JPH0314778B2 - - Google Patents

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Publication number
JPH0314778B2
JPH0314778B2 JP62018919A JP1891987A JPH0314778B2 JP H0314778 B2 JPH0314778 B2 JP H0314778B2 JP 62018919 A JP62018919 A JP 62018919A JP 1891987 A JP1891987 A JP 1891987A JP H0314778 B2 JPH0314778 B2 JP H0314778B2
Authority
JP
Japan
Prior art keywords
compound
heating
oxide
decomposed
lutetium
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
JP62018919A
Other languages
Japanese (ja)
Other versions
JPS63185815A (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 JP1891987A priority Critical patent/JPS63185815A/en
Publication of JPS63185815A publication Critical patent/JPS63185815A/en
Publication of JPH0314778B2 publication Critical patent/JPH0314778B2/ja
Granted legal-status Critical Current

Links

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、半導体材料および触媒材
料として有用な新規化合物であるLuGaZn2O5
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+O3oFe2+0(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。 YbFe2O4、Yb2Fe3O7、Yb3Fe4O10及び
Yb4Fe5O13の六方晶系としての格子定数、YbO1.5
層、FeO1.5層、Fe2O2.5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FeO1モルに対して、
YbFeO3がnモル(n=1、2、3…)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 LuGaZn 2 O 5 , 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+ O 3 ) o Fe 2+ 0 (n indicates an integer)
The compound having a hexagonal layered structure represented by is synthesized by the applicant and is known. YbFe 2 O 4 , Yb 2 Fe 3 O 7 , Yb 3 Fe 4 O 10 and
Lattice constant of Yb 4 Fe 5 O 13 as hexagonal system, YbO 1.5
Table 1 shows the number of layers in the unit cell, FeO 1.5 layer, and Fe 2 O 2.5 layer. For 1 mole of iron oxide FeO, these compounds are
It is a compound with a layered structure that is thought to be composed of n moles of YbFeO 3 (n=1, 2, 3...).

【表】 発明の目的 本発明は(YbFeO3oFeOの化学式において、
n=1/2に相当し、Yb3+の代わりにLu3+を、Fe3+
の代わりにGa3+を、Fe2+の代わりにZn2+置きか
えて得られた新規な化合物を提供するにある。 発明の構成 本発明のLuGaZn2O5で示される化合物は、イ
オン結晶モデルではLu3+(Ga3+、Zn2+)Zn2+O5 2-
として記載され、その構造はLuO1.5層、(Ga3+
Zn2+)O2.5層およびZnO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ことがその特
徴の一つである。Zn2+イオンの半数はGa3+と共
に(Ga3+、Zn2+)O2.5層を作り、残りの半数は
ZnO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=3.365±0.001(Å) c=22.50±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、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 (YbFeO 3 ) o FeO,
Corresponds to n = 1/2, Lu 3+ instead of Yb 3+ , Fe 3+
The object of the present invention is to provide a novel compound obtained by replacing Ga 3+ in place of Fe 2+ and Zn 2+ in place of Fe 2+. Structure of the Invention In the ionic crystal model, the compound represented by LuGaZn 2 O 5 of the present invention is Lu 3+ (Ga 3+ , Zn 2+ )Zn 2+ O 5 2-
Its structure consists of 1.5 layers of LuO, (Ga 3+ ,
It is formed by laminating Zn 2+ )O 2.5 layers and ZnO layers, and one of its characteristics is that it has significant structural anisotropy. Half of the Zn 2+ ions form a (Ga 3+ , Zn 2+ ) O 2.5 layer with Ga 3+, and the other half
Creating a ZnO layer. The lattice constants as a hexagonal crystal system are as follows. a=3.365±0.001 (Å) c=22.50±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, etc.

【表】【table】

【表】 この化合物は次の方法によつて製造し得られ
る。 金属ルテチウムあるいは酸化ルテチウムもしく
は加熱により酸化ルテチ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を、Lu、Gaおよび
Znの割合が原子比で1対1対2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Lu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、Lu、Ga、及びZnの割合が
原子比で1対1対2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
LuおよびGaが各々3価イオン状態、Znが2価イ
オン状態から還元されない還元雰囲気中で600℃
以上のもとで加熱する。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LuGaZn2O5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、 LuO1.5層、(Ga、Zn)O2.5層、およびZnO層の
積み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%以上の酸化ルテチウム(Lu2O3
粉末、純度99.99%以上の酸化ガリウム(Ga2O3
粉末、および試薬特級の酸化亜鉛(ZnO)粉末を
モル比で1対1対4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、1300℃に設定された管状シリコ
ニツト炉内に入れ3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LuGaZn2O5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(I%)を測定した。その結果は表
−2の通りであつた。 六方晶系としての格子定数は a=3.365±0.001(Å) c=22.05±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
(dp(Å))と極めてよく一致した。 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 lutetium or lutetium oxide or a compound that is decomposed into lutetium oxide by heating; Metallic gallium or gallium oxide or a compound that is decomposed into gallium oxide by heating;
Metallic zinc or zinc oxide or a compound that is decomposed into zinc oxide by heating is
Mixing Zn at an atomic ratio of 1:1:2,
It can be produced by heating the mixture at a temperature of 600° C. or higher in the air, in an oxidizing atmosphere, or in a reducing atmosphere in which Lu and Ga are not reduced to a trivalent ion state and Zn is not reduced to a divalent ion state. It will be done. 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 Lu, Ga, and Zn is 1:1:2 in terms of atomic ratio. 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
600℃ in a reducing atmosphere where Lu and Ga are not reduced from the trivalent ion state and Zn from the divalent ion state.
Heat under the above conditions. 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 LuGaZn 2 O 5 compound powder was colorless and was found to have a crystal structure by powder X-ray diffraction. The crystal structure was found to be layered, consisting of 1.5 layers of LuO, 2.5 layers of (Ga, Zn)O, and a stack of ZnO layers. Example Lutetium oxide (Lu 2 O 3 ) with a purity of 99.99% or more
Powder, gallium oxide (Ga 2 O 3 ) with a purity of over 99.99%
Powder and reagent-grade zinc oxide (ZnO) powder were weighed at a molar ratio of 1:1:4, ethanol was added in an agate mortar, and the mixture was mixed for about 30 minutes to form a fine powder with an average particle size of several μm. A mixture was obtained. The mixture was sealed in a platinum tube, placed in a tubular siliconite furnace set at 1300°C, and heated for 3 days, and then the sample was taken out of the furnace and rapidly cooled to room temperature. The obtained sample was a single phase of LuGaZn 2 O 5 , and the planar index (hkl), interplanar spacing (d p ), and relative reflection intensity (I%) were measured by powder X-ray diffraction. The results were as shown in Table-2. The lattice constants as a hexagonal crystal system were a=3.365±0.001 (Å) and c=22.05±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 (d p (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 LuGaZn2O5で示される六方晶系の層状構造
を有する化合物。 2 金属ルテチウムあるいは酸化ルテチウムもし
くは加熱により酸化ルテチ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を、Lu、Gaお
よびZnの割合が原子比で1対1対2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Lu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
LuGaZn2O5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 LuGaZn 2 O 5 . 2 Metallic lutetium or lutetium oxide or a compound that is decomposed into lutetium oxide by heating; Metallic gallium or gallium oxide or a compound that is decomposed into gallium oxide by heating; and Metallic zinc or zinc oxide or a compound that is decomposed into zinc oxide by heating. and Lu, Ga, and Zn in an atomic ratio of 1:1:2, and the mixture was heated in the air at a temperature of 600°C or higher,
It is characterized by heating in an oxidizing atmosphere or in a reducing atmosphere in which Lu and Ga are not reduced to a trivalent ion state and Zn is not reduced to a divalent ion state.
A method for producing a compound having a hexagonal layered structure represented by LuGaZn 2 O 5 .
JP1891987A 1987-01-29 1987-01-29 Compound having hexagonal lamellar structure and expressed by lugazn2o5 and production thereof Granted JPS63185815A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1891987A JPS63185815A (en) 1987-01-29 1987-01-29 Compound having hexagonal lamellar structure and expressed by lugazn2o5 and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1891987A JPS63185815A (en) 1987-01-29 1987-01-29 Compound having hexagonal lamellar structure and expressed by lugazn2o5 and production thereof

Publications (2)

Publication Number Publication Date
JPS63185815A JPS63185815A (en) 1988-08-01
JPH0314778B2 true JPH0314778B2 (en) 1991-02-27

Family

ID=11985021

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1891987A Granted JPS63185815A (en) 1987-01-29 1987-01-29 Compound having hexagonal lamellar structure and expressed by lugazn2o5 and production thereof

Country Status (1)

Country Link
JP (1) JPS63185815A (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS606889A (en) * 1983-06-24 1985-01-14 Toshiba Corp Manufactur of scintillation type detector for x-ray ct device

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS606889A (en) * 1983-06-24 1985-01-14 Toshiba Corp Manufactur of scintillation type detector for x-ray ct device

Also Published As

Publication number Publication date
JPS63185815A (en) 1988-08-01

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