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JPH0580044B2 - - Google Patents
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JPH0580044B2 - - Google Patents

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Publication number
JPH0580044B2
JPH0580044B2 JP60032089A JP3208985A JPH0580044B2 JP H0580044 B2 JPH0580044 B2 JP H0580044B2 JP 60032089 A JP60032089 A JP 60032089A JP 3208985 A JP3208985 A JP 3208985A JP H0580044 B2 JPH0580044 B2 JP H0580044B2
Authority
JP
Japan
Prior art keywords
substrate
magnetic
thermal expansion
nio
magnetic head
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
JP60032089A
Other languages
Japanese (ja)
Other versions
JPS61192005A (en
Inventor
Osamu Inoe
Takeshi Hirota
Toshihiro Mihara
Mitsuo Satomi
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 JP60032089A priority Critical patent/JPS61192005A/en
Publication of JPS61192005A publication Critical patent/JPS61192005A/en
Publication of JPH0580044B2 publication Critical patent/JPH0580044B2/ja
Granted legal-status Critical Current

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  • Magnetic Heads (AREA)
  • Thin Magnetic Films (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、磁気ヘツドの構成の改良に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to an improvement in the construction of a magnetic head.

従来の技術 従来、磁気ヘツドの構成として、磁気コア材料
に、軟磁性のパーマロイ・センダスト・アモルフ
アス合金・Mn−Zn−フエライト等を使用し、こ
れを基板に接合又は接着するか、基板上に蒸着・
スパツタ・CVD・メツキ等の方法で形成したも
のが用いられてきた。
Conventional technology Conventionally, magnetic heads have been constructed by using soft magnetic permalloy, sendust, amorphous alloy, Mn-Zn-ferrite, etc. as the magnetic core material, and bonding or adhering this to a substrate, or depositing it on the substrate.・
Materials formed by sputtering, CVD, plating, etc. have been used.

このような構成の磁気ヘツドでは、軟磁性材料
と基板材料の熱膨張係数が等しいか、又はその差
が極めて小さくなければ、温度変化によつて両材
料の界面に応力が生じ、亀裂発生の原因となつた
り、あるいは磁歪効果によつて軟磁性材料の磁気
特性が悪化する。このため、使用する軟磁性材料
の種類・組成による熱膨張係数に対応して、自由
に熱膨張係数を変える事のできる基板材料が必要
となり、結晶化ガラス,CaO−SrO−TiO2系セ
ラミツク基板(特開昭52−57218号公報)、
NiMnO2系セラミツク基板(特開昭53−16399号
公報)などが使用されていた。これらの基板材料
は、その組成を調整する事により、広い範囲で熱
膨張係数を選択できるものである。
In a magnetic head with such a configuration, unless the soft magnetic material and the substrate material have the same coefficient of thermal expansion, or the difference between them is extremely small, stress will be generated at the interface between the two materials due to temperature changes, causing cracks. or the magnetic properties of the soft magnetic material deteriorate due to the magnetostrictive effect. For this reason, a substrate material whose thermal expansion coefficient can be freely changed according to the type and composition of the soft magnetic material used is required, such as crystallized glass, CaO-SrO- TiO2 ceramic substrates (Japanese Unexamined Patent Publication No. 52-57218),
NiMnO 2 ceramic substrates (Japanese Unexamined Patent Publication No. 16399/1983) were used. The coefficient of thermal expansion of these substrate materials can be selected from a wide range by adjusting the composition.

発明が解決しょうとする問題点 しかしながら、結晶化ガラスやCaO−SrO−
TiO2系基板では、成分としてアルカリ金属、あ
るいはCaを含むために使用時の環境条件、特に
湿度変化に対して化学的に不安定であり、これら
の基板を用いて磁気ヘツドを構成した場合、耐
候・耐久性に関して問題を生じていた。一方、
NiMnO2系基板を用いた場合では、温度変化に対
する問題はないと考えられるが、MnOが空気中
で加熱されると酸化されてMn2O3になりやすい
ために、熱的安定性が充分でなく、また基板自体
に関して、焼成雰囲気を非酸化性にしなければな
らないために製造コストが高くなり、さらにNiO
とMnOの格子定数の差が大きいために固溶体が
形成されにくく、焼結性が悪いなどの欠点があつ
た。
Problems to be solved by the invention However, crystallized glass and CaO−SrO−
Since TiO 2 -based substrates contain alkali metals or Ca as components, they are chemically unstable against environmental conditions during use, especially changes in humidity, and when a magnetic head is constructed using these substrates, There were problems with weather resistance and durability. on the other hand,
When using a NiMnO 2 -based substrate, there is no problem with temperature changes, but since MnO is easily oxidized to Mn 2 O 3 when heated in air, it may not have sufficient thermal stability. In addition, the manufacturing cost is high because the firing atmosphere must be non-oxidizing for the substrate itself, and NiO
Due to the large difference in lattice constant between MnO and MnO, it is difficult to form a solid solution, resulting in poor sinterability.

問題点を解決するための手段 本発明は前問題点を解決するために、岩塩型結
晶構造を持ち、複合酸化物MgxNi1-xO(0<x<
1)を主成分とする基板を用い、この基板上に磁
気コアとして軟磁性材料を形成した事を特徴とす
る磁気ヘツドである。
Means for Solving the Problems In order to solve the previous problems, the present invention has a rock salt type crystal structure and a complex oxide Mg x Ni 1-x O (0<x<
This magnetic head is characterized in that it uses a substrate containing 1) as a main component, and a soft magnetic material is formed as a magnetic core on this substrate.

作 用 発明者等は研究の結果、耐湿・耐熱性に優れた
NiOにMgOを固溶させる事により、熱膨張係数
を100〜140×10-7/℃の範囲内で調節可能な事を
見い出した。MgOは水に対して溶解性を持ち、
耐湿性の面で問題があるが、NiOとの固溶体とす
る事によつて、この点は改善される。従つて、こ
のMgxNi1-xO基板を用いて構成された磁気ヘツ
ドは優れた耐候・耐久特性を持つ。また基板材料
自体に関して、NiOとMgOの格子定数の差が小
さいために固溶体を形成しやすく、その上焼成時
の雰囲気も特に調節する必要がないために、製造
が容易である。
As a result of research, the inventors have developed a product with excellent moisture and heat resistance.
It has been found that by dissolving MgO in NiO, the coefficient of thermal expansion can be adjusted within the range of 100 to 140 x 10 -7 /°C. MgO is soluble in water,
Although there is a problem in terms of moisture resistance, this point can be improved by forming a solid solution with NiO. Therefore, a magnetic head constructed using this Mg x Ni 1-x O substrate has excellent weather resistance and durability characteristics. Regarding the substrate material itself, the difference in lattice constant between NiO and MgO is small, so it is easy to form a solid solution, and there is no need to particularly adjust the atmosphere during firing, so manufacturing is easy.

実施例 以下実施例を示す。Example Examples are shown below.

試薬特級の酸化ニツケルと酸化マグネシウムを
それぞれ秤量し、湿式ボールミルにて16時間混合
した後150℃で乾燥し、NiOとMgOのモル比が、
NiO:MgO=1:0,4:1,2:1,1:1,
1:2,1:4,0:1の混合粉末を得た。この
混合粉末に10重量%の純水を加え、造粒し、300
Kg/cm2の圧力で金型中で一軸加圧成形した。この
形成体をアルミナを圧力媒体としてSiCの型中に
入れ、1100℃〜1500℃の温度で、300Kg/cm2の圧
力で2時間、ホツトプレスした。得られた焼結体
は、X線回折により相の同定を、アルキメデス法
により密度測定を、走査型電子顕微鏡により粒径
観察を行ない、又、焼結体から5mm×5mm×10mm
の試料を切り出し熱膨張率計により25℃〜400℃
間における熱膨張係数の測定を行なつた。その結
果、X線回折では、いずれの試料においても岩塩
型結晶構造の回折パターンを示し、これにより焼
結体は、MgxNi1-xO(0<x<1)である事が確
認された。また密度測定結果は、NiOとMgOの
混合化によつて変化するが、いずれの試料におい
てもX線回折から求めた理論密度の99.5%以上で
あつた。走査電子顕微鏡観察から焼結体の粒径は
5〜10μmであつた。熱膨張係数は第1図に示し
たように、単一酸化物のMgO,NiOで140×10-7
程度と最大になり、Mg1/2Ni1/2Oで最小の100×
10-7/℃を示し、その間では連続的に変化した。
Reagent-grade nickel oxide and magnesium oxide were each weighed, mixed in a wet ball mill for 16 hours, and then dried at 150℃ to determine the molar ratio of NiO and MgO.
NiO:MgO=1:0, 4:1, 2:1, 1:1,
Mixed powders of 1:2, 1:4, and 0:1 were obtained. Add 10% by weight of pure water to this mixed powder, granulate it, and
Uniaxial pressure molding was carried out in a mold at a pressure of Kg/cm 2 . This formed body was placed in a SiC mold using alumina as a pressure medium, and hot pressed at a temperature of 1100°C to 1500°C and a pressure of 300 kg/cm 2 for 2 hours. The obtained sintered body was subjected to phase identification using X-ray diffraction, density measurement using Archimedes method, and particle size observation using a scanning electron microscope.
A sample was cut out and measured at 25℃ to 400℃ using a thermal dilatometer.
The coefficient of thermal expansion was measured between As a result, X-ray diffraction showed a rock salt-type crystal structure diffraction pattern for all samples, which confirmed that the sintered body was Mg x Ni 1-x O (0<x<1). Ta. The density measurement results varied depending on the mixture of NiO and MgO, but in all samples, the density was 99.5% or more of the theoretical density determined from X-ray diffraction. The grain size of the sintered body was found to be 5 to 10 μm as observed using a scanning electron microscope. As shown in Figure 1, the coefficient of thermal expansion is 140×10 -7 for single oxides MgO and NiO.
degree and maximum, and minimum 100× for Mg 1/2 Ni 1/2 O
10 -7 /°C, and it varied continuously between them.

そこで熱膨張係数が120×10-7/℃であるMg1/5
Ni4/5O(MgO:NiO=1:4)の焼結体をえら
び、切断・研磨して表面平滑度Rnax0.1μmの基板
とした。この基板と、熱膨張係数が120×10-7
℃のCoを主成分とする軟磁性アモルフアス合金
より、第2図に示すような磁気ヘツドを作成し
た。第2図中の1は基板、2は磁気ギヤツプ、3
はアモルフアス金属磁気膜、4は巻線用の窓であ
る。
Therefore, Mg 1/5 whose thermal expansion coefficient is 120×10 -7 /℃
A sintered body of Ni 4/5 O (MgO:NiO=1:4) was selected, cut and polished to obtain a substrate with a surface smoothness R nax of 0.1 μm. This substrate has a thermal expansion coefficient of 120×10 -7 /
A magnetic head as shown in Fig. 2 was fabricated from a soft magnetic amorphous alloy containing Co as a main component at a temperature of 1.5°C. In Figure 2, 1 is the board, 2 is the magnetic gap, and 3
4 is an amorphous metal magnetic film, and 4 is a window for winding.

磁気ヘツド作成の工程を説明すると、よく洗浄
した基板の上に、スパツタ装置で、SiO2を主成
分とする絶縁層を約1μmの厚さで形成し、次に軟
磁性アモルフアス合金薄膜を30μmの厚さで形成
する。この上に基板を無機接着剤でつけて、第2
図中のA,Bをつくる。Bには5の巻き線用窓と
なる溝を形成し、また、ギヤツプ形成用ガラス
を、A,B両部分の磁気ギヤツプ形成面に、スパ
ツタでつけ、最後にA,B部分を熱間接合する。
この接合体に巻き線をして、磁気ヘツドとなす。
To explain the process of creating a magnetic head, an insulating layer mainly composed of SiO 2 is formed to a thickness of about 1 μm on a well-cleaned substrate using a sputtering device, and then a soft magnetic amorphous alloy thin film is formed to a thickness of 30 μm. Form in thickness. A substrate is attached on top of this using an inorganic adhesive, and a second
Make A and B in the diagram. A groove is formed in B to serve as a window for the winding wire No. 5, and gap forming glass is sputtered to the magnetic gap forming surfaces of both parts A and B. Finally, parts A and B are hot bonded. do.
This bonded body is wound with wire to form a magnetic head.

このようにして作成したMg1/5Ni4/5O基板を用
いた磁気ヘツド以外に、比較のため、熱膨張係数
が120×10-7/℃の結晶化ガラスおよびCaO−
SrO−TiO2系セラミツクスを、それぞれ基板と
して用い、同様の方法で作成した磁気ヘツドを用
意した。これら三種の磁気ヘツドに対して、金属
磁性粉末を磁気記録媒体とした、いわゆる「メタ
ルテープ」を、相対速度約3.8m/secで摺動させ
て、ヘツドの出力変化・耐摩耗性・耐環境性をテ
ストした。その結果、通常の環境下、23℃、湿度
50%では、基板の種類による磁気ヘツド特性の差
は、特に見られなかつたが、環境条件が23℃、湿
度10%では、結晶化ガラスおよびCaO−SrO−
TiO2系セラミツクスを基板とした磁気ヘツドで
は、測定開始後数時間で、ヘツド出力が数dB低
下することが観察された。そこでこれらの磁気ヘ
ツドを詳しく観察すると、基板表面上に、磁気テ
ープの金属粉が付着し、凹凸が生じていた。一
方、本発明のMg1/5Ni4/5O基板には、このような
付着は起こらず、従つて磁気ヘツドの出力低下も
生じなかつた。また、他の環境条件下、高温多
湿、高温低湿、低温多湿でも同様のテストを行な
つたが、本発明のMg1/5Ni4/5O基板を用いた磁気
ヘツドでは、磁気ヘツド出力・耐摩耗性とも全く
問題を生ぜず、安定した特性を示した。一方、他
の基板材料を用いた磁気ヘツドでは、前述のよう
な出力低下や耐摩耗性等で問題を生じた。
In addition to the magnetic head using the Mg 1/5 Ni 4/5 O substrate prepared in this way, for comparison, crystallized glass with a thermal expansion coefficient of 120 × 10 -7 /°C and CaO-
Magnetic heads were prepared in the same manner using SrO-TiO 2 ceramics as substrates. A so-called "metal tape," which uses metal magnetic powder as a magnetic recording medium, was slid against these three types of magnetic heads at a relative speed of approximately 3.8 m/sec to improve the head's output changes, wear resistance, and environmental resistance. I tested the gender. As a result, under normal environment, 23℃, humidity
At 50%, there were no particular differences in magnetic head characteristics depending on the type of substrate, but under environmental conditions of 23°C and 10% humidity, crystallized glass and CaO-SrO-
In a magnetic head using a TiO 2 -based ceramic as a substrate, it was observed that the head output decreased by several dB within a few hours after the start of measurement. When these magnetic heads were closely observed, it was found that metal powder from the magnetic tape had adhered to the surface of the substrate, creating irregularities. On the other hand, such adhesion did not occur on the Mg 1/5 Ni 4/5 O substrate of the present invention, and therefore no reduction in the output of the magnetic head occurred. Similar tests were also conducted under other environmental conditions, such as high temperature and high humidity, high temperature and low humidity , and low temperature and high humidity. There were no problems with wear resistance, and stable characteristics were exhibited. On the other hand, magnetic heads using other substrate materials have had problems such as decreased output and wear resistance as described above.

耐摩耗性の面から考えると、摩耗量の大きすぎ
る基板材料は問題があり、また結晶構造に異方性
があると、結晶方位によつて摩耗量が異なり、基
板に凹凸が生じる事が考えられる。この点から考
えても、その結晶構造が岩塩型である基板材料は
要求特性を満たしたものである。
From the perspective of wear resistance, substrate materials that wear too much are problematic, and if the crystal structure has anisotropy, the amount of wear will vary depending on the crystal orientation, causing unevenness on the substrate. It will be done. From this point of view, a substrate material whose crystal structure is a rock salt type satisfies the required characteristics.

以上の実施例では、熱膨張係数が120×10-7
℃のアモルフアス磁性薄膜を用いる場合を示した
が、軟磁性材料としては、これに限らず、その熱
膨張係数が100×140×10-7/℃の範囲内のもので
あれば、それに応じて、NiOとMgOの固溶比率
を変える事により、最適の基板を提供する事がで
きるものである。また磁気ヘツドの作成法も、実
施例で述べた方法のみに限定するものではない。
In the above example, the coefficient of thermal expansion is 120×10 -7 /
℃ is used, but the soft magnetic material is not limited to this, and as long as its coefficient of thermal expansion is within the range of 100×140×10 -7 /℃, it can be By changing the solid solution ratio of NiO and MgO, an optimal substrate can be provided. Furthermore, the method of manufacturing the magnetic head is not limited to the method described in the embodiments.

第1図から明らかなように、熱膨張係数が100
〜104×10-7/℃を与える組成はNiOが多い側
(0<x<0.5)と、MgOが多い側(0.5<x<1)
があるが、どちらかを選ぶ場合にはNiOが多い側
を選んだ方が良い。NiOが多い方が焼結温度が低
くなり、また、MgOが多いと、耐湿性に問題を
生じてくる可能性があるためである。又、本発明
で用いる基板材料はMgxNi1-xOを主成分とし、
機械加工性を改善するためや、焼結特性を改善す
るため、添加物を添加しても、何ら問題を生じる
ものではない。
As is clear from Figure 1, the coefficient of thermal expansion is 100
The compositions that give ~104×10 -7 /℃ are the side with more NiO (0<x<0.5) and the side with more MgO (0.5<x<1)
However, if you have to choose between the two, it is better to choose the side with more NiO. This is because the more NiO there is, the lower the sintering temperature is, and the more MgO there is, the more moisture resistance may become a problem. Moreover, the substrate material used in the present invention has Mg x Ni 1-x O as a main component,
Addition of additives to improve machinability or sintering properties does not cause any problems.

発明の効果 本発明は、MgxNi1-xO(0<x<1)を主成分
とする熱膨張係数の調節された基板を用いた磁気
ヘツドであり、磁気記録媒体との摺動において問
題を生じる事なく安定した性能を有し、耐環境
性,耐摩耗性に優れたものである。
Effects of the Invention The present invention is a magnetic head using a substrate mainly composed of Mg x Ni 1-x O (0<x<1) and having an adjusted coefficient of thermal expansion. It has stable performance without any problems, and has excellent environmental resistance and wear resistance.

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

第1図はMgxNi1-xO系材料の熱膨張係数と組
成比xの値の関係を示す図、第2図は本発明によ
る磁気ヘツドの一例を示す図である。 1……基板、2……磁気ギヤツプ、3……アモ
ルフアス金属磁性膜、4……巻線用窓。
FIG. 1 is a diagram showing the relationship between the thermal expansion coefficient of Mg x Ni 1-x O-based material and the value of the composition ratio x, and FIG. 2 is a diagram showing an example of the magnetic head according to the present invention. 1... Substrate, 2... Magnetic gap, 3... Amorphous metal magnetic film, 4... Winding window.

Claims (1)

【特許請求の範囲】[Claims] 1 岩塩型結晶構造を持ち、複合酸化物Mgx
Ni1-xO(0<x<1)を主成分とする基板を用
い、この基板に磁気コアとして軟磁性材料を形成
した事を特徴とする磁気ヘツド。
1 Composite oxide Mg x with rock salt type crystal structure
A magnetic head characterized in that it uses a substrate mainly composed of Ni 1-x O (0<x<1) and has a soft magnetic material formed as a magnetic core on the substrate.
JP60032089A 1985-02-20 1985-02-20 Magnetic head Granted JPS61192005A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60032089A JPS61192005A (en) 1985-02-20 1985-02-20 Magnetic head

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60032089A JPS61192005A (en) 1985-02-20 1985-02-20 Magnetic head

Publications (2)

Publication Number Publication Date
JPS61192005A JPS61192005A (en) 1986-08-26
JPH0580044B2 true JPH0580044B2 (en) 1993-11-05

Family

ID=12349149

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60032089A Granted JPS61192005A (en) 1985-02-20 1985-02-20 Magnetic head

Country Status (1)

Country Link
JP (1) JPS61192005A (en)

Also Published As

Publication number Publication date
JPS61192005A (en) 1986-08-26

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