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JPH0340463B2 - - Google Patents
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JPH0340463B2 - - Google Patents

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Publication number
JPH0340463B2
JPH0340463B2 JP57211322A JP21132282A JPH0340463B2 JP H0340463 B2 JPH0340463 B2 JP H0340463B2 JP 57211322 A JP57211322 A JP 57211322A JP 21132282 A JP21132282 A JP 21132282A JP H0340463 B2 JPH0340463 B2 JP H0340463B2
Authority
JP
Japan
Prior art keywords
arc tube
metal
ceramic body
luminescent
metal halide
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.)
Expired - Lifetime
Application number
JP57211322A
Other languages
Japanese (ja)
Other versions
JPS59101755A (en
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 filed Critical
Priority to JP21132282A priority Critical patent/JPS59101755A/en
Publication of JPS59101755A publication Critical patent/JPS59101755A/en
Publication of JPH0340463B2 publication Critical patent/JPH0340463B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00Gas-discharge or vapour-discharge lamps
    • H01J61/02Details
    • H01J61/12Selection of substances for gas fillings; Specified operating pressure or temperature

Landscapes

  • Discharge Lamp (AREA)
  • Discharge Lamps And Accessories Thereof (AREA)

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は発光管内に始動特性を改善するために
放射性物質を封入したメタルハライドランプに関
する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a metal halide lamp in which a radioactive substance is sealed in the arc tube to improve starting characteristics.

〔発明の技術的背景およびその問題点〕[Technical background of the invention and its problems]

従来からメタルハライドランプにおいて、その
始動を容易にするためにエミツターとしてトリウ
ム(Th)や酸化トリウム(ThO2)を使用するこ
とが知られている。また、これ等トリウムが発光
管内に封入した金属ハロゲン化物のハロゲンと反
応してハロゲン化トリウムとなり、これが発光し
て他の効率の高い封入物の発光を抑制して光束低
下の原因となつたり、ランプ電圧の上昇を招く等
の欠点に対処して、トリウムに代えてハロゲンな
どと反応しない半減期の短かいエミツター(放射
性物質)を使用した提案(特開昭56−126248号公
報)もある。さらに、前記半減期の短かい放射性
物質を安全性の面から取扱いやすくするため、放
射性物質をセラミツク体に分散させたものも提案
(特開56−126248号公報)されている。しかしな
がら、放射性物質を分散させるセラミツク体は、
通常ナトリウム酸化物、カルシウム酸化物等のア
ルカリ金属やアルカリ土類金属等の放電灯にとつ
て有害な成分を含んでおり、セラミツク体を発光
管内に封入した場合、長時間の点灯によつて、前
記アルカリ金属やアルカリ土類金属が発光金属た
とえばスカンジウムSc、デイスプロシウムDy等
の希土類金属のハロゲン化物と置換反応をおこ
し、その酸化物が安定なSc,Dy等の発光金属は、
ナトリウム酸化物Na2O、カルシウム酸化物CaO
等のNa,Caと置換して安定な酸化物Sc2O3
Dy2O3等を生成して、その有効量が減少し、発光
効率を低下させるなどの欠点を生じた。
It has been known to use thorium (Th) or thorium oxide (ThO 2 ) as an emitter in metal halide lamps in order to facilitate their starting. In addition, these thorium reacts with the halogen of the metal halide sealed in the arc tube to form thorium halide, which emits light and suppresses the light emission of other highly efficient fillers, causing a decrease in luminous flux. In order to address the drawbacks such as an increase in lamp voltage, there is also a proposal (Japanese Patent Application Laid-Open No. 126248/1983) to use an emitter (radioactive substance) with a short half-life that does not react with halogen etc. in place of thorium. Furthermore, in order to make it easier to handle radioactive substances with short half-lives from the viewpoint of safety, a ceramic body in which radioactive substances are dispersed has been proposed (Japanese Patent Laid-Open No. 56-126248). However, the ceramic body that disperses radioactive materials is
Normally, discharge lamps contain components such as alkali metals and alkaline earth metals such as sodium oxide and calcium oxide that are harmful to discharge lamps, and when a ceramic body is enclosed in an arc tube, it may cause damage due to long-term lighting. The alkali metals and alkaline earth metals undergo a substitution reaction with halides of rare earth metals such as scandium Sc and disprosium Dy, and the luminescent metals such as Sc and Dy, whose oxides are stable, are
Sodium oxide Na2O , calcium oxide CaO
Sc 2 O 3 , which is a stable oxide that can be substituted with Na and Ca, such as Sc 2 O 3 ,
This resulted in disadvantages such as generation of Dy 2 O 3 and the like, resulting in a decrease in its effective amount and a decrease in luminous efficiency.

〔発明の目的〕[Purpose of the invention]

本発明は前記欠点に対処してなされたもので、
発光管内に放射性物質分散セラミツク体を封入し
て、始動が容易で、しかも発光効率の低下が少な
いメタルハライドランプを提供することを目的と
する。
The present invention has been made to address the above-mentioned drawbacks.
An object of the present invention is to provide a metal halide lamp which is easy to start and has little reduction in luminous efficiency by enclosing a radioactive substance-dispersed ceramic body in an arc tube.

〔発明の概要〕[Summary of the invention]

本発明は発光管内に始動用希ガス、水銀および
発光金属とともに放射性物質を分散担持させたセ
ラミツク体はそれ自体に含まれる不純物が前記発
光金属で置換されたものであることを特徴とす
る。
The present invention is characterized in that the ceramic body in which a radioactive substance is dispersed and supported in the arc tube along with a starting rare gas, mercury, and a luminescent metal has impurities contained therein replaced with the luminescent metal.

〔発明の実施例〕[Embodiments of the invention]

以下、本発明の詳細を実施例を参照する。 Hereinafter, details of the present invention will be described with reference to Examples.

天然に産出するゼオライトを径1〜3mm程度の
顆粒状にて焼成すると、一般式M2oO・
Al2O3・xSiO2・yH2O (但しMは金属カチオン、nは原子価、xとy
は係数) 例えばNa12(AlO212(SiO212〕・27H2Oなるセ
ラミツクが得られる。
When naturally occurring zeolite is fired into granules with a diameter of about 1 to 3 mm, it has the general formula M 2 / o O.
Al 2 O 3・xSiO 2・yH 2 O (where M is a metal cation, n is a valence, x and y
For example, a ceramic such as Na 12 (AlO 2 ) 12 (SiO 2 ) 12 ]·27H 2 O is obtained.

次にこの物を塩化アンモニウムNH4Cl溶液中
で洗条するとNaイオンがNH4イオンと置換され
て、 (NH412〔(AlO212(SiO212〕・27H2Oとなる。
Next, when this material is washed in an ammonium chloride NH 4 Cl solution, Na ions are replaced with NH 4 ions, resulting in (NH 4 ) 12 [(AlO 2 ) 12 (SiO 2 ) 12 ]・27H 2 O. .

この物を約800℃で仮焼成するとNH3が飛散し
て H12〔(AlO212(SiO212〕・27H2O なるH型ゼオライトが形成される。しかしなが
ら、この物にはなお若干のNaイオンが残留する
ので、さらに発光管内に封入する発光金属のハロ
ゲン化物たとえば沃化スカンジウムScI3の蒸気中
にひたす。
When this material is calcined at about 800° C., NH 3 is scattered and H-type zeolite H 12 [(AlO 2 ) 12 (SiO 2 ) 12 ]·27H 2 O is formed. However, since some Na ions still remain in this product, it is further immersed in the vapor of a luminescent metal halide, such as scandium iodide ScI 3 , which is sealed in the arc tube.

すなわち、前記H型ゼオライトをたとえば石英
容器中に入れ、真空引きしたのちScI3を封入し、
1000℃前後で数時間加熱すれば残留するNaイオ
ンは発光管特性に悪い影響を与えない程度にまで
充分にScイオンで置換することができる。
That is, the H-type zeolite is placed in, for example, a quartz container, evacuated, and then ScI 3 is sealed,
By heating at around 1000°C for several hours, the remaining Na ions can be sufficiently replaced with Sc ions to the extent that they do not adversely affect the characteristics of the arc tube.

このようにして、発光管に対し有害な成分を発
光金属で置換したゼオライトは次にたとえば放射
性物質の一種147pmの塩酸溶液に浸漬すれば、ゼ
オライトに含まれる水素イオンと147pmイオンと
が置換するか、もしくは147pm原子がゼオライト
の粒子間に浸入し捕捉される。このように放射性
物質を含浸させたゼオライトは次に再び800℃前
後で20分程度焼成して塩素イオンを飛散離脱させ
放射性物質分散ゼオライト体が得られる。
In this way, the zeolite whose components harmful to the arc tube have been replaced with luminescent metals is then immersed in, for example, a 147 pm hydrochloric acid solution, which is a type of radioactive substance, and the hydrogen ions contained in the zeolite are replaced with 147 pm ions. Alternatively, the 147 pm atoms can penetrate between the zeolite particles and become trapped. The zeolite impregnated with the radioactive substance in this way is then fired again at around 800°C for about 20 minutes to scatter off the chlorine ions and obtain a radioactive substance-dispersed zeolite body.

この物はさらに必要に応じたとえばアルミナ、
シリカ等を主成分とする水溶性ペーストに浸漬、
乾燥したのち1000℃前後で焼成して、放射性物質
を含まない表面層を形成して取扱い上のより一層
の安全性を計ることもできる。
This material can be further treated with alumina, for example, as required.
Immersed in a water-soluble paste mainly composed of silica, etc.
After drying, it can be fired at around 1,000°C to form a surface layer that does not contain radioactive substances, making it even safer to handle.

このように形成された放射性物質147pm含浸ゼ
オライトを147pmが5×10-6mg(放射能量として
5マイクロキユリー)となる量を水銀50mg、アル
ゴンガス25トール、発光金属スカンジウムおよび
ナトリウムの各沃化物計30mgと共に内径20mm、主
電極間距離42mmの石英製発光管内に封入し、この
発光管を内部を真空又は不活性ガスを充填した外
管内に封装して400Wのメタルハライドランプを
作る。
The zeolite impregnated with the radioactive substance 147 pm thus formed was mixed with 50 mg of mercury, 25 torr of argon gas, and each of the luminescent metals scandium and sodium in an amount such that 147 pm was 5 × 10 -6 mg (5 microcuries as the amount of radioactivity). A total of 30 mg of iodide is sealed in a quartz arc tube with an inner diameter of 20 mm and a distance between main electrodes of 42 mm, and this arc tube is sealed inside an outer tube filled with vacuum or inert gas to make a 400 W metal halide lamp.

このメタルハライドランプはたとえば概略第1
図に示すように点灯回路によつて使用される。す
なわち、点線で示す放電灯外管1内に抵抗6、バ
イメタルスイツチ7およびグロー点灯管8からな
る直列回路が発光管2と並列に接続され、点灯管
8とバイメタルスイツチ7の中間点から抵抗9を
介して起動補助電極5に接続されている。発光管
2は一対の主電極4a,4bを有し、これ等電極
は終局的に安定器10を介して電源11に接続さ
れている。このような点灯回路において、ランプ
に電圧が印加されると、まず抵抗6、バイメタル
スツチ7、グロー点灯管8を介して電流が流れ、
グロー点灯管8が動作し回路を断続する。この断
続電流により安定器10からキツク電圧が発生す
る。
This metal halide lamp, for example,
It is used by the lighting circuit as shown in the figure. That is, a series circuit consisting of a resistor 6, a bimetallic switch 7, and a glow lighting tube 8 is connected in parallel with the luminous tube 2 in the discharge lamp outer bulb 1 shown by a dotted line, and from the midpoint between the lighting tube 8 and the bimetallic switch 7, It is connected to the starting auxiliary electrode 5 via a resistor 9. The arc tube 2 has a pair of main electrodes 4a, 4b, which are ultimately connected to a power source 11 via a ballast 10. In such a lighting circuit, when a voltage is applied to the lamp, a current first flows through the resistor 6, the bimetallic switch 7, and the glow lighting tube 8.
The glow lighting tube 8 operates to interrupt the circuit. This intermittent current generates a kick voltage from the ballast 10.

一方、発光管2内に封入された放射性物質分散
セラミツク体3から強いエネルギーを有した荷電
粒子が発生し、始動用希ガスを電離する。
On the other hand, charged particles with strong energy are generated from the radioactive substance-dispersed ceramic body 3 sealed in the arc tube 2 and ionize the starting rare gas.

これによつて、起動補助電極5と一方の主電極
4a間にパルス印加時に微少電流が流れ、成長し
て発光管が起動し点灯するに到る。
As a result, a minute current flows between the starting auxiliary electrode 5 and one of the main electrodes 4a when a pulse is applied, and grows to start the arc tube and light it up.

このときの始動時間はほとんど瞬時に近いきわ
めて短時間しか要さなかつた。
The starting time at this time was almost instantaneous and required only a very short time.

また、特に発光効率の低下率は点灯5000時間後
においても20%程度で、従来の放射性物質を分散
担持させるセラミツク体つまりゼオライトに含ま
れる不純物ナトリウムを発光金属で置換しなかつ
たランプの同じ点灯時間後の発光効率の低下50%
よりもはるかに優れていた。
In particular, the rate of decrease in luminous efficiency is about 20% even after 5000 hours of lighting, which is the same lighting time as a conventional lamp in which the impurity sodium contained in zeolite, which is a ceramic body that disperses radioactive substances, is not replaced with luminescent metal. Luminous efficiency decreases after 50%
It was much better than that.

なお、前記実施例ではセラミツク体としてゼオ
ライトの例について述べたが、本発明はもちろん
これに限定されるものではなく主成分が
3Al2O3・2SiO2であるムライト、主成分がAl4
(OH)8・Si4O10であるカオリナイト、主成分が
Al4(OH)8・Si4O10・nH2Oであるハロイサイト等
その主成分がメタルハライドランプの発光管内に
封入された際に無害であるものならば同様に適用
できるものである。また、本発明でセラミツク体
自体に含まれる不純物とは、セラミツク体が発光
管内に封入使用された場合に、発光金属と置換し
てより安定な発光金属の酸化物の生成をゆるし、
それによつて発光管内の有効な発光金属量を減少
して発光効率を低下させるような物を指し、した
がつて発光金属の種類によつて不純物の範囲は異
なるが、一般的にはアルカリ金属およびアルカリ
土類金属の場合が多い。一方、発光金属としては
Scを含む希土類金属、Al,Sn等の場合が特には
適し、発光管内に封入する形態としてはハロゲン
化物の形が望ましい。
Although zeolite was used as the ceramic body in the above embodiment, the present invention is not limited to this, and the main component may be zeolite.
Mullite, which is 3Al 2 O 3 2SiO 2 , the main component is Al 4
Kaolinite, whose main component is (OH) 8・Si 4 O 10
Halloysite, which is Al 4 (OH) 8 · Si 4 O 10 · nH 2 O, etc., can be similarly applied if its main component is harmless when it is enclosed in the arc tube of a metal halide lamp. In addition, in the present invention, impurities contained in the ceramic body itself refer to impurities that, when the ceramic body is sealed and used in an arc tube, replace luminescent metals and allow the formation of more stable oxides of luminescent metals.
This refers to substances that reduce the effective amount of luminescent metal in the arc tube and reduce luminous efficiency.The range of impurities differs depending on the type of luminescent metal, but in general, alkali metals and Often alkaline earth metals. On the other hand, as a luminescent metal
Rare earth metals including Sc, Al, Sn, etc. are particularly suitable, and halides are preferable for sealing in the arc tube.

さらに、放射性物質も前記147pmに限られるも
のではなく、14C,22NA,60Co,55Fe,45Ca,60Ni,
65Zn,54Mn,90Sr,106Ru,110Ag、125Sb,134Cs,137C
s,
133Ba,144Ce,154Eu,155Eu,195Au,240Tl,227Ac,
241Am,242Cm,244Cm,252Cf,210Pb,226Ra,228Ra,
228Thなどのその半減期が0.5年〜10年のものが望
ましい。
Furthermore, the radioactive substances are not limited to the above 147 pm, but include 14 C, 22 NA, 60 Co, 55 Fe, 45 Ca, 60 Ni,
65 Zn, 54 Mn, 90 Sr, 106 Ru, 110 Ag, 125 Sb, 134 Cs, 137 C
s,
133 Ba, 144 Ce, 154 Eu, 155 Eu, 195 Au, 240 Tl, 227 Ac,
241 Am, 242 Cm, 244 Cm, 252 Cf, 210 Pb, 226 Ra, 228 Ra,
Those with a half-life of 0.5 to 10 years, such as 228 Th, are preferable.

何故ならば、半減期が0.5年未満であると、減
衰が急速であるためランプの寿命中経減衰が完了
してしまつて始動性能が寿命途中で著しく低下す
ることになる。
This is because if the half-life is less than 0.5 years, the decay will be rapid and the lamp will complete its decay over the course of its life, resulting in a significant drop in starting performance.

一方、半減期が10年を越すように長すぎると、
放射線の減衰が遅々として進まず、安全面で有害
となり得るからである。
On the other hand, if the half-life is too long, exceeding 10 years,
This is because the attenuation of radiation progresses slowly, which can be harmful in terms of safety.

〔発明の効果〕〔Effect of the invention〕

以上詳述したように、本発明のメタルハライド
ランプは放射性物質を分散担持させるセラミツク
体を、それ自体に含まれる不純物を発光金属で置
換するようにしたので、始動を容易にし、かつ、
発光効率の低下をも少なくすることができる。
As detailed above, in the metal halide lamp of the present invention, the impurities contained in the ceramic body dispersively supporting the radioactive substance are replaced with a luminescent metal, so that it is easy to start, and
Decrease in luminous efficiency can also be reduced.

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

図は本発明の一実施例であるメタルハライドラ
ンプの点灯回路を示す。 1……外管、2……発光管、3……放射性物質
分散セラミツク体、4a,4b……主電極、5…
…起動補助電極、6……抵抗、7……バイメタル
スイツチ、8……グロー点灯管、9……抵抗、1
0……安定器。
The figure shows a lighting circuit for a metal halide lamp, which is an embodiment of the present invention. DESCRIPTION OF SYMBOLS 1... Outer tube, 2... Arc tube, 3... Radioactive substance dispersed ceramic body, 4a, 4b... Main electrode, 5...
... Starting auxiliary electrode, 6 ... Resistor, 7 ... Bimetal switch, 8 ... Glow lighting tube, 9 ... Resistor, 1
0... Stabilizer.

Claims (1)

【特許請求の範囲】 1 発光管内に始動用希ガス、水銀および発光金
属とともに放射性物質分散セラミツク体を封入し
たメタルハライドランプにおいて、前記セラミツ
ク体はその成分の一部が前記発光金属で置換され
たものであることを特徴とするメタルハライドラ
ンプ。 2 前記発光金属は希土類金属、アルミニウムお
よび錫の少なくとも1種を含むものであることを
特徴とする特許請求の範囲第1項記載のメタルハ
ライドランプ。
[Scope of Claims] 1. A metal halide lamp in which a radioactive substance-dispersed ceramic body is enclosed in an arc tube together with a starting rare gas, mercury, and a luminescent metal, wherein a part of the components of the ceramic body are replaced with the luminescent metal. A metal halide lamp characterized by: 2. The metal halide lamp according to claim 1, wherein the luminescent metal contains at least one of a rare earth metal, aluminum, and tin.
JP21132282A 1982-12-03 1982-12-03 Metal halide lamp Granted JPS59101755A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21132282A JPS59101755A (en) 1982-12-03 1982-12-03 Metal halide lamp

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21132282A JPS59101755A (en) 1982-12-03 1982-12-03 Metal halide lamp

Publications (2)

Publication Number Publication Date
JPS59101755A JPS59101755A (en) 1984-06-12
JPH0340463B2 true JPH0340463B2 (en) 1991-06-19

Family

ID=16604027

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21132282A Granted JPS59101755A (en) 1982-12-03 1982-12-03 Metal halide lamp

Country Status (1)

Country Link
JP (1) JPS59101755A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61216232A (en) * 1985-03-20 1986-09-25 Matsushita Electronics Corp Metal halide lamp
US5698943A (en) * 1996-03-22 1997-12-16 Osram Sylvania Inc. Starting flag for use in mercury discharge lamp and lamp employing same

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6034221B2 (en) * 1980-06-18 1985-08-07 株式会社東芝 metal vapor discharge lamp
JPS5753064A (en) * 1980-09-16 1982-03-29 Toshiba Corp Metal halide lamp

Also Published As

Publication number Publication date
JPS59101755A (en) 1984-06-12

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