JPH05295190A - Polypropylene resin composition - Google Patents

Polypropylene resin composition

Info

Publication number
JPH05295190A
JPH05295190A JP10119392A JP10119392A JPH05295190A JP H05295190 A JPH05295190 A JP H05295190A JP 10119392 A JP10119392 A JP 10119392A JP 10119392 A JP10119392 A JP 10119392A JP H05295190 A JPH05295190 A JP H05295190A
Authority
JP
Japan
Prior art keywords
polypropylene resin
weight
resin composition
flow rate
molded product
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
JP10119392A
Other languages
Japanese (ja)
Inventor
Takashi Uda
隆 宇田
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui 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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP10119392A priority Critical patent/JPH05295190A/en
Publication of JPH05295190A publication Critical patent/JPH05295190A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide the objective compsn. having a high heat distortion temp. and improved bending modulus, impact strength, and gloss by compounding a specific PP resin with a BaSO4 powder and a nucleating agent. CONSTITUTION:100 pts.wt. PP resin comprising 60-95wt.% propylene homopolymer having a melt flow rate (JIS K 7210, 230 deg.C, 2.16kgf-load) of 1-30g/10min, a number-average mol.wt. of 10,000-50,000, and a density of 0.88-0.92g/cm<3> and 5-40wt.% ethylene-propylene block copolymer having a melt flow rate of 1-30g/10min and a number-average mol.wt. of 10,000-100,000 is compounded with 10-50 pts.wt. BaSO4 powder having a mean particle size of 0.04-0.7mum and 0.1-3 pts.wt. nucleating agent.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、ポリプロピレン系樹脂
組成物に関する。
TECHNICAL FIELD The present invention relates to a polypropylene resin composition.

【0002】[0002]

【従来の技術】ポリプロピレン系樹脂は、曲げ弾性率、
耐衝撃性等の機械的強度や耐熱性が優れているので、様
々な成形品に使用されている。しかし成形品が大型にな
るとさらに高い曲げ弾性率や耐衝撃性が要求され、屋外
で使用される成形品においては、高い熱変形温度が要求
されている。これらの問題を解決するために特開平1−
129052号公報には、ポリプロピレン系樹脂にタル
ク、マイカ、ガラス繊維等を添加することが記載されて
いる。
2. Description of the Related Art Polypropylene resin has a flexural modulus,
Since it has excellent mechanical strength such as impact resistance and heat resistance, it is used in various molded products. However, as the size of a molded product becomes larger, higher flexural modulus and impact resistance are required, and a molded product used outdoors requires a high heat distortion temperature. In order to solve these problems, JP-A-1-
Japanese Patent No. 129052 describes adding talc, mica, glass fiber and the like to a polypropylene resin.

【0003】[0003]

【発明が解決しようとする課題】しかし、タルク、マイ
カ等が添加されたポリプロピレン系樹脂組成物から得ら
れた成形体は、ポリプロピレン系樹脂単独から得られた
成形体に比べれば曲げ弾性率は向上しているが、耐衝撃
性及び光沢度が低下している。又、ガラス繊維が添加さ
れたポリプロピレン系樹脂組成物から得られた成形体
は、熱変形温度は向上しているが、表面の光沢度が低下
しており、雨樋、自動車部材等の大型で表面の光沢を要
求される成形品には使用できなかった。
However, a molded product obtained from a polypropylene resin composition to which talc, mica, etc. are added has a higher flexural modulus than a molded product obtained from a polypropylene resin alone. However, the impact resistance and glossiness are deteriorated. Further, the molded product obtained from the polypropylene resin composition to which the glass fiber is added has an improved heat distortion temperature, but the glossiness of the surface is lowered, and it is large in rain gutters, automobile parts, etc. It could not be used for molded products requiring surface gloss.

【0004】本発明の目的は、上記課題を解決し、曲げ
弾性率、耐衝撃性などの機械的強度が優れ、熱変形温度
が高くかつ表面性に優れた成形体を得ることが出来る、
ポリプロピレン系樹脂組成物を提供することにある。
The object of the present invention is to solve the above-mentioned problems and to obtain a molded article which is excellent in mechanical strength such as flexural modulus and impact resistance, has a high heat deformation temperature and is excellent in surface property.
A polypropylene resin composition is provided.

【0005】[0005]

【課題を解決するための手段】本発明において用いられ
るポリプロピレン系樹脂は、プロピレン単独重合体とエ
チレンプロピレン系ブロック共重合体からなる。上記プ
ロピレン単独重合体はメルトフローレートが小さくなる
と成形が難しくなり、大きくなると硫酸バリウム粉末の
分散が不良となるだけでなく、たとえば射出成形により
成形体を得るときには成形時にばりが発生し、押出成形
により成形体を得るときには押出された混練物の引取が
困難になるなどの問題が発生するので、JIS K 7
210に準拠して測定された230℃、2.16kgf
の荷重下におけるメルトフローレートが1〜30g/1
0分が好ましい。曲げ弾性率の高い成形体を得るために
はプロピレン単独重合体の数平均分子量は10,000
〜50,000が好ましい。プロピレン単独重合体は密
度が0.88〜0.92g/cm3 の結晶性のものが好まし
い。非晶質プロピレン単独重合体が添加されると得られ
る成形体の衝撃強度は高くなるが、成形体の弾性率が低
下するので、非晶質プロピレン単独重合体の添加量はポ
リプロピレン系樹脂中30重量%以下が好ましい。非晶
質プロピレン単独重合体の数平均分子量は1,000〜
50,000が好ましい。非晶質プロピレン単独重合体
の密度は0.85〜0.87g/cm3 が好ましい。
The polypropylene resin used in the present invention comprises a propylene homopolymer and an ethylene propylene block copolymer. When the melt flow rate of the propylene homopolymer becomes small, molding becomes difficult, and when it becomes large, not only the dispersion of the barium sulfate powder becomes poor, but also when obtaining a molded product by injection molding, burrs occur at the time of molding and extrusion molding. Therefore, when a molded product is obtained, problems such as difficulty in taking out the extruded kneaded product occur. Therefore, JIS K 7
230 ° C measured according to 210, 2.16 kgf
Melt flow rate under 1 to 30g / 1
0 minutes is preferred. The number average molecular weight of the propylene homopolymer is 10,000 in order to obtain a molded product having a high flexural modulus.
~ 50,000 is preferred. The propylene homopolymer is preferably crystalline and has a density of 0.88 to 0.92 g / cm 3 . When the amorphous propylene homopolymer is added, the impact strength of the obtained molded article increases, but the elastic modulus of the molded article decreases, so the addition amount of the amorphous propylene homopolymer is 30% in the polypropylene resin. It is preferably not more than wt%. The number average molecular weight of the amorphous propylene homopolymer is 1,000 to
50,000 is preferred. The density of the amorphous propylene homopolymer is preferably 0.85 to 0.87 g / cm 3 .

【0006】上記エチレンプロピレン系ブロック共重合
体は、エチレン含有量が少なくなると成形体の衝撃強度
が低くなり、多くなると成形体の弾性率が低くなるの
で、エチレン含有量はエチレンプロピレン系ブロック共
重合体中5〜30重量%が好ましい。エチレンプロピレ
ン系ブロック共重合体のメルトフローレートは低くなる
と成形が難しくなり、高くなると硫酸バリウム粉末の分
散が不良となるだけでなく、たとえば射出成形により成
形体を得るときには成形時にばりが発生し、押出成形に
より成形体を得るときには押出された混練物の引取が困
難になるなどの問題が発生するので、JIS K 72
10に準拠して測定された230℃、2.16kgfの
荷重下におけるメルトフローレートが1〜30g/10
分が好ましい。エチレンプロピレン系ブロック共重合体
の数平均分子量は10,000〜100,000が好ま
しい。
In the above ethylene propylene block copolymer, the impact strength of the molded product decreases as the ethylene content decreases, and the elastic modulus of the molded product decreases as the ethylene content increases. Therefore, the ethylene content depends on the ethylene propylene block copolymer. It is preferably 5 to 30% by weight in the combined product. When the melt flow rate of the ethylene propylene block copolymer becomes low, molding becomes difficult, and when it becomes high, not only the dispersion of the barium sulfate powder becomes poor, but also burrs are generated at the time of molding when obtaining a molded article by injection molding, When a molded product is obtained by extrusion molding, problems such as difficulty in collecting the extruded kneaded product occur. Therefore, JIS K 72
Melt flow rate under a load of 2.16 kgf at 230 ° C. measured in accordance with 10 is 1 to 30 g / 10
Minutes are preferred. The number average molecular weight of the ethylene propylene block copolymer is preferably 10,000 to 100,000.

【0007】エチレンプロピレン系ブロック共重合体の
添加量は、少なくなると成形体の衝撃強度が低くなり、
多くなると成形体の曲げ弾性率が低くなるので、ポリプ
ロピレン系樹脂中5〜40重量%に限定され、好ましく
は10〜30重量%である。
When the amount of the ethylene propylene block copolymer added is small, the impact strength of the molded product becomes low,
Since the flexural modulus of the molded product decreases as the amount increases, it is limited to 5 to 40% by weight, preferably 10 to 30% by weight in the polypropylene resin.

【0008】本発明において用いられる硫酸バリウム粉
末の、平均粒径は小さくなると成形時に粒子が凝集して
分散性が悪くなり、得られる成形体の衝撃強度が低くな
り、大きくなると得られる成形体の曲げ弾性率が低くな
るので、0.04〜0.7μmに限定され、好ましくは
0.1〜0.6μmである。
When the average particle size of the barium sulfate powder used in the present invention is small, the particles aggregate during molding and the dispersibility is poor, and the impact strength of the resulting molded article is low, and when it is large, the resulting molded article is Since the flexural modulus decreases, it is limited to 0.04 to 0.7 μm, preferably 0.1 to 0.6 μm.

【0009】硫酸バリウム粉末の添加量は少なくなると
得られる成形体の曲げ弾性率が低くなり、多くなると成
形体の衝撃強度が低くなるので、ポリプロピレン系樹脂
100重量部に対し、10〜50重量部に限定され、好
ましくは20〜40重量部である。
If the amount of barium sulfate powder added is small, the flexural modulus of the resulting molded article will be low, and if it is too large, the impact strength of the molded article will be low. Therefore, 10 to 50 parts by weight relative to 100 parts by weight of the polypropylene resin. And is preferably 20 to 40 parts by weight.

【0010】本発明において用いられる造核剤は、ポリ
プロピレン系樹脂の結晶の核となって、結晶を成長させ
るのに効果のある物質ならば特に限定されず、たとえば
ジベンジリデンソルビトール、アジピン酸、安息香酸ナ
トリウムなどがあげられる。さらにポリプロピレン樹脂
そのものに高エネルギー電子線を照射して得られた架橋
ポリプロピレン樹脂が使用されてもよい。これらは単独
で使用されてもよいし、2種類以上併用されてもよい。
The nucleating agent used in the present invention is not particularly limited as long as it is a substance which becomes a nucleus of the polypropylene resin crystals and is effective in growing the crystals, and examples thereof include dibenzylidene sorbitol, adipic acid and benzoic acid. Examples include sodium acidate. Further, a crosslinked polypropylene resin obtained by irradiating the polypropylene resin itself with a high energy electron beam may be used. These may be used alone or in combination of two or more kinds.

【0011】造核剤の添加量は少なくなると成形の際に
ポリプロピレン系樹脂の結晶化が進まず、得られる成形
体の曲げ弾性率が低くなり、多くなると得られる成形体
の衝撃強度が低くなるので、ポリプロピレン系樹脂10
0重量部に対し、0.1〜3重量部に限定され、好まし
くは0.2〜1重量部である。
When the amount of the nucleating agent added is small, the crystallization of the polypropylene resin does not proceed during molding and the flexural modulus of the resulting molded article is low, and when it is large, the impact strength of the resulting molded article is low. So, polypropylene-based resin 10
It is limited to 0.1 to 3 parts by weight, preferably 0.2 to 1 part by weight, relative to 0 parts by weight.

【0012】本発明においては、さらに必要に応じて得
られる成形体の衝撃強度、熱変形温度、組成物の熱流動
性等を著しく損なわない範囲で、従来から使用されてい
るポリイソブチレン等の耐衝撃改良材、炭酸カルシウ
ム、炭酸カルシウム、珪酸カルシウム、タルク、マイ
カ、クレー、炭酸マグネシウム、アルミナ、シリカ、硫
酸カルシウム、珪砂、水酸化アルミニウム、水酸化マグ
ネシウム、塩基性炭酸マグネシウム、ゼオライト、黒
鉛、水酸化カルシウム、亜硫酸カルシウム、石英、ベン
トナイト、アスベスト、炭素繊維、金属ウィスカー、ガ
ラス繊維、ガラスビ−ズ、ガラス粉末、ガラスフレーク
等の無機質充填材、スチレン・ブタジエンゴム、1,2-ポ
リブタジエン、ブチルゴム、スチレン・ブタジエン・ス
チレンブロック共重合体、ニトリル・ブタジエンゴム、
ポリイソブチレン、ポリブタジエン、ポリイソプレン、
エチレン以外のα−オレフィンとポリプロピレンとの共
重合体、ポリプロピレン以外のα−オレフィンの単独重
合体、ポリプロピレン以外のα−オレフィン同士の共重
合体、エチレン・酢酸ビニル共重合体、無水マレイン酸
グラフトポリエチレン等のα−オレフィン系グラフト重
合体、ポリアミド、ポリカーボネート、アクリロニトリ
ル・ブタジエン・スチレン樹脂、ポリ塩化ビニル、ポリ
フェニレンエーテル等の熱可塑性樹脂、酸化防止剤、滑
剤、着色剤、紫外線吸収剤、帯電防止剤、分散剤、中和
剤、可塑剤、発泡剤、難燃剤、架橋剤などが添加されて
もよい。
In the present invention, the impact resistance, heat distortion temperature, heat flowability of the composition, etc. of the molded product obtained as required are not impaired, and the resistance of polyisobutylene, etc., which has been conventionally used, is improved. Impact modifier, calcium carbonate, calcium carbonate, calcium silicate, talc, mica, clay, magnesium carbonate, alumina, silica, calcium sulfate, silica sand, aluminum hydroxide, magnesium hydroxide, basic magnesium carbonate, zeolite, graphite, hydroxide Inorganic fillers such as calcium, calcium sulfite, quartz, bentonite, asbestos, carbon fiber, metal whiskers, glass fiber, glass beads, glass powder, glass flakes, styrene-butadiene rubber, 1,2-polybutadiene, butyl rubber, styrene- Butadiene / styrene block copolymer, Nitrile-butadiene rubber,
Polyisobutylene, polybutadiene, polyisoprene,
Copolymer of α-olefin other than ethylene and polypropylene, homopolymer of α-olefin other than polypropylene, copolymer of α-olefins other than polypropylene, ethylene / vinyl acetate copolymer, maleic anhydride grafted polyethylene Α-olefin-based graft polymer such as polyamide, polycarbonate, acrylonitrile butadiene styrene resin, polyvinyl chloride, thermoplastic resin such as polyphenylene ether, antioxidant, lubricant, colorant, ultraviolet absorber, antistatic agent, A dispersant, a neutralizing agent, a plasticizer, a foaming agent, a flame retardant, a crosslinking agent, etc. may be added.

【0013】本発明のポリプロピレン系樹脂組成物の製
造方法は特に限定されるものではなく、従来公知の任意
の方法が採用され、たとえばプロピレン単独重合体、エ
チレンプロピレン系ブロック共重合体、硫酸バリウム粉
末及び造核剤を一軸押出機、二軸押出機、バンバリーミ
キサー、ロール、ブラベンダープラフトグラフ、ニーダ
ー、プラストミルなどの通常の混練機で混練することに
より得ることができる。
The method for producing the polypropylene resin composition of the present invention is not particularly limited, and any conventionally known method may be employed. For example, propylene homopolymer, ethylene propylene block copolymer, barium sulfate powder. And the nucleating agent can be obtained by kneading with a usual kneading machine such as a single-screw extruder, a twin-screw extruder, a Banbury mixer, a roll, a Brabender platograph, a kneader or a plastomill.

【0014】本発明のポリプロピレン系樹脂組成物から
成形体を得る方法は特に限定されるものではなく、従来
公知の任意の方法が採用され、たとえば押出成形法、射
出成形法、吹込み成形法、圧縮成形法、真空成形法など
が使用される。
The method for obtaining a molded product from the polypropylene resin composition of the present invention is not particularly limited, and any conventionally known method can be adopted, for example, extrusion molding method, injection molding method, blow molding method, A compression molding method, a vacuum molding method or the like is used.

【0015】[0015]

【実施例】本発明の詳細を実施例をもって説明する。 実施例1〜3、比較例1〜5 表1に示した所定量の結晶性ポリプロピレン単独重合体
(三菱油化社製、商品名;MA2A、メルトフローレー
ト25g/10分、数平均分子量30,000、密度
0.90g/cm3)、非晶質ポリプロピレン単独重合体
(イーストマンケミカル社製、商品名;M−5H、メル
トフローレート15g/10分、数平均分子量4,40
0、密度0.85g/cm3)、エチレンプロピレンビロ
ック共重合体(三菱油化社製、商品名;BC8、エチレ
ン含有量9重量%、数平均分子量57,000、メルト
フローレート1.8g/10分)、ポリエチレン(旭化
成社製、商品名;サンテックM1820)、硫酸バリウ
ム粉末1(平均粒径0.6μm)、硫酸バリウム粉末2
(平均粒径0.8μm)、硫酸バリウム粉末3(平均粒
径0.06μm)、タルク(ソブエクレー社製、商品
名;ミストロンベーパー:平均粒径3μm)及びジベン
ジリデンソルビトールをプラストミル(東洋精密社製)
で5分間混練し、ポリプロピレン系樹脂組成物を得た。
得られた組成物を加熱プレス機で温度210℃、圧力1
50kg/cm3 で成形し、150mm×150mm×
3.2mmの成形体を得た。
EXAMPLES Details of the present invention will be described with reference to examples. Examples 1 to 3 and Comparative Examples 1 to 5 Predetermined amount of crystalline polypropylene homopolymer (trade name; MA2A, manufactured by Mitsubishi Yuka Co., Ltd., melt flow rate 25 g / 10 minutes, number average molecular weight 30, 000, density 0.90 g / cm 3 ), amorphous polypropylene homopolymer (manufactured by Eastman Chemical Co., trade name; M-5H, melt flow rate 15 g / 10 minutes, number average molecular weight 4,40).
0, density 0.85 g / cm 3 ), ethylene propylene vilock copolymer (manufactured by Mitsubishi Petrochemical Co., Ltd., trade name; BC8, ethylene content 9% by weight, number average molecular weight 57,000, melt flow rate 1.8 g / 10 minutes), polyethylene (made by Asahi Kasei, trade name; Suntec M1820), barium sulfate powder 1 (average particle size 0.6 μm), barium sulfate powder 2
(Average particle size 0.8 μm), barium sulfate powder 3 (average particle size 0.06 μm), talc (manufactured by Sobueclay, trade name; Mistron Vapor: average particle size 3 μm) and dibenzylidene sorbitol plastomill (Toyo Seimitsu Co., Ltd.) Made)
And kneaded for 5 minutes to obtain a polypropylene resin composition.
The composition obtained is heated at a temperature of 210 ° C. under a pressure of 1
Molded at 50 kg / cm 3 , 150 mm × 150 mm ×
A 3.2 mm molded body was obtained.

【0016】得られた成形体を用いて、曲げ弾性率、ア
イゾット衝撃強度、熱変形温度及び光沢度を下記方法で
測定し、結果を表2に示した。
The flexural modulus, Izod impact strength, heat distortion temperature and glossiness of the molded product thus obtained were measured by the following methods, and the results are shown in Table 2.

【0017】曲げ弾性率 得られた成形体を切断し、長さ120mm、幅12.7
mm、厚み3.2mmの試験片を得、ASTM D−7
90に準拠して、曲げ弾性率を測定した。
Flexural Modulus The obtained molded body was cut into a length of 120 mm and a width of 12.7.
mm, thickness 3.2 mm test piece was obtained, ASTM D-7
According to 90, the flexural modulus was measured.

【0018】アイゾット衝撃強度 得られた成形体を切断し、中央部に曲率半径0.25m
mのノッチを有する、長さ65mm、幅12.7mm、
厚み3.2mmの試験片を得、ASTM D−256に
準拠して、アイゾット衝撃強度を測定した。
Izod impact strength The obtained molded body was cut, and the central portion had a radius of curvature of 0.25 m.
65 mm long, 12.7 mm wide, with m notches
A test piece having a thickness of 3.2 mm was obtained, and the Izod impact strength was measured according to ASTM D-256.

【0019】熱変形温度 得られた成形体を切断して試験片を得、JIS K 7
207に準拠して荷重4.6kg/cm2 で熱変形温度
を測定した。
Heat Deformation Temperature A test piece was obtained by cutting the obtained molded body, and JIS K 7
According to 207, the heat distortion temperature was measured with a load of 4.6 kg / cm 2 .

【0020】光沢度 得られた成形体を切断して試験片を得、JIS K 7
105に準拠して入射角60°、反射角60°で光沢度
を測定した。
Glossiness The obtained molded product was cut to obtain a test piece, and JIS K 7
According to 105, the glossiness was measured at an incident angle of 60 ° and a reflection angle of 60 °.

【0021】[0021]

【表1】 [Table 1]

【0022】[0022]

【表2】 [Table 2]

【0023】[0023]

【発明の効果】本発明のポリプロピレン系樹脂組成物
は、上述のとおり、ポリプロピレン単独重合体とエチレ
ンプロピレン系ブロック共重合体からなるポリプロピレ
ン系樹脂、特定の平均粒径の硫酸バリウム粉末及び造核
剤からなるものであるから、曲げ弾性率、衝撃強度及び
熱変形温度が優れ、かつ光沢度の高い成形体を得ること
ができる。
As described above, the polypropylene resin composition of the present invention comprises a polypropylene resin composed of a polypropylene homopolymer and an ethylene propylene block copolymer, barium sulfate powder having a specific average particle diameter, and a nucleating agent. Therefore, it is possible to obtain a molded article having excellent flexural modulus, impact strength and heat distortion temperature and high gloss.

【0024】従って、得られた成形体は、雨樋、自動車
部材等の大型成形品にも好適に使用される。
Therefore, the obtained molded product is suitably used for large-sized molded products such as rain gutters and automobile members.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 プロピレン単独重合体60〜95重量%
とエチレンプロピレン系ブロック共重合体5〜40重量
%からなるポリプロピレン系樹脂100重量部、平均粒
径が0.04〜0.7μmの硫酸バリウム粉末10〜5
0重量部及び造核剤0.1〜3重量部からなることを特
徴とするポリプロピレン系樹脂組成物。
1. Propylene homopolymer 60 to 95% by weight
100 parts by weight of a polypropylene resin composed of 5 to 40% by weight of ethylene propylene block copolymer and barium sulfate powder 10 to 5 having an average particle diameter of 0.04 to 0.7 μm.
A polypropylene resin composition comprising 0 parts by weight and 0.1 to 3 parts by weight of a nucleating agent.
JP10119392A 1992-04-21 1992-04-21 Polypropylene resin composition Pending JPH05295190A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10119392A JPH05295190A (en) 1992-04-21 1992-04-21 Polypropylene resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10119392A JPH05295190A (en) 1992-04-21 1992-04-21 Polypropylene resin composition

Publications (1)

Publication Number Publication Date
JPH05295190A true JPH05295190A (en) 1993-11-09

Family

ID=14294118

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10119392A Pending JPH05295190A (en) 1992-04-21 1992-04-21 Polypropylene resin composition

Country Status (1)

Country Link
JP (1) JPH05295190A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7417087B2 (en) 2001-09-14 2008-08-26 Sumitomo Chemical Company, Limited Process for producing resin composition using powder of aluminum-containing inorganic compound having specific BET surface area and pore volume and resin composition obtained according to said process

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7417087B2 (en) 2001-09-14 2008-08-26 Sumitomo Chemical Company, Limited Process for producing resin composition using powder of aluminum-containing inorganic compound having specific BET surface area and pore volume and resin composition obtained according to said process

Similar Documents

Publication Publication Date Title
CA1335127C (en) Thermoplastic resin composition
JP3255243B2 (en) Polystyrene resin composition
CN105315542B (en) Polyolefin resin molded product, method of manufacturing the same, and air duct using the same
US4914155A (en) Thermoplastic resin composition
JP3039560B2 (en) Thermoplastic resin composition and use thereof
JP2004521983A (en) Flame retardant syndiotactic polystyrene resin composition
JPH0762175A (en) Thermoplastic resin composition
JP2009067969A (en) Thermoplastic polymer composition
JP2000017120A (en) Thermoplastic resin composition
JPH05295190A (en) Polypropylene resin composition
JP2574168B2 (en) Propylene polymer composition
JPS63113047A (en) Resin composition
JP2020122102A (en) Resin composition and injection molding
JP3300442B2 (en) Method for improving impact resistance of thermoplastic resin molded article and composition therefor
JPS59184237A (en) Propylene polymer composition
JPH073083A (en) Production of polyphenylene ether resin composition
JPH06136202A (en) Polypropylene resin composition and its production
JP7537873B2 (en) Foam material containing polyphenylene sulfide polymer (PPS)
JP3480022B2 (en) Thermoplastic elastomer composition
WO2020189681A1 (en) Polycarbonate resin composition, production method therefor, masterbatch pellet, and molded body
JPH08259750A (en) Production of fiber-reinforced polypropylene composition
JP2006016418A (en) Polyolefin composition and molded product composed of the same
JPH08113685A (en) Heat-resistant vinyl chloride resin composition
JPH06256555A (en) Polypropylene resin foamed product
JPH06192490A (en) Thermoplastic resin composition and resin molding