JPH0338211B2 - - Google Patents
Info
- Publication number
- JPH0338211B2 JPH0338211B2 JP1750287A JP1750287A JPH0338211B2 JP H0338211 B2 JPH0338211 B2 JP H0338211B2 JP 1750287 A JP1750287 A JP 1750287A JP 1750287 A JP1750287 A JP 1750287A JP H0338211 B2 JPH0338211 B2 JP H0338211B2
- Authority
- JP
- Japan
- Prior art keywords
- compound
- oxide
- heated
- decomposes
- ybfeznmgo
- 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
Links
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 22
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 18
- 239000011701 zinc Substances 0.000 claims description 14
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 9
- 229910052742 iron Inorganic materials 0.000 claims description 9
- 229910052769 Ytterbium Inorganic materials 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 8
- 229910052725 zinc Inorganic materials 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 6
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- UZLYXNNZYFBAQO-UHFFFAOYSA-N oxygen(2-);ytterbium(3+) Chemical compound [O-2].[O-2].[O-2].[Yb+3].[Yb+3] UZLYXNNZYFBAQO-UHFFFAOYSA-N 0.000 claims description 4
- 239000011787 zinc oxide Substances 0.000 claims description 4
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 229910003454 ytterbium oxide Inorganic materials 0.000 claims description 3
- 229940075624 ytterbium oxide Drugs 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 claims description 2
- 239000000463 material Substances 0.000 description 7
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 5
- 239000000395 magnesium oxide Substances 0.000 description 5
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 5
- 239000000696 magnetic material Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000004065 semiconductor Substances 0.000 description 5
- 239000013078 crystal Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000000634 powder X-ray diffraction Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Description
産業上の利用分野
本発明は磁性材料,半導体材料及び触媒作用と
して有用な新規化合物であるYbFeZnMgO5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+O3)oFe2+O(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(FeO)1モルに対し
て、YbFeO3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 YbFeZnMgO 5 , which is a new compound useful as a magnetic material, a semiconductor material, and a catalytic material, and a method for producing the same. Conventional technology Conventionally, (Yb 3+ Fe 3+ O 3 ) o Fe 2+ O (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, Fe 2 O 2.5 layer. These compounds have a layered structure in which n moles of YbFeO 3 are combined with 1 mole of iron oxide (FeO).
【表】
発明の目的
本発明は(YbFeO3)oFeOの化学式において、
n=1/2に相当し、Fe2+の代わりに(Zn2++
Mg2+)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YbFeZnMgO5で示される化合物は、
イオン結晶モデルでは、Yb3+(Fe2+,Zn2+)
Mg2+O5 2-として記載され、その構造はYbO1.5
層,(Fe3+,Zn2+)O2.5層およびMgO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+は
Fe3+と共に(Fe3+,Zn2+)O2.5層を作り、Mg2+
はMgO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=3.400±0.001 (Å)
c=21.82±0.01 (Å)
この化合物の面指数(hKl),面間隔(d(Å))
(dpは実測値,dcは計数値を示す)及び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。
この化合物は磁性材料,半導体材料および触媒
材料として有用なものである。例えば異方性の強
い2次元的性質を持つ磁性体,半導体および触媒
物質としての利用の可能性が考えられる。[Table] Purpose of the invention The present invention is based on the chemical formula of (YbFeO 3 ) o FeO,
Corresponds to n = 1/2, and instead of Fe 2+ (Zn 2+ +
An object of the present invention is to provide a novel compound obtained by replacing Mg 2+ ). Constitution of the Invention The compound represented by YbFeZnMgO 5 of the present invention is
In the ionic crystal model, Yb 3+ (Fe 2+ , Zn 2+ )
Described as Mg 2+ O 5 2- , its structure is YbO 1.5
It is formed by laminating layers, (Fe 3+ , Zn 2+ )O 2.5 layers, and MgO layers, and one of its characteristics is that it has significant structural anisotropy. Zn 2+ is
Creates (Fe 3+ , Zn 2+ )O 2.5 layer with Fe 3+ and Mg 2+
creates an MgO layer. The lattice constants as a hexagonal crystal system are as follows. a=3.400±0.001 (Å) c=21.82±0.01 (Å) Planar index (hKl), plane spacing (d (Å)) of this compound
(d p is the measured value, d c is the counted value) and the relative reflection intensity (I (%)) for X-rays is shown in Table 2. This compound is useful as a magnetic material, a semiconductor material, and a catalytic material. For example, it is possible to use it as a magnetic material, a semiconductor, and a catalytic material that has two-dimensional properties with strong anisotropy.
【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、金属鉄あるいは酸化鉄もしくは
加熱により酸化鉄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、金属マグネシウムあるい
は酸化マグネシウムもしくは加熱により酸化マグ
ネシウムに分解される化合物とを、Yb,Fe,Zn
およびMgの割合が原子比で1対1対1対1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Feが各々
3価状態,ZnおよびMgが2価状態より還元され
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、磁性材料,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。
原料をそのまま、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,Fe,Zn,Mgの割合が
原子比で、1対1対1対1の割合であることが必
要である。これをはずず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Feが各々3価状態、ZnおよびMgが
各々2価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YbFeZnMgO5化合物の粉末は褐色で
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、YbO1.5層,(Fe,Zn)O2.5層,およびMgO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%以上の酸化イツテルビウム
(Yb2O3)粉末,純度99.9%以上の酸化鉄
(Fe2O3)粉末,試薬特級の酸化亜鉛(ZnO)お
よび試薬特級の酸化マグネシウム(MgO)粉末
をモル比で1対1対2対2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の微粉状混合物を得た。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急冷し
た。
得られた試料は、YbFeZnMgO5単一相であり、
粉末X線回折法によつて、各反射の面間隔(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次の通
りであつた。
a=3.400±0.001 (Å)
c=21.82±0.01 (Å)
上記の格子定数および表−2の各面指数(h
Kl)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ていた。
発明の効果
本発明は磁性材料,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. metal ytterbium or ytterbium oxide or a compound that decomposes into ytterbium oxide when heated; metal iron or iron oxide or a compound that decomposes into iron oxide when heated; metal zinc or zinc oxide or a compound that decomposes into zinc oxide when heated. Yb, Fe, Zn
and Mg in an atomic ratio of 1:1:1:1, and the mixture is heated at a temperature of 600°C or higher in the air, in an oxidizing atmosphere, or when Yb and Fe are in a trivalent state, Zn and Mg are each in a trivalent state. is obtained by heating in a reducing atmosphere in which the compound is not reduced from the divalent 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 a magnetic 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. Thoroughly mix the raw materials as they are or with alcohols, acetone, etc. The mixing ratio of the raw materials needs to be 1:1:1:1 in atomic ratio of Yb, Fe, Zn, and Mg. This naturally makes it impossible to obtain a single phase of the desired compound. This mixture is stored in the air, in an oxidizing atmosphere, or
In a reducing atmosphere where Yb and Fe are not reduced from their trivalent states, and Zn and Mg are not reduced from their divalent states.
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 YbFeZnMgO 5 compound powder was brown in color and was found to have a crystalline structure by powder X-ray diffraction. The crystal structure was found to be layered, consisting of 1.5 layers of YbO, 2.5 layers of (Fe, Zn)O, and a stack of MgO layers. Examples Ytterbium oxide (Yb 2 O 3 ) powder with a purity of 99.99% or more, iron oxide (Fe 2 O 3 ) powder with a purity of 99.9% or more, reagent grade zinc oxide (ZnO), and reagent grade magnesium oxide (MgO) The powder was weighed in a molar ratio of 1:1:2:2, ethanol was added in an agate mortar, and the mixture was 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 1300°C, and heated for 3 days, after which the sample was taken out of the furnace and rapidly quenched to room temperature. The obtained sample is YbFeZnMgO 5 single phase,
By powder X-ray diffraction method, the interplanar spacing of each reflection (d p )
The results of measuring the relative reflection intensity are shown in Table 2. The lattice constants as a hexagonal crystal system were as follows. a=3.400±0.001 (Å) c=21.82±0.01 (Å) The above lattice constant and each plane index (h
The interplanar spacing (d c (Å)) calculated from Kl) was in extremely good agreement with the actually measured interplanar spacing (d p (Å)). Effects of the Invention The present invention provides novel compounds useful as magnetic materials, semiconductor materials, and catalysts.
Claims (1)
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、金属鉄あるいは酸化鉄もしく
は加熱により酸化鉄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、金属マグネシウムある
いは酸化マグネシウムもしくは加熱により酸化マ
グネシウムに分解される化合物とを、Yb,Fe,
ZnおよびMgの割合が原子比で1対1対1対1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Feが
各々3価状態,ZnおよびMgが2価状態より還元
されない還元雰囲気中で加熱することを特徴とす
るYbFeZnMgO5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 YbFeZnMgO 5 . 2. Metallic ytterbium or yzterbium oxide or a compound that decomposes into ytterbium oxide when heated; Metallic iron or iron oxide or a compound that decomposes into iron oxide when heated; Metallic zinc or zinc oxide or a compound that decomposes into zinc oxide when heated. Yb, Fe,
Zn and Mg are mixed in an atomic ratio of 1:1:1:1, and the mixture is heated at a temperature of 600°C or higher in the air, in an oxidizing atmosphere, or when Yb and Fe are in the trivalent state, Zn and A method for producing a compound having a hexagonal layered structure represented by YbFeZnMgO 5 , which comprises heating in a reducing atmosphere in which Mg is not reduced beyond a divalent state.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1750287A JPS63185827A (en) | 1987-01-28 | 1987-01-28 | Compound, expressed by ybfeznmgo5 and having hexagonal layered structure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1750287A JPS63185827A (en) | 1987-01-28 | 1987-01-28 | Compound, expressed by ybfeznmgo5 and having hexagonal layered structure |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63185827A JPS63185827A (en) | 1988-08-01 |
JPH0338211B2 true JPH0338211B2 (en) | 1991-06-10 |
Family
ID=11945762
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1750287A Granted JPS63185827A (en) | 1987-01-28 | 1987-01-28 | Compound, expressed by ybfeznmgo5 and having hexagonal layered structure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63185827A (en) |
-
1987
- 1987-01-28 JP JP1750287A patent/JPS63185827A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS63185827A (en) | 1988-08-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |