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JPH0633166B2 - Porcelain composition for magnetic head - Google Patents
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JPH0633166B2 - Porcelain composition for magnetic head - Google Patents

Porcelain composition for magnetic head

Info

Publication number
JPH0633166B2
JPH0633166B2 JP60192889A JP19288985A JPH0633166B2 JP H0633166 B2 JPH0633166 B2 JP H0633166B2 JP 60192889 A JP60192889 A JP 60192889A JP 19288985 A JP19288985 A JP 19288985A JP H0633166 B2 JPH0633166 B2 JP H0633166B2
Authority
JP
Japan
Prior art keywords
thermal expansion
porcelain
magnetic head
ferrite
slider
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 - Lifetime
Application number
JP60192889A
Other languages
Japanese (ja)
Other versions
JPS6252167A (en
Inventor
克彦 鬼塚
秀雄 江村
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.)
Kyocera Corp
Original Assignee
Kyocera Corp
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 Kyocera Corp filed Critical Kyocera Corp
Priority to JP60192889A priority Critical patent/JPH0633166B2/en
Publication of JPS6252167A publication Critical patent/JPS6252167A/en
Publication of JPH0633166B2 publication Critical patent/JPH0633166B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)
  • Adjustment Of The Magnetic Head Position Track Following On Tapes (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はフロッピーディスク等の磁器ヘッドに使用され
る磁極片(フェライトコア)を支持する磁気ヘッド用磁
器(以下スライダと称す)の磁器組成物に関するもので
あり、更に詳しくはMn−Znフェライトに適した磁気ヘッ
ドスライダの磁器組成物に関する。
The present invention relates to a porcelain composition for a magnetic head porcelain (hereinafter referred to as a slider) for supporting a magnetic pole piece (ferrite core) used in a porcelain head such as a floppy disk. And more particularly to a porcelain composition of a magnetic head slider suitable for Mn-Zn ferrite.

(背景技術) 図に示す如く前記スライダ1は一般にフェライトコア2
を接着ガラス3を介して熱処理により接着して磁気ヘッ
ドを構成している。したがって、これらスライダ1及び
フェライトコア2の各々に大きな熱膨張等があると熱処
理時の熱履歴により、これら材料に亀裂や残留歪が生じ
組付け工程中にガラスハガレ等を生じる。そのため、ス
ライダ1はその磁器組成及び組成比を選択してフェライ
トコア2の熱膨張係数に一致させなければならない。
(Background Art) As shown in the figure, the slider 1 is generally a ferrite core 2
Are bonded by heat treatment through the adhesive glass 3 to form a magnetic head. Therefore, if each of the slider 1 and the ferrite core 2 has a large thermal expansion or the like, a thermal history during heat treatment causes cracks or residual strains in these materials, causing glass peeling or the like during the assembling process. Therefore, the slider 1 must select its porcelain composition and composition ratio to match the thermal expansion coefficient of the ferrite core 2.

また、フェライトコアにはその用途に応じ各種のグレー
ドが存在し熱膨張係数もこのグレードにより105 〜140
×10-7/℃の広い範囲に適用される必要がある。そのた
め、スライダもその組成比を変化させることにより105
〜140 ×10-7/℃の広い範囲の熱膨張係数を容易に選択
されることが望まれている。
There are various grades of ferrite cores depending on their use, and the thermal expansion coefficient is 105 to 140 depending on this grade.
It needs to be applied to a wide range of × 10 -7 / ° C. Therefore, by changing the composition ratio of the slider, 105
It is desired to easily select a wide range of thermal expansion coefficient of ˜140 × 10 −7 / ° C.

また、スライダはその磁器焼結体にポアが出来るだけ少
ないことが要求される。フロッピーディスクに接触する
焼結体表面にポアが多く存在すると、該ディスク表面に
コーディングされた磁性粉末がポア内に付着し易くな
り、付着した磁性粉の存在により記録再生時の磁気特性
に障害をもたらす。
Further, the slider is required to have as few pores as possible in the porcelain sintered body. If there are many pores on the surface of the sintered body that comes into contact with the floppy disk, the magnetic powder coded on the disk surface will easily adhere to the pores, and the presence of the adhered magnetic powder will impair the magnetic characteristics during recording and reproduction. Bring

また、スライダはその磁器が充分に焼結し緻密化してい
なければならない。焼結が不充分で強度や靭性が劣って
いると磁器にチッピングやクラックが発生し、フロッピ
ーディスクへ走行させた場合ディスク自体を損傷させる
という重大な欠陥をまねく。
Further, the slider must have its porcelain sufficiently sintered and densified. If the sintering is insufficient and the strength and toughness are inferior, chipping and cracks will occur in the porcelain, leading to a serious defect that the disk itself will be damaged when running on a floppy disk.

一方、磁気ヘッドのコアとしては従来からNi−Znフェラ
イトが使用されていたがプロッピディスク用フェライト
コアとしてはNi−ZnよりMn−Znフェライトの方が磁性特
性、特に抗磁力が優れていることから、Mn−Znフェライ
トに移行しつつある。
On the other hand, Ni-Zn ferrite has been conventionally used as the core of the magnetic head, but Mn-Zn ferrite has better magnetic characteristics, especially coercive force than Ni-Zn as the ferrite core for the prop disk. Since then, it is shifting to Mn-Zn ferrite.

(従来技術の説明) 従来Ni−Znフェライトに適用されるスライダ組成物とし
てはこの熱膨張係数90〜98×10-7/℃とほぼ同程度のフ
ォルステアライトやチタン酸バリウムが知られている。
しかしながら、Mn−Znフェライトにこれら磁器を適用す
る場合、Mn−Znフェライトの熱膨張係数が105 〜140 ×
10-7/℃であり熱膨張差が大きすぎこれら磁器を適用す
ることは困難である。
(Explanation of Prior Art) Forsterite or barium titanate having a thermal expansion coefficient of about 90 to 98 × 10 −7 / ° C. is known as a slider composition conventionally applied to Ni—Zn ferrite. .
However, when these porcelains are applied to Mn-Zn ferrite, the thermal expansion coefficient of Mn-Zn ferrite is 105 to 140 ×
Since it is 10 −7 / ° C. and the difference in thermal expansion is too large, it is difficult to apply these porcelains.

一方、Mn−Znフェライトに適用するスライダ組成物
としては従来からチタン酸塩系化合物を主体とする例え
ばチタン酸カルシウム、チタン酸マグネシウム及びチタ
ン酸ストロンチウム等がMn−Znフェライトの熱膨張係数
とほぼ同程度であることが知られている。しかしなが
ら、Mn−Znフェライトは要求特性に応じて105 〜140 ×
10-7/℃の広い範囲で多種多様のグレードが存在する
が、従来からこの広い範囲の熱膨張係数を組成比を変更
するのみで直線的に変化させ各種グレードの熱膨張係数
に容易に一致させる磁気ヘッド用スライダ組成物が見出
されていない。
On the other hand, as a slider composition applied to Mn-Zn ferrite, for example, calcium titanate, magnesium titanate, and strontium titanate, which mainly contain a titanate compound, have the same thermal expansion coefficient as that of Mn-Zn ferrite. It is known to be degree. However, Mn-Zn ferrite is 105 to 140 × depending on the required characteristics.
There are a wide variety of grades in a wide range of 10 -7 / ° C. Conventionally, the thermal expansion coefficient of this wide range can be linearly changed by simply changing the composition ratio and easily match the thermal expansion coefficient of various grades. No magnetic head slider composition has been found.

一方、近時スライダ用磁器焼結体のポア、特に大きな径
のポアの発生を少なくするために常圧焼成又はホットプ
レスにより得られた焼結体をさらにHIP(熱間静水圧
プレス)処理することが試られている。ところが、前記
チタン酸塩系化合物を主体とする組成においては例えば
アルゴンガス中で焼成した場合にTiイオンが還元され
るため極端に磁器の色調が変化する。この場合変化した
磁器の色を元に戻す処理が必要となる。
On the other hand, recently, in order to reduce the generation of pores in the porcelain sintered body for sliders, especially pores of large diameter, the sintered body obtained by normal pressure firing or hot pressing is further subjected to HIP (hot isostatic pressing) treatment. Is being tested. However, in the composition mainly containing the titanate compound, the color tone of the porcelain is extremely changed because Ti ions are reduced when firing in argon gas, for example. In this case, it is necessary to restore the changed color of the porcelain.

(本発明が解決しようとする問題点) 本発明者は上記現状に鑑み鋭意研究の結果、BaO及びSiO
2を主成分とし、これに対しTiO2,MgO,ZnO及びZrO2
ら選ばれる少量の添加剤を含む磁気ヘッド用磁器組成物
は熱膨張係数が 105〜 140×10-7/℃の範囲で自由に選
択できかつボイド発生率及び焼結性に優れていると共
に、HIP処理した場合に色調変化の少ないことを見い
出した。
(Problems to be solved by the present invention) As a result of earnest research in view of the above-mentioned present situation, the present inventors have found that BaO and SiO
2 is the main component, on the other hand, a ceramic composition for a magnetic head containing a small amount of an additive selected from TiO 2 , MgO, ZnO and ZrO 2 has a thermal expansion coefficient of 105 to 140 × 10 -7 / ° C. It was found that they can be freely selected, have an excellent void generation rate and excellent sinterability, and have little change in color tone when subjected to HIP treatment.

(発明の目的) 本発明は各種要求特性に応じたMn−Znフェライトの磁器
ヘッドの熱膨張係数の広い範囲に容易に適応できかつボ
イドの発生が少なく焼結性に優れると共に、HIP処理し
た場合に焼結体の色調変化の少ない磁気ヘッド用磁器組
成物を提供することを目的とする。
(Object of the Invention) The present invention can be easily adapted to a wide range of the thermal expansion coefficient of the porcelain head of Mn-Zn ferrite according to various required characteristics, has less voids and is excellent in sinterability, and when subjected to HIP treatment. Another object of the present invention is to provide a porcelain composition for a magnetic head, in which the color tone of the sintered body is small.

(問題を解決するための手段) 本発明はBaOを37〜50モル%と、SiO2を50〜63モル%と
からなる主成分100 重量部に対して、TiO2,MgO,ZnO及
びZrO2から選ばれる少なくとも1種を15重量部以下(0
を含まず)添加してなる磁気ヘッド用磁器組成物が提供
される。
(Means for Solving the Problem) The present invention is based on 100 parts by weight of a main component consisting of 37 to 50 mol% of BaO and 50 to 63 mol% of SiO 2 , TiO 2 , MgO, ZnO and ZrO 2 15 parts by weight or less (0
A ceramic composition for a magnetic head is provided.

上記範囲内でBaO,SiO2の成分割合を変化させることに
よって熱膨張係数を 105〜 140×10-7/℃の範囲で自由
に選択することができる。
The thermal expansion coefficient can be freely selected within the range of 105 to 140 × 10 -7 / ° C by changing the composition ratio of BaO and SiO 2 within the above range.

また、雰囲気によって価数の変化を受けにくいBaO及びS
iO2を主成分としているため、HIP処理に伴う色調変
化がない。
In addition, BaO and S are less susceptible to changes in valence depending on the atmosphere.
Since iO 2 is the main component, there is no change in color tone due to HIP processing.

BaO及びSiO2の量比を上記範囲に限定する理由と
してはBaOが50モル%を超えると、磁器中に未反応のBaO
が存在し易く、磁器自体の耐湿性が劣化する等のスライ
ダ用磁器として不安定となる。また、BaOが37モル%未
満及びSiO2が63モル%を超えると、SiO2相が生成
して熱膨張係数の低下が大きくなる。
The reason for limiting the amount ratio of BaO and SiO 2 to the above range is that when BaO exceeds 50 mol%, unreacted BaO in the porcelain is present.
Is easily present, and the moisture resistance of the porcelain itself is deteriorated, which makes it unstable as a slider porcelain. When BaO is less than 37 mol% and SiO 2 is more than 63 mol%, a SiO 2 phase is formed and the thermal expansion coefficient is greatly reduced.

TiO2,MgO,ZnO及びZrO2の少なくとも1種を添加するこ
とはBaO−SiO2系の焼結性を促進させるものであるが、
これらを添加すると焼成温度を低下させることができ、
ポアの発生を低減させることができる。但し、上記添加
物の少なくとも1種を15重量%を超えて添加した場合、
熱膨張係数は 105×10-7/℃未満となり本発明からは除
外される。
Although the addition of at least one of TiO 2 , MgO, ZnO and ZrO 2 promotes the sinterability of the BaO-SiO 2 system,
By adding these, the firing temperature can be lowered,
The generation of pores can be reduced. However, when at least one of the above additives is added in excess of 15% by weight,
The coefficient of thermal expansion is less than 105 × 10 −7 / ° C. and is excluded from the present invention.

以下、実施例により本発明を詳細に説明する。Hereinafter, the present invention will be described in detail with reference to examples.

本発明においては磁気ヘッド用スライダを製作する方法
は所定の組成比に原料を秤量し、混合粉砕後、仮焼し、
次いでこの仮焼物を微粉砕し、有機バインダを添加して
造粒し、所定寸法に成形後焼成する通常の方法が採用す
れば、より緻密質な焼結体が得られるので好ましい。
In the present invention, the method of manufacturing a slider for a magnetic head is to weigh raw materials in a predetermined composition ratio, mix and pulverize, and then calcine,
Next, it is preferable to employ a usual method in which the calcined product is finely pulverized, an organic binder is added to granulate, and the mixture is molded into a predetermined size and then fired, since a denser sintered body can be obtained.

(実施例1) 市販されているBaCo3,SiO2,TiO2,Mg(OH)2,CoCO3
及びZrO2を用いて焼結後の磁器組成を第1表に示すよう
に秤量し、ボールミルを用いて湿式混合した。これを乾
燥させ、乾燥後の原料を 950〜1150℃の温度範囲で1〜
2時間仮焼を行った。仮焼後の原料を不純物の混入を抑
えて平均粒径約1.5 μm以下になるように微粉砕した。
これに有機バインダー等を加えて造粒を行った後1.0 〜
2.0ton/cm2の圧力で成形した。本焼成は1200〜1450℃
の温度範囲で1.0 〜2.0 時間大気中で行い、第1表に示
すNo.1〜9の各試料を得た。
Example 1 Commercially available BaCo 3 , SiO 2 , TiO 2 , Mg (OH) 2 and CoCO 3
The porcelain composition after sintering was weighed as shown in Table 1 using ZrO 2 and ZrO 2 , and wet-mixed using a ball mill. This is dried, and the raw material after drying is heated in the temperature range of 950 to 1150 ° C.
It was calcined for 2 hours. After the calcination, the raw material was finely pulverized so that the mixture of impurities was suppressed and the average particle diameter was about 1.5 μm or less.
After adding an organic binder to this and granulating, 1.0 ~
Molded at a pressure of 2.0 ton / cm 2 . Main firing is 1200-1450 ℃
Samples Nos. 1 to 9 shown in Table 1 were obtained by performing the heating in the atmosphere in the temperature range of 1.0 to 2.0 hours.

得られた磁器について適正焼成温度、嵩比重、40〜400
℃における平均熱膨張係数、ポア分布及び焼結性につい
て調べ第1表に列記した。適正焼成温度は嵩比重が最大
となる温度とした。ポア発生率は1μmのダイヤモンド
砕粒による最終ラップ面(鏡面)に占めるポアの占有面
積を測定することにより評価した。測定は(×200 )の
倍率下で画像解析装置を用いて行い全測定面積に対する
ポアの占有面積の割合で示した。この値が2%以上を
×,1〜2%を△,0.1 〜1%を○, 0.1%以下を◎の
記号で示した。焼結性については吸水率2%以上を×,
0%を○,その中間を△の記号で示した。
Proper firing temperature, bulk specific gravity, 40-400 for the obtained porcelain
The average coefficient of thermal expansion at ℃, pore distribution and sinterability were investigated and listed in Table 1. The appropriate firing temperature was the temperature at which the bulk specific gravity was maximum. The pore generation rate was evaluated by measuring the area occupied by pores in the final lap surface (mirror surface) formed by 1 μm crushed diamond particles. The measurement was performed using an image analyzer under a magnification of (× 200), and it was shown as the ratio of the area occupied by pores to the total measured area. When this value is 2% or more, x is shown, 1-2% is indicated by Δ, 0.1-1% is indicated by o, and 0.1% or less is indicated by o. Regarding sinterability, water absorption of 2% or more is ×,
The symbol 0 indicates 0% and the middle symbol indicates Δ.

第1表から理解されるように試料No.3〜7は本発明の
範囲内のものであり、夫々熱膨張係数は 105〜140 ×10
-7/℃の範囲に選ばれており、ポアの発生率及び焼結性
が良好である。これに対し試料No.1及び2はTiO2,Mg
O,ZnO,ZrO2又はCaOが無添加の場合でありポア発生率
及び焼結性が悪化している。試料No.1は主成分中のB
aOが若干多い場合であり、耐湿性が劣化しスライダと
して不安定となるため、熱膨張係数は 143×10-7/℃と
大きくなっている。試料No.8はSiO2が多い場合であり
熱膨張係数の低下が大きい。試料No.9はTiO2の添加が
多い場合であり熱膨張係数が低下している。
As can be seen from Table 1, Sample Nos. 3 to 7 are within the scope of the present invention, and the thermal expansion coefficients thereof are 105 to 140 × 10 5, respectively.
It is selected in the range of -7 / ° C, and the rate of pore generation and sinterability are good. On the other hand, sample Nos. 1 and 2 are TiO 2 , Mg
When O, ZnO, ZrO 2 or CaO was not added, the pore generation rate and sinterability deteriorate. Sample No. 1 is B in the main component
In the case where aO is a little large, the moisture resistance deteriorates and the slider becomes unstable, so that the thermal expansion coefficient is as large as 143 × 10 −7 / ° C. Sample No. 8 had a large amount of SiO 2 and had a large decrease in the coefficient of thermal expansion. Sample No. 9 had a large addition of TiO 2 and had a low coefficient of thermal expansion.

(実施例2) 前記第1表に示す各試料についてHIP処理を行った。HIP
処理については1000〜1200℃、2000kg/cm2でアルゴン
雰囲気中で1〜2時間焼成した。これらについてHIP後
の比重、HIP前の比重とのアップ率及び色調の変化率に
ついて計算及び目視により観察し、ポア発生率について
は実施例1と同様に評価して第2表に示した。
Example 2 The samples shown in Table 1 were subjected to HIP treatment. HIP
Regarding the treatment, it was baked at 1000 to 1200 ° C. and 2000 kg / cm 2 in an argon atmosphere for 1 to 2 hours. The specific gravity after HIP, the up ratio with respect to the specific gravity before HIP and the rate of change in color tone were calculated and visually observed, and the pore generation rate was evaluated in the same manner as in Example 1 and shown in Table 2.

各試料共にHIP後の比重は2%程度向上しており、試料N
o.1及び2を除いてはポア発生率は非常に少なく良好で
ある。しかしながら試料No.9はTiO2が多く添加され
ているためにHIP後の焼結体の色調が白色から青色に変
化している。
The specific gravity of each sample after HIP has improved by about 2%.
Except for o.1 and 2, the pore generation rate is very small and good. However, in Sample No. 9, the color tone of the sintered body after HIP changed from white to blue because TiO 2 was added in a large amount.

(実施例3) TiO2を64重量%とCaOを36重量%とを混合したチタン酸
塩化合物を主体とした混合粉体を実施例1及び2と同様
の方法にて仮焼−通常焼成−HIP処理を行ったところ
HIP後の焼結体の色調は淡褐色から黒色に変化してい
た。
Example 3 A mixed powder mainly composed of a titanate compound in which 64% by weight of TiO 2 and 36% by weight of CaO are mixed is calcined by the same method as in Examples 1 and 2 -normal firing- When HIP processing was performed, the color tone of the sintered body after HIP changed from light brown to black.

上記の如く本発明のBaO−SiO2系磁器組成物はTiO2,Mg
O,ZnO及びZrO2の少なくとも1種の焼結促進剤を若干量
混合することにより、熱膨張係数の 105〜 140×10-7
℃の広い範囲を任意に選択できると共に、ポアが少なく
かつ焼結性が良好である。また焼結体のポア径を小さく
又はポアを少なくするためにHIP処理を行っても、焼
結体の色調変化がなく商品価値を低減させることがな
い。
As described above, the BaO—SiO 2 porcelain composition of the present invention contains TiO 2 , Mg
By mixing a small amount of at least one sintering promoter of O, ZnO and ZrO 2 , a thermal expansion coefficient of 105 to 140 × 10 -7 /
A wide range of ° C can be arbitrarily selected, the pores are small and the sinterability is good. Further, even if HIP treatment is performed to reduce the pore diameter of the sintered body or reduce the pores, the color tone of the sintered body does not change and the commercial value is not reduced.

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

図面はフロッピーディスクに使用される磁気ヘッドの斜
視図である。
The drawing is a perspective view of a magnetic head used for a floppy disk.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】BaOを37〜50モル%と、SiO2を50〜63モル
%とからなる主成分100 重量部に対して、TiO2,MgO,Z
nO及びZrO2から選ばれる少なくとも1種を15重量部以下
(0を含まず)添加してなる磁気ヘッド用磁器組成物。
1. TiO 2 , MgO, Z based on 100 parts by weight of the main component consisting of 37 to 50 mol% of BaO and 50 to 63 mol% of SiO 2.
A porcelain composition for a magnetic head, comprising 15 parts by weight or less (not including 0) of at least one selected from nO and ZrO 2 .
JP60192889A 1985-08-30 1985-08-30 Porcelain composition for magnetic head Expired - Lifetime JPH0633166B2 (en)

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JP60192889A JPH0633166B2 (en) 1985-08-30 1985-08-30 Porcelain composition for magnetic head

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Application Number Priority Date Filing Date Title
JP60192889A JPH0633166B2 (en) 1985-08-30 1985-08-30 Porcelain composition for magnetic head

Publications (2)

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JPS6252167A JPS6252167A (en) 1987-03-06
JPH0633166B2 true JPH0633166B2 (en) 1994-05-02

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JPS6252167A (en) 1987-03-06

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