JPH0574188B2 - - Google Patents
Info
- Publication number
- JPH0574188B2 JPH0574188B2 JP10452784A JP10452784A JPH0574188B2 JP H0574188 B2 JPH0574188 B2 JP H0574188B2 JP 10452784 A JP10452784 A JP 10452784A JP 10452784 A JP10452784 A JP 10452784A JP H0574188 B2 JPH0574188 B2 JP H0574188B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- alumina
- resistance
- tube
- phosphor
- 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
Links
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 23
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 17
- 239000011248 coating agent Substances 0.000 claims description 10
- 238000000576 coating method Methods 0.000 claims description 10
- 239000011521 glass Substances 0.000 claims description 10
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 8
- 150000002910 rare earth metals Chemical class 0.000 claims description 8
- 229910052743 krypton Inorganic materials 0.000 claims description 3
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 claims description 3
- CMSGUKVDXXTJDQ-UHFFFAOYSA-N 4-(2-naphthalen-1-ylethylamino)-4-oxobutanoic acid Chemical compound C1=CC=C2C(CCNC(=O)CCC(=O)O)=CC=CC2=C1 CMSGUKVDXXTJDQ-UHFFFAOYSA-N 0.000 description 11
- 238000011109 contamination Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 230000004907 flux Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J61/00—Gas-discharge or vapour-discharge lamps
- H01J61/02—Details
- H01J61/30—Vessels; Containers
- H01J61/35—Vessels; Containers provided with coatings on the walls thereof; Selection of materials for the coatings
Landscapes
- Discharge Lamps And Accessories Thereof (AREA)
- Vessels And Coating Films For Discharge Lamps (AREA)
Description
【発明の詳細な説明】
〔発明の利用分野〕
本発明は内面に導電被膜を形成した省電力形の
ラピツドスタート形蛍光ランプに関し、特に希土
類蛍光体を使用したこの種ランプの改良に関する
ものである。[Detailed Description of the Invention] [Field of Application of the Invention] The present invention relates to a power-saving rapid-start type fluorescent lamp having a conductive coating formed on the inner surface thereof, and particularly relates to an improvement of this type of lamp using a rare earth phosphor. be.
従来のクリプトン(Kr)を主成分とするガス
を封入したラピツドスタート形の蛍光ランプに於
ては、起動性を改善するために内面導電被膜の抵
抗を低くしていた。そのためにHg汚れと称する
斑点状の外観不良の発生、導電膜の着色による光
束維持率の低下などの欠点があつた。この対策と
しては、特公昭45−26278号公報に記載のように
管端部の導電膜の抵抗を高くする方法が知られて
いるが、Krを主成分とする封入ガスで、特に希
土類蛍光体を使つた蛍光ランプでは、この方法で
は起動性が悪く実用に耐えなかつた。
In conventional rapid-start fluorescent lamps filled with a gas containing krypton (Kr) as the main component, the resistance of the inner conductive coating was lowered to improve start-up performance. This resulted in drawbacks such as the occurrence of spot-like appearance defects called Hg stains and a decrease in luminous flux maintenance rate due to coloring of the conductive film. As a countermeasure against this problem, a method is known to increase the resistance of the conductive film at the end of the tube, as described in Japanese Patent Publication No. 45-26278. This method had poor startup performance for fluorescent lamps using fluorophores, making it impractical.
したがつて、本発明の目的は上記欠点を解消し
たラピツドスタート形蛍光ランプを提供すること
にある。
SUMMARY OF THE INVENTION It is, therefore, an object of the present invention to provide a rapid-start fluorescent lamp which eliminates the above-mentioned drawbacks.
上記目的を達成するため本発明においては、
Hg汚れ及び導電膜着色対策として管端部のネサ
抵抗を上げ、これによつて従来は起動性が悪くな
つていたが、これを管内面にアルミナ薄膜を適当
量塗布し、蛍光膜の結着剤を変えることによつて
改善して実用に耐え得る省電力ラピツドスタート
形の高効率、高演色蛍光ランプを提供できるよう
にしたものである。
In order to achieve the above object, in the present invention,
As a countermeasure against Hg contamination and conductive film discoloration, the resistance at the end of the tube was increased, which conventionally resulted in poor startup performance. By changing the agent, it is possible to provide a power-saving, rapid-start, high-efficiency, high-color-rendering fluorescent lamp that can withstand practical use.
つまり、ガラス管内面に導電膜を形成し、その
上にアルミナを0.01〜0.1mg/cm2塗布すると起動
電圧(Vs)は約5%程度低下するが、これだけ
では実用上まで不充分であつた。一方、蛍光膜の
強度を上げるために添加される結着剤がVsに影
響を与えることがわかり、結着剤としての機能も
考え合わせ、アルフアアルミナが適当であること
がわかつた。蛍光体にアルフアアルミナを添加す
ると、導電膜の抵抗、特に管橋の抵抗を上げても
起動性が悪くならないことがわかつたものであ
る。 In other words, if a conductive film is formed on the inner surface of the glass tube and 0.01 to 0.1 mg/ cm2 of alumina is applied on it, the starting voltage (Vs) will be reduced by about 5%, but this alone is insufficient for practical use. . On the other hand, it was found that the binder added to increase the strength of the fluorescent film affected Vs, and considering its function as a binder, alpha alumina was found to be suitable. It has been found that when alpha alumina is added to the phosphor, starting performance does not deteriorate even if the resistance of the conductive film, especially the resistance of the tube bridge, is increased.
本発明の要旨は、ガラス管内面に導電被膜、ア
ルミナ被膜および蛍光体膜を形成し、前記ガラス
管内にクリプトンを含む希ガスを封入した蛍光ラ
ンプにおいて、前記ガラス管の管端部近傍におけ
る前記導電性被膜の抵抗値の平均値を30kΩ/cm2
以上とし、前記ガラス管の中央部における前記導
電性被膜の抵抗値の平均値を1kΩ/cm2以上
10kΩ/cm2以下とし、前記アルミナ被膜の被着量
を0.01mg/cm2以上0.1mg/cm2以下とし、前記蛍光
体膜には希土類蛍光体およびアルフアアルミナが
含まれていることを特徴とする蛍光ランプにあ
る。 The gist of the present invention is a fluorescent lamp in which a conductive film, an alumina film, and a phosphor film are formed on the inner surface of a glass tube, and a rare gas containing krypton is sealed in the glass tube. The average resistance value of the sexual membrane is 30kΩ/cm 2
or more, and the average value of the resistance value of the conductive coating at the center of the glass tube is 1 kΩ/cm 2 or more.
10 kΩ/cm 2 or less, the coating amount of the alumina film is 0.01 mg/cm 2 or more and 0.1 mg/cm 2 or less, and the phosphor film contains a rare earth phosphor and alpha alumina. There are fluorescent lamps.
以下本発明の一実施例を図により説明する。第
1図は本発明によるラピツドスタート形蛍光ラン
プの断面図を示し、ガラス管1の内面に酸化スズ
を主成分とした導電性被膜(以下ネサ膜と呼ぶ)
2を形成し、その上に平均粒径が100μm以下の
γアルミナから成るアルミナ保護膜3を形成し、
その上に蛍光膜4を形成する。蛍光膜4は希土類
蛍光体を主成分とし、その中にはVs低下と膜強
度向上とのために2重量%のαアルミナが添加さ
れている。管内には少量の水銀5と、Krを主成
分とする混合希ガス6が数mmHg封入される。こ
のような構成の40ワツト形ラピツドスタート蛍光
ランプで試験を行なつた。管外径32.5mm、ランプ
全長は約1200mmである。まず、第3図に示す管端
部A,Bの部分のネサ抵抗を10kΩ/cm2、中央部
1/3を5kΩ/cm2とし、蛍光体にはαアルミナを添
加しないランプで、アルミナ保護膜3の被着量を
変えて、起動電圧を調べた。その結果を第2図に
示す。アルミナ被着量が0.001mg/cm2ではアルミ
ナを塗布しない場合と起動電圧(Vs)は同等で
あるが、これらに比べて、0.01mg/cm2以上では約
5%Vsが低下する。しかし、アルミナ被着量が
0.1mg/cm2を超えると光束劣化、すなわち光束維
持率が悪くなつて来るので上限は0.1mg/cm2とす
るのが望ましい。次に、管中央部のネサ抵抗を約
10kΩ/cm2一定にし、管端部A,B共平均値が
10kΩ/cm2〜50kΩ/cm2の範囲で変えた。
An embodiment of the present invention will be described below with reference to the drawings. FIG. 1 shows a cross-sectional view of a rapid-start type fluorescent lamp according to the present invention, in which a conductive film (hereinafter referred to as NESA film) mainly composed of tin oxide is coated on the inner surface of a glass tube 1.
2 is formed, and an alumina protective film 3 made of γ alumina with an average particle size of 100 μm or less is formed thereon,
A fluorescent film 4 is formed thereon. The fluorescent film 4 is mainly composed of a rare earth phosphor, and 2% by weight of α-alumina is added therein to lower Vs and improve film strength. A small amount of mercury 5 and a few mmHg of a mixed rare gas 6 whose main component is Kr are sealed inside the tube. A test was conducted using a 40 watt Rapid Start fluorescent lamp constructed in this manner. The outer diameter of the tube is 32.5mm, and the total length of the lamp is approximately 1200mm. First, the resistance of the ends A and B of the tube shown in Fig. 3 is 10 kΩ/cm 2 , and the center 1/3 is 5 kΩ/cm 2 , and the lamp does not contain α-alumina to protect the alumina. The starting voltage was examined by varying the amount of film 3 deposited. The results are shown in FIG. When the alumina coating amount is 0.001 mg/cm 2 , the starting voltage (Vs) is the same as when no alumina is applied, but compared to these, when the alumina coating amount is 0.01 mg/cm 2 or more, Vs decreases by about 5%. However, the amount of alumina coating
If it exceeds 0.1 mg/cm 2 , the luminous flux will deteriorate, that is, the luminous flux maintenance rate will deteriorate, so it is desirable that the upper limit is 0.1 mg/cm 2 . Next, set the NESA resistance at the center of the tube to approximately
Keeping 10kΩ/ cm2 constant, the average value of tube ends A and B is
It was varied in the range of 10kΩ/cm 2 to 50kΩ/cm 2 .
Vsを第4図中の曲線C、Hg汚れ発生率を第5
図の曲線Eで示す。Vsは周囲温度が0℃のもの
で定格電圧を100%Vとして示してある。管端部
ネサ抵抗を10〜50kΩ/cm2の範囲で変えてもVsへ
の影響は2.5%V程度で、ほとんど影響しない。
一方、第5図よりネサ抵抗の平均値が30kΩ/cm2
以上でないとHg汚れが発生する。 Vs is curve C in Figure 4, and Hg staining incidence is curve 5.
This is shown by curve E in the figure. Vs is shown assuming that the ambient temperature is 0°C and the rated voltage is 100%V. Even if the tube end NESA resistance is changed in the range of 10 to 50 kΩ/cm 2 , the effect on Vs is about 2.5%V, which is almost no effect.
On the other hand, from Figure 5, the average value of Nesa resistance is 30kΩ/cm 2
Otherwise, Hg stains will occur.
ハロリン酸塩蛍光体のみであれば、10kΩ/cm2
程度以上あれば、Hg汚れの発生はほとんどない
が、少くとも希土類蛍光体を10%含む蛍光膜では
Hg汚れが出やすい。また、希土類蛍光体の含有
割合が増加するとVsも上昇してくる。このこと
から管全長の1/3に相当する管両端部のネサ抵抗
は平均30kΩ/cm2以上でなければならない。なお、
上記管端部の抵抗分布は管端に行くにしたがい順
次上昇するのが好ましい。 If only halophosphate phosphor is used, 10kΩ/cm 2
Hg contamination is unlikely to occur if it is above a certain level, but with a phosphor film that contains at least 10% rare earth phosphor,
Hg stains are likely to appear. Further, as the content ratio of the rare earth phosphor increases, Vs also increases. Therefore, the average resistance at both ends of the tube, which corresponds to 1/3 of the total length of the tube, must be 30 kΩ/cm 2 or more. In addition,
It is preferable that the resistance distribution at the tube end gradually increases toward the tube end.
次に、管両端場のネサ抵抗を約30kΩ/cm2一定
とし、中央部1/3の部分のネサ抵抗を0.3〜
20kΩ/cm2の範囲で変化させるとVsは第4図の曲
線D,Hg汚れ発生率は第5図Fのようになつた。 Next, the NESA resistance at both ends of the tube is set to be constant at approximately 30 kΩ/ cm2 , and the NESA resistance at the center 1/3 is set to 0.3~
When the resistance was changed within a range of 20 kΩ/cm 2 , Vs became as shown in curve D in Figure 4, and the Hg staining rate became as shown in Figure 5, F.
中央部の抵抗はVsに影響が大きく10kΩ/cm2以
下でなければ0℃でVsが定格電圧以上になり実
用にならない。一方、第5図曲線Fより、Hg汚
れは、1kΩ/cm2あれば発生しない。このことから
管中央部は1〜10kΩ/cm2が適当である。 The resistance in the center has a large effect on Vs, and unless it is less than 10kΩ/cm 2 , Vs will exceed the rated voltage at 0°C, making it impractical. On the other hand, from curve F in Figure 5, Hg contamination does not occur if it is 1 kΩ/cm 2 . From this, it is appropriate for the center part of the tube to have a resistance of 1 to 10 kΩ/cm 2 .
そして、蛍光体にαアルミナを添加するとVs
を低下させる効果があり、同時に、膜強度を上げ
ることができる。その添加量は1〜4重量%であ
ることが望ましい。その理由は1重量%未満であ
ると膜強度が弱くて実用的でなく、4重量%を超
えるとVsが飽和してくる上に光束が低下してき
てやはい実用的でないことによる。 And when alpha alumina is added to the phosphor, Vs
It has the effect of lowering the oxidation rate, and at the same time can increase the film strength. The amount added is preferably 1 to 4% by weight. The reason for this is that if it is less than 1% by weight, the film strength will be weak and is not practical, and if it exceeds 4% by weight, Vs will become saturated and the luminous flux will decrease, making it impractical.
以上説明した通り本発明はVsが高く、且つHg
汚れが発生し易い蛍光ランプ、即ち、蛍光体が10
%以上の希土類蛍光体を含み、封入ガスがKrを
主成分とするラピツドスタート形の蛍光ランプに
於てVsとHg汚れの両方を改善するため、アルミ
ナ保護膜、ネタ抵抗、蛍光膜への添加物等の仕様
を規制したものであり、本発明によりこの種の蛍
光ランプの始動性、点灯外観などの性能が向上で
きた。 As explained above, the present invention has high Vs and Hg
Fluorescent lamps that are prone to dirt, i.e. fluorescent lamps with 10%
In order to improve both Vs and Hg contamination in rapid-start type fluorescent lamps that contain % or more of rare earth phosphor and whose filler gas is mainly Kr, we have applied alumina protective film, net resistor, and fluorescent film to improve both Vs and Hg contamination. The specifications of additives, etc. are regulated, and the present invention has improved the performance of this type of fluorescent lamp, including its startability and lighting appearance.
以上述べた如く本発明によれば、従来始動性が
悪いために使用条件に制限があつたり、Hg汚れ
等の外観が多かつた希土類蛍光体を含むラピツド
スタート形の蛍光ランプの汎用化、性能向上が可
能となつた。
As described above, according to the present invention, rapid start type fluorescent lamps containing rare earth phosphors, which have conventionally had poor startability, limited usage conditions, and often had an appearance such as Hg stains, can be made more general. It became possible to improve performance.
従来ではHg汚れを防ぐためにネサ抵抗を高く
せざるを得ず、そうすればVsが高くなつて定格
電圧で点灯できないという問題があり実用化され
ていなかつたが、本発明ランプはこの矛盾を解決
したものであり、実用化が可能である。性能的に
は高演色、高効率(省電力)であり、照明経済上
の利点は大きい。 Conventionally, in order to prevent Hg contamination, the negative resistance had to be increased, which caused the problem that Vs would become high and the lamp could not be lit at the rated voltage, so it was not put to practical use.However, the lamp of the present invention resolves this contradiction. Therefore, it is possible to put it into practical use. In terms of performance, it has high color rendering and high efficiency (power saving), and has great advantages in terms of lighting economy.
第1図は本発明によるラピツドスタート形蛍光
ランプの断面図、第2図はアルミナ被着量とVs
の関係図、第3図は管の中央部と管端部とを説明
するための蛍光ランプ外観図、第4図はネサ抵抗
値とVsの関係を示す図、第5図はネサ抵抗値と
Hg汚れ発生率との関係を示す図である。
1……ガラス管、2……ネサ膜、3……アルミ
ナ保護膜、4……蛍光体膜、5……水銀、6……
封入ガス、曲線C……管端部ネサ抵抗とVsの関
係を示す曲線、曲線D……中央部ネサ抵抗とVs
の関係を示す曲線、曲線E……管端部ネサ抵抗と
Hg汚れ発生率の関係を示す曲線、曲線F……中
央部ネサ抵抗とHg汚れ発生率の関係を示す曲線。
Figure 1 is a cross-sectional view of a rapid start type fluorescent lamp according to the present invention, and Figure 2 shows the amount of alumina deposited and Vs.
Figure 3 is an external view of a fluorescent lamp to explain the center part of the tube and the tube ends, Figure 4 is a diagram showing the relationship between the NESA resistance value and Vs, and Figure 5 is a diagram showing the relationship between the NESA resistance value and Vs.
FIG. 3 is a diagram showing the relationship with Hg stain occurrence rate. 1... Glass tube, 2... Nesa film, 3... Alumina protective film, 4... Phosphor film, 5... Mercury, 6...
Filled gas, curve C...Curve showing the relationship between tube end NESA resistance and Vs, curve D...Central NESA resistance and Vs
Curve showing the relationship between curve E... tube end NESA resistance and
Curve showing the relationship between Hg stain occurrence rate, curve F...Curve showing the relationship between central NESA resistance and Hg stain occurrence rate.
Claims (1)
び蛍光体膜を形成し、前記ガラス管内にクリプト
ンを含む希ガスを封入した蛍光ランプにおいて、
前記ガラス管の管端部近傍における前記導電性被
膜の抵抗値の平均値を30kΩ/cm2以上とし、前記
ガラス管の中央部における前記導電性被膜の抵抗
値の平均値を1kΩ/cm2以上10kΩ/cm2以下とし、
前記アルミナ被膜の被着量を0.01mg/cm2以上0.1
mg/cm2以下とし、前記蛍光体膜には希土類蛍光体
およびアルフアアルミナが含まれていることを特
徴とする蛍光ランプ。 2 前記アルフアアルミナは前記蛍光体膜に対し
て1重量%以上4重量%以下添加されていること
を特徴とする特許請求の範囲第1項記載の蛍光ラ
ンプ。[Scope of Claims] 1. A fluorescent lamp in which a conductive film, an alumina film, and a phosphor film are formed on the inner surface of a glass tube, and a rare gas containing krypton is sealed in the glass tube,
The average value of the resistance value of the conductive coating near the tube end of the glass tube is 30 kΩ/cm 2 or more, and the average value of the resistance value of the conductive coating at the center of the glass tube is 1 kΩ/cm 2 or more. 10kΩ/ cm2 or less,
The coating amount of the alumina film should be 0.01 mg/cm 2 or more and 0.1
mg/cm 2 or less, and wherein the phosphor film contains a rare earth phosphor and alpha alumina. 2. The fluorescent lamp according to claim 1, wherein the alpha alumina is added in an amount of 1% by weight or more and 4% by weight or less with respect to the phosphor film.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10452784A JPS60249239A (en) | 1984-05-25 | 1984-05-25 | Rapid-state fluorescent lamp |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10452784A JPS60249239A (en) | 1984-05-25 | 1984-05-25 | Rapid-state fluorescent lamp |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60249239A JPS60249239A (en) | 1985-12-09 |
| JPH0574188B2 true JPH0574188B2 (en) | 1993-10-15 |
Family
ID=14382962
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10452784A Granted JPS60249239A (en) | 1984-05-25 | 1984-05-25 | Rapid-state fluorescent lamp |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60249239A (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5602444A (en) * | 1995-08-28 | 1997-02-11 | General Electric Company | Fluorescent lamp having ultraviolet reflecting layer |
| US5898265A (en) * | 1996-05-31 | 1999-04-27 | Philips Electronics North America Corporation | TCLP compliant fluorescent lamp |
| DE60300468T2 (en) * | 2002-06-19 | 2006-05-04 | Osram-Sylvania Inc., Danvers | Control of soluble mercury in fluorescent tubes |
| JP2009510673A (en) * | 2005-09-26 | 2009-03-12 | コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ | Low mercury consumption fluorescent lamp with phosphor / alumina coating layer |
| US20090079324A1 (en) * | 2007-09-20 | 2009-03-26 | Istvan Deme | Fluorescent lamp |
-
1984
- 1984-05-25 JP JP10452784A patent/JPS60249239A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60249239A (en) | 1985-12-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |