JPH0250141B2 - - Google Patents

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Publication number
JPH0250141B2
JPH0250141B2 JP60013860A JP1386085A JPH0250141B2 JP H0250141 B2 JPH0250141 B2 JP H0250141B2 JP 60013860 A JP60013860 A JP 60013860A JP 1386085 A JP1386085 A JP 1386085A JP H0250141 B2 JPH0250141 B2 JP H0250141B2
Authority
JP
Japan
Prior art keywords
film
weight
inorganic
heat
fiber
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 - Lifetime
Application number
JP60013860A
Other languages
Japanese (ja)
Other versions
JPS61174263A (en
Inventor
Takashi Mineo
Makoto Ozawa
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

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Description

【発明の詳細な説明】[Detailed description of the invention]

〓産業上の利用分野〓 本発明は高い強度とタフネスを具え、圧延成型
性にすぐれた難燃性、断熱性、吸音性に富む厚さ
が0.1mmといつた薄膜状難燃性熱可塑性合成樹脂
フイルムに関する。 〓従来の技術〓 従来合成樹脂フイルム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、フイルムの
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。 近年、このような危険性のない無機質の充填材
を、合成樹脂中に充填材してフイルムの難燃化を
計る試みがなされているが、無機質充填材のみを
使用して難燃化を図る場合、樹脂中に多量に配合
することが必要となり、フイルムの強度を劣化し
てフイルムの成型性を低下し厚さが0.1mmといつ
た薄膜状フイルムを得ることはできない。 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。
そのため、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ず、フイ
ルムの成型性は勿論、性能の向上に直接結びつか
ない。 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フイルム
の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、フイルムの難燃性、タフネス
を含め本質的な改善となつていない。 〓発明が解決しようとする課題〓 この発明は従来の合成樹脂の難燃化によつて解
決することのできなかつた、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
よつて起こされる成型性の低下、フイルムの強
度、タフネスの劣化などのない高度の難燃性とタ
フネス及び断熱性、吸音性を具えた薄膜状合成樹
脂フイルムを得ることを目的としている。 〓課題を解決するための手段〓 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5.3〜43重量部を含む無機質充填材40〜70重
量%とを配合混和し、厚さ0.1mmの薄膜状に成型
した。 即ち本発明のフイルムは、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5.3〜43重量部
を含む無機質充填材40〜70重量%とを配合混和
し、押出機を用いて予備成型した後、圧延成型す
ることにより目的とする厚さ0.1mmの薄膜状フイ
ルムを得たものであるが、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、ポリメタク
リル酸エステル、ポリカーボネート、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
40μ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。 更にコロイド状無機繊維としては、チタン酸カ
リ繊維、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、商品名ヘツドマン
繊維(カナダヘツドマン社製)として知られるマ
グネシヤンシリケート系天然無機質繊維等で、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。 然して本発明のフイルムは、前記加熱脱水型無
機質粉末100重量部に対し、コロイド状無機繊維
5.3〜43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℃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、ニーダー、押出機を用い加熱混練法
により混和し、押出機を用いて一旦予備成型した
後、例えばカレンダーロール等の圧延成型機を用
いて厚さ0.1mmの薄膜状に連続圧延成型する。 なお、前記組成物中には、フイルムに要求され
る特性を阻害しない範囲で、公知の熱安定剤、紫
外線安定剤、可塑剤、滑剤、帯電防止剤、増粘
剤、分散剤等を適宜添加配合しても良い。 〓実施例〓 次に本発明のフイルムについて実施例を示すと
共に、得られたフイルムの難燃性を知るための燃
焼性、引張り強さ、伸び、成型性、平滑性を測定
した結果を第1表に示す。
〓Field of Industrial Application〓 The present invention is a thin film-like flame-retardant thermoplastic composite with a thickness of 0.1 mm, which has high strength and toughness, has excellent roll-formability, and is rich in flame retardant, heat-insulating, and sound-absorbing properties. Regarding resin film. 〓Conventional technology〓 Conventional flame retardant technology for synthetic resin films is as follows:
A method of blending flame retardants such as halogen compounds, phosphorus-containing compounds, nitrogen-containing compounds, and antimony oxide with synthetic resin raw materials is used, but such flame retardants are relatively expensive. Moreover, there is a danger that harmful gases may be emitted when the film is formed or exposed to high temperatures. In recent years, attempts have been made to make films flame retardant by using such non-hazardous inorganic fillers as fillers in synthetic resins; In this case, it is necessary to incorporate a large amount into the resin, which deteriorates the strength of the film and reduces the moldability of the film, making it impossible to obtain a thin film with a thickness of 0.1 mm. 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 The amount of inorganic filler used in the synthesis also cannot be reduced to a significant extent.
For this reason, attempts have been made to reduce the amount of inorganic filler blended, but these efforts have not been sufficiently effective and have not directly led to improvements in film moldability or performance. On the other hand, in order to improve the moldability of the film, relatively low molecular weight synthetic resins are sometimes added.
Since low molecular weight synthetic resins have a low softening point, the toughness of the film decreases. In addition, various lubricants and plasticizers such as aluminum stearate and metal soap are sometimes added, but these do not substantially improve the flame retardance and toughness of the film. 〓Problems to be solved by the invention〓 This invention solves problems that could not be solved by conventional flame-retardant synthetic resins, such as the generation of harmful gases that occur during molding or when exposed to high temperatures. The purpose of the present invention is to obtain a thin synthetic resin film that has high flame retardancy, toughness, heat insulation, and sound absorption properties without deterioration of moldability or deterioration of film strength and toughness caused by chemical reaction. 〓Means for solving the problem〓 30-60% by weight of a thermoplastic synthetic resin that does not contain halogen and has a glass transition temperature of 50-120°C, and 5.3 parts by weight of colloidal inorganic fiber for 100 parts by weight of heat-dehydrated inorganic powder. 40 to 70% by weight of an inorganic filler containing ~43 parts by weight was mixed and formed into a thin film with a thickness of 0.1 mm. That is, the film of the present invention has a glass transition temperature of 50
~120°C, 30-60% by weight of halogen-free thermoplastic synthetic resin and 40-70% by weight of inorganic filler containing 5.3-43 parts by weight of colloidal inorganic fiber based on 100 parts by weight of heat-dehydrated inorganic powder. The desired thin film with a thickness of 0.1 mm was obtained by blending and mixing, preforming using an extruder, and rolling molding, but the glass transition temperature used here was 50 ~120°C, halogen-free thermoplastic synthetic resins such as polyethylene, polypropylene, polystyrene, polymethacrylate, polycarbonate, polyethylene terephthalate, and copolymers thereof are advantageously used, and thermally dehydrated inorganic powder The particle size is
Aluminum hydroxide, magnesium hydroxide, hydrated calcium sulfate, or a mixture thereof with a particle size of 40 μ or less is used, and it may be partially replaced with talc, clay, calcium carbonate, etc., as long as it does not impede flame retardancy and moldability. do not have. Furthermore, colloidal inorganic fibers include potassium titanate fiber, boron nitride fiber, calcium metasilicate (wollastonite, sepiolite, magnesian silicate natural inorganic fiber known as Hetdman Fiber (manufactured by Hetdman Co., Ltd., Canada), etc.). The fiber diameter is 3μ or less, the fiber length is 30μ or less, and the aspect ratio is about 10.However, in the film of the present invention, colloidal inorganic fibers are added to 100 parts by weight of the heat-dehydrated inorganic powder.
40 to 70% by weight of an inorganic filler mixed with 5.3 to 43 parts by weight, and 30 to 60% by weight of a halogen-free thermoplastic synthetic resin with a glass transition temperature of 50 to 120°C,
The mixture is mixed by heating and kneading using a pressure roll, kneader, or extruder, and then preformed using an extruder, and then continuously rolled into a thin film with a thickness of 0.1 mm using a rolling machine such as a calendar roll. do. In addition, known heat stabilizers, ultraviolet stabilizers, plasticizers, lubricants, antistatic agents, thickeners, dispersants, etc. may be appropriately added to the composition to the extent that they do not impede the properties required for the film. May be combined. 〓Example〓 Next, an example will be shown about the film of the present invention, and the results of measuring the flammability, tensile strength, elongation, moldability, and smoothness in order to know the flame retardance of the obtained film will be shown in the first part. Shown in the table.

【表】【table】

【表】 水型無機質粉末:水酸化アルミニウム、コロイ
ド状無機繊維:チタン酸カリ繊維
熱可塑性合成樹脂は、密度0.865、エチレン含
量12%の結晶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0.945の高密
度ポリエチレンを使用した。 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
〔商品名ハイジライト、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5μ、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ダーで加熱混練
して押出機を用いて予備成型品を製造した。 次いで該予備成型品をカレンダーロール式圧延
成型機に置き、160℃で5分間加熱加圧した後、
厚さ0.1mmのフイルムを圧延成型し、適宜サイズ
に裁断したものを難燃性を試験するための難燃性
の測定、および引張り強さを測定するための試料
とし、それぞれ5枚ずつ用意した。 難燃性の測定は運輸省「車輌用材料燃焼試験規
格FMVSS−302」に準拠する水平着火式のフレ
ーム法で行ない、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。 引張強さは前記と同様にして成型された厚さ
0.1mmのフイルムを15mm幅に裁断して引張試験を
行ない、15mm幅での破断強度および破断時伸長度
で表示した。 成型性の確認は押出機による予備成型装置付の
カレンダーロール式圧延成型機を用い0.1mm厚の
フイルムを連続成型する時の成型適性と成型後の
フイルムの平滑性で判定し、下記の記号区分によ
り表示した。 成型性 ◎ 容易に成型できるもの 〇 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 〇 フイツシユアイが少量あるが使用上問題がな
いもの △ ピンホール、フイツシユアイがあり、地相不
良のみられるもの × 穴、こぶ等があり使用に耐えないもの 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、フイルム成型性、
フイルム平滑性共に急速に悪化し圧延成型時フイ
ルムが破断したり裂開する。 これに対し、熱可塑性合成樹脂30〜60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%配合し、押
出機を用いて一旦予備成型した後、圧延成型した
本発明のフイルムは、無機質充填材の量が増加す
る程難燃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、フイルムの
成型性、フイルム平滑性に問題はなく、安定した
生産が可能となり、然も無機充填材の量が多い
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。 そして無機質充填材の量が40重量%未満となる
と難燃性に問題を生じ、70重量%を超えるとフイ
ルムの破断強度が低下し、フイルムの平滑性も悪
化してフイルムの破断、裂開を起こす。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5.3重量%未満のときは加熱脱水型無
機粉末に対するコロイド状無機繊維の割合が減少
するため、フイルム中に占める微粉子粉末の量が
増加し、コロイド状無機繊維によるフイルムの強
化が認められず、フイルムの強度が低下すると共
にフイルムの成型性及び表面平滑性が悪化し、43
重量%を超えると、加熱脱水型無機粉末に対する
コロイド状無機繊維の割合が増加するため、コロ
イド状無機繊維同志の重なり合い、絡み合い部分
が増加してフイルムの成型性、及び表面平滑性を
悪化し、厚味の均一な、薄い、実用に耐える強度
等の特性を持つたフイルムを得ることができな
い。 〓発明の効果〓 以上詳細に述べた通り、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5.3〜43重量部を含
む無機質充填材40〜70重量%とを配合混和し、厚
さ0.1mmの薄膜状に成型した本発明のフイルムは、
フイルム成型性特に圧延成型により0.1mmといつ
た薄膜状に成型することができ、得られたフイル
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、高い強度やタフネスを具え、難燃性、
断熱性、吸音性に富み、特に内装材の表面化粧用
フイルムとして使用すると顕著な効果を発揮する
ものである。
[Table] Water type inorganic powder: Aluminum hydroxide, Colloidal inorganic fiber: Potassium titanate fiber The thermoplastic synthetic resin used was a crystalline polypropylene ethylene copolymer with a density of 0.865 and an ethylene content of 12%. used high-density polyethylene with a density of 0.945. As the heat-dehydrated inorganic powder that is one component of the inorganic filler, aluminum hydroxide (trade name: Hygilite, manufactured by Showa Denko K.K.) with an average particle size of 30 μm was used. However, in Examples 2-4 and 5-5, calcium carbonate having an average particle size of 30 μm was used. The colloidal inorganic fiber, which is the other component of the inorganic filler, is a colloidal potassium titanate fiber with a fiber diameter of 3μ or less, fiber length of 30μ or less, and an aspect ratio of 10 [trade name:
manufactured by Otsuka Chemical Co., Ltd.], and in Example 5-5, glass fiber powder with an average fiber diameter of 5 μm and an average fiber length of 100 μm was used. Each composition was heated and kneaded using a pressure kneader, and a preformed product was produced using an extruder. Next, the preformed product was placed in a calendar roll type rolling molding machine, heated and pressed at 160°C for 5 minutes, and then
Films with a thickness of 0.1 mm were rolled and molded, and cut into appropriate sizes, which were used as samples for flame retardancy testing and tensile strength measurements, and five sheets of each were prepared. . Flame retardancy was measured using the horizontal ignition flame method in accordance with the Ministry of Transport's ``Vehicle Material Combustion Test Standard FMVSS-302.'' Each sample was measured five times, the times for the five measurements were added, and the total number of seconds was displayed. The tensile strength is the thickness molded in the same manner as above.
A 0.1 mm film was cut to a width of 15 mm, a tensile test was conducted, and the strength at break at a width of 15 mm and elongation at break were expressed. Confirmation of moldability is determined by the moldability when continuously molding a 0.1 mm thick film using a calendar roll type rolling molding machine equipped with a preforming device using an extruder and the smoothness of the film after molding, and is classified into the following symbol categories. Displayed by. Moldability ◎ Easily moldable 〇 Suitable for molding △ Can be made into sheets continuously regardless of appearance × Things that cannot be molded Smoothness ◎ Extremely smooth 〇 There is a small amount of hard eyes, but this is a problem in use Items that do not have △ Items that have pinholes, hard eyes, and poor topography × Items that have holes, bumps, etc. and are unusable As is clear from this table, heat-dehydrated inorganic materials are used as inorganic fillers for thermoplastic synthetic resins. When mixing only powder, the higher the mixing ratio, the lower the flammability and the higher the flame retardancy, but the lower the breaking strength and elongation, and the lower the film formability.
The smoothness of the film rapidly deteriorates and the film breaks or tears during rolling. On the other hand, 40-70% by weight of an inorganic filler consisting of heat-dehydrated inorganic powder and colloidal inorganic fiber is mixed with 30-60% by weight of thermoplastic synthetic resin, and after being preformed using an extruder, The film of the present invention that has been rolled and molded shows that as the amount of inorganic filler increases, the flame retardance decreases and the flame retardance improves, the breaking strength increases slightly, and the degree of elongation at break decreases, but There is no problem in film properties and film smoothness, and stable production is possible.Moreover, the greater the amount of inorganic filler, the lower the flammability, that is, the higher the flame retardance, and the higher the breaking strength. If the amount of inorganic filler is less than 40% by weight, flame retardant problems will occur, and if it exceeds 70% by weight, the breaking strength of the film will decrease, and the smoothness of the film will also deteriorate, causing the film to break or tear. wake up In addition, when the amount of colloidal inorganic fiber is less than 5.3% by weight based on 100 parts by weight of heat-dehydrated inorganic powder, the proportion of colloidal inorganic fiber to heat-dehydrated inorganic powder decreases, so the fine powder that occupies the film decreases. The amount of colloidal inorganic fibers increases, the film is not strengthened by the colloidal inorganic fibers, the strength of the film decreases, and the formability and surface smoothness of the film deteriorate.
If it exceeds % by weight, the ratio of colloidal inorganic fibers to the heat-dehydrated inorganic powder increases, resulting in an increase in the number of overlapping and entangling portions of colloidal inorganic fibers, which deteriorates the formability and surface smoothness of the film. It is not possible to obtain a film with characteristics such as uniform thickness, thinness, and strength sufficient for practical use. 〓Effects of the invention〓 As described in detail above, the glass transition temperature is 50~
Halogen-free thermoplastic resin at 120℃
30 to 60 parts by weight of inorganic filler containing 5.3 to 43 parts by weight of colloidal inorganic fibers to 100 parts by weight of heat-dehydrated inorganic powder are blended and mixed to form a thin film with a thickness of 0.1 mm. The film of the present invention molded into
Film formability Particularly, it can be formed into a thin film with a thickness of 0.1 mm by rolling.The obtained film has excellent surface smoothness, is flame retardant, does not emit harmful gases, and is made of inorganic materials. The combination of fillers, especially heat-dehydrated inorganic powder and colloidal inorganic fibers, provides high strength and toughness, as well as flame retardancy and
It has excellent heat-insulating and sound-absorbing properties, and is especially effective when used as a surface decorative film for interior materials.

Claims (1)

【特許請求の範囲】[Claims] 1 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5.3〜43重量部を含む無機質充填材40〜70
重量%とを配合混和し、厚さ0.1mmの薄膜状に成
型した難燃性熱可塑性合成樹脂フイルム。
1. Inorganic filler containing 30-60% by weight of a thermoplastic synthetic resin with a glass transition temperature of 50-120°C and no halogen, and 5.3-43 parts by weight of colloidal inorganic fiber per 100 parts by weight of heat-dehydrated inorganic powder. Material 40~70
A flame-retardant thermoplastic synthetic resin film formed into a thin film with a thickness of 0.1 mm.
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 JPS61174263A (en) 1986-08-05
JPH0250141B2 true 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)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Family Cites Families (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

Also Published As

Publication number Publication date
JPS61174263A (en) 1986-08-05

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