TW267186B - - Google Patents
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- TW267186B TW267186B TW083109330A TW83109330A TW267186B TW 267186 B TW267186 B TW 267186B TW 083109330 A TW083109330 A TW 083109330A TW 83109330 A TW83109330 A TW 83109330A TW 267186 B TW267186 B TW 267186B
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- stripping
- acid
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- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 67
- 239000000463 material Substances 0.000 claims description 37
- 239000003795 chemical substances by application Substances 0.000 claims description 27
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 24
- 239000010931 gold Substances 0.000 claims description 23
- 229910052737 gold Inorganic materials 0.000 claims description 23
- -1 unsaturated _ Chemical compound 0.000 claims description 23
- 238000005260 corrosion Methods 0.000 claims description 20
- 230000007797 corrosion Effects 0.000 claims description 20
- 229920002120 photoresistant polymer Polymers 0.000 claims description 20
- 229960005070 ascorbic acid Drugs 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 18
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims description 16
- 229930003268 Vitamin C Natural products 0.000 claims description 16
- 235000010323 ascorbic acid Nutrition 0.000 claims description 16
- 239000011668 ascorbic acid Substances 0.000 claims description 16
- 235000019154 vitamin C Nutrition 0.000 claims description 16
- 239000011718 vitamin C Substances 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 15
- 150000001412 amines Chemical class 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 13
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 12
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 239000003638 chemical reducing agent Substances 0.000 claims description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 5
- 229930003799 tocopherol Natural products 0.000 claims description 5
- 239000011732 tocopherol Substances 0.000 claims description 5
- 102000004190 Enzymes Human genes 0.000 claims description 4
- 108090000790 Enzymes Proteins 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- PZYDAVFRVJXFHS-UHFFFAOYSA-N n-cyclohexyl-2-pyrrolidone Chemical compound O=C1CCCN1C1CCCCC1 PZYDAVFRVJXFHS-UHFFFAOYSA-N 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 claims description 4
- 229940103494 thiosalicylic acid Drugs 0.000 claims description 4
- 235000010384 tocopherol Nutrition 0.000 claims description 4
- 229960001295 tocopherol Drugs 0.000 claims description 4
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 claims description 4
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 claims description 3
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 3
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 3
- PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 claims description 3
- 229940074391 gallic acid Drugs 0.000 claims description 3
- 235000004515 gallic acid Nutrition 0.000 claims description 3
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 230000000269 nucleophilic effect Effects 0.000 claims description 3
- 125000000962 organic group Chemical group 0.000 claims description 3
- 150000002923 oximes Chemical class 0.000 claims description 3
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 3
- 150000003573 thiols Chemical class 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- DCALJVULAGICIX-UHFFFAOYSA-N 1-propylpyrrolidin-2-one Chemical compound CCCN1CCCC1=O DCALJVULAGICIX-UHFFFAOYSA-N 0.000 claims description 2
- PYQVCYCHUWIDIS-UHFFFAOYSA-N 2,5,7,8-tetramethyl-3,4-dihydro-2h-chromen-6-ol Chemical compound OC1=C(C)C(C)=C2OC(C)CCC2=C1C PYQVCYCHUWIDIS-UHFFFAOYSA-N 0.000 claims description 2
- ORIHZIZPTZTNCU-VMPITWQZSA-N 2-[(E)-hydroxyiminomethyl]phenol Chemical compound O\N=C\C1=CC=CC=C1O ORIHZIZPTZTNCU-VMPITWQZSA-N 0.000 claims description 2
- GBHCABUWWQUMAJ-UHFFFAOYSA-N 2-hydrazinoethanol Chemical compound NNCCO GBHCABUWWQUMAJ-UHFFFAOYSA-N 0.000 claims description 2
- QPHPUQJVKQXISS-UHFFFAOYSA-N 4-oxo-4-sulfanylbutanoic acid Chemical compound OC(=O)CCC(S)=O QPHPUQJVKQXISS-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 2
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 claims description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- 125000005157 alkyl carboxy group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims description 2
- 235000018417 cysteine Nutrition 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 claims description 2
- 229940067157 phenylhydrazine Drugs 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical group OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- RSBHKNDSJJBCMN-UHFFFAOYSA-N 1-(1-hydroxyethyl)pyrrolidin-2-one Chemical compound CC(O)N1CCCC1=O RSBHKNDSJJBCMN-UHFFFAOYSA-N 0.000 claims 1
- RUECCIUIKFVPPR-UHFFFAOYSA-N 1-(1-hydroxypropyl)pyrrolidin-2-one Chemical compound CCC(O)N1CCCC1=O RUECCIUIKFVPPR-UHFFFAOYSA-N 0.000 claims 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 claims 1
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims 1
- VJQVYOWJNOGOIO-UHFFFAOYSA-N C(C)[C-]1NC=CC1=O Chemical compound C(C)[C-]1NC=CC1=O VJQVYOWJNOGOIO-UHFFFAOYSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims 1
- FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 claims 1
- 239000004698 Polyethylene Substances 0.000 claims 1
- 241000219000 Populus Species 0.000 claims 1
- 241000270666 Testudines Species 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- KZNMRPQBBZBTSW-UHFFFAOYSA-N [Au]=O Chemical compound [Au]=O KZNMRPQBBZBTSW-UHFFFAOYSA-N 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 claims 1
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 claims 1
- 239000003098 androgen Substances 0.000 claims 1
- 229940030486 androgens Drugs 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000005026 carboxyaryl group Chemical group 0.000 claims 1
- 229930003836 cresol Natural products 0.000 claims 1
- 238000004132 cross linking Methods 0.000 claims 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 238000000855 fermentation Methods 0.000 claims 1
- 230000004151 fermentation Effects 0.000 claims 1
- 229910001922 gold oxide Inorganic materials 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 229960000485 methotrexate Drugs 0.000 claims 1
- XKLJHFLUAHKGGU-UHFFFAOYSA-N nitrous amide Chemical compound ON=N XKLJHFLUAHKGGU-UHFFFAOYSA-N 0.000 claims 1
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- SSOLNOMRVKKSON-UHFFFAOYSA-N proguanil Chemical compound CC(C)\N=C(/N)N=C(N)NC1=CC=C(Cl)C=C1 SSOLNOMRVKKSON-UHFFFAOYSA-N 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 claims 1
- 229910052815 sulfur oxide Inorganic materials 0.000 claims 1
- VYSYZMNJHYOXGN-UHFFFAOYSA-N ethyl n-aminocarbamate Chemical compound CCOC(=O)NN VYSYZMNJHYOXGN-UHFFFAOYSA-N 0.000 description 10
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- JEAWPIKEEQZLJQ-UHFFFAOYSA-N 1h-benzimidazol-2-yl(phenyl)methanol Chemical compound N=1C2=CC=CC=C2NC=1C(O)C1=CC=CC=C1 JEAWPIKEEQZLJQ-UHFFFAOYSA-N 0.000 description 7
- GZLYSDJGEXGQDO-UHFFFAOYSA-N C1=CC=CC2=NCNC=C21 Chemical compound C1=CC=CC2=NCNC=C21 GZLYSDJGEXGQDO-UHFFFAOYSA-N 0.000 description 7
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 6
- 230000005764 inhibitory process Effects 0.000 description 6
- DLDJFQGPPSQZKI-UHFFFAOYSA-N but-2-yne-1,4-diol Chemical compound OCC#CCO DLDJFQGPPSQZKI-UHFFFAOYSA-N 0.000 description 5
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 5
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 4
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 230000005611 electricity Effects 0.000 description 4
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 4
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 4
- 229910052721 tungsten Inorganic materials 0.000 description 4
- 239000010937 tungsten Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 229930003427 Vitamin E Natural products 0.000 description 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 3
- 150000001335 aliphatic alkanes Chemical group 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229940015043 glyoxal Drugs 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229940046009 vitamin E Drugs 0.000 description 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 2
- XNMQEEKYCVKGBD-UHFFFAOYSA-N 2-butyne Chemical compound CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 2
- RWHQMRRVZJSKGX-UHFFFAOYSA-N 2-oxobutanal Chemical compound CCC(=O)C=O RWHQMRRVZJSKGX-UHFFFAOYSA-N 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 235000013405 beer Nutrition 0.000 description 2
- 235000021028 berry Nutrition 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 230000002079 cooperative effect Effects 0.000 description 2
- XVOYSCVBGLVSOL-UHFFFAOYSA-N cysteic acid Chemical compound OC(=O)C(N)CS(O)(=O)=O XVOYSCVBGLVSOL-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229940079877 pyrogallol Drugs 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- RLNWRDKVJSXXPP-UHFFFAOYSA-N tert-butyl 2-[(2-bromoanilino)methyl]piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CNC1=CC=CC=C1Br RLNWRDKVJSXXPP-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 2
- 235000019165 vitamin E Nutrition 0.000 description 2
- 239000011709 vitamin E Substances 0.000 description 2
- HDKLIZDXVUCLHQ-BQYQJAHWSA-N (3E)-3-nonen-2-one Chemical compound CCCCC\C=C\C(C)=O HDKLIZDXVUCLHQ-BQYQJAHWSA-N 0.000 description 1
- HDKLIZDXVUCLHQ-UHFFFAOYSA-N (E)-3-Nonen-2-one Natural products CCCCCC=CC(C)=O HDKLIZDXVUCLHQ-UHFFFAOYSA-N 0.000 description 1
- RDOUKLWMBUMPIX-UHFFFAOYSA-N 1-(cyclohexen-1-yl)propan-2-one Chemical compound CC(=O)CC1=CCCCC1 RDOUKLWMBUMPIX-UHFFFAOYSA-N 0.000 description 1
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 description 1
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 description 1
- RJKGJBPXVHTNJL-UHFFFAOYSA-N 1-nitronaphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=CC2=C1 RJKGJBPXVHTNJL-UHFFFAOYSA-N 0.000 description 1
- IKKUKDZKIIIKJK-UHFFFAOYSA-N 2,2-diethoxyethanol Chemical compound CCOC(CO)OCC IKKUKDZKIIIKJK-UHFFFAOYSA-N 0.000 description 1
- UHZLTTPUIQXNPO-UHFFFAOYSA-N 2,6-ditert-butyl-3-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1C(C)(C)C UHZLTTPUIQXNPO-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- LCRCBXLHWTVPEQ-UHFFFAOYSA-N 2-phenylbenzaldehyde Chemical compound O=CC1=CC=CC=C1C1=CC=CC=C1 LCRCBXLHWTVPEQ-UHFFFAOYSA-N 0.000 description 1
- AZQSINYIKQSHFR-UHFFFAOYSA-N 4,4,4-trihydroxybutanoic acid Chemical compound OC(=O)CCC(O)(O)O AZQSINYIKQSHFR-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- ICGLPKIVTVWCFT-UHFFFAOYSA-N 4-methylbenzenesulfonohydrazide Chemical compound CC1=CC=C(S(=O)(=O)NN)C=C1 ICGLPKIVTVWCFT-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 101100314273 Arabidopsis thaliana TOR1 gene Proteins 0.000 description 1
- ZETHHMPKDUSZQQ-UHFFFAOYSA-N Betulafolienepentol Natural products C1C=C(C)CCC(C(C)CCC=C(C)C)C2C(OC)OC(OC)C2=C1 ZETHHMPKDUSZQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004255 Butylated hydroxyanisole Substances 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
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- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- ULBBXWVIXXPSOD-UHFFFAOYSA-N N-cyclohexylpyrrolidine Chemical compound C1CCCN1C1CCCCC1 ULBBXWVIXXPSOD-UHFFFAOYSA-N 0.000 description 1
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical compound CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
- 206010041349 Somnolence Diseases 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- DJSISFGPUUYILV-UHFFFAOYSA-N UNPD161792 Natural products O1C(C(O)=O)C(O)C(O)C(O)C1OC(C(=C1O)O)=CC2=C1C(=O)C=C(C=1C=CC(O)=CC=1)O2 DJSISFGPUUYILV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 235000020958 biotin Nutrition 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- HBBRVEMMVUOSTL-UHFFFAOYSA-N butyl n-aminocarbamate Chemical group CCCCOC(=O)NN HBBRVEMMVUOSTL-UHFFFAOYSA-N 0.000 description 1
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
- 229940043253 butylated hydroxyanisole Drugs 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- NPLTVGMLNDMOQE-UHFFFAOYSA-N carthamidin Natural products C1=CC(O)=CC=C1C1OC2=CC(O)=C(O)C(O)=C2C(=O)C1 NPLTVGMLNDMOQE-UHFFFAOYSA-N 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- IAQRGUVFOMOMEM-ARJAWSKDSA-N cis-but-2-ene Chemical compound C\C=C/C IAQRGUVFOMOMEM-ARJAWSKDSA-N 0.000 description 1
- SGNMNJRAIJNULS-UHFFFAOYSA-N cyclohexene;propan-2-one Chemical compound CC(C)=O.C1CCC=CC1 SGNMNJRAIJNULS-UHFFFAOYSA-N 0.000 description 1
- 208000002925 dental caries Diseases 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- HEOKFDGOFROELJ-UHFFFAOYSA-N diacetal Natural products COc1ccc(C=C/c2cc(O)cc(OC3OC(COC(=O)c4cc(O)c(O)c(O)c4)C(O)C(O)C3O)c2)cc1O HEOKFDGOFROELJ-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- XZBIXDPGRMLSTC-UHFFFAOYSA-N formohydrazide Chemical compound NNC=O XZBIXDPGRMLSTC-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 150000004820 halides Chemical group 0.000 description 1
- 239000011874 heated mixture Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229960004337 hydroquinone Drugs 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- ARZLUCYKIWYSHR-UHFFFAOYSA-N hydroxymethoxymethanol Chemical class OCOCO ARZLUCYKIWYSHR-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- DMJNNHOOLUXYBV-PQTSNVLCSA-N meropenem Chemical compound C=1([C@H](C)[C@@H]2[C@H](C(N2C=1C(O)=O)=O)[C@H](O)C)S[C@@H]1CN[C@H](C(=O)N(C)C)C1 DMJNNHOOLUXYBV-PQTSNVLCSA-N 0.000 description 1
- 229940032713 merrem Drugs 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- HKEBYUNPANBGPL-UHFFFAOYSA-N nona-2,4-diene Chemical compound CCCCC=CC=CC HKEBYUNPANBGPL-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000011941 photocatalyst Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- KZGIAZNSUAVEDJ-UHFFFAOYSA-N propane;propan-2-ol Chemical compound CCC.CC(C)O KZGIAZNSUAVEDJ-UHFFFAOYSA-N 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- DJSISFGPUUYILV-ZFORQUDYSA-N scutellarin Chemical compound O1[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1OC(C(=C1O)O)=CC2=C1C(=O)C=C(C=1C=CC(O)=CC=1)O2 DJSISFGPUUYILV-ZFORQUDYSA-N 0.000 description 1
- 229930190376 scutellarin Natural products 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 125000002640 tocopherol group Chemical class 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/42—Stripping or agents therefor
- G03F7/422—Stripping or agents therefor using liquids only
- G03F7/425—Stripping or agents therefor using liquids only containing mineral alkaline compounds; containing organic basic compounds, e.g. quaternary ammonium compounds; containing heterocyclic basic compounds containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/264—Aldehydes; Ketones; Acetals or ketals
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3218—Alkanolamines or alkanolimines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/34—Organic compounds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)
- Detergent Compositions (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Treatment Of Water By Oxidation Or Reduction (AREA)
Description
267186 五、發明説明(1 )IOOOL 本發明係關於包含遢原劑的鹸性光阻材料汽提姐成物' 及這種汽提姐成物在從包栝金鼷如鎢以及/或铜和其鋁合 金的基Η上剝離光阻材料時用Μ減少或抑制金靨腐蝕以及 /或金矚損失的用途。 經濟部中央標準局員工消費合作社印製 微雷子產品製造的一個主要部份是使用光阻材料將面罩 或標線的围像移轉到所需要的基Η電路層。在完成所需的 圖像移轉之後,就要除去光阳材料,也就是說在進行某種 隨後製稈步驟前要將該材料自基Η汽提。大約在19 80年開 始,醮胺和醣胺與各種共溶劑的混合物平常即被用在這種 汽提步驟,請參閲,例如Ward等人的美國專利4,395,479 、4,428,871 K 及 4,401,748 。 當光阴材料仍在基Η上時,視所進行的加工處理方式而 定,光阳材料聚合物可能會交聯或硬化到某種程度Μ致於 醮胺基溶劑不再有效地汽提光阳材料。大約從1985年開始 ,即使用含有額外驗性成份如有機胺類(請參見Johnson 的美國專利4,592,787 ,Merrem的美國專利4,765,844 , Sizensky的美國專利 4,617,251 * Turner的 W0 87/05314 W及Thomas等的美國專利4,791,043)或是氫氧化第四銨( 參見516口{>3^等的美國專利4,776,892,1|£^的美國專利 4,744,834 ,Mqrtin 的 W0 88/05813 )的胺類混合物 Μ 便利 此等硬化光陏材料之去除。 ---------1^-- (請先聞讀背面之注意事項再填寫本頁) -5 本紙張尺度適用中國國家橾準(CNS ) Α4规格(210Χ297公釐) 經濟部4-央揉準局貝工消費合作社印製 267188 五、發明説明(2 ) 在用於包含金_,特別是鎢或者是網以及_、鋁合金的 微雷路上的汽提劑中使用這呰鹼性成份可能會等致金鼷損 失。在使用這些驗性汽提劑時,曾發現到各種形式的金臛 腐蝕例如腐蝕鬚、金匾線凹痕或針孔。在鎢和銅的情形時 由於溶解的氧提供陰橘反應而可能會在加熱之無水有機汽 提姐成物混合物中發生腐蝕。 因此非常需要能夠提供適合於從含有金顧的基片上汽提 交聯或硬化光阴材料聚合物而金靨腐蝕Μ及/或金覊損失 減少或受到抑制之含鹼性光阴材料汽提劑姐成物。本發明 的進一步目的是提供一種從含金屬基片上汽提交聯或硬化 光闲材料方法,其係使用含有化學藥劑Μ減少或抑制金鼷 腐蝕或金驅損失的含鹼性光阳材料汽提姐成物。 現已發現在含鹼性光阻材料汽提姐成物中加入某些選原 酬即會產生可減少/或抑制金鼷腐蝕以及/或金驅損失的 光阴材料汽提姐成物,當這棟姐成物用於自含金靨基Η上 除去交聯或硬化光阳材料時。適合用在本發明含鐮性光阻 材料汽提姐成物的湛原劑有下列各種:抗壊血酸(維生素 C ) 、丁炔二酵、不飽含酮、腺酸、四咪唑、胼和其衍生 物包栝阱基甲酸酯(二胺腺酯)、肟、對苯二酚、連苯三 酚、五倍子酸、2,4,5三羥基丁醢笨、生育酚(維生素 Ε>、6-羥基-2,5,7,8-四甲基色滿-2-羧酸、丁基化羥基 甲笨(ΒΗΤ) 、丁基化羥基苯甲醚(ΒΗΑ) 、2,6 -二-第三- -5 - 本紙張尺度適用中國國家標率(CNS ) Α4規格(210X 297公釐) -------^---1^.-- (請先閲讀背面之注意事項再填寫本頁) ,ιτ 267186 經濟部中央橾準局貝工消費合作社印褽 五、發明説明(5 ) 丁某-4-珲甲基酚、硫醇、水楊醛、4_羥基笨甲醛和乙二 醇醛二烷基縮醛Μ及其混合物。本發明光阻材料汽提姐成 物中所用堪原劑的量為能有效減少或抑制金靨腐蝕或金鼷 損失的仟何最,而該最一般將在約〇1)Κ到約10¾的範_内 ,此係Μ光阳材料汽提姐成物的總重量為準。 發~5〇5-^钿銳明 本發明的改良防金鼷腐蝕光陏材料汽提姐成物包含有機 溶劑系統、鐮性成份和至少一種適用的還原劑。本發明光 阳材料汽提婼成物中使用的有機溶劑系統通常是一種具有 從大約8到約15的溶解度參數的糸統,該參數是由三個 Hansen溶解度參數(分散性,極性,和氫鐽)的平方和開 平方所得到的。而該溶劑糸統可以包含一些個別溶劑的任 何一棟或者是數種不間溶劑的混合物。這類溶劑可提及的 例子,有各棟吡咯烷齲化合物諸如2-吡咯烷酮、1-甲基2 吡咯烷酮、1-乙基2吡咯烷酮、1-丙基2吡咯烷酮、卜羥 乙基遇氣化2吡咯烷酮、1-羥丙基2吡咯烷酮、正環己基 吡咯焼_等等;三-或二乙二酵單烷基醚,諸如具化學式 HtHCfUCH —bR者其中R是含1至4個碳原子的烷基而x 0 是2或3;含硫氣的化合物諸如具化學式Ri-1-R2之二烷基li 〇 礓其中R1及R2為1至4個碳原子的烷基,二甲亞砸;具化學 式 本紙張歧適用中1|困家橾準(CNS )从魏_ ( 21GX297公羡) (請先聞讀背面之注意事磅再填寫本頁) Γ -裝' 訂 S67186 A7 B7 五、發明説明(4)
R3 經濟部中央揉準局員工消费合作社印製 之 1 , 1 二 其中R3是 播和乙基 甲蓽甲醯 成物窜最 本發明 構形式。 --氮取代 和pKa值 可K 一提 、1 -胺某 酵、2- < 1 - ( 2 -胺 是它的親 用最是從 30% ° 本發明 氧有效的 氧化-四氫嗶盼的化合物 氧、甲基或乙基例如四亞甲基通、甲 四亞甲基砸;K及聚乙二酵、二甲基 胺。本發明汽提劑姐成物中之瑢劑部 的約50¾:至約98¾,較佳為約70至90重 可Μ使用的鹸性汽提姐成物也涵蓋廣 它們的離解常數M PKa的數值表示, 胺的約9至11,至第二胺嗎福啉和羥 略低的羥基胺衍生物。在可以使用的 及的有親核性胺類,較佳實例如卜胺 -3-丙酵、2-< 2 -胺乙氧基)乙酵、 2-胺乙胺基)乙醇、2-(2-胺乙胺基 乙* )六氧吡畊等等。比胺實際PKa 核件必需很高。本發明汽提組成物中 紺成物電最的約U到約50« ,較佳為 基四亞甲基 乙豳胺或二 份通常占姐 最%。 大種類的結 自/3 -氧或 基胺的8 . 3 鹼性成份中 基-2-丙酵 2-胺基-乙 )乙胺、 值更重要的 胺成份的使 約10¾至約 改良光陌材料姐成物中可用作為堪原劑而對清除 逋原劑有下列各種: 本紙張尺度逋用中國國家搮準(CNS ) A4規格(210 X 297公釐) (請先閲讀背面之注意事項再填寫本頁) 267186 A7 B7 五、發明説明( 含反應性多鍵的化合物,即,抗壞血酸(維生素c)*腯 酸,丁炔二醇,不飽和酮類諸如環己烯基丙酮和3 -壬烯 -2-酮、Μ及四咪呻; 肼和其衍生物,即,具化學式R4-NH-NH2的化合物,其 中1是氣或有機基,較佳是氣原子,甲醮基,烷基,氧碳 酸某,鞸烷基,烷羧基或芳基例如苯基; 肟類: 可輕易氧化的芳香族 酚,連苯三酚,五倍子 E>,6-羥某-2,5,7,8-四甲基色滿(p兔《) -2-羧酸,丁基 化羥蓽甲 -4 -經蓽 化學式 化合物和氧化抑制劑,即,對苯二 酸和它的烷酯類,生育酚(維生素 苯、丁基化羥基甲醚Μ及2,6 -二-第三-丁基 甲基酚: RBSH的碕酵類其中Re是有機基諸如雜環基,羧芳 經濟部中央榡準局貝工消費合作社印製 基,二羧 其中1?8和 醛及其 二烷基縮 的烷某一 子,更样 本發明 生素C ), -2-網, R7是烷基;和 衍生物,即, 薛,特別是乙 般是1至12個 為1至4個碳原 汽提組成物中 腺酸,2-丁炔 2,3, 5,6-四氫 0 羧烷基或者化學式Re-〇-i-R7-的基 水楊醛,4-羥基苯甲醛和乙二酵醛 二醇醛二乙基縮醛。前述還原劑中 碳原子之烷基,較佳為1至6涸碳原 子之烷基。 使用的特佳堪原劑有抗壞血酸(維 -1,4二酵,1-環己烯丙酮,3-壬烯 -6-笨咪唑基[2,Ι-b]噻唑和其氫
(CNS ) A4規格(210X297公釐) (請先聞讀背面之注意事項再填寫本頁)
267186 A7 £7_ 五、發明説明(6 ) (請先闖讀背面之注$項再填寫本頁) 氛化物,阱,對-甲苯磺醣基醸肼,甲酸醣肼,願丁烯二 胼,肼水合物,羥乙基胼,苯阱,阱基甲酸第三丁基酯, 阱蓽甲酸乙酯,水楊醛眄,丙酮肟,連笨三酚,五倍子酸 ,2,4,5三羥萆T醣苯,3,5-二-第三-丁基-4-羥基甲 苯,3-第三-丁基-4-羥基笨甲醚,2,6-二-第三-丁基 -4-羥甲基酚,生育酚(維生素E),6-羥基-2,5,7,8四甲 某色滿(〇兔> -2-羧酸,2-氫硫基_4[3H]1,3-二-氮雜萘 ,+二烷氧碲基丙酸酯,硫水楊酸,氫碲基丁二酸,半胱 氨酸,2 -氫硫箪苯並嗶啤,水楊醛,4 -羥苯醛和乙二酵醛 二乙蓽縮醛。 本發明遢原劑在含鹼性汽提姐成物中的使用量應能有效 減少或抑制金靨腐蝕或金驅損失,且一般是在組合物總重 最的約0· 1¾到約10¾ ,較佳自約0. IX到5¾,更佳約0. 15K到 3X,而最佳約U到3¾之範圍内。 本發明的汽提姐成物可有效的汽提很多各種不同的光阻 材料,特別是正光阳材料。大部份的光阻材料都是由鄰萘 醞《氮磺酸酯或醮胺感光劑或光活性成份,加上酚醛樹腊 ,可溶酚醛樹脂,聚丙烯醯胺或丙烯酸聚合物種類的结合 劑或樹_所驵成。這些光阻材料都是此類技藝中已熟知者 。此類光阳材料和感光劑在下列的美國專利中都有說明: 經濟部中央橾準局貝工消費合作社印製 3,046,118; 3,046·121; 3,106,465; 3,201,239; 3,538,137; 3,666,473; 3,934,057; 3,984,582和 4,007,047 。本發明汽提組成物可用之光阻材料姐成物可
提及的例子如次:0CG微雷子材料糸列^^-6,HiPR -9 - 本紙張尺度逋用中國國家標準(CNS ) A4规格(210X297公釐) 267186 五、發明説明(7 ) 6500, HPR500, OCG 825, OCG 895, OCG 897 和OiR 32的 光阳材料,Hoechst Celanese糸列 AZ 1500, 6100, 6200B, 7500, 7500T, DX, P4000 和 PF 500的光阻材料; Shipley 公司的Megaposit S1400, S1800, S3800, SPR2. SPR500-A 和 SPRT500-A 光姐材料;Morton 電子材料 的EL-,H0VAW及0FPR-系列光阻材料;Toray工業的 EBR-9;還有I丨CB-JSR雷子的PFR-系列光姐材料。 本發明汽提姐成物的改良性質將在下列各實例中說明。 在實例中,已加人本發明《原劑的含驗性溶劑糸統汽提劑 钼成物是下列A到0的姐成物: (請先閱讀背面之注意事項再填寫本頁) -裝. 訂 經濟部中央標準局員工消費合作社印製 ο 11 本紙張尺度適用中國國家棣準(CNS > A4规格(2丨0><297公釐) 267186 五、發明説明(8 ) 組成—物成ja—1重1份丄 ______— ή 二甲苺甲釀胺(90) + 2-胺基乙酵(10) Β 二甲基乙醢胺(90) + 2-胺基乙酵(10) C 二甲苺乙醢胺(90)+1-胺基-3-丙酵(10) D 二甲*乙醢胺(90) + 1-胺基-2-丙醇(10) E 二甲基乙釀胺(60) + 1-胺基-2-丙酵(10) +四亞 甲基砸(30> F 正-甲基遇氫化吡咯瑁_(60) +卜胺基-2-丙酵 (10> +正-環己基吡咯烷酮(30) G TF.-甲基吡咯烷嗣(70) + 1-胺基-2-丙醇(30) Η 正_甲基吡咯烷酮(90) + 2-(2 -胺乙胺基)乙酵 (10) I 二甲基亞通(90)+1-( 2 -胺乙基六氫吡畊)(10> j 正-.甲基吡咯烷酮(80) + 2- ( 2 -胺乙胺基)乙酵 (1 0 ) + ΪΗ - ( 2 -羥乙基)吡咯烷酮(1 0 > K 7F -甲*吡咯烷酮(70)+2-( 2 -胺乙胺基)乙酵 (10) +三乙二酵單甲基醚(20) L TF-甲基吡咯烷酮(60)+2-( 2 -胺乙胺基)乙酵 (10) +二乙二酵單乙基醚(3〇) M 二甲*亞碾(70) +卜胺基-2-丙酵(30> 經濟部中央揉準局員工消費合作社印製 (請先閲讀背面之注意事項再填寫本頁) Ν 正-甲基吡咯烷酮(50)+2-( 2 -胺乙氧基)乙酵 (+40)+四亞甲基躐(1〇) 〇 正-甲蓽吡咯垸酮(60) +卜胺基-2-丙酵(10) + 四亞甲基磲(30> 本紙張尺度適用中國國家揉準(CNS ) A4規格(210x297公釐) 經濟部中央橾準局貝工消費合作社印製 267186 a? ._____B7 五、發明説明(9 ) W上含鏡性汽提劑組成物的腐蝕速率係以加和不加堪原 商丨谁行澜最*然後計算本發明汽提組成物的腐蝕抑制百分 比。腐蝕速率係使用了下列三種方法測最: 方法 1 : 將超遇99.9%鎢的試料(〇.〇5x12x50毫米)放在丙酮中 清洗’乾燦後秤電。然後將試料放在加入及不加入遨原劑 的上述一棟驗件测試姐成物(加上u水來加重腐蝕)中加 熱。存8 5 t下浸沒於測試姐成物中4小時後取出試料,以 丙_清洗,乾燥並秤爾。將電最的損失轉換成腐蝕速率, 最後梅算成所用遇原劑的抑制百分比。 方法2 : 和方法1相同除了試料是超遇99 98!(;的铜(0 〇25χ12χ 50毫米) 方法 3 : 將網試料(0.05 x 10 x 30毫米}放在異丙醇中清洗、乾煉 然後在10毫升汽提組成物中在8〇Ί〇下加熱1小時。飼然後 Μ原子吸收光謅測最澜試溶液吸收之銅量並換算成所用堪 原酬的抑制百分比。 使用上述三個方法測最的汽提姐成物Α到〇 (無本發明堪 原劑 > 的腐蝕速率Μ每小時埃表示列示於下。结果如下: -12 - 本紙張尺度適用中國國家揉率(CNS ) Α4规格(210Χ297公羞) ' 一— -- (請先閲讀背面之注意事項再填寫本頁) -裝. *11 267186 五、發明説明(10) A7 B7 組―成―物 A B C D E F G Η I J K L Μ N 0 方後— 1 1 1 1 1 2 2 2 2 2 2 2 2 3 3 埃/小時鏞 38 120 58 110 100 埃/小時緬 390 450 590 170 260 230 150 730 430 860 (請先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局負工消費合作社印製 然後將本發明的遇原劑加到上述汽提組成物中,並Μ上 述三揷方法之一來進行測最腐蝕損失。然後根據下列公式 計算腐蝕損失的抑制百分比: 使用遒原劑的腐蝕速率 抑制百分比=1 0 0 ( 1 不使用邐原劑的腐蝕速率 13 本紙張尺度適用中國國家標準(CNS ) Α4规格(210Χ297公釐) 267186 A7 B7五、發明説明(11 ) S 例上述含鹼性汽提姐成物A到0中加人本發明通原劑即產生 下列抑制结果: 經濟部中央標準局貝工消费合作社印製 測 試 汽 提 遒 原 劑 (加入 的 金 羼 損失抑 方 法 絹 成物 窜 最 百 分 ,% ) 制 丙 ^ hh . 1 A 抗 壊 血 酸 (維 生 素 C) (1) 100 1 B 2- 丁 炔 -1 ,4- 二 醇 (2) 79 1 B 腺 酸 (3) 94 1 B 1 - 環 己 烯 基丙_ (5) 92 2 F 抗 壊 血 酸 (維 生 素 C ) (2) 90 2 Η 抗 壞 血 酸 (維 生 素 C) (2) 100 2 Η 3- 壬 烯 -2 _ _ (10) 93 2 I 抗 壊 血 酸 (維 生 素 C) (2) 62 2 J 抗 壞 血 酸 (維 生 素 C) (2) 67 2 K 抗 壊 血 酸 (維 生 素 C) (2) 72 2 L 抗 壞 血 酸 (維 生 素 C) (2) 57 3 0 抗 壞 血 酸 (維 生 素 C ) (0.1) 91 3 0 抗 壞 血 酸 (維 生 素 C) (0.5) 98 3 0 抗 壞 血 酸 (維 生 素 C) (1) 97 3 N 抗 壊 血 酸 (維 生 素 C) (0.1) 92 3 H 抗 壞 血 酸 (維 生 素 C) (1 ) 92 3 0 四咪唑鹽酸 鹽 (1) 91 -14 - 本紙張尺度適用中國國家標準(CNS > A4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁) -裝· 訂 A7 B7 五、發明説明(12 ) 經濟部中央標準局貝工消費合作社印製 測試 汽提 還原劑(加入的 金鼷損失抑 方法 姐成物 電 最 百 分 比 %) 制苒分hh 3 0 *四咪啤 (1 ) 63 1 Β 對 - 甲 笨 m 基 m 肼 (2) 75 1 A 甲 酸 醯 肼 ⑴ 100 1 C 阱 (0 .5) 100 1 D 阱 (0 .1 ) 64 1 D 胼 (2) 87 1 B 順 丁 烯 醸 肼 (2) 62 3 0 阱 水 合 物 (1) 99 3 0 肼 水 合 物 (0 .1 ) 98 3 0 η 乙 基 阱 (1) 99 3 0 苯 肼 (1) 98 3 0 肼 基 甲 酸 第 三 丁 基 酯 (1 ) 97 3 0 甲 酸 醯 胼 (1) 96 3 0 肼 基 甲 酸 乙 酯 (1 ) 97 3 0 對 甲 笨 砸 基 醸 胼 (1 ) 98 3 N 胼 水 合 物 (1 ) 96 1 B 水 楊 醛 肟 (5) 87 1 B 丙 酮 肟 (5) 78 1 B 對 苯 二 酚 (1 ) 100 1 E 對 苯 二 酚 (1 ) 82 2 F 連 笨 三 酚 (1 ) 63 -15 - (請先閲讀背面之注意事項再填寫本頁)
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、1T 本紙張尺度速用中國國家標準(CNS ) Α4規格(210Χ297公釐) 經濟部中央標準局員工消費合作社印製 267ΐ8β 五、發明説明(15 ) 測 試 汽提 « 原 劑 (加入的 金 鼷 損失抑 方 法 組肢物 霞 最 百 分 hh - %) 制 百 分比, 2 G 五 倍 子 m (3 ) 68 3 0 對 苯 二 m (0 .1 ) 95 3 0 對 笨 二 m (0 .5) 95 3 0 對 苯 二 酚 (1 ) 96 3 N 對 苯 二 酚 (1) 87 1 B ΒΗΤ (3) 77 1 B 維 生 素 E (生育酚> (1) 54 1 B «e Τ Γ 0 1 〇 X (1) 72 1 C 2- 氫 硫 基 -4 (3H) 1, 3- 二 氮 雜 萘 (3) 86 1 D 十 二 烷 氫 硫基丙酸 酯 (5) 100 2 G 硫 水 楊 酸 (3) 91 2 G 氫 硫 基 丁 二酸 (3) 72 2 Μ 半 胱 氛 酸 (3) 68 3 0 2- m 硫 基 -4 [ 3 Η ] 1 , 3- 二 氮 雜 萘 (1 ) 86 3 0 2- m 硫 基 -4 [3Η] 1 , 3- 二 氮 雜 萘 (5) 89 3 0 2- 氫 碕 基 -苯駢晖 唑 (5) 95 3 Ν 2- 氣 硫 基 -4 [3Η]1, 3- —. 氮 萘 (1 ) 88 -16 - (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家橾率(CNS ) A4規格(210X297公釐) 267186 A7 B7 五、發明説明(u ) 測試 汽提 方法_組_虛_物1
遒原劑(加入的 重畺百分hh,SO 金屬損失抑 制百分hh,% 1 D 水楊醛 (5) 62 1 Β 乙二醇醛 二 乙 基縮醛 (5) 81 1 Β 4 -釋基- 苯 甲 醛 (5 ) 61 * ”四咪啤"=2,3,5,6 -四氣-6-笨咪唑基[2, Pb]噻唑。 ** ” BHT” =3,5 -二_ 第三-丁基-4-羥甲苯。 *** ”1>〇丨(^”=6-羥基-2,5,7,8四甲基色滿-2-羧酸。 從Μ上本發明的說明,熟諸此藝者將明白本發明可作各 棟修IF.而不偏離其精神。因此•本發明的範圍並無意僅限 於所列舉及說明的特定實例。 (請先閱讀背面之注意事項再填寫本頁)
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•-Q 經濟部中央標準局員工消費合作社印製 17 本紙張尺度逍用中國國家標率(CNS ) Α4規格(210X297公釐〉
Claims (1)
- 公告本 第83109330號專利申請案 ,AQ Qi Q A« 中文申請專利範圍修正本(84^^^ __ D8 六、申請專利範圍 267186 1 · 一種含鹼性光阻材料汽提姐成物,其包含50¾至98重 量%具溶解度參數8至15之汽提溶劑* 1¾至50重量% 的親核性胺和堪原劑,其量懕在該汽提組成物用K自 含金臛的基片上剝除硬化或交聯光阻材料時能有效抑 制或減少金羼腐蝕,該還原劑選自抗壞血酸(維生素 C),不飽和_,脲酸和四咪哇,阱和其衍生物(選自 化學式R4-NH-NH2者,其中R4是氫或選自甲藤基,烷 基,氧羰基,羥烷基,烷羧基或芳基的有機基),肟 (選自水楊醛肟和丙酮肟)、2,3,5,6-四氫-6-苯眯唑 基[2,1-b]噻唑和其氫氯化物(鹽酸鹽),對苯二酚 、五倍子酸,2,4,5-三-羥基丁醯苯,3,5 -二-第三 -丁基-4-羥基甲苯,3-第三-丁基-4-羥苯甲醚, 2,6-二-第三-丁基-4-羥基甲酚,生育酚(雄生素 E) * 6 -羥基-2, 5 ,7,8-四甲基色滿(。龟)-2-羧酸、硫 醇(選_自具化學式RSSH的化合物,其中Rs是選自雜環 ,羧芳基,二羧烷基,胺基取代羧烷基或 0 II 具化學SRe-〇-C-R7-的基(其中ΚΙΟΙΤ是烷基}之有 ------------「訂 d丨線 (請先間讀背面之注意事項再塡寫衣頁) 烴濟部中夾饽爭曷員工消費合作社印製 2 } 乙 基和 機薛 其 及 0 醛 酵 >物 甲-合 苯提 基Μ 羥所 述 4-上 > 中 醛其 楊及 水Μ ΓΓΠ » 選醛Μ縮 Μ基 生烷 桁:fc 基。 烷進 之基 子為 原量 碳重 個的 12物 1 到成第 1姐圍 有提範 具汽利 是M專 基皆請 垸比申 的分據 中百根 量 重 中 其 成 組 提 汽 料 材 阻 光 性 0 含 的 項 藤 及基 酮碾 丙苯 基甲 烯- 己對 環, 1-肼 白白 選選 係係 劑劑 原原 還還 酮肼 和 * 飽 _ 不-中-2 其烯 *壬 物3- 裎濟.91·φ,央準局KX工消費合作社印¾ 267186 as8 C8 _ D8 _六、申請專利範圍 肼,甲藤肼,順丁基二酸醸肼,肼水合物,羥乙基肼 ,苯肼,肼基甲酸第三丁基酯及肼基甲酸乙酯,硫酵 還原劑係選自2 -氫碲基-4[3H]晻唑啉,十二烷氫硫基 丙酸酯,硫水楊酸,氫硫基丁二酸,半胱氨酸及2 -氫 硫基苯駢晖哩。 3. 根據申請專利範園第1項的含鹼性光阻材料汽提組成 物’其中堪原劑的存在量是占汽提姐成物的0.1»:到 1 0重最%。 4. 根據申請專利範圍第3項的含鹼性光阻材料汽提組成 物’其中汽提溶劑包含一或多種溶劑*其選自;過氫 化2-吡咯烷爾,1-甲基2-吡咯烷酮,卜乙基2-吡咯烷 酮* 1-丙基2-吡咯烷酮,1-羥乙基2-吡咯烷酮,1-羥 丙基2-吡咯烷酮、正-環己基吡咯烷酮,具化學式 H〇(CH2CH2-〇-)xR (其中R是具1到4個碳原子的烷基 而X是2或3)之三或二乙二醇單烷基醚,含硫氧化物 的化 0 合物,其選自具化學式ri-Lr2 (其中R1和R2為1至4© I 碳原子的烷基)之二烷基in,二甲亞颯;具化學式 (請先閲讀背面之注意事項再塡寫本頁) 装 *vs 線 R3 本..氏張&度適用㈣國家$準(CNS)A.I死格(210 X 297公梦) 267186 六、申請專利範圍(其中R3是氫•甲基或乙基)之1,1-二氧化四氫噻吩 化合物,四亞甲基砸*甲基四亞甲基δ風和乙基四亞甲 基磾,聚乙二酵,二甲基乙醯胺或二甲基甲醢肢;胺 類是選自親核性胺類* 1-胺基-2-丙酵,卜胺基- 3-丙酵,2-( 2-胺乙氧基)乙醇,2-胺基-乙酵,2-( 2-胺乙胺基)乙醇,2-(2-胺乙胺基)乙胺和卜( 2 -胺乙基六氫吡哄)。 5. 根據申請專利範圍第3項的含鹸性光阻材料汽提姐成 物,其中溶劑包含卜甲基2-吡咯烷嗣,胺包含1-胺基 -2-丙酵或2-胺基乙醇,而堪原劑包含硫水楊酸或抗 壊血酸(維生素C )。 6. —種從含金厲之基片上汽提交聯或硬化光阻材料樹脂 的方法,其改良之處包括使用根據申請專利範圍第1 到5項中任何一項的光阻材料汽提組成物做為該光阻 材料汽提組成物。 ------------装-------1—訂-------「線 (請先閉讀背面之注意事項再塡寫本頁) 經濟部中央5£準局員工消費合作社印纪 本纸唯尺度適用中®國家標準(CNS)A4規格(2丨0 X 29/公坌)
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| US08/133,680 US6326130B1 (en) | 1993-10-07 | 1993-10-07 | Photoresist strippers containing reducing agents to reduce metal corrosion |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW083109330A TW267186B (zh) | 1993-10-07 | 1994-10-07 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US6326130B1 (zh) |
| EP (1) | EP0647884B1 (zh) |
| JP (1) | JP2819392B2 (zh) |
| KR (1) | KR950012144A (zh) |
| CA (1) | CA2132768C (zh) |
| DE (1) | DE69409457T2 (zh) |
| ES (1) | ES2114107T3 (zh) |
| IL (1) | IL111130A0 (zh) |
| TW (1) | TW267186B (zh) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105659167A (zh) * | 2013-10-18 | 2016-06-08 | 松下知识产权经营株式会社 | 抗蚀剂剥离液 |
| TWI691810B (zh) * | 2015-03-13 | 2020-04-21 | 日商長瀨化成股份有限公司 | 光阻劑剝離液 |
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-
1994
- 1994-09-23 CA CA002132768A patent/CA2132768C/en not_active Expired - Fee Related
- 1994-10-03 IL IL11113094A patent/IL111130A0/xx not_active IP Right Cessation
- 1994-10-06 ES ES94115783T patent/ES2114107T3/es not_active Expired - Lifetime
- 1994-10-06 DE DE69409457T patent/DE69409457T2/de not_active Expired - Lifetime
- 1994-10-06 EP EP94115783A patent/EP0647884B1/en not_active Expired - Lifetime
- 1994-10-06 KR KR1019940025492A patent/KR950012144A/ko not_active Ceased
- 1994-10-07 TW TW083109330A patent/TW267186B/zh not_active IP Right Cessation
- 1994-10-07 JP JP6268033A patent/JP2819392B2/ja not_active Expired - Lifetime
-
2001
- 2001-10-02 US US09/968,665 patent/US6749998B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105659167A (zh) * | 2013-10-18 | 2016-06-08 | 松下知识产权经营株式会社 | 抗蚀剂剥离液 |
| TWI691810B (zh) * | 2015-03-13 | 2020-04-21 | 日商長瀨化成股份有限公司 | 光阻劑剝離液 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR950012144A (ko) | 1995-05-16 |
| EP0647884B1 (en) | 1998-04-08 |
| CA2132768C (en) | 2000-09-19 |
| IL111130A0 (en) | 1994-12-29 |
| EP0647884A1 (en) | 1995-04-12 |
| JPH07219241A (ja) | 1995-08-18 |
| DE69409457D1 (de) | 1998-05-14 |
| US20020037479A1 (en) | 2002-03-28 |
| DE69409457T2 (de) | 1998-11-26 |
| CA2132768A1 (en) | 1995-04-08 |
| JP2819392B2 (ja) | 1998-10-30 |
| ES2114107T3 (es) | 1998-05-16 |
| US6326130B1 (en) | 2001-12-04 |
| US6749998B2 (en) | 2004-06-15 |
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