JP2009185287A - 固体表面上のイオン液体の濡れ性を改善するための機能添加剤 - Google Patents
固体表面上のイオン液体の濡れ性を改善するための機能添加剤 Download PDFInfo
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- JP2009185287A JP2009185287A JP2009023271A JP2009023271A JP2009185287A JP 2009185287 A JP2009185287 A JP 2009185287A JP 2009023271 A JP2009023271 A JP 2009023271A JP 2009023271 A JP2009023271 A JP 2009023271A JP 2009185287 A JP2009185287 A JP 2009185287A
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- methyl
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- ethyl
- butyl
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- 239000000203 mixture Substances 0.000 claims abstract description 62
- 239000002904 solvent Substances 0.000 claims abstract description 15
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 59
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 39
- 125000000217 alkyl group Chemical group 0.000 claims description 22
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- 125000003118 aryl group Chemical group 0.000 claims description 16
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- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 9
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- 238000000034 method Methods 0.000 claims description 5
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 58
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 30
- 229910052757 nitrogen Inorganic materials 0.000 description 28
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
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- 150000003839 salts Chemical class 0.000 description 8
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- 229910004283 SiO 4 Inorganic materials 0.000 description 7
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 7
- 125000002877 alkyl aryl group Chemical group 0.000 description 7
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 7
- 125000005313 fatty acid group Chemical group 0.000 description 7
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- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical class C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 7
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- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
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- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- 125000000623 heterocyclic group Chemical group 0.000 description 5
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- 125000004433 nitrogen atom Chemical group N* 0.000 description 5
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- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 5
- AMKUSFIBHAUBIJ-UHFFFAOYSA-N 1-hexylpyridin-1-ium Chemical compound CCCCCC[N+]1=CC=CC=C1 AMKUSFIBHAUBIJ-UHFFFAOYSA-N 0.000 description 4
- XDEQOBPALZZTCA-UHFFFAOYSA-N 1-octylpyridin-1-ium Chemical compound CCCCCCCC[N+]1=CC=CC=C1 XDEQOBPALZZTCA-UHFFFAOYSA-N 0.000 description 4
- RGICCULPCWNRAB-UHFFFAOYSA-N 2-[2-(2-hexoxyethoxy)ethoxy]ethanol Chemical compound CCCCCCOCCOCCOCCO RGICCULPCWNRAB-UHFFFAOYSA-N 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 4
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 4
- 229910002651 NO3 Inorganic materials 0.000 description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 4
- 150000008051 alkyl sulfates Chemical class 0.000 description 4
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- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
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- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 4
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 description 3
- ZXMGHDIOOHOAAE-UHFFFAOYSA-N 1,1,1-trifluoro-n-(trifluoromethylsulfonyl)methanesulfonamide Chemical compound FC(F)(F)S(=O)(=O)NS(=O)(=O)C(F)(F)F ZXMGHDIOOHOAAE-UHFFFAOYSA-N 0.000 description 3
- NJMWOUFKYKNWDW-UHFFFAOYSA-N 1-ethyl-3-methylimidazolium Chemical compound CCN1C=C[N+](C)=C1 NJMWOUFKYKNWDW-UHFFFAOYSA-N 0.000 description 3
- PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 3
- QTJISTOHDJAKOQ-UHFFFAOYSA-N 2-hydroxyethylazanium;methyl sulfate Chemical compound [NH3+]CCO.COS([O-])(=O)=O QTJISTOHDJAKOQ-UHFFFAOYSA-N 0.000 description 3
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 3
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- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 description 3
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- FIVJMCNNMIGYRO-UHFFFAOYSA-N bis(2-hydroxyethyl)-dimethylazanium Chemical compound OCC[N+](C)(C)CCO FIVJMCNNMIGYRO-UHFFFAOYSA-N 0.000 description 3
- 150000001642 boronic acid derivatives Chemical class 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 150000003857 carboxamides Chemical class 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
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- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
- ISNICOKBNZOJQG-UHFFFAOYSA-O guanidinium ion Chemical compound C[NH+]=C(N(C)C)N(C)C ISNICOKBNZOJQG-UHFFFAOYSA-O 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 3
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- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 description 2
- YFSUTJLHUFNCNZ-UHFFFAOYSA-M 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YFSUTJLHUFNCNZ-UHFFFAOYSA-M 0.000 description 2
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- CDIWYWUGTVLWJM-UHFFFAOYSA-N 1,3,4-trimethylimidazol-1-ium Chemical compound CC1=C[N+](C)=CN1C CDIWYWUGTVLWJM-UHFFFAOYSA-N 0.000 description 2
- HVVRUQBMAZRKPJ-UHFFFAOYSA-N 1,3-dimethylimidazolium Chemical compound CN1C=C[N+](C)=C1 HVVRUQBMAZRKPJ-UHFFFAOYSA-N 0.000 description 2
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- XUAXVBUVQVRIIQ-UHFFFAOYSA-N 1-butyl-2,3-dimethylimidazol-3-ium Chemical compound CCCCN1C=C[N+](C)=C1C XUAXVBUVQVRIIQ-UHFFFAOYSA-N 0.000 description 2
- GYZXRPOUUZKBAT-UHFFFAOYSA-N 1-butyl-2-ethylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC=C1CC GYZXRPOUUZKBAT-UHFFFAOYSA-N 0.000 description 2
- BHIGPVGNEXDQBL-UHFFFAOYSA-N 1-butyl-2-methylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC=C1C BHIGPVGNEXDQBL-UHFFFAOYSA-N 0.000 description 2
- VZGDWXRMRQTAPB-UHFFFAOYSA-N 1-butyl-3-ethyl-2-methylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC(CC)=C1C VZGDWXRMRQTAPB-UHFFFAOYSA-N 0.000 description 2
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 description 2
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- MKMZBNMOMCOCOA-UHFFFAOYSA-N 1-dodecyl-3-ethyl-2-methylpyridin-1-ium Chemical compound CCCCCCCCCCCC[N+]1=CC=CC(CC)=C1C MKMZBNMOMCOCOA-UHFFFAOYSA-N 0.000 description 2
- ILQHIGIKULUQFQ-UHFFFAOYSA-N 1-dodecyl-3-methylimidazolium Chemical compound CCCCCCCCCCCCN1C=C[N+](C)=C1 ILQHIGIKULUQFQ-UHFFFAOYSA-N 0.000 description 2
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- IRGDPGYNHSIIJJ-UHFFFAOYSA-N 1-ethyl-2,3-dimethylimidazol-3-ium Chemical compound CCN1C=C[N+](C)=C1C IRGDPGYNHSIIJJ-UHFFFAOYSA-N 0.000 description 2
- LNCAFWKXQYNUFX-UHFFFAOYSA-N 1-ethyl-3,4,5-trimethylimidazol-3-ium Chemical compound CCN1C=[N+](C)C(C)=C1C LNCAFWKXQYNUFX-UHFFFAOYSA-N 0.000 description 2
- OIDIRWZVUWCCCO-UHFFFAOYSA-N 1-ethylpyridin-1-ium Chemical compound CC[N+]1=CC=CC=C1 OIDIRWZVUWCCCO-UHFFFAOYSA-N 0.000 description 2
- OPVAFCQZNIZLRH-UHFFFAOYSA-N 1-hexadecyl-2-methylpyridin-1-ium Chemical compound CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1C OPVAFCQZNIZLRH-UHFFFAOYSA-N 0.000 description 2
- SWWLEHMBKPSRSI-UHFFFAOYSA-N 1-hexyl-2,3-dimethylimidazol-3-ium Chemical compound CCCCCCN1C=C[N+](C)=C1C SWWLEHMBKPSRSI-UHFFFAOYSA-N 0.000 description 2
- OLRSYSUCJIKFOL-UHFFFAOYSA-N 1-hexyl-2-methylpyridin-1-ium Chemical compound CCCCCC[N+]1=CC=CC=C1C OLRSYSUCJIKFOL-UHFFFAOYSA-N 0.000 description 2
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- BJMBCVIFMXOIIH-UHFFFAOYSA-N 2-ethyl-1-methylpyridin-1-ium Chemical compound CCC1=CC=CC=[N+]1C BJMBCVIFMXOIIH-UHFFFAOYSA-N 0.000 description 2
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- HRDVJODPWYQQCG-UHFFFAOYSA-N 2-ethyl-1-tetradecylpyridin-1-ium Chemical compound CCCCCCCCCCCCCC[N+]1=CC=CC=C1CC HRDVJODPWYQQCG-UHFFFAOYSA-N 0.000 description 2
- MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 description 2
- UAAXLYUGYHRBLE-UHFFFAOYSA-N 2-methyl-1-octylpyridin-1-ium Chemical compound CCCCCCCC[N+]1=CC=CC=C1C UAAXLYUGYHRBLE-UHFFFAOYSA-N 0.000 description 2
- 125000004398 2-methyl-2-butyl group Chemical group CC(C)(CC)* 0.000 description 2
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- 238000005555 metalworking Methods 0.000 description 1
- MDJFFURNGMSLJP-UHFFFAOYSA-M methanesulfonate;1-(3-methylimidazol-3-ium-1-yl)ethanol Chemical compound CS([O-])(=O)=O.CC(O)N1C=C[N+](C)=C1 MDJFFURNGMSLJP-UHFFFAOYSA-M 0.000 description 1
- XHYYGJAYKIYARQ-UHFFFAOYSA-M methanesulfonate;tetrabutylazanium Chemical compound CS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC XHYYGJAYKIYARQ-UHFFFAOYSA-M 0.000 description 1
- DSQCNXSPLHDLED-UHFFFAOYSA-M methanesulfonate;tetrabutylphosphanium Chemical compound CS([O-])(=O)=O.CCCC[P+](CCCC)(CCCC)CCCC DSQCNXSPLHDLED-UHFFFAOYSA-M 0.000 description 1
- 125000005525 methide group Chemical group 0.000 description 1
- FIMHASWLGDDANN-UHFFFAOYSA-M methyl sulfate;tributyl(methyl)azanium Chemical compound COS([O-])(=O)=O.CCCC[N+](C)(CCCC)CCCC FIMHASWLGDDANN-UHFFFAOYSA-M 0.000 description 1
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- 125000001802 myricyl group Chemical group [H]C([*])([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])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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- CGVLVOOFCGWBCS-RGDJUOJXSA-N n-octyl β-d-thioglucopyranoside Chemical compound CCCCCCCCS[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O CGVLVOOFCGWBCS-RGDJUOJXSA-N 0.000 description 1
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
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- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
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- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- CTYRPMDGLDAWRQ-UHFFFAOYSA-N phenyl hydrogen sulfate Chemical compound OS(=O)(=O)OC1=CC=CC=C1 CTYRPMDGLDAWRQ-UHFFFAOYSA-N 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- 125000005538 phosphinite group Chemical group 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
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- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 1
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- 239000000758 substrate Substances 0.000 description 1
- RVKZDIDATLDTNR-UHFFFAOYSA-N sulfanylideneeuropium Chemical compound [Eu]=S RVKZDIDATLDTNR-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 125000005463 sulfonylimide group Chemical group 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
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- 150000005621 tetraalkylammonium salts Chemical class 0.000 description 1
- WGYONVRJGWHMKV-UHFFFAOYSA-M tetrabutylazanium;benzoate Chemical compound [O-]C(=O)C1=CC=CC=C1.CCCC[N+](CCCC)(CCCC)CCCC WGYONVRJGWHMKV-UHFFFAOYSA-M 0.000 description 1
- RKHXQBLJXBGEKF-UHFFFAOYSA-M tetrabutylphosphanium;bromide Chemical compound [Br-].CCCC[P+](CCCC)(CCCC)CCCC RKHXQBLJXBGEKF-UHFFFAOYSA-M 0.000 description 1
- IBWGNZVCJVLSHB-UHFFFAOYSA-M tetrabutylphosphanium;chloride Chemical compound [Cl-].CCCC[P+](CCCC)(CCCC)CCCC IBWGNZVCJVLSHB-UHFFFAOYSA-M 0.000 description 1
- SBOOKGHQWGEWCB-UHFFFAOYSA-M tetraethylazanium;2,2,2-trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F.CC[N+](CC)(CC)CC SBOOKGHQWGEWCB-UHFFFAOYSA-M 0.000 description 1
- PUZYNDBTWXJXKN-UHFFFAOYSA-M tetraethylazanium;trifluoromethanesulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)F.CC[N+](CC)(CC)CC PUZYNDBTWXJXKN-UHFFFAOYSA-M 0.000 description 1
- YQIVQBMEBZGFBY-UHFFFAOYSA-M tetraheptylazanium;bromide Chemical compound [Br-].CCCCCCC[N+](CCCCCCC)(CCCCCCC)CCCCCCC YQIVQBMEBZGFBY-UHFFFAOYSA-M 0.000 description 1
- VMJQVRWCDVLJSI-UHFFFAOYSA-M tetraheptylazanium;chloride Chemical compound [Cl-].CCCCCCC[N+](CCCCCCC)(CCCCCCC)CCCCCCC VMJQVRWCDVLJSI-UHFFFAOYSA-M 0.000 description 1
- SYZCZDCAEVUSPM-UHFFFAOYSA-M tetrahexylazanium;bromide Chemical compound [Br-].CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC SYZCZDCAEVUSPM-UHFFFAOYSA-M 0.000 description 1
- VRKHAMWCGMJAMI-UHFFFAOYSA-M tetrahexylazanium;iodide Chemical compound [I-].CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC VRKHAMWCGMJAMI-UHFFFAOYSA-M 0.000 description 1
- QBVXKDJEZKEASM-UHFFFAOYSA-M tetraoctylammonium bromide Chemical compound [Br-].CCCCCCCC[N+](CCCCCCCC)(CCCCCCCC)CCCCCCCC QBVXKDJEZKEASM-UHFFFAOYSA-M 0.000 description 1
- SNNIPOQLGBPXPS-UHFFFAOYSA-M tetraoctylazanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](CCCCCCCC)(CCCCCCCC)CCCCCCCC SNNIPOQLGBPXPS-UHFFFAOYSA-M 0.000 description 1
- QVBRLOSUBRKEJW-UHFFFAOYSA-M tetraoctylphosphanium;bromide Chemical compound [Br-].CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC QVBRLOSUBRKEJW-UHFFFAOYSA-M 0.000 description 1
- SPALIFXDWQTXKS-UHFFFAOYSA-M tetrapentylazanium;bromide Chemical compound [Br-].CCCCC[N+](CCCCC)(CCCCC)CCCCC SPALIFXDWQTXKS-UHFFFAOYSA-M 0.000 description 1
- JCEZNVYYPIYZPZ-UHFFFAOYSA-M tetrapentylazanium;thiocyanate Chemical compound [S-]C#N.CCCCC[N+](CCCCC)(CCCCC)CCCCC JCEZNVYYPIYZPZ-UHFFFAOYSA-M 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000007944 thiolates Chemical group 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- RYVBINGWVJJDPU-UHFFFAOYSA-M tributyl(hexadecyl)phosphanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC RYVBINGWVJJDPU-UHFFFAOYSA-M 0.000 description 1
- HJHUXWBTVVFLQI-UHFFFAOYSA-N tributyl(methyl)azanium Chemical compound CCCC[N+](C)(CCCC)CCCC HJHUXWBTVVFLQI-UHFFFAOYSA-N 0.000 description 1
- UFMOMJZZKFLOSJ-UHFFFAOYSA-M trifluoromethanesulfonate;1,2,3-trimethylimidazol-1-ium Chemical compound CC=1N(C)C=C[N+]=1C.[O-]S(=O)(=O)C(F)(F)F UFMOMJZZKFLOSJ-UHFFFAOYSA-M 0.000 description 1
- JCQGIZYNVAZYOH-UHFFFAOYSA-M trihexyl(tetradecyl)phosphanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[P+](CCCCCC)(CCCCCC)CCCCCC JCQGIZYNVAZYOH-UHFFFAOYSA-M 0.000 description 1
- 238000005829 trimerization reaction Methods 0.000 description 1
- LAGQNGWYNLUQRI-UHFFFAOYSA-N trioctylmethylammonium bis(trifluoromethylsulfonyl)imide Chemical compound FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC LAGQNGWYNLUQRI-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- 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
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/28—Heterocyclic compounds containing nitrogen in the ring
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
-
- 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
- C11D1/38—Cationic compounds
- C11D1/60—Sulfonium or phosphonium compounds
-
- 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
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- 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
- C11D1/82—Compounds containing silicon
-
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Abstract
【解決手段】少なくとも1種のイオン液体と少なくとも1種の機能添加剤と、適切な場合、溶媒および/またはさらなる助剤もしくは添加剤とを含む組成物、ならびに固体表面の湿潤剤としてのその使用。
【選択図】なし
Description
イオン液体は、固体表面の濡れ性が重要な役割を果たす多数の用途のために使用され、提案されている。このような用途の例は、潤滑油としておよび分離プロセス、特に蒸留分離プロセスにおける使用である。イオン液体は、しばしば不十分な濡れおよび拡散挙動を有し、したがって、卓越した特性プロフィールにもかかわらず、この欠陥のために適さないことがわかっている。
したがって、イオン液体の濡れおよび拡散挙動を効果的に制御して、固体表面を濡らさなければならない用途に広く永続的に使用できるようにすることが本発明の目的である。液体の適当な濡れ性は、この用途における機能を本質的に改善し得る。
0から20重量%、好ましくは0から10重量%、特に好ましくは0から5重量%の溶媒と、
0から20重量%、好ましくは0から10重量%、特に好ましくは0から5重量%の助剤および添加剤と、
0.001から10重量%、好ましくは0.001から5重量%、特に好ましくは0.05から1重量%の1種以上の本発明の機能添加剤とを含み、
ここで、組成物の全ての成分の合計は100重量%である。
[A]n +[Y]n− (I)
(式中、nは、1、2、3もしくは4であり、[A]+は、第4級アンモニウムカチオン、オキソニウムカチオン、スルホニウムカチオンもしくはホスホニウムカチオンであり、[Y]n−は、1価、2価、3価もしくは4価アニオンである);または
一般式(II)の混合塩
[A1]+[A2]+[Y]2− (IIa);
[A1]+[A2]+[A3]+[Y]3− (IIb);もしくは
[A1]+[A2]+[A3]+[A4]+[Y]4− (IIc)、
(式中、[A1]+、[A2]+、[A3]+および[A4]+は、[A]+について記載された群のうちから独立して選択され、[Y]n−は、式(I)について定義されたとおりである);または
一般式(III)の混合塩
[A1]+[A2]+[A3]+[M1]+[Y]4− (IIIa);
[A1]+[A2]+[M1]+[M2]+[Y]4− (IIIb);
[A1]+[M1]+[M2]+[M3]+[Y]4− (IIIc);
[A1]+[A2]+[M1]+[Y]3− (IIId);
[A1]+[M1]+[M2]+[Y]3− (IIIe);
[A1]+[M1]+[Y]2− (IIIf);
[A1]+[A2]+[M4]2+[Y]4− (IIIg);
[A1]+[M1]+[M4]2+[Y]4− (IIIh);
[A1]+[M5]3+[Y]4− (IIIi);または
[A1]+[M4]2+[Y]3− (IIIj)
(式中、[A1]+、[A2]+および[A3]+は、[A]+について記載された群のうちから独立して選択され、[Y]n−は、式(I)について定義されたとおりであり、[M1]+、[M2]+、[M3]+は、1価金属カチオンであり、[M4]2+は、2価金属カチオンであり、[M5]3+は、3価金属カチオンである);
または全ての式(I)から(III)の混合物の塩である。
R1R2R3R4N+ (IV)
R1R2N+=CR3R4 (V)
R1R2R3R4P+ (VI)
R1R2P+=CR3R4 (VII)
R1R2R3S+ (VIII)
の少なくとも1種のカチオンからなり得る
(式中、
R1、R2、R3、R4は、同じであるか異なり、各々、水素、1から30個の炭素原子を有し、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、5から40個の炭素原子を有し、二重結合を含有してもよい脂環式炭化水素基、6から40個の炭素原子を有する芳香族炭化水素基、7から40個の炭素原子を有するアルキルアリール基、2から30個の炭素原子を有し、1個以上のヘテロ原子(酸素、NH、NR`、ここで、R`は、二重結合を含有してもよいC1〜C30−アルキル基、特に−CH3である)によって介入され、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、2から30個の炭素原子を有し、−O−C(O)−、−(O)C−O−、−NH−C(O)−、−(O)C−NH、−(CH3)N−C(O)−、−(O)C−N(CH3)−、−S(O2)−O−、−O−S(O2)−、−S(O2)−NH−、−NH−S(O2)−、−S(O2)−N(CH3)−、−N(CH3)−S(O2)−からなる群から選択される1つ以上の官能基によって介入され、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、1から30個の炭素原子を有し、OH、OR`、NH2、N(H)R`、N(R`)2(ここで、R`は、二重結合を含有してもよいC1〜C30−アルキル基である)によって末端が官能化され、二重結合または式−(R5−O)n−R6のブロックまたはランダム構造を有するポリエステルを含有してもよい直鎖または分枝脂肪族または脂環式炭化水素基であり、
ここで、
R5は、2から4個の炭素原子を有する直鎖または分枝炭化水素基であり、
nは、1から100、好ましくは2から60であり、
R6は、水素、1から30個の炭素原子を有し、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、5から40個の炭素原子を有し、二重結合を含有してもよい脂環式炭化水素基、6から40個の炭素原子を有する芳香族炭化水素基、7から40個の炭素原子を有するアルキルアリール基または−C(O)−R7基であり、ここで、
R7は、1から30個の炭素原子を有し、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、5から40個の炭素原子を有し、二重結合を含有してもよい脂環式炭化水素基、6から40個の炭素原子を有する芳香族炭化水素基、7から40個の炭素原子を有するアルキルアリール基である)。
(IX)R6 4−mN+[((CH2)n−Q−R7]mX−
の物質が好ましい
(式中:各々の基R6は、独立して、1から6個の炭素原子を有するアルキル基またはヒドロキシアルキル基、またはベンジル基、好ましくはメチル基であり;基R7は、各々、互いに独立して、水素、11から22個の炭素原子を有する直鎖または分枝アルキル基、11から22個の炭素原子を有する直鎖または分枝アルケニル基であり、但し、少なくとも1つの基R7は、水素ではなく;
Qは、−O−CO)−、−C(O)O、−NR8−C(O)−、−C(O)−NR8−、−O−C(O)−O、−CHR9−O−C(O)−または−CH(OCOR7)−CH2−O−C(O)−の式の群のうちから独立して選択され、ここで、R8は、水素、メチル、エチル、プロピルまたはブチルであり、R9は、水素またはメチルであり、Qは、好ましくは−O−C(O)−または−NH−C(O)−であり、mは、1から4、好ましくは2または3であり、nは、1から4、好ましくは2であり;Xは、可塑剤に相溶性のアニオン、例えばクロリド、ブロミド、メチルスルフェート、エチルスルフェート、スルフェートまたはナイトレート、好ましくはクロリドまたはメチルスルフェートである)。第4級アンモニウム化合物は、その値が1からmにわたる、水素ではない異なる基R7を有する化合物の混合物を含有してもよい。このような混合物は、好ましくは、水素ではない、平均1.2から2.5個の基R7を有する。水素ではない基R7の割合は、好ましくは1.4から2.0、より好ましくは1.6から1.9である。
(X) R6N+[CH2CHR9OH−][CH2CHR9OC(O)R7]2X−
(XI) R6N+[CH2CHR9OC(O)R7]2X−
(XII) R6N+[CH2CHR9OH−][CH2CH2NHC(O)R7]2X−の化合物である(式中、R6、R7およびXは、式(i)について上記に定義されたとおりであり、但し、R7は水素ではない)。
N,N−ジ(タローイルオキシエチル)−N,N−ジメチルアンモニウムクロリド(N,N-di(tallowyloxyethyl)-N,N-dimethylammonium chroride);
N,N−ジ(カノリルオキシエチル)−N,N−ジメチルアンモニウムクロリド(N,N-di(canolyloxyethyl)-N,N-dimethylammonium chroride);
N,N−ジ(タローイルオキシエチル)−N−メチル,N−(2−ヒドロキシエチル)アンモニウムメチルスルフェート;
N,N−ジ(カノリルオキシエチル)−N−メチル,N−(2−ヒドロキシエチル)アンモニウムメチルスルフェート;
N,N−ジ(タローイルアミドエチル)−N−メチル,N−(2−ヒドロキシエチル)アンモニウムメチルスルフェート;
N,N−ジ(2−タローイルオキシ−2−オキソエチル)−N,N−ジメチルアンモニウムクロリド;
N,N−ジ(2−カノリルオキシ−2−オキソエチル)−N,N−ジメチルアンモニウムクロリド;
N,N−ジ(2−タローイルオキシエチルカルボニルオキシエチル)−N,N−ジメチルアンモニウムクロリド;
N,N−ジ(2−カノリルオキシエチルカルボニルオキシエチル)−N,N−ジメチルアンモニウムクロリド;
N(2−タローイルオキシ−2−エチル)−N−(2−タローイルオキシ−2−オキソエチル)−N,N−ジメチルアンモニウムクロリド;
N(2−カノリルオキシ−2−エチル)−N(2−カノリルオキシ−2−オキソエチル)−N,N−ジメチルアンモニウムクロリド;
N,N,N−トリ(タローイルオキシエチル)−N−メチルアンモニウムクロリド;
N,N,N−トリ(カノリルオキシエチル)−N−メチルアンモニウムクロリド;
1,2−ジタローイルオキシ−3−N,N,N−トリメチルアンモニオプロピルクロリド;および
1,2−ジカノリルオキシ−3−N,N,N−トリメチルアンモニオプロピルクロリドである。
Rは、水素原子、1から30個の炭素原子を有し、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、5から40個の炭素原子を有し、二重結合を含有してもよい脂環式炭化水素基、6から40個の炭素原子を有する芳香族炭化水素基または7から40個の炭素原子を有するアルキルアリール基である。Xは、酸素原子、硫黄原子または置換窒素原子である(X=O、S、NR1)。
(式中、
R8、R9、R10、R11、R12は、同じであるか異なり、各々、水素、1から30個の炭素原子を有し、二重結合を含有してもよい、直鎖または分枝脂肪族炭化水素基、5から40個の炭素原子を有し、二重結合を含有してもよい脂環式炭化水素基、6から40個の炭素原子を有する芳香族炭化水素基、7から40個の炭素原子を有するアルキルアリール基、1から30個の炭素原子を有し、1個以上のヘテロ原子(酸素、NH、NR`、ここで、R`は、二重結合を含有してもよいC1〜C30−アルキル基である)によって介入され、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、1から30個の炭素原子を有し、−O−C(O)−、−(O)C−O−、−NH−C(O)−、−(O)C−NH、−(CH3)N−C(O)−、−(O)C−N(CH3)−、−S(O2)−O−、−O−S(O2)−、−S(O2)−NH−、−NH−S(O2)−、−S(O2)−N(CH3)−、−N(CH3)−S(O2)−からなる群から選択される1種以上の官能基によって介入され、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、1から30個の炭素原子を有し、OH、OR`、NH2、N(H)R`、N(R`)2(ここで、R`は、二重結合を含有してもよいC1〜C30−アルキル基である)で末端が官能化され、二重結合を含有してもよい直鎖または分枝脂肪族または脂環式炭化水素基または式−(R5−O)n−R6に相当するブロックまたはランダム構造を有するポリエーテルであり、
ここで、
R5は、2から4個の炭素原子を含有する炭化水素基であり、
nは、1から100であり、
R6は、水素、1から30個の炭素原子を有し、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、5から40個の炭素原子を有し、二重結合を含有してもよい脂環式炭化水素基、6から40個の炭素原子を有する芳香族炭化水素基、7から40個の炭素原子を有するアルキルアリール基または−C(O)−R7基であり、ここで、
R7は、1から30個の炭素原子を有し、二重結合を含有してもよい直鎖または分枝脂肪族炭化水素基、5から40個の炭素原子を有し、二重結合を含有してもよい脂環式炭化水素基、6から40個の炭素原子を有する芳香族炭化水素基、7から40個の炭素原子を有するアルキルアリール基である)。
(式中、
・基R1からR5の1つは、メチル、エチルもしくは塩素であり、残りの基R1からR5は、各々、水素であり;
・R3は、ジメチルアミノであり、残りの基R1、R2、R4およびR5は、各々、水素であり;
・全てのR1からR5は、水素であり;
・R2は、カルボキシもしくはカルボキサミドであり、残りの基R1、R2、R4およびR5は、各々、水素であり;または
・R1およびR2もしくはR2およびR3は、1,4−ブタ−1,3−ジエニレンであり、残りの基R1、R2、R4およびR5は、各々、水素である
イオン液体であり;
特に、
・R1からR5は、各々、水素であり;または
・基R1からR5の1つは、メチルもしくはエチルであり、残りの基R1からR5は、各々、水素である)。
(式中、
・R1からR4は、各々、水素であり;または
・基R1からR4の1つは、メチルもしくはエチルであり、残りの基R1からR4は、各々、水素である)。
(式中、
・R1は、水素、メチルもしくはエチルであり、R2からR4は、各々、互いに独立して、水素またはメチルであり;または
・R1は、水素、メチルもしくはエチルであり、R2およびR4は、各々、メチルであり、R3は、水素である)。
(式中、
・R1は、水素、メチルもしくはエチルであり、R2からR4は、各々、互いに独立して、水素もしくはメチルであり;
・R1は、水素、メチルもしくはエチルであり、R2およびR4は、メチルであり、R3は、水素であり;
・R1からR4は、それぞれメチルであり;または
・R1からR4は、それぞれメチルもしくは水素である)。
(式中、
・R1は、水素、メチルまたはエチルであり、R2からR4は、各々、互いに独立して、水素またはメチルである)。
(式中、
・R1は、水素、メチル、エチルまたはフェニルであり、R2からR6は、各々、互いに独立して、水素またはメチルである)。
(式中、
・R1およびR2は、各々、互いに独立して、水素、メチル、エチルまたはフェニルであり、R3からR6は、各々、互いに独立して、水素またはメチルである)。
(式中、
・Rは、Hまたはメチルであり、R1およびR2は、各々、互いに独立して、水素、メチルまたはエチルまたは14から22個、好ましくは16から18個の炭素原子を有する直鎖飽和または不飽和アシル基であり、R3からR6は、各々、互いに独立して、水素、1〜4個の炭素原子を有し、OH基を含有してもよい直鎖飽和アルキル基、好ましくはメチル、または脂肪酸基であり;非常に特に好ましくは、R1およびR2が、脂肪酸基であり、RまたはR2およびR3が脂肪酸基である)。式(XVIIm)に相当するこれらの物質は、特に重要である。文献中、これらには時々、紛らわしい式(式XVIIm’またはXVIIlに類似している)も与えられる。
(式中、
・Rは、Hまたはメチルであり、R1およびR2は、各々、互いに独立して、水素、メチルまたはエチルまたは14から22個、好ましくは16から18個の炭素原子を有する直鎖飽和または不飽和アシル基であり、R3からR6は、各々、互いに独立して、水素、1〜4個の炭素原子を有し、OH基を含有してもよい直鎖飽和アルキル基、好ましくはメチル、または脂肪酸基であり;非常に特に好ましくは、R1およびR2が、脂肪酸基であり、RまたはR2およびR3が脂肪酸基である)。式(XIIIm)に相当するこれらの物質は、特に重要である。文献中、これらには時々、紛らわしい式(式XIIIm’またはXIIIlに類似している)も与えられる。
(式中、
・R1からR3は、各々、互いに独立して、水素、メチルまたはエチルであり、R4からR6は、各々、互いに独立して、水素またはメチルである)。
(式中、
・R1は、水素、メチル、エチルまたはフェニルであり、R2およびR3は、各々、互いに独立して、水素またはメチルである)。
(式中、
・R1およびR2は、各々、互いに独立して、水素、メチル、エチルまたはフェニルであり、R3は、水素、メチルまたはフェニルである)。
(ここで、R1は、水素、メチルもしくはエチルであり、R2およびR3は、各々、互いに独立して、水素もしくはメチルであり、またはR2およびR3は、ともに、1,4−β−1−3−ジエニレンである)。
(式中、
・R1は、水素、メチル、エチルまたはフェニルであり、R2からR9は、各々、互いに独立して、水素もしくはメチルである)。
(式中、
・R1およびR4は、各々、互いに独立して、水素、メチル、エチルまたはフェニルであり、R2およびR3および同様にR5からR8は、各々、互いに独立して、水素またはメチルである)。
(式中、
・R1からR3は、各々、互いに独立して、C1〜C18−アルキルであり;または
・R1からR3は、各々、互いに独立して、水素もしくはC1〜C18−アルキルであり、R4は、2−ヒドロキシエチルであり;または
・R1およびR2は、ともに、1,5−ペンチレンもしくは3−オキサ−1,5−ペンチレンであり、R3は、C1〜C18−アルキル、2−ヒドロキシエチルもしくは2−シアノエチルである)。
(式中、
・R1からR5は、各々、メチルであり;
・R1からR5は、各々、互いに独立して、C1〜C18−アルキルであり;または
・R1からR5は、各々、互いに独立して、水素もしくはC1〜C18−アルキルもしくは2−ヒドロキシエチルである)。
(式中、
・R1およびR2は、各々、互いに独立して、メチル、エチル、1−ブチルもしくは1−オクチルであり、R3は、水素、メチル、エチル、アセチル、−SO2OHもしくは−PO(OH)2であり;
・R1は、メチル、エチル、1−ブチルもしくは1−オクチルであり、R2は、−CH2−CH2−OR4基であり、R3およびR4は、各々、互いに独立して、水素、メチル、エチル、アセチル、−SO2OHもしくは−PO(OH)2であり;または
・R1は、−CH2−CH2−OR4基であり、R2は、−CH2−CH2−OR5基であり、R3からR5は、各々、互いに独立して、水素、メチル、エチル、アセチル、−SO2OHもしくは−PO(OH)2であり;
・R1は、メチル、エチル、1−ブチル、1−オクチル、アセチル、−SO2OHもしくは−PO(OH)2であり、R3からR5は、各々、互いに独立して、水素、メチル、エチル、アセチル、−SO2OH、−PO(OH)2もしくは−(CnH2nO)mR1であり、ここで、n=1から5であり、m=1から100である)。
・R1からR3は、各々、互いに独立して、C1〜C18−アルキル、特にブチル、イソブチル、1−ヘキシルまたは1−オクチルである。
・式:F−、Cl−、Br−、I−、BF4 −、PF6 −、AlCl4 −、Al2Cl7 −、Al3Cl10 −、AlBr4 −、FeCl4 −、BCl4 −、SbF6 −、AsF6 −、ZnCl3 −、SnCl3 −、CuCl2 −、CF3SO3 −、(CF3SO3)2N−、CF3CO2 −、CCl3CO2 −、CN−、SCN−、OCN−、NO2 −、NO3 −、N(CN)−のハロゲン化物およびハロゲン含有化合物の群;
・一般式:SO4 2−、HSO4 −、SO3 2”、HSO3 −、RaOSO3 −、RaSO3 −のスルフェート、サルファイトおよびスルホネートの群;
・一般式:PO4 3−、HPO4 2、H2PO4−、RaPO4 2−、HRaPO4 −、RaRbPO4 −のホスフェートの群;
・一般式:RaHPO3 −、RaRbPO2 −、RaRbPO3 −のホスホネートおよびホスフィネートの群;
・一般式:PO3 3−、HPO3 2−、H2PO3 −、RaPO3 2−、RaHPO3 −、RaRbPO3 −のホスファイトの群;
・一般式:RaRbPO2 −、RaHPO2 −、RaRbPO−、RaHPO−のホスホナイトおよびホスフィナイトの群;
・一般式:RaCOO−のカルボキシレートの群;
・一般式:BO3 3−、HBO3 2−、H2BO3 −、RaRbBO3 −、RaHBO3 −、RaBO3 2−、B(ORa)(ORb)(ORc)(ORd)−、B(HSO4)−、B(RaSO4)−のボレートの群;
・一般式:RaBO2 2−、RaRbBO−のボロネートの群;
・一般式:HCO3 −、CO3 2−、RaCO3 −のカーボネートおよびカーボネートエステルの群;
・一般式:SiO4 4−、HSiO4 3−、H2SiO4 2−、H3SiO4 −、RaSiO4 3−、RaRbSiO4 2−、RaRbRcSiO4 −、HRaSiO4 2−、H2RaSiO4 −、HRaRbsiO4 −のシリケートおよびシリケートエステルの群;
・一般式:RaSiO3 3−、RaRbSiO2 2−、RaRbRcSiO−、RaRbRcSiO3 −、RaRbRcSiO2 −、RaRbSiO3 2−のアルキルシランおよびアリールシラン塩の群;
・一般式:
・一般式:
・一般式:RaO−のアルコキシドおよびアリールオキシドの群;
・一般式[MrHalt]s−(ここで、Mは、金属であり、Halは、フッ素、塩素、臭素またはヨウ素であり、rおよびtは、正の整数であり、この錯体の化学量論を示し、sは、正の整数であり、この錯体上の電荷を示す)のハロメタレートの群;
・一般式:S2−、HS−、[Sv]2−、[HSv]−、[RaS]−(ここで、vは、2から10までの正の整数である)の硫化物、硫化水素、多硫化物、多硫化水素およびチオレートの群;
・Fe(CN)6 3−、Fe(CN)6 4−、MnO4 −、Fe(CO)4 −などの金属錯イオンの群
から選択される。
・水素;
・C1〜C30−アルキルおよびそれらのアリール−、ヘテロアリール−、シクロアルキル、ハロゲン−、ヒドロキシ−、アミノ−、カルボキシ−、ホルミル−、−O−、−CO−、−CO−O−または−CO−N<で置換された成分、例えば、メチル、エチル、1−プロピル、2−プロピル、1−ブチル、2−ブチル、2−メチル−1−プロピル(イソブチル)、2−メチル−2−プロピル(tert−ブチル)、1−ペンチル、2−ペンチル、3−ペンチル、2−メチル−1−ブチル、3−メチル−1−ブチル、2−メチル−2−ブチル、3−メチル−2−ブチル、2,2−ジメチル−1−プロピル、1−ヘキシル、2−ヘキシル、3−ヘキシル、2−メチル−1−ペンチル、3−メチル−1−ペンチル、4−メチル−1−ペンチル、2−メチル−2−ペンチル、3−メチル−2−ペンチル、4−メチル−2−ペンチル、2−メチル−3−ペンチル、3−メチル−3−ペンチル、2,2−ジメチル−1−ブチル、2,3−ジメチル−1−ブチル、3,3−ジメチル−1−ブチル、2−エチル−1−ブチル、2,3−ジメチル−2−ブチル、3,3−ジメチル−2−ブチル、ヘプチル、オクチル、ノニル、デシル、ウンデシル、ドデシル、トリデシル、テトラデシル、ペンタデシル、ヘキサデシル、ヘプタデシル、オクタデシル、ノナデシル、イコシル、ヘンイコシル、ドコシル、トリコシル、テトラコシル、ペンタコシル、ヘキサコシル、ヘプタコシル、オクタコシル、ノナコシル、トリアコンチル、フェニルメチル(ベンジル)、ジフェニルメチル、トリフェニルメチル、2−フェニルエチル、3−フェニルプロピル、シクロペンチルメチル、2−シクロペンチルエチル、3−シクロペンチル−プロピル、シクロヘキシルメチル、2−シクロヘキシルエチル、3−シクロヘキシルプロピル、メトキシ、エトキシ、ホルミル、アセチルまたはCqF2(q−a)+(1−b)H2a+b(ここで、q<30であり、0≦a≦qであり、b=0または1である)(例えば、CF3、C2F5、CH2CH2−C(q−2)F2(q−2)+1、C6F13、C8F17、C10F21、C12E25);
・C3〜C12−シクロアルキルおよびそのアリール−、ヘテロアリール−、シクロアルキル−、ハロゲン−、ヒドロキシ−、アミノ−、カルボキシ−、ホルミル−、−O−、−CO−または−CO−O−で置換された成分、例えば、シクロペンチル、2−メチル−1−シクロペンチル、3−メチル−1−シクロペンチル、シクロヘキシル、2−メチル−1−シクロヘキシル、3−メチル−1−シクロヘキシル、4−メチル−1−シクロヘキシルまたはCqF2(q−a)−(1−b)H2a−b(ここで、q≦30であり、0≦a≦qであり、b=0または1である);
・C2〜C30−アルケニルおよびそのアリール−、ヘテロアリール−、シクロアルキル−、ハロゲン−、ヒドロキシ−、アミノ−、カルボキシ−、ホルミル−、−O−、−CO−または−CO−O−で置換された成分、例えば、2−プロペニル、3−ブテニル、シス−2−ブテニル、トランス−2−ブテニルまたはCqF2(q−a)−(1−b)H2a−b(ここで、q≦30であり、0≦a≦qであり、b=0または1である);
・C3〜C12−シクロアルケニルおよびそのアリール−、ヘテロアリール−、シクロアルキル−、ハロゲン−、ヒドロキシ−、アミノ−、カルボキシ−、ホルミル−、−O−、−CO−または−CO−O−で置換された成分、例えば、3−シクロペンテニル、2−シクロヘキセニル、3−シクロヘキセニル、2,5−シクロヘキサジエニルまたはCqF2(q−a)−3(1−b)H2a−3b(ここで、q≦30であり、0≦a≦qであり、b=0または1である);
・2から30個の炭素原子を有するアリールまたはヘテロアリールおよびそのアルキル−、アリール−、ヘテロアリール−、シクロアルキル−、ハロゲン−、ヒドロキシ−、アミノ−、カルボキシ−、ホルミル−、−O−、−CO−または−CO−O−で置換された成分、例えば、フェニル、2−メチルフェニル(2−トリル)、3−メチルフェニル(3−トリル)、4−メチルフェニル、2−エチルフェニル、3−エチルフェニル、4−エチルフェニル、2,3−ジメチルフェニル、2,4−ジメチルフェニル、2,5−ジメチルフェニル、2,6−ジメチルフェニル、3,4−ジメチルフェニル、3,5−ジメチルフェニル、4−フェニルフェニル、1−ナフチル、2−ナフチル、1−ピロリル、2−ピロリル、3−ピロリル、2−ピリジニル、3−ピリジニル、4−ピリジニルまたはC6F(5−a)Ha(ここで、0≦a≦5である)であり;あるいは
・2つの基は、官能基、アリール、アルキル、アリールオキシ、アルキルオキシ、ハロゲン、ヘテロ原子および/または複素環で置換されてよく、1個以上の酸素および/または硫黄原子および/または1個以上の置換または非置換イミノ基によって介入されてもよい不飽和、飽和または芳香族環を形成するものである。
エチル)ジメチル−アンモニウムオキサレート、ビス−(ヒドロキシエチル)ジメチルアンモニウムタルトレートである。
0から20重量%、好ましくは0から10重量%および特に好ましくは0から5重量%の溶媒と、
0から20重量%、好ましくは0から10重量%および特に好ましくは0から5重量%の助剤および添加剤と、
0.001から10重量%、好ましくは0.001から5重量%および特に好ましくは0.05から1重量%の1種以上の本発明の機能添加剤とを含み、
ここで、組成物の全ての成分の合計は、100重量%である。
−(CH2−)g(OC2H4−)h(OC3H6−)i(OC4H8)j(OCH2CH(C6H5))kOR20
である
(ここで、
R20は、水素、アルキルまたはカルボキシル基である。
R20は、好ましくは、水素またはメチル基またはアセチル基である。
指数gは、0から6であり、
指数hは、0から20であり、
指数iは、0から50であり、ここで、h+i≧1であり、
指数jは、0から10であり、
指数kは、0から10である)。
・一般式
・一般式
・一般式
・一般式
・アルキルホスフィンオキシド、例えば、ジメチルデシルホスフィンオキシド(APO 10の商品名で市販されている)
・アルキル−N−グルカミド、例えば、オクチル−N−グルカミド(MEGA-10の商品名で市販されている)
・アルキルグルコシド、例えば、n−ノニル−β−D−グルコピラノシドまたはオクチル−β−D−チオグルコピラノシド(AGNIQUE PGシリーズの商品名で市販されている)
・胆汁酸、例えば、コラン酸またはコール酸
・一般式
R21−P
のアルキルアルコキシレート、例えば、ポリエチレングリコールp−1、1、3、3−テトラメチルブチル)フェニルエーテル(TRITON X-100の商品名で市販されている)、またはポリエチレングリコールイソトリデシルエーテル(GENAPOL X-080もしくはTEGO Alkanol TD 6の商品名で市販されている)、またはポリエチレングリコールステアリルエーテル(TEGO Alkanol S 2、S 10、S 20Pの商品名で市販されている)、またはポリエチレングリコールオレイルエーテル(TEGO Alkanol O 20の商品名で市販されている)、またはポリプロピレングリコールミリスチルエーテル(VARONIC APMの商品名で市販されている)、またはポリエチレングリコールノニルフェニルエーテル(REWOPAL HV 10の商品名で市販されている)、またはポリエチレングリコール−ポリプロピレングリコールコポリマー(PLURONIC、例えば、F68もしくはF127の商品名で市販されている)
・ポリエーテルポリオール(例えば、TERGITOL L-62 EおよびL-62およびL-81の商品名で市販されている)
・一般式
・ソルビタンエステルエトキシレート、例えば、ポリオキシエチレンソルビタンモノラウレート(TEGO SML 20の商品名で市販されている)、またはポリエチレングリコールモノオレエート(TEGO SMOの商品名で市販されている)、またはポリエチレングリコールソルビタントリステアレート(TEGO STSの商品名で市販されている)
・一般式
R21−OH
の脂肪アルコール、例えば、イソステアリルアルコール(TEGO Alkanol 66の商品名で市販されている)、またはオレイルアルコール(TEGO Alkanol 80、85および90の商品名で市販されている)、
・一般式
・一般式
・エステルエトキシレート、例えば、ポリエチレングリコールグリセリルラウレート(TAGAT L2の商品名で市販されている)、またはポリエチレングリコールグリセリルオレオリシノレート(TAGAT V20の商品名で市販されている)、またはポリエチレングリコールグリセリルココエート(Varonic LIの商品名で市販されている)
・有機変性シロキサン(organomodified siloxanes)、例えば:TEGOPRENシリーズまたはTEGO WETシリーズの商品名で市販されているポリエーテルシロキサン。
(式中、
基Rfは、基R1であってよく、ここで、
R1は、1から4個の炭素原子を有するアルキル基もしくはアリール基であり、
または
基Rfは、基R2もしくはR3であり、但し、少なくとも1つの基Rfは、基R2であり、ここで、
R2およびR3は、互いに独立して、式(XIX)
(F)q(O(C2H4−dR’dO)m(CxH2xO)rZ)w (XIX)
のポリエーテル基であり、
ここで、
dは、1から3であり、
mは、>1であり、
qは、0もしくは1であり、
xは、2から10であり、
rは、>1であり、
wは、1から4であり、
Fは、分枝であってもよい炭化水素基であり、
R’は、水素基、1から18個の炭素原子を有する1価炭化水素基であり、
Zは、H原子、またはアルキルもしくはアルキルエステルもしくはアリールエステルなどの1価有機基であり、
ここで、式(XIII)において
bは、0から8であり、
aは、bが、6から8である場合、1から100であり、
aは、bが、3から6である場合、1から200であり、
aは、bが、0から3である場合、1から300である)。
(式中、
m=0から30であり、
k=1から5であり、
R1は、1から10個のエチレンオキシド分子および1から25個のプロピレンオキシド分子と反応させたアリルアルコールまたはアルキル開始ポリエーテル(alkyl-initiated polyether)であり、
・例えば、商品名TEGOPREN 7100の商品名で市販されている官能化ポリエーテルシロキサン
・ブロック構造を有するポリエーテルシロキサン
である。
基Aは、平均式(XXII)
[(C2H4−dR’dO)n(CxH2xO)r(C2H4−dR”dO)t] (XXII)
のポリオキシアルキレンブロックであり、
ここで、
dは、1から3であり、
nは、≧0であり、
xは、2から10であり、
rは、≧0であり、
tは、0であり、
n+r+t≧1であり、
R’は、1価芳香族、置換または非置換炭化水素基であり、
R”は、水素基、または1から18個の炭素原子を有する1価炭化水素基であり、
R1は、H原子、C1〜C40の鎖長を有する1価有機直鎖もしくは分枝アルキル基、または分枝もしくは非分枝アルキルエステルもしくはアリールエステルのカルボキシル基であり、
基Bは、平均式(XXIII)
ここで、
基R2は、同じか異なっており、各々、1から4個の炭素原子を有するアルキル基またはフェニル基であり、
yは、5から200であり、
mは、2から100であり、
pは、0または1であり、
qは、0または1である)、
あるいは、式(XXVI)
(式中、
基R1、基A、基Bおよびm、pおよびqは、上記に定義されたとおりであり、
基Cは、2から20個の炭素原子を有する直鎖または分枝アルキレン基である)。
・テトラアルキルアンモニウム塩、例えば、セチルトリメチルアンモニウムブロミド
・アルキルピリジニウム塩、例えば、セチルピリジニウムクロリド
・一般式
・一般式
・例えば、REWOQUAT W 90、VARIQUAT 55またはREWOQUAT W3690の商品名で市販されている、イミダゾリニウムクアット、
・例えば、VARIQUAT 638(N−メチル−N,N−ビス(2−ヒドロキシエチル)−N−ココアンモニウムクロリド)の商品名で市販されている、アルコキシアルキルクアット、
・一般式
・例えば、TEGOPREN 6921(ジ第4級ポリジメチルシロキサン]、TEGOPREN 6924[ジ第4級ポリジメチルシロキサン)およびTEGOPREN 7990(ジ第4級ポリエーテルポリジメチルシロキサン)の商品名で市販されている、シリコーンクアット。
・一般式
・一般式
・一般式
・一般式
・一般式
・例えば、TEGOPREN 6950の商品名で市販されているシリコーンベタイン。
・パーフルオロアルキルスルホネート、例えば、パーフルオロオクタンスルホネート(PFOS)
・パーフルオロカルボン酸、例えば、パーフルオロオクタン酸(PFOA)
・フッ化テロメアアルコール(fluorinated telomere alcohol)。
・例えば、SURFYNOL 104の商品名で市販されているアセチルジオール
・例えば、SURFYNOL 400またはSURFYNOL 2502の商品名で市販されているアセチレンジオールアルコキシレート
・例えば、DYNOL 604の商品名で市販されているアセチレングリコール
・例えば、ENVIROGEM ADO1、ENVIRONGEM AE01、ENVIRONGEM AE02およびENVIRONGEM AE03の商品名で市販されているアルカンジオール、アルカンジカルボン酸およびそれらのエステル
・ENVIRONGEM 360
・ビスピリジニオアルカン、例えば、1,4−ビス(α−オクチルピリジノ)ブタンジブロミドまたは1,4−ビス(α−ドデシルピリジニウム)ブタンジクロリド
・例えば、TEGO TWIN 4000の商品名で市販されている、EP Al−1 382 632に記載されているシロキサンベースのジェミニ界面活性剤。EP Al−1 382 632の内容は、本開示に参照により全体的に組み込まれている。
TEGO、TEGOSURF、AROSURF、REWOQUAT、VARONIC、ADOGEN、REWOMID、VARAMID、REWOCOROS、REWOPALは、Evonik Goldschmidt GmbHの商標である。
SURFYNOL、DYNOL、ENVIROGEMは、Air Products,Incの商標である。
AGNIQUEは、Cognisの商標である。
TRITONは、DOW Chemical Companyの商標である。
GENAPOLは、Clariantの商標である。
PLURONICは、BASF AGの商標である。
EMPIGENは、Albright&Wilsonの商標である。
VAROXは、R.T.Vanderbiltの商標である。
ZWITTERGENTは、Calbiochem−Novachemの商標である。
8gのイオン液体(IL)を、容器に置き、0.04gの機能添加剤を計量した。このサンプルを、均一になるまでスパチュラで撹拌し、続いて50μlを、PPフィルム上にピペットで移した。5分後の最大拡散を測定した。得られた円の直径(D)を、mm単位で測定する。測定値が高ければ高いほど、拡散および濡れならびにしたがって本発明の機能添加剤の効果が大きい。
イオン液体の濡れ挙動/拡散挙動(5分後に測定された拡散)。濃度は、上記の実験手順によって与えられる。測定は、室温で実施された。
Claims (15)
- 固体表面の永続的な濡れのための組成物であって、少なくとも1種のイオン液体および少なくとも1種の機能添加剤および、適切な場合、溶媒および/またはさらなる助剤もしくは添加剤を含む組成物。
- 湿潤剤または展着剤が、機能添加剤として使用されることを特徴とする、請求項1に記載の組成物。
- 単相からなることを特徴とする、請求項1または2に記載の組成物。
- 1種以上の界面活性剤が、機能添加剤として使用されることを特徴とする、請求項1から3の少なくとも一項に記載の組成物。
- 前記界面活性剤が、非イオン界面活性剤、カチオン界面活性剤、両性界面活性剤およびパーフルオロ界面活性剤からなる群から単独でまたはそれらの混合物としてのいずれかで選択されることを特徴とする、請求項4に記載の組成物。
- 有機溶媒または水および/またはそれらの混合物が、溶媒として使用されることを特徴とする、請求項1から5の少なくとも一項に記載の組成物。
- 前記溶媒が、有機溶媒であることを特徴とする、請求項6に記載の組成物。
- 有機変性シロキサンが、非イオン界面活性剤として使用されることを特徴とする、請求項5に記載の組成物。
- 前記有機変性シロキサンが、ポリエーテルシロキサンであることを特徴とする、請求項8に記載の組成物。
- 一般式(XVIII)
(式中、
基Rfは、基R1であってよく、ここで、
R1は、1から16個の炭素原子を有するアルキル基もしくはアリール基であり、
または
基Rfは、基R2もしくはR3であり、但し、少なくとも1つの基Rfは、基R2であり、ここで、
R2およびR3は、互いに独立して、式(XIX)
(F)q(O(C2H4−dR’dO)m(CxH2xO)rZ)w (XIX)
のポリエーテル基であり、
ここで、
dは、1から3であり、
mは、>1であり、
qは、0もしくは1であり、
xは、2から10であり、
rは、>1であり、
wは、1から4であり、
Fは、分枝であってもよい炭化水素基であり、
R’は、水素基、1から18個の炭素原子を有する1価炭化水素基であり、
Zは、H原子、またはアルキルもしくはアルキルエステルもしくはアリールエステルなどの1価有機基であり、
ここで、式(XVIII)において
bは、0から8であり、
aは、bが6から8である場合、1から100であり、
aは、bが3から6である場合、1から200であり、
aは、bが0から3である場合、1から300である)。 - 前記組成物が、単相からなることを特徴とする、請求項1から10の少なくとも一項に記載の組成物。
- 前記機能添加剤を含まないものと比べて少なくとも10°小さい接触角が達成され得ることを特徴とする、請求項1から11の少なくとも一項に記載の組成物の使用。
- イオン液体により固体表面を濡らす方法における、請求項1から11のいずれか一項に記載の組成物の使用。
- 濡れた面積が、添加剤を含まないものと比べて少なくとも30%大きいことを特徴とする、請求項13に記載の使用。
- 前記表面が、ガラス、金属または合金、セラミック、紙、半導体、ポリマー、石または革からなることを特徴とする、請求項12から14のいずれか一項に記載の使用。
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016113661A (ja) * | 2014-12-15 | 2016-06-23 | Jfeスチール株式会社 | 連続溶融亜鉛めっき方法及び連続溶融亜鉛めっき設備 |
JP2022510675A (ja) * | 2018-12-04 | 2022-01-27 | エボニック オペレーションズ ゲーエムベーハー | 湿潤ガス混合物の除湿方法 |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2088389B1 (de) * | 2008-02-05 | 2017-05-10 | Evonik Degussa GmbH | Absorptionskältemaschine |
EP2087930A1 (de) | 2008-02-05 | 2009-08-12 | Evonik Degussa GmbH | Verfahren zur Absorption eines flüchtigen Stoffes in einem flüssigen Absorptionsmittel |
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EP2398753B1 (de) * | 2009-02-23 | 2017-04-26 | Basf Se | Destillation ionischer flüssigkeiten unter verwendung eines destillationshilfsmittels |
US9428718B2 (en) | 2009-06-30 | 2016-08-30 | Ionfield Holdings, Llc | Liquid mixture to clean dielectric barrier discharge surfaces |
US8741105B2 (en) | 2009-09-01 | 2014-06-03 | Awi Licensing Company | Cellulosic product forming process and wet formed cellulosic product |
DE102009047564A1 (de) | 2009-12-07 | 2011-06-09 | Evonik Degussa Gmbh | Arbeitsmedium für eine Absorptionskältemaschine |
WO2011151785A1 (en) * | 2010-06-01 | 2011-12-08 | Basf Se | Composition for metal electroplating comprising leveling agent |
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CN103313771B (zh) * | 2010-12-30 | 2015-07-15 | 费伊肯私人有限公司 | 采用离子液体脱水的方法 |
US9779879B2 (en) * | 2011-02-25 | 2017-10-03 | Ecole Polytechnique Federale De Lausanne (Epfl) | Redox couple for electrochemical and optoelectronic devices |
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EP2530138A1 (de) * | 2011-06-03 | 2012-12-05 | Carl Bechem Gmbh | Schmierstoff mit verringerter Rückstandsviskosität |
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BR112014008497A2 (pt) | 2011-11-14 | 2017-04-11 | Evonik Degussa Gmbh | método e dispositivo para a separação de gases acídicos a partir de uma mistura de gás |
DE102012200907A1 (de) | 2012-01-23 | 2013-07-25 | Evonik Industries Ag | Verfahren und Absorptionsmedium zur Absorption von CO2 aus einer Gasmischung |
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CN103426655B (zh) * | 2012-05-14 | 2017-06-27 | 海洋王照明科技股份有限公司 | 一种双层电容器用电解液及其制备方法 |
US8481474B1 (en) | 2012-05-15 | 2013-07-09 | Ecolab Usa Inc. | Quaternized alkyl imidazoline ionic liquids used for enhanced food soil removal |
US8716207B2 (en) | 2012-06-05 | 2014-05-06 | Ecolab Usa Inc. | Solidification mechanism incorporating ionic liquids |
EA201590725A1 (ru) * | 2012-11-19 | 2015-11-30 | Массачусетс Инститьют Оф Текнолоджи | Устройство и способы применения пропитанных жидкостью поверхностей |
WO2014084296A1 (ja) * | 2012-11-30 | 2014-06-05 | 日本化薬株式会社 | 色素増感太陽電池 |
WO2016181983A1 (ja) * | 2015-05-12 | 2016-11-17 | 旭硝子株式会社 | 低反射膜付き基体 |
DE102015212749A1 (de) | 2015-07-08 | 2017-01-12 | Evonik Degussa Gmbh | Verfahren zur Entfeuchtung von feuchten Gasgemischen |
AU2016355706B2 (en) * | 2015-11-20 | 2020-02-06 | Hexion Inc. | Chemical products for surface protection |
TWI625232B (zh) * | 2016-02-26 | 2018-06-01 | Fujifilm Corp | 積層體、積層體的製造方法、半導體元件以及半導體元件的製造方法 |
EP3257568B1 (de) | 2016-06-14 | 2019-09-18 | Evonik Degussa GmbH | Verfahren zur entfeuchtung von feuchten gasgemischen mit ionischen flüssigkeiten |
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DE102016210484A1 (de) | 2016-06-14 | 2017-12-14 | Evonik Degussa Gmbh | Verfahren zur Entfeuchtung von feuchten Gasgemischen |
DE102016210483A1 (de) | 2016-06-14 | 2017-12-14 | Evonik Degussa Gmbh | Verfahren und Absorptionsmittel zur Entfeuchtung von feuchten Gasgemischen |
DE102016210481B3 (de) | 2016-06-14 | 2017-06-08 | Evonik Degussa Gmbh | Verfahren zum Reinigen einer ionischen Flüssigkeit |
US10954448B2 (en) | 2017-08-18 | 2021-03-23 | Canadian Natural Resources Limited | High temperature paraffinic froth treatment process |
JP2023522034A (ja) * | 2020-04-16 | 2023-05-26 | トタルエナジーズ・ワンテック | アンモニウム系イオン液体およびそれの潤滑剤用添加剤としての使用 |
CN113880205B (zh) * | 2020-07-02 | 2022-07-12 | 中国石油化工股份有限公司 | 一种木质素基絮凝剂 |
CN114958454B (zh) * | 2022-05-26 | 2023-10-10 | 金宏气体股份有限公司 | 离子液体组合物及其制备方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003186138A (ja) * | 2001-11-21 | 2003-07-03 | Eastman Kodak Co | イオン性液体を含む疎水性有機相の分散体を含んで成る組成物 |
JP2005530910A (ja) * | 2002-06-28 | 2005-10-13 | ザ プロクター アンド ギャンブル カンパニー | イオン性液体系製品及びその使用方法 |
JP2006083211A (ja) * | 2004-09-14 | 2006-03-30 | Shin Etsu Chem Co Ltd | 防汚性縮合硬化型オルガノポリシロキサン組成物及び水中構造物 |
JP2007070370A (ja) * | 2004-09-03 | 2007-03-22 | Kansai Paint Co Ltd | 塗料組成物 |
WO2007144286A1 (en) * | 2006-06-14 | 2007-12-21 | Ciba Holding Inc. | Anti-microbial compositions |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6090758A (en) * | 1997-01-07 | 2000-07-18 | Exxon Research And Engineering Co. | Method for reducing foaming of lubricating oils |
WO2001019507A1 (en) * | 1999-09-17 | 2001-03-22 | Stepan Company | Ternary surfactant blends comprising cationic, anionic, and bridging surfactants and methods of preparing same |
US6403163B1 (en) * | 2000-06-27 | 2002-06-11 | Chemrex, Inc. | Method of treating surfaces with organosilicon water repellent compositions |
DE10232115A1 (de) | 2002-07-16 | 2004-02-05 | Goldschmidt Ag | Organopolysiloxane zur Entschäumung wässriger Systeme |
US7737102B2 (en) * | 2004-11-01 | 2010-06-15 | The Procter & Gamble Company | Ionic liquids derived from functionalized anionic surfactants |
DE102004053167A1 (de) * | 2004-11-01 | 2006-05-04 | Degussa Ag | Polymere Absorptionsmittel für die Gasabsorption und Absorptionsprozess |
US7776810B2 (en) * | 2004-11-01 | 2010-08-17 | The Procter & Gamble Company | Compositions containing ionic liquid actives |
EP1848790B1 (en) * | 2005-02-14 | 2015-04-08 | Advanced Process Technologies, LLC. | Semiconductor cleaning |
DE102005028451B4 (de) * | 2005-06-17 | 2017-02-16 | Evonik Degussa Gmbh | Verfahren zum Transport von Wärme |
DE102005061782A1 (de) * | 2005-12-23 | 2007-06-28 | Goldschmidt Gmbh | Silikonhaltige Pfropfmischpolymere auf Basis styroloxidbasierter Silikonpolyether |
DE102006040122B3 (de) * | 2006-08-26 | 2007-10-31 | Degussa Gmbh | Enteisungsmittel und/oder Vereisungsschutzmittel |
DE102006041088A1 (de) * | 2006-09-01 | 2008-03-06 | Evonik Goldschmidt Gmbh | Siliconhaltige, blockweise aufgebaute Pfropfmischpolymere |
GB0623108D0 (en) * | 2006-11-20 | 2006-12-27 | Sericol Ltd | A printable composition |
EP2087931A3 (de) * | 2008-02-05 | 2011-08-31 | Evonik Goldschmidt GmbH | Entschäumung von ionischen Flüssigkeiten |
US7985719B2 (en) * | 2008-04-28 | 2011-07-26 | Ward Irl E | Cutting and lubricating composition for use with a wire cutting apparatus |
DE102008001674A1 (de) * | 2008-05-09 | 2009-11-12 | Evonik Goldschmidt Gmbh | Flüssige Leitfähigkeitsadditive für nichtwässrige Hydrauliköle |
DE102008040486A1 (de) * | 2008-07-17 | 2010-01-21 | Evonik Goldschmidt Gmbh | Verwendung von ionischen Flüssigkeiten als Zusatzstoff für Reinigungsverfahren in verflüssigtem und/oder überkritischem Gas |
-
2009
- 2009-01-30 EP EP09151694A patent/EP2093278A1/de not_active Withdrawn
- 2009-02-02 US US12/363,960 patent/US20100029519A1/en not_active Abandoned
- 2009-02-04 JP JP2009023271A patent/JP2009185287A/ja active Pending
- 2009-02-05 CA CA002652704A patent/CA2652704A1/en not_active Abandoned
- 2009-02-05 CN CNA2009100066101A patent/CN101502770A/zh active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003186138A (ja) * | 2001-11-21 | 2003-07-03 | Eastman Kodak Co | イオン性液体を含む疎水性有機相の分散体を含んで成る組成物 |
JP2005530910A (ja) * | 2002-06-28 | 2005-10-13 | ザ プロクター アンド ギャンブル カンパニー | イオン性液体系製品及びその使用方法 |
JP2007070370A (ja) * | 2004-09-03 | 2007-03-22 | Kansai Paint Co Ltd | 塗料組成物 |
JP2006083211A (ja) * | 2004-09-14 | 2006-03-30 | Shin Etsu Chem Co Ltd | 防汚性縮合硬化型オルガノポリシロキサン組成物及び水中構造物 |
WO2007144286A1 (en) * | 2006-06-14 | 2007-12-21 | Ciba Holding Inc. | Anti-microbial compositions |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016113661A (ja) * | 2014-12-15 | 2016-06-23 | Jfeスチール株式会社 | 連続溶融亜鉛めっき方法及び連続溶融亜鉛めっき設備 |
JP2022510675A (ja) * | 2018-12-04 | 2022-01-27 | エボニック オペレーションズ ゲーエムベーハー | 湿潤ガス混合物の除湿方法 |
JP7206387B2 (ja) | 2018-12-04 | 2023-01-17 | エボニック オペレーションズ ゲーエムベーハー | 湿潤ガス混合物の除湿方法 |
JP7369840B2 (ja) | 2018-12-04 | 2023-10-26 | エボニック オペレーションズ ゲーエムベーハー | 湿潤ガス混合物の除湿方法 |
Also Published As
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CA2652704A1 (en) | 2009-08-05 |
US20100029519A1 (en) | 2010-02-04 |
EP2093278A1 (de) | 2009-08-26 |
CN101502770A (zh) | 2009-08-12 |
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