US2004219087A1PendingUtilityA1
Metal oxide powder and method for the production of the same
Est. expiryAug 11, 2013(expired)· nominal 20-yr term from priority
Inventors:Masahide MohriHironobu KoikeShinichiro TanakaTetsu UmedaHisashi WatanabeKunio SaegusaAkira Hasegawa
C01F 17/34C01F 5/06C09K 3/1436C01P 2004/61C01P 2006/12C01G 23/047C01P 2002/02C01P 2004/62C01B 13/185C01P 2004/30C01P 2004/52C01F 5/02C01P 2002/72C01P 2002/30C01B 13/32C01G 15/00C01G 49/06C01G 19/02C01P 2004/50C01G 25/02C01P 2002/50C01P 2004/03C01P 2004/51C01B 13/18C01P 2004/54C01B 13/14C01G 49/0054C01F 17/235
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Claims
Abstract
A metal oxide powder except α-alumina, comprising polyhedral particles having at least 6 planes each, a number average particle size of from 0.1 to 300 μm, and a D 90 /D 10 ratio of 10 or less where D 10 and D 90 are particle sizes at 10% and 90% accumulation, respectively from the smallest particle size side in a cumulative particle size curve of the particles. This metal oxide powder contains less agglomerated particles, and has a narrow particle size distribution and a uniform particle shape.
Claims
exact text as granted — not AI-modified1 . A metal oxide powder except α-alumina, comprising polyhedral particles having at least 6 planes each, a number average particle size of 0.1 to 40 μm and a D 90 /D 10 ratio of 5 or less where D 10 and D 90 are particle sizes at 10% and 90% accumulation, respectively from the smallest particle size side in a cumulative particle size curve of the particles, and
wherein a ratio of agglomerated particle size to a primary particle size is from 1 to 6, and the metal oxide is a metal oxide of a metal element selected from the group consisting of the metal elements of the Group Ib, II, III, V, VI, VII and VIII of the Periodic Table.
2 - 3 . (canceled).
4 . The metal oxide powder according to claim 1 , wherein said ratio of a primary particle size to an agglomerated particle size is from 1 to 3.
5 . (canceled).
6 . The metal oxide powder according to any one of claims 1 and 4 , wherein said metal oxide is a simple metal oxide titanium.
7 . The metal oxide powder according to any one of claims 1 and 4 , wherein said metal oxide is a simple metal oxide of a metal selected from the group consisting of magnesium, zirconium and iron.
8 . The metal oxide powder according to any one of claims 1 and 4 , wherein said metal oxide is a simple metal oxide of cerium.
9 . The metal oxide powder according to any one of claims 1 and 4 , wherein said metal oxide is a simple metal oxide of a metal selected from the group consisting of indium and tin.
10 . The metal oxide powder according to any one of claims 1 and 4 , wherein said metal oxide is a simple metal oxide of a metal selected from the group consisting of zinc, cadmium, gallium, germanium, niobium, tantalum, antimony, bismuth, chromium, molybdenum, manganese, cobalt, nickel and uranium.
11 . A rutile type titanium oxide powder comprising polyhedral particles each having at least 8 planes, a number average particle size of from 0.1 to 300 μm, a D 90 /D 10 ratio of 5 or less where D 10 and D 90 are particle sizes at 10% and 90% accumulation, respectively from the smallest particle size side in a cumulative particle size curve of the particles, and a ratio of agglomerated particle size to primary particle size of the particles is from 1 to 6.
12 . The rutile type titanium oxide powder according to claim 11 , wherein a ratio of an agglomerated particle size to a primary particle size is from 1 to 2, and a BET specific surface area is from 0.1 to 10 m 2 /g.
13 . A method for producing a calcined metal oxide powder having a narrow particle size distribution except α-alumina, comprising calcining a metal oxide powder or a metal oxide precursor powder in the presence or absence of a seed crystal in an atmosphere containing at least one gas selected from the group consisting of (1) a hydrogen halide, (2) a component prepared from a molecular halogen and steam and (3) a molecular halogen.
14 . The method according to claim 13 , wherein said calcination is carried out in the presence of a seed crystal.
15 . The method according to claim 13 or 14 , wherein said gas contained in said atmosphere gas is a hydrogen halide.
16 . The method according to claim 15 , wherein said hydrogen halide is hydrogen chloride or hydrogen bromide.
17 . The method according to claim 15 , wherein said hydrogen halide is hydrogen fluoride.
18 . The method according to claim 15 , wherein a concentration of said hydrogen halide is at least 1 vol. % of said atmospheric gas.
19 . The method according to claim 13 or 14 , wherein said gas contained in said atmosphere gas is said component prepared from a molecular halogen and steam.
20 . The method according to claim 19 , wherein said molecular halogen is chlorine or bromine.
21 . The method according to claim 19 , wherein said molecular halogen is fluorine.
22 . The method according to claim 19 , wherein said component is prepared from at least 1 vol. % of said molecular halogen and at least 0.1 vol. % of steam, both based on said atmosphere gas.
23 . The method according to claim 13 or 14 , wherein said gas contained in said atmosphere gas is a molecular halogen which is chlorine or bromine, and a concentration of said molecular halogen in said atmosphere gas is at least 1 vol. %.
24 . The method according to claim 13 , wherein said metal oxide powder or metal oxide precursor powder has a bulk density of 40% or less of a theoretical value.
25 . The method according to claim 14 , wherein said seed crystal had a bulk density of 40% or less of a theoretical value.
26 . The method according to claim 13 or 14 , wherein said metal oxide having a narrow particle size distribution except α-alumina is formed on a site where said metal oxide powder or metal oxide precursor powder to be calcined is present.
27 . The method according to claim 13 or 14 , wherein said metal oxide powder or metal oxide precursor powder to be calcined is a metal oxide powder or metal oxide precursor powder of a metal element selected from the group consisting of the metal elements of the Groups Ib, II, III, IV, V, VI, VII and VIII of the Periodic Table.
28 The method according to claim 13 or 14 , wherein said metal oxide powder or metal oxide precursor powder is a metal oxide powder or metal oxide precursor powder of a metal selected from the group consisting of magnesium, titanium, and iron.
29 - 30 . (canceled).
31 . The method according to claim 13 or 14 , wherein said metal oxide powder or metal oxide precursor powder is a metal oxide powder or metal oxide precursor powder of a metal selected from the group consisting of zinc, cadmium, gallium, germanium, niobium, tantalum, antimony, bismuth, chromium, molybdenum, manganese, cobalt, nickel and uranium.
32 . A method for producing a calcined metal oxide powder having a narrow particle size distribution except α-alumina, comprising calcining a metal oxide powder or a metal oxide precursor powder in the presence or absence of a seed crystal in an atmosphere containing at least one gas selected from the group consisting of (1) a hydrogen halide, and (2) a component prepared from a molecular halogen and steam.Join the waitlist — get patent alerts
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