JPS5845248A - Coating composition - Google Patents
Coating compositionInfo
- Publication number
- JPS5845248A JPS5845248A JP14420581A JP14420581A JPS5845248A JP S5845248 A JPS5845248 A JP S5845248A JP 14420581 A JP14420581 A JP 14420581A JP 14420581 A JP14420581 A JP 14420581A JP S5845248 A JPS5845248 A JP S5845248A
- Authority
- JP
- Japan
- Prior art keywords
- coating
- photographic
- layer
- coating composition
- present
- 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.)
- Granted
Links
- 239000008199 coating composition Substances 0.000 title claims description 27
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 33
- 239000000203 mixture Substances 0.000 claims description 21
- 239000000377 silicon dioxide Substances 0.000 claims description 11
- 239000008119 colloidal silica Substances 0.000 claims description 10
- 239000010410 layer Substances 0.000 description 30
- 238000000576 coating method Methods 0.000 description 29
- 239000011248 coating agent Substances 0.000 description 24
- 239000000463 material Substances 0.000 description 24
- -1 sulfate alkali metal salts Chemical class 0.000 description 22
- 239000011247 coating layer Substances 0.000 description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 14
- 239000000178 monomer Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 10
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 8
- 239000004332 silver Substances 0.000 description 8
- 229910052709 silver Inorganic materials 0.000 description 8
- 229920002554 vinyl polymer Polymers 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 230000002209 hydrophobic effect Effects 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 239000002216 antistatic agent Substances 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000001913 cellulose Substances 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 5
- 239000000470 constituent Substances 0.000 description 5
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 5
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000006224 matting agent Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229920003169 water-soluble polymer Polymers 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 108010010803 Gelatin Proteins 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 208000028659 discharge Diseases 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000002612 dispersion medium Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 150000002484 inorganic compounds Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical class COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 101001133605 Homo sapiens Parkin coregulated gene protein Proteins 0.000 description 1
- SPAGIJMPHSUYSE-UHFFFAOYSA-N Magnesium peroxide Chemical compound [Mg+2].[O-][O-] SPAGIJMPHSUYSE-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 240000000220 Panda oleosa Species 0.000 description 1
- 235000016496 Panda oleosa Nutrition 0.000 description 1
- 102100034314 Parkin coregulated gene protein Human genes 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000002947 alkylene 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
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- UHHXUPJJDHEMGX-UHFFFAOYSA-K azanium;manganese(3+);phosphonato phosphate Chemical compound [NH4+].[Mn+3].[O-]P([O-])(=O)OP([O-])([O-])=O UHHXUPJJDHEMGX-UHFFFAOYSA-K 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- WXCZUWHSJWOTRV-UHFFFAOYSA-N but-1-ene;ethene Chemical compound C=C.CCC=C WXCZUWHSJWOTRV-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- HRBZRZSCMANEHQ-UHFFFAOYSA-L calcium;hexadecanoate Chemical compound [Ca+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O HRBZRZSCMANEHQ-UHFFFAOYSA-L 0.000 description 1
- 229920006319 cationized starch Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 1
- MYRTYDVEIRVNKP-UHFFFAOYSA-N divinylbenzene Substances C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- RLJSXMVTLMHXJS-UHFFFAOYSA-M sodium;4-decylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 RLJSXMVTLMHXJS-UHFFFAOYSA-M 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は新規な塗布組成物に関し、詳しくは塗液の安定
性が改良された帯電防止性の塗布組成物に関するものf
ある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel coating composition, and more particularly to an antistatic coating composition with improved coating liquid stability.
be.
ところf、絶縁性の支持体は、該支持体上に静電気が不
所望の形f蓄積するということがヒれまf問題となって
いた・かかる絶縁性の支持体としては、Iリエチレンテ
レ7タレートフイルム、)9酢酸セルロ一スフイルム%
/IJスチレンフィルムslリカー−ネートフィルムな
どのフィルム、紙を基質としてその両面をフィルム形成
能ある樹脂、多くは4リオレフイン樹脂で被覆した樹脂
被覆紙などの疎水性支持体がよく知られている。さらに
、絶縁性の支持体上に帯電防止性層を設けることにより
て静電気が防止されるということも全知となりている。However, insulating supports have been problematic in that static electricity accumulates in an undesired manner on the supports. tallate film,) 9 acetic acid cellulose film%
Hydrophobic supports are well known, such as films such as /IJ styrene film sl recarbonate film, and resin-coated paper made of a paper substrate coated on both sides with a film-forming resin, often a 4-lyolefin resin. Furthermore, it is well known that static electricity can be prevented by providing an antistatic layer on an insulating support.
しかしながら、支持体上に塗布することが1きるような
帯電防止性の組成物を調製可能であるというものの、帯
電防止性とその他の望ましい物性とを組み会わせること
は非常に困難なことfあ。However, although it is possible to prepare antistatic compositions that can be coated onto a support, it can be very difficult to combine antistatic properties with other desirable physical properties. .
る。Ru.
さらに、疎水性支持体と諒支持体上に設けられた写真構
成層(例えば、写真乳剤層、保護層、下引層、Aツクコ
ート層などおよびそれらの組み合わせ層)とから成る写
真材料に適した帯電防止組成物を調製することは、その
ような材料に要求されている物性が厳密であるために、
一層複雑とな9ている。絶縁性の支持体から成る写真材
料に適し九有利な帯電防止組成物としては1例えばスチ
レンなどの炭素a4以上のエチシン系不飽和共重合性単
量体と無水マレイン酸との共重合によって得られる水溶
性高分子化合物と:I四イP状シリカおよび硬化剤を主
成分とする塗布層が知られている。具体的には1例えば
特開昭55−32009号などに記載がある。Furthermore, it is suitable for a photographic material consisting of a hydrophobic support and a photographic constituent layer provided on the support (for example, a photographic emulsion layer, a protective layer, a subbing layer, an Atsuk coat layer, etc., and a combination layer thereof). Preparing antistatic compositions is difficult due to the rigorous physical properties required of such materials.
9 It has become even more complex. An advantageous antistatic composition suitable for photographic materials comprising an insulating support is one obtained by copolymerizing an ethicine-based unsaturated copolymerizable monomer having carbon a4 or more, such as styrene, with maleic anhydride. A coating layer containing a water-soluble polymer compound, P-type silica, and a curing agent as main components is known. Specifically, there is a description in JP-A-55-32009, for example.
この塗布層は、以下の様な長所を有するため。This coating layer has the following advantages.
かなp優れ喪ものである。第一に、単一の塗布層である
丸め、塗布工程が簡単である。第二に疎水性支持体に十
分に接着して硬化する塗布層であるため、該塗布層を具
えた疎水性支持体から成る写真材料は、その現偉処理中
に膜剥れなどの問題を起すことがない。第三に、優えた
帯電防止性の塗布層であるため、該塗布層を具えた疎水
性支持体から成る写真材料は、静電気の著積による問題
を起すことがない。第四に、写真的悪影響を与えない塗
布層である。以上の様な点1、この塗布層はかなシ優れ
ているものの、更に重大な問題点を有していることが明
らかとなった。Kana p is an excellent mourning thing. First, the rolling and coating process, which is a single coating layer, is simple. Second, since the coating layer adheres well to the hydrophobic support and hardens, photographic materials made of hydrophobic supports equipped with the coating layer do not suffer from problems such as film peeling during processing. I never wake up. Thirdly, because the coating layer has excellent antistatic properties, the photographic material comprising the hydrophobic support provided with the coating layer does not suffer from problems due to the accumulation of static electricity. Fourthly, it is a coating layer that does not have any adverse photographic effects. Point 1 as mentioned above: Although this coating layer has excellent properties, it has become clear that it has a more serious problem.
即ち、絶縁性の支持体上に塗布することが1きるような
帯電防止性の組成物に、単一層塗布で帯電防止性、11
着性、写真適性、その他カール肪止性などの多目的な機
能を持たせようと、しばしば、それもq#にカルIン差
基を有する親水性d9マーとコロイド状シリカとが存在
している時に、塗布液の安定性が悪くなり、塗布液成分
の沈降、分離、凝集などが起る傾向があるという重大な
問題がある。このため、塗布液の安定性の優れた多目的
機能を持つ帯電防止性の塗布組成物の開発が望まれてい
た。That is, by applying a single layer to an antistatic composition that can be coated on an insulating support, antistatic properties can be obtained.
In order to provide multi-purpose functions such as adhesion, photographic suitability, and other curl-fat retention properties, hydrophilic d9-mer and colloidal silica, which also have a cal-I group at q#, are often present. At times, there is a serious problem in that the stability of the coating solution deteriorates and coating solution components tend to settle, separate, agglomerate, etc. For this reason, it has been desired to develop an antistatic coating composition with excellent coating liquid stability and multipurpose functions.
従うて1本発明の目的は、第一に、塗液の安定性の優れ
九帯電防止性の塗布組成物を提供することである。第二
に、塗液の安定性が良く・しかも単一層で多目的機能を
持つ帯電防止性の写真構成層用塗布組成物を提供し、そ
れ故疎水性支持体から成る優れた写真材料の製造を可能
にすることである。本発明のその他の目的、特徴及び利
点等杜、以下の明細書の記載から理解されよう。Accordingly, an object of the present invention is, first, to provide a coating composition with excellent stability and antistatic properties. Second, it provides an antistatic coating composition for photographic constituent layers that has good coating stability and has multipurpose functions in a single layer, and therefore facilitates the production of superior photographic materials comprising hydrophobic supports. It is about making it possible. Other objects, features, and advantages of the present invention will be apparent from the following description.
本発明者らが鋭意検討の結果1本発明の目的は、(@)
カル−キシル基を有する親水性ポリY −ト<b>コロ
イド状シリカと(C)/す♂ニルピロリrンとから構成
されており、かつ(J):=*aイP状シリカ:(C)
ポリ−ニルぜロリrンの構成比率が1:O,OO1〜l
:o、150である塗布組成物によって達成されること
がわかった。更に述べれば、本発明において、(b)コ
ロイド状シリカ:(c) $すtxs、ピ四りPンの構
成比率がl:o、001以下1あれば1本発明の効果は
得られないし。As a result of intensive studies by the inventors, the purpose of the present invention is (@)
It is composed of a hydrophilic polyY-t<b>colloidal silica having a car-xyl group and (C)/snylpyrroline, and (J):=*a-P-type silica: (C )
The composition ratio of poly-nylzerorin is 1:O, OO1~l
: o, 150. To be more specific, in the present invention, if the composition ratio of (b) colloidal silica to (c) $txs, P4P is l:o, 1 or less than 001, the effects of the present invention cannot be obtained.
ま九構成比率が1:O,150以上−r@あれば、塗液
の安定性が再び悪くなり、本発明の効果は得られない。If the composition ratio is 1:O, 150 or more -r@, the stability of the coating liquid deteriorates again, and the effects of the present invention cannot be obtained.
本発明の実施に用いられるカルーiシ基を有する親水性
4リマーとしては・各種のものを使用することが1きる
。特に、炭素教養以上のエチレン系不飽和共重合性単量
体と、無水マレイン酸との共重合によって得られる水溶
性高分子化合物もしくはその塩が有利に用いられる。ま
た、ゼラチンおよびゼラチン誘導体、カル−キシル基を
有するIリアクリルアミド、カル−キシル基を有する一
すCニルアルコールなど、更に炭素教養以上のエチレン
系不飽和共重合性単量体と無水マレイン酸との共重合物
と?す♂ニルアル;−ルとの水溶性加工物もしくはその
塩など各種のものを使用することができる。As the hydrophilic 4-limer having a carousel group used in the practice of the present invention, various types can be used. In particular, a water-soluble polymer compound or a salt thereof obtained by copolymerizing an ethylenically unsaturated copolymerizable monomer with a carbon content or higher and maleic anhydride is advantageously used. In addition, gelatin and gelatin derivatives, I-lyacrylamide having a carxyl group, mono-C-nyl alcohol having a carxyl group, and ethylenically unsaturated copolymerizable monomers with a carbon level or higher and maleic anhydride. With a copolymer of? Various kinds of products such as water-soluble processed products of sodium chloride or salts thereof can be used.
本発明の実施に特に有利に用いられる炭素教養以上のエ
チレン系不飽和共重合性単量体と無水マレイン酸との共
重合によって得られる水溶性高分子化合一もしくはその
塩は炭素教養以上のα−オレフィン、アルキル−エルエ
ーテル。A water-soluble polymer compound or a salt thereof obtained by copolymerizing an ethylenically unsaturated copolymerizable monomer with a carbon content or higher and maleic anhydride, which is particularly advantageously used in carrying out the present invention, has a carbon content of α or higher. -Olefins, alkyl-elethers.
スチレンの如きエチレン系不飽和共重合性単量体と無水
マレイン酸との共重合体を必要に応じて水酸化ナトリウ
ム、水酸化カリウム、アンモニア等のアルカリと共に加
水分解して得られる。It is obtained by hydrolyzing a copolymer of an ethylenically unsaturated copolymerizable monomer such as styrene and maleic anhydride, optionally with an alkali such as sodium hydroxide, potassium hydroxide, or ammonia.
エチレン系不飽和共重合性単量体と無水マレイン酸との
共重合体およびその製造法については米国特許第2,0
47,398号等に記載がある。A copolymer of an ethylenically unsaturated copolymerizable monomer and maleic anhydride and a method for producing the same are disclosed in U.S. Patent No. 2,0
It is described in No. 47,398, etc.
好ましいエチレン系不飽和共重合性単量体としては、炭
素教養以上のα−オレツイン、アルキルぜエルエーテル
、スチレン、更に好tL<a炭素数5以上のα−オレフ
ィン、炭素数3以上のアルキルを有するアルキル−ニル
エーテル、スチレンがある。また、炭素数4以上のエチ
レン系不飽和共重合性単量体と無水マレイン酸共重合体
の分子量としては、2千〜15万のものが好ましい。炭
素数4以上のエチレン系不飽和共重合性単量体と無水マ
レイン酸との共重合によりて得られる水溶性−高分子化
合物もしくはその壇の具体例としては、例えば、インブ
チレン、1−ペンfン、ブチルビニルエーテルt+はス
チレンと無水マレイン酸との共重合体を水酸ナトリウム
、水酸化カリウム等のアルカリと共に加水分解して得ら
れる溶液の−が6.0〜9.0″′I4ある反応生成物
などがあげられる。Preferred ethylenically unsaturated copolymerizable monomers include α-oletuin, alkyl gel ether, styrene, and more preferably tL<a α-olefin having 5 or more carbon atoms, and alkyl having 3 or more carbon atoms. There is an alkyl-nyl ether with styrene. Further, the molecular weight of the ethylenically unsaturated copolymerizable monomer having 4 or more carbon atoms and the maleic anhydride copolymer is preferably 2,000 to 150,000. Specific examples of water-soluble polymeric compounds obtained by copolymerizing an ethylenically unsaturated copolymerizable monomer having 4 or more carbon atoms with maleic anhydride or their bases include inbutylene, 1-pene, etc. Butyl vinyl ether t+ is a solution obtained by hydrolyzing a copolymer of styrene and maleic anhydride with an alkali such as sodium hydroxide or potassium hydroxide. Examples include reaction products.
本発明の実施に用いられるコロイド状シリカとは主とし
て水を分散媒として無水珪酸(810禦)を超微粒子″
e(平均粒子径6〜60mμ)水中に分散せしめたコロ
イド溶液→ある。また、分散媒は一般に水″eあるがメ
タノール等を用いる場合もある。またコロイド溶液中に
、コロイド安定剤などの目的でアルカリ成分を含有する
。九とえばNαOHや他K NHs、ホルムアtP1モ
ルホリン等を含む場合もある。本発明に好ましく用いら
れる′3四イP状シリカの市販品゛としては、日量化学
■製スノーテックスがある。The colloidal silica used in the practice of the present invention is mainly composed of ultrafine particles of silicic anhydride (810) using water as a dispersion medium.
e (average particle size 6-60 mμ) A colloidal solution dispersed in water. In addition, the dispersion medium is generally water, but methanol or the like may be used in some cases.Also, the colloidal solution contains an alkaline component for the purpose of colloid stabilizer. A commercially available P-type silica preferably used in the present invention is Snowtex manufactured by Nichichi Kagaku.
本発明の実施に用いられるぼりビニル♂ロリPy拡各種
の分子量および粘度のものを使用し得るが、その分子量
が8000〜40万程度のものが有用である。IIIす
♂エル♂ロリPンの市販品として杜、ガフ(G、A、F
)社製階に一1a PVP K−30,PVP K−6
0,PVP K−90がある。Although various molecular weights and viscosities of the vinyl ♂ and viscosity used in the practice of the present invention can be used, those having a molecular weight of about 8,000 to 400,000 are useful. Mori, Gaff (G, A, F
) PVP K-30, PVP K-6
0, PVP K-90 is available.
本発明において−りtエルピロリPンを塗布組成物中に
含有せしめる好ましい実施態様としては、それぞれ所定
量のコロイド状シリカの水溶液と4リビエル♂四りPン
の水溶液とを予め混合し友後、該混合液をカル−キシル
基を方する親水性がり!−の水溶液中に添加するが好ま
しいが1本発明は勿論これらの実施態様に限定されるも
のではない。In a preferred embodiment of the present invention, a preferred embodiment of incorporating L pylori P into the coating composition is to mix predetermined amounts of an aqueous solution of colloidal silica and an aqueous solution of L pylori P in pre-mixing, The mixture has hydrophilic properties that promote carxyl groups! Although it is preferable to add it to an aqueous solution of -1, the present invention is of course not limited to these embodiments.
本発明の実施に用いられる各成分の塗布組成物中の濃度
あるいは使用量は、塗布方法、帯電防止性などの必要と
される諸物性、塗布組成物中への添加剤などによって実
質的に決定されるもの1あり、特に限定されるものでな
いが、(、)(b)(c)各成分の総量固形分濃度とし
て、1.0重量S〜10重−チ範囲が有用1ある。また
、塗布組成物の−は9.0以下、好ましくは7.0以下
にする9が望ましい。The concentration or usage amount of each component in the coating composition used in carrying out the present invention is substantially determined by the coating method, required physical properties such as antistatic properties, additives in the coating composition, etc. Although not particularly limited, there is a useful range of the total solid content concentration of each component (,), (b), and (c) from 1.0 weight S to 10 weight H. Further, it is desirable that the - of the coating composition be 9.0 or less, preferably 7.0 or less.
本発明における帯電防止性の塗布組成物中に別種の帯電
防止剤を含有せしめて、該塗布組成物の帯電防止能を一
層顕著に発揮せしめるのが好ましい。好ましい帯電防止
剤としては、例え種名)などの硫酸繊維素アルカリ金属
塩、オリ♂−2(6川製紙社製の商標名)、ケ考スタツ
)6120(三洋化成工業社製の商標名)などの/9ス
チレンスルフォン酸のアルカリ塩、ポリアクリル酸ナト
リウム(例えば、ぼりアクリル酸、ポリメタアクリル酸
、ポリ−α−エチルアクリル酸のナトリウム塩などつ、
4リアクリル酸カリウム、アクリル酸とアクリル酸メチ
ル共重合体のナトリウム塩などの重合せるアクリル酸類
およびアクリル酸共重合体のアルカリ塩などがある。こ
れらの帯電防止剤の使用量としては1本発明における塗
布組成物の構成(例えば、構成/9マーの種類、支持体
\の塗布量。It is preferable to include another type of antistatic agent in the antistatic coating composition of the present invention so that the antistatic ability of the coating composition can be more markedly exhibited. Preferred antistatic agents include cellulose sulfate alkali metal salts such as (species name), Ori♂-2 (trade name, manufactured by Six River Paper Co., Ltd.), Keko Stats) 6120 (trade name, manufactured by Sanyo Chemical Industries, Ltd.) /9 Alkaline salts of styrene sulfonic acid, sodium polyacrylates (e.g., sodium salts of polyacrylic acid, polymethacrylic acid, poly-alpha-ethyl acrylic acid, etc.),
Examples include alkali salts of polymerizable acrylic acids and acrylic acid copolymers, such as potassium 4-lyacrylate and sodium salts of acrylic acid and methyl acrylate copolymers. The amount of these antistatic agents to be used depends on the composition of the coating composition in the present invention (for example, composition/type of 9mer, coating amount of support).
塗布組成物の−など)、帯電防止剤の種類などによりて
も異るが、支持体への塗布量が0.01Vwl〜3体の
範囲になる量が好ましい・本発明における塗布組成物中
には1本発明における水溶性Iリマーと共に種々のIリ
マー゛を本発明の効果を損わない範囲1併用して含有せ
しめることができる。これらの−リマーとしてハ1例え
ば4リピニルアルコール、4リアクリルアfP、澱粉ま
たはこれらの誘導体、セルロース誘導体などがある。Although it varies depending on the coating composition (e.g.) and the type of antistatic agent, it is preferable that the coating amount on the support is in the range of 0.01 Vwl to 3 Vwl. In addition to the water-soluble I remer used in the present invention, various I remers may be contained in combination within a range that does not impair the effects of the present invention. Examples of these remers include 4-lipinyl alcohol, 4-lyacrylic acid fP, starch or derivatives thereof, and cellulose derivatives.
また1本発明における塗布組成物中には、各種のマット
剤を含有せしめることができる。マット剤はこれを適用
した本発明の組成物から成る塗布層を有する支持体同志
あるいは写真材料同志またはヒれらと接触する物体間と
の粘着性を排除するのに有効fある。これらのマット剤
としては水不溶性の無機または有機化合物の微粒+1、
粒子径が0.2μから6μ(%に0.5〜3a)t″r
!のものが有用である・無機化合物の例としては、二酸
化珪素、二酸化チタン、二酸化マグネシウム、二酸化ア
ルζニウム、硫酸ノンリウム、炭酸カルシウム、カオリ
ナイトクレー、ガラス粉などを好ましく用いる仁とが1
きる。Furthermore, the coating composition of the present invention may contain various matting agents. The matting agent is effective in eliminating adhesion between supports having coating layers made of the composition of the present invention, between photographic materials, or between objects that come into contact with the fins. These matting agents include water-insoluble inorganic or organic compound fine particles +1;
Particle size is 0.2μ to 6μ (0.5 to 3a in %)t″r
! Examples of inorganic compounds include silicon dioxide, titanium dioxide, magnesium dioxide, aluminum ζium dioxide, nonlium sulfate, calcium carbonate, kaolinite clay, and glass powder.
Wear.
有機化合物の例としては、水分散性ビニル重合体の例と
して、−リアクリル酸メチル、Iリメタアクリル酸メチ
ル、/リスチνン、スチレンとジビニルベンぜン共重合
体、−リ♂ニルアセテート、Iリエチレンカーゼネート
、/リアトラフルオロエチレンなど・セル四−ス誘導体
の例、!=して、)+ルセルロース、エチルセルロース
など、澱粉粒なεを好ましく用いることが1きる。これ
らのマット剤は必要に応じて異る種類の物質を併用する
ことができる。Examples of organic compounds include water-dispersible vinyl polymers such as methyl lyacrylate, methyl methacrylate, lystine, styrene and divinylbenzene copolymer, lysinyl acetate, I Examples of cellulose derivatives such as lyethylene carzenate and lyatrafluoroethylene! It is preferable to use starch grains such as cellulose and ethyl cellulose. These matting agents can be used in combination with different types of substances, if necessary.
本発明における塗布組成物中には、各種の添加剤を含有
せしめることが1きる。硬膜剤として、特開昭55−6
9139に記載もしくは例示の分子中の2個以上のエチ
レンイ建ノ基また線ダリジルエーテル基を有する硬膜剤
など、界面活性剤として、アル中、11/−(ンぜンス
ルフォン酸塩、スル7オーハク酸エステル塩などのアニ
オン界面活性剤、?4二ン、アルキレンオキサイP化合
物等のノニオン界面活性剤、ア々)酸114* 7 t
/スルフォン酸類、アミノアルー−ルのエステル類等
の両性界面活性剤、特開昭5O−G)9529号に例示
の弗素系界面活性剤など螢光増白剤として、骨分rI3
4δ−2養068号特開昭54−94318号などに記
載もしくは例示の化合物、膜物性改良剤として、アクリ
ル酸エステル、−二ルエステル等ト他のエチレン基を持
つ単量体との共重合体から成るラテックス、J)エン系
単量体の共重合体から成るラテックス、これらのカルが
キシ変性ラテックスなどの添加剤を単独ま九は組み合わ
せて含有せしめることができる。The coating composition of the present invention may contain various additives. As a hardening agent, JP-A-55-6
As a surfactant, hardeners having two or more ethylene groups or linear dalidyl ether groups in molecules described or exemplified in No. 9139, Anionic surfactants such as ester salts, nonionic surfactants such as ?4-2, alkylene oxy-P compounds, az) acids 114*7t
Ampholytic surfactants such as esters of /sulfonic acids and aminoalols, fluorine-based surfactants as exemplified in JP-A No. 50-G) 9529, etc., as fluorescent brighteners, bone rI3
Compounds described or exemplified in 4δ-2 Yo068, JP-A-54-94318, etc., and copolymers with other ethylene group-containing monomers such as acrylic esters and -dyl esters as film property improvers. (J) a latex consisting of a copolymer of an ene monomer, a latex consisting of a copolymer of ene-based monomers, and a latex modified with xylene.
本発明の塗布組成物は種々の塗布方法で支持体の片面あ
るいは両面に塗布することが!きる。The coating composition of the present invention can be applied to one or both sides of a support using various coating methods! Wear.
その際、支持体面にコ四す放電、グロー放電。At that time, a glow discharge occurs on the surface of the support.
その他の電子衝撃、火炎処理、粗面化、紫外線照射、オ
ゾン酸化などの表面活性化処理を施した後に塗布するの
が好ましい。また、塗布は、スクイズコーター、ノセー
コーター、フレーPコーター、グラビアコーター、エア
ナイフコーター、スライドホッノぐ−コーターなどおよ
びそれらの組み合わせ方式により行うことが1きる。It is preferable to apply the coating after performing other surface activation treatments such as electron impact, flame treatment, surface roughening, ultraviolet irradiation, and ozone oxidation. The coating can be performed using a squeeze coater, a spray coater, a flake coater, a gravure coater, an air knife coater, a slide hook coater, or a combination thereof.
塗布後の乾燥は熱風、赤外線、加熱r2イヤー、マイク
ロ波など各種の方法により行うことが1きる。Drying after application can be carried out by various methods such as hot air, infrared rays, heated R2 ears, and microwaves.
また、本発明における塗布組成物を支持体に塗布する際
の組成物各成分の塗布量として、カルIキシル蓬を有す
る親水性ポリマーの塗布量は、0.01ル冒〜101/
v?の範囲が有用fあるが、好ましくはαl&曾〜凸、
OIi貨の範囲1ある。また、コロイP状シリカの塗布
量は、 0.0111/rrl〜1011/lriの範
囲が有用fあるが、好ましくはO,l 11/11〜6
.0シqの範囲1ある。更に・。Furthermore, when applying the coating composition of the present invention to a support, the coating amount of the hydrophilic polymer having Cal I xyl ester is 0.01 to 101/
v? There is a useful range f, but preferably αl & so ~ convex,
There is a range of OIi coins. The coating amount of colloidal P-type silica is usefully in the range of 0.0111/rrl to 1011/lri, but preferably O,l 11/11 to 6
.. There is a range of 0 sq. Furthermore...
4すビニルぜロリ?ンはコロイP律シリカの置に見合り
た適正量が塗布される。4S Vinyl Loli? The coating is applied in an appropriate amount commensurate with the location of the Colloy P silica.
iた1本発明に係る疎水性支持体としては各種のものが
使用される0例えば、がリゾロ♂レン、/リスチレンの
如き合成紙、セルロースアセテート、セル■−スナイト
レート、ポリエチレンテレフタレート、ぼりビニルアセ
テート、4リスチレン、4リアf 1’、 /リカーー
ネートの如きフィルム、を九、α−オレフィンポリマー
特に4リエチレン、−リゾ−ピレン、エチレン−ブテン
コー9▼−等炭素原子2〜10個のα−オレフインーリ
マーをう電ネートした紙などが有利に用いられる。これ
らの熱可塑性樹脂フィルムま丸線4リオレフィン樹脂層
中には、酸化チタン、酸化亜鉛、メルク、炭酸カルシウ
ムなどの白色調料、:2ノルドデルー1紺青、群青、セ
リアンツルー、フタ四シアニンブルーなどのブルーの顔
料や染料、コノ臂ルトノ々イオレット、ファストノ臂イ
オレvト、マンガン紫などのマぜン夕の顔料や染料、ス
テアリン酸亜鉛、ステアリン酸カルシウム、パルミチン
酸カルシウムなどの脂肪酸金属塩の分散剤1通常、樹脂
に混合される安定剤、酸化防止剤、帯電防止剤。Various types of hydrophobic supports can be used in the present invention, such as synthetic paper such as lysolo♂lene and lystyrene, cellulose acetate, cellulose nitrate, polyethylene terephthalate, and vinyl paper. Films such as acetate, 4-lystyrene, 4-lystyrene, 4-lycarnates, 9-, α-olefin polymers, especially 4-lystyrene, lyso-pyrene, ethylene-butene, etc., containing 2 to 10 carbon atoms. Advantageously, paper or the like is used, which is electrified with In-Limer. These thermoplastic resin films, round wires, 4 lyolefin resin layers contain white additives such as titanium oxide, zinc oxide, Merck, and calcium carbonate; Pigments and dyes such as violet violet, fast iolet, manganese violet, etc., dispersants of fatty acid metal salts such as zinc stearate, calcium stearate, and calcium palmitate 1. , stabilizers, antioxidants, and antistatic agents that are mixed into resins.
可塑剤、滑剤、螢光剤、紫外線吸収剤などの添加剤を加
えてもよい。Additives such as plasticizers, lubricants, fluorescent agents, and ultraviolet absorbers may also be added.
本発明の塗布組成物は、これを写真構成層に適用1て写
真材料の調製に使用するのが有利1ある。かかる写真構
成層としては、写真乳剤層、保護層、下引層、乳剤層と
乳剤層との間の中間層、ハレーシ嘗ン防止層もしくはフ
ィルタ一層、紫外線吸収剤を含む紫轟収層、銀塩拡散転
写法用の受偉層、支持体の裏面、即ち写真乳剤層とは反
対側の支持体面上に設けられるノ9ツクコート層などお
よびそれらの組み合わせ層が包含されるが、本発明の塗
布組成物は、特に/9ツクコート層および下引層に適用
するのが有利1ある。ま九1本発明の塗布組成物が適用
fきる写真材料としては、錯塩写真材料、ジアゾタイプ
写真材料、気泡−画儂形成性写真材料、光重合性写真材
料壜どの各種のものを包含するが、銀塩写真材料、特に
ハロゲン化銀写真材料に適用するのが有用である。更に
1本発明が有効なハロゲン化銀写真材料としては、ハロ
ゲン化銀白黒写真材料、ハロゲノ化銀カッー写真材料、
多層ハ四ゲン化銀カラー写真材料、拡散転写法用写真要
素、直接ポジ盟ハEl/ン化銀写真材料。The coating composition of the invention is advantageously used in the preparation of photographic materials by applying it to photographic constituent layers. Such photographic constituent layers include a photographic emulsion layer, a protective layer, a subbing layer, an intermediate layer between emulsion layers, an anti-halation layer or a filter layer, a UV absorption layer containing an ultraviolet absorber, a silver Coatings of the present invention include coating layers for salt diffusion transfer, coating layers provided on the back side of the support, that is, the side of the support opposite to the photographic emulsion layer, and combinations thereof. The composition is advantageously applied in particular to coat layers and subbing layers. Photographic materials to which the coating composition of the present invention can be applied include various types of photographic materials such as complex salt photographic materials, diazo type photographic materials, bubble-forming photographic materials, and photopolymerizable photographic material bottles. It is useful to apply to silver salt photographic materials, especially silver halide photographic materials. Furthermore, silver halide photographic materials to which the present invention is effective include silver halide black and white photographic materials, silver halide black photographic materials,
Multilayer silver tetragenide color photographic materials, photographic elements for diffusion transfer methods, direct positive silver chloride photographic materials.
一般印画紙用、写植印画紙用、複写印画紙用。For general photographic paper, typesetting photographic paper, and copy photographic paper.
印刷材料用など種類、用途線特に制限されるものfはな
い、また、かかるハロゲン化銀写真材料の写真構成層中
には、ハイポなどの化学増感剤、金塩、白金などの貴金
属増感剤、ヘキサハロゲノイリジウム(至)錯体、ヘキ
サハロゲノロジウム(至)錯体などの硬調化剤、核酸分
解物、特開昭50−14792δ号、同第51−107
129号に記載鬼しくけ例示のメルカゾト複素環化金物
、色増感剤、安定剤、カゾリ防止剤、カラー写真用カゾ
ラー、硬膜剤、非拡散性シアル中ルジヒドロキシ4ンぜ
ン化合物、ハイドロキノン、メチルハイP■キノン、フ
ェニドンなどのハロゲン化鋏現偉剤、塗布助剤、またカ
ブラセ剤、直接?ジ用染料などの直接ポジ写真乳剤用添
加剤、色素現像薬、その細鉱散転写法用写真要素の物理
現像核などを含有せしめることができる。There are no particular restrictions on the type or use of printing materials, and the photographic constituent layers of such silver halide photographic materials may contain chemical sensitizers such as hypo, noble metal sensitizers such as gold salts, platinum, etc. agents, contrast enhancing agents such as hexahalogenorhodium complexes, hexahalogenorhodium complexes, nucleic acid decomposition products, JP-A-50-14792δ, JP-A No. 51-107
Mercazoto heterocyclized metals, color sensitizers, stabilizers, antifouling agents, cazolers for color photography, hardening agents, non-diffusible sialium dihydroxyl 4-benzene compounds, hydroquinone as described in Onishikke No. 129. , Methyl High P■ Quinone, Phenidone and other halogenated scissors developing agents, coating aids, fogging agents, direct? It can contain additives for direct positive photographic emulsions such as dyes for dyes, dye developers, and physical development nuclei for photographic elements for fine powder transfer.
次に、本発明をさらに具体的に説明するために、実施例
を述べる。Next, examples will be described in order to explain the present invention more specifically.
〔実施6例1〕
第1表に示す配合の塗布組成物を下記のように調製した
。[Example 6 Example 1] A coating composition having the formulation shown in Table 1 was prepared as follows.
スチレン−無水マレイン酸共重合物の251水溶液(商
品名マ四ンM8−25、大同工業■製)80J9にコロ
イド状シリカの201水溶液(商品名スノーテックスC
1日産化学■製)315Iおよびlリビニルビロリドン
(商品名PvPK−90,ガフ(GAF)社製)のδチ
水溶液25.2g(この場合、コロイド状シリカ:ポリ
ビニルピロリPンの構成比率は1:0.02*%ある)
を添加する。更に、下式f示される化合物(1)の10
−メタノール溶液60ocおよびPデシルベンゼンスル
フォン酸ソーダのδチ水溶液14Iを添加する。その後
、水を加えて全量を1000IIに調製する(なお、比
較のために別途。A 251 aqueous solution of styrene-maleic anhydride copolymer (trade name Mafourin M8-25, manufactured by Daido Kogyo ■) 80J9 and a 201 aqueous solution of colloidal silica (trade name Snowtex C)
1 (manufactured by Nissan Chemical ■) 315I and 25.2 g of an aqueous solution of δ-chi of 1-rivinylpyrrolidone (trade name: PvPK-90, manufactured by GAF) (in this case, the composition ratio of colloidal silica: polyvinylpyrroli-P) is 1:0.02*%)
Add. Furthermore, 10 of the compound (1) represented by the following formula f
- Add 60 oc of methanol solution and 14 I of aqueous solution of sodium P-decylbenzenesulfonate. Then, add water to adjust the total volume to 1000II (separately for comparison).
コロイド状シリカおよび/lたは−り♂エルピロリPン
を添加しない塗布組成物を調製する)。A coating composition is prepared without the addition of colloidal silica and/or L pylori P).
このようにして調製された塗布組成物をノ々ツクコート
用塗布液として、予めコロナ放電処理を施し九−リエチ
レン被覆紙の裏面に、グ2ぜヤシ−ター1塗布量10バ
(湿分)f塗布して乾燥した。The coating composition thus prepared was used as a coating solution for Nonotsu Coat, and was coated on the back side of 9-polyethylene coated paper with a coating amount of 10% (moisture) f. Apply and dry.
使用されたぼりエチレン被覆紙は対ポリエチレン10重
量−の二酸化チタン、適量の分散剤および青味剤を含む
低密度ポリエチレン(顔料添加前のポリエチレンは密度
0.9211A、メルトインデックス5)をサイズ剤と
して対ノ々ルゾ0.4重量−のケテンダイマー、乾強度
剤として対ノルジ2重量−のカチオン化澱粉並びに対A
シフ1重量−のカル−キシ変性Iすeニルアルコール、
湿強度剤として対/ぐルプ0.4重量−のポリアミP/
リア之ン二一り四ルヒドリン樹脂および適量の螢光増白
剤を含有する広葉樹漂白クララトノ臂ルプと針葉樹漂白
サルファイドパルプの1:1混合ノ々ルゾから成る坪量
16011/dの写真用紙に予めコロナ放電処理した後
、厚さ30μにエクストルー−)VZン被覆し、−刃裏
面には低密FRがりエチレン(密度0.92シー、メル
トインデックスδ)と高密度−リエチレン(密度0.9
6シー、メルトインデックス)の1:1混合物を表面と
同様にエフストルーフ冒ン被覆したものである。を九、
ぼりエチレンの表面は、全く平担ないわゆるグ冒ツシー
面に、裏ばりエチレンの画質はマット面に加工したもの
マある。The used ethylene-coated paper is made of low-density polyethylene containing titanium dioxide (10% by weight of polyethylene), an appropriate amount of dispersant, and a blue tint (the polyethylene before adding pigment has a density of 0.9211A and a melt index of 5) as a sizing agent. 0.4 weight of ketene dimer for Norruzo, cationized starch of 2 weight for Nordi as a dry strength agent, and A
Schiff 1wt carboxy-modified Isenyl alcohol,
Polyamide P/glup 0.4 wt. as a wet strength agent
A photo paper with a basis weight of 16011/d consisting of a 1:1 mixture of hardwood bleached clarato pulp and softwood bleached sulfide pulp containing a 4-hydrohydrin resin and an appropriate amount of fluorescent whitening agent was prepared in advance. After corona discharge treatment, it is coated with extra-VZ to a thickness of 30μ, and the back side of the blade is coated with low-density FR polyethylene (density 0.92, melt index δ) and high-density polyethylene (density 0.9).
As with the surface, the surface was coated with a 1:1 mixture of 6C, Melt Index). nine,
The surface of the ethylene film is completely flat, so-called a greasy surface, while the image quality of the ethylene film with the back surface is that of a matte surface.
これらのI々ツクR−)層を塗設したぼりエチレン被覆
紙の表WKコ四す放電処理し九後、黄色カプラーを含む
塩臭化銀ゼラチン乳剤とその保護層をエクストルーク■
ン方式1塗布、乾燥してへ四ゲン化銀カラー写真材料を
作成した。The surface of the ethylene-coated paper coated with these layers was subjected to electrical discharge treatment, and then the silver chlorobromide gelatin emulsion containing the yellow coupler and its protective layer were extruded.
A silver tetragenide color photographic material was prepared by coating method 1 and drying.
/セック;−ト層用の塗布液の安定性は以下に記載の方
法で評価した。The stability of the coating solution for the /sec;-t layer was evaluated by the method described below.
〔/々ツク;−ト層期用塗布液安定性の評価〕各塗布液
を試験管に同一量採取して、40℃の恒温槽中″e1日
間保存後、塗液の状態を観察し、安定性を評価する。そ
の際、評価基準は・○印(&好)、Δ印(やや良好)、
x印(不可)1表示した。[Evaluation of stability of coating solution for layer stage] Take the same amount of each coating solution into a test tube, store it in a constant temperature bath at 40°C for 1 day, and then observe the condition of the coating solution. Evaluate the stability. At that time, the evaluation criteria are: ○ mark (& good), Δ mark (fairly good),
1 x mark (not allowed) was displayed.
また、以上のようにして得られ丸缶試料を50℃、60
引■の恒温恒湿槽に1日間保存した後以下に記載の方法
f評価した。その際、ノ々ツクコート層の帯電防止性能
の評価基準としては数値1、またバックコート層のme
加修性および写真性適性の評価基準としては、O印(良
好)Δ印(やや良好)、X印(不可)で表示し喪。In addition, the round can sample obtained as described above was heated at 50°C and 60°C.
After being stored in a constant temperature and humidity chamber for one day, it was evaluated using the method f described below. At that time, the evaluation standard for the antistatic performance of the Nonotsu coat layer is the value 1, and the me value of the back coat layer.
The evaluation criteria for retouchability and photographic suitability are indicated by O (good), Δ (slightly good), and X (unsatisfactory).
〔)々ツクコート層の帯電防止性能の評価〕、20℃、
35tIIIRHにおける試料の表面固有抵抗を1cm
の距離をおいて配置した長さlocmの電極を用いて測
定した。[Evaluation of the antistatic performance of the coating layer], 20°C,
The surface resistivity of the sample at 35tIIIRH is 1cm.
The measurements were made using electrodes with a length of locm placed at a distance of .
〔バックコート層の鉛瞭加鹸性の評価〕硬さの異りた鉛
筆f筆記を行い1表面の記録状態を観察し、有効性を判
定する。[Evaluation of the readability of the back coat layer] Write with pencils of different hardness, observe the recording state on the surface, and judge the effectiveness.
写真乳剤層とdツクブー1層面を重ね合わせてロール状
に巻き、50℃、80チRHの恒温恒湿槽に2日間保存
した彼、発色現像(30℃。The photographic emulsion layer and the dtsukbu 1 layer were overlapped, rolled into a roll, and stored in a constant temperature and humidity bath at 50°C and 80°RH for 2 days, followed by color development (30°C).
5分)、−浴漂白定着処理して、カブリ判定を行う。5 minutes), - Bath bleach-fix treatment and fog judgment.
得られた結果を第2表に示す。The results obtained are shown in Table 2.
第2表かられかるように、=ロイド状シリカのない塗布
層の場合(&(3)、Na(4))、塗布液の不安定性
は招来されないけれども、鉛線加筆性が不良で、帯電防
止性能が劣って問題1ある。As can be seen from Table 2, in the case of a coating layer without =roidal silica (&(3), Na(4)), instability of the coating solution is not caused, but the pencilability is poor and the electrification is poor. There is a problem with poor prevention performance.
またコ四イP状シリカがありても、ポリ−ニルt q
vP yf)lIRh塗布層(1’k(2) ) O場
合にハ、塗布液の安定性が不良1問題1ある。Also, even if there is P-type silica, poly-nyl tq
vP yf)lIRhCoating layer (1'k(2)) In the case of O, there is a problem with poor stability of the coating liquid.
しかしながら1本発明における塗布層(&(1) )は
、いずれの評価基準においても良好なる結果を示し、良
好な帯電防止性能、錯綜加筆性および写真性適性と共に
良好な塗液安定性を有する優れた塗布組成物であること
がよくわかる。However, the coating layer (&(1)) in the present invention shows good results in all evaluation criteria, and has excellent antistatic performance, good interwoven writing ability, photographic suitability, and good coating liquid stability. It can be clearly seen that this is a coating composition.
〔実施例2〕
実施例1の塗布液−1の配置において、第3表に記載の
コ四イド状シリカ:ポリビニルピ四りPンの構成比率に
なる様に、ポリビニルビ四9 )%ンの配合量を変化さ
せる以外は実施例1と同様に6爽施した。[Example 2] In the arrangement of coating liquid 1 of Example 1, the composition of polyvinyl vinyl silica (9)% was adjusted so that the composition ratio of cotetraid silica:polyvinyl vinyl pyriP was as shown in Table 3. Six coats were applied in the same manner as in Example 1 except that the amount was changed.
その結果、コロイド状シリカ:ポリピエルピロリryo
構成比率が1 : 0.001〜l:Oユ50′1%あ
る塗布組成物の安定性は曳好なもの1あったが、それ以
外の構成比率フある塗布組成物の安定性は不良11本発
明の有用性がよく理解される。As a result, colloidal silica: Polypier pylori ryo
The stability of coating compositions with a composition ratio of 1:0.001 to 1:050'1% was good1, but the stability of coating compositions with other composition ratios was poor11. The utility of the present invention is well understood.
第3表
実施例1において、ガフ(GAF)社製ポリビニルピロ
リドンPVP K−9Qの代わりに、同じメーカーのI
リビニルビロリドンPVPKべ幻、FVPK−■を用い
る以外は、実施例1と全く同様に実施した結果、実施例
1と同様の結果を得た。In Example 1 of Table 3, instead of polyvinylpyrrolidone PVP K-9Q manufactured by GAF, I
Example 1 was carried out in exactly the same manner as in Example 1, except that ribinylpyrrolidone PVPK Begen and FVPK-■ were used, and the same results as in Example 1 were obtained.
Claims (1)
ら構成されており、かつ(b);ロイP状シリカ: (
C)!1N、9♂ニルピロリドンの構成比率がl:cl
ool〜1:0.150であることを特徴とする塗布組
成物。It is composed of colloidal silica and (c) It is ♂ Nilze ■ Ridone, and (b); Roy P-like silica: (
C)! The composition ratio of 1N, 9♂nylpyrrolidone is l:cl
A coating composition characterized in that the ratio is ool~1:0.150.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14420581A JPS5845248A (en) | 1981-09-11 | 1981-09-11 | Coating composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14420581A JPS5845248A (en) | 1981-09-11 | 1981-09-11 | Coating composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5845248A true JPS5845248A (en) | 1983-03-16 |
JPH0116274B2 JPH0116274B2 (en) | 1989-03-23 |
Family
ID=15356663
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14420581A Granted JPS5845248A (en) | 1981-09-11 | 1981-09-11 | Coating composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5845248A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005132912A (en) * | 2003-10-29 | 2005-05-26 | Naoyuki Kato | Raw material for coating composition and coating composition using the same |
JP2005523981A (en) * | 2002-04-30 | 2005-08-11 | ハイドロマー インコーポレイテッド | Hydrophilic versatile coating composition |
JP2006131901A (en) * | 2004-10-12 | 2006-05-25 | Mitsubishi Polyester Film Gmbh | Water-borne coating composition, hydrophilic coated polyester film and method for producing the same |
-
1981
- 1981-09-11 JP JP14420581A patent/JPS5845248A/en active Granted
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005523981A (en) * | 2002-04-30 | 2005-08-11 | ハイドロマー インコーポレイテッド | Hydrophilic versatile coating composition |
JP2005132912A (en) * | 2003-10-29 | 2005-05-26 | Naoyuki Kato | Raw material for coating composition and coating composition using the same |
JP2006131901A (en) * | 2004-10-12 | 2006-05-25 | Mitsubishi Polyester Film Gmbh | Water-borne coating composition, hydrophilic coated polyester film and method for producing the same |
Also Published As
Publication number | Publication date |
---|---|
JPH0116274B2 (en) | 1989-03-23 |
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