JP2003064188A - Resin molded product - Google Patents

Resin molded product

Info

Publication number
JP2003064188A
JP2003064188A JP2001261131A JP2001261131A JP2003064188A JP 2003064188 A JP2003064188 A JP 2003064188A JP 2001261131 A JP2001261131 A JP 2001261131A JP 2001261131 A JP2001261131 A JP 2001261131A JP 2003064188 A JP2003064188 A JP 2003064188A
Authority
JP
Japan
Prior art keywords
molded product
resin molded
resin
present
ethylene
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
JP2001261131A
Other languages
Japanese (ja)
Inventor
Satoru Sogabe
覚 宗我部
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP2001261131A priority Critical patent/JP2003064188A/en
Publication of JP2003064188A publication Critical patent/JP2003064188A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To easily provide an inexpensive resin molded product having higher impact strength than conventional ones. SOLUTION: This resin molded product is made of a thermoplastic resin such as a propylene-based resin and has the following characteristics: the aspect ratio for the particle size of the rubber component present in the region corresponding to a thickness of 20 μm from the external surface is >=1.37, the external surface roughness Ra is <=0.125 μm, and the external surface represents the reverse side when viewed from the direction of applying impact on this resin molded product.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、衝撃強度に優れた
樹脂成形品に関する。
TECHNICAL FIELD The present invention relates to a resin molded article having excellent impact strength.

【0002】[0002]

【従来の技術】従来より、熱可塑性樹脂からなる樹脂成
形品は、自動車の内装、外装部品や自動二輪車部品、家
電等の部品に多く利用されているが、該部品に対する基
本的な要求性能の一つとして衝撃性能が挙げられる。衝
撃強度を高めるには、材料面を補強する(例えばポリプ
ロピレンからなる樹脂成形品であればゴムやタルクなど
の充填材を添加する等)方法や、樹脂成形品の構造を工
夫して衝撃を吸収させ、衝撃強度を向上させる方法等が
知られている。
2. Description of the Related Art Conventionally, a resin molded article made of a thermoplastic resin has been widely used for interior and exterior parts of automobiles, motorcycle parts, home appliances and the like. One of them is impact performance. To increase the impact strength, absorb the impact by devising the method of reinforcing the material surface (for example, adding a filler such as rubber or talc for a resin molded product made of polypropylene) and the structure of the resin molded product. There are known methods for improving impact strength.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、かかる
性能向上の要求は際限が無く、より簡便で且つ低コスト
で更なる衝撃強度の改良ができることが望ましい。本発
明の目的は、簡便で且つ低コストで、より衝撃強度に優
れた樹脂成形品を提供することにある。
However, there is no limit to the demand for such performance improvement, and it is desirable that the impact strength can be further improved at a simpler and lower cost. An object of the present invention is to provide a resin molded product which is simple and low in cost, and has excellent impact strength.

【0004】[0004]

【課題を解決するための手段】本発明は、熱可塑性樹脂
からなり、外表面から20μmまでの厚みに存在するゴ
ム成分の粒径のアスペクト比が1.37以上である樹脂
成形品にかかるものである。以下、本発明につき詳しく
説明する。
The present invention relates to a resin molded product which is made of a thermoplastic resin and has an aspect ratio of the particle diameter of the rubber component existing at a thickness of 20 μm from the outer surface of 1.37 or more. Is. Hereinafter, the present invention will be described in detail.

【0005】[0005]

【発明の実施の形態】本発明で用いる熱可塑性樹脂は、
特に限定されるものではなく、例えばエチレン、プロピ
レン、ブテン−1、ペンテン−1、ヘキセン−1、3−
メチルブテン−1、4−メチルペンテン−1などのα−
オレフィンの単独重合体やこれらと共重合が可能な他の
不飽和単量体との共重合体、あるいは炭素数3以上のα
−オレフィンおよびエチレンの中から選ばれる少なくと
も2種類のモノマーからなる共重合体等が挙げられる。
また、これらを単独または2種以上用いてもよい。上記
の中でも、高密度ポリエチレン、中密度ポリエチレン、
低密度ポリエチレン、直鎖状低密度ポリエチレン、エチ
レン−酢酸ビニル共重合体、エチレン−アクリル酸エチ
ル共重合体などのエチレン系樹脂;アイソタクチックポ
リプロピレン、シンジオタクチックポリプロピレンや、
プロピレン−エチレンブロック共重合体またはランダム
共重合体などのプロピレン系樹脂等のオレフィン系樹脂
が好ましい。特に、この中でもプロピレン系樹脂がより
好ましい。
BEST MODE FOR CARRYING OUT THE INVENTION The thermoplastic resin used in the present invention is
It is not particularly limited, for example, ethylene, propylene, butene-1, pentene-1, hexene-1, 3-
Α-, such as methylbutene-1, 4-methylpentene-1
Olefin homopolymers, copolymers with other unsaturated monomers that can be copolymerized with these, or α with 3 or more carbon atoms
-Copolymers and the like composed of at least two kinds of monomers selected from olefin and ethylene.
Moreover, you may use these individually or in 2 or more types. Among the above, high density polyethylene, medium density polyethylene,
Ethylene resins such as low density polyethylene, linear low density polyethylene, ethylene-vinyl acetate copolymer, ethylene-ethyl acrylate copolymer; isotactic polypropylene, syndiotactic polypropylene,
An olefin resin such as a propylene resin such as a propylene-ethylene block copolymer or a random copolymer is preferable. Among these, propylene-based resin is particularly preferable.

【0006】本発明の樹脂成形品はこのような熱可塑性
樹脂からなり、かつ、ゴム成分が分子相溶しない状態で
含有されている。プロピレン−エチレンブロック共重合
体のように、そのようなゴム成分を元々含有している熱
可塑性樹脂を用いる場合は、本発明の熱可塑性樹脂とし
てそのような熱可塑性樹脂をそのまま用いてもよいし、
そのような熱可塑性樹脂および熱可塑性エラストマーか
らなる熱可塑性樹脂組成物も好適に用いられる。また、
前記ゴム成分を含有しない熱可塑性樹脂を用いる場合
は、前記ゴム成分を含有する熱可塑性樹脂となし得る他
の材料を併用する。前記ゴム成分を含有しない熱可塑性
樹脂を用いる場合、好ましくは該熱可塑性樹脂および熱
可塑性エラストマーからなる熱可塑性樹脂組成物が用い
られる。
The resin molded product of the present invention is made of such a thermoplastic resin and contains the rubber component in a state in which it is not molecularly compatible. When using a thermoplastic resin originally containing such a rubber component like a propylene-ethylene block copolymer, such a thermoplastic resin may be used as it is as the thermoplastic resin of the present invention. ,
A thermoplastic resin composition comprising such a thermoplastic resin and a thermoplastic elastomer is also suitably used. Also,
When the thermoplastic resin containing no rubber component is used, another material that can be used as the thermoplastic resin containing the rubber component is also used. When a thermoplastic resin containing no rubber component is used, a thermoplastic resin composition comprising the thermoplastic resin and a thermoplastic elastomer is preferably used.

【0007】熱可塑性エラストマーとしては、例えばオ
レフィン系エラストマーやスチレン系エラストマーが挙
げられ、1種のみを使用しても2種以上を併用してもよ
い。オレフィン系エラストマーとしては、例えばエチレ
ン−プロピレン共重合体ゴム、エチレン−プロピレン−
非共役ジエン系共重合体ゴム、エチレン−ブテン−1共
重合体ゴム、エチレン−ブテン−1−非共役ジエン系共
重合体ゴム、プロピレン−ブタジエン系共重合体ゴム、
エチレン−オクテン系共重合体ゴムのようなオレフィン
を主成分とする無定型ランダムな共重合弾性体が挙げら
れる。非共役ジエンとしては、例えばジシクロペンタジ
エン、1,4−ヘキサジエン、シクロオクタジエン、メ
チルノルボルネン、エチリデンノルボルネン等が挙げら
れる。スチレン系エラストマーとしては、例えばスチレ
ン−ブタジエンブロック共重合体、スチレン−イソプレ
ンブロック共重合体、水素化スチレン−イソプレンブロ
ック共重合体、スチレングラフトエチレン−プロピレン
共重合体ゴム、スチレン−アクリロニトリルグラフトエ
チレン−プロピレン共重合体ゴム、スチレングラフトエ
チレン−プロピレン−非共役ジエン共重合体ゴム、スチ
レン−エチレン−ブチレン−スチレンブロック共重合体
ゴム等が挙げられる。
Examples of the thermoplastic elastomer include olefin elastomers and styrene elastomers, and one kind may be used alone, or two or more kinds may be used in combination. Examples of the olefin elastomer include ethylene-propylene copolymer rubber and ethylene-propylene-
Non-conjugated diene copolymer rubber, ethylene-butene-1 copolymer rubber, ethylene-butene-1-non-conjugated diene copolymer rubber, propylene-butadiene copolymer rubber,
An amorphous random copolymer elastic body containing an olefin as a main component, such as an ethylene-octene copolymer rubber, may be mentioned. Examples of the non-conjugated diene include dicyclopentadiene, 1,4-hexadiene, cyclooctadiene, methylnorbornene, ethylidenenorbornene and the like. Examples of the styrene elastomer include styrene-butadiene block copolymer, styrene-isoprene block copolymer, hydrogenated styrene-isoprene block copolymer, styrene-grafted ethylene-propylene copolymer rubber, styrene-acrylonitrile-grafted ethylene-propylene. Copolymer rubber, styrene-grafted ethylene-propylene-non-conjugated diene copolymer rubber, styrene-ethylene-butylene-styrene block copolymer rubber and the like can be mentioned.

【0008】本発明の樹脂成形品においては、前記ゴム
成分は分子相溶しておらず、電子顕微鏡で観察すると粒
子を形成している。本発明の樹脂成形品は、外表面から
20μmまでの厚みに存在する前記ゴム成分の粒径のア
スペクト比がある水準より大きく、衝撃強度に優れた樹
脂成形品である。本発明の樹脂成形品においては、該ア
スペクト比は平均値で1.37以上であり、好ましくは
1.5〜9.5であり、さらに好ましくは1.7〜9.
3である。
In the resin molded product of the present invention, the rubber components are not molecularly compatible with each other and form particles when observed with an electron microscope. The resin molded product of the present invention is a resin molded product excellent in impact strength, in which the aspect ratio of the particle diameter of the rubber component present in the thickness of 20 μm from the outer surface is larger than a certain level. In the resin molded product of the present invention, the aspect ratio has an average value of 1.37 or more, preferably 1.5 to 9.5, and more preferably 1.7 to 9.
It is 3.

【0009】また本発明の樹脂成形品の外表面は滑らか
であるとより衝撃強度に優れる。本発明の樹脂成形品
は、その外表面の表面粗さRaが好ましくは0.125
μm以下であり、さらに好ましくは0.108μm以下
である。
If the outer surface of the resin molded product of the present invention is smooth, the impact strength is more excellent. The surface roughness Ra of the outer surface of the resin molded product of the present invention is preferably 0.125.
It is less than or equal to μm, and more preferably less than or equal to 0.108 μm.

【0010】本発明においては、上に述べてきた樹脂成
形品の特定の外表面は、樹脂成形品のすべての外表面が
該当してもよいが、樹脂成形品に対して衝撃が加えられ
る方向から見て裏面側の外表面が、上述の特定の外表面
であることが好ましい。
In the present invention, the specific outer surface of the resin molded article described above may be all the outer surfaces of the resin molded article, but the direction in which impact is applied to the resin molded article. It is preferable that the outer surface on the back surface side as viewed from above is the above-described specific outer surface.

【0011】本発明で用いる熱可塑性樹脂には、本発明
の目的を損なわない範囲で無機フィラーを含ませてもよ
い。無機フィラーとしては、例えばタルク、マイカ、ワ
ラストナイト、炭酸カルシウム、硫酸バリウム、炭酸マ
グネシウム、クレー、アルミナ、シリカ、硫酸カルシウ
ム、炭素繊維、ガラス繊維、金属繊維、酸化チタン、カ
ーボンブラック、水酸化マグネシウム、けいそう土等が
挙げられる。これらは1種のみを使用しても2種以上を
併用してもよい。
The thermoplastic resin used in the present invention may contain an inorganic filler as long as the object of the present invention is not impaired. Examples of the inorganic filler include talc, mica, wollastonite, calcium carbonate, barium sulfate, magnesium carbonate, clay, alumina, silica, calcium sulfate, carbon fiber, glass fiber, metal fiber, titanium oxide, carbon black, magnesium hydroxide. , Diatomaceous earth, etc. These may be used alone or in combination of two or more.

【0012】また、本発明で用いる熱可塑性樹脂には、
本発明の目的を損なわない範囲で、酸化防止剤、紫外線
吸収材、滑剤、顔料、帯電防止剤、銅害防止剤、中和
剤、造核剤等の添加剤を含ませることができる。
Further, the thermoplastic resin used in the present invention includes
Additives such as an antioxidant, an ultraviolet absorber, a lubricant, a pigment, an antistatic agent, a copper damage inhibitor, a neutralizing agent and a nucleating agent can be contained within the range not impairing the object of the present invention.

【0013】本発明でいう樹脂成形品とは、上記熱可塑
性樹脂を通常公知の成形法で成形された成形品をいう。
代表的な公知の成形法としては、例えば射出成形、ガス
アシスト射出成形、サンドイッチ射出成形、射出圧縮成
形、射出プレス成形が挙げられ、さらにその他圧縮成
形、ブロー成形、射出ブロー成形、シート成形、熱成形
(真空成形や圧空成形)やフィルム押出成形等も含まれ
る。
The resin molded product referred to in the present invention refers to a molded product obtained by molding the above thermoplastic resin by a generally known molding method.
Typical known molding methods include, for example, injection molding, gas-assisted injection molding, sandwich injection molding, injection compression molding, injection press molding, and other compression molding, blow molding, injection blow molding, sheet molding, heat molding. Molding (vacuum molding and pressure molding) and film extrusion molding are also included.

【0014】射出成形法により本発明の樹脂成形品を得
るには、剪断が大きくかかる条件で成形するとよい。例
えば、以下に示す成形条件のなかの少なくとも1つの手
段により成形される。・金型温度を低くする。・シリン
ダ−温度を低くする。・射出速度を速くする。・粘度の
高い材料を用いる。板厚を薄くする、など。
In order to obtain the resin molded product of the present invention by the injection molding method, it is advisable to carry out the molding under the condition that a large shear is applied. For example, it is molded by at least one of the following molding conditions.・ Lower the mold temperature.・ Cylinder-Lower the temperature.・ Increase the injection speed.・ Use highly viscous materials. Decrease the plate thickness, etc.

【0015】また本発明の樹脂成形品は、通常の成形法
で得られた成形品の外表面を火炎処理することでも得ら
れる。ここでいう火炎の種類および火炎処理の方法はい
かようなものでも良く、例えば、LPG可燃性ガスが充
填されたガスト−チを用いて、樹脂成形品の外表面を所
定時間火炎処理する方法が挙げられる。火炎処理におい
て、火炎処理時間は樹脂成形品が変形しない範囲で通常
実施され、1〜60秒が好ましく、さらに好ましくは2
〜55秒である。さらに、火炎処理時の樹脂成形品表面
温度は600℃以上であることが望ましく、630〜7
00℃がさらに好ましい。
The resin molded product of the present invention can also be obtained by subjecting the outer surface of the molded product obtained by a usual molding method to flame treatment. The type of flame and the method of flame treatment referred to herein may be any, for example, a method of flame treating the outer surface of the resin molded product for a predetermined time using a gas torch filled with an LPG combustible gas. Can be mentioned. In the flame treatment, the flame treatment time is usually carried out within a range in which the resin molded product is not deformed, preferably 1 to 60 seconds, more preferably 2
~ 55 seconds. Furthermore, it is desirable that the surface temperature of the resin molded product during the flame treatment is 600 ° C. or higher.
00 ° C. is more preferable.

【0016】[0016]

【実施例】以下、本発明を実施例および比較例に基づき
説明するが、本発明はこれら実施例・比較例に限定され
るものではない。
EXAMPLES The present invention will be described below based on Examples and Comparative Examples, but the present invention is not limited to these Examples and Comparative Examples.

【0017】<樹脂成形品最表面の観察法>KEYEN
CE社製表面形状観察顕微鏡で樹脂成形品の表面の平均
粗さ状態(Ra)を観察した。
<Observation method of outermost surface of resin molded product> KEYEN
The average roughness state (Ra) of the surface of the resin molded product was observed with a surface shape observation microscope manufactured by CE.

【0018】(樹脂成形品表面近傍モルフォロジ−観察
法>透過型電子顕微鏡(TEM)にて樹脂成形品表面近
傍(最表層から20μm)に存在するゴム成分の粒径を
観察して、それらのアスペクト比を算出した。
(Morphology observation method near the surface of the resin molded product> The particle size of the rubber component existing near the surface of the resin molded product (20 μm from the outermost layer) is observed by a transmission electron microscope (TEM), and their aspect The ratio was calculated.

【0019】<耐衝撃性評価方法>樹脂成形品の中央部
よりの試験片を切出し、該試験片の衝撃強度をBS13
30に準拠して測定した。具体的には、得られた樹脂成
形品を10mm(MD方向)×5mm(TD方向)に切
り出し試験片とした。次いで 衝撃測定装置(ダインス
タットテスタ−:テスタ−産業製)専用のチャックに、
ハンマ−の打撃点が試験片の厚さの1.75倍の位置
(即ち、厚み3mmの試験片の場合は5.25mmの位
置)を打撃する(BS1330に規定)様に調整して、
装着した。次に使用ハンマ−ごとに規定されている角度
にハンマ−を持ち上げ装置のフックに掛け、本体指針を
持ち上げたハンマ−の角度の位置に合わせ、ハンマ−を
フックより外しハンマ−を上述した試験片の打撃点に当
てて、振り上げられたハンマ−の角度をよみBS133
0の規定による計算式により試験片のエネルギ−を算出
した。
<Impact resistance evaluation method> A test piece from the center of the resin molded product was cut out, and the impact strength of the test piece was determined to be BS13.
It measured based on 30. Specifically, the obtained resin molded product was cut into 10 mm (MD direction) × 5 mm (TD direction) to obtain a test piece. Next, on the chuck for exclusive use of the shock measurement device (Dynestat tester: manufactured by Tester Sangyo),
Adjust so that the hammer hits the position of 1.75 times the thickness of the test piece (that is, the position of 5.25 mm for a test piece with a thickness of 3 mm) (specified in BS1330),
I put it on. Next, hang the hammer on the hook of the lifting device at the angle specified for each hammer used, align the main body pointer with the angle position of the lifted hammer, remove the hammer from the hook, and remove the hammer from the test piece described above. Hit the hitting point of and read the angle of the hammer that was swung up BS133
The energy of the test piece was calculated by a calculation formula based on the rule of 0.

【0020】[比較例1]プロピレン−エチレンブロッ
ク共重合体(住友化学工業(株)製、住友ノーブレンA
W564、MFR:30g/10分、降伏強度:278
kgf/cm2 、エチレン−プロピレンランダム共重合
体部の含量=14重量%、エチレン−プロピレンランダ
ム共重合体部のエチレンから誘導される繰り返し単位の
含量=37重量%)を射出成形機(住友重機械(株)
製、ネオマット515/150)にて、成形温度220
℃で、120×120×3mmtの平板を成形した。該
樹脂成形品最表層面の平均表面粗さ(Ra)は0.12
5μmであり、樹脂成形品の外表面から20μmまでに
存在するゴム粒径のアスペクト比は1.0から1.36
であった。この平板の衝撃強度を表1に示す。
[Comparative Example 1] Propylene-ethylene block copolymer (Sumitomo Chemical Co., Ltd., Sumitomo Noblene A)
W564, MFR: 30 g / 10 minutes, yield strength: 278
kgf / cm 2 , content of ethylene-propylene random copolymer part = 14% by weight, content of repeating unit derived from ethylene of ethylene-propylene random copolymer part = 37% by weight), injection molding machine (Sumitomo Heavy Industries) Machinery Co., Ltd.
Made by Neomat 515/150), molding temperature 220
A flat plate of 120 × 120 × 3 mmt was molded at 0 ° C. The average surface roughness (Ra) of the outermost surface of the resin molded product is 0.12.
5 μm, and the aspect ratio of the rubber particle diameter existing from the outer surface of the resin molded product to 20 μm is 1.0 to 1.36.
Met. Table 1 shows the impact strength of this flat plate.

【0021】[実施例1〜3]比較例1と同様にして得
られた樹脂成形品の外表面をLPG可燃性ガスが充填さ
れたガスト−チ(日本瓦斯株式会社製 プリンスガスト
−チ)の火炎にて成形品表面温度650℃で火炎処理し
た。実施例1〜3それぞれの処理時間、火炎処理した表
面の表面粗さ、外表面から20μmまでの厚みに存在す
るゴム成分の粒径のアスペクト比および衝撃強度を測定
した結果を表1に示す。
[Examples 1 to 3] A gas torch (Prince gas torch manufactured by Nippon Gas Co., Ltd.) filled with an LPG combustible gas on the outer surface of a resin molded article obtained in the same manner as in Comparative Example 1 Flame treatment was performed with a flame at a surface temperature of the molded product of 650 ° C. Table 1 shows the results obtained by measuring the treatment time, the surface roughness of the flame-treated surface, the aspect ratio of the particle diameter of the rubber component present in the thickness of 20 μm from the outer surface, and the impact strength of each of Examples 1 to 3.

【0022】[0022]

【表1】 [Table 1]

【0023】[0023]

【発明の効果】以上詳述したように本発明によれば、簡
便で且つ低コストで、より衝撃強度に優れた樹脂成形品
が提供される。
As described above in detail, according to the present invention, there is provided a resin molded product which is simple, low in cost and excellent in impact strength.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4F071 AA02 AA10 AA14 AA15 AA16 AA17 AA18 AA19 AA20 AA21 AB03 AB06 AB18 AB21 AB24 AB26 AB28 AB30 AF23 AG30 AH07 AH11 BA01 BB03 BB05 BB06 BC07 BC10 BC16 4F073 AA06 AA21 BA04 BA06 BA07 BA08 BA09 BA10 BA11 BB02 BB09 GA03 4J002 AA01W AC00X BB01W BB03W BB05W BB06W BB07W BB11X BB12W BB14W BB14X BB15W BB15X BN03X BP01X BP02X FD010 GN00    ─────────────────────────────────────────────────── ─── Continued front page    F-term (reference) 4F071 AA02 AA10 AA14 AA15 AA16                       AA17 AA18 AA19 AA20 AA21                       AB03 AB06 AB18 AB21 AB24                       AB26 AB28 AB30 AF23 AG30                       AH07 AH11 BA01 BB03 BB05                       BB06 BC07 BC10 BC16                 4F073 AA06 AA21 BA04 BA06 BA07                       BA08 BA09 BA10 BA11 BB02                       BB09 GA03                 4J002 AA01W AC00X BB01W BB03W                       BB05W BB06W BB07W BB11X                       BB12W BB14W BB14X BB15W                       BB15X BN03X BP01X BP02X                       FD010 GN00

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】熱可塑性樹脂からなり、外表面から20μ
mまでの厚みに存在するゴム成分の粒径のアスペクト比
が1.37以上である樹脂成形品。
1. A thermoplastic resin, 20 μm from the outer surface
A resin molded product in which the aspect ratio of the particle diameter of the rubber component present in the thickness up to m is 1.37 or more.
【請求項2】外表面の表面粗さRaが、0.125μm
以下である請求項1記載の樹脂成形品。
2. The surface roughness Ra of the outer surface is 0.125 μm.
The resin molded product according to claim 1, which is as follows.
【請求項3】前記外表面が、樹脂成形品に対して衝撃が
加えられる方向から見て裏面側である請求項1または2
記載の樹脂成形品。
3. The outer surface is the back surface side when viewed from the direction in which an impact is applied to the resin molded product.
The resin molded product described.
【請求項4】熱可塑性樹脂がプロピレン系樹脂である請
求項1〜3のいずれかに記載の樹脂成形品。
4. The resin molded product according to claim 1, wherein the thermoplastic resin is a propylene resin.
JP2001261131A 2001-08-30 2001-08-30 Resin molded product Pending JP2003064188A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001261131A JP2003064188A (en) 2001-08-30 2001-08-30 Resin molded product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001261131A JP2003064188A (en) 2001-08-30 2001-08-30 Resin molded product

Publications (1)

Publication Number Publication Date
JP2003064188A true JP2003064188A (en) 2003-03-05

Family

ID=19088220

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001261131A Pending JP2003064188A (en) 2001-08-30 2001-08-30 Resin molded product

Country Status (1)

Country Link
JP (1) JP2003064188A (en)

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