JPS5930182B2 - resin composition - Google Patents

resin composition

Info

Publication number
JPS5930182B2
JPS5930182B2 JP4825576A JP4825576A JPS5930182B2 JP S5930182 B2 JPS5930182 B2 JP S5930182B2 JP 4825576 A JP4825576 A JP 4825576A JP 4825576 A JP4825576 A JP 4825576A JP S5930182 B2 JPS5930182 B2 JP S5930182B2
Authority
JP
Japan
Prior art keywords
silica gel
porous silica
hydrocarbon
resin composition
phr
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.)
Expired
Application number
JP4825576A
Other languages
Japanese (ja)
Other versions
JPS52130852A (en
Inventor
晋 「くれ」松
武 増井
久光 柿山
和男 池田
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.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
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 Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP4825576A priority Critical patent/JPS5930182B2/en
Publication of JPS52130852A publication Critical patent/JPS52130852A/en
Publication of JPS5930182B2 publication Critical patent/JPS5930182B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明はブロック共重合体に多孔性シリカゲルを配合し
てなるブロック共重合体組成物に関するもので、その目
的は樹脂本来の有する透明性及び印刷性を阻害すること
なく、シート及びフィルム状に成形した場合のシート及
びフィルムの滑り性(スリップ性)を附与したブロック
共重合体の樹脂組成物を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a block copolymer composition made by blending porous silica gel with a block copolymer. The present invention provides a block copolymer resin composition that imparts slip properties to sheets and films when molded into sheets and films.

スチレン系炭化水素と共役ジエン系炭化水素のブロック
共重合体のフィルム及びシートは、フィルム同志及びシ
ート同志の滑り性が悪いために、インフレーシヨン法で
フィルムを成形する際の開口性が悪く、そのためにダブ
ル状からシングル状にするのを困難にしたり(シングル
の巻取りが出来ない)更にダブル状で使用する時も口開
きが出来ないために実用に供し得ない欠点がある。
Films and sheets made of block copolymers of styrenic hydrocarbons and conjugated diene hydrocarbons have poor aperture properties when forming the film by the inflation method due to poor sliding properties between the films and between the sheets. This makes it difficult to convert a double shape into a single shape (single winding is not possible), and furthermore, when used in a double shape, the opening cannot be opened, making it impractical.

又、シートを二次加工してカップ、トレー等の容器とし
て使用する際、容器を積重ねておいて、上から1つ1つ
抜取つて容器に内容物を充填するときに、スリップ性が
ないために、容器の抜取り性(スタッカブル性)が悪く
、作業性を著しく悪くし、更にスリップ性不良は二次加
工するときにシートを成形機に送り込むときのトラブル
の大きな要因になつている。本発明は、スチレン系樹脂
自身のすぐれた透明性及び印刷性を保持しつつ、かかる
樹脂の欠点である滑り性(スリップ性)を改良した、ス
チレン系炭化水素と共役ジエン系炭化水素のブロック共
重合体組成物に関するものである。
In addition, when the sheets are processed into containers such as cups and trays, there is no slipping when the containers are stacked and pulled out one by one from the top to fill the containers. Furthermore, the container has poor removability (stackability), which significantly impairs workability, and poor slip properties are a major cause of trouble when feeding sheets into a molding machine during secondary processing. The present invention has developed a block combination of styrenic hydrocarbon and conjugated diene hydrocarbon that maintains the excellent transparency and printability of styrenic resin itself while improving the slipperiness, which is a drawback of such resin. The present invention relates to polymer compositions.

スチレン系炭化水素と共役ジエン系炭化水素のブロック
共重合体の滑性附与剤として脂肪酸アミド等の有機系滑
剤が用いられるが、有機系滑剤の場合は添加量を多く入
れても必ずしも滑性が十分でなく、インフレ時の開口性
が不十分であつたり真空成形容器のスタッカブル性が不
良である。
Organic lubricants such as fatty acid amides are used as lubricating agents for block copolymers of styrene hydrocarbons and conjugated diene hydrocarbons. is insufficient, the opening property during inflation is insufficient, and the stackability of the vacuum-formed container is poor.

又、添加量を多く入れると印刷インキの接着不良を起し
実用に供し難い。フ 本発明者はこの様な欠点を改良す
るために検討した結果、スチレン系炭化水素を50〜9
5wt%含有するスチレン系炭化水素と共役ジエン系炭
化水素からなるブロック共重合体に対して、細孔容積O
、Iml/ V以上でかつ平均粒径0.5〜20μを5
有する多孔性シリカゲルを0.01〜2PHR配合さ
せることにより、すぐれた滑性を附与しかつ樹脂自身の
持つすぐれた透明性及び印刷性を損わないことを見出し
た。
Moreover, if a large amount is added, poor adhesion of the printing ink will occur, making it difficult to put it to practical use. As a result of studies to improve these drawbacks, the present inventor found that styrenic hydrocarbons of 50 to 9
For a block copolymer containing 5 wt% of styrene hydrocarbon and conjugated diene hydrocarbon, the pore volume O
, Iml/V or more and an average particle size of 0.5 to 20 μ
It has been found that by blending 0.01 to 2 PHR of porous silica gel, it imparts excellent lubricity and does not impair the excellent transparency and printability of the resin itself.

この様なシリカゲルとしては富士デヴイソン化学K.K
.製サイロイド(商品名)等を上げることが出来る。本
発明に用いる多孔性シリカゲルは細孔容積が0.1d/
r以上の粒の表面積の大きいものが好ましく、0.11
1LI/7以下では実用上好ましい滑性を附与させない
As such silica gel, Fuji Davison Chemical K. K
.. It is possible to make products such as thyroid (product name). The porous silica gel used in the present invention has a pore volume of 0.1 d/
Preferably, particles with a large surface area of r or more, 0.11
If it is less than 1LI/7, practically preferable lubricity cannot be imparted.

又、細孔容積が0.1m1/r以上の多孔性シリカゲル
でも平均粒径が0.5μ以下では滑性不足となり、平均
粒径が20μ以上だと添加量を最低にしても得られたフ
イルム及びシートのヘイズが大きくなり透明性が悪くな
つて外観上好ましくない。
Furthermore, even if the porous silica gel has a pore volume of 0.1 m1/r or more, if the average particle size is less than 0.5 μm, the lubricity will be insufficient, and if the average particle size is 20 μm or more, the film obtained even if the amount added is the minimum. Also, the haze of the sheet increases and the transparency deteriorates, which is unfavorable in terms of appearance.

好ましい粒径範囲は0.7〜10μ、最も好ましい範囲
は1〜5μの範囲にある。多孔性シリカゲルの添加量は
、多過ぎると透明性に悪影響を及ぼし、少くな過ぎると
十分な滑性を附与しないことから0.01〜2PHRの
範囲で、好ましくは0.1〜0.3PHR1最も好まし
くは0.05〜1.0PHRの範囲で添加することが望
ましい。本発明においてプロツク重合体とは、スチレン
系炭化水素と共役ジエン系炭化水素を有機リチウム化合
物を重合開始剤としてプロツク状に共重合して得られる
樹脂でスチレン系炭化水素を50〜95wt%含む共重
合体である。
The preferred particle size range is 0.7 to 10 microns, and the most preferred range is 1 to 5 microns. The amount of porous silica gel added is in the range of 0.01 to 2 PHR, preferably 0.1 to 0.3 PHR, since too much will adversely affect transparency, and too little will not impart sufficient lubricity. Most preferably, it is added in a range of 0.05 to 1.0 PHR. In the present invention, a block polymer is a resin obtained by copolymerizing a styrene hydrocarbon and a conjugated diene hydrocarbon into a block shape using an organolithium compound as a polymerization initiator, and is a copolymer containing 50 to 95 wt% of a styrene hydrocarbon. It is a polymer.

ここでいうスチレン系炭化水素とはスチレン、α−メチ
ルスチレン等であり、共役ジエン系炭化水素はブタジエ
ン、イソプレン等である。プロツク共重合体に上記の多
孔性シリカゲルを添加するのは通常用いられるブレンド
方法、例えはプロツク共重合体と多孔性シリカゲルをペ
ンシェルミキサーで均一ブレンドして押出機にかける方
法等により行われる。
The styrenic hydrocarbons mentioned here include styrene, α-methylstyrene, etc., and the conjugated diene hydrocarbons include butadiene, isoprene, etc. The above-mentioned porous silica gel is added to the PROC copolymer by a commonly used blending method, for example, the PROC copolymer and porous silica gel are uniformly blended in a pen shell mixer, and the mixture is then passed through an extruder.

又、本発明の実施に当り、公知の帯電防止剤、安定剤、
滑剤、着色剤及び本発明のプロツク共重☆☆合体と相溶
性のある熱可塑性樹脂を添加しても何んらさしつかえな
い。
In carrying out the present invention, known antistatic agents, stabilizers,
There is nothing wrong with adding a lubricant, a coloring agent, and a thermoplastic resin that is compatible with the block copolymer of the present invention.

以下更に実施例を以つて本発明を説明する。The present invention will be further explained below with reference to Examples.

実施例 1スチレン〜ブタジエン〜スチレンのプロツク
構造を有し、スチレンを80wt%含むプロツク共重合
体に対して各種多孔性シリカゲルをペンシェルミキサー
で十分均一に混合しこれを押出機にかけて、ペレツト状
にし、次いで65′押出機にてインフレシヨン法により
成膜し、厚さ25μのフイルムを製造した。
Example 1 A block copolymer having a block structure of styrene-butadiene-styrene and containing 80 wt% styrene was sufficiently uniformly mixed with various porous silica gels using a pen shell mixer, and then put into an extruder to form pellets. Then, a film was formed using an inflation method using a 65' extruder to produce a film with a thickness of 25 μm.

得られたフイルムの開口性、滑り角度、Hazel印刷
性を表1に示す。
Table 1 shows the opening property, sliding angle, and Hazel printability of the obtained film.

表1は細孔容積0.1m1/y以上で、かつ平均粒径0
.5〜20μの多孔性シリカゲルを0.01〜2PHR
添加することにより開口性、滑り性を有し、樹脂の透明
性、印刷性を阻害しないことを示している。実施例 2 実施例1と同じ樹脂に多孔性シリカゲル(細孔容積1.
6m2/r、平均粒径3.2μ)を0.3PHR添加し
ペンシェルミキサーで混合し、これを押出機にかけてペ
レツト状にし、次いでT−ダイ法により0.3%厚さの
シートを得た。
Table 1 shows that the pore volume is 0.1 m1/y or more and the average particle size is 0.
.. 0.01-2PHR of 5-20μ porous silica gel
It has been shown that the addition of this compound provides openability and slipperiness, and does not impede the transparency and printability of the resin. Example 2 Porous silica gel (pore volume 1.
6m2/r, average particle size 3.2μ) was added at 0.3PHR and mixed using a pen shell mixer, which was made into pellets using an extruder, and then a sheet with a thickness of 0.3% was obtained using the T-die method. .

得られたシートのシート同志の滑り角度及び透明性を測
定した。
The sliding angle between the sheets and the transparency of the obtained sheet were measured.

更にこのシートをイリヒ社製の単発、真空成形機にて1
00CCの丸カツプを作りスタツカブル性を調べた。
This sheet is then processed into a single-shot vacuum forming machine manufactured by Illich.
A round cup of 00CC was made and its stackability was investigated.

比較の為に多孔性シリカゲルを添加しない樹脂について
も同様の試験をした。
For comparison, a similar test was conducted on a resin to which no porous silica gel was added.

Claims (1)

【特許請求の範囲】[Claims] 1 スチレン系炭化水素を50〜90wt%含有するス
チレン系炭化水素と共役ジエン系炭化水素からなるブロ
ック共重合体に対して、細孔容積0.1ml/g以上で
かつ平均粒径0.5〜20μを有する多孔性シリカゲル
を0.01PHR〜2.00PHR配合してなる樹脂組
成物。
1 For a block copolymer consisting of a styrenic hydrocarbon and a conjugated diene hydrocarbon containing 50 to 90 wt% of styrenic hydrocarbon, the pore volume is 0.1 ml/g or more and the average particle size is 0.5 to A resin composition containing 0.01 PHR to 2.00 PHR of porous silica gel having a diameter of 20 μ.
JP4825576A 1976-04-27 1976-04-27 resin composition Expired JPS5930182B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4825576A JPS5930182B2 (en) 1976-04-27 1976-04-27 resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4825576A JPS5930182B2 (en) 1976-04-27 1976-04-27 resin composition

Publications (2)

Publication Number Publication Date
JPS52130852A JPS52130852A (en) 1977-11-02
JPS5930182B2 true JPS5930182B2 (en) 1984-07-25

Family

ID=12798323

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4825576A Expired JPS5930182B2 (en) 1976-04-27 1976-04-27 resin composition

Country Status (1)

Country Link
JP (1) JPS5930182B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06855B2 (en) * 1986-04-12 1994-01-05 電気化学工業株式会社 Styrenic resin stretch sheet
JPH06856B2 (en) * 1986-04-16 1994-01-05 電気化学工業株式会社 Styrenic resin stretch sheet
US4814364A (en) * 1987-03-05 1989-03-21 Nippon Steel Chemical Co., Ltd. Inorganic porous substance containing resin composition

Also Published As

Publication number Publication date
JPS52130852A (en) 1977-11-02

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