JPH11207772A - Manufacture of automobile injection molded product - Google Patents
Manufacture of automobile injection molded productInfo
- Publication number
- JPH11207772A JPH11207772A JP2921398A JP2921398A JPH11207772A JP H11207772 A JPH11207772 A JP H11207772A JP 2921398 A JP2921398 A JP 2921398A JP 2921398 A JP2921398 A JP 2921398A JP H11207772 A JPH11207772 A JP H11207772A
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- propylene
- injection molding
- filler
- 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
Links
Landscapes
- Injection Moulding Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明はドアトリム、ピラー
トリム等の自動車用射出成形品に係り、特に成形用樹脂
としてフィラ入りエチレン−プロピレン重合体(PP)
を用いた自動車用射出成形品における樹脂組成の改良に
関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to injection molded articles for automobiles such as door trims and pillar trims, and more particularly, ethylene-propylene polymer containing filler (PP) as a molding resin.
The present invention relates to an improvement in a resin composition of an injection molded article for an automobile using the same.
【0002】[0002]
【従来の技術】従来よりドアトリム、ピラートリム等の
自動車用射出成形品にはポリプロピレンが多く用いられ
ている。ポリプロピレンは、多用されている高密度ポリ
エチレンに比較して、耐熱性、耐ストレスクラッキング
性は優れているが、低温衝撃性は弱い。このため従来は
ポリプロピレンにポリエチレンを重合したエチレン−プ
ロピレン重合体を用いてドアトリムやピラートリムの製
造を行なっている。2. Description of the Related Art Conventionally, polypropylene is often used in injection molded articles for automobiles such as door trims and pillar trims. Polypropylene is superior in heat resistance and stress cracking resistance to high-density polyethylene, which is widely used, but has low low-temperature impact resistance. For this reason, conventionally, door trim and pillar trim are manufactured using an ethylene-propylene polymer obtained by polymerizing polyethylene on polypropylene.
【0003】かかる製造方法を図2及び図3に示す。図
2に示す従来技術は先ずペレット状化したエチレン−プ
ロピレン重合体(以下EPP重合体という)を二軸押出
成形機10の入口側ホッパ11に投入して加熱溶融した
後出口側のホッパ12よりフィラ状タルク(微粉状滑り
石)を投入分散させて、タルク入りEPP重合体ペレッ
トを作成し、これを射出成形機5のホッパ6内に投入し
て加熱溶融して型7内に射出成形して所定の成形品を製
造するものである。FIGS. 2 and 3 show such a manufacturing method. In the prior art shown in FIG. 2, first, an ethylene-propylene polymer (hereinafter, referred to as an EPP polymer) in the form of pellets is charged into an inlet hopper 11 of a twin-screw extruder 10, heated and melted, and then discharged from a hopper 12 at an outlet. Filler-like talc (fine-grained talc) is added and dispersed to produce talc-containing EPP polymer pellets, which are charged into a hopper 6 of an injection molding machine 5, heated and melted, and injection-molded into a mold 7. Thus, a predetermined molded product is manufactured.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、かかる
従来法で製造された樹脂部材においては、機械的物性値
や衝撃値はある一定以上あるものの、フィラ状タルクと
EPP重合体との混合に2軸スクリューの様な大型の押
出機を用いねばならず、且つ混練の為の工数もかかりコ
スト高である。この為、図3に示すように、フィラを含
む流動性の極めて高いEPP重合体(フィラ入りマスタ
バッチ)をペレット状化し、該ペレット状化したマスタ
ーバッチと、内装材としての機械的物性値を出すための
PP樹脂とを射出成形機5のホッパ6に投入し、該射出
成形機5内で両者を混合しながら加熱溶融して型7内に
射出成形して所定の成形品を製造する従来技術を用いて
いる。However, in the resin member manufactured by the conventional method, although the mechanical property value and the impact value are not less than a certain value, the mixing of the filler talc and the EPP polymer is biaxial. A large extruder such as a screw must be used, and the man-hours for kneading are high and the cost is high. Therefore, as shown in FIG. 3, an EPP polymer having a very high fluidity including a filler (a master batch containing a filler) is pelletized, and the mechanical properties of the pelletized master batch and the interior material are determined. Conventionally, a PP resin to be discharged is put into a hopper 6 of an injection molding machine 5, heated and melted while mixing the two in the injection molding machine 5 and injection molded into a mold 7 to produce a predetermined molded product. Using technology.
【0005】しかしながらかかる従来技術によれば、大
型の押出機を用いることなく射出成形機5のみで、樹脂
混合を行なうためにコスト安で樹脂成形品を作ることが
出来るが、射出成形機5のみで混合するために、フィラ
の分散が悪く、機械的物性値が低くなる。本発明はかか
る従来技術の欠点に鑑み、大型の押出機を用いることな
く又製造工程の煩雑化を避けつつ充分な機械的物性値、
特に低温衝撃値を向上させたドアトリム、ピラートリム
等の自動車用射出成形品の製造方法を提供することにあ
る。However, according to the prior art, a resin molded product can be produced at low cost by using only the injection molding machine 5 without using a large-sized extruder. , The dispersion of the filler is poor and the mechanical properties are low. In view of the drawbacks of the prior art, the present invention has sufficient mechanical properties without using a large-sized extruder and while avoiding complicated production steps.
In particular, it is an object of the present invention to provide a method of manufacturing an injection molded product for an automobile such as a door trim and a pillar trim having an improved low-temperature impact value.
【0006】[0006]
【課題を解決するための手段】本発明はかかる課題を解
決するために、メルトフローレートが50〜100g/
10分(230℃、荷重:2.16Kgf)で且つプロ
ピレン含有量が80〜99重量%の第1のエチレン−プ
ロピレン重合体と、メルトフローレートが1〜20g/
10分且つプロピレン含有量が30〜60重量%の第2
のエチレン−プロピレン重合体とを押出機で混練して形
成したペレット状混練樹脂体と、該混練樹脂体と平均粒
径2〜6μmのフィラを100:50〜80重量%の割
合で混練してペレット状化したマスタ−バッチとを用意
し、これらの2種の樹脂体を射出成形機5のホッパ6内
に投入して加熱溶融しながら射出成形を行なうことを特
徴とする自動車用射出成形品の製造方法を提案する。
尚、前記第1の重合体と第2の重合体の配合比は60〜
90:10〜40重量%に設定するのがよい。又フィラ
には一般にタルクを用いるのがよく、その粒径は平均粒
径2〜6μmに設定するのがよい。けだし粒径が2μm
以下ではフィラの分散が十分いかず、又6μm以上では
機械的物性値が低下する。In order to solve the above-mentioned problems, the present invention has a melt flow rate of 50 to 100 g / m.
A first ethylene-propylene polymer having a propylene content of 10 to 20 minutes (230 ° C., load: 2.16 Kgf) and a propylene content of 80 to 99% by weight, and a melt flow rate of 1 to 20 g /
10 minutes and the second having a propylene content of 30 to 60% by weight.
A kneaded resin body formed by kneading an ethylene-propylene polymer with an extruder and a filler having an average particle size of 2 to 6 μm are kneaded at a ratio of 100: 50 to 80% by weight. An injection-molded article for automobiles, comprising preparing a pelletized master batch, charging these two types of resin bodies into a hopper 6 of an injection molding machine 5 and performing injection molding while heating and melting. We propose a manufacturing method.
The mixing ratio of the first polymer and the second polymer is 60 to
It is good to set to 90:10 to 40% by weight. In general, talc is preferably used for the filler, and its particle size is preferably set to an average particle size of 2 to 6 μm. Bare particle size 2μm
Below, the dispersion of the filler is not sufficient, and when it is 6 μm or more, the mechanical properties are reduced.
【0007】[0007]
【発明の実施の形態】以下、図面を参照して本発明の好
適な実施例を例示的に詳しく説明する。但しこの実施例
に記載されている構成部品の寸法、材質、形状、その相
対的配置等は特に特定的な記載がないかぎりは、この発
明の範囲をそれに限定する趣旨ではなく、単なる説明例
にすぎない。本発明を従来技術と比較しながら説明す
る。先ず、メルトフローレートが30g/10分(23
0℃、荷重:2.16Kgf)で且つプロピレン含有量
が90重量%の第3のエチレン−プロピレン重合体と、
メルトフローレートが10g/10分且つプロピレン含
有量が25重量%の第3のエチレン−プロピレン重合体
とを図1に示すような一軸の押出機1で混練して形成し
た第2のペレット状混練樹脂体(以下PPという)を射
出成形機5のホッパ6に投入し、該射出成形機5内で両
者を混合しながら加熱溶融して型7内に射出成形してド
アトリムを製造したものを従来技術2とする。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Preferred embodiments of the present invention will be illustratively described in detail below with reference to the drawings. However, the dimensions, materials, shapes, relative arrangements, and the like of the components described in this embodiment are not intended to limit the scope of the present invention unless otherwise specified, and are merely illustrative examples. Only. The present invention will be described in comparison with the prior art. First, the melt flow rate was 30 g / 10 min (23
A third ethylene-propylene polymer having a temperature of 0 ° C., a load of 2.16 Kgf) and a propylene content of 90% by weight;
Second pellet-shaped kneading formed by kneading a third ethylene-propylene polymer having a melt flow rate of 10 g / 10 min and a propylene content of 25% by weight with a single-screw extruder 1 as shown in FIG. Conventionally, a resin body (hereinafter referred to as PP) is put into a hopper 6 of an injection molding machine 5, heated and melted while mixing the two in the injection molding machine 5, and injection molded into a mold 7 to produce a door trim. Technology 2.
【0008】次に前記第二の混練樹脂体PPと平均粒径
2〜3μmのフィラを100:75重量%の割合で混練
してペレット状化したマスタ−バッチとを用意し、これ
らの2種の樹脂体を図3に示すような、射出成形機5の
ホッパ6内に投入して加熱溶融しながら射出成形してド
アトリムを製造したものを従来技術1とする。Next, a master batch prepared by kneading the second kneaded resin body PP and a filler having an average particle diameter of 2 to 3 μm at a ratio of 100: 75% by weight and preparing a pellet is prepared. As shown in FIG. 3, a door trim is manufactured by putting the resin body into a hopper 6 of an injection molding machine 5 and performing injection molding while heating and melting the resin body.
【0009】一方本発明においては、メルトフローレー
トが50〜100g/10分(230℃、荷重:2.1
6Kgf)で且つプロピレン含有量が80〜99重量%
の第1のエチレン−プロピレン重合体(以下PPaとい
う)と、メルトフローレートが1〜20g/10分且つ
プロピレン含有量が30〜60重量%の第2のエチレン
−プロピレン重合体(以下PPbという)とを図1に示
すように一軸の押出機1で混練して形成した第1のペレ
ット状混練樹脂体と、該第1の混練樹脂体と平均粒径2
〜3μmのフィラを100:75重量%の割合で混練し
てペレット状化したマスタ−バッチとを用意し、これら
の2種の樹脂体を射出成形機5のホッパ6内に投入して
加熱溶融しながら射出成形してドアトリムを製造したも
のを実施例とし、実施例1については、PPaとPPb
の比を80:20、実施例2については、PPaとPP
bの比を90:10、実施例3については、PPaとP
Pbの比を60:40に夫々設定した。On the other hand, in the present invention, the melt flow rate is 50 to 100 g / 10 minutes (230 ° C., load: 2.1
6 kgf) and the propylene content is 80 to 99% by weight.
A first ethylene-propylene polymer (hereinafter referred to as PPa) and a second ethylene-propylene polymer (hereinafter referred to as PPb) having a melt flow rate of 1 to 20 g / 10 min and a propylene content of 30 to 60% by weight. As shown in FIG. 1, a first kneaded resin body formed by kneading with a single-screw extruder 1, a first kneaded resin body and an average particle diameter of 2
A master batch prepared by kneading a filler having a size of about 3 μm at a ratio of 100: 75% by weight and preparing a pellet is prepared, and these two types of resin bodies are put into a hopper 6 of an injection molding machine 5 and heated and melted. In this example, a door trim was manufactured by injection molding while performing injection molding. In Example 1, PPa and PPb were used.
Is 80:20, and in Example 2, PPa and PP
b: 90:10, and for Example 3, PPa and P
The ratio of Pb was set to 60:40, respectively.
【0010】又比較例してPPaとPPbの比を80:
20に設定した第1のペレット状混練樹脂体と、前記従
来技術に用いた第2の混練樹脂体(PP)と平均粒径2
〜3μmのフィラを100:75重量%の割合で混練し
てペレット状化したマスタ−バッチとを用意し、これら
の2種の樹脂体を射出成形機5のホッパ6内に投入して
加熱溶融しながら射出成形してドアトリムを製造したも
のを用いた。As a comparative example, the ratio of PPa to PPb is 80:
The first kneaded resin body set to 20 and the second kneaded resin body (PP) used in the prior art were mixed with an average particle size of 2
A master batch prepared by kneading a filler having a size of about 3 μm at a ratio of 100: 75% by weight and preparing a pellet is prepared, and these two types of resin bodies are put into a hopper 6 of an injection molding machine 5 and heated and melted. While the door trim was manufactured by injection molding, the product was used.
【0011】そして前記従来技術1,2、実施例1〜3
及び比較例について夫々比重、アイゾット衝撃値(KJ
/m2 )、熱変形温度H.D.T(℃)、曲げ弾性率
(MPa)を夫々調べてみた。その結果を図4に示す。The prior arts 1 and 2 and the first to third embodiments.
Specific gravity and Izod impact value (KJ
/ M 2 ), heat distortion temperature H.I. D. T (° C.) and flexural modulus (MPa) were examined. FIG. 4 shows the results.
【0012】先ずフィラが入っていない従来技術2につ
いては、アイゾット衝撃値(KJ/m2 )、熱変形温度
H.D.T(℃)、曲げ弾性率(MPa)のいずれも好
ましい数値を示すが、フィラが入っていないために、成
形品に光沢性がなく、好ましい外観品質を得られなかっ
た。First, for the prior art 2 having no filler, the Izod impact value (KJ / m 2 ), the heat distortion temperature D. Although both T (° C.) and flexural modulus (MPa) show preferable numerical values, the molded product has no gloss and no favorable appearance quality was obtained because no filler was contained.
【0013】又、従来技術1については、フィラが入っ
ているために、好ましい外観品質が得られたが、アイゾ
ット衝撃値が17(KJ/m2 )と従来技術2(17
(KJ/m2 ))に比較して大幅に低下している。これ
は前記従来技術に用いた第2の混練樹脂体(PP)を用
いてマスターバッチを構成した比較例1も同様であり、
アイゾット衝撃値も20(KJ/m2 )、熱変形温度も
126(℃)と従来技術1と同様に低下している。[0013] In addition, the prior art 1 provided good appearance quality due to the inclusion of the filler, but the Izod impact value was 17 (KJ / m 2 ), which was the same as that of the prior art 2 (17).
(KJ / m 2 )). This is the same in Comparative Example 1 in which a masterbatch is formed by using the second kneaded resin body (PP) used in the conventional technique,
The Izod impact value is also 20 (KJ / m 2 ), and the thermal deformation temperature is also 126 (° C.), which is lower as in the prior art 1.
【0014】一方、実施例1〜3についてはアイゾット
衝撃値が23〜27(KJ/m2 )、熱変形温度が12
8〜134(℃)、曲げ弾性率が1800〜1910
(MPa) といずれもフィラをいれない従来技術2と
ほぼ同様な物性値を得ることが出来た。尚、前記第1の
重合体と第2の重合体の配合比は60〜90:10〜4
0重量%に設定するのがよい。又フィラには一般にタル
クを用いるのがよく、その粒径は平均粒径2〜6μmに
設定するのがよい。けだし粒径が2μm以下ではフィラ
の分散が十分いかず、又6μm以上では機械的物性値が
低下する。On the other hand, in Examples 1 to 3, the Izod impact value was 23 to 27 (KJ / m 2 ) and the heat deformation temperature was 12
8-134 (° C), flexural modulus 1800-1910
(MPa) and the same physical property values as in the prior art 2 in which no filler was added. The mixing ratio of the first polymer and the second polymer is 60 to 90:10 to 4
It is good to set to 0% by weight. In general, talc is preferably used for the filler, and its particle size is preferably set to an average particle size of 2 to 6 μm. When the particle size is less than 2 μm, the filler is not sufficiently dispersed, and when the particle size is more than 6 μm, the mechanical properties decrease.
【0015】次に前記実施例1について、第1の混練樹
脂体と混練するフィラの粒径を2〜10の間で変化させ
たマスタ−バッチを夫々用意し、前記第1の混練樹脂体
とこれらのマスタ−バッチを夫々樹脂体を射出成形機5
のホッパ6内に投入して加熱溶融しながら射出成形して
ドアトリムを製造したものについてアイゾット衝撃値を
測定し、その結果を図5に示すようにフィラの粒径を横
軸とするグラフにまとめてみた。又本図より明らかな如
く、6μm以上では機械的物性値が低下することが理解
出来、又粒径が2μm以下ではフィラの分散が十分いか
ないことも理解出来た。Next, in the first embodiment, master batches in which the particle diameter of the filler to be kneaded with the first kneaded resin body was changed between 2 and 10 were prepared, and the first kneaded resin body and the master batch were prepared. Each of these master batches is molded into a resin body by an injection molding machine 5.
The Izod impact value was measured for a door trim manufactured by injection molding while being heated and melted in the hopper 6, and the results are summarized in a graph with the filler particle diameter as the horizontal axis as shown in FIG. I tried. Further, as is apparent from this figure, it was understood that the mechanical properties decreased when the particle diameter was 6 μm or more, and that the filler was not sufficiently dispersed when the particle diameter was 2 μm or less.
【0016】[0016]
【発明の効果】以上記載のごとく本発明によれば、大型
の押出機を用いることなく又製造工程の煩雑化を避けつ
つ充分な機械的物性値、特に低温衝撃値を向上させたド
アトリム、ピラートリム等の自動車用射出成形品の製造
方法を得ることが出来る。As described above, according to the present invention, door trims and pillar trims having sufficient mechanical properties, particularly low-temperature impact values, without using a large-sized extruder and avoiding complicated production steps. And the like can be obtained.
【図1】本発明が適用される押出/射出製造工程を示す
概略図である。FIG. 1 is a schematic view showing an extrusion / injection manufacturing process to which the present invention is applied.
【図2】第1の従来技術が適用される押出/射出製造工
程を示す概略図である。FIG. 2 is a schematic view showing an extrusion / injection manufacturing process to which a first prior art is applied.
【図3】第2の従来技術が適用される押出/射出製造工
程を示す概略図である。FIG. 3 is a schematic view showing an extrusion / injection manufacturing process to which a second prior art is applied.
【図4】前記従来技術1,2、実施例1〜3及び比較例
について夫々比重、アイゾット衝撃値(KJ/m2 )、
熱変形温度H.D.T(℃)、曲げ弾性率(MPa)を
夫々調べた結果を示す表図である。FIG. 4 shows specific gravity, Izod impact value (KJ / m 2 ) for the prior arts 1 and 2, Examples 1 to 3 and Comparative Example, respectively.
Heat deformation temperature H. D. It is a table | surface figure which shows the result of having investigated T (degreeC) and bending elastic modulus (MPa), respectively.
【図5】アイゾット衝撃値とフィラの粒径との関係を示
すグラフ図である。FIG. 5 is a graph showing a relationship between an Izod impact value and a filler particle size.
1、10 押出成形機 5 射出成形機 1,10 Extrusion molding machine 5 Injection molding machine
Claims (2)
10分(230℃、荷重:2.16Kgf)で且つプロ
ピレン含有量が80〜99重量%の第1のエチレン−プ
ロピレン重合体と、メルトフローレートが1〜20g/
10分且つプロピレン含有量が30〜60重量%の第2
のエチレン−プロピレン重合体とを押出機で混練して形
成したペレット状混練樹脂体と、該混練樹脂体と平均粒
径2〜6μmのフィラを100:50〜80重量%の割
合で混練してペレット状化したマスタ−バッチとを用意
し、これらの2種の樹脂体を射出成形機のホッパ内に投
入して加熱溶融しながら射出成形を行なうことを特徴と
する自動車用射出成形品の製造方法。1. A melt flow rate of 50 to 100 g /
A first ethylene-propylene polymer having a propylene content of 10 to 20 minutes (230 ° C., load: 2.16 Kgf) and a propylene content of 80 to 99% by weight, and a melt flow rate of 1 to 20 g /
10 minutes and the second having a propylene content of 30 to 60% by weight.
A kneaded resin body formed by kneading an ethylene-propylene polymer with an extruder and a filler having an average particle size of 2 to 6 μm are kneaded at a ratio of 100: 50 to 80% by weight. A pelletized master batch is prepared, and these two types of resin bodies are put into a hopper of an injection molding machine, and injection molding is performed while heating and melting. Method.
比を60〜90:10〜40重量%に設定したことを特
徴とする請求項1記載の自動車用射出成形品の製造方
法。2. The production of an injection molded article for an automobile according to claim 1, wherein the compounding ratio of the first polymer and the second polymer is set in a range of 60 to 90:10 to 40% by weight. Method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2921398A JPH11207772A (en) | 1998-01-27 | 1998-01-27 | Manufacture of automobile injection molded product |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2921398A JPH11207772A (en) | 1998-01-27 | 1998-01-27 | Manufacture of automobile injection molded product |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH11207772A true JPH11207772A (en) | 1999-08-03 |
Family
ID=12269925
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2921398A Pending JPH11207772A (en) | 1998-01-27 | 1998-01-27 | Manufacture of automobile injection molded product |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH11207772A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6660797B1 (en) | 1999-11-11 | 2003-12-09 | Japan Polychem Corporation | Propylene resin composition and method for molding the same |
-
1998
- 1998-01-27 JP JP2921398A patent/JPH11207772A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6660797B1 (en) | 1999-11-11 | 2003-12-09 | Japan Polychem Corporation | Propylene resin composition and method for molding the same |
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