JPS6142776B2 - - Google Patents
Info
- Publication number
- JPS6142776B2 JPS6142776B2 JP17574682A JP17574682A JPS6142776B2 JP S6142776 B2 JPS6142776 B2 JP S6142776B2 JP 17574682 A JP17574682 A JP 17574682A JP 17574682 A JP17574682 A JP 17574682A JP S6142776 B2 JPS6142776 B2 JP S6142776B2
- Authority
- JP
- Japan
- Prior art keywords
- alloy
- thermal expansion
- coefficient
- sealing
- less
- 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
Links
- 229910045601 alloy Inorganic materials 0.000 claims description 20
- 239000000956 alloy Substances 0.000 claims description 20
- 239000011521 glass Substances 0.000 claims description 15
- 238000007789 sealing Methods 0.000 claims description 15
- 229910000640 Fe alloy Inorganic materials 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000007542 hardness measurement Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
Landscapes
- Joining Of Glass To Other Materials (AREA)
Description
この発明は強度の大なる軟質ガラス封着用合金
に関する。
一般に軟質ガラス封着用合金としては42Ni―
6Cr―Fe合金や4.7Ni―5Cr―Fe合金等が広く使
用される。通常、これらの合金は所要形状に打抜
加工あるいはエツチング加工した後、湿潤水素中
で酸化被膜処理を施してガラス封着され、ブラウ
ン管のアノードボタンやデジタル表示管のリード
フレーム等に使用されている。
ところで最近、デジタル表示管が自動車等に採
用されるようになつたが、デジタル表示管の上記
封着用合金は打抜加工部あるいはエツチング加工
部の強度が不足し、そのため自動車の走行中の振
動で折損し易いと伝う問題が生じ、また省資源の
ため合金板を薄肉化したと伝う要望から、高硬度
を有する封着用合金への需要が大となつてきた。
本発明はかゝる需要に応じ得る合金の開発を目
的とするものであり、発明者は40〜48wt%Ni、
4〜8wt%Cr、Fe封着用合金の熱膨脹係数を変
化させずに所要の酸化被膜処理の硬度を上昇せし
める合金元素について種々実験研究した結果、上
記合金にBeおよびCを特定量含有させることに
より、従来の封着用合金の熱膨脹係数および酸化
被膜の接着強度を劣下させず硬度を上昇せしめ得
ることを発見した。
本発明は上記知見に基くものであつて、
Ni4048wt%、Cr4〜8wt%、Si0.10〜0.40wt%、
Mn0.10〜0.40wt%、Al0.05〜0.40wt%と
C0.015wt%以下、Be0.05〜0.50wt%を含有し、
残部は実質的にFeからなる強度大なる軟質ガラ
ス封着用合金を要旨とする。
本発明において、成分範囲を上記の如く限定し
た理由を次に説明する。
Ni40%未満では熱膨脹係数が小さくなりすぎ
て、軟質ガラスとの熱膨脹係数差が大となり、ガ
ラス封着が困難となる。また48%を越えると熱膨
脹係数が大きくなりすぎて軟質ガラスとの熱膨脹
係数差が大となりすぎるので好ましくない。
またCrは40%未満では熱膨脹係数が小さくな
りすぎ、軟質ガラスとの熱膨脹係数差が大きくな
りすぎるとともに、酸化被膜の合金素地との密着
性が悪くなり、8%を越えると熱膨脹係数が大き
くなりすぎて軟質ガラスとの熱膨脹係数差が大き
くなりすぎ好ましくない。
Siは0.10%未満では生成酸化被膜の合成素地と
の密着性が悪く、0.40%を越えると熱間加工性を
劣化させるので好ましくない。
Mnは原料より混入するSをMnSに固定して熱
間加工性の改善に有効であるが、0.10%より少な
いとその効果が少なく、また0.40%を越える領域
ではその効果が飽和するので、それ以上の含有は
必要ない。
Alは酸化被膜の合成素地への密着性改善に効
果があるが、0.05%未満ではその効果がなく、ま
た0.40%を越えての添加は熱間加工性を劣化させ
るので好ましくない。
本発明の特徴であるBeは硬度上昇に有効であ
る。しかし0.05%未満ではその効果が少なく、ま
た0.50%を越えると熱間加工性を劣化させる。
Cは0.015%より上ではガラス封着時、Cがガ
ラス中のO2と反応してCOガスを発生し、封着用
低融点ガラス中に気泡を生成し、ガラス封着強度
を低下させるので好ましくない。C0.015%以下
では特に発泡はなく、封着強度向上に有効であ
る。また本発明合金では、O2+N2を0.010%以下
にすることにより、封着時ガラス気泡の生成防止
および加工性改善に有効である。
以下本発明を実施例により説明する。
第1表に成分を掲げた本発明合金および比較合
金を熱間圧延後、軟化焼鈍し、その後最終加工率
80%にて冷間圧延した板厚0.2mm×巾340mm×長さ
5.000mmの板より硬度測定用試料を採取し、ヴイ
カース硬度を測定した。
また熱膨脹特性は前記熱間圧延材より3mm×
50mmの試料を採取し、900℃×30分の熱処理後測
定した。
同表は圧延のまま、および各温度で20分保持し
た熱処理の場合の各試料の硬度および各温度範囲
での平均熱膨脹係数を表わす。
This invention relates to a soft glass sealing alloy with high strength. 42Ni is generally used as an alloy for soft glass sealing.
6Cr-Fe alloy and 4.7Ni-5Cr-Fe alloy are widely used. Normally, these alloys are punched or etched into the desired shape, then treated with an oxide film in wet hydrogen and sealed with glass, and are used for things such as cathode ray tube anode buttons and digital display tube lead frames. . By the way, recently, digital display tubes have been used in automobiles, etc., but the above-mentioned sealing alloy of digital display tubes lacks strength in the punched or etched portions, and as a result, it is susceptible to vibrations while the automobile is running. Due to the problem of easy breakage and the desire to make alloy plates thinner in order to save resources, demand for sealing alloys with high hardness has increased. The purpose of the present invention is to develop an alloy that can meet such demands, and the inventor has developed an alloy that can meet such demands.
As a result of various experimental studies on alloying elements that increase the hardness of the necessary oxide coating treatment without changing the thermal expansion coefficient of the sealing alloy with 4 to 8 wt% Cr and Fe, we found that by adding specific amounts of Be and C to the above alloy. discovered that the hardness of conventional sealing alloys can be increased without deteriorating the coefficient of thermal expansion or the adhesive strength of the oxide film. The present invention is based on the above findings, and includes:
Ni4048wt%, Cr4~8wt%, Si0.10~0.40wt%,
Mn0.10~0.40wt%, Al0.05~0.40wt%
Contains C0.015wt% or less, Be0.05~0.50wt%,
The remainder consists of a strong soft glass sealing alloy consisting essentially of Fe. In the present invention, the reason why the component range is limited as described above will be explained below. If Ni is less than 40%, the coefficient of thermal expansion becomes too small, and the difference in coefficient of thermal expansion with soft glass becomes large, making glass sealing difficult. Moreover, if it exceeds 48%, the coefficient of thermal expansion becomes too large and the difference in coefficient of thermal expansion with soft glass becomes too large, which is not preferable. Furthermore, if Cr is less than 40%, the coefficient of thermal expansion will be too small, and the difference in coefficient of thermal expansion with soft glass will become too large, and the adhesion of the oxide film to the alloy base will be poor, and if it exceeds 8%, the coefficient of thermal expansion will become too large. If it is too large, the difference in coefficient of thermal expansion with soft glass will become too large, which is not preferable. If Si is less than 0.10%, the adhesion of the formed oxide film to the synthetic substrate is poor, and if it exceeds 0.40%, hot workability is deteriorated, which is not preferable. Mn is effective in improving hot workability by fixing S mixed in the raw material into MnS, but if it is less than 0.10%, the effect is small, and if it exceeds 0.40%, the effect is saturated. It is not necessary to contain more than that. Al is effective in improving the adhesion of the oxide film to the synthetic substrate, but if it is less than 0.05%, it has no effect, and if it is added in excess of 0.40%, it deteriorates hot workability, which is not preferable. Be, which is a feature of the present invention, is effective in increasing hardness. However, if it is less than 0.05%, the effect will be small, and if it exceeds 0.50%, hot workability will deteriorate. If C exceeds 0.015%, C reacts with O 2 in the glass to generate CO gas during glass sealing, creating bubbles in the low melting point glass for sealing and reducing the glass sealing strength, so it is preferable. do not have. When C is 0.015% or less, there is no particular foaming and it is effective in improving the sealing strength. Furthermore, in the alloy of the present invention, by controlling O 2 +N 2 to 0.010% or less, it is effective in preventing the formation of glass bubbles during sealing and improving processability. The present invention will be explained below with reference to Examples. After hot rolling, the present invention alloy and comparative alloy whose components are listed in Table 1 are softened and annealed, and then the final processing rate is
80% cold rolled plate thickness 0.2mm x width 340mm x length
A sample for hardness measurement was taken from a 5.000 mm plate, and the Vikers hardness was measured. In addition, the thermal expansion characteristics are 3 mm
A 50 mm sample was taken and measured after heat treatment at 900°C for 30 minutes. The table shows the hardness and average coefficient of thermal expansion of each sample in each temperature range when rolled and after heat treatment at each temperature for 20 minutes.
【表】【table】
【表】
第1表より明かな如く、本発明合金は従来の封
着用合金の42Ni―6Cr―Fe合金や47Ni―5Cr―Fe
合金の熱膨脹係数の差は殆んどなく、しかも硬度
が一段と向上している。
従つて本発明は、例えば自動車用デジタル表示
管のリードフレーム材の寿命を延長し、また板厚
を薄肉化できるので省資源や費用の節約を図るこ
とができる。[Table] As is clear from Table 1, the alloy of the present invention is the conventional sealing alloy 42Ni-6Cr-Fe alloy and 47Ni-5Cr-Fe alloy.
There is almost no difference in the coefficient of thermal expansion of the alloys, and the hardness is further improved. Therefore, the present invention can extend the life of the lead frame material of, for example, a digital display tube for automobiles, and can also reduce the thickness of the lead frame, thereby saving resources and costs.
Claims (1)
%、Mn0.10〜0.40wt%、Al0.05〜0.40wt%と
C0.015wt%以下、Be0.05〜0.50wt%を含有し、
残部は実質的にFeからなることを特徴とする強
度大なる軟質ガラス封着用合金。1 Ni40~48wt%, Cr4~8wt%, Si0.10~0.4wt
%, Mn0.10~0.40wt%, Al0.05~0.40wt%
Contains C0.015wt% or less, Be0.05~0.50wt%,
An alloy for soft glass sealing with great strength, characterized in that the remainder essentially consists of Fe.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17574682A JPS5964749A (en) | 1982-10-05 | 1982-10-05 | Soft glass sealing alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17574682A JPS5964749A (en) | 1982-10-05 | 1982-10-05 | Soft glass sealing alloy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5964749A JPS5964749A (en) | 1984-04-12 |
| JPS6142776B2 true JPS6142776B2 (en) | 1986-09-24 |
Family
ID=16001521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17574682A Granted JPS5964749A (en) | 1982-10-05 | 1982-10-05 | Soft glass sealing alloy |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5964749A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6164853A (en) * | 1984-09-06 | 1986-04-03 | Toshiba Corp | Base material for pipe parts and its manufacture |
| US5264052A (en) * | 1988-12-14 | 1993-11-23 | Yamaha Corporation | Fe-Ni alloy and method for producing the same |
-
1982
- 1982-10-05 JP JP17574682A patent/JPS5964749A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5964749A (en) | 1984-04-12 |
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