JPS60170151A - Glow starter - Google Patents
Glow starterInfo
- Publication number
- JPS60170151A JPS60170151A JP2503384A JP2503384A JPS60170151A JP S60170151 A JPS60170151 A JP S60170151A JP 2503384 A JP2503384 A JP 2503384A JP 2503384 A JP2503384 A JP 2503384A JP S60170151 A JPS60170151 A JP S60170151A
- Authority
- JP
- Japan
- Prior art keywords
- zirconium
- electron emission
- aging
- glow starter
- electron
- 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
Links
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B41/00—Circuit arrangements or apparatus for igniting or operating discharge lamps
- H05B41/02—Details
- H05B41/04—Starting switches
- H05B41/06—Starting switches thermal only
- H05B41/08—Starting switches thermal only heated by glow discharge
Landscapes
- Discharge Lamp (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の利用分野〕
本発明はZrを主成分とする電子放射性物質を電極に被
着させてなるグロースタータの改良に係り、特に、この
種のグロースタータにおけるエージング時間の短縮化に
関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Application of the Invention] The present invention relates to an improvement in a glow starter in which an electrode is coated with an electron-emitting substance containing Zr as a main component. This is related to the shortening of .
一般のグロースタータより不動作限界電圧(B電圧)と
グロー放電終止電圧(Vend)とを高く設定したグロ
ースタータにおいて、例えばB電圧が80V以上、Ve
ndが75ρ■以上の特性を得るためには電子放射性物
質としてZrメタル粉末を電極に被着させて活性化させ
たものを使用する。In a glow starter whose inoperable limit voltage (B voltage) and glow discharge end voltage (Vend) are set higher than general glow starters, for example, if the B voltage is 80V or more, Ve
In order to obtain a characteristic in which nd is 75 ρ■ or more, a Zr metal powder deposited on the electrode and activated is used as the electron radioactive substance.
しかしながら、バイメタルの最高使用温度の制限から排
気中における活性化のための加熱温度には限界があり、
十分な活性化が出来ず、その結果、起動電圧(Vs)や
Vendを最適値にすることができなかった。そこで、
このような初期特性を得るため、エージングで活性化を
促進させることになるが、その時間は約1時間を要する
ため量産的には工数がかかり過ぎる欠点があった。However, due to restrictions on the maximum operating temperature of bimetals, there is a limit to the heating temperature for activation in the exhaust gas.
Sufficient activation could not be achieved, and as a result, the starting voltage (Vs) and Vend could not be set to optimal values. Therefore,
In order to obtain such initial characteristics, activation is promoted by aging, but this takes about one hour, which has the drawback of requiring too many man-hours for mass production.
したがって、本発明の目的はエージング時間を短縮し得
る、Zrを主成分とする電子放射性物質を使用したグロ
ースタータを提供することにある。Therefore, an object of the present invention is to provide a glow starter using an electron-emitting material containing Zr as a main component, which can shorten the aging time.
上記目的を達成するため本発明においては、ジルコニウ
ムとセシウムとを少なくとも含む電子放射性物質を電極
に被着してグロースタータを構成したことを特徴として
いる。In order to achieve the above object, the present invention is characterized in that a glow starter is constructed by depositing an electron-emitting substance containing at least zirconium and cesium on an electrode.
特に、本発明における最良の実施例様では少なくとも金
属粉末ジルコニウムに炭酸セシウムを添加して電極に被
着後、活性化してなる電子放射性物質を用いてグロース
タータを構成している。Particularly, in the best embodiment of the present invention, the glow starter is constructed using an electron-emitting substance obtained by adding cesium carbonate to at least metal powder zirconium, depositing it on the electrode, and then activating it.
かかる本発明の特徴的な構成によってエージング時間を
従来の約1時間から5〜10分八と大へに短縮すること
ができるようになり、その結果、量産性を大きく向上で
きるようになった。Due to the characteristic configuration of the present invention, the aging time can be greatly shortened from the conventional one hour to 5 to 10 minutes, and as a result, mass productivity can be greatly improved.
〔発明の実施例〕 以下、本発明を図を用いて詳細に述べる。[Embodiments of the invention] Hereinafter, the present invention will be described in detail using figures.
はじめに、本発明の原理について簡単に述べる。First, the principle of the present invention will be briefly described.
例えば、Vs108V以下、Vend 75 V以上の
特性を必要とするグロースタータで、電子放射性物質と
してZrを主成分とするものを用いた場合には排気中の
活性化不足をエージング時間で補なうが、V s 、
Vend特性が最も低下するまでには約1時間のエージ
ング時間を要することは前述した通りである。For example, in a glow starter that requires characteristics of Vs 108 V or less and Vend 75 V or more, if a material containing Zr as the main component is used as the electron radioactive material, the aging time will compensate for the lack of activation in the exhaust gas. , V s ,
As described above, it takes approximately 1 hour of aging time for the Vend characteristics to deteriorate the most.
そこで、本発明ではこのエージング時間を短縮するため
に、Zrよりも活性化が容易で、かつ仕事関数の低い電
子放射性物質、すなわちCsを添加したものであり、そ
の結果、短時間で初期特性を確保し、実用働程中にZr
を活性化促進させて安定した働程特性を得るようにした
ものである。Therefore, in the present invention, in order to shorten this aging time, an electron-emitting substance that is easier to activate than Zr and has a lower work function, that is, Cs, is added.As a result, the initial characteristics can be restored in a short time. Ensure Zr during the actual working process.
The activation is accelerated to obtain stable working characteristics.
次に、本発明の一実施例を第1図により説明する。バル
ブ1と封着したステム2には固定電極3とインナーリー
ド4とが植設されており、このインナーリード4にはバ
イメタルよりなる可動電極5が接続されている。可動電
極5は固定電極3と小間隙をおいて対向して設けられて
おり、グロー放電による熱で短絡回路を形成する。両電
極3゜5には接点部を除いて電子放射性物質6としてZ
rメタル粉末とZrに対してCs CO3を0.03〜
1.5%の重量比で添加したものを用い、これをNCバ
インダーで塗料として被着させる。Next, one embodiment of the present invention will be described with reference to FIG. A fixed electrode 3 and an inner lead 4 are implanted in a stem 2 that is sealed with the bulb 1, and a movable electrode 5 made of bimetal is connected to the inner lead 4. The movable electrode 5 is provided facing the fixed electrode 3 with a small gap therebetween, and forms a short circuit by heat generated by glow discharge. Z as an electron radioactive material 6 is placed on both electrodes 3°5 except for the contact portions.
r Cs CO3 for metal powder and Zr from 0.03 to
This was added at a weight ratio of 1.5%, and this was applied as a paint using an NC binder.
この時、電子放射性物質6の被着量はZrを0.05〜
ll11gの範囲とすることが特性的に最も実用に適し
ている。封入ガス7はN e 十A r 3〜12%の
混合ガスを40〜100Torr封入するのが実用的で
ある。At this time, the deposited amount of the electron radioactive substance 6 is Zr 0.05~
A range of 111g is most suitable for practical use in terms of characteristics. It is practical to fill the gas 7 with a mixed gas of 3 to 12% Ne and Ar at 40 to 100 Torr.
代表的な実施例によれば、Zrに対し重量比で0.4%
のCs C03を添加した電子放射性物質を、Zrの重
量が0.1〜0.2mgになるように電極に被着し、封
入ガスはN a + A r 8%混合ガスを約5QT
orr封入してグロースタータをつくり約10分間エー
ジング後のV s 、 Vend特性を点滅試験により
測定した結果を第2図に示す。同時に、比較のためにつ
くったZrのみを電子放射性物質に用い、封入ガスにN
e + A r 0 、2%混合ガスを約100To
rr封入したグロースタータの試験結果と対比すると、
Zrのみでは30分のエージングで初特性としてはV
s 、 Vendとも設定値を得られるが、働程中にV
s、Vendが低下してVend特性は設定値以下とな
る。この結果から、対策の手段は封入ガスの混合比を変
えてVsを高くし、かつ、エージング時間を長くしてV
s r Vendを安定領域まで下げることは考えら
れるが、さらに、エージング時間を長くすることは量産
的でない。According to a typical example, 0.4% by weight of Zr
An electron radioactive substance doped with Cs C03 was deposited on the electrode so that the weight of Zr was 0.1 to 0.2 mg, and the filled gas was a mixture of Na + Ar 8% at a rate of about 5QT.
FIG. 2 shows the results of measuring the V s and Vend characteristics by a flashing test after aging for about 10 minutes. At the same time, only Zr produced for comparison was used as the electron radioactive material, and N was added to the filler gas.
e + A r 0, 2% mixed gas about 100 To
Comparing with the test results of the glow starter enclosed in rr,
With only Zr, the initial characteristics are V after 30 minutes of aging.
The set values can be obtained for both s and Vend, but during the working process, V
s and Vend decrease, and the Vend characteristic becomes less than the set value. Based on this result, the countermeasures are to increase the Vs by changing the mixture ratio of the filler gas, and to increase the aging time to increase the Vs.
Although it is conceivable to lower s r Vend to a stable region, further increasing the aging time is not suitable for mass production.
これに対して本実施例のZ r 十Cs CO30,4
%添加したグロースタータは約10分間のエージングで
V s 、 Vend特性は安定領域にあり、設定値を
十分に満足出来るものである。On the other hand, in this example, Z r + Cs CO30,4
After aging for about 10 minutes, the V s and Vend characteristics of the glow starter with the addition of 10% are in the stable range, and the set values can be fully satisfied.
CsC○3の添加量はCsの仕事関数がZrより低いた
め微量におさえなければVendが下り過ぎるし、反対
に少な過ぎるとエージング時間短縮の効果不足となるた
めZrに対し重量比で0.03〜1.5%の添加が実用
的に好ましい。また、Zrの被着量は少ないと短寿命と
なり、多過ぎると活性化エージング不足をきたし、また
はCs量との兼合いでVend低下となるので0.05
〜1mgとするのが好ましい。すなわち、Zrに対する
Cs量は被着量と添加比との両方で規制することが最良
であり、その結果として活性化エージング時間の短縮の
効果が得られる。Since the work function of Cs is lower than that of Zr, the amount of CsC○3 added must be kept to a very small amount, otherwise the Vend will drop too much.On the other hand, if it is too small, the effect of shortening the aging time will be insufficient, so the weight ratio of Cs to Zr is 0.03. Addition of ~1.5% is practically preferred. In addition, if the amount of Zr deposited is small, the life will be shortened, and if it is too much, activation aging will be insufficient, or the Vend will decrease due to the balance with the amount of Cs, so 0.05
It is preferable to set it as 1 mg. That is, it is best to control the amount of Cs relative to Zr by both the amount of deposit and the addition ratio, and as a result, the effect of shortening the activation aging time can be obtained.
なお、電子放射性物質でZrより仕事関係の低い材料と
しては、Cs以外にBa、]Ra、Ce等が知られてい
るが、Zrメタル粉末をNCバイダーで懸たく液として
電極に被着させる場合には、夫々使いにくい欠点があり
、Csを用いることが最も適している。In addition to Cs, Ba, ]Ra, Ce, etc. are known as electron-radioactive materials with lower work-related properties than Zr. However, when Zr metal powder is applied as a liquid to an electrode using an NC binder, Each of these has drawbacks that make them difficult to use, and it is most suitable to use Cs.
なお、上述の実施例では電子放射性物質としてZrとC
sとを含む物質について述べたが、他の電子放射性物質
がさらに含まれていても良いことは言うまでもない。In addition, in the above-mentioned example, Zr and C were used as the electron radioactive substances.
Although the substance containing s has been described, it goes without saying that other electron radioactive substances may also be included.
〜120■で険相する蛍光ランプ用のグロースタータテ
、B電圧80v以上、Vend75V以上の設定値に対
して前述の通りの満足出来る特性を得られると同時に、
エージング時間をZrのみの場合に対し大幅に短縮でき
るために生産性の大幅な向上が可能となった。At the same time, it is possible to obtain satisfactory characteristics as described above for the vertical glow starter for fluorescent lamps, B voltage 80 V or more, and Vend 75 V or more, which are unstable at ~120 ■.
Since the aging time can be significantly shortened compared to the case of using only Zr, it has become possible to significantly improve productivity.
第1図は本発明によるグロースタータの一部断面図、第
2図はZrのみを電子放射性物質としたよる働程特性比
較図である。
1・・バルブ、2・・・ステム、3・・・固定電極、4
・・・インナーリード、5・・・バイメタル、6・・・
電子放射性物質、7・・・封入ガス。FIG. 1 is a partial sectional view of a glow starter according to the present invention, and FIG. 2 is a comparison diagram of working characteristics using only Zr as an electron emitting substance. 1... Valve, 2... Stem, 3... Fixed electrode, 4
...Inner lead, 5...Bimetal, 6...
Electron radioactive material, 7...Enclosed gas.
Claims (1)
射性物質が被着された電極を備えてなることを特徴とす
るグロースタータ。 2、上記電子放射性物質が少なくとも金属粉末ジルコニ
ウムに炭酸セシウムを添加して電極に被着後、活性化さ
れたものであることを特徴とする第1項のグロースター
タ。 3、上記ジルコニウムの被着量が0.05〜1mgであ
り、かつ、上記炭酸セシウムが上記ジルコニウムに対し
て重量比で0.03〜1.5%添加されていることを特
徴とする第2項のグロースタータ。[Claims] 1. A glow starter comprising an electrode coated with an electron-emitting substance containing at least zirconium and cesium. 2. The glow starter according to item 1, wherein the electron emissive substance is activated by adding cesium carbonate to at least metal powder zirconium and depositing it on the electrode. 3. A second method characterized in that the amount of the zirconium deposited is 0.05 to 1 mg, and the cesium carbonate is added in a weight ratio of 0.03 to 1.5% to the zirconium. Glow starter of term.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2503384A JPS60170151A (en) | 1984-02-15 | 1984-02-15 | Glow starter |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2503384A JPS60170151A (en) | 1984-02-15 | 1984-02-15 | Glow starter |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60170151A true JPS60170151A (en) | 1985-09-03 |
Family
ID=12154593
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2503384A Pending JPS60170151A (en) | 1984-02-15 | 1984-02-15 | Glow starter |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60170151A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5335969A (en) * | 1991-06-26 | 1994-08-09 | Okamura Corporation | Chair |
WO2004030419A1 (en) * | 2002-09-30 | 2004-04-08 | Huo Nang Development Co. Ltd. | A starter for fluorescent lamp and a fluorescent lamp using the starter |
KR100464284B1 (en) * | 2001-05-29 | 2005-01-03 | 도시바 라이텍쿠 가부시키가이샤 | Glow discharge lamp , electrode thereof and luminaire |
WO2006046598A1 (en) * | 2004-10-27 | 2006-05-04 | Matsushita Electric Industrial Co., Ltd. | Glow starter and method for manufacturing same |
-
1984
- 1984-02-15 JP JP2503384A patent/JPS60170151A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5335969A (en) * | 1991-06-26 | 1994-08-09 | Okamura Corporation | Chair |
KR100464284B1 (en) * | 2001-05-29 | 2005-01-03 | 도시바 라이텍쿠 가부시키가이샤 | Glow discharge lamp , electrode thereof and luminaire |
WO2004030419A1 (en) * | 2002-09-30 | 2004-04-08 | Huo Nang Development Co. Ltd. | A starter for fluorescent lamp and a fluorescent lamp using the starter |
AU2002349494B2 (en) * | 2002-09-30 | 2008-08-07 | Huo Nang Development Co. Ltd. | A starter for fluorescent lamp and a fluorescent lamp using the starter |
JP2009283466A (en) * | 2002-09-30 | 2009-12-03 | Huo Nang Development Co Ltd | Glow starter for fluorescent lamp and compact fluorescent lamp, and fluorescent lamp fixture related thereto |
WO2006046598A1 (en) * | 2004-10-27 | 2006-05-04 | Matsushita Electric Industrial Co., Ltd. | Glow starter and method for manufacturing same |
JP2006127865A (en) * | 2004-10-27 | 2006-05-18 | Matsushita Electric Ind Co Ltd | Glow starter and its manufacturing method |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4105910A (en) | Fluorescent lamp with an integral fail-safe and auxiliary-amalgam component | |
US4145634A (en) | Fluorescent lamp having integral mercury-vapor pressure control means | |
US3798492A (en) | Emissive electrode | |
US4319158A (en) | Electrode for discharge lamp | |
US5412289A (en) | Using a magnetic field to locate an amalgam in an electrodeless fluorescent lamp | |
GB2051649A (en) | Arc tubes for high-pressure sodium discharge lamps | |
US2724070A (en) | Cathode coating for electrical discharge devices and method for making the same | |
JPS60170151A (en) | Glow starter | |
US6503117B2 (en) | Methods for making electrode assemblies for fluorescent lamps | |
CA1194074A (en) | High intensity vapour discharge lamp | |
US3837909A (en) | Coated coil emissive electrode | |
JP3363816B2 (en) | Discharge tube electrode and discharge tube using the same | |
JPH0628967A (en) | Dispenser cathode | |
CA1276965C (en) | Hot cathode in wire form coated with rare and alkaline earth metal oxides containing barium oxide | |
US20030057814A1 (en) | Fluorescent lamp with reduced sputtering | |
US6091189A (en) | Cathode for an electron tube | |
US2769708A (en) | Thermionic cathode and method of making the same | |
US3951874A (en) | Method for preparing electron emissive coatings | |
JP2001155679A (en) | Gas discharge lamp | |
JPS58216353A (en) | Starter lamp | |
US4837483A (en) | Glow discharge starter containing boron | |
JPH06223776A (en) | Electrode for fluorescent lamp | |
CA1172683A (en) | Electron emitting coating in metal halide arc lamp | |
JPS59121750A (en) | Cold-cathode discharge lamp | |
JPH09190761A (en) | Cathode for electron tube |