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JPH0428502B2 - - Google Patents
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JPH0428502B2 - - Google Patents

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Publication number
JPH0428502B2
JPH0428502B2 JP58035174A JP3517483A JPH0428502B2 JP H0428502 B2 JPH0428502 B2 JP H0428502B2 JP 58035174 A JP58035174 A JP 58035174A JP 3517483 A JP3517483 A JP 3517483A JP H0428502 B2 JPH0428502 B2 JP H0428502B2
Authority
JP
Japan
Prior art keywords
grinding
grindstone
abrasive grains
grinding wheel
cbn
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 - Lifetime
Application number
JP58035174A
Other languages
Japanese (ja)
Other versions
JPS59161269A (en
Inventor
Noboru Matsumori
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mizuho Co Ltd
Original Assignee
Mizuho Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mizuho Co Ltd filed Critical Mizuho Co Ltd
Priority to JP3517483A priority Critical patent/JPS59161269A/en
Publication of JPS59161269A publication Critical patent/JPS59161269A/en
Publication of JPH0428502B2 publication Critical patent/JPH0428502B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02Physical 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
    • B24D3/04Physical 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
    • B24D3/14Physical 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
    • B24D3/18Physical 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 for porous or cellular structure

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Polishing Bodies And Polishing Tools (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は、磁器質結合剤、すなわちビトリフ
アイドを使用した多孔性ビトリフアイド窒化硼素
砥石の製造方法に関する。 従来、小径砥石による内面研削加工などを行な
うには、この発明の出願人が既に特公昭57−
49351号で提案したような通常組織を有し、砥石
直径が約15mm以下のビトリフアイド窒化硼素砥石
を用いて、満足な研削加工ができる。しかし、砥
石直径が25mmを越えるような大径砥石による通し
孔の研削もしくは円弧溝面の内面研削、または、
等速ボールジヨイントの外輪溝研削等の際には、
砥石と工作物との接触弧もしくは接触面が増大す
るので、目詰まりを生じやすい。また砥石の硬度
を上げて、その砥石摩耗が僅少で経済的な研削加
工を行なおうとすれば、砥石表面に金属屑の溶着
などがみられるようになり、研削に適当な面が得
られない。一方、従来のアルミナ質や炭化珪素質
などの一般砥粒を使用した多孔性砥石は、炭素工
具鋼、高速度鋼、合金工具鋼等の工具用鋼、また
は、アルミニウム合金、焼結合金等の難削材を対
象として、砥石結合度もアルフアベツト硬度
(JIS−R6210−1980)で、硬くしてもJ以下と軟
位砥石を使用し、砥石摩耗を犠性にして研削性に
重点を置いたものであり、研削比も5%以下と小
さい。したがつて、高価な立方晶窒化硼素砥粒
(以下これをCBN砥粒と略称する)を使用して、
従来技術により多孔性砥石を作製しようものな
ら、直ちに経済的な研削加工は不可能になり、有
用性は全く失われてしまうのである。 なお、ビトリフアイドCBN砥石は、約1000℃
以上の高温で砥粒が変質しやすいこと、もしく
は、砥粒の膨張係数が3.5×10-6cm/cm/℃と低
い値であることから、これに適合して結合力にす
ぐれたボンドを選択するには限界があるなどの諸
問題がある。このような問題を克服するために、
前記特公昭57−49351号のように、レジノイドボ
ンドCBN砥石と比較して、結合剤が砥粒支持力
にすぐれ、剛性があり、しかも、砥石組織がより
多孔質であるようなビトリフアイドCBN砥石が
開発され、このような砥石が精密研削分野で広く
利用される方向にある。 しかし、これらビトリフアイドCBN砥石の特
徴を助長し、かつ砥石摩耗量をさらに少なくする
ために、結合剤量の増量調整等によつて高度の経
済性を求めようとすれば、砥石は激しく目詰まり
を生じ、ドレツシング頻度を増し、ドレツシング
による砥石消耗およびドレツサーの摩耗等が著し
く増大して、ある限度以上に高い経済性を追求す
ることができないのが実情である。特にこのよう
な現象は、砥石と工作物との接触弧もしくは接触
面の大きい研削加工、または、工具用鋼などの難
削材の研削の際に顕著である。他方、砥石摩耗が
増大することなく、砥石目詰まりを改善して、研
削中に砥粒先端の研削点付近において自動的に空
隙を生ぜしめ、研削屑の排出を容易にし、研削性
高めようとする手段が試みられている。その中に
は、たとえば、つぎのようなものがある。すなわ
ち、 ガラス質もしくはセラミツク質CBN砥石に
おいて、アルミナ質砥粒よりも軟らかく摩耗し
やすく、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ジルコンまたはムライ
ト等の骨材を使用する砥石(特公昭52−27394
号)。 有機質または無機質の微小中空体が研削中の
砥石のチツプポケツトである気孔として作用す
る熱硬化性樹脂を結合材とする微粒砥石(特開
昭55−137887号)。 液体潤滑剤もしくは冷却剤を使用しない超硬
工具および高速度鋼等の乾式研削で、研削抵抗
が低く研削比の大きい性能を目的として、セラ
ミツクマトリツクスに対して黒鉛、六方晶窒化
硼素および二硫化モリブデン等を適当量だけ存
在させたダイヤモンドもしくはCBN砥石(特
公昭49−5717号)。 などである。ここで、これらの砥石は、いずれも
研削の際の研削点における研削抵抗を下げ、クー
ルグラインデイングに大きく貢献すると考えられ
るチツプポケツトの形成のため、または、潤滑性
付与のための有効な成分を含有している点で共通
しているが、砥石摩耗が少なくて高度に経済的な
研削加工が遂行できるかどうかについては未だ満
足できる段階には至つていない。 この発明は、上記した現状に着目し、僅少な砥
石摩耗量の下で高能率研削を行なつても目詰まり
を起こしにくく、クールグラインデイングが可能
で、ドレツシング(目直し)が容易であり、しか
もドレツサー(目直し工具)の摩耗も改善され
て、砥石寿命が著しく延び、経済的研削加工が達
成し得る砥石の製造方法を提供することを目的と
している。 上記目的を達成するために、この発明において
は、CBN砥粒をビトリフアイドボンドで結合し
た砥石の製造方法において、砥粒径の2〜4倍の
粒子径を有し比重が1.0〜1.4付近で24時間当たり
の吸水率0.1%以下の有機性粒子を砥粒100重量部
に対し、3〜12重量部配合し、加圧成形して乾燥
した後焼成したものである。以下にその詳細を述
べる。 まず、この発明において使用するCBN砥粒の
粒度は、特に限定するものではないが、実用面で
の研削性、表面粗度および後述する有機性粒子の
大きさ等から、80/100〜270/325メツシユ
(ANSI全米規格協会)のものを適宜選べばよい。 つぎに、この発明の有機性粒子とは、砥石焼成
中に焼失し、砥石の組織に気孔を形成させるため
のものであり、少量(重量)の使用で大きい効果
の得られるもの、すなわち比重が1.0〜1.4付近
で、砥石成形時の加圧もしくは吸湿等による体積
変化の少ないもの、すなわち弾力性は小さく(た
とえば弾性率200〜300Kgf/mm2)吸水率(24時
間)0.1%以下で、さらに、焼成時有毒ガスを発
生しないものが望ましく、合成樹脂たとえばスチ
ロール樹脂、ポリエステル樹脂、変性ポリフエニ
レンオキシド、エポキシ樹脂などを例示すること
ができる。なお、一般に構造的に極性基をもつて
いるプラスチツクは、吸水率が大きく、したがつ
て吸水に伴う弾性率の低下も大きく不適当であ
る。また、比重が小さい点では木質材も例外では
ないが、弾力性および吸水性が大きく、圧縮成形
後に亀裂を生ずる原因となるため好ましくない。
しかし、このような木質材であつても、樹脂加工
等によつてこれら問題となる性質を改善すれば、
充分使用に耐える材料となりうる。 このような有機性粒子の大きさは、使用する砥
粒の大きさの2〜4倍とし、添加量は砥粒100重
量部に対して3〜12重量部であることが望まし
い。なぜならば、砥粒径よりも大きい有機性粒子
を使用して砥石を作るとき、前記の条件範囲外の
粒子および配合割合のものは、焼成時の収縮が大
きく、焼成中に変形もしくは亀裂を生じ製造上困
難な問題が生ずるばかりではなく、製品の強度も
低く、回転操業時の安全性にも支障を来たすから
である。そして、砥粒径よりも大きい有機性粒子
は、砥石焼成前の状態では骨材の役割を果たすも
のであるから、他の材料と混合攪拌するときにお
いても容易に変形したり、摩耗したりすることな
く、また、粒子の形状も、砥石組織を均質なもの
とするために、球状、楕球状、顆粒状もしくはこ
れに類する形状で、長径と短径または径と高さの
比が1に近い値、たとえば1〜1.2、であること
が好ましい。 以上述べたCBN砥粒および有機性粒子に、ビ
トリフアイドボンドならびに成形のための粘結材
(たとえば、デキストリンの粉末もしくは水溶液)
を充分に攪拌混合し、任意の砥石形状に加圧成形
して乾燥した後、これを窒化雰囲気下1200〜1300
℃で約1.5〜2.0時間焼成する。ここで窒素雰囲気
下で焼成する理由は、CBN砥粒が約800℃以上の
高温付近から徐々に酸化しはじめて、さらに1000
℃以上の高温で酸化硼素となつてCBN砥粒本来
の高度を喪失しないようにするためである。した
がつて、砥石中に含有されている有機性粒子は、
微酸化もしくは中性雰囲気とした約400〜600℃付
近の温度下において、砥粒とボンドとの結合力に
影響を及ぼすことなく完全に焼失することが必要
であり、また、ビトリフアイドボンドは1200〜
1300℃の高温下で融化が充分に進行し、充分に満
足できる結合力を生ずるものでなければならない
ことは言うまでもない。 このような多孔性ビトリフアイドCBN砥石の
製造方法によると、ビトリフアイドボンドに砥粒
と共に分散保持された有機性粒子の吸水率が低
く、このため、膨潤による体積増加や弾力性の低
下の割合がきわめて小さく、かつその比重も効率
的な分散に好ましいものであるため、加圧成形す
る時、有機性粒子が均等に分散した状態で配合当
初の粒径を維持する。 加圧成形後においては、成形物内部から余分の
水分、空気等が排除された高密度下で前記の有機
性粒子が一層均等に分布することになり、ついで
このような理想的な有機性粒子の分散状態が維持
された状態で乾燥および焼成がなされる。また、
焼成時に焼失する有機性粒子は、低吸水性である
ことから水分を周囲に放出することがなく、この
ため、気孔から急速に水蒸気が輝散して気孔周辺
にひびび割れが生ずる不都合がない。 本願発明は、このようにして形成された単位気
孔そのものがチツプポケツトとして目詰まりを起
こしにくくし、低研削抵抗で研削性にすぐれると
同時に、砥石(砥粒)摩耗がきわめて少ないの
で、従来品にはその類を見ない高度の経済性のあ
る砥石が得られる。 以下に実施例を示す。 〔実施例〕 140/170メツシユのCBN砥粒に対して、スチ
ロール樹脂粒の大きさが、JIS−Z8801−1966に
定められた標準篩の呼び寸法に基づいて、約2倍
(210μ篩を通過して177μ篩上に留るもので、
177/210と略記する。以下同様)、約3倍(297/
350)および約4倍(420/500)である群を選び、
第1表に示すように粒子の大きさおよび混合量
(CBN砥粒100重量部に対する重量部)の異なる
5種類の試料砥石と、スチロール樹脂粒を含まな
い対照品1種類とを調製した。試料砥石は所定料
のCBN砥粒、スチロール樹脂粒、ビトリフアイ
ドボンドおよびデキストリンをよく攪拌混合し、
焼成後の砥石で、砥粒、ボンドおよび気孔の体積
を、砥石の体積で除いた値(%)が、それぞれ砥
粒率37.5、ボンド率25.0および気孔率37.5となる
ような生砥石の嵩比重を予め計算で求めておき、
この嵩比重をもとにして各配合割合およば成形圧
力を定めて、外径25mm、内径10mm、高さ30mmの生
砥石を成形した。成形後、これらの生砥石を乾燥
した後、窒素ガス雰囲気下にある電気炉によつ
て、品温が加熱時600℃から最高温度1250℃に保
持され、冷却時600℃に降下するまでの所要時間
が48時間となるような条件で焼成し、得られた砥
石についてRM硬度、研削比および研削サイクル
等の測定を行ない、それらの結果を第1表
The present invention relates to a method of manufacturing a porous vitrified boron nitride grinding wheel using a porcelain binder, vitrified. Conventionally, in order to perform internal grinding using a small-diameter grindstone, the applicant of this invention has already developed
Satisfactory grinding can be achieved using a vitrified boron nitride grindstone with a normal structure as proposed in No. 49351 and a grindstone diameter of approximately 15 mm or less. However, grinding of through holes or internal grinding of arcuate groove surfaces with a large-diameter grindstone with a grindstone diameter exceeding 25 mm, or
When grinding the outer ring groove of a constant velocity ball joint, etc.
Since the contact arc or contact surface between the grindstone and the workpiece increases, clogging is likely to occur. Furthermore, if we try to increase the hardness of the grinding wheel and perform economical grinding with minimal wear on the grinding wheel, welding of metal chips will occur on the surface of the grinding wheel, making it impossible to obtain a suitable surface for grinding. . On the other hand, conventional porous grinding wheels that use general abrasive grains such as alumina and silicon carbide are made of tool steels such as carbon tool steel, high-speed steel, and alloy tool steel, or of tool steels such as aluminum alloys and sintered alloys. Targeting difficult-to-cut materials, we used a soft grindstone with an alpha-average hardness (JIS-R6210-1980) and less than J even when hardened, placing emphasis on grindability at the expense of grinding wheel wear. The grinding ratio is also small at less than 5%. Therefore, using expensive cubic boron nitride abrasive grains (hereinafter referred to as CBN abrasive grains),
If a porous grinding wheel were to be produced using conventional techniques, economical grinding would soon become impossible and its usefulness would be completely lost. In addition, the Vitrified CBN grinding wheel has a temperature of approximately 1000℃.
Because the abrasive grains tend to deteriorate at higher temperatures, or because the coefficient of expansion of the abrasive grains is as low as 3.5×10 -6 cm/cm/°C, a bond with excellent bonding strength that is compatible with this is used. There are various problems, such as the fact that there are limits to the choices that can be made. In order to overcome such problems,
As described in the above-mentioned Japanese Patent Publication No. 57-49351, a vitrified CBN grinding wheel has a binder that has excellent abrasive grain support, is more rigid, and has a more porous structure than a resinoid bonded CBN grinding wheel. This type of grinding wheel has been developed and is on the way to being widely used in the precision grinding field. However, in order to promote these characteristics of the vitrified CBN grinding wheel and further reduce the wear amount of the grinding wheel, if we try to achieve high economic efficiency by increasing the amount of binder, etc., the grinding wheel will become severely clogged. The reality is that the frequency of dressing increases, and the wear of the grindstone and wear of the dresser due to dressing increases significantly, making it impossible to pursue higher economic efficiency beyond a certain limit. This phenomenon is particularly noticeable when grinding a grindstone with a large contact arc or contact surface between the grindstone and the workpiece, or when grinding difficult-to-cut materials such as tool steel. On the other hand, we are trying to improve grinding performance by improving grinding wheel clogging without increasing grinding wheel wear, automatically creating a void near the grinding point at the tip of the abrasive grain during grinding, and facilitating the discharge of grinding debris. Measures are being tried to do so. Among them are the following, for example: In other words, a vitreous or ceramic CBN grinding wheel that uses an aggregate such as zircon or mullite, which is softer and more abrasive than alumina abrasive grains and whose main component is crystals with a modified Mohs hardness of 11 or less and a melting point of 900°C or more. (Tokuko Showa 52-27394
issue). A fine-grained grindstone in which organic or inorganic micro hollow bodies act as pores, which are chip pockets of the grinding wheel, as a binder (Japanese Patent Laid-Open No. 137887/1987). Graphite, hexagonal boron nitride, and disulfide are added to ceramic matrices for the purpose of low grinding resistance and high grinding ratio performance in dry grinding of cemented carbide tools and high-speed steel without using liquid lubricants or coolants. A diamond or CBN whetstone containing an appropriate amount of molybdenum, etc. (Special Publication No. 5717, 1973). etc. All of these grindstones contain effective ingredients to reduce the grinding resistance at the grinding point during grinding and to form chip pockets, which are thought to greatly contribute to cool grinding, or to provide lubricity. However, we have not yet reached a satisfactory stage as to whether highly economical grinding can be performed with less wear on the grinding wheel. Focusing on the above-mentioned current situation, this invention has been developed to provide a system that is difficult to clog even when performing high-efficiency grinding with a small amount of grindstone wear, allows cool grinding, and is easy to dress (reface). Furthermore, it is an object of the present invention to provide a method for manufacturing a grindstone that can improve the wear of the dresser (redressing tool), significantly extend the life of the grindstone, and achieve economical grinding. In order to achieve the above object, the present invention provides a method for manufacturing a grinding wheel in which CBN abrasive grains are bonded with a vitrified bond, the particle size is 2 to 4 times the abrasive grain size, and the specific gravity is around 1.0 to 1.4. 3 to 12 parts by weight of organic particles having a water absorption rate of 0.1% or less per 24 hours are mixed with 100 parts by weight of abrasive grains, pressure molded, dried, and then fired. The details are described below. First, the particle size of the CBN abrasive grains used in this invention is not particularly limited, but is determined from 80/100 to 270/ 325 (ANSI National Standards Institute) as appropriate. Next, the organic particles of this invention are those that are burned away during grindstone firing and form pores in the structure of the grindstone, and are those that can achieve a large effect with a small amount (weight) of use, that is, those that have a specific gravity. 1.0 to 1.4, with little volume change due to pressure or moisture absorption during grindstone forming, that is, elasticity is small (for example, elastic modulus 200 to 300 Kgf/mm 2 ), water absorption rate (24 hours) is 0.1% or less, and It is desirable to use a material that does not generate toxic gas during firing, and examples thereof include synthetic resins such as styrene resin, polyester resin, modified polyphenylene oxide, and epoxy resin. In general, plastics having a polar group in their structure have a large water absorption rate, and therefore the elastic modulus decreases greatly due to water absorption, making them unsuitable. Furthermore, although wood materials are no exception in that they have a low specific gravity, they are undesirable because they have high elasticity and water absorption, which can cause cracks to occur after compression molding.
However, even with such wood materials, if these problematic properties are improved through resin processing, etc.
It can be a material that is durable enough to withstand use. The size of such organic particles is preferably 2 to 4 times the size of the abrasive grains used, and the amount added is preferably 3 to 12 parts by weight per 100 parts by weight of the abrasive grains. This is because when making a whetstone using organic particles that are larger than the abrasive grain size, particles and blending ratios that are outside the above conditions will shrink significantly during firing and may deform or crack during firing. This is because not only difficult problems arise in manufacturing, but also the strength of the product is low, which impedes safety during rotational operation. Organic particles larger than the abrasive grain size play the role of aggregate before firing the whetstone, so they are easily deformed or worn out when mixed with other materials. In addition, in order to make the grinding wheel structure homogeneous, the shape of the particles is spherical, ellipsoidal, granular, or similar, and the ratio of the major axis to the minor axis or the diameter to the height is close to 1. A value of, for example, 1 to 1.2 is preferred. In addition to the CBN abrasive grains and organic particles described above, vitrified bond and a binding agent for molding (for example, dextrin powder or aqueous solution)
After thoroughly stirring and mixing, press-forming into any desired shape and drying, it is heated to 1200 to 1300 in a nitriding atmosphere.
Bake for approximately 1.5-2.0 hours at °C. The reason for firing in a nitrogen atmosphere is that CBN abrasive grains begin to oxidize gradually at a high temperature of approximately 800°C or higher, and then
This is to prevent CBN abrasive grains from losing their original height due to becoming boron oxide at high temperatures above ℃. Therefore, the organic particles contained in the grindstone are
It is necessary to completely burn out without affecting the bonding force between the abrasive grains and the bond at a temperature of around 400 to 600℃ in a slightly oxidized or neutral atmosphere. 1200〜
It goes without saying that melting must proceed sufficiently at a high temperature of 1300° C. and a sufficiently satisfactory bonding force must be produced. According to the manufacturing method of such a porous vitrified CBN grindstone, the water absorption rate of the organic particles dispersed and held together with the abrasive grains in the vitrified bond is low, and therefore the rate of increase in volume and decrease in elasticity due to swelling is low. Since it is extremely small and its specific gravity is favorable for efficient dispersion, during pressure molding, the organic particles are uniformly dispersed and maintain the particle size at the time of blending. After pressure molding, the above-mentioned organic particles are more evenly distributed under a high density environment in which excess moisture, air, etc. are removed from the inside of the molded product, and then these ideal organic particles are Drying and firing are performed while maintaining the dispersed state of the particles. Also,
The organic particles that are burnt away during firing have low water absorption and do not release moisture into the surrounding area.Therefore, there is no problem of water vapor rapidly dissipating from the pores and causing cracks around the pores. . In the present invention, the unit pores themselves formed in this way act as chip pockets to prevent clogging, and have low grinding resistance and excellent grinding performance. At the same time, the wear of the grinding wheel (abrasive grains) is extremely low, so it is better than conventional products. You can obtain a highly economical whetstone like no other. Examples are shown below. [Example] Compared to 140/170 mesh CBN abrasive grains, the size of the styrene resin particles is approximately twice that of the standard sieve size specified in JIS-Z8801-1966 (passing through a 210μ sieve). and remains on the 177μ sieve.
Abbreviated as 177/210. (same below), approximately 3 times (297/
350) and about 4 times (420/500),
As shown in Table 1, five types of sample grindstones with different particle sizes and mixed amounts (parts by weight relative to 100 parts by weight of CBN abrasive grains) and one control product containing no styrene resin particles were prepared. The sample grindstone is made by thoroughly stirring and mixing the specified materials of CBN abrasive grains, styrene resin grains, vitrified bond, and dextrin.
Bulk specific gravity of a raw whetstone after firing, such that the values (%) obtained by subtracting the volumes of abrasive grains, bonds, and pores by the volume of the whetstone are abrasive grain ratio of 37.5, bond ratio of 25.0, and porosity of 37.5, respectively. Calculate in advance,
Based on this bulk specific gravity, each compounding ratio and molding pressure were determined, and a green grindstone with an outer diameter of 25 mm, an inner diameter of 10 mm, and a height of 30 mm was molded. After forming and drying these green grindstones, the product temperature is maintained from 600℃ during heating to a maximum temperature of 1250℃ using an electric furnace under a nitrogen gas atmosphere, and the time required for it to drop to 600℃ during cooling. The grinding wheel was fired under conditions such that the grinding time was 48 hours, and the RM hardness, grinding ratio, grinding cycle, etc. were measured, and the results are shown in Table 1.

【表】 に併記した。なお、各測定方法はつぎのとおりで
ある。すなわち、 RM硬度: ロツクウエル硬度計において、直径1/4イン
チの鋼球を使用し、荷重は100Kgとする。 研削比および研削サイクル: 東洋工業製の内面研削盤で、水溶性研削油
(50倍稀釈液)を使用して、軸受鋼(SUJ2種、
ロツクウエル硬度Cスケールで60/62)の内面
(内径35mm、幅25mm)を研削する。この際の主
は研削条件は、砥石回転数を毎分29000回、工
作物回転数を毎分770回とし、テーブルオシレ
ート量20mm、オシレート回数毎分100サイクル
で、フロントフオークゲージング装置で直接加
工内径の変化を測定しながら定圧切込みで研削
を行なつた。したがつて、前加工寸法で研削代
が直径で0.16mmとなるように取揃えた加工物で
試料砥石の研削性能の差によつて研削サイクル
(秒)が変化し、研削性にすぐれる砥石では、
研削サイクルは短くなり、反対に研削性で劣る
ときは長時間を必要とする。一方、ドレツシン
グは、ダイヤモンドドレツサーによつて砥石研
削面の条件を一定にした。以上のような研削条
件でドレツシングした後、各砥石について、加
工物30個を連続して研削試験を行ない、研削除
去された被削材の累積体積(mm3)を研削量と
して、この研削量を砥石摩耗量(mm3)で除し
た値を削比とする。 である。 第1表に示したとおり、スチロール樹脂粒の大
きさがCBN砥粒の大きさの約2倍と小さく、添
加量も5%と少ない試料1−1の砥石において
は、研削比は高くなるが、研削性において劣り、
研削サイクルは長くなつている。逆に試料3−2
のように大きさが約4倍と大きく、添加量も11%
と多いスチロール樹脂粒を用いたものは、研削比
は低くなるが研削サイクルは大幅に短縮されてい
る。要するに、スチロール樹脂粒の大きさは
CBN砥粒の2〜4倍においても最も望ましい結
果が得られ、2倍未満の小粒子の樹脂粒を添加量
5%未満の少量としたときは、第1表に示す対照
砥石の性能に近似して研削比は大きくなるが、研
削性は劣り、研削サイクルは長くなつて、添加効
果は顕著でない。それに対して、4倍を越える大
粒子の樹脂粒を添加量11%よりも多くしたとき
は、研削性は向上し、研削サイクルは短縮する
が、砥石摩耗量は増加して、研削比は低くなり好
ましいものとは言えないことが明らかとなつた。 この発明は、以上説明したように、所定の粒子
径、比重、吸水率の有機性粒子を所定の配合割合
で砥粒に添加し、焼成することによつて、ビトリ
フアイドCBN砥石内に均等に分布する均質のチ
ツプポケツトを形成することができ、製造された
砥石は僅少な砥石摩耗量の下で高能率かつ精密な
研削を行ない得て、しかも目詰まりを起こしにく
い。したがつて、ドレツシングの頻度が少なくて
長寿命であり、経済的研削加工を達成し得てクー
ルグライデイングも可能な高性能の多孔性ビトリ
フアイドCBN砥石を製造でき、この発明の産業
上の利用価値は高いということができる。
It is also listed in [Table]. In addition, each measurement method is as follows. That is, RM hardness: A steel ball with a diameter of 1/4 inch is used on the Rockwell hardness tester, and the load is 100 kg. Grinding ratio and grinding cycle: Bearing steel (SUJ2 type,
Grind the inner surface (inner diameter 35 mm, width 25 mm) of 60/62 on the Rockwell hardness C scale. The main grinding conditions in this case were a grinding wheel rotation speed of 29,000 times per minute, a workpiece rotation speed of 770 times per minute, a table oscillation amount of 20 mm, an oscillation frequency of 100 cycles per minute, and a front fork gauging device that directly machined the inner diameter. Grinding was carried out at a constant cutting pressure while measuring the change in . Therefore, the grinding cycle (seconds) will change depending on the difference in the grinding performance of the sample grindstone for a workpiece prepared so that the grinding allowance is 0.16 mm in diameter in the pre-processing dimensions, and the grinding cycle (seconds) will change depending on the difference in the grinding performance of the sample grindstone. ,
The grinding cycle becomes shorter, and on the other hand, when the grindability is poor, a long time is required. On the other hand, for dressing, the conditions of the grinding surface of the grindstone were kept constant using a diamond dresser. After dressing under the above grinding conditions, a grinding test was performed on 30 workpieces in succession for each grinding wheel, and the amount of grinding was calculated using the cumulative volume (mm 3 ) of the workpiece removed by grinding. The value obtained by dividing the amount by the grinding wheel wear amount (mm 3 ) is the cutting ratio. It is. As shown in Table 1, in the grinding wheel of sample 1-1, the size of the styrene resin grains is small, about twice the size of the CBN abrasive grains, and the amount added is small at 5%, although the grinding ratio is high. , inferior in grindability,
Grinding cycles are getting longer. On the contrary, sample 3-2
The size is about 4 times larger, and the amount added is 11%.
Products that use a large number of styrene resin particles have a lower grinding ratio, but the grinding cycle is significantly shorter. In short, the size of the styrene resin particles is
The most desirable results were obtained even with 2 to 4 times the CBN abrasive grains, and when a small amount of resin grains less than 2 times the size was added, less than 5%, the performance approximated that of the control wheel shown in Table 1. Although the grinding ratio increases, the grindability is poor, the grinding cycle becomes longer, and the effect of addition is not significant. On the other hand, when adding more than 11% of the resin grains, which are more than 4 times larger, the grindability improves and the grinding cycle is shortened, but the amount of grinding wheel wear increases and the grinding ratio becomes low. It became clear that this was not a desirable result. As explained above, this invention adds organic particles with a predetermined particle size, specific gravity, and water absorption rate to abrasive grains at a predetermined blending ratio, and by firing the organic particles, the organic particles are evenly distributed within a vitrified CBN grindstone. The manufactured grindstone can perform highly efficient and precise grinding with a small amount of grindstone wear, and is less prone to clogging. Therefore, it is possible to produce a high-performance porous bitrified CBN grinding wheel that requires less dressing, has a long life, can achieve economical grinding, and is also capable of cool gliding, and this invention has industrial utility value. can be said to be high.

Claims (1)

【特許請求の範囲】[Claims] 1 立方晶窒化硼素砥粒をビトリフアイドボンド
で結合する砥石の製造方法において、砥粒径の2
〜4倍の粒子径を有し比重が1.0〜1.4付近で24時
間当たりの吸水率0.1%以下の有機性粒子を、砥
粒100重量部に対し3〜12重量部配合し、加圧成
形して乾燥した後焼成することを特徴とする多孔
性ビトリフアイド窒化硼素砥石の製造方法。
1 In a method for manufacturing a grinding wheel that combines cubic boron nitride abrasive grains with a vitrified bond,
3 to 12 parts by weight of organic particles with a particle diameter of ~4 times as large, a specific gravity of around 1.0 to 1.4, and a water absorption rate of 0.1% or less per 24 hours are mixed with 100 parts by weight of abrasive grains, and then pressure molded. A method for producing a porous vitrified boron nitride grindstone, which comprises drying the grindstone and then firing it.
JP3517483A 1983-03-03 1983-03-03 Porous vitrified boron nitrified grindstone Granted JPS59161269A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3517483A JPS59161269A (en) 1983-03-03 1983-03-03 Porous vitrified boron nitrified grindstone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3517483A JPS59161269A (en) 1983-03-03 1983-03-03 Porous vitrified boron nitrified grindstone

Publications (2)

Publication Number Publication Date
JPS59161269A JPS59161269A (en) 1984-09-12
JPH0428502B2 true JPH0428502B2 (en) 1992-05-14

Family

ID=12434485

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3517483A Granted JPS59161269A (en) 1983-03-03 1983-03-03 Porous vitrified boron nitrified grindstone

Country Status (1)

Country Link
JP (1) JPS59161269A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2700800B2 (en) * 1988-07-19 1998-01-21 株式会社佐竹製作所 Method for producing porous grindstone for rice polishing and porous grindstone for rice polishing
JPH03184771A (en) * 1989-12-13 1991-08-12 Kurenooton Kk Porous vitrified grinding wheel and manufacture thereof
US5536282A (en) * 1994-11-08 1996-07-16 Cincinnati Milacron Inc. Method for producing an improved vitreous bonded abrasive article and the article produced thereby
EP1634678A4 (en) * 2003-05-30 2007-05-30 Bosch Corp Vitrified grinding wheel and method of manufacturing the same

Also Published As

Publication number Publication date
JPS59161269A (en) 1984-09-12

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