JPS603355B2 - Pigment coated europium activated yttrium oxysulfide phosphor - Google Patents
Pigment coated europium activated yttrium oxysulfide phosphorInfo
- Publication number
- JPS603355B2 JPS603355B2 JP13988977A JP13988977A JPS603355B2 JP S603355 B2 JPS603355 B2 JP S603355B2 JP 13988977 A JP13988977 A JP 13988977A JP 13988977 A JP13988977 A JP 13988977A JP S603355 B2 JPS603355 B2 JP S603355B2
- Authority
- JP
- Japan
- Prior art keywords
- light
- crab
- activated yttrium
- europium activated
- 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
Links
Landscapes
- Luminescent Compositions (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Description
【発明の詳細な説明】 本発明はカラーブラウン管用後光体に関する。[Detailed description of the invention] The present invention relates to a backlight for a color cathode ray tube.
従来カラーテレビにおいて、明かるし、外光のもとで画
面のコントラストをよくするためブラウン管前面におけ
る光の反射を少なくするいろいろな工夫が提案されてい
る。これらの工夫の中で、一般に前面ガラスパネルとし
て光透過率の小さいガラスを使用する。In conventional color televisions, various methods have been proposed to reduce the reflection of light on the front surface of the cathode ray tube in order to improve the brightness and contrast of the screen under external light. Among these measures, glass with low light transmittance is generally used as the front glass panel.
あるいは前面ガラスパネルのうち、姿光体層が塗布され
ていない部分を黒色にする、という2種類の方法が行わ
れている。しかし、前者は、蟹光体層が発した光に対す
る透過率も同時に小さくなってしまうので画面が暗くな
り、後者は、蟹光体層が塗布されていない部分の面積が
、全面積に占める割合が小さいため、外光の反射が充分
には減少しない「という欠点があった。Alternatively, there are two methods in which the portion of the front glass panel that is not coated with the photoluminescent layer is made black. However, in the former case, the transmittance of the light emitted by the crab phosphor layer also decreases, resulting in a dark screen, and in the latter case, the area where the crab phosphor layer is not coated is a proportion of the total area. Because of the small amount of light, the reflection of external light was not sufficiently reduced.
また、赤色顔料で被覆した赤色発光姿光体を備えたカラ
ーブラウン管が提案されている。Furthermore, a color cathode ray tube including a red light-emitting phosphor coated with a red pigment has been proposed.
このような構造のカラーブラウン管は外光のうち総光体
自体の発光色以外の色成分の反射を減少できるので、外
光の反射減少のためには、相当有効である。と考えられ
る。しかして現在まで赤色発光蟹光体、緑色発光蟹光体
、青色発光後光体にそれぞれ緑色青色顔料を被覆するこ
とが知られている。顔料を使用したブラウン管に於いて
は、コントラストの程度は顔料の分光反射率に強く依存
するため、顔料の選択が重要である。赤色顔料に於ては
、自然光で鮮かな赤色を示す物質例えばスルホセレン化
カドミウム、鉛母丹等が知られているが、毒性の点に於
てブラウン管に使用するのに適しない。A color cathode ray tube having such a structure can reduce the reflection of color components other than the emission color of the total light body itself, and is therefore quite effective in reducing the reflection of external light. it is conceivable that. Until now, it has been known to coat a red light-emitting crab light body, a green light-emitting crab light body, and a blue light-emitting halo body, respectively, with a green-blue pigment. In cathode ray tubes using pigments, the degree of contrast strongly depends on the spectral reflectance of the pigment, so the selection of the pigment is important. As for red pigments, substances such as cadmium sulfoselenide and lead matrix are known which exhibit a bright red color under natural light, but they are not suitable for use in cathode ray tubes due to their toxicity.
このため赤色顔料としてペンガラ(酸化鉄)が使用され
ているが、この物質では色の点に於て不充分であり、鮮
かな赤色をもち、しかも毒性のない顔料の開発が望まれ
てきた。本発明は、このような従来の問題を解決するた
めに行われたものであり、毒性のない、しかも従来の赤
色顔料に比し60触れ以上の波長の反射率の高い新赤色
顔料の硫化インジウムで被覆した赤色発光蟹光体を提供
しようとするものである。For this reason, pengara (iron oxide) is used as a red pigment, but this material is insufficient in terms of color, and there has been a desire to develop a pigment that has a bright red color and is not toxic. The present invention was made to solve these conventional problems, and uses indium sulfide, a new red pigment that is non-toxic and has a higher reflectance at wavelengths of 60 cm or more than conventional red pigments. The present invention aims to provide a red light-emitting crab luminous material coated with a red light emitting crab.
以下、本発明の実施例について詳述する。実施例 1
赤色発光姿光体のユーロピウム付活酸硫化イットリウム
(平均粒径が約7仏肌)25雌rを2500の‘の脱イ
オン水に懸濁させる。Examples of the present invention will be described in detail below. Example 1 25 ml of europium-activated yttrium oxysulfide (average particle size approximately 7 Buddhas) of red luminescent phosphor are suspended in 2500 ml of deionized water.
この蟹光体懸濁液の中に、10泌の塩化インジウム水溶
液(0.2裏rのln3十を毎必中に含む)を添加混合
する。ゆっくりと蝿拝しながら、塩酸のような酸を加え
てこの懸濁液のpHを約2.2(1〜3.6が許容範囲
)に調整する。次に、蝿拝しながら、硫化ナトリウムを
1.7釘含んだ水溶液約200のZを滴下して加える。
この混合液を礎拝しながら少なく共1時間熟成して、存
在するインジウムのほぼ全部を硫化インジウムの粒子と
して蟹光体粒子上に沈澱させる。次いで蟹光体表面に硫
化インジウム付着した固形物を沈降させ、上澄みを煩潟
し、沈降した固形物を脱イオン水で洗練し、固形物を約
125午0で乾燥する。乾燥した固形物250釘に硫黄
約7.5鱗を充分混合する。次にこの混合物を石英るつ
ぼに入れて、弱還元雰囲気で900℃30分間加熱する
。上記のようにして得た生成物の分光反射率を第1図に
示す。第1図は機軸に波長(nm)、縦軸に分光反射率
を示す。10 parts of an aqueous indium chloride solution (each containing 0.2 ln30) is added and mixed into this crab-photon suspension. While slowly stirring, adjust the pH of the suspension to about 2.2 (1-3.6 is acceptable) by adding an acid such as hydrochloric acid. Next, about 200 g of Z, an aqueous solution containing 1.7 g of sodium sulfide, is added dropwise while stirring.
This mixture is allowed to mature for at least one hour while being submerged, so that substantially all of the indium present is precipitated as indium sulfide particles on the crab phosphor particles. Next, the solid matter with indium sulfide attached to the surface of the crab light body is allowed to settle, the supernatant is filtered, the settled solid matter is purified with deionized water, and the solid matter is dried at about 125 minutes. Thoroughly mix about 7.5 scales of sulfur with 250 nails of dry solids. Next, this mixture is placed in a quartz crucible and heated at 900° C. for 30 minutes in a mildly reducing atmosphere. The spectral reflectance of the product obtained as described above is shown in FIG. In FIG. 1, the axis shows wavelength (nm) and the vertical axis shows spectral reflectance.
図中、線A−Aは本発明の硫化インジウムを被覆した赤
色発光蟹光体、線B−Bは従来のペンガラを被覆した赤
色発光蟹光体、線C−Cは顔料を被覆しない赤色発光蟹
光体を示す。この図かれも明らかなように本発明の硫化
インジウム被覆蟹光体は従来のペンガラ被覆蟹光体に比
べて60血の以上の長波長の反射率は高く、60血のよ
り短波長での反射率は低くコントラストが著しく向上す
ることがわかる。なお前記実施例では、硫化インジウム
を姿光体と共に沈澱させているが、硫化インジウムだけ
製造し、適当な結着材(例えば樟酸亜鉛等)で姿光体に
被着しても前記実施例と同様な分光反射率を有する顔料
被覆蟹光体を得ることができる。In the figure, line A-A is a red light-emitting crab light body coated with indium sulfide of the present invention, line B-B is a red light-emitting crab light body coated with conventional pengara, and line C-C is a red light-emitting light body that is not coated with pigment. Showing crab photophores. As is clear from this figure, the indium sulfide-coated crab light of the present invention has a higher reflectance at longer wavelengths of 60 or more than the conventional pengara-coated crab light, and has a higher reflectance at shorter wavelengths of 60 or more. It can be seen that the ratio is low and the contrast is significantly improved. In the above example, indium sulfide was precipitated together with the phosphor, but even if only indium sulfide was produced and coated on the phosphor with an appropriate binder (e.g. zinc acetate), the same could be said of the above example. It is possible to obtain a pigment-coated crab phosphor having a spectral reflectance similar to that of .
実施例 2塩化インジウム10雌rを脱イオン水250
凧【に溶解する。Example 2 Indium chloride 10 μl in deionized water 250 μl
Kite [dissolves in]
この水溶液中に硫化水素日ぶを毎分1そで3時間通して
水溶液中に存在するインジウムイオンの一部を硫化イン
ジウムの粒子として沈澱させる。次いで固形物を沈降さ
せ上澄を倭瀕して沈降した固形物を脱イオン水で洗総し
、固形物を約100℃で乾燥する。乾燥した固形物は赤
味がかった燈色を呈している。上記固形物100grに
硫黄3grを充分混合する。次にこの混合物を石英るつ
ぼに入れて弱還元性愛函気で500午○30分間焼成す
る。この焼成物は、0.5〜1#の粒径をもつ赤色硫化
インジウムの粒子よりなっている。次に約500ccの
水に上誌硫化インジウム粒子1grとユーロピウム付活
酸硫化イットリウム1008を懸濁させる。この懸濁液
をゆっくり麓拝しながら、水ガラスK20.$i02水
溶液(25モル%)1の‘を添加する。A portion of the indium ions present in the aqueous solution is precipitated as indium sulfide particles by passing hydrogen sulfide into this aqueous solution at a rate of 1 minute per minute for 3 hours. The solids are then allowed to settle, the supernatant is removed, the precipitated solids are washed with deionized water, and the solids are dried at about 100°C. The dried solid material has a reddish color. Thoroughly mix 3 gr of sulfur with 100 gr of the above solid material. Next, this mixture was placed in a quartz crucible and fired for 30 minutes at 500 pm using weakly reducing air. This fired product consists of red indium sulfide particles having a particle size of 0.5 to 1#. Next, 1g of the above indium sulfide particles and europium-activated yttrium oxysulfide 1008 are suspended in about 500cc of water. While slowly pouring over this suspension, water glass K20. Add 1 part of $i02 aqueous solution (25 mol%).
第1図は本発明蛍光体と従来の蛍光体の分光反射率を示
す図である。
第1図FIG. 1 is a diagram showing the spectral reflectance of the phosphor of the present invention and a conventional phosphor. Figure 1
Claims (1)
活酸硫化イツトリウム螢光体。1 Pigment coated europium activated yttrium oxysulfide phosphor coated with indium sulfide.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13988977A JPS603355B2 (en) | 1977-11-24 | 1977-11-24 | Pigment coated europium activated yttrium oxysulfide phosphor |
| US05/961,263 US4209567A (en) | 1977-11-24 | 1978-11-16 | Red pigment-coated phosphor and method of producing the same |
| GB7845316A GB2008608B (en) | 1977-11-24 | 1978-11-20 | Red pigment-coated phosphor and method of producing the same |
| DE2850491A DE2850491C2 (en) | 1977-11-24 | 1978-11-21 | Fluorescent screen substance and process for its manufacture |
| ES475382A ES475382A1 (en) | 1977-11-24 | 1978-11-24 | Red pigment-coated phosphor and method of producing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13988977A JPS603355B2 (en) | 1977-11-24 | 1977-11-24 | Pigment coated europium activated yttrium oxysulfide phosphor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5472782A JPS5472782A (en) | 1979-06-11 |
| JPS603355B2 true JPS603355B2 (en) | 1985-01-28 |
Family
ID=15255949
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13988977A Expired JPS603355B2 (en) | 1977-11-24 | 1977-11-24 | Pigment coated europium activated yttrium oxysulfide phosphor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS603355B2 (en) |
-
1977
- 1977-11-24 JP JP13988977A patent/JPS603355B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5472782A (en) | 1979-06-11 |
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