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JPH07266B2 - Whetstone - Google Patents
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JPH07266B2 - Whetstone - Google Patents

Whetstone

Info

Publication number
JPH07266B2
JPH07266B2 JP1008879A JP887989A JPH07266B2 JP H07266 B2 JPH07266 B2 JP H07266B2 JP 1008879 A JP1008879 A JP 1008879A JP 887989 A JP887989 A JP 887989A JP H07266 B2 JPH07266 B2 JP H07266B2
Authority
JP
Japan
Prior art keywords
weight
grindstone
phenol resin
epoxy compound
binder
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
JP1008879A
Other languages
Japanese (ja)
Other versions
JPH02190268A (en
Inventor
康治 山野
Original Assignee
月星化成株式会社
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 月星化成株式会社 filed Critical 月星化成株式会社
Priority to JP1008879A priority Critical patent/JPH07266B2/en
Publication of JPH02190268A publication Critical patent/JPH02190268A/en
Publication of JPH07266B2 publication Critical patent/JPH07266B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Polishing Bodies And Polishing Tools (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明は砥石に関する。特にバレル研磨やブラスト加工
用に小粒砥石として使用するのに適する。
TECHNICAL FIELD The present invention relates to a grindstone. Particularly suitable for use as a small-grained grindstone for barrel polishing and blasting.

従来の技術 フェノール樹脂を結合材とする砥石はよく知られてい
る。バレル研磨に用いるメディアとして球状,円錐上,
円筒状,立方状,無定形,その他の総じて粒状砥石があ
るが、無機物を結合材とするか熱可塑性合成樹脂を結合
材とするものである。フェノール樹脂は砥粒との接着力
もよく耐熱性もあり、無機物に比して弾性率が低く靱性
があるのでワークと砥石の衝突、ずり時に無機物ほどワ
ークをシャープに疵つけないからみがき作用に優れる。
しかしフェノール樹脂は熱硬化性であるためモールド成
型をする必要があり小粒状の砥石のモールド成型は実際
上不可能である。従って、モールドを使わない開放状態
での成形が望まれていた。粉末状で提供されるフェノー
ル樹脂に砥粒を混合し加熱すると、軟化点でフェノール
樹脂が軟化溶融し、その後次第に硬化して変形しなくな
る。砥粒が多い場合、例えば砥粒が80重量%フェノール
樹脂粉末20重量%配合物の場合、アルコールを若干添加
すれば細工用粘土に似た可塑体となりシート状に延展可
能となるから、これを分割して立方状や球状に加工し、
アルコールを揮散させ、そのままオーブン内で加熱すれ
ば粒状の砥石を得ることができる。但し、アルコールの
揮散が困難で残留すれば砥石に空隙ができる。更に砥粒
の比率が70重量%、60重量%と下がってくるとオーブン
内での加熱に当たり、フェノール樹脂の軟下点で流動が
起こって所定形状に加工された粒状配合物が変形する。
2. Description of the Related Art A grindstone using a phenol resin as a binder is well known. The media used for barrel polishing is spherical, on a cone,
Cylindrical, cubic, amorphous, and other types of granular whetstones are generally used, but inorganic materials are used as binders or thermoplastic synthetic resins are used as binders. Phenolic resin has good adhesion to abrasive grains, heat resistance, and has a toughness that is lower than that of inorganic materials and has a toughness, so it does not scratch the work as sharply as an inorganic material when it collides with the work piece and when it slides .
However, since phenol resin is thermosetting, it is necessary to mold it, and it is practically impossible to mold a small grindstone. Therefore, molding in an open state without using a mold has been desired. When the abrasive particles are mixed with the phenolic resin provided in the form of powder and heated, the phenolic resin softens and melts at the softening point, and then gradually hardens and does not deform. If there are many abrasive grains, for example, if the abrasive grains are 80% by weight phenol resin powder 20% by weight compound, adding a little alcohol makes it a plastic material similar to clay for work and can be spread into a sheet. Divide into cubes and spheres,
A granular grindstone can be obtained by volatilizing alcohol and heating in an oven as it is. However, if the alcohol is difficult to volatilize and remains, a void will be created in the grindstone. Further, when the ratio of the abrasive grains decreases to 70% by weight and 60% by weight, upon heating in an oven, fluidization occurs at the softening point of the phenol resin, and the granular compound processed into a predetermined shape is deformed.

従来、フェノール樹脂を結合材とする小粒の砥石を開放
状態で加熱硬化させるにはこのような問題があった。
Conventionally, there has been such a problem in heating and hardening a small grindstone using a phenol resin as a binder in an open state.

問題を解決するための手段 本発明は砥石中で結合材が45容量%を超え、且つ前記結
合材はフェノール樹脂75〜45重量%、グリセリンポリグ
リシジルエーテルのエポキシ化合物25〜55重量%の組成
をもつことを特徴とする砥石を特徴とする。
Means for Solving the Problems The present invention provides a composition in which a binder exceeds 45% by volume in a grindstone, and the binder comprises 75 to 45% by weight of a phenol resin and 25 to 55% by weight of an epoxy compound of glycerin polyglycidyl ether. Characterized by a grindstone characterized by having.

効果 (1)結合材をフェノール樹脂75〜45重量%、エポキシ
化合物25〜55重量%の組成としたので砥粒と結合材の配
合物は、砥粒濃度が低い場合においても加熱に際してフ
ェノール樹脂の軟化点で流動しない。
Effects (1) Since the binder has a composition of 75 to 45% by weight of a phenol resin and 25 to 55% by weight of an epoxy compound, the mixture of the abrasive and the binder has a composition of the phenol resin during heating even when the abrasive concentration is low. Does not flow at the softening point.

従って、配合物は所定の形状を保ったまま開放状態でし
かも重ねて加熱硬化することができる。
Therefore, the composition can be heat-cured in an open state while maintaining a predetermined shape, and by overlapping.

(2)エポキシ化合物が液状であるため粉体であるフェ
ノール樹脂及び砥粒の分散媒となって砥粒濃度が高い配
合物の場合でも配合物を細工用粘土に似た可塑体となし
加工を容易にする。揮発物がないので加熱による砥石内
の空隙が生じない。
(2) Since the epoxy compound is a liquid, it becomes a dispersion medium for the powdery phenolic resin and the abrasive grains, and even if the compound has a high abrasive grain concentration, the compound should be treated with a plastic similar to clay for work without processing. make it easier. Since there are no volatiles, no voids are created in the grindstone due to heating.

(3)上記(1),(2)の効果によって配合物を所定
形状の小粒に加工し、モールドを使用せずに安価な小粒
砥石を提供できる。
(3) Due to the effects of the above (1) and (2), the compound can be processed into small particles having a predetermined shape, and an inexpensive small-sized grindstone can be provided without using a mold.

具体的な説明 本発明に使用される砥石は、アルミナ,炭化珪素,その
他の砥粒で、特に限定されるものではない。フェノール
樹脂はノボラック型で、一般に粉末として供され、既に
ヘキサメチレンテトラミンなど硬化剤を添加配合してあ
るのが普通である。エポキシ化合物は、グリシジル基が
2又は3以上存在する液状の化合物を用いる。ジエポキ
シ化合物としては、例えば骨格がポリエチレン,ポリプ
ロピレン,ポリテトラメチレン,レゾルシン,ネオペン
チルグリコール,1.6ヘキサン,ジオール,ビスフェノー
ルA,アジピン酸,フタル酸で形成されたジグリシジルエ
ーテルなどがあり、ポリエポキシ化合物には、骨格がソ
ルビトール,グリセロール、ジグリセロール,ポリグリ
セロール,ペンタエリスリトール,トリメチルプロパン
で形成されたポリグリシジルエーテルなどがある。
Detailed Description The grindstone used in the present invention is alumina, silicon carbide, or other abrasive grains, and is not particularly limited. Phenolic resin is a novolak type and is generally provided as a powder, and it is usual that a curing agent such as hexamethylenetetramine has already been added and blended. As the epoxy compound, a liquid compound having 2 or 3 or more glycidyl groups is used. Examples of diepoxy compounds include polyethylene, polypropylene, polytetramethylene, resorcin, neopentyl glycol, 1.6 hexane, diol, bisphenol A, adipic acid, diglycidyl ether formed by phthalic acid, and the like. Examples include polyglycidyl ether having a skeleton of sorbitol, glycerol, diglycerol, polyglycerol, pentaerythritol, and trimethylpropane.

フェノール樹脂75〜45重量%、エポキシ化合物25〜55の
結合材と砥粒を混合すると液状のエポキシ化合物が分散
媒の役割を果して可塑状を呈する。可塑状になった配合
物を20〜30℃の温度に放置するとゲル化が進行しエポキ
シ化合物の種類によるが、数十分から数時間でかなり粘
度が上昇する。ゲル化の進行が遅いものは、フェノール
樹脂の軟化点より低い温度で加温してゲル化を促進する
ことができる。可塑性がある間にシートに圧延してこれ
を適宜に分割し、立方粒状としたり更にそれを丸めて球
状としたり、或いは50℃前後で押出機から紐状に押出
し、才断して円筒状とするなど随意に加工する。これを
オーブンに入れて直接180℃に加熱するか、又は段階的
に昇温して180℃で加熱し硬化させる。オーブンに入れ
る前に適宜にゲル化しておれば180℃に直接加熱しても
粒子は変形しない。フェノール樹脂に対するエポキシ化
合物の量は、オーブン加熱中に変形しない程度の最低量
を使用すればよいが、砥粒濃度が50〜55容量%になると
分散媒の役目をするエポキシ化合物の増加を必要とする
ことがある。オーブン加熱に際し、配合物粒子を重ねて
も最下層の粒子が変形荷重以内の荷重しか受けない範囲
で重ねれば、一挙に加熱できる。
When a binder of 75 to 45% by weight of a phenolic resin and 25 to 55 of an epoxy compound is mixed with abrasive grains, the liquid epoxy compound plays a role of a dispersion medium and becomes plastic. When the plasticized mixture is left at a temperature of 20 to 30 ° C, gelation proceeds and the viscosity increases considerably from several tens of minutes to several hours depending on the type of epoxy compound. For those with a slow progress of gelation, the gelation can be promoted by heating at a temperature lower than the softening point of the phenol resin. While it is plastic, it is rolled into a sheet and appropriately divided into cubic particles or it is further rounded into a spherical shape, or it is extruded into a string shape from an extruder at around 50 ° C, and cut into a cylindrical shape. Process it at will. This is placed in an oven and heated directly to 180 ° C, or the temperature is raised stepwise and heated at 180 ° C to cure. Particles do not deform even if directly heated to 180 ° C if gelled appropriately before putting in the oven. The amount of the epoxy compound with respect to the phenol resin may be a minimum amount that does not cause deformation during heating in the oven, but when the abrasive grain concentration reaches 50 to 55% by volume, it is necessary to increase the amount of the epoxy compound that functions as a dispersion medium. I have something to do. In the oven heating, even if the compound particles are piled up, if the particles in the lowermost layer are piled in such a range that only the load within the deformation load is received, they can be heated all at once.

実施例 実施例1 ノボラック型フェノール樹脂粉末レジトップPG(A)‐
2473(群栄科学工業(株)の商品名。硬化剤としてヘキ
サメチレンテトラミンを含有。軟化点84℃)と三官能の
エポキシ化合物SR-GLG(坂本薬品工業(株)の商品名。
グリセリンポリグリシジルエーテル)とアルミナを第1
表の割合で混合した(単位は重量部)。これをNo.1〜3
及び6では室温に約30分放置後シートに圧延して分解
し、丸めて3mmの球形にした。No.4とNo.5は当初粘着性
があるので、室温に8時間放置後同様にして3mmの球形
にする。No.4〜5でも40〜50℃に加熱すれば放置時間を
短縮できる。これを70℃に30分保ったあとガラス容器中
に10cmの高さに入れ180℃のオーブン中で3時間加熱硬
化した。No.1に僅かに変形が認められた外が良好であっ
た。No.1〜5の砥粒濃度は約10容量%,No.6は約50容量
%になる。
Examples Example 1 Novolac-type phenol resin powder cash register top PG (A)-
2473 (Gunei Kagaku Kogyo Co., Ltd .. Hexamethylenetetramine as a curing agent. Softening point 84 ° C) and trifunctional epoxy compound SR-GLG (Sakamoto Yakuhin Kogyo Co., Ltd.).
Glycerin polyglycidyl ether) and alumina first
The ingredients were mixed in the proportions shown in the table (unit is part by weight). This is No. 1-3
In Nos. 6 and 6, the sheet was left standing at room temperature for about 30 minutes, rolled into a sheet, disassembled, and rolled into a spherical shape of 3 mm. Since No. 4 and No. 5 are initially sticky, after leaving them at room temperature for 8 hours, make them 3 mm spherical. Even in Nos. 4 to 5, the standing time can be shortened by heating to 40 to 50 ° C. This was kept at 70 ° C. for 30 minutes, then placed in a glass container at a height of 10 cm, and heat-cured in an oven at 180 ° C. for 3 hours. It was good except that slight deformation was observed in No. 1. The abrasive grain concentration of No. 1 to 5 is about 10% by volume, and that of No. 6 is about 50% by volume.

比較例の場合は第1表の配合にエチルアルコールを8重
量部添加し、同様にシート圧延、分割を経て3mmの球状
とし、30℃で48時間放置後オーブンに入れ、70℃で3時
間加熱後180℃まで徐々に昇温し180℃で3時間加熱硬化
した。
In the case of the comparative example, 8 parts by weight of ethyl alcohol was added to the composition shown in Table 1, similarly rolled into sheets and divided into 3 mm spheres, left at 30 ° C for 48 hours, put in an oven and heated at 70 ° C for 3 hours. After that, the temperature was gradually raised to 180 ° C. and heat-cured at 180 ° C. for 3 hours.

比較例の砥石は変形が大きく、かつ内部に空隙が多かっ
た。
The grindstone of the comparative example was greatly deformed and had many voids inside.

実施例2 エポキシ化合物としてSR-NPG(坂本薬品工業(株)の商
品名、ネオペンチルグリコールジグリシジルエーテ
ル)、SR-TPG(同前、ポリプロピレングリコールジグリ
シジルエーテル)、SR-2EG(同前、ジエチレングリコー
ルジグリシジルエーテル)を用意し、実施例1と同じフ
ェノール樹脂66重量部にそれぞれ33重量部を混合し、ア
ルミナ#1000を90重量部添加混合した。
Example 2 SR-NPG (trade name of Sakamoto Yakuhin Kogyo Co., Ltd., neopentyl glycol diglycidyl ether), SR-TPG (previously, polypropylene glycol diglycidyl ether), SR-2EG (previously, diethylene glycol) as an epoxy compound Diglycidyl ether) was prepared, and 33 parts by weight of each was mixed with 66 parts by weight of the same phenol resin as in Example 1, and 90 parts by weight of alumina # 1000 was added and mixed.

これらのエポキシ化合物の場合は、シート状に圧延でき
る程の粘り気がないので、室温に1時間放置後、押出機
によりノズル温度約50℃で2mmの直径の紐状に押出し、2
mm長さに才断して70℃に1時間保った後、実施例1と同
様方法で加熱硬化させ、変形のない砥石を得た。
Since these epoxy compounds are not sticky enough to be rolled into a sheet, they are left at room temperature for 1 hour and then extruded with an extruder at a nozzle temperature of about 50 ° C into a string with a diameter of 2 mm.
After cutting to a length of mm and holding at 70 ° C. for 1 hour, it was heat-cured in the same manner as in Example 1 to obtain a grindstone without deformation.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】砥石中で結合材が45容量%を超え、前記結
合材はフェノール樹脂75〜45重量%、グリセリンポリグ
リシジルエーテルのエポキシ化合物25〜55重量%の組成
をもつことを特徴とする砥石。
1. A grindstone containing more than 45% by volume of a binder, said binder having a composition of 75-45% by weight of a phenolic resin and 25-55% by weight of an epoxy compound of glycerin polyglycidyl ether. Whetstone.
JP1008879A 1989-01-17 1989-01-17 Whetstone Expired - Lifetime JPH07266B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1008879A JPH07266B2 (en) 1989-01-17 1989-01-17 Whetstone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1008879A JPH07266B2 (en) 1989-01-17 1989-01-17 Whetstone

Publications (2)

Publication Number Publication Date
JPH02190268A JPH02190268A (en) 1990-07-26
JPH07266B2 true JPH07266B2 (en) 1995-01-11

Family

ID=11704959

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1008879A Expired - Lifetime JPH07266B2 (en) 1989-01-17 1989-01-17 Whetstone

Country Status (1)

Country Link
JP (1) JPH07266B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4986590B2 (en) * 2006-12-04 2012-07-25 クレトイシ株式会社 Resinoid grinding wheel

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61152372A (en) * 1984-12-27 1986-07-11 Mitsui Toatsu Chem Inc Synthetic resinous abrasive

Also Published As

Publication number Publication date
JPH02190268A (en) 1990-07-26

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