CN1360091A - Process for synthesizing yellow cubic borium nitride monocrystal with Mg as catalyst - Google Patents
Process for synthesizing yellow cubic borium nitride monocrystal with Mg as catalyst Download PDFInfo
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- CN1360091A CN1360091A CN 01138743 CN01138743A CN1360091A CN 1360091 A CN1360091 A CN 1360091A CN 01138743 CN01138743 CN 01138743 CN 01138743 A CN01138743 A CN 01138743A CN 1360091 A CN1360091 A CN 1360091A
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Abstract
A process for synthesizing yellow cubic boron nitride monocrystal using hexagonal boron nitride as raw material, metallic Mg as catalyst, and magnesium (or calcium) oxide as additive incldues mixing, charging in graphite container, and pressing at 1000-2000 deg.C and 4-6 GPa for 4-10 min. Its advantages are high stability, low cost, and simple process.
Description
Technical field
The invention belongs to a kind of synthetic method of superhard material, the method for the translucent cubic boron nitride monocrystal of particularly a kind of synthesizing yellow.
Background technology
With hexagonal boron nitride is raw material, is catalyst synthesizing cubic boron nitride monocrystalline with MAGNESIUM METAL, is a kind of widely used method.But the single-crystal fault that synthesizes is many, hardness is low, black non transparent.The prior art the most close with the present invention is that metal nitrides such as employing lithium, calcium are the method for the synthetic light cubic boron nitride monocrystal of catalyst.It is special to see Japanese Patent JP56-140013[for details, day]/-1981.11.2-55-40451 (1980.3.31); Int.Cl.ColB21/064, Bolj27/24.The major technique content comprises, is raw material with hexagonal boron nitride, uses lithium nitride, and CaCl2 is a catalyst, through batch mixing-pressure injection shaping-assembling-High Temperature High Pressure synthetic technological process, synthesizes light cubic boron nitride monocrystal.Before batch mixing, prepare lithium nitride, CaCl2 catalyst, promptly under nitrogen atmosphere, prepare lithium nitride, CaCl2 through high-temperature ammonolysis with metallic lithium, calcium metal.Because metallic lithium, calcium metal all are active metallic elements, preserve and make its synthesizing nitride that suitable difficulty all be arranged, make the technology of the synthetic light cubic boron nitride monocrystal quite trouble that becomes, because metallic lithium, calcium metal are more valuable, so the cost of synthesizing cubic boron nitride monocrystalline is very high.
Summary of the invention
Cubic boron nitride is a kind of pure synthetic material.Its hardness is only second to diamond, is the good superhard material of processing iron family element ting and alloy.Synthetic color is more shallow, and the less cubic boron nitride monocrystal of defective is always necessary with the requirement that adapts to processing industry.The present invention adopts cheap MAGNESIUM METAL to make catalyst, adopt cheap magnesium oxide or calcium oxide to make additive, the translucent cubic boron nitride monocrystal of synthesizing yellow, can overcome use in the synthetic light cubic boron nitride crystal process of background technology nitride, boron nitride as catalyst bring complicacy, simplify technological process, reduce production costs.Also the someone studies Magnesium peroxide cubic boron nitride monocrystalline synthetic influence, thinks that magnesium oxide is unfavorable to the synthesis of cubic boron nitride crystal, sees that specifically people such as H.Lofenz is published in J.Mater.Sci.Lett, and 7 (1988) 23, exercise question is that " MgO is to using Mg
3N
2Do the influence of the synthetic cBN of catalyst " article.Off the beaten track technology of the present invention and conventional understanding are used MAGNESIUM METAL to add magnesium oxide, calcium oxide as catalyst or are made MAGNESIUM METAL oxidation in synthetic, and use and the essentially identical technological process of background technology are produced the yellow transparent cubic boron nitride monocrystal.
Specific embodiment of the present invention is as described below.
With hexagonal boron nitride (hBN) is raw material, is catalyst with MAGNESIUM METAL (Mg), is additive with magnesium oxide (MgO) or calcium oxide (CaO), through batch mixing-pressure injection crystal vessel that is shaped-packs into, becomes assembly block; Assembly block is put into the cavity of press, through High Temperature High Pressure synthesizing yellow cubic boron nitride (cBN) monocrystalline.HBN, Mg, MgO or CaO are 1 by mass ratio in the batch mixing: (0.1～0.3): (0.3～1); High Temperature High Pressure synthetic condition is 1000～2000 ℃ in temperature promptly for synthetic cBN normal condition, and pressure is to be incubated 4～10 minutes under 4.0～6.0Gpa condition.
Aforesaid assembly block can be assembled by mode of loading in mixture or layer dress mode.Said loading in mixture is that hBN, Mg, MgO or CaO are pressed into column behind the uniform mixing in proportion, reinstalls crystal vessel.Said layer dress is to be pressed into sheet after hBN, Mg are mixed, and MgO or CaO also are pressed into sheet, the crystal vessel of again these two kinds of sheets alternately being packed into.Columnar material here or flaky material diameter should match with the intracavity diameter of crystal vessel; Alternately pack into the height of crystal vessel of the height of post or two kinds of sheets should match with the inner chamber height of crystal vessel.
Can magnesium oxide or calcium oxide account for the scale of raw material among the present invention, be the key that synthesize the glassy yellow cubic boron nitride crystal of color even.
The present invention is owing to make catalyst and additive with Mg, MgO, CaO, and stable being easy to of its raw material taken care of, than using Li
3N, Ca
3N
2Want much cheap; The process of producing Mg, MgO, CaO is also much easier, be of value to the synthetic of cBN monocrystalline, promptly overcome the inconvenience that complicacy, oxidisability and the use of using nitride to bring as catalyst are preserved, simplified technological process, reduced production cost, be more convenient for implementing.The present invention is owing to add MgO, the CaO of appropriate ratio, and products obtained therefrom is yellow translucent cBN crystal, has broken the technology prejudice that synthetic cBN crystal can not use MgO.
Embodiment
Embodiment 1: make additive with the MgO powder, adopt the mode that loads in mixture
This compound experiment in finish on the homemade DS029B swaging machine.With hexagonal boron nitride, magnesium powder in 85: 15 ratio uniform mixing of quality after, add the magnesia powder that accounts for preceding two kinds of material total masses 25～30% again, be pressed into column behind the mixing, put into the heating crystal vessel, at 4.0-6.0GPa pressure, insulation is 5 minutes under the 1000-2000 ℃ of condition, stop heat back release, obtain the yellow transparent cubic boron nitride crystal of color even after sour alkali is handled, crystal growth is good, structural integrity, energy spectrum analysis show that boron nitrogen ratio was near 1: 1.
Embodiment 2: make additive with the MgO piece, adopt the mode that loads in mixture
Experiment is carried out on the high-tension apparatus identical with embodiment 1, and processing condition are with embodiment 1 when synthetic.Raw material is configured to: with hexagonal boron nitride and metal magnesium powder in 85: 15 ratio uniform mixing of quality, mix with the magnesia block that accounts for preceding two kinds of material total mass 30～40% ratios again, being pressed into column according to the size of synthetic cavity then packs in the heating crystal vessel, synthetic under high-temperature and high-pressure conditions, the gained cubic boron nitride crystal is translucent yellow, crystal growth is good, structural integrity, and energy spectrum analysis shows that boron nitrogen ratio was near 1: 1.
Embodiment 3: make additive with the MgO powder, adopt layer dress mode
In 80: 20 ratio of quality with hexagonal boron nitride and metal magnesium powder uniform mixing, size according to synthetic cavity is pressed into thick about 1 millimeter sheet, again magnesia powder is pressed into hexagonal boron nitride, the metal magnesium powder material piece is onesize and the sheet of thickness, above-mentioned two kinds of sheets that press are alternately packed in the heating crystal vessel into synthetic cBN under high-temperature and high-pressure conditions.Gained cBN crystal is translucent yellow, and crystal growth is good, structural integrity, and energy spectrum analysis shows that boron nitrogen ratio was near 1: 1.
Embodiment 4: make additive with the CaO powder
Identical with the technological process of embodiment 1 and embodiment 3, just replace the MgO powder to make additive with the CaO powder, effect is also basic identical with embodiment 1, embodiment 3.
Claims (2)
1, a kind ofly making the method for catalyst synthesizing yellow cubic boron nitride monocrystal with MAGNESIUM METAL, is raw material with the hexagonal boron nitride, through batch mixing-pressure injection crystal vessel that is shaped-packs into, becomes assembly block; Assembly block is put into the cavity of press, in temperature is that 1000～2000 ℃, pressure are to be incubated 4～10 minutes synthesizing yellow cubic boron nitride monocrystals under 4.0～6.0Gpa condition, it is characterized in that, with the MAGNESIUM METAL is catalyst, with magnesium oxide or calcium oxide is that additive carries out batch mixing, and hexagonal boron nitride, MAGNESIUM METAL, magnesium oxide or calcium oxide are 1 in the ratio of quality: (0.1～0.3): (0.3～1).
2, according to the described method of making catalyst synthesizing yellow cubic boron nitride monocrystal with MAGNESIUM METAL of claim 1, it is characterized in that, said assembly block can be assembled by mode of loading in mixture or layer dress mode, said loading in mixture, be that hexagonal boron nitride, MAGNESIUM METAL, magnesium oxide or calcium oxide are pressed into column behind the uniform mixing in proportion, reinstall crystal vessel; Said layer dress is to be pressed into sheet after hexagonal boron nitride, MAGNESIUM METAL are mixed, and magnesium oxide or calcium oxide also are pressed into sheet, the crystal vessel of again these two kinds of sheets alternately being packed into.
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| Application Number | Priority Date | Filing Date | Title |
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| CNB011387432A CN1137294C (en) | 2001-11-29 | 2001-11-29 | Process for synthesizing yellow cubic borium nitride monocrystal with Mg as catalyst |
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| CNB011387432A CN1137294C (en) | 2001-11-29 | 2001-11-29 | Process for synthesizing yellow cubic borium nitride monocrystal with Mg as catalyst |
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| CN1360091A true CN1360091A (en) | 2002-07-24 |
| CN1137294C CN1137294C (en) | 2004-02-04 |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103272529A (en) * | 2013-05-28 | 2013-09-04 | 柳州市大荣非金属材料有限公司 | Method for synthesizing cubic boron nitride polycrystalline particles |
| CN103924288A (en) * | 2014-04-01 | 2014-07-16 | 许斌 | Method for preparing cubic boron nitride monocrystal micro powder by using magnesium-based compound catalyst and application of cubic boron nitride monocrystal micro powder |
| CN105386118A (en) * | 2014-08-26 | 2016-03-09 | 信阳市德隆超硬材料有限公司 | Method for synthesizing coarse particle size cubic boron nitride single crystal through magnesium-based catalyst |
| CN107523875A (en) * | 2017-10-12 | 2017-12-29 | 信阳市德隆超硬材料有限公司 | A kind of cubic boron nitride monocrystal and preparation method thereof |
| CN108144554A (en) * | 2017-12-04 | 2018-06-12 | 郑州中南杰特超硬材料有限公司 | A kind of manufacture craft of novel diamond synthesis column |
| CN109825880A (en) * | 2019-03-07 | 2019-05-31 | 信阳市德隆超硬材料有限公司 | A kind of cubic boron nitride monocrystal and preparation method thereof |
-
2001
- 2001-11-29 CN CNB011387432A patent/CN1137294C/en not_active Expired - Fee Related
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103272529A (en) * | 2013-05-28 | 2013-09-04 | 柳州市大荣非金属材料有限公司 | Method for synthesizing cubic boron nitride polycrystalline particles |
| CN103924288A (en) * | 2014-04-01 | 2014-07-16 | 许斌 | Method for preparing cubic boron nitride monocrystal micro powder by using magnesium-based compound catalyst and application of cubic boron nitride monocrystal micro powder |
| CN103924288B (en) * | 2014-04-01 | 2016-08-17 | 山东建筑大学 | Use the cubic boron nitride monocrystal micropowder preparation method and application of magnesio composite catalyst |
| CN105386118A (en) * | 2014-08-26 | 2016-03-09 | 信阳市德隆超硬材料有限公司 | Method for synthesizing coarse particle size cubic boron nitride single crystal through magnesium-based catalyst |
| CN107523875A (en) * | 2017-10-12 | 2017-12-29 | 信阳市德隆超硬材料有限公司 | A kind of cubic boron nitride monocrystal and preparation method thereof |
| CN108144554A (en) * | 2017-12-04 | 2018-06-12 | 郑州中南杰特超硬材料有限公司 | A kind of manufacture craft of novel diamond synthesis column |
| CN109825880A (en) * | 2019-03-07 | 2019-05-31 | 信阳市德隆超硬材料有限公司 | A kind of cubic boron nitride monocrystal and preparation method thereof |
| CN109825880B (en) * | 2019-03-07 | 2021-08-24 | 信阳市德隆超硬材料有限公司 | Cubic boron nitride single crystal and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN1137294C (en) | 2004-02-04 |
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