WO2004014800A1 - Doped zinc oxide powder, process for its preparation, and its use - Google Patents
Doped zinc oxide powder, process for its preparation, and its use Download PDFInfo
- Publication number
- WO2004014800A1 WO2004014800A1 PCT/EP2003/007247 EP0307247W WO2004014800A1 WO 2004014800 A1 WO2004014800 A1 WO 2004014800A1 EP 0307247 W EP0307247 W EP 0307247W WO 2004014800 A1 WO2004014800 A1 WO 2004014800A1
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- Prior art keywords
- zinc oxide
- oxide powder
- zone
- zinc
- doping
- Prior art date
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- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 title claims abstract description 55
- 238000000034 method Methods 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 46
- 239000002019 doping agent Substances 0.000 claims abstract description 38
- 230000003647 oxidation Effects 0.000 claims abstract description 25
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 25
- 230000006911 nucleation Effects 0.000 claims abstract description 24
- 238000010899 nucleation Methods 0.000 claims abstract description 24
- 239000011701 zinc Substances 0.000 claims abstract description 21
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 21
- 238000009834 vaporization Methods 0.000 claims abstract description 20
- 238000010791 quenching Methods 0.000 claims abstract description 15
- 230000000171 quenching effect Effects 0.000 claims abstract description 15
- 239000011164 primary particle Substances 0.000 claims abstract description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 5
- 239000004411 aluminium Substances 0.000 claims abstract description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000000576 coating method Methods 0.000 claims abstract description 5
- 229910052738 indium Inorganic materials 0.000 claims abstract description 5
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052718 tin Inorganic materials 0.000 claims abstract description 5
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 4
- 229910052732 germanium Inorganic materials 0.000 claims abstract description 4
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000004922 lacquer Substances 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 239000000443 aerosol Substances 0.000 claims description 13
- 229910001868 water Inorganic materials 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 239000000567 combustion gas Substances 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- 239000001301 oxygen Substances 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 230000005540 biological transmission Effects 0.000 claims description 8
- 239000011541 reaction mixture Substances 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical group [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 5
- 229910003437 indium oxide Inorganic materials 0.000 claims description 4
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000000112 cooling gas Substances 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- 239000011261 inert gas Substances 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 3
- 229910001887 tin oxide Inorganic materials 0.000 claims description 3
- 150000004703 alkoxides Chemical class 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 238000009472 formulation Methods 0.000 claims description 2
- 150000002823 nitrates Chemical class 0.000 claims description 2
- 230000037072 sun protection Effects 0.000 claims description 2
- 238000009835 boiling Methods 0.000 abstract description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 30
- 239000001257 hydrogen Substances 0.000 description 18
- 229910052739 hydrogen Inorganic materials 0.000 description 18
- 239000000843 powder Substances 0.000 description 16
- 229910052757 nitrogen Inorganic materials 0.000 description 15
- 239000007789 gas Substances 0.000 description 12
- 239000002245 particle Substances 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 10
- 150000002431 hydrogen Chemical class 0.000 description 8
- PSCMQHVBLHHWTO-UHFFFAOYSA-K indium(iii) chloride Chemical compound Cl[In](Cl)Cl PSCMQHVBLHHWTO-UHFFFAOYSA-K 0.000 description 8
- 235000014692 zinc oxide Nutrition 0.000 description 8
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 6
- 238000001914 filtration Methods 0.000 description 5
- 239000011787 zinc oxide Substances 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 238000010191 image analysis Methods 0.000 description 3
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 3
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000003917 TEM image Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- AJNVQOSZGJRYEI-UHFFFAOYSA-N digallium;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Ga+3].[Ga+3] AJNVQOSZGJRYEI-UHFFFAOYSA-N 0.000 description 1
- 229910001195 gallium oxide Inorganic materials 0.000 description 1
- 238000002173 high-resolution transmission electron microscopy Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G9/00—Compounds of zinc
- C01G9/02—Oxides; Hydroxides
- C01G9/03—Processes of production using dry methods, e.g. vapour phase processes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/27—Zinc; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G9/00—Compounds of zinc
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G9/00—Compounds of zinc
- C01G9/02—Oxides; Hydroxides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/04—Compounds of zinc
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/04—Compounds of zinc
- C09C1/043—Zinc oxide
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/50—Solid solutions
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/54—Particles characterised by their aspect ratio, i.e. the ratio of sizes in the longest to the shortest dimension
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/64—Nanometer sized, i.e. from 1-100 nanometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/12—Surface area
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/40—Electric properties
-
- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
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- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
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- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2993—Silicic or refractory material containing [e.g., tungsten oxide, glass, cement, etc.]
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- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2993—Silicic or refractory material containing [e.g., tungsten oxide, glass, cement, etc.]
- Y10T428/2995—Silane, siloxane or silicone coating
-
- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2993—Silicic or refractory material containing [e.g., tungsten oxide, glass, cement, etc.]
- Y10T428/2996—Glass particles or spheres
Definitions
- the invention relates to a doped zinc oxide powder, to its preparation and to its use.
- Electrically conductive materials are required for many applications, such as, for example, in plastics, lacquers, coatings or fibres. In addition to electrical conductivity, it is in many cases desirable for such materials also to be largely transparent, for example in the case of pale or coloured coatings .
- Examples of conductive materials are zinc oxides doped with oxides of the metals of the third or fourth main group.
- EP-A-598284 describes a process for the preparation of doped zinc oxide by oxidation of zinc vapour in the presence of doping agents selected from the group of the chlorides and bromides of aluminium, gallium, indium, tin, germanium or silicon.
- doping agents selected from the group of the chlorides and bromides of aluminium, gallium, indium, tin, germanium or silicon.
- the doping agents are limited so that they must be free of oxygen atoms and their boiling points must not be higher than that of the zinc.
- the known preparation processes usually yield needle-shaped or three-dimensionally branched, needle-shaped particles having sizes in the micrometre range. Such particles can have advantages over spherical particles in terms of electrical conductivity. However, their poor sintering behaviour and their poor dispersibility are disadvantageous .
- Known spherical, doped zinc oxide particles are obtained by calcination of zinc oxide powder and gallium oxide in the presence of carbon in a reducing atmosphere (JP58-145620) .
- the object of the invention is to prepare an electrically conductive doped zinc oxide powder which has high transparency and does not have the disadvantages of the prior art.
- the object is achieved by a pyrogenically prepared, doped zinc oxide powder, wherein the doping component comprises at least one oxide from the group comprising aluminium, gallium, indium, germanium, tin, silicon, which is characterised in that the doped zinc oxide powder is in the form of aggregates having a mean maximum diameter of from 30 to 400 nm and the doping component is present in an amount of from 0.005 to 15 wt.%.
- the doping component comprises at least one oxide from the group comprising aluminium, gallium, indium, germanium, tin, silicon, which is characterised in that the doped zinc oxide powder is in the form of aggregates having a mean maximum diameter of from 30 to 400 nm and the doping component is present in an amount of from 0.005 to 15 wt.%.
- flame oxidation is to be understood as meaning the oxidation of zinc to zinc oxide in the gas phase in a flame produced by the reaction of a combustion gas, preferably hydrogen, and oxygen.
- flame hydrolysis is to be understood as meaning the hydrolysis and subsequent oxidation of the doping agents in the same flame. In that process, highly disperse, non-porous primary particles are first formed, which grow together to form aggregates as the reaction progresses, and those aggregates may join together further to form agglomerates.
- Doping component is to be understood as meaning one or more oxides of the above-mentioned metals, as are present in the powder according to the invention.
- Doping agent is to be understood as meaning a substance which carries an above- mentioned metal as metal component and which is converted into the oxide during the preparation of the powder according to the invention.
- the content of doping component in the zinc oxide powder according to the invention is based on the particular oxide in question.
- the primary particles are to be understood as being, in high-resolution TEM images, the smallest particles which obviously cannot be broken down further.
- Several primary particles can join together at their points of contact to form aggregates. Such aggregates are either difficult to separate again by means of dispersing devices or cannot be separated at all.
- Several aggregates can join together loosely to form agglomerates, it being possible for that process to be reversed again by suitable dispersion.
- the mean maximum aggregate diameter is determined by image analysis following ASTM 3849-89. In that process, the maximum diameter of about 1500 aggregates is determined and the arithmetic mean is calculated therefrom. The maximum mean diameter describes the structure of an aggregate more accurately than the mean diameter.
- the mean maximum aggregate diameter of the zinc oxide powder according to the invention may preferably have a value of from 50 to 300 nm and particularly preferably from 80 to 200 nm. Within those ranges, the electrical conductivity and the transparency have particularly advantageous values .
- the aggregates of the powder according to the invention preferably have a largely anistropic structure, defined by a form factor F (circle) of less than 0.5.
- the parameter F (circle) describes the deviation of an aggregate from an ideal circular form. F ⁇ circle) is equal to 1 for an ideal circular object. The smaller the value, -the further the structure of the object from the ideal circular form.
- the definition of the parameter is in accordance with ASTM 3849-89.
- the mean primary particle diameter of the zinc oxide powder according to the invention may advantageously be from 5 to 30 nm.
- the BET surface area of the zinc oxide powder according to the invention may vary within wide limits, from 5 to 100 m 2 /g. Values of from 30 to 70 m 2 /g are preferred.
- the resistivity of the zinc oxide powder may also vary over a wide range.
- zinc oxide is used in the form of an electrically conductive powder, it should. be not more than 10 6 Ohm x cm. It is preferably from 10 2 to 10 4 Ohm x cm, at a compressed density of 1.0 g/cm 3 .
- the transmission of the zinc oxide powder may have a value of more than 70 %. That may be of importance for applications in which high transparency is required.
- the amount of doping component in the zinc oxide powder according to the invention varies from 0.005 to 15 wt.% zinc oxide powder.
- the doping may preferably be from 0.1 to 6.0 wt.%.
- the range from 0.5 to 3.0 wt.% is particularly preferred.
- a preferred doping component may be aluminium oxide.
- a further preferred doping component may be a mixture of indium oxide and tin oxide.
- the amount of indium oxide is preferably from 90 to 99 wt.%, based on the sum of indium oxide and tin oxide, in each case calculated as oxide.
- the invention also provides a process for the preparation of the doped zinc oxide powder according to the invention, which process is characterised in that the powder is obtained in four successive zones, a vaporisation zone, a nucleation zone, an oxidation zone and a quenching zone, from zinc powder and at least one doping agent, - wherein, in the vaporisation zone, zinc powder is vaporised in a flame of air and/or oxygen and a combustion gas, preferably hydrogen, with the proviso that the reaction parameters are so chosen that oxidation of the zinc does not occur,
- the aerosol may be obtained from aqueous, alcoholic and aqueous-alcoholic solutions or suspensions containing at least one doping agent.
- the aerosols may be produced and introduced into the nucleation zone together or separately. Production of the aerosols may be carried out, for example, by means of a binary nozzle or by ultrasonic atomisation.
- the process according to the invention may also be carried out by supplying the doping agent or agents to the nucleation zone in vaporised form instead of in the form of aerosols.
- the doping agents can be vaporised in the same manner as zinc powder, that is to say in a flame of air and/or oxygen and a combustion gas, preferably hydrogen, with the proviso that the reaction parameters are so chosen that oxidation of the doping agent does not occur.
- the doping agents may be vaporised separately or together with the zinc powder.
- the process according to the invention can be carried out by supplying air and/or oxygen and the combustion gas at one or more locations within the vaporisation zone.
- air and/or oxygen and the combustion gas can be supplied at one or more locations within the oxidation zone.
- Separation of the zinc oxide powder from the gas stream may be carried out by means of filters, cyclone, washer or other suitable separators .
- Fig. la-c show a simplified reaction .scheme.
- Fig. la-c show a simplified reaction .scheme.
- A zinc powder
- a v zinc vapour
- a Nu zinc particles in the nucleation zone
- B doping agent
- B v vaporised doping agent
- B Nu doping agent in the nucleation zone
- B Ae doping agent in aerosol form
- C water
- P doped zinc oxide powder
- a combustion gas
- I A zinc powder vaporisation
- I B doping agent vaporisation
- I A+B vaporisation of zinc powder and doping agent together
- l Ae conversion of doping agent into aerosol
- Fig. la shows a variant in which the zinc powder is vaporised and the doping agent is introduced into the nucleation zone in the form of an aerosol.
- Fig. lb - shows a variant in which zinc powder and the doping agent are vaporised together
- Fig. 1-c shows a variant in which they are vaporised separately and fed to the nucleation zone .
- the temperature in the nucleation zone may also be advantageous for the temperature in the nucleation zone to be from 700°C to 800°C.
- process parameters are, for example, the rate of cooling and the dwell time in the individual stages of the process .
- the rate of cooling in the nucleation zone is preferably from 100 K/s to 10,000 K/s, with values from 2000 K/s to 3000 K/s being particularly preferred.
- the rate of cooling in the quenching zone is preferably from 1000 K/s to
- the dwell time in the vaporisation zone is preferably from 0.1 s to 4 s, with values from 0.5 s to 2 s being particularly preferred.
- the dwell time in the nucleation zone is preferably from 0.05 s to 1.00 s, particularly preferably from 0.1 s to 0.2 s.
- the dwell time in the oxidation zone is preferably from 5 ms to 200 ms, with values from 10 ms to 30 ms being particularly preferred.
- the dwell time in the quenching zone is preferably from 0.05 s to 1.00 s, with values from 0.1 s to 0.2 s being particularly preferred.
- Halides, nitrates, alkyls, alkoxides and/or mixtures thereof may be used as doping agents . Particular preference is given to the use of the halides of aluminium, indium and tin.
- the zinc oxide powder according to the invention can be used in electrically conductive, optionally transparent lacquers and coatings, as a filler or in sun protection formulations .
- the doped zinc oxide powder according to the invention acquires its properties, such as, for example, a defined aggregate size, electrical conductivity, or transparency, owing to the novel preparation process .
- the zinc vapour in the process according to the invention is cooled below the boiling point of the zinc prior to the oxidation.
- nucleation with the formation of zinc crystallites is able to occur.
- the doping agent is added to that nucleation zone.
- the BET surface area is determined in accordance with DIN 66131.
- the TEM images are obtained using a Hitachi TEM device, type H-75000-2. Approximately from 500 to 600 aggregates are evaluated by means of the CCD camera of the TEM device and subsequent image analysis .
- the parameter F (shape) is equal to the quotient of the minimum aggregate diameter to the maximum aggregate diameter.
- the parameters F (shape) and F (circle) describe the deviation of a particle from an ideal circular shape.
- F (shape) and F (circle) are 1 for an ideal circular object. The smaller the value, the more removed the structure of the object from the ideal circular shape.
- the transmission of the powders is determined in a dispersion which contains 1 wt.% powder and 99 wt.% water and is dispersed first by means of a dissolver (2000 rpm, 5 min) and then by means of an ultrasonic finger (amplitude 80 %, 4 min) . 2.0 g of the dispersion are removed and made up to 100 g with water. The transmission and scattered light for that dispersion are determined using a turbidimeter (Hach, 2100AN turbidimeter) . Resistivity
- the resistivity of the powders is measured at room temperature and 40 % relative humidity as a function of the compressed density (0.0 - 1.6 g/cm 3 ) .
- the specimen is placed between two movable electrodes, and the current flow is determined after application of a direct current.
- the density of the powder is then increased stepwise by reducing the distance between the electrodes, and the resistance is measured again. The measurement is carried out following DIN IEC 93.
- the zinc powder is vaporised thereby.
- the reaction mixture of zinc vapour, hydrogen, nitrogen and water is then cooled to a temperature of 850°C by the metering in of 2 m 3 /h of nitrogen, and 300 g/h of a 10 wt.% aqueous aluminium chloride solution (A1C1 3 x 6 H 2 0) are fed in in the form of an aerosol.
- 3 m 3 /h of oxidising air and 20 m 3 /h of quenching gas are then added, whereupon the reaction temperature falls to values of about 530°C.
- the doped zinc oxide powder is separated from the gas stream by
- the zinc powder is vaporised thereby.
- the reaction mixture of zinc vapour, hydrogen, nitrogen and water is then cooled to a temperature of 870°C by the metering in of 2 m 3 /h of nitrogen, and 350 g/h of a 5 wt.% aqueous indium(III) chloride solution (InCl 3 x 4 H 2 0) are fed in in the form of an aerosol.
- 3 m 3 /h of oxidising air and 20 m 3 /h of quenching gas are then added, whereupon the reaction temperature falls to values of about • 680°C.
- the doped zinc oxide powder is separated from the
- the zinc powder is vaporised thereby.
- the reaction mixture of zinc vapour, hydrogen, nitrogen and water is then cooled to a temperature of 880°C by the metering in of 2.5 m 3 /h of nitrogen, and 320 g/h of a -6 wt.% aqueous solution of a 95:5 mixture (based on the respective oxides) of indium(III) chloride (InCl 3 x 4 H 2 0) and tin tetrachloride (SnCl 4 ) are fed in in the form of an aerosol. 3 m 3 /h of oxidising air and 20 m 3 /h of quenching gas are then added, whereupon the reaction temperature falls to values of about 650°C.
- the doped zinc oxide powder is separated from the gas stream by filtration.
- the reaction mixture of zinc vapour, doping agent, hydrogen, nitrogen and water is then cooled to a temperature of 990°C by the metering in of 1.5 m 3 /h of nitrogen.
- 5 m 3 /h of oxidising air and 15 m 3 /h of quenching gas are then added, whereupon the reaction temperature falls to values of about 440°C.
- the doped zinc oxide powder is separated from the gas stream by filtration.
- the zinc powder is vaporised thereby.
- the reaction mixture of zinc vapour, hydrogen, nitrogen and water is then cooled to a temperature of 870°C by the metering in of 1.5 m 3 /h of nitrogen. 4 m 3 /h of oxidising air and 30 m 3 /h of quenching gas are then added, whereupon the reaction temperature falls to values of about 300°C.
- the doped zinc oxide powder is separated from the gas stream by filtration.
- the process parameters for the tests are shown in Table 1, and the product properties of the resulting powders are shown in Table 2.
- the powders of Examples 1 and 3 prepared by the process according to the invention have a mean maximum aggregate diameter of approximately from 110 to 150 nm. Very good values for the transmission and resistivity are obtained.
- the powder of Comparison Example 4 in which the oxidation takes place above the boiling temperature of the zinc powder, has a mean maximum aggregate diameter markedly higher than 300 nm.
- the resulting values for transmission and resistivity are markedly above those of the powders according to the invention of Examples 1 to 3.
- Example 5 describes the preparation of an undoped zinc oxide powder, which is obtained by oxidation below the boiling temperature of zinc.
- the transmission of that powder is comparable with that of the powders according to the invention, but its resistivity is markedly higher.
- Table 1 Process parameters
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT03740427T ATE486815T1 (en) | 2002-08-05 | 2003-07-07 | DOPED ZINC OXIDE POWDER, METHOD FOR THE PRODUCTION AND USE THEREOF |
DE60334802T DE60334802D1 (en) | 2002-08-05 | 2003-07-07 | Doped zinc oxide powder, process for its preparation and use |
EP03740427A EP1527017B1 (en) | 2002-08-05 | 2003-07-07 | Doped zinc oxide powder, process for its preparation, and its use |
US10/522,778 US7235298B2 (en) | 2002-08-05 | 2003-07-07 | Doped zinc oxide powder, process for its preparation, and its use |
AU2003282117A AU2003282117B2 (en) | 2002-08-05 | 2003-07-07 | Doped zinc oxide powder, process for its preparation, and its use |
CA002494768A CA2494768C (en) | 2002-08-05 | 2003-07-07 | Doped zinc oxide powder, process for its preparation, and its use |
JP2004526723A JP4338638B2 (en) | 2002-08-05 | 2003-07-07 | Doped zinc oxide powder, process for its production and use thereof |
Applications Claiming Priority (2)
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---|---|---|---|
DE10235758.7 | 2002-08-05 | ||
DE10235758A DE10235758A1 (en) | 2002-08-05 | 2002-08-05 | Doped zinc oxide powder in aggregate form for use in e.g. electrically conductive lacquers and coatings, comprises doping component, e.g. aluminum oxide |
Publications (1)
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WO2004014800A1 true WO2004014800A1 (en) | 2004-02-19 |
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PCT/EP2003/007247 WO2004014800A1 (en) | 2002-08-05 | 2003-07-07 | Doped zinc oxide powder, process for its preparation, and its use |
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US (1) | US7235298B2 (en) |
EP (1) | EP1527017B1 (en) |
JP (1) | JP4338638B2 (en) |
KR (1) | KR100991038B1 (en) |
CN (1) | CN100360422C (en) |
AT (1) | ATE486815T1 (en) |
AU (1) | AU2003282117B2 (en) |
CA (1) | CA2494768C (en) |
DE (2) | DE10235758A1 (en) |
WO (1) | WO2004014800A1 (en) |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008015056A1 (en) * | 2006-07-29 | 2008-02-07 | Evonik Degussa Gmbh | Oxide particles comprising zinc and manganese |
WO2008128821A1 (en) * | 2007-04-19 | 2008-10-30 | Evonik Degussa Gmbh | Layers composite comprising a pyrogenic zinc oxide layer and field-effect transistor comprising this composite |
US8907333B2 (en) | 2007-04-19 | 2014-12-09 | Evonik Degussa Gmbh | Pyrogenic zinc oxide-comprising composite of layers and field-effect transistor comprising this composite |
FR2934705A1 (en) * | 2008-07-29 | 2010-02-05 | Univ Toulouse | ELECTRICALLY CONDUCTIVE COMPOSITE SOLID MATERIAL AND METHOD FOR OBTAINING SUCH MATERIAL |
US11446221B2 (en) | 2017-06-12 | 2022-09-20 | Sakai Chemical Industry Co., Ltd. | Trivalent metal-doped hexagonal plate-shaped zinc oxide and method for producing same |
Also Published As
Publication number | Publication date |
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US7235298B2 (en) | 2007-06-26 |
DE60334802D1 (en) | 2010-12-16 |
CA2494768C (en) | 2009-10-13 |
JP4338638B2 (en) | 2009-10-07 |
US20060073092A1 (en) | 2006-04-06 |
EP1527017B1 (en) | 2010-11-03 |
DE10235758A1 (en) | 2004-02-26 |
ATE486815T1 (en) | 2010-11-15 |
AU2003282117A1 (en) | 2004-02-25 |
AU2003282117B2 (en) | 2008-09-11 |
CN1675132A (en) | 2005-09-28 |
KR20050067135A (en) | 2005-06-30 |
CN100360422C (en) | 2008-01-09 |
CA2494768A1 (en) | 2004-02-19 |
KR100991038B1 (en) | 2010-10-29 |
JP2005534607A (en) | 2005-11-17 |
EP1527017A1 (en) | 2005-05-04 |
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