CN112624182B - Antistatic material and preparation method and application thereof - Google Patents
Antistatic material and preparation method and application thereof Download PDFInfo
- Publication number
- CN112624182B CN112624182B CN202011473243.9A CN202011473243A CN112624182B CN 112624182 B CN112624182 B CN 112624182B CN 202011473243 A CN202011473243 A CN 202011473243A CN 112624182 B CN112624182 B CN 112624182B
- Authority
- CN
- China
- Prior art keywords
- tin oxide
- grinding
- antimony
- antistatic material
- yttrium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G19/00—Compounds of tin
- C01G19/02—Oxides
-
- 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
- C04B35/453—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 zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates
- C04B35/457—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 zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates based on tin oxides or stannates
-
- 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
- C04B35/62605—Treating the starting powders individually or as mixtures
-
- 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
- C09K3/16—Anti-static materials
-
- 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
-
- 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
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
Abstract
The invention relates to the technical field of ceramic materials, and discloses an anti-static material, a preparation method and application thereof, wherein the anti-static material comprises the following raw material components: tin oxide, antimony trichloride and seed crystals; the seed crystal is nanometer powder of antimony doped tin oxide. The antistatic material has low resistivity and good antistatic property, the antimony-doped tin oxide is promoted to be formed by adopting the nano powder introduced with the antimony-doped tin oxide as the seed crystal and inducing the seed crystal, so that the yield of the product is improved, and meanwhile, the antimony can be uniformly attached to the surfaces of tin oxide particles by carrying out superfine grinding on the tin oxide and the antimony trichloride solution, so that the components of the final product are uniform and consistent.
Description
Technical Field
The invention relates to the technical field of ceramic materials, in particular to an anti-static material and a preparation method and application thereof.
Background
Static electricity is a common discharge phenomenon caused by friction in daily life, and the existence of potential static electricity on the surface of a material can cause potential safety hazards of some special environments such as laboratories, microcomputer rooms and the like. The tin antimony oxide (antimony doped tin oxide) powder has wide application prospect in many fields due to high conductivity, and is a novel antistatic functional material which is rapidly developed in recent years.
At present, the preparation method of the tin antimony oxide powder material mainly comprises a hydrothermal method, a chemical coprecipitation method and a solid phase method, but the hydrothermal method has high cost and is difficult to realize industrial production; the chemical coprecipitation method can generate more waste liquid, so that the environmental protection burden is increased; the solid phase method has slow reaction speed, is difficult to realize uniform mixing, and has low yield of the obtained tin antimony oxide.
Disclosure of Invention
The present invention is directed to an antistatic material, which solves one or more of the problems of the prior art and provides at least one of the advantages of the present invention.
The technical scheme adopted for solving the technical problems is as follows:
an antistatic material comprises the following raw material components: tin oxide, antimony trichloride and seed crystals; the seed crystal is nanometer powder of antimony doped tin oxide.
The seed crystal used in the invention is antimony doped tin oxide nano-powder synthesized by a water-based sol-gel method, and the water-based sol-gel method can be prepared by referring to a preparation method of antimony doped nano-tin oxide powder disclosed in patent CN 106564937A.
Preferably, the average particle size of the tin oxide is 5 to 15 micrometers; the mass of the seed crystal accounts for 0.5-2.5% of the mass of the material.
The second purpose of the present invention is to provide a method for preparing the above antistatic material, comprising the following steps:
1) Adding deionized water and a dispersing agent into the tin oxide, and grinding by adopting a medium stirring mill to obtain slurry A;
2) Adding water into the antimony trichloride, and stirring and fully dissolving to obtain an antimony trichloride solution;
3) Adding the seed crystal and the antimony trichloride solution into the slurry A at the same time, and grinding by adopting a high-medium stirring mill to obtain slurry B;
4) Carrying out spray drying on the slurry B to obtain powder;
5) And sequentially calcining the powder at high temperature, cooling to room temperature, crushing, and sieving with a 200-325-mesh sieve to obtain the antistatic material.
Preferably, in the step 1), the dispersant is polyethylene glycol with the molecular weight of 8000-10000, and the mass of the polyethylene glycol accounts for 0.8-1.2% of that of the tin oxide.
Preferably, in step 1), the solid content of the slurry A is 60 to 65 percent.
Preferably, in the step 1), the grinding is carried out by taking yttrium-stabilized zirconia balls as grinding media; wherein the average grain diameter of the yttrium-stabilized zirconia balls is 0.3-0.5 mm, the filling rate of the yttrium-stabilized zirconia balls is 65-70%, the grinding speed is more than or equal to 2000 r/min, and the grinding time is 1-2 hours.
Preferably, in the step 3), the grinding is specifically carried out by using yttrium-stabilized zirconia balls as grinding media; wherein the average grain diameter of the yttrium-stabilized zirconia balls is 0.3-0.5 mm, the filling rate of the yttrium-stabilized zirconia balls is 72-75%, the grinding speed is greater than or equal to 3000 r/min, and the grinding time is 1-1.5 hours.
Preferably, in the step 4), the temperature of the hot air for spray drying is 140-160 ℃.
Preferably, in the step 5), the calcining temperature is 600-800 ℃, and the calcining time is 2-4 hours.
The third purpose of the invention is to provide the application of the antistatic material in the ceramic material.
Compared with the prior art, the invention has the following beneficial effects:
1. the antistatic material has low resistivity and good antistatic property.
2. The invention adopts the nanometer powder body introduced with the antimony doped tin oxide as the seed crystal, promotes the formation of the antimony doped tin oxide through the induction of the seed crystal, and improves the yield of the product.
3. According to the invention, the tin oxide and antimony trichloride solution are subjected to superfine grinding, so that antimony can be uniformly attached to the surfaces of tin oxide particles, and the components of a final product are uniform and consistent.
4. The invention adopts the steps of superfine grinding, coarse grinding of coarse particles and fine grinding of fine particles to the raw materials, which is beneficial to improving the grinding efficiency, so that the material components are mixed more uniformly, and the product quality is more stable.
5. The preparation method is simple and easy to industrialize.
Detailed Description
The concept and technical effects of the present invention will be clearly and completely described below in conjunction with the embodiments to fully understand the objects, features and effects of the present invention. It is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments, and those skilled in the art can obtain other embodiments without inventive effort based on the embodiments of the present invention, and all embodiments are within the protection scope of the present invention.
Example 1
An antistatic material comprises the following raw material components: the tin oxide-antimony trichloride crystal seed comprises tin oxide, antimony trichloride and a crystal seed, wherein the crystal seed is antimony-doped tin oxide nano-powder, and the average particle size of the tin oxide is 5-15 micrometers; the mass of the seed crystal accounts for 0.5-2.5% of the mass of the material.
The preparation method of the antistatic material comprises the following steps:
1) Weighing 147.70 g of tin oxide with the average particle size of 5 micrometers, adding 100 ml of deionized water and 1.77 g of polyethylene glycol-10000, grinding by adopting a medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 65%, adjusting the rotating speed of the medium stirring mill to 2000 r/min, and grinding for 1 hour to obtain slurry A;
2) Weighing 9.12 g of antimony trichloride, adding water, stirring and fully dissolving to obtain an antimony trichloride solution;
3) Weighing 0.77 g of antimony-doped tin oxide nano powder, simultaneously adding the antimony-doped tin oxide nano powder and an antimony trichloride solution into the slurry A, and grinding by adopting a high-medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 75%, the rotating speed of the medium stirring mill is adjusted to 3000 r/min, and grinding is carried out for 1.0 hour to obtain slurry B;
4) Spray drying the slurry B, and setting the hot air temperature of the spray drying to be 150 ℃ to obtain powder;
5) Calcining the powder at the high temperature of 600 ℃ for 2 hours, cooling to room temperature, crushing, and sieving with a 200-325-mesh sieve.
Example 2
An antistatic material comprises the following raw material components: the tin oxide-antimony trichloride crystal seed comprises tin oxide, antimony trichloride and a crystal seed, wherein the crystal seed is antimony-doped tin oxide nano-powder, and the average particle size of the tin oxide is 5-15 micrometers; the mass of the seed crystal accounts for 0.5-2.5% of the mass of the material.
The preparation method of the antistatic material comprises the following steps:
1) Weighing 135.64 g of tin oxide with the average particle size of 15 micrometers, adding 100 ml of deionized water and 1.08 g of polyethylene glycol-10000, grinding by adopting a medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 70%, adjusting the rotating speed of the medium stirring mill to 2200 rpm, and grinding for 2 hours to obtain slurry A;
2) Weighing 27.37 g of antimony trichloride, adding water, stirring and fully dissolving to obtain an antimony trichloride solution;
3) Weighing 3.83 g of antimony-doped tin oxide nano powder, simultaneously adding the antimony-doped tin oxide nano powder and an antimony trichloride solution into the slurry A, and grinding by adopting a high-medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.3 mm, the filling rate of the yttrium-stabilized zirconia ball is 72%, the rotating speed of the medium stirring mill is adjusted to 3100 r/min, and grinding is carried out for 1.5 hours to obtain slurry B;
4) Spray drying the slurry B, and setting the hot air temperature of the spray drying to be 150 ℃ to obtain powder;
5) Calcining the powder at the high temperature of 800 ℃ for 4 hours, cooling to room temperature, crushing, and sieving with a 200-325-mesh sieve.
Example 3
An antistatic material comprises the following raw material components: the tin oxide-antimony trichloride crystal seed comprises tin oxide, antimony trichloride and a crystal seed, wherein the crystal seed is antimony-doped tin oxide nano-powder, and the average particle size of the tin oxide is 5-15 micrometers; the mass of the seed crystal accounts for 0.5-2.5% of the mass of the material.
The preparation method of the antistatic material comprises the following steps:
1) Weighing 141.25 g of tin oxide with the average particle size of 12 microns, adding 100 ml of deionized water and 1.52 g of polyethylene glycol-10000, grinding by adopting a medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 68%, adjusting the rotating speed of the medium stirring mill to 2200 rpm, and grinding for 1.5 hours to obtain slurry A;
2) Weighing 14.55 g of antimony trichloride, adding water, stirring and fully dissolving to obtain an antimony trichloride solution;
3) Weighing 1.78 g of antimony-doped tin oxide nano powder, simultaneously adding the antimony-doped tin oxide nano powder and an antimony trichloride solution into the slurry A, and grinding by adopting a high-medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.3 mm, the filling rate of the yttrium-stabilized zirconia ball is 72%, the rotating speed of the medium stirring mill is adjusted to 3000 r/min, and grinding is carried out for 1.5 hours to obtain slurry B;
4) Spray drying the slurry B, and setting the hot air temperature of the spray drying to be 150 ℃ to obtain powder;
5) Calcining the powder at the high temperature of 750 ℃ for 3 hours, cooling to room temperature, crushing, and sieving with a 200-325-mesh sieve.
Example 4
An antistatic material comprises the following raw material components: the tin oxide-antimony trichloride crystal seed comprises tin oxide, antimony trichloride and a crystal seed, wherein the crystal seed is antimony-doped tin oxide nano-powder, and the average particle size of the tin oxide is 5-15 micrometers; the mass of the seed crystal accounts for 0.5-2.5% of the mass of the material.
The preparation method of the antistatic material comprises the following steps:
1) Weighing 145.27 g of tin oxide with the average particle size of 15 micrometers, adding 100 ml of deionized water and 1.08 g of polyethylene glycol-10000, grinding by adopting a medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 70%, adjusting the rotating speed of the medium stirring mill to 2000 r/min, and grinding for 1 hour to obtain slurry A;
2) Weighing 15.46 g of antimony trichloride, adding water, stirring and fully dissolving to obtain an antimony trichloride solution;
3) Weighing 2.71 g of antimony-doped tin oxide nano powder, simultaneously adding the antimony-doped tin oxide nano powder and an antimony trichloride solution into the slurry A, and grinding by adopting a high-medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.3 mm, the filling rate of the yttrium-stabilized zirconia ball is 75%, the rotating speed of the medium stirring mill is adjusted to 3500 rpm, and grinding is carried out for 1.5 hours to obtain slurry B;
4) Spray drying the slurry B, and setting the hot air temperature of the spray drying to be 150 ℃ to obtain powder;
5) Calcining the powder material at the high temperature of 600 ℃ for 4 hours, cooling to room temperature, crushing, and sieving by a 200-325-mesh sieve.
Comparative example 1 (different from example 1 in that no seed crystal was added)
An antistatic material comprises the following raw material components: the tin oxide and the antimony trichloride, wherein the average particle size of the tin oxide is 5-15 microns.
The preparation method of the antistatic material comprises the following steps:
1) Weighing 147.70 g of tin oxide with the average particle size of 5 micrometers, adding 100 ml of deionized water and 1.77 g of polyethylene glycol-10000, grinding by adopting a medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 65%, adjusting the rotating speed of the medium stirring mill to 2000 r/min, and grinding for 1 hour to obtain slurry A;
2) Weighing 9.12 g of antimony trichloride, adding water, stirring and fully dissolving to obtain an antimony trichloride solution;
3) Adding an antimony trichloride solution into the slurry A, and grinding by adopting a high-medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 75%, the rotating speed of the medium stirring mill is adjusted to 3000 r/min, and grinding is carried out for 1.0 hour to obtain a slurry B;
4) Spray drying the slurry B, and setting the hot air temperature of the spray drying to be 150 ℃ to obtain powder;
5) Calcining the powder at the high temperature of 600 ℃ for 2 hours, cooling to room temperature, crushing, and sieving with a 200-325-mesh sieve.
Comparative example 2 (difference from example 1 in that liquid antimony trichloride was replaced with solid antimony trioxide)
An antistatic material comprises the following raw material components: the tin oxide crystal seed comprises tin oxide, antimony trioxide and a crystal seed, wherein the crystal seed is antimony doped tin oxide nano powder, and the average particle size of the tin oxide is 5-15 micrometers; the mass of the seed crystal accounts for 0.5-2.5% of the mass of the material.
The preparation method of the antistatic material comprises the following steps:
1) Weighing 147.70 g of tin oxide with the average particle size of 5 micrometers, adding 100 ml of deionized water and 1.77 g of polyethylene glycol-10000, grinding by adopting a medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 65%, adjusting the rotating speed of the medium stirring mill to 2000 r/min, and grinding for 1 hour to obtain slurry A;
2) Weighing 9.12 g of antimony trioxide;
3) Weighing 0.77 g of antimony-doped tin oxide nano powder, simultaneously adding the antimony-doped tin oxide nano powder and antimony trioxide into the slurry A, and grinding by adopting a high-medium stirring mill, wherein the average particle size of a grinding medium yttrium-stabilized zirconia ball is 0.5 mm, the filling rate of the yttrium-stabilized zirconia ball is 75%, the rotating speed of the medium stirring mill is adjusted to 3000 r/min, and grinding is carried out for 1.0 hour to obtain slurry B;
4) Spray drying the slurry B, and setting the hot air temperature of the spray drying to be 150 ℃ to obtain powder;
5) Calcining the powder at the high temperature of 600 ℃ for 2 hours, cooling to room temperature, crushing, and sieving with a 200-325-mesh sieve.
Comparative example 3 (difference from example 1 in that conventional ball milling was used and milling was not carried out stepwise)
An antistatic material comprises the following raw material components: the tin oxide-antimony trichloride crystal seed comprises tin oxide, antimony trichloride and a crystal seed, wherein the crystal seed is antimony-doped tin oxide nano-powder, and the average particle size of the tin oxide is 5-15 micrometers; the mass of the seed crystal accounts for 0.5-2.5% of the mass of the material.
The preparation method of the antistatic material comprises the following steps:
1) Weighing 147.70 g of tin oxide with the average particle size of 5 microns, weighing 9.12 g of antimony trichloride, weighing 0.77 g of antimony doped tin oxide nano-powder, adding 100 ml of deionized water and 1.77 g of polyethylene glycol-10000, and grinding for 2.5 hours by adopting a common ceramic ball mill to obtain slurry;
2) Spray drying the slurry, wherein the hot air temperature of the spray drying is set to be 150 ℃, so as to obtain powder;
3) Calcining the powder at the high temperature of 600 ℃ for 2 hours, cooling to room temperature, crushing, and sieving with a 200-325-mesh sieve.
The antistatic materials obtained in examples 1 to 4 and comparative examples 1 to 3 were subjected to a performance test:
60 g of the antistatic materials prepared in the embodiments 1-4 and the comparative examples 1-3 are respectively weighed, a wafer with the diameter (D) of 10 mm and a certain thickness (H) is prepared under the pressure of 5000N, copper sheets are arranged on two ends of the wafer, a probe of a resistance instrument is directly contacted with the copper sheets to test the resistance (R), and the resistivity (rho) is obtained through a calculation formula: resistivity = π RD 2 and/4H. The calculation results are shown in table 1 below.
TABLE 1
Test sample | Resistivity (ohm/cm) |
Example 1 | 1.25 |
Example 2 | 0.89 |
Example 3 | 2.55 |
Example 4 | 2.27 |
Comparative example 1 | 6.48 |
Comparative example 2 | 5.97 |
Comparative example 3 | 10.81 |
As can be seen from the data in Table 1, the resistivity of the antistatic materials prepared in the examples 1 to 4 of the present invention is between 0.8 and 2.6, which is lower than that of the antistatic materials prepared in the comparative examples 1 to 3, and thus the antistatic properties of the antistatic materials prepared in the examples 1 to 4 of the present invention are better; comparative example 1 has low product yield due to no seed crystal added, thereby affecting antistatic performance; comparative example 2 because liquid antimony trichloride was replaced with solid antimony trioxide, antimony did not adhere uniformly to the surface of tin oxide particles, thereby affecting antistatic properties; comparative example 3 because the traditional ball milling mode is adopted, grinding is not carried out step by step, the materials are mixed unevenly, and the antistatic performance is influenced.
While the preferred embodiments of the present invention have been illustrated and described, it will be understood by those skilled in the art that the present invention is not limited to the details of the embodiments shown and described, but is capable of numerous modifications and substitutions without departing from the spirit of the present invention and within the scope of the appended claims.
Claims (9)
1. The antistatic material is characterized by comprising the following raw material components: tin oxide, antimony trichloride and seed crystals; the seed crystal is nanometer powder of antimony doped tin oxide;
the preparation method of the antistatic material comprises the following steps:
1) Adding water and a dispersing agent into the tin oxide, and grinding to obtain slurry A;
2) Adding water into the antimony trichloride, and stirring to obtain an antimony trichloride solution;
3) Adding the seed crystal and the antimony trichloride solution into the slurry A, and grinding to obtain slurry B;
4) Drying the slurry B to obtain powder;
5) And sequentially calcining, cooling, crushing and sieving the powder to obtain the antistatic material.
2. The antistatic material according to claim 1, wherein the average particle diameter of the tin oxide is 5 to 15 μm; the mass of the seed crystal accounts for 0.5-2.5% of the mass of the antistatic material.
3. The antistatic material of claim 1, wherein in the step 1), the dispersant is polyethylene glycol with a molecular weight of 8000-10000, and the mass of the polyethylene glycol accounts for 0.8-1.2% of the mass of the tin oxide.
4. The antistatic material of claim 1, wherein the solid content of the slurry A in the step 1) is 60-65%.
5. The antistatic material of claim 1, wherein in the step 1), the grinding is carried out by using yttrium-stabilized zirconia balls as grinding media; wherein the average grain diameter of the yttrium-stabilized zirconia balls is 0.3-0.5 mm, the filling rate of the yttrium-stabilized zirconia balls is 65-70%, the grinding speed is more than or equal to 2000 r/min, and the grinding time is 1-2 hours.
6. The antistatic material of claim 1, wherein in the step 3), the grinding is carried out by using yttrium-stabilized zirconia balls as grinding media; wherein the average grain diameter of the yttrium-stabilized zirconia balls is 0.3-0.5 mm, the filling rate of the yttrium-stabilized zirconia balls is 72-75%, the grinding speed is greater than or equal to 3000 r/min, and the grinding time is 1-1.5 hours.
7. The antistatic material of claim 1, wherein the temperature of the hot air for drying in step 4) is 140 to 160 ℃.
8. The antistatic material of claim 1, wherein in the step 5), the calcination temperature is 600 to 800 ℃ and the calcination time is 2 to 4 hours.
9. Use of an antistatic material according to any one of claims 1 to 8 in a ceramic material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011473243.9A CN112624182B (en) | 2020-12-15 | 2020-12-15 | Antistatic material and preparation method and application thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011473243.9A CN112624182B (en) | 2020-12-15 | 2020-12-15 | Antistatic material and preparation method and application thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN112624182A CN112624182A (en) | 2021-04-09 |
CN112624182B true CN112624182B (en) | 2023-03-31 |
Family
ID=75312691
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202011473243.9A Active CN112624182B (en) | 2020-12-15 | 2020-12-15 | Antistatic material and preparation method and application thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN112624182B (en) |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101643200A (en) * | 2009-08-31 | 2010-02-10 | 石家庄铁道学院 | Preparation method of antimony-doped tin oxide nano-powder |
CN102010197A (en) * | 2010-09-29 | 2011-04-13 | 大连交通大学 | Method for preparing antimony-doped tin oxide (ATO) nano powder |
CN103318951A (en) * | 2013-07-10 | 2013-09-25 | 赵宝勤 | Preparation method of ATO (Antimony doped Tin Oxide) nanopowder |
WO2014029005A1 (en) * | 2012-08-22 | 2014-02-27 | Hy-Power Nano Inc. | Method for continuous preparation of indium-tin coprecipitates and indium-tin-oxide nanopowders with substantially homogeneous indium/tin composition, controllable shape and particle size |
CN106986376A (en) * | 2017-04-27 | 2017-07-28 | 柳州豪祥特科技有限公司 | Nano ATO raw powder's production technology |
CN107140687A (en) * | 2017-06-23 | 2017-09-08 | 广州特种承压设备检测研究院 | A kind of compound nuclear shell structure nano powder |
CN107162044A (en) * | 2017-06-23 | 2017-09-15 | 广州特种承压设备检测研究院 | A kind of compound nuclear shell structure nano powder preparation method |
-
2020
- 2020-12-15 CN CN202011473243.9A patent/CN112624182B/en active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101643200A (en) * | 2009-08-31 | 2010-02-10 | 石家庄铁道学院 | Preparation method of antimony-doped tin oxide nano-powder |
CN102010197A (en) * | 2010-09-29 | 2011-04-13 | 大连交通大学 | Method for preparing antimony-doped tin oxide (ATO) nano powder |
WO2014029005A1 (en) * | 2012-08-22 | 2014-02-27 | Hy-Power Nano Inc. | Method for continuous preparation of indium-tin coprecipitates and indium-tin-oxide nanopowders with substantially homogeneous indium/tin composition, controllable shape and particle size |
CN103318951A (en) * | 2013-07-10 | 2013-09-25 | 赵宝勤 | Preparation method of ATO (Antimony doped Tin Oxide) nanopowder |
CN106986376A (en) * | 2017-04-27 | 2017-07-28 | 柳州豪祥特科技有限公司 | Nano ATO raw powder's production technology |
CN107140687A (en) * | 2017-06-23 | 2017-09-08 | 广州特种承压设备检测研究院 | A kind of compound nuclear shell structure nano powder |
CN107162044A (en) * | 2017-06-23 | 2017-09-15 | 广州特种承压设备检测研究院 | A kind of compound nuclear shell structure nano powder preparation method |
Non-Patent Citations (1)
Title |
---|
非均相成核法制备ATO纳米粉末及其性能;李历历等;《稀有金属材料与工程》;20060331;第441-446页 * |
Also Published As
Publication number | Publication date |
---|---|
CN112624182A (en) | 2021-04-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100409979C (en) | Production of nano-SiO2 for coating carbonyl iron powder | |
CN101134597B (en) | ITO powder and method for manufacturing same, coating material for electroconductive ITO film, and transparent electroconductive film | |
CN105236941A (en) | Aluminum oxide anti-static ceramic material and preparation method thereof | |
JP2007070188A (en) | Method for producing zinc oxide fine particle and aggregate and dispersion solution of the same | |
CN101805517A (en) | Manufacturing method of inorganic particle filled polyimide film | |
CN101200004A (en) | Chemical preparing process for flake micron silver powder | |
CN101569936A (en) | Preparation method for flaky micro-aluminum powder | |
CN115745573A (en) | Preparation method of fine-grain IZO target material | |
CN112624182B (en) | Antistatic material and preparation method and application thereof | |
JP2010180471A (en) | Flaky silver powder and method for producing the same, and conductive paste | |
CN101323672B (en) | Corona-resistant polyimide film and preparing method thereof | |
CN104263056B (en) | The preparation method of tin-antiomony oxide organic nano slurry | |
CN103896249B (en) | Spherical Carbon nanotube group and its production and use | |
CN103722175A (en) | Method for manufacturing superfine flaky zinc powder with high corrosion resistance | |
CN107610852B (en) | A kind of thick film resistor composition and preparation method thereof | |
KR20180047527A (en) | Surface treated silver powder and manufacturing method of the same | |
KR20180078208A (en) | Surface treated silver powder and manufacturing method of the same | |
CA2034106C (en) | Process for fabricating doped zinc oxide microspheres | |
JPH0788391A (en) | Production of superfine powder | |
JPH01294792A (en) | Magnesium hydroxide flame retarder and production thereof | |
Fu et al. | Surface charge tuning of ceria particles by titanium doping: Towards significantly improved polishing performance | |
TW201537586A (en) | A conductive paste composition for forming conductive thin film on a flexible substrate and a method for producing the same | |
CN115893461A (en) | Production process of nano aluminum oxide polishing powder | |
JPH07330337A (en) | Dispersion of electro-conductive fine powder and its production | |
Ye et al. | Improving the Dispersion Stability and Chemical Mechanical Polishing Performance of CeO2 Slurries |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |