WO2007000847A1 - ハニカム構造体 - Google Patents
ハニカム構造体 Download PDFInfo
- Publication number
- WO2007000847A1 WO2007000847A1 PCT/JP2006/307955 JP2006307955W WO2007000847A1 WO 2007000847 A1 WO2007000847 A1 WO 2007000847A1 JP 2006307955 W JP2006307955 W JP 2006307955W WO 2007000847 A1 WO2007000847 A1 WO 2007000847A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cam
- unit
- sealing material
- material layer
- honeycomb
- Prior art date
Links
- 239000003566 sealing material Substances 0.000 claims abstract description 67
- 239000003054 catalyst Substances 0.000 claims description 52
- 239000010954 inorganic particle Substances 0.000 claims description 20
- 239000012784 inorganic fiber Substances 0.000 claims description 17
- 238000000746 purification Methods 0.000 abstract description 25
- 239000000463 material Substances 0.000 description 68
- 241000264877 Hippospongia communis Species 0.000 description 46
- 239000007789 gas Substances 0.000 description 42
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 35
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 27
- 239000011230 binding agent Substances 0.000 description 26
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 20
- 239000000377 silicon dioxide Substances 0.000 description 18
- 238000005259 measurement Methods 0.000 description 15
- 239000002245 particle Substances 0.000 description 13
- 239000000835 fiber Substances 0.000 description 11
- 229910052697 platinum Inorganic materials 0.000 description 10
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 10
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 8
- 229910002091 carbon monoxide Inorganic materials 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 6
- 229910010271 silicon carbide Inorganic materials 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- OJMOMXZKOWKUTA-UHFFFAOYSA-N aluminum;borate Chemical compound [Al+3].[O-]B([O-])[O-] OJMOMXZKOWKUTA-UHFFFAOYSA-N 0.000 description 5
- 238000013329 compounding Methods 0.000 description 5
- 238000010304 firing Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 229920000609 methyl cellulose Polymers 0.000 description 4
- 235000010981 methylcellulose Nutrition 0.000 description 4
- 239000001923 methylcellulose Substances 0.000 description 4
- 230000002093 peripheral effect Effects 0.000 description 4
- NWAHZABTSDUXMJ-UHFFFAOYSA-N platinum(2+);dinitrate Chemical compound [Pt+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O NWAHZABTSDUXMJ-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- -1 zircoure Chemical compound 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000001354 calcination Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 229910000510 noble metal Inorganic materials 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- 229910052580 B4C Inorganic materials 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 229940105329 carboxymethylcellulose Drugs 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 2
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 229910052878 cordierite Inorganic materials 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001739 density measurement Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 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
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000002612 dispersion medium Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229910052863 mullite Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- 230000035939 shock Effects 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
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229910052684 Cerium Inorganic materials 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
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 238000000691 measurement method 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
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000003960 organic solvent Substances 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
- 238000002459 porosimetry Methods 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000010938 white gold Substances 0.000 description 1
- 229910000832 white gold Inorganic materials 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 229910052727 yttrium 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
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/86—Catalytic processes
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/42—Platinum
-
- 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
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
-
- 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
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/24—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing alkyl, ammonium or metal silicates; containing silica sols
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/10—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
- C04B35/111—Fine ceramics
- C04B35/117—Composites
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/14—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silica
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/16—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
- C04B35/18—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay rich in aluminium oxide
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/46—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/6303—Inorganic additives
- C04B35/6316—Binders based on silicon compounds
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/71—Ceramic products containing macroscopic reinforcing agents
- C04B35/78—Ceramic products containing macroscopic reinforcing agents containing non-metallic materials
- C04B35/80—Fibres, filaments, whiskers, platelets, or the like
-
- 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
- C04B37/00—Joining burned ceramic articles with other burned ceramic articles or other articles by heating
- C04B37/003—Joining burned ceramic articles with other burned ceramic articles or other articles by heating by means of an interlayer consisting of a combination of materials selected from glass, or ceramic material with metals, metal oxides or metal salts
- C04B37/005—Joining burned ceramic articles with other burned ceramic articles or other articles by heating by means of an interlayer consisting of a combination of materials selected from glass, or ceramic material with metals, metal oxides or metal salts consisting of glass or ceramic material
-
- 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
- C04B38/0016—Honeycomb structures assembled from subunits
-
- 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
- F01N13/00—Exhaust or silencing apparatus characterised by constructional features ; Exhaust or silencing apparatus, or parts thereof, having pertinent characteristics not provided for in, or of interest apart from, groups F01N1/00 - F01N5/00, F01N9/00, F01N11/00
- F01N13/009—Exhaust or silencing apparatus characterised by constructional features ; Exhaust or silencing apparatus, or parts thereof, having pertinent characteristics not provided for in, or of interest apart from, groups F01N1/00 - F01N5/00, F01N9/00, F01N11/00 having two or more separate purifying devices arranged in series
- F01N13/0097—Exhaust or silencing apparatus characterised by constructional features ; Exhaust or silencing apparatus, or parts thereof, having pertinent characteristics not provided for in, or of interest apart from, groups F01N1/00 - F01N5/00, F01N9/00, F01N11/00 having two or more separate purifying devices arranged in series the purifying devices are arranged in a single housing
-
- 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
-
- 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
- C04B2111/00034—Physico-chemical characteristics of the mixtures
- C04B2111/00129—Extrudable mixtures
-
- 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
- C04B2111/00034—Physico-chemical characteristics of the mixtures
- C04B2111/00198—Characterisation or quantities of the compositions or their ingredients expressed as mathematical formulae or equations
-
- 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
-
- 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
- C04B2111/0081—Uses not provided for elsewhere in C04B2111/00 as catalysts or catalyst carriers
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3217—Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
- C04B2235/322—Transition aluminas, e.g. delta or gamma aluminas
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3418—Silicon oxide, silicic acids or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5208—Fibers
- C04B2235/5216—Inorganic
- C04B2235/522—Oxidic
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5208—Fibers
- C04B2235/5216—Inorganic
- C04B2235/522—Oxidic
- C04B2235/5224—Alumina or aluminates
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5208—Fibers
- C04B2235/526—Fibers characterised by the length of the fibers
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5208—Fibers
- C04B2235/5264—Fibers characterised by the diameter of the fibers
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5276—Whiskers, spindles, needles or pins
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/54—Particle size related information
- C04B2235/5418—Particle size related information expressed by the size of the particles or aggregates thereof
- C04B2235/5436—Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/54—Particle size related information
- C04B2235/5418—Particle size related information expressed by the size of the particles or aggregates thereof
- C04B2235/5445—Particle size related information expressed by the size of the particles or aggregates thereof submicron sized, i.e. from 0,1 to 1 micron
-
- 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
- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/02—Aspects relating to interlayers, e.g. used to join ceramic articles with other articles by heating
- C04B2237/04—Ceramic interlayers
- C04B2237/06—Oxidic interlayers
- C04B2237/064—Oxidic interlayers based on alumina or aluminates
-
- 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
- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/02—Aspects relating to interlayers, e.g. used to join ceramic articles with other articles by heating
- C04B2237/04—Ceramic interlayers
- C04B2237/08—Non-oxidic interlayers
- C04B2237/083—Carbide interlayers, e.g. silicon carbide interlayers
-
- 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
- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates
- C04B2237/32—Ceramic
- C04B2237/34—Oxidic
- C04B2237/341—Silica or silicates
-
- 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
- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates
- C04B2237/32—Ceramic
- C04B2237/34—Oxidic
- C04B2237/343—Alumina or aluminates
-
- 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
- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates
- C04B2237/32—Ceramic
- C04B2237/34—Oxidic
- C04B2237/345—Refractory metal oxides
- C04B2237/346—Titania or titanates
-
- 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
- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/50—Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating
- C04B2237/70—Forming laminates or joined articles comprising layers of a specific, unusual thickness
- C04B2237/704—Forming laminates or joined articles comprising layers of a specific, unusual thickness of one or more of the ceramic layers or articles
-
- 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
- F01N2330/00—Structure of catalyst support or particle filter
- F01N2330/06—Ceramic, e.g. monoliths
-
- 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
- F01N2330/00—Structure of catalyst support or particle filter
- F01N2330/10—Fibrous material, e.g. mineral or metallic wool
-
- 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
- F01N2330/00—Structure of catalyst support or particle filter
- F01N2330/30—Honeycomb supports characterised by their structural details
-
- 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
- F01N2450/00—Methods or apparatus for fitting, inserting or repairing different elements
- F01N2450/28—Methods or apparatus for fitting, inserting or repairing different elements by using adhesive material, e.g. cement
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/10—Internal combustion engine [ICE] based vehicles
- Y02T10/12—Improving ICE efficiencies
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24149—Honeycomb-like
Definitions
- the present invention relates to a her cam structure.
- a catalyst carrier used for exhaust gas purification in which a catalyst support layer such as activated alumina is provided inside a through-hole of a her cam structure is known.
- the cell shape of the honeycomb structure is hexagonal or circular, the cell density is 600 to 1200 cells Zinch 2 (cpsi), and the depth is within 100 m from the surface It is known that the portion existing in the catalyst is 80% or more of the volume of the catalyst support layer (see, for example, JP-A-10-263416).
- the present invention has been made in view of such a problem, and it is possible to increase the purification rate of exhaust gas by setting the apparent density and specific surface area of the her cam structure in a suitable range.
- An object of the present invention is to provide a double cam structure.
- the present invention employs the following means in order to achieve the above-described object. That is, the honeycomb structure of the present invention is
- a nose-cam structure comprising a her cam unit having a plurality of through holes, and a sealing material layer that joins two or more her cam units on the outer surface with the through holes being open.
- a (gZcm 3 ) is the product of the apparent density of the honeycomb unit and the volume fraction of the honeycomb unit occupying the entire honeycomb structure, and the apparent density of the sealing material layer and the When the product of the volume ratio of the sealing material layer occupying the whole is B (g / cm 3 ), and the specific surface area per unit volume of the Hercam structure is C (m 2 / L), 2 ⁇ A / B ⁇ 0. 0002 XC + 5 (28000 ⁇ C).
- This her cam structure has an apparent density that the her cam unit occupies in the entire her cam structure, an apparent density that the seal material layer occupies in the entire her cam structure, -It defines the specific surface area per unit volume of the cam structure.
- an apparent density that the seal material layer occupies in the entire her cam structure -It defines the specific surface area per unit volume of the cam structure.
- the apparent density of the hard cam unit and the apparent density of the sealing material layer formed on the outer surface of the two-cam unit may affect the ease of heating and cooling of the honeycomb structure. It is done.
- the inventors of the present invention have an apparent density of a her cam unit and a seal material layer, and a her cam structure, to a her cam structure in which two or more her cam units having a plurality of through holes are joined.
- the product of the apparent density of the her cam unit and the volume fraction of the her cam unit in the entire her cam structure is A (gZcm 3 )
- B (g / cm 3 ) is the product of the apparent density of the sealing material layer and the volume ratio of the sealing material layer to the entire Hercam structure
- C is the specific surface area per unit volume of the Hercam structure.
- the specific surface area C is most preferable to satisfy at least more preferably tool 38000m 2 / L to satisfy the above 35000m 2 / L.
- the C value is 35 OOOm 2 ZL or more
- the catalyst can be further highly dispersed.
- the specific surface area C satisfies 70000 m 2 / L or less.
- the product A satisfies 0.2 gZcm 3 or more and 0.5 g / cm 3 or less.
- the product A is less than 0. 2gZcm 3, ha - strong cam unit
- it exceeds 0.5 gZcm 3 the heat capacity of the Hercam structure increases and it may take time to reach the activation temperature of the catalyst.
- the thickness of the sealing material layer is 0.1 to 2. Omm. If this thickness is less than 0.1 mm, sufficient bonding strength between the hard cam units may not be obtained. If it exceeds 2. Omm, the volume of the sealing material layer, which is a part that is not so much related to the catalytic reaction, may be increased. Since it becomes relatively large, it is not preferable from the viewpoint of the purification rate of exhaust gas.
- the her cam unit includes inorganic particles and inorganic fibers.
- the inorganic particles include one or two or more types of particles whose forces are also selected, such as alumina, silica, titania, zircoure, ceria, mullite and zeolite.
- the inorganic fibers include one or two or more types of fiber wishes selected from alumina, silica, silicon carbide, silica alumina, glass, potassium titanate, and aluminum borate. In this way, a high cam unit having a high specific surface area and high strength can be produced relatively easily.
- the inorganic noda include one or more binders selected by force such as alumina sol, silica sol, titasol and water glass. In this way, sufficient strength can be obtained even at a low firing temperature.
- the sealing material layer preferably comprises inorganic particles and inorganic fibers.
- the inorganic particles include those described above, and one or more types of particles that are selected from force such as silicon carbide, boron carbide, and silicon nitride.
- examples of the inorganic fiber include one or two or more types of fibers that have a force selected such as those described above.
- examples of the inorganic binder include one or two or more binders that are selected from the above-described forces. In this way, the thermal shock resistance of the her cam structure can be improved, and a sealing material layer having a desired apparent density can be formed relatively easily.
- the catalyst is supported in the hard cam structure of the present invention.
- the catalyst one that purifies CO, HC, NOx, etc. contained in the exhaust gas, such as noble metal It may be an alkali metal, an alkaline earth metal, or an oxide compound.
- the noble metal for example, one or more kinds such as platinum, noradium and rhodium are also selected, and as the alkali metal, for example, one or more kinds such as sodium and potassium are selected.
- the alkaline earth metal for example, magnesium One or more selected from the power such as and barium.
- examples of the acid compound include those having a mouth-buckite structure (LaCoO, LaMnO, etc.) and CeO, etc.
- oxide compound having a perovskite structure examples include one or more elements in which the A site of the bottom buxite structure (general formula ABO) is selected from forces such as La, Y, and Ce.
- the B site of the general formula preferred by La is one or more elements selected from Fe, Co, Ni and Mn.
- the Hercam structure of the present invention carrying a catalyst may be used for exhaust gas purification of vehicles.
- FIG. 1 is an explanatory diagram of a honeycomb structure 20 of the present embodiment.
- FIG. 2 is an explanatory diagram of the honeycomb unit 10 of the present embodiment, (a) is a perspective view, and (b) is an XX cross-sectional view of (a).
- FIG. 3 A preferred range of AZB and specific surface area C per unit volume of the hard cam structure 20.
- FIG. 4 An explanatory view of the exhaust gas purification measuring device 60.
- FIG. 5 is an explanatory diagram showing the relationship between AZB and specific surface area C per unit volume.
- FIG. 1 is an explanatory view of the honeycomb structure 20 of the present embodiment
- FIG. 2 is an explanatory view of the honeycomb unit 10
- (a) is a perspective view
- (b) is an X— It is X sectional drawing.
- This hard cam structure 20 is a hard cam for a catalytic converter that has a function of purifying harmful substances (for example, hydrocarbon HC, carbon dioxide CO, nitrogen oxide NOx, etc.) in engine exhaust gas. It is configured as a structure.
- This her-cam structure 20 is a prism having a plurality of through holes 12 arranged in parallel along the longitudinal direction.
- the two or more her cam units 10 formed in a shape, the her cam unit 10 having a through-hole 12 open, a seal material layer 26 joined at the outer surface 13, and a seal material layer 26 joined.
- the coating material layer 27 that covers the outer peripheral surface of the two or more her cam units 10 where the through-holes 12 are not opened is provided.
- This her-cam structure 20 has a product of the apparent density of the her-cam unit 10 and the volume ratio of the her-cam unit 10 in the entire her-cam structure 20 as A (g / cm 3 ).
- B (g / cm 3 ) is the product of the apparent density of layer 26 and the volume fraction of sealing material layer 26 occupying the entire hard cam structure 20, and the specific surface area per unit volume of the hard cam structure 20
- C m 2 / L
- A is obtained by multiplying the apparent density (dry weight Z volume) of the hard cam unit 10 by the ratio of the volume of the hard cam unit 10 to the total volume of the hard cam structure 20.
- the volume used to calculate this apparent density is the volume including pores and through-holes (cells). This A preferably satisfies 0.2 g / cm 3 ⁇ A ⁇ 0.5 g / cm 3 . If A is less than 0.2 g Zcm 3 , the strength of the her cam unit may be weak, and if it exceeds 0.5 g Zcm 3 , the heat capacity of the her cam structure will increase and it will take time to reach the activation temperature of the catalyst. Sometimes it takes. B represents the apparent density (dry weight Z volume) of the sealing material layer 26 multiplied by the ratio of the volume of the sealing material layer 26 to the total volume of the two-cam structure 20.
- the specific surface area C per unit volume is calculated by calculating the specific surface area per unit volume including pores and cells of the Hercam unit by measuring the BET specific surface area of the HerCam unit 10 and measuring the BET specific surface area. This is the product of the ratio of the volume of the Her-cam unit 10 to the total volume of the Her-cam structure 20.
- the specific surface area C is required to be 28000m 2 / L or more, and most preferably more preferably tool 38000m 2 ZL is 35000m 2 ZL more.
- the specific surface area C per unit volume preferably satisfies 70000 m 2 ZL or less.
- FIG. 3 shows a preferred range of AZB, which is the ratio of A and B, and specific surface area C per unit volume of the Hercom structure 20. If the Hercam structure 20 is manufactured so as to be included in this range, the exhaust gas purification performance Can be increased.
- the her cam unit 10 has a square cross section perpendicular to the through-hole 12, and the outer cam cam body 20 formed by joining a plurality of her cam units 10 has a circular outer shape. It is formed in a column shape.
- the shape of the her cam unit 10 may be, for example, a rectangular, hexagonal or fan-shaped cross section of the surface perpendicular to the through hole 12, and the shape of the honeycomb structure 20 may be, for example, a through hole
- the cross section of the surface orthogonal to the hole 12 may be prismatic or elliptical.
- the through hole 12 formed in the honeycomb unit 10 has a square cross section.
- the cross section may be triangular or hexagonal.
- Thickness of wall 15 between through-holes 12 (wall thickness) [Between 0.05 and 0.35 mm of force S, preferably 0.10 to 0.30 mm, more preferably S, 0.15 to 0 25mm is most preferred. If the wall thickness is less than 0.05 mm, the strength of the her cam unit 10 decreases, and if it exceeds 0.35 mm, it may be difficult for the exhaust gas to contact the catalyst supported inside the wall 15. Catalyst performance may be reduced.
- the number of through-holes per unit cross-sectional area is preferably 15.5 to 186 Zcm 2 (100 to 1200 cpsi), and 46.5 to 170.5 Zcm 2 (300 to: L lOOcpsi) ) Force is preferred, 62.0 to 155 Zcm 2 (400 to 1000 cpsi) is most preferred. If the number of through-holes is less than 15.5 Zcm 2 , the area of the wall in contact with the exhaust gas inside the honeycomb unit will be small, and if it exceeds 186 holes / cm 2 , the pressure loss will increase, and This is because the manufacture of unit 10 becomes difficult.
- the porosity of the hammer unit 10 is preferably 30 to 80%, and preferably 40 to 70%. When the porosity is less than 30%, the apparent density may increase, and when the porosity exceeds 80%, the strength may decrease.
- the cam unit as the size of 10, more preferably tool 8 ⁇ 30Cm 2 that the cross-sectional area of the unit is formed by the preferred tool 6 ⁇ 40Cm 2 form with 5 to 50 cm 2 Most preferably.
- the specific surface area per unit volume of the hard cam structure 20 can be kept large, the catalyst can be highly dispersed, and even if an external force such as thermal shock or vibration is applied, the hard cam The shape as a structure can be maintained.
- the ratio of the total cross-sectional area of the hard cam unit 10 to the cross-sectional area of the hard structure 20 (hereinafter referred to as unit area ratio) is preferably 85% or more, and preferably 90% or more. Is better Good. If this ratio is less than 85%, the surface area on which the catalyst is supported becomes relatively small, or the pressure loss becomes large, which is not preferable.
- the Hercom unit 10 is manufactured by including alumina particles as inorganic particles, aluminum borate whisker as inorganic fibers, and silica sol as an inorganic noda.
- the inorganic particles for example, one kind or two or more kinds of particles selected by force such as silica, titania, zircoure, ceria, mullite and zeolite may be contained.
- the inorganic fiber may include one or two or more types of fiber wishes selected from alumina, silica, silicon carbide, silica alumina, glass, potassium titanate, and the like.
- the inorganic binder for example, one kind or two or more kinds of binders selected by force such as alumina sol, titasol and water glass may be included.
- the sealing material layer 26 contains silicon carbide as inorganic particles, alumina fibers as inorganic fibers, and silica sol as an inorganic binder.
- the inorganic particles may include one or two or more types of particles whose power is selected, such as those described in the above-described Hercom unit 10, boron carbide, silicon nitride and the like.
- the intermediate force described in the above-mentioned honeycomb unit 10 may be selected.
- the porosity of the sealing material layer 26 is preferably 10 to 80%, more preferably 15 to 70%. If the porosity is less than 10%, the apparent density increases and the catalyst activation temperature may be reached, and if the porosity exceeds 80%, the strength for joining the hard cam unit 10 is unfavorable.
- the supported amount of the catalyst is preferably 1 to 5 gZL in terms of the weight of the catalyst per unit volume of the Hercom structure 20.
- the method for supporting the catalyst is not particularly limited, but the impregnation method is preferable because it is relatively simple.
- raw material paste is prepared by mixing alumina particles as inorganic particles, aluminum borate whisker as inorganic fibers, and silica sol as an inorganic binder. Examples of inorganic particles, inorganic fibers, and inorganic noinders are described in the above-mentioned Hercom unit 10. You may use what was clarified. In addition to these, an organic binder, a dispersion medium and a molding aid may be appropriately added to the raw material paste in accordance with the moldability.
- the organic binder examples include one or more organic binders selected from methenoresenorelose, canoleboxymethylenoresenorelose, hydroxyethinoresenorelose, polyethylene glycol, phenol resin, and epoxy resin. It is done.
- the blending amount of the organic binder is preferably 1 to: LO parts by mass with respect to 100 parts by mass in total of the alumina particles, aluminum borate whisker and silica sol.
- the dispersion medium include water, organic solvents (such as benzene), and alcohols (such as methanol).
- the molding aid include ethylene glycol, dextrin, fatty acid, fatty acid stannic acid and polyalcohol. Mixing of the raw materials may be sufficiently kneaded with an mixer or the like using a mixer or a writer.
- the method for forming the raw material paste is, for example, formed into a honeycomb shape having through holes by extrusion molding or the like.
- the obtained molded body is dried.
- a microwave dryer or a hot air dryer is used as the dryer.
- the degreasing conditions are appropriately selected depending on the type and amount of the organic substance contained in the molded body, but are preferably about 400 ° C. and 2 hours.
- the dried and degreased compact is fired at 600 to 1000 ° C. When the firing temperature is less than 600 ° C, the sintering of inorganic particles does not proceed and the strength of the no-cam structure becomes low. When the firing temperature exceeds 1000 ° C, the sintering of inorganic particles proceeds too much and the specific surface area is increased. This is because the size of the catalyst may be small and the supported catalyst may not be sufficiently dispersed. Through these steps, a her cam unit 10 having a plurality of through holes is obtained.
- a sealing material paste as a sealing material layer is applied to the resulting her cam unit 10, the honeycomb units 10 are sequentially joined, and then dried and solidified to form the sealing material layer 26.
- a no-cam unit assembly is produced.
- the sealing material paste is prepared by mixing silicon carbide particles as inorganic particles, alumina fibers as inorganic fibers, and silica sol as an inorganic binder.
- the sealing material paste for example, a mixture of an inorganic binder and inorganic particles, a mixture of an inorganic binder and inorganic fibers, a mixture of an inorganic binder, inorganic particles and inorganic fibers, or the like is used. Can do.
- Inorganic particles, inorganic fibers and As the inorganic binder for example, those described for the sealing material layer 26 described above may be used. Further, an organic binder may be added to the sealing material paste. Examples of the organic binder include one or more organic binders whose strengths are selected such as polybutyl alcohol, methyl cellulose, ethyl cellulose, and carboxymethyl cellulose.
- This sealing material paste is appropriately prepared so as to satisfy the range of the above formula (1) after the sealing material paste is solidified.
- the thickness of the sealing material layer to which the her cam unit 10 is joined is preferably 0.1 to 2 Omm. If the thickness of the sealing material layer is less than 0.1 mm, sufficient bonding strength cannot be obtained. On the other hand, if it exceeds 2.
- the specific surface area per unit volume of the her cam structure is lowered, which is not preferable. This is also the force that the sealing material layer does not function as a catalyst carrier.
- the number of the hard cam units 10 to be joined may be appropriately determined according to the size of the hard cam structure 20 to be used.
- the two-cam unit assembly is appropriately cut and polished so as to be the size of the two-cam structure 20, and the through hole is opened, and the outer peripheral surface (side surface) is coated.
- the paste is applied and dried and solidified to form the coating material layer 27. By doing so, the outer peripheral surface can be protected and the strength can be increased.
- the coating material paste may have the same composition and blending ratio as the sealing material, or may have a different composition and blending ratio.
- the thickness of the coating material layer is preferably 0.1-2 mm.
- the catalyst is supported on the obtained no-cam carrier.
- white gold is supported as an oxidation catalyst.
- a catalyst-containing solution is prepared, and after the honeycomb carrier is immersed in this solution, it is pulled up and excess solution remaining in the through holes 12 is removed by suction. Then, drying is performed at 80 to 200 ° C., and calcination is performed at 500 to 700 ° C., whereby the two-cam structure 20 on which the catalyst is supported can be obtained.
- the step of immersing the honeycomb carrier in the catalyst solution and calcining may be repeated for each catalyst.
- the amount of catalyst supported is appropriately selected depending on the type and combination thereof.
- the catalyst may be supported after the her cam carrier is manufactured, may be performed at the stage of raw inorganic particles, or may be performed at the stage of manufacturing the her cam unit 10.
- 2 ⁇ AZB ⁇ 0.0002 XC + 5 (28000 ⁇ C) is satisfied, so that the purification rate of exhaust gas is increased. Can do.
- the thickness of the sealing material layer is set to 0.1 to 2 Omm, it is possible to obtain a sufficient bonding strength between the her cam units, and to reduce the portion of the exhaust gas by reducing the portion not much related to the catalytic reaction.
- the purification rate can be increased.
- ⁇ alumina particles (KC-501 made by Sumitomo Chemical Co., Ltd., average particle size 1 ⁇ m) 2250 parts by mass, aluminum borate whisker (average fiber length 20 ⁇ m, average fiber diameter 0.5 m) 680 parts by mass , silica sol (solid concentration 30 wt 0/0) 2600 parts by weight of the inorganic Noinda, methylcellulose (MC) 320 parts by weight of an organic binder, water, a plasticizer (glycerin) and a lubricant (trade name Yunirupu; NOF (strain )) was added in an appropriate amount and mixed and kneaded to obtain a mixed composition.
- silica sol solid concentration 30 wt 0/0
- this mixed composition was extruded into a prism shape in which a plurality of through-holes juxtaposed along the longitudinal direction was formed by an extruder, thereby obtaining a raw molded body.
- the green molded body was sufficiently dried using a microwave dryer and a hot air dryer, and degreased by holding at 400 ° C. for 2 hours. Then, hold for 2h at 800 ° C and fire, prismatic shape (34.3mm x 34.3mm x 75mm), cell density 93 pieces Zcm 2 (600cpsi), wall thickness 0.2mm, cell shape square
- the shape of a hard cam unit 10 hereinafter, this sample is referred to as “no-cam 1” was obtained.
- Table 1 summarizes the numerical values of the constituent material (base material), silica sol, methyl cellulose, and the like, and the firing temperature. Table 1 also shows numerical values such as the apparent density, porosity, and specific surface area per unit volume as sample measurement results, and also summarizes the contents of Harm 2 to 5, which will be described later.
- the apparent density of No-Cam 1 obtained was 0.45 g / cm 3
- the porosity was 60%
- the specific surface area per unit volume was 40000 m 2 ZL. The method for calculating the apparent density, porosity, and specific surface area per unit volume will be described later.
- ⁇ two-cam] to 5 all have a wall thickness of 0.2IM, a cell density of 600cps i, and an aperture ratio of 65.1%.
- silicon carbide particles (average particle size 0.5 m) 3600 parts by mass, alumina fibers (average fiber diameter 10 / ⁇ ⁇ , average fiber length 100 m, aspect ratio 10) 5500 parts by mass, inorganic binder preparation of silica sol (solid concentration 30 wt 0/0) 3000 parts by weight, the carboxy methyl cellulose (CMC) 50 parts by weight, and water as an organic binder mixed with an appropriate amount of sealing material paste (this is a sheet Lumpur material 1) of Te did.
- Table 2 summarizes the numerical values of the constituent material of this sealing material 1, the amount of silica sol, the amount of CMC, etc.
- Table 2 also shows the measurement results of the apparent density and porosity after solidification as the evaluation results of the sealing material, and also shows the contents related to the honeycombs 2 to 5 described later.
- the sealing material paste was applied to the outer surface 13 of the her cam 1 so that the thickness was 1 mm, and the four her cam units 10 and 4 horizontal members were joined to obtain a joined body. Then, the joined body is cut into a cylindrical shape using a diamond cutter so that the front surface of the joined body is substantially point-symmetric, and the above-mentioned sealing material paste is 0.5 mm thick on a circular outer surface having no through hole.
- the coating material layer 27 was formed on the outer peripheral surface.
- the numerical values of unit type, base material, unit area ratio, A before catalyst loading, sealing material layer type, sealing material layer area ratio, sealing material layer thickness, and B before catalyst loading in this experimental example 1 are summarized. These are shown in Table 3.
- the sealing material layer area ratio refers to the ratio of the total cross-sectional area of the sealing material layer 26 to the cross-sectional area of the her cam structure 20.
- a (gZcm 3 ) is the product of the apparent density of the honeycomb unit 10 and the volume ratio of the honeycomb unit 10 in the entire hammer cam structure 20, and is obtained by the following equation (2). It was.
- B (gZcm 3 ) is the product of the apparent density of the seal material layer 26 and the volume ratio of the seal material layer 26 in the whole hard cam structure 20, and was obtained by the following equation (3). .
- Table 3 also summarizes the contents related to Experimental Examples 2 to 24 described later.
- the specific surface area per unit volume of the resulting her cam structure 20 of Experimental Example 1 was 37400 m 2 / L, and the unit area ratio was 93.5%.
- the specific surface area per unit volume was determined by the following formula (4).
- Area area ⁇ The area ratio of the porous area to the total cross-sectional area of the porous ⁇ unit with respect to the cross-sectional area of the ⁇ -two cam structure.
- A: / 1 The volume density of the Nicam structure multiplied by the ratio of the volume occupied by the camut; the apparent density of the force unit; (; the apparent density of the camunit) X (unit area ratio ⁇ 00)
- Seal material layer area ratio Percentage of the total cross-sectional area of the seal material layer relative to the cross-sectional area of the cam structure
- the raw materials of the honeycomb unit 10 are mixed so that the blending amount shown in Table 1 is obtained, and the sealing material paste is prepared so that the blending amount shown in Table 2 is obtained, and the Hercom unit 10 and the sealing material shown in Table 3 are prepared.
- the hard cam structures 20 of Experimental Examples 2 to 23 were fabricated.
- a commercially available cordierite support having alumina as a catalyst support layer formed inside the through-hole was prepared.
- This cordierite carrier had a diameter of 135 mm, a length of 75 mm, a hexagonal shape of through-holes, a wall thickness of 0.18 mm, and a cell density of 60 Zcm 2 (400 cpsi).
- a 0.25 mol ZL platinum nitrate solution was prepared. This platinum nitrate aqueous solution was subjected to a pressure so that the amount of platinum supported was 5.
- OgZL in terms of platinum weight per unit volume of the Hercam structure. Water was absorbed in a carrier and calcined at 600 ° C for lh. In this way, the Hercam structure of Experimental Example 24 carrying the platinum catalyst was obtained.
- the specific surface area per unit volume of the obtained No-cam structure was 25 OOOm 2 ZL.
- the apparent densities of the her cams 1 to 5 as the her cam unit 10 and the sealing materials 1 to 4 as the sealing material layer 26 were measured.
- a of the two-cam unit 10 measures the dry weight Ga (g) of the her-cam unit 10 and the volume Va (cm 3 ) of the outer shape of the her-cam unit 10, and The volume ratio Y (%) occupied by the honeycomb unit 10 in the volume was obtained, and the force of the following formula (2) was also obtained.
- the wrinkles of the sealing material layer 26 are obtained by solidifying the sealing material paste into a cubic shape, and then cutting out into 1 cm squares, the dry weight Gb (g) of the cut sealing material layer 26, and the volume of the outer shape of the sealing material layer 26.
- Vb (cm 3 ) was measured, and the volume ratio Z (%) occupied by the sealing material layer 26 in the volume of the her cam structure 20 was determined from the following equation (3).
- the ratio ⁇ and the unit area ratio have the same value, and the ratio Z and The area ratio of the sealing material layer is the same value. Therefore, A can be obtained by (apparent density of the knove cam unit 10) X ((unit area ratio) / 100). Further, B can be obtained by (apparent density of sealing material layer) X ((seal material layer area ratio) Z100).
- the porosity of Experimental Examples 1 to 24 was measured. This measurement was performed by mercury porosimetry based on JIS-R1655 using Shimadzu Corporation automatic porosimeter Autopore III 9405 as a measuring instrument. Specifically, the Hercam unit 10 is cut into a cube of about 0.8 cm, ultrasonically cleaned with ion-exchanged water, dried, and then measured in the measuring range of 0.1 to 360 m using the above measuring instrument. did. In the range of 100 to 360 m, measurement was performed at a pressure of 0.1 lpsia, and in the range of 0.1 to 100 m, measurement was performed at a pressure of 0.25 psia.
- the specific surface area per unit volume of the hard cam structures of 1 to 24 was measured.
- the BET specific surface area M (m 2 / g) per unit weight of the Hercam unit 10 was measured.
- the BET specific surface area was measured by a one-point method using a BET measuring device (Micromeritics Flowsorb TM -2300, manufactured by Shimadzu Corporation) according to JIS-R-1626 (1996) defined by Japanese Industrial Standards.
- a sample cut into a cylindrical piece (diameter 15 mm x height 15 mm) was used.
- the apparent density N (g / L) of the her cam unit 10 was calculated from the weight of the her cam unit 10 and the volume of the outer shape.
- the apparent density N (g / L) of the hard cam unit 10 is the same value as the GaZVa X 1000 described above. Then, the unit area ratio was L (%), and the specific surface area C (mso L) per unit volume of Experimental Examples 1 to 24 was obtained from the following equation (4).
- the specific surface area of the her cam structure means the specific surface area per apparent volume of the her cam structure. Since the unit area ratio L (%) is the same as the volume ratio Y (%) occupied by the hard work 10 as described above, the expression (4) is the same as the expression (5). . In addition, the specific surface area per unit volume of the Hercam unit 10 was calculated by ⁇ ⁇ ⁇ . In this measurement, apparent density measurement, and porosity measurement, measurement was performed using the honeycomb unit 10 before supporting the catalyst (platinum).
- the purification rate of the exhaust gas of Experimental Examples 1 to 24 was measured. This measurement was performed using the exhaust gas purification measuring device 60 shown in FIG.
- the exhaust gas purification measuring device 60 includes an engine 30, a casing 38 in which the honeycomb structure 20 is fixed, a gas sampler 61 that samples exhaust gas before flowing through the hard cam structure 20, and a hard cam. Gas sampler 62 that samples exhaust gas after flowing through structure 20, gas analyzer 63 that analyzes the concentration of harmful substances contained in exhaust gas, and temperature measurement that measures the temperature of honeycomb structure 20 using a thermocouple 64.
- a casing 38 was connected to a hold 32 connected to the engine 30. Next, the measurement procedure will be described. First, exhaust gas from the engine 30 was circulated in the above-described Experimental Examples 1 to 24.
- the engine 30 was operated so that the cycle according to the 10-15 mode exhaust gas measurement method of a diesel vehicle was performed three times. Then, hydrocarbons (HC) and exhaust gas sampled by gas samplers 61 and 62 The concentration of carbon monoxide (CO) was measured by a gas analyzer 63.
- the purification rate is calculated from the following equation (5) using the concentration CO contained in the exhaust gas before flowing through the honeycomb structure 20 and the concentration contained in the exhaust gas after flowing through the hard structure 20 using Ci. Calculated.
- Table 4 shows the unit types, sealing material layer types, A, B, AZB, and NO-CAM structure 20 of the experimental examples 1 to 24, specific surface area C per unit volume, and HC and CO purifiers of the exhaust gas.
- Fig. 5 shows the units plotted for the experimental examples 1 to 24, where the horizontal axis is the specific surface area C per unit volume of the No-Cam structure 20 and the vertical axis is A / B. Ratio table per volume It is explanatory drawing showing the relationship between the area C and AZB.
- the values in the range of the above-described equation (1) are plotted as “O”, and those outside the range of the equation (1) are plotted as “ ⁇ ”, and the sample numbers of each experimental example are attached to each point.
- the sealing material layer 26 covering the outer surface 13 of the her cam unit 10 serves as a heat insulating material. It was speculated that the exhaust gas purification rate was improved because the temperature drop of the her cam structure 20 was suppressed.
- the present invention can be used, for example, to remove unnecessary substances contained in the fluid by flowing the fluid through the nozzle-cam structure or to convert a component contained in the fluid into another component.
- it can be used in various filter-related industries that purify gases and liquids.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Environmental & Geological Engineering (AREA)
- Composite Materials (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Biomedical Technology (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Catalysts (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Exhaust Gas After Treatment (AREA)
Abstract
ハニカム構造体20は、長手方向に沿って並列する複数の貫通孔12を有する2以上のハニカムユニット10と、ユニット10を貫通孔12が開口していない外面13で接合するシール材層26とを備えている。ハニカム構造体20は、ハニカムユニット10の見掛け密度と全体に占めるハニカムユニット10の体積割合との積をA(g/cm3)、シール材層26の見掛け密度と全体に占めるシール材層26の体積割合との積をB(g/cm3)、ハニカム構造体20の単位体積あたりの比表面積をC(m2/L)としたとき2≦A/B≦0.0002×C+5(28000≦C);式(1)を充足している。このため、ユニット10の外周を覆うシール材層26により温度を保持させて排ガスの浄化性能を高めることができる。
Description
明 細 書
ノヽニカム構造体
技術分野
[0001] 本発明は、ハ-カム構造体に関する。
背景技術
[0002] 従来、排ガス浄化に用いられる触媒担体として、活性アルミナなどの触媒担持層を ハ-カム構造体の貫通孔内部に設けたものが知られている。特に、排ガスと触媒との 接触確率を高めるために、ハニカム構造体のセル形状を六角形状や円形状としたり 、セル密度を 600〜1200セル Zinch2 (cpsi)とし、表面から深さ 100 m以内に存 在する部分が触媒担持層の体積の 80%以上になるようにしたものが知られている( 例えば、特開平 10— 263416号公報参照)。
発明の開示
[0003] し力しながら、上述した公報に記載されたハ-カム構造体では、排ガスとの接触確 率を高めるべくセル形状及びセル密度を工夫した力 それでも単位体積あたりの比 表面積は十分大きくなぐ触媒を十分高分散できないことがあった。また、ハ-カム構 造体の見掛け密度にっ 、ては考慮されて 、なかった。
[0004] 本発明は、このような課題に鑑みなされたものであり、ハ-カム構造体の見掛け密 度と比表面積とを好適な範囲とすることにより排ガスの浄ィ匕率を高めることができるハ 二カム構造体を提供することを目的とする。
[0005] 本発明は、上述の目的を達成するために以下の手段を採った。すなわち、本発明 のハニカム構造体は、
複数の貫通孔を有するハ-カムユニットと、 2以上の該ハ-カムユニットを該貫通孔 が開口して ヽな 、外面で接合するシール材層とを備えたノヽ-カム構造体であって、 前記ハニカムユニットの見掛け密度と前記ハニカム構造体の全体に占める前記ハ 二カムユニットの体積割合との積を A (gZcm3)、前記シール材層の見掛け密度と前 記ハ-カム構造体の全体に占める前記シール材層の体積割合との積を B (g/cm3) 、前記ハ-カム構造体の単位体積あたりの比表面積を C (m2/L)としたとき 2≤ A/
B≤0. 0002 X C + 5 (28000≤C)を満たすものである。
[0006] このハ-カム構造体は、ハ-カム構造体の全体のうちハ-カムユニットの占める見 掛け密度と、ハ-カム構造体の全体のうちシール材層の占める見掛け密度と、ハ-カ ム構造体の単位体積あたりの比表面積とを規定したものである。上述したように、一 般に、排ガスの浄ィ匕率を向上させるためには、排ガスとハ-カム構造体に担持された 触媒との接触確率を上げることが必要である。そのためには、触媒担体の比表面積 を向上させ、担持させる触媒の粒径を小さくして十分に高分散させることが有効であ る。触媒を高分散させたものは触媒の比表面積が高くなるため触媒の担持量が同じ であっても排ガスと触媒との接触確率が向上するためである。また、排ガスの浄化に おいて、触媒の活性温度以上になるようにハ-カム構造体の温度を保持することが 必要である。ここで、ハ-カムユニットの見掛け密度や、ノ、二カムユニットの外面に形 成されているシール材層の見掛け密度は、ハニカム構造体の暖まりやすさや冷めや すさなどに影響することが考えられる。本発明者らは、複数の貫通孔を有する 2以上 のハ-カムユニットを接合したハ-カム構造体にぉ 、て、ハ-カムユニット及びシー ル材層の見掛け密度と、ハ-カム構造体の比表面積との関係に着目し、鋭意研究し た結果、ハ-カムユニットの見掛け密度とハ-カム構造体の全体に占めるハ-カムュ ニットの体積割合との積を A (gZcm3)、シール材層の見掛け密度とハ-カム構造体 の全体に占めるシール材層の体積割合との積を B (g/cm3)、ハ-カム構造体の単 位体積あたりの比表面積を C (m2/L)としたとき 2≤ A/B≤0. 0002 X C + 5 (280 00≤C)を充足すると排ガスの浄ィ匕率を高めることができることを見出し、本発明を完 成するに至った。
[0007] 本発明のハ-カム構造体において、更に、前記比表面積 Cが 35000m2/L以上を 満たすことがより好ましぐ 38000m2/L以上を満たすことが最も好ましい。 C値が 35 OOOm2ZL以上では、一層触媒を高分散させることができる。また、更に、触媒の分 散の限界を考慮すると前記比表面積 Cが 70000m2/L以下を満たすことが好ましい
[0008] 本発明のハ-カム構造体において、更に、前記積 Aが 0. 2gZcm3以上 0. 5g/c m3以下を満たすことが好ましい。積 Aが 0. 2gZcm3未満では、ハ-カムユニットの強
度が弱くなることがあり、 0. 5gZcm3を超えるとハ-カム構造体の熱容量が大きくなり 触媒の活性温度になるまでに時間が力かることがある。
[0009] 本発明のハ-カム構造体において、前記シール材層の厚さが 0. 1〜 2. Ommであ ることが好ましい。この厚さが 0. 1mm未満では、ハ-カムユニット同士の十分な接合 強度が得られなくなることがあり、 2. Ommを超えると、触媒反応にあまり関係しない 部分であるシール材層の体積が相対的に大きくなるため、排ガスの浄ィ匕率の観点か らは好ましくない。
[0010] 本発明のハ-カム構造体において、前記ハ-カムユニットは、無機粒子及び無機 繊維を含んでなるものが好ましい。無機粒子としては、例えばアルミナ、シリカ、チタ 二了、ジルコユア、セリア、ムライト及びゼォライトなど力も選ばれる 1種又は 2種以上 の粒子が挙げられる。無機繊維としては、例えばアルミナ、シリカ、炭化珪素、シリカ アルミナ、ガラス、チタン酸カリウム及びホウ酸アルミニウムなど力 選ばれる 1種又は 2種以上の繊維ゃゥイス力が挙げられる。こうすれば、比表面積が高く且つ強度が高 ぃハ-カムユニットを比較的容易に作成できる。また、これにカ卩えて無機バインダを 含んで製造されることが好ましい。無機ノインダとしては、例えばアルミナゾル、シリカ ゾル、チタ-ァゾル及び水ガラスなど力 選ばれる 1種又は 2種以上のバインダが挙 げられる。こうすれば、低い焼成温度でも十分な強度を得ることが可能となる。
[0011]
、て、前記シール材層は、無機粒子及び無機繊維 を含んでなるものが好ましい。無機粒子としては、例えば上述したものや炭化珪素、 炭化ホウ素、窒化珪素など力 選ばれる 1種又は 2種以上の粒子が挙げられる。また 、無機繊維としては、例えば上述したものなど力 選ばれる 1種又は 2種以上の繊維 ゃゥイス力が挙げられる。また、これに加えて無機バインダを含んで製造されることが 好ましい。無機バインダとしては、例えば上述したものなど力 選ばれる 1種又は 2種 以上のバインダが挙げられる。こうすれば、ハ-カム構造体としての耐熱衝撃性を向 上させることができると共に、比較的容易に所望の見掛け密度のシール材層とするこ とがでさる。
[0012] 本発明のハ-カム構造体において、触媒が担持されてなることが好ましい。ここで、 触媒としては、排ガスに含まれる CO, HC, NOxなどを浄ィ匕するもの、例えば貴金属
やアルカリ金属やアルカリ土類金属などであってもよ 、し、酸化化合物などであって もよい。貴金属としては、例えば白金、ノラジウム及びロジウムなど力も選ばれる 1種 以上が挙げられ、アルカリ金属としては、例えばナトリウム及びカリウムなど力 選ば れる 1種以上が挙げられ、アルカリ土類金属としては、例えばマグネシウムやバリウム など力 選ばれる 1種以上が挙げられる。また、酸ィ匕化合物としては、例えばべ口ブス カイト構造を有するもの(LaCoO , LaMnOなど)及び CeOなど力も選ばれる 1種以
3 3 2
上が挙げられる。ぺロブスカイト構造を有する酸化化合物としては、例えばべ口ブス力 イト構造 (一般式 ABO )の Aサイトが La、 Y及び Ceなど力も選ばれる 1種以上の元素
3
であり、このうち Laが好ましぐ一般式の Bサイトが Fe、 Co、 Ni及び Mnなどから選ば れる 1種又は 2種以上の元素であるものなどが挙げられる。なお、 La K CoOな
0.75 0.25 3 どのように Aサイトの元素の一部を K、 Sr及び Agなどに置換してもよい。なお、触媒を 担持した本発明のハ-カム構造体は、車両の排ガス浄ィ匕に用いてもよい。
図面の簡単な説明
[0013] [図 1]本実施形態のハニカム構造体 20の説明図である。
[図 2]本実施形態のハニカムユニット 10の説明図であり、 (a)は斜視図、(b)は(a)の X— X断面図である。
[図 3]AZBとハ-カム構造体 20の単位体積あたりの比表面積 Cとの好適範囲である [図 4]排ガス浄ィ匕測定装置 60の説明図である。
[図 5]AZBと単位体積あたりの比表面積 Cとの関係を表す説明図である。
発明を実施するための最良の形態
[0014] 次に、本発明を実施するための最良の形態を図を用いて説明する。
[0015] まず、本実施形態のハニカム構造体について説明する。図 1は、本実施形態のハ 二カム構造体 20の説明図であり、図 2は、ハニカムユニット 10の説明図であり、(a)は 斜視図、(b)は(a)の X—X断面図である。このハ-カム構造体 20は、エンジンの排 ガス中の有害物質 (例えば、炭化水素 HC,—酸化炭素 CO,窒素酸化物 NOxなど) を浄ィ匕する機能を持つ触媒コンバータ用のハ-カム構造体として構成されている。こ のハ-カム構造体 20は、長手方向に沿って並列する複数の貫通孔 12を有する角柱
状に形成された 2以上のハ-カムユニット 10と、ハ-カムユニット 10を貫通孔 12が開 口して 、な 、外面 13で接合するシール材層 26と、シール材層 26で接合された 2以 上のハ-カムユニット 10のうち貫通孔 12が開口していない外周面を覆うコーティング 材層 27と、を備えたものである。
このハ-カム構造体 20は、ハ-カムユニット 10の見掛け密度とハ-カム構造体 20 の全体に占めるハ-カムユニット 10の体積割合との積を A (g/cm3)、シール材層 2 6の見掛け密度とハ-カム構造体 20の全体に占めるシール材層 26の体積割合との 積を B (g/cm3)、ハ-カム構造体 20の単位体積あたりの比表面積を C (m2/L)とし たとき 2≤AZB≤0. 0002 X C + 5 (28000≤ C);式(1)を充足している。ここで、 A は、ハ-カムユニット 10の見掛け密度(乾燥重量 Z体積)に、ハ-カム構造体 20の 全体の体積に対するハ-カムユニット 10の体積の割合を乗算したものである。この見 掛け密度を算出するために用いる体積は、気孔及び貫通孔 (セル)を含んだ体積と する。この Aは、 0. 2g/cm3≤A≤0. 5g/cm3を満たすことが好ましい。 Aが 0. 2g Zcm3未満では、ハ-カムユニットの強度が弱くなることがあり、 0. 5gZcm3を超える とハ-カム構造体の熱容量が大きくなり触媒の活性温度になるまで時間が力かること がある。また、 Bは、シール材層 26の見掛け密度(乾燥重量 Z体積)に、ノ、二カム構 造体 20の全体の体積に対するシール材層 26の体積の割合を乗算したものである。 単位体積あたりの比表面積 Cは、ハ-カムユニット 10の BET比表面積測定による単 位重量あたりの比表面積力 ハ-カムユニットの気孔及びセルを含む単位体積あた りの比表面積を算出し、ハ-カム構造体 20の全体積のうちハ-カムユニット 10の体 積の占める割合を乗算したものである。つまり、シール材層 26は排ガスの浄ィ匕にほと んど寄与しな 、部分であるため、このシール材層 26の体積を除外してハ-カム構造 体 20の体積あたりの比表面積を求めるのである。この比表面積 Cは、 28000m2/L 以上であることが必要であり、 35000m2ZL以上であることがより好ましぐ 38000m2 ZLであることが最も好ましい。また、更に、触媒の分散の限界を考慮すると単位体積 あたりの比表面積 Cが 70000m2ZL以下を満たすことが好ましい。図 3に、 Aと Bとの 比である AZBとハ-カム構造体 20の単位体積あたりの比表面積 Cとの好適範囲を 示す。この範囲に含まれるようにハ-カム構造体 20を作製すると、排ガスの浄化性能
を高めることができる。
[0017] ハ-カムユニット 10は、貫通孔 12に対して直交する面の断面が正方形に形成され ており、このハ-カムユニット 10を複数接合したノヽ-カム構造体 20は、外形が円柱状 に形成されている。なお、ハ-カムユニット 10の形状は、例えば貫通孔 12に対して直 交する面の断面が長方形や六角形や扇状のものであってもよいし、ハニカム構造体 20の形状は、例えば貫通孔 12に対して直交する面の断面が角柱状又は楕円柱状 のものであってもよい。
[0018] ハニカムユニット 10に形成される貫通孔 12は、断面が正方形に形成されている。な お、断面を三角形や六角形としてもよい。貫通孔 12同士の間の壁部 15の厚さ (壁厚 )【ま、0. 05〜0. 35mmの範囲力 S好ましく、 0. 10〜0. 30mm力 Sより好ましく、 0. 15 〜0. 25mmが最も好ましい。壁厚が 0. 05mm未満ではハ-カムユニット 10の強度 が低下し、 0. 35mmを超えると、排ガスと壁部 15の内部に担持された触媒との接触 が起きにくくなることがあるため、触媒性能が低下することがある。また、単位断面積 あたりの貫通孔の数(セル密度)は、 15. 5〜186個 Zcm2 (100〜1200cpsi)が好ま しく、 46. 5〜170. 5個 Zcm2 (300〜: L lOOcpsi)力 り好ましく、 62. 0〜155個 Zc m2 (400〜1000cpsi)が最も好ましい。貫通孔の数が 15. 5個 Zcm2未満では、ハニ カムユニット内部の排ガスと接触する壁の面積が小さくなり、 186個/ cm2を超えると 、圧力損失も高くなるし、ノ、二カムユニット 10の作製が困難になるためである。ハ-カ ムユニット 10の気孔率は、 30〜80%であることが好ましぐ 40〜70%であることが好 ましい。気孔率が 30%未満では、見掛け密度が大きくなることがあり、気孔率が 80% を超えると強度が低くなることがある。
[0019] ハ-カムユニット 10の大きさとしては、ユニットの断面積が 5〜50cm2で形成するの が好ましぐ 6〜40cm2で形成するのがより好ましぐ 8〜30cm2で形成することが最も 好ましい。この範囲では、ハ-カム構造体 20の単位体積あたりの比表面積を大きく 保つことができ、触媒を高分散させることが可能となるとともに、熱衝撃や振動などの 外力が加わってもハ-カム構造体としての形状を保持することができる。また、ハ-カ ム構造体 20の断面積に対するハ-カムユニット 10の総断面積の占める割合 (以下ュ ニット面積割合という)が 85%以上であることが好ましぐ 90%以上であることがより好
ましい。この割合が 85%未満では、触媒を担持する表面積が相対的に小さくなつたり 、圧力損失が大きくなつたりしてしまうため好ましくない。
[0020] ハ-カムユニット 10には、無機粒子としてのアルミナ粒子、無機繊維としてのホウ酸 アルミニウムウイスカ及び無機ノインダとしてのシリカゾルが含まれて製造されている
。なお、無機粒子としては、例えばシリカ、チタ二了、ジルコユア、セリア、ムライト及び ゼォライトなど力 選ばれる 1種又は 2種以上の粒子が含まれていてもよい。また、無 機繊維としては、例えばアルミナ、シリカ、炭化珪素、シリカアルミナ、ガラス及びチタ ン酸カリウムなどカゝら選ばれる 1種又は 2種以上の繊維ゃゥイス力が含まれていてもよ い。また、無機バインダとしては、例えばアルミナゾル、チタ-ァゾル及び水ガラスな ど力 選ばれる 1種又は 2種以上のバインダが含まれて 、てもよ 、。
[0021] シール材層 26には、無機粒子としての炭化珪素、無機繊維としてのアルミナ繊維 及び無機バインダとしてのシリカゾルが含まれている。なお、この無機粒子は、上述 のハ-カムユニット 10で説明したものや炭化ホウ素、窒化珪素など力も選ばれる 1種 又は 2種以上の粒子が含まれていてもよい。また、無機繊維及び無機バインダは、上 述のハ二カムユニット 10で説明したものの中力も選択してもよい。このシール材層 26 の気孔率は、 10〜80%であることが好ましぐ 15〜70%であることがより好ましい。 気孔率が 10%未満では、見掛け密度が大きくなり触媒活性温度に到達しに《なる ことがあり、気孔率が 80%を超えるとハ-カムユニット 10を接合する強度が低下する ため好ましくない。
[0022] ハ-カム構造体 20には、酸化触媒としての白金が壁部 15に直接担持されている。
触媒の担持量は、白金などの貴金属の場合、ハ-カム構造体 20の単位体積あたり の触媒の重量で、 l〜5gZLであることが好ましい。触媒の担持方法は、特に限定さ れないが、含浸法が比較的簡便であり好ましい。
[0023] 次に、本発明のハ-カム構造体 20の製造方法について各工程別に説明する。ここ では、アルミナを主成分としてハ-カム構造体 20を製造する方法にっ 、て説明する 。まず、無機粒子としてのアルミナ粒子、無機繊維としてのホウ酸アルミニウムウイスカ 及び無機バインダとしてのシリカゾルを混合して原料ペーストを調製する。なお、無機 粒子、無機繊維及び無機ノインダとしては、例えば上述のハ-カムユニット 10で説
明したものを用いてもよい。原料ペーストには、これらのほかに有機バインダ、分散媒 及び成形助剤を成形性にあわせて適宜加えてもよい。有機ノ インダとしては、例えば メチノレセノレロース、カノレボキシメチノレセノレロース、ヒドロキシェチノレセノレロース、ポリエ チレングリコール、フエノール榭脂及びエポキシ榭脂から選ばれる 1種以上の有機バ インダが挙げられる。有機バインダの配合量は、アルミナ粒子、ホウ酸アルミニウムゥ イス力及びシリカゾルの合計 100質量部に対して、 1〜: LO質量部が好ましい。分散媒 としては、例えば水、有機溶媒 (ベンゼンなど)及びアルコール (メタノールなど)など が挙げられる。成形助剤としては、例えばエチレングリコール、デキストリン、脂肪酸、 脂肪酸石酸及びポリアルコールなどが挙げられる。原料の混合は、ミキサーゃァトラ イタなどを用いてもよぐエーダーなどで十分に混練してもよい。原料ペーストを成型 する方法は、例えば押出成形などによって貫通孔を有するハニカム形状に成形する
[0024] 次に、得られた成形体を乾燥する。乾燥機は、例えばマイクロ波乾燥機、熱風乾燥 機などを用いる。また、有機バインダなどを添加したときには、脱脂することが好まし い。脱脂条件は、成形体に含まれる有機物の種類や量によって適宜選択するが、お およそ 400°C、 2hrが好ましい。次に、乾燥及び脱脂した成形体を 600〜1000°Cで 焼成する。焼成温度が 600°C未満では無機粒子などの焼結が進行せずノヽ-カム構 造体としての強度が低くなり、 1000°Cを超えると無機粒子などの焼結が進行しすぎ て比表面積が小さくなり、担持させる触媒を十分に高分散させることができなくなるこ とがあるためである。これらの工程を経て複数の貫通孔を有するハ-カムユニット 10 を得る。
[0025] 次に、得られたハ-カムユニット 10にシール材層となるシール材ペーストを塗布し てハニカムユニット 10を順次接合させ、その後乾燥'固化させて、シール材層 26を形 成しノヽ-カムユニット接合体を作製する。シール材ペーストは、無機粒子としての炭 化珪素粒子、無機繊維としてのアルミナ繊維及び無機バインダとしてのシリカゾルを 混合して調製する。ここで、シール材ペーストは、例えば無機バインダと無機粒子とを 混ぜたものや、無機バインダと無機繊維とを混ぜたものや、無機バインダと無機粒子 と無機繊維とを混ぜたものなどを用いることができる。なお、無機粒子、無機繊維及
び無機バインダとしては、例えば上述のシール材層 26で説明したものを用いてもよ い。また、シール材ペーストに有機バインダを加えてもよい。有機バインダとしては、 例えばポリビュルアルコール、メチルセルロース、ェチルセルロース及びカルボキシメ チルセルロースなど力も選ばれる 1種以上の有機バインダが挙げられる。このシール 材ペーストは、シール材ペーストの固化後に上述の式(1)の範囲を満たすように適宜 調製する。ハ-カムユニット 10を接合させるシール材層の厚さは、 0. 1〜2. Ommが 好ましい。シール材層の厚さが 0. 1mm未満では十分な接合強度が得られないため 好ましくない。また、 2. Ommを超えるとハ-カム構造体の単位体積あたりの比表面 積が低下するため好ましくない。これは、シール材層は触媒担体としてあまり機能し ない部分だ力もである。なお、接合させるハ-カムユニット 10の数は、使用するハ- カム構造体 20の大きさに合わせて適宜決めればよい。次に、ノ、二カムユニット接合 体をノ、二カム構造体 20の大きさとなるように適宜切断'研磨などを行い、貫通孔が開 口して 、な 、外周面 (側面)にコーティング材ペーストを塗布して乾燥'固化させてコ 一ティング材層 27を形成させる。こうすれば、外周面を保護して強度を高めることが できる。コーティング材ペーストは、シール材と同様の組成及び配合比としてもよいし 、異なる組成及び配合比としてもよい。コーティング材層の厚みは、 0. l〜2mmであ ることが好ましい。そして、この接合体を仮焼してハ-カム担体 (触媒を担持する前の ハ-カム構造体をいう)とする。仮焼する条件は、含まれる有機物の種類や量によつ て適宜決める力 おおよそ 700°Cで 2hrが好まし!/、。
続、て、得られたノヽ-カム担体に触媒を担持させる。ここでは、酸化触媒としての白 金を担持する。まず、触媒を含む溶液を調製し、この溶液にハニカム担体を浸漬した のち、引き上げ、貫通孔 12などに残った余分な溶液を吸引によって取り除く。そして 、 80〜200°Cで乾燥させ、 500〜700°Cで焼成を行うことにより触媒が担持されたノヽ 二カム構造体 20を得ることができる。また、数種類の触媒を担持させるときには、ハニ カム担体を触媒の溶液に浸漬させ焼成する工程をそれぞれの触媒について繰り返し 行ってもよい。触媒の担持量は、その種類や組み合わせなどにより適宜選択する。な お、触媒の担持は、ハ-カム担体を作製した後に行ってもよいし、原料の無機粒子の 段階で行ってもよいし、ハ-カムユニット 10を作製した段階で行ってもよい。
[0027] 以上詳述した本実施形態のハ-カム構造体 20によれば、 2≤AZB≤0. 0002 X C + 5 (28000≤C)を充足しているため、排ガスの浄化率を高めることができる。また 、シール材層の厚さを 0. 1〜2. Ommとすることで、ハ-カムユニット同士の十分な接 合強度が得られると共に、触媒反応にあまり関係しない部分を低減させて排ガスの浄 化率を高めることができる。
[0028] なお、本発明は上述した実施形態に何ら限定されることはなぐ本発明の技術的範 囲に属する限り種々の態様で実施し得ることはいうまでもない。
実施例
[0029] 以下には、ハ-カム構造体 20を具体的に製造した例を、実験例として説明する。
[0030] [実験例 1]
まず、 Ίアルミナ粒子 (住友ィ匕学社製 KC— 501,平均粒径 1 μ m) 2250質量部、 ホウ酸アルミニウムウイスカ(平均繊維長 20 μ m、平均繊維径 0. 5 m) 680質量部 、無機ノインダとしてのシリカゾル(固体濃度 30重量0 /0) 2600質量部、有機バインダ としてのメチルセルロース(MC) 320質量部、水、可塑剤(グリセリン)及び潤滑剤(商 品名ュニループ;日本油脂 (株) )を適量加えて混合 ·混練して混合組成物を得た。 次に、この混合組成物を長手方向に沿って並列する複数の貫通孔が形成された角 柱状に押出成形機により押出成形を行い、生の成形体を得た。そして、マイクロ波乾 燥機及び熱風乾燥機を用いて生の成形体を十分乾燥させ、 400°Cで 2h保持して脱 脂した。その後、 800°Cで 2h保持して焼成を行い、角柱状(34. 3mm X 34. 3mm X 75mm)、セル密度が 93個 Zcm2 (600cpsi)、壁厚が 0. 2mm、セル形状が正方 形のハ-カムユニット 10 (以下このサンプルをノヽ-カム 1とする)を得た。このハ-カム 1の構成材料 (基材)、シリカゾル及びメチルセルロースなどの配合量、焼成温度など の数値をまとめたものを表 1に示す。この表 1には、サンプルの測定結果としての見掛 け密度、気孔率及び単位体積あたりの比表面積などの数値も示し、後述するハ-カ ム 2〜5に関する内容もまとめて示す。得られたノヽ-カム 1の見掛け密度は 0. 45g/ cm3であり、気孔率は 60%であり、単位体積あたりの比表面積は 40000m2ZLであ つた。なお、見掛け密度、気孔率及び単位体積あたりの比表面積の算出方法は後述 する。
[0031] [表 1] τアルミナ チタニア シリカ 本ゥ酸: Γルミ シリカ メチル 焼成 見掛け 気孔 比表 径 配合量 径 配合量 径 配合量 - ソ'ル tA -x 温度 密度 率 面積
At m g μ- m g rn g g g g °c g/cm3 % n7L
'、二カム 1 1 2250 680 2600 320 800 0. 45 60 40000
/、:カム 2 2 2250 680 2600 320 800 0. 50 60 38000
/、:カム 3 2 2250 680 2600 320 850 0. 3Z 60 30000
/、二カム 4 1 1 500 2 750 680 2600 320 800 0. 40 60 42000
/、二カム 5 1 2250 680 2600 320 1 000 0. 45 60 28000
1 ) Λ二カム】〜 5は全て壁厚 0. 2IM, セル密度 600cps i, 開口率 65. 1 %である。
2 ) Λ二カム1…実験例 〜 8, Λ二 M2…実験例 9〜12, Λ二カム 3…実験例 1 3〜1 7,
Λ二カム小 ·■実験例 18〜21, Λ二カム 5…実験例 22〜23
[0032] 次に、炭化珪素粒子 (平均粒径 0. 5 m) 3600質量部、アルミナ繊維 (平均繊維 径 10 /ζ πι、平均繊維長 100 m、アスペクト比 10) 5500質量部、無機バインダとし てのシリカゾル(固体濃度 30重量0 /0) 3000質量部、有機バインダとしてのカルボキシ メチルセルロース(CMC) 50質量部及び水を適量混合しシール材ペースト(これをシ ール材 1とする)を調製した。このシール材 1の構成材料、シリカゾル、 CMCなどの配 合量、などの数値をまとめたものを表 2に示す。この表 2には、シール材の評価結果と しての固化後の見掛け密度及び気孔率の測定結果も示し、更に、後述するハニカム 2〜5に関する内容もまとめて示す。このシール材ペーストの厚さが lmmになるように ハ-カム 1の外面 13に塗布してハ-カムユニット 10を縦 4個、横 4個接合させ、接合 体を得た。そして、この接合体の正面が略点対称になるように円柱状にダイヤモンド カッターを用いて切断し、貫通孔を有しない円形の外表面に上述のシール材ペース トを 0. 5mm厚となるように塗布し外周面にコーティング材層 27を形成した。その後、 120°Cで乾燥を行 、、 700°Cで 2h保持してシール材層 26及びコーティング材層 27 の脱脂を行 、、円柱状(直径 135mm X高さ 75mm)のハニカム担体を得た。
[0033] [表 2]
S i C アルミナ アルミナ 本ゥ酸アルミ シリカ',ル CMC 見掛け 気孔率 径 配合量 径 配合量 繊維 二ゥムゥイス力 密度
^ m g m g g g g g g/cn3 % シ'ール材 1 0. 5 3600 5500 3000 50 1. 82 45 シ'ール材 2 0. 5 3600 5500 3000 50 1. 93 45 ン'ール材 3 0. 5 8000 1 100 3000 50 2. 72 1 5 シ'ール材 4 0. 5 1100 8000 3000 50 0. 87 70
¾ί シ -Λ材 1…実験例 1 ~5, 9, 14, 16, 18, 22, シ -Λ材 2…実験例 6, 1 0, 1 5, 20,
シ -Λ材 3 -実験例 7, 12, 13, 21 , シ -ル材 4…実験例 8, 11, 17, 1 9, 23 続いて、得られたノヽ-カム担体に白金を担持した。 0. 25molZLの硝酸白金溶液
を調製した。白金の担持量がハ-カム構造体の単位体積当たりの白金の重量で 5. OgZLとなるようにこの硝酸白金水溶液をノヽ-カム担体に吸水させ、 600°Cで lh焼 成した。こうして図 1に示す触媒を担持したノ、二カム構造体 20 (実験例 1)を得た。こ の実験例 1のユニット種類、基材、ユニット面積割合、触媒担持前の A、シール材層 種類、シール材層面積割合、シール材層厚さ及び触媒担持前の Bの各数値をまとめ たものを表 3に示す。ここで、シール材層面積割合とは、ハ-カム構造体 20の断面積 に対するシール材層 26の総断面積の占める割合をいう。また、 A(gZcm3)は、ハニ カムユニット 10の見掛け密度とハ-カム構造体 20の全体に占めるハ-カムユニット 1 0の体積割合との積をいい、後述の式(2)により求めた。また、 B (gZcm3)は、シー ル材層 26の見掛け密度とハ-カム構造体 20の全体に占めるシール材層 26の体積 割合との積をいい、後述の式(3)により求めた。なお、表 3には、後述する実験例 2〜 24に関する内容もまとめて示す。得られた実験例 1のハ-カム構造体 20の単位体積 当たりの比表面積は 37400m2/Lであり、ユニット面積割合は 93. 5%であった。な お、単位体積当たりの比表面積は、後述の式 (4)により求めた。
[表 3]
ユニット 基材 ュ二'; " A 2' シ -ル材層 シ-ル材 3 ) シ-ル材 Β 4 ) 面積 層面積 層厚さ
割合 割合
% g/cm3 % ■ g/cn3 実験例 1 ハニカム 1 τアルミナ 93. 5 0. 42 シ-ル材 1 6. 5 1. G 0. 1 2 実験例 2 Λ二カム 1 τアルミナ 89. 0 0. 40 シ -ル材 1 1 1. 0 1. 7 0. 20 実験例 3 '、二カム 1 τアル 98. 0 0. 44 シ-ル材 1 2. 0 0. 3 0. 04 実験例 4 Λ二カム 1 τアルミナ 87. 0 0. 39 シ -ル材 1 13. 0 2. 0 0. 24 実験例 5 ハニカム 1 τアルミナ 98- 5 0- 44 シ-ル材 1 1. 5 0. 2 0. 03 実験例 6 二カム〗 Tアルミナ 95- 0 0- 43 V-ル材 2 5. 0 0. 8 0. 1 0 実験例 7 ハニカム 1 T 7ルミナ 97- 0 0. 44 シ-ル材 3 3. 0 0. 5 0. 08 実験例 8 ハニカム1 τ 7Λミナ 96. 5 0. 43 シ-ル材 4 3. 5 0. 5 0. 03 実験例 9 ハニカム 2 チタ二 7 93. 5 0. 47 シ-ル材 1 6 5 1. 0 0. 1 2 実験例 10 ハニカム 2 チタ二 7 97. 0 0. 49 シ -ル材 2 3. 0 0. 5 0. 06 実験例 1 1 Λ二カム 2 チタニ7 95. 0 0. 48 シ_ル 4 5. 0 0. 8 0. 04 実験例 12 ハニカム 2 チタ二 7 97. 0 0. 49 シ-ル材 3 3. 0 0. 5 0. 08 実験例 13 ハニ Μ 3 シリカ 93. 5 0. 30 シ-ル材 3 6. 5 1. 0 0. 18 実験例 14 ハニカム 3 シリカ 98. 5 0. 32 シール本才 1 1. 5 0. 2 0. 03 実験例 15 ハニカム 3 シリカ 98. 5 0. 32 シ-ル材 2 1. 5 0. 2 0. 03 実験例 16 ハニカム 3 シリカ 93. 5 0. 30 シ-ル材 1 6. 5 1. 0 0. 1 2 実験例 17 ハニカム 3 シリカ 95. 0 0. 30 シール 4 5. 0 0. 8 0. 04 実験例 18 Λ二カム 4ァァ Αϊ +シリカ 93. 5 0— 37 シ-ル材 1 6. 5 1 0 0. 1 2 実験例 19 ハニカム 4 τアルミナ +シリカ 97. 0 0. 39 シ一ル $ί 4 3. 0 0. 5 0. 03 実験例 20 ハニカム 4 τアルミナ +シリカ 90. 0 0. 36 シ-ル材 2 1 0. 0 1. 5 0. 1 9 実験例 21 ハニカム 4 τ 7Λミナ +シリカ 98. 5 0. 39 シ-ル材 3 1. 5 0. 2 0. 04 実験例 22 ハニカム 5 τ ミナ 93- 5 0- 42 シ -ル材 1 6 5 1. 0 0. 1 2 実験例 23 ハニカム 5 Ύ 7Μ1 93. 5 0. 42 シ一ルお 4 6. 5 1. 0 0. 06 実験例リ 2"4 ココ --シン' 1Iラフ仆卄 - - ―- ―— ―一 ―- -
1 ) ] ト面積割 : Λ二カム構造体の断面積に対する多孔質 Λニ^ュニットの総断面積の占める T§ なおュニッ ト面積割合は気孔及びセルを含んで算出した値である
2 ) A : /1ニカム構造体の体積のうち;にカム ットの占める体積の割合を乗じた 力ムュニットの見掛け 密度 ; (;にカムュニットの見掛け密度) X (ユニット面積割合 Ί 00) から算出
3 ) シ-ル材層面積割合: /にカム構造体の断面積に対するシ -ル材層の総断面積の占める割合
4 ) B : /にカム構造体の体積のうちシ -Λ材層の占める体積の割合を乗じた-; 材層の見掛け密 度; (シ -Λ材層の見掛け密度 1 X (シ -Λ材層面積割合/ Ί 00) から算出
[0036] [実験例 2〜23]
表 1に示す配合量になるようにハニカムユニット 10の原料を混合し、表 2に示す配 合量になるようにシール材ペーストを調製し、表 3に示すハ-カムユニット 10とシール 材との組み合わせ、ユニット面積割合、シール材面積割合及びシール材層厚さに設 計したほかは実験例 1と同様にして実験例 2〜23のハ-カム構造体 20を作製した。
[0037] [実験例 24]
貫通孔内部に触媒担持層であるアルミナが形成してある市販のコージエライト担体 を用意した。このコージエライト担体は、直径 135mm、長さ 75mm、貫通孔の形状が 6角形であり、壁部の厚さ 0. 18mm,セル密度 60個 Zcm2 (400cpsi)であった。次 に、 0. 25molZLの硝酸白金溶液を調製した。白金の担持量がハ-カム構造体の 単位体積当たりの白金の重量で 5. OgZLとなるようにこの硝酸白金水溶液をノヽ-力
ム担体に吸水させ、 600°Cで lh焼成した。こうして白金触媒を担持した実験例 24の ハ-カム構造体を得た。得られたノヽ-カム構造体の単位体積あたりの比表面積は 25 OOOm2ZLであった。
[0038] [見掛け密度測定]
ハ-カムユニット 10としてのハ-カム 1〜5及びシール材層 26としてのシール材 1〜 4の見掛け密度測定を行った。ノ、二カムユニット 10の Aは、ハ-カムユニット 10の乾 燥重量 Ga (g)及びノヽ-カムユニット 10の外形の体積 Va (cm3)を測定し、ノヽ-カム構 造体 20の体積のうちハニカムユニット 10の占める体積割合 Y(%)を求めて次式(2) 力も求めた。また、シール材層 26の Βは、シール材ペーストを立方体状に固化させた のち、 1cm角に切り出し、該切り出したシール材層 26の乾燥重量 Gb (g)、シール材 層 26の外形の体積 Vb (cm3)を測定し、ハ-カム構造体 20の体積のうちシール材層 26の占める体積割合 Z (%)を求めて次式(3)から求めた。なお、ハ-カムユニット 10 とシール材層 26とのハ-カム構造体 20の軸方向の長さが同じであるため、上記割合 γとユニット面積割合とが同じ値になり、上記割合 Zとシール材層面積割合とが同じ値 になる。したがって、 Aは、(ノヽ二カムユニット 10の見掛け密度) X ( (ユニット面積割合 ) /100)により求めることができる。また、 Bは、(シール材層の見掛け密度) X ( (シ一 ル材層面積割合) Z100)により求めることができる。
A(g/cm3) = (Ga/Va) X (YZlOO)…式(2)
B (g/cm3) = (Gb/Vb) X (ZZlOO)…式(3)
[0039] [気孔率測定]
実験例 1〜24の気孔率測定を行った。この測定は、測定器として (株)島津製作所 社製自動ポロシメータ オートポア III 9405を用いて JIS—R1655に基づいて水銀圧 入法により行った。具体的には、ハ-カムユニット 10を 0. 8cm程度の立方体に切断 し、イオン交換水で超音波洗浄し乾燥したのち上記測定器を用いて、 0. 1〜360 mの測定範囲で測定した。 100〜360 mの範囲では、 0. lpsiaの圧力ごとに測定 し、 0. 1〜100 mの範囲では、 0. 25psiaの圧力ごとに測定した。
[0040] [単位体積当たりの比表面積測定]
実験例 1〜24のハ-カム構造体の単位体積あたりの比表面積測定を行った。まず
ハ-カムユニット 10の単位重量あたりの BET比表面積 M (m2/g)を測定した。 BET 比表面積は、BET測定装置(島津製作所製MicromeriticsフローソーブΠ— 2300)を 用いて、 日本工業規格で定められる JIS—R— 1626 (1996)に準じて 1点法により測 定した。測定には、円柱形状の小片(直径 15mm X高さ 15mm)に切り出したサンプ ルを用いた。次に、ハ-カムユニット 10の見掛け密度 N (g/L)をハ-カムユニット 10 の重量と外形の体積とから計算した。なお、このハ-カムユニット 10の見掛け密度 N ( g/L)は上述した GaZVa X 1000と同じ値である。そして、ユニット面積割合を L (% )とし、実験例 1〜24の単位体積当たりの比表面積 C (mソ L)を、次式 (4)から求め た。ここでのハ-カム構造体の比表面積は、ハ-カム構造体の見掛け体積あたりの 比表面積のことをいう。このユニット面積割合 L (%)は、上述したようにハ-カムュ-ッ ト 10の占める体積割合 Y(%)と同じであることから、式 (4)は、式(5)と同じである。ま た、ハ-カムユニット 10の単位体積あたりの比表面積は、 Μ Χ Νにより算出した。な お、この測定や見掛け密度測定や気孔率測定では、触媒(白金)を担持する前のハ 二カムユニット 10を用いて測定を行った。
比表面積 C (m2ZL) = (L/100) X M X N ;式(4)
比表面積じ(11127 = (¥7100) X M X (GaZVa X lOOO) N;式(5)
ガスの浄化率測定]
実験例 1〜24の排ガスの浄ィ匕率測定を行った。この測定は、図 4に示した排ガス浄 化測定装置 60を用いて行った。排ガス浄ィ匕測定装置 60は、エンジン 30と、ハニカム 構造体 20を内部に固定したケーシング 38と、ハ-カム構造体 20を流通する前の排 ガスをサンプリングするガスサンプラー 61と、ハ-カム構造体 20を流通した後の排ガ スをサンプリングするガスサンプラー 62と、排ガスに含まれる有害物質の濃度を分析 するガス分析計 63と、熱電対によりハニカム構造体 20の温度を測定する温度測定 器 64とにより構成されている。エンジン 30に接続されたマ-ホールド 32にケーシング 38を接続した。次に、測定手順を説明する。まず、上述した実験例 1〜24にエンジン 30からの排ガスを流通させた。この測定では、ディーゼル自動車の 10· 15モード排 出ガス測定方法に準じたサイクルを 3回行うようにエンジン 30を運転した。そして、ガ スサンプラー 61, 62によってサンプリングされた排ガスに含まれる炭化水素 (HC)及
び一酸ィ匕炭素(CO)の濃度をガス分析計 63によって測定した。浄化率は、ハニカム 構造体 20を流通する前の排ガスに含まれる濃度 COと、ハ-カム構造体 20を流通し た後の排ガスに含まれる濃度を Ciとを用いて次式(5)より計算した。
浄化率(%) = (CO— Ci) ZC0 X 100 ;式(5)
[0042] [実験結果]
表 4は、実験例 1〜24のユニット種類、シール材層種類、 A、 B、 AZB、 ノヽ-カム構 造体 20の単位体積あたりの比表面積 C、排ガスのうち HC及び COの浄ィ匕率などをま とめたものであり、図 5は、実験例 1〜24について、横軸をノヽ-カム構造体 20の単位 体積あたりの比表面積 Cとし、縦軸を A/Bとしてプロットした単位体積あたりの比表 面積 Cと AZBとの関係を表す説明図である。なお、図 5では、上述した式(1)の範囲 にあるものを〇、式(1)の範囲外のものを△としてプロットし、各実験例のサンプル番 号を各点に付した。表 4及び図 5から明らかなように、実験例 1〜3, 6〜7, 9〜12, 1 5-18, 21のサンプル、つまり、図 3の好適範囲(式(1)を満たす範囲)に入るサンプ ルでは、 HC及び COの浄化率が 80%以上であり、排ガスの浄化率が高かった。また 、比表面積 Cが 35000m2/L以上ではより浄ィ匕率が高くなる傾向を示した。この理由 としては比表面積 Cが大きくなると触媒の分散性が向上するため、排ガスの浄ィ匕率が 向上したものと考えられる。ここで、好適範囲である 2≤AZB≤0. 0002 X C + 5 (28 000≤C)を満たすときには、ハ-カムユニット 10の外面 13を覆っているシール材層 26が保温材の役割を果たし、ハ-カム構造体 20の降温が抑制されるため、排ガスの 浄ィ匕率が向上するものと推測された。
[0043] [表 4]
ユニット シ- -ル材層 A 1 * B 2' 構造体 3 ) 浄化率
の比表
¾ C HC CO g/cm3 g/ cm3 m7L % % 実験例 1 'にカム 1 シ- -ル材 1 0. 42 0. 12 3. 6 37400 91 96 実験例 2 '、二カム 1 シ. -ル材 1 0. 40 0. 20 2. 0 35600 89 95 実験例 3 Λ二カム 1 シ- -ル材 1 0. 44 0. 04 12. 1 39200 91 96 実験例 4 Λ二カム 1 シ- -ル材 1 0. 39 0. 24 1. 7 34800 72 76 実験例 5 Λ二カム 1 シ- -ル材 1 0. 44 0. 03 16. 2 39400 68 74 実験例 6 '、二カム 1 シ- -ル材 2 0. 43 0. 10 4. 4 38000 86 92 実験例 7 Λ二カム 1 シ- -ル材 3 0. 44 0. 08 5. 3 38800 87 92 実験例 8 Λ二カム 1 シ- -ル材 4 0. 43 0. 03 14. 3 38600 71 75 実験例 9 Λ二カム 2 リ ' - -ル材 1 0. 47 0. 12 4. 0 35530 83 89 実験例 10 Λ:カム 2 シ- -ル材 2 0. 49 0. 06 8. 4 36860 84 89 実験例 11 Λ二カム 2 シ- -ル材 4 0. 48 0. 04 10. 9 36100 86 90 実験例 12 ハニカム 2 シ- -ル材 3 0. 49 0. 08 5. 9 36860 86 89 実験例 13 Λ二カム 3 シ- -ル材 3 0. 30 0. 1 8 1. 7 28050 73 76 実験例 14 Λ二カム 3 'メ-ル材 1 0. 32 0. 03 1 1. 5 29550 70 76 実験例 15 ハニカム 3 ジ- -ル材 2 0. 32 0. 03 10. 9 29550 83 86 実験例 16 Λ二カム 3 -ノ- -ル材 1 0. 30 0. 1 2 2. 5 28050 85 91 実験例 17 ニカム 3 シ- -ル材 4 0. 30 0. 04 7. 0 28500 83 86 実験例 18 Λ二カム 4 シ- -ル材 1 0. 37 0. 12 3. 2 39270 92 97 実験例 19 Λ二カム 4 シ- -ル材 4 0. 39 0. 03 14. 9 40740 71 73 実験例 20 Λ:カム 4 シ-ル材 2 0. 36 0. 1 9 1. 9 37800 70 75 実験例 21 Λ:カム 4 シ- -ル材 3 0. 39 0. 04 9. 7 41370 90 94 実験例 22 Λ二カム 5 シ- -ル材 1 0. 42 0. 12 3. 6 26180 77 79 実験例 23 八二カム 5 シ- -ル材 4 0. 42 0. 06 7. 4 26180 78 79 実験例 24 コ-シ'エラ仆 ― 一 ― 一 25000 67 72
) A : /にカム構造体の体積のうち/にカム;!ニットの占める体積の割合を乗じた Λ=カム ュニットの見掛け密度; (Λ::カム ' の見掛け密度) X (ュニクト面積割合ノ100)
2 ) Β : /じカム構造体の体積のうちシ -ル材層の占める体積の割合を乗じたシ-ル材 層の見掛け密度; (シ -ル材層の見掛け密度) X (シ-ル材層面積割合/ 00)
3 ) Λ::カム構造体の単位体積あたリの比表面積 産業上の利用の可能性
本発明は、例えばノヽ-カム構造体に流体を流通させることによりその流体に含まれ る不要物を除去したり流体に含まれる成分を別の成分に変換したりするのに利用す ることができ、具体的には気体や液体を浄ィ匕する各種のフィルタ関連産業において 禾 IJ用することがでさる。
Claims
[1] 複数の貫通孔を有するハ-カムユニットと、 2以上の該ハ-カムユニットを該貫通孔が 開口して 、な 、外面で接合するシール材層とを備えたノヽ-カム構造体であって、 前記ハニカムユニットの見掛け密度と前記ハニカム構造体の全体に占める前記ハ 二カムユニットの体積割合との積を A (g/cm3)、前記シール材層の見掛け密度と前 記ハ-カム構造体の全体に占める前記シール材層の体積割合との積を B (g/cm3) 、前記ハ-カム構造体の単位体積あたりの比表面積を C (m2/L)としたとき 2≤ A/ B≤0. 0002 X C + 5 (28000≤C)を満たす、
ハニカム構造体。
[2] 前記比表面積 Cが 35000以上を満たす、
請求項 1に記載のハニカム構造体。
[3] 前記比表面積 Cが 70000以下を満たす、
請求項 1又は 2に記載のハ-カム構造体。
[4] 前記積 Aが 0. 2以上 0. 5以下を満たす、
請求項 1〜3のいずれかに記載のハ-カム構造体。
[5] 前記シール材層の厚さが 0. 1〜2. Ommである、
請求項 1〜4のいずれかに記載のハ-カム構造体。
[6] 前記ハ-カムユニットは、無機粒子及び無機繊維を含み、
前記シール材層は、前記ハ-カムユニットに含まれる無機粒子と同じか又は異なる 無機粒子及び前記ハ-カムユニットに含まれる無機繊維と同じか又は異なる無機繊 維を含む、
請求項 1〜5のいずれかに記載のハ-カム構造体。
[7] 排ガスを浄ィ匕可能な触媒が担持されてなる、
請求項 1〜6のいずれかに記載のハ-カム構造体。
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007523349A JP5042827B2 (ja) | 2005-06-29 | 2006-04-14 | ハニカム構造体 |
EP06013270.1A EP1752203B1 (en) | 2005-06-29 | 2006-06-27 | Honeycomb structure |
US11/475,967 US7794815B2 (en) | 2005-06-29 | 2006-06-28 | Honeycomb structure |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005190343 | 2005-06-29 | ||
JP2005-190343 | 2005-06-29 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/475,967 Continuation US7794815B2 (en) | 2005-06-29 | 2006-06-28 | Honeycomb structure |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2007000847A1 true WO2007000847A1 (ja) | 2007-01-04 |
Family
ID=37590371
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2006/307955 WO2007000847A1 (ja) | 2005-06-29 | 2006-04-14 | ハニカム構造体 |
Country Status (6)
Country | Link |
---|---|
US (1) | US7794815B2 (ja) |
EP (1) | EP1752203B1 (ja) |
JP (1) | JP5042827B2 (ja) |
KR (1) | KR100891892B1 (ja) |
CN (1) | CN100574882C (ja) |
WO (1) | WO2007000847A1 (ja) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008126328A1 (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 |
JP2016061532A (ja) * | 2014-09-19 | 2016-04-25 | 日本碍子株式会社 | 熱・音波変換部品および熱・音波変換ユニット |
JP2016187806A (ja) * | 2011-02-28 | 2016-11-04 | コーニング インコーポレイテッド | 二酸化炭素を捕捉するための物品 |
CN106536883A (zh) * | 2014-07-25 | 2017-03-22 | 曼柴油机和涡轮机欧洲股份公司 | 催化器装置和废气催化器 |
JPWO2018221692A1 (ja) * | 2017-05-31 | 2020-05-28 | 国立大学法人北海道大学 | 機能性構造体及び機能性構造体の製造方法 |
US11648538B2 (en) | 2017-05-31 | 2023-05-16 | National University Corporation Hokkaido University | Functional structural body and method for making functional structural body |
US11648542B2 (en) | 2017-05-31 | 2023-05-16 | National University Corporation Hokkaido University | Functional structural body and method for making functional structural body |
US11655157B2 (en) | 2017-05-31 | 2023-05-23 | National University Corporation Hokkaido University | Functional structural body and method for making functional structural body |
US11654422B2 (en) | 2017-05-31 | 2023-05-23 | Furukawa Electric Co., Ltd. | Structured catalyst for catalytic cracking or hydrodesulfurization, catalytic cracking apparatus and hydrodesulfurization apparatus including the structured catalyst, and method for producing structured catalyst for catalytic cracking or hydrodesulfurization |
US11666894B2 (en) | 2017-05-31 | 2023-06-06 | Furukawa Electric Co., Ltd. | Structured catalyst for CO shift or reverse shift and method for producing same, CO shift or reverse shift reactor, method for producing carbon dioxide and hydrogen, and method for producing carbon monoxide and water |
US11680211B2 (en) | 2017-05-31 | 2023-06-20 | Furukawa Electric Co., Ltd. | Structured catalyst for hydrodesulfurization, hydrodesulfurization device including the structured catalyst, and method for producing structured catalyst for hydrodesulfurization |
US11684909B2 (en) | 2017-05-31 | 2023-06-27 | Furukawa Electric Co., Ltd. | Structured catalyst for methanol reforming, methanol reforming device, method for producing structured catalyst for methanol reforming, and method for producing at least one of olefin or aromatic hydrocarbon |
US11904306B2 (en) | 2017-05-31 | 2024-02-20 | Furukawa Electric Co., Ltd. | Catalyst structure and method for producing the catalyst structure |
US12030041B2 (en) | 2017-05-31 | 2024-07-09 | Furukawa Electric Co., Ltd. | Structured catalyst for steam reforming, reforming apparatus provided with structured catalyst for steam reforming, and method for manufacturing structured catalyst for steam reforming |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4815108B2 (ja) * | 2003-12-26 | 2011-11-16 | イビデン株式会社 | ハニカム構造体 |
JP4527412B2 (ja) * | 2004-02-04 | 2010-08-18 | イビデン株式会社 | ハニカム構造体集合体及びハニカム触媒 |
ATE434716T1 (de) * | 2004-08-31 | 2009-07-15 | Ibiden Co Ltd | Abgasreinigungssystem |
ATE503734T1 (de) * | 2004-10-08 | 2011-04-15 | Ibiden Co Ltd | Honigwabenstruktur und verfahren zur herstellung |
KR20080042902A (ko) * | 2004-12-27 | 2008-05-15 | 이비덴 가부시키가이샤 | 세라믹 허니컴 구조체 |
JP4870558B2 (ja) * | 2004-12-27 | 2012-02-08 | イビデン株式会社 | ハニカム構造体及びシール材層 |
JP5237630B2 (ja) * | 2005-02-01 | 2013-07-17 | イビデン株式会社 | ハニカム構造体 |
WO2006103786A1 (ja) * | 2005-03-28 | 2006-10-05 | Ibiden Co., Ltd. | ハニカム構造体およびシール材 |
WO2006137151A1 (ja) * | 2005-06-24 | 2006-12-28 | Ibiden Co., Ltd. | ハニカム構造体、及び、排気ガス浄化装置 |
JP5031562B2 (ja) * | 2005-06-24 | 2012-09-19 | イビデン株式会社 | ハニカム構造体 |
JP5091672B2 (ja) * | 2005-06-24 | 2012-12-05 | イビデン株式会社 | ハニカム構造体及びその製造方法 |
JP5042824B2 (ja) * | 2005-06-24 | 2012-10-03 | イビデン株式会社 | ハニカム構造体、ハニカム構造体集合体及びハニカム触媒 |
CN100537482C (zh) * | 2005-06-24 | 2009-09-09 | 揖斐电株式会社 | 蜂窝结构体 |
WO2006137150A1 (ja) | 2005-06-24 | 2006-12-28 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2006137163A1 (ja) | 2005-06-24 | 2006-12-28 | Ibiden Co., Ltd. | ハニカム構造体 |
JPWO2006137158A1 (ja) * | 2005-06-24 | 2009-01-08 | イビデン株式会社 | ハニカム構造体 |
CN100534617C (zh) * | 2005-06-24 | 2009-09-02 | 揖斐电株式会社 | 蜂窝结构体 |
WO2006137164A1 (ja) * | 2005-06-24 | 2006-12-28 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2006137155A1 (ja) * | 2005-06-24 | 2006-12-28 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2006137149A1 (ja) | 2005-06-24 | 2006-12-28 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2006137157A1 (ja) * | 2005-06-24 | 2006-12-28 | Ibiden Co., Ltd. | ハニカム構造体 |
JP2007275869A (ja) * | 2006-03-17 | 2007-10-25 | Ngk Insulators Ltd | セル構造体の製造方法 |
US20080118701A1 (en) * | 2006-11-16 | 2008-05-22 | Ibiden Co., Ltd. | Method for manufacturing honeycomb structure, and honeycomb structure |
WO2008059607A1 (fr) * | 2006-11-16 | 2008-05-22 | Ibiden Co., Ltd. | Procédé permettant de produire une structure en nid d'abeilles et structure en nid d'abeilles ainsi formée |
JPWO2008059576A1 (ja) * | 2006-11-16 | 2010-02-25 | イビデン株式会社 | ハニカム構造体及びその製造方法 |
EP1923373B1 (en) * | 2006-11-16 | 2010-01-20 | Ibiden Co., Ltd. | Method for manufacturing honeycomb structured body |
US20080179782A1 (en) * | 2007-01-31 | 2008-07-31 | Geo2 Technologies, Inc. | Extruded Fibrous Silicon Carbide Substrate and Methods for Producing the Same |
WO2008096413A1 (ja) * | 2007-02-06 | 2008-08-14 | Ibiden Co., Ltd. | ハニカム構造体 |
WO2008129670A1 (ja) * | 2007-04-17 | 2008-10-30 | Ibiden Co., Ltd. | 触媒担持ハニカムおよびその製造方法 |
US7910514B2 (en) * | 2007-08-09 | 2011-03-22 | Nissan Motor Co., Ltd. | Inorganic fiber catalyst, production method thereof and catalyst structure |
WO2009050775A1 (ja) * | 2007-10-15 | 2009-04-23 | Ibiden Co., Ltd. | ハニカム構造体の製造方法 |
WO2009118815A1 (ja) * | 2008-03-24 | 2009-10-01 | イビデン株式会社 | ハニカム構造体 |
KR101117467B1 (ko) * | 2008-05-20 | 2012-03-07 | 이비덴 가부시키가이샤 | 허니컴 구조체 |
WO2009141893A1 (ja) * | 2008-05-20 | 2009-11-26 | イビデン株式会社 | ハニカム構造体 |
CA2745034C (en) | 2008-12-15 | 2014-01-21 | Unifrax I Llc | Ceramic honeycomb structure skin coating |
DE102009015420A1 (de) * | 2009-03-27 | 2010-09-30 | Emitec Gesellschaft Für Emissionstechnologie Mbh | Wabenkörper für ein Abgasreinigungssystem |
US8539760B2 (en) * | 2010-09-14 | 2013-09-24 | GM Global Technology Operations LLC | Catalyst materials for NOx oxidation in an exhaust aftertreatment system that uses passive ammonia SCR |
CN114832809B (zh) * | 2022-05-23 | 2023-08-01 | 江苏龙净科杰环保技术有限公司 | 一种中低温蜂窝多孔状脱硝催化剂、制备方法及其应用 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003081001A1 (fr) * | 2002-03-22 | 2003-10-02 | Ibiden Co., Ltd. | Filtre en nid d'abeille pour clarification de gaz d'echappement |
WO2003084640A1 (fr) * | 2002-04-09 | 2003-10-16 | Ibiden Co., Ltd. | Filtre en nid d'abeille pour la clarification d'un gaz d'echappement |
WO2004031101A1 (ja) * | 2002-10-07 | 2004-04-15 | Ibiden Co., Ltd. | ハニカム構造体 |
JP2005218935A (ja) * | 2004-02-04 | 2005-08-18 | Ibiden Co Ltd | ハニカム構造体、ハニカム構造体集合体及びハニカム触媒 |
JP2005349378A (ja) * | 2003-12-26 | 2005-12-22 | Ibiden Co Ltd | ハニカム構造体 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3389851B2 (ja) | 1997-01-21 | 2003-03-24 | トヨタ自動車株式会社 | 排ガス浄化用触媒 |
DE60032391T2 (de) * | 1999-09-29 | 2007-10-11 | Ibiden Co., Ltd., Ogaki | Wabenfömiger Filter und Anordnung von keramischen Filtern |
JP4136319B2 (ja) * | 2000-04-14 | 2008-08-20 | 日本碍子株式会社 | ハニカム構造体及びその製造方法 |
KR100632161B1 (ko) * | 2003-02-28 | 2006-10-11 | 이비덴 가부시키가이샤 | 세라믹 하니컴 구조체 |
JP2007098274A (ja) * | 2005-10-04 | 2007-04-19 | Ibiden Co Ltd | 多孔質ハニカム構造体及びそれを利用した排ガス浄化装置 |
WO2008059607A1 (fr) | 2006-11-16 | 2008-05-22 | Ibiden Co., Ltd. | Procédé permettant de produire une structure en nid d'abeilles et structure en nid d'abeilles ainsi formée |
EP1923373B1 (en) | 2006-11-16 | 2010-01-20 | Ibiden Co., Ltd. | Method for manufacturing honeycomb structured body |
US20080118701A1 (en) | 2006-11-16 | 2008-05-22 | Ibiden Co., Ltd. | Method for manufacturing honeycomb structure, and honeycomb structure |
WO2008096413A1 (ja) | 2007-02-06 | 2008-08-14 | Ibiden Co., Ltd. | ハニカム構造体 |
JPWO2008126305A1 (ja) | 2007-03-30 | 2010-07-22 | イビデン株式会社 | 触媒担持体および排気ガス処理装置 |
WO2008126306A1 (ja) | 2007-03-30 | 2008-10-23 | Ibiden Co., Ltd. | 触媒担持体 |
JPWO2008126307A1 (ja) | 2007-03-30 | 2010-07-22 | イビデン株式会社 | 触媒担持体および触媒担持体の製造方法 |
WO2008129670A1 (ja) | 2007-04-17 | 2008-10-30 | Ibiden Co., Ltd. | 触媒担持ハニカムおよびその製造方法 |
-
2006
- 2006-04-14 JP JP2007523349A patent/JP5042827B2/ja not_active Expired - Fee Related
- 2006-04-14 CN CN200680015512A patent/CN100574882C/zh not_active Expired - Fee Related
- 2006-04-14 KR KR1020077025381A patent/KR100891892B1/ko not_active IP Right Cessation
- 2006-04-14 WO PCT/JP2006/307955 patent/WO2007000847A1/ja active Application Filing
- 2006-06-27 EP EP06013270.1A patent/EP1752203B1/en not_active Not-in-force
- 2006-06-28 US US11/475,967 patent/US7794815B2/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003081001A1 (fr) * | 2002-03-22 | 2003-10-02 | Ibiden Co., Ltd. | Filtre en nid d'abeille pour clarification de gaz d'echappement |
WO2003084640A1 (fr) * | 2002-04-09 | 2003-10-16 | Ibiden Co., Ltd. | Filtre en nid d'abeille pour la clarification d'un gaz d'echappement |
WO2004031101A1 (ja) * | 2002-10-07 | 2004-04-15 | Ibiden Co., Ltd. | ハニカム構造体 |
JP2005349378A (ja) * | 2003-12-26 | 2005-12-22 | Ibiden Co Ltd | ハニカム構造体 |
JP2005218935A (ja) * | 2004-02-04 | 2005-08-18 | Ibiden Co Ltd | ハニカム構造体、ハニカム構造体集合体及びハニカム触媒 |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008126328A1 (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 |
JPWO2008126328A1 (ja) * | 2007-03-30 | 2010-07-22 | イビデン株式会社 | ハニカムフィルタ |
US7947231B2 (en) | 2007-03-30 | 2011-05-24 | Ibiden Co., Ltd. | Honeycomb structure, method for manufacturing honeycomb structure, and exhaust gas purifying apparatus |
JP2016187806A (ja) * | 2011-02-28 | 2016-11-04 | コーニング インコーポレイテッド | 二酸化炭素を捕捉するための物品 |
CN106536883A (zh) * | 2014-07-25 | 2017-03-22 | 曼柴油机和涡轮机欧洲股份公司 | 催化器装置和废气催化器 |
JP2017521596A (ja) * | 2014-07-25 | 2017-08-03 | マン・ディーゼル・アンド・ターボ・エスイー | 触媒ユニットおよび排気ガス触媒コンバータ |
US10077701B2 (en) | 2014-07-25 | 2018-09-18 | Man Energy Solutions Se | Catalyst unit and exhaust gas catalyst |
JP2016061532A (ja) * | 2014-09-19 | 2016-04-25 | 日本碍子株式会社 | 熱・音波変換部品および熱・音波変換ユニット |
US11648543B2 (en) | 2017-05-31 | 2023-05-16 | National University Corporation Hokkaido University | Functional structural body and method for making functional structural body |
JPWO2018221692A1 (ja) * | 2017-05-31 | 2020-05-28 | 国立大学法人北海道大学 | 機能性構造体及び機能性構造体の製造方法 |
US11648538B2 (en) | 2017-05-31 | 2023-05-16 | National University Corporation Hokkaido University | Functional structural body and method for making functional structural body |
US11648542B2 (en) | 2017-05-31 | 2023-05-16 | National University Corporation Hokkaido University | Functional structural body and method for making functional structural body |
US11655157B2 (en) | 2017-05-31 | 2023-05-23 | National University Corporation Hokkaido University | Functional structural body and method for making functional structural body |
US11654422B2 (en) | 2017-05-31 | 2023-05-23 | Furukawa Electric Co., Ltd. | Structured catalyst for catalytic cracking or hydrodesulfurization, catalytic cracking apparatus and hydrodesulfurization apparatus including the structured catalyst, and method for producing structured catalyst for catalytic cracking or hydrodesulfurization |
US11666894B2 (en) | 2017-05-31 | 2023-06-06 | Furukawa Electric Co., Ltd. | Structured catalyst for CO shift or reverse shift and method for producing same, CO shift or reverse shift reactor, method for producing carbon dioxide and hydrogen, and method for producing carbon monoxide and water |
US11680211B2 (en) | 2017-05-31 | 2023-06-20 | Furukawa Electric Co., Ltd. | Structured catalyst for hydrodesulfurization, hydrodesulfurization device including the structured catalyst, and method for producing structured catalyst for hydrodesulfurization |
US11684909B2 (en) | 2017-05-31 | 2023-06-27 | Furukawa Electric Co., Ltd. | Structured catalyst for methanol reforming, methanol reforming device, method for producing structured catalyst for methanol reforming, and method for producing at least one of olefin or aromatic hydrocarbon |
JP7352909B2 (ja) | 2017-05-31 | 2023-09-29 | 国立大学法人北海道大学 | 機能性構造体及び機能性構造体の製造方法 |
US11904306B2 (en) | 2017-05-31 | 2024-02-20 | Furukawa Electric Co., Ltd. | Catalyst structure and method for producing the catalyst structure |
US12030041B2 (en) | 2017-05-31 | 2024-07-09 | Furukawa Electric Co., Ltd. | Structured catalyst for steam reforming, reforming apparatus provided with structured catalyst for steam reforming, and method for manufacturing structured catalyst for steam reforming |
US12115523B2 (en) | 2017-05-31 | 2024-10-15 | National University Corporation Hokkaido University | Functional structural body and method for making functional structural body |
Also Published As
Publication number | Publication date |
---|---|
US7794815B2 (en) | 2010-09-14 |
KR100891892B1 (ko) | 2009-04-03 |
CN101171083A (zh) | 2008-04-30 |
JPWO2007000847A1 (ja) | 2009-01-22 |
CN100574882C (zh) | 2009-12-30 |
EP1752203A1 (en) | 2007-02-14 |
EP1752203B1 (en) | 2014-06-25 |
US20070004593A1 (en) | 2007-01-04 |
JP5042827B2 (ja) | 2012-10-03 |
KR20080002918A (ko) | 2008-01-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2007000847A1 (ja) | ハニカム構造体 | |
JP4975619B2 (ja) | ハニカム構造体 | |
JP5031562B2 (ja) | ハニカム構造体 | |
JP5042632B2 (ja) | ハニカム構造体 | |
JP5191657B2 (ja) | セラミックハニカム構造体 | |
JP4815108B2 (ja) | ハニカム構造体 | |
JP5042824B2 (ja) | ハニカム構造体、ハニカム構造体集合体及びハニカム触媒 | |
JP5161458B2 (ja) | ハニカム構造体の製造方法 | |
JP4864061B2 (ja) | ハニカム構造体及びその製造方法 | |
JPWO2006025283A1 (ja) | 排気浄化システム | |
JPWO2006137158A1 (ja) | ハニカム構造体 | |
JPWO2008126309A1 (ja) | 混合粒子及びハニカム構造体 | |
CN111107932B (zh) | 蜂窝催化剂 | |
EP3689454A1 (en) | Honeycomb catalyst | |
JP6726148B2 (ja) | 排ガス浄化用ハニカム触媒 | |
WO2009118871A1 (ja) | ハニカム構造体 | |
JP6949019B2 (ja) | ハニカム構造体及び該ハニカム構造体の製造方法 | |
WO2009118873A1 (ja) | ハニカム構造体 | |
JP6771005B2 (ja) | ハニカム構造体の製造方法 | |
JP6845777B2 (ja) | ハニカム触媒の製造方法 | |
JP6782571B2 (ja) | ハニカム構造体 | |
JP6869754B2 (ja) | ハニカム構造体 | |
KR100883946B1 (ko) | 세라믹 허니컴 구조체 | |
JP6944833B2 (ja) | ハニカム構造体の製造方法 | |
JP2012197186A (ja) | ハニカム構造体の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200680015512.9 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2007523349 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020077025381 Country of ref document: KR |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 06731891 Country of ref document: EP Kind code of ref document: A1 |