JPH0812798A - Polyolefin resin prefoamed particle with antistatic property and its manufacture - Google Patents

Polyolefin resin prefoamed particle with antistatic property and its manufacture

Info

Publication number
JPH0812798A
JPH0812798A JP14617194A JP14617194A JPH0812798A JP H0812798 A JPH0812798 A JP H0812798A JP 14617194 A JP14617194 A JP 14617194A JP 14617194 A JP14617194 A JP 14617194A JP H0812798 A JPH0812798 A JP H0812798A
Authority
JP
Japan
Prior art keywords
polyolefin resin
particles
parts
weight
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
JP14617194A
Other languages
Japanese (ja)
Other versions
JP3456758B2 (en
Inventor
Tadayuki Ichimura
忠行 市村
Toshiaki Matsumoto
利章 松本
Kenichi Senda
健一 千田
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.)
Kanegafuchi Chemical Industry Co Ltd
Original Assignee
Kanegafuchi Chemical Industry 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 Kanegafuchi Chemical Industry Co Ltd filed Critical Kanegafuchi Chemical Industry Co Ltd
Priority to JP14617194A priority Critical patent/JP3456758B2/en
Publication of JPH0812798A publication Critical patent/JPH0812798A/en
Application granted granted Critical
Publication of JP3456758B2 publication Critical patent/JP3456758B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain polyolefin resin prefoamed particles that give foamed products having excellent surface properties and antistatic properties and good expandability and fusibility by mixing a specific antistatic agent with a polyolefin resin. CONSTITUTION:The polyolefin resin prefoamed particles are made of a polyolefin resin composition prepared by mixing 100 pts.wt. polyolefin resin and 0.05 to 5 pts.wt. hydroxyalkylmonoethanolamine represented by the formula wherein R is an 8-22 C alkyl group. preferably, the particles of the polyolefin resin composition further contains 0.005 to 0.1 pt.wt. organic pigment per 100 pts.wt. polyolefin resin.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は帯電防止性を有するポリ
オレフィン系樹脂予備発泡粒子およびその製法に関す
る。さらに詳しくは、ビーズ発泡性、融着性が良好で、
成形品の表面性、帯電防止性が良好で、黄変を起こさな
い型内発泡成形品を提供することができるポリオレフィ
ン系樹脂予備発泡粒子およびその製法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to pre-expanded polyolefin resin particles having antistatic properties and a method for producing the same. More specifically, beads have good foaming properties and fusion properties,
TECHNICAL FIELD The present invention relates to a polyolefin resin pre-expanded particle which has good surface properties and antistatic properties and can provide an in-mold expanded molded article that does not cause yellowing, and a method for producing the same.

【0002】[0002]

【従来の技術】ポリオレフィン系樹脂予備発泡粒子の型
内発泡成形品は、OA機器などの電子機器部品や一般機
器部品などの緩衝包装材として利用されているが、この
種の緩衝包装材は帯電しやすく、ほこりや静電気を嫌う
電子機器部品の包装材の用途には適さない。このため、
帯電防止性を有するポリオレフィン系樹脂予備発泡粒子
からなる型内発泡成形品が開発され始めている。
2. Description of the Related Art In-mold foam molded articles of polyolefin resin pre-expanded particles are used as cushioning packaging materials for electronic equipment parts such as office automation equipment and general equipment parts. It is not suitable for use as a packaging material for electronic device parts that are easy to handle and are averse to dust and static electricity. For this reason,
In-mold foam moldings made of pre-expanded polyolefin resin particles having antistatic properties have begun to be developed.

【0003】帯電防止性を付与する一般的な方法として
は、成形品表面に親水性界面活性剤を塗布する方法や、
あらかじめ樹脂に界面活性剤を練り込んだものから成形
品を製造する方法が代表的である。
As a general method for imparting antistatic property, a method of applying a hydrophilic surfactant on the surface of a molded article,
A typical method is to produce a molded product from a resin in which a surfactant is kneaded in advance.

【0004】前記あらかじめ樹脂に界面活性剤を練り込
んだものから成形品を製造する際に使用する帯電防止性
を付与したポリオレフィン系樹脂予備発泡粒子の例とし
て、ポリオレフィン系樹脂にHLB4〜8のノニオン系
界面活性剤を含有させた組成物からの粒子に発泡剤を含
浸させ、高温高圧下に保持したのちに低圧下に放出し、
ポリオレフィン系樹脂予備発泡粒子にしたものが提案さ
れている(特開平3−28239号公報)。
As an example of the pre-expanded polyolefin resin particles having an antistatic property, which is used in the production of a molded product from the above-described resin in which a surfactant is kneaded, nonionic nonionic resins of HLB 4 to 8 are used. Particles from a composition containing a system surfactant are impregnated with a foaming agent, held under high temperature and high pressure, and then released under low pressure,
It has been proposed to use polyolefin resin pre-expanded particles (Japanese Patent Laid-Open No. 3-28239).

【0005】なお、前記のノニオン系界面活性剤の例と
して、N,N−ジ(2−ヒドロキシエチル)アルキルア
ミン(以下、アルキルジエタノールアミンという)、脂
肪酸モノグリセライド、ソルビタン脂肪酸エステル、ア
ルキルジエタノールアミドが好適であると記載されてい
る。
As examples of the above nonionic surfactant, N, N-di (2-hydroxyethyl) alkylamine (hereinafter referred to as alkyldiethanolamine), fatty acid monoglyceride, sorbitan fatty acid ester, and alkyldiethanolamide are suitable. It is stated that there is.

【0006】[0006]

【発明が解決しようとする課題】しかしながら、前記の
ごとき帯電防止剤を用いれば、必ず良好な帯電防止性を
有する成形品がえられるというわけではなく、使用する
帯電防止剤によって帯電防止性に差があるのが実状であ
る。ポリオレフィン系樹脂型内発泡成形品の帯電防止性
が最もよくなるのは、帯電防止剤としてアルキルジエタ
ノールアミンを使用するばあいである。しかし、一般
に、フェノール系酸化防止剤を含むポリオレフィン系樹
脂の帯電防止剤としてアルキルジエタノールアミンを使
用したばあい、えられる成形品の養生・乾燥時や長期間
の保管中に黄変しやすく、とくに型内発泡成形品のばあ
い、蒸気を導入するスリット部分が黄味に変色し、まだ
ら模様となる。また、米国では、静電気防止の処理をし
たものには赤色系の色をつけることが規格(MIL−B
−81705)にあるため、有機顔料などを含有させて
樹脂粒子を着色させたばあい、成形品表面に色むらが生
じ、商品価値を著しく低下させやすいといった問題があ
る。また、前記色むらの問題を解決するためにポリオレ
フィン系樹脂に対する有機顔料の濃度を高めると、予備
発泡粒子の平均気泡径が微細化し、成形品の表面性が悪
化するという問題が生じる。
However, when the above-mentioned antistatic agent is used, a molded article having good antistatic property is not always obtained, and the antistatic property varies depending on the antistatic agent used. It is the actual situation that there is. The antistatic property of the foamed product in the polyolefin resin mold is best when the alkyldiethanolamine is used as the antistatic agent. However, in general, when alkyldiethanolamine is used as an antistatic agent for polyolefin resins containing phenolic antioxidants, the resulting molded articles tend to turn yellow during curing / drying or during long-term storage. In the case of an inner foamed product, the slits that introduce steam turn yellow and have a mottled pattern. In the United States, it is a standard (MIL-B
-81705), there is a problem that when the resin particles are colored by containing an organic pigment or the like, color unevenness occurs on the surface of the molded product, and the commercial value is apt to be significantly reduced. In addition, if the concentration of the organic pigment in the polyolefin resin is increased to solve the problem of color unevenness, the average bubble diameter of the pre-expanded particles becomes finer, which causes a problem that the surface property of the molded product deteriorates.

【0007】[0007]

【課題を解決するための手段】本発明者らは、かかる実
状に鑑み、黄変しにくく、良好な帯電防止性を有する、
優れたポリオレフィン系樹脂型内発泡成形品をうるべく
鋭意検討を重ねた結果、ポリオレフィン系樹脂に特定の
帯電防止剤を配合することにより前記問題を解決しうる
ことを見出した。さらに、一般的に使用しうる有機顔料
や染料などを含有して着色させるばあいにおいても特定
量の有機顔料を配合することにより表面性が良好で黄変
による色むらが生じないことを見出し、本発明を完成す
るに至った。
SUMMARY OF THE INVENTION In view of such circumstances, the present inventors have a tendency to prevent yellowing and have good antistatic properties.
As a result of intensive studies to obtain an excellent polyolefin-based resin in-mold molded article, it was found that the above-mentioned problems can be solved by blending a specific antistatic agent with the polyolefin-based resin. Furthermore, it has been found that even when containing an organic pigment or dye that can be generally used for coloring, by mixing a specific amount of the organic pigment, the surface property is good and color unevenness due to yellowing does not occur, The present invention has been completed.

【0008】すなわち、本発明は、ポリオレフィン系樹
脂100部(重量部、以下同様)に対し、一般式
(1):
That is, the present invention is based on the general formula (1):

【0009】[0009]

【化3】 Embedded image

【0010】(式中、Rは炭素数8〜22のアルキル
基)で示されるヒドロキシアルキルモノエタノールアミ
ンを0.05〜5部含有するポリオレフィン系樹脂組成
物の粒子から形成された帯電防止性を有するポリオレフ
ィン系樹脂予備発泡粒子、ポリオレフィン系樹脂100
部に対し、前記一般式(1)で示されるヒドロキシアル
キルモノエタノールアミン0.05〜5部に加えて、さ
らに有機顔料を0.005〜0.1部含有するポリオレ
フィン系樹脂組成物の粒子から形成された帯電防止性を
有するポリオレフィン系樹脂予備発泡粒子、ポリオレフ
ィン系樹脂100部に対し、一般式(1):
(Wherein R is an alkyl group having 8 to 22 carbon atoms), an antistatic property formed from particles of a polyolefin resin composition containing 0.05 to 5 parts of a hydroxyalkyl monoethanolamine is shown. Pre-expanded polyolefin resin particles, polyolefin resin 100
In addition to 0.05 to 5 parts of the hydroxyalkyl monoethanolamine represented by the general formula (1), 0.005 to 0.1 part of an organic pigment is further added to the polyolefin resin composition particles. Based on 100 parts of the formed polyolefin resin pre-expanded particles having antistatic properties and the polyolefin resin, the general formula (1):

【0011】[0011]

【化4】 [Chemical 4]

【0012】(式中、Rは炭素数8〜22のアルキル
基)で示されるヒドロキシアルキルモノエタノールアミ
ンを0.05〜5部含有するポリオレフィン系樹脂組成
物の粒子を、耐圧容器内に、水、分散剤および揮発性発
泡剤とともに仕込み、水分散物となし、該粒子の融点−
20℃から+20℃の範囲の温度で、該樹脂粒子に揮発
性発泡剤を含浸させ、加圧下、前記水分散物を容器内よ
りも低圧の雰囲気下に放出することを特徴とする帯電防
止性を有するポリオレフィン系樹脂予備発泡粒子の製法
およびポリオレフィン系樹脂100部に対し、前記一般
式(1)で示されるヒドロキシアルキルモノエタノール
アミン0.05〜5部に加えて、さらに有機顔料を0.
005〜0.1部含有するポリオレフィン系樹脂組成物
からの粒子を使用する前記帯電防止性を有するポリオレ
フィン系樹脂予備発泡粒子の製法に関する。
Particles of a polyolefin resin composition containing 0.05 to 5 parts of a hydroxyalkyl monoethanolamine represented by the formula (wherein R is an alkyl group having 8 to 22 carbon atoms) are treated with water in a pressure resistant container. , A dispersant and a volatile foaming agent to prepare an aqueous dispersion, and the melting point of the particles-
Antistatic property, characterized in that the resin particles are impregnated with a volatile foaming agent at a temperature in the range of 20 ° C. to + 20 ° C., and the aqueous dispersion is released under pressure to a lower pressure atmosphere than in the container. In addition to 0.05 to 5 parts of the hydroxyalkyl monoethanolamine represented by the above general formula (1), an organic pigment of 0.1 part is added to 100 parts of the polyolefin resin pre-expanded particles having the above formula.
The present invention relates to a method for producing pre-expanded polyolefin resin particles having antistatic properties, which comprises using particles from a polyolefin resin composition containing 005 to 0.1 part.

【0013】[0013]

【実施例】本発明でいうポリオレフィン系樹脂とは、オ
レフィン単位を50%以上含み、好ましくはMIが0.
1〜50g/10分の樹脂のことである。
EXAMPLES The polyolefin resin referred to in the present invention contains 50% or more of olefin units and preferably has an MI of 0.1.
It is a resin of 1 to 50 g / 10 minutes.

【0014】前記ポリオレフィン系樹脂の具体例として
は、たとえば高密度ポリエチレン(HDPE)、中密度
ポリエチレン(MDPE)、低密度ポリエチレン(LD
PE)、直鎖状低密度ポリエチレン(LLDPE)、低
分子量ポリエチレンなどのポリエチレン類、ポリプロピ
レン、低分子量ポリプロピレンなどのポリプロピレン
類、ポリブテンなどのその他のポリオレフィンホモポリ
マー類、エチレン−プロピレンランダム共重合体、エチ
レン−プロピレンブロック共重合体、エチレン−酢酸ビ
ニル共重合体(EVA)、エチレン−塩化ビニル共重合
体、エチレン−酢酸ビニル−ビニルアルコール共重合体
などのエチレン系共重合体類、プロピレン−1−ブテン
共重合体、プロピレン−エチレン−ブテンランダムター
ポリマーなどのプロピレン系共重合体類などや、これら
を必要により架橋させたものなどがあげられるが、これ
らに限定されるものではない。これらのうちでは、直鎖
状低密度ポリエチレン(LLDPE)、エチレン−プロ
ピレンランダム共重合体、エチレン−プロピレン−ブテ
ン3元共重合体がビーズ発泡性、型内成形性が優れる点
で好ましい。
Specific examples of the polyolefin resin include high density polyethylene (HDPE), medium density polyethylene (MDPE) and low density polyethylene (LD).
PE), linear low density polyethylene (LLDPE), polyethylene such as low molecular weight polyethylene, polypropylene, polypropylene such as low molecular weight polypropylene, other polyolefin homopolymers such as polybutene, ethylene-propylene random copolymer, ethylene -Ethylene-based copolymers such as propylene block copolymer, ethylene-vinyl acetate copolymer (EVA), ethylene-vinyl chloride copolymer, ethylene-vinyl acetate-vinyl alcohol copolymer, propylene-1-butene Examples thereof include, but are not limited to, copolymers, propylene-based copolymers such as propylene-ethylene-butene random terpolymer, and those obtained by crosslinking these as necessary. Of these, linear low-density polyethylene (LLDPE), ethylene-propylene random copolymer, and ethylene-propylene-butene terpolymer are preferable in terms of bead foamability and in-mold moldability.

【0015】これらは単独で用いてもよく、2種以上併
用してもよい。
These may be used alone or in combination of two or more.

【0016】本発明においては、前記ポリオレフィン系
樹脂に、帯電防止剤である一般式(1):
In the present invention, the above-mentioned polyolefin-based resin has the general formula (1) as an antistatic agent:

【0017】[0017]

【化5】 Embedded image

【0018】(式中、Rは炭素数8〜22のアルキル
基)で表わされるヒドロキシアルキルモノエタノールア
ミンが加えられる。
A hydroxyalkyl monoethanolamine represented by the formula (wherein R is an alkyl group having 8 to 22 carbon atoms) is added.

【0019】一般式(1)で表わされるヒドロキシアル
キルモノエタノールアミンはえられる型内発泡成形品の
帯電防止性を良好にし、かつ成形性、成形品の耐変色性
などを良好に維持する。
The hydroxyalkyl monoethanolamine represented by the general formula (1) improves the antistatic property of the obtained in-mold foamed molded product, and also maintains the moldability and discoloration resistance of the molded product.

【0020】前記一般式(1)中のRの炭素数は8〜2
2であるが、8未満のばあい、あるいは22をこえるば
あい、帯電防止効果は不充分となり、好ましくない。
The carbon number of R in the general formula (1) is 8 to 2.
If it is 2, but less than 8 or more than 22, the antistatic effect becomes insufficient, which is not preferable.

【0021】前記一般式(1)中のRの具体例として
は、たとえばオクチル基、ノニル基、ペンタデシル基、
ヘキサデシル基、ヘプタデシル基、オクタデシル基のご
とき直鎖のアルキル基などが好ましい例としてあげられ
るが、これらに限定されるものではない。
Specific examples of R in the general formula (1) include, for example, an octyl group, a nonyl group, a pentadecyl group,
Preferred examples include linear alkyl groups such as a hexadecyl group, a heptadecyl group, and an octadecyl group, but the present invention is not limited thereto.

【0022】本発明におけるポリオレフィン系樹脂10
0部に対する一般式(1)で表わされるヒドロキシアル
キルモノエタノールアミン(帯電防止剤)の添加量は
0.05〜5部、好ましくは0.1〜3部である。前記
帯電防止剤の添加量が0.05部未満のばあい、充分な
帯電防止効果をうることができず、一方、5部をこえる
と、えられる成形品の表面にべとつきが生じやすくな
る。
Polyolefin resin 10 in the present invention
The addition amount of the hydroxyalkyl monoethanolamine (antistatic agent) represented by the general formula (1) to 0 part is 0.05 to 5 parts, preferably 0.1 to 3 parts. When the amount of the antistatic agent added is less than 0.05 part, a sufficient antistatic effect cannot be obtained, while when it exceeds 5 parts, the resulting molded article tends to be sticky.

【0023】前記帯電防止剤は、他の帯電防止剤(たと
えばグリセリン脂肪酸エステル、アルキルジエタノール
アミド、ソルビタン脂肪酸エステルなどのノニオン界面
活性剤やカチオン界面活性剤あるいは両性界面活性剤な
どの帯電防止剤)と併用して使用しても差し支えない。
The antistatic agent is combined with another antistatic agent (for example, a nonionic surfactant such as glycerin fatty acid ester, alkyldiethanolamide, sorbitan fatty acid ester or the like, a cationic surfactant or an antistatic agent such as an amphoteric surfactant). It can be used together.

【0024】併用するばあい、一般式(1)で表わされ
るヒドロキシアルキルモノエタノールアミンを50%以
上含有させることが、帯電防止性、耐変色性などの点か
ら好ましい。
When used in combination, it is preferable that the hydroxyalkyl monoethanolamine represented by the general formula (1) is contained in an amount of 50% or more from the viewpoints of antistatic property and discoloration resistance.

【0025】ポリオレフィン系樹脂と帯電防止剤との混
合順序、混合の仕方などにはとくに限定はないが、ポリ
オレフィン系樹脂の一部と一般式(1)で表わされるヒ
ドロキシアルキルモノエタノールアミンとから、まず、
帯電防止剤含有率の高いマスターバッチ、たとえば帯電
防止剤の含有率が5〜20%のマスターバッチを調製
し、これとのこりのポリオレフィン系樹脂とを混合する
方法が帯電防止剤を均一に分散させやすいという点から
好ましい。
The order of mixing the polyolefin resin and the antistatic agent, the manner of mixing, etc. are not particularly limited, but from a part of the polyolefin resin and the hydroxyalkyl monoethanolamine represented by the general formula (1), First,
A method of preparing a masterbatch having a high content rate of the antistatic agent, for example, a masterbatch having a content rate of the antistatic agent of 5 to 20% and mixing the masterbatch with the residual polyolefin resin is to uniformly disperse the antistatic agent. It is preferable because it is easy.

【0026】本発明に用いる前記ポリオレフィン系樹脂
と一般式(1)で表わされるヒドロキシアルキルモノエ
タノールアミンとからなるポリオレフィン系樹脂組成物
には、有機顔料を加えてもよい。
An organic pigment may be added to the polyolefin resin composition comprising the polyolefin resin used in the present invention and the hydroxyalkyl monoethanolamine represented by the general formula (1).

【0027】前記有機顔料としては、たとえばペリレン
系、ポリアゾ系の有機顔料が使用されるが、これらに限
定されるものではない。
As the organic pigment, for example, a perylene-based or polyazo-based organic pigment is used, but the organic pigment is not limited thereto.

【0028】前記有機顔料の含有量はポリオレフィン系
樹脂100部に対し、0.005〜0.1部の範囲が分
散性や帯電防止性の点から好ましい。前記含有量が0.
1部をこえると予備発泡粒子の気泡径が微細となり、成
形品の表面性が劣り、見栄えがわるくなる傾向にある。
The content of the organic pigment is preferably 0.005 to 0.1 part with respect to 100 parts of the polyolefin resin from the viewpoint of dispersibility and antistatic property. The content is 0.
If it exceeds 1 part, the bubble diameter of the pre-expanded particles tends to be fine, and the surface properties of the molded product tend to be poor, resulting in a poor appearance.

【0029】ポリオレフィン系樹脂と有機顔料との混合
順序、混合の仕方などにはとくに限定はないが、前記ポ
リオレフィン系樹脂と帯電防止剤のばあいと同様、まず
顔料含有率の高いマスターバッチ、たとえば顔料含有率
が0.1〜5%のマスターバッチを調製し、これにのこ
りのポリオレフィン系樹脂を混合する方法が顔料を均一
に分散させやすいという点から好ましい。
The order of mixing the polyolefin resin and the organic pigment and the manner of mixing are not particularly limited, but as in the case of the polyolefin resin and the antistatic agent, first, a masterbatch having a high pigment content, for example, It is preferable to prepare a masterbatch having a pigment content of 0.1 to 5% and mix it with a residual polyolefin resin because the pigment can be easily dispersed uniformly.

【0030】本発明のポリオレフィン系樹脂予備発泡粒
子は、前記のごときポリオレフィン系樹脂と帯電防止剤
とからなる組成物からの粒子を予備発泡させた帯電防止
性を有する予備発泡粒子、さらには、前記組成物に特定
量の有機顔料を加えた粒子を予備発泡させた帯電防止性
を有する予備発泡粒子である。
The pre-expanded polyolefin resin particles of the present invention are pre-expanded particles having antistatic properties obtained by pre-expanding particles from the composition comprising the polyolefin resin and the antistatic agent as described above, and further The pre-expanded particles having antistatic properties are obtained by pre-expanding particles obtained by adding a specific amount of an organic pigment to the composition.

【0031】前記粒子の大きさは一般に0.5〜10m
g/粒程度のものであり、本発明の予備発泡粒子はこの
ような粒子を、通常5〜60倍程度、好ましくは10〜
40程度に予備発泡させたものである。
The size of the particles is generally 0.5 to 10 m.
g / grain, and the pre-expanded particles of the present invention contain such particles in an amount of usually 5 to 60 times, preferably 10 to
It is pre-foamed to about 40.

【0032】前記予備発泡粒子の密度は、要すれば使用
される充填剤の有無、樹脂密度などによっても異なる
が、通常0.18〜0.015g/cc、さらには0.
09〜0.022g/cc程度のものである。
The density of the pre-expanded particles is usually 0.18 to 0.015 g / cc, more preferably 0.
It is about 09 to 0.022 g / cc.

【0033】なお、前記粒子やマスターバッチは、ポリ
オレフィン系樹脂と帯電防止剤、有機顔料(マスターバ
ッチとして加えられるばあいを含む)などとを押出機内
で溶融混練したのち、複数個の開口部を通してストラン
ド状に押し出し、空中または水中で冷却後、ストランド
をカットして造粒することにより製造される。マスター
バッチを使用するばあいには、帯電防止剤、有機顔料な
どのかわりにマスターバッチを使用すればよい。
The particles and the masterbatch are prepared by melt-kneading a polyolefin resin, an antistatic agent, an organic pigment (including the case where it is added as a masterbatch) in an extruder, and then through a plurality of openings. It is produced by extruding into a strand shape, cooling in air or water, and then cutting and granulating the strand. When using a masterbatch, the masterbatch may be used instead of the antistatic agent, the organic pigment and the like.

【0034】つぎに本発明のポリオレフィン系樹脂予備
発泡粒子の製法について説明する。
Next, a method of producing the polyolefin resin pre-expanded particles of the present invention will be described.

【0035】前述のごとき帯電防止剤および有機顔料な
どを含有するポリオレフィン系樹脂組成物からの粒子と
揮発性発泡剤を分散剤の存在下で水に分散させ、該粒子
の融点より−20℃から+20℃の範囲の温度に加熱し
て該粒子内に揮発性発泡剤を含浸させ、加圧下、前記水
分散物を容器内よりも低圧の雰囲気下に放出することに
より、本発明の予備発泡粒子が製造される。水分散物を
容器内より低圧の雰囲気下に放出する際に容器内の温
度、圧力を一定に保持しながら放出することにより、発
泡倍率のバラツキが小さい予備発泡粒子がえられる。
Particles of a polyolefin resin composition containing an antistatic agent and an organic pigment as described above and a volatile foaming agent are dispersed in water in the presence of a dispersant, and the melting point of the particles is from -20 ° C. Pre-expanded particles of the present invention by heating to a temperature in the range of + 20 ° C. to impregnate the particles with a volatile foaming agent and releasing the aqueous dispersion under pressure under an atmosphere at a pressure lower than that in the container. Is manufactured. When the water dispersion is discharged under a lower pressure atmosphere than the inside of the container, the temperature and pressure inside the container are kept constant, whereby pre-expanded particles having a small variation in expansion ratio can be obtained.

【0036】前記揮発性発泡剤としては、沸点が−50
〜+120℃の炭化水素類またはハロゲン化炭化水素類
など、たとえばプロパン、ブタン、ペンタン、ヘキサ
ン、ヘプタン、シクロヘキサンなどの炭化水素類、モノ
クロロメタン、ジクロロメタン、モノクロロエタン、ト
リクロロモノフルオロメタン、ジクロロジフルオロエタ
ン、ジクロロジフルオロメタン、ジクロロモノフルオロ
エタン、トリクロロトリフルオロエタン、ジクロロテト
ラフルオロエタンなどのハロゲン化炭化水素類などが使
用される。これらは単独で用いてもよく2種以上併用し
てもよい。
The volatile foaming agent has a boiling point of -50.
Hydrocarbons or halogenated hydrocarbons at up to + 120 ° C., for example, hydrocarbons such as propane, butane, pentane, hexane, heptane, cyclohexane, monochloromethane, dichloromethane, monochloroethane, trichloromonofluoromethane, dichlorodifluoroethane, dichloro Halogenated hydrocarbons such as difluoromethane, dichloromonofluoroethane, trichlorotrifluoroethane and dichlorotetrafluoroethane are used. These may be used alone or in combination of two or more.

【0037】これらの揮発性発泡剤の使用量は、発泡剤
の種類、所望する発泡倍率、容器内の粒子量と容器内空
間容積との比率を考慮して、該粒子中の樹脂に対して5
〜40%含浸されるようにするのが好ましい。
The amount of these volatile foaming agents used is determined with respect to the resin in the particles in consideration of the type of the foaming agent, the desired expansion ratio, the ratio of the amount of particles in the container to the space volume in the container. 5
Preferably ~ 40% impregnation.

【0038】前記分散剤としては、分散剤として一般に
使用されている、たとえば第3リン酸カルシウム、ピロ
リン酸マグネシウム、炭酸亜鉛などの水に難溶性の無機
物質が使用される。また、少量のドデシルベンゼンスル
フォン酸ナトリウム、α−オレフィンスルフォン酸ナト
リウムなどの一般に分散助剤として使用されているアニ
オン界面活性剤を分散助剤として併用しうる。
As the dispersant, an inorganic substance which is generally used as a dispersant, such as tricalcium phosphate, magnesium pyrophosphate, zinc carbonate or the like, which is poorly soluble in water, is used. Further, a small amount of anionic surfactant, which is generally used as a dispersion aid, such as sodium dodecylbenzene sulfonate or sodium α-olefin sulfonate may be used together as a dispersion aid.

【0039】また、分散剤の使用量についても一般に使
用される量であり、ポリオレフィン系樹脂100部に対
して0.1〜5部程度である。また、分散助剤を使用す
るばあいの使用量も、ポリオレフィン系樹脂100部に
対して0.001〜0.3部程度という一般的な量であ
るが、とくにこの範囲に制限されるものではない。
The amount of the dispersant used is also a commonly used amount, and is about 0.1 to 5 parts with respect to 100 parts of the polyolefin resin. The amount of the dispersion aid used is generally 0.001 to 0.3 parts per 100 parts of the polyolefin resin, but is not particularly limited to this range. .

【0040】さらに、水分散物中における予備発泡前の
粒子の割合も一般に採用される割合である水100部に
対して20〜100部であるかぎり、とくに制限はな
い。
Further, the ratio of particles before pre-foaming in the water dispersion is not particularly limited as long as it is 20 to 100 parts with respect to 100 parts of water which is a generally adopted ratio.

【0041】前記粒子の融点より−20℃から+20℃
の範囲の温度は、セイコー電子工業(株)製のDSC2
20を用い、昇温速度が10℃/分の条件で測定した融
点を基準にした温度である。融点より−20℃から+2
0℃、好ましくは−10℃から+10℃の範囲の温度に
加熱して揮発性発泡剤が含浸せしめられる。
From the melting point of the particles, -20 ° C to + 20 ° C
The temperature range is DSC2 manufactured by Seiko Instruments Inc.
20 is the temperature based on the melting point measured under the condition that the temperature rising rate is 10 ° C./min. -20 to +2 from melting point
The volatile blowing agent is impregnated by heating to a temperature in the range 0 ° C, preferably -10 ° C to + 10 ° C.

【0042】前記温度が(融点−20℃)よりも低いば
あいには、目的とする倍率の予備発泡粒子がえられにく
くなり、また(融点+20℃)よりも高いばあいには、
樹脂の溶融粘度が低下しすぎて予備発泡粒子の独立気泡
率が低下する。
When the temperature is lower than (melting point -20 ° C), it becomes difficult to obtain the pre-expanded particles having a target magnification, and when the temperature is higher than (melting point + 20 ° C),
The melt viscosity of the resin is lowered too much, and the closed cell ratio of the pre-expanded particles is lowered.

【0043】また、前記容器内よりも低圧の雰囲気下と
は、一般に予備発泡粒子を製造する際に、容器中の水分
散物を放出する低圧の雰囲気として採用される条件であ
るかぎりとくに制限はないが、たとえば大気中に放出す
る際には大気下、揮発性発泡剤を回収するために密閉系
内に放出するばあいには密閉系内の雰囲気下のことであ
る。
The atmosphere under a pressure lower than that in the container is not particularly limited as long as it is a condition under which a low-pressure atmosphere for releasing the water dispersion in the container is generally used when producing the pre-expanded particles. For example, when it is released into the air, it is under the atmosphere, and when it is released into the closed system to recover the volatile foaming agent, it is under the atmosphere of the closed system.

【0044】以上のようにして、本発明の予備発泡粒子
が製造される。
The pre-expanded particles of the present invention are manufactured as described above.

【0045】また、えられた予備発泡粒子は、成形性、
融着性が良好で、通常の型内発泡成形により良好な成形
品にすることができるものである。
Further, the obtained pre-expanded particles have moldability,
The meltability is good, and a good molded product can be obtained by ordinary in-mold foam molding.

【0046】以上のようにしてえられた予備発泡粒子
は、発泡粒子中の発泡剤を空気と置換したのち、必要に
応じて内圧付与をするかもしくはそのまま内圧付与をし
ないで成形型内に充填し、0.7〜4.0kg/cm2
(G)程度の水蒸気で粒子同士を融着させ、金型から取
り出したのち、60℃から80℃の乾燥室で24時間程
度養生させることにより成形品がえられる。
The pre-expanded particles obtained as described above are filled in a molding die after the blowing agent in the expanded particles is replaced with air, and then internal pressure is applied as necessary or without applying internal pressure as it is. 0.7-4.0 kg / cm 2
The particles are fused with water vapor of about (G), taken out from the mold, and then aged in a drying chamber at 60 ° C. to 80 ° C. for about 24 hours to obtain a molded product.

【0047】さらに、えられた成形品は各種用途に使用
されるが、特定の帯電防止剤を使用しているため、該成
形品の耐変色性および帯電防止性は高い水準で良好であ
る。
Further, the obtained molded product is used for various purposes, but since a specific antistatic agent is used, the discoloration resistance and antistatic property of the molded product are excellent at a high level.

【0048】以下、本発明を実施例に基づきさらに詳細
に説明する。
Hereinafter, the present invention will be described in more detail based on examples.

【0049】実施例1〜3および比較例1〜4 フェノール系酸化防止剤(オクタデシル−3−(3,5
−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオ
ネート)0.15部を含有した密度0.93g/c
3 、MI2.0g/10分の直鎖状低密度ポリエチレ
ン(DSC融点124℃)100部と、表1に示す種
類、量の帯電防止剤と有機顔料とを混合し、50mmφ
の押出機で混練(210℃)したのち造粒し、予備発泡
前の粒子(4.5mg/粒)を製造した。
Examples 1 to 3 and Comparative Examples 1 to 4 Phenolic antioxidant (octadecyl-3- (3,5
-Di-t-butyl-4-hydroxyphenyl) propionate) containing 0.15 parts density 0.93 g / c
m 3, were mixed with MI2.0g / 10 min linear low density polyethylene (DSC melting point 124 ° C.) 100 parts, the type shown in Table 1, the antistatic agent and the organic pigment in an amount, 50 mm [phi]
After kneading (210 ° C.) with an extruder of No. 1 and granulating, particles (4.5 mg / grain) before pre-expansion were produced.

【0050】10リットル耐圧容器に、水300部、え
られた粒子100部、分散剤および分散助剤として第3
リン酸カルシウム2.0部とノルマルパラフィンスルフ
ォン酸ソーダ0.03部とを仕込み、さらにイソブタン
を15部仕込み、撹拌下、表1に示す温度および内圧で
30分間保持したのち、容器内をチッ素ガスで前記内圧
に保持しながら容器の下部に設けた5mmφオリフィス
を通して水分散物を大気圧下に放出し、予備発泡粒子を
えた。そののち水で洗浄し、乾燥させた。
In a 10-liter pressure vessel, 300 parts of water, 100 parts of the obtained particles, a third dispersant and a third dispersion aid were used.
2.0 parts of calcium phosphate and 0.03 part of normal paraffin sodium sulfonate were charged, 15 parts of isobutane was further charged, and the contents were kept for 30 minutes at the temperature and internal pressure shown in Table 1 under stirring. Then, the inside of the container was filled with nitrogen gas. While maintaining the internal pressure, the aqueous dispersion was discharged under atmospheric pressure through a 5 mmφ orifice provided in the lower part of the container to obtain pre-expanded particles. After that, it was washed with water and dried.

【0051】えられた予備発泡粒子の発泡倍率をThe expansion ratio of the obtained pre-expanded particles

【0052】[0052]

【数1】 [Equation 1]

【0053】より求めた。結果を表1に示す。Calculated from Table 1 shows the results.

【0054】つぎに、えられた予備発泡粒子を450m
m×300mm×50mmの金型に充填し、予備発泡粒
子同士を0.8kg/cm2 (G)の水蒸気にて加熱、
融着させ、型内成形品をえ、金型から取り出した。金型
から取り出した成形品を80℃の乾燥器中で24時間乾
燥、養生したのち、成形品の物性(成形品の発泡倍率、
表面性、融着性、耐変色性、表面固有抵抗)を下記方法
により評価した。結果を表1に示す。
Next, 450 m of the obtained pre-expanded particles are added.
It is filled in a mold of m × 300 mm × 50 mm, and the pre-expanded particles are heated with 0.8 kg / cm 2 (G) of steam,
After fusion, an in-mold molded product was obtained and taken out from the mold. After the molded product taken out of the mold is dried and cured in an oven at 80 ° C for 24 hours, the physical properties of the molded product (foaming ratio of molded product,
The surface properties, fusion properties, discoloration resistance, and surface resistivity) were evaluated by the following methods. The results are shown in Table 1.

【0055】(成形品の発泡倍率)成形品の重量と成形
品の体積を求め
(Expansion Ratio of Molded Product) The weight of the molded product and the volume of the molded product are obtained.

【0056】[0056]

【数2】 [Equation 2]

【0057】より求めた。Obtained from

【0058】(表面性)成形品表面を目視で観察し、下
記基準にしたがって評価した。
(Surface property) The surface of the molded product was visually observed and evaluated according to the following criteria.

【0059】○:表面粒子間の凹凸が少なく、表面が平
滑である △:表面粒子間の凹凸がやや多く、表面平滑性にやや欠
ける ×:表面粒子間の凹凸が多く、表面平滑性に欠ける (融着性)成形品を破断させて断面を観察し、下記基準
にしたがって評価した。
◯: There are few irregularities between the surface particles and the surface is smooth. Δ: There are a large number of irregularities between the surface particles and the surface smoothness is slightly poor. X: There are many irregularities between the surface particles and the surface smoothness is poor. (Fusability) The molded product was broken and the cross section was observed and evaluated according to the following criteria.

【0060】○:粒子が破断している割合が60%以上 ×:粒子が破断している割合が60%未満 (耐変色性)成形体表面の着色状態を目視観察し、下記
基準にしたがって評価した。
◯: Particle breakage ratio is 60% or more ×: Particle breakage ratio is less than 60% (Discoloration resistance) The colored state of the surface of the molded product is visually observed and evaluated according to the following criteria. did.

【0061】○ :黄変が認められない × :黄変が著しい (表面固有抵抗)成形品を温度23℃、湿度50%の室
内に48時間保存し、状態を調節したのち、アドバンテ
スト(株)製の超絶縁抵抗計TR8601を用いて測定
し、下記基準にしたがって評価した。
◯: No yellowing was observed ×: Significant yellowing (surface resistivity) The molded product was stored in a room at a temperature of 23 ° C. and a humidity of 50% for 48 hours, and after adjusting the condition, Advantest Co., Ltd. It was measured using a super insulation resistance meter TR8601 manufactured by and manufactured according to the following criteria.

【0062】○:1×1011Ω未満 △:1×1011Ω以上〜1×1012Ω未満 ×:1×1012Ω以上[0062] ○: 1 × 10 of less than 11 Ω △: 1 × 10 11 Ω or more ~1 × 10 of less than 12 Ω ×: 1 × 10 12 Ω or more

【0063】[0063]

【表1】 [Table 1]

【0064】実施例4〜6および比較例5〜8 フェノール系酸化防止剤(BHT)0.2部を含有する
エチレン含有率3.2%のエチレン−プロピレンランダ
ム共重合体(DSC融点145℃)100部と、表2に
示す種類、量の帯電防止剤と有機顔料とを混合し、50
mmφの押出機で混練(220℃)したのち、造粒し、
予備発泡前の粒子(1.8mg/粒)を製造した。
Examples 4 to 6 and Comparative Examples 5 to 8 Ethylene-propylene random copolymer (DSC melting point 145 ° C.) containing 0.2 part of phenolic antioxidant (BHT) and having an ethylene content of 3.2%. 50 parts of the antistatic agent and organic pigment of the type and amount shown in Table 2 are mixed,
After kneading (220 ° C) with an mmφ extruder, granulate,
Particles (1.8 mg / grain) before pre-expansion were produced.

【0065】10リットル耐圧容器に、水300部、え
られた粒子100部、分散剤および分散助剤として第3
リン酸カルシウム2.0部とノルマンパラフィンスルフ
ォン酸ソーダ0.03部とを仕込み、さらに、イソブタ
ンを11部仕込み、撹拌下、表2に示す温度および内圧
で30分間保持したのち、容器内をチッ素ガスで前記内
圧に保持しながら容器の下部に設けた5mmφオリフィ
スを通して水分散物を大気圧下に放出し、予備発泡粒子
をえた。そののち水で洗浄し、乾燥させた。
In a 10 liter pressure vessel, 300 parts of water, 100 parts of the obtained particles, a third as a dispersant and a dispersion aid.
After charging 2.0 parts of calcium phosphate and 0.03 part of sodium norman paraffin sulfonate, 11 parts of isobutane were further charged, and the contents were kept for 30 minutes at the temperature and internal pressure shown in Table 2 under stirring. While maintaining the internal pressure, the water dispersion was discharged under atmospheric pressure through a 5 mmφ orifice provided at the bottom of the container to obtain pre-expanded particles. After that, it was washed with water and dried.

【0066】えられた予備発泡粒子の発泡倍率を実施例
1と同様にして求めた。結果を表2に示す。
The expansion ratio of the obtained pre-expanded particles was determined in the same manner as in Example 1. Table 2 shows the results.

【0067】つぎに、えられた予備発泡粒子を200リ
ットル耐圧容器に仕込み、8kg/cm2 (G)に加圧
し、2時間保持して予備発泡粒子の内圧を1kg/cm
2 (G)に高めたのち450mm×300mm×50m
mの金型に充填し、発泡粒子同士を3kg/cm
2 (G)の水蒸気にて加熱、融着させ、型内成形品を
え、金型から取り出した。金型から取り出した成形品を
70℃の乾燥器中で24時間乾燥、養生したのち、成形
品の物性を実施例1と同様にして測定した。結果を表2
に示す。
Next, the obtained pre-expanded particles were charged into a 200 liter pressure resistant container, pressurized to 8 kg / cm 2 (G), and held for 2 hours to set the internal pressure of the pre-expanded particles to 1 kg / cm.
450 mm x 300 mm x 50 m after raising to 2 (G)
3 m / cm of the expanded particles filled in the m mold
2 (G) was heated and fused with water vapor to obtain an in-mold molded product, which was taken out of the mold. The molded product taken out from the mold was dried and cured in a dryer at 70 ° C. for 24 hours, and the physical properties of the molded product were measured in the same manner as in Example 1. Table 2 shows the results
Shown in

【0068】[0068]

【表2】 [Table 2]

【0069】[0069]

【発明の効果】本発明の予備発泡粒子を用いて成形品を
製造すると、耐変色性および帯電防止性がいずれも良好
で、べたつきが少なく、粒子間の融着性の良好な成形品
を容易にうることができる。
EFFECTS OF THE INVENTION When a molded product is produced using the pre-expanded particles of the present invention, it is easy to obtain a molded product having good discoloration resistance and antistatic property, little stickiness, and good fusion between particles. You can get it.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 ポリオレフィン系樹脂100重量部に対
し、一般式(1): 【化1】 (式中、Rは炭素数8〜22のアルキル基)で示される
ヒドロキシアルキルモノエタノールアミンを0.05〜
5重量部含有するポリオレフィン系樹脂組成物の粒子か
ら形成された帯電防止性を有するポリオレフィン系樹脂
予備発泡粒子。
1. A compound represented by the general formula (1): embedded image with respect to 100 parts by weight of a polyolefin resin. (In the formula, R is an alkyl group having 8 to 22 carbon atoms), and a hydroxyalkyl monoethanolamine of 0.05 to
Pre-expanded polyolefin resin particles having antistatic properties, which are formed from 5 parts by weight of particles of the polyolefin resin composition.
【請求項2】 ポリオレフィン系樹脂100重量部に対
し、さらに有機顔料を0.005〜0.1重量部含有す
るポリオレフィン系樹脂組成物の粒子を使用した請求項
1記載のポリオレフィン系樹脂予備発泡粒子。
2. The polyolefin resin pre-expanded particles according to claim 1, wherein particles of the polyolefin resin composition further containing 0.005 to 0.1 part by weight of an organic pigment are used with respect to 100 parts by weight of the polyolefin resin. .
【請求項3】 ポリオレフィン系樹脂100重量部に対
し、一般式(1): 【化2】 (式中、Rは炭素数8〜22のアルキル基)で示される
ヒドロキシアルキルモノエタノールアミンを0.05〜
5重量部含有するポリオレフィン系樹脂組成物の粒子
を、耐圧容器内に、水、分散剤および揮発性発泡剤とと
もに仕込み、水分散物となし、該粒子の融点−20℃か
ら+20℃の範囲の温度で、該粒子に揮発性発泡剤を含
浸させ、加圧下、前記水分散物を容器内よりも低圧の雰
囲気下に放出することを特徴とする帯電防止性を有する
ポリオレフィン系樹脂予備発泡粒子の製法。
3. A compound represented by the general formula (1): embedded image with respect to 100 parts by weight of the polyolefin resin. (In the formula, R is an alkyl group having 8 to 22 carbon atoms), and a hydroxyalkyl monoethanolamine of 0.05 to
Particles of a polyolefin resin composition containing 5 parts by weight were charged into a pressure resistant container together with water, a dispersant and a volatile foaming agent to form an aqueous dispersion, and the melting point of the particles was from -20 ° C to + 20 ° C. A polyolefin resin pre-expanded particle having antistatic properties, characterized in that the particle is impregnated with a volatile foaming agent at a temperature, and the aqueous dispersion is released under pressure under an atmosphere at a pressure lower than that in a container. Manufacturing method.
【請求項4】 ポリオレフィン系樹脂100重量部に対
し、さらに有機顔料を0.005〜0.1重量部含有す
るポリオレフィン系樹脂組成物の粒子を使用する請求項
3記載の製法。
4. The method according to claim 3, wherein particles of a polyolefin resin composition further containing 0.005 to 0.1 parts by weight of an organic pigment are used with respect to 100 parts by weight of the polyolefin resin.
JP14617194A 1994-06-28 1994-06-28 Pre-expanded polyolefin resin particles having antistatic properties and method for producing the same Expired - Lifetime JP3456758B2 (en)

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JP14617194A JP3456758B2 (en) 1994-06-28 1994-06-28 Pre-expanded polyolefin resin particles having antistatic properties and method for producing the same

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Application Number Priority Date Filing Date Title
JP14617194A JP3456758B2 (en) 1994-06-28 1994-06-28 Pre-expanded polyolefin resin particles having antistatic properties and method for producing the same

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JPH0812798A true JPH0812798A (en) 1996-01-16
JP3456758B2 JP3456758B2 (en) 2003-10-14

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Cited By (6)

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JP2003082169A (en) * 2001-09-13 2003-03-19 Kao Corp Polyolefin resin composition
WO2009001645A1 (en) * 2007-06-22 2008-12-31 Kaneka Corporation Polyolefin resin pre-foamed particle having antistatic property, and molded article produced from the particle
JP2009215438A (en) * 2008-03-11 2009-09-24 Kaneka Corp Method for producing polypropylene-based resin pre-foamed particle
JP4781998B2 (en) * 2004-02-24 2011-09-28 株式会社カネカ Method for producing polyolefin pre-expanded particles using water as a foaming agent
WO2013137411A1 (en) 2012-03-14 2013-09-19 株式会社カネカ Polypropylene resin foam particles, in-mold foam molded body comprising polypropylene resin foam particles, and method for producing same
US9611369B2 (en) 2012-03-14 2017-04-04 Kaneka Corporation In-mold foam molded body comprising polypropylene resin foam particles and method for producing same

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003082169A (en) * 2001-09-13 2003-03-19 Kao Corp Polyolefin resin composition
JP4619586B2 (en) * 2001-09-13 2011-01-26 花王株式会社 Polyolefin resin composition
JP4781998B2 (en) * 2004-02-24 2011-09-28 株式会社カネカ Method for producing polyolefin pre-expanded particles using water as a foaming agent
WO2009001645A1 (en) * 2007-06-22 2008-12-31 Kaneka Corporation Polyolefin resin pre-foamed particle having antistatic property, and molded article produced from the particle
JP5372750B2 (en) * 2007-06-22 2013-12-18 株式会社カネカ Polyolefin resin pre-expanded particles having antistatic properties and molded articles obtained therefrom
JP2009215438A (en) * 2008-03-11 2009-09-24 Kaneka Corp Method for producing polypropylene-based resin pre-foamed particle
WO2013137411A1 (en) 2012-03-14 2013-09-19 株式会社カネカ Polypropylene resin foam particles, in-mold foam molded body comprising polypropylene resin foam particles, and method for producing same
US9611369B2 (en) 2012-03-14 2017-04-04 Kaneka Corporation In-mold foam molded body comprising polypropylene resin foam particles and method for producing same

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