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JPS5933536B2 - Compound having hexagonal layered structure represented by LuGaMnO↓4 and method for producing the same - Google Patents

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

Info

Publication number
JPS5933536B2
JPS5933536B2 JP9465781A JP9465781A JPS5933536B2 JP S5933536 B2 JPS5933536 B2 JP S5933536B2 JP 9465781 A JP9465781 A JP 9465781A JP 9465781 A JP9465781 A JP 9465781A JP S5933536 B2 JPS5933536 B2 JP S5933536B2
Authority
JP
Japan
Prior art keywords
compound
layered structure
producing
lugamno
structure represented
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
JP9465781A
Other languages
Japanese (ja)
Other versions
JPS57209831A (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 JP9465781A priority Critical patent/JPS5933536B2/en
Publication of JPS57209831A publication Critical patent/JPS57209831A/en
Publication of JPS5933536B2 publication Critical patent/JPS5933536B2/en
Expired legal-status Critical Current

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  • Inorganic Compounds Of Heavy Metals (AREA)

Description

【発明の詳細な説明】 本発明は新規化合物であるLuGaMnO4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, LuGaMnO4, having a hexagonal layered structure and a method for producing the same.

従来、YFe、04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 YFe, 04 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+OH−の化合物のY3+の代
りにLu3+ 、Fe2+ の代りにMn′+、Fe゜
+ の代わりにGa゜+ 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LuGaM
n04で示される化合物は、この化合物中、ルテチウム
はLu3+ 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、Lu3+Ga3+Mn
2+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 provides a novel compound in which Y3+ is replaced by Lu3+, Fe2+ is replaced by Mn'+, and Fe°+ is replaced by Ga°+ in the Y3+Fe2+Fe3+OH- compound, and a method for producing the same. LuGaM of the present invention
In the compound indicated by n04, lutetium exists as a Lu3+ ion, manganese exists as a Mn2+ ion, gallium exists as a trivalent ion, and Lu3+Ga3+Mn
It can be expressed as 2+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Lu、最小の黒丸はGa
とMnを示す。GaとMnはランダムに入つている。マ
ンガンの2価イオンとガリウムの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Lu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。
この結晶の面指数(hkl)、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。
This crystal has a hexagonal layered structure as shown in FIG. The largest circle is oxygen, the middle circle is Lu, and the smallest black circle is Ga.
and Mn. Ga and Mn are entered randomly. The divalent ions of manganese and the trivalent ions of gallium are surrounded by five-coordinated oxygen ions and occupy the same position crystallographically. Moreover, Lu has six-coordinated oxygen around it. Oxygen, an anion, has a dense structure.
Table 1 shows the plane index (hkl), plane spacing (dλ) (do indicates actual measurement, dc indicates calculated value), and relative reflection intensity (I%) for X-rays of this crystal.

そして空間群はR3″mで、その晶癖は板状晶で、格子
定数は次の通りである。a0=3.4273±O、00
01(λ)c0=25.824±O、002(λ)第1
表LuGaMn04 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 R3″m, the crystal habit is plate-like, and the lattice constant is as follows: a0=3.4273±O, 00
01 (λ) c0 = 25.824 ± O, 002 (λ) 1st
Table LuGaMn04 This compound is useful as a catalytic 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.

ルテチウム酸化物(LU2O3).マンガン酸化物(M
nO)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900℃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。本発明に用いるルテチウム酸化物は
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。
Lutetium oxide (LU2O3). Manganese oxide (M
nO) and gallium oxide (Ga2O3) in a molar ratio of approximately 1:2:1, and heating the mixture at a temperature of 900°C or higher in a non-oxidizing atmosphere. can. Commercially available lutetium 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.

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
常の試薬特級程度のものでよい。
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 of ordinary reagent grade level may be used.

粒径は前記、ルテチウム酸化物と同様な理由で10μm
以下であることが好ましい。また、1000℃で1f]
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7、0℃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10μm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LU2O3、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
英または白金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 10 μm for the same reason as the lutetium oxide mentioned above.
It is preferable that it is below. Also, 1f at 1000℃]
Preferably, the mixture is calcined in a mixed gas of carbon dioxide and hydrogen (mixing ratio: 1:1) and then rapidly cooled to 7.0°C, since the reaction speeds up. The gallium oxide may be of special reagent grade. As mentioned above, the particle size is preferably 10 μm or less. 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 LU2O3, MnO, . The molar ratio of Ga2O3 is 1:2:1. If this ratio is exceeded, the desired layered compound cannot be obtained. These mixtures are sealed in a quartz or platinum 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れて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900℃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約はない。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
LuGaMnO4化合物は黒色金属光沢を有し、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 be oxidized and become trivalent, so it is necessary to be in a non-oxidizing atmosphere. The heating temperature may be 900°C or higher, and the heating time is 10 minutes or more, preferably 1 hour or more. There are no restrictions on 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 LuGaMnO4 compound has a black metallic luster and is powder X.
It was found by line diffraction that it has a crystalline structure.

化合物中のマンガンイオンの価数は試料を空気中で加熱
する際の試料の重量変化を測定する重量分析法によつて
決定した。実施例 純度99.9%以上のルテチウム酸化物 (LU2O3)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(Ga2O3)粉末をモル比で1対2対1の割合
に秤量し、乳鉢内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 valence of manganese ions in the compound was determined by gravimetric analysis, which measures the change in weight of the sample when it is heated in air. Example Lutetium oxide (LU2O3) powder with a purity of 99.9% or more, manganese oxide (MnO) powder with a purity of 99.9% or more, and gallium oxide (Ga2O3) powder with a purity of 99.9% or more in a molar ratio of 1 The mixture was weighed at a ratio of 2:1, and acetone was added in a mortar and mixed thoroughly to obtain a fine powder mixture with an average particle size of several μm.

該混合物を白金管(内径8mm)内に入れて、電気熔接
法で溶封した。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4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Lu
GaMnO4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 platinum tube (inner diameter 8 mm) and sealed by electric welding. This was placed in a box-shaped siliconite furnace set at 1000°C and heated for about 4 days, after which the sample was taken out and rapidly cooled to room temperature. What was obtained was Lu
It was a hexagonal layered compound of GaMnO4. 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LuGaMnO4の結晶の図である。 The drawing is a diagram of a LuGaMnO4 crystal of the present invention.

Claims (1)

【特許請求の範囲】 1 LuGaMnO_4で示される六方晶系の層状構造
を有する化合物。 2 ルテチウム酸化物(Lu_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で900℃以上の温度で加熱する
ことを特徴とするLuGaMnO_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。
[Claims] 1. A compound having a hexagonal layered structure represented by LuGaMnO_4. 2 Lutetium oxide (Lu_2O_3), manganese oxide (MnO) and gallium oxide (Ga_2O_3
) in a molar ratio of approximately 1:2:1, and this mixture is heated at a temperature of 900°C or higher in a non-oxidizing atmosphere. A method for producing a compound having
JP9465781A 1981-06-19 1981-06-19 Compound having hexagonal layered structure represented by LuGaMnO↓4 and method for producing the same Expired JPS5933536B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9465781A JPS5933536B2 (en) 1981-06-19 1981-06-19 Compound having hexagonal layered structure represented by LuGaMnO↓4 and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9465781A JPS5933536B2 (en) 1981-06-19 1981-06-19 Compound having hexagonal layered structure represented by LuGaMnO↓4 and method for producing the same

Publications (2)

Publication Number Publication Date
JPS57209831A JPS57209831A (en) 1982-12-23
JPS5933536B2 true JPS5933536B2 (en) 1984-08-16

Family

ID=14116319

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9465781A Expired JPS5933536B2 (en) 1981-06-19 1981-06-19 Compound having hexagonal layered structure represented by LuGaMnO↓4 and method for producing the same

Country Status (1)

Country Link
JP (1) JPS5933536B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0583823U (en) * 1992-04-02 1993-11-12 サン ヤン イエオン Manuscript table

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0583823U (en) * 1992-04-02 1993-11-12 サン ヤン イエオン Manuscript table

Also Published As

Publication number Publication date
JPS57209831A (en) 1982-12-23

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