JPH0536381A - Rapid start type fluorescent lamp - Google Patents

Rapid start type fluorescent lamp

Info

Publication number
JPH0536381A
JPH0536381A JP3191466A JP19146691A JPH0536381A JP H0536381 A JPH0536381 A JP H0536381A JP 3191466 A JP3191466 A JP 3191466A JP 19146691 A JP19146691 A JP 19146691A JP H0536381 A JPH0536381 A JP H0536381A
Authority
JP
Japan
Prior art keywords
phosphor
film
fluorescent lamp
mercury
type fluorescent
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
Application number
JP3191466A
Other languages
Japanese (ja)
Other versions
JP3343362B2 (en
Inventor
Hidenori Ito
秀徳 伊藤
Yoji Yuge
洋二 弓削
Kimiyoshi Nagasawa
公義 長澤
Masaaki Tamaya
正昭 玉谷
Kenji Terajima
賢二 寺島
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
Toshiba Lighting and Technology Corp
Original Assignee
Toshiba Corp
Toshiba Lighting and Technology 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, Toshiba Lighting and Technology Corp filed Critical Toshiba Corp
Priority to JP19146691A priority Critical patent/JP3343362B2/en
Publication of JPH0536381A publication Critical patent/JPH0536381A/en
Application granted granted Critical
Publication of JP3343362B2 publication Critical patent/JP3343362B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

(57)【要約】 【目的】けい光体層の黄変やEC膜の黒化を防止したラ
ピッドスタート形けい光ランプを提供する。 【構成】バルブ1の内面に透明性導電膜5およびけい光
体層6を形成し、このバルブ内に水銀および希ガスを封
入したラピッドスタ−ト形けい光ランプにおいて、けい
光体層を構成するけい光体は、粒子径74〜44μmの
還元鉄粉との接触時にけい光体1g当り−0.5〜+
1.5マイクロク−ロンの電荷を帯電したことを特徴と
する。 【作用】けい光体の帯電傾向を制御したので、けい光体
と水銀および水銀化合物の吸着性を規制することがで
き、けい光体の黄変やEC膜の黒化を防止する。
(57) [Abstract] [Purpose] To provide a rapid start type fluorescent lamp in which yellowing of a phosphor layer and blackening of an EC film are prevented. [Structure] A transparent conductive film 5 and a phosphor layer 6 are formed on the inner surface of a bulb 1, and a phosphor layer is formed in a rapid start type fluorescent lamp in which mercury and a rare gas are enclosed. The fluorescent substance is -0.5 to + per 1 g of the fluorescent substance when contacted with reduced iron powder having a particle diameter of 74 to 44 μm.
It is characterized by being charged with an electric charge of 1.5 microcoulombs. Since the charging tendency of the phosphor is controlled, the adsorptivity of the phosphor and mercury and mercury compounds can be regulated, and yellowing of the phosphor and blackening of the EC film can be prevented.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、ラピッドスタート形け
い光ランプにおいて、けい光体層やEC膜の黒化防止手
段に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to means for preventing blackening of a phosphor layer or an EC film in a rapid start type fluorescent lamp.

【0002】[0002]

【従来の技術】ラピッドスタート形けい光ランプは、発
光管バルブの内面に、例えば酸化錫SnOなどからなる
透明性導電膜(EC膜=ネサ膜)を形成するとともに、
このEC膜の内面にけい光体被膜を形成してあり、EC
膜が管壁抵抗を引下げる役割を果たすので始動性に優れ
たけい光ランプとして知られている。
2. Description of the Related Art In a rapid start fluorescent lamp, a transparent conductive film (EC film = nesa film) made of, for example, tin oxide SnO is formed on the inner surface of an arc tube bulb.
A fluorescent substance film is formed on the inner surface of the EC film.
It is known as a fluorescent lamp which has an excellent starting property because the film plays a role of lowering the wall resistance.

【0003】そして、最近においては、高効率および高
演色性を得るため、狭い波長範囲で線状の発光スペクト
ルを有する赤、青、緑の3色のけい光体を組合わせた、
いわゆる3波長発光形けい光体を用いたラピッドスター
ト形けい光ランプが開発されている。
In recent years, in order to obtain high efficiency and high color rendering properties, a combination of three color phosphors of red, blue and green which have a linear emission spectrum in a narrow wavelength range,
Rapid start type fluorescent lamps using so-called three-wavelength light emitting type phosphors have been developed.

【0004】このようなラピッドスタート形けい光ラン
プは、バルブ内に水銀および1種または2種以上の希ガ
スを含む混合ガスが充填され、2つの電極を経て電極エ
ネルギ−を混合ガスに供給することによってこの混合ガ
ス中で陽光柱放電を生じるように構成されている。この
放電によって、主に紫外線が発生し、その大半は185
nmと254nmの波長を有しており、この紫外線はバルブ
内面に形成されている3波長発光形けい光体により、
赤、青、緑の3色の発光スペクトルに変換され、これら
3色の混合色の光が得られている。
In such a rapid start fluorescent lamp, a bulb is filled with a mixed gas containing mercury and one or more rare gases, and electrode energy is supplied to the mixed gas through two electrodes. As a result, a positive column discharge is generated in this mixed gas. This discharge mainly produces ultraviolet rays, most of which is 185
nm and 254 nm, and this ultraviolet ray is generated by the three-wavelength emission type phosphor formed on the inner surface of the bulb.
The red, blue, and green light emission spectra are converted to obtain mixed-color light of these three colors.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、このよ
うな3波長発光形けい光体を用いたラピッドスタート形
けい光ランプにおいては、長時間の使用にともなってけ
い光体被膜が黄変して光束が低下したり、またはEC膜
に暗褐色の帯状斑点による黒化現象が発生する場合があ
る。このような変色や黒化は、特に青色系けい光体およ
び緑色けい光体において著しい。
However, in a rapid start type fluorescent lamp using such a three-wavelength light emitting type fluorescent substance, the fluorescent substance coating turns yellow due to long-term use and the luminous flux is changed. Or the blackening phenomenon due to dark brown band-like spots may occur on the EC film. Such discoloration and blackening are remarkable especially in blue-based phosphors and green phosphors.

【0006】この原因について検討、究明したところ、
上記のけい光体はランプ点灯中に水銀および炭素や水素
などの不純物と反応した水銀化合物を吸着し易く、これ
ら吸着した水銀および水銀化合物はけい光体被膜の表面
からなかなか離れず、水銀はさらに不純物を取り込んで
水銀化合物を形成し、このような水銀化合物が黄色の変
色すること、およびこのような水銀化合物がEC膜の近
くまで到達してこれら水銀化合物とEC膜が電位差によ
り微放電を発生し、この放電により水銀化合物が黒く変
色してEC膜の黒化に至ると推察される。
[0006] When the cause of this is examined and investigated,
The above-mentioned phosphor easily adsorbs mercury and mercury compounds that have reacted with impurities such as carbon and hydrogen while the lamp is operating, and these adsorbed mercury and mercury compounds do not easily separate from the surface of the phosphor coating, and mercury is further absorbed. Impurity is taken in to form a mercury compound, and such a mercury compound turns yellow, and when such a mercury compound reaches near the EC film, the mercury compound and the EC film generate a slight discharge due to a potential difference. However, it is speculated that this discharge causes the mercury compound to turn black, resulting in blackening of the EC film.

【0007】このような黄変や黒化現象を防止する手段
として、EC膜の電気抵抗を高くすることにより電位差
を低くすることが考えられるが、このようにすると、管
壁抵抗が増大するので始動電圧が高くなり、始動が困難
になり、特に0℃以下の低温雰囲気で始動させようとす
ると、容易に始動しなくなり、このため、ランプの用途
が限られるなどの欠点を生じる。
As a means for preventing such a yellowing or blackening phenomenon, it is conceivable to lower the potential difference by increasing the electric resistance of the EC film. However, if this is done, the tube wall resistance increases. The starting voltage becomes high and the starting becomes difficult, and especially when trying to start in a low temperature atmosphere of 0 ° C. or less, the starting does not start easily, which causes drawbacks such as limited use of the lamp.

【0008】本発明はこのような事情にもとづきなされ
たもので、その目的とするところは、けい光体の黄変や
EC膜の黒化を防止することができるラピッドスタ−ト
形傾けい光ランプを提供しようとするものである。
The present invention has been made in view of the above circumstances, and an object thereof is to provide a rapid start type tilted light capable of preventing yellowing of a phosphor and blackening of an EC film. It is intended to provide a lamp.

【0009】[0009]

【課題を解決するための手段】本発明は、バルブの内面
に透明性導電膜およびけい光体層を形成し、このバルブ
内に水銀および希ガスを封入したラピッドスタ−ト形け
い光ランプにおいて、前記けい光体層を構成するけい光
体は、粒子径74〜44μmの還元鉄粉との接触時にけ
い光体1g当り−0.5〜+1.5マイクロク−ロンの
電荷を帯電したことを特徴とする。
DISCLOSURE OF THE INVENTION The present invention provides a rapid start type fluorescent lamp in which a transparent conductive film and a phosphor layer are formed on the inner surface of a bulb, and mercury and a rare gas are enclosed in the bulb. The phosphor constituting the phosphor layer is charged with a charge of −0.5 to +1.5 microcoulombs per 1 g of the phosphor when contacted with reduced iron powder having a particle size of 74 to 44 μm. Is characterized by.

【0010】[0010]

【作用】本発明者等は調査、実験および解析したとこ
ろ、ラピッドスタ−ト形けい光ランプにおいては、けい
光体の帯電傾向がけい光体の黄変やEC膜の黒化に密接
に関与していることを尽きとめた。
The inventors of the present invention have conducted investigations, experiments and analyzes and found that in the rapid start type fluorescent lamp, the tendency of the fluorescent substance to be charged is closely related to the yellowing of the fluorescent substance and the blackening of the EC film. I did what I was doing.

【0011】すなわち、ラピッドスタ−ト形けい光ラン
プの3波長発光形けい光体としては、赤色系けい光体と
してY2 O3 :Eu、青色系けい光体としてBaMg2
Al1627:Eu、緑色系けい光体として(Ra,T
b,Ce)・(P,Si)O4が多用されている。
[0011] That is, rapid Star - The three-wavelength emission type phosphor bet type fluorescent lamps, as red phosphors Y2 O3: Eu, BaMg 2 as blue phosphors
Al 16 O 27 : Eu, as a green phosphor (Ra, T
b, Ce) · (P, Si) O 4 is often used.

【0012】このようなけい光体について帯電傾向と黒
化の発生具合を調べてみた。帯電傾向は通常知られてい
るように、粒子径44〜74μmの還元鉄粉との接触時
にけい光体1g当りの帯電電荷量で示される。図2にお
いては、けい光体の帯電傾向と、点灯500時間後にお
けるけい光体への水銀および水銀化合物の吸着量を示
す。この実験では、けい光体としては赤色けい光体Y2
O3:Euを用い、けい光体粒子の表面に金属酸化物の
粉末を付着させる方法で帯電傾向を変化させた。
The charging tendency and the occurrence of blackening were investigated for such a phosphor. As is generally known, the charging tendency is indicated by the amount of charged electric charge per 1 g of the fluorescent substance when contacting with the reduced iron powder having a particle diameter of 44 to 74 μm. FIG. 2 shows the charging tendency of the phosphor and the adsorption amounts of mercury and a mercury compound on the phosphor after 500 hours of lighting. In this experiment, the red phosphor Y2 is used as the phosphor.
Using O3: Eu, the electrification tendency was changed by the method of depositing the metal oxide powder on the surface of the phosphor particles.

【0013】上記図2の特性から、水銀および水銀化合
物のけい光体に対する吸着性は、けい光体の帯電傾向に
依存していることが判明した。そして、けい光体の帯電
傾向が0〜+1μC/gの範囲で水銀および水銀化合物
のけい光体に対する吸着量が最小となり、これ以下およ
び以上のいづれに変化しても水銀および水銀化合物の吸
着量は増加する。
From the characteristics shown in FIG. 2, it was found that the adsorptivity of mercury and mercury compounds to the phosphor depends on the charging tendency of the phosphor. When the charging tendency of the phosphor is in the range of 0 to +1 μC / g, the adsorption amount of mercury and a mercury compound on the phosphor becomes the minimum, and the adsorption amount of mercury and a mercury compound is changed to less than this value or above. Will increase.

【0014】なお、けい光体の帯電傾向は金属酸化物の
種類により正の方向に帯電したり、負の方向に帯電する
ことが判り、MgOはけい光体を正の方向に帯電させる
とともに、SiO2 はけい光体を負の方向に帯電させる
傾向がある。
It has been found that the charging tendency of the phosphor is positively charged or negatively charged depending on the type of the metal oxide, and MgO charges the phosphor in the positive direction and at the same time, SiO 2 tends to charge the phosphor in the negative direction.

【0015】そして、Mgに代わって、Ca、Sr、B
a、Znの各酸化物の中から選ばれた1種の金属酸化物
を用いてもけい光体の帯電傾向を正の方向に変化させる
ことができる。
And instead of Mg, Ca, Sr, B
Even if one kind of metal oxide selected from the oxides of a and Zn is used, the charging tendency of the phosphor can be changed in the positive direction.

【0016】また、SiO2 に代わって、Sn、Ti、
Ge、Ta、Nb、V、Moの各酸化物の中から選ばれ
た少なくとも一種を用いてもけい光体の帯電傾向を負の
方向に変化させることができる。
In addition, instead of SiO 2 , Sn, Ti,
The charge tendency of the phosphor can be changed in the negative direction by using at least one selected from the oxides of Ge, Ta, Nb, V, and Mo.

【0017】さらに、これら酸化物は、けい光体に対し
て0.01〜3.0重量%の範囲で付着させれば有効で
ある。つまり、けい光体における帯電傾向の制御は金属
酸化物の量が非常に重要な因子となっており、付着量が
3.0重量%より多くなると、各けい光体の発光出力が
著しく低下する。一方、付着量が0.01重量%よりす
くなくなると、金属酸化物を付着させる効果、つまり帯
電傾向を変える作用が顕著でなくなる。
Further, it is effective if these oxides are deposited in the range of 0.01 to 3.0% by weight with respect to the phosphor. In other words, the amount of metal oxide is a very important factor for controlling the charging tendency of the phosphor, and when the amount of attachment is more than 3.0% by weight, the emission output of each phosphor remarkably decreases. .. On the other hand, when the adhesion amount is less than 0.01% by weight, the effect of adhering the metal oxide, that is, the effect of changing the charging tendency is not remarkable.

【0018】一方、図3は、各種の帯電傾向をもつけい
光体を20W直管形ラピッドスタート形けい光ランプの
EC膜の上に塗布して3000時間点灯後のEC膜黒化
発生率を測定したものである。図3の特性Aは、EC膜
の抵抗値が0.50KΩ/cmの場合である。
On the other hand, FIG. 3 shows the rate of occurrence of blackening of the EC film after lighting for 3000 hours by coating the photoconductors having various charging tendencies on the EC film of a 20 W straight tube type rapid start type fluorescent lamp. It was measured. Characteristic A in FIG. 3 is the case where the resistance value of the EC film is 0.50 KΩ / cm.

【0019】図3の特性から、EC膜黒化発生率をはけ
い光体の帯電傾向に左右されることが判り、図2に示し
た水銀および水銀化合物のけい光体に対する吸着性と対
応していることが明らかになった。
From the characteristics of FIG. 3, it was found that the EC film blackening occurrence rate depends on the charging tendency of the phosphor, which corresponds to the adsorptivity of mercury and mercury compounds to the phosphor shown in FIG. It became clear.

【0020】そして、けい光体の帯電電荷量が−1μC
/g以下の領域では、帯電傾向の負の値が増す程EC膜
黒化の発生率が高くなる。また、けい光体の帯電電荷量
が+2μC/g以上の領域でもEC膜黒化が発生してい
る。けい光体の帯電電荷量が−0.5〜+1.5μC/
gの範囲では、点灯3000時間後でもEC膜黒化の発
生は皆無であった。そして、この場合周囲温度が0℃の
低温始動試験を行ったが、格別な始動電圧の上昇がな
く、始動特性に異常は認められなかった。
The amount of charge on the phosphor is -1 μC.
In the range of / g or less, the rate of EC film blackening increases as the negative value of the charging tendency increases. Further, EC film blackening occurs even in a region where the amount of charge of the phosphor is +2 μC / g or more. The amount of charge on the phosphor is -0.5 to +1.5 μC /
Within the range of g, no blackening of the EC film was observed even after 3000 hours of lighting. Then, in this case, a low temperature starting test was conducted at an ambient temperature of 0 ° C., but there was no particular increase in the starting voltage, and no abnormality was found in the starting characteristics.

【0021】図3における特性Bは、EC膜の抵抗値を
1.0KΩ/cmとした場合のEC膜黒化発生率を測定し
たものである。この場合はEC膜の抵抗値が大きいので
けい光体被膜を挟んでEC膜と水銀との電位差が小さ
く、けい光体被膜の絶縁破壊が少なくなるため、EC膜
の黒化発生はかなり改善されることが認められるが、始
動電圧が高くなり、0℃の低温始動の場合に確実な始動
が不可能となり、始動特性に異常が生じる。このため、
EC膜の抵抗値は0.9KΩ/cm以下で、0.1KΩ/
cm以上がよい。
Characteristic B in FIG. 3 is a measurement of the EC film blackening occurrence rate when the resistance value of the EC film is 1.0 KΩ / cm. In this case, since the resistance value of the EC film is large, the potential difference between the EC film and mercury is small across the phosphor film, and the dielectric breakdown of the phosphor film is reduced, so that the blackening of the EC film is considerably improved. Although it is recognized that the starting voltage becomes high, reliable starting becomes impossible in the case of low temperature starting at 0 ° C., and the starting characteristic becomes abnormal. For this reason,
The resistance value of EC film is 0.9 KΩ / cm or less, 0.1 KΩ / cm
cm or more is good.

【0022】[0022]

【実施例】以下本発明について、図1に示す一実施例に
もとづき説明する。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below with reference to an embodiment shown in FIG.

【0023】図面は20Wの直管形ラピッドスタート形
けい光ランプを示し、1はガラスバルブである。バルブ
1の両端はフレアステム2、2により気密に閉塞されて
おり、これらステム2、2にはそれぞれ一対のリード線
3…が気密に貫通されている。
The drawing shows a 20 W straight tube type rapid start type fluorescent lamp, and 1 is a glass bulb. Both ends of the valve 1 are airtightly closed by flare stems 2 and 2, and a pair of lead wires 3 ...

【0024】両ステム2、2の各リード線3、3間には
タングステン等からなる熱陰極、すなわちフィラメント
4、4が掛け渡されている。なお、フィラメント4、4
には図示しないが酸化バリウムなどの電子放射物質が塗
布されている。
A hot cathode made of tungsten or the like, that is, filaments 4 and 4 are provided between the lead wires 3 and 3 of both the stems 2 and 2. The filaments 4, 4
Although not shown in the drawing, an electron emitting substance such as barium oxide is applied.

【0025】上記バルブ1の内面には、酸化錫などのよ
うな透明性導電膜(EC膜=ネサ膜)5が形成されてお
り、この透明性導電膜5の表面にはけい光体被膜6が形
成されている。このけい光体被膜6は3波長発光形希土
類けい光体を用いており、赤色系けい光体にはY
2 3 :Eu(赤色)、青色系けい光体にはBaMg2
Al1627:Eu、および緑色けい光体には(Re,T
b,Ce)・(P,Si)O4 が用いられ、これら3種
のけい光体粉末を混合して構成されている。これらけい
光体は、図1の(B)図に示すように、けい光体粉末1
0の表面に金属酸化物粉末を付着させることにより帯電
傾向を変化させてある。
A transparent conductive film (EC film = nesa film) 5 such as tin oxide is formed on the inner surface of the bulb 1, and the phosphor film 6 is formed on the surface of the transparent conductive film 5. Are formed. This phosphor coating 6 uses a three-wavelength emitting rare earth phosphor, and Y is used for the red phosphor.
2 O 3 : Eu (red), BaMg 2 for blue phosphor
Al 16 O 27 : Eu, and (Re, T
b, Ce) · (P, Si) O 4 is used, is constructed by mixing these three phosphor powder. As shown in FIG. 1B, these phosphors are phosphor powders 1
The charge tendency is changed by adhering the metal oxide powder to the surface of No. 0.

【0026】つまり、これらけい光体は、金属酸化物の
種類および付着量を適宜に選択して、けい光体全体の帯
電電荷量が、−0.5〜+1.5μC/gの範囲に制御
されている。また、EC膜5は電気抵抗値が0.1〜
0.9KΩ/cmに設定されている。そして、バルブ1内
には、所定量の水銀と、アルゴン等の希ガスが封入され
ている。このような構成のけい光ランプは、点灯300
0時間を経過しても、けい光体の黄変および黒化の発生
は認められない。
That is, in these phosphors, the kind and the amount of the metal oxide are appropriately selected to control the charge amount of the whole phosphor within the range of -0.5 to +1.5 μC / g. Has been done. Further, the EC film 5 has an electric resistance value of 0.1 to 0.1.
It is set to 0.9 KΩ / cm. The bulb 1 is filled with a predetermined amount of mercury and a rare gas such as argon. The fluorescent lamp having such a configuration is lit up 300
Even after 0 hour, no yellowing or blackening of the phosphor is observed.

【0027】これは、けい光体の帯電電荷量を−0.5
〜+1.5μC/gの範囲に規制したので、けい光体が
水銀原子や不純物との反応による水銀化合物の吸着性が
弱めれれ、これら水銀原子や水銀化合物がけい光体から
離れ易くなったために、けい光体の黄変やEC膜の黒化
を防止するものと推測される。
This means that the amount of charge on the phosphor is -0.5.
Since it is regulated within the range of to +1.5 μC / g, the adsorbability of the mercury compound is weakened by the reaction of the phosphor with the mercury atom and impurities, and the mercury atom and the mercury compound are easily separated from the phosphor. It is presumed that it prevents yellowing of the phosphor and blackening of the EC film.

【0028】なお、始動電圧を下げるために、けい光体
にα−アルミナ(Al2 3 )を混合させると、α−ア
ルミナは外部から格別な刺激を付与しなくても電子放射
性がよいので、始動電圧を引き下げることができる。な
お、本発明は3波長発光形けい光体を用いることに限ら
ず、従来のさらに、本発明は直管形けい光ランプに限ら
ず、環形、コンパクト屈曲形などのランプに適用可能で
ある。
When the phosphor is mixed with α-alumina (Al 2 O 3 ) in order to lower the starting voltage, α-alumina has a good electron emission property even if no external stimulus is applied. , The starting voltage can be lowered. The present invention is not limited to the use of a three-wavelength emission type phosphor, and the present invention is applicable not only to a straight tube type fluorescent lamp but also to a ring type lamp, a compact bent type lamp or the like.

【0029】[0029]

【発明の効果】以上説明したように本発明によれば、け
い光体の帯電傾向を制御することにより、けい光体と水
銀および水銀化合物の吸着性を規制することができ、け
い光体の黄変やEC膜の黒化を防止することができる。
As described above, according to the present invention, by controlling the charging tendency of the phosphor, the adsorbability of the phosphor and mercury and mercury compounds can be regulated, and the phosphor can be controlled. It is possible to prevent yellowing and blackening of the EC film.

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

【図1】本発明の一実施例を示し、(A)図はラピッド
スタ−ト形けい光ランプの断面図、(B)図はけい光体
粉末の表面にMgO粉末を付着した状態を示す模式図。
1 shows an embodiment of the present invention, FIG. 1 (A) is a sectional view of a rapid start type fluorescent lamp, and FIG. 1 (B) is a state in which MgO powder is adhered to the surface of phosphor powder. Pattern diagram.

【図2】けい光体の帯電傾向と水銀および水銀化合物の
吸着量との関係を示す図。
FIG. 2 is a diagram showing a relationship between a charging tendency of a phosphor and an adsorption amount of mercury and a mercury compound.

【図3】けい光体の帯電傾向とEC膜黒化発生率との関
係を示す図。
FIG. 3 is a diagram showing a relationship between a charging tendency of a phosphor and an EC film blackening occurrence rate.

【符号の説明】[Explanation of symbols]

1…バルブ、2…ステム、3…リード線、4…電極、5
…EC膜、6…けい光体被膜、10…けい光体、20…
金属酸化物粉末。
1 ... Valve, 2 ... Stem, 3 ... Lead wire, 4 ... Electrode, 5
… EC film, 6… Fluorescent film, 10… Fluorescent material, 20…
Metal oxide powder.

フロントページの続き (72)発明者 長澤 公義 東京都港区三田一丁目4番28号 東芝ライ テツク株式会社内 (72)発明者 玉谷 正昭 神奈川県川崎市幸区小向東芝町1番地 株 式会社東芝総合研究所内 (72)発明者 寺島 賢二 神奈川県横浜市磯子区新杉田町8番地 株 式会社東芝横浜事業所内Front Page Continuation (72) Inventor, Kimiyoshi Nagasawa 1-4-2-4 Mita, Minato-ku, Tokyo Within Toshiba Lighting & Technology Co., Ltd. (72) Inventor Kenji Terashima 8 Shinsita-cho, Isogo-ku, Yokohama-shi, Kanagawa Incorporated company Toshiba Yokohama Office

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 バルブの内面に透明性導電膜およびけい
光体層を形成し、このバルブ内に水銀および希ガスを封
入したラピッドスタ−ト形けい光ランプにおいて、 前記けい光体層を構成するけい光体は、粒子径74〜4
4μmの還元鉄粉との接触時にけい光体1g当り−0.
5〜+1.5マイクロク−ロンの電荷を帯電したことを
特徴とするラピッドスタ−ト形けい光ランプ。
1. A rapid-start type fluorescent lamp in which a transparent conductive film and a phosphor layer are formed on the inner surface of a bulb, and mercury and a rare gas are enclosed in the bulb, wherein the phosphor layer is formed. The fluorescent substance has a particle diameter of 74 to 4
When contacting with 4 μm of reduced iron powder, −0.
A rapid start type fluorescent lamp characterized by being charged with an electric charge of 5 to +1.5 micro coulombs.
【請求項2】 上記けい光体は、金属酸化物の粒子を
0.01〜3.0重量%の割合で付着させることによ
り、けい光体1g当り−0.5〜+1.5マイクロク−
ロンの電荷を帯電したことを特徴とする請求項1に記載
のラピッドスタ−ト形けい光ランプ。
2. The phosphor described above, wherein particles of a metal oxide are adhered in a proportion of 0.01 to 3.0% by weight, whereby the phosphor has a concentration of −0.5 to +1.5 μg / g per 1 g of the phosphor.
2. The rapid-start type fluorescent lamp according to claim 1, which is charged with Ron's electric charge.
【請求項3】 上記金属酸化物の粒子は、MgOである
ことを特徴と請求項2に記載のラピッドスタ−ト形けい
光ランプ。
3. The rapid start type fluorescent lamp according to claim 2, wherein the metal oxide particles are MgO.
【請求項4】 上記透明性導電膜は、電気抵抗値が0.
1〜0.9KΩ/cmであることを特徴とする請求項1な
いし請求項3のいづれかに記載のラピッドスタ−ト形け
い光ランプ。
4. The transparent conductive film has an electric resistance value of 0.
The rapid start type fluorescent lamp according to any one of claims 1 to 3, characterized in that it is 1 to 0.9 KΩ / cm.
JP19146691A 1991-07-31 1991-07-31 Rapid start fluorescent lamp Expired - Lifetime JP3343362B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19146691A JP3343362B2 (en) 1991-07-31 1991-07-31 Rapid start fluorescent lamp

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19146691A JP3343362B2 (en) 1991-07-31 1991-07-31 Rapid start fluorescent lamp

Publications (2)

Publication Number Publication Date
JPH0536381A true JPH0536381A (en) 1993-02-12
JP3343362B2 JP3343362B2 (en) 2002-11-11

Family

ID=16275124

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19146691A Expired - Lifetime JP3343362B2 (en) 1991-07-31 1991-07-31 Rapid start fluorescent lamp

Country Status (1)

Country Link
JP (1) JP3343362B2 (en)

Also Published As

Publication number Publication date
JP3343362B2 (en) 2002-11-11

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