JPS61174263A - Flame-retardant thermoplastic synthtic resin composition for molding film - Google Patents

Flame-retardant thermoplastic synthtic resin composition for molding film

Info

Publication number
JPS61174263A
JPS61174263A JP1386085A JP1386085A JPS61174263A JP S61174263 A JPS61174263 A JP S61174263A JP 1386085 A JP1386085 A JP 1386085A JP 1386085 A JP1386085 A JP 1386085A JP S61174263 A JPS61174263 A JP S61174263A
Authority
JP
Japan
Prior art keywords
film
weight
synthetic resin
fiber
inorg
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
JP1386085A
Other languages
Japanese (ja)
Other versions
JPH0250141B2 (en
Inventor
Takashi Mineo
峯尾 敬
Makoto Ozawa
誠 小沢
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.)
Nitto Boseki Co Ltd
Original Assignee
Nitto Boseki 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 Nitto Boseki Co Ltd filed Critical Nitto Boseki Co Ltd
Priority to JP1386085A priority Critical patent/JPS61174263A/en
Publication of JPS61174263A publication Critical patent/JPS61174263A/en
Publication of JPH0250141B2 publication Critical patent/JPH0250141B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled compsn. which has excellent flame retardance, toughness and film-moldability and gives a film having excellent surface smoothness and suitable for use in the surface decoration of incombustible, sound absorbing interior finish materials, by blending a thermoplastic synthetic resin with an inorg. filler. CONSTITUTION:A 30-60wt% thermoplastic synthetic resin (A) (e.g. PP or PS) having a glass transition temp. of 50-120 deg.C and contg. no halogen, 40-70wt% inorg. filler (B) composed of 5.2-43pts.wt. colloidal inorg. fiber (e.g. potassium titanate fiber) having a fiber diameter of 3mu or below, a fiber length of 30mu or below and an aspect ratio of 10 per 100pts.wt. inorg. powder [e.g. Al(OH)3 or Mg(OH)2] having a particle size of 40mu or below, which is dehydrated by heating, and additives (C) such as thermal stabilizer, ultraviolet light stabilizer, plasticizer, lubricant, antistatic agent, thickener, dispersant, etc., are kneaded with heating in an extruder.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は高度な難燃性とタフネス、およびカレンダー成
型性にすぐれたフィルム成型用難燃性熱可塑性合成樹脂
組成物に関するものであって、得られたフィルムは主と
して不燃性、断熱性、吸音性、内装材の表面化粧用フィ
ルムとして使用する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a flame-retardant thermoplastic synthetic resin composition for film molding that has a high degree of flame retardancy, toughness, and excellent calendar moldability. The obtained film is mainly used as a nonflammable, heat-insulating, sound-absorbing film, and as a decorative surface film for interior materials.

〔従来の技術〕[Conventional technology]

従来合成樹脂の難燃化技術としては、合成樹脂原料に対
して、ハロゲン化合物、含燐化合物、含窒素化合物、酸
化アンチモン等の難燃化剤を配合する方法が用いられて
いるが、このような難燃化剤は比較的高価であるうえ、
成型時や高温にさらされたときに有害なガスを発生する
危険がある。
Conventional flame retardant technology for synthetic resins involves adding flame retardants such as halogen compounds, phosphorus compounds, nitrogen compounds, and antimony oxide to synthetic resin raw materials. Flame retardants are relatively expensive, and
There is a risk of generating harmful gases during molding or when exposed to high temperatures.

近年このような危険性のない無機質の充填材を、合成樹
脂中に充填して難燃化を計る試みがなされているが、無
機質充填材のみを使用して難燃化を計る場合、樹脂中に
多量に配合することが必要となり、フィルムの成型性を
低下し、フィルムの強度を劣化する。
In recent years, attempts have been made to make flame retardant by filling synthetic resin with non-hazardous inorganic fillers. It is necessary to incorporate a large amount of the film into the film, which reduces the moldability of the film and deteriorates the strength of the film.

この改良のため、前記難燃化剤と無機質の充填材を併用
し、無機質充填材の配合量を低減する試みがなされてい
るが、充分な難燃効果が得られ難いばかりでなく、熱可
塑性合成樹脂に併用する無機質充填材の量もそれ程減少
させることができないため、フィルムの成型性を低下し
、フィルムの強度を劣化する。
In order to improve this, attempts have been made to reduce the amount of inorganic filler by using the flame retardant and inorganic filler together, but not only is it difficult to obtain a sufficient flame retardant effect, but also thermoplastic Since the amount of inorganic filler used in combination with the synthetic resin cannot be reduced to that extent, the moldability of the film is reduced and the strength of the film is deteriorated.

この改良のため、前記難燃化剤と無機質の充填材を併用
し、無機質充填材の配合量を低減する試みもなされてい
るが、効果が充分発揮できない許りか、成型性の向上に
直接結びつかない。
In order to improve this, attempts have been made to reduce the amount of inorganic filler by using the flame retardant and inorganic filler together, but the effect may not be sufficiently demonstrated or it may not directly lead to improved moldability. do not have.

一方フイルムの成型性を改良するため、比較的低分子量
の合成樹脂を配゛合することがあるが、低分子量の合成
樹脂は軟化点が低いためタフネスは低下する。又、ステ
アリン酸アルミニウム、金属石鹸など各種の滑剤、可塑
剤を配合することもあるが、難燃性、タフィ・スを含め
本質的な改善となっていない。
On the other hand, in order to improve the moldability of the film, a synthetic resin with a relatively low molecular weight is sometimes incorporated, but the low molecular weight synthetic resin has a low softening point, so the toughness is reduced. In addition, various lubricants and plasticizers such as aluminum stearate and metal soap are sometimes added, but these do not substantially improve flame retardancy or toffee properties.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

この発明は従来の合成樹脂の難燃化によって解決するこ
とのできなかった、成型時や高温にさらされた時にみら
れる有害なガスの発生、難燃化によって起される成型性
の低下、フィルムの強度。
This invention solves problems that could not be solved by making conventional synthetic resins flame retardant, such as the generation of harmful gases that occur during molding or when exposed to high temperatures, and the deterioration of moldability caused by flame retardation. strength of.

タフネスの劣下などのない高度の難燃性とタフィ・ス及
び成型性を有する合成樹脂組成物を得ることを目的とし
てし)る。
(Objective of the present invention is to obtain a synthetic resin composition having high flame retardancy, toughness, and moldability without deterioration in toughness.)

〔問題点を解決するための手段〕[Means for solving problems]

ガラス転移温度が50〜120℃で/’tロゲンを含ま
ない熱可塑性合成樹脂30〜60重量%と、加熱脱水型
無機質粉末100重量部に対しコロイド状無機繊維52
〜43重量部を含む無機質充填剤40〜70重量%とを
配合した組成物を得ることにより解決した。
30 to 60% by weight of a thermoplastic synthetic resin having a glass transition temperature of 50 to 120°C and containing no rogens, and 52 parts by weight of colloidal inorganic fiber to 100 parts by weight of heat-dehydrated inorganic powder.
The problem was solved by obtaining a composition containing 40-70% by weight of an inorganic filler containing ~43 parts by weight.

〔作 用〕[For production]

この発明の組成物は、ガラス転移温度が50〜120’
Cで、ハロゲンを含まない熱可塑性合成樹脂に対し、加
熱脱水型無機質粉末とコロイド状無機繊維とからなる無
機質充填材を配合したものであるから、組成物形成のた
めの混練時、或いはフィルム形成のための成型時、加熱
脱水型無機質粉末から発生する水蒸気はコロイド状無機
繊維間隙を通って揮散し、コロイド状無機繊維による補
強効果も加って、表面平滑性、タフネスの向上、更に加
熱脱水型無機質粉末とコロイド状無機繊維とからなる無
機質充填材のすぐれた難燃性を併せ有するものである。
The composition of this invention has a glass transition temperature of 50 to 120'.
In C, an inorganic filler consisting of a heat-dehydrated inorganic powder and a colloidal inorganic fiber is blended with a halogen-free thermoplastic synthetic resin, so it can be used during kneading for composition formation or film formation. During molding, the water vapor generated from the heat-dehydrated inorganic powder evaporates through the gaps between the colloidal inorganic fibers, and with the added reinforcing effect of the colloidal inorganic fibers, the surface smoothness and toughness are improved, and the heat-dehydrated inorganic powder is It combines the excellent flame retardancy of an inorganic filler made of molded inorganic powder and colloidal inorganic fibers.

〔実施例〕〔Example〕

本発明の組成物は、ガラス転移温度が50〜120℃で
、ハロゲンを含まない熱可塑性合成樹脂30〜60重量
%と、加熱脱水型無機質粉末100重量部に対し、コロ
イド状無機繊維5.2〜43重量部を含む無機質充填材
40〜70重量%とを配合してなるものであるが、ここ
に使用されるガラス転移温度が50〜120℃で、ハロ
ゲンを含まない熱可塑性合成樹脂としては、例えば、ポ
リエチレン、ポリプロピレン、ポリスチレン。
The composition of the present invention has a glass transition temperature of 50 to 120°C, 30 to 60% by weight of a halogen-free thermoplastic synthetic resin, and 5.2 parts by weight of colloidal inorganic fibers per 100 parts by weight of heat-dehydrated inorganic powder. It is made by blending 40 to 70% by weight of an inorganic filler containing ~43 parts by weight, and the glass transition temperature used here is 50 to 120°C, and as a halogen-free thermoplastic synthetic resin. , for example polyethylene, polypropylene, polystyrene.

ポリメタクリル酸エステル、ポリカーボネート。Polymethacrylic acid ester, polycarbonate.

ポリエチレンテレフタレート及びこれらの共重合体が有
利に使用され、加熱脱水型無機質粉末としては粒径が4
0μ以下の水酸化アルミニウム、水酸化マグネシウム、
水和硫酸カルシウム若しくはこれらの混合物が使用され
、難燃性、成型性を阻害しない範囲で、タルク、クレー
、炭酸カルシウム等で一部代替えしても差支えない。
Polyethylene terephthalate and copolymers thereof are advantageously used, and the heat-dehydrated inorganic powder has a particle size of 4.
0 μ or less aluminum hydroxide, magnesium hydroxide,
Hydrated calcium sulfate or a mixture thereof is used, and talc, clay, calcium carbonate, etc. may be partially substituted as long as flame retardancy and moldability are not impaired.

更にコロイド状無機繊維としては、チタン酸力り繊維、
窒化硼素繊維、メタ硅酸カルシウム(ワラストナイト)
、セピオライト、ヘッドマン繊維等で、繊維径3μ以下
、繊維長30μ以下でアスペクト比10程度のものを使
用する。
Furthermore, as colloidal inorganic fibers, titanic acid strained fibers,
Boron nitride fiber, calcium metasilicate (wollastonite)
, sepiolite, Hedman fiber, etc., with a fiber diameter of 3 μm or less, a fiber length of 30 μm or less, and an aspect ratio of about 10.

然して本発明の組成物は、前記加熱脱水型無機質粉末1
00重量部に対し、コロイド状無機繊維52〜43重量
部を混合した無機質充填材40〜70重量%と、ガラス
転移温度が50〜120°Cでハロゲンを含まない熱可
塑性合成樹脂30〜60重量%とを、加圧ロール、ニー
ダ−2押出゛機等を用い加熱混練法により混和して得る
ことができ、更に得られた組成物から、目的とするフィ
ルムを得るためには、押出機を用いて一旦予備成型した
後、カレンダーロール等によりフィルム状に圧延成型す
る。
Therefore, the composition of the present invention has the above-mentioned heat-dehydrated inorganic powder 1.
00 parts by weight, 40 to 70 parts by weight of an inorganic filler mixed with 52 to 43 parts by weight of colloidal inorganic fibers, and 30 to 60 parts by weight of a halogen-free thermoplastic synthetic resin with a glass transition temperature of 50 to 120°C. % by a heating kneading method using a pressure roll, a kneader-2 extruder, etc., and further, in order to obtain the desired film from the obtained composition, an extruder is used. After the film is preformed, it is rolled and formed into a film using a calendar roll or the like.

なお、本発明の組成物中には、組成物に要求される特性
を阻害しない範囲で、公知の熱安定剤。
In addition, the composition of the present invention may contain a known heat stabilizer to the extent that it does not impede the properties required of the composition.

紫外線安定剤、可塑剤、滑剤、帯電防止剤、増粘剤1分
散剤等を適宜添加配合しても良い。
Ultraviolet stabilizers, plasticizers, lubricants, antistatic agents, thickeners, dispersants, etc. may be added and blended as appropriate.

次に各種配合の本発明組成物から得られたフィルムにつ
いて難燃性を知るための燃焼性、引張り強さ、伸び、t
2.型性、平滑性を測定した結果を第1表に示す。
Next, in order to know the flame retardance of films obtained from the compositions of the present invention with various formulations, flammability, tensile strength, elongation, t
2. Table 1 shows the results of measuring moldability and smoothness.

熱可塑性合成樹脂は、密度0.865.エチレン含量1
2%の結fA性ポリプロピレンエチレン共重合体を用い
たが、組成4においては密度0945の高密度ポリエチ
レンを使用した。
The thermoplastic synthetic resin has a density of 0.865. Ethylene content 1
A 2% fA binding polypropylene ethylene copolymer was used, but in Composition 4, high density polyethylene with a density of 0945 was used.

無機質充填材の一成分である加熱脱水型無機粉末として
は平均粒径30μの水酸化アルミニウム〔商品名ハイシ
ライト、昭和電工株式会社製〕を用いた。但し実施例2
−4..5−5では、平均粒径30μの炭酸カルシウム
を使用した。無機質充填材の他方の成分であるコロイド
状無機繊維は繊維径3μ以下、繊維長30μ以下で、ア
スペクト比10のコロイド状チタン酸カリ繊維〔商品名
テイスモ、大塚化学株式会社製〕を用い、実施例5−5
では平均繊維径5 p 、平均繊維長100μのガラス
繊維粉を使用した。各組成物は加圧ニーグーで加熱混練
して製造し組成物を得た。
As the heat-dehydrated inorganic powder which is one component of the inorganic filler, aluminum hydroxide (trade name: Hisilite, manufactured by Showa Denko K.K.) with an average particle size of 30 μm was used. However, Example 2
-4. .. In 5-5, calcium carbonate with an average particle size of 30 μm was used. The colloidal inorganic fiber, which is the other component of the inorganic filler, has a fiber diameter of 3μ or less, a fiber length of 30μ or less, and a colloidal potassium titanate fiber [trade name Teismo, manufactured by Otsuka Chemical Co., Ltd.] with an aspect ratio of 10. Example 5-5
In this case, glass fiber powder having an average fiber diameter of 5 p and an average fiber length of 100 μm was used. Each composition was manufactured by heating and kneading in a pressurized niegu to obtain a composition.

難燃性を試験するための燃焼性の測定、およびり1張り
強さを測定するための試料は、平プレス機に前記組成物
を置き、スペーサーを用いて160℃で5分間加熱加圧
し、厚さ0.1 m、のフィルムを作り、適宜サイズに
裁断したものをそれぞれの試料につき5枚ずつ用意した
For the measurement of combustibility for testing flame retardancy and for measuring tensile strength, the composition was placed on a flat press machine, heated and pressurized at 160 ° C. for 5 minutes using a spacer, A film with a thickness of 0.1 m was made and cut into appropriate sizes, and five sheets were prepared for each sample.

燃焼性の測定は運輸省1車輌用材:′:i燃焼試験規格
FMVSS−302 J に準拠する、水平着火式のフ
レーム法で行い、フレーム開口部中央の試料に着火して
から火の消えるまでの時間を1試料につき5回測定し、
5回分の時間を加算してその合計秒数を表示した。
Flammability was measured using the horizontal ignition flame method, which complies with the Ministry of Transport's 1 Vehicle Materials: ':i Combustion Test Standard FMVSS-302J. The time was measured 5 times per sample,
The times for the five times were added up and the total number of seconds was displayed.

引張強さは前記と同様にして成型された厚さ0、1 m
mのフィルムを15mm巾に裁断して引張試験を行ない
、15m、巾での破断強度および破断時伸長度で表示し
た。
The tensile strength is 0.1 m thick molded in the same manner as above.
The film was cut into 15 mm widths and subjected to a tensile test, and the results were expressed as breaking strength and elongation at break at 15 mm width.

成型性の確認は押出機による予備成形装置付のカレンダ
ーロール成型機を用い0.1 mm厚のフィルムを作る
時の成型適性と成型後のフィルムの平滑性で判定し、下
記の記号区分により表示した。
Confirmation of moldability is determined by the moldability when making a 0.1 mm thick film using a calendar roll molding machine equipped with an extruder preforming device and the smoothness of the film after molding, and is indicated by the following symbol categories. did.

成型性  ◎容易に成型できるもの O成型適性があるもの △外観を問わず連続的にシート化が 可能なもの ×成型不可能なもの 平滑性  ◎きわめて平滑なもの ○フィッシュアイが少量あるが使用 上問題がないもの △ピンホール、フィッシュアイがあ り、地相不良のみられるもの ×穴、こぶ等があり使用にたえない もの この表から明らかな通り、熱可塑性合成樹脂に対し無機
質充填材として加熱脱水型無機質粉末のみを混合したも
のは、混合比率が大きくなればなる程、燃焼性が低下し
て難燃性が向上するが、破断強度、破断伸長度が低下し
、フィルム成型性。
Moldability ◎Things that can be easily molded △Things that are suitable for molding △Things that can be made into sheets continuously regardless of appearance Items with no problems △ Items with pinholes, fish eyes, and poor topography × Items with holes, bumps, etc. that are unusable When mixing only dehydrated inorganic powder, the higher the mixing ratio, the lower the flammability and the higher the flame retardancy, but the lower the breaking strength and the lower the elongation at break, and the lower the film formability.

フィルム平滑性共に急速に悪化することが理解される〇 これに対し本発明のように、熱可塑性合成樹脂30〜6
0重量%に対し、加熱脱水型無機質粉末とコロイド状無
機繊維からなる無機充填材を40〜70重量%混合した
ものは、無機質充填材の量が増加する程燃焼性が低下し
て難燃性が向上し、破断強度が微増し、破断伸長度は低
下するが、フィルム成型性、フィルム平滑性、は共に問
題がな−<、然も無機充填材中におけるコロイド状無機
繊維の量が多い程、燃焼性の低下即ち難燃性の向上と破
断強度の向上を認めることができる。
It is understood that both film smoothness deteriorates rapidly. In contrast, as in the present invention, thermoplastic synthetic resin 30 to 6
Compared to 0% by weight, a mixture of 40 to 70% by weight of an inorganic filler consisting of heat-dehydrated inorganic powder and colloidal inorganic fibers becomes flame retardant as the flammability decreases as the amount of inorganic filler increases. Although the strength at break increases slightly and the elongation at break decreases, there are no problems with both film formability and film smoothness. , a decrease in flammability, that is, an improvement in flame retardancy and an improvement in breaking strength can be observed.

そして無機質充填材の量が40重M%未満となると難燃
性に問題を生じ、70重量系を超えるとフィルムの破断
強度が低下し、フィルム成型性。
If the amount of inorganic filler is less than 40% by weight, problems will arise in flame retardancy, and if it exceeds 70% by weight, the breaking strength of the film will decrease, resulting in poor film formability.

平滑性も悪化する。又加熱脱水型無機粉末100重量部
に対゛しコロイド状無機繊維の量が52重量部未満のと
きはコロイド状無機繊維の添加による効果が認められず
、43重量部を超えるとフィルムの成型性、平滑性が悪
化する。
Smoothness also deteriorates. Furthermore, when the amount of colloidal inorganic fiber is less than 52 parts by weight based on 100 parts by weight of heat-dehydrated inorganic powder, no effect is observed due to the addition of colloidal inorganic fiber, and when it exceeds 43 parts by weight, the moldability of the film deteriorates. , the smoothness deteriorates.

〔発明の効果〕〔Effect of the invention〕

以上詳細に述べた通り、ガラス転移温度が50〜120
°Cで、ハロゲンを含まない熱可塑性合成樹脂30〜6
0重量%と、加熱脱水型無機粉末100重量部に対し、
コロイド状無機繊維5.2〜43重量部を含む無機質充
填材40〜70重量%とを配合した本発明の組成物は、
フィルム成型性特にカレンダー成型によるフィルム成型
性に富み、得られたフィルムは表面平滑性にすぐれ、然
も難燃性で有害ガスを発生することもなく、又、無機質
充填材、特に加熱脱水型無機粉末とコロイド状無機繊維
との併用により、フィルムの強度やタフネスの低下のな
いフィルムを形成し、不燃性、断熱性、吸音性の内装材
の表面化粧用フィルムとして顕著な効果を発揮するもの
である。
As described in detail above, the glass transition temperature is 50 to 120.
Halogen-free thermoplastic synthetic resin 30-6 °C
0% by weight and 100 parts by weight of heat-dehydrated inorganic powder,
The composition of the present invention contains 40 to 70% by weight of an inorganic filler containing 5.2 to 43 parts by weight of colloidal inorganic fibers,
The film has excellent film formability, especially by calendar molding, and the resulting film has excellent surface smoothness, is flame retardant, does not emit harmful gases, and is suitable for use with inorganic fillers, especially heat-dehydrated inorganic fillers. The combination of powder and colloidal inorganic fiber forms a film that does not reduce its strength or toughness, and exhibits remarkable effects as a surface decorative film for interior materials that are nonflammable, heat insulating, and sound absorbing. be.

特許出願人  日東紡績株式会社 代理人 弁理士  大 野 克 射 入  野  令  子 〃      大 野 柳之輔Patent applicant: Nittobo Co., Ltd. Agent: Patent Attorney Katsu Ohno Reiko Irino Yanosuke Ohno

Claims (1)

【特許請求の範囲】[Claims]  ガラス転移温度が50〜120℃で、ハロゲンを含ま
ない熱可塑性合成樹脂30〜60重量%と、加熱脱水型
無機粉末100重量部に対し、コロイド状無機繊維5.
2〜43重量部を含む無機質充填材40〜70重量%と
を配合した、フィルム成型用難燃性熱可塑性合成樹脂組
成物。
5.5% by weight of colloidal inorganic fiber based on 30% to 60% by weight of a thermoplastic synthetic resin having a glass transition temperature of 50 to 120°C and containing no halogen, and 100 parts by weight of heat-dehydrated inorganic powder.
A flame-retardant thermoplastic synthetic resin composition for film molding, which is blended with 40-70% by weight of an inorganic filler containing 2-43 parts by weight.
JP1386085A 1985-01-28 1985-01-28 Flame-retardant thermoplastic synthtic resin composition for molding film Granted JPS61174263A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1386085A JPS61174263A (en) 1985-01-28 1985-01-28 Flame-retardant thermoplastic synthtic resin composition for molding film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1386085A JPS61174263A (en) 1985-01-28 1985-01-28 Flame-retardant thermoplastic synthtic resin composition for molding film

Publications (2)

Publication Number Publication Date
JPS61174263A true JPS61174263A (en) 1986-08-05
JPH0250141B2 JPH0250141B2 (en) 1990-11-01

Family

ID=11845014

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1386085A Granted JPS61174263A (en) 1985-01-28 1985-01-28 Flame-retardant thermoplastic synthtic resin composition for molding film

Country Status (1)

Country Link
JP (1) JPS61174263A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0414110A2 (en) * 1989-08-21 1991-02-27 The B.F. Goodrich Company Compression molded flame retardant and high impact strength ultra high molecular weight polyethylene composition
JPH05320409A (en) * 1992-05-25 1993-12-03 Matsushita Electric Works Ltd Resinous molding material
JP2010085818A (en) * 2008-10-01 2010-04-15 Inoac Corp Sound absorbing material
CN106739225A (en) * 2016-12-06 2017-05-31 太仓大唐化纤厂 A kind of flame-retardant and anti-static sound insulation composite fiber plate and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52145453A (en) * 1976-05-28 1977-12-03 Nippon Steel Chem Co Ltd Fire-resistant composition
JPS5674137A (en) * 1979-11-21 1981-06-19 Kyowa Chem Ind Co Ltd Flame-retardant resin composition with improved mechanical strength and agent therefor
JPS56127643A (en) * 1980-03-10 1981-10-06 Showa Electric Wire & Cable Co Ltd Flame-retardant polyolefin composition
JPS596250A (en) * 1982-07-02 1984-01-13 Mitsubishi Rayon Co Ltd Resin composition having excellent surface smoothness

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52145453A (en) * 1976-05-28 1977-12-03 Nippon Steel Chem Co Ltd Fire-resistant composition
JPS5674137A (en) * 1979-11-21 1981-06-19 Kyowa Chem Ind Co Ltd Flame-retardant resin composition with improved mechanical strength and agent therefor
JPS56127643A (en) * 1980-03-10 1981-10-06 Showa Electric Wire & Cable Co Ltd Flame-retardant polyolefin composition
JPS596250A (en) * 1982-07-02 1984-01-13 Mitsubishi Rayon Co Ltd Resin composition having excellent surface smoothness

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0414110A2 (en) * 1989-08-21 1991-02-27 The B.F. Goodrich Company Compression molded flame retardant and high impact strength ultra high molecular weight polyethylene composition
JPH05320409A (en) * 1992-05-25 1993-12-03 Matsushita Electric Works Ltd Resinous molding material
JP2010085818A (en) * 2008-10-01 2010-04-15 Inoac Corp Sound absorbing material
CN106739225A (en) * 2016-12-06 2017-05-31 太仓大唐化纤厂 A kind of flame-retardant and anti-static sound insulation composite fiber plate and preparation method thereof

Also Published As

Publication number Publication date
JPH0250141B2 (en) 1990-11-01

Similar Documents

Publication Publication Date Title
KR100564953B1 (en) Flame-retardant resin composition and its use
US5834535A (en) Moldable intumescent polyethylene and chlorinated polyethylene compositions
US6043306A (en) Flame-retardant thermoplastic resin composition
CN111995858B (en) Heat-conducting flame-retardant high-fiber-reinforced polycarbonate composition and preparation method thereof
KR0179442B1 (en) Low-temperature-resistant halogen-free, flame-retardant polyolefin-based resin composition
JPS61174263A (en) Flame-retardant thermoplastic synthtic resin composition for molding film
JP2007056150A (en) Flame retardant resin composition and molded article composed of the same
KR20170006694A (en) Resin composition for automotive wire material and electric wire using it
JP4488578B2 (en) Flame retardant vinyl chloride resin molding
JPH07187744A (en) Sound insulating material of olefinic resin
JP3550184B2 (en) Flame retardant polyolefin resin foam
KR100603055B1 (en) Polypropylene resin composition of complete combustion type
JPH06184372A (en) Flame-retardant polypropylene resin composition
JPH1060192A (en) Flame retardant resin composition and sheet made therefrom
JP3072746B2 (en) Flame retardant resin composition
JPS5920347A (en) Flame-retardant resin composition
JPS5839858B2 (en) Rigid polyvinyl chloride resin composition
KR100624253B1 (en) Composition for production high flame retardant insulating material of halogen free type
JPS6134038A (en) Flame-retarding electrical insulating composition
JPH0493363A (en) Synthetic resin composition
JPH08217953A (en) Phenol resin composition
JP3801657B2 (en) Flame retardant polypropylene resin composition
JPH03265639A (en) Polypropylene resin composition
JPH06128424A (en) Flame-resistant polyolefin resin composition
JPS63308048A (en) Flame-retardant polyolefin composition