JPS59227426A - Preparation of expanded thermoplastic resin article - Google Patents

Preparation of expanded thermoplastic resin article

Info

Publication number
JPS59227426A
JPS59227426A JP58102854A JP10285483A JPS59227426A JP S59227426 A JPS59227426 A JP S59227426A JP 58102854 A JP58102854 A JP 58102854A JP 10285483 A JP10285483 A JP 10285483A JP S59227426 A JPS59227426 A JP S59227426A
Authority
JP
Japan
Prior art keywords
thermoplastic resin
vacuum chamber
expanded
blowing agent
volatile blowing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP58102854A
Other languages
Japanese (ja)
Inventor
Masato Kubota
久保田 正登
Eiji Saito
英二 斉藤
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.)
Idemitsu Petrochemical Co Ltd
Original Assignee
Idemitsu Petrochemical 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 Idemitsu Petrochemical Co Ltd filed Critical Idemitsu Petrochemical Co Ltd
Priority to JP58102854A priority Critical patent/JPS59227426A/en
Publication of JPS59227426A publication Critical patent/JPS59227426A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/36Feeding the material to be shaped
    • B29C44/46Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length
    • B29C44/50Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying
    • B29C44/507Feeding the material to be shaped into an open space or onto moving surfaces, i.e. to make articles of indefinite length using pressure difference, e.g. by extrusion or by spraying extruding the compound through an annular die
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion 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
    • B29C48/09Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels
    • B29C48/10Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels flexible, e.g. blown foils
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/91Heating, e.g. for cross linking
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/911Cooling
    • B29C48/9135Cooling of flat articles, e.g. using specially adapted supporting means
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/919Thermal treatment of the stream of extruded material, e.g. cooling using a bath, e.g. extruding into an open bath to coagulate or cool the material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001Combinations of extrusion moulding with other shaping operations
    • B29C48/0018Combinations of extrusion moulding with other shaping operations combined with shaping by orienting, stretching or shrinking, e.g. film blowing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001Combinations of extrusion moulding with other shaping operations
    • B29C48/0019Combinations of extrusion moulding with other shaping operations combined with shaping by flattening, folding or bending

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)

Abstract

PURPOSE:To make it possible to efficiently recover a volatile blowing agent, by a method wherein a volatile blowing agent-containing thermoplastic resin is extruded into a vacuum chamber from a die to be expanded while the expanded resin is introduced into a water tank constituted so as to hermetically close the outlet of the vacuum chamber. CONSTITUTION:A resin 1 is extruded into a vacuum chamber 3 from a die 2 to be expanded. In this case, the pressure of the vacuum chamber 3 is usually set to atmospheric pressure or less, pref., 60-760mm.Hg (absolute pressure). In addition, the recovery rate of a volatile blowing agent can be enhanced by heating the vacuum chamber 3 by a heating apparatus 4. Thus obtained expanded thermoplastic resin article 5 is introduced into a water tank 6 constituted so as to hermetically close the outlet of the vacuum chamber 3 while the cooled expanded thermoplastic resin article 5 is continuously taken up in the atomosphere by a take-up roll 7. Even if this take-up speed is extremely accelerated to the max. 100-150m/min and high speed molding is performed, an excellent expanded article can be obtained.

Description

【発明の詳細な説明】 本発明は熱可塑性樹脂発泡体の製造法に関し、詳しくは
揮発性発泡剤を効率よく回収しうるとともに、すぐれた
特性を有する熱可塑性樹脂発泡体を連続的に高速で製造
することができる熱可塑性樹脂発泡体の製造法に関する
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a thermoplastic resin foam, and more specifically, a method for efficiently recovering a volatile blowing agent and continuously producing a thermoplastic resin foam having excellent properties at high speed. The present invention relates to a method for producing a thermoplastic resin foam that can be produced.

一般に熱可塑性樹脂発泡体は、脂肪族炭化水素。Thermoplastic resin foams are generally made of aliphatic hydrocarbons.

弗化塩化炭化水素、アルコール類などの揮発性発泡剤を
含有する樹脂溶融物を押出グイより押出成形することに
より得られている。特に発泡倍率の高い発泡体を製造す
る場合には、多量の揮発性発泡剤が使用されている。こ
れらの揮発性発泡剤はダイから押出された後1気泡形成
に寄与するとともに1直接樹脂中から大気中に逃散する
ものもある。また、気泡形成に寄与した揮発性発泡剤も
二次的に気泡膜を透過して大気中に逃散する。これら大
気中に逃散する揮発性発泡剤ガスは、作業環境を悪化さ
せるばかりが、衛生面や安全面での問題もあり1効率的
な回収が望まれている。しかも、高発泡倍率の発泡体に
あっては、発泡体製造に占める発泡剤のコストも無視で
きないものであった。
It is obtained by extrusion molding a resin melt containing a volatile blowing agent such as a fluorinated chlorinated hydrocarbon or an alcohol using an extruder. In particular, when producing a foam with a high expansion ratio, a large amount of volatile blowing agent is used. These volatile blowing agents contribute to the formation of cells after being extruded from the die, and some of them directly escape from the resin into the atmosphere. In addition, the volatile blowing agent that contributed to the formation of the bubbles also secondarily passes through the bubble membrane and escapes into the atmosphere. These volatile blowing agent gases escaping into the atmosphere not only worsen the working environment, but also pose health and safety problems, so efficient recovery is desired. Furthermore, in the case of foams with high expansion ratios, the cost of the blowing agent that is involved in the production of the foam cannot be ignored.

本発明は上記従来の欠点を解消し、揮発性発泡剤を効率
よく回収しうるどともに、すぐれた特性を有する熱可塑
性樹脂発泡体を連続的に高速で製造することができる熱
可塑性樹脂発泡体の製造法を提供することを目的とする
ものである。
The present invention solves the above-mentioned conventional drawbacks, and provides a thermoplastic resin foam that can efficiently recover volatile blowing agents and produce thermoplastic resin foams having excellent properties continuously at high speed. The purpose of this invention is to provide a method for manufacturing.

すなわち本発明は、揮発性発泡剤含有熱可塑性樹脂をダ
イより減圧室に押出し発泡させた後、前記減圧室出口を
密閉するように構成した水槽に導入し、次いで引取ると
ともに、前記減圧室より揮発性発泡剤を回収することを
特徴とする熱可塑性樹脂発泡体の製造法を提供するもの
である。
That is, in the present invention, a thermoplastic resin containing a volatile foaming agent is extruded from a die into a vacuum chamber and foamed, and then introduced into a water tank configured to seal the outlet of the vacuum chamber, and then taken out and removed from the vacuum chamber. The present invention provides a method for producing a thermoplastic resin foam characterized by recovering a volatile blowing agent.

本発明の製造法に使用する熱可塑性樹脂としては特に制
限はなく様々なものが挙げられる。例えば、ポリエチレ
ン、ポリプロピレン等のポリオレフィン;エチレン、プ
ロピレンなどのオレフィンと他の共重合成分との共重合
体;ポリスチレン;スチレンと他の共重合成分との共重
合体;ポリ塩化ビニル;ポリアミド;ポリエステル;ポ
リアセタールなどあるいはこれらの混合物が挙げられる
The thermoplastic resin used in the production method of the present invention is not particularly limited, and various thermoplastic resins may be used. For example, polyolefins such as polyethylene and polypropylene; copolymers of olefins such as ethylene and propylene with other copolymer components; polystyrene; copolymers of styrene and other copolymer components; polyvinyl chloride; polyamide; polyester; Examples include polyacetal and mixtures thereof.

次に揮発性発泡剤としても特に制限はないが、例えば、
プロパン、ブタン、ペンタン、ヘキサン等の脂肪族炭化
水素;トリクロロモノフルオロメタン、ジクロロテトラ
フルオロエタン、ジクロロ等のアルコール類などあるい
はこれらの混合物が挙げられる。
Next, there are no particular restrictions on volatile foaming agents, but for example,
Examples include aliphatic hydrocarbons such as propane, butane, pentane, and hexane; alcohols such as trichloromonofluoromethane, dichlorotetrafluoroethane, and dichloro, and mixtures thereof.

上記熱可塑性樹脂と揮発性発泡剤との配合割合は、前者
100重量部に対し、通常後者5〜200重量部%好ま
しくは50〜150重量部である。
The blending ratio of the thermoplastic resin and the volatile foaming agent is usually 5 to 200 parts by weight, preferably 50 to 150 parts by weight, per 100 parts by weight of the former.

さらに、本発明においては必要によりメルク。Furthermore, in the present invention, Merck may be used as necessary.

クレー、シリカ等の気泡核形成剤を適宜加えることもで
きる。この気泡核形成剤の添加量は通常熱可塑性樹脂1
00重量部に対し、5重量部以下である0気泡核形成剤
の使用により、気泡を均一にすることができるとともに
気泡径を小さくすることができ、揮発性発泡剤を有効に
利用することができる。
A cell nucleating agent such as clay or silica can also be added as appropriate. The amount of this bubble nucleating agent added is usually 1 part of the thermoplastic resin.
By using the 0-cell nucleating agent in an amount of 5 parts by weight or less per 00 parts by weight, the bubbles can be made uniform and the cell diameter can be reduced, making it possible to effectively utilize the volatile blowing agent. can.

また、熱可塑性樹脂には必要により各種安定剤(酸化、
熱、光など)、充填材(炭酸カルシウム。
In addition, various stabilizers (oxidation,
heat, light, etc.), fillers (calcium carbonate.

メルク、クレー、カーボンブラックなど)、ゴム類、帯
電防止剤、可塑剤1着色剤などを適宜加えることができ
る。
Merck, clay, carbon black, etc.), rubbers, antistatic agents, plasticizers, colorants, etc. can be added as appropriate.

次に、本発明の製造法を図面に基いて説明する。Next, the manufacturing method of the present invention will be explained based on the drawings.

第1図は本発明の製造法に使用する装置の1例を示す概
略図である。
FIG. 1 is a schematic diagram showing an example of an apparatus used in the manufacturing method of the present invention.

まず、押出成形機等の成形機を用いて溶融した熱可塑性
樹脂に各種添加剤を加え、さらに揮発性発泡剤を加える
。ここてJ’iI:発性発泡剤は通常10〜200 k
mm”の圧力で熱可塑性樹脂中に圧入することが望まし
い。
First, various additives are added to a melted thermoplastic resin using a molding machine such as an extrusion molding machine, and then a volatile foaming agent is added. J'iI: The foaming agent is usually 10 to 200 k
It is preferable to press fit into the thermoplastic resin at a pressure of 100 mm.

次に、上記の溶融した揮発性発泡剤含有熱可塑性樹脂1
は十分に混紳しながら、樹脂の融点または軟化点に対し
て、−45℃〜+10℃程度に冷却する。
Next, the above melted volatile blowing agent-containing thermoplastic resin 1
While sufficiently mixing, the resin is cooled to about -45°C to +10°C relative to the melting point or softening point of the resin.

次いで、該拘脂1をダイ2より減圧室3に押出し発泡さ
せる。ここで減圧室3の圧力は熱可塑性樹脂や揮発性発
泡剤の種類等により異なり一義的に決定することは困丹
であるが、通常大気圧以下とする。好ましくは60 m
m1lji (絶対圧)から760mmB、9 (絶対
圧)とする。また、減圧室3は加熱装置4により加熱す
ることが好ましい。この加熱温度も熱可塑性樹脂や揮発
性発泡剤の種類等により異なり、一義的に決定すること
は困難であるが、常温から樹脂の融点または軟化点より
も10℃低い温度、通常50〜150℃である。加熱装
置4としてはヒーター等の既知の装置を使用することが
できる。減圧室3を加熱することにより、揮発性発泡剤
の回収率をより向上せしめることができる。
Next, the resin 1 is extruded from the die 2 into the vacuum chamber 3 and foamed. Here, the pressure in the decompression chamber 3 varies depending on the type of thermoplastic resin, volatile foaming agent, etc., and is difficult to determine unambiguously, but is usually set to below atmospheric pressure. Preferably 60 m
m1lji (absolute pressure) to 760 mmB, 9 (absolute pressure). Further, it is preferable that the decompression chamber 3 be heated by a heating device 4 . This heating temperature also varies depending on the type of thermoplastic resin and volatile blowing agent, and is difficult to determine unambiguously, but it ranges from room temperature to a temperature 10 degrees Celsius lower than the melting point or softening point of the resin, usually 50 to 150 degrees Celsius. It is. As the heating device 4, a known device such as a heater can be used. By heating the vacuum chamber 3, the recovery rate of the volatile foaming agent can be further improved.

なお、ダイ2の形式としてはフラットダイ式あるいはザ
ーキュラーダイ式のいずれをも使用することができる。
In addition, as the format of the die 2, either a flat die type or a circular die type can be used.

フラットダイ式を使用することによりフィルム状あるい
はシート状の熱可塑性樹脂発泡体を製造することができ
、またサーキュラ−ダイ式を使用することにより筒状の
熱可塑性樹脂発泡体を製造することができる。
By using the flat die method, it is possible to produce film- or sheet-shaped thermoplastic resin foams, and by using the circular die method, it is possible to produce cylindrical thermoplastic resin foams. .

このようにして得られた熱可塑性樹脂発泡体5を、減圧
室3出口を密閉するように構成した水槽6に導入する。
The thermoplastic resin foam 5 thus obtained is introduced into a water tank 6 configured to seal the outlet of the vacuum chamber 3.

ここで該水槽6としては、減圧室3出日を密閉するよう
に、すなわち減圧室3と外気との通気を遮断しつる借造
のものであればよく特に制限はない。該水槽6に導入す
ることにより、熱可塑性樹脂発泡体5は冷却される。
Here, the water tank 6 is not particularly limited as long as it is a borrowed one that seals the decompression chamber 3, that is, blocks ventilation between the decompression chamber 3 and the outside air. By introducing the thermoplastic resin foam into the water tank 6, the thermoplastic resin foam 5 is cooled.

次いで、該水槽6に導入して冷却された熱可塑性樹脂発
泡体5を引取ロール7等により大気中に連続的に引取る
。なお、該発泡体5の引取速度は最高100〜150 
m/minと非常に高速成形してもすぐれた発泡体を得
ることが可能である。
Next, the thermoplastic resin foam 5 introduced into the water tank 6 and cooled is continuously taken up into the atmosphere by a take-up roll 7 or the like. In addition, the maximum take-up speed of the foam 5 is 100 to 150
It is possible to obtain an excellent foam even when molding is performed at a very high speed of m/min.

さらに、本発明の製造法においては、減圧ポンプ等の回
収装置8をt打いて、減圧室3よりガス状の揮発性発泡
剤を回収することが必要である。ここで該揮発性発泡剤
の回収方式としては特に制限はなく、凝縮式、吸着式あ
るいは吸収式のいずれをも使用することができる。
Furthermore, in the manufacturing method of the present invention, it is necessary to recover the gaseous volatile foaming agent from the vacuum chamber 3 by turning on a recovery device 8 such as a vacuum pump. There is no particular restriction on the recovery method for the volatile blowing agent, and any of the condensation type, adsorption type, and absorption type can be used.

このようにして回収された揮発性発泡剤を用いて上記操
作を繰返すことにより、熱可塑性樹脂発泡体を製造する
ことができる。
By repeating the above operation using the volatile foaming agent thus recovered, a thermoplastic resin foam can be manufactured.

以上説明したように、本発明の製造法においては溶融し
た揮発性発泡剤含有熱可塑性樹脂をダイより減圧室に押
出し発泡させた後、前記減圧室出口を密閉するように構
成した水槽に導入しており、減圧室内は大気中とは遮断
されて密閉状態とされている。本発明では、このような
減圧室より一度使用された揮発性発泡剤を回収し、揮発
性発泡剤を再使用するので発泡体の製造コストを低減化
することかできる。
As explained above, in the manufacturing method of the present invention, a molten thermoplastic resin containing a volatile blowing agent is extruded from a die into a vacuum chamber and foamed, and then introduced into a water tank configured to seal the outlet of the vacuum chamber. The inside of the decompression chamber is sealed off from the atmosphere. In the present invention, the once-used volatile foaming agent is recovered from such a vacuum chamber and the volatile foaming agent is reused, so that the manufacturing cost of the foam can be reduced.

しかも、上記の如く減圧室が密閉系とされているため1
揮発性発泡剤を効率よく回収することができるとともに
、回収時間を短縮化することができ、発泡体の連続高速
成形が可能である◇それ故・本発明の製造法は経済性に
すぐれたものである。
Moreover, as mentioned above, since the decompression chamber is a closed system, 1
The volatile foaming agent can be efficiently recovered, the recovery time can be shortened, and the foam can be continuously molded at high speed. Therefore, the production method of the present invention is highly economical. It is.

さらに揮発性発泡剤として可燃性ガスや有害ガスを発生
する発泡剤を使用することもでき)しがもこれら発泡剤
を用いても他の工程における作業環境を悪化させること
がない。
Further, as a volatile blowing agent, a blowing agent that generates flammable gas or harmful gas can also be used. However, even if these blowing agents are used, the working environment in other processes will not be deteriorated.

また1水槽により減圧室と大気との遮断とS5?3泡体
の冷却を併せて行なうことができるので、他に冷却手段
が不要となる。
Further, since one water tank can simultaneously isolate the decompression chamber from the atmosphere and cool the S5-3 foam, no other cooling means is required.

しかも、溶融した揮発性発泡剤含有熱可塑性樹脂をダイ
より減圧室に押出し発泡させているので、すぐれた特性
を有する発泡体が得られる。
Moreover, since the molten thermoplastic resin containing a volatile blowing agent is extruded from a die into a vacuum chamber and foamed, a foam having excellent properties can be obtained.

したがって、本発明の製造法はn袋材料や断熱材料等と
して用いる熱可塑性樹脂発泡体の製造に有効に利用する
ことができる。
Therefore, the manufacturing method of the present invention can be effectively utilized for manufacturing thermoplastic resin foams used as n-bag materials, heat insulating materials, and the like.

次に、本発明の実施例を示す。Next, examples of the present invention will be shown.

実施例1 第1図に示す装置を用いて熱可塑性樹脂発泡体の製造を
以下の方法により行なった。
Example 1 A thermoplastic resin foam was manufactured by the following method using the apparatus shown in FIG.

押出成形機を用いて200℃に溶融したポリプロピレン
(密度0.91.!iI/crn3.メルトインデック
ス(MI) 0.6 jl/10分)100爪遺部に対
して、トリクOoモノフルオpメタン81重量部および
ジクロロテトラフルオロエタン9 市j1 部ヲ150
 kW/an2で圧入し1十分に混練しつつ145 ”
C;に冷却し均一なものとした。次いで、この溶融した
揮発性発泡剤含有熱可塑↑1:、樹脂1乞ザーキュラー
ダイ2(ダイス径30mmψ)より減圧室3 (+−E
力630mm′R(絶対圧))へ押し出すとともに、ダ
イのエヤー供給口から加圧空気をバブル内部に供給し、
バブル径200mmの筒状の発泡体5を得た。この筒状
の発泡体5をピンチロール9を介して減圧室3より水槽
6に導入し、次いで引取ローA/7により大気中へ連続
的に引取った。なお、減圧室3は温度を100”Cとし
、減圧ポンプ(回収装置8)により減圧室内のガス状の
rjlj )A性発泡剤を回収した。
Polypropylene (density 0.91.!iI/crn3. Melt index (MI) 0.6 jl/10 min) melted at 200°C using an extrusion molding machine was used for 100 nail parts, TrikuOo monofluoropmethane 81 Parts by weight and dichlorotetrafluoroethane 9 parts 150
145" while press-fitting at kW/an2 and thoroughly kneading.
C; to make it uniform. Next, this melted volatile foaming agent-containing thermoplastic ↑1:, resin 1 is poured into a vacuum chamber 3 (+-E
At the same time, pressurized air is supplied to the inside of the bubble from the air supply port of the die.
A cylindrical foam 5 with a bubble diameter of 200 mm was obtained. This cylindrical foam 5 was introduced into the water tank 6 from the vacuum chamber 3 via the pinch rolls 9, and then continuously drawn into the atmosphere by the drawing row A/7. The temperature of the vacuum chamber 3 was set to 100''C, and the gaseous rjlj )A foaming agent in the vacuum chamber was recovered by a vacuum pump (recovery device 8).

運転開始50分後の定常状態における筒状の発泡体5の
減圧室滞留時間は20秒であり、ガスクロマトグラフで
測定した揮発性発泡剤の回収率は、トリクロロモノフル
オロメタン82%、ジクロロテトラフルオロエタン60
%であった。
The residence time of the cylindrical foam 5 in the vacuum chamber in a steady state 50 minutes after the start of operation was 20 seconds, and the recovery rate of the volatile blowing agent measured by gas chromatography was 82% for trichloromonofluoromethane and 82% for dichlorotetrafluoromethane. ethane 60
%Met.

実施例2 実施例1において、減圧室の条件を湯度115℃、圧力
630 mnl1jj (絶対圧)としたこと以外は、
実施例1に準じて行ない発泡体を得た。
Example 2 In Example 1, except that the conditions of the decompression chamber were 115°C hot water temperature and 630 mnl1jj (absolute pressure),
A foam was obtained in accordance with Example 1.

定常状態の揮発性発泡剤の回収率はトリクロロモノフル
オロメタン90%、ジクロロテトラフルオロエタン68
%であった。
Steady state volatile blowing agent recoveries were 90% for trichloromonofluoromethane and 68% for dichlorotetrafluoroethane.
%Met.

実施例3 実施例1において、減圧室の条件を温度60℃。Example 3 In Example 1, the temperature of the vacuum chamber was 60°C.

圧力630 tnrnN (絶対圧)としたこと以外は
、実施例1に準じて行ない発泡体を得た。
A foam was obtained in the same manner as in Example 1, except that the pressure was 630 tnrnN (absolute pressure).

定常状態の揮発性発泡剤の回収率はトリクロロモノフル
オロメタン60%、ジクロロテトラフルオロエタン31
%であった。
Steady state volatile blowing agent recoveries were 60% for trichloromonofluoromethane and 31% for dichlorotetrafluoroethane.
%Met.

【図面の簡単な説明】[Brief explanation of the drawing]

第】図は本発明の製造法に使用する装置の1例を示す概
略図である。 1・・・揮発性発泡剤含有熱可塑性樹脂。 2・・・ダイ、  3・・・減圧室、4・・・加熱装置
。 5・・・熱可塑性樹脂発泡体、  6°°°水槽・7・
・・引取ロール、 8・・・回収装置。 9・・・ピンチロール 特許出願人 出光石油化学株式会社
FIG. 1 is a schematic diagram showing an example of an apparatus used in the manufacturing method of the present invention. 1... Thermoplastic resin containing volatile foaming agent. 2...Die, 3...Decompression chamber, 4...Heating device. 5...Thermoplastic resin foam, 6°°°water tank, 7.
...Take-up roll, 8...Recovery device. 9... Pinch roll patent applicant Idemitsu Petrochemical Co., Ltd.

Claims (1)

【特許請求の範囲】 1、揮発性発泡剤含有熱可塑性樹脂をグイより減圧室に
押出し発泡させた後、前記減IEE室出口を密閉するよ
うに杓成した水槽に導入し、次いでづ[取るとともに、
前記減圧室より揮発性発泡剤を回収することを特徴とす
る熱可塑性樹脂発泡体の製造法。 2減圧室が50℃以上に加熱されている特許請求の範囲
第1項記載の製造法。
[Claims] 1. After extruding a thermoplastic resin containing a volatile foaming agent into a vacuum chamber and foaming it, the resin is introduced into a ladle-formed water tank so as to seal the outlet of the vacuum chamber, and then With,
A method for producing a thermoplastic resin foam, comprising recovering a volatile foaming agent from the vacuum chamber. 2. The manufacturing method according to claim 1, wherein the reduced pressure chamber is heated to 50° C. or higher.
JP58102854A 1983-06-10 1983-06-10 Preparation of expanded thermoplastic resin article Pending JPS59227426A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58102854A JPS59227426A (en) 1983-06-10 1983-06-10 Preparation of expanded thermoplastic resin article

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58102854A JPS59227426A (en) 1983-06-10 1983-06-10 Preparation of expanded thermoplastic resin article

Publications (1)

Publication Number Publication Date
JPS59227426A true JPS59227426A (en) 1984-12-20

Family

ID=14338509

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58102854A Pending JPS59227426A (en) 1983-06-10 1983-06-10 Preparation of expanded thermoplastic resin article

Country Status (1)

Country Link
JP (1) JPS59227426A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61101539A (en) * 1984-10-23 1986-05-20 Kanegafuchi Chem Ind Co Ltd Recovery of volatile blowing agent from pre-expanded polyolefin resin particle
JPH04325534A (en) * 1991-04-25 1992-11-13 Sekisui Plastics Co Ltd Foamable polystyrene resin particle and its production

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61101539A (en) * 1984-10-23 1986-05-20 Kanegafuchi Chem Ind Co Ltd Recovery of volatile blowing agent from pre-expanded polyolefin resin particle
JPH0513173B2 (en) * 1984-10-23 1993-02-19 Kanegafuchi Chemical Ind
JPH04325534A (en) * 1991-04-25 1992-11-13 Sekisui Plastics Co Ltd Foamable polystyrene resin particle and its production

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