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JPS6234451B2 - - Google Patents
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JPS6234451B2 - - Google Patents

Info

Publication number
JPS6234451B2
JPS6234451B2 JP23063284A JP23063284A JPS6234451B2 JP S6234451 B2 JPS6234451 B2 JP S6234451B2 JP 23063284 A JP23063284 A JP 23063284A JP 23063284 A JP23063284 A JP 23063284A JP S6234451 B2 JPS6234451 B2 JP S6234451B2
Authority
JP
Japan
Prior art keywords
core
mold
casting
coating agent
coating layer
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
Application number
JP23063284A
Other languages
Japanese (ja)
Other versions
JPS61108446A (en
Inventor
Takeshi Imura
Shigemitsu Nakabayashi
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.)
Honda Motor Co Ltd
Original Assignee
Honda Motor 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 Honda Motor Co Ltd filed Critical Honda Motor Co Ltd
Priority to JP23063284A priority Critical patent/JPS61108446A/en
Publication of JPS61108446A publication Critical patent/JPS61108446A/en
Publication of JPS6234451B2 publication Critical patent/JPS6234451B2/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

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Mold Materials And Core Materials (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は例えば比較的低圧にて鋳造を行う金型
内にセツトする中子表面に塗布する塗型剤に関す
る。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a mold coating agent applied to the surface of a core set in a mold for casting, for example, at relatively low pressure.

(従来の技術) 自動車用シリンダブロツク、シリンダヘツド或
いはインテークマニホルド等は複雑形状をしてい
るため、これらを鋳造する場合には、金型内にシ
エルモールド、コールドボツクス等の砂中子をセ
ツトして鋳造し、鋳造後に中子を崩壊して複雑形
状の製品を得るようにしている。そして、中子を
用いて鋳造する場合には、溶湯圧力にて中子が圧
潰するおそれがあるため一般的には比較的低圧に
て鋳造を行うようにしている。
(Prior art) Since cylinder blocks, cylinder heads, intake manifolds, etc. for automobiles have complex shapes, when casting these, a sand core such as a shell mold or cold box is set in a mold. After casting, the core is collapsed to obtain products with complex shapes. When casting using a core, there is a risk that the core may be crushed by the pressure of the molten metal, so casting is generally performed at a relatively low pressure.

ところで、中子はケイ砂をバインダーにて固め
たものであるため、金型表面に比較しその表面は
粗く、そのままセツトしたのでは製品の鋳肌が荒
れたものとなる。そこで、従来から耐火物粉末等
を有機バインダーに溶解してなる塗型剤を中子表
面に塗布・乾燥せしめて被膜を形成した後に、金
型内にセツトするようにしている。
By the way, since the core is made of silica sand hardened with a binder, its surface is rougher than the surface of the mold, and if it is set as is, the casting surface of the product will be rough. Therefore, conventionally, a mold coating agent made by dissolving refractory powder or the like in an organic binder is applied to the surface of the core and dried to form a film, and then the core is set in a mold.

(発明が解決しようとする問題点) しかしながら、従来の塗型剤によつて形成され
る被膜は、鋳造時に溶湯の熱によつてバインダー
を構成するレジンが気化してガスを発生し、これ
が鋳巣などの鋳造欠陥の原因となり、また溶湯の
差し込みを十分に防止することができず、中子表
面に対する付着力も弱く、更には製品表面への焼
付き等の問題もある。
(Problems to be Solved by the Invention) However, in the case of coatings formed using conventional mold coating agents, the resin constituting the binder evaporates due to the heat of the molten metal during casting and generates gas. This causes casting defects such as cavities, cannot sufficiently prevent the insertion of molten metal, has weak adhesion to the surface of the core, and has problems such as seizure to the surface of the product.

(問題点を解決するための手段) 上記問題点を解決すべく本発明に係る中子用塗
型剤は、界面活性剤を添加した合成雲母水溶液に
天然の金雲母等の鱗片状耐火物粉末を混合して、
粘度が150〜300cpとなるようにした。
(Means for Solving the Problems) In order to solve the above problems, the core coating agent according to the present invention consists of a synthetic mica aqueous solution containing a surfactant and a scale-like refractory powder such as natural phlogopite. Mix the
The viscosity was set to 150 to 300 cp.

(実施例) 以下に本発明の実施例を添付図面を参照して説
明する。
(Example) Examples of the present invention will be described below with reference to the accompanying drawings.

先ず本発明に係る塗型剤を塗布する中子の造型
方法を述べる。
First, a method for molding a core by applying a mold coating agent according to the present invention will be described.

中子を造型するには、ケイ砂、ジルコンサン
ド、クロマイトサンド、或いはハイアルミナサン
ド等を骨材とし、これら骨材にフエノール樹脂等
の有機バインダーを混合して、型内に入れて焼成
する。このようにして抗析力35Kg/cm2乃至60Kg/
cm2の砂中子を得る。
To mold the core, silica sand, zircon sand, chromite sand, high alumina sand, or the like is used as aggregate, and an organic binder such as phenolic resin is mixed with the aggregate, and the mixture is placed in a mold and fired. In this way, the resistance force is 35Kg/cm 2 to 60Kg/
Obtain a sand core of cm 2 .

次いで、上記中子の表面に本発明に係る塗型剤
を塗布し、乾燥してコーテイング層を形成し中子
表面を平滑面とする。
Next, a mold coating agent according to the present invention is applied to the surface of the core and dried to form a coating layer to make the core surface smooth.

上記塗型剤を得るには、界面活性剤を添加した
合成雲母(ナトリウム・フツ素・4ケイ素又はリ
チウム・フツ素・4ケイ素を含む)水溶液に鱗片
状耐火物を混合してスラリーとすることで得る。
To obtain the above-mentioned mold coating agent, a scaly refractory is mixed into a synthetic mica (containing sodium, fluorine, 4-silicon or lithium, fluorine, 4-silicon) aqueous solution to which a surfactant has been added to form a slurry. Get it.

ここで前記鱗片状耐火物としては金属溶湯との
親和力が弱く、離型性に優れたものが好ましく、
例えば、金雲母(KMg3(Si3Al)O10(OH)2)、
絹雲母(セリサイト)又は鱗片状黒鉛等が挙げら
れる。
Here, the scale-like refractory is preferably one that has a weak affinity with molten metal and has excellent mold releasability,
For example, phlogopite (KMg 3 (Si 3 Al) O 10 (OH) 2 ),
Examples include sericite and flaky graphite.

そして、上記の如くスラリー状の塗型剤を中子
表面に塗布し、これを100℃以上で乾燥せしめて
コーテイング層を形成するわけであるが、このコ
ーテイング層の厚さは0.05〜0.2mmとすることが
好ましい、即ち、コーテイング層の厚さを0.05mm
未満とすると十分な耐圧性を発揮できず、コーテ
イング層の厚さを0.2mmより厚くすると鋳造後の
製品精度を維持できなくなる。そして、上記範囲
の厚さのコーテイング層を得るにはスラリー状の
塗型剤の粘度を150〜300cp(センチポイズ)と
する必要がある。また、第1図は、上記スラリー
粘度と、合成雲母及び鱗片状耐火物の溶媒(水)
に対する配合割合との関係を示すものであり、こ
の図から明らかな如く、スラリー状塗型剤の粘度
を150〜300cpとするには、合成雲母と鱗片状耐
火物を合計した重量比が溶媒に対して70〜150%
であることが条件となる。
Then, as described above, a slurry type coating agent is applied to the core surface and dried at 100°C or higher to form a coating layer, and the thickness of this coating layer is 0.05 to 0.2 mm. It is preferable to reduce the thickness of the coating layer to 0.05mm.
If it is less than 0.2 mm, sufficient pressure resistance cannot be exhibited, and if the thickness of the coating layer is thicker than 0.2 mm, the product precision after casting cannot be maintained. In order to obtain a coating layer having a thickness within the above range, the viscosity of the slurry coating agent must be 150 to 300 cp (centipoise). Figure 1 also shows the viscosity of the slurry and the solvent (water) for synthetic mica and flaky refractory.
As is clear from this figure, in order to set the viscosity of the slurry coating agent to 150 to 300 cp, the total weight ratio of synthetic mica and scale-like refractory to the solvent must be 70-150% against
The condition is that

第2図はコーテイング層を形成する前の中子表
面の粒子構造を示す250倍の顕微鏡写真であり、
第3図はコーテイング層を形成した後の中子表面
の粒子構造を示す250倍の顕微鏡写真である。こ
れらの図から明らかな如く、コーテイング層を形
成する以前にあつては中子表面は大きな空孔を有
しているが、コーテイング層を形成した後は、合
成雲母と鱗片状耐火物とが中子表面に層状をなし
て付着し、砂中子間の空孔を完全に覆い平滑な面
となつている。
Figure 2 is a 250x micrograph showing the particle structure of the core surface before forming the coating layer.
Figure 3 is a 250x micrograph showing the grain structure of the core surface after the coating layer has been formed. As is clear from these figures, the core surface has large pores before the coating layer is formed, but after the coating layer is formed, the synthetic mica and the scaly refractory are It adheres to the surface of the sand core in a layered manner, completely covering the pores between the sand cores and creating a smooth surface.

したがつて中子表面に溶湯の差し込みがない。
また、スラリー状塗型剤を構成する合成雲母は水
と接触して流動性を示し、この水溶性は付着力に
優れるため、コーテイング層は中子表面に強固に
付着する。一方、金雲母等の鱗片耐火物は金属溶
湯との親和力が弱いため、優れた離型性を示し、
また離型後の製品表面を付着したコーテイング層
は水と接触して流動性を示すので容易に除去する
ことができ、したがつて中子形状に制約が課せら
れない。
Therefore, there is no penetration of molten metal into the core surface.
Furthermore, the synthetic mica that constitutes the slurry coating exhibits fluidity when it comes into contact with water, and this water solubility provides excellent adhesion, so that the coating layer firmly adheres to the core surface. On the other hand, scale refractories such as phlogopite have a weak affinity with molten metal, so they exhibit excellent mold releasability.
Furthermore, the coating layer adhering to the product surface after release from the mold exhibits fluidity when in contact with water, so it can be easily removed, and therefore no restrictions are imposed on the core shape.

次に具体的な実験例を挙げ本発明の効果を更に
明確にする。ここで実験例1は自動車用シリンダ
ヘツドの鋳造用中子、実験例2は自動車用インテ
ークマニホールドの鋳造用中子についてのもので
ある。
Next, specific experimental examples will be given to further clarify the effects of the present invention. Here, Experimental Example 1 concerns a casting core for a cylinder head for an automobile, and Experimental Example 2 concerns a casting core for an automobile intake manifold.

実験例 1 骨材としてJIS7号ケイ砂(AFS110)100部、
有機バインダーとしてフエノールレジン3部、湿
潤剤としてステアリン酸カルシウム0.1部の配合
からなるシエル砂を用いて重量1.4Kgのウオータ
ージヤケツト中子を造型した。造型条件は金型温
度300℃、焼成時間40秒、吹込圧力2.5Kg/cm2であ
る。次にあらかじめ合成雲母(ナトリウム・フツ
素・4ケイ素を含む)の15%水溶液を十分に混合
撹拌したものを9.8Kg用意し、これに水10、湿
潤剤としてジアルキルスルホンコハク酸ナトリウ
ムの5%水溶液0.4Kg、平均粒子3μの金雲母
(KMg3(Si3Al)O10(OH)2)12Kg、及び消泡剤
0.02Kgを入れ1昼夜混合撹拌し、粘度150cpのス
ラリー状塗型剤を調整し、この塗型剤中に前記中
子を1〜2秒間浸漬し、大気中で60秒間放置後、
再度同じ溶液に1〜2秒間浸漬し、その後該中子
を170℃の乾燥にて20分間放置しコーテイング層
を形成した。
Experimental example 1 100 parts of JIS No. 7 silica sand (AFS110) as aggregate,
A water jacket core weighing 1.4 kg was molded using shell sand containing 3 parts of phenol resin as an organic binder and 0.1 part of calcium stearate as a wetting agent. The molding conditions were a mold temperature of 300°C, a firing time of 40 seconds, and a blowing pressure of 2.5 kg/cm 2 . Next, prepare 9.8 kg of a 15% aqueous solution of synthetic mica (containing sodium, fluorine, and 4 silicones) thoroughly mixed and stirred, add 10 kg of water, and 5% aqueous solution of sodium dialkyl sulfone succinate as a wetting agent. 0.4Kg, 12Kg of phlogopite (KMg 3 (Si 3 Al) O 10 (OH) 2 ) with an average particle size of 3μ, and antifoaming agent
0.02Kg was mixed and stirred for a day and night to prepare a slurry-like coating agent with a viscosity of 150 cp, the core was immersed in this coating agent for 1 to 2 seconds, and after being left in the air for 60 seconds,
The core was immersed again in the same solution for 1 to 2 seconds, and then the core was left to dry at 170° C. for 20 minutes to form a coating layer.

以上の如くして得られた中子を金型にセツト
し、アルミ合金(AC4B)を鋳造圧力0.3Kg/cm2
注湯温度700℃の条件下で低圧鋳造(LPDC)し
た。
The core obtained as above was set in a mold, and aluminum alloy (AC4B) was cast at a pressure of 0.3 kg/cm 2 .
Low-pressure casting (LPDC) was performed at a pouring temperature of 700℃.

鋳造後湯口切断を行い、JIS規格のTe(500℃
×4時間水冷、200℃×6時間空冷)処理を行つ
た後、通常のコアーノツクアクトマシンで中子の
砂落しを行つた。
After casting, the sprue is cut and the JIS standard Te (500℃
After treatment (water cooling for 4 hours, air cooling at 200°C for 6 hours), sand was removed from the core using a normal core knock act machine.

この結果中子折れ、変形は皆無で、且つ中子砂
は100%落ちていた。
As a result, there was no breakage or deformation of the core, and 100% of the core sand had fallen off.

更にその後、水圧2Kg/m2の水道水で洗浄した
ところ平滑で寸法精度の優れた製品を得た。
Furthermore, after washing with tap water at a water pressure of 2 kg/m 2 , a smooth product with excellent dimensional accuracy was obtained.

第4図Aは上記実験例1によつて得られた鋳造
品の表面粗さを測定した結果を示し、第4図Bは
従来方法によつて得られた鋳造品の表面粗さを測
定した結果を示すものであり、これらの図から明
らかな如く本発明はに係る塗型剤を塗布した中子
によつて形成された面粗度は15S前後となつてお
り、従来が40S前後であつたのに比べ大幅に向上
していることが分る。
Fig. 4A shows the results of measuring the surface roughness of the cast product obtained by the above Experimental Example 1, and Fig. 4B shows the result of measuring the surface roughness of the cast product obtained by the conventional method. As is clear from these figures, the surface roughness formed by the core coated with the coating agent of the present invention is around 15S, compared to the conventional one of around 40S. It can be seen that this is a significant improvement compared to the previous one.

実験例 2 実験例1と同様の配合及び造型条件からなるシ
エル砂を用いて重量3.2Kgのインテークマニホル
ド鋳造用中子を造型した。
Experimental Example 2 Shell sand having the same formulation and molding conditions as in Experimental Example 1 was used to mold an intake manifold casting core weighing 3.2 kg.

次にあらかじめ、合成雲母(ナトリウム・フツ
素・4ケイ素を含む)の15%水溶液を十分に混合
撹拌したものを20Kg用意し、これに水10、鱗片
状Al金属粉を25Kg配合し、更に湿潤剤としジア
ルキルスルホンコハク酸ナトリウムの5%水溶
液、0.8Kg、消泡剤0.1Kgを入れ1昼夜混合撹拌し
て粘度200cpのスラリー状塗型剤を調整した。こ
の塗型剤中に前記中子を前記実施例1と同様の条
件で浸漬し、コーテイング層を形成した。
Next, prepare 20 kg of a 15% aqueous solution of synthetic mica (including sodium, fluorine, and 4 silicones) thoroughly mixed and stirred, add 10 kg of water and 25 kg of scaly Al metal powder, and further moisten. A 5% aqueous solution of sodium dialkyl sulfone succinate (0.8 kg) and an antifoaming agent (0.1 kg) were added thereto and mixed and stirred for one day to prepare a slurry-like coating agent with a viscosity of 200 cp. The core was immersed in this mold coating agent under the same conditions as in Example 1 to form a coating layer.

以上の如くして得られた中子を金型にセツト
し、アルミ合金(AC2B)を鋳造圧力0.2Kg/cm2
注湯温度700℃の条件下で低圧鋳造(LPDC)し
た。
The core obtained as above was set in a mold, and aluminum alloy (AC2B) was cast at a pressure of 0.2 kg/cm 2 .
Low-pressure casting (LPDC) was performed at a pouring temperature of 700℃.

鋳造後湯口切断を行い、JIS規格のT6(500℃
×4時間水冷、170℃×4時間空冷)処理を行つ
た後、通常のコアーノツクアクトマシンで中子の
砂落としを行つた。
After casting, the sprue is cut to meet JIS standard T 6 (500℃
After treatment (water cooling x 4 hours, air cooling at 170°C x 4 hours), sand was removed from the core using a normal core knock act machine.

第5図A及びBに本発明による鋳物製品の中子
部表面粗さの測定結果と従来品の測定結果を示
す。これらの図より本発明のコーテイングによ
り、表面粗度は従来が54S前後のものが、10〜
15Sと大幅に向上しており、本発明の効果が大き
いことを表わしている。
FIGS. 5A and 5B show the measurement results of the surface roughness of the core part of the casting product according to the present invention and the measurement results of the conventional product. These figures show that with the coating of the present invention, the surface roughness has decreased from 54S to 10~10.
This is a significant improvement of 15S, indicating that the present invention is highly effective.

尚、前記金雲母、アルミ金属粉の代りに、絹雲
母、鱗状黒鉛を入れたものでも、同じく良好な結
果を得られた、更に本発明に係る塗型剤は低圧鋳
造用の中子に限らず、一般的な砂型鋳造、重力鋳
造の中子にも適用し得る。
In addition, similar good results were obtained even when sericite and scaly graphite were added instead of the phlogopite and aluminum metal powder.Furthermore, the mold coating agent according to the present invention is applicable only to cores for low-pressure casting. It can also be applied to cores for general sand casting and gravity casting.

(発明の効果) 以上の説明で明らかなように、本発明に係る塗
型剤を用いて鋳造用中子表面にコーテイング層を
形成すれば、中子表面の空孔を層状に完全に覆う
ことができるので、中子表面が平滑となり溶湯の
差し込みを防ぐことができる。また本発明に係る
塗型剤中には合成雲母が含まれているため、中子
表面に対する付着力が優れ、一方、溶湯との親和
力が弱い鱗片状耐火物が塗型剤中に含まれている
ため離型性に優れ、更にコーテイング層には有機
バインダーが含まれていないため、溶湯の熱によ
つてガスを発生することなく、鋳巣等の鋳造欠陥
のない製品を得ることができる。
(Effects of the Invention) As is clear from the above explanation, if a coating layer is formed on the surface of a casting core using the mold coating agent according to the present invention, the pores on the surface of the core can be completely covered in a layered manner. This makes the surface of the core smooth and prevents molten metal from penetrating. Furthermore, since the mold coating agent according to the present invention contains synthetic mica, it has excellent adhesion to the core surface, but on the other hand, the mold coating agent contains scale-like refractories that have a weak affinity with molten metal. Since the coating layer does not contain an organic binder, it does not generate gas due to the heat of the molten metal, and it is possible to obtain a product without casting defects such as blowholes.

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

第1図は、合成雲母及び鱗片状耐火物の配合割
合と塗型剤の粘度との関係を示すグラフ、第2図
はコーテイング層を形成する前の中子表面の粒子
構造を示す顕微鏡写真、第3図はコーテイング層
を形成した後の中子表面の粒子構造を示す顕微鏡
写真、第4図Aは実験例1によつて得られた鋳造
品表面の面粗度を示すグラフ、第4図Bは従来方
法によつて得られた鋳造品表面の面粗度を示すグ
ラフ、第5図Aは実験例2によつて得られた鋳造
品表面の面粗度を示すグラフ、第5図Bは従来方
法によつて得られた鋳造品表面の面粗度を示すグ
ラフである。
Fig. 1 is a graph showing the relationship between the blending ratio of synthetic mica and scaly refractory and the viscosity of the coating agent, Fig. 2 is a micrograph showing the particle structure of the core surface before forming the coating layer; Fig. 3 is a micrograph showing the particle structure of the core surface after the coating layer has been formed, Fig. 4A is a graph showing the surface roughness of the surface of the cast product obtained in Experimental Example 1, Fig. 4 B is a graph showing the surface roughness of the casting product surface obtained by the conventional method, FIG. 5A is a graph showing the surface roughness of the casting product surface obtained by Experimental Example 2, and FIG. 5B is a graph showing the surface roughness of a cast product surface obtained by a conventional method.

Claims (1)

【特許請求の範囲】 1 金属内にセツトされる砂中子表面に塗布され
る塗型剤において、この塗型剤は界面活性剤を添
加した合成雲母水溶液に鱗片状耐火物粉末を混合
したスラリー状をなし、且つこのスラリーの粘度
は150〜300cpとしたことを特徴とする中子用塗
型剤。 2 前記鱗片状耐火物粉末は天然の金雲母
(KMg3(Si3Al)010(OH)2)などの天然雲母であ
ることを特徴とする特許請求の範囲第1項記載の
中子用塗型剤。
[Claims] 1. A mold coating agent applied to the surface of a sand core set in a metal, which is a slurry of a synthetic mica aqueous solution containing a surfactant and a scale-like refractory powder mixed therein. A coating agent for a core, characterized in that the slurry has a viscosity of 150 to 300 cp. 2. The core according to claim 1, wherein the scale-like refractory powder is natural mica such as natural phlogopite (KMg 3 (Si 3 Al) 0 10 (OH) 2 ). Coating agent.
JP23063284A 1984-11-01 1984-11-01 Coating agent for core Granted JPS61108446A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23063284A JPS61108446A (en) 1984-11-01 1984-11-01 Coating agent for core

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23063284A JPS61108446A (en) 1984-11-01 1984-11-01 Coating agent for core

Publications (2)

Publication Number Publication Date
JPS61108446A JPS61108446A (en) 1986-05-27
JPS6234451B2 true JPS6234451B2 (en) 1987-07-27

Family

ID=16910826

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23063284A Granted JPS61108446A (en) 1984-11-01 1984-11-01 Coating agent for core

Country Status (1)

Country Link
JP (1) JPS61108446A (en)

Also Published As

Publication number Publication date
JPS61108446A (en) 1986-05-27

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