold. The principle of preventing oxidation and sulfurization has not yet been clarified. When estimating this carburization and sulfurization prevention mechanism, two types of methods can be considered: a physical method and a chemical method. In other words, as a physical method, a low melting material or sintered layer is formed between the mold and the molten metal in the presence of oxides to block the decomposition gas generated during casting, thereby preventing carburizing and sulfurizing phenomena. It is presumed that this can be prevented. Furthermore, as a chemical method, it is presumed that the carburizing phenomenon can be alleviated by releasing oxygen (◯) and oxidizing the carburizing gas.

そして本発明に従えば、かかる炭素(C)等の浸炭性物
質および硫黄(S)等の浸硫性物質が、注湯、凝固、型
バランまでの過程で前記酸化鉄および酸化マンガン等の
特定の酸化物によって、非浸炭性の物質および非浸硫性
の物質とされたり、あるいはGD3やSO2などに転化
されたりして、εh梨型外放出される等の理由により、
鋳物表面の浸炭現象および浸硫現象が効果的に抑制され
るものと推定される。
According to the present invention, carburizable substances such as carbon (C) and sulfurizable substances such as sulfur (S) are used to identify iron oxides, manganese oxides, etc. during the process of pouring, solidifying, and mold balun. Due to reasons such as being converted into non-carburizing substances and non-sulfurizing substances by oxides of
It is presumed that carburizing and sulfurizing phenomena on the surface of the casting are effectively suppressed.

なお、本発明に従ってFeff04等の酸化鉄およびM
n2O3やMnO2等の酸化マンガンの如き特定の酸化
物を、鋳型内に存在せしめる手法としては種々の方法が
ある。例えば鋳型の造型時に鋳物砂中に前記Fe3O4
等の酸化物を混合せしめて使用することにより、該酸化
物を主型、中子などの内部に均一に分散せしめたり、ま
たそれらの内部に(表層部近傍に)層状に該酸化物量の
多い層を形成せしめたり、更には鋳型の表面に塗布せし
めたり、また鋳型を形成するフィルム、ブロックなどの
材料の表面に塗布せしめたりすること等によって行なわ
れる。なかでも、一般に鋳型の塗型に用いられ塗型剤中
に、Fe−04等の酸化鉄およびMn20aやMnO7
等の酸化マンガンの如き特定の酸化物を混入せしめるこ
とにより、鋳型表面に該特定の酸化物が存在せしめられ
るようにすることが望ましい。またこのようにして鋳型
内に存在せしめられる特定の酸化物の量は、それの鋳型
内の存在形態によって種々異なり、−・箆的に限定し得
るものではないが、一般に20重量%程度以」二の割合
にて塗型剤中に存在せしめることが好まし7− く、またその上限としては、塗型剤中に存在せしめると
きには約60重量%程度までとすることが好ましい。
In addition, according to the present invention, iron oxide such as Feff04 and M
There are various methods for making a specific oxide such as manganese oxide such as n2O3 or MnO2 exist in the mold. For example, when making a mold, the Fe3O4 is added to the foundry sand.
By mixing and using oxides such as oxides, it is possible to uniformly disperse the oxides inside the main mold, core, etc., or to form a layer inside them (near the surface layer) with a large amount of oxides. This can be done by forming a layer, or by coating the surface of a mold, or by coating the surface of a material such as a film or block that forms the mold. Among these, iron oxides such as Fe-04 and Mn20a and MnO7 are generally used in mold coatings.
It is desirable to make the specific oxide present on the surface of the mold by mixing a specific oxide such as manganese oxide. The amount of the specific oxide present in the mold in this way varies depending on the form in which it exists in the mold, and although it cannot be strictly limited, it is generally about 20% by weight or less. It is preferable that it be present in the mold coating agent in a ratio of 2 to 2, and the upper limit thereof is preferably about 60% by weight when it is present in the mold coating agent.

以下に本発明に係る浸炭・浸硫防止方法の好適な実施例
を示すが、本発明がこれら実施例の記載によって何等の
制限をも受けるものでないことは勿論である。なお実施
例中、百分率および部は特に断りのない限り、すべて重
量基準によるものである。
Preferred embodiments of the method for preventing carburization and sulfurization according to the present invention are shown below, but it goes without saying that the present invention is not limited in any way by the description of these embodiments. In the examples, all percentages and parts are based on weight unless otherwise specified.

実施例 第1(a)〜(c)図に示す形状の中空バルブ鋳造品を
鋳込めるように、シリカサンドからなる鋳物砂98.4
部と、酸硬化型の有機質粘結剤としてのフラン樹脂1.
0部と、硬化触媒としてのパラトルエンスルホン酸0.
6部とを混合せしめたものを材料として、所定のフラン
樹脂鋳型を造型し、当該鋳型内面には、本発明に従う下
記の塗型剤を塗布した。この塗型剤には、Fes○4の
酸化鉄およびM n 20 sの酸化マンガンを配合比
67:33(約2:1)で配合してなる酸化物を、骨材
として208− 〜60%含有させた。塗布方法は、二層の重ね塗りとし
、下塗り塗型として前記塗型剤を塗布し、上塗り塗型に
は溶湯との耐焼着性を持たせるためにジルコン系アルコ
ール性塗型剤(例えば岡崎鉱産物(株)製の商品名才力
スーパー800)を使用した。
Example 1 Foundry sand 98.4 made of silica sand was used to cast a hollow valve casting product having the shape shown in FIGS. 1(a) to (c).
and furan resin as an acid-curable organic binder.
0 parts and 0.0 parts of para-toluenesulfonic acid as a curing catalyst.
A predetermined furan resin mold was made using a mixture of 6 parts and 6 parts, and the following mold coating agent according to the present invention was applied to the inner surface of the mold. This mold coating agent contains an oxide made by blending iron oxide of Fes○4 and manganese oxide of M n 20 s in a blending ratio of 67:33 (approximately 2:1), with an aggregate content of 208- to 60%. Contained. The coating method is two-layered coating, in which the above-mentioned coating agent is applied as the undercoat, and the topcoat is coated with a zircon-based alcohol-based coating agent (for example, Okazaki Mineral Co., Ltd.) to provide resistance to scorching with the molten metal. The product (trade name: Sairiki Super 800) manufactured by Mono Co., Ltd. was used.

下塗り塗型の濃度調整にはエタノールを使用し、塗型乾
燥はバーナーにて行った。なお鋳肌改善のために、ジル
コンフラワーを含有させた。但し、浸炭・浸硫防止の目
的のためだけであるならば、アルミナフラワー、シャモ
ットフラワー、ムライトフラワー、クロマイ1−フラワ
ー、シリカフラワーその他マグネシアフラワー等も好適
に使用される。
Ethanol was used to adjust the density of the undercoat mold, and the paint mold was dried using a burner. In order to improve the casting surface, zircon flour was added. However, if it is only for the purpose of preventing carburization and sulfurization, alumina flour, chamotte flour, mullite flour, chromium 1-flower, silica flour, magnesia flour, etc. are also suitably used.

次いで前記鋳型内に溶湯をそれぞれ鋳込み、所望の鋳造
品を製造した。供試材、すなわち板状鋳造品の表面をサ
ンド・ブラスト処理してスケールを除いた後、該供試材
表層から第1(a)〜(c)図のA〜Eに示す各部分に
おいて、0〜0.5mm、0.5−1 、 Oiwnお
よび]、 、 O−1、5mnの3段階にてダライ粉を
採取し、炭素(C)および硫黄(S)分析に供した。こ
の分析の結果を、供試材に係る鋳造品表面からの距離と
炭素(C)および硫黄(S)含有量との関係として、第
2図に示した。但し第2図中において、No、1は比較
のため酸化物を含有しない塗型を示し、N002はFe
50.tの酸化鉄およびMn20+の酸化マンガンを配
合比約2:1で配合してなる酸化物を20%含有させた
塗型、No、3は前記酸化物を30%含有させた塗型、
No、4は酸化物を40%含有させた塗型、No、5は
酸化物を50%含有させた塗型を夫々示す。
Next, the molten metal was poured into each of the molds to produce a desired cast product. After removing scale by sand blasting the surface of the test material, that is, the plate-shaped cast product, in each part shown in A to E in FIGS. 1(a) to (c) from the surface layer of the test material, Dried powder was collected in three stages: 0 to 0.5 mm, 0.5-1 mm, Oiwn and ], O-1, and 5 mm, and subjected to carbon (C) and sulfur (S) analysis. The results of this analysis are shown in FIG. 2 as the relationship between the distance from the surface of the cast product and the carbon (C) and sulfur (S) contents of the sample material. However, in Fig. 2, No. 1 indicates a coating mold containing no oxide for comparison, and No. 1 indicates a coating mold containing no oxide.
50. No. 3 is a coating mold containing 20% of an oxide made by blending iron oxide of t and manganese oxide of Mn20+ at a blending ratio of about 2:1, No. 3 is a coating mold containing 30% of the oxide,
No. 4 indicates a coating mold containing 40% oxide, and No. 5 indicates a coating mold containing 50% oxide.

酸化物を含有させた塗型剤を塗布した鋳型を使用した場
合は、第2図のNo、2〜No、5に示す如く、供試材
に係る鋳造品表層の0%および8%と、鋳造品深部(中
心部側)の0%および8%との間には殆んど差が認めら
れない。これに対し、酸化物を含有しない塗型剤を使用
した鋳型にあっては、第2図のNo、1に示される如く
、鋳造品表層部の0%および8%が、深部の0%および
8%に対して極めて高い値を示した。こfitらの事実
より、従来のFe3O4の酸化鉄およびM n 203
の酸化マンガンを配合比約2:1で配合してなる酸化物
を存在せしめないフラン樹脂鋳型を用いて得られる鋳造
品に惹起される表層部の浸炭現象にょるC濃化および浸
硫現象によるS濃化の問題が、本発明に係る方法および
塗型によって効果的に解決され得ることは明白である。
When using a mold coated with a mold coating agent containing an oxide, as shown in Nos. 2 to 5 in Figure 2, 0% and 8% of the surface layer of the cast product related to the sample material, There is almost no difference between 0% and 8% in the deep part of the cast product (center side). On the other hand, in a mold using a coating agent that does not contain oxides, as shown in No. 1 in Figure 2, 0% and 8% of the surface layer of the cast product are 0% and 8% of the deep layer. It showed an extremely high value compared to 8%. From the facts of Kofit et al., conventional iron oxide of Fe3O4 and M n 203
Due to carbon concentration and sulfurization caused by the carburization phenomenon in the surface layer of a cast product obtained using an oxide-free furan resin mold containing manganese oxide in a blending ratio of about 2:1. It is clear that the problem of S enrichment can be effectively solved by the method and mold according to the invention.

なお本発明に係る浸炭・浸硫防止作用を為す特定の酸化
物として、M n 202の酸化マンガンに代えて、他
のM n O2の酸化マンガンなどを用いて上記実験を
繰り返したところ、程度の差はあるものの、同様な結果
を得られることが認められた。
In addition, when the above experiment was repeated using other manganese oxides such as M n O2 in place of M n 202 manganese oxide as the specific oxide that has the effect of preventing carburization and sulfurization according to the present invention, it was found that a certain degree of Although there were differences, it was observed that similar results could be obtained.

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

第1(a)〜(c)図は供試材に係る中空バルブ鋳造品
の各断面図、第2図は実施例においてめられた鋳造品表
面からの距離に対する炭素(C)および硫黄(S)含有
量の関係を示すグラフである。 特許出願人 大同特殊鋼株式会社 FI( (a) (C) (b)
Figures 1 (a) to (c) are cross-sectional views of hollow valve castings related to test materials, and Figure 2 shows carbon (C) and sulfur (S) ) is a graph showing the relationship between contents. Patent applicant: Daido Steel Co., Ltd. FI ((a) (C) (b)

Claims (6)

【特許請求の範囲】[Claims] (1)溶湯鋳込時に浸炭性物質および浸硫性物質を発生
する材料を含む鋳型を用いて鋳造を行うに際し、前記鋳
型内に酸化鉄および酸化マンガンの各酸化物を存在せし
め、これにより前記浸炭性物質および浸硫性物質に起因
する浸炭現象および浸硫現象を抑制するようにしたこと
を特徴とするMt造方法
(1) When performing casting using a mold containing a material that generates carburizing substances and sulfurizing substances when pouring molten metal, each oxide of iron oxide and manganese oxide is made to exist in the mold, thereby causing the A Mt manufacturing method characterized by suppressing carburizing and sulfurizing phenomena caused by carburizing substances and sulfurizing substances.
(2)前記鋳型は、フラン樹脂からなる酸硬化型の有機
質粘結剤とスルホン酸系硬化触媒とを用いて得られる有
機自硬性のフラン樹脂鋳型である特許請求の範囲第1項
記載の鋳造正方法。
(2) The casting according to claim 1, wherein the mold is an organic self-hardening furan resin mold obtained using an acid-curing organic binder made of a furan resin and a sulfonic acid curing catalyst. Correct method.
(3)前記酸化鉄は、Fe5r4である特許請求の範囲
第1項記載の鋳造方法。
(3) The casting method according to claim 1, wherein the iron oxide is Fe5r4.
(4)前記酸化マンガンは、Mn2O3またはMnO2
である特許請求の範囲第1項記載の鋳造方法。
(4) The manganese oxide is Mn2O3 or MnO2
A casting method according to claim 1.
(5)酸化鉄および酸化マンガンからなる酸化物を20
〜60%含有してなる塗型。
(5) Oxide consisting of iron oxide and manganese oxide
A coating mold containing ~60%.
(6)前記酸化物における酸化鉄と酸化マンガンどの配
合比は、約2:1である特許請求の範囲第5項記載の塗
型。
(6) The coating mold according to claim 5, wherein the mixing ratio of iron oxide and manganese oxide in the oxide is about 2:1.
JP9268584A 1984-05-09 1984-05-09 Casting method and mold coating material used therein Pending JPS60238058A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9268584A JPS60238058A (en) 1984-05-09 1984-05-09 Casting method and mold coating material used therein

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9268584A JPS60238058A (en) 1984-05-09 1984-05-09 Casting method and mold coating material used therein

Publications (1)

Publication Number Publication Date
JPS60238058A true JPS60238058A (en) 1985-11-26

Family

ID=14061342

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9268584A Pending JPS60238058A (en) 1984-05-09 1984-05-09 Casting method and mold coating material used therein

Country Status (1)

Country Link
JP (1) JPS60238058A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001269767A (en) * 2000-03-27 2001-10-02 Kurimoto Ltd Method for producing spheroical graphite cast iron product

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001269767A (en) * 2000-03-27 2001-10-02 Kurimoto Ltd Method for producing spheroical graphite cast iron product

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