JPS6284853A - Material for casting pattern - Google Patents

Material for casting pattern

Info

Publication number
JPS6284853A
JPS6284853A JP22655385A JP22655385A JPS6284853A JP S6284853 A JPS6284853 A JP S6284853A JP 22655385 A JP22655385 A JP 22655385A JP 22655385 A JP22655385 A JP 22655385A JP S6284853 A JPS6284853 A JP S6284853A
Authority
JP
Japan
Prior art keywords
crosslinked
mold
foam
particles
density
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
JP22655385A
Other languages
Japanese (ja)
Other versions
JPH0456699B2 (en
Inventor
Hideki Kuwabara
英樹 桑原
Masato Naito
真人 内藤
Tadatsugu Hamada
浜田 忠嗣
Teishiro Watanabe
渡辺 貞四郎
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 JP22655385A priority Critical patent/JPS6284853A/en
Publication of JPS6284853A publication Critical patent/JPS6284853A/en
Publication of JPH0456699B2 publication Critical patent/JPH0456699B2/ja
Granted legal-status Critical Current

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  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Molds, Cores, And Manufacturing Methods Thereof (AREA)

Abstract

PURPOSE:To obtain a material having excellent cutting workability and parting characteristic for a casting pattern by foam molding a crosslinked PE resin particles which is formed of a HDPE resin and having a limited gel fraction in a mold integrally. CONSTITUTION:The material for the casting pattern consists of the foamed material formed by foam molding the crosslinked PE resin particles having <=50% gel fraction in the mold and the density thereof is limited to 0.2-0.022g/cm<3> and the average cell size to a 70-1,000mum range. The workability is deteriorated if the density exceeds the above-mentioned range and the dimensional stability is deteriorated if the range is below the range. The crosslinked PE resin particles used as the material for the casting pattern is formed of the HDPE resin.

Description

【発明の詳細な説明】 〔技術分野〕 本発明は、架橋ポリエチレン系樹脂予備発泡粒子の型内
発泡成形体を主原料とした鋳造模型用材料に関し、さら
に詳しくは、微細な気泡系とすぐれた表面硬度を有する
架橋ポリエチレン系樹脂予備発泡粒子の型内発泡成形体
を主原料とした鋳造模型用材料に関するものである。
[Detailed Description of the Invention] [Technical Field] The present invention relates to a material for casting models that is made mainly from an in-mold foam molded product of cross-linked polyethylene resin pre-expanded particles, and more specifically, it relates to a material for a casting model that is made mainly from an in-mold foamed product made of pre-expanded particles of a cross-linked polyethylene resin. The present invention relates to a material for casting models whose main raw material is an in-mold foamed product of pre-expanded crosslinked polyethylene resin particles having surface hardness.

〔従来技術〕[Prior art]

従来から鋳造模型用材料としては木材が主原料として使
用され、現在でも慣習的に杉などの木材が一般的に使わ
れている。木材は表面硬度が大きく、成型時の寸法安定
性がすぐれる等の特性を備えているが、その反面1価格
が高いこと、乾燥が必要なこと1節や木目があるため加
工成形に非常な熟練を要すること、木材では重量が大き
いため運搬に不便であること、保存時に変形が生じた場
合、使用の都度修正をほどこす必要があるなどの欠点を
有しているゆ 鋳造用木材に見られる以上のような欠点から、近年では
、ポリスチレンの型内発泡成形体を鋳造模型用材料に用
いる試みがなされている。しかし、ポリスチレン発泡成
形体は前述した木材の欠点は解決するものの、逆に、発
泡ポリスチレンの本来の性質上、脆いという欠点を有す
ることから、木工用工具による加工において、引っかき
キズがつき易い等の加工上の問題点を有している。
Traditionally, wood has been used as the main material for casting models, and even now, wood such as cedar is commonly used. Wood has characteristics such as high surface hardness and excellent dimensional stability during molding, but on the other hand, it is expensive, requires drying, and has knots and grain, making it extremely difficult to process and mold. Wood for casting has disadvantages such as requiring skill, being heavy and inconvenient to transport, and needing to be modified each time it is used if it becomes deformed during storage. Due to the above-mentioned drawbacks, attempts have been made in recent years to use in-mold foam molded products of polystyrene as materials for casting models. However, although polystyrene foam moldings solve the above-mentioned drawbacks of wood, they also have the disadvantage of being brittle due to the inherent nature of foamed polystyrene, so they are easily scratched when processed with woodworking tools. It has processing problems.

特公昭47−43404号公報には、前記木材に見られ
る欠点を解消するものとして、特定の方法で加橋発泡し
て得られたゲル分率30〜90%、カサ密度0.5−0
.05g/c+J、平均気泡径が400 μm以下の結
晶性ポリオレフィン樹脂架橋発泡体からなる鋳造用模型
材料が示されている。しかしながら、この発泡体は1発
泡剤として熱分解型のアミド類を使用する為に、密度を
小さくしようとすると発泡剤を多く使用せねばならず精
密な鋳造物の生産には使用できなく、しかも、いまだに
吸水率が多いという欠点を有し、そのため砂との離型性
が悪く実際に使われていないのが現実である。
Japanese Patent Publication No. 47-43404 discloses a material with a gel fraction of 30 to 90% and a bulk density of 0.5 to 0, which is obtained by cross-linking and foaming using a specific method, as a material that eliminates the defects found in the above-mentioned wood.
.. 05g/c+J, and a casting pattern material made of a crystalline polyolefin resin crosslinked foam having an average cell diameter of 400 μm or less. However, this foam uses a pyrolytic amide as one blowing agent, so if you try to reduce the density, you have to use a lot of blowing agent, and it cannot be used to produce precision castings. However, the reality is that it still has the disadvantage of high water absorption and therefore poor releasability from sand, so it is not actually used.

〔目   的〕〔the purpose〕

本発明は、従来の鋳造模型用発泡体に見られる前記欠点
を克服し1寸法精度の良好な鋳造物を与える吸水率の小
さな模型保管時変形がない鋳造模型用発泡体を提供する
ことを目的とする。
An object of the present invention is to overcome the above-mentioned drawbacks of conventional foams for casting models, and to provide a foam for casting models that has a low water absorption rate and does not deform when the model is stored, which provides castings with good one-dimensional accuracy. shall be.

〔構  成〕〔composition〕

本発明は、ゲル分率20〜40%の架橋ポリエチレン系
樹脂粒子を型内に一体に発泡成形した架橋ポリエチレン
系樹脂型内発泡成形体からなり、密度0.2〜0.02
2g/crl、平均気泡径70〜1000μmを有し。
The present invention consists of a cross-linked polyethylene resin in-mold foam molded product in which cross-linked polyethylene resin particles with a gel fraction of 20 to 40% are integrally foam-molded in a mold, and the density is 0.2 to 0.02.
2 g/crl and an average cell diameter of 70 to 1000 μm.

かつ前記架橋ポリエチレン系樹脂粒子は、高密度ポリエ
チレン系樹脂から形成されていることを特徴とする鋳造
模型用材料を要旨とする。
The crosslinked polyethylene resin particles are made of a high density polyethylene resin.

本発明の鋳造模型用材料は、ゲル分率が50%以下の架
橋ポリエチレン系樹脂予備発泡粒子を型内において発泡
成形させて形成した発泡体からなるものである。この場
合、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。
The casting model material of the present invention is made of a foam formed by foam-molding crosslinked polyethylene resin pre-expanded particles having a gel fraction of 50% or less in a mold. In this case, the gel fraction is 8% when the cross-linked pre-expanded particles are placed in boiling xylene.
This indicates the percentage of insoluble matter obtained after soaking for a period of time.
It is expressed by the following formula.

P (%)=−X100 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 前記ゲル分率が50%を超えるようになると、成形体に
ボイド形成が多くなり、又吸水率が多くなるので好まし
くなく、架橋樹脂予備発泡粒子のゲル分率は、好ましく
は20〜40%に規定するのがよい。
P (%) = -X100 P gel fraction (%) L: Weight of crosslinked pre-expanded particles M: Weight of insoluble matter If the gel fraction exceeds 50%, void formation will increase in the molded body, Moreover, it is not preferable because the water absorption rate increases, and the gel fraction of the crosslinked resin pre-expanded particles is preferably set to 20 to 40%.

また、本発明の鋳造模型用材料として用いる前記予備発
泡粒子の型内発泡成形体において、その密度(カサ密度
)は0.2〜0.022g/aJ、好ましくは0.14
〜0.03g/cjの範囲に規定され、またその平均気
泡径は70〜1000μm、好ましくは80〜900μ
園の範囲に規定される。発泡体の密度が前記範囲より大
きくなると、機械的強度が高く、寸法安定性は増すもの
の、逆に加工性が悪化し、また重量も重くなるので好ま
しくなく、一方、前記範囲より小さくなると、軽量化の
点ではすぐれるものの5発泡体が柔軟になり1寸法安定
性に劣るようになるので好ましくない。本発明の場合、
発泡体の圧縮硬さくJIS K−6767)は、一般的
には、0.7kg/cj以上に規定するのがよい。また
、発泡体の平均気泡径が前記範囲より小さくなると、発
泡体の切断加工が難かしくなると共に、切断品の表面状
態がセル膜の破れにより悪くなるので好ましくなく、一
方、前記範囲より大きくなると、この場合も切断面の表
面状態に荒れが生じたり、また吸水率が高くなる等の難
点が生じるので好ましくない。
Further, in the in-mold foamed product of the pre-expanded particles used as the casting model material of the present invention, its density (bulk density) is 0.2 to 0.022 g/aJ, preferably 0.14 g/aJ.
-0.03g/cj, and the average bubble diameter is 70-1000μm, preferably 80-900μm.
It is defined in the scope of the garden. If the density of the foam is larger than the above range, the mechanical strength will be high and the dimensional stability will increase, but workability will deteriorate and the weight will also increase, which is undesirable. On the other hand, if the density is smaller than the above range, the weight will increase Although it is excellent in terms of flexibility, it is not preferable because the foam becomes flexible and has poor one-dimensional stability. In the case of the present invention,
The compression hardness of the foam (JIS K-6767) is generally preferably set to 0.7 kg/cj or more. Furthermore, if the average cell diameter of the foam is smaller than the above range, it becomes difficult to cut the foam and the surface condition of the cut product deteriorates due to tearing of the cell membrane, which is undesirable. In this case as well, problems such as roughness of the cut surface and increased water absorption occur, which is not preferable.

本発明の鋳造模型用材料として用いるポリエチレン系樹
脂は、密度0.945g/cj以上、好ましくは密度0
.950〜0.970g/aJの高密度ポリエチレン系
樹脂である。低密度ポリエチレン系樹脂では、同じ強度
の発泡体を得ようとすると重量が重くなり、その結果、
コストも高くなるので好ましくない。
The polyethylene resin used as the casting model material of the present invention has a density of 0.945 g/cj or more, preferably a density of 0.
.. It is a high density polyethylene resin with a weight of 950 to 0.970 g/aJ. With low-density polyethylene resin, if you try to obtain a foam with the same strength, it will be heavier;
This is not preferable because it increases the cost.

本発明の鋳造模型用材料は、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型内架橋発泡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。
The cast model material of the present invention is an in-mold crosslinked foamed molded product formed from so-called crosslinked pre-expanded particles, which are formed by crosslinking the resin particles and foaming the obtained crosslinked particles. If the crosslinked particles are autoclaved,
Mix resin particles, water, an anti-fusing agent, and a cross-linking agent, raise the temperature to the softening temperature of the resin while stirring, and impregnate the resin with the cross-linking agent.
Thereafter, it is obtained by raising and maintaining the temperature at the crosslinking temperature.

前記架橋としては1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(
七−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(し−
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、これらの架橋剤には、架橋助剤としてジビ
ニールベンゼンを併用することもできる。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 crosslinking includes 1, for example, dicumyl peroxide,
1,1-bis(t-butylperoxy)3,3.5-trimethylcyclohexane, n-butyl-4,4-bis(
7-butylperoxy)valerate, 7-butylcumyl peroxide, 2,5-dimethyl-2,5-di(7-butylperoxy)valerate, 2,5-dimethyl-2,5-di(7-butylperoxy)valerate
Organic peroxides such as butylperoxy)hexane are used. Moreover, divinylbenzene can also be used together with these crosslinking agents as a crosslinking aid. The amount of the crosslinking agent used is 0.05 to 5 parts by weight per 100 parts by weight of the resin, and the amount of divinylbenzene used is per 100 parts by weight of the resin.

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
1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, to pre-foam the crosslinked particles, mix the crosslinked particles, water, anti-fusing agent, and blowing agent in an autoclave, raise the temperature to the foaming temperature under pressure, open one end of the container, and 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、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揮発性
有機発泡剤の他、二酸化炭素、窒素、空気等の無機系ガ
スが挙げられる。
In this case, examples of the anti-fusing agent include aluminum oxide, titanium oxide, aluminum hydroxide, basic magnesium carbonate, basic zinc carbonate, zinc carbonate, etc.
Examples of the blowing agent include volatile organic blowing agents such as propane, butane, pentane, trichlorofluoromethane, and dichlorodifluoromethane, as well as inorganic gases such as carbon dioxide, nitrogen, and air.

前記のようにして得られた予備発泡粒子は、これを耐圧
容器中で空気を加圧し1粒子内に0.5〜3kg/cn
T程度の粒子内圧を持たせた後、成形成金型内に入れ、
加熱発泡により、一体に成形し1発泡成形体となし、次
いで冷却して金型から取出す。
The pre-expanded particles obtained as described above are pressurized with air in a pressure-resistant container to give a concentration of 0.5 to 3 kg/cn per particle.
After giving the particles an internal pressure of about T, put them into a forming mold,
By heating and foaming, the product is molded into a single foam molded product, which is then cooled and taken out from the mold.

このようにして得た架橋ポリエチレン系樹脂型内発泡成
形体を乾燥し、鋳造模型用材料として使用する。
The crosslinked polyethylene resin in-mold foam molded product thus obtained is dried and used as a material for a casting model.

〔効  果〕〔effect〕

本発明の鋳造模型用材料は、前記した特定の発泡体から
なるもので、使来の木材や、発泡体からなるものと同様
に使用されるが1本発明で用いる発泡体は、切断加工性
にすぐれるため、従来の木材原型を製造する場合に用い
た工具がそのまま使用できる利点がある上、表面平滑で
かつ高い圧縮硬さを有し、さらに有利なことには、吸水
率の著しく小さなものであることから、寸法安定性にす
ぐれた鋳造用原型を与える。また、本発明の鋳造模型用
材料は、圧縮硬さが高くかつ吸水率の小さなものである
ことから、離型性に著しくすぐれたものである。
The casting model material of the present invention is made of the above-mentioned specific foam, and can be used in the same way as conventional wood or foam. It has the advantage of being able to use the tools used to produce conventional wood patterns as is, and has a smooth surface and high compressive hardness, and even more advantageously, has extremely low water absorption. Because it is a material, it provides a mold for casting with excellent dimensional stability. Furthermore, the casting model material of the present invention has high compressive hardness and low water absorption, so it has extremely excellent mold releasability.

〔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.

〔評価基準〕〔Evaluation criteria〕

(1)切断加工の雌品度: 0・・・切断時に抵抗がなくスムースに切断できる。 (1) Female quality of cutting process: 0: Smooth cutting with no resistance during cutting.

Δ・・・切断時に抵抗はあるが一応切断できる。Δ...There is some resistance when cutting, but it is possible to cut.

X・・・切断時に抵抗が大きく振動を発生する。X: The resistance is large and vibrations occur during cutting.

(2)切断品の表面状態: O・・・表面が滑らか。(2) Surface condition of cut product: O...Surface is smooth.

△・・・表面に若干荒れがある。△...The surface is slightly rough.

X・・・表面に荒れかつもげる粒子がある。X: There are particles that are rough and peeling on the surface.

(3)圧縮カタサ(JIS−に−6767に準拠):0
=−0,1kg/a!以上 X・・・0.7g10(未満 (4)吸水率(JIS −K −6767B法):○・
・−0,003g/cn?未満 △−−−0.03−0.003g/cn(X・・・0.
03g/cd以上 実施例、比較例 オートクレーブに第1表に示す密度、 MI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
ルパーオキサイドを第1表に示す量、又、比較例1にお
いては、ジビニールベンゼンを0.4重量部追加配合し
、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℃に昇温しで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。
(3) Compression flatness (based on JIS-6767): 0
=-0.1kg/a! More than X...0.7g10 (less than (4) Water absorption rate (JIS-K-6767B method):○・
・-0,003g/cn? Less than △---0.03-0.003g/cn (X...0.
03 g/cd or more Examples and Comparative Examples The autoclave had the density shown in Table 1, 100 parts by weight of MI high-density polyethylene particles, 300 parts by weight of water, 0.3 parts by weight of finely divided aluminum oxide, and dicumyl per as a crosslinking agent. The amount of oxide shown in Table 1 was added, and in Comparative Example 1, 0.4 part by weight of divinylbenzene was added, the temperature was raised to 100° C. with stirring, and the temperature was maintained at this temperature for 1 hour. Thereafter, the temperature was raised to 150°C and held for 90 minutes, and then 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、ジクロロジフロロメタンを第1表に示す量配合し、
攪拌しながら昇温し、第1表に示す9!泡温度に15分
間保持した。その後容器内を空気で40kg/cnfG
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 were added to the autoclave again.
300 parts by weight of water, 0.3 parts by weight of finely divided aluminum oxide, and dichlorodifluoromethane were blended in the amounts shown in Table 1,
The temperature was raised while stirring, and the temperature was increased to 9! shown in Table 1. Hold at foam temperature for 15 minutes. After that, the inside of the container is filled with air at 40kg/cnfG.
While pressurizing the container, one end of the container was opened, and the crosslinked resin particles and water were released under atmospheric pressure to perform foaming, thereby obtaining pre-foamed crosslinked particles.

次に得られた予備発泡粒子を耐圧容器に入れ、空気にて
加圧し、粒子に1.5kg/cJGの粒子内圧をもたせ
た。この粒子を成形成金型に入れ3.2kg/c+JG
の蒸気圧にて加熱し1g!泡させた後、冷却し、粒子が
相互に融着した発泡成形体、即ち鋳造模型用材料を得た
Next, the obtained pre-expanded particles were placed in a pressure container and pressurized with air to give the particles an internal pressure of 1.5 kg/cJG. Put these particles into a forming mold and weigh 3.2kg/c+JG
Heated with steam pressure of 1g! After foaming, the mixture was cooled to obtain a foam molded product in which the particles were fused to each other, that is, a material for a casting model.

Claims (1)

【特許請求の範囲】[Claims] (1)ゲル分率50%以下の架橋ポリエチレン系樹脂粒
子を型内にて一体に発泡成形した架橋ポリエチレン系樹
脂型内発泡成形体からなり、密度0.2〜0.02g/
cm^3、平均気泡径70〜1000μmを有し、かつ
前記架橋ポリエチレン系樹脂粒子は、高密度ポリエチレ
ン樹脂から形成されていることを特徴とする鋳造模型用
材料。
(1) Consists of a cross-linked polyethylene resin in-mold foam molded product made by integrally foam-molding cross-linked polyethylene resin particles with a gel fraction of 50% or less in a mold, and has a density of 0.2 to 0.02 g/
cm^3 and an average cell diameter of 70 to 1000 μm, and the crosslinked polyethylene resin particles are made of high-density polyethylene resin.
JP22655385A 1985-10-09 1985-10-09 Material for casting pattern Granted JPS6284853A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22655385A JPS6284853A (en) 1985-10-09 1985-10-09 Material for casting pattern

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22655385A JPS6284853A (en) 1985-10-09 1985-10-09 Material for casting pattern

Publications (2)

Publication Number Publication Date
JPS6284853A true JPS6284853A (en) 1987-04-18
JPH0456699B2 JPH0456699B2 (en) 1992-09-09

Family

ID=16846959

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22655385A Granted JPS6284853A (en) 1985-10-09 1985-10-09 Material for casting pattern

Country Status (1)

Country Link
JP (1) JPS6284853A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006241256A (en) * 2005-03-02 2006-09-14 Kaneka Corp Expandable methyl methacrylate resin particle and foam obtained using the same
WO2017169568A1 (en) * 2016-03-30 2017-10-05 株式会社カネカ Process for producing expanded polyethylene-based resin beads and process for producing polyethylene-based molded resin object by in-mold foaming

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS49130460A (en) * 1973-04-17 1974-12-13
JPS5055675A (en) * 1973-09-18 1975-05-15
JPS5062267U (en) * 1973-10-11 1975-06-06
JPS50130866A (en) * 1974-04-04 1975-10-16
JPS53131227A (en) * 1977-04-22 1978-11-15 Hitachi Ltd Model for casting
JPS57165156A (en) * 1981-03-16 1982-10-12 Union Giken Kk Investment casting method

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS49130460A (en) * 1973-04-17 1974-12-13
JPS5055675A (en) * 1973-09-18 1975-05-15
JPS5062267U (en) * 1973-10-11 1975-06-06
JPS50130866A (en) * 1974-04-04 1975-10-16
JPS53131227A (en) * 1977-04-22 1978-11-15 Hitachi Ltd Model for casting
JPS57165156A (en) * 1981-03-16 1982-10-12 Union Giken Kk Investment casting method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006241256A (en) * 2005-03-02 2006-09-14 Kaneka Corp Expandable methyl methacrylate resin particle and foam obtained using the same
WO2017169568A1 (en) * 2016-03-30 2017-10-05 株式会社カネカ Process for producing expanded polyethylene-based resin beads and process for producing polyethylene-based molded resin object by in-mold foaming
JPWO2017169568A1 (en) * 2016-03-30 2019-02-07 株式会社カネカ Production method for polyethylene resin expanded particles, and method for producing expanded foam in polyethylene resin mold

Also Published As

Publication number Publication date
JPH0456699B2 (en) 1992-09-09

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