ZA200504340B - Method for forming functional layers - Google Patents
Method for forming functional layers Download PDFInfo
- Publication number
- ZA200504340B ZA200504340B ZA200504340A ZA200504340A ZA200504340B ZA 200504340 B ZA200504340 B ZA 200504340B ZA 200504340 A ZA200504340 A ZA 200504340A ZA 200504340 A ZA200504340 A ZA 200504340A ZA 200504340 B ZA200504340 B ZA 200504340B
- Authority
- ZA
- South Africa
- Prior art keywords
- group
- acrylate
- acid
- controlling
- properties
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 66
- 239000002346 layers by function Substances 0.000 title claims description 10
- -1 methacryloxyethyl gluco- side Chemical class 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 26
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 24
- 239000000758 substrate Substances 0.000 claims description 24
- 125000000524 functional group Chemical group 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 16
- 239000003999 initiator Substances 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 12
- 239000007789 gas Substances 0.000 claims description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 10
- 239000004952 Polyamide Substances 0.000 claims description 10
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- 239000004721 Polyphenylene oxide Substances 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 7
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- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 6
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 6
- 230000004071 biological effect Effects 0.000 claims description 6
- 238000000576 coating method Methods 0.000 claims description 6
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- 229920000570 polyether Polymers 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
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- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 4
- VBHXIMACZBQHPX-UHFFFAOYSA-N 2,2,2-trifluoroethyl prop-2-enoate Chemical compound FC(F)(F)COC(=O)C=C VBHXIMACZBQHPX-UHFFFAOYSA-N 0.000 claims description 4
- YJKHMSPWWGBKTN-UHFFFAOYSA-N 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluoroheptyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)F YJKHMSPWWGBKTN-UHFFFAOYSA-N 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 4
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 claims description 4
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
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- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
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- 150000008062 acetophenones Chemical class 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 230000012010 growth Effects 0.000 claims description 4
- 125000001165 hydrophobic group Chemical group 0.000 claims description 4
- 229920000515 polycarbonate Polymers 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 230000005855 radiation Effects 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 4
- 229920001059 synthetic polymer Polymers 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 3
- 244000028419 Styrax benzoin Species 0.000 claims description 3
- 235000000126 Styrax benzoin Nutrition 0.000 claims description 3
- 235000008411 Sumatra benzointree Nutrition 0.000 claims description 3
- 150000001241 acetals Chemical class 0.000 claims description 3
- 150000001299 aldehydes Chemical class 0.000 claims description 3
- 150000008064 anhydrides Chemical class 0.000 claims description 3
- 230000003373 anti-fouling effect Effects 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 239000012965 benzophenone Chemical class 0.000 claims description 3
- 150000001642 boronic acid derivatives Chemical class 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 239000000975 dye Substances 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 150000008131 glucosides Chemical class 0.000 claims description 3
- 229920000578 graft copolymer Polymers 0.000 claims description 3
- 235000019382 gum benzoic Nutrition 0.000 claims description 3
- 239000011261 inert gas Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 150000002978 peroxides Chemical class 0.000 claims description 3
- 229920000548 poly(silane) polymer Polymers 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- 229920002635 polyurethane Polymers 0.000 claims description 3
- 239000004065 semiconductor Substances 0.000 claims description 3
- 231100000489 sensitizer Toxicity 0.000 claims description 3
- 150000003568 thioethers Chemical class 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- AIEGYVFQWHGJPT-UHFFFAOYSA-N (1,1,3-tribromo-2,2-dimethylpropyl) 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(Br)(Br)C(C)(C)CBr AIEGYVFQWHGJPT-UHFFFAOYSA-N 0.000 claims description 2
- BKKVYNMMVYEBGR-UHFFFAOYSA-N (2,3,4,5,6-pentabromophenyl) prop-2-enoate Chemical compound BrC1=C(Br)C(Br)=C(OC(=O)C=C)C(Br)=C1Br BKKVYNMMVYEBGR-UHFFFAOYSA-N 0.000 claims description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 2
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 claims description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 2
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 claims description 2
- FWTGTVWNYRCZAI-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCC(OC(=O)C(C)=C)OC(=O)C(C)=C FWTGTVWNYRCZAI-UHFFFAOYSA-N 0.000 claims description 2
- FGFHDNIGKVTTLC-UHFFFAOYSA-N 1-[4-(benzenesulfonyl)phenyl]ethanone Chemical compound C1=CC(C(=O)C)=CC=C1S(=O)(=O)C1=CC=CC=C1 FGFHDNIGKVTTLC-UHFFFAOYSA-N 0.000 claims description 2
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims description 2
- WUIJTQZXUURFQU-UHFFFAOYSA-N 1-methylsulfonylethene Chemical compound CS(=O)(=O)C=C WUIJTQZXUURFQU-UHFFFAOYSA-N 0.000 claims description 2
- PLXOUIVCSUBZIX-UHFFFAOYSA-N 2,2,3,3,4,4,4-heptafluorobutyl prop-2-enoate Chemical compound FC(F)(F)C(F)(F)C(F)(F)COC(=O)C=C PLXOUIVCSUBZIX-UHFFFAOYSA-N 0.000 claims description 2
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 claims description 2
- FTALTLPZDVFJSS-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl prop-2-enoate Chemical compound CCOCCOCCOC(=O)C=C FTALTLPZDVFJSS-UHFFFAOYSA-N 0.000 claims description 2
- PRAMZQXXPOLCIY-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethanesulfonic acid Chemical compound CC(=C)C(=O)OCCS(O)(=O)=O PRAMZQXXPOLCIY-UHFFFAOYSA-N 0.000 claims description 2
- BITAPBDLHJQAID-MDZDMXLPSA-N 2-[2-hydroxyethyl-[(e)-octadec-9-enyl]amino]ethanol Chemical compound CCCCCCCC\C=C\CCCCCCCCN(CCO)CCO BITAPBDLHJQAID-MDZDMXLPSA-N 0.000 claims description 2
- SVYHMICYJHWXIN-UHFFFAOYSA-N 2-[di(propan-2-yl)amino]ethyl 2-methylprop-2-enoate Chemical compound CC(C)N(C(C)C)CCOC(=O)C(C)=C SVYHMICYJHWXIN-UHFFFAOYSA-N 0.000 claims description 2
- NXBXJOWBDCQIHF-UHFFFAOYSA-N 2-[hydroxy-[2-(2-methylprop-2-enoyloxy)ethoxy]phosphoryl]oxyethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOP(O)(=O)OCCOC(=O)C(C)=C NXBXJOWBDCQIHF-UHFFFAOYSA-N 0.000 claims description 2
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- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 2
- PIAOLBVUVDXHHL-UHFFFAOYSA-N 2-nitroethenylbenzene Chemical compound [O-][N+](=O)C=CC1=CC=CC=C1 PIAOLBVUVDXHHL-UHFFFAOYSA-N 0.000 claims description 2
- FMFHUEMLVAIBFI-UHFFFAOYSA-N 2-phenylethenyl acetate Chemical compound CC(=O)OC=CC1=CC=CC=C1 FMFHUEMLVAIBFI-UHFFFAOYSA-N 0.000 claims description 2
- UDXXYUDJOHIIDZ-UHFFFAOYSA-N 2-phosphonooxyethyl prop-2-enoate Chemical compound OP(O)(=O)OCCOC(=O)C=C UDXXYUDJOHIIDZ-UHFFFAOYSA-N 0.000 claims description 2
- JBTDFRNUVWFUGL-UHFFFAOYSA-N 3-aminopropyl carbamimidothioate;dihydrobromide Chemical compound Br.Br.NCCCSC(N)=N JBTDFRNUVWFUGL-UHFFFAOYSA-N 0.000 claims description 2
- NYUTUWAFOUJLKI-UHFFFAOYSA-N 3-prop-2-enoyloxypropane-1-sulfonic acid Chemical compound OS(=O)(=O)CCCOC(=O)C=C NYUTUWAFOUJLKI-UHFFFAOYSA-N 0.000 claims description 2
- VLCHEPDTUQWTPS-UHFFFAOYSA-N 3-prop-2-enoylpyrrolidine-2,5-dione Chemical compound C=CC(=O)C1CC(=O)NC1=O VLCHEPDTUQWTPS-UHFFFAOYSA-N 0.000 claims description 2
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 claims description 2
- YKXAYLPDMSGWEV-UHFFFAOYSA-N 4-hydroxybutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCO YKXAYLPDMSGWEV-UHFFFAOYSA-N 0.000 claims description 2
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 claims description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 2
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- UUEYEUDSRFNIQJ-UHFFFAOYSA-N CCOC(N)=O.CCOC(N)=O.CC(=C)C(O)=O.CC(=C)C(O)=O Chemical compound CCOC(N)=O.CCOC(N)=O.CC(=C)C(O)=O.CC(=C)C(O)=O UUEYEUDSRFNIQJ-UHFFFAOYSA-N 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 2
- 229930194542 Keto Natural products 0.000 claims description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 2
- 125000002355 alkine group Chemical class 0.000 claims description 2
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- 125000000539 amino acid group Chemical group 0.000 claims description 2
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 claims description 2
- 150000008366 benzophenones Chemical class 0.000 claims description 2
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- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
- 230000010261 cell growth Effects 0.000 claims description 2
- 229930016911 cinnamic acid Natural products 0.000 claims description 2
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- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 claims description 2
- 125000004386 diacrylate group Chemical group 0.000 claims description 2
- 239000012954 diazonium Substances 0.000 claims description 2
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- 238000010894 electron beam technology Methods 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 claims description 2
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- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 claims description 2
- FAFWKDXOUWXCDP-UHFFFAOYSA-N ethenylurea Chemical compound NC(=O)NC=C FAFWKDXOUWXCDP-UHFFFAOYSA-N 0.000 claims description 2
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- 125000003827 glycol group Chemical group 0.000 claims description 2
- KUQWZSZYIQGTHT-UHFFFAOYSA-N hexa-1,5-diene-3,4-diol Chemical compound C=CC(O)C(O)C=C KUQWZSZYIQGTHT-UHFFFAOYSA-N 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
- 125000002883 imidazolyl group Chemical group 0.000 claims description 2
- 150000003949 imides Chemical class 0.000 claims description 2
- 125000000468 ketone group Chemical group 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims description 2
- 150000004706 metal oxides Chemical class 0.000 claims description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 2
- OKPYIWASQZGASP-UHFFFAOYSA-N n-(2-hydroxypropyl)-2-methylprop-2-enamide Chemical compound CC(O)CNC(=O)C(C)=C OKPYIWASQZGASP-UHFFFAOYSA-N 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 150000002923 oximes Chemical class 0.000 claims description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 2
- 150000007965 phenolic acids Chemical class 0.000 claims description 2
- PZXHOJFANUNWGC-UHFFFAOYSA-N phenyl 2-oxoacetate Chemical class O=CC(=O)OC1=CC=CC=C1 PZXHOJFANUNWGC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
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DE10260332 | 2002-12-20 | ||
PCT/EP2003/000780 WO2003064061A1 (en) | 2002-01-29 | 2003-01-27 | Process for the production of strongly adherent coatings |
PCT/EP2003/051008 WO2004056496A2 (de) | 2002-12-20 | 2003-12-15 | Verfahren zur ausbildung von funktionsschichten |
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ZA200504340A ZA200504340B (en) | 2002-12-20 | 2005-05-27 | Method for forming functional layers |
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US (1) | US20060246291A1 (es) |
EP (2) | EP1842601B1 (es) |
JP (1) | JP2006511344A (es) |
KR (1) | KR101015033B1 (es) |
CN (1) | CN1726097A (es) |
AU (1) | AU2003299236A1 (es) |
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CA (1) | CA2510359A1 (es) |
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RU (1) | RU2005122903A (es) |
WO (1) | WO2004056496A2 (es) |
ZA (1) | ZA200504340B (es) |
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JP5421533B2 (ja) * | 2004-12-22 | 2014-02-19 | チバ ホールディング インコーポレーテッド | 強接着性コーティングの製造方法 |
JP2006199880A (ja) * | 2005-01-24 | 2006-08-03 | Kuraray Co Ltd | 樹脂成形体の表面改質方法および樹脂成形体 |
WO2007056856A1 (en) * | 2005-11-16 | 2007-05-24 | UNIVERSITé LAVAL | Process for producing anto-fog coating |
US8057852B2 (en) | 2006-11-23 | 2011-11-15 | National Research Council Of Canada | Microdevice for a fluorescence-based assay, and a method for making the microdevice |
US20100178512A1 (en) * | 2006-12-06 | 2010-07-15 | Ciba Corporation | Changing surface properties by functionalized nanoparticles |
US8114465B2 (en) | 2007-04-02 | 2012-02-14 | Ension, Inc. | Process for preparing a substrate coated with a biomolecule |
US9693841B2 (en) | 2007-04-02 | 2017-07-04 | Ension, Inc. | Surface treated staples, sutures and dental floss and methods of manufacturing the same |
WO2010069443A1 (en) * | 2008-12-18 | 2010-06-24 | Merck Patent Gmbh | Process of forming insulating layer by particles having low energy |
KR101174958B1 (ko) * | 2009-09-30 | 2012-08-17 | 코오롱인더스트리 주식회사 | 아라미드 프리프레그의 제조방법 및 아라미드 강판 복합재의 제조방법 |
DE102012007829A1 (de) * | 2012-04-19 | 2013-10-24 | Florian Felix | Antiadhäsionsbeschichtung gegen Schnee und Eis |
WO2013189537A1 (en) * | 2012-06-20 | 2013-12-27 | Allnex Belgium, S.A. | Flame retardant radiation curable compositions |
FR3001642B1 (fr) * | 2013-02-01 | 2016-05-13 | Natvi Sas | Procede de recouvrement de surfaces |
JP6195584B2 (ja) * | 2015-02-04 | 2017-09-13 | 東京応化工業株式会社 | 着色剤分散液、それを含む感光性樹脂組成物、及び分散助剤 |
EP3356140A4 (en) * | 2015-09-30 | 2019-05-08 | 3M Innovative Properties Company | COMPOSITE STRUCTURE WITH GLASS-TYPE LAYER AND METHOD OF FORMING |
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US9732192B1 (en) * | 2016-03-23 | 2017-08-15 | International Business Machines Corporation | Flame-retardant, cross-linked polyhydroxyalkanoate materials |
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CN111282789A (zh) * | 2018-12-07 | 2020-06-16 | 上海航空电器有限公司 | 一种具备隐身性能的编队灯表面涂装前处理方法 |
CN109651942A (zh) * | 2018-12-14 | 2019-04-19 | 江苏盛纳凯尔医用科技有限公司 | 一种超亲水抗菌涂层的制备方法 |
GB2579871B (en) * | 2019-02-22 | 2021-07-14 | P2I Ltd | Coatings |
EP3715406A1 (en) * | 2019-03-29 | 2020-09-30 | Henkel AG & Co. KGaA | Process for modifying the surface polarity of rubber substrates |
CN110205835A (zh) * | 2019-05-31 | 2019-09-06 | 南通东屹高新纤维科技有限公司 | 高强度服装防水面料的制备方法 |
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JP2022537362A (ja) * | 2019-06-18 | 2022-08-25 | モレキュラー・プラズマ・グループ・ソシエテ・アノニム | 抗微生物および/または抗ウイルスポリマー表面 |
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US6387379B1 (en) * | 1987-04-10 | 2002-05-14 | University Of Florida | Biofunctional surface modified ocular implants, surgical instruments, medical devices, prostheses, contact lenses and the like |
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CA2472063C (en) * | 2002-01-29 | 2011-05-24 | Ciba Specialty Chemicals Holding Inc. | Process for the production of strongly adherent coatings |
-
2003
- 2003-12-15 JP JP2005502570A patent/JP2006511344A/ja active Pending
- 2003-12-15 MX MXPA05006693A patent/MXPA05006693A/es active IP Right Grant
- 2003-12-15 AU AU2003299236A patent/AU2003299236A1/en not_active Abandoned
- 2003-12-15 NZ NZ541150A patent/NZ541150A/en not_active IP Right Cessation
- 2003-12-15 EP EP20070103712 patent/EP1842601B1/de not_active Expired - Lifetime
- 2003-12-15 KR KR1020057011655A patent/KR101015033B1/ko not_active IP Right Cessation
- 2003-12-15 RU RU2005122903/12A patent/RU2005122903A/ru not_active Application Discontinuation
- 2003-12-15 BR BR0317587A patent/BR0317587A/pt not_active Application Discontinuation
- 2003-12-15 WO PCT/EP2003/051008 patent/WO2004056496A2/de active Application Filing
- 2003-12-15 CA CA 2510359 patent/CA2510359A1/en not_active Abandoned
- 2003-12-15 CN CNA2003801064956A patent/CN1726097A/zh active Pending
- 2003-12-15 EP EP03799569A patent/EP1572379A2/de not_active Withdrawn
- 2003-12-15 US US10/538,893 patent/US20060246291A1/en not_active Abandoned
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2005
- 2005-05-27 ZA ZA200504340A patent/ZA200504340B/en unknown
Also Published As
Publication number | Publication date |
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EP1842601B1 (de) | 2009-07-22 |
EP1842601A1 (de) | 2007-10-10 |
WO2004056496A3 (de) | 2004-09-23 |
KR101015033B1 (ko) | 2011-02-16 |
EP1572379A2 (de) | 2005-09-14 |
WO2004056496A2 (de) | 2004-07-08 |
RU2005122903A (ru) | 2006-08-10 |
AU2003299236A1 (en) | 2004-07-14 |
CN1726097A (zh) | 2006-01-25 |
KR20050100364A (ko) | 2005-10-18 |
CA2510359A1 (en) | 2004-07-08 |
JP2006511344A (ja) | 2006-04-06 |
BR0317587A (pt) | 2005-11-22 |
MXPA05006693A (es) | 2005-09-08 |
US20060246291A1 (en) | 2006-11-02 |
NZ541150A (en) | 2008-03-28 |
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