JPH0931445A - Grinding grain - Google Patents
Grinding grainInfo
- Publication number
- JPH0931445A JPH0931445A JP18897795A JP18897795A JPH0931445A JP H0931445 A JPH0931445 A JP H0931445A JP 18897795 A JP18897795 A JP 18897795A JP 18897795 A JP18897795 A JP 18897795A JP H0931445 A JPH0931445 A JP H0931445A
- Authority
- JP
- Japan
- Prior art keywords
- grinding
- abrasive grains
- boron nitride
- cubic
- cbn abrasive
- 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
- 238000000227 grinding Methods 0.000 title abstract description 70
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000001301 oxygen Substances 0.000 claims abstract description 23
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 23
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910052582 BN Inorganic materials 0.000 claims abstract description 11
- 239000006061 abrasive grain Substances 0.000 claims description 94
- 239000013078 crystal Substances 0.000 claims description 34
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 238000005299 abrasion Methods 0.000 abstract description 6
- 239000002994 raw material Substances 0.000 abstract description 5
- 239000004575 stone Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 description 8
- 238000005520 cutting process Methods 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000003776 cleavage reaction Methods 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 230000007017 scission Effects 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 229910003460 diamond Inorganic materials 0.000 description 3
- 239000010432 diamond Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229910001315 Tool steel Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000012916 structural analysis Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
Landscapes
- Polishing Bodies And Polishing Tools (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は研削砥石用の砥粒に
関するものである。本発明の砥粒が応用される研削砥石
としては、特に鉄系金属加工用の重研削、高速研削用の
メタルボンド砥石、電着砥石、ビトリファイド砥石等が
あげられる。TECHNICAL FIELD The present invention relates to abrasive grains for a grinding wheel. Examples of grinding wheels to which the abrasive grains of the present invention are applied include heavy grinding for iron-based metal processing, metal bond grinding wheels for high-speed grinding, electrodeposition grinding wheels, and vitrified grinding wheels.
【0002】[0002]
【従来の技術】窒化ほう素の高圧相である立方晶窒化ほ
う素(cBN)はダイヤモンドに次ぐ硬さと熱伝導率を
有し、鉄系金属と反応しないとうダイヤモンドにはない
特徴を持つことから鉄系金属の研削加工用砥粒としての
利用が進められている。2. Description of the Prior Art Cubic boron nitride (cBN), which is a high-pressure phase of boron nitride, has hardness and thermal conductivity second only to diamond, and has characteristics that diamond does not have if it does not react with iron-based metals. Utilization of iron-based metals as abrasive grains for grinding is being promoted.
【0003】近年の研削加工は、省力化、無人化の方向
にある。その具体例は、重研削、高速研削であるが、こ
のような過酷な研削条件下では砥石の切れ味が悪いと研
削抵抗が大きくなり、工作機械へ大きな負荷がかかる。
このため、工作機械の高剛性化や高能力化が実施されて
いるが省力化の面から好ましくなく、切れ味が良く研削
抵抗を安定して小さく、しかも耐摩耗性に優れた砥石が
待ち望まれている。[0003] In recent years, grinding has been directed toward labor saving and unmanned operation. Specific examples thereof are heavy grinding and high speed grinding, but under such severe grinding conditions, if the sharpness of the grindstone is poor, the grinding resistance increases and a heavy load is applied to the machine tool.
For this reason, machine tools have been made to have higher rigidity and higher performance, but this is not preferable from the viewpoint of labor saving, and a grindstone with good sharpness, stable and small grinding resistance, and excellent wear resistance is desired. There is.
【0004】一般にcBN砥石の研削抵抗は、「cBN
ホイール研削加工技術」(1988年 工業調査会発
行)でも紹介されているように砥石の使用初期に著しく
高いことが知られている。Generally, the grinding resistance of a cBN grindstone is "cBN
It is known that it is extremely high in the early stages of use of the grinding wheel, as also introduced in "Wheel grinding technology" (published by the Industrial Research Board in 1988).
【0005】cBN砥石に用いられるcBN砥粒を大別
すると、多結晶型と単結晶型の2種類のものがある。多
結晶型cBN砥粒は、微細なcBN結晶粒子が互いに強
固に結合した多結晶体構造を有するため、粒子一つが単
結晶により構成される単結晶型cBN砥粒のようにへき
開などの大破壊を起こさず高い強度を示す。そのため、
砥石として使用した場合に優れた耐摩耗性を示す。多結
晶型cBN砥粒は、特公昭63-44417号公報及び特開平6-
240235号公報にも述べられているように、触媒を用いな
い無触媒直接転換法によって合成されたcBN焼結体を
所望の粒度に粉砕することによって製造される。しか
し、このような多結晶型cBN砥粒であっても実際に重
研削、高速研削などの過酷な条件下で砥石として用いる
と、耐摩耗性には優れるがドレッシング後の初期の研削
抵抗が著しく高くなってしまうという問題があった。The cBN abrasive grains used for the cBN grindstone are roughly classified into two types, a polycrystalline type and a single crystal type. Since the polycrystalline cBN abrasive grains have a polycrystalline structure in which fine cBN crystal grains are firmly bonded to each other, a large breakage such as cleavage occurs like single crystal type cBN abrasive grains in which one particle is composed of a single crystal. It shows high strength without causing for that reason,
Shows excellent wear resistance when used as a grindstone. Polycrystalline cBN abrasive grains are disclosed in JP-B-63-44417 and JP-A-6-
As described in 240235, it is produced by crushing a cBN sintered body synthesized by a catalyst-free direct conversion method without using a catalyst into a desired particle size. However, even if such a polycrystalline cBN abrasive grain is actually used as a grindstone under severe conditions such as heavy grinding and high speed grinding, the abrasion resistance is excellent, but the initial grinding resistance after dressing is remarkable. There was the problem of becoming expensive.
【0006】一方、単結晶型cBN砥粒は、基本的に粒
子一つが単結晶により構成されているので、耐摩耗性に
は劣るが、へき開などの大破壊を起こすので鋭利なへき
開面が刃先にでやすく切れ味に優れるという特徴があ
る。単結晶型cBN砥粒は、特公昭38-14 号公報にも述
べられているように触媒を用いて合成されたcBN焼結
体から製造される。しかし、このような単結晶型cBN
砥粒であっても実際に重研削、高速研削などの過酷な条
件下で砥石として用いると、ドレッシング後の初期の研
削抵抗はかなり高く、また砥粒強度が小さく目こぼれが
起こるためか研削の進行にともない一旦低下した研削抵
抗が再度上昇し、頻繁に再ドレッシングを行なわなけれ
ばならないという問題があった。On the other hand, the single crystal type cBN abrasive grain is basically inferior in wear resistance because one particle is composed of a single crystal, but it causes a large breakage such as cleavage, so that a sharp cleavage surface has a cutting edge. It is characterized by being easy to dry and excellent in sharpness. The single crystal cBN abrasive grains are produced from a cBN sintered body synthesized by using a catalyst as described in Japanese Patent Publication No. 38-14. However, such single-crystal cBN
Even if the abrasive grains are actually used as a grindstone under severe conditions such as heavy grinding and high-speed grinding, the initial grinding resistance after dressing is considerably high, and the abrasive grain strength is small and spills may occur, which may cause grinding. Along with the progress, the grinding resistance, which had once decreased, rises again, and there has been a problem that frequent redressing has to be performed.
【0007】[0007]
【発明が解決しようとする課題】本発明の目的は、重研
削、高速研削などの過酷な使用条件下で研削抵抗が安定
して小さく、特に初期の研削抵抗を小さくし、しかも耐
摩耗性の大きい研削砥石を製作することのできる砥粒を
提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a stable and small grinding resistance under heavy use conditions such as heavy grinding and high speed grinding, and particularly to reduce initial grinding resistance and wear resistance. An object is to provide abrasive grains capable of producing a large grinding wheel.
【0008】本発明者らは、研削抵抗が安定して小さ
く、しかも耐摩耗性の大きい砥粒を開発すべく種々検討
した結果、酸素含有量を制御した多結晶型cBN砥粒と
単結晶型cBN砥粒を含む砥粒を用いた砥石が研削抵抗
が安定して小さくなり、しかも耐摩耗性に優れることを
見いだし、本発明を完成させたものである。As a result of various investigations by the present inventors to develop an abrasive grain having a stable grinding resistance and a small abrasion resistance, a polycrystalline cBN abrasive grain in which the oxygen content is controlled and a single crystal type are obtained. The present invention has been completed by finding that a grindstone using abrasive grains containing cBN abrasive grains has a stable grinding resistance and a small abrasion resistance and is excellent in wear resistance.
【0009】すなわち、酸素含有量の異なるさまざまな
多結晶型cBN砥粒と単結晶型cBN砥粒を種々の比率
で含有させた砥石で実際に重研削を行い研削の前後で砥
石表面に突き出している砥粒一つ一つの状態を観察した
結果、(1)酸素含有量0.10モル%以下の多結晶型
cBN砥粒は摩滅や大破壊が起きていないこと、(2)
酸素含有量0.10モル%以下の多結晶型cBN砥粒で
囲まれている単結晶型cBN砥粒はそれを単独で用いた
場合に比べて摩滅や大破壊が起きておらず鋭利な刃先が
保たれていること、を見いだした。また、実施例で詳述
するように、酸素含有量0.10モル%以下の多結晶型
cBN砥粒又は単結晶型cBN砥粒を単独で用いた砥石
に比べて初期の研削抵抗が著しく小さくかつ安定し、し
かも耐摩耗性も酸素含有量0.10モル%以下の多結晶
型cBN砥粒を単独で用いた場合に比べて遜色のないこ
とを見いだしたものである。That is, with a grindstone containing various polycrystalline type cBN abrasive grains having different oxygen contents and single crystal type cBN abrasive grains in various ratios, heavy grinding was actually carried out, and protrusions were made on the surface of the grindstone before and after grinding. As a result of observing the state of each of the present abrasive grains, (1) that the polycrystalline cBN abrasive grains having an oxygen content of 0.10 mol% or less have not been worn or destroyed (2)
The single crystal cBN abrasive grains surrounded by the polycrystalline cBN abrasive grains having an oxygen content of 0.10 mol% or less do not cause abrasion or large destruction as compared with the case where they are used alone, and have a sharp cutting edge. Was found to be maintained. Further, as will be described in detail in Examples, the initial grinding resistance is significantly smaller than that of a grindstone in which a polycrystalline cBN abrasive grain having an oxygen content of 0.10 mol% or less or a single crystal type cBN abrasive grain is used alone. It has been found that it is stable and has wear resistance comparable to the case where a polycrystalline cBN abrasive grain having an oxygen content of 0.10 mol% or less is used alone.
【0010】[0010]
【課題を解決するための手段】すなわち、本発明は、酸
素含有量0.10モル%以下の多結晶型cBN砥粒と単
結晶型cBN砥粒とを含むことを特徴とする砥粒であ
る。That is, the present invention is an abrasive grain characterized by containing polycrystalline cBN abrasive grains having an oxygen content of 0.10 mol% or less and single crystal type cBN abrasive grains. .
【0011】[0011]
【発明の実施の形態】以下、本発明についてさらに詳し
く説明する。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in more detail.
【0012】本発明において、多結晶型cBN砥粒の酸
素含有量は、たとえば多結晶型cBN砥粒を不活性ガス
中で溶融分解し、発生する酸素をカーボンと反応させる
ことにより二酸化炭素となし、それをガスクロマトグラ
フにより分析定量するインパルス融解熱伝導法を用いて
分析することができる。また、多結晶型cBN砥粒の酸
素の存在形態は、たとえば微小部分析装置付き透過電子
顕微鏡による成分分析と構造解析を併用することによっ
て行なうことができる。In the present invention, the oxygen content of the polycrystalline cBN abrasive grains is made into carbon dioxide by, for example, melting and decomposing the polycrystalline cBN abrasive grains in an inert gas and reacting the generated oxygen with carbon. , Which can be analyzed using an impulse melting heat conduction method in which it is analyzed and quantified by gas chromatography. The presence of oxygen in the polycrystalline cBN abrasive grains can be determined, for example, by using both component analysis and structural analysis using a transmission electron microscope equipped with a micro-part analysis device.
【0013】本発明において、多結晶型cBN砥粒の酸
素含有量を0.10モル%以下と限定したのは、0.1
0モル%を越える酸素含有量の多結晶型cBN砥粒では
靭性が低いためか、単結晶型cBN砥粒と混合して砥石
とした場合に耐摩耗性が著しく低下するからである。In the present invention, the oxygen content of the polycrystalline cBN abrasive grains is limited to 0.10 mol% or less.
This is because the polycrystalline cBN abrasive grains having an oxygen content of more than 0 mol% have a low toughness, and the abrasion resistance is significantly reduced when the abrasive grains are mixed with the single crystal cBN abrasive grains.
【0014】本発明で使用される酸素含有量0.10モ
ル%以下の多結晶型cBN砥粒は、たとえば以下のよう
にして入手することができる。すなわち、多結晶型cB
N焼結体は上記したように、触媒を用いない無触媒直接
転換法によって合成されたcBN焼結体を所望の粒度に
粉砕することによって製造することができる。その直接
転換cBN焼結体の合成法は、広く一般に知られてお
り、例えば特開平6-240235号公報に述べられているよう
に、熱分解窒化ほう素をcBNの安定領域である高温/
高圧下で処理することによって合成することである。所
望の酸素含有量を持つ多結晶型cBN砥粒を得るには、
たとえば特開平6-240235号公報に述べられているように
原料と反応室を制御することである。The polycrystalline cBN abrasive grains having an oxygen content of 0.10 mol% or less used in the present invention can be obtained, for example, as follows. That is, polycrystalline cB
As described above, the N sintered body can be produced by crushing the cBN sintered body synthesized by the catalyst-free direct conversion method without using a catalyst into a desired particle size. A method for synthesizing the direct conversion cBN sintered body is widely known. For example, as described in Japanese Patent Laid-Open No. 6-240235, pyrolytic boron nitride is used at a high temperature / high temperature which is a stable region of cBN.
It is to synthesize by treating under high pressure. To obtain a polycrystalline cBN abrasive grain having a desired oxygen content,
For example, as described in JP-A-6-240235, controlling the raw materials and reaction chamber.
【0015】本発明で使用される単結晶型cBN砥粒と
は、基本的に粒子一つが一つの単結晶により構成される
ものであるが、完全な単結晶ばかりを指すものではな
く、双晶や数十μm単位の大きな一次結晶粒子が結合し
たものも含まれる。The single crystal type cBN abrasive grain used in the present invention is basically composed of one single crystal, but it does not mean only a complete single crystal but a twin crystal. It also includes particles in which large primary crystal particles of several tens of μm unit are combined.
【0016】本発明で使用される単結晶型cBN砥粒
は、広く一般に市販されているので、市場で入手するこ
ともできるし、また、特公昭38-14 号公報にも述べられ
ているように、六方晶系の窒化ほう素に触媒を加えcB
Nの安定領域である高温/高圧下で処理することによっ
ても得ることができる。Since the single crystal type cBN abrasive grains used in the present invention are widely and generally commercially available, they can be obtained on the market or as described in Japanese Patent Publication No. 38-14. In addition, a catalyst was added to hexagonal boron nitride to produce cB.
It can also be obtained by treating under a high temperature / high pressure which is a stable region of N 2.
【0017】本発明の砥粒は、上記した酸素含有量0.
10モル%以下の多結晶型cBN砥粒と単結晶型cBN
砥粒とを一般的な方法で混合することによって製造する
ことができる。混合に際しては、ミキサーやホモジナイ
ザーを用いると均一な混合物が得られるので好適であ
る。また、ダイヤモンド、アルミナ、シリコンカーバイ
ド等の第三成分を加えることもできる。The abrasive grains of the present invention have an oxygen content of 0.
Polycrystalline cBN abrasive grains of 10 mol% or less and single crystalline cBN
It can be produced by mixing with abrasive grains in a conventional manner. Upon mixing, it is preferable to use a mixer or a homogenizer because a uniform mixture can be obtained. Also, a third component such as diamond, alumina, or silicon carbide can be added.
【0018】多結晶型cBN砥粒と単結晶型cBN砥粒
の混合比としては、砥粒全体に占める単結晶型cBN砥
粒の比率が20〜90重量%であることが好ましい。単
結晶型cBN砥粒の比率が20重量%未満では研削抵抗
の改善効果が小さくなり、また90重量%を越えると耐
摩耗性の改善効果が小さくなる。As a mixing ratio of the polycrystalline cBN abrasive grains and the single crystal type cBN abrasive grains, the ratio of the single crystal type cBN abrasive grains to the whole abrasive grains is preferably 20 to 90% by weight. If the ratio of the single crystal type cBN abrasive grains is less than 20% by weight, the effect of improving the grinding resistance becomes small, and if it exceeds 90% by weight, the effect of improving the wear resistance becomes small.
【0019】[0019]
【作用】本発明の砥粒を用いた砥石が、研削抵抗が安定
して小さくかつ耐摩耗性に優れる理由としては以下のこ
とが考えられる。The reason why the grindstone using the abrasive grains of the present invention has a stable and small grinding resistance and is excellent in wear resistance is considered as follows.
【0020】まず、研削抵抗が安定して小さい理由は次
のように考えられる。研削抵抗は、たとえば「研削加工
と砥粒加工」(1984年 共立出版発行)でも述べら
れているように、研削に作用する砥石表面上の砥粒先端
の鋭さが大きく影響することが知られている。すなわ
ち、砥石表面に存在する砥粒の先端が鋭利なほど研削抵
抗が小さくなる傾向がある。単結晶型cBN砥粒は、へ
き開破壊により砥粒先端が鋭利になりやすいが、強度が
劣るため研削中に大破壊を起こし研削に作用する砥粒数
が減少してしまう。一方、多結晶型cBN砥粒は、強度
が大きいため作用砥粒数の減少は小さいが、大きな破壊
が起きにくく摩滅的に摩耗するため形状が鋭利にならな
い。砥石表面に両砥粒が共存すると、強度の大きい多結
晶型cBN砥粒によって単結晶型cBN砥粒が保護され
るような状態となるため、鋭利な刃先を有する単結晶型
cBN砥粒の切れ刃数の減少が小さくなる。また、同時
に、多結晶型cBN砥粒の先端には、多結晶型cBN砥
粒のみを用いた場合よりも大きな負荷がかかるため適度
な破壊が起こり、通常の多結晶型cBN砥粒では起こり
にくい鋭利な切れ刃の生成が起こるものと思われる。こ
のように、両砥粒が砥石表面に共存すると両砥粒の相乗
効果によって切れ味に優れる鋭利な砥粒刃先が多く発生
し研削抵抗が安定して小さくなるものと考えられる。First, the reason why the grinding resistance is stable and small is considered as follows. It is known that the grinding resistance is greatly affected by the sharpness of the tip of the abrasive grain on the surface of the grindstone that acts on the grinding, as described in, for example, "Grinding and Abrasive Machining" (published by Kyoritsu Shuppan, 1984). There is. That is, the sharper the tips of the abrasive grains present on the surface of the grindstone, the smaller the grinding resistance tends to be. The single crystal cBN abrasive grains tend to be sharp at the tip of the abrasive grains due to cleavage breakage, but since the strength is poor, large breakage occurs during grinding and the number of abrasive grains acting on grinding decreases. On the other hand, since the polycrystalline cBN abrasive grains have a large strength, the decrease in the number of working abrasive grains is small, but a large breakage is less likely to occur, and the abrasive grains are abraded, so that the shape is not sharp. When both abrasive grains coexist on the surface of the grindstone, the polycrystalline cBN abrasive grains with high strength protect the single crystal type cBN abrasive grains. Therefore, the cutting of the single crystal type cBN abrasive grains having a sharp cutting edge is performed. The decrease in the number of blades becomes smaller. At the same time, a larger load is applied to the tips of the polycrystalline cBN abrasive grains than in the case where only the polycrystalline cBN abrasive grains are used, so that moderate fracture occurs, which is unlikely to occur with ordinary polycrystalline cBN abrasive grains. It seems that the formation of sharp cutting edges occurs. As described above, when both abrasive grains coexist on the surface of the grindstone, it is considered that due to the synergistic effect of both abrasive grains, a large number of sharp abrasive grain cutting edges having excellent sharpness are generated and the grinding resistance is stably reduced.
【0021】次に、多結晶型cBN砥粒を単独に用いた
場合と遜色のない優れた耐摩耗性を示す理由としては以
下のことが考えられる。本発明の砥粒を用いた砥石の表
面には強度が大きく耐摩耗性の大きい多結晶型cBN砥
粒と、強度の小さい単結晶型cBN砥粒が混ざり合った
状態で、多数、砥粒の一部を突き出した状態で存在して
いる。研削前には、両者の突き出し高さはほぼ同一であ
るが、研削中にはこれらの砥粒の先端部には被削材との
衝突で衝撃的な力が作用する。研削を開始するとその初
期には両者に同等の衝撃力が作用する。しかしながら、
単結晶型cBN砥粒はへき開破壊を起こしやすいために
先端部が破壊し突き出し高さが低くなるのに対し、多結
晶型cBN砥粒は強度が大きいためにその突き出し高さ
をある程度保持している。単結晶型cBN砥粒の周りに
それよりも突き出した多結晶型cBN砥粒が存在するた
めに単結晶型cBN砥粒に作用する衝撃力は小さくな
り、単結晶型cBN砥粒の先端部の破壊はそれ以上進ま
なくなる。また、多結晶型cBN砥粒にとっても、周囲
に切れ味に優れた単結晶型cBN砥粒がある程度の突き
出し高さを維持した状態で存在しているので負荷が低減
され、両砥粒の相乗効果によって砥石の耐摩耗性が向上
するものと思われる。Next, the reason for showing excellent wear resistance comparable to the case where the polycrystalline cBN abrasive grains are used alone is considered as follows. On the surface of a grindstone using the abrasive grains of the present invention, polycrystalline cBN abrasive grains having high strength and high wear resistance and single crystal type cBN abrasive grains having low strength are mixed, and a large number of abrasive grains It exists with a part protruding. Before the grinding, the protrusion heights of the both are almost the same, but during grinding, a shocking force acts on the tips of these abrasive grains due to the collision with the work material. When grinding is started, the same impact force acts on both at the initial stage. However,
The single crystal type cBN abrasive grains are prone to cleavage fracture and the tip portion is broken to lower the protrusion height, whereas the polycrystalline cBN abrasive grains have high strength and therefore the protrusion height is maintained to some extent. There is. Since the polycrystalline cBN abrasive grains protruding further than the single crystal cBN abrasive grains are present, the impact force acting on the single crystal cBN abrasive grains becomes small, and the tip portion of the single crystal cBN abrasive grains becomes smaller. Destruction does not proceed any further. Further, for the polycrystalline cBN abrasive grains, the load is reduced because the single crystal type cBN abrasive grains with excellent sharpness are present around the periphery while maintaining a certain protrusion height, and the synergistic effect of both abrasive grains is achieved. It is believed that this improves the wear resistance of the grindstone.
【0022】[0022]
【実施例】次に、実施例を挙げてさらに具体的に本発明
を説明する。EXAMPLES Next, the present invention will be described more specifically by way of examples.
【0023】実施例1〜8 比較例1〜2 特開平6-240235号公報に述べられている方法を用い、さ
まざまな酸素含有量の多結晶型cBN砥粒を以下に従っ
て製造した。Examples 1 to 8 Comparative Examples 1 to 2 Using the method described in Japanese Patent Laid-Open No. 6-240235, polycrystalline cBN abrasive grains having various oxygen contents were manufactured as follows.
【0024】すなわち、原料の脱酸素処理を行なうた
め、純度99.9%以上の熱分解窒化ほう素を純度9
9.9%以上の高純度カーボン中に封入した後、窒素雰
囲気中、温度800℃で30〜90分間のさまざまな時
間に保持して熱処理した。得られた熱分解窒化ほう素を
カーボンに封入したまま上記高純度カーボンを加熱用ヒ
ーターとする構造の反応セル中に配置し、フラットベル
ト型超高圧高温発生装置に装填し、温度2100℃、圧
力7.3GPa下、60分間処理する直接転換法によ
り、さまざまな酸素含有量の多結晶型cBN焼結体を合
成した。これをロールクラッシャーで粉砕した後、分級
して100/120メッシュの砥粒を選別した。That is, in order to deoxidize the raw material, a pyrolytic boron nitride having a purity of 99.9% or more is used.
After encapsulating in 9.9% or more high-purity carbon, it was heat-treated in a nitrogen atmosphere at a temperature of 800 ° C. for various times of 30 to 90 minutes. The obtained pyrolytic boron nitride was enclosed in carbon, placed in a reaction cell having a structure using the above-mentioned high-purity carbon as a heater for heating, and loaded in a flat-belt type ultra-high pressure and high temperature generator, at a temperature of 2100 ° C. and pressure. Polycrystalline cBN sintered bodies with various oxygen contents were synthesized by a direct conversion method of treating at 7.3 GPa for 60 minutes. This was crushed by a roll crusher and then classified to select 100/120 mesh abrasive grains.
【0025】この砥粒から、JISR6003の方法で
1.2gをサンプリングし、インパルス炉中に入れて加
熱し、溶融分解して発生する酸素をカーボン酸化によっ
て二酸化炭素となし、それをガスクロマトグラフにより
定量することによって砥粒中の酸素のモル%を算出し
た。その結果を表1に示す。From this abrasive grain, 1.2 g was sampled by the method of JIS R6003, put in an impulse furnace and heated, and oxygen generated by melting and decomposition was converted to carbon dioxide by carbon oxidation, which was quantified by gas chromatography. By doing so, the mol% of oxygen in the abrasive grains was calculated. Table 1 shows the results.
【0026】次に、単結晶型cBN砥粒として市販品
〔ゼネラルエレクトリック社製「ボラゾンTYPE
I」(粒度100/120メッシュ)〕を入手し、上記
の多結晶型cBN砥粒と所望の混合比(重量比)でロッ
キングミキサー(愛知電機商事社製)を用いて混合し
た。Next, as a single-crystal type cBN abrasive grain, a commercially available product ["Borazon TYPE manufactured by General Electric Co., Ltd.
I ”(particle size 100/120 mesh)] was obtained and mixed with the above-mentioned polycrystalline cBN abrasive grains at a desired mixing ratio (weight ratio) using a rocking mixer (manufactured by Aichi Denki Shoji Co., Ltd.).
【0027】混合された砥粒から100カラットを抜き
出し、直径200mm、厚さ10mm、集中度100の
メタルボンド砥石を作製した。この砥石を用い平面プラ
ンジカット法で研削試験を行い、研削抵抗として各研削
体積における砥石軸電流値及び砥石摩耗量を測定した。
それらの結果を表1に示す。なお、試験に用いた被削材
は高速度工具鋼SKH−51(ロックウェル硬度:65
度)であり、研削条件は砥石周速度1800m/mi
n、被削材送り速度9m/min、砥石切込み量15μ
mである。100 carats was extracted from the mixed abrasive grains to prepare a metal bond grindstone having a diameter of 200 mm, a thickness of 10 mm and a concentration of 100. A grinding test was performed using this grindstone by a plane plunge cut method, and a grindstone axial current value and a grindstone wear amount in each grinding volume were measured as grinding resistance.
Table 1 shows the results. The work material used in the test was high speed tool steel SKH-51 (Rockwell hardness: 65).
And the grinding condition is a grinding wheel peripheral speed of 1800 m / mi
n, work material feed rate 9 m / min, grindstone cutting amount 15 μ
m.
【0028】比較例3 脱酸素処理を行なわなかった熱分解窒化ほう素原料を用
いたこと以外は、実施例1に準じて多結晶型cBN砥粒
を製造し評価試験を行なった。それらの結果を表1に示
す。Comparative Example 3 Polycrystalline cBN abrasive grains were manufactured and evaluated in the same manner as in Example 1 except that a pyrolytic boron nitride raw material that was not deoxidized was used. Table 1 shows the results.
【0029】[0029]
【表1】 (注)研削抵抗の初期値:10mm3 /mm研削後の値 研削抵抗の中期値:7,000mm3 /mm研削後の値 研削抵抗の後期値:14,000mm3 /mm研削後の値[Table 1] (Note) Initial value of grinding resistance: 10 mm 3 / mm Value after grinding Medium value of grinding resistance: 7,000 mm 3 / mm Value after grinding Late value of grinding resistance: 14,000 mm 3 / mm Value after grinding
【0030】[0030]
【発明の効果】本発明の砥粒によれば、研削抵抗が安定
して小さく、しかも耐摩耗性に優れた高性能な研削砥石
を製作することができる。According to the abrasive grains of the present invention, it is possible to manufacture a high-performance grinding wheel having a stable grinding resistance and a small wear resistance.
Claims (1)
型立方晶窒化ほう素砥粒と単結晶型立方晶窒化ほう素砥
粒とを含むことを特徴とする砥粒。1. An abrasive grain comprising a polycrystalline cubic boron nitride abrasive grain having an oxygen content of 0.10 mol% or less and a single crystal cubic boron nitride abrasive grain.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18897795A JPH0931445A (en) | 1995-07-25 | 1995-07-25 | Grinding grain |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18897795A JPH0931445A (en) | 1995-07-25 | 1995-07-25 | Grinding grain |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0931445A true JPH0931445A (en) | 1997-02-04 |
Family
ID=16233244
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18897795A Pending JPH0931445A (en) | 1995-07-25 | 1995-07-25 | Grinding grain |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0931445A (en) |
-
1995
- 1995-07-25 JP JP18897795A patent/JPH0931445A/en active Pending
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