JPH08118433A - Manufacture of reinforced resin cd-rom mechanism member excellent in sliding characteristic - Google Patents
Manufacture of reinforced resin cd-rom mechanism member excellent in sliding characteristicInfo
- Publication number
- JPH08118433A JPH08118433A JP25696794A JP25696794A JPH08118433A JP H08118433 A JPH08118433 A JP H08118433A JP 25696794 A JP25696794 A JP 25696794A JP 25696794 A JP25696794 A JP 25696794A JP H08118433 A JPH08118433 A JP H08118433A
- Authority
- JP
- Japan
- Prior art keywords
- mold
- resin
- heat
- rom
- insulating layer
- 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
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 229920005989 resin Polymers 0.000 title abstract description 49
- 239000011347 resin Substances 0.000 title abstract description 49
- 229920000642 polymer Polymers 0.000 claims abstract description 31
- 239000011256 inorganic filler Substances 0.000 claims abstract description 24
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 24
- 229910052751 metal Inorganic materials 0.000 claims abstract description 10
- 239000002184 metal Substances 0.000 claims abstract description 10
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 5
- 239000012763 reinforcing filler Substances 0.000 claims description 20
- 238000001746 injection moulding Methods 0.000 abstract description 8
- 239000000945 filler Substances 0.000 abstract description 5
- 230000002349 favourable effect Effects 0.000 abstract 1
- 239000004642 Polyimide Substances 0.000 description 29
- 229920001721 polyimide Polymers 0.000 description 29
- 239000010410 layer Substances 0.000 description 23
- 238000000465 moulding Methods 0.000 description 14
- 239000002243 precursor Substances 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 238000001816 cooling Methods 0.000 description 7
- 239000011521 glass Substances 0.000 description 7
- 239000003365 glass fiber Substances 0.000 description 7
- 239000010445 mica Substances 0.000 description 7
- 229910052618 mica group Inorganic materials 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 229910045601 alloy Inorganic materials 0.000 description 6
- 239000000956 alloy Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229920003002 synthetic resin Polymers 0.000 description 6
- 239000000057 synthetic resin Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920001955 polyphenylene ether Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000004695 Polyether sulfone Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 229920006038 crystalline resin Polymers 0.000 description 2
- 238000007667 floating Methods 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- -1 metallic soaps Chemical compound 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 229920002492 poly(sulfone) Polymers 0.000 description 2
- 229920001230 polyarylate Polymers 0.000 description 2
- 229920002577 polybenzoxazole Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920006393 polyether sulfone Polymers 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical class N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 239000004419 Panlite Substances 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004693 Polybenzimidazole Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229920006127 amorphous resin Polymers 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- DMFGNRRURHSENX-UHFFFAOYSA-N beryllium copper Chemical compound [Be].[Cu] DMFGNRRURHSENX-UHFFFAOYSA-N 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001845 chromium compounds Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000005389 magnetism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920005575 poly(amic acid) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002480 polybenzimidazole Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 102220259718 rs34120878 Human genes 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Moulds For Moulding Plastics Or The Like (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、摺動特性に優れた強化
樹脂製CD−ROM機構部品の製造法に関する。詳しく
はCD(コンパクトディスク)を情報媒体として用いる
ゲーム機、音楽プレイヤー、コンピュータ、AV機器等
の機構部品の製造法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method of manufacturing a reinforced resin CD-ROM mechanism component having excellent sliding characteristics. More specifically, the present invention relates to a method of manufacturing mechanical parts such as a game machine, a music player, a computer and an AV device using a CD (compact disc) as an information medium.
【0002】[0002]
【従来の技術】近年、自動車、事務機、コンピュータ、
家電等の分野に於いて、板金、アルミダイキャストが用
いられていた部品の一部を軽量化、生産性、コストダウ
ンの目的から、樹脂製品で代替することが試みられてお
り、強化樹脂の需要が増加している。特にパソコン、ゲ
ーム機、音楽プレイヤーの需要拡大が著しく、CDを情
報媒体として用いるCD−ROM機の樹脂化が盛んに検
討されている。2. Description of the Related Art Recently, automobiles, office machines, computers,
In the field of home appliances, it has been attempted to replace some of the parts that used sheet metal and aluminum die casting with resin products for the purpose of weight reduction, productivity, and cost reduction. The demand is increasing. In particular, the demand for personal computers, game machines, and music players has expanded remarkably, and the use of resin for CD-ROM machines using CDs as information media has been actively studied.
【0003】トラバースベースシャーシ、メカシャー
シ、トレー等の樹脂製CD−ROM機構部品に要求され
る特性は、成形性、機械的特性、耐熱性、難燃性、寸法
精度、摺動特性である。このうち、摺動特性に関して、
強化充填剤及び/又は無機充填剤で強化した樹脂を射出
成形して得られたCD−ROM機構部品は、表面が粗面
となり、強化充填剤及び/又は無機充填剤の含量が多い
ものは著しく粗面となり、摺動性が悪くなるため、摺動
部分にグリースを塗布することが必須となっている。Characteristics required for resin CD-ROM mechanical parts such as a traverse base chassis, a mechanical chassis, and a tray are moldability, mechanical characteristics, heat resistance, flame retardancy, dimensional accuracy, and sliding characteristics. Of these, regarding sliding characteristics,
CD-ROM mechanical parts obtained by injection molding a resin reinforced with a reinforcing filler and / or an inorganic filler have a roughened surface, and those having a large content of the reinforcing filler and / or the inorganic filler are remarkably present. Since the surface becomes rough and slidability deteriorates, it is essential to apply grease to the sliding portion.
【0004】しかしながら、特に強化樹脂品と非強化樹
脂品の組み合わせ(例えば、メカシャーシが強化樹脂品
でトレーが非強化樹脂品の組み合わせ)に於いて、強化
樹脂品の強化充填剤及び/又は無機充填剤の浮きによる
粗面のため、非強化樹脂の表面が少しずつ削れる問題が
グリース塗布では解決することができず抜本的対策が求
められている。このような問題は、例えば、削り粉が光
学レンズ、CDに付着して読み取り障害の原因となった
り、削れにより、寸法的にくるいが生じ、摺動性に支障
をきたす原因となる。However, particularly in a combination of a reinforced resin product and a non-reinforced resin product (for example, a combination of a mechanical chassis with a reinforced resin product and a tray with a non-reinforced resin product), a reinforced filler and / or an inorganic material of the reinforced resin product. The problem that the surface of the non-reinforced resin is gradually scraped due to the rough surface due to the floating of the filler cannot be solved by grease application, and drastic measures are required. Such a problem causes, for example, shavings to be attached to the optical lens and the CD to cause a reading failure, or shaving causes a dimensional crease, which causes a problem in slidability.
【0005】そのため、強化樹脂成形品表面を平滑にす
るため、成形条件を種々変化させることが行われてい
る。成形されるときの要因の中で成形品表面の平滑に最
も大きな影響のあるのは金型温度であり、金型温度が高
いもの程好ましい。しかし、金型温度が高いと、可塑化
された樹脂の冷却固化に必要な冷却時間が長くなり成形
能率が下がる。Therefore, in order to make the surface of the reinforced resin molded product smooth, various molding conditions have been changed. Among the factors at the time of molding, it is the mold temperature that has the greatest effect on the smoothness of the surface of the molded product, and the higher the mold temperature, the more preferable. However, when the mold temperature is high, the cooling time required for cooling and solidifying the plasticized resin becomes long and the molding efficiency is lowered.
【0006】このため、金型温度を高くしないで表面の
再現性が良いもの、又、金型温度を高くしても冷却時間
が長くしなくてもよい樹脂製のCD−ROM機構部品が
要求されている。金型に加熱用、冷却用の孔をそれぞれ
とりつけておき交互に熱媒、冷媒を流して金型の加熱、
冷却を繰り返す方法も行われているきが、この方法は熱
の消費量も多く、冷却時間が長くなるという問題があっ
た。For this reason, there is a demand for a resin CD-ROM mechanism component which has good surface reproducibility without raising the die temperature and does not require a long cooling time even if the die temperature is raised. Has been done. Heating holes and cooling holes are attached to the mold, and heating medium and refrigerant are alternately flowed to heat the mold.
Although a method of repeating cooling is also used, this method has a problem that a large amount of heat is consumed and a cooling time becomes long.
【0007】[0007]
【発明が解決しようとする課題】本発明の目的は、摺動
特性が良好な強化樹脂製のCD−ROM機構部品の製造
法を提供しようとすることにある。SUMMARY OF THE INVENTION It is an object of the present invention to provide a method of manufacturing a CD-ROM mechanical component made of a reinforced resin having good sliding characteristics.
【0008】[0008]
【課題を解決するための手段】本発明は、強化充填剤及
び/又は無機充填剤を5〜50重量%含有する非結晶性
熱可塑性樹脂を、金属からなる主金型の金型キャビティ
を構成する型壁面のうち少なくとも摺動部を形成する型
壁面が、熱伝導率が0.002cal/cm・sec・
℃以下の耐熱性重合体からなる断熱層で0.01〜2m
m厚に被覆された金型を用いて射出成形するCD−RO
M機構部品の製造法である。DISCLOSURE OF THE INVENTION According to the present invention, a mold cavity of a main mold made of a metal is made of an amorphous thermoplastic resin containing 5 to 50% by weight of a reinforcing filler and / or an inorganic filler. At least the mold wall surface forming the sliding portion has a thermal conductivity of 0.002 cal / cm · sec ·
0.01-2m in heat insulation layer consisting of heat-resistant polymer below ℃
CD-RO injection-molded using m-thick mold
This is a method of manufacturing M mechanical parts.
【0009】以下、本発明について詳しく説明する。本
発明で用いられる強化充填剤としては、例えばガラス繊
維、炭素繊維、セラミックス繊維、金属繊維等の繊維強
化剤やガラスビーズ等の無機質粒体が挙げられる。無機
充填剤としては、ガラスフレーク、マイカ等の鱗片状の
無機充填剤、タルク、及びマグネシウム、アルミニウ
ム、ケイ素、カルシウム、カリウム、チタン等の酸化
物、炭酸塩、硅酸塩、硫酸塩などいずれの種類でも可能
である。Hereinafter, the present invention will be described in detail. Examples of the reinforcing filler used in the present invention include fiber reinforcing agents such as glass fibers, carbon fibers, ceramic fibers, and metal fibers, and inorganic particles such as glass beads. Examples of the inorganic filler include glass flakes, scale-like inorganic fillers such as mica, talc, and oxides such as magnesium, aluminum, silicon, calcium, potassium, titanium, carbonates, silicates, and sulfates. Types are also possible.
【0010】寸法精度、機械的特性のバランスからガラ
スフレーク、ガラスフレークとマイカの併用、ガラス繊
維とガラスフレークの併用、ガラス繊維とマイカの併
用、ガラス繊維とガラスフレーク、マイカの併用が良好
に使用できる。強化充填剤及び/又は無機充填剤の添加
量は、5〜50重量%(全組成物基準)で、この範囲で
必要に応じて選択できる。10〜40重量%配合された
組成物が、CD−ROM機構部品としての性能、成形性
の面からより好ましく使用できる。From the balance of dimensional accuracy and mechanical properties, glass flake, glass flake and mica combination, glass fiber and glass flake combination, glass fiber and mica combination, glass fiber and glass flake, mica combination are preferably used. it can. The amount of the reinforcing filler and / or the inorganic filler added is 5 to 50% by weight (based on the total composition), and can be selected as necessary within this range. A composition containing 10 to 40% by weight can be more preferably used in terms of performance and moldability as a CD-ROM mechanical component.
【0011】ガラス繊維は通常使用される直径のものが
使用でき、例えば5〜50μmの直径のものが好まし
い。特に好ましくは5〜15μmのガラス繊維である。
更に、強化充填剤又は無機充填剤と樹脂とは密着してい
る程、本発明のCD−ROM機構部品の摺動特性は良く
なり好ましい。樹脂の特性に応じて強化充填剤又は無機
充填剤と樹脂の密着性を良くするため、ビニルシラン、
アミノシラン、クロム化合物等の一般に使用される表面
処理剤で処理したものを良好に使用できる。As the glass fiber, those having a commonly used diameter can be used, and those having a diameter of, for example, 5 to 50 μm are preferable. Particularly preferably, the glass fiber is 5 to 15 μm.
Furthermore, the closer the reinforcing filler or inorganic filler and the resin are to each other, the better the sliding characteristics of the CD-ROM mechanism component of the present invention, which is preferable. In order to improve the adhesion between the reinforcing filler or the inorganic filler and the resin depending on the characteristics of the resin, vinylsilane,
Those treated with a commonly used surface treatment agent such as aminosilane and chromium compound can be favorably used.
【0012】ガラスフレークは、樹脂配合後の長径が1
000μm以下、好ましくは1〜500μmの範囲であ
り、且つアスペクト比(長径と厚みの比)が5以上、好
ましくは10以上、更に好ましくは30以上のものがよ
い。マイカは、例えばスドライト・マイカ(商標)
((株)クラレ製)等が良好に使用できる。樹脂配合後
の平均フレーク径が1000μm以下、好ましくは50
0μm以下、更に好ましくは200μm以下のものがよ
く、重量平均アスペクト比(フレークの平均直径/平均
厚み)は10以上、好ましくは30以上がよい。The glass flake has a major axis of 1 after blending with a resin.
It is 000 μm or less, preferably in the range of 1 to 500 μm, and has an aspect ratio (ratio of major axis and thickness) of 5 or more, preferably 10 or more, more preferably 30 or more. Mica is, for example, Sudrite Mica (trademark)
(Manufactured by Kuraray Co., Ltd.) can be used favorably. Average flake diameter after resin blending is 1000 μm or less, preferably 50
It is preferably 0 μm or less, more preferably 200 μm or less, and the weight average aspect ratio (average diameter of flakes / average thickness) is 10 or more, preferably 30 or more.
【0013】強化充填剤及び/又は無機充填剤を加える
非結晶性の熱可塑性樹脂としては、ポリスチレン、ゴム
変性ポリスチレン、AS樹脂、ABS樹脂などのポリス
チレン系樹脂、ポリカーボネイト樹脂、ポリカーボネイ
ト系アロイ樹脂(例えばABS樹脂とのアロイ樹脂)、
ポリフェニレンエーテル系樹脂(例えばゴム変性ポリス
チレン、ポリアミド樹脂、ポリオレフィンとのアロイ樹
脂)およびポリエーテルイミド、ポリスルホン、ポリア
リレート、ポリエーテルスルホンなどのエンジニアリン
グ樹脂等が良好に使用できる。As the amorphous thermoplastic resin to which the reinforcing filler and / or the inorganic filler is added, polystyrene, rubber-modified polystyrene, AS resin, polystyrene resin such as ABS resin, polycarbonate resin, polycarbonate alloy resin (for example, Alloy resin with ABS resin),
Polyphenylene ether resins (for example, rubber-modified polystyrene, polyamide resins, alloy resins with polyolefin) and engineering resins such as polyetherimide, polysulfone, polyarylate, and polyethersulfone can be favorably used.
【0014】本発明のCD−ROM機構部品に用いられ
る強化充填剤及び/又は無機充填剤で強化した樹脂とし
ては、低ソリグレードと称される強化樹脂が特に良好に
使用できる。これら合成樹脂に必要に応じてシリコーン
オイル(例えばジメチルシリコーン、メチルフェニルシ
リコーン、フッ素変性シリコーン等)、フッ素樹脂、二
硫化モリブデン等潤滑性物質を添加すると、本発明のC
D−ROM機構部品の摺動特性は更に向上し好ましい。As the resin reinforced with the reinforcing filler and / or the inorganic filler used in the CD-ROM mechanism component of the present invention, a reinforcing resin called low warp grade can be particularly favorably used. If a lubricating material such as silicone oil (eg, dimethyl silicone, methylphenyl silicone, fluorine-modified silicone, etc.), fluororesin, molybdenum disulfide, etc. is added to these synthetic resins as necessary, the C
The sliding characteristics of the D-ROM mechanism parts are further improved, which is preferable.
【0015】本発明で述べる非結晶性熱可塑性樹脂と
は、樹脂成分で非結晶性樹脂を50重量%以上から構成
してなる樹脂を言う。従って樹脂成分で50重量%未満
の結晶性樹脂を含むポリマーブレンド物、ポリマーアロ
イを含む。また、本発明のCD−ROM機構部品の樹脂
組成物は発明の効果を損なわない範囲でリン系、ブロム
系等の難燃剤、フェノール系、リン系、ヒンダードフェ
ノール系等の酸化防止剤、安定剤、酸化チタンやカーボ
ンブラック等の着色剤、金属セッケン等の滑剤、流動改
良剤、スチレン−ブタジエンブロック系、ポリエステル
アミド系等の補強用熱可塑性エラストマー等を所望量添
加できる。The non-crystalline thermoplastic resin described in the present invention means a resin composed of 50 wt% or more of non-crystalline resin as a resin component. Therefore, it includes a polymer alloy and a polymer alloy containing less than 50% by weight of a crystalline resin as a resin component. Further, the resin composition of the CD-ROM mechanism component of the present invention is a phosphorus-based or brominated flame retardant, a phenol-based, phosphorus-based, hindered phenol-based antioxidant, etc. Agents, colorants such as titanium oxide and carbon black, lubricants such as metallic soaps, flow improvers, reinforcing thermoplastic elastomers such as styrene-butadiene block-based and polyesteramide-based additives can be added in desired amounts.
【0016】本発明のCD−ROM機構部品の製造法に
用いる、金属からなる主金型は、鋼材、アルミニウム又
はアルミニウムを主成分とする合金、亜鉛合金、ベリリ
ウム−銅合金等の、一般的に合成樹脂の成形に使用され
ている金属金型を包含する。特に鋼材が良好に使用でき
る。本発明で断熱層に用いられる耐熱性重合体とは、ガ
ラス転移温度が150℃以上、好ましくは190℃以上
及び/又は融点が250℃以上、好ましくは280℃以
上の耐熱性重合体を言う。耐熱性重合体の熱伝導率は
0.002cal/cm・sec・℃以下であり、一般
の重合体はこの熱伝導率以下である。また、該耐熱重合
体の破壊伸度は10%以上の強靭な重合体が好ましい。
破壊伸度の測定法はASTM−D638に準じて行い、
測定時の引張り速度は5mm/分である。The main metal mold used in the method of manufacturing the CD-ROM mechanism component of the present invention is generally made of steel, aluminum or an alloy containing aluminum as a main component, zinc alloy, beryllium-copper alloy, or the like. It includes metal molds used for molding synthetic resins. Particularly, steel materials can be used favorably. The heat-resistant polymer used in the heat insulating layer in the present invention means a heat-resistant polymer having a glass transition temperature of 150 ° C or higher, preferably 190 ° C or higher and / or a melting point of 250 ° C or higher, preferably 280 ° C or higher. The heat conductivity of the heat resistant polymer is 0.002 cal / cm · sec · ° C. or less, and that of a general polymer is less than this heat conductivity. Further, a tough polymer having a fracture elongation of the heat resistant polymer of 10% or more is preferable.
The fracture elongation is measured according to ASTM-D638,
The tensile speed at the time of measurement is 5 mm / min.
【0017】本発明で断熱層として良好に使用される重
合体は、主鎖に芳香環を有する耐熱性重合体であり、特
に良好に使用されるものは有機溶剤に溶解する各種非結
晶性耐熱重合体、各種ポリイミドである。上記の非結晶
性耐熱重合体としては、ポリスルホン、ポリエーテルス
ルホン、ポリアリルスルホン、ポリアリレート、ポリフ
ェニレンエーテル、ポリベンツイミダゾール等が挙げら
れる。これ等の代表的な耐熱性重合体の繰り返し単位を
次に示す。The polymer which is preferably used in the present invention as the heat insulating layer is a heat resistant polymer having an aromatic ring in the main chain, and particularly preferably used are various amorphous heat resistant polymers which are soluble in an organic solvent. Polymers and various polyimides. Examples of the non-crystalline heat resistant polymer include polysulfone, polyether sulfone, polyallyl sulfone, polyarylate, polyphenylene ether, polybenzimidazole and the like. The repeating units of these typical heat resistant polymers are shown below.
【0018】[0018]
【化1】 Embedded image
【0019】[0019]
【化2】 Embedded image
【0020】[0020]
【化3】 Embedded image
【0021】[0021]
【化4】 [Chemical 4]
【0022】[0022]
【化5】 Embedded image
【0023】前記のポリイミドは各種あるが、直鎖型高
分子量ポリイミドが良好に使用される。一般に直鎖型高
分子量ポリイミドは破壊伸度が大きく、耐久性に優れて
いる。本発明で良好に使用される直鎖型の高分子量ポリ
イミドの例を表1に示した。なお、Tgはガラス転移温
度、又、nは繰り返し単位の数を表す。There are various kinds of the above-mentioned polyimides, but a linear high-molecular-weight polyimide is preferably used. Generally, the straight-chain high-molecular-weight polyimide has a large fracture elongation and excellent durability. Examples of linear type high molecular weight polyimides which are preferably used in the present invention are shown in Table 1. In addition, Tg represents a glass transition temperature, and n represents the number of repeating units.
【0024】[0024]
【表1】 [Table 1]
【0025】直鎖型高分子量ポリイミドは、構成成分に
よってTgが異なり、その例を表2及び表3に示した。
本発明に良好に使用される直鎖型の高分子量ポリイミド
のTgは、150℃以上が好ましく、更に好ましくは1
90℃以上、特に好ましくは230℃以上である。The linear type high molecular weight polyimides have different Tg depending on the constituents, and examples thereof are shown in Tables 2 and 3.
The Tg of the straight-chain high-molecular-weight polyimide used favorably in the present invention is preferably 150 ° C. or higher, more preferably 1
90 ° C or higher, particularly preferably 230 ° C or higher.
【0026】[0026]
【表2】 [Table 2]
【0027】[0027]
【表3】 [Table 3]
【0028】本発明で良好に使用される溶剤に溶解でき
る各種可溶性ポリイミドを表4に示す。Table 4 shows various soluble polyimides which can be dissolved in a solvent which is favorably used in the present invention.
【0029】[0029]
【表4】 [Table 4]
【0030】射出成形は、複雑な形状の成形品が一度の
成形で得られるところに経済的価値がある。この複雑な
金型表面を耐熱性重合体で被覆し、且つ強固に密着させ
ることが重要で、耐熱性重合体溶液及び/又は耐熱性重
合体前駆体溶液を塗布し、次いで加熱して耐熱性重合体
を形成させることが最も好ましい。従って、本発明で使
用される耐熱性重合体及び耐熱性重合体前駆体は、溶剤
に溶解できることが好ましい。Injection molding has economic value in that a molded product having a complicated shape can be obtained by molding once. It is important to coat the surface of this complicated mold with a heat-resistant polymer and firmly adhere to it. Apply a heat-resistant polymer solution and / or a heat-resistant polymer precursor solution, and then heat to heat resistance. Most preferably, a polymer is formed. Therefore, the heat resistant polymer and the heat resistant polymer precursor used in the present invention are preferably soluble in a solvent.
【0031】前記の非結晶性耐熱性重合体、可溶性ポリ
イミド及びポリイミド前駆体は、テトラヒドロフラン、
ジメチルフォルムアミド、ジメチルアセトアミド、N−
メチルピロリドン等の各種溶剤に溶解するものである。
直鎖型ポリイミド前駆体は、例えば芳香族ジアミンと芳
香族テトラカルボン酸二無水物を開環重付加反応させる
ことにより合成される。The above-mentioned non-crystalline heat-resistant polymer, soluble polyimide and polyimide precursor are tetrahydrofuran,
Dimethylformamide, dimethylacetamide, N-
It is soluble in various solvents such as methylpyrrolidone.
The linear polyimide precursor is synthesized, for example, by subjecting an aromatic diamine and an aromatic tetracarboxylic dianhydride to a ring-opening polyaddition reaction.
【0032】[0032]
【化6】 [Chemical 6]
【0033】これ等直鎖型ポリイミド前駆体は、加熱し
て脱水環化反応させることによりポリイミドを形成す
る。最も好ましい直鎖型ポリイミド前駆体は、ポリアミ
ド酸でありそり代表例の繰り返し単位と、それをイミド
化したポリイミドの繰り返し単位を次に示す。These linear polyimide precursors are heated to undergo a dehydration cyclization reaction to form a polyimide. The most preferable linear polyimide precursor is polyamic acid, and the repeating unit of a typical example of Sori and the repeating unit of a polyimide obtained by imidizing the same are shown below.
【0034】[0034]
【化7】 [Chemical 7]
【0035】[0035]
【化8】 Embedded image
【0036】[0036]
【化9】 [Chemical 9]
【0037】[0037]
【化10】 [Chemical 10]
【0038】上記のポリイミド前駆体のポリマーは、N
−メチルピロリドン等の溶媒に溶かし、金型壁面に塗布
される。これらの耐熱性重合体溶液、或いは耐熱性重合
体前駆体溶液には、コーティング時の粘度を調整した
り、溶液の表面張力を調整、チキソトロピー性を調整す
るための添加物を加えたり、金型との密着性を上げるた
めの微少の添加物を加えることができる。断熱層に使用
される耐熱性重合体について、非結晶性耐熱性重合体及
びポリイミドで説明したが、本発明は基本的にこれ等に
限定されるものではない。可とう性が付与されたエポキ
シ樹脂、シリコーン系樹脂等は成形条件等によっては使
用できる。The above polyimide precursor polymer is N
-Dissolve in a solvent such as methylpyrrolidone and apply it on the mold wall surface. To these heat-resistant polymer solutions or heat-resistant polymer precursor solutions, the viscosity at the time of coating, the surface tension of the solution, the additive for adjusting the thixotropy, or the mold may be added. It is possible to add a small amount of additive for improving the adhesion with the. Although the heat-resistant polymer used for the heat insulating layer has been described as the amorphous heat-resistant polymer and the polyimide, the present invention is not basically limited to these. Epoxy resin, silicone resin and the like having flexibility are usable depending on molding conditions.
【0039】本発明においては、耐熱性重合体皮膜と主
金型との密着力が大きいものを用い、更に好ましくは
0.8kg/10mm幅以上、特に好ましくは1kg/
10mm幅以上である。この密着力とは、密着した断熱
層を10mm幅に切り、接着面と直角方向に20mm/
分の速度で引張った時の剥離力である。この剥離力は測
定場所、測定回数によりかなりバラツキが見られるが、
最小値が大きいことが重要であり、安定して大きい剥離
力であることが好ましい。本発明に述べる密着力は金型
の主要部の密着力の最小値である。In the present invention, a material having a large adhesion between the heat resistant polymer film and the main mold is used, more preferably 0.8 kg / 10 mm width or more, particularly preferably 1 kg /
The width is 10 mm or more. This adhesive force means that the adherent heat insulating layer is cut into a width of 10 mm, and is 20 mm /
It is the peeling force when pulled at a speed of minutes. This peeling force varies considerably depending on the measurement location and the number of measurements, but
It is important that the minimum value is large, and stable and large peeling force is preferable. The adhesion force described in the present invention is the minimum value of the adhesion force of the main part of the mold.
【0040】ポリイミド等の断熱材の薄層の表面の平滑
性等を更に向上させるため、或いは表面の耐擦傷性を更
に向上させるため、或いは離型性を良くするため、ポリ
イミド層等の厚みの1/10位より薄い、別素材の材質
のものをポリイミド表面等に被覆したものを使用するこ
とも必要に応じてできる。この表面被覆物の別素材とし
ては、耐熱性樹脂の他に薄肉であれば各種金属も使用で
きる。また、合成樹脂のシートや型物の表面に、耐擦傷
性向上のために使用されている、一般にハードコートと
言われている塗料を塗布したものを使用することができ
る。また、例えば、熱硬化型のシリコーン系ハードコー
ト剤、特に、シリコーン系ハードコート剤にエポキシ系
物質を配合した密着性に優れたハードコート剤は、本発
明にとって好ましいものである。また、離型性を良くす
るためにフッ素樹脂やシリコーン系重合体を塗布したも
のを使用することも良好にできる。In order to further improve the smoothness of the surface of a thin layer of a heat insulating material such as polyimide, or to further improve the scratch resistance of the surface, or to improve the releasability, the thickness of the polyimide layer or the like is increased. If necessary, it is possible to use a material having a thickness of less than 1/10, which is made of another material, and coated on the polyimide surface or the like. As another material for the surface coating, various metals can be used in addition to the heat resistant resin as long as they are thin. Further, it is possible to use a synthetic resin sheet or mold surface coated with a coating generally called a hard coat, which is used for improving scratch resistance. Further, for example, a thermosetting type silicone hard coating agent, particularly a hard coating agent having excellent adhesion, which is a mixture of a silicone type hard coating agent and an epoxy type substance, is preferable for the present invention. It is also possible to favorably use a product coated with a fluororesin or a silicone-based polymer in order to improve releasability.
【0041】また、強化充填剤、無機充填剤の含量が多
くなると成形時に型表面の断熱層に傷がつきやすくな
り、この様な場合には、断熱層の上に耐擦傷性に優れた
硬質クロム等の金属層をつけたものを使用すると、良好
な摺動特性を有するCD−ROM機構部品が得られる。
金属からなる主金型キャビティを形成する型壁面を断熱
層で被覆した金型が用いられ射出成形されると、射出さ
れた合成樹脂自身の熱で型表面が加熱されながら成形さ
れる。従って、あたかも主金型の温度を高く設定して成
形されたのと同等の効果が得られる。成形品の型表面再
現性を良くし、成形品の平滑性を良くするには、射出さ
れた樹脂が型壁面に接して、少なくとも該樹脂に一定の
圧力が加わり型壁面に押しつけられるまでの微少の間だ
け、型表面温度が樹脂の軟化温度以上に保たれているこ
とが必要である。型壁面が断熱層で被覆された金型が用
いられると、断熱層の断熱効果により型表面が射出され
た樹脂の熱により加熱され、型表面再現性が良くなり、
成形品の平滑性は良くなる。When the content of the reinforcing filler and the inorganic filler is large, the heat insulating layer on the mold surface is easily scratched during molding. In such a case, the heat insulating layer is hard and has excellent scratch resistance. If a metal layer such as chrome is attached, a CD-ROM mechanical component having good sliding characteristics can be obtained.
When a mold in which a mold wall forming a main mold cavity made of metal is covered with a heat insulating layer is used for injection molding, the mold surface is heated by the heat of the injected synthetic resin itself. Therefore, it is possible to obtain the same effect as that obtained by molding by setting the temperature of the main mold high. In order to improve the mold surface reproducibility of molded products and the smoothness of molded products, it is necessary to keep the injected resin in contact with the mold wall surface, and at least a certain amount of pressure is applied to the resin to press it against the mold wall surface. Only during this period, it is necessary that the mold surface temperature be maintained above the softening temperature of the resin. When a mold in which the mold wall surface is covered with a heat insulating layer is used, the mold surface is heated by the heat of the injected resin due to the heat insulating effect of the heat insulating layer, improving mold surface reproducibility,
The smoothness of the molded product is improved.
【0042】本発明の摺動特性に優れるCD−ROM機
構部品は、少なくとも摺動部分に相当する金型壁面が上
記の断熱層で被覆された金型を用いて射出成形されるこ
とにより、強化充填剤または無機充填剤が配合された樹
脂成形品の強化充填剤または無機充填剤が成形品表面へ
のとび出しが少なくなっている。従って、金型壁面を被
覆する断熱層の厚みは、この目的を達成するだけの厚み
を必要とする。The CD-ROM mechanical component of the present invention having excellent sliding characteristics is reinforced by injection molding using a mold in which at least the mold wall surface corresponding to the sliding portion is covered with the above-mentioned heat insulating layer. Reinforcement filler or inorganic filler in a resin molded product containing a filler or an inorganic filler is less likely to protrude to the surface of the molded product. Therefore, the thickness of the heat insulating layer that covers the mold wall surface needs to be sufficient to achieve this purpose.
【0043】断熱層の厚みは、0.01〜2mmの範囲
で適度に選択される。好ましくは0.1〜0.5mmで
ある。0.01mm未満では効果が低く、2mmを越え
ることは不要である。厚み(cm)/熱伝導率(cal
/cm・sec・℃)値が、5〜100が本発明に特に
良好であり、この様に非常に狭い範囲が特に有効であ
る。5〜100の範囲より小さいと型表面再現性が悪く
なる傾向があり、この範囲より大きくなると、型内冷却
時間が長くなるが、或いは及び低熱伝導物質の鏡面状被
覆が困難になるなどの傾向を生ずることが多い。The thickness of the heat insulating layer is appropriately selected within the range of 0.01 to 2 mm. It is preferably 0.1 to 0.5 mm. If it is less than 0.01 mm, the effect is low, and if it exceeds 2 mm, it is unnecessary. Thickness (cm) / thermal conductivity (cal
/Cm.sec..degree. C.) value of 5 to 100 is particularly good for the present invention, and such a very narrow range is particularly effective. If it is smaller than the range of 5 to 100, the mold surface reproducibility tends to deteriorate, and if it is larger than this range, the cooling time in the mold tends to be long, and the mirror-like coating of the low thermal conductive material tends to be difficult. Often occurs.
【0044】本発明のCD−ROM機構部品では、主金
型温度が80℃以下に冷却され、射出された合成樹脂が
型表面に接触してから、少なくとも0.1秒の間、型表
面温度が100℃以上の状態で成形されることが好まし
い。主金型は更に好ましくは80℃以下、室温以上であ
る。一般に金型温度は80℃以下で射出成形されてお
り、80℃を越える高温にすると成形サイクルタイムが
長くなり、成形効率が低下する。また、室温より低くな
ると金型表面に結露が発生する。射出成形時の型表面温
度の変化は、合成樹脂組成物、主金型、断熱層の温度、
比熱、熱伝導率、密度から計算できる。例えばADIN
A及びADINAT(マサチューセッツ工科大学で開発
されたソフトウェア)等を用い、非線形有限要素法によ
る非定常熱伝導解析により計算できる。In the CD-ROM mechanical part of the present invention, the mold surface temperature is kept at least 0.1 seconds after the main mold temperature is cooled to 80 ° C. or less and the injected synthetic resin comes into contact with the mold surface. Is preferably molded at 100 ° C. or higher. The temperature of the main mold is more preferably 80 ° C. or lower and room temperature or higher. Generally, the mold temperature is 80 ° C. or less for injection molding, and if the mold temperature is higher than 80 ° C., the molding cycle time becomes long and the molding efficiency decreases. When the temperature is lower than room temperature, dew condensation occurs on the surface of the mold. The change of the mold surface temperature during injection molding is the temperature of the synthetic resin composition, the main mold, the heat insulating layer,
It can be calculated from specific heat, thermal conductivity, and density. For example ADIN
A and ADINAT (software developed at the Massachusetts Institute of Technology) and the like can be used to calculate by unsteady heat conduction analysis by the nonlinear finite element method.
【0045】本発明のCD−ROM機構部品の摺動部分
に相当する成形品の表面は、当然のことながら、平滑に
なる程、摺動抵抗が小さくなり、摺動性が良くなる。C
D−ROM機構部品は、機械的特性として一般に曲げ剛
性、引張り強さが大きい成形品が要求される。従って、
非結晶性樹脂に配合する強化充填剤及び/又は無機充填
剤の配合量は、一般に5〜50(全組成物基準)重量
%、好ましくは10〜40重量%である。これだけの強
化充填剤及び/又は無機充填剤を配合すると、通常の射
出成形では成形品表面が悪くなり、摺動性も悪くなる。As a matter of course, the smoother the surface of the molded product corresponding to the sliding portion of the CD-ROM mechanism component of the present invention, the smaller the sliding resistance and the better the slidability. C
The D-ROM mechanical component is generally required to be a molded product having high bending rigidity and tensile strength as mechanical properties. Therefore,
The amount of the reinforcing filler and / or the inorganic filler to be added to the amorphous resin is generally 5 to 50 (based on the total composition), preferably 10 to 40% by weight. If such a reinforcing filler and / or inorganic filler is blended, the surface of the molded product will be deteriorated by ordinary injection molding, and the slidability will be deteriorated.
【0046】本発明では、主金型は冷却されており、成
形品の少なくとも摺動部分に相当する型表面が断熱層で
被覆されている。加熱可塑化された強化充填剤又は無機
充填剤が断熱層で被覆された金型内に射出成形される
と、断熱層は射出された樹脂自身の熱で加熱され、主金
型の温度が高くされて成形した場合と同じ効果が得られ
る。即ち、断熱層が被覆された型キャビティ部分は成形
品表面にとび出した強化充填剤又は無機充填剤が大幅に
減った、平滑な成形品表面になる。In the present invention, the main mold is cooled, and the mold surface corresponding to at least the sliding portion of the molded product is covered with the heat insulating layer. When the heat-plasticized reinforcing filler or inorganic filler is injection-molded into the mold covered with the heat insulating layer, the heat insulating layer is heated by the heat of the injected resin itself, and the temperature of the main mold becomes high. The same effect as obtained by molding can be obtained. That is, the mold cavity portion covered with the heat insulating layer has a smooth molded product surface in which the reinforcing filler or the inorganic filler protruding to the surface of the molded product is significantly reduced.
【0047】本発明の製造法で得られるCD−ROM機
構部品は、少なくとも摺動部分に相当する部分に強化充
填剤又は無機充填剤が成形品表面に実質的にとび出して
いない表面を構成して成る、摺動特性に優れた射出成形
品である。本発明で得られるCD−ROM機構部品は、
少なくとも摺動特性が要求される部分に相当する金型壁
面を断熱層を被覆した金型を用いて成形される。摺動部
が成形品の凸部(金型の凹部)の場合、金型の凹部のみ
に断熱層が設けられることとなる。この場合、成形時の
ガス抜き用の細孔を金型の凹部に設けられることが好ま
しい。摺動部分以外も、必要に応じて(例えば良外観を
必要とする部分に)上述と同様の手段により平滑な表面
層を形成せしめることができる。The CD-ROM mechanism component obtained by the production method of the present invention has a surface in which the reinforcing filler or the inorganic filler does not substantially protrude from the surface of the molded product at least in the portion corresponding to the sliding portion. It is an injection molded product with excellent sliding characteristics. The CD-ROM mechanical component obtained by the present invention is
Molding is performed by using a mold in which a heat insulating layer is coated on the wall surface of the mold corresponding to at least the portion where sliding characteristics are required. When the sliding portion is the convex portion of the molded product (the concave portion of the mold), the heat insulating layer is provided only in the concave portion of the mold. In this case, it is preferable to provide pores for degassing at the time of molding in the concave portions of the mold. In addition to the sliding portion, a smooth surface layer can be formed as necessary (for example, a portion requiring a good appearance) by the same means as described above.
【0048】本発明に述べるCD−ROM機構部品と
は、CD(コンパクトディスク)、LD(レーザーディ
スク)、光磁気ディスク(MD(商標ミニディスク)
等)、光ディスク、FD(フロツピーディスク)、HD
(ハードディスク)等、ディスクを情報媒体として用
い、光又は磁気で書き込み、読み取りを行う機器、例え
ばコンピュータ、ゲーム機、音楽プレイヤー、AV機器
等の機構部品を総称して言う。The CD-ROM mechanical parts described in the present invention include CD (compact disc), LD (laser disc), and magneto-optical disc (MD (trademark mini disc).
Etc.), optical disc, FD (Floppy disc), HD
Mechanical components such as a (hard disk) that uses a disk as an information medium to write and read by light or magnetism, such as a computer, a game machine, a music player, and an AV device, are collectively referred to.
【0049】[0049]
【実施例】以下、実施例により本発明の強化充填剤樹脂
及び/又は無機充填剤を配合したCD−ROM機構部品
の摺動特性について詳細に説明する。表5に示す樹脂組
成物について下記の方法で行った。 (1)表面平滑性 平板の表面粗さをJIS−B0601に準じて(株)東
京精密製の三次元表面粗さ形状測定機サーコム570A
−3Dを用い、中心線平均粗さRaを測定した。 (2)摺動性 先端2.5mmR(先端径0.9mmφ)の径5mmφ
のピンを荷重2kgで平板試験片に押し付けながら、片
道距離10mmの距離を30mm/secの速度で10
000回往復運動させる摩擦・摩耗促進試験に於いて、
試験終了直前の摩擦係数、試験終了後のそれぞれの摩耗
量を摩耗深さで評価した。EXAMPLES The sliding characteristics of the CD-ROM mechanism component containing the reinforcing filler resin and / or the inorganic filler of the present invention will be described in detail below with reference to Examples. The resin composition shown in Table 5 was prepared by the following method. (1) Surface smoothness According to JIS-B0601, the surface roughness of a flat plate is a three-dimensional surface roughness profile measuring device, Surcom 570A manufactured by Tokyo Seimitsu Co., Ltd.
The center line average roughness Ra was measured using -3D. (2) Sliding property Diameter of 2.5mmR (tip diameter 0.9mmφ) 5mmφ
While pressing the pin of No. 2 against the flat plate test piece with a load of 2 kg, a one-way distance of 10 mm is applied at a speed of 30 mm / sec for 10 minutes.
In the friction / wear acceleration test of reciprocating 000 times,
The friction coefficient immediately before the end of the test and the amount of wear after the end of the test were evaluated by the wear depth.
【0050】[0050]
【実施例1〜3】次に示す主金型又はポリイミド被覆金
型を使用し、表5に示す樹脂組成物、組み合わせ、成形
条件にて、100mm×100mm×3mmtの平板試
験片及びピンを作成し、表面平滑性、摺動性を評価し
た。その結果を表5に示す。得られた成形品は、強化充
填剤、無機充填剤のとび出しが少なく、平滑な表面とな
り、摺動性も良好であった。 (a)主金型:鋼材(S55C)でつくられて平板金型
であり、型表面は鏡面状であり、更に硬質クロム鍍金が
施されている。 (b)ポリイミド前駆体及び硬化後のポリイミド:直鎖
型高分子量ポリイミド前駆体溶液は、トレーニース#3
00(東レ(株)製商品名)を用いた。硬化後のポリイ
ミドの性能は、Tgが300℃、熱伝導率が0.000
5cal/cm・sec・℃、破断伸度が60%。[Examples 1 to 3] Using the following main molds or polyimide-coated molds, 100 mm x 100 mm x 3 mmt flat plate test pieces and pins were prepared under the resin composition, combination and molding conditions shown in Table 5. Then, the surface smoothness and slidability were evaluated. The results are shown in Table 5. The obtained molded product had less protrusion of the reinforcing filler and the inorganic filler, had a smooth surface, and had good slidability. (A) Main mold: A flat plate mold made of steel (S55C), the mold surface is mirror-like, and hard chrome plating is applied. (B) Polyimide precursor and cured polyimide: The linear high-molecular-weight polyimide precursor solution was trained with # 3.
00 (trade name, manufactured by Toray Industries, Inc.) was used. The performance of the cured polyimide is Tg of 300 ° C. and thermal conductivity of 0.000.
5 cal / cm · sec · ° C, breaking elongation 60%.
【0051】(c)ポリイミド被覆金型:主金型にポリ
イミド前駆体溶液を塗布し、160℃に加熱して部分イ
ミド化し、次いで上記の塗布、160℃加熱を10回繰
り返し、最後に290℃まで加熱して100%イミド化
し、更に、ポリイミドの表面に、ポリジフェニルシロキ
サンとビスフェノールA系エポキシ樹脂を主成分とする
YP−9327(東芝シリコン(株)製商品名)を塗布
し、150℃で加熱硬化して、約2μm厚の重合体薄膜
を鏡面状に被覆した。 (d)強化樹脂及び未強化樹脂:ガラス繊維とマイカを
合計で30重量%配合したポリフェニレンエーテル系強
化樹脂としてザイロンX333V、未強化樹脂としてザ
イロン500V(旭化成工業(株)製 商品名)、ポリ
アセタール未強化樹脂としてテナック4520(旭化成
工業(株)製 商品名)、ABS未強化樹脂としてスタ
イラックIM15(旭加勢工業(株)製 商品名)、P
C/ABS強化樹脂としてノバロイ−S S5230
(ダイセル化学工業(株)製 商品名)及びPC樹脂と
してパンライトG−3130H(帝人化成(株)製 商
品名)を用いた。(C) Polyimide-coated mold: A polyimide precursor solution was applied to the main mold and heated to 160 ° C. for partial imidization, and then the above-mentioned coating and heating at 160 ° C. were repeated 10 times, and finally 290 ° C. It is heated up to 100% for imidization, and further, YP-9327 (trade name of Toshiba Silicon Co., Ltd.) containing polydiphenylsiloxane and bisphenol A epoxy resin as main components is applied on the surface of the polyimide, and at 150 ° C. After heat curing, a polymer thin film having a thickness of about 2 μm was mirror-coated. (D) Reinforced resin and unreinforced resin: Zylon X333V as a polyphenylene ether-based reinforced resin containing glass fiber and mica in a total amount of 30% by weight, Zylon 500V as an unreinforced resin (trade name of Asahi Kasei Kogyo Co., Ltd.), and polyacetal Tenac 4520 (a product name of Asahi Kasei Kogyo Co., Ltd.) as a reinforced resin, Stylac IM15 (a product name of Asahi Kase Kogyo Co., Ltd.) as an ABS unreinforced resin, P
Novalloy-S S5230 as C / ABS reinforced resin
(Trade name manufactured by Daicel Chemical Industries, Ltd.) and Panlite G-3130H (trade name manufactured by Teijin Chemicals Ltd.) were used as the PC resin.
【0052】[0052]
【比較例1〜3】ポリイミド被覆をしない金型を用いる
以外は、実施例1〜3と同様に試験を行った。その結果
を表5に示す。得られた成形品は、強化充填剤、無機充
填剤のとび出しが多く、表面平滑性は悪く、摺動特性も
悪かった。特にピンの摩耗が大きかった。[Comparative Examples 1 to 3] Tests were conducted in the same manner as in Examples 1 to 3 except that a mold not coated with polyimide was used. The results are shown in Table 5. The obtained molded product had a large amount of protrusion of the reinforcing filler and the inorganic filler, poor surface smoothness, and poor sliding characteristics. In particular, the pins were heavily worn.
【0053】[0053]
【表5】 [Table 5]
【0054】[0054]
【発明の効果】従来、強化樹脂製CD−ROM機構部品
の問題であった、強化充填剤、無機充填剤の浮きによる
粗面のため摺動部が削れて削れ粉が発生する問題、摺動
部の寸法がガタつく問題が解決された、優れた摺動特性
を有するCD−ROM機構部品を提供することを可能に
する。EFFECTS OF THE INVENTION Conventionally, the problem of the reinforced resin CD-ROM mechanism parts, that is, the problem that the sliding portion is scraped off due to the rough surface due to the floating of the reinforcing filler and the inorganic filler, and the sliding, (EN) It is possible to provide a CD-ROM mechanical component having excellent sliding characteristics, in which the problem of rattling of the size of a part is solved.
Claims (1)
50重量%含有する非結晶性熱可塑性樹脂を、金属から
なる主金型の金型キャビティを構成する型壁面のうち少
なくとも摺動部を形成する型壁面が、熱伝導率が0.0
02cal/cm・sec・℃以下の耐熱性重合体から
なる断熱層で0.01〜2mm厚に被覆された金型を用
いて射出成形するCD−ROM機構部品の製造法。1. A reinforcing filler and / or an inorganic filler is used in an amount of 5 to 5.
The amorphous thermoplastic resin containing 50% by weight has a thermal conductivity of 0.0 at least on the mold wall surface forming the sliding portion among the mold wall surfaces constituting the mold cavity of the main mold made of metal.
A method for producing a CD-ROM mechanical component, which is injection-molded using a mold covered with a heat insulating layer made of a heat-resistant polymer having a thickness of 02 cal / cm · sec · ° C. or less to a thickness of 0.01 to 2 mm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25696794A JPH08118433A (en) | 1994-10-21 | 1994-10-21 | Manufacture of reinforced resin cd-rom mechanism member excellent in sliding characteristic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25696794A JPH08118433A (en) | 1994-10-21 | 1994-10-21 | Manufacture of reinforced resin cd-rom mechanism member excellent in sliding characteristic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08118433A true JPH08118433A (en) | 1996-05-14 |
Family
ID=17299864
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25696794A Pending JPH08118433A (en) | 1994-10-21 | 1994-10-21 | Manufacture of reinforced resin cd-rom mechanism member excellent in sliding characteristic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08118433A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013132866A (en) * | 2011-12-27 | 2013-07-08 | Hoya Corp | Method for producing plastic lens |
-
1994
- 1994-10-21 JP JP25696794A patent/JPH08118433A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013132866A (en) * | 2011-12-27 | 2013-07-08 | Hoya Corp | Method for producing plastic lens |
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