JPH0545294B2 - - Google Patents
Info
- Publication number
- JPH0545294B2 JPH0545294B2 JP60090029A JP9002985A JPH0545294B2 JP H0545294 B2 JPH0545294 B2 JP H0545294B2 JP 60090029 A JP60090029 A JP 60090029A JP 9002985 A JP9002985 A JP 9002985A JP H0545294 B2 JPH0545294 B2 JP H0545294B2
- Authority
- JP
- Japan
- Prior art keywords
- honeycomb structure
- fine particles
- catalyst
- transition metal
- supported
- 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
Links
- 239000003054 catalyst Substances 0.000 claims description 31
- 239000010419 fine particle Substances 0.000 claims description 11
- 239000002131 composite material Substances 0.000 claims description 10
- 229910000314 transition metal oxide Inorganic materials 0.000 claims description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 6
- 229910010293 ceramic material Inorganic materials 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 238000010304 firing Methods 0.000 claims description 4
- 230000001070 adhesive effect Effects 0.000 claims description 3
- 238000002485 combustion reaction Methods 0.000 claims description 3
- 229910052878 cordierite Inorganic materials 0.000 claims description 2
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 238000000746 purification Methods 0.000 claims description 2
- 229910000505 Al2TiO5 Inorganic materials 0.000 claims 1
- AABBHSMFGKYLKE-SNAWJCMRSA-N propan-2-yl (e)-but-2-enoate Chemical compound C\C=C\C(=O)OC(C)C AABBHSMFGKYLKE-SNAWJCMRSA-N 0.000 claims 1
- 229910052845 zircon Inorganic materials 0.000 claims 1
- 230000000694 effects Effects 0.000 description 8
- 239000000843 powder Substances 0.000 description 6
- 238000010411 cooking Methods 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229910001111 Fine metal Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- -1 platinum group metals Chemical class 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- UFMZWBIQTDUYBN-UHFFFAOYSA-N cobalt dinitrate Chemical compound [Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O UFMZWBIQTDUYBN-UHFFFAOYSA-N 0.000 description 1
- 229910001981 cobalt nitrate Inorganic materials 0.000 description 1
- 239000012050 conventional carrier Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Catalysts (AREA)
Description
【発明の詳細な説明】
産業上の利用分野
本発明は燃焼に際発生する不完全燃焼成分、未
燃成あるいは各種調理の際発生する臭気の原因で
ある炭化水素成分を取り除くため燃焼機器内に設
けた排気ガス浄化触媒に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention provides a method for removing incompletely combusted components generated during combustion, unburned hydrocarbon components, or hydrocarbon components that cause odors generated during various types of cooking. The present invention relates to an exhaust gas purification catalyst provided therein.
従来の技術
従来この種の触媒体には各種のものが存在して
いた。すなわちその中でも最も一般的な白金族金
属を担持している触媒体は多孔質のセラミツク担
体に塩化白金酸水溶液の様な白金族金属を含んだ
水溶液を含浸させ、それを乾燥、焼成させて担体
細孔内の表面に金属微粒子としてあるいは金属酸
化物微粒子として付着させたものである。白金族
触媒は活性は良いが、コストが非常に高いのが欠
点である。遷移金属酸化物あるいは遷移金属を一
部取り込んだペロブスカイト複合酸化物はその粒
径を非常に小さくすれば白金並みの活性を持つこ
とは公知であるが、単独の遷移金属酸化物は高温
に不安定で、活性劣化につながるのに対し、ある
種のペロブスカイト構造を持つた複合酸化物は活
性も相当にあり、また耐性も有する。従つてこれ
らペロブスカイト化合物の微粉末を担体に付着さ
せれば優れた触媒体になるが、付着させた微粉末
はどうしても強度が弱く一部脱落しやすい。脱落
するのはほんの一部で活性劣化に及ぼす影響は少
ないが、黒色の多いペロブスカイト化合物が脱落
した後、白色の担体地肌がむき出しになり美観的
に好ましくない。特に家庭用燃焼機器にはこの問
題点を解決する必要がある。Prior Art Conventionally, there have been various types of catalyst bodies of this type. In other words, the catalyst supporting platinum group metals, which is the most common among them, is made by impregnating a porous ceramic carrier with an aqueous solution containing platinum group metals, such as an aqueous solution of chloroplatinic acid, and then drying and firing it. It is attached to the surface of the pores as fine metal particles or fine metal oxide particles. Although platinum group catalysts have good activity, their disadvantage is that they are very expensive. It is known that transition metal oxides or perovskite composite oxides incorporating a portion of transition metals have activity comparable to that of platinum if the particle size is made very small, but transition metal oxides alone are unstable at high temperatures. However, some composite oxides with a perovskite structure have considerable activity and are also resistant. Therefore, if fine powder of these perovskite compounds is attached to a carrier, it becomes an excellent catalyst, but the attached fine powder inevitably has low strength and tends to partially fall off. Only a small portion of the perovskite compound falls off, which has little effect on activity deterioration, but after the perovskite compound, which is mostly black, falls off, the white carrier surface becomes exposed, which is aesthetically undesirable. In particular, it is necessary to solve this problem for household combustion equipment.
発明が解決しようとする問題点
この様に従来の担体はほとんど白色あるいは白
色に近い色であり、付着していた黒色粉末が脱落
した場合どうしても目立つてしまう。本発明かか
る点に鑑みてなされたもので担体自身をあらかじ
め黒色、あるいは黒色に近い色にさせることを目
的としている。Problems to be Solved by the Invention As described above, conventional carriers are almost white or nearly white in color, and if the attached black powder falls off, it will be noticeable. The present invention has been made in view of this point, and its purpose is to make the carrier itself black or a color close to black in advance.
問題点を解決するための手段
本発明は上記問題点を解決するため、内部に微
小細孔を有した耐熱性セラミツク材料からなるハ
ニカム構造体と、このハニカム構造体の微小細孔
に担持される空気中で焼成すると黒色を呈する遷
移金属酸化物微粒子と、前記ハニカム構造体の外
表面に担持される酸化活性を有するペロブスカイ
ト複合酸化物の微粒子と、焼成することにより接
着性を有し前記遷移金属酸化物微粒子およびペロ
ブスカイト複合酸化物の微粒子を前記ハニカム構
造体に担持させる担持助剤とからなるものであ
る。Means for Solving the Problems In order to solve the above problems, the present invention provides a honeycomb structure made of a heat-resistant ceramic material having micropores inside, and a honeycomb structure supported by the micropores of the honeycomb structure. Transition metal oxide fine particles that exhibit a black color when fired in air; fine particles of perovskite composite oxide that has oxidizing activity and are supported on the outer surface of the honeycomb structure; and transition metal oxide particles that have adhesive properties when fired. The honeycomb structure is composed of oxide fine particles and a supporting agent for supporting the fine particles of perovskite composite oxide on the honeycomb structure.
作 用
本発明は上記した構成により担持された触媒粉
末が多少欠落しても、外観的には全く異常が認め
られない。また触媒担体内の細孔内部において遷
移金属酸化物を形成させるため、黒化させた触媒
担体は黒化させない触媒担体と比較して、触媒酸
化能力を大きく増大させることができる。Effects The present invention has the above-described structure, so even if some of the supported catalyst powder is missing, no abnormality is observed in appearance. Further, since transition metal oxides are formed inside the pores of the catalyst carrier, the blackened catalyst carrier can greatly increase the catalytic oxidation ability compared to the non-blackened catalyst carrier.
実施例
第1図は本発明の触媒体の一実施例を示すモデ
ル図である。第1図においては触媒担体、2は触
媒担体1内に存在する微小細孔で、その内壁面に
は遷移金属酸化物微粒子3が担持されている。触
媒担体1外表面4にはペロブスカイト複合酸化物
5を担持助剤の焼成によつてできるアルミナ6に
よつて強に付着されている。担持助剤にはコロイ
ダルアルミナや硝酸アルミニウムなど焼成するこ
とによつて多孔質で強固な接着性を有するものを
用いている。Embodiment FIG. 1 is a model diagram showing an embodiment of the catalyst body of the present invention. In FIG. 1, a catalyst carrier 2 is a micropore existing in the catalyst carrier 1, and transition metal oxide fine particles 3 are supported on the inner wall surface thereof. A perovskite composite oxide 5 is strongly adhered to the outer surface 4 of the catalyst carrier 1 by alumina 6 formed by firing a supporting agent. As the supporting agent, a material such as colloidal alumina or aluminum nitrate, which becomes porous and has strong adhesive properties by firing, is used.
上記の構成において触媒体の表面4が何等かの
機械的な衝撃あるいは接触で付着されているペロ
ブスカイト複合酸化物5とアルミナ6の皮膜の一
部が欠落しても、その下の地肌が黒色であるため
外観的には全く変ることがない。 In the above structure, even if part of the film of perovskite composite oxide 5 and alumina 6 attached to the surface 4 of the catalyst body is lost due to some mechanical impact or contact, the underlying surface will remain black. There is no change in appearance at all.
以下本触媒の作成法の一例を述べる。 An example of the method for producing this catalyst will be described below.
ペロブスカイト複合酸化物の微粒子(La0.9
Ce0.1C0O3)硝酸コバルト(C0(NO3)2・6H2O)
及び硝酸アルミニウム、(Al(NO3)3・9H2O)を
重量比で4:3:2の割合で混合させ、水を加え
スラリー状にする。さらにスラリーを安定なもの
にさせるためCMC、PVA等を若干加え所定の粘
度に調整したものゝ中に内部に微小細孔を有した
コーデイエライトのハニカム構造体を浸す。浸し
たハニカム構造体を取り出し、セル内内に留つた
スラリー液を風圧で吹き飛ばし、100℃で約1hr乾
燥した後、800℃で5min〜10min焼成を行なう。 Fine particles of perovskite composite oxide (La 0.9
Ce 0.1 C 0 O 3 ) Cobalt nitrate (C 0 (NO 3 ) 2・6H 2 O)
and aluminum nitrate (Al(NO 3 ) 3 ·9H 2 O) are mixed in a weight ratio of 4:3:2, and water is added to form a slurry. Furthermore, in order to stabilize the slurry, a small amount of CMC, PVA, etc. is added to adjust the viscosity to a specified level, and a cordierite honeycomb structure with micropores inside is immersed in the slurry. The immersed honeycomb structure is taken out, the slurry liquid remaining in the cells is blown away by wind pressure, dried at 100°C for about 1 hour, and then fired at 800°C for 5 to 10 minutes.
第2図は本発明の触媒担体の一応用例でガス調
理器内に触媒体を搭載した例である。 FIG. 2 is an example of the application of the catalyst carrier of the present invention, in which the catalyst body is mounted in a gas cooker.
ハニカム形状をした触媒体7を調理器庫内8の
上方にある排気ガス出口9に設置させてある。調
理庫内8の天面には金網発熱体10を置き、ガス
バーナ11により赤熱させるようになつている。
さらに調理器庫内8下部には調理物12を置くた
めの置き台13、調理物12からの油を受ける受
け皿14等が設置されている。 A catalyst body 7 having a honeycomb shape is installed at an exhaust gas outlet 9 above an interior 8 of the cooking appliance. A wire mesh heating element 10 is placed on the top surface of the cooking chamber 8, and is heated to red heat by a gas burner 11.
Furthermore, a stand 13 for placing the food 12 to be cooked, a saucer 14 for receiving oil from the food 12, etc. are installed in the lower part of the interior 8 of the cooking appliance.
上記の調理器において調理物12を置き台12
の上に置きガスバーナ11に点火させ、金網発熱
体10を赤熱させ、これから発生する輻射線及び
熱排気ガスにより調理物12を調理する。この際
調理物13から発生する臭気を含む炭化水素はガ
スバーナ11から発する排気ガスと共に排気ガス
出口9に設置されている触媒体7を通過し、炭化
水素は浄化される。 In the above cooker, the table 12 on which the food to be cooked 12 is placed
The gas burner 11 is placed on top of the device and the wire mesh heating element 10 is heated to red heat, and the food 12 is cooked by the radiation and hot exhaust gas generated from the wire mesh heating element 10. At this time, odor-containing hydrocarbons generated from the cooked food 13 pass through the catalyst body 7 installed at the exhaust gas outlet 9 together with the exhaust gas generated from the gas burner 11, and the hydrocarbons are purified.
発明の効果
本発明の触媒体の効果は次の通り、
(i) 微粉末の付着形の触媒体であるので、表面に
担持されているペロブスカイト微粉末が脱離し
ても、地肌が同色であるため美観的に見若しく
なく、特に家庭用燃焼器内に用いるには最適で
ある。Effects of the Invention The effects of the catalyst body of the present invention are as follows: (i) Since it is a catalyst body in which fine powder is attached, even if the perovskite fine powder supported on the surface is detached, the background color remains the same. Therefore, it is aesthetically unsightly and is especially suitable for use in household combustors.
(ii) 本発明の触媒体は触媒担体内の細孔内部に遷
移金属酸化物を形成させて黒化させるため、黒
化させない触媒担体を用いた触媒体に比較し
て、触媒能力を大きく増大させることができ
る。(ii) Since the catalyst body of the present invention forms transition metal oxides inside the pores of the catalyst carrier and causes blackening, the catalytic performance is greatly increased compared to a catalyst body using a catalyst carrier that does not blacken. can be done.
第1図は本発明の一実施例である触媒体の縦断
面図、第2図は同触媒体を調理器内に応用した縦
断面図である。
1……触媒担体、2……微小細孔、3……遷移
金属酸化物微粒子、5……ペロブスカイト複合酸
化物、6……アルミナ。
FIG. 1 is a longitudinal sectional view of a catalyst body according to an embodiment of the present invention, and FIG. 2 is a longitudinal sectional view of the catalyst body applied to a cooking appliance. DESCRIPTION OF SYMBOLS 1... Catalyst carrier, 2... Micropore, 3... Transition metal oxide fine particles, 5... Perovskite composite oxide, 6... Alumina.
Claims (1)
媒体において、内部に微小細孔を有した耐熱性セ
ラミツク材料からなるハニカム構造体と、このハ
ニカム構造体の微小細孔に担持される空気中で焼
成すると黒色を呈する遷移金属酸化物微粒子と、
前記ハニカム構造体の外表面に担持される酸化活
性を有するペロブスカイト複合酸化物の微粒子
と、焼成することにより接着性を有し前記遷移金
属酸化物微粒子およびペロブスカイト複合酸化物
の微粒子を前記ハニカム構造体に担持させる担持
助剤とからなる触媒体。 2 耐熱性セラミツク材料からなるハニカム構造
体は、コーデイエライト、α及びγアルミナ、ム
ライト−ジルコン、アルミニウムチタネートのい
ずれかで構成した特許請求の範囲第1項記載の触
媒体。[Scope of Claims] 1. A catalyst body for exhaust gas purification installed in a combustion device, which includes a honeycomb structure made of a heat-resistant ceramic material having micropores inside, and a honeycomb structure made of a heat-resistant ceramic material having micropores inside the honeycomb structure. Supported transition metal oxide fine particles that exhibit a black color when fired in air;
Fine particles of perovskite composite oxide having oxidizing activity supported on the outer surface of the honeycomb structure, and fine particles of transition metal oxide and fine particles of perovskite composite oxide having adhesive properties by firing are combined into the honeycomb structure. and a supporting agent supported on the catalyst. 2. The catalyst body according to claim 1, wherein the honeycomb structure made of a heat-resistant ceramic material is made of any one of cordierite, α and γ alumina, mullite-zircon, and aluminum titanate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60090029A JPS61249540A (en) | 1985-04-26 | 1985-04-26 | Catalyst |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60090029A JPS61249540A (en) | 1985-04-26 | 1985-04-26 | Catalyst |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61249540A JPS61249540A (en) | 1986-11-06 |
JPH0545294B2 true JPH0545294B2 (en) | 1993-07-08 |
Family
ID=13987245
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60090029A Granted JPS61249540A (en) | 1985-04-26 | 1985-04-26 | Catalyst |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61249540A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2597570B2 (en) * | 1987-03-20 | 1997-04-09 | 株式会社東芝 | High temperature combustion catalyst and method for producing the same |
KR100425254B1 (en) * | 2001-05-16 | 2004-03-30 | 한국표준과학연구원 | Nearly zero temperature coefficient of resistance in manganese nitride |
-
1985
- 1985-04-26 JP JP60090029A patent/JPS61249540A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61249540A (en) | 1986-11-06 |
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