JPS61199545A - Consumable pattern material for casting - Google Patents

Consumable pattern material for casting

Info

Publication number
JPS61199545A
JPS61199545A JP3987385A JP3987385A JPS61199545A JP S61199545 A JPS61199545 A JP S61199545A JP 3987385 A JP3987385 A JP 3987385A JP 3987385 A JP3987385 A JP 3987385A JP S61199545 A JPS61199545 A JP S61199545A
Authority
JP
Japan
Prior art keywords
casting
resin
weight
particles
parts
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
JP3987385A
Other languages
Japanese (ja)
Other versions
JPH0318532B2 (en
Inventor
Hideki Kuwabara
英樹 桑原
Masato Naito
真人 内藤
Teishiro Watanabe
渡辺 貞四郎
Tadatsugu Hamada
浜田 忠嗣
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.)
JSP Corp
Mitsubishi Heavy Industries Ltd
Original Assignee
JSP Corp
Mitsubishi Heavy Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by JSP Corp, Mitsubishi Heavy Industries Ltd filed Critical JSP Corp
Priority to JP3987385A priority Critical patent/JPS61199545A/en
Priority to DE8686301032T priority patent/DE3675042D1/en
Priority to EP86301032A priority patent/EP0195512B1/en
Priority to US06/830,730 priority patent/US4711287A/en
Priority to CA000502477A priority patent/CA1248322A/en
Publication of JPS61199545A publication Critical patent/JPS61199545A/en
Publication of JPH0318532B2 publication Critical patent/JPH0318532B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C9/00Moulds or cores; Moulding processes
    • B22C9/02Sand moulds or like moulds for shaped castings
    • B22C9/04Use of lost patterns
    • B22C9/046Use of patterns which are eliminated by the liquid metal in the mould

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Molds, Cores, And Manufacturing Methods Thereof (AREA)

Abstract

PURPOSE:To reduce the cost of a product by forming a pattern material of a crosslinked foamed-in-place molding of which the resin consists of a PP resin and high density polyethylene and which has specific density. CONSTITUTION:The pattern material is formed of the crosslinked foamed-in- place molding of which the resin consists of the PP resin and/or high density polyethylene and which has 0.025-0.012g/cm<2> density. The PP resin to be used for such full mold pattern material is exemplified by an ethylene/propylene random copolymer, ethylene/propylene block copolymer, propylene homopolymer, etc. Since the resin and the density are specified in the above-mentioned manner, the resin is easily gasified when the resin contacts with the molten metal poured into the mold. No soot is generated in such a stage. The resultant casting has no surface defects such as 'gas pockets' and 'wave-like surface folding' owing to the unevaporated residue and is free from the carburization in the casting. The casting has excellent dimensional accuracy as well.

Description

【発明の詳細な説明】 (技術分野〕 本発明は、注入された溶湯に置換されて鋳物を製作する
消失模型鋳造法において、合成樹脂発泡体の化学特性に
起因する鋳造欠陥の発生がなく、かつ消失し易い合成樹
脂発泡体からなる鋳造用消失模型材料に関する。   
゛ 〔従来技術〕 従来より合成樹脂発泡体を鋳造用消失模型に使用するこ
とはフルモールド法として公知である。
DETAILED DESCRIPTION OF THE INVENTION (Technical Field) The present invention provides a method for eliminating casting defects caused by the chemical properties of synthetic resin foam in a vanishing model casting method in which casting is produced by replacing the molten metal with injected metal. The present invention also relates to a disappearing model material for casting made of a synthetic resin foam that easily disappears.
[Prior Art] The use of synthetic resin foam as a vanishing model for casting has been known as the full mold method.

フルモールド法は、通常、ポリスチレンからなるプラス
チック発泡体にて模型を作成し、これを鋳型の中に埋め
、そのままの状態で溶湯を注入し。
In the full mold method, a model is usually made from a plastic foam made of polystyrene, which is then buried in a mold and molten metal is injected into the mold.

溶湯の熱によって前記プラスチック発泡体の模型をガス
化消失させると共に、その空洞部分に湯を充満させ、冷
却して鋳物を得る方法である。従って、このフルモール
ド法は、模型の製作から鋳型製作までの工程が著°シ<
簡素化された画期的な鋳造方法と言うことができる。
This is a method in which the plastic foam model is gasified and disappeared by the heat of the molten metal, and the cavity is filled with hot water and cooled to obtain a casting. Therefore, in this full mold method, the process from making the model to making the mold is extremely simple.
It can be said to be a simplified and innovative casting method.

しかしながら、鋳造用消失模型材料として従来から使用
されるポリスチレンは、熱分解しにくいという化学特性
を有することがら、これをフルモ−ルド用模型材料とし
て使用して得られた鋳物は、その表面に未気化残渣によ
る「ガスじわ」又は「波状あれ」等の表面欠陥や鋳物内
部における加炭現象1時には分解ガスの巻き込みによる
ガス欠陥を発生する問題があった。従って、従来の場合
は、この様な鋳物は、製品とするために、鋳物表面を機
械的に仕上げ処理するという余分な工程が必要であった
り、ガス欠陥のある製品の場合には廃棄を余儀なくされ
ていた。
However, polystyrene, which has traditionally been used as a disappearing model material for casting, has a chemical property that makes it difficult to thermally decompose. In case of surface defects such as "gas wrinkles" or "wavyness" due to vaporized residue, and carburization inside the casting, there were problems in which gas defects were generated due to entrainment of decomposed gas. Therefore, in the past, such castings required an extra step of mechanically finishing the surface of the casting to make them into products, or had to be discarded if they had gas defects. It had been.

〔目   的〕〔the purpose〕

本発明は、従来鋳造用消失模型材料に見られるこれらの
問題を解決し1合成樹脂発泡体の化学特性による鋳物欠
陥を生じず1表面仕上げ処理などの後処理工程を必要と
しない鋳物を与える合成樹脂発泡体からなる鋳造用消失
模型材料を提供することを目的とする。
The present invention solves these problems seen in conventional vanishing model materials for casting, and provides a synthetic resin that produces castings that do not cause casting defects due to the chemical properties of the synthetic resin foam and do not require post-processing steps such as surface finishing. The object of the present invention is to provide a disappearing model material for casting made of resin foam.

〔構  成〕 本発明は、構成する樹脂がポリプロピレン系樹脂及びl
又は高密度ポリエチレンからなり、密度が0.025〜
0.012g/clである架橋発泡型内成形体よすなる
ことを特徴とする鋳造用消失模型材料を要旨とする。
[Configuration] In the present invention, the constituting resin is a polypropylene resin and l
Or made of high density polyethylene, with a density of 0.025~
The gist of the present invention is a disappearing model material for casting, which is characterized by a cross-linked foamed in-mold molded product having a density of 0.012 g/cl.

本発明の鋳造用模型素材樹脂、即ち、フルモールド用模
型材料として用いるポリプロピレン系樹脂としては、エ
チレン−プロピレンランダム共重合体、エチレン−プロ
ピレンブロック共重合体、プロピレン雫独重合体、プロ
ピレン−1−ブテンランダム共重合体などが挙げられる
。特に、これらの重合体の中で、エチレン含有量1゜0
1量%〜10重量%で、かつn−へブタン抽出残渣割合
が50重量%以下のエチレン−プロピレンランダム共重
合体の使用が好ましい。この場合、n−ヘプタン抽出残
渣割合とは、立体規則性を意味し、次の式で表わされる
The casting model material resin of the present invention, that is, the polypropylene resin used as the full mold model material, includes ethylene-propylene random copolymer, ethylene-propylene block copolymer, propylene droplet monopolymer, propylene-1- Examples include butene random copolymers. In particular, among these polymers, ethylene content of 1°0
It is preferable to use an ethylene-propylene random copolymer having a content of 1% by weight to 10% by weight and a proportion of n-hebutane extraction residue of 50% by weight or less. In this case, the n-heptane extraction residue ratio means stereoregularity and is expressed by the following formula.

R(%)=−xto。R (%) = -xto.

R:n−ヘプタン抽出残渣割合 A:n−へブタン8時間抽出後の不溶分の重量B:n−
へブタン抽出前の重量 本発明においては、フルモールド用模型材料としては、
高密度ポリエチレンも用いられるが、この場合、高密度
ポリエチレンとは一般的に低圧法で得られるものであり
、通常、密度0.94g/C1f以上のものが含まれる
R: n-heptane extraction residue ratio A: weight of insoluble matter after 8 hours of n-heptane extraction B: n-
Weight before hebutane extraction In the present invention, as a model material for full mold,
High-density polyethylene is also used, but in this case, high-density polyethylene is generally obtained by a low-pressure method, and usually includes those having a density of 0.94 g/C1f or more.

本発明において、前記ポリプロピレン系樹脂及び高密度
ポリエチレンはそれぞれ単独でも用いられる他1両者を
ブレンドして使用しても良く、ブレンドの場合、そのブ
レンド比率は任意である。
In the present invention, the polypropylene resin and high-density polyethylene may be used alone or in a blend of the two, and in the case of a blend, the blending ratio is arbitrary.

本発明の鋳造用消失模型材料は、前記樹脂粒子を架橋し
、得られた架橋粒子を発泡させて形成した謂ゆる架橋予
備発泡粒子から形成した架橋発泡型内成形体からなるも
のであるが、この場合、架橋粒子は、オートクレーブ中
に、樹脂粒子、水、融着防止剤及び架橋剤を配合し、攪
拌下、樹脂の軟化温度に昇温し、架橋剤を樹脂に含浸さ
せ、その後、架橋温度に昇温保持することにより得られ
る。前記架橋としては、例えば、ジクミルパーオキサイ
ド、1.1−ビス(t−ブチルパーオキシ)3,3゜5
−トリメチルシクロヘキサン、n−ブチル−4,4−ビ
ス(t−ブチルパーオキシ)バレレート、し−ブチルク
ミルパーオキサイド、2,5−ジメチル−2,5−ジ(
t−ブチルパーオキシ)ヘキサン等の有機過酸化物が使
用される。また、ポリプロピレン系樹脂を含む樹脂粒子
の場合は、架橋剤の他に、架橋助剤としてジビニールベ
ンゼンを併用することが好ましい、前記架橋剤の使用量
は、樹脂100重量部に対し、0.05〜5重量部の割
合であり、ジビニールベンゼンの使用量は、樹脂100
重量部に対し。
The disappearing model material for casting of the present invention is composed of a cross-linked and foamed in-mold body formed from so-called cross-linked pre-expanded particles, which are formed by cross-linking the resin particles and foaming the obtained cross-linked particles. In this case, the crosslinked particles are prepared by mixing resin particles, water, an anti-fusing agent, and a crosslinking agent in an autoclave, raising the temperature to the softening temperature of the resin while stirring, impregnating the resin with the crosslinking agent, and then crosslinking. Obtained by raising and maintaining the temperature. Examples of the crosslinking include dicumyl peroxide, 1,1-bis(t-butylperoxy) 3,3°5
-trimethylcyclohexane, n-butyl-4,4-bis(t-butylperoxy)valerate, thi-butylcumyl peroxide, 2,5-dimethyl-2,5-di(
Organic peroxides such as t-butylperoxy)hexane are used. In addition, in the case of resin particles containing polypropylene resin, it is preferable to use divinylbenzene as a crosslinking aid in addition to the crosslinking agent. 05 to 5 parts by weight, and the amount of divinylbenzene used is 100 parts by weight of the resin.
By weight.

0.05〜5重量部の割合である。また、架橋粒子の予
備発泡は、オートクレーブに架橋粒子、水、融着防止剤
、発泡剤を配合し、加圧下、発泡温度まで昇温し、容器
の一端を開放して内容物を低圧帯域に放出させることに
よって行うことができる。
The proportion is 0.05 to 5 parts by weight. In addition, for pre-foaming of cross-linked particles, the cross-linked particles, water, anti-fusing agent, and blowing agent are mixed in an autoclave, the temperature is raised to the foaming temperature under pressure, and one end of the container is opened to transfer the contents to a low-pressure zone. This can be done by releasing it.

この場合、融着防止剤としては、例えば、酸化アルミニ
ウム、酸化チタン、水酸化アルミニウム。
In this case, examples of the anti-fusing agent include aluminum oxide, titanium oxide, and aluminum hydroxide.

塩基性炭酸マグネシウム、塩基性炭酸亜鉛、炭酸亜鉛等
が挙□げられ、発泡剤としては、プロパン、ブタン、ペ
ンタン、トリクロロフロロメタン、ジクロロジフロロメ
タン等の有機系のものの他、二酸化炭素、窒素、空気等
の無機系ガスが挙げられる。
Basic magnesium carbonate, basic zinc carbonate, zinc carbonate, etc. are mentioned, and blowing agents include organic ones such as propane, butane, pentane, trichlorofluoromethane, dichlorodifluoromethane, carbon dioxide, nitrogen, etc. , and inorganic gases such as air.

前記のようにして得られた架橋予備発泡粒子は。The crosslinked pre-expanded particles obtained as described above are as follows.

これを成形用金型内に入れ、加熱発泡させて、架橋発泡
成形体とされ、フルモールド用模型材料として使用され
る。このようにして得られる本発明の架橋発泡型内成形
体の密度は、0.025〜0.012g/c!、好まし
くは0.024〜0.014g/curの範囲内に規定
される。この密度より小さな発泡体ではフルモールド用
模型材料としての機械的強度が弱く不適当であり、一方
、この密度より大きい発泡体では。
This is placed in a mold and heated and foamed to form a crosslinked foam molded product, which is used as a model material for full molding. The density of the crosslinked foamed in-mold body of the present invention thus obtained is 0.025 to 0.012 g/c! , preferably within the range of 0.024 to 0.014 g/cur. Foams with a density smaller than this have weak mechanical strength and are unsuitable as a model material for full molds, while foams with a density larger than this have a weak mechanical strength.

溶湯と接触してガス化する時に、ガス発生量が多くなり
すぎ、湯の吹上げ現像が起きて好ましくない。また、本
発明の架橋発泡型内成形体の架橋度は、ゲル分率o、o
i〜40%に規定するのが好ましい。
When it comes into contact with the molten metal and gasifies, the amount of gas generated is too large, which is undesirable as the hot water blows up and develops. Further, the degree of crosslinking of the crosslinked foamed in-mold body of the present invention is as follows: gel fraction o, o
It is preferable to specify i to 40%.

ゲル分率が40%を超えるようになると、成形体にボイ
ドが多くなるので好ましくない。なお、この場合のゲル
分率は、架橋予備発泡粒子を沸騰キシレンに8時間浸漬
した後に得られる不溶分の割合を示すもので、次の式で
表わされる。
If the gel fraction exceeds 40%, the molded article will have many voids, which is not preferable. The gel fraction in this case indicates the proportion of insoluble matter obtained after immersing the crosslinked pre-expanded particles in boiling xylene for 8 hours, and is expressed by the following formula.

P(%)=−xlOO Pニゲル分率(%) L:架橋予備発泡粒子の重量 M:不溶分の重量 本発明による鋳造用模型は、特別のフルモールド用模型
材料からなるものであり、このものを鋳型の中に埋め、
これに金属の溶湯を注入すると。
P (%) = -xlOO P gel fraction (%) L: Weight of cross-linked pre-expanded particles M: Weight of insoluble matter The casting model according to the present invention is made of a special full-mold model material. bury something in a mold,
When molten metal is poured into this.

その模型はその溶湯と接触して燃焼又は熱分解によりガ
ス化消失され、その模型跡には溶湯が充満される。そし
て、この模型跡に充満された溶湯は。
The model comes into contact with the molten metal and is gasified and eliminated by combustion or thermal decomposition, and the remains of the model are filled with the molten metal. And the molten metal that filled the remains of this model.

そのまま冷却固化されて、模型と同−形状及び寸法の鋳
物が得られる。
It is then cooled and solidified to obtain a casting having the same shape and dimensions as the model.

〔効  果〕〔effect〕

本発明の鋳造用消失模型材料は、前記したようにポリプ
ロピレン系樹脂及び/又は高密度ポリエチレンからなり
、密度が0.025〜0.012g/adである架橋発
泡型内成形体よりなるものであり、注入された溶湯と接
触した時に、容易にガス化され、その際に煤の発生がな
いという特徴を有する上、得られる鋳物は、その表面に
未気化残渣による「ガスじわ」または「波状あれ」等の
表面欠陥や鋳物内部における加炭現象、時には分解ガス
の巻込みによるガス欠陥の発生等の問題がなく、かつ寸
法精度もすぐれている。従って、本発明の鋳造用消失模
型材料を用いて得られる鋳物の場合は、従来の場合とは
異なり、鋳物表面を仕上げ処理するような手間は必要と
されず、そのまま製品とすることができ、著しいコスト
低下を達成することができる。
As described above, the disappearing model material for casting of the present invention is made of a polypropylene resin and/or high-density polyethylene, and is a crosslinked foam molded body having a density of 0.025 to 0.012 g/ad. , when it comes into contact with the injected molten metal, it is easily gasified and no soot is generated at that time, and the resulting casting has ``gas wrinkles'' or ``wavy shapes'' on its surface due to unvaporized residue. There are no problems such as surface defects, carburization inside the casting, or gas defects sometimes caused by entrainment of decomposed gas, and the dimensional accuracy is excellent. Therefore, in the case of a casting obtained using the disappearing model material for casting of the present invention, unlike the conventional case, there is no need to finish the surface of the casting, and it can be used as a product as it is. Significant cost reductions can be achieved.

〔実施例〕〔Example〕

次に本発明を実施例によりさらに詳細に説明する。 Next, the present invention will be explained in more detail with reference to Examples.

実施例1 オートクレーブに、エチレン含有量3.8重量%、n−
ヘプタン抽出残渣割合5%のエチレン−プロピレンラン
ダム共重合体粒子100重量部、水300重量部、融着
防止剤として微粒状の酸化アルミニウム0.3重量部、
架橋剤として1,1−ビス(し−ブチルパーオキシ)−
3,3,5−)−リメチルシクロヘキサン0.30重量
部、ジビニールベンゼン0.3重量部を配合し、攪拌し
ながら100℃に昇温し、この温度に1時間保持した。
Example 1 In an autoclave, ethylene content 3.8% by weight, n-
100 parts by weight of ethylene-propylene random copolymer particles with a heptane extraction residue ratio of 5%, 300 parts by weight of water, 0.3 parts by weight of finely divided aluminum oxide as an anti-fusing agent,
1,1-bis(butylperoxy)- as a crosslinking agent
0.30 parts by weight of 3,3,5-)-limethylcyclohexane and 0.3 parts by weight of divinylbenzene were blended, and the mixture was heated to 100° C. with stirring, and maintained at this temperature for 1 hour.

その後、150℃に昇温し架橋反応を行った後、容器を
いったん冷却し、架橋樹脂粒子を取り出した。
Thereafter, the temperature was raised to 150° C. to perform a crosslinking reaction, and then the container was once cooled and the crosslinked resin particles were taken out.

次に、再度オートクレーブに、前記架橋樹脂粒子100
重量部、水300部、融着防止剤として微粒状の酸化ア
ルミニウム0.3重量部、発泡剤としてジクロワグフロ
ロメタン18!!量部を配合し、攪拌しながら150℃
に昇温し、この温度で15時間保持した後、容器内を空
気で40kg/aJGに加圧しながら容器の一端を開放
し、架橋粒子と水を大気圧下に放出して、発泡を行い、
予備発泡架橋粒子を得た。
Next, the crosslinked resin particles 100 were placed in the autoclave again.
parts by weight, 300 parts of water, 0.3 parts by weight of finely divided aluminum oxide as an anti-fusing agent, and 18 parts by weight of dicrowag fluoromethane as a blowing agent. ! Blend the following amounts and heat to 150°C while stirring.
After raising the temperature to 15 hours and holding it at this temperature for 15 hours, one end of the container was opened while pressurizing the inside of the container with air to 40 kg/aJG, and the crosslinked particles and water were released to atmospheric pressure to perform foaming.
Pre-expanded crosslinked particles were obtained.

次に、この予備発泡架橋粒子を耐圧容器に入れ。Next, the pre-expanded crosslinked particles are placed in a pressure container.

空気にて加圧し、予備発泡架橋粒子内に、 1.5kg
/aIGの粒子内圧を持たせた。この粒子を成形用金型
に入れ、3.2kg/dGの蒸気圧にて加熱発泡させた
後、冷却し、各粒子が融着した発泡成形体、すなわち鋳
造用消失模型材料を得た。
Pressurize with air and place 1.5 kg inside the pre-expanded crosslinked particles.
The particles had an internal pressure of /aIG. The particles were placed in a mold, heated and foamed at a vapor pressure of 3.2 kg/dG, and then cooled to obtain a foamed molded article in which each particle was fused, that is, a disappearing model material for casting.

実施例2 実施例1において、エチレン含有量2.8重量%。Example 2 In Example 1, the ethylene content was 2.8% by weight.

n−ヘプタン抽出残渣割合28%のエチレン−プロピレ
ンランダム共重合体粒子を用いると共に、架横側の量を
0.35重量部、ジビニールベンゼン0.35重量部、
ジクロロンフロロメタン19重量部にした以外は実施例
1と同様にして、鋳造用消失模型材料を得た。
Ethylene-propylene random copolymer particles with an n-heptane extraction residue ratio of 28% were used, and the amount on the cross side was 0.35 parts by weight, divinylbenzene 0.35 parts by weight,
A vanishing model material for casting was obtained in the same manner as in Example 1 except that 19 parts by weight of dichlorofluoromethane was used.

実施例3 実施例1において、エチレン含有量1.5重量%、n−
へブタン抽出残液割合40%のエチレン−プロピレンラ
ンダム共重合体粒子を用いると共に、架橋剤の量を0.
25重量部、ジビニールベンゼン0.25重量部、ジク
ロロンフロロメタ220重量部にした以外は実施例1と
同様にして、鋳造用消失模型材料を得た。
Example 3 In Example 1, the ethylene content was 1.5% by weight, n-
Ethylene-propylene random copolymer particles with a hebutane extraction residue ratio of 40% were used, and the amount of crosslinking agent was 0.
A vanishing model material for casting was obtained in the same manner as in Example 1, except that the amounts were 25 parts by weight, 0.25 parts by weight of divinylbenzene, and 220 parts by weight of dichloromethane.

実施例4 オートクレーブに、密度0.958g/cd、 XI(
メルトインデックス)0.40の高密度ポリエチレン粒
子100重量部、水300重量部微粒状の酸化アルミニ
ウム0゜3重量部、架橋剤としてジクミルパーオキサイ
ド0゜32重量部を配合し、攪拌しながら、100℃に
昇温し、この温度で1時間保持した。その後、150℃
に昇温して90分間保持した後、容器を冷却し、架橋樹
脂粒子を取り出した。
Example 4 In an autoclave, XI (density 0.958 g/cd,
100 parts by weight of high-density polyethylene particles with a melt index of 0.40, 300 parts by weight of water, 0.3 parts by weight of finely divided aluminum oxide, and 0.32 parts by weight of dicumyl peroxide as a crosslinking agent were mixed, and while stirring, The temperature was raised to 100°C and maintained at this temperature for 1 hour. After that, 150℃
After raising the temperature to 90 minutes and holding it for 90 minutes, the container was cooled and the crosslinked resin particles were taken out.

次に、再度オートクレーブに、架橋樹脂粒子100重量
部、水300重量部、微粒状の酸化アルミニウム0.3
重量部、ジクロロンフロロメタン28重量部を配合し、
攪拌しながら150℃に昇温し、その温度で15分間保
持した後、容器内を空気で40kg/dGに加圧しなが
ら容器の一端を開放し、架橋樹脂粒子と水を大気圧下に
放出し発泡を行い、予備発泡架橋粒子を得た。
Next, 100 parts by weight of crosslinked resin particles, 300 parts by weight of water, and 0.3 parts of fine aluminum oxide were placed in the autoclave again.
parts by weight, 28 parts by weight of dichlorofluoromethane,
The temperature was raised to 150°C while stirring, and after holding at that temperature for 15 minutes, one end of the container was opened while pressurizing the inside of the container to 40 kg/dG with air, and the crosslinked resin particles and water were released to atmospheric pressure. Foaming was performed to obtain pre-foamed crosslinked particles.

次に、得られた予備発泡架橋粒子を耐圧容器に入れ、空
気にて加圧し5粒子に1.5kg/CiGの粒子内圧を
もたせた。この粒子を成形用金型に入れ、3.2kg/
alGの蒸気圧にて加熱し1発泡させた後。
Next, the obtained pre-expanded crosslinked particles were placed in a pressure container and pressurized with air to give 5 particles an internal pressure of 1.5 kg/CiG. The particles were put into a mold and weighed 3.2 kg/
After heating at the vapor pressure of alG and foaming.

冷却し1粒子が相互に融着した発泡成形体、即ち。A foamed molded product in which particles are fused to each other after cooling.

鋳造用消失模型材料を得た。A vanishing model material for casting was obtained.

実施例5 実施例4において、密度0.952g/a#、 MIo
、11の高密度ポリエチレン粒子を用いると共に、架橋
剤の量を0.30重量部、ジクロロジフロロメタン量を
25重量部にした以外は、実施例4と同様にして鋳造用
消失模型材料を得た。
Example 5 In Example 4, density 0.952 g/a#, MIo
A vanishing model material for casting was obtained in the same manner as in Example 4, except that high-density polyethylene particles of No. Ta.

実施例6 実施例4において、密度0.968g/aj、 MI5
.5の高密度ポリエチレン粒子を用いると共に、架橋剤
の量を0.28重量部、ジクロロジフロロメタン量を3
0重量部にした以外は実施例4と同様にして鋳造用消失
模型材料を得た。
Example 6 In Example 4, density 0.968 g/aj, MI5
.. In addition to using high-density polyethylene particles of No. 5, the amount of crosslinking agent was 0.28 parts by weight, and the amount of dichlorodifluoromethane was 3 parts by weight.
A vanishing model material for casting was obtained in the same manner as in Example 4 except that the amount was 0 parts by weight.

実施例7 実施例1において、エチレン含有量2.8重量%、n−
へブタン抽出残液割合28%のエチレン−プロピレンラ
ンダム共重合体30重量%と、密度0.958g/cj
、MIo、4の高密度ポリエチレン70重量%のブレン
ド粒子を用いると共に、架橋剤としてジクミルパーオキ
サイド0.35重量部、ジビニールベンゼン0.35重
量部、ジクロロジフロロメタン量を23重量部にした以
外は実施例1と同様にして鋳造用消失模型材料を得た。
Example 7 In Example 1, the ethylene content was 2.8% by weight, n-
30% by weight of ethylene-propylene random copolymer with hebutane extraction residual liquid ratio of 28% and density of 0.958 g/cj
, MIo, 70% by weight of high-density polyethylene blend particles of 4 were used, and the crosslinking agent was 0.35 parts by weight of dicumyl peroxide, 0.35 parts by weight of divinylbenzene, and the amount of dichlorodifluoromethane was 23 parts by weight. A vanishing model material for casting was obtained in the same manner as in Example 1 except for the following.

実施例8 実施例1において、エチレン含有量2.8重量%、n−
へブタン抽出残渣割合30%のエチレン−プロピレンラ
ンダム共重合体70重量%と、密度0.954g/cd
、 MI 2の高密度ポリエチレン30重量%のブレン
ド粒子を用いると共に、ジクロロジフロロメタン量を2
0重量部にした以外は実施例1と同様にして鋳造用消失
模型材料を得た。
Example 8 In Example 1, the ethylene content was 2.8% by weight, n-
70% by weight of ethylene-propylene random copolymer with hebutane extraction residue ratio of 30% and density of 0.954 g/cd
, using blend particles of 30% by weight of high-density polyethylene of MI 2, and the amount of dichlorodifluoromethane was 2.
A vanishing model material for casting was obtained in the same manner as in Example 1 except that the amount was 0 parts by weight.

比較例1 オートクレーブに、実施例2で示した架橋粒子100重
量部、水300重量部、微粒状の酸化アルミニウム0.
3重量部、ジクロロンフロロメタ216重量部を配合し
、攪拌しながら150℃に昇温し、その温度で15分間
保持した後、容器内を空気で40kg/cdGに加圧し
ながら容器の一端を開放し、架橋粒子と水を大気圧下に
放出し発泡を行い、予備発泡架橋粒子を得た。
Comparative Example 1 In an autoclave, 100 parts by weight of the crosslinked particles shown in Example 2, 300 parts by weight of water, and 0.0 parts by weight of finely divided aluminum oxide were added.
3 parts by weight and 216 parts by weight of dichlorone fluorometa were mixed, heated to 150°C while stirring, held at that temperature for 15 minutes, and then closed one end of the container while pressurizing the inside of the container to 40 kg/cdG with air. The container was opened, and the crosslinked particles and water were discharged under atmospheric pressure to perform foaming, thereby obtaining pre-foamed crosslinked particles.

次に、得られた予備発泡架橋粒子を耐圧容器に入れ、空
気にて加圧し、発泡粒子内に1.5kg/c+JGの粒
子内圧を持たせた。この粒子を成形用金型に入れ、3.
2kg/aJGの蒸気圧にて加熱発泡させた後。
Next, the obtained pre-foamed crosslinked particles were placed in a pressure container and pressurized with air to give an internal pressure of 1.5 kg/c+JG within the expanded particles. Place the particles into a mold for molding; 3.
After heating and foaming at a steam pressure of 2 kg/aJG.

冷却し、各粒子相互が融着した発泡成形体、即ち。A foam molded product in which each particle is fused together after cooling.

鋳造用消失模型材料を得た。A vanishing model material for casting was obtained.

比較例2 比較例1で得られた予備発泡架橋粒子を耐圧容器中で空
気加圧し1発泡粒子内に空気で約3kg/cdGの内圧
を持たせた。この粒子を1.3kg/aJGの蒸気にて
加熱して、カサ密度0.01g/ciiの発泡粒子を得
た。
Comparative Example 2 The pre-expanded crosslinked particles obtained in Comparative Example 1 were pressurized with air in a pressure-resistant container so that each expanded particle had an internal pressure of about 3 kg/cdG of air. The particles were heated with steam at 1.3 kg/aJG to obtain expanded particles with a bulk density of 0.01 g/cii.

この粒子を耐圧容器中にみれ、空気で加圧し、発泡粒子
内に1.5kg/aJGの粒子内圧を持たせた。この粒
子を成形用金型に入れ、 3.2kg/a#Gに蒸気に
て加熱発泡させた後、冷却し、各粒子相互が融着した発
泡成形体、即ち、鋳造用消失模型材料を得た。
The particles were placed in a pressure-resistant container and pressurized with air to give the expanded particles an internal pressure of 1.5 kg/aJG. These particles were placed in a mold, heated and foamed with steam to 3.2 kg/a#G, and then cooled to obtain a foam molded product in which each particle was fused to each other, that is, a disappearing model material for casting. Ta.

比較例3 実施例4において、ジクロロジフロロメタン量を25重
量部にした以外は同様にして鋳造用消失模型材料を得た
Comparative Example 3 A vanishing model material for casting was obtained in the same manner as in Example 4, except that the amount of dichlorodifluoromethane was changed to 25 parts by weight.

比較例4 実施例4で示した予備発泡架橋粒子を耐圧容器中で加圧
し1発泡粒子内に空気で約2kg/aJGの内圧を持た
せた。この粒子を1.5kg/aJGの蒸気にて加熱発
泡させ、カサ密度0.01g/cIlの第2予備発泡架
橋粒子を得た。この粒子を耐圧容器中に入れ、空気で加
圧し発泡粒子内に1.5kg/dGの粒子内圧を持たせ
た。この粒子を成形用金型に入れ、3.2kg/aiG
の蒸気にて加熱発泡させた後、冷却し、各粒子相互が融
着した発泡成形体、即ち、鋳造用消失模型材料を得た。
Comparative Example 4 The pre-expanded crosslinked particles shown in Example 4 were pressurized in a pressure-resistant container so that each expanded particle had an internal pressure of about 2 kg/aJG of air. These particles were heated and foamed with steam at 1.5 kg/aJG to obtain second pre-expanded crosslinked particles having a bulk density of 0.01 g/cIl. The particles were placed in a pressure-resistant container and pressurized with air to provide an internal pressure of 1.5 kg/dG within the expanded particles. The particles were put into a mold and weighed 3.2 kg/aiG.
After heating and foaming with steam, the mixture was cooled to obtain a foamed molded product in which each particle was fused to each other, that is, a disappearing model material for casting.

次に、前記のようにして得た消失模型材料を用いて1図
面に示す如き形状の模型を作成し、Mh。
Next, using the vanishing model material obtained as described above, a model having a shape as shown in Figure 1 was created, and Mh.

系塗型を発泡粒子が肉眼的に見えなくなるまで全面に塗
布した後、湯口系と共に鋳型(フラン物を使用)内に埋
め、湯口上に設けた掛堰より鋳鉄溶湯(炭素3.24重
量%、珪素2.7重量%、マンガン0゜65重量%、残
部鉄及び不純物)を鋳込温度1350℃で鋳込んで鋳物
を製作し、この鋳物の品質評価を行った。一方、鋳鋼溶
湯(炭素0.18重量%、珪素0゜40重量%、マンガ
ン0.70重量%、残部鉄及び不純物)を鋳込む場合に
は、同一模型(塗型としてはジルコン粉末を基材とする
塗型を用い、これを上記と同様に塗布した)上に直径5
0m■X高さ50w+mの盲押湯を設けた鋳型に153
0℃で鋳込み、品質評価の欠陥としては鋳物内部におけ
る加炭並びにガス欠陥の有無を判定した。その結果を次
表に示す。
After applying the system coating to the entire surface until the foamed particles are no longer visible to the naked eye, it is buried in the mold (furan material is used) together with the sprue system, and molten cast iron (carbon 3.24% by weight) is poured through a weir installed above the sprue. , 2.7% by weight of silicon, 0.65% by weight of manganese, and the balance iron and impurities) were cast at a casting temperature of 1350° C., and the quality of this casting was evaluated. On the other hand, when casting molten cast steel (0.18% by weight of carbon, 0.40% by weight of silicon, 0.70% by weight of manganese, balance iron and impurities), the same model (the coating mold is based on zircon powder) This was applied in the same manner as above using a coating mold with a diameter of 5 mm.
153 in a mold with a blind feeder of 0m x height 50w+m
It was cast at 0° C., and the presence or absence of carburization and gas defects inside the casting was determined as quality evaluation defects. The results are shown in the table below.

なお、表中に示した品質評価において、「炭素残液」は
、鋳造物表面に付着する炭素残渣の有無を判定したもの
であり、「欠陥」は、鋳物表面における「ガスじわ」、
「波状あれ」又は「ガス欠陥」、鋳物内部における「ガ
ス欠陥」、「加炭の発生」の有無を判定したものであり
、「変形」は、模型寸法と比較した時に、鋳物の形状、
寸法に変形が見られるか否かを判定したものである。
In the quality evaluation shown in the table, "carbon residue" refers to the presence or absence of carbon residue adhering to the surface of the casting, and "defects" refer to "gas wrinkles" on the surface of the casting.
The presence or absence of "wavyness" or "gas defects", "gas defects" inside the casting, or "occurrence of carburization" is determined. "Deformation" refers to the shape of the casting when compared with the model dimensions.
It is determined whether or not there is any deformation in the dimensions.

また、図面において示した模型において、寸法a : 
200mm、 b : 30w+m、 c : 30n
++w、 d : 30+sm、 e : 200mm
In addition, in the model shown in the drawing, the dimension a:
200mm, b: 30w+m, c: 30n
++w, d: 30+sm, e: 200mm
.

f : 200mmである。f: 200mm.

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

図面は鋳込試験で用いた模型を示し、そのA図は正面図
、B図は平面図を示す。 特許出願人 日本スチレンペーパー株式会社(ほか1名
The drawings show the model used in the casting test, of which figure A shows a front view and figure B shows a plan view. Patent applicant: Nippon Styrene Paper Co., Ltd. (and one other person)

Claims (4)

【特許請求の範囲】[Claims] (1)構成する樹脂がポリプロピレン系樹脂及び/又は
高密度ポリエチレンからなり、密度が0.025〜0.
012g/cm^3である架橋発泡型内成形体よりなる
ことを特徴とする鋳造用消失模型材料。
(1) The constituent resin is made of polypropylene resin and/or high-density polyethylene, and has a density of 0.025 to 0.
1. A vanishing model material for casting, characterized in that it is made of a cross-linked foamed in-mold body having a weight of 0.012 g/cm^3.
(2)ポリプロピレン系樹脂がエチレン含有量1〜10
重量%のエチレン−プロピレンランダム共重合体よりな
る特許請求の範囲第1項記載の鋳造用消失模型材料。
(2) Polypropylene resin has an ethylene content of 1 to 10
% by weight of an ethylene-propylene random copolymer, as claimed in claim 1.
(3)ポリプロピレン系樹脂のn−ヘプタン抽出残渣割
合が50%以下である特許請求の範囲第1項又は第2項
記載の鋳造用消失模型材料。
(3) The disappearing model material for casting according to claim 1 or 2, wherein the n-heptane extraction residue ratio of the polypropylene resin is 50% or less.
(4)架橋発泡型内成形体のゲル分率が0.01%〜4
0%である特許請求の範囲第1項又は第2項記載の鋳造
用消失模型材料。
(4) Gel fraction of cross-linked foamed in-mold body is 0.01% to 4
The disappearing model material for casting according to claim 1 or 2, which has a content of 0%.
JP3987385A 1985-02-27 1985-02-28 Consumable pattern material for casting Granted JPS61199545A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP3987385A JPS61199545A (en) 1985-02-28 1985-02-28 Consumable pattern material for casting
DE8686301032T DE3675042D1 (en) 1985-02-27 1986-02-14 MOLDING PROCESS.
EP86301032A EP0195512B1 (en) 1985-02-27 1986-02-14 Casting method
US06/830,730 US4711287A (en) 1985-02-27 1986-02-19 Casting method
CA000502477A CA1248322A (en) 1985-02-27 1986-02-21 Casting method using consumable pattern

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3987385A JPS61199545A (en) 1985-02-28 1985-02-28 Consumable pattern material for casting

Publications (2)

Publication Number Publication Date
JPS61199545A true JPS61199545A (en) 1986-09-04
JPH0318532B2 JPH0318532B2 (en) 1991-03-12

Family

ID=12565097

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3987385A Granted JPS61199545A (en) 1985-02-27 1985-02-28 Consumable pattern material for casting

Country Status (1)

Country Link
JP (1) JPS61199545A (en)

Also Published As

Publication number Publication date
JPH0318532B2 (en) 1991-03-12

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