CN102492394A - Preparation method of hexagonal tabular nano-crystal corundum abrasive - Google Patents
Preparation method of hexagonal tabular nano-crystal corundum abrasive Download PDFInfo
- Publication number
- CN102492394A CN102492394A CN2011103687962A CN201110368796A CN102492394A CN 102492394 A CN102492394 A CN 102492394A CN 2011103687962 A CN2011103687962 A CN 2011103687962A CN 201110368796 A CN201110368796 A CN 201110368796A CN 102492394 A CN102492394 A CN 102492394A
- Authority
- CN
- China
- Prior art keywords
- corundum abrasive
- additive
- abrasive
- tabular
- preparation
- 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.)
- Pending
Links
- 229910052593 corundum Inorganic materials 0.000 title claims abstract description 41
- 239000010431 corundum Substances 0.000 title claims abstract description 41
- 238000002360 preparation method Methods 0.000 title claims description 8
- 239000002159 nanocrystal Substances 0.000 title description 3
- 239000000654 additive Substances 0.000 claims abstract description 30
- 230000000996 additive effect Effects 0.000 claims abstract description 20
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 15
- 239000003082 abrasive agent Substances 0.000 claims abstract description 12
- 229910004298 SiO 2 Inorganic materials 0.000 claims abstract description 5
- 239000000084 colloidal system Substances 0.000 claims description 12
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000012535 impurity Substances 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 238000000967 suction filtration Methods 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 238000007873 sieving Methods 0.000 claims description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- 238000001354 calcination Methods 0.000 claims description 2
- 238000001556 precipitation Methods 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims 1
- 238000005469 granulation Methods 0.000 claims 1
- 230000003179 granulation Effects 0.000 claims 1
- 239000002994 raw material Substances 0.000 abstract description 13
- 238000000034 method Methods 0.000 abstract description 5
- 239000000919 ceramic Substances 0.000 abstract description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 2
- 239000007791 liquid phase Substances 0.000 abstract description 2
- 239000002243 precursor Substances 0.000 abstract description 2
- 229910018626 Al(OH) Inorganic materials 0.000 description 22
- 239000007864 aqueous solution Substances 0.000 description 8
- 238000000227 grinding Methods 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- 239000002245 particle Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 4
- 230000001376 precipitating effect Effects 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000006061 abrasive grain Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
Landscapes
- Polishing Bodies And Polishing Tools (AREA)
Abstract
本发明公开了一种六方板状纳米晶刚玉磨料,原料组分及其重量百分比含量为:99.15~99.85% Al2(SO4)3·18H2O或者Al(NO3)3·9H2O,0.15~0.85%添加剂;所述添加剂的原料组分及其重量百分比含量为:0~50%纳米SiO2、0~45%Fe(NO3)3、0~30%Y(NO3)3、5~100%Ca(NO3)2、0~70%Mg(NO3)2和0~25%Cr(NO3)3。本发明采用液相法合成含铝前驱体,经高温煅烧制成六方板状纳米晶刚玉磨料,该刚玉磨料的硬度与现有的陶瓷刚玉磨料的硬度相当,而韧性要比现有的陶瓷刚玉磨料提高9~25%。The invention discloses a hexagonal plate-like nanocrystalline corundum abrasive. The raw material components and their weight percent content are: 99.15-99.85% Al 2 (SO 4 ) 3 18H 2 O or Al(NO 3 ) 3 9H 2 O , 0.15-0.85% additive; the raw material components and weight percentage content of the additive are: 0-50% nano-SiO 2 , 0-45% Fe(NO 3 ) 3 , 0-30% Y(NO 3 ) 3 , 5-100% Ca(NO 3 ) 2 , 0-70% Mg(NO 3 ) 2 and 0-25% Cr(NO 3 ) 3 . The invention adopts a liquid phase method to synthesize an aluminum-containing precursor, and is calcined at a high temperature to make a hexagonal plate-shaped nanocrystalline corundum abrasive. The hardness of the corundum abrasive is equivalent to that of the existing ceramic corundum abrasive, and the toughness is better than that of the existing ceramic corundum. Abrasives increased by 9 to 25%.
Description
技术领域 technical field
本发明涉及磨削加工工具,尤其涉及一种六方板状纳米晶刚玉磨料的制备方法。The invention relates to a grinding tool, in particular to a preparation method of a hexagonal plate-like nanocrystalline corundum abrasive.
背景技术 Background technique
磨削加工是精密加工的重要方式,随着科学技术的进步,新材料和难以加工材料的不断涌现,对磨削加工精度、加工效率和加工能力都提出了新的挑战。传统的磨料很多时候难以满足现代加工的需要,因此,迫切需要有适应不同磨削需求的新型磨料。Grinding is an important way of precision machining. With the advancement of science and technology, new materials and difficult-to-machine materials continue to emerge, which pose new challenges to grinding precision, processing efficiency and processing capacity. Traditional abrasives are often difficult to meet the needs of modern processing. Therefore, there is an urgent need for new abrasives that can meet different grinding needs.
纳米晶刚玉磨料颗粒由无数小纳米晶组成,不同于传统熔融法制备的刚玉磨料,结构上的差异必然带来性能和应用上的差异。纳米晶刚玉磨料与传统熔融法制备的大单晶刚玉磨料相比具有韧性好、自锐性好、磨粒锋利、砂轮耐用性好等优点,同时,可以通过控制纳米晶刚玉磨料纳米晶大小、形状等显微结构来调整其不同的性能和适应不同的磨削应用需要。Nanocrystalline corundum abrasive particles are composed of countless small nanocrystals, which are different from corundum abrasives prepared by traditional melting methods. The difference in structure will inevitably lead to differences in performance and application. Compared with the large single crystal corundum abrasive prepared by the traditional melting method, the nanocrystalline corundum abrasive has the advantages of good toughness, good self-sharpening, sharp abrasive grains, and good durability of the grinding wheel. At the same time, the nanocrystalline corundum abrasive can be controlled by controlling the nanocrystal size, Shape and other microstructures to adjust its different properties and adapt to different grinding application needs.
不同用途的刚玉磨料对韧性要求不同,而六方板状纳米氧化铝能显著提高其断裂韧性。因此,制备一种六方板状刚玉磨料是提高其韧性的有效途径。Corundum abrasives for different purposes have different toughness requirements, and hexagonal plate-shaped nano-alumina can significantly improve its fracture toughness. Therefore, preparing a hexagonal plate-shaped corundum abrasive is an effective way to improve its toughness.
发明内容 Contents of the invention
本发明的目的是提高现有磨料的韧性,提供一种能够显著提高其断裂韧性的六方板状纳米晶刚玉磨料及其制备方法。The purpose of the present invention is to improve the toughness of the existing abrasives, and provide a hexagonal plate-shaped nanocrystalline corundum abrasive capable of significantly improving its fracture toughness and a preparation method thereof.
本发明通过如下技术方案予以实现。The present invention is realized through the following technical solutions.
一种六方板状纳米晶刚玉磨料,原料组分及其重量百分比含量为:99.15~99.85%Al2(SO4)3·18H2O或者Al(NO3)3·9H2O,0.15~0.85%添加剂;A hexagonal plate-shaped nanocrystalline corundum abrasive, the raw material components and their weight percentages are: 99.15-99.85% Al 2 (SO 4 ) 3 18H 2 O or Al(NO 3 ) 3 9H 2 O, 0.15-0.85% %additive;
所述添加剂的原料组分及其重量百分比含量为:0~50%纳米SiO2、0~45%Fe(NO3)3、0~30%Y(NO3)3、5~100%Ca(NO3)2、0~70%Mg(NO3)2和0~25%Cr(NO3)3。The raw material components of the additive and their weight percentage contents are: 0-50% nanometer SiO 2 , 0-45% Fe(NO 3 ) 3 , 0-30% Y(NO 3 ) 3 , 5-100% Ca( NO 3 ) 2 , 0-70% Mg(NO 3 ) 2 and 0-25% Cr(NO 3 ) 3 .
六方板状纳米晶刚玉磨料的制备方法,具有如下步骤:The preparation method of the hexagonal plate-like nanocrystalline corundum abrasive has the following steps:
(1)将Al2(SO4)3·18H2O或Al(NO3)3·9H2O溶于水,待完全溶解后过滤去除杂质,配成0.1~0.6mol/L的Al3+溶液;(1) Dissolve Al 2 (SO 4 ) 3 18H 2 O or Al(NO 3 ) 3 9H 2 O in water, filter to remove impurities after complete dissolution, and prepare 0.1-0.6 mol/L Al 3+ solution;
(2)在步骤(1)的溶液中加入氨水并搅拌使其完全溶胶或沉淀化,再经过抽滤、洗涤工艺获得Al(OH)3凝胶;(2) Add ammonia water to the solution of step (1) and stir to make it completely sol or precipitate, and then obtain Al(OH) 3gel through suction filtration and washing process;
(3)按原料组分及其重量百分比含量为:99.15~99.85% Al2(SO4)3·18H2O或者Al(NO3)3·9H2O,0.15~0.85%添加剂的比例,将相应量添加剂加入到步骤(2)中的胶体中,并使添加剂分布均匀;(3) According to the content of the raw material components and their weight percentages: 99.15-99.85% Al 2 (SO 4 ) 3 ·18H 2 O or Al(NO 3 ) 3 ·9H 2 O, the ratio of 0.15-0.85% additives, the A corresponding amount of additives is added to the colloid in step (2), and the additives are evenly distributed;
(4)将步骤(3)含添加剂的Al(OH)3胶体干燥,再造粒并进行筛分和分级;(4) step (3) contains additive Al(OH) Colloid drying, regranulation and screening and classification;
(5)将步骤(4)已经进行筛分和分级的磨料在1150℃~1400℃煅烧,再进一步的过筛和分级,制得六方板状纳米晶刚玉磨料。(5) Calcining the sieved and classified abrasive in step (4) at 1150° C. to 1400° C., and then further sieving and grading to obtain a hexagonal plate-like nanocrystalline corundum abrasive.
所述步骤(2)的氨水为沉淀剂。The ammoniacal liquor of described step (2) is precipitation agent.
所述步骤(5)制得的六方板状纳米刚玉磨料的内部显微晶粒尺寸为40nm~2μm。The internal microscopic grain size of the hexagonal plate-shaped nano-corundum abrasive prepared in the step (5) is 40nm-2μm.
本发明的有益效果是,提供了一种能够显著提高磨料断裂韧性的六方板状纳米晶刚玉磨料及其制备方法,该刚玉磨料的硬度与现有的陶瓷刚玉磨料的硬度相当,而韧性要比现有的陶瓷刚玉磨料提高9~25%。The invention has the beneficial effects of providing a hexagonal plate-shaped nanocrystalline corundum abrasive capable of significantly improving the fracture toughness of the abrasive and a preparation method thereof. The hardness of the corundum abrasive is equivalent to that of the existing ceramic corundum abrasive, and the toughness is lower than The existing ceramic corundum abrasives are improved by 9-25%.
具体实施方式 Detailed ways
下面结合具体实施例对本发明作进一步描述。The present invention will be further described below in conjunction with specific embodiments.
氧化铝的磨削应用效果受其内部晶粒大小和形状的影响明显,磨料的细晶结构可以提高磨削精度,磨料的微观板状结构可以提高磨料的韧性。鉴于上述原因,本发明采用液相法合成含铝前驱体,再经高温煅烧而制备六方板状纳米晶刚玉磨料。The grinding application effect of alumina is obviously affected by the size and shape of its internal grains. The fine-grained structure of the abrasive can improve the grinding accuracy, and the microscopic plate-like structure of the abrasive can improve the toughness of the abrasive. In view of the above reasons, the present invention adopts a liquid phase method to synthesize an aluminum-containing precursor, and then calcines at a high temperature to prepare a hexagonal plate-like nanocrystalline corundum abrasive.
本发明采用市售的分析纯为原料。The present invention uses commercially available analytical pure as raw material.
实施例1Example 1
采用99.85%的Al(NO3)3·9H2O和0.15%的添加剂为原料,所述0.15%添加剂的原料组分及重量百分比含量为30%纳米SiO2、5%Y(NO3)3、10%Fe(NO3)3、26%Ca(NO3)2、14%Mg(NO3)2和15%Cr(NO3)3。99.85% Al(NO 3 ) 3 .9H 2 O and 0.15% additives are used as raw materials, and the raw material components and weight percentage content of the 0.15% additive are 30% nano-SiO 2 , 5% Y(NO 3 ) 3 , 10% Fe(NO 3 ) 3 , 26% Ca(NO 3 ) 2 , 14% Mg(NO 3 ) 2 and 15% Cr(NO 3 ) 3 .
首先将Al(NO3)3·9H2O溶于水后过滤去除杂质,配成0.1mol/L的含Al3+的水溶液;First, dissolve Al(NO 3 ) 3 9H 2 O in water, filter to remove impurities, and prepare a 0.1mol/L aqueous solution containing Al 3+ ;
向上述溶液中滴加沉淀剂氨水并搅拌使含该Al3+的水溶液完全凝胶化,再经抽滤、洗涤得Al(OH)3凝胶;In above-mentioned solution, add precipitating agent ammoniacal liquor dropwise and stir to make the aqueous solution containing this Al 3+ fully gel, then through suction filtration, washing obtain Al(OH) 3 gel;
将0.15%添加剂加入到Al(OH)3胶体中混匀;将含有添加剂的Al(OH)3胶体干燥,得的Al(OH)3固体,再造粒并进行筛分和分级;Add 0.15% additives to Al(OH) 3 colloids and mix well; dry the Al(OH) 3 colloids containing additives to obtain Al(OH) 3 solids, regranulate and sieve and classify;
将已预筛分和分级的Al(OH)3在1400℃下煅烧,再进一步的过筛、分级,制得不同粒度的板状纳米晶刚玉磨料。The pre-screened and classified Al(OH) 3 is calcined at 1400°C, and then further screened and classified to obtain plate-shaped nanocrystalline corundum abrasives with different particle sizes.
刚玉磨料内部显微晶粒尺寸大小为1.23μm,韧性为3.18±0.12MPa·m1/2。The microscopic grain size inside the corundum abrasive is 1.23μm, and the toughness is 3.18±0.12MPa·m 1/2 .
实施例2Example 2
采用99.5%的Al2(SO4)3·18H2O和0.5%的添加剂为原料,所述0.5%添加剂的原料组分及重量百分比含量为10%纳米SiO2、30%Fe(NO3)3、18%Y(NO3)3、15%Ca(NO3)2和27%Mg(NO3)2。99.5% Al 2 (SO 4 ) 3 ·18H 2 O and 0.5% additives are used as raw materials, and the raw material components and weight percentage content of the 0.5% additive are 10% nano-SiO 2 , 30% Fe(NO 3 ) 3. 18% Y(NO 3 ) 3 , 15% Ca(NO 3 ) 2 and 27% Mg(NO 3 ) 2 .
首先将Al(NO3)3·9H2O溶于水后过滤去除杂质,配成0.2mol/L的含Al3+的水溶液;First, dissolve Al(NO 3 ) 3 9H 2 O in water, filter to remove impurities, and prepare a 0.2mol/L aqueous solution containing Al 3+ ;
向上述溶液中滴加沉淀剂氨水并搅拌使含该Al3+的水溶液完全凝胶化,再经抽滤、洗涤得Al(OH)3凝胶;In above-mentioned solution, add precipitating agent ammoniacal liquor dropwise and stir to make the aqueous solution containing this Al 3+ fully gel, then through suction filtration, washing obtain Al(OH) 3 gel;
将0.5%添加剂剂加入到Al(OH)3胶体中混匀。将含有添加剂的Al(OH)3胶体干燥所得的Al(OH)3固体,再造粒并进行筛分和分级;Add 0.5% additive to the Al(OH) 3 colloid and mix well. Al(OH) solid obtained by drying the Al(OH) colloid containing the additive, regranulating and sieving and classifying;
将已预筛分和分级的Al(OH)3在1150℃下煅烧,再进一步的过筛、分级,制得不同粒度的板状纳米晶刚玉磨料。The pre-screened and classified Al(OH) 3 is calcined at 1150°C, and then further screened and classified to obtain plate-shaped nanocrystalline corundum abrasives with different particle sizes.
刚玉磨料内部显微晶粒尺寸大小为60nm,韧性为3.41±0.06MPa·m1/2。The microscopic grain size inside the corundum abrasive is 60nm, and the toughness is 3.41±0.06MPa·m 1/2 .
实施例3Example 3
采用99.3%的Al(NO3)3·9H2O和0.7%的添加剂为原料,所述0.7%添加剂的原料组分及重量百分比含量为9%Fe(NO3)3、21%Ca(NO3)2、45%Mg(NO3)2和25%Cr(NO3)3。Using 99.3% Al(NO 3 ) 3 ·9H 2 O and 0.7% additives as raw materials, the raw material components and weight percentage content of the 0.7% additives are 9% Fe(NO 3 ) 3 , 21% Ca(NO 3 ) 2 , 45% Mg(NO 3 ) 2 and 25% Cr(NO 3 ) 3 .
首先将Al(NO3)3·9H2O溶于水后过滤去除杂质,配成0.4mol/L的含Al3+的水溶液;First, dissolve Al(NO 3 ) 3 9H 2 O in water, filter to remove impurities, and prepare a 0.4mol/L aqueous solution containing Al 3+ ;
向上述溶液中滴加沉淀剂氨水并搅拌使含该Al3+的水溶液完全凝胶化,再经抽滤、洗涤得Al(OH)3凝胶;In above-mentioned solution, add precipitating agent ammoniacal liquor dropwise and stir to make the aqueous solution containing this Al 3+ fully gel, then through suction filtration, washing obtain Al(OH) 3 gel;
将0.7%添加剂剂加入到Al(OH)3胶体中混匀。Add 0.7% additive to the Al(OH) 3 colloid and mix well.
将含有添加剂的Al(OH)3胶体干燥所得的Al(OH)3固体,再造粒并进行筛分和分级;Al(OH) solid obtained by drying the Al(OH) colloid containing the additive, regranulating and sieving and classifying;
将已预筛分和分级的Al(OH)3在1310℃下煅烧,再进一步的过筛、分级,制得不同粒度的板状纳米晶刚玉磨料。The pre-screened and classified Al(OH) 3 is calcined at 1310°C, and then further screened and classified to obtain plate-shaped nanocrystalline corundum abrasives with different particle sizes.
刚玉磨料内部显微晶粒尺寸大小为560nm,韧性为3.27±0.10MPa·m1/2。The microscopic grain size inside the corundum abrasive is 560nm, and the toughness is 3.27±0.10MPa·m 1/2 .
实施例4Example 4
采用99.15%的Al(NO3)3·9H2O和0.85%的添加剂为原料,所述0.85%添加剂为100%Ca(NO3)2。99.15% Al(NO 3 ) 3 ·9H 2 O and 0.85% additive are used as raw materials, and the 0.85% additive is 100% Ca(NO 3 ) 2 .
首先将Al2(SO4)3·18H2O溶于水后过滤去除杂质,配成0.6mol/L的含Al3+的水溶液;First, dissolve Al 2 (SO 4 ) 3 ·18H 2 O in water, filter to remove impurities, and prepare a 0.6mol/L aqueous solution containing Al 3+ ;
向上述溶液中滴加沉淀剂氨水并搅拌使含该Al3+的水溶液完全凝胶化,再经抽滤、洗涤得Al(OH)3凝胶;In above-mentioned solution, add precipitating agent ammoniacal liquor dropwise and stir to make the aqueous solution containing this Al 3+ fully gel, then through suction filtration, washing obtain Al(OH) 3 gel;
将0.85%添加剂加入到Al(OH)3胶体中混匀;Add 0.85% additive to the Al(OH) 3 colloid and mix well;
将含有添加剂的Al(OH)3胶体干燥所得的Al(OH)3固体,再造粒并进行筛分和分级;Al(OH) solid obtained by drying the Al(OH) colloid containing the additive, regranulating and sieving and classifying;
将已预筛分和分级的Al(OH)3在1220℃下煅烧,再进一步的过筛、分级,制得不同粒度的板状纳米晶刚玉磨料;Calcinate the pre-screened and classified Al(OH) 3 at 1220°C, and then further screen and classify to obtain plate-shaped nanocrystalline corundum abrasives with different particle sizes;
刚玉磨料内部显微晶粒尺寸大小为120nm,韧性为3.36±0.08MPa·m1/2。The microscopic grain size inside the corundum abrasive is 120nm, and the toughness is 3.36±0.08MPa·m 1/2 .
现有技术下刚玉磨料的显微晶粒尺寸一般为0.2~5μm,韧性为2.75~2.91MPa·m1/2,而本发明刚玉磨料的显微晶粒尺寸为40nm~2μm,韧性为3.18~3.45MPa·m1/2,降低了刚玉磨料内部显微晶粒尺寸,并且提高刚玉磨料韧性9~25%。The microscopic grain size of the corundum abrasive in the prior art is generally 0.2-5 μm, and the toughness is 2.75-2.91 MPa·m 1/2 , while the microscopic grain size of the corundum abrasive of the present invention is 40 nm-2 μm, and the toughness is 3.18-2 μm. 3.45MPa·m 1/2 , which reduces the microscopic grain size inside the corundum abrasive and increases the toughness of the corundum abrasive by 9-25%.
本发明并不局限于上述实施例,很多细节的变化是可能的,但这并不因此违背本发明的范围和精神。The present invention is not limited to the above-described embodiments, and changes in many details are possible without departing from the scope and spirit of the present invention.
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2011103687962A CN102492394A (en) | 2011-11-18 | 2011-11-18 | Preparation method of hexagonal tabular nano-crystal corundum abrasive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2011103687962A CN102492394A (en) | 2011-11-18 | 2011-11-18 | Preparation method of hexagonal tabular nano-crystal corundum abrasive |
Publications (1)
Publication Number | Publication Date |
---|---|
CN102492394A true CN102492394A (en) | 2012-06-13 |
Family
ID=46184258
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2011103687962A Pending CN102492394A (en) | 2011-11-18 | 2011-11-18 | Preparation method of hexagonal tabular nano-crystal corundum abrasive |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN102492394A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102732214A (en) * | 2012-06-20 | 2012-10-17 | 天津大学 | Ceramic corundum abrasive containing multiphase additive |
CN103242033A (en) * | 2013-04-27 | 2013-08-14 | 天津大学 | Ceramic corundum grinding material and preparation method thereof |
CN105586005A (en) * | 2016-01-14 | 2016-05-18 | 洛阳三睿宝纳米科技有限公司 | Nano corundum abrasive and preparation method thereof |
CN105645933A (en) * | 2016-01-18 | 2016-06-08 | 天津大学 | Sheet-structure ceramic corundum abrasive material and preparation method thereof |
CN106083001A (en) * | 2016-06-17 | 2016-11-09 | 天津大学 | Nanocrystalline blue ceramic corundum abrasive and preparation method thereof |
CN108531133A (en) * | 2018-06-05 | 2018-09-14 | 遵义市播州区铁厂创业刚玉有限责任公司 | A kind of preparation method of the nanocrystalline corundum abrasive of six square plates shape |
CN109592971A (en) * | 2017-09-30 | 2019-04-09 | 天津大学 | A kind of fused alumina zirconia abrasive material and preparation method thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101434829A (en) * | 2008-12-19 | 2009-05-20 | 天津大学 | Novel corundum abrasive and preparation thereof |
-
2011
- 2011-11-18 CN CN2011103687962A patent/CN102492394A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101434829A (en) * | 2008-12-19 | 2009-05-20 | 天津大学 | Novel corundum abrasive and preparation thereof |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102732214A (en) * | 2012-06-20 | 2012-10-17 | 天津大学 | Ceramic corundum abrasive containing multiphase additive |
CN102732214B (en) * | 2012-06-20 | 2014-04-02 | 天津大学 | Ceramic corundum abrasive containing multiphase additive |
CN103242033A (en) * | 2013-04-27 | 2013-08-14 | 天津大学 | Ceramic corundum grinding material and preparation method thereof |
CN105586005A (en) * | 2016-01-14 | 2016-05-18 | 洛阳三睿宝纳米科技有限公司 | Nano corundum abrasive and preparation method thereof |
CN105586005B (en) * | 2016-01-14 | 2018-02-23 | 洛阳三睿宝纳米科技有限公司 | A kind of preparation method of Nano Alumina Abrasive |
CN105645933A (en) * | 2016-01-18 | 2016-06-08 | 天津大学 | Sheet-structure ceramic corundum abrasive material and preparation method thereof |
CN105645933B (en) * | 2016-01-18 | 2018-08-03 | 天津大学 | A kind of laminated structure Ceramic corundum abrasive and preparation method thereof |
CN106083001A (en) * | 2016-06-17 | 2016-11-09 | 天津大学 | Nanocrystalline blue ceramic corundum abrasive and preparation method thereof |
CN106083001B (en) * | 2016-06-17 | 2019-07-23 | 天津大学 | Nanocrystalline blue ceramic corundum abrasive and preparation method thereof |
CN109592971A (en) * | 2017-09-30 | 2019-04-09 | 天津大学 | A kind of fused alumina zirconia abrasive material and preparation method thereof |
CN108531133A (en) * | 2018-06-05 | 2018-09-14 | 遵义市播州区铁厂创业刚玉有限责任公司 | A kind of preparation method of the nanocrystalline corundum abrasive of six square plates shape |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102492394A (en) | Preparation method of hexagonal tabular nano-crystal corundum abrasive | |
TWI461364B (en) | Method for producing boehmite particles and method for producing aluminum particles | |
JP5647359B2 (en) | Method for preparing α-alumina abrasive | |
CN105645933B (en) | A kind of laminated structure Ceramic corundum abrasive and preparation method thereof | |
CN104556176B (en) | A kind of preparation method of aluminum oxide nanoparticle | |
CN105858706B (en) | The preparation method of yttrium oxide powder | |
CN101921575B (en) | Manufacturing method of cubic boron nitride-aluminum oxide polycrystal compounded abrasive | |
CN102732214B (en) | Ceramic corundum abrasive containing multiphase additive | |
TW201946873A (en) | Alumina particle | |
CN108772569A (en) | A kind of hydrothermal preparation method of ultrafine nano tungsten powder | |
CN106966705A (en) | A kind of nanocrystalline ceramics corundum abrasive containing complex phase additive | |
CN103570049B (en) | Method for preparing completely dispersed alpha aluminum oxide nano particles | |
CN115893461B (en) | Production process of nano alumina polishing powder | |
CN103373845B (en) | Indium Gallium Zinc Oxide and Its Preparation and Application | |
CN107406268A (en) | The production method of nanometer Alpha's aluminum oxide | |
JP2013104023A (en) | Zirconia abrasive and method for manufacturing the same | |
CN105586005B (en) | A kind of preparation method of Nano Alumina Abrasive | |
CN104585238B (en) | Supersonic and co-deposition and ultrasonic molten-salt growth method prepare Ag2MoO4‑CuMoO4Compound antibacterial powder | |
CN102775135A (en) | Novel ceramic corundum abrasive | |
CN115805305A (en) | Spherical composite powder and preparation method thereof | |
CN118359222A (en) | Cerium oxide flake powder containing nano crystals and preparation method thereof | |
CN104176759A (en) | A Molten Salt Method for Preparing Cubic CeO2 Nanomaterials | |
CN105397102B (en) | A kind of preparation method of aluminum oxide coated tungsten powder | |
CN108531133A (en) | A kind of preparation method of the nanocrystalline corundum abrasive of six square plates shape | |
CN107311219B (en) | The purification method of azurite pigment |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20120613 |