JPS6258447B2 - - Google Patents
Info
- Publication number
- JPS6258447B2 JPS6258447B2 JP18348281A JP18348281A JPS6258447B2 JP S6258447 B2 JPS6258447 B2 JP S6258447B2 JP 18348281 A JP18348281 A JP 18348281A JP 18348281 A JP18348281 A JP 18348281A JP S6258447 B2 JPS6258447 B2 JP S6258447B2
- Authority
- JP
- Japan
- Prior art keywords
- metal
- hydrolyzing
- patterning
- substrate
- film obtained
- 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
- 239000000758 substrate Substances 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 239000002184 metal Substances 0.000 claims description 13
- 238000007772 electroless plating Methods 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 238000000059 patterning Methods 0.000 claims description 7
- 229920003023 plastic Polymers 0.000 claims description 7
- 230000003301 hydrolyzing effect Effects 0.000 claims description 6
- 150000002736 metal compounds Chemical class 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- 229910052732 germanium Inorganic materials 0.000 claims description 2
- 229910052738 indium Inorganic materials 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 229910052715 tantalum Inorganic materials 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000003700 epoxy group Chemical group 0.000 claims 1
- 229910052733 gallium Inorganic materials 0.000 claims 1
- 229910052735 hafnium Inorganic materials 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- 229910052720 vanadium Inorganic materials 0.000 claims 1
- 229910052726 zirconium Inorganic materials 0.000 claims 1
- 239000011347 resin Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 238000005530 etching Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 101150003085 Pdcl gene Proteins 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- 229920002574 CR-39 Polymers 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- 229910018104 Ni-P Inorganic materials 0.000 description 1
- 229910018536 Ni—P Inorganic materials 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01D—MEASURING NOT SPECIALLY ADAPTED FOR A SPECIFIC VARIABLE; ARRANGEMENTS FOR MEASURING TWO OR MORE VARIABLES NOT COVERED IN A SINGLE OTHER SUBCLASS; TARIFF METERING APPARATUS; MEASURING OR TESTING NOT OTHERWISE PROVIDED FOR
- G01D5/00—Mechanical means for transferring the output of a sensing member; Means for converting the output of a sensing member to another variable where the form or nature of the sensing member does not constrain the means for converting; Transducers not specially adapted for a specific variable
- G01D5/26—Mechanical means for transferring the output of a sensing member; Means for converting the output of a sensing member to another variable where the form or nature of the sensing member does not constrain the means for converting; Transducers not specially adapted for a specific variable characterised by optical transfer means, i.e. using infrared, visible, or ultraviolet light
- G01D5/32—Mechanical means for transferring the output of a sensing member; Means for converting the output of a sensing member to another variable where the form or nature of the sensing member does not constrain the means for converting; Transducers not specially adapted for a specific variable characterised by optical transfer means, i.e. using infrared, visible, or ultraviolet light with attenuation or whole or partial obturation of beams of light
- G01D5/34—Mechanical means for transferring the output of a sensing member; Means for converting the output of a sensing member to another variable where the form or nature of the sensing member does not constrain the means for converting; Transducers not specially adapted for a specific variable characterised by optical transfer means, i.e. using infrared, visible, or ultraviolet light with attenuation or whole or partial obturation of beams of light the beams of light being detected by photocells
- G01D5/347—Mechanical means for transferring the output of a sensing member; Means for converting the output of a sensing member to another variable where the form or nature of the sensing member does not constrain the means for converting; Transducers not specially adapted for a specific variable characterised by optical transfer means, i.e. using infrared, visible, or ultraviolet light with attenuation or whole or partial obturation of beams of light the beams of light being detected by photocells using displacement encoding scales
- G01D5/34707—Scales; Discs, e.g. fixation, fabrication, compensation
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optical Transform (AREA)
- Transmission And Conversion Of Sensor Element Output (AREA)
Description
【発明の詳細な説明】
本発明は透明プラスチツク基板上に金属化合物
混合物を加水分解して得られる被膜上に無電メツ
キによつてパターニング又は、紫外線露光による
選択的無電解メツキによつて形状パターニングし
たことを特徴とするエンコーダスリツト板に関す
る。DETAILED DESCRIPTION OF THE INVENTION The present invention involves patterning a film obtained by hydrolyzing a metal compound mixture on a transparent plastic substrate by electroless plating or by selective electroless plating using ultraviolet light exposure. The present invention relates to an encoder slit plate characterized by the following.
従来、エンコーダスリツト板は金属のエツチン
グ又は、ガラス基板にクロム蒸着によりクロム被
膜を形成し、目的とする形状にパターニングする
ことによつて作られていた。しかし金属エツチン
グの場合、スリツト穴径の微細エツチングには、
限度があり、高分解機能を有するエンコーダとし
ては限度があつた。又、ガラス上にクロム蒸着し
て得られた金属クロム膜を目的とする形状にパタ
ーニングすることによつて作られたエンコーダス
リツト板は一度に大量又は大表面積のものを作る
ことができず、また真空設備を使用することから
もコストダウンが困難であつた。またプラスチツ
ク透過率の大きいエンコーダスリツト板として
は、適材のアクリル樹脂板を用いた場合、通常で
は無電解メツキが被覆されないため、蒸着を用い
ることになる。結局ガラス基板と同様の欠点を有
する。現在使用されているプラスチツクの中でア
クリル、メタクリル系樹脂は機械的性質にすぐ
れ、美感を満足させるものであるが金属あるいは
その他の無機物質材料にくらべ耐摩耗性、表面硬
度、耐熱性あるいは耐薬品性に劣つている、比較
的耐摩耗性に優れている樹脂としてジエチレング
リコールビスアクリルカーバイト樹脂があるがこ
の樹脂の耐摩耗性、表面硬度も実用上必ずしも十
分と言えない。 Conventionally, encoder slit plates have been made by forming a chromium coating on a glass substrate by etching metal or vapor depositing chromium, and patterning it into a desired shape. However, in the case of metal etching, fine etching with a slit hole diameter requires
There were limitations as an encoder with a high resolution function. Furthermore, encoder slit plates made by patterning a metallic chromium film obtained by vapor deposition of chromium on glass into a desired shape cannot be made in large quantities or with a large surface area at one time; Furthermore, it has been difficult to reduce costs due to the use of vacuum equipment. Furthermore, when an appropriate acrylic resin plate is used as the encoder slit plate with high plastic transmittance, vapor deposition is used because electroless plating is not normally covered. After all, it has the same drawbacks as a glass substrate. Among the plastics currently used, acrylic and methacrylic resins have excellent mechanical properties and are aesthetically pleasing, but compared to metals and other inorganic materials, they have poor wear resistance, surface hardness, heat resistance, and chemical resistance. Diethylene glycol bisacrylic carbide resin is a resin that has relatively excellent abrasion resistance but has poor properties, but the abrasion resistance and surface hardness of this resin are not necessarily sufficient for practical use.
本発明はかかる欠点を除去したもので、その目
的はガラスに比べ、機械加工、成形しやすい透明
プラスチツク基板を用いて、その上に金属化合物
混合物を加水分解して得られる被膜を設け紫外線
露光による選択的無電解メツキによつて形状パタ
ーニングしたことによりエンコーダスリツトの微
細パターンが可能となり又、真空装置を用いない
ことでコストダウン、大面積、大量生産ができ
る、さらに紫外線露光による選択メツキ方法を用
いた場合、工程短縮、品質向上となることを示す
ものである。 The present invention eliminates such drawbacks, and its purpose is to use a transparent plastic substrate that is easier to machine and mold than glass, and to provide a coating obtained by hydrolyzing a metal compound mixture thereon, which is then exposed to ultraviolet light. By patterning the shape using selective electroless plating, it is possible to create fine patterns for encoder slits, and by not using vacuum equipment, costs can be reduced, large areas can be produced, and mass production can be achieved.Additionally, a selective plating method using ultraviolet light exposure has been developed. This shows that when used, the process can be shortened and quality can be improved.
本発明に用いられる基板としては、光透過性基
板なら何でもかまわないが平面の平滑性、透過
率、熱膨張係数の低さなどからアクリル樹脂、ポ
リエステル、ポリカードネート樹脂、CR―39樹
脂、レポリマー樹脂、ポリサルフオン樹脂、ポリ
エーテルサルフオン樹脂、スピラン樹脂等があ
る。基板としては100μ〜数mm厚のものが用いら
れる。これらのプラスチツク基板に無電解メツキ
を可能にし、密着性を向上させ、しかも、基板を
さらに金属に硬度、及び膨張係数を近づけ、熱膨
張による金属とプラスチツクの応力を緩和し、ひ
ずみによるクラツクの発生を防ぐために、プラス
チツク基板上にRM(OCnH2o+1)x(R:アルキル
基、又はアルキル基にエポキシ基、アミノ基等を
少なくとも含む、M:Ti,Si,Zr,Hf,V,
Nb,Ta,Co,Al,Ge,Inから選ばれた金属、
x:金属の価数を考慮した整数値、n:整数)か
らなる金属化合物混合物を加水分解して得られる
被膜を形成しておき、通常の無電解メツキ用前処
理液(センシタイザー、アクテイベーター)で処
理した後、無電解メツキ金属被覆したので光感光
性レジストを塗布して紫外露光により目的の形状
にパターニングを行い、不必要部のレジストをエ
ツチングし、金属エツチングしたのち、レジスト
エツチングしてパターニングする、又は紫外線露
光による選択的無電解メツキ方法は、
(1) 先に述べたコート基板をSnCl2(HCl酸性)
溶液に浸漬し、数分後乾燥する。 The substrate used in the present invention may be any light-transmissive substrate, but due to its smoothness, transmittance, and low coefficient of thermal expansion, acrylic resin, polyester, polycarbonate resin, CR-39 resin, repolymer resin, etc. There are resins, polysulfone resins, polyethersulfone resins, spiran resins, etc. The substrate used is one with a thickness of 100 μm to several mm. It enables electroless plating on these plastic substrates, improves adhesion, and also brings the substrate closer to metal in hardness and coefficient of expansion, alleviating stress between metal and plastic due to thermal expansion and preventing cracks caused by strain. In order to prevent this, RM(OCnH 2o+1 )
Metal selected from Nb, Ta, Co, Al, Ge, In,
A film obtained by hydrolyzing a metal compound mixture consisting of x: an integer value taking into account the valence of the metal, and n: an integer is formed, and a film obtained by hydrolyzing a metal compound mixture consisting of ) After processing with electroless plating metal coating, a photosensitive resist was applied and patterned into the desired shape by ultraviolet exposure, the resist was etched in unnecessary areas, metal etching was performed, and then resist etching was performed. The selective electroless plating method by patterning or UV exposure is as follows: (1) The coated substrate described above is coated with SnCl 2 (HCl acidic).
Dip into the solution and dry after a few minutes.
(2) 基板にセキエイガラスを用いたフオトマスク
を密着し、2600Å以下の波長をもつ紫外線を適
度の時間をもつて照射する。(2) A photomask made of Sekiei glass is closely attached to the substrate, and ultraviolet light with a wavelength of 2600 Å or less is irradiated for an appropriate amount of time.
(3) PdCl2(HCl酸性)溶液に基板を浸漬し、水
洗後、無電解ニツケル浴に数分間入れ、メツキ
する。(3) Immerse the substrate in PdCl 2 (acidic HCl) solution, rinse with water, and then place in an electroless nickel bath for several minutes to plate.
(2)の紫外線によりSn2+U,VSn4+となり、
(3)のPdCl2の溶液の浸漬により非露光部の反応
はSn2++Pd2+→Sn4++Pd0となりそのパラジウム
金属にニツケルが析出すると考えられる。また紫
外露光部はSn4+となつているためPd2+を還元す
ることは不可能である。それゆえニツケルが析出
されない。 The ultraviolet light in (2) turns into Sn 2+ U, VSn 4+ , and the reaction in the non-exposed area becomes Sn 2+ + Pd 2+ → Sn 4+ + Pd 0 by immersion in the PdCl 2 solution in (3), and the palladium metal changes. It is thought that nickel is precipitated. Furthermore, since the UV-exposed area is Sn 4+ , it is impossible to reduce Pd 2+ . Therefore, nickel is not deposited.
メツキは硬さ及び密着性、安価を考慮に入れ
Ni―Pを使用した。メツキ厚は300Å〜1μm程
度であり、エンコーダスリツト板の場合、スリツ
トサイドエツジがしつかりでていれば多少のピン
ホールは問題とならないので1000Å〜3000Åあれ
ば十分である。このようにして得られたエンコー
ダスリツト板は微細パターンが可能であり、作成
にあつての低コスト化、工程短縮、もみのがせな
い。さらにレジストなどを用いないので品質向上
にもつながる。 We take into consideration hardness, adhesion, and low price for the metal fittings.
Ni-P was used. The plating thickness is about 300 Å to 1 μm, and in the case of an encoder slit plate, a pinhole of 1000 Å to 3000 Å is sufficient as a few pinholes will not be a problem as long as the slit side edges are firm. The encoder slit plate obtained in this way can be formed into a fine pattern, and the manufacturing cost can be reduced, the process can be shortened, and the plate cannot be rubbed out. Furthermore, since no resist is used, quality can be improved.
実施例 1
アクリル基板上に、
TMS(6部)、イソプロピルアルコール(10部)
0.05NHCl(2部)触媒としてSnCl2を入れ混合撹
拌した後、還流しある程度硬化させておき、デイ
ツピング法又はスピンナー法により塗布した後70
℃程度で3h乾燥硬化させた10NNaOHで浸漬後十
分水洗しメツキした。このコートは非常によく
Sn2+を吸着し、メツキの密着性も良好であつ
た。メツキ工程は前述による。Example 1 On an acrylic substrate, TMS (6 parts), isopropyl alcohol (10 parts)
0.05NHCl (2 parts) Add SnCl 2 as a catalyst, mix and stir, reflux and cure to some extent, apply by dipping method or spinner method, and then apply for 70 minutes.
After soaking in 10N NaOH which was dried and cured at about ℃ for 3 hours, it was thoroughly washed with water and plated. this coat is very well
It adsorbed Sn 2+ and had good plating adhesion. The plating process is as described above.
実施例 2
アクリル板上に勝田化工KK製の
NIKCOATA430(主剤)93部Z―102(触媒Z―
102)7部を混合撹拌し、脱胞したのち、デイツ
ピング又はスピナー塗布した。乾燥硬化は、70℃
3hrで行つた。以下の工程は実施例1と同様であ
る。Example 2 Katsuta Kako KK made on acrylic board
NIKCOATA430 (base agent) 93 parts Z-102 (catalyst Z-
102) 7 parts were mixed and stirred to remove the cells, and then applied by dipping or spinner coating. Dry curing at 70℃
I went there in 3 hours. The following steps are the same as in Example 1.
実施例 3
アクリル板上にH2N―
CH2CH2NHCH2CHCH2Si(OCH3)3(東芝シリコ
ン製SH6020)5部、A―430(勝田化工製)5部
を混合撹拌し、脱胞したのちデイツピング又はス
ピンナー法で塗布した。乾燥温度は70℃3hrで行
つた。以下の工程は実施例1と同様である。Example 3 H 2 N on an acrylic plate
5 parts of CH 2 CH 2 NHCH 2 CHCH 2 Si(OCH 3 ) 3 (SH6020 manufactured by Toshiba Silicon) and 5 parts of A-430 (manufactured by Katsuta Kako) were mixed and stirred, and after defoaming, coating was performed by dipping or spinner method. The drying temperature was 70°C for 3 hours. The following steps are the same as in Example 1.
実施例 4
実施例1,2,3のアクリル板をポリカーボネ
イトにおいても実験した。Example 4 The acrylic plates of Examples 1, 2, and 3 were also tested on polycarbonate.
Claims (1)
(OCnH2o+1)x(R:アルキル基、又はアルキル基
にエポキシ基アミノ基等を少なくとも含む、M:
Ti,Si,Zr,Hf,V,Nb,Ta,Co,Al,Ge,
Ga,Inから選ばれた金属、x:金属の価数を考
慮した整数値、n:整数)からなる金属化合物、
混合物を加水分解して得られる被膜を形成してお
き、紫外線露光による選択的無電解メツキによつ
て形状パターニングしたことを特徴とするエンコ
ーダスリツト板の製造方法。 2 特許請求の範囲第1項に示した金属化合物、
混合物を加水分解して得られた被膜上に目的の形
状にパターニングすることを特徴とするエンコー
ダスリツト板の製造方法。[Claims] 1. RM on a transparent plastic substrate
(OCnH 2o+1 ) x (R: an alkyl group, or an alkyl group containing at least an epoxy group, an amino group, etc., M:
Ti, Si, Zr, Hf, V, Nb, Ta, Co, Al, Ge,
A metal compound consisting of a metal selected from Ga, In, x: an integer value considering the valence of the metal, n: an integer),
1. A method for manufacturing an encoder slit plate, comprising forming a film obtained by hydrolyzing a mixture, and patterning the film by selective electroless plating using ultraviolet light exposure. 2. The metal compound shown in claim 1,
A method for producing an encoder slit plate, which comprises patterning a desired shape on a film obtained by hydrolyzing a mixture.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18348281A JPS5885112A (en) | 1981-11-16 | 1981-11-16 | Manufacture of encoder slit plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18348281A JPS5885112A (en) | 1981-11-16 | 1981-11-16 | Manufacture of encoder slit plate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5885112A JPS5885112A (en) | 1983-05-21 |
JPS6258447B2 true JPS6258447B2 (en) | 1987-12-05 |
Family
ID=16136577
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18348281A Granted JPS5885112A (en) | 1981-11-16 | 1981-11-16 | Manufacture of encoder slit plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5885112A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4397635B2 (en) * | 2003-07-03 | 2010-01-13 | 株式会社根本杏林堂 | Controller device, controller unit and chemical solution injection device |
JP5846686B2 (en) | 2011-11-22 | 2016-01-20 | 株式会社ミツトヨ | Method for manufacturing scale of photoelectric encoder |
-
1981
- 1981-11-16 JP JP18348281A patent/JPS5885112A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5885112A (en) | 1983-05-21 |
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