WO2004076027A1 - セラミックハニカム構造体 - Google Patents
セラミックハニカム構造体 Download PDFInfo
- Publication number
- WO2004076027A1 WO2004076027A1 PCT/JP2004/002373 JP2004002373W WO2004076027A1 WO 2004076027 A1 WO2004076027 A1 WO 2004076027A1 JP 2004002373 W JP2004002373 W JP 2004002373W WO 2004076027 A1 WO2004076027 A1 WO 2004076027A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ceramic
- surface roughness
- honeycomb structure
- pore diameter
- ceramic honeycomb
- Prior art date
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- 239000000919 ceramic Substances 0.000 title claims abstract description 183
- 239000011148 porous material Substances 0.000 claims abstract description 167
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- 239000003054 catalyst Substances 0.000 claims abstract description 46
- 238000000034 method Methods 0.000 claims abstract description 24
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052753 mercury Inorganic materials 0.000 claims abstract description 11
- 239000003566 sealing material Substances 0.000 claims description 63
- 239000010410 layer Substances 0.000 claims description 54
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical group [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 21
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- 239000007789 gas Substances 0.000 description 50
- 239000000843 powder Substances 0.000 description 38
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 34
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- 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 8
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- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 4
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- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 2
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- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 2
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
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- B01D46/2403—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies characterised by the physical shape or structure of the filtering element
- B01D46/2418—Honeycomb filters
- B01D46/2425—Honeycomb filters characterized by parameters related to the physical properties of the honeycomb structure material
- B01D46/2429—Honeycomb filters characterized by parameters related to the physical properties of the honeycomb structure material of the honeycomb walls or cells
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01D46/2425—Honeycomb filters characterized by parameters related to the physical properties of the honeycomb structure material
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- B01D46/2425—Honeycomb filters characterized by parameters related to the physical properties of the honeycomb structure material
- B01D46/24492—Pore diameter
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- B01D46/2418—Honeycomb filters
- B01D46/2451—Honeycomb filters characterized by the geometrical structure, shape, pattern or configuration or parameters related to the geometry of the structure
- B01D46/2466—Honeycomb filters characterized by the geometrical structure, shape, pattern or configuration or parameters related to the geometry of the structure of the adhesive layers, i.e. joints between segments
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- B01D46/2451—Honeycomb filters characterized by the geometrical structure, shape, pattern or configuration or parameters related to the geometry of the structure
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- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
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- B01D53/88—Handling or mounting catalysts
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- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
- B01J35/56—Foraminous structures having flow-through passages or channels, e.g. grids or three-dimensional monoliths
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
- C04B38/0006—Honeycomb structures
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/02—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust
- F01N3/021—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters
- F01N3/022—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters characterised by specially adapted filtering structure, e.g. honeycomb, mesh or fibrous
- F01N3/0222—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters characterised by specially adapted filtering structure, e.g. honeycomb, mesh or fibrous the structure being monolithic, e.g. honeycombs
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/02—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust
- F01N3/021—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters
- F01N3/033—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters in combination with other devices
- F01N3/035—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters in combination with other devices with catalytic reactors, e.g. catalysed diesel particulate filters
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
- F01N3/10—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
- F01N3/24—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by constructional aspects of converting apparatus
- F01N3/28—Construction of catalytic reactors
- F01N3/2803—Construction of catalytic reactors characterised by structure, by material or by manufacturing of catalyst support
- F01N3/2825—Ceramics
- F01N3/2828—Ceramic multi-channel monoliths, e.g. honeycombs
Definitions
- the present invention relates to a ceramic honeycomb structure effective as a filter or the like for removing particulates or the like in exhaust gas discharged from an internal combustion engine such as a diesel engine.
- Exhaust gas emitted from internal combustion engines such as vehicles such as buses and trucks and construction machinery contains particulates that harm the environment and the human body, and a technology to remove such particulates is required.
- a technology to remove such particulates is required.
- one of such technologies is a honeycomb structure for purifying exhaust gas (buinoleta) as shown in Fig. 1, which captures and removes particulates by passing exhaust gas through a porous ceramic member.
- a plurality of columnar porous ceramic members (units) 30 are combined via a sealing material layer 23 to form a ceramic block 25.
- a ceramic honeycomb filter 20 in which a sealing material layer 24 for preventing exhaust gas leakage is formed around the ceramic block 25.
- the through hole 31 formed in the porous ceramic member (unit) 30 has a sealing material 3 2 at one of the exhaust gas inlet and outlet ends. (Preferably in a pine pattern), and the exhaust gas flowing in from one end of one through-hole 31 passes through the partition wall 33 separating the through-hole 31, and then becomes adjacent. Through the other end of the through hole 31.
- the sealing material layer 24 provided on the outer periphery prevents the gas gas from leaking from the outer peripheral portion of the ceramic block 25 when the honeycomb filter 20 is installed in the exhaust passage of the internal combustion engine. It is provided for the purpose of prevention.
- Such a ceramic honeycomb filter 20 is currently used in a large vehicle, a vehicle equipped with a diesel engine, and the like because of its excellent heat resistance and easy regeneration processing.
- the honeycomb filter 20 for exhaust gas purification has conventionally been prepared by adjusting the pore diameter ⁇ pore distribution of the pores formed in the porous sintered body (partition wall), or by adjusting the wall thickness and the pore distribution.
- the mainstream is to adjust the trapping efficiency and pressure loss.
- the average pore diameter is;
- a diesel particulate filter in which the standard deviation of the pore diameter distribution is within 0.25 m and the pore diameter is expressed by a common logarithm of 0.20 or less.
- Reference 2 International Publication WOO 2/26351
- Reference 2 has an average pore diameter of 10 to 250 ⁇ m and a standard deviation of the pore diameter in which the pore diameter is expressed by a common logarithm is 0.40.
- the following catalyst-carrying filter is disclosed.
- Reference 3 Japanese Patent Application Laid-Open No. 2001-269522
- Japanese Patent Application Laid-Open Publication No. 2003-1029 discloses that the porosity of the cell wall is 55 to 75%, the average pore diameter is 10 to 40 ⁇ m, and the surface roughness (maximum height).
- a porous ceramic honeycomb filter having a Ry) of 10 ⁇ or more is disclosed.
- the exhaust gas filters disclosed in References 1 and 2 tend to have a low surface roughness because the pore size distribution of the filters is too uniform.
- the surface roughness is small, the surface roughness of the catalyst coating layer is also small, so that the reaction site between the catalyst coating layer and the particulates is reduced, and the supply of oxygen becomes insufficient.
- the catalytic reaction became insufficient.
- the distribution amount and the wall thickness of the pores are specified, and it is possible to provide fine pores for thin walls and large pores for thick walls.
- the surface roughness was substantially small, as in References 1 and 2, because substantially the same pores were dispersed at a uniform density.
- the honeycomb filter disclosed in Reference 4 has insufficient measures against pressure loss and the like because the pore distribution has not been studied. Disclosure of the invention
- the present invention has been made to solve the above-mentioned problems of the prior art, and it is an object of the present invention to provide an effective ceramic housing having excellent pressure loss and collection efficiency and high catalytic reactivity. It is to propose a structure of a two-cam structure.
- the inventors repeated experiments in which the pore-forming material added was adjusted in order to adjust the pore distribution in the ceramic honeycomb structure, and as a result, the pores measured by the mercury intrusion method were used. It was found that even if the distribution was in the same numerical range, there was a change in the burning characteristics of the particulates depending on the surface roughness of the partition walls and the thickness of the partition walls. In view of the above, the inventors have found that the ceramic honeycomb structure having a specified pore distribution in relation to the surface roughness of the partition wall and the thickness of the partition wall, even when a catalyst is supported on the partition wall surface, has a high surface roughness. Although it was somewhat reduced, it was found that there was no decrease in particulate collection efficiency and no increase in pressure loss. Based on such findings, the present invention was completed.
- the ceramic honeycomb structure of the present invention comprises:
- One or more pillar-shaped porous ceramic members are formed by arranging a large number of through holes in the longitudinal direction across the wall, and sealing one end of one of these through holes.
- the partition wall forming this structure with respect to the ceramic honeycomb structure comprising a combination of the following, has a surface roughness of 10 m or more at a maximum height roughness Rz specified in JIS B 0601-2001,
- the average pore size measured by the mercury intrusion method is 5 to: LOO / m, and the pore size is 0.9 to 1.1 times the average pore size.
- the ratio to the total pore volume is A (%) and the thickness of the partition wall is B ( ⁇ m)
- the present invention is not a technique for adjusting the pressure loss and the collection efficiency by simply controlling only the pore distribution measured by the mercury intrusion method as in the conventional technique.
- the reason for this is that simply adjusting the pore distribution on the partition wall surface, when coated with a catalyst, results in insufficient roughness of the partition wall surface as described above, deteriorating the reactivity of the catalyst. .
- the ceramic member for a honeycomb filter according to the present invention not only defines the pore distribution according to the wall thickness, but also has a surface roughness Rz in order to enhance the reactivity of the catalyst after the catalyst coating. We decided to do so.
- the surface of the porous ceramic member that partitions the through hole may be 100 zzm or less in terms of the maximum height roughness Rz specified in JISB0601-2001.
- a catalyst coating layer is preferably formed on the partition wall surface separating the through hole, and the porous ceramic portion
- the material is a silicon carbide ceramic
- the filter is used as a filter for an exhaust gas purification device of a vehicle. Preferably, it is used.
- the partition wall has a surface roughness of 10 / xm or more in terms of a maximum height roughness Rz specified in JISB 0601-2001, and
- the average pore diameter when the pore distribution is measured by the mercury intrusion method is 5 to: L 0 ⁇ m, and all pores having a pore diameter of 0.9 to 1.1 times the average pore diameter
- a (%) and the thickness of the partition wall is Bm
- the above equation (A ⁇ 90-B / 20) indicates that a certain relationship is established between the partition wall thickness and the pore distribution.For example, as the wall thickness becomes smaller, the average pore diameter becomes smaller. It is desirable to have relatively uniform pores with little variation and conversely, if the wall thickness is large, it is allowed to have a somewhat non-uniform pore size distribution with large variation with respect to the average pore diameter. Means By forming the partition walls based on such criteria, it is possible to improve each characteristic value of particulate collection efficiency and pressure loss.
- the collection efficiency of particulates means that if the wall thickness is small, it is collected only on the wall surface, but if the wall thickness is large, it is collected not only on the wall surface but also inside the wall. In this case, the particulate layer attached to the particulate wall surface becomes thinner, which not only increases the collection efficiency but also improves the overall Pressure loss is also reduced.
- the reaction efficiency is also affected by the wall thickness, that is, the reaction can be performed at the wall surface when the wall thickness is small, and even inside the wall when the wall thickness is large. Therefore, the greater the wall thickness, the higher the probability that the particulate exhaust gas comes into contact with the catalyst on the catalyst coat layer, so that the reactivity is improved.
- the wall thickness and the pore size distribution are determined based on the above equations.
- the surface roughness Rz of the partition wall indicated by the maximum height roughness be 10 ⁇ or more.
- a porous body has a surface roughness (irregularity) caused by the ceramic particles themselves, but the surface roughness is small.
- the particulates are composed of carbon fine particles, sulfur-based fine particles such as sulfate, high molecular weight hydrocarbon fine particles, etc., and even if the particle diameter is 20 to 70 O nm, Agglomeration often results in secondary particles of about 0.1 to 10 m.
- the paticle is filled in such a state that the paticles fill the gaps between the ceramic particles constituting the porous body and are densely packed in the pores on the surface.
- the pressure drop increases.
- the particulates which are hard to react due to agglomeration, are finely packed in the pores, so that there is a problem that the regeneration reaction does not easily occur.
- the surface roughness is made relatively large in order to improve the reactivity during regeneration.
- various flows occur in the exhaust gas, which makes it difficult for fine packing of particulates to occur.
- the inflow and outflow of the gas become intense, and the supply of oxygen and the like becomes easy to occur, and the catalytic reaction easily occurs. It is believed that ceramic members can be made.
- the surface roughness of the ceramic member In order to make the surface roughness of the ceramic member relatively large, the surface roughness of the wall after coating with the catalyst may be made relatively large.
- the second aspect of this effort is that the wall has a surface roughness with a maximum height roughness Rz of 10 / xm or more specified in JISB 0601-2001, and a finer surface by the mercury intrusion method.
- the average pore diameter is 5 to: L 00 m
- the ratio of the pores having a pore diameter 0.9 to 1.1 times the average pore diameter to the total pore volume is A (%)
- the thickness of the wall thickness is B (/ xm).
- a ceramic honeycomb structure characterized by satisfying the following.
- the above equation (A ⁇ l 00-B / 20) shows the relationship between the thickness of the partition wall and the pore distribution that affect the collection efficiency and the pressure loss, as in the first invention. It is desirable to have a relatively uniform pore distribution with less variation with respect to the average pore size as the thickness becomes thinner, and on the other hand, as the wall thickness increases, there is a somewhat uneven distribution with a large variation with respect to the average pore size. This means that a fine pore distribution is preferable. However, in this case, unlike the formula of the first invention, it is not preferable that the distribution of pores with respect to the wall thickness is too uniform.
- the above formula was conceived based on the finding that it is effective to intentionally create partial nonuniformity of pores by giving a certain degree of variation to the pore diameter. .
- the trapping efficiency and the pressure loss can be further improved, and the reactivity when the catalyst coat layer is formed can be improved.
- the aggregated secondary particles of the particulates are filled and adsorbed so as to cover the recesses, thereby reducing the surface roughness. Therefore, it is considered that the significance of the present invention in which the surface roughness is defined is lost, and the pressure loss increases and the reactivity deteriorates as in the related art. Further, in the present invention, when the catalyst coat layer is formed on the wall surface, the pore distribution is suppressed to be small, and when the surface roughness Rz is greater than 100, the pores of the filter are reduced. However, the catalyst coating layer is not formed deeply, and coating occurs, resulting in poor reactivity.
- the ceramic honeycomb structure according to the present invention includes a columnar porous ceramic member in which a large number of through holes are arranged in a longitudinal direction with a wall portion therebetween. May be constituted by binding a plurality of columnar porous ceramic members having a large number of through-holes arranged in parallel in the longitudinal direction with a partition wall interposed therebetween through a sealing material layer (hereinafter, referred to as an “assembly type”). It may be composed of a ceramic member integrally formed as a whole (hereinafter, referred to as “integrated honeycomb filter”).
- the wall portion is formed through a porous ceramic member.
- the integral honeycomb filter is composed of a partition separating the holes, and a sealing material layer functioning as an adhesive layer between the outer wall of the porous ceramic member and the porous ceramic member. It is composed of only partition walls.
- FIG. 1 is a perspective view schematically showing an example in which a ceramic honeycomb structure of the present invention is applied to a honeycomb filter.
- FIG. 2 (a) is a perspective view schematically showing one example of a porous ceramic member (unit) constituting the honeycomb filter shown in FIG. 1, and FIG. 2 (b) is a porous ceramic member.
- FIG. 3 is a sectional view taken along line A-A of the member.
- FIG. 3 (a) is a perspective view schematically showing an example in which the ceramic honeycomb structure of the present invention is applied to another form of a honeycomb filter
- FIG. 3 (b) is a perspective view of FIG. FIG. 2 is a sectional view taken along line BB of the filter shown in FIG.
- FIG. 4 is a diagram illustrating the roughness of the partition wall surface of the honeycomb filter of the present invention.
- FIG. 5 is a graph showing a relationship between a pore distribution ratio and a pressure loss in the filter according to the first embodiment.
- FIG. 6 is a graph showing a relationship between a pore distribution ratio and a collection efficiency in the filter according to the first embodiment.
- FIG. 7 is a graph showing the relationship between the surface roughness and the collection efficiency of the filter according to Example 1.
- FIG. 8 is a graph showing the relationship between the surface roughness and the regeneration rate of the filter according to the first embodiment.
- FIG. 9 is a graph showing the relationship between the surface roughness and the collection efficiency of the filter according to the first embodiment.
- FIG. 10 is a graph showing the relationship between the surface roughness and the regeneration rate of the filter according to the first embodiment.
- FIG. 11 shows the relationship between the pore distribution ratio and the pressure loss in the filter according to the second embodiment. It is a graph which shows a relationship.
- FIG. 12 is a graph showing a relationship between a pore distribution ratio and a collection efficiency in the filter according to the second embodiment.
- FIG. 13 is a graph showing the relationship between the surface roughness and the collection efficiency of the filter according to the second embodiment.
- FIG. 14 is a graph showing the relationship between the surface roughness and the regeneration rate of the filter according to the second embodiment.
- FIG. 15 is a graph showing the relationship between the surface roughness and the collection efficiency of the filter according to Example 2.
- FIG. 16 is a graph showing the relationship between the surface roughness and the regeneration rate in the filter according to Example 2.
- FIG. 17 is a graph showing a relationship between a pore distribution ratio and a pressure loss in the filter according to the third embodiment.
- FIG. 18 is a graph showing a relationship between a pore distribution ratio and a collection efficiency in the filter according to the third embodiment.
- FIG. 19 is a graph showing the relationship between the surface roughness and the collection efficiency of the filter according to Example 3.
- FIG. 20 is a graph showing the relationship between the surface roughness and the regeneration rate of the filter according to the third embodiment.
- FIG. 21 is a graph showing the relationship between the surface roughness and the collection efficiency of the filter according to Example 3.
- FIG. 22 is a graph showing the relationship between the surface roughness and the regeneration rate in the filter according to the third embodiment.
- FIG. 1 is a perspective view schematically showing a concrete example of an aggregated honeycomb filter which is an example of the honeycomb structure of the present invention
- FIG. 2 (a) is a honeycomb filter shown in FIG.
- FIG. 2 is a perspective view schematically showing an example of a porous ceramic member constituting a filter
- FIG. 2 (b) is a cross-sectional view of the porous ceramic member taken along line AA.
- a ceramic honeycomb structure (hereinafter, referred to as a “honeycomb filter”) 20 of the present invention has a plurality of porous ceramic members 30 bound together via a sealing material layer 23.
- a ceramic block 25 is formed, and around this ceramic block 25, a sealing material layer 24 for preventing leakage of exhaust gas is formed.
- the porous ceramic member 30 has a large number of through-holes 31 arranged in the longitudinal direction thereof, and one of the end portions on the exhaust gas inlet side and the outlet side is formed by a sealing material 32.
- the partition wall 33 that is sealed and separates these through holes 31 functions as a filter.
- the honeycomb filter 20 having such a configuration is installed as a filter in the exhaust passage of a fuel-burning engine such as a diesel engine, and the particulates of the exhaust gas discharged from the internal combustion engine pass through the honeycomb filter 20 when passing through the honeycomb filter 20.
- the exhaust gas is purified (wall flow type).
- the shape is cylindrical.
- the honeycomb structure of the present invention is not limited to a column.
- an elliptic column, a triangle, a square The shape may be a prism such as a hexagon.
- examples of the material of the porous ceramic member include nitride ceramics such as aluminum nitride, silicon nitride, boron nitride, and titanium nitride; silicon carbide; zirconium carbide; titanium carbide; tantalum carbide; Carbide ceramics such as tungsten carbide, and oxide ceramics such as alumina, zirconia, cordierite, and mullite are used. Among these, heat resistance is large, mechanical properties are excellent, strength, and thermal conductivity. Is also desirable.
- a silicon-containing ceramic mixed with metallic silicon a ceramic combined with silicon or a silicate compound, or the like can be used.
- silicon carbide ceramic refers to a material containing silicon carbide as a main component. Not only those made of silicon carbide but also those made of silicon carbide bonded with a metal, crystalline, or amorphous compound.
- the porous ceramic member preferably has a porosity (porosity) of about 20 to 80%, and more preferably 50 to 70%. The reason is that if the porosity is less than 20%, the honeycomb filter may immediately become clogged, while if the porosity exceeds 80%, the strength of the porous ceramic member decreases. This is because it is easily destroyed. When the catalyst is applied, the pressure loss increases sharply, so it is preferable to set the pressure loss to 50 to 70%.
- the porosity can be measured by a conventionally known method such as a mercury intrusion method, an Archimedes method, and a measurement using a scanning electron microscope (SEM).
- a conventionally known method such as a mercury intrusion method, an Archimedes method, and a measurement using a scanning electron microscope (SEM).
- the average pore diameter (diameter) of the porous ceramic member is desirably 5 to 100 ⁇ m. The reason is that if the average pore size is less than 5 in, the particulates can easily be clogged, while if the average pore size exceeds 100 im, the particulates pass through the pores. This is because the particulates cannot be collected and cannot function as a filter.
- the particle size of the ceramic used in producing such a porous ceramic member is not particularly limited, but preferably has a small shrinkage in the subsequent firing step, for example, 0.3 to 50 ⁇ m.
- a combination of 100 parts by weight of a powder having an average particle diameter of about m and 5 to 65 parts by weight of a powder having an average particle diameter of about 0.1 to 1.0 ⁇ m is desirable. This is because a porous ceramic member can be manufactured by mixing the ceramic powder having the above particle diameter with the above composition.
- the honeycomb structure has a structure in which both ends are sealed in order to collect particulates.
- the sealing material is desirably made of porous ceramic.
- the sealing material uses the same porous ceramic as the porous ceramic member. It is possible to increase the bonding strength between the two and to increase the porosity of the sealing material by the above-mentioned porous ceramic.
- the thermal expansion coefficient of the porous ceramic member and the thermal expansion coefficient of the encapsulant in the same manner as in the case of the encapsulant, it is possible to match the thermal expansion coefficient of the encapsulant with the encapsulant due to thermal stress during manufacturing and use. This is because it is possible to prevent a gap from being formed between the partition and the partition wall, and to prevent a crack from being generated in the partition between the sealing material and the sealing material.
- the sealing material is made of porous ceramic, for example, the same material as the above-described ceramic material constituting the porous ceramic member can be used.
- This sealing material can be formed by filling a ceramic powder into a slurry, or it can be formed by joining sealing pieces once manufactured. is there.
- the sealing material layer 23 is formed between the porous ceramic members 20, and the sealing material layer 24 is formed on the outer periphery of the ceramic block 25.
- the sealing material layer 23 formed between the porous ceramic members 30 functions as an adhesive for binding the plurality of porous ceramic members 30 together, while a seal formed on the outer periphery of the ceramic block 15
- the material layer 24 functions as a sealing material for preventing exhaust gas from leaking from the outer periphery of the ceramic block 25 when the filter 20 according to the present invention is installed in an exhaust passage of an internal combustion engine.
- an inorganic binder for example, an inorganic binder, an organic binder, a material made of inorganic fibers and / or inorganic particles, and the like are used.
- the sealing material layers are formed between the porous ceramic members or on the outer periphery of the ceramic block.
- these sealing material layers are made of the same material. And may be made of different materials. Further, when the sealing material layers are made of the same material, the compounding ratio of the materials may be the same or different.
- the inorganic binder for example, silica sol, alumina sol and the like are used. These may be used alone or in combination of two or more.
- silica sol is desirable.
- organic binder for example, polyvinyl alcohol, methyl cellulose, ethyl cellulose, carboxymethyl cellulose and the like are used. These may be used alone or in combination of two or more.
- carboxymethylcellulose is desirable.
- inorganic fibers for example, ceramic fibers such as silica-alumina, mullite, alumina, silica and the like are used. These may be used alone or in combination of two or more. Among the above inorganic fibers, silica-alumina fiber is desirable.
- the inorganic particles for example, carbides, nitrides, and the like are used. Specifically, inorganic powders made of silicon carbide, silicon nitride, boron nitride, or the like, whiskers, and the like are used. These may be used alone or in combination of two or more. Among the above inorganic particles, silicon carbide having excellent thermal conductivity is desirable.
- the sealing material layer 23 may be made of a dense body, and may be a porous body so that exhaust gas can flow into the inside thereof. It is desirable that it be made of a dense body. This is because the sealing material layer 24 is formed for the purpose of preventing the exhaust gas from leaking from the outer periphery of the ceramic block 25 when the filter 20 is installed in the exhaust passage of the internal combustion engine.
- FIG. 3 (a) is a perspective view schematically showing a specific example of an integrated filter which is an example of the honeycomb filter according to the present invention
- FIG. 3 (b) is a sectional view taken along line BB of FIG. .
- the honeycomb filter 10 is configured to include a columnar porous ceramic block 15 in which a large number of through holes 11 are arranged in the longitudinal direction with a wall 13 therebetween. Have been.
- the columnar porous ceramic block 15 has a large number of through-holes 11 arranged in the longitudinal direction thereof, and one of the exhaust gas inlet and outlet ends is filled with a filler 12.
- the partition 13 that is sealed and separates these through holes 11 functions as a filter.
- the honeycomb filter 10 has the same structure as the filter 20 except that the porous ceramic block 15 has an integral structure manufactured by sintering. After passing through the wall 13 that separates them, they flow out.
- the porosity (porosity) of the columnar porous ceramic block 15 is desirably 20 to 80%, and is preferably in the range of 50 to 70%. Is more desirable. The reason is that if the porosity of the porous ceramic block 15 is less than 20%, the filter 10 may immediately become clogged. On the other hand, the porosity of the porous ceramic block 15 may be 8 If it exceeds 0%, the strength of the filter 10 is reduced and the filter 10 may be easily broken. In particular, when the catalyst is applied, the pressure loss increases sharply.
- the size of the porous ceramic block 15 is not particularly limited, and is determined in consideration of the size of the exhaust passage of the internal combustion engine to be used.
- the shape is not particularly limited as long as it has a columnar shape.
- the shape may be a columnar shape, an elliptical columnar shape, a rectangular columnar shape, or the like, but usually, as shown in FIG. Is often used.
- porous ceramic constituting the porous ceramic block 15 examples include oxide ceramics such as cordierite, alumina, silica, and mullite, and carbides such as silicon carbide, zirconium carbide, titanium carbide, tantalum carbide, and tungsten carbide. Ceramics and nitride ceramics such as aluminum nitride, silicon nitride, boron nitride and titanium nitride are used, and usually, oxide ceramics such as cordierite are used. This is because it can be manufactured at low cost, has a relatively low coefficient of thermal expansion, and does not oxidize during use.
- the average pore diameter of the porous ceramic block 15 is desirably about 5 to 100 ⁇ m. The reason is that if the average pore diameter is less than 5 ⁇ m, the particulates can easily be clogged, while if the average pore diameter exceeds 100 m, the particulates pass through the pores. To collect the particulates. And cannot function as a filter.
- the sealing material in such a honeycomb filter 10 is desirably made of porous ceramic.
- porous ceramic By using the same porous ceramic as the porous ceramic block 15 as the sealing material, it is possible to increase the bonding strength between the two and to adjust the porosity of the sealing material so as to satisfy the above conditions.
- the thermal expansion coefficient of the porous ceramic block 15 and the thermal expansion coefficient of the sealing material can be matched, and the thermal stress during manufacturing or use can cause a gap between the sealing material and the wall 13. It is possible to prevent the occurrence of a gap and the occurrence of cracks in the sealing material and the wall portion 13 in contact with the sealing material.
- the sealing material is made of porous ceramic
- the material is not particularly limited.
- the same material as the ceramic material constituting the above-described porous ceramic block 15 can be used.
- the sealing material can be formed by filling a slurry of ceramic powder into a slurry, or the sealing material can be formed by joining the sealing pieces once manufactured. It is.
- a cross section perpendicular to the longitudinal direction of the through hole (hereinafter, simply referred to as a cross section) has a polygonal shape.
- the cross section of the through hole may be a polygon such as a quadrangle, a pentagon, an octagon or a trapezoid, or a mixture of various polygons.
- the above-mentioned raw material paste is continuously extruded from a metal die provided at the tip of the extruder and having many pores formed, and cut into a predetermined length. By doing so, a ceramic molded body is produced.
- the surface roughness of the formed body is adjusted to 100 ⁇ or less by performing a polishing treatment or the like on the forming pores of the die or the wall surface of the slit or the like. I do.
- the forming pores of the dies and the wall surfaces of the slits are the parts where the raw material paste comes into direct contact with the extrusion molding, and if the surface roughness of the wall surfaces is large, the ceramic molded body to be produced will The surface roughness of the partition wall surface in the through-hole becomes large, and it becomes difficult to adjust the surface roughness of the partition wall surface in the through-hole of the honeycomb filter manufactured through a post-process.
- the shape of the irregularities on the partition wall surface be adjusted by adjusting the aspect ratio of the pore-forming material having a pore-forming action.
- the shape of the irregularities on the partition wall surface can also be adjusted by adjusting the viscosity of the raw material paste, the particle size of each material, the mixing ratio, and the like.
- the raw material paste is not particularly limited as long as the porosity of the porous ceramic block after production becomes 20 to 80%.
- the binder and the dispersion of the ceramic powder as described above are used. What added a medium solution can be used.
- binder for example, methylcellulose, carboxymethylcellulose, hydroxyxeti "senorelose, polyethylene glycolone, phenol compound, epoxy resin and the like can be used. Usually, about 1 to 10 parts by weight is desirable with respect to 100 parts by weight of the ceramic powder.
- the dispersion medium liquid for example, an organic solvent such as benzene; alcohol such as methanol, water and the like can be used.
- This dispersion medium liquid is mixed in an appropriate amount so that the viscosity of the raw material paste falls within a certain range.
- the ceramic powder, the binder, and the dispersion medium are mixed by an attritor or the like, sufficiently kneaded with a kneader or the like, and then extruded to form the ceramic molded body. Further, a molding aid may be added to the raw material paste as needed.
- the molding aid for example, ethylene dalicol, dextrin, fatty acid stone, polyalcohol and the like are used.
- This raw material paste contains acid if necessary.
- a pore-forming agent such as a balloon, which is a micro hollow sphere containing a nitride ceramic as a component, a spherical acryl particle, and graphite may be added.
- the ceramic molded body is dried using a microwave drier, a hot air drier, a dielectric drier, a reduced pressure drier), a vacuum drier, a freeze drier, etc. Is filled with a sealing material paste to be a sealing material, and a sealing process is performed to plug the through hole.
- the sealing material paste is not particularly limited as long as the porosity of the sealing material manufactured through a post-process is 20 to 80%, and, for example, the same as the above-mentioned raw material paste However, it is preferable that a lubricant, a solvent, a dispersant, and a binder be added to the ceramic powder used in the raw material paste. This is because it is possible to prevent the ceramic particles in the sealing material paste from settling during the sealing process.
- the dried ceramic molded body filled with the above-mentioned sealing material paste is degreased and fired under predetermined conditions to form a filter made of porous ceramic, the whole of which is formed of one sintered body. To manufacture.
- conditions for degreasing and sintering the dried ceramic molded body are adjusted to increase the surface roughness.
- the pore-forming material, the molding aid, and the like may volatilize from the ceramic member and generate pores. At that time, a sufficient atmosphere is provided in the through-holes. It is necessary to pass gas.
- a raw material paste containing the above-described ceramic as a main component is formed into a formed body having a shape like the porous ceramic member 30 shown in FIG. 2 by extrusion molding.
- the above-mentioned “raw material paste” is the same as the raw material paste described in the aggregated honeycomb filter described above. The same thing as a strike can be mentioned.
- the formed form is dried using a microwave air dryer or the like to form a dried body, and a predetermined through hole of the dried body is filled with a sealing material paste serving as a sealing material.
- a sealing process for plugging the through hole is performed.
- the sealing material paste the same sealing material paste as that described in the integrated filter described above can be used; This can be performed in the same manner as in the case of the integrated filter.
- the dried body that has been subjected to the sealing treatment is degreased and fired under predetermined conditions to produce a porous ceramic member in which a plurality of through-holes are juxtaposed in the longitudinal direction across partition walls. be able to.
- the same method as in the case of the integrated filter described above can be used.
- the sealing material paste to be the sealing material layer 23 is applied in a uniform thickness, and the steps of sequentially laminating the other porous ceramic members 30 are sequentially repeated to obtain a prismatic shape having a predetermined size. A laminate of the porous ceramic member 30 is produced.
- the material constituting the sealing material paste is as described in the above-described filter of the present invention, and the description thereof is omitted here.
- the laminated body of the porous ceramic members 30 is heated to dry and solidify the sealing material paste layer to form the sealing material layer 24. Thereafter, for example, using a diamond force cutter or the like, Then, the outer peripheral portion is cut into a shape as shown in FIG. 1 to produce a ceramic block 25.
- a filter is formed in which a plurality of porous ceramic members are bound via the seal material layer. can do.
- the honeycomb filter 10 manufactured as described above when the honeycomb filter 10 manufactured as described above is mounted on the exhaust system of a diesel engine and used for a certain period of time, a large amount of particulates accumulate on the walls (partitions) of the honeycomb filter 10, Since the pressure loss increases, a regeneration process is performed. In this regeneration process, the gas heated by the heating means is caused to flow into the through-holes 11 of the two-cam filter 10 to heat the honeycomb filter 10, thereby forming a wall (partition wall). It burns and removes the particulates deposited on the surface. Further, the particulates may be burned and removed by using a post injection method.
- the honeycomb structure according to the present invention may increase the burning of particulates, and a catalyst may be carried on the partition wall surface in order to purify CO, HC, NOX and the like in exhaust gas.
- a catalyst may be carried on the partition wall surface in order to purify CO, HC, NOX and the like in exhaust gas.
- the honeycomb filter of the present invention functions as a filter for trapping particulates in the exhaust gas, and the above-described CO contained in the exhaust gas. It functions as a catalyst carrier for purifying HC, NOx and the like.
- the catalyst is not particularly limited as long as it can purify CO, HC, NOX and the like in the exhaust gas.
- a noble metal such as platinum, palladium or rhodium is used.
- alkali metals' group 1 of the periodic table
- alkaline earth metals group 2 of the periodic table
- rare earth elements group 3 of the periodic table
- transition metal elements etc.
- the portion supporting the catalyst on the partition wall surface of the honeycomb structure that is, the catalyst coat layer is a layer formed on the surface of each ceramic particle constituting the partition wall of the ceramic member.
- the catalyst made of the above-mentioned noble metal or the like can be used via a support material layer made of alumina, di / conia, titania, and silica having a high specific surface area.
- the alumina powder of the support material is finely pulverized with a powder frame machine or the like, and this is stirred and mixed with a solvent to produce a solution.
- an oxide powder such as alumina is produced by a sol-gel method or the like.
- the material has a specific surface area as high as possible to be used as a catalyst coating layer, and it is desirable to select a material having a high specific surface area value of 250 m 2 / g or more. Since the specific surface area is high, it is desirable to select ⁇ -alumina.
- an inorganic binder such as hydrated alumina, alumina sol, and silica sol may be added, pure water, water, phenol, diol, polyhydric phenol, ethylene glycol, ethylene oxide, triethanolamine, A solvent such as xylene is added in an amount of about 5 to 20 wt%, and the mixture is ground to about 500 nm or less and stirred.
- an alumina film can be uniformly formed on the partition wall particles of the ceramic member, unlike the catalyst coat layer formed by the conventional wet coat coated on the surface layer of the partition wall.
- the above-mentioned (metal) oxide powder-containing solution is impregnated. This is heated at 110 to 200 ° C. for about 2 hours to be dried, and then subjected to main firing.
- the preferable main firing temperature is 500 to: L0000 ° C, and the treatment is performed for 1 to 20 hours. If the temperature is lower than 500 ° C., crystallization does not proceed.On the other hand, if the temperature is higher than 100 ° C., the crystallization proceeds excessively and the surface area tends to decrease. . In addition, by measuring the weight before and after these steps, the amount of the supported substance can be calculated.
- the alumina impregnation Before the alumina impregnation, it is desirable to perform a treatment for improving the wettability on the surface of each particle on the partition wall of the ceramic member. For example, when the surface of the silicon carbide particles is modified with the HF solution, the wettability with the catalyst solution is changed, and the partition wall surface roughness after forming the catalyst coat layer becomes large.
- platinum is carried. After dropping the solution containing platinum, only the water absorption of the ceramic member, with a pipette, dry it at 110 ° C for 2 hours, and dry it at 500 to 100 ° C under a nitrogen atmosphere. It can be metallized.
- the use of the catalyst-carrying honeycomb filter of the present invention is not particularly limited, but is preferably used for an exhaust gas purification apparatus for a vehicle.
- Example 1 silicon carbide having different pore diameter, pore diameter distribution and surface roughness was used. A1 to A7, '', and ⁇ 1 to ⁇ 7 were fabricated to confirm the effects of forming a platinum-containing alumina coat layer on the surface of the ceramic member. is there. Table 1 shows the manufacturing conditions for each of these samples.
- the ceramic member according to Example 1 was manufactured through the following steps (1) to (5).
- a raw material (silicon carbide) powder having a relatively large average particle diameter hereinafter referred to as “powder ⁇ ”
- a raw material (silicon carbide) powder having a relatively small average particle diameter are used.
- methylcellulose as a molding aid was mixed at a predetermined ratio (wt%) with the silicon carbide raw material powder, and then a dispersion solvent composed of an organic solvent and water was added to knead all the raw materials. .
- extrusion molding is performed using a mold with a modified surface roughness of the slit of the mold so as to obtain a desired honeycomb shape, and a honeycomb molded body having a large number of through holes is formed. Eventually, a honeycomb molded body in which one end was sealed in a pine pattern was obtained.
- the molded body was dried at 150 ° C. and degreased at 500 ° C., and then under an inert gas atmosphere at a flow rate shown in Table 1 through the through-hole, Therefore the firing, a thickness of 3 0 0 m of the partition, the size is 3 4. in 3 mm X 3 4. 3 mm X 1 5 O mm, a cell density of 3 0 0 cells / in 2, the surface roughness Sample groups ⁇ 1 to ⁇ 7, ⁇ 1 to ⁇ 7,..., ⁇ 1 to ⁇ 7 of honeycomb-shaped ceramic members made of silicon carbide-based sintered bodies having different sizes were obtained.
- each sample manufactured by the above steps (1) to (5) was measured by a mercury intrusion method (according to JISR1655: 2003). Specifically, each sample of the ceramic member was cut into a cube of about 0.8 mm, After ultrasonic cleaning with ion-exchanged water, it was sufficiently dried.
- Each of such cut samples was measured using a micromeritics automatic porosimeter autopore # 9455 manufactured by Shimadzu Corporation.
- the measurement range is 0.2 to 50 ⁇ ⁇ ⁇ , where 100! In the range of ⁇ 500im, the pressure is measured at every 0.2psia, and 0.2 ⁇ ! In the range of 1100 ⁇ m, measurement was performed at a pressure of 0.25 psia.
- the average pore diameter (diameter) is calculated as 4 ⁇ S (integral pore area) / V (integral pore volume). From the average pore diameter, 0.9 to: Calculate the pore diameter of L. 1 times and calculate the ratio of the pore diameter range from the pore diameter distribution calculated from the measurement data to obtain the total pore diameter in the present invention. From the distribution and the average pore diameter, it becomes possible to calculate the ratio of the pore diameter of 0.9 to 1.1 times.
- each sample was cut so as to be parallel to the through hole, and the value of the surface roughness (indicated by the maximum height roughness Rz) of the partition in the center of each filter was measured.
- the measurement was performed using a machine (Surfcom 92 OA manufactured by Tokyo Seimitsu Co., Ltd.), and the measurement results are shown in Table 1.
- the initial pressure loss increases when the pore distribution is too dense, and the initial pressure loss also increases when the pore distribution is coarse.
- the pressure loss is smallest when the pore distribution is 80 to 90%, and similarly, when the wall thickness is 300 ⁇ m.
- the pressure loss was lowest when the pore distribution was 70 to 80%.
- 16 samples of each of the above C1 to C7, C1, to C7, and CI "to C7" are prepared, and the samples are bound together using a sealing material paste, and then cut with a diamond cutter.
- a honeycomb filter for exhaust gas purification was manufactured by forming a sealing material paste layer on the outer peripheral portion of the ceramic block using another sealing material paste. did.
- the specific manufacturing process is as follows.
- honeycomb-shaped ceramic member (sample) is bound using a heat-resistant sealing material paste containing 28.4% by weight of water, and then cut using a diamond cutter.
- the thickness of the sealing material layer for binding the ceramic member was adjusted to be 1.0 mm.
- a sealing material paste layer having a thickness of 1.0 mm was formed on the outer peripheral portion of the ceramic block using the adjusted sealing material paste. Then, the sealing material paste layer was dried at 120 ° C. to manufacture a cylindrical exhaust gas purifying honeycomb filter.
- samples having a pore distribution ratio of 85%, 80%, and 75% (A3 to A5, B3 to B5, C3 to C5, D3 to D5, E3 to E5), and of the extracted samples (A3, B3, C3, D3, E3) with a pore distribution ratio of 85%
- Samples (A3 ', B3,, C3, D3, E3,) with a thickness of 400 / m were prepared, and a sample (A5) with a pore distribution ratio of 75% was prepared.
- B5, C5, D5, and E5) samples (A5 " ⁇ B5" ⁇ C5 ", D5", E5,) with the wall thickness changed to 200 ⁇ m were prepared.
- sample groups (A3,, A4, A5 “), ( ⁇ 3 ', ⁇ 4, ⁇ 5 ,,), (C3,, C4, C5"), (D3,, D4, D5 ,, (E3, , E4, E5 “), dipped in 1% HF solution for 1 minute to form 60 g / L alumina coat layer, and 2 g ZL platinum (P t)
- a sample was prepared in which the catalyst was supported, and the surface roughness of the alumina coat layer after supporting the catalyst was also different, and the surface roughness after alumina coating and the initial pressure loss were measured for these samples.
- Measured Figure 9 shows the measurement results. As shown in this figure, the pressure loss tended to be high even if the surface roughness was high or low.
- Example 2 the pore size, the pore size distribution, and the surface roughness were changed.
- the ceramic member according to Example 2 was manufactured through the following steps (1) to (5).
- binder C Acrylic particles of various shapes (density: 1.1 g / cm 3 ) (hereinafter referred to as “powder C”) were used to produce ceramic members with the desired pore size distribution.
- Body A and powder B were mixed at a predetermined ratio (vol%) with respect to the raw material powder.
- methylcellulose as a molding aid was mixed with the raw material powder at a predetermined ratio (wt%), and a dispersion solvent composed of an organic solvent and water was added to knead all raw materials.
- extrusion molding is performed using a mold in which the surface roughness of the slits of the mold is changed so as to obtain a desired honeycomb shape, and a honeycomb formed body having a large number of through holes is formed.
- a honeycomb molded body having one end sealed in a checkered pattern was obtained.
- the molded body is dried at 150 ° C, degreased at 500 ° C, and then fired under an inert atmosphere while flowing the flow rates shown in Table 2 through the through holes.
- the thickness of the partition walls is 300 ⁇ ⁇
- the size is 34.3 mm ⁇ 34.3 mm ⁇ 150 mm
- the cell density is 300 cells / in 2 and the surface roughness is different.
- the sample groups F1 to F7, G1 to G7, ''', and J1 to J7 of the ceramic member of Example 1 were obtained.
- Example 2 For each of these samples, as in Example 1, the pore size distribution and surface roughness was measured, and the measurement results are shown in Table 2.
- samples ⁇ 1 to ⁇ 7 and HI "to H7" in which the wall thicknesses were changed to 400 ⁇ and 200 ⁇ , respectively were further prepared.
- gas was flowed at a cross-sectional flow rate of 5 m / s, and the initial pressure loss was measured. The results are shown in FIG. As shown in this figure, if the pore distribution is too dense, the initial pressure loss increases. In addition, the initial pressure loss is also high when it is coarse.
- the pressure loss is smallest when the pore distribution is 80 to 90%, and similarly, when the wall thickness is 300 ⁇ m.
- the pore distribution was 75 to 85% and the wall thickness was 400 m, the pressure loss was lowest when the pore distribution was 70 to 80%.
- each of the samples of ⁇ ⁇ 1 to ⁇ 7, ⁇ 1 'to ⁇ 7, and HI "to H7 was used to form a cylindrical filter (diameter 144 mm, porosity) using the same sealing material as in Example 1. (55%), and a diesel engine with a displacement of 300 cc was driven at a speed of 300 rpm and a torque of 4 ONm, and the exhaust gas discharged from the engine was filtered.
- the trapping efficiency was measured by allowing the sample to flow for 3 minutes and measuring the amount of trapped particulates before and after that (difference in the amount of trapped particles with and without a filter). As shown in this figure, it was found that when the wall thickness was large, a certain amount of trapped amount was secured even if the pore distribution was coarse.
- the wastewater was heated to 800 ° C, and a regeneration experiment after collecting 6 g / L was performed.
- the experimental results are shown in FIG. As shown in this figure, the regeneration rate was low between those having a large surface roughness and those having a low surface roughness, resulting in unburned residue. In the case of no surface modification, the surface roughness Rz was 10 ⁇ m or less.
- Example 2 in the ceramic structure in which the alumina coat layer in which the ceramic member carried 60 g / L of the catalyst was formed, when the soot was collected, the surface roughness was increased. It was found that when the Rz was 10 m or more, the regeneration efficiency was high when soot of 1 O g ZL was collected.
- Example 3 a group of ceramic members ⁇ 1 to ⁇ 7, ⁇ ', 01 to 07 of a cordierite ceramic member having different pore diameters, pore diameter distributions and surface roughness were prepared, and the surface of the ceramic member was prepared.
- the purpose of this study was to confirm the function and effect when a platinum-containing alumina coat layer was formed. Table 3 shows some of the manufacturing conditions for each of these samples.
- the ceramic member according to Example 3 was manufactured through the following steps (1) to (5). (1) First, talc (average particle size 10 / zm) 45wt% kaolin (average particle size 10 ⁇ ) 15wt% alumina (average particle size ⁇ ) 23wt% silica (average particle size ⁇ ) 17wty. was mixed.
- cordierite raw material powder This is named cordierite raw material powder.
- acrylic particles of various shapes density: 1. lg / cm 3 ) (this is referred to as “powder C”)
- the cordierite raw material powder was mixed at a predetermined ratio (vol%).
- methylcellulose as a molding aid was mixed at a predetermined ratio (wt%) with respect to the cordierite raw material powder, and a dispersion solvent composed of an organic solvent and water was added, and all the raw materials were kneaded. .
- extrusion molding is performed using a mold in which the surface roughness of the slit of the mold is changed so as to obtain a desired honeycomb shape, and a honeycomb molded body having a large number of through holes is formed.
- a honeycomb molded body in which one end was sealed in a pine pattern was obtained.
- the molded body is dried at 150 ° C and degreased at 500 ° C, and then fired in an inert gas atmosphere while flowing the flow rates shown in Table 3 through the through holes. Therefore, a honeycomb-shaped ceramic member made of cordierite with a wall thickness of 300 ⁇ , a size of 144 ⁇ X 15 Omm, a cell density of 300 cells / in 2 , a porosity of 55%, and a different surface roughness.
- Sample groups K1 to K7, L1 to L7, '*', and 01 to 07 were obtained.
- Example 3 For each of these samples, the pore size distribution and surface roughness were measured as in Example 1, and the results are shown in Table 3.
- the representative example is that the wall thickness is 3
- the sample M 1 whose wall thickness was changed to 400 m ⁇ and 200 m ' ⁇ M7, and Ml " ⁇ M7" were further fabricated, and using each sample with a different wall thickness as a filter, gas was flowed at a cross-sectional flow rate of 5 m / s, and the initial pressure loss was measured.
- FIG. As shown in this figure, if the pore distribution is too dense, the initial pressure loss increases. In addition, the initial pressure loss is also high when it is coarse.
- the pressure loss is smallest when the pore distribution is 80 to 90%, and similarly, when the wall thickness is 300 ⁇ .
- the pore distribution was 75 to 85% and the wall thickness was 400 ⁇ m, the pressure loss was lowest when the pore distribution was 70 to 80%.
- samples having a pore distribution ratio of 85%, 80%, and 75% K3 to K5, L3 to L5, M3 to M5, N3 to N5, 03 to 05), and samples (K3, L3, M3, N3, 03) with a pore distribution ratio of 85% among the extracted sample
- Samples (K3,, L3 ', M3,, N3,, 03,) with a thickness changed to 400 ⁇ were prepared, and a sample (K5 , L5, M5, N5, 05), samples (K5 ′′, L5 ′′, M5 ′′, N5 ′′, 05 ′′) were prepared with the wall thickness changed to 200 ⁇ m.
- sample groups K3,, ⁇ 4, "5"), (L3,, L4, L5 ,,), (M3,, M4, M5 “), (N3,, N4, N5" (03,, 04, 05 ") were immersed in a 0.1% hydrochloric acid solution for 1 minute to form a 60 g / L alumina coat layer, and 2 g / L platinum (P t)
- P t platinum
- a sample was prepared in which the catalyst was supported, and the surface roughness of the alumina coat layer after the catalyst support was also different. These samples were evaluated for the surface roughness after alumina coating and the initial pressure loss.
- the measurement results are shown in Fig. 21. As shown in this figure, there was a tendency for the pressure loss to be high regardless of whether the surface roughness was high or low.
- the surface roughness Rz It was found that the regeneration efficiency was high when 10 g ZL of soot (soot) was collected when the value was 10 ⁇ or more.
- the ceramic honeycomb structure of the present invention is used for an engine using fossil fuel, such as a diesel engine, or an exhaust gas conversion device for a boiler.
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Abstract
Description
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
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AT04715472T ATE481151T1 (de) | 2003-02-28 | 2004-02-27 | Keramische wabenstruktur |
EP04715472A EP1598102B1 (en) | 2003-02-28 | 2004-02-27 | Ceramic honeycomb structure |
JP2005502950A JP4516017B2 (ja) | 2003-02-28 | 2004-02-27 | セラミックハニカム構造体 |
DE602004029140T DE602004029140D1 (de) | 2003-02-28 | 2004-02-27 | Keramische wabenstruktur |
KR1020057008442A KR100632161B1 (ko) | 2003-02-28 | 2004-02-27 | 세라믹 하니컴 구조체 |
US10/527,531 US7504359B2 (en) | 2003-02-28 | 2004-02-27 | Ceramic honeycomb structure |
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JP2003-053724 | 2003-02-28 | ||
JP2003053724 | 2003-02-28 |
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WO2004076027A1 true WO2004076027A1 (ja) | 2004-09-10 |
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PCT/JP2004/002373 WO2004076027A1 (ja) | 2003-02-28 | 2004-02-27 | セラミックハニカム構造体 |
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US (1) | US7504359B2 (ja) |
EP (1) | EP1598102B1 (ja) |
JP (2) | JP4516017B2 (ja) |
KR (1) | KR100632161B1 (ja) |
CN (1) | CN1326593C (ja) |
AT (1) | ATE481151T1 (ja) |
DE (1) | DE602004029140D1 (ja) |
WO (1) | WO2004076027A1 (ja) |
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DE60317174T3 (de) * | 2002-03-22 | 2013-01-17 | Ibiden Co., Ltd. | Herstellungsverfahren eines wabenfilters zur reinigung von abgas |
DE20321503U1 (de) * | 2002-09-13 | 2007-08-30 | Ibiden Co., Ltd., Ogaki | Wabenstrukturkörper |
JP4200430B2 (ja) * | 2003-02-18 | 2008-12-24 | トヨタ自動車株式会社 | 排ガス浄化フィルタ触媒用基材の良否判別方法 |
US7504359B2 (en) | 2003-02-28 | 2009-03-17 | Ibiden Co., Ltd. | Ceramic honeycomb structure |
DE602004011997T2 (de) | 2003-06-05 | 2009-02-26 | Ibiden Co., Ltd., Ogaki | Wabenkörperstruktur |
US20060051556A1 (en) * | 2003-09-12 | 2006-03-09 | Ibiden Co., Ltd. | Sintered ceramic compact and ceramic filter |
ATE386581T1 (de) * | 2003-10-20 | 2008-03-15 | Ibiden Co Ltd | Wabenstruktur |
EP1632657B1 (en) | 2003-11-05 | 2013-08-21 | Ibiden Co., Ltd. | Method of producing honeycomb structure body |
US7387829B2 (en) * | 2004-01-13 | 2008-06-17 | Ibiden Co., Ltd. | Honeycomb structure, porous body, pore forming material for the porous body, and methods for manufacturing the pore forming material, the porous body and the honeycomb structure |
JPWO2005108328A1 (ja) * | 2004-05-06 | 2008-03-21 | イビデン株式会社 | ハニカム構造体及びその製造方法 |
CN100462126C (zh) * | 2004-05-18 | 2009-02-18 | 揖斐电株式会社 | 蜂窝结构体及废气净化装置 |
WO2006025498A1 (ja) * | 2004-09-02 | 2006-03-09 | Ibiden Co., Ltd. | ハニカム構造体、その製造方法及び排気浄化装置 |
EP1795261A4 (en) * | 2004-09-30 | 2009-07-08 | Ibiden Co Ltd | ALVEOLAR STRUCTURE |
ATE456397T1 (de) | 2004-09-30 | 2010-02-15 | Ibiden Co Ltd | Wabenstruktur |
WO2006041174A1 (ja) * | 2004-10-12 | 2006-04-20 | Ibiden Co., Ltd. | セラミックハニカム構造体 |
EP1818098A4 (en) * | 2004-11-26 | 2008-02-06 | Ibiden Co Ltd | hONEYCOMB STRUCTURE |
JP4880581B2 (ja) * | 2005-02-04 | 2012-02-22 | イビデン株式会社 | セラミックハニカム構造体 |
JP4870657B2 (ja) * | 2005-02-04 | 2012-02-08 | イビデン株式会社 | セラミックハニカム構造体およびその製造方法 |
JP4812316B2 (ja) * | 2005-03-16 | 2011-11-09 | イビデン株式会社 | ハニカム構造体 |
JP4870559B2 (ja) | 2005-03-28 | 2012-02-08 | イビデン株式会社 | ハニカム構造体 |
CN101146742B (zh) * | 2005-03-30 | 2013-05-01 | 揖斐电株式会社 | 含碳化硅颗粒、制造碳化硅质烧结体的方法、碳化硅质烧结体以及过滤器 |
WO2006117899A1 (ja) * | 2005-04-28 | 2006-11-09 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2006132011A1 (ja) * | 2005-06-06 | 2006-12-14 | Ibiden Co., Ltd. | 梱包材及びハニカム構造体の輸送方法 |
WO2007000847A1 (ja) * | 2005-06-29 | 2007-01-04 | Ibiden Co., Ltd. | ハニカム構造体 |
EP1832565A4 (en) * | 2005-08-03 | 2007-10-17 | Ibiden Co Ltd | TEMPLATE FOR COOKING SILICON CARBIDE AND PROCESS FOR PRODUCING POROUS SILICON CARBIDE BODY |
CN100540111C (zh) * | 2005-08-26 | 2009-09-16 | 揖斐电株式会社 | 蜂窝结构体及其制造方法 |
JP5209315B2 (ja) * | 2005-09-28 | 2013-06-12 | イビデン株式会社 | ハニカムフィルタ |
WO2007039991A1 (ja) * | 2005-10-05 | 2007-04-12 | Ibiden Co., Ltd. | 押出成形用金型及び多孔質セラミック部材の製造方法 |
JPWO2007043245A1 (ja) * | 2005-10-12 | 2009-04-16 | イビデン株式会社 | ハニカムユニット及びハニカム構造体 |
KR100738131B1 (ko) * | 2005-11-10 | 2007-07-10 | 현대자동차주식회사 | 디젤매연촉매여과필터의 촉매 코팅 방법 |
CN100560180C (zh) * | 2005-11-18 | 2009-11-18 | 揖斐电株式会社 | 蜂窝结构体 |
CN101312809A (zh) * | 2005-12-26 | 2008-11-26 | 揖斐电株式会社 | 蜂窝结构体的制造方法 |
WO2007074528A1 (ja) * | 2005-12-27 | 2007-07-05 | Ibiden Co., Ltd. | 脱脂用治具、セラミック成形体の脱脂方法、及び、ハニカム構造体の製造方法 |
WO2007086183A1 (ja) * | 2006-01-27 | 2007-08-02 | Ibiden Co., Ltd. | ハニカム構造体及びその製造方法 |
WO2007086143A1 (ja) * | 2006-01-30 | 2007-08-02 | Ibiden Co., Ltd. | ハニカム構造体の検査方法、及び、ハニカム構造体の製造方法 |
JP5042505B2 (ja) * | 2006-02-07 | 2012-10-03 | 日本碍子株式会社 | 目封止ハニカム構造体 |
WO2007094075A1 (ja) * | 2006-02-17 | 2007-08-23 | Ibiden Co., Ltd. | 乾燥用治具組立装置、乾燥用治具分解装置、乾燥用治具循環装置、セラミック成形体の乾燥方法、及び、ハニカム構造体の製造方法 |
WO2007097000A1 (ja) * | 2006-02-24 | 2007-08-30 | Ibiden Co., Ltd. | ハニカム成形体用封口装置、封止材ペーストの充填方法、及び、ハニカム構造体の製造方法 |
WO2007096986A1 (ja) | 2006-02-24 | 2007-08-30 | Ibiden Co., Ltd. | 端面加熱装置、ハニカム集合体の端面乾燥方法、及び、ハニカム構造体の製造方法 |
WO2007097004A1 (ja) * | 2006-02-24 | 2007-08-30 | Ibiden Co., Ltd. | 湿式混合機、湿式混合方法及びハニカム構造体の製造方法 |
PL1826517T3 (pl) * | 2006-02-28 | 2009-01-30 | Ibiden Co Ltd | Suszący przyrząd obróbkowy, sposób suszenia wytłoczonego korpusu o strukturze plastra miodu oraz sposób wytwarzania formowanego korpusu o strukturze plastra miodu |
WO2007102216A1 (ja) * | 2006-03-08 | 2007-09-13 | Ibiden Co., Ltd. | 脱脂炉投入装置、及び、ハニカム構造体の製造方法 |
WO2007102217A1 (ja) * | 2006-03-08 | 2007-09-13 | Ibiden Co., Ltd. | 焼成体用冷却機、焼成炉、セラミック焼成体の冷却方法、及び、ハニカム構造体の製造方法 |
WO2007108076A1 (ja) * | 2006-03-17 | 2007-09-27 | Ibiden Co., Ltd. | 乾燥装置、セラミック成形体の乾燥方法及びハニカム構造体の製造方法 |
EP2008985B1 (en) | 2006-03-30 | 2015-06-24 | NGK Insulators, Ltd. | Bonded element and honeycomb sutructure using the same |
WO2007116529A1 (ja) * | 2006-04-11 | 2007-10-18 | Ibiden Co., Ltd. | 成形体切断装置、セラミック成形体の切断方法、及び、ハニカム構造体の製造方法 |
WO2007122680A1 (ja) * | 2006-04-13 | 2007-11-01 | Ibiden Co., Ltd. | 押出成形機、押出成形方法及びハニカム構造体の製造方法 |
WO2007122707A1 (ja) * | 2006-04-19 | 2007-11-01 | Ibiden Co., Ltd. | ハニカム構造体の製造方法 |
WO2007122716A1 (ja) * | 2006-04-20 | 2007-11-01 | Ibiden Co., Ltd. | 搬送装置、及び、ハニカム構造体の製造方法 |
WO2007122715A1 (ja) * | 2006-04-20 | 2007-11-01 | Ibiden Co., Ltd. | ハニカム焼成体の検査方法、及び、ハニカム構造体の製造方法 |
WO2007129391A1 (ja) * | 2006-05-01 | 2007-11-15 | Ibiden Co., Ltd. | 焼成用治具組立装置、焼成用治具分解装置、循環装置、セラミック成形体の焼成方法、及び、ハニカム構造体の製造方法 |
WO2007129399A1 (ja) * | 2006-05-08 | 2007-11-15 | Ibiden Co., Ltd. | ハニカム構造体の製造方法、ハニカム成形体受取機及びハニカム成形体取出機 |
WO2007132530A1 (ja) * | 2006-05-17 | 2007-11-22 | Ibiden Co., Ltd. | ハニカム成形体用端面処理装置、ハニカム成形体の封止方法、及び、ハニカム構造体の製造方法 |
WO2007138701A1 (ja) * | 2006-05-31 | 2007-12-06 | Ibiden Co., Ltd. | 把持装置、及び、ハニカム構造体の製造方法 |
DE602006005804D1 (de) * | 2006-07-07 | 2009-04-30 | Ibiden Co Ltd | Apparat und Verfahren zur Bearbeitung der Endfläche eines Wabenkörpers und Verfahren zur Herstellung eines Wabenkörpers |
DE102006041979A1 (de) * | 2006-09-07 | 2008-03-27 | Robert Bosch Gmbh | Filterelement, insbesondere zur Filterung von Abgasen einer Brennkraftmaschine |
WO2008032391A1 (fr) * | 2006-09-14 | 2008-03-20 | Ibiden Co., Ltd. | Procédé de production d'une structure en nid d'abeille et composition de matière première pour nid d'abeille calciné |
WO2008032390A1 (fr) * | 2006-09-14 | 2008-03-20 | Ibiden Co., Ltd. | Procédé de production d'une structure en nid d'abeille |
PL1900709T3 (pl) * | 2006-09-14 | 2010-11-30 | Ibiden Co Ltd | Sposób wytwarzania korpusu o strukturze plastra miodu i kompozycja materiałowa do wypalanego korpusu o strukturze plastra miodu |
WO2008047404A1 (fr) * | 2006-10-16 | 2008-04-24 | Ibiden Co., Ltd. | Support de montage pour structure alvéolaire et dispositif d'inspection pour structure alvéolaire |
US8092624B2 (en) * | 2006-12-07 | 2012-01-10 | Ngk Insulators, Ltd. | Bonding material composition and method for manufacturing the same, and joined body and method for manufacturing the same |
EP1939261B1 (en) * | 2006-12-25 | 2010-03-31 | Ngk Insulators, Ltd. | Joined body and method for manufacturing the same |
JP4853291B2 (ja) * | 2007-01-10 | 2012-01-11 | 日産自動車株式会社 | 排気ガス浄化触媒及びその製造方法 |
JP5084517B2 (ja) * | 2007-01-26 | 2012-11-28 | イビデン株式会社 | 外周層形成装置 |
US8158195B2 (en) | 2007-02-09 | 2012-04-17 | Nissan Motor Co., Ltd. | Catalytic converter and manufacturing method thereof |
WO2008105081A1 (ja) * | 2007-02-28 | 2008-09-04 | Ibiden Co., Ltd. | ハニカムフィルタ |
WO2008105082A1 (ja) * | 2007-02-28 | 2008-09-04 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2008120291A1 (ja) * | 2007-02-28 | 2008-10-09 | Ibiden Co., Ltd. | ハニカム構造体の製造方法 |
CN101421016B (zh) * | 2007-03-30 | 2012-04-25 | 揖斐电株式会社 | 蜂窝结构体和蜂窝结构体的制造方法 |
WO2008126321A1 (ja) * | 2007-03-30 | 2008-10-23 | Ibiden Co., Ltd. | 排ガス浄化システム |
WO2008126334A1 (ja) * | 2007-03-30 | 2008-10-23 | Ibiden Co., Ltd. | ハニカム構造体の製造方法 |
WO2008126331A1 (ja) * | 2007-03-30 | 2008-10-23 | Ibiden Co., Ltd. | ハニカムフィルタ |
WO2008126332A1 (ja) | 2007-03-30 | 2008-10-23 | Ibiden Co., Ltd. | ハニカムフィルタ |
WO2008126330A1 (ja) * | 2007-03-30 | 2008-10-23 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2008126333A1 (ja) * | 2007-03-30 | 2008-10-23 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2008126320A1 (ja) * | 2007-03-30 | 2008-10-23 | Ibiden Co., Ltd. | ハニカム構造体の製造方法 |
WO2008136078A1 (ja) * | 2007-04-20 | 2008-11-13 | Ibiden Co., Ltd. | ハニカムフィルタ |
WO2008139581A1 (ja) * | 2007-05-09 | 2008-11-20 | Ibiden Co., Ltd. | 炭化ケイ素焼成用原料の製造方法、及び、ハニカム構造体の製造方法 |
WO2008139608A1 (ja) * | 2007-05-14 | 2008-11-20 | Ibiden Co., Ltd. | ハニカム構造体及び該ハニカム構造体の製造方法 |
FR2916656B1 (fr) * | 2007-05-30 | 2011-05-13 | Peugeot Citroen Automobiles Sa | Monolithe catalytique pour gaz d'echappement issus d'un moteur a combustion interne |
WO2008149435A1 (ja) * | 2007-06-06 | 2008-12-11 | Ibiden Co., Ltd. | 焼成用治具及びハニカム構造体の製造方法 |
WO2008155856A1 (ja) | 2007-06-21 | 2008-12-24 | Ibiden Co., Ltd. | ハニカム構造体、及び、ハニカム構造体の製造方法 |
EP2017003A1 (en) * | 2007-07-20 | 2009-01-21 | Pall Corporation | Catalytic element |
WO2009020835A2 (en) * | 2007-08-03 | 2009-02-12 | Errcive, Inc. | Porous bodies and methods |
JP5180835B2 (ja) * | 2007-10-31 | 2013-04-10 | イビデン株式会社 | ハニカム構造体用梱包体、及び、ハニカム構造体の輸送方法 |
WO2009066388A1 (ja) * | 2007-11-21 | 2009-05-28 | Ibiden Co., Ltd. | ハニカム構造体及びハニカム構造体の製造方法 |
WO2009101683A1 (ja) | 2008-02-13 | 2009-08-20 | Ibiden Co., Ltd. | ハニカム構造体の製造方法 |
WO2009101682A1 (ja) * | 2008-02-13 | 2009-08-20 | Ibiden Co., Ltd. | ハニカム構造体、排ガス浄化装置、及び、ハニカム構造体の製造方法 |
WO2009107230A1 (ja) * | 2008-02-29 | 2009-09-03 | イビデン株式会社 | ハニカム構造体用シール材、ハニカム構造体、及び、ハニカム構造体の製造方法 |
WO2009118814A1 (ja) * | 2008-03-24 | 2009-10-01 | イビデン株式会社 | ハニカムフィルタ |
WO2009118813A1 (ja) * | 2008-03-24 | 2009-10-01 | イビデン株式会社 | ハニカム構造体及びハニカム構造体の製造方法 |
WO2009118862A1 (ja) * | 2008-03-27 | 2009-10-01 | イビデン株式会社 | ハニカム構造体の製造方法 |
JP5604046B2 (ja) | 2008-03-28 | 2014-10-08 | 日本碍子株式会社 | ハニカム構造体 |
WO2011100527A1 (en) * | 2010-02-12 | 2011-08-18 | Morgan Advanced Ceramics, Inc. | Method for texturing ceramic components |
JP5808619B2 (ja) | 2011-09-06 | 2015-11-10 | 日本碍子株式会社 | ハニカム構造体、及びハニカム触媒体 |
KR101217169B1 (ko) | 2012-03-07 | 2012-12-31 | 아이앤비에어 주식회사 | 허니컴 구조의 세라믹 바이오 필터 및 그의 제조 방법 |
JP6200212B2 (ja) * | 2012-12-03 | 2017-09-20 | 日本碍子株式会社 | ハニカム触媒体 |
JP6231908B2 (ja) * | 2014-03-14 | 2017-11-15 | 日本碍子株式会社 | 目封止ハニカム構造体 |
JP6081951B2 (ja) * | 2014-03-26 | 2017-02-15 | 日本碍子株式会社 | ハニカム構造体の製造方法 |
JP2016142484A (ja) * | 2015-02-03 | 2016-08-08 | イビデン株式会社 | 準カプセル溶融塩蓄熱材 |
KR102628229B1 (ko) | 2015-11-20 | 2024-01-22 | 1934612 온타리오 인코포레이티드 | 실리콘 탄화물 멤브레인으로 유체를 정화하기 위한 장치, 시스템 및 방법 |
CN114700118B (zh) * | 2016-12-12 | 2024-05-07 | 康明泰克股份有限公司 | Scr催化剂模块及其对应的催化剂反应器 |
JP6788515B2 (ja) * | 2017-02-02 | 2020-11-25 | 日本碍子株式会社 | 目封止ハニカム構造体 |
JP6982530B2 (ja) * | 2018-03-23 | 2021-12-17 | 日本碍子株式会社 | ハニカム構造体 |
CN114471151A (zh) * | 2018-07-18 | 2022-05-13 | 深圳大学 | 催化炉 |
SG11202110059PA (en) * | 2019-03-28 | 2021-10-28 | Mitsubishi Chem Corp | Molded catalyst body, and method for producing unsaturated aldehyde and unsaturated carboxylic acid using same |
WO2021049094A1 (ja) * | 2019-09-11 | 2021-03-18 | 日本碍子株式会社 | ハニカム構造体及び排気ガス浄化装置 |
JP7274395B2 (ja) * | 2019-10-11 | 2023-05-16 | 日本碍子株式会社 | ハニカム構造体 |
JP7353218B2 (ja) * | 2020-03-02 | 2023-09-29 | 日本碍子株式会社 | ハニカムフィルタ |
JP7449721B2 (ja) * | 2020-03-02 | 2024-03-14 | 日本碍子株式会社 | ハニカムフィルタ |
JP7234180B2 (ja) * | 2020-03-31 | 2023-03-07 | 日本碍子株式会社 | セラミックス製のフィルタ |
JP2022142543A (ja) * | 2021-03-16 | 2022-09-30 | 日本碍子株式会社 | ハニカム構造体及び電気加熱式担体 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000279729A (ja) * | 1999-03-30 | 2000-10-10 | Ibiden Co Ltd | セラミックフィルタユニット及びその製造方法、セラミックフィルタ |
JP2001199777A (ja) * | 2000-01-17 | 2001-07-24 | Ngk Insulators Ltd | ハニカム構造体及びその製造方法 |
JP2001269585A (ja) * | 2000-03-24 | 2001-10-02 | Ngk Insulators Ltd | 排ガス浄化用フィルター |
JP2002201082A (ja) * | 2000-04-14 | 2002-07-16 | Ngk Insulators Ltd | ハニカム構造体及びその製造方法 |
JP2002234779A (ja) * | 2001-02-02 | 2002-08-23 | Ngk Insulators Ltd | ハニカム構造体及びその製造方法 |
JP2003001029A (ja) * | 2001-06-18 | 2003-01-07 | Hitachi Metals Ltd | 多孔質セラミックハニカムフィルタ |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3071105A (en) * | 1959-08-26 | 1963-01-01 | Stewart Warner Corp | Electroluminescent gauge |
US3093657A (en) * | 1960-01-14 | 1963-06-11 | Hoechst Ag | Process of preparing nitro-3-hydroxy-thiophene-2-carboxylic acid esters |
JPS6065219A (ja) * | 1983-09-20 | 1985-04-15 | Nissan Motor Co Ltd | 内燃機関のパ−テイキユレ−トトラツプ |
JP3272746B2 (ja) | 1991-07-19 | 2002-04-08 | イビデン株式会社 | ディーゼルパティキュレートフィルタ |
JP2726616B2 (ja) * | 1993-12-15 | 1998-03-11 | 日本碍子株式会社 | 多孔質セラミックハニカムフィルタ |
JP4246802B2 (ja) * | 1995-08-22 | 2009-04-02 | 東京窯業株式会社 | ハニカム構造体とその製造方法及び用途、並びに加熱装置 |
EP0761279B1 (en) * | 1995-08-22 | 2002-11-20 | Denki Kagaku Kogyo Kabushiki Kaisha | Honeycomb structure |
DE69630681T2 (de) * | 1996-01-12 | 2004-04-22 | Ibiden Co. Ltd., Ogaki | Keramische struktur |
US5930994A (en) * | 1996-07-02 | 1999-08-03 | Ibiden Co., Ltd. | Reverse cleaning regeneration type exhaust emission control device and method of regenerating the same |
JP2000167329A (ja) * | 1998-09-30 | 2000-06-20 | Ibiden Co Ltd | 排気ガス浄化装置の再生システム |
JP2002530175A (ja) | 1998-11-20 | 2002-09-17 | コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ | コードレス走査ヘッドの充電器を備える超音波診断イメージングシステム |
DE60032392T2 (de) * | 1999-09-29 | 2007-10-11 | Ibiden Co., Ltd., Ogaki | Wabenförmiger Filter und Anordnung von keramischen Filtern |
JP2001329830A (ja) * | 2000-03-15 | 2001-11-30 | Ibiden Co Ltd | 排気ガス浄化フィルタの再生装置及びフィルタ再生方法、排気ガス浄化フィルタの再生プログラム及びそのプログラムを格納する記録媒体 |
JP2001269522A (ja) | 2000-03-27 | 2001-10-02 | Ngk Insulators Ltd | 多孔質セラミックス焼結体製フィルター |
WO2003071105A1 (fr) | 2000-08-24 | 2003-08-28 | Ibiden Co., Ltd. | Dispositif de controle d'emission de gaz d'echappement et structure de logement du dispositif de controle |
KR100507048B1 (ko) * | 2001-03-22 | 2005-08-05 | 이비덴 가부시키가이샤 | 배기가스 정화장치 |
JP4511071B2 (ja) * | 2001-03-29 | 2010-07-28 | 日本碍子株式会社 | ハニカム構造体及びそのアッセンブリ |
EP1403231B1 (en) * | 2001-05-31 | 2012-11-21 | Ibiden Co., Ltd. | Method of producing a porous ceramic sintered body |
US6827754B2 (en) * | 2001-09-13 | 2004-12-07 | Hitachi Metals, Ltd. | Ceramic honeycomb filter |
US7648547B2 (en) | 2002-04-10 | 2010-01-19 | Ibiden Co., Ltd. | Honeycomb filter for clarifying exhaust gas |
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CN100462126C (zh) | 2004-05-18 | 2009-02-18 | 揖斐电株式会社 | 蜂窝结构体及废气净化装置 |
EP1795261A4 (en) | 2004-09-30 | 2009-07-08 | Ibiden Co Ltd | ALVEOLAR STRUCTURE |
ATE456397T1 (de) | 2004-09-30 | 2010-02-15 | Ibiden Co Ltd | Wabenstruktur |
WO2006041174A1 (ja) | 2004-10-12 | 2006-04-20 | Ibiden Co., Ltd. | セラミックハニカム構造体 |
EP1818098A4 (en) | 2004-11-26 | 2008-02-06 | Ibiden Co Ltd | hONEYCOMB STRUCTURE |
EP1707251B1 (en) | 2004-12-28 | 2012-10-10 | Ibiden Co., Ltd. | Filter and filter aggregate |
JP4880581B2 (ja) | 2005-02-04 | 2012-02-22 | イビデン株式会社 | セラミックハニカム構造体 |
JP4870657B2 (ja) | 2005-02-04 | 2012-02-08 | イビデン株式会社 | セラミックハニカム構造体およびその製造方法 |
JP2006223983A (ja) | 2005-02-17 | 2006-08-31 | Ibiden Co Ltd | ハニカム構造体 |
JP4812316B2 (ja) | 2005-03-16 | 2011-11-09 | イビデン株式会社 | ハニカム構造体 |
JP4870559B2 (ja) | 2005-03-28 | 2012-02-08 | イビデン株式会社 | ハニカム構造体 |
KR100810476B1 (ko) | 2005-03-28 | 2008-03-07 | 이비덴 가부시키가이샤 | 허니컴 구조체 |
CN101146742B (zh) | 2005-03-30 | 2013-05-01 | 揖斐电株式会社 | 含碳化硅颗粒、制造碳化硅质烧结体的方法、碳化硅质烧结体以及过滤器 |
CN1926313B (zh) | 2005-04-07 | 2011-12-28 | 揖斐电株式会社 | 蜂窝状结构体 |
JP2006289237A (ja) | 2005-04-08 | 2006-10-26 | Ibiden Co Ltd | ハニカム構造体 |
CN1954137B (zh) | 2005-07-21 | 2011-12-21 | 揖斐电株式会社 | 蜂窝结构体以及废气净化装置 |
CN100540111C (zh) | 2005-08-26 | 2009-09-16 | 揖斐电株式会社 | 蜂窝结构体及其制造方法 |
JP5209315B2 (ja) | 2005-09-28 | 2013-06-12 | イビデン株式会社 | ハニカムフィルタ |
CN101061293B (zh) | 2005-11-18 | 2011-12-21 | 揖斐电株式会社 | 蜂窝结构体 |
CN100560180C (zh) | 2005-11-18 | 2009-11-18 | 揖斐电株式会社 | 蜂窝结构体 |
WO2007086183A1 (ja) | 2006-01-27 | 2007-08-02 | Ibiden Co., Ltd. | ハニカム構造体及びその製造方法 |
WO2007097056A1 (ja) | 2006-02-23 | 2007-08-30 | Ibiden Co., Ltd. | ハニカム構造体および排ガス浄化装置 |
JP4863904B2 (ja) | 2006-03-31 | 2012-01-25 | イビデン株式会社 | ハニカム構造体およびその製造方法 |
-
2004
- 2004-02-27 US US10/527,531 patent/US7504359B2/en active Active
- 2004-02-27 WO PCT/JP2004/002373 patent/WO2004076027A1/ja active Application Filing
- 2004-02-27 JP JP2005502950A patent/JP4516017B2/ja not_active Expired - Lifetime
- 2004-02-27 KR KR1020057008442A patent/KR100632161B1/ko active IP Right Grant
- 2004-02-27 AT AT04715472T patent/ATE481151T1/de not_active IP Right Cessation
- 2004-02-27 EP EP04715472A patent/EP1598102B1/en not_active Expired - Lifetime
- 2004-02-27 CN CNB200480001416XA patent/CN1326593C/zh not_active Expired - Lifetime
- 2004-02-27 DE DE602004029140T patent/DE602004029140D1/de not_active Expired - Lifetime
-
2010
- 2010-02-03 JP JP2010021945A patent/JP2010156343A/ja active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000279729A (ja) * | 1999-03-30 | 2000-10-10 | Ibiden Co Ltd | セラミックフィルタユニット及びその製造方法、セラミックフィルタ |
JP2001199777A (ja) * | 2000-01-17 | 2001-07-24 | Ngk Insulators Ltd | ハニカム構造体及びその製造方法 |
JP2001269585A (ja) * | 2000-03-24 | 2001-10-02 | Ngk Insulators Ltd | 排ガス浄化用フィルター |
JP2002201082A (ja) * | 2000-04-14 | 2002-07-16 | Ngk Insulators Ltd | ハニカム構造体及びその製造方法 |
JP2002234779A (ja) * | 2001-02-02 | 2002-08-23 | Ngk Insulators Ltd | ハニカム構造体及びその製造方法 |
JP2003001029A (ja) * | 2001-06-18 | 2003-01-07 | Hitachi Metals Ltd | 多孔質セラミックハニカムフィルタ |
Cited By (36)
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US7387657B2 (en) | 2002-10-07 | 2008-06-17 | Ibiden Co., Ltd. | Honeycomb structural body |
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Also Published As
Publication number | Publication date |
---|---|
JPWO2004076027A1 (ja) | 2006-06-01 |
ATE481151T1 (de) | 2010-10-15 |
EP1598102A1 (en) | 2005-11-23 |
CN1326593C (zh) | 2007-07-18 |
DE602004029140D1 (de) | 2010-10-28 |
JP2010156343A (ja) | 2010-07-15 |
KR20050074994A (ko) | 2005-07-19 |
EP1598102B1 (en) | 2010-09-15 |
KR100632161B1 (ko) | 2006-10-11 |
EP1598102A4 (en) | 2006-07-05 |
JP4516017B2 (ja) | 2010-08-04 |
CN1705502A (zh) | 2005-12-07 |
US20060166820A1 (en) | 2006-07-27 |
US7504359B2 (en) | 2009-03-17 |
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