JPS58217541A - Low-temperature impact-resistant resin composition - Google Patents

Low-temperature impact-resistant resin composition

Info

Publication number
JPS58217541A
JPS58217541A JP10044982A JP10044982A JPS58217541A JP S58217541 A JPS58217541 A JP S58217541A JP 10044982 A JP10044982 A JP 10044982A JP 10044982 A JP10044982 A JP 10044982A JP S58217541 A JPS58217541 A JP S58217541A
Authority
JP
Japan
Prior art keywords
vinyl chloride
parts
resin
weight
resin composition
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
JP10044982A
Other languages
Japanese (ja)
Inventor
Akio Koyama
明夫 小山
Yuichi Kojima
裕一 小島
Kaoru Ozawa
小沢 薫
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.)
PLUS TEKU KK
Original Assignee
PLUS TEKU 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 PLUS TEKU KK filed Critical PLUS TEKU KK
Priority to JP10044982A priority Critical patent/JPS58217541A/en
Publication of JPS58217541A publication Critical patent/JPS58217541A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide a vinyl chloride resin compns. exhibiting excellent impact resistance at low temp., by adding an impact modifier and a processing aid. CONSTITUTION:100pts.wt. vinyl chloride resin such as a graft copolymer obtd. from vinyl chloride and an ethylene/vinyl acetate copolymer, 5-25pts.wt. impact modifier, pref. based on an acrylic resin, and 0.5-20pts.wt. olefin processing aid such as an ethylene/alpha-olefin copolymer, are blended together.

Description

【発明の詳細な説明】 本発明は低温耐衝撃性樹脂組成物、詳しくは低温におい
てすぐれた耐衝撃性を示す塩化ビニル系の樹脂組成物に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a low-temperature impact-resistant resin composition, and more particularly to a vinyl chloride-based resin composition that exhibits excellent impact resistance at low temperatures.

塩化ビニル系樹脂の耐衝撃性を向上″rるため、スチレ
ン−ブタジェンゴム(SDR) 、ポリブタジェン−ア
クリルニトリル−スチレンのグラフト重合イ本(八BS
) 、ポリブタジェン−メチルメタクリレート−スチレ
ンのグラフト重合体(MBS)などブタジェン系切崩を
M礎トfるもの、ポリエチレン(PE)、塩素化ポリエ
チレン(CPE) 、エチレン−酢酸ビニルの共重合体
<Evh)などポリオレフィン系樹脂を基礎とするもの
、アクリル酸エステル系114脂(RA)。
In order to improve the impact resistance of vinyl chloride resin, styrene-butadiene rubber (SDR) and polybutadiene-acrylonitrile-styrene graft polymerization (8BS
), polybutadiene-methyl methacrylate-styrene graft polymers (MBS) and other butadiene-based truncation polymers, polyethylene (PE), chlorinated polyethylene (CPE), ethylene-vinyl acetate copolymers <Evh ), those based on polyolefin resins, and acrylic acid ester-based 114 resins (RA).

メタクリル酸エステル系樹脂(RFvLA )などアク
リル系樹脂を基礎とするものを耐衝撃性向上剤に用いろ
ことはよく知られている。
It is well known that acrylic resin-based materials such as methacrylic acid ester resins (RFvLA) should be used as impact resistance improvers.

しかしながら、これら耐衝撃性向上用の改質剤を含有さ
せた塩化ビニル系樹脂組成物の成形品は常温以上ではほ
ぼ期待した耐衝撃性が得られろか、低温では耐@撃性が
著しく劣化し1例えば農業用支柱、道路用支柱のように
屋外で使用するときは冬期に僅かなWi撃的外力でも割
れなどを生じ、′9.冷地または低湿雰囲気での実用に
は雑煮があった。
However, molded products made from vinyl chloride resin compositions containing modifiers for improving impact resistance do not have the expected impact resistance above room temperature, but their impact resistance significantly deteriorates at low temperatures. 1. For example, when used outdoors such as agricultural props and road props, even a slight external force may cause cracks in the winter.'9. Zoni was used in practical applications in cold regions or low humidity environments.

本発明はこのような問題なW¥決し、特に低温ておいて
でぐれた耐衝撃性を示τ例脂組成物を提1aすることを
目〔月として発B月さねたもので、塩化ビニル系樹脂に
酎(勺−1性向上剤およびオレフィン系加工助丼1を格
加してなることシ朽徴と−tろものである。
The purpose of the present invention is to avoid such problems and to provide a tau resin composition that exhibits excellent impact resistance, especially when kept at low temperatures. It is made by adding a property improver (1) and an olefin-based processing aid (1) to a vinyl resin.

本発明において、塩化ビニル系樹l旨としては塩化ビニ
ル樹脂のほかに塩化ビニルと酢酸ビニル、エチレンプロ
ピレン、塩化ビニリチン、アクリル酸二ステル等との共
重合体が例示されろが、特にエチレン−酢酸ビニル共重
合体と塩化ビニルとのグラフト重合体(EVA−pvc
)はそれ自身かなりの低温耐衝13件を有しているので
本発明に好ましい材料である。
In the present invention, examples of the vinyl chloride resin include copolymers of vinyl chloride and vinyl acetate, ethylene propylene, vinylitine chloride, dister acrylate, etc., in addition to vinyl chloride resin, but in particular, ethylene-acetic acid Graft polymer of vinyl copolymer and vinyl chloride (EVA-pvc
) is a preferred material for the present invention because it itself has considerable low temperature impact resistance.

また、塩化ビニル樹脂にEVAを併用した系。Also, a system that uses EVA in combination with vinyl chloride resin.

エチレン−塩化ビニル共重合体CP(VC−E))にE
VAを併用した系などもEVA−PVCと近似の物理的
性質を有しているので本発明の塩化ビニル系明脂として
好適である。
Ethylene-vinyl chloride copolymer CP (VC-E))
Systems using VA in combination have physical properties similar to those of EVA-PVC, and are therefore suitable as the vinyl chloride-based bright resin of the present invention.

尚1本発明においては前述のような塩化ビニル系樹脂か
ら適宜選ばれた一種また番よ74以上が使用され、更に
外部υ+ll剤のほかに必要により熱安だ剤、fi剤、
酸化防止剤、紫外線吸収剤、無機充填剤、難燃剤を加え
ろことができる。
In addition, in the present invention, one type or number 74 or more appropriately selected from the above-mentioned vinyl chloride resins is used, and in addition to the external υ+ll agent, if necessary, a heat stabilizer, a fi agent,
Antioxidants, UV absorbers, inorganic fillers, and flame retardants can be added.

次に、耐衝撃性向上剤として本発明では先に述べ1こよ
うなブタCエン系側脂、ポリオレフィン系樹脂、アクリ
ル系樹脂を基礎とする既知のものを使用するが、アクリ
ル系樹脂を基礎とするものが好適である。捷だ1本発明
では一種または二種以上の耐衝撃性向上剤を選んで用い
ろことができるが、塩化ビニル系樹脂100取量部に対
し1〜50重量部、好ましくは5〜25市量部の範囲で
加えろ。
Next, in the present invention, as impact resistance improvers, known ones based on buta-C-ene type side fats, polyolefin resins, and acrylic resins as mentioned above are used. It is preferable that In the present invention, one or more types of impact resistance improvers can be selected and used, but 1 to 50 parts by weight, preferably 5 to 25 parts by weight per 100 parts of vinyl chloride resin. Please add as much as possible.

更に、耐衝撃性向上剤とともに塩化ビニル系樹脂に加え
るオVフィ/系加工助剤としてはエチレン−αオレフイ
ン共重合体(α−Et)その他の共重合体或いはオレフ
ィン系樹脂ト他物質との混合物を使用する。オレフィン
系JJO工助剤も一1重または二種以上を選んで用いろ
ことができ、塩化ビニル系樹脂100重量部に対し01
〜30重量部、好ましくは05〜20重量部の範囲で加
えろ。
Furthermore, as an ophthalmic processing aid added to the vinyl chloride resin together with the impact resistance improver, ethylene-α-olefin copolymer (α-Et) and other copolymers, or combinations of olefin resin and other substances can be used. Use a mixture. Olefin-based JJO processing aids can also be used in combinations of 11 or 2 or more.
Add in the range of ~30 parts by weight, preferably 05-20 parts by weight.

次に本発明の比較列と実施列の試験結果を述べる。Next, the test results of the comparative column and the practical column of the present invention will be described.

試験A−1からA−6を通じて試料は各混合物な8イン
チのテストロールによる混練す(ロール17爪度150
〜160℃1巻付き後5分間混練り)を行って素糾すシ
ートを作り、これをプレス成彩(温度180℃1時間1
0分間、最大圧−力120に&) して平滑な厚さ5藺
のシートとし。
Throughout Tests A-1 to A-6, each sample was kneaded with an 8-inch test roll (roll 17, 150 mm).
~ 160℃ (1 roll and kneading for 5 minutes) to make a sheet to be kneaded, press coloring (temperature 180℃ for 1 hour 1 hour)
Press at a maximum pressure of 120°C for 0 minutes to form a smooth sheet with a thickness of 5cm.

切削IJII工によりJIS K−7111に準するテ
ストピースに成形した。試験はシャルピーf′i撃UC
験機でJIS K−7111に依って行い、テストピー
スは所定温IWで試験されるように考慮して加熱または
冷却した。尚、各試験のアクリル系改質剤、アクリル系
加工助剤、オレフィン系加工助剤はそれぞれ商品名フレ
j) HIA28.メタブレンP501 、タフマーP
O680を使用した。
A test piece conforming to JIS K-7111 was formed by cutting IJII machining. The exam is Charpy f'i attack UC
The test was conducted using a testing machine in accordance with JIS K-7111, and the test piece was heated or cooled so that it would be tested at a predetermined temperature IW. In addition, the acrylic modifier, acrylic processing aid, and olefin processing aid used in each test are each under the trade name Frej) HIA28. Metablen P501, Tafmar P
O680 was used.

〔試験A−1) 塩化ビニル系樹脂としてEVA−PvCQ中から東洋曹
達工業製商品名ハイレジンH−130(al。
[Test A-1] As a vinyl chloride resin, Hi-Resin H-130 (trade name, manufactured by Toyo Soda Kogyo Co., Ltd.) (al) was selected from EVA-PvCQ.

H−120(bl、  H−110(cl、  EVA
を40%含むもの(d)。
H-120 (bl, H-110 (cl, EVA
Containing 40% (d).

P(VC−Eンの中からエチレンを4憾含み;= s 
o 。
P (contains 4 ethylene from VC-E; = s
o.

Oもの(elおよびp=1000のLJA化ビエビニル
樹脂lを用い、各100重量部に鉛系安定剤5重液部。
(Using LJA bivinyl resin 1 with el and p = 1000, 5 heavy liquid parts of lead-based stabilizer for each 100 parts by weight.

アクリル系改質剤7.5重量部、アクリル系加工助剤1
.5重激部、オレフイ/糸1J11工助剤3重量部を加
えたテストヒースの衝槃頭(23’C。
7.5 parts by weight of acrylic modifier, 1 part of acrylic processing aid
.. Test heath ram head (23'C.

−10℃)および残イヘ(−1o℃)は次表σ)通りで
ある。
-10°C) and residual temperature (-10°C) are as shown in the following table σ).

〔試験人−2〕 塩化ビニル系樹脂として部品名ハイレジンH−130を
用いその100重量部にアクリル系改質剤7.5重量部
を加えたものに鉛系安定剤。
[Test Person-2] A lead-based stabilizer was prepared by adding 7.5 parts by weight of an acrylic modifier to 100 parts by weight of HiResin H-130 as the vinyl chloride resin.

錫系安定剤、オレフィン系加工助剤を適宜添加したテス
トピースの衝撃値(23℃、−10℃)および残率(−
10℃)は次表の通りである。
Impact value (23℃, -10℃) and residual rate (-
10°C) are as shown in the following table.

〔試験A−3〕 塩化ビニル系樹脂として商品名ハイレジンH−130を
用い、その100重量部に鉛系安定剤5取量部、アクリ
ル系加工助剤1.5重量部。
[Test A-3] Hiresin H-130 (trade name) was used as the vinyl chloride resin, and 5 parts by weight of lead stabilizer and 1.5 parts by weight of acrylic processing aid were added to 100 parts by weight of the vinyl chloride resin.

オレフィン系加工助剤3重量部を加えたものに耐衝撃向
上用のアクリル糸数η31(at 、ブタl;1ン系改
質剤のABSから商品名ブレンデイツクス301(bl
およびMBSから商品名カネエースB22[cl、オレ
フィン系改質剤のCPEから商品名グイソラツクG−2
45(diおよびEVA−PVCから商品名TG−40
telな七れぞれ添加したテストピースの衝撃値(23
℃、−10℃)および残率(−10℃)は次表の苅りで
ある。
3 parts by weight of an olefin-based processing aid is added to the acrylic yarn number η31 (at, 1; 1) to which 3 parts by weight of an olefin-based processing aid is added.
From MBS, the product name is Kane Ace B22 [cl; from the olefinic modifier CPE, the product name is Gusolac G-2.
45 (product name TG-40 from di and EVA-PVC
The impact value of the test piece to which each of the seven substances was added (23
℃, -10℃) and residual rate (-10℃) are shown in the following table.

〔試験A−4〕 塩化ビニル系樹脂として塩化ビニル樹脂に=1000)
 (lo重蹴部にEVA (商品名エルパロイ843)
10重量部を併用した系に鉛系安定剤5重量部、アクリ
ル系加工助剤1.5重量部を加えたものにアクリル系改
質剤、オレフィン系加工助剤を適宜添加したテストピー
スの衝撃値(23℃、−10℃)および残率(−10℃
)は次表の通りである。
[Test A-4] Vinyl chloride resin as vinyl chloride resin = 1000)
(EVA for lo heavy kick part (product name Elpaloy 843)
Impact of a test piece prepared by adding 10 parts by weight of a lead-based stabilizer, 1.5 parts by weight of an acrylic processing aid, an acrylic modifier, and an olefin processing aid as appropriate. Value (23℃, -10℃) and residual rate (-10℃
) are shown in the table below.

〔試験A−5〕 塩化ビニル系樹脂として部品名ハイレジント130を用
いその100重量部圧鉛系豪邸剤5重量部、アクリル系
加工助剤1.5重量部な加えたものにアクリル系改質剤
、オレフィン系加工助剤を・商宜添vuシたテストピー
スの衝撃値(23’C,−10℃)J−:よび残h: 
(−10’C) +i r表の辿りである。
[Test A-5] Using the part name Hi-Resist 130 as the vinyl chloride resin, 100 parts by weight of the resin, 5 parts by weight of a pressurized lead agent, and 1.5 parts by weight of an acrylic processing aid were added to the acrylic modifier. , Impact value (23'C, -10°C) of test piece with olefinic processing aid and commercial additive added: J-: and residual h:
(-10'C) +i This is a trace of the r table.

〔試験A−6〕 塩化ビニル系樹脂として商品名・・イレC/H−130
を甲いその100−円量ド1)に鉛系安定剤5重量部、
アクリル系加工助剤1.s fit部、アクリル系改質
剤7.5重量部を加えたものにオレフィン系加工助剤を
添加景を変えて添加したテストピースの衝撃値(23℃
、−1O℃)および残率(−10C)は次表の通りであ
る。
[Test A-6] As a vinyl chloride resin, trade name: Ire C/H-130
5 parts by weight of lead-based stabilizer to the 100-yen amount 1),
Acrylic processing aid 1. Impact value of test pieces (23°C
, -10C) and residual rate (-10C) are shown in the following table.

〔試験B〕[Test B]

次に、試料を前記各試験と同一方法でJISK−711
0にりするテストピースに成形し、アイゾツト試験機で
JIS K−7110に依る試験を行った。本発明酩は
商品名ハイレジンH−130の100市量部に鉛系安定
剤5重量部、鈷糸安定剤0.5屯h(部、アクリル系改
質剤7.5市量部。
Next, the sample was tested according to JISK-711 in the same manner as in each of the above tests.
The sample was molded into a test piece having a value of 0, and tested in accordance with JIS K-7110 using an Izot tester. The present invention contains 100 parts by weight of the product name Hi-Resin H-130, 5 parts by weight of a lead-based stabilizer, 0.5 ton h (parts) of a cord stabilizer, and 7.5 parts by weight of an acrylic modifier.

アクリル糸加工助剤1 、5 il、”m部tvよびオ
レフィン系加工助剤3重量部をjJDえたもの、比較品
1は部品名ハイレジンH−130の100重量部に錫系
安定剤6型景部、アクリル糸改質剤15ME ft部、
を加えたもの、比較品2は塩化ビニル樹脂(i;=to
oo)の100重駐重圧鉛系安定毘5重豪邸、アクリル
系改質剤15重計部、アクリル系加工助剤1.5重量部
を加えたもので、各画定温度におけろ衝撃値、残率は次
表の通りである。
Comparative product 1 contains 100 parts by weight of part name Hi-Resin H-130 and 6 parts by weight of tin-based stabilizer. part, acrylic yarn modifier 15ME ft part,
Comparative product 2 is vinyl chloride resin (i;=to
oo), 100-weight lead-based stabilizer, 15 weight parts of acrylic modifier, and 1.5 parts by weight of acrylic processing aid were added, and the shock value at each defined temperature, The remaining rates are shown in the table below.

以上の試該結果から、塩化ビニル系樹脂として塩化ビニ
ル樹脂単独よりも塩化ビニルを幹樹脂とするグラフト重
合体寸たは共重合体或いはEVAを併用した系などの方
が好ましいこと、および耐衝撃性向上剤と・七てアクリ
ル系改質剤が好ましいこと、更に塩化ビニル系樹脂の種
類、改質剤などの種類および添加量に心じてオレフィン
系71υ工助剤の適正量をユベ定して加えることにより
低温における耐衝撃性が飛躍的に向上子ろことが判シ)
From the above test results, it is clear that as a vinyl chloride-based resin, it is preferable to use a graft polymer or copolymer with vinyl chloride as the main resin, or a system in which EVA is used in combination, rather than vinyl chloride resin alone, and to improve impact resistance. The appropriate amount of the olefin-based 71υ processing aid is determined based on the fact that acrylic-based modifiers are preferred as property improvers, and the type and amount of vinyl chloride resin, modifier, etc. By adding this, the impact resistance at low temperatures is dramatically improved.)
.

代理人野沢睦秋Agent Mutsuaki Nozawa

Claims (1)

【特許請求の範囲】 (11塩化ビニル系樹脂に耐衝撃性向上剤およびオレフ
ィン系加工助剤を添加してなることを特徴とする低温耐
衝撃性樹脂組成物。 (2)塩化ビニル系樹脂がエチレン−酢酸ビニル共重合
体と塩化ビニルとのグラフzt合体である特許請求の範
囲(1)に記載の樹脂組成物。 (3)塩化ビニル系樹脂が塩化ビニル樹脂にエチレン−
酢酸ビニル共重合体を併、用した系である特許請求の範
囲(1)に記載の樹脂組成物。 (4)塩化ビニル系樹脂がエチレン−塩化ビニル共重合
体にエチレン−酢酸ビニル共重合体を併用した系であろ
% iFF請求の範囲(1)に記載の樹脂組成物。 (5)耐衝撃性向上剤がアクリル系樹脂を基礎とする改
質剤である特許請求の範囲(1)に記載の樹脂組成物。 (6)塩化ビニル系樹脂100重量部に耐衝撃性向上剤
5〜25重量部およびオレフィン系加工助剤O,S〜2
0重量部を添加した特許請求の範囲(1)に記載の樹脂
組成物。
[Scope of Claims] (11) A low-temperature impact resistant resin composition characterized by adding an impact resistance improver and an olefin processing aid to a vinyl chloride resin. (2) A vinyl chloride resin The resin composition according to claim (1), which is a graph zt combination of an ethylene-vinyl acetate copolymer and vinyl chloride. (3) The vinyl chloride resin is a vinyl chloride resin mixed with ethylene-
The resin composition according to claim (1), which is a system in which a vinyl acetate copolymer is also used. (4) The resin composition according to claim (1), in which the vinyl chloride resin is a combination of an ethylene-vinyl chloride copolymer and an ethylene-vinyl acetate copolymer. (5) The resin composition according to claim (1), wherein the impact resistance improver is a modifier based on an acrylic resin. (6) 100 parts by weight of vinyl chloride resin, 5 to 25 parts by weight of impact resistance improver and 2 to 2 parts of olefin processing aid O, S
The resin composition according to claim (1), in which 0 parts by weight is added.
JP10044982A 1982-06-11 1982-06-11 Low-temperature impact-resistant resin composition Pending JPS58217541A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10044982A JPS58217541A (en) 1982-06-11 1982-06-11 Low-temperature impact-resistant resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10044982A JPS58217541A (en) 1982-06-11 1982-06-11 Low-temperature impact-resistant resin composition

Publications (1)

Publication Number Publication Date
JPS58217541A true JPS58217541A (en) 1983-12-17

Family

ID=14274219

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10044982A Pending JPS58217541A (en) 1982-06-11 1982-06-11 Low-temperature impact-resistant resin composition

Country Status (1)

Country Link
JP (1) JPS58217541A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5157751A (en) * 1974-11-16 1976-05-20 Mitsubishi Monsanto Chem HORIECHIRENZETSU ENDENSENHIFUKUYONANNENSEIJUSHISOSEIBUTSU
JPS53248A (en) * 1976-06-24 1978-01-05 Sumitomo Chem Co Ltd Polyvinyl chloride resin composition
JPS5550046A (en) * 1978-10-04 1980-04-11 Kanegafuchi Chem Ind Co Ltd Vinyl chloride-based resin composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5157751A (en) * 1974-11-16 1976-05-20 Mitsubishi Monsanto Chem HORIECHIRENZETSU ENDENSENHIFUKUYONANNENSEIJUSHISOSEIBUTSU
JPS53248A (en) * 1976-06-24 1978-01-05 Sumitomo Chem Co Ltd Polyvinyl chloride resin composition
JPS5550046A (en) * 1978-10-04 1980-04-11 Kanegafuchi Chem Ind Co Ltd Vinyl chloride-based resin composition

Similar Documents

Publication Publication Date Title
WO1998058019A1 (en) Blends of ethylene-vinyl acetate copolymers and ethylene-vinyl acetate-carbon monoxide terpolymers
JPS62502897A (en) thermoplastic elastomer composition
KR100570260B1 (en) Polyolefin Compositions
US6211291B1 (en) Polyolefin compositions
EP0782590B1 (en) Flexible nonhalogen-containing thermoplastic polyolefin compositions
JP7257805B2 (en) Vinyl chloride resin composition
JPS58217541A (en) Low-temperature impact-resistant resin composition
JPS60155253A (en) Graft copolymer/plastic vonyl polychloride blend as thermoplastic elastomer
US3642948A (en) High impact strength molding mixtures based on chlorinated polyvinylchloride
US3560592A (en) Chlorinated polyvinyl chloride and ethylene/acrylate copolymer compositions
US5250616A (en) High impact polyvinyl halide compositions
JPH07252388A (en) Flame-retardant resin composition
JPH05239269A (en) Flame-retardant resin composition and its production
JP3395309B2 (en) Cold-resistant material
JP2018150488A (en) Vinyl chloride resin composition for pipe and pipe material using the same
JPH10296821A (en) Chlorinated vinyl chloride resin pipe for sprinkler piping
US3600461A (en) Vinyl halide polymeric blends
JP2002275321A (en) Vibration-damping material composition
JPS58219250A (en) Vinyl chloride resin composition
JPS6377943A (en) Ethylene resin molding
JPH07188488A (en) Polyvinyl chloride resin composition
JP2003012886A (en) Hydrogenated dienic polymer composition and molding
JPS62101645A (en) Flame-retardant thermoplastic elastomer composition
JPH0436182B2 (en)
NO176146B (en) Application of a vinyl chloride-containing material to materials where flexibility is required after aging at high temperature