JPS646656B2 - - Google Patents
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- Publication number
- JPS646656B2 JPS646656B2 JP58145779A JP14577983A JPS646656B2 JP S646656 B2 JPS646656 B2 JP S646656B2 JP 58145779 A JP58145779 A JP 58145779A JP 14577983 A JP14577983 A JP 14577983A JP S646656 B2 JPS646656 B2 JP S646656B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- less
- ethylene
- mfi
- composition
- 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.)
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- 239000004743 Polypropylene Substances 0.000 claims description 24
- -1 polypropylene Polymers 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 17
- 229920001155 polypropylene Polymers 0.000 claims description 17
- 229920001971 elastomer Polymers 0.000 claims description 13
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 9
- 239000005977 Ethylene Substances 0.000 claims description 9
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 7
- 239000004711 α-olefin Substances 0.000 claims description 6
- 239000000155 melt Substances 0.000 claims description 5
- 241000357292 Monodactylus Species 0.000 claims 1
- 238000000071 blow moulding Methods 0.000 description 9
- 239000000945 filler Substances 0.000 description 9
- 238000000465 moulding Methods 0.000 description 7
- 229920002943 EPDM rubber Polymers 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000010445 mica Substances 0.000 description 4
- 229910052618 mica group Inorganic materials 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003484 crystal nucleating agent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920006027 ternary co-polymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は、ポリプロピレン組成物に関し、詳細
には結晶性ポリプロピレン、エチレン―α―オレ
フイン共重合体ゴムおよび充填剤とからなる剛
性、耐衝撃性に優れ、特に耐ドローダウン性の良
好な大型ブロー成形に適したポリプロピレン組成
物に関する。
従来、ポリプロピレンは、軽比重、高剛性で耐
熱性、耐薬品性等に優れるために各種用途の成形
品に用いられ、その成形法も射出、押出、ブロ
ー、プレスなどの各種の方法が適用されている。
しかし、これら成形法のうちのブロー成形法で
は、比較的物性の似ている高密度ポリエチレンに
比べて、耐ドローダウン性が悪く成形品に偏肉が
発生し易く応用分野の制限、特に大型ブロー成形
に適さないという欠点があつた。また、ポリプロ
ピレンは、ポリエチレンに比べて低温時の衝撃強
度が弱いために応用分野に制限があつた。
本発明は、上記の欠点を改善し、ブロー成形に
おける耐ドローダウン性が良好で、剛性を失うこ
となく耐衝撃性に優れるポリプロピレン組成物を
得ることを目的としてなされたものであつて、本
発明のポリプロピレン組成物は、(イ)メルトフロー
インデツクス(JISK 6758による温度230℃、荷
重2.16Kgの条件で測定、以下MFIという)が0.5
g/10分未満の結晶性ポリプロピレン50〜95重量
%、(ロ)MFIが1.0g/10分以下、エチレン含量20
〜90重量%、ムーニー粘度60〜100のエチレン―
α―オレフイン共重合体ゴム5〜30重量%、およ
び(ハ)充填剤0〜30重量%となり、かつ組成物のメ
ルトフローインデツクスが0.5g/10分以下であ
ることを特徴とするものであり、専らブロー成形
に用いられる。
以下、本発明の構成について詳細に説明する。
本発明において用いる結晶性ポリプロピレンと
しては、アイソタクチツクの結晶性ポリプロピレ
ンであつて、プロピレンの単独重合体またはエチ
レン含有量10モル%以下のプロピレン―エチレン
のランダムもしくはブロツク共重合体であつても
よいが、MFIが0.5g/10分未満、好ましくは0.4
g/10分以下のものである。MFIが0.5g/10分
以上であると、ブロー成形におけるドローダウン
性が激しく、パリソンの長い大型ブロー成形物の
成形が難かしくなる。
本発明において用いるエチレン―α―オレフイ
ン共重合体ゴムとしては、エチレンとα―オレフ
イン、例えばプロピレン、ブテン―1、ヘキセン
―1、オクテン―1などとの共重合体ゴム、また
はエチレン―プロピレンの系に第三成分として非
共役ジエン類、例えばエチリデンノルボルネン、
ジシクロペンタジエン、1,4―ヘキサジエンな
どを共重合させた三元共重合体ゴム(以下
EPDM)などがあげられる。これらのうちでは
エチレン―プロピレン共重合体ゴム(以下EPR)
またはEPDMが好ましい。これらエチレン―α
―オレフイン共重合体ゴムは、MFIが1.0g/10
分以下、好ましくは0.7g/10分以下のものであ
つて、エチレン含有量が20〜90重量%、ムーニー
粘度(JISK―6300ML1+4100℃、以下同)が60〜
100であるものが好ましい。
上記共重合体ゴムのMFIが1.0g/10分を越え
ると耐ドローダウン性が悪くなる。また、エチレ
ン含有量が90重量%を越えるとゴム的性質が不十
分となり得られる成形物の衝撃強度が低下する。
さらに、ムーニー粘度が上記の範囲外で低い場合
は耐ドローダウン性が悪くなり、一方高い場合に
は得られる成形物の剛性が低下するためにともに
好ましくない。
本発明において用いられる充填剤としては、例
えばマイカ、タルク、繊維状ケイ酸カルシウム、
炭酸カルシウム、硫酸バリウム、カオリン、アル
ミナ、炭酸マグネシウム、酸化チタン、シリカ、
カーボンブラツク、ガラス繊維、炭素繊維などが
あげられる。これら充填剤の粒径は0.05〜200μ
で、好ましくは0.1〜100μである。また、充填剤
はポリオレフインとの親和性を改良するために各
種有機シラン化合物で表面処理を行うことができ
る。充填剤は、要求される成形物の形状や機械的
性質により、その種類、粒径、添加量が適宜選択
される。
本発明のポリプロピレン組成物は、前記の結晶
性ポリプロピレン50〜95重量%、エチレン―α―
オレフイン共重合体ゴム5〜30重量%および充填
剤0〜30重量%からなる組成物である。上記組成
物に占めるエチレン―α―オレフイン共重合体ゴ
ムの割合が、5重量%未満では耐ドローダウン性
および得られる成形物の耐衝撃性が改善されず、
一方30重量%を越えると耐ドローダウン性が悪く
なり得られる成形物の剛性、耐熱性などが低下す
る。さらに、充填剤の割合が30重量%を越えると
耐熱性、表面硬度および剛性は向上するものの、
ブロー成形におけるパリソン切断部の融着の悪化
および耐衝撃性が低下するために好ましくない。
次に、本発明の組成物の製造方法は、上記の各
成分を配合し高速ミキサー、バンバリーミキサ
ー、連続ニーダ、単軸または二軸スクリユー押出
機などの混練機を用いて加熱溶融状態で混練する
ことによつて得られる。得られる組成物は、耐ド
ローダウン性のうえからMFIが0.5g/10分以下
であることが好ましい。
なお、各成分の配合、混練に際し、酸化防止
剤、紫外線吸収剤、金属劣化防止剤などの安定
剤、滑剤、帯電防止剤、電気特性改良剤、難燃化
剤、加工性改良剤、顔料、結晶核剤などの各種添
加剤を配合することができる。
以上、本発明のポリプロピレン組成物は、ブロ
ー成形法、プレス成形法、押出成形法、射出成形
法のごとき各種の成形法によつて、容器、中空
物、ボード、シート、球状物、棒状物、パイプな
どの各種の成形物に成形できる。また、本発明の
組成物は、耐ドローダウン性が良好で得られる成
形物は耐衝撃性に優れ、充填剤を配合したものは
特に剛性、耐熱性、表面硬度などが優れるために
大型のブロー成形物、例えばバンパー、パレツ
ト、太陽熱温水器集熱体などの成形用組成物とし
て好適である。
以下に本発明を実施例でさらに具体的に説明す
る。なお、実施例における%は重量を示し、試験
法は次のとおりである。
(1) ドローダウンの評価
大型中空成形機〔石川島播磨重工業社製、
IPB―200C(商品名)〕を使用し、長さ1.6m、
巾0.16m、重さ3Kgのブローバンパーを成形
し、下部肉厚に対する上部肉厚の比が0.8〜1.0
を◎、0.6〜0.8未満を〇、0.6未満、成形不良ま
たは成形不能を×とした。
(2) 曲げ弾性率 ASTM D790
(3) アイゾツト衝撃強度 ASTM D256
3.2mm厚試験片、ノツチ付
実施例 1〜7
MFIが0.35g/10分の結晶性ポリプロピレン
(以下PPという)、EPDM(MFI 0.7g/10分、エ
チレン含有量72%、ムーニー粘度90)、EPR
(MFI 0.7g/10分、エチレン含有量73%、ムー
ニー粘度70)、マイカ(平均粒径100μ)、タルク
(平均粒径5μ)およびアルミナ(平均粒径0.1μ)
を表―1に示す組合せで配合して高速ミキサーで
混合し、得られた混合物を温度200℃に設定した
連続ニーダで溶融混練した後ペレツト化した。得
られたペレツトを用いてブロー成形を行いドロー
ダウンの評価並びに射出成形機を用いて試験片を
成形し、曲げ弾性率およびアイゾツト衝撃強度を
測定し、その結果を表―1に示した。
実施例 8,9
実施例1、2において、MFIが0.35g/10分の
PPに代りMFIが0.25g/10分のPPを用いた以外
は同様にして評価を行い、その結果を表―1に併
記した。
The present invention relates to a polypropylene composition, in particular, a large-sized blow molding composition comprising crystalline polypropylene, ethylene-α-olefin copolymer rubber, and a filler, which has excellent rigidity and impact resistance, and in particular has good drawdown resistance. The invention relates to polypropylene compositions suitable for. Conventionally, polypropylene has been used for molded products for various purposes due to its low specific gravity, high rigidity, and excellent heat resistance and chemical resistance, and various molding methods such as injection, extrusion, blowing, and pressing have been applied. ing.
However, among these molding methods, blow molding has poor drawdown resistance compared to high-density polyethylene, which has relatively similar physical properties, and tends to cause uneven thickness in molded products, which limits its application, especially in large-scale blow molding. The drawback was that it was not suitable for molding. In addition, polypropylene has a lower impact strength at low temperatures than polyethylene, which limits its field of application. The present invention has been made for the purpose of improving the above-mentioned drawbacks and obtaining a polypropylene composition that has good drawdown resistance in blow molding and has excellent impact resistance without losing rigidity. The polypropylene composition has (a) a melt flow index (measured according to JISK 6758 at a temperature of 230°C and a load of 2.16 kg, hereinafter referred to as MFI) of 0.5.
50-95% by weight of crystalline polypropylene less than g/10 min, (b) MFI less than 1.0 g/10 min, ethylene content 20
~90% by weight, ethylene with Mooney viscosity 60-100
5 to 30% by weight of α-olefin copolymer rubber and (c) 0 to 30% by weight of filler, and the melt flow index of the composition is 0.5 g/10 minutes or less. Yes, used exclusively for blow molding. Hereinafter, the configuration of the present invention will be explained in detail. The crystalline polypropylene used in the present invention is isotactic crystalline polypropylene, and may be a propylene homopolymer or a propylene-ethylene random or block copolymer with an ethylene content of 10 mol% or less, MFI less than 0.5g/10min, preferably 0.4
g/10 minutes or less. If the MFI is 0.5 g/10 minutes or more, the drawdown during blow molding will be severe, making it difficult to mold a large blow molded product with a long parison. The ethylene-α-olefin copolymer rubber used in the present invention is a copolymer rubber of ethylene and α-olefin, such as propylene, butene-1, hexene-1, octene-1, etc., or an ethylene-propylene based copolymer rubber. and non-conjugated dienes, such as ethylidene norbornene, as a third component.
Ternary copolymer rubber (hereinafter referred to as
EPDM), etc. Among these, ethylene-propylene copolymer rubber (hereinafter referred to as EPR)
Or EPDM is preferred. These ethylene-α
-MFI of olefin copolymer rubber is 1.0g/10
minutes or less, preferably 0.7 g/10 minutes or less, with an ethylene content of 20 to 90% by weight and a Mooney viscosity (JISK-6300ML 1+4 100℃, hereinafter the same) of 60 to 90%.
100 is preferred. If the MFI of the copolymer rubber exceeds 1.0 g/10 minutes, the drawdown resistance will deteriorate. Furthermore, if the ethylene content exceeds 90% by weight, the rubber properties will be insufficient and the impact strength of the resulting molded product will be reduced.
Furthermore, if the Mooney viscosity is low outside the above range, the drawdown resistance will be poor, while if it is high, the rigidity of the molded product obtained will be reduced, both of which are undesirable. Examples of fillers used in the present invention include mica, talc, fibrous calcium silicate,
Calcium carbonate, barium sulfate, kaolin, alumina, magnesium carbonate, titanium oxide, silica,
Examples include carbon black, glass fiber, and carbon fiber. The particle size of these fillers is 0.05~200μ
The thickness is preferably 0.1 to 100μ. Further, the filler can be surface-treated with various organic silane compounds in order to improve its affinity with polyolefin. The type, particle size, and amount of the filler to be added are appropriately selected depending on the required shape and mechanical properties of the molded article. The polypropylene composition of the present invention comprises 50 to 95% by weight of the above-mentioned crystalline polypropylene, ethylene-α-
The composition consists of 5-30% by weight of olefin copolymer rubber and 0-30% by weight of filler. If the proportion of the ethylene-α-olefin copolymer rubber in the composition is less than 5% by weight, the drawdown resistance and the impact resistance of the resulting molded product will not be improved;
On the other hand, if it exceeds 30% by weight, the drawdown resistance will deteriorate and the resulting molded product will have lower rigidity, heat resistance, etc. Furthermore, when the proportion of filler exceeds 30% by weight, heat resistance, surface hardness and rigidity improve;
This is undesirable because it worsens the fusion of the cut portion of the parison during blow molding and reduces impact resistance. Next, the method for producing the composition of the present invention involves blending the above-mentioned components and kneading them in a heated molten state using a kneading machine such as a high-speed mixer, Banbury mixer, continuous kneader, single-screw or twin-screw extruder, etc. obtained by The resulting composition preferably has an MFI of 0.5 g/10 minutes or less from the viewpoint of drawdown resistance. In addition, when blending and kneading each component, stabilizers such as antioxidants, ultraviolet absorbers, and metal deterioration inhibitors, lubricants, antistatic agents, electrical property improvers, flame retardants, processability improvers, pigments, Various additives such as crystal nucleating agents can be blended. As described above, the polypropylene composition of the present invention can be produced into containers, hollow objects, boards, sheets, spherical objects, rod-shaped objects, etc. by various molding methods such as blow molding, press molding, extrusion molding, and injection molding. Can be molded into various molded objects such as pipes. In addition, the composition of the present invention has good drawdown resistance, and the resulting molded products have excellent impact resistance, and those containing fillers have particularly excellent rigidity, heat resistance, and surface hardness, so they can be used for large blowdowns. It is suitable as a composition for molding molded articles such as bumpers, pallets, solar water heater heat collectors, etc. The present invention will be explained in more detail below using Examples. In addition, % in an example shows weight, and the test method is as follows. (1) Evaluation of drawdown Large-scale blow molding machine [manufactured by Ishikawajima Harima Heavy Industries Co., Ltd.
IPB-200C (product name)], length 1.6m,
A blow bumper with a width of 0.16 m and a weight of 3 kg is molded, and the ratio of the upper wall thickness to the lower wall thickness is 0.8 to 1.0.
◎, 0.6 to less than 0.8 as ○, less than 0.6, poor molding or unmoldability as ×. (2) Flexural modulus ASTM D790 (3) Izot impact strength ASTM D256 3.2 mm thick test piece, notched Examples 1 to 7 Crystalline polypropylene (hereinafter referred to as PP) with MFI of 0.35 g/10 min, EPDM (MFI 0.7 g/10 min, ethylene content 72%, Mooney viscosity 90), EPR
(MFI 0.7g/10min, ethylene content 73%, Mooney viscosity 70), mica (average particle size 100μ), talc (average particle size 5μ) and alumina (average particle size 0.1μ)
were blended in the combinations shown in Table 1 and mixed in a high-speed mixer, and the resulting mixture was melt-kneaded in a continuous kneader set at a temperature of 200°C and then pelletized. The obtained pellets were blow molded to evaluate drawdown, and test pieces were molded using an injection molding machine to measure the flexural modulus and Izot impact strength. The results are shown in Table 1. Examples 8 and 9 In Examples 1 and 2, the MFI was 0.35 g/10 min.
Evaluations were conducted in the same manner except that PP with an MFI of 0.25 g/10 minutes was used instead of PP, and the results are also listed in Table 1.
【表】
比較例 1〜7
比較のために、実施例で用いたものと同じPP、
EPDM、タルク、マイカおよびアルミナを用い
て、PP単独の場合(比較例1)および表―2に
示す割合で配合した場合(比較例2〜5)並びに
PPのMFIが0.6g/10分および1.0g/10分のもの
を配合した場合(比較例6、7)についても同様
の評価を行い、その結果を表―2に示した。[Table] Comparative Examples 1 to 7 For comparison, the same PP as used in the example,
Using EPDM, talc, mica, and alumina, when PP is used alone (Comparative Example 1), when it is mixed in the proportions shown in Table 2 (Comparative Examples 2 to 5), and
Similar evaluations were conducted for the cases in which PP with MFI of 0.6 g/10 min and 1.0 g/10 min (Comparative Examples 6 and 7) were blended, and the results are shown in Table 2.
【表】【table】
【表】
比較例 8,9
比較のために、実施例1で用いたものと同じ
PP(MFI 0.35g/10分、PP―1)、EPDM、タ
ルク、マイカを用い、さらにMEI 23g/10分の
結晶性ポリプロピレン(PP―2)を配合したも
のについても同様の評価を行い、その結果を表―
3に示した。[Table] Comparative Examples 8 and 9 For comparison, the same as used in Example 1
A similar evaluation was conducted for a product containing PP (MFI 0.35 g/10 min, PP-1), EPDM, talc, mica, and a mixture of crystalline polypropylene (PP-2) with an MEI of 23 g/10 min. Display the results.
Shown in 3.
【表】【table】
Claims (1)
未満の結晶性ポリプロピレン50〜95重量%、およ
び(ロ)メルトフローインデツクスが1.0g/10分以
下、エチレン含量20〜90重量%、ムーニー粘度60
〜100のエチレン―α―オレフイン共重合体ゴム
5〜30重量%とからなり、かつ組成物のメルトフ
ローインデツクスが0.5g/10分以下であること
を特徴とするブロー成形用ポリプロピレン組成
物。1 (a) 50 to 95% by weight of crystalline polypropylene with a melt flow index of less than 0.5 g/10 min, and (b) a melt flow index of 1.0 g/10 min or less, ethylene content of 20 to 90 wt%, Moony viscosity 60
-100 ethylene-α-olefin copolymer rubber in an amount of 5 to 30% by weight, and the composition has a melt flow index of 0.5 g/10 minutes or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58145779A JPS6038449A (en) | 1983-08-11 | 1983-08-11 | Polypropylene composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58145779A JPS6038449A (en) | 1983-08-11 | 1983-08-11 | Polypropylene composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6038449A JPS6038449A (en) | 1985-02-28 |
JPS646656B2 true JPS646656B2 (en) | 1989-02-06 |
Family
ID=15392969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58145779A Granted JPS6038449A (en) | 1983-08-11 | 1983-08-11 | Polypropylene composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6038449A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3301455A2 (en) | 2016-09-29 | 2018-04-04 | Toyota Jidosha Kabushiki Kaisha | Angular velocity measuring device and relative angular velocity measuring device |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH064733B2 (en) * | 1986-02-03 | 1994-01-19 | 日本石油化学株式会社 | Highly rigid and impact resistant polyolefin resin composition |
JPH0680139B2 (en) * | 1986-04-04 | 1994-10-12 | 三井東圧化学株式会社 | Inorganic filler-containing polypropylene resin composition |
US4732926A (en) * | 1986-09-29 | 1988-03-22 | General Motors Corporation | Dry blendable polypropylene composition |
JP3300442B2 (en) * | 1992-12-28 | 2002-07-08 | 三井化学株式会社 | Method for improving impact resistance of thermoplastic resin molded article and composition therefor |
KR100241276B1 (en) * | 1997-08-27 | 2000-02-01 | 정몽규 | A polypropylene resin composition and manufacturing method thereof |
KR20010010674A (en) * | 1999-07-22 | 2001-02-15 | 이내현 | Polypropylene composition for photo album embo sheet |
JP5201784B2 (en) * | 2005-07-01 | 2013-06-05 | 旭有機材工業株式会社 | Propylene-based resin composition for piping members, and piping members and multilayer piping members molded using the same |
CN101213250B (en) * | 2005-07-01 | 2012-06-13 | 旭有机材工业株式会社 | Propylene resin composition for piping member, piping member molded by using same, and multilayer piping member |
EP4444792A1 (en) * | 2021-12-08 | 2024-10-16 | Dow Global Technologies LLC | Thermoplastic polyolefin and molded article therefrom |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4942456A (en) * | 1972-08-26 | 1974-04-22 | ||
JPS574888Y2 (en) * | 1979-05-04 | 1982-01-29 |
-
1983
- 1983-08-11 JP JP58145779A patent/JPS6038449A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3301455A2 (en) | 2016-09-29 | 2018-04-04 | Toyota Jidosha Kabushiki Kaisha | Angular velocity measuring device and relative angular velocity measuring device |
Also Published As
Publication number | Publication date |
---|---|
JPS6038449A (en) | 1985-02-28 |
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