JPS61252256A - Flame-retardant propylene polymer composition - Google Patents

Flame-retardant propylene polymer composition

Info

Publication number
JPS61252256A
JPS61252256A JP8612785A JP8612785A JPS61252256A JP S61252256 A JPS61252256 A JP S61252256A JP 8612785 A JP8612785 A JP 8612785A JP 8612785 A JP8612785 A JP 8612785A JP S61252256 A JPS61252256 A JP S61252256A
Authority
JP
Japan
Prior art keywords
flame
propylene
contg
polymer
weight
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
JP8612785A
Other languages
Japanese (ja)
Inventor
Tatsuo Kobayashi
辰男 小林
Kimiho Osegaki
小瀬垣 公穂
Satoru Hattori
悟 服部
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.)
Mitsubishi Petrochemical Co Ltd
Original Assignee
Mitsubishi 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 Mitsubishi Petrochemical Co Ltd filed Critical Mitsubishi Petrochemical Co Ltd
Priority to JP8612785A priority Critical patent/JPS61252256A/en
Publication of JPS61252256A publication Critical patent/JPS61252256A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide the titled compsn. which inhibits bleeding of flame retarder and gives moldings having excellent surface appearance, consisting of a propylene polymer, an acetyl group-contg. polymer, a halogen-contg. flame retarder and a flame-retardant aid. CONSTITUTION:100pts.wt. propylene polymer (A) such as propylene homopolymer or block, random or graft copolymer composed of a major proportion of propylene and a minor proportion of other copolymerizable monomers such as alpha-olefin, an unsaturated carboxylic acid (derivative) or an unsaturated organosilane, 3-50pts.wt. acetyl group-contg. polymer (B) such as ethylene/vinyl acetate copolymer having a vinyl acetate content of 10-90wt%, 1-100pts.wt. halogen-contg. flame retarder (C) [e.g. bis(2,3-dibromopropyl)ether of tetra bromobisphenol A], 0.5-50pts.wt. flame-retardant aid (D) (e.g. Sb2O3) and option ally, additives (E) such as reinforcing filler (e.g. carbon black), antioxidant, etc., are melt-kneaded.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、難燃剤のブリードが改善され、成形品表面外
観の良好なプロピレン重合体組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a propylene polymer composition with improved flame retardant bleed and a good surface appearance of molded articles.

(従来の技術) 成形性と機械的特性に優れるプロピレン重合体に難燃剤
を配して難燃化した材料は、種々の分野で広く用いられ
ている。
(Prior Art) A flame-retardant material made by adding a flame retardant to a propylene polymer, which has excellent moldability and mechanical properties, is widely used in various fields.

しかしながら、特にハロゲン系難燃剤を用いた組成物で
は、難燃剤が経時的にブリードして最終成形品の表面外
観を悪くする外、難燃性能も低下してしまう欠点を有す
る。
However, compositions using halogen flame retardants in particular have the drawback that the flame retardant bleeds over time, impairing the surface appearance of the final molded product and also reducing flame retardant performance.

(発明が解決しようとする問題点) 本発明は、従来技術の欠点、即ち、ハロゲン難燃剤のブ
リードを改善することを目的に、特定の重合体を併用す
ることによってこの目的が達成されることを見い出して
為された。
(Problems to be Solved by the Invention) The present invention aims to improve the drawbacks of the prior art, that is, the bleeding of halogen flame retardants, and aims to achieve this purpose by using a specific polymer in combination. He discovered and did it.

(問題点を解決するための手段) 即ち、本発明は、「プロピレン重合体100重量部、ア
セチル基含有重合体3〜50重量部、ハロゲン系難燃剤
1〜100重量部および難燃助剤0.5〜50重量部か
らなることを特徴とする難燃性プロピレン重合体組成物
」である。
(Means for Solving the Problems) That is, the present invention provides ``100 parts by weight of a propylene polymer, 3 to 50 parts by weight of an acetyl group-containing polymer, 1 to 100 parts by weight of a halogen flame retardant, and 0 parts by weight of a flame retardant aid. .5 to 50 parts by weight of a flame-retardant propylene polymer composition.

(作業) 本発明で用いるプロピレン重合体は、プロピレンの単独
重合体、過半重量のプロピレンと他のα−オレフィン(
エチレン、シラン、ヘキセン、4−メチルペンテン等)
、不飽和カルボン酸またはその誘導体、不飽和有機シラ
ン等共重合可能な単量体とのブロック、ランダム、グラ
フト共重合体である。結晶性のものが実用性に富んでい
て好ましい。
(Work) The propylene polymer used in the present invention is a homopolymer of propylene, a majority of the weight of propylene, and other α-olefins (
(ethylene, silane, hexene, 4-methylpentene, etc.)
, unsaturated carboxylic acids or their derivatives, unsaturated organic silanes, and other copolymerizable monomers, such as block, random, or graft copolymers. Crystalline materials are preferred because they are highly practical.

本発明で用いるアセチル基含有重合体は、例えば、ポリ
酢酸ビニル、エチレン−酢酸ビニル共重合体、これらの
部分ケン化物、酢酸ビニルグラフトポリオレフィン(ポ
リエチレン、ポリプロピレン等)などがある。このもの
の好ましいものとしては、酢酸ビニル含量が10〜90
重量%のエチレン−酢酸ビニル共重合体があ抄、特に好
ましくは、酢酸ビニル含量15〜70重量%のエチレン
−酢酸ビニル共重合体がある。これらの数値はブリード
改良効果の点で求められたものである。
Examples of the acetyl group-containing polymer used in the present invention include polyvinyl acetate, ethylene-vinyl acetate copolymer, partially saponified products thereof, and vinyl acetate graft polyolefin (polyethylene, polypropylene, etc.). This material preferably has a vinyl acetate content of 10 to 90.
Particularly preferred are ethylene-vinyl acetate copolymers having a vinyl acetate content of 15 to 70% by weight. These values were determined from the viewpoint of the bleeding improvement effect.

本発明で使用されるハロゲン系離燃剤は、例えば、テト
ラブロモビスフェノールAのビス(2,3−ジブロモプ
ロピル)エーテル、テトラブロモビスフェノールSのビ
ス(2,3−ジブロモプロピル)エーテル、テトラブロ
モビスフェノールA1デカブロモジフエニルオキサイド
、トリス(2,3−ジブロモプロピル)イソシアヌレー
ト、ペンタブロモトルエン、トリブロモプロパン、2.
2−ビス(4−ハイドロキシ−S、S−シー/コモ−フ
ェニル)プロパン等である。
Examples of the halogen-based flame retardants used in the present invention include bis(2,3-dibromopropyl) ether of tetrabromobisphenol A, bis(2,3-dibromopropyl) ether of tetrabromobisphenol S, and tetrabromobisphenol A1. Decabromodiphenyl oxide, tris(2,3-dibromopropyl)isocyanurate, pentabromotoluene, tribromopropane, 2.
2-bis(4-hydroxy-S,S-C/como-phenyl)propane and the like.

本発明で使用される難燃助剤としては、無機化合物が良
く、例えば、三酸化アンチモン、四酸化アンチモン、五
酸化アンチモン、ピロアンチモン酸ソーダ、二酸化スズ
、メタホウ酸バリウム、ホウ酸亜鉛、酸化ジルコニウム
、酸化モリブデン等を挙げることができる。
The flame retardant aid used in the present invention is preferably an inorganic compound, such as antimony trioxide, antimony tetroxide, antimony pentoxide, sodium pyroantimonate, tin dioxide, barium metaborate, zinc borate, zirconium oxide. , molybdenum oxide, and the like.

これらの各必須成分の配合割合は、プロピレン重合体i
oo重量部に対して、アセチル基含有重合体3〜50重
量部、好ましくは5〜30ii量部、上記難燃剤1〜1
00重量部、好ましくは2〜50重量部および難燃助剤
0゜5〜50重量部、好ましくは1〜25重量部である
。アセチル基含有重合体と難燃助剤の量は、それぞれ上
記難燃剤の3分の1以上であることが効果の点でより好
ましい。
The blending ratio of each of these essential components is as follows: propylene polymer i
3 to 50 parts by weight of the acetyl group-containing polymer, preferably 5 to 30 parts by weight, and 1 to 1 parts by weight of the above flame retardant per oo parts by weight.
0.00 parts by weight, preferably 2 to 50 parts by weight and flame retardant aids 0.5 to 50 parts by weight, preferably 1 to 25 parts by weight. From the viewpoint of effectiveness, it is more preferable that the amounts of the acetyl group-containing polymer and the flame retardant aid are each one-third or more of the flame retardant.

アセチル基含有重合体の量が3重量部未満ではブリード
改良効果が発現せず、一方、50重量部を越えると物性
が低下する。
If the amount of the acetyl group-containing polymer is less than 3 parts by weight, the bleeding improvement effect will not be exhibited, while if it exceeds 50 parts by weight, the physical properties will deteriorate.

上記難燃剤の量が1重量部未満では難燃性が劣り、一方
、ioo重量部を越えると助成物の強度が低下する上、
経済的にも問題である。
If the amount of the flame retardant is less than 1 part by weight, the flame retardancy will be poor, while if it exceeds 100 parts by weight, the strength of the supplement will decrease,
It is also an economic problem.

難燃助剤の量が0.5重量部未満では難燃剤との相乗作
用が小さく、一方、50重量部を越えると物性が低下し
、且つ、経済的にも実用的でない。
If the amount of the flame retardant aid is less than 0.5 parts by weight, the synergistic effect with the flame retardant will be small, while if it exceeds 50 parts by weight, the physical properties will deteriorate and it is not economically practical.

本発明組成物には、これら必須成分の外に付加的成分を
本発明の効果を著しく損なわない範囲で配合することが
できる。例えば、強化充填材として、タルク、マイカ、
炭酸カルシウム、シリカ、ガラス繊維等を添加すること
ができる。その外、老化防止剤、加工時安定剤、造核剤
、滑剤、紫外線吸収剤、帯電防止剤、離型剤、発泡剤、
顔料、分散剤等も必要に応じて添加することができる。
In addition to these essential components, the composition of the present invention may contain additional components within a range that does not significantly impair the effects of the present invention. For example, talc, mica,
Calcium carbonate, silica, glass fiber, etc. can be added. In addition, anti-aging agents, processing stabilizers, nucleating agents, lubricants, ultraviolet absorbers, antistatic agents, mold release agents, foaming agents,
Pigments, dispersants, etc. can also be added as necessary.

本発明の組成物の製造方法は、一般のプロピレン重合体
と同様に所要成分の所定量の混合物をバンバリーミキサ
−、ニーター、ロールミル、スクリュ一式単軸押出機、
二軸押出機等によって溶融混練して得られるが、場合に
よっては、各成分の混合物を直接、射出、圧縮、フィル
ム等の成形機に投入して成形品として得られる。
The method for producing the composition of the present invention is to mix a predetermined amount of the required components in a Banbury mixer, kneader, roll mill, single screw extruder, etc., as in the case of general propylene polymers.
It is obtained by melt-kneading using a twin-screw extruder or the like, but in some cases, a molded product can be obtained by directly putting the mixture of each component into a molding machine such as an injection, compression, or film molding machine.

(実施例) 以下に示す例の中で、燃焼性の測定は、UL規格UL9
4に定められた方法に基づいて実施した。
(Example) In the examples shown below, the measurement of flammability is based on UL standard UL9.
It was carried out based on the method specified in 4.

ブリード性については、射出成形シートを用いて次式で
求められるシート表面の光沢差および目視判定により評
価した。光沢差が小さい橿ブリード性は良好である。
Bleedability was evaluated using an injection molded sheet by the difference in gloss on the sheet surface determined by the following formula and by visual judgment. The gloss bleed property is good with a small difference in gloss.

光沢差=〔オーブンテスト前の光沢)−(70℃オーブ
ンで7日間放置後の光沢〕 目視判定基単 ブリードが非常に多い ;× ブリードが多い    ;Δ ブリードが少ない   ;ロ ブリードが非常に少ない;○ ブリードがない     t◎ 実施例1〜3および比較例1〜3 メルト70−レート8のプロピレンホモポリマーを用い
て、第1表に示す配合で調整した組成物を、森山製作所
製加圧双腕ニーダ−を用いて200℃にて混練し、更に
ペレタイザーを用いてベレント化した。
Gloss difference = [Gloss before oven test] - (Gloss after being left in a 70℃ oven for 7 days) Visual judgment: Very much single bleed; × Much bleed; Δ Little bleed; Very little lobed; ○ No bleed t◎ Examples 1 to 3 and Comparative Examples 1 to 3 Using a propylene homopolymer with a melt of 70 and a rate of 8, a composition prepared according to the formulation shown in Table 1 was heated in a pressurized double-arm kneader manufactured by Moriyama Seisakusho. The mixture was kneaded at 200°C using -, and then made into a pellet using a pelletizer.

然る後、これを東芝機械社製射出成形機(IS90B型
)を用いて80閣×120譚×2鱈のシート試験片及び
UL94に定める燃焼性試験片を成形し、ブリード性及
び燃焼性を評価した。
After that, this was molded into 80 x 120 x 2 cod sheet test pieces and flammability test pieces specified by UL94 using an injection molding machine manufactured by Toshiba Machine Co., Ltd. (IS90B model), and the bleedability and combustibility were evaluated. evaluated.

実施例4〜9および比較例4〜8 メルトフローレート30のエチレン−プロピレンブロッ
ク共重合体(エチレン含!6重量%)又はメルトフロー
レイト8のプロピレンホモポリマーを用いて、第1表に
示す配合で調整した組成物をヘンシェルミキサーで十分
混合した後、スクリュ一式二軸押出機にて溶融押出し、
ペレタイザーを用いてペレット化した。
Examples 4 to 9 and Comparative Examples 4 to 8 Using an ethylene-propylene block copolymer (containing 6% by weight of ethylene) with a melt flow rate of 30 or a propylene homopolymer with a melt flow rate of 8, the formulations shown in Table 1 were prepared. After thoroughly mixing the composition prepared in a Henschel mixer, it was melt-extruded using a twin-screw extruder,
Pelletized using a pelletizer.

これを用いて実施例1と同様にして評価した。Evaluation was performed in the same manner as in Example 1 using this.

C以下余白)Margin below C)

Claims (1)

【特許請求の範囲】[Claims] プロピレン重合体100重量部、アセチル基含有重合体
3〜50重量部、ハロゲン系難燃剤1〜100重量部お
よび難燃助剤0.5〜50重量部からなることを特徴と
する難燃性プロピレン重合体組成物。
Flame-retardant propylene comprising 100 parts by weight of a propylene polymer, 3 to 50 parts by weight of an acetyl group-containing polymer, 1 to 100 parts by weight of a halogen flame retardant, and 0.5 to 50 parts by weight of a flame retardant aid. Polymer composition.
JP8612785A 1985-04-22 1985-04-22 Flame-retardant propylene polymer composition Pending JPS61252256A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8612785A JPS61252256A (en) 1985-04-22 1985-04-22 Flame-retardant propylene polymer composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8612785A JPS61252256A (en) 1985-04-22 1985-04-22 Flame-retardant propylene polymer composition

Publications (1)

Publication Number Publication Date
JPS61252256A true JPS61252256A (en) 1986-11-10

Family

ID=13878039

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8612785A Pending JPS61252256A (en) 1985-04-22 1985-04-22 Flame-retardant propylene polymer composition

Country Status (1)

Country Link
JP (1) JPS61252256A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63146949A (en) * 1986-12-10 1988-06-18 Mitsubishi Petrochem Co Ltd Flame-retardant polyolefin composition
US5216059A (en) * 1992-04-13 1993-06-01 Great Lakes Chemical Corp. Flame retardant additive composition useful with polyolefins
JP2012025792A (en) * 2010-07-20 2012-02-09 Yazaki Corp Flame-retardant olefinic resin composition and flame-retardant tape

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52127955A (en) * 1976-04-19 1977-10-27 Nissan Chem Ind Ltd Flame-retardant polyolefin resin compositions
JPS61215639A (en) * 1985-03-22 1986-09-25 Tokuyama Soda Co Ltd Flame-retardant resin composition
JPS61221248A (en) * 1985-03-28 1986-10-01 Tokuyama Soda Co Ltd Flame-retardant resin composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52127955A (en) * 1976-04-19 1977-10-27 Nissan Chem Ind Ltd Flame-retardant polyolefin resin compositions
JPS61215639A (en) * 1985-03-22 1986-09-25 Tokuyama Soda Co Ltd Flame-retardant resin composition
JPS61221248A (en) * 1985-03-28 1986-10-01 Tokuyama Soda Co Ltd Flame-retardant resin composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63146949A (en) * 1986-12-10 1988-06-18 Mitsubishi Petrochem Co Ltd Flame-retardant polyolefin composition
US5216059A (en) * 1992-04-13 1993-06-01 Great Lakes Chemical Corp. Flame retardant additive composition useful with polyolefins
JP2012025792A (en) * 2010-07-20 2012-02-09 Yazaki Corp Flame-retardant olefinic resin composition and flame-retardant tape

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