JPH0813494B2 - Method for producing foamed molded article - Google Patents
Method for producing foamed molded articleInfo
- Publication number
- JPH0813494B2 JPH0813494B2 JP62089940A JP8994087A JPH0813494B2 JP H0813494 B2 JPH0813494 B2 JP H0813494B2 JP 62089940 A JP62089940 A JP 62089940A JP 8994087 A JP8994087 A JP 8994087A JP H0813494 B2 JPH0813494 B2 JP H0813494B2
- Authority
- JP
- Japan
- Prior art keywords
- melt
- foaming
- impact
- mold
- extruded
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
- B29C48/375—Plasticisers, homogenisers or feeders comprising two or more stages
- B29C48/388—Plasticisers, homogenisers or feeders comprising two or more stages using a screw extruder and a ram or piston
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Molding Of Porous Articles (AREA)
Description
【発明の詳細な説明】 〔技術分野〕 本発明は、熱可塑性樹脂を原料とする発泡成形体の製
造方法に関するものである。Description: TECHNICAL FIELD The present invention relates to a method for producing a foamed molded article using a thermoplastic resin as a raw material.
従来、金型を使用して発泡熱可塑性樹脂成形品を製造
する方法としては、いわゆるビーズ成形法と発泡射出成
形法が代表的なものである。しかしながら、ビーズ成形
法は原料樹脂粒子を予備発泡させて得られたビーズを金
型内で加熱して2次発泡させながら融着させて成形する
という2段の発泡工程を含むため、操作が煩雑であるば
かりでなく、成形品にビーズ形状や蒸気孔の跡が残り、
外観不良を呈するという欠点がある。更にビーズ成形法
において、特にポリオレフィン系樹脂を使用した場合、
低発泡の成形品を得ることが困難であり、例え得られた
としてもビーズ間の融着に劣ったものとなり、押出品に
比較して、曲げ強度及び圧縮強度の小さいものしか得ら
れない欠点も有している。また射出成形法は、一段で発
泡成形品を得ることができるものの、通常この方法では
射出時に非常に高い圧力が必要であり、金型や押出機等
の設備を高い圧力に耐えられる構造にしなくてはなら
ず、そのため莫大な設備費が必要となる。この傾向は得
られる成形品を大型にしようとする程顕著に現われる。
また、発泡射出成形法では、機構上、発泡倍率でせいぜ
い2倍程度の成形品しか得ることができないという問題
があった。また、押出成形法では、型物を得ることがで
きないという欠点がある。Conventionally, the so-called bead molding method and foam injection molding method have been typical methods for producing a foamed thermoplastic resin molded product using a mold. However, since the bead molding method includes a two-stage foaming step in which beads obtained by pre-expanding the raw material resin particles are heated in the mold to be fused while being secondary-foamed and molded, the operation is complicated. Not only that, but also the shape of beads and traces of steam holes remain on the molded product,
It has the drawback of exhibiting poor appearance. Furthermore, in the bead molding method, especially when a polyolefin resin is used,
It is difficult to obtain a molded product with low foaming, and even if it is obtained, it will be inferior in fusion between beads, and compared to extruded products, only bending strength and compression strength can be obtained. I also have. In addition, although the injection molding method can obtain a foamed molded product in a single step, this method usually requires a very high pressure at the time of injection, and the equipment such as the mold and the extruder is not structured to withstand the high pressure. Must be avoided, and thus enormous equipment costs are required. This tendency becomes more remarkable as the obtained molded product is made larger.
Further, in the foam injection molding method, there is a problem that only a molded product having a foaming ratio of at most about 2 can be obtained due to the mechanism. Further, the extrusion molding method has a drawback that a molded product cannot be obtained.
そこで、本発明者らは、上記従来の樹脂型内発泡成形
法に見られるような欠点のない発泡成形法として、先
に、熱可塑性樹脂と発泡剤とを加圧下に溶融混練して発
泡性溶融物とした後、該溶融物をいったん発泡の生じな
い温度及び圧力条件に保持した後、間欠点に低圧域に押
出し、得られた押出溶融物を、該押出溶融物が未だ発泡
を完了しない間に、金型で成形すると共に、該金型内に
おいて発泡を完了させることを特徴とする発泡成形体の
製造方法を提案した(特願昭61−86730号)。Therefore, as a foam molding method which does not have the defects found in the conventional in-mold foam molding method, the present inventors first melt-knead a thermoplastic resin and a foaming agent under pressure to form a foam After being made into a melt, the melt was once held at a temperature and pressure conditions at which foaming did not occur, and then extruded into a low-pressure region due to an interim defect, and the obtained extruded melt did not yet complete foaming. In the meantime, a method for producing a foamed molded article has been proposed, which comprises molding with a mold and completing foaming in the mold (Japanese Patent Application No. 61-86730).
しかし、この方法においても、(1)成形に要する時
間が長い、(2)成形品コーナ部をシャープに出しにく
い、(3)成形品表面を平滑にしにくい等の問題を有
し、未だ改良の余地を残していた。However, even in this method, there are problems such as (1) it takes a long time for molding, (2) it is difficult to sharply form the corners of the molded product, and (3) it is difficult to smooth the surface of the molded product, and the improvement is still unsolved. There was room for it.
本発明は上記発泡成形法に見られるような問題のない
発泡成形法を提供することを目的とするものである。It is an object of the present invention to provide a foam molding method that does not have the problems found in the foam molding method.
本発明によれば、熱可塑性樹脂と発泡剤とを加圧下に
溶融混練して発泡性溶融物とした後、該溶融物をいった
ん発泡の生じない温度及び圧力条件に保持した後、低圧
域に押出し、得られた発泡過程にある押出溶融物に、該
押出溶融物が未だ発泡を完了しない間に衝撃を加え、型
内において発泡を完了させて成形することを特徴とする
発泡成形体の製造方法が提供される。According to the present invention, a thermoplastic resin and a foaming agent are melt-kneaded under pressure to form a foamable melt, and the melt is once held in a temperature and pressure condition where foaming does not occur, and then in a low pressure range. Production of a foamed molded article characterized by being extruded and impacted on the extruded melt obtained in the foaming process before the extruded melt has completed foaming to complete foaming in a mold. A method is provided.
本発明で原料として用いる熱可塑性樹脂としては、従
来公知のもの、例えば、各種ポリエチレン、ポリプロピ
レン、エチレンと他のモノオレフィン類(例えばプロピ
レン)との共重合体、エチレンとビニル単量体(例えば
酢酸ビニル)との共重合体等のポリオレフィン系樹脂及
びこれらのシラン変性物、ポリスチレン、ABS樹脂等の
スチレン系樹脂、その他ポリ塩化ビニル樹脂、各種ナイ
ロン樹脂、ポリカーボネート樹脂、ポリヒドロキシエー
テル樹脂等があり、これらは使用する用途において使い
分けられる。特に構造材料を得る場合には高密度ポリエ
チレンやポリプロピレンを使用することが好ましい。ま
た、上記樹脂を発泡させるための発泡剤は分解型発泡剤
あるいは溶剤型発泡剤のいずれでもよいが溶剤型のもの
が好ましく、特に好ましい具体例にはシクロブタン、シ
クロペンタン等の環式脂肪族炭化水素類、プロパン、ブ
タン、ペンタン、ヘキサン、ヘプタン等の脂肪族炭化水
素類、クロロジフロロメタン、トリクロロフルオロメタ
ン、ジクロロジフルオロメタン、ジクロロテトラフルオ
ロエタン、メチルクロライド、エチルクロライド、メチ
レンクロライド等のハロゲン化炭化水素類がある。なお
これらの発泡剤と共に、発泡助剤たとえば有機酸の金属
塩もしくは水素金属塩、炭酸の金属塩もしくは水素金属
塩、タルク等を併用してもよい。As the thermoplastic resin used as a raw material in the present invention, conventionally known resins, for example, various polyethylenes, polypropylenes, copolymers of ethylene and other monoolefins (for example, propylene), ethylene and vinyl monomers (for example, acetic acid). Vinyl) and other polyolefin resins such as copolymers, silane modified products thereof, polystyrene, styrene resins such as ABS resins, other polyvinyl chloride resins, various nylon resins, polycarbonate resins, polyhydroxy ether resins, etc., These are properly used depending on the intended use. In particular, when obtaining a structural material, it is preferable to use high-density polyethylene or polypropylene. The foaming agent for foaming the resin may be either a decomposing type foaming agent or a solvent type foaming agent, but a solvent type one is preferable, and a cycloaliphatic carbonization such as cyclobutane or cyclopentane is particularly preferable. Aliphatic hydrocarbons such as hydrogen, propane, butane, pentane, hexane, heptane, halogenation of chlorodifluoromethane, trichlorofluoromethane, dichlorodifluoromethane, dichlorotetrafluoroethane, methyl chloride, ethyl chloride, methylene chloride, etc. There are hydrocarbons. A foaming aid such as a metal salt or hydrogen metal salt of an organic acid, a metal salt or hydrogen metal salt of carbonic acid, or talc may be used together with these foaming agents.
次に、本発明の発泡成形品を得るための工程を図面を
参照しながら説明する。Next, steps for obtaining the foam-molded article of the present invention will be described with reference to the drawings.
図面において、Iは熱可塑性樹脂と発泡剤とを加圧下
で均一に溶融混練する工程を示すもので、通常の押出機
を用いて実施することができる。この場合、溶融混練温
度及び圧力は、熱可塑性樹脂の溶融混練に慣用されてい
る温度、圧力であり、樹脂の種類によって決まる。例え
ば、高密度ポリエチレンやポリプロピレンの場合、温度
120〜200℃、圧力30〜200kg/cm2Gの範囲の温度、圧力が
採用される。In the drawings, I indicates a step of uniformly melt-kneading a thermoplastic resin and a foaming agent under pressure, which can be carried out using an ordinary extruder. In this case, the melt-kneading temperature and pressure are the temperatures and pressures commonly used for melt-kneading thermoplastic resins, and are determined by the type of resin. For example, in the case of high density polyethylene or polypropylene, the temperature
Temperatures and pressures in the range of 120-200 ℃ and pressure of 30-200kg / cm 2 G are adopted.
前記溶融混練工程Iで得られた発泡性溶融物は、次
に、溶融物保持押出工程IIへ送られ、ここでいったんそ
の溶融物が発泡を生じない温度、圧力条件に保持される
と共に、ここから大気圧等の低圧帯域へ間欠的に押出さ
れ、溶融押出物Fとされる。発泡性溶融物を溶融混練工
程Iから溶融物保持押出工程IIへ送る場合、発泡性溶融
物は、通常、その温度を冷却により溶融温度より低く調
整して溶融物保持押出工程IIへ送るのが好ましい。例え
ば高密度ポリエチレンの場合には、上記温度を120〜170
℃とすることが好ましい。溶融物保持押出工程IIは、先
端にダイス4を有し、内部に往復運動する押出用ラム5
を備えた円筒状のアキュームレータ6を用いて実施する
ことができる。即ち、溶融混練工程からの溶融物がその
アキュームレータに設けられた連通孔よりアキュームレ
ーター内に圧入され、その際の圧力によりアラムはアキ
ュームレータ内を所定距離だけ後退し、アキュームレー
タ内には所定量の溶融物が充填される。この充填操作が
終了した後、ダイスを閉じていたゲートを開くと共に、
別に設けた液圧装置により、ラムとその液圧装置との間
に設けたピストンロッドを介して、ラムを押圧し、前進
させることによって、アキュームレータ内に保持された
溶融物をダイスを介して外部の低圧地帯へ押出する。こ
の押出し終了後、ゲートを閉じ、液圧装置の圧力を減
じ、ラムの押圧力を所定圧力にまで減少させることによ
り、再び前記のようにして溶融物がアキュームレータ内
に充填される。このようにしてアキュームレータから
は、溶融押出物Fが間欠的に押出される。アキュームレ
ータ内に溶融物を充填する際の圧力は、発泡を生じない
範囲の圧力であり、ラムに付加される押圧力により調節
される。The foamable melt obtained in the melt-kneading step I is then sent to a melt-holding extrusion step II, in which the melt is once held at a temperature and pressure conditions at which foaming does not occur, and Is intermittently extruded into a low pressure zone such as atmospheric pressure to obtain a melt extrudate F. When the foamable melt is sent from the melt-kneading step I to the melt-holding extrusion step II, the foamable melt is usually sent to the melt-holding extrusion step II with its temperature adjusted to be lower than the melting temperature by cooling. preferable. For example, in the case of high density polyethylene, the above temperature should be 120-170.
The temperature is preferably set to ° C. In the melt-holding extrusion step II, an extrusion ram 5 having a die 4 at its tip and reciprocating inside is formed.
It can be carried out by using a cylindrical accumulator 6 provided with. That is, the melt from the melt-kneading step is pressed into the accumulator through the communication hole provided in the accumulator, and the pressure at that time causes the alum to retreat within the accumulator by a predetermined distance and melts a predetermined amount in the accumulator. The thing is filled. After completing this filling operation, open the gate that closed the die,
A separately provided hydraulic device presses the ram through a piston rod provided between the ram and the hydraulic device, and advances the ram so that the melt held in the accumulator is externally passed through a die. Extrude into the low pressure zone. After this extrusion is completed, the gate is closed, the pressure of the hydraulic device is reduced, and the pressing force of the ram is reduced to a predetermined pressure, whereby the melt is charged into the accumulator again as described above. In this way, the melt extrudate F is intermittently extruded from the accumulator. The pressure at which the melt is filled in the accumulator is a pressure in the range where foaming does not occur, and is adjusted by the pressing force applied to the ram.
なお、前記溶融混練工程I及び溶融物保持押出工程II
を実施するための具体的装置については、特表昭57−50
1317号公報に詳記されている。The melt-kneading step I and the melt-holding extrusion step II
For specific equipment for carrying out
It is described in detail in Japanese Patent No. 1317.
前記のようにして、溶融物保持押出工程IIからは、間
欠的に溶融押出物Fが押出されるが、この溶融押出物F
は、必要により引取り装置によって順次引取られ、衝撃
工程IIIを経て成形工程IVへ送られ、ここで型にて所要
形状に成形される。As described above, the melt extrudate F is intermittently extruded from the melt-holding extrusion step II.
Are sequentially taken by a take-up device if necessary, and sent to a forming step IV through an impact step III, where they are formed into a desired shape by a mold.
衝撃工程IIIは、溶融押出物Fに物理的衝撃力を与え
得る方法であれば任意の方法で実施され、音波衝撃や圧
縮気体による衝撃、あるいは機械的打撃等を用いること
ができるが、特に機械的打撃を用いるのが好ましい。例
えば、第1図に示すように、溶融押出物Fを固定板8の
上に置き、打撃板7を下方に移動させて打撃することが
できる。この打撃操作は、溶融押出物Fの面積が著しく
拡大しないように、瞬時に行うのが好ましく、打撃後、
打撃板7を迅速に元の位置まで上昇させる。溶融押出物
Fに対する衝撃は、1回又は複数回にわたって行うこと
ができる。音波衝撃は、その音波による空気振動を溶融
押出物に与えることにより実施され、圧縮気体による衝
撃は圧縮気体を溶融押出物面に吹付けることにより実施
される。衝撃力の強さはできるだけ大きい方が好ましい
が、発泡過程にある溶融押出物F中の気泡を微細化し得
る程度の衝撃力であればよい。衝撃工程は、溶融押出物
Fの形成後、成形完了されるまでの任意の間で行うこと
ができる。例えば、第1図に示すように、溶融押出物F
を成形工程IVへ送る途中で行なったり、また、第2図に
示すように金型で締める時のプレス圧力により行なった
りすることができる。この衝撃処理により、発泡過程に
ある溶融押出物中には多数の細かい気泡が発生し、また
大きな気泡は微細な気泡に分割され、発泡力を増し、発
泡成形性にすぐれた溶融押出物とすることができる。The impact step III is carried out by any method as long as it is a method capable of giving a physical impact force to the melt extrudate F, and sonic impact, impact with a compressed gas, mechanical impact or the like can be used, but particularly mechanical It is preferable to use a physical impact. For example, as shown in FIG. 1, the molten extrudate F can be placed on the fixed plate 8 and the striking plate 7 can be moved downward to strike. This striking operation is preferably performed instantaneously so that the area of the melt extrudate F does not remarkably increase.
The striking plate 7 is quickly raised to its original position. The impact on the melt extrudate F can be performed once or multiple times. The sonic impact is performed by applying air vibrations due to the acoustic waves to the melt extrudate, and the impact by the compressed gas is performed by blowing the compressed gas onto the surface of the melt extrudate. It is preferable that the strength of the impact force is as large as possible, but the impact force may be such that bubbles in the melt extrudate F in the foaming process can be made fine. The impact step can be performed at any time after the formation of the melt extrudate F and before the completion of molding. For example, as shown in FIG.
Can be performed on the way to the molding step IV, or can be performed by pressing pressure when tightening with a mold as shown in FIG. Due to this impact treatment, a large number of fine bubbles are generated in the melt extrudate in the foaming process, and the large bubbles are divided into fine bubbles to increase the foaming power and form a melt extrudate having excellent foam moldability. be able to.
成形工程IVでは、衝撃を受けた溶融押出物Fが型内で
所要形状に成形されるが、この場合、使用される型とし
ては、成形性、離型性、生産性コスト等から、通常、金
型が用いられる。第2図に、溶融押出物Fを型内におい
て成形する場合の説明図を示す。第2図において、金型
12は、雄型9及び雌型10からなり、これらの型を合せた
時にできる空間が成形品の形状に対応する。まず雌型10
内に溶融押出物Fを入れる(第2図(a))。次に雌型
10を例えば1〜10kg/cm2(G)の圧力にて上昇させて、
押出溶融物を雄型9との間でプレスして空間部を埋める
(第2図(b))。この時プレス圧力を高く設定するこ
とにより、プレス時点より押出溶融物Fの発泡力を増大
させることができる。その後、押出溶融物Fの発泡膨張
によって徐々に雌型が押し広げられる(第2図
(c))。この押出溶融物の発泡膨張時には、その発泡
膨張の過程で雌型10に加えるプレス圧力をそのままの状
態あるいは低下させた状態で一定としたまま、発泡膨張
完了後低圧として冷却したり、あるいは発泡膨張力に応
じて徐々に雌型10のプレス圧力を低下させて、発泡膨張
完了後冷却したりする方法が採用される。この様な方法
では、押出溶融物Fの発泡膨張時における雌型10の設定
圧力を調整することにより、得られる成形品の発泡倍率
を容易にコントロールすることが可能となる。次に冷却
後、型開きを行って成形品を型内より取り出す(第2図
(d))。なお、第2図において、符号20は外部に通ず
る排気管及び符号21は連通孔を各示す。In the molding step IV, the impacted melt extrudate F is molded into a required shape in the mold. In this case, the mold used is usually moldability, mold release property, productivity cost, etc. A mold is used. FIG. 2 shows an explanatory diagram for forming the melt extrudate F in the mold. In Figure 2, the mold
12 is composed of a male mold 9 and a female mold 10, and the space formed when these molds are combined corresponds to the shape of the molded product. First female type 10
The melt extrudate F is put into the inside (FIG. 2 (a)). Then female
10 is raised at a pressure of, for example, 1 to 10 kg / cm 2 (G),
The extrusion melt is pressed with the male mold 9 to fill the space (FIG. 2 (b)). At this time, by setting the pressing pressure high, the foaming force of the extruded melt F can be increased from the time of pressing. After that, the female mold is gradually spread by the expansion and expansion of the extruded melt F (FIG. 2 (c)). At the time of foam expansion of this extruded melt, the press pressure applied to the female mold 10 in the process of foam expansion is maintained as it is or in a reduced state, and is cooled to a low pressure after completion of foam expansion, or foam expansion is performed. A method is employed in which the pressing pressure of the female mold 10 is gradually reduced according to the force to cool the female mold 10 after completion of foam expansion. In such a method, by adjusting the set pressure of the female mold 10 when the extruded melt F expands and expands, the expansion ratio of the obtained molded product can be easily controlled. Next, after cooling, the mold is opened to take out the molded product from the mold (Fig. 2 (d)). In FIG. 2, reference numeral 20 indicates an exhaust pipe communicating with the outside and reference numeral 21 indicates a communication hole.
本発明の方法を実施する場合、前記から明らかなよう
に、溶融押出物Fの発泡成形はその成形方式上型内にお
いて行われることから、型に装入した溶融押出物Fは、
未だ十分な発泡性を有するものでなければならない。従
って、溶融物保持押出工程IIから押出された発泡性溶融
押出物Fの発泡速度は遅い方が良く、且つ溶融押出物F
を迅速に衝撃工程IIIに送り、衝撃を加えて気泡を微細
にすることにより発泡力を高めた後、成形工程IVへ送
り、発泡と成形を完了させることが必要となる。溶融押
出物Fの気泡の大小及び発泡速度に影響を及ぼすその他
の因子としては、樹脂の種類及びメルトインデックス値
(MI値)、発泡剤の種類及び添加量等が挙げられるが、
特に発泡速度に関係するものは気泡調節剤の種類及び添
加量、ダイス吐出部断面の形状及び大きさであり、発泡
速度を遅くするには、ダイス吐出口断面を、溶融押出物
の押出直後のアキュームレーター内圧力と押出された雰
囲気下の圧力との差を小さくする形状及び大きさに選択
すること及び気泡調節剤の添加量を0または必要最小量
とすること等が挙げられる。例えば、樹脂としてMI値が
0.5〜20の高密度ポリエチレン(HDPE)を使用した場合
には、HDPE100重量部に対し、例えば、発泡剤としてト
リクロロトリフロロメタン又は/及びジクロロジフロロ
メタン等の発泡性発泡剤5〜20重量部、気泡調節剤とし
てタルク0〜0.05部添加し、押出機内において溶融混練
物とした後、該溶融混練物をアキュームレーター内に充
填し、押出すことにより好ましい発泡速度の溶融押出物
とすることができる。When carrying out the method of the present invention, as apparent from the above, since the foam molding of the melt extrudate F is performed in the mold due to its molding method, the melt extrudate F charged into the mold is
It must still have sufficient foamability. Therefore, the foaming speed of the foamable melt extrudate F extruded from the melt-holding extrusion step II should be low, and the melt extrudate F should be low.
Is rapidly sent to the impact step III to increase the foaming force by applying an impact to make the bubbles fine, and then sent to the molding step IV to complete the foaming and molding. Other factors that affect the size of the bubbles in the melt extrudate F and the foaming rate include the type of resin and the melt index value (MI value), the type of the foaming agent, and the amount added,
Particularly related to the foaming speed are the type and amount of the foam control agent, the shape and size of the cross section of the die discharge part, and in order to reduce the foaming speed, the cross section of the die discharge port should be prepared immediately after extrusion of the melt extrudate. Examples include selecting a shape and size that reduce the difference between the pressure in the accumulator and the pressure in the atmosphere under extrusion, and setting the amount of the cell regulator to be 0 or the necessary minimum amount. For example, the MI value of resin
When high density polyethylene (HDPE) of 0.5 to 20 is used, for example, 5 to 20 parts by weight of a foaming foaming agent such as trichlorotrifluoromethane or / and dichlorodifluoromethane as a foaming agent with respect to 100 parts by weight of HDPE. After adding 0 to 0.05 parts of talc as a foam control agent to obtain a melt-kneaded product in an extruder, the melt-kneaded product is filled in an accumulator and extruded to obtain a melt-extruded product having a preferable foaming rate. it can.
本発明の衝撃工程IIIにおいて、衝撃処理に付する溶
融押出物は、一般には、発泡率が80%以下、好ましくは
50%以下、特に好ましくは30%以下に保持するのがよ
い。なお、ここで言う発泡率とは、溶融押出物の押出直
後のアキュームレータ内圧力と押出された雰囲気圧との
差により、溶融押出物Fが発泡作用を起し、体積が膨張
し、その体積が最大となった場合を100とした相対体積
比を意味する。In the impact step III of the present invention, the melt extrudate subjected to impact treatment generally has a foaming rate of 80% or less, preferably
It is preferable to keep it at 50% or less, particularly preferably at 30% or less. Note that the foaming rate here means that the melt extrudate F causes a foaming action due to the difference between the internal pressure of the accumulator immediately after extrusion of the melt extrudate and the extruded atmosphere pressure, and the volume is expanded. It means the relative volume ratio when the maximum value is 100.
溶融物保持押出工程から得られる押出物の形状は特に
制限されず、必ずしも板状物である必要はなく、塊状物
又は棒状物であることもできる。このような塊状物は、
衝撃処理し、発泡を促進させ、整形することにより、型
の空間形状に応じた高品質の発泡成形品とすることがで
きる。The shape of the extrudate obtained from the melt-holding extrusion step is not particularly limited, and it does not necessarily have to be a plate-shaped product, and may be a lump-shaped product or a rod-shaped product. Such lumps are
By subjecting to impact treatment, promoting foaming, and shaping, it is possible to obtain a high-quality foam-molded article according to the space shape of the mold.
本発明によれば、パレット、床材、壁材、大型容器等
の強度の要求される大型の発泡構造材料を容易に製造す
ることができる。しかも、本発明の場合は、発泡性の溶
融物を型内で発泡成形することから、複雑な形状の発泡
成形品を容易に得ることができる。また、本発明によれ
ば、発泡射出成形法やビーズ成形法では得ることが困難
な発泡倍率が3〜10倍の成形品も含め、一般には、1.2
〜50倍という広範囲な発泡倍率を有する成形品も得るこ
とができる。また、発泡過程にある溶融押出物に衝撃処
理を行ったことから、発泡過程にある溶融押出物中には
多数の細かい気泡が発生し、また大きな気泡は微細な気
泡に分割され、発泡力を増し、発泡成形性にすぐれた溶
融押出物とすることができるので、得られた成形品は極
めて表面状態の優れたものとなる。According to the present invention, it is possible to easily manufacture a large-sized foam structural material such as a pallet, a flooring material, a wall material, and a large container, which requires strength. Moreover, in the case of the present invention, since the foamable melt is foam-molded in the mold, a foam-molded product having a complicated shape can be easily obtained. Further, according to the present invention, in general, a molded article having a foaming ratio of 3 to 10 times, which is difficult to obtain by the foaming injection molding method or the bead molding method, is 1.2.
Molded products having a wide expansion ratio of up to 50 times can also be obtained. Also, since the melt extrudate in the foaming process was subjected to impact treatment, many fine bubbles are generated in the melt extrudate in the foaming process, and the large bubbles are divided into fine bubbles to improve the foaming force. In addition, the melt-extruded product having excellent foam moldability can be obtained, and thus the obtained molded product has an extremely excellent surface condition.
また衝撃処理を受けた押出溶融物はその発泡速度をや
めることから、生産効率を向上させることができる。In addition, since the extruded melt that has been subjected to the impact treatment stops the foaming rate, the production efficiency can be improved.
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 described in more detail with reference to Examples.
実施例 密度0.96g/cm3、メルトインデックス(MI)5の高密
度ポリエチレン100重量部及びトリクロロトリフロロメ
タン4重量部を、吐出容量10kg/hrの押出機内で溶融混
練した後、140℃に樹脂温度を調整し、アキュームレー
タ内にいったん押出した。次にこのアキュームレータ内
に押出された発泡性溶融物を、300kg/hr(0.83kg/sec)
の吐出速度にて、そのアキュームレータに設けたダイス
(開口断面積15cm2)より大気圧下に板状に押出し、得
られた押出物380gを第2図に示す如くの上下動可能な雌
型(内底面積20cm×20cm)に入れた後、1.5kg/cm
2(G)の圧力で上昇させることにより、雄型と一致さ
せて押出物に衝撃を与え、その後徐々に雌型の圧力を低
下させて(低下に伴ない押出物はその発泡膨張力により
体積を増加する)、0.5kg/cm2(G)となった所で金型
を冷却し、成形品を取出した。得られた成形品は、密度
0.24g/cm3で体積1600ccのコーナ部がシャープに現われ
た直方体であった。また、このものは、良好な表面状態
を示し、表面部(スキン層)の気泡は微細かつ均一性の
良いものであった。Example 100 parts by weight of high density polyethylene having a density of 0.96 g / cm 3 and a melt index (MI) of 5 and 4 parts by weight of trichlorotrifluoromethane were melt-kneaded in an extruder having a discharge capacity of 10 kg / hr, and then the resin was heated to 140 ° C. The temperature was adjusted and once extruded into the accumulator. Next, the foamable melt extruded into this accumulator is 300kg / hr (0.83kg / sec)
At the discharge speed of, a die (opening cross-sectional area of 15 cm 2 ) provided in the accumulator was extruded into a plate shape under atmospheric pressure, and the extrudate 380 g obtained was vertically movable as shown in FIG. 1.5kg / cm after putting it in the inner bottom area 20cm × 20cm)
2 By increasing the pressure with (G), the extrudate is impacted in conformity with the male mold, and then the pressure of the female mold is gradually reduced (the extrudate is reduced in volume by its foaming expansive force as the pressure decreases). , And the mold was cooled at the place of 0.5 kg / cm 2 (G), and the molded product was taken out. The obtained molded product has a density
It was a rectangular parallelepiped with a sharp corner at 0.24 g / cm 3 and a volume of 1600 cc. Further, this product showed a good surface condition, and the bubbles in the surface portion (skin layer) were fine and had good uniformity.
また、比較のために、前記において打撃処理を行わな
い以外は同様にして実験を行ったところ、得られた成形
品は、コーナ部のシャープさに欠け、また成形品の表面
状態は本発明の成形品に比べて劣ったもので、表面部
(スキン層)の気泡は粗く、不均一のものであった。Further, for comparison, when an experiment was conducted in the same manner except that the hitting treatment was not performed in the above, the resulting molded product lacked the sharpness of the corner portion, and the surface condition of the molded product was the same as that of the present invention. It was inferior to the molded product, and the bubbles in the surface portion (skin layer) were coarse and non-uniform.
第1図は本発明を実施する場合の工程説明図である。第
2図は、溶融押出物の成形工程の説明図である。 I……溶融混練工程、II……溶融物保持押出工程、III
……衝撃工程、IV……成形工程、7……打撃板、12……
金型、F……溶融押出物。FIG. 1 is a process diagram for carrying out the present invention. FIG. 2 is an explanatory view of the forming process of the melt extrudate. I ... Melt-kneading process, II ... Melt-holding extrusion process, III
…… Impact process, IV …… Molding process, 7 …… Striking plate, 12 ……
Mold, F ... Melt extrudate.
Claims (5)
練して発泡性溶融物とした後、該溶融物をいったん発泡
の生じない温度及び圧力条件に保持した後、低圧域に押
出し、得られた発泡過程にある押出溶融物に、該押出溶
融物が未だ発泡を完了しない間に衝撃を加え、型内にお
いて発泡を完了させて成形することを特徴とする発泡成
形体の製造方法。1. A thermoplastic resin and a foaming agent are melt-kneaded under pressure to form a foamable melt, and the melt is once held at a temperature and pressure conditions where foaming does not occur, and then extruded into a low pressure region. A method for producing a foamed molded article, characterized in that the obtained extruded melt in the foaming process is subjected to impact while the extruded melt has not yet completed foaming to complete foaming in a mold. .
る特許請求の範囲第1項記載の製造方法。2. The production method according to claim 1, wherein the thermoplastic resin is a polyolefin resin.
特許請求の範囲第1項記載の製造方法。3. The manufacturing method according to claim 1, wherein the impact is applied by a striking plate or compression during mold clamping.
求の範囲第1項又は第2項記載の製造方法。4. The manufacturing method according to claim 1 or 2, wherein the impact is performed by a sound wave or a compressed gas.
用い、該高密度ポリエチレン100重量部に対し、揮発性
発泡剤5〜20重量部を用いる特許請求の範囲第1項〜第
4項記載のいずれかの方法。5. A high-density polyethylene is used as the thermoplastic resin, and 5 to 20 parts by weight of a volatile foaming agent is used with respect to 100 parts by weight of the high-density polyethylene, any of claims 1 to 4. That way.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62089940A JPH0813494B2 (en) | 1987-04-14 | 1987-04-14 | Method for producing foamed molded article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62089940A JPH0813494B2 (en) | 1987-04-14 | 1987-04-14 | Method for producing foamed molded article |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63256416A JPS63256416A (en) | 1988-10-24 |
JPH0813494B2 true JPH0813494B2 (en) | 1996-02-14 |
Family
ID=13984698
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62089940A Expired - Lifetime JPH0813494B2 (en) | 1987-04-14 | 1987-04-14 | Method for producing foamed molded article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0813494B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4242794A1 (en) * | 1991-12-18 | 1993-06-24 | Nitto Boseki Co Ltd | Quantitative automated determn. of 1,5-anhydro:glucitol - using pyranose oxidase from Basidiomycetes fungi no.52 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59232831A (en) * | 1983-06-16 | 1984-12-27 | Idemitsu Petrochem Co Ltd | Preparation of foaming thermoplastic resin |
-
1987
- 1987-04-14 JP JP62089940A patent/JPH0813494B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS63256416A (en) | 1988-10-24 |
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