JPH1160854A - Styrene resin composition and electrical or electronic appliance housing made therefrom - Google Patents

Styrene resin composition and electrical or electronic appliance housing made therefrom

Info

Publication number
JPH1160854A
JPH1160854A JP22263397A JP22263397A JPH1160854A JP H1160854 A JPH1160854 A JP H1160854A JP 22263397 A JP22263397 A JP 22263397A JP 22263397 A JP22263397 A JP 22263397A JP H1160854 A JPH1160854 A JP H1160854A
Authority
JP
Japan
Prior art keywords
flame retardant
fiber
resin composition
weight
styrene resin
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
JP22263397A
Other languages
Japanese (ja)
Inventor
Takekazu Shinagawa
剛数 品川
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.)
Idemitsu Petrochemical Co Ltd
Original Assignee
Idemitsu Petrochemical 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 Idemitsu Petrochemical Co Ltd filed Critical Idemitsu Petrochemical Co Ltd
Priority to JP22263397A priority Critical patent/JPH1160854A/en
Publication of JPH1160854A publication Critical patent/JPH1160854A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain a composition excellent in the appearance of a molding and in heat stability during molding by mixing a styrene resin with an organic fiber having a specified fiber diameter and a specified fiber length and a dispersant in a specified ratio. SOLUTION: One hundred pts.wt. styrene resin is mixed with 0.1-2 pts.wt. organic fiber having a fiber diameter of 5-100 μm and a fiber length of 0.01-2 mm and 0.1-3 pts.wt. dispersant. The styrene resin is obtained for example by dissolving a rubbery polymer (e.g. polybutadiene) in a vinylaromatic monomer (e.g. styrene) in the presence of a comonomer (e.g. acrylonitrile), subjecting the solution to bulk polymerization or the like to deposit the rubbery polymer on the matrix. The organic fiber used is desirably for example rayon, polyester and nylon fibers. The dispersant is exemplified by a higher fatty acid, its metal salt or an fatty acid ester. The flame retardant used is exemplified by a bromine-containing flame retardant (e.g. brominated bisphenol epoxy polymer).

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、新規なスチレン系
樹脂組成物およびそれを用いた成形品に関するもので、
詳しくは、成形外観及び成形時の熱安定性にすぐれたス
チレン系樹脂組成物及びそれらを成形材料として使用し
た電気又は電子機器製品用ハウジングに関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel styrenic resin composition and a molded article using the same.
More specifically, the present invention relates to a styrenic resin composition having excellent molding appearance and thermal stability at the time of molding, and a housing for electric or electronic equipment products using the same as a molding material.

【0002】[0002]

【従来の技術】従来、ポリスチレン、ABS樹脂等のス
チレン系樹脂は、優れた成形加工性、機械的強度、電気
特性を有していることから、多くの分野で使用されてい
るが、テレビキャビネット等の電気又は電子機器ハウジ
ングでは成形時の外観不良を補い、耐光性を改良するた
め、表面塗装が通常行われている。
2. Description of the Related Art Hitherto, styrene resins such as polystyrene and ABS resin have been used in many fields because of their excellent moldability, mechanical strength and electrical properties. Surface coating is usually performed on electric or electronic equipment housings such as those described above to compensate for poor appearance during molding and improve light resistance.

【0003】しかし、表面塗装は作業工程の増加をもた
らし、又環境保護のために製品をリサイクルする際、塗
装膜の存在はリサイクルを困難にする。そこで、近年製
品のリサイクル及びコストダウンのため、電気又は電子
機器ハウジングの無塗装化のニ−ズが高まっている。し
かしながら、ウエルド部の外観不良や成形時の熱安定性
不良(具体的にはシルバ−の発生)の問題が未解決のた
め無塗装化は実際的には困難であった。
[0003] However, surface coating results in an increase in the number of working steps, and the presence of a coating film makes recycling difficult when recycling products for environmental protection. Therefore, in recent years, there has been an increasing demand for unpainted electrical or electronic equipment housings in order to recycle products and reduce costs. However, since the problems of poor appearance of the weld portion and poor thermal stability at the time of molding (specifically, generation of silver) have not been solved, it is practically difficult to remove the coating.

【0004】[0004]

【発明が解決しようとする課題】本発明は、スチレン系
樹脂組成物成形品における上記問題を解決し、ウエルド
部の製品外観及び成形時の熱安定性が改良されたスチレ
ン系樹脂組成物及びそれを使用した無塗装化が可能な電
気又は電子機器ハウジングを提供することを目的とす
る。
DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned problems in a styrenic resin composition molded article, and provides a styrenic resin composition having improved weld appearance and heat stability at the time of molding. It is an object of the present invention to provide an electric or electronic equipment housing that can be made unpainted by using an electronic component.

【0005】[0005]

【課題を解決するための手段】本発明者らは、上記課題
につき鋭意検討した結果、特定の有機繊維と分散剤を使
用することによりこの課題を解決できること、さらには
難燃剤と難燃助剤を特定量加えることにより難燃性と諸
物性のバランスもすぐれた組成物となることを見出し、
この知見に基づいて下記内容を要旨とする本発明を完成
させた。
Means for Solving the Problems As a result of intensive studies on the above problems, the present inventors have found that this problem can be solved by using a specific organic fiber and a dispersant, and furthermore, a flame retardant and a flame retardant auxiliary agent. By adding a specific amount of, it is found that the composition is also excellent in flame retardancy and various physical properties,
Based on this knowledge, the present invention having the following contents has been completed.

【0006】(1)(A)スチレン系樹脂100重量部
に対して、(B)繊維径が5〜100ミクロンで繊維長
が0.01〜2mmの有機繊維0.1〜2重量部、
(C)分散剤0.1〜3重量部を配合してなるスチレン
系樹脂組成物。 (2)(B)有機繊維がレ−ヨン系、ポリエステル系又
はナイロン系繊維である(1)に記載のスチレン系樹脂
組成物。 (3)(C)分散剤が高級脂肪酸又はその金属塩である
(1)又は(2)に記載のスチレン系樹脂組成物。 (4)スチレン系樹脂100重量部に対して、さらに
(D)難燃剤3〜30重量部、及び(E)難燃助剤2〜
10重量部を配合してなる(1)〜(3)のいずれかに
記載のスチレン系樹脂組成物。 (5)(D)難燃剤が臭素化ビスフェノ−ル型エポキシ
重合体、ポリハロゲン化ジフェニルアルカン、臭素化ト
リアジン、ポリメチルフェニルインデン系難燃剤のうち
の少なくとも1種類である(4)記載のスチレン系樹脂
組成物。 (6)(1)〜(5)のいずれかに記載のスチレン系樹
脂組成物を成形してなる電気又は電子機器製品用ハウジ
ング。
(1) 100 parts by weight of (A) styrene resin, (B) 0.1 to 2 parts by weight of organic fibers having a fiber diameter of 5 to 100 microns and a fiber length of 0.01 to 2 mm,
(C) A styrenic resin composition containing 0.1 to 3 parts by weight of a dispersant. (2) The styrene resin composition according to (1), wherein the (B) organic fiber is a rayon-based, polyester-based or nylon-based fiber. (3) The styrene resin composition according to (1) or (2), wherein (C) the dispersant is a higher fatty acid or a metal salt thereof. (4) 100 parts by weight of styrene resin, (D) 3 to 30 parts by weight of flame retardant and (E) 2 to 3 parts by weight of flame retardant
The styrenic resin composition according to any one of (1) to (3), wherein 10 parts by weight are blended. (5) The styrene according to (4), wherein (D) the flame retardant is at least one of a brominated bisphenol-type epoxy polymer, a polyhalogenated diphenylalkane, a brominated triazine, and a polymethylphenylindene flame retardant. -Based resin composition. (6) A housing for an electric or electronic device product obtained by molding the styrene resin composition according to any one of (1) to (5).

【0007】[0007]

【発明の実施の形態】以下、本発明について詳細に説明
する。本発明に用いる(A)スチレン系樹脂は、特に制
限はなく公知の方法、例えばビニル芳香族単量体を単独
で又はコモノマ−共存下で重合させるか又はこれらに各
種ゴム状重合体を溶解させて、塊状重合、塊状懸濁重
合、懸濁重合等を行い、ビニル芳香族重合体単体又はマ
トリックス中にゴム状重合体を析出させた重合体を得、
粒子化することにより得られる。ここで用いるビニル芳
香族単量体としては、スチレン、o−メチルスチレン、
p−メチルスチレン、m−メチルスチレン、2,4−ジ
メチルスチレン、p−タ−シャリーブチルスチレン等核
アルキル置換スチレン、α−メチルスチレン、α−メチ
ル−p−メチルスチレン等のα−アルキル置換スチレン
等を挙げることができる。この中でも、スチレンを好適
に用いることができる。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. The styrenic resin (A) used in the present invention is not particularly limited, and is a known method, for example, a method in which a vinyl aromatic monomer is polymerized alone or in the presence of a comonomer, or various rubbery polymers are dissolved therein. By performing bulk polymerization, bulk suspension polymerization, suspension polymerization, etc., to obtain a polymer obtained by precipitating a rubber-like polymer in a vinyl aromatic polymer alone or in a matrix,
Obtained by forming particles. As the vinyl aromatic monomer used here, styrene, o-methylstyrene,
α-alkyl-substituted styrenes such as p-methylstyrene, m-methylstyrene, 2,4-dimethylstyrene, nucleated alkyl-substituted styrenes such as p-tert-butylstyrene, α-methylstyrene and α-methyl-p-methylstyrene And the like. Among them, styrene can be suitably used.

【0008】コモノマ−としては、アクリロニトリル、
無水マレイン酸等があげられる。前記ゴム状重合体とし
ては、ポリブタジエン、スチレン・ブタジエン共重合
体、ポリイソプレン等各種共役ジエン化合物、天然ゴム
等を挙げることができる。この中でも、ポリブタジエ
ン、スチレン・ブタジエン共重合体を好適に用いること
ができる。具体的には、スチレン系樹脂は、ホモポリス
チレン、ポリパラメチルスチレン、ゴム変性ポリスチレ
ン、ABS樹脂、AS樹脂、MBS樹脂、AES樹脂等
であり、特にゴム変性ポリスチレンを好適に用いること
ができる。ゴム変性ポリスチレンを用いる場合は、マト
リックス成分の重量平均分子量が、80,000〜35
0,000、ゴム添加量が5〜20重量%に調整された
ものが製品物性の点から好ましい。
[0008] As comonomer, acrylonitrile,
And maleic anhydride. Examples of the rubbery polymer include various conjugated diene compounds such as polybutadiene, styrene / butadiene copolymer, polyisoprene, and natural rubber. Among them, polybutadiene and styrene / butadiene copolymer can be preferably used. Specifically, the styrene-based resin is homopolystyrene, polyparamethylstyrene, rubber-modified polystyrene, ABS resin, AS resin, MBS resin, AES resin, etc., and rubber-modified polystyrene can be particularly preferably used. When rubber-modified polystyrene is used, the weight average molecular weight of the matrix component is 80,000 to 35.
It is preferable from the viewpoint of the physical properties of the product that the content of the rubber is adjusted to 0000 and the amount of the rubber added to 5 to 20% by weight.

【0009】(B)有機繊維としては所定の繊維径と繊
維長を有するものであれば、特に制限することなく使用
でき、具体的には、綿、絹、カボック、羊毛、亜麻、大
麻、ラミ、ジュ−ト、椰子などの天然繊維、ポリエステ
ル、ナイロン、ポリアセタ−ル、ポリウレタン、ポリエ
チレン、ポリ塩化ビニル、アクリル、アラミドなどの合
成繊維、アセテ−ト等の半合成繊維及びレ−ヨン、ビニ
ロン等の再生繊維があげられこれらを単独でもしくは組
合せて使用することも可能である。
(B) Any organic fiber having a predetermined fiber diameter and fiber length can be used without any particular limitation. Specifically, cotton, silk, kabok, wool, flax, hemp, lami , Jute, natural fiber such as coconut, polyester, nylon, polyacetal, polyurethane, polyethylene, polyvinyl chloride, acrylic, aramid, etc., semi-synthetic fiber such as acetate, rayon, vinylon, etc. And recycled fibers can be used alone or in combination.

【0010】これらのうち、レ−ヨン系、ポリエステル
系及びナイロン系繊維が汎用的に入手が容易なこと及び
必要な特性が得られ易いことから好適である。またレ−
ヨン、ビニロン、ポリエステル、アセテ−ト等の繊維は
延伸することにより絹のような光沢を備えた着色を呈し
これを用いてパ−ル状の色調をだすことも可能である。
又黄麻などの糸を染色したり、艶消し糸を使用すること
により艶消しの色調を成形品に出すこともできる。
Of these, rayon-based, polyester-based, and nylon-based fibers are preferred because they are easily available for general use and easily obtain required characteristics. In addition,
Fibers such as yong, vinylon, polyester, acetate and the like exhibit a silky coloring by stretching, and can be used to give a pearl-like color tone.
Further, by dyeing a yarn such as jute or using a matting yarn, a matte color tone can be obtained on a molded product.

【0011】本発明においては、このような有機繊維
は、繊維径が5〜100ミクロンでありかつ繊維長が
0.01〜2mmであることが必要である。ここでいう
繊維径とは繊維断面における最大径をいう。この範囲よ
り小さい繊維径もしくは短い繊維長のものは成形品の傷
つきが目立ちやすく好ましくなく、又この範囲より大き
い繊維径もしくは長い繊維長のものは、成形品のウエル
ドが目立ち良外観の製品が得られない。添加量は、スチ
レン系樹脂100重量部に対して0.1〜2重量部とす
る。0.1重量部未満の場合ウエルド外観の改良効果は
得られず、又2重量部以上では良好なウエルド外観の製
品が得られない恐れがあり好ましくない。
In the present invention, such an organic fiber needs to have a fiber diameter of 5 to 100 microns and a fiber length of 0.01 to 2 mm. Here, the fiber diameter refers to the maximum diameter in the fiber cross section. A fiber having a fiber diameter or a shorter fiber length smaller than this range is not preferable because the molded article is easily damaged, and a fiber having a fiber diameter or a longer fiber length larger than this range has a good appearance of the molded article and a good appearance. I can't. The addition amount is 0.1 to 2 parts by weight based on 100 parts by weight of the styrene resin. If the amount is less than 0.1 part by weight, the effect of improving the appearance of the weld cannot be obtained.

【0012】(C)分散剤とは、一般にスチレン系樹脂
への他の添加剤(有機繊維等)の分散性を高める働きの
ある添加剤であれば特に問題はなく、例えば高級脂肪酸
及びその金属塩、脂肪酸エステル、脂肪酸アミド、高級
アルコ−ル、ミネラルオイル、ポリエチレンワックス、
ポリエチレングリコ−ルなどがあげられる。好ましく
は、高級脂肪酸及び又はその金属塩であり、更に好まし
くは高級脂肪酸の亜鉛、マグネシウム、カルシウム、バ
リウムの金属塩である。
(C) The dispersant is not particularly limited as long as it is an additive which generally has an effect of improving the dispersibility of other additives (organic fibers and the like) in the styrene resin. Salt, fatty acid ester, fatty acid amide, higher alcohol, mineral oil, polyethylene wax,
Polyethylene glycol and the like. Preferred are higher fatty acids and / or metal salts thereof, and more preferable are zinc, magnesium, calcium and barium metal salts of higher fatty acids.

【0013】これら分散剤は、単独で又は2種以上を組
み合わせて使用することができ、その添加量はスチレン
系樹脂100重量部に対し、0.1〜3重量部の範囲で
ある。このような分散剤の添加量が0.1重量部未満で
ある場合には繊維同士の絡み合いを防ぐのが難しくな
り、良外観が得られなくなる。又添加量が3重量部を超
える場合、成形時に熱安定性不良のためシルバ−による
外観不良が発生し易くなる。本発明においては、特に難
燃性が要求される場合には、(D)難燃剤と(E)難燃
助剤をさらに配合する。(D)難燃剤としては、UL規
格等の難燃規制を満足させる目的でハロゲン系難燃剤が
好ましく使用される。ハロゲン系難燃剤としては塩素系
難燃剤、臭素系難燃剤及びフッ素系難燃剤が代表的なも
のであるが、中でも塩素系難燃剤及び臭素系難燃剤がよ
り好ましく、臭素系難燃剤が最も好適に使用される。
These dispersants can be used alone or in combination of two or more, and the amount added is in the range of 0.1 to 3 parts by weight based on 100 parts by weight of the styrene resin. If the amount of such a dispersant is less than 0.1 part by weight, it becomes difficult to prevent entanglement of the fibers, and a good appearance cannot be obtained. If the amount exceeds 3 parts by weight, poor appearance due to silver tends to occur due to poor thermal stability during molding. In the present invention, particularly when flame retardancy is required, (D) a flame retardant and (E) a flame retardant auxiliary are further blended. As the flame retardant (D), a halogen-based flame retardant is preferably used for the purpose of satisfying the flame retardant regulations such as UL standards. Representative examples of the halogen-based flame retardant include a chlorine-based flame retardant, a bromine-based flame retardant, and a fluorine-based flame retardant. Among them, the chlorine-based flame retardant and the brominated flame retardant are more preferred, and the brominated flame retardant is most preferred. Used for

【0014】通常、臭素系難燃剤としては臭素化ビスフ
ェノ−ル型エポキシ重合体、ポリハロゲン化ジフェニル
アルカン、臭素化トリアジン系難燃剤、ポリメチルフェ
ニルインデン系難燃剤、テトラブロモビスフェノ−ルA
等をあげることができる。塩素系難燃剤としてはパ−ク
ロロシクロペンタデカン、塩素化パラフィン等を例示で
きるが、本発明において特定のハロゲン系難燃剤の臭素
化ビスフェノ−ル型エポキシ重合体、ポリハロゲン化ジ
フェニルアルカン、臭素化トリアジン系難燃剤、及びポ
リメチルフェニルインデン系難燃剤から選ばれる少なく
とも一種の難燃剤が好適に用いられる。
Usually, brominated flame retardants include brominated bisphenol type epoxy polymer, polyhalogenated diphenylalkane, brominated triazine flame retardant, polymethylphenylindene flame retardant, tetrabromobisphenol A
Etc. can be given. Examples of the chlorine-based flame retardant include perchlorocyclopentadecane, chlorinated paraffin and the like. In the present invention, brominated bisphenol-type epoxy polymers, polyhalogenated diphenylalkanes, and brominated triazines as specific halogen-based flame retardants are used. At least one kind of flame retardant selected from a series flame retardant and a polymethylphenylindene flame retardant is preferably used.

【0015】配合量は、スチレン系樹脂100重量部に
対して、3〜30重量部であり、好ましくは10〜25
重量部である。ここで難燃剤の配合量が3重量部未満で
は、目的とする難燃向上効果が不十分となり、逆に30
重量部を超えると成形品の耐光性、耐衝撃性が低下し外
観も悪くなる。
The compounding amount is 3 to 30 parts by weight, preferably 10 to 25 parts by weight, per 100 parts by weight of the styrene resin.
Parts by weight. If the compounding amount of the flame retardant is less than 3 parts by weight, the intended effect of improving the flame retardant becomes insufficient.
If the amount exceeds the weight part, the light resistance and impact resistance of the molded product are reduced, and the appearance is deteriorated.

【0016】(E)難燃助剤は、難燃剤の難燃効果を向
上するために用いられ、具体的には三酸化アンチモン、
四酸化アンチモン、五酸化アンチモン、アンチモン酸ソ
ーダ、金属アンチモン、三塩化アンチモン、五塩化アン
チモン等のアンチモン系難燃助剤のほか、メタホウ酸バ
リウム、酸化ジルコニウム、ホウ酸亜鉛、スズ酸亜鉛等
を挙げることができる。これらの難燃助剤は単独で又は
2種以上組み合わせて使用することができる。これらの
中でも、特に三酸化アンチモンを好適に用いることがで
きる。
(E) The flame retardant aid is used for improving the flame retardant effect of the flame retardant. Specifically, antimony trioxide,
In addition to antimony-based flame retardants such as antimony tetroxide, antimony pentoxide, sodium antimonate, metal antimony, antimony trichloride, and antimony pentachloride, barium metaborate, zirconium oxide, zinc borate, zinc stannate, etc. be able to. These flame retardant aids can be used alone or in combination of two or more. Among these, antimony trioxide can be particularly preferably used.

【0017】配合量は、スチレン系樹脂100重量部に
対して、2〜10重量部とする。上記範囲外の添加量で
は難燃助剤の難燃性向上効果はみられない。本発明の難
燃樹脂組成物には、本発明の目的を損なわない範囲で他
の添加剤、例えば、滑剤、可塑剤、帯電防止剤、酸化防
止剤、紫外線吸収剤、充填剤、補強剤、顔料、着色剤等
を添加することができる。
The compounding amount is 2 to 10 parts by weight based on 100 parts by weight of the styrene resin. If the amount is outside the above range, the effect of improving the flame retardancy of the flame retardant auxiliary is not observed. In the flame-retardant resin composition of the present invention, other additives within a range that does not impair the purpose of the present invention, for example, a lubricant, a plasticizer, an antistatic agent, an antioxidant, an ultraviolet absorber, a filler, a reinforcing agent, Pigments, colorants and the like can be added.

【0018】なお、本発明の樹脂組成物のペレットは、
上記各成分をヘンシェルミキサー、二軸押出機等を用い
て溶融混練し、ペレタイザーにより製造することができ
る。本発明の樹脂組成物のペレットを射出成形等によ
り、テレビ、ビデオ再生機、ステレオ録音・再生機、ラ
ジオ、車搭載用ナビゲーター、電話機、携帯電話機、冷
蔵庫、空調機、掃除機、照明器具、コンピューター等の
電気又は電子機器製品用ハウジングが得られる。
The pellets of the resin composition of the present invention are:
The above components can be melt-kneaded using a Henschel mixer, a twin-screw extruder, or the like, and can be manufactured by a pelletizer. TV, video player, stereo recorder / player, radio, car-mounted navigator, telephone, mobile phone, refrigerator, air conditioner, vacuum cleaner, lighting fixture, computer Thus, a housing for an electric or electronic device product is obtained.

【0019】[0019]

【実施例】次に実施例及び比較例により本発明を説明す
る。 〔実施例1〜10、比較例1〜6〕第1表、及び第3表
にそれぞれ示した各成分をヘンシェルミキサーで混合
し、二軸押出機で溶融混練した後、ペレット化し、射出
成形により各種試験片を作成した。それらの試験片の評
価結果を第2表、及び第4に示す。
Next, the present invention will be described with reference to Examples and Comparative Examples. [Examples 1 to 10, Comparative Examples 1 to 6] The components shown in Tables 1 and 3 were mixed in a Henschel mixer, melt-kneaded in a twin-screw extruder, pelletized, and injection-molded. Various test pieces were prepared. The evaluation results of these test pieces are shown in Table 2 and 4.

【0020】組成物の成分として用いたものは以下の通
りである。 (1)樹脂 (a)ゴム変性スチレン系重合体 ・・・・・・・・・・(以下「PS」) (ハイインパクトポリスチレン,分子量200,000,ゴム含有量 8重量%,ゴム粒径2μm,IDEMITSU PS HT52) (2)繊維フイ ラ− (a)レ−ヨン繊維(繊維径50μm、日本火薬製ブル−RSで染色、1mm 長、ダイワ紡績製) (以下「繊維フィラ−1」) (b)レ−ヨン繊維(繊維径50μm、日本火薬製ブル−RSで染色、0.0 5mm長、ダイワ紡績製) (以下「繊維フィラ−2」) (c)レ−ヨン繊維(繊維径50μm、日本火薬製ブル−RSで染色、3mm 長、ダイワ紡績製) (以下「繊維フィラ−3」) (d)レ−ヨン繊維(繊維径 1μm、日本火薬製ブル−RSで染色、1mm 長、ダイワ紡績製) (以下「繊維フィラ−4」) (e)レ−ヨン繊維(繊維径150μm、日本火薬製ブル−RSで染色、1m m長、ダイワ紡績製) (以下「繊維フィラ−5」) (f)ポリエステル繊維(繊維径50μm、日本火薬製ブル−RSで染色、1 mm長、ユニチカ製) (以下「繊維フィラ−6」) (g)ポリエステル繊維(繊維径50μm、日本火薬製ブル−RSで染色、3 mm長、ユニチカ製) (以下「繊維フィラ−7」) (3)分散剤 (a)ステアリン酸亜鉛:日本油脂品 (以下「St−Zn」) (4)難燃剤 (a)臭素化ビスフェノ−ル型エポキシ重合体 (以下「難燃剤P」) (大日本インキ化学工業社製 EC−14) (b)ポリハロゲン化ジフェニルアルカン (以下「難燃剤Q」) (アルベマ−ル社製 Saytex8010) (c)臭素化トリアジン系難燃剤 (以下「難燃剤R」) (第一工業製薬社製 SR−245) (d)ポリメチルフェニルインデン系難燃剤 (以下「難燃剤S」) (DSB社製 FR−1808) (5)難燃助剤 (a)三酸化アンチモン (以下「Sb203」) 難燃性等の評価は、以下の方法で行った。 (1)難燃性 得られた試験片(寸法127mm×13mm×2.5m
m)をUL−94規格に準拠して評価した。 (2)一般物性 得られた試験片について、曲げ弾性率、アイゾット衝撃
値及び熱変形温度を、それぞれJIS K7203、K
7110及びK7207に準拠して測定した。 (3)ウエルド外観 第1、3表の組成物を射出成形により多点ゲ−トの箱型
形状のものを製作し樹脂の合流ウエルド部について良
好、不可の二段階で評価した。
The following were used as components of the composition. (1) Resin (a) Rubber-modified styrenic polymer (hereinafter “PS”) (high impact polystyrene, molecular weight 200,000, rubber content 8% by weight, rubber particle size 2 μm) , IDEMITSU PS HT52) (2) Fiber filler (a) Rayon fiber (fiber diameter 50 μm, dyed with Nippon Kayaku Bull-RS, 1 mm length, manufactured by Daiwa Spinning) (hereinafter “Fiber Filler-1”) ( b) Rayon fiber (fiber diameter 50 μm, dyed with Nippon Kayaku Bull-RS, 0.05 mm length, manufactured by Daiwa Spinning) (hereinafter “fiber filler-2”) (c) rayon fiber (fiber diameter 50 μm) Dyed with Nippon Kayaku Bull-RS, 3 mm length, manufactured by Daiwa Spinning Co., Ltd. (hereinafter, “Fiber Filler-3”) (d) Rayon fiber (fiber diameter: 1 μm, dyed with Nippon Kayaku Blue-RS, 1 mm length, Daiwa Spinning) Weifiller-4 ") (e) Rayon fiber (fiber diameter 150 µm, dyed with Nippon Kayaku Blue-RS, 1 mm long, manufactured by Daiwa Spinning) (hereinafter" fiber filler-5 ") (f) Polyester fiber ( Fiber diameter 50 μm, dyed with Nippon Kayaku Bull-RS, 1 mm length, made by Unitika Ltd. (hereinafter “fiber filler-6”) (g) Polyester fiber (fiber diameter 50 μm, dyed with Nippon Kayaku Blue-RS, 3 mm (Hereinafter, "Fiber Filler-7") (3) Dispersant (a) Zinc stearate: Nippon Oil & Fat (hereinafter "St-Zn") (4) Flame retardant (a) Brominated bisphenol Type epoxy polymer (hereinafter "flame retardant P") (EC-14 manufactured by Dainippon Ink and Chemicals, Inc.) (b) polyhalogenated diphenylalkane (hereinafter "flame retardant Q") (Saytex 8010 manufactured by Albemarle) (c) ) Bromination Triazine-based flame retardant (hereinafter “flame retardant R”) (Daiichi Kogyo Seiyaku Co., Ltd. SR-245) (d) Polymethylphenylindene-based flame retardant (hereinafter “flame retardant S”) (DSB FR-1808) ( 5) Flame retardant aid (a) Antimony trioxide (hereinafter "Sb203") Evaluation of flame retardancy and the like was performed by the following method. (1) Flame retardancy The obtained test piece (dimension 127 mm x 13 mm x 2.5 m
m) was evaluated in accordance with the UL-94 standard. (2) General physical properties The obtained test pieces were measured for flexural modulus, Izod impact value and heat deformation temperature according to JIS K7203 and K
It was measured according to 7110 and K7207. (3) Weld Appearance The compositions shown in Tables 1 and 3 were manufactured by injection molding into box-shaped multipoint gates, and the merging weld portion of the resin was evaluated in two levels of good and bad.

【0021】(〇:良好、×:不可と表示) (4)熱安定性評価 溶融混練樹脂組成物のペレットを射出成形機内に220
℃にて20分滞留させた後、40×110mmの板状の
成形品を成形しシルバ−の発生具合を目視にて良好、不
可の二段階で評価した。
(〇: good, ×: not good) (4) Evaluation of Thermal Stability A pellet of the melt-kneaded resin composition was placed in an injection molding machine for 220 minutes.
After holding at 20 ° C. for 20 minutes, a plate-like molded product of 40 × 110 mm was molded, and the degree of silver generation was visually evaluated in two stages of good and bad.

【0022】(〇:良好、×:不可と表示)(〇: good, ×: bad)

【0023】[0023]

【表1】 [Table 1]

【0024】[0024]

【表2】 [Table 2]

【0025】[0025]

【表3】 [Table 3]

【0026】[0026]

【表4】 [Table 4]

【0027】[0027]

【効果】本発明の樹脂組成物は、特定の有機繊維と分散
剤を用いることにより、成形品の外観及び成形時の熱安
定性に優れているため、特に電気、電子機器製品用ハウ
ジングに無塗装で好適に使用できる。さらに、難燃剤と
難燃助剤を特定量用いることにより、難燃性と他の諸物
性(衝撃強度、耐熱性等)のバランスにすぐれた成形品
が得られる。
The resin composition of the present invention is excellent in appearance and heat stability at the time of molding by using a specific organic fiber and a dispersant. Suitable for painting. Further, by using a specific amount of the flame retardant and the flame retardant auxiliary, a molded article having a good balance between flame retardancy and other physical properties (impact strength, heat resistance, etc.) can be obtained.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】(A)スチレン系樹脂100重量部に対し
て、(B)繊維径が5〜100ミクロンで繊維長が0.
01〜2mmの有機繊維0.1〜2重量部、及び(C)
分散剤0.1〜3重量部を配合してなるスチレン系樹脂
組成物。
1. A fiber having a fiber diameter of 5 to 100 microns and a fiber length of 0.1 to 100 parts by weight of a styrene resin (A).
0.1 to 2 parts by weight of organic fiber of 01 to 2 mm, and (C)
A styrenic resin composition containing 0.1 to 3 parts by weight of a dispersant.
【請求項2】(B)有機繊維がレ−ヨン系、ポリエステ
ル系又はナイロン系繊維である請求項1に記載のスチレ
ン系樹脂組成物。
2. The styrenic resin composition according to claim 1, wherein (B) the organic fiber is a rayon-based, polyester-based or nylon-based fiber.
【請求項3】(C)分散剤が高級脂肪酸又はその金属塩
である請求項1又は2に記載のスチレン系樹脂組成物。
3. The styrenic resin composition according to claim 1, wherein (C) the dispersant is a higher fatty acid or a metal salt thereof.
【請求項4】スチレン系樹脂100重量部に対して、さ
らに(D)難燃剤3〜30重量部、及び(E)難燃助剤
2〜10重量部を配合してなる請求項1〜3のいずれか
に記載のスチレン系樹脂組成物。
4. The composition according to claim 1, further comprising (D) 3 to 30 parts by weight of a flame retardant and (E) 2 to 10 parts by weight of a flame retardant aid per 100 parts by weight of the styrene resin. The styrenic resin composition according to any one of the above.
【請求項5】(D)難燃剤が臭素化ビスフェノ−ル型エ
ポキシ重合体、ポリハロゲン化ジフェニルアルカン、臭
素化トリアジン、ポリメチルフェニルインデン系難燃剤
のうちの少なくとも1種類である請求項4記載のスチレ
ン系樹脂組成物。
5. The flame retardant of claim 4, wherein the flame retardant is at least one of a brominated bisphenol type epoxy polymer, a polyhalogenated diphenylalkane, a brominated triazine, and a polymethylphenylindene flame retardant. Styrene resin composition.
【請求項6】請求項1〜5のいずれかに記載のスチレン
系樹脂組成物を成形してなる電気又は、電子機器製品用
ハウジング。
6. A housing for an electric or electronic device product obtained by molding the styrene resin composition according to claim 1.
JP22263397A 1997-08-19 1997-08-19 Styrene resin composition and electrical or electronic appliance housing made therefrom Pending JPH1160854A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22263397A JPH1160854A (en) 1997-08-19 1997-08-19 Styrene resin composition and electrical or electronic appliance housing made therefrom

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22263397A JPH1160854A (en) 1997-08-19 1997-08-19 Styrene resin composition and electrical or electronic appliance housing made therefrom

Publications (1)

Publication Number Publication Date
JPH1160854A true JPH1160854A (en) 1999-03-05

Family

ID=16785520

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22263397A Pending JPH1160854A (en) 1997-08-19 1997-08-19 Styrene resin composition and electrical or electronic appliance housing made therefrom

Country Status (1)

Country Link
JP (1) JPH1160854A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015217552A (en) * 2014-05-15 2015-12-07 東洋スチレン株式会社 Method for production of styrenic flame-retardant resin composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015217552A (en) * 2014-05-15 2015-12-07 東洋スチレン株式会社 Method for production of styrenic flame-retardant resin composition

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