JPS6047360A - Low pressure mercury vapor discharge lamp - Google Patents

Low pressure mercury vapor discharge lamp

Info

Publication number
JPS6047360A
JPS6047360A JP15592983A JP15592983A JPS6047360A JP S6047360 A JPS6047360 A JP S6047360A JP 15592983 A JP15592983 A JP 15592983A JP 15592983 A JP15592983 A JP 15592983A JP S6047360 A JPS6047360 A JP S6047360A
Authority
JP
Japan
Prior art keywords
oxide
filament
emitter
tungsten
metal
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
JP15592983A
Other languages
Japanese (ja)
Inventor
Tetsuo Mine
峯 哲郎
Yoshimi Watanabe
渡辺 好美
Shigehiro Sato
佐藤 滋洋
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.)
Toshiba Corp
Original Assignee
Toshiba 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 Toshiba Corp filed Critical Toshiba Corp
Priority to JP15592983A priority Critical patent/JPS6047360A/en
Publication of JPS6047360A publication Critical patent/JPS6047360A/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
    • H01J61/0675Main electrodes for low-pressure discharge lamps characterised by the material of the electrode
    • H01J61/0677Main electrodes for low-pressure discharge lamps characterised by the material of the electrode characterised by the electron emissive material

Landscapes

  • Discharge Lamp (AREA)

Abstract

PURPOSE:To obtain a low pressure mercury vapor discharge lamp scarcely suffering from blackening during a long period of lighting, by adding an activating metal to an alkaline earth metal oxide of an emitter, with which a filament is coated. CONSTITUTION:A coil filament 6 made of molybdenum is coated with a substance, in which a stiffening material 8 and an activating metal 9 are added to an emitter 7 composed of a ternary oxide of barium, strontium and calcium. Said stiffening material 8 is powder of the oxide having a high melting point such as tungsten oxide, zirconia and titanium oxide while having a function of protecting the emitter from an impact of electrons and ions. The activating metal 9 consists of powder of tungsten and zirconium while having a function of gradually reducing barium oxide at high temperature for generating a very small amount of free barium long and continuously. The filament 6 has a coated layer 10 of a composition Ba3MoO6 on its metal surface.

Description

【発明の詳細な説明】[Detailed description of the invention]

「う′α明の技術分野〕 本発明はモリブデン製コイルフィラメントを封装した低
圧水銀蒸気放電灯に関する。 〔発明の技術的背景とその問題点〕 螢光ランプなどの低圧水銀蒸気放電灯はバルブの両端に
タングステンフィラメントにエミッタを被后してなる゛
覗極を封装しである。このような111極においCは、
動作時フィラメントのタングステンが高温になってエミ
ッタの酸化物たとえばBa1lに作用し、次の反応によ
って遊離バリウムを生じてこのバリウムから電子放射を
行なうものである。 tiB++o + W = Ba3WO6+ 3B+し
かして、タングステンはその還元力が適当で、適当ノf
速1徒でかつ継続的に作用するため、Baの生成に、1
.・^不足がなく、長期間にわたり、有効に作動するの
である。 しかしながら、タングステンは加工性が非常に悪く、こ
れに伴なう焼鈍処理も1500℃以上の高温を必要とし
、さらにコイル成形には高温なモリブデン製マンドレル
を使用し、しかも成形後1:このマンドレルを溶解して
除去している。このような理由によって、タングステン
フィラメントは非常に1+;b41jであるばかりか資
源的にも問題がある。 これに対し、タングステンの代りにモリブデンでフィラ
メントを構成することが考えられた。たしかに、モリブ
デンフィラメントは加工性が良く、しかモ鉄マンドレル
が使用できるため、安価に製造でき5資源的にも問題が
少ない。 しかしながら、モリブデンフィラメントを使用し−Cμ
ると放電灯の管端部が早1iJl (二点化して使用に
耐えないことが判明した。従東、この原因とし−C、モ
リブデンの化学的活性が強いため、酸化’lkの1ζ〉
元が過度に進行し、バリウムなどが過)電に発生してこ
れが飛11(シて黒化するものと考えられ、その対策が
留望されていた、 〔発明の目的〕 本発明)Jモリブデンフィラメントを使用し、しかも良
好に動作し、民期点灯しても黒化の少ない低用水銀蒸気
放′屯灯を提供することを目的とする。 〔発明の()・′L要〕 フィラメント(二被着したエミッタのアルカリにヵ1金
11JK 酸化物C二付活金属を添加したことによつC
、フィラメントのエミッタ付活性能が失われても添加し
た付活金174によってエミッションを行なわ1上るも
のである。 〔発明の実施例〕 本発明者らは研究の結果、:、μ化の原因が1−、ミッ
タの過刺還元ではないことを発1″LL、た。研究にL
れば、ランプ製造の過程において、エミッタの活性化す
7t、わちアルカリ土類金jt≦炭酸塩を熱分解して酸
化!1・’<Jに変成する工程があるが、この活性化(
二当も)フィラメント表面において次の反応(二よって
フィラメントの金属の錯化合物を生じる。 3]1aC+13 +M−+Ba 3M06 +3CO
(M : Na金1m)しかして、タングステンフィラ
メントにおいてはタング;(テンの化学活性が小さいた
めI:l a B WO6の生成/)−少なく、ランプ
構成後の動作において、酸化バリウムの還元に支障がな
い。モリブデンはこれに反し、化学的活性が大きいため
大i11のB a3 M 。 Ooを生成してフィラメントの金属表面を彼粗し、この
ためモリブデン金属と酸化バリウムとの反応を1ilJ
害[2て遊離バリウム生成を減少させる。この結果、エ
ミッションが低下して111極電圧が負側(二増犬・「
るためイオンi4134によってエミッタが飛散し−C
県期黒化の原因になることが判明した。そこで、本づ1
)明者らはフィラメントのモリブデン金属に依存するこ
となく酸化バリウムを還元できるようにJ−Jlはエミ
ッションに支障がなく、早期黒化のおビれがなくなるこ
とに想到し、エミッタにタングステンなどの付活金hA
を添加することにしたのである。 131下、本発明の詳細を図示の実施例によ−)て説明
する。1χ1は本発明を適用してなる螢光ランプの一例
を承り31図中、(1)は直’t?形ガラスバルブ、(
2)はこのバルブ(1)内筒に形成されたり、2光休被
膜、f:l)。 (、()はバルブ(1)の両端を閉塞したステム、(4
)、(4)はこのステム(3)l(3)からバルブ(1
)内に尋人した1 エlの4.(入線、(H−H) 、
 (!5)はこれら占、1入線(4)、(4)間;−装
「°iしたフィラメント′電極である。そして、バルブ
(1)内仁アルゴンなどの始動ガスとども(二逼t 4
1)の水◇1.!がロムされている。 」−配達、極(5)は第2図に示すように、モリブデン
X1・9コイルフイラメント(6)にバリウム・スト[
lンテウム・カルシウムの三元酸化物からなるエミン5
I(7)に浦強(二4(0で示す。)(8)、(8)お
よび付活金1.+((〕で示す。、) (9) 、 f
9)を添加して被着してj・、る、。 これら袖5!1!4A(8)は酸化タンゲス1ン、酸化
ジルlニウム、酸化チタンなど旨融点の酸化物の粉末−
(゛、エミッタを゛重子やイオンの衝撃から保護する作
Jlを有4−る。」二記付活金屈(9)はタングステン
、ジルコニウノ・などの粉末からなり高’/MAにおい
て酸化パリウl−4・徐々C二還元して微性の有離バリ
ウムを長Jυ目j:跨続1..て生成する作用を有する
。なお、フィラメント(1;)はその金Iiハ表面にB
 a3 IV4 +106なる組成のfJk +SJ層
(10)シイ1する。 っYじ、このランプの製造方法を説明する。定Irg 
4 () w螢光ランプ用モリブデン製2車コイ/Lフ
ィラノント((1)をステム(3)に絹゛線する。−万
、バリヴノ・・ストロンチウム・カルシウムの三元炭酸
塩4・71 末に111′シ化ジルコニウノ、粉末およ
び上記炭酸塩粉末にk・1
Technical Field of the Invention The present invention relates to a low-pressure mercury vapor discharge lamp sealed with a molybdenum coil filament. [Technical background of the invention and its problems] Low-pressure mercury vapor discharge lamps such as fluorescent lamps are A viewing pole consisting of a tungsten filament and an emitter is sealed at both ends.In such a 111 pole, C is
During operation, the tungsten of the filament becomes hot and acts on the oxide of the emitter, for example Ba1l, and the next reaction produces free barium, which emits electrons. tiB++o + W = Ba3WO6+ 3B+ However, tungsten has an appropriate reducing power and an appropriate nof
Since it acts rapidly and continuously, 1 is required for the production of Ba.
..・^There is no shortage and it operates effectively for a long period of time. However, tungsten has very poor workability, and the accompanying annealing process requires a high temperature of 1,500°C or higher.Furthermore, a high-temperature molybdenum mandrel is used for coil forming. It is dissolved and removed. For these reasons, tungsten filaments are not only extremely 1+; b41j but also problematic in terms of resources. In response, it has been considered to construct the filament from molybdenum instead of tungsten. It is true that molybdenum filaments have good workability and can be manufactured using molybdenum iron mandrels, so they can be manufactured at low cost and have fewer problems in terms of resources. However, using molybdenum filaments -Cμ
It was found that the tube end of the discharge lamp quickly became 1iJl (2 points) and was unusable. Juto attributed this to the strong chemical activity of -C and molybdenum, which led to oxidation of 1ζ of 'lk'.
It is thought that the molybdenum progresses excessively and barium etc. are generated due to overcurrent, which causes blackening, and a countermeasure against this problem has been desired. To provide a low-use mercury vapor emission lamp that uses a filament, operates well, and exhibits little blackening even when lit for civilian use. [Required ()・'L of the invention] Filament (2) C by adding 11JK oxide C2 activated metal to the alkali of the deposited emitter
Even if the filament loses its emitter activating ability, the added activated gold 174 performs emission and increases the number by 1. [Embodiment of the Invention] As a result of our research, the present inventors found that the cause of μ-ization was not 1-, Mitter's over-piercing reduction.
Then, in the lamp manufacturing process, the emitter is activated by 7t, which means that alkaline earth gold jt≦carbonate is thermally decomposed and oxidized! There is a process of metamorphosis into 1・'<J, but this activation (
2) The following reaction occurs on the surface of the filament (2), thereby producing a complex compound of the metal of the filament. 3] 1aC+13 +M-+Ba 3M06 +3CO
(M: 1 m of Na gold) However, in a tungsten filament, tung; (because the chemical activity of ten is small, I: la B WO6 formation/) is small, and in operation after the lamp is constructed, it interferes with the reduction of barium oxide. There is no. Molybdenum, on the other hand, has a large i11 B a3 M due to its high chemical activity. The reaction between molybdenum metal and barium oxide is reduced by generating Oo to roughen the metal surface of the filament.
[2] Reduces free barium production. As a result, the emission decreases and the 111 pole voltage is on the negative side (two-in-one, "
The emitter is scattered by ion i4134 and -C
It has been found that this is the cause of prefectural blackening. So, book 1
) In order to reduce barium oxide without relying on the molybdenum metal of the filament, the researchers realized that J-Jl has no problem with emission and eliminates the cracks caused by early blackening, so they used materials such as tungsten in the emitter. Activation money hA
I decided to add . 131, details of the invention will be explained by means of illustrated embodiments. 1χ1 is an example of a fluorescent lamp to which the present invention is applied. In Figure 31, (1) is direct? shaped glass bulb, (
2) The inner cylinder of this bulb (1) is formed with a 2-photoresist coating, f:l). (, () is the stem with both ends of the valve (1) closed, (4
), (4) are from this stem (3) l (3) to the valve (1
) 1. El. 4. (Incoming line, (H-H),
(!5) is the filament electrode between these two input wires (4) and (4); 4
1) Water◇1. ! is ROMed. ”-Delivery, the pole (5) is made of barium strut [6] on a molybdenum
Emine 5 consisting of ternary oxide of lntheum and calcium
I (7) has Ura Qiang (24 (indicated by 0)) (8), (8) and activation money 1. + (indicated by ()) (9), f
9) is added and deposited. These sleeves 5!1!4A (8) are powders of oxides with a high melting point, such as tanges oxide, zirnium oxide, and titanium oxide.
(It has a function to protect the emitter from the bombardment of molecules and ions.) The activated metal (9) is made of powders such as tungsten and zirconium, and is made of powders such as tungsten and zirconia. -4.It has the effect of gradually reducing C2 to generate minute free barium by long Jυth j: straddling 1.. The filament (1;) has B on the surface of the gold Ii.
a3 IV4 +SJ layer (10) with a composition of +106. Now, I will explain how to manufacture this lamp. Fixed Irg
4 (2) Two molybdenum coils for fluorescent lamps/L filanont (wire (1) to the stem (3).-10,000, Valivno...Ternary carbonate of strontium and calcium 4.71 At the end 111' zirconium silicide, powder and the above carbonate powder k・1

【3車b;%に当るタングス
デン金1+j’i粉末を?水加12、これを酢酸ブチル
に混η1し−Cスラリにして上記フィラメント(6)に
塗布する。そして、このマウ、・トステムを螢光ランプ
r= x:It込み、排気しながらフィラメント(6)
に通′屯して発熱させ、その熱によ一部て炭rib塩を
分解して酸化物に要]チする。このと1寸、残留空気お
よび発生し、た酸化性ガスの作用に、1つてタングステ
ン金hjスの一部は酸化されて補強i、、I’ (8)
になるが、一部は金にのまま残留して付活金属(9)に
なる。、また、この活性化の過程においてフィラメント
(6)の表面はモリブデンと炭酸用とが反応してなる1
3a、J1o06なる組成の被覆層(Illiで(々キ
1〕される その仮、】lj常の方法Cランプに41・
11′成・1″る。 つぎに、この栓1ン光ランプの作用を説明ず/)。S′
−のランプな点灯すると、’rK極(5)は′電子やイ
レンの/+f[1人によって高/111aに熱せ1うれ
る。しかしながら。 フィラメント(6)はその表面をBa3Mo06など錯
化)1物の被キΩ層110)で覆われているので酸化物
を工:、すしJ−る作用が弱いやしかし、イ(1活金属
(9)はタングステンで4’i’4 Ifされているの
で被膜がほとんどなく、1゜たがって従来のタングステ
ンフィラメントど同様金1ijj (9)の表面(=お
いてエミソタイど除々に還元し′(微量の遊離バリウム
を生成し、・二のバリウノ・か1・良好(二電子を放射
する。したか−)で、この放′t、’(L灯は電極のエ
ミッションが良好で、陰極’7Jq圧が低く、したがっ
て、イオン側法が弱いのでスパッタが712なく、早期
黒化のおそれがない。 つぎに、上述のように形成した40W螢光ランプを1、
]/、ll金jt4(9)をイ]しないものおよびマメ
11来のタングヌデ)・フィラメントを有するものと比
較して本発明の7・、h果を実1つ・η1.た。この結
果を次表に示す。 こ())ジ、か1っコ゛ミッタにイ・]活合金A’:を
7,1(加したものはイ、11占・、i′属のないもの
に比較1−て性能が大幅に向」ニしtI’(= ;l−
のタングステンフィラメントのランプと同4:’Iiな
・1〕1能が得ら、!1だ。 な13、本発明において付活金属はタングステン、ジル
J−ウムのほかチタンやハフニウムなどでもよく、拶“
はエミッタ酸化物を適当な辻IWで還元して」いtJl
 ’J+′定して;1・lj 、j」、1.の遊シjl
バリ1ツムを生成すればよい、、 にだ、付/1も金1
7t5の形状や大ぎさは粉末に限らず、籾−いν1さと
反応性とを考慮して定めればよい。 また、本発明は螢光ランプのほか殺菌灯7f、どにOj
M用してNG’t ’lcりh果をイJするものである
。 〔発明のクシ1県〕 Δパ、l〜明の低圧水釧蒸気放j1工灯はモリブデンフ
ィラノニ/ト(ニネ皮イら゛する二[ミッタ(二このエ
ミッタをJl、〈元t、て7f;:子を放射させるイー
1活金属を添加したのC、フィラメント表it+iがモ
リブデン6ハ化合物で披裂、゛5れC(=I活作用を失
った場合でも付活金11域が有効にエミッタを還元して
電子、放射を行なわ(するので、長1・」1にわたり安
定して動作し、1昇期黒化のおそAしがない
[3 car b; % of tungsten gold 1 + j'i powder? Add water 12 and mix this with butyl acetate to make a -C slurry and apply it to the filament (6). Then, attach the fluorescent lamp r=
The carbon salt is partially decomposed into oxides by the heat generated. At this point, due to the action of the residual air and the generated oxidizing gas, a part of the tungsten gold metal is oxidized and reinforced i,,I' (8)
However, a part remains as gold and becomes an activated metal (9). In addition, during this activation process, the surface of the filament (6) becomes 1, which is formed by the reaction of molybdenum and carbonic acid.
3a, a coating layer with a composition of J1o06 (Illi).
11' and 1''.Next, I will not explain the function of this one-light lamp/).S'
When the - lamp is lit, the 'rK pole (5) is heated to high /111a by electrons and electrons /+f[1]. however. The surface of the filament (6) is covered with a layer 110) of a complexed active metal (such as Ba3Mo06), so the effect of processing the oxide is weak. 9) is made of 4'i'4 If with tungsten, so there is almost no coating, and therefore, as with conventional tungsten filaments, the surface of gold 1ijj (9) is gradually reduced at the emisotai' (a trace amount). It generates free barium, and the emission is good (it emits two electrons), and the emission of the electrode is good, and the cathode'7Jq pressure is Therefore, since the ion side method is weak, there is no spatter and there is no risk of early blackening.Next, a 40W fluorescent lamp formed as described above was heated to
]/, ll gold jt4(9) and those with filaments, compared to those with filaments, the present invention's 7., h fruit with one fruit, η1. Ta. The results are shown in the table below. The performance of the active alloy A': 7,1 (added to the transmitter is significantly improved compared to the one without group I'). "NishitI'(=;l-
Same as the tungsten filament lamp of 4: 'Ii na・1] 1 power is obtained,! It's 1. 13. In the present invention, the activated metal may be tungsten, dillium, titanium, hafnium, etc.
reduce the emitter oxide with a suitable Tsuji IW.
'J+'determined;1・lj,j'', 1. The play city jl
All you have to do is generate 1 Tsum, Nida, Attached/1 also has 1 Gold.
The shape and size of 7t5 are not limited to powder, and may be determined by taking into consideration the grain size ν1 and reactivity. In addition to fluorescent lamps, the present invention also applies to germicidal lamps,
It's a way to get rid of NG't'lch results by using M. [1 prefecture of the invention] ΔP, l~Ming's low-pressure water steam discharge j1 Industrial lights are made of molybdenum filanonitrate (nine skin). 7f;: C, the filament surface it+i is split with a molybdenum 6 compound, and the activated metal 11 area becomes effective even when the active effect is lost. The emitter is reduced to emit electrons (therefore, it operates stably over a long period of 1.1 years, and there is no risk of blackening during the 1 period.

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

第1図は本発明の低圧水銀蒸−″λi放電灯の一実+1
’i!i例の14j1面図、第2図は同じく要部拡大断
面図である。 (1)−・・バルブ (2)・・・螢光体肢膜(5)・
・・フィラメント電44 (fil ・−フィラメン)
F’7+・・・エミッタ(8)・・・袖強拐(9)・・
・伺活金属 代1シリ人 弁理士 井 上 −男 第 1 図 34 lz 、tJ 第 2 図
Figure 1 shows an example of the low-pressure mercury evaporation lamp of the present invention +1
'i! 14j of Example i and FIG. 2 are enlarged cross-sectional views of the main parts. (1) --- Bulb (2) -- Fluorescent limb membrane (5)
・・Filament electric 44 (fil ・-filamen)
F'7+...Emitter (8)...Sleeve kidnapping (9)...
・Kikkatsu Metal Fee: 1 shillin Patent Attorney Inoue - Male 1st Figure 34 lz, tJ Figure 2

Claims (1)

【特許請求の範囲】[Claims] バルブと、このバルブの端部に封装されたモリブデン製
コイルフィラメントと、このフィラメント(二被着され
たエミッタとを具備し、上記−にミッタ目アルカリ土類
金属酸化物にこの酸化物な還カCして′電子を放射させ
る付活金属ケ添加して/、(ることを特徴とする低圧水
銀蒸気放電灯。
It comprises a bulb, a molybdenum coiled filament sealed at the end of the bulb, and an emitter attached to the filament, in which a reducing force of the oxide is applied to an alkaline earth metal oxide in the emitter. A low-pressure mercury vapor discharge lamp characterized by adding an activated metal for emitting electrons.
JP15592983A 1983-08-26 1983-08-26 Low pressure mercury vapor discharge lamp Pending JPS6047360A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15592983A JPS6047360A (en) 1983-08-26 1983-08-26 Low pressure mercury vapor discharge lamp

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15592983A JPS6047360A (en) 1983-08-26 1983-08-26 Low pressure mercury vapor discharge lamp

Publications (1)

Publication Number Publication Date
JPS6047360A true JPS6047360A (en) 1985-03-14

Family

ID=15616595

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15592983A Pending JPS6047360A (en) 1983-08-26 1983-08-26 Low pressure mercury vapor discharge lamp

Country Status (1)

Country Link
JP (1) JPS6047360A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102103975A (en) * 2009-12-21 2011-06-22 陈宗烈 Lamp cathode structure and gas discharge lamp adopting same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102103975A (en) * 2009-12-21 2011-06-22 陈宗烈 Lamp cathode structure and gas discharge lamp adopting same

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