JP7499187B2 - 半導体金属酸化物材料を含む化学線硬化性組成物 - Google Patents
半導体金属酸化物材料を含む化学線硬化性組成物 Download PDFInfo
- Publication number
- JP7499187B2 JP7499187B2 JP2020561889A JP2020561889A JP7499187B2 JP 7499187 B2 JP7499187 B2 JP 7499187B2 JP 2020561889 A JP2020561889 A JP 2020561889A JP 2020561889 A JP2020561889 A JP 2020561889A JP 7499187 B2 JP7499187 B2 JP 7499187B2
- Authority
- JP
- Japan
- Prior art keywords
- composition
- metal oxide
- semiconducting
- red
- pigment
- 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.)
- Active
Links
- 229910044991 metal oxide Inorganic materials 0.000 title claims description 141
- 150000004706 metal oxides Chemical class 0.000 title claims description 131
- 239000000463 material Substances 0.000 title claims description 127
- 239000000203 mixture Substances 0.000 title claims description 127
- 230000005855 radiation Effects 0.000 title claims description 77
- 239000004065 semiconductor Substances 0.000 title description 40
- 239000002131 composite material Substances 0.000 claims description 81
- 239000000049 pigment Substances 0.000 claims description 51
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 40
- -1 aliphatic urethane acrylates Chemical class 0.000 claims description 39
- 239000000178 monomer Substances 0.000 claims description 29
- 238000010894 electron beam technology Methods 0.000 claims description 20
- 239000006229 carbon black Substances 0.000 claims description 19
- 239000000758 substrate Substances 0.000 claims description 16
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 15
- 230000001699 photocatalysis Effects 0.000 claims description 15
- 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 claims description 14
- 239000004927 clay Substances 0.000 claims description 11
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 10
- WMWLMWRWZQELOS-UHFFFAOYSA-N bismuth(iii) oxide Chemical compound O=[Bi]O[Bi]=O WMWLMWRWZQELOS-UHFFFAOYSA-N 0.000 claims description 10
- 238000010526 radical polymerization reaction Methods 0.000 claims description 10
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 9
- 239000004021 humic acid Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 8
- 239000000975 dye Substances 0.000 claims description 8
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 8
- 229910052753 mercury Inorganic materials 0.000 claims description 8
- QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 claims description 7
- 230000037361 pathway Effects 0.000 claims description 7
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 6
- 238000007639 printing Methods 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 230000000977 initiatory effect Effects 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 claims description 4
- 230000001070 adhesive effect Effects 0.000 claims description 4
- 229910001507 metal halide Inorganic materials 0.000 claims description 4
- 150000005309 metal halides Chemical class 0.000 claims description 4
- BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 claims description 4
- 238000004806 packaging method and process Methods 0.000 claims description 4
- 229920000570 polyether Polymers 0.000 claims description 4
- 229910052724 xenon Inorganic materials 0.000 claims description 4
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 claims description 4
- SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 3
- 229910052797 bismuth Inorganic materials 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 239000003921 oil Substances 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 150000004291 polyenes Chemical class 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- NDDLLTAIKYHPOD-ISLYRVAYSA-N (2e)-6-chloro-2-(6-chloro-4-methyl-3-oxo-1-benzothiophen-2-ylidene)-4-methyl-1-benzothiophen-3-one Chemical compound S/1C2=CC(Cl)=CC(C)=C2C(=O)C\1=C1/SC(C=C(Cl)C=C2C)=C2C1=O NDDLLTAIKYHPOD-ISLYRVAYSA-N 0.000 claims description 2
- XLTMWFMRJZDFFD-UHFFFAOYSA-N 1-[(2-chloro-4-nitrophenyl)diazenyl]naphthalen-2-ol Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=C([N+]([O-])=O)C=C1Cl XLTMWFMRJZDFFD-UHFFFAOYSA-N 0.000 claims description 2
- PWUSHZPXYOALFZ-UHFFFAOYSA-N 3-hydroxy-4-[(1-sulfonaphthalen-2-yl)diazenyl]naphthalene-2-carboxylic acid Chemical compound OC(=O)c1cc2ccccc2c(N=Nc2ccc3ccccc3c2S(O)(=O)=O)c1O PWUSHZPXYOALFZ-UHFFFAOYSA-N 0.000 claims description 2
- ZDTNHRWWURISAA-UHFFFAOYSA-N 4',5'-dibromo-3',6'-dihydroxyspiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C(Br)=C1OC1=C(Br)C(O)=CC=C21 ZDTNHRWWURISAA-UHFFFAOYSA-N 0.000 claims description 2
- WLDHEUZGFKACJH-ZRUFZDNISA-K Amaranth Chemical compound [Na+].[Na+].[Na+].C12=CC=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(O)=C1\N=N\C1=CC=C(S([O-])(=O)=O)C2=CC=CC=C12 WLDHEUZGFKACJH-ZRUFZDNISA-K 0.000 claims description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 2
- 239000001000 anthraquinone dye Substances 0.000 claims description 2
- ILZWGESBVHGTRX-UHFFFAOYSA-O azanium;iron(2+);iron(3+);hexacyanide Chemical compound [NH4+].[Fe+2].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] ILZWGESBVHGTRX-UHFFFAOYSA-O 0.000 claims description 2
- 239000000987 azo dye Substances 0.000 claims description 2
- 235000012745 brilliant blue FCF Nutrition 0.000 claims description 2
- 239000004161 brilliant blue FCF Substances 0.000 claims description 2
- DBZJJPROPLPMSN-UHFFFAOYSA-N bromoeosin Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(Br)=C(O)C(Br)=C1OC1=C(Br)C(O)=C(Br)C=C21 DBZJJPROPLPMSN-UHFFFAOYSA-N 0.000 claims description 2
- OIQPTROHQCGFEF-UHFFFAOYSA-L chembl1371409 Chemical compound [Na+].[Na+].OC1=CC=C2C=C(S([O-])(=O)=O)C=CC2=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 OIQPTROHQCGFEF-UHFFFAOYSA-L 0.000 claims description 2
- CEZCCHQBSQPRMU-UHFFFAOYSA-L chembl174821 Chemical compound [Na+].[Na+].COC1=CC(S([O-])(=O)=O)=C(C)C=C1N=NC1=C(O)C=CC2=CC(S([O-])(=O)=O)=CC=C12 CEZCCHQBSQPRMU-UHFFFAOYSA-L 0.000 claims description 2
- PZTQVMXMKVTIRC-UHFFFAOYSA-L chembl2028348 Chemical compound [Ca+2].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 PZTQVMXMKVTIRC-UHFFFAOYSA-L 0.000 claims description 2
- 229910000423 chromium oxide Inorganic materials 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 229940075479 d & c red no. 27 Drugs 0.000 claims description 2
- 229940090962 d&c orange no. 5 Drugs 0.000 claims description 2
- 229940058010 d&c red no. 21 Drugs 0.000 claims description 2
- 229940075484 d&c red no. 30 Drugs 0.000 claims description 2
- 229940047180 d&c red no. 34 Drugs 0.000 claims description 2
- 229940075493 d&c red no. 6 Drugs 0.000 claims description 2
- 229940057946 d&c red no. 7 Drugs 0.000 claims description 2
- VPWFPZBFBFHIIL-UHFFFAOYSA-L disodium 4-[(4-methyl-2-sulfophenyl)diazenyl]-3-oxidonaphthalene-2-carboxylate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 VPWFPZBFBFHIIL-UHFFFAOYSA-L 0.000 claims description 2
- LQJVOKWHGUAUHK-UHFFFAOYSA-L disodium 5-amino-4-hydroxy-3-phenyldiazenylnaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].OC1=C2C(N)=CC(S([O-])(=O)=O)=CC2=CC(S([O-])(=O)=O)=C1N=NC1=CC=CC=C1 LQJVOKWHGUAUHK-UHFFFAOYSA-L 0.000 claims description 2
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 claims description 2
- 229940057841 eosine yellowish Drugs 0.000 claims description 2
- 229940051147 fd&c yellow no. 6 Drugs 0.000 claims description 2
- 239000007850 fluorescent dye Substances 0.000 claims description 2
- 235000010187 litholrubine BK Nutrition 0.000 claims description 2
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 claims description 2
- ZYIBVBKZZZDFOY-UHFFFAOYSA-N phloxine O Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(Br)=C(O)C(Br)=C1OC1=C(Br)C(O)=C(Br)C=C21 ZYIBVBKZZZDFOY-UHFFFAOYSA-N 0.000 claims description 2
- 229940051201 quinoline yellow Drugs 0.000 claims description 2
- 235000012752 quinoline yellow Nutrition 0.000 claims description 2
- FZUOVNMHEAPVBW-UHFFFAOYSA-L quinoline yellow ws Chemical compound [Na+].[Na+].O=C1C2=CC=CC=C2C(=O)C1C1=NC2=C(S([O-])(=O)=O)C=C(S(=O)(=O)[O-])C=C2C=C1 FZUOVNMHEAPVBW-UHFFFAOYSA-L 0.000 claims description 2
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 claims description 2
- 239000001018 xanthene dye Substances 0.000 claims description 2
- 239000011111 cardboard Substances 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims 1
- 239000000123 paper Substances 0.000 claims 1
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 1
- 239000000976 ink Substances 0.000 description 71
- 238000001723 curing Methods 0.000 description 34
- 239000001993 wax Substances 0.000 description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 14
- 230000002829 reductive effect Effects 0.000 description 14
- 239000000654 additive Substances 0.000 description 12
- 230000003287 optical effect Effects 0.000 description 12
- 239000004743 Polypropylene Substances 0.000 description 10
- 230000001965 increasing effect Effects 0.000 description 10
- 229920001155 polypropylene Polymers 0.000 description 10
- 150000003254 radicals Chemical class 0.000 description 10
- 230000009467 reduction Effects 0.000 description 10
- 238000005259 measurement Methods 0.000 description 9
- 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 8
- 230000006872 improvement Effects 0.000 description 8
- 231100000331 toxic Toxicity 0.000 description 8
- 230000002588 toxic effect Effects 0.000 description 8
- 239000011787 zinc oxide Substances 0.000 description 8
- 230000008901 benefit Effects 0.000 description 7
- 239000003086 colorant Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 239000008199 coating composition Substances 0.000 description 6
- 235000013305 food Nutrition 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- ZDHCZVWCTKTBRY-UHFFFAOYSA-N omega-Hydroxydodecanoic acid Natural products OCCCCCCCCCCCC(O)=O ZDHCZVWCTKTBRY-UHFFFAOYSA-N 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 5
- 230000009977 dual effect Effects 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- PJAKWOZHTFWTNF-UHFFFAOYSA-N (2-nonylphenyl) prop-2-enoate Chemical compound CCCCCCCCCC1=CC=CC=C1OC(=O)C=C PJAKWOZHTFWTNF-UHFFFAOYSA-N 0.000 description 4
- 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 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 238000003848 UV Light-Curing Methods 0.000 description 4
- 125000004386 diacrylate group Chemical group 0.000 description 4
- 238000000113 differential scanning calorimetry Methods 0.000 description 4
- 230000005284 excitation Effects 0.000 description 4
- 239000001023 inorganic pigment Substances 0.000 description 4
- 238000001459 lithography Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000011941 photocatalyst Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 3
- 229920002799 BoPET Polymers 0.000 description 3
- 239000004970 Chain extender Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- FHLPGTXWCFQMIU-UHFFFAOYSA-N [4-[2-(4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical class 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 3
- 238000010521 absorption reaction Methods 0.000 description 3
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 description 3
- 238000007774 anilox coating Methods 0.000 description 3
- 230000005670 electromagnetic radiation Effects 0.000 description 3
- 239000003623 enhancer Substances 0.000 description 3
- 230000002708 enhancing effect Effects 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 229910052621 halloysite Inorganic materials 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000012860 organic pigment Substances 0.000 description 3
- 239000005026 oriented polypropylene Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910001868 water Inorganic materials 0.000 description 3
- 230000005428 wave function Effects 0.000 description 3
- LBDSQNRQXIKAGX-UHFFFAOYSA-N (2-methyl-3-prop-2-enoyloxypropyl) prop-2-enoate Chemical compound C=CC(=O)OCC(C)COC(=O)C=C LBDSQNRQXIKAGX-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
- 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
- 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
- GTELLNMUWNJXMQ-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical class OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCC(CO)(CO)CO GTELLNMUWNJXMQ-UHFFFAOYSA-N 0.000 description 2
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-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
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 239000012958 Amine synergist Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- RPCXWTMDDPNXMP-UHFFFAOYSA-N N,N-bis(methylamino)-2-methylideneoctanamide Chemical compound CNN(C(C(=C)CCCCCC)=O)NC RPCXWTMDDPNXMP-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 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 2
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000008366 benzophenones Chemical class 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 2
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 2
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical class OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 2
- 230000005281 excited state Effects 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 230000002427 irreversible effect Effects 0.000 description 2
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
- 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 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 239000002062 molecular scaffold Substances 0.000 description 2
- 239000002071 nanotube Substances 0.000 description 2
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 2
- 229960003424 phenylacetic acid Drugs 0.000 description 2
- 239000003279 phenylacetic acid Substances 0.000 description 2
- 238000000016 photochemical curing Methods 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000007348 radical reaction Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 230000027756 respiratory electron transport chain Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 2
- 150000003573 thiols Chemical class 0.000 description 2
- MXFQRSUWYYSPOC-UHFFFAOYSA-N (2,2-dimethyl-3-prop-2-enoyloxypropyl) prop-2-enoate Chemical class C=CC(=O)OCC(C)(C)COC(=O)C=C MXFQRSUWYYSPOC-UHFFFAOYSA-N 0.000 description 1
- HHQAGBQXOWLTLL-UHFFFAOYSA-N (2-hydroxy-3-phenoxypropyl) prop-2-enoate Chemical compound C=CC(=O)OCC(O)COC1=CC=CC=C1 HHQAGBQXOWLTLL-UHFFFAOYSA-N 0.000 description 1
- IQGIEMYBDGDBMR-UHFFFAOYSA-N (3-methyl-5-prop-2-enoyloxypentyl) prop-2-enoate Chemical compound C=CC(=O)OCCC(C)CCOC(=O)C=C IQGIEMYBDGDBMR-UHFFFAOYSA-N 0.000 description 1
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 1
- WXPWZZHELZEVPO-UHFFFAOYSA-N (4-methylphenyl)-phenylmethanone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=CC=C1 WXPWZZHELZEVPO-UHFFFAOYSA-N 0.000 description 1
- LAIJAUHBAWLPCO-UHFFFAOYSA-N (4-tert-butylcyclohexyl) prop-2-enoate Chemical compound CC(C)(C)C1CCC(OC(=O)C=C)CC1 LAIJAUHBAWLPCO-UHFFFAOYSA-N 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- NGQSLSMAEVWNPU-YTEMWHBBSA-N 1,2-bis[(e)-2-phenylethenyl]benzene Chemical compound C=1C=CC=CC=1/C=C/C1=CC=CC=C1\C=C\C1=CC=CC=C1 NGQSLSMAEVWNPU-YTEMWHBBSA-N 0.000 description 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
- VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-UHFFFAOYSA-N 0.000 description 1
- ZMLPKJYZRQZLDA-UHFFFAOYSA-N 1-(2-phenylethenyl)-4-[4-(2-phenylethenyl)phenyl]benzene Chemical group C=1C=CC=CC=1C=CC(C=C1)=CC=C1C(C=C1)=CC=C1C=CC1=CC=CC=C1 ZMLPKJYZRQZLDA-UHFFFAOYSA-N 0.000 description 1
- JHXJMPVUVKIGKC-UHFFFAOYSA-N 1-(4-tert-butylphenyl)-2-hydroxy-2-methylpropan-1-one Chemical compound CC(C)(C)C1=CC=C(C(=O)C(C)(C)O)C=C1 JHXJMPVUVKIGKC-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
- VKQJCUYEEABXNK-UHFFFAOYSA-N 1-chloro-4-propoxythioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C(OCCC)=CC=C2Cl VKQJCUYEEABXNK-UHFFFAOYSA-N 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 description 1
- YIKSHDNOAYSSPX-UHFFFAOYSA-N 1-propan-2-ylthioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(C)C YIKSHDNOAYSSPX-UHFFFAOYSA-N 0.000 description 1
- RHNJVKIVSXGYBD-UHFFFAOYSA-N 10-prop-2-enoyloxydecyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCCCCCOC(=O)C=C RHNJVKIVSXGYBD-UHFFFAOYSA-N 0.000 description 1
- STFXXRRQKFUYEU-UHFFFAOYSA-N 16-methylheptadecyl prop-2-enoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)C=C STFXXRRQKFUYEU-UHFFFAOYSA-N 0.000 description 1
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 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
- PUGOMSLRUSTQGV-UHFFFAOYSA-N 2,3-di(prop-2-enoyloxy)propyl prop-2-enoate Chemical class C=CC(=O)OCC(OC(=O)C=C)COC(=O)C=C PUGOMSLRUSTQGV-UHFFFAOYSA-N 0.000 description 1
- OVJHMJJVXOJMBB-UHFFFAOYSA-N 2-(1,3-dioxo-3a,4,5,6,7,7a-hexahydroisoindol-2-yl)ethyl prop-2-enoate Chemical compound C1CCCC2C(=O)N(CCOC(=O)C=C)C(=O)C21 OVJHMJJVXOJMBB-UHFFFAOYSA-N 0.000 description 1
- KEVOENGLLAAIKA-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl prop-2-enoate Chemical compound CCCCOCCOCCOC(=O)C=C KEVOENGLLAAIKA-UHFFFAOYSA-N 0.000 description 1
- URQQDYIVGXOEDA-UHFFFAOYSA-N 2-(2-ethenoxyethoxy)ethyl prop-2-enoate Chemical compound C=COCCOCCOC(=O)C=C URQQDYIVGXOEDA-UHFFFAOYSA-N 0.000 description 1
- FTALTLPZDVFJSS-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl prop-2-enoate Chemical compound CCOCCOCCOC(=O)C=C FTALTLPZDVFJSS-UHFFFAOYSA-N 0.000 description 1
- KJSGODDTWRXQRH-UHFFFAOYSA-N 2-(dimethylamino)ethyl benzoate Chemical compound CN(C)CCOC(=O)C1=CC=CC=C1 KJSGODDTWRXQRH-UHFFFAOYSA-N 0.000 description 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-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
- COORVRSSRBIIFJ-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]-1-methoxyethanol;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(O)COCCOCCO COORVRSSRBIIFJ-UHFFFAOYSA-N 0.000 description 1
- DDLCHCHDTHYPTF-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propyl prop-2-enoate Chemical compound COC(C)COC(C)COC(C)COC(=O)C=C DDLCHCHDTHYPTF-UHFFFAOYSA-N 0.000 description 1
- GLIKXZUJKIVGIE-UHFFFAOYSA-N 2-[2-(2-phenylethenyl)phenyl]-1,3-benzoxazole Chemical compound C=1C=CC=C(C=2OC3=CC=CC=C3N=2)C=1C=CC1=CC=CC=C1 GLIKXZUJKIVGIE-UHFFFAOYSA-N 0.000 description 1
- QGSPHUSCHLYIBI-UHFFFAOYSA-N 2-[2-(2-phenylethenyl)phenyl]benzo[e]benzotriazole Chemical compound C=1C=CC=C(N2N=C3C4=CC=CC=C4C=CC3=N2)C=1C=CC1=CC=CC=C1 QGSPHUSCHLYIBI-UHFFFAOYSA-N 0.000 description 1
- BRVWNIITDBKNRV-UHFFFAOYSA-N 2-[2-(2-phenylethenyl)phenyl]triazole Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1N1N=CC=N1 BRVWNIITDBKNRV-UHFFFAOYSA-N 0.000 description 1
- LKOQTCXPJVIMFO-UHFFFAOYSA-N 2-[2-[4-(dimethylamino)benzoyl]oxyethyl-methylamino]ethyl 4-(dimethylamino)benzoate Chemical compound C=1C=C(N(C)C)C=CC=1C(=O)OCCN(C)CCOC(=O)C1=CC=C(N(C)C)C=C1 LKOQTCXPJVIMFO-UHFFFAOYSA-N 0.000 description 1
- GSHSNSNNRMTERW-UHFFFAOYSA-N 2-[[1-oxo-1-(4-phenylsulfanylphenyl)octan-2-ylidene]amino]benzoic acid Chemical compound C=1C=C(SC=2C=CC=CC=2)C=CC=1C(=O)C(CCCCCC)=NC1=CC=CC=C1C(O)=O GSHSNSNNRMTERW-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
- ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 description 1
- SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 description 1
- ZCAKXIMITCASOU-UHFFFAOYSA-N 2-hydroxy-1-[4-(2-hydroxypropoxy)phenyl]-2-methylpropan-1-one Chemical compound CC(O)COC1=CC=C(C(=O)C(C)(C)O)C=C1 ZCAKXIMITCASOU-UHFFFAOYSA-N 0.000 description 1
- LYGZOGDWCOYSGJ-UHFFFAOYSA-N 2-hydroxy-1-[4-[4-(2-hydroxy-2-methylpropanoyl)phenoxy]phenyl]-2-methylpropan-1-one Chemical compound C1=CC(C(=O)C(C)(O)C)=CC=C1OC1=CC=C(C(=O)C(C)(C)O)C=C1 LYGZOGDWCOYSGJ-UHFFFAOYSA-N 0.000 description 1
- PCKZAVNWRLEHIP-UHFFFAOYSA-N 2-hydroxy-1-[4-[[4-(2-hydroxy-2-methylpropanoyl)phenyl]methyl]phenyl]-2-methylpropan-1-one Chemical compound C1=CC(C(=O)C(C)(O)C)=CC=C1CC1=CC=C(C(=O)C(C)(C)O)C=C1 PCKZAVNWRLEHIP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DPNXHTDWGGVXID-UHFFFAOYSA-N 2-isocyanatoethyl prop-2-enoate Chemical compound C=CC(=O)OCCN=C=O DPNXHTDWGGVXID-UHFFFAOYSA-N 0.000 description 1
- HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 description 1
- 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 1
- ZKYCLDTVJCJYIB-UHFFFAOYSA-N 2-methylidenedecanamide Chemical compound CCCCCCCCC(=C)C(N)=O ZKYCLDTVJCJYIB-UHFFFAOYSA-N 0.000 description 1
- GASMGDMKGYYAHY-UHFFFAOYSA-N 2-methylidenehexanamide Chemical compound CCCCC(=C)C(N)=O GASMGDMKGYYAHY-UHFFFAOYSA-N 0.000 description 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 1
- YHSYGCXKWUUKIK-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C=C YHSYGCXKWUUKIK-UHFFFAOYSA-N 0.000 description 1
- RXBOCDZLKBPILN-UHFFFAOYSA-N 2-propylheptyl prop-2-enoate Chemical compound CCCCCC(CCC)COC(=O)C=C RXBOCDZLKBPILN-UHFFFAOYSA-N 0.000 description 1
- VUEZBQJWLDBIDE-UHFFFAOYSA-N 3-ethenyl-1,3-oxazolidin-2-one Chemical compound C=CN1CCOC1=O VUEZBQJWLDBIDE-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
- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 1
- YDIYEOMDOWUDTJ-UHFFFAOYSA-N 4-(dimethylamino)benzoic acid Chemical compound CN(C)C1=CC=C(C(O)=O)C=C1 YDIYEOMDOWUDTJ-UHFFFAOYSA-N 0.000 description 1
- UIACIUMOCZUZSC-UHFFFAOYSA-N 4-[1,2-diphenyl-2-(2h-triazol-4-yl)ethenyl]-2h-triazole Chemical compound C1=NNN=C1C(C=1C=CC=CC=1)=C(C=1C=CC=CC=1)C1=NNN=C1 UIACIUMOCZUZSC-UHFFFAOYSA-N 0.000 description 1
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 1
- UZDMJPAQQFSMMV-UHFFFAOYSA-N 4-oxo-4-(2-prop-2-enoyloxyethoxy)butanoic acid Chemical compound OC(=O)CCC(=O)OCCOC(=O)C=C UZDMJPAQQFSMMV-UHFFFAOYSA-N 0.000 description 1
- JRSLDSNZKFSCGW-UHFFFAOYSA-N 4-phenylhexa-1,3,5-trien-3-ylbenzene Chemical compound C=1C=CC=CC=1C(C=C)=C(C=C)C1=CC=CC=C1 JRSLDSNZKFSCGW-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
- YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 1
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- CUXGDKOCSSIRKK-UHFFFAOYSA-N 7-methyloctyl prop-2-enoate Chemical compound CC(C)CCCCCCOC(=O)C=C CUXGDKOCSSIRKK-UHFFFAOYSA-N 0.000 description 1
- LVGFPWDANALGOY-UHFFFAOYSA-N 8-methylnonyl prop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C=C LVGFPWDANALGOY-UHFFFAOYSA-N 0.000 description 1
- PGDIJTMOHORACQ-UHFFFAOYSA-N 9-prop-2-enoyloxynonyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCCCCOC(=O)C=C PGDIJTMOHORACQ-UHFFFAOYSA-N 0.000 description 1
- NWEXGPDHZMOVQY-UHFFFAOYSA-N C(C=C)(=O)O.C(C=C)(=O)O.OCC(C(=O)OC(C(CO)(C)C)=O)(C)C Chemical compound C(C=C)(=O)O.C(C=C)(=O)O.OCC(C(=O)OC(C(CO)(C)C)=O)(C)C NWEXGPDHZMOVQY-UHFFFAOYSA-N 0.000 description 1
- VSYYFEWLFLZPBM-UHFFFAOYSA-N C(C=C)(=O)O.C(C=C)(=O)OC1C=CC=C1 Chemical compound C(C=C)(=O)O.C(C=C)(=O)OC1C=CC=C1 VSYYFEWLFLZPBM-UHFFFAOYSA-N 0.000 description 1
- DTHNRQCWKAOWSC-UHFFFAOYSA-N C(C=C)(=O)O.C1(=CC=CC=C1)C1=C(C=CC=C1)OC1=C(C=CC=C1)C1=CC=CC=C1 Chemical compound C(C=C)(=O)O.C1(=CC=CC=C1)C1=C(C=CC=C1)OC1=C(C=CC=C1)C1=CC=CC=C1 DTHNRQCWKAOWSC-UHFFFAOYSA-N 0.000 description 1
- RBUWQEHTCBTJBF-UHFFFAOYSA-N CCCC(=C)C(=O)N(NCC)NCC Chemical compound CCCC(=C)C(=O)N(NCC)NCC RBUWQEHTCBTJBF-UHFFFAOYSA-N 0.000 description 1
- XCMOXIRPSBLTEL-UHFFFAOYSA-N CCNN(NCC)C(=O)C(=C)CC Chemical compound CCNN(NCC)C(=O)C(=C)CC XCMOXIRPSBLTEL-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- UQBOJOOOTLPNST-UHFFFAOYSA-N Dehydroalanine Chemical class NC(=C)C(O)=O UQBOJOOOTLPNST-UHFFFAOYSA-N 0.000 description 1
- ZMDDERVSCYEKPQ-UHFFFAOYSA-N Ethyl (mesitylcarbonyl)phenylphosphinate Chemical compound C=1C=CC=CC=1P(=O)(OCC)C(=O)C1=C(C)C=C(C)C=C1C ZMDDERVSCYEKPQ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- NQSMEZJWJJVYOI-UHFFFAOYSA-N Methyl 2-benzoylbenzoate Chemical compound COC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 NQSMEZJWJJVYOI-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- NPKSPKHJBVJUKB-UHFFFAOYSA-N N-phenylglycine Chemical compound OC(=O)CNC1=CC=CC=C1 NPKSPKHJBVJUKB-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- VEPKQEUBKLEPRA-UHFFFAOYSA-N VX-745 Chemical compound FC1=CC(F)=CC=C1SC1=NN2C=NC(=O)C(C=3C(=CC=CC=3Cl)Cl)=C2C=C1 VEPKQEUBKLEPRA-UHFFFAOYSA-N 0.000 description 1
- SEEVRZDUPHZSOX-UHFFFAOYSA-N [1-[9-ethyl-6-(2-methylbenzoyl)carbazol-3-yl]ethylideneamino] acetate Chemical compound C=1C=C2N(CC)C3=CC=C(C(C)=NOC(C)=O)C=C3C2=CC=1C(=O)C1=CC=CC=C1C SEEVRZDUPHZSOX-UHFFFAOYSA-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
- VLVZXTNDRFWYLF-UHFFFAOYSA-N [2-ethyl-2-(prop-2-enoyloxymethyl)hexyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CC)(CCCC)COC(=O)C=C VLVZXTNDRFWYLF-UHFFFAOYSA-N 0.000 description 1
- QIPOUSKNIMYTRA-UHFFFAOYSA-N [2-hydroxy-3-[4-(2-hydroxy-3-prop-2-enoyloxypropoxy)butoxy]propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(O)COCCCCOCC(O)COC(=O)C=C QIPOUSKNIMYTRA-UHFFFAOYSA-N 0.000 description 1
- BBFOCXUSMHSHGM-UHFFFAOYSA-N [3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C BBFOCXUSMHSHGM-UHFFFAOYSA-N 0.000 description 1
- KNSXNCFKSZZHEA-UHFFFAOYSA-N [3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical class C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C KNSXNCFKSZZHEA-UHFFFAOYSA-N 0.000 description 1
- LXSJHLYEDBJAGK-UHFFFAOYSA-N [4-(2-phenylpropan-2-yl)phenyl] prop-2-enoate Chemical class C=1C=C(OC(=O)C=C)C=CC=1C(C)(C)C1=CC=CC=C1 LXSJHLYEDBJAGK-UHFFFAOYSA-N 0.000 description 1
- GUCYFKSBFREPBC-UHFFFAOYSA-N [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C(=O)C1=C(C)C=C(C)C=C1C GUCYFKSBFREPBC-UHFFFAOYSA-N 0.000 description 1
- 238000000862 absorption spectrum Methods 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
- 150000003926 acrylamides Chemical group 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation 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
- VYHBFRJRBHMIQZ-UHFFFAOYSA-N bis[4-(diethylamino)phenyl]methanone Chemical compound C1=CC(N(CC)CC)=CC=C1C(=O)C1=CC=C(N(CC)CC)C=C1 VYHBFRJRBHMIQZ-UHFFFAOYSA-N 0.000 description 1
- 229930006711 bornane-2,3-dione Natural products 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000005493 condensed matter Effects 0.000 description 1
- 150000001893 coumarin derivatives Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- KHAYCTOSKLIHEP-UHFFFAOYSA-N docosyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=C KHAYCTOSKLIHEP-UHFFFAOYSA-N 0.000 description 1
- DBNQCTQALGGHMH-UHFFFAOYSA-N dodecanoic acid;(4-hydroxyphenyl)-phenylmethanone Chemical compound CCCCCCCCCCCC(O)=O.C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 DBNQCTQALGGHMH-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001227 electron beam curing Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000035558 fertility Effects 0.000 description 1
- 210000003754 fetus Anatomy 0.000 description 1
- 238000007647 flexography Methods 0.000 description 1
- YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 1
- GNNILMDCYQGMRH-UHFFFAOYSA-N formyl benzoate Chemical class O=COC(=O)C1=CC=CC=C1 GNNILMDCYQGMRH-UHFFFAOYSA-N 0.000 description 1
- 239000003574 free electron Substances 0.000 description 1
- 238000012682 free radical photopolymerization Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- YLHXLHGIAMFFBU-UHFFFAOYSA-N methyl phenylglyoxalate Chemical compound COC(=O)C(=O)C1=CC=CC=C1 YLHXLHGIAMFFBU-UHFFFAOYSA-N 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- LZSOYZHJAUFJOR-UHFFFAOYSA-N n,n-bis(ethylaminomethyl)prop-2-enamide Chemical compound CCNCN(C(=O)C=C)CNCC LZSOYZHJAUFJOR-UHFFFAOYSA-N 0.000 description 1
- DFENKTCEEGOWLB-UHFFFAOYSA-N n,n-bis(methylamino)-2-methylidenepentanamide Chemical compound CCCC(=C)C(=O)N(NC)NC DFENKTCEEGOWLB-UHFFFAOYSA-N 0.000 description 1
- GKWLJNRLFBQTEI-UHFFFAOYSA-N n,n-bis(methylaminomethyl)prop-2-enamide Chemical compound CNCN(CNC)C(=O)C=C GKWLJNRLFBQTEI-UHFFFAOYSA-N 0.000 description 1
- DLJMSHXCPBXOKX-UHFFFAOYSA-N n,n-dibutylprop-2-enamide Chemical compound CCCCN(C(=O)C=C)CCCC DLJMSHXCPBXOKX-UHFFFAOYSA-N 0.000 description 1
- OVHHHVAVHBHXAK-UHFFFAOYSA-N n,n-diethylprop-2-enamide Chemical compound CCN(CC)C(=O)C=C OVHHHVAVHBHXAK-UHFFFAOYSA-N 0.000 description 1
- ZLSJVVLETDAEQY-UHFFFAOYSA-N n,n-dihexylprop-2-enamide Chemical compound CCCCCCN(C(=O)C=C)CCCCCC ZLSJVVLETDAEQY-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
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- KCTMTGOHHMRJHZ-UHFFFAOYSA-N n-(2-methylpropoxymethyl)prop-2-enamide Chemical compound CC(C)COCNC(=O)C=C KCTMTGOHHMRJHZ-UHFFFAOYSA-N 0.000 description 1
- UTSYWKJYFPPRAP-UHFFFAOYSA-N n-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCNC(=O)C=C UTSYWKJYFPPRAP-UHFFFAOYSA-N 0.000 description 1
- FPLFMJUPDWYPHQ-UHFFFAOYSA-N n-[2-(2-phenylethenyl)phenyl]triazin-4-amine Chemical compound C=1C=CC=C(C=CC=2C=CC=CC=2)C=1NC1=CC=NN=N1 FPLFMJUPDWYPHQ-UHFFFAOYSA-N 0.000 description 1
- WDQKICIMIPUDBL-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]prop-2-enamide Chemical compound CN(C)CCNC(=O)C=C WDQKICIMIPUDBL-UHFFFAOYSA-N 0.000 description 1
- OHLHOLGYGRKZMU-UHFFFAOYSA-N n-benzylprop-2-enamide Chemical compound C=CC(=O)NCC1=CC=CC=C1 OHLHOLGYGRKZMU-UHFFFAOYSA-N 0.000 description 1
- PMJFVKWBSWWAKT-UHFFFAOYSA-N n-cyclohexylprop-2-enamide Chemical compound C=CC(=O)NC1CCCCC1 PMJFVKWBSWWAKT-UHFFFAOYSA-N 0.000 description 1
- XQPVIMDDIXCFFS-UHFFFAOYSA-N n-dodecylprop-2-enamide Chemical compound CCCCCCCCCCCCNC(=O)C=C XQPVIMDDIXCFFS-UHFFFAOYSA-N 0.000 description 1
- SWPMNMYLORDLJE-UHFFFAOYSA-N n-ethylprop-2-enamide Chemical compound CCNC(=O)C=C SWPMNMYLORDLJE-UHFFFAOYSA-N 0.000 description 1
- GCGQYJSQINRKQL-UHFFFAOYSA-N n-hexylprop-2-enamide Chemical compound CCCCCCNC(=O)C=C GCGQYJSQINRKQL-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- AWGZKFQMWZYCHF-UHFFFAOYSA-N n-octylprop-2-enamide Chemical compound CCCCCCCCNC(=O)C=C AWGZKFQMWZYCHF-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 1
- WDFKEEALECCKTJ-UHFFFAOYSA-N n-propylprop-2-enamide Chemical compound CCCNC(=O)C=C WDFKEEALECCKTJ-UHFFFAOYSA-N 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 239000000820 nonprescription drug Substances 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- DNPFOADIPJWGQH-UHFFFAOYSA-N octan-3-yl prop-2-enoate Chemical class CCCCCC(CC)OC(=O)C=C DNPFOADIPJWGQH-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- RZFODFPMOHAYIR-UHFFFAOYSA-N oxepan-2-one;prop-2-enoic acid Chemical compound OC(=O)C=C.O=C1CCCCCO1 RZFODFPMOHAYIR-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- JZDGWLGMEGSUGH-UHFFFAOYSA-N phenyl-(2,4,6-trimethylbenzoyl)phosphinic acid Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(O)(=O)C1=CC=CC=C1 JZDGWLGMEGSUGH-UHFFFAOYSA-N 0.000 description 1
- HPAFOABSQZMTHE-UHFFFAOYSA-N phenyl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)C1=CC=CC=C1 HPAFOABSQZMTHE-UHFFFAOYSA-N 0.000 description 1
- LYXOWKPVTCPORE-UHFFFAOYSA-N phenyl-(4-phenylphenyl)methanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 LYXOWKPVTCPORE-UHFFFAOYSA-N 0.000 description 1
- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical class OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 description 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
- 238000007146 photocatalysis Methods 0.000 description 1
- 238000001782 photodegradation Methods 0.000 description 1
- FSDNTQSJGHSJBG-UHFFFAOYSA-N piperidine-4-carbonitrile Chemical compound N#CC1CCNCC1 FSDNTQSJGHSJBG-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920005650 polypropylene glycol diacrylate Polymers 0.000 description 1
- 239000000955 prescription drug Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- QFXCGXNPCMKTJQ-UHFFFAOYSA-N prop-2-enoic acid;1,1,3-trimethylcyclohexane Chemical compound OC(=O)C=C.CC1CCCC(C)(C)C1 QFXCGXNPCMKTJQ-UHFFFAOYSA-N 0.000 description 1
- QCTJRYGLPAFRMS-UHFFFAOYSA-N prop-2-enoic acid;1,3,5-triazine-2,4,6-triamine Chemical compound OC(=O)C=C.NC1=NC(N)=NC(N)=N1 QCTJRYGLPAFRMS-UHFFFAOYSA-N 0.000 description 1
- UFUASNAHBMBJIX-UHFFFAOYSA-N propan-1-one Chemical compound CC[C]=O UFUASNAHBMBJIX-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- RSVDRWTUCMTKBV-UHFFFAOYSA-N sbb057044 Chemical compound C12CC=CC2C2CC(OCCOC(=O)C=C)C1C2 RSVDRWTUCMTKBV-UHFFFAOYSA-N 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000001338 self-assembly Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000013501 sustainable material Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical class C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- XOALFFJGWSCQEO-UHFFFAOYSA-N tridecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C=C XOALFFJGWSCQEO-UHFFFAOYSA-N 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
Classifications
-
- 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
- C09D11/00—Inks
- C09D11/52—Electrically conductive inks
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
- C09D11/037—Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/06—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
- B05D3/061—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation using U.V.
- B05D3/065—After-treatment
- B05D3/067—Curing or cross-linking the coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/0081—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using electromagnetic radiation or waves, e.g. ultraviolet radiation, electron beams
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/346—Clay
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- 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
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2217—Oxides; Hydroxides of metals of magnesium
- C08K2003/222—Magnesia, i.e. magnesium oxide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2237—Oxides; Hydroxides of metals of titanium
- C08K2003/2241—Titanium dioxide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2296—Oxides; Hydroxides of metals of zinc
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Toxicology (AREA)
- General Health & Medical Sciences (AREA)
- Electromagnetism (AREA)
- Dispersion Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Polymerisation Methods In General (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
本明細書に記載されているのは、化学線への曝露によって硬化可能であるインクおよびコーティングなどの、化学線硬化性組成物である。組成物は、エチレン性不飽和モノマー、エチレン性不飽和プレポリマー、およびそれらの組み合わせから選択される重合性構成成分と、
MxOyHz(I)
式中、Mが、Ti、Zn、Mg、Ce、Bi、およびFeから選択される金属であり、
Oが、酸素であり、
Hが、ハロゲンであり、
xが、1~3の整数であり、
yが、1~3の整数であり、
zが、0~3の整数である。
MxOyHz(I)
式中、Mが、Ti、Zn、Mg、Ce、Bi、およびFeから選択される金属であり、
Oが、酸素であり、
Hが、ハロゲンであり、
xが、1~3の整数であり、
yが、1~3の整数であり、
zが、0~3の整数である。
式(I)で定義される金属酸化物の組み合わせを使用してもよい。
一態様では、重合性構成成分は、組成物の総重量に基づいて、10重量%~90重量%、好ましくは60重量%~90重量%、より好ましくは70重量%~90重量%の量で化学線硬化性組成物中に存在する。
好適な単官能性エチレン性不飽和モノマーの例としては、限定されないが、以下が挙げられる:
オリゴマーからなる少なくとも1種のプレポリマーは、好ましくは、エポキシアクリレート、アクリル化油、ウレタンアクリレート(脂肪族および芳香族)、ポリエステルアクリレート、ポリエーテルアクリレート、ビニル/アクリルオリゴマー、ポリエン/チオール系、およびそれらの組み合わせからなる群から選択され得る。
本組成物は、1種以上の光開始剤を含み得る。一態様では、光開始剤構成成分は、組成物の総重量に基づいて、2.0重量%~40重量%、好ましくは5.0重量%~25重量%、より好ましくは5.0重量%~20重量%の量で化学線硬化性組成物中に存在する。さらなる態様では、この量は、記載の半導体金属酸化物材料およびその複合材を含まない化学線硬化性組成物中に提供される光開始剤の量よりも少ない。
化学線硬化性組成物は、1つ以上の機能を実施し、かつ/または組成物に1つ以上の属性を提供する他の構成成分を含んでもよい。それらには、以下がある。
アミン相乗剤もまた、配合物に含まれ得る。好適な例としては、限定されないが、以下が挙げられる:2-(ジメチルアミノ)エチルベンゾエートなどの芳香族アミン、N-フェニルグリシン、安息香酸、4-(ジメチルアミノ)-、1,1’[(メチルイミノ)ジ-2,1-エタンジイル]エステル、ならびに4-(N,N-ジメチルアミノ)安息香酸と、エチル、アミル、2-ブトキシエチル、および特に好ましくは2-エチルヘキシルエステルとの単純なアルキルエステル、N,N-ジメチルアミノ)安息香酸エステルの他の位置異性体も好適である。
好適な着色剤としては、限定されないが、有機または無機顔料および染料が挙げられる。染料は、蛍光染料、アゾ染料、アントラキノン染料、キサンテン染料、アジン染料、それらの組み合わせなどを含むが、これらに限定されない。有機顔料は、例えば、Pigment Yellow No.12、13、14、17、74、83、114、126、127、174、188、Pigment Red No.2、22、23、48:1、48:2、52、52:1、53、57:1、112、122、166、170、184、202、266、269、Pigment Orange No.5、16、34、36、Pigment Blue No.15、15:3、15:4、Pigment Violet No.3、23、27、および/またはPigment Green No.7などの1つの顔料または顔料の組み合わせであってよい。無機顔料は、以下の非限定的な顔料の1つであり得る:酸化鉄、二酸化チタン、酸化クロム、フェロシアン化第二鉄アンモニウム、黒色酸化第二鉄、Pigment Black No.7ならびに/またはPigment White No.6および7。所望の色を達成する組み合わせと同様に、他の有機および無機の顔料および染料も、採用され得る。
化学線で硬化可能な組成物はまた、蛍光増白剤を含んでもよい。蛍光増白剤は、UV範囲で吸収し、吸収されたUV光の大部分を400~500nmの波長を有する青色の蛍光として再放射する無色または青白い有機化合物であることが知られている。発光検出器はUV光を放射し、生じる蛍光を検出することができる。好適な蛍光増白剤の例としては、ジスチリルベンゼン、ジスチリルビフェニル、ジビニルスチルベン、トリアジニルアミノスチルベン、スチルベニル-2H-トリアゾール、スチルベニル-2H-ナフト[1,2-d]トリアゾール、およびビス(1,2,3-トリアゾリル)スチルベンなどのスチルベン誘導体が挙げられ、これらの各々は、さらに置換されていてもよい。さらなる例としては、ベンゾオキサゾール、スチルベニルベンゾオキサゾール、ビスベンゾオキサゾール、ベンズイミダゾール誘導体、ピラゾリン誘導体、またはクマリン誘導体が挙げられる。蛍光増白剤は、例えば、Blankophor(登録商標)、Tinopal(登録商標)、またはUltraphor(登録商標)の名称で市販されている。異なる蛍光増白剤の混合物も使用することができる。使用される蛍光増白剤の量は、通常、組成物の総重量に基づいて、1.0重量%~25重量%である。
化学線で硬化可能な組成物はまた、限定されないが、アミドワックス、エルカミドワックス、ポリプロピレンワックス、パラフィンワックス、ポリエチレンワックス、TEFLON(登録商標)、カルナウバワックスなどのワックスを含んでもよい。ワックスは、上記ワックスの組み合わせであってよい。ワックスは、アミドワックスとエルカミドワックスとのブレンドであることが好ましい。ワックスは、存在する場合、0重量%~4.0重量%の量である。ワックスは、0.1重量%~約2.0重量%の量で存在することが好ましい。
化学線で硬化可能な組成物のほとんどと同じように、添加剤を組み込んで様々な特性を向上することができる。かかる添加剤の部分的な列挙としては、限定されないが、接着促進剤、シリコーン、光安定剤、脱気添加剤、アンモニア、流動促進剤、消泡剤、酸化防止剤、安定剤、界面活性剤、分散剤、可塑剤、レオロジー添加剤、ワックス、シリコーンなどが挙げられる。
本発明の化学線硬化性組成物は、例えば日光などの可視光、ならびに高電圧水銀電球、中電圧水銀電球、キセノン電球、カーボンアークランプ、金属ハロゲン化物電球、およびUV-LED光源によって提供され得るUV光などの化学線光源によって放射される光への曝露によって、硬化させることができる。組成物はまた、電子ビーム(EB)放射線への曝露によって硬化させてもよい。
上の表1に記載のBGA1を1%wtでHDDAに添加した。325nm~500nmの波長のUVパルスを、0.5秒間隔で放射した。光DSCスペクトル(TA Instruments、Q2000)が発生し、それは図1である。示されているように、半導体TiO2金属酸化物の存在下でHDDAがUVフリーラジカル光化学重合を受けると、固有の熱特性が観察された(上の曲線、図1)。対照的に、半導体材料が存在しない状態でHDDAがUV光に曝露すると、熱特性は見られない(下の曲線、図1)。これは、BGA1複合材で重合反応が生じ、結合が作り出され、熱が放出されていることの証拠である。
シアン1中0.5%のBGA1を、3枚の基材上にLittle Joeでプルーフィングし、100fpm、200W/インチ、および200mJ/cm2のHg UVランプでUV硬化させた。
ブラック1中の光開始剤含有量を10%低減し、次いで3%のZn1をブラック1に添加し、これをSBSの上に「Little Joe」でプルーフィングし、100fpm、200W/インチ、および200mJ/cm2のHg UVランプでUV硬化させた。比較を提供するために、同じ様式でZn1を添加していないブラック1をプルーフィングし、硬化させた。光開始剤の濃度は、ブラック1よりも10%低減させた。表4は、試験結果を含む。
本発明実施例4
5%のBGA2をマゼンタ1に追加した。Little Joeを使用してSBS上にEBリソグラフィーインクをプルーフィングし、30ppmの酸素および50kGyの照射線量のEBによって硬化させた。マゼンタ1をSBS上にプルーフィングし、比較を提供するために硬化させた。
2.5%の半導性ZnO(Zn1)をブラック2に添加し、UV硬化性フレキソグラフィーインクを白色の延伸ポリプロピレンフィルム(OPP)上にプルーフィングし、100fpm、200W/インチ、および200mJ/cm2ノHg UVランプで硬化させた。ブラック2をOPP上にプルーフィングし、比較を提供するために硬化させた。
6%のBGA3(半導性TiO2、半導性ZnO、およびアルミノケイ酸塩粘土ナノチューブ)をブラック3に添加し、3回圧延粉砕した。PPプラスチックカップを平らなシートに切断し、基材を26fpmおよび0.42kWのユニットに2回ユニットに通すことによる、Enerconへの2回の通過を使用して、コロナ処理した。インクを、IGTプルーファーを使用してPP上にプルーフィングし、400ワット/インチ(wpi)、200fpmで硬化させた。ブラック3を同じPP基材上にプルーフィングし、比較を提供するために硬化させた。
ブラック3から2.4%のIrgacure369を除去し、次いで2.4%のBGA3をインクに添加し、DACミキサーを使用してインクに混合した。PPプラスチックカップを平らなシートに切断し、基材を26fpmおよび0.42kWのユニットに2回ユニットに通すことによる、Enerconへの2回の通過で、コロナ処理した。インクを、IGTを使用してPP上にプルーフィングし、400wpi、200fpmで硬化させた。比較のために、2.4%のIrgacure369を含有するブラック3インクを、同じPP基材上にプルーフィングし、硬化させて比較を提供した。
UVフレキソブラック4は、5%のIrgacure369を含む。本発明実施例9では、UVフレキソブラック4中の5%のIrgacure369を5%のBGA3に置き換えた。Harperフレキソハンドプルーファーを使用して、700lpi、2.2bcmのアニロックスでコロナ処理したPETフィルム上に実施例9をプルーフィングし、400wpiおよび300fpmのベルト速度で硬化させた。印刷物は、硬化ユニットを複数回通過させ、各印刷ユニットの後にインク/基材をUVランプの下を通過させるプレスで、インクがどのように見えるかを複製したものであった。比較のために、5%のIrgacure369を含有するブラック4を、同じPET基材上にプルーフィングし、硬化させて比較を提供した。
エトキシル化トリメチロールプロパントリアクリレート(EOTMPTA)中50%のBGA1分散液を、DACミキサーで混合することによって調製した。この混合物をシアン2インクに5%添加し、DACミキサーで混合した。Harperフレキソハンドプルーファーを使用して、700lpi、2.2bcmのアニロックスでコロナ処理したPETフィルム上にインクをプルーフィングし、100fpmのUV LED硬化ユニットで硬化させた。シアン2を同じPET基材上にプルーフィングし、比較を提供するために硬化させた。
5%のBGA1をEOTMPTAに添加した。可視光パルスは、1.0秒間隔、5%の光強度で10サイクル、400nm~500nmで放射し、光DSC熱放射を測定した(TA Instruments、Q2000)。パンおよびEOTMPTAの熱特性を差し引き、曲線下面積を合計した。mW/gの単位は、結合が形成されるときの反応エンタルピーに関連し、硬化熱としても知られている。5%のBGA1の代わりに5%のBi2(Bi2O3)を用いて、上の手順を繰り返した。結果を表12に提供する。
UV硬化性接着剤組成物は、インクおよびコーティングを作製するために使用されるものに匹敵する材料で配合されている。提示された結果に基づいて、半導体金属酸化物材料を既存の光開始剤パッケージに添加して増加させるか、または一部の光開始剤を置き換えると、硬化を維持しながらも、硬化の改善が可能であるはずである。
Claims (22)
- エチレン性不飽和モノマー、エチレン性不飽和プレポリマー、およびそれらの組み合わせから選択される重合性構成成分と、
1つ以上の染料又は顔料と、
(a)下記式(I)で定義される1つ以上の半導体金属酸化物と、(b)カーボンブラック、リソールルビン、アルミノケイ酸塩粘土、フミン酸、フミン酸ポリマーおよびそれらの組み合わせから選択される成分とを含む、複合光触媒材料と、
MxOyHz(I)
(式中、Mが、Ti、Zn、Mg、Ce、Bi、およびFeから選択される金属であり、
Oが、酸素であり、
Hが、ハロゲンであり、
xが、1~3の整数であり、
yが、1~3の整数であり、
zが、0~3の整数である。)
を含む、化学線への曝露によって硬化可能な組成物であって、
前記半導体金属酸化物が、反応開始照射線量の化学線に曝露されたとき、前記半導体金属酸化物が失われることなく、前記重合性構成成分中に、フリーラジカル重合反応経路を生成し、
前記組成物が、印刷インク、コーティング、接着剤、またはプライマー組成物であり、
前記半導体金属酸化物が、前記重合性構成成分と直接相互作用する、組成物。 - 前記式(I)で定義される半導体金属酸化物の組み合わせが存在する、請求項1に記載の組成物。
- 前記成分(b)が、カーボンブラック、アルミノケイ酸塩粘土、およびそれらの組み合わせから選択される、請求項1に記載の組成物。
- 前記複合光触媒材料が、
半導性TiO2およびカーボンブラックを含む複合材、
半導性TiO2、半導性BiOCl、半導性Bi2O3、半導性MgO、半導性ZnOおよびカーボンブラックを含む複合材、ならびに
半導性TiO2、半導性ZnO、およびアルミノケイ酸塩粘土を含む複合材
から選択された複合材である、請求項1に記載の組成物。 - 前記重合性構成成分が、単官能性エチレン性不飽和モノマー、および多官能性エチレン性不飽和モノマーから選択されるエチレン性不飽和モノマーを含む、請求項1に記載の組成物。
- 前記重合性構成成分が、10重量%~90重量%の量で存在する、請求項1に記載の組成物。
- 前記重合性構成成分が、エチレン性不飽和プレポリマーを含む、請求項1に記載の組成物。
- 前記重合性構成成分が、エチレン性不飽和モノマーおよびエチレン性不飽和プレポリマーを含む、請求項1に記載の組成物。
- 前記重合性構成成分が、エポキシアクリレート、アクリル基を有する油、脂肪族ウレタンアクリレート、芳香族ウレタンアクリレート、ポリエステルアクリレート、ポリエーテルアクリレート、ビニル/アクリルオリゴマー、ポリエン/チオール系、およびそれらの組み合わせから選択されるエチレン性不飽和プレポリマーを含む、請求項1に記載の組成物。
- 蛍光染料、アゾ染料、アントラキノン染料、キサンテン染料、アジン染料およびこれらの組み合わせから選択される1つ以上の染料、
及び/又は
Pigment Yellow No.12、13、14、17、74、83、114、126、127、174および188、Pigment Red No.2、22、23、48:1、48:2、52、52:1、53、57:1、112、122、166、170、184、202、266および269、Pigment Orange No.5、16、34および36、Pigment Blue No.15、15:3および15:4、Pigment Violet No.3、23および27、Pigment Green No.7、Pigment Black No.7、Pigment White No.6および7、酸化鉄、二酸化チタン、酸化クロム、フェロシアン化第二鉄アンモニウムおよび黒色酸化第二鉄、FD&C Red No.40、FD&C Yellow No.5、FD&C Yellow No.6およびFD&C Blue No.1、D&C Red No.6、D&C Red No.7、D&C Red No.21、D&C Red No.22、D&C Red No.27、Red No.28、D&C Red No.30、D&C Red No.33、D&C Red No.34、D&C Red No.36、D&C Orange No.5、およびD&C Yellow No.10並びにこれらの組み合わせから選択される1つ以上の顔料
を含む、請求項1に記載の組成物。 - 前記顔料を含む、請求項10に記載の組成物。
- 前記光触媒材料が、0.1重量%~25重量%の量で存在する、請求項1に記載の組成物。
- 1種以上の光開始剤を含む光開始剤構成成分をさらに含む、請求項1に記載の組成物。
- 前記光開始剤構成成分が、2.0重量%~40重量%の量で存在する、請求項13に記載の組成物。
- 前記組成物が、2-ベンジル-2-ジメチルアミノ-1-(4-モルホリノフェニル)-ブタノン-1から選択される光開始剤を含まない、請求項1に記載の組成物。
- 前記組成物が、UVランプ、UVレーザー、UV-LED、可視光、太陽光、電子ビーム、およびそれらの組み合わせから選択される光源によって放射される光への曝露によって硬化可能である、請求項1に記載の組成物。
- 前記組成物が、高電圧水銀電球、中電圧水銀電球、キセノン電球、カーボンアークランプ、メタルハライド電球、UV-LEDランプ、およびUVレーザーから選択される光源によって放射されるUV光への曝露によって硬化可能である、請求項1に記載の組成物。
- 前記組成物が、10kGy~40kGyの照射線量での電子ビーム放射線への曝露によって硬化可能である、請求項1に記載の組成物。
- 請求項1に記載の組成物で印刷された基材を含む、印刷物品。
- 前記基材が、プラスチック、セルロース、紙、厚紙、および金属から選択される、請求項19に記載の印刷物品。
- 前記基材が、パッケージ物品、金属パネル、および電子物品から選択される、請求項19に記載の印刷物品。
- 前記半導体金属酸化物が、ZnO、TiO2、BiOCl、Bi2O3、MgOまたはFe2O3を含む、請求項1に記載の組成物。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2022021172A JP2022060346A (ja) | 2018-05-10 | 2022-02-15 | 半導体金属酸化物材料を含む化学線硬化性組成物 |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862669533P | 2018-05-10 | 2018-05-10 | |
US62/669,533 | 2018-05-10 | ||
US201862740996P | 2018-10-04 | 2018-10-04 | |
US62/740,996 | 2018-10-04 | ||
PCT/US2019/012849 WO2019216961A1 (en) | 2018-05-10 | 2019-01-09 | Actinic radiation curable compositions including semiconductor metal oxide materials |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2022021172A Division JP2022060346A (ja) | 2018-05-10 | 2022-02-15 | 半導体金属酸化物材料を含む化学線硬化性組成物 |
JP2024051280A Division JP2024086743A (ja) | 2018-05-10 | 2024-03-27 | 半導体金属酸化物材料を含む化学線硬化性組成物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2021517200A JP2021517200A (ja) | 2021-07-15 |
JP7499187B2 true JP7499187B2 (ja) | 2024-06-13 |
Family
ID=68468204
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2020561889A Active JP7499187B2 (ja) | 2018-05-10 | 2019-01-09 | 半導体金属酸化物材料を含む化学線硬化性組成物 |
JP2022021172A Pending JP2022060346A (ja) | 2018-05-10 | 2022-02-15 | 半導体金属酸化物材料を含む化学線硬化性組成物 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2022021172A Pending JP2022060346A (ja) | 2018-05-10 | 2022-02-15 | 半導体金属酸化物材料を含む化学線硬化性組成物 |
Country Status (5)
Country | Link |
---|---|
US (1) | US11254830B2 (ja) |
EP (1) | EP3814023A4 (ja) |
JP (2) | JP7499187B2 (ja) |
BR (1) | BR112020022464A2 (ja) |
WO (1) | WO2019216961A1 (ja) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019216961A1 (en) * | 2018-05-10 | 2019-11-14 | Sun Chemical Corporation | Actinic radiation curable compositions including semiconductor metal oxide materials |
JP2021105710A (ja) * | 2019-12-26 | 2021-07-26 | 住友化学株式会社 | 感光性組成物 |
CN111662632B (zh) * | 2020-05-20 | 2022-03-08 | 中牟县美林包装有限责任公司 | 一种包装箱局部逆向uv印刷方法 |
CN115193453A (zh) * | 2022-07-13 | 2022-10-18 | 云南大学 | 一种生物炭基光催化剂及制备方法、RhB敏化生物炭基光催化剂及制备方法和应用 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3041172A (en) | 1958-12-30 | 1962-06-26 | Gen Aniline & Film Corp | Photopolymerization of vinyl monomers with metal oxides as catalysts |
US3147119A (en) | 1962-05-18 | 1964-09-01 | Gen Aniline & Film Corp | Photopolymerization of vinyl monomers with metal oxides as catalysts |
US3346383A (en) | 1960-11-23 | 1967-10-10 | Eastman Kodak Co | Image reproduction processes utilizing photopolymerization of vinyl monomer compositions comprising a metallic sulfide compound |
US4257915A (en) | 1979-07-23 | 1981-03-24 | E. I. Du Pont De Nemours And Company | Photopolymer initiator system containing a semiconductor, a reducing agent and an oxidizing agent |
JP2006219855A (ja) | 2005-02-09 | 2006-08-24 | Marutama Sangyo Kk | 木質系床材とその製造法 |
JP5234714B2 (ja) | 2007-02-21 | 2013-07-10 | 三菱重工印刷紙工機械株式会社 | 印刷機 |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3083113A (en) | 1960-04-07 | 1963-03-26 | Dorst W | Zinc oxide pigments and their production |
JPS5234714A (en) * | 1975-09-12 | 1977-03-16 | Kansai Paint Co Ltd | Photosensitive composition |
US4959297A (en) | 1987-12-09 | 1990-09-25 | Minnesota Mining And Manufacturing Company | Ternary photoinitiator system for addition polymerization |
US4889792A (en) * | 1987-12-09 | 1989-12-26 | Minnesota Mining And Manufacturing Company | Ternary photoinitiator system for addition polymerization |
JPH041204A (ja) * | 1990-04-19 | 1992-01-06 | Canon Inc | 光重合性樹脂組成物および記録媒体 |
US5212212A (en) | 1992-11-14 | 1993-05-18 | Lord Corporation | Zinc-containing ceramic ink compositions stabilized with calcium organic complex |
JPH08283453A (ja) * | 1995-04-14 | 1996-10-29 | Sekisui Chem Co Ltd | 抗菌性樹脂組成物 |
JPH10186426A (ja) | 1996-10-24 | 1998-07-14 | Mitsui Chem Inc | 光重合性樹脂組成物 |
AUPO688997A0 (en) | 1997-05-20 | 1997-06-12 | Soltec Research Pty Ltd | Sunscreen composition |
US6433038B1 (en) * | 1999-03-16 | 2002-08-13 | Seiko Epson Corporation | Photocurable ink composition for ink jet recording and ink jet recording method using the same |
JP2001075281A (ja) * | 1999-09-02 | 2001-03-23 | Kansai Paint Co Ltd | 光硬化性樹脂組成物及び光硬化塗膜 |
JP2003096119A (ja) * | 2001-09-27 | 2003-04-03 | Kuraray Co Ltd | 光硬化性の組成物 |
WO2005061602A1 (en) | 2003-12-24 | 2005-07-07 | Micronisers Pty Ltd | Acrylic compositions comprising nanoparticulate zinc oxide uv absorber |
US8128998B2 (en) | 2004-01-12 | 2012-03-06 | Ecolab Usa Inc. | Polyurethane coating cure enhancement using ultrafine zinc oxide |
US7816418B2 (en) | 2006-08-31 | 2010-10-19 | Ppg Industries Ohio, Inc. | Universal primer |
JP2007231178A (ja) * | 2006-03-01 | 2007-09-13 | Nara Institute Of Science & Technology | 光重合性組成物及び光重合方法 |
US7635504B2 (en) | 2006-05-05 | 2009-12-22 | E. I. Du Pont De Nemours And Company | Curable white inkjet ink |
US8512467B2 (en) | 2006-08-21 | 2013-08-20 | Air Products And Chemicals, Inc. | Zinc oxide nanoparticle dispersions |
WO2008062871A1 (fr) | 2006-11-22 | 2008-05-29 | Shiseido Company Ltd. | Procédé de production d'une poudre de fines particules d'oxyde de zinc et de cosmétiques contenant la poudre |
US8414981B2 (en) * | 2007-08-17 | 2013-04-09 | Prc Desoto International, Inc. | Multilayer coatings suitable for aerospace applications |
EP2368919A1 (de) | 2010-03-25 | 2011-09-28 | Universität des Saarlandes | Nanopartikuläre Photoinitiatoren |
US20120177928A1 (en) | 2010-08-16 | 2012-07-12 | Honeywell International Inc. | Hydrophilic and self cleaning uv nano-epoxy/acrylate cationic hybrid coating compositions for transparent polymeric materials, methods for forming coated transparent polymeric materials using such coating compositions, and coated transparent polymeric materials |
US8906468B2 (en) * | 2011-10-27 | 2014-12-09 | Ppg Industries Ohio, Inc. | Low gloss UV-cured coatings for aircraft |
US8623220B2 (en) | 2012-01-01 | 2014-01-07 | King Abdulaziz City for Science and Technology (KACST) | Synthesis of copper oxide-doped zinc-oxide nanoparticles and their use |
US20140183141A1 (en) | 2012-12-31 | 2014-07-03 | Ms. Deepika Saraswathy Kurup | Photocatalytic Composition for Water Purification |
CN104874466A (zh) | 2015-05-10 | 2015-09-02 | 德清县东旭合金钢铸造有限公司 | 一种制砂机的下料斗 |
CN104877446B (zh) * | 2015-06-19 | 2017-09-08 | 天津市合成材料工业研究所有限公司 | 一种紫外‑热双重固化玻璃油墨及其制备方法 |
JP6864420B2 (ja) * | 2015-12-24 | 2021-04-28 | 大日本塗料株式会社 | 建築板及び塗料組成物 |
EP4011988A1 (en) | 2016-04-11 | 2022-06-15 | Sun Chemical Corporation | Process for electron beam curable inkjet formulations |
AU2017253480B2 (en) | 2016-04-21 | 2021-01-07 | Flint Group Sweden Ab | Radiation curable ink formulation |
WO2019216961A1 (en) * | 2018-05-10 | 2019-11-14 | Sun Chemical Corporation | Actinic radiation curable compositions including semiconductor metal oxide materials |
-
2019
- 2019-01-09 WO PCT/US2019/012849 patent/WO2019216961A1/en active Application Filing
- 2019-01-09 EP EP19800206.5A patent/EP3814023A4/en active Pending
- 2019-01-09 US US17/048,472 patent/US11254830B2/en active Active
- 2019-01-09 BR BR112020022464-2A patent/BR112020022464A2/pt unknown
- 2019-01-09 JP JP2020561889A patent/JP7499187B2/ja active Active
-
2022
- 2022-02-15 JP JP2022021172A patent/JP2022060346A/ja active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3041172A (en) | 1958-12-30 | 1962-06-26 | Gen Aniline & Film Corp | Photopolymerization of vinyl monomers with metal oxides as catalysts |
US3346383A (en) | 1960-11-23 | 1967-10-10 | Eastman Kodak Co | Image reproduction processes utilizing photopolymerization of vinyl monomer compositions comprising a metallic sulfide compound |
US3147119A (en) | 1962-05-18 | 1964-09-01 | Gen Aniline & Film Corp | Photopolymerization of vinyl monomers with metal oxides as catalysts |
US4257915A (en) | 1979-07-23 | 1981-03-24 | E. I. Du Pont De Nemours And Company | Photopolymer initiator system containing a semiconductor, a reducing agent and an oxidizing agent |
JP2006219855A (ja) | 2005-02-09 | 2006-08-24 | Marutama Sangyo Kk | 木質系床材とその製造法 |
JP5234714B2 (ja) | 2007-02-21 | 2013-07-10 | 三菱重工印刷紙工機械株式会社 | 印刷機 |
Also Published As
Publication number | Publication date |
---|---|
US11254830B2 (en) | 2022-02-22 |
JP2022060346A (ja) | 2022-04-14 |
JP2021517200A (ja) | 2021-07-15 |
EP3814023A4 (en) | 2021-07-21 |
EP3814023A1 (en) | 2021-05-05 |
US20210087421A1 (en) | 2021-03-25 |
BR112020022464A2 (pt) | 2021-02-09 |
WO2019216961A1 (en) | 2019-11-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP7499187B2 (ja) | 半導体金属酸化物材料を含む化学線硬化性組成物 | |
EP3442720B1 (en) | Process for electron beam curable inkjet formulations | |
JP7389035B2 (ja) | 第iv族金属キレート、ならびに放射線硬化性インクおよびコーティング組成物におけるその使用 | |
EP3353244A1 (en) | Polymeric aminoacrylates | |
EP4150019B1 (en) | Adhesion promoters for uv flexographic inks and coatings | |
US11236243B2 (en) | Low migration energy curable inks | |
JP7236262B2 (ja) | 印刷物の製造方法 | |
JP2024086743A (ja) | 半導体金属酸化物材料を含む化学線硬化性組成物 | |
US11993721B2 (en) | LED energy curable ink compositions | |
US11976203B2 (en) | Energy curable inks and coatings with peroxides | |
JP7277674B2 (ja) | 活性エネルギー線硬化性組成物、及び艶消しコーティング膜の製造方法 | |
WO2024091386A1 (en) | Energy-curable flexographic black laminating ink | |
JP2023125337A (ja) | 樹脂組成物、硬化物、物品及び硬化物の製造方法 | |
JP2023146160A (ja) | 活性エネルギー線硬化型オフセット印刷インキ、これを用いた印刷物、及び印刷物の製造方法 | |
WO2023141118A1 (en) | Uv curable inks and coatings | |
JP2016011412A (ja) | 活性エネルギー線硬化型インキの多色セット | |
WO2024020037A1 (en) | Viscosity modifiers for energy curable inks | |
JP2021195468A (ja) | 平版オフセット印刷用活性エネルギー線硬化型インキ及びインキ硬化物の製造方法 | |
JP2022093793A (ja) | 活性エネルギー線硬化型平版印刷インキ組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A529 | Written submission of copy of amendment under article 34 pct |
Free format text: JAPANESE INTERMEDIATE CODE: A529 Effective date: 20201111 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20201111 |
|
A871 | Explanation of circumstances concerning accelerated examination |
Free format text: JAPANESE INTERMEDIATE CODE: A871 Effective date: 20201111 |
|
A975 | Report on accelerated examination |
Free format text: JAPANESE INTERMEDIATE CODE: A971005 Effective date: 20210401 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20210421 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20210721 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20210921 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20211019 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20220215 |
|
C60 | Trial request (containing other claim documents, opposition documents) |
Free format text: JAPANESE INTERMEDIATE CODE: C60 Effective date: 20220215 |
|
C11 | Written invitation by the commissioner to file amendments |
Free format text: JAPANESE INTERMEDIATE CODE: C11 Effective date: 20220224 |
|
A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20220404 |
|
C21 | Notice of transfer of a case for reconsideration by examiners before appeal proceedings |
Free format text: JAPANESE INTERMEDIATE CODE: C21 Effective date: 20220405 |
|
A912 | Re-examination (zenchi) completed and case transferred to appeal board |
Free format text: JAPANESE INTERMEDIATE CODE: A912 Effective date: 20220422 |
|
C211 | Notice of termination of reconsideration by examiners before appeal proceedings |
Free format text: JAPANESE INTERMEDIATE CODE: C211 Effective date: 20220426 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20240228 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20240327 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20240603 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 7499187 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |