JPH0428660B2 - - Google Patents

Info

Publication number
JPH0428660B2
JPH0428660B2 JP9037086A JP9037086A JPH0428660B2 JP H0428660 B2 JPH0428660 B2 JP H0428660B2 JP 9037086 A JP9037086 A JP 9037086A JP 9037086 A JP9037086 A JP 9037086A JP H0428660 B2 JPH0428660 B2 JP H0428660B2
Authority
JP
Japan
Prior art keywords
glass
crystallized glass
heads
present
magnetic
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
Application number
JP9037086A
Other languages
Japanese (ja)
Other versions
JPS62246840A (en
Inventor
Masayuki Ninomya
Hiroki Yamazaki
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Electric Glass Co Ltd
Original Assignee
Nippon Electric Glass Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Electric Glass Co Ltd filed Critical Nippon Electric Glass Co Ltd
Priority to JP9037086A priority Critical patent/JPS62246840A/en
Publication of JPS62246840A publication Critical patent/JPS62246840A/en
Publication of JPH0428660B2 publication Critical patent/JPH0428660B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C10/00Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition
    • C03C10/0054Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition containing PbO, SnO2, B2O3

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Glass Compositions (AREA)
  • Magnetic Heads (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

産業上の利用分野 本発明は、電子部品材料に用いられる部材、特
にコンピユータの記録装置等に使用されるフロツ
ピーデイスクドライブ用ヘツドのフエライトやセ
ラミツクス等を加圧接着するのに適した磁気ヘツ
ド用結晶化ガラスに関するものである。 従来技術 一般にフロツピーデイスクドライブ用ヘツド
は、図面に示すようにフエライトからなる記録再
生ヘツド1及び消去ヘツド2とセラミツクスから
なる磁気分離帯としてのセンタースペーサ3、ヘ
ツドの摩耗を防止するスライダー4で構成されて
おり、ヘツド1,2は各々ギヤツプ部5及び補強
ガラス6を有している。従来よりヘツド1,2と
センタースペーサ3、スライダー4との接着には
有機接着剤が用いられていたが、温湿度の変化に
よりセンタースペーサ3やスライダー4と精密な
相対位置を保持しているヘツド1,2が移動し、
特性が劣化するという問題があるため、最近では
有機接着材に代つて封着用ガラスが用いられてい
る。しかしながら封着用ガラスは、接着界面に気
泡が混入しやすく、特にヘツド1,2の表面に気
泡が混在するとデイスクの磁性粉がそこに沈着し
てデイスクの磁気記録面を傷つけ、磁気特性を悪
くするという問題がある。 またスライダー4としてセラミツクス以外にも
結晶化ガラスが用いられているが、表面粗度が大
きいためヘツド1,2との接着性が悪いと共にヘ
ツド1,2やセンタースペーサ3と接着する場合
必ず接着剤が必要であつた。すなわち一般に結晶
化ガラスをスライダーして直接ヘツド1,2やセ
ンタースペーサ3と接着する場合、結晶化ガラス
の接着温度がギヤツプ部5の封着温度より高いと
接着時にギヤツプ部5の有機接着剤や封着用ガラ
スが軟化し、完成したヘツド1,2のギヤツプ長
やトラツク幅に変形が生じやすくなるが、従来の
結晶化ガラスの屈伏点は850℃以上であり、スラ
イダー4として用いた場合接着温度がギヤツプ部
5の封着温度より高くなりやすくなるからであ
る。 発明の目的 発明は、上記問題点に鑑みなされたもので、電
子部品材料に用いられる部材として、接着剤を用
いるこなく直接フエライトやセラミツクス等低温
加熱によつて強固に加圧接着するこができ、発泡
が少なく、機械的強度が高い磁気ヘツド用結晶化
ガラスを提供することを目的とするものである。 発明の構成 本発明の磁気ヘツド用結晶化ガラスは、重量%
で、SiO2 60〜85%、Li2O 7〜15%、K2O 1〜
7%、Na2O 0.1〜7%、K2O+Na2O 2〜14%、
P2O5 0.1〜5%、Al2O3 1〜10%、PbO 2.5〜10
%、B2O5 0〜7%の組成を含有し、且つ上記成
分の合計が95%以上であることを特徴とする。 本発明における磁気ヘツド用結晶化ガラスの組
成範囲上記のように定した理由は以下のおりであ
る。 SiO2が60%より少ない場合は、化学耐久性が
悪くなり、85%より多い場合は、ガラスの作業性
が悪くなる。 Li2Oが7%より少ない場合は、結晶化度が低
くなつて熱膨張係数が高くなりす、15%より多い
場合は、結晶化度が上がり屈伏点が高くなりすぎ
る。 K2OとNa2Oは結晶化ガラスの熱膨張係数高め
るのに効果があるが、各々単独で用いると結晶化
ガラス中のガラスマトリツクス相で結晶構成成分
でないアルカリ成分が多量含まれ、ガラスマトリ
ツクス相が不安定になるため、本発明においては
K2Oを1〜7%、Na2Oを0.1〜7%と両成分を共
存させることによる混合アルカリ効果によつてガ
ラスマトリツクス相を安定させ、屈伏点の低い結
晶化ガラスが得られる。 K2Oが1%より少ない場合は、屈伏点が高くな
りすぎ、7%より多い場合はガラスが結晶化しに
くくなる。 Na2Oが0.1%より少ない場合は、前記混合アル
カリ効果が発揮されず、屈伏点が高くなりすぎ、
7%より多い場合はガラスが結晶化しにくくな
る。 K2OとNa2Oの合量が2%より少ない場合は、
屈伏点が高くなりすぎ、14%より多い場合はガラ
スが結晶化しにくくなる。 P2O5が0.1%より少ない場合は、不均質な結晶
が析出してクラツクが入り易くなり、5%より多
い場合は、ガラスが分相すると共に失透し易くな
る。 Al2O3が1%より少ない場合は、ガラスが分相
し易くなり、10%より多い場合は、ガラスの溶融
が困難となる。 PbOは、ガラスマトリツクス相を安定にし、屈
伏点を低くするのに効果があるが、2.5%より少
ない場合は上記効果が得られず、10%より多い場
合はガラスが結晶化しにくくなる。 PbOが15%より多い場合は、ガラスが結晶化し
にくくなる。 B2O3が7%より多い場合は、結晶物にクラツ
クが入り易くなる。 また本発明の結晶化ガラスは、上記成分以外に
もZnO、MgO、CaO、BaO、SrO、ZrO2
TiO2、SnO2の各成分を5%まで添加することが
可能である。 上記の組成を有する本発明の磁気ヘツド用結晶
化ガラスは、屈伏点が630〜850℃と低いためヘツ
ド1,2のギヤツプ長やトラツク幅を変形させる
ことなく低温加熱によつて表面層のガラスマトリ
ツクス相を軟化させてヘツド1,2と良好な平行
度を保ちながらフエライトやセラミツクスを加圧
接着することができる。また熱膨張係数が85〜
135×10-7/℃であるため特にフエライトとの接
着に適している。 さらに本発明の磁気ヘツド用結晶化ガラスは、
研磨加工した後の表面粗度が300Å以下と小さく、
そのため接着性が良く、且つセンタースペーサ3
として用いた場合デイスクの磁気記録面を傷つけ
にくい。 以上の各特性を有する本発明の磁気ヘツド用結
晶化ガラスは、所望の大きさに切断研磨するだけ
で寸法精度に優れたセンタースペーサ3やスライ
ダー4を得ることが可能である。 実施例 以下実施例により本発明を説明する。 次表は、本発明に係るガラス組成及び屈伏点、
熱膨張係数、曲げ強度を示したものである。
INDUSTRIAL APPLICATION FIELD The present invention is a magnetic head suitable for pressure bonding members used in electronic component materials, particularly ferrite and ceramics of floppy disk drive heads used in computer recording devices, etc. It relates to crystallized glass. Prior Art In general, a head for a floppy disk drive, as shown in the drawing, consists of a recording/reproducing head 1 and an erasing head 2 made of ferrite, a center spacer 3 as a magnetic separation band made of ceramics, and a slider 4 for preventing head wear. The heads 1 and 2 each have a gap portion 5 and a reinforced glass 6. Conventionally, organic adhesives have been used to bond the heads 1 and 2 with the center spacer 3 and slider 4, but the head maintains precise relative positions with the center spacer 3 and slider 4 due to changes in temperature and humidity. 1 and 2 move,
Recently, sealing glass has been used in place of organic adhesives because of the problem of deterioration of properties. However, the sealing glass is susceptible to air bubbles entering the adhesive interface, and if air bubbles are present on the surface of heads 1 and 2 in particular, magnetic powder from the disk will settle there, damaging the magnetic recording surface of the disk and worsening the magnetic properties. There is a problem. In addition to ceramics, crystallized glass is also used for the slider 4, but because of its large surface roughness, it has poor adhesion to the heads 1 and 2, and when adhering to the heads 1 and 2 or the center spacer 3, adhesive must be used. was necessary. In other words, when crystallized glass is generally bonded directly to the heads 1 and 2 or the center spacer 3 using a slider, if the bonding temperature of the crystallized glass is higher than the sealing temperature of the gap portion 5, the organic adhesive of the gap portion 5 and the The sealing glass softens and tends to cause deformation in the gap length and track width of the completed heads 1 and 2, but the yield point of conventional crystallized glass is 850°C or higher, and when used as the slider 4, the bonding temperature This is because the temperature tends to be higher than the sealing temperature of the gap portion 5. Purpose of the Invention The invention was made in view of the above-mentioned problems, and it is possible to directly bond ferrite, ceramics, etc. with strong pressure by low-temperature heating without using an adhesive, as a member used for electronic component materials. The object of the present invention is to provide a crystallized glass for a magnetic head which has little foaming and high mechanical strength. Structure of the Invention The crystallized glass for a magnetic head of the present invention has a weight percentage of
So, SiO 2 60-85%, Li 2 O 7-15%, K 2 O 1-
7%, Na 2 O 0.1-7%, K 2 O + Na 2 O 2-14%,
P2O5 0.1 ~5%, Al2O3 1 ~10%, PbO 2.5~10
%, B 2 O 5 0 to 7%, and the total of the above components is 95% or more. The composition range of the crystallized glass for a magnetic head in the present invention is determined as described above for the following reasons. If SiO 2 is less than 60%, the chemical durability will be poor, and if it is more than 85%, the workability of the glass will be poor. If Li 2 O is less than 7%, the crystallinity will be low and the coefficient of thermal expansion will be high; if it is more than 15%, the crystallinity will be too high and the yield point will be too high. K 2 O and Na 2 O are effective in increasing the thermal expansion coefficient of crystallized glass, but if each is used alone, the glass matrix phase in crystallized glass contains a large amount of alkali components that are not crystal constituents, and the glass Since the matrix phase becomes unstable, in the present invention,
The glass matrix phase is stabilized by the mixed alkali effect caused by the coexistence of 1 to 7% K 2 O and 0.1 to 7% Na 2 O, and a crystallized glass with a low yield point can be obtained. When K 2 O is less than 1%, the yield point becomes too high, and when it is more than 7%, the glass becomes difficult to crystallize. If Na 2 O is less than 0.1%, the mixed alkali effect will not be exhibited and the yield point will be too high.
When it is more than 7%, the glass becomes difficult to crystallize. If the total amount of K 2 O and Na 2 O is less than 2%,
If the yield point becomes too high and exceeds 14%, the glass becomes difficult to crystallize. When P 2 O 5 is less than 0.1%, heterogeneous crystals are precipitated and cracks are likely to occur, and when it is more than 5%, the glass tends to undergo phase separation and devitrification. When Al 2 O 3 is less than 1%, the glass tends to undergo phase separation, and when it is more than 10%, it becomes difficult to melt the glass. PbO is effective in stabilizing the glass matrix phase and lowering the yield point, but if it is less than 2.5%, the above effects cannot be obtained, and if it is more than 10%, the glass becomes difficult to crystallize. If PbO is more than 15%, the glass becomes difficult to crystallize. When B 2 O 3 is more than 7%, cracks tend to form in the crystalline material. In addition to the above-mentioned components, the crystallized glass of the present invention also contains ZnO, MgO, CaO, BaO, SrO, ZrO 2 ,
It is possible to add up to 5% of each component of TiO 2 and SnO 2 . Since the crystallized glass for magnetic heads of the present invention having the above composition has a low yielding point of 630 to 850°C, the surface layer can be heated to a low temperature without changing the gap length or track width of the heads 1 and 2. By softening the matrix phase, ferrite or ceramics can be bonded under pressure while maintaining good parallelism with the heads 1 and 2. Also, the coefficient of thermal expansion is 85~
Since it has a temperature of 135×10 -7 /°C, it is particularly suitable for bonding with ferrite. Furthermore, the crystallized glass for magnetic heads of the present invention has
The surface roughness after polishing is less than 300Å,
Therefore, the adhesion is good and the center spacer 3
When used as a disc, it does not easily damage the magnetic recording surface of the disc. The crystallized glass for magnetic heads of the present invention having the above-mentioned characteristics can be used to obtain center spacers 3 and sliders 4 with excellent dimensional accuracy simply by cutting and polishing to a desired size. EXAMPLES The present invention will be explained below with reference to Examples. The following table shows the glass composition and yield point according to the present invention,
It shows the coefficient of thermal expansion and bending strength.

【表】【table】

【表】 表のNo.1〜4の試料は次のように調製した。 試料No.1〜4の各ガラス組成になるようにガラ
ス原料を調合し、白金ルツボを用いて1400〜1500
℃で5〜10時間溶融した後、溶融ガラスをカーボ
ン鋳型に流し込んで成形し、これを450〜500℃に
保持した電気炉内に入れて20〜30分保持した後室
温まで炉冷することによつてガラスを得た。次に
ガラスを電気炉中で500〜550℃までは120℃/時
の昇温速度で加熱し0.5〜1時間保持した後、700
〜900℃まで40℃/時の昇温速度で加熱し、0.5〜
5時間保持し、その後室温まで炉却した。得られ
た結晶化ガラスの主結晶相は、リチユムダイシリ
ケート(Li2O・2SiO2)、α−クリストバライト
(α−SiO2)であつた。 また上記の結晶化ガラスを10mm×20mm×40〜
80μに切断研磨して、両面をフエライトではさ
み、約600〜850℃で加熱しながら約1〜5Kg/cm2
の圧力を加えて接着した後、これを接着面に対し
垂直にダイヤモンドカツターで切断した。次にそ
の切断面を鏡面研磨した後、顕微鏡で観察したと
ころ接着部分には気泡、クラツクが認められず、
両者は強固に接着していた。 尚、表中の屈伏点は、周知のように熱膨張曲線
から求めたものであり、また曲げ強度は5φ×50
mmの無空棒状の結晶化ガラスを周知の三点荷重方
式によつて測定した。 発明の効果 以上のように本発明の磁気ヘツド用結晶化ガラ
スは、屈伏点が630〜850℃と低いため約600〜850
℃で加熱することによつてフエライトやセラミツ
クスと強固に加圧接着することができると共に発
泡が少なく機械的強度にも優れているため特にフ
ロツピーデイスクドライブ用ヘツドのセンタース
ペーサ3やスライダー4として適している。また
本発明の結晶化ガラスは、熱膨張係数が合う限り
フエライト以外のセンダスト、パーマロイ等の他
の合金材料と接着させることも可能である。
[Table] Samples No. 1 to 4 in the table were prepared as follows. Mix the glass raw materials to have the glass composition of Sample Nos. 1 to 4, and use a platinum crucible to
After melting at ℃ for 5 to 10 hours, the molten glass is poured into a carbon mold and shaped, placed in an electric furnace maintained at 450 to 500 ℃ for 20 to 30 minutes, and then cooled to room temperature. I twisted it and got some glass. Next, the glass was heated in an electric furnace to 500-550℃ at a heating rate of 120℃/hour, held for 0.5-1 hour, and heated to 700℃/hour.
Heating at a heating rate of 40℃/hour to ~900℃, 0.5~
It was held for 5 hours and then incinerated to room temperature. The main crystal phases of the obtained crystallized glass were lithium disilicate (Li 2 O.2SiO 2 ) and α-cristobalite (α-SiO 2 ). In addition, the above crystallized glass is 10mm x 20mm x 40 ~
Cut and polish to 80μ, sandwich both sides with ferrite, and heat at about 600 to 850℃ to produce about 1 to 5 kg/cm 2
After adhering by applying a pressure of Next, after mirror-polishing the cut surface, we observed it under a microscope and found no bubbles or cracks in the bonded area.
Both were firmly adhered. The yield point in the table is determined from the thermal expansion curve as is well known, and the bending strength is 5φ×50
A blank rod-shaped crystallized glass of mm was measured using a well-known three-point loading method. Effects of the Invention As described above, the crystallized glass for magnetic heads of the present invention has a low yielding point of 630 to 850°C,
By heating at ℃, it can be firmly bonded to ferrite or ceramics under pressure, and it also has low foaming and excellent mechanical strength, making it particularly suitable as the center spacer 3 and slider 4 of floppy disk drive heads. ing. Further, the crystallized glass of the present invention can be bonded to other alloy materials other than ferrite, such as sendust and permalloy, as long as the coefficients of thermal expansion match.

【図面の簡単な説明】[Brief explanation of drawings]

図面は、フロツピーデイスクドライブ用ヘツド
の平面図である。 1…記録再生ヘツド、2…消去ヘツド、3…セ
ンタースペーサ、4…スライダー、5…ギヤツプ
部、6…補強ガラス。
The drawing is a plan view of a floppy disk drive head. DESCRIPTION OF SYMBOLS 1... Recording/reproducing head, 2... Erasing head, 3... Center spacer, 4... Slider, 5... Gap portion, 6... Reinforced glass.

Claims (1)

【特許請求の範囲】[Claims] 1 重量%で、SiO2 60〜85%、Li2O 7〜15%、
K20 1〜7%、Na2O 0.1〜7%、K2O+Na2O
2〜14%、P2O5 0.1〜5%、Al2O3 1〜10%、
PbO 2.5〜10%、B2O3 0〜7%を含有し、且つ
上記成分の合計が95%以上であり、屈伏点が630
〜850℃、30〜500℃の熱膨張係数が85〜135×
10-7/℃であることを特徴とする磁気ヘツド用結
晶化ガラス。
1% by weight, SiO 2 60-85%, Li 2 O 7-15%,
K 2 O 1-7%, Na 2 O 0.1-7%, K 2 O + Na 2 O
2-14%, P2O5 0.1-5 %, Al2O3 1-10 %,
Contains 2.5 to 10% PbO, 0 to 7% B2O3 , and the total of the above components is 95% or more, and the yield point is 630.
~850℃, 30~500℃ thermal expansion coefficient 85~135×
A crystallized glass for magnetic heads characterized by a temperature of 10 -7 /℃.
JP9037086A 1986-04-18 1986-04-18 Crystallized glass Granted JPS62246840A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9037086A JPS62246840A (en) 1986-04-18 1986-04-18 Crystallized glass

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9037086A JPS62246840A (en) 1986-04-18 1986-04-18 Crystallized glass

Publications (2)

Publication Number Publication Date
JPS62246840A JPS62246840A (en) 1987-10-28
JPH0428660B2 true JPH0428660B2 (en) 1992-05-14

Family

ID=13996670

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9037086A Granted JPS62246840A (en) 1986-04-18 1986-04-18 Crystallized glass

Country Status (1)

Country Link
JP (1) JPS62246840A (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0629152B2 (en) * 1987-02-26 1994-04-20 株式会社オハラ Method for producing crystallized glass for substrate
JPH01138151A (en) * 1987-11-24 1989-05-31 Matsushita Electric Ind Co Ltd magnetic head
JPH0794291B2 (en) * 1988-04-02 1995-10-11 村樫石灰工業株式会社 Transfer method of powder and granular material
KR100324266B1 (en) * 1999-07-19 2002-02-25 구자홍 Composition of Thick Film Dielectric for Solid State Display Device
WO2014055834A1 (en) 2012-10-04 2014-04-10 Corning Incorporated Article with glass layer and glass-ceramic layer and method of making the article
TWI679108B (en) 2012-10-04 2019-12-11 美商康寧公司 Laminated glass article with ceramic phase and method of making the article
US10202303B2 (en) 2012-10-04 2019-02-12 Corning Incorporated Compressively stressed laminated glass article via photosensitive glass and method of making the article
CN107265863A (en) * 2017-08-02 2017-10-20 宜兴市金鱼陶瓷有限公司 A kind of celadon with iron oxide red gold ring glaze layer and preparation method thereof

Also Published As

Publication number Publication date
JPS62246840A (en) 1987-10-28

Similar Documents

Publication Publication Date Title
JP3140702B2 (en) Crystallized glass for magnetic disk substrate, magnetic disk substrate and magnetic disk
KR100188901B1 (en) A glass-ceramic substrate for a magnetic disk
JP4785274B2 (en) Glass article and glass substrate for magnetic recording medium using the same
JPH07300340A (en) Crystallized glass for information-recording disk
JP4086210B2 (en) Substrate for information recording medium
JPH0428660B2 (en)
JP2000103636A (en) High-modulus glass and glass ceramic
US4794483A (en) Magnetic head having layers of amorphous magnetic alloy bonded together with a glass containing vandium oxide phosphorus oxide and antimony oxide
JP7276645B2 (en) Glass substrate for magnetic recording media
EP0254198B1 (en) Sealing glass
JP2005247602A (en) Glass composition and magnetic head
JPS63210039A (en) Production of crystallized glass for substrate
JPS6163542A (en) Crystallized glass having high thermal expansion coefficient and its preparation
JP4273620B2 (en) Substrate glass
JP7698241B2 (en) Glass disk for magnetic recording medium and magnetic recording device using same
JP2821182B2 (en) Electronic component manufacturing method
JP3152905B2 (en) Crystallized glass substrate for magnetic disk
JP2740697B2 (en) Moisture resistant low melting glass composition for magnetic head and magnetic head
JPS6360127A (en) High-hardness and high-expansive crystallized glass
JPH0826769A (en) Glass for bonding magnetic head
JPH07129909A (en) Glass for magnetic head and magnetic head
JPH0543269A (en) Crystallized glass
JPS61186246A (en) Glass composition having high expansion coefficient
JP2002145641A (en) Crystallized glass substrate for information recording medium
JPH0761836A (en) Glass for adhering ferrite