KR20070114190A - (메트)아크릴 기 함유 퍼플루오로폴리에테르 우레탄 첨가제및 하드코트 - Google Patents
(메트)아크릴 기 함유 퍼플루오로폴리에테르 우레탄 첨가제및 하드코트 Download PDFInfo
- Publication number
- KR20070114190A KR20070114190A KR1020077021774A KR20077021774A KR20070114190A KR 20070114190 A KR20070114190 A KR 20070114190A KR 1020077021774 A KR1020077021774 A KR 1020077021774A KR 20077021774 A KR20077021774 A KR 20077021774A KR 20070114190 A KR20070114190 A KR 20070114190A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- composition
- meth
- perfluoropolyether
- urethane
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 239000000654 additive Substances 0.000 title claims abstract description 34
- 239000010702 perfluoropolyether Substances 0.000 title claims description 98
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 title claims description 65
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims description 39
- 230000003287 optical effect Effects 0.000 claims abstract description 57
- 239000002344 surface layer Substances 0.000 claims abstract description 24
- 239000000203 mixture Substances 0.000 claims description 148
- -1 acryl groups Chemical group 0.000 claims description 63
- 150000001875 compounds Chemical class 0.000 claims description 48
- 239000000463 material Substances 0.000 claims description 47
- 239000002245 particle Substances 0.000 claims description 47
- 239000010410 layer Substances 0.000 claims description 43
- 238000000034 method Methods 0.000 claims description 42
- 239000000758 substrate Substances 0.000 claims description 39
- 125000004432 carbon atom Chemical group C* 0.000 claims description 36
- 229910052757 nitrogen Inorganic materials 0.000 claims description 36
- 239000007787 solid Substances 0.000 claims description 34
- 125000005842 heteroatom Chemical group 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 229910052760 oxygen Inorganic materials 0.000 claims description 26
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 25
- 125000002947 alkylene group Chemical group 0.000 claims description 24
- 229910052731 fluorine Inorganic materials 0.000 claims description 24
- 229910052717 sulfur Inorganic materials 0.000 claims description 24
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 23
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 23
- 125000005647 linker group Chemical group 0.000 claims description 22
- 229930195733 hydrocarbon Natural products 0.000 claims description 21
- 239000004215 Carbon black (E152) Substances 0.000 claims description 20
- 150000002430 hydrocarbons Chemical class 0.000 claims description 20
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 19
- 229910052809 inorganic oxide Inorganic materials 0.000 claims description 19
- 239000012948 isocyanate Substances 0.000 claims description 19
- 239000011737 fluorine Substances 0.000 claims description 17
- 230000000996 additive effect Effects 0.000 claims description 14
- 239000008199 coating composition Substances 0.000 claims description 14
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 14
- 125000000524 functional group Chemical group 0.000 claims description 14
- 239000004971 Cross linker Substances 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 125000000732 arylene group Chemical group 0.000 claims description 12
- 239000006224 matting agent Substances 0.000 claims description 11
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 10
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 10
- 150000001408 amides Chemical class 0.000 claims description 9
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 9
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 9
- 239000007795 chemical reaction product Substances 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 8
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 7
- 125000004474 heteroalkylene group Chemical group 0.000 claims description 7
- 230000001681 protective effect Effects 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 7
- 150000007970 thio esters Chemical class 0.000 claims description 7
- 150000003573 thiols Chemical class 0.000 claims description 7
- 150000003673 urethanes Chemical class 0.000 claims description 7
- 229910044991 metal oxide Inorganic materials 0.000 claims description 6
- 150000004706 metal oxides Chemical class 0.000 claims description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
- 239000002105 nanoparticle Substances 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 3
- 229920006295 polythiol Chemical class 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000012790 adhesive layer Substances 0.000 claims description 2
- 125000000962 organic group Chemical group 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 125000003368 amide group Chemical group 0.000 claims 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 75
- 238000004519 manufacturing process Methods 0.000 description 64
- 238000000576 coating method Methods 0.000 description 59
- 239000011248 coating agent Substances 0.000 description 48
- 239000000243 solution Substances 0.000 description 48
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 description 42
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 40
- 239000010408 film Substances 0.000 description 35
- 238000006243 chemical reaction Methods 0.000 description 33
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 23
- 238000003756 stirring Methods 0.000 description 23
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 20
- 239000012975 dibutyltin dilaurate Substances 0.000 description 20
- 239000000047 product Substances 0.000 description 19
- 239000003054 catalyst Substances 0.000 description 18
- 239000003921 oil Substances 0.000 description 18
- 238000004458 analytical method Methods 0.000 description 17
- 239000000126 substance Substances 0.000 description 17
- 238000012360 testing method Methods 0.000 description 17
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 16
- 238000002360 preparation method Methods 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 14
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 14
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 13
- 239000007788 liquid Substances 0.000 description 12
- 229920000058 polyacrylate Polymers 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000009472 formulation Methods 0.000 description 10
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 229940096522 trimethylolpropane triacrylate Drugs 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 150000002513 isocyanates Chemical class 0.000 description 9
- 239000004576 sand Substances 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 239000012788 optical film Substances 0.000 description 8
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 7
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 description 7
- 239000005020 polyethylene terephthalate Substances 0.000 description 7
- 230000003068 static effect Effects 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 150000002009 diols Chemical class 0.000 description 6
- 238000009826 distribution Methods 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 229920002313 fluoropolymer Polymers 0.000 description 6
- 239000003999 initiator Substances 0.000 description 6
- 239000010954 inorganic particle Substances 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 235000019439 ethyl acetate Nutrition 0.000 description 5
- 230000004927 fusion Effects 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 241001422033 Thestylus Species 0.000 description 4
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 4
- FHLPGTXWCFQMIU-UHFFFAOYSA-N [4-[2-(4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical compound C=1C=C(OC(=O)C=C)C=CC=1C(C)(C)C1=CC=C(OC(=O)C=C)C=C1 FHLPGTXWCFQMIU-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 230000003667 anti-reflective effect Effects 0.000 description 4
- 239000011247 coating layer Substances 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 238000007607 die coating method Methods 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 4
- 239000004811 fluoropolymer Substances 0.000 description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 150000004702 methyl esters Chemical class 0.000 description 4
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 238000005191 phase separation Methods 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 239000006188 syrup Substances 0.000 description 4
- 235000020357 syrup Nutrition 0.000 description 4
- 210000001519 tissue Anatomy 0.000 description 4
- 238000002834 transmittance Methods 0.000 description 4
- XYQNMGJZDSSVRP-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(2-hydroxyethyl)butane-1-sulfonamide Chemical compound OCCN(CCO)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F XYQNMGJZDSSVRP-UHFFFAOYSA-N 0.000 description 3
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 3
- UHFFVFAKEGKNAQ-UHFFFAOYSA-N 2-benzyl-2-(dimethylamino)-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=CC=C1 UHFFVFAKEGKNAQ-UHFFFAOYSA-N 0.000 description 3
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 3
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 238000004508 fractional distillation Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 3
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 2
- PCLLJCFJFOBGDE-UHFFFAOYSA-N (5-bromo-2-chlorophenyl)methanamine Chemical compound NCC1=CC(Br)=CC=C1Cl PCLLJCFJFOBGDE-UHFFFAOYSA-N 0.000 description 2
- DSRUAYIFDCHEEV-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,4-nonafluoro-n-(2-hydroxyethyl)-n-methylbutane-1-sulfonamide Chemical compound OCCN(C)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F DSRUAYIFDCHEEV-UHFFFAOYSA-N 0.000 description 2
- PUGOMSLRUSTQGV-UHFFFAOYSA-N 2,3-di(prop-2-enoyloxy)propyl prop-2-enoate Chemical compound C=CC(=O)OCC(OC(=O)C=C)COC(=O)C=C PUGOMSLRUSTQGV-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
- IOAOAKDONABGPZ-UHFFFAOYSA-N 2-amino-2-ethylpropane-1,3-diol Chemical compound CCC(N)(CO)CO IOAOAKDONABGPZ-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 2
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000003373 anti-fouling effect Effects 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000004386 diacrylate group Chemical group 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000003670 easy-to-clean Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000001815 facial effect Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- RCGIUOVPEJGLGD-UHFFFAOYSA-N imidazolidine-2,4-dione;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.O=C1CNC(=O)N1 RCGIUOVPEJGLGD-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 239000003550 marker Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920001690 polydopamine Polymers 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- NNJPGOLRFBJNIW-HNNXBMFYSA-N (-)-demecolcine Chemical compound C1=C(OC)C(=O)C=C2[C@@H](NC)CCC3=CC(OC)=C(OC)C(OC)=C3C2=C1 NNJPGOLRFBJNIW-HNNXBMFYSA-N 0.000 description 1
- DZZAHYHMWKNGLC-UHFFFAOYSA-N (1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexyl)methyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C1(F)F DZZAHYHMWKNGLC-UHFFFAOYSA-N 0.000 description 1
- UDKYUCSMIYESKQ-UHFFFAOYSA-N (2,2,3,3,4,4,5,5-octafluoro-1-prop-2-enoyloxyhexyl) prop-2-enoate Chemical compound CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(OC(=O)C=C)OC(=O)C=C UDKYUCSMIYESKQ-UHFFFAOYSA-N 0.000 description 1
- OKIYQFLILPKULA-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4-nonafluoro-4-methoxybutane Chemical compound COC(F)(F)C(F)(F)C(F)(F)C(F)(F)F OKIYQFLILPKULA-UHFFFAOYSA-N 0.000 description 1
- DPLWOKBNTLXZKL-UHFFFAOYSA-N 1-[2-(2-aminoethoxy)ethoxy]ethanol Chemical compound NCCOCCOC(C)O DPLWOKBNTLXZKL-UHFFFAOYSA-N 0.000 description 1
- ZDQNWDNMNKSMHI-UHFFFAOYSA-N 1-[2-(2-prop-2-enoyloxypropoxy)propoxy]propan-2-yl prop-2-enoate Chemical compound C=CC(=O)OC(C)COC(C)COCC(C)OC(=O)C=C ZDQNWDNMNKSMHI-UHFFFAOYSA-N 0.000 description 1
- LUVYSKHTFMLGSA-UHFFFAOYSA-N 1-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethanol Chemical compound NCCOCCOCCOC(C)O LUVYSKHTFMLGSA-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
- VPMMJSPGZSFEAH-UHFFFAOYSA-N 2,4-diaminophenol;hydrochloride Chemical compound [Cl-].NC1=CC=C(O)C([NH3+])=C1 VPMMJSPGZSFEAH-UHFFFAOYSA-N 0.000 description 1
- YIJYFLXQHDOQGW-UHFFFAOYSA-N 2-[2,4,6-trioxo-3,5-bis(2-prop-2-enoyloxyethyl)-1,3,5-triazinan-1-yl]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCN1C(=O)N(CCOC(=O)C=C)C(=O)N(CCOC(=O)C=C)C1=O YIJYFLXQHDOQGW-UHFFFAOYSA-N 0.000 description 1
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 description 1
- DZZAHLOABNWIFA-UHFFFAOYSA-N 2-butoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCCCC)C(=O)C1=CC=CC=C1 DZZAHLOABNWIFA-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- TYCFGHUTYSLISP-UHFFFAOYSA-N 2-fluoroprop-2-enoic acid Chemical class OC(=O)C(F)=C TYCFGHUTYSLISP-UHFFFAOYSA-N 0.000 description 1
- CKKQLOUBFINSIB-UHFFFAOYSA-N 2-hydroxy-1,2,2-triphenylethanone Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C(=O)C1=CC=CC=C1 CKKQLOUBFINSIB-UHFFFAOYSA-N 0.000 description 1
- YOJAHTBCSGPSOR-UHFFFAOYSA-N 2-hydroxy-1,2,3-triphenylpropan-1-one Chemical compound C=1C=CC=CC=1C(=O)C(C=1C=CC=CC=1)(O)CC1=CC=CC=C1 YOJAHTBCSGPSOR-UHFFFAOYSA-N 0.000 description 1
- RZCDMINQJLGWEP-UHFFFAOYSA-N 2-hydroxy-1,2-diphenylpent-4-en-1-one Chemical compound C=1C=CC=CC=1C(CC=C)(O)C(=O)C1=CC=CC=C1 RZCDMINQJLGWEP-UHFFFAOYSA-N 0.000 description 1
- DIVXVZXROTWKIH-UHFFFAOYSA-N 2-hydroxy-1,2-diphenylpropan-1-one Chemical compound C=1C=CC=CC=1C(O)(C)C(=O)C1=CC=CC=C1 DIVXVZXROTWKIH-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- ZPQAUEDTKNBRNG-UHFFFAOYSA-N 2-methylprop-2-enoylsilicon Chemical compound CC(=C)C([Si])=O ZPQAUEDTKNBRNG-UHFFFAOYSA-N 0.000 description 1
- KTALPKYXQZGAEG-UHFFFAOYSA-N 2-propan-2-ylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=C1 KTALPKYXQZGAEG-UHFFFAOYSA-N 0.000 description 1
- FQMIAEWUVYWVNB-UHFFFAOYSA-N 3-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OC(C)CCOC(=O)C=C FQMIAEWUVYWVNB-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- SUTWPJHCRAITLU-UHFFFAOYSA-N 6-aminohexan-1-ol Chemical compound NCCCCCCO SUTWPJHCRAITLU-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- IMJLWKZFJOIXJL-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C=C IMJLWKZFJOIXJL-UHFFFAOYSA-N 0.000 description 1
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Divinylene sulfide Natural products C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 229920002633 Kraton (polymer) Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 229920001774 Perfluoroether Chemical group 0.000 description 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 108091092920 SmY RNA Proteins 0.000 description 1
- 241001237710 Smyrna Species 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- 206010047571 Visual impairment Diseases 0.000 description 1
- LFOXEOLGJPJZAA-UHFFFAOYSA-N [(2,6-dimethoxybenzoyl)-(2,4,4-trimethylpentyl)phosphoryl]-(2,6-dimethoxyphenyl)methanone Chemical compound COC1=CC=CC(OC)=C1C(=O)P(=O)(CC(C)CC(C)(C)C)C(=O)C1=C(OC)C=CC=C1OC LFOXEOLGJPJZAA-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- XRMBQHTWUBGQDN-UHFFFAOYSA-N [2-[2,2-bis(prop-2-enoyloxymethyl)butoxymethyl]-2-(prop-2-enoyloxymethyl)butyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(CC)COCC(CC)(COC(=O)C=C)COC(=O)C=C XRMBQHTWUBGQDN-UHFFFAOYSA-N 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- VEBCLRKUSAGCDF-UHFFFAOYSA-N ac1mi23b Chemical compound C1C2C3C(COC(=O)C=C)CCC3C1C(COC(=O)C=C)C2 VEBCLRKUSAGCDF-UHFFFAOYSA-N 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000004931 aggregating effect Effects 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005012 alkyl thioether group Chemical group 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 150000008365 aromatic ketones Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 description 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- CWZPGMMKDANPKU-UHFFFAOYSA-L butyl-di(dodecanoyloxy)tin Chemical compound CCCC[Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O CWZPGMMKDANPKU-UHFFFAOYSA-L 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000011097 chromatography purification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000001246 colloidal dispersion Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000011370 conductive nanoparticle Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000003818 flash chromatography Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000012949 free radical photoinitiator Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000008131 herbal destillate Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical group O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229940104873 methyl perfluorobutyl ether Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QHJABUZHRJTCAR-UHFFFAOYSA-N n'-methylpropane-1,3-diamine Chemical compound CNCCCN QHJABUZHRJTCAR-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- UJMWVICAENGCRF-UHFFFAOYSA-N oxygen difluoride Chemical group FOF UJMWVICAENGCRF-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000006551 perfluoro alkylene group Chemical group 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- FSDNTQSJGHSJBG-UHFFFAOYSA-N piperidine-4-carbonitrile Chemical compound N#CC1CCNCC1 FSDNTQSJGHSJBG-UHFFFAOYSA-N 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- SKRWFPLZQAAQSU-UHFFFAOYSA-N stibanylidynetin;hydrate Chemical compound O.[Sn].[Sb] SKRWFPLZQAAQSU-UHFFFAOYSA-N 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 239000013077 target material Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- 150000003608 titanium Chemical class 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 238000013024 troubleshooting Methods 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 208000029257 vision disease Diseases 0.000 description 1
- 230000004393 visual impairment Effects 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 210000000707 wrist Anatomy 0.000 description 1
- OWOMRZKBDFBMHP-UHFFFAOYSA-N zinc antimony(3+) oxygen(2-) Chemical compound [O--].[Zn++].[Sb+3] OWOMRZKBDFBMHP-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/067—Polyurethanes; Polyureas
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/08—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/2885—Compounds containing at least one heteroatom other than oxygen or nitrogen containing halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/289—Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3802—Low-molecular-weight compounds having heteroatoms other than oxygen having halogens
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
- C08G18/3823—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing -N-C=O groups
- C08G18/3825—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing -N-C=O groups containing amide groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
- C08G18/673—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen containing two or more acrylate or alkylacrylate ester groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/7806—Nitrogen containing -N-C=0 groups
- C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
- C08G18/7831—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing biuret groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/81—Unsaturated isocyanates or isothiocyanates
- C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
- C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
- C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
- C08G18/8175—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09D175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
-
- G02B1/105—
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/14—Protective coatings, e.g. hard coatings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
- Y10T428/264—Up to 3 mils
- Y10T428/265—1 mil or less
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Physics & Mathematics (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Optics & Photonics (AREA)
- General Physics & Mathematics (AREA)
- Paints Or Removers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Laminated Bodies (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/087,413 US20060216524A1 (en) | 2005-03-23 | 2005-03-23 | Perfluoropolyether urethane additives having (meth)acryl groups and hard coats |
| US11/087,413 | 2005-03-23 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137013814A Division KR101397831B1 (ko) | 2005-03-23 | 2006-03-22 | (메트)아크릴 기 함유 퍼플루오로폴리에테르 우레탄 첨가제 및 하드코트 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20070114190A true KR20070114190A (ko) | 2007-11-29 |
Family
ID=36645694
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020077021774A Ceased KR20070114190A (ko) | 2005-03-23 | 2006-03-22 | (메트)아크릴 기 함유 퍼플루오로폴리에테르 우레탄 첨가제및 하드코트 |
| KR1020137013814A Expired - Fee Related KR101397831B1 (ko) | 2005-03-23 | 2006-03-22 | (메트)아크릴 기 함유 퍼플루오로폴리에테르 우레탄 첨가제 및 하드코트 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137013814A Expired - Fee Related KR101397831B1 (ko) | 2005-03-23 | 2006-03-22 | (메트)아크릴 기 함유 퍼플루오로폴리에테르 우레탄 첨가제 및 하드코트 |
Country Status (7)
| Country | Link |
|---|---|
| US (6) | US20060216524A1 (enExample) |
| EP (1) | EP1866355B1 (enExample) |
| JP (1) | JP5118017B2 (enExample) |
| KR (2) | KR20070114190A (enExample) |
| CN (1) | CN101146840B (enExample) |
| TW (1) | TWI412779B (enExample) |
| WO (1) | WO2006102383A1 (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9207911B2 (en) | 2009-07-31 | 2015-12-08 | Cassy Holdings Llc | Modular uncertainty random value generator and method |
| US9292259B2 (en) | 2008-08-06 | 2016-03-22 | Cassy Holdings Llc | Uncertainty random value generator |
| KR20160108716A (ko) * | 2015-03-05 | 2016-09-20 | (주)엘지하우시스 | 인덱스매칭 필름 |
| US9990180B2 (en) | 2011-05-27 | 2018-06-05 | Cassy Holdings Llc | Stochastic processing |
Families Citing this family (200)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8617715B2 (en) * | 2003-12-06 | 2013-12-31 | Cpfilms Inc. | Fire retardant shades |
| US20060216524A1 (en) | 2005-03-23 | 2006-09-28 | 3M Innovative Properties Company | Perfluoropolyether urethane additives having (meth)acryl groups and hard coats |
| US7759447B2 (en) | 2005-11-17 | 2010-07-20 | Bayer Materialscience Llc | Low surface energy, ethylenically unsaturated polyisocyanate addition compounds and their use in coating compositions |
| KR101257136B1 (ko) | 2006-01-12 | 2013-04-23 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 집광 필름 |
| US7413807B2 (en) * | 2006-04-14 | 2008-08-19 | 3M Innovative Properties Company | Fluoroalkyl silicone composition |
| US7410704B2 (en) * | 2006-04-14 | 2008-08-12 | 3M Innovative Properties Company | Composition containing fluoroalkyl hydrosilicone |
| US7407710B2 (en) * | 2006-04-14 | 2008-08-05 | 3M Innovative Properties Company | Composition containing fluoroalkyl silicone and hydrosilicone |
| US20070285779A1 (en) * | 2006-06-13 | 2007-12-13 | Walker Christopher B | Optical films comprising high refractive index and antireflective coatings |
| US7575847B2 (en) * | 2006-06-13 | 2009-08-18 | 3M Innovative Properties Company | Low refractive index composition comprising fluoropolyether urethane compound |
| US7537828B2 (en) * | 2006-06-13 | 2009-05-26 | 3M Innovative Properties Company | Low refractive index composition comprising fluoropolyether urethane compound |
| US20070285778A1 (en) * | 2006-06-13 | 2007-12-13 | Walker Christopher B | Optical films comprising high refractive index and antireflective coatings |
| US20070292679A1 (en) * | 2006-06-14 | 2007-12-20 | 3M Innovative Properties Company | Optical article having an antistatic fluorochemical surface layer |
| JP5220286B2 (ja) * | 2006-06-15 | 2013-06-26 | 日東電工株式会社 | 防眩性ハードコートフィルム、それを用いた偏光板および画像表示装置 |
| US20080075951A1 (en) * | 2006-09-27 | 2008-03-27 | 3M Innovative Properties Company | Fluoroacrylates and hardcoat compositions including the same |
| US8530054B2 (en) * | 2006-09-27 | 2013-09-10 | 3M Innovative Properties Company | Solar control multilayer film |
| US20080124555A1 (en) | 2006-11-29 | 2008-05-29 | 3M Innovative Properties Company | Polymerizable composition comprising perfluoropolyether urethane having ethylene oxide repeat units |
| US8002886B2 (en) * | 2006-12-15 | 2011-08-23 | 3M Innovative Properties Company | Fluorochemical urethane compounds having pendent silyl groups used for surface treatment |
| CN101563383B (zh) * | 2006-12-20 | 2012-08-15 | 3M创新有限公司 | 具有侧链甲硅烷基的含氟氨基甲酸酯化合物 |
| US7745653B2 (en) * | 2007-03-08 | 2010-06-29 | 3M Innovative Properties Company | Fluorochemical compounds having pendent silyl groups |
| US8206827B2 (en) * | 2007-03-15 | 2012-06-26 | Nanovere Technologies, Llc | Dendritic polyurethane coating |
| US8568888B2 (en) | 2007-03-15 | 2013-10-29 | Nanovere Technologies, Inc. | Dendritic polyurethane coating |
| US7335786B1 (en) | 2007-03-29 | 2008-02-26 | 3M Innovative Properties Company | Michael-adduct fluorochemical silanes |
| US20080274352A1 (en) * | 2007-05-04 | 2008-11-06 | 3M Innovative Properties Company | Optical film comprising antistatic primer and antistatic compositions |
| US7652117B2 (en) * | 2007-06-20 | 2010-01-26 | 3M Innovative Properties Company | Fluorochemical urethane compounds and aqueous compositions thereof |
| US7652116B2 (en) * | 2007-06-20 | 2010-01-26 | 3M Innovative Properties Company | Fluorochemical urethane-silane compounds and aqueous compositions thereof |
| US7897678B2 (en) * | 2007-07-26 | 2011-03-01 | 3M Innovative Properties Company | Fluorochemical urethane compounds having pendent silyl groups |
| US8015970B2 (en) | 2007-07-26 | 2011-09-13 | 3M Innovative Properties Company | Respirator, welding helmet, or face shield that has low surface energy hard-coat lens |
| WO2009029438A1 (en) | 2007-08-31 | 2009-03-05 | 3M Innovative Properties Company | Hardcoats |
| US20090148654A1 (en) * | 2007-12-06 | 2009-06-11 | E. I. Du Pont De Nemours And Company | Fluoropolymer compositions and treated substrates |
| US20090148653A1 (en) * | 2007-12-07 | 2009-06-11 | E.I. Du Pont De Nemours And Company | Fluoropolymer emulsions |
| US8628855B2 (en) * | 2007-12-12 | 2014-01-14 | 3M Innovative Properties Company | Hardcoats comprising perfluoropolyether polymers with poly(alkylene oxide) repeat units |
| US20090181242A1 (en) * | 2008-01-11 | 2009-07-16 | Enniss James P | Exterior window film |
| US9893337B2 (en) | 2008-02-13 | 2018-02-13 | Seeo, Inc. | Multi-phase electrolyte lithium batteries |
| US8563221B2 (en) * | 2008-03-11 | 2013-10-22 | 3M Innovative Properties Company | Phototools having a protective layer |
| JP2011516921A (ja) * | 2008-03-31 | 2011-05-26 | スリーエム イノベイティブ プロパティズ カンパニー | 光学フィルム |
| JP2011516920A (ja) * | 2008-03-31 | 2011-05-26 | スリーエム イノベイティブ プロパティズ カンパニー | 最適化された利得の低層数反射型偏光子 |
| CN102123837B (zh) | 2008-06-20 | 2014-07-09 | 3M创新有限公司 | 聚合物模具和由其制成的制品 |
| JP5681104B2 (ja) | 2008-07-10 | 2015-03-04 | スリーエム イノベイティブ プロパティズ カンパニー | 粘弾性導光体を有する再帰反射物品及びデバイス |
| JP5539980B2 (ja) * | 2008-07-10 | 2014-07-02 | スリーエム イノベイティブ プロパティズ カンパニー | 粘弾性光ガイドを有する再帰反射物品及び装置 |
| EP2313800A4 (en) | 2008-07-10 | 2014-03-19 | 3M Innovative Properties Co | VISCOELASTIC LIGHT GUIDE |
| EP3026471A1 (en) | 2008-08-08 | 2016-06-01 | 3M Innovative Properties Company | Lightguide having a viscoelastic layer for managing light |
| EP2370269B1 (en) | 2008-12-11 | 2015-08-05 | 3M Innovative Properties Company | Patterning process |
| KR101041240B1 (ko) * | 2009-02-27 | 2011-06-14 | 주식회사 엘지화학 | 내마모성 및 내오염성이 우수한 코팅 조성물 및 코팅 필름 |
| KR101145582B1 (ko) * | 2009-03-23 | 2012-05-15 | 디아이씨 가부시끼가이샤 | 보호 점착 필름, 스크린 패널, 및 휴대 전자 단말기 |
| KR101103409B1 (ko) | 2009-03-24 | 2012-01-05 | 제일모직주식회사 | 고광택 곡면 장식 패널 및 그 제조방법 |
| JP5656431B2 (ja) * | 2009-03-31 | 2015-01-21 | 富士フイルム株式会社 | 反射防止フィルム、偏光板、画像表示装置、及び低屈折率層形成用塗布組成物 |
| US20100252376A1 (en) * | 2009-04-02 | 2010-10-07 | Ford Global Technologies Llc | Vehicle Braking Assembly |
| CN102804061A (zh) * | 2009-05-08 | 2012-11-28 | 惠普开发有限公司 | 作为疏水性涂层的功能化全氟聚醚材料 |
| TWI476223B (zh) * | 2009-06-16 | 2015-03-11 | Mitsubishi Rayon Co | 防污組成物、防污膜、防污積層膜、轉印薄膜及樹脂積層體以及樹脂積層體的製造方法 |
| CN102597116B (zh) | 2009-07-21 | 2013-12-11 | 3M创新有限公司 | 可固化组合物、涂覆底片的方法、以及被涂覆的底片 |
| US8564310B2 (en) | 2009-08-18 | 2013-10-22 | 3M Innovative Properties Company | Capacitive oil quality monitoring sensor with fluorinated barrier coating |
| EP2467086B1 (en) | 2009-08-21 | 2016-10-26 | 3M Innovative Properties Company | Kits and products for reducing tissue trauma using water-resistant stress-distributing materials |
| CN102625677B (zh) | 2009-08-21 | 2016-05-18 | 3M创新有限公司 | 使用吸水性应力分布材料来减轻组织创伤的方法和产品 |
| WO2011022525A1 (en) | 2009-08-21 | 2011-02-24 | 3M Innovative Properties Company | Methods and products for illuminating tissue |
| EP2470509A2 (en) | 2009-08-28 | 2012-07-04 | 3M Innovative Properties Company | Compositions and articles comprising polymerizable ionic liquid mixture, and methods of curing |
| KR101783062B1 (ko) | 2009-08-28 | 2017-09-28 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 다작용성 양이온을 포함하는 중합성 이온성 액체 및 정전기 방지 코팅 |
| EP2470929B1 (en) | 2009-08-28 | 2018-06-27 | 3M Innovative Properties Company | Optical device with antistatic coating |
| US8492454B2 (en) | 2009-10-05 | 2013-07-23 | Creative Nail Design, Inc. | Removable color layer for artificial nail coatings and methods therefore |
| US8263677B2 (en) * | 2009-09-08 | 2012-09-11 | Creative Nail Design, Inc. | Removable color gel basecoat for artificial nail coatings and methods therefore |
| US8541482B2 (en) | 2009-10-05 | 2013-09-24 | Creative Nail Design, Inc. | Removable multilayer nail coating system and methods therefore |
| US8420281B2 (en) * | 2009-09-16 | 2013-04-16 | 3M Innovative Properties Company | Epoxy-functionalized perfluoropolyether polyurethanes |
| US9051423B2 (en) | 2009-09-16 | 2015-06-09 | 3M Innovative Properties Company | Fluorinated coating and phototools made therewith |
| EP2478033A1 (en) | 2009-09-16 | 2012-07-25 | 3M Innovative Properties Company | Fluorinated coating and phototools made therewith |
| US8899957B2 (en) | 2009-09-25 | 2014-12-02 | HGST Netherlands B.V. | System, method and apparatus for manufacturing magnetic recording media |
| GB0919014D0 (en) | 2009-10-30 | 2009-12-16 | 3M Innovative Properties Co | Soll and stain resistant coating composition for finished leather substrates |
| US8507601B2 (en) * | 2009-11-09 | 2013-08-13 | E. I. Du Pont De Nemours And Company | Method using fluoropolymer emulsions |
| US8329822B2 (en) * | 2009-11-09 | 2012-12-11 | E.I. Du Pont De Nemours And Company | Fluoropolymer emulsions |
| RU2012131166A (ru) | 2009-12-22 | 2014-01-27 | 3М Инновейтив Пропертиз Компани | Отверждаемые стоматологические композиции и изделия, содержащие полимеризуемые ионные жидкости |
| EP2524252A2 (en) | 2010-01-13 | 2012-11-21 | 3M Innovative Properties Company | Illumination device having viscoelastic lightguide |
| EP2534509B1 (en) | 2010-02-10 | 2019-07-24 | 3M Innovative Properties Company | Illumination device having viscoelastic layer |
| US20130149525A1 (en) * | 2010-03-31 | 2013-06-13 | Toray Advanced Film Co., Ltd. | Surface protection film |
| WO2012050663A1 (en) | 2010-10-11 | 2012-04-19 | 3M Innovative Properties Company | Illumination device having viscoelastic lightguide |
| JP5625836B2 (ja) * | 2010-12-03 | 2014-11-19 | 横浜ゴム株式会社 | 硬化性樹脂組成物 |
| US20120148846A1 (en) * | 2010-12-10 | 2012-06-14 | Ppg Industries Ohio, Inc. | Color plus clear coating systems exhibiting desirable appearance and fingerprint resistance properties and related methods |
| US20120148848A1 (en) * | 2010-12-10 | 2012-06-14 | Martin David C | Polymeric substrates having a thin metal film and fingerprint resistant clear coating deposited thereon and related methods |
| US9296904B2 (en) | 2010-12-20 | 2016-03-29 | 3M Innovative Properties Company | Coating compositions comprising non-ionic surfactant exhibiting reduced fingerprint visibility |
| US8742022B2 (en) | 2010-12-20 | 2014-06-03 | 3M Innovative Properties Company | Coating compositions comprising non-ionic surfactant exhibiting reduced fingerprint visibility |
| CN103403073B (zh) | 2011-02-03 | 2015-10-14 | 3M创新有限公司 | 硬涂膜 |
| KR20140016315A (ko) | 2011-03-07 | 2014-02-07 | 크리에이티브 네일 디자인 인코포레이티드 | Uv-경화성 미용 손톱 코팅제를 위한 조성물 및 방법 |
| US9310527B2 (en) | 2011-03-09 | 2016-04-12 | 3M Innovative Properties Company | Antireflective film comprising large particle size fumed silica |
| US8999509B2 (en) | 2011-04-27 | 2015-04-07 | Cpfilms Inc. | Weather resistant exterior film composite |
| WO2012162041A2 (en) | 2011-05-20 | 2012-11-29 | 3M Innovative Properties Company | Laser-personalizable security articles |
| EP2710519B1 (en) | 2011-05-20 | 2019-07-17 | Gemalto SA | Laser-personalized security articles |
| JP2013076029A (ja) * | 2011-09-30 | 2013-04-25 | Tdk Corp | ハードコート剤組成物及びこれを用いたハードコートフィルム |
| WO2013116032A1 (en) | 2012-01-31 | 2013-08-08 | 3M Innovative Properties Company | Methods for sealing the edges of multi-layer articles |
| KR20140130150A (ko) | 2012-02-03 | 2014-11-07 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 광학 필름용 프라이머 조성물 |
| US8715904B2 (en) * | 2012-04-27 | 2014-05-06 | 3M Innovative Properties Company | Photocurable composition |
| JP6363072B2 (ja) | 2012-06-19 | 2018-07-25 | スリーエム イノベイティブ プロパティズ カンパニー | 低表面エネルギー基及びヒドロキシル基を含む添加剤、並びにコーティング組成物 |
| WO2013191822A1 (en) | 2012-06-19 | 2013-12-27 | 3M Innovative Properties Company | Coating compositions comprising polymerizable non-ionic surfactant exhibiting reduced fingerprint visibility |
| US9346975B2 (en) | 2012-06-29 | 2016-05-24 | 3M Innovative Properties Company | Silsesquioxane-like particles |
| WO2014011731A1 (en) | 2012-07-13 | 2014-01-16 | 3M Innovative Properties Company | Hardcoats comprising alkoxylated multi (meth)acrylate monomers |
| JP6371032B2 (ja) * | 2012-08-01 | 2018-08-08 | スリーエム イノベイティブ プロパティズ カンパニー | 反射防止ハードコートおよび反射防止物品 |
| JP6062680B2 (ja) * | 2012-08-01 | 2017-01-18 | スリーエム イノベイティブ プロパティズ カンパニー | 防汚性ハードコートおよび防汚性ハードコート前駆体 |
| EP2883109A1 (en) | 2012-08-09 | 2015-06-17 | 3M Innovative Properties Company | Photocurable compositions |
| US8883402B2 (en) | 2012-08-09 | 2014-11-11 | 3M Innovative Properties Company | Photocurable compositions |
| GB2514139A (en) | 2013-05-14 | 2014-11-19 | Aghababaie Lin & Co Ltd | Apparatus for fabrication of three dimensional objects |
| CN103342793B (zh) * | 2013-05-31 | 2015-08-05 | 成都彭州立源高分子材料有限公司 | 一种有机氟硅杂化光敏树脂及其合成方法 |
| US10513626B2 (en) | 2013-06-26 | 2019-12-24 | 3M Innovative Properties Company | Stain resistant microsphere articles |
| US10185058B2 (en) | 2013-07-01 | 2019-01-22 | 3M Innovative Properties Company | Protection film suitable for illuminated display devices |
| CN105899623B (zh) | 2014-01-15 | 2018-08-10 | 3M创新有限公司 | 包含烷氧基化的多(甲基)丙烯酸酯单体和经表面处理的纳米粒子的硬质涂膜 |
| CN106029736A (zh) * | 2014-02-19 | 2016-10-12 | 3M创新有限公司 | 混杂含氟弹性体组合物、可固化的组合物以及它们的制备和使用方法 |
| US9904001B2 (en) | 2014-03-18 | 2018-02-27 | 3M Innovative Properties Company | Marketing strip with viscoelastic lightguide |
| WO2015157329A1 (en) * | 2014-04-07 | 2015-10-15 | The Board Of Regents Of The University Of Texas System | Restorative resin compositions and methods of use |
| US10166725B2 (en) | 2014-09-08 | 2019-01-01 | Holo, Inc. | Three dimensional printing adhesion reduction using photoinhibition |
| WO2016069239A2 (en) | 2014-10-28 | 2016-05-06 | 3M Innovative Properties Company | Repellent coatings comprising sintered particles and lubricant, articles & method |
| RU2687436C2 (ru) | 2014-10-28 | 2019-05-13 | 3М Инновейтив Пропертиз Компани | Компоненты системы нанесения распылением с гидрофобной поверхностью и способы |
| WO2017074817A1 (en) | 2015-10-28 | 2017-05-04 | 3M Innovative Properties Company | Spray application system components comprising a repellent surface & methods |
| JP6619008B2 (ja) * | 2014-12-08 | 2019-12-11 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングBASF Coatings GmbH | コーティング材料組成物、およびそれらから生成されるコーティング、ならびにその使用方法 |
| EP3230062B1 (en) | 2014-12-08 | 2022-08-10 | 3M Innovative Properties Company | Acrylic polyvinyl acetal films |
| EP3230334B1 (de) * | 2014-12-08 | 2019-05-01 | BASF Coatings GmbH | Nichtwässrige beschichtungsmittelzusammensetzungen, daraus hergestellte beschichtungen mit verbesserter haftung und kratzfestigkeit sowie deren verwendung |
| AT516558B1 (de) * | 2014-12-10 | 2018-02-15 | Joanneum Res Forschungsgmbh | Prägelack, Verfahren zum Prägen sowie mit dem Prägelack beschichtete Substratoberfläche |
| CN107108667A (zh) | 2014-12-22 | 2017-08-29 | 3M创新有限公司 | 立体受阻胺和氧烷基胺光稳定剂 |
| WO2016105993A1 (en) | 2014-12-22 | 2016-06-30 | 3M Innovative Properties Company | Sterically hindered alkyl and oxyalkyl amine light stabilizers |
| EP3237426A1 (en) | 2014-12-22 | 2017-11-01 | 3M Innovative Properties Company | Sterically hindered amine and oxyalkyl amine light stabilizers |
| KR102551428B1 (ko) | 2015-03-18 | 2023-07-04 | 리껭테크노스 가부시키가이샤 | 다층 하드 코팅 필름 |
| PH12017501311B1 (en) | 2015-03-18 | 2024-07-03 | Riken Technos Corp | Hard coat laminate film and method for producing same |
| US11433651B2 (en) | 2015-03-18 | 2022-09-06 | Riken Technos Corporation | Hard coat laminated film |
| US10780685B2 (en) | 2015-03-18 | 2020-09-22 | Riken Technos Corporation | Hard coat laminated film |
| WO2016147716A1 (ja) | 2015-03-18 | 2016-09-22 | リケンテクノス株式会社 | 粘着フィルム |
| KR101970093B1 (ko) | 2015-03-18 | 2019-04-17 | 리껭테크노스 가부시키가이샤 | 방현성 하드 코트 적층 필름 |
| EP3663089B1 (en) | 2015-03-18 | 2024-07-10 | Riken Technos Corporation | Molded body |
| US9923245B2 (en) | 2015-04-03 | 2018-03-20 | Seeo, Inc. | Fluorinated alkali ion electrolytes with urethane groups |
| WO2016161465A1 (en) * | 2015-04-03 | 2016-10-06 | Seeo, Inc. | Fluorinated alkali ion electrolytes with urethane groups |
| WO2016164505A1 (en) | 2015-04-07 | 2016-10-13 | Seeo, Inc. | Fluorinated alkali ion electrolytes with cyclic carbonate groups |
| JP6547384B2 (ja) * | 2015-04-17 | 2019-07-24 | ダイキン工業株式会社 | 表面処理組成物 |
| WO2016172015A1 (en) * | 2015-04-20 | 2016-10-27 | 3M Innovative Properties Company | Durable low emissivity window film constructions |
| CN107531871A (zh) * | 2015-04-30 | 2018-01-02 | 旭硝子株式会社 | 含氟化合物、光固化性组合物、涂布液、硬质涂层形成用组合物以及物品 |
| KR20180005173A (ko) | 2015-05-12 | 2018-01-15 | 시오 인코퍼레이티드 | 리튬 배터리를 위한 전해질로서의 peo 및 플루오르화 중합체의 공중합체 |
| WO2016200559A1 (en) | 2015-06-09 | 2016-12-15 | Seeo, Inc. | Peo-based graft copolymers with pendant fluorinated groups for use as electrolytes |
| KR102543985B1 (ko) * | 2015-10-27 | 2023-06-14 | 삼성전자주식회사 | 전도막 및 이를 포함하는 전자 소자 |
| EP3368618B1 (en) | 2015-10-28 | 2020-11-25 | 3M Innovative Properties Company | Articles subject to ice formation comprising a repellent surface |
| US11774166B2 (en) | 2015-11-25 | 2023-10-03 | Riken Technos Corporation | Door body |
| TWI745316B (zh) | 2015-11-25 | 2021-11-11 | 日商理研科技股份有限公司 | 門體 |
| JP6644534B2 (ja) | 2015-12-08 | 2020-02-12 | リケンテクノス株式会社 | ハードコート積層フィルム |
| US11141919B2 (en) | 2015-12-09 | 2021-10-12 | Holo, Inc. | Multi-material stereolithographic three dimensional printing |
| WO2017112537A1 (en) | 2015-12-22 | 2017-06-29 | 3M Innovative Properties Company | Acrylic polyvinyl acetal films comprising an adhesive layer |
| EP3393795A2 (en) | 2015-12-22 | 2018-10-31 | 3M Innovative Properties Company | Acrylic films comprising a structured layer |
| CN108430769B (zh) | 2015-12-22 | 2021-07-16 | 3M创新有限公司 | 包括第二层的丙烯酸类聚乙烯醇缩醛膜 |
| WO2017112458A1 (en) | 2015-12-22 | 2017-06-29 | 3M Innovative Properties Company | Acrylic polyvinyl acetal graphic films |
| WO2017108510A1 (en) * | 2015-12-23 | 2017-06-29 | Solvay Specialty Polymers Italy S.P.A. | Method for coating printed circuit boards |
| CN105440170B (zh) * | 2016-01-29 | 2018-07-20 | 中远关西涂料(上海)有限公司 | 一种改性氟碳树脂及由其制备的无异氰酸酯氟碳树脂 |
| CN109071992A (zh) | 2016-04-26 | 2018-12-21 | 3M创新有限公司 | 包括包含硅氧烷材料的排斥性表面的经受冰形成的制品 |
| JP6872562B2 (ja) | 2016-05-10 | 2021-05-19 | シーオ インコーポレーテッドSeeo, Inc. | ニトリル基を有するフッ素化電解質 |
| EP3468795A2 (en) | 2016-06-09 | 2019-04-17 | 3M Innovative Properties Company | Polyurethane acrylate protective display film |
| JP2019529963A (ja) | 2016-07-01 | 2019-10-17 | スリーエム イノベイティブ プロパティズ カンパニー | 低Tgポリウレタン保護ディスプレイフィルム |
| CN109922959B (zh) | 2016-09-14 | 2021-01-12 | 理研科技株式会社 | 硬质涂层层压膜 |
| US10941313B2 (en) | 2016-11-21 | 2021-03-09 | 3M Innovative Properties Company | Flexible hardcoat comprising urethane oligomer hydrogen bonded to an acrylic polymer |
| JP7064313B2 (ja) | 2016-11-25 | 2022-05-10 | リケンテクノス株式会社 | ハードコート積層フィルム |
| US11631829B2 (en) | 2016-12-01 | 2023-04-18 | 3M Innovative Properties Company | Dual cure protective display film |
| TW201830102A (zh) | 2016-12-14 | 2018-08-16 | 美商3M新設資產公司 | 分段保護顯示膜 |
| US11065855B2 (en) | 2016-12-16 | 2021-07-20 | 3M Innovative Properties Company | Infrared-reflecting optically transparent assembly and method of making the same |
| US10935891B2 (en) | 2017-03-13 | 2021-03-02 | Holo, Inc. | Multi wavelength stereolithography hardware configurations |
| CN110461894B (zh) * | 2017-03-31 | 2022-09-02 | 大金工业株式会社 | 固化性组合物、其制造方法以及使用该固化性组合物的物品 |
| GB2564956B (en) | 2017-05-15 | 2020-04-29 | Holo Inc | Viscous film three-dimensional printing systems and methods |
| CN107286836A (zh) * | 2017-06-02 | 2017-10-24 | 广东北玻电子玻璃有限公司 | 一种抗眩光涂覆液及其制备方法 |
| US10245785B2 (en) | 2017-06-16 | 2019-04-02 | Holo, Inc. | Methods for stereolithography three-dimensional printing |
| KR102731347B1 (ko) | 2017-12-08 | 2024-11-15 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 가요성 하드코트 |
| WO2019116181A1 (en) | 2017-12-12 | 2019-06-20 | 3M Innovative Properties Company | Compositions including alpha-alumina particles and methods of their use |
| CN111465894A (zh) | 2017-12-13 | 2020-07-28 | 3M创新有限公司 | 高透射率光控膜 |
| EP3724704A4 (en) | 2017-12-13 | 2021-12-22 | 3M Innovative Properties Company | CONTROL FILM WITH HIGH LIGHT TRANSMISSION |
| CN111684022B (zh) | 2018-01-24 | 2023-04-11 | 3M创新有限公司 | 包含氢键合到适用于可拉伸膜的丙烯酸类聚合物的氨基甲酸酯低聚物的柔性硬质涂层 |
| JP2021514422A (ja) * | 2018-02-16 | 2021-06-10 | クラウン エレクトロキネティクス コーポレイション | 電気泳動ディスプレイ及び他の応用のための屈折率調和レジン |
| CN108559087B (zh) * | 2018-04-26 | 2021-05-25 | 太仓中化环保化工有限公司 | 一种具有uv光固化活性的防污防涂鸦助剂的制备方法 |
| CN112218753A (zh) | 2018-06-04 | 2021-01-12 | 3M创新有限公司 | 热成形耐磨多层光学膜及其制备方法 |
| EP3807369B1 (en) | 2018-06-12 | 2024-07-24 | 3M Innovative Properties Company | Fluoropolymer compositions comprising fluorinated additives, coated substrates and methods |
| EP3807344B1 (en) | 2018-06-12 | 2023-12-27 | 3M Innovative Properties Company | Fluoropolymer coating compositions comprising aminosilane curing agents, coated substrates and related methods |
| WO2020016708A2 (en) | 2018-07-18 | 2020-01-23 | 3M Innovative Properties Company | Vehicle sensors comprising repellent surface, protective films, repellent coating compositions, and methods |
| CN108912874B (zh) * | 2018-07-27 | 2020-12-29 | 江苏坦能纳米材料科技有限公司 | 一种高清投影漆及其制备方法和应用 |
| US11550183B2 (en) | 2018-08-01 | 2023-01-10 | 3M Innovative Properties Company | High transmission light control film |
| CN112534009A (zh) * | 2018-08-08 | 2021-03-19 | 三菱瓦斯化学株式会社 | 硬涂层组合物、叠层体膜和固化膜 |
| EP3659964A1 (en) * | 2018-11-28 | 2020-06-03 | Hysilabs, SAS | Catalysed process of production of hydrogen from silylated derivatives as hydrogen carrier compounds |
| CN113490867B (zh) | 2018-12-11 | 2025-02-21 | 3M创新有限公司 | 光控膜 |
| EP3902659A4 (en) | 2018-12-26 | 2022-09-07 | Holo, Inc. | SENSORS FOR THREE-DIMENSIONAL PRESSURE SYSTEMS AND PROCESSES |
| US12103846B2 (en) | 2019-05-08 | 2024-10-01 | 3M Innovative Properties Company | Nanostructured article |
| CN114072468A (zh) | 2019-05-09 | 2022-02-18 | 3M创新有限公司 | 柔性硬质涂层 |
| US11827802B2 (en) | 2019-05-09 | 2023-11-28 | 3M Innovative Properties Company | Flexible hardcoat |
| WO2020225703A1 (en) | 2019-05-09 | 2020-11-12 | 3M Innovative Properties Company | Flexible hardcoat |
| US12320993B2 (en) | 2019-06-12 | 2025-06-03 | 3M Innovative Properties Company | High transmission light control films with asymmetric light output |
| CN113994241A (zh) | 2019-06-12 | 2022-01-28 | 3M创新有限公司 | 包括导电粒子和有机聚合物的干燥含水分散体的涂覆基板 |
| MX2022003503A (es) | 2019-10-15 | 2022-04-25 | Akzo Nobel Coatings Int Bv | Composicion de recubrimiento curable por uv, a base de agua para recubrimientos faciles de limpiar. |
| WO2021088198A1 (en) | 2019-11-04 | 2021-05-14 | 3M Innovative Properties Company | Electronic telecommunications articles comprising crosslinked fluoropolymers and methods |
| CN114630874B (zh) | 2019-11-04 | 2023-12-05 | 3M创新有限公司 | 包含具有烯键式不饱和基团和电子供体基团的固化剂的含氟聚合物组合物及用其涂覆的基底 |
| CN114829986B (zh) | 2019-12-02 | 2025-05-16 | 3M创新有限公司 | 光学超表面膜 |
| CN114846369B (zh) | 2019-12-23 | 2024-10-25 | 3M创新有限公司 | 高透射率光控膜 |
| EP4143612A4 (en) | 2020-05-01 | 2024-05-08 | 3M Innovative Properties Company | REFLECTIVE OPTICAL METASURFACE FILMS |
| US12305063B2 (en) | 2020-05-14 | 2025-05-20 | 3M Innovative Properties Company | Fluorinated coupling agents and fluorinated (co)polymer layers made using the same |
| WO2021229331A1 (en) | 2020-05-14 | 2021-11-18 | 3M Innovative Properties Company | Compounds comprising perfluorinated group, photoinitiator group, and amide linking group |
| WO2021229340A1 (en) | 2020-05-14 | 2021-11-18 | 3M Innovative Properties Company | Fluorinated photoinitiators and fluorinated (co)polymer layers made using the same |
| EP4149752A4 (en) * | 2020-05-15 | 2024-05-29 | 3M Innovative Properties Company | MULTILAYER OPTICAL FILMS COMPRISING AT LEAST ONE LAYER OF FLUORINATED (CO)POLYMER PREPARED USING A FLUORINATED COUPLING AGENT, AND METHODS OF PREPARATION AND USE THEREOF |
| TWI897970B (zh) | 2020-06-11 | 2025-09-21 | 美商3M新設資產公司 | 包含全氟化基團、可水解矽烷基團、及(甲基)丙烯醯基之胺甲酸酯化合物 |
| CN116615331A (zh) | 2020-12-18 | 2023-08-18 | 3M创新有限公司 | 结构化膜和包括结构化膜的光学制品 |
| JP7486886B2 (ja) * | 2021-07-15 | 2024-05-20 | エルジー エナジー ソリューション リミテッド | 電解質組成物、ゲルポリマー電解質、およびそれを含むリチウム二次電池 |
| WO2023047204A1 (en) | 2021-09-24 | 2023-03-30 | 3M Innovative Properties Company | Coated microstructured films, methods of making same, and methods of making light control films |
| WO2023074410A1 (ja) * | 2021-10-28 | 2023-05-04 | ダイキン工業株式会社 | 表面処理剤 |
| EP4445188A1 (en) | 2021-12-09 | 2024-10-16 | 3M Innovative Properties Company | Coated microstructured films and methods of making same |
| WO2023190742A1 (ja) * | 2022-03-31 | 2023-10-05 | ダイキン工業株式会社 | 硬化性組成物 |
| JP7723287B2 (ja) * | 2022-03-31 | 2025-08-14 | ダイキン工業株式会社 | 硬化性組成物 |
| JP7644378B2 (ja) * | 2022-03-31 | 2025-03-12 | ダイキン工業株式会社 | 硬化性組成物 |
| JP7644377B2 (ja) * | 2022-03-31 | 2025-03-12 | ダイキン工業株式会社 | 硬化性組成物 |
| CN117467337B (zh) * | 2023-12-25 | 2024-03-12 | 成都虹润制漆有限公司 | 一种钢结构用的重防腐涂料配套体系及其制备方法 |
Family Cites Families (102)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3250808A (en) * | 1963-10-31 | 1966-05-10 | Du Pont | Fluorocarbon ethers derived from hexafluoropropylene epoxide |
| US4085137A (en) * | 1969-03-10 | 1978-04-18 | Minnesota Mining And Manufacturing Company | Poly(perfluoroalkylene oxide) derivatives |
| DE2024909B2 (de) * | 1970-05-22 | 1977-09-29 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von n-hydroxyalkyl-perfluoralkansulfonamiden und einige n,n-bis-(hydroxyalkyl)-perfluor-alkansulfonamide |
| US4262072A (en) * | 1979-06-25 | 1981-04-14 | Minnesota Mining And Manufacturing Company | Poly(ethylenically unsaturated alkoxy) heterocyclic protective coatings |
| US4321404A (en) * | 1980-05-20 | 1982-03-23 | Minnesota Mining And Manufacturing Company | Compositions for providing abherent coatings |
| US4818801A (en) | 1982-01-18 | 1989-04-04 | Minnesota Mining And Manufacturing Company | Ophthalmic device comprising a polymer of a telechelic perfluoropolyether |
| US4472480A (en) * | 1982-07-02 | 1984-09-18 | Minnesota Mining And Manufacturing Company | Low surface energy liner of perfluoropolyether |
| US4614667A (en) * | 1984-05-21 | 1986-09-30 | Minnesota Mining And Manufacturing Company | Composite low surface energy liner of perfluoropolyether |
| US4654233A (en) * | 1984-11-21 | 1987-03-31 | Minnesota Mining And Manufacturing Company | Radiation-curable thermoplastic coating |
| FR2590895B1 (fr) * | 1985-12-03 | 1988-01-15 | Atochem | Monomeres acryliques fluores, polymeres en derivant et leur application comme agents hydrophobes et oleophobes |
| US4825249A (en) | 1987-03-14 | 1989-04-25 | Ntn-Rulon Industries Co., Ltd. | Cleaning blade for use with photoelectronic copying machine |
| US4855184A (en) * | 1988-02-02 | 1989-08-08 | Minnesota Mining And Manufacturing Company | Radiation-curable protective coating composition |
| AU608420B2 (en) * | 1988-03-15 | 1991-03-28 | Minnesota Mining And Manufacturing Company | Polymer claddings for optical fibre waveguides |
| US4873140A (en) | 1988-04-27 | 1989-10-10 | Minnesota Mining And Manufacturing Company | Articles having low adhesion articles having coatings thereon |
| ATE118797T1 (de) | 1989-01-11 | 1995-03-15 | Ciba Geigy Ag | Perfluorpolyalkylether- und polyalkylether- segmente enthaltende vinylmakromere, daraus hergestellte polymere, interpolymere sowie ophthalmische vorrichtungen. |
| US4929692A (en) * | 1989-01-11 | 1990-05-29 | Ciba-Geigy Corporation | Crosslinked copolymers and ophthalmic devices made from vinylic macromers containing perfluoropolyalkyl ether and polyalkyl ether segments and minor amounts of vinylic comonomers |
| AU632869B2 (en) | 1989-12-14 | 1993-01-14 | Minnesota Mining And Manufacturing Company | Fluorocarbon-based coating compositions and articles derived therefrom |
| IT1253002B (it) | 1990-10-05 | 1995-07-10 | Minnesota Mining & Mfg | Elemento fotografico agli alogenuri d'argento e procedimento per preparare una dispersione in composizioni acquose di particelle discrete di un agente mattante polimerico insolubile in acqua |
| EP0539585A4 (en) | 1991-04-22 | 1993-09-01 | Takata Corporation | Surface-coated member |
| DE4113634A1 (de) * | 1991-04-26 | 1992-10-29 | Minnesota Mining & Mfg | Fluoracryl-polymere, verfahren zu ihrer herstellung und ihre anwendung |
| US5239026A (en) * | 1991-08-26 | 1993-08-24 | Minnesota Mining And Manufacturing Company | Low loss high numerical aperture cladded optical fibers |
| US5148511A (en) * | 1991-11-04 | 1992-09-15 | Minnesota Mining And Manufacturing Company | Low refractive index plastics for optical fiber cladding |
| JP3161552B2 (ja) | 1992-01-31 | 2001-04-25 | 大日本インキ化学工業株式会社 | 硬化性組成物及び絶縁電線 |
| WO1995018194A1 (en) | 1993-12-29 | 1995-07-06 | Daikin Industries, Ltd. | Fluorinated oil/water emulsion and surface treatment composition |
| JPH11503768A (ja) | 1995-01-30 | 1999-03-30 | デー エス エム エヌ.ヴェー. | フッ素化ウレタンオリゴマー含有放射線硬化性組成物 |
| US5609990A (en) * | 1995-02-08 | 1997-03-11 | Imation Corp. | Optical recording disk having a sealcoat layer |
| AUPN215995A0 (en) * | 1995-04-04 | 1995-04-27 | Ciba-Geigy Ag | Novel materials |
| IT1273609B (it) * | 1995-04-28 | 1997-07-08 | Ausimont Spa | Procedimento per la protezione delle superfici lapidee o di rivestimento |
| US5677050A (en) * | 1995-05-19 | 1997-10-14 | Minnesota Mining And Manufacturing Company | Retroreflective sheeting having an abrasion resistant ceramer coating |
| US5846650A (en) * | 1996-05-10 | 1998-12-08 | Minnesota Mining And Manufacturing Company | Anti-reflective, abrasion resistant, anti-fogging coated articles and methods |
| JPH10110118A (ja) | 1996-08-13 | 1998-04-28 | Toray Ind Inc | 防汚性ハードコート剤および光記録媒体 |
| US5822489A (en) * | 1996-12-31 | 1998-10-13 | Lucent Technologies, Inc. | Low refractive index photo-curable composition for waveguide applications |
| US6210858B1 (en) | 1997-04-04 | 2001-04-03 | Fuji Photo Film Co., Ltd. | Anti-reflection film and display device using the same |
| IT1290462B1 (it) * | 1997-04-08 | 1998-12-03 | Ausimont Spa | Polimeri idrogenati modificati |
| JP4267088B2 (ja) | 1997-09-05 | 2009-05-27 | パナソニック株式会社 | 反射防止膜用塗料及び該反射防止膜用塗料を用いた低反射材 |
| JPH11213444A (ja) | 1998-01-30 | 1999-08-06 | Sony Corp | 光記録媒体 |
| US7351470B2 (en) * | 1998-02-19 | 2008-04-01 | 3M Innovative Properties Company | Removable antireflection film |
| US6800378B2 (en) | 1998-02-19 | 2004-10-05 | 3M Innovative Properties Company | Antireflection films for use with displays |
| JPH11293159A (ja) | 1998-04-09 | 1999-10-26 | Toray Ind Inc | 光記録媒体用ハードコート剤および光記録媒体 |
| US6224949B1 (en) * | 1998-06-11 | 2001-05-01 | 3M Innovative Properties Company | Free radical polymerization method |
| US6238798B1 (en) * | 1999-02-22 | 2001-05-29 | 3M Innovative Properties Company | Ceramer composition and composite comprising free radically curable fluorochemical component |
| US6299799B1 (en) | 1999-05-27 | 2001-10-09 | 3M Innovative Properties Company | Ceramer compositions and antistatic abrasion resistant ceramers made therefrom |
| IT1312344B1 (it) | 1999-06-03 | 2002-04-15 | Ausimont Spa | Composizioni per film a basso indice di rifrazione. |
| US6673889B1 (en) | 1999-06-28 | 2004-01-06 | Omnova Solutions Inc. | Radiation curable coating containing polyfuorooxetane |
| JP4855616B2 (ja) | 1999-10-27 | 2012-01-18 | スリーエム イノベイティブ プロパティズ カンパニー | フルオロケミカルスルホンアミド界面活性剤 |
| JP4590758B2 (ja) | 2000-04-10 | 2010-12-01 | Tdk株式会社 | 光情報媒体 |
| JP5004065B2 (ja) | 2000-05-19 | 2012-08-22 | 東レフィルム加工株式会社 | 積層フィルムおよびその製造方法 |
| JP2002003595A (ja) | 2000-06-22 | 2002-01-09 | Shin Etsu Chem Co Ltd | 含フッ素硬化物 |
| JP4782934B2 (ja) | 2000-09-27 | 2011-09-28 | 日本化薬株式会社 | 低屈折率樹脂組成物およびその硬化物 |
| AU2002249787A1 (en) * | 2000-10-25 | 2002-08-19 | Diadexus, Inc. | Compositions and methods relating to lung specific genes and proteins |
| US6632508B1 (en) * | 2000-10-27 | 2003-10-14 | 3M Innovative Properties Company | Optical elements comprising a polyfluoropolyether surface treatment |
| JP2002202402A (ja) * | 2000-10-31 | 2002-07-19 | Fuji Photo Film Co Ltd | 防眩性反射防止フィルムおよび画像表示装置 |
| US7351471B2 (en) | 2000-12-06 | 2008-04-01 | 3M Innovative Properties Company | Fluoropolymer coating compositions with multifunctional fluoroalkyl crosslinkers for anti-reflective polymer films |
| US20020115820A1 (en) * | 2001-01-25 | 2002-08-22 | Fang Wang | Hyperbranched fluorinated multifunctional alcohols and derivatives |
| US6689900B2 (en) * | 2001-02-09 | 2004-02-10 | E. I. Du Pont De Nemours And Company | Fluorinated crosslinker and composition |
| JP3923340B2 (ja) | 2001-03-05 | 2007-05-30 | 共栄社化学株式会社 | パーフルオロアルキル基含有プレポリマーおよびその重合硬化物 |
| US6660338B1 (en) * | 2001-03-08 | 2003-12-09 | Agilent Technologies, Inc. | Functionalization of substrate surfaces with silane mixtures |
| US6676572B2 (en) * | 2001-04-06 | 2004-01-13 | Leao Wang | Folding mechanism of an exercise treadmill |
| EP1411073B1 (en) | 2001-06-27 | 2013-03-20 | Daikin Industries, Ltd. | Surface-treating agent composition and process for producing the same |
| WO2003009904A1 (en) | 2001-07-24 | 2003-02-06 | Zenjiro Shiotsu | Ball manufacturing method |
| ATE377503T1 (de) * | 2001-12-26 | 2007-11-15 | Tdk Corp | Artikel mit harter verbundbeschichtungsschicht und verfahren zur herstellung der harten verbundbeschichtungsschicht |
| TWI229115B (en) | 2002-02-11 | 2005-03-11 | Sipix Imaging Inc | Core-shell particles for electrophoretic display |
| US6582759B1 (en) | 2002-02-15 | 2003-06-24 | 3M Innovative Properties Company | Optical elements comprising a fluorinated surface treatment comprising urethane, ester or phosphate linkages |
| KR100487025B1 (ko) | 2002-02-28 | 2005-05-11 | 주식회사 루밴틱스 | 광도파로용 광경화성 수지 조성물 및 이로부터 제조된광도파로 |
| BR0311256A (pt) * | 2002-05-24 | 2005-03-15 | 3M Innovative Properties Co | Composição fluoroquìmica, método de tratamento, monÈmero de poliéter fluorado, e, homo- ou copolìmero fluorado |
| WO2003102500A1 (en) * | 2002-06-04 | 2003-12-11 | Olympus Corporation | Method of obtaining 3-d coordinates |
| JP3732840B2 (ja) | 2002-06-27 | 2006-01-11 | Tdk株式会社 | 複合ハードコート層付き物体及び複合ハードコート層の形成方法 |
| CN100408326C (zh) * | 2002-06-27 | 2008-08-06 | Tdk株式会社 | 带有复合硬涂层的物体及复合硬涂层的形成方法 |
| JP2004043671A (ja) | 2002-07-12 | 2004-02-12 | Nippon Kayaku Co Ltd | 低屈折率樹脂組成物およびその硬化物 |
| EP2219051A1 (en) | 2002-08-15 | 2010-08-18 | Fujifilm Corporation | Antireflection film, polarizing plate and image display device |
| KR101014582B1 (ko) * | 2002-11-13 | 2011-02-16 | 아사히 가라스 가부시키가이샤 | 활성 에너지선 경화형 피복용 조성물 및 그 조성물의경화물로 이루어지는 피막을 갖는 성형품 |
| JP4886152B2 (ja) | 2002-12-26 | 2012-02-29 | 日本合成化学工業株式会社 | ウレタン(メタ)アクリレート系化合物及びそれを用いた活性エネルギー線硬化型樹脂組成物 |
| KR101067534B1 (ko) * | 2003-03-31 | 2011-09-27 | 린텍 가부시키가이샤 | 광학용 필름 |
| JP4126545B2 (ja) | 2003-04-18 | 2008-07-30 | 信越化学工業株式会社 | 被覆物品並びに多層積層体 |
| JP4248347B2 (ja) | 2003-09-03 | 2009-04-02 | 富士フイルム株式会社 | 皮膜形成用組成物、反射防止膜、偏光板、画像表示装置及び防汚性コーティング組成物及び防汚性物品 |
| JP4590849B2 (ja) * | 2003-10-03 | 2010-12-01 | Tdk株式会社 | ハードコート剤組成物及びこれを用いた光情報媒体 |
| JP4779293B2 (ja) * | 2003-10-21 | 2011-09-28 | Tdk株式会社 | ハードコート剤組成物及びこれを用いた光情報媒体 |
| JP4319522B2 (ja) * | 2003-10-31 | 2009-08-26 | Tdk株式会社 | 光情報媒体 |
| US6998425B2 (en) * | 2003-12-23 | 2006-02-14 | General Electric Company | UV curable coating compositions and uses thereof |
| JP4784723B2 (ja) * | 2003-12-24 | 2011-10-05 | Tdk株式会社 | ハードコート剤組成物及びこれを用いた光情報媒体 |
| TWI388876B (zh) | 2003-12-26 | 2013-03-11 | Fujifilm Corp | 抗反射膜、偏光板,其製造方法,液晶顯示元件,液晶顯示裝置,及影像顯示裝置 |
| US20050228152A1 (en) | 2004-04-08 | 2005-10-13 | Starry Adam B | Anti-reflective coating |
| JP2007535590A (ja) | 2004-04-22 | 2007-12-06 | Jsr株式会社 | 低屈折率コーティング組成物 |
| US20050249956A1 (en) | 2004-05-07 | 2005-11-10 | Naiyong Jing | Stain repellent optical hard coating |
| US20050249940A1 (en) | 2004-05-07 | 2005-11-10 | 3M Innovative Properties Company | Fluoropolyether poly(meth)acryl compounds |
| EP1758959A1 (en) | 2004-05-07 | 2007-03-07 | 3M Innovative Properties Company | Stain repellent optical hard coating |
| US20070183997A9 (en) * | 2004-06-08 | 2007-08-09 | Lebre Caroline | Composition comprising particles of at least one polymer dispersed in at least one fatty phase and at least one apolar oil |
| JP2006037024A (ja) | 2004-07-29 | 2006-02-09 | Daikin Ind Ltd | 反射防止膜形成用組成物 |
| US20060105155A1 (en) | 2004-11-16 | 2006-05-18 | Fuji Photo Film Co., Ltd. | Optical film, polarizing plate and method for forming optical film |
| US20060148996A1 (en) * | 2004-12-30 | 2006-07-06 | Coggio William D | Low refractive index fluoropolymer compositions having improved coating and durability properties |
| US20060216524A1 (en) * | 2005-03-23 | 2006-09-28 | 3M Innovative Properties Company | Perfluoropolyether urethane additives having (meth)acryl groups and hard coats |
| US7615283B2 (en) | 2006-06-13 | 2009-11-10 | 3M Innovative Properties Company | Fluoro(meth)acrylate polymer composition suitable for low index layer of antireflective film |
| US7537828B2 (en) * | 2006-06-13 | 2009-05-26 | 3M Innovative Properties Company | Low refractive index composition comprising fluoropolyether urethane compound |
| US7575847B2 (en) * | 2006-06-13 | 2009-08-18 | 3M Innovative Properties Company | Low refractive index composition comprising fluoropolyether urethane compound |
| US20070292679A1 (en) * | 2006-06-14 | 2007-12-20 | 3M Innovative Properties Company | Optical article having an antistatic fluorochemical surface layer |
| US8530054B2 (en) * | 2006-09-27 | 2013-09-10 | 3M Innovative Properties Company | Solar control multilayer film |
| US20080124555A1 (en) * | 2006-11-29 | 2008-05-29 | 3M Innovative Properties Company | Polymerizable composition comprising perfluoropolyether urethane having ethylene oxide repeat units |
| US8015970B2 (en) * | 2007-07-26 | 2011-09-13 | 3M Innovative Properties Company | Respirator, welding helmet, or face shield that has low surface energy hard-coat lens |
| WO2009029438A1 (en) * | 2007-08-31 | 2009-03-05 | 3M Innovative Properties Company | Hardcoats |
| JP5209030B2 (ja) | 2010-11-11 | 2013-06-12 | ▲がい▼笛森光電股▲ふん▼有限公司 | 相異発光素子を有する傾斜検出器及びその操作方法 |
| US8742022B2 (en) * | 2010-12-20 | 2014-06-03 | 3M Innovative Properties Company | Coating compositions comprising non-ionic surfactant exhibiting reduced fingerprint visibility |
| US8715904B2 (en) * | 2012-04-27 | 2014-05-06 | 3M Innovative Properties Company | Photocurable composition |
-
2005
- 2005-03-23 US US11/087,413 patent/US20060216524A1/en not_active Abandoned
-
2006
- 2006-03-22 TW TW95109966A patent/TWI412779B/zh not_active IP Right Cessation
- 2006-03-22 WO PCT/US2006/010344 patent/WO2006102383A1/en not_active Ceased
- 2006-03-22 KR KR1020077021774A patent/KR20070114190A/ko not_active Ceased
- 2006-03-22 US US11/277,162 patent/US7718264B2/en active Active
- 2006-03-22 CN CN2006800092064A patent/CN101146840B/zh not_active Expired - Fee Related
- 2006-03-22 EP EP06739223.3A patent/EP1866355B1/en not_active Not-in-force
- 2006-03-22 KR KR1020137013814A patent/KR101397831B1/ko not_active Expired - Fee Related
- 2006-03-22 JP JP2008503117A patent/JP5118017B2/ja not_active Expired - Fee Related
-
2010
- 2010-03-05 US US12/718,481 patent/US8147966B2/en not_active Expired - Lifetime
-
2012
- 2012-02-15 US US13/396,669 patent/US8476398B2/en not_active Expired - Lifetime
-
2013
- 2013-06-03 US US13/908,102 patent/US8729211B2/en not_active Expired - Fee Related
-
2014
- 2014-04-08 US US14/247,379 patent/US8981151B2/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9292259B2 (en) | 2008-08-06 | 2016-03-22 | Cassy Holdings Llc | Uncertainty random value generator |
| US9207911B2 (en) | 2009-07-31 | 2015-12-08 | Cassy Holdings Llc | Modular uncertainty random value generator and method |
| US11537362B2 (en) | 2009-07-31 | 2022-12-27 | Cassy Holdings Llc | Modular uncertainty random value generator and method |
| US9990180B2 (en) | 2011-05-27 | 2018-06-05 | Cassy Holdings Llc | Stochastic processing |
| KR20160108716A (ko) * | 2015-03-05 | 2016-09-20 | (주)엘지하우시스 | 인덱스매칭 필름 |
Also Published As
| Publication number | Publication date |
|---|---|
| US8981151B2 (en) | 2015-03-17 |
| CN101146840A (zh) | 2008-03-19 |
| US8476398B2 (en) | 2013-07-02 |
| US20140221689A1 (en) | 2014-08-07 |
| US20060216524A1 (en) | 2006-09-28 |
| CN101146840B (zh) | 2011-06-15 |
| JP2008538195A (ja) | 2008-10-16 |
| KR20130063551A (ko) | 2013-06-14 |
| US8729211B2 (en) | 2014-05-20 |
| US7718264B2 (en) | 2010-05-18 |
| WO2006102383A1 (en) | 2006-09-28 |
| US20120142883A1 (en) | 2012-06-07 |
| US20130261280A1 (en) | 2013-10-03 |
| KR101397831B1 (ko) | 2014-05-20 |
| TW200639422A (en) | 2006-11-16 |
| US20060216500A1 (en) | 2006-09-28 |
| US8147966B2 (en) | 2012-04-03 |
| JP5118017B2 (ja) | 2013-01-16 |
| US20100160595A1 (en) | 2010-06-24 |
| EP1866355A1 (en) | 2007-12-19 |
| TWI412779B (zh) | 2013-10-21 |
| EP1866355B1 (en) | 2017-08-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101397831B1 (ko) | (메트)아크릴 기 함유 퍼플루오로폴리에테르 우레탄 첨가제 및 하드코트 | |
| KR101455421B1 (ko) | 에틸렌 옥사이드 반복 단위 세그먼트를 가진 퍼플루오로폴리에테르 물질을 포함하는 중합성 조성물 | |
| JP4755178B2 (ja) | 防汚染性光学ハードコーティング | |
| EP2222752B1 (en) | Hardcoats comprising perfluoropolyether polymers with poly(alkylene oxide) repeat units | |
| US8728623B2 (en) | Hardcoats having low surface energy and low lint attraction | |
| US20070292679A1 (en) | Optical article having an antistatic fluorochemical surface layer | |
| WO2008039683A1 (en) | Solar control multilayer film | |
| US20080075951A1 (en) | Fluoroacrylates and hardcoat compositions including the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20070921 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20110321 Comment text: Request for Examination of Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20120917 Patent event code: PE09021S01D |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 20130327 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20120917 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |
|
| J201 | Request for trial against refusal decision | ||
| PJ0201 | Trial against decision of rejection |
Patent event date: 20130429 Comment text: Request for Trial against Decision on Refusal Patent event code: PJ02012R01D Patent event date: 20130327 Comment text: Decision to Refuse Application Patent event code: PJ02011S01I Appeal kind category: Appeal against decision to decline refusal Decision date: 20130624 Appeal identifier: 2013101003186 Request date: 20130429 |
|
| A107 | Divisional application of patent | ||
| PA0104 | Divisional application for international application |
Comment text: Divisional Application for International Patent Patent event code: PA01041R01D Patent event date: 20130529 |
|
| J121 | Written withdrawal of request for trial | ||
| PC1202 | Submission of document of withdrawal before decision of registration |
Comment text: [Withdrawal of Procedure relating to Patent, etc.] Withdrawal (Abandonment) Patent event code: PC12021R01D Patent event date: 20130624 |
|
| PJ1201 | Withdrawal of trial |
Patent event code: PJ12011R01D Patent event date: 20130624 Comment text: Written Withdrawal of Request for Trial Appeal identifier: 2013101003186 Request date: 20130429 Appeal kind category: Appeal against decision to decline refusal Decision date: 20130624 |
|
| WITB | Written withdrawal of application |