JPS58113285A - Alumina abrasive - Google Patents

Alumina abrasive

Info

Publication number
JPS58113285A
JPS58113285A JP56209915A JP20991581A JPS58113285A JP S58113285 A JPS58113285 A JP S58113285A JP 56209915 A JP56209915 A JP 56209915A JP 20991581 A JP20991581 A JP 20991581A JP S58113285 A JPS58113285 A JP S58113285A
Authority
JP
Japan
Prior art keywords
abrasive grains
soda
sulfuric acid
alumina
alumina 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.)
Granted
Application number
JP56209915A
Other languages
Japanese (ja)
Other versions
JPH0235795B2 (en
Inventor
Masakazu Maki
牧 昌和
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 JP56209915A priority Critical patent/JPS58113285A/en
Publication of JPS58113285A publication Critical patent/JPS58113285A/en
Publication of JPH0235795B2 publication Critical patent/JPH0235795B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To prevent the separation of sodium component from the alumina abrasive grains in a resinoid abrasive wheel, and prevent the lowering of the strength of the wheel, by attaching a specific amount of sulfate group to the grain. CONSTITUTION:Alumina abrasive grains are immersed in a dilute aqueous solution of sulfuric acid (preferably 0.01-4mol/l) e.g. at room temperature for >=10min, washed with water under the condition to leave 5-2,000ppm of the sulfate group on the grain, and dried preferably at <=300 deg.C.

Description

【発明の詳細な説明】 本発明は溶融アルミナ砥粒、焼結アルミナ砥粒に関し、
さらに詳しくはこれら砥粒に特定量の硫酸根が付着して
いるアルミナ砥粒に関する。
[Detailed Description of the Invention] The present invention relates to fused alumina abrasive grains and sintered alumina abrasive grains,
More specifically, the present invention relates to alumina abrasive grains having a specific amount of sulfuric acid radicals attached to these abrasive grains.

バイヤーアルミナを原料とするアルミナ砥粒は、バイヤ
ーアルミナにソーダ分が含まれているので、ソーダの混
入が避けられない。
Alumina abrasive grains made from Bayer alumina contain soda, so contamination with soda is unavoidable.

アルミナ砥粒にソーダが混入していると、その砥粒を用
いてレジノイド砥石を製造した場合・砥石の強度、脣に
水浸漬後の強度を弱める欠点が生ずる。レジノイド砥石
のレジンは最も多くはフェノール樹脂が使用されている
が、その他エポキシ樹脂、不飽和ポリエステル樹脂等も
少量使用されている。これらの中では特にフェノール樹
脂がソーダの影響が大きいが、エポキシ樹脂等にも影響
は現れる。ソーダを含有した砥粒を用いた砥石の水浸漬
強度が低下するのはソーダとレジンが反応し、水可溶性
の化合物が生ずることが一つの原因と云われている。
If soda is mixed into alumina abrasive grains, the strength of the abrasive stone will be weakened when a resinoid whetstone is manufactured using the abrasive grains, and the strength after immersion in water will be weakened. Phenol resin is most often used as the resin for resinoid grinding wheels, but small amounts of other resins such as epoxy resin and unsaturated polyester resin are also used. Among these, phenolic resins are particularly affected by soda, but epoxy resins and the like are also affected. It is said that one of the reasons why the water immersion strength of a whetstone using abrasive grains containing soda decreases is that the soda and resin react to form a water-soluble compound.

従来から砥粒のソーダ分低減化の方策は棟々提案されて
いるが、絶無とすることはできない。従来の方法は原料
アルミナのソーダ分を下げること、溶融あるいは焼結の
除、脱ソーダ化をはかること、溶融あるいは焼結後粉砕
して粒状としてから塩酸等で処理するのが一般的である
。しかし、これらの処理によってもソーダはNa2Oと
して少ない場合でも002重tS程度は含有している。
Many measures have been proposed to reduce the soda content of abrasive grains, but they cannot be completely eliminated. Conventional methods generally include lowering the soda content of raw alumina, eliminating melting or sintering, and removing soda, and after melting or sintering, crushing the alumina into granules and then treating the alumina with hydrochloric acid or the like. However, even with these treatments, soda still contains about 002 weight tS even if the amount is small as Na2O.

アルミナ中のソーダは遊離のNa2Oとしてき有してい
るものとβ−アルミナ(Na2O・11A42C15)
の形で含有しているものとの合にである。この中で愼粒
に前記のような問題を起すのは遊離のNa2Oである。
Soda in alumina is present as free Na2O and β-alumina (Na2O・11A42C15)
This is the case when it is contained in the form of Among these, it is free Na2O that causes the above-mentioned problems in the grains.

これらのソーダ分は砥粒の表面のみならず、内部にも吸
蔵されており、この吸蔵されたソーダ分は酸洗等によっ
ては除去が困難である、。
These soda components are occluded not only on the surface of the abrasive grains but also inside them, and it is difficult to remove these occluded soda components by pickling or the like.

そしてアルミナ砥粒のソーダ分が厄介なのはこの吸蔵さ
れたソーダ分が酸洗後の乾燥工程あるいは砥石の製造工
程において、砥粒の表面に析出して来、それが前記のよ
うな問題を引き起すことである。このことは砥粒を酸洗
、次いで十分水洗した後乾燥し、それを水に浸してその
PHを測定してみるとアルカリ性を呈することからもわ
かる。
The trouble with the soda content of alumina abrasive grains is that this occluded soda content precipitates on the surface of the abrasive grains during the drying process after pickling or during the grindstone manufacturing process, which causes the problems mentioned above. That's true. This can be seen from the fact that when the abrasive grains are pickled, then thoroughly washed with water, dried, immersed in water, and the pH is measured, the abrasive grains exhibit alkalinity.

従って、ば洗、乾燥をくり返せばNa2Oをかなり低減
させることは可能である。しかしこの操作のくり返しは
工業的には非常に不利である。
Therefore, by repeating washing and drying, it is possible to significantly reduce Na2O. However, repeating this operation is very disadvantageous industrially.

本発明はこのような事情のもとに開発した砥粒で、レジ
ノイド砥石におけるアルミナ砥粒のソーダ分による弊害
を防止することを目的とし、そのためにアルミナ砥粒を
酸洗、特に硫酸水溶液で処理した後、硫酸@(SO4)
を砥粒に5〜2000 PPM付着させておくことを特
徴とする。
The present invention is an abrasive grain developed under these circumstances, and the purpose is to prevent the harmful effects of the soda content of alumina abrasive grains in resinoid grinding wheels.For this purpose, the alumina abrasive grains are acid-washed, particularly treated with an aqueous sulfuric acid solution. After that, sulfuric acid @(SO4)
It is characterized in that 5 to 2000 PPM of is attached to the abrasive grains.

一般にアルミナ砥粒の酸洗によるソーダ分の除去には酸
として塩酸が使用されている。処理後は水洗、乾燥して
製品とされる。この製品となった状態では塩ばは付着し
てなく、そこにソーダ分のPHi測ればアルカリ性を呈
する。
Generally, hydrochloric acid is used as the acid to remove the soda content by pickling alumina abrasive grains. After processing, the product is washed with water and dried. In this product state, there is no salt attached, and if you measure the PHi of the soda content, it will show alkalinity.

砥粒を硫酸で処理しても乾燥温度が高かったり或いは水
洗を十分よく行なえば硫酸根は痕跡程度しか残らない。
Even if the abrasive grains are treated with sulfuric acid, only traces of sulfuric acid radicals will remain if the drying temperature is high or if the abrasive grains are washed thoroughly with water.

従って前記同様乾燥後の砥粒の浸漬水溶液はアルカリ性
である。
Therefore, as described above, the aqueous solution in which the abrasive grains are immersed after drying is alkaline.

本発明はこのvC酸根を砥粒に特定蓋付涜させておくも
のであり、そのためには砥粒の硫葭処理後の水洗、乾燥
条件等を選ぶことが必要である。憾酸の代りに塩酸処理
では乾燥後塩化水素を砥粒に特定量付着させておくこと
が困難で、kmlと同体の効果は現れなかった。
In the present invention, this vC acid radical is attached to the abrasive grains in a specific manner, and for this purpose, it is necessary to select the washing conditions, drying conditions, etc. after the abrasive grains are treated with sulfur. When treated with hydrochloric acid instead of acetic acid, it was difficult to keep a specific amount of hydrogen chloride attached to the abrasive grains after drying, and the same effect as kml did not appear.

本発明において硫酸根の付着量は804として5PPM
より少ないと後に実施例に・示すように効果が明確に現
れず、また2000 P P Mを越えると(フェノー
ル樹脂は弱酸にはあまりおかされないが、強酸には若干
おかされるため)フェノール樹脂が硫酸におかされる咎
の欠点が生ずる。
In the present invention, the amount of attached sulfate roots is 5PPM as 804.
If the amount is less, the effect will not be clearly seen as shown in the examples later, and if it exceeds 2000 P P M (because phenol resin is not affected much by weak acids, but is slightly affected by strong acids), the phenol resin becomes The disadvantages of being exposed to sulfuric acid arise.

硫酸根が砥粒に付着されていることにより、何故にレジ
ノイド砥石の強度低下を来たさないがは定かでない耘、
一つの理由は析出して来たソーダが硫酸イオンと反応し
、硫酸塩が生成し、遊離のソーダによるレジンの浸食を
防止するためと考えられる。その二は砥粒表面に付着し
ているものがmat塩であってもこの侵食防止効果が認
められるところより、砥粒とレジンの界面に硫酸根が存
在することにより、何らかの作用で新たに析出したソー
ダ分のレジン侵食を抑制するものと考えられる。この硫
酸塩が付着している状態では、これにさらにソーダ分の
析出が加わっているので、この砥粒の水浸漬溶液はアル
カリ性である。
It is unclear why the strength of the resinoid grinding wheel does not decrease due to the sulfuric acid radicals attached to the abrasive grains.
One reason is thought to be that the precipitated soda reacts with sulfate ions to generate sulfate, which prevents erosion of the resin by free soda. The second reason is that even if mat salt adheres to the surface of the abrasive grains, this corrosion prevention effect is observed, and due to the presence of sulfuric acid groups at the interface between the abrasive grains and the resin, new precipitation occurs due to some action. It is thought that this suppresses the resin corrosion caused by the soda content. In the state in which this sulfate is attached, the water immersion solution of the abrasive grains is alkaline because a soda component is further precipitated.

本発明において砥粒に付着している硫酸根は硫酸の形で
存在していることが最も望ましいが、硫ばソーダ等の塩
の形であっても効果が認められ、従って本発明にはこれ
らも含む。
In the present invention, it is most desirable that the sulfuric acid radicals attached to the abrasive grains exist in the form of sulfuric acid, but the effect is recognized even in the form of salts such as sulfuric acid and soda. Also included.

本発明の砥粒を得るには粉砕後、所定の粒度に分級した
砥粒を希硫酸水浴液に浸漬する。この場合の条件は特に
制限ないが、取扱い易さ、処理効率寺より憾酸の震度は
001〜4モル/1%温度は室温でよく、時間は10分
間以上が適当である。
To obtain the abrasive grains of the present invention, after pulverization, the abrasive grains are classified into a predetermined particle size and immersed in a dilute sulfuric acid water bath. The conditions in this case are not particularly limited, but from the viewpoint of ease of handling and treatment efficiency, the intensity of acetic acid is 0.01 to 4 mol/1%, the temperature may be room temperature, and the time is preferably 10 minutes or more.

浸漬後、砥粒を水洗、乾燥する。この条件は砥粒の眞酸
根が前記の範囲に入るように選ぶ。乾燥は高温だと硫酸
が揮発あるいは分解し、本発明の範囲内の硫酸根を付着
させることができなくなるので、望ましい乾燥温度は3
00℃以下である。。
After soaking, the abrasive grains are washed with water and dried. These conditions are selected so that the sulfuric acid radical of the abrasive grains falls within the above range. If the drying temperature is high, the sulfuric acid will volatilize or decompose, making it impossible to attach the sulfuric acid groups within the scope of the present invention, so the desirable drying temperature is 3.
The temperature is below 00℃. .

実施例 溶融アルミナ砥粒(粒度はJIS+60番、Na2O総
量0.06重量%)、100重量部を希114 モ/L
、/l) 150重量部に20℃で、120分間浸漬し
、次いで水洗回数を櫨々変え、また乾燥温度を100〜
200℃の範囲で選んで砥粒に残留すi so4イオン
の量を第1表に示す値になるように調整した。との砥粒
とフェノール樹脂を用いて通常の砥石と同様次のように
配合し、成形、硬化してテストピースを作成した。
Example Fused alumina abrasive grains (particle size: JIS+60, total amount of Na2O 0.06% by weight), 100 parts by weight diluted with 114 mo/L
, /l) at 20°C for 120 minutes, then the number of water washes was changed constantly, and the drying temperature was changed from 100°C to 100°C.
The amount of iso4 ions remaining in the abrasive grains was selected within the range of 200°C and adjusted to the values shown in Table 1. A test piece was created by mixing the abrasive grains and phenol resin in the same way as a regular whetstone as follows, molding and hardening.

砥粒                  100(重
址部)液状樹脂(昭和ユニオン合成■BRL−207)
t、s粉末樹脂(BRP−503) 65 硬化後のテストピースの嵩比重は2,05であった。
Abrasive grain 100 (heavy part) Liquid resin (Showa Union Synthesis ■BRL-207)
t, s powder resin (BRP-503) 65 The bulk specific gravity of the test piece after curing was 2.05.

このテストピースの抗折力(乾式抗折力)及びこれと同
じものを40℃の温水に24時間浸漬した後の抗折力(
湿式抗折力)を測定した。結果を第2表に示す。なお、
酸洗、乾燥後のNa2Oの量は約0.05重賞チであっ
た。
The transverse rupture strength of this test piece (dry transverse rupture strength) and the transverse rupture strength after immersing the same test piece in 40°C hot water for 24 hours (
Wet transverse rupture strength) was measured. The results are shown in Table 2. In addition,
The amount of Na2O after pickling and drying was approximately 0.05%.

第    2    表 同様に焼結アルミナ砥粒について、酸洗後代酸根を全く
残さなかった場合と200PPM残留付着させり場合と
で前記にならって抗折力を比較した0 硫酸根なし  160    40 硫酸根残留  179    83 以上のように砥粒に硫酸根を残留させたものはピースの
抗折力が大であり、そして特に湿式抗折力の低下が小さ
い。砥石は一般に水等の研削液をかけながら使用される
ので、湿式抗折力は重要な要件である。本発明はこの要
件を満たすものであるO 出願人 昭和電工株式会社 代理人   菊  地  精  −
Similar to Table 2, the transverse rupture strength of sintered alumina abrasive grains was compared between cases in which no acid roots were left after pickling and cases in which 200 PPM residual adhesion was carried out. 0 No sulfate roots 160 40 Sulfate roots remaining 179 83 As described above, the pieces in which sulfuric acid radicals remain in the abrasive grains have a large transverse rupture strength, and the drop in wet transverse rupture strength is particularly small. Since grinding wheels are generally used while being sprayed with a grinding fluid such as water, wet transverse rupture strength is an important requirement. The present invention satisfies this requirement.O Applicant: Showa Denko K.K. Agent Sei Kikuchi -

Claims (1)

【特許請求の範囲】[Claims] 硫酸根が5〜2000PPM付着しているアルミナ砥粒
Alumina abrasive grains with 5 to 2000 PPM of sulfate radicals attached.
JP56209915A 1981-12-28 1981-12-28 Alumina abrasive Granted JPS58113285A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56209915A JPS58113285A (en) 1981-12-28 1981-12-28 Alumina abrasive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56209915A JPS58113285A (en) 1981-12-28 1981-12-28 Alumina abrasive

Publications (2)

Publication Number Publication Date
JPS58113285A true JPS58113285A (en) 1983-07-06
JPH0235795B2 JPH0235795B2 (en) 1990-08-13

Family

ID=16580760

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56209915A Granted JPS58113285A (en) 1981-12-28 1981-12-28 Alumina abrasive

Country Status (1)

Country Link
JP (1) JPS58113285A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61278587A (en) * 1985-06-04 1986-12-09 Fujimi Kenmazai Kogyo Kk Polishing composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61278587A (en) * 1985-06-04 1986-12-09 Fujimi Kenmazai Kogyo Kk Polishing composition
JPS64436B2 (en) * 1985-06-04 1989-01-06 Fujimi Kenmazai Kogyo Kk

Also Published As

Publication number Publication date
JPH0235795B2 (en) 1990-08-13

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