JPS62193031A - Cathode for electron tube - Google Patents
Cathode for electron tubeInfo
- Publication number
- JPS62193031A JPS62193031A JP61035670A JP3567086A JPS62193031A JP S62193031 A JPS62193031 A JP S62193031A JP 61035670 A JP61035670 A JP 61035670A JP 3567086 A JP3567086 A JP 3567086A JP S62193031 A JPS62193031 A JP S62193031A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- cathode
- alkaline earth
- sintered
- nickel
- 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
Links
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 36
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims abstract description 16
- 239000010953 base metal Substances 0.000 claims abstract description 16
- 239000000843 powder Substances 0.000 claims abstract description 16
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 15
- HYXGAEYDKFCVMU-UHFFFAOYSA-N scandium oxide Chemical compound O=[Sc]O[Sc]=O HYXGAEYDKFCVMU-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052788 barium Inorganic materials 0.000 claims abstract 4
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims abstract 4
- 239000000463 material Substances 0.000 claims description 20
- 238000010438 heat treatment Methods 0.000 abstract description 4
- 239000000725 suspension Substances 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 3
- 239000000126 substance Substances 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 238000001994 activation Methods 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical group [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229910052706 scandium Inorganic materials 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 238000002679 ablation Methods 0.000 description 1
- -1 alkaline earth metal carbonate Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 231100000568 intoxicate Toxicity 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明はディスプレイ用陰極線管などの電子管に用い
られる傍熱形の陰極に関し、特に、その電子放射特性の
向上を図ったものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an indirectly heated cathode used in an electron tube such as a cathode ray tube for a display, and is particularly directed to improving the electron emission characteristics thereof.
従来、この種の陰極には、ニッケルを主成分とする基体
金属上にBaを含むアルカリ土類金属酸化物層を被着形
成した陰極が用いられているが、最近、ディスプレイ用
陰極線管や撮像管の高精細摩化に伴って、+m電流密度
使用する要求が強くなってきている。Conventionally, this type of cathode has been made by depositing an alkaline earth metal oxide layer containing Ba on a base metal mainly composed of nickel. With the high-definition ablation of tubes, there is an increasing demand for using +m current density.
しかしながら、従来の陰極では帆5〜0.8A/am2
の電流密度での使用が限界であり、これ以上の電流密度
で使用すると、陰極の寿命が短くなるという問題が生じ
る。However, with conventional cathodes, the sail 5~0.8A/am2
There is a limit to its use at a current density of 1,000,000,000 yen, and if it is used at a current density higher than this, the problem arises that the life of the cathode will be shortened.
第2図は、ディスプレイ用陰極線管や撮像管に用いられ
ている従来の陰極の構成を示す縦断面図で、fl+はS
i、Mg等の還元性元素を微量含むニッケルからなる基
体金属、(2)は基体金属(11の面上に被着形成さね
ている電子放射物質層で、Ba、 Sr。Figure 2 is a longitudinal cross-sectional view showing the structure of a conventional cathode used in display cathode ray tubes and image pickup tubes, where fl+ is S
i, a base metal made of nickel containing a small amount of reducing elements such as Mg; (2) is an electron emitting material layer deposited and formed on the surface of the base metal (11);
Caの三元アルカリ土類金属酸化物で形成さね遊離Ba
が含まれている。(31け基体金属(11を介して電子
放射物質層(21を加熱するヒータである。アルカリ土
類金属酸化物層(2)は、Ba、 Sr、 Caの複合
炭酸塩粉末をバインダ溶液中に懸濁させた塗布液を、ス
プレなどの方法によって基体金属+l+の面上に塗布し
、真空排気工程においてヒータ(31によって加熱して
炭酸塩から酸化物に変える分解工程と、さらに900〜
1100℃に加熱してその酸化物の一部を還元して酸素
を取り除き、半導体的性質を有するようにする活性化工
程とを捲して電子放射性を得ている。基体金属(11の
中に微量のSi、Mgなどの還元性元素を含有させてい
るのは、活性化工程に訃いて還元反応を行なわせるため
である。すなわち基体金属(lj中の還元性元素は、拡
散によりアルカリ土類金属酸化物と基体金属fi+との
界面に移動してアルカリ土類金属酸化物と反応する。例
えばBaOは以下のように反応する。Free Ba formed in ternary alkaline earth metal oxides of Ca
It is included. (This is a heater that heats the electron emitting material layer (21) through the base metal (11). The suspended coating liquid is applied onto the surface of the base metal +l+ by a method such as spraying, and in the vacuum evacuation step, it is heated by a heater (31) to convert the carbonate into an oxide, and then the decomposition step is performed at 900~
Electron emissivity is obtained by heating to 1100° C. to reduce part of the oxide, remove oxygen, and make it have semiconductor properties. The reason why a trace amount of reducing elements such as Si and Mg is contained in the base metal (11) is to cause a reduction reaction to occur during the activation process. moves to the interface between the alkaline earth metal oxide and the base metal fi+ by diffusion and reacts with the alkaline earth metal oxide.For example, BaO reacts as follows.
2 BaO+Si = 2Ba+5iOzBaO+Mg
= Ba + MgO
この結果、アルカリ土類金属酸化物の一部が還元されて
酸素欠乏型の半導体となり、陰極温度’700〜Boo
℃の動作温度で0.5〜0.8 A/am”の電流密度
で使用できる電子放射物質層(2]が得られる。2 BaO+Si = 2Ba+5iOzBaO+Mg
= Ba + MgO As a result, a part of the alkaline earth metal oxide is reduced to become an oxygen-deficient semiconductor, and the cathode temperature increases from '700 to Boo.
An electron-emissive material layer (2) is obtained which can be used at a current density of 0.5-0.8 A/am'' at an operating temperature of .degree.
従来の陰極が上記以上の電流を取り出すことができない
のけ、
■ 活性化工程における還元反応の結果、基体金属+I
+と電子放射物質層(2)との界面に5i02. Mg
Oなどの酸化物層(中間層)が形成され、この中間層が
高抵抗層となって電流の流ねを妨げる。Although the conventional cathode cannot extract a current higher than the above, ■ As a result of the reduction reaction in the activation process, the base metal + I
5i02. at the interface between + and the electron emitting material layer (2). Mg
An oxide layer (intermediate layer) such as O is formed, and this intermediate layer becomes a high resistance layer and prevents the flow of current.
■ 中間層が存在するために、アルカリ土類金属酸化物
と還元性元素との反応が抑制さねて、十分な情のBaが
生成さねないなどの理由によるものと考えらねる。(2) This is thought to be due to the fact that the presence of the intermediate layer prevents the reaction between the alkaline earth metal oxide and the reducing element from being suppressed, preventing sufficient Ba from being produced.
〔発明が解決しようとする問題点1
以上のように従来の陰極では、活性化工程において、全
屈基体[II七アルカリ土類金属酔化物層(2)の界面
に中間層が生成さねるため、高電流密度で使用できない
という問題点があった。[Problem to be Solved by the Invention 1] As described above, in the conventional cathode, an intermediate layer is not formed at the interface of the fully curved substrate [II hepta-alkaline earth metal intoxicate layer (2)] in the activation process. However, there was a problem in that it could not be used at high current densities.
この発明は上記問題点を解消するためになされたもので
、中間層の存在による高電流の電子放射の抑制及び遊離
Baの生成の抑制による影響が低減でき、高電流密度で
使用できる陰極を得ることを目的とする。This invention was made to solve the above problems, and provides a cathode that can be used at high current densities by reducing the effects of suppressing high current electron emission and suppressing the generation of free Ba due to the presence of the intermediate layer. The purpose is to
この発明に係る陰極は、ニッケA/基体金属北にニッケ
ル粉末焼結層を設け、川にその上にアルカリ土類駿化物
の中に酸化スカンジウム(S0203)粉末を分散して
含有させた電子放射物質層を設番すたものである。The cathode according to this invention has a nickel powder sintered layer on the nickel A/substrate metal, and an electron emitting layer on which scandium oxide (S0203) powder is dispersed in an alkaline earth sulfide. The material layers are numbered.
ニッケル基体上のニッケル粉末焼結層は中間層の形吸、
による導電性の低下を防止し、更に、アルカリ土類金属
酸化物の中に分散している酸化スカンジウム粉末は、電
子放射物質層の導電性を高めるとともに、酸化スカンジ
ウムがアルカリ土類金属酸化物と反応して生成された接
合酸化物、例えばBa5Sc409が、陰極の作動中に
熱分解を起して遊離Baを生成し、熱電子の放射を増大
させる作用を行なう。The nickel powder sintered layer on the nickel substrate forms the middle layer,
In addition, the scandium oxide powder dispersed in the alkaline earth metal oxide increases the conductivity of the electron emitting material layer, and also prevents the scandium oxide from interacting with the alkaline earth metal oxide. The junction oxide produced by the reaction, for example Ba5Sc409, undergoes thermal decomposition during operation of the cathode to produce free Ba, which acts to increase thermionic emission.
以下この発明の一実施例をvJ1図により説明する。 An embodiment of the present invention will be explained below using diagram vJ1.
粒径3〜5ミクロンのニッケル金属粉末ヲ=+−ロセル
ロースラツカ、酢酸ブチル等と混合して懸濁液を作成し
、こわをスプレィによって約30ミクロンの厚さになる
ようにニッケル基体金属+1j上に塗布し、こわを水素
雰囲気中にて1OOO’C、10分間の熱処理を行ない
、上記ニッケル金属粉末の焼結層(41を作成した。ま
た、バリウム、ストロンチウム、カルシウムの三元炭酸
塩粉末に酸化スカンジウム粉末を5.0重量係添加して
混合し、こねにニトロセルロースラッカ、酢酸ブチルを
加えてローリング混合して懸濁液を調製した。この懸濁
液を焼結層(4)上にスプレィ法により約80ミクロン
の厚さに塗布し、従来と同じ条件で排気加熱工程および
活性化工程を施して陰極を製作した。(21は電子放射
物質層で、(2a)/f′iアルカリ土類金属炭酸塩が
熱分解して出来たアルカリ土類金属酸化物、(2b)t
de化スカンジウム粉末である。Mix nickel metal powder with a particle size of 3 to 5 microns with cellulose lacquer, butyl acetate, etc. to create a suspension, and spray the nickel base metal powder to a thickness of about 30 microns. The sintered layer (41) of the above nickel metal powder was prepared by applying heat treatment on the nickel metal powder for 10 minutes at 100'C in a hydrogen atmosphere. 5.0 weight percent of scandium oxide powder was added and mixed, and nitrocellulose lacquer and butyl acetate were added to the mixture and mixed by rolling to prepare a suspension.This suspension was poured onto the sintered layer (4). The cathode was fabricated by applying the coating to a thickness of approximately 80 microns by a spray method and performing an exhaust heating process and an activation process under the same conditions as before. (21 is the electron emitting material layer, (2a)/f'i Alkaline earth metal oxide produced by thermal decomposition of alkaline earth metal carbonate, (2b)t
It is scandium powder.
このようにして製作した陰極を使用して2極真空管を作
成して試験したところ、陰極の動作温度’700〜80
0℃で1〜2A/cm2の電子放射特性が得られ、従来
に比較して高電流密度で長期間使用できることが確認さ
れた。When a diode vacuum tube was made and tested using the cathode manufactured in this way, the operating temperature of the cathode was found to be between '700 and '80.
It was confirmed that an electron emission characteristic of 1 to 2 A/cm2 was obtained at 0°C, and that it could be used for a long period of time at a higher current density than conventional products.
上記実楢例vcふ・いて、良好な電子放射が得られたの
は、つき゛の理由によるものと考えらねる。The reason why good electron emission was obtained in the above practical example VC is considered to be due to the following reasons.
■ 電子放射物質層(21内に添加混合した酸化スカン
ジウム粉末(2b)がアルカリ土類金属酸化物(2a)
例えばBaOと反応して生成された複合酸化物(Bas
Sc<09)が電子放射物質層(2)内に分散しており
、この複合酸化物が陰極の動作中に熱分解を起こして遊
離Baを生成しゃすぐなる。従来の陰極における遊離B
aO生Wは、基体金属(1)中に微量含まねているSl
やMg等の還元性元素による還元反応に依存していたが
、この実捲例においては複合酸化物の熱分解により生成
された遊離Baが付加されるので、たとえ中間層により
還元反応が抑制されていたとしても、遊離Baの量が不
足することがない。■ The scandium oxide powder (2b) added and mixed in the electron emitting material layer (21) is an alkaline earth metal oxide (2a).
For example, a complex oxide (Bas
Sc<09) is dispersed in the electron emitting material layer (2), and this composite oxide prevents thermal decomposition from occurring during operation of the cathode to generate free Ba. Free B in conventional cathode
aO raw W contains a trace amount of Sl in the base metal (1).
However, in this example, free Ba generated by thermal decomposition of the composite oxide is added, so even if the intermediate layer suppresses the reduction reaction. Even if the amount of free Ba is increased, the amount of free Ba will not be insufficient.
■ 複合酸化物中のScの一部が遊離して金属スカンジ
ウムとなり、電子放射物質層(2)内全体に分布する。(2) A part of Sc in the composite oxide is liberated and becomes metallic scandium, which is distributed throughout the electron emitting material layer (2).
この金属スカンジウムの存在により電子放射物質FT+
21の導電性が高まり、中間層による導電性の低下を補
って、電子放射物質層(2)の導電性が向上する。Due to the presence of this metal scandium, the electron emitting material FT+
The conductivity of the electron emitting material layer (2) increases, compensating for the decrease in conductivity due to the intermediate layer, and improves the conductivity of the electron emitting material layer (2).
■ ニッケル粉末による焼結層(41け多孔質となって
おり、この上に塗布さねた電子放射物質層(2)の一部
は上記焼結層(41の中に浸透してニッケル基体金IU
[+1と接触し、この部分において中間層が生吸するが
、大部分の電子放射物質層(21は、焼結層(41と接
触しているため、上記中間層の生成による導電性の低下
を防ぐことができる。■ A sintered layer (41) made of nickel powder is porous, and a part of the electron emitting material layer (2) coated on top of this sintered layer (41) penetrates into the nickel-based gold layer (41). IU
[In contact with +1, the intermediate layer absorbs live in this part, but most of the electron emitting material layer (21 is in contact with the sintered layer (41), so the conductivity decreases due to the formation of the intermediate layer. can be prevented.
なお、ニッケル基体金属(11上に形成するニッケル粉
末焼結層(41の厚みは、10〜50ミクロンが望まし
い。上記厚みが10ミクロン以下であると、中間層がこ
の焼結層(4)を越えて生成さね、十分な効果を発揮し
ない。又、上記厚みが50ミクロンを越えると、アルカ
リ土類金団酸化物の焼結層(41への浸透が十分でな(
なり、ニッケル基体金属(11と接触する割合が少な(
なって陰極の活性化が十分に行なわ相な(なる。The thickness of the nickel powder sintered layer (41) formed on the nickel base metal (11) is preferably 10 to 50 microns. If the thickness is 10 microns or less, the intermediate layer In addition, if the thickness exceeds 50 microns, the alkaline earth metal oxide may not penetrate sufficiently into the sintered layer (41).
, the proportion of contact with the nickel-based metal (11) is small (
This means that the cathode is sufficiently activated.
また、電子放射物質層(21に添力口する酸化スカンジ
ウム粉末については、5.0重量係混合した例を説明し
たが、酸化スカンジウムの混合量が0.1重量係以下で
は効果が小さくて実用的でな(、他方、混合量が20重
量憾以上になると、初期特性が悪ぐなって実用的ではな
かった。Furthermore, regarding the scandium oxide powder added to the electron emitting material layer (21), an example was explained in which a 5.0 weight ratio was mixed, but if the amount of scandium oxide mixed is less than 0.1 weight ratio, the effect is small and it is not practical. On the other hand, when the amount of the mixture exceeds 20% by weight, the initial properties become poor and it is not practical.
以上のようにこの発明は、アルカリ土類金属炭酸塩粉末
に酸化スカンジウム粉末を混合し均一に分散させたもの
を、ニッケル金属粉末の焼結層を備えた基体金属の面上
にwi着させて形成した陰極であるから、電子放射物質
層内に分散させた酸化スカンジウムにより生成されてい
る複合酸化物による遊離Baの生成作用と、電子放射物
質層の導電性を高める作用、並びに焼結層の介在により
中間層の生成による導電性の低下を防ぐ作用により従来
の陰極よりも高電流密度で使用できる電子管陰極か得ら
れる。As described above, the present invention involves depositing a uniformly dispersed mixture of alkaline earth metal carbonate powder and scandium oxide powder on the surface of a base metal provided with a sintered layer of nickel metal powder. Since it is a formed cathode, the action of generating free Ba by the composite oxide produced by scandium oxide dispersed in the electron emitting material layer, the action of increasing the conductivity of the electron emitting material layer, and the action of increasing the conductivity of the sintered layer. The interposition prevents a decrease in conductivity due to the formation of an intermediate layer, resulting in an electron tube cathode that can be used at a higher current density than conventional cathodes.
第11図は本発明の電子管陰極の一例を示す縦断面図、
第2図は従来の電子管陰極を示す縦断面図である。
(11・・・基体金属、(2)・・・電子放射物質層、
(2a)・・・アルカリ土類舎監酸化物、(2b)・・
・酸化スカンジウム粉末、(4)・・・焼結層。
なお1図中、同一符号は同一または相当部分を示す。FIG. 11 is a longitudinal sectional view showing an example of the electron tube cathode of the present invention;
FIG. 2 is a longitudinal sectional view showing a conventional electron tube cathode. (11...Base metal, (2)...Electron emitting material layer,
(2a)...alkaline earth oxide, (2b)...
- Scandium oxide powder, (4)...sintered layer. In addition, in FIG. 1, the same reference numerals indicate the same or corresponding parts.
Claims (1)
厚みで設けられたニツケル粉末の焼結層と、バリウムを
含むアルカリ土類金属酸化物中に酸化スカンジウム粉末
が分散して含まれたものからなり上記焼結層上に被着さ
れた電子放射物質層とを備えた電子管陰極。(1) A sintered layer of nickel powder with a thickness of 10 to 50 microns on the surface of a nickel base metal, and scandium oxide powder dispersed in an alkaline earth metal oxide containing barium. and an electron emissive material layer deposited on the sintered layer.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61035670A JPS62193031A (en) | 1986-02-19 | 1986-02-19 | Cathode for electron tube |
CA000513900A CA1270890A (en) | 1985-07-19 | 1986-07-16 | Cathode for electron tube |
US06/886,777 US4797593A (en) | 1985-07-19 | 1986-07-17 | Cathode for electron tube |
DE86305560T DE3689134T2 (en) | 1985-07-19 | 1986-07-18 | Cathode for electron tube. |
EP86305560A EP0210805B1 (en) | 1985-07-19 | 1986-07-18 | Cathode for electron tube |
CN86104753.2A CN1004452B (en) | 1985-07-19 | 1986-07-18 | Cathod for electric valve |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61035670A JPS62193031A (en) | 1986-02-19 | 1986-02-19 | Cathode for electron tube |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62193031A true JPS62193031A (en) | 1987-08-24 |
JPH0544767B2 JPH0544767B2 (en) | 1993-07-07 |
Family
ID=12448308
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61035670A Granted JPS62193031A (en) | 1985-07-19 | 1986-02-19 | Cathode for electron tube |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62193031A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5122707A (en) * | 1988-02-02 | 1992-06-16 | Mitsubishi Denki Kabushiki Kaisha | Cathode in a cathode ray tube |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58186128A (en) * | 1982-04-22 | 1983-10-31 | Mitsubishi Electric Corp | Electron tube cathode |
JPS58192237A (en) * | 1982-05-07 | 1983-11-09 | Hitachi Ltd | Impregnation type cathode |
-
1986
- 1986-02-19 JP JP61035670A patent/JPS62193031A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58186128A (en) * | 1982-04-22 | 1983-10-31 | Mitsubishi Electric Corp | Electron tube cathode |
JPS58192237A (en) * | 1982-05-07 | 1983-11-09 | Hitachi Ltd | Impregnation type cathode |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5122707A (en) * | 1988-02-02 | 1992-06-16 | Mitsubishi Denki Kabushiki Kaisha | Cathode in a cathode ray tube |
Also Published As
Publication number | Publication date |
---|---|
JPH0544767B2 (en) | 1993-07-07 |
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Legal Events
Date | Code | Title | Description |
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EXPY | Cancellation because of completion of term |