JPS6081009A - Manufacture of cubic-crystal boron nitride compound - Google Patents
Manufacture of cubic-crystal boron nitride compoundInfo
- Publication number
- JPS6081009A JPS6081009A JP18758283A JP18758283A JPS6081009A JP S6081009 A JPS6081009 A JP S6081009A JP 18758283 A JP18758283 A JP 18758283A JP 18758283 A JP18758283 A JP 18758283A JP S6081009 A JPS6081009 A JP S6081009A
- Authority
- JP
- Japan
- Prior art keywords
- boron nitride
- cubic
- nitride compound
- formula
- boroamino
- 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
Landscapes
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
Description
【発明の詳細な説明】
この発明は立方晶窒化硼素化合物の製造方法に関するも
のである。立方晶窒化硼素化合物は切削、研削等の工具
材として注目されているものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing cubic boron nitride compounds. Cubic boron nitride compounds are attracting attention as tool materials for cutting, grinding, etc.
従来、か\る立方晶窒化硼素化合物は、六方晶型窒化硼
素化合物を高温高圧下で処理することによって得られて
いた。あるいはまた、触媒を使って処理する触媒法によ
って造られていた。Conventionally, such cubic boron nitride compounds have been obtained by treating hexagonal boron nitride compounds at high temperatures and high pressures. Alternatively, it was produced by a catalytic process using a catalyst.
しかしながらこれらの方法においては、高温高圧を要す
るものは、容器装置が犬がかりとならざるを得す経済性
からみても工業的な方法とけいえない。触媒を使用する
ものは、立方晶型単結晶窒化硼素が得難かったり、得ら
れても7ヤープな稜部を持っていなかったりするので、
切削性及び研削性の点で劣る等の欠点をもっている。However, in these methods, those requiring high temperature and high pressure cannot be called industrial methods even from an economic point of view, as the container equipment must be dependent on the equipment. In those that use a catalyst, it is difficult to obtain cubic single crystal boron nitride, or even if it is obtained, it does not have a 7-year edge.
It has disadvantages such as poor cutting and grinding properties.
この発明は、常圧下で、ポロアミノポリマーH+B H
−NH−)n Hを加熱することによって立方晶型窒化
硼素を造ることができるという知見を得、これにもとづ
いてなされたものである。This invention provides polyamino polymer H+B H under normal pressure.
The present invention was based on the finding that cubic boron nitride can be produced by heating -NH-)nH.
即ち式 H−(−BH−NH−)n Hで示されるポロ
アミノポリマーをその1\で゛、あるいは適宜溶媒に溶
解したものを基質の表面に塗布したのち、加熱すること
によって極めて容易に立方晶型窒化硼素を得ることがで
きる。、ここにおいて用いられるポロアミノポリマーは
次のようにして造られる。即ち、水素化アルカリ金属ボ
ラン例えばニウムなどをエヂルエーテル中絶体温度77
°にで反応させたのち、反応混合物の温度を室温にまで
上昇させることによって、生成物ポロアミノモノマーが
重合してポロアミノポリマーが生成する。That is, a polyamino polymer represented by the formula H-(-BH-NH-)nH is applied to the surface of a substrate in its 1\ form, or dissolved in an appropriate solvent, and then heated to form cubes very easily. Crystalline boron nitride can be obtained. , the polyamino polymer used herein is made as follows. That is, a hydrogenated alkali metal borane, such as nium, is heated to an ether temperature of 77.
After reacting at 30°C, the product polyamino monomer polymerizes to form a polyamino polymer by increasing the temperature of the reaction mixture to room temperature.
加熱は少くとも1700以上の温度を必要とじ2000
以上の方が、生成した窒化硼素が完全に立方晶型に変っ
ている点からみて好適である。溶媒に溶かして、塗布す
る場合の溶媒としては、ジメチルホルムアミド、ジメチ
ルアセタミド、ジメチルスルホキシド、HMPAなどが
あげられ、被塗布基質としては、酸化アルミニュ以下実
施例を記述して、本発明を更に詳しく説明する。Heating requires a temperature of at least 1700°C or higher and 2000°C.
The above method is preferable in that the generated boron nitride is completely transformed into a cubic crystal type. When applied by dissolving in a solvent, examples of the solvent include dimethylformamide, dimethylacetamide, dimethyl sulfoxide, HMPA, etc., and examples of the substrate to be applied include aluminum oxide. explain in detail.
実施例1
ポロアミノポリマー10flを、ジメチルホルムアミド
7pomlに溶かし、これをα−酸化アルミニウムの表
面に3回繰り返し塗布した。Example 1 10 fl of a polyamino polymer was dissolved in 7 poml of dimethylformamide, and this was repeatedly applied to the surface of α-aluminum oxide three times.
風乾したのち200CVC2時間加熱した。After air drying, it was heated at 200 CVC for 2 hours.
α−酸化アルミニウムの表面に白色の固体が生成してい
るのを認めた。このものは、X−線回折により立方晶窒
化硼素であることが認められた。It was observed that a white solid was formed on the surface of α-aluminum oxide. This material was confirmed to be cubic boron nitride by X-ray diffraction.
粒子径0.1〜1だ。The particle size is 0.1-1.
X−線回折データー
2θ d
1.45.1° 2.09
2、74.0° 1,28
8、90.0° 1.09
参考例
本発明で使用されるポロアミノポリマーは次のようにし
て合成された。X-ray diffraction data 2θ d 1.45.1° 2.09 2, 74.0° 1,28 8, 90.0° 1.09 Reference Example The polyamino polymer used in the present invention was prepared as follows. was synthesized.
水素化硼素リチュム220g、塩化アンモニウム540
gをエチルエーテル2000m1に加え77°にの温度
で反応させた。水素の発生が止んだ時、反応が終了した
。次いで、反応混合物を室温にまで昇温させると、水素
ガスを発生しポロアミンポリマーが生成した。Boron hydride lithium 220g, ammonium chloride 540g
g was added to 2000 ml of ethyl ether and reacted at a temperature of 77°. The reaction was complete when hydrogen evolution ceased. The reaction mixture was then heated to room temperature, generating hydrogen gas and forming a polyamine polymer.
得られた反応混合物から、水洗によって塩化リチウムを
除き、ポロアミノポリマーを得た。Lithium chloride was removed from the resulting reaction mixture by washing with water to obtain a polyamino polymer.
収率95%Yield 95%
Claims (1)
温度に加熱し、立方晶窒化硼素化合物を得ることを特徴
とする立方晶窒化硼素化合物の製造方法 〔式中nは3以上の整数を示す〕[Claims] A method for producing a cubic boron nitride compound, which comprises heating a polyamino polymer represented by the formula % to a temperature of 170° C. or higher under normal pressure to obtain a cubic boron nitride compound. [In the formula, n represents an integer of 3 or more]
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18758283A JPS6081009A (en) | 1983-10-05 | 1983-10-05 | Manufacture of cubic-crystal boron nitride compound |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18758283A JPS6081009A (en) | 1983-10-05 | 1983-10-05 | Manufacture of cubic-crystal boron nitride compound |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6081009A true JPS6081009A (en) | 1985-05-09 |
Family
ID=16208625
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18758283A Pending JPS6081009A (en) | 1983-10-05 | 1983-10-05 | Manufacture of cubic-crystal boron nitride compound |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6081009A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02254168A (en) * | 1989-03-27 | 1990-10-12 | Yukio Ichinose | Production of boron nitride |
-
1983
- 1983-10-05 JP JP18758283A patent/JPS6081009A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02254168A (en) * | 1989-03-27 | 1990-10-12 | Yukio Ichinose | Production of boron nitride |
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