JPS59135247A - Flame-retardant styrene elastomer composition - Google Patents
Flame-retardant styrene elastomer compositionInfo
- Publication number
- JPS59135247A JPS59135247A JP961483A JP961483A JPS59135247A JP S59135247 A JPS59135247 A JP S59135247A JP 961483 A JP961483 A JP 961483A JP 961483 A JP961483 A JP 961483A JP S59135247 A JPS59135247 A JP S59135247A
- Authority
- JP
- Japan
- Prior art keywords
- flame
- styrene elastomer
- copolymer
- retardant styrene
- fluoroelastomer
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はスチレン系エラストマーのり1]燃性絹成物に
関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a styrenic elastomer glue 1] retardant silk composition.
近年、ウレタン系エラストマーで代表されるプラスチッ
クのように加工でき、しかも化学架橋を行わなくどもゴ
ム的な性状を示り熱可塑性エラストマーが注目をあびで
いる。In recent years, thermoplastic elastomers have been attracting attention because they can be processed like plastics, such as urethane elastomers, and yet exhibit rubber-like properties without chemical crosslinking.
特に、最近開発されたスチレン系エラストーマー、づな
わちAがポリスチレンで゛、Bがポリブタジェンあるい
はポリイソプレンに水素を添加して不飽和部をつぶした
ポリマーである八−B−Aブロックコポリマーは、電気
絶縁性が優れ、強じんで、しかも熱軟化温度が160℃
以上と高く、耐熱劣化性も良く、絶縁シート、ヂ」−ブ
、デーゾなどへの今後の発展が期待されているしのであ
る。しかし、このものは、本来易燃性のため、前)ボの
如き優れた特徴を持つにもかかわらず、適用分野が制限
されていた。もし、難燃化できれば多方面にわたる応用
が可能となる。In particular, recently developed styrenic elastomers, ie, 8-B-A block copolymers in which A is polystyrene and B is a polymer obtained by adding hydrogen to polybutadiene or polyisoprene to crush unsaturation, Excellent electrical insulation, strong, and heat softening temperature of 160℃
It has a high resistance to heat deterioration and is expected to be developed into insulating sheets, dielectric sheets, desolation sheets, etc. in the future. However, because this material is inherently flammable, its field of application has been limited, despite having the excellent characteristics described above. If it could be made flame retardant, it could be used in a wide variety of fields.
本発明者らは、この難燃化をはかるために、およそ市場
にてでいる塩素や臭素を含むハロゲン系難燃剤、リン系
難燃剤を系統的に検問を行なった。In order to achieve this flame retardancy, the present inventors systematically investigated halogen-based flame retardants containing chlorine and bromine and phosphorus-based flame retardants available on the market.
その結果、確かに難燃性をもたせることは可能であるが
、反面、分散不良、電気、機械特性の低下表面しみ出し
などの間些か発生しノご。竺に、春;i、いしみ出しに
関して言えば、短時間では大炭夫であ □ってもN”
K 7mの長油に、9たる評価によ□れば、表1しみ出
しの生じないj!!19.燃、剤(、よ見い出されなか
・た。As a result, it is certainly possible to provide flame retardancy, but on the other hand, there are some problems such as poor dispersion, deterioration of electrical and mechanical properties, and surface seepage. In fact, in the spring, when it comes to sewage, in a short period of time it's a big charcoal worker.
According to the evaluation of 9 for K 7m long oil, Table 1 shows no seeping! ! 19. I haven't been able to find any fuel.
この表面しみ出しくJ、難燃性の低下−ψ〕外観不良を
さらに他への悪影響をも□たらり“可能性があり、改1
1
□
善を要づる。This seepage through the surface may lead to a decrease in flame retardancy - ψ], which may cause poor appearance and even have a negative impact on other objects,
1 □ Demand goodness.
ま・lこ、このしみ出しのないものとして、焚11燃性
ポリマー、例えば塩素を含有づるり1][]ブレンゴム
、塩素化ポリ−゛[−ヂレンなどをブレンドすることも
考えられるが、この場合ば耐熱萌化性を但1・さし、□
・。As a material that does not seep out, it is possible to blend flammable polymers such as chlorine-containing Zururi 1] [] Blend rubber, chlorinated poly-[-dylene, etc.]. In some cases, the heat resistant sprouting property should be increased by 1, □
・.
上記スヂーレン系−lラス1〜?一本来の1・0れた耐
熱劣化性が失9れ1.シ、まう□こと(、→、る・本発
明は上記に基いてなされたもので、難燃剤のしみ出しが
なく、しかも耐だ1劣化性に優旧こMli燃性を右する
スヂレン系エラストマー組成物の];を供を目的とづる
ものである。The above-mentioned Sujiren series-l Las 1~? 1. The original 1.0 heat deterioration resistance is lost9. The present invention has been made based on the above, and is a styrene-based elastomer that does not seep out of flame retardant and has excellent deterioration resistance and excellent flame resistance. Composition];
す゛なわち、本発明の組成物は、A −F3−へブロッ
クコポリマー(ただし、Aはポリスチレン、Bはポリブ
タジェンまたはポリイソプレンに水素を、、付加して不
飽和部をつぶしたポリマーである)と含フツ素エラスト
マーをブレンドしたものであって1.このブレンド物に
お〔プる含フツ素エラストマーの含有量が2,0重、1
%以上としたことを特徴とづるものである。In other words, the composition of the present invention comprises an A-F3-block copolymer (where A is polystyrene and B is a polymer obtained by adding hydrogen to polybutadiene or polyisoprene to eliminate unsaturation). It is a blend of fluorine-containing elastomer and has the following characteristics:1. The content of the fluorine-containing elastomer in this blend is 2.0 weight and 1 weight.
% or more.
本発明において臼フッ素エラストマーとしては、従来よ
り公知乃至周知のものなどが、特に限定されることなく
、広範囲にわたって種々例示され1qる。例えば、デ1
−ラフルオロエヂレンーブロビレン系JL重合体、フッ
化ビニリデン−へキナフルオE」プロペン系共重合体、
フッ化ビニリデンータロロ1〜リフルオロ、エチレン系
共重合体、フッ化ビニリデンーペンウノルオ占ブ[1ベ
ン系共重合体、ボリンルΔロアルキノリ含慕アクリレー
ト系エラストマー、ポリフ、ルオロアルキル基含有ポリ
シロキサン系エラストマー、テトラフルオロエヂレンー
ンツ化ビ゛ニリデンーブロビレン糸共重合体、テトラフ
ルAロエチレンー]ニヂレンーイソブヂレン系共車合体
、エチレン〜ヘキザフルAロブロペン系共重合体、テト
ラフルオロ
系共重合体、テトラフルオ[]ゴブレンーエチルビニル
エーテル系共重合体、含フッ素フォスフオニトリル系コ
ーレスト7〜、デトラフル副’ I−I 、U−ヂレン
ーフルオロビニルエーテル系共重合体などが挙げられる
。中でも電気絶縁性を考慮すれば、テトラフルオロエチ
レン−プロピレン系共重合体が好適である。In the present invention, the mill fluoroelastomer is not particularly limited to conventionally known or well-known ones, and a wide variety of fluoroelastomers are exemplified. For example, De1
-Lafluoroedylene-brobylene JL polymer, vinylidene fluoride-hequinafluoride propene copolymer,
Vinylidene fluoride-taloro-1 to fluoro, ethylene-based copolymers, vinylidene fluoride-pen-unol-butyl-[1-ben-based copolymers, borinyl Δroalkynoly-containing acrylate elastomers, polyphenyls, polysiloxanes containing fluoroalkyl groups Elastomer, vinylidene-propylene yarn copolymer containing tetrafluoroethylene, tetrafluoroethylene-]nidylene-isobutylene copolymer, ethylene-hexafluoroethylene-propylene copolymer, tetrafluoroethylene Examples include tetrafluoro[]goblene-ethyl vinyl ether copolymers, fluorine-containing phosphonitrile COLESTO 7~, detrafluor sub' I-I, and U-dylene-fluorovinyl ether copolymers. Among them, a tetrafluoroethylene-propylene copolymer is preferred from the viewpoint of electrical insulation.
含フツ素エラストマーとして好適□なテトラフルオロエ
チレンーブ(」ピレン系共重合体と□しては、主成分の
テトラフルオロエチレンどプロピシンに加え(、これら
ど共重合可能な成分、例えは、エチレン、イソブチレン
、アグリル酸およびそのアルキルニスデル、メタクリル
酸dゴよびぞのアルキルニスデル、フッ化ビニル、フッ
化ビニリデン、ヘキリ′フルAロプロペン、クロロエチ
ルビニルエーテル、り11 II l−リフル1−ロエ
チレン、パーフルオロアルキルビニルエーテル等を適当
に含有せしめたものであってもよい。かがる共重合体に
おい−c1デトラフルオロエチレン/プロピレンの含有
モル比どしては9515〜30/70、特に90/10
〜/l 5 / 55の範囲から選定゛づることが、耐
熱性、成形性等の面から好ましく、また、適宜加えられ
る主成分以外の成分の含有量としては通常50モル%以
下、特に30モル%以下の範囲から選定覆ることが好ま
しい。Tetrafluoroethylene copolymers suitable as fluorine-containing elastomers are pyrene-based copolymers. , isobutylene, agrilic acid and its alkylnisdales, methacrylic acid and its alkylnisdales, vinyl fluoride, vinylidene fluoride, hexyl-fluor-A lopropene, chloroethyl vinyl ether, 11 II l-lyfur-1-loethylene, It may also contain a suitable amount of perfluoroalkyl vinyl ether, etc. In the dark copolymer, the molar ratio of -c1 detrafluoroethylene/propylene contained is 9515 to 30/70, especially 90/70. 10
It is preferable to select from the range of ~/l 5/55 from the viewpoint of heat resistance, moldability, etc. Also, the content of components other than the main component that may be added as appropriate is usually 50 mol% or less, particularly 30 mol %. It is preferable to select from a range of % or less.
含フッ素エラス1−マーのブレンド量は、組成物仝吊の
20重小事以上と覆る必要があり、20重ω%未)^I
Cは所望の難燃性を(=J与できなべなる。The blending amount of the fluorine-containing elastomer 1-mer must cover at least 20 major factors that affect the composition, and must be less than 20 major ω%)^I
C can provide the desired flame retardancy (=J).
本発明においては、必要に応じてガ燃助剤のイ11川も
可能□であり、例えば三酸化アンチモン、ボウrA l
li鉛、酸化ジルコニウムなどがあげられる。In the present invention, it is also possible to use fuel auxiliaries as needed, such as antimony trioxide, aluminum
Examples include li lead and zirconium oxide.
これ以外に、しみ出しの生じない範囲で他の鮨燃剤、例
えばパークロロシクロペンタデカン、デカjロモジフ1
ニルニーデルなどを併用しても良く、また、通常のゴ仏
に用いら□れるケイ酸アルミニウム、クイ酸マグネシウ
ム、炭酸カルシウムなどの充填剤、酸化防仕剤、滑剤、
安定剤を加えても差し皮膚ない。勿論、特性低下をIB
がない範囲でのポリエチレンなど、伯のポリマーの添加
も可能である。In addition to this, other sushi fuels such as perchlorocyclopentadecane, decaj lomodif 1 may be used within the range that does not cause seepage.
It may also be used in combination with Nilneedel, fillers such as aluminum silicate, magnesium citrate, calcium carbonate, etc., which are used in ordinary gobutsu, oxidation inhibitors, lubricants,
Even if a stabilizer is added, there will be no damage to the skin. Of course, IB
It is also possible to add other polymers, such as polyethylene, to the extent that they are free.
JメJ:、、本発明の実施例を比較例と対比して説明づ
る。。J.J.: Examples of the present invention will be explained in comparison with comparative examples. .
第1表に示づ′配合成分を所定量180℃以十ぐMA練
混合後、180 ”C15分の条件で厚さ2 mmのシ
ー1〜にプレス成形した。The ingredients shown in Table 1 were mixed in predetermined amounts at 180 DEG C. by MA kneading, and then press-molded into sheets 1 to 2 mm thick under conditions of 180"C for 15 minutes.
かくしで得られたシートの8梗特性についての、I″P
価結果を第1表の下欄に示′T+ +1なJ5、特性の
評価は下記による。I″P regarding the 8-point characteristics of the sheet obtained by hiding
The evaluation results are shown in the lower column of Table 1.
勤燃性: J l5C−3005に準拠3、しみ出しニ
ジ−(へを120’CX120時間と常温×12時聞0
ヒー1〜1ノイクルをか(」ながら8力月放函しCi?
lt価した。Flammability: Compliant with J15C-3005 3, oozing temperature (120'C x 120 hours and room temperature x 12 hours 0
He did 1~1 Noikuru ('' while releasing 8 Rikizuki and Ci?
It was worth it.
耐熱劣化性:シートを160°CX 101.’l熱劣
化した後に折り曲げ、クラックの発生の
有無を評価した。Heat deterioration resistance: sheet heated to 160°C 101. After thermal deterioration, it was bent and the presence or absence of cracks was evaluated.
第 1 表
ムー二粘曵M++alOO℃:ε30
(2)アク[]シン604 (商品名)(3) j、l
A索rr=10%、ムー二粘度MS+ 十a ’I00
”C:80以上、実施例J’Li J、:び比較例から
も明らかなように、本発明によれば離燃性に優れると共
に難燃剤のしみ出しがなく、しかも耐熱劣化性に優れた
スブレン系]−ラス1〜マー組成物が41Jられること
になる。。Table 1 Mouni viscosity M++ alOO℃: ε30 (2) Aku [] Shin 604 (trade name) (3) j, l
A rope rr=10%, Mouni viscosity MS+ 10a'I00
"C: 80 or more, Example J'Li J: As is clear from the comparative examples, the present invention has excellent flame retardant properties, no exudation of flame retardant, and excellent heat deterioration resistance. 41 J of the soubrene-based]-Las 1-mer composition will be used.
33
Claims (1)
リスチレン、Bはポリブタジェンまlこ(よ/I<リイ
ソプレンに水素を付加して不飽和部をつ・S−したポリ
マーである)法ゝ含フッ素エラストマーをブレンドした
ものであって、このブレンド物における含フツ素エラス
トマーの含有量が20重搭%以上であることを特徴とす
る到1燃性メチレン系エラス1ヘマー組成物。 2 含フツ素エラストマーがテトラフルA1コ■チレン
ーブ[1ピレン系共重合体であることを特徴とする特許
請求の範囲第1項記載の難燃性スチレン系エラスト−組
成物。[Scope of Claims] 1 A-B-A block copolymer (where △ is polystyrene and B is polybutadiene (Y/I< a polymer made by adding hydrogen to isoprene to create an unsaturated moiety) A highly flammable methylene-based elastomer composition, which is a blend of a fluorine-containing elastomer and characterized in that the content of the fluorine-containing elastomer in the blend is 20% by weight or more. 2. The flame-retardant styrenic elastomer composition according to claim 1, wherein the fluorine-containing elastomer is a tetraful A1 co-styrene copolymer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP961483A JPS59135247A (en) | 1983-01-24 | 1983-01-24 | Flame-retardant styrene elastomer composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP961483A JPS59135247A (en) | 1983-01-24 | 1983-01-24 | Flame-retardant styrene elastomer composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59135247A true JPS59135247A (en) | 1984-08-03 |
JPS6367819B2 JPS6367819B2 (en) | 1988-12-27 |
Family
ID=11725166
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP961483A Granted JPS59135247A (en) | 1983-01-24 | 1983-01-24 | Flame-retardant styrene elastomer composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59135247A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104262736A (en) * | 2014-11-03 | 2015-01-07 | 苏州钧隆塑胶有限公司 | High-elasticity plastic |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5182343A (en) * | 1974-12-06 | 1976-07-19 | Gen Electric |
-
1983
- 1983-01-24 JP JP961483A patent/JPS59135247A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5182343A (en) * | 1974-12-06 | 1976-07-19 | Gen Electric |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104262736A (en) * | 2014-11-03 | 2015-01-07 | 苏州钧隆塑胶有限公司 | High-elasticity plastic |
Also Published As
Publication number | Publication date |
---|---|
JPS6367819B2 (en) | 1988-12-27 |
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