WO2004005184A1 - Metal oxides prepared by flame spray pyrolysis - Google Patents
Metal oxides prepared by flame spray pyrolysis Download PDFInfo
- Publication number
- WO2004005184A1 WO2004005184A1 PCT/IB2003/002172 IB0302172W WO2004005184A1 WO 2004005184 A1 WO2004005184 A1 WO 2004005184A1 IB 0302172 W IB0302172 W IB 0302172W WO 2004005184 A1 WO2004005184 A1 WO 2004005184A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ceria
- zirconia
- anyone
- metal oxide
- metal
- Prior art date
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- 229910044991 metal oxide Inorganic materials 0.000 title claims abstract description 39
- 150000004706 metal oxides Chemical class 0.000 title claims abstract description 39
- 238000005118 spray pyrolysis Methods 0.000 title description 11
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims abstract description 184
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims abstract description 135
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims abstract description 131
- 238000000034 method Methods 0.000 claims abstract description 61
- 239000002904 solvent Substances 0.000 claims abstract description 37
- 238000004519 manufacturing process Methods 0.000 claims abstract description 28
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910052751 metal Inorganic materials 0.000 claims abstract description 25
- 239000002184 metal Substances 0.000 claims abstract description 25
- 239000001301 oxygen Substances 0.000 claims abstract description 25
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 25
- 238000003860 storage Methods 0.000 claims abstract description 17
- 229910003455 mixed metal oxide Inorganic materials 0.000 claims abstract description 11
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims description 40
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 39
- 239000002243 precursor Substances 0.000 claims description 33
- 239000003054 catalyst Substances 0.000 claims description 27
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 18
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 18
- 150000001735 carboxylic acids Chemical class 0.000 claims description 17
- 239000000843 powder Substances 0.000 claims description 16
- 238000010438 heat treatment Methods 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 150000003839 salts Chemical group 0.000 claims description 12
- 238000002485 combustion reaction Methods 0.000 claims description 9
- 239000000446 fuel Substances 0.000 claims description 9
- 239000007789 gas Substances 0.000 claims description 9
- 229910052684 Cerium Inorganic materials 0.000 claims description 8
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- 239000000654 additive Substances 0.000 claims description 8
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 6
- 239000012702 metal oxide precursor Substances 0.000 claims description 5
- 229910052697 platinum Inorganic materials 0.000 claims description 5
- -1 vanadia Chemical compound 0.000 claims description 5
- YOBOXHGSEJBUPB-MTOQALJVSA-N (z)-4-hydroxypent-3-en-2-one;zirconium Chemical compound [Zr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O YOBOXHGSEJBUPB-MTOQALJVSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
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- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
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- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 claims description 2
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- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- VGBWDOLBWVJTRZ-UHFFFAOYSA-K cerium(3+);triacetate Chemical compound [Ce+3].CC([O-])=O.CC([O-])=O.CC([O-])=O VGBWDOLBWVJTRZ-UHFFFAOYSA-K 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
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- 229910052742 iron Inorganic materials 0.000 claims description 2
- 239000011553 magnetic fluid Substances 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
- 229910001092 metal group alloy Inorganic materials 0.000 claims description 2
- 238000004377 microelectronic Methods 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910000510 noble metal Inorganic materials 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 238000009512 pharmaceutical packaging Methods 0.000 claims description 2
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- 239000002994 raw material Substances 0.000 claims description 2
- 229910052702 rhenium Inorganic materials 0.000 claims description 2
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims description 2
- 229910052703 rhodium Inorganic materials 0.000 claims description 2
- 239000010948 rhodium Substances 0.000 claims description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- 239000002887 superconductor Substances 0.000 claims description 2
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims 4
- 229910052727 yttrium Inorganic materials 0.000 claims 3
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 claims 1
- 210000004379 membrane Anatomy 0.000 claims 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 11
- 238000002156 mixing Methods 0.000 description 18
- 239000000047 product Substances 0.000 description 17
- 238000002360 preparation method Methods 0.000 description 13
- 238000002441 X-ray diffraction Methods 0.000 description 11
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- 230000015572 biosynthetic process Effects 0.000 description 6
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 6
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
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- 238000005259 measurement Methods 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 4
- 230000000875 corresponding effect Effects 0.000 description 4
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 4
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- 230000005540 biological transmission Effects 0.000 description 3
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- AERUOEZHIAYQQL-UHFFFAOYSA-K cerium(3+);triacetate;hydrate Chemical compound O.[Ce+3].CC([O-])=O.CC([O-])=O.CC([O-])=O AERUOEZHIAYQQL-UHFFFAOYSA-K 0.000 description 3
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- 238000001556 precipitation Methods 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
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- 230000003197 catalytic effect Effects 0.000 description 2
- 229910000420 cerium oxide Inorganic materials 0.000 description 2
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- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
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- 229910002076 stabilized zirconia Inorganic materials 0.000 description 2
- KLFRPGNCEJNEKU-FDGPNNRMSA-L (z)-4-oxopent-2-en-2-olate;platinum(2+) Chemical compound [Pt+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O KLFRPGNCEJNEKU-FDGPNNRMSA-L 0.000 description 1
- TWQHGBJNKVFWIU-UHFFFAOYSA-N 8-[4-(4-quinolin-2-ylpiperazin-1-yl)butyl]-8-azaspiro[4.5]decane-7,9-dione Chemical compound C1C(=O)N(CCCCN2CCN(CC2)C=2N=C3C=CC=CC3=CC=2)C(=O)CC21CCCC2 TWQHGBJNKVFWIU-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
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- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 240000001781 Xanthosoma sagittifolium Species 0.000 description 1
- WZECUPJJEIXUKY-UHFFFAOYSA-N [O-2].[O-2].[O-2].[U+6] Chemical compound [O-2].[O-2].[O-2].[U+6] WZECUPJJEIXUKY-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
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- 229910002086 ceria-stabilized zirconia Inorganic materials 0.000 description 1
- RCFVMJKOEJFGTM-UHFFFAOYSA-N cerium zirconium Chemical compound [Zr].[Ce] RCFVMJKOEJFGTM-UHFFFAOYSA-N 0.000 description 1
- DRVWBEJJZZTIGJ-UHFFFAOYSA-N cerium(3+);oxygen(2-) Chemical class [O-2].[O-2].[O-2].[Ce+3].[Ce+3] DRVWBEJJZZTIGJ-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 239000000945 filler Substances 0.000 description 1
- 238000010285 flame spraying Methods 0.000 description 1
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
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- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical class [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 description 1
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- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/1409—Abrasive particles per se
-
- 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
- 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
- B01D53/92—Chemical or biological purification of waste gases of engine exhaust gases
- B01D53/94—Chemical or biological purification of waste gases of engine exhaust gases by 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
- B01J23/10—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of rare earths
-
- 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
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/63—Platinum group metals with rare earths or actinides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
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Definitions
- the present invention concerns a specific flame method and metal oxides with specific features that are obtainable by said method, in particular cerium and zirconium oxides with excellent thermal stability and high oxygen exchange capacities.
- Metal oxides in particular mixed metal ox- ides have a broad range of applications such as e.g. ceramics, polymer additives, fillers, pigments, reactive surfaces, catalysts, storage materials, polishing additives, membranes, fuel cells etc.
- metal oxides cerium oxides and in particular ce- rium-zirconium mixed oxides, below referred to as ceria/zirconia.
- Ceria/zirconia are used in the current new generation of Three Way Catalysts (TWC) as key- component due to their high dynamic oxygen exchange capacity [Trovarelli et al . (1996), Kaspar et al . (1999)], however also as Oxidation Catalysts, Ceramics, Polishing agents and Fuel cells, amongst others.
- the ceria switches between its two major oxidation states Ce(III) and Ce(IV) thereby taking up or releasing electrons for the conversion of CO and residuals from the combustion process. Depending on the oxygen partial pressure, it absorbs or releases oxygen and sta- bilizes the air-to-fuel ratio making CO oxidation a fast and reliable process [Taylor (1984)]. It is well established, that the addition of zirconia to ceria as a solid solution greatly enhances the reducibility of the Ce(IV) [Kundakovic (1998); Balducci (1995)]. Different production methods, however, lead to a varying state of molecular mixing of ceria and zirconia.
- EP 1 142 830 focuses on chlorine free powders produced by flame spray pyrolysis and uses precursor solutions of type MeR where R is an organic rest such as methyl, ethyl, or a corresponding alkoxy group or a nitrate an- ion.
- R is an organic rest such as methyl, ethyl, or a corresponding alkoxy group or a nitrate an- ion.
- solvents water or alcohols are used.
- Another object of the present invention is a catalyst comprising ceria and preferably ceria/zirconia and having a monolithic structure.
- Still other objects of the present invention are the use of a metal oxide of the present invention as at least part of a catalytically active system, in particular for combustion engines, or for mechanochemical polishing.
- the method for the production of a metal oxide of the present invention is characterized in that at least one metal oxide precursor is dissolved in a high enthalpy solvent comprising at least one carboxylic acid with a mean carbon content of > 2 carbon atoms in an amount of at least 60 % of total solvent to form a solution, and wherein said solution is then formed into droplets and flame oxidized.
- a precursor or precursor mix, respectively, for FSP needs to carry sufficient metal (s) into the flame, distribute said metal (s) within the flame and support a stable combustion and spray process .
- metals such as for example cerium
- organometallic compounds are known, all organometallic compounds are rather expensive and/or contain other, often undesired elements such as halogenes.
- the process of the present invention involves a cheap, readily available precursor mix which offers the possibility to use FSP to produce mixed metal oxides such as ceria/zirconia based mixed oxides with great homogene- ity on atomic level.
- the precursor mix of the present invention is characterized by enabling a high concentration of dissolved metal precursors and a high combustion enthalpy. By using such precursor mix in FSP, high specific surface area metal oxides, such as ceria based materials, with excellent temperature and phase stability can be produced.
- Figure 1A is a transmission electron micro- scope (TEM) picture of ceria/zirconia Ceo.7Zro.3O2 as prepared.
- Figure IB is a transmission electron microscope (TEM) picture of ceria/zirconia Ceo.7Zro.3O2 after thermal treatment at 900°C showing that such thermal treatment leads to larger particles of similar shape.
- XRD X-ray diffraction spectrum
- Figure 4 is a plot of the lattice parameter a, assuming a cubic system, for Ce x Zr ( i- ⁇ ) O2 as a function of increasing ceria content, wherein the line represents an empirical correlation found by Kim (1989) , valid for doped ceria over a broad range of compositions .
- Figure 5A is a comparison of the specific surface area of flame-spray made ceria, ceria/zirconia, wet-phase made mixed oxides, and a commercial sample.
- Figure 5B gives the average crystal size as determined by XRD for all samples from pure ceria to pure zirconia. Both addition of 10 % ceria to zirconia or 10% zirconia to ceria leads to a pronounced decrease in average crystal size, therefore showing a high degree of stabilisation.
- Figure 6 gives the principle of oxygen stor- age capacity measurements (OSC) .
- Figure 7A compares OSC for reduction of the catalyst by H2 and CO from pure zirconia to pure ceria.
- Figure 8 gives the Pt dispersion as deter- mined by CO-pulse chemisorption of Pt on flame made ceria/zirconia.
- Figure 9 shows the reversibly occurring mass uptake and loss of oxygen of Pt/ceria/zirconia prepared by wet method or FSP, measured at a heating rate of 3°C/min, with both samples taken up to 1100 °C and subjected to repeated pulses of CO or H2 with following pulses of O2 for reoxidation.
- the metal oxides of the present invention are obtainable by a method wherein at least one metal oxide precursor is dissolved in a high enthalpy solvent comprising at least one carboxylic acid to form a solution, and wherein said solution is then formed into droplets and flame oxidized.
- the solvent used in the method of the present invention has a carboxylic acid content by weight of at least 60 %, preferably at least 65 %, more preferably at least 75 %, especially at least 90 %, and most preferably more than 90 %.
- the solvent essentially consists of carboxylic acids (presence of usual impurities of technical solvents is acceptable) , in particular of one carboxylic acid or a mixture of carboxylic acids such that the solvent has a net heat of combustion of at least 15 kJ/g, preferably at least 20 kJ/g, more preferably at least 23 kJ/g.
- carboxylic acids presence of usual impurities of technical solvents is acceptable
- the solvent has a net heat of combustion of at least 15 kJ/g, preferably at least 20 kJ/g, more preferably at least 23 kJ/g.
- an acid mixture having a mean number of carbon atoms per carboxylic group (including the C of said group) of > 2 C atoms, usually at least 2.2 C atoms, preferably at least 3 C atoms, more preferably about 4 to 10 C atoms, most preferably 4 to 8 C atoms.
- 7 C atoms would e.g. correspond to heptanoic acid or a mixture of identical moles of acetic acid (2 C atoms) and dodecanoic acid (12 C atoms) . As long as the above provisions are met, it is not very critical which acids are used.
- Preferred solvent mixes comprise carboxylic acids selected from C3 to C18 monocarboxylic acids, more preferred from C5 to C16 carboxylic acids, and most preferred from C7 to C14 carboxylic acids, or mixtures of two or more of such acids, in combination with formic acid and in particular acetic acid.
- carboxylic acids selected from C3 to C18 monocarboxylic acids, more preferred from C5 to C16 carboxylic acids, and most preferred from C7 to C14 carboxylic acids, or mixtures of two or more of such acids, in combination with formic acid and in particular acetic acid.
- ceria/zirconia mixed metal oxides a mixture of lauric acid and acetic acid, especially in a ratio of 1:1 proved to lead to a product with extraordinary properties .
- acids than unsubstituted mono- carboxylic acids can be used provided that they result in a suitable high enthalpy solvent, e.g. acids with polar substituents such as -OH, - H2 or -CONH2 groups can be used to adjust the solvent to specific needs.
- acids with polar substituents such as -OH, - H2 or -CONH2 groups
- the acids may be saturated or unsaturated.
- a carboxylic acid mixture has the further advantage that by using long chain acids together with short chain acids, the solubility and therewith the obtainable concentration range can be regulated/optimized.
- a solvent in particular a solvent mixture, that is stable at room temperature (no phase separation, no measurable evaporation) may also add to an enhanced storage stability of a precursor mix produced in such a solvent system.
- another solvent is used that is not a carboxylic acid, such solvent usually is a high enthalpy solvent that preferably has a chain length such that it is compatible with at least one long chain carboxylic acid of the solvent system.
- Suitable precursor compounds for the use in the method of the present invention are compounds that are soluble in a solvent as outlined above.
- organic groups comprising salts are preferred, in particular purely organometallic compounds or organometalloid compounds such as a salt of at least one (optionally substi- tuted) carboxylic acid, such as acetic acid, formic acid, but also dicarboxylic acid, oligocarboxylic acid and/or polycarboxylic acid and/or other common organometallic or organometalloid ligands such as acetylacetonate, tet- ramethylacetoacetonate, ethylene diamine and others, op- tionally as hydrate.
- organometallic compounds or organometalloid compounds such as a salt of at least one (optionally substi- tuted) carboxylic acid, such as acetic acid, formic acid, but also dicarboxylic acid, oligocarboxylic acid and/or polycarboxylic acid and
- the salt may also be produced within the solvent mixture in situ, meaning that a suitable salt precursor (namely a metal comprising compound, e.g. an oxide, a carbonate or a pure metal, that reacts with at least one of the components of the solvent to form a so- lution) is brought into the solvent mixture where it then forms the salt or derivative of the solvent (e. g. a carboxylic acid salt of a carboxylic acid from the solvent) .
- the flame has a temperature of at least 1000°C, usually at least 1500°C, preferably at least about 2000°C.
- a preferred range of the flame temperature for many applications is 1600 to 2600°C.
- the average diameter of the droplets can vary depend on the liquid dispersion setup and the properties of the liquid itself. Usually, the average droplet diameter ranges from 0.1 ⁇ to 100 ⁇ m, preferably from 1 ⁇ m to 20 ⁇ m.
- the method is applied in the produc- tion of ceria/zirconia.
- presently preferred precursors are cerium acetate hydrate and zirconium acetylacetonate. With these precursors in a sol- vent consisting of lauric acid and acetic acid in a ratio of 1 : 1, mixed oxides with excellent properties could be obtained, in particular in the range Ce(o.9-o.l) Zr (0.1- 0.9)°2' preferably Ce (0 .8-0.2) Zr (0.2-0.8) °2 •
- the method of the present invention can also be used for the production of other metal oxides, in particular mixed metal oxides.
- Further oxide systems that may be prepared by the inventive method, using specific carboxylic acids as solvent are e.g: Ceria based oxides in general and zirconia based oxides in general, but also LiNb0 3 , BaTi0 3 , SrTi0 3 , CaTi0 3 , Li y Mn0 x and derivatives, NiO, i x TiO y , apatite for medical implants, metal doped titania, rare earth metal oxides, especially lanthanum based perovskites, mixed ox- ides containing an element of the earth metal and from the transition metal group, mixed oxides containing an element from the alkali metals and the transition metals, aluminates, borates, silicates, phosphates, hafnia, tho- ria, uranium oxide, etc.
- Ceria based oxides in general and zirconia based oxides in general but also LiNb0 3 , BaTi0 3
- the method of the present invention may e.g. also be used to produce stabilized zirconia that can e.g. be used for fuel cells.
- Such zirconia preferably contains additional metal oxides such as ceria, yttria and/or alkaline earth metals.
- additional metal oxides such as ceria, yttria and/or alkaline earth metals.
- Most suitable mixed oxides contain less than 20 % ceria or yttria, preferably less than 10%, most preferably less than 8% of the additional oxide.
- the method of the present invention is suitable for the production of any metal oxide where metal oxide precursors, in particular organo etal- lie or organometalloid precursors, in particular purely organometallic or purely organometalloid metal salts have to be dissolved at sufficient concentration in a high enthalpy solvent for high temperature FSP.
- the as-prepared oxides may be subjected directly to an after-treatment in order to form nitrides, carbides, silicides, borides and others .
- inventive method it became possible for the first time to provide metal oxides, in particular mixed metal oxides, that have at least one of the following properties - pure and mixed metal oxides:
- the metal oxides of the present invention have the applications already known for them and an extended field of applica- tions due to their improved properties.
- ceria/zirconia e.g. one of the preferred fields of application is as a catalyst for combustion engine exhaust gases, e.g. in the automotive industry.
- a ceria/zirconia comprising catalyst having a monolithic structure is used.
- Such monolithic structure can e.g.
- the life-time of the differently prepared catalysts may vary.
- the ceria/zirconia catalysts of the present invention can be used together with further catalytically active substances such as further metal oxides, e.g. ti- tania, vanadia, chro ia, manganese, iron, cobalt, nickel, copper oxides and/or noble metals, e.g. platinum, palladium, rhodium, ruthenium, rhenium, iridium, all of them alone or in admixture with one or more thereof, or alloys thereof.
- further catalytically active substances such as further metal oxides, e.g. ti- tania, vanadia, chro ia, manganese, iron, cobalt, nickel, copper oxides and/or noble metals, e.g. platinum, palladium, rhodium, ruthenium, rhenium, iridium, all of them alone or in admixture with one or more thereof, or alloys thereof.
- further catalytically active substances
- the metal oxides of the present invention such as e.g. ceria, zirconia or ceria/zirconia, due to their great homogeneity can be used for mechanochemical polishing.
- Stabilized zirconia made by the present invention may be used in fuel cells, where the high phase homogeneity and the mixing at atomic level favour oxygen ion transport as it has been shown by the OSC measurements. Furthermore, the excellent degree of mixing obtained by the method of the present invention allows for high thermal and mechanical stability, as crystallites stay very small (see Figure 5B) , thus reducing the chance of crack formation. This properties make the ceria- stabilized zirconia of the present invention highly suitable for high-temperature and low-temperature fuel cell application. Given the homogeneous particle structure, the oxides of the present invention are furthermore suitable for the manufacture of coatings, in structural ceramics or for protecting layers on metals . Applications for other metal oxides are e.g.
- heterogenous catalysts as structural ceramics, as battery storage materials, for chemical sensors, for elements in energy production, for solar energy production elements, for electron storage in recyclable battery units, as dielectrics, as gas permeable membranes, as pigments, polymer additives, stabilizers, magnetic fluids, polishing powders, additives in metal alloys, in armor fabrication, in microelectronics, as electrode raw material, as phosphors for radiation sensitive elements and in displays, cosmetics, pharmaceutical packaging, additive in food and pharmaceutical applications, fuel cells, superconductors and others.
- Preparation of Precursor-Mix Corresponding amounts of cerium acetate hydrate and zirconium acetylacetonate were dissolved in the above mixture to a total metal concentration of 0.15 mole/1. These precursor solutions were stable at ambient conditions and could readily be sprayed. Their high en- thalpy content combined with the capability to dissolve readily available, polar metal ions, makes these mixtures suitable for the preparation of mixed oxides.
- Figure 1A depicts a TEM (transmission electron microscope) picture of as-prepared ceria/zirconia Ceo.7 Zr 0 . 3 O 2 .
- the product consists of well-crystalline, sharp edged nanoparticles of 4-10 nm diameter. No large lumps of ceria could be detected. This corroborates sufficient enthalpy delivery and good dispersion of the metal precursor in the flame. If the powders obtained according to the present invention are heated for 2 h at 900°C, a clear difference in specific surface area is visible (see Figure IB) . While the preparation disclosed by Madler et al .
- the broad signals from the stable mixed ceria/zirconia phase slowly shift to higher diffraction angle (two theta) .
- This smooth shift from pure ceria to pure zirconia corroborates the extreme mixing of the as- prepared ceria/zirconia.
- the continuous transition may best be observed for the peak around 50°.
- Figure 2 B gives the XRD signals for the same samples, heated to 900° C for two hours in air. Due to thermal treatment, the peaks get narrower. The solid solution is stable, however, even after this high temperature treatment.
- Figure 3 gives the specific surface area of as-prepared Ce x Zr ( i- ⁇ ) 02 (squares) and calcined powders (circles) . While the specific surface area of zirconia containing powders is generally constant, a drop is found for pure ceria. The mere addition of 10 atom-% zirconium to ceria already leads to considerable stabilisation. Further increasing the zirconia content has only a minor effect on the specific surface area. Interestingly, after thermal treatment at 900°C for 2 h in air, all powders have similar specific surface area, further compared in Figure 5A.
- Figure 4 plots the lattice parameter a, assuming a cubic system, for Ce x Zr(i- ⁇ )0 2 as a function of increasing ceria content.
- the smaller zirconia kation Zr + substitutes Ce 4+ ions in the ceria lattice and squeezes the crystal, leading to a smaller unit cell with reduced a.
- the line in Fig. 4 represents an empirical correlation found by Kim (1989) , valid for doped ceria over a broad range of compositions.
- the as-prepared powders follow the correlation with minor deviations. Thermal treatment of the product did not affect the mixed oxide phases and the formation of separate phases could not be detected by XRD in any sample.
- Figure 5A compares the specific surface area of flame-spray made ceria, ceria/zirconia and wet-phase made mixed oxides and commercial Rhodia ceria/zirconia.
- Trovarelli et al. (1997) prepared ceria by high energy ball mixing but obtain poor mixing at an atomic level.
- Terribile et al . (1998) prepared ceria by a hybrid organic/inorganic route and found excellent specific surface areas. Calcination, however, reduced the surface area to about 43 m ⁇ /g.
- Figure 5A further compares materials of this invention to commercially available ceria/zirconia supplied by Rhodia. The commercial catalyst stays around 50 m ⁇ /g while the material of this invention exceeds well beyond that.
- Figure 5B shows the minimum crystal size for intermediate composition that proofs the extreme degree of mixing.
- FIG. 6 gives the principle of oxygen storage capacity (OSC) measurments as described by Rocchini et al. (2000) and Trovarelli et al . (1997).
- the sample 50 mg is placed in a thermographimetric balance and subjected to pulses (2 ml) of hydrogen and oxygen. The loss of mass is due to removed oxygen. The material is fully reoxidized by the second puls, corroborating the dynamic oxygen storage capacity.
- OSC is measured for both hydrogen and CO, both leading to the same degree of re- duction.
- OSC oxygen storage capacity
- Trovarelli et al. (1997) report maximum dynamic OSC at x around 0.8.
- the flame made samples in this work show a maximum OSC related to mass at intermediate zirconia content (x around 0.5), therefore they require less of ceria for the same dynamic OSC per mass.
- Ceria/zirconia mixed oxides of high specific surface area and good thermal stability can be prepared by flame spray pyrolysis.
- the major process parameters, precursor solution composition, enthalpy delivery and metal concentration in the flame, allow to control the production process over a broad range of conditions.
- molecular mixing e.g. in the synthesis of ceria/zirconia, is of great importance. Such molecular mixing is dependent on the phase stability. Due to insufficient mixing or partial precipitation in the precursor mix, significant affection of properties of the mixed metal oxides prepared from such inhomogeneous precursor mixes has been found.
- the product ceria/zirconia may be characterized as an intimately mixed solid solution and forms a stable phase up to high zirconia contents.
- mixed oxides with increased thermal stability of flame-made mixed oxides could be provided. This may be associated with the high preparation temperature favoring a pre-equilibrated structure and uniform mor- phology, both enhancing the thermal stability.
- Increased molecular mixing in ceria/zirconia results in much higher ceria usage, both facilitating the catalytic process and lowering production costs, since cheaper zirconium precursors can be used in larger quantities, e.g. up to Ceo .2 Zr 0.8°2' that has been found to still have e.g. as good OSC as Ceo.sZro.2O2-
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Also Published As
Publication number | Publication date |
---|---|
JP2005537204A (en) | 2005-12-08 |
JP4416651B2 (en) | 2010-02-17 |
CN1665743A (en) | 2005-09-07 |
US7211236B2 (en) | 2007-05-01 |
AU2003228051A1 (en) | 2004-01-23 |
EP1517853A1 (en) | 2005-03-30 |
CN100475688C (en) | 2009-04-08 |
BR0312339A (en) | 2005-04-12 |
EP1517853B1 (en) | 2012-06-27 |
US20040126298A1 (en) | 2004-07-01 |
CA2488920A1 (en) | 2004-01-15 |
EP1378489A1 (en) | 2004-01-07 |
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