JPS6110082A - Sealing composition - Google Patents

Sealing composition

Info

Publication number
JPS6110082A
JPS6110082A JP13006484A JP13006484A JPS6110082A JP S6110082 A JPS6110082 A JP S6110082A JP 13006484 A JP13006484 A JP 13006484A JP 13006484 A JP13006484 A JP 13006484A JP S6110082 A JPS6110082 A JP S6110082A
Authority
JP
Japan
Prior art keywords
sealing
weight
arc tube
sealing material
ceramic
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.)
Granted
Application number
JP13006484A
Other languages
Japanese (ja)
Other versions
JPH0411511B2 (en
Inventor
繁 山崎
北川 満
勝美 高津
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.)
Iwasaki Denki KK
Original Assignee
Iwasaki Denki KK
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 Iwasaki Denki KK filed Critical Iwasaki Denki KK
Priority to JP13006484A priority Critical patent/JPS6110082A/en
Publication of JPS6110082A publication Critical patent/JPS6110082A/en
Publication of JPH0411511B2 publication Critical patent/JPH0411511B2/ja
Granted 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
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/24Fusion 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)
  • Ceramic Products (AREA)
  • Glass Compositions (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は透光性アルミナセラミックの封着材料に関し、
特にアルミナセラミック管を用いたメタル・・ライドラ
ンプの両端部に使用される封着用組成物の改良に関する
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a sealing material for translucent alumina ceramic.
In particular, it relates to improvements in sealing compositions used at both ends of metal ride lamps using alumina ceramic tubes.

従来の技術 近年、メタルハライドランプは高い効率と演色性の優れ
た実用的価値の高いランプとして照明の各分野で多用さ
れている。しかしながら、メタルハライドランプは、発
光管材料として石英を用いているために高圧ナトリウム
ランプの発光管材料として用いられているアルミナの様
な耐熱性の高いセラミック等に比較して使用温度限界が
低く、ランプのより高い効率と演色性を得ようとした時
、この使用温度限界が障害罠なっていた。メタルハライ
ドランプにおいては発光管の管壁負荷を高めるなどして
動作温度を高めると、より高い効率と演色性が得られる
が、この様な高い温度には石英が長時間耐えることがで
きないために、ランプの短寿命をもたらす結果となって
いた。
BACKGROUND OF THE INVENTION In recent years, metal halide lamps have been widely used in various fields of lighting as lamps with high efficiency and excellent color rendering properties and high practical value. However, since metal halide lamps use quartz as the arc tube material, the operating temperature limit is lower than that of highly heat-resistant ceramics such as alumina, which are used as the arc tube material of high-pressure sodium lamps. When trying to obtain higher efficiency and color rendering properties, this operating temperature limit has become a stumbling block. In metal halide lamps, higher efficiency and color rendering can be obtained by increasing the operating temperature by increasing the wall load of the arc tube, but since quartz cannot withstand such high temperatures for long periods of time, This resulted in a shortened lamp life.

メタルハライドランプ動作中の発光管の最高温度は発光
管管体の中心部にあり、動作可能温度はこの部分の温度
によって規制され発光管端部の保温板等の大きさによっ
て任意の蒸気圧が得られる様に構成されている。そこで
メタルハライドランプの動作温度を上げ、より高い効率
と演色性を得るために、石英製発光管に代えて、石英よ
りも耐熱性と化学的安定性の高いアルミナセラミック管
等を用いることが種々試みられている。
The maximum temperature of the arc tube during operation of the metal halide lamp is at the center of the arc tube body, and the operating temperature is regulated by the temperature of this area, and any vapor pressure can be obtained depending on the size of the heat insulating plate at the end of the arc tube. It is configured so that it can be used. Therefore, in order to raise the operating temperature of metal halide lamps and obtain higher efficiency and color rendering, various attempts have been made to use alumina ceramic tubes, etc., which have higher heat resistance and chemical stability than quartz, instead of quartz arc tubes. It is being

このセラミック製発光管を用いたメタルハライトランプ
において、発光管端部の封着材料として、例えばイギリ
ス特許8,010,906号記載の5102− At2
0.− MgO系封着材、特公昭49−32301号記
載のBeO−AA2C)5−5i02 系封着材等が知
られている。これらの封着材を使用する際、まず発光管
の一端がシールされ、充填ガス及び添加物を封入した後
、他端をシールするが、この他端のシール時においてシ
ールするだめの条件すなわち温度と時間は添加物の揮発
による損失あるいは充填ガスの純度低下を最小限に抑え
るように選定される。すなわち、シール時の温度は比較
的低温で、かつ短時間でシールが完成されなければなら
ないが、前記の如き封着用組成中前者はシール時の急激
な熱衝撃とアルミナセラミックとのわずかな膨張率の違
いにより、溶融固化後の封着柱内部に微細なりラックが
多数発生し、発光管点灯と同時にこのクラックが拡大さ
れリークに至る例が多かった。又、後者の組成では封着
時の溶融封着材の粘性が高く、固化後セラミックキャッ
プとノくイブとの間の間隙が大となム リークしやすく
なったり、粘性が高いために気泡を取り込んだりして、
シール不良が発生しやすかった。又、アルミナとの接着
強度に実用上の問題があった。更に、このような封着材
は点灯中の高温のハロゲン蒸気に対する耐ハロゲン性お
よび封着作業の際の溶融温度を考慮する必要がある。
In this metal halide lamp using a ceramic arc tube, as a sealing material for the end of the arc tube, for example, 5102-At2 described in British Patent No. 8,010,906 is used.
0. - MgO-based sealing materials, BeO-AA2C)5-5i02-based sealing materials described in Japanese Patent Publication No. 49-32301, and the like are known. When using these sealing materials, one end of the arc tube is first sealed, the filler gas and additives are sealed, and then the other end is sealed. and time are selected to minimize losses due to volatilization of additives or loss of purity of the fill gas. In other words, the temperature during sealing must be relatively low and the seal must be completed in a short time, but among the sealing compositions mentioned above, the former has a rapid thermal shock during sealing and a small expansion coefficient with alumina ceramic. Due to this difference, many fine cracks were generated inside the sealing column after melting and solidification, and in many cases, these cracks expanded when the arc tube was turned on, leading to leakage. In addition, with the latter composition, the viscosity of the molten sealing material during sealing is high, and after solidification, the gap between the ceramic cap and the nozzle tube becomes large, making it easy for leaks to occur. I took it in,
Seal failure was likely to occur. In addition, there was a practical problem in the adhesive strength with alumina. Furthermore, it is necessary to consider the halogen resistance of such a sealing material to high-temperature halogen vapor during lighting and the melting temperature during sealing work.

発明が解決しようとする問題点 本発明は上記の点に鑑みなされたもので、セラミックと
セラミック又はセラミックと金属とを封着するための封
着用組成物としてAt20う、Y2Oう、L&205.
5102およびBeOを所定の組成比(重量%)に選定
することにより、耐ノ・ロゲン性が高く、溶融固化後の
微細クラック及び気泡の発生がなく、かつ接着強度の高
い封着材を得ることができ長寿命、高効率、高演色性を
有するセラミック製メタルハライドランプを提供するこ
とを目的とする。
Problems to be Solved by the Invention The present invention has been made in view of the above points, and uses At20, Y2O, L&205.
By selecting a predetermined composition ratio (wt%) of 5102 and BeO, a sealing material with high corrosion resistance, no generation of microcracks or bubbles after melting and solidification, and high adhesive strength can be obtained. The purpose of the present invention is to provide a ceramic metal halide lamp that has a long life, high efficiency, and high color rendering properties.

問題点を解決するための手段 本発明者等はかかる封着材について多くの実験を重ねた
結果、ht2o、 (酸化アルミニウム)、Y2O5(
酸化イツトリウム) 、La2C15(酸化う/り/)
、5io2  (二酸化珪素)及びBeo (酸化べ1
71Jウム)のように耐ハロゲン性の高い成分を選定し
た。ここで、酸化ベリリウムは適量の添加によりアルミ
ナ基体との間に界面反応が生じ接着強度が大きく溶融時
粘性の低下が可能であることを見出し、良好な封着材が
得られることを確認した。
Means for Solving the Problems As a result of many experiments with such sealing materials, the inventors found that ht2o, (aluminum oxide), Y2O5 (
Yttrium oxide), La2C15 (U/Li/)
, 5io2 (silicon dioxide) and Beo (silicon dioxide)
A component with high halogen resistance, such as 71 Jum), was selected. Here, it was discovered that by adding an appropriate amount of beryllium oxide, an interfacial reaction occurs between the beryllium oxide and the alumina substrate, resulting in high adhesive strength and a reduction in viscosity when melted, and it was confirmed that a good sealing material can be obtained.

本発明は上記実験結果に基づいて完成されたものであり
、その成分は次の含有組成をもつものである。
The present invention was completed based on the above experimental results, and its components have the following composition.

At205:  5〜30重量% Y2O5:10〜40重量% La2()5 : 30−70重it%5102:5〜
30重量% 8eO:2−15重量% 作用 上記の組成限定理由は、次の様なことに依る。
At205: 5-30% by weight Y2O5: 10-40% by weight La2()5: 30-70% by weight 5102: 5-
30% by weight 8eO: 2-15% by weight Function The reason for the above compositional limitation is as follows.

At205量を30重量%以上とすると、封着材中に気
泡が多くなり結晶の析出が大となり、クラックが多発し
、5IO2量を30重量−以上とすると、融点降下が徹
しくなり、実用上問題となり、かつ熱膨張率がht2o
3のそれよりも小さくなりすぎクラックが生じる。Y2
O3景を40重11%以上とすると、融点が1500℃
以上となり、実用上問題となり、BeO量を15重量%
以上とすると、結晶性が大となりすぎ、気泡、クランク
が生じる。
If the amount of At205 is 30% by weight or more, there will be many bubbles in the sealing material, crystal precipitation will be large, and cracks will occur frequently, and if the amount of 5IO2 is 30% by weight or more, the melting point will be severely lowered, making it practically problem, and the coefficient of thermal expansion is ht2o
If it becomes too small than that of No. 3, cracks will occur. Y2
If the O3 concentration is 40% by weight or more, the melting point is 1500℃.
This caused a practical problem, and the amount of BeO was reduced to 15% by weight.
If it is more than that, the crystallinity becomes too large and bubbles and cranks are generated.

L & 203量を70重量−以上とすると、気泡、ク
ラックが多発し、リークしやすくなる。次に下限の限定
理由を述べると、5102、Be01At205、Y2
O。
If the amount of L & 203 is 70% by weight or more, bubbles and cracks will occur frequently and leakage will occur easily. Next, to explain the reason for the lower limit, 5102, Be01At205, Y2
O.

量を限定値以下とすると融点上昇が大となり実用上問題
となりLJO5を30重量%以下とすると、結晶の析出
が大きくなりすぎ結晶間にクラックが多発しリークしや
すくなる。
If the amount is less than the limited value, the melting point will increase significantly, which is a practical problem. If LJO5 is less than 30% by weight, the precipitation of crystals will become too large, resulting in frequent cracks between crystals, making it easy to leak.

従って、上記成分比内に各成分を調整することによって
、耐ハロゲン性が高く、アルミナセラミックとの熱膨張
係数も許容限度内に合致し、更に融点も1200〜14
50℃以内の実用上全く問題のない封着材が得られるこ
とがわかった。
Therefore, by adjusting each component within the above component ratio, halogen resistance is high, the coefficient of thermal expansion with alumina ceramic is within the permissible limit, and the melting point is 1200 to 14.
It was found that a sealing material having a temperature of 50° C. or less without any practical problems could be obtained.

実施例 次に、本発明にかかる実施例を封着材の調合法とともに
述べる。
Examples Next, examples according to the present invention will be described together with a method of preparing a sealing material.

第1表に示す様な調合用原料を粉砕混合した後、所望の
形状に圧縮成形したものをセラミック管の端部とエンド
キャップとの封着部に配置し、同封着部を真空あるいは
希ガス中で1,400〜1.600℃に加熱することに
よって回部を封着する。第1表中の実施例N11l〜N
[L4において特性的に異なるのは単に封着時における
融点が多少異なることと、結晶相とガラス相との比率が
多少異なるのみであり、気泡はほとんどなく、クラック
もなく気密性は良好であった。
After pulverizing and mixing the raw materials for preparation as shown in Table 1, the mixture is compression-molded into the desired shape and placed in the sealing area between the end of the ceramic tube and the end cap, and the sealing area is vacuumed or inert gas The round part is sealed by heating to 1,400 to 1,600°C in the inside. Examples N11l to N in Table 1
[The only difference in characteristics in L4 is that the melting point at the time of sealing is slightly different, and the ratio between the crystal phase and the glass phase is slightly different; there are almost no bubbles, no cracks, and the airtightness is good. Ta.

この様に前記実施例とさらに種々実験結果を組合せると
封着材組成として At205:5〜30重量% Y2O5:10〜40重量% La2O3: 30〜70重量% 5IO2:5〜30重量% BeO:  2−15重量% の範囲からなる封着材であれば、十分満足すべき封止状
態が得られることが明らかとなった。
In this way, by combining the above examples and various experimental results, the composition of the sealing material is At205: 5-30% by weight Y2O5: 10-40% by weight La2O3: 30-70% by weight 5IO2: 5-30% by weight BeO: It has become clear that a sufficiently satisfactory sealing state can be obtained with a sealing material in the range of 2-15% by weight.

この様に、管内に沃化タリウム、沃化ディスプロシウム
を各所定量封入した透光性アルミナセラミック発光管を
用いたメタルハライドランプを作成して、点灯試験を長
時間行ったが、封止部のリークは全く見られなかった。
In this way, we created a metal halide lamp using a translucent alumina ceramic arc tube with predetermined amounts of thallium iodide and dysprosium iodide sealed inside the tube, and conducted lighting tests for a long time. No leaks were observed.

発明の効果 以上の説明から明らかなように1本発明に係る封着用組
成物はセラミックとセラミック又はセラミックと金属と
を封着した際、封着付内部に微細なりラックおよび気泡
が生じることがなく、接着強度も高く更に耐ハロゲン性
に優れているのでリ一りによるランプの不点事故を防止
することができる。
Effects of the Invention As is clear from the above explanation, when the sealing composition according to the present invention seals ceramics to ceramics or ceramics to metals, fine racks and air bubbles are not generated inside the bonded area. Since it has high adhesive strength and excellent halogen resistance, it can prevent lamp malfunctions due to cracking.

又、封着材の融点を適切な範囲に選定できるので、作業
性が良い等の利点を有する。
Further, since the melting point of the sealing material can be selected within an appropriate range, there are advantages such as good workability.

Claims (1)

【特許請求の範囲】[Claims] 5〜30重量%のAl_2O_3、10〜40重量%の
Y_2O_3、30〜70重量%のLa_2O_3、5
〜30重量%のSiO_2及び2〜15重量%のBeO
を含有してなるセラミックとセラミック又はセラミック
と金属とを封着するための封着用組成物。
5-30% by weight Al_2O_3, 10-40% by weight Y_2O_3, 30-70% by weight La_2O_3, 5
~30 wt% SiO_2 and 2-15 wt% BeO
A sealing composition for sealing a ceramic and a ceramic or a ceramic and a metal.
JP13006484A 1984-06-26 1984-06-26 Sealing composition Granted JPS6110082A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13006484A JPS6110082A (en) 1984-06-26 1984-06-26 Sealing composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13006484A JPS6110082A (en) 1984-06-26 1984-06-26 Sealing composition

Publications (2)

Publication Number Publication Date
JPS6110082A true JPS6110082A (en) 1986-01-17
JPH0411511B2 JPH0411511B2 (en) 1992-02-28

Family

ID=15025150

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13006484A Granted JPS6110082A (en) 1984-06-26 1984-06-26 Sealing composition

Country Status (1)

Country Link
JP (1) JPS6110082A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006106781A1 (en) * 2005-03-31 2006-10-12 Nippon Sheet Glass Company, Limited Glass composition containing yttrium and glass spacer for electron beam excitation type display
JP2011195440A (en) * 2010-03-19 2011-10-06 Schott Ag Glass-ceramic as dielectric for use in high-frequency range

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006106781A1 (en) * 2005-03-31 2006-10-12 Nippon Sheet Glass Company, Limited Glass composition containing yttrium and glass spacer for electron beam excitation type display
JP2011195440A (en) * 2010-03-19 2011-10-06 Schott Ag Glass-ceramic as dielectric for use in high-frequency range

Also Published As

Publication number Publication date
JPH0411511B2 (en) 1992-02-28

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