Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS6026067B2 - Transparent polycrystalline alumina composition and method for producing the same - Google Patents
[go: Go Back, main page]

JPS6026067B2 - Transparent polycrystalline alumina composition and method for producing the same - Google Patents

Transparent polycrystalline alumina composition and method for producing the same

Info

Publication number
JPS6026067B2
JPS6026067B2 JP56008724A JP872481A JPS6026067B2 JP S6026067 B2 JPS6026067 B2 JP S6026067B2 JP 56008724 A JP56008724 A JP 56008724A JP 872481 A JP872481 A JP 872481A JP S6026067 B2 JPS6026067 B2 JP S6026067B2
Authority
JP
Japan
Prior art keywords
weight
polycrystalline alumina
producing
alumina composition
same
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
Application number
JP56008724A
Other languages
Japanese (ja)
Other versions
JPS57123861A (en
Inventor
闊 瀬野
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.)
Murata Manufacturing Co Ltd
Original Assignee
Murata Manufacturing 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 Murata Manufacturing Co Ltd filed Critical Murata Manufacturing Co Ltd
Priority to JP56008724A priority Critical patent/JPS6026067B2/en
Publication of JPS57123861A publication Critical patent/JPS57123861A/en
Publication of JPS6026067B2 publication Critical patent/JPS6026067B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)

Description

【発明の詳細な説明】 本発明は機械的強度と高周波での電気的特性に秀れた透
光性多結晶アルミナ組成物およびその製造法に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a translucent polycrystalline alumina composition having excellent mechanical strength and electrical properties at high frequencies, and a method for producing the same.

一般に高純度多結晶アルミナは機械的、熱的強度、高周
波での電気的特性に秀れている他、透光性にも秀れてい
るため、多方面に有益な材料である。
In general, high-purity polycrystalline alumina has excellent mechanical and thermal strength, electrical properties at high frequencies, and excellent translucency, making it a useful material in many ways.

従来高純度多結晶アルミナはアルミナ微粉末に酸化マグ
ネシウム(Mg0)を徴量加えこれを所望の形に成形し
、予じめ空気中1000〜1300つ0で仮焼しバイン
ダーを充分に燃焼させて後、還元雰囲気中又は真空中で
1800〜1950午0、保温時間を1〜1餌時間とし
て焼成している。この従来の方法によれば透光性多結晶
アルミナはできるが、所望の品質を得るため焼成条件の
選定が極めて難しい。即ち、結晶粒子の異常成長を起こ
さずに凝結を充分に進めることが難しい。しかし、透光
性を良くするためには逆に粒子成長を充分にさせなけれ
ばならないが、このとき凝結体の機械的強度は著しく低
下して所望の品質を得ることが難しかった。本発明はこ
れらの点に鑑みてなされたもので、その要旨とするとこ
ろは酸化アルミニウム(山203)と、該酸化アルミニ
ウムに対し、0.07〜0.5重量%の酸化マグネシウ
ム(Mg0)および0.01〜0.箱重量%の二酸化マ
ンガン(MN02)からなる透光性多結晶アルミナ組成
物にある。
Conventionally, high-purity polycrystalline alumina is produced by adding a certain amount of magnesium oxide (Mg0) to fine alumina powder, molding it into the desired shape, and pre-calcining it in air at 1,000 to 1,300 degrees Celsius to fully burn the binder. After that, it is baked in a reducing atmosphere or in a vacuum from 1800 to 1950 pm, with a heat retention time of 1 to 1 feeding time. Although translucent polycrystalline alumina can be produced using this conventional method, it is extremely difficult to select firing conditions to obtain the desired quality. That is, it is difficult to sufficiently advance the coagulation without causing abnormal growth of crystal grains. However, in order to improve the translucency, it is necessary to allow sufficient particle growth, but at this time the mechanical strength of the aggregate decreases significantly, making it difficult to obtain the desired quality. The present invention was made in view of these points, and its gist is that aluminum oxide (mountain 203), 0.07 to 0.5% by weight of magnesium oxide (Mg0) and 0.01~0. The box consists of a translucent polycrystalline alumina composition consisting of % manganese dioxide (MN02) by weight.

本発明においてMg0と同時に添加するMn02はMg
0と同様に粒子の異常成長を抑え、強い抗折強度を保ち
ながら秀れた透光性を得る役目をはたす。
In the present invention, Mn02 added at the same time as Mg0 is Mg
Similar to 0, it suppresses the abnormal growth of particles and provides excellent translucency while maintaining strong bending strength.

この発明において組成範囲を限定した理由は次の通りで
ある。
The reason for limiting the composition range in this invention is as follows.

すなわち、Mg0が0.07以下、Mh02が0.01
以下の場合結晶粒子が異常成長し抗折強度が極めて弱く
なり、異常成長時、気孔を包含して透過率が低下する。
またMg0が0.5以上、Mn02が0.3以上では透
過率が低下するからである。前記組成物は次の方法によ
り製造するのが好ましい。
That is, Mg0 is 0.07 or less, Mh02 is 0.01
In the following cases, the crystal grains grow abnormally and the bending strength becomes extremely weak, and when the crystal grains grow abnormally, they include pores and the transmittance decreases.
Further, if Mg0 is 0.5 or more and Mn02 is 0.3 or more, the transmittance decreases. The composition is preferably manufactured by the following method.

すなわち、純度99.9%以上を有し粉末の平均粒子径
が0.08〜0.5r、比表面積が3〜10力/gのア
ルミナ粉末10の重量部に対し、第一の徴量添加物とし
て酸化マグネシウム(Mg○)または仮燐によりMやに
なるマグネシゥム化合物を0.07〜0.5重量部加え
、更に第二の徴量添加物として二酸化マンガン(Mn0
2)または仮銃によりMn02になるマンガン化合物を
0.01〜0.幻重量部加え、0.7〜1.5ton/
地の圧力で成形し、空気中1000〜1200午○で仮
暁後真空中(1〜5×10‐5肌Hg)又は水素雰囲気
中1780〜185ぴ○で焼成する製造方法である。な
お、焼成雰囲気を真空中又は水素雰囲気中としているの
は焼結過程において残留する気孔の除去を促進する役目
を果たすからである。
That is, the first amount is added to 10 parts by weight of alumina powder having a purity of 99.9% or more, an average particle diameter of 0.08 to 0.5r, and a specific surface area of 3 to 10 force/g. 0.07 to 0.5 parts by weight of magnesium oxide (Mg○) or a magnesium compound that becomes M due to temporary phosphorus are added as a substance, and manganese dioxide (Mn0) is added as a second component additive.
2) Or use a temporary gun to add a manganese compound that becomes Mn02 to 0.01 to 0. In addition to the phantom weight part, 0.7 to 1.5 tons/
This is a manufacturing method in which the product is molded under the same pressure as the ground, and after being cooled in air at 1,000 to 1,200 pm, it is fired in a vacuum (1 to 5 x 10-5 skin Hg) or in a hydrogen atmosphere at 1,780 to 185 pm. The reason why the firing atmosphere is a vacuum or a hydrogen atmosphere is because it serves to promote the removal of pores remaining during the sintering process.

以下、本発明についての実施例を説明する。Examples of the present invention will be described below.

実施例純度99.99%、粉末平均粒子径0.3ム、比
表面積5淋/gのアルミナ微粉末に純度99.5%以上
粉末平均粒子径0.5仏の酸化マグネシウムおよび二酸
化マンガンを表−1に示す如く添加し、原料と同じ量の
純水、酢酸ビニル8重量%を加え、直径15側の鋼球入
樹脂ボールを原料の1.5倍を用いて40時間湿式混合
し「 これを脱水乾燥して50メッシュの筋を通し、さ
らに同じ種類と量の樹脂ボールを用いて2時間乾式粉砕
後50メッシュの節を通して成形用造粒子とする。
Example Magnesium oxide and manganese dioxide with a purity of 99.5% or more and a powder average particle size of 0.5 μm are added to fine alumina powder with a purity of 99.99%, a powder average particle size of 0.3 μm, and a specific surface area of 5 mm/g. Add the same amount of pure water as the raw material and 8% by weight of vinyl acetate, and wet-mix for 40 hours using a resin ball with a diameter of 15 steel balls at 1.5 times the raw material. The powder is dehydrated and dried, passed through a 50-mesh thread, and then dry-pulverized for 2 hours using the same type and amount of resin balls, and then passed through a 50-mesh knot to form particles for molding.

次に直径30帆、厚み1.3柵の円板と、直径5.3肋
、厚さ3仇舷の円柱にlton/塊の圧力で成形する。
Next, it is molded into a disk with a diameter of 30 sails and a thickness of 1.3 fences, and a cylinder with a diameter of 5.3 ribs and a thickness of 3 yards using a pressure of lton/lump.

これを空気中50〜7び○/hrで昇溢ごせ1100q
oで2時間保持後、自然冷却させる。この仮焼物を真空
中(1〜5×10‐5肋Hg)100℃/hrで昇温し
、1810『0で2時間保持後250qo/hrで冷却
して測定用試料とした。この試料の結晶粒子径は円板を
金属顕微鏡を用いて50ケのグリーン径の平均値、抗折
強度は円柱を用いてJIS規格に基づいて支点間距離は
2物舷としての試料数10ケの平均値、透過率の測定は
、円板の両面をG.C.#800で研磨後、赤外分光光
度計を用いて波長1.5〜15山の領域での拡散透過率
の最高値で用いた。結果を表−1に示す。表一2には従
来例を示す。表一1中M.1〜15は本発明の実施例を
、No.16〜19は本発明の範囲外の参考例をそれぞ
れ示す。表−1 表−2 表−2には従来例を示してあるが、この組成物で秀れた
透過率を得るためには結晶粒子径を大き〈する必要があ
るが、この時抗折強度が極めて弱くなることがわかる。
Rinse this in the air at 50~7 ○/hr for 1100q.
After holding at o for 2 hours, let it cool naturally. This calcined product was heated in vacuum (1 to 5 x 10-5 Hg) at a rate of 100°C/hr, held at 1810°C for 2 hours, and then cooled at 250 qo/hr to obtain a measurement sample. The crystal grain size of this sample was measured using a metallurgical microscope using a disk, and the average value of 50 Green's diameters was measured, and the bending strength was measured based on the JIS standard using a cylinder. To measure the average value and transmittance of G. C. After polishing with #800, an infrared spectrophotometer was used at the highest value of diffuse transmittance in the wavelength range of 1.5 to 15 peaks. The results are shown in Table-1. Table 1-2 shows a conventional example. M. in Table 11. No. 1 to 15 are examples of the present invention. Reference examples 16 to 19 are outside the scope of the present invention. Table 1 Table 2 Table 2 shows a conventional example. In order to obtain excellent transmittance with this composition, it is necessary to increase the crystal particle size, but in this case, the bending strength It can be seen that it becomes extremely weak.

本発明はこの点を改良したもので、AI203−Mg○
系にMh02を添加することによって透れた秀逸率を得
て、かつ結晶粒子径を小さくして強い抗折強度が得られ
るという効果を奏し、また本発明の組成物はアルミナ含
有率が高く、かつ暁結体が極めて繊密なため高周波、特
にG世帯での誘電体損失が極めて小さく、誘電体材料と
しても有益0である。代表的3例についての測定結果を
表−1右欄に示す。本発明においての添加物は酸化物粉
末のかわりに塩化物、炭酸塩としても同様の結果が得ら
れる。以上の様に本発明によれば、機械的及び電気的タ
特性に秀れた透過性結晶アルミナが得られる。
The present invention improves this point, and AI203-Mg○
By adding Mh02 to the system, it is possible to obtain an excellent transparency rate and to reduce the crystal grain size to obtain strong bending strength, and the composition of the present invention has a high alumina content, In addition, since the Akatsuki crystal is extremely dense, the dielectric loss at high frequencies, especially in the G household, is extremely small, making it useful as a dielectric material. The measurement results for three representative examples are shown in the right column of Table 1. Similar results can be obtained by using chloride or carbonate instead of oxide powder as the additive in the present invention. As described above, according to the present invention, transparent crystalline alumina having excellent mechanical and electrical properties can be obtained.

Claims (1)

【特許請求の範囲】 1 酸化アルミニウム(Al_2O_3)と、該酸化ア
ルミニウムに対し、0.07〜0.5重量%の酸化マグ
ネシウム(MgO)および0.01〜0.3重量%の二
酸化マンガン(MnO_2)からなる透光性多結晶アル
ミナ組成物。 2 純度99.9%以上を有し、粉末の平均粒子径が0
.08〜0.5μ、比表面積が3〜10m^2/gのア
ルミナ粉末100重量部に対し、酸化マグネシウムまた
は酸化マグネシウム形成化合物を0.07〜0.5重量
部と、二酸化マンガンまたは二酸化マンガン形成化合物
を0.01〜0.3重量部加えて成形し、空気中100
0〜1200℃で仮焼した後、真空中または水素零囲気
中1780〜1850℃で焼成すること特徴とする透光
性多結晶アルミナ組成物の製造方法。
[Claims] 1 Aluminum oxide (Al_2O_3), 0.07 to 0.5% by weight of magnesium oxide (MgO) and 0.01 to 0.3% by weight of manganese dioxide (MnO_2 ) A translucent polycrystalline alumina composition. 2 The purity is 99.9% or more, and the average particle size of the powder is 0.
.. Manganese dioxide or manganese dioxide formation by adding 0.07 to 0.5 parts by weight of magnesium oxide or a magnesium oxide forming compound to 100 parts by weight of alumina powder with a specific surface area of 08 to 0.5μ and a specific surface area of 3 to 10 m^2/g. Add 0.01 to 0.3 parts by weight of the compound and mold, and
A method for producing a translucent polycrystalline alumina composition, which comprises calcining at 0 to 1200°C and then firing at 1780 to 1850°C in vacuum or in a hydrogen atmosphere.
JP56008724A 1981-01-22 1981-01-22 Transparent polycrystalline alumina composition and method for producing the same Expired JPS6026067B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56008724A JPS6026067B2 (en) 1981-01-22 1981-01-22 Transparent polycrystalline alumina composition and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56008724A JPS6026067B2 (en) 1981-01-22 1981-01-22 Transparent polycrystalline alumina composition and method for producing the same

Publications (2)

Publication Number Publication Date
JPS57123861A JPS57123861A (en) 1982-08-02
JPS6026067B2 true JPS6026067B2 (en) 1985-06-21

Family

ID=11700893

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56008724A Expired JPS6026067B2 (en) 1981-01-22 1981-01-22 Transparent polycrystalline alumina composition and method for producing the same

Country Status (1)

Country Link
JP (1) JPS6026067B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6083451A (en) * 1995-04-18 2000-07-04 Applied Materials, Inc. Method of producing a polycrystalline alumina ceramic which is resistant to a fluorine-comprising plasma
JP4729705B2 (en) * 2006-01-06 2011-07-20 国立大学法人鳥取大学 Method for producing translucent alumina sintered body and method for producing optical filter

Also Published As

Publication number Publication date
JPS57123861A (en) 1982-08-02

Similar Documents

Publication Publication Date Title
US4273587A (en) Polycrystalline transparent spinel sintered body and a method for producing the same
JP2000219570A (en) Method for producing translucent alumina sintered body and use thereof
JPS6140621B2 (en)
JP3420377B2 (en) Method for producing yttrium-aluminum-garnet sintered body
KR20230147153A (en) Dense green tape, its manufacturing method and uses
JP3285620B2 (en) Method for producing translucent yttrium-aluminum-garnet sintered body
JPS6026067B2 (en) Transparent polycrystalline alumina composition and method for producing the same
JPS6045147B2 (en) Transparent polycrystalline alumina composition and method for producing the same
JPS6026068B2 (en) Transparent polycrystalline alumina composition and method for producing the same
JP2558849B2 (en) Method for producing transparent aluminum oxynitride composite sintered body
WO2013051576A1 (en) Conductive mayenite compound sintered compact, sputtering target, and method for producing conductive mayenite compound sintered compact
US3421914A (en) Process for making porous light-weight zirconia bodies
JPS6031795B2 (en) Zirconia sintered body
JP3245234B2 (en) Method for producing translucent yttrium-aluminum-garnet sintered body
JPS647030B2 (en)
JP2006256934A (en) High dielectric material and manufacturing method thereof
JP2510705B2 (en) Method for producing transparent aluminum oxynitride composite sintered body
KR20250025697A (en) Manufacturing process of monolithic compacted alumina material for single crystal growth
JPS61181008A (en) Manufacture of dielectric ceramics
JPH0234516A (en) Production of tl-ba-ca-cu-o type superconducting ceramics
JPH0335260B2 (en)
JPS6319447B2 (en)
JPS6158431B2 (en)
JPH01252529A (en) Production of tl-ca-sr-cu-o superconducting oxide powder
JPH02116664A (en) Preparation of sintered body of mullite