JPS58118833A - Preparation of reprocessed synthetic resin foam - Google Patents

Preparation of reprocessed synthetic resin foam

Info

Publication number
JPS58118833A
JPS58118833A JP155482A JP155482A JPS58118833A JP S58118833 A JPS58118833 A JP S58118833A JP 155482 A JP155482 A JP 155482A JP 155482 A JP155482 A JP 155482A JP S58118833 A JPS58118833 A JP S58118833A
Authority
JP
Japan
Prior art keywords
mold
raw material
foam
parts
resin foam
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP155482A
Other languages
Japanese (ja)
Inventor
Sadao Kumasaka
貞男 熊坂
Satomi Tada
多田 郷見
Shigeo Horikoshi
堀越 成夫
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.)
Toyo Quality One Corp
Original Assignee
Toyo Rubber Chemical Industrial 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 Toyo Rubber Chemical Industrial Co Ltd filed Critical Toyo Rubber Chemical Industrial Co Ltd
Priority to JP155482A priority Critical patent/JPS58118833A/en
Publication of JPS58118833A publication Critical patent/JPS58118833A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To prepare a reprocessed resin foam with low cost from a scrap of ethylene/vinyl acetate copolymer resin foam, by a method wherein a crosslinker and a foaming agent are added to fragments of a resin foam crushed within a kneader, and the mixt. is introduced into a mold and heated. CONSTITUTION:Scraps and rejects of ethylen/vinyl acetate copolymer resin foam (those with low density are preferred) are kneaded and crushed by a kneader such as roller, to form a viscous resin material. Then, 100pts.wt. above resin material, 0.5-5pts.wt. crosslinker (e.g., dicumyl peroxide), and 3-10pts.wt. foaming agent (e.g., azodicarbonamide) are kneaded to give a compd. After filled and closed into a mold, the compd. is crosslinked and foamed with heat to yield a high density reprocessed synthetic resin foam on removing from the mold. In the above method, when the amt. of a foaming agent is 10-50pts.wt. and the removing temp. from the mold is 50-80 deg.C lower than the heating temp. after crosslinking and foaming, a low-density foamed product can be obtained.

Description

【発明の詳細な説明】 本発明は再生合成樹脂発泡体の製造方法に関し、特に、
エチレン−酢酸ビニル共重合樹脂発泡体の裁断片や不良
品を原料として嵩密度または低密度の再生合成樹脂発泡
体を製造する方法に係る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing recycled synthetic resin foam, and in particular,
The present invention relates to a method for producing a recycled synthetic resin foam having a bulk density or a low density using shredded pieces or defective products of an ethylene-vinyl acetate copolymer resin foam as a raw material.

合成樹脂発泡体は建材、クッシ冒ン材等の産業資材とし
て極めて広範な用途に使用されている。これら合成樹脂
発泡体では所定寸法に裁断する際に生じた裁断片や不良
品等、用途がなくてそのまま廃棄されるものがかなりの
量にのぼる。しかも、これらは産業廃棄物として焼却等
により処理しなければならず、そのための費用およびこ
れによる公害等、大きな問題となっている0このため、
省資渾、コスト低減および分書防止等の観点から、これ
ら合成樹脂発泡体の廃棄物を原料として、これを新たな
合成樹脂発泡体に再生する方途が強く要望されている。
Synthetic resin foams are used in an extremely wide range of applications as industrial materials such as building materials and cushioning materials. A considerable amount of these synthetic resin foams have no use and are discarded as they are, such as fragments and defective products that are generated when they are cut into predetermined dimensions. Moreover, these must be disposed of as industrial waste by incineration, etc., which poses a major problem due to the cost and pollution caused by this process.
From the viewpoints of resource saving, cost reduction, and prevention of separate documents, there is a strong demand for a method of recycling these synthetic resin foam wastes into new synthetic resin foams as raw materials.

本願の発明者等はこのような事情に鑑み、合成樹脂発泡
体の廃棄物から再生合成樹脂発泡体を製造する方法につ
いて鋭意研究を重ねた結果、今回、エチレン−酢酸ビニ
ル共重合樹脂(以下EVAという)の発泡体について上
記再生合成樹脂発泡体の製造方法を見出したものである
In view of these circumstances, the inventors of the present application have conducted intensive research on a method for producing recycled synthetic resin foam from waste synthetic resin foam, and as a result, they have developed an ethylene-vinyl acetate copolymer resin (hereinafter referred to as EVA). We have discovered a method for producing the above-mentioned recycled synthetic resin foam.

即ち、本願の第1発明は、EvA発泡体片をロール等の
混線機で圧壊することにより樹脂原料とし、該樹脂原料
100重量部に対して架橋剤05〜5.0重量部および
発泡剤3〜10重量部を添加混練したコンIIウンド原
料を成形製内に充填して被蓋で強固に閉塞し、ついで前
記充填原料を型内に充填したtまで加熱することにより
発泡および架橋反応を生じせしめた後、成形型の被蓋を
開放して一挙に最終発泡体を得ることを特徴とする高密
度再生合成樹脂発泡体の製造方法である。
That is, in the first invention of the present application, a resin raw material is obtained by crushing EvA foam pieces with a mixer such as a roll, and 05 to 5.0 parts by weight of a crosslinking agent and 3 parts by weight of a blowing agent are added to 100 parts by weight of the resin raw material. ~10 parts by weight of the compound II powder raw material added and kneaded is filled into a molded mold and tightly closed with a cover, and then the filled raw material is heated to the temperature at which it is filled into the mold to cause foaming and crosslinking reactions. This is a method for producing a high-density recycled synthetic resin foam, which is characterized in that after the molding process is completed, the lid of the mold is opened to obtain the final foam all at once.

また、本願の第2発明は、EVA発泡体片をロール等の
混練機で圧壊することにより樹脂原料とし、該樹脂原料
100重量部に対して架橋剤05〜5.0重量部および
発泡剤10〜50重量部を添加混練し念コンノやランド
原料を成形型内に充填して被蓋で強固に閉塞し、ついで
前記充填原料を畿内に充填したままで加熱することによ
り発泡剤を分解させ、次に前記充填原料を型内に保持し
九ままで前記加熱温度よりも50〜80℃低い温度にま
で冷却し、その後成形型の被蓋を開放して一挙に最終発
泡体を得ることを特徴とする低密度再生合成樹脂発泡体
の製造方法である。
Further, in the second invention of the present application, a resin raw material is obtained by crushing EVA foam pieces with a kneader such as a roll, and 05 to 5.0 parts by weight of a crosslinking agent and 10 parts by weight of a blowing agent are added to 100 parts by weight of the resin raw material. ~50 parts by weight is added and kneaded, and the mold is filled with the nenkonno or land raw material, which is tightly closed with a cover, and then the foaming agent is decomposed by heating while the filling raw material is filled in the mold, Next, the filling material is held in the mold and cooled to a temperature 50 to 80 degrees Celsius lower than the heating temperature, and then the cover of the mold is opened to obtain the final foam at once. This is a method for producing a low-density recycled synthetic resin foam.

次に、この二つの発明の詳細な説明する。Next, these two inventions will be explained in detail.

本発明において用いるEVA発泡体片としては、従来の
製造方法で製造された高密度ま九は低密度のEVA発泡
体を用いることができる。このEvAlllfliは任
意でよいが、通常はエチレン100部に対して酢酸ビニ
ル10〜40のものが用いられる。これらのEVA発泡
体片を通常の混線機で圧壊して練ると、粘性を帯びた樹
脂原料が得られる。この場合、EVA発泡体片は全て使
用可能であるが望ましくは特願昭54−65843号の
方法で得られた低密度EVA発泡体片を用いるのがよい
As the EVA foam piece used in the present invention, a high-density or low-density EVA foam manufactured by a conventional manufacturing method can be used. This EvAllfli may be arbitrary, but it is usually 10 to 40 parts of vinyl acetate per 100 parts of ethylene. When these EVA foam pieces are crushed and kneaded using a common mixer, a viscous resin raw material is obtained. In this case, any EVA foam piece can be used, but it is preferable to use a low-density EVA foam piece obtained by the method disclosed in Japanese Patent Application No. 54-65843.

本発明に用いる架橋剤は、例えば、ジクミル/9−オキ
サイド、2,5−ジメチル−2,5−ノ(t−ブチル)
ノや一オキサイド、1.3−ビス(t−プチルノ9−オ
キシイソプロピル)ベンゼン、m−オクタデシルアジド
ホルメート、t−ブチルパーオキシクメン等の有機過酸
化物である。
Examples of the crosslinking agent used in the present invention include dicumyl/9-oxide, 2,5-dimethyl-2,5-no(t-butyl)
These are organic peroxides such as monooxide, 1,3-bis(t-butylno-9-oxyisopropyl)benzene, m-octadecylazidoformate, and t-butylperoxycumene.

この架橋剤の添加量は発泡剤の使用量とも関連するが、
EVA発泡体を圧壊して得喪樹wr原料100重量部に
対して0.5〜5.0重量部である。これが0.5重量
部に満た表いと架橋が充分に行なわれず、また5、0重
量部を越えると発泡剤とのバランスが失なわれて不安定
な発泡が行なわれる。
The amount of crosslinking agent added is also related to the amount of blowing agent used,
The amount is 0.5 to 5.0 parts by weight per 100 parts by weight of the raw material obtained by crushing the EVA foam. If the amount is less than 0.5 parts by weight, sufficient crosslinking will not occur, and if it exceeds 5.0 parts by weight, the balance with the foaming agent will be lost and unstable foaming will occur.

本発明における発泡剤としては、例えば、アゾジカーゲ
ンアミド、ジニトロソペンタメチレンテトラミン、p−
)ルエンスルホニルヒドラジン、アゾビスイソブチロニ
トリル、ジアゾアミノアソベンゼン、トルエンスルホニ
ルセミカルバジドを用いることができる。これら発泡剤
の使用量は、第1発明ではEVA発泡体片を圧壊して得
た樹脂、原料100重量部に対して3〜10重量部であ
るが、他方、第2発明では10〜50重量部である“。
Examples of the blowing agent in the present invention include azodicagenamide, dinitrosopentamethylenetetramine, p-
) Luenesulfonylhydrazine, azobisisobutyronitrile, diazoaminoisobenzene, toluenesulfonyl semicarbazide can be used. In the first invention, the amount of these blowing agents used is 3 to 10 parts by weight based on 100 parts by weight of the resin and raw material obtained by crushing EVA foam pieces, while in the second invention, it is 10 to 50 parts by weight. Department “.

このように第1発明と第2発明で発泡剤の使用量が異な
るのは、第1発明が密度0605〜0.3の、高密度発
泡体を得るものであるのに対して、第2発明は密度0.
02〜0.05の低密度発泡体を得るものであるからで
ある。
The reason why the amount of blowing agent used is different between the first invention and the second invention is that the first invention obtains a high-density foam with a density of 0605 to 0.3, whereas the second invention has a density of 0.
This is because a low density foam with a density of 0.02 to 0.05 is obtained.

本発明においては、必要に応じて発泡助剤、着色剤、充
填材等、上記以外の添加剤を用いる。
In the present invention, additives other than those mentioned above, such as foaming aids, colorants, fillers, etc., are used as necessary.

他の樹脂を充填材として用いる場合には、主原料との相
溶性からポリエチレン、ポリスチレン等のポリオレフィ
ン系樹脂を用い、その添加量は30チ以下とする。また
、15チ以下の合成ゴムまたは天然ゴムを添加すると、
これが所謂つなぎの作用をしてロールによる加工の場合
などは加工性が良好となり、シート状になり易くなる。
When using another resin as a filler, a polyolefin resin such as polyethylene or polystyrene is used because of its compatibility with the main raw material, and the amount added is 30 inches or less. Also, if 15 inches or less of synthetic rubber or natural rubber is added,
This acts as a so-called binder, and when processed by rolls, the processability is good and it becomes easy to form a sheet.

本発明においては上記混合料量を充分混練した後、これ
を成形型の中に充填する。ここに用いる成形型は任意の
形でよいが、発泡成型品の脱型に当って製品が一挙に型
内から飛び出すので、上広形の開口部を有するものがよ
い。発泡原料は成形型に略充満するか、ややこれを押圧
するようにして充填してから、型罠被蓋をしてこれを強
固に閉塞固定する。被蓋の固定方法は任意でよいが、臘
蓋の開閉を自在にでき、しがも閉型を強固に行なうのに
便利な方法は、プレス機を用いその先端に型の被蓋を装
着し、これで型の開閉を行なう方法である。
In the present invention, after the above amount of the mixture is sufficiently kneaded, it is filled into a mold. The mold used here may be of any shape, but it is preferable that the mold has a wide opening at the top, since the product will jump out of the mold all at once when the foamed product is demolded. The foaming raw material is filled into the mold by substantially filling it or pressing it slightly, and then the mold trap is covered and the mold is tightly closed and fixed. The cover can be fixed in any way you like, but a convenient way to open and close the cover freely and to securely close the cover is to attach a mold cover to the tip using a press. , this is how to open and close the mold.

こうして準備が完了したら発泡作業を行なうが、この発
泡工程は第1発明と第2発明とで若干相違している。ま
ず第1発明の場合は、通常の樹脂発泡体の製造と同様、
成形型に充填したままで加熱することにより発泡および
架橋反応を生じせしめた後、成形型の被蓋を開放して一
挙に最終発泡体を得る。このときの加熱温度は使用した
発泡剤の分解温度にもよるが、大体160〜170℃前
後である。
When the preparations are completed in this way, a foaming operation is carried out, but this foaming process is slightly different between the first invention and the second invention. First, in the case of the first invention, as in the production of ordinary resin foam,
After foaming and crosslinking reactions are caused by heating the mixture while it is filled in the mold, the lid of the mold is opened to obtain the final foam at once. The heating temperature at this time depends on the decomposition temperature of the blowing agent used, but is generally around 160 to 170°C.

これに対して、第2発明の場合はwc1発明と同様の温
度で加熱して発泡剤を充分に分解した後、これをそのま
ま一度冷却する。このときの冷却温度は使用原料、添加
剤の種類および量その他によって定められるもので、−
律に定めることはできないが、大体加熱時の温度よりも
50〜80℃程度低い60〜110℃とする。この冷却
は強制冷却として、例えば成形型のノヤケ、ットに冷却
水を送るなどして行なう。この冷却の後、成形型の被蓋
を開放して一挙に最終発泡体を得る。このように、加熱
した後に一度冷却を行なうのは、第2発明が密度0.0
2〜0.05の低密度発泡体を得るものであることに起
因する亀ので、次の理由によるものである。
On the other hand, in the case of the second invention, the foaming agent is sufficiently decomposed by heating at the same temperature as in the wc1 invention, and then the product is cooled as it is. The cooling temperature at this time is determined by the raw materials used, the type and amount of additives, etc.
Although it cannot be determined by law, the temperature is generally 60 to 110°C, which is about 50 to 80°C lower than the temperature during heating. This cooling is performed as forced cooling, for example, by sending cooling water to the nozzle of the mold. After this cooling, the lid of the mold is opened and the final foam is obtained all at once. In this way, cooling once after heating is the second invention with a density of 0.0.
This is due to the following reasons: 2 to 0.05% low density foam is obtained.

即ち、第2発明では低密度発泡体を得る九めに第1発明
よりも多量の発泡剤を使用しており、この場合にもし第
1発明と同様の発泡工程で発泡させようとすると、加熱
された成形屋内での発泡圧が異常に高圧となり、脱型の
際この高圧により気泡体が炸裂して飛散してしまい、所
望の発泡体が得られないからである。これに対して、本
願第2発明では成形型内で発泡剤が分解した生成したガ
スの蒸気圧が冷却による温度低下と共に減少し、内圧が
低下するものと考えられる。この結果、冷却した後に成
形型を解放すると、気泡体の飛散を伴うことなく一挙に
発泡が行なわれ、低密度発泡体が得られる。
That is, in the second invention, a larger amount of blowing agent is used than in the first invention to obtain a low-density foam, and in this case, if foaming is attempted in the same foaming process as in the first invention, heating This is because the foaming pressure in the molding room becomes abnormally high, and when demolding, the foam explodes and scatters due to this high pressure, making it impossible to obtain the desired foam. On the other hand, in the second invention of the present application, it is considered that the vapor pressure of the gas generated by decomposing the blowing agent in the mold decreases as the temperature decreases due to cooling, and the internal pressure decreases. As a result, when the mold is released after cooling, foaming occurs all at once without scattering of air bubbles, resulting in a low-density foam.

上述した本発明によれば、従来は廃棄処分されていたE
VA発泡体の載断片や不良品を原料に用い、これを高書
度あるいは低密度の新たな合成樹脂発泡体に再生するこ
とができ、従って、省資源、公害防止およびコスト低減
に大きく寄与するものである。また、本発明によシ得ら
れる再生合成樹wr発泡体は、下記実施例にも示される
ように、従来製造されているEVA発泡体と略同等の物
性を有している。
According to the present invention described above, E
It is possible to use the loaded pieces and defective products of VA foam as raw materials and recycle them into new synthetic resin foams with high density or low density, thus greatly contributing to resource saving, pollution prevention, and cost reduction. It is something. Furthermore, the recycled synthetic resin foam obtained by the present invention has approximately the same physical properties as the conventionally produced EVA foam, as shown in the examples below.

以下に本発明の詳細な説明する。The present invention will be explained in detail below.

実施例1 比重0071のEVA発泡体をオープンロールにて圧壊
し友もの100重量部に対し、発泡剤AK”27.5重
量部、架橋剤パーオキサイド0.75重量部、イソグレ
ンゴム15重量部を混練したものをプレス加圧下にて1
58℃で20分間加熱し、発泡成形させ、比重O1目j
VdのEVA発泡体を得た・実施例2 比重0071のEVA発泡体をオープンロールにて圧壊
したもの100重量部に対し、発泡剤AKφ212重量
部、架橋剤1.1重量部、イソグレンゴム15重量部を
混練したものをプレス加圧下にて158℃で20分間加
熱后、発泡、成形して比重0.0721r/aiのEV
A発泡体を得た。
Example 1 An EVA foam with a specific gravity of 0071 was crushed with an open roll, and 27.5 parts by weight of the blowing agent AK, 0.75 parts by weight of crosslinking agent peroxide, and 15 parts by weight of isogrene rubber were kneaded with 100 parts by weight of the foam. 1 under pressure in a press
Heated at 58℃ for 20 minutes, foamed and molded to specific gravity O1
Obtained EVA foam with Vd Example 2 100 parts by weight of EVA foam with specific gravity 0071 crushed with an open roll, 212 parts by weight of blowing agent AKφ, 1.1 parts by weight of crosslinking agent, 15 parts by weight of isogrene rubber. The mixture was heated under press pressure at 158°C for 20 minutes, then foamed and molded to form an EV with a specific gravity of 0.0721r/ai.
Foam A was obtained.

実施例3 圧壊物100phr、、EVA樹脂7.5phr、、発
泡剤7.5phr、、架橋剤0.75 p h r、に
てIB8℃×20分で比重0.1141r/−を得た。
Example 3 A specific gravity of 0.1141 r/- was obtained at IB 8° C. for 20 minutes using 100 phr of crushed material, 7.5 phr of EVA resin, 7.5 phr of foaming agent, and 0.75 phr of crosslinking agent.

Claims (2)

【特許請求の範囲】[Claims] (1)  エチレン酢酸ビニル共重合樹脂発泡体片をロ
ール等の混線機で圧壊することにより樹脂原料とし、該
樹脂原料100重量部に対して架橋剤0,5.〜5.0
重量部および発泡剤3〜10重量部を添加混練したコン
パウンド原料を成形型内に′充填して被蓋で強固に閉塞
し、ついで前記充填原料を型内圧充填したままで加熱す
ることにより発泡および架橋反応を生じせしめた後、成
形型の被蓋を開放して一挙に最終発泡体を得ることを特
徴とする養令妾再生合成樹脂発泡体の製造方法。
(1) A resin raw material is obtained by crushing ethylene vinyl acetate copolymer resin foam pieces with a mixer such as a roll, and 0.5 parts of a crosslinking agent is added to 100 parts by weight of the resin raw material. ~5.0
A compound raw material prepared by adding and kneading 3 to 10 parts by weight of a blowing agent and a foaming agent is filled into a mold, tightly closed with a cover, and then heated while the filled raw material is filled with the mold's internal pressure to cause foaming and 1. A method for producing a recycled synthetic resin foam, which is characterized in that after a crosslinking reaction occurs, the lid of a mold is opened to obtain a final foam all at once.
(2)  エチレン酢酸ビニル共重合樹脂発泡体片をロ
ール等の混線機で圧壊することにより樹脂原料とし、該
樹脂原料100重量部に対して架橋剤05〜50重量部
および発泡剤10〜50重量部を添加混練したコンパウ
ンド原料を成形型内に充填して被蓋で強固に閉塞し、つ
いで前記充填原料を盤内に充填したままで加熱すること
により発泡剤を分解させ、次に前記充填原料を型内に保
持したままで前記加熱温度よりも50〜80℃低い温度
にまで冷却し、その後成形減の被蓋を開放して一挙に最
終発泡体を得ることを特徴とする會賽債再生合戊樹脂発
泡体の製造方法0
(2) A resin raw material is obtained by crushing ethylene vinyl acetate copolymer resin foam pieces with a mixer such as a roll, and 05 to 50 parts by weight of a crosslinking agent and 10 to 50 parts by weight of a blowing agent are prepared for 100 parts by weight of the resin raw material. The compound raw material added and kneaded is filled into the mold and tightly closed with a cover, and then the foaming agent is decomposed by heating the filled raw material while it is filled in the disk. A method of recycling a merchandising bond, which is characterized in that the foam is cooled to a temperature 50 to 80°C lower than the heating temperature while it is held in the mold, and then the molding cover is opened to obtain the final foam at once. Manufacturing method of synthetic resin foam 0
JP155482A 1982-01-08 1982-01-08 Preparation of reprocessed synthetic resin foam Pending JPS58118833A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP155482A JPS58118833A (en) 1982-01-08 1982-01-08 Preparation of reprocessed synthetic resin foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP155482A JPS58118833A (en) 1982-01-08 1982-01-08 Preparation of reprocessed synthetic resin foam

Publications (1)

Publication Number Publication Date
JPS58118833A true JPS58118833A (en) 1983-07-15

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP155482A Pending JPS58118833A (en) 1982-01-08 1982-01-08 Preparation of reprocessed synthetic resin foam

Country Status (1)

Country Link
JP (1) JPS58118833A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100408704B1 (en) * 2001-03-05 2003-12-06 문성철 A composition of foams with waste materials and ground tire rubber and foams thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54129061A (en) * 1978-03-17 1979-10-06 Dynamit Nobel Ag Production of polyolefin based plastic foam
JPS55157629A (en) * 1979-05-28 1980-12-08 Toyo Rubber Chem Ind Co Ltd Foam of low-density ethylenevinyl acetate copolymer resin and its preparation

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54129061A (en) * 1978-03-17 1979-10-06 Dynamit Nobel Ag Production of polyolefin based plastic foam
JPS55157629A (en) * 1979-05-28 1980-12-08 Toyo Rubber Chem Ind Co Ltd Foam of low-density ethylenevinyl acetate copolymer resin and its preparation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100408704B1 (en) * 2001-03-05 2003-12-06 문성철 A composition of foams with waste materials and ground tire rubber and foams thereof

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