JPS6117212A - Joining of head groove part in magnetic head core - Google Patents

Joining of head groove part in magnetic head core

Info

Publication number
JPS6117212A
JPS6117212A JP13872184A JP13872184A JPS6117212A JP S6117212 A JPS6117212 A JP S6117212A JP 13872184 A JP13872184 A JP 13872184A JP 13872184 A JP13872184 A JP 13872184A JP S6117212 A JPS6117212 A JP S6117212A
Authority
JP
Japan
Prior art keywords
adhesive
silver solder
amt
alloy
components
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
JP13872184A
Other languages
Japanese (ja)
Inventor
Masanori Azuma
東 正則
Suguru Motonishi
本西 英
Takamichi Ito
伊藤 孝道
Akifumi Kanbe
神戸 章史
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.)
Kobe Steel Ltd
Original Assignee
Kobe Steel 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 Kobe Steel Ltd filed Critical Kobe Steel Ltd
Priority to JP13872184A priority Critical patent/JPS6117212A/en
Publication of JPS6117212A publication Critical patent/JPS6117212A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/127Structure or manufacture of heads, e.g. inductive
    • G11B5/1272Assembling or shaping of elements

Landscapes

  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)

Abstract

PURPOSE:To obtain adequate hardness and to make the wear resistance of an adhesive agent equal to the wear resistance of a base metal by forming an adequate amt. of oxide in the adhesive agent. CONSTITUTION:The silver solder adhesive agnet prepd. by compounding alloy components of 1 or >=2 kinds selected from Mn, In, Sn, and Sb as the substitution type components with Ag-Cu-Zn-Cd silver solder in a manner as to satisfy a 1-10wt% range on the entire compsn. of the ashesive agent is embedded in a cavity part and is heated in a non-oxidative atmosphere to braze the cavity part. The brazed part is thereafter heated to 350-600 deg.C in an oxidative amt. to oxidize partly the silver solder components. The adequate range exists in the amt. of the solute elements to be compounded. The effect of improving the wear resistance is weakened at <1% and the deposited state of the oxide is made defective and the improving effect is unstable when the amt. exceeds 10%. The oxidation of the solute elements is not enough if the heating temp. is below 350 deg.C and the base components (solvent alloy) of the Ag-Cu-Zn-Cd alloy soften and the elements constituting the adhesive agent diffuse into the base metal when said temp. exceeds 600 deg.C. The deterioration in the recording and reproducing characteristics and further defective adhesion are then resulted.

Description

【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コアの製造工程における接着工程の
改良に関し、詳細には磁気ヘッドコアのヘッド部におけ
る母材部分と接着剤部分の摩耗挙動を可及的均一化する
ことのできる改良製造方法に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an improvement in the adhesion process in the manufacturing process of a magnetic head core, and more specifically, to improving the abrasion behavior of the base material portion and the adhesive portion in the head portion of the magnetic head core. This invention relates to an improved manufacturing method that can achieve uniformity.

[従来の技術] ビデオ用或は音声用の磁気記録媒体に関しては情報信号
を狭トラツク内へ高密度に記録したいという要望が強い
、この要望に応えるものとして、センダスト系合金を用
いたものが開発されつつあり、狭ギヤツプ幅且つ狭トラ
ツク幅の磁気ヘッドコアが提供される様になってきてい
る。センダスト系合金で代表される金属磁性材料は、従
来のフェライト系材料に比べて飽和磁束密度が高いとい
う特性がありその面で注目されているが、フェライト系
材料において確立されている製造手法はそのまま金属磁
性材料製ヘッドの製造に転用できない面があり、例えば
ブロック板の固着用として新たに銀ろうを用いる方法等
が開発されている。
[Prior Art] There is a strong desire to record information signals in a narrow track with high density in magnetic recording media for video or audio.In order to meet this demand, a medium using sendust alloy was developed. As a result, magnetic head cores with narrow gap widths and narrow track widths are being provided. Metallic magnetic materials such as sendust alloys have a characteristic of having a higher saturation magnetic flux density than conventional ferrite-based materials, and are attracting attention for this reason, but the manufacturing method established for ferrite-based materials remains unchanged. There are some aspects that cannot be applied to the production of heads made of metal magnetic materials, and for example, new methods have been developed that use silver solder for fixing block plates.

第4図はセンダスト系合金(以下本明細書では単にセン
ダストという)を材料とする従来の製造手順を示す説明
図である。まず(A)工程ではセンダストの矩形ブロッ
ク1からブロック板2を切出す。次に(、B)工程(一
般にウェハ加工と称している)では、ブロック板を溝加
工用ブロック板2aと非溝加工用ブロック板2bに分け
、前者2aの板面(特に片側面)に直線溝3を形成する
。直線溝3は後述のコイル巻回窓W[第4図(H)参照
]を形成する為のものであり、溝加工用ブロック板2a
の片側に寄せると共に側縁Sと平行に形成するのが一般
的である。そして直線溝3を挟んで狭い方の堤をフロン
ト部4と称し、広い方の堤をバック部5と称している。
FIG. 4 is an explanatory diagram showing a conventional manufacturing procedure using a Sendust alloy (hereinafter simply referred to as Sendust in this specification) as a material. First, in step (A), a block plate 2 is cut out from a rectangular block 1 of sendust. Next, in step (B) (generally referred to as wafer processing), the block plate is divided into a groove processing block plate 2a and a non-groove processing block plate 2b, and a straight line is formed on the plate surface (especially one side surface) of the former 2a. A groove 3 is formed. The straight groove 3 is for forming a coil winding window W (see FIG. 4(H)), which will be described later, and is used as a groove machining block plate 2a.
It is common to form it parallel to the side edge S and to one side of the side edge S. The narrower bank with the straight groove 3 in between is called the front part 4, and the wider bank is called the back part 5.

っぎの(C)工程ではフロント部4の表面に非接着性加
工(磁性をもたない物質を薄膜状に被着させる工程であ
り、非磁性膜被着加工ともいう)4aを施し、非溝加工
用ブロック板2bには、フロント部4bと対面[第4図
(E)参照]する面に、直線溝3と直交する方向のくし
削り加工を施して狭いトラックIll!Tのくし刃6を
形成する。そして(D)工程では、前出のトラック幅T
が完全に一致する様なくし刃7をフロント部4に形成す
る。
In step (C), the surface of the front part 4 is subjected to non-adhesive processing (a process in which a non-magnetic substance is applied in a thin film form, also referred to as non-magnetic film adhesion processing) 4a, and a non-grooved The surface of the processing block plate 2b facing the front portion 4b [see FIG. 4(E)] is comb-cut in a direction perpendicular to the straight groove 3 to create a narrow track Ill! A T-shaped comb blade 6 is formed. In step (D), the track width T
A comb blade 7 is formed on the front part 4 so that the comb blades 7 are completely matched with each other.

これらのくし刃6,7で挟まれる四部を本明細書ではヘ
ッド溝9.lOと称することとする。
In this specification, the four parts sandwiched between these comb blades 6 and 7 are referred to as head grooves 9. It will be referred to as lO.

次に(E)工程では、2枚のブロック板2a。Next, in step (E), two block plates 2a are formed.

2bを向き合わせる様に積層し、両者を接合する。接合
に当たっては、バック部5の表面と、これに対向するブ
ロック2bの表面との間に銀ろう等を介在させているが
、フロント部4については前述の如き非接着性加工(例
えばシリカ蒸着膜の形成)を行な゛っているので、゛バ
ック部5のみが接合され、フロント部4は対向当接して
いるだけである。尚本(E)工程では、ヘッド溝9,1
0が対向することによって腔部11が形成される。そし
て(F)工程ではこの腔部11に接着剤8が埋込まれ、
くし刃6,7の当接面を両脇から補強する。更に(’G
)工程では切断分割[切断線は(F)工程を示す図に破
線で示しており、角度αのごとをアジマス角度と称して
いるゴが行なわれ、最後に(H)工程ではフロント部4
側の頂面が球面状に研摩さ・れ磁気へ一2ドコア12が
製造される。
2b are stacked so as to face each other, and both are joined. For joining, silver solder or the like is interposed between the surface of the back part 5 and the surface of the block 2b facing it, but the front part 4 is treated with non-adhesive treatment as described above (for example, a silica vapor deposited film). Since only the back part 5 is joined and the front part 4 is in opposing contact with each other. In the main (E) process, head grooves 9, 1
A cavity 11 is formed by the two facing each other. Then, in step (F), adhesive 8 is embedded in this cavity 11,
The contact surfaces of the comb blades 6 and 7 are reinforced from both sides. Furthermore ('G
) process, cutting and dividing [the cutting line is shown as a broken line in the diagram showing the (F) process, and each angle α is called an azimuth angle is performed, and finally, in the (H) process, the front part 4
The top surface of the side is polished into a spherical shape to produce a magnetic core 12.

ところで第5図は磁気ヘッドコアの平面図、第6図は第
5図におけるVI−Vl線断面拡大図を示すが、第5図
はテープの摺動面(テープの走行方向は矢印X)を表わ
し、第6図では紙面貫通方向にテープが走行する。そし
てテープとの摺動摩耗状況が第6図に表われており、く
し刃6は母材(センダスト)で構成され高硬度である故
に摩耗量が極めて少ないのに対し、接着剤8は銀ろうで
構成され低硬度である故に摩耗量が極めて多゛い。その
為第6図に示す如き偏摩−(深゛さD)が発生し磁気ヘ
ッドコアの出力特性に重大な影響力を現われる。
Incidentally, FIG. 5 shows a plan view of the magnetic head core, and FIG. 6 shows an enlarged cross-sectional view taken along the line VI-Vl in FIG. , in FIG. 6, the tape runs in the direction penetrating the page. Figure 6 shows the state of wear due to sliding with the tape.The comb blade 6 is made of base material (sendust) and has high hardness, so the amount of wear is extremely small, while the adhesive 8 has silver solder. The amount of wear is extremely high due to its low hardness. As a result, polarization (depth D) as shown in FIG. 6 occurs, which has a significant influence on the output characteristics of the magnetic head core.

[発明が解決しようとする問題点] 従来の磁気ヘッドコアでは、テープとの摺動面を構成す
る母材と接着剤が強度面において顕著な差を有している
為、テープとの摩擦にょる゛上′記の”偏摩耗が比較的
短時間のうちに現われ、しかもその深さDもかなり大き
いものになる。従って接着剤として高硬度のものを選び
さえすれば上記偏摩耗もかなり抑制できるはずであると
考えられたが、もとより接着強度や埋込作業性を低下さ
せるものであってはならず、これらの条件を全て満足で
きる接着剤の開発が当面の課題となる。本発明はこの様
な状況に鑑みてなされたものであるが、特殊組成の銀ろ
うを用い、且つ特殊処理を施すことによって前記の全条
件が満足されることを見出し本発明を完成するに至った
[Problems to be Solved by the Invention] In conventional magnetic head cores, there is a significant difference in strength between the base material and the adhesive that make up the sliding surface with the tape. ``The uneven wear described above appears in a relatively short period of time, and its depth D is also quite large.Therefore, as long as an adhesive with high hardness is selected, the uneven wear described above can be significantly suppressed. However, the current challenge is to develop an adhesive that satisfies all of these conditions, as it must not reduce adhesive strength or embedding workability. This invention was developed in view of the above circumstances, and the present invention was completed by discovering that all of the above conditions could be satisfied by using a silver solder with a special composition and by subjecting it to a special treatment.

[問題点を解決する為の手段] 接着強度や埋込作業性に悪影響を与えずに母材に匹敵し
得る耐摩耗性を発揮する接着剤埋込部は、次に示す手段
に′よって形成することができた。即ち本発明は、ヘッ
ド溝加工の施されたブロック板を対面させ対向するヘッ
ド溝によって構成される腔部に接着剤を埋込んでヘッド
溝部の接合を行なうに当たり、AjH,Cu、Zn及び
Cdを基本成分とするA g −Cu−Z n −Cd
基鈑ろうに、M n 、 I n 、 S n及びSb
から選択される1種又は2種以上の合金成分を、全接着
剤組成中の1〜10重量%(以下単に%)の範囲を満足
する様に置換型成分として配合してなる銀ろう系接着剤
を前記腔部に埋込み、非酸化性雰囲気下に加熱してろう
行処理した後、酸化性雰囲気下における350〜600
℃の加熱によって銀ろう成分の一部を酸化する工程を含
む点に要旨を有するものである。
[Means for solving the problem] An adhesive embedded part that exhibits abrasion resistance comparable to the base material without adversely affecting adhesive strength or embedding workability can be formed by the following method. We were able to. That is, in the present invention, AjH, Cu, Zn, and Cd are used to bond the head grooves by embedding an adhesive in the cavity formed by the opposing head grooves by placing the block plates with the head grooves facing each other. A g -Cu-Z n -Cd as the basic component
Rouni Kikan, M n , I n , S n and Sb
A silver solder adhesive comprising one or more alloy components selected from the following as substitutional components in an amount of 1 to 10% by weight (hereinafter simply referred to as %) of the total adhesive composition. The agent is embedded in the cavity, heated in a non-oxidizing atmosphere and waxed, and then heated to 350 to 600 in an oxidizing atmosphere.
The gist of this method is that it includes a step of oxidizing a part of the silver solder component by heating at .degree.

[作用] ヘッド溝の対向によって構成される腔部への埋込用接着
剤(以下単に接着剤という)を改善し得た点に本発明の
基本的な特性がある。従ってこの接着剤について説明す
ると、ベースとしてはAg 、Cu 、Zn及びCdを
含むAg−Cu−Zn−Cd系銀ろうを採用し、これに
以下述べる様な溶質元素を置換型元素として配合すると
共に接着工程の条件を工夫することによって接着剤部分
の耐摩耗性を向上せしめているものである。
[Operation] The basic characteristic of the present invention is that the adhesive for embedding into the cavity formed by the opposing head grooves (hereinafter simply referred to as adhesive) can be improved. Therefore, to explain this adhesive, Ag-Cu-Zn-Cd silver solder containing Ag, Cu, Zn, and Cd is used as the base, and solute elements as described below are blended as substitutional elements. The abrasion resistance of the adhesive part is improved by adjusting the conditions of the bonding process.

まず基本組成であるAg−Cu−Zn−Cd系銀ろうに
ついては、ろう材としての特性を発揮し得るものである
限り組成面において特段の制限を受ける訳ではない。但
しもっとも代表的且つ汎用的であるのはJIS銀ろうの
BAg−1゜BAg−IA、BAg−2である。そして
これらの合金組成は第1表に示す通りである。
First, the basic composition of the Ag-Cu-Zn-Cd based silver solder is not particularly limited in terms of composition as long as it can exhibit the properties as a brazing material. However, the most typical and widely used are JIS silver solder BAg-1°BAg-IA and BAg-2. The compositions of these alloys are shown in Table 1.

第   1   表 (%) 従って本発明のAg−Cu−Zn−Cd系銀ろうにおけ
るAg、Cu、Zn、Cdの各含有量は、上記第1表を
参酌して定めればよいが、以下の説明においては、BA
g−1の銀ろうを基本組成とする場合を代表的に取上げ
て述べるものとする。即ちBAg−1の成分組成は、A
g:44〜46%、Cu:14〜16%、Zn:14〜
18%、Cd:2.3〜25%であるから、AgO,4
5°u0.152”0.16 cdo、24を平均組成
とし、これをもって以下Ag−Cu−Zn−Cd系銀ろ
うを代表的に意味せしめるものとする。
Table 1 (%) Therefore, the content of each of Ag, Cu, Zn, and Cd in the Ag-Cu-Zn-Cd silver solder of the present invention may be determined with reference to Table 1 above. In the explanation, BA
The case where the basic composition is silver solder g-1 will be described as a representative example. That is, the component composition of BAg-1 is A
g:44~46%, Cu:14~16%, Zn:14~
18%, Cd: 2.3-25%, so AgO,4
The average composition is 5° u0.152" 0.16 cdo, 24, which will hereinafter be representatively used to mean Ag-Cu-Zn-Cd based silver solder.

本発明の接着剤は、前述の如く溶質元素を置換的に配合
したものであり、溶質元素をY、配合率がX%であると
すれば次の様に表現することができる。
The adhesive of the present invention is one in which solute elements are substituted as described above, and if the solute element is Y and the blending ratio is X%, it can be expressed as follows.

(Ag O,45Cu0.15ZnO,16cd0.2
4〕(100−x)/] 0OYx/100溶質元素Y
としては、Mn、In、Sn、Sbが例示され、これら
の中から1種又は2種以上選択して配合される。溶質元
素Yの配合は、ろう付後の酸化処理によって溶質元素を
高硬度の酸化物に変換し、それによって接着剤の耐摩耗
性を母材のそれに匹敵し得る程度まで向上するものであ
る。従って溶質元素Yの配合量(溶質元素Yが2種以上
であるときはそれらの給配合量)については適正な範囲
が存在し、1%未満では溶質元素の酸化物生成量も少な
い為耐摩耗性の向上効果は弱くなる。従って1%以上の
配合が必要となるが、酸化物の生成による耐摩耗性の改
善効果が安定して発揮されるのは10%までであり、1
0%を超えると酸化物の析出状態が不良となって改善効
果が不安定になってくる。
(Ag O, 45Cu0.15ZnO, 16cd0.2
4〕(100-x)/] 0OYx/100 solute element Y
Examples include Mn, In, Sn, and Sb, and one or more of these may be selected and blended. The solute element Y is blended to convert the solute element into a highly hard oxide through oxidation treatment after brazing, thereby improving the wear resistance of the adhesive to a level comparable to that of the base material. Therefore, there is an appropriate range for the blending amount of solute element Y (if there are two or more types of solute element Y, their blending amounts), and if it is less than 1%, the amount of solute element oxide produced is small, so it is resistant to wear. The effect of improving sex becomes weaker. Therefore, a content of 1% or more is required, but the effect of improving wear resistance due to the production of oxides is stably exhibited at up to 10%.
If it exceeds 0%, the precipitation state of the oxide becomes poor and the improvement effect becomes unstable.

上記組成からなる接着剤は、第4図の(F)工程におい
て腔部へ充填されるが、ここでは(A)のろう付処理の
工程CB)の酸化の工程が行なわれる。(A)のろう付
処理は標準のろう付条件に従って行なうが、重要な点は
非酸化性に富んだ溶質元素がこの段階で過度に酸化され
て複雑な酸化物を形成し接着力の発揮に対して不都合な
悪影響を生ぜしめない様にすることであり、その為には
ろう付処理を非酸化性雰囲気(例えば真空或は不活性ガ
ス雰囲気)にすることが要求される。この様な条件であ
れば接着剤の酸化のみならず母材となるセンダストの酸
化も防止され良質の磁気ヘッドコアが得られる。ろう付
の為の温度は、当然に溶融点以上でなければならない。
The adhesive having the above composition is filled into the cavity in step (F) of FIG. 4, where the oxidation step of step CB) of the brazing treatment of (A) is performed. The brazing process (A) is carried out according to standard brazing conditions, but the important point is that the solute elements, which are rich in non-oxidizing properties, are excessively oxidized at this stage and form complex oxides, which inhibit the performance of adhesive strength. The objective is to prevent any undesirable adverse effects from occurring, and for this purpose, it is required that the brazing process be performed in a non-oxidizing atmosphere (for example, a vacuum or an inert gas atmosphere). Under these conditions, not only the oxidation of the adhesive but also the oxidation of the sendust, which is the base material, is prevented, and a magnetic head core of good quality can be obtained. The temperature for brazing must naturally be above the melting point.

但し750℃を超えると接着剤を構成する元素が母材中
に拡散してセンダストの合金組成に変化を与え、磁気ヘ
ッドの記録再生特性が悪化するという問題が生じる。更
に接着不良も招く。尚加熱時間は5分以上として完全に
溶融し母材との濡れを促進することが望ましい。加熱時
間が長くなるほど濡れが良くなって接着効果は光道して
いくが、この冗進は2時間程度で飽和に達すると共に加
熱温度が高い場合と同様合金成分の拡散が見られるので
、2時間をもって上限とすべきである。尚非酸化性雰囲
気の形成について特に真空下でのろう付を行なう場合は
10− ’ torr以下の真空度にしなければ前記濡
れ性ガスが不十°分となって接着不良を招くことがある
ので注意を要する。
However, if the temperature exceeds 750° C., the elements constituting the adhesive will diffuse into the base material, changing the alloy composition of the sendust, causing a problem that the recording and reproducing characteristics of the magnetic head will deteriorate. Furthermore, it also causes poor adhesion. It is preferable that the heating time be 5 minutes or longer to completely melt and promote wetting with the base material. The longer the heating time, the better the wetting becomes and the better the adhesion effect becomes. However, this overgrowth reaches saturation in about 2 hours, and diffusion of alloy components is observed as in the case of high heating temperatures, so The upper limit should be . Regarding the formation of a non-oxidizing atmosphere, especially when performing brazing under vacuum, the degree of vacuum must be maintained at 10-' torr or less, otherwise the wetting gas may not be present sufficiently, resulting in poor adhesion. Caution is required.

(A)のろう付が完了すると(B)の酸化工程に入るが
ろう付温度の降下途中で酸化を行なうのが熱経済的に見
てもつとも有利である。酸化工程は当然に酸化性雰囲気
で行なう必要があり、この時の雰囲気中における酸素含
宥量は5〜40容量%の範囲を満足することが推奨され
、残りの気体としては窒素やアルゴン等の不活性ガス力
(望まれる。酸化工程における加熱温度としては、35
0〜600℃の範囲から選択する必要があり、350℃
未満では溶質元素の酸化が不十分となる。しかし600
℃を超えるとAg−Cu−Zn−Cd系合金の毒成分(
溶媒合金)が軟化しはじめ、(A)のろう付温度が高温
になり過ぎたのと同様の欠陥が生じてくる。加熱時間は
lO分〜2時間が好ましく、10分未満では溶質元素の
酸化が不十分なままで終ることがある。他方上限につい
ては、酸化反応が2時間以゛内に十分完了するどころか
ら上記の範囲を推奨することとした。尚3時間を超える
と表面の酸化が過度に進行し、着色によって商品価値を
低下させることがある。
When the brazing (A) is completed, the oxidation step (B) begins, and it is advantageous from a thermoeconomic standpoint to carry out the oxidation while the brazing temperature is decreasing. The oxidation process naturally needs to be carried out in an oxidizing atmosphere, and it is recommended that the oxygen content in the atmosphere at this time be in the range of 5 to 40% by volume, with the remaining gas being nitrogen, argon, etc. Inert gas power (desired. Heating temperature in the oxidation step is 35
Must be selected from the range of 0 to 600℃, 350℃
If it is less than that, the oxidation of the solute element will be insufficient. But 600
If the temperature exceeds ℃, the poisonous components of Ag-Cu-Zn-Cd alloy (
Solvent alloy) begins to soften, and defects similar to those caused when the brazing temperature in (A) becomes too high occur. The heating time is preferably 10 minutes to 2 hours; if it is less than 10 minutes, the oxidation of the solute element may be insufficient. On the other hand, regarding the upper limit, the above range is recommended because the oxidation reaction is sufficiently completed within 2 hours. If the time exceeds 3 hours, oxidation of the surface may progress excessively, resulting in coloration and a decrease in commercial value.

以上で本発明における必須の構成を説明し且つ好適範囲
を述べることによって本発明の作用を明らかにしたが、
本発明の接着剤を適用するための磁気ヘッドコア製造工
程は前第4図に示したものに限定されず、本発明者等の
出願に係る特願昭59−98398においそ提案した改
良製造工程或はその他種々検討されている製造工程にお
ける接着剤の埋込みには全て適用することが可能である
The operation of the present invention has been clarified above by explaining the essential configurations of the present invention and stating the preferred range.
The magnetic head core manufacturing process to which the adhesive of the present invention is applied is not limited to that shown in FIG. This method can be applied to all other methods of embedding adhesives in manufacturing processes that have been considered.

[実施例] 〔Ago、45cuO,15ZnO,16cd0.24
−’ o、960.04(但しYはMn、In、Sn、
Sbから選択される1種又は2種以上の溶質元素を意味
する)で示される接着剤(粒状合金)を、第4図(F)
工程において腔部11に埋込んだ。まずl O−’ t
orr以下の真空中で700℃X30分のろう付処理を
行ない、次にこれを冷却する途中500℃X30分(空
気中)の酸化処理を行なった。これにより接着剤と母材
を強固に接合させると共に、接着剤中に溶質元素の微細
酸化物を析出させた。第4図の全工程を遂行して得られ
た磁気ヘッドコアを用い、塗布型メタルテープの走行テ
ストを行なったところ、第1図に示す様な結果が得られ
た。尚第1図には酸化工程を経なかったもの(φ印)に
ついて、これを比較例として掲げた。
[Example] [Ago, 45cuO, 15ZnO, 16cd0.24
-' o, 960.04 (However, Y is Mn, In, Sn,
An adhesive (granular alloy) represented by one or more solute elements selected from Sb is shown in FIG. 4 (F).
It was embedded in the cavity 11 during the process. First l O-' t
Brazing treatment was performed at 700° C. for 30 minutes in a vacuum of orr or less, and then, during cooling, oxidation treatment was performed at 500° C. for 30 minutes (in air). As a result, the adhesive and the base material were firmly bonded, and fine oxides of solute elements were precipitated in the adhesive. When a coated metal tape running test was conducted using the magnetic head core obtained by performing all the steps shown in FIG. 4, the results shown in FIG. 1 were obtained. In addition, in FIG. 1, a product that did not undergo the oxidation process (marked with φ) is shown as a comparative example.

(テープの走行テスト条件) 保磁力Hc:1450エルステツド、ai重密度145
 emu/gの鉄粉が塗布されたテープを使用。
(Tape running test conditions) Coercive force Hc: 1450 oersted, ai density 145
Use tape coated with emu/g iron powder.

市販のビデオデツキ(1/2インチ、VH3方式)を使
用し、40±2℃、RH70%の下で1000時間の走
行を行なった。
A commercially available video deck (1/2 inch, VH3 system) was used and run for 1000 hours at 40±2° C. and RH 70%.

第1図に見られる如く、溶質元素の添加をしなかったも
のでは酸化処理の有無に拘わらず2.5〜3pmの偏摩
耗が見られたのに対し、溶質元素を添加し且つ酸化処理
を行なったものでは偏摩耗量がlpm以下であり、接着
剤部分の耐摩耗性が顕著に改善された跡をうかがうこと
ができる。尚溶質元素を加えないで酸化処理を行なった
一例では、本発明例はどの効果は示していないが、溶質
元素無添加・酸化処理なしの例に比べて偏摩耗量がかな
り少なくなっている。これは溶媒元素中のZnやCdの
一部が酸化されて析出し、これが接着剤に多少の高硬度
を与えて耐摩耗性の向上に若干寄与した為であろうと考
えている。
As seen in Figure 1, uneven wear of 2.5 to 3 pm was observed in the case without solute elements added regardless of whether or not oxidation treatment was performed, whereas in the case of the case in which solute elements were added and oxidation treatment was performed. In the case of the adhesive, the amount of uneven wear was less than 1pm, and it can be seen that the wear resistance of the adhesive portion was significantly improved. In an example in which oxidation treatment was performed without adding a solute element, the example of the present invention did not show any effect, but the amount of uneven wear was considerably smaller than in an example in which no solute element was added and no oxidation treatment was performed. It is believed that this is because some of the Zn and Cd in the solvent elements were oxidized and precipitated, which gave the adhesive some high hardness and slightly contributed to improving the wear resistance.

次に溶質元素の種類及び配合量を少しずつ変化させなが
ら、他の条件は第1図の場合と同じにして走行テ゛スト
を行なった。結果は第2図に示す通りであって、溶質元
素の添加が1%未満のもの(図では0%)、10%・を
超えるもの(図では15%)については偏摩耗が多かっ
た。即ち0%のものでは接着剤が軟質であった為偏摩耗
が起こり易く、15%のものでは酸化物が多過ぎる為こ
れらが走行テープの摺擦圧によって剥離し却って偏摩耗
を招く様であった。
Next, a running test was conducted while changing the type and amount of the solute element little by little while keeping the other conditions the same as in the case of FIG. 1. The results are as shown in FIG. 2, and uneven wear was common in cases where the solute element addition was less than 1% (0% in the figure) and in cases where it exceeded 10% (15% in the figure). In other words, with 0% adhesive, the adhesive was soft and uneven wear was likely to occur, while with 15% adhesive, there were too many oxides, so these were likely to peel off due to the sliding pressure of the running tape, causing uneven wear. Ta.

次に溶質元素の添加量を0%又は4%とし、酸化工程に
おける加熱温度を種々変化(加熱時間は30分)して同
様のテストを行なった。第3図は。
Next, similar tests were conducted with the solute element added at 0% or 4% and the heating temperature in the oxidation step varied (heating time was 30 minutes). Figure 3 is.

その結果を示すものであって、350℃未満(図中の5
0℃と300℃)では溶質元素の酸化が進まなかったの
で偏摩耗が大きく、750℃超(図中の600℃)では
溶質元素の酸化物が粗大化され、又溶媒元素であるAg
やCuの酸化も進む為、却って接着剤がもろくなり偏摩
耗が発生した。
This shows the results below 350℃ (5 in the figure).
At temperatures above 750°C (600°C in the figure), the oxides of the solute elements become coarse and the solvent element Ag
As the oxidation of Cu and Cu progressed, the adhesive became brittle and uneven wear occurred.

[発明の効果] 本発明は上記の如く構成されているので、接着剤中に適
量の酸化物を形成することによって適度の硬度が与えら
れ、その結果接着剤の耐摩耗性が母材差みとなった。従
って磁気ディスクコアとして長時間使用した場合であっ
ても接着剤部分の偏摩耗が少なくなり、良好な記録再生
特性を長時間に亘って発揮することが可能となった。
[Effects of the Invention] Since the present invention is configured as described above, appropriate hardness is imparted by forming an appropriate amount of oxide in the adhesive, and as a result, the wear resistance of the adhesive is improved depending on the base material. It became. Therefore, even when used as a magnetic disk core for a long time, uneven wear of the adhesive portion is reduced, making it possible to exhibit good recording and reproducing characteristics over a long period of time.

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

第1〜3図は偏摩耗深さに及ぼす各要因の影響度を示す
グラブ、第4図は磁気ヘッドコアの製造工程を示す説明
図、第5図は磁気ヘッドコアの平面図、第6図は第5図
におけるVl−VI線断面拡大図である。
Figures 1 to 3 are graphs showing the degree of influence of each factor on uneven wear depth, Figure 4 is an explanatory diagram showing the manufacturing process of the magnetic head core, Figure 5 is a plan view of the magnetic head core, and Figure 6 is a graph showing the influence of each factor on uneven wear depth. 5 is an enlarged cross-sectional view taken along the line Vl-VI in FIG. 5. FIG.

Claims (1)

【特許請求の範囲】[Claims] ヘッド溝加工の施されたブロック板を対面させ対向する
ヘッド溝によって構成される腔部に接着剤を埋込んでヘ
ッド溝部の接合を行なう方法において、Ag、Cu、Z
n及びCdを基本成分とするAg−Cu−Zn−Cd系
銀ろうに、Mn、In、Sn及びSbから選択される1
種以上又は2種以上の合金成分を、全接着剤組成中の1
〜10重量%の範囲を満足する様に置換型成分として配
合してなる銀ろう系接着剤を前記腔部に埋込み、非酸化
性雰囲気下に加熱してろう付処理した後、酸化性雰囲気
下における350〜600℃の加熱によって銀ろう合金
成分の一部を酸化する工程を含むことを特徴とする磁気
ヘッドコアの製造におけるヘッド溝部の接合方法。
Ag, Cu, Z
1 selected from Mn, In, Sn and Sb to Ag-Cu-Zn-Cd based silver solder having n and Cd as basic components.
One or more types or two or more types of alloy components in the total adhesive composition.
A silver solder adhesive compounded as a substituted component to satisfy the range of ~10% by weight is embedded in the cavity, heated and brazed in a non-oxidizing atmosphere, and then soldered in an oxidizing atmosphere. A method for joining a head groove in manufacturing a magnetic head core, the method comprising the step of oxidizing a part of a silver solder alloy component by heating at 350 to 600°C.
JP13872184A 1984-07-03 1984-07-03 Joining of head groove part in magnetic head core Pending JPS6117212A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13872184A JPS6117212A (en) 1984-07-03 1984-07-03 Joining of head groove part in magnetic head core

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13872184A JPS6117212A (en) 1984-07-03 1984-07-03 Joining of head groove part in magnetic head core

Publications (1)

Publication Number Publication Date
JPS6117212A true JPS6117212A (en) 1986-01-25

Family

ID=15228587

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13872184A Pending JPS6117212A (en) 1984-07-03 1984-07-03 Joining of head groove part in magnetic head core

Country Status (1)

Country Link
JP (1) JPS6117212A (en)

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