WO2005044422A1 - ハニカム構造体 - Google Patents
ハニカム構造体 Download PDFInfo
- Publication number
- WO2005044422A1 WO2005044422A1 PCT/JP2004/016442 JP2004016442W WO2005044422A1 WO 2005044422 A1 WO2005044422 A1 WO 2005044422A1 JP 2004016442 W JP2004016442 W JP 2004016442W WO 2005044422 A1 WO2005044422 A1 WO 2005044422A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- honeycomb structure
- catalyst
- wall
- porous ceramic
- material layer
- Prior art date
Links
- 239000000919 ceramic Substances 0.000 claims abstract description 176
- 239000003054 catalyst Substances 0.000 claims abstract description 164
- 239000002245 particle Substances 0.000 claims abstract description 37
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 20
- 239000010703 silicon Substances 0.000 claims abstract description 19
- 239000002131 composite material Substances 0.000 claims abstract description 10
- 239000003566 sealing material Substances 0.000 claims description 66
- 238000005192 partition Methods 0.000 claims description 29
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 8
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 7
- 239000010410 layer Substances 0.000 description 89
- 238000000034 method Methods 0.000 description 83
- 239000007789 gas Substances 0.000 description 63
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 56
- 239000000463 material Substances 0.000 description 53
- 210000004027 cell Anatomy 0.000 description 31
- 238000011069 regeneration method Methods 0.000 description 31
- 230000000052 comparative effect Effects 0.000 description 28
- 229910052697 platinum Inorganic materials 0.000 description 28
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 26
- 230000008929 regeneration Effects 0.000 description 25
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 21
- 239000011230 binding agent Substances 0.000 description 17
- 238000011068 loading method Methods 0.000 description 14
- 230000001172 regenerating effect Effects 0.000 description 13
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
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- 239000000126 substance Substances 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910010293 ceramic material Inorganic materials 0.000 description 3
- 229910003460 diamond Inorganic materials 0.000 description 3
- 239000010432 diamond Substances 0.000 description 3
- 229920000609 methyl cellulose Polymers 0.000 description 3
- 239000001923 methylcellulose Substances 0.000 description 3
- 235000010981 methylcellulose Nutrition 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 150000002926 oxygen Chemical class 0.000 description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
- 229910052582 BN Inorganic materials 0.000 description 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
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- 238000000576 coating method Methods 0.000 description 2
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- 238000007872 degassing Methods 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 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 2
- 230000000694 effects Effects 0.000 description 2
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- 239000000945 filler Substances 0.000 description 2
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- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229910052863 mullite Inorganic materials 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 238000003980 solgel method Methods 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- MIDXCONKKJTLDX-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-dione Chemical compound CC1CC(C)C(=O)C1=O MIDXCONKKJTLDX-UHFFFAOYSA-N 0.000 description 1
- 238000007088 Archimedes method Methods 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229910052777 Praseodymium Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 229910026551 ZrC Inorganic materials 0.000 description 1
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
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- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000013736 caramel Nutrition 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 229910052878 cordierite Inorganic materials 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 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
- 150000002009 diols Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
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- 239000003822 epoxy resin Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
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- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- -1 methanol Chemical compound 0.000 description 1
- NFFIWVVINABMKP-UHFFFAOYSA-N methylidynetantalum Chemical compound [Ta]#C NFFIWVVINABMKP-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910003468 tantalcarbide Inorganic materials 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 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 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
- 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
- B01D46/24491—Porosity
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
- 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
- B01D46/24492—Pore diameter
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
- 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
- B01D46/2451—Honeycomb filters characterized by the geometrical structure, shape, pattern or configuration or parameters related to the geometry of the structure
- B01D46/2455—Honeycomb filters characterized by the geometrical structure, shape, pattern or configuration or parameters related to the geometry of the structure of the whole honeycomb or segments
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
- 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
- B01D46/2451—Honeycomb filters characterized by the geometrical structure, shape, pattern or configuration or parameters related to the geometry of the structure
- B01D46/2476—Monolithic structures
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
- 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
- B01D46/2451—Honeycomb filters characterized by the geometrical structure, shape, pattern or configuration or parameters related to the geometry of the structure
- B01D46/2478—Structures comprising honeycomb segments
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
- 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
- B01D46/2451—Honeycomb filters characterized by the geometrical structure, shape, pattern or configuration or parameters related to the geometry of the structure
- B01D46/2484—Cell density, area or aspect ratio
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
- 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
- B01D46/2498—The honeycomb filter being defined by mathematical relationships
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00793—Uses not provided for elsewhere in C04B2111/00 as filters or diaphragms
Definitions
- the present invention relates to a honeycomb structure used as a filter or the like for removing particulates and the like in exhaust gas discharged from an internal combustion engine such as a diesel engine.
- exhaust gas used in many private automobiles and the like which also discharges gasoline engine power, usually contains HC, CO, NOx, and the like.
- An exhaust gas purification system has been developed in which a catalyst carrier carrying a source catalyst is disposed in an exhaust gas passage.
- FIG. 6 is a cross-sectional perspective view schematically showing a catalyst carrier used in such an exhaust gas purification system.
- the catalyst carrier 70 is a honeycomb structure made of a porous ceramic in which a large number of through holes 71 are juxtaposed in the longitudinal direction via a wall 73. The original catalyst is supported.
- the three-way catalyst shows a high purification ratio of HC, CO, NOx, etc. in the exhaust gas only when the air-fuel ratio of the air-fuel mixture sucked into the gasoline engine is in a narrow range near the stoichiometric air-fuel ratio. Therefore, the air-fuel ratio of the air-fuel mixture sucked into the gasoline engine is controlled to be the stoichiometric air-fuel ratio.
- diesel engines used for many large-sized transportation means such as buses and trucks have a higher temperature and a leaner fuel (excessive oxygen) than the gasoline engines described above. Because of the combustion in the state, the HC and CO content in the exhaust gas is lower than that of the exhaust gas with gasoline engine power, but it has a higher NOx content and is contained in light oil as fuel. It also includes SOx caused by sulfur contained. In addition, it is a big problem that a large amount of particulate matter (particulates) is contained.
- Fig. 7 is a partially cutaway perspective view schematically showing a honeycomb structure (hardcam filter) for collecting particulates contained in exhaust gas discharged from a diesel engine. .
- the honeycomb filter 80 has a honeycomb structure composed of porous ceramics in which a large number of through holes 81 are arranged in a longitudinal direction via a wall portion 83. Either the end on the side or the exit side is sealed with a sealing material 84 so as to form a so-called checkered pattern, and the exhaust gas flowing into one through-hole 81 must be a wall separating the through-hole 81. After passing through the part 83, it flows out from the other through-holes 81. When the exhaust gas passes through the wall 83, the particulates are captured by the wall 83, and the exhaust gas is purified. You.
- Such a camfinoleta is used to collect or reduce the above-mentioned HC, CO, NOx, etc. contained in the above-mentioned exhaust gas together with the collection of the particulates in the above-mentioned exhaust gas.
- a catalyst for removing substances is supported.
- honeycomb filter if a certain amount or more of particulates on the wall of the above-mentioned honeycomb filter is trapped, the pressure drop becomes so high that it cannot be used, so that the trapped particulates are removed by thermal decomposition. It is necessary to perform a regeneration process for regenerating the honeycomb filter.
- the burning temperature of particulates is about 550-630 ° C.
- a catalyst that oxidizes and removes the particulates is carried on the wall of the honeycomb filter, the particulates burn due to the catalytic action. The temperature can be reduced.
- honeycomb filter supporting such a catalyst for example, cordierite or the like is formed on the surface of a filtration wall (cell wall) of a heat-resistant carrier formed like a nod-cam filter shown in FIG. , ⁇ -alumina carrier layer is formed, and noble metal such as Pt, Pd, Rh Carriers carrying a catalytically active component such as caramel are well known (hereinafter, also referred to as supporting method (1)).
- a fine powder obtained by adding an inorganic binder to ⁇ -alumina, mixing and pulverizing the slurry is used as a slurry, and the slurry is uniformly sprayed on the wall surface of the cordierite-noc-cam carrier to cover the same.
- an alumina layer is formed by so-called push coating (for example, see Patent Document 1).
- the above-mentioned push-coated alumina layer fills the pores of the wall surface of the cordierite-nod-cam carrier, and the above-mentioned alumina layer has a small pore diameter and a small porosity, and has a low resistance to ventilation. Because of its large size, there has been a problem that the pressure loss is significantly higher than that of a honeycomb carrier having no alumina layer.
- the technology (supporting method (2)) developed earlier by the present inventors is that the pores that cannot block the gaps generated between the particles constituting the porous ceramic carrier are maintained as pores.
- the filter had a smaller pressure loss than that of the above-mentioned loading method (1).
- Patent Document 1 Japanese Patent Application Laid-Open No. 05-68892
- Patent Document 2 JP 2001-137714 A
- the inventors of the present invention have conducted further intensive studies in order to obtain a honeycomb filter for exhaust gas purification which is excellent in the regeneration efficiency of collected particulates.
- the opening ratio and the amount of catalyst carried in the honeycomb structure that constitutes the honeycomb filter for conversion are set to fixed values, and this does not necessarily result in a honeycomb filter with excellent regeneration efficiency. There was found.
- the regeneration rate of the collected particulate matter is closely related to the opening ratio of the exhaust gas purification honeycomb filter and the amount of the catalyst carried thereon, and Paying attention to the fact that silicon is deeply involved in a catalyst for purifying exhaust gas, the opening ratio of the above-mentioned cam-cam filter and the amount of the supported catalyst are set within predetermined ranges, and the composite is formed using silicon. It has been found that the configuration of (1) can improve the regeneration rate of the honeycomb filter, and have completed the present invention.
- a column-shaped porous ceramic member in which a large number of through-holes are juxtaposed in the longitudinal direction across a partition wall, and one end of one of the through-holes is sealed.
- a honeycomb structure composed of two or more,
- the porous ceramic member is a composite comprising ceramic particles and silicon, and a catalyst is supported on the wall portion.
- An aperture ratio ⁇ (%) of the honeycomb structure and a supported amount (gZL) of the catalyst have a relationship represented by the following formula (1).
- the opening ratio ⁇ (%) of the honeycomb structure and the supported amount of catalyst i8 (gZL) have the relationship of the above formula (1). This means that the catalyst necessary for oxidizing and removing the particulate matter accumulated on the wall is sufficiently supported, and therefore, the regeneration treatment of the honeycomb structure is performed. If you do, the regeneration rate will be very good.
- a column-shaped porous ceramic member having a large number of through-holes arranged in the longitudinal direction across a partition wall, and one end of one of these through-holes sealed. Or a honeycomb structure composed of two or more,
- the porous ceramic member is a composite composed of ceramic particles and silicon, and a catalyst is supported on the wall,
- An aperture ratio ⁇ (%) of the honeycomb structure and a supported amount (gZL) of the catalyst have a relationship represented by the following formula (1).
- the "opening ratio of the honeycomb structure” refers to a cross section in a direction perpendicular to the longitudinal direction of the honeycomb structure (the direction perpendicular to the longitudinal direction of the through hole).
- a honeycomb structure used as a general filter for purifying exhaust gas (for collecting particulates) includes three types: a partition wall, a through hole, and a sealing portion. Therefore, the aperture ratio in the present invention is a ratio of the cross-sectional area of the honeycomb structure to the sum of the area of the through hole and the sealing portion (the sum of the area of the partition wall is subtracted from the cross section of the filter). .
- the sealing portions at both ends are not approximately the same amount (for example, when the number of sealing portions at both ends is changed differently, when the cross-sectional shape of the through hole is changed, etc.)
- the sealing shape is not taken into account, and is calculated by the method described above.
- the cross-sectional area of the honeycomb structure does not include a portion occupied by the sealing material layer.
- the honeycomb structure of the present invention is formed by assembling one or more columnar porous ceramic members having a large number of through-holes arranged in a longitudinal direction with a wall portion therebetween.
- the catalyst is carried on the part.
- the above-mentioned honeycomb structure is configured as an assembly in which a plurality of columnar porous ceramic members in which a plurality of through-holes are juxtaposed in the longitudinal direction across a partition wall are bound together via a sealing material layer.
- assembly-type honeycomb structure a porous ceramic member that is entirely formed as a single member may be configured.
- integrated honeycomb structure also referred to as “integrated honeycomb structure”.
- the wall is made of a porous ceramic. And a sealing material layer that functions as an adhesive layer between the outer wall of the porous ceramic member and the porous ceramic member. Functions as a filter for collecting particles. That is, a part of the wall functions as a particle collecting filter.
- the wall portion is constituted by only one type of partition wall, and the entire wall portion functions as a filter for collecting particles. .
- FIG. 1 is a perspective view schematically showing a specific example of an aggregate-type honeycomb structure which is an example of the honeycomb structure of the present invention.
- FIG. 2 (a) is a perspective view of FIG.
- FIG. 2 is a perspective view schematically showing an example of a porous ceramic member constituting the aggregated honeycomb structure shown in FIG. 1B
- FIG. 1B is a cross-sectional view taken along line AA of the porous ceramic member shown in FIG. FIG.
- a plurality of porous ceramic members 20 are bound via a sealing material layer 14 to form a ceramic block 15, Around the ceramic block 15, a sealing material layer 13 for preventing leakage of exhaust gas is formed.
- the porous ceramic member 20 has a sealing material 22 that is located at one end of the through hole 21 on the exhaust gas inlet or outlet side.
- the exhaust gas that has been plugged in and has flowed into one through-hole 21 always passes through the partition wall 23 separating the through-hole 21 and then flows out from the other through-hole 21.
- the partition walls 23 that separate each other function as a particle collection filter.
- the partition walls 23 are provided with a catalyst via a catalyst support material layer (not shown).
- FIG. 3 (a) is a perspective view schematically showing a specific example of an integrated honeycomb structure which is another example of the honeycomb structure of the present invention
- FIG. FIG. 4 is a sectional view taken along line BB of FIG.
- the integral honeycomb structure 30 also has one porous ceramic force in which a large number of through holes 31 are juxtaposed in the longitudinal direction across the wall 33. It constitutes a ceramic block 35, and the entire wall 33 is configured to function as a filter for collecting particles! RU That is, as shown in FIG. 3 (b), the through holes 31 formed in the integral honeycomb structure 30 Either the inlet side or the outlet side of the exhaust gas is sealed with a sealing material 32, and the exhaust gas flowing into one through-hole 31 must pass through the wall 33 separating the through-hole 31 and then into the other through-hole. It flows out from the through hole 31.
- the particulates contained in the exhaust gas flowing into the integral honeycomb structure 30 of the present invention are captured by the wall 33 when passing through the wall 33 so that the exhaust gas is purified. I'm familiar.
- the wall 33 is provided with a catalyst via a catalyst support material layer (not shown).
- a sealing material layer is formed around the ceramic block 35 in the same manner as the aggregated honeycomb structure 10 shown in FIG.
- the method of supporting the catalyst to be supported on the wall portion of the honeycomb structure may be any of the above-described methods (1) and (2), which are different from each other. It may be something.
- the particulate matter in the exhaust gas captured by the wall portion may be different from the case where the particulate matter is accumulated on the surface of the wall portion and the case where the particulate matter is accumulated.
- the honeycomb structure of the present invention may penetrate into the interior of the wall.
- the supporting method of the catalyst supported on the wall portion is the above-described supporting method (1)
- the particulate matter in the exhaust gas captured by the wall portion is desirably accumulated on the surface of the wall.
- the supporting method (1) is a method in which a catalyst support material layer is formed on the surface of the wall and the catalyst is supported on the catalyst support material layer, the particulates that have penetrated into the interior of the wall are oxidized by the catalyst. This is because it is difficult to make a dungeon.
- the loading method (2) is a method in which the catalyst support material layer is coated on each particle constituting the wall portion and the catalyst is loaded on the uneven surface of the catalyst support material layer. This is because the curate can be suitably oxidized.
- the method for oxidizing and purifying the particulates captured by the walls of the honeycomb structure of the present invention using a catalyst carried on the walls is not particularly limited.
- the honeycomb structure When the pressure is increased and the pressure loss of the honeycomb structure increases, the honeycomb structure is heated to a temperature at which the catalyst can function by a heating means such as a heater or a post injection to reduce the particulates.
- a heating means such as a heater or a post injection to reduce the particulates.
- active oxygen generated during the reduction of NOx in exhaust gas such as a method for purifying acid oxide (hereinafter also referred to as a regeneration method (1)) or a method such as Toyota's Diesel Particulate-NOx Reduction System (DPNR). Frequently oxidizing and purifying particulates trapped on the wall (hereinafter referred to as “regeneration method (2)”).
- the method of loading the catalyst supported on the wall is the above-described loading method (1), It is desirable to accumulate particulates only on the wall surface.
- the particulates are accumulated after a certain amount of particulates are accumulated, and when the particulates penetrate into the wall, the amount of accumulated particulates before the regeneration is performed is reduced. It becomes too much, and particulates accumulate on the wall surface.
- the regeneration process of the honeycomb structure is performed in such a state, most of the particulates to be oxidized become the particulates accumulated on the surface of the wall, and the particulates are accumulated inside the wall. This is because the accumulated particulates are hardly oxidized and purified, and substantially only the catalyst on the surface of the wall is used.
- the method for supporting the catalyst supported on the wall is the above-described supporting method (2), and the catalyst is supported even inside the wall. It is hoped that the particulates penetrate!
- the particulates accumulated inside the wall are immediately oxidized and purified, so that the catalyst supported on the inside and the surface of the wall can be used efficiently. You.
- the regeneration method (1) can be used sufficiently by changing the conditions of regeneration using the loading method (2) and oxidizing the particulates before the particulates are clogged inside the wall.
- the honeycomb structure of the present invention is a composite of ceramic particles and silicon.
- the present invention has derived an optimum range between the ratio ⁇ (%) and the supported amount of catalyst supported on the wall
- activation of gas or the like means that, for example, in a low temperature range (about 250 to 500 ° C), NOx contained in exhaust gas can be used as a gaseous activator. That is, NO in exhaust gas can be oxidized to NO with high oxidizing power. NO is very low in reducing atmosphere
- gaseous activator can promote the oxidation of particulates.
- the activated oxygen is more susceptible to particulate and low-temperature oxidation reactions than non-activated oxygen. Therefore, it is considered that the activated oxygen can promote the oxidation of the particulates.
- the opening ratio ⁇ (%) of the honeycomb structure and the supported amount of catalyst (gZL) have a relationship represented by the following formula (1).
- the required amount of supported catalyst ⁇ 8 varies depending on the opening ratio ⁇ of the honeycomb structure, and the opening ratio ⁇ of the honeycomb structure is low according to the above formula (1).
- the lower limit of the supported amount of catalyst ⁇ 8 increases, and when the opening ratio ⁇ of the honeycomb structure is high, The lower limit force of the quantity i8 is smaller.
- the opening ratio ⁇ of the honeycomb structure When the opening ratio ⁇ of the honeycomb structure is low, the ratio of the wall portion occupying the cross section perpendicular to the longitudinal direction of the honeycomb structure increases. More specifically, the aperture ratio decreases in the following cases. That is, (1) the thickness of the wall is increased. (2) Increase the number of through-holes Reduce the cross-sectional area of the through-hole.
- the opening ratio ⁇ of the honeycomb structure is high !, the ratio of the wall portion to the cross section perpendicular to the longitudinal direction of the honeycomb structure decreases. More specifically, the aperture ratio increases in the following cases. (3) Make the wall thinner. (4) Reduce the number of through holes Increase the cross-sectional area of the through holes. However, the above-mentioned conditions are not so preferable because the strength is reduced. In cases (3) and (4), in order to improve the strength, it is required to reduce the porosity of the filter and to reduce the porosity. When the porosity of the filter is reduced, particulates accumulate only on the wall surface. Since the catalyst only needs to be supported on the surface of the wall, the amount of the catalyst can be reduced.
- FIG. 4 is a graph showing the relationship between the opening ratio a (%) of the honeycomb structure and the catalyst loading j8 (gZL) in the honeycomb structure of the present invention.
- the above equation (1) shows the region above the straight line (1) shown in FIG. 4, and in the honeycomb structure of the present invention, the opening ratio / catalyst carrying amount
- the opening ratio ⁇ of the honeycomb structure is 40%
- the supported amount j8 of the catalyst is 4.8 gZL or more
- the opening ratio of the honeycomb structure is 50%
- the supported amount j8 of the catalyst is 3.55 gZL or more
- the opening ratio of the honeycomb structure is 60%
- 8 of the catalyst is 2.3 gZL or more.
- the opening ratio ⁇ (%) of the honeycomb structure and the supported amount of catalyst i8 (gZL) may have a relationship represented by the following formula (2). desirable.
- the supported amount ⁇ of the catalyst needs to satisfy the relationship of the above formula (1). If ⁇ is too large, the distance between the catalyst particles is reduced, and the sintering of the catalyst tends to occur quickly. Therefore, the aperture ratio ⁇ of the honeycomb structure and the supported amount of catalyst
- the above equation (2) shows the area below the straight line (2) shown in FIG. 4, and in the honeycomb structure of the present invention, the opening ratio ⁇ and the catalyst loading
- the supported amount j8 of the catalyst is preferably 8.OgZL or less. In the case of 50%, the supported amount of the catalyst j8 is 6.75 gZL or less. When the opening ratio of the honeycomb structure is 60%, the supported amount of the catalyst j8 is 5%. It is desirable to be less than 5gZL.
- Examples of the method of reducing the aperture ratio of the honeycomb structure include a method of increasing the thickness of the wall portion and a method of increasing the cell density.
- the pressure loss of the exhaust gas purifying apparatus using the honeycomb structure of the present invention tends to increase, and the strength tends to increase.
- the “cell density” refers to the number of through holes existing in a predetermined area (for example, 1 square inch) in a cross section perpendicular to the longitudinal direction of the honeycomb structure.
- the method for supporting the catalyst of the honeycomb structure of the present invention is the supporting method (1) and the method for regenerating the honeycomb structure is the regenerating method (1)
- the method for reducing the aperture ratio of the honeycomb structure is as follows. It is desirable to use a method for increasing the cell density. Cell of honeycomb structure of the present invention When the density is increased, the inner wall of the through-hole, that is, the area of the wall (filterable area) increases, the number of reaction sites between the particulates accumulated on the surface of the wall and the catalyst increases, and the density of the present invention increases. This is because the cam structure can be efficiently regenerated.
- the honeycomb structure of the present invention is the supporting method (2) and the method of regenerating the honeycomb structure is the regenerating method (2)
- the honeycomb structure The method of reducing the aperture ratio is preferably a method of increasing the thickness of the wall.
- the thickness of the wall of the honeycomb structure of the present invention is increased, the number of reaction sites between the particulates accumulated in the wall and the catalyst increases, and the honeycomb structure of the present invention can be efficiently regenerated. This is what you can do.
- methods for increasing the aperture ratio of the honeycomb structure include a method for reducing the thickness of the wall portion and a method for decreasing the cell density.
- the pressure loss of the exhaust gas purifying apparatus using the honeycomb structure of the present invention tends to decrease, and the strength tends to decrease.
- the method for increasing the aperture ratio of the honeycomb structure is as follows. It is preferable that the thickness of the wall be reduced. When the thickness of the wall portion of the honeycomb structure of the present invention is reduced, the inner wall of the through hole, that is, the area (filterable area) of the wall portion is increased, and the particulate matter accumulated on the surface of the wall portion is reduced. This is because the number of reaction sites with the catalyst increases, and the regeneration treatment of the honeycomb structure of the present invention can be performed efficiently.
- the method of increasing the aperture ratio is desirably the method of decreasing the cell density.
- the cell density of the honeycomb structure of the present invention is reduced, the number of reaction sites between the particulates accumulated in the wall and the catalyst increases, and the honeycomb structure of the present invention can be efficiently regenerated. It is the power that can be.
- the lower limit of the aperture ratio ⁇ of the honeycomb structure is preferably 40%. If the lower limit of the aperture ratio ⁇ is less than 40%, the pressure loss will be too high or the strength will be low. In addition, the probability of contact with silicon decreases. this At this time, the supported amount of catalyst ⁇ 8 is 4.8 gZL or more according to the above formula (1).
- a more desirable lower limit of the aperture ratio ⁇ of the honeycomb structure is 45%, and a still more desirable lower limit is 50%.
- 8 of the catalyst is 4.18 gZL or more and 3.55 gZL or more, respectively, from the above formula (1).
- the catalyst supported on the wall in the honeycomb structure of the present invention is not particularly limited, and examples thereof include noble metals such as Pt, Rh, Pd, Ce, Cu, V, Fe, Au, and Ag. No. Of these, Pt is preferably used.
- Pt is preferably used.
- the above-mentioned noble metals and the like may be used alone or in combination of two or more. With these catalysts, HC and CO contained in the exhaust gas can be reduced.
- the material of the catalyst support material layer used for supporting the catalyst is not particularly limited, and examples thereof include alumina and titer. Among them, alumina is preferably used.
- the honeycomb structure of the present invention supports a catalyst such as an alkali metal or an alkaline earth metal in addition to the above-mentioned catalyst within a range not to impair the object of the present invention. Is also good. This is a power that can purify NOx contained in exhaust gas using the honeycomb structure of the present invention.
- the shape is a columnar force.
- the honeycomb structure is not limited to a columnar shape if it is columnar.
- an arbitrary shape such as an elliptical column or a prism may be used.
- the ceramic particles constituting the honeycomb structure are not particularly limited, and examples thereof include nitride ceramics such as aluminum nitride, silicon nitride, boron nitride, and titanium nitride; Examples thereof include carbide ceramics such as silicon carbide, zirconium carbide, titanium carbide, tantalum carbide, and tungsten carbide. Among them, silicon carbide having high heat resistance, excellent mechanical properties, and high thermal conductivity is desirable.
- the porosity of the honeycomb structure is not particularly limited, but is preferably about 20 to 80%. If the porosity is less than 20%, the honeycomb structure of the present invention may be clogged immediately, while if the porosity exceeds 80%, the strength of the honeycomb structure is reduced and the honeycomb structure is easily broken. May be done.
- the porosity is determined by, for example, mercury intrusion method, Archimedes method and scanning electron microscope. It can be measured by a conventionally known method such as measurement by (SEM).
- the average pore diameter of the honeycomb structure is 5 to 100 ⁇ m. If the average pore size is less than 5 m, the particulates may easily become clogged. On the other hand, if the average pore diameter exceeds 100 m, the particulates may pass through the pores, failing to trap the particulates and failing to function as a filter.
- the average particle diameter of the ceramic particles constituting the honeycomb structure is preferably 1 to 100 m. Silicon is formed between the ceramic particles to join these ceramic particles.
- the weight ratio of ceramic particles to silicon is preferably 100 parts by weight of silicon to 100 parts by weight of ceramic particles.
- the sealing material sealed in the through-hole of the honeycomb structure is desirably a porous ceramic material.
- the sealing material is the same as the honeycomb structure.
- the adhesive strength between the two can be increased, and the porosity of the sealing material can be adjusted in the same manner as in the above-described honeycomb structure, so that the thermal expansion coefficient of the honeycomb structure can be improved.
- the thermal expansion coefficient of the sealing material can be matched, and there is a gap between the sealing material and the wall due to thermal stress during manufacturing or use, or the sealing material is in contact with the sealing material. It is possible to prevent the occurrence of cracks in the wall of the portion where the crack occurs.
- the sealing material is made of a porous ceramic
- the material is not particularly limited, and examples thereof include the same materials as the ceramic material constituting the honeycomb structure described above.
- the sealing material layers 13 and 14 are formed between the porous ceramic members 20 and on the outer periphery of the ceramic block 15. ing.
- the sealing material layer 14 formed between the porous ceramic members 20 also functions as an adhesive for binding the plurality of porous ceramic members 20, while the sealing material layer formed on the outer periphery of the ceramic block 15
- Layer 13 comprises the honeycomb structure 10 of the present invention in an internal combustion engine. When installed in the exhaust passage, it has a function of preventing the exhaust gas from leaking from the outer periphery of the ceramic block 15.
- the material constituting the sealing material layer is not particularly limited, and examples thereof include a material composed of an inorganic binder, an organic binder, inorganic fibers and Z or inorganic particles.
- the sealing material layers are formed by the forces formed between the porous ceramic members and on the outer periphery of the ceramic block. Or different materials. Furthermore, when the sealing material layers are made of the same material, the compounding ratio of the materials may be the same or different.
- Examples of the inorganic binder include silica sol and alumina sol. These may be used alone or in combination of two or more. Among the above inorganic binders, silica zonore is desirable.
- organic binder examples include polybutyl alcohol, methyl cellulose, ethyl cellulose, carboxymethyl cellulose and the like. These may be used alone or in combination of two or more. Among the above organic binders, carboxymethylcellulose is desirable.
- examples of the inorganic fibers include ceramic fibers such as silica-ano-remina, mullite, alumina, and silica. These may be used alone or in combination of two or more. Among the inorganic fibers, silica-alumina fibers are desirable.
- Examples of the inorganic particles include carbides and nitrides, and specific examples thereof include inorganic powders such as silicon carbide, silicon nitride, and boron nitride, and whiskers. 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 14 may be a porous material so that the exhaust gas may flow into the sealing material layer 14 even if the sealing material layer 14 has a dense physical strength.
- a catalyst is provided through a catalyst support material layer.
- a ceramic block to be supported is manufactured.
- the structure of the honeycomb structure of the present invention is an integrated filter composed entirely of one sintered body as shown in FIG. 3, first, the ceramic force as described above is used. Extrusion molding was carried out using a raw material paste containing ceramic powder and silicon powder as main components to produce a ceramic molded body having substantially the same shape as the integral honeycomb structure 30 shown in FIG. I do.
- the raw material paste is not particularly limited as long as the porosity of the ceramic block after manufacture is 20 to 80%.
- a binder and a dispersion medium solution are added to the above-mentioned ceramic powder and silicon powder. Can be mentioned.
- the binder is not particularly limited, and examples thereof include methylcellulose, carboxymethylcellulose, hydroxyethylcellulose, polyethylene glycol, and phenol resin.
- the amount of the binder is preferably about 110 parts by weight based on 100 parts by weight of the ceramic powder.
- the dispersion medium is not particularly limited, and examples thereof include an organic solvent such as benzene; an alcohol such as methanol, and water.
- the dispersion medium liquid is mixed in an appropriate amount so that the viscosity of the raw material paste falls within a certain range.
- a molding aid may be added to the raw material paste as needed.
- the molding aid is not particularly limited, and examples thereof include ethylene glycol, dextrin, fatty acid stone, and polyalcohol.
- the raw material paste may be added with a pore-forming agent such as a balloon, which is a fine hollow sphere containing an oxidizing ceramic, as a component, a spherical acrylic particle, a graphite, or the like, if necessary. Good.
- a pore-forming agent such as a balloon, which is a fine hollow sphere containing an oxidizing ceramic, as a component, a spherical acrylic particle, a graphite, or the like, if necessary. Good.
- the balloon is not particularly limited, and examples thereof include an alumina balloon, a glass micro balloon, a shirasu balloon, a fly ash balloon (FA balloon), and a mullite balloon. Of these, fly ash balloons are desirable.
- 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, or the like, and then sealed in a predetermined through-hole. A sealing material paste serving as a stopper is filled, and a sealing process for plugging the through hole is performed.
- 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%. Although it can be used, it is desirable 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 ceramic dried body sealed with the sealing material paste is degreased and fired at a firing temperature of 1400 to 1650 ° C under predetermined conditions, so that a porous ceramic force is also obtained. It is possible to manufacture a ceramic block in which the sintered body strength of the ceramic is also configured.
- the degreasing and firing conditions of the dried ceramic body may be the same as those conventionally used for manufacturing a porous structure having a porous ceramic strength.
- the honeycomb structure of the present invention is an aggregate-type filter configured by binding a plurality of porous ceramic members via a sealing material layer as shown in Fig. 1
- extrusion molding is performed using a raw material paste containing the above-described ceramic powder and silicon powder as main components to produce a formed body having a shape like the porous ceramic member 20 shown in FIG.
- the raw material paste may be the same as the raw material paste described in the integrated filter described above.
- a filler paste serving as a sealing material is sealed in predetermined through holes of the dried body, A sealing process for plugging the through hole is performed.
- the filler paste may be the same as the sealing material paste described in the integrated filter described above. Can be the same method as in the case of the integrated filter described above.
- a plurality of through holes are juxtaposed in the longitudinal direction across the partition walls by performing degreasing and baking on the dried body having undergone the above sealing treatment under the same conditions as in the case of the above-mentioned integrated filter.
- a porous ceramic member can be manufactured.
- a sealing material paste to be the sealing material layer 14 is applied in a uniform thickness on the side surface of the porous ceramic member to form a sealing material paste layer 51, and on this sealing material paste layer 51, Then, the step of sequentially laminating the other porous ceramic members 20 is repeated to produce a prismatic porous ceramic member 20 having a predetermined size.
- the material constituting the sealing material paste is the same as that described in the honeycomb structure of the present invention, and the description thereof is omitted here.
- the laminate of the porous ceramic members 20 is heated to dry and solidify the sealing material paste layer 51 to form the sealing material layer 14, and thereafter, using a diamond cutter or the like, for example, using a diamond cutter or the like, the outer periphery of the sealing material layer 14 is removed.
- a ceramic block composed of a plurality of porous ceramic members bound together via a sealing material layer can be manufactured.
- a sealing material layer 13 is formed on the outer periphery of the manufactured ceramic block using the sealing material paste.
- Each of the ceramic blocks manufactured as described above has a columnar shape, and the structure is as shown in Figs. 1 and 3.
- a catalyst is supported on the wall of the ceramic block manufactured by the above method via a catalyst support material layer.
- the material of the catalyst support material layer is the same as that described in the honeycomb structure of the present invention described above, and the description thereof is omitted here. In the following description, the case where alumina is used as the material of the catalyst support material layer will be described.
- Examples of the above-mentioned alumina include ⁇ -alumina, and this ⁇ -alumina can be prepared by a sol-gel method or the like.
- the inorganic binder is not particularly limited, and examples thereof include hydrated alumina.
- the fine powder is combined with pure water, and stirred using a stirrer or the like to prepare a slurry.
- the slurry is adhered to the wall surface of the ceramic block by spraying the slurry on the ceramic block, dipping the ceramic block in the slurry, or the like, so-called wet coating. .
- the ceramic block to which the slurry has been wash-coated is dried and baked at a predetermined temperature to form a catalyst support material layer on the wall surface of the ceramic block.
- Examples of the raw material for the aluminum-containing metal compound include metal compounds such as metal inorganic compounds and metal organic compounds.
- Examples of the above metal inorganic compound include Al (NO), A1C1, A10C1, A1PO, Al (S)
- Examples of the above-mentioned metal organic compound include metal alkoxide, metal acetyl acetonate, metal carboxylate and the like.
- Examples of the solvent include water, alcohol, diol, polyhydric alcohol, ethylene glycol, ethylene oxide, triethanolamine, xylene and the like. These solvents are used in a mixture of at least one kind in consideration of dissolution of the metal compound.
- a catalyst such as hydrochloric acid, sulfuric acid, nitric acid, acetic acid, and hydrofluoric acid may be added.
- a simple substance or a compound of Li, K, Ca, Sr, Ba, La, Pr, Nd, Si, and Zr may be added together with the metal compound.
- the solution of the aluminum-containing metal compound is impregnated into the wall of the ceramic block by a sol-gel method.
- a sol-gel method in order to spread the solution into all the pores, which are the gaps between the ceramic particles on the wall of the ceramic block, for example, a method of putting the ceramic block in a container, filling the solution with the solution, and degassing the solution. It is desirable to adopt a method in which the above solution is poured into the ceramic block and degassed from the other side.
- Examples of the degassing device include an aspirator and a vacuum pump.
- the solution was evaporated and gelled to fix the ceramic block on the surface of the ceramic particles, and excess solution was removed.
- Preliminary firing by heating to about 300-500 ° C.
- the alumina thin film formed on the surface of the ceramic particles becomes small fibers (needle-like particles) and stands, forming a so-called flocked structure and a thin film having a rough surface.
- the catalyst support material layer is formed on the wall of the ceramic block by firing at 500 to 1000 ° C for about 5 to 20 hours.
- the honeycomb structure of the present invention can be manufactured by supporting a catalyst on the catalyst support material layer formed by any of the above methods.
- the lower limit of the amount of the catalyst supported on the catalyst support material layer is a force calculated by substituting the opening ratio ⁇ of the ceramic block into the above equation (1). It is desirable that the value be equal to or smaller than the value obtained by substituting the aperture ratio ⁇ of the ceramic block into the equation (2).
- the method for supporting the above catalyst is not particularly limited, and examples thereof include an impregnation method, an evaporation to dryness method, an equilibrium adsorption method, an incipient wetness method, and a spray method.
- FIG. 5 is a cross-sectional view schematically showing one example of an exhaust gas purification apparatus for a vehicle in which the honeycomb structure of the present invention is installed.
- the exhaust gas purifying apparatus 600 mainly includes a honeycomb structure 60 of the present invention, a casing 630 covering the outside of the honeycomb structure 60, and a honeycomb structure.
- the holding seal material 620 is disposed between the structure 60 and the casing 630.
- the casing 630 has an introduction end connected to an internal combustion engine such as an engine at an end of the casing 630 where exhaust gas is introduced.
- a pipe 640 is connected, and the other end of the casing 630 is connected to an externally connected discharge pipe 65. 0 is connected.
- arrows indicate the flow of exhaust gas.
- the honeycomb structure 60 may be the honeycomb structure 10 shown in FIG. 1 or the honeycomb structure 30 shown in FIG.
- the exhaust gas discharged from the internal combustion engine such as the engine is introduced into the casing 630 through the introduction pipe 640, and the honeycomb structure 60 After passing through the wall (partition) from the through hole and collecting and purifying the particulates at the wall (partition), the particulate is discharged to the outside through the discharge pipe 650.
- the particulates collected on the walls (partitions) of the honeycomb structure 60 are oxidized by the above-mentioned regeneration method (1) or (2) by the catalyst supported on the walls.
- the honeycomb structure 60 is removed and the honeycomb structure 60 is regenerated.
- the opening ratio ⁇ of the ceramic block constituting the honeycomb structure and the supported amount of catalyst / 3 are expressed by the above formula (1). Therefore, the catalyst necessary for oxidizing and removing the particulates accumulated on the wall is sufficiently supported, and when the honeycomb structure is regenerated, The regeneration rate will be very good.
- the formed product was dried using a microwave drier to obtain a ceramic dried product, and a paste having the same composition as that of the formed product was filled in predetermined through-holes.
- a paste having the same composition as that of the formed product was filled in predetermined through-holes.
- Degreased at 400 ° C, and 1450 ° C, 1 hour under normal pressure argon atmosphere By sintering, the porosity is 50%, the average pore diameter is 20 / ⁇ , the size is 34.3mm X 34.3mm X 150.5mm, the cell density is 198 cells Z square inch, partition wall A porous ceramic member having a composite force of silicon carbide particles and silicon having a thickness of 0.43 mm was manufactured.
- a ceramic fiber made of alumina silicate as an inorganic fiber shot content: 3%, fiber length: 0.1 to 100 mm
- carbonized inorganic particles having an average particle diameter of 0.3 m Silicon powder 30.2% by weight
- silica sol as inorganic binder SiO content in sol
- 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 above-mentioned sealing material paste. Then, the sealing material paste layer was dried at 120 ° C. to form a sealing material layer on the outer periphery.
- the opening ratio of the obtained ceramic block was 55.9%.
- the supported amount of the catalyst calculated by substituting the aperture ratio into the above equation (1) is 2.8 gZL or more, and the supported amount of the catalyst calculated by substituting the above equation (2) is: 6. It is less than OgZL.
- ⁇ -alumina is formed on the wall (partition) of the ceramic block as a catalyst support material layer by the method described as the case of the supporting method (2) in the above embodiment, and Platinum was supported on the support material layer by the incipient wetness method.
- the supported amount of platinum was 3.OgZL (Example 1), 4.4gZL (Example 2), 6.OgZL (Example 3), 6.3gZL (Example 4), 2.6gZL (Comparative Example 1).
- Examples 5-8, Comparative Example 2 A porous ceramic member was manufactured in the same manner as (1) of Example 1 except that the cell density of the porous ceramic member was 316 cells Z square inches and the thickness of the partition walls was 0.36 mm.
- the supported amount of the catalyst calculated by substituting the opening ratio into the above equation (1) is equal to or greater than 3. OgZL, and the supported amount of the catalyst calculated by substituting the above equation (2) is: 6. It is less than 2gZL.
- a catalyst support material layer was formed in the same manner as (3) of Example 1, and platinum was carried on the catalyst support material layer to produce a cylindrical honeycomb structure.
- the supported amount of platinum was 3.4 OgZL (Example 5), 4.4 gZL (Example 6), 6.OgZL (Example 7), 6.3 gZL (Example 8), 2.6 gZL (Comparative Example). 2).
- a porous ceramic member was manufactured in the same manner as (1) of Example 1, except that the cell density of the porous ceramic member was 430 cells per square inch and the thickness of the partition walls was 0.31 mm.
- the supported amount of the catalyst calculated by substituting the opening ratio into the above equation (1) is 2.9 gZL or more, and the supported amount of the catalyst calculated by substituting the above equation (2) is: 6. It is less than lgZL.
- a catalyst support material layer was formed in the same manner as (3) of Example 1, and platinum was supported on the catalyst support material layer to produce a cylindrical honeycomb structure.
- the supported amount of platinum was 3.4 OgZL (Example 9), 4.4 gZL (Example 10), 6.OgZL (Example 11), 6.3 gZL (Example 12), 2.6 gZL (Comparative Example 3).
- a porous ceramic member was manufactured in the same manner as (1) of Example 1 except that the cell density of the porous ceramic member was 967 cells per square inch and the thickness of the partition walls was 0.20 mm.
- the supported amount of the catalyst calculated by substituting the aperture ratio into the above equation (1) is 2.8 gZL or more, and the supported amount of the catalyst calculated by substituting the above equation (2) is: 6. It is less than OgZL.
- (3) A catalyst support material layer was formed in the same manner as in (3) of Example 1, and platinum was supported on the catalyst support material layer to produce a columnar honeycomb structure. The supported amount of platinum was 3.4 OgZL (Example 13), 4.4 gZL (Example 14), 6.OgZL (Example 15), 6.3 g / L (Example 16), 2.6 gZL ( Comparative Example 4).
- a porous ceramic member was manufactured in the same manner as (1) of Example 1, except that the cell density of the porous ceramic member was 123 cells per square inch. That is, the thickness of the partition wall is 0.43 mm.
- the supported amount of the catalyst calculated by substituting the opening ratio into the above equation (1) is 1.8 gZL or more, and the supported amount of the catalyst calculated by substituting the above equation (2) is: 5. It is less than OgZL.
- a catalyst support material layer was formed in the same manner as (3) of Example 1, and platinum was supported on the catalyst support material layer to produce a columnar honeycomb structure.
- the supported amount of platinum was 2.0 OgZL (Example 17), 3.4 gZL (Example 18), 5.OgZL (Example 19), 5.3 g / L (Example 20), 1.7 gZL (Example 20). Comparative Example 5).
- a porous ceramic member was manufactured in the same manner as (1) of Example 5, except that the cell density of the porous ceramic member was 198 cells per square inch. That is, the thickness of the partition is 0.36 mm.
- the supported amount of the catalyst calculated by substituting the opening ratio into the above equation (1) is equal to or greater than 2.
- OgZL and the supported amount of the catalyst calculated by substituting the above equation (2) is: 5. It is less than 2gZL.
- Example 21 A catalyst support material layer was formed in the same manner as in (3) of Example 1, and platinum was carried on the catalyst support material layer to produce a columnar honeycomb structure.
- the supported amount of platinum was 2.0 OgZL (Example 21), 3.4 gZL (Example 22), 5.OgZL (Example 23), 5.3 g / L (Example 24), 1.7 gZL (Example 24). Comparative Example 6). [0141] Examples 25-28, Comparative Example 7
- a porous ceramic member was manufactured in the same manner as (1) of Example 9 except that the cell density of the porous ceramic member was set to 265 cells per square inch. That is, the thickness of the partition is 0.31 mm.
- the supported amount of the catalyst calculated by substituting the opening ratio into the above equation (1) is 1.9 gZL or more, and the supported amount of the catalyst calculated by substituting the above equation (2) is: 5. It is less than lgZL.
- a catalyst support material layer was formed in the same manner as in (3) of Example 1, and platinum was supported on the catalyst support material layer to produce a columnar honeycomb structure.
- the supported amount of platinum was 2.0 OgZL (Example 25), 3.4 gZL (Example 26), 5.OgZL (Example 27), 5.3 g / L (Example 28), 1.7 gZL (Example 28). Comparative Example 7).
- a porous ceramic member was manufactured in the same manner as (1) of Example 13 except that the cell density of the porous ceramic member was 634 cells and Z square inches. That is, the thickness of the partition is 0.20 mm 7.
- the supported amount of the catalyst calculated by substituting the opening ratio into the above equation (1) is 1.9 gZL or more, and the supported amount of the catalyst calculated by substituting the above equation (2) is: 5. It is less than lgZL.
- a catalyst support material layer was formed in the same manner as in (3) of Example 1, and platinum was supported on the catalyst support material layer to produce a columnar honeycomb structure.
- the supported amount of platinum was 2.4 OgZL (Example 29), 3.4 gZL (Example 30), 5.OgZL (Example 31), 5.3 g / L (Example 32), 1.7 gZL (Example 32). Comparative Example 8).
- a porous ceramic member was manufactured in the same manner as (1) of Example 1, except that the cell density of the porous ceramic member was 55 cells per square inch. That is, the thickness of the partition wall was 0.43 mm.
- a ceramic block having a sealing material layer formed on the outer periphery was produced. The opening ratio of the obtained ceramic block was 74.2%.
- the supported amount of catalyst calculated by substituting the opening ratio into the above equation (1) is 0.53 g / L or more, and the supported amount of catalyst calculated by substituting into the above equation (2) is 3.73gZL or less.
- a catalyst support material layer was formed in the same manner as in (3) of Example 1, and platinum was carried on the catalyst support material layer to produce a columnar honeycomb structure.
- the supported amount of platinum was 0.55 gZL (Example 33), 2.15 gZL (Example 34), 3.60 gZL (Example 35), 4.OOg / L (Example 36), 0.40 g / L L (Comparative Example 9).
- a porous ceramic member was manufactured in the same manner as (1) of Example 5, except that the cell density of the porous ceramic member was 79 cells per square inch. That is, the thickness of the partition wall was 0.36 mm.
- the supported amount of catalyst calculated by substituting the opening ratio into the above equation (1) is 0.48 g / L or more, and the supported amount of catalyst calculated by substituting into the above equation (2) is , 3. Use less than 68gZL.
- a catalyst support material layer was formed in the same manner as (3) of Example 1, and platinum was carried on the catalyst support material layer to produce a columnar honeycomb structure.
- the supported amount of platinum was 0.55 gZL (Example 37), 2.15 gZL (Example 38), 3.60 gZL (Example 39), 4.OOg / L (Example 40), 0.40 g / L L (Comparative Example 10).
- a porous ceramic member was manufactured in the same manner as (1) of Example 9 except that the cell density of the porous ceramic member was 107 cells per square inch. That is, the thickness of the partition is 0.31 mm.
- a catalyst support material layer was formed in the same manner as in (3) of Example 1, and platinum was supported on the catalyst support material layer to produce a columnar honeycomb structure.
- the supported amount of platinum was 0.55 gZL (Example 41), 2.15 gZL (Example 42), 3.60 gZL (Example 43), 4.OOg / L (Example 44), 0.40 g / L L (Comparative Example 11).
- a porous ceramic member was manufactured in the same manner as (1) of Example 13, except that the cell density of the porous ceramic member was 265 cells per square inch. That is, the thickness of the partition is 0.20 mm 7.
- the supported amount of the catalyst calculated by substituting the opening ratio into the above equation (1) is 0.46 g / L or more, and the supported amount of the catalyst calculated by substituting into the above equation (2) is , 3. Use less than 66gZL.
- a catalyst support material layer was formed in the same manner as (3) of Example 1, and platinum was supported on the catalyst support material layer to produce a columnar honeycomb structure.
- the supported amount of platinum was 0.55 gZL (Example 45), 2.15 gZL (Example 46), 3.60 gZL (Example 47), 4.OOg / L (Example 48), 0.40 g / L L (Comparative Example 12).
- the honeycomb structure according to Example 1-148 and Comparative Example 1-112 was installed in an exhaust gas purifying apparatus as shown in Fig. 5 provided in an exhaust passage of an engine. After operating at a rotation speed of 3,000 and a torque of 50 Nm for a predetermined time to collect particulates, the regeneration process of heating and regenerating the honeycomb structure to 550 ° C using an electric heater was repeated 20 times. The presence or absence of unburned particulates was observed. In addition, the presence or absence of unburned parts was examined by cutting the cam structure in a direction perpendicular to the longitudinal direction and using SEM to observe 15 points.
- Equation (1) Lower limit of catalyst loading calculated by substituting aperture ratio (g / f
- Equation (1) i: Lower limit of catalyst loading calculated by substituting aperture ratio (g / L)
- Example 4 Example 8, Example 12, Example 16, Example 20, Example 24, Example 28, Example 32, Example 36, Example 40, Example 44, and Example
- Example 48 In the honeycomb structure according to Example 48, although the relationship of the above formula (1) is satisfied with respect to the aperture ratio of the ceramic block, the relationship of the above formula (2) is not satisfied, and the relationship of the particulate After the collection and regeneration treatments were repeated 20 times, unburned particulates were observed, and the regeneration rate was slightly inferior.
- FIG. 1 is a perspective view schematically showing one example of an exhaust gas purifying filter of the present invention.
- FIG. 2 (a) is a perspective view schematically showing an example of a porous ceramic member constituting the exhaust gas purification honeycomb structure shown in FIG. 1, and FIG. FIG. 2 is a cross-sectional view of the porous ceramic member shown in FIG.
- FIG. 3 (a) is a perspective view schematically showing another example of the exhaust gas purifying honeycomb structure of the present invention, and (b) is a honeycomb structure shown in (a).
- FIG. 3 is a sectional view taken along line BB of FIG.
- FIG. 4 is a graph showing the relationship between the opening ratio a of a ceramic block and the amount of supported catalyst in a honeycomb structure for purifying exhaust gas of the present invention.
- FIG. 5 is a cross-sectional view schematically showing one example of an exhaust gas cleaning apparatus using the exhaust gas cleaning honeycomb structure of the present invention.
- FIG. 6 is a sectional perspective view schematically showing an example of a catalyst carrier used in a conventional exhaust gas purification system.
- FIG. 7 is a cross-sectional perspective view schematically showing an example of a conventional honeycomb structure for exhaust gas purification.
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- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Geometry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Ceramic Engineering (AREA)
- Organic Chemistry (AREA)
- Structural Engineering (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Processes For Solid Components From Exhaust (AREA)
- Filtering Materials (AREA)
- Catalysts (AREA)
- Filtering Of Dispersed Particles In Gases (AREA)
Abstract
Description
Claims
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EP04818205A EP1649917A4 (en) | 2003-11-07 | 2004-11-05 | BODY WITH HONEYCOMB STRUCTURE |
JP2005515321A JPWO2005044422A1 (ja) | 2003-11-07 | 2004-11-05 | ハニカム構造体 |
US11/368,401 US7541006B2 (en) | 2003-11-07 | 2006-03-07 | Honeycomb structured body |
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JP2003378708 | 2003-11-07 | ||
JP2003-378708 | 2003-11-07 |
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US11/368,401 Continuation US7541006B2 (en) | 2003-11-07 | 2006-03-07 | Honeycomb structured body |
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WO2005044422A1 true WO2005044422A1 (ja) | 2005-05-19 |
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US (1) | US7541006B2 (ja) |
EP (1) | EP1649917A4 (ja) |
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- 2004-11-05 WO PCT/JP2004/016442 patent/WO2005044422A1/ja active Application Filing
- 2004-11-05 JP JP2005515321A patent/JPWO2005044422A1/ja not_active Withdrawn
- 2004-11-05 EP EP04818205A patent/EP1649917A4/en not_active Withdrawn
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2006
- 2006-03-07 US US11/368,401 patent/US7541006B2/en active Active
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JP2001137714A (ja) | 1999-11-16 | 2001-05-22 | Ibiden Co Ltd | 触媒およびその製造方法 |
EP1277714A1 (en) | 2000-04-14 | 2003-01-22 | Ngk Insulators, Ltd. | Honeycomb structure and method for its manufacture |
JP2002253916A (ja) * | 2001-03-01 | 2002-09-10 | Ngk Insulators Ltd | ハニカムフィルター、及びその製造方法 |
WO2002096827A1 (fr) | 2001-05-31 | 2002-12-05 | Ibiden Co., Ltd. | Corps fritte ceramique poreux et procede permettant sa production, et filtre a gasoil particulaire |
EP1403231A1 (en) | 2001-05-31 | 2004-03-31 | Ibiden Co., Ltd. | Porous ceramic sintered body and method of producing the same, and diesel particulate filter |
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Non-Patent Citations (1)
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7611764B2 (en) | 2003-06-23 | 2009-11-03 | Ibiden Co., Ltd. | Honeycomb structure |
JPWO2007058006A1 (ja) * | 2005-11-18 | 2009-04-30 | イビデン株式会社 | ハニカム構造体 |
JP2009521303A (ja) * | 2005-12-24 | 2009-06-04 | ユミコア・アクチエンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト | セラミックハニカム体を触媒により被覆する方法 |
US8278236B2 (en) * | 2005-12-24 | 2012-10-02 | Umicore Ag & Co. Kg | Method for catalytically coating ceramic honeycomb bodies |
US9278347B2 (en) | 2005-12-24 | 2016-03-08 | Umicore Ag & Co. Kg | Catalytically coated ceramic honeycomb bodies |
Also Published As
Publication number | Publication date |
---|---|
US20060217262A1 (en) | 2006-09-28 |
US7541006B2 (en) | 2009-06-02 |
JPWO2005044422A1 (ja) | 2007-11-29 |
EP1649917A1 (en) | 2006-04-26 |
EP1649917A4 (en) | 2006-07-05 |
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