JPH03223352A - Flame-retardant resin composition - Google Patents

Flame-retardant resin composition

Info

Publication number
JPH03223352A
JPH03223352A JP2020029A JP2002990A JPH03223352A JP H03223352 A JPH03223352 A JP H03223352A JP 2020029 A JP2020029 A JP 2020029A JP 2002990 A JP2002990 A JP 2002990A JP H03223352 A JPH03223352 A JP H03223352A
Authority
JP
Japan
Prior art keywords
flame
resin composition
elastomer
polyolefin polymer
silicone
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
JP2020029A
Other languages
Japanese (ja)
Other versions
JP2818240B2 (en
Inventor
Toshihiro Arai
敏弘 新井
Hideo Sunatsuka
砂塚 英夫
Michio Matsuura
松浦 三千男
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.)
Fujikura Ltd
Original Assignee
Fujikura 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 Fujikura Ltd filed Critical Fujikura Ltd
Priority to JP2020029A priority Critical patent/JP2818240B2/en
Publication of JPH03223352A publication Critical patent/JPH03223352A/en
Application granted granted Critical
Publication of JP2818240B2 publication Critical patent/JP2818240B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Organic Insulating Materials (AREA)
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Abstract

PURPOSE:To impart a sufficient flame retardance and good mechanical and low-temp. properties to a polyolefin polymer by compounding the polymer with a thermoplastic 1,2-polybutadiene elastomer and a silicone resin. CONSTITUTION:100 pts.wt. polyolefin polymer is compounded with 0.1-100 pts.wt. thermoplastic 1,2-polybutadiene elastomer and 0.5-30 pts.wt. silicone resin. As the elastomer, a syndiotactic, lowly crystalline thermoplastic elastomer having a 1,2-bond content of 90% or higher, a mol.wt. of 100000 to several hundred thousands, and a degree of crystallization of 15-35% is used. Examples of the silicone are dimethylpolysiloxane, dimethyldiphenylpolysiloxane, amino-modified silicone, and epoxy-modified silicone.

Description

【発明の詳細な説明】 卒業上の利用分野 この発明は、電線、ケーブル等の被覆材料、接続材料な
とに用いられるポリオレフィン系ポリマーを主体とした
難燃性樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Application This invention relates to a flame-retardant resin composition mainly containing a polyolefin polymer, which is used as a coating material for electric wires, cables, etc., and as a connecting material.

「従来の技術」 ポリオレフィン系ポリマーを難燃化するための難燃化技
術の1つに、ポリエチレン、ポリプロピレンなとのポリ
オレフィン系ポリマーに対して水酸化アルミニウム、水
酸化マグネシウムなどの含水無機充填剤を配合するもの
か知られている。
"Conventional technology" One flame retardant technology for making polyolefin polymers flame retardant is to add hydrous inorganic fillers such as aluminum hydroxide and magnesium hydroxide to polyolefin polymers such as polyethylene and polypropylene. It is known whether it is compounded.

この含水無機充填剤を配合するものにあっては、燃焼時
に有害なハロケン含有カスか発生しない利点はあるもの
の十分な難燃性を得るためには、含水無機充填剤を多量
に添加する必要かあり、多量の添加では引張特性なとの
機械的特性や耐寒性の悪化を招く不都合かある。
Products containing this hydrous inorganic filler have the advantage of not generating harmful halogen-containing scum during combustion, but in order to obtain sufficient flame retardancy, it is necessary to add a large amount of the hydrous inorganic filler. However, adding a large amount may lead to deterioration of mechanical properties such as tensile properties and cold resistance.

[発明が解決しようとする課題。[Problem that the invention seeks to solve.

よって、この発明における課題は、十分な難燃性を有し
、かつその機械的特性、耐寒性か良好なポリオレフィン
系ポリマーを主体とする難燃性樹脂組成物を提供するこ
とにある。
Therefore, an object of the present invention is to provide a flame-retardant resin composition mainly composed of a polyolefin polymer that has sufficient flame retardancy and has good mechanical properties and cold resistance.

[課題を解決するための手段f この発明では、ポリオレフィン系ポリマー100重量部
に対して1.2−ポリブタジエン系熱可塑性エラストマ
ー0.1〜10 o重量g、シ’) コーン樹脂0.5
 〜30重量部を配合することによって、上記課題を解
決するようにした。
[Means for Solving the Problems f] In this invention, 1.2-polybutadiene thermoplastic elastomer 0.1 to 10 g, Si') cone resin 0.5 to 100 parts by weight of polyolefin polymer.
By blending ~30 parts by weight, the above problem was solved.

以下、この発明の詳細な説明する。The present invention will be described in detail below.

この発明におけるポリオレフィン系ポリマーとしては、
高密度ポリエチレン(HDPE)、低密度ポリエチレン
(LDPE)、直鎖状低密度ポリエチレン(LLDPE
)なとのポリエチレン、ポリプロピレン、ポリブテン−
11ポリ4−メチルペンテン−1なとのα−オレフィン
ホモポリマーエチレン−エチルアクリレート共重合体(
EEA)、エチレン−酢酸ビニル共重合体(EVA) 
、エチレン−アクリル酸共重合体(EAA)、エチレン
プロピレン共重合体、エチレン−ブテン−1共重合体、
エチレン−プロピレンニジエン共重合体なとのエチレン
と他のモノマーとの共重合体なとの単独もしくは複数の
ポリマーのブレンド物等が用いられる。
As the polyolefin polymer in this invention,
High density polyethylene (HDPE), low density polyethylene (LDPE), linear low density polyethylene (LLDPE)
) Polyethylene, polypropylene, polybutene
11 α-olefin homopolymer ethylene-ethyl acrylate copolymer with poly4-methylpentene-1 (
EEA), ethylene-vinyl acetate copolymer (EVA)
, ethylene-acrylic acid copolymer (EAA), ethylene-propylene copolymer, ethylene-butene-1 copolymer,
Single or blends of a plurality of polymers such as ethylene-propylene diene copolymer and copolymers of ethylene and other monomers are used.

また、この発明で使用される1、2−ポリブタジエン系
熱可塑性エラストマーとしては、1.2結合が90%以
上で、分子量がlO万〜数10万、結晶化度が15〜3
5%のンンジオクタチノク構造を有する低結晶性の熱可
塑性エラストマーか用いられ、伸びが300%以上のゴ
ム的性質を有するものが用いられる。このエラストマー
の具体的なものとしては、rJsRRB805j、r 
JSRRB81O」  、 rJSRRBg20j  
、 rJsRRB83J  、 r JSRRB840
j  (商品名、日本合成ゴム製)なとかある。
In addition, the 1,2-polybutadiene thermoplastic elastomer used in this invention has a 1.2 bond of 90% or more, a molecular weight of 10,000 to several 100,000, and a crystallinity of 15 to 3.
A low-crystalline thermoplastic elastomer having a polygonal structure of 5% is used, and one having rubber-like properties with an elongation of 300% or more is used. Specific examples of this elastomer include rJsRRB805j, r
JSRRB81O”, rJSRRBg20j
, rJsRRB83J, rJSRRB840
J (product name, made by Japan Synthetic Rubber).

このエラストマーは上述のポリオレフィン系ポリマーと
相溶性が良好てあり、均一な組成物を形成する。
This elastomer has good compatibility with the above-mentioned polyolefin polymer and forms a uniform composition.

この1.2−ポリブタジエン系熱可塑性エラストマーの
配合量はポリオレフィン系ポリマー100重量部に対し
て0.1〜100重量部とされる。
The blending amount of the 1,2-polybutadiene thermoplastic elastomer is 0.1 to 100 parts by weight per 100 parts by weight of the polyolefin polymer.

0.1重量部未満では難燃性の改善か見られず、100
重量部を越えるとベースのポリオレフィン系ポリマーの
特性を損うことになる。
If it is less than 0.1 part by weight, no improvement in flame retardancy can be seen;
If it exceeds the weight part, the properties of the base polyolefin polymer will be impaired.

また、この発明で使用されるシリコーン樹脂としては、
ジメチルポリシロキサン、ジメチルジフェニルポワシロ
キサン、アミン変性シリコーン、メルカプト変性シリコ
ーン、エポキシ変性シリコーンなどの原則として一3i
−0−骨格を有し、側鎖および末端基にはハロゲンを含
まない官能基を有するものが挙げられる。官能基として
は、ビニル基、アミノプロピル基、グリシドキシプロピ
ル基なとの文応性基、メチル基、エチル基、プロピル基
本、フェニル基、アシル基、水素原子なとがある。その
分子量は数百ないし数百刃の範囲であり、その形態はオ
イル状、ワニス状、樹脂状なとのいかなるものであって
もよい。
In addition, the silicone resin used in this invention includes:
In principle, 13i such as dimethylpolysiloxane, dimethyldiphenylpoisoxane, amine-modified silicone, mercapto-modified silicone, epoxy-modified silicone, etc.
Examples include those having a -0- skeleton and a functional group that does not contain halogen in the side chain or terminal group. Examples of the functional group include a vinyl group, an aminopropyl group, a glycidoxypropyl group, a methyl group, an ethyl group, a propyl group, a phenyl group, an acyl group, and a hydrogen atom. Its molecular weight ranges from several hundred to several hundred blades, and its form may be oil-like, varnish-like, or resin-like.

このシリコーン樹脂の配合量は、ポリオレフィン系ポリ
マー100重量部に対して0.5〜30小量部の範囲と
される。0.5 重量部未満では難燃性改善効果か得ら
れず、30重量部を超えると組成物の機械的特性か低下
して不都合となる。
The amount of the silicone resin blended is in the range of 0.5 to 30 parts by weight per 100 parts by weight of the polyolefin polymer. If it is less than 0.5 parts by weight, no flame retardant improvement effect can be obtained, and if it exceeds 30 parts by weight, the mechanical properties of the composition will deteriorate, resulting in disadvantages.

この発明の難燃性組成物では、上記1.2−ポノフタン
エン系熱可塑性エラストマーとシリコーン樹脂との併用
により、相乗的な難燃性改善効果が得られる。
In the flame retardant composition of the present invention, a synergistic flame retardant improvement effect can be obtained by using the 1,2-ponophthanene thermoplastic elastomer and the silicone resin together.

また、この発明の難燃性樹脂組成物では、さらに他の難
燃剤を添加することができ−る。このような難燃剤とし
ては、水酸化アルミニウム、水酸化マグ不ソウム、赤リ
ン、カーボンフ゛ラックなとが挙げられる。
Further, in the flame retardant resin composition of the present invention, other flame retardants can be further added. Examples of such flame retardants include aluminum hydroxide, magnesium hydroxide, red phosphorus, and carbon fiber.

さらに、この難燃性樹脂組成物には、必要に応じて無機
難燃剤、軟化剤、着色剤、老化防止剤、安定剤なとを適
宜添加することかできる。
Furthermore, an inorganic flame retardant, a softener, a coloring agent, an anti-aging agent, a stabilizer, etc. can be added to this flame-retardant resin composition as necessary.

このような難燃性樹脂組成物にあっては、l。In such a flame retardant resin composition, l.

2−ポリブタジエン系熱可塑性エラストマーとシリコー
ン樹脂との併用により良好な難燃性か得られるとともに
引張特性なとの機械的特性や耐寒性などの温度特性の低
下かなく、優れた物性を有するものとなる。
By using a 2-polybutadiene thermoplastic elastomer in combination with a silicone resin, good flame retardancy can be obtained, and it has excellent physical properties without deterioration of mechanical properties such as tensile properties or temperature properties such as cold resistance. Become.

また、1.2−ポリブタジエン系熱可塑性エラストマー
はポリオレフィン系ポリマーとの相溶性が良好であるの
で、これか成形物表面に滲出することがない。
Furthermore, since the 1,2-polybutadiene thermoplastic elastomer has good compatibility with the polyolefin polymer, it does not ooze out onto the surface of the molded product.

以下、具体例を示して作用、効果を明細にする。Hereinafter, specific examples will be shown and the functions and effects will be explained in detail.

「実施例」 第1表に示す配合組成の樹脂組成物を調製し、押出成形
してシート状の試片を得た。
"Example" A resin composition having the composition shown in Table 1 was prepared and extruded to obtain a sheet-like specimen.

この試片について、酸素指数、引張強度、伸び、脆化温
度(耐寒性)を測定した。
The oxygen index, tensile strength, elongation, and embrittlement temperature (cold resistance) were measured for this specimen.

結果を第1表に併せて示した。The results are also shown in Table 1.

第1表から明らかなように、この発明の難燃性樹脂組成
物は、良好な難燃性と機械的特性および温度特性を有し
ていることがわかる。
As is clear from Table 1, the flame-retardant resin composition of the present invention has good flame retardancy, mechanical properties, and temperature properties.

−発明の効果≦ 以上説明したように、この発明の難燃性樹脂組成物はポ
リオレフィン系ポリマー100重量部に対して1,2−
ポリブタンエン系熱可塑性エラストマーo、t−too
重量部、シリコーン樹脂05〜30 ’14 m部を配
合したものであるので、優れた難燃性を有するとともに
機械的特性や耐寒性か良好なしのとなる。
-Effects of the Invention≦ As explained above, the flame-retardant resin composition of the present invention has 1,2-
Polybutanene thermoplastic elastomer o, t-too
Since it contains 05-30'14 m parts of silicone resin by weight, it has excellent flame retardancy and excellent mechanical properties and cold resistance.

Claims (1)

【特許請求の範囲】[Claims]  ポリオレフィン系ポリマー100重量部に対し、1,
2−ポリブタジエン系熱可塑性エラストマー0.1〜1
00重量部、シリコーン樹脂0.5〜30重量部を配合
したことを特徴とする難燃性樹脂組成物。
1, per 100 parts by weight of polyolefin polymer
2-Polybutadiene thermoplastic elastomer 0.1-1
A flame-retardant resin composition characterized in that it contains 0.00 parts by weight and 0.5 to 30 parts by weight of a silicone resin.
JP2020029A 1990-01-30 1990-01-30 Flame retardant resin composition Expired - Lifetime JP2818240B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2020029A JP2818240B2 (en) 1990-01-30 1990-01-30 Flame retardant resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2020029A JP2818240B2 (en) 1990-01-30 1990-01-30 Flame retardant resin composition

Publications (2)

Publication Number Publication Date
JPH03223352A true JPH03223352A (en) 1991-10-02
JP2818240B2 JP2818240B2 (en) 1998-10-30

Family

ID=12015647

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2020029A Expired - Lifetime JP2818240B2 (en) 1990-01-30 1990-01-30 Flame retardant resin composition

Country Status (1)

Country Link
JP (1) JP2818240B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6569931B2 (en) * 2000-06-12 2003-05-27 Dow Corning Corporation Thermoplastic elastomer composition, method of preparation, and molded products thereof
CN104311917A (en) * 2014-10-30 2015-01-28 安徽电信器材贸易工业有限责任公司 Impact-resistant anti-aging cable material and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6569931B2 (en) * 2000-06-12 2003-05-27 Dow Corning Corporation Thermoplastic elastomer composition, method of preparation, and molded products thereof
CN104311917A (en) * 2014-10-30 2015-01-28 安徽电信器材贸易工业有限责任公司 Impact-resistant anti-aging cable material and preparation method thereof

Also Published As

Publication number Publication date
JP2818240B2 (en) 1998-10-30

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