JPH0629151B2 - Sealing glass - Google Patents
Sealing glassInfo
- Publication number
- JPH0629151B2 JPH0629151B2 JP15711288A JP15711288A JPH0629151B2 JP H0629151 B2 JPH0629151 B2 JP H0629151B2 JP 15711288 A JP15711288 A JP 15711288A JP 15711288 A JP15711288 A JP 15711288A JP H0629151 B2 JPH0629151 B2 JP H0629151B2
- Authority
- JP
- Japan
- Prior art keywords
- glass
- ferrite
- head
- erosion
- coefficient
- 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 - Fee Related
Links
- 239000005394 sealing glass Substances 0.000 title description 4
- 239000011521 glass Substances 0.000 claims description 53
- 238000007789 sealing Methods 0.000 claims description 8
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 5
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical group 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 230000003628 erosive effect Effects 0.000 description 14
- 230000003014 reinforcing effect Effects 0.000 description 9
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 8
- 239000011162 core material Substances 0.000 description 5
- 238000010828 elution Methods 0.000 description 5
- HTUMBQDCCIXGCV-UHFFFAOYSA-N lead oxide Chemical compound [O-2].[Pb+2] HTUMBQDCCIXGCV-UHFFFAOYSA-N 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000011787 zinc oxide Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 229910052745 lead Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000005297 pyrex Substances 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- GCPXMJHSNVMWNM-UHFFFAOYSA-N arsenous acid Chemical compound O[As](O)O GCPXMJHSNVMWNM-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000004031 devitrification Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000006025 fining agent Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- YZXCQIOLVHGCFP-UHFFFAOYSA-N lead potassium Chemical compound [K].[Pb] YZXCQIOLVHGCFP-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL 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
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
- C03C8/24—Fusion seal compositions being frit compositions having non-frit additions, i.e. for use as seals between dissimilar materials, e.g. glass and metal; Glass solders
Landscapes
- 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)
- Glass Compositions (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明はフェライト磁気ヘッドの封着用ガラスに関する
ものである。TECHNICAL FIELD The present invention relates to a glass for sealing a ferrite magnetic head.
従来の技術 フェライトは磁気特性,耐摩耗性,機械加工性等が優れ
ているため、磁気ヘッド用コア材として広く用いられて
いる。第1図はフェライトをコア材としたビデオヘッド
の代表的な構造を示している。当ヘッドはフェライトコ
ア材1をギャップ巾に等しい間隔をおいて対向させ、そ
の空隙はギャップガラス2で形成され、補強ガラス3に
よって結合し、最後にコイル4を巻いて構成されてい
る。ギャップガラスは一般にSiO2やパイレックスガ
ラスの様な、高温でもフェライトと反応しにくい材料が
用いられ、その結果狭いギャップ巾を有するヘッドが安
定に得られている。2. Description of the Related Art Ferrite is widely used as a core material for magnetic heads because it has excellent magnetic properties, wear resistance, and machinability. FIG. 1 shows a typical structure of a video head using ferrite as a core material. This head is configured by facing ferrite core materials 1 with a gap equal to the gap width, the gap being formed by a gap glass 2, joined by a reinforcing glass 3, and finally winding a coil 4. As the gap glass, a material such as SiO 2 or Pyrex glass which hardly reacts with ferrite even at a high temperature is generally used, and as a result, a head having a narrow gap width is stably obtained.
一方、補強用ガラスは、コアを結合させるため、加熱時
に軟化、流動しなければならないが、この際あまり高温
にすると補強ガラスとフェライトの相互拡散が起こり、
トラック巾(TW)5が減少する。第2図はヘッドの上
面図を示し、本来(a)の様にTWが形成されるべきとこ
ろを、補強ガラスとフェライトの相互拡散によってTW
が減少した様子を(b)で示している。相互拡散した領域
の長さを侵食量6で示す。On the other hand, the reinforcing glass has to be softened and flown when heated in order to bond the core, but at this time, if the temperature is too high, mutual diffusion of the reinforcing glass and ferrite occurs,
Track width (TW) 5 is reduced. Fig. 2 shows a top view of the head, where the TW should originally be formed as shown in (a) by the mutual diffusion of the reinforcing glass and ferrite.
It is shown in (b) that the value has decreased. The length of the mutually diffused region is shown as an erosion amount 6.
上記加熱温度は通常750℃以下が用いられている。そ
れ以上高いとギャップガラスに用いられるパイレックス
ガラスが軟化したり、侵食を促進する。それゆえ補強ガ
ラスは750℃以下で流動し易いガラスが必要である。
また補強ガラスの熱膨張係数はフェライトのそれに近い
ことが必要である。一般にはその値は(90〜115)
×10-7/℃であるが、近年高解像度のテープに対応し
た飽和磁束密度の高いフェライトのそれは約130×1
0-7/℃にも達している(例えば堀川他、応用物理学会
予稿集4a−ZE−8(1985年10月))。The heating temperature is usually 750 ° C. or lower. If it is higher than that, the Pyrex glass used for the gap glass is softened or promotes erosion. Therefore, the reinforcing glass needs to be a glass that easily flows at 750 ° C or lower.
The coefficient of thermal expansion of the reinforced glass must be close to that of ferrite. Generally, the value is (90 ~ 115)
× 10 -7 / ° C, but in recent years, ferrite with a high saturation magnetic flux density, which is compatible with high resolution tapes, has a density of about 130 × 1.
It even reaches 0 −7 / ° C. (for example, Horikawa et al., Proceedings of the Japan Society of Applied Physics 4a-ZE-8 (October 1985)).
またヘッドは加工時に研磨工程を経る。この工程では水
が用いられるので、補強ガラスの耐水性が優れているこ
とが必要である。Further, the head undergoes a polishing process during processing. Since water is used in this step, it is necessary that the reinforced glass has excellent water resistance.
以上をまとめて、フェライトヘッド用補強ガラスに求め
られる条件を示すと、作業温度750℃以下で軟化、
流動しフェライトを侵食しないこと、熱膨張係数が
(90〜130)×10-7/℃であること、耐水性に
優れていることである。Summarizing the above, the conditions required for the reinforcing glass for a ferrite head are shown as follows: softening at a working temperature of 750 ° C. or lower,
They are to flow and not to erode the ferrite, to have a coefficient of thermal expansion of (90 to 130) × 10 −7 / ° C., and to be excellent in water resistance.
従来このような点を考慮した補強ガラスとして、(1)特
公昭49-8011号には作業温度700℃以下、熱膨張係数
(90〜110)×10-7/℃のガラス、(2)特開昭50-
32210,32211,32212,32213号には作業温度700〜75
0℃,熱膨張係数(90〜110)×10-7/℃のガラ
ス、(3)特開昭56-37246号には作業温度690〜770
℃、熱膨張係数(85〜110)×10-7/℃のガラ
ス、(4)特開昭57-55528号には作業温度350〜380
℃、熱膨張係数(110〜120)×10-7/℃のガラ
ス、(5)特開昭59-223248号公報には作業温度730℃、
熱膨張係数(92〜95)×10-7/℃のガラスが開示
されている。また(6)特開昭53-145825号公報にはフェラ
イト成分を含む、ZnOの含有量が3重量%以下である
ガラスが開示されている。Conventionally, as a reinforced glass that takes such points into consideration, (1) Japanese Patent Publication No. Sho 49-8011 discloses a glass having a working temperature of 700 ° C. or less and a coefficient of thermal expansion (90 to 110) × 10 −7 / ° C. Kaisho 50-
32210,32211,32212,32213 No. working temperature 700-75
Glass having a coefficient of thermal expansion (90 to 110) × 10 −7 / ° C. at 0 ° C. (3) Working temperature 690 to 770 in JP-A-56-37246
Glass having a coefficient of thermal expansion (85 to 110) × 10 −7 / ° C., (4) Working temperature of 350 to 380 in JP-A-57-55528.
Glass having a thermal expansion coefficient of (110 to 120) × 10 −7 / ° C., (5) Working temperature of 730 ° C. in JP-A-59-223248,
A glass having a coefficient of thermal expansion (92 to 95) × 10 −7 / ° C. is disclosed. (6) JP-A-53-145825 discloses a glass containing a ferrite component and having a ZnO content of 3% by weight or less.
発明が解決しようとする課題 しかしながら従来のガラスは必ずしも以下の点で満足で
きるものではなかった。すなわちフェライトを侵食する
ガラス成分として、発明者らはPb,Ba,Na等を見
出しているが、(1),(2)のガラスはPbO,Na2Oを
多く含み、(3),(5)のガラスはNa2O,BaOを多く
含み、(4)のガラスはPbOを多く含んでいるので、フ
ェライトを侵食し易いものであった。また(3),(5)はB
aO,B2O3,Na2Oを多く含んでいるので耐水性
が悪く、作業中に失透し易かった。また(4)もPbF2
を多く含んでいるので耐水性が悪かった。さらに以上の
ガラスには熱膨張係数が120×10-7/℃以上のもの
が無かった。他方(6)においては実施例としてフェライ
ト成分を約7.7%以上含有したガラスが開示されてい
るが、ガラスが濃く着色しているため、第3図で示した
ギャップの深さ7を規定の深さに調整する時にアペック
ス8が見えないといった問題点を有していた。DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention However, conventional glasses have not always been satisfactory in the following points. That is, the inventors have found Pb, Ba, Na and the like as glass components that erode ferrite, but the glasses (1) and (2) contain a large amount of PbO and Na 2 O, and (3), (5) Since the glass of () contains a large amount of Na 2 O and BaO, and the glass of (4) contains a large amount of PbO, it was easy to erode ferrite. Also, (3) and (5) are B
Since it contained a large amount of aO, B 2 O 3 and Na 2 O, it had poor water resistance and was easily devitrified during work. Also (4) is PbF 2
Since it contains a lot of water, the water resistance was poor. Furthermore, none of the above glasses had a coefficient of thermal expansion of 120 × 10 −7 / ° C. or more. On the other hand, in (6), a glass containing about 7.7% or more of a ferrite component is disclosed as an example, but since the glass is deeply colored, the gap depth 7 shown in FIG. 3 is specified. There was a problem that the Apex 8 could not be seen when adjusting to the depth of.
上記問題点に鑑み、本発明は新規組成の封着用ガラスを
提供することを目的とする。In view of the above problems, an object of the present invention is to provide a glass for sealing having a novel composition.
課題を解決するための手段 重量%でSiO2=30〜36%,B2O3=0〜5
%,PbO=29〜51%,ZnO+CdO=4〜20
%,Na2O=0〜5%,K2O=9〜16%,RO
(Rはアルカリ土類金属)=0〜5%,Al2O3=0
〜5%,As2O3またはSb2O3=0〜0.5%か
ら成る封着用ガラスである。望ましくは であるとより侵食抑制効果が大きい。さらにフェライト
の成分であるFe2O3,MnO2,NiOのうち少な
くとも1つを2%まで含有させるとさらに侵食は少なく
なる。Means for Solving the Problems SiO 2 = 30 to 36% by weight%, B 2 O 3 = 0 to 5
%, PbO = 29 to 51%, ZnO + CdO = 4 to 20
%, Na 2 O = 0 to 5%, K 2 O = 9 to 16%, RO
(R is an alkaline earth metal) = 0 to 5%, Al 2 O 3 = 0
5%, a sealing glass consisting of As 2 O 3 or Sb 2 O 3 = 0~0.5%. Preferably Is more effective in suppressing erosion. Further, if at least one of Fe 2 O 3 , MnO 2 , and NiO, which are ferrite components, is contained up to 2%, erosion is further reduced.
作用 本発明の封着用ガラスは耐水性に優れ、熱膨張係数とし
て(90〜130)×10-7/℃を有し、これを用いる
ことによりフェライトを侵食することが抑制され、トラ
ック巾の減少の少ないヘッドを容易に得ることができ
る。Action The sealing glass of the present invention has excellent water resistance and has a coefficient of thermal expansion of (90 to 130) × 10 −7 / ° C. By using this, corrosion of ferrite is suppressed and the track width is reduced. It is possible to easily obtain a head having a small number of heads.
実施例 フェライトを侵食させる成分Pb,Na,アルカリ土類
金属等の含有量を少なくし、これに代ってK,Zn,C
dを増すことにより、フェライトを侵食し難いガラスが
得られることを見出し種々の実験を行った。Example The contents of components Pb, Na, alkaline earth metals, etc. that attack ferrite are reduced, and instead of these, K, Zn, C are used.
It was found that by increasing d, glass that is less likely to erode ferrite was obtained, and various experiments were conducted.
表の試料NO.1〜72に本発明の封着用ガラスの30〜
300℃における熱膨張係数,軟化点,鉛溶出量および
侵食量(第2図b)を示す。試料NO.73〜90に本発
明の組成範囲外のガラスのそれらを示した。なお鉛溶出
量は200〜350メッシュのガラス粉末を100mlの
純水中にて1時間煮沸した際の上澄水中のPbイオンの
溶出量であり、耐水性の目安とした。すなわち鉛溶出量
が2ppm以下のガラスは、第1図のヘッドを60℃の純
水中に1時間浸漬しても、補強ガラス表面に曇りや荒れ
はほとんどなく、実用上差支えないものであった。なお
フェライト材としてはFe2O3=64モル%のMn−
Znフェライト(熱膨張係数=130×10-7/℃)、
ギャップガラスとしてSiO2を用い、ギャップ巾は
0.3μm、トラック巾は30μmのヘッドを試作し
た。Sample Nos. 1 to 72 in the table are 30 to 30 of the glass for sealing of the present invention.
The thermal expansion coefficient, softening point, lead elution amount and erosion amount at 300 ° C are shown (Fig. 2b). Samples Nos. 73-90 show those of glasses outside the composition range of the present invention. The lead elution amount is the elution amount of Pb ions in the supernatant water when 200 to 350 mesh glass powder was boiled in 100 ml of pure water for 1 hour, and was used as a measure of water resistance. That is, with respect to the glass having a lead elution amount of 2 ppm or less, even if the head shown in FIG. 1 was immersed in pure water at 60 ° C. for 1 hour, there was almost no clouding or roughening on the surface of the reinforcing glass, and there was no practical problem. . As the ferrite material, Fe 2 O 3 = 64 mol% of Mn-
Zn ferrite (coefficient of thermal expansion = 130 × 10 −7 / ° C.),
SiO 2 was used as the gap glass, and a head having a gap width of 0.3 μm and a track width of 30 μm was prototyped.
表より明らかなように、NO.1〜72のガラスは(92
〜130)×10-7/℃の熱膨張係数を有し、軟化点が
640℃以下であるため、750℃での流動性も良好で
あり、鉛溶出量は2.0ppm以下であるため耐水性が良
好であり、ヘッド化した場合の侵食量は2.0μm以下
と小さいものであった。As is clear from the table, the glass of NO.
To 130) × 10 -7 / ° C, the softening point is 640 ° C or less, so the fluidity at 750 ° C is also good, and the lead elution amount is 2.0 ppm or less, which is water resistant. The property was good, and the erosion amount when formed into a head was as small as 2.0 μm or less.
一方NO.73〜90のガラスでは侵食量が約2倍となっ
ており、フェライトを侵食し易く、正確なトラック巾が
得られなかった。On the other hand, in the glass of Nos. 73 to 90, the erosion amount was about twice, and the ferrite was easily eroded, and the accurate track width could not be obtained.
ここでSiO2は36%を超えるとガラスの軟化点が高
くなりすぎるため好ましくなく、30%より少ないと失
透し易くなる。Here, if SiO 2 exceeds 36%, the softening point of the glass becomes too high, which is not preferable, and if it is less than 30%, devitrification tends to occur.
B2O3は5%を超えるとガラスの耐水性を低くし、侵
食を大きくする。If B 2 O 3 exceeds 5%, the water resistance of the glass is lowered and the erosion is increased.
PbOは51%を超えると侵食を大きくし、29%より
少ないと作業温度が750℃以上になり好ましくない。When PbO exceeds 51%, erosion becomes large, and when it is less than 29%, the working temperature becomes 750 ° C. or higher, which is not preferable.
ZnOおよびCdOは20%を超えると軟化点が高くな
り、4%より少ないと侵食を抑える効果がない。またC
dOが多いほうが、より低軟化点のガラスとなり、作業
温度を下げられるので、侵食が小さくなる。When ZnO and CdO exceed 20%, the softening point becomes high, and when it is less than 4%, there is no effect of suppressing erosion. Also C
The more dO, the lower the softening point of the glass, and the lower the working temperature.
Na2Oは5%を超えると侵食を大きくする。Na 2 O increases erosion when it exceeds 5%.
K2Oは16%を超えるとガラスの耐水性を低くし、9
%より少ないと軟化点が高くなるとともに、侵食を抑え
る効果がない、RO,Al2O3は原料より不可避的に
混入する分も含めて5%以下にしないと、侵食を大きく
したり、軟化点を高くしすぎたりする。If K 2 O exceeds 16%, the water resistance of the glass decreases, and
If it is less than 5%, the softening point becomes high and there is no effect of suppressing erosion. If RO and Al 2 O 3 are not less than 5% including the amount that is inevitably mixed from the raw materials, the erosion will be increased or the softening will occur. The points are set too high.
As2O3またはSb2O3は清澄剤として0.5%以
下が適当である。As 2 O 3 or Sb 2 O 3 is suitable as a fining agent at 0.5% or less.
Fe2O3,MnO2,NiOのうち少なくとも1つは
フェライトの侵食をより小さくする働きがある。しかし
いずれも着色原料ともなるので、0.5〜2%が望まし
い。2%を超えると濃く着色して、第3図のアペックス
が見えなくなるからである。At least one of Fe 2 O 3 , MnO 2 , and NiO has a function of further reducing the corrosion of ferrite. However, all of them also serve as coloring materials, so 0.5 to 2% is preferable. This is because if it exceeds 2%, it will be deeply colored and the apex in FIG. 3 will not be visible.
以上のガラスは原料としてケイ砂,ホウ酸,鉛丹,酸化
亜鉛,酸化カドミウム,ソーダ灰,炭酸カリウム,亜ヒ
酸を用い、その他は相当する酸化物または炭酸塩を用い
ルツボとしてアルミナまたは白金ルツボを用い、130
0℃〜1400℃で30分〜1時間溶融し、水中急冷ま
たは双ローラー急冷にて採取した。その後作業し易いよ
うに直径1mmの線に加工してヘッドの試作に用いた。For the above glass, silica sand, boric acid, lead oxide, zinc oxide, cadmium oxide, soda ash, potassium carbonate, arsenous acid are used as raw materials, and other oxides or carbonates are used as the crucible for alumina or platinum crucible. Using 130
It was melted at 0 ° C. to 1400 ° C. for 30 minutes to 1 hour, and collected by water quenching or twin roller quenching. After that, it was processed into a wire with a diameter of 1 mm so that it could be easily worked, and used as a prototype of the head.
なお以上の説明においては磁気ヘッドへの適用について
述べたが、熱膨張係数の近接する金属(例えば白金,チ
タン,クロム鉄合金等)あるいはガラス(ソーダ石灰ガ
ラス,鉛カリガラス等)の接着や、CRTチューブの接
着,ハーメチックシール等にも適用可能であることは言
うまでもない。In the above description, application to a magnetic head has been described, but metal (for example, platinum, titanium, chromium-iron alloy, etc.) or glass (soda-lime glass, lead-potassium glass, etc.) having a similar coefficient of thermal expansion is bonded, or CRT is used. It goes without saying that it can also be applied to tube adhesion, hermetic sealing, etc.
発明の効果 以上のように本発明の封着用ガラスは、耐水性,流動
性,フェライトとの熱膨張係数の適合性に優れたもので
あり、特にフェライトを侵食することが少なく、トラッ
ク巾の減少の少ない磁気ヘッドが容易に得られるもので
ある。 EFFECTS OF THE INVENTION As described above, the glass for sealing of the present invention is excellent in water resistance, fluidity, and compatibility with the coefficient of thermal expansion of ferrite, and in particular, does not corrode ferrite and reduces track width. It is possible to easily obtain a magnetic head having a small amount.
第1図は本発明の一実施例の封着用ガラスを補強ガラス
として用いるビデオヘッドの構造図、第2図は同ヘッド
の上面図であり、(a)はトラック巾が正しく得られてい
る場合の状態図、(b)は侵食によってトラック巾が減少
している場合の状態図、第3図はヘッドのアベックス部
の拡大図である。 1……コア、2……ギャップガラス、3……補強ガラ
ス、4……コイル。FIG. 1 is a structural diagram of a video head using the sealing glass of one embodiment of the present invention as a reinforcing glass, and FIG. 2 is a top view of the same head. (A) shows a case where the track width is obtained correctly. (B) is a state diagram when the track width is reduced by erosion, and FIG. 3 is an enlarged view of the abex portion of the head. 1 ... Core, 2 ... Gap glass, 3 ... Reinforcing glass, 4 ... Coil.
Claims (3)
3=0〜5%,PbO=29〜51%,MO(MはZ
n,Cdの少なくとも1つをさす)=4〜20%,Na
2O=0〜5%,K2O=9〜16%,RO(Rはアル
カリ土類金属)=0〜5%,Al2O3=0〜5%,A
s2O3またはSb2O3=0〜0.5%から成ること
を特徴とする封着用ガラス。1. SiO 2 = 30-36% by weight, B 2 O
3 = 0 to 5%, PbO = 29 to 51%, MO (M is Z
n, at least one of Cd) = 4 to 20%, Na
2 O = 0 to 5%, K 2 O = 9 to 16%, RO (R is an alkaline earth metal) = 0 to 5%, Al 2 O 3 = 0 to 5%, A
Glass for sealing, comprising s 2 O 3 or Sb 2 O 3 = 0 to 0.5%.
着用ガラス。2. The glass for sealing according to claim 1, wherein:
くとも一種を0.5〜2重量%含有することを特徴とす
る特許請求の範囲第1項または第2項記載の封着用ガラ
ス。3. The glass for sealing according to claim 1 or 2, which contains 0.5 to 2% by weight of at least one of Fe 2 O 3 , MnO 2 and NiO.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15711288A JPH0629151B2 (en) | 1987-12-22 | 1988-06-24 | Sealing glass |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32461387 | 1987-12-22 | ||
| JP62-324613 | 1987-12-22 | ||
| JP15711288A JPH0629151B2 (en) | 1987-12-22 | 1988-06-24 | Sealing glass |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01252549A JPH01252549A (en) | 1989-10-09 |
| JPH0629151B2 true JPH0629151B2 (en) | 1994-04-20 |
Family
ID=26484672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15711288A Expired - Fee Related JPH0629151B2 (en) | 1987-12-22 | 1988-06-24 | Sealing glass |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0629151B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2734053B2 (en) * | 1989-01-31 | 1998-03-30 | ソニー株式会社 | Bonding glass and magnetic head |
| US8871664B2 (en) | 2010-05-10 | 2014-10-28 | Nippon Electric Glass Co., Ltd. | Refractory filler, sealing material using same, and manufacturing method for refractory filler |
| JP5773128B2 (en) * | 2010-05-10 | 2015-09-02 | 日本電気硝子株式会社 | Method for producing refractory filler |
| WO2011142215A1 (en) * | 2010-05-10 | 2011-11-17 | 日本電気硝子株式会社 | Fire-resistant filler, sealing material using same, and method for producing fire-resistant filler |
| JP5779922B2 (en) * | 2011-03-16 | 2015-09-16 | 日本電気硝子株式会社 | Refractory filler and sealing material using the same |
-
1988
- 1988-06-24 JP JP15711288A patent/JPH0629151B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01252549A (en) | 1989-10-09 |
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| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |