JP2003094323A - Retainer material of polishing object - Google Patents
Retainer material of polishing objectInfo
- Publication number
- JP2003094323A JP2003094323A JP2001290689A JP2001290689A JP2003094323A JP 2003094323 A JP2003094323 A JP 2003094323A JP 2001290689 A JP2001290689 A JP 2001290689A JP 2001290689 A JP2001290689 A JP 2001290689A JP 2003094323 A JP2003094323 A JP 2003094323A
- Authority
- JP
- Japan
- Prior art keywords
- holding material
- polished
- retainer material
- bubbles
- polishing
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 61
- 238000005498 polishing Methods 0.000 title claims abstract description 17
- 239000004094 surface-active agent Substances 0.000 claims abstract description 20
- 238000007711 solidification Methods 0.000 abstract description 3
- 230000008023 solidification Effects 0.000 abstract description 3
- 239000006185 dispersion Substances 0.000 abstract description 2
- 239000003381 stabilizer Substances 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 26
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 22
- 239000006260 foam Substances 0.000 description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 19
- 239000000203 mixture Substances 0.000 description 12
- -1 polyethylene adipate Polymers 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000011521 glass Substances 0.000 description 11
- 230000015271 coagulation Effects 0.000 description 8
- 238000005345 coagulation Methods 0.000 description 8
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 8
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 239000011259 mixed solution Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- 150000003077 polyols Chemical class 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000011342 resin composition Substances 0.000 description 4
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000004970 Chain extender Substances 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 210000000497 foam cell Anatomy 0.000 description 2
- IYWCBYFJFZCCGV-UHFFFAOYSA-N formamide;hydrate Chemical compound O.NC=O IYWCBYFJFZCCGV-UHFFFAOYSA-N 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- QUANRIQJNFHVEU-UHFFFAOYSA-N oxirane;propane-1,2,3-triol Chemical compound C1CO1.OCC(O)CO QUANRIQJNFHVEU-UHFFFAOYSA-N 0.000 description 2
- 229920000909 polytetrahydrofuran Polymers 0.000 description 2
- 229920003225 polyurethane elastomer Polymers 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 229920001342 Bakelite® Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006061 abrasive grain Substances 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229940093499 ethyl acetate Drugs 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000009191 jumping Effects 0.000 description 1
- 150000002596 lactones Chemical group 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000921 polyethylene adipate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、LCDガラス用、
カラーフィルター、セラミック基板、反射鏡、水晶発振
子、半導体ウエハー等の被研磨部材の保持材に関するも
のである。TECHNICAL FIELD The present invention relates to an LCD glass,
The present invention relates to a holding material for a member to be polished such as a color filter, a ceramic substrate, a reflecting mirror, a crystal oscillator, and a semiconductor wafer.
【0002】[0002]
【従来の技術】一般的に、LCDガラス用、カラーフィ
ルター、セラミック基板、反射鏡、水晶発振子、半導体
ウエハー等の被研磨部材は回転加工装置等の研磨機によ
り研磨加工される。その場合、被研磨部材を研磨機の定
盤に固定し、そして、この定盤と対向して配置された定
盤に研磨布を相対的に回転されると共に、両者間に砥粒
等を含む研磨液を供給する事によって、被研磨部材を研
磨する。2. Description of the Related Art Generally, a member to be polished such as a color filter for LCD glass, a ceramic substrate, a reflecting mirror, a crystal oscillator, and a semiconductor wafer is polished by a polishing machine such as a rotating machine. In that case, the member to be polished is fixed to the surface plate of the polishing machine, and the polishing cloth is relatively rotated on the surface plate arranged so as to face the surface plate, and an abrasive grain or the like is contained between them. The member to be polished is polished by supplying the polishing liquid.
【0003】この際の、被研磨部材の保持方法として
は、被研磨部材を保持するために適した高分子弾性発泡
体が用いられる。保持部材は被研磨部材が水等の液体を
介して強く押しつけられることにより被研磨部材に吸着
して該研磨部材を固定する。At this time, as a method for holding the member to be polished, a polymeric elastic foam suitable for holding the member to be polished is used. When the member to be polished is strongly pressed through a liquid such as water, the holding member adsorbs to the member to be polished and fixes the member to be polished.
【0004】また、研磨加工中に被研磨部材が定盤から
の飛び出すのを防止するために、特開昭61−2308
66のような被研磨部材を嵌合するリセス孔を有するテ
ンプレートを設ける方法も採用されている。Further, in order to prevent the member to be polished from jumping out of the surface plate during the polishing process, JP-A-61-2308.
A method of providing a template such as 66 having a recess hole into which a member to be polished is fitted is also adopted.
【0005】これらの方法で用いられる保持材は、一般
にウレタン樹脂組成物を用いた湿式凝固で製造される。
この湿式凝固法は、ウレタン樹脂組成物を調整した後ウ
レタン樹脂組成物を支持体に塗布し、次いで、水、ジメ
チルホルムアミド(DMF)混合溶液中にて湿式凝固処
理を行い、支持体上に発泡層を生成させ、その後乾燥し
場合によっては最表面をバフして保持材を得るものであ
る。The holding material used in these methods is generally produced by wet coagulation using a urethane resin composition.
In this wet coagulation method, after the urethane resin composition is prepared, the urethane resin composition is applied to a support, and then wet coagulation treatment is performed in a mixed solution of water and dimethylformamide (DMF) to foam on the support. A layer is formed and then dried, and in some cases, the outermost surface is buffed to obtain a holding material.
【0006】また、特開2000−42909のよう
に、支持体と湿式発泡層の間に、支持体の組成と湿式発
泡層の組成を含む熱可塑性樹脂層を積層することによ
り、剥離強力の強い保持材を得ることができる。Further, as in JP-A-2000-42909, by laminating a thermoplastic resin layer containing the composition of the support and the composition of the wet foam layer between the support and the wet foam layer, the peel strength is strong. A holding material can be obtained.
【0007】[0007]
【発明が解決しようとする課題】このような保持材は、
湿式凝固処理により、支持体上に発泡層を形成する際、
発泡層中の発泡セルを均一な大きさに揃えるために、ウ
レタン樹脂組成物、水、ジメチルホルムアミド(DM
F)混合溶液中に、各種界面活性剤等の分散安定剤及び
湿式凝固助剤を添加する。この添加剤が発泡層に残存す
ることで、被研磨部材の研磨において泡が発生し、被研
磨部材の品質低下、製品の歩留まりを悪化させる。Such a holding material is
When forming the foam layer on the support by the wet coagulation treatment,
In order to make the foam cells in the foam layer uniform in size, a urethane resin composition, water, dimethylformamide (DM
F) A dispersion stabilizer such as various surfactants and a wet coagulation aid are added to the mixed solution. When this additive remains in the foam layer, bubbles are generated during polishing of the member to be polished, which deteriorates the quality of the member to be polished and deteriorates the yield of products.
【0008】[0008]
【課題を解決するための手段】本発明は、上述の課題を
解決するために、研磨中に発生する泡の量が少量である
被研磨部材の保持材を提供するものである。SUMMARY OF THE INVENTION In order to solve the above problems, the present invention provides a holding material for a member to be polished in which the amount of bubbles generated during polishing is small.
【0009】すなわち、保持材に含有される界面活性剤
の量が、5.0mg/g保持材以下である被研磨部材の
保持材または、研磨中に保持材から発生する泡が5個/
5400mm2以下であることを特徴とする被研磨部材
の保持材により課題を解決しうる。That is, the amount of the surfactant contained in the holding material is 5.0 mg / g or less, and the holding material of the member to be polished or the bubbles generated from the holding material during polishing is 5 /
The problem can be solved by the holding material for the member to be polished, which is characterized in that it is 5400 mm 2 or less.
【0010】さらには、保持材の発泡層表面に形成され
たスキン層が、バフされている前記保持材、または保持
材の表面に被研磨部材が嵌合されるリセス孔を有する角
状或いは円形状のテンプレートが設けられている前記保
持材により課題を解決しうる。Further, the skin layer formed on the surface of the foamed layer of the holding material is a buffed holding material, or an angular or circular shape having a recess hole into which a member to be ground is fitted on the surface of the holding material. The problem can be solved by the holding material provided with a template having a shape.
【0011】ここで、スキン層とは湿式凝固法で作られ
た発泡層の表面に形成された硬い被膜層のことを、テン
プレートとは十分な平面度を有し、耐衝撃性、靱性と耐
摩耗性に優れたエンジニアリングプラスチックで構成さ
れた被加工物が嵌合されるリセス孔を有する枠材の意味
である。その材質には、ガラス入りエポキシ、ベークラ
イト、硬質塩化ビニル等の半剛性材料や更に高硬度な充
填樹脂複合材料等が用いられる。リセス孔とは被研磨部
材を嵌合、脱着するための孔の意味である。Here, the skin layer refers to a hard coating layer formed on the surface of the foam layer formed by the wet solidification method, and the template has sufficient flatness, and has impact resistance, toughness and resistance. It means a frame material having a recess hole into which a workpiece made of an engineering plastic having excellent wear resistance is fitted. As the material, a semi-rigid material such as glass-filled epoxy, bakelite, hard vinyl chloride, or a filled resin composite material having higher hardness is used. The recess hole means a hole for fitting and removing a member to be polished.
【0012】[0012]
【発明の実施の形態】本願発明の保持材を製造するにお
いて湿式発泡層を形成する混合溶液中に含まれる界面活
性剤の量を減らすことあるいは保持材の発泡層を形成す
るがそのものの発泡が弱い界面活性剤を用いること、さ
らには得られた保持材の界面活性剤の量を後工程にて減
ずることにより達成される。本発明に用いられる界面活
性剤としては、例えば、界面活性剤を含む湿式発泡層を
形成する混合溶液を支持体上に塗布して発泡層を生成さ
せ、その後乾燥した時に湿式発泡層の発泡セルの大きさ
が均一で且つ湿式発泡層表面が平滑で且つ湿式発泡層表
面に分散不良もしくは添加剤の表面残留による色ムラが
起こらないような界面活性剤が望ましい。BEST MODE FOR CARRYING OUT THE INVENTION In the production of the holding material of the present invention, the amount of the surfactant contained in the mixed solution for forming the wet foam layer is reduced, or the foam layer of the holding material is formed, but the foaming itself does not occur. This is achieved by using a weak surfactant and further reducing the amount of the surfactant in the obtained holding material in a subsequent step. As the surfactant used in the present invention, for example, a mixed solution for forming a wet foam layer containing a surfactant is applied on a support to form a foam layer, and then dried to form a foam cell of the wet foam layer. It is desirable that the surface active agent has a uniform size, the surface of the wet foam layer is smooth, and the surface of the wet foam layer is not dispersed or uneven color due to residual surface of the additive does not occur.
【0013】界面活性剤の市販品としては、例えばPL
―210(花王株式会社製商品名グリセリンエチレンオ
キシドポリオキシド化合物)があげられる。また、界面
活性剤は通常3部〜10部程度添加されるが、本願発明
においては、0.01部〜2.00部、さらに好ましく
は0.1部〜1.00部の添加量で保持材を製造するも
のである。また、製造後界面活性剤を除去する方法とし
ては、水あるいは、ジメチルホルムアミド、メチルエチ
ルケトン、トルエン、メタノール、エタノール、アセト
ンなどの有機溶媒さらには、それらの混合溶液などの溶
液に溶出する方法がある。Examples of commercially available surfactants include PL
-210 (trade name glycerin ethylene oxide polyoxide compound manufactured by Kao Corporation) can be used. Further, the surfactant is usually added in an amount of about 3 to 10 parts, but in the present invention, the addition amount is 0.01 to 2.00 parts, and more preferably 0.1 to 1.00 parts. The material is manufactured. As a method of removing the surfactant after production, there is a method of eluting it with water, an organic solvent such as dimethylformamide, methyl ethyl ketone, toluene, methanol, ethanol, acetone, or a solution such as a mixed solution thereof.
【0014】本発明で使用される発泡層組成物に添加す
る界面活性剤は、適宜発泡層組成物に配合されるもので
あり、その含有量はウレタン組成物100重量部に対し
て0.01〜2.00重量部が好ましく、さらに好まし
くは0.1〜1.00重量部である。The surfactant to be added to the foam layer composition used in the present invention is appropriately added to the foam layer composition, and its content is 0.01 per 100 parts by weight of the urethane composition. The amount is preferably ˜2.00 parts by weight, more preferably 0.1 to 1.00 parts by weight.
【0015】本発明に使用されるウレタン組成物とは、
一般的に有機ジイソシアネート、ポリオール類及び鎖伸
長剤とからなる。The urethane composition used in the present invention is
It is generally composed of an organic diisocyanate, polyols and a chain extender.
【0016】有機ジイソシアネートとしては、例えばジ
フェニルメタン−4、4‘−ジイソシアネート、キシリ
レンジイソシアネート、ジクロヘキシルメタン−4、4
‘−ジイソシアネート、ヘキサメチレンジイソシアネー
ト等、或いはこれらの混合物が挙げられる。Examples of the organic diisocyanate include diphenylmethane-4,4'-diisocyanate, xylylenediisocyanate, dichlorohexylmethane-4,4.
Examples thereof include'-diisocyanate, hexamethylene diisocyanate and the like, or a mixture thereof.
【0017】またポリオールとしては、ポリエチレンア
ジペートグリコール、ポリプロピレンアジペートグリコ
ール、ポリエチレンプロピレンアジペートグリコール、
ポリブチレンアジペートグリコールポリエチレンブチレ
ンアジペートグリコール、ポリペンタメチレンアジペー
トグリコール等のポリエステルポリオール類、或いはポ
リエチレンエーテルグリコール、ポリプロピレンエーテ
ルグリコール、ポリテトラメチレンエーテルグリコール
等のポリエーテルポリオール類、或いはラクトン環を開
環重合したポリカプロラクトン類の両末端に水酸基を有
する分子量500〜8000のグリコール、或いはポリ
ヘキサメチレンカーボネート、更にはポリヘキサメチレ
ンカーボネートと上述のポリオール類を併合し共重合さ
せたものが挙げられる。As the polyol, polyethylene adipate glycol, polypropylene adipate glycol, polyethylene propylene adipate glycol,
Polybutylene adipate glycol Polyethylene butylene adipate glycol, polyester polyols such as polypentamethylene adipate glycol, polyether polyols such as polyethylene ether glycol, polypropylene ether glycol, and polytetramethylene ether glycol, or polyenes obtained by ring-opening polymerization of lactone ring Examples thereof include glycols having a hydroxyl group at both ends of caprolactone and a molecular weight of 500 to 8000, polyhexamethylene carbonate, and polyhexamethylene carbonate combined with the above-mentioned polyols and copolymerized.
【0018】鎖伸長剤としては、活性水素基を含んだ低
分子化合物、例えばエチレングリコール、プロピレング
リコール、ブチレングリコール、ジエチレングリコール
等のグリコール類、例えばエチレンジアミン、プロピレ
ンジアミン、ブチレンジアミン等のジアミン類、或いは
アミノアルコール等を挙げることができる。As the chain extender, a low molecular weight compound containing an active hydrogen group, for example, glycols such as ethylene glycol, propylene glycol, butylene glycol and diethylene glycol, for example, diamines such as ethylenediamine, propylenediamine and butylenediamine, or amino. Alcohol etc. can be mentioned.
【0019】上述の組成からなるウレタン組成物を溶解
する溶剤としては、例えばジメチルホルムアミド、ジメ
チルスルホキシド、エトラヒドロフラン、ジメチルアセ
トアミド、エチルアセテート、ジオキサン等の水混和性
有機溶剤を挙げることができるが、特にこれらに限定さ
れるものではない。Examples of the solvent for dissolving the urethane composition having the above composition include water-miscible organic solvents such as dimethylformamide, dimethylsulfoxide, etrahydrofuran, dimethylacetamide, ethylacetate and dioxane. It is not particularly limited to these.
【0020】ウレタン組成物の固形分濃度は、好ましく
は10〜40重量%、更に好ましくは15〜30重量%
である。固形分濃度が低すぎると湿式凝固後のウレタン
層表面に大きなうねりが発生し平滑性が悪化する。又固
形分が高すぎる場合空気を巻き込みやすく湿式凝固後の
ウレタン表面に大きな陥没が発生する場合がある。The solid content concentration of the urethane composition is preferably 10 to 40% by weight, more preferably 15 to 30% by weight.
Is. If the solid content concentration is too low, a large amount of waviness occurs on the surface of the urethane layer after wet coagulation and the smoothness deteriorates. Further, if the solid content is too high, air may be easily entrained, and a large depression may occur on the urethane surface after the wet solidification.
【0021】上述の組成に調整されたウレタン組成物
を、すでにコーティングされた熱可塑性樹脂層上にリバ
ースコーター、ナイフコーター等の適宜な塗工手段を用
いてコーティングする。コート量は特に限定しないが1
50g〜1200g/m2が好適である。The urethane composition adjusted to the above composition is coated on the already coated thermoplastic resin layer by using an appropriate coating means such as a reverse coater or a knife coater. The coat amount is not particularly limited, but 1
50g-1200g / m < 2 > is suitable.
【0022】ついで水、DMF(ジメチルホルムアミ
ド)混合溶液中にて湿式凝固せしめた後、脱溶剤のため
の水洗、乾燥をすることにより、コート層に発泡層が得
られる。得られた保持材の表面はそのままでも、十分保
持材として使用可能であり、液晶ガラス等の場合は、こ
の保持材にガラスを水の表面張力により固定し研磨す
る。Then, after wet coagulation in a mixed solution of water and DMF (dimethylformamide), washing with water for solvent removal and drying are performed to obtain a foam layer in the coat layer. The surface of the obtained holding material can be used as a holding material sufficiently even if it is as it is. In the case of liquid crystal glass or the like, glass is fixed to the holding material by surface tension of water and polished.
【0023】また、保持材の表面を、例えばサンドペー
パーを用いて、クリアランス0.3〜0.6mm、ライ
ンスピード1〜10m/分、ペーパー回転数500〜3
000rpmの条件にてバフィングを行う。On the surface of the holding material, for example, sandpaper is used, clearance is 0.3 to 0.6 mm, line speed is 1 to 10 m / min, and paper rotation speed is 500 to 3
Buffing is performed under the condition of 000 rpm.
【0024】シリコンウエハーの場合は、この様に表面
処理された保持材を使用し、ウエハーサイズに開口した
主としてガラスエポキシ樹脂にて形成されているテンプ
レートを配置し、その中に被研磨物であるシリコンウエ
ハーを水吸着して研磨する。In the case of a silicon wafer, the holding material thus surface-treated is used, and a template formed mainly of glass epoxy resin, which is open to the size of the wafer, is arranged, and a template to be polished is placed therein. A silicon wafer is adsorbed with water and polished.
【0025】この時、保持材の表面に被研磨部材が嵌合
されるリセス孔を有する角状或いは円形状のテンプレー
トを設けてもよい。At this time, an angular or circular template having a recess hole into which the member to be polished is fitted may be provided on the surface of the holding material.
【0026】得られた保持材において、それに含有され
る界面活性剤の量は少なければ少ない方が良く、5.0
mg/g保持材以下、さらには3.5mg/g保持材以
下、2.0mg/g保持材以下が好適である。また、実
施例1の条件あるいは研磨中に保持材から発生する泡は
5個/5400mm2以下さらには3個/5400mm2
以下が好適である。In the obtained holding material, the smaller the amount of the surfactant contained in the holding material, the better.
A mg / g holding material or less, more preferably 3.5 mg / g holding material or less, 2.0 mg / g holding material or less is preferable. Further, the number of bubbles generated from the holding material during the conditions of Example 1 or during polishing was 5/5400 mm 2 or less, and further 3/5400 mm 2
The following are preferred:
【0027】[0027]
【実施例】以下、実施例、比較例により本発明を提示す
る。尚、実施例、及び比較例中の「部」は、特に断りの
無い限り重量当たりの比率である「重量部」を意味す
る。EXAMPLES The present invention will be presented below with reference to Examples and Comparative Examples. In addition, "part" in Examples and Comparative Examples means "part by weight" which is a ratio per weight unless otherwise specified.
【0028】泡発生状況評価方法
表面が平滑で且つ剛性の鉄或いはステンレス台の上に6
0mm×90mmの保持材の裏面に両面テープを介在し
て固定する。その保持材の表面に3ccの水を滴下し
て、保持材に水をよくなじませる。80mm×100m
mのガラス板を保持材の上にのせ、2.5gf/cm2
の荷重をかけながら、左右20mmずつ150往復/分
の速度で強制的にガラス板と保持材を擦らせる。Evaluation Method of Bubble Generation Condition 6 is placed on an iron or stainless steel table with a smooth surface and rigidity.
The holding material having a size of 0 mm × 90 mm is fixed to the back surface with a double-sided tape interposed. 3 cc of water is dripped on the surface of the holding material so that the holding material is well blended with the water. 80 mm x 100 m
2.5 gf / cm 2 by placing a glass plate of m on the holding material.
The glass plate and the holding material are forcibly rubbed at a speed of 150 reciprocations / minute for each 20 mm on the right and left while applying the load.
【0029】所定の時間になったら、ガラス板を保持材
からはがして、ガラス板に付着した泡の塊(1個の大き
さが1mm以下で1〜数百個の泡が集まった集合体)の
数と泡の消えるまでの時間を測定する。泡の塊の数に関
しては、ガラス板を保持材から離して30秒以上経って
も残っている泡の数を測定する。泡が消えるまでの時間
に関しては、保持材を離した時を0秒として、泡が完全
になくなるまでの時間とする。At a predetermined time, the glass plate is peeled off from the holding material, and a lump of bubbles attached to the glass plate (an aggregate of 1 to several hundred bubbles with a size of 1 mm or less). And the time until the bubbles disappear. Regarding the number of bubbles, measure the number of bubbles remaining even after 30 seconds or more after separating the glass plate from the holding material. Regarding the time until the bubbles disappear, the time when the holding material is released is 0 second, and the time until the bubbles completely disappear.
【0030】評価の結果の判定は、泡の数が5個以下で
あること、且つ、泡が消えるまでの時間が5分以内であ
るものを○、それ以外のものを×として行った。
[実施例1]まず、支持体と湿式発泡層を接着させるた
めに、ポリエステル−ポリウレタン共重合体をメチルエ
チルケトンで希釈したものをポリエステルシート(東洋
紡株式会社製、クリスパーG1212(厚み0.188
mm))上にナイフコーターでクリアランス0.15m
mにて塗布した。その後、80℃、15分間乾燥し、約
35μmの熱可塑性層を形成しコートしたシートを得
た。ポリテトラメチレンエーテルグリコール(PTM
G)をポリオール成分として用い、ジフェニル−4、4
‘−ジイソシアネート、ジアミンをジメチルホルムアミ
ド中で溶液重合させて、濃度30%のポリウレタンエラ
ストマー溶液を得た。このポリウレタンエラストマー溶
液100部に、カーボンブラック粉3部、ジメチルホル
ムアミド100部、界面活性剤としてPL−210(グ
リセリンエチレンオキシドポリオキシド化合物)1部を
加え、塗布液を得た。得た塗布液を、上記シート上にリ
バースコーターで800g/m2塗布した後、35℃の
凝固浴(水:ジメチルアミド=90:10重量比)中に
て凝固させ、温水で十分脱溶媒した後、150℃にて温
風乾燥を行い、厚み0.8mmの保持材を得た。
[比較例1]塗布液中に添加する界面活性剤が10部で
あること以外は実施例と同一の方法で保持材を製造し
た。
[比較例2]塗布液中に添加する界面活性剤が3部であ
ること以外は実施例と同一の方法で保持材を製造した。
製造した保持材は、泡発生状況評価方法に従い評価し
た。その結果を表1に示した。実施例で明らかな様に、
界面活性剤を減らして作製した高分子弾性発泡体から発
生する泡は、非常に少なく、被研磨部材に付着しても非
常に消滅しやすいものであることがわかる。The evaluation results were evaluated by ◯ when the number of bubbles was 5 or less and the time until the bubbles disappeared within 5 minutes, and by x when the others were not. [Example 1] First, in order to bond a support and a wet foam layer, a polyester sheet obtained by diluting a polyester-polyurethane copolymer with methyl ethyl ketone (manufactured by Toyobo Co., Ltd., Crisper G1212 (thickness 0.188) was used.
mm)) with a knife coater clearance 0.15m
It was applied at m. Then, it was dried at 80 ° C. for 15 minutes to obtain a sheet on which a thermoplastic layer of about 35 μm was formed and coated. Polytetramethylene ether glycol (PTM
G) as a polyol component, diphenyl-4,4
'-Diisocyanate and diamine were solution polymerized in dimethylformamide to obtain a polyurethane elastomer solution having a concentration of 30%. To 100 parts of this polyurethane elastomer solution, 3 parts of carbon black powder, 100 parts of dimethylformamide, and 1 part of PL-210 (glycerin ethylene oxide polyoxide compound) as a surfactant were added to obtain a coating solution. The obtained coating solution was applied on the above sheet by a reverse coater at 800 g / m 2 , coagulated in a coagulation bath at 35 ° C. (water: dimethylamide = 90: 10 weight ratio), and sufficiently desolvated with warm water. Then, hot air drying was performed at 150 ° C. to obtain a holding material having a thickness of 0.8 mm. [Comparative Example 1] A holding material was produced in the same manner as in Example except that the amount of the surfactant added to the coating liquid was 10 parts. [Comparative Example 2] A holding material was produced in the same manner as in Example except that the amount of the surfactant added to the coating liquid was 3 parts.
The produced holding material was evaluated according to the foam generation state evaluation method. The results are shown in Table 1. As is clear from the examples,
It can be seen that bubbles generated from the elastic polymer foam produced by reducing the amount of the surfactant are very small, and even if they are attached to the member to be polished, they are very likely to disappear.
【0031】[0031]
【表1】 [Table 1]
【0032】[0032]
【発明の効果】本発明によれば、本願発明の保持材を研
磨工程に用いることで保持材から発生する泡を抑制で
き、被研磨部材の品質低下を抑制し、且つ製品としての
被研磨部材の歩留まりを向上させることができる。According to the present invention, by using the holding material of the present invention in the polishing step, bubbles generated from the holding material can be suppressed, the deterioration of the quality of the member to be polished can be suppressed, and the member to be polished as a product can be suppressed. The yield can be improved.
【0033】[0033]
Claims (3)
0mg/g保持材以下である被研磨部材の保持材。1. The amount of the surfactant contained in the holding material is 5.
A holding material for a member to be polished having a holding amount of 0 mg / g or less.
400mm2以下であることを特徴とする被研磨部材の
保持材。2. The number of bubbles generated from the holding material during polishing is 5/5.
A holding material for a member to be polished, which is 400 mm 2 or less.
が、バフされている請求項1あるいは2記載の保持材。3. The holding material according to claim 1, wherein the skin layer formed on the surface of the foamed layer of the holding material is buffed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001290689A JP4912548B2 (en) | 2001-09-25 | 2001-09-25 | Method of manufacturing holding member for polished member |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001290689A JP4912548B2 (en) | 2001-09-25 | 2001-09-25 | Method of manufacturing holding member for polished member |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003094323A true JP2003094323A (en) | 2003-04-03 |
| JP4912548B2 JP4912548B2 (en) | 2012-04-11 |
Family
ID=19112959
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001290689A Expired - Lifetime JP4912548B2 (en) | 2001-09-25 | 2001-09-25 | Method of manufacturing holding member for polished member |
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| Country | Link |
|---|---|
| JP (1) | JP4912548B2 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007260855A (en) * | 2006-03-29 | 2007-10-11 | Fujibo Holdings Inc | Polishing cloth for finishing |
| JP2008114364A (en) * | 2007-10-29 | 2008-05-22 | Hoya Corp | Manufacturing method for glass substrate for electronic device, manufacturing method for mask blanks, and manufacturing method for transferring mask |
| JP2009202314A (en) * | 2008-02-29 | 2009-09-10 | Fujibo Holdings Inc | Holding tool |
| JP2010179422A (en) * | 2009-02-06 | 2010-08-19 | Fujibo Holdings Inc | Polishing pad manufacturing method |
| JP2011073111A (en) * | 2009-09-30 | 2011-04-14 | Fujibo Holdings Inc | Polishing pad |
| JP2012110970A (en) * | 2010-11-19 | 2012-06-14 | Fujibo Holdings Inc | Polishing pad and method for manufacturing the same |
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| US4429000A (en) * | 1979-12-11 | 1984-01-31 | Toray Industries, Inc. | Moisture-permeable waterproof coated fabric and method of making the same |
| JPS61266679A (en) * | 1985-05-15 | 1986-11-26 | Kanebo Ltd | Production of leather-like sheet |
| US5024875A (en) * | 1986-09-09 | 1991-06-18 | Burlington Industries, Inc. | Antimicrobial microporous coating |
| JPH0288229A (en) * | 1988-09-26 | 1990-03-28 | Rodeele Nitta Kk | Laminate and support of abrasive member in which the laminate is used and abrasive cloth |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007260855A (en) * | 2006-03-29 | 2007-10-11 | Fujibo Holdings Inc | Polishing cloth for finishing |
| JP2008114364A (en) * | 2007-10-29 | 2008-05-22 | Hoya Corp | Manufacturing method for glass substrate for electronic device, manufacturing method for mask blanks, and manufacturing method for transferring mask |
| JP2009202314A (en) * | 2008-02-29 | 2009-09-10 | Fujibo Holdings Inc | Holding tool |
| JP2010179422A (en) * | 2009-02-06 | 2010-08-19 | Fujibo Holdings Inc | Polishing pad manufacturing method |
| JP2011073111A (en) * | 2009-09-30 | 2011-04-14 | Fujibo Holdings Inc | Polishing pad |
| JP2012110970A (en) * | 2010-11-19 | 2012-06-14 | Fujibo Holdings Inc | Polishing pad and method for manufacturing the same |
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|---|---|
| JP4912548B2 (en) | 2012-04-11 |
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