JPH02199146A - Polypropylene resin composition for injection molding - Google Patents

Polypropylene resin composition for injection molding

Info

Publication number
JPH02199146A
JPH02199146A JP1883589A JP1883589A JPH02199146A JP H02199146 A JPH02199146 A JP H02199146A JP 1883589 A JP1883589 A JP 1883589A JP 1883589 A JP1883589 A JP 1883589A JP H02199146 A JPH02199146 A JP H02199146A
Authority
JP
Japan
Prior art keywords
injection molding
parts
pts
resin composition
impact resistance
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
JP1883589A
Other languages
Japanese (ja)
Inventor
Tsugunori Sugiura
杉浦 嗣典
Masaomi Goto
正臣 後藤
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.)
Toyoda Gosei Co Ltd
Original Assignee
Toyoda Gosei 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 Toyoda Gosei Co Ltd filed Critical Toyoda Gosei Co Ltd
Priority to JP1883589A priority Critical patent/JPH02199146A/en
Publication of JPH02199146A publication Critical patent/JPH02199146A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the title composition to which a melt index(MI) suitable for injection molding can be imparted without lowering its normal-temperature impact resistance by adding an amorphous polyolefin to a base composition formed by adding talc to a polymer blend of a crystalline polypropylene with an ethylene/propylene rubber. CONSTITUTION:100 pts.wt. polymer component (a blend formed by blending polypropylene with an ethylene/propylene rubber in a weight ratio of 9/1-5/5) is mixed with 2-15 pts.wt. inorganic filler (entirely or mainly consists of talc of a mean particle diameter of 0.4-4mum) and 2-15 pts.wt., desirably 5-10 pts.wt. amorphous poly(alpha-olefin) (of a melt viscosity of 1000-10000cp, desirably 1000-3000cp) to obtain a polypropylene resin composition for injection molding desirable for large and long products requiring high impact resistance, especially automobile bumpers, moldings and the like.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、射出成形用ポリプロピレン樹脂組成物に関す
る。特に、自動車のパンバ、モール等大型ないし長尺で
大きな酎、衝撃性が要求される製品の射出成形用材料と
して好適なものである。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a polypropylene resin composition for injection molding. In particular, it is suitable as an injection molding material for large or long products such as automobile pambas and malls, and products that require impact resistance.

なお、以下の説明で、rP PJはポリプロピレンの、
rEPRJはエチレンプロピレンゴム系ポリマーの、r
MIJはメルト・インデックスのそれぞれの略号である
In addition, in the following explanation, rP PJ is polypropylene,
rEPRJ is an ethylene propylene rubber-based polymer, r
MIJ is the respective abbreviation for Melt Index.

また、配合単位は、特にことわらない限り、重量単位で
ある。Mlの値は、JIS K 7210 (A法、条
件:試験温度230℃、試験荷重2.16kgf )に
基づくもので、単位g/10分は省略して表示する、耐
衝撃強度の値は、JISに7110に規定するアイゾツ
トgI!試験方法に基づくものである。
Moreover, the compounding unit is a weight unit unless otherwise specified. The value of Ml is based on JIS K 7210 (Method A, conditions: test temperature 230°C, test load 2.16kgf), and the unit g/10 minutes is omitted.The value of impact resistance is based on JIS Izot gI specified in 7110! It is based on the test method.

〈従来の技術〉 上記バンバのような自動車用成形品は、軽量化および耐
衝撃性向上の目的から、結晶性PPにEPRを混合した
ポリマーブレンドを主成分とするポリマー成分を使用し
、さらに、剛性向上の目的から、タルク等の無機充填剤
が適宜量配合された基本組成を有する射出成形用pp樹
脂組成物を用いて、射出成形により製造していた。
<Prior art> Automotive molded products such as the above-mentioned Bamba use a polymer component whose main component is a polymer blend of crystalline PP mixed with EPR for the purpose of reducing weight and improving impact resistance. For the purpose of improving rigidity, it was manufactured by injection molding using a pp resin composition for injection molding having a basic composition containing an appropriate amount of an inorganic filler such as talc.

〈発明が解決しようとする課題〉 しかし、上記射出成形に際して、製品に所要の強度、特
に常温における耐衝撃性(例えば、常温耐衝撃強度50
 kgf−cm/ rats以上)を得ようとすると、
結晶性PPとしてメルト・インデックス(Mりの小さい
もの(例えば、Ml値20未満のもの)、即ち、高分子
量のものを使用する必要がある。このため、上記EPR
や無機充填剤を配合したPP樹脂組成物(成形材料)の
MIも射出成形に適した値(通常10〜20)より小さ
くなり成形性に問題を生じた。
<Problems to be Solved by the Invention> However, during the above injection molding, the required strength of the product, especially impact resistance at room temperature (for example, impact resistance at room temperature of 50
kgf-cm/rats or more),
As crystalline PP, it is necessary to use one with a low melt index (Ml value (for example, one with an Ml value of less than 20), that is, one with a high molecular weight.
The MI of the PP resin composition (molding material) containing an inorganic filler and an inorganic filler was also smaller than a value suitable for injection molding (usually 10 to 20), causing problems in moldability.

即ち、通常の射出圧力(300kg/cm”)では、材
料流れが悪いため、ショートショット(充填不良)が発
生し、また、ショートショットを回避するため、射出圧
力を過大とすると、大量のパリが発生しやすい、この傾
向は、射出ゲート部から材料流れ最終部位までの距離が
長い大型成形品の場合、特に顕著となる。
In other words, with normal injection pressure (300 kg/cm"), short shots (filling defects) occur due to poor material flow, and if the injection pressure is set too high to avoid short shots, a large amount of paris will be generated. This tendency, which is likely to occur, is particularly noticeable in the case of large-sized molded products in which the distance from the injection gate to the final part of the material flow is long.

本発明は、上記にかんがみて、諸物性の大きな低下、特
に常温耐衝撃性の大きな低下を招くことなく、射出成形
に適したMlを有する射出成形用PP樹脂組成物を提供
することを目的とする。
In view of the above, an object of the present invention is to provide a PP resin composition for injection molding which has an Ml suitable for injection molding without causing a large decrease in various physical properties, especially a large decrease in room temperature impact resistance. do.

く課題を解決するための手段〉 本発明者らは、上記にm題を解決するために、鋭意開発
に努力をした結果、下記構成の射出成形用PP樹脂組成
物に想到した。
Means for Solving the Problems> In order to solve the above problems, the present inventors have made extensive efforts in development and have come up with a PP resin composition for injection molding having the following structure.

結晶性PPとEPRとが前者/後者=971〜515の
配合比からなるポリマーブレンドを全成分または主成分
とするポリマー成分100部に対して、平均粒径0.5
〜4μmのタルクを全成分または主成分とする無機充填
剤が5〜20部配合された基本組成を有し、非晶性ポリ
αオレフィンが前記ポリマー成分100部に対して2〜
15部配合されてなる射出成形用PP樹脂組成物。
An average particle size of 0.5 for 100 parts of a polymer component whose entire or main component is a polymer blend consisting of crystalline PP and EPR in a blending ratio of the former/latter = 971 to 515.
It has a basic composition in which 5 to 20 parts of an inorganic filler whose entire or main component is talc of ~4 μm is blended, and 2 to 20 parts of amorphous poly-α-olefin is added to 100 parts of the polymer component.
A PP resin composition for injection molding containing 15 parts.

〈手段の詳細な説明〉 本発明の射出成形用PP樹脂組成物は、下記(1)のポ
リマー成分と(2)の無機充填剤とからなる基本組成の
ものに、下記(3)の非晶性ポリαオレフィンを添加し
たものである。
<Detailed explanation of means> The PP resin composition for injection molding of the present invention has a basic composition consisting of the following polymer component (1) and the inorganic filler (2), and the following amorphous (3). This product contains poly-α-olefin.

(1)ポリマー成分: 結晶性ppとEPRとが前者/後者=9/1〜515(
望ましくは、8/2〜6/4)の配合比からなるポリマ
ーブレンドを全成分または主成分とする。
(1) Polymer component: Crystalline pp and EPR are former/latter = 9/1 to 515 (
Preferably, the total or main component is a polymer blend having a blending ratio of 8/2 to 6/4.

EPRの配合量が上記より過少であると製品の低温の耐
衝撃性を向上させることができず、上記より過剰となる
と、製品に実用強度(例えば、引張強度で140kgf
101’以上)が得がたくそれぞれ望ましくない。
If the amount of EPR is less than the above, it will not be possible to improve the low-temperature impact resistance of the product, and if it is in excess, the product will have a practical strength (for example, tensile strength of 140 kgf).
101' or more) is difficult to obtain and is therefore undesirable.

ここで結晶性PPには、プロピレン単独重合体、プロピ
レン−エチレン共重合体を含むが、望ましくは、エチレ
ン含量5〜lO%のプロピレン−エチレン共重合体が、
低温耐**性および実用強度を得る見地から望ましい、
また、結晶性PPのMlの範囲は10〜30であること
が望ましい、10未満では成形性に、30を超えると常
温耐衝撃性にそれぞれ問題を生じやすい。
Here, the crystalline PP includes a propylene homopolymer and a propylene-ethylene copolymer, but preferably a propylene-ethylene copolymer with an ethylene content of 5 to 10%,
Desirable from the standpoint of obtaining low temperature resistance** and practical strength.
Further, it is desirable that the Ml of the crystalline PP is in the range of 10 to 30. If it is less than 10, problems tend to occur in moldability, and if it exceeds 30, problems tend to occur in room temperature impact resistance.

EPRは、エチレンプロピレンツポリマー、エチレンプ
ロピレンジェンターポリマーいずれでもよい、ここでE
PRのムーニー粘度の範囲は、lO〜30ML、や、 
(100℃)であるが望ましい。
EPR may be either an ethylene propylene polymer or an ethylene propylene terpolymer, where E
The Mooney viscosity range of PR is 1O~30ML, and
(100°C) is desirable.

10未満では、低温耐衝撃性に悪影響がでやすく、30
を超えると結晶性PPとの相溶性が低下して、成形不良
が発生しやすい。
If it is less than 10, low-temperature impact resistance is likely to be adversely affected;
If it exceeds this amount, the compatibility with crystalline PP decreases, and molding defects are likely to occur.

なお、このポリマー成分には、高密度ポリエチレンを、
衝撃強度改善等の見地から、適宜量、(通常、ポリマー
成分中に1〜10wt%)配合することができる。
In addition, this polymer component includes high-density polyethylene,
From the viewpoint of improving impact strength, etc., it can be blended in an appropriate amount (usually 1 to 10 wt% in the polymer component).

(2)無機充填剤: 平均粒径0.5〜4μm(望ましくは、1〜3μm)の
タルクを全成分または主成分とするものとする。タルク
以外の無機充填剤を主成分とすると、剛性が低下する。
(2) Inorganic filler: All or the main component is talc with an average particle size of 0.5 to 4 μm (preferably 1 to 3 μm). If the main component is an inorganic filler other than talc, the rigidity will decrease.

副成分として添加可能な無機充填剤としては、炭酸カル
シウム、マイカ等を挙げるこができる。また、粒径が0
.5μm未満では、凝集現象に伴なう分散不良が発生し
やすく、4μmを超えると、表面平滑性が悪くなり、成
形不良となる。
Examples of inorganic fillers that can be added as subcomponents include calcium carbonate and mica. Also, the particle size is 0
.. If it is less than 5 μm, poor dispersion is likely to occur due to agglomeration phenomenon, and if it exceeds 4 μm, surface smoothness deteriorates, resulting in poor molding.

また、タルクの配合量はポリマー成分100部に対して
5〜20部とする。5部未満では、成形品に実用強度を
得がたく、20部を超えると耐衝撃性に悪影響がでる。
The amount of talc to be blended is 5 to 20 parts per 100 parts of the polymer component. If it is less than 5 parts, it will be difficult to obtain practical strength in the molded product, and if it exceeds 20 parts, impact resistance will be adversely affected.

(3)非晶性ポリαオレフィン: ここで非晶性ポリαオレフィンとは、非晶性PP、非晶
性プロピレン−エチレン共重合体、非晶性プロピレン−
1ブテン共重合体等を挙げることができる。この非晶性
ポリαオレフィンの溶融粘度の範囲は、1000〜10
000 c P (望ましくは、1000〜3000c
 P )であることが望ましい、 1000c p未満
では、耐衝撃性に悪影響がでやすく、実用強度が得がた
くなり、10000 c Pを超えるとMl調製効果が
得がたい。
(3) Amorphous poly-α-olefin: Here, amorphous poly-α-olefin refers to amorphous PP, amorphous propylene-ethylene copolymer, amorphous propylene-ethylene copolymer,
1-butene copolymer and the like can be mentioned. The range of melt viscosity of this amorphous polyα-olefin is 1000 to 10
000cP (preferably 1000~3000c
P ) is desirable.If it is less than 1000 cP, impact resistance is likely to be adversely affected and it becomes difficult to obtain practical strength, and if it exceeds 10000 cP, it is difficult to obtain the Ml adjustment effect.

また、この非晶性ポリαオレフィンは、Ml調製剤とし
ての働きをするもので、その配合量は、目的のM I 
(flに応じてポリマー成分100部に対して2〜15
部(望ましくは、5〜10部)とする、2部未満では、
Mlの調製効果が得られず、15部を超えると耐衝撃性
に悪影響が出やすいとともに実用強度を得がたくなる。
In addition, this amorphous poly-α-olefin functions as an Ml adjuster, and its blending amount is determined to meet the target Ml
(2 to 15 parts per 100 parts of polymer component depending on fl)
parts (preferably 5 to 10 parts), less than 2 parts,
The effect of preparing Ml cannot be obtained, and if it exceeds 15 parts, impact resistance tends to be adversely affected and it becomes difficult to obtain practical strength.

上記構成要件を具備するPP樹脂組成物は、必要により
、安定剤(熱安定剤、紫外線吸収剤、光安定剤等)、離
型剤等の副資材を適宜配合して、混合機・混練機・造粒
機でそれぞれ混合・混練・造粒して射出成形用材料とす
る(第1図参照)。
The PP resin composition having the above-mentioned constituent requirements is prepared by adding auxiliary materials such as stabilizers (thermal stabilizers, ultraviolet absorbers, light stabilizers, etc.) and mold release agents as necessary, and then using a mixer/kneader.・Mix, knead, and granulate each in a granulator to make an injection molding material (see Figure 1).

そして、当該成形用材料を使用して、前述のバンバ、サ
イドモール等の製品を射出成形する。
Then, using the molding material, products such as the above-mentioned bangers and side moldings are injection molded.

〈発明の作用・効果〉 本発明の射出成形用PP樹脂組成物は、結晶性PPとE
PRとが前者/後者=9/1〜515の配合比からなる
ポリマーブレンドを全成分または主成分とするポリマー
成分100部に対して、平均粒径0.5〜4μmのタル
クを全成分または主成分とする無機充填剤が5〜20部
配合された基本組成を有し、非晶性ポリαオレフィンが
前記ポリマー成分100部に対して2〜15部配合され
てなる構成とすることにより、後述の実施例で示す如く
、成形品の諸物性の大きな低下、特に常温耐衝撃性の大
量な低下を招くことなく、射出成形に通したMlを有す
る。
<Actions and effects of the invention> The PP resin composition for injection molding of the present invention comprises crystalline PP and E
talc with an average particle size of 0.5 to 4 μm is added to 100 parts of a polymer component consisting entirely or mainly of a polymer blend with a blending ratio of former/latter = 9/1 to 515. By having a basic composition in which 5 to 20 parts of an inorganic filler as a component are blended, and 2 to 15 parts of amorphous poly-α-olefin are blended with respect to 100 parts of the polymer component, as described below. As shown in Examples, the molded product has a Ml that can be passed through injection molding without causing a large decrease in various physical properties, particularly in room temperature impact resistance.

従って、従来の如く、Ml値が適当でないことにより、
射出成形に際して、ショートショット(充填不良)が発
生したり、又は、大量のパリが発生するようなことは、
はとんどなくなる。
Therefore, as in the past, due to inappropriate Ml value,
During injection molding, short shots (filling defects) or large amounts of flakes should be avoided.
will almost disappear.

〈実施例〉 以下、本発明の効果を確認するために行なった実施例に
ついて、比較例とともに説明をする。
<Examples> Examples carried out to confirm the effects of the present invention will be described below along with comparative examples.

第1表に示す各実施例・比較例の配合処方の材料を、第
1図に示す汎用の方法で、混合・混練・造粒して成形材
料を調製する。
A molding material is prepared by mixing, kneading, and granulating the materials according to the formulations of each Example and Comparative Example shown in Table 1 using the general-purpose method shown in FIG.

こうして得た成形材料は、Mlを測定するとともに、射
出成形機により、射出圧: 300 kg/cm’、ノ
ズル温度;220℃の条件でバンバ成形用金型(金型温
度 23℃)の製品キャビティに注入をして成形を行な
った。
The Ml of the thus obtained molding material was measured, and the molding material was molded into the product cavity of a Banba mold (mold temperature: 23°C) using an injection molding machine at an injection pressure of 300 kg/cm' and a nozzle temperature of 220°C. was injected and molded.

そして、得られた各成形品について、表示の諸物性を測
定した。引張伸び及び引張強さは、それぞれ JIS 
K 7113 (試験片=1号形、引張速度:50I/
■In )に基づいて行なった。また、成形性は、ショ
ート・ショット又はヒケの有無を目視により判定し、無
し−0、有り・・・×、として表示した。
The various physical properties indicated were then measured for each of the obtained molded articles. Tensile elongation and tensile strength are respectively JIS
K 7113 (test piece = No. 1 type, tensile speed: 50I/
■In). Moreover, the moldability was determined visually as to the presence or absence of short shots or sink marks, and the results were expressed as "absent - 0", "present" as "×".

第1表に測定結果を示すが、成形に適したMl値であっ
ても、各実施例の物性は、大きな低下がなく、特に常温
における耐衝撃性がほとんど低下しない(実施例1・2
と比較例1との対比)、これに対して、Ml値の高い結
晶性PPを使用した比較例2・3はいずれも常温耐衝撃
性において大きく低下し、さらに、Ml値が20程度の
結晶性PP(比較例3)では、組成物のMlの調製、す
なわち、成形性の改良は困難であることが分る。
The measurement results are shown in Table 1. Even when the Ml value is suitable for molding, the physical properties of each example do not deteriorate significantly, especially the impact resistance at room temperature hardly decreases (Examples 1 and 2).
(Comparison with Comparative Example 1), whereas Comparative Examples 2 and 3 using crystalline PP with a high Ml value both showed a significant decrease in room temperature impact resistance. It can be seen that in the case of PP (Comparative Example 3), it is difficult to adjust the Ml of the composition, that is, to improve the moldability.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の組成を有する成形材料の汎用の製造方
法を示す工程図である。 特  許  出  願  人 豊田合成株式会社 UatポリブEIJ815HK 三菱ノーブレン QC−2C uBIJリブ0J830HV ショウレックス 56002H JSREP911P タルクLMR100 ^PAO83^15 宇部興産 三菱油化 宇部興産 昭和電工 日本合成ゴム 富士タルク 宇部興産 ブ0ピレンーエチレン共重合体      89&〃 
            − 〃               a電エチレン1吐レ
ンフボリマー    粘度:  15ML4平均位径 
1.8μ■    − 溶融粘度 15OOcP 自 発   補 正 手続補正書 1、事件の表示 平成O1年特許願第018835号 2、発明の名称 射出成形用ポリプロピレン樹脂組成物 3、補正をする者 事件との関係   特 許 出 願 人住所 名称   豊田合成株式会社 4、代理人 住 所 〒460愛知県名古屋市中区栄二丁目it#k
tg号電話 名古屋 (052) 221−7856 
(代衣>−明細書の詳細な説明の欄 6、補正の内容 (1)明細書第11頁を別紙の通り補正する。
FIG. 1 is a process diagram showing a general-purpose manufacturing method for a molding material having the composition of the present invention. Patent application Toyoda Gosei Co., Ltd. Uat Polyb EIJ815HK Mitsubishi Noblen QC-2C uBIJ Rib 0J830HV Showlex 56002H JSREP911P Talc LMR100 ^PAO83^15 Ube Industries Mitsubishi Oil Chemical Ube Industries Showa Denko Japan Synthetic Rubber Fuji Talc Ube Kosan pyrene-ethylene Polymer 89&〃
-〃 A-electroethylene 1-discharge polymer polymer Viscosity: 15ML4 average diameter
1.8μ■ - Melt viscosity 15OOcP Voluntary Written amendment of amendment procedure 1, Indication of the case 1999 Patent Application No. 018835 2, Name of the invention Polypropylene resin composition for injection molding 3, Person making the amendment Relationship with the case Patent Applicant address: Toyoda Gosei Co., Ltd. 4, agent address: Sakae 2-chome, Naka-ku, Nagoya, Aichi Prefecture 460 it#k
TG phone number Nagoya (052) 221-7856
(Yogi>-Detailed explanation column 6, contents of amendment (1) Page 11 of the specification is amended as shown in the attached sheet.

Claims (1)

【特許請求の範囲】  結晶性ポリプロピレンとエチレンプロピレンゴム系ポ
リマーとが前者/後者(重量比)=9/1〜5/5の配
合比からなるポリマーブレンドを全成分または主成分と
するポリマー成分100重量部に対して、平均粒径0.
5〜4μmのタルクを全成分または主成分とする無機充
填剤が5〜20重量部配合された基本組成を有し、 非晶性ポリαオレフィンが前記ポリマー成分100重量
部に対して2〜15重量部配合されてなる、 ことを特徴とする射出成形用ポリプロピレン樹脂組成物
[Scope of Claims] Polymer component 100 whose entire or main component is a polymer blend consisting of crystalline polypropylene and ethylene propylene rubber-based polymer in a blending ratio of the former/latter (weight ratio) = 9/1 to 5/5. Based on parts by weight, the average particle size is 0.
It has a basic composition in which 5 to 20 parts by weight of an inorganic filler whose entire or main component is talc of 5 to 4 μm is blended, and 2 to 15 parts by weight of amorphous polyα-olefin per 100 parts by weight of the polymer component. A polypropylene resin composition for injection molding, comprising: parts by weight.
JP1883589A 1989-01-28 1989-01-28 Polypropylene resin composition for injection molding Pending JPH02199146A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1883589A JPH02199146A (en) 1989-01-28 1989-01-28 Polypropylene resin composition for injection molding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1883589A JPH02199146A (en) 1989-01-28 1989-01-28 Polypropylene resin composition for injection molding

Publications (1)

Publication Number Publication Date
JPH02199146A true JPH02199146A (en) 1990-08-07

Family

ID=11982622

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1883589A Pending JPH02199146A (en) 1989-01-28 1989-01-28 Polypropylene resin composition for injection molding

Country Status (1)

Country Link
JP (1) JPH02199146A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5532309A (en) * 1991-03-28 1996-07-02 Ube Industries, Ltd. Resin composition for automobile bumper
KR100286857B1 (en) * 1998-10-09 2001-04-16 이영일 Atactic polypropylene-based resin composition for reinforcing impact resistance
JP2011042381A (en) * 2009-08-20 2011-03-03 Fuji Seal International Inc Resin-made container

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5532309A (en) * 1991-03-28 1996-07-02 Ube Industries, Ltd. Resin composition for automobile bumper
KR100286857B1 (en) * 1998-10-09 2001-04-16 이영일 Atactic polypropylene-based resin composition for reinforcing impact resistance
JP2011042381A (en) * 2009-08-20 2011-03-03 Fuji Seal International Inc Resin-made container

Similar Documents

Publication Publication Date Title
KR100418018B1 (en) Thermoplastic elastomer composition and method of making same
CA1196166A (en) Method of producing partially crosslinked rubber- resin composition
US5001182A (en) Resin composition for automobile bumper
JP3031022B2 (en) Method for producing thermoplastic elastomer composition
JP5092216B2 (en) Propylene-based resin composition production method, propylene-based resin composition, and injection-molded body comprising the same
KR20020034426A (en) Composition of polypropylene resin
US7655721B2 (en) Method for producing a propylene-based resin composition, a propylene-based resin composition, and an injection molded article
JP3330046B2 (en) Masterbatch for coloring polypropylene-based composite materials
JPH051185A (en) Thermoplastic resin composition excellent in strength and its production
JP2003286383A (en) Polypropylene resin composition and injection-molded object comprising the same
JPH02199146A (en) Polypropylene resin composition for injection molding
JPWO2017111100A1 (en) Injection molded product of polypropylene resin composition
KR100360073B1 (en) Translucent thermoplastic elastomer
JPH05214184A (en) Polypropylene-based resin composition improved in processability
CN102311586B (en) PP/SBR (polypropylene/styrene butadiene rubber) blended modified composite material and preparation method thereof
JP2009270015A (en) Production method of polyolefin resin composition
JPH03137146A (en) Polypropylene-based resin composition
JP2509750B2 (en) Polypropylene resin composition
JP3189477B2 (en) Polypropylene resin molded product
JP2010215747A (en) Propylene-based resin composition and method for producing the same
JP2594544B2 (en) Polypropylene composition
JP3595857B2 (en) Polypropylene resin composition
KR20060123884A (en) Polypropylene resin composition
JP2019163347A (en) Propylene-based resin composition for injection molding and molded body
JP2002146153A (en) Polypropylene resin composition