JPS62288132A - Production of magnetic head - Google Patents

Production of magnetic head

Info

Publication number
JPS62288132A
JPS62288132A JP12965986A JP12965986A JPS62288132A JP S62288132 A JPS62288132 A JP S62288132A JP 12965986 A JP12965986 A JP 12965986A JP 12965986 A JP12965986 A JP 12965986A JP S62288132 A JPS62288132 A JP S62288132A
Authority
JP
Japan
Prior art keywords
glass
magnetic head
gap
magnetic
mol
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.)
Pending
Application number
JP12965986A
Other languages
Japanese (ja)
Inventor
Masato Yamashita
山下 真郷
Ryuzo Higashihara
隆三 東原
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP12965986A priority Critical patent/JPS62288132A/en
Publication of JPS62288132A publication Critical patent/JPS62288132A/en
Pending 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
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/062Glass compositions containing silica with less than 40% silica by weight
    • C03C3/07Glass compositions containing silica with less than 40% silica by weight containing lead
    • C03C3/072Glass compositions containing silica with less than 40% silica by weight containing lead containing boron

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

Abstract

PURPOSE:To obtain a magnetic head having improved environmental resistance without deteriorating magnetic characteristic, by melting and permeating a glass composition, consisting essentially of Bi2O3, SiO2 and B2O3 of specific composition for joining magnetic heads into a magnetic head gap part. CONSTITUTION:A glass rod 3 is obtained from a glass composition, consisting of a principal component, consisting of (A) 13-30mol% Bi2O3, (B) 30-50mol% SiO2 and (C) 1-20mol% B2O3 and satisfying the relationship of >45mol% total of the components (B) and (C) and >2 molar ratio (B/C) and (D) one or more of 1-20mol% Li2O, 1-18mol% Na2O or 1-10mol% K2O and used for joining magnetic heads. The above-mentioned glass rod 3 is then placed on each gap groove 4 of a cut part 2 machined to form a given magnetic passage in a ferrite block 1 and melted while heating at a temperature to give 10<2.5>-10<3>P glass viscosity thereof and then melted, permeated ad adhered to the gap groove 4. The resultant magnetic head member 10 is then cut at each part of a chain line 5 to give a magnetic head front core part 6, which is then bonded to a back core 7, ground and finished to a position of a chain line 8.

Description

【発明の詳細な説明】 3、発明の詳細な説明 産業上の利用分野 本発明は磁気ヘッドの製造方法に関するものである。[Detailed description of the invention] 3. Detailed description of the invention Industrial applications The present invention relates to a method of manufacturing a magnetic head.

従来の技術 フェライト磁気ヘッドのギャップ部に用いる非磁性スペ
ーサーとしては、媒体との摺動に際してギャップ近傍に
機械的くずれが生じたり、ヘッドコアの摩耗度合に比し
て極度にギャップ部が摩耗することがないように、硬度
が高(耐摩耗性に優れたガラス材を用いることが広く行
われている。
Conventional technology Non-magnetic spacers used in the gap portion of ferrite magnetic heads do not cause mechanical deformation near the gap when sliding with the medium, or wear out of the gap portion to an extreme degree compared to the degree of wear of the head core. It is widely practiced to use a glass material with high hardness (excellent abrasion resistance) to prevent the wear and tear from occurring.

このガラスギャップ形成法には、浸透法の他にスパッタ
法、焼付法等が知られているが、交流消去ヘッドのごと
くギャップ幅が数十μm以上も必要とされる場合は、浸
透法を用いるのが通例である。
In addition to the infiltration method, sputtering and baking methods are known to form this glass gap, but in cases where a gap width of several tens of micrometers or more is required, such as in an AC erasing head, the infiltration method is used. It is customary.

七ころで、通常行われている浸透法による消去ヘッドの
ガラスギャップ形成法は、第1図及び第2図に示したご
とくフェライトブロック1を所定の形状に加工し切り込
み部2を設け、更にこの部分に所望の寸法のギャップ溝
4を入れ、その溝4の上にギャップ用ガラス棒3を設置
して溶融、浸透させることによりガラスギャップを形成
するといったものであった。
The glass gap forming method for the erasing head, which is usually carried out by the penetration method, is to process a ferrite block 1 into a predetermined shape and provide a notch 2, as shown in FIGS. 1 and 2. A gap groove 4 of a desired size is formed in the part, and a glass gap rod 3 is placed on top of the groove 4 and melted and infiltrated to form a glass gap.

その際、用いられるガラスは熱膨張係数がフェライトコ
アとほぼ同一のものにしないと、接着部の界面近傍に固
着後歪が残り磁気特性を劣化させたり、甚だしい場合は
、ガラスあるいはフェライトにクラックが入り破壊され
てしまうことがある。
In this case, unless the glass used has a coefficient of thermal expansion that is almost the same as that of the ferrite core, strain may remain after adhesion near the interface of the bonded part, deteriorating the magnetic properties, or in severe cases, cracks may occur in the glass or ferrite. It may be destroyed by entering.

また磁気記録に用いられる記録媒体は近年の高密度記録
化の進展に伴い高保磁力化してきており、これら高保磁
力媒体を消去する消去ヘッドに於いては大きな交流消去
磁界を発生させねばならないため、電気抵抗が高いフェ
ライトそれも飽和磁束密度が比較的高いMn−Zn系の
ものが用いられている。そして一般に知られているよう
に、Mn−Zn系フェライトで飽和磁束密度を高くする
組成を選択すると熱膨張係数は大きくなる。
In addition, the recording media used for magnetic recording have become higher in coercive force due to the recent progress in high-density recording, and the erasing heads that erase these high-coercive-force media must generate a large alternating current erasing magnetic field. Ferrites with high electrical resistance and Mn--Zn type ferrites with relatively high saturation magnetic flux density are used. As is generally known, when a composition of Mn-Zn ferrite that increases the saturation magnetic flux density is selected, the coefficient of thermal expansion increases.

従って、高飽和磁束密度フェライトに熱膨張係数を合わ
せるため、消去ヘッドのギャップ形成にはPbOを大量
に含有するアルカリ珪酸塩ガラス(PbO−81o2−
R20)が広く用いられている。
Therefore, in order to match the coefficient of thermal expansion to high saturation magnetic flux density ferrite, the gap of the erase head is formed using alkali silicate glass (PbO-81o2-) containing a large amount of PbO.
R20) is widely used.

発明が解決しようとする問題点 しかしながらPbOを大量に含有するガラスでギャップ
を形成したヘッドを、湿度の高い環境下に放置した場合
、ギャップ部が腐食(風化)し始め、接着強度を低下さ
せるのみならず、腐食により発生した突起物により記録
媒体を損傷させたり、腐食物が剥離した空孔部分に媒体
の磁性粉が付着しノイズを発生させたりするという問題
点があった。さらにPbOを大量に含有するガラスは低
融点、低粘度で拡散係数が大きいため、ガラス作業温度
で溶融ガラスがフェライト粒界へ拡散し磁気特性を劣化
させるおそれがあった。
Problems to be Solved by the Invention However, if a head with a gap made of glass containing a large amount of PbO is left in a humid environment, the gap will begin to corrode (weather), which will only reduce the adhesive strength. Moreover, there are problems in that the recording medium is damaged by protrusions generated by corrosion, and magnetic powder from the medium adheres to the voids where corroded substances have peeled off, causing noise. Furthermore, since glass containing a large amount of PbO has a low melting point, low viscosity, and a large diffusion coefficient, there is a risk that the molten glass will diffuse into the ferrite grain boundaries at glass working temperatures, deteriorating the magnetic properties.

そこで本発明は、耐環境性の優れた、特性劣化の少ない
磁気ヘッドを提供することを目的とする。
SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a magnetic head with excellent environmental resistance and less deterioration of characteristics.

問題点を解決するための手段 上記した従来の問題点を解決するため、本発明はB i
 203.S io2.B2O3の3成分を主成分とし
、且つそれぞれを Bi2O3:  13〜30(mo+!%)SiO2 
  :  30〜50(mol%)B2O3:    
 1〜20 (mo 2%)の範囲内で、しかも SiOS102(%)+B2O3:(mol%)>45
(moffi%) SiO2(mol%)/B2O3(mol%)〉2 なる関係式を満足するよう含有し、また残部にLi 2
0.Na 2O、K2O.のうち少なくとも1種をそれ
ぞれ 1i2Q  :  1〜20(mol%)Na20  
:  1〜18(mol%)K2O:   1〜10(
mol%) の範囲内で含有するガラス組成物を用いて、しか2.5 もそのガラス組成物の粘度が10  ポイズから103
ポイズとなる温度範囲内で磁気ギャップ部に溶融、浸透
させて磁気ヘッドを製造する。
Means for Solving the Problems In order to solve the above-mentioned conventional problems, the present invention provides B i
203. Sio2. The three main components are B2O3, and each of them is Bi2O3: 13-30 (mo+!%) SiO2
: 30-50 (mol%) B2O3:
Within the range of 1 to 20 (mo 2%), and SiOS102 (%) + B2O3: (mol%) > 45
(moffi%) SiO2 (mol%)/B2O3 (mol%)〉2.
0. Na2O, K2O. At least one of the following: 1i2Q: 1 to 20 (mol%) Na20
: 1-18 (mol%) K2O: 1-10 (
mol%) within the range of 2.5 to 103 mol%.
A magnetic head is manufactured by melting and infiltrating the magnetic gap within a temperature range that produces a poise.

なお上記ガラス組成物において、B i 203を13
〜30moI2%としたのは13moe%より少な(す
ると作業温度が700℃より高(なるため、コア材であ
るMn−Znフェライトに磁気特性を悪くするα−Fe
203が析出しやすくなり、しかも化学的耐久性が劣化
するためで、また30moe%より多くすると溶融、浸
透させる際に結晶化しやす(なるためである。また5i
02を30〜50mo2%としたのは、30mog%よ
り少なくするとガラスが失透しやす(耐久性が劣化する
ためで、また50moe%より多(すると作業温度が7
00℃より高くなる上に熱膨張係数が小さくなり過ぎM
n−Znフェライトの熱膨張係数と合わな(なるためで
ある。更にB2O3を1〜20moe%としたのは1m
offi%より少なくすると温度−粘度曲線の勾配が穏
やかになり作業温度が700℃より高くなるためで、2
0moe%より多くすると耐候性が劣化し且つ熱膨張係
数が小さくなり過ぎるためである。
In addition, in the above glass composition, B i 203 is 13
~30 moI2% is less than 13 moe% (then the working temperature is higher than 700°C), so the Mn-Zn ferrite core material contains α-Fe which deteriorates the magnetic properties.
This is because 203 tends to precipitate and chemical durability deteriorates, and if the amount exceeds 30 moe%, crystallization tends to occur when melting and permeating.
The reason why 02 is set to 30 to 50 mo2% is because if it is less than 30 moe%, the glass tends to devitrify (deteriorating durability), and if it is more than 50 moe%, the working temperature will be 7.
It becomes higher than 00℃ and the coefficient of thermal expansion becomes too small.
This is because it does not match the thermal expansion coefficient of n-Zn ferrite.Furthermore, B2O3 is set to 1 to 20 moe% for 1 m
This is because if it is less than offi%, the slope of the temperature-viscosity curve becomes gentle and the working temperature becomes higher than 700°C.
This is because if the amount is more than 0 moe%, the weather resistance will deteriorate and the coefficient of thermal expansion will become too small.

ところでL i 20及びNa2O,に20のうち少な
(とも1成分を含有を必須条件としたのは作業温度を低
(するためであり、特にこれらの成分が複合添加されて
いれば、いわゆる混合アルカリ効果により融点を低下さ
せると共に化学的耐久性に優れたガラスギャップを形成
することが出来るからである。
By the way, the essential condition for L i 20 and Na2O to contain one component of 20 is to lower the working temperature, and especially if these components are added in combination, the so-called mixed alkali This is because it is possible to lower the melting point and form a glass gap with excellent chemical durability.

またギャップ形成の作業温度をギャップガラス2.5 の粘度が10  ボイズから10 ポイズとなる2、5 範囲にしたのは粘度が10  ボイスより小さくなるほ
ど作業温度を高くすると、溶融ガラスがフェライト粒界
に拡散しやすくなり、逆に粘度が103ポイズより大き
くなるほど作業温度を低くするとガラスが流れに((な
り、作業性が低下し、ガラスギャップ内に気泡が残った
りするからである。
In addition, the working temperature for forming the gap was set in the range of 2.5, where the viscosity of the gap glass is 2.5 to 10 poise, from 10 to 10 poise. It becomes easier to diffuse, and conversely, if the working temperature is lowered as the viscosity becomes higher than 103 poise, the glass will flow (((), the workability will decrease, and air bubbles will remain in the glass gap.

作  用 上記のガラス組成物、作業条件によりギャップを形成す
れば、本発明の磁気ヘッドは耐環境性に優れた特性劣化
の少ないものとなる。
Function If the gap is formed using the glass composition and working conditions described above, the magnetic head of the present invention will have excellent environmental resistance and less deterioration of characteristics.

実施例 以下、本発明の実施例について説明する。Example Examples of the present invention will be described below.

まず第1図に示したごとき、所定の磁路を形成せしめる
ように切込み部2及びギャップ溝4を加工したフェライ
トブロック1にあらかじめ準備した第1表に示す組成、
特性のガラス棒3を第1図に示すごとくギャップ溝4の
上部に設置し、各ガ2.5 ラスの粘度が10  ボイズかり10 ポイズになる作
業温度で各ガラスを溶解しギャップ溝に浸透固着させた
First, as shown in FIG. 1, the composition shown in Table 1 was prepared in advance on a ferrite block 1 in which notches 2 and gap grooves 4 were processed to form a predetermined magnetic path.
As shown in Figure 1, a glass rod 3 of a specific type is installed at the top of the gap groove 4, and each glass is melted at a working temperature such that the viscosity of each glass is 10 to 10 poise, and it penetrates into the gap groove and becomes fixed. I let it happen.

(以下余白) このようにしてギャップ形成した第2図1の磁気ヘッド
部材10を鎖線5の部分より個々に切断したものを磁気
ヘッドの702827部6として、第3図に示したごと
(、別に加工したバックコア7と接着し鎖[8で示す位
置まで研摩仕上げしたものをサンプルとした。なお第1
表のガラス□のうちNo1〜No4は本発明の範囲内の
組成であり、No5.No6は比較のために準備した従
来のガラスであり、コア材としては熱膨張係数が25℃
〜300℃の温度範囲で120X10’/℃のMn−Z
nフェライトを用いた。 次に本実施例にて作製した磁
気ヘッドに於いてギャップ形成の売主じるガラスのフェ
ライトに対する拡散度を調べるために第3図に示す接着
部界面9を中心としてX線による分析を行った。
(The following is a margin) The magnetic head member 10 of FIG. 2 1 with the gap formed in this way is individually cut from the chain line 5 as the 702827 section 6 of the magnetic head, as shown in FIG. The sample was one that was bonded to the processed back core 7 and polished to the position shown by chain [8].
Among the glasses □ in the table, No. 1 to No. 4 have compositions within the scope of the present invention, and No. 5. No. 6 is a conventional glass prepared for comparison, and the core material has a thermal expansion coefficient of 25°C.
120X10'/℃ Mn-Z in the temperature range ~300℃
n-ferrite was used. Next, in order to investigate the degree of diffusion of the glass, which is responsible for forming the gap, into the ferrite in the magnetic head manufactured in this example, an X-ray analysis was performed focusing on the adhesive interface 9 shown in FIG. 3.

更にギャップ部に浸透させたガラスの化学的耐久性を調
べるために60℃−相対湿度95%雰囲気中での240
時間の耐湿試験を恒温恒湿槽を用いて行った。ここで、
耐湿試験の評価方法としては第3図に示したごとく鎖線
8の位置迄研摩して鏡面仕上げをし、触針式表面形状測
定器を用いて耐湿試験前後のガラスギャップ部近傍の表
面形状を調べた。また光学顕微鏡を用いてガラス部の変
色状況も観察した。
Furthermore, in order to investigate the chemical durability of the glass infiltrated into the gap, it was heated at 240°C in an atmosphere of 60°C and 95% relative humidity.
A humidity test for hours was conducted using a constant temperature and humidity chamber. here,
As shown in Figure 3, the evaluation method for the moisture resistance test is to polish to a mirror finish to the position indicated by chain line 8, and use a stylus type surface profile measuring device to examine the surface shape near the glass gap before and after the moisture resistance test. Ta. The state of discoloration of the glass portion was also observed using an optical microscope.

X線によるガラスのフェライトに対する拡散度の分析結
果については、本発明による磁気ヘッドのものを第5図
に、また従来例によるものを第4図に示した。
The results of X-ray analysis of the degree of diffusivity of glass with respect to ferrite are shown in FIG. 5 for the magnetic head according to the present invention, and in FIG. 4 for the conventional example.

第4図よりわかるように、高鉛含有珪酸塩ガラスのギャ
ップ部からはフェライト部に対し深さ約10μmにわた
りPbが拡散しており、その拡散部分では磁気特性が劣
化するの、みならず実効的にギャップ幅が広くなってい
る。それに対し本発明による磁気ヘッドのギャップ部か
らは第5図に示す通りほとんど拡散がみられない。また
、耐湿試験前後の表面形状について、本発明の磁気ヘッ
ドのものを第6図に、また高鉛含有珪酸塩ガラスをギャ
ップにした従来の磁気ヘッドのものを第7図に模写した
。なお、第6図(a)、第7図(a)は耐湿試験前、各
図(b)は耐湿試験後の様子を示したものである。第7
図かられかるように、高鉛含有珪酸塩ガラスの表面形状
は著しく粗くなっており、媒体との摺動の際、ノイズ、
媒体及びヘッドの損傷等の原因になるという危険性があ
る。
As can be seen from Figure 4, Pb diffuses from the gap of the high lead-containing silicate glass to a depth of approximately 10 μm into the ferrite region, and in this diffused region, not only the magnetic properties deteriorate, but also the effective The gap width is widening. On the other hand, as shown in FIG. 5, almost no diffusion is observed from the gap portion of the magnetic head according to the present invention. Furthermore, the surface shapes before and after the moisture resistance test are reproduced in FIG. 6 for the magnetic head of the present invention, and in FIG. 7 for a conventional magnetic head in which the gap is made of high lead-containing silicate glass. Note that FIGS. 6(a) and 7(a) show the state before the moisture resistance test, and each figure (b) shows the state after the humidity resistance test. 7th
As can be seen from the figure, the surface shape of high lead-containing silicate glass is extremely rough, which causes noise and noise when sliding with the medium.
There is a risk that this may cause damage to the medium and head.

また、ギャップガラスの表面は青色の干渉色を示し、い
わゆる「青やけ」現象が発生し、外観不良となった。そ
れに対し本発明の磁気ヘッドについては、第6図に示す
通り耐湿試験後のガラス表面状態は、試験前の状態に比
べてほとんど変化しておらず、ガラス表面の変色も全く
みられなかった。
Furthermore, the surface of the gap glass exhibited a blue interference color, causing a so-called "blue discoloration" phenomenon, resulting in poor appearance. On the other hand, as for the magnetic head of the present invention, as shown in FIG. 6, the glass surface condition after the moisture resistance test was almost unchanged compared to the condition before the test, and no discoloration of the glass surface was observed.

発明の効果 上述したように本発明の製造方法によって製造した磁気
ヘッドは特性劣化の少ない、信頼性の優れたものとなり
、極めて有効なるものである。
Effects of the Invention As described above, the magnetic head manufactured by the manufacturing method of the present invention has little characteristic deterioration and is highly reliable, making it extremely effective.

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

第1図、第2図、第3図は本発明の一実施例による磁気
ヘッドの製造過程を説明するための図、第4図は従来の
磁気ヘッドにおいてギャップ部からガラス成分がフェラ
イト部へ拡散した状態を示す図、第5図は本発明の一実
施例の磁気ヘッドにおいての拡散状態を示す図、第6図
は本発明のへラドギャップ部の表面形状断面図で同図(
a)は耐湿試験前断面図、同図(b)は耐湿試験前断面
図、第7図は本蚕明の実施例に対する比較例として作製
した高鉛含有珪酸塩ガラスでギヤツブ皿形成した磁気ヘ
ッドのギャップ部の表面形状断面図で同図(a)は耐湿
試験前断面図、同図(b)は耐湿試験前断面図である。 1・・・・フェライトブロック 2・・・・切り込み部    3・・・・ガラス棒4・
・・・ギャップ溝    6・・・・フロントコア部7
・・・・バックコア
Figures 1, 2, and 3 are diagrams for explaining the manufacturing process of a magnetic head according to an embodiment of the present invention, and Figure 4 shows a conventional magnetic head in which the glass component diffuses from the gap part to the ferrite part. FIG. 5 is a diagram showing the diffusion state in a magnetic head according to an embodiment of the present invention, and FIG. 6 is a cross-sectional view of the surface shape of the helad gap portion of the present invention.
a) is a cross-sectional view before the humidity test, (b) is a cross-sectional view before the humidity test, and Figure 7 is a magnetic head with a gear disk formed from high lead-containing silicate glass, which was prepared as a comparative example to the example of this Serimei. In the cross-sectional views of the surface shape of the gap portion, Figure (a) is a cross-sectional view before the moisture resistance test, and Figure (b) is a cross-sectional view before the humidity resistance test. 1... Ferrite block 2... Notch part 3... Glass rod 4.
...Gap groove 6...Front core part 7
・・・Back core

Claims (1)

【特許請求の範囲】 Bi_2O_3、SiO_2、B_2O_3の3成分を
主成分とし、且つそれぞれを Bi_2O_3:13〜30(mol%) SiO_2:30〜50(mol%) B_2O_3:1〜20(mol%) の範囲で、しかも SiO_2(mol%)+B_2O_3(mol%)>
45(mol%) SiO_2(mol%)/B_2O_3(mol%)>
2 なる関係式を満足するように含有し、残部にLi_2O
、Na_2O、K_2Oのうち少なくとも1種をそれぞ
れ Li_2O:1〜20(mol%) Na_2O:1〜18(mol%) K_2O:1〜10(mol%) の範囲内で含有してなる磁気ヘッド接合用ガラス組成物
の粘度を10^2^.^5ポイズから10^3ポイズと
なる温度範囲内で磁気ギャップ部に溶融、浸透させるこ
とを特徴とする磁気ヘッドの製造方法。
[Claims] The three main components are Bi_2O_3, SiO_2, and B_2O_3, and each of them is Bi_2O_3: 13 to 30 (mol%), SiO_2: 30 to 50 (mol%), and B_2O_3: 1 to 20 (mol%). within the range, and SiO_2 (mol%) + B_2O_3 (mol%)>
45 (mol%) SiO_2 (mol%)/B_2O_3 (mol%)>
2, and the remainder is Li_2O.
, Na_2O, and K_2O in the following ranges: Li_2O: 1 to 20 (mol%) Na_2O: 1 to 18 (mol%) K_2O: 1 to 10 (mol%). The viscosity of the glass composition is 10^2^. A method for manufacturing a magnetic head, characterized in that the magnetic head is melted and infiltrated into a magnetic gap within a temperature range of ^5 poise to 10^3 poise.
JP12965986A 1986-06-04 1986-06-04 Production of magnetic head Pending JPS62288132A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12965986A JPS62288132A (en) 1986-06-04 1986-06-04 Production of magnetic head

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12965986A JPS62288132A (en) 1986-06-04 1986-06-04 Production of magnetic head

Publications (1)

Publication Number Publication Date
JPS62288132A true JPS62288132A (en) 1987-12-15

Family

ID=15014972

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12965986A Pending JPS62288132A (en) 1986-06-04 1986-06-04 Production of magnetic head

Country Status (1)

Country Link
JP (1) JPS62288132A (en)

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