JPS5975553A - Electrode for discharge lamp - Google Patents

Electrode for discharge lamp

Info

Publication number
JPS5975553A
JPS5975553A JP18575782A JP18575782A JPS5975553A JP S5975553 A JPS5975553 A JP S5975553A JP 18575782 A JP18575782 A JP 18575782A JP 18575782 A JP18575782 A JP 18575782A JP S5975553 A JPS5975553 A JP S5975553A
Authority
JP
Japan
Prior art keywords
electron
barium
electrode
radiating material
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.)
Pending
Application number
JP18575782A
Other languages
Japanese (ja)
Inventor
Keiji Watabe
渡部 勁二
Keiji Fukuyama
福山 敬二
Masato Saito
正人 斉藤
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.)
Mitsubishi Electric Corp
Original Assignee
Mitsubishi Electric Corp
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 Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP18575782A priority Critical patent/JPS5975553A/en
Publication of JPS5975553A publication Critical patent/JPS5975553A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00Gas-discharge or vapour-discharge lamps
    • H01J61/02Details
    • H01J61/04Electrodes; Screens; Shields
    • H01J61/06Main electrodes
    • H01J61/067Main electrodes for low-pressure discharge lamps

Landscapes

  • Discharge Lamp (AREA)

Abstract

PURPOSE:To improve electron radiation capabilities by containing 0.05-5wt% of extremely fine powders of at least one of nickel, iron, and cobalt in an electron radiating material containing an alkaline earth metal including at least barium. CONSTITUTION:Argon and mercury is sealed in a discharge tube 1 made of glass, electrodes 2a, 2b are arranged on both sides of the discharge tube 1, and the glass inside of the discharge tube 1 is coated with a phosphor 3. Tungsten coils are coated with an electron radiating material made by mixing 0.05-5wt% of extremely fine powders of at least one of nickel, iron, and cobalt to an electron radiating material containing an alkaline earth metal including at least barium to form the electrodes 2a, 2b. Thereby, the conductivity of the electron radiating material is increased and the adhesiveness to the electrode can be improved. As a result, a discharge lamp electrode excellent in electron radiation capabilities can be produced.

Description

【発明の詳細な説明】 この発明は、放゛亀灯に設置された電極に塗布される電
子放射物質にIAするものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention applies IA to an electron emitting material applied to an electrode installed in a radiation lamp.

この放電灯の例とし、て螢光ランプの構造を第1図に示
す。ガラス製の放電y+it内にはアルゴンおよび水銀
が封入され、敢電管山の両端には電極(2a)(2b)
が設定され、また放電管(11のガラス円曲には螢光体
(3)が箆布されている。
As an example of this discharge lamp, the structure of a fluorescent lamp is shown in FIG. Argon and mercury are sealed inside the glass discharge y+it, and electrodes (2a) (2b) are placed at both ends of the tube.
is set, and a phosphor (3) is installed in the glass curve of the discharge tube (11).

従来、けい光ランプの電憾としてはタングステンのコイ
ルにバリタム、ストロンチウムおよびカルシウムの炭ハ
塩には化ジルコニウム′(il−疹加した電子放射物質
が塗布され、上記炭酸基はランプ製造工程中でカロ熱さ
れて酸化バリウムなどの酸化物に分解される。この従来
の電子放射物質はランプ点灯時電極基体であるタングス
テンにより還元され、酸化バリウム(Bad)は 6BaO+ W−+Ba3WO6+ JBaの反応によ
りバリウム(Ba) i生成する。このバリウムは′屯
憾の゛由;子放躬に寄与するが、その一部は放電草間に
飛散して看壁に付盾し、その量が多いと管1’ll、i
黒化を生ずる。この管S’111f黒化金抑JilJす
るために上記物質中に酸化ジルコニウムが函加されてい
る。これにより管端黒化の夙少は見られるが。
Traditionally, fluorescent lamps are made by coating a tungsten coil with an electron-emitting substance containing baritum, strontium, and calcium carbonate salts, and adding zirconium chloride to the carbonate group during the lamp manufacturing process. It is calorically heated and decomposed into oxides such as barium oxide.This conventional electron-emitting material is reduced by tungsten, which is the electrode base, when the lamp is turned on, and barium oxide (Bad) is converted to barium (Bad) by the reaction of 6BaO+ W-+Ba3WO6+ JBa. Ba) i is produced. This barium contributes to the release of children, but some of it is scattered between the discharge plants and attached to the wall, and if the amount is large, ,i
Causes blackening. Zirconium oxide is boxed in the above material to suppress the blackened gold in this tube S'111f. As a result, the blackening of the tube end is slightly reduced.

十分ではない。これは、酸化ジルコニウムの両力Uによ
ってBaの飛散は少なく抑えられたが、ランプ点灯時間
の経過とともに順化バリウムと酸化ジルコ= f)ムが
反応してバリウム、ジルコンI[ff1(Ba Zr 
Oa ) k形成し、そのため塗布膜の尋箪性が低下し
、そのため′厄子放側龍が低下し、′電極からの飛散が
増えて、やはり冒壁黒化につながる。
Not enough. This is because the scattering of Ba was suppressed to a small extent by the dual force U of zirconium oxide, but as the lamp lighting time elapsed, the acclimatized barium and zirconium oxide = f) reacted, and barium and zircon I [ff1 (Ba Zr
Oa)k is formed, and as a result, the ductility of the coating film decreases, and as a result, the ``repellency'' decreases, and ``scattering from the electrode increases, which also leads to blackening of the surface.

この冗明はこのような従来の欠点に誂みてなされたもの
であり、電子放射物質にニッケル、鉄。
This clarification was made in response to the drawbacks of the conventional method, and the electron-emitting materials used were nickel and iron.

コバルトの超微粉末の少なくとも1種’i 0.05〜
5重量%混会させたことによって、電子放射物質の接着
性および導電性を艮くし′g端黒化の少ない放電灯用電
極を提供するものである。
At least one type of ultrafine cobalt powder'i 0.05~
By incorporating 5% by weight of the electron emitting material, the adhesiveness and conductivity of the electron emitting material are improved, and an electrode for a discharge lamp with less edge blackening is provided.

以下にこの発明の実施例と従来例とを説明すると、まず
従来例として、酸化バリウム(BaO)55:&魚チ、
酸化ストロンチウム(SrO)28i輩チおよび酸化カ
ルシウム(Cab)13虚童チの三元酸化物に酸化ジル
コニウム(Zr02)4重′jjL%を含有した電子放
射物質を有するけい光ランプ用1JL極全備えた40W
けい光ランプを作成した。なお、上記′−極は8通常、
バリウム、ストロンチウムおよびカルシウムの炭w 閂
tc w化ジルコニウムを混合し、こn紫ニトロセルロ
ーズラッカーとともに匪ハブチルに入れ、ボールミルを
行なって懸濁液とし、これtタングステンの二重コイル
もL(は三重コイルに塗イドし、排気工程において加熱
分解を行なうことによって侮られる。上記従来の40W
けい元ランプの点灯試捩全行なったところ3000時間
点灯後の光束維持率は85%でおった。
Examples of the present invention and conventional examples will be explained below. First, as a conventional example, barium oxide (BaO) 55: & fish chi,
1JL complete set for fluorescent lamps with electron emitting material containing strontium oxide (SrO) 28i and calcium oxide (Cab) ternary oxides and zirconium oxide (Zr02) 4x'jjL% 40W
Created a fluorescent lamp. Note that the above '-pole is usually 8,
Barium, strontium, and calcium charcoal zirconium chloride are mixed together, put into a nitrocellulose lacquer together with this purple nitrocellulose lacquer, and ball milled to form a suspension. The above conventional 40W
When the lighting test of the source lamp was completed, the luminous flux maintenance rate after 3000 hours of lighting was 85%.

次にこの発明の詳細な説明すると、酸化バリウム(Ba
d)約55m:It%、酸化ストロンチウム(SrO)
約28重証係および酸化カルシウム(Cab)約ll上
優の三元酸化物と酸化ジルコニウム(Z r Oz )
約4N量チ全官有した′帆子放別物質に300大の平均
粒蚤のニッケル粉末を各棟の蚤で添加した′1子放痢物
質を有する一潅全備えた40W0い光ランプ点灯中し、
上記従来例と同僚に点灯試1沃葡行なった。
Next, to explain this invention in detail, barium oxide (Ba
d) Approximately 55m: It%, strontium oxide (SrO)
Approximately 28 times the ternary oxide and calcium oxide (Cab) and zirconium oxide (ZrOz)
Approximately 4N amount of ``one-leaf excretion substance'' which is made by adding nickel powder of 300 average grains of fleas to each government-owned ``flea release substance'' in each house.A 40W light lamp is lit. Inside,
I conducted a lighting test using the conventional example above and a colleague.

その結果を次表に示す。The results are shown in the table below.

この表から、従来のBad、 SrO,Cab、 Zr
O2からなる電子放射物質音用いた螢光ランプに比べて
、実施例2〜4に示す′電子放射物質を用いた螢光ラン
プの光束維持率は優れていることがわかる。
From this table, conventional Bad, SrO, Cab, Zr
It can be seen that the fluorescent lamps using the electron emitting material shown in Examples 2 to 4 have superior luminous flux maintenance rates as compared to the fluorescent lamps using the electron emitting material made of O2.

このように実施例のものの光束維持率が優れているのは
下記の理由によると推定される。すなわち、前記した従
来の電子放射物質においては。
The reason why the luminous flux maintenance factor of the example is excellent as described above is presumed to be due to the following reason. That is, in the conventional electron emitting material described above.

ZrO□1dBaoと電極基体のタングステンとの反応
全抑制し、 Baの生成全制御する。この結果、 Ba
の放電苗量への飛散は減少する。
The reaction between ZrO□1dBao and tungsten of the electrode base is completely suppressed, and the production of Ba is completely controlled. As a result, Ba
Dispersion to the amount of discharged seedlings is reduced.

しかしながら+  BhOとZrO□が反応してBaZ
rO3をノ1〉成し、七のため軍子放射物質傾布膜の尋
箪性が低下し、−f:のため電子放射能が低下し、電極
からの電子放射物質の飛散が増えて、やはり管壁黒化V
(つながる。
However, +BhO and ZrO□ react to form BaZ
rO3 is formed, the stability of the military radioactive substance gradient film decreases due to 7, the electron radioactivity decreases due to -f, and the scattering of electron emissive substances from the electrode increases, As expected, tube wall blackening V
(Connect.

これに対してこの発明の′電子放射物質は、 Niの微
粉末k R’i加したことに特徴がある。Ni倣粉末の
添加により、電子放射物質顔布族の得策性が同上すると
ともに、′電極基体との接着性がよくなるので、ランプ
点灯中のBaの生成が安定し、電子放射詫が良好に保た
れるのでf&への成畝が減少する。
On the other hand, the electron emitting material of the present invention is characterized by the addition of fine Ni powder kR'i. The addition of Ni imitation powder not only improves the effectiveness of the electron emitting material, but also improves its adhesion to the electrode substrate, which stabilizes Ba production during lamp lighting and maintains electron emission well. Because it sag, the growth ridges to f& are reduced.

混合するニッケル粉末の量は、0.05〜5重祉チが望
ましい。上記量が0.05重iii%未満になると・N
1粉末の尋?JE剤としての効果が小さく、上記量が5
重量%’を越えると、yuH1末の表面酸化の影響で電
子放射能が低下する。
The amount of nickel powder to be mixed is preferably 0.05 to 5%. When the above amount is less than 0.05% by weight, N
1 powder fathom? The effect as a JE agent is small, and the above amount is 5
If it exceeds % by weight, the electron radioactivity decreases due to surface oxidation of the yuH1 powder.

上記実加例においては、ニッケルの超微初末會使用した
例を示したが、鉄あるいはコバルトのU床?用いても同
体の効果が得られるものであシ。
In the above practical application example, an example was shown in which an ultrafine nickel powder was used, but is it iron or cobalt U-bed? Even when used, the same effect can be obtained.

またこれらの粉末の半均粒蚤け0.2ミクロン以下であ
れはよい。
It is also acceptable if the semi-uniform grain size of these powders is 0.2 microns or less.

また土id、 X施汐0ではBaO* 8rO+ Ca
O* ZrO2からなる電子放射物質について示したが
、この発明はこれにとどまるものでな(、BaO−8r
O,HaO−CaO−B & O、B a2 (、’、
 a WO6、B 1k1−B Srg 、2 CaW
06など種々のBaを含む′「電子放射物質に歯用でき
るものでめる。
Also, at soil id, X application 0, BaO* 8rO+ Ca
Although the electron emitting material made of O*ZrO2 has been shown, the invention is not limited thereto (
O, HaO-CaO-B & O, B a2 (,',
a WO6, B 1k1-B Srg, 2 CaW
These include various types of Ba-containing materials such as 06 that can be used as electron-emitting materials.

また、上記実hl!+例では螢光ランプについて示した
が、他の放電灯9例えば高圧水銀ランプ、高圧 ・ナト
リウムランプなど柚々に適用できる。
Also, the actual HL above! Although the example shows a fluorescent lamp, it can also be applied to other discharge lamps, such as high-pressure mercury lamps, high-pressure sodium lamps, etc.

以上述べたように、この発明は少なくともバリウム’(
+−宮ひアルカリ土類金)84全含有する電子放射物質
に、ニッケル、鉄、コバルトの超微粉末の少なくとも1
棟を0.115〜5mJt%混曾烙せることにより、電
子放射物質の尋電性會増加し9電極への接漸性全よくす
ることが出来、その結果′電子放創能力のすぐれた放′
市灯用電イ婆會提供するものである。
As mentioned above, this invention is applicable to at least barium'(
+- Miyahi alkaline earth gold) 84 All contained electron emitting substances include at least one of ultrafine powders of nickel, iron, and cobalt.
By mixing the ridge with 0.115 to 5 mJt%, it is possible to increase the electroconductivity of the electron emitting material and improve its contact with the nine electrodes. ′
It is provided by an electric car for city lights.

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

図は螢光ランプの構成をボす図である。 図において(2m)(2b)は′幅悌である。 代理人 葛 !1!7− 他 − The figure shows the configuration of a fluorescent lamp. In the figure, (2m) and (2b) are 'widths. Agent Kuzu! 1!7- Others-

Claims (1)

【特許請求の範囲】[Claims] 少なくともバリウムを含むアルカリ土類金属金言有する
電子放射物質にニッケル、鉄、コバルトの超畝紛木の少
なくとも1棟i 0.05〜51景饅毘合させた電子放
射物質會有することを特徴とする放電灯用゛−1惚。
It is characterized by having an electron emitting material which is made by combining an electron emitting material containing an alkaline earth metal containing at least barium with at least one super-rugged wood of nickel, iron, and cobalt. -1 love for discharge lamps.
JP18575782A 1982-10-22 1982-10-22 Electrode for discharge lamp Pending JPS5975553A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18575782A JPS5975553A (en) 1982-10-22 1982-10-22 Electrode for discharge lamp

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18575782A JPS5975553A (en) 1982-10-22 1982-10-22 Electrode for discharge lamp

Publications (1)

Publication Number Publication Date
JPS5975553A true JPS5975553A (en) 1984-04-28

Family

ID=16176329

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18575782A Pending JPS5975553A (en) 1982-10-22 1982-10-22 Electrode for discharge lamp

Country Status (1)

Country Link
JP (1) JPS5975553A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5847498A (en) * 1994-12-23 1998-12-08 Philips Electronics North America Corporation Multiple layer composite electrodes for discharge lamps
US6383416B1 (en) 1999-03-12 2002-05-07 Tdk Corporation Electron-emitting material and preparing process
US6432325B1 (en) 1999-03-19 2002-08-13 Tdk Corporation Electrode

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5847498A (en) * 1994-12-23 1998-12-08 Philips Electronics North America Corporation Multiple layer composite electrodes for discharge lamps
US6383416B1 (en) 1999-03-12 2002-05-07 Tdk Corporation Electron-emitting material and preparing process
US6432325B1 (en) 1999-03-19 2002-08-13 Tdk Corporation Electrode

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