JPS5931539B2 - Flame retardant resin composition - Google Patents

Flame retardant resin composition

Info

Publication number
JPS5931539B2
JPS5931539B2 JP311177A JP311177A JPS5931539B2 JP S5931539 B2 JPS5931539 B2 JP S5931539B2 JP 311177 A JP311177 A JP 311177A JP 311177 A JP311177 A JP 311177A JP S5931539 B2 JPS5931539 B2 JP S5931539B2
Authority
JP
Japan
Prior art keywords
weight
parts
flame retardant
flame
styrene
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
JP311177A
Other languages
Japanese (ja)
Other versions
JPS5388052A (en
Inventor
実 田華
紀之 関根
達行 三野
「あきら」 木下
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 Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP311177A priority Critical patent/JPS5931539B2/en
Priority to US05/866,905 priority patent/US4173561A/en
Publication of JPS5388052A publication Critical patent/JPS5388052A/en
Publication of JPS5931539B2 publication Critical patent/JPS5931539B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明はスチレン系樹脂にハロゲン系難燃剤のデカブロ
モジフェニルエーテルとマグネシウムの水酸化物、酸化
物又は塩基性炭酸マグネシウムおよび紫外線吸収剤とを
添加してなる難燃性にして且つ耐候性に優れた樹脂組成
物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a flame retardant material obtained by adding decabromodiphenyl ether, a halogen flame retardant, magnesium hydroxide, oxide or basic magnesium carbonate, and an ultraviolet absorber to a styrene resin. The present invention relates to a resin composition which also has excellent weather resistance.

従来からスチレン系樹脂は優れた加工性、機械5 的、
電気的特性、成型品の外観の美しさ等を有し、又価格も
安く、広<家庭電気機器類、家具類に使用されている。
Styrenic resins have traditionally had excellent processability, mechanical properties,
It has good electrical properties and a beautiful appearance as a molded product, and is also inexpensive, so it is widely used in household electrical equipment and furniture.

しかしながら、スチレン系樹脂は、はなはだ易燃性のた
め多くの使用土の制限を受けている。
However, styrenic resins are highly flammable and are subject to many restrictions in terms of where they can be used.

10近年火災に対する安全の必要性から、これらのスチ
レン系樹脂に対する難燃化の要求がとみにクローズアッ
プされ、米国アンダーライターズ、ラボラトリー規格(
以下UL規格と略称する)が年とともに強化されるに伴
ない、スチレン系樹脂の15難燃化が強く要望されてい
る。
10 In recent years, due to the need for fire safety, the demand for flame retardant properties for these styrenic resins has attracted attention, and the U.S. Underwriters and Laboratory Standards (
As the UL standards (hereinafter referred to as UL standards) have been strengthened over the years, there has been a strong demand for 15 flame retardant styrene resins.

かかるスチレン系樹脂に難燃性を付与するために難燃剤
と呼ばれる一連の化合物、例えば有機ハロゲン化合物、
リン酸ヱステル化合物、ハロゲンとリンの両者を含有す
る化合物、さらに三酸化ア20ンチモン等の難燃助剤を
添加する方法が知られており完全に不燃化にすることは
困難であるが遅燃性にしたり、自己消火性にすることが
可能である。
In order to impart flame retardancy to such styrenic resins, a series of compounds called flame retardants, such as organic halogen compounds,
Methods of adding flame retardant aids such as ester phosphoric acid compounds, compounds containing both halogen and phosphorus, and antimony trioxide are known, and although it is difficult to make them completely nonflammable, they do slow combustion. It is possible to make it self-extinguishing or self-extinguishing.

しかしこれらの方法によれば極めて多量の難燃剤を必要
とするため、耐候性が一様に低下し、紫外25線吸収剤
添加によつてもある程度は改良されるがとくに厳しい難
燃性たとえばUL規格のV−1、V−O相当を付与する
場合、不十分であり、淡色の成型品には好ましくないの
が実情である。このようにスチレン系樹脂をベースにし
た組成物につ30いては優れた難燃性および耐候性を兼
備させることは非常に困難である。本発明者らはスチレ
ン系樹脂の性質を損うことなくUL規格のV−1、V−
O相当の優れた難燃性および耐候性を得るのに、スチレ
ン系樹脂にハ35ロゲン系難燃剤のデカブロモジフェニ
ルエーテルと、マグネシウムの水酸化物、酸化物又は塩
基性炭酸マグネシウムよりなる群より選ばれた一種又は
二種以上の無機化合物および紫外線吸収剤を添加するの
が非常に好ましい結果を与えることを見出した。
However, these methods require an extremely large amount of flame retardant, which results in a uniform decline in weather resistance, and although it can be improved to some extent by adding an ultraviolet 25 ray absorber, particularly severe flame retardance, such as UL The reality is that when applying the standard V-1 and V-O equivalents, it is insufficient and undesirable for light-colored molded products. As described above, it is extremely difficult to provide compositions based on styrene resins with both excellent flame retardancy and weather resistance. The present inventors have developed V-1 and V- according to UL standards without impairing the properties of styrene resin.
In order to obtain excellent flame retardancy and weather resistance equivalent to O, the styrene-based resin is combined with decabromodiphenyl ether, a halogen-based flame retardant, and magnesium hydroxide, oxide, or basic magnesium carbonate. It has been found that the addition of one or more inorganic compounds and an ultraviolet absorber gives very favorable results.

すなわちハロゲン系難燃剤のデカプロモジフエニルエー
テルを加えることによつて難燃化が促進され、UL規格
のV−1,V−0相当が得られる。
That is, by adding decapromodiphenyl ether, which is a halogen-based flame retardant, flame retardancy is promoted, and a value equivalent to V-1 and V-0 of the UL standard is obtained.

またマグネシウムの水酸化物、酸化物又は塩基性炭酸マ
グネシウムよりなる群より選ばれた一種又は二種以上の
無機化合物を加えることにより、ハロゲン系難燃剤の添
加により低下した耐候性を著しく回復させる。以下に本
発明についてさらに詳細に説明する。
Furthermore, by adding one or more inorganic compounds selected from the group consisting of magnesium hydroxide, oxide, or basic magnesium carbonate, the weather resistance decreased by the addition of the halogen flame retardant can be significantly restored. The present invention will be explained in more detail below.

本発明でいうスチレン系樹脂とは、ポリスチレン、ゴム
変性ポリスチレン(以下HIポリスチレン樹脂と称す。
)、ポリメチルスチレン、スチレン−ブタジエン共重合
体、スチレン−アクリロニトリル共重合体(以下AS樹
脂と称す。)等又はこれらの混合物からなるものであり
、さらにこれらの樹脂にスチレン系樹脂としての特性を
損なわない範囲でポリブタジエンゴム又はスチレンブタ
ジエ トン共重合体ゴムなどのエラストマー性物質を添
加してなる樹脂組成物をも含有する。かかるスチレン系
樹脂に用いるハロゲン系難燃剤のデカプロモジフエニル
エーテルは、M.P.3OO℃,Brコンテント81%
の臭素系難燃剤 闘で市販されているいずれのものでも
良い。
The styrene resin referred to in the present invention refers to polystyrene and rubber-modified polystyrene (hereinafter referred to as HI polystyrene resin).
), polymethylstyrene, styrene-butadiene copolymer, styrene-acrylonitrile copolymer (hereinafter referred to as AS resin), etc., or a mixture thereof. It also contains a resin composition in which an elastomeric substance such as polybutadiene rubber or styrene-butadiene copolymer rubber is added to the extent that no damage is caused. Decabromodiphenyl ether, a halogen flame retardant used in such styrene resins, is disclosed by M. P. 3OO℃, Br content 81%
Any commercially available brominated flame retardant may be used.

本発明におけるデカプロモジフエニルエーテルはUL規
格V−1およびV−0相当の難燃性を少量の添加で得る
ことができ、且つ電気材料などとして耐熱性が重視され
る用途には優れた効果を発揮する。 3本発明において
、スチレン系樹脂とハロゲン系難燃剤のデカプロモジフ
エニルエーテルとの量的割合は前者100重量部に対し
、後者が11〜30重量部の範囲である。すなわちハロ
ゲン系難燃剤のデカプロモジフエニルエーテルの添加量
がスチ 3レン系樹脂100重量部に対して11重量部
未満では、得られる樹脂組成物の難燃性が十分でなく、
また30重量部をこえて添加しても難燃性はそれほど向
上せず逆に他の物性が損なわれる。本発明においてデカ
プロモジフエニルエーテル 4の好ましい添加量はV−
1相当の難燃性を得るには11〜14重量部であり、又
−0相当の難燃性を得るには15〜30重量部添加する
ことが好ましい。
The decapromodiphenyl ether of the present invention can obtain flame retardancy equivalent to UL standards V-1 and V-0 by adding a small amount, and has excellent effects in applications where heat resistance is important such as electrical materials. demonstrate. 3 In the present invention, the quantitative ratio of the styrene resin and the halogenated flame retardant decabromodiphenyl ether is in the range of 11 to 30 parts by weight to 100 parts by weight of the former. That is, if the amount of the halogen flame retardant decapromodiphenyl ether added is less than 11 parts by weight per 100 parts by weight of the styrene resin, the resulting resin composition will not have sufficient flame retardancy.
Furthermore, if more than 30 parts by weight is added, the flame retardance will not improve much, but other physical properties will be impaired. In the present invention, the preferred amount of decapromodiphenyl ether 4 is V-
It is preferable to add 11 to 14 parts by weight to obtain a flame retardance equivalent to 1, and 15 to 30 parts by weight to obtain a flame retardance equivalent to -0.

本発明においては、ハロゲン系難燃剤単独でも良好な効
果が得られるが、さらに三酸化アンチモンや二酸化ジル
コニウムなどの難燃助剤を併用することによつて一層難
燃性を向上させることができるので好ましい。
In the present invention, a good effect can be obtained using a halogen-based flame retardant alone, but flame retardancy can be further improved by using a flame retardant aid such as antimony trioxide or zirconium dioxide in combination. preferable.

このような難燃助剤の添加量はスチレン系樹脂100重
量部に対し1重量部未満では難燃助剤効果が十分でなく
、また10重量部をこえて添加しても難燃助剤効果はそ
れ以上には向上せず、逆に他の物性が損なわれる場合が
ある。さらに本発明に用いる無機化合物とは、水酸化マ
グネシウム、酸化マグネシウム又は塩基性炭酸マグネシ
ウムをあげることができるが、特に好ましい無機化合物
は水酸化マグネシウムおよび酸化マグネシウムであり、
著しく耐候性を改良するのである。
If the amount of such flame retardant aid added is less than 1 part by weight per 100 parts by weight of the styrene resin, the flame retardant aid effect will not be sufficient, and if it is added in excess of 10 parts by weight, the flame retardant aid effect will not be sufficient. is not improved any further, and on the contrary, other physical properties may be impaired. Further, the inorganic compounds used in the present invention include magnesium hydroxide, magnesium oxide, and basic magnesium carbonate, and particularly preferred inorganic compounds are magnesium hydroxide and magnesium oxide.
It significantly improves weather resistance.

本発明においてスチレン系樹脂とマグネシウムの水酸化
物、酸化物又は塩基性炭酸マグネシウムよりなる群より
選ばれた一種又は二種以上の無機化合物との量的割合は
前者100重量部に対して後者が0.1〜10重量部の
範囲が適当である。
In the present invention, the quantitative ratio of the styrene resin and one or more inorganic compounds selected from the group consisting of magnesium hydroxide, oxide, or basic magnesium carbonate is such that the latter is 100 parts by weight of the former. A range of 0.1 to 10 parts by weight is suitable.

すなわち、スチレン系樹脂100重量部に対し、0.1
重量部未満では耐候性の改良は不十分であり、10重量
部をこえて添加すると逆に耐候性が低下したり、又他の
物性が損なわれる。本発明に用いる紫外線吸収剤は、ベ
ンゾトリアゾール系、ベンゾフエノン系、サリシレート
系等又はこれらの配合物いずれでも良好な効果が得られ
る。
That is, for 100 parts by weight of styrene resin, 0.1
If it is less than 10 parts by weight, the improvement in weather resistance will be insufficient, and if it is added in excess of 10 parts by weight, weather resistance will deteriorate or other physical properties will be impaired. The ultraviolet absorber used in the present invention may be benzotriazole-based, benzophenone-based, salicylate-based, etc., or any combination thereof, and good effects can be obtained.

例えばベンゾトリアゾール系では、2−(21−ヒドロ
キシ−5′−メチルフエニル)ベンゾトリアゾール、2
−(2′−ヒドロキシ−5′−ターシヤリーブチルフエ
ニル)ベンゾトリアゾール、2−(27−ヒドロキシ−
3′,5′−ジターシヤリーブチルーフエニル)−5−
クロロベンゾトリアゾールなどがあげられる。ベンゾフ
エノン系では2−ヒドロキシ−4−メトキシベンゾフエ
ノン、2,2′−ジーヒドロキシ一4−メトキシベンゾ
フエノン等、サリシレート系ではフエニルサリシレート
、4−オクチルフエニルサリシレート等をあげることが
できる。
For example, in the benzotriazole series, 2-(21-hydroxy-5'-methylphenyl)benzotriazole, 2
-(2'-hydroxy-5'-tert-butylphenyl)benzotriazole, 2-(27-hydroxy-
3',5'-ditertiarybutyrulfenyl)-5-
Examples include chlorobenzotriazole. Examples of the benzophenone type include 2-hydroxy-4-methoxybenzophenone and 2,2'-dihydroxy-14-methoxybenzophenone, and examples of the salicylate type include phenyl salicylate and 4-octylphenyl salicylate.

本発明において紫外線吸収剤の添加量は0.1〜5重量
部の範囲が適当である。すなわち、スチレン系樹脂10
0重量部に対して0.1重量部未満では耐候性の改良は
不十分であり、5重量部をこえて添加しても耐候性の改
良はそれ以上には向上せず逆に難燃性などの物性を低下
させる。
In the present invention, the amount of the ultraviolet absorber added is suitably in the range of 0.1 to 5 parts by weight. That is, styrene resin 10
If it is less than 0.1 parts by weight, the improvement in weather resistance is insufficient, and if more than 5 parts by weight is added, the improvement in weather resistance will not be further improved, and on the contrary, the flame retardancy will be improved. and other physical properties.

このように本発明での難燃性樹脂組成物中におけるマグ
ネシウムの水酸化物、酸化物又は塩基性炭酸マグネシウ
ムよりなる群より選ばれた一種又は二種以上の無機化合
物および紫外線吸収剤との組合せは難燃剤による耐候性
低下を著しく改良しているのである。本発明において特
に効果のあるV−1,V−0組成物の組み合せはデカプ
ロモジフエニルエーテル、三酸化アンチモン、水酸化マ
グネシウム又は酸化マグネシウムおよび紫外線吸収剤チ
ヌピン327(チバガイギ一製)の系であり著しく耐候
性を改良している。
In this way, the combination of one or more inorganic compounds selected from the group consisting of magnesium hydroxide, oxide, or basic magnesium carbonate and an ultraviolet absorber in the flame-retardant resin composition of the present invention This significantly improves the deterioration in weather resistance caused by flame retardants. A combination of V-1 and V-0 compositions that is particularly effective in the present invention is a system of decapromodiphenyl ether, antimony trioxide, magnesium hydroxide or magnesium oxide, and the ultraviolet absorber Tinupin 327 (manufactured by Ciba Geigi). Weather resistance is significantly improved.

本発明の難燃性樹脂組成物に従来よりスチレン系樹脂に
用いられている種々の添加剤、例えば抗酸化剤、滑剤、
帯電防止剤或は染顔料等を適宜添加することは何ら差支
えない。
The flame retardant resin composition of the present invention contains various additives conventionally used in styrenic resins, such as antioxidants, lubricants,
There is no problem in adding antistatic agents, dyes and pigments as appropriate.

本発明の難燃性樹脂組成物は種々の方法で得ることがで
きる。
The flame-retardant resin composition of the present invention can be obtained by various methods.

例えば前記したスチレン系樹脂とハロゲン系難燃剤、難
燃助剤、あるいは添加剤と共に通常の方法、例えばリポ
ンプレンダ一、ドラムブレンダ一、ペンシェルミキサー
等の混合機を用いて混合することにより、あるいは更に
熱ロール、ベンバリーミキサ一、押出機で熔融混練する
ことにより得られる。このようにして得られた本発明の
難燃性樹脂組成物は、従来公知の成型加工法、例えば射
出成形法、押出成形法などによつて各種形状の成形物に
容易に成形加工出来るとともに、このようにして得られ
る成形物は従来の難燃性スチレン系樹脂に比して難燃性
、耐候性の総合的特性に関し、格段に優れている。以下
に本発明の有用性を実施例によりさらに詳しく説明する
が、本発明はこれらの実施例に限定されるものではない
0実施例 1 ゴム変性ポリスチレン樹脂ビーズエスブライト500H
Mビーズ(日本ポリスチレン製)とスチレンブタジエン
共重合体ゴムタブプレン(旭化成製)とプラネロンDB
−101(三井東圧フアイン製)、三酸化アンチモン(
住友金属鉱山製)、水酸化マグネシウム(協和化学製)
、酸化マグネシウム(半井化学製)、塩基性炭酸マグネ
シウム(半井化学製)およびチヌピン327(チバガイ
ギ一製)とをそれぞれ第1表に示す量を先ず攪拌型混合
機により予備混合を行ない、スクリユ一直径40mmφ
の押出機によりシリンダー温度200℃、スクリユ一回
転数40rpmの条件下で加熱混合し、ペレツト化した
For example, by mixing the above-mentioned styrene resin with a halogen flame retardant, a flame retardant aid, or an additive in a conventional manner, for example, using a mixer such as a lipon blender, a drum blender, a pen shell mixer, or further. It is obtained by melt-kneading using a heated roll, a Benbury mixer, and an extruder. The flame-retardant resin composition of the present invention thus obtained can be easily molded into molded articles of various shapes by conventionally known molding methods, such as injection molding and extrusion molding. The molded product obtained in this manner is far superior to conventional flame-retardant styrene resins in terms of comprehensive properties such as flame retardancy and weather resistance. The usefulness of the present invention will be explained in more detail by Examples below, but the present invention is not limited to these Examples.Example 1 Rubber-modified polystyrene resin beads S-Brite 500H
M beads (manufactured by Nippon Polystyrene), styrene-butadiene copolymer rubber tabrene (manufactured by Asahi Kasei), and Planelon DB
-101 (manufactured by Mitsui Toatsu Fine), antimony trioxide (
(manufactured by Sumitomo Metal Mining), magnesium hydroxide (manufactured by Kyowa Chemical)
, magnesium oxide (manufactured by Hanui Chemicals), basic magnesium carbonate (manufactured by Hansui Chemicals), and Tinupin 327 (manufactured by Ciba-Geigi Co., Ltd.) in the amounts shown in Table 1 were first premixed using an agitating mixer. 40mmφ
The mixture was heated and mixed using an extruder at a cylinder temperature of 200° C. and a screw rotation speed of 40 rpm to form pellets.

このペレツトを3オンスインライン式射出成形機により
シリンダー温度200℃で射出成形を行ない、燃焼試験
片、ウエザ一照射試験片を作成し、各々の試験に供した
。得られた結果をまとめて第1表に示す。第1表から明
らかなようにスチレン系樹脂にデカプロモジフエニルエ
ーテル、水酸化マグネシウム、酸化マグネシウム又は塩
基性炭酸マグネシウムおよび紫外線吸収剤とを共に添加
すると、耐候性は著しく向上し、且つ難燃性に優れる。
The pellets were injection molded using a 3-ounce in-line injection molding machine at a cylinder temperature of 200°C to prepare combustion test pieces and weather-irradiation test pieces, which were used for each test. The results obtained are summarized in Table 1. As is clear from Table 1, when decabromodiphenyl ether, magnesium hydroxide, magnesium oxide or basic magnesium carbonate, and an ultraviolet absorber are added to styrenic resin, weather resistance is significantly improved and flame retardancy is improved. Excellent in

実施例 2〜3 ゴム変性ポリスチレン樹脂ビーズエスプライト500H
Mビーズ(日本ポリスチレン製)とスチレンブタジエン
共重合ゴムタブプレン(旭化成製)とプラネロンDB−
101(三井東圧フアイン製)、三酸化アンチモン(住
友金属鉱山製)、水酸化マグネシウム(協和化学製)お
よびチヌピン327(チバガイギ一製)とをそれぞれ第
2表〜第3表に示す割合で実施例1と同様の方法によつ
て混合し、それぞれの所定の試験片を作成し、試験に供
した。
Examples 2-3 Rubber modified polystyrene resin beads Esprite 500H
M beads (manufactured by Nippon Polystyrene), styrene-butadiene copolymer rubber tabrene (manufactured by Asahi Kasei), and Planelon DB-
101 (manufactured by Mitsui Toatsu Fine), antimony trioxide (manufactured by Sumitomo Metal Mining), magnesium hydroxide (manufactured by Kyowa Chemical Co., Ltd.) and Tinupin 327 (manufactured by Ciba-Geigi Co., Ltd.) in the proportions shown in Tables 2 and 3, respectively. The mixtures were mixed in the same manner as in Example 1, and predetermined test pieces were prepared for each test piece.

得られた結果をまとめて第2表〜第3表に示す。The obtained results are summarized in Tables 2 to 3.

第2表より明らかなようにスチレン系樹脂と水酸化マグ
ネシウムの量的割合が前者100重量部に対して、後者
が0.1〜10重量部の範囲において耐候性の改良が行
なわれ、且つ難燃性に優れている。さらに第3表より明
らかなように、スチレン系樹脂と紫外線吸収剤との量的
割合が前者100重量部に対して後者が0.1〜5重量
部の範囲において耐候性の改良が行なわれ、且つ難燃性
に優れている。
As is clear from Table 2, weather resistance is improved when the quantitative ratio of styrene resin and magnesium hydroxide is in the range of 0.1 to 10 parts by weight relative to 100 parts by weight of the former. Excellent flammability. Furthermore, as is clear from Table 3, the weather resistance is improved when the quantitative ratio of the styrene resin and the ultraviolet absorber is in the range of 0.1 to 5 parts by weight to 100 parts by weight of the former, It also has excellent flame retardancy.

Claims (1)

【特許請求の範囲】[Claims] 1 アクリロニトリル−ブタジエン−スチレン共重合体
樹脂を除くスチレン系樹脂100重量部に対して、(1
)ハロゲン系難燃剤のデカブロモジフェニルエーテル1
1〜30重量部、(2)マグネシウムの水酸化物、酸化
物又は塩基性炭酸マグネシウムよりなる群より選ばれた
一種又は二種以上の無機化合物0.1〜10重量部、お
よび(3)紫外線吸収剤0.1〜5重量部を配合してな
る耐候性に優れた難燃性樹脂組成物。
1 For 100 parts by weight of styrene resin excluding acrylonitrile-butadiene-styrene copolymer resin, (1
) Halogenated flame retardant decabromodiphenyl ether 1
1 to 30 parts by weight, (2) 0.1 to 10 parts by weight of one or more inorganic compounds selected from the group consisting of magnesium hydroxide, oxide, or basic magnesium carbonate, and (3) ultraviolet rays. A flame-retardant resin composition with excellent weather resistance, which contains 0.1 to 5 parts by weight of an absorbent.
JP311177A 1977-01-12 1977-01-13 Flame retardant resin composition Expired JPS5931539B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP311177A JPS5931539B2 (en) 1977-01-13 1977-01-13 Flame retardant resin composition
US05/866,905 US4173561A (en) 1977-01-12 1978-01-04 Flame retardant polymer composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP311177A JPS5931539B2 (en) 1977-01-13 1977-01-13 Flame retardant resin composition

Publications (2)

Publication Number Publication Date
JPS5388052A JPS5388052A (en) 1978-08-03
JPS5931539B2 true JPS5931539B2 (en) 1984-08-02

Family

ID=11548230

Family Applications (1)

Application Number Title Priority Date Filing Date
JP311177A Expired JPS5931539B2 (en) 1977-01-12 1977-01-13 Flame retardant resin composition

Country Status (1)

Country Link
JP (1) JPS5931539B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03103839U (en) * 1990-02-09 1991-10-29

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2678359B2 (en) * 1987-10-14 1997-11-17 大日本インキ化学工業株式会社 Flame retardant resin composition
JPH0364346A (en) * 1989-08-03 1991-03-19 Mitsui Toatsu Chem Inc Lowly corrosive flame-retarding resin composition
JP2014152298A (en) * 2013-02-13 2014-08-25 Yazaki Corp Resin composition and coated electric wire using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03103839U (en) * 1990-02-09 1991-10-29

Also Published As

Publication number Publication date
JPS5388052A (en) 1978-08-03

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