Method of preparing silicon carbide powder comprising converting a liquid SiC precursor to a B-phase SiC particulate material
09551086 ยท 2017-01-24
Assignee
Inventors
Cpc classification
C01B32/977
CHEMISTRY; METALLURGY
C04B35/62675
CHEMISTRY; METALLURGY
C04B35/62645
CHEMISTRY; METALLURGY
C04B2235/72
CHEMISTRY; METALLURGY
C04B2235/48
CHEMISTRY; METALLURGY
C04B35/65
CHEMISTRY; METALLURGY
C30B7/14
CHEMISTRY; METALLURGY
C04B2235/483
CHEMISTRY; METALLURGY
B22F2304/10
PERFORMING OPERATIONS; TRANSPORTING
Y10T428/2982
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
C04B2235/5445
CHEMISTRY; METALLURGY
B22F1/142
PERFORMING OPERATIONS; TRANSPORTING
C04B2235/5436
CHEMISTRY; METALLURGY
C30B1/10
CHEMISTRY; METALLURGY
B22F1/05
PERFORMING OPERATIONS; TRANSPORTING
International classification
B22F1/00
PERFORMING OPERATIONS; TRANSPORTING
C30B1/10
CHEMISTRY; METALLURGY
C30B7/14
CHEMISTRY; METALLURGY
C04B35/626
CHEMISTRY; METALLURGY
C04B35/628
CHEMISTRY; METALLURGY
C04B35/65
CHEMISTRY; METALLURGY
Abstract
A method of preparing silicon carbide powder is provided, which includes mixing first silicon carbide powder with a liquid silicon carbide precursor, annealing the mixture at a first temperature and converting the silicon carbide precursor to a -phase silicon carbide particulate material, and annealing the material at a second temperature and grain-growing the first silicon carbide powder to second silicon carbide powder using the -phase silicon carbide particulate material.
Claims
1. A method of preparing silicon carbide powder, comprising: mixing first silicon carbide powder with a liquid silicon carbide precursor; annealing the mixture at a first temperature, and converting the silicon carbide precursor to -phase silicon carbide particulate material; and annealing the material at a second temperature, and grain-growing the first silicon carbide powder to second silicon carbide powder using the -phase silicon carbide particulate material.
2. The method according to claim 1, wherein the first silicon carbide powder has a particle size (D50) of 0.2 to 9 m.
3. The method according to claim 1, wherein the second silicon carbide powder has a dispersion (D90/D10) of 1 to 10 and a particle size (D50) of 40 to 150 m, and is in phase.
4. The method according to claim 3, wherein the second silicon carbide powder has impurities of 0.1 to 10 ppm.
5. The method according to claim 1, wherein the silicon carbide precursor includes at least one selected from the group consisting of silazane and polycarbosilane.
6. The method according to claim 1, wherein the silicon carbide precursor is added at 5 to 20 wt % with respect to a total weight of the first silicon carbide powder and the silicon carbide precursor.
7. The method according to claim 1, wherein the silicon carbide precursor includes silicon carbide preceramic polymer series.
8. The method according to claim 1, wherein the first temperature and the second temperature are 2000 C. or less.
9. The method according to claim 8, wherein the first temperature is 1500 C. to 1600 C.
10. The method according to claim 1, wherein the -phase silicon carbide particulate material is smaller than the particle size (D50) of the first silicon carbide powder.
11. The method according to claim 10, wherein the -phase silicon carbide particulate material has a nm unit particle size and is in a solid phase.
12. The method according to claim 1, wherein a particle size of the second silicon carbide powder is controlled according to annealing time at the second temperature.
13. The method according to claim 1, wherein the mixing comprises coating a surface of the first silicon carbide powder with the liquid silicon carbide precursor.
14. The method according to claim 13, wherein an organic solvent is used for the coating.
Description
BRIEF DESCRIPTION OF DRAWINGS
(1)
(2)
MODE FOR THE INVENTION
(3) The present invention will be modified in various forms and have several exemplary embodiments, but only specific embodiments are to be described with reference to drawings. However, it could be understood that the present invention is not limited to specific embodiments disclosed below, but includes all of modifications, equivalents or substitutions in the scope and technical range of the present invention.
(4) Although the terms first, second, etc. may be used to describe various elements, these elements are not limited by these terms. These terms are only used to distinguish one element from another. For example, a first element could be termed a second element, and, similarly, a second element could be termed a first element, without departing from the scope of exemplary embodiments. The term and/or includes any and all combinations of one or more of the associated listed items.
(5) The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of exemplary embodiments. The singular forms a, an and the are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms comprises, comprising, includes and/or including, when used herein, specify the presence of stated features, integers, steps, operations, elements, components and/or groups thereof, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components and/or groups thereof.
(6) Unless defined otherwise, all of terminology used herein, including technical or scientific terms, has the same meanings as those generally understood by one of ordinary skill in the art to which the present invention belongs. Such terms defined in generally used dictionaries are to be interpreted as having meanings equivalent to the contextual meanings in the related art, and not to be interpreted as having ideal or excessively formal meanings unless clearly defined in the specification.
(7) With reference to the appended drawings, exemplary embodiments of the present invention will be described in detail below. To aid in understanding the present invention, like numbers refer to like elements throughout the description of the figures, and the description of the same elements will be not reiterated.
(8)
(9) Referring to
(10) First, referring to
(11) The fine silicon carbide powder 100 may be obtained by mixing a silicon source providing silicon and a carbon source providing carbon, and heating the mixture. The silicon source may be at least one selected from the group consisting of, for example, fumed silica, silica sol, silica gel, fine silica, quartz powder and a mixture thereof. The solid carbon source may be, for example, at least one selected from the group consisting of graphite, carbon black, carbon nanotubes (CNT), fullerenes and a mixture thereof. An organic carbon compound may be at least one selected from the group consisting of a phenol resin, a franc resin, a xylene resin, polyimide, polyurethane, polyvinyl alcohol, polyacrylonitrile, polyvinyl acetate, cellulose and a mixture thereof. To obtain the fine silicon carbide powder 100, the mixed silicon source and carbon source may be heated at 1700 to 1800 C.
(12) Meanwhile, as shown in
(13) Here, the silicon carbide precursor 210 may include silicon carbide preceramic polymer series. As an example, the silicon carbide precursor 210 may include silazane or polycarbosilane.
(14) The fine silicon carbide powder 100 and the silicon carbide precursor 210 may be mixed using, for example, a ball mill, a spray dry or a Henschel mixer.
(15) In addition, to coat the silicon carbide precursor 210, an organic solvent such as ethanol or isopropylantipyrine (IPA) may be used.
(16) The silicon carbide precursor 210 may be added at 5 to 20 wt % with respect to a total weight of the fine silicon carbide powder 100 and the silicon carbide precursor 210. Such a weight of the silicon carbide precursor 210 is an amount for suitably coating a surface of the fine silicon carbide powder 100.
(17) Subsequently, referring to
(18) The silicon carbide precursor 210 may be thermally decomposed at 1600 C. or less, and thus converted to the -phase silicon carbide particulate material 220. Here, the -phase silicon carbide particulate material 220 may have a superfine (e.g., nm unit) particle size, and may be in a solid phase.
(19) Subsequently, referring to
(20) Meanwhile, the annealing may be maintained for 1 to 10 hours. As the annealing time is increased, silicon carbide powder having a high particle size may be obtained. Therefore, the particle size of the silicon carbide powder may be controlled using the annealing time.
(21) In addition, ST200 and ST300 may be continuously or intermittently performed. For example, as a temperature is slowly increased from 1500 to 2000 C., the conversion to a -phase silicon carbide particulate material (ST200) and the grain-growth of the silicon carbide powder (ST300) may be performed, or the conversion of a n-phase silicon carbide particulate material (ST200) may be performed at a temperature of 1600 C. or less, and then the grain growth of the silicon carbide powder (ST300) may be performed at an increased temperature.
(22) According to an exemplary embodiment of the present invention, as shown in
(23) While the invention has been shown and described with reference to certain exemplary embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention as defined by the appended claims.