JPH0717022B2 - Method for producing synthetic resin foam - Google Patents
Method for producing synthetic resin foamInfo
- Publication number
- JPH0717022B2 JPH0717022B2 JP1092291A JP9229189A JPH0717022B2 JP H0717022 B2 JPH0717022 B2 JP H0717022B2 JP 1092291 A JP1092291 A JP 1092291A JP 9229189 A JP9229189 A JP 9229189A JP H0717022 B2 JPH0717022 B2 JP H0717022B2
- Authority
- JP
- Japan
- Prior art keywords
- synthetic resin
- foam
- roll
- resin foam
- furnace
- 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 - Fee Related
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
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/3411—Relieving stresses
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は合成樹脂発泡体の製造方法に関するものであ
り、軽量かつ高断熱性能、高強度を有している板状の発
泡体を連続で押出し、一定の長さに切断し製品とする製
造方法に関する。TECHNICAL FIELD The present invention relates to a method for producing a synthetic resin foam, which is a plate-shaped foam that is lightweight and has high heat insulation performance and high strength and is continuously extruded. The present invention relates to a manufacturing method in which a product is cut into a certain length.
これらの合成樹脂発泡体は特性である軽量、高断熱性
能、高強度をいかし、主として建築用途の断熱材、床材
及び緩衝材の分野に効果的に使用できる。These synthetic resin foams can be effectively used mainly in the fields of heat insulating materials, flooring materials and cushioning materials mainly for construction purposes by taking advantage of their characteristics of light weight, high heat insulating performance and high strength.
従来の技術 従来、合成樹脂発泡体は押出機内で合成樹脂を発泡剤及
びその他の添加物と共に混合溶融、冷却した後、ダイ部
で高圧域から低圧域に圧力開放し成形装置により板状の
発泡体を成形していた。2. Description of the Related Art Conventionally, a synthetic resin foam is produced by mixing and melting a synthetic resin with a foaming agent and other additives in an extruder, cooling the mixture, and then releasing the pressure from a high pressure region to a low pressure region in a die part to form a plate-like foam by a molding device. I was shaping my body.
成形時においては発泡体をある一定の断面形状(例えば
厚み約20〜150mm×巾約1000mm)に成形しなくてはなら
ない。At the time of molding, the foam must be molded into a certain cross-sectional shape (for example, a thickness of about 20 to 150 mm x a width of about 1000 mm).
発明が解決しようとする問題点 しかしながら成形時において一定断面形状の発泡体を得
ようとするためには、例えば断面形状の大きな発泡体を
得ようとする場合には発泡体を成形金型内で滞流させ
る、すなわち押出方向であって向きが逆の力が加えら
れ、また断面形状の小さな発泡体を得ようとする場合に
は発泡体を引張りだす縦方向の力が加えられるため強度
がアンバランスな発泡体が得られていた。Problems to be Solved by the Invention However, in order to obtain a foam having a constant cross-sectional shape at the time of molding, for example, in the case of obtaining a foam having a large cross-sectional shape, the foam is placed in a molding die. The flow is stagnant, that is, the force is applied in the opposite direction but in the direction of extrusion, and in the case of obtaining a foam with a small cross-sectional shape, the longitudinal force pulling out the foam is applied, so the strength is A well-balanced foam was obtained.
ここで述べる強度とは圧縮強度をその評価項目とし、強
度バランスとは製品の厚み方向、巾方向、押出方向の3
方向のバランスとする。The strength described here is the compressive strength as its evaluation item, and the strength balance is 3 in the product thickness direction, width direction and extrusion direction.
Balance the direction.
この強度アンバランスは多々の不都合を生じる。例えば
巾、押出方向の強度が弱い場合、製品の寸法安定性、耐
熱性、また曲げ強度の低下となる。This imbalance in strength causes various inconveniences. For example, when the width and the strength in the extrusion direction are weak, the dimensional stability, heat resistance, and bending strength of the product decrease.
また厚み方向の強度が弱い場合、繰返し圧縮強度、局部
圧縮強度等の実用性能の低下となる。Further, when the strength in the thickness direction is weak, the practical performance such as repeated compression strength and local compression strength is deteriorated.
従来、この強度バランスはダイ直後の成形時でほぼ決定
されており、このバランスを調整するためにダイ形状、
温度、配合等を調整し成形してきたが効果的な調整方法
が得られなかった。Conventionally, this strength balance is almost determined at the time of molding immediately after the die, and in order to adjust this balance, the die shape,
Although the temperature and the composition were adjusted and molded, an effective adjusting method could not be obtained.
問題点を解決するための手段 本発明は従来技術の問題点を克服するうえで成形直後の
発泡体中には十分な発泡力が残存していることに注目
し、一旦発泡体を目的の形状に成形し、その後高温雰囲
気の炉を通過させ自由発泡を促進し、炉の出口に設置し
たロールで延伸成形することにより、ダイ直後の成形時
に加えられていた発泡体への歪を取除き、更には押出方
向への延伸を加えることで強度バランスが良好となる発
泡体を得ることを見出し本発明を完成した。MEANS FOR SOLVING PROBLEMS In the present invention, attention is paid to the fact that sufficient foaming power remains in a foam immediately after molding in order to overcome the problems of the prior art. To facilitate free foaming by passing through a furnace in a high temperature atmosphere, and by stretch molding with a roll installed at the exit of the furnace to remove the strain on the foam that was added during molding immediately after the die, Further, they have found that a foam having a good strength balance can be obtained by adding stretching in the extrusion direction, thus completing the present invention.
押出直後の発泡体を再加熱する方法は特公昭61−2497
6、特開昭63−37916及び特開昭63−159034に開示されて
いるが、これらはいずれも発泡体密度を低下せしめる方
法及び密度分布の均一化のための手段であって、押出直
後または表層部のみ冷却後発泡体を熱風、水蒸気、遠赤
外線の単独または併用により熱変形温度以上に再加熱
し、上記低密度化、密度分布均一化を達成しようとする
ものである。それに対し本発明は発泡体強度のアンバラ
ンスを支配するセル構造の異方性を変更させる手段とし
て、押出後の発泡体を再加熱しその後押出方向への延伸
成形を加えることで発泡体強度バランスを任意に調整し
ようとするものであり、前記先行技術とは異なるもので
ある。For the method of reheating the foam immediately after extrusion, see Japanese Examined Patent Publication No. 61-2497.
6, disclosed in JP-A-63-37916 and JP-A-63-159034, all of which are a method for reducing the foam density and a means for uniforming the density distribution, immediately after extrusion or After cooling only the surface layer part, the foam is reheated to a temperature not lower than the heat distortion temperature by using hot air, water vapor, or far infrared rays alone or in combination to achieve the above-mentioned low density and uniform density distribution. On the other hand, the present invention, as a means of changing the anisotropy of the cell structure that governs the imbalance of the foam strength, reheats the foam after extrusion and then stretch-molds in the extrusion direction to add the foam strength balance. Is intended to be adjusted arbitrarily, which is different from the prior art.
即ち、本発明は押出機内で合成樹脂を発泡剤及びその他
の添加物と共に混合溶融、冷却した後高圧域から低圧域
に圧力開放し合成樹脂発泡体を製造する方法において、
圧力開放直後に成形金型と第1ロールにより成形し、そ
の後内部が高温雰囲気に保たれた炉を通過させ、その出
口に設けた第2ロールにより再成形することを特徴とす
る合成樹脂発泡体の製造方法にある。That is, the present invention is a method for producing a synthetic resin foam by mixing and melting a synthetic resin with a foaming agent and other additives in an extruder, and then releasing the pressure from a high pressure region to a low pressure region after cooling.
Immediately after releasing the pressure, it is molded by a molding die and a first roll, then passed through a furnace whose inside is kept at a high temperature atmosphere, and remolded by a second roll provided at its outlet, which is characterized by being remolded. In the manufacturing method.
本発明による製造方法を図面を参照して説明する。A manufacturing method according to the present invention will be described with reference to the drawings.
ダイまでのプロセスは従来の慣用的な押出法である。ホ
ッパーより合成樹脂及び添加物を供給、途中発泡剤を混
入し高温、高圧下でスクリューにより混合溶融し押出機
内へ送る。その後発泡可能な樹脂粘度域まで冷却しダイ
へ送る。そのダイ(1)で高圧域から低圧域に圧力開放
し成形金型(2)と第1ロール(3)により所望の断面
形状を有する板状の発泡体を成形する。本発明によれ
ば、その後熱風発生装置(6)を備えた100〜160℃の範
囲で温度設定できる炉(5)の中を通過させ、第2ロー
ル(4)のスピードを調整し再加熱された発泡体に延伸
力を加え強度バランスをコントロールしながら発泡体を
得る。The process up to the die is conventional, conventional extrusion. Synthetic resin and additives are supplied from a hopper, and a foaming agent is mixed in the middle, mixed and melted by a screw under high temperature and high pressure, and sent into an extruder. After that, the resin is cooled to a foamable resin viscosity range and sent to a die. The die (1) is used to release the pressure from the high pressure region to the low pressure region, and a plate-shaped foam having a desired cross-sectional shape is molded by the molding die (2) and the first roll (3). According to the present invention, it is then reheated by passing through a furnace (5) equipped with a hot air generator (6) whose temperature can be set in the range of 100 to 160 ° C. and adjusting the speed of the second roll (4). Stretching force is applied to the foam to obtain a foam while controlling the strength balance.
炉内温度については発泡体の軟化点以上であり、かつ発
泡体表面がメルトしセルが破泡しない条件を満足する温
度範囲とし、好ましくは105〜160℃、更に好ましくは12
0〜140℃とする。The temperature in the furnace is equal to or higher than the softening point of the foam, and the temperature range satisfying the condition that the foam surface melts and the cell does not break, preferably 105 to 160 ° C, and more preferably 12
0 to 140 ℃.
炉の滞留時間については押出される発泡体の線速と炉の
長さによって決定され、目標とする強度調整範囲及び加
熱温度によってその必要滞留時間が決められるが少なく
とも30sec以上好ましくは45〜100secは必要である。The residence time of the furnace is determined by the linear velocity of the foam to be extruded and the length of the furnace, the required residence time is determined by the target strength adjustment range and heating temperature, but at least 30 seconds or more, preferably 45 to 100 seconds is is necessary.
第1,第2ロールのスピード比については得ようとする強
度バランス及び炉内温度条件により様々であるが、例え
ば第2ロールスピード/第1ロールスピードの比があま
りに大きければ炉内で発泡体が引きちぎれる等の問題点
が生じ、第2ロールスピード/第1ロールスピードの比
があまりに小さければ再加熱時の自由発泡により炉内で
発泡体が蛇行する等の問題点が生じる。The speed ratio of the first and second rolls varies depending on the strength balance to be obtained and the temperature conditions in the furnace. For example, if the ratio of the second roll speed / the first roll speed is too large, the foam in the furnace will be If the ratio of the second roll speed / the first roll speed is too small, the foam may meander in the furnace due to free foaming during reheating.
ゆえにロールスピード比の調整可能範囲として、好まし
くは第2ロールスピード/第1ロールスピード=1.1〜
1.6、更に好ましくは1.2〜1.4である。Therefore, the adjustable range of the roll speed ratio is preferably the second roll speed / the first roll speed = 1.1 to
1.6, and more preferably 1.2 to 1.4.
この発明方法において用いられるスチレン系樹脂はスチ
レン系単量体の単独重合体に限らず共重合体をも含んで
いる。The styrenic resin used in the method of the present invention includes not only a homopolymer of a styrenic monomer but also a copolymer.
スチレン系単量体にはスチレンのほかメチルスチレン、
エチルスチレン等も含まれる。また共重合体はスチレン
系単量体が50モル%以上含まれている共重合体を含んで
いる。共重合の相手方単量体としてはメタクリル酸メチ
ル等のメタクリル酸エステル、アクリル酸エステル、ア
クリル酸、メタアクリル酸、アクリロニトリル、無水マ
レイン酸等が挙げられる。これらの共重合体組成により
熱変形温度が変化する場合には炉内温度を調整し、目標
とする強度バランスを発現させることが可能である。Styrene monomers include styrene, methyl styrene,
Ethyl styrene and the like are also included. Further, the copolymer contains a copolymer containing 50 mol% or more of a styrene-based monomer. Examples of the partner monomer for copolymerization include methacrylic acid esters such as methyl methacrylate, acrylic acid esters, acrylic acid, methacrylic acid, acrylonitrile, and maleic anhydride. When the heat distortion temperature changes due to these copolymer compositions, it is possible to adjust the temperature in the furnace to develop a target strength balance.
この発明方法において用いられる発泡剤はスチレン系樹
脂の熱変形温度よりも低い沸点を持った脂肪族炭化水素
またはハロゲン化脂肪族炭化水素である。The blowing agent used in the method of the present invention is an aliphatic hydrocarbon or a halogenated aliphatic hydrocarbon having a boiling point lower than the heat distortion temperature of the styrene resin.
脂肪族炭化水素の例はプロパン、ブタン、ペンタン、ヘ
キサンのような飽和脂肪族炭化水素、およびプロピレ
ン、ブテン等の不飽和脂肪族炭化水素である。Examples of aliphatic hydrocarbons are saturated aliphatic hydrocarbons such as propane, butane, pentane, hexane, and unsaturated aliphatic hydrocarbons such as propylene, butene.
またハロゲン化脂肪族炭化水素の例はメチルクロライ
ド、メチレンクロライド、ジクロロジフルオロメタン、
テトラフルオロエタン、ジクロロテトラフルオロエタン
等である。Examples of halogenated aliphatic hydrocarbons are methyl chloride, methylene chloride, dichlorodifluoromethane,
Examples include tetrafluoroethane and dichlorotetrafluoroethane.
これらのものは単独でまたは2種以上のものを混合して
用いることができる。この発明方法においてセル径は押
出での造核剤量によって調整する。These may be used alone or in admixture of two or more. In the method of the present invention, the cell diameter is adjusted by the amount of nucleating agent in extrusion.
造核剤としては有機系(例えばステアリン酸バリウム、
ステアリン酸マグネシウム等)と無機系粉末(例えばタ
ルク)とを単独ないしはこれらの混合系で使用する。As a nucleating agent, organic type (for example, barium stearate,
Magnesium stearate or the like) and an inorganic powder (for example, talc) are used alone or in a mixed system thereof.
作 用 本発明の製造方法によれば用途ごとの要求性能に応じて
発泡体強度バランスをコントロールできるという柔軟な
生産ができ、また強度バランスを最適化することで性能
を維持しつつ軽量化がはかれコストダウンの効果があ
る。According to the production method of the present invention, it is possible to perform flexible production in which the foam strength balance can be controlled according to the required performance for each application, and by optimizing the strength balance, it is possible to reduce the weight while maintaining the performance. It has the effect of cost reduction.
次に本発明の合成樹脂発泡体の製造方法を実施例に基づ
いてさらに詳細に説明するが本発明はかかる実施例のみ
に限定されるものではない。Next, the method for producing the synthetic resin foam of the present invention will be described in more detail based on examples, but the present invention is not limited to these examples.
実施例1 樹脂としてポリスチレンを用いポリスチレン100部にタ
ルク1.0部を配合し押出機に供給した。発泡剤としてメ
チルクロライド6.0部とプロパン3.0部を押出機に圧入し
混合溶融した後、スリットダイより押出した。そして図
面に示す装置により炉内温度135℃、滞留時間52sec、第
1ロールと第2ロールの引取スピード比1.2の条件で厚
み110mm、巾1014mm、密度28kg/m3の発泡体を得た。Example 1 Using polystyrene as a resin, 100 parts of polystyrene and 1.0 part of talc were mixed and supplied to an extruder. As a foaming agent, 6.0 parts of methyl chloride and 3.0 parts of propane were pressed into an extruder, mixed and melted, and then extruded from a slit die. Using the apparatus shown in the drawing, a foam having a thickness of 110 mm, a width of 1014 mm and a density of 28 kg / m 3 was obtained under the conditions of a furnace temperature of 135 ° C., a residence time of 52 sec, and a take-up speed ratio of 1.2 between the first roll and the second roll.
この発泡体の諸物性を測定すると表1に示す物性値とな
り、比較例1にあげる値に比べてそのバランスが改善
し、曲げ強度、熱伝導率が向上していることがわかる。When the physical properties of this foam are measured, the physical properties shown in Table 1 are obtained, and it can be seen that the balance is improved and the bending strength and thermal conductivity are improved compared to the values given in Comparative Example 1.
比較例1 実施例1と同様にスリットダイより押出し、従来技術に
従って、炉および第2ロールを通過させることなく成形
し厚み120mm、巾1020mm、密度28kg/m3の発泡体を得た。Comparative Example 1 Extruded from a slit die in the same manner as in Example 1 and molded according to the conventional technique without passing through a furnace and a second roll to obtain a foam having a thickness of 120 mm, a width of 1020 mm and a density of 28 kg / m 3 .
実施例2 樹脂としてポリスチレンを用いポリスチレン100部にタ
ルク0.25部、ステアリン酸バリウム0.3部を配合し押出
機に供給した。発泡剤としてメチルクロライド5.5部と
プロパン2.0部を押出機に圧入し混合溶融した後、スリ
ットダイより押出した。そして図面に示す装置により炉
内温度130℃、滞留時間153sec、ロールスピード比1.00
〜1.16の条件で厚み約80mm、巾160mm、密度29〜30kg/m3
の発泡体を得た。Example 2 Using polystyrene as a resin, 0.25 parts of talc and 0.3 part of barium stearate were mixed with 100 parts of polystyrene and the mixture was supplied to an extruder. As a foaming agent, 5.5 parts of methyl chloride and 2.0 parts of propane were pressed into an extruder, mixed and melted, and then extruded from a slit die. Then, with the equipment shown in the drawing, the temperature inside the furnace was 130 ° C, the residence time was 153 seconds, and the roll speed ratio was 1.00.
~ 1.16 thickness about 80mm, width 160mm, density 29 ~ 30kg / m 3
A foam of
これらの発泡体の3方向に圧縮強度を測定すると表2に
示す物性値となり、第1ロールと第2ロールとのスピー
ド差で強度バランスがコントロールできる。When the compressive strengths of these foams are measured in three directions, the physical properties shown in Table 2 are obtained, and the strength balance can be controlled by the speed difference between the first roll and the second roll.
実施例3 樹脂としてポリスチレンを用いポリスチレン100部にタ
ルク1.0部を配合し押出機に供給した。発泡剤としてメ
チルクロライド6.0部とプロパン3.0部を押出機に圧入し
混合溶融した後、スリットダイより押出した。そして図
面に示す装置により炉内温度130℃、滞留時間55sec、ロ
ールスピード比1.2の条件で厚み約115mm、巾約1000mmの
発泡体を得た。Example 3 Using polystyrene as a resin, 100 parts of polystyrene and 1.0 part of talc were mixed and supplied to an extruder. As a foaming agent, 6.0 parts of methyl chloride and 3.0 parts of propane were pressed into an extruder, mixed and melted, and then extruded from a slit die. Then, using the apparatus shown in the drawing, a foam having a thickness of about 115 mm and a width of about 1000 mm was obtained under the conditions of a furnace temperature of 130 ° C., a residence time of 55 sec, and a roll speed ratio of 1.2.
この発泡体の諸物性を測定すると表3に示す物性値とな
り、2次発泡により軽量化されたにもかかわらず強度バ
ランスが改善し、曲げ強度、熱伝導率が向上しているこ
とがわかる。When the physical properties of this foam are measured, the physical properties shown in Table 3 are obtained, and it can be seen that the strength balance is improved and the bending strength and the thermal conductivity are improved despite the weight reduction due to the secondary foaming.
図面は本発明を実施するための装置の概略図である。 1はダイ、2は成形金型、3は第1ロール、4は第2ロ
ール、5は炉、6は熱風発生装置である。The drawing is a schematic representation of an apparatus for carrying out the invention. 1 is a die, 2 is a molding die, 3 is a first roll, 4 is a second roll, 5 is a furnace, and 6 is a hot air generator.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 B29L 7:00 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location B29L 7:00
Claims (5)
添加物と共に混合溶融、冷却した後高圧域から低圧域に
圧力開放し合成樹脂発泡体を製造する方法において、圧
力開放直後に成形金型と第1ロールにより成形し一旦表
層部を放冷した後、内部が高温雰囲気に保たれた炉を通
過させ、その出口に設けた第2ロールにより延伸成形す
ることを特徴とする合成樹脂発泡体の製造方法。1. A method for producing a synthetic resin foam by mixing and melting a synthetic resin together with a foaming agent and other additives in an extruder, cooling the mixture, and then releasing the pressure from a high pressure region to a low pressure region. Molded by a mold and a first roll, and once the surface layer is allowed to cool, it is passed through a furnace whose inside is kept in a high temperature atmosphere, and stretch-molded by a second roll provided at its outlet, which is a synthetic resin foaming. Body manufacturing method.
第2ロールの引取スピードを第2ロールが第1ロールの
1.1倍以上とし発泡体を押出方向に延伸させることを特
徴とする特許請求の範囲第1項記載の合成樹脂発泡体の
製造方法。2. The take-up speed of the first roll and the second roll installed across the heating furnace is controlled so that the second roll is the first roll.
The method for producing a synthetic resin foam according to claim 1, wherein the foam is stretched 1.1 times or more in the extrusion direction.
させることにより2次発泡させ、発泡体密度を低下せし
め、2次発泡により低下する強度物性を第2ロールでの
延伸成形で回復させることを特徴とする特許請求の範囲
第2項の合成樹脂発泡体の製造方法。3. The foam is subjected to secondary foaming by passing through a furnace kept in a high temperature atmosphere to reduce the foam density, and the strength properties which are degraded by the secondary foaming can be obtained by stretch molding with a second roll. The method for producing a synthetic resin foam according to claim 2, wherein the synthetic resin foam is recovered.
発泡体である特許請求の範囲第1〜3項のいずれかに記
載の合成樹脂発泡体の製造方法。4. The method for producing a synthetic resin foam according to any one of claims 1 to 3, wherein the synthetic resin foam is a polystyrene resin extruded foam.
ことを特徴とする特許請求の範囲第1〜4項のいずれか
に記載の合成樹脂発泡体の製造方法。5. The method for producing a synthetic resin foam according to any one of claims 1 to 4, wherein the inside of the furnace is kept in a high temperature atmosphere by heated air.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1092291A JPH0717022B2 (en) | 1989-04-11 | 1989-04-11 | Method for producing synthetic resin foam |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1092291A JPH0717022B2 (en) | 1989-04-11 | 1989-04-11 | Method for producing synthetic resin foam |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02270539A JPH02270539A (en) | 1990-11-05 |
| JPH0717022B2 true JPH0717022B2 (en) | 1995-03-01 |
Family
ID=14050312
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1092291A Expired - Fee Related JPH0717022B2 (en) | 1989-04-11 | 1989-04-11 | Method for producing synthetic resin foam |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0717022B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0767702B2 (en) * | 1992-10-16 | 1995-07-26 | バンドー化学株式会社 | Resin film heating device |
| CN105291411A (en) * | 2015-11-27 | 2016-02-03 | 厦门聚富塑胶制品有限公司 | Winding membrane stretching device |
| CN116175858B (en) * | 2023-03-03 | 2024-06-18 | 安徽乾泰新材料股份有限公司 | High-pressure foaming mixing device for expandable polystyrene filling resin |
-
1989
- 1989-04-11 JP JP1092291A patent/JPH0717022B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02270539A (en) | 1990-11-05 |
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