JP3476367B2 - Resist stripping composition and resist stripping method using the same - Google Patents
Resist stripping composition and resist stripping method using the sameInfo
- Publication number
- JP3476367B2 JP3476367B2 JP21088698A JP21088698A JP3476367B2 JP 3476367 B2 JP3476367 B2 JP 3476367B2 JP 21088698 A JP21088698 A JP 21088698A JP 21088698 A JP21088698 A JP 21088698A JP 3476367 B2 JP3476367 B2 JP 3476367B2
- Authority
- JP
- Japan
- Prior art keywords
- resist
- stripping
- composition
- component
- substrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims description 37
- 238000000034 method Methods 0.000 title claims description 14
- 239000000758 substrate Substances 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 238000005530 etching Methods 0.000 claims description 11
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 10
- 235000000346 sugar Nutrition 0.000 claims description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 5
- 229920001174 Diethylhydroxylamine Polymers 0.000 claims description 4
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 claims description 4
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 claims description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 3
- 239000000243 solution Substances 0.000 description 29
- 238000011282 treatment Methods 0.000 description 11
- 150000005846 sugar alcohols Chemical class 0.000 description 8
- 150000008163 sugars Chemical class 0.000 description 8
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 8
- 206010040844 Skin exfoliation Diseases 0.000 description 7
- 238000003860 storage Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- -1 glycol monoalkyl ethers Chemical class 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- 239000004973 liquid crystal related substance Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920002120 photoresistant polymer Polymers 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 229910001069 Ti alloy Inorganic materials 0.000 description 2
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 150000002443 hydroxylamines Chemical class 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 230000003405 preventing effect Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229960002920 sorbitol Drugs 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 238000001039 wet etching Methods 0.000 description 2
- 239000000811 xylitol Substances 0.000 description 2
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 2
- 235000010447 xylitol Nutrition 0.000 description 2
- 229960002675 xylitol Drugs 0.000 description 2
- XGIKILRODBEJIL-UHFFFAOYSA-N 1-(ethylamino)ethanol Chemical compound CCNC(C)O XGIKILRODBEJIL-UHFFFAOYSA-N 0.000 description 1
- PYVRVRFVLRNJLY-KTKRTIGZSA-N 1-oleoyl phosphatidylethanolamine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)COP(O)(=O)OCCN PYVRVRFVLRNJLY-KTKRTIGZSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical group NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical group COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- YVNRSOMGUGTRMU-UHFFFAOYSA-N 6-ethyl-5-methylphenanthridin-5-ium-3,8-diamine;bromide Chemical compound [Br-].C1=C(N)C=C2C(CC)=[N+](C)C3=CC(N)=CC=C3C2=C1 YVNRSOMGUGTRMU-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 235000018087 Spondias lutea Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000005262 alkoxyamine group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical group O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- MAKDTFFYCIMFQP-UHFFFAOYSA-N titanium tungsten Chemical compound [Ti].[W] MAKDTFFYCIMFQP-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Photosensitive Polymer And Photoresist Processing (AREA)
- Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明はレジスト用剥離液組
成物およびこれを用いたレジスト剥離方法に関する。さ
らに詳しくは、ICやLSI等の半導体素子あるいは液
晶パネル素子の製造に好適に使用される、レジスト膜の
剥離性に優れ、高温下での保存安定性に優れたレジスト
用剥離液組成物およびこれを用いたレジスト剥離方法に
関する。TECHNICAL FIELD The present invention relates to a resist stripping composition and a resist stripping method using the same. More specifically, a resist stripping composition for use in the production of semiconductor devices such as ICs and LSIs or liquid crystal panel devices, which has excellent releasability of a resist film and excellent storage stability at high temperatures, and the same. The present invention relates to a resist stripping method using.
【0002】[0002]
【従来の技術】ICやLSI等の半導体素子や液晶パネ
ル素子は、基板上に蒸着等により形成されたネサ膜等の
導電性金属膜やSiO2膜等の絶縁膜上にホトレジスト
を均一に塗布し、これを選択的に露光、現像処理をして
レジストパターンを形成し、このパターンをマスクとし
て上記導電性金属膜や絶縁膜を選択的にエッチングし、
微細回路を形成した後、不要のレジスト層を剥離液で除
去して製造される。2. Description of the Related Art For semiconductor elements such as ICs and LSIs and liquid crystal panel elements, a photoresist is uniformly applied to a conductive metal film such as a NES film formed on a substrate by vapor deposition or an insulating film such as a SiO 2 film. Then, this is selectively exposed and developed to form a resist pattern, and the conductive metal film or insulating film is selectively etched using this pattern as a mask,
After forming a fine circuit, an unnecessary resist layer is removed with a stripping solution to manufacture.
【0003】このレジスト層を除去する剥離液として、
従来、アルキルベンゼンスルホン酸を必須成分とした有
機スルホン酸系剥離液やモノエタノールアミン等の有機
アミンを必須成分とした有機アミン系剥離液が使用され
てきた。前者の有機スルホン酸系剥離液は、毒性の高い
フェノール化合物やクロロベンゼン等の有機溶剤が併用
されることから作業性が悪く、また環境問題が発生する
上に、基板の導電性金属膜等が腐食されやすいという欠
点を有している。これに対して、後者の有機アミン系剥
離液は有機スルホン酸系剥離液に比べて毒性が低く、廃
液処理に煩雑な処理が必要でなく、またAlやCu等を
含む基板の腐食防止効果に優れることなどから今日広く
使用されている。As a stripping solution for removing this resist layer,
Conventionally, an organic sulfonic acid-based stripping solution containing an alkylbenzene sulfonic acid as an essential component and an organic amine-based stripping solution containing an organic amine such as monoethanolamine as an essential component have been used. The former organic sulfonic acid-based stripping solution has poor workability because it is used in combination with highly toxic organic compounds such as phenolic compounds and chlorobenzene, and also causes environmental problems and corrodes the conductive metal film of the substrate. It has the drawback that it is easy to get rid of. On the other hand, the latter organic amine-based stripping solution is less toxic than the organic sulfonic acid-based stripping solution, does not require complicated treatment for waste liquid treatment, and has the effect of preventing corrosion of substrates containing Al, Cu, etc. It is widely used today because of its superiority.
【0004】有機アミン系剥離液処理は、処理温度が比
較的高温で、例えば、剥離液槽中の剥離液を60〜80
℃程度に加熱し、この加温された剥離液に基板を浸漬し
て剥離処理を行う浸漬法や、上記温度に加温された剥離
液を基板上に吹き付けるシャワー法等が用いられてい
る。このような剥離処理においては、剥離液を60〜8
0℃の高温状態に長時間保持しても、その特性(剥離
性、防食性)が損なわれるものであってはならない。特
に液晶パネル素子等に利用される大型ガラス基板は、大
きくとも直径300mmといわれる半導体集積回路用基
板に比べて、例えば360mm×460mm、550m
m×650mm、600mm×720mmなど、かなり
大型のものが用いられる。それゆえ剥離液槽も基板の大
きさに比例して大型になるため、剥離液が蒸発しやす
く、その組成が変化しやすくなる。In the organic amine-based stripping solution treatment, the stripping solution in the stripping solution tank is treated at a relatively high temperature of 60 to 80, for example.
A dipping method in which the substrate is heated to about 0 ° C. and immersed in the heated stripping solution to perform stripping, a shower method in which the stripping solution heated to the above temperature is sprayed onto the substrate, and the like are used. In such a stripping treatment, a stripping solution of 60 to 8 is used.
Even if it is kept at a high temperature of 0 ° C. for a long time, its characteristics (peelability, corrosion resistance) should not be impaired. In particular, a large glass substrate used for a liquid crystal panel element or the like has a size of, for example, 360 mm × 460 mm, 550 m, as compared with a substrate for a semiconductor integrated circuit which is said to have a diameter of 300 mm at the maximum.
A considerably large size such as m × 650 mm, 600 mm × 720 mm is used. Therefore, the stripping solution tank also becomes large in proportion to the size of the substrate, so that the stripping solution easily evaporates and its composition easily changes.
【0005】従来、レジスト用剥離液組成物としては、
例えば、アルカノールアミン類、アルコキシアルキルア
ミン類またはアルコキシアルカノールアミン類、グリコ
ールモノアルキルエーテル、糖または糖アルコール類、
および水からなるレジスト剥離剤組成物(特開平8−1
90205号公報)、アルカノールアミン類、アルコキ
シアルキルアミン類またはアルコキシアルカノールアミ
ン類、酸アミド類、糖または糖アルコール類、および水
からなるレジスト剥離剤組成物(特開平8−20205
1号公報)、アルカノールアミン類、アルコキシアルキ
ルアミン類またはアルコキシアルカノールアミン類、グ
リコールモノアルキルエーテル、糖または糖アルコール
類、第四級アンモニウム水酸化物、および水からなるレ
ジスト剥離剤組成物(特開平8−262746号公
報)、アルカノールアミン類、アルコキシアミン類また
はアルコキシアルカノールアミン類、ヒドロキシルアミ
ン類、糖または糖アルコール類、界面活性剤、および水
からなるレジスト剥離剤組成物(特開平9−54442
号公報)、アルカノールアミン類、ジエチレングリコー
ルモノアルキルエーテル、糖または糖アルコール類、
N,N−ジエチルヒドロキシルアミン、および水からな
るレジスト用剥離液組成物(特開平9−152721号
公報)、pKaが7.5〜13のアミン類、ヒドロキシ
ルアミン類、水溶性有機溶媒、防食剤、および水からな
るレジスト用剥離液組成物(特開平9−96911号公
報)等が挙げられる。Conventionally, as a stripping composition for resist,
For example, alkanolamines, alkoxyalkylamines or alkoxyalkanolamines, glycol monoalkyl ethers, sugars or sugar alcohols,
And a resist stripper composition comprising water (Japanese Patent Laid-Open No. 8-1
90205), alkanolamines, alkoxyalkylamines or alkoxyalkanolamines, acid amides, sugars or sugar alcohols, and water (JP-A-8-20205).
No. 1), alkanolamines, alkoxyalkylamines or alkoxyalkanolamines, glycol monoalkyl ethers, sugars or sugar alcohols, quaternary ammonium hydroxides, and water. No. 8-262746), alkanolamines, alkoxyamines or alkoxyalkanolamines, hydroxylamines, sugars or sugar alcohols, surfactants, and water (JP-A-9-54442).
Gazette), alkanolamines, diethylene glycol monoalkyl ethers, sugars or sugar alcohols,
Stripping solution composition for resist consisting of N, N-diethylhydroxylamine and water (JP-A-9-152721), amines having pKa of 7.5 to 13, hydroxylamines, water-soluble organic solvent, anticorrosive agent And a resist stripping composition for resist (Japanese Patent Laid-Open No. 9-96911).
【0006】上記各公報に記載の組成物は、おもにアッ
シング処理後に生じたホトレジスト変質膜や金属デポジ
ションの剥離を目的としたものである。The compositions described in the above-mentioned respective publications are mainly intended for peeling off a photoresist-altered film or a metal deposition film formed after an ashing process.
【0007】上記各公報記載の組成物のうち、特開平8
−190205号公報、特開平8−202051号公
報、特開平8−262746号公報、特開平9−969
11号公報に記載の組成物は、レジスト変質膜に対して
はほぼ満足できる剥離性を示すものの、変質していない
レジスト膜に対する剥離性については必ずしも十分に満
足し得る程度の効果を奏するまでには至っていない。Among the compositions described in each of the above publications, JP-A-8
-190205, JP-A-8-202051, JP-A-8-262746, JP-A-9-969.
Although the composition described in JP-A No. 11 shows almost satisfactory releasability with respect to a resist-altered film, it does not necessarily exhibit sufficient releasability with respect to an unaltered resist film. Has not arrived.
【0008】特開平9−54442号公報、特開平9−
152721号公報に記載の組成物では、水分が多くな
りすぎると基板を腐食する可能性が高くなる一方、水分
が少なすぎると引火点が低くなり作業上の危険が大きく
なるおそれがある。さらに、水が糖または糖アルコール
類を溶解させる唯一の成分でもあるため、水分が少ない
場合、あるいは適度な水分含有量であっても、高温の状
態で長時間使用する場合に、剥離液組成物中の糖または
糖アルコール類の層と他の成分の層との間で層の分離が
起こり得る。Japanese Unexamined Patent Publication No. 9-54442 and Japanese Unexamined Patent Publication No. 9-
In the composition disclosed in Japanese Patent No. 152721, when the water content is too high, the substrate is likely to be corroded, while when the water content is too low, the flash point is lowered and the work risk may be increased. Furthermore, since water is also the only component that dissolves sugars or sugar alcohols, the stripping solution composition is used when the water content is low or when the water content is moderate and the material is used at a high temperature for a long time. Layer separation can occur between the sugar or sugar alcohol layers and the other ingredient layers therein.
【0009】[0009]
【発明が解決しようとする課題】本発明は、特に、変質
していないレジスト層の剥離性に特に優れるとともに、
高温下での保存安定性に優れるレジスト用剥離液組成物
およびこれを用いたレジスト剥離方法を提供することを
目的とする。The present invention is particularly excellent in the releasability of a resist layer that has not deteriorated, and
An object of the present invention is to provide a resist stripping composition having excellent storage stability at high temperatures and a resist stripping method using the same.
【0010】[0010]
【課題を解決するための手段】 すなわち本発明は、
(a)アルカノールアミン類、(b)N,N−ジエチル
ヒドロキシルアミン、(c)糖類、(d)N−メチル−
2−ピロリドン、ジメチルスルホキシドの中から選ばれ
るいずれか1種以上、および(e)水を含有してなるレ
ジスト用剥離液組成物に関する。Means for Solving the Problems That is, the present invention is
(A) Alkanolamines, (b) N, N-diethylhydroxylamine, (c) saccharides, (d) N-methyl-
2-pyrrolidone, any one or more selected from among di-methyl sulfoxide, and (e) a resist stripping solution composition comprising water.
【0011】また本発明は、(I)基板上にレジスト層
を設ける工程、(II)該レジスト層を選択的に露光す
る工程、(III)露光後のレジスト層を現像してレジ
ストパターンを設ける工程、(IV)該レジストパター
ンをマスクとして該基板をエッチングする工程、および
(V)エッチング後のレジストパターンを基板より剥離
する工程からなるレジスト剥離方法において、上記レジ
スト用剥離液組成物を用いて、エッチング後のレジスト
パターンを剥離することを特徴とするレジスト剥離方法
に関する。In the present invention, (I) a step of forming a resist layer on a substrate, (II) a step of selectively exposing the resist layer, and (III) developing the exposed resist layer to form a resist pattern. In the resist stripping method comprising the steps of: (IV) etching the substrate using the resist pattern as a mask; and (V) stripping the etched resist pattern from the substrate, the resist stripping composition is used. The present invention relates to a resist stripping method, which strips a resist pattern after etching.
【0012】[0012]
【発明の実施の形態】以下に、本発明のレジスト用剥離
液組成物について詳述する。BEST MODE FOR CARRYING OUT THE INVENTION The stripping solution composition for resist of the present invention is described in detail below.
【0013】(a)成分のアルカノールアミン類として
は、具体的には、例えばモノエタノールアミン、ジエタ
ノールアミン、トリエタノールアミン、エチルアミノエ
タノール、ジメチルアミノエタノール、ジエチルアミノ
エタノール、2−(2−アミノエトキシ)エタノール等
が挙げられ、中でもモノエタノールアミン、ジエタノー
ルアミン、2−2(アミノエトキシ)エタノールが好適
に用いられる。これらは単独で用いてもよく、あるいは
2種以上を組み合わせて用いてもよい。Specific examples of the alkanolamines as the component (a) include monoethanolamine, diethanolamine, triethanolamine, ethylaminoethanol, dimethylaminoethanol, diethylaminoethanol and 2- (2-aminoethoxy) ethanol. Etc. Among them, monoethanolamine, diethanolamine, and 2-2 (aminoethoxy) ethanol are preferably used. These may be used alone or in combination of two or more.
【0014】本発明剥離液組成物中、(a)成分の配合
量の上限は40重量%が好ましく、特には30重量%が
好ましい。また下限は5重量%が好ましく、特には10
重量%が好ましい。In the stripper composition of the present invention, the upper limit of the amount of the component (a) to be blended is preferably 40% by weight, and particularly preferably 30% by weight. The lower limit is preferably 5% by weight, particularly 10
Weight percent is preferred.
【0015】(b)成分としてのN,N−ジエチルヒド
ロキシルアミンは、N(C2H5)2OHで表される化合
物である。N, N-diethylhydroxylamine as the component (b) is a compound represented by N (C 2 H 5 ) 2 OH.
【0016】本発明剥離液組成物中、(b)成分の配合
量の上限は30重量%が好ましく、特には20重量%が
好ましい。また下限は5重量%が好ましく、特には10
重量%が好ましい。In the stripper composition of the present invention, the upper limit of the amount of the component (b) compounded is preferably 30% by weight, particularly preferably 20% by weight. The lower limit is preferably 5% by weight, particularly 10
Weight percent is preferred.
【0017】(c)成分の糖類としては、一般にC
n(H2O)mで表されるいわゆる糖や、これら糖のカル
ボニル基を還元して得られる糖アルコール等が用いら
れ、具体的にはD−ソルビトール、アラビトール、マン
ニトール、キシリトール、ショ糖、でんぷん等が挙げら
れ、中でもキシリトール、D−ソルビトールが好まし
い。これらは単独で用いてもよく、あるいは2種以上を
組み合わせて用いてもよい。As the saccharide as the component (c), C is generally
So-called sugars represented by n (H 2 O) m , sugar alcohols obtained by reducing the carbonyl groups of these sugars, and the like are used, and specifically, D-sorbitol, arabitol, mannitol, xylitol, sucrose, Examples of the starch include xylitol and D-sorbitol. These may be used alone or in combination of two or more.
【0018】本発明剥離液組成物中、(c)成分の配合
量の上限は30重量%が好ましく、特には25重量%が
好ましい。また下限は2重量%が好ましく、特には5重
量%が好ましい。In the stripper composition of the present invention, the upper limit of the amount of component (c) to be blended is preferably 30% by weight, and particularly preferably 25% by weight. The lower limit is preferably 2% by weight, particularly 5% by weight.
【0019】 (d)成分としては、N−メチル−2−
ピロリドン、ジメチルスルホキシド、またはこれらの混
合溶媒が用いられる。As the component (d), N-methyl-2-
Pyrrolidone, di-methyl sulfoxide, or a mixed solvent thereof, are used.
【0020】本発明剥離液組成物中、(d)成分の配合
量の上限は40重量%が好ましく、特には30重量%が
好ましい。また下限は5重量%が好ましく、特には10
重量%が好ましい。In the stripper composition of the present invention, the upper limit of the amount of the component (d) to be blended is preferably 40% by weight, particularly 30% by weight. The lower limit is preferably 5% by weight, particularly 10
Weight percent is preferred.
【0021】(e)成分としての水は、(a)成分等に
必然的に含まれているものであるが、さらに加えてその
配合量を調整してもよい。(e)成分の配合割合は、本
発明剥離液組成物中、上記(a)〜(d)成分の配合量
の残部である。Water as the component (e) is inevitably contained in the component (a) and the like, but the amount thereof may be adjusted in addition. The blending ratio of the component (e) is the balance of the blending amounts of the components (a) to (d) in the stripper composition of the present invention.
【0022】本発明では、(a)〜(e)成分を上述し
た配合割合範囲とすることにより、剥離性、高温での保
存特性、防食性により一層優れた効果を奏することがで
きる。In the present invention, by making the components (a) to (e) within the above-mentioned blending ratio range, more excellent effects can be achieved in terms of releasability, storage characteristics at high temperatures, and anticorrosion properties.
【0023】本発明のレジスト用剥離液組成物は、ネガ
型およびポジ型レジストを含めてアルカリ水溶液で現像
可能なレジストに有利に使用できる。このようなレジス
トとしては、(i)ナフトキノンジアジド化合物とノボ
ラック樹脂を含有するポジ型レジスト、(ii)露光に
より酸を発生する化合物、酸により分解しアルカリ水溶
液に対する溶解性が増大する化合物およびアルカリ可溶
性樹脂を含有するポジ型レジスト、(iii)露光によ
り酸を発生する化合物、酸により分解しアルカリ水溶液
に対する溶解性が増大する基を有するアルカリ可溶性樹
脂を含有するポジ型レジスト、および(iv)光により
酸を発生する化合物、架橋剤およびアルカリ可溶性樹脂
を含有するネガ型レジスト等が挙げられるが、これらに
限定されるものではない。The resist stripping composition of the present invention can be advantageously used for resists that can be developed with an aqueous alkaline solution, including negative and positive resists. Examples of such a resist include (i) a positive resist containing a naphthoquinonediazide compound and a novolak resin, (ii) a compound that generates an acid upon exposure to light, a compound that decomposes with an acid to increase its solubility in an alkaline aqueous solution, and an alkali-soluble compound. A positive resist containing a resin, (iii) a compound that generates an acid upon exposure to light, a positive resist containing an alkali-soluble resin having a group that decomposes by an acid to increase solubility in an aqueous alkaline solution, and (iv) by light Examples thereof include, but are not limited to, a negative resist containing a compound that generates an acid, a crosslinking agent, and an alkali-soluble resin.
【0024】本発明のレジスト剥離方法は、(I)基板
上にレジスト層を設ける工程、(II)該レジスト層を
選択的に露光する工程、(III)露光後のレジスト層
を現像してレジストパターンを設ける工程、(IV)該
レジストパターンをマスクとして該基板をエッチングす
る工程、および(V)エッチング後のレジストパターン
を基板より剥離する工程からなるレジスト剥離方法にお
いて、上記レジスト用剥離液組成物を用いて、エッチン
グ後のレジストパターンを剥離することからなる。The resist stripping method of the present invention comprises (I) a step of providing a resist layer on a substrate, (II) a step of selectively exposing the resist layer, and (III) developing the resist layer after exposure to form a resist. A resist stripping composition comprising the steps of: providing a pattern; (IV) etching the substrate using the resist pattern as a mask; and (V) stripping the etched resist pattern from the substrate. Is used to peel off the resist pattern after etching.
【0025】基板としては、例えば金属層を形成した基
板等が挙げられる。金属層としては、アルミニウム(A
l);アルミニウム−ケイ素(Al−Si)、アルミニ
ウム−ケイ素−銅(Al−Si−Cu)等のアルミニウ
ム合金(Al合金);純チタン(Ti);チタンナイト
ライド(TiN)、チタンタングステン(TiW)等の
チタン合金(Ti合金)等が挙げられるが、これらに限
定されるものでない。Examples of the substrate include a substrate having a metal layer formed thereon. As the metal layer, aluminum (A
l); Aluminum alloys (Al alloys) such as aluminum-silicon (Al-Si) and aluminum-silicon-copper (Al-Si-Cu); pure titanium (Ti); titanium nitride (TiN), titanium tungsten (TiW). ) And other titanium alloys (Ti alloys) and the like, but are not limited to these.
【0026】塗布、乾燥、露光、現像、およびエッチン
グ処理は、いずれも慣用的な手段であり、特に限定され
ない。エッチングはウェットエッチング、ドライエッチ
ングのいずれも用いられ得るが、本発明剥離液組成物
は、ウェットエッチング後のレジスト膜の剥離に特に好
適に用いられ得る。特に液晶パネル素子等に用いられる
ガラス基板等においては、エッチング液(エッチャン
ト)としては、リン酸、硝酸、酢酸等の酸性エッチング
液が好まく用いられる。The coating, drying, exposing, developing and etching treatments are all conventional means and are not particularly limited. Either wet etching or dry etching can be used as the etching, but the stripping composition of the present invention can be particularly preferably used for stripping the resist film after the wet etching. Particularly in a glass substrate or the like used for a liquid crystal panel element or the like, an acidic etching liquid such as phosphoric acid, nitric acid or acetic acid is preferably used as an etching liquid (etchant).
【0027】なお、上記(III)の現像工程、(V)
の剥離工程の後、慣用的に施されている純水や低級アル
コール等を用いたリンス処理および乾燥処理を施しても
よい。The developing step (III), (V)
After the stripping step, a rinsing treatment and a drying treatment using pure water, lower alcohol, or the like, which are conventionally performed, may be performed.
【0028】剥離処理は通常、浸漬法、シャワー法によ
り施される。剥離時間は、剥離される十分な時間であれ
ばよく、特に限定されるものではない。なお、その際の
剥離液の温度は、本発明の剥離液組成物を用いた剥離方
法においては、60〜80℃の高温でも金属膜に対する
腐食防止効果が高く、また特に変質されていないレジス
ト膜の剥離性に優れる。本発明剥離液組成物は、60〜
80℃の高温下でも保存安定性に優れ、組成変化がな
く、循環使用が可能であることから、製造コストの低減
化を図ることができる等の効果を奏する。The peeling treatment is usually performed by a dipping method or a shower method. The peeling time is not particularly limited as long as it is a sufficient peeling time. In addition, the temperature of the stripping solution at that time is high in the corrosion preventing effect on the metal film even at a high temperature of 60 to 80 ° C. in the stripping method using the stripping solution composition of the present invention, and the resist film not particularly denatured It has excellent releasability. The stripper composition of the present invention has a viscosity of 60 to
It has excellent storage stability even at a high temperature of 80 ° C., does not change in composition, and can be reused. Therefore, it has effects such as reduction of manufacturing cost.
【0029】[0029]
【実施例】次に、実施例により本発明をさらに詳細に説
明するが、本発明はこれらの例によってなんら限定され
るものではない。The present invention will be described in more detail by way of examples, which should not be construed as limiting the invention thereto.
【0030】(実施例1〜5、比較例1〜7)シリコン
ウェーハ上にAl配線が形成された基板上に、ナフトキ
ノンジアジド化合物とノボラック樹脂からなるポジ型ホ
トレジストであるTHMR−iP3300(東京応化工
業(株)製)をスピンナーで塗布し、90℃にて90秒
間のプリベークを施し、膜厚2.0μmのレジスト層を
形成した。このレジスト層をNSR−2005i10D
(ニコン(株)製)を用いてマスクパターンを介して露
光し、2.38重量%テトラメチルアンモニウムヒドロ
キシド(TMAH)水溶液にて現像し、レジストパター
ンを形成した。次いで120℃で90秒間のポストベー
クを行った。(Examples 1 to 5 and Comparative Examples 1 to 7) THMR-iP3300 (Tokyo Ohka Kogyo Co., Ltd.), which is a positive photoresist composed of a naphthoquinonediazide compound and a novolac resin, is formed on a substrate having Al wiring formed on a silicon wafer. Co., Ltd.) was applied with a spinner and prebaked at 90 ° C. for 90 seconds to form a resist layer having a film thickness of 2.0 μm. This resist layer is NSR-2005i10D
(Nikon Corp.) was used for exposure through a mask pattern, followed by development with a 2.38 wt% tetramethylammonium hydroxide (TMAH) aqueous solution to form a resist pattern. Then, post baking was performed at 120 ° C. for 90 seconds.
【0031】[レジスト膜の剥離性試験]次に、上記の
条件で形成したレジストパターンを有するシリコンウェ
ーハを、リン酸、硝酸、酢酸の混酸系のエッチャントに
よりウェットエッチング処理し、その後、純水で洗浄し
た。[Resistant film releasability test] Next, the silicon wafer having a resist pattern formed under the above conditions is wet-etched with a mixed acid type etchant of phosphoric acid, nitric acid, and acetic acid, and then with pure water. Washed.
【0032】上記処理済み基板に対し、表1に示す各組
成の剥離液組成物(60℃に保持)をシャワー法により
吹き付けることにより、それぞれレジスト膜剥離処理を
行った。剥離処理後の基板を純水で十分にリンス処理
し、このときのレジスト膜の剥離性をSEM(走査型電
子顕微鏡)写真の観察により評価した。結果を表2に示
す。A resist film peeling treatment was carried out by spraying a stripping solution composition of each composition shown in Table 1 (held at 60 ° C.) onto the treated substrate by a shower method. The substrate after the peeling treatment was sufficiently rinsed with pure water, and the peelability of the resist film at this time was evaluated by observing SEM (scanning electron microscope) photographs. The results are shown in Table 2.
【0033】なお、レジスト膜の剥離性は、以下のよう
に評価した。The releasability of the resist film was evaluated as follows.
【0034】A: レジスト膜の剥離が完全になされて
いる
B: レジスト膜の残渣物が残っているA: The resist film is completely peeled off B: The residue of the resist film remains
【0035】[加熱下の保存安定性]さらに加熱下での
保存安定性を評価するために、表1に示す組成の剥離液
を60℃に加熱し、その温度を維持した。このときの溶
液の状態を観察し評価した。結果を表2に示す。[Storage Stability Under Heating] Further, in order to evaluate the storage stability under heating, the stripping solution having the composition shown in Table 1 was heated to 60 ° C. and maintained at that temperature. The state of the solution at this time was observed and evaluated. The results are shown in Table 2.
【0036】なお、剥離液の状態は以下のように評価し
た。The state of the stripping solution was evaluated as follows.
【0037】A: 48時間以上経過しても溶液に変化
がみられなかった
B: 12時間経過した時点で溶液が二層に分離したA: No change was observed in the solution after 48 hours or more. B: The solution separated into two layers after 12 hours.
【0038】[0038]
【表1】 [Table 1]
【0039】 なお、表1中、MEAはモノエタノール
アミンを;AEEは2−(2−アミノエトキシ)エタノ
ールを;TETはトリエチレンテトラミンを;NMPは
N−メチル−2−ピロリドンを;DMSOはジメチルス
ルホキシドを;DEMBはジエチレングリコールモノブ
チルエーテルを;DEMMはジエチレングリコールモノ
メチルエーテルを;TMAHはテトラメチルアンモニウ
ムヒドロキシドを;HAはヒドロキシルアミンを;PG
MOPEはプロピレングリコールモノ−P−オクチルフ
ェニルエーテルを、それぞれ示す。In Table 1, MEA is monoethanolamine; AEE is 2- (2-aminoethoxy) ethanol; TET is triethylenetetramine; NMP is N-methyl-2-pyrrolidone; DMSO is diethylenediamine. DEMB is diethylene glycol monobutyl ether; DEMM is diethylene glycol monomethyl ether; TMAH is tetramethylammonium hydroxide; HA is hydroxylamine; PG
MOPE represents propylene glycol mono-P-octyl phenyl ether, respectively.
【0040】[0040]
【表2】 [Table 2]
【0041】[0041]
【発明の効果】以上詳述したように本発明によれば、レ
ジスト層の剥離性に優れ、高温下での保存安定性に優れ
るレジスト用剥離液組成物およびこれを用いたレジスト
剥離方法が提供される。本発明は特に、液晶パネル素子
の製造等に用いられる大型の基板上に形成されたレジス
ト層の剥離に好適に使用される。本発明により、高温で
の剥離処理においても剥離液の組成変化がなく、剥離液
の循環使用が可能となり、製造コストの低減化を図るこ
とができる等の効果が得られる。As described above in detail, according to the present invention, there is provided a resist stripping composition which is excellent in stripping property of a resist layer and storage stability at high temperature, and a resist stripping method using the same. To be done. The present invention is particularly preferably used for peeling a resist layer formed on a large-sized substrate used for manufacturing a liquid crystal panel element or the like. According to the present invention, the composition of the stripping solution does not change even in stripping treatment at high temperature, the stripping solution can be circulated and used, and the manufacturing cost can be reduced.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平9−54442(JP,A) 特開 平9−152721(JP,A) 特開 平7−271057(JP,A) 特開 平8−202051(JP,A) (58)調査した分野(Int.Cl.7,DB名) G03F 7/00 - 7/42 H01L 21/027 ─────────────────────────────────────────────────── ─── Continuation of the front page (56) Reference JP-A-9-54442 (JP, A) JP-A-9-152721 (JP, A) JP-A-7-271057 (JP, A) JP-A-8- 202051 (JP, A) (58) Fields surveyed (Int.Cl. 7 , DB name) G03F 7/ 00-7/42 H01L 21/027
Claims (4)
N,N−ジエチルヒドロキシルアミン、(c)糖類、
(d)N−メチル−2−ピロリドン、ジメチルスルホキ
シドの中から選ばれるいずれか1種以上、および(e)
水を含有してなる、レジスト用剥離液組成物。1. (a) Alkanolamines, (b)
N, N-diethylhydroxylamine, (c) sugar,
(D) N-methyl-2-pyrrolidone, any one or more selected from among di-methyl sulfoxide, and (e)
A resist stripping composition comprising water.
エタノールアミン、2−(2−アミノエトキシ)エタノ
ールの中から選ばれるいずれか1種以上である、請求項
1記載のレジスト用剥離液組成物。2. The resist stripping composition according to claim 1, wherein the component (a) is at least one selected from monoethanolamine, diethanolamine and 2- (2-aminoethoxy) ethanol.
分が5〜30重量%、(c)成分が2〜30重量%、
(d)成分が5〜40重量%配合され、残部が(e)成
分である、請求項1または2記載のレジスト用剥離液組
成物。3. The component (a) is 5 to 40% by weight, the component (b) is 5 to 30% by weight, the component (c) is 2 to 30% by weight,
The resist stripper composition according to claim 1 or 2, wherein the component (d) is blended in an amount of 5 to 40% by weight, and the balance is the component (e).
程、(II)該レジスト層を選択的に露光する工程、
(III)露光後のレジスト層を現像してレジストパタ
ーンを設ける工程、(IV)該レジストパターンをマス
クとして該基板をエッチングする工程、および(V)エ
ッチング後のレジストパターンを基板より剥離する工程
からなるレジスト剥離方法において、請求項1〜3のい
ずれかに記載のレジスト用剥離液組成物を用いて、エッ
チング後のレジストパターンを剥離することを特徴とす
る、レジスト剥離方法。4. (I) providing a resist layer on the substrate, (II) selectively exposing the resist layer,
From (III) a step of developing a resist layer after exposure to provide a resist pattern, (IV) a step of etching the substrate using the resist pattern as a mask, and (V) a step of peeling the resist pattern after etching from the substrate In the resist stripping method, the resist stripping composition according to any one of claims 1 to 3 is used to strip the resist pattern after etching.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21088698A JP3476367B2 (en) | 1998-07-27 | 1998-07-27 | Resist stripping composition and resist stripping method using the same |
TW88111591A TW594425B (en) | 1998-07-27 | 1999-07-08 | Photoresist stripping liquid compositions and a method of stripping photoresists using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21088698A JP3476367B2 (en) | 1998-07-27 | 1998-07-27 | Resist stripping composition and resist stripping method using the same |
Publications (2)
Publication Number | Publication Date |
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JP2000047400A JP2000047400A (en) | 2000-02-18 |
JP3476367B2 true JP3476367B2 (en) | 2003-12-10 |
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Application Number | Title | Priority Date | Filing Date |
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JP21088698A Expired - Fee Related JP3476367B2 (en) | 1998-07-27 | 1998-07-27 | Resist stripping composition and resist stripping method using the same |
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JP (1) | JP3476367B2 (en) |
TW (1) | TW594425B (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
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KR100434491B1 (en) * | 2001-08-17 | 2004-06-05 | 삼성전자주식회사 | Resist or etching by-products removing composition and resist removing method using the same |
KR100438015B1 (en) * | 2001-10-10 | 2004-06-30 | 엘지.필립스 엘시디 주식회사 | Cu-compatible Resist removing composition |
JP4314320B2 (en) | 2002-04-10 | 2009-08-12 | 三菱電機株式会社 | Method for manufacturing compound semiconductor device |
JP2005173369A (en) | 2003-12-12 | 2005-06-30 | Tokyo Ohka Kogyo Co Ltd | Method for removing resist pattern |
JP5659729B2 (en) * | 2010-11-24 | 2015-01-28 | 三菱瓦斯化学株式会社 | Photoresist stripper composition |
-
1998
- 1998-07-27 JP JP21088698A patent/JP3476367B2/en not_active Expired - Fee Related
-
1999
- 1999-07-08 TW TW88111591A patent/TW594425B/en not_active IP Right Cessation
Also Published As
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TW594425B (en) | 2004-06-21 |
JP2000047400A (en) | 2000-02-18 |
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