JPS6394530A - Filamentary hot cathode - Google Patents
Filamentary hot cathodeInfo
- Publication number
- JPS6394530A JPS6394530A JP61239561A JP23956186A JPS6394530A JP S6394530 A JPS6394530 A JP S6394530A JP 61239561 A JP61239561 A JP 61239561A JP 23956186 A JP23956186 A JP 23956186A JP S6394530 A JPS6394530 A JP S6394530A
- Authority
- JP
- Japan
- Prior art keywords
- emission current
- cathode
- earth metal
- electron emitting
- metal oxide
- 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
- 229910052751 metal Inorganic materials 0.000 claims abstract description 8
- 239000002184 metal Substances 0.000 claims abstract description 8
- 229910001404 rare earth metal oxide Inorganic materials 0.000 claims abstract description 7
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 5
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims abstract description 3
- 239000000463 material Substances 0.000 claims description 7
- 239000000126 substance Substances 0.000 abstract description 7
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical group [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052721 tungsten Inorganic materials 0.000 abstract description 4
- 239000010937 tungsten Substances 0.000 abstract description 4
- 229910052750 molybdenum Inorganic materials 0.000 abstract description 2
- 229910052715 tantalum Inorganic materials 0.000 abstract description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 abstract 1
- 239000011733 molybdenum Substances 0.000 abstract 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 13
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 9
- 239000011575 calcium Substances 0.000 description 7
- 229910052788 barium Inorganic materials 0.000 description 4
- 238000004070 electrodeposition Methods 0.000 description 4
- 238000010894 electron beam technology Methods 0.000 description 4
- 229910052712 strontium Inorganic materials 0.000 description 4
- 229910052791 calcium Inorganic materials 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 238000009125 cardiac resynchronization therapy Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910007541 Zn O Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J1/00—Details of electrodes, of magnetic control means, of screens, or of the mounting or spacing thereof, common to two or more basic types of discharge tubes or lamps
- H01J1/02—Main electrodes
- H01J1/13—Solid thermionic cathodes
- H01J1/14—Solid thermionic cathodes characterised by the material
- H01J1/142—Solid thermionic cathodes characterised by the material with alkaline-earth metal oxides, or such oxides used in conjunction with reducing agents, as an emissive material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J1/00—Details of electrodes, of magnetic control means, of screens, or of the mounting or spacing thereof, common to two or more basic types of discharge tubes or lamps
- H01J1/02—Main electrodes
- H01J1/13—Solid thermionic cathodes
- H01J1/14—Solid thermionic cathodes characterised by the material
- H01J1/144—Solid thermionic cathodes characterised by the material with other metal oxides as an emissive material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J1/00—Details of electrodes, of magnetic control means, of screens, or of the mounting or spacing thereof, common to two or more basic types of discharge tubes or lamps
- H01J1/02—Main electrodes
- H01J1/13—Solid thermionic cathodes
- H01J1/15—Cathodes heated directly by an electric current
Landscapes
- Cathode-Ray Tubes And Fluorescent Screens For Display (AREA)
- Electrodes For Cathode-Ray Tubes (AREA)
- Solid Thermionic Cathode (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は、真空管、CRT、 蛍光表示管等に使用す
る線状熱陰極に関するものである。[Detailed Description of the Invention] [Industrial Application Field] This invention relates to a linear hot cathode used in vacuum tubes, CRTs, fluorescent display tubes, etc.
第2図は例えば特開昭60−84744号公報に示され
た熱陰極をマトリックス状に配置し、通電加熱による電
子放出させる従来の平板型表示装置を示す断面図であり
。図において、(1)はガラス板、セラミック板等で構
成された絶縁性基板、(2)はこの基板(1)上に設け
られた係止部で陰極ワイヤー(3)を係止するための突
起またはリブより成り、その材質は通常金属体で構成さ
れている。陰極ワイヤー(3)は直径10μm程度のタ
ングステン線等の耐熱性金属線が用いられ、その表面に
は酸化物の電子放射物質を保持してなる陰極(4b)が
形成されている。陰極ワイヤー(3)の上方には各陰極
(4b)に対応して貫通孔(8)が設けられたグリッド
電極(7)が設けられ、このグリッド電極(7)の上方
にはさらに上記各陰極(4b)に対応した位置に蛍光体
(9)が塗布されたアノード叫が設けられている。FIG. 2 is a sectional view showing a conventional flat panel display device disclosed in, for example, Japanese Patent Laid-Open No. 60-84744, in which hot cathodes are arranged in a matrix and electrons are emitted by heating with electricity. In the figure, (1) is an insulating substrate made of a glass plate, a ceramic plate, etc., and (2) is a locking part provided on this substrate (1) for locking the cathode wire (3). It consists of protrusions or ribs, and its material is usually metal. The cathode wire (3) is a heat-resistant metal wire such as a tungsten wire with a diameter of about 10 μm, and a cathode (4b) holding an oxide electron emitting substance is formed on the surface of the wire. Above the cathode wire (3), there is provided a grid electrode (7) in which a through hole (8) is provided corresponding to each cathode (4b), and above this grid electrode (7), each cathode is further provided. An anode coated with phosphor (9) is provided at a position corresponding to (4b).
次に動作について説明する。陰極ワイヤー(3)の両端
に電源(図示せず)から電力を供給して約700℃に加
熱すると陰極(4b)表面から電子放射が得られ、グリ
ッドWj 掻(7]及びアノード叫に正の電極を印加す
ることによって、電子ビームは蛍光体(9)を励起する
とともにアノードα■に達する。また、制御1FIl電
極(6)は電子ビームの放射を制御するための電極であ
って、通常負の電圧を印加すると陰極からの電子放射を
停止させることができる。従って、制御電極(6)に正
のパルス電極を印加することにより電子ビームの放射を
制御できる。Next, the operation will be explained. When power is supplied from a power source (not shown) to both ends of the cathode wire (3) and heated to approximately 700°C, electron emission is obtained from the surface of the cathode (4b), and positive radiation is generated in the grid Wj (7) and the anode cry. By applying the electrode, the electron beam excites the phosphor (9) and reaches the anode α■.The control 1FIl electrode (6) is an electrode for controlling the emission of the electron beam, and is usually a negative Electron emission from the cathode can be stopped by applying a voltage of . Therefore, by applying a positive pulse electrode to the control electrode (6), emission of the electron beam can be controlled.
ここで、1ljE極(4b)にはタングステン線からな
る陰極ワイヤー(3)の表面に電着法あるいは塗布法な
どによねバリウム、ストロンチウム、カルシウムの三元
炭酸塩[(Ba、S rp Ca)COJ)が保持され
、表示装置容器内を真空に排気する工程において加熱分
解されて、上記炭酸塩が酸化物〔(Ba、Sr、Ca)
OJに変えられる。そして、陰極ワイヤー(3)のタン
グステンがBaoItil元して、金属上の過剰Baを
生成し、この過剰Baが所謂n型半導体構造を形成し、
陰極(4b)表面の仕事関数を低下させ、エミッシpン
に寄与する。Here, ternary carbonate of barium, strontium, and calcium [(Ba, S rp Ca) COJ is added to the 1ljE electrode (4b) by electrodeposition or coating on the surface of the cathode wire (3) made of tungsten wire. ) is retained and thermally decomposed in the step of evacuating the inside of the display device container, and the carbonate is converted into oxides [(Ba, Sr, Ca)
Can be changed to O.J. Then, the tungsten of the cathode wire (3) converts into BaoItil and generates excess Ba on the metal, and this excess Ba forms a so-called n-type semiconductor structure.
It lowers the work function of the cathode (4b) surface and contributes to emission p.
従来の線状熱陰極は不純ガスの影響によるエミッション
低下が大きいため、上記炭酸塩から酸化物に変える工程
、あるいは表示装置の初期動作時に蛍光体(9)及び係
止部(2)などからの不純ガス放出により、初期エミッ
ション電流が低く、また長時間動作後のBaの消耗が多
く、エミッション電流の低下が大きいなどの問題点があ
った。Conventional linear hot cathodes suffer from a large drop in emissions due to the influence of impure gases. There were problems such as a low initial emission current due to the release of impurity gas, and a large amount of Ba consumed after long-term operation, resulting in a large drop in the emission current.
この発明は上記のような問題点を解消するためになされ
たもので、初期エミッション電流が高く、しかも長時間
動作後のエミッション電流低下の少ない線状熱゛陰極を
得ることを目的とする。The present invention was made to solve the above-mentioned problems, and an object of the present invention is to obtain a linear hot cathode which has a high initial emission current and which exhibits a small drop in emission current after long-term operation.
この発明に係る線状熱陰極は線状の耐熱性金属表面に0
.2〜20重量%の希土類金属酸化物と残部が少なくと
も酸化バリウムを含むアルカリ土類金属酸化物との混合
物とからなる電子放射物質を保持したものである。The linear hot cathode according to this invention has zero
.. It holds an electron emitting material consisting of a mixture of 2 to 20% by weight of a rare earth metal oxide and the balance being a mixture of an alkaline earth metal oxide containing at least barium oxide.
この発明における線状熱陰極は電子放射物質中の希土類
金属酸化物により電子放射物質の活性化が十分に行われ
、かつ不純物の陰極表面での作用を抑制ずろ効果を有す
るので初期エミッション電流が高く、長時間動作後のエ
ミッション低下が減少する。The linear hot cathode of this invention has a high initial emission current because the rare earth metal oxide in the electron emitting material sufficiently activates the electron emitting material, and has the effect of suppressing the action of impurities on the cathode surface. , the emission drop after long-term operation is reduced.
第1図はこの発明の一実施例による線状熱陰極を用いた
表示装置の要部を示す拡大図である。この実施例におい
て陰極(4a)以外の構成は第2図に示す従来のものと
同様である。FIG. 1 is an enlarged view showing the main parts of a display device using a linear hot cathode according to an embodiment of the present invention. In this embodiment, the structure other than the cathode (4a) is the same as the conventional one shown in FIG.
まず・種々の5c2(CO3)よ含有率の電着液を作成
し、従来と同様の電着法に基づき、従来とはゾ同一の膜
厚(8μ)で電子放射物質層を保持した夫々の陰極(4
&)を作成し、これを表示装置の排気工程において加熱
し、(B a、 S r、 Ca)GO,−3c 、
(C03)3を(Ba、Sr、Ca)O−3c、OJに
変えた種々の陰極(4a)を有する表示装置を作成した
。First, electrodeposition solutions with various 5c2 (CO3) contents were prepared, and based on the same electrodeposition method as before, each electrodeposition solution was prepared with an electron-emitting material layer at the same thickness (8μ) as before. Cathode (4
&) and heated in the exhaust process of the display device to form (Ba, S r, Ca)GO, -3c,
Display devices having various cathodes (4a) in which (C03)3 was replaced with (Ba, Sr, Ca)O-3c, OJ were created.
この表示装置完成2時間役の動作時間におけるフィラメ
ントTi流を一定にした時のパルスエミッション電流値
を測定し、その結果を第3図に示す。The pulse emission current value was measured when the filament Ti flow was kept constant during the 2-hour operating time of this display device, and the results are shown in FIG.
この図において横軸はB a O−S r O−Ca
O−8C10J中のScユO,の混合比(重量%)を示
し、縦軸は従来品のパルスエミッション電流値を100
とした時の相対電流値を示した。図から明らかなように
、S c、OJ合比が0.2重量%以上であればエミッ
ション電流の増加傾向が顕著になり、特に混合比1%以
上で高いエミッション電流が得られた。なお、上記混合
比が20重量%を越えろと陰極ワイヤー(3)からの電
子放射物質の脱離が生じ、実用上支障があった。In this figure, the horizontal axis is B a O-S r O-Ca
It shows the mixing ratio (wt%) of ScUO in O-8C10J, and the vertical axis shows the pulse emission current value of the conventional product at 100%.
The relative current value when As is clear from the figure, when the S c and OJ combined ratio is 0.2% by weight or more, the emission current tends to increase significantly, and especially when the mixture ratio is 1% or more, a high emission current is obtained. Incidentally, if the above-mentioned mixing ratio exceeds 20% by weight, the electron emitting substance will be desorbed from the cathode wire (3), which poses a practical problem.
次にこの発明に基づきScユ0,5重量%を含む電子放
射物質を保持した陰極と従来の(Ba、Sr。Next, based on the present invention, a cathode containing an electron emitting material containing 0.5% by weight of Sc and a conventional cathode (Ba, Sr).
Ca)Oからなる電子放射物質を保持した陰極を各々配
設した2種類の表示装置を作成した。陰極以外は全て同
一条件である。蛍光体層には低速電子線用蛍光体(Zn
O: Zn)を用い、パターンは直径が4.Ommの円
形パターンを数個配設したものを用いた。Two types of display devices were created, each having a cathode holding an electron-emitting substance made of Ca)O. All conditions were the same except for the cathode. The phosphor layer contains a phosphor for low-speed electron beams (Zn
O: Zn) was used, and the pattern had a diameter of 4. A pattern with several Omm circular patterns was used.
従来品と実施例の2種類に関して、フィラメント電圧、
アノード電圧及びグリッド電圧を同一条件で各々5本づ
つ点灯動作させ蛍光体層の輝度を測定し、その平均値の
相対値(従来品の動作2時間における平均輝度を100
とした)を第4図にプロットシた。さらに、輝度測定と
平行して第3図に示したパルスエミッション電流と同一
条件で各々の動作時間におけるパルスエミッション電流
値を測定し、その平均値の相対値(従来品の動作2時間
におけろ平均輝度を100とした)も第4図に併せてプ
ロットした。上記実施例の動作2時間の初期輝度は従来
品に比べ18%高い値を示した。この図から明らかなよ
うに動作初期から1000時間の長時間動作にわたって
輝度及びエミッション電流の双方において、実施例が優
れた特性を有している。特に従来品が動作数100時間
後の輝度、パルスエミッション電流の低下が大きいのに
比べ、実施例の効果は顕著である。動作時間1000時
間後の蛍光体層をX線マイクロアナライザーで分析した
ところ、従来品の場合は実施例に比べ多量のBaが検出
されたことから、実施例の浸れた特性は動作中のBaの
消耗が少ないことによると考えられろ。このように、初
期輝度が高(動作後の残存輝度も高いので、表示装置が
明るい所でも使用可能になるなどの効果をも有する。Regarding the two types, the conventional product and the example, the filament voltage,
The brightness of the phosphor layer was measured by lighting five lamps each under the same anode voltage and grid voltage conditions, and the relative value of the average value (the average brightness of the conventional product for 2 hours of operation was 100
) is plotted in Figure 4. In addition, in parallel with the brightness measurement, the pulse emission current value was measured at each operating time under the same conditions as the pulse emission current shown in Figure 3, and the relative value of the average value (compared to the conventional product for 2 hours of operation) was measured. The average brightness was set as 100) and was also plotted in FIG. The initial brightness of the above example after two hours of operation was 18% higher than that of the conventional product. As is clear from this figure, the example has excellent characteristics in both brightness and emission current over a long period of 1000 hours from the initial stage of operation. In particular, compared to the conventional product, which exhibits large reductions in brightness and pulse emission current after 100 hours of operation, the effects of the embodiment are remarkable. When the phosphor layer was analyzed using an X-ray microanalyzer after 1000 hours of operation, a larger amount of Ba was detected in the conventional product compared to the example, so the immersion characteristics of the example reflect the presence of Ba during operation. This is probably due to less wear and tear. In this way, since the initial brightness is high (and the residual brightness after operation is also high), the display device can be used even in bright places.
このようなこの発明の顕著な効果の原因は明確にはなっ
ていないが、以下のように考えられる。Although the cause of such remarkable effects of the present invention is not clear, it is thought to be as follows.
従来の陰極においては、陰極ワイヤー(3)のタングス
テンとの反応で還元されたBaは拡散等により、陰極表
面へ移動しBad、SrO,CaOの表面に吸着し表面
の仕事関数を低下させる。一方、この発明を実施してな
る陰極においては、5020.3上に吸着したBaが何
らかの理由でエミッションを増加させる効果と動作中の
Baの消耗を抑制する効果を有すると考えられる。In the conventional cathode, Ba reduced by the reaction with tungsten of the cathode wire (3) moves to the cathode surface by diffusion or the like and is adsorbed on the surfaces of Bad, SrO, and CaO, reducing the work function of the surface. On the other hand, in the cathode according to the present invention, Ba adsorbed on 5020.3 is considered to have the effect of increasing emissions for some reason and the effect of suppressing Ba consumption during operation.
以上、この発明の効果をScよ03を実施例に説明した
が、ScユOJ以外の希土類金属酸化物でも上記効果が
得られる。Although the effects of the present invention have been explained using Sc03 as an example, the above effects can also be obtained with rare earth metal oxides other than Sc00J.
また、綿状耐熱性金属もタングステンに限定されず、主
成分がMo、Ta、Ptなどの場合も同様の効果が得ら
れる。陰極の形状は実施例の如き直線状に限らず、板状
、コイル状、スパイラル状など任意の線状陰極形状で上
記した効果は丸られろ。上記した効果は蛍光表示管、線
状熱陰極を用いたCRT、電子題徹鏡、蛍光ランプの高
性能化に寄与することは明白である。また、陰極ワイヤ
ー(3)に流れろ電流値を増加させて高輝度化を実現す
る場合には、特に寿命特性の向上に顕著な効果を有する
。Further, the cotton-like heat-resistant metal is not limited to tungsten, and similar effects can be obtained even when the main component is Mo, Ta, Pt, etc. The shape of the cathode is not limited to the linear shape as in the embodiment, but any linear cathode shape such as a plate shape, a coil shape, a spiral shape, etc. can achieve the above-mentioned effects. It is clear that the above effects contribute to higher performance of fluorescent display tubes, CRTs using linear hot cathodes, electronic telescopes, and fluorescent lamps. In addition, when increasing the current value flowing through the cathode wire (3) to achieve high brightness, it has a particularly remarkable effect on improving life characteristics.
以上説明したようにこの発明の陰極は初期エミッション
電流が多く、かつエミッション電流の動作中の維持が優
れているので表示装置の高輝度化、電子管装置などの高
性能化を実現する効果がある。As explained above, the cathode of the present invention has a large initial emission current and is excellent in maintaining the emission current during operation, so it is effective in realizing higher brightness of display devices and higher performance of electron tube devices.
第1図は、この発明を実施してなる表示装置の断面図、
第2図は従来の表示装置を示す断面図、第3図はScユ
03の混合比とパルスエミッション電流との関係を示す
特性図、第4図は表示装置の動作時間と輝度及びパルス
エミッション電流との関係を示す特性図である。
(1)は絶縁性基板、(2)は陰極ワイヤー、(4&)
は陰極、(9)は蛍光体層、QO)はアノードである。
なお、各図中、同一符号は同−又は相当部分を示す。FIG. 1 is a sectional view of a display device implementing the present invention;
Fig. 2 is a cross-sectional view showing a conventional display device, Fig. 3 is a characteristic diagram showing the relationship between the mixing ratio of ScU03 and pulse emission current, and Fig. 4 is an operating time, brightness, and pulse emission current of the display device. FIG. (1) is an insulating substrate, (2) is a cathode wire, (4&)
is a cathode, (9) is a phosphor layer, and QO) is an anode. In each figure, the same reference numerals indicate the same or corresponding parts.
Claims (1)
属酸化物と残部が少なくとも酸化バリウムを含むアルカ
リ土類金属酸化物との混合物とからなる電子放射物質を
保持したことを特徴とする線状熱陰極。It is characterized by holding an electron-emitting material consisting of a mixture of 0.2 to 20% by weight of rare earth metal oxide and alkaline earth metal oxide containing at least barium oxide on the surface of the linear heat-resistant metal. linear hot cathode.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23956186A JP2599910B2 (en) | 1986-10-07 | 1986-10-07 | Linear oxide cathode for cathode ray tubes |
KR1019870007380A KR910001397B1 (en) | 1986-10-07 | 1987-07-09 | Hot cathode in wire form |
US07/105,668 US4897574A (en) | 1986-10-07 | 1987-10-05 | Hot cathode in wire form |
DE3780246T DE3780246T3 (en) | 1986-10-07 | 1987-10-06 | Wire-shaped hot cathode. |
EP87114566A EP0263483B2 (en) | 1986-10-07 | 1987-10-06 | Hot cathode in wire form |
CA000548815A CA1276965C (en) | 1986-10-07 | 1987-10-07 | Hot cathode in wire form coated with rare and alkaline earth metal oxides containing barium oxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23956186A JP2599910B2 (en) | 1986-10-07 | 1986-10-07 | Linear oxide cathode for cathode ray tubes |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6394530A true JPS6394530A (en) | 1988-04-25 |
JP2599910B2 JP2599910B2 (en) | 1997-04-16 |
Family
ID=17046631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23956186A Expired - Lifetime JP2599910B2 (en) | 1986-10-07 | 1986-10-07 | Linear oxide cathode for cathode ray tubes |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP2599910B2 (en) |
KR (1) | KR910001397B1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0366633U (en) * | 1989-10-27 | 1991-06-28 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4833677A (en) * | 1971-09-03 | 1973-05-11 | ||
JPS4912758A (en) * | 1972-05-12 | 1974-02-04 | ||
JPS6084744A (en) * | 1983-10-15 | 1985-05-14 | Matsushita Electric Ind Co Ltd | Hot cathode |
-
1986
- 1986-10-07 JP JP23956186A patent/JP2599910B2/en not_active Expired - Lifetime
-
1987
- 1987-07-09 KR KR1019870007380A patent/KR910001397B1/en not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4833677A (en) * | 1971-09-03 | 1973-05-11 | ||
JPS4912758A (en) * | 1972-05-12 | 1974-02-04 | ||
JPS6084744A (en) * | 1983-10-15 | 1985-05-14 | Matsushita Electric Ind Co Ltd | Hot cathode |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0366633U (en) * | 1989-10-27 | 1991-06-28 |
Also Published As
Publication number | Publication date |
---|---|
KR910001397B1 (en) | 1991-03-04 |
JP2599910B2 (en) | 1997-04-16 |
KR880005646A (en) | 1988-06-29 |
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