JPH0333655B2 - - Google Patents

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Publication number
JPH0333655B2
JPH0333655B2 JP62129070A JP12907087A JPH0333655B2 JP H0333655 B2 JPH0333655 B2 JP H0333655B2 JP 62129070 A JP62129070 A JP 62129070A JP 12907087 A JP12907087 A JP 12907087A JP H0333655 B2 JPH0333655 B2 JP H0333655B2
Authority
JP
Japan
Prior art keywords
compound
oxide
heated
ybgazn
decomposes
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 - Lifetime
Application number
JP62129070A
Other languages
Japanese (ja)
Other versions
JPS63295428A (en
Inventor
Noboru Kimizuka
Naohiko Mori
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 JP12907087A priority Critical patent/JPS63295428A/en
Publication of JPS63295428A publication Critical patent/JPS63295428A/en
Publication of JPH0333655B2 publication Critical patent/JPH0333655B2/ja
Granted legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G15/00Compounds of gallium, indium or thallium
    • C01G15/006Compounds containing gallium, indium or thallium, with or without oxygen or hydrogen, and containing two or more other elements

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Catalysts (AREA)
  • Compounds Of Iron (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

産業上の利用分野 本発明は光機能材料、半導体材料及び触媒材料
として有用な新規化合物であるYbGaZn9θ12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。 従来技術 従来、(Yb3+Fe3+θ3)nFe2+θ(nは整数を示す)
で示される六方晶系の層状構造を有する化合物は
本出願人によつて合成され知られている。
YbFe2θ4、Yb2Fe3θ7、Yb3Fe4θ10及びYb4Fe5θ13
の六方晶系としての格子定数、Ybθ1.5層、Feθ1.5
層、Fe2θ2.5層の単位格子内における層数を示すと
表−1の通りである。 これらの化合物は酸化鉄(Feθ)1モルに対し
て、YbFeθ3がnモルの割合で化合していると考
えられる層状構造を持つ化合物である。
INDUSTRIAL APPLICATION FIELD The present invention relates to a compound having a hexagonal layered structure represented by YbGaZn 9 θ 12 , which is a new compound useful as an optical functional material, a semiconductor material, and a catalyst material, and a method for producing the same. Conventional technology Conventionally, (Yb 3+ Fe 3+ θ 3 )nFe 2+ θ (n indicates an integer)
The compound having a hexagonal layered structure represented by is synthesized by the applicant and is known.
YbFe 2 θ 4 , Yb 2 Fe 3 θ 7 , Yb 3 Fe 4 θ 10 and Yb 4 Fe 5 θ 13
Lattice constant as a hexagonal system, Ybθ 1.5 layers, Feθ 1.5
Table 1 shows the number of layers in the unit cell of Fe 2 θ 2.5 layers. These compounds have a layered structure in which n moles of YbFeθ 3 are combined with 1 mole of iron oxide (Feθ).

【表】 発明の目的 本発明は(YbFeθ3oFeθの化学式において、n
=1/9に相当しFe3+の代わりにGa3+をFe2+の代わ
りにZn2+を置きかえて得られる新規な化合物を
提供するにある。 発明の構成 本発明のYbGaZn9θ12で示される化合物は、イ
オン結晶モデルでは、Yb3+(Ga3+Zn2+
Zn8 2+θ12 2-として記載され、その構造はYbθ1.5層、
(Ga3+Zn2+)θ2.5層およびZnθ層の積層によつて形
成されており、著しい構造異方性を持つているこ
とがその特徴の一つである。Zn2+の1/9はGa3+
共に(Ga3+、Zn2+)θ2.5層を作り、残りの8/9は
Znθ層を作つている。六方晶系としての格子定数
は次の通りである。 a=3.296±0.001(Å) c=87.66±0.01(Å) この化合物の面指数(hkl)、面間隔(d(Å))
(dpは実測値、dcは計算値を示す)およびX線に
対する相対反射強度(I%)を示すと表−2の通
りである。 この化合物は光機能材料、半導体材料および触
媒材料等に有用なものである。
[Table] Purpose of the Invention The present invention is based on the chemical formula of (YbFeθ 3 ) o Feθ, where n
= 1/9 and is obtained by replacing Ga 3+ in place of Fe 3+ and Zn 2+ in place of Fe 2+. Structure of the Invention In the ionic crystal model, the compound represented by YbGaZn 9 θ 12 of the present invention is Yb 3+ (Ga 3+ Zn 2+ )
It is described as Zn 8 2+ θ 12 2- , and its structure consists of Ybθ 1.5 layers,
It is formed by laminating a (Ga 3+ Zn 2+ ) θ 2.5 layer and a Znθ layer, and one of its characteristics is that it has significant structural anisotropy. 1/9 of Zn 2+ forms a (Ga 3+ , Zn 2+ ) θ 2.5 layer with Ga 3+, and the remaining 8/9
Creates a Znθ layer. The lattice constants as a hexagonal crystal system are as follows. a=3.296±0.001 (Å) c=87.66±0.01 (Å) Planar index (hkl), interplanar spacing (d (Å)) of this compound
(d p is an actual measured value, d c is a calculated value) and the relative reflection intensity (I%) for X-rays is shown in Table 2. This compound is useful for optical functional materials, semiconductor materials, catalyst materials, and the like.

【表】【table】

【表】【table】

【表】 この化合物は次の方法によつて製造し得られ
る。 金属イツテルビウムあるいは酸化イツテルビウ
ムもしくは加熱により酸化イツテルビウムに分解
される化合物と、金属ガリウムあるいは酸化ガリ
ウムもしくは加熱により酸化ガリウムに分解され
る化合物と、金属亜鉛あるいは酸化亜鉛もしくは
加熱により酸化亜鉛に分解される化合物と、Yb、
GaおよびZnの割合が原子比で1対1対9の割合
で混合し、該混合物を600℃以上の温度で、大気
中、酸化性雰囲気中あるいはYbおよびGaが各々
3価イオン状態、Znが2価イオン状態より還元
されない還元雰囲気中で加熱することによつて製
造し得られる。 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、化学反応を速やかに進行さ
せるためには粒径が小さい方がよく、特に10μm
以下であることが好ましい。 また、光機能材料、半導体材料として用いる場
合には不純物の混入をきらうので、純度の高いこ
とが好ましい。出発物質が加熱により金属酸化物
を得る化合物としては、それぞれの金属の水酸化
物、炭酸塩、硝酸塩等が挙げられる。 原料はそのまま、あるいはアルコール類、アセ
トン等と共に充分に混合する。 原料の混合割合は、Yb、Ga及びZnの割合が原
子比で1対1対9の割合であることが必要であ
る。これをはずすと目的とする化合物の単一相を
得ることができない。 この混合物を大気中、酸化性雰囲気中あるいは
YbおよびGaが各々3価イオン状態、Znが各々2
価イオン状態から還元されない還元雰囲気中で
600℃以上で加熱する。加熱時間は数時間もしく
はそれ以上である。加熱の際の昇温速度には制約
はない。加熱終了後急冷するか、あるいは大気中
に急激に引き出せばよい。 得られたYbGaZn9θ12化合物の粉末は無色であ
り、粉末X線回折法によつて結晶構造を有するこ
とが分かつた。その結晶構造は層状構造であり、
Ybθ1.5層、(Ga、Zn)θ2.5層、およびZnθ層の積重
ねによつて形成されていることが分かつた。 実施例 純度99.99%以上の酸化イツテルビウム
(Yb2θ3)粉末、純度99.9%以上の酸化ガリウム
(Ga2θ3)粉末、試薬特級の酸化亜鉛(Znθ)粉末
をモル比で1対1対18の割合に秤量し、めのう乳
鉢内でエタノールを加えて、約30分間混合し、平
均粒径数μmの微粉末混合物を得た。該混合物を
白金管内に封入し、1450℃に設定された管状シリ
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、YbGaZn9θ12単一相であり、
粉末X線回折法によつて面指数(hkl)、面間隔
(dp)および相対反射強度を測定した結果は表−
2の通りであつた。 六方晶系としての格子定数は a=3.296±0.001(Å) c=87.66±0.01(Å) であつた。 上記の格子定数および表−2の面指数(hkl)
より算出した面間隔(dc(Å))は、実測の面間隔
(do(Å))と極めてよく一致していた。 発明の効果 本発明は光機能材料、半導体材料及び触媒とし
て有用な新規化合物を提供する。
[Table] This compound can be produced by the following method. Metallic ytterbium or ytterbium oxide or a compound that decomposes into ytterbium oxide by heating; Metallic gallium or gallium oxide or a compound that decomposes into gallium oxide by heating; Metallic zinc or zinc oxide or a compound that decomposes into zinc oxide by heating. Yb,
Ga and Zn are mixed in an atomic ratio of 1:1:9, and the mixture is heated at a temperature of 600°C or higher in the air, in an oxidizing atmosphere, or in an oxidizing atmosphere where Yb and Ga are each in a trivalent ion state and Zn is in a trivalent ion state. It can be produced by heating in a reducing atmosphere that does not reduce the divalent ion state. Commercially available starting materials used in the present invention may be used as they are, but in order for the chemical reaction to proceed quickly, it is better to have a small particle size, especially 10 μm.
It is preferable that it is below. Further, when used as an optical functional material or a semiconductor material, it is preferable to have high purity since contamination with impurities is avoided. Examples of compounds whose starting materials yield metal oxides by heating include hydroxides, carbonates, and nitrates of the respective metals. The raw materials are thoroughly mixed as they are or together with alcohols, acetone, etc. The mixing ratio of the raw materials needs to be such that the ratio of Yb, Ga, and Zn is in an atomic ratio of 1:1:9. If this is removed, a single phase of the target compound cannot be obtained. This mixture is stored in the air, in an oxidizing atmosphere, or
Yb and Ga are each in a trivalent ion state, Zn is each in a divalent state
In a reducing atmosphere that does not reduce from the valent ion state
Heat over 600℃. Heating time is several hours or more. There are no restrictions on the rate of temperature increase during heating. After heating, it can be rapidly cooled, or it can be rapidly drawn out into the atmosphere. The obtained YbGaZn 9 θ 12 compound powder was colorless and was found to have a crystalline structure by powder X-ray diffraction. Its crystal structure is layered,
It was found that it was formed by stacking a Ybθ 1.5 layer, a (Ga, Zn)θ 2.5 layer, and a Znθ layer. Example: Ytterbium oxide (Yb 2 θ 3 ) powder with a purity of 99.99% or more, gallium oxide (Ga 2 θ 3 ) powder with a purity of 99.9% or more, and reagent grade zinc oxide (Znθ) powder in a 1:1 molar ratio. The mixture was weighed at a ratio of 18:1, ethanol was added in an agate mortar, and mixed for about 30 minutes to obtain a fine powder mixture with an average particle size of several μm. The mixture was sealed in a platinum tube, placed in a tubular siliconite furnace set at 1450°C, and heated for 4 days, after which the sample was taken out of the furnace and rapidly cooled to room temperature. The obtained sample is YbGaZn 9 θ 12 single phase,
The results of measuring the plane index (hkl), plane spacing (d p ), and relative reflection intensity by powder X-ray diffraction are shown in Table-
2 was true. The lattice constants as a hexagonal crystal system were a=3.296±0.001 (Å) and c=87.66±0.01 (Å). The above lattice constants and the surface index (hkl) in Table 2
The calculated interplanar spacing (d c (Å)) was in excellent agreement with the actually measured interplanar spacing (do (Å)). Effects of the Invention The present invention provides novel compounds useful as optical functional materials, semiconductor materials, and catalysts.

Claims (1)

【特許請求の範囲】 1 YbGaZn9θ12で示される六方晶系の層状構造
を有する化合物。 2 金属イツテルビウムあるいは酸化イツテルビ
ウムもしくは加熱により酸化イツテルビウムに分
解される化合物と、金属ガリウムあるいは酸化ガ
リウムもしくは加熱により酸化ガリウムに分解さ
れる化合物と、金属亜鉛あるいは酸化亜鉛もしく
は加熱により酸化亜鉛に分解される化合物と、
Yb、GaおよびZnの割合が原子比で1対1対9の
割合で混合し、該混合物を600℃以上の温度で大
気中、酸化性雰囲気中あるいはYbおよびGaが
各々3価イオン状態、Znが2価イオン状態より
還元されない還元雰囲気中で加熱することを特徴
とするYbGaZn9θ12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] A compound having a hexagonal layered structure represented by 1 YbGaZn 9 θ 12 . 2 Metallic ytterbium or ytterbium oxide or a compound that decomposes into ytterbium oxide when heated; Metallic gallium or gallium oxide or a compound that decomposes into gallium oxide when heated; Metallic zinc or zinc oxide or a compound that decomposes into zinc oxide when heated. A compound that is
Yb, Ga, and Zn are mixed in an atomic ratio of 1:1:9, and the mixture is heated to a temperature of 600°C or higher in the air, in an oxidizing atmosphere, or when Yb and Ga are each in a trivalent ion state, Zn 1. A method for producing a compound having a hexagonal layered structure represented by YbGaZn 9 θ 12 , which comprises heating in a reducing atmosphere in which YbGaZn 9 θ 12 is not reduced to a divalent ion state.
JP12907087A 1987-05-26 1987-05-26 Compound having hexagonal layered structure represented by YbGaZn↓9O↓1↓2 and method for producing the same Granted JPS63295428A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12907087A JPS63295428A (en) 1987-05-26 1987-05-26 Compound having hexagonal layered structure represented by YbGaZn↓9O↓1↓2 and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12907087A JPS63295428A (en) 1987-05-26 1987-05-26 Compound having hexagonal layered structure represented by YbGaZn↓9O↓1↓2 and method for producing the same

Publications (2)

Publication Number Publication Date
JPS63295428A JPS63295428A (en) 1988-12-01
JPH0333655B2 true JPH0333655B2 (en) 1991-05-17

Family

ID=15000335

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12907087A Granted JPS63295428A (en) 1987-05-26 1987-05-26 Compound having hexagonal layered structure represented by YbGaZn↓9O↓1↓2 and method for producing the same

Country Status (1)

Country Link
JP (1) JPS63295428A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS606895A (en) * 1983-06-24 1985-01-14 株式会社東芝 Containment vessel

Also Published As

Publication number Publication date
JPS63295428A (en) 1988-12-01

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