JPS6258292B2 - - Google Patents
Info
- Publication number
- JPS6258292B2 JPS6258292B2 JP11178080A JP11178080A JPS6258292B2 JP S6258292 B2 JPS6258292 B2 JP S6258292B2 JP 11178080 A JP11178080 A JP 11178080A JP 11178080 A JP11178080 A JP 11178080A JP S6258292 B2 JPS6258292 B2 JP S6258292B2
- Authority
- JP
- Japan
- Prior art keywords
- thermoplastic resin
- resin
- mold
- filler
- component according
- 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.)
- Expired
Links
- 229920005992 thermoplastic resin Polymers 0.000 claims description 23
- 229920005989 resin Polymers 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 21
- 239000003365 glass fiber Substances 0.000 claims description 18
- 238000001746 injection moulding Methods 0.000 claims description 16
- 239000000945 filler Substances 0.000 claims description 12
- 238000002347 injection Methods 0.000 claims description 11
- 239000007924 injection Substances 0.000 claims description 11
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 10
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 6
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 3
- 229920001893 acrylonitrile styrene Polymers 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 3
- 239000011256 inorganic filler Substances 0.000 claims description 3
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 3
- 229910010272 inorganic material Inorganic materials 0.000 claims description 3
- 239000011147 inorganic material Substances 0.000 claims description 3
- 229920001955 polyphenylene ether Polymers 0.000 claims description 3
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 239000011324 bead Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 229920002223 polystyrene Polymers 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 description 7
- 230000006698 induction Effects 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- -1 polyoxymethylene Polymers 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 239000010410 layer Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- FGDAXMHZSNXUFJ-UHFFFAOYSA-N ethene;prop-1-ene;prop-2-enenitrile Chemical group C=C.CC=C.C=CC#N FGDAXMHZSNXUFJ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 229920001890 Novodur Polymers 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- WWNGFHNQODFIEX-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate;styrene Chemical compound C=CC=C.COC(=O)C(C)=C.C=CC1=CC=CC=C1 WWNGFHNQODFIEX-UHFFFAOYSA-N 0.000 description 1
- QSMOHLASMMAGIB-UHFFFAOYSA-N butyl prop-2-enoate;prop-2-enenitrile Chemical compound C=CC#N.CCCCOC(=O)C=C QSMOHLASMMAGIB-UHFFFAOYSA-N 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000012966 insertion method Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Vehicle Waterproofing, Decoration, And Sanitation Devices (AREA)
- Rear-View Mirror Devices That Are Mounted On The Exterior Of The Vehicle (AREA)
- Laminated Bodies (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
Description
本発明は充填材を含有する熱可塑性樹脂で射出
成形した車両部品であつて外観が良好なものに関
する。
熱可塑性樹脂は、成形加工が容易であること、
複雑な形状のものも簡単に成形可能であること、
さらに、同一形状物が大量生産可能であることと
いう一般的特性を有する。ことに車両部品として
は、重量軽減による車両の燃費効率の向上、およ
び耐食性の向上(さびない)等の特性が得られる
ので多くの部品が熱可塑性樹脂化されて来た。
一方、熱可塑性樹脂製車両部品として次の特性
が改善されると更に熱可塑性樹脂化が促進され、
車両の性能が向上することが期待される。
(イ) 強度、剛性の向上。
(ロ) 耐熱性の向上。
(ハ) 寸法安定性の向上。
(ニ) 車両部品特有の耐振動性の向上。
充填材入り熱可塑性樹脂は、上記(イ)〜(ニ)をそれ
ぞれ果しており、好ましい車両部品用材料である
が、充填材が熱可塑性がないため、および充填材
と熱可塑性樹脂との相溶性が悪いため、各々の材
料間に空隙ができるためか、射出成形した場合表
面が荒れ外観が悪く実用化されていない。インス
トウルメントパネル等では塗装することにより一
部実用化されている例はあるが、コスト高であ
り、また塗料中の一部成分(たとえばシンナー)
が樹脂を溶かすため耐衝撃性等の特性が低下する
ものであつた。
従つて本発明の目的は、このような外観上の問
題がなく塗装などせずにそのまま使用できる充填
材入り熱可塑性樹脂射出成形車両部品を提供する
にある。
すなわち本発明は、外観の良好さを必要とする
充填材入り熱可塑性樹脂射出成形車両部品におい
て、前記熱可塑性樹脂をHDT(ヒートデイスト
ーシヨンテンペラチユア加熱変形温度、JIS
K6871)80℃以上の熱可塑性樹脂とすると共に、
実質的に充填材を含まない前記熱可塑性樹脂の表
皮層を形成せしめたことを特徴とする車両部品に
ある。
以下添付図面に例示した本発明の好適な実施例
について詳述する。
第1図および第2図に射出成形装置を示す。こ
の例はインダクター挿入方式を示すものであつ
て、合成樹脂を溶融して射出を行なう射出シリン
ダー部分3と、固定側金型4と、移動側金型5と
により構成される射出成形機および高周波発振装
置1とこれに接続されて金型表面近傍に配置され
るインダクター2とより成る高周波誘導加熱桟に
より構成される。
射出成形せしめる熱可塑性合成樹脂は、たとえ
ばアクリロニトリル−スチレン共重合体(AS樹
脂)、アクリロニトリル−ブタジエン−スチレン
共重合体、アクリロニトリル−ブタジエン−スチ
レン−α−メチルスチレン、アクリロニトリル−
メチルメタクリレート−ブタジエン−スチレン、
アクリロニトリル−エチレン・プロピレンゴム−
スチレン共重合体、アクリロニトリル−アクリル
酸ブチルゴム−スチレン共重合体(ABS樹脂と
総称)ポリスチレン、ポリフエニレンエーテル、
ポリアミド、ポリオキシメチレン、ポリカーボネ
ート、ポリエチレン、ポリプロピレン、ポリブチ
レンテレフタレートなどのHDT80℃以上の熱可
塑性樹脂とする。このうち特に好ましいのは、
AS樹脂、ABS樹脂等のスチレン系樹脂及びPPE
樹脂である。またこれに混入する充填材としては
径5〜20μのガラス繊維を5〜40重量%好ましく
は15〜30重量%とする。さらに別な充填材とし
て、CaCO3、ガラスビーズ等の無機物および
Ee,Fe2O3,Al,Zno等の金属および合金および
それらの酸化物があげられる。このような無機物
の平均粒径は1〜100μ、また無機物充填材量は
20〜80重量%とする。
このような材料を射出成形するのであるが、こ
の際第2図の拡大断面図に示すように、固定側金
型4と移動側金型5の中間に高周波誘導加熱のイ
ンダクター2を設置する。移動側金型5と固定側
金型4との間にインダクター2をはさみこみ、は
さみこまれた状態で高周波を発振させると、第3
図に示すように金型表面(A点やB点)のみ急激
に温度が上昇し、金型内部(C点やD点)の温度
は高周波誘導加熱によつては温度上昇がほとんど
ない。第3図の例の場合は金型の冷却水による冷
却は行なつておらず、単純に高周波誘導加熱によ
る金型の温度分布の経時変化の例を示したもので
ある。しかるのちに金型4,5を一度開き、イン
ダクター2を固定側及び移動側金型4,5の間よ
り抜き出し再度金型を閉じ通常の射出成形と同じ
要領で上述の充填材入り熱可塑性樹脂の射出成形
を行なう。このようにして得た射出成形品の厚さ
方向の切断面の光学顕微鏡観察写生図を第4図に
示す。倍率は440倍である。参考のため同一金型
でインダクター2を使用せず金型温度60℃で同材
料を射出成形し、同断面を同様に観察写生したも
のが第5図である。倍率は440倍である。いずれ
の図面も島模様部はガラス繊維であり、横一線の
ラインは成形品表面である。
第4図と第5図とを比較しても明らかな様に本
発明になる成形品の場合充填材ガラス繊維A′が
成形品表面に現出することはなく少なくても1〜
30μの熱可塑性樹脂B′層が成形品表層部に形成さ
れている事がわかる。また、第4図に示す様にガ
ラス繊維A′が成形品表面に比較的近い位置に有
する時も熱可塑性樹脂B′層が表層に若干の凸凹を
形成しても第5図の場合と比較しなだらかな凸凹
を示すため光沢のある外観を有する成形品を得
る。一方通常の成形品の場合第5図に示す様にガ
ラス繊維A′が成形表面に突き出ていたり、また
ガラス繊維A′が表層近くにある場合即ち金型表
面での樹脂の流れが疎外されるためか表面にシル
バーストリーク状の凸凹が出来、いわゆる光沢の
ないガサガサした表面の成形品しか得ることはで
きない。本発明になる成形品の外観の良さ、光沢
度を定量化するためASTM D523により成形品の
光沢度Gs(60゜)を測定した結果98%であつ
た。一方金型温度60℃の成形品は光沢度45%であ
り本発明になる成形品外観の平滑性、光沢の良さ
を示している。また本発明になる成形品は射出成
形時の流動抵抗が少なく配向歪が発生しずらいた
めかJIS K6871に規定された加熱変形温度を測定
したところ通常の成形品に比較し加熱変形温度が
3〜5℃向上し、いわゆる実用耐熱温度が向上す
る事、成形品の落下強さ等比較した結果実用タフ
ネスも向上する。
実施例 1
ガラス繊維20重量%を添加したAES樹脂(ア
クリロニトリル−エチレン・プロピレンゴム−ス
チレン共重合体樹脂通称耐候性改良ABS樹脂)
を用いて、第6図に示す乗用車のフエンダーミラ
ーボデイを射出成形した。
金型はNAK材(超硬合金金型鋼)を利用し金
型の成形品形成面は鏡面仕上げにした。
インダクターは5mm径の鋼管を該金型鏡面仕上
げ部形状にそわせてほぼ渦巻に配置し該形状を固
定するため非磁性材である樹脂(エポキシ樹脂)
で注型し固化・作成した。
射出成形条件は該ガラス繊維強化AES樹脂の
温度が250℃になる様にシリンダー温度を設定し
た。該ガラス繊維強化AES樹脂を金型内に射出
する前に上述のインダクターを金型の間にはさみ
こみ7KHz、25KWの高周波発振器により15秒間発
振し、しかるのち金型を開きインダクターを金型
間より抜き出し、再度金型を閉じた。
なお本射出成形工程において、成形品を形成さ
せるべき鏡面仕上げにした金型表面は該樹脂を金
型内に射出する直前において該金型表面温度は高
周波誘導加熱により該金型表面付近のみを選択的
に加熱するため120℃〜130℃であるが該金型表面
より3〜5cm内部の金型温度は50〜60℃であつ
た。
しかるのち通常の射出成形と同様に上記金型内
に該樹脂を60Kg/cm2の射出圧で10秒間射出し冷却
時間40秒で成形品を取り出した。
全成形サイクルは75〜80秒であつた。
該フエンダーミラーボデイを使用しフエンダー
ミラーを組立て、振動テストした結果は第1表に
示す通り良好であり、また外観も非常に高光沢か
つ均一な光沢を有しガラス繊維強化熱可塑性樹脂
によくあつた、フローマーク、シルバーストリー
ク、ジエツテング等もないフエンダーミラーを
得、外観は塗装の必要もなく充分実用にたえるも
のであつた。
比較例 1
実施例1と同じ樹脂、同一金型、成形材、を使
用、高周波発振により金型表面を予熱する工程だ
けでなく他の成形条件が同じ場合のフエンダーミ
ラーの性能を同様に第1表に示す。
比較例 2
比較例1のガラス繊維強化AES樹脂の代りに
ガラス繊維強化されない即ちガラス繊維を添加し
ていないAES樹脂を使用した以外は全て比較例
1と同じ条件で作成したフエンダーミラーの性能
も同様に第1表に示す。
The present invention relates to a vehicle part injection molded from a thermoplastic resin containing a filler and having a good appearance. Thermoplastic resins are easy to mold and process;
Even complex shapes can be easily formed.
Furthermore, it has the general property that objects of the same shape can be mass-produced. In particular, many vehicle parts have been made of thermoplastic resins because they offer properties such as improved vehicle fuel efficiency due to weight reduction and improved corrosion resistance (no rust). On the other hand, if the following properties of thermoplastic resin vehicle parts are improved, the use of thermoplastic resin will be further promoted.
It is expected that vehicle performance will improve. (b) Improved strength and rigidity. (b) Improved heat resistance. (c) Improved dimensional stability. (d) Improving vibration resistance specific to vehicle parts. Filled thermoplastic resin fulfills each of (a) to (d) above and is a preferable material for vehicle parts, but the filler is not thermoplastic and the compatibility between the filler and thermoplastic resin is poor. Due to the poor quality, the surface is rough when injection molded, probably due to the formation of voids between each material, and the appearance is poor, so it has not been put to practical use. Although there are some examples of instrument panels being put into practical use by painting them, the cost is high, and some components of the paint (for example, thinner)
Since the resin melts, properties such as impact resistance deteriorate. Accordingly, an object of the present invention is to provide a filled thermoplastic resin injection molded vehicle part that does not have such problems in appearance and can be used as is without painting or the like. That is, the present invention provides thermoplastic resin injection-molded vehicle parts with fillers that require good appearance, in which the thermoplastic resin is heated to HDT (Heat Distortion Temperature, JIS
K6871) Thermoplastic resin with a temperature of 80℃ or higher,
The present invention provides a vehicle component characterized in that a skin layer of the thermoplastic resin is formed which substantially contains no filler. DESCRIPTION OF THE PREFERRED EMBODIMENTS Preferred embodiments of the present invention will be described in detail below as illustrated in the accompanying drawings. An injection molding apparatus is shown in FIGS. 1 and 2. This example shows an inductor insertion method, and includes an injection molding machine and a high-frequency It is constituted by a high frequency induction heating beam consisting of an oscillating device 1 and an inductor 2 connected to the oscillating device 1 and placed near the mold surface. Thermoplastic synthetic resins for injection molding include, for example, acrylonitrile-styrene copolymer (AS resin), acrylonitrile-butadiene-styrene copolymer, acrylonitrile-butadiene-styrene-α-methylstyrene, and acrylonitrile-styrene copolymer.
Methyl methacrylate-butadiene-styrene,
Acrylonitrile - ethylene propylene rubber -
Styrene copolymer, acrylonitrile-butyl acrylate rubber-styrene copolymer (generally referred to as ABS resin) polystyrene, polyphenylene ether,
Thermoplastic resins with an HDT of 80°C or higher, such as polyamide, polyoxymethylene, polycarbonate, polyethylene, polypropylene, and polybutylene terephthalate. Among these, particularly preferred are:
Styrenic resins such as AS resin, ABS resin, and PPE
It is resin. The filler to be mixed into this is 5 to 40% by weight, preferably 15 to 30% by weight of glass fibers having a diameter of 5 to 20μ. Further fillers include inorganic materials such as CaCO 3 , glass beads, and
Examples include metals and alloys such as Ee, Fe 2 O 3 , Al, and Zno, and their oxides. The average particle size of such inorganic materials is 1 to 100μ, and the amount of inorganic filler is
20 to 80% by weight. Such a material is injection molded, and at this time, as shown in the enlarged sectional view of FIG. 2, an inductor 2 for high-frequency induction heating is installed between the stationary mold 4 and the movable mold 5. When the inductor 2 is sandwiched between the movable mold 5 and the stationary mold 4 and a high frequency is oscillated in the sandwiched state, the third
As shown in the figure, only the temperature on the surface of the mold (points A and B) rises rapidly, and the temperature inside the mold (points C and D) hardly rises due to high-frequency induction heating. In the case of the example shown in FIG. 3, the mold is not cooled with cooling water, but simply shows an example of the change over time in the temperature distribution of the mold due to high-frequency induction heating. Thereafter, the molds 4 and 5 are opened once, the inductor 2 is extracted from between the fixed and movable molds 4 and 5, the mold is closed again, and the above-mentioned thermoplastic resin containing filler is injected in the same manner as normal injection molding. Performs injection molding. FIG. 4 shows an optical microscope observation sketch of the cut surface in the thickness direction of the injection molded product thus obtained. The magnification is 440x. For reference, the same material was injection molded using the same mold at a mold temperature of 60° C. without using the inductor 2, and the same cross section was similarly observed and sketched in FIG. 5. The magnification is 440x. In both drawings, the island pattern is made of glass fiber, and the horizontal line is the surface of the molded product. As is clear from comparing FIG. 4 and FIG. 5, in the case of the molded product of the present invention, the filler glass fibers A' do not appear on the surface of the molded product, and at least 1~
It can be seen that a 30μ thermoplastic resin B' layer is formed on the surface of the molded product. Also, as shown in Figure 4, when the glass fiber A' is located relatively close to the surface of the molded product, even if the thermoplastic resin B' layer forms some unevenness on the surface layer, compared to the case in Figure 5. A molded product having a glossy appearance due to its gentle unevenness is obtained. On the other hand, in the case of a normal molded product, as shown in Figure 5, if the glass fiber A' protrudes from the molding surface, or if the glass fiber A' is near the surface layer, the flow of resin on the mold surface will be hindered. Because of this, silver streak-like irregularities occur on the surface, and only molded products with so-called dull and rough surfaces can be obtained. In order to quantify the good appearance and gloss of the molded product of the present invention, the gloss Gs (60°) of the molded product was measured according to ASTM D523, and the result was 98%. On the other hand, the molded product produced at a mold temperature of 60°C had a gloss level of 45%, demonstrating the smoothness and gloss of the molded product appearance of the present invention. Also, perhaps because the molded product of the present invention has low flow resistance during injection molding and is less likely to cause orientation distortion, when the heat distortion temperature specified in JIS K6871 was measured, the heat distortion temperature was 3 to 3. The so-called practical heat resistance temperature is improved by 5°C, and as a result of comparing the drop strength of molded products, the practical toughness is also improved. Example 1 AES resin added with 20% by weight of glass fiber (acrylonitrile-ethylene propylene rubber-styrene copolymer resin commonly known as weather-resistant ABS resin)
The fender mirror body of a passenger car shown in FIG. 6 was injection molded using the same. The mold uses NAK material (carbide mold steel), and the molded product forming surface of the mold has a mirror finish. The inductor is made of a 5mm diameter steel tube that is arranged in a spiral shape to match the shape of the mirror-finished part of the mold, and is made of non-magnetic resin (epoxy resin) to fix the shape.
It was cast and solidified. As for the injection molding conditions, the cylinder temperature was set so that the temperature of the glass fiber reinforced AES resin was 250°C. Before injecting the glass fiber reinforced AES resin into the mold, the above-mentioned inductor was inserted between the molds and oscillated for 15 seconds using a 7KHz, 25KW high frequency oscillator, then the mold was opened and the inductor was extracted from between the molds. , and closed the mold again. In this injection molding process, the surface of the mirror-finished mold on which the molded product is to be formed is heated by high-frequency induction heating to select the surface temperature of the mold surface immediately before the resin is injected into the mold. Although the temperature was 120°C to 130°C to heat the mold, the temperature within 3 to 5 cm from the mold surface was 50 to 60°C. Thereafter, the resin was injected into the mold for 10 seconds at an injection pressure of 60 kg/cm 2 in the same manner as in ordinary injection molding, and the molded product was taken out after a cooling time of 40 seconds. The entire molding cycle was 75-80 seconds. A fender mirror was assembled using the fender mirror body, and the results of a vibration test were good as shown in Table 1, and the appearance was very high gloss and uniform, making it compatible with glass fiber reinforced thermoplastic resin. In addition, the fender mirror was free of flow marks, silver streaks, jet extensions, etc., and the exterior was fully usable without the need for painting. Comparative Example 1 The same resin, same mold, and molding material as in Example 1 were used, and the performance of the fender mirror was similarly evaluated in the first example when not only the process of preheating the mold surface by high-frequency oscillation but also other molding conditions were the same. Shown in the table. Comparative Example 2 The performance of a fender mirror made under the same conditions as Comparative Example 1 was also the same, except that instead of the glass fiber reinforced AES resin of Comparative Example 1, an AES resin that was not reinforced with glass fiber, that is, without glass fiber added, was used. are shown in Table 1.
【表】【table】
【表】
実施例 2
HDT85℃のABSにガラス繊維20%添加した樹
脂を用い、実施例1に記載した高周波誘導加熱に
より金型表面を加熱する方式の射出成形により、
巾6cm長さ1.2mの自動車フロントガラス部デフ
ロスターノズル付リツドを製作した。比較例とし
て同じ高周波誘導加熱による射出成形でHDT78
℃のABSにガラス繊維20%添加した樹脂を用い
て同様な成形品を得た。また、他の比較例として
従来の射出成形によつて、ガラス繊維無添加の
HDT90℃のABS樹脂、HDT78℃のABSにガラス
繊維20%添加した樹脂、およびHDT85℃のABS
にガラス繊維20%添加した樹脂の同じ成形品を作
つた。その性能試験結果を第2表に示す。[Table] Example 2 Using a resin with 20% glass fiber added to ABS with an HDT of 85°C, injection molding was carried out using the method described in Example 1 in which the mold surface was heated by high-frequency induction heating.
We manufactured a lid with a defroster nozzle for the windshield of an automobile that is 6 cm wide and 1.2 m long. As a comparative example, HDT78 was made by injection molding using the same high-frequency induction heating.
A similar molded product was obtained using a resin containing 20% glass fiber added to ABS at ℃. In addition, as another comparative example, by conventional injection molding, a glass fiber-free product was
ABS resin with HDT 90℃, resin with 20% glass fiber added to ABS with HDT 78℃, and ABS with HDT 85℃
The same molded product was made from a resin with 20% glass fiber added. The performance test results are shown in Table 2.
【表】
一般に、本発明による車両部品と従来の射出成
形車両部品との性能を第3表において比較して示
す。TABLE In general, the performance of vehicle parts according to the invention and conventional injection molded vehicle parts is compared in Table 3.
【表】
なお、ここで車両部品とは、具体的には自動車
部品におけるインストウルメント・パネル、フロ
ントエクステンシヨンパネル、ドアロツク、フロ
ントグリル、フエンダーミラーボデイ、ウインド
レギユレーターハンドル等であるが、これらに限
らず一般に自動車、モーターバイク、バス、トラ
ツク等の車両の部品を包含するものである。[Table] Vehicle parts here specifically include automobile parts such as instrument panels, front extension panels, door locks, front grilles, fender mirror bodies, and wind regulator handles. It generally includes parts for vehicles such as automobiles, motorbikes, buses, and trucks.
第1図は本発明部品の製造に用いるインダクタ
ーはさみこみ方式の射出成形機の概念的な側面
図、第2図はその金型とインダクターとの垂直断
面図、第3図は第1図および第2図に示した射出
成形機での金型の温度分布を示すグラフ、第4図
は本発明部品の切断面の拡大写生図、第5図は従
来部品の同様な図面、第6図は本発明を実施した
フエンダーミラーボデイの展開斜視図である。
1……高周波発振装置、2……インダクター、
3……射出シリンダー部分、4,5……金型。
Fig. 1 is a conceptual side view of an inductor insert type injection molding machine used for manufacturing parts of the present invention, Fig. 2 is a vertical cross-sectional view of the mold and inductor, and Fig. 3 is a cross-sectional view of the inductor insert type injection molding machine used for manufacturing parts of the present invention. A graph showing the temperature distribution of the mold in the injection molding machine shown in the figure, Figure 4 is an enlarged sketch of the cut surface of the part of the present invention, Figure 5 is a similar drawing of the conventional part, and Figure 6 is the figure of the present invention. FIG. 2 is an exploded perspective view of a fender mirror body that has undergone the above steps. 1... High frequency oscillator, 2... Inductor,
3... Injection cylinder part, 4, 5... Mold.
Claims (1)
性樹脂射出成形車両部品において、前記熱可塑性
樹脂をHDT 80℃以上の熱可塑性樹脂とすると共
に、表面光沢度(Gs(60゜)%/ASTMD523)
が80%以上、疲労限界(ASTMD671)が3.0Kg/
mm2以上好ましくは3.5Kg/mm2以上であり、かつ実
質的に充填材を含まない前記熱可塑性樹脂の表皮
層を接合界面を有さずに射出成形時に一体的に形
成せしめたことを特徴とする車両部品。 2 前記充填材が5〜20μ径のガラス繊維で、そ
の含有量が15〜30重量%である特許請求の範囲第
1項記載の車両部品。 3 前記充填材が平均粒径1〜100μの無機物充
填材で、その含有量が20〜80重量%である特許請
求の範囲第1項記載の車両部品。 4 前記無機物充填材がCaCO3、ガラスビーズ
等の無機物、Fe,Fe2O3,Al,ZnO等の金属及び
合金及びそれらの酸化物である特許請求の範囲第
3項記載の車両部品。 5 前記熱可塑性樹脂がポリスチレン、アクリロ
ニトリル−スチレン樹脂、アクリロニトリル−ブ
タジエン−スチレン系樹脂等のスチレン系樹脂で
ある特許請求の範囲第1項記載の車両部品。 6 前記熱可塑性樹脂がポリフエニレンエーテル
である特許請求の範囲第1項記載の車両部品。[Claims] 1. In a filled thermoplastic resin injection molded vehicle part that requires good appearance, the thermoplastic resin is a thermoplastic resin with an HDT of 80°C or higher, and the surface glossiness (Gs ( 60゜)%/ASTMD523)
is more than 80%, fatigue limit (ASTMD671) is 3.0Kg/
mm 2 or more, preferably 3.5 Kg/mm 2 or more, and the skin layer of the thermoplastic resin containing substantially no filler is integrally formed during injection molding without a bonding interface. and vehicle parts. 2. The vehicle component according to claim 1, wherein the filler is glass fiber with a diameter of 5 to 20 μm, and the content thereof is 15 to 30% by weight. 3. The vehicle component according to claim 1, wherein the filler is an inorganic filler with an average particle size of 1 to 100 μm, and the content thereof is 20 to 80% by weight. 4. The vehicle component according to claim 3, wherein the inorganic filler is an inorganic material such as CaCO 3 or glass beads, a metal or alloy such as Fe, Fe 2 O 3 , Al, or ZnO, or an oxide thereof. 5. The vehicle component according to claim 1, wherein the thermoplastic resin is a styrene resin such as polystyrene, acrylonitrile-styrene resin, or acrylonitrile-butadiene-styrene resin. 6. The vehicle component according to claim 1, wherein the thermoplastic resin is polyphenylene ether.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11178080A JPS5736655A (en) | 1980-08-15 | 1980-08-15 | SHARYOBUHIN |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11178080A JPS5736655A (en) | 1980-08-15 | 1980-08-15 | SHARYOBUHIN |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5736655A JPS5736655A (en) | 1982-02-27 |
| JPS6258292B2 true JPS6258292B2 (en) | 1987-12-04 |
Family
ID=14569971
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11178080A Granted JPS5736655A (en) | 1980-08-15 | 1980-08-15 | SHARYOBUHIN |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5736655A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06351B2 (en) * | 1988-04-08 | 1994-01-05 | 静岡県 | Inorganic filler Highly filled thermoplastic resin molding manufacturing method |
-
1980
- 1980-08-15 JP JP11178080A patent/JPS5736655A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5736655A (en) | 1982-02-27 |
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