JPS60139784A - Phosphor - Google Patents

Phosphor

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Publication number
JPS60139784A
JPS60139784A JP25070483A JP25070483A JPS60139784A JP S60139784 A JPS60139784 A JP S60139784A JP 25070483 A JP25070483 A JP 25070483A JP 25070483 A JP25070483 A JP 25070483A JP S60139784 A JPS60139784 A JP S60139784A
Authority
JP
Japan
Prior art keywords
phosphor
oxide
europium
yttrium oxide
peak height
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
JP25070483A
Other languages
Japanese (ja)
Other versions
JPH0629416B2 (en
Inventor
Katsuaki Iwama
克昭 岩間
Takashi Yamamoto
山本 高詩
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electronics Corp
Matsushita Electric Industrial Co Ltd
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 Matsushita Electronics Corp, Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electronics Corp
Priority to JP58250704A priority Critical patent/JPH0629416B2/en
Publication of JPS60139784A publication Critical patent/JPS60139784A/en
Publication of JPH0629416B2 publication Critical patent/JPH0629416B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Luminescent Compositions (AREA)

Abstract

PURPOSE:To improve the peak height of luminescence, by dissolving yttrium oxide in a bivalent europium-activated barium aluminate phosphor. CONSTITUTION:Starting materials such as yttrium oxide, barium oxide, aluminum oxide and europium oxide or nitrates or halides of these elements are weighed. A small quantity of boric acid, etc. is added thereto and the mixture is crushed and mixed with one another in a ball mill, packed in a quartz boat and calcined at 1,100-1,600 deg.C in a reducing atmosphere for several hour to obtain the desired phosphor. The peak height of luminescence of the resulting phosphor generated by ultraviolet light excitation is 105-110% of that of conventional europium-activated barium aluminate phosphor contg. no yttrium oxide.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は2価のユーロピウムで付活されたバリウムアル
ミネート螢光体の改良に関するものである0 従来例の構成゛とその問題点 従来、2価のユーロピウムで付活されたツリウムアルミ
ネート螢光体としては、、C5BLASSICandム
、 BRIL 、 philips Res 、 Re
pt−t 23 (196B)201 に研究報告があ
り、B&ム1,04: Ru2X−よびBaム1120
□HRu の発光ピーク波長はそれぞれs o a n
uおよび435nlllであることが知られている。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to improvements in barium aluminate phosphors activated with divalent europium. Europium-activated thulium aluminate phosphors include C5BLASSICandum, BRIL, philips Res, Re
There is a research report in pt-t 23 (196B) 201, B & M 1,04: Ru2X- and Bam 1120
□The emission peak wavelength of HRu is
u and 435nllll.

近年、高演色性螢光ランプの効率改善に関して、480
〜soonmに発光ピークを有する螢光体が注口されて
いる。最近の研究によれば、例えば、J、T、(3,V
AN KICMINADK and G、P、F。
In recent years, 480 papers have been published regarding efficiency improvement of high color rendering fluorescent lamps.
A phosphor having an emission peak at ~soonm is poured. According to recent research, for example, J, T, (3, V
AN KICMINADK and G, P, F.

HOEKS、Extended ab 5tract 
No、607゜K、(3,S、Spring Meet
ing(19ss)に報告されているBaム111O,
3: Eu2+螢光体は発光ピーク波長が480nmに
ある新しいタイプのアルミネートである′0しかしなが
ら、この2価のユーロピウムで付活され産前緑色螢光体
は発光ピーク高さが不十分であり、その向上が望まれて
いた〇発明の目的 本発明は、このような事情にもとづいてなされたもので
、発光ピーク高さを向上させた2価のユーロピウム付活
アルミネート螢光体全提供することをローとするもので
ある。
HOEKS, Extended ab 5tract
No, 607°K, (3, S, Spring Meet
Bam 111O reported in ing (19ss),
3: Eu2+ phosphor is a new type of aluminate with an emission peak wavelength of 480 nm. However, the prenatal green phosphor activated with divalent europium has an insufficient emission peak height; It was desired to improve the above.Objective of the Invention The present invention was made based on the above circumstances, and an object of the present invention is to provide a divalent europium-activated aluminate phosphor with improved emission peak height. is low.

発明の構成 発明者らは、2価のユーロピウムで付活されたバリウム
アルミネート螢光体について詳細な実験を行なった結果
、この螢光体にさらに酸化イットリウムを固溶させるこ
とによって、その発光ピーク高さ全一層内上させ得るこ
とを見出した。
Components of the Invention The inventors conducted detailed experiments on a barium aluminate phosphor activated with divalent europium, and found that by dissolving yttrium oxide in this phosphor, the emission peak of the phosphor could be improved. It has been found that the height can be increased by one layer.

すなわち、発明者らの実験によれば、2価のユーロピウ
ムで付活さ、れたバリウムアルミネート螢光体は、その
組成式が (Ba、Eu)Orxム1203ay¥203で表わさ
れるものであり、上記組成式のx、yの範囲がそれぞれ 3くxく5.0〈yく0.1 の場合に、より−好ましい発光ピーク高さの向上が認め
られたものである。さらに言えば、本発、明に、かかる
螢光体の場合、そのAl2O3量X・が3〉xまたは5
〈xの領域においても、酸化イツトリウムの固溶により
発光ピーク高さが向上するという効果は明らかに認めら
れたが、これらの向上されたピーク高さをもってしても
現在実用されているBaA180,3: Ru 螢光体
の発光ピーク高さを越えるものは得られず、実用的なレ
ベルには至らないことを確認した。また、付活剤である
ユーロピウム添加量は、他の一般に使用されている螢光
体におけるユーロピウム濃度の範囲で上記酸化イツトリ
ウム固溶による発光ピーク高さの向上効果が認められた
That is, according to the inventors' experiments, the barium aluminate phosphor activated with divalent europium has a compositional formula of (Ba, Eu) Orxum 1203ay ¥203. A more preferable improvement in the height of the emission peak was observed when the ranges of x and y in the above compositional formula were 3 x 5.0 < y x 0.1, respectively. Furthermore, the present invention specifies that in the case of such a phosphor, the amount of Al2O3 is 3>x or 5
〈Even in the region of : It was confirmed that the emission peak height exceeding that of the Ru phosphor could not be obtained, and that it did not reach a practical level. Further, regarding the amount of europium added as an activator, the effect of improving the luminescence peak height due to the solid solution of yttrium oxide was observed within the range of europium concentrations found in other commonly used phosphors.

実施例の説明 −本発明にかかる螢光体は以下に述べる製造方法によっ
て得られる。まず、螢光体原料としては、(1)酸化イ
ツトリウム(Y2O3,)またば硝酸塩・炭酸塩、ハロ
ゲン化物等の高温で容易にY2O,K変化し得る化合物
Description of Examples - The phosphor according to the present invention is obtained by the manufacturing method described below. First, as raw materials for the phosphor, (1) yttrium oxide (Y2O3,) or compounds that can be easily converted to Y2O and K at high temperatures, such as nitrates, carbonates, and halides;

(2)酸化バリウムCB&0)または硝酸塩、炭酸塩ハ
ロゲン化物等の高温で容易にBaOに変化し得る化合物
(2) Compounds that can be easily converted to BaO at high temperatures, such as barium oxide CB&0) or nitrates, carbonates, and halides.

(3)酸化アルミニウム(ム1203) ’jたけ硝酸
塩。
(3) Aluminum oxide (Mu1203)'jtake nitrate.

水酸化物、ノ・ロゲン化物等の高温で容易にAl、0.
に変化し得る化合物。
Al, 0.
A compound that can change into

(4) 酸化ユーロピウム(lCu2O,)または硝酸
塩。
(4) Europium oxide (lCu2O,) or nitrate.

炭酸塩、ハロゲン化物等の高温で容易にEu2O3に変
化し得る化合物。
Compounds that can be easily converted to Eu2O3 at high temperatures, such as carbonates and halides.

が用いられる。上記原料を秤量し、ホウ酸、無水ホウ酸
などを適量添加して、ボールミルにより十分に粉砕混合
する0これを石英ポートに充填し、還元雰囲気中におい
て1100〜1600℃の範囲内の温度で数時間焼成す
ることによって螢光体を得る。
is used. Weigh the above raw materials, add an appropriate amount of boric acid, boric anhydride, etc., and thoroughly pulverize and mix using a ball mill.Fill this into a quartz port and heat several times at a temperature within the range of 1100 to 1600°C in a reducing atmosphere. A phosphor is obtained by baking for a period of time.

以下、本発明の実施例について述べる。Examples of the present invention will be described below.

実施例1 、 酸化イツトリウム Q、11 g 炭酸バリウム 1.8.74 酸化アルミニウム 4.0.80 酸化ユーロピウム 0.88 無水ホウ酸 0.70 上記原料をボールミルにて十分に粉砕混合し、還元性雰
囲気中、1100〜1600°Cの温度で数時間焼成し
、螢光体を得た0 得られた螢光体の組成式は次のとおりである。
Example 1 Yttrium oxide Q, 11 g Barium carbonate 1.8.74 Aluminum oxide 4.0.80 Europium oxide 0.88 Boric anhydride 0.70 The above raw materials were sufficiently pulverized and mixed in a ball mill and mixed in a reducing atmosphere. A phosphor was obtained by firing at a temperature of 1,100 to 1,600° C. for several hours.The compositional formula of the obtained phosphor is as follows.

(Hao、1. K’uo、o、 ) 064 Al、
0.@ o、oosy2o。
(Hao, 1. K'uo, o, ) 064 Al,
0. @ o, oosy2o.

この螢光体の紫外線励起による発光ピーク高さは酸化イ
・トリク・を含ま茫い従来の螢光体(B ao、 、5
 Ruo、65 ) os 4ム1203の発光ピーク
高さに比べて110チであり、明らかな向上が認められ
た0 実施例2 フッ化イツトリウム 0・73g 炭酸バリウム 17.76 酸化アルミニウム 51.00 酸化ユーロピウム 1.76 ホウ酸 2−68 上記原料を用い、実施例1と同様にして螢光体を得た。
The height of the emission peak of this phosphor upon excitation with ultraviolet rays is higher than that of conventional phosphors (Bao, 5
Ruo, 65) Compared to the emission peak height of os 4 1203, it was 110 cm, a clear improvement was observed0 Example 2 Yttrium fluoride 0.73 g Barium carbonate 17.76 Aluminum oxide 51.00 Europium oxide 1.76 Boric acid 2-68 A phosphor was obtained in the same manner as in Example 1 using the above raw materials.

得られた螢光体の組成式は次のとおりである。The compositional formula of the obtained phosphor is as follows.

(Bao、o ICuo4 ) Om 5ム1203−
0.0025Y20゜この螢光体の紫外線励起による発
光ピーク高さは、酸化イツ) IJウムを含まない従来
の螢光体(Bao、、; Euo、、 ) O−6ム1
203の発光ピーク高さに比べて106%であり、明ら
かな向上が認められた0□ □ 実施例3 フッ化イツトリウム 2・91g 炭酸バリウム 19.34 酸化アルミニウム 35.70 酸化ユーロピウム 0・36 ホウ酸 1.34 上記原料を用い、実施例1と同様にして螢光体を得た。
(Bao, o ICuo4) Om 5mu 1203-
0.0025Y20゜The height of the emission peak of this phosphor upon excitation with ultraviolet rays is 0.0025Y20°.
This was 106% compared to the emission peak height of 203, and a clear improvement was observed.0 □ □ Example 3 Yttrium fluoride 2.91 g Barium carbonate 19.34 Aluminum oxide 35.70 Europium oxide 0.36 Boric acid 1.34 A phosphor was obtained in the same manner as in Example 1 using the above raw materials.

得られた螢光体の組成式は次のとお9である。The compositional formula of the obtained phosphor is 9 below.

(Bao、、81Cuo、o2) O@3.5 A12
4)、 ++0.1Y20゜この螢光体の紫外線励起に
よる発光ピーク高さは酸化イツトリウムを含まない従来
の螢光体0”0.9 s ”uo、o 2 ) 0 ・
3. tsム1203の発光ピーク高さに比べて107
%であり、明らかな向上が認められた。
(Bao,,81Cuo,o2) O@3.5 A12
4), ++0.1Y20° The height of the emission peak of this phosphor due to ultraviolet excitation is 0"0.9 s"uo, o 2 ) 0 ・
3. 107 compared to the emission peak height of TSM 1203.
%, a clear improvement was observed.

上記各実施例において、フラックスとして用いているホ
ウ素含有化合物は得られた螢光体中に、例えば(Ba、
 Eu)O@4ム120.に対して0.05B2011
量が残っていることが認められたが、本螢光体の結晶構
造に大きく影響するものではなく、また発光特性に対し
ても、とくに悪い影響はなく、必要であれば・水洗等の
後処理によりある程度は除去することができるものであ
る。
In each of the above Examples, the boron-containing compound used as a flux was contained in the obtained phosphor, for example (Ba,
Eu)O@4mu120. 0.05B for 2011
Although it was observed that some amount remained, it did not significantly affect the crystal structure of the phosphor, nor did it have any particular negative effect on the luminescent properties. It can be removed to some extent through treatment.

発明の詳細 な説明したように、本発明は2価のユーロピウム付活バ
リウム・アルミネート螢光体に酸化イツトリウムを固溶
させることによって、発光ピーク高さを向上させた優れ
た螢光体を提供することができるものである。
As described in detail, the present invention provides an excellent phosphor with improved emission peak height by dissolving yttrium oxide in a divalent europium-activated barium aluminate phosphor. It is something that can be done.

Claims (1)

【特許請求の範囲】[Claims] 2価のユーロピウムで付活されたバリウムアルミネート
螢光体に酸化イツトリウムを固溶させてなることを特徴
とする螢光体。
A phosphor comprising a barium aluminate phosphor activated with divalent europium and a solid solution of yttrium oxide.
JP58250704A 1983-12-27 1983-12-27 Fluorescent body Expired - Lifetime JPH0629416B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58250704A JPH0629416B2 (en) 1983-12-27 1983-12-27 Fluorescent body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58250704A JPH0629416B2 (en) 1983-12-27 1983-12-27 Fluorescent body

Publications (2)

Publication Number Publication Date
JPS60139784A true JPS60139784A (en) 1985-07-24
JPH0629416B2 JPH0629416B2 (en) 1994-04-20

Family

ID=17211798

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58250704A Expired - Lifetime JPH0629416B2 (en) 1983-12-27 1983-12-27 Fluorescent body

Country Status (1)

Country Link
JP (1) JPH0629416B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100381618C (en) * 2006-08-30 2008-04-16 大连理工大学 Method for preparing aluminate long-persistence luminous plate

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6267911B1 (en) 1997-11-07 2001-07-31 University Of Georgia Research Foundation, Inc. Phosphors with long-persistent green phosphorescence

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5876486A (en) * 1981-10-30 1983-05-09 Matsushita Electronics Corp Fluorescent material

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5876486A (en) * 1981-10-30 1983-05-09 Matsushita Electronics Corp Fluorescent material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100381618C (en) * 2006-08-30 2008-04-16 大连理工大学 Method for preparing aluminate long-persistence luminous plate

Also Published As

Publication number Publication date
JPH0629416B2 (en) 1994-04-20

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