JPS6159212B2 - - Google Patents
Info
- Publication number
- JPS6159212B2 JPS6159212B2 JP7124580A JP7124580A JPS6159212B2 JP S6159212 B2 JPS6159212 B2 JP S6159212B2 JP 7124580 A JP7124580 A JP 7124580A JP 7124580 A JP7124580 A JP 7124580A JP S6159212 B2 JPS6159212 B2 JP S6159212B2
- Authority
- JP
- Japan
- Prior art keywords
- mold
- molded
- surface layer
- base material
- product
- 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
- 239000002344 surface layer Substances 0.000 claims description 84
- 239000000463 material Substances 0.000 claims description 68
- 229920003002 synthetic resin Polymers 0.000 claims description 42
- 239000000057 synthetic resin Substances 0.000 claims description 42
- 229910052751 metal Inorganic materials 0.000 claims description 37
- 239000002184 metal Substances 0.000 claims description 37
- 239000010410 layer Substances 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 26
- 239000000945 filler Substances 0.000 claims description 20
- 238000000465 moulding Methods 0.000 claims description 17
- 229920001169 thermoplastic Polymers 0.000 claims description 12
- 239000004416 thermosoftening plastic Substances 0.000 claims description 12
- 238000002844 melting Methods 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 10
- 239000003365 glass fiber Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000004381 surface treatment Methods 0.000 claims description 7
- 238000003486 chemical etching Methods 0.000 claims description 4
- 238000007796 conventional method Methods 0.000 claims description 3
- 238000005304 joining Methods 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims description 2
- 238000002347 injection Methods 0.000 description 29
- 239000007924 injection Substances 0.000 description 29
- 238000001746 injection moulding Methods 0.000 description 20
- 239000005445 natural material Substances 0.000 description 15
- 229920005668 polycarbonate resin Polymers 0.000 description 12
- 239000004431 polycarbonate resin Substances 0.000 description 12
- 238000007747 plating Methods 0.000 description 11
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 239000000835 fiber Substances 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- -1 polypropylene Polymers 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 239000003929 acidic solution Substances 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 229920001230 polyarylate Polymers 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 229920006351 engineering plastic Polymers 0.000 description 3
- 238000005530 etching Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 2
- 208000014451 palmoplantar keratoderma and congenital alopecia 2 Diseases 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000001119 stannous chloride Substances 0.000 description 2
- 235000011150 stannous chloride Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007772 electroless plating Methods 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 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
- 239000003350 kerosene Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001291 polyvinyl halide Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910001432 tin ion Inorganic materials 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 238000007666 vacuum forming Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Injection Moulding Of Plastics Or The Like (AREA)
- Chemically Coating (AREA)
Description
本発明はガラス繊維、無機物粉末等の充填材に
より補強された熱可塑性合成樹脂製品の表層に高
光択を与えた製品の製造方法に関する。
ガラス繊維、無機物粉末等の充填材を混入した
合成樹脂製品は、充填材の混入により高強度、耐
熱、耐摩耗性等の特性が得られることから、製品
の使用目的に環境に適応させ、かつ使用合成樹脂
の材質と組合わせて、広く使用されている。特に
自動車業界、家庭電化製品業界等においては、そ
の軽量であることと加工性が良好であることを利
用して広く実用化され、一般にエンジニアリン
グ・プラスチツクスと呼ばれている。しかしなが
ら、エンジニアリング・プラスチツクスには、ポ
リメチルメタクリレート、エポキシ、ポリフエニ
レンオキシド、ポリカーボネート、ABS、ナイ
ロン、ポリアリレート、ポリプロピレン、ポリオ
キシメチレン、ポリブチレンテレフタレート、ポ
リスチレン、不飽和ポリエステル、ジアセテー
ト、トリアセテート、ユリア、メラミン、フエノ
ール等多くの単独または共重合体の樹脂の成形部
材から成るものがあり、その成形品は材質によつ
ては表面硬度や表面光沢が劣り、あるいは表面に
充填材であるガラス繊維や無機物等が現われ、こ
れを塗装や金属メツキ処理によつて補うことが行
われているが、表面光沢の良好な製品を得るには
極めて多くの工数を必要とする欠点があつた。ま
た充填材混入の樹脂製品の表面に直接メツキ等の
金属被覆膜を形成した場合に、化学腐蝕液による
処理の際に充填材の繊維または粉末が表面に突出
し、メツキ肌に凹凸を生ぜしめ、光沢を悪くする
とともに外観に美観を失わせてしまう。この凹凸
を修復するには肉厚のメツキ膜をつけることも考
えられるが徒らに手数を要し工業生産には適さな
い。
本発明は、上記事実に鑑み、合成樹脂製品の基
体をガラス繊維、無機物粉末等の充填材を混入し
た熱可塑性合成樹脂により成形体を形成せしめて
その製品の強度、剛性、耐摩耗性等の諸性質を改
善するとともに、該製品の表面の一部または全部
に前記充填材を混入しない熱可塑性合成樹脂の表
層を層着せしめ、該表層に光沢度の良い表面を形
成せしめ、さらに前記表層の表面に金属表面処理
を施して光輝度の高い金属皮膜層を形成した合成
樹脂製品であつて、長年使用しても金属皮膜層に
フクレ、剥離、割れ等の外観上の欠陥の発生する
おそれの極めて少い製品を提供することを目的と
する合成樹脂製品の製造方法であつて、その特徴
とするところは、前記製品の基材または表層の何
れか一方を先ず成形して金型の型面に装着する第
1工程と、次に前記基材または表層のうちの他方
を溶融し、前記金型の型空間に充填、成形し、先
に金型の型面に装着した前記一方の成形体の表面
を軟化ないし溶融させつつ後に充填成形した成形
体とその接触部において混合成層を形成せしめ、
基材と表層の二層を両者の接触部に混合成層を形
成せしめて一体に接合層着せしめる第2工程と、
前記基材および表層の層着成形体を前記金型より
とり出し、前記表層の表面を常法により化学腐食
液で処理した後金属表面処理を施して金属皮膜層
を形成する第3工程とから成る合成樹脂製品の製
造方法に係る。
さらに本発明において好ましくは、前記基材ま
たは表層の何れか一方の成形体は、前記金型の型
空間内において所定の型面を利用しかつ該成形体
を形成する第2の金型を用いて予め溶融、充填せ
しめられて成形され、前記基材または表層の他方
は、先に金型に充填成形された一方の成形体が溶
融ないし未硬化の状態にある間に、前記第1の金
型と第3の金型とで形成された製品形状の型空間
内に他方の成形体を形成すべき合成樹脂を溶融、
充填せしめ、基材および表層の接触部に混合成層
を形成せしめて一体化せしめるものである。
本発明において使用する樹脂は前記エンジニア
リング・プラスチツクスに用いられる熱可塑性合
成樹脂はすべて使用できるが、前記基材と表層の
二層間を混合成層で一体化する相容性の良い好ま
しい樹脂は、ポリオレフイン、ポリアリレート、
ポリメタアクリレート、ポリスチレン、ポリハロ
ゲン化ビニール、ポリアミド、ポリエステル、ポ
リカーボネート、ポリアクリルニトリル等の単独
あるいは共重合体である。
また充填材としてはガラス繊維、石綿、炭素繊
維等の無機質繊維およびビニロン繊維等の有機繊
維、ならびに金属粉末、炭素粉末、グラフアイト
粉末等の無機物粉末が使用できるが、一般的には
無機質繊維が好ましい。充填材用繊維は、その長
さが長いと溶融された合成樹脂の流れが悪く、緻
密な型面を形成した金型での成形加工はむつかし
くなり、その太さが太く、長さが短かければ製品
を補強する効果が少く、製品をもろくする要因と
もなる。自動車部品等の機能部品においても使用
される部品の性格によつて差はあるが、装飾的な
部品では繊維長は0.4〜4mm、線径1.0〜10-4mm、
断面積0.8〜8×10-7mm2の単繊維が好ましい。
そして上記充填材は予め合成樹脂と混練して形
状をコンパウンド状あるいはチツプ状に予め成形
しておき、射出成形機により成形せしめられる。
本発明を、第1の金型に第2および第3の金型
を組合せ、二重の射出成形を行う実施方法に基い
て説明する。
第1図は上記方法に使用する射出成形機の概要
を示すものであつて、基台1には、該基台1に適
宜方法により支承杆2,2によつて固定されてい
る固定板3と可動板4とが対向せしめられて配設
され、該可動板4は前記支承杆2,2によつて固
定板3に向つてまたは固定板3から離反する方向
に向けて往復動せしめられる可動フレーム5に支
軸6により回転可能に支承せしめられている。
可動板4には、所望の樹脂製品の一面を形成す
べき型面7,7を刻設した第1の金型8,8が2
個、支軸6の中心から等しい距離で180度の回転
角位置に固定され、一方固定板3には第2の金型
9および第3の金型10が前記可動板4の回転中
心に関し等しい距離で180度の回転角位置で、か
つ可動板4が支承杆2,2により摺動前進せしめ
られた際前記第1の金型8,8にそれぞれ同時に
結合せしめられる関係位置に固定されている。前
記第2の金型9には、該金型9が第1の金型8と
結合せしめられたとき第1の金型8の型面7とと
もに所望製品の表層を成形すべき型面11が刻設
せられており、前記第3の金型10には、該金型
10が第1の金型8と結合せしめられたとき第1
の金型8の型面7とともに所望製品の形状を成形
すべき型面12が刻設せられている。固定板3に
は、前記第2の金型9の型面11に開口する孔1
3に射出シリンダ14が開口するよう固定され、
金型9とともに第1の射出成形ステーシヨン15
を構成しており、さらに前記第3の金型10の型
面12に開口する孔16に射出シリンダ17が開
口するように固定され第2の射出ステーシヨン1
8を構成している。
本発明を前記第1図の射出成形機を用いて実施
する態様は次のとおりである。
金型8,9,10を十分に加熱しておき、可動
板4を可動フレーム5により前進せしめ、第1の
金型8,8にそれぞれ第2の金型9、第3の金型
10を結合せしめる。先ず第1の射出ステーシヨ
ン15において、充填材を混合しない熱可塑性合
成樹脂(ナチユラル材)を溶融状態で射出シリン
ダ14から孔13を介して圧入、充填し、型面
7,11間の型空間で所望製品の表層50を成形
する。
次に該表層50を形成する合成樹脂の表面がや
や冷却してその形状を保つてはいるが内部は溶融
している状態ないし該表層50が未硬化の軟かい
状態の間に可動板4を後退させ、その回転中心を
中心として180度回転させて再び前進せしめる
と、前記表層50を型面7に装着した第1の金型
8は第2射出ステーシヨン18において第3の金
型10と結合される。第3の金型10の型面12
は金型8の型面7とともに所望製品の形状の型空
間を形成するから、第2の射出ステーシヨン18
において充填材を混入した熱可塑性合成樹脂
(FRTP)を溶融せしめ、射出シリンダ17、孔
16を介して前記型空間に圧入、充填せしめる
と、FRTPは前記ナチユラル材の表層50と第3
の金型10の型面12との間で基材60に成形さ
れ、かつ、前記ナチユラル材の表層50は未だ高
温であるため圧入充填されたFRTP基材60との
接触面で溶融状態となつて両者が一体化されるの
で、金型8,10内で冷却後製品をとり出すと、
ナチユラル材の表層50とFRTPの基材60はそ
の両者の接触面が混合成層で一体化され、層着さ
れた製品を得る。この製品の表層50は充填材を
含まないナチユラル材であるため型面7の表面仕
上げ度に適応した光沢のある表面を呈し、基材6
0は充填材の混合されたFRTPであるため高強
度、靭性、耐熱性、耐久性を具備し、かつ表層5
0と基材60の接合面は混合成層で一体化され、
その接着力は極めて強固である。本発明における
表層50の成形は製品の表面に光沢を与え外観美
を具備せしめるものであるから、自動車部品のよ
うな機能製品にあつても0.2〜1.5mm程度が適当で
ある。
なお本発明の実施にあたり、第1の金型8の型
面7をFRTPによる基材60を成形すべき型面と
し、第1の射出ステーシヨン15において先に基
材60を成形し、次いで第2の射出ステーシヨン
18の型面12を表層50の表面を成形すべき型
面とし、第2の射出ステーシヨン18において表
層50を射出成形して基材60と一体化せしめる
こともできる。
この二重射出成形機を利用する方法において
は、第1の射出ステーシヨン15において表層5
0または基材60の何れか一方を射出成形により
成形した後、可動板4を後退せしめ、180度の回
転を行い、再び前進せしめて、第2の射出ステー
シヨン18において他方の射出成形が行われるの
で、第1の射出ステーシヨン15における成形と
第2の射出ステーシヨン18における成形との間
の移動時間を極めて短時間となし得るから、第1
の射出ステーシヨン15により成形された表層5
0または基材の何れか一方の成形体はその表面の
み成形されて内部が溶融している状態ないしは未
硬化の軟かい状態において第2の射出ステーシヨ
ン18によつて射出成形を受け、所望の製品とさ
れるので、表層50と基材60の接触面を混合成
層化することは極めて容易であり、第2の射出成
形ステーシヨン18における合成樹脂の溶融温度
を第1の射出ステーシヨン15における合成樹脂
の溶融温度より約10〜40℃、好ましくは20〜35℃
高温とすれば、通常の射出成形サイクルで表層5
0と基材60の密着度の良好な製品を得ることが
できる。
また本発明の前記実施方法からも理解されるよ
うに、本発明においては、表層50または基材6
0の何れか一方を予め成形しておき、その成形品
を射出成形機の型空間内に装着し、他方を形成す
べき合成樹脂を溶融せしめて射出成形する実施方
法を採用することもできる。
即ち第1図の符号を用いてこれを説明すれば、
第1の金型8および第2の金型9を使用し、ナチ
ユラル材を射出成形して、表層50を予め多数成
形しておく。次に第1の金型8および第3の金型
10を使用し、十分な高温に予熱された第1の金
型8の型面7に前記予め成形された表層50を装
着し、第3の金型10を第1の金型8に結合して
表層50と第3の金型10の型面12間にFRTP
を十分な高温に溶融せしめて射出成形するとき
は、金型8に装着された表層50の溶融FRTPに
接する面はその温度で溶融ないし軟化せしめら
れ、FRTPとナチユラル材の混合成層を形成して
基材60と一体化せしめられ、層着せしめること
ができる。この実施方法において予め基材60を
FRTPで成形しておき、射出成形機によりナチユ
ラル材を射出成形により基材60の一面に成形せ
しめて表層50を形成してもよいことは勿論であ
り、本実施方法においては予め成形する表層50
または基材60の一方は、後に成形される他方の
合成樹脂の射出時の温度において溶融されまたは
軟化される成分組織のものが好ましく、後に行わ
れる樹脂の充填圧力を十分に高くすることが好ま
しい。
本発明の他の特徴は、上記のようにFRTPの基
材60の表面の一部または全部に光沢度のよいナ
チユラル材の表層50を密着度良く層着せしめた
ものであるから、前記表層50の表面にプラスチ
ツクメタライジングにより金属表面処理を施すこ
とにより、一層合成樹脂製品の硬度、耐摩耗性、
耐熱性を改善し、光輝度を与えて美観を付与する
ことができることであつて、かつ金属表面処理に
より施された金属被覆膜はクラツクを生ずること
なく耐久性の良いものが得られることにある。
プラスチツクメタライジングとは合成樹脂の表
面のみに金属的性質を与える方法であつて、通常
は合成樹脂成形品の表面を脱脂し、化学エツチン
グを施して表面に多数の凹痕を形成し、次いで真
空蒸着法、無電解メツキ、陽極スパツタリング、
金属溶射法、湿式電気メツキ等の手法を単独また
は併用して施し、アルミニウム、錫、銅、ニツケ
ル、クロム等の金属被膜層を形成するものであ
り、自動車のラジエータグリル、ヘツドランプハ
ウジング、テレビまたはラジオのダイヤルのつま
み等に施され、実用化されている。
本発明においては充填材により補強された熱可
塑性合成樹脂(FRTP)の基材60の一面に層着
せしめた充填材を含まない熱可塑性合成樹脂(ナ
チユラル材)の表面に、常法により化学腐蝕液で
処理(エツチング)した後上記金高表面処理を施
すものであるから、処理により形成された金属皮
膜層はナチユラル材の表面と同様の滑らかな表面
を形成するので、FRTPい直接施した金属皮膜層
のような凹凸はなく平滑度も光輝性も極めて良好
であり、かつナチユラル材のみの製品に直接施し
た金属皮膜層と比較して密着性、耐久性に優れて
いる。これは本発明による合成樹脂製品はFRTP
の基材60とナチユラル材の表層50の層着構造
であり、ナチユラル材の表層50の熱膨脹係数が
3〜19×10-5/℃であるのに対しメタライジング
皮膜を形成する金属の熱膨脹係数が0.84〜1.65×
10-5/℃(銅、ニツケル、クロム)と大幅の差異
があつて、両者のみの接着層は熱膨脹係数の差に
より金属皮膜層にクラツクを発生するものと考え
られるが、本発明による製品においては基材60
を構成するFRTPの熱膨脹係数が1.5〜3.0×
10-5/℃であることから、ナチユラル材の表層5
0の線膨脹を低下せしめてクラツクの発生を阻止
するものと考えられる。
なお、化学腐蝕液による処理(エツチング)
は、通常ペンタン、ヘキサン、ヘブタン、オクタ
ン、ノナン、デカン、ガソリン、石油エーテル、
石油ベンジン、リグロイン、ケロシン、流動パラ
ピン、ベンゼン、トルエン、キシレン、メタノー
ル、エタノール、プロパノール、ブタノール、オ
クタノール、アルコール等の溶剤またはクロム酸
酸化液、苛性アルカル液等の薬品で合成樹脂成形
体の表面処理を施して成形体の表面に凹痕を形成
粗面化せしめ、該凹痕の中にまでメツキがつきま
わり投錨効果をあらわすためのものであり、樹脂
の種類によつてはエツチングの前に前処理(予備
エツチング)を施し、あるいは塩化第1錫の塩酸
酸性液中に成形体を浸漬して表面に2価の錫イオ
ンを吸着させるセンシタイジングおよび塩化パラ
ジウムの塩酸酸性液に成形体を浸漬して表面に金
属パラジウムを折出させるアクチベーシヨンを行
うことがある。
実施例 1
ポリカーボネート樹脂の表層51、該ポリカー
ボネート樹脂にガラス繊維(一般市販品)を30重
量%混合した繊維強化ポリカーボネート樹脂の基
体61を層着し、表層51の表面全面に金属皮膜
層70を施した自動車ドア用ハンドル(ドア内側
用)を成形する。このハンドルは第2図に斜面図
を、第3図に側面図を、第4図に上面図を、第5
図に背面図を、第6図および第7図に断面図を
夫々示すように、上面が口字状を呈し、前端に把
手辺21、後端に取付辺22を配し、該取付辺2
2の下面には3個の突片23,24,25を突設
し、これら突片23,24,25に同軸上に穿設
した孔26によりドアに枢支され、中央の突片2
4の自由端に穿設した孔27にドアロツク装置を
連係するものである。そして該ハンドルの寸法は
上面において45mm×70mmの外形寸法を有し、最上
面から2mmの深さの部分がポリカーボネート樹脂
により成形された表層51であり、残部は繊維強
化ポリカーボネート樹脂により成形された基材6
1である。
上記ハンドルを成形するため第1図に示す二重
射出成形機を用い、第1の金型8には該ハンドル
の第3図2点鎖線−より上部の形状を成形す
る型面7を形成せしめ、第2の金型9には第3図
1点鎖線−に沿う断面形状の型面を形成せし
め、第3の金型10には第3図2点鎖線−よ
り下部の形状を成形する型面12を形成せしめ
た。
このような金型8,9,10をそれぞれ可動板
4、固定板3に固着せしめ、金型を90℃に予熱
し、第1の射出ステーシヨン15において射出シ
リンダ14、孔13を介して型面7,11間にポ
リカーボネート樹脂を温度300℃、射出圧力1200
Kg/cm2で圧入充填せしめ、直ちに可動フレーム5
を後退させ、可動板4を180度回転させて再び可
動フレーム5を前進させ、第2の射出ステーシヨ
ン18において前記金型8を第3の金型10と結
合せしめ、既に金型8の型面7に装着されている
ポリカーボネート樹脂の裏面と型面12との間
に、前記繊維補強ポリカーボネート樹脂を温度
320℃、射出圧力1300Kg/cm2で圧入充填せしめ、
樹脂の硬化を待つて金型8,10から成形品ハン
ドルを取り出した。
この成形品はポリカーボネート樹脂の表層51
の表面は鏡面状の光沢に富んだ極めて平滑な表面
を呈し、ハンドルの上面即ち自動車のドア内面に
装着した場合に視野に入る表面の約70%は表層5
1の表面が占めており、繊維強化ポリカーボネー
ト樹脂の基材61は重量にしてほぼ90%以上を占
めるにも拘らず前記視野に入る表面は極めて僅か
であり、ハンドルとして十分な強度を有してい
た。しかもハンドルを縦断した断面は表層51と
基材61が層状をなし、かつその接合面は混合成
層をなして接着していた。
この成形ハンドルに常法によりプラスチツクメ
タライジング手法で金属処理を施した。即ち成形
ハンドルを脱脂後、ジメチルホルムアミド液中に
浸漬する予備エツチングを施して水洗し、次いで
クロム酸と硫酸の混液中でエツチングを施し、さ
らに塩化第一錫の塩酸酸性液中に浸漬するセンシ
タイジング、塩化パラジウムの塩酸酸性液に浸漬
するアクチベーシヨンを施した後、湿式で銅メツ
キ、ニツケルメツキおよびクロムメツキを施し金
属皮膜層70を形成した。この金属皮膜層70は
ハンドルの表層51の全表面に形成され、鏡面の
光輝性が高く美観も極めて良好なものであつた。
実施例 2
実施例1の金型8と第2の金型9を用い、金型
を120℃に予熱してポリアリレート樹脂(ユニチ
カ製商品名Uポリマー)を360℃の温度に溶融し
1400Kg/cm2の射出圧力で表層51を成形し、冷却
後これを取出して待機させた。
実施例1の金型8と第3の金型10を120℃に
予熱し、前記別途成形した表層51を第1の金型
8の所定の型面に装着し、金型8と金型10とを
結合させ、前記表層51と金型10の型面12と
の間に、ガラス繊維(一般市販品)の30重量%を
前記ポリアリレート樹脂に混合したガラス繊維補
強合成樹脂を390℃に溶融し、1600Kg/cm2の射出
圧力で圧入充填して基材61を成形すると同時
に、前記表層51と一体化層着せしめた。成形ハ
ンドルの表層51の光沢度および基材61との接
着性は実施例1の成形ハンドルと同様であつた。
この成形ハンドルに実施例1と同一手法で金属
皮膜70を施した。その外観および光輝性も実施
例1の成形ハンドルと同様であつた。
実施例 3
ポリアミド樹脂の厚さ0.4mmのフイルムシート
を真空成形機により260℃に加熱し2分間加熱し
て所望のハンドルの上面形状に真空成形し、これ
を4分間冷却してとり外し、実施例2の表層51
とほぼ同一表面積に切りとつた。
実施例1の金型8と第3の金型10とを70℃に
予熱し、金型8の型面7の所定個所に前記真空成
形した表層を装着し、金型8と金型10とを結合
した後、表層と型面12との間に、ガラス繊維
(一般市販品)の30重量%を前記ポリアミド樹脂
に混合したFRTPを300℃に溶融せしめ、850Kg/
cm2の射出圧力で圧入充填し、前記表層に基材を一
体化せしめた。
この成形ハンドルの表層の光沢度および基材と
の接着性、ならびにこの成形ハンドルに実施例1
と同一手法で金属皮膜層を施した場合の外観およ
び光輝性は、ともに実施例1の成形ハンドルと同
様であつた。
比較例 1
実施例1の金型8および第3の金型10を結合
し、90℃に予熱して、型面7,12間の型空間に
300℃に溶融せしめたポリカーボネート樹脂を
1200Kg/cm2の射出圧力で圧入充填せしめて、ナチ
ユラル材のみのハンドルを成形し、実施例1と同
一手法で金属皮膜層を形成させた。
比較例 2
実施例1の金型8および第3の金型10を結合
し、90℃に予熱して型面7,12間の型空間に、
320℃に溶融した一般市販品のガラス繊維の30重
量%をポリカーボネート樹脂に混合したFRTPを
1300Kg/cm2の圧力で圧入充填してFRTPのみのハ
ンドルを成形し、実施例1と同一手法で金属皮膜
層を形成させた。
叙上の各実施例および比較例で得た各成形品の
試験結果を次表に示し諸特性を比較検討する。
The present invention relates to a method for producing a thermoplastic synthetic resin product reinforced with fillers such as glass fibers and inorganic powders, which provides high optical selectivity to the surface layer. Synthetic resin products mixed with fillers such as glass fibers and inorganic powders have properties such as high strength, heat resistance, and abrasion resistance due to the inclusion of fillers. Widely used in combination with synthetic resin materials. Particularly in the automobile industry, home appliance industry, etc., they are widely put into practical use because of their light weight and good workability, and are generally referred to as engineering plastics. However, engineering plastics include polymethyl methacrylate, epoxy, polyphenylene oxide, polycarbonate, ABS, nylon, polyarylate, polypropylene, polyoxymethylene, polybutylene terephthalate, polystyrene, unsaturated polyester, diacetate, triacetate, There are molded parts made of many individual or copolymer resins such as urea, melamine, and phenol. This has been compensated for by painting or metal plating, but this has the drawback of requiring an extremely large number of man-hours to obtain a product with good surface gloss. In addition, when a metal coating film such as plating is formed directly on the surface of a resin product containing a filler, the fibers or powder of the filler protrude from the surface during treatment with a chemical etching solution, causing unevenness on the plating surface. , the gloss becomes poor and the appearance loses its beauty. In order to repair these irregularities, it is possible to apply a thick plating film, but this would be unnecessarily labor-intensive and would not be suitable for industrial production. In view of the above facts, the present invention aims to improve the strength, rigidity, abrasion resistance, etc. of the product by forming a molded body from a thermoplastic synthetic resin mixed with fillers such as glass fiber and inorganic powder as the base of the synthetic resin product. In addition to improving various properties, a surface layer of a thermoplastic synthetic resin containing no filler is applied to part or all of the surface of the product, forming a surface with good gloss on the surface layer, and further improving the surface layer. This is a synthetic resin product that has been treated with a metal surface to form a highly luminous metal film layer, and the metal film layer may develop external defects such as blistering, peeling, and cracking even after long-term use. This is a method for manufacturing synthetic resin products that aims to provide products in extremely small quantities.The feature is that either the base material or the surface layer of the product is first molded, and then the mold surface of the mold is molded. a first step of mounting the other of the base material or the surface layer on the mold, and then melting the other of the base material or the surface layer, filling and molding the mold space of the mold, and first mounting the molded body on the mold surface of the mold. While softening or melting the surface of the molded product, a mixed layer is formed in the contact area with the molded product that is later filled and molded,
a second step of forming a mixed layer on the base material and the surface layer at the contact area thereof to form an integral bonding layer;
A third step of taking out the layered molded body of the base material and the surface layer from the mold, treating the surface of the surface layer with a chemical etching solution by a conventional method, and then applying a metal surface treatment to form a metal film layer. This relates to a method for manufacturing synthetic resin products consisting of: Furthermore, preferably in the present invention, the molded body of either the base material or the surface layer is formed using a second mold that utilizes a predetermined mold surface within the mold space of the mold and forms the molded body. The other of the base material or the surface layer is melted or filled with the first metal while the other molded body is in a melted or uncured state. Melting the synthetic resin to form the other molded body in the mold space of the product shape formed by the mold and the third mold,
The material is filled, and a mixed layer is formed at the contact area between the base material and the surface layer to integrate the base material and the surface layer. The resin used in the present invention can be any of the thermoplastic synthetic resins used in the engineering plastics mentioned above, but a preferable resin with good compatibility for integrating the two layers of the base material and the surface layer by mixed layering is polyolefin. , polyarylate,
It is a single or copolymer of polymethacrylate, polystyrene, polyvinyl halide, polyamide, polyester, polycarbonate, polyacrylonitrile, etc. As fillers, inorganic fibers such as glass fibers, asbestos, and carbon fibers, organic fibers such as vinylon fibers, and inorganic powders such as metal powders, carbon powders, and graphite powders can be used, but inorganic fibers are generally used. preferable. If the length of the filler fiber is long, the flow of the molten synthetic resin will be poor, and it will be difficult to mold it in a mold with a dense mold surface. Otherwise, it has little effect in reinforcing the product and can also make the product brittle. Although there are differences depending on the nature of the parts used in functional parts such as automobile parts, in decorative parts the fiber length is 0.4 to 4 mm, the wire diameter is 1.0 to 10 -4 mm,
Single fibers with a cross-sectional area of 0.8 to 8 x 10 -7 mm 2 are preferred. The filler is kneaded with a synthetic resin in advance to form a compound or chip shape, which is then molded using an injection molding machine. The present invention will be explained based on an implementation method in which a first mold is combined with a second and third mold to perform double injection molding. FIG. 1 shows an outline of an injection molding machine used in the above method, in which a fixing plate 3 is fixed to a base 1 by an appropriate method by means of supporting rods 2, 2. and a movable plate 4 are disposed to face each other, and the movable plate 4 is reciprocated by the bearing rods 2, 2 toward the fixed plate 3 or away from the fixed plate 3. The frame 5 is rotatably supported by a support shaft 6. The movable plate 4 has two first molds 8, 8 having mold surfaces 7, 7 engraved thereon to form one side of a desired resin product.
are fixed at rotation angle positions of 180 degrees at equal distances from the center of the support shaft 6, and on the other hand, a second mold 9 and a third mold 10 are mounted on the fixed plate 3 at the same distance with respect to the center of rotation of the movable plate 4. The movable plate 4 is fixed at a rotation angle position of 180 degrees in terms of distance and at a position where it is simultaneously connected to the first molds 8, 8, respectively, when the movable plate 4 is slid forward by the support rods 2, 2. . The second mold 9 has a mold surface 11 that is to mold the surface layer of a desired product together with the mold surface 7 of the first mold 8 when the mold 9 is combined with the first mold 8. The third mold 10 has a first mold 8 when the mold 10 is combined with the first mold 8.
Along with the mold surface 7 of the mold 8, a mold surface 12 is engraved to form the shape of a desired product. The fixing plate 3 has a hole 1 opened to the mold surface 11 of the second mold 9.
3, the injection cylinder 14 is fixed to open,
First injection molding station 15 with mold 9
Further, a second injection station 1 is fixed such that an injection cylinder 17 opens in a hole 16 opening in the mold surface 12 of the third mold 10.
8. The embodiment of the present invention using the injection molding machine shown in FIG. 1 is as follows. The molds 8, 9, and 10 are sufficiently heated, the movable plate 4 is moved forward by the movable frame 5, and the second mold 9 and the third mold 10 are placed in the first molds 8 and 8, respectively. to combine. First, in the first injection station 15, a thermoplastic synthetic resin (natural material) without a filler mixed therein is press-fitted in a molten state from the injection cylinder 14 through the hole 13, and is filled into the mold space between the mold surfaces 7 and 11. A surface layer 50 of the desired product is molded. Next, the movable plate 4 is moved while the surface of the synthetic resin forming the surface layer 50 is slightly cooled and maintains its shape but is still molten inside or the surface layer 50 is unhardened and soft. When the first mold 8 with the surface layer 50 attached to the mold surface 7 is moved backward, rotated 180 degrees around the rotation center, and moved forward again, the first mold 8 with the surface layer 50 attached to the mold surface 7 is combined with the third mold 10 at the second injection station 18. be done. Mold surface 12 of third mold 10
The second injection station 18 forms a mold space with the shape of the desired product together with the mold surface 7 of the mold 8.
When a thermoplastic synthetic resin (FRTP) mixed with a filler is melted and press-fitted into the mold space through the injection cylinder 17 and the hole 16 to fill the mold space, the FRTP forms the surface layer 50 of the natural material and the third layer.
Since the surface layer 50 of the natural material is still at a high temperature, it becomes molten at the contact surface with the FRTP base material 60 that is press-fitted. Since the two are integrated, when the product is taken out after cooling in the molds 8 and 10,
The natural material surface layer 50 and the FRTP base material 60 are integrated at their contact surfaces by mixed layering to obtain a layered product. Since the surface layer 50 of this product is a natural material that does not contain fillers, it has a glossy surface that matches the surface finish of the mold surface 7, and the base material 6
0 is FRTP mixed with fillers, so it has high strength, toughness, heat resistance, and durability, and the surface layer 5
0 and the base material 60 are integrated by mixed layering,
Its adhesive strength is extremely strong. In the present invention, the surface layer 50 is formed to give gloss to the surface of the product and give it a beautiful appearance, so a thickness of about 0.2 to 1.5 mm is appropriate even for functional products such as automobile parts. In carrying out the present invention, the mold surface 7 of the first mold 8 is used as the mold surface on which the base material 60 by FRTP is to be molded, and the base material 60 is first molded at the first injection station 15, and then the second mold is molded. It is also possible to use the mold surface 12 of the injection station 18 as the mold surface on which the surface of the surface layer 50 is to be molded, and to injection mold the surface layer 50 at the second injection station 18 so as to integrate it with the base material 60. In the method using this double injection molding machine, the surface layer 5 is
0 or the base material 60 by injection molding, the movable plate 4 is retreated, rotated 180 degrees, and moved forward again, and the other injection molding is performed at the second injection station 18. Therefore, the moving time between molding at the first injection station 15 and molding at the second injection station 18 can be made extremely short.
The surface layer 5 molded by the injection station 15 of
The molded body of either 0 or the base material is subjected to injection molding at the second injection station 18 in a state in which only the surface thereof is molded and the inside is molten or in an uncured soft state to form the desired product. Therefore, it is extremely easy to mix and stratify the contact surface between the surface layer 50 and the base material 60, and the melting temperature of the synthetic resin in the second injection molding station 18 can be adjusted to the melting temperature of the synthetic resin in the first injection molding station 15. About 10-40℃ above melting temperature, preferably 20-35℃
If the temperature is high, the surface layer 5 will be removed in a normal injection molding cycle.
A product with good adhesion between the base material 60 and the base material 60 can be obtained. Further, as understood from the above-mentioned implementation method of the present invention, in the present invention, the surface layer 50 or the base material 6
It is also possible to adopt an implementation method in which either one of the two parts is molded in advance, the molded product is mounted in the mold space of an injection molding machine, and the synthetic resin to be formed with the other part is melted and injection molded. That is, if this is explained using the symbols in FIG.
Using the first mold 8 and the second mold 9, a natural material is injection molded to form a large number of surface layers 50 in advance. Next, using the first mold 8 and the third mold 10, the preformed surface layer 50 is attached to the mold surface 7 of the first mold 8, which has been preheated to a sufficiently high temperature, and the third mold The mold 10 is joined to the first mold 8, and FRTP is formed between the surface layer 50 and the mold surface 12 of the third mold 10.
When injection molding is performed by melting the FRTP to a sufficiently high temperature, the surface of the surface layer 50 attached to the mold 8 that is in contact with the molten FRTP is melted or softened at that temperature, forming a mixed layer of FRTP and natural materials. It is integrated with the base material 60 and can be layered. In this implementation method, the base material 60 is
Of course, the surface layer 50 may be formed by molding with FRTP and then molding a natural material onto one surface of the base material 60 by injection molding using an injection molding machine.
Alternatively, one of the base materials 60 preferably has a composition structure that is melted or softened at the injection temperature of the other synthetic resin to be molded later, and it is preferable that the filling pressure of the resin performed later is sufficiently high. . Another feature of the present invention is that, as described above, the surface layer 50 of a natural material with good gloss is coated on a part or all of the surface of the FRTP base material 60 with good adhesion. By applying metal surface treatment using plastic metallization on the surface of the product, the hardness, abrasion resistance, and
It is possible to improve heat resistance, give brightness and give a beautiful appearance, and the metal coating film applied by metal surface treatment can be obtained with good durability without causing cracks. be. Plastic metallizing is a method of imparting metallic properties only to the surface of synthetic resin. Usually, the surface of a synthetic resin molded product is degreased, chemically etched to form a large number of grooves on the surface, and then vacuum etched. Vapor deposition method, electroless plating, anodic sputtering,
Metal spraying, wet electroplating, and other methods are applied alone or in combination to form a metal coating layer of aluminum, tin, copper, nickel, chrome, etc., and can be applied to automobile radiator grills, headlamp housings, televisions, etc. It has been put into practical use on radio dial knobs, etc. In the present invention, the surface of a thermoplastic synthetic resin (natural material) that does not contain a filler and is layered on one side of the base material 60 of a thermoplastic synthetic resin (FRTP) reinforced with a filler is chemically etched by a conventional method. Since the metal surface treatment described above is applied after treatment (etching) with a liquid, the metal film layer formed by the treatment forms a smooth surface similar to the surface of natural materials, so FRTP is a metal that is directly applied. It has no irregularities like a film layer, and has extremely good smoothness and brightness, and has superior adhesion and durability compared to a metal film layer applied directly to a product made only of natural materials. This is the synthetic resin product according to the present invention that is FRTP.
It has a layered structure of a base material 60 and a natural material surface layer 50, and the thermal expansion coefficient of the natural material surface layer 50 is 3 to 19×10 -5 /°C, whereas the thermal expansion coefficient of the metal forming the metallizing film is is 0.84~1.65×
10 -5 /℃ (copper, nickel, chromium), and it is thought that cracks occur in the metal film layer due to the difference in coefficient of thermal expansion in the adhesive layer of only the two, but in the product according to the present invention. is base material 60
The thermal expansion coefficient of FRTP is 1.5~3.0×
10 -5 /℃, the surface layer of natural wood 5
It is thought that this reduces the zero linear expansion and prevents the occurrence of cracks. In addition, treatment with chemical corrosive solution (etching)
Usually contains pentane, hexane, hebutane, octane, nonane, decane, gasoline, petroleum ether,
Surface treatment of synthetic resin moldings with solvents such as petroleum benzine, ligroin, kerosene, liquid parapine, benzene, toluene, xylene, methanol, ethanol, propanol, butanol, octanol, alcohol, etc., or chemicals such as chromic acid oxidizing liquid, caustic alkal liquid, etc. The purpose is to form concave marks on the surface of the molded product and roughen it, and the plating extends into the concave marks to create an anchoring effect. Depending on the type of resin, it is Treatment (pre-etching) or sensitizing, in which divalent tin ions are adsorbed to the surface by immersing the molded body in an acidic solution of stannous chloride in hydrochloric acid, and immersion of the molded body in an acidic solution of palladium chloride in hydrochloric acid. Activation is sometimes performed to precipitate metal palladium on the surface. Example 1 A surface layer 51 of polycarbonate resin, a base body 61 of fiber-reinforced polycarbonate resin in which 30% by weight of glass fiber (commercially available product) is mixed with the polycarbonate resin are layered, and a metal film layer 70 is applied to the entire surface of the surface layer 51. molded car door handles (for the inside of the door). This handle is shown in a slope view in Figure 2, a side view in Figure 3, a top view in Figure 4, and a top view in Figure 5.
As shown in the rear view in Fig. 6 and in cross-section in Figs.
Three protruding pieces 23, 24, 25 are provided protrudingly on the lower surface of 2, and are pivoted to the door through holes 26 coaxially drilled in these protruding pieces 23, 24, 25.
A door lock device is linked to a hole 27 drilled in the free end of the door lock 4. The handle has external dimensions of 45 mm x 70 mm on the top surface, and a portion 2 mm deep from the top surface is a surface layer 51 molded from polycarbonate resin, and the rest is a base layer 51 molded from fiber-reinforced polycarbonate resin. Material 6
It is 1. In order to mold the handle, a double injection molding machine shown in FIG. 1 is used, and the first mold 8 is formed with a mold surface 7 for molding the shape of the handle above the two-dot chain line in FIG. , the second mold 9 is formed with a mold surface having a cross-sectional shape along the dashed dotted line in FIG. A surface 12 was formed. These molds 8, 9, and 10 are fixed to the movable plate 4 and the fixed plate 3, respectively, and the molds are preheated to 90°C. Between 7 and 11, polycarbonate resin was heated at a temperature of 300℃ and an injection pressure of 1200℃.
Kg/cm 2 was press-fitted, and the movable frame 5 was immediately filled.
is moved backward, the movable plate 4 is rotated 180 degrees, and the movable frame 5 is advanced again, and the mold 8 is combined with the third mold 10 at the second injection station 18, and the mold surface of the mold 8 is already The fiber-reinforced polycarbonate resin is heated between the back surface of the polycarbonate resin attached to the mold surface 12 and the mold surface 12.
Press-fitted at 320℃ and injection pressure of 1300Kg/ cm2 .
After waiting for the resin to harden, the molded product handles were taken out from the molds 8 and 10. This molded product has a surface layer 51 of polycarbonate resin.
has an extremely smooth surface with a mirror-like luster, and approximately 70% of the surface visible when mounted on the top of the steering wheel, i.e. the inside surface of a car door, is the surface layer 5.
Although the base material 61 made of fiber-reinforced polycarbonate resin accounts for more than 90% of the weight, the surface that falls within the field of view is extremely small and does not have sufficient strength as a handle. Ta. Moreover, in a cross section taken through the handle, the surface layer 51 and the base material 61 formed a layered structure, and their joint surfaces were bonded together in a mixed layered manner. This molded handle was metallized using a plastic metallizing method in a conventional manner. That is, after the molded handle is degreased, it is pre-etched by immersing it in a dimethylformamide solution, washed with water, then etched in a mixture of chromic acid and sulfuric acid, and then immersed in an acidic solution of stannous chloride in hydrochloric acid. After activation by immersion in an acidic solution of palladium chloride in hydrochloric acid, copper plating, nickel plating and chrome plating were performed in a wet manner to form a metal film layer 70. This metal film layer 70 was formed on the entire surface of the surface layer 51 of the handle, and had a high mirror shine and an extremely good appearance. Example 2 Using the mold 8 of Example 1 and the second mold 9, the molds were preheated to 120°C and polyarylate resin (product name U polymer manufactured by Unitika) was melted to a temperature of 360°C.
The surface layer 51 was molded at an injection pressure of 1400 Kg/cm 2 , and after cooling, it was taken out and kept on standby. The mold 8 and the third mold 10 of Example 1 are preheated to 120° C., the separately molded surface layer 51 is attached to a predetermined mold surface of the first mold 8, and the mold 8 and the third mold 10 are heated. A glass fiber-reinforced synthetic resin prepared by mixing 30% by weight of glass fiber (commercially available product) with the polyarylate resin is melted at 390°C between the surface layer 51 and the mold surface 12 of the mold 10. Then, the base material 61 was formed by press-filling at an injection pressure of 1600 Kg/cm 2 , and at the same time, an integrated layer was formed with the surface layer 51 . The glossiness of the surface layer 51 of the molded handle and the adhesion to the base material 61 were similar to those of the molded handle of Example 1. A metal coating 70 was applied to this molded handle using the same method as in Example 1. Its appearance and shine were also similar to the molded handle of Example 1. Example 3 A film sheet of polyamide resin with a thickness of 0.4 mm was heated to 260°C using a vacuum forming machine, heated for 2 minutes, vacuum formed into the desired shape of the upper surface of the handle, cooled for 4 minutes, removed, and carried out. Surface layer 51 of example 2
It was cut to approximately the same surface area. The mold 8 of Example 1 and the third mold 10 are preheated to 70° C., the vacuum-formed surface layer is attached to a predetermined portion of the mold surface 7 of the mold 8, and the mold 8 and the third mold 10 are After bonding, between the surface layer and the mold surface 12, FRTP containing 30% by weight of glass fiber (commercially available product) mixed with the polyamide resin was melted at 300℃, and 850Kg/
The material was press-fitted with an injection pressure of cm 2 to integrate the base material with the surface layer. The glossiness of the surface layer of this molded handle and the adhesion to the base material, and
When a metal film layer was applied using the same method as in Example 1, both the appearance and brightness were similar to those of the molded handle of Example 1. Comparative Example 1 The mold 8 of Example 1 and the third mold 10 were combined, preheated to 90°C, and the mold space between the mold surfaces 7 and 12 was heated.
Polycarbonate resin melted at 300℃
A handle made only of natural materials was formed by injecting and filling at an injection pressure of 1200 Kg/cm 2 , and a metal film layer was formed using the same method as in Example 1. Comparative Example 2 The mold 8 of Example 1 and the third mold 10 were combined, preheated to 90°C, and the mold space between the mold surfaces 7 and 12 was filled with
FRTP is made by mixing 30% by weight of commercially available glass fiber melted at 320℃ with polycarbonate resin.
A handle made only of FRTP was formed by press-filling at a pressure of 1300 Kg/cm 2 , and a metal film layer was formed using the same method as in Example 1. The test results of each molded article obtained in each of the above-mentioned Examples and Comparative Examples are shown in the following table, and various characteristics are compared and examined.
【表】【table】
【表】
上記表において、ヒート・サイクル・テストと
は、80℃×60分→21℃×10分→−30℃×60分→21
℃×10分を1サイクルとしてこのサイクルを4回
繰り返し、フクレ、ハガレ、割れ等外観上の欠陥
の発生を観察する試験であり、ヒートサイクル
CASSテストとは上記ヒートサイクルテストを1
サイクル終了したものをCASS(米国標準規格
ASTM、B−368)にかけ、これを3回繰り返し
てフクレ、剥離、割れ、腐蝕生成物発生状況など
を観察する試験であり、サーマルシヨツクテスト
とは、−40℃×60分→130℃×60分を1サイクルと
してこのサイクルを4回繰り返し、フクレ、剥
離、割れ等の外観上の欠陥の発生を観察する試験
である。またピーリングテストとは、メツキ幅10
mm、ピーリング速さ30mm/分で、オートグラフを
使用し合成樹脂面における密着性を測定する試験
であり、コロードコートとは日本標準規格JIS、
D−0201付属書1によるもので、硝酸塩0.035
g、塩化第2鉄0.165g、塩化アンモニウム1.0
g、水50c.c.、白陶土30gのペーストを合成樹脂上
に25〜100μの厚さに塗布し、室温で1時間放置
して乾燥させ、これを38±2℃、相対湿度80〜99
%の湿気室中に16時間放置した後、流水でペース
トを流し去り、腐蝕状況を見る試験である。さら
に耐熱テストは80℃、100℃、120℃、140℃の各
雰囲気中において4時間放置し、フクレ、剥離、
割れ等の外観上の欠陥を観察する試験である。な
お曲げ強度は日本標準規格JIS、K−7203の「硬
質プラスチツクスの曲げ試験方法」に基き、常法
により装飾クロームメツキ処理した曲げテストピ
ースによつて測定したものである。
上記表によつて明らかなように、本発明方法に
よつて成形された製品は表面の光輝性において比
較例1のナチユラル材のみの成形品と同等である
が、比較例2に示すFRTPのみの成形品は光輝度
において著るしく劣り、しかも各種試験によりナ
チユラル材のみの比較例1の成形品はメツキ面に
割れを生じたが、本発明方法によつて成形された
製品はメツキ面に何の損傷も認められず、強度
(耐熱テストを含む)においては、本発明方法に
より成形された製品はナチユラル材のみの比較例
1に示す成形品よりは著るしく大であり、かつ
FRTPのみの実施例2に示す成形品と同等または
それ以上であることがわかる。
以上のように、本発明は、熱可塑性合成樹脂の
製品を成形するにあたり、該樹脂のみ(ナチユラ
ル材)による成形品と同等の光沢度、光輝度を有
する外観を保たせ、かつ該樹脂にガラス繊維、無
機質粉末等の充填材を混合した補強熱可塑性合成
樹脂のみ(FRTP)の成形品と同等またはそれ以
上の強度を保有する製品を得ることを目的とし、
前記ナチユラル材による成形体の表層と前記
FRTPによる成形体の基材とを混合成層により一
体に層着させ、さらに表層の表面の一部または全
部に金属皮膜層を形成せしめる方法であつて、前
記製品を成形すべき型面を形成した型空間を有す
る金型に前記基材または表層の何れか一方の成形
体を前記型面に適合せしめて装着する第1工程
と、前記金型に装着した成形体の少くとも型空間
内に露呈する面が軟化ないし溶融する温度範囲に
おいて、前記基材または表層の他方を成形すべき
合成樹脂を溶融せしめて前記金型の型空間の残部
に充填、成形せしめることにより、前記基材およ
び表層を一体に接合せしめる第2工程とを結合し
たことにより、前記表層と基材とは金型の型面に
より所望製品の所望の位置に形成され、かつ両者
の接合面は表層および基材の成形材料の混合成層
で一体に接着されるから接着力は強力であり、充
填材により補強された基材の強度とナチユラル材
の表層の光沢度と平滑光輝度とを併せ有する合成
樹脂製品を得ることができる。
また本発明によるときは、前記第1工程におい
て前記基材または表層の何れか一方の成形体の表
面を成形する型面を有する金型とその裏面を成形
する第2の金型とを結合して該成形体を成形し、
次いで第2工程において第2の金型に代え製品の
残部の表面を成形する型面を有する第3の金型を
前記第1の金型に結合して、前記基材または表層
の他方の成形体の充填成形を行うときは、二重射
出成形機等を利用して短時間に製品の成形ができ
るとともに、第1の金型内で先に成形した成形体
が表面のみ成形されて内部が溶融状態にあるか、
あるいは全体が未硬化の軟かい状態において後に
成形する成形体の成形が行われるので、その接合
面の混合成層が極めて容易に形成できる特長を有
するものである。
さらに本発明によるときは、第3工程におい
て、上記のように成形層着された成形品のナチユ
ラル材の表層の表面に、常法により化学腐蝕液で
処理した後金属表面処理を施すから、製品表面に
平滑性のよい金属皮膜層を形成でき、かつ該金属
皮膜層は熱膨脹係においてかなりの差異があるナ
チユラル材の表層面に形成されるが、該表層は熱
膨脹係数において両者の中間値をとるFRTPの基
材に線膨脹を抑制されるため、クラツクやフク
レ、剥離の発生し難い金属皮膜層を形成できる特
長を有するものである。
従つて本発明は、自動車部品、家庭電化製品そ
の他の装飾部品の製造に止まらず、機能部品の製
造に応用して、外観を良好にするのみでなく、平
滑性と強度を良好にし、さらには表層表面に金属
皮膜層を形成して耐熱性耐蝕性を増強するととも
に、電気的性質を要求される機能部品の耐久性を
増強するものである。[Table] In the above table, heat cycle test is 80℃ x 60 minutes → 21℃ x 10 minutes → -30℃ x 60 minutes → 21
This test is a test in which the cycle is repeated 4 times with 10 minutes at ℃ x 10 minutes to observe the occurrence of external defects such as blisters, peeling, and cracks.
CASS test is the heat cycle test mentioned above.
CASS (American standard)
ASTM, B-368) is repeated three times to observe blistering, peeling, cracking, and the occurrence of corrosion products. This is a test in which this cycle is repeated four times, with minutes being one cycle, and the occurrence of external defects such as blistering, peeling, and cracking is observed. Also, the peeling test means that the peeling width is 10
This is a test that measures adhesion to a synthetic resin surface using an autograph at a peeling speed of 30 mm/min.
According to D-0201 Annex 1, nitrate 0.035
g, ferric chloride 0.165 g, ammonium chloride 1.0
A paste of 50 g, 50 c.c. of water, and 30 g of white china clay was applied onto a synthetic resin to a thickness of 25 to 100 μm, left to dry at room temperature for 1 hour, and then heated to 38 ± 2° C. and relative humidity of 80 to 99
This test involves leaving the paste in a humidity chamber for 16 hours, then washing it off with running water to check for corrosion. Furthermore, the heat resistance test was performed by leaving the product in an atmosphere of 80℃, 100℃, 120℃, and 140℃ for 4 hours to prevent blistering, peeling,
This is a test to observe external defects such as cracks. The bending strength was measured based on the Japanese standard JIS K-7203 "Bending test method for hard plastics" using a bending test piece treated with decorative chrome plating in a conventional manner. As is clear from the above table, the product molded by the method of the present invention has the same surface brightness as the molded product made only of natural materials in Comparative Example 1, but the product molded by the method of the present invention is equivalent to the molded product made only of natural materials shown in Comparative Example 2. The molded product was significantly inferior in brightness, and various tests showed that the molded product of Comparative Example 1, which was made only of natural materials, had cracks on the plating surface, but the product molded by the method of the present invention had no cracks on the plating surface. No damage was observed, and in terms of strength (including heat resistance tests), the product molded by the method of the present invention was significantly greater than the molded product shown in Comparative Example 1 made of natural materials only, and
It can be seen that the molded product shown in Example 2 containing only FRTP is equivalent to or better than that of the molded product shown in Example 2. As described above, when molding a product made of thermoplastic synthetic resin, the present invention maintains an appearance with the same level of gloss and brightness as a molded product made only of the resin (natural material), and also allows the resin to be made of glass. The aim is to obtain a product that has strength equal to or greater than that of a molded product made only of reinforced thermoplastic synthetic resin (FRTP) mixed with fillers such as fibers and inorganic powder.
The surface layer of the molded article made of the natural material and the
A method in which the base material of the FRTP molded product is integrally layered by mixed layering, and a metal film layer is further formed on part or all of the surface layer, and the mold surface on which the product is to be molded is formed. A first step of fitting either the base material or the surface layer into a mold having a mold space and fitting the molded object to the mold surface, and exposing at least the molded object installed in the mold into the mold space. The base material and the surface layer are molded by melting the synthetic resin that is to be molded into the other of the base material or the surface layer, and filling and molding the synthetic resin into the remaining mold space of the mold in a temperature range in which the surface to be molded softens or melts. By combining the second step of joining them together, the surface layer and the base material are formed at the desired position of the desired product by the mold surface of the mold, and the joint surface of both is formed by the molding material of the surface layer and the base material. Because they are bonded together in a mixed layer, the adhesive force is strong, and it is possible to obtain a synthetic resin product that has both the strength of the base material reinforced by the filler and the gloss and smooth brightness of the surface layer of the natural material. can. Further, according to the present invention, in the first step, a mold having a mold surface for molding the surface of either the base material or the surface layer and a second mold for molding the back surface thereof are combined. to mold the molded body,
Next, in a second step, instead of the second mold, a third mold having a mold surface for molding the remaining surface of the product is connected to the first mold, and the other of the base material or surface layer is molded. When performing filling molding of a body, the product can be molded in a short time by using a double injection molding machine, etc., and the molded body previously molded in the first mold is molded only on the surface and the inside is molded. Is it in a molten state?
Alternatively, since the molded product to be molded later is formed in a soft, uncured state as a whole, it has the advantage that a mixed layering on the joint surfaces can be formed extremely easily. Furthermore, according to the present invention, in the third step, the surface layer of the natural material of the molded product coated with the molding layer as described above is treated with a chemical etching solution in a conventional manner, and then metal surface treatment is applied to the product. A metal film layer with good smoothness can be formed on the surface, and the metal film layer is formed on the surface layer of natural materials, which have a considerable difference in coefficient of thermal expansion, but the surface layer has a value intermediate between the two in terms of coefficient of thermal expansion. Since linear expansion is suppressed in the FRTP base material, it has the advantage of being able to form a metal film layer that is less prone to cracking, blistering, and peeling. Therefore, the present invention is applicable not only to the production of automobile parts, home appliances, and other decorative parts, but also to the production of functional parts, which not only improves the appearance but also improves smoothness and strength. A metal film layer is formed on the surface layer to enhance heat resistance and corrosion resistance, as well as the durability of functional parts that require electrical properties.
第1図は本発明を実施するに適する二重射出成
形機の要部を示す一部欠截側面図、第2図ないし
第7図は本発明によつて製造した成形品の一例を
示すもので、第2図はその斜面図、第3図はその
側面図、第4図はその正面図、第5図はその背面
図、第6図および第7図は断面図をそれぞれ示す
ものである。
なお図中1は射出成形機の基台、2は支承杆、
3は固定板、4は可動板、5は可動フレーム、6
は支軸、8,9,10は金型、7,11,12は
型面、14,17は射出シリンダ、15,18は
射出ステーシヨン、50,51は表層、60,6
1は基材、70は金属皮膜層、をそれぞれ示すも
のである。
Fig. 1 is a partially cutaway side view showing the main parts of a double injection molding machine suitable for carrying out the present invention, and Figs. 2 to 7 show examples of molded products manufactured according to the present invention. Fig. 2 is a slope view, Fig. 3 is a side view, Fig. 4 is a front view, Fig. 5 is a rear view, and Figs. 6 and 7 are cross-sectional views. . In the figure, 1 is the base of the injection molding machine, 2 is the support rod,
3 is a fixed plate, 4 is a movable plate, 5 is a movable frame, 6
8, 9, 10 are the support shafts, 8, 9, 10 are the molds, 7, 11, 12 are the mold surfaces, 14, 17 are the injection cylinders, 15, 18 are the injection stations, 50, 51 are the surface layers, 60, 6
1 indicates a base material, and 70 indicates a metal film layer, respectively.
Claims (1)
強された熱可塑性合成樹脂成形体の基材の一面の
一部または全部に前記充填材を含有しない熱可塑
性合成樹脂により成形された表層を層着して表層
が平滑な合成樹脂製品を製造する方法において、 前記製品を成形すべき型面を形成した型空間を
有する金型の前記基材または表層の何れか一方の
成形体を前記型面に適合せしめて装着する第1工
程と、 前記金型に装着した成形体の少なくとも型空間
内に露呈する面が溶融ないし軟化する温度範囲に
て前記基材または表層の他方を成形すべき合成樹
脂を溶融せしめ、前記金型の型空間の残部に充填
成形せしめ、前記基材および表層を両者の接触部
に混合成層を形成せしめて一体に接合層着せしめ
る第2工程と、 前記基材および表層の層着成形体を前記金型よ
りとり出し、前記表層の表面を常法により化学腐
蝕液で処理した後金属表面処理を施して金属皮膜
層を形成する第3工程とより成ることを特徴とす
る合成樹脂製品の製造方法。 2 前記第1工程は、前記製品の一面を成形すべ
き型面を有する第1の金型に前記基材または表層
の何れか一方の成形体の裏面を形成すべき型面を
有する第2の金型を結合せしめ、該成形体を成形
すべき合成樹脂を溶融、充填して成形することに
より行われ、 前記第2工程は、前記第1工程における第2の
金型をとり外し、前記製品の他面を成形すべき型
面を有する第3の金型を前記第1の金型に係合せ
しめ、前記基材または表層の他方を成形すべき合
成樹脂を溶融、充填せしめて成形することにより
行われることを特徴とする特許請求の範囲第1項
に記載の合成樹脂製品の製造方法。[Scope of Claims] 1. A thermoplastic synthetic resin molded article reinforced with a filler such as glass fiber or inorganic powder, in which part or all of one side of the base material is molded with a thermoplastic synthetic resin that does not contain the filler. In a method for manufacturing a synthetic resin product with a smooth surface layer by layering a surface layer, the molded body of either the base material or the surface layer of a mold has a mold space that forms a mold surface on which the product is to be molded. a first step of adapting and mounting the molded body to the mold surface, and molding the other of the base material or the surface layer in a temperature range in which at least the surface exposed in the mold space of the molded article mounted in the mold melts or softens. a second step of melting the synthetic resin to be molded and filling it into the remainder of the mold space of the mold, forming a mixed layer on the base material and the surface layer at the contact area thereof, and integrally applying the bonding layer; A third step consists of taking out the layered molded body of the base material and the surface layer from the mold, treating the surface of the surface layer with a chemical etching solution by a conventional method, and then applying a metal surface treatment to form a metal film layer. A method for manufacturing a synthetic resin product characterized by: 2. In the first step, a first mold having a mold surface for molding one side of the product is used, and a second mold surface having a mold surface for forming the back surface of either the base material or the surface layer of the molded product. This is carried out by joining molds and melting and filling the molded body with a synthetic resin to be molded, and the second step is performed by removing the second mold in the first step and molding the product. A third mold having a mold surface on which the other surface is to be molded is engaged with the first mold, and the other of the base material or the surface layer is melted and filled with a synthetic resin to be molded. A method for manufacturing a synthetic resin product according to claim 1, characterized in that the method is carried out by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7124580A JPS56166021A (en) | 1980-05-28 | 1980-05-28 | Manufacture of product in synthetic resin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7124580A JPS56166021A (en) | 1980-05-28 | 1980-05-28 | Manufacture of product in synthetic resin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56166021A JPS56166021A (en) | 1981-12-19 |
| JPS6159212B2 true JPS6159212B2 (en) | 1986-12-15 |
Family
ID=13455111
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7124580A Granted JPS56166021A (en) | 1980-05-28 | 1980-05-28 | Manufacture of product in synthetic resin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS56166021A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0626825B2 (en) * | 1990-05-22 | 1994-04-13 | 岐阜車体工業株式会社 | High-strength synthetic resin tool box manufacturing method |
-
1980
- 1980-05-28 JP JP7124580A patent/JPS56166021A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56166021A (en) | 1981-12-19 |
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