JPH0373411A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPH0373411A JPH0373411A JP13616790A JP13616790A JPH0373411A JP H0373411 A JPH0373411 A JP H0373411A JP 13616790 A JP13616790 A JP 13616790A JP 13616790 A JP13616790 A JP 13616790A JP H0373411 A JPH0373411 A JP H0373411A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- magnetic
- oxygen
- film
- magnetic 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.)
- Granted
Links
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000001301 oxygen Substances 0.000 claims abstract description 15
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 15
- 239000000758 substrate Substances 0.000 claims description 8
- 239000010410 layer Substances 0.000 abstract 13
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 abstract 2
- 239000002344 surface layer Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 18
- 239000010409 thin film Substances 0.000 description 8
- 238000004458 analytical method Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000000151 deposition Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229910000599 Cr alloy Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000696 magnetic material Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 241000283690 Bos taurus Species 0.000 description 1
- 229910000684 Cobalt-chrome Inorganic materials 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 206010061926 Purulence Diseases 0.000 description 1
- 239000010952 cobalt-chrome Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 229910001004 magnetic alloy Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000010702 perfluoropolyether Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000000682 scanning probe acoustic microscopy Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Magnetic Record Carriers (AREA)
- Manufacturing Of Magnetic Record Carriers (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は磁気記録媒体に関する。更に詳細には、本発明
はCo−Crからなる記録磁性層の機械特性が改溌され
た磁気記録媒体に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to magnetic recording media. More specifically, the present invention relates to a magnetic recording medium in which the mechanical properties of a recording magnetic layer made of Co--Cr are improved.
[従来の技術]
非磁性基体上にCo−Cr等の金属磁性膜をイfする薄
膜型磁気記録媒体は高密度記録用媒体として注目され、
実用化に向けて研究開発が行われている。特に、Co−
Crは神めて耐食性に優れた磁性合金であり、そのメリ
ットを活かすべく、!に直磁気記録や面内記録などの薄
膜型磁気記録媒体材料として幅広く検A’tが行われて
いる。[Prior Art] Thin-film magnetic recording media, in which a metal magnetic film such as Co-Cr is deposited on a non-magnetic substrate, are attracting attention as high-density recording media.
Research and development is underway toward practical application. In particular, Co-
Cr is a magnetic alloy with excellent corrosion resistance, and in order to take advantage of its merits,! In recent years, a wide range of tests have been carried out as materials for thin-film magnetic recording media such as direct magnetic recording and in-plane recording.
[発明が解決しようとする課題]
しかし、現段階においてCo−Cr合金からなる薄膜型
磁気記録媒体の機械的耐久v1:、は満足できるもので
なく、このことにより丈用化が遅れている。[Problems to be Solved by the Invention] However, at the present stage, the mechanical durability v1: of thin film magnetic recording media made of Co--Cr alloys is not satisfactory, and as a result, the increase in the length of use has been delayed.
薄膜型磁気j己録媒体の機械的耐久性の決定要因は7二
つある。一つは、磁気ヘッドの摺動により表面の潤滑剤
が枯渇し、記録磁性層がIg托して寿命に至るというパ
ターンである。もう一つは、磁気ヘッド加工技術の限界
から生じる摺動面における光種材質間の段差およびスラ
イダ一端部の鋭いエツジなどが薄膜媒体表面に接触し、
損傷が生じて瞬時に寿命に至るというパターンである。There are seven factors that determine the mechanical durability of thin-film magnetic self-recording media. One pattern is that the lubricant on the surface is depleted due to the sliding of the magnetic head, and the recording magnetic layer absorbs Ig, reaching the end of its life. The other problem is that the difference in level between the optical seed materials on the sliding surface and the sharp edge at one end of the slider, which arise from the limitations of magnetic head processing technology, come into contact with the surface of the thin film medium.
This is a pattern in which damage occurs and the service life ends instantly.
人体において、薄膜型磁気記録媒体の場合には後者のパ
ターン、すなわち、記録磁性層が序耗により寿命に〒る
遥以前に、上記のような局所的外力により損傷を牛じ、
寿命に至るというのが一般的であった。In the human body, in the case of thin-film magnetic recording media, the latter pattern occurs, i.e., long before the recording magnetic layer reaches the end of its lifespan due to wear and tear, damage can occur due to the above-mentioned local external force.
It was common to reach the end of one's lifespan.
こうした大きな局所的外力に耐えうるようにするために
、記録磁性JIllltに種々の硬質保j1!膜を設け
ることが検討されてきた。しかし、機械強度的にはいず
れも満足できるものではなく、記録媒体の一4久PIを
充分に向りすることができなかった。In order to withstand such large local external forces, various hard materials are applied to the recording magnetic field. Providing a membrane has been considered. However, none of them were satisfactory in terms of mechanical strength, and could not be sufficiently applied to the 14-year PI of the recording medium.
本発明はかかる従来技術がもつ欠点を解消し、以て耐久
性に優れた磁気記録媒体を提供することを1−1的とす
る。An object of the present invention is to eliminate the drawbacks of the prior art and thereby provide a magnetic recording medium with excellent durability.
[課題を解決するための手段コ
+1il記l」的を達成するための手段として、本発明
では、CoCr磁性崩表面から深さ20nmの範聞内に
酸素含汀墳及びCr存花比Cr/(C。[Means for Solving the Problems] In the present invention, an oxygen-containing mound and a Cr-containing tomb within a depth of 20 nm from the CoCr magnetic collapse surface and Cr/ (C.
+Cr)のピークを7f、在させ、かつ1】9者を後者
よりも膜表面側に#?’Eせしめることにより、上記C
o−Cr&11性層の耐久性を高めるようにしている。+Cr) peak at 7f, and 1]9 is located closer to the membrane surface than the latter. 'E By forcing the above C
The durability of the o-Cr&11 layer is increased.
[作用コ
このような膜厚深さ方向の組成分布を設けることにより
耐久性が向りする原因としては、以ドのメカニズムが考
えられる。[Function] The following mechanism is considered to be the reason why the durability is improved by providing such a composition distribution in the depth direction of the film thickness.
すなわち、膜表面近傍に於いては比較的にC。In other words, C is relatively high near the film surface.
リッチの組成であり、なおかつ酸素が多hlに混入して
いる。そのためCoは部分的に酸素と結合l7、CoO
なとの優れた低摩擦層をその表面に形成している。、更
にその深部にCrリッチの部分があると、そのCrは一
部酸素と結合し、Cr 203をEとする硬質層を形成
する。It has a rich composition and contains a large amount of oxygen. Therefore, Co partially combines with oxygen l7, CoO
An excellent low-friction layer is formed on its surface. Furthermore, if there is a Cr-rich part deep inside, some of the Cr combines with oxygen to form a hard layer with Cr 203 as E.
このように本発明におけるCo−Cr薄膜は、第1図に
示されるように、co−Cr磁性月1のにに硬質層3、
史に低摩擦層5といった擬似ニー。膚に近い状態になっ
ているものと推測される。符号7は非磁性基体を示す。As shown in FIG. 1, the Co--Cr thin film in the present invention has a co--Cr magnetic layer 1, a hard layer 3,
A pseudo-knee with a low friction layer 5. It is assumed that the condition is close to that of the skin. Reference numeral 7 indicates a nonmagnetic substrate.
なお、これらの組成変調部は膜最面から深さ20nmの
範囲にあることが奸ましく120nrnを越えても耐久
性の杆しい改誇は見られず、むしろ磁気ヘッド−媒体間
の距離の増加による記録i11牛特性の劣化を生じせし
める。It should be noted that these compositionally modulated parts are in a range of 20 nm deep from the top surface of the film, and even if the depth exceeds 120 nrn, no significant improvement in durability is observed, rather the distance between the magnetic head and the medium increases. Recorded i11 due to increased deterioration of cattle characteristics.
また、Co−Cr磁姓層表層に形成されるC「(j 4
’、比のビーク偵は、0.3以−Lであることが好まし
い。これは、Cr??在比が0.3未満になると、上記
硬質部の形成が不充分となり、磁気ヘッドの摺動に対し
極めて傷つきやすくなるためと考えられる。In addition, C'(j 4
It is preferable that the peak ratio is 0.3 or more -L. Is this Cr? ? This is believed to be because when the retention ratio is less than 0.3, the hard portion is insufficiently formed and becomes extremely susceptible to damage by sliding of the magnetic head.
本発明の磁気記録媒体の製造方法は特に限定されないが
、−例として、酸素プラズマ中で表面処fil!するこ
とにより製造できる。Although the method for manufacturing the magnetic recording medium of the present invention is not particularly limited, for example, surface treatment fil! It can be manufactured by
別法として、磁性周表面をN!素雰囲気中で加熱処即す
ることによっても製造できる。Alternatively, the magnetic circumferential surface can be N! It can also be produced by heat treatment in an elementary atmosphere.
本発明の磁気記録媒体では、Co−Cr磁性荊を非磁性
基体上に形成させる際、ド地層を介在させることもでき
るが、本発明の必須要件ではない。In the magnetic recording medium of the present invention, when a Co--Cr magnetic layer is formed on a non-magnetic substrate, a magnetic layer may be interposed, but this is not an essential requirement of the present invention.
ド地層は例えばs T iなとの非磁性材料を基板上に
蒸着させることにより容易に形成させることができる。The magnetic layer can be easily formed by depositing a non-magnetic material such as s Ti on the substrate.
本発明の磁性層の最外層表面には市川の保護屑および/
または潤滑層を設けることもできる。The surface of the outermost layer of the magnetic layer of the present invention is coated with Ichikawa's protective dust and/or
Alternatively, a lubricating layer can also be provided.
[実施例] 以下、実施例により本発明を更に詳細に説明する。[Example] Hereinafter, the present invention will be explained in more detail with reference to Examples.
失丑艷1に
4枚の直径5.25インチの耐熱ガラス基板上に厚さ0
.23μmのCotaCrzz層を高周波スパッタリン
グ法により作製した。スパッタ条件としては、A rJ
IE5mTorr 、 g堆積速度10A/seeであ
った。以上のようにして作製した4枚の試料を)A板温
度100℃の状態で、圧力10〜2QTorrのNt毒
素プラズマ中O〜10分間曝した。0 thickness on 4 heat-resistant glass substrates with a diameter of 5.25 inches
.. A 23 μm CotaCrzz layer was fabricated by high frequency sputtering. The sputtering conditions are A rJ
The IE was 5 mTorr, and the g deposition rate was 10 A/see. The four samples prepared as described above were exposed to Nt toxin plasma at a pressure of 10 to 2 Q Torr for 0 to 10 minutes at a plate A temperature of 100°C.
暴露時ranの相違により、拭材A、B、Cおよび1〕
と分類する。試料Aの酸素プラズマ暴露時間は0分間、
Bは2分間、Cは7分間そして1)は0.6分間であっ
た。その後、各試料表面に膿度0.1vt%のフッ素糸
潤滑剤フォンプリン(モンテディソン社製)を準布した
上で耐久性を3・r価した。耐久性の評価は球面FP1
動拭験により行い、摺動子の押しつけ荷重20g、相対
速度2m/seeの条件でGo−Cr記録層に傷が発生
する摺動回数を1記録媒体の耐摺動強度と定義した。ま
た上記Go−Cr層の深さ方向組成分析は、以下の条件
でオージェ電子分光分析法(以ド、オージェ分析と呼ぶ
ことにする)により求めた。その結果を第2閏に雁す。Wiping materials A, B, C and 1] due to the difference in ran during exposure.
Classify as. The oxygen plasma exposure time of sample A was 0 minutes;
B was 2 minutes, C was 7 minutes, and 1) was 0.6 minutes. Thereafter, a fluorine thread lubricant Fonpurin (manufactured by Montedison) with a purulence of 0.1 vt% was applied to the surface of each sample, and the durability was evaluated with a 3.r value. Durability evaluation is spherical FP1
The sliding strength of one recording medium was defined as the number of times the Go-Cr recording layer was slid under the conditions of a sliding force of 20 g and a relative speed of 2 m/see, through a dynamic wiping test. Further, the depth direction composition analysis of the Go-Cr layer was determined by Auger electron spectroscopy (hereinafter referred to as Auger analysis) under the following conditions. Transfer the result to the second leap.
第2図において、横軸はエツチング深さ、縦軸は酸素の
ピーク強度及びCrJftE比(Cr/(Co+Cr)
)をとった。なおオージェ分析を行う際には、分析試料
表面の吸着ガスを取り除くために、10秒間Arエツチ
ング処理を行った。In Fig. 2, the horizontal axis is the etching depth, and the vertical axis is the oxygen peak intensity and the CrJftE ratio (Cr/(Co+Cr)).
) was taken. Note that when performing Auger analysis, Ar etching treatment was performed for 10 seconds in order to remove adsorbed gas on the surface of the analysis sample.
また、表1にこれらの試料の耐摺動強度測定結果を小す
〇
左上
第2図および表1に示された結果から明らかなように、
膜表面から、酸素含打量ビーク、Cr h在住ピークの
順で存在し、かつCr7F在比のピーク値が0.3以り
であるCo−Cr膜が優れた耐久性を承すことがわかる
。In addition, Table 1 shows the results of measuring the sliding strength of these samples. As is clear from the results shown in Figure 2, upper left, and Table 1,
It can be seen that a Co--Cr film in which an oxygen content peak and a Cr h resident peak exist in this order from the film surface, and in which the peak value of the Cr7F content ratio is 0.3 or more has excellent durability.
L胤梢1
jlさ30μmのポリイミドフィルム(宇部興産社製、
ユービレックス・Sタイプ)を)X板とし、第3図に/
i<シた連続券取式11′乍夙着装置により、Jk根板
上Co−Cr合金膜を形成した。この薄膜の形成P順を
以ドに説明する。先ず、rc’+槽内を5×10−θT
orr以ドにまでυ1気した後、キャン12を220℃
に加熱した。そして、供給ロール10からベースフィル
ムノλ板14を送り出し、膜形成後、巻取ロール13に
よりベースフィルム)λ板を巻き取った。この時の膜堆
積速度は3000Å/seeであり、得られた膜厚は2
000Åで、膜組成はCo−18at%Crであった。L seedling 1 Polyimide film with a thickness of 30 μm (manufactured by Ube Industries, Ltd.)
Ubilex S type) is used as )X plate, and in Figure 3 /
A Co--Cr alloy film was formed on the Jk base plate using a continuous ticket-taking type 11' paper bonding device. The order of formation P of this thin film will be explained below. First, the temperature inside the rc'+ tank is 5×10-θT.
After increasing the temperature to υ1 below orr, set the can 12 to 220℃.
heated to. Then, the base film λ plate 14 was sent out from the supply roll 10, and after film formation, the base film λ plate was wound up by the take-up roll 13. The film deposition rate at this time was 3000 Å/see, and the obtained film thickness was 2
000 Å, and the film composition was Co-18at%Cr.
このようにして形成した蒸着膜より、l 5cmX 3
0cmのサイズに試料を切り出し、人気中で所定温度に
加熱したホットプレートヒに試料を押しZて、酸化を行
った。酸化温度および時[ijJはそれぞれ、400℃
およびO〜80secの範囲内で変化させた。このよう
にして処理した膜の耐久性を球面摺動拭験により評価し
た。摺動rとしては曲率5 mmのMn−Zn多粘品フ
ェライト摺動rを用い、これを試料表面に20gの荷改
で押し付けた上で、平均相対速度2IIIII/IIn
で摺動させた。また、評価にあたってはCo−Cr膜表
面に潤滑剤として濃度0゜2wt%のパーフルオロポリ
エーテルを塗布した。From the vapor deposited film thus formed, 1 5 cm x 3
A sample was cut out to a size of 0 cm and oxidized by pressing it onto a hot plate heated to a predetermined temperature. Oxidation temperature and time [ijJ are each 400°C
and was varied within the range of 0 to 80 sec. The durability of the membrane thus treated was evaluated by a spherical sliding test. A Mn-Zn multi-viscous ferrite slider with a curvature of 5 mm was used as the slide r, and after pressing it onto the sample surface with a load change of 20 g, an average relative velocity of 2III/IIn was applied.
I slid it with. Further, in the evaluation, perfluoropolyether at a concentration of 0.2 wt% was applied as a lubricant to the surface of the Co--Cr film.
、i=F’ 41鮎果を第4図に示す。また、400℃
で4秒間酸化した試料のオージェ深さ方向分析結果を第
5図に示す。, i=F' 41Ayuka is shown in FIG. Also, 400℃
Fig. 5 shows the results of Auger depth direction analysis of a sample oxidized for 4 seconds.
第4図および第5図に示された結果から明らかなように
、400’C程度の比較的高温度で、短叫間酸化処理し
た場合にも、膜表面から、酸素31丁mビークおよびC
r存在比ピークの順で存在し、かつs Cr存7L比の
ピーク値が0.3以上である優れた耐久性を何するGo
−Cr膜が得られる。As is clear from the results shown in FIGS. 4 and 5, even when oxidation treatment is performed for a short period of time at a relatively high temperature of about 400'C, a 31 m peak of oxygen and a C
What is excellent durability that exists in the order of r abundance ratio peak and s Cr abundance ratio peak value of 0.3 or more?
-Cr film is obtained.
なお、−]二二酸化の際の処理温度は、基板材質および
磁性荊材料に依存す木が、概ね、上阻の温度は600℃
であり、この温度を越えるとCo−Cr磁性膜の磁気特
件が大きく変化するようになる。In addition, -] The treatment temperature during oxidation depends on the substrate material and magnetic material, but the upper temperature is generally 600°C.
When this temperature is exceeded, the magnetic characteristics of the Co--Cr magnetic film change significantly.
[発明の効果コ
以ト説明したように、本発明によれば、Co −Cr磁
性層の深さ20nmの範囲内に表面から酸素含fT F
Wt、Cr h在住のピークを順次存許せしめ、後者の
ピーク値を0.3以−Lとすることにより、その耐久性
を著しく数円できる。[Effects of the Invention] As explained below, according to the present invention, oxygen-containing fT
By sequentially allowing the peaks of Wt and Cr h to exist, and by setting the latter peak value to 0.3 or more -L, the durability can be significantly reduced by several yen.
第1図は本発明の磁気記録媒体の構造を示す概要断面図
であり、第2図(A)〜(I))は実施例で作製された
試料A−DのCo−Cr膜表面の深さ方向組成分析結果
を示す特外図であり、第3図は実施例2における磁気記
録媒体の作製に使用される連続巻取式LT、’!蒸着装
置の模式図であり、第4図は処胛時間に対する耐久性の
関係を示すグラフ図であり、第5図は400℃で4秒間
酸化した試料のオージェ深さ方向分析結果を示すグラフ
図である。
1・・・Co−Cr磁性層、3・・・硬質胴。
5・・・低摩擦層、7・・・非磁性双体。
lO・−・供給ロール、12・・・キャン。
i3・・・巻取ロール。
14・・・ベースフィルム基板。
15・・・防it板。
t6・・・Co−Cr合余充填ルツボ。
17・・・電子銃。
18・・・排気孔FIG. 1 is a schematic cross-sectional view showing the structure of the magnetic recording medium of the present invention, and FIG. FIG. 3 is a special diagram showing the results of longitudinal composition analysis, and FIG. 3 is a continuous winding type LT used for manufacturing the magnetic recording medium in Example 2. Fig. 4 is a schematic diagram of the vapor deposition apparatus, Fig. 4 is a graph showing the relationship between durability and processing time, and Fig. 5 is a graph showing the results of Auger depth direction analysis of a sample oxidized at 400°C for 4 seconds. It is. 1...Co-Cr magnetic layer, 3...Hard body. 5...Low friction layer, 7...Nonmagnetic twin body. lO--supply roll, 12...can. i3... Winding roll. 14...Base film substrate. 15... IT-proof board. t6... Co-Cr combination extra filling crucible. 17...Electron gun. 18...Exhaust hole
Claims (2)
Co−Cr磁性層を形成した磁気記録媒体において、C
o−Cr膜表面から深さ20nmの範囲内に、酸素含有
量及びCr存在比Cr/(Co+Cr)のピークがあり
、前者が後者よりも膜表面側にあることを特徴とする磁
気記録媒体。(1) In a magnetic recording medium in which a Co-Cr magnetic layer is formed on a non-magnetic substrate with or without an underlayer, C
A magnetic recording medium characterized in that there are peaks of oxygen content and Cr abundance ratio Cr/(Co+Cr) within a depth of 20 nm from the surface of the o-Cr film, and the former is located closer to the film surface than the latter.
徴とする請求項1記載の磁気記録媒体。(2) The magnetic recording medium according to claim 1, wherein the peak of the Cr abundance ratio is 0.3 or more.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13217689 | 1989-05-25 | ||
JP1-132176 | 1989-05-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0373411A true JPH0373411A (en) | 1991-03-28 |
JP2847567B2 JP2847567B2 (en) | 1999-01-20 |
Family
ID=15075155
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13616790A Expired - Lifetime JP2847567B2 (en) | 1989-05-25 | 1990-05-25 | Magnetic recording media |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2847567B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012165113A1 (en) | 2011-06-02 | 2012-12-06 | 株式会社マキタ | Power tool |
US8888642B2 (en) | 2011-03-31 | 2014-11-18 | Makita Corporation | Power tool |
US8911320B2 (en) | 2009-08-28 | 2014-12-16 | Makita Corporation | Power tool |
-
1990
- 1990-05-25 JP JP13616790A patent/JP2847567B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8911320B2 (en) | 2009-08-28 | 2014-12-16 | Makita Corporation | Power tool |
US8888642B2 (en) | 2011-03-31 | 2014-11-18 | Makita Corporation | Power tool |
WO2012165113A1 (en) | 2011-06-02 | 2012-12-06 | 株式会社マキタ | Power tool |
Also Published As
Publication number | Publication date |
---|---|
JP2847567B2 (en) | 1999-01-20 |
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