JPH044656B2 - - Google Patents
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- JPH044656B2 JPH044656B2 JP59085656A JP8565684A JPH044656B2 JP H044656 B2 JPH044656 B2 JP H044656B2 JP 59085656 A JP59085656 A JP 59085656A JP 8565684 A JP8565684 A JP 8565684A JP H044656 B2 JPH044656 B2 JP H044656B2
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- polishing
- crystallized glass
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- polished
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Description
[技術分野]
本発明は磁気デイスク用・結晶化ガラス基板表
面を精密研摩仕上げして成る磁気デイスク用基板
の製造方法に関する。
[技術的背景]
一般に磁気デイスク用基板としては、次の様な
特性が要求される。
(1) 0.3μm以下の低ヘツド浮上高さに伴い磁気ヘ
ツドの安定な浮上と記録特性の安定性を得るた
め研摩後の表面粗度が良好なこと。
(2) 基板表面に形成される磁性薄膜の欠陥の要因
となる突起や孔状へこみがないこと。
(3) 機械加工、研摩、或いは使用時の高速回転に
十分耐える機械的強度を有すること。
(4) 耐食性、耐候性、且つ耐熱性を有すること。
従来磁気デイスク用基板にはAl合金が使用さ
れているが、Al合金基板では材料の結晶異方性、
材料欠陥及び材料中に存在する非金属介在物等の
ため機械加工や研摩工程において、これらが基板
表面に突起として残存したり或いは、結晶化され
た部分がスポツト状に脱落して凹みを生じ充分な
研摩を行なつても表面粗度は、せいぜい200Å程
度であり、突起や凹み、うねりのある表面状態で
高密度磁気記録用デイスク用基板材としては十分
でない。
現在スパツタデイスク用基板材の表面状態を改
善する目的として、Al合金表面にアルマイト層
を形成し硬度を増加して研摩加工性を向上するた
めの方法がとられているが、アルマイト形成中に
Al合金中の微量不純物(Fe、Mn、Si)が金属間
化合物として析出するため、アルマイト処理後そ
の部分が凹みの欠陥の発生要因となる。母材合金
の高純度化を図ることは製造プロセス上至難に近
く、さらにAl合金の場合耐食性、清浄度の面で
も取りあつかいが問題となつている。またスパツ
タリングやメツキによる薄膜磁気記録媒体形成の
場合、Al合金と磁性膜の化学反応や拡散の問題
が生じ、さらに工程により磁性膜に熱処理を加え
る必要があるが、Al合金基板は基板が変形し易
く、形状精度が悪くなると共に面振れ加速度は上
昇するため、熱処理することは困難である。
なお、Al基板上にSiO2、Al2O3等の酸化物をス
パツタリングにより形成する方法もあるが、Al
基板とスパツタ形成後の密着力が弱いという欠点
がある。
一般に磁気デイスク基板の加工の良否は、その
まま、磁気デイスクのランアウト、加速度成分、
磁気記録媒体の信号エラー等に依存する。ところ
でAl合金の場合はメタル材の為ビツカース硬度
も100程度(セラミツクの場合600以上)であり、
曲げ強度も1000Kg/cm2(セラミツクの場合4000
Kg/cm2以上)であつて、高密度記録になるに従つ
てスラツチ、キズ、平坦度、うねりなどの形状精
度もきびしくなつてきており加工は一層困難とな
つてきている。砥粒加工の際も砥粒がつめ込まれ
やすく欠陥となる。
またAl合金基板の場合、表面の耐食性、耐候
性、汚染を防ぐこと、旋削工程、ポリツシング工
程、保管の際、清浄度、防錆、汚れ等、製造工程
上充分な配慮が必要となつている。
[目的]
本発明は、上述の諸欠点、問題を解消する新規
な磁気デイスク用基板の製造方法を提供すること
を基本目的とし、特に、従来高精度加工の困難さ
のために用いることが出来なかつた結晶化ガラス
を磁気デイスク用基板材料として有効に用いるこ
とを課題とする。
[発明の構成概要]
本発明は結晶化ガラス基板表面上に形成する被
着磁性膜の特性向上、信頼性を保障するために表
面粗度を80Å以下に精密研摩仕上げをした磁気デ
イスク用基板の製造方法を特徴とする。
すなわち、本発明の磁気デイスク用基板の製造
方法は、単位体積当りの表面積が130m2/g以下
で、形状が実質的に球状の粒径320Å以下の無水
アルミナ微粉末を純水中に懸濁させた液を研摩液
とし、該研摩液中で被研摩結晶化ガラスとラツプ
盤を対向させて、ラツプ荷重0.1〜2Kg/cm2を加
えながら精密研摩することを特徴とする。
[発明の開示]
結晶化ガラス基板の場合は、Al合金に比べ機
械的強度も強く砥粒加工での形状精度の管理も比
較的容易となる。さらに耐食性、耐候性に特別配
慮する必要もなく、表面の汚染も絶縁薄膜をスパ
ツタリングにより形成する際スパツタクリーニン
グにより表面の清浄化を行うことができる。
またAl合金を旋削加工した際、表面には加工
変質層が残留しているのに対して結晶化ガラスの
場合はメカノケミカルポリツシユ仕上げにより表
面がバルクでの応力歪との差異はなく、基板にコ
ーテイングされる媒体への歪の転写はない。
今日結晶化ガラスが、Al合金基板に比べ耐熱
性、耐摩耗性、耐候性、絶縁性及び機械的強度の
すぐれていることより各種分野に広範囲の用途に
使用されるようになつたが、基板表面に薄膜媒体
処理の施される磁気デイスク用基板では、媒体の
高密度化に伴つて基板表面の平滑性、無歪基板の
必要性に迫まられている。磁気デイスク用基板に
使用する場合は表面微細欠陥によるドロツプアウ
トの発生や、ヘツドクラツシユ等、信頼性を損う
という問題があり、結晶化ガラスを磁気デイスク
用基板として用いることには従来なお多くの克服
すべき困難があつた。
従来、結晶化ガラスの精密研摩方法として、フ
オトマスク、レンズ等に適用されていた溶融型非
晶質ガラス研摩法が採用されていた。この研摩方
法は、酸化セリウムやベンガラを砥粒とし、レン
ズ等の表面を50Å以下の粗度に仕上げることがで
きる。ところが、結晶化ガラスに適用しても、材
質が実質的に結晶化されているため、研摩面に微
細突起や凹部が生成し、250Å程度の表面粗度し
か得られない問題があつた。
そのために、本発明者等は、結晶化ガラスの高
精度表面研摩の方法を開発し先に特許出願した
(特願昭58−155176〜155178)。即ち、これらは薄
膜磁気ヘツド用の結晶化ガラス基板表面を表面粗
度50Å以下に精密研摩仕上する研摩方法に関す
る。本発明はさらにその方法を磁気デイスク用基
板の製造へ応用せんとするものである。
研摩対象の結晶化ガラスは、材質が実質的に
(例えば20%以上)結晶化されたガラスで高強度、
高硬度を有し熱的、電気的に安定なものがよい。
このような条件を満たす結晶化ガラスは多数存
在する。析出結晶としては、β−ユークリプタイ
ト(Li2O・Al2O3・2SiO2)、β−スポジウメン
(Li2O・Al2O3・4SiO2)、石英(SiO2)、メタ硅酸
リチウム(Li2O・SiO2)、二硅酸リチウム
(Li2O・2SiO2)、或いはこれらの混合物を用いた
ものが最も一般的である。その他コージエライト
(2MgO・2Al2O3・5SiO2)、ガーナイト(ZnO・
Al2O3)、フツ素金雲母、アルカリケイ酸塩
(Na2O・Al2O3・2SiO2等)がある。
結晶化のために核生成剤を用いるのが一般的で
あるが核形成剤を用いないものもある。
核生成剤としては、感光性金属(Au、Ag、Cu
等)、貴金属(Pt、Pd等)、酸化チタン、酸化ジ
ルコニウム、フツ化物(CaF2等)、遷移金属化合
物(Cr、V、Fe、Co、Ni、Th、Mo等の酸化物
等)、燐酸化合物、ヒ素化合物(P2O5、As2O3
等)、Sb酸化物、Sn酸化物等を用いたものがあ
る。
結晶化ガラスの熱膨張係数は凡そ0〜130×
10-7/℃のものが得られるが、使用する磁性媒体
とのマツチングを考慮して選択することがかなり
広汎な範囲で可能であるという利点がある。例え
ばセンダストやパーマロイ等の軟磁性薄膜には熱
膨張係数の高いもの、セラミツク質の磁性媒体に
は対応して小さなもの、或いは温度変化に伴なう
デイスクのトラツク位置ズレを抑えるために低膨
張係数のものを選ぶ等の如く選択することが可能
である。
結晶化ガラスの好ましい例としては、SiO2−
Li2O(又はさらに−Al2O3)系のもの(さらにCe、
Ag等を含むもの)、Na2O系のもの等がある。結
晶粒度は微細なものがよく超精密研摩により無孔
化できる範囲に結晶化されたものを用いる。結晶
粒度80Å以下(さらに50Å以下)は好ましい。デ
イスクとしての使用のためには、強度は高い程よ
く、曲げ強度約1000Kg/cm2以上が好ましい。
純水中に懸濁させる無水アルミナ微粉末は、粒
径が320Å以下の略球状のものであり、乾式製法
により得られるが、その単位体積当りの表面積が
130m2/gを越える場合、粒形状が不規則形状と
なり、ラツプ時に研摩面に対する切削・引掻作用
が強く、得られる表面粗度が劣化し、研摩面に微
細突起、凹部が発生し易くなるので、単位体積当
りの表面積は130m2/g以下とする。
この発明に用いる無水アルミナ微粉末は乾式製
法により得られるため、湿式製法による含水アル
ミナに比べ、活性面積が100%と大きいため、反
応性に富み、加工効率を向上させるケミカル効果
が得られ、また、純度は99.9%以上となり微粉末
による表面への汚染が少なく研摩加工が安定す
る。水溶液はPH4〜5でシラノール基を呈し、ケ
ミカル効果が得られる。また、粉末形状が実質的
に球状であるため、研摩表面に対する切削、引掻
作用が少なく、研摩表面品位向上に有効である。
結晶化ガラスの主成分であるSiO2は負に帯電し
ており、微粉末自体は正に帯電するため、SiO2
と無水アルミナ粉末の懸濁液は電界効果により、
加工作用砥粒数が増加することになり、加工能率
の増大と共に凝集効果により、加工単位は数10Å
となり、結晶化ガラス表面を80Å好ましくは50Å
以下(さらには20Å以下のオーダーにまで)に精
密研摩することができると考えられる。
また、無水アルミナ微粉末の粒径が320Åを越
えると、被研摩表面に疵を形成し、表面粗度を劣
化させるので好ましくない。
研摩条件として、ラツプ荷重は、0.1Kg/cm2未
満では所要の表面粗度が得られず、かつ加工能率
が低く、また、2.0Kg/cm2を越えると加工効率の
点では好ましいが、ラツプ装置の大規模化に伴な
うコスト高と、研摩精度が悪化するので好ましく
ない。
また、ラツプ盤としては、Sn、Pb、はんだ合
金等の軟質金属あるいはクロス等が最適である。
ラツプ盤と被研摩材とは好ましくは相対回転して
研摩する。ここに用いる「純水」とは、有機物の
汚れを含有しないものでゴミ等(通例3000Å以上
のサイズを有する)を含まない水を称し、イオン
交換水、蒸留水等でよい。
[好適な実施の態様]
以下に、実施例を説明する。
被研摩結晶化ガラスには、ガラス質基地中に約
30%の結晶が晶出したフオトセラム(商品名、コ
ーニング社製造)を使用し、その試料は直径90mm
×2mm厚さで、被研摩面粗度300Åであつた。
研摩液は、単位体積当り表面積90m2/g〜120
m2/g、粒径300Åの非晶質無水アルミナ微粉末
を、純水中に1wt%分散させたPH4の懸濁液を使
用した。
加工機は両面ポリツシユ盤を用い、ポリツシヤ
ーには、600mmφのSn盤を用い、このポリツシヤ
ー表面にフオトセラムの被研削面を当接させ、回
転数60rpm、ラツプ荷重各0.5Kg/cm2、2Kg/cm2
の荷重負荷の加工条件で、両者を相対的に回転さ
せ、研摩加工中、100c.c./hの割合で研摩液を連
続滴下しながら、30分間研摩を実施した。
また、比較のため、砥粒にCeO2を使用した研
摩液の場合(比較例C)、含水アルミナ微粉末を
使用した研摩液の場合(比較例D)及び本発明と
同一の無水アルミナ微粉末を使用した研摩液を用
いて本発明条件外のラツプ荷重の場合(比較例
E)の各種加工条件で研摩した。この際の研摩条
件並びに被研摩材料の表面粗度を測定し、本発明
方法で得られた表面粗度測定結果と共に、第1表
に示す。
被研摩面の表面粗度は、表面段差測定器
(Talystep装置、スタイラス、0.5μm、針圧7mg)
を使用して測定し、表面部の突起及び凹部状態は
ノマルスキー微分干渉顕微鏡を使用して測定し
た。
第1表から明らかな如く、従来のガラス研摩方
法による比較例Cの場合は、結晶化ガラスに対し
ては300Åの表面粗度しか得られず、また、含水
アルミナ微粉末を使用した場合は、粒形状が不規
則で球状でなく、表面積が大きく、切削や引掻き
作用が大で表面粗度が劣化しており、さらに、本
発明方法の研摩液を使用しても、ラツプ荷重が条
件外であると、表面粗度は200Åしか得られず、
いずれの場合も、結晶化ガラスの精密研摩には不
適であるのに対し、本発明方法の場合は、結晶化
ガラス表面には突起や凹部の発生がなく、20Åの
すぐれた表面粗度が得られたことが分る。
ちなみに、本発明Aと比較例Cの各々の被研摩
面表面粗度を測定し、第1図、第2図の2種のス
ケールでグラフに表示する。第1図に示す本発明
による被研摩面は、第2図の従来方法による被研
摩面に対して著しく精密平坦面を得られることが
明白である。
[Technical Field] The present invention relates to a method of manufacturing a substrate for a magnetic disk by precision polishing the surface of a crystallized glass substrate for a magnetic disk. [Technical Background] Generally, the following characteristics are required for a magnetic disk substrate. (1) The surface roughness after polishing must be good to ensure stable flying of the magnetic head and stability of recording characteristics due to the low head flying height of 0.3 μm or less. (2) There are no protrusions or hole-like depressions that can cause defects in the magnetic thin film formed on the substrate surface. (3) Must have sufficient mechanical strength to withstand machining, polishing, or high-speed rotation during use. (4) It must have corrosion resistance, weather resistance, and heat resistance. Conventionally, Al alloys have been used for magnetic disk substrates, but Al alloy substrates suffer from the crystal anisotropy of the material,
Due to material defects and nonmetallic inclusions present in the material, during machining and polishing processes, these may remain as protrusions on the substrate surface, or crystallized portions may fall off in spots and cause depressions. Even after thorough polishing, the surface roughness is only about 200 Å at most, and the surface has protrusions, depressions, and undulations, making it unsatisfactory as a substrate material for high-density magnetic recording disks. Currently, in order to improve the surface condition of substrate materials for sputter disks, a method is being used to form an alumite layer on the surface of an Al alloy to increase hardness and improve polishability.
Since trace impurities (Fe, Mn, Si) in the Al alloy precipitate as intermetallic compounds, these areas become a cause of dent defects after alumite treatment. Increasing the purity of the base alloy is nearly impossible in terms of manufacturing process, and in the case of Al alloys, handling has also become a problem in terms of corrosion resistance and cleanliness. In addition, when forming a thin film magnetic recording medium by sputtering or plating, there are problems with chemical reaction and diffusion between the Al alloy and the magnetic film, and it is also necessary to heat-treat the magnetic film during the process. It is difficult to perform heat treatment because the shape accuracy deteriorates and the surface runout acceleration increases. There is also a method of forming oxides such as SiO 2 and Al 2 O 3 on an Al substrate by sputtering, but
The drawback is that the adhesion to the substrate after spatter formation is weak. In general, the quality of the processing of the magnetic disk substrate is determined by the runout of the magnetic disk, the acceleration component,
It depends on the signal error of the magnetic recording medium, etc. By the way, since Al alloy is a metal material, its Vickers hardness is around 100 (over 600 for ceramics).
The bending strength is also 1000Kg/ cm2 (4000Kg/cm2 for ceramics)
Kg/cm 2 or more), and as the recording density becomes higher, the shape accuracy such as slugs, scratches, flatness, and waviness becomes stricter, making processing even more difficult. During abrasive processing, abrasive grains tend to become packed together, resulting in defects. In addition, in the case of Al alloy substrates, sufficient consideration must be given to the manufacturing process, such as surface corrosion resistance, weather resistance, prevention of contamination, cleanliness, rust prevention, and dirt during the turning process, polishing process, and storage. . [Objective] The basic object of the present invention is to provide a novel method for manufacturing a magnetic disk substrate that eliminates the above-mentioned drawbacks and problems, and in particular, it is a basic object of the present invention to provide a method for manufacturing a new magnetic disk substrate that eliminates the above-mentioned drawbacks and problems. An object of the present invention is to effectively use dried crystallized glass as a substrate material for magnetic disks. [Summary of the structure of the invention] The present invention provides a magnetic disk substrate which is precision polished to a surface roughness of 80 Å or less in order to improve the characteristics and ensure reliability of the magnetized film formed on the surface of the crystallized glass substrate. Characterized by manufacturing method. That is, the method for manufacturing a magnetic disk substrate of the present invention involves suspending anhydrous alumina fine powder having a surface area per unit volume of 130 m 2 /g or less, a substantially spherical shape, and a particle size of 320 Å or less in pure water. The polishing liquid is used as a polishing liquid, and the crystallized glass to be polished and a lapping plate are placed opposite each other in the polishing liquid, and precision polishing is carried out while applying a lapping load of 0.1 to 2 kg/cm 2 . [Disclosure of the Invention] In the case of a crystallized glass substrate, the mechanical strength is stronger than that of an Al alloy, and it is relatively easy to control the shape accuracy in abrasive processing. Further, there is no need to pay special attention to corrosion resistance and weather resistance, and the surface can be cleaned by sputter cleaning when forming an insulating thin film by sputtering. Furthermore, when Al alloy is turned, a machining-altered layer remains on the surface, whereas in the case of crystallized glass, due to the mechanochemical polishing finish, the surface is no different from the stress strain in the bulk, and There is no strain transfer to the coated media. Nowadays, crystallized glass has come to be used for a wide range of applications in various fields due to its superior heat resistance, abrasion resistance, weather resistance, insulation properties, and mechanical strength compared to Al alloy substrates. In magnetic disk substrates whose surfaces are subjected to thin film media processing, as the density of media increases, there is an increasing need for smooth substrate surfaces and distortion-free substrates. When using crystallized glass as a magnetic disk substrate, there are problems such as dropouts due to surface micro defects and head crushing, which impair reliability. There were some difficulties. Conventionally, as a precision polishing method for crystallized glass, a fused amorphous glass polishing method, which is applied to photomasks, lenses, etc., has been adopted. This polishing method uses cerium oxide or red iron abrasive grains and can finish the surface of lenses, etc. to a roughness of 50 Å or less. However, even when applied to crystallized glass, since the material is substantially crystallized, fine protrusions and depressions are generated on the polished surface, resulting in a problem that only a surface roughness of about 250 Å can be obtained. For this purpose, the present inventors developed a method for high-precision surface polishing of crystallized glass and filed a patent application (Japanese Patent Application No. 155176-155178). That is, these relate to a polishing method for precisely polishing the surface of a crystallized glass substrate for a thin film magnetic head to a surface roughness of 50 Å or less. The present invention further seeks to apply the method to the manufacture of substrates for magnetic disks. The crystallized glass to be polished is glass whose material is substantially (for example, 20% or more) crystallized and has high strength.
It is preferable to use one that has high hardness and is thermally and electrically stable. There are many crystallized glasses that meet these conditions. Precipitated crystals include β-eucryptite (Li 2 O・Al 2 O 3・2SiO 2 ), β-spodiumene (Li 2 O・Al 2 O 3・4SiO 2 ), quartz (SiO 2 ), and metasilicic acid. The most common are those using lithium (Li 2 O.SiO 2 ), lithium disilicate (Li 2 O.2SiO 2 ), or a mixture thereof. Other cordierite (2MgO・2Al 2 O 3・5SiO 2 ), gahnite (ZnO・
Al 2 O 3 ), fluorine phlogopite, and alkali silicates (Na 2 O, Al 2 O 3 , 2SiO 2, etc.). Although it is common to use a nucleating agent for crystallization, there are some methods that do not use a nucleating agent. As a nucleating agent, photosensitive metals (Au, Ag, Cu
), noble metals (Pt, Pd, etc.), titanium oxide, zirconium oxide, fluorides (CaF 2, etc.), transition metal compounds (oxides of Cr, V, Fe, Co, Ni, Th, Mo, etc.), phosphoric acid compounds, arsenic compounds (P 2 O 5 , As 2 O 3
etc.), Sb oxide, Sn oxide, etc. The thermal expansion coefficient of crystallized glass is approximately 0 to 130×
10 -7 /°C, but it has the advantage that it can be selected from a wide range in consideration of matching with the magnetic medium used. For example, a soft magnetic thin film such as sendust or permalloy has a high thermal expansion coefficient, a ceramic magnetic medium has a correspondingly small one, or a low expansion coefficient to suppress disk track position shift due to temperature changes. It is possible to make a selection such as selecting one of the following. A preferable example of crystallized glass is SiO 2 −
Li 2 O (or even −Al 2 O 3 ) based (and Ce,
(containing Ag, etc.), Na 2 O-based products, etc. The crystal grain size is preferably fine and crystallized to a range that can be made non-porous by ultra-precision polishing. A crystal grain size of 80 Å or less (even 50 Å or less) is preferable. For use as a disk, the higher the strength, the better, and a bending strength of about 1000 Kg/cm 2 or more is preferred. The anhydrous alumina fine powder suspended in pure water is approximately spherical with a particle size of 320 Å or less, and is obtained by a dry manufacturing method, but the surface area per unit volume is
If it exceeds 130 m 2 /g, the grain shape becomes irregular, the cutting and scratching action on the polished surface is strong during lapping, the resulting surface roughness deteriorates, and micro protrusions and depressions are likely to occur on the polished surface. Therefore, the surface area per unit volume should be 130 m 2 /g or less. Since the anhydrous alumina fine powder used in this invention is obtained by a dry manufacturing method, it has a large active area of 100% compared to hydrated alumina produced by a wet manufacturing method, so it is highly reactive and has a chemical effect that improves processing efficiency. The purity is 99.9% or higher, which means less contamination of the surface by fine powder and stable polishing. The aqueous solution exhibits silanol groups at pH 4 to 5, and a chemical effect can be obtained. Furthermore, since the powder shape is substantially spherical, there is little cutting or scratching effect on the polished surface, which is effective in improving the polished surface quality.
SiO 2 , the main component of crystallized glass, is negatively charged, and the fine powder itself is positively charged, so SiO 2
and anhydrous alumina powder suspension due to electric field effect,
The number of abrasive grains for processing increases, and the processing efficiency increases and the agglomeration effect reduces the processing unit to several tens of Å.
Therefore, the crystallized glass surface should be 80 Å, preferably 50 Å
It is thought that precision polishing can be performed to the following (even to the order of 20 Å or less). Furthermore, if the particle size of the anhydrous alumina fine powder exceeds 320 Å, it is not preferable because it will form scratches on the surface to be polished and deteriorate the surface roughness. As for the polishing conditions, if the lap load is less than 0.1 kg/cm 2 , the required surface roughness cannot be obtained and the machining efficiency is low; if it exceeds 2.0 kg/cm 2 , it is preferable in terms of machining efficiency, but the lap load is This is not preferable because it increases the cost as the scale of the device increases and the polishing accuracy deteriorates. In addition, soft metals such as Sn, Pb, solder alloys, cloth, etc. are most suitable for the lap board.
The lapping machine and the material to be polished are preferably polished in relative rotation. "Pure water" as used herein refers to water that does not contain organic dirt and dust (usually having a size of 3000 Å or more), and may be ion-exchanged water, distilled water, or the like. [Preferred embodiments] Examples will be described below. The crystallized glass to be polished has approximately
Photoceram (trade name, manufactured by Corning Inc.) with 30% crystallization was used, and the sample was 90 mm in diameter.
It was 2 mm thick and had a surface roughness of 300 Å. The polishing liquid has a surface area of 90 m 2 /g to 120 m 2 /g per unit volume.
A PH4 suspension in which 1 wt % of amorphous anhydrous alumina fine powder having a particle diameter of 300 Å and m 2 /g was dispersed in pure water was used. The processing machine uses a double-sided polisher, and the polisher uses a 600mmφ Sn disk, and the polished surface of the photoceram is brought into contact with the surface of the polisher.The rotation speed is 60rpm, and the lap loads are 0.5Kg/cm 2 and 2Kg/cm, respectively. 2
Polishing was carried out for 30 minutes under the processing conditions of a load loading of 100 cm, while rotating the two relative to each other, and continuously dropping the polishing liquid at a rate of 100 c.c./h during the polishing process. In addition, for comparison, a case of a polishing liquid using CeO 2 as the abrasive grains (Comparative Example C), a case of a polishing liquid using a hydrated alumina fine powder (Comparative Example D), and an anhydrous alumina fine powder same as the present invention are also shown. Polishing was carried out under various processing conditions using a polishing liquid using a polishing solution using a lap load other than the conditions of the present invention (Comparative Example E). The polishing conditions at this time and the surface roughness of the material to be polished were measured, and are shown in Table 1 together with the surface roughness measurement results obtained by the method of the present invention. The surface roughness of the polished surface was measured using a surface step measuring device (Talystep device, stylus, 0.5 μm, stylus force 7 mg).
The state of protrusions and recesses on the surface was measured using a Nomarski differential interference microscope. As is clear from Table 1, in the case of Comparative Example C using the conventional glass polishing method, a surface roughness of only 300 Å was obtained for crystallized glass, and when using hydrated alumina fine powder, The grain shape is irregular and not spherical, the surface area is large, the cutting and scratching action is large, and the surface roughness is deteriorated.Furthermore, even if the polishing liquid of the present invention is used, the lap load is outside the conditions. If there is, a surface roughness of only 200 Å can be obtained,
In either case, it is unsuitable for precision polishing of crystallized glass, whereas in the case of the method of the present invention, there are no protrusions or depressions on the surface of crystallized glass, and an excellent surface roughness of 20 Å is obtained. I can see that it was done. Incidentally, the surface roughness of each polished surface of Invention A and Comparative Example C was measured and graphed on two scales shown in FIG. 1 and FIG. 2. It is clear that the surface to be polished according to the present invention shown in FIG. 1 provides a much more precisely flat surface than the surface to be polished according to the conventional method shown in FIG.
【表】
また、本発明において、結晶化ガラスを用いた
磁気デイスク基板の表面粗度は、80Å以下である
と同時に表面欠陥もなく、半径方向の真直性は
0.5μm、平面度1.5μm、端面ダレはなくAl合金旋
削加工した基板に比べ磁気デイスクの形状精度も
優れている。
すなわち、本発明は磁気デイスク基板に結晶化
ガラスを用いたこと、及び結晶化ガラスの精密研
摩方法により、磁気デイスクの信頼性、電磁変換
特性及び歩留の向上に極めて有効なことが分る。[Table] In addition, in the present invention, the surface roughness of the magnetic disk substrate using crystallized glass is 80 Å or less, there are no surface defects, and the straightness in the radial direction is
0.5 μm, flatness 1.5 μm, no edge sag, and the shape accuracy of the magnetic disk is superior to that of a substrate made of aluminum alloy turned. That is, it can be seen that the present invention is extremely effective in improving the reliability, electromagnetic conversion characteristics, and yield of magnetic disks by using crystallized glass for the magnetic disk substrate and by using the precision polishing method for crystallized glass.
第1図、第2図は、夫々本発明の実施例、比較
例の被研摩面表面粗度の測定結果を各a,b異つ
たスケールで示すグラフである。
FIGS. 1 and 2 are graphs showing the measurement results of the surface roughness of the surfaces to be polished of an example of the present invention and a comparative example, respectively, on different scales a and b.
Claims (1)
状が実質的に球状の粒径320Å以下の無水アルミ
ナ微粉末を純水中に懸濁させた液を研摩液とし該
研摩液を用い、被研摩結晶化ガラスとラツプ定盤
を対向させて、ラツプ荷重0.1〜2Kg/cm2を加え
ながら精密研摩して成る表面粗度80Å以下且つ無
歪の表面層を形成することを特徴とする磁気デイ
スク用基板の製造方法。1. A polishing solution prepared by suspending anhydrous alumina fine powder with a surface area of 130 m 2 /g or less, a substantially spherical shape, and a particle size of 320 Å or less in pure water is used as a polishing solution. A magnetic disk characterized by forming a surface layer with a surface roughness of 80 Å or less and no strain, which is formed by precision polishing a polished crystallized glass and a lap surface plate facing each other while applying a lap load of 0.1 to 2 kg/cm 2. method for manufacturing substrates for
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8565684A JPS60229234A (en) | 1984-04-27 | 1984-04-27 | Substrate for magnetic disk and its production |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8565684A JPS60229234A (en) | 1984-04-27 | 1984-04-27 | Substrate for magnetic disk and its production |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60229234A JPS60229234A (en) | 1985-11-14 |
| JPH044656B2 true JPH044656B2 (en) | 1992-01-29 |
Family
ID=13864863
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8565684A Granted JPS60229234A (en) | 1984-04-27 | 1984-04-27 | Substrate for magnetic disk and its production |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60229234A (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62120629A (en) * | 1985-11-20 | 1987-06-01 | Sumitomo Special Metals Co Ltd | Magnetic disk and its production |
| JP2737901B2 (en) * | 1987-09-09 | 1998-04-08 | 旭硝子株式会社 | Method for manufacturing glass substrate for magnetic disk |
| JPH06290451A (en) * | 1992-05-13 | 1994-10-18 | Matsushita Electric Ind Co Ltd | Substrate for magnetic disk and its production |
| JP2516553B2 (en) * | 1993-05-19 | 1996-07-24 | 株式会社オハラ | Crystallized glass for magnetic disk and manufacturing method thereof |
| EP0729924B1 (en) * | 1993-05-19 | 2000-01-26 | Kabushiki Kaisha Ohara | Glass-ceramic for a magnetic disk substrate |
| JP3219705B2 (en) * | 1996-11-14 | 2001-10-15 | 株式会社オハラ | Glass ceramic substrate for magnetic information storage media |
| US6383404B1 (en) | 1998-08-19 | 2002-05-07 | Hoya Corporation | Glass substrate for magnetic recording medium, magnetic recording medium, and method of manufacturing the same |
| US7606721B1 (en) | 2003-01-31 | 2009-10-20 | CDR Associates, LLC | Patient credit balance account analysis, overpayment reporting and recovery tools |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS49122306A (en) * | 1973-03-24 | 1974-11-22 |
-
1984
- 1984-04-27 JP JP8565684A patent/JPS60229234A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60229234A (en) | 1985-11-14 |
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