JPH0138628B2 - - Google Patents
Info
- Publication number
- JPH0138628B2 JPH0138628B2 JP56180991A JP18099181A JPH0138628B2 JP H0138628 B2 JPH0138628 B2 JP H0138628B2 JP 56180991 A JP56180991 A JP 56180991A JP 18099181 A JP18099181 A JP 18099181A JP H0138628 B2 JPH0138628 B2 JP H0138628B2
- Authority
- JP
- Japan
- Prior art keywords
- cbn
- aggregate
- superabrasive
- grains
- grinding
- 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.)
- Expired
Links
- 238000000227 grinding Methods 0.000 claims description 60
- 239000006061 abrasive grain Substances 0.000 claims description 45
- 239000002245 particle Substances 0.000 claims description 36
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 claims description 21
- 229910052863 mullite Inorganic materials 0.000 claims description 21
- 229910003460 diamond Inorganic materials 0.000 claims description 18
- 239000010432 diamond Substances 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 10
- 239000000919 ceramic Substances 0.000 claims description 6
- 238000010304 firing Methods 0.000 claims description 6
- 229910052845 zircon Inorganic materials 0.000 claims description 5
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 5
- 229910052582 BN Inorganic materials 0.000 claims description 4
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 4
- 229910052878 cordierite Inorganic materials 0.000 claims description 4
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000013078 crystal Substances 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 description 13
- 239000000463 material Substances 0.000 description 11
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 10
- 229910010271 silicon carbide Inorganic materials 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 8
- 230000007423 decrease Effects 0.000 description 7
- 230000014759 maintenance of location Effects 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 238000005452 bending Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 230000002093 peripheral effect Effects 0.000 description 3
- 238000005245 sintering Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000003292 glue Substances 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 230000010355 oscillation Effects 0.000 description 2
- 238000013001 point bending Methods 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- HEHRHMRHPUNLIR-UHFFFAOYSA-N aluminum;hydroxy-[hydroxy(oxo)silyl]oxy-oxosilane;lithium Chemical compound [Li].[Al].O[Si](=O)O[Si](O)=O.O[Si](=O)O[Si](O)=O HEHRHMRHPUNLIR-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910000174 eucryptite Inorganic materials 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052670 petalite Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D3/00—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
- B24D3/02—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
- B24D3/04—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic
- B24D3/14—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic ceramic, i.e. vitrified bondings
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Inorganic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Polishing Bodies And Polishing Tools (AREA)
- Ceramic Products (AREA)
Description
本発明は立方晶窒化ホウ素(CBN)又はダイ
ヤモンド等の超砥粒及びムライト・ジルコン等の
骨材をガラス質又はセラミツク質のボンドで結合
した超砥粒ビトリフアイド研削砥石に関する。
超砥粒のみを砥粒としたビトリフアイド超砥粒
砥石は慣用されているが、超砥粒に普通砥粒を混
合した砥石は色々その効果が提案されてはいるも
のゝ一部の例外を除き、種々の困難のため実用化
されていない。例えば立方晶窒化ホウ素(以下
CBNと略記する)をガラス質、結晶質またはセ
ラミツク質のボンドで結合してビトリフアイド砥
石を製造する場合、一般砥粒の約1万倍という
CBN砥粒の高コストを幾分でも低減するため特
公昭52―3147に記されている如く、CBNを単独
で用いる以外にアルミナ質砥粒とともに用いるこ
とにより、CBN砥粒の濃度を下げ各種低集中度
の砥石を供する事が行なわれている。また、特公
昭52―27394においてはジルコン、ムライト、コ
ーデイエライト、スポジウメン、β―ユークリプ
タイト、ペタライトの如き修正モース硬度11以
下、融点900℃以上の結晶を主成分とする骨材を
用いている。さらに、特公昭55―20826において
は溶融アルミナ又は炭化ケイ素等一般の砥材に小
量のCBNを混合して砥石としている。
これらの技術によつて製造されるビトリフアイ
ドCBN砥石は従来砥粒では研削不可能であつた
難削材の研削及び精密研削の分野で注目を浴びて
いるが一般鋼材の量産研削の場合CBN砥粒の集
中度を低くした場合砥粒の保持力が大幅に低下
し、CBN含有量に相当するよりはるかに下廻る
研削性能しか得られないことが多く安価な低集中
度CBN砥石を一般鋼材研削へ、経済的に適用す
る事が不可能に近かつた。例えば、アルミナ砥粒
とCBN砥粒を1:1に混合し集中度100とした
CBN砥石の研削比は、CBN単独の砥石(集中度
200)の1/2ならばCBN砥粒%に比例する性能が
得られたと言い得るが、実際には集中度200の砥
石の数分の1の研削比しかえられない事が多かつ
た。即ち超砥粒の集中度相応の研削性能をうるこ
とが不可能であつた。この為低集中度で優れた研
削比をもつ経済的なCBN砥石の出現が望まれて
いた。本発明は集中度を下げる事による砥粒保持
力(結合強度)の低下をなくすとともに超砥粒の
特性を生かし、超砥粒含有量相当以上の研削性能
を示す高性能砥石を提供せんとするものである。
即ち、本発明は、CBN、ダイヤモンド等の超
砥粒を砥粒とするビトリフアイド研削砥石におい
て熱膨張係数が超砥粒の熱膨張係数に対し、±2.0
×10-6K-1である酸化物粒子から成る骨材を超砥
粒/骨材比90/10〜10/90容量比配合し、ビトリ
フアイドボンドにより焼結して成る超砥粒砥石を
提供する。
以下本発明について詳述する。
前述の従来法の欠点について研究した結果、以
下の事実を究明した。
即ち、ビトリフアイドボンドは焼成の昇温過程
において溶融され第1図に示す如く砥粒間にボン
ドブリツジを形成する。ついで冷却過程に入ると
CBN粒とアルミナ砥粒等の骨材粒との熱膨張差
に起因する剪断応力が粒表面に平行に、即ちボン
ドブリツジを分断する方向に発生する。その応力
が大きい場合には、ボンドブリツジに粒面に平行
なクラツクを生じ、砥粒保持力が低下する。
CBN等の超砥粒にアルミナ砥粒等の普通砥粒を
混合した場合、超砥粒/普通砥粒の配合比が50/
50に近づくに従い上記クラツクが多くなり全体と
して砥石の砥粒保持力を低下させることが明らか
となつた。さらに砥粒保持力に影響を及ぼす要因
として砥粒及び骨材のビトリフアイドボンドとの
親和性がある。親和性が良好なほど砥粒保持力が
高く一般にビトリフアイドボンドは、酸化物・硼
化物には親和性が良いが、SiC等炭化物には親和
性がとぼしい。
一方、骨材の粒径も砥石摩耗形態に影響を及ぼ
す。例えば、CBN砥粒に比して粒径の大きな骨
材を用いた場合、骨材の脱落に伴いCBN砥粒も
脱落すると考えられ、事実砥石が摩耗し易く芳し
くない。
本発明者は特に骨材の熱膨張係数に着目し、さ
らに親和性、粒径をも加味して研究の結果ムライ
ト、ジルコン等の熱膨張係数がCBN、ダイヤモ
ンド等超砥粒の常温〜500℃間の熱膨張係数に対
し±2.0×10-6K-1以内でかつ粒径がCBN砥粒の
粒径の20〜100%である酸化物粒子を用いること
により、低集中度による砥粒保持力の低下をなく
し、集中度相当以上の性能をもつ高性能砥石を開
発するに至つた。例えば集中度100の砥石で集中
度200の砥石の60%〜100%の研削性能を示す高性
能砥石が得られた。
超砥粒はCBN、及び又はダイヤモンド砥粒を
用いるが、一般に鉄系の材料の研削にはCBN砥
粒が好まれる。CBN又はダイヤモンド砥粒の常
温〜500℃間の熱膨張係数に対し、添加する酸化
物粒子骨材のそれは差が±2.0×10-6K-1以内のも
の、好ましくは±1.5×10-6K-1以内のものを用い
る。差がこの範囲をこえると、ボンドクラツクが
生成かつ増大して、砥粒保持力が低下する。この
差以内では従来見られた超砥粒集中度100の付近
での保持力の劣化による極小値がみられなくな
り、従来の超砥粒配合量相応以下の研削比しか得
られないという問題点が解消したに止まらず、超
砥粒配合量相応以上の研削比を持つ高性能砥石が
得られる。
砥石中の配合率、超砥粒/骨材粒比90/10〜
10/90容量比は超砥粒単独に近いものが及び超砥
粒の極めて少量の場合を除いたほかの配合率の場
合に特に性能的及び経済的に顕著な効果を示すと
いう意義であり、その範囲外でも、熱膨張率の
差、粒径差、親和性の選定により従来法に対し改
良が可能であることは当然である。
上記配合率範囲内で、被研削物、砥石コスト等
目的に応じて骨材と超砥粒の配合率を選ぶ。
なお、砥石中における超砥粒と骨材との合量
は、通例凡そ30〜60容量%であり、好ましくは40
〜55容量%であるが、適宜目的に応じて定めるも
のである。
酸化物粒子骨材としては、1200℃以上の耐火度
を有し、かつ、砥石焼成時にビトリフアイドボン
ドにより溶解されないセラミツク粒子を用い、例
えば、溶融ムライト、ジルコン、実質的に、ムラ
イト結晶から成るアルミナ―シリカ系セラミツク
ス、コーデイエライト、又はこれらの混合物を用
いることができる。
CBNの熱膨張係数は3.5×10-6K-1(室温〜500
℃)であり、ダイヤモンドは2.7×10-6K-1(室温
〜500℃)であるが、前掲の骨材は、熱膨張差の
条件をみたすことができる。さらに、前記骨材は
ボンドとの親和性に関する条件も充たしうる。
なお、種々の骨材の熱膨張係数を第1表に例示
する。
The present invention relates to a superabrasive vitrified grinding wheel in which superabrasive grains such as cubic boron nitride (CBN) or diamond and aggregates such as mullite or zircon are bonded together with a glassy or ceramic bond. Vitrified superabrasive grinding wheels that contain only superabrasive grains are commonly used, but a variety of effects have been proposed for grinding wheels that mix superabrasive grains with normal abrasive grains (with some exceptions). However, it has not been put into practical use due to various difficulties. For example, cubic boron nitride (hereinafter
When manufacturing a vitrified grinding wheel by bonding CBN (abbreviated as CBN) with a glassy, crystalline, or ceramic bond, the grinding speed is approximately 10,000 times that of general abrasive grains.
In order to reduce the high cost of CBN abrasive grains, as stated in Japanese Patent Publication No. 52-3147, instead of using CBN alone, it is also used together with alumina abrasive grains to lower the concentration of CBN abrasive grains and reduce the concentration of CBN abrasive grains. It is being done to provide a whetstone for concentration. In addition, in Japanese Patent Publication No. 52-27394, aggregates mainly composed of crystals such as zircon, mullite, cordierite, spodiumene, β-eucryptite, and petalite with a modified Mohs hardness of 11 or less and a melting point of 900℃ or higher are used. There is. Furthermore, in Japanese Patent Publication No. 55-20826, a small amount of CBN is mixed with a general abrasive material such as fused alumina or silicon carbide to make a whetstone. Vitrified CBN grinding wheels manufactured using these technologies are attracting attention in the fields of grinding and precision grinding of difficult-to-cut materials that cannot be ground with conventional abrasive grains. When the concentration of CBN is lowered, the holding power of the abrasive grains decreases significantly, and the grinding performance is often much lower than that corresponding to the CBN content.Inexpensive low concentration CBN grinding wheels are often used for grinding general steel materials. , it was almost impossible to apply it economically. For example, alumina abrasive grains and CBN abrasive grains were mixed 1:1 and the concentration was 100.
The grinding ratio of CBN grinding wheel is as follows: CBN grinding wheel alone (concentration
200), it can be said that performance proportional to the CBN abrasive grain percentage was obtained, but in reality, the grinding ratio was often only a fraction of that of a grindstone with a concentration of 200. That is, it has been impossible to obtain grinding performance commensurate with the concentration of superabrasive grains. For this reason, it has been desired to develop an economical CBN grinding wheel with low concentration and excellent grinding ratio. The present invention aims to eliminate the decrease in abrasive grain retention (bonding strength) caused by lowering the degree of concentration, and to utilize the characteristics of superabrasive grains to provide a high-performance grindstone that exhibits grinding performance equivalent to or higher than the superabrasive grain content. It is something. That is, in the present invention, in a vitrified grinding wheel using superabrasive grains such as CBN or diamond, the coefficient of thermal expansion is ±2.0 with respect to the coefficient of thermal expansion of the superabrasive grains.
A super-abrasive grinding wheel made by blending aggregate consisting of oxide particles with × 10 -6 K -1 in a super-abrasive/aggregate ratio of 90/10 to 10/90 by volume and sintering it with a vitrified bond. I will provide a. The present invention will be explained in detail below. As a result of research into the drawbacks of the conventional method described above, the following facts were discovered. That is, the bitrified bond is melted during the heating process of firing and forms bond bridges between the abrasive grains as shown in FIG. Then, when the cooling process begins
Shear stress due to the difference in thermal expansion between CBN grains and aggregate grains such as alumina abrasive grains occurs parallel to the grain surfaces, that is, in the direction of dividing the bond bridge. If the stress is large, cracks parallel to the grain plane will occur in the bond bridge, reducing the abrasive grain retention.
When super abrasive grains such as CBN are mixed with normal abrasive grains such as alumina abrasive grains, the blending ratio of super abrasive grains/normal abrasive grains is 50/
It has become clear that as the value approaches 50, the number of cracks increases and the abrasive grain retention of the whetstone decreases as a whole. Furthermore, a factor that affects the abrasive grain retention is the affinity of the abrasive grains and aggregate with the vitrified bond. The better the affinity, the higher the abrasive retention.Generally, vitrified bond has good affinity for oxides and borides, but poor affinity for carbides such as SiC. On the other hand, the particle size of the aggregate also affects the wear pattern of the grinding wheel. For example, if aggregate with a larger particle size than CBN abrasive grains is used, it is thought that the CBN abrasive grains will also fall off as the aggregate falls off, and in fact the grindstone will easily wear out, which is not good. The present inventor focused on the coefficient of thermal expansion of aggregate, and also took into account affinity and particle size.As a result, the thermal expansion coefficient of mullite, zircon, etc. is higher than that of CBN, diamond, etc. By using oxide particles whose thermal expansion coefficient is within ±2.0×10 -6 K -1 and whose particle size is 20 to 100% of the CBN abrasive particle size, abrasive grain retention due to low concentration is achieved. We have developed a high-performance whetstone that eliminates the drop in power and has performance equivalent to or higher than that of concentration. For example, a high-performance grindstone with a concentration of 100 has a grinding performance of 60% to 100% of a grindstone with a concentration of 200. CBN and/or diamond abrasive grains are used as superabrasive grains, and CBN abrasive grains are generally preferred for grinding iron-based materials. The difference between the coefficient of thermal expansion of CBN or diamond abrasive grains between room temperature and 500℃ of the oxide particle aggregate to be added is within ±2.0×10 -6 K -1 , preferably ±1.5×10 -6 Use one within K -1 . If the difference exceeds this range, bond cracks will form and increase and the abrasive retention will decrease. Within this difference, the minimum value due to deterioration of holding force near the superabrasive concentration of 100, which was observed in the past, is no longer observed, and the problem is that a grinding ratio that is lower than that corresponding to the conventional superabrasive content can be obtained. Not only has the problem been solved, but a high-performance grinding wheel with a grinding ratio greater than that commensurate with the amount of superabrasive grains contained can be obtained. Compounding ratio in the whetstone, super abrasive grain/aggregate grain ratio 90/10~
The 10/90 capacity ratio means that something similar to superabrasive grains alone or a mixture ratio other than a very small amount of superabrasive grains exhibits a remarkable effect in terms of performance and economy. Even outside this range, it is of course possible to improve the conventional method by selecting the difference in thermal expansion coefficient, the difference in particle size, and the affinity. Within the above blending ratio range, the blending ratio of aggregate and superabrasive grains is selected depending on the object to be ground, the cost of the grinding wheel, etc. The total amount of superabrasive grains and aggregate in the grinding wheel is usually about 30 to 60% by volume, preferably 40% by volume.
~55% by volume, but may be determined depending on the purpose. As the oxide particle aggregate, use ceramic particles that have a fire resistance of 1200°C or higher and are not dissolved by bitrified bond during grindstone firing, such as molten mullite, zircon, or consisting essentially of mullite crystals. Alumina-silica ceramics, cordierite, or a mixture thereof can be used. The thermal expansion coefficient of CBN is 3.5×10 -6 K -1 (room temperature ~ 500
℃), and diamond has a temperature of 2.7×10 -6 K -1 (room temperature to 500°C), but the above-mentioned aggregate can satisfy the condition of differential thermal expansion. Furthermore, the aggregate may also satisfy conditions regarding affinity with bond. The thermal expansion coefficients of various aggregates are illustrated in Table 1.
【表】
ものから選
択する)
骨材の耐火度は1200℃以上とするが、これは焼
結時においてできる限り骨材の変形、割れ、溶
融、ボンド中への融け込み等による変化、変質を
避けるためである。これより低い耐火度では軟化
流動するガラス質又は結晶質ボンドが共存する焼
成に耐えられない。又、単味酸化物で耐火度1200
℃以上であつてもMgO,CaOの如く塩基性の強
いものは容易にビトリフアイドボンドに融け込む
為、骨材として不適である。
酸化物粒子骨材は、超砥粒の粒径に対し、20〜
100%、好ましくは40〜80%の粒径とする。この
骨材粒径の限定により、超砥粒の効果を害うこと
なく、骨材としての所期の効果を達成できる。骨
材粒径が100%をこえると、研削比は超砥粒配合
率相応より低下する。また、粒径が20%より小さ
いと骨材としての好ましい機能を果すことができ
ず、同じく研削比は超砥粒配合率相応より低下す
る。これらの関係はCBN/電融ムライトが50/
50容量比の場合を例示した第3図により明らかで
ある。
また、骨材として略球状ムライト質粒子を用い
た場合には、CBN砥粒と嵩比重が近似している
ため、集中度による焼成収縮の変化が少なく、特
願昭56―60645号に記載されている保持体部の適
用が容易となる。
なお、ボンドとの親和性の観点からSiC,B4C
等の炭化物系は、これらで熱膨張係数の条件を充
たすものであつても、好ましくない。なお、炭化
物は鉄との反応性の観点からも、一般に鉄材料の
研削目的には好まれない。
ホウ化物材料で、本発明の条件をみたすものも
あるが、但し、これらは、一般に高価なので、骨
材として配合することにより安価な砥石を提供す
るという場合にはふさわしくない。
なお、本発明に用いるビトリフアイドボンド
は、一般にCBN砥粒又はダイヤモンド砥粒を用
いた砥石に適したものを選択する。ビトリフアイ
ドボンドの砥石中の配合率は、従来法とほゞ同様
であり通例凡そ10〜30容量%程度でよいが、適宜
目的に応じて定めるものである。
以上の条件に従い、超砥粒に適当な骨材を配し
てビトリフアイド砥石を成形後焼成することによ
り、CBN又はダイヤモンド等の超砥粒単独の場
合の集中度200の砥石の研削性能の60%〜100%の
研削性能を備えたものを、超砥粒集中度100の砥
石において得ることができる。そのため一定の研
削性能に対する超砥粒の必要量が大幅に低減でき
る。さらに、本発明によれば、目的に応じた超砥
粒/骨材配合率の自由な砥石設計が可能となる。
特殊な目的に対してはCBN、ダイヤモンドの
両砥粒の混合砥石も可能である。アルミナと炭化
珪素砥粒の混合砥石は、両砥粒の膨張係数の著し
い差によりボンドにクラツクが入り強度が著しく
弱くなり、実用上問題があるが、CBNとダイヤ
モンドは膨張係数が近似する為混合砥石が可能で
ある。又、CBNとダイヤモンドを混合使用して、
骨材により超砥粒の含有率を下げる場合には、本
特許記載の電融ムライト等の骨材を用いる事によ
り、良好な研削性能をもつた低集中度の超砥粒コ
ンビ砥石の製造が可能である。
以下実施例を示す。
比較例 1[Table] Select from items
(choose)
The fire resistance of the aggregate should be 1200°C or higher, in order to avoid deformation, cracking, melting, melting of the aggregate, etc. during sintering as much as possible. A fire resistance lower than this cannot withstand firing in which glassy or crystalline bonds that soften and flow coexist. In addition, it is a simple oxide and has a fire resistance of 1200.
Strongly basic substances such as MgO and CaO are unsuitable as aggregates even at temperatures above ℃ because they easily melt into vitrified bond. The particle size of the oxide particle aggregate is 20~
The particle size should be 100%, preferably 40-80%. By limiting the particle size of the aggregate, the desired effect as an aggregate can be achieved without impairing the effect of the superabrasive grains. When the aggregate particle size exceeds 100%, the grinding ratio decreases relative to the superabrasive grain blending ratio. Furthermore, if the particle size is smaller than 20%, it will not be able to perform the desired function as an aggregate, and the grinding ratio will also be lower than the proportion corresponding to the superabrasive grain content. These relationships are CBN/fused mullite 50/
This is clear from FIG. 3, which illustrates the case of a 50 capacity ratio. In addition, when approximately spherical mullite particles are used as the aggregate, the bulk specific gravity is similar to that of CBN abrasive grains, so there is little change in firing shrinkage due to the degree of concentration. This makes it easy to apply the holding body part. In addition, from the viewpoint of compatibility with bond, SiC, B 4 C
Carbide systems such as these are not preferred even if they satisfy the thermal expansion coefficient conditions. Note that carbides are generally not preferred for the purpose of grinding iron materials, also from the viewpoint of reactivity with iron. There are some boride materials that meet the requirements of the present invention, but these are generally expensive and are not suitable for providing an inexpensive grindstone by blending them as aggregate. Note that the bitrified bond used in the present invention is generally selected to be suitable for a grindstone using CBN abrasive grains or diamond abrasive grains. The blending ratio of vitrified bond in the grindstone is almost the same as in the conventional method, and is usually about 10 to 30% by volume, but it is determined as appropriate depending on the purpose. According to the above conditions, by arranging appropriate aggregates on superabrasive grains, forming and firing a vitrified grinding wheel, the grinding performance of a grinding wheel with a concentration of 200 obtained by using CBN or diamond alone can be reduced to 60%. A grinding performance of ~100% can be obtained in a wheel with a superabrasive concentration of 100. Therefore, the amount of superabrasive required for a given grinding performance can be significantly reduced. Further, according to the present invention, it is possible to freely design a grindstone with a superabrasive/aggregate blend ratio depending on the purpose. For special purposes, a mixture of CBN and diamond abrasive grains is also available. A grinding wheel containing a mixture of alumina and silicon carbide abrasive grains has a practical problem as the bond cracks and its strength is significantly weakened due to the significant difference in the expansion coefficients of the two abrasive grains, but CBN and diamond are mixed because their expansion coefficients are similar. A grindstone is possible. Also, by using a mixture of CBN and diamond,
When reducing the content of superabrasive grains by using aggregate, it is possible to manufacture a superabrasive combination grindstone with a low concentration and good grinding performance by using aggregates such as fused mullite described in this patent. It is possible. Examples are shown below. Comparative example 1
【表】 比較例 2【table】 Comparative example 2
【表】 実施例 1【table】 Example 1
【表】 実施例 2【table】 Example 2
【表】
上記比較例1,2、実施例1,2の各配合物
を、夫々長さ40mm幅4mm厚み6mmの角柱型にプレ
ス成形し950℃で5時間焼成して砥石を得た。こ
れらの砥石の強度を、スパン30mmクロスヘツドス
ピード1mm/minの条件で3点曲げにより測定し
た結果を第2図に示す。曲げ強度はCBN100容量
部の場合を1として相対値で示してある。
アルミナ砥粒の熱膨張係数は(7.4×10-6K-1)
で、CBNの熱膨張係数(常温〜500℃間、以下同
じ)(3.5×10-6K-1)との差が大きいため、ボン
ドブリツジにクラツクが生じていると考えられ、
第2図においてCBN―骨材間のボンドブリツジ
数が最も多くなると考えられる混合比50:50の点
で最低強度を示していることから、明らかであ
る。
一方、炭化ケイ素砥粒の熱膨張係数は4.2×
10-6K-1でCBNの熱膨張係数に近い値であるた
め、ボンドブリツジにクラツクを生ずることな
く、曲げ強度は混合比と直線関係を示している。
しかしビトリフアイドボンドとの親和性に欠ける
ため、炭化ケイ素砥粒の増加に伴ない強度が低下
している。
本発明によるムライトは熱膨張係数が4.5×
10-6K-1でCBNの熱膨張係数に対し±2.0×
10-6K-1以内であるとともに、ビトリフアイドボ
ンドとの親和性が良いため、混合比とは無関係に
高い水準の一定の強度を示す。また、コーデイエ
ライトの場合にもムライトと同様に一定の強度を
示している。
以上の様に骨材の熱膨張係数がCBNの熱膨張
係数に対し±2.0×10-6K-1であれば異種粒子間応
力によるボンドブリツジのクラツクは発生せず、
集中度に対して直線的な強度変化を示す。一方、
ビトリフアイドボンドとの親和性は骨材が、アル
ミナ、ムライト等酸化物の場合に良好であり高い
強度を示す。但し、酸化物以外でも粒子表面処理
あるいは粒子表面に形成された他の化合物により
ビトリフアイドボンドとの親和性が良好となる場
合には、本発明の適用が可能である。
実施例 3
配 合
CBN#80/100 50容量部
電融ムライト 50 〃
ビトリフアイドボンド*
32 〃
*(実施例1
と同じ)
糊 料 20 〃
電融ムライトの粒度はCBNの粒径の0.2,0.4,
0.6,0.8,1.0,1.2、倍の粒径を使用し、配合物
を外径25mm厚さ14mm、穴径11mmの円板型にプレス
成形し、1000℃で3時間焼成して砥石を得た。こ
れらの砥石を集中度200の砥石を比較対象として、
内面研削を行なつた結果を第3図に示す。研削条
件は下記の通りである。
研削条件
砥石周速度 2700m/min
加工物周速度 75m/min
切込速度 φ1mm/min
揺動数 160cpm
揺動速度 42m/min
取り代 φ0.5mm
被削材 SNCM―420H(HRc42)
被削材寸法 直径50mm×厚さ13mm×穴径30mm
第3図から明らかな様に、この集中度100の砥
石は骨材の粒度がCBN砥粒の粒度の20〜100%の
範囲において集中度200の砥石の1/2以上の研削性
能が得られた。特に骨材粒径が60%の場合には集
中度100で集中度200の砥石と同等の高性能が得ら
れた。
比較例 3
配 合
CBN#80/100 50容量部
骨 材 50 〃
ビトリフアイドボンド*
32 〃
*(実施例1
と同じ)
糊 料 20 〃
骨材としてはWA#150,GC#150を用い、実
施例3と同様にして砥石を製造し、研削試験を行
なつた結果を第4図に示す。
実施例 4
配 合
<CBN#80/100
電極ムライト> 100重量部
ビトリフアイドボンド 32 〃
糊 料 20 〃
CBNの配合量は、集中度50,100,150,200と
なる様変化させて、実施例3と同様にして砥石を
製造し、研削試験を行なつた結果を第4図に示
す。
第4図から明らかな様に溶融アルミナ、又は炭
化ケイ素を骨材として集中度100の砥石を作つた
場合、集中度200の砥石の約30〜40%以下の研削
比しか得られないのに対し、骨材として電融ムラ
イトを用いた場合は、最良のものは集中度100で
集中度200と同等の研削比が得られたのをはじめ
とし、いずれも、集中度相当の研削比(点線表示
の直線)を上回る高性能となつている。
以上の様に、骨材の熱膨張係数・親和性・粒度
を選択することにより、CBNの特性を十二分に
生かし、より高性能で、より安価なビトリフアイ
ドCBN研削砥石を提供することが可能である。
以下、超砥粒としてダイヤモンド砥粒を用いる
場合について比較例、実施例を示す。
比較例 4[Table] Each of the formulations of Comparative Examples 1 and 2 and Examples 1 and 2 was press-molded into a prismatic shape with a length of 40 mm, a width of 4 mm, and a thickness of 6 mm, and fired at 950° C. for 5 hours to obtain a grindstone. The strength of these grindstones was measured by three-point bending under conditions of a span of 30 mm and a crosshead speed of 1 mm/min. The results are shown in FIG. The bending strength is shown as a relative value, with the case of CBN 100 parts being 1. The thermal expansion coefficient of alumina abrasive grains is (7.4×10 -6 K -1 )
It is thought that cracks have occurred in the bond bridge due to the large difference between CBN's coefficient of thermal expansion (between room temperature and 500℃, the same applies hereinafter) (3.5×10 -6 K -1 ).
This is clear from the fact that in Figure 2, the lowest strength is shown at the mixing ratio of 50:50, where the number of bond bridges between CBN and aggregate is considered to be the highest. On the other hand, the coefficient of thermal expansion of silicon carbide abrasive grains is 4.2×
Since the thermal expansion coefficient is close to that of CBN at 10 -6 K -1 , the bending strength shows a linear relationship with the mixing ratio without causing any cracks in the bond bridge.
However, since it lacks compatibility with bitrified bond, the strength decreases as the silicon carbide abrasive grains increase. Mullite according to the present invention has a coefficient of thermal expansion of 4.5×
±2.0× with respect to CBN thermal expansion coefficient at 10 -6 K -1
10 -6 K -1 and has good affinity with vitrified bond, so it shows a constant high level of strength regardless of the mixing ratio. In addition, cordierite also exhibits a certain level of strength, similar to mullite. As mentioned above, if the thermal expansion coefficient of the aggregate is ±2.0×10 -6 K -1 relative to the thermal expansion coefficient of CBN, cracks in the bond bridge due to stress between different particles will not occur.
It shows a linear intensity change with respect to concentration. on the other hand,
Compatibility with bitrified bond is good when the aggregate is an oxide such as alumina or mullite, and exhibits high strength. However, the present invention can be applied to particles other than oxides if affinity with the vitrified bond is improved by particle surface treatment or other compounds formed on the particle surfaces. Example 3 Compound CBN#80/100 50 parts by volume Electrofused mullite 50 〃 Vitrified bond * 32 〃 * (Same as Example 1) Thickening agent 20 〃 The particle size of fused mullite is 0.2 of the particle size of CBN, 0.4,
Using particle sizes of 0.6, 0.8, 1.0, 1.2 and double, the compound was press-molded into a disk shape with an outer diameter of 25 mm, a thickness of 14 mm, and a hole diameter of 11 mm, and was fired at 1000°C for 3 hours to obtain a grindstone. . Comparing these whetstones with a whetstone with a concentration of 200,
Figure 3 shows the results of internal grinding. The grinding conditions are as follows. Grinding conditions Grinding wheel peripheral speed 2700m/min Workpiece peripheral speed 75m/min Cutting speed φ1mm/min Oscillation frequency 160cpm Oscillation speed 42m/min Machining allowance φ0.5mm Work material SNCM-420H (HRc42) Work material dimensions Diameter 50 mm x thickness 13 mm x hole diameter 30 mm As is clear from Figure 3, this grindstone with a concentration of 100 is 100% of the grinding wheel with a concentration of 200 when the particle size of the aggregate is 20 to 100% of the particle size of the CBN abrasive grains. Grinding performance of /2 or higher was obtained. In particular, when the aggregate particle size was 60%, a grindstone with a concentration of 100 achieved the same high performance as a grindstone with a concentration of 200. Comparative example 3 Mixed CBN#80/100 50 parts by volume Aggregate 50 〃 Bitrified bond * 32 〃 * (same as Example 1) Sizing material 20 〃 WA #150 and GC #150 were used as aggregates, A grindstone was manufactured in the same manner as in Example 3, and a grinding test was conducted. The results are shown in FIG. Example 4 Compound <CBN#80/100 electrode mullite> 100 parts by weight Vitrified bond 32 〃 Glue 20 〃 The blending amount of CBN was varied to give a concentration of 50, 100, 150, and 200. A grindstone was manufactured in the same manner as in Example 3, and a grinding test was conducted. The results are shown in FIG. As is clear from Figure 4, when a grinding wheel with a concentration of 100 is made using molten alumina or silicon carbide as an aggregate, a grinding ratio of only about 30 to 40% less than that of a grinding wheel with a concentration of 200 can be obtained. When fused mullite was used as the aggregate, the best one had a concentration of 100 and a grinding ratio equivalent to that of a concentration of 200. The performance is higher than that of the straight line). As described above, by selecting the coefficient of thermal expansion, affinity, and particle size of the aggregate, it is possible to fully utilize the characteristics of CBN and provide a higher-performance, lower-cost vitrified CBN grinding wheel. It is. Comparative examples and examples will be shown below regarding the case where diamond abrasive grains are used as superabrasive grains. Comparative example 4
【表】 実施例 5【table】 Example 5
【表】
上記配合物を、CBNの場合と同様に長さ40mm
幅4mm厚味6mmの角柱型にプレス成形し、窒素雰
囲気中、900℃で3時間焼成して砥石とし、3点
曲げ強度を測定した。その結果を第5図に示す。
曲げ強度はダイヤモンド100容量部(集中度200)
の場合を1として相対値で示してある。
第5図から、ホワイトアランダム(WA)を混
合するとCBNの場合と同様に、曲げ強度が低下
する。WAの熱膨張係数は7.4×10-6K-1であつ
て、差±2.0×10-6K-1以内の条件を外れ、従つ
て、このような従来通りの結果となる。
比較例 5
配 合
ダイヤモンド#140/170 50容量部
グリーンカーボランダムGC#230/270
50 〃
ビトリフアイドボンド* 32 〃
糊 料 20 〃
(製造、試験について実施例4に記載)
実施例 6
配 合
ダイヤモンド#140/170 50容量部
電融ムライト#230/270 50容量部
ビトリフアイドボンド* 32 〃
糊 料 20 〃
* 実施例5と同じもの
上記配合物(比較例5、実施例6)を焼結後外
径150mm×厚さ8mm×穴径140mmとなるようリング
状にプレス成形し、窒素雰囲気中900℃で5時間
焼成し、放冷の後仕上後外径140mm×厚さ8mm×
穴径76.2mmの一般(普通)砥石の外周面に接着し
た。これらの砥石を用い下記条件にて平面研削を
行なつた結果を第2表に示す。
研削条件
砥石周速度 1600m/min
クロスフイード 2mm/Pass
テーブル送り速度 10m/min
切込量 0.03mm
被削材 超硬合金K10(HRA90±1)
被削材寸法 長さ50×幅100[Table] The above compound was added to a length of 40 mm as in the case of CBN.
It was press-molded into a prismatic shape with a width of 4 mm and a thickness of 6 mm, and fired at 900° C. for 3 hours in a nitrogen atmosphere to obtain a grindstone, and its three-point bending strength was measured. The results are shown in FIG.
Bending strength is 100 parts by volume of diamond (concentration 200)
It is shown as a relative value with the case of 1 being 1. From Figure 5, when white alundum (WA) is mixed, the bending strength decreases as in the case of CBN. The coefficient of thermal expansion of WA is 7.4×10 −6 K −1 , which is outside the condition of a difference of ±2.0×10 −6 K −1 , and therefore the conventional result is obtained. Comparative Example 5 Compound Diamond #140/170 50 parts by volume Green Carborundum GC #230/270
50 〃 Vitrified bond * 32 〃 Sizing material 20 〃 (Production and testing are described in Example 4) Example 6 Compound diamond #140/170 50 parts by volume Fused mullite #230/270 50 parts by volume Vitrified Bond * 32 〃 Glue 20 〃 * Same as Example 5 After sintering, the above compounds (Comparative Example 5, Example 6) were press-formed into a ring shape with an outer diameter of 150 mm x thickness of 8 mm x hole diameter of 140 mm. Then, baked at 900℃ in a nitrogen atmosphere for 5 hours, left to cool, and finished with an outer diameter of 140 mm x thickness of 8 mm.
It was glued to the outer circumferential surface of a general grindstone with a hole diameter of 76.2 mm. Table 2 shows the results of surface grinding using these grindstones under the following conditions. Grinding conditions Grinding wheel peripheral speed 1600m/min Cross feed 2mm/Pass Table feed speed 10m/min Depth of cut 0.03mm Work material Cemented carbide K10 (HR A 90±1) Work material dimensions Length 50 x Width 100
【表】
第2表から明らかな様に骨材として炭化ケイ素
を用いた砥石に比べ骨材として電融ムライトを用
いた砥石の方が摩耗が少なく1.6倍の性能が得ら
れた。[Table] As is clear from Table 2, the grindstone using fused mullite as an aggregate had less wear and 1.6 times higher performance than the grindstone using silicon carbide as an aggregate.
第1図はCBNと骨材の間に形成されたボンド
ブリツジ及びそのクラツクの模式図である。第2
図は種々の骨材の混合比と曲げ強度との関係を示
す。第3図は骨材(電融ムライト)の粒径比と研
削比(相対値)との関係を示す。第4図は骨材
(電融ムライト)を用いた場合の集中度と研削比
(相対値)との関係及びGC,WAを用いた集中度
100の砥石の研削比(相対値)を示す。第5図は
ダイヤモンド砥粒と骨材の混合比と曲げ強度との
関係を示す。
1…CBN砥粒、2…骨材、3…気孔、4…ク
ラツク、5…ボンド。
Figure 1 is a schematic diagram of the bond bridge and its cracks formed between CBN and aggregate. Second
The figure shows the relationship between the mixing ratio of various aggregates and the bending strength. FIG. 3 shows the relationship between the particle size ratio of the aggregate (electrofused mullite) and the grinding ratio (relative value). Figure 4 shows the relationship between the degree of concentration and grinding ratio (relative value) when using aggregate (electrofused mullite) and the degree of concentration when using GC and WA.
Shows the grinding ratio (relative value) of a grinding wheel of 100. FIG. 5 shows the relationship between the mixing ratio of diamond abrasive grains and aggregate and bending strength. 1... CBN abrasive grain, 2... aggregate, 3... pore, 4... crack, 5... bond.
Claims (1)
を砥粒とするビトリフアイド研削砥石において、
超砥粒の室温〜500℃間の熱膨張係数に対し±2.0
×10-6K-1以内の熱膨張係数を有する酸化物粒子
から成る骨材を砥石中に超砥粒/骨材比90/10〜
10/90容量比配合したことを特徴とする超砥粒砥
石。 2 前記酸化物粒子は1200℃以上の耐火度を有
し、かつ、砥石焼成時にビトリフアイドボンドに
より溶解されないセラミツク粒子である特許請求
の範囲第1項記載の砥石。 3 前記酸化物粒子は超砥粒粒子の20〜100%の
粒径を有する特許請求の範囲第1項又は第2項記
載の砥石。 4 前記酸化物粒子は、溶融ムライト、ジルコ
ン、実質的にムライト結晶から成るアルミナ―シ
リカ系セラミツクス、コーデイエライト又はこれ
らの混合物から成る特許請求の範囲第1項〜第3
項の1に記載の砥石。 5 前記超砥粒は立方晶窒化ホウ素砥粒及び/又
はダイヤモンド砥粒である特許請求の範囲第1項
〜第4項の1に記載の砥石。 6 超砥粒と骨材との合量が砥石中凡そ30〜60容
量%である特許請求の範囲第1項記載の砥石。[Claims] 1. A vitrified grinding wheel using superabrasive grains such as cubic boron nitride and diamond,
±2.0 for the thermal expansion coefficient of superabrasive grains between room temperature and 500℃
Superabrasive grain / aggregate ratio of 90/ 10 ~
A super abrasive grindstone characterized by a 10/90 volume ratio blend. 2. The whetstone according to claim 1, wherein the oxide particles are ceramic particles that have a refractoriness of 1200° C. or higher and are not dissolved by bitrified bond during firing of the whetstone. 3. The grindstone according to claim 1 or 2, wherein the oxide particles have a particle size of 20 to 100% of the superabrasive particles. 4. The oxide particles are comprised of molten mullite, zircon, alumina-silica ceramics consisting essentially of mullite crystals, cordierite, or a mixture thereof.
The whetstone described in item 1. 5. The grindstone according to claim 1, wherein the superabrasive grains are cubic boron nitride abrasive grains and/or diamond abrasive grains. 6. The whetstone according to claim 1, wherein the total amount of superabrasive grains and aggregate in the whetstone is approximately 30 to 60% by volume.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56180991A JPS5882677A (en) | 1981-11-13 | 1981-11-13 | Super particle grindstone |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56180991A JPS5882677A (en) | 1981-11-13 | 1981-11-13 | Super particle grindstone |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5882677A JPS5882677A (en) | 1983-05-18 |
| JPH0138628B2 true JPH0138628B2 (en) | 1989-08-15 |
Family
ID=16092821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56180991A Granted JPS5882677A (en) | 1981-11-13 | 1981-11-13 | Super particle grindstone |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5882677A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2042268A2 (en) | 2007-09-28 | 2009-04-01 | Toyoda Van Moppes Ltd. | Grinding wheel |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4657563A (en) * | 1985-10-31 | 1987-04-14 | Norton Company | Resin bonded grinding wheels with fillers |
| JPH0669669B2 (en) * | 1985-12-20 | 1994-09-07 | 日本精工株式会社 | Super Abrasive Grain |
| JPH0716881B2 (en) * | 1988-06-16 | 1995-03-01 | 株式会社ノリタケカンパニーリミテド | Vitrified superabrasive stone |
| JP2554425Y2 (en) * | 1989-03-28 | 1997-11-17 | 三菱マテリアル株式会社 | Inner circumference grinding wheel |
| JP2699202B2 (en) * | 1989-07-19 | 1998-01-19 | 旭ダイヤモンド工業株式会社 | Cleaning wheel for TAB bonding tool |
| JP4562609B2 (en) * | 2005-07-28 | 2010-10-13 | 本田技研工業株式会社 | Vitrified grinding wheel, method of manufacturing the same, and cast iron workpiece grinding method using the same |
| WO2008062846A1 (en) * | 2006-11-22 | 2008-05-29 | Asahi Glass Company, Limited | Dressing stone, glass composition for holding abrasive grains, and glass-ceramic composition for holding abrasive grains |
| JP5192763B2 (en) * | 2007-09-18 | 2013-05-08 | 株式会社ノリタケカンパニーリミテド | Method for producing superabrasive vitrified grinding wheel |
| CN111942330B (en) * | 2019-05-17 | 2021-12-14 | 常州中车铁马科技实业有限公司 | A kind of modification grinder and its making method |
-
1981
- 1981-11-13 JP JP56180991A patent/JPS5882677A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2042268A2 (en) | 2007-09-28 | 2009-04-01 | Toyoda Van Moppes Ltd. | Grinding wheel |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5882677A (en) | 1983-05-18 |
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