JPS5943416B2 - Compound having hexagonal layered structure represented by YbFeZnO↓4 and method for producing the same - Google Patents

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

Info

Publication number
JPS5943416B2
JPS5943416B2 JP56065036A JP6503681A JPS5943416B2 JP S5943416 B2 JPS5943416 B2 JP S5943416B2 JP 56065036 A JP56065036 A JP 56065036A JP 6503681 A JP6503681 A JP 6503681A JP S5943416 B2 JPS5943416 B2 JP S5943416B2
Authority
JP
Japan
Prior art keywords
compound
iron
zinc
oxide
layered structure
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
JP56065036A
Other languages
Japanese (ja)
Other versions
JPS57179027A (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 JP56065036A priority Critical patent/JPS5943416B2/en
Publication of JPS57179027A publication Critical patent/JPS57179027A/en
Publication of JPS5943416B2 publication Critical patent/JPS5943416B2/en
Expired legal-status Critical Current

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  • Compounds Of Iron (AREA)
  • Hard Magnetic Materials (AREA)
  • Soft Magnetic Materials (AREA)

Description

【発明の詳細な説明】 本発明は、新規化合物であるYbFeZn0l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 YbFeZn0l 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、本出願人らによつて合成され、その存在
が既に知られている。
Conventionally, a compound having a hexagonal layered structure represented by YFe204 was synthesized by the present applicants, and its existence is already known.

この化合物は、Y奸Fe奸Fe奸042−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
オンによつて囲まれ、イットリウムYは、6配位の酸素
イオンをその周わわに持つている化合物であわ、磁性を
もつている。本発明は、前記、Y3YFe奸Fe奸04
奸化合物のY奸の代わわに、Yb奸Fe″Yの代わヤに
Zn叶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。
In this compound, the divalent and trivalent ions of iron are surrounded by five-coordinated oxygen ions, and yttrium Y is surrounded by six-coordinated oxygen It is a compound that has ions surrounding it and is magnetic. The present invention provides the above-mentioned Y3YFe奸Fe奸04
The object of the present invention is to provide a novel compound in which Zn is substituted for Yb, Fe''Y in place of Y in the compound, and a method for producing the same.

本発明のYbFeZn04で示される化合物は、この化
合物中、・鉄はFe3fイオン、イッテルビウムはYb
奸、亜鉛はZn叶として存在しておわ、Yb1Fe奸Z
n奸042−として表わすことができる。
In the compound represented by YbFeZn04 of the present invention, iron is Fe3f ion, ytterbium is Yb
Zinc exists as Zn, Yb1Fe Z.
It can be expressed as n奸042-.

この結晶は第1図に示すように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Fe
とZnを示している。FeとZnはランダムに分布して
いる。亜鉛の2価イオンと鉄の3価イオンは、5配位の
酸素イオンによつて囲まれている。結晶学的には同一の
位置を占めている。またYbは6配位の酸素をその周わ
クに持つている。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は単位格子内に於ける位置を示
す。この結晶の面指数hkL面間隔dlA)〔doは実
測、dcは計算値を示す。
This crystal has a hexagonal layered structure as shown in FIG. The largest circle is oxygen, the middle circle is Yb) The smallest black circle is Fe
and Zn. Fe and Zn are randomly distributed. The divalent ions of zinc and the trivalent ions of iron are surrounded by five-coordinated oxygen ions. Crystallographically, they occupy the same position. Moreover, Yb has hexacoordinated oxygen around it. Oxygen, an anion, has a dense structure. s, and u indicate the position within the unit cell. Planar index hkL plane spacing dlA) of this crystal [do indicates actual measurement, dc indicates calculated value.

〕、X−線に対する相対反射強度I済)は、第1表のと
おわである。空間群はR+nであ)、その晶癖は板状晶
であジ、格子定数は、次のと}bである。この化合物は
、磁性材料、半導体材料}よび触媒として有用なもので
ある。
], relative reflection intensity for X-rays) are as shown in Table 1. The space group is R+n), its crystal habit is plate-like, and its lattice constant is as follows. This compound is useful as a magnetic material, a semiconductor material, and a catalyst.

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.

金属イツテルビウムYbあるいは酸化イツテルビウムY
b2O3もしくは、加熱されることによつて酸化イツテ
ルビウムYb,O3に分解される化合物と、金属鉄ある
いは酸化鉄Fe2O3もしくは、加熱されることにより
酸化鉄Fe2O3に分解される化合物と亜鉛あるいは酸
化亜鉛ZnOもしくは加熱されることにより分解されて
酸化亜鉛ZnOを生ずる化合物とを、イツテルビウム、
鉄、亜鉛の割合が原子比で1対1対1になるように混合
して、1000℃以上の温度で、大気中、酸化性雰囲気
あるいは鉄および亜鉛が各々3価イオン状態、2価イオ
ン状態より還元されない程度の還元雰囲気のもとで加熱
することによつて製造することが出来る。
Metallic ytterbium Yb or ytterbium oxide Y
b2O3 or a compound that decomposes into ytterbium oxide Yb, O3 when heated, metallic iron or iron oxide Fe2O3, or a compound that decomposes into iron oxide Fe2O3 when heated and zinc or zinc oxide ZnO Or a compound that is decomposed by heating to produce zinc oxide ZnO, such as ytterbium,
Iron and zinc are mixed in an atomic ratio of 1:1:1, and at a temperature of 1000°C or higher, iron and zinc are dissolved in the air, in an oxidizing atmosphere, or in a trivalent ion state and a divalent ion state, respectively. It can be produced by heating in a reducing atmosphere that is less reducing.

本発明に用いる出発物質は、市販のものをそのまま使用
してもよいが、出発物質相互間の化学反応を速やかに進
行させるためには、粒径がちいさい程よく、特に10μ
m以下であることが好ましい。
As the starting materials used in the present invention, commercially available ones may be used as they are, but in order to rapidly advance the chemical reaction between the starting materials, the particle size should be as small as possible, especially 10 μm.
It is preferable that it is below m.

また磁性材料、電気材料として用いる場合には不純物の
混入をきらうので、出発原料物質は純度が高いほど好ま
しい。この原料をそのまま、あるいはアルコール類もし
くはアセトンと共に充分に混合する。これらの混合割合
は、イツテルビウム、鉄、亜鉛の割合が原子比として、
1対1対1の割合である。
Further, when used as a magnetic material or an electric material, since contamination with impurities is avoided, it is preferable that the starting material has a higher purity. This raw material is thoroughly mixed as is or with alcohol or acetone. The mixing ratio of these is the atomic ratio of itterbium, iron, and zinc.
The ratio is 1:1:1.

この割合をはずすと目的とする化合物を得ることは出来
ない。この混合物を大気中、あるいは酸化性雰囲気もし
くは鉄}よび亜鉛が3価イオン状態および2・価イオン
状態から還元され得ない程度の還元雰囲気のもとで、1
000℃以上の温度で加熱する。加熱時間は、1日もし
くはそれ以上である。加熱の際の昇温速度には制約はな
い。反応終了後は、0℃に急冷するかあるいは大気中に
急激にひきだせばよい。得られたYbFeZnO4化合
物は、茶褐色を示し、粉末X線回折法によつて、結晶構
造を有することがわかつた。その結晶構造は、既に本出
願人が得たYFe2O4と同型であることがわかつた。
出発混合試料と反応生成物の試料重量を精密に秤量し、
得られた試料の化学量論数を決定した。実施例 純度99.9%以上のイツテルビウム酸化物Yb2O3
粉末、純度99.9%以上の酸化銭Fe2O3粉末、}
よび試薬特級の酸化亜鉛ZnO粉末を、モル比で1対1
対1の割合に秤量し、乳鉢内でエチルアルコールを加え
て充分に混合し、平均粒径数μmの微粉末を得た。
If this ratio is exceeded, the target compound cannot be obtained. This mixture is heated in air or in an oxidizing atmosphere or in a reducing atmosphere such that iron and zinc cannot be reduced from their trivalent and divalent ion states.
Heating at a temperature of 000°C or higher. The heating time is one day 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 YbFeZnO4 compound exhibited a brown color and was found to have a crystalline structure by powder X-ray diffraction. It was found that its crystal structure was the same as that of YFe2O4, which had already been obtained by the applicant.
Precisely weigh the sample weights of the starting mixed sample and reaction product,
The stoichiometric number of the obtained sample was determined. Example Ytterbium oxide Yb2O3 with purity of 99.9% or more
Powder, oxidized Fe2O3 powder with purity of 99.9% or higher,}
and reagent grade zinc oxide ZnO powder in a 1:1 molar ratio.
The mixture was weighed at a ratio of 1:1, and ethyl alcohol was added in a mortar and thoroughly mixed to obtain a fine powder with an average particle size of several μm.

該混合物を白金ルツボ内にみたして、1309℃に設定
された箱型のシリコニツト炉内に入れ、4日間加熱し、
その後、試料を炉外にとりだし、室温まで急速に冷却し
た。得られた試料は、YbFeZnO4であり、既に報
告されているYFe2O4と結晶学的には、同型である
ことが粉末X線回折法によつて確認された。試料重量が
加熱前後で精密に秤量され、得られた試料の化学量論数
が決定された。第1表に得られた試料の結晶学的性質を
示した。
The mixture was placed in a platinum crucible, placed in a box-shaped siliconite furnace set at 1309°C, and heated for 4 days.
Thereafter, the sample was taken out of the furnace and rapidly cooled to room temperature. The obtained sample was YbFeZnO4, and it was confirmed by powder X-ray diffraction that it was crystallographically the same type as the previously reported YFe2O4. The weight of the sample was precisely weighed before and after heating, and the stoichiometry of the resulting sample was determined. Table 1 shows the crystallographic properties of the samples obtained.

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

図面は、本発明のYbFeZnO4結晶の図である。 The drawing is a diagram of the YbFeZnO4 crystal of the present invention.

Claims (1)

【特許請求の範囲】 1 YbFeZnO_4で示される六方晶系の層状構造
を有する化合物。 2 金属イッテルビウムYbあるいは酸化イッテルビウ
ムYb_2O_3もしくは、加熱されることにより酸化
イッテルビウムYb_2O_3に分解される化合物と、
金属鉄Feあるいは酸化鉄Fe_2O_3もしくは、加
熱されることにより酸化鉄Fe_2O_3に分解される
化合物と、亜鉛Znあるいは酸化亜鉛ZnOもしくは、
加熱されることにより分解されて酸化亜鉛ZnOを生ず
る化合物とを、イッテルビウム、鉄、亜鉛の割合が原子
比で1対1対1になるように混合して、1000℃以上
の温度で大気中、酸化性雰囲気あるいは鉄および亜鉛が
各各3価イオン状態、2価イオン状態より還元されない
程度の還元雰囲気のもとで加熱することを特徴とするY
bFeZnO_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 YbFeZnO_4. 2 metal ytterbium Yb or ytterbium oxide Yb_2O_3, or a compound that is decomposed into ytterbium oxide Yb_2O_3 by heating;
Metallic iron Fe or iron oxide Fe_2O_3 or a compound that is decomposed into iron oxide Fe_2O_3 by heating, and zinc Zn or zinc oxide ZnO or
A compound that is decomposed by heating to produce zinc oxide (ZnO) is mixed with ytterbium, iron, and zinc in an atomic ratio of 1:1:1, and the mixture is heated in the atmosphere at a temperature of 1000°C or higher. Y characterized by heating in an oxidizing atmosphere or a reducing atmosphere to the extent that iron and zinc are not reduced from their respective trivalent ion and divalent ion states.
A method for producing a compound having a hexagonal layered structure represented by bFeZnO_4.
JP56065036A 1981-04-27 1981-04-27 Compound having hexagonal layered structure represented by YbFeZnO↓4 and method for producing the same Expired JPS5943416B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56065036A JPS5943416B2 (en) 1981-04-27 1981-04-27 Compound having hexagonal layered structure represented by YbFeZnO↓4 and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56065036A JPS5943416B2 (en) 1981-04-27 1981-04-27 Compound having hexagonal layered structure represented by YbFeZnO↓4 and method for producing the same

Publications (2)

Publication Number Publication Date
JPS57179027A JPS57179027A (en) 1982-11-04
JPS5943416B2 true JPS5943416B2 (en) 1984-10-22

Family

ID=13275336

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56065036A Expired JPS5943416B2 (en) 1981-04-27 1981-04-27 Compound having hexagonal layered structure represented by YbFeZnO↓4 and method for producing the same

Country Status (1)

Country Link
JP (1) JPS5943416B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01123621U (en) * 1988-02-18 1989-08-23
JPH01123620U (en) * 1988-02-18 1989-08-23

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01123621U (en) * 1988-02-18 1989-08-23
JPH01123620U (en) * 1988-02-18 1989-08-23

Also Published As

Publication number Publication date
JPS57179027A (en) 1982-11-04

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