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JP3795778B2 - Resinoid grinding wheel using hydrogenated bisphenol A type epoxy resin - Google Patents

Resinoid grinding wheel using hydrogenated bisphenol A type epoxy resin Download PDF

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Publication number
JP3795778B2
JP3795778B2 JP2001254232A JP2001254232A JP3795778B2 JP 3795778 B2 JP3795778 B2 JP 3795778B2 JP 2001254232 A JP2001254232 A JP 2001254232A JP 2001254232 A JP2001254232 A JP 2001254232A JP 3795778 B2 JP3795778 B2 JP 3795778B2
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grinding wheel
grinding
abrasive grains
resinoid
synthetic resin
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JP2003062756A (en
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実 林
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Noritake Co Ltd
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Noritake Co Ltd
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Description

【0001】
【発明の属する技術分野】
本発明は、研削砥石における技術分野の中で、特に水添エポキシ樹脂を結合剤として、粒度が#800以上である砥粒が相互に結合されて構成されたレジノイド研削砥石に関する。
【0002】
【従来の技術】
例えば、粗加工等のように取り代の大きい研削加工には、一般に合成樹脂結合剤(レジンボンド)で砥粒を結合したレジノイド研削砥石が用いられる。レジノイド研削砥石がこのような研削に好適に用いられるのは、砥粒を結合する合成樹脂結合剤が、ガラス質結合剤(ビトリファイドボンド)、金属質結合剤(メタルボンド)や電着結合等に比較して弾性率が低いことから、研削加工中に被削材から砥粒に作用する負荷を結合剤の弾性変形によって緩和できる為である。とりわけ、エポキシ樹脂を結合剤として用いたレジノイド研削砥石は、フェノール樹脂を結合剤としたものに比べてより低い弾性率を有し、その特性を活かした上記のような作業の中でも長尺のものや薄肉パイプの加工などに広く使用されている。このようなエポキシ樹脂を結合剤として用いたレジノイド研削砥石の中でも、上記特性を最も顕著に活かすことができるのは、液状のエポキシ樹脂と砥粒等とを混合した後に金型に鋳込む製法により製造されたものであり、エポキシ樹脂の特性である低い弾性率と、この鋳込み製法によって得られる砥粒と結合剤との濡れによる物理的に強固な結合とが相俟って、上記レジノイド砥石に優れた研削性能を付与するものと考えられる。
【0003】
【発明が解決しようとする課題】
しかし、被削材の被削面品位を向上する目的で、粒度が#800以上の微細砥粒を用いたエポキシ樹脂を結合剤とするレジノイド研削砥石では、砥石加工面の切粉の目詰まり及び溶着によって、被削材の被削面に光沢ムラが発生したり、ラセンマークや傷がついてしまう等の理由により、所望の被削材表面品位を継続的に得られず、ドレッシングが頻繁に必要になるという課題があった。
【0004】
本発明は、かかる課題を解決する為に為されたものであり、その目的とするところは、粒度が#800以上といった微細砥粒を用いたレジノイド研削砥石であっても、合成樹脂結合剤が砥粒に対して適度な保持力を有し、切れ刃を自生させて良好な被削材表面品位を継続的に得られるレジノイド研削砥石を提供することにある。
【0005】
【課題を解決する為の手段】
本発明者は、前記課題について検討を続け、粒度が#800以上の微細砥粒を用いたエポキシ樹脂を結合剤とするレジノイド砥石に関し、前記課題が発生するのは、砥粒と結合剤であるエポキシ樹脂との結合が粒度が#800といった微細砥粒には強すぎる為に切れ刃の自生が妨げられるからであるとの見解を持つに至った。すなわち、微細砥粒を用いたレジノイド研削砥石が使用される作業は一般的に研削時の負荷が粗粒の場合と比べて小さいことと、被削材の被削面で研削に関与する砥粒数が微細砥粒の場合は必然的に多くなってしまう結果、砥粒一粒に対する負荷が小さくなる為に、仮に結合剤が砥粒を保持する結合力が微細砥粒と粗粒とで同じだとしても、砥粒を脱落させようとする力が微細砥粒の場合は比較的小さくなる為に切れ刃の適度な自生が起こらないのだと考えた。
【0006】
ところで、エポキシ樹脂による砥粒の結合は、一般的には物理的なカシメによる結合力が支配的であると考えられており、これを小さくするにはエポキシ樹脂単体の弾性率を下げる必要がある。レジノイド研削砥石に合成樹脂結合剤として一般的に用いられるビスフェノールA等を主原料としたエポキシ樹脂の弾性率を下げる為には、製造段階で反応性希釈剤を添加しなければならないが、この反応性希釈剤を添加することにより合成樹脂結合剤の弾性率のみならず耐熱性も下がってしまう為に研削に際して用いられる研削液の温度変化によってレジノイド研削砥石の研削性能がばらつき易くなるなどの砥石の性能に関する新たな問題に加え、レジノイド研削砥石の製造に際し、硬化剤と混合する際の粘度が上昇する為に砥粒との混合が十分に行われず、更には、混合時の撹拌熱によりエポキシ樹脂の硬化を異常促進させるなどの製造上の問題が発生する可能性が考えられる。粒度が#800以上といった微細砥粒との十分な混合状態を得る為の樹脂混合粘度(樹脂を硬化剤と混合した際の粘度)は一般に1Pa・s以下であり、この条件及び研削性能のばらつきを抑える為に、硬化後の単体のガラス転移温度が100℃以上という条件を満たすには、ビスフェノールAといった材料では、硬化後の単体の弾性率は最低でも3GPaとなってしまう。
【0007】
本発明は、以上の事情を背景として為されたものであり、その要旨とするところは、合成樹脂結合剤によって粒度が#800以上である砥粒が相互に結合されて構成されたレジノイド研削砥石であって、前記合成樹脂結合剤は、水添ビスフェノールAを主原料とする主剤を使用するものであり、硬化後の単体のガラス転移温度が100℃以上となるものであることを特徴とするものである。
【0008】
【発明の効果】
このようにすれば、前記合成樹脂結合剤は、水添ビスフェノールAを主原料とする主剤を使用するものであり、硬化後の単体のガラス転移温度が100℃以上となるものであることから、粒度が#800以上といった微細砥粒を用いたレジノイド研削砥石であっても、研削時に用いられる研削液の温度変化などによってレジノイド研削砥石の研削性能がばらつき易くなるなどの砥石の性能に関する問題が発生せず、合成樹脂結合剤が砥粒に対して適度な保持力を有し、切れ刃を自生させて良好な被削材表面品位を継続的に得られるレジノイド研削砥石を提供することができる。
【0009】
【発明の他の態様】
ここで、好適には、前記合成樹脂結合剤は、主剤と硬化剤とを混合した際の粘度が1Pa・s以下となるものである。このようにすれば、レジノイド研削砥石10の製造において、合成樹脂結合剤の主原料と硬化剤とを混合する際の粘度が十分に低い為に砥粒との混合が好適に行われ、混合時の撹拌熱によりエポキシ樹脂の硬化を異常促進させるなどの製造上の問題が発生しない。
【0011】
また、好適には、前記合成樹脂結合剤は、硬化後の単体の曲げ弾性率が2GPa以下となるものである。このようにすれば、粒度が#800以上といった微細砥粒を用いたレジノイド研削砥石であっても、合成樹脂結合剤が砥粒に対して適度な保持力を有し、切れ刃を自生させて良好な被削材表面品位を継続的に得られるレジノイド研削砥石を提供することができる。
【0012】
【実施例】
以下、本発明の一実施例を図面に基づいて詳細に説明する。
【0013】
図1は、本発明の一実施例であるレジノイド研削砥石10の形状を示す斜視図である。図において、レジノイド研削砥石10は、たとえば、外径500(mmφ)×厚さ150(mm)×内径200(mmφ)程度の寸法で全体が一体的に構成された円筒研削型の円盤状砥石であり、中央部に設けられた取り付け穴12において図示しない研削機械の主軸に取り付けられ、外周研削面14と被削材との間に研削液を供給しつつ、図示しない保持装置に保持された被削材を外周研削面14に押しつけた状態で、その軸心回りに回転されて用いられる。これにより、被削材の被削面が外周研削面14により所望形状に研削される。
【0014】
図2は、上記レジノイド研削砥石10の構成を拡大して示す図である。この図において、レジノイド研削砥石10は、SiC、溶融アルミナ等の一般砥粒や、CBN、ダイヤモンド等の超砥粒である砥粒16が、レジンボンドすなわち合成樹脂結合剤18によって相互に結合されることにより、多数の気孔22を備えて構成されている。このように構成されたレジノイド研削砥石10では、上述のようにその外周研削面14が被削材20の被削面24に摺接させられることにより、砥粒16の切れ刃26が被削材20の被削面24を研削する。研削に伴って砥粒16の一部が破砕されると、次の切れ刃26が再生されて研削性能が継続される。上記合成樹脂結合剤18は、専ら砥粒16間を必要且つ十分に結合するように、砥粒16あるいは全体に対する重量割合が決定されており、破砕された砥粒16が小さくなると合成樹脂結合剤18の保持力が低下するので、その破砕された砥粒16と共に脱落して次の砥粒16を研削に関与させるようにする。このとき、砥粒16の番数が大きくなる程すなわち粒径が小さくなるほど研削に関与する切れ刃26が小さくなると同時に切れ刃数が増加する為、砥粒16の粒径が小さくなる程それに見合った平滑な加工物表面品位が得られるようになる。
【0015】
本実施例のレジノイド研削砥石10は、例えば、以下のようにして製造される。先ず、合成樹脂結合剤18として水添ビスフェノールAたとえばヘキサヒドロビスフェノールAジグリシジルエーテルを主原料とする主剤が26容量部と、硬化剤としてたとえばアミン系硬化剤が9容量部とが混合機などに投入され、すばやく撹拌される。続いて、このように混合された合成樹脂結合剤原料に砥粒16としてたとえば粒度が#1000である溶融アルミナ(Al23)砥粒が20容量部と、平均粒径100μm程度の有機質バルーンが15容量部とが更に投入され、所定時間たとえば約10分間程度撹拌される。上記有機質バルーンは気孔22を形成する目的で投入される。
【0016】
本実施例の合成樹脂結合剤18の主原料には、硬化後の単体のガラス転移温度が115℃、硬化剤と混合した際の粘度が0.6Pa・s、硬化後の単体の曲げ弾性率が1.8GPaとなる水添ビスフェノールAが用いられている。ここで、水添ビスフェノールAとは、ビスフェノールAの有する二重結合に水素が添加された化合物であり、若干の二重結合が残存していてもよい。水添ビスフェノールAは上記のように、樹脂混合粘度(樹脂を硬化剤と混合した際の粘度)が1Pa・s以下で且つ硬化後の単体のガラス転移温度が100℃以上という条件で、硬化後の単体の曲げ弾性率を上述の如く2GPa以下に抑えることができるという特性を有している為、合成樹脂結合剤18の主原料に用いられることで、粒度が#800以上といった微細な砥粒12を用いたレジノイド研削砥石10であっても製造上の問題が発生せず、合成樹脂結合剤18が砥粒12に対して適度な保持力を有し、前述のように切れ刃26の好適な自生がおこなわれるレジノイド研削砥石10を提供することができる。すなわち、合成樹脂結合剤18の硬化後のガラス転移温度が100℃以上であれば、研削に際して研削液の温度変化によるレジノイド研削砥石10の研削性能のばらつきが発生せず、また、上記砥石原料を混合する工程において、混合される砥石原料の粘度が1Pa・s以下であれば、砥粒12との混合が十分に行われ、撹拌熱が発生するなどしてエポキシ樹脂の硬化が異常促進されるといった問題も生じない。
【0017】
前記工程により混合された調合物に、続いて、平均粒径1mm程度の発砲ポリスチレン樹脂(発泡倍率10倍)30容量部が投入された後、所定時間たとえば約5分間程度更に撹拌される。この発砲ポリスチレン樹脂は、砥石組織に気孔22よりも大径であってチップポケットとして機能する図示しない巨大な気孔を形成する為に機能するものである。このようにして調整された砥石原料は、続いて所定の金型に鋳込まれ、常温で24時間程度放置されることである程度硬化させられた後脱型され、更に、約160℃で3時間保持の本硬化処理が施されることにより、レジノイド研削砥石10として形成される。
【0018】
以下、本発明者が行った研削試験について説明する。先ず、上記工程により本発明の一実施例である実施例試料を作成し、続いて、合成樹脂結合剤18の主原料にビスフェノールAを用いた他は上記実施例試料と同様の原料及び工程により比較例試料を作成した。比較例試料の原料であるビスフェノールAは、硬化後の単体の曲げ弾性率が2.9GPa、硬化剤と混合した際の粘度が0.5Pa・s、硬化後の単体のガラス転移温度が105℃となるものを用いた。こうして作成された実施例試料および比較例試料の形状は何れも外径455(mmφ)×厚さ150(mm)×内径228.6(mmφ)であった。この実施例試料と比較例試料とを用いて、以下に示す試験条件で本発明の効果を検証する為の研削試験を行った。
【0019】
[試験条件]
研削盤:心なし研削盤
砥石周速度:2000m/min
被削材:S45C生材
被削材寸法:φ15×L100
研削方法:通し送り研削
被削材送り速度:5m/min
調整砥石:ラバー砥石(外径255mmφ、厚さ150mm、内径127mm)
【0020】
図3は、この実験におけるレジノイド研削砥石10と被削材20との相対位置関係を示す図であり、(a)は平面図、(b)は正面図である。研削試験では、図3(a)に示すように、実施例試料あるいは比較例試料のレジノイド研削砥石10と、これらの試料が研削により摩耗した際に補正を行う為の調整砥石30との間に、外径15(mmφ)×長さ100(mm)の円筒状の被削材20を、図3(a)に矢印で示す方向すなわちレジノイド研削砥石10の回転軸心方向に連続的に送り込んで研削を施した。ここで、調整砥石30は図3に示すように、その軸心をレジノイド研削砥石10の軸心方向から若干傾けた状態で用いた。被削材20に設けられた取代が10μmφの設定から加工を開始し、取代が5μmφになったところで、図3(b)に矢印で示す方向すなわち調整砥石30の外周面における被削材20と接する箇所の法線方向へ調整砥石30を5μm前進させて被削材20の取代を再び10μmφに戻す補正を繰り返し、被削材20の加工本数に対する研削盤主軸の消費電力値(kW)の変化と被削材20の被削面24の表面品位(μRz)の評価を行った。
【0021】
図4は、研削試験の結果得られた被削材20の加工本数に対する研削盤主軸の消費電力値の推移を示すグラフである。このグラフによれば、実施例試料であるレジノイド研削砥石10による研削では、比較例試料であるレジノイド研削砥石10による研削に比較して初期の消費電力値が約30%低く、被削材20の加工本数が増えるに連れて消費電力値が徐々に低下する傾向にある。これにより、実施例試料では、研削によって砥石が適度に摩耗していることがわかる。また、実施例試料のグラフで180本付近と450本付近で消費電力値が上昇しているが、これは被削材20の取代が5μmφになったので、調整砥石30を被削材20の方向へ5μm前進させて被削材20の取代を10μmφに戻す補正を行ったことによるものである。この補正により消費電力値は一旦ほぼ初期値に近い値にまで上昇しているが、加工本数が増えるに従って消費電力値が徐々に低下するという結果が得られた。一方、比較例試料であるレジノイド研削砥石10では、被削材20の加工本数が130本程度までは加工本数が増えるに連れて消費電力値が低下する傾向を示したが、この本数を超えると徐々に消費電力値が上昇していき、440本目の加工を終えた段階で被削材20の被削面24に光沢ムラが発生した為、研削を中止した。また、比較例試料では、研削を続けても被削材取代が減少しなかった為、補正は行わなかった。
【0022】
同様に、研削試験の結果得られた被削材20の加工本数に対する被削材20の被削面24の状態(十点平均粗さ)を以下に示す。
【0023】
加工本数 (本) 1 150 300 440 450 600
実施例試料による被削面(μRz) 0.32 0.30 0.29 ― 0.29 0.29
比較例試料による被削面(μRz) 0.35 0.33 0.32 0.30 ― ―
[備考]
比較例試料による研削試験では、440本目の加工を終えた段階で被削材の被削面に光沢ムラが発生した為、研削を中止した。
【0024】
この結果によれば、実施例試料であるレジノイド研削砥石10による研削では、研削の施された600本全ての被削材20の被削面24について光沢ムラ、ラセンマーク、傷などの問題がなく、所望の表面品位が得られたのに対し、比較例試料であるレジノイド研削砥石10による研削では、上述の如く440本目に被削材20の被削面24に光沢ムラが発生し、445本目まで様子をみたが、この光沢ムラは治まらなかった。
【0025】
以上の試験結果から、合成樹脂結合剤18の主原料として水添ビスフェノールAを用いることで、粒度が#800以上といった微細砥粒16を用いたレジノイド砥石10であっても、合成樹脂結合剤18が砥粒16に対して適度な保持力を有し、切れ刃26を自生させて良好な被削材20の表面品位を継続的に得られるレジノイド研削砥石10を提供できることが確かめられた。
【0026】
このように、本実施例によれば、合成樹脂結合剤18の主原料として用いられる水添ビスフェノールAは、硬化剤と混合した際の粘度が1Pa・s以下で且つ硬化後の単体のガラス転移温度が100℃以上の条件を満たすもので、硬化後の単体の曲げ弾性率が2GPa以下となるものが容易に得られる為、粒度が#800以上といった微細な砥粒16を用いたレジノイド研削砥石10であっても、合成樹脂結合剤18が砥粒16に対して適度な保持力を有し、切れ刃26を自生させて被削材20の良好な表面品位を継続的に得られるレジノイド研削砥石10を提供することができる。
【0027】
また、本実施例によれば、前記合成樹脂結合剤は、主剤と硬化剤と混合した際の粘度が1Pa・s以下となるものである為、レジノイド研削砥石10の製造において、合成樹脂結合剤18の主原料と硬化剤とを混合する際の粘度が十分に低い為に砥粒16との混合が好適に行われ、混合時の撹拌熱によりエポキシ樹脂の硬化を異常促進させるなどの製造上が問題が発生しない。
【0028】
また、本実施例によれば、前記合成樹脂結合剤は、硬化後の単体のガラス転移温度が100℃以上となるものである為、研削時に用いられる研削液の温度変化によってレジノイド研削砥石10の研削性能がばらつき易くなるなどの砥石の性能に関する問題が発生しない。
【0029】
また、本実施例によれば、前記合成樹脂結合剤は、硬化後の単体の曲げ弾性率が2GPa以下となるものである為、粒度が#800以上といった微細な砥粒16を用いたレジノイド研削砥石10であっても、合成樹脂結合剤18が砥粒16に対して適度な保持力を有し、切れ刃26を自生させて良好な被削材20の表面品位を継続的に得られるレジノイド研削砥石10を提供することができる。
【0030】
以上、本発明の一実施例を図面に基づいて詳細に説明したが、本発明は更に別の態様でも実施される。
【0031】
例えば、前述の実施例では、円筒研削型の円盤状砥石であるレジノイド研削砥石10について説明したが、本発明はこれに限定されず、合成樹脂結合剤18によって粒度が#800以上である砥粒16が相互に結合されて構成されたレジノイド研削砥石に広く用いられるものであり、たとえば、平面研削型の円盤状砥石や、カップ型砥石、内面研削砥石等の種々のレジノイド研削砥石に好適に用いられるものである。
【0032】
また、前述の実施例では、粒度が#1000程度のアルミナ(Al23)砥粒が用いられていたが、炭化ケイ素(SiC)砥粒、ジルコニア−アルミナ(ZrO2−Al23)系砥粒などの他の一般砥粒、立方晶窒化ホウ素(CBN)砥粒やダイヤモンド砥粒などの超砥粒、あるいはこれらの混合物が砥粒16として用いられたレジノイド研削砥石10にも本発明は同様に適用される。また、砥粒16の粒度は適宜変更される。
【0033】
また、前述の実施例においては、レジノイド研削砥石10の全体が、砥粒16が合成樹脂結合剤18によって結合された砥石組織から構成されていたが、合成樹脂や金属などから成るコア部の周囲に外周砥石部が設けられた研削砥石にも、本発明は同様に適用される。
【0034】
その他、一々例示はしないが、本発明はその主旨を逸脱しない範囲で種々の変更を加えて実施されるものである。
【図面の簡単な説明】
【図1】本発明の一実施例であるレジノイド研削砥石の形状を示す斜視図である。
【図2】本発明の一実施例であるレジノイド研削砥石の構成を拡大して示す図である。
【図3】本発明者がおこなった研削試験におけるレジノイド研削砥石と被削材との相対位置関係を示す図である。
【図4】本発明者がおこなった研削試験の結果得られた被削材の加工本数に対する研削盤主軸の消費電力値の推移を示すグラフである。
【符号の説明】
10:レジノイド研削砥石
16:砥粒
18:合成樹脂結合剤
[0001]
BACKGROUND OF THE INVENTION
In particular, the present invention relates to a resinoid grinding wheel composed of abrasive particles having a particle size of # 800 or more bonded to each other using a hydrogenated epoxy resin as a binder.
[0002]
[Prior art]
For example, a resinoid grinding wheel in which abrasive grains are bonded with a synthetic resin binder (resin bond) is generally used for grinding with a large machining allowance such as roughing. Resinoid grinding wheels are suitably used for such grinding because synthetic resin binders that bond abrasive grains are used for vitreous bond (vitrified bond), metallic binder (metal bond), electrodeposition bonding, etc. This is because the modulus of elasticity is lower than that of the workpiece, so that the load acting on the abrasive grains from the work material during grinding can be reduced by elastic deformation of the binder. In particular, resinoid grinding wheels using an epoxy resin as a binder have a lower elastic modulus than those using a phenol resin as a binder, and are long in the above-described work utilizing the characteristics. Widely used for processing thin pipes. Among resinoid grinding wheels using such epoxy resins as binders, the above characteristics can be most remarkably achieved by the method of casting a liquid epoxy resin and abrasive grains into a mold after mixing them. The resinoid grindstone is produced by a combination of a low elastic modulus, which is a characteristic of an epoxy resin, and a physically strong bond due to wetting of abrasive grains and a binder obtained by this casting method. It is thought to give excellent grinding performance.
[0003]
[Problems to be solved by the invention]
However, for the purpose of improving the quality of the work surface of the work material, in resinoid grinding wheels that use epoxy resin as a binder with fine abrasive grains with a particle size of # 800 or more, clogging and welding of chips on the grindstone processed surface Therefore, the surface quality of the desired work material cannot be continuously obtained and the dressing is frequently required due to reasons such as uneven gloss on the work surface of the work material, spiral marks and scratches. There was a problem.
[0004]
The present invention has been made to solve such a problem, and the object of the present invention is to use a synthetic resin binder even in a resinoid grinding wheel using fine abrasive grains having a particle size of # 800 or more. An object of the present invention is to provide a resinoid grinding wheel having an appropriate holding force for abrasive grains and capable of continuously obtaining a good work surface quality by generating a cutting edge by itself.
[0005]
[Means for solving the problems]
The present inventor continues to study the above problems, and regarding the resinoid grindstone using an epoxy resin using fine abrasive grains having a particle size of # 800 or more as a binder, it is the abrasive grains and the binder that cause the above problems. It came to the view that the bond with the epoxy resin was too strong for fine abrasive grains having a particle size of # 800, preventing the self-growth of the cutting edge. In other words, the work that uses resinoid grinding wheels using fine abrasive grains is generally smaller than the case of coarse grains, and the number of abrasive grains involved in grinding on the work surface of the work material As a result, the amount of fine abrasive grains will inevitably increase. As a result, the load on one abrasive grain will be reduced, so that the bonding force that holds the abrasive grains will be the same for fine abrasive grains and coarse grains. However, since the force to drop off the abrasive grains was relatively small, it was considered that the cutting edge was not moderately self-generated.
[0006]
By the way, it is generally considered that the bonding force of the abrasive grains by the epoxy resin is dominated by the physical caulking force. To reduce this, it is necessary to lower the elastic modulus of the epoxy resin alone. . In order to lower the elastic modulus of epoxy resin mainly composed of bisphenol A, which is generally used as a synthetic resin binder for resinoid grinding wheels, a reactive diluent must be added at the manufacturing stage. The addition of a functional diluent reduces not only the modulus of elasticity of the synthetic resin binder but also the heat resistance, so the grinding performance of the resinoid grinding wheel is likely to vary due to temperature changes in the grinding fluid used during grinding. In addition to new problems related to performance, in the production of resinoid grinding wheels, the viscosity when mixed with a curing agent is increased, so mixing with abrasive grains is not performed sufficiently. There is a possibility that manufacturing problems such as abnormally promoting the curing of the resin may occur. The resin mixing viscosity (viscosity when the resin is mixed with a curing agent) for obtaining a sufficiently mixed state with fine abrasive grains having a particle size of # 800 or more is generally 1 Pa · s or less. In order to suppress this, in order to satisfy the condition that the single glass transition temperature after curing is 100 ° C. or higher, a material such as bisphenol A has a minimum elastic modulus of 3 GPa after curing.
[0007]
The present invention has been made against the background of the above circumstances. The gist of the present invention is a resinoid grinding wheel composed of abrasive grains having a particle size of # 800 or more bonded together by a synthetic resin binder. a is, the synthetic resin binder, and wherein the hydrogenated bisphenol a all SANYO to use base resin as a main raw material, the glass transition temperature of a single post-curing is made of a 100 ° C. or higher To do.
[0008]
【The invention's effect】
In this way, the synthetic resin binder uses a main agent mainly composed of hydrogenated bisphenol A, and since the glass transition temperature of a simple substance after curing is 100 ° C. or higher, Even with resinoid grinding wheels that use fine abrasive grains with a grain size of # 800 or more, there are problems related to the performance of the grinding stone, such as the grinding performance of the resinoid grinding wheel tends to vary due to changes in the temperature of the grinding fluid used during grinding. Therefore, it is possible to provide a resinoid grinding wheel in which the synthetic resin binder has an appropriate holding force with respect to the abrasive grains, and the cutting edge is allowed to grow spontaneously to continuously obtain a good work surface quality.
[0009]
Other aspects of the invention
Here, preferably, the synthetic resin binder has a viscosity of 1 Pa · s or less when the main agent and the curing agent are mixed. In this way, in the production of the resinoid grinding wheel 10, since the viscosity when mixing the main raw material of the synthetic resin binder and the curing agent is sufficiently low, mixing with the abrasive grains is suitably performed. Manufacturing problems such as abnormally accelerating the curing of the epoxy resin due to the heat of stirring are not generated.
[0011]
Preferably, the synthetic resin binder has a flexural modulus of a simple substance after curing of 2 GPa or less. In this way, even if it is a resinoid grinding wheel using fine abrasive grains having a particle size of # 800 or more, the synthetic resin binder has an appropriate holding force for the abrasive grains, and the cutting edge is allowed to grow spontaneously. It is possible to provide a resinoid grinding wheel capable of continuously obtaining good work material surface quality.
[0012]
【Example】
Hereinafter, an embodiment of the present invention will be described in detail with reference to the drawings.
[0013]
FIG. 1 is a perspective view showing the shape of a resinoid grinding wheel 10 according to an embodiment of the present invention. In the figure, a resinoid grinding wheel 10 is a cylindrical grinding type disk-shaped grinding wheel which is integrally formed with dimensions of an outer diameter of 500 (mmφ) × thickness 150 (mm) × inner diameter of 200 (mmφ), for example. There is a mounting hole 12 provided in the central portion, which is attached to the main shaft of a grinding machine (not shown) and supplies a grinding liquid between the outer peripheral grinding surface 14 and the work material, and is held by a holding device (not shown). In a state where the cutting material is pressed against the outer peripheral grinding surface 14, it is rotated around its axis and used. As a result, the work surface of the work material is ground into the desired shape by the outer peripheral grinding surface 14.
[0014]
FIG. 2 is an enlarged view showing the configuration of the resinoid grinding wheel 10. In this figure, a resinoid grinding wheel 10 includes general abrasive grains such as SiC and fused alumina, and abrasive grains 16 which are superabrasive grains such as CBN and diamond, which are bonded to each other by a resin bond, that is, a synthetic resin binder 18. Thus, a large number of pores 22 are provided. In the resinoid grinding wheel 10 configured in this manner, the outer peripheral grinding surface 14 is brought into sliding contact with the work surface 24 of the work material 20 as described above, so that the cutting edges 26 of the abrasive grains 16 become the work material 20. The work surface 24 is ground. When a part of the abrasive grains 16 is crushed along with the grinding, the next cutting edge 26 is regenerated and the grinding performance is continued. The weight ratio of the synthetic resin binder 18 to the abrasive grains 16 or the whole is determined so as to exclusively and sufficiently bond the abrasive grains 16, and when the crushed abrasive grains 16 become small, the synthetic resin binder is used. Since the holding force of 18 is reduced, it is dropped together with the crushed abrasive grains 16 so that the next abrasive grains 16 are involved in grinding. At this time, the larger the number of the abrasive grains 16, that is, the smaller the particle diameter, the smaller the cutting edge 26 involved in the grinding and the more the number of cutting edges. Smooth surface quality of the workpiece can be obtained.
[0015]
The resinoid grinding wheel 10 of the present embodiment is manufactured as follows, for example. First, 26 parts by volume of a main ingredient mainly composed of hydrogenated bisphenol A such as hexahydrobisphenol A diglycidyl ether as the synthetic resin binder 18 and 9 parts by volume of an amine curing agent as a curing agent, for example, in a mixer Charged and stirred quickly. Subsequently, the synthetic resin binder raw material mixed in this manner has 20 parts by volume of fused alumina (Al 2 O 3 ) abrasive grains having a particle size of # 1000 as abrasive grains 16 and an organic balloon having an average particle diameter of about 100 μm. 15 parts by volume are further charged and stirred for a predetermined time, for example, about 10 minutes. The organic balloon is introduced for the purpose of forming pores 22.
[0016]
The main raw material of the synthetic resin binder 18 of this example includes a single glass transition temperature after curing of 115 ° C., a viscosity when mixed with a curing agent of 0.6 Pa · s, and a single bending elastic modulus after curing. Hydrogenated bisphenol A having a pressure of 1.8 GPa is used. Here, hydrogenated bisphenol A is a compound in which hydrogen is added to the double bond of bisphenol A, and some double bonds may remain. As described above, hydrogenated bisphenol A has a resin mixed viscosity (viscosity when the resin is mixed with a curing agent) of 1 Pa · s or less and a cured glass transition temperature of 100 ° C. or higher after curing. As described above, it has the characteristic that the flexural modulus of the single body can be suppressed to 2 GPa or less, so that it is used as the main raw material of the synthetic resin binder 18, so that fine abrasive grains with a grain size of # 800 or more are used. Even in the resinoid grinding wheel 10 using the No. 12, no problem in manufacturing occurs, the synthetic resin binder 18 has an appropriate holding force for the abrasive grains 12, and the cutting edge 26 is suitable as described above. It is possible to provide a resinoid grinding wheel 10 that is self-generated. That is, if the glass transition temperature after curing of the synthetic resin binder 18 is 100 ° C. or higher, there will be no variation in the grinding performance of the resinoid grinding wheel 10 due to the temperature change of the grinding fluid during grinding, and In the mixing step, when the viscosity of the grindstone raw material to be mixed is 1 Pa · s or less, mixing with the abrasive grains 12 is sufficiently performed, and the curing of the epoxy resin is abnormally accelerated by generating heat of stirring. Such a problem does not occur.
[0017]
Subsequently, 30 parts by volume of a foamed polystyrene resin (foaming ratio 10 times) having an average particle diameter of about 1 mm is added to the preparation mixed in the above step, and then further stirred for a predetermined time, for example, about 5 minutes. This foamed polystyrene resin functions to form huge pores (not shown) having a diameter larger than the pores 22 and functioning as chip pockets in the grindstone structure. The grindstone raw material thus adjusted is then cast into a predetermined mold, left to stand for about 24 hours at room temperature, cured to some extent, and then demolded, and further at about 160 ° C. for 3 hours. The resinous grinding wheel 10 is formed by performing the main curing treatment.
[0018]
Hereinafter, a grinding test performed by the present inventor will be described. First, an example sample which is an example of the present invention is prepared by the above steps, and subsequently, the same raw materials and steps as the above example samples are used except that bisphenol A is used as the main raw material of the synthetic resin binder 18. A comparative sample was prepared. Bisphenol A, which is a raw material for the comparative sample, has a flexural modulus of 2.9 GPa after curing, a viscosity of 0.5 Pa · s when mixed with a curing agent, and a glass transition temperature of 105 ° C. after curing. What was used. The shape of the example sample and the comparative example sample thus prepared was OD 455 (mmφ) × thickness 150 (mm) × inner diameter 228.6 (mmφ). A grinding test for verifying the effect of the present invention was performed under the test conditions shown below using the example sample and the comparative example sample.
[0019]
[Test conditions]
Grinding machine: Centerless grinder grinding wheel peripheral speed: 2000m / min
Work Material: S45C Raw Material Work Material Dimensions: φ15 × L100
Grinding method: Through feed grinding Work material feed speed: 5m / min
Adjustment whetstone: Rubber whetstone (outer diameter 255 mmφ, thickness 150 mm, inner diameter 127 mm)
[0020]
FIG. 3 is a diagram showing a relative positional relationship between the resinoid grinding wheel 10 and the work material 20 in this experiment, (a) is a plan view, and (b) is a front view. In the grinding test, as shown in FIG. 3A, between the resinoid grinding wheel 10 of the example sample or the comparative example sample and the adjusting wheel 30 for correcting when these samples are worn by grinding. The cylindrical workpiece 20 having an outer diameter of 15 (mmφ) × 100 (mm) in length is continuously fed in the direction indicated by the arrow in FIG. 3A, that is, in the direction of the rotational axis of the resinoid grinding wheel 10. Grinded. Here, as shown in FIG. 3, the adjusting grindstone 30 was used in a state where its axis was slightly inclined from the axial direction of the resinoid grinding grindstone 10. When the machining allowance provided on the work material 20 starts from the setting of 10 μmφ and the machining allowance becomes 5 μmφ, the work material 20 in the direction indicated by the arrow in FIG. Changes in the power consumption value (kW) of the grinding machine spindle relative to the number of workpieces 20 processed are repeated by moving the adjusting wheel 30 forward by 5 μm in the normal direction of the contact point and returning the machining allowance of the workpiece 20 to 10 μmφ again. The surface quality (μRz) of the work surface 24 of the work material 20 was evaluated.
[0021]
FIG. 4 is a graph showing the transition of the power consumption value of the grinding machine spindle with respect to the number of workpieces 20 obtained as a result of the grinding test. According to this graph, in the grinding with the resinoid grinding wheel 10 as an example sample, the initial power consumption value is about 30% lower than the grinding with the resinoid grinding wheel 10 as a comparative example sample. The power consumption value tends to gradually decrease as the number of processing increases. Thereby, in an example sample, it turns out that the grindstone is worn moderately by grinding. In the graph of the example sample, the power consumption value increases around 180 and 450. This is because the machining allowance of the work material 20 is 5 μmφ. This is because correction was made so that the machining allowance of the work material 20 was returned to 10 μmφ by advancing in the direction by 5 μm. As a result of this correction, the power consumption value once increased to a value almost close to the initial value, but the power consumption value gradually decreased as the number of machining operations increased. On the other hand, in the resinoid grinding wheel 10 which is a comparative example sample, the power consumption value tended to decrease as the number of workpieces 20 increased to about 130, but when this number was exceeded, The power consumption value gradually increased, and since the unevenness of gloss occurred on the work surface 24 of the work material 20 after finishing the 440th machining, the grinding was stopped. Moreover, in the comparative sample, the work material removal allowance did not decrease even when grinding was continued, and thus correction was not performed.
[0022]
Similarly, the state (ten-point average roughness) of the work surface 24 of the work material 20 with respect to the number of work pieces 20 obtained as a result of the grinding test is shown below.
[0023]
Number of processing (pieces) 1 150 300 440 450 600
Surface cut by sample (μRz) 0.32 0.30 0.29 ― 0.29 0.29
Machining surface by comparative sample (μRz) 0.35 0.33 0.32 0.30 ― ―
[Remarks]
In the grinding test using the comparative sample, since the unevenness of gloss occurred on the work surface of the work material after finishing the 440th work, the grinding was stopped.
[0024]
According to this result, in the grinding with the resinoid grinding wheel 10 as an example sample, there are no problems such as uneven gloss, spiral marks, scratches, etc. on the work surfaces 24 of all 600 work materials 20 that have been ground, While the desired surface quality was obtained, in the grinding with the resinoid grinding wheel 10 which is a comparative sample, as described above, the unevenness of gloss occurs on the work surface 24 of the work material 20 at the 440th and the state up to the 445th is shown. The gloss unevenness was not cured.
[0025]
From the above test results, by using hydrogenated bisphenol A as the main raw material of the synthetic resin binder 18, the synthetic resin binder 18 can be used even for the resinoid grindstone 10 using the fine abrasive grains 16 having a particle size of # 800 or more. It has been confirmed that the resinoid grinding wheel 10 that has an appropriate holding force with respect to the abrasive grains 16 and can continuously obtain good surface quality of the work material 20 by causing the cutting edges 26 to grow spontaneously can be provided.
[0026]
Thus, according to this example, hydrogenated bisphenol A used as the main raw material of the synthetic resin binder 18 has a viscosity of 1 Pa · s or less when mixed with a curing agent, and a single glass transition after curing. Resinoid grinding wheel using fine abrasive grains 16 with a grain size of # 800 or more because a material having a temperature satisfying a condition of 100 ° C. or more and having a flexural modulus of 2 GPa or less after curing can be easily obtained. Even if the synthetic resin binder 18 has a moderate holding power to the abrasive grains 16, the resinoid grinding can continuously obtain a good surface quality of the work material 20 by self-generating the cutting edge 26. A grindstone 10 can be provided.
[0027]
In addition, according to this example, the synthetic resin binder has a viscosity of 1 Pa · s or less when mixed with the main agent and the curing agent. Therefore, in the production of the resinoid grinding wheel 10, the synthetic resin binder is used. Since the viscosity at the time of mixing the 18 main raw materials and the curing agent is sufficiently low, the mixing with the abrasive grains 16 is suitably performed, and the curing of the epoxy resin is abnormally accelerated by the stirring heat at the time of mixing. There is no problem.
[0028]
Moreover, according to the present Example, since the synthetic resin binder has a single glass transition temperature after curing of 100 ° C. or higher, the resinous grinding wheel 10 has a temperature change of the grinding fluid used during grinding. There are no problems related to the performance of the grinding wheel, such as the grinding performance becoming more variable.
[0029]
In addition, according to the present example, the synthetic resin binder has a flexural modulus of 2 GPa or less after being cured, and therefore, resinoid grinding using fine abrasive grains 16 having a particle size of # 800 or more. Even with the grindstone 10, the synthetic resin binder 18 has an appropriate holding force with respect to the abrasive grains 16, and the resin blade 18 can continuously obtain a good surface quality of the work material 20 by generating the cutting edge 26 by itself. A grinding wheel 10 can be provided.
[0030]
As mentioned above, although one Example of this invention was described in detail based on drawing, this invention is implemented also in another aspect.
[0031]
For example, in the above-described embodiment, the resinoid grinding wheel 10 which is a cylindrical grinding type disk-shaped grinding wheel has been described. However, the present invention is not limited to this, and the abrasive grains having a particle size of # 800 or more by the synthetic resin binder 18. 16 is widely used for resinoid grinding wheels configured by being coupled to each other. For example, it is suitably used for various resinoid grinding wheels such as a surface grinding type disc-shaped grinding wheel, a cup-type grinding wheel, and an internal grinding wheel. It is what
[0032]
In the above-described embodiment, alumina (Al 2 O 3 ) abrasive grains having a particle size of about # 1000 were used, but silicon carbide (SiC) abrasive grains, zirconia-alumina (ZrO 2 —Al 2 O 3 ). The present invention also relates to a resinoid grinding wheel 10 in which other general abrasive grains such as system abrasive grains, superabrasive grains such as cubic boron nitride (CBN) abrasive grains and diamond abrasive grains, or a mixture thereof are used as the abrasive grains 16. Applies as well. Moreover, the particle size of the abrasive grains 16 is appropriately changed.
[0033]
In the above-described embodiment, the entire resinoid grinding wheel 10 is composed of a grindstone structure in which the abrasive grains 16 are bonded by the synthetic resin binder 18, but around the core portion made of synthetic resin, metal, or the like. The present invention is similarly applied to a grinding wheel provided with an outer peripheral grinding wheel portion.
[0034]
In addition, although not illustrated one by one, the present invention is implemented with various modifications without departing from the gist thereof.
[Brief description of the drawings]
FIG. 1 is a perspective view showing the shape of a resinoid grinding wheel according to an embodiment of the present invention.
FIG. 2 is an enlarged view showing a configuration of a resinoid grinding wheel according to an embodiment of the present invention.
FIG. 3 is a diagram showing a relative positional relationship between a resinoid grinding wheel and a work material in a grinding test performed by the present inventor.
FIG. 4 is a graph showing the transition of the power consumption value of the grinding machine spindle with respect to the number of workpieces obtained as a result of the grinding test conducted by the present inventor.
[Explanation of symbols]
10: Resinoid grinding wheel 16: Abrasive grain 18: Synthetic resin binder

Claims (3)

合成樹脂結合剤によって粒度が#800以上である砥粒が相互に結合されて構成されたレジノイド研削砥石であって、
前記合成樹脂結合剤は、水添ビスフェノールAを主原料とする主剤を使用するものであり、硬化後の単体のガラス転移温度が100℃以上となるものであることを特徴とするレジノイド研削砥石。
A resinoid grinding wheel constructed by combining abrasive grains having a particle size of # 800 or more with a synthetic resin binder,
The synthetic resin binder, resinoid grinding wheel, characterized in that the hydrogenated bisphenol A all SANYO to use base resin as a main raw material, the glass transition temperature of a single post-curing is made of a 100 ° C. or higher .
前記合成樹脂結合剤は、主剤と硬化剤とを混合した際の粘度が1Pa・s以下となるものである請求項1のレジノイド研削砥石。  The resinoid grinding wheel according to claim 1, wherein the synthetic resin binder has a viscosity of 1 Pa · s or less when the main agent and the curing agent are mixed. 前記合成樹脂結合剤は、硬化後の単体の曲げ弾性率が2GPa以下となるものである請求項1又は2のレジノイド研削砥石。The resinoid grinding wheel according to claim 1 or 2 , wherein the synthetic resin binder has a flexural modulus of a simple substance after curing of 2 GPa or less.
JP2001254232A 2001-08-24 2001-08-24 Resinoid grinding wheel using hydrogenated bisphenol A type epoxy resin Expired - Fee Related JP3795778B2 (en)

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