JPH01102829A - Cathode of electron tube and its manufacture - Google Patents

Cathode of electron tube and its manufacture

Info

Publication number
JPH01102829A
JPH01102829A JP62259695A JP25969587A JPH01102829A JP H01102829 A JPH01102829 A JP H01102829A JP 62259695 A JP62259695 A JP 62259695A JP 25969587 A JP25969587 A JP 25969587A JP H01102829 A JPH01102829 A JP H01102829A
Authority
JP
Japan
Prior art keywords
earth metal
alkaline earth
powder
ba3sc4o9
oxide layer
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
JP62259695A
Other languages
Japanese (ja)
Inventor
Takao Kawamura
河村 孝男
Hiroshi Kawasaki
浩 川崎
Katsuo Yuhara
克夫 湯原
Shunji Saito
斉藤 駿次
Seiji Kumada
熊田 政治
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.)
Hitachi Ltd
Japan Display Inc
Original Assignee
Hitachi Device Engineering Co Ltd
Hitachi 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 Hitachi Device Engineering Co Ltd, Hitachi Ltd filed Critical Hitachi Device Engineering Co Ltd
Priority to JP62259695A priority Critical patent/JPH01102829A/en
Publication of JPH01102829A publication Critical patent/JPH01102829A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To shorten the aging time, provide good initial characteristic, and prolong the life with high current density by allowing an alkaline earth metal oxide layer to contain dispersed powder of Ba3Sc4O9. CONSTITUTION:0.1-20wt.% Ba3Sc4O9 powder prepared previously is dispersed uniformly in an alkaline earth metal oxide layer. That is, barium carbonate (changed into barium oxide already at the time of reaction) and scandium oxide are mixed and heated for a sufficiently long time, and Ba3Sc4O9 as product is added dispersedly in the alkali earth metal oxide layer. Thereby Ba3Sc4O9 is distributed uniformly in electron emitting substance to allow acquistion of highly uniform and stable electron emitting characteristics from the initial period.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は高い電流密度で長期間安定した電子放出特性を
示す電子管陰極及びその製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an electron tube cathode that exhibits stable electron emission characteristics over a long period of time at high current density, and a method for manufacturing the same.

〔従来の技術〕[Conventional technology]

カラー受像管、表示管や撮像管の高精細度化に伴って、
これらの電子管の陰極には、高電流密度で長期間安定し
た電子放出特性を有することが強く要望されるようにな
った。
With the increasing definition of color picture tubes, display tubes, and image pickup tubes,
There is a strong demand for the cathodes of these electron tubes to have electron emission characteristics that are stable at high current densities over long periods of time.

これらの要望に応えるために、例えば特開昭61−27
1732号公報には、アルカリ土類金属酸化物層に酸化
スカンジウムの粉末を分散させたものが開示されている
。このアルカリ土類金属酸化物中に分散している酸化ス
カンジウム粉末は、アルカリ土類金属酸化物、例えばB
aOと反応して生成された複合酸化物Ba工5cyO□
が電子放出物質中に分散し、この複合酸化物が陰極の動
作中に熱分解を起こして遊ii!lBaを生成し易くす
る。そのため、板金アルカリ土類金属酸化物と基体金属
中にii&量に含まれているSt、 Mg等の還元性元
素による反応によって中間層が形成され、この中間層に
より遊離Baの生成が抑制されたとしても、遊MBaの
晋が不足することはなくなる。
In order to meet these demands, for example, Japanese Patent Laid-Open No. 61-27
Japanese Patent No. 1732 discloses an alkaline earth metal oxide layer in which scandium oxide powder is dispersed. The scandium oxide powder dispersed in this alkaline earth metal oxide is an alkaline earth metal oxide, such as B
Composite oxide Ba-5cyO produced by reaction with aO
is dispersed in the electron-emitting material, and this composite oxide undergoes thermal decomposition during operation of the cathode and is released ii! Make it easier to generate lBa. Therefore, an intermediate layer was formed by the reaction between the sheet metal alkaline earth metal oxide and reducing elements such as St and Mg contained in the base metal, and this intermediate layer suppressed the generation of free Ba. Even so, there will be no shortage of talent among playing MBas.

また、複を含酸化物中のScの一部が遊離して金属スカ
ンジウムとなり、電子放出物質内全体に分布するため、
電子放出物質の導電性を高め、中間層による導電性の低
下を補う作用をする。
In addition, some of the Sc in the double oxide is liberated and becomes metallic scandium, which is distributed throughout the electron-emitting material.
It increases the conductivity of the electron-emitting material and compensates for the decrease in conductivity caused by the intermediate layer.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

発明者等が、アルカリ土類金属酸化物層内に酸化スカン
ジウム粉末を分散して含有する上記従来の技術による電
子管陰極の9産試験を行ったところ、電子放出特性を安
定させるエージングに非常に長時間を要し、且つ電子放
出特性が不均一であるという問題があることが判った。
The inventors conducted nine production tests on an electron tube cathode using the above conventional technology containing scandium oxide powder dispersed in an alkaline earth metal oxide layer, and found that it had a very long aging time to stabilize the electron emission characteristics. It has been found that there are problems in that it takes time and the electron emission characteristics are non-uniform.

本発明は、上記従来の技術の問題点を解決し、エージン
グ時間が短くて済み、初期電子放出特性が安定し、製品
間の均一性に富む電子管陰極および其の製造方法を提供
することを目的とする。
SUMMARY OF THE INVENTION An object of the present invention is to solve the above-mentioned problems of the conventional technology, and to provide an electron tube cathode and its manufacturing method that requires short aging time, has stable initial electron emission characteristics, and is highly uniform between products. shall be.

〔問題点を解決するための手段〕[Means for solving problems]

上記問題点を解決するために本発明においては、ニッケ
ル基体金属表面に、バリウムを含むアルカリ土類金属酸
化物層が形成されている電子管陰極において、アルカリ
土類金属酸化物層に、予め別に調製しておいたBa、5
C40,7FA末を0.1〜20重9%一様に分散させ
て含ませることにした。
In order to solve the above problems, in the present invention, in an electron tube cathode in which an alkaline earth metal oxide layer containing barium is formed on the surface of a nickel base metal, the alkaline earth metal oxide layer is prepared separately in advance. Ba, 5
C40,7FA powder was uniformly dispersed and included at 0.1 to 20% by weight.

BaヨSC4O9は、炭酸バリウムと酸化スカンジウム
の混合粉末を非還元性雰囲気中で、1000〜1200
℃で15〜30時間加熱することにより合成することが
出来る。
BayoSC4O9 is made by heating a mixed powder of barium carbonate and scandium oxide to 1000 to 1200 in a non-reducing atmosphere.
It can be synthesized by heating at ℃ for 15 to 30 hours.

また、従来から、いわゆる酸化物陰極を実際に製造する
際には、公知の如(、大気中でも安定なアルカリ土類金
属の炭酸塩を使用しているが、本発明に係る電子管陰極
の製造に際しても、予め合成しておいたB a 3 S
 C4O9粉末を、アルカリ土類全屈炭酸塩粉末に混合
して一様に分散させた後、この混合物を基体金属の表面
に層状に被着させ、加熱分解して、一様に分散したBa
3Sc4O9粉末を含有するアルカリ土類金属酸化物層
に変化させて使用する。
Furthermore, conventionally, when actually manufacturing so-called oxide cathodes, carbonates of alkaline earth metals, which are stable even in the atmosphere, have been used, but when manufacturing the electron tube cathode according to the present invention, Also, B a 3 S synthesized in advance
After C4O9 powder is mixed with alkaline earth carbonate powder and dispersed uniformly, this mixture is deposited in a layer on the surface of the base metal and thermally decomposed to form uniformly dispersed Ba.
It is used by changing to an alkaline earth metal oxide layer containing 3Sc4O9 powder.

〔作用〕[Effect]

あらかじめ、炭酸バリウム(反応時には既に酸化バリウ
ムに変化している)と酸化スカンジウムを混合して加熱
し十分時間をかけて反応生成させたB a35 C4O
9を、アルカリ土類金属酸化物層に分散、添加しである
為、従来の方法に比し、Ba3Sc4O9が電子放出物
質内に均一に存在し、初期から均一性の高い安定した電
子放出特性が得られる。即ち、アルカリ土類金属炭酸塩
に、直接、酸化スカンジウム5cz03粉末の形で添加
して電子管陰極を形成する従来の場合には、エージング
や其の後の動作中に、酸化スカンジウムとアルカリ土類
金属酸化物層が反応するため、酸化物層に変化を生じ、
かつ安定化して良好な電子放出が得られるまでに長時間
を要するものと思われる。
Barium carbonate (already converted to barium oxide at the time of reaction) and scandium oxide are mixed in advance, heated, and reacted for a sufficient amount of time to produce B a35 C4O.
Since Ba3Sc4O9 is dispersed and added to the alkaline earth metal oxide layer, compared to conventional methods, Ba3Sc4O9 is uniformly present in the electron emitting material, resulting in highly uniform and stable electron emission characteristics from the beginning. can get. That is, in the conventional case where an electron tube cathode is formed by directly adding scandium oxide 5cz03 powder to an alkaline earth metal carbonate, scandium oxide and the alkaline earth metal are added during aging or subsequent operation. Because the oxide layer reacts, a change occurs in the oxide layer,
Moreover, it seems that it takes a long time to stabilize and obtain good electron emission.

なお、炭酸バリウムと酸化スカンジウムとの反応生成物
としては、それらの混合比によって、上記Ba3Sc4
0yの他に、Ba2Sc2O5、B a S C204
も得ることでき、何れも電子放出特性を改善する効果を
有するが、これら反応生成物の中で、Ba3Sc4Oq
を添加した場合に最良の電子放出特性改善効果が得られ
ることが認められた。
Note that the reaction product of barium carbonate and scandium oxide may vary depending on their mixing ratio, such as the above-mentioned Ba3Sc4.
In addition to 0y, Ba2Sc2O5, B a S C204
can also be obtained, and all of them have the effect of improving the electron emission characteristics, but among these reaction products, Ba3Sc4Oq
It was found that the best effect of improving electron emission characteristics was obtained when .

このとき、反応生成によって得られたBa3Sc4O+
7中に僅かな量のBazSczOg1BaScz04.
或いは未反応のSC20mが残存していても、効果には
影1なかった。
At this time, Ba3Sc4O+ obtained by reaction production
A small amount of BazSczOg1BaScz04.
Alternatively, even if unreacted SC20m remained, there was no effect at all.

〔実施例〕〔Example〕

以下本発明の一実施例を説明する。炭酸バリウムと酸化
スカンジウムの粉末をモル比で3=2に混合し、大気中
1000〜1200’Cで15〜30時間の熱処理を行
うとBa3Sc4O9が生成される。このバリウムスカ
ンデートを、バリウム、カルシウム、ストロンチウムの
三元炭酸塩粉末に5重量%添加して混合し、これにニト
ロセルローズラッカー酢酸ブチルを加えてローリング混
合して懸濁液をm製した。
An embodiment of the present invention will be described below. When barium carbonate and scandium oxide powders are mixed in a molar ratio of 3=2 and heat treated in the atmosphere at 1000 to 1200'C for 15 to 30 hours, Ba3Sc4O9 is produced. This barium scandate was added in an amount of 5% by weight to ternary carbonate powder of barium, calcium, and strontium and mixed, and to this was added nitrocellulose lacquer butyl acetate and mixed by rolling to prepare a suspension.

この懸濁液を基体金属面上にスプレィ法により、約80
IImの厚さに塗布し、真空排気工程でヒータにより加
熱し炭酸塩から酸化物に分解、更に900〜1100℃
に加熱して安定した電子放出特性が得られるように活性
化工程を施した陰極を製作した。
This suspension was sprayed onto the base metal surface for approximately 80 minutes.
It is coated to a thickness of IIm, heated with a heater during the vacuum evacuation process to decompose the carbonate into oxides, and further heated to 900 to 1100°C.
We fabricated a cathode that underwent an activation process to obtain stable electron emission characteristics when heated.

上記のようにして製作した陰極を使用して、2極管にし
て試験したところ、陰極の動作温度700〜800℃で
1〜2 A / ctAの電子放出特性が得られ、また
多数の陰極を製作して試験を行ったが良好な均一性が認
められた。
When the cathode manufactured as described above was used in a diode tube and tested, an electron emission characteristic of 1 to 2 A/ctA was obtained at a cathode operating temperature of 700 to 800°C, and a large number of cathodes were tested. It was manufactured and tested, and good uniformity was observed.

第1図は本発明の一実施例を示し、図中、1は陰極スリ
ーブ、2はニッケル基体、3は本発明に係る電子放出物
質、4は加熱用ヒータである。
FIG. 1 shows an embodiment of the present invention, in which 1 is a cathode sleeve, 2 is a nickel base, 3 is an electron-emitting material according to the present invention, and 4 is a heater.

第2図は、この陰極を陰極線管に実装し、ヒータ電圧を
定格の11ozにして動作させたときの電子放出の時間
的変化を示す。図中1は本発明による陰極、2はBa3
Sc4O9を添加しなかった陰極の場合である。この図
から明らかなように、電子放出物質層にBa3Sc40
gを分散させることによって良好な電子放出特性を長期
間にわたって維持することが出来る。
FIG. 2 shows the temporal change in electron emission when this cathode is mounted in a cathode ray tube and operated at the rated heater voltage of 11 oz. In the figure, 1 is the cathode according to the present invention, 2 is Ba3
This is the case of a cathode to which Sc4O9 was not added. As is clear from this figure, Ba3Sc40 is used in the electron emitting material layer.
By dispersing g, good electron emission characteristics can be maintained for a long period of time.

なお、上記実施例では、Ba3Sc4O9粉末を5重量
%添加したが、Ba3Sc40gの添加量を0.IM量
%以下にすると効果が少なく実用的でなく、他方、添加
量を20重9%以上にすると初期特性が悪くなって実用
的でない。
In the above example, 5% by weight of Ba3Sc4O9 powder was added, but the amount of Ba3Sc40g added was reduced to 0.5% by weight. When the amount of IM is less than 1%, the effect is small and it is not practical. On the other hand, when the amount added is more than 20% by weight, the initial characteristics deteriorate and it is not practical.

〔発明の効果〕〔Effect of the invention〕

以上説明したように本発明によれば、エージング時間が
短くて済み、初期特性が良く、高い電流密度で長寿命力
5得られ、しかも均一性良好な電子管陰極が製造できる
As explained above, according to the present invention, it is possible to manufacture an electron tube cathode that requires only a short aging time, has good initial characteristics, has a long life with high current density, and has good uniformity.

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

第1図は本発明の一実施例図、第2図は本発明による陰
極の電子放出特性の経時変化を示す図である。 l・−・陰極スリーブ、 2−ニッケル基体、 3・−
本発明に係る電子放出物質、 4−ヒニク。 代理人 弁理士 小川 勝馬  : 〆 1・・・陰極スリーブ 2・・・ニッケル基体 3・・・電子放出物質 4・・・ヒーター 動作時間  (単位二千時間)
FIG. 1 is a diagram showing an example of the present invention, and FIG. 2 is a diagram showing changes over time in the electron emission characteristics of the cathode according to the present invention. l・-・Cathode sleeve, 2-Nickel base, 3・-
Electron-emitting substance according to the present invention, 4-hinik. Representative Patent Attorney Katsuma Ogawa: 1... Cathode sleeve 2... Nickel base 3... Electron emitting material 4... Heater operating time (unit: 2,000 hours)

Claims (1)

【特許請求の範囲】 1、ニッケル基体金属面上に、バリウムを含むアルカリ
土類金属酸化物層が形成されている電子管陰極において
、アルカリ土類金属酸化物層に、Ba_3Sc_4O_
9粉末が分散して含まれていることを特徴とする電子管
陰極。 2、Ba_3Sc_4O_9粉末の含有量を0.1〜2
0重量%とした特許請求の範囲第1項記載の電子管陰極
。 3、予め合成しておいたBa_3Sc_4O_9を、バ
リウムを含むアルカリ土類金属の炭酸塩粉末に混合して
一様に分散させた後、この混合物を基体金属表面に層状
に被着させ、加熱分解して、一様に分散したBa_3S
s_4O_9粉末を含有するアルカリ土類金属酸化物層
を形成することを特徴とする電子管陰極の製造方法。 4、炭酸バリウムと酸化スカンジウムの混合粉末を非還
元性雰囲気中で加熱することによって、Ba_3Sc_
4O_9を合成する特許請求の範囲第3項記載の電子管
陰極の製造方法。
[Claims] 1. In an electron tube cathode in which an alkaline earth metal oxide layer containing barium is formed on a nickel base metal surface, Ba_3Sc_4O_
An electron tube cathode characterized by containing 9 powder dispersed therein. 2. The content of Ba_3Sc_4O_9 powder is 0.1 to 2.
The electron tube cathode according to claim 1, wherein the content is 0% by weight. 3. Mix Ba_3Sc_4O_9 synthesized in advance with barium-containing alkaline earth metal carbonate powder and disperse it uniformly, then apply this mixture to the base metal surface in a layer and heat decompose it. , uniformly dispersed Ba_3S
A method for manufacturing an electron tube cathode, comprising forming an alkaline earth metal oxide layer containing s_4O_9 powder. 4. By heating a mixed powder of barium carbonate and scandium oxide in a non-reducing atmosphere, Ba_3Sc_
The method for manufacturing an electron tube cathode according to claim 3, which comprises synthesizing 4O_9.
JP62259695A 1987-10-16 1987-10-16 Cathode of electron tube and its manufacture Pending JPH01102829A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62259695A JPH01102829A (en) 1987-10-16 1987-10-16 Cathode of electron tube and its manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62259695A JPH01102829A (en) 1987-10-16 1987-10-16 Cathode of electron tube and its manufacture

Publications (1)

Publication Number Publication Date
JPH01102829A true JPH01102829A (en) 1989-04-20

Family

ID=17337640

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62259695A Pending JPH01102829A (en) 1987-10-16 1987-10-16 Cathode of electron tube and its manufacture

Country Status (1)

Country Link
JP (1) JPH01102829A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5121027A (en) * 1990-08-18 1992-06-09 Samsung Electron Devices Co., Ltd. Oxide-coated cathode for CRT and manufacturing method thereof
WO2011040326A1 (en) * 2009-09-29 2011-04-07 電気化学工業株式会社 Rod for electron source, electron source, and electronic appliance

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5121027A (en) * 1990-08-18 1992-06-09 Samsung Electron Devices Co., Ltd. Oxide-coated cathode for CRT and manufacturing method thereof
WO2011040326A1 (en) * 2009-09-29 2011-04-07 電気化学工業株式会社 Rod for electron source, electron source, and electronic appliance
JP2011076753A (en) * 2009-09-29 2011-04-14 Denki Kagaku Kogyo Kk Electron source and electronic equipment

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