JP7507155B2 - フッ素化アミンオキシド界面活性剤 - Google Patents
フッ素化アミンオキシド界面活性剤 Download PDFInfo
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- JP7507155B2 JP7507155B2 JP2021533423A JP2021533423A JP7507155B2 JP 7507155 B2 JP7507155 B2 JP 7507155B2 JP 2021533423 A JP2021533423 A JP 2021533423A JP 2021533423 A JP2021533423 A JP 2021533423A JP 7507155 B2 JP7507155 B2 JP 7507155B2
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- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 8
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- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 8
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- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
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- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 6
- RFLWCZXTCAXOQE-UHFFFAOYSA-N CN1CCN(CC1)S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F Chemical compound CN1CCN(CC1)S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F RFLWCZXTCAXOQE-UHFFFAOYSA-N 0.000 description 5
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- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
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- 238000010998 test method Methods 0.000 description 5
- YQKDBWLHJXWCOX-UHFFFAOYSA-N 1-(1,1,2,2,3,3,4,4,4-nonafluorobutylsulfonyl)piperazine Chemical compound FC(C(C(C(F)(F)F)(F)F)(F)F)(S(=O)(=O)N1CCNCC1)F YQKDBWLHJXWCOX-UHFFFAOYSA-N 0.000 description 4
- QKSJDOOUAJHQRY-UHFFFAOYSA-N 2-bromoethoxy(trimethyl)silane Chemical compound C[Si](C)(C)OCCBr QKSJDOOUAJHQRY-UHFFFAOYSA-N 0.000 description 4
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 4
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- 229910001218 Gallium arsenide Inorganic materials 0.000 description 4
- IGWUGHRDQMRQNT-UHFFFAOYSA-N N-[3-(diethylamino)propyl]-N-ethyl-1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonamide Chemical compound C(C(F)(F)F)(F)(F)C(C(F)(F)S(=O)(=O)N(CCCN(CC)CC)CC)(F)F IGWUGHRDQMRQNT-UHFFFAOYSA-N 0.000 description 4
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
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- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 3
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- TUJPQFURUYEVFO-UHFFFAOYSA-N N-[2-(diethylamino)ethyl]-1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamide Chemical compound N(C)(S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)CCN(CC)CC TUJPQFURUYEVFO-UHFFFAOYSA-N 0.000 description 3
- BEKXHFLVJGOXRL-UHFFFAOYSA-N N-[3-(diethylamino)propyl]-1,1,2,2,3,3,4,4,4-nonafluoro-N-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]butane-1-sulfonamide Chemical compound FC(C(C(F)(F)F)(F)F)(C(F)(F)S(=O)(=O)N(CCCN(CC)CC)CCOCCOCCOC)F BEKXHFLVJGOXRL-UHFFFAOYSA-N 0.000 description 3
- BFYWGNYLRGXKJZ-UHFFFAOYSA-N N-[3-(dimethylamino)-2,2-dimethylpropyl]-1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamide Chemical compound CC(C)(CN(C)C)CN(C)S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F BFYWGNYLRGXKJZ-UHFFFAOYSA-N 0.000 description 3
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- 238000009616 inductively coupled plasma Methods 0.000 description 3
- 229910000000 metal hydroxide Inorganic materials 0.000 description 3
- 150000004692 metal hydroxides Chemical class 0.000 description 3
- XMRMVBVJGSKMEN-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]-1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonamide Chemical compound CN(C)CCCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F XMRMVBVJGSKMEN-UHFFFAOYSA-N 0.000 description 3
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- WGYKZJWCGVVSQN-UHFFFAOYSA-O propan-1-aminium Chemical compound CCC[NH3+] WGYKZJWCGVVSQN-UHFFFAOYSA-O 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
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- CAZHFGTYGACKSG-UHFFFAOYSA-M 1,1-dimethyl-4-(1,1,2,2,3,3,4,4,4-nonafluorobutylsulfonyl)piperazin-1-ium iodide Chemical compound C[N+]1(CCN(CC1)S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)C.[I-] CAZHFGTYGACKSG-UHFFFAOYSA-M 0.000 description 2
- AKKSSUVDAMMJCL-UHFFFAOYSA-M 1-[1-methyl-4-(1,1,2,2,3,3,4,4,4-nonafluorobutylsulfonyl)piperazin-1-ium-1-yl]octan-1-one iodide Chemical compound CCCCCCCC(=O)[N+]1(CCN(CC1)S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)C.[I-] AKKSSUVDAMMJCL-UHFFFAOYSA-M 0.000 description 2
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- YTYDKDMTKRTNAO-UHFFFAOYSA-M 1-ethyl-4-(1,1,2,2,3,3,4,4,4-nonafluorobutylsulfonyl)-1-propylpiperazin-1-ium iodide Chemical compound CCC[N+]1(CCN(CC1)S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)CC.[I-] YTYDKDMTKRTNAO-UHFFFAOYSA-M 0.000 description 2
- XFHRRYJBHRZPKL-UHFFFAOYSA-M 1-methyl-4-(1,1,2,2,3,3,4,4,4-nonafluorobutylsulfonyl)-1-propylpiperazin-1-ium iodide Chemical compound CCC[N+]1(CCN(CC1)S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)C.[I-] XFHRRYJBHRZPKL-UHFFFAOYSA-M 0.000 description 2
- IUDNRKGPFWUYIC-UHFFFAOYSA-N 2-[2-(2-methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate Chemical compound COCCOCCOCCOS(=O)(=O)C1=CC=C(C)C=C1 IUDNRKGPFWUYIC-UHFFFAOYSA-N 0.000 description 2
- JZVOVVQAVURUJH-UHFFFAOYSA-M 4-(1,1,2,2,3,3,4,4,4-nonafluorobutylsulfonyl)-1,1-dipropylpiperazin-1-ium iodide Chemical compound CCC[N+]1(CCN(CC1)S(=O)(=O)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)CCC.[I-] JZVOVVQAVURUJH-UHFFFAOYSA-M 0.000 description 2
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
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- AMPYMRIIZCRKLS-UHFFFAOYSA-N N-[3-(dimethylamino)-2,2-dimethylpropyl]-1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonamide Chemical compound C(F)(C(C(F)(F)F)(F)F)(C(F)(S(=O)(=O)NCC(C)(CN(C)C)C)F)F AMPYMRIIZCRKLS-UHFFFAOYSA-N 0.000 description 2
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- 230000002378 acidificating effect Effects 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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- 230000007547 defect Effects 0.000 description 2
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- 238000001035 drying Methods 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
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- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 2
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- VUQUOGPMUUJORT-UHFFFAOYSA-N methyl 4-methylbenzenesulfonate Chemical compound COS(=O)(=O)C1=CC=C(C)C=C1 VUQUOGPMUUJORT-UHFFFAOYSA-N 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
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- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 2
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- UDGSVBYJWHOHNN-UHFFFAOYSA-N n',n'-diethylethane-1,2-diamine Chemical compound CCN(CC)CCN UDGSVBYJWHOHNN-UHFFFAOYSA-N 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- VMGZWUXGXSSMAB-UHFFFAOYSA-N n',n'-dimethylpropane-1,3-diamine;hydrofluoride Chemical compound F.CN(C)CCCN VMGZWUXGXSSMAB-UHFFFAOYSA-N 0.000 description 1
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- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000005003 perfluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 125000005005 perfluorohexyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
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- 229920000573 polyethylene Polymers 0.000 description 1
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- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
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- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 241000894007 species Species 0.000 description 1
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- 239000006188 syrup Substances 0.000 description 1
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical class CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/1454—Abrasive powders, suspensions and pastes for polishing
- C09K3/1463—Aqueous liquid suspensions
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/09—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton the carbon skeleton being further substituted by at least two halogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/22—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
- C07D295/26—Sulfur atoms
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09G—POLISHING COMPOSITIONS; SKI WAXES
- C09G1/00—Polishing compositions
- C09G1/02—Polishing compositions containing abrasives or grinding agents
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K13/00—Etching, surface-brightening or pickling compositions
- C09K13/04—Etching, surface-brightening or pickling compositions containing an inorganic acid
- C09K13/08—Etching, surface-brightening or pickling compositions containing an inorganic acid containing a fluorine compound
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- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/004—Surface-active compounds containing F
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0013—Liquid compositions with insoluble particles in suspension
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/042—Acids
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02041—Cleaning
- H01L21/02043—Cleaning before device manufacture, i.e. Begin-Of-Line process
- H01L21/02052—Wet cleaning only
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31105—Etching inorganic layers
- H01L21/31111—Etching inorganic layers by chemical means
-
- 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
- C11D2111/22—Electronic devices, e.g. PCBs or semiconductors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02041—Cleaning
- H01L21/02057—Cleaning during device manufacture
- H01L21/02068—Cleaning during device manufacture during, before or after processing of conductive layers, e.g. polysilicon or amorphous silicon layers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Detergent Compositions (AREA)
- Cleaning Or Drying Semiconductors (AREA)
- Weting (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862778565P | 2018-12-12 | 2018-12-12 | |
| US62/778,565 | 2018-12-12 | ||
| PCT/IB2019/060716 WO2020121248A1 (en) | 2018-12-12 | 2019-12-12 | Fluorinated amine oxide surfactants |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022514222A JP2022514222A (ja) | 2022-02-10 |
| JPWO2020121248A5 JPWO2020121248A5 (enExample) | 2022-12-21 |
| JP7507155B2 true JP7507155B2 (ja) | 2024-06-27 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| JP2021533423A Active JP7507155B2 (ja) | 2018-12-12 | 2019-12-12 | フッ素化アミンオキシド界面活性剤 |
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| US (1) | US20220040655A1 (enExample) |
| JP (1) | JP7507155B2 (enExample) |
| CN (1) | CN113166634A (enExample) |
| TW (1) | TW202035361A (enExample) |
| WO (1) | WO2020121248A1 (enExample) |
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| CN114350366B (zh) * | 2021-12-09 | 2023-04-18 | 湖北兴福电子材料股份有限公司 | 一种氮化硅与p型多晶硅等速蚀刻液 |
| TWI895691B (zh) * | 2023-02-14 | 2025-09-01 | 關東鑫林科技股份有限公司 | 蝕刻液組成物及使用其之蝕刻方法 |
| CN118496473A (zh) * | 2024-05-22 | 2024-08-16 | 智仑新材料科技(西安)有限公司 | 一种低氯环氧树脂的制备方法及一种除氯剂的制备方法 |
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| JP2006505668A (ja) | 2002-11-08 | 2006-02-16 | スリーエム イノベイティブ プロパティズ カンパニー | 水性酸エッチング溶液のためのフッ素化界面活性剤 |
| US20070049646A1 (en) | 2005-08-30 | 2007-03-01 | Moore George G I | Compositions of fluorochemical surfactants |
| JP2007106958A (ja) | 2005-10-17 | 2007-04-26 | Asahi Glass Co Ltd | フッ素系界面活性剤 |
| JP2007526944A (ja) | 2004-03-03 | 2007-09-20 | スリーエム イノベイティブ プロパティズ カンパニー | 水性クリーニング溶液のためのフッ素化スルホンアミド界面活性剤 |
| JP2019519804A (ja) | 2016-06-20 | 2019-07-11 | アーゼッド・エレクトロニック・マテリアルズ(ルクセンブルグ)ソシエテ・ア・レスポンサビリテ・リミテ | リンス組成物、レジストパターンの形成方法および半導体素子の製造方法 |
| JP2020055783A (ja) | 2018-10-03 | 2020-04-09 | 三菱マテリアル電子化成株式会社 | ペルフルオロエーテル含有化合物及びノニオン系含フッ素界面活性剤 |
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| US3772195A (en) * | 1969-06-12 | 1973-11-13 | Minnesota Mining & Mfg | Fire extinguishing composition comprising a fluoroaliphatic surfactant fluorine-free surfactant |
| DK0621057T3 (da) * | 1993-04-23 | 1997-04-28 | Atochem Elf Sa | Emulgatorer til bærbare brandslukkere |
| AU2830997A (en) * | 1996-06-06 | 1998-01-05 | Minnesota Mining And Manufacturing Company | Fire-fighting agents containing adsorbable fluorocarbon surfactants |
| KR20010032921A (ko) * | 1997-12-10 | 2001-04-25 | 스프레이그 로버트 월터 | 흡착성 플루오로카본 계면활성제를 포함하는 소화제 |
| US7160850B2 (en) * | 2004-12-30 | 2007-01-09 | 3M Innovative Properties Company | Compositions of monomeric surfactants |
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- 2019-12-11 TW TW108145329A patent/TW202035361A/zh unknown
- 2019-12-12 CN CN201980080746.9A patent/CN113166634A/zh active Pending
- 2019-12-12 US US17/297,907 patent/US20220040655A1/en not_active Abandoned
- 2019-12-12 JP JP2021533423A patent/JP7507155B2/ja active Active
- 2019-12-12 WO PCT/IB2019/060716 patent/WO2020121248A1/en not_active Ceased
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| US20040089840A1 (en) | 2002-11-08 | 2004-05-13 | 3M Innovative Properties Company | Fluorinated surfactants for buffered acid etch solutions |
| JP2006505668A (ja) | 2002-11-08 | 2006-02-16 | スリーエム イノベイティブ プロパティズ カンパニー | 水性酸エッチング溶液のためのフッ素化界面活性剤 |
| JP2006505667A (ja) | 2002-11-08 | 2006-02-16 | スリーエム イノベイティブ プロパティズ カンパニー | 緩衝酸エッチング溶液のためのフッ素化界面活性剤 |
| JP2007526944A (ja) | 2004-03-03 | 2007-09-20 | スリーエム イノベイティブ プロパティズ カンパニー | 水性クリーニング溶液のためのフッ素化スルホンアミド界面活性剤 |
| US20070049646A1 (en) | 2005-08-30 | 2007-03-01 | Moore George G I | Compositions of fluorochemical surfactants |
| JP2007106958A (ja) | 2005-10-17 | 2007-04-26 | Asahi Glass Co Ltd | フッ素系界面活性剤 |
| JP2019519804A (ja) | 2016-06-20 | 2019-07-11 | アーゼッド・エレクトロニック・マテリアルズ(ルクセンブルグ)ソシエテ・ア・レスポンサビリテ・リミテ | リンス組成物、レジストパターンの形成方法および半導体素子の製造方法 |
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Also Published As
| Publication number | Publication date |
|---|---|
| CN113166634A (zh) | 2021-07-23 |
| JP2022514222A (ja) | 2022-02-10 |
| TW202035361A (zh) | 2020-10-01 |
| WO2020121248A1 (en) | 2020-06-18 |
| US20220040655A1 (en) | 2022-02-10 |
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