JP2000265160A - Abrasive for high-speed mirror surface polishing - Google Patents
Abrasive for high-speed mirror surface polishingInfo
- Publication number
- JP2000265160A JP2000265160A JP6631999A JP6631999A JP2000265160A JP 2000265160 A JP2000265160 A JP 2000265160A JP 6631999 A JP6631999 A JP 6631999A JP 6631999 A JP6631999 A JP 6631999A JP 2000265160 A JP2000265160 A JP 2000265160A
- Authority
- JP
- Japan
- Prior art keywords
- abrasive
- silicon carbide
- polishing
- fine particles
- minute particles
- 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
Links
- 238000005498 polishing Methods 0.000 title claims abstract description 85
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims abstract description 52
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 52
- 239000002245 particle Substances 0.000 claims abstract description 45
- 239000010419 fine particle Substances 0.000 claims description 56
- 238000002156 mixing Methods 0.000 claims description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 2
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 2
- GEIAQOFPUVMAGM-UHFFFAOYSA-N ZrO Inorganic materials [Zr]=O GEIAQOFPUVMAGM-UHFFFAOYSA-N 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 16
- 239000006061 abrasive grain Substances 0.000 abstract description 12
- 229910052710 silicon Inorganic materials 0.000 abstract description 7
- 239000010703 silicon Substances 0.000 abstract description 7
- -1 silane compound Chemical class 0.000 abstract description 4
- 239000000377 silicon dioxide Substances 0.000 abstract description 4
- 239000003082 abrasive agent Substances 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 2
- 229930195733 hydrocarbon Natural products 0.000 abstract description 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 229910000077 silane Inorganic materials 0.000 abstract description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 abstract 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 abstract 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 abstract 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 abstract 2
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract 1
- 235000010216 calcium carbonate Nutrition 0.000 abstract 1
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 abstract 1
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 abstract 1
- 229910052681 coesite Inorganic materials 0.000 abstract 1
- 229910052593 corundum Inorganic materials 0.000 abstract 1
- 229910052906 cristobalite Inorganic materials 0.000 abstract 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract 1
- 235000012239 silicon dioxide Nutrition 0.000 abstract 1
- 229910052682 stishovite Inorganic materials 0.000 abstract 1
- 229910052905 tridymite Inorganic materials 0.000 abstract 1
- 239000012808 vapor phase Substances 0.000 abstract 1
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 1
- 235000012431 wafers Nutrition 0.000 description 19
- 239000002002 slurry Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 230000003287 optical effect Effects 0.000 description 6
- 230000003746 surface roughness Effects 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 238000000227 grinding Methods 0.000 description 5
- 238000001308 synthesis method Methods 0.000 description 5
- 229910000420 cerium oxide Inorganic materials 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000005304 optical glass Substances 0.000 description 4
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- 239000010453 quartz Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229920003261 Durez Polymers 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910010293 ceramic material Inorganic materials 0.000 description 3
- 239000008119 colloidal silica Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 229910052594 sapphire Inorganic materials 0.000 description 3
- 239000010980 sapphire Substances 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 2
- 229910013641 LiNbO 3 Inorganic materials 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000010574 gas phase reaction Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 238000007781 pre-processing Methods 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000003746 solid phase reaction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Polishing Bodies And Polishing Tools (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、シリコンウエハ等
の半導体ウエハ、水晶、石英、サファイアなどの光学結
晶、光学レンズ等のガラス基材、磁気ディスク、各種金
属材料、各種セラミックス材料等の被研磨加工物を高速
度で鏡面研磨することが可能な高速鏡面研磨用研磨材に
関する。The present invention relates to polishing of semiconductor wafers such as silicon wafers, optical crystals such as quartz, quartz, and sapphire, glass substrates such as optical lenses, magnetic disks, various metal materials, and various ceramic materials. The present invention relates to an abrasive for high-speed mirror polishing capable of mirror-polishing a workpiece at a high speed.
【0002】[0002]
【従来の技術】従来、シリコンウエハ、GaAsウエハ
などの鏡面研磨には、例えば、コロイダルシリカやCe
O2 微粒子を用いた研磨用スラリーや研磨用砥石が使用
されていた。2. Description of the Related Art Conventionally, for mirror polishing of a silicon wafer, a GaAs wafer, or the like, for example, colloidal silica or Ce
Polishing slurries and polishing whetstones using O 2 fine particles have been used.
【0003】〔問題点〕しかしながら、これらの研磨材
料を用いて研磨すると、研磨速度が著しく低く、鏡面を
得るには長時間を要し、生産性が低いものであった。更
に、研磨速度が低いため、鏡面研磨の前加工処理とし
て、ラッピング加工や研削加工を行い、エッチング処理
により加工ダメージ層を除去した後に鏡面研磨をしなけ
ればならず、極めて生産性の悪い鏡面研磨プロセスであ
った。[Problems] However, when these polishing materials are used for polishing, the polishing rate is extremely low, a long time is required to obtain a mirror surface, and the productivity is low. In addition, since the polishing rate is low, lapping or grinding must be performed as a pre-processing for mirror polishing, and mirror polishing must be performed after removing the processing damage layer by etching, resulting in extremely low productivity. It was a process.
【0004】一方、研磨速度が高い研磨材として、粒径
がサブμm以上の炭化珪素粒子と、アルミナ粒子または
シリカ粒子を含む研磨材が知られているが、このような
砥粒を含有する研磨材を用いて被研磨加工物を研磨する
と、比較的高い研磨速度を達成できるものの、鏡面が得
られず、得られる研磨体の表面粗さ(Ra)はせいぜい
数十〜数百nm程度であった。なお、「表面粗さ(R
a)」とは、接触指針型表面粗さ計等で測定される、研
磨体表面における凸部と凹部の段差の平均(中心線平均
粗さ)をいうものとする。On the other hand, as an abrasive having a high polishing rate, an abrasive containing silicon carbide particles having a particle diameter of sub-μm or more and alumina particles or silica particles is known, and a polishing agent containing such abrasive grains is known. When the workpiece is polished using a material, a relatively high polishing rate can be achieved, but a mirror surface cannot be obtained, and the surface roughness (Ra) of the obtained polished body is at most about several tens to several hundreds of nm. Was. In addition, "surface roughness (R
"a)" refers to the average of the steps (center line average roughness) of the steps between the projections and the depressions on the surface of the polishing body, as measured by a contact pointer type surface roughness meter or the like.
【0005】[0005]
【発明が解決しようとする課題】本発明は、従来の技術
が有する上記問題点に鑑みなされたものであって、その
ために具体的に設定された課題は、研磨速度が著しく向
上し、短時間で鏡面が得られて生産性が向上した高速鏡
面研磨用研磨材を提供することにある。SUMMARY OF THE INVENTION The present invention has been made in view of the above-mentioned problems of the prior art, and the problems specifically set for that purpose are that the polishing rate is significantly improved, An object of the present invention is to provide an abrasive for high-speed mirror polishing in which a mirror surface is obtained by the above method and productivity is improved.
【0006】[0006]
【課題を解決するための手段】上記課題は、粒径 0.1μ
m以下の炭化珪素微粒子と、該炭化珪素微粒子以外の砥
粒微粒子とを少なくとも含有する研磨材により、解決す
ることができる。ここに、前記炭化珪素微粒子の配合割
合は、前記炭化珪素微粒子と前記炭化珪素微粒子以外の
砥粒微粒子との合量に対して、 0.1〜 60 重量%である
ことが好ましい。また、前記炭化珪素微粒子以外の砥粒
微粒子は、SiO2 、Al2 O3 、ZrO2 、Ce
O2 、Fe2 O3 、Fe3 O4 、Cr2 O3 、Mn
O2 、BaCO3、CaCO3 からなる群から選ばれた
少なくとも1種であることが好ましい。Means for Solving the Problems The above-mentioned object is attained with a particle size of 0.1 μm.
The problem can be solved by an abrasive containing at least m silicon carbide fine particles and abrasive fine particles other than the silicon carbide fine particles. Here, the mixing ratio of the silicon carbide fine particles is preferably 0.1 to 60% by weight based on the total amount of the silicon carbide fine particles and the abrasive fine particles other than the silicon carbide fine particles. The abrasive particles other than the silicon carbide particles include SiO 2 , Al 2 O 3 , ZrO 2 , Ce
O 2 , Fe 2 O 3 , Fe 3 O 4 , Cr 2 O 3 , Mn
It is preferably at least one selected from the group consisting of O 2 , BaCO 3 , and CaCO 3 .
【0007】[0007]
【発明の実施の形態】以下、本発明の実施の形態を具体
的に説明する。ただし、この実施の形態は、発明の趣旨
をより良く理解させるため具体的に説明するものであ
り、特に指定のない限り、発明内容を限定するものでは
ない。DESCRIPTION OF THE PREFERRED EMBODIMENTS Embodiments of the present invention will be specifically described below. However, this embodiment is specifically described for better understanding of the gist of the invention, and does not limit the content of the invention unless otherwise specified.
【0008】本実施の形態に係る研磨材は、砥粒とし
て、粒径 0.1μm以下の炭化珪素微粒子と、該炭化珪素
微粒子以外の砥粒微粒子とを少なくとも含有する。前記
炭化珪素微粒子は、どのような方法で製造されたもので
あっても良いが、例えば、非酸化性雰囲気のプラズマ中
にシラン化合物またはハロゲン化珪素と炭化水素とから
なる原料ガスを導入し、反応系の圧力を1気圧未満から
0.1 torr の範囲で制御しつつ気相反応させることによ
って製造されたもの(以下、「プラズマ気相合成法で得
られた炭化珪素微粒子」という)が、次に記す研磨メカ
ニズムが生起しやすく、球状、かつ微細であり、また高
純度である点で好適である。The abrasive according to the present embodiment contains, as abrasive grains, at least silicon carbide fine particles having a particle size of 0.1 μm or less and abrasive fine particles other than the silicon carbide fine particles. The silicon carbide fine particles may be produced by any method, for example, by introducing a raw material gas comprising a silane compound or silicon halide and a hydrocarbon into plasma in a non-oxidizing atmosphere, The pressure of the reaction system from less than 1 atmosphere
The one manufactured by performing a gas phase reaction while controlling within a range of 0.1 torr (hereinafter referred to as “silicon carbide fine particles obtained by plasma vapor synthesis”) is likely to have the polishing mechanism described below, and has a spherical shape. It is suitable in that it is fine and fine and has high purity.
【0009】本研磨材による被研磨加工物の研磨メカニ
ズムは、必ずしも明確でないが、粒径 0.1μm以下の炭
化珪素微粒子はその表面が非常に活性であり、被研磨加
工物との真実接触点で、両者の固相反応或いは被研磨加
工物表面の酸化反応が起こり、この生成層が炭化珪素微
粒子、及び炭化珪素微粒子以外の研磨微粒子により除去
されることにより、高い鏡面研磨速度が得られるものと
考えられる。即ち、微粒子炭化珪素砥粒の添加は、従来
の鏡面研磨用砥粒による研磨に研磨促進効果が付加され
ることにより、高速鏡面研磨が達成されるものと考えら
れる。Although the polishing mechanism of the workpiece to be polished by the present abrasive is not always clear, silicon carbide fine particles having a particle diameter of 0.1 μm or less have a very active surface, and the silicon carbide fine particles have a true contact point with the workpiece. A solid phase reaction between the two or an oxidation reaction on the surface of the workpiece to be polished occurs, and the resulting layer is removed by fine particles of silicon carbide and fine particles other than the fine particles of silicon carbide, so that a high mirror polishing rate can be obtained. Conceivable. That is, it is considered that the addition of the fine-grain silicon carbide abrasive grains achieves high-speed mirror polishing by adding a polishing promoting effect to the conventional polishing using the mirror polishing abrasive grains.
【0010】前記研磨材において、前記炭化珪素微粒子
の配合割合は、前記炭化珪素微粒子と前記炭化珪素微粒
子以外の砥粒微粒子との合量に対して、 0.1〜 60 重量
%であることが好ましい。前記炭化珪素微粒子の砥粒総
量に対する割合が 0.1重量%未満となると、本発明の目
的である高速鏡面研磨を達成することができず、また、
前記割合が 60 重量%を超えても鏡面研磨速度は向上し
ないのでコスト面で不利となる。[0010] In the above-mentioned abrasive, the compounding ratio of the silicon carbide fine particles is preferably 0.1 to 60% by weight based on the total amount of the silicon carbide fine particles and the abrasive fine particles other than the silicon carbide fine particles. When the ratio of the silicon carbide fine particles to the total amount of the abrasive grains is less than 0.1% by weight, the high-speed mirror polishing as the object of the present invention cannot be achieved,
If the ratio exceeds 60% by weight, the mirror polishing speed is not improved, so that it is disadvantageous in cost.
【0011】前記炭化珪素微粒子以外の砥粒微粒子は、
SiO2 、Al2 O3 、ZrO2 、CeO2 、Fe2 O
3 、Fe3 O4 、Cr2 O3 、MnO2 、BaCO3 、
CaCO3 からなる群から選ばれた少なくとも1種、特
にSiO2 、CeO2 、Fe 2 O3 、Cr2 O3 、Mn
O2 、BaCO3 、CaCO3 からなる群から選ばれた
少なくとも1種であることが、メカノケミカル鏡面研磨
が促進される点で好適である。また、前記炭化珪素微粒
子以外の砥粒微粒子の粒径は、特に限定されるものでは
なく、例えば、砥粒として通常用いられている程度のも
ので良い。The abrasive particles other than the silicon carbide particles are:
SiOTwo, AlTwoOThree, ZrOTwo, CeOTwo, FeTwoO
Three, FeThreeOFour, CrTwoOThree, MnOTwo, BaCOThree,
CaCOThreeAt least one selected from the group consisting of
SiOTwo, CeOTwo, Fe TwoOThree, CrTwoOThree, Mn
OTwo, BaCOThree, CaCOThreeSelected from the group consisting of
Mechanochemical mirror polishing to be at least one kind
This is preferable in that is promoted. In addition, the silicon carbide fine particles
The particle size of the abrasive particles other than the particles is not particularly limited.
No, for example, the degree that is usually used as an abrasive
So good.
【0012】前記研磨材を用いた代表的な研磨方法を例
示すると、前記研磨材を加えて分散させたスラリーやペ
ーストを研磨クロスと被研磨加工物との間に供給しつつ
回転させて湿式鏡面研磨を行う方法、或いは前記研磨材
を砥石状、テープ状に成形し、または発泡体中に固定さ
せた研磨体を被研磨加工物に接触させて鏡面研磨を行う
方法などがある。An example of a typical polishing method using the above-mentioned polishing material is as follows. A slurry or paste in which the above-mentioned polishing material is added and dispersed is supplied between a polishing cloth and a work to be polished and rotated to obtain a wet mirror surface. There is a method of performing polishing, a method of forming the polishing material into a grindstone or tape shape, or a method of performing mirror polishing by bringing a polishing body fixed in a foam into contact with a workpiece to be polished.
【0013】前記砥石状に成形するには、前記研磨材に
より砥石全体を成形する場合や砥石の被研磨加工物との
接触部を部分的に形成させる場合とがあり、また砥石に
も研磨材を結合材なしで固化させたもの(ボンドレス砥
石)と、レジノイドボンド等の結合剤を使用して固化し
成形させたもの(レジノイドボンド砥石)があり得る。
この砥石における砥粒率(砥石中に占める砥粒の容積比
率)は、特に限定されるものではなく、通常 5〜 95 容
量%程度で良い。In order to form the grinding stone, there are cases where the whole grinding stone is formed by the above-mentioned abrasive material and where the contact portion of the grinding stone with the workpiece to be polished is partially formed. Can be solidified without a binder (bondless grindstone), or solidified using a binder such as resinoid bond or the like (resinoid bond grindstone).
The abrasive grain ratio (volume ratio of the abrasive grains in the grindstone) of the grindstone is not particularly limited, and may be generally about 5 to 95% by volume.
【0014】レジノイドボンド砥石の形成に用いるレジ
ノイドボンドは、公知の熱硬化性樹脂、熱可塑性樹脂、
水溶性高分子樹脂などの単体または混合物を用いること
ができる。また、レジノイドボンド砥石またはボンドレ
ス砥石の成形は、一般に用いられる公知の成形技術を用
いて形成することができる。The resinoid bond used for forming the resinoid bond grindstone may be a known thermosetting resin, thermoplastic resin,
A simple substance such as a water-soluble polymer resin or a mixture thereof can be used. In addition, the resinoid bond grindstone or the bondless grindstone can be formed by using a generally used known molding technique.
【0015】一方、前記研磨材を加えて分散させたスラ
リー(研磨液)とするには、粒径 0.1μm以下の炭化珪
素微粒子を1次粒子程度近くまで解砕し分散させておく
のが好ましい。その場合、ポリカルボン酸系界面活性剤
などを併用するとよい。On the other hand, in order to obtain a slurry (polishing liquid) in which the abrasive is added and dispersed, it is preferable that silicon carbide fine particles having a particle size of 0.1 μm or less are crushed to near primary particles and dispersed. . In that case, a polycarboxylic acid-based surfactant or the like may be used in combination.
【0016】研磨液における砥粒量については、特に制
限されるものではないが、好ましい砥粒量としては 1〜
15 重量%程度である。この砥粒量が少なすぎると研磨
速度が低下しすぎて実用性に欠け、又、砥粒量が多すぎ
ると研磨加工に寄与しない砥粒が多くなり、研磨液コス
トが上昇して研磨加工コストの上昇を招くので好ましく
ない。The amount of abrasive grains in the polishing liquid is not particularly limited, but a preferred amount of abrasive grains is 1 to
It is about 15% by weight. If the amount of the abrasive particles is too small, the polishing rate will be too low, resulting in lack of practicality, and if the amount of the abrasive particles is too large, the number of abrasive particles not contributing to the polishing will increase, and the polishing liquid cost will increase, resulting in an increase in the polishing cost. Undesirably increases.
【0017】このような例示した研磨方法の場合、被研
磨加工物の種類に応じて、適切に酸やアルカリ成分を含
有させた溶液を、前記研磨体と被研磨加工物との間に滴
下して研磨すると効果的である。In the case of the polishing method exemplified above, a solution containing an acid or an alkali component is dropped between the polishing body and the workpiece to be polished, depending on the type of the workpiece. Polishing is effective.
【0018】このような実施の形態によれば、粒径 0.1
μm以下の炭化珪素微粒子と、該炭化珪素微粒子以外の
砥粒微粒子とからなる砥粒を研磨材として用いるため、
鏡面研磨中に被研磨加工物表面に加工ダメージを与える
ことなく高速鏡面研磨が可能となる。According to such an embodiment, a particle size of 0.1
μm or less silicon carbide fine particles, in order to use an abrasive composed of abrasive particles other than the silicon carbide fine particles as an abrasive,
High-speed mirror polishing can be performed without causing processing damage to the surface of the workpiece during mirror polishing.
【0019】このため、これらの研磨方法を実施するこ
とにより、従来の鏡面研磨材の性能、特に鏡面研磨速度
を大幅に向上させることができるので、ラッピング加工
や研削加工後、直ちに表面粗さ(Ra)が例えば1nm
程度の鏡面研磨加工が可能となり、シリコンウエハやG
aAsなどの半導体ウエハの他、水晶、LiNbO3、
サファイアなどの光学結晶、液晶、光学レンズ、ブラウ
ン管、フォトマスクなどのガラス基材、磁気ディスク、
各種金属材料、各種セラミックス材料などの被研磨加工
物を、高生産性と低コストとを両立させて鏡面研磨仕上
げをすることができる。Therefore, by performing these polishing methods, the performance of the conventional mirror-polished material, particularly the mirror-polishing speed, can be greatly improved. Ra) is, for example, 1 nm
Mirror polishing to the extent possible.
In addition to semiconductor wafers such as aAs, quartz, LiNbO 3 ,
Optical substrates such as sapphire, liquid crystal, optical lenses, cathode ray tubes, glass substrates such as photomasks, magnetic disks,
Mirror-polished workpieces to be polished, such as various metal materials and various ceramic materials, can be made compatible with high productivity and low cost.
【0020】[0020]
【実施例】〔実施例1〕コロイダルシリカを含むシリコ
ンウエハ1次ポリッシング用スラリー(フジミインコー
ポレーテッド(株)製) 100mlに、プラズマ気相合成
法で得られた炭化珪素微粒子(住友大阪セメント(株)
製、粒径 0.05 μm以下、平均粒径 30nm)を水 1900
mlに分散させた分散液を添加・混合し、超音波を用
いて分散させ、研磨用スラリー(総砥粒含有量 5重量
%、総砥粒量に対する炭化珪素微粒子量 10 重量%)と
した。この研磨用スラリーを使用して表1に示した研磨
条件でラップドSiウエハを研磨した(研磨時間 30
分)。その結果を表3に示した。なお、表面粗さ(R
a)は接触指針型表面粗さ計により測定した。EXAMPLES Example 1 Silicon carbide fine particles (Sumitomo Osaka Cement Co., Ltd.) obtained by a plasma gas phase synthesis method were used in 100 ml of a slurry for primary polishing of silicon wafers containing colloidal silica (manufactured by Fujimi Incorporated). )
Made with water 1900
The resulting dispersion was added and mixed to obtain a polishing slurry (total abrasive content: 5% by weight, silicon carbide fine particles: 10% by weight based on the total amount of abrasives). Using this polishing slurry, a wrapped Si wafer was polished under the polishing conditions shown in Table 1 (polishing time 30
Minutes). Table 3 shows the results. The surface roughness (R
a) was measured by a contact pointer type surface roughness meter.
【0021】〔実施例2〕プラズマ気相合成法で得られ
た炭化珪素微粒子の総砥粒含有量に対する割合を20 重
量%とした他は実施例1に準じてラップドSiウエハを
研磨した。その結果を表3に示した。Example 2 A wrapped Si wafer was polished in the same manner as in Example 1 except that the ratio of the silicon carbide fine particles obtained by the plasma vapor synthesis method to the total abrasive content was 20% by weight. Table 3 shows the results.
【0022】〔実施例3〕酸化セリウム微粒子(信越化
学工業(株)製、平均粒径 100nm)を 10 重量%分散
させた水分散液 100mlに、プラズマ気相合成法で得ら
れた炭化珪素微粒子(住友大阪セメント(株)製、粒径
0.05 μm以下、平均粒径 30 nm)を水1900 ml分
散させた分散液を添加・混合し、超音波を用いて分散さ
せ、研磨用スラリー(総砥粒含有量 5重量%、総砥粒量
に対する炭化珪素微粒子量 20 重量%)とした。この研
磨用スラリーを使用して表1に示した研磨条件で光学ガ
ラスBK−7を研磨した。その結果を表3に示した。Example 3 Silicon carbide fine particles obtained by plasma gas phase synthesis in 100 ml of an aqueous dispersion in which 10% by weight of cerium oxide fine particles (manufactured by Shin-Etsu Chemical Co., Ltd., average particle size: 100 nm) were dispersed. (Sumitomo Osaka Cement Co., Ltd., particle size
A dispersion in which 1900 ml of water in which 0.05 μm or less and an average particle size of 30 nm are dispersed is added and mixed, and the mixture is dispersed using ultrasonic waves. The slurry for polishing (total abrasive content: 5% by weight, total abrasive amount) 20% by weight of silicon carbide fine particles based on Using this polishing slurry, the optical glass BK-7 was polished under the polishing conditions shown in Table 1. Table 3 shows the results.
【0023】〔実施例4〕シリカパウダー(日本アエロ
ジル(株)製、平均粒径 30 nm) 855g、プラズマ気
相合成法で得られた炭化珪素微粒子(住友大阪セメント
(株)製、粒径 0.05 μm以下、平均粒径 30 nm) 9
5 g、フェノール樹脂(住友デュレズ(株)製) 50 g
を混合し、砥石を成形した(総砥粒量に対する炭化珪素
微粒子量 10 重量%)。この砥石を用い、表2に示した
研磨条件でラップドSiウエハの研磨を 30 分間行い、
その結果を表3に示した。Example 4 855 g of silica powder (manufactured by Nippon Aerosil Co., Ltd., average particle size: 30 nm) and silicon carbide fine particles obtained by plasma vapor synthesis (manufactured by Sumitomo Osaka Cement Co., Ltd., particle size: 0.05 μm or less, average particle size 30 nm) 9
5 g, phenolic resin (Sumitomo Durez Co., Ltd.) 50 g
Was mixed to form a grindstone (amount of silicon carbide particles was 10% by weight based on the total amount of abrasive grains). Using this grindstone, polishing of the wrapped Si wafer was performed for 30 minutes under the polishing conditions shown in Table 2,
Table 3 shows the results.
【0024】〔実施例5〕プラズマ気相合成法で得られ
た炭化珪素微粒子の総砥粒含有量に対する割合を30 重
量%とした他は実施例4に準じてラップドSiウエハの
研磨を行い、表3にその結果を示した。Example 5 A lapped Si wafer was polished in the same manner as in Example 4 except that the ratio of the silicon carbide fine particles obtained by the plasma vapor synthesis method to the total abrasive content was 30% by weight. Table 3 shows the results.
【0025】〔実施例6〕シリカパウダーを酸化セリウ
ム微粒子(信越化学工業(株)製、平均粒径 100nm)
に変更した他は実施例4に準じて砥石を成形した。この
砥石を用い実施例4に準じて光学ガラスBK−7の研磨
を行い、表3に結果を示した。Example 6 Silica powder was converted to cerium oxide fine particles (Shin-Etsu Chemical Co., Ltd., average particle size 100 nm).
A whetstone was formed in the same manner as in Example 4 except for changing to. Using this grindstone, the optical glass BK-7 was polished according to Example 4, and the results are shown in Table 3.
【0026】〔比較例1〕コロイダルシリカを含むシリ
コンウエハ1次ポリッシング用スラリー(フジミインコ
ーポレーテッド(株)製)を用いた他は、実施例1に準
じて、ラップドSiウエハを研磨した。その結果を表3
に示した。Comparative Example 1 A wrapped Si wafer was polished in the same manner as in Example 1, except that a slurry for primary polishing of a silicon wafer containing colloidal silica (manufactured by Fujimi Incorporated) was used. Table 3 shows the results.
It was shown to.
【0027】〔比較例2〕シリカパウダー(日本アエロ
ジル(株)製、平均粒径 30 nm) 875g、フェノール
樹脂(住友デリュレズ(株)製) 50 gを混合し、砥石
を成形した。実施例1に準じて、ラップドSiウエハを
研磨した。その結果を表3に示した。Comparative Example 2 875 g of silica powder (manufactured by Nippon Aerosil Co., Ltd., average particle size: 30 nm) and 50 g of phenol resin (manufactured by Sumitomo Dellurez Co., Ltd.) were mixed to form a grindstone. In accordance with Example 1, the wrapped Si wafer was polished. Table 3 shows the results.
【0028】〔比較例3〕粒径 0.3μmの炭化珪素微粒
子(イビデン(株)製)を用いた他は、実施例1に準
て、ラップドSiウエハを研磨した。その結果を表3に
示した。Comparative Example 3 A wrapped Si wafer was polished in the same manner as in Example 1 except that silicon carbide fine particles having a particle size of 0.3 μm (manufactured by Ibiden Co., Ltd.) were used. Table 3 shows the results.
【0029】〔比較例4〕粒径 0.3μmの炭化珪素微粒
子(イビデン(株)製)を用いた他は、実施例4に準じ
て、砥石を成形した。実施例4に準じてラップドSiウ
エハを研磨した。その結果を表3に示した。Comparative Example 4 A grindstone was formed in the same manner as in Example 4 except that silicon carbide fine particles having a particle diameter of 0.3 μm (manufactured by IBIDEN Co., Ltd.) were used. A wrapped Si wafer was polished according to Example 4. Table 3 shows the results.
【0030】〔比較例5〕酸化セリウム(信越化学工業
(株)製、平均粒径 100nm) 50 gを水 950gに添加・
混合し、超音波を用いて分散させ、研摩スラリー(砥粒
含有量 5重量%)とした。この研摩用スラリーを使用し
て表1に示した研磨条件で光学ガラスBK−7を研磨し
た。その結果を表3に示した。Comparative Example 5 50 g of cerium oxide (manufactured by Shin-Etsu Chemical Co., Ltd., average particle size 100 nm) was added to 950 g of water.
The mixture was mixed and dispersed using ultrasonic waves to obtain a polishing slurry (abrasive content: 5% by weight). Using this polishing slurry, the optical glass BK-7 was polished under the polishing conditions shown in Table 1. Table 3 shows the results.
【0031】〔比較例6〕酸化セリウム(信越化学工業
(株)製、平均粒径 100nm) 950g、フェノール樹脂
(住友デュレズ(株)製) 50 gを混合し、砥石を成形
した。この砥石を用い、表2に示した研磨条件で光学ガ
ラスBK−7の研磨を 30 分間行い、その結果を表3に
示した。Comparative Example 6 950 g of cerium oxide (manufactured by Shin-Etsu Chemical Co., Ltd., average particle size 100 nm) and 50 g of phenol resin (manufactured by Sumitomo Durez Co., Ltd.) were mixed to form a grindstone. Using this grindstone, polishing of the optical glass BK-7 was performed for 30 minutes under the polishing conditions shown in Table 2, and the results are shown in Table 3.
【0032】〔比較例7〕プラズマ気相合成法で得られ
た炭化珪素微粒子(住友大阪セメント(株)製、粒径
0.05 μm以下、平均粒径 30 nm) 50 gを水 950g
に添加・混合し、超音波を用いて分散させ、研摩スラリ
ー(砥粒含有量 5重量%)とした。この研摩用スラリー
を使用して表1に示した研磨条件でラップドSiウエハ
を研磨した。その結果を表3に示した。[Comparative Example 7] Silicon carbide fine particles obtained by a plasma gas phase synthesis method (manufactured by Sumitomo Osaka Cement Co., Ltd., particle size
0.05 μm or less, average particle size 30 nm) 50 g to water 950 g
Was added to and mixed with the mixture, and dispersed using ultrasonic waves to obtain a polishing slurry (abrasive content: 5% by weight). Using this polishing slurry, a wrapped Si wafer was polished under the polishing conditions shown in Table 1. Table 3 shows the results.
【0033】〔比較例8〕プラズマ気相合成法で得られ
た炭化珪素微粒子(住友大阪セメント(株)製、粒径
0.05 μm以下、平均粒径 30 nm) 950g、フェノー
ル樹脂(住友デュレズ(株)製) 50 gを混合し、砥石
を成形した。この砥石を用い、表2に示した研磨条件で
ラップドSiウエハの研磨を 30 分間行い、その結果を
表3に示した。[Comparative Example 8] Silicon carbide fine particles obtained by a plasma gas phase synthesis method (manufactured by Sumitomo Osaka Cement Co., Ltd., particle size
950 g of 0.05 μm or less, average particle size of 30 nm) and 50 g of phenol resin (manufactured by Sumitomo Durez Co., Ltd.) were mixed to form a grindstone. Using this grindstone, polishing of the wrapped Si wafer was performed for 30 minutes under the polishing conditions shown in Table 2, and the results are shown in Table 3.
【0034】[0034]
【表1】 [Table 1]
【0035】[0035]
【表2】 [Table 2]
【0036】[0036]
【表3】 [Table 3]
【0037】[0037]
【発明の効果】以上のように本発明によれば、請求項1
に係る高速鏡面研磨用研磨材では、粒径 0.1μm以下の
炭化珪素微粒子と該炭化珪素微粒子以外の砥粒微粒子と
を少なくとも含有するように研磨材を構成したことによ
り、従来の鏡面研磨材の性能、特に鏡面研磨速度を大幅
に向上させることができるので、ラッピング加工や研削
加工後、直ちに表面粗さ(Ra)が例えば 1.0nm程度
の鏡面研磨加工が可能となり、シリコンウエハやGaA
sなどの半導体ウエハの他、水晶、LiNbO3、サフ
ァイアなどの光学結晶、液晶、光学レンズ、ブラウン
管、フォトマスクなどのガラス基材、磁気ディスク、各
種金属材料、各種セラミックス材料などの被研磨加工物
を、高生産性と低コストを両立させて鏡面研磨仕上げ加
工をすることができる。According to the present invention as described above, claim 1
In the abrasive for high-speed mirror polishing according to the present invention, the abrasive is configured to contain at least silicon carbide fine particles having a particle diameter of 0.1 μm or less and abrasive fine particles other than the silicon carbide fine particles, the conventional mirror-polished abrasive Since the performance, especially the mirror polishing speed, can be greatly improved, the mirror polishing with a surface roughness (Ra) of, for example, about 1.0 nm can be performed immediately after the lapping or grinding, and the silicon wafer or GaAs can be formed.
In addition to semiconductor wafers such as s, optical crystals such as quartz, LiNbO 3 , sapphire, glass substrates such as liquid crystals, optical lenses, cathode ray tubes and photomasks, magnetic disks, various metal materials, and various polished workpieces such as various ceramic materials Can be mirror-polished while achieving both high productivity and low cost.
【0038】また、請求項2に係る高速鏡面研磨用研磨
材では、前記炭化珪素微粒子の配合割合は、前記炭化珪
素微粒子と前記炭化珪素微粒子以外の砥粒微粒子との合
量に対して、 0.1〜 60 重量%であることにより、効率
良く高速に鏡面研磨できて、生産性が向上する。In the abrasive for high-speed mirror polishing according to claim 2, the mixing ratio of the silicon carbide fine particles is 0.1% with respect to the total amount of the silicon carbide fine particles and the abrasive fine particles other than the silicon carbide fine particles. When the content is up to 60% by weight, mirror polishing can be efficiently performed at high speed, and productivity is improved.
【0039】また、請求項3に係る高速鏡面研磨用研磨
材では、前記炭化珪素微粒子以外の砥粒微粒子が、Si
O2 、Al2 O3 、ZrO2 、CeO2 、Fe2 O3 、
Fe 3 O4 、Cr2 O3 、MnO2 、BaCO3 、Ca
CO3 からなる群から選ばれた少なくとも1種であるこ
とから、メカノケミカル鏡面研磨による高速な鏡面研磨
ができる。The polishing for high-speed mirror polishing according to the third aspect.
In the material, abrasive particles other than the silicon carbide particles are Si
OTwo, AlTwoOThree, ZrOTwo, CeOTwo, FeTwoOThree,
Fe ThreeOFour, CrTwoOThree, MnOTwo, BaCOThree, Ca
COThreeAt least one member selected from the group consisting of
High-speed mirror polishing by mechanochemical mirror polishing
Can be.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) H01L 21/304 622 H01L 21/304 622B (72)発明者 山本 良貴 千葉県船橋市豊富町585番地 住友大阪セ メント株式会社新規技術研究所内 Fターム(参考) 3C063 AA01 AB01 BB01 BB04 BB07 BB19 BC02 BC03 EE10 FF23──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification FI FI Theme Court ゛ (Reference) H01L 21/304 622 H01L 21/304 622B (72) Inventor Yoshiki Yamamoto 585 Tomicho, Funabashi-shi, Chiba Prefecture Sumitomo Osaka F-term in Cement Corporation New Technology Research Laboratory (reference) 3C063 AA01 AB01 BB01 BB04 BB07 BB19 BC02 BC03 EE10 FF23
Claims (3)
炭化珪素微粒子以外の砥粒微粒子とを少なくとも含有す
ることを特徴とする高速鏡面研磨用研磨材。An abrasive for high-speed mirror polishing, comprising at least silicon carbide fine particles having a particle size of 0.1 μm or less and abrasive fine particles other than the silicon carbide fine particles.
化珪素微粒子と前記炭化珪素微粒子以外の砥粒微粒子と
の合量に対して、 0.1〜 60 重量%である請求項1記載
の高速鏡面研磨用研磨材。2. The high-speed mirror surface according to claim 1, wherein the mixing ratio of said silicon carbide fine particles is 0.1 to 60% by weight based on the total amount of said silicon carbide fine particles and said abrasive fine particles other than said silicon carbide fine particles. Abrasive for polishing.
SiO2 、Al2 O3 、ZrO2 、CeO2 、Fe2 O
3 、Fe3 O4 、Cr2 O3 、MnO2 、BaCO3 、
CaCO3 からなる群から選ばれた少なくとも1種であ
ることを特徴とする請求項1または2記載の高速鏡面研
磨用研磨材。3. The abrasive fine particles other than the silicon carbide fine particles,
SiO 2 , Al 2 O 3 , ZrO 2 , CeO 2 , Fe 2 O
3 , Fe 3 O 4 , Cr 2 O 3 , MnO 2 , BaCO 3 ,
3. The abrasive for high-speed mirror polishing according to claim 1, wherein the abrasive is at least one member selected from the group consisting of CaCO 3 .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6631999A JP2000265160A (en) | 1999-03-12 | 1999-03-12 | Abrasive for high-speed mirror surface polishing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6631999A JP2000265160A (en) | 1999-03-12 | 1999-03-12 | Abrasive for high-speed mirror surface polishing |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2000265160A true JP2000265160A (en) | 2000-09-26 |
Family
ID=13312408
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6631999A Pending JP2000265160A (en) | 1999-03-12 | 1999-03-12 | Abrasive for high-speed mirror surface polishing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000265160A (en) |
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| WO2002072726A1 (en) * | 2001-03-09 | 2002-09-19 | Mitsui Mining & Smelting Co., Ltd. | Cerium based abrasive material and abrasive material slurry, and method for producing cerium based abrasive material |
| WO2009107567A1 (en) * | 2008-02-27 | 2009-09-03 | 住友電気工業株式会社 | Method for machining nitride semiconductor wafer, nitride semiconductor wafer, process for producing nitride semiconductor device, and nitride semiconductor device |
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| CN103498158A (en) * | 2013-09-23 | 2014-01-08 | 无锡阳工机械制造有限公司 | Polishing slurry |
| CN103498159A (en) * | 2013-09-23 | 2014-01-08 | 无锡阳工机械制造有限公司 | Polishing slurry |
| JP2015147922A (en) * | 2014-11-26 | 2015-08-20 | アサヒ化成工業株式会社 | Composite abrasive, manufacturing method thereof, polishing method and polishing apparatus |
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| CN112226205A (en) * | 2020-09-29 | 2021-01-15 | 江西庞泰环保股份有限公司 | Preparation method of mechanical grinding slurry |
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| US6946009B2 (en) | 2001-03-09 | 2005-09-20 | Mitsui Mining & Smelting Co., Ltd. | Cerium-based abrasive material and abrasive material slurry, and method for producing cerium based abrasive material |
| CN100376652C (en) * | 2001-03-09 | 2008-03-26 | 三井金属鉱业株式会社 | Cerium-based abrasive, abrasive slurry, and method for producing cerium-based abrasive |
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| JP2009231814A (en) * | 2008-02-27 | 2009-10-08 | Sumitomo Electric Ind Ltd | Method for machining nitride semiconductor wafer |
| JP2009231833A (en) * | 2008-02-27 | 2009-10-08 | Sumitomo Electric Ind Ltd | Nitride semiconductor wafer |
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