JPH0286640A - Styrenic resin composition - Google Patents

Styrenic resin composition

Info

Publication number
JPH0286640A
JPH0286640A JP23629688A JP23629688A JPH0286640A JP H0286640 A JPH0286640 A JP H0286640A JP 23629688 A JP23629688 A JP 23629688A JP 23629688 A JP23629688 A JP 23629688A JP H0286640 A JPH0286640 A JP H0286640A
Authority
JP
Japan
Prior art keywords
mold release
resin composition
styrenic resin
present
mold
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
JP23629688A
Other languages
Japanese (ja)
Inventor
Eiji Kamiryo
英二 上領
Ichiro Sohara
曽原 一郎
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.)
Riken Vitamin Co Ltd
Original Assignee
Riken Vitamin 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 Riken Vitamin Co Ltd filed Critical Riken Vitamin Co Ltd
Priority to JP23629688A priority Critical patent/JPH0286640A/en
Publication of JPH0286640A publication Critical patent/JPH0286640A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は成形時に良好な離型性を発揮するスチレン系樹
脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a styrenic resin composition that exhibits good mold release properties during molding.

(従来の技術及び発明が解決しようとする課題)スチレ
ン系樹脂を射出成形、押出成形あるいはその他の成形法
により樹脂を成形する場合、樹脂と金属表面との離型性
が不充分の時には、成形品が金型に付着したり、表面に
すしが入ったりして、生産性の低下あるいは成形品の変
形あるいは表面不良等の問題点が発生する。
(Prior art and problems to be solved by the invention) When molding styrene resin by injection molding, extrusion molding, or other molding methods, when the mold releasability between the resin and the metal surface is insufficient, the molding Problems such as a decrease in productivity, deformation of the molded product, or surface defects occur due to the product adhering to the mold or staining on the surface.

この為、この様な離型性不足に原因するトラブルを防止
する手段として、一般には、1)金型面への離型剤の塗
布、2)樹脂中への離型剤の添加(以下内部添加という
)の方法か採られている。1)の方法の離型剤としては
、溶剤希釈あるいはエマルション系のシリコーンオイル
がよく使用されているが、溶剤による環境汚染あるいは
残留シリコーンオイルの後工程への悪影響、例えば着色
不良などの欠点を有している。2)の内部添加離型剤と
しては、例えば特開昭54−132650号では高級脂
肪酸及び/又は同金属塩とグリセリンモノステアレート
の組み合わせが、又特開昭59−68357号では、高
級脂肪酸及び/又は同金属塩とN−アルキル脂肪酸アマ
イドの組み合わせが示されている。又用途によっては、
金属性化合物を嫌う場合が、例えばP[^5TIC3E
ngineering / September ’8
7.33〜34にはABS用ノレノンメタリック脂肪化
学系離型剤てセチルステアレート、セチルパルミテート
が有効であることが示されている。しかし概して、これ
らのものは、実際上必要な離型性を得るためには多量の
添加を強いられ、その影響が成形品の熱変形温度の低下
となって現われるという欠点を有する。従って内部添加
法においては、少量で効果を発揮し、かつ非金属性化合
物であることが望まれている。
For this reason, as a means to prevent troubles caused by such insufficient mold release properties, the following methods are generally used: 1) Applying a mold release agent to the mold surface, 2) Adding a mold release agent to the resin (hereinafter referred to as internal A method called "addition" is adopted. Solvent-diluted or emulsion-based silicone oil is often used as a mold release agent in method 1), but it has disadvantages such as environmental pollution due to the solvent and adverse effects on subsequent processes of residual silicone oil, such as poor coloring. are doing. As the internally added mold release agent in 2), for example, in JP-A-54-132650, a combination of higher fatty acids and/or their metal salts and glycerin monostearate is used, and in JP-A-59-68357, higher fatty acids and A combination of the same metal salt and an N-alkyl fatty acid amide is shown. Also, depending on the use,
If you dislike metallic compounds, for example, P[^5TIC3E
ngineering / September '8
7.33-34 show that cetyl stearate and cetyl palmitate are effective as nolenone metallic fatty chemical mold release agents for ABS. However, in general, these materials have the disadvantage that they must be added in large amounts in order to obtain the practically necessary mold release properties, and the effect of this is a decrease in the heat distortion temperature of the molded article. Therefore, in the internal addition method, it is desired that the compound be effective in a small amount and be non-metallic.

本発明の目的は、上記問題点が解決された内部添加用離
型剤を見い出し、ひいては離型性のすぐれたスチレン樹
脂系組成物を提供することである。
An object of the present invention is to find a mold release agent for internal addition that solves the above-mentioned problems, and to provide a styrene resin composition with excellent mold release properties.

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは、成形品の熱変形温度の低下に影響の出な
い低い添加量で離型性を発揮し且つ非金属性化合物であ
る内部添加離型剤について鋭意検討した結果、長鎖α−
オレフィンエポキシド(以下AOEと略記〉が本発明の
目的に合致する内部添加@型剤であることを見い出し、
本発明を完成するに至った。
The present inventors have conducted intensive studies on an internally added mold release agent that is a non-metallic compound and exhibits mold release properties at a low additive amount that does not affect the reduction of the heat distortion temperature of the molded product. −
We have discovered that olefin epoxide (hereinafter abbreviated as AOE) is an internally added mold agent that meets the purpose of the present invention,
The present invention has now been completed.

本発明で使用される長鎖AOEは、エチレンを低重合し
て)qられる長鎖α−オレフィンの末端二重結合を酸化
してエポキシドとした化合物である。
The long-chain AOE used in the present invention is a compound obtained by oxidizing the terminal double bond of a long-chain α-olefin (by low polymerization of ethylene) to form an epoxide.

本発明で使用される長鎖AOEの炭素数は12以上、好
ましくは、20以上である。炭素数が12より少ないと
、離型効果はあるものの、低沸点の為に加工中揮発した
り、熱変形温度を下げたりして好ましくない。また長鎖
AOEは、既知の内部添加離型剤、例えば、脂肪酸金属
塩、エチレンビス脂肪酸アマイド、グリセリンモノステ
アレート等と併用使用しても本発明の目的に合致する。
The long-chain AOE used in the present invention has 12 or more carbon atoms, preferably 20 or more carbon atoms. If the number of carbon atoms is less than 12, although it has a mold release effect, it is not preferable because it volatilizes during processing due to its low boiling point or lowers the heat distortion temperature. Furthermore, long-chain AOE can also be used in combination with known internally added mold release agents, such as fatty acid metal salts, ethylene bis fatty acid amide, glycerin monostearate, etc., to meet the objectives of the present invention.

本発明においてスチレン系樹脂とは、重合体構成成分と
して、スチレン、メチルスチレンを持つ重合体であり、
例えばポリスチレン、ABS、As等が挙げられるが、
これらだけに限るものではない。
In the present invention, the styrenic resin is a polymer having styrene and methylstyrene as polymer constituents,
Examples include polystyrene, ABS, As, etc.
It is not limited to these.

〔実施例〕〔Example〕

次に実施例をもって本発明の有効性を具体的に示す。 Next, the effectiveness of the present invention will be specifically demonstrated with examples.

一離型性の評価方法 ■樹脂(ABS、ポリスチレンあるいはAs)と離型剤
の規定量をプラストミルを用いて、190℃−8分間混
練し、その俊、テフロンコーティングしたプレス板を用
いて、170’C−100Kg/ cttt −3分の
条件で1#厚シートにする。
1. Method for evaluating mold release properties ■ A specified amount of resin (ABS, polystyrene, or As) and mold release agent were kneaded using a plastomill at 190°C for 8 minutes, and then kneaded at 170°C using a Teflon-coated press plate. 'C - Make a 1# thick sheet under the conditions of 100Kg/cttt -3 minutes.

■IM厚シートから、コルクポーラ(N(17)を用い
て直径12履の円形試料を採取する。
■Collect a circular sample with a diameter of 12 pieces from the IM thick sheet using a cork polar (N (17)).

■クロムメツキ加工した標準試験板 2.OX25x1
00 m/m 2枚をクロスさせた中央部に円形試料を
サンドイッチし、180 ’C−1ON!9/ ct/
を一8分の条件でプレスし、試験板を圧着する。
■Chrome-plated standard test plate 2. OX25x1
00 m/m A circular sample was sandwiched in the center of two crossed sheets, and 180'C-1ON! 9/ct/
was pressed for 18 minutes to crimp the test plate.

■圧着した2枚のクロムメツキ標準試験板をショツパー
型引張り試験機にセットし、200#/minの速度で
引張り、2枚のクロムメツキ標準試験板を引き離すに要
する力(剥離力)を測定する。
(2) Set the two crimped standard chrome plated test plates in a Schopper type tensile tester, pull at a speed of 200 #/min, and measure the force (peel force) required to separate the two standard chrome plated test plates.

一評価結果− EBS=エチレンビススビスロアミド GMS=グリセリンモノスデアレート AOE16B =炭素数16〜18のα−オレフィンエ
ポキシドA OE 208−炭素数20〜28のα−オ
レフィンエポキシドA OE 300−炭素数30以上
のα−オレフィンエポキシド表2 PS*7.As*8の場合 *7 PS=三井東圧化学製1−一ポレックスGP55
5承8AS=三井東圧化学製ライタツクA120PC〔
発明の効果〕 表11表2の比較例1〜10及び本発明品1〜10の剥
離力の数値の比較により、本発明品は、その添加量が既
存品の172以下においても同等もしくはそれ以上の剥
離力すなわち離型を促進する機能を示すことは明らかで
ある。
One evaluation result - EBS = Ethylene bis bisthroamide GMS = Glycerin monosdaleate AOE16B = α-olefin epoxide A having 16 to 18 carbon atoms OE 208 – α-olefin epoxide A having 20 to 28 carbon atoms OE 300 – 30 carbon atoms Above α-olefin epoxide Table 2 PS*7. In the case of As*8*7 PS=Mitsui Toatsu Chemical 1-1 Polex GP55
5.8AS = Mitsui Toatsu Chemical Light Tack A120PC [
[Effect of the invention] Comparison of the numerical values of peeling force of Comparative Examples 1 to 10 and Inventive Products 1 to 10 in Table 11 and Table 2 shows that the inventive product is equivalent to or greater than the existing product even when the amount added is 172 or less. It is clear that the material exhibits a peeling force, that is, a function of promoting mold release.

Claims (1)

【特許請求の範囲】[Claims] (1)α−オレフィンエポキシドを必須成分として含む
ことを特徴とするスチレン系樹脂組成物。
(1) A styrenic resin composition characterized by containing an α-olefin epoxide as an essential component.
JP23629688A 1988-09-22 1988-09-22 Styrenic resin composition Pending JPH0286640A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23629688A JPH0286640A (en) 1988-09-22 1988-09-22 Styrenic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23629688A JPH0286640A (en) 1988-09-22 1988-09-22 Styrenic resin composition

Publications (1)

Publication Number Publication Date
JPH0286640A true JPH0286640A (en) 1990-03-27

Family

ID=16998690

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23629688A Pending JPH0286640A (en) 1988-09-22 1988-09-22 Styrenic resin composition

Country Status (1)

Country Link
JP (1) JPH0286640A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS502759A (en) * 1973-05-10 1975-01-13
JPS57135851A (en) * 1981-02-16 1982-08-21 Daicel Chem Ind Ltd Resin composition
JPS58109556A (en) * 1981-12-23 1983-06-29 Idemitsu Petrochem Co Ltd Plasticizer for synthetic resin

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS502759A (en) * 1973-05-10 1975-01-13
JPS57135851A (en) * 1981-02-16 1982-08-21 Daicel Chem Ind Ltd Resin composition
JPS58109556A (en) * 1981-12-23 1983-06-29 Idemitsu Petrochem Co Ltd Plasticizer for synthetic resin

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