JP3288073B2 - Method for manufacturing catalyst member - Google Patents
Method for manufacturing catalyst memberInfo
- Publication number
- JP3288073B2 JP3288073B2 JP18850992A JP18850992A JP3288073B2 JP 3288073 B2 JP3288073 B2 JP 3288073B2 JP 18850992 A JP18850992 A JP 18850992A JP 18850992 A JP18850992 A JP 18850992A JP 3288073 B2 JP3288073 B2 JP 3288073B2
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- catalyst member
- molded body
- combustion
- organic binder
- 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 - Fee Related
Links
- 239000003054 catalyst Substances 0.000 title claims description 47
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 238000000034 method Methods 0.000 title claims description 9
- 239000011230 binding agent Substances 0.000 claims description 16
- 239000000835 fiber Substances 0.000 claims description 16
- 239000002002 slurry Substances 0.000 claims description 13
- 239000000919 ceramic Substances 0.000 claims description 12
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 9
- 239000004917 carbon fiber Substances 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 238000010304 firing Methods 0.000 claims description 5
- 238000004898 kneading Methods 0.000 claims description 5
- 238000005470 impregnation Methods 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 description 17
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 11
- 239000007789 gas Substances 0.000 description 8
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 238000000465 moulding Methods 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 4
- 239000002737 fuel gas Substances 0.000 description 4
- 239000001282 iso-butane Substances 0.000 description 4
- 229920000609 methyl cellulose Polymers 0.000 description 4
- 239000001923 methylcellulose Substances 0.000 description 4
- 235000010981 methylcellulose Nutrition 0.000 description 4
- 239000007788 liquid Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002245 particle 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
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- IXSUHTFXKKBBJP-UHFFFAOYSA-L azanide;platinum(2+);dinitrite Chemical compound [NH2-].[NH2-].[Pt+2].[O-]N=O.[O-]N=O IXSUHTFXKKBBJP-UHFFFAOYSA-L 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 1
- 238000007084 catalytic combustion reaction Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 229910052878 cordierite Inorganic materials 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 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 description 1
- 235000012438 extruded product Nutrition 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Press-Shaping Or Shaping Using Conveyers (AREA)
- Catalysts (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は燃焼用、排気ガス浄化用
などに用いられる触媒部材の製造方法に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a catalyst member used for combustion, exhaust gas purification, and the like.
【0002】[0002]
【従来の技術】従来、燃焼用、排気ガス浄化用などのた
めにコージライトなどのハムカム状セラミックスあるい
はコルゲート状セラミックスに触媒層を被覆していた。
また、ペーパーやフェルト状無機繊維を用途に合わせて
所定の形状に加工した後、触媒スラリーを被覆、担持し
て使用していた。2. Description of the Related Art Heretofore, a catalyst layer has been coated on a hamcam-like ceramic such as cordierite or a corrugated ceramic for combustion, purification of exhaust gas, and the like.
Further, after processing paper or felt-like inorganic fiber into a predetermined shape according to the application, the catalyst slurry is coated and carried before use.
【0003】[0003]
【発明が解決しようとする課題】前記ハニカム状セラミ
ックスやコルゲート状セラミックスの場合には外観形状
がきわめて制約され、一般に円形や角形に形成されてい
た。また、ペーパーやフェルト状無機繊維の場合でも所
定の形状に加工した後に触媒担持を行なうと、その形状
を加工する工程で形状に歪み、変形などが発生し易く生
産歩留まりが悪かった。In the case of the above-mentioned honeycomb-like ceramics and corrugated-like ceramics, the external shape is extremely restricted, and they are generally formed in a circular or square shape. Further, even when paper or felt-like inorganic fiber is processed into a predetermined shape and then loaded with a catalyst, the shape is easily deformed and deformed in the process of processing the shape, resulting in poor production yield.
【0004】本発明はこのような課題を解決するもの
で、所定の形状をした触媒部材を量産性よく加工できる
製造方法を提供することを目的とするものである。An object of the present invention is to solve such a problem, and an object of the present invention is to provide a manufacturing method capable of processing a catalyst member having a predetermined shape with good mass productivity.
【0005】[0005]
【課題を解決するための手段】この課題を解決するため
に本発明は、無機セラミックス繊維と有機バインダーと
を混練、押し出し成形、乾燥して一次成形体を得る工程
と、前記一次成形体を触媒スラリーに含浸、乾燥後、焼
成する工程とからなる触媒部材の製造方法を要旨とする
ものである。また本発明は、無機セラミックス繊維と有
機バインダーと炭素繊維あるいは炭素パウダーとを混
練、押し出し成形、乾燥して一次成形体を得る工程と、
前記一次成形体を触媒スラリーに含浸、乾燥後、焼成す
る工程とからなる触媒部材の製造方法を要旨とするもの
である。In order to solve this problem, the present invention provides a process for kneading inorganic ceramic fibers and an organic binder, extruding and drying to obtain a primary molded body.
If, impregnated with the primary molded body to the catalyst slurry, dried, it is an gist a method for manufacturing a catalyst member comprising a firing. Further, the present invention is a step of kneading an inorganic ceramic fiber and an organic binder and carbon fiber or carbon powder, extrusion molding, and drying to obtain a primary molded body,
Impregnating the primary molded body to the catalyst slurry, dried, it is an gist a method for manufacturing a catalyst member comprising a firing.
【0006】[0006]
【作用】上記構成の本発明によれば、無機セラミックス
繊維と有機バインダーとを適当な粘度に混練後、ダイス
で所定の形状に押し出し成形することによって量産性よ
く成形体を製造できる。得られた成形体は所望の長さに
切断し乾燥すると、この時点では有機バインダーで保形
されている。その後成形体を触媒スラリーに含浸し、乾
燥、焼成すると有機バインダーは焼失するが、成形体の
形状は触媒スラリー中に含まれる触媒粉末の凝集力(結
合力)で保持される。従って、得られた触媒部材の機械
的強度は成形体に付着される触媒粉末量、触媒粉末の粒
径あるいは触媒スラリー中に含まれる無機バインダーな
どにより決定される。According to the present invention having the above structure, a molded body can be manufactured with good mass productivity by kneading inorganic ceramic fibers and an organic binder to an appropriate viscosity and extruding the mixture into a predetermined shape with a die. When the obtained molded body is cut to a desired length and dried, at this point, the molded body is kept in an organic binder. After that, when the compact is impregnated with the catalyst slurry, dried and fired, the organic binder is burned off, but the shape of the compact is maintained by the cohesive force (coupling force) of the catalyst powder contained in the catalyst slurry. Therefore, the mechanical strength of the obtained catalyst member is determined by the amount of the catalyst powder attached to the molded body, the particle size of the catalyst powder, the inorganic binder contained in the catalyst slurry, and the like.
【0007】本発明は無機セラミックス繊維を使用して
多孔性に優れた(熱容量の小さな)触媒部材を量産的に
製造する方法である。押し出し成形体の多孔度は有機バ
インダーの添加量や成形条件(圧力、水など)を制御す
ることによってある程度任意に変更可能であるが、低コ
ストで多孔性に優れた触媒部材を生産するためには炭素
繊維あるいは炭素パウダー(特にピッチ系)を添加して
押し出し成形することが有効である。The present invention is a method for mass-producing a highly porous (small heat capacity) catalyst member using inorganic ceramic fibers. The porosity of the extruded product can be changed to some extent by controlling the amount of the organic binder added and the molding conditions (pressure, water, etc.). It is effective to add and extrude carbon fiber or carbon powder (particularly pitch-based).
【0008】[0008]
【実施例】以下、本発明の一実施例における触媒部材の
製造方法について、図面に基づいて説明する。 実施例1 アルミナシリカ繊維(繊維長5mm、繊維径約3μm)80
部とメチルセルロース(分子量4000)20部に少量の油脂
と水とを加え、混練した後、押し出し成形で図1に示す
ような成形体1を製造し、40℃で乾燥した。その後、図
2に示すように前記成形体1をAl2 O3 ・CeO2 粉
末(比表面積120 m2 /g)100 g、硝酸アルミニウム
4g、水500 g、イソプロピルアルコール50gおよびジ
ニトロジアンミン白金水溶液をPt換算で3g加えてな
る触媒スラリー液2(平均粒径1μm)に含浸後、図3
に示すように前記成形体1をアルミニウム構造体3に固
定し、80℃で20分間乾燥、400 ℃熱処理し、成形体1に
Ptを担持した触媒部材4を得るとともにこの触媒部材
4をアルミニウム構造体3に接着させた。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, a method for manufacturing a catalyst member according to an embodiment of the present invention will be described with reference to the drawings. Example 1 Alumina-silica fiber (fiber length 5 mm, fiber diameter about 3 μm) 80
A small amount of fats and oils and water were added to 20 parts by weight and 20 parts of methylcellulose (molecular weight: 4000), kneaded, and then extruded to produce a molded article 1 as shown in FIG. 1 and dried at 40 ° C. Then, as shown in FIG. 2, 100 g of Al 2 O 3 .CeO 2 powder (specific surface area: 120 m 2 / g), 4 g of aluminum nitrate, 500 g of water, 50 g of isopropyl alcohol, and an aqueous solution of dinitrodiammine platinum were used as shown in FIG. After impregnating in a catalyst slurry liquid 2 (average particle diameter 1 μm) obtained by adding 3 g in terms of Pt, FIG.
As shown in the figure, the compact 1 was fixed to an aluminum structure 3, dried at 80 ° C. for 20 minutes, and heat-treated at 400 ° C. to obtain a catalyst member 4 having Pt supported on the compact 1 and to attach the catalyst member 4 to an aluminum structure 3. It was adhered to body 3.
【0009】本実施例では有機バインダーとしてメチル
セルロース(分子量4000)を使用した。これはセルロー
ス系の有機バインダーが成形助剤として最も適している
からである。しかし低コスト化を図るためにはパルプも
使用可能である。In this embodiment, methylcellulose (molecular weight 4000) was used as an organic binder. This is because a cellulosic organic binder is most suitable as a molding aid. However, pulp can be used to reduce the cost.
【0010】次に上記アルミニウム構造体3に接着され
た触媒部材4を図4に示すように2個組み合わせ、図5
に示されるような燃焼装置を組み立てた。図5において
5はイソブタンガスボンベであり、このイソブタンガス
ボンベ5とノズル6の間にはバルブ7を設けてあり、ボ
ンベ5から供給された燃料ガスの流量をコントロールす
る。ノズル6より噴出した燃料ガスはガス流の誘引作用
により回りの空気を吸引し、混合室8で均一に混合し、
燃焼室9に供給される。燃焼室9はアルミニウム構造体
3壁面に密着した触媒部材4が2個組み合わさった状態
で構成され、アルミニウム構造体3の外壁面が発熱部10
となる。Next, two catalyst members 4 bonded to the aluminum structure 3 are combined as shown in FIG.
The combustion device as shown in was assembled. In FIG. 5, reference numeral 5 denotes an isobutane gas cylinder. A valve 7 is provided between the isobutane gas cylinder 5 and the nozzle 6, and controls the flow rate of the fuel gas supplied from the cylinder 5. The fuel gas ejected from the nozzle 6 sucks the surrounding air by the attraction of the gas flow, and is uniformly mixed in the mixing chamber 8.
It is supplied to the combustion chamber 9. The combustion chamber 9 is configured by combining two catalyst members 4 closely attached to the wall of the aluminum structure 3, and the outer wall of the aluminum structure 3 is
Becomes
【0011】次に上記構成の動作について説明する。ま
ず、ヒータ11が加熱され、近接する触媒部材4の一部が
高温化し、充分な活性温度に達した時点で、バルブ7が
開き、ノズル6より燃料ガスが混合室8に供給され、同
時に空気も誘引作用により供給される。燃料ガスと空気
は混合室8を経て燃焼室9に導入され、活性化したヒー
タ11近傍の触媒部材4から触媒燃焼を開始し、反応は次
第に燃焼室9内全体の触媒部材4に広がっていき、燃焼
ガスを排気口12から排出する。反応熱は燃焼排気ガスと
触媒部材4が接しているアルミニウム構造体3を経て外
部に提供される。Next, the operation of the above configuration will be described. First, when the heater 11 is heated and a part of the adjacent catalyst member 4 becomes high in temperature and reaches a sufficient activation temperature, the valve 7 is opened, and the fuel gas is supplied from the nozzle 6 to the mixing chamber 8, Is also supplied by the attraction. The fuel gas and air are introduced into the combustion chamber 9 through the mixing chamber 8 and start catalytic combustion from the activated catalyst member 4 near the heater 11, and the reaction gradually spreads to the entire catalyst member 4 in the combustion chamber 9. Then, the combustion gas is discharged from the exhaust port 12. The heat of reaction is provided to the outside via the aluminum structure 3 where the combustion exhaust gas and the catalyst member 4 are in contact.
【0012】イソブタンを燃料として空気過剰率(空気
/燃料)1.02、500Kcal /h の条件に設定し、排ガス
特性(HC、CO)から燃焼率を求めた。その結果、本
発明による実施例では燃焼率95%以上の燃焼特性が得ら
れた。Using isobutane as fuel, the excess air ratio (air / fuel) was set at 1.02, 500 Kcal / h, and the combustion rate was determined from the exhaust gas characteristics (HC, CO). As a result, in the example according to the present invention, a combustion characteristic of 95% or more was obtained.
【0013】実施例2 アルミナシリカ繊維(繊維長5mm、繊維径約3μm)80
部とピッチ系炭素繊維(繊維長3mm、繊維径約1μm)
10部とメチルセルロース(分子量4000)7部に少量の油
脂と水とを加え、混練した後、押し出し成形で図1に示
すような成形体1を製造した。その後成形体1を40℃で
乾燥した。その後成形体1をAl2 O3・CeO2 粉末
(比表面積120 m2 /g)100 g、硝酸アルミニウム4
g、水500 g、イソプロピルアルコール50gおよびジニ
トロジアンミン白金水溶液をPt換算で3g加えてなる
触媒スラリー液(平均粒径1μm)に含浸後、前記成形
体をアルミニウム構造体に固定し、80℃で20分間乾燥後
400 ℃熱処理し、成形体1にPtを担持した触媒部材を
得るとともにこの触媒部材をアルミニウム構造体に接着
させた。Example 2 Alumina-silica fiber (fiber length 5 mm, fiber diameter about 3 μm) 80
Part and pitch-based carbon fiber (fiber length 3mm, fiber diameter about 1μm)
A small amount of fats and oils and water were added to 10 parts and 7 parts of methylcellulose (molecular weight 4000), kneaded, and extruded to produce a molded article 1 as shown in FIG. Thereafter, the molded body 1 was dried at 40 ° C. Then, 100 g of Al 2 O 3 .CeO 2 powder (specific surface area: 120 m 2 / g), aluminum nitrate 4
g, 500 g of water, 50 g of isopropyl alcohol and 3 g of an aqueous solution of dinitrodiammine platinum in impregnated with a catalyst slurry (average particle size: 1 μm) obtained by adding 3 g in terms of Pt. After drying for a minute
A heat treatment was performed at 400 ° C. to obtain a catalyst member carrying Pt on the compact 1 and the catalyst member was bonded to the aluminum structure.
【0014】次に前記アルミニウム構造体に接着された
触媒部材を2個使用し、実施例1と同様にイソブタンの
燃焼排ガス特性(HC、CO)から燃焼率を求めた。そ
の結果、実施例2でも燃焼率95%以上の燃焼特性が得ら
れた。Next, using two catalyst members bonded to the aluminum structure, the combustion rate was determined from the combustion exhaust gas characteristics (HC, CO) of isobutane in the same manner as in Example 1. As a result, in Example 2, combustion characteristics of a combustion rate of 95% or more were obtained.
【0015】本実施例ではピッチ系炭素繊維を使用した
が、これによって有機バインダー(メチルセルロース)
の使用量を1/3にすることが可能となった。また、ピ
ッチ系炭素パウダーで押し出し成形を行なった場合にも
有機バインダー(メチルセルロース)の使用量約1/2
でほぼ同等な成形体を得ることができた。最終製品とし
て触媒部材とする場合には熱処理によって有機分を焼失
させるので、押し出し成形という成形手段のために使用
する成形助剤には安価な材料を選択して同等なものに加
工することが重要である。一般に成形助剤に使用する有
機バインダー(セルロース系)はピッチ系炭素繊維ある
いは炭素パウダーに比較すると高価であり、成形体の多
孔度を維持させるためにはピッチ系炭素繊維あるいは炭
素パウダーを効果的に使用することが好ましい。しか
し、無機セラミックス繊維とピッチ系炭素繊維あるいは
炭素パウダーだけで押し出し成形することは成形性が悪
く困難である。従って、有機バインダーもある程度添加
して成形することが不可欠である。In this embodiment, pitch-based carbon fibers are used.
Can be reduced to 1/3. Also, when extrusion molding is performed with pitch-based carbon powder, the amount of the organic binder (methyl cellulose) used is about 1/2.
As a result, substantially the same molded body could be obtained. When a catalyst material is used as the final product, the organic components are burned off by heat treatment.Therefore, it is important to select an inexpensive material and process it to an equivalent material for the molding aid used for the molding means called extrusion molding. It is. Generally, the organic binder (cellulose) used for the molding aid is more expensive than the pitch-based carbon fiber or carbon powder, and the pitch-based carbon fiber or carbon powder is effectively used to maintain the porosity of the molded article. It is preferred to use. However, extrusion molding using only inorganic ceramic fibers and pitch-based carbon fibers or carbon powder is difficult because of poor moldability. Therefore, it is indispensable to add an organic binder to some extent and to mold.
【0016】本実施例では、得られた触媒部材を燃焼用
として使用した例を示したが、本発明で得られる触媒部
材はさまざまな形状に加工できるのでその他いろいろな
用途でも利用できる。In this embodiment, an example in which the obtained catalyst member is used for combustion is shown. However, the catalyst member obtained in the present invention can be processed into various shapes and can be used for various other purposes.
【0017】[0017]
【発明の効果】以上のように本発明によれば、少なくと
も無機セラミックス繊維と有機バインダーとを混練、押
し出し成形、乾燥した後、触媒スラリーに含浸、乾燥、
焼成することにより、所望の形状をした多孔性に優れ、
熱容量の小さな触媒部材を量産性よく製造することが可
能である。また、炭素繊維や炭素パウダー使用すること
により高価な有機バインダーの使用量を少なくすること
が可能となる。As described above, according to the present invention, at least an inorganic ceramic fiber and an organic binder are kneaded, extruded and dried, then impregnated into a catalyst slurry, dried,
By firing, excellent porosity with the desired shape,
It is possible to produce a catalyst member having a small heat capacity with good mass productivity. In addition, the use of expensive organic binders can be reduced by using carbon fibers or carbon powder.
【図1】本発明の一実施例による触媒部材に用いる成形
体の斜視図FIG. 1 is a perspective view of a molded body used for a catalyst member according to one embodiment of the present invention.
【図2】同成形体を触媒スラリー液に含浸させる状態を
示す斜視図FIG. 2 is a perspective view showing a state in which the compact is impregnated with a catalyst slurry liquid.
【図3】同成形体にPtを担持して得た触媒部材をアル
ミニウム構造体に接着させた状態を示す斜視図FIG. 3 is a perspective view showing a state where a catalyst member obtained by supporting Pt on the molded body is bonded to an aluminum structure.
【図4】同アルミニウム構造体に接着された触媒部材を
2個組み合わせてなる燃焼装置の側断面図FIG. 4 is a side sectional view of a combustion device formed by combining two catalyst members bonded to the aluminum structure.
【図5】同燃焼装置の正面断面図FIG. 5 is a front sectional view of the combustion device.
1 成形体 2 触媒スラリー液 3 アルミニウム構造体 4 触媒部材 Reference Signs List 1 molded body 2 catalyst slurry liquid 3 aluminum structure 4 catalyst member
フロントページの続き (58)調査した分野(Int.Cl.7,DB名) B01J 21/00 - 38/74 C04B 38/00 - 38/10 Continuation of front page (58) Field surveyed (Int. Cl. 7 , DB name) B01J 21/00-38/74 C04B 38/00-38/10
Claims (2)
とを混練、押し出し成形、乾燥して一次成形体を得る工
程と、前記一次成形体を触媒スラリーに含浸、乾燥後、
焼成する工程とからなる触媒部材の製造方法。1. A process for kneading an inorganic ceramic fiber and an organic binder, extruding and drying to obtain a primary molded body.
And extent, impregnated with the primary molded body to the catalyst slurry, dried,
Method for producing a catalyst member comprising a firing.
と炭素繊維あるいは炭素パウダーとを混練、押し出し成
形、乾燥して一次成形体を得る工程と、前記一次成形体
を触媒スラリーに含浸、乾燥後、焼成する工程とからな
る触媒部材の製造方法。2. A step of kneading an inorganic ceramic fiber, an organic binder, and a carbon fiber or a carbon powder, extruding and drying to obtain a primary molded body;
I from the impregnation the catalyst slurry, dried, and firing
Method for producing that catalyst member.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18850992A JP3288073B2 (en) | 1992-07-16 | 1992-07-16 | Method for manufacturing catalyst member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18850992A JP3288073B2 (en) | 1992-07-16 | 1992-07-16 | Method for manufacturing catalyst member |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0631177A JPH0631177A (en) | 1994-02-08 |
JP3288073B2 true JP3288073B2 (en) | 2002-06-04 |
Family
ID=16224971
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18850992A Expired - Fee Related JP3288073B2 (en) | 1992-07-16 | 1992-07-16 | Method for manufacturing catalyst member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3288073B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2630546B2 (en) * | 1993-02-12 | 1997-07-16 | ニチアス株式会社 | Insulating sealing material and method for producing the same |
-
1992
- 1992-07-16 JP JP18850992A patent/JP3288073B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH0631177A (en) | 1994-02-08 |
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