JPS62167339A - Flame-retardant resin composition - Google Patents

Flame-retardant resin composition

Info

Publication number
JPS62167339A
JPS62167339A JP797486A JP797486A JPS62167339A JP S62167339 A JPS62167339 A JP S62167339A JP 797486 A JP797486 A JP 797486A JP 797486 A JP797486 A JP 797486A JP S62167339 A JPS62167339 A JP S62167339A
Authority
JP
Japan
Prior art keywords
olefin
flame
magnesium hydroxide
resin composition
groups
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
JP797486A
Other languages
Japanese (ja)
Inventor
Kazuo Hoshi
和雄 星
Yoshio Nakagawa
中川 凱夫
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite 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 Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP797486A priority Critical patent/JPS62167339A/en
Publication of JPS62167339A publication Critical patent/JPS62167339A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:The titled composition preventing drip in combustion, causing neither halogenous corrosive properties nor poisonous gas, having improved processing properties, obtained by blending an '-olefin (co)polymer having specific gravity with a specific amount of magnesium hydroxide subjected to surface treatment. CONSTITUTION:100pts.wt. alpha-olefin (co)polymer (e.g., polyethylene, crystalline propylene-ethylene block copolymer, etc.,) having <=0.92 gravity is blended with 50-250pts.wt. magnesium hydroxide subjected to surface treatment with one or more of a silane coupling agent, a silicone derivative or a fatty acid (metallic salt).

Description

【発明の詳細な説明】 (産業上の利用分野〕 本発明は、難燃性に優れ、燃焼時にあけるドリップ防止
およびノンハロゲン系の腐蝕性、有害性ガスの発生せず
、機械物性のバランスのとれ、更には押出加工性に優れ
た密度が0.92以下のα−オレフィンの単独重合体又
はその共重合体を使用したオレフィン系離燃性樹脂組成
物に関するものである。
Detailed Description of the Invention (Field of Industrial Application) The present invention has excellent flame retardancy, prevents dripping during combustion, is non-halogen-based, corrosive, does not generate harmful gases, and has well-balanced mechanical properties. Furthermore, the present invention relates to an olefin-based flame retardant resin composition using an α-olefin homopolymer or copolymer thereof having a density of 0.92 or less and having excellent extrusion processability.

〔従来技術〕[Prior art]

従来、電線、ケーブルをはじめ電器製品の絶縁材料とし
て多用されているポリオレフィン組成物に難燃性を付与
するためには、ポリオレフィンにハロゲン化合物と三酸
化アンチモンを添加することにより達成されていた。し
かるにこれらの組成物はハロゲン化合物であり燃焼時に
ハロゲン化ガスを発生するので人体に有害でおり、かつ
全屈が腐蝕されるので好ましくなかった。
Conventionally, flame retardancy has been achieved in polyolefin compositions, which are often used as insulating materials for electric wires, cables, and other electrical appliances, by adding halogen compounds and antimony trioxide to polyolefins. However, these compositions are halogenated compounds and emit halogenated gas when burned, which is harmful to the human body and corrodes the entire bend, which is not desirable.

一方、従来の難燃性組成物におっては、難燃性は水和金
属化合物でノンハロゲン化を達成しているものの、ベー
スになる樹脂については、特許第1231199 @に
みられるように結晶状オレフィン単合体樹脂の他に、ポ
リスチレン、ABS、ナイロン等の熱可塑性樹脂をあげ
ているものが多くこれら樹脂の燃焼した場合のスチレン
系、アミド系が発生するノンハロゲンではあるが相当量
の有害ガスを発生する片手落らのところがみられた。
On the other hand, in conventional flame retardant compositions, flame retardancy is achieved by non-halogenated hydrated metal compounds, but the base resin is crystalline as seen in Patent No. 1231199 @. In addition to olefin monopolymer resins, there are many that list thermoplastic resins such as polystyrene, ABS, and nylon, and when these resins are burned, they generate styrene and amide resins, which are non-halogen, but emit a considerable amount of harmful gas. The area where one hand fell off was seen.

また更に上記特許第1231199号にみられるように
熱可塑性樹脂、水酸化マグネシウムおよび炭素粉末の三
者による難燃向上を主体とした、自消性樹脂組成物は用
途によっては、特に通信線の絶縁線およびジャケットな
どは、多色、例えば8色などのカラー表示を限定されて
おり、炭素粉末によって難燃性向上を目的とした組成物
は、全く実際にそぐわない組成物があった。
Furthermore, as seen in the above-mentioned Patent No. 1231199, self-extinguishing resin compositions mainly consisting of thermoplastic resin, magnesium hydroxide, and carbon powder to improve flame retardancy can be used for some applications, especially for insulation of communication lines. Lines, jackets, and the like are limited to multiple colors, for example, eight colors, and some compositions that aim to improve flame retardancy using carbon powder are completely unsuitable for actual use.

〔発明の目的〕[Purpose of the invention]

本発明は、前記の事情を考慮して成されたもので、その
目的とするところは、火災発生時の人体への安全性を高
く周囲の金属等を腐蝕させることもない、ノンハロゲン
ガスも元より有害ガスを全く発生しない、クリーンな無
公害化を達成したものである。
The present invention has been made in consideration of the above circumstances, and its purpose is to provide a gas that is highly safe to the human body in the event of a fire, does not corrode surrounding metals, and is a non-halogen gas. It is a clean and non-polluting system that does not emit any harmful gases.

即ち、本発明は、ポリスチレン、ABS、ナイロン等の
有害ガスを発生する樹脂を対象外として、α−オレフィ
ン単独重合体およびα−オレフィンの共重合体を使用し
、しかもカーボンブラック等の炭素粉末を使用すること
を目的とせず、用途に応じて自由自在にカラーリングが
可能であり、さらには樹脂密度を0.92以下の低結晶
性の柔軟なものを使用し、1種以上のシランカップリン
グ剤などで表面処理された水酸化マグネシウムを使用す
ることにより、多量の水和金属を充填しても、非常に柔
軟で低温特性、および加工性に優れ、従来の炭素粉末の
添加での難燃性効果以上の多量の水和金属化合物を充填
できる難燃樹脂組成物を提供することにある。
That is, the present invention excludes resins that generate harmful gases such as polystyrene, ABS, and nylon, and uses α-olefin homopolymers and α-olefin copolymers, and carbon powder such as carbon black. It is not intended for use, and can be freely colored according to the purpose, and furthermore, it uses a low-crystalline flexible material with a resin density of 0.92 or less, and one or more types of silane coupling. By using magnesium hydroxide that has been surface-treated with a chemical agent, it has excellent flexibility, low-temperature properties, and processability even when filled with a large amount of hydrated metal, and is flame retardant compared to the conventional addition of carbon powder. The object of the present invention is to provide a flame-retardant resin composition that can be filled with a large amount of a hydrated metal compound that has a superior performance effect.

〔発明の構成〕[Structure of the invention]

本発明の難燃性樹脂組成物は、いずれもハロゲン元素を
一切含まず、燃焼しても有害性ガスを全く発生せず、樹
脂組成物の自由に着色化が容易であることを特徴とする
ものでおる。
The flame-retardant resin compositions of the present invention are characterized in that they do not contain any halogen elements, do not generate any harmful gases even when burned, and are easy to freely color the resin composition. It's something.

(1)本発明において用いられるα−オレフィンの単独
重合体又は共重合体は、エチレン、プロピレン等のα−
オレフィンの単独重合体又は、α−オレフィンと他のα
−オレフィンとの結晶性のブロック又はランダム共重合
体例えば、結晶性プロピレン−エチレンブロック共重合
体、エチレン−ブテン−1ランダム共重合体、プロピレ
ン−ブテン−1ランダム共重合体、又は、α−オレフィ
ンを主体とする、酢酸ビニル、無水マレイン酸、アクリ
ル酸等の極性モノマーとの共重合体(グラフト共重合体
を含む)およびこれらの混合物であり、その比重が0.
92以下のものである。
(1) The α-olefin homopolymer or copolymer used in the present invention is an α-olefin such as ethylene or propylene.
Homopolymers of olefins or α-olefins and other α-olefins
- crystalline block or random copolymers with olefins, such as crystalline propylene-ethylene block copolymers, ethylene-butene-1 random copolymers, propylene-butene-1 random copolymers, or α-olefins; copolymers (including graft copolymers) with polar monomers such as vinyl acetate, maleic anhydride, and acrylic acid, and mixtures thereof, whose specific gravity is 0.
92 or less.

これら混合物の組み合わせは樹脂組成物の表面硬度、耐
寒性、耐ストレスクラッキング、接着性向上などの諸々
の要求により組み合わせが可能であり、いずれの組み合
わせも容易に混練溶融される。
Combinations of these mixtures can be made depending on various requirements such as improving the surface hardness, cold resistance, stress cracking resistance, and adhesion of the resin composition, and any combination can be easily kneaded and melted.

(2)本発明において使用される水酸化マグネシウムは
、シランカップリング剤シリコーン誘導体又は脂肪酸、
脂肪酸金属塩で表面処理を施したものを用いる。
(2) Magnesium hydroxide used in the present invention is a silane coupling agent silicone derivative or a fatty acid,
Use one that has been surface-treated with a fatty acid metal salt.

(i)シランカップリング剤としては分子内の一方の末
端に無機質と反応する反応基(メトキシ基、エトキシ基
、カルボキシル基、セロソルブ基など)でおり、これは
一般的に三官能基を有する場合が多いが、三官能、−官
能を有する場合でももちろんよい。またもう一方の末端
には、有機材料である樹脂側と化学結合する反応基(ビ
ニル基、エポキシ基、メタクリル基、アミノ基、メルカ
プト基など)を有するもので主鎖がフルコキシオリゴマ
ーを骨格とするものである。
(i) A silane coupling agent has a reactive group (methoxy group, ethoxy group, carboxyl group, cellosolve group, etc.) that reacts with an inorganic substance at one end of the molecule, and this generally has a trifunctional group. However, it is of course also possible to have trifunctional or -functional functional groups. In addition, the other end has a reactive group (vinyl group, epoxy group, methacrylic group, amino group, mercapto group, etc.) that chemically bonds with the resin side of the organic material, and the main chain has a flukoxy oligomer skeleton. It is something to do.

(11)シリコーン誘導体としては、ジメチルポリシロ
キサンのメチル基の一部を各種の有機基を置換したタイ
プで、各種の変性有機基としては、α−メチルスチレン
基、α−オレフィン基、ポリエーテル基、アルコール基
、フルオロアルキル基なとの相溶性、親水性、潤滑性、
祁水性などを改良することを目的とする変性基、アミン
基メルカプル基、エポキシ基、カルボキシル基などの反
応性、吸着性を目的とした変成基、高級脂肪酸、カルバ
ナ、アミドを置換した離型、つや出しを目的とした変成
基、メタアクリロキシプロピル基を有する反応性に富ん
だ変成型、末端にOH基、NH2基を有する反応型など
、多種多様の変成基を置換して導入したシリコーン変成
誘導体があげられる。
(11) The silicone derivative is a type in which a part of the methyl group of dimethylpolysiloxane is substituted with various organic groups, and the various modified organic groups include α-methylstyrene group, α-olefin group, and polyether group. , compatibility with alcohol groups, fluoroalkyl groups, hydrophilicity, lubricity,
Modified groups for the purpose of improving water repellency, etc., modified groups for the purpose of reactivity and adsorption such as amine groups, mercapuru groups, epoxy groups, carboxyl groups, mold release substituted with higher fatty acids, carbana, and amide; Silicone modified derivatives introduced by substitution with a wide variety of modified groups, including modified groups for the purpose of polishing, highly reactive modified types with methacryloxypropyl groups, and reactive types with OH groups and NH2 groups at the terminals. can be given.

(iii)脂肪酸としては飽和および不飽和脂肪酸があ
り、炭素数が6以上22までの脂肪酸を指すが特に01
8のステアリン酸、オレイン酸があげられる。
(iii) Fatty acids include saturated and unsaturated fatty acids, and refers to fatty acids with carbon numbers of 6 to 22, especially 01
Examples include stearic acid and oleic acid.

(iV)脂肪酸金属塩としては、上記の脂肪酸が金属と
結合した金属石けんを示し、特にステアリン酸ソーダ、
オレイン酸カリ、などがあげられる。
(iv) Fatty acid metal salts include metal soaps in which the above-mentioned fatty acids are bonded to metals, particularly sodium stearate,
Examples include potassium oleate.

もちろん脂肪酸としては直鎖飽和型、不飽和型を問わず
側鎖部分が金属と結合したものも、もちろん有効である
Of course, fatty acids with a side chain bonded to a metal are also effective, regardless of whether they are linear saturated or unsaturated.

上記(i)〜(iV)によって又はその混合体によって
表面処理された水酸化マグネシウムを50重優品から2
50重1部で連用した場合、低密度の低結晶性ポリマー
と相溶するか又は反応し高充填した場合でも容易に、低
温特性、柔軟性および加工性の優れた難燃組成物を形成
できるものであるが、50重量部以下ではその難燃効果
は著しく低下してしまう。また250重量部以上では、
難燃性が著しく向上するものの、柔軟性、低温特性等の
機械特性が低下し、加工性が極端に悪くなることを確認
している。
Magnesium hydroxide surface-treated by the above (i) to (iV) or a mixture thereof, from 50 to 2
When used continuously at 50 parts by weight, it is compatible with or reacts with low-density, low-crystalline polymers, and can easily form flame-retardant compositions with excellent low-temperature properties, flexibility, and processability even when highly loaded. However, if the amount is less than 50 parts by weight, the flame retardant effect will be significantly reduced. In addition, at 250 parts by weight or more,
It has been confirmed that although flame retardancy is significantly improved, mechanical properties such as flexibility and low-temperature properties are reduced, and workability is extremely poor.

(3)他の添加物 本発明の難燃樹脂組成物は所望により、酸化防止剤、中
和剤、紫外線吸収剤、帯電防止剤、顔料、分散剤、滑剤
、増粘剤等の通常配合されるものは配合することができ
る。
(3) Other additives The flame retardant resin composition of the present invention may contain antioxidants, neutralizers, ultraviolet absorbers, antistatic agents, pigments, dispersants, lubricants, thickeners, etc., if desired. can be blended.

(4)表面処理方法 処理方法は、ヘンシェルミキサー、ブレダー等の攪拌機
械で充分であり、機種によっては、処理の攪拌時間の長
短の差はあるものの、特別の装置を必要としない。
(4) Surface treatment method A stirring machine such as a Henschel mixer or a blender is sufficient for the treatment method, and no special equipment is required, although the length of stirring time for treatment may vary depending on the model.

添加の方法は、滴下式、一括投入方式など、処理剤の使
用方法について使い分ける必要がある。
It is necessary to use a different method of addition depending on how the processing agent is used, such as a dripping method or a bulk addition method.

また処理剤の性質によっては水又はアルコール溶剤など
で希釈して用いてもよい。
Further, depending on the properties of the processing agent, it may be used after being diluted with water or an alcohol solvent.

また、水酸化マグネシウムの生産ライン工程での処理も
できる。これは生産ライン工程で水酸化マグネシウムは
スラリー状で上がり、このとき表面処理剤を一括投入し
充分に攪拌処理を行ない、乾燥工程を行なうことももち
ろんできる。
It can also be processed in the magnesium hydroxide production line process. This is done in the production line process, where the magnesium hydroxide is produced in the form of a slurry, and at this time, the surface treatment agent can be added all at once, sufficiently stirred, and the drying process can of course be carried out.

(5)混合、混練方法 これらの各成分はそれぞれ計量混合され、従来のゴムプ
ラスチックのための装置と方法が利用でき特別の装置を
必要としない。すなわちリボンブレンダー、ヘンシェル
ミキサー等の混合攪拌機を用いて各成分を充分混合分散
させたのち、パンバリロール、押出機等の溶融混線機で
混練し目的物を得る。
(5) Mixing and kneading method These components are individually measured and mixed, and conventional equipment and methods for rubber plastics can be used, and no special equipment is required. That is, each component is sufficiently mixed and dispersed using a mixer such as a ribbon blender or a Henschel mixer, and then kneaded using a melt mixer such as a panburi roll or an extruder to obtain the desired product.

(6)成形 成形は、主に射出成形、押出成形等により、(5)で得
たペレットを具体的な形状、主にボックス型の収納ケー
スやジヨイントや、テープ状、チューブ状など任意の形
状の金型およびダイスを用いて成形できる。
(6) Molding is performed mainly by injection molding, extrusion molding, etc., to form the pellets obtained in (5) into specific shapes, mainly box-shaped storage cases, joints, tape shapes, tube shapes, etc. Can be molded using molds and dies.

〔発明の効果〕〔Effect of the invention〕

本発明はポリスチレン、ABS、ナイロン等の有害ガス
を発生する樹脂を使用せず、密度が0.92以下の低結
晶性の、α−オレフィンの重合体およびα−オレフィン
の共重合体を使用することによって、更には1種以上の
シランカップリング剤、シリコーン誘導体又は脂肪酸、
脂肪酸金属塩で表面処理した水酸化マグネシウムを使用
することによって、多量の水酸化マグネシウムを高充填
でき、燃焼向上の為にカーボンブラック等の炭素粉末を
使用することなしに、用途によって目的に応じた難燃性
およびカラーリングが可能であり、しかも非常に柔軟で
、低温特性および加工性に優れた難燃組成物を提供でき
るものである。
The present invention does not use resins that generate harmful gases such as polystyrene, ABS, and nylon, but uses low-crystalline α-olefin polymers and α-olefin copolymers with a density of 0.92 or less. Possibly also one or more silane coupling agents, silicone derivatives or fatty acids,
By using magnesium hydroxide whose surface has been treated with fatty acid metal salts, it is possible to charge a large amount of magnesium hydroxide, and it can be used in various ways depending on the purpose, without using carbon powder such as carbon black to improve combustion. It is possible to provide a flame-retardant composition that is flame-retardant and can be colored, is extremely flexible, and has excellent low-temperature properties and processability.

〔実施例〕〔Example〕

以下実施例をあげて説明する。 This will be explained below by giving examples.

実施例1〜7の各難燃性混和物を下記表1に従って各々
配合し、パンバリロールで溶融混練し目的物を得た。ま
た水酸化マグネシウムの表面処理は処理剤を加えてスー
パーミキサーで高速30分処理を行なった。次にチュー
ブ押出加工性、脆化温度、有害ガス成分、伸び、加熱変
形率、燃焼性の各特性を調べた。
Each of the flame-retardant mixtures of Examples 1 to 7 was blended according to Table 1 below, and melt-kneaded using a panburi roll to obtain the desired product. In addition, the surface treatment of magnesium hydroxide was carried out by adding a treating agent and performing high-speed treatment for 30 minutes in a super mixer. Next, the tube extrusion processability, embrittlement temperature, harmful gas components, elongation, thermal deformation rate, and combustibility were investigated.

これらの結果を表1に示す。These results are shown in Table 1.

Claims (2)

【特許請求の範囲】[Claims] (1)密度が0.92以下のα−オレフィンの単独重合
体又はα−オレフィンの共重合体樹脂100重量部に対
して、
(1) For 100 parts by weight of an α-olefin homopolymer or α-olefin copolymer resin having a density of 0.92 or less,
(2)1種以上のシランカップリング剤、シリコーン誘
導体又は脂肪酸、脂肪酸金属塩で表面処理した水酸化マ
グネシウム50〜250重量部を添加してなるオレフィ
ン系難燃樹脂組成物。
(2) An olefin flame-retardant resin composition containing 50 to 250 parts by weight of magnesium hydroxide surface-treated with one or more silane coupling agents, silicone derivatives, fatty acids, or fatty acid metal salts.
JP797486A 1986-01-20 1986-01-20 Flame-retardant resin composition Pending JPS62167339A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP797486A JPS62167339A (en) 1986-01-20 1986-01-20 Flame-retardant resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP797486A JPS62167339A (en) 1986-01-20 1986-01-20 Flame-retardant resin composition

Publications (1)

Publication Number Publication Date
JPS62167339A true JPS62167339A (en) 1987-07-23

Family

ID=11680430

Family Applications (1)

Application Number Title Priority Date Filing Date
JP797486A Pending JPS62167339A (en) 1986-01-20 1986-01-20 Flame-retardant resin composition

Country Status (1)

Country Link
JP (1) JPS62167339A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62212446A (en) * 1986-03-13 1987-09-18 Mitsui Petrochem Ind Ltd Vulcanizable rubber composition
JPH0238434A (en) * 1988-07-29 1990-02-07 Nippon Unicar Co Ltd Flame-retarding polyolefin resin composition
WO1998046673A1 (en) 1997-04-17 1998-10-22 Duslo, A.S. S^¿Ala A polymeric composite material with improved flame resistance
WO2005103138A1 (en) * 2004-04-20 2005-11-03 Yazaki Corporation Polyolefin resin composition and electric wires made by using the same
US7799857B2 (en) 2005-05-20 2010-09-21 Sun Allomer Ltd. Flame-retardant thermoplastic resin composition, molded product thereof and electric wire
US8313674B2 (en) 2004-08-11 2012-11-20 Sun Allomer Ltd. Flame-retardant polyolefin resin composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62212446A (en) * 1986-03-13 1987-09-18 Mitsui Petrochem Ind Ltd Vulcanizable rubber composition
JPH0238434A (en) * 1988-07-29 1990-02-07 Nippon Unicar Co Ltd Flame-retarding polyolefin resin composition
WO1998046673A1 (en) 1997-04-17 1998-10-22 Duslo, A.S. S^¿Ala A polymeric composite material with improved flame resistance
WO2005103138A1 (en) * 2004-04-20 2005-11-03 Yazaki Corporation Polyolefin resin composition and electric wires made by using the same
US8313674B2 (en) 2004-08-11 2012-11-20 Sun Allomer Ltd. Flame-retardant polyolefin resin composition
US7799857B2 (en) 2005-05-20 2010-09-21 Sun Allomer Ltd. Flame-retardant thermoplastic resin composition, molded product thereof and electric wire

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