JPH02269567A - Manufacture of vitrified grinding wheel - Google Patents

Manufacture of vitrified grinding wheel

Info

Publication number
JPH02269567A
JPH02269567A JP8782289A JP8782289A JPH02269567A JP H02269567 A JPH02269567 A JP H02269567A JP 8782289 A JP8782289 A JP 8782289A JP 8782289 A JP8782289 A JP 8782289A JP H02269567 A JPH02269567 A JP H02269567A
Authority
JP
Japan
Prior art keywords
abrasive grains
grinding
vitrified
particles
firing
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
Application number
JP8782289A
Other languages
Japanese (ja)
Inventor
Hikari Hasegawa
光 長谷川
Tadashi Hiraiwa
正 平岩
Kiyoshi Katayama
片山 清
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.)
Resonac Holdings Corp
Original Assignee
Showa Denko KK
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 Showa Denko KK filed Critical Showa Denko KK
Priority to JP8782289A priority Critical patent/JPH02269567A/en
Publication of JPH02269567A publication Critical patent/JPH02269567A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To use vitrified bond without limitations so as to obtain a grinding wheel of high hardness by mixing non-burned grinding particles with vitrified bond and molding them, and performing burning of the grinding particles simultaneously with that of the grinding wheel. CONSTITUTION:Particles heated to temperatures from above 100 deg.C to below 1,250 deg.C within 120 seconds and held within 90 seconds for a rapid-heating treatment are used as non-burned grinding particles. These non-burned grinding particles are mixed with vitrified bond and molded, and burning of the grinding particles is carried out simultaneously with that of grinding stone. Loss of energy and growing of crystals are thereby restrained, and a vitrified grinding wheel of excellent grinding performance is obtained.

Description

【発明の詳細な説明】 〔産業上の利用分野] 本発明は工具鋼等の精密研削に用いるためのアルミナ質
焼結砥粒を含むビトリファイド砥石の製造方法に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for producing a vitrified grindstone containing alumina sintered abrasive grains for use in precision grinding of tool steel and the like.

[従来の技術] 砥粒には電融等によってつくられる原料塊を粉砕分級し
て作られる、いわゆる単結晶に近い砥粒と多(の微結晶
から構成される多結晶砥粒がある。
[Prior Art] Abrasive grains include polycrystalline abrasive grains, which are made by crushing and classifying raw material lumps produced by electrofusion, etc., and are composed of so-called single-crystal abrasive grains and polycrystalline microcrystals.

多結晶砥粒には、バインダー等で練られた原料粉を成形
し、焼成炉で焼結させる方法や、ゾルゲル法から出発す
る方法がある。ゾルゲル法の場合、焼成前の状態として
乾燥ゲルを使用する場合や、これを仮焼して水をとばし
たものがある。
Polycrystalline abrasive grains can be produced by forming raw material powder kneaded with a binder or the like and sintering it in a kiln, or by starting from a sol-gel method. In the case of the sol-gel method, there are cases where a dry gel is used as a state before firing, and cases where this is calcined to remove water.

又、いわゆる単結晶砥粒の中にも焼成(ロースト)工程
を経て砥粒として完成するものがある。
Furthermore, some so-called single crystal abrasive grains are completed as abrasive grains through a baking (roasting) process.

従来、サブミクロンの微結晶のアルミナ質焼結砥粒から
成るすぐれた研削性能を有するビトリファイド研削砥石
をつくるためには、例えば特開昭61−56872号に
記載されている如(、まずアルミナゲル粒子を1250
〜1400℃に仮焼してaAβ203の微結晶よりなる
砥粒(ルース・グレン)を作り、これにビトリファイド
結合剤を加えて約1220℃で焼成することが必要であ
った。
Conventionally, in order to produce a vitrified grinding wheel that has excellent grinding performance and is made of alumina sintered abrasive grains with submicron microcrystals, it is necessary to first prepare an alumina gel 1250 particles
It was necessary to calcinate at ~1400°C to produce abrasive grains (loose grains) consisting of microcrystals of aAβ203, add a vitrified binder thereto, and calcinate at about 1220°C.

この方法は一つには1250〜1400℃で−度エネル
ギーを加え、更に1220℃で熱エネルギーを加えると
いう重大なエネルギーの浪費を要するという欠点が有り
、今一つには砥石焼成過程で砥粒を構成する微結晶の成
長を避けるために最も一般的に用いられる性能のよいビ
トリファイドボンド(1300℃前後で用いられる)が
使えないことである。
One disadvantage of this method is that it requires significant energy wastage by applying -degree energy at 1250 to 1400℃ and then thermal energy at 1220℃, and the other disadvantage is that the abrasive grains are formed during the grindstone firing process. In order to avoid the growth of microcrystals, the most commonly used high-performance vitrified bond (used at around 1300° C.) cannot be used.

[発明が解決しようとする課題1 本発明の目的は前述のエネルギーロスと結晶成長を防ぎ
研削性能の優れた砥石を経済的に製造することにある。
[Problems to be Solved by the Invention 1] An object of the present invention is to prevent the above-mentioned energy loss and crystal growth and to economically produce a grindstone with excellent grinding performance.

[課題を解決するための手段] 本発明者らは上記の目的を達成するために鋭意研究した
結果、焼成すれば砥粒となる粒子を砥材とし、焼成によ
ってつくられる砥石の製造の際、焼成前の砥粒を供する
ことにより、砥粒の焼成を砥石の焼成と同時に行うこと
ができることを見出し、本件発明を完成した。
[Means for Solving the Problems] As a result of intensive research to achieve the above object, the present inventors found that when manufacturing a grindstone made by firing particles that become abrasive grains when fired, the abrasive material is used. The inventors have discovered that by providing unfired abrasive grains, the firing of the abrasive grains can be performed simultaneously with the firing of the whetstone, and the present invention has been completed.

すなわち本件発明の要旨は未焼成砥粒をビトリファイド
ボンドと配合、成形し、砥粒焼成と砥石焼成を同時に行
なうことを特徴とするビトリファイド砥石の製造方法に
ある。
That is, the gist of the present invention resides in a method for producing a vitrified grindstone, which is characterized in that green abrasive grains are blended with vitrified bond, molded, and abrasive grain firing and grindstone firing are performed simultaneously.

この方法の特徴は焼成前の安価な砥材を用いることので
きる他、砥石焼成時の砥粒の変質を防ぐために設けられ
ている砥石焼成温度に関する制約をゆるめることにある
The characteristics of this method include not only the use of inexpensive abrasive material before firing, but also the relaxation of restrictions on the grindstone firing temperature, which are set to prevent deterioration of the abrasive grains during grindstone firing.

このような砥石を作るためにはゲルを500〜1000
℃で仮焼した所定の粒度のアルミナ買主砥粒にビトリフ
ァイドボンドを加え、通常の方法で砥石を焼成すればよ
い。500℃未満ではゲルの水分が十分除去できないた
め砥粒とボンドの結合が弱まり好ましくなく、1000
℃を超えると経済的メリットが余りなくなる。仮焼条件
としては低いほど経済性は良いが焼成した砥石寸法が収
縮のためくるいやずく、逆に仮焼湯度が高い程経済性は
悪いが寸法精度が良くなるという関係にある。
To make a whetstone like this, you need 500 to 1000 gel.
Vitrified bond may be added to alumina buyer abrasive grains of a predetermined particle size calcined at °C, and the abrasive stone may be fired in the usual manner. If the temperature is lower than 500°C, the moisture in the gel cannot be removed sufficiently, which weakens the bond between the abrasive grains and the bond, which is undesirable.
If the temperature exceeds ℃, there will be little economic benefit. The lower the calcination conditions are, the better the economic efficiency is, but the size of the fired whetstone will shrink due to shrinkage, and conversely, the higher the calcination temperature is, the worse the economics will be, but the dimensional accuracy will be better.

従来のゾルゲル法から出発して作られる高アルミナ質多
結晶砥粒を用いてビトリファイド砥石を作る場合、結晶
成長を抑えるため、砥粒焼成速度よりかなり低い温度で
砥石を焼成する必要があった。又、−1に砥粒の変質さ
え起こらなければ砥石焼成温度の高い高温ボンドを用い
る方が砥石の性能が良いとされていた。
When making a vitrified whetstone using high-alumina polycrystalline abrasive grains made starting from the conventional sol-gel method, it was necessary to fire the whetstone at a temperature considerably lower than the abrasive grain firing rate in order to suppress crystal growth. Furthermore, it was believed that the performance of the grindstone would be better if a high-temperature bond with a high grindstone firing temperature was used as long as no deterioration of the abrasive grains occurred in -1.

本発明では、ゾルゲル法の場合、前記したように焼成前
の状態としては水が残らない下限の温度で仮焼されたも
のが望ましい。その方が砥石焼成温度をより高くするこ
とができる。この際砥石焼成温度は1200〜1500
℃が適当である。
In the present invention, in the case of the sol-gel method, as described above, the state before firing is preferably calcined at the lowest temperature at which no water remains. That way, the grindstone firing temperature can be made higher. At this time, the grindstone firing temperature is 1200 to 1500.
°C is appropriate.

又、本発明の製造方法によって得られる別の用途によっ
ては、例えば被研削材の種類に対応して砥粒に一層の硬
さと靭性が要求される場合には、多少経済性を犠牲にし
ても仮焼ゲルを1000〜1250℃の温度に120秒
以内に急熱昇温処理し、90秒以内で温度保持しておく
と急熱処理粒子の硬度は2000未満(ピッカス、荷重
500g)であるが砥石焼成中に2000以上の硬度と
高い靭性が得られる。
Furthermore, depending on other uses obtained by the manufacturing method of the present invention, for example, if the abrasive grains are required to have higher hardness and toughness depending on the type of material to be ground, it may be possible to sacrifice economic efficiency to some extent. If the calcined gel is rapidly heated to a temperature of 1000 to 1250°C within 120 seconds and the temperature is maintained within 90 seconds, the hardness of the rapidly heated particles will be less than 2000 (Picus, load 500g), but it will not work on a grindstone. Hardness of 2000 or more and high toughness are obtained during firing.

すなわちこの場合の利点は砥粒段階での収縮が大きい(
比重35→398)ので砥石の寸法精度が高まること及
び砥粒の急熱時α−Aρ203の核が多数発生して微細
結晶となり砥粒の靭性が増加することである。
In other words, the advantage in this case is that the shrinkage at the abrasive grain stage is large (
The specific gravity increases from 35 to 398), so the dimensional accuracy of the grindstone increases, and when the abrasive grains are rapidly heated, a large number of α-Aρ203 nuclei are generated and become fine crystals, increasing the toughness of the abrasive grains.

尚、本発明でビトリファイドボンドとはSiO3、A(
2203、NazOl K2O、CaO1その他少量の
成分を含んだ組成物を約10μの粉末にし、約1200
℃で15分程度加熱溶融し、冷却後、再び粉砕して約1
0μの粉末にしたものをいう。ただ溶融、再粉砕は必ず
しも必要ない。例えば砥粒とボンドとの過度の反応(多
少の反応がないと結合力がでないが)を抑えるためには
溶融、再粉砕が必要であるが、本発明の大部分の方法で
はその必要はない。これは仮焼ゲルが微結晶α−Af2
2o3を構成する方がボンドと反応するよりも有利であ
るためと考えられる。
In the present invention, vitrified bond refers to SiO3, A(
2203, NazOl A composition containing K2O, CaO1 and other small amounts was made into a powder of about 10μ, and
Melt by heating at ℃ for about 15 minutes, cool down, and crush again to give about 1
This refers to powder that has a particle size of 0μ. However, melting and re-grinding are not necessarily necessary. For example, melting and re-grinding are necessary to suppress excessive reaction between the abrasive grains and the bond (bonding strength is lost without some reaction), but this is not necessary in most of the methods of the present invention. . This is because the calcined gel is microcrystalline α-Af2
This is thought to be because forming 2o3 is more advantageous than reacting with the bond.

又、焼成すれば砥粒となる粒子に予め酸化クロムを塗布
しておくことにより砥粒部分はルビー色となりルビー砥
石が得られる。
Further, by applying chromium oxide in advance to particles that become abrasive grains when fired, the abrasive grain portions become ruby-colored and a ruby abrasive stone is obtained.

[実施例1] 次の配合から成る三種の混合物を作った。[Example 1] Three mixtures were made with the following formulations:

混合物1: 500℃、12時間仮焼した840〜1410LLのア
ミナゲルを3g、ビトリファイドボンドを1g混合物2
ニ ア50℃、4時間仮焼した840〜1410μのアミナ
ゲルを3g、ビトリファイドボンドを1g混合物3: 1000℃、1時間仮焼した840〜1410μのアミ
ナゲルを3g、ビトリファイドボンドを1g尚、ビトリ
ファイドボンドとしては5iOJ6%、i□0312%
、 Ca09%、Na2O2%、K2O3%、その他少
量の酸化物を含むものを一旦1400 ’Cで溶解し、
約10LLに粉砕したものを用いた。
Mixture 1: 3 g of 840-1410 LL amine gel calcined at 500°C for 12 hours, 1 g of vitrified bond Mixture 2
Mixture 3: 3 g of 840-1410 μm amine gel calcined at 50°C for 4 hours and 1 g of vitrified bond. 5iOJ6%, i□0312%
, Ca09%, Na2O2%, K2O3%, and other substances containing small amounts of oxides were once dissolved at 1400'C,
The powder was ground to about 10 LL.

これら3種の混合物にアラビアゴム水溶液を添加して約
20mmφX10mmのベレットに成形し、マツフル炉
に入れ11時間で1350℃に昇温し、1350”Cで
2時間保持してから9時間で室温にもどし、でき−につ
たベレット状砥石の各々に付き半分に切断してから鏡面
研摩し砥粒部分のマイクロピッカス硬さを荷重500g
で測定したところ三種とも2100kg/mm″であっ
た。次いでこれら切断したもうつの塊りを粉砕してX線
回折したところαA!2203のみが検出されボンドと
砥粒が反応した際生じると思われるムライト等は同定さ
れなかった。
An aqueous solution of gum arabic was added to the mixture of these three types, formed into pellets of about 20 mmφ x 10 mm, placed in a Matsufuru furnace, heated to 1350°C for 11 hours, held at 1350”C for 2 hours, and then brought to room temperature in 9 hours. Cut each of the returned pellet-shaped grindstones in half, then mirror-polish them to a micro-picchus hardness of the abrasive grains under a load of 500 g.
When measured, all three types were 2100 kg/mm''.Then, when these cut lumps were crushed and subjected to X-ray diffraction, only αA!2203 was detected, which is thought to be generated when the bond and abrasive grains react. Mullite etc. were not identified.

[実施例2] 実施例1で仮焼したアルミナゲルとして予め0.3uの
CrzOaをゲルに対して1%塗布したものを用い、他
は実施例1と同様にしてベレット状砥石を焼成したとこ
ろ砥粒部分はルビー色となりルビー砥石が得られた。
[Example 2] A pellet-shaped grindstone was fired in the same manner as in Example 1 except that the alumina gel calcined in Example 1 was coated with 0.3 u of CrzOa at 1% to the gel in advance. The abrasive grains became ruby colored and a ruby abrasive stone was obtained.

[実施例31 実施例1に於ける混合物2に用いたと同じロットのアル
ミナゲルを小型ロータリーキルンで熱処理した。熱処理
の条件は原料をフィード端(室温)から均熱端(119
0℃)まで60秒で到達させ、熱均帯(1190℃)を
60秒で通過させ、キルン外に排出し冷却するものであ
った。
[Example 31 The same lot of alumina gel used in Mixture 2 in Example 1 was heat treated in a small rotary kiln. The heat treatment conditions are as follows: the raw material is transferred from the feed end (room temperature) to the soaking end (119
0° C.) in 60 seconds, passed through a thermal zone (1190° C.) in 60 seconds, and was discharged outside the kiln for cooling.

次に熱処理済の粒子3gにビトリファイドボンド  (
310265% 、   Aj2 203 25% 、
  Na204.5% 、   K2[)35%、Ca
00.5%、その他少量成分)Igを加え少量のアラビ
アゴム水溶液を添加してよく練ってから約20闘φX1
.Ommのベレットに成形した。
Next, 3g of heat-treated particles were bonded with vitrified bond (
310265%, Aj2 203 25%,
Na204.5%, K2[)35%, Ca
00.5%, other small amounts of ingredients) Add Ig and a small amount of gum arabic aqueous solution, mix well, and mix about 20 mm x 1
.. It was molded into a 0mm pellet.

ベレットを乾燥後マツフル炉に入れ10時間で1150
℃に昇温し、この温度で10時間保持した後9時間で室
温に戻した。実施例1と同様にしてベレットの砥粒を調
べたところマイクロピッカス硬度2300 (荷重50
0g)、結晶の大きさ 18!1(SEM写真より求め
た平均値)であった。又、ベレットの一部を約10LL
に粉砕してX線回折試料としたが粒子とポンドが反応し
て生じると考えられるムライト等の化合物は同定されな
かった。
After drying the pellet, put it in the Matsufuru furnace and it will become 1150 in 10 hours.
The temperature was raised to .degree. C., maintained at this temperature for 10 hours, and then returned to room temperature in 9 hours. When the abrasive grains of the pellet were examined in the same manner as in Example 1, the micropicchus hardness was 2300 (load 50
0g), and the crystal size was 18!1 (average value determined from SEM photographs). Also, a part of the beret is about 10LL
The particles were crushed to obtain an X-ray diffraction sample, but compounds such as mullite, which are thought to be produced by the reaction between particles and pounds, were not identified.

[発明の効果] 本発明に係るビトリファイド砥石の製造方法によりビト
リファイドボンドを制約なく使用硬度の高い砥石を製造
することができる。
[Effects of the Invention] According to the method for producing a vitrified grindstone according to the present invention, a grindstone with high hardness can be produced using vitrified bond without any restrictions.

Claims (3)

【特許請求の範囲】[Claims] (1)未焼成砥粒をビトリファイドボンドと配合、成形
し、砥粒焼成と砥石焼成を同時に行なうことを特徴とす
るビトリファイド砥石の製造方法。
(1) A method for producing a vitrified whetstone, which comprises blending green abrasive grains with vitrified bond, molding the mixture, and simultaneously firing the abrasive grains and firing the whetstone.
(2)未焼成砥粒が、予め1000℃以上1250℃以
下の温度に120秒以内で到達させ90秒以内で保持す
る急熱処理した粒子である請求項1記載のビトリファイ
ド砥石の製造方法。
(2) The method for producing a vitrified grindstone according to claim 1, wherein the unfired abrasive grains are particles that have been subjected to a rapid heat treatment in which the unfired abrasive grains are heated in advance to a temperature of 1000° C. to 1250° C. within 120 seconds and maintained within 90 seconds.
(3)未焼成砥粒が、予め酸化クロムを塗布したもので
ある請求項1記載のビトリファイド砥石の製造方法。
(3) The method for producing a vitrified grindstone according to claim 1, wherein the unfired abrasive grains are coated with chromium oxide in advance.
JP8782289A 1989-04-06 1989-04-06 Manufacture of vitrified grinding wheel Pending JPH02269567A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8782289A JPH02269567A (en) 1989-04-06 1989-04-06 Manufacture of vitrified grinding wheel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8782289A JPH02269567A (en) 1989-04-06 1989-04-06 Manufacture of vitrified grinding wheel

Publications (1)

Publication Number Publication Date
JPH02269567A true JPH02269567A (en) 1990-11-02

Family

ID=13925650

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8782289A Pending JPH02269567A (en) 1989-04-06 1989-04-06 Manufacture of vitrified grinding wheel

Country Status (1)

Country Link
JP (1) JPH02269567A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06335866A (en) * 1993-05-26 1994-12-06 Noritake Co Ltd Vitrified grinding wheel and manufacture thereof
US6086467A (en) * 1997-06-30 2000-07-11 Toyoda Koki Kabushiki Kaisha Grinding wheel

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06335866A (en) * 1993-05-26 1994-12-06 Noritake Co Ltd Vitrified grinding wheel and manufacture thereof
US6086467A (en) * 1997-06-30 2000-07-11 Toyoda Koki Kabushiki Kaisha Grinding wheel

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