JPS5933535B2 - Compound having hexagonal layered structure represented by YbGaMnO↓4 and method for producing the same - Google Patents

Compound having hexagonal layered structure represented by YbGaMnO↓4 and method for producing the same

Info

Publication number
JPS5933535B2
JPS5933535B2 JP6503881A JP6503881A JPS5933535B2 JP S5933535 B2 JPS5933535 B2 JP S5933535B2 JP 6503881 A JP6503881 A JP 6503881A JP 6503881 A JP6503881 A JP 6503881A JP S5933535 B2 JPS5933535 B2 JP S5933535B2
Authority
JP
Japan
Prior art keywords
compound
layered structure
ybgamno
structure represented
hexagonal layered
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
JP6503881A
Other languages
Japanese (ja)
Other versions
JPS57179024A (en
Inventor
昇 君塚
英治 高山
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.)
KAGAKU GIJUTSUCHO MUKIZAISHITSU KENKYUSHOCHO
Original Assignee
KAGAKU GIJUTSUCHO MUKIZAISHITSU KENKYUSHOCHO
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 KAGAKU GIJUTSUCHO MUKIZAISHITSU KENKYUSHOCHO filed Critical KAGAKU GIJUTSUCHO MUKIZAISHITSU KENKYUSHOCHO
Priority to JP6503881A priority Critical patent/JPS5933535B2/en
Publication of JPS57179024A publication Critical patent/JPS57179024A/en
Publication of JPS5933535B2 publication Critical patent/JPS5933535B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は新規化合物であるYbGaMnO4で示される
六方晶系の層状構造を有する化合物およびその製造法に
関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel compound YbGaMnO4 having a hexagonal layered structure and a method for producing the same.

従来、YFe204で示される六方晶系の層状構造を有
する化合物は知られる。
Conventionally, a compound having a hexagonal layered structure represented by YFe204 is known.

この化合物はY3+Fe2+Fe3+01〜で示される
ように、鉄の2価イオンと3価イオンは5配位の酸素イ
オンに囲まれ、Yは6配位の酸素イオンをその周りに持
つている化合物であり、磁性を持つている。本発明は前
記Y3+Fe2+Fe3+01−化合物のY3+の代わ
りにYb3+、Fe2+の代わりにMn2+を、Fe3
+の代わりにGa3+を置きかえた新規な化合物および
その製造法を提供するにある。本発明のYbGaMnO
4で示される化合物は、この化合物中、イッテルビウム
はYb3+イオン、マンガンはMn2+、ガリウムは3
価イオンとして存在しており、Yb3+Ga3+Mn2
+01−として表わすことができる。
This compound is a compound in which divalent and trivalent iron ions are surrounded by five-coordinated oxygen ions, and Y has six-coordinated oxygen ions around it, as shown by Y3+Fe2+Fe3+01~. It has magnetism. The present invention uses Yb3+ in place of Y3+ in the Y3+Fe2+Fe3+01- compound, Mn2+ in place of Fe2+, Fe3
The object of the present invention is to provide a novel compound in which + is replaced with Ga3+, and a method for producing the same. YbGaMnO of the present invention
In the compound represented by 4, ytterbium is a Yb3+ ion, manganese is a Mn2+ ion, and gallium is a 3+ ion.
Exists as valence ions, Yb3+Ga3+Mn2
It can be expressed as +01-.

この結晶は第1図に示すような六方晶層状構造を持つて
いる。最大の丸は酸素、中丸はYb、最小の黒丸はGa
とMnを示す。
This crystal has a hexagonal layered structure as shown in FIG. The largest circle is oxygen, the middle circle is Yb, and the smallest black circle is Ga.
and Mn.

GaとMnはランダムに入つている。マンガンの2価イ
オンとGaの3価イオンは5配位の酸素イオンによつて
囲まれ、結晶学的には同一の位置を占めている。またY
bは6配位の酸素をその周りに持つている。陰イオンで
ある酸素は緻密構造をとつている。s、をおよびuは単
位格子内における位置を示す。この結晶の両指数(hk
l)、面間隔(dλ)(doは実測、dcは計算値を示
す)、X線に対する相対反射強度(I%)は第1表の通
りである。
Ga and Mn are entered randomly. The divalent ions of manganese and the trivalent ions of Ga are surrounded by five-coordinated oxygen ions and occupy the same position crystallographically. Also Y
b has six-coordinated oxygen around it. Oxygen, an anion, has a dense structure. s, and u indicate the position within the unit cell. Both indices of this crystal (hk
Table 1 shows the relative reflection intensity (I%) for X-rays.

そして空間群はR3mで、その晶癖は板状晶で、格子定
数は次の通りである。ao■ 3.4437±O、0O
02(λ)c0=25.709±O、003(Λ)第1
表YbGaMn04 この化合物は触媒材料ならびに半導体材料として有用な
ものである。
The space group is R3m, the crystal habit is plate-like, and the lattice constant is as follows. ao ■ 3.4437±O, 0O
02 (λ) c0 = 25.709 ± O, 003 (Λ) 1st
Table YbGaMn04 This compound is useful as a catalyst material as well as a semiconductor material.

この化合物は次の方法によつて製造し得られる。This compound can be produced by the following method.

イツテルビウム酸化物(Yb2O3)、マンガン酸化物
(MnO)および酸化ガリウム(Ga2O3)を、モル
比で約1対2対1の割合で混合し、該混合物を非酸化性
雰囲気下で700℃以上の温度で加熱することによつて
製造することができる。本発明に用いるイッテルビウム
酸化物は市販のものをそのまま使用してもよいが、酸化
物相互の反応を速やかに進行させるためには、粒径が小
さい程よく、特に10μm以下であることが好ましい。
また半導体材料として用いる場合は不純物の混入をきら
うので、原料は純度が高く、また、約1000℃で数時
間空気中で仮焼したものが望ましい。酸化マンガンは通
常の試薬特毀程度のものでよい。
Ytterbium oxide (Yb2O3), manganese oxide (MnO) and gallium oxide (Ga2O3) are mixed in a molar ratio of approximately 1:2:1, and the mixture is heated at 700°C or higher in a non-oxidizing atmosphere. It can be produced by heating at a certain temperature. Commercially available ytterbium oxides used in the present invention may be used as they are, but in order to speed up the reaction between the oxides, the smaller the particle size, the better, particularly preferably 10 μm or less.
When used as a semiconductor material, since contamination with impurities is to be avoided, the raw material should preferably be of high purity and should have been calcined in air at about 1000° C. for several hours. Manganese oxide can be used as a normal reagent.

粒径は前記イッテルビウム酸化物と同様な理由で10μ
m以下であることが好ましい。また、1000℃で1日
間炭酸ガスと水素の混合ガス(混合比容量で1対1)中
で仮焼し、O℃に急冷させたものが反応が早くなるので
好ましい。酸化ガリウムは試薬特級程度のものでよい。
その粒径は前記と同様に10ttm以下であることが好
ましい。また800℃で1日間空気中で仮焼したものが
好ましい。これらの原料をそのまま、あるいはアルコー
ル類、アセトン等を入れ十分混合する。これらの混合割
合はYb2O3、MnO.Ga2O3をモル比で1対2
対1の割合である。この割合をはずれると目的とする層
状化合物を得ることができない。これらの混合物を石英
またはガラスの容器に封入して非酸化性雰囲気下で加熱
する。
The particle size is 10μ for the same reason as the ytterbium oxide.
It is preferable that it is below m. Further, it is preferable to calcinate in a mixed gas of carbon dioxide and hydrogen (mixture ratio: 1:1 by volume) at 1000° C. for 1 day, and then rapidly cool to 0° C., because the reaction speeds up. The gallium oxide may be of special reagent grade.
The particle size is preferably 10 ttm or less as described above. Moreover, it is preferable to calcined in air at 800° C. for one day. These raw materials are thoroughly mixed as they are or with alcohol, acetone, etc. added. These mixing ratios are Yb2O3, MnO. Ga2O3 molar ratio 1:2
The ratio is 1:1. If this ratio is exceeded, the desired layered compound cannot be obtained. These mixtures are sealed in a quartz or glass container and heated under a non-oxidizing atmosphere.

それはマンガンが2価の状態であるので、酸化性雰囲気
(例えば大気中)下ではマンガンが酸化させて3価にな
つてしまうので、非酸化性雰囲気下であることが必要で
ある。加熱温度は700℃以上であればよく、また加熱
時間は10分以上、好ましくは1時間以上である。加熱
の際の昇温速度は制やはない。反応終了後はO℃に急冷
するかあるいは大気中に急激に引出せばよい。得られた
YbGaMnO4化合物は黒色を有し、粉末X線回折法
によつて結晶構造を有することが分つた。
Since manganese is in a divalent state, in an oxidizing atmosphere (for example, in the atmosphere), manganese will oxidize and become trivalent, so it is necessary to be in a non-oxidizing atmosphere. The heating temperature may be 700° C. or more, and the heating time is 10 minutes or more, preferably 1 hour or more. There is no limit to the rate of temperature increase during heating. After the reaction is completed, it may be rapidly cooled to 0°C or rapidly drawn out into the atmosphere. The obtained YbGaMnO4 compound had a black color and was found to have a crystalline structure by powder X-ray diffraction.

試料の重量を加熱の前後に於いて精密に秤量し、実1験
誤差の範囲内で変化がないことが確認され、化学量論数
が決定された。実施例 純度99.9%以上のイツテルビウム酸化物(Yb2O
3)粉末、純度99.9%以上の酸化マンガン(MnO
)粉末および純度99,9%以上のガリウム酸化物(G
a2O3)粉末をモル比で1対2対1の割合に秤量し、
乳鉢でアセトンを加えて十分に混合して平均粒径数μm
の微粉末混合物を得た。
The weight of the sample was precisely weighed before and after heating, and it was confirmed that there was no change within the experimental error range, and the stoichiometric number was determined. Examples Ytterbium oxide (Yb2O) with a purity of 99.9% or more
3) Powder, manganese oxide (MnO) with a purity of 99.9% or more
) powder and gallium oxide (G
a2O3) powder in a molar ratio of 1:2:1,
Add acetone in a mortar and mix thoroughly until the average particle size is several μm.
A fine powder mixture was obtained.

該混合物を透明石英管(内径8mTIL)内に入れて真
空ポンプを用いて管内を10−3m1LHgq眞空度に
下げ、約1時間維持し、ガスバーナーで溶封した。これ
を1000℃に設定された箱型のシリコニツト炉内に入
れ、約5日間加熱し、その後試料を取出し、室温まで急
速に冷却した。得られたものはYbGaMnO4の六方
晶系の層状化合物であつた。その結晶の性状は第1表に
示す通りであつた。
The mixture was placed in a transparent quartz tube (inner diameter 8 m TIL), and the inside of the tube was lowered to 10 −3 mL Hgq vacuum using a vacuum pump, maintained for about 1 hour, and then sealed using a gas burner. This was placed in a box-shaped siliconite furnace set at 1000°C and heated for about 5 days, after which the sample was taken out and rapidly cooled to room temperature. What was obtained was a hexagonal layered compound of YbGaMnO4. The properties of the crystal were as shown in Table 1.

【図面の簡単な説明】[Brief explanation of the drawing]

図面は本発明のYbGaMnO4の結晶の図である。 The drawing is a diagram of the YbGaMnO4 crystal of the present invention.

Claims (1)

【特許請求の範囲】 1 YbGaMnO_4で示される六方晶系の層状構造
を有する化合物。 2 イッテルビウム酸化物(Yb_2O_3)、マンガ
ン酸化物(MnO)およびガリウム酸化物(Ga_2O
_3)を、モル比で約1対2対1の割合で混合し、この
混合物を非酸化性雰囲気下700℃以上の温度で加熱す
ることを特徴とするYbGaMnO_4で示される六方
晶系の層状構造を有する化合物の製造法。
[Scope of Claims] 1 A compound having a hexagonal layered structure represented by YbGaMnO_4. 2 Ytterbium oxide (Yb_2O_3), manganese oxide (MnO) and gallium oxide (Ga_2O
A hexagonal layered structure represented by YbGaMnO_4, characterized in that _3) are mixed at a molar ratio of approximately 1:2:1, and this mixture is heated at a temperature of 700°C or higher in a non-oxidizing atmosphere. A method for producing a compound having
JP6503881A 1981-04-27 1981-04-27 Compound having hexagonal layered structure represented by YbGaMnO↓4 and method for producing the same Expired JPS5933535B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6503881A JPS5933535B2 (en) 1981-04-27 1981-04-27 Compound having hexagonal layered structure represented by YbGaMnO↓4 and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6503881A JPS5933535B2 (en) 1981-04-27 1981-04-27 Compound having hexagonal layered structure represented by YbGaMnO↓4 and method for producing the same

Publications (2)

Publication Number Publication Date
JPS57179024A JPS57179024A (en) 1982-11-04
JPS5933535B2 true JPS5933535B2 (en) 1984-08-16

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ID=13275387

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Country Status (1)

Country Link
JP (1) JPS5933535B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04225713A (en) * 1990-12-26 1992-08-14 Ngk Insulators Ltd Combustion control method of waste incinerator

Also Published As

Publication number Publication date
JPS57179024A (en) 1982-11-04

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