JPH03247633A - Volatile foaming agent for expansion of thermoplastic resin - Google Patents

Volatile foaming agent for expansion of thermoplastic resin

Info

Publication number
JPH03247633A
JPH03247633A JP4241190A JP4241190A JPH03247633A JP H03247633 A JPH03247633 A JP H03247633A JP 4241190 A JP4241190 A JP 4241190A JP 4241190 A JP4241190 A JP 4241190A JP H03247633 A JPH03247633 A JP H03247633A
Authority
JP
Japan
Prior art keywords
foaming agent
thermoplastic resin
expansion
foaming
foam
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP4241190A
Other languages
Japanese (ja)
Inventor
Motosuke Ogawa
素右 小川
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.)
Chemours Mitsui Fluoroproducts Co Ltd
Original Assignee
Du Pont Mitsui Fluorochemicals 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 Du Pont Mitsui Fluorochemicals Co Ltd filed Critical Du Pont Mitsui Fluorochemicals Co Ltd
Priority to JP4241190A priority Critical patent/JPH03247633A/en
Publication of JPH03247633A publication Critical patent/JPH03247633A/en
Pending legal-status Critical Current

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  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

PURPOSE:To obtain the subject volatile foaming agent consisting of a chlorotetrafluoroethane, capable of providing an expanded material free from post-shrinkage or post-expansion after production, having a low danger of destruction of ozone layer and suitable for production of a thermoplastic resin expanded material. CONSTITUTION:A volatile foaming agent consisting of a chlorotetrafluoroethane (e.g. 1-chloro-1,2,2,2-tetrafluoroethane). Expansion is carried out by blending the above-mentioned foaming agent with a thermoplastic resin such as polyethylene or polypropylene.

Description

【発明の詳細な説明】 イ1発明の目的 [産業上の利用分野] 本発明はポリエチレン、ポリプロピレン、ポリブチレン
等の熱可塑性樹脂発泡体製造用の揮発性発泡剤に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION (1) Object of the Invention [Field of Industrial Application] The present invention relates to a volatile blowing agent for producing thermoplastic resin foams such as polyethylene, polypropylene, and polybutylene.

[従来の技術] 従来、熱可塑性樹脂の発泡において、特にポリエチレン
のようなポリオレフィンの発泡では、押出発泡直後にフ
オームが収縮するという問題があった。
[Prior Art] Conventionally, in the foaming of thermoplastic resins, particularly in the foaming of polyolefins such as polyethylene, there has been a problem that the foam shrinks immediately after extrusion foaming.

これは使用した樹脂に対する発泡剤と空気の透過速度の
違いに原因があり、発泡剤は速やかにフオーム(セル)
内部より外界に透過してしまうのに、空気はゆるやかに
セル内に入り込むためである。従って押出発泡径寸法の
回復をはかる為に長時間エージングしなければならない
という問題があった。
This is due to the difference in the permeation speed of the blowing agent and air to the resin used, and the blowing agent quickly forms (cells).
This is because air enters the cell slowly, even though it passes from the inside to the outside world. Therefore, there was a problem in that aging had to be carried out for a long time in order to recover the diameter of the extruded foam.

揮発性発泡剤としてはフロン114が比較的空気の透過
速度に近い為貰用されてきたが、この問題を完全には解
決できていない。
Freon 114 has been used as a volatile foaming agent because its permeation rate is relatively close to that of air, but this problem has not been completely solved.

また、前記フロン114を含め、CFC(クロロフルオ
ロカーボン)は大気中で極めて安定であり分解されない
まま大気層上空のオゾン層にまで達して紫外線の作用で
分解され、その分解物がオゾン層を破壊する懸念がある
との問題も起こっているので、これらCFCに代えて、
オゾン層破壊の恐れの少ない発泡剤が望まれている。
In addition, CFCs (chlorofluorocarbons), including the above-mentioned Freon 114, are extremely stable in the atmosphere and reach the ozone layer above the atmosphere without being decomposed, where they are decomposed by the action of ultraviolet rays, and the decomposed products destroy the ozone layer. There are also concerns about concerns, so instead of these CFCs,
A blowing agent that is less likely to cause ozone layer depletion is desired.

[発明が解決しようとする課題] 本発明は、揮発性発泡剤を用いて熱可塑性樹脂発泡体を
製造するに際して収縮、膨張がほとんど起こらず、また
オゾン層に達する前に分解してしまいオゾン層破壊の恐
れが少ない発泡剤を提供することを目的とする。
[Problems to be Solved by the Invention] The present invention is characterized in that when a thermoplastic resin foam is manufactured using a volatile blowing agent, almost no contraction or expansion occurs, and the foam decomposes before reaching the ozone layer. The purpose of the present invention is to provide a foaming agent that is less likely to break.

口0発明の構成 [課題を解決するための手段] 本発明に係る熱可塑性樹脂発泡用揮発性発泡剤は、クロ
ロテトラフルオロエタンより成る。
Configuration of the Invention [Means for Solving the Problems] The volatile foaming agent for foaming thermoplastic resin according to the present invention is composed of chlorotetrafluoroethane.

クロロテトラフルオロエタンの代表例としては1−クロ
ロ−1,2,2,2−テトラフルオロエタン(以下、フ
ロン124と略称する)が挙げられる。
A typical example of chlorotetrafluoroethane is 1-chloro-1,2,2,2-tetrafluoroethane (hereinafter abbreviated as Freon 124).

フロン124は、特にポリオレフィンに対して透過度が
従来ポリオレフィンの発泡に使用されている発泡剤、例
えば、プロパン、ブタン、ペンタン、フロン11、フロ
ン12、フロン114等よりもかなり小さく、また、空
気の透過度とほぼ同一であることを発見した。
In particular, Freon 124 has a much lower permeability to polyolefins than blowing agents conventionally used for foaming polyolefins, such as propane, butane, pentane, Freon 11, Freon 12, Freon 114, etc. It was found that the transmittance was almost the same as the transmittance.

本発明の発泡剤が使用できる熱可塑性樹脂は、ポリオレ
フィン、即ちエチレン、プロピレン、ブテン等のオレフ
ィンの単独重合体、又はこれらの共重合体、或はこれら
のオレフィンを主体とする他のビニル単量体との共重合
体又はこれらの重合体の混合物等である。又ポリスチレ
ン及びポリスチレン混合体等においても同様に使用でき
る。
Thermoplastic resins that can be used with the blowing agent of the present invention include polyolefins, that is, homopolymers of olefins such as ethylene, propylene, and butene, or copolymers thereof, or other vinyl monomers mainly composed of these olefins. copolymers with polymers, or mixtures of these polymers. Also, polystyrene and polystyrene mixtures can be similarly used.

発泡方法は、従来行われている熱可塑性樹脂の発泡手段
を何ら変更することを必要としない。
The foaming method does not require any modification of conventional thermoplastic resin foaming means.

例えば、ポリオレフィンと核形成剤をよく混合し、これ
を押出機のホッパーから加熱された押出機内に供給し、
ポリオレフィンを溶融混和し、これに本発明の揮発性発
泡剤を圧入し、温度制御された口金から大気中に押出す
ことによって発泡体が得られる。
For example, a polyolefin and a nucleating agent are thoroughly mixed, and this is fed from an extruder hopper into a heated extruder,
A foam is obtained by melt-blending a polyolefin, pressurizing the volatile blowing agent of the present invention, and extruding it into the atmosphere through a temperature-controlled die.

発泡体の形状はシート状、棒状、その他任意の形状に押
し出す事が可能である。又この際用いられる核形成剤は
、無機微粉末、分解型発泡剤など従来使用されているも
のを用いることは何ら差し支えない。
The foam can be extruded into a sheet, rod, or any other desired shape. Further, the nucleating agent used at this time may be any conventionally used nucleating agent such as inorganic fine powder or decomposable foaming agent.

[作用] 本発明の発泡剤によって押し出された発泡体は押出直後
の収縮、膨張が殆どない。故に、発泡体のエージングが
殆ど不要であり、巻き取ったフオームの巻き戻し等の時
間と手数が簡略化できる。
[Function] The foam extruded by the foaming agent of the present invention hardly shrinks or expands immediately after extrusion. Therefore, aging of the foam is almost unnecessary, and the time and effort required for unwinding the wound foam can be simplified.

[試験例] 無架橋の低密度ポリエチレンフィルム(フィルム厚50
μ)に対するガス透過度をDr、 Lyssy式ガス・
水蒸気透過度測定装置で測定した。各ガスの測定を2回
ずつ行った結果の平均値及び空気の透過率を1.0とし
た時の倍率を第1表に示す。
[Test example] Non-crosslinked low density polyethylene film (film thickness 50
Dr, Lyssy gas permeability for μ)
Measured using a water vapor permeability measuring device. Table 1 shows the average value of the results of measuring each gas twice and the magnification when the air permeability is set to 1.0.

第1表に示されるように、フロン124は、その透過度
が空気とほぼ同一である。
As shown in Table 1, the permeability of Freon 124 is almost the same as that of air.

[実施例1] 無架橋の低密度ポリエチレン(MI値7.2、密度0.
917g/cm” 、融点106℃)100重量部に、
核形成剤としてタルクな0.3重量部加え、ブレンダー
でよ(混合した後、押出機ホッパーより供給した。供給
された押出機内でこの混合物は加熱溶融され、スクリュ
ーにより押出機中を前方に移動する。この時押出機中途
部分よりフロン124を120 k g / c m 
”の圧力にポンプにより昇圧して押出機中に圧入し、溶
融樹脂に充分混合した。この発泡剤混合の溶融樹脂な押
出機先端の110℃に温度制御された口金より押出して
厚さ2mmのシート状発泡体を得た。
[Example 1] Non-crosslinked low density polyethylene (MI value 7.2, density 0.
917 g/cm", melting point 106°C) to 100 parts by weight,
Add 0.3 parts by weight of talc as a nucleating agent and mix in a blender (after mixing, the mixture was fed from the extruder hopper. The mixture was heated and melted in the supplied extruder, and moved forward in the extruder by a screw. At this time, 120 kg/cm of Freon 124 was added from the middle part of the extruder.
This molten resin mixed with a foaming agent was extruded through a nozzle at the tip of the extruder whose temperature was controlled at 110°C to a thickness of 2 mm. A sheet-like foam was obtained.

この発泡体は約30倍の発泡倍率を持ち、気泡は均一微
細であり、10100mmX100の正方形に切り出し
たところ、発泡直後の大きさから殆ど変化はなかった。
This foam had a foaming ratio of about 30 times, the cells were uniform and fine, and when cut into a 10100 mm x 100 square, there was almost no change in the size from the size immediately after foaming.

C比較例1〕 実施例で使用したフロン124の代わりにフロン114
を使用して発泡体を得た。使用条件、使用機器、押し出
し条件等はすべて実施例と同様とした。発泡直後の大き
さから収縮そして膨張が認められた。
C Comparative Example 1] Freon 114 was used instead of Freon 124 used in the example.
The foam was obtained using The conditions of use, equipment used, extrusion conditions, etc. were all the same as in the examples. Shrinkage and expansion were observed from the size immediately after foaming.

実施例1及び比較例1により製造された発泡体の観察結
果を第2表に示す。
Table 2 shows the observation results of the foams produced in Example 1 and Comparative Example 1.

第2表 注:すべでの発泡体は24℃で寸法測定及び保存された
Table 2 Note: All foams were sized and stored at 24°C.

フロン124はフロン114より発泡体の寸法安定性に
優れている。
Freon 124 has better dimensional stability of the foam than Freon 114.

ハ 発明の効果 本発明の発泡剤を使用すると、製造後収縮、膨張が殆ど
起こらない熱可塑性樹脂発泡体を製造できる。故に発泡
体の熟成工程が不要であり、熟成の為に貯蔵庫に保管す
ることや巻とったシートなどの巻戻しなどの時間と手数
が簡略化できる。
C. Effects of the Invention By using the blowing agent of the present invention, it is possible to produce thermoplastic resin foams that undergo almost no shrinkage or expansion after production. Therefore, there is no need for a foam aging process, and the time and effort required for storing the foam in a storage for aging and unwinding the rolled sheet can be simplified.

また、本発明におけるクロロテトラフルオロエタンは水
素原子を含む化合物であることにより、オゾン層に達す
る前に分解すると推定され、オゾン破壊の恐れが少ない
と考えられる。
Further, since chlorotetrafluoroethane in the present invention is a compound containing a hydrogen atom, it is estimated that it decomposes before reaching the ozone layer, and is considered to have little risk of ozone destruction.

Claims (1)

【特許請求の範囲】 1 クロロテトラフルオロエタンより成る熱可塑性樹脂
発泡用揮発性発泡剤。 2 クロロテトラフルオロエタンが1−クロロ−1,2
,2,2−テトラフルオロエタンである請求項第1項記
載の熱可塑性樹脂発泡用揮発性発泡剤。
[Claims] 1. A volatile foaming agent for foaming thermoplastic resins comprising chlorotetrafluoroethane. 2 Chlorotetrafluoroethane is 1-chloro-1,2
, 2,2-tetrafluoroethane. The volatile foaming agent for thermoplastic resin foaming according to claim 1, which is 2,2-tetrafluoroethane.
JP4241190A 1990-02-26 1990-02-26 Volatile foaming agent for expansion of thermoplastic resin Pending JPH03247633A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4241190A JPH03247633A (en) 1990-02-26 1990-02-26 Volatile foaming agent for expansion of thermoplastic resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4241190A JPH03247633A (en) 1990-02-26 1990-02-26 Volatile foaming agent for expansion of thermoplastic resin

Publications (1)

Publication Number Publication Date
JPH03247633A true JPH03247633A (en) 1991-11-05

Family

ID=12635327

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4241190A Pending JPH03247633A (en) 1990-02-26 1990-02-26 Volatile foaming agent for expansion of thermoplastic resin

Country Status (1)

Country Link
JP (1) JPH03247633A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006185360A (en) * 2004-12-28 2006-07-13 Sony Computer Entertainment Inc Program debugging device, program debugging method, and program

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006185360A (en) * 2004-12-28 2006-07-13 Sony Computer Entertainment Inc Program debugging device, program debugging method, and program

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