JPH0140458B2 - - Google Patents
Info
- Publication number
- JPH0140458B2 JPH0140458B2 JP56009930A JP993081A JPH0140458B2 JP H0140458 B2 JPH0140458 B2 JP H0140458B2 JP 56009930 A JP56009930 A JP 56009930A JP 993081 A JP993081 A JP 993081A JP H0140458 B2 JPH0140458 B2 JP H0140458B2
- Authority
- JP
- Japan
- Prior art keywords
- phosphor
- boric acid
- phosphor layer
- aqueous solution
- bulb
- 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
Links
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 41
- 239000000843 powder Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 12
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 10
- 239000004327 boric acid Substances 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 239000011521 glass Substances 0.000 claims description 5
- 239000003595 mist Substances 0.000 claims description 2
- 238000001179 sorption measurement Methods 0.000 claims description 2
- 238000007664 blowing Methods 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 238000000576 coating method Methods 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 6
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 229910052810 boron oxide Inorganic materials 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 2
- 230000005611 electricity Effects 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
- 238000002156 mixing Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- XBJJRSFLZVLCSE-UHFFFAOYSA-N barium(2+);diborate Chemical compound [Ba+2].[Ba+2].[Ba+2].[O-]B([O-])[O-].[O-]B([O-])[O-] XBJJRSFLZVLCSE-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- -1 manganese-activated calcium Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 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
- H01J61/38—Devices for influencing the colour or wavelength of the light
- H01J61/42—Devices for influencing the colour or wavelength of the light by transforming the wavelength of the light by luminescence
- H01J61/46—Devices characterised by the binder or other non-luminescent constituent of the luminescent material, e.g. for obtaining desired pouring or drying properties
Landscapes
- Formation Of Various Coating Films On Cathode Ray Tubes And Lamps (AREA)
Description
【発明の詳細な説明】
本発明は蛍光ランプ、水銀ランプ等のバルブ内
面に蛍光体層を形成する方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for forming a phosphor layer on the inner surface of a bulb of a fluorescent lamp, mercury lamp, or the like.
従来、蛍光ランプ、水銀ランプ等のガラスバル
ブ内面に蛍光体層を形成するには、まず有機バイ
ンダーを水又は有機溶剤に溶解したラツカー中
に、蛍光体及び蛍光体被着剤の粉末を分散させて
蛍光体塗液を調合し、これをバルブ内面に塗布し
溶剤を乾燥させて蛍光体塗膜を形成した後、焼成
して塗膜中に残存している有機バインダーを焼去
する方法が行われている。しかしこの様な従来の
方法は、乾燥工程と焼成工程に多大な設備を要
し、又膨大な熱エネルギーを必要とすることが問
題となつている。 Conventionally, in order to form a phosphor layer on the inner surface of a glass bulb such as a fluorescent lamp or mercury lamp, the phosphor and phosphor adhesive powder are first dispersed in a lacquer in which an organic binder is dissolved in water or an organic solvent. The method is to prepare a phosphor coating liquid, apply it to the inner surface of the bulb, dry the solvent, form a phosphor coating, and then sinter it to burn off the organic binder remaining in the coating. It is being said. However, such conventional methods require a large amount of equipment for the drying process and the firing process, and there are problems in that they require a huge amount of thermal energy.
この問題を解消し蛍光ランプ等の製造工程の省
エネルギー化を目的として、近年、蛍光体粉末を
静電気を利用して塗着させるいわゆる静電粉体塗
装方法が種々研究されている。この方法は、(1)蛍
光体粉末を直接塗着させる方法のため塗液調合工
程が不要、(2)溶剤を使用しないため乾燥工程が不
要、(3)有機バインダーを使用しないため焼成工程
が不要等の利点があるが、その反面溶剤方式に比
べて蛍光体の被着力が弱いという欠点がある。 In order to solve this problem and save energy in the manufacturing process of fluorescent lamps and the like, various so-called electrostatic powder coating methods have been studied in recent years, in which phosphor powder is applied using static electricity. This method (1) does not require a coating liquid preparation process because it directly applies the phosphor powder, (2) does not require a drying process because it does not use a solvent, and (3) does not require a baking process because it does not use an organic binder. It has the advantage that it is unnecessary, but on the other hand, it has the disadvantage that the adhesion of the phosphor is weaker than that of the solvent method.
一方、一般に蛍光ランプ等に使用される蛍光体
粉末は平均粒径が5〜10μとかなり大きく、しか
も比重が3〜5と大きいためガラス表面に蛍光体
層を形成させた後に、衝撃、振動等で脱落しやす
い傾向がある。従つて通常被着力を増強させる目
的で、例えば酸化アルミニウム微粉末、あるいは
硼酸バリウム等の無機物を蛍光体粉末に混入して
蛍光体層を形成している。ところが溶剤方式の場
合には塗液調合工程での撹拌で蛍光体と蛍光体被
着剤の混合は充分均一に行えるが、粉体塗装方式
の場合は粉体どうしの混合になるため均一な混合
が難しく、又均一に混合されたとしても塗着させ
る時の空気流の移送によつて蛍光体と被着剤の分
離が起りやすいため、形成された蛍光体層は蛍光
体被着剤の混入濃度が不均一になり、充分な被着
強度が得られず、従つて溶剤方式に比べて被着力
の低下はさけられない。 On the other hand, phosphor powders generally used in fluorescent lamps have a fairly large average particle size of 5 to 10 microns, and have a high specific gravity of 3 to 5. It tends to fall off easily. Therefore, for the purpose of increasing adhesion, a phosphor layer is usually formed by mixing an inorganic substance such as fine aluminum oxide powder or barium borate into phosphor powder. However, in the case of a solvent coating method, the phosphor and the phosphor adhesive can be mixed sufficiently uniformly by stirring during the coating liquid preparation process, but in the case of a powder coating method, the powders are mixed together, so it is difficult to achieve uniform mixing. Even if they are mixed uniformly, the phosphor and adhesive tend to separate due to the transport of air flow during coating, so the formed phosphor layer is free from contamination with the phosphor adhesive. The concentration becomes non-uniform and sufficient adhesion strength cannot be obtained, so a decrease in adhesion strength compared to the solvent method is unavoidable.
本発明は上記の欠点を改良するためになされた
もので、静電粉体塗装方式で充分な被着強度を有
する蛍光体層を形成する方法を提供することを目
的としたものである。 The present invention has been made to improve the above-mentioned drawbacks, and aims to provide a method for forming a phosphor layer having sufficient adhesion strength using an electrostatic powder coating method.
本発明は、蛍光体粉末を荷電させてバルブ内面
に塗着させた後、この蛍光体層に硼酸水溶液を霧
状にして吹き付け、続いてバルブを加熱して蛍光
体層中の水分を除去するようにしたことを特徴と
するものである。 In the present invention, after charging the phosphor powder and applying it to the inner surface of the bulb, a boric acid aqueous solution is sprayed onto the phosphor layer in the form of a mist, and then the bulb is heated to remove moisture in the phosphor layer. It is characterized by the following.
以下本発明を実施例にもとづいて説明する。 The present invention will be explained below based on examples.
アンチモン、マンガン付活ハロリン酸カルシウ
ム蛍光体を70KVの電圧を印加した静電粉体塗装
ノズルから噴射させ、32mmφの20W蛍光ランプ用
バルブ内面に塗着させる。次に濃度3重量%の硼
酸水溶液を超音波霧発生装置で霧状にし前記バル
ブ内に吹込み塗着している蛍光体に付着させる。
付着した硼酸水溶液は積層となつている蛍光体粒
子間に毛細管現象で浸み込み塗着している蛍光体
全体に均一に吸着される。なお硼酸水の吹込み量
は、バルブ1本当り0.3c.c.に調整する。次にバル
ブを約400℃に加熱し蛍光体に吸着した水分を除
去する。この工程で蛍光体粒子表面に吸着してい
る硼酸は脱水され無水硼酸(酸化硼素)になり、
その過程で熔融して蛍光体粒子間、及び蛍光体と
ガラス表面の被着力を強固にする。 Antimony and manganese-activated calcium halophosphate phosphor is sprayed from an electrostatic powder coating nozzle to which a voltage of 70KV is applied, and coated on the inner surface of a 32mmφ 20W fluorescent lamp bulb. Next, a boric acid aqueous solution having a concentration of 3% by weight is atomized using an ultrasonic atomizer and is blown into the bulb to adhere to the phosphor coated thereon.
The attached boric acid aqueous solution penetrates between the laminated phosphor particles by capillary action and is uniformly adsorbed onto the entire coated phosphor. The amount of boric acid injected should be adjusted to 0.3cc per bulb. Next, the bulb is heated to about 400°C to remove the moisture adsorbed on the phosphor. In this process, the boric acid adsorbed on the surface of the phosphor particles is dehydrated and becomes boric anhydride (boron oxide).
In the process, it melts and strengthens the adhesion between the phosphor particles and between the phosphor and the glass surface.
このようにして得られた蛍光体層は従来の溶剤
方式で形成した蛍光体層と同等の被着強度が得ら
れた。なお前記実施例において被着強度と硼酸水
溶液の濃度及び吸着させる量には相関があり、濃
度の高い程、又吸着量の多い程被着強度は向上す
るが、本来蛍光体層の被着力増強剤の添加は蛍光
体の発光効率に対してマイナスの要因にこそな
れ、プラスになることはないので、その添加量は
最低必要量におさえるべきものである。本発明に
おいては硼酸(最終的には酸化硼素の形になる)
が蛍光体被着力増強剤として作用しているが、そ
の量は前記実施例程度、すなわち蛍光体に対して
最終的に残留する酸化硼素の量が約0.3重量%程
度が適当である。 The phosphor layer thus obtained had adhesion strength equivalent to that of a phosphor layer formed by a conventional solvent method. In the above examples, there is a correlation between the adhesion strength, the concentration of the boric acid aqueous solution, and the adsorbed amount, and the higher the concentration and the larger the adsorption amount, the better the adhesion strength. Since the addition of an agent can only be a negative factor for the luminous efficiency of the phosphor and not a positive factor, the amount added should be kept to the minimum necessary amount. In the present invention, boric acid (finally in the form of boron oxide)
The amount of boron oxide acting as a phosphor adhesion enhancer is approximately the same as in the above example, that is, the amount of boron oxide ultimately remaining in the phosphor is approximately 0.3% by weight.
以上述べたように本発明は、静電的に塗着され
た蛍光体層上に超音波霧発生装置によつて霧状化
された硼酸水溶液を吹き付け、この後蛍光体層中
の水分を除去したものであるから、静電気を利用
した粉体塗装方式のものであつても、充分な被着
強度を有する蛍光体層を形成できる効果を奏す
る。 As described above, the present invention sprays a boric acid aqueous solution atomized by an ultrasonic fog generator onto a phosphor layer applied electrostatically, and then removes water in the phosphor layer. Therefore, it is possible to form a phosphor layer with sufficient adhesion strength even when using a powder coating method using static electricity.
Claims (1)
的に塗着させる工程と、該ガラス管内に硼酸水溶
液を超音波霧発生装置によつて霧状にして吹込み
その硼酸水溶液を蛍光体に吸着させる工程と、次
いでガラス管を加熱し蛍光体層中の水分を除去す
る工程とを有することを特徴とする蛍光体層の形
成方法。1. A step of electrostatically applying a charged phosphor powder to the inner surface of a glass tube, and blowing a boric acid aqueous solution into the glass tube in the form of a mist using an ultrasonic fog generator, and turning the boric acid aqueous solution into a phosphor. A method for forming a phosphor layer, comprising the steps of adsorption, and then heating a glass tube to remove moisture in the phosphor layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP993081A JPS57124829A (en) | 1981-01-26 | 1981-01-26 | Formation of phosphor layer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP993081A JPS57124829A (en) | 1981-01-26 | 1981-01-26 | Formation of phosphor layer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57124829A JPS57124829A (en) | 1982-08-03 |
JPH0140458B2 true JPH0140458B2 (en) | 1989-08-29 |
Family
ID=11733776
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP993081A Granted JPS57124829A (en) | 1981-01-26 | 1981-01-26 | Formation of phosphor layer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57124829A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59149648A (en) * | 1983-02-04 | 1984-08-27 | Toshiba Corp | High-pressure discharge lamp |
US4914346A (en) * | 1983-03-04 | 1990-04-03 | Gte Products Corporation | Lamp envelope having a luminescent material on the interior surface thereof, method of applying said material, and material to be applied |
CA1271371A (en) * | 1983-03-04 | 1990-07-10 | Gte Products Corporation | Lamp envelope having an interior coating of luminescent material and boric oxide |
JPS6174237A (en) * | 1984-09-19 | 1986-04-16 | Mitsubishi Electric Corp | Formation of powder film on inner surface of tubular bulb |
US4597984A (en) * | 1985-06-03 | 1986-07-01 | General Electric Company | Method and apparatus for coating fluorescent lamp tubes |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5182979A (en) * | 1975-01-17 | 1976-07-21 | Hitachi Ltd | KANKYUNOSEI DENTO SOHOHO |
-
1981
- 1981-01-26 JP JP993081A patent/JPS57124829A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5182979A (en) * | 1975-01-17 | 1976-07-21 | Hitachi Ltd | KANKYUNOSEI DENTO SOHOHO |
Also Published As
Publication number | Publication date |
---|---|
JPS57124829A (en) | 1982-08-03 |
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