Composite abrasive with hard core and soft shell, manufacturing method and application method
10577525 ยท 2020-03-03
Assignee
Inventors
- Jing LU (Quanzhou, CN)
- Xipeng XU (Quanzhou, CN)
- Dayu Zhang (Quanzhou, CN)
- Yongchao Xu (Quanzhou, CN)
- Qiufa LUO (Quanzhou, CN)
Cpc classification
C04B35/1115
CHEMISTRY; METALLURGY
C04B2235/3293
CHEMISTRY; METALLURGY
C04B2235/3229
CHEMISTRY; METALLURGY
C09K3/1445
CHEMISTRY; METALLURGY
C04B2235/3206
CHEMISTRY; METALLURGY
C04B35/62897
CHEMISTRY; METALLURGY
C04B2235/5445
CHEMISTRY; METALLURGY
B24B7/228
PERFORMING OPERATIONS; TRANSPORTING
International classification
B24B7/22
PERFORMING OPERATIONS; TRANSPORTING
C04B35/628
CHEMISTRY; METALLURGY
Abstract
Disclosed is a composite abrasive with hard core and soft shell, comprising hard abrasive core with grain diameter in a range of 0.11 m and a soft oxide shell with thickness in a range of 5100 nm, the grain size of the oxide of the soft oxide shell is in a range of 520 nm, the composite abrasive is obtained from aqueous solution of oxide inorganic salt precursor and the hard abrasive by dispersing, constant temperature reflux hydrolyzing, solid-liquid separating, washing and drying. The component abrasive with hard core and soft shell of the present invention can improve the manufacturing efficiency and the surface quality during the ultraprecise manufacturing of the sapphire substrate.
Claims
1. A manufacturing method of a composite abrasive with a hard abrasive core and a soft oxide shell, wherein comprising the steps: (1) preparing an aqueous solution of an oxide inorganic salt precursor with a concentration of 0.1-1 mol/L by dissolving the oxide inorganic salt precursor in deionized water, wherein an oxide of the oxide inorganic salt precursor is at least one SnO.sub.2, CeO.sub.2, MgO, FeO, or Fe.sub.2O.sub.3; (2) putting hard abrasive cores into the aqueous solution, wherein a mass concentration of the hard abrasive cores in the aqueous solution is in a range of 1-10%; (3) ultrasonic dispersing the material of step (2) for 10-15 minutes to obtain a stable emulsion; (4) reflux hydrolyzing the emulsion in a constant temperature of 60-90 C. for 8-72 hours; (5) solid-liquid separating the material of step (4), wherein a solid obtained from the solid-liquid separation is washed by distilled water and absolute ethyl alcohol; and (6) drying the solid of step (5) in 40-45 C. to obtain the composite abrasive with the hard abrasive core and the soft oxide shell.
2. The composite abrasive with the hard abrasive core and the soft oxide shell manufactured according to the manufacturing method of claim 1, wherein the hard abrasive core has a grain diameter in a range of 0.1-1 m and the soft oxide shell has a thickness in a range of 5-100 nm, a grain size of an oxide of the soft oxide shell is in a range of 5-20 nm.
3. The composite abrasive with the hard abrasive core and the soft oxide shell according to claim 2, wherein the hard abrasive core comprises at least one of diamond, cBN, B.sub.4C, SiC or Al.sub.2O.sub.3.
4. The composite abrasive with the hard abrasive core and the soft oxide shell according to claim 2, wherein the oxide of the soft oxide shell comprises at least one of SnO.sub.2, CeO.sub.2, MgO, FeO or Fe.sub.2O.sub.3.
5. The composite abrasive with the hard abrasive core and soft oxide shell according to claim 4, wherein an inorganic salt precursor of the oxide inorganic salt precursor comprises at least one of chlorine salt, nitrate or sulfate.
6. The manufacturing method according to claim 1, wherein in step (5), the material of step (4) is vacuum filtered, the solid is washed by distilled water 5 times and washed by absolute ethyl alcohol 3 times in turn.
7. The manufacturing method according to claim 1, wherein in step (6), a drying period for drying the solid of step (5) is 20-30 hours.
8. The manufacturing method according to claim 5, wherein the hard abrasive cores comprise at least one of diamonds, cBN, B.sub.4C, SiC or Al.sub.2O.sub.3.
9. The manufacturing method according to claim 8, wherein an inorganic salt precursor of the oxide inorganic salt precursor comprises at least one of chlorine salt, nitrate or sulfate.
10. The manufacturing method according to claim 8, wherein in step (5), the material of step (4) is vacuum filtered, the solid is washed by distilled water 5 times and washed by absolute ethyl alcohol 3 times in turn.
11. The manufacturing method according to claim 9, wherein in step (5), the material of step (4) is vacuum filtered, the solid is washed by distilled water 5 times and washed by absolute ethyl alcohol 3 times in turn.
12. The manufacturing method according to claim 8, wherein in step (6), a drying period for drying the solid of step (5) is 20-30 hours.
13. The manufacturing method according to claim 9, wherein in step (6), a drying period for drying the solid of step (5) is 20-30 hours.
14. The manufacturing method according to claim 1, wherein the hard abrasive cores have a grain diameter in a range of 0.1-1 m and the soft oxide shell has a thickness in a range of 5-100 nm, and a grain size of an oxide of the soft oxide shell is in a range of 5-20 nm.
15. The manufacturing method according to claim 8, wherein the hard abrasive cores have a grain diameter in a range of 0.1-1 m and the soft oxide shell has a thickness in a range of 5-100 nm, and a grain size of an oxide of the soft oxide shell is in a range of 5-20 nm.
16. The manufacturing method according to claim 9, wherein the hard abrasive cores have a grain diameter in a range of 0.1-1 m and the soft oxide shell has a thickness in a range of 5-100 nm, and a grain size of an oxide of the soft oxide shell is in a range of 5-20 nm.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3)
(4)
(5)
(6)
DETAILED DESCRIPTION OF THE EMBODIMENTS
(7) The present invention will be further described with the drawings and the embodiments.
The First Embodiment
(8) (1) preparing 300 mL of ferric oxide solution with concentration of 1 mol/L by solving ferric chloride in deionized water; (2) putting 4.5 g of W1 diamond abrasive into the ferric oxide solution, as figured in
(9) Above obtained composite abrasive with hard core and soft shell is applied in semisolidification flexible polishing tools to mechano-chemical polish sapphire wafer to obtain a sub-nanometer surface finish quality with Ra 0.8 nm, the before and after of the manufacturing are figured in
The Second Embodiment
(10) (1) preparing 200 mL of magnesium nitrate solution with concentration of 0.2 mol/L by solving magnesium nitrate in deionized water; (2) putting 2 g of W0.5 aluminum oxide abrasive into the magnesium nitrate solution; (3) ultrasonic dispersing the material of step (2) for 10 minutes to obtain stable emulsion; (4) the emulsion is reflux hydrolyzed in a constant temperature bath of 60 C. for 24 hours; (5) the material of step (4) is vacuum filtered, the obtained solid is washed by distilled water for 5 times and washed by absolute ethyl alcohol for 3 times in turn. (6) drying the solid of step (5) in 40 C. for 24 hours to obtain the composite abrasive with hard core and soft shell, as figured in
(11) Above obtained composite abrasive with hard core and soft shell is applied in semisolidification flexible polishing tools to mechano-chemical polish sapphire wafer, the surface roughness Ra of the polished sapphire is 0.6 nm.
The Third Embodiment
(12) (1) preparing 250 mL of ferrous sulfate solution with concentration of 0.2 mol/L by solving ferrous sulfate in deionized water; (2) putting 5 g of W0.25 cubic boron nitride abrasive into the ferrous sulfate solution; (3) ultrasonic dispersing the material of step (2) for 15 minutes to obtain stable emulsion; (4) the emulsion is reflux hydrolyzed in a constant temperature bath of 85 C. for 36 hours; (5) the material of step (4) is vacuum filtered, the obtained solid is washed by distilled water for 5 times and washed by absolute ethyl alcohol for 3 times in turn. (6) drying the solid of step (5) in 45 C. for 20 hours to obtain the composite abrasive with hard core and soft shell, as figured in
(13) Above obtained composite abrasive with hard core and soft shell is applied in semisolidification flexible polishing tools to mechano-chemical polish sapphire wafer, the surface roughness Ra of the polished sapphire is 0.4 nm.
The Fourth Embodiment
(14) (1) preparing 200 mL of cerous nitrate solution with concentration of 0.5 mol/L by solving cerous nitrate in deionized water; (2) putting 10 g of W0.5 boron carbide into the cerous nitrate solution; (3) ultrasonic dispersing the material of step (2) for 10 minutes to obtain stable emulsion; (4) the emulsion is reflux hydrolyzed in a constant temperature bath of 70 C. for 54 hours; (5) the material of step (4) is vacuum filtered, the obtained solid is washed by distilled water for 5 times and washed by absolute ethyl alcohol for 3 times in turn. (6) drying the solid of step (5) in 45 C. for 20 hours to obtain the composite abrasive with hard core and soft shell, as figured in
(15) Above obtained composite abrasive with hard core and soft shell is applied in semisolidification flexible polishing tools to mechano-chemical polish sapphire wafer, the surface roughness Ra of the polished sapphire is 0.9 nm.
The Fifth Embodiment
(16) (1) preparing 300 mL of stannic chloride solution with concentration of 1 mol/L by solving stannic chloride in deionized water; (2) putting 6 g of W1 silicon carbide into the stannic chloride solution; (3) ultrasonic dispersing the material of step (2) for 10 minutes to obtain stable emulsion; (4) the emulsion is reflux hydrolyzed in a constant temperature bath of 60 C. for 16 hours; (5) the material of step (4) is vacuum filtered, the obtained solid is washed by distilled water for 5 times and washed by absolute ethyl alcohol for 3 times in turn. (6) drying the solid of step (5) in 40 C. for 30 hours to obtain the composite abrasive with hard core and soft shell, as figured in
(17) Above obtained composite abrasive with hard core and soft shell is applied in semisolidification flexible polishing tools to mechano-chemical polish sapphire wafer, the surface roughness Ra of the polished sapphire is 1.3 nm.
(18) A person skilled in this field knows that regulating the components and the parameters within the scope described hereafter can also obtain the similar technical effects to the embodiments, this kind of regulation is still within the scope of the present invention.
(19) A composite abrasive with hard core and soft shell, comprising hard abrasive core with grain diameter in a range of 0.11 m and a soft oxide shell with thickness in a range of 5100 nm, the grain size of the oxide of the soft oxide shell is in a range of 520 nm.
(20) the composite abrasive is obtained from aqueous solution of oxide inorganic salt precursor and the hard abrasive by dispersing, constant temperature reflux hydrolyzing, solid-liquid separating, washing and drying.
(21) The hard abrasive core comprises at least one kind selected from diamond, cBN, B.sub.4C, SiC and Al.sub.2O.sub.3.
(22) The oxide comprises at least one kind selected from SnO.sub.2, CeO.sub.2, MgO, FeO and Fe.sub.2O.sub.3.
(23) The inorganic salt precursor comprises at least one kind selected from chlorine salt, nitrate and sulfate.
(24) A manufacturing method of the composite abrasive with hard core and soft shell, comprising the steps: (1) preparing aqueous solution of oxide inorganic salt precursor with concentration of 0.11 mol/L by solving the oxide inorganic salt precursor in deionized water; (2) putting hard abrasive into the aqueous solution, the mass concentration of the hard abrasive in the aqueous solution is in a range of 110%; (3) ultrasonic dispersing the material of step (2) for 1015 minutes to obtain stable emulsion; (4) the emulsion is reflux hydrolyzed in a constant temperature of 6090 C. for 872 hours; (5) the material of step (4) is solid-liquid separated, the solid is washed by distilled water and absolute ethyl alcohol; (6) drying the solid of step (5) in 4045 C. to obtain the composite abrasive with hard core and soft shell.
(25) Although the present invention has been described with reference to the preferred embodiments thereof for carrying out the patent for invention, it is apparent to those skilled in the art that a variety of modifications and changes may be made without departing from the scope of the patent for invention which is intended to be defined by the appended claims.