JPH06182891A - Manufacture of reclaimed foamed polystyrene series resin molded form - Google Patents

Manufacture of reclaimed foamed polystyrene series resin molded form

Info

Publication number
JPH06182891A
JPH06182891A JP4337554A JP33755492A JPH06182891A JP H06182891 A JPH06182891 A JP H06182891A JP 4337554 A JP4337554 A JP 4337554A JP 33755492 A JP33755492 A JP 33755492A JP H06182891 A JPH06182891 A JP H06182891A
Authority
JP
Japan
Prior art keywords
volume
foamed
resin particles
particles
expanded
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
JP4337554A
Other languages
Japanese (ja)
Other versions
JP2798572B2 (en
Inventor
Toshiki Ikeda
敏喜 池田
Shinpei Nakayama
新平 中山
Yasuhiro Ueda
靖博 上田
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.)
Sekisui Kasei Co Ltd
Original Assignee
Sekisui Plastics 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 Sekisui Plastics Co Ltd filed Critical Sekisui Plastics Co Ltd
Priority to JP4337554A priority Critical patent/JP2798572B2/en
Publication of JPH06182891A publication Critical patent/JPH06182891A/en
Application granted granted Critical
Publication of JP2798572B2 publication Critical patent/JP2798572B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

PURPOSE:To easily obtain a reclaimed foamed molded form of high quality with reduced consumption of heat energy without complicated step by pulverizing waste foamed polystyrene molded form, heat shrinking it to reduce in volume it, supplying it into a mold and introducing steam having a higher temperature than a softening point of a base material resin to heat it. CONSTITUTION:Waste foamed polystyrene series resin molded form is cleaned, and then pulverized to foamed resin particles of substantially spherical, stereoscopic state, etc., by a pulverizer, a cutter, etc. Its mean particle size is generally 5-50m and desirably about 10-30mm. Then, the particles are so heat shrinked to be reduced in volume in a range of 1-10min by using heated air as to become 75% or less of original bulky volume. The particles reduced in the volume are supplied into a mold, and steam of a temperature range higher by 10-40 deg.C than a Vicat softening temperature of the base material resin is introduced to heat it, thereby obtaining a foamed molded form.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は使用済の発泡ポリスチレ
ン系樹脂成形体、あるいは成形時に副生する不良品等の
廃発泡成形体を再生するための再生発泡ポリスチレン系
樹脂成形体の製造方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a regenerated expanded polystyrene resin molded product for recycling a used expanded polystyrene resin molded product or a waste expanded molded product such as a defective product produced as a by-product during molding. It is a thing.

【0002】[0002]

【従来の技術】発泡ポリスチレン系樹脂成形体は、家電
製品の緩衝包装材、あるいは魚介類や生鮮食品の運搬用
容器等として大量に使用されているが、その一方で、使
用済みの発泡成形体の廃棄処理対策が、社会的に大きな
問題となっている。そこで、近年では、使用済の発泡ポ
リスチレン系樹脂成形体を再生して、良好な発泡成形体
を製造することのできる発泡性ポリスチレン系の再生樹
脂粒子を得るために、種々の研究がなされている。
2. Description of the Related Art Expanded polystyrene resin moldings are used in large quantities as cushioning packaging materials for home electric appliances, containers for transporting seafood and fresh foods, and on the other hand, used foam moldings. Waste disposal measures have become a major social issue. Therefore, in recent years, various studies have been carried out in order to regenerate used expanded polystyrene resin molded articles to obtain expanded polystyrene regenerated resin particles capable of producing good expanded molded articles. .

【0003】従来の再生発泡性樹脂粒子を製造する方法
としては、使用済の発泡ポリスチレン系樹脂成形体を破
砕して、押出機により加熱溶融し、次いで、ダイスにて
押し出して冷却した後、切断してペレットを得、このペ
レットに水分散状態で、ブタン、ペンタン等の発泡剤を
含浸させて再生発泡性樹脂粒子を得る方法が知られてい
る。また、押出機内の溶融樹脂中に発泡剤を圧入して混
練し、ダイスにて押し出して冷却、切断することによ
り、再生発泡性樹脂粒子を製造する方法も公知である。
As a conventional method for producing regenerated expandable resin particles, a used expanded polystyrene resin molding is crushed, heated and melted by an extruder, then extruded with a die to be cooled, and then cut. There is known a method in which regenerated expandable resin particles are obtained by impregnating a pellet with a foaming agent such as butane or pentane in a water-dispersed state. Also known is a method of producing regenerated expandable resin particles by press-fitting a kneading agent into a molten resin in an extruder, kneading, extruding with a die, cooling and cutting.

【0004】[0004]

【発明が解決しようとする課題】ところが、上記の従来
の方法で製造された発泡性ポリスチレン系樹脂粒子を、
水蒸気により加熱発泡成形した再生発泡成形体では、気
泡が極端に細かくなり、耐熱性が低下するばかりでな
く、予備発泡粒子同士の密着性が悪いために、満足な成
形外観を有するものを得ることができない。また、この
発泡成形体は、機械的強度が低い等の欠点がある。
However, the expandable polystyrene resin particles produced by the above conventional method are
In a regenerated foamed molded product that is heat foamed with steam, not only the cells become extremely fine and the heat resistance deteriorates, but also the adhesion between the pre-foamed particles is poor, so that one having a satisfactory molded appearance is obtained. I can't. In addition, this foamed molded product has drawbacks such as low mechanical strength.

【0005】そこで特公昭58−24449号公報に
は、既に発泡したポリスチレン系樹脂粒子を原料とし
て、これに水分散状態で有機溶剤を加え、樹脂の軟化点
以上で攪拌した後、ブタン、ペンタン等の発泡剤を含浸
する方法が提案されている。また、特公昭58−244
50号公報には、同様の樹脂粒子を原料として、これに
水分散系でスチレン単量体を徐々に加えて発泡樹脂粒子
に吸収させ、加温して重合を行い、重合過程又は重合後
に、ブタン、ペンタン等の発泡剤を含浸する方法が提案
されている。しかし、これらの方法で得られた発泡性ポ
リスチレン樹脂粒子は、元の発泡成形体を構成する多数
の気泡が消失して、全く気泡のない樹脂粒子となってお
り、これを発泡成形して得られる発泡成形体の気泡状
態、機械的強度等は、ある程度改善されるものの、必ず
しも十分なものではない。しかも、これらの方法では、
発泡したポリスチレン系樹脂成形体を、一旦もとの非発
泡の樹脂粒子の状態に戻してから発泡性樹脂粒子として
再生するものであるため、工数がかかり、しかも多くの
熱エネルギーを必要とすることから、製造コスト的にも
不利である。
In Japanese Patent Publication No. 58-24449, therefore, polystyrene resin particles which have already been foamed are used as a raw material, an organic solvent is added thereto in a water-dispersed state, and the mixture is stirred above the softening point of the resin, butane, pentane, etc. The method of impregnating the foaming agent has been proposed. In addition, Japanese Examined Japanese Patent Sho 58-244
In JP-A-50, the same resin particles are used as a raw material, and a styrene monomer is gradually added to the resin particles in a water dispersion system so that the resin particles are absorbed and heated to carry out polymerization. A method of impregnating a foaming agent such as butane or pentane has been proposed. However, the expandable polystyrene resin particles obtained by these methods have a large number of bubbles constituting the original foam-molded body disappeared to become resin particles having no bubbles, which are obtained by foam-molding them. The foam state, mechanical strength, etc. of the foamed molded product obtained are improved to some extent, but are not always sufficient. And with these methods,
Since the expanded polystyrene resin molded product is restored to its original state of non-expanded resin particles and then regenerated as expandable resin particles, it takes man-hours and requires a lot of heat energy. Therefore, it is disadvantageous in terms of manufacturing cost.

【0006】このように従来の方法では、発泡成形体を
構成する気泡を一旦消失させて、気泡を含まない樹脂粒
子を製造するという行程を経るために、行程が複雑にな
るばかりでなく、加熱のために多くのエネルギーを消費
するとともに、加熱による樹脂の劣化によって、得られ
る再生発泡成形体の品質が低下するという問題点を有し
ている。
As described above, according to the conventional method, since the bubbles forming the foamed molded product are once eliminated to produce resin particles containing no bubbles, not only the process is complicated but also the heating is performed. Therefore, there is a problem that a lot of energy is consumed and the quality of the regenerated foamed molded product obtained is deteriorated due to deterioration of the resin due to heating.

【0007】本発明は、上記従来の問題点に鑑みなされ
たものであって、その目的は、使用済の発泡成形体を破
砕した発泡樹脂粒子を、従来の煩雑な工程を経ることな
しに、しかも多くの熱エネルギーを消費することなし
に、容易に高品質の再生発泡成形体を得る再生発泡ポリ
スチレン系樹脂成形体の製造方法を提供するものであ
る。
The present invention has been made in view of the above-mentioned conventional problems, and an object of the present invention is to provide a foamed resin particle obtained by crushing a used foamed molded product, without the conventional complicated steps. Moreover, the present invention provides a method for producing a regenerated expanded polystyrene resin molded product, which can easily obtain a high quality regenerated expanded molded product without consuming a large amount of heat energy.

【0008】[0008]

【課題を解決するための手段】本発明者等は、上記の課
題を解決するために、鋭意研究を重ねた結果、使用済の
発泡成形体を破砕した発泡樹脂粒子を、加熱空気で減容
化処理した後、成形型内に充填し、加熱成形することに
より、従来の煩雑な工程を経ることなしに、しかも多く
の熱エネルギーを消費することなしに、容易に高品質の
再生発泡成形体が得られることを見出し、本発明を完成
するに至ったものである。
Means for Solving the Problems The inventors of the present invention have conducted extensive studies in order to solve the above problems, and as a result, reduced the volume of foamed resin particles obtained by crushing a used foamed molded product with heated air. After the chemical treatment, it is filled in a molding die and heat-molded, so that a high-quality regenerated foamed molded product can be easily obtained without going through the conventional complicated process and consuming a large amount of heat energy. The present invention has been completed and the present invention has been completed.

【0009】すなわち、本発明の再生発泡ポリスチレン
系樹脂成形体の製造方法は、廃発泡ポリスチレン樹脂成
形体を破砕した発泡樹脂粒子を、元のカサ容積の75%
以下になるように加熱ガスを用いて熱収縮させて減容化
した後、減容化した樹脂粒子を成形型内に供給し、基材
樹脂のビカット軟化点よりも10〜40℃高い温度域の
水蒸気を導入して加熱することにより発泡成形体を得る
ことを特徴としている。
That is, according to the method for producing a recycled expanded polystyrene resin molded product of the present invention, the expanded resin particles obtained by crushing the waste expanded polystyrene resin molded product are 75% of the original bulk volume.
After the volume is reduced by heat-shrinking using a heating gas as shown below, the volume-reduced resin particles are supplied into the molding die, and the temperature range is 10 to 40 ° C. higher than the Vicat softening point of the base resin. It is characterized in that a foamed molded article is obtained by introducing and heating the above steam.

【0010】また、本発明は、廃発泡ポリスチレン系樹
脂成形体を破砕し減容化した発泡樹脂粒子に、その粒子
が合着しない緩和な温度下で、かつ加圧下において発泡
樹脂粒子を、成形型内充填後の発泡樹脂粒子のカサ容積
が元のカサ容積の80%以下になるように加圧ガスを用
いて圧縮しながら成形型内に供給し、基材樹脂のビカッ
ト軟化点よりも10〜40℃高い温度域の水蒸気を導入
して加熱融着させて発泡成形体を得ることを特徴として
いる。
Further, according to the present invention, the foamed resin particles obtained by crushing and reducing the volume of the waste expanded polystyrene resin molded article are molded into foamed resin particles under a moderate temperature at which the particles do not coalesce and under pressure. The foamed resin particles after being filled in the mold were supplied into the molding mold while being compressed using a pressurized gas so that the bulk volume of the foamed resin particles was 80% or less of the original bulk volume, and the pressure was 10 higher than the Vicat softening point of the base resin. It is characterized in that a foamed molded product is obtained by introducing steam in a temperature range higher by -40 ° C and heating and fusing.

【0011】本発明において、その出発原料として用い
られる廃発泡ポリスチレン系樹脂成形体を構成する樹脂
としては、スチレン重合体、少なくとも50重量%以上
のスチレン成分と他の重合可能な不飽和化合物との共重
合体、これらの混合樹脂、スチレンとポリエチレンある
いはポリプロピレンとの架橋重合体、並びにこれらの樹
脂に適量のゴム状物質を添加した強化樹脂等が挙げられ
る。上記の共重合可能な不飽和化合物としては、α−メ
チルスチレン、アクリロニトリル、アクリル酸もしくは
メタクリル酸と1〜8個の炭素原子を有するアルコール
とのエステル、マレイン酸、フマル酸と1〜8個の炭素
原子を有するアルコールとのエステル、無水マレイン酸
等や、さらに少量の架橋剤として、ジビニルベンゼン、
ブタジエン、ポリエチレングリコ−ルジメタクリレート
等も挙げることができる。
In the present invention, the resin constituting the waste expanded polystyrene resin molding used as the starting material is a styrene polymer, at least 50% by weight or more of a styrene component and another polymerizable unsaturated compound. Examples thereof include copolymers, mixed resins thereof, cross-linked polymers of styrene and polyethylene or polypropylene, and reinforced resins obtained by adding an appropriate amount of a rubber-like substance to these resins. Examples of the above-mentioned copolymerizable unsaturated compound include α-methylstyrene, acrylonitrile, an ester of acrylic acid or methacrylic acid and an alcohol having 1 to 8 carbon atoms, maleic acid, fumaric acid and 1 to 8 Esters with alcohols having carbon atoms, maleic anhydride, etc., and as a small amount of a crosslinking agent, divinylbenzene,
Butadiene, polyethylene glycol dimethacrylate, etc. may also be mentioned.

【0012】上記の廃発泡ポリスチレン系樹脂成形体に
は、上記のポリスチレン系樹脂の粒子に発泡剤を含浸さ
せた発泡性樹脂粒子を、予備発泡した後、所定の成形型
内で発泡成形して得られた発泡成形体であって、各種容
器、緩衝包装材、その他一定の用途に供された後の、使
用済みの廃棄されるべき発泡成形体、及びこれらの成形
体を製造するときに副生する成形不良品等が含まれる。
なお、廃発泡ポリスチレン系樹脂成形体としては、必ず
しも所定の成形型内で発泡成形して得られた発泡成形体
に限らず、上記の樹脂を押出発泡して得られた発泡成形
体の使用済み成形体、成形不良品、トリミング時の裁断
屑等を原料とすることも可能である。また、発泡成形体
を構成する樹脂中には、充填剤、可塑剤、難燃剤、滑
剤、着色剤、紫外線吸収剤、酸化防止剤等、種々の添加
剤が含有されていてもよい。
The above-mentioned waste expanded polystyrene resin molded article is pre-expanded with expandable resin particles obtained by impregnating the above polystyrene resin particles with a foaming agent, and then foam-molded in a predetermined molding die. The obtained foamed molded article, which has been used for various containers, cushioning packaging materials, and certain other purposes, and has been used for disposal, and a secondary molded article when these molded articles are manufactured. Includes raw defective products.
The waste expanded polystyrene resin molded product is not limited to the foamed molded product obtained by foaming and molding in a predetermined molding die, but the foamed molded product obtained by extruding and foaming the above resin has been used. It is also possible to use a molded product, a defective molded product, a cutting waste during trimming, or the like as a raw material. In addition, various additives such as a filler, a plasticizer, a flame retardant, a lubricant, a colorant, an ultraviolet absorber and an antioxidant may be contained in the resin forming the foamed molded article.

【0013】さらに、本発明において、出発原料として
用いる廃発泡ポリスチレン系樹脂成形体の基材樹脂は、
単一の樹脂種を使用することが望ましいが、発泡成形体
の熱的性質(発泡成形性)、気泡サイズ(成形品外観)
がほぼ同等であれば、2種以上の基材樹脂を混合して使
用することもできる。
Further, in the present invention, the base resin of the waste expanded polystyrene resin molding used as a starting material is
It is desirable to use a single resin type, but the thermal properties of the foam molded product (foam moldability), cell size (molded product appearance)
Can be used by mixing two or more kinds of base resins.

【0014】また、廃発泡ポリスチレン系樹脂成形体
は、その用途に応じて発泡倍数が異なるが、本発明方法
によって均質な再生発泡成形体を得るためには、ほぼ同
じ発泡倍数の成形体を分別して原料として使用すること
が望ましい。廃発泡成形体の大半を占める家電製品の緩
衝包装材、魚介類用容器、リンゴ箱等は、およそ発泡倍
数50〜60倍の発泡成形体である。しかし、この程度
のばらつき範囲内であれば、本願の原料として特に支障
なく使用することができる。
Further, the waste expanded polystyrene resin molded product has a different foaming multiple depending on its use, but in order to obtain a homogeneous regenerated foamed molded product by the method of the present invention, moldings having substantially the same foaming multiple are separated. It is desirable to use it separately as a raw material. The cushioning packaging material for home electric appliances, the container for seafood, the apple box, etc., which occupy most of the waste foamed molded product, is a foamed molded product having a foaming multiple of 50 to 60 times. However, if it is within such a variation range, it can be used as the raw material of the present application without any trouble.

【0015】次に、再生発泡ポリスチレン系樹脂成形体
の製造方法について以下に述べる。
Next, a method for producing a regenerated expanded polystyrene resin molding will be described below.

【0016】まず、上記の廃発泡ポリスチレン系樹脂成
形体は、洗浄等された後、破砕機あるいは裁断機、その
他任意の方法により、ほぼ球状、あるいは立方体状等の
形状を有する発泡樹脂粒子に破砕される。発泡樹脂粒子
の平均粒子径は、再生発泡成形する成形体の大きさによ
り適宜決められるが、一般的には、5〜50mmであ
り、好ましくは10〜30mm程度である。平均粒子径
が50mmよりも大きい場合には、空気輸送時に配管が
詰まったり、成形型への充填性が悪くなる。一方、平均
粒子径が5mmよりも小さい場合には、発泡成形体の破
砕時に発泡成形体の内部の気泡が破壊されて、独立気泡
率が低下し、発泡成形時に十分な発泡性が得られず正常
な発泡成形体が得られない。
First, the waste expanded polystyrene resin molded product is washed and the like, and then crushed by a crushing machine or a cutting machine or any other method into foamed resin particles having a substantially spherical shape or a cubic shape. To be done. The average particle diameter of the foamed resin particles is appropriately determined according to the size of the molded body to be refoamed and molded, but is generally 5 to 50 mm, preferably about 10 to 30 mm. If the average particle size is larger than 50 mm, the pipes may be clogged during pneumatic transportation and the moldability may be poor. On the other hand, when the average particle size is smaller than 5 mm, the bubbles inside the foamed molded product are destroyed when the foamed molded product is crushed, the closed cell ratio is lowered, and sufficient foamability cannot be obtained during foamed molding. A normal foam molding cannot be obtained.

【0017】本発明で使用する発泡樹脂粒子の独立気泡
率は、65%以上、好ましくは80%以上であることが
必要である。発泡成形体を破砕するときに発生する不適
当な微粒子が多量に含まれる場合は、ふるい分けして微
粒子を除去することが望ましい。また破砕機あるいは裁
断機としては、発泡成形体の気泡をできるだけ破壊しな
いで、しかも微細粒子の発生を抑え、粒子径が揃い、球
状あるいは立方体に近い形状の所望の発泡粒子が得られ
るものが好適に使用される。
The closed cell ratio of the expanded resin particles used in the present invention must be 65% or more, preferably 80% or more. When a large amount of inappropriate fine particles generated when the foamed molded product is crushed, it is desirable to remove the fine particles by sieving. Further, as a crusher or a cutter, a crusher or a crusher which does not break the bubbles of the foamed molded article as much as possible, suppresses the generation of fine particles, has a uniform particle size, and can obtain desired foamed particles having a spherical shape or a shape close to a cube is preferable. Used for.

【0018】次いで、上記発泡樹脂粒子を、加熱空気を
用いて減容化する。発泡粒子の減容化処理は、基材樹脂
のビカット軟化点(TS )よりも10℃〜60℃高い温
度、好ましくは25℃〜50℃高い温度範囲で行われ
る。好ましい温度域は、使用する発泡樹脂粒子の基材樹
脂によって変化するが、ビカット軟化点+10℃よりも
温度が低いと、減容化に長時間を要し実用化が難しい。
一方、ビカット軟化点+60℃よりも高い温度では、発
泡粒子同士が合着し、また減容が急激に過ぎて量産的に
正常な均一な減容化が行い難い。
Next, the expanded resin particles are reduced in volume by using heated air. The volume reduction treatment of the expanded beads is performed at a temperature higher by 10 ° C. to 60 ° C., preferably 25 ° C. to 50 ° C. higher than the Vicat softening point (T S ) of the base resin. The preferred temperature range varies depending on the base resin of the expanded resin particles to be used, but if the temperature is lower than the Vicat softening point + 10 ° C, it takes a long time to reduce the volume and it is difficult to put it into practical use.
On the other hand, at a temperature higher than the Vicat softening point + 60 ° C., the expanded particles are coalesced with each other, and the volume reduction is so rapid that it is difficult to achieve a uniform volume reduction that is normal for mass production.

【0019】上記の温度条件下においては、発泡樹脂粒
子同士が合着する恐れはないことから、発泡粒子を容器
内に静置した状態で加熱空気を導入するか、あるいは、
加熱空気槽内に発泡粒子を導入することにより減容化処
理を行うことができる。また発泡粒子を容器内に入れ、
容器を回転させるか、もしくは容器内に設置された攪拌
手段にて攪拌しながら加熱空気を導入して減容化処理を
実施してもよい。
Under the above temperature conditions, there is no risk of the expanded resin particles sticking to each other. Therefore, the heated air is introduced while the expanded particles are left in the container, or
The volume reduction treatment can be performed by introducing the expanded particles into the heated air tank. Also put the foamed particles in the container,
The volume reduction treatment may be performed by rotating the container or introducing heated air while stirring with a stirring means installed in the container.

【0020】減容化処理に要する時間は、基材樹脂の種
類、加熱空気の温度、及び加熱空気の供給量などにより
適宜変更して実施されるが、一般的に1〜10分程度の
範囲であり、より好ましくは2〜5分である。処理時間
が1分よりも少ないと減容が急激に行われ量産的に均一
性が得難くなり、逆に10分を越えると生産性の低下を
来たし好ましくない。
The time required for the volume reduction treatment is appropriately changed depending on the type of the base resin, the temperature of the heated air, the supply amount of the heated air, etc., but it is generally in the range of about 1 to 10 minutes. And more preferably 2 to 5 minutes. When the treatment time is less than 1 minute, the volume is rapidly reduced and it becomes difficult to obtain uniformity in mass production. On the contrary, when it exceeds 10 minutes, the productivity is deteriorated, which is not preferable.

【0021】ここで、通常の予備発泡粒子の空間率は、
約35〜40%である。これに対して、本発明で使用さ
れる廃発泡ポリスチレン系樹脂粒子体を破砕した発泡樹
脂粒子は、カサ容積が大きく、空間率は約50〜60%
となる。
Here, the porosity of ordinary pre-expanded particles is
It is about 35-40%. On the other hand, the expanded resin particles obtained by crushing the waste expanded polystyrene resin particles used in the present invention have a large bulk volume and a porosity of about 50 to 60%.
Becomes

【0022】したがって、比較的低い発泡倍数(およそ
40倍以下)の成型品を再生製造する場合、破砕発泡性
樹脂粒子の加熱空気による減容を減容比50%以下、3
0%以上の範囲で大きくして、そのまま成形型に通常の
方法で充填を行い、成型することができる。
Therefore, when a molded product having a relatively low expansion ratio (about 40 times or less) is remanufactured, the volume reduction of the crushed expandable resin particles by the heated air is reduced by 50% or less, 3 or less.
It can be molded by increasing the content in the range of 0% or more and filling the mold as it is with a usual method.

【0023】一方、比較的高い発泡倍数(およそ50倍
以上)の成型品を再生製造する場合、破砕発泡性樹脂粒
子の加熱空気による減容を減容比60%以上、75%以
下に小さくして、加熱空気で減容破砕発泡性樹脂粒子を
80%以下、60%以上のカサ容量に圧縮して成形型に
充填した後、成形型内の加熱空気を除圧し、成形型内に
圧縮充填された発泡粒子容量を回復させて粒子間の空隙
率を40%以下にして、水蒸気にて加熱成形することに
より相互に融着させ、成形型通りの成形体を得ることが
できる。
On the other hand, when a molded product having a relatively high expansion ratio (about 50 times or more) is remanufactured, the volume reduction of the crushed expandable resin particles by the heated air is reduced to a volume reduction ratio of 60% or more and 75% or less. Then, the volume-reduced crushable expandable resin particles are compressed to 80% or less and 60% or more of the bulk capacity with heated air and filled in the mold, then the heated air in the mold is depressurized and compressed into the mold. It is possible to recover the volume of the foamed particles so that the porosity between the particles is 40% or less, and heat-mold with steam to fuse them to each other to obtain a molded product as a molding die.

【0024】そして、本発明において、比較的高い発泡
倍数の成形品を再生するときは、圧縮の程度は、減容後
のカサ容積の80%以下、好ましくは70%以下、60
%以上である。圧縮がカサ容積の80%に満たないとき
は、加熱成形時に発泡力が得られず、正常な成形体が得
難い。
In the present invention, when a molded product having a relatively high expansion ratio is regenerated, the degree of compression is 80% or less, preferably 70% or less, 60% of the volume of the bulk after volume reduction.
% Or more. If the compression is less than 80% of the bulk volume, the foaming force cannot be obtained during heat molding, and it is difficult to obtain a normal molded product.

【0025】次いで、加熱成形は、成形型に加圧水蒸気
を導入することにより行われる。すなわち、上記の減容
発泡樹脂粒子中の空気と加熱水蒸気との分圧によって、
減容発泡樹脂粒子が所定の発泡倍数に発泡する。
Next, heat molding is carried out by introducing pressurized steam into the mold. That is, by the partial pressure between the air and the heated steam in the volume-reduced expanded resin particles,
The reduced-volume expanded resin particles expand to a predetermined expansion ratio.

【0026】上記の水蒸気は基材樹脂のビカット軟化点
よりも10〜40℃高い温度域になるように制御され、
より好ましくはビカット軟化点よりも15〜30℃高い
温度範囲に調整される。加熱成形時の水蒸気温度がビカ
ット軟化点+10℃よりも低い温度域では、発泡速度が
遅くなり発泡粒子内の空気の外部への逸散が優位となっ
て充分な発泡効果が得られず、その結果、高品質の発泡
成形体が得られない。
The above-mentioned water vapor is controlled so as to be in a temperature range 10 to 40 ° C. higher than the Vicat softening point of the base resin,
More preferably, the temperature is adjusted to a temperature range 15 to 30 ° C. higher than the Vicat softening point. In the temperature range where the water vapor temperature at the time of heat molding is lower than the Vicat softening point + 10 ° C., the foaming speed becomes slow and the air inside the foamed particles escapes to the outside so that a sufficient foaming effect cannot be obtained. As a result, a high quality foamed molded product cannot be obtained.

【0027】また、ビカット軟化点+40℃を越える温
度域では、発泡適性幅が極めて狭くなり、工業的に正常
な発泡成形体を得ることが極めて困難である。なお、加
熱成形に要する時間は、得ようとする発泡成形体の大き
さや発泡倍数等によって変化するが、一般的に10〜1
80秒であり、好ましくは約15〜90秒程度である。
また、水蒸気としては、水蒸気−空気混合媒体を用いる
ことも可能である。
Further, in the temperature range exceeding the Vicat softening point + 40 ° C., the foaming suitability range becomes extremely narrow, and it is extremely difficult to obtain an industrially normal foamed molded product. The time required for heat-molding varies depending on the size of the foam-molded product to be obtained, the expansion ratio, etc., but is generally 10 to 1
It is 80 seconds, preferably about 15 to 90 seconds.
Further, as the water vapor, it is also possible to use a water vapor-air mixed medium.

【0028】なお、本発明においては、発泡樹脂粒子の
圧縮状態を維持するために、発泡樹脂粒子の充填前、及
び充填中の成形型内を、加圧状態に維持しておくことが
望ましい。発泡樹脂粒子を加熱成形して得られる再生発
泡成形体の発泡倍数は、元の廃発泡樹脂成形体の発泡倍
数と、加圧下の発泡樹脂粒子の圧縮率で決まり、成形型
内での発泡粒子のカサ倍数が、再生発泡成形体の発泡倍
数となる。したがって、成形型内の内圧を、予め所定の
加圧状態に設定しておいて、発泡樹脂粒子を加圧充填す
る必要がある。上記の発泡樹脂粒子の加圧充填、及び成
形型内の加圧に用いるガスとしては、気相含浸時に用い
る無機ガスを使用できるが、通常は圧縮空気が好適に使
用される。
In the present invention, in order to maintain the compressed state of the expanded resin particles, it is desirable to maintain the pressure inside the mold before and during the filling of the expanded resin particles. The expansion ratio of the recycled foamed molded product obtained by heat-molding the expanded resin particles is determined by the expansion ratio of the original waste expanded resin molded product and the compression ratio of the expanded resin particles under pressure, and the expanded particles in the molding die The multiplication factor of is the foaming factor of the recycled foam molded article. Therefore, it is necessary to set the internal pressure in the molding die to a predetermined pressurization state in advance and press-fill the expanded resin particles. As the gas used for the pressure filling of the foamed resin particles and the pressurization in the molding die, an inorganic gas used at the time of vapor phase impregnation can be used, but normally compressed air is preferably used.

【0029】その後、成形型の加圧状態を解放して圧抜
きをすることによって成形型の内圧を大気圧に戻し、発
泡粒子間のガスを排出すると共に、圧縮された発泡粒子
を膨張復元した後、成形型に水蒸気を導入して発泡粒子
を加熱融着させて、発泡成形体を成形する。加熱成形し
て得られた発泡成形体は、冷却水により冷却した後、成
形型から取り出せる。
After that, the pressure inside the mold is released and the pressure is released to return the internal pressure of the mold to the atmospheric pressure, the gas between the expanded particles is discharged, and the compressed expanded particles are expanded and restored. Then, steam is introduced into the mold to heat and fuse the expanded particles to form an expanded molded body. The foamed molded product obtained by heat molding can be taken out from the mold after being cooled with cooling water.

【0030】以上のようにして得られた再生発泡成形体
は、建築用途の断熱壁材や軽量材や床下地材、又は土木
用途の軟弱地盤改良用ESPや土木工法の埋設材等とし
て好適に使用される。これらの用途においては、再生発
泡成形体は比較的肉厚なブロック形状、あるいは板状の
形状とされ、特に複雑な形状に成形する必要のないこと
から、何等支障なく使用することができる。また、これ
らの用途において望まれる発泡成形体の発泡倍数は、4
0〜50倍程度であって、使用済の家電製品の緩衝包装
材、あるいは魚介類や生鮮食品の運搬容器等を、本発明
の原料として好適に使用することができる。
The regenerated foamed molded product obtained as described above is suitable as a heat insulating wall material for construction purposes, a lightweight material, a floor base material, an ESP for improving soft ground for civil engineering applications, an embedding material for civil engineering methods, etc. used. In these applications, the regenerated foamed molded product has a relatively thick block shape or plate shape, and since it does not need to be molded into a particularly complicated shape, it can be used without any trouble. In addition, the foaming multiple of the foamed molded product desired in these applications is 4
It is about 0 to 50 times, and a buffer packaging material for used home electric appliances, a transportation container for seafood or fresh food, and the like can be preferably used as the raw material of the present invention.

【0031】なお、本発明により得られた再生発泡成形
体を、上記の建築用途あるいは土木用途に使用する場合
には、発泡成形体に自消性、難燃性を付与することが必
要となる。再生発泡成形体に自消性、難燃性を付与する
には、発泡樹脂粒子の表面に、難燃剤あるいは必要に応
じて難燃助剤を加えて被覆処理したものを、発泡成形す
ればよい。難燃剤としては、臭素化脂環族化合物、臭素
化芳香化合物、臭素化芳香族ポリマー、臭素化フェニル
(メタ)アクリル酸エステル等が好適に使用される。上
記の難燃剤が粉末状の場合、JIS標準ふるい149μ
m通過の微粉末を使用することが、粒子表面への付着性
の面から望ましい。また、粒子に対する付着を確実にす
るために、適度な粘性を有する液状難燃剤を一部被覆し
た後に、粉末状難燃剤を被覆展着処理してもよい。さら
に比較的低融点を有する粉末状難燃剤を、加温して溶解
させて被覆処理してもよい。このような難燃剤の具体例
としては、比較的少量の使用で自消性をもたらし、発泡
樹脂粒子表面への付着性がよく、成形時に発泡粒子間の
融着を阻害せず、耐候性がよく、しかも樹脂基材を劣化
させないものとして、ヘキサブロモシクロドデカン、テ
トラブロモシクロオクタン、トリブロモフェニルアリル
エーテル、ペンタブロモフェニルアリルエーアル、テト
ラブロモビスフェノールのビスアリルエーテル、テトラ
ブロモビスフェノールのビスジブロモプロピルエーテル
等が、特に好適に使用される。これらの難燃剤は、発泡
樹脂粒子に対して0.5〜2.0重量%、より好ましく
は0.8〜1.5重量%の範囲で使用される。また、有
機過酸化物等の、例えばO−O、C−C、N=N結合を
有する化合物を難燃助剤として、0.1〜0.5重量%
の難燃剤と併用して使用してもよい。好ましい難燃助剤
の例としては、ジクミルパーオキサイド、1,1−ジフ
ェニルビシクロヘキシル、アゾジイソブチロニトリル等
が挙げられる。
When the recycled foamed molded product obtained by the present invention is used for the above-mentioned construction use or civil engineering use, it is necessary to impart self-extinguishing property and flame retardancy to the foamed molded product. . In order to impart self-extinguishing property and flame retardancy to the regenerated foam molded article, the surface of the foamed resin particles may be subjected to a covering treatment by adding a flame retardant or, if necessary, a flame retardant aid, and then foam molding. . As the flame retardant, brominated alicyclic compounds, brominated aromatic compounds, brominated aromatic polymers, brominated phenyl (meth) acrylic acid esters and the like are preferably used. If the above flame retardant is in powder form, JIS standard sieve 149μ
It is desirable to use fine powder of m-passage in terms of adhesion to the particle surface. Further, in order to ensure adhesion to particles, a powdery flame retardant may be coated and spread after being partially coated with a liquid flame retardant having an appropriate viscosity. Further, a powdery flame retardant having a relatively low melting point may be heated and dissolved to perform coating treatment. Specific examples of such a flame retardant bring about self-extinguishing property by using a relatively small amount, good adhesion to the surface of the expanded resin particles, does not inhibit fusion between the expanded particles during molding, and has weather resistance. Well, it does not deteriorate the resin substrate. Ether and the like are particularly preferably used. These flame retardants are used in the range of 0.5 to 2.0% by weight, more preferably 0.8 to 1.5% by weight, based on the expanded resin particles. In addition, 0.1 to 0.5% by weight of a compound having an O—O, C—C, N═N bond, such as an organic peroxide, as a flame retardant aid.
You may use it together with the flame retardant. Examples of preferred flame retardant aids include dicumyl peroxide, 1,1-diphenylbicyclohexyl, azodiisobutyronitrile and the like.

【0032】また本発明の発泡樹脂粒子には、成形型へ
の充填性を改善する滑剤、成形時の融着促進剤、成形冷
却時間短縮剤、帯電防止剤、着色剤等の表面処理剤を被
覆してもよい。具体的には、エチレンビスステアロアミ
ド、高級脂肪酸、高級脂肪酸アミド、食用油、高級脂肪
酸トリグリセライド、高級脂肪酸モノグリセライド、パ
ラフィンワックス、ポリエチレンワックス、ジンクステ
アレート等を挙げることができる。
Further, the foamed resin particles of the present invention include a surface-treating agent such as a lubricant for improving the filling property in a molding die, a fusion promoter during molding, a molding cooling time shortening agent, an antistatic agent, a colorant and the like. You may coat. Specifically, ethylene bis stearamide, higher fatty acid, higher fatty acid amide, edible oil, higher fatty acid triglyceride, higher fatty acid monoglyceride, paraffin wax, polyethylene wax, zinc stearate and the like can be mentioned.

【0033】なお、このような表面被覆処理は、リボン
ブレンダー、タンブラー、レーディゲミキサー、ナウタ
ーミキサー、スーパーミキサー、ラインミキサー等を利
用して行われる。
Such surface coating treatment is carried out by using a ribbon blender, a tumbler, a Loedige mixer, a Nauta mixer, a super mixer, a line mixer or the like.

【0034】[0034]

【実施例】以下、本発明を実施例を用いて説明するが、
これにより本発明は限定されるものではなく、本発明の
範囲内で種々の変更が可能である。
EXAMPLES The present invention will be described below with reference to examples.
The present invention is not limited thereby, and various modifications can be made within the scope of the present invention.

【0035】家電製品の緩衝包装材として使用された発
泡性ポリスチレン樹脂粒子の発泡成形品を、破砕機で粒
子径約10〜20mmに破砕し、これを再生発泡成形体
の出発原料として用いた。この破砕した発泡樹脂粒子に
難燃性として、テトラブロモビスフェノールのビスアリ
ルエーテル1.2重量%を、スーパーミキサーを用いて
表面被覆処理した。この難燃剤を被覆した発泡粒子(カ
サ容積で5000ml)を容器6000mlの攪拌器付
きの容器に入れ、攪拌しながら加熱空気を容器の下部か
ら均等に吹き込み、所望のカサ容積まで発泡粒子を減容
化した。
A foam molded product of expandable polystyrene resin particles used as a cushioning packaging material for home electric appliances was crushed with a crusher to a particle diameter of about 10 to 20 mm, and this was used as a starting material for a recycled foam molded product. The crushed foamed resin particles were flame-retarded with 1.2% by weight of bisallyl ether of tetrabromobisphenol and surface-coated with a super mixer. The expanded particles coated with this flame retardant (5000 ml in bulk volume) were placed in a container with a stirrer of 6000 ml, and heated air was blown evenly from the bottom of the container while stirring to reduce the volume of the expanded particles to the desired bulk volume. Turned into

【0036】次いで、加圧状態に維持した、内寸が30
×30×2.5cmの型窩を有した成形型内に、上記の
減容化した発泡粒子を加圧空気を用いて圧縮充填した。
樹脂粒子の充填後、成形型の加圧状態を解除して、所定
温度の水蒸気を導入して加熱発泡することにより、再生
発泡成形体を製造した。
Then, the inner size was maintained at 30 while maintaining the pressure.
The volume-expanded foamed particles were compressed and filled in a molding die having a die cavity of x30 x 2.5 cm using pressurized air.
After the resin particles were filled, the pressurizing state of the molding die was released, and steam at a predetermined temperature was introduced to heat and foam to produce a regenerated foamed molded body.

【0037】減容化の処理条件、成形型内での成形条
件、及び得られた再生発泡成形体について表1に示す。
ビカット軟化点は、JIS K−7206(B法 5k
gf)に準拠して測定した。なお出発原料として用いた
廃発泡成形体は、一度使用した家電製品の緩衝包装材で
あって、実施例1、及び比較例1〜6は55倍発泡成形
品、実施例2は60倍発泡成形品、実施例3及び実施例
4は40倍発泡成形品である。また、これらの基材樹脂
は、ポリスチレンである。実施例5は、スチレン92%
と無水マレイン酸8%との共重合体の40倍発泡成形品
である。
Table 1 shows the processing conditions for volume reduction, the molding conditions in the molding die, and the regenerated foamed moldings obtained.
Vicat softening point is JIS K-7206 (B method 5k
It was measured according to gf). The waste foamed molding used as a starting material is a buffer packaging material for home appliances that has been used once. Example 1 and Comparative Examples 1 to 6 are 55 times foam molded articles, and Example 2 is 60 times foam molded. The products, Examples 3 and 4, are 40-fold foam molded products. Further, these base resins are polystyrene. Example 5 is 92% styrene
And a maleic anhydride 8% copolymer 40 times foam molded article.

【0038】実施例1〜5は何れも製造上支障はなく、
得られた再生発泡成形体は、均質で融着良好な高品質の
ものであった。得られた再生発泡成形体について、JI
SK−7201の酸素指数法による燃焼試験方法に準拠
して自消性を評価した結果、酸素指数26以上であり、
良好な難燃性を有していた。これに対し比較例1は、減
容化温度が高過ぎて、発泡樹脂粒子の減容化が急速とな
りすぎて不均一となった。比較例2は減容温度が低すぎ
て、減容に長時間を要し実施上不十分であった。比較例
3は、減容が不足して、得られた成形品は空間を残して
収縮した。比較例4は、成形型に充填するときの圧縮が
不足して得られた成形品は空間を残して収縮した。比較
例5は、成形時の熱不足で融着が不良となった。比較例
6は、成形時の熱過剰で収縮した。
In each of Examples 1 to 5, there was no problem in manufacturing,
The regenerated foamed molded product thus obtained was of high quality which was homogeneous and had good fusion bonding. Regarding the obtained regenerated foam molded article, JI
As a result of evaluating the self-extinguishing property according to the combustion test method by the oxygen index method of SK-7201, the oxygen index is 26 or more,
It had good flame retardancy. On the other hand, in Comparative Example 1, the volume reduction temperature was too high, and the volume reduction of the expanded resin particles became too rapid, resulting in non-uniformity. In Comparative Example 2, the volume reduction temperature was too low, and it took a long time to reduce the volume, which was insufficient in practice. In Comparative Example 3, the volume reduction was insufficient, and the obtained molded product contracted leaving a space. In Comparative Example 4, the molded product obtained due to insufficient compression when filled in the mold shrinks leaving a space. In Comparative Example 5, fusion was poor due to insufficient heat during molding. Comparative Example 6 contracted due to excessive heat during molding.

【0039】[0039]

【表1】 [Table 1]

【0040】[0040]

【発明の効果】本発明によれば、使用済みの発泡ポリス
チレン系樹脂成形体を破砕した発泡樹脂粒子を、加熱空
気で熱収縮させて減容化した後、成形型で発泡成形する
か、又は、さらに減容化した発泡粒子を圧縮した状態で
成形型内に充填し、加熱して発泡成形する。
According to the present invention, foamed resin particles obtained by crushing a used expanded polystyrene resin molded product are heat-shrinked with heated air to reduce the volume and then foam-molded with a molding die, or Then, the foamed particles, the volume of which is further reduced, are filled in a molding die in a compressed state and heated to foam-mold.

【0041】これにより、発泡粒子の正常な気泡をその
まま利用し、廃発泡成形体の減容化、リペレット、発泡
剤含浸、予備発泡、加熱成形という従来の煩雑な工程を
経ることなしに、しかも多くの熱エネルギーを消費する
ことなしに、容易に高品質の再生発泡成形体を製造する
ことができる。そして、本発明により得られた再生発泡
成形体は、建築用途、土木用途をはじめ、多くの分野に
利用可能である。
Thus, the normal bubbles of the expanded particles can be used as they are without the conventional complicated steps of reducing the volume of the waste expanded molded product, re-pelleting, impregnation of the foaming agent, pre-expanding, and heat molding. It is possible to easily produce a high-quality recycled foamed molded product without consuming a lot of heat energy. The regenerated foamed molded product obtained by the present invention can be used in many fields including construction and civil engineering.

【0042】さらに、本発明の再生発泡成形体の製造方
法は、大量に発生する使用済み発泡成形体を有効に再生
することができ、廃棄処理対策あるいは資源の有効利用
法として多大な効果が得られるという効果を奏する。
Further, the method for producing a regenerated foamed molded article of the present invention can effectively recycle a large amount of used foamed molded article, and has great effects as a disposal treatment measure or an effective use of resources. The effect of being able to be played.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】廃発泡ポリスチレン系樹脂成形体を破砕し
た発泡樹脂粒子を、元のカサ容積の75%以下になるよ
うに加熱空気を用いて熱収縮させて減容化した後、この
減容化した樹脂粒子を成形型内に供給し、基材樹脂のビ
カット軟化点よりも10〜40℃高い温度域の水蒸気を
導入して加熱することにより発泡成形体を得ることを特
徴とする再生発泡ポリスチレン系樹脂成形体の製造方
法。
1. The volume of foamed resin particles obtained by crushing a waste expanded polystyrene resin molded product is reduced by thermally shrinking the expanded resin particles with heated air so that the volume of the expanded resin particles becomes 75% or less of the original volume. Regenerated foaming, characterized in that a foamed molded body is obtained by supplying the resin particles thus converted into a molding die, introducing steam in a temperature range 10 to 40 ° C. higher than the Vicat softening point of the base resin, and heating the foamed molded body. A method for producing a polystyrene resin molded body.
【請求項2】加熱空気の温度が基材樹脂のビカット軟化
点よりも10〜60℃高い温度域であることを特徴とす
る請求項1記載の再生発泡ポリスチレン系樹脂成形体の
製造方法。
2. The method for producing a regenerated expanded polystyrene resin molded article according to claim 1, wherein the temperature of the heated air is in a temperature range higher by 10 to 60 ° C. than the Vicat softening point of the base resin.
【請求項3】減容化処理した樹脂粒子を、成形型内充填
後のカサ容積が元のカサ容積の80%以下になるように
加圧空気で圧縮して成形型内に供給することを特徴とす
る請求項1記載の再生発泡ポリスチレン系樹脂成形体の
製造方法。
3. The volume-reduced resin particles are compressed with pressurized air so that the bulk volume after filling the mold is 80% or less of the original bulk volume, and the resin particles are supplied into the mold. The method for producing a regenerated expanded polystyrene resin molded article according to claim 1.
JP4337554A 1992-12-17 1992-12-17 Method for producing recycled expanded polystyrene resin molded article Expired - Fee Related JP2798572B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4337554A JP2798572B2 (en) 1992-12-17 1992-12-17 Method for producing recycled expanded polystyrene resin molded article

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4337554A JP2798572B2 (en) 1992-12-17 1992-12-17 Method for producing recycled expanded polystyrene resin molded article

Publications (2)

Publication Number Publication Date
JPH06182891A true JPH06182891A (en) 1994-07-05
JP2798572B2 JP2798572B2 (en) 1998-09-17

Family

ID=18309743

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4337554A Expired - Fee Related JP2798572B2 (en) 1992-12-17 1992-12-17 Method for producing recycled expanded polystyrene resin molded article

Country Status (1)

Country Link
JP (1) JP2798572B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5687916A (en) * 1995-11-06 1997-11-18 Kimberly-Clark Worldwide, Inc. Method of nonwoven reclaim
US6066221A (en) * 1997-06-17 2000-05-23 Kimberly-Clark Worldwide, Inc. Method of using zoned hot air knife

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5687916A (en) * 1995-11-06 1997-11-18 Kimberly-Clark Worldwide, Inc. Method of nonwoven reclaim
US6066221A (en) * 1997-06-17 2000-05-23 Kimberly-Clark Worldwide, Inc. Method of using zoned hot air knife

Also Published As

Publication number Publication date
JP2798572B2 (en) 1998-09-17

Similar Documents

Publication Publication Date Title
KR101477124B1 (en) Expanded polystyrene resin particle and method of manufacture for same, polystyrene resin pre-expansion particle, polystyrene resin expanded form, thermoplastic resin pre-expansion particle and method of manufacture for same, and thermoplastic expanded form
JP5372783B2 (en) Expandable polystyrene resin particles, method for producing the same, and foam molded article
KR102010450B1 (en) Manufacturing method of a molded foam article with low density using propylene based polymer
JP5603629B2 (en) Method for producing thermoplastic resin pre-expanded particles, method for producing thermoplastic resin foam molding
JPH0598062A (en) Foamable styrene resin granule and production thereof
JP2007283576A (en) Manufacturing process of foamed polyolefinic resin molding utilizing compression volume-reduced waste foamed polyolefinic resin molding
JP2798572B2 (en) Method for producing recycled expanded polystyrene resin molded article
JP5603628B2 (en) Expandable polystyrene resin particles and method for producing the same, method for producing polystyrene resin pre-expanded particles, and method for producing polystyrene resin foam molded article
JP2007203559A (en) Manufacturing process of foamed polyolefin based resin molding using lump obtained from waste foamed polyolefin based resin molding
JPH07314438A (en) Production of foamable thermoplastic resin granule
JPH06298983A (en) Production of expandable thermoplastic resin particle
JP5425654B2 (en) Expandable polystyrene resin particles and method for producing the same, polystyrene resin pre-expanded particles, and polystyrene resin foam molded article
JP2637664B2 (en) Method for producing recycled expanded polystyrene resin molded article
JP2006116818A (en) Method for producing foamed polyolefin resin molding using waste foamed polyolefin resin molding and its molding
JP2005297464A (en) Manufacturing method for foamed polyolefin-based resin molding using waste foamed polyolefin-based resin molding
JP3981299B2 (en) Method for producing expandable particles from recovered styrene resin
JP5704831B2 (en) Bubble-containing expandable polystyrene resin particles and method for producing the same, polystyrene resin pre-expanded particles, and method for producing polystyrene resin foam molded article
JPH04325534A (en) Foamable polystyrene resin particle and its production
JP2012072230A (en) Expandable polystyrene-based resin particle and method for producing the same, polystyrene-based resin pre-expanded particle, and polystyrene-based resin expansion-molded article
JP2013072003A (en) Foamable polystyrene-based resin particles and method for producing the same, polystyrene-based resin prefoamed particles, and polystyrene-based resin foamed molding
JP4990814B2 (en) Process for producing modified polystyrene resin particles, pre-expanded particles, and expanded molded article.
JP2004115690A (en) Method for manufacturing expandable particle of styrene type resin
JP2004292489A (en) Styrenic resin expandable particle, method for producing the same, expanded particle and expansion molded product
JPH06145409A (en) Expandable styrene-based resin particle and its production
JP2013071998A (en) Foamable polystyrene-based resin particle, method for producing the same, polystyrene-based resin pre-foamed particle and polystyrene-based resin foamed compact

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees