JPS61266146A - Master pattern material for casting - Google Patents

Master pattern material for casting

Info

Publication number
JPS61266146A
JPS61266146A JP10978585A JP10978585A JPS61266146A JP S61266146 A JPS61266146 A JP S61266146A JP 10978585 A JP10978585 A JP 10978585A JP 10978585 A JP10978585 A JP 10978585A JP S61266146 A JPS61266146 A JP S61266146A
Authority
JP
Japan
Prior art keywords
particles
casting
mold
crosslinked
resin
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
JP10978585A
Other languages
Japanese (ja)
Other versions
JPH0336613B2 (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 JP10978585A priority Critical patent/JPS61266146A/en
Publication of JPS61266146A publication Critical patent/JPS61266146A/en
Publication of JPH0336613B2 publication Critical patent/JPH0336613B2/ja
Granted legal-status Critical Current

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  • Molds, Cores, And Manufacturing Methods Thereof (AREA)

Abstract

PURPOSE:To form a master pattern for casting so as to have adequate workability and compressive strength and to provide a smooth surface having low water absorptivity thereto by putting the prefoamed particles of a crosslinked PP resin having a specific gel fraction into a mold and heating the same to expand to the specific density and average cell size. CONSTITUTION:Adequate amts. of water, antisticking agent talc, org. peroxide crosslinking agent such as 1,1-bis(t-butyl peroxy)3,3,5-trimethyl cyclohexane and crosslinking assistant divinyl benzene are added to the PP resin such as ethylene/propylene random copolymer having <=40% residue of n-heptane extraction and the mixture is heated in an autoclave to form the crosslinked resin particles. Suitable amts. of water and volatile org. foaming agent such as dichlorofluoromethane are added thereto and the particles are released after the pressurizing and heating up to form the prefoamed and crosslinked particles having 0.01-50% gel fraction. Such particles are put into a metallic mold and are heated to expand, then the foamed molding having 0.2-0.02g/cm<3> density and 70-1,000mum average cell size is obtd. The good master pattern for casting having the adequate cutting workability, compressive strength, smooth surface and low water absorptivity is thus obtd.

Description

【発明の詳細な説明】 〔技術分野〕 本発明は、架橋ポリプロピ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用原型材料に関し、さ
らに詳しくは、微細な気泡径とすぐれた表面硬度を有す
る架橋ポリプロピ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用原型材料に関するものである
[Detailed Description of the Invention] [Technical Field] The present invention relates to a molding material for casting that is mainly made of an in-mold foamed product of crosslinked polypropylene resin pre-expanded particles, and more specifically, it relates to a mold material for casting that is made mainly from an in-mold foamed product of cross-linked polypropylene resin pre-expanded particles. The present invention relates to a casting material whose main raw material is an in-mold foamed product of pre-expanded crosslinked polypropylene resin particles having surface hardness.

〔従来技術〕[Prior art]

従来から鋳造用原型材料としては木材が主材料として使
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、価
格が高いこと、乾燥が必要なこと、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、木材原型では重量
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。
Traditionally, wood has been used as the main material for casting molds, and even today, 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. It has drawbacks such as requiring skill, being inconvenient to transport as the wooden original is heavy, and if deformed during storage, it must be corrected each time it is used.

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用原型材料に用いる試
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。
Due to the above-mentioned drawbacks of wood, attempts have been made in recent years to use in-mold foam molded products of polystyrene as a casting material. 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、特定の方法で架橋発泡し
て得られたゲル分率30〜90%、カサ密度0.5−0
.05g/am3.平均気泡径が400μm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原型材
料が示されている。しかしながら、この鋳造用原型材料
は、発泡剤として熱分解型のアミド類を使用する為に精
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、その為に、砂との離型
性が悪く実際に使オ〕れていないのが現実である。
Japanese Patent Publication No. 47-43404 discloses a product which is crosslinked and foamed by a specific method and has a gel fraction of 30 to 90% and a bulk density of 0.5 to 0.
.. 05g/am3. A casting master material made of a crosslinked crystalline polyolefin resin foam having an average cell diameter of 400 μm or less is shown. However, since this casting material uses pyrolytic amides as a blowing agent, it cannot be used to produce precision castings, and it still has the disadvantage of high water absorption. The reality is that it has poor releasability from sand and is not actually used.

〔目   的〕〔the purpose〕

本発明は、従来のU進用発泡体原型材料に見られる前記
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
の小さな鋳造用発泡体原型材料を提供することを目的と
する。
An object of the present invention is to provide a foam molding material for casting that overcomes the above-mentioned drawbacks found in conventional foam molding materials for U-adjustment and has a low water absorption rate and provides castings with good one-dimensional accuracy.

〔構  成〕 本発明は、ゲル分率0.旧〜50%の架橋ポリプロピレ
ン系樹脂予備発泡粒子を型内にて一体に成形した密度0
.2〜0.02g/co?、平均気泡径70−1000
 μmの架橋ポリプロピレン系樹脂型内発泡成形体よす
なる鋳造用原型材料を要旨とする。
[Configuration] The present invention has a gel fraction of 0. Density 0 made by integrally molding 50% cross-linked polypropylene resin pre-expanded particles in a mold
.. 2~0.02g/co? , average bubble diameter 70-1000
The gist of this article is a molding material for casting, which is a cross-linked polypropylene resin in-mold foamed molded product having a micrometer diameter.

本発明の鋳造用原型は、ゲル分率が0.01〜50%の
架橋ポリプロピ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 mold of the present invention is made of a foam formed by foam-molding crosslinked polypropylene resin pre-expanded particles having a gel fraction of 0.01 to 50% in a mold. In this case, the gel fraction 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 (%)=−X100 Pニゲル分率(%) ■、: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、又吸水率も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、前記0.
01〜50%、好ましくは5〜45%に規定するのがよ
い。
P (%) = -X100 P gel fraction (%) ■: Weight of cross-linked pre-expanded particles M: Weight of insoluble matter When the gel fraction exceeds 50%, void formation increases in the molded product. In addition, the water absorption rate also increases, which is not preferable, and the gel fraction of the crosslinked resin pre-expanded particles is set to the above-mentioned 0.
It is preferable to set the range to 0.01 to 50%, preferably 5 to 45%.

また、本発明で鋳造用原型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0.02〜0.2g/cm3.好ましくは0.03
〜0.15g/cm’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80〜900
μm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、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JTS K−6767)は、一般
的には、0.7kg/al以−Fに規定するのがよい。
Further, in the in-mold foamed product of the pre-expanded particles used as a casting material in the present invention, the density (bulk density) is 0.02 to 0.2 g/cm3. Preferably 0.03
~0.15 g/cm', and the average bubble diameter is 70 to 1000 μm, preferably 80 to 900 μm.
It is defined in the μm range. 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 this method 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 (JTS K-6767) of the foam is generally preferably set to 0.7 kg/al or more -F.

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。
In addition, 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.

本発明の鋳造用原型素材樹脂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−プロピレンブロー4= ツク共重合体、プロピレンi1を独重合体、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、エチレン含有鼠0.5重量%
〜10重駄%、好ましくは11%〜5重量%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。また
、ポリプロピレン系樹脂は、40%以下のn−へブタン
抽出残渣割合を示すものの使用が剛性ある発泡体を得る
にから好ましい。この場合、n−ヘプタン抽出残渣割合
は、立体規則性を意味し、次の式で表わされる。
The polypropylene resins used as the mold material resin for casting of the present invention include ethylene-propylene random copolymer, ethylene-propylene blow 4=tsuk copolymer, propylene i1 homopolymer, and propylene-1-butene random copolymer. Examples include merging. In particular, among these polymers, 0.5% by weight of ethylene
Preference is given to using an ethylene-propylene random copolymer of up to 10% by weight, preferably between 11% and 5% by weight. Further, it is preferable to use a polypropylene resin having an n-hebutane extraction residue ratio of 40% or less because a rigid foam can be obtained. In this case, the n-heptane extraction residue ratio means stereoregularity and is expressed by the following formula.

■、 R(%)=−X100 Ran−ヘプタン抽出残渣割合(%) L:n−へブタン8時間抽出後の不溶分の重量M:n−
へブタン抽出前の重量 本発明において、前記のポリプロピレン系樹脂はそれぞ
れ単独でも用いられる他、複数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。
■, R (%) = -X100 Ran-heptane extraction residue ratio (%) L: Weight of insoluble matter after 8 hours of n-heptane extraction M: n-
Weight before hebutane extraction In the present invention, the above-mentioned polypropylene resins may be used alone or in combination, and in the case of a blend, the blending ratio is arbitrary.

本発明の鋳造用原型材料は、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いわゆる架橋予
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。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(し−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(1,−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が好ましい。前記
架橋剤の使用量は、樹脂100重欧部に対し、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、0.05〜5重址部の割
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
。この場合、融着防止剤しては、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。
The molding material for casting of the present invention is an in-mold crosslinked foam molded product formed from so-called crosslinked pre-expanded particles formed by crosslinking the resin particles and foaming the obtained crosslinked particles. In this case, 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 increasing the temperature to the crosslinking temperature. It can be obtained by raising and holding the temperature at . Examples of the crosslinking include dicumyl peroxide, 1,1-bis(butylperoxy)3,3.5
-trimethylcyclohexane, n-butyl-4,4-bis(1,-butylperoxy)valerate, thi-butylcumyl peroxide, 2,5-dimethyl-2,5-di(thi-butylperoxy)hexane, etc. of organic peroxides are used. Further, it is preferable to use divinylbenzene as a crosslinking aid in combination with these crosslinking agents. The amount of the crosslinking agent used is 0.05 parts per 100 parts of resin.
The amount of divinylbenzene used is 0.05 to 5 parts by weight per 100 parts by weight of the resin. 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. 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
容器中で空気で加圧し、粒子内に0.5〜3kg/cJ
G程度の粒子内圧を持たせた後、成形用金型内に入れ、
加熱発泡により、一体に成形し、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, and 0.5 to 3 kg/cJ is added into the particles.
After giving the particles an internal pressure of about G, put them into a mold for molding,
By heating and foaming, the product is integrally molded into a 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、鋳造用原型材料として使用する。
The crosslinked polyethylene resin in-mold foamed molded product thus obtained is dried and used as a mold material for casting.

〔効  果〕〔effect〕

本発明の鋳造用原型材料は、前記した特定の発泡体から
なるもので、従来の木材や、発泡体からなるものと同様
に使用されるが、本発明で用いる発泡体は、す1断加圧
性にすぐれるため、従来の木型模型製製造する場合に用
いた1−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材料を与える。また、本発明の鋳
造用原型材料は、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 mold material for casting of the present invention is made of the above-mentioned specific foam and can be used in the same way as conventional materials made of wood or foam. Because of its excellent compressibility, it has the advantage that the tools used in conventional wooden model manufacturing can be used as is, and it also has a smooth surface and high compression hardness, and is even more advantageous.
Since it has extremely low water absorption, it provides a casting material with excellent dimensional stability. Further, the casting mold 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.

実施例1〜5、比較例1〜5 オートクレーブに第1表に示すエチレン−プロピレンラ
ンダム共重合体粒子100重量部、水300重景部、融
着防止剤として微粒状の酸化アルミニウム0.3重斌部
、第1表に示す架橋剤及び架橋助剤を配合し、攪拌しな
がら100℃に昇温し、この温度に1時間保持した。そ
の後、150°Cに昇温し1時間保持し架橋反応を行っ
た後、容器をいったん冷却し、架橋樹脂粒子を取り出し
た。
Examples 1 to 5, Comparative Examples 1 to 5 In an autoclave, 100 parts by weight of the ethylene-propylene random copolymer particles shown in Table 1, 300 parts by weight of water, and 0.3 parts by weight of finely divided aluminum oxide as an anti-fusing agent were added. A crosslinking agent and a crosslinking aid shown in Table 1 were blended, the temperature was raised to 100° C. while stirring, and the temperature was maintained for 1 hour. Thereafter, the temperature was raised to 150°C and held for 1 hour 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重址部、発泡剤として第1表に示す揮発
性発泡剤を配合し、攪拌しながら第1表に示す発泡温度
に昇温し、この温度で15分間保持した後、容器内を空
気で40kg/cl#G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, 100 parts by weight of the crosslinked resin particles, 300 parts by weight of water, and a volatile blowing agent shown in Table 1 as a blowing agent were added to the autoclave again, and the temperature was raised to the foaming temperature shown in Table 1 while stirring. After holding at this temperature for 15 minutes, one end of the container was opened while pressurizing the inside of the container to 40 kg/cl #G, and the crosslinked particles and water were released under atmospheric pressure to perform foaming and pre-foaming. Crosslinked particles were obtained.

次に、この予備発泡架橋粒子を耐圧容器に入れ、空気に
て加圧し、予備発泡架橋粒子内に、1.5kg/DIt
G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/ c+# Gの蒸気圧にて加熱発泡さ
せた後、冷却し、粒子が融着した発泡成形体、すなわち
鋳造用原型材料を得た。
Next, the pre-expanded cross-linked particles were placed in a pressure-resistant container and pressurized with air, so that 1.5 kg/DIt was added to the pre-expanded cross-linked particles.
The particle had an internal pressure of G. The particles were placed in a mold, heated and foamed at a steam pressure of 3.2 kg/c+#G, and then cooled to obtain a foamed molded article in which the particles were fused, that is, a casting material.

次に、前記で得られた各型内発泡成形体について、その
切断加工の難易度、切断品の表面状態、圧縮カタサ、及
び吸水率をそれぞれ下記に示す基準で評価し、その結果
を第1表に示す。
Next, each of the in-mold foam molded products obtained above was evaluated in terms of the difficulty of cutting, the surface condition of the cut product, the compression roughness, and the water absorption rate, and the results were evaluated using the following criteria. Shown in the table.

なお、切断加工難易度は、型内発泡成形体をハンドソー
により厚さ10mmに切断加工を行い、その際の切断加
工の難易で評価し、また切断品の表面状態は、その際に
得られる切断品の表面状態を目視観察により評価した。
The difficulty of cutting is evaluated by cutting the in-mold foam molded product into a thickness of 10 mm using a hand saw, and the surface condition of the cut product is evaluated by the difficulty of cutting at that time. The surface condition of the product was evaluated by visual observation.

〔評価基準〕〔Evaluation criteria〕

(1)切断加工の難易度: O・・・切断時に抵抗がなくスムースに切断できる。 (1) Difficulty of cutting process: O: 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.

×・・・切断時に抵抗が大きく振動を発生する。×...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.

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

×・・・表面が荒れかつもげる粒子がある。×: Some particles have rough and peeling surfaces.

(3)圧縮カタサ(、TTS−に−6767に準拠):
O・・・0.7kg/cJ以上 Δ・・−0,7kg/crl−0,4J/cIIT×・
・・0.4kg/cJ以下 (4)吸水率(JIS−に−6767B法):0−0.
003g/cn?未満 Δ・・・0.03〜0.003g/rJ×・・・0.0
3g/cJ以上 18開昭Gl−266146(5) 18開BHGI−266146(6) #  −S く甚    粂q 奪  長  凝 1   聾 °り一 1      堰 に 八 Δ     犯 も べ      ÷ 符     管 =      殊 <     ベ 置 五      胃 塊 雲     ピ
(3) Compression Katasa (compliant with TTS-6767):
O...0.7kg/cJ or more Δ...-0.7kg/crl-0.4J/cIIT×・
・・0.4 kg/cJ or less (4) Water absorption rate (JIS-6767B method): 0-0.
003g/cn? Less than Δ...0.03 to 0.003g/rJ×...0.0
3 g/cJ or more 18 Kaisho Gl-266146 (5) 18 Kai BHGI-266146 (6) beokigogo gastric mass cloud pi

Claims (2)

【特許請求の範囲】[Claims] (1)ゲル分率が0.01〜50%の架橋ポリプロピレ
ン系樹脂予備発泡粒子を型内にて一体に成形した密度0
.2〜0.02g/cm^3、平均気泡径70〜100
0μmの架橋ポリプロピレン系樹脂型内発泡成形体より
なる鋳造用原型材料。
(1) Pre-expanded crosslinked polypropylene resin particles with a gel fraction of 0.01 to 50% are integrally molded in a mold with a density of 0.
.. 2~0.02g/cm^3, average bubble diameter 70~100
A molding material for casting consisting of a 0μm crosslinked polypropylene resin in-mold foam molding.
(2)架橋ポリプロピレン系樹脂予備発泡粒子が、揮発
性発泡剤を使用して得られたものである特許請求の範囲
第1項記載の鋳造用原型材料。
(2) The mold material for casting according to claim 1, wherein the pre-expanded crosslinked polypropylene resin particles are obtained using a volatile blowing agent.
JP10978585A 1985-05-22 1985-05-22 Master pattern material for casting Granted JPS61266146A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10978585A JPS61266146A (en) 1985-05-22 1985-05-22 Master pattern material for casting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10978585A JPS61266146A (en) 1985-05-22 1985-05-22 Master pattern material for casting

Publications (2)

Publication Number Publication Date
JPS61266146A true JPS61266146A (en) 1986-11-25
JPH0336613B2 JPH0336613B2 (en) 1991-06-03

Family

ID=14519156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10978585A Granted JPS61266146A (en) 1985-05-22 1985-05-22 Master pattern material for casting

Country Status (1)

Country Link
JP (1) JPS61266146A (en)

Also Published As

Publication number Publication date
JPH0336613B2 (en) 1991-06-03

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